Klaus-Peter Heue

Influence of the 2008 Kasatochi volcanic eruption on sulfurous and carbonaceous aerosol constituents in the lower stratosphere

Influences on stratospheric aerosol during the first four months following the eruption of Kasatochi volcano (Alaska) were studied using observations at 10700 +/- 600 m altitude from the CARIBIC platform. Collected aerosol samples were analyzed for elemental constituents. Particle number concentrations were recorded in three size intervals together with ozone mixing ratios and slant column densities of SO2. The eruption increased particulate sulfur concentrations by a factor of up to 10 compared to periods before the eruption (1999-2002 and 2005-August 2008). Three to four months later, the concentration was still elevated by a factor of 3 in the lowermost stratosphere at northern midlatitudes. Besides sulfur, the Kasatochi aerosol contained a significant carbonaceous component and ash that declined in time after the eruption. The carbon-to-sulfur mass concentration ratio of the volcanic aerosol was 2.6 seven days after the eruption and reached 1.2 after 3 - 4 months. Citation: Martinsson, B. G., C. A. M. Brenninkmeijer, S. A. Carn, M. Hermann, K.-P. Heue, P. F. J. van Velthoven, and A. Zahn (2009), Influence of the 2008 Kasatochi volcanic eruption on sulfurous and carbonaceous aerosol constituents in the lower stratosphere, Geophys. Res. Lett., 36, L12813, doi: 10.1029/2009GL038735. (Less)

Retrieval of profile information from airborne multiaxis UV-visible skylight absorption measurements

A recent development in ground-based remote sensing of atmospheric constituents by UV-visible absorption measurements of scattered light is the simultaneous use of several horizon viewing directions in addition to the traditional zenith-sky pointing. The different light paths through the atmosphere enable the vertical distribution of some atmospheric absorbers, such as NO2, BrO, or O3, to be retrieved. This approach has recently been implemented on an airborne platform. This novel instrument, the airborne multiaxis differential optical absorption spectrometer (AMAXDOAS), has been flown for the first time. In this study, the amount of profile information that can be retrieved from such measurements is investigated for the trace gas NO2. Sensitivity studies on synthetic data are performed for a variety of representative measurement conditions including two wavelengths, one in the UV and one in the visible, two different surface spectral reflectances, various lines of sight (LOSs), and for two different flight altitudes. The results demonstrate that the AMAXDOAS measurements contain useful profile information, mainly at flight altitude and below the aircraft. Depending on wavelength and LOS used, the vertical resolution of the retrieved profiles is as good as 2 km near flight altitude. Above 14 km the profile information content of AMAXDOAS measurements is sparse. Airborne multiaxis measurements are thus a promising tool for atmospheric studies in the troposphere and the upper troposphere and lower stratosphere region.

Direct observation of two dimensional trace gas distributions with an airborne Imaging DOAS instrument

In many investigations of tropospheric chemistry information about the two dimensional distribution of trace gases on a small scale (e.g. tens to hundreds of metres) is highly desirable. An airborne instrument based on imaging Differential Optical Absorption Spectroscopy has been built to map the two dimensional distribution of a series of relevant trace gases including NO 2, HCHO, C2H2O2, H2O, O4, SO2, and BrO on a scale of 100 m. Here we report on the first tests of the novel aircraft instrument over the industrialised South African Highveld, where large variations in NO2 column densities in the immediate vicinity of several sources e.g. power plants or steel works, were measured. The observed patterns in the trace gas distribution are interpreted with respect to flux estimates, and it is seen that the fine resolution of the measurements allows separate sources in close proximity to one another to be distinguished.

Spatial and temporal variations in NO2 distributions over Beijing, China measured by imaging differential optical absorption spectroscopy

During the CAREBEIJING campaign in 2006, imaging differential optical absorption spectroscopy (I-DOAS) measurements were made from 08:00 to 16:00 on September 9 and 10 over Beijing, China. Detailed images of the near-surface NO(2) differential slant column density (DSCD) distribution over Beijing were obtained. Images with less than a 30-min temporal resolution showed both horizontal and vertical variations in NO(2) distributions. For DSCD to mixing ratio conversion, path length along the lines of I-DOAS lines of sight was estimated using the light-extinction coefficient and Angstrom exponent data obtained by a transmissometer and a sunphotometer, respectively. Mixing ratios measured by an in-situ NO(2) analyzer were compared with those estimated by the I-DOAS instrument. The obtained temporal and spatial variations in NO(2) distributions measured by I-DOAS for the two days are interpreted with consideration of the locations of the major NO(x) sources and local wind conditions. I-DOAS measurements have been applied in this study for estimating NO(2) distribution over an urban area with multiple and distributed emission sources. Results are obtained for estimated temporal and spatial NO(2) distributions over the urban atmosphere; demonstrating the capability of the I-DOAS technique. We discuss in this paper the use of I-DOAS measurements to estimate the NO(2) distribution over an urban area with multiple distributed emission sources.

CARIBIC aircraft measurements of Eyjafjallajökull volcanic plumes in April/May 2010

The Civil Aircraft for the Regular Investigation of the Atmosphere Based on an Instrument Container (CARIBIC) project investigates physical and chemical processes in the Earth’s atmosphere using a Lufthansa Airbus long-distance passenger aircraft. After the beginning of the explosive eruption of the Eyjafjallaj ökull volcano on Iceland on 14 April 2010, the first CARIBIC volcano-specific measurement flight was carried out over the Baltic Sea and Southern Sweden on 20 April. Two more flights followed: one over Ireland and the Irish Sea on 16 May and the other over the Norwegian Sea on 19 May 2010. During these three special mission flights the CARIBIC container proved its merits as a comprehensive flying laboratory. The elemental composition of particles collected over the Baltic Sea during the first flight (20 April) indicated the presence of volcanic ash. Over Northern Ireland and the Irish Sea (16 May), the DOAS system detected SO 2 and BrO co-located with volcanic ash particles that increased the aerosol optical depth. Over the Norwegian Sea (19 May), the optical particle counter detected a strong increase of particles larger than 400 nm diameter in a region where ash clouds were predicted by aerosol dispersion models. Aerosol particle samples collected over the Irish Sea and the Norwegian Sea showed large relative enhancements of the elements silicon, iron, titanium and calcium. Non-methane hydrocarbon concentrations in whole air samples collected on 16 and 19 May 2010 showed a pattern of removal of several hydrocarbons that is typical for chlorine chemistry in the volcanic clouds. Comparisons of measured ash concentrations and simulations with the FLEXPART dispersion model demonstrate the difficulty of detailed volcanic ash dispersion modelling due to the large variability of the volcanic cloud sources, extent and patchiness as well as the thin ash layers formed in the volcanic clouds.

Airborne imaging differential optical absorption spectroscopy: Trace-gas measurements from the suburbs to the sub-continent

A remote sensing instrument for high-resolution measurement of two dimensional trace-gas distributions from an aircraft has been built. The instrument has been tested during three measurement campaigns over the South African High-veld region. The resolution achieved is less than 100 metres, allowing point sources to be clearly identified. Measurements have been interpreted with respect to emission flux and oxidation of species in the atmosphere. The high speed of the aircraft also allows measurements to be made on a regional scale.

Two- and Three Dimensional Observation of Trace Gas and Aerosol Distributions by DOAS Techniques

Spatially resolved measurements of trace gas abundances by satellite have revolutionised the field of large-scale tropospheric chemistry observation and modelling during recent years. Now a similar revolution is imminent on local and regional scales. A key role in these advances is played by spatially resolving spectroscopic techniques like active and passive – DOAS tomographic measurements of two-dimensional trace gas distributions, as well as ground based and airborne Imaging DOAS (I-DOAS) observation of 2D- and 3D- trace gas patterns. A particularly promising approach is the combination of tomographic techniques with imaging – DOAS on airborne platforms, which can provide three-dimensional trace gas distributions. While satellite-based 2D – mapping of trace gas distributions is now in widespread use for global and regional investigations aircraft based instruments allow complementary studies at much higher spatial resolution (tens of meters instead of tens of km). Since state of the art instruments can be employed rather than technology from the last decade (which is dictated by reliability requirements and long lead times of satellite experiments) novel approaches like tomographic techniques or Short-Wave Infra-Red (SW-IR) observations can be applied. Technological approaches and sample results are discussed.