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Featured researches published by G. Günther.


Journal of Geophysical Research | 2010

Impact of the vertical velocity scheme on modeling transport in the tropical tropopause layer

Felix Ploeger; P. Konopka; G. Günther; J.-U. Grooß; Ralph Müller

[1] To assess the impact of the vertical velocity scheme on modeling transport in the tropical tropopause layer (TTL), 3 month backward trajectories are initialized in the TTL for boreal winter and summer 2002. The calculations are done in either a kinematic scenario with pressure tendency as the vertical velocity or in a diabatic scenario with cross-isentropic velocity deduced from various diabatic heating rates due to radiation (clear sky, all sky) and latent, diffusive and turbulent heating. This work provides a guideline for assessing the sensitivity of trajectory and chemical transport model (CTM) results on the choice of the vertical velocity scheme. We find that many transport characteristics, such as time scales, pathways and dispersion, crucially depend on the vertical velocity scheme. The strongest tropical upwelling results from the operational European Centre for Medium-Range Weather Forecasts kinematic scenario with the time scale for ascending from 340 to 400 K of 1 month. For the ERA-Interim kinematic and total diabatic scenarios, this time scale is about 2 months, and for the all-sky scenario it is as long as 2.5 months. In a diabatic scenario, the whole TTL exhibits mean upward motion, whereas in a kinematic scenario, regions of subsidence occur in the upper TTL. However, some transport characteristics robustly emerge from the different scenarios, such as an enhancement of residence times between 350 and 380 K and a strong impact of meridional in-mixing from the extratropics on the composition of the TTL. Moreover, an increase of meridionally transported air from the summer hemisphere into the TTL (maximum for boreal summer) is found as an invariant feature among all the scenarios.


Geophysical Research Letters | 2010

What causes the irregular cycle of the atmospheric tape recorder signal in HCN

R. Pommrich; Ralph Müller; J.-U. Grooß; G. Günther; P. Konopka; Martin Riese; A. Heil; Martin G. Schultz; Hugh C. Pumphrey; Kaley A. Walker

Received 27 May 2010; accepted 8 July 2010; published 20 August 2010. [1] Variations in the mixing ratio of long‐lived trace gases entering the stratosphere in the tropics are carried upward with the rising air with the signal being observable throughout the tropical lower stratosphere. This phenomenon, referred to as “atmospheric tape recorder” has previously been observed for water vapor, CO2 ,a nd CO which exhibit an annual cycle. Recently, based on Microwave Limb Sounder (MLS) and the Atmospheric Chemistry Experiment Fourier Transform Spectrometer (ACE‐ FTS) satellite measurements, the tape recorder signal has been observed for hydrogen cyanide (HCN) but with an approximately two‐year period. Here we report on a model simulation of the HCN tape recorder for the time period 2002–2008 using the Chemical Lagrangian Model of the Stratosphere (CLaMS). The model can reproduce the observed pattern of the HCN tape recorder signal if time‐resolved emissions from fires in Indonesia are used as lower boundary condition. This finding indicates that inter‐annual variations in biomass burning in Indonesia, which are strongly influenced by El Nino events, control the HCN tape recorder signal. A longer time series of tropical HCN data will probably exhibit an irregular cycle rather than a regular biannual cycle. Citation: Pommrich, R., R. Muller, J.-U. Groos, G. Gunther, P. Konopka, M. Riese, A. Heil, M. Schultz, H.-C. Pumphrey, and K. A. Walker (2010), What causes the irregular cycle of the atmospheric tape recorder signal in HCN?, Geophys. Res. Lett., 37, L16805, doi:10.1029/ 2010GL044056.


Journal of the Atmospheric Sciences | 2003

A generalized form of lait's modified potential vorticity

Rolf Müller; G. Günther

Abstract Ertels potential vorticity P is in widespread use as a diagnostic of dynamical processes in the stratosphere. For a variety of applications, however, the exponential increase of P with altitude is problematic. For this reason, Lait proposed a modified potential vorticity ΠL, where a physically meaningful scaling is introduced that removes much of the altitude dependence of P. Here a generalized form of ΠL is proposed by introducing an additional degree of freedom in the scaling. This generalized modified potential vorticity Πg possesses the same conservation properties as ΠL itself and as the classic potential vorticity P but can be adjusted more closely to the specific situation under investigation. Comparison, over a large altitude range in the stratosphere, of fields of Πg with dynamical measures of the polar vortex edge and with observations of the long-lived trace gas N2O shows that Πg constitutes a more intuitively interpretable quantity than ΠL.


Journal of Atmospheric Chemistry | 2003

Intercomparison of Stratospheric Chemistry Models under Polar Vortex Conditions

Martina Krämer; R. I. Müller; Heinrich Bovensmann; J. P. Burrows; J. Brinkmann; E. P. Röth; J.-U. Grooß; R. O. Müller; T. H. Woyke; R. Ruhnke; G. Günther; J. Hendricks; E. Lippert; Kenneth S. Carslaw; T. Peter; A. Zieger; C. Brühl; Benedikt Steil; R. Lehmann; Daniel S. McKenna

Several stratospheric chemistry modules from box, 2-D or 3-D models, have been intercompared. The intercomparison was focused on the ozone loss and associated reactive species under the conditions found in the cold, wintertime Arctic and Antarctic vortices. Comparisons of both gas phase and heterogeneous chemistry modules show excellent agreement between the models under constrained conditions for photolysis and the microphysics of polar stratospheric clouds. While the mean integral ozone loss ranges from 4–80% for different 30–50 days long air parcel trajectories, the mean scatter of model results around these values is only about ±1.5%. In a case study, where the models employed their standard photolysis and microphysical schemes, the variation around the mean percentage ozone loss increases to about ±7%. This increased scatter of model results is mainly due to the different treatment of the PSC microphysics and heterogeneous chemistry in the models, whereby the most unrealistic assumptions about PSC processes consequently lead to the least representative ozone chemistry. Furthermore, for this case study the model results for the ozone mixing ratios at different altitudes were compared with a measured ozone profile to investigate the extent to which models reproduce the stratospheric ozone losses. It was found that mainly in the height range of strong ozone depletion all models underestimate the ozone loss by about a factor of two. This finding corroborates earlier studies and implies a general deficiency in our understanding of the stratospheric ozone loss chemistry rather than a specific problem related to a particular model simulation.


Advances in Space Research | 1999

Simulation of middle atmosphere winds and comparison with mesopause region wind measurements

Martin Lange; R. Schminder; Ch. Jacobi; F. Baier; G. Günther

Abstract Wind field simulations with a simple mechanistic circulation model are performed for solstice conditions. The mean zonal wind as well as the temperature field are in good agreement with realistic conditions, and agree with climatologies from literature. The semidiurnal tide at 52°N is compared with the long term data set from Collm and Juliusruh, Germany. For several cases it is shown that measurements are well represented by the simulations.


Atmospheric Chemistry and Physics | 2017

Sensitivities of modelled water vapour in the lower stratosphere: temperature uncertainty, effects of horizontal transport and small-scale mixing

Liubov Poshyvailo; Rolf Müller; Paul Konopka; G. Günther; Martin Riese; Felix Ploeger

Water vapour (H2O) in the upper troposphere and lower stratosphere (UTLS) has a significant role for global radiation. A realistic representation of H2O is therefore critical for accurate climate model predictions of future climate change. In this paper we investigate the effects of current uncertainties in tropopause temperature, horizontal transport and small-scale mixing on simulated H2O in the lower stratosphere (LS). To assess the sensitivities of simulated H2O, we use the Chemical Lagrangian Model of the Stratosphere (CLaMS). First, we examine CLaMS, which is driven by two reanalyses, from the European Centre of Medium-Range Weather Forecasts (ECMWF) ERA-Interim and the Japanese 55-year Reanalysis (JRA-55), to investigate the robustness with respect to the meteorological dataset. Second, we carry out CLaMS simulations with transport barriers along latitude circles (at the Equator, 15 and 35 N/S) to assess the effects of horizontal transport. Third, we vary the strength of parametrized small-scale mixing in CLaMS. Our results show significant differences (about 0.5 ppmv) in simulated stratospheric H2O due to uncertainties in the tropical tropopause temperatures between the two reanalysis datasets, JRA-55 and ERA-Interim. The JRA-55 based simulation is significantly moister when compared to ERAInterim, due to a warmer tropical tropopause (approximately 2 K). The transport barrier experiments demonstrate that the Northern Hemisphere (NH) subtropics have a strong moistening effect on global stratospheric H2O. The comparison of tropical entry H2O from the sensitivity 15 N/S barrier simulation and the reference case shows differences of up to around 1 ppmv. Interhemispheric exchange shows only a very weak effect on stratospheric H2O. Small-scale mixing mainly increases troposphere–stratosphere exchange, causing an enhancement of stratospheric H2O, particularly along the subtropical jets in the summer hemisphere and in the NH monsoon regions. In particular, the Asian and American monsoon systems during a boreal summer appear to be regions especially sensitive to changes in small-scale mixing, which appears crucial for controlling the moisture anomalies in the monsoon UTLS. For the sensitivity simulation with varied mixing strength, differences in tropical entry H2O between the weak and strong mixing cases amount to about 1 ppmv, with small-scale mixing enhancing H2O in the LS. The sensitivity studies presented here provide new insights into the leading processes that control stratospheric H2O, which are important for assessing and improving climate model projections.


Atmospheric Chemistry and Physics | 2018

Lagrangian simulations of the transport of young air masses to the top of the Asian monsoon anticyclone and into the tropical pipe

Bärbel Vogel; Rolf Müller; G. Günther; Reinhold Spang; Sreeharsha Hanumanthu; Dan Li; Martin Riese; Gabriele P. Stiller

We have performed backward trajectory calculations and simulations with the three-dimensional Chemical Lagrangian Model of the Stratosphere (CLaMS) for two succeeding monsoon seasons using artificial tracers of air mass origin. With these tracers we trace back the origin of young air masses (age < 6 months) at the top of the Asian monsoon anticyclone and of air masses within the tropical pipe (6 months< age< 18 months) during summer 2008. The occurrence of young air masses (< 6 months) at the top of the Asian monsoon anticyclone up to ∼ 460 K is in agreement with satellite measurements of chlorodifluoromethane (HCFC-22) by the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) instrument. HCFC-22 can be considered as a regional tracer for continental eastern Asia and the Middle East as it is mainly emitted in this region. Our findings show that the transport of air masses from boundary layer sources in the region of the Asian monsoon into the tropical pipe occurs in three distinct steps. First, very fast uplift in “a convective range” transports air masses up to 360 K potential temperature within a few days. Second, air masses are uplifted from about 360 K up to 460 K within “an upward spiralling range” within a few months. The largescale upward spiral extends from northern Africa to the western Pacific. The air masses are transported upwards by diabatic heating with a rate of up to 1–1.5 K per day, implying strong vertical transport above the Asian monsoon anticyclone. Third, transport of air masses occurs within the tropical pipe up to 550 K associated with the large-scale Brewer– Dobson circulation within ∼ 1 year. In the upward spiralling range, air masses are uplifted by diabatic heating across the (lapse rate) tropopause, which does not act as a transport barrier, in contrast to the extratropical tropopause. Further, in the upward spiralling range air masses from inside the Asian monsoon anticyclone are mixed with air masses convectively uplifted outside the core of the Asian monsoon anticyclone in the tropical adjacent regions. Moreover, the vertical transport of air masses from the Asian monsoon anticyclone into the tropical pipe is weak in terms of transported air masses compared to the transport from the monsoon anticyclone into the northern extratropical lower stratosphere. Air masses from the Asian monsoon anticyclone (India/China) contribute a minor fraction to the composition of air within the tropical pipe at 550 K (6 %), and the major fractions are from Southeast Asia (16 %) and the tropical Pacific (15 %).


Journal of Geophysical Research | 2002

A new Chemical Lagrangian Model of the Stratosphere (CLaMS) 1. Formulation of advection and mixing

Daniel S. McKenna; Paul Konopka; J.-U. Grooß; G. Günther; Rolf Müller; Reinhold Spang; D. Offermann; Yvan J. Orsolini


Journal of Geophysical Research | 2002

A new Chemical Lagrangian Model of the Stratosphere (CLaMS) 2. Formulation of chemistry scheme and initialization

Daniel S. McKenna; J.-U. Grooß; G. Günther; Paul Konopka; Rolf Müller; G. D. Carver; Yasuhiro Sasano


Atmospheric Chemistry and Physics | 2009

Annual cycle of ozone at and above the tropical tropopause: observations versus simulations with the Chemical Lagrangian Model of the Stratosphere (CLaMS)

P. Konopka; J.-U. Grooß; G. Günther; Felix Ploeger; R. Pommrich; Ralph Müller; Nathaniel J. Livesey

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J.-U. Grooß

Forschungszentrum Jülich

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Martin Riese

Forschungszentrum Jülich

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P. Konopka

Forschungszentrum Jülich

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Bärbel Vogel

Forschungszentrum Jülich

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Paul Konopka

Forschungszentrum Jülich

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Daniel S. McKenna

National Center for Atmospheric Research

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C. Schiller

Forschungszentrum Jülich

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F. Stroh

Forschungszentrum Jülich

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