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Featured researches published by N. Glatthor.


Journal of Quantitative Spectroscopy & Radiative Transfer | 2002

Sensitivity of trace gas abundances retrievals from infrared limb emission spectra to simplifying approximations in radiative transfer modelling

Gabriele P. Stiller; Thomas von Clarmann; B. Funke; N. Glatthor; F. Hase; M. Höpfner; A. Linden

The accuracy of trace gas abundances retrieved from spectrally resolved infrared limb emission measurements relies, among other things, on the appropriate modelling of radiative transfer through the actual atmosphere. We quantify the mapping of several commonly applied simplifications in radiative transfer modelling on the trace gas abundances retrieval error at the example of the Michelson interferometer for passive atmospheric sounding (MIPAS)/environmental satellite (ENVISAT) space borne Fourier transform infra-red limb emission experiment. The Karlsruhe optimized and precise radiative transfer algorithm (KOPRA) which was used as a tool for this study will be introduced. KOPRA supports accurate modelling of the particular instrument requirements of MIPAS and the observation scenarios during the ENVISAT mission, in particular with respect to its viewing direction and its altitude coverage of the atmosphere. We show that disregarding of horizontal temperature inhomogeneities and non-local thermodynamic equilibrium effects, insufficient accuracy in modelling of field-of-view and apodisation effects, and disregarding individual profiles of isotopic species play the key roles in radiative transfer modelling and lead to systematic retrieval errors which can by far exceed the expected random retrieval error caused by measurement noise.


Journal of the Atmospheric Sciences | 2005

Mixing Processes during the Antarctic Vortex Split in September–October 2002 as Inferred from Source Gas and Ozone Distributions from ENVISAT–MIPAS

N. Glatthor; T. von Clarmann; H. Fischer; B. Funke; U. Grabowski; M. Höpfner; S. Kellmann; M. Kiefer; A. Linden; M. Milz; T. Steck; G. P. Stiller; G. Mengistu Tsidu; Ding-Yi Wang

Abstract In late September 2002, an Antarctic major stratospheric warming occurred, which led to a strong distortion of the southern polar vortex and to a split of its mid- and upper-stratospheric parts. Such an event had never before been observed since the beginning of regular Antarctic stratospheric temperature observations in the 1950s. The split is studied by means of nonoperational level-2 CH4, N2O, CFC-11, and O3 data, retrieved at the Institute for Meteorology and Climate Research Karlsruhe (IMK) from high-resolution atmospheric limb emission spectra from the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) on board the European research satellite, Environmental Satellite (ENVISAT). Retrieved horizontal and vertical distributions of CH4 and N2O show good consistency with potential vorticity fields of the European Centre for Medium-Range Weather Forecasts (ECMWF) analysis for the entire period under investigation, even for fine structures such as vortex filaments. Tracer correlatio...


Journal of Geophysical Research | 2005

An enhanced HNO3 second maximum in the Antarctic midwinter upper stratosphere 2003

G. P. Stiller; Gizaw Mengistu Tsidu; T. von Clarmann; N. Glatthor; M. Höpfner; S. Kellmann; A. Linden; R. Ruhnke; H. Fischer; M. López-Puertas; B. Funke; S. Gil-López

Vertical profiles of stratospheric HNO 3 were retrieved from limb emission spectra recorded by the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) aboard the Envisat research satellite during the Antarctic winter 2003. A high second maximum of HNO 3 was found around 34 km altitude with abundances up to 14 ppbv HNO 3 during July. Similar high abundances have not been reported in the literature for previous winters, but for the subsequent Arctic winter 2003/2004, after severe perturbations due to solar proton events. The second HNO 3 maximum in the Antarctic stratosphere started to develop in early June 2003, reached peak values during July 2003, and decreased to about 7 ppbv at the end of August while being continuously transported downward before finally forming a single HNO 3 layer over all latitudes in the lower stratosphere together with the out-of-vortex primary HNO 3 maximum. The HNO 3 decrease in August 2003 was correlated with photochemical buildup of other NO v species as ClONO 2 and NO x . From the time scales observed, it can be ruled out that the 2003 long-term HNO 3 enhancements were caused by local gas phase reactions immediately after the solar proton event on 29 May 2003. Instead, HNO 3 was produced by ion cluster chemistry reactions and/or heterogeneous reactions on sulfate aerosols via N 2 O 5 from high amounts of NOy being continuously transported downward from the lower thermosphere during May to August.


Remote Sensing of Clouds and the Atmosphere VII | 2003

Remote sensing of the middle atmosphere with MIPAS

Thomas von Clarmann; Theo Chidiezie Chineke; Herbert Fischer; B. Funke; M. García-Comas; S. Gil-López; N. Glatthor; U. Grabowski; Michael Hoepfner; S. Kellmann; Michael Kiefer; A. Linden; M. López-Puertas; Miguel Angel Lopez-Valverde; Gizaw Mengistu Tsidu; Mathias Milz; Tilman Steck; Gabriele P. Stiller

On 1 March 2002 the Envisat research satellite has been launched successfully into its sun-synchronous orbit. One of its instruments for atmospheric composition sounding is the Michelson Interferometer for Passive Atmospheric Sounding, a limb-scanning mid-infrared Fourier transform spectrometer. Different scientific objectives of data users require different approaches to data analysis, which are discussed. A strategy on how to validate the involved algorithms and relevant strategies is presented.


Journal of Geophysical Research | 1995

The variability of ClONO2 and HNO3 in the Arctic polar vortex : comparison of Transall Michelson interferometer for passive atmospheric sounding measurements and three-dimensional model results

M. P. Chipperfield; J. A. Pyle; C. E. Blom; N. Glatthor; M. Höpfner; T. Gulde; C. Piesch; P. Simon

A three-dimensional radiative-dynamical-chemical model has been used to investigate measurements of column ClONO2 and HNO3 made by the airborne Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) instrument. MIPAS made measurements from the Transall aircraft in the northern hemisphere lower stratosphere from December 1992 to March 1993. The three-dimensional model has a detailed stratospheric chemistry scheme including heterogeneous reactions on polar stratospheric clouds and sulfate aerosols. The circulation in the model is specified from the European Centre for Medium Range Weather Forecasts analyses. The MIPAS measurements reveal large variability in column ClONO2 at the edge of the polar vortex. For the measurements of January 27 and 31, 1993, the model experiments show that variability in ClONO2 observed over this period can be explained by polar stratospheric cloud processing and recovery. Measurements of ClONO2 on February 2, 1993, showed large variations depending on the orientation of the aircraft relative to the edge of the vortex. Results from the model show that this is qualitatively consistent with the aircraft flying near to the collar region with its associated strong horizontal gradients of ClONO2. The models ability to simulate these strong gradients is limited by its relatively coarse resolution. In early March the vortex became very distorted. During this period MIPAS measured very large values of ClONO2 at high latitudes within the vortex but lower, although still large, values in the more southerly regions of the vortex. At this stage of the winter ClONO2 is the major chlorine species in the model at high latitudes. The model shows how the distortion of the vortex in March led to relatively high columns of ClONO2 in vortex air over southern Europe. The model also reproduces the observed gradient in ClONO2 within the vortex, and experiments show that these gradients are due, at least in part, to the availability of sunlight. This variability of ClONO2, and therefore active chlorine (ClOχ), implies that these tracers do not correlate well with potential vorticity. This places limitations on extrapolating localized measurements of anything but the longest lived chemical tracers to the whole of the polar vortex using potential vorticity, or indeed a long-lived tracer, as part of a coordinate system.


Journal of Geophysical Research | 2015

Stratospheric sulfur and its implications for radiative forcing simulated by the chemistry climate model EMAC

C. Brühl; J. Lelieveld; H. Tost; M. Höpfner; N. Glatthor

Multiyear simulations with the atmospheric chemistry general circulation model EMAC with a microphysical modal aerosol module at high vertical resolution demonstrate that the sulfur gases COS and SO2, the latter from low-latitude and midlatitude volcanic eruptions, predominantly control the formation of stratospheric aerosol. Marine dimethyl sulfide (DMS) and other SO2 sources, including strong anthropogenic emissions in China, are found to play a minor role except in the lowermost stratosphere. Estimates of volcanic SO2 emissions are based on satellite observations using Total Ozone Mapping Spectrometer and Ozone Monitoring Instrument for total injected mass and Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) on Envisat or Stratospheric Aerosol and Gases Experiment for the spatial distribution. The 10 year SO2 and COS data set of MIPAS is also used for model evaluation. The calculated radiative forcing of stratospheric background aerosol including sulfate from COS and small contributions by DMS oxidation, and organic aerosol from biomass burning, is about 0.07W/m2. For stratospheric sulfate aerosol from medium and small volcanic eruptions between 2005 and 2011 a global radiative forcing up to 0.2W/m2 is calculated, moderating climate warming, while for the major Pinatubo eruption the simulated forcing reaches 5W/m2, leading to temporary climate cooling. The Pinatubo simulation demonstrates the importance of radiative feedback on dynamics, e.g., enhanced tropical upwelling, for large volcanic eruptions.


Journal of Geophysical Research | 1995

Spatial and temporal variability of ClONO2, HNO3, and O3 in the Arctic winter of 1992/1993 as obtained by airborne infrared emission spectroscopy

C. E. Blom; H. Fischer; N. Glatthor; T. Gulde; M. Höpfner; C. Piesch

In the winter of 1992/1993 the airborne Michelson interferometer for passive atmospheric sounding (MIPAS-FT) was operated on board a German research aircraft (Transall C-160) to record infrared emission spectra of the atmosphere inside and outside the Arctic vortex. Measurements were made during four campaigns between December 4, 1992, and March 29, 1993, in the European Arctic as well as over central and southern Europe (82°N–37.5°N). We present the retrieved zenith column amounts of the stratospheric trace gases ClONO2, HNO3, and O3 of this period. Inside the polar vortex, the column amounts of ClONO2 and HNO3 were considerably enhanced already in early December, up to 3.1×1015 cm−2 and 2.7×1016 cm−2, respectively. Around the end of January, low ClONO2 (1×1015 cm−2) and high HNO3 column amounts (up to 3.7×1016 cm−2) were observed inside the vortex, whereas a highly variable “collar” of ClONO2 had developed at the vortex edge. During March, after temperatures had been above the threshold for polar stratospheric clouds (PSCs) for several weeks, we measured lower HNO3 (below 2.5×1016 cm−2) and very high ClONO2 column amounts (up to 6×1015 cm−2) inside the vortex. Thus a major part of the reactive chlorine had been converted into ClONO2, and the potential for rapid ozone depletion was reduced markedly in the region observed. On March 10, when the polar vortex extended southward to the Mediterranean, ClONO2 column amounts as high as 4.6×1015 cm−2 were observed at 40°N. At the end of March, considerable amounts of ClONO2 (up to 3.4×1015 cm−2) were measured also far outside the vortex.


Applied Optics | 2000

Optimized spectral microwindows for data analysis of the Michelson Interferometer for Passive Atmospheric Sounding on the Environmental Satellite

Georg Echle; Thomas von Clarmann; A. Dudhia; J.-M. Flaud; B. Funke; N. Glatthor; Brian J. Kerridge; M. López-Puertas; Francisco Javier Martin-Torres; Gabriele P. Stiller

For data analysis of the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) atmospheric limb emission spectroscopic experiment on Environmental Satellite microwindows, i.e., small spectral regions for data analysis, have been defined and optimized. A novel optimization scheme has been developed for this purpose that adjusts microwindow boundaries such that the total retrieval error with respect to measurement noise, parameter uncertainties, and systematic errors is minimized. Dedicated databases that contain optimized microwindows for retrieval of vertical profiles of pressure and temperature, H2O, O3, HNO3, CH4, N2O, and NO2 have been generated. Furthermore, a tool for optimal selection of subsets of predefined microwindows for specific retrieval situations has been provided. This tool can be used further for estimating total retrieval errors for a selected microwindow subset. It has been shown by use of this tool that an altitude-dependent definition of microwindows is superior to an altitude-independent definition. For computational efficiency a dedicated microwindow-related list of spectral lines has been defined that contains only those spectral lines that are of relevance for MIPAS limb sounding observations.


Journal of the Atmospheric Sciences | 2005

Three-dimensional model study of the Antarctic ozone hole in 2002 and comparison with 2000

W. Feng; M. P. Chipperfield; Howard K. Roscoe; John J. Remedios; Alison Waterfall; G. P. Stiller; N. Glatthor; M. Höpfner; D.-Y. Wang

Abstract An offline 3D chemical transport model (CTM) has been used to study the evolution of the Antarctic ozone hole during the sudden warming event of 2002 and to compare it with similar simulations for 2000. The CTM has a detailed stratospheric chemistry scheme and was forced by ECMWF and Met Office analyses. Both sets of meteorological analyses permit the CTM to produce a good simulation of the evolution of the 2002 vortex and its breakup, based on O3 comparisons with Total Ozone Mapping Spectrometer (TOMS) column data, sonde data, and first results from the Environmental Satellite–Michelson Interferometer for Passive Atmospheric Sounding (ENVISAT–MIPAS) instrument. The ozone chemical loss rates in the polar lower stratosphere in September 2002 were generally less than in 2000, because of the smaller average active chlorine, although around the time of the warming, the largest vortex chemical loss rates were similar to those in 2000 (i.e., −2.6 DU day−1 between 12 and 26 km). However, the disturbed v...


Asia-Pacific Symposium on Remote Sensing of the Atmosphere, Environment, and Space | 1998

Karlsruhe optimized and precise radiative transfer algorithm. Part I: requirements, justification, and model error estimation

Gabriele P. Stiller; Michael Hoepfner; Martin Kuntz; Thomas von Clarmann; Georg Echle; Herbert Fischer; B. Funke; N. Glatthor; F. Hase; Holger Kemnitzer; Sabine Zorn

We present the Karlsruhe Optimized and Precise Radiative transfer Algorithm (KOPRA) which has been specifically developed for data analysis of the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) going to be launched on ESAs polar-orbiting Environmental Satellite 1 (ENVISAT-1) in 1999. KOPRA has been designed to account for the particular instrument requirements of MIPAS and the observation scenarii during the ENVISAT mission, in particular with respect to the viewing direction and the altitude coverage of the atmosphere. The conceptual details of KOPRA, which reflect the requirements set up by the instrument design details, the observation scenarii, and the link to a retrieval concept with high flexibility, are presented. The forward model error due to discarding individual physical processes and properties of the atmosphere as well as an over-all error budget with respect to these parameters is assessed in order to demonstrate the improvements of retrieval accuracy expected by usage of KOPRA.

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M. Höpfner

Karlsruhe Institute of Technology

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G. P. Stiller

Karlsruhe Institute of Technology

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S. Kellmann

Karlsruhe Institute of Technology

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U. Grabowski

Karlsruhe Institute of Technology

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B. Funke

Karlsruhe Institute of Technology

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T. von Clarmann

Karlsruhe Institute of Technology

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A. Linden

Karlsruhe Institute of Technology

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M. López-Puertas

Spanish National Research Council

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M. Kiefer

Karlsruhe Institute of Technology

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