aktualisiertes pdf - DPG-Tagungen
aktualisiertes pdf - DPG-Tagungen
aktualisiertes pdf - DPG-Tagungen
Erfolgreiche ePaper selbst erstellen
Machen Sie aus Ihren PDF Publikationen ein blätterbares Flipbook mit unserer einzigartigen Google optimierten e-Paper Software.
and require precise measurements with multiple tracers. UV-spectroscopy<br />
is introduced as a new technique for direct and fast measurements of<br />
multiple tracer concentrations both in the water and the atmosphere.<br />
Volatile aromatic hydrocarbons such as benzene, thiophene, pyridine and<br />
derivates and some other species can be measured. The new technique is<br />
attractive for two reasons: a) concentrations of volatile species dissolved<br />
in water can be measured directly in the water without the need for ex-<br />
UP 16 Poster: Atmosphäre<br />
traction and b) tracers with a wide range of physicochemical parameters,<br />
i.e. Schmidt number and solubility can be measured simultaneously so<br />
that a detailed experimental study of the influence of these parameters<br />
on air-water gas exchange becomes feasible. The experimental set up and<br />
analysis of the spectral data are described. First results from experiments<br />
in a 120cm diameter circular wind-wave-facility in Heidelberg show the<br />
significant potentiality of the new technique.<br />
Zeit: Dienstag 14:00–16:00 Raum: Schellingstr. 3<br />
UP 16.1 Di 14:00 Schellingstr. 3<br />
Advection, diffusion and reaction of pollutants in a two dimensional<br />
flow — •G. Bene 1 and H. Lustfeld 2 — 1 Institute for Theoretical<br />
Physics, Eötvös University, Pázmány Péter sétány 1/A, H-1117<br />
Budapest, Hungary, e-mail: bene@arpad.elte.hu — 2 Forschungszentrum<br />
Jülich, IFF, 52425 Jülich, e-mail: h.lustfeld@fz-juelich.de<br />
Advection, diffusion and reaction of pollutants in a two dimensional<br />
flow is studied. Two separate but related methods are considered:<br />
1) Effective diffusion and reaction rates based on a special (exact) solution<br />
are calculated and extended to the general case. We present results<br />
for the concentration distribution, the effective diffusion and effective reaction<br />
rates.<br />
2) In experimental situations the detailed structure of the concentration<br />
field is mostly not available, only a locally averaged concentration field ¯c<br />
is given. We derive an equation for ¯c directly. This approach is generalized<br />
for calculating effective reaction rates between two pollutants.<br />
UP 16.2 Di 14:00 Schellingstr. 3<br />
Measurement of CO, NO, NO2, Organic Compounds and<br />
PM10 at a Motorway Location in an Austrian Valley during<br />
a Twelve Hour Blockade Period — •Jonathan Beauchamp 1 ,<br />
Armin Wisthaler 1 , Wolfgang Grabmer 1 , Christian Neuner 2 ,<br />
Andreas Weber 2 , and Armin Hansel 1 — 1 Institut fuer Ionenphysik,<br />
Universitaet Innsbruck, Technikerstr. 25, A-6020 Innsbruck, Austria<br />
— 2 Landesforstdirektion Waldschutz/Luftguete, Amt der Tiroler<br />
Landesregierung, Buergerstr. 36, A-6020 Innsbruck, Austria<br />
UP 17 Poster: Atmosphäre und Messtechnik<br />
In-situ measurements of key chemical compounds took place over an<br />
eleven day period encompassing a twelve hour motorway blockade (25th<br />
October 2002, 12:00 noon to 24:00 midnight). Located within the Inn<br />
valley (Tirol, Austria), the monitoring site has restricted dilution conditions<br />
for air pollutants and high traffic sources. Continuous levels of CO,<br />
NO, NO2 and certain organic compounds were monitored and detection<br />
of PM10 was carried out. The period of traffic absence showed a dramatic<br />
decrease of NO. PM10, as well as the aromatics, showed a corresponding<br />
but slower decrease throughout this period.<br />
Analysis of data separated into weekdays and weekends showed significant<br />
reductions of NOx and PM10 at the weekend, when fewer heavy<br />
duty vehicles (HDV) use the motorway, implicating HDV as the dominant<br />
source of these two pollutants. Principal components analyses for<br />
the separated data further support this.<br />
Finally, our data clearly restate the dominating meteorological influence<br />
which cause severely restricted dispersion conditions for air pollutants<br />
in Alpine valleys.<br />
Zeit: Dienstag 14:00–16:00 Raum: Schellingstr. 3<br />
UP 17.1 Di 14:00 Schellingstr. 3<br />
HOx-Radikalkonzentrationen während der ECHO Feldmesskampagne<br />
im Sommer 2003 — •Manfred Siese 1 , Lutz Rupp 1 ,<br />
Andreas Hofzumahaus 1 , Jörg Kleffmann 2 , Djuro Mihelcic 1 ,<br />
Frank Holland 1 und Eric Schlosser 1 — 1 Institut für Chemie<br />
und Dynamik der Geosphäre II: Troposphäre, Forschungszentrum<br />
Jülich, Leo Brandt Strasse, 52425 Jülich — 2 Bergische Universität<br />
Gesamthochschule Wuppertal, Fachbereich 9, Physikalische Chemie,<br />
Gaußstr. 20, 42097 Wuppertal<br />
Mittels laser-induzierter Fluoreszenz (LIF) wurden im Sommer 2003<br />
im Rahmen des ECHO-Projektes in einem Mischwaldbestand OH−<br />
und HO2-Radikalkonzentrationen gemessen. Es wurde ein neues LIF-<br />
Instrument eingesetzt, welches kompakt und leicht genug war, um auf<br />
einer fahrbaren Plattform entlang eines 36 m hohen Turmes im Wald<br />
eingesetzt werden zu können. So konnten die HOx-Konzentrationen auf<br />
verschiedenen Höhen im und oberhalb des Waldbestandes bestimmt werden.<br />
Erstmals konnten bei dieser Kampagne vertikale Konzentrationsgradienten<br />
der HOx-Radikale zwischen 2 m bis 38 m gemessen werden. Es<br />
wurden mehrere HOx-Tagesgänge sowohl am Waldboden, als auch innerhalb<br />
und oberhalb des Kronenraumes aufgenommen. Dabei konnten OH<br />
und HO2-Radikale auch in der Nacht nachgewiesen werden.<br />
Die HO2-Radikalkonzentrationen wurden gleichzeitig mit Hilfe der<br />
Matrix-Isolation-Elektronen-Spin-Resonanz Technik (MIESR) bestimmt,<br />
wobei sich eine sehr gute Übereinstimmung mit den Ergebnissen aus LIF-<br />
Messungen ergab.<br />
163<br />
UP 17.2 Di 14:00 Schellingstr. 3<br />
Multi-axis DOAS observations of atmospheric trace gases at<br />
the Greenland ice cap — •Thomas Medeke, Sixten Fietkau,<br />
Annette Ladstaetter- Weissenmayer, Hilke Oetjen, Andreas<br />
Richter, Folkard Wittrock, and John Burrows — University of<br />
Bremen, IUP, Otto- Hahn- Allee 1, 28359 Bremen<br />
In July 2003 a new MAX- DOAS instrument has been installed at<br />
Summit (Greenland). MAX-DOAS is based on the well-known UV/VIS<br />
instruments, which use the sunlight scattered in the zenith sky as the<br />
light source and the method of Differential Optical Absorption Spectroscopy<br />
(DOAS) to derive column amounts of absorbers like ozone and<br />
nitrogen dioxide. Substantial enhancements have been applied to this<br />
standard setup to use different line of sights near to the horizon as additional<br />
light sources (MAX - multi axis). In addition, this measurement<br />
technique can be used for both ground based observations (e.g. Network<br />
for Detection of Stratospheric Change - NDSC) and validation of satellite<br />
instruments (e.g. Global Ozone Monitoring Experiment - GOME,<br />
Scanning Imaging Absorption Spectrometer for Atmospheric Chartography<br />
- SCIAMACHY) which allows to combine highly time and spatial<br />
resolved data of selected locations with data of global coverage. First results<br />
from measurements at the Summit part of the BREDOM (Bremian<br />
DOAS Network for Atmospheric Measurements) will be presented and interpreted<br />
with the full-spherical radiation transport model SCIATRAN.