ALBERT

Beschreibung: The volatile and hygroscopic properties of ammonium sulphate seeded and un-seeded secondary organic aerosol (SOA) derived from the photo-oxidation of atmospherically relevant concentrations of α-pinene were studied. The seed particles were electrospray generated ammonium sulphate ((NH4)2SO4) having diameters of approximately 33 nm with a quasi-mono-disperse size distribution (geometric standard deviation σg=1.3). The volatile and hygroscopic properties of both seeded and unseeded SOA were simultaneously measured with a VH-TDMA (volatility – hygroscopicity tandem differential mobility analyzer). VH-TDMA measurements of unseeded SOA show a decrease in the hygroscopic growth (HGF) factor for increased volatilisation temperatures such that the more volatile compounds appear to be more hygroscopic. This is opposite to the expected preferential evaporation of more volatile but less hygroscopic material, but could also be due to enhanced oligomerisation occurring at the higher temperature in the thermodenuder. In addition, HGF measurements of seeded SOA were measured as a function of time at two relative humidities, below (RH 75%) and above (RH 85%) the deliquescence relative humidity (DRH) of the pure ammonium sulphate seeds. As these measurements were conducted during the onset phase of photo-oxidation, during particle growth, they enabled us to find the dependence of the HGF as a function of the volume fraction of the SOA coating. HGF's measured at RH of 85% showed a continuous decrease as the SOA coating thickness increased. The measured growth factors show good agreements with ZSR predictions indicating that, at these RH values, there are only minor solute-solute interactions. At 75% RH, as the SOA fraction increased, a rapid increase in the HGF was observed indicating that an increasing fraction of the (NH4)2SO4 is subject to a phase transition, going into solution, with an increasing volume fraction of SOA. To our knowledge this is the first time that SOA derived from photo-oxidised α-pinene has been shown to affect the equilibrium water content of inorganic aerosols below their DRH. For SOA volume fractions above ~0.3 the measured growth factor followed roughly parallel to the ZSR prediction based on fully dissolved (NH4)2SO4 although with a small difference that was just larger than the error estimate. Both incomplete dissolution and negative solute-solute interactions could be responsible for the lower HGF observed compared to the ZSR predictions.

Beschreibung: In this paper, we present measurements of total and tropospheric ozone, retrieved from infrared radiance spectra recorded by the Infrared Atmospheric Sounding Interferometer (IASI), which was launched on board the MetOp-A European satellite in October 2006. We compare the IASI total ozone columns to observations from the Global Ozone Monitoring Experiment-2 (GOME-2) for one full year of observations (2008). The global distributions are in good agreement, with a correlation coefficient better than 0.9. On average, IASI ozone retrievals exhibit a positive bias compared to GOME-2 of about 4.9 DU (2.9%) to 13 DU (4.4%) depending on the season. In addition to total ozone columns, the good spectral resolution of IASI enables the retrieval of tropospheric ozone concentrations. Comparisons of IASI tropospheric columns to 490 collocated ozone soundings available from several stations around the globe have been performed for the period June 2007–August 2008. IASI tropospheric ozone columns compare well with sonde observations, with correlation coefficients of 0.95 and 0.77 for the [surface – 6 km] and [surface – 12 km] partial columns, respectively. IASI retrievals tend to overestimate the tropospheric ozone columns in comparison with ozonesonde measurements. Positive average biases of 0.15 DU (1.2%) and 3 DU (11%) are found for the [surface – 6 km] and for the [surface – 12 km] partial columns, respectively.

Beschreibung: The volatile and hygroscopic properties of ammonium sulphate seeded and unseeded secondary organic aerosol (SOA) derived from the photo-oxidation of atmospherically relevant concentrations of α-pinene were studied. The seed particles were electrospray generated ammonium sulphate ((NH4)2SO4) having diameters of approximately 33 nm with a quasi-mono-disperse size distribution (geometric standard deviation σg=1.3). The volatile and hygroscopic properties of both seeded and unseeded SOA were simultaneously measured with a VH-TDMA (volatility – hygroscopicity tandem differential mobility analyzer). VH-TDMA measurements of unseeded SOA show a decrease in the hygroscopic growth (HGF) factor for increased volatilisation temperatures such that the more volatile compounds appear to be more hygroscopic. This is opposite to the expected preferential evaporation of more volatile but less hygroscopic material, but could also be due to enhanced oligomerisation occurring at the higher temperature in the thermodenuder. In addition, HGF measurements of seeded SOA were measured as a function of time at two relative humidities, below (RH 75%) and above (RH 85%) the deliquescence relative humidity (DRH) of the pure ammonium sulphate seeds. As these measurements were conducted during the onset phase of photo-oxidation, during particle growth, they enabled us to find the dependence of the HGF as a function of the volume fraction of the SOA coating. HGF's measured at RH of 85% showed a continuous decrease as the SOA coating thickness increased. The measured growth factors show good agreements with ZSR predictions indicating that, at these RH values, there are only minor solute-solute interactions. At 75% RH, as the SOA fraction increased, a rapid increase in the HGF was observed indicating that an increasing fraction of the (NH4)2SO4 is subject to a phase transition, going into solution, with an increasing volume fraction of SOA. To our knowledge this is the first time that SOA derived from photo-oxidised α-pinene has been shown to affect the equilibrium water content of inorganic aerosols below their DRH. For SOA volume fractions above ~0.3 the measured growth factor followed roughly parallel to the ZSR prediction based on fully dissolved (NH4)2SO4 although with a small difference that was just larger than the error estimate. Both incomplete dissolution and negative solute-solute interactions could be responsible for the lower HGF observed compared to the ZSR predictions.

Beschreibung: In this paper, we present measurements of total and tropospheric ozone, retrieved from infrared radiance spectra recorded by the Infrared Atmospheric Sounding Interferometer (IASI), which was launched on board the MetOp-A European satellite in October 2006. We compare IASI total ozone columns to Global Ozone Monitoring Experiment-2 (GOME-2) observations and ground-based measurements from the Dobson and Brewer network for one full year of observations (2008). The IASI total ozone columns are shown to be in good agreement with both GOME-2 and ground-based data, with correlation coefficients of about 0.9 and 0.85, respectively. On average, IASI ozone retrievals exhibit a positive bias of about 9 DU (3.3%) compared to both GOME-2 and ground-based measurements. In addition to total ozone columns, the good spectral resolution of IASI enables the retrieval of tropospheric ozone concentrations. Comparisons of IASI tropospheric columns to 490 collocated ozone soundings available from several stations around the globe have been performed for the period of June 2007–August 2008. IASI tropospheric ozone columns compare well with sonde observations, with correlation coefficients of 0.95 and 0.77 for the [surface–6 km] and [surface–12 km] partial columns, respectively. IASI retrievals tend to overestimate the tropospheric ozone columns in comparison with ozonesonde measurements. Positive average biases of 0.15 DU (1.2%) and 3 DU (11%) are found for the [surface–6 km] and for the [surface–12 km] partial columns respectively.

Beschreibung: Peroxy radical measurements made on board the DLR-Falcon research aircraft over West Africa within the African Monsoon Multidisciplinary Analysis (AMMA) campaign during the 2006 wet monsoon are presented in this study. The analysis of data focuses on the photochemical activity of air masses sampled during episodes of intense convection and biomass burning. Generally, the total sum of peroxy radical mixing ratios, measured in the outflow of convective clouds, are quite variable but occasionally are coupled with the NO variations indicating the coexistence or simultaneous emission of NOx, with a potential radical precursor (i.e. formaldehyde, acetone or peroxides), which has likely been transported to higher atmospheric altitudes. Based on the measurements, significant O3 production rates around 1 ppb/h in the MCS outflow are estimated by using a box model with simplified chemistry. Peroxy radicals having mixing ratios around 20–25 pptv and with peak values of up to 60–70 pptv are measured within biomass burning plumes, detected at the coast in Ghana. Calculations of back-trajectory densities confirm the origin of these air masses being a biomass burning region at southern latitudes and close to the Gulf of Guinea, according to satellite pictures. Measured peroxy radical concentrations agree reasonably with modelled estimations taking into account simple local chemistry. Moreover, the vertical profiles taken at the aircraft base in Ouagadougou, Burkina Faso, indicate the common feature of having maximum concentrations between 2 and 4 km, in agreement with other literature values obtained under similar conditions.

Beschreibung: This presentation concentrates on solar occultation measurements with the spaceborne spectrometer SCIAMACHY in the UV-Vis wavelength range. Solar occultation measurements provide unique information about the vertical distribution of atmospheric constituents. For retrieval of vertical trace gas concentration profiles, an algorithm has been developed based on the optimal estimation method. The forward model is capable of simulating the extinction signals of different species as they occur in atmospheric transmission spectra obtained from occultation measurements. Furthermore, correction algorithms have been implemented to address shortcomings of the tangent height pre-processing and inhomogeneities of measured solar spectra. First results of O3 and NO2 vertical profile retrievals have been validated with data from ozone sondes and satellite based occultation instruments. The validation shows very promising results for SCIAMACHY O3 and NO2 values between 15 to 35km with errors of the order of 10% and 15%, respectively.

Beschreibung: Flood risk assessment is an essential part of flood risk management. As part of the new EU flood directive it is becoming increasingly more popular in European flood policy. Particularly cities with a high concentration of people and goods are vulnerable to floods. This paper introduces the adaptation of a novel method of multicriteria flood risk assessment, that was recently developed for the more rural Mulde river basin, to a city. The study site is Leipzig, Germany. The "urban" approach includes a specific urban-type set of economic, social and ecological flood risk criteria, which focus on urban issues: population and vulnerable groups, differentiated residential land use classes, areas with social and health care but also ecological indicators such as recreational urban green spaces. These criteria are integrated using a "multicriteria decision rule" based on an additive weighting procedure which is implemented into the software tool FloodCalc urban. Based on different weighting sets we provide evidence of where the most flood-prone areas are located in a city. Furthermore, we can show that with an increasing inundation extent it is both the social and the economic risks that strongly increase.

Beschreibung: Norddeutschland und angrenzende Gebiete, beeinflusst durch die skandinavischen Inlandvereisungen, sind klassische Regionen der Quartärgeologie und -stratigraphie. Der Schweizer Geologe VON MORLOT (1844) vermutete bereits, dass die nordischen Vergletscherungen das Erzgebirge in Sachsen erreicht haben könnten. Die Entdeckung der Gletscherschrammen auf triassischem Muschelkalk in Rüdersdorf bei Berlin durch TORRELL (1875) führte zur generellen Akzeptanz der Glazialtheorie in Deutschland. PENCK (1879) vermutete, dass Norddeutschland durch drei voneinander getrennte Vergletscherungen beeinflusst wurde. Die Kartierung der pleistozänen Ablagerungen durch den Preussischen Geologischen Dienst seit 1910 war ein Meilenstein für die Quartärstratigraphie, und die Begriffe „Elster“, „Saale“ und „Weichsel“ wurden in die wissenschaftliche Literatur eingeführt. Quartärgeologen wie L. SIEGERT, W. WEISSERMEL, K. KEILHACK, R. GRAHMANN und P. WOLDSTEDT beschrieben bereits Anfang des 20. Jahrhunderts fundamentale Zusammenhänge der Glazialgeschichte des nordmitteleuropäischen Tieflandes und ihre Korrelation mit fluvialen Prozessen. Die Quartärstratigraphie in Norddeutschland besitzt nicht zuletzt durch das dichte Netz an Bohrungen und durch die gut untersuchten Profilaufschlüsse in den Braunkohlentagebauen eine solide Basis. Von besonderer Bedeutung für die Stratigraphie ist in diesem Gebiet die Verzahnung von glaziärer und periglaziärer Fazies, d.h. die Beziehung zwischen Schotterterrassen, Moränenablagerungen und überdies zwischengeschalteten Interglazialsedimenten. In ihrer vertikalen Abfolge folgen sie in klassischer Weise dem stratigraphischen Grundgesetz.

Beschreibung: Von verschiedener Seite unternommene Korrelations-Versuche zum Saale-Komplex in Norddeutschland sind der Anlass, erneut die Stratigraphie dieses Zeitraums aus niedersächsischer Sicht darzustellen. Da das Holstein-Interglazial der Typus-Bohrung Bossel kürzlich mit der Th/U- Methode in Tiefsee-Stufe 9 datiert wurde, kommen für die jüngeren Thermomere Schöningen und Reinsdorf die Abschnitte 9a bis 7 in Frage. Die Speere aus dem Reinsdorf sind daher auf rund 270 000 - 240 000 Jahre zu veranschlagen. Die durch drei Eisvorstöße gegliederte saaleeiszeitliche Glaziärfolge wird kurz charakterisiert. Bisher unpublizierte Leitgeschiebezählungen aus SW-Niedersachsen werden vorgestellt; zusammen mit Aufschlussuntersuchungen und Kartierungen lassen sich daraus keine weiteren Unterteilungen des Haupt-Drenthe-Stadiums ableiten. Der zweite Saale-Vorstoß („Jüngere Drenthe") sollte aus stratigraphischen und petrographischen Gründen nicht zum Warthe-Stadium gestellt werden. Letzteres ist durch ein ostbaltisches Geschiebespektrum charakterisiert und mit den jeweils jüngsten saalezeitlichen Vorstößen der Nachbarländer zu korrelieren. Warmzeitliche organogene Sedimente zwischen den Eisvorstößen fehlen und sind aufgrund der geologischen Situation unwahrscheinlich.