ALBERT

Description: Chlorine dioxide, OClO, column amounts retrieved from measurements of the SCIAMACHY satellite instrument are presented and validated by comparison with simultaneous ground-based DOAS observations. In addition, the measurements are compared to model calculations taking into account the photochemical change along the light path. Although OClO does not participate directly in the destruction of ozone, its accurate measurement as well as modelling is crucial to understand the highly perturbed chlorine chemistry in the polar vortices. SCIAMACHY OClO slant columns retrieved during spring 2005 have been quantitatively validated by comparison with slant columns retrieved from measurements made in Ny-Ålesund (79° N, 12° E), Summit (73° N, 38° W) and Bremen (53° N, 9° E). Overall, good agreement is found. OClO slant column densities modelled with a set of stacked box models and considering the light path through the atmosphere are also included in this comparison. The model predictions differ significantly from the measured quantities. OClO amounts are underestimated for conditions of strong chlorine activation and at large solar zenith angles. Sensitivity studies for several parameters in the stacked box model have been performed and it is inferred that using the chemistry known to date, the observed OClO cannot be adequately reproduced within the range of uncertainties given for the various model parameters.

Description: A new approach to derive tropospheric concentrations of some atmospheric trace gases from ground-based UV/vis measurements is described. The instrument, referred to as the MAX-DOAS, is based on the well-known UV/vis instruments, which use the sunlight scattered in the zenith sky as the light source and the method of Differential Optical Absorption Spectroscopy (DOAS) to derive column amounts of absorbers like ozone and nitrogen dioxide. Substantial enhancements have been applied to this standard setup to use different lines of sight near to the horizon as additional light sources (MAX - multi axis). Results from measurements at Ny-Ålesund (79° N, 12° E) are presented and interpreted with the full-spherical radiative transfer model SCIATRAN. In particular, measurements of the oxygen dimer O4 which has a known column and vertical distribution in the atmosphere are used to evaluate the sensitivity of the retrieval to parameters such as multiple scattering, solar azimuth, surface albedo and refraction in the atmosphere and also to validate the radiative transfer model. As a first application, measurements of NO2 emissions from a ship lying in Ny-Ålesund harbour are presented. The results of this study demonstrate the feasibility of long term UV/vis multi axis measurement that can be used to derive not only column amounts of different trace gases but also some information on the vertical location of these absorbers.

Description: Chlorine dioxide, OClO, column amounts retrieved from measurements of the SCIAMACHY satellite instrument are presented and validated by comparison with simultaneous ground-based DOAS observations. In addition, the measurements are compared to model calculations taking into account the photochemical change along the light path. Although OClO does not participate directly in the destruction of ozone, its accurate measurement as well as modelling is crucial to understand the highly perturbed chlorine chemistry in the polar vortices. SCIAMACHY OClO slant columns retrieved during spring 2005 have been quantitatively validated by comparison with slant columns retrieved from measurements made in Ny-Ålesund (79° N, 12° E) and Summit (73° N, 38° W) as well qualitatively for Bremen (53° N, 9° E). Fair to good agreement is found depending on location as well as time of year. OClO slant column densities modelled with a set of stacked box models and considering the light path through the atmosphere are also included in this comparison. The model predictions differ significantly from the measured quantities. OClO amounts are underestimated for conditions of strong chlorine activation and at large solar zenith angles. Sensitivity studies for several parameters in the stacked box model have been performed and it is inferred that using the chemistry known to date, the observed OClO cannot be adequately reproduced within the range of uncertainties given for the various model parameters.

Description: Ground based observations of stratospheric and tropospheric bromine monoxide, BrO, from a multi axial differential optical absorption spectrometer, MAXDOAS, located at the UNEP/UNON site in Nairobi (1° S, 36° E) are presented for the year 2003. Differences in BrO slant column densities at 90° and 80° solar zenith angle retrieved from the zenith-sky measurements are used to study stratospheric BrO. They show only small variations with season, as expected for the small seasonality in stratospheric Bry and NO2 in this region. A pronounced diurnal variation can be observed, the average value for the morning being 1.3×1014 molecules/cm2 and for the evening 1.5×1014 molecules/cm2. The measurements are compared with simulations from a one-dimensional photochemical stacked box model which is coupled with a radiative transfer model to allow direct comparisons between the observations and the model calculations. In general the model reproduces the measurements very well. The differences in the absolute values are 15% for the evening and 20% for the morning which is within the limits of the combined uncertainties. Both seasonality and diurnal variation are well reproduced by the model. A sensitivity study shows that inclusion of the reaction BrONO2 + O(3P) significantly improves the agreement between model calculations and measurements, indicating an important role of this reaction in the stratosphere near to the equator. Tropospheric BrO columns and profile information is derived from the combined results obtained in the different viewing directions for the average over several clear days. The resulting tropospheric BrO columns are in the range of 4–7.5×1012 molecules/cm2 which is significant but lower than in previous studies at mid and high latitudes. The vertical distribution of the tropospheric BrO peaks at about 3 km indicating the absence of local sources at this high altitude site.

Description: A new approach to derive tropospheric concentrations of some atmospheric trace gases from ground-based UV/vis measurements is described. The instrument, referred to as the MAX-DOAS, is based on the well-known UV/vis instruments, which use the sunlight scattered in the zenith sky as the light source and the method of Differential Optical Absorption Spectroscopy (DOAS) to derive column amounts of absorbers like ozone and nitrogen dioxide. Substantial enhancements have been applied to this standard setup to use different lines of sight near to the horizon as additional light sources (MAX – multi axis). Results from measurements at Ny-Ålesund (79° N, 12° E) are presented and interpreted with the full-spherical radiation transport model SCIATRAN. In particular, measurements of the oxygen dimer O4 which has a known column and vertical distribution in the atmosphere are used to evaluate the sensitivity of the retrieval to parameters such as multiple scattering, solar azimuth, surface albedo and refraction in the atmosphere and also to validate the radiative transport model. As a first application, measurements of NO2 emissions from a ship lying in Ny-Ålesund harbour are presented. The results of this study demonstrate the feasibility of long term UV/vis multi axis measurement that can be used to derive not only column amounts of different trace gases but also some information on the vertical location of these absorbers.