scholarly journals Contribution of mixing to upward transport across the tropical tropopause layer (TTL)

2007 ◽  
Vol 7 (12) ◽  
pp. 3285-3308 ◽  
Author(s):  
P. Konopka ◽  
G. Günther ◽  
R. Müller ◽  
F. H. S. dos Santos ◽  
C. Schiller ◽  
...  
Keyword(s):  
Large Scale ◽  
Potential Temperature ◽  
Vertical Mixing ◽  
Chemical Species ◽  
Convective Transport ◽  
Vertical Shear ◽  
Lagrangian Model ◽  
Tropical Tropopause ◽  
Upward Transport ◽  
Meteorological Analysis

Abstract. During the second part of the TROCCINOX campaign that took place in Brazil in early 2005, chemical species were measured on-board the high-altitude research aircraft Geophysica (ozone, water vapor, NO, NOy, CH4 and CO) in the altitude range up to 20 km (or up to 450 K potential temperature), i.e. spanning the entire TTL region roughly extending between 350 and 420 K. Here, analysis of transport across the TTL is performed using a new version of the Chemical Lagrangian Model of the Stratosphere (CLaMS). In this new version, the stratospheric model has been extended to the earth surface. Above the tropopause, the isentropic and cross-isentropic advection in CLaMS is driven by meteorological analysis winds and heating/cooling rates derived from a radiation calculation. Below the tropopause, the model smoothly transforms from the isentropic to the hybrid-pressure coordinate and, in this way, takes into account the effect of large-scale convective transport as implemented in the vertical wind of the meteorological analysis. As in previous CLaMS simulations, the irreversible transport, i.e. mixing, is controlled by the local horizontal strain and vertical shear rates. Stratospheric and tropospheric signatures in the TTL can be seen both in the observations and in the model. The composition of air above ≈350 K is mainly controlled by mixing on a time scale of weeks or even months. Based on CLaMS transport studies where mixing can be completely switched off, we deduce that vertical mixing, mainly driven by the vertical shear in the tropical flanks of the subtropical jets and, to some extent, in the the outflow regions of the large-scale convection, offers an explanation for the upward transport of trace species from the main convective outflow at around 350 K up to the tropical tropopause around 380 K.

scholarly journals Contribution of mixing to the upward transport across the TTL

2006 ◽  
Vol 6 (6) ◽  
pp. 12217-12266 ◽  
Author(s):  
P. Konopka ◽  
G. Günther ◽  
R. Müller ◽  
F. H. S. dos Santos ◽  
C. Schiller ◽  
...  
Keyword(s):  
Large Scale ◽  
Potential Temperature ◽  
Vertical Mixing ◽  
Chemical Species ◽  
Convective Transport ◽  
Vertical Shear ◽  
Lagrangian Model ◽  
Tropical Tropopause ◽  
Upward Transport ◽  
Subtropical Jets

Abstract. During the second part of the TROCCINOX campaign that took place in Brazil in early 2005, chemical species were measured on-board of the high altitude research aircraft Geophysica (ozone, water vapor, NO, NOy, CH4 and CO) in the altitude range up to 20 km (or up to 450 K potential temperature), i.e. spanning the TTL region roughly extending between 350 and 420 K. Analysis of transport across TTL is performed using a new version of the Chemical Lagrangian Model of the Stratosphere (CLaMS). In this new version, the stratospheric model has been extended to the earth surface. Above the tropopause, the isentropic and cross-isentropic advection in CLaMS is driven by ECMWF winds and heating/cooling rates derived from a radiation calculation. Below the tropopause the model smoothly transforms from the isentropic to hybrid-pressure coordinate and, in this way, takes into account the effect of large-scale convective transport as implemented in the ECMWF vertical wind. As with other CLaMS simulations, the irreversible transport, i.e. mixing, is controlled by the local horizontal strain and vertical shear rates. Stratospheric and tropospheric signatures in the TTL can be seen both in the observation and in the model. The composition of air above ≈350 K is mainly controlled by mixing on a time scale of weeks or even months. Based on CLaMS transport studies where mixing can be completely switched off, we deduce that vertical mixing, mainly driven by the vertical shear in the outflow regions of the large-scale convection and in the vicinity of the subtropical jets, is necessary to understand the upward transport of the tropospheric air from the main convective outflow around 350 K up to the tropical tropopause around 380 K. This mechanism is most effective if the outflow of the mesoscale convective systems interacts with the subtropical jets.

scholarly journals Nitrification of the lowermost stratosphere during the exceptionally cold Arctic winter 2015–2016

2019 ◽  
Vol 19 (21) ◽  
pp. 13681-13699 ◽  
Author(s):  
Marleen Braun ◽  
Jens-Uwe Grooß ◽  
Wolfgang Woiwode ◽  
Sören Johansson ◽  
Michael Höpfner ◽  
...  
Keyword(s):  
Nitric Acid ◽  
Cross Sections ◽  
Large Scale ◽  
Potential Temperature ◽  
Lagrangian Model ◽  
The Arctic ◽  
Small Scale ◽  
Mixing Ratios ◽  
Fine Structures ◽  
The Impact

Abstract. The Arctic winter 2015–2016 was characterized by exceptionally low stratospheric temperatures, favouring the formation of polar stratospheric clouds (PSCs) from mid-December until the end of February down to low stratospheric altitudes. Observations by GLORIA (Gimballed Limb Observer for Radiance Imaging of the Atmosphere) on HALO (High Altitude and LOng range research aircraft) during the PGS (POLSTRACC–GW-LCYCLE II–SALSA) campaign from December 2015 to March 2016 allow the investigation of the influence of denitrification on the lowermost stratosphere (LMS) with a high spatial resolution. Two-dimensional vertical cross sections of nitric acid (HNO3) along the flight track and tracer–tracer correlations derived from the GLORIA observations document detailed pictures of wide-spread nitrification of the Arctic LMS during the course of an entire winter. GLORIA observations show large-scale structures and local fine structures with enhanced absolute HNO3 volume mixing ratios reaching up to 11 ppbv at altitudes of 13 km in January and nitrified filaments persisting until the middle of March. Narrow coherent structures tilted with altitude of enhanced HNO3, observed in mid-January, are interpreted as regions recently nitrified by sublimating HNO3-containing particles. Overall, extensive nitrification of the LMS between 5.0 and 7.0 ppbv at potential temperature levels between 350 and 380 K is estimated. The GLORIA observations are compared with CLaMS (Chemical Lagrangian Model of the Stratosphere) simulations. The fundamental structures observed by GLORIA are well reproduced, but differences in the fine structures are diagnosed. Further, CLaMS predominantly underestimates the spatial extent of HNO3 maxima derived from the GLORIA observations as well as the overall nitrification of the LMS. Sensitivity simulations with CLaMS including (i) enhanced sedimentation rates in case of ice supersaturation (to resemble ice nucleation on nitric acid trihydrate (NAT)), (ii) a global temperature offset, (iii) modified growth rates (to resemble aspherical particles with larger surfaces) and (iv) temperature fluctuations (to resemble the impact of small-scale mountain waves) slightly improved the agreement with the GLORIA observations of individual flights. However, no parameter could be isolated which resulted in a general improvement for all flights. Still, the sensitivity simulations suggest that details of particle microphysics play a significant role for simulated LMS nitrification in January, while air subsidence, transport and mixing become increasingly important for the simulated HNO3 distributions towards the end of the winter.

scholarly journals Nitrification of the lowermost stratosphere during the exceptionally cold Arctic winter 2015/16

2019 ◽  
Author(s):  
Marleen Braun ◽  
Jens-Uwe Grooß ◽  
Wolfgang Woiwode ◽  
Sören Johansson ◽  
Michael Höpfner ◽  
...  
Keyword(s):  
Cross Sections ◽  
Large Scale ◽  
Potential Temperature ◽  
Lagrangian Model ◽  
The Arctic ◽  
Small Scale ◽  
Mountain Waves ◽  
Mixing Ratios ◽  
Fine Structures ◽  
The Impact

Abstract. The Arctic winter 2015/16 was characterized by exceptionally cold stratospheric temperatures, favouring the formation of polar stratospheric clouds (PSCs) from mid-December until the end of February down to low stratospheric altitudes. Observations by GLORIA (Gimballed Limb Observer for Radiance Imaging of the Atmosphere) on HALO (High Altitude and LOng range research aircraft) during the PGS (POLSTRACC/GW-LCYLCE II/SALSA) campaign from December 2015 to March 2016 allow an investigation of the influence of denitrification on the lowermost stratosphere (LMS) with a high spatial resolution. For the first time vertical cross-sections of nitric acid (HNO3) along the flight track and tracer-tracer correlations derived from the GLORIA observations document detailed pictures of wide-spread nitrification of the Arctic LMS during the course of an entire winter. GLORIA observations show large-scale structures and local fine structures with strongly enhanced absolute HNO3 volume mixing ratios reaching up to 11 ppbv at altitudes of 11 km in January and nitrified filaments persisting until the middle of March. Narrow streaks of enhanced HNO3, observed in mid-January, are interpreted as regions recently nitrified by sublimating HNO3-containing particles. Overall, a nitrification of the LMS between 5.0 ppbv and 7.0 ppbv at potential temperature levels between 350 and 380 K is estimated. This extent of nitrification has never been observed before in the Arctic lowermost stratosphere. The GLORIA observations are compared with CLaMS (Chemical Lagrangian Model of the Stratosphere) simulations. The fundamental structures observed by GLORIA are well reproduced, but differences in the fine structures are diagnosed. Further, CLaMS predominantly underestimates the spatial extent of maximum HNO3 mixing ratios derived from the GLORIA observations as well as the enhancement at lower altitudes. Sensitivity simulations with CLaMS including (i) enhanced sedimentation rates in case of ice supersaturation (to resemble ice nucleation on NAT), (ii) a global temperature offset, (iii) modified growth rates (to resemble aspherical particles with larger surfaces) and (iv) temperature fluctuations (to resemble the impact of small-scale mountain waves) mostly improve the agreement with the GLORIA observations. The sensitivity simulations suggest that details of particle microphysics play a significant role for simulated LMS nitrification in January, while air subsidence, transport and mixing become increasingly important towards the end of the winter.

scholarly journals Characterization of a boreal convective boundary layer and its impact on atmospheric chemistry during HUMPPA-COPEC-2010

2012 ◽  
Vol 12 (19) ◽  
pp. 9335-9353 ◽  
Author(s):  
H. G. Ouwersloot ◽  
J. Vilà-Guerau de Arellano ◽  
A. C. Nölscher ◽  
M. C. Krol ◽  
L. N. Ganzeveld ◽  
...  
Keyword(s):  
Boundary Layer ◽  
Atmospheric Chemistry ◽  
Convective Boundary Layer ◽  
Large Scale ◽  
Spatial Scales ◽  
Potential Temperature ◽  
Chemical Species ◽  
Convective Boundary ◽  
The Impact

Abstract. We studied the atmospheric boundary layer (ABL) dynamics and the impact on atmospheric chemistry during the HUMPPA-COPEC-2010 campaign. We used vertical profiles of potential temperature and specific moisture, obtained from 132 radio soundings, to determine the main boundary layer characteristics during the campaign. We propose a classification according to several main ABL prototypes. Further, we performed a case study of a single day, focusing on the convective boundary layer, to analyse the influence of the dynamics on the chemical evolution of the ABL. We used a mixed layer model, initialized and constrained by observations. In particular, we investigated the role of large scale atmospheric dynamics (subsidence and advection) on the ABL development and the evolution of chemical species concentrations. We find that, if the large scale forcings are taken into account, the ABL dynamics are represented satisfactorily. Subsequently, we studied the impact of mixing with a residual layer aloft during the morning transition on atmospheric chemistry. The time evolution of NOx and O3 concentrations, including morning peaks, can be explained and accurately simulated by incorporating the transition of the ABL dynamics from night to day. We demonstrate the importance of the ABL height evolution for the representation of atmospheric chemistry. Our findings underscore the need to couple the dynamics and chemistry at different spatial scales (from turbulence to mesoscale) in chemistry-transport models and in the interpretation of observational data.

scholarly journals Cloud system resolving model study of the roles of deep convection for photo-chemistry in the TOGA COARE/CEPEX region

2008 ◽  
Vol 8 (10) ◽  
pp. 2741-2757 ◽  
Author(s):  
M. Salzmann ◽  
M. G. Lawrence ◽  
V. T. J. Phillips ◽  
L. J. Donner
Keyword(s):  
Large Scale ◽  
Marine Boundary Layer ◽  
Deep Convection ◽  
Trace Gases ◽  
Convective Transport ◽  
Cloud System ◽  
Limited Area ◽  
Toga Coare ◽  
Upward Transport ◽  
Photo Chemistry

Abstract. A cloud system resolving model including photo-chemistry (CSRMC) has been developed based on a prototype version of the Weather Research and Forecasting (WRF) model and is used to study influences of deep convection on chemistry in the TOGA COARE/CEPEX region. Lateral boundary conditions for trace gases are prescribed from global chemistry-transport simulations, and the vertical advection of trace gases by large scale dynamics, which is not reproduced in a limited area cloud system resolving model, is taken into account. The influences of deep convective transport and of lightning on NOx, O3, and HOx(=HO2+OH), in the vicinity of the deep convective systems are investigated in a 7-day 3-D 248×248 km2 horizontal domain simulation and several 2-D sensitivity runs with a 500 km horizontal domain. Mid-tropospheric entrainment is more important on average for the upward transport of O3 in the 3-D run than in the 2-D runs, but at the same time undiluted O3-poor air from the marine boundary layer reaches the upper troposphere more frequently in the 3-D run than in the 2-D runs, indicating the presence of undiluted convective cores. In all runs, in situ lightning is found to have only minor impacts on the local O3 budget. Near zero O3 volume mixing ratios due to the reaction with lightning-produced NO are only simulated in a 2-D sensitivity run with an extremely high number of NO molecules per flash, which is outside the range of current estimates. The fraction of NOx chemically lost within the domain varies between 20 and 24% in the 2-D runs, but is negligible in the 3-D run, in agreement with a lower average NOx concentration in the 3-D run despite a greater number of flashes. Stratosphere to troposphere transport of O3 is simulated to occur episodically in thin filaments in the 2-D runs, but on average net upward transport of O3 from below ~16 km is simulated in association with mean large scale ascent in the region. Ozone profiles in the TOGA COARE/CEPEX region are suggested to be strongly influenced by the intra-seasonal (Madden-Julian) oscillation.

scholarly journals Mixing and Chemical Ozone Loss during and after the Antarctic Polar Vortex Major Warming in September 2002

2005 ◽  
Vol 62 (3) ◽  
pp. 848-859 ◽  
Author(s):  
Paul Konopka ◽  
Jens-Uwe Grooß ◽  
Karl W. Hoppel ◽  
Hildegard-Maria Steinhorst ◽  
Rolf Müller
Keyword(s):  
Potential Temperature ◽  
Polar Vortex ◽  
Vertical Shear ◽  
Lagrangian Model ◽  
Ozone Loss ◽  
Time Period ◽  
The Difference ◽  
Antarctic Polar Vortex ◽  
The Antarctic ◽  
Vortex Split

Abstract The 3D version of the Chemical Lagrangian Model of the Stratosphere (CLAMS) is used to study the transport of CH4 and O3 in the Antarctic stratosphere between 1 September and 30 November 2002, that is, over the time period when unprecedented major stratospheric warming in late September split the polar vortex into two parts. The isentropic and cross-isentropic velocities in CLAMS are derived from ECMWF winds and heating/cooling rates calculated with a radiation module. The irreversible part of transport, that is, mixing, is driven by the local horizontal strain and vertical shear rates with mixing parameters deduced from in situ observations. The CH4 distribution after the vortex split shows a completely different behavior above and below 600 K. Above this potential temperature level, until the beginning of November, a significant part of vortex air is transported into the midlatitudes up to 40°S. The lifetime of the vortex remnants formed after the vortex split decreases with the altitude with values of about 3 and 6 weeks at 900 and 700 K, respectively. Despite this enormous dynamical disturbance of the vortex, the intact part between 400 and 600 K that “survived” the major warming was strongly isolated from the extravortex air until the end of November. According to CLAMS simulations, the air masses within this part of the vortex did not experience any significant dilution with the midlatitude air. By transporting ozone in CLAMS as a passive tracer, the chemical ozone loss was estimated from the difference between the observed [Polar Ozone and Aerosol Measurement III (POAM III) and Halogen Occultation Experiment (HALOE)] and simulated ozone profiles. Starting from 1 September, up to 2.0 ppmv O3 around 480 K and about 70 Dobson units between 450 and 550 K were destroyed until the vortex was split. After the major warming, no additional ozone loss can be derived, but in the intact vortex part between 450 and 550 K, the accumulated ozone loss was “frozen in” until the end of November.

scholarly journals Contribution of very short-lived substances to stratospheric bromine loading: uncertainties and constraints

2012 ◽  
Vol 12 (11) ◽  
pp. 30283-30326
Author(s):  
J. Aschmann ◽  
B.-M. Sinnhuber
Keyword(s):  
Large Scale ◽  
Transport Model ◽  
Gas Injection ◽  
Critical Factor ◽  
Significant Loss ◽  
Convective Transport ◽  
Heterogeneous Reactions ◽  
Minor Role ◽  
Tropical Tropopause ◽  
Ice Particles

Abstract. Very short-lived substances (VSLS) still represent a major factor of uncertainty in the quantification of stratospheric bromine loading. One of the major obstacles for short-lived source gases in contributing to the stratosphere is generally thought to be loss of inorganic bromine (Bry) in the tropical tropopause layer (TTL) due to dehydration. We use sensitivity calculations with a~three-dimensional chemistry transport model comprising a consistent parametrization of convective transport and a comprehensive chemistry scheme to investigate the associated processes. The model considers the two most important bromine VSLS, bromoform (CHBr3) and dibromomethane (CH2Br2). The organic bromine source gases as well as the resulting profile of inorganic bromine in the model are consistent with available observations. In contrast to its organic precursors, Bry is assumed to have a~significant sorption capacity regarding sedimenting liquid or frozen particles thus the fraction of intact source gases during their ascent through the TTL is a critical factor. We find that source gas injection is the dominant pathway into the stratosphere, about 50% of CHBr3 and 93% of CH2Br2 is able to overcome the cold point tropopause at approximately 17 km altitude, modulated by the interannual variability of the vertical transport efficiency. In fact, our sensitivity calculations indicate that the extent of source gas injection of CHBr3 is highly sensitive to the strength of convection and large-scale ascent; in contrast, modifying the photolysis or the destruction via OH yields a significantly smaller response. In principal, the same applies as well to CH2Br2, though it is considerably less responsive due to its longer lifetime. The next important aspect we identified is that the partitioning of available Bry from short-lived sources is clearly shifted away from HBr, according to our current state of knowledge the only member of the Bry family which is efficiently adsorbed on ice particles. This effect is caused by very efficient heterogeneous reactions on ice surfaces which reduce the HBr/Bry fraction below 15% at the tropical tropopause. Under these circumstances there is no significant loss of Bry due to dehydration in the model, VSLS contribute fully to stratospheric bromine. In addition, we conduct several sensitivity calculations to test the robustness of this result. If heterogeneous chemistry is ignored, the HBr/Bry fraction exceeds 50% and about 10% of bromine from VSLS is scavenged. Dehydration plays a minor role for Bry removal under the assumption that HOBr is efficiently adsorbed on ice as well since the heterogeneous reactions alter the partitioning equilibrium of Bry in favor of HOBr. In this case, up to 12% of bromine from VSLS is removed. Even in the extreme and unrealistic case that adsorbed species on ice particles are instantaneously removed the maximum loss of bromine does not exceed 25%. In conclusion, considering the average abundance of bromine short-lived source gases in convective updrafts of 6 parts per trillion by volume (pptv) we find a most likely contribution of VSLS to stratospheric bromine in the range of 4.5–6 pptv.

scholarly journals Cirrus and water vapor transport in the tropical tropopause layer: a modeling study

2012 ◽  
Vol 12 (4) ◽  
pp. 10729-10773 ◽  
Author(s):  
T. Dinh ◽  
D. R. Durran ◽  
T. Ackerman
Keyword(s):  
Water Vapor ◽  
Large Scale ◽  
Vertical Direction ◽  
Water Vapor Transport ◽  
Kelvin Wave ◽  
Tropical Tropopause Layer ◽  
Mesoscale Dynamics ◽  
Tropical Tropopause ◽  
Upward Transport ◽  
Microphysical Processes

Abstract. We carry out simulations of tropical-tropopause-layer (TTL) cirrus which are formed and forced by a large-scale equatorial Kelvin wave. We find that, even under the influence of the large-scale wave, the radiatively induced mesoscale dynamics in TTL cirrus actively contributes to transport of water vapor in the vertical direction. In a typical TTL cirrus, the heating that results from absorption of radiation by ice crystals induces a mesoscale circulation. Advection of water vapor by the radiatively induced circulation leads to upward advection of the cloudy air. Upward advection of the cloudy air is equivalent to upward transport of water vapor when the air above the cloud is drier than the cloudy air. On the other hand, ice nucleation and depositional growth, followed by sedimentation and sublimation lead to downward transport of water vapor. The net direction of transport is determined by the relative magnitudes of the upward advection of water vapor and the downward transport associated with microphysical processes.

scholarly journals Synoptic-Scale Precursors to Tropical Cyclone Rapid Intensification in the Atlantic Basin

2015 ◽  
Vol 2015 ◽  
pp. 1-16 ◽  
Author(s):  
Alexandria Grimes ◽  
Andrew E. Mercer
Keyword(s):  
Tropical Cyclone ◽  
Large Scale ◽  
Potential Temperature ◽  
Vertical Shear ◽  
Specific Humidity ◽  
Support Vector ◽  
Rapid Intensification ◽  
Synoptic Scale ◽  
Atlantic Basin ◽  
And Cluster Analysis

Forecasting rapid intensification (hereafter referred to as RI) of tropical cyclones in the Atlantic Basin is still a challenge due to a limited understanding of the meteorological processes that are necessary for predicting RI. To address this challenge, this study considered large-scale processes as RI indicators within tropical cyclone environments. The large-scale processes were identified by formulating composite map types of RI and non-RI storms using NASA MERRA data from 1979 to 2009. The composite fields were formulated by a blended RPCA and cluster analysis approach, yielding multiple map types of RI’s and non-RI’s. Additionally, statistical differences in the large-scale processes were identified by formulating permutation tests, based on the composite output, revealing variables that were statistically significantly distinct between RI and non-RI storms. These variables were used as input in two prediction schemes: logistic regression and support vector machine classification. Ultimately, the approach identified midlevel vorticity, pressure vertical velocity, 200–850 hPa vertical shear, low-level potential temperature, and specific humidity as the most significant in diagnosing RI, yielding modest skill in identifying RI storms.

scholarly journals Cirrus and water vapor transport in the tropical tropopause layer – Part 1: A specific case modeling study

2012 ◽  
Vol 12 (20) ◽  
pp. 9799-9815 ◽  
Author(s):  
T. Dinh ◽  
D. R. Durran ◽  
T. Ackerman
Keyword(s):  
Water Vapor ◽  
Large Scale ◽  
Vertical Direction ◽  
Water Vapor Transport ◽  
Mesoscale Circulation ◽  
Kelvin Wave ◽  
Tropical Tropopause Layer ◽  
Tropical Tropopause ◽  
Upward Transport ◽  
Microphysical Processes

Abstract. In a simulation of a tropical-tropopause-layer (TTL) cirrus forced by a large-scale equatorial Kelvin wave, the radiatively induced mesoscale dynamics of the cloud actively contributes to the transport of water vapor in the vertical direction. In a typical TTL cirrus, the heating that results from absorption of radiation by ice crystals induces a mesoscale circulation. Advection of water vapor by the radiatively induced circulation leads to upward advection of the cloudy air. Upward advection of the cloudy air is equivalent to upward transport of water vapor when the air above the cloud is drier than the cloudy air. On the other hand, ice nucleation and depositional growth, followed by sedimentation and sublimation lead to downward transport of water vapor. Under the conditions specific to our simulation, the upward transport of water vapor by the mesoscale circulation dominates the downward transport by microphysical processes. The net result is upward transport of water vapor, which is equivalent to hydration of the lower stratosphere. Sensitivity to model conditions and parameters will be discussed in a follow-up paper.

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