scholarly journals Estimating Brewer-Dobson circulation trends from changes in stratospheric water vapour and methane

2021 ◽  
Author(s):  
Liubov Poshyvailo-Strube ◽  
Rolf Müller ◽  
Stephan Fueglistaler ◽  
Michaela I. Hegglin ◽  
Johannes C. Laube ◽  
...  
Keyword(s):  
Water Vapour ◽  
Meridional Overturning Circulation ◽  
Lagrangian Model ◽  
Satellite Measurements ◽  
Mixing Ratios ◽  
Transit Times ◽  
Sensitivity Studies ◽  
Meridional Overturning ◽  
Gas Measurements ◽  
Stratospheric Water Vapour

Abstract. The stratospheric meridional overturning circulation, also referred to as the Brewer-Dobson circulation (BDC), controls the composition of the stratosphere, which, in turn, affects radiation and climate. As the BDC cannot be directly measured, one has to infer its strength and trends indirectly. For instance, trace gas measurements allow the calculation of average transit times. Satellite measurements provide information on the distributions of trace gases for the entire stratosphere, with measurements of particularly long and dense coverage available for stratospheric water vapour (H2O). Although chemical processes and boundary conditions confound interpretation, the influence of CH4 oxidation on H2O is relatively straightforward, and thus H2O is an appealing tracer for transport analysis despite these caveats. In this work, we explore how mean age of air trends can be estimated from the combination of stratospheric H2O and CH4 data. We carry out different sensitivity studies with the Chemical Lagrangian Model of the Stratosphere (CLaMS) and focus on the analysis of the periods of 1990–2006 and 1990–2017. In particular, we assess the methodological uncertainties related to the two commonly-used approximations of (i) instantaneous stratospheric entry mixing ratio propagation, and (ii) constant correlation between mean age and the fractional release factor of methane. Our results show that the estimated mean age of air trends from the combination of observed stratospheric H2O and CH4 changes may be significantly affected by the assumed approximations. Depending on the investigated stratospheric region and the considered period, the error in estimated mean age of air decadal trends can be large – the discrepancies are up to 10 % per decade or even more at the lower stratosphere. For particular periods, the errors from the two approximations can lead to opposite effects, which may even cancel out. Finally, we propose an improvement to the approximation method by using an idealised age spectrum to propagate stratospheric entry mixing ratios. The findings of this work can be used for improving and assessing the uncertainties in stratospheric BDC trend estimation from global satellite measurements.

scholarly journals Trend differences in lower stratospheric water vapour between Boulder and the zonal mean and their role in understanding fundamental observational discrepancies

2018 ◽  
Vol 18 (11) ◽  
pp. 8331-8351 ◽  
Author(s):  
Stefan Lossow ◽  
Dale F. Hurst ◽  
Karen H. Rosenlof ◽  
Gabriele P. Stiller ◽  
Thomas von Clarmann ◽  
...  
Keyword(s):  
Water Vapour ◽  
Satellite Data ◽  
Middle Atmosphere ◽  
Michelson Interferometer ◽  
Lagrangian Model ◽  
Data Set ◽  
Temporal Behaviour ◽  
Model Simulations ◽  
Time Period ◽  
Stratospheric Water Vapour

Abstract. Trend estimates with different signs are reported in the literature for lower stratospheric water vapour considering the time period between the late 1980s and 2010. The NOAA (National Oceanic and Atmospheric Administration) frost point hygrometer (FPH) observations at Boulder (Colorado, 40.0° N, 105.2° W) indicate positive trends (about 0.1 to 0.45 ppmv decade−1). On the contrary, negative trends (approximately −0.2 to −0.1 ppmv decade−1) are derived from a merged zonal mean satellite data set for a latitude band around the Boulder latitude. Overall, the trend differences between the two data sets range from about 0.3 to 0.5 ppmv decade−1, depending on altitude. It has been proposed that a possible explanation for these discrepancies is a different temporal behaviour at Boulder and the zonal mean. In this work we investigate trend differences between Boulder and the zonal mean using primarily simulations from ECHAM/MESSy (European Centre for Medium-Range Weather Forecasts Hamburg/Modular Earth Submodel System) Atmospheric Chemistry (EMAC), WACCM (Whole Atmosphere Community Climate Model), CMAM (Canadian Middle Atmosphere Model) and CLaMS (Chemical Lagrangian Model of the Stratosphere). On shorter timescales we address this aspect also based on satellite observations from UARS/HALOE (Upper Atmosphere Research Satellite/Halogen Occultation Experiment), Envisat/MIPAS (Environmental Satellite/Michelson Interferometer for Passive Atmospheric Sounding) and Aura/MLS (Microwave Limb Sounder). Overall, both the simulations and observations exhibit trend differences between Boulder and the zonal mean. The differences are dependent on altitude and the time period considered. The model simulations indicate only small trend differences between Boulder and the zonal mean for the time period between the late 1980s and 2010. These are clearly not sufficient to explain the discrepancies between the trend estimates derived from the FPH observations and the merged zonal mean satellite data set. Unless the simulations underrepresent variability or the trend differences originate from smaller spatial and temporal scales than resolved by the model simulations, trends at Boulder for this time period should also be quite representative for the zonal mean and even other latitude bands. Trend differences for a decade of data are larger and need to be kept in mind when comparing results for Boulder and the zonal mean on this timescale. Beyond that, we find that the trend estimates for the time period between the late 1980s and 2010 also significantly differ among the simulations. They are larger than those derived from the merged satellite data set and smaller than the trend estimates derived from the FPH observations.

scholarly journals Evaluating stratospheric ozone and water vapour changes in CMIP6 models from 1850 to 2100

2021 ◽  
Vol 21 (6) ◽  
pp. 5015-5061
Author(s):  
James Keeble ◽  
Birgit Hassler ◽  
Antara Banerjee ◽  
Ramiro Checa-Garcia ◽  
Gabriel Chiodo ◽  
...  
Keyword(s):  
Water Vapour ◽  
21St Century ◽  
Tropospheric Ozone ◽  
Stratospheric Ozone ◽  
Volcanic Eruptions ◽  
Regional Patterns ◽  
Total Column Ozone ◽  
Mixing Ratios ◽  
The 1960S ◽  
Stratospheric Water Vapour

Abstract. Stratospheric ozone and water vapour are key components of the Earth system, and past and future changes to both have important impacts on global and regional climate. Here, we evaluate long-term changes in these species from the pre-industrial period (1850) to the end of the 21st century in Coupled Model Intercomparison Project phase 6 (CMIP6) models under a range of future emissions scenarios. There is good agreement between the CMIP multi-model mean and observations for total column ozone (TCO), although there is substantial variation between the individual CMIP6 models. For the CMIP6 multi-model mean, global mean TCO has increased from ∼ 300 DU in 1850 to ∼ 305 DU in 1960, before rapidly declining in the 1970s and 1980s following the use and emission of halogenated ozone-depleting substances (ODSs). TCO is projected to return to 1960s values by the middle of the 21st century under the SSP2-4.5, SSP3-7.0, SSP4-3.4, SSP4-6.0, and SSP5-8.5 scenarios, and under the SSP3-7.0 and SSP5-8.5 scenarios TCO values are projected to be ∼ 10 DU higher than the 1960s values by 2100. However, under the SSP1-1.9 and SSP1-1.6 scenarios, TCO is not projected to return to the 1960s values despite reductions in halogenated ODSs due to decreases in tropospheric ozone mixing ratios. This global pattern is similar to regional patterns, except in the tropics where TCO under most scenarios is not projected to return to 1960s values, either through reductions in tropospheric ozone under SSP1-1.9 and SSP1-2.6, or through reductions in lower stratospheric ozone resulting from an acceleration of the Brewer–Dobson circulation under other Shared Socioeconomic Pathways (SSPs). In contrast to TCO, there is poorer agreement between the CMIP6 multi-model mean and observed lower stratospheric water vapour mixing ratios, with the CMIP6 multi-model mean underestimating observed water vapour mixing ratios by ∼ 0.5 ppmv at 70 hPa. CMIP6 multi-model mean stratospheric water vapour mixing ratios in the tropical lower stratosphere have increased by ∼ 0.5 ppmv from the pre-industrial to the present-day period and are projected to increase further by the end of the 21st century. The largest increases (∼ 2 ppmv) are simulated under the future scenarios with the highest assumed forcing pathway (e.g. SSP5-8.5). Tropical lower stratospheric water vapour, and to a lesser extent TCO, shows large variations following explosive volcanic eruptions.

scholarly journals Evaluating stratospheric ozone and water vapor changes in CMIP6 models from 1850–2100

2020 ◽  
Author(s):  
James Keeble ◽  
Birgit Hassler ◽  
Antara Banerjee ◽  
Ramiro Checa-Garcia ◽  
Gabriel Chiodo ◽  
...  
Keyword(s):  
Water Vapour ◽  
21St Century ◽  
Tropospheric Ozone ◽  
Stratospheric Ozone ◽  
Volcanic Eruptions ◽  
Regional Patterns ◽  
Large Variability ◽  
Mixing Ratios ◽  
The 1960S ◽  
Stratospheric Water Vapour

Abstract. Stratospheric ozone and water vapour are key components of the Earth system, and past and future changes to both have important impacts on global and regional climate. Here we evaluate long-term changes in these species from the pre- industrial (1850) to the end of the 21st century in CMIP6 models under a range of future emissions scenarios. There is good agreement between the CMIP multi-model mean and observations, although there is substantial variation between the individual CMIP6 models. For the CMIP6 multi-model mean, global total column ozone (TCO) has increased from ∼300 DU in 1850 to ∼305 DU in 1960, before rapidly declining in the 1970s and 1980s following the use and emission of halogenated ozone depleting substances (ODSs). TCO is projected to return to 1960s values by the middle of the 21st century under the SSP2-4.5, SSP3-7.0, SSP4-3.4, SSP4-6.0 and SSP5-8.5 scenarios, and under the SSP3-7.0 and SSP5-8.5 scenarios TCO values are projected to be ∼10 DU higher than the 1960s values by 2100. However, under the SSP1-1.9 and SSP1-1.6 scenarios, TCO is not projected to return to the 1960s values despite reductions in halogenated ODSs due to decreases in tropospheric ozone mixing ratios. This global pattern is similar to regional patterns, except in the tropics where TCO under most scenarios is not projected to return to 1960s values, either through reductions in tropospheric ozone under SSP1-1.9 and SSP1-2.6, or through reductions in lower stratospheric ozone resulting from an acceleration of the Brewer-Dobson Circulation under other SSPs. CMIP6 multi-model mean stratospheric water vapour mixing ratios in the tropical lower stratosphere have increased by ∼0.5 ppmv from the pre-industrial to the present day and are projected to increase further by the end of the 21st century. The largest increases (∼2 ppmv) are simulated under the future scenarios with the highest assumed forcing pathway (e.g. SSP5-8.5). Both TCO and tropical lower stratospheric water vapour show large variability following explosive volcanic eruptions.

Direct Method of Measuring Stratospheric Water Vapour Mixing Ratios

Nature ◽  
1970 ◽  
Vol 227 (5260) ◽  
pp. 824-825 ◽  
Author(s):  
W. J. BURROUGHS ◽  
J. E. HARRIES
Keyword(s):  
Water Vapour ◽  
Direct Method ◽  
Mixing Ratios ◽  
Stratospheric Water Vapour

scholarly journals Can sampling biases explain the discrepancies between lower stratospheric water vapour trend estimates derived from the FPH observations at Boulder and a merged zonal mean satellite data set?

2018 ◽  
Author(s):  
Stefan Lossow ◽  
Dale F. Hurst ◽  
Karen H. Rosenlof ◽  
Gabriele P. Stiller ◽  
Thomas von Clarmann ◽  
...  
Keyword(s):  
Water Vapour ◽  
Satellite Data ◽  
Middle Atmosphere ◽  
Michelson Interferometer ◽  
Lagrangian Model ◽  
Data Set ◽  
Temporal Behaviour ◽  
Model Simulations ◽  
Time Period ◽  
Stratospheric Water Vapour

Abstract. Trend estimates with different signs are reported in the literature for lower stratospheric water vapour considering the time period between the late 1980s and 2010. The NOAA (National Oceanic and Atmospheric Administration) frost point hygrometer (FPH) observations at Boulder (Colorado, 40.0° N, 105.2° W) indicate positive trends (about 0.12 ppmv decade−1–0.45 ppmv decade−1). Contrary, negative trends (approximately −0.15 ppmv decade−1–−0.05  ppmv decade−1) are derived from a merged zonal mean satellite data set for a latitude band around the Boulder latitude. Overall, the trend differences between the two data sets range from about 0.25 ppmv decade−1 to 0.45 ppmv decade−1, depending on altitude. A possible explanation for these discrepancies is a different temporal behaviour at Boulder and the zonal mean, which simply indicates a sampling bias. In this work we investigate trend differences between Boulder and the zonal mean using primarily simulations from ECHAM/MESSy (European Centre for Medium-Range Weather Forecasts Hamburg/Modular Earth Submodel System) Atmospheric Chemistry (EMAC), WACCM (Whole Atmosphere Community Climate Model), CMAM (Canadian Middle Atmosphere Model) and CLaMS (Chemical Lagrangian Model of the Stratosphere). On shorter time scales we address this aspect also based on satellite observations from UARS/HALOE (Upper Atmosphere Research Satellite/Halogen Occultation Experiment), Envisat/MIPAS (Environmental Satellite/Michelson Interferometer for Passive Atmospheric Sounding) and Aura/MLS (Microwave Limb Sounder). Overall, both the simulations and observations exhibit trend differences between Boulder and the zonal mean. The differences are dependent on altitude and the time period considered. The model simulations indicate only small trend differences between Boulder and the zonal mean for the time period between the late 1980s and 2010. These are clearly not sufficient to explain the discrepancies between the trend estimates derived from the FPH observations and the merged zonal mean satellite data set. Unless the simulations underrepresent variability or the trend differences originate from smaller spatial and temporal scales than resolved by the model simulations, trends at Boulder for this time period should be quite representative also for the zonal mean and even other latitude bands. Trend differences for a decade of data are larger and need to be kept in mind when comparing results for Boulder and the zonal mean on this time scale. Beyond that, we find that the trend estimates for the time period between the late 1980s and 2010 also significantly differ among the simulations. They are larger than those derived from the merged satellite data set and smaller than the trend estimates derived from the FPH observations.

scholarly journals Effects of Strongly Enhanced Atmospheric Methane Concentrations in a Fully Coupled Chemistry-Climate Model

2020 ◽  
Author(s):  
Laura Stecher ◽  
Franziska Winterstein ◽  
Martin Dameris ◽  
Patrick Jöckel ◽  
Michael Ponater ◽  
...  
Keyword(s):  
Hydroxyl Radical ◽  
Water Vapour ◽  
Climate Sensitivity ◽  
Radiative Forcing ◽  
Climate Model ◽  
Atmospheric Methane ◽  
Climate Feedbacks ◽  
Mixing Ratios ◽  
Radiative Impact ◽  
Stratospheric Water Vapour

Abstract. In a previous study the quasi-instantaneous chemical impacts (rapid adjustments) of strongly enhanced methane (CH4) mixing ratios have been analyzed. However, to quantify the influence of the respective slow climate feedbacks on the chemical composition it is necessary to include the radiation driven temperature feedback. Therefore, we perform sensitivity simulations with doubled and fivefold present-day (year 2010) CH4 mixing ratios with the chemistry-climate model EMAC and include in a novel set-up a mixed layer ocean model to account for tropospheric warming. We find that the slow climate feedbacks counteract the reduction of the hydroxyl radical in the troposphere, which is caused by the strongly enhanced CH4 mixing ratios. Thereby also the resulting prolongation of the tropospheric CH4 lifetime is weakened compared to the quasi-instantaneous response considered previously. Changes in the stratospheric circulation evolve clearly with the warming of the troposphere. The Brewer-Dobson circulation strengthens, affecting the response of trace gases, such as ozone, water vapour and CH4 in the stratosphere, and also causing stratospheric temperature changes. In the middle and upper stratosphere, the increase of stratospheric water vapour is reduced with respect to the quasi-instantaneous response. Weaker increases of the hydroxyl radical cause the chemical depletion of CH4 to be less strongly enhanced and thus the in situ source of stratospheric water vapour as well. However, in the lower stratosphere water vapour increases more strongly when tropospheric warming is accounted for enlarging its overall radiative impact. The response of the stratospheric adjusted temperatures driven by slow climate feedbacks is dominated by these increases of stratospheric water vapour, as well as strongly decreased ozone mixing ratios above the tropical tropopause, which result from enhanced tropical upwelling. While rapid radiative adjustments from ozone and stratospheric water vapour make an essential contribution to the effective CH4 radiative forcing, the radiative impact of the respective slow feedbacks is rather moderate. In line with this, the climate sensitivity from CH4 changes in this chemistry-climate model setup is not significantly different from the climate sensitivity in carbon dioxide-driven simulations, provided that the CH4 effective radiative forcing includes the rapid adjustments from ozone and stratospheric water vapour changes.

scholarly journals Slow feedbacks resulting from strongly enhanced atmospheric methane mixing ratios in a chemistry–climate model with mixed-layer ocean

2021 ◽  
Vol 21 (2) ◽  
pp. 731-754
Author(s):  
Laura Stecher ◽  
Franziska Winterstein ◽  
Martin Dameris ◽  
Patrick Jöckel ◽  
Michael Ponater ◽  
...  
Keyword(s):  
Water Vapour ◽  
Climate Sensitivity ◽  
Radiative Forcing ◽  
Climate Model ◽  
Climate Feedbacks ◽  
Mixing Ratios ◽  
Mixed Layer Ocean ◽  
Radiative Impact ◽  
Set Up ◽  
Stratospheric Water Vapour

Abstract. In a previous study the quasi-instantaneous chemical impacts (rapid adjustments) of strongly enhanced methane (CH4) mixing ratios have been analysed. However, to quantify the influence of the respective slow climate feedbacks on the chemical composition it is necessary to include the radiation-driven temperature feedback. Therefore, we perform sensitivity simulations with doubled and quintupled present-day (year 2010) CH4 mixing ratios with the chemistry–climate model EMAC (European Centre for Medium-Range Weather Forecasts, Hamburg version – Modular Earth Submodel System (ECHAM/MESSy) Atmospheric Chemistry) and include in a novel set-up a mixed-layer ocean model to account for tropospheric warming. Strong increases in CH4 lead to a reduction in the hydroxyl radical in the troposphere, thereby extending the CH4 lifetime. Slow climate feedbacks counteract this reduction in the hydroxyl radical through increases in tropospheric water vapour and ozone, thereby dampening the extension of CH4 lifetime in comparison with the quasi-instantaneous response. Changes in the stratospheric circulation evolve clearly with the warming of the troposphere. The Brewer–Dobson circulation strengthens, affecting the response of trace gases, such as ozone, water vapour and CH4 in the stratosphere, and also causing stratospheric temperature changes. In the middle and upper stratosphere, the increase in stratospheric water vapour is reduced with respect to the quasi-instantaneous response. We find that this difference cannot be explained by the response of the cold point and the associated water vapour entry values but by a weaker strengthening of the in situ source of water vapour through CH4 oxidation. However, in the lower stratosphere water vapour increases more strongly when tropospheric warming is accounted for, enlarging its overall radiative impact. The response of the stratosphere adjusted temperatures driven by slow climate feedbacks is dominated by these increases in stratospheric water vapour as well as strongly decreased ozone mixing ratios above the tropical tropopause, which result from enhanced tropical upwelling. While rapid radiative adjustments from ozone and stratospheric water vapour make an essential contribution to the effective CH4 radiative forcing, the radiative impact of the respective slow feedbacks is rather moderate. In line with this, the climate sensitivity from CH4 changes in this chemistry–climate model set-up is not significantly different from the climate sensitivity in carbon-dioxide-driven simulations, provided that the CH4 effective radiative forcing includes the rapid adjustments from ozone and stratospheric water vapour changes.

scholarly journals Quantification of water vapour transport from the Asian monsoon to the stratosphere

2019 ◽  
Vol 19 (13) ◽  
pp. 8947-8966 ◽  
Author(s):  
Matthias Nützel ◽  
Aurélien Podglajen ◽  
Hella Garny ◽  
Felix Ploeger
Keyword(s):  
Mass Transport ◽  
Water Vapour ◽  
Asian Monsoon ◽  
Lagrangian Model ◽  
Vapour Transport ◽  
Monsoon Region ◽  
Asian Monsoon Region ◽  
Upper Troposphere ◽  
Water Vapour Transport ◽  
Stratospheric Water Vapour

Abstract. Numerous studies have presented evidence that the Asian summer monsoon anticyclone substantially influences the distribution of trace gases – including water vapour – in the upper troposphere and lower stratosphere (e.g. Santee et al., 2017). Stratospheric water vapour in turn strongly affects surface climate (see e.g. Solomon et al., 2010). Here, we analyse the characteristics of water vapour transport from the upper troposphere in the Asian monsoon region to the stratosphere employing a multiannual simulation with the chemistry-transport model CLaMS (Chemical Lagrangian Model of the Stratosphere). This simulation is driven by meteorological data from ERA-Interim and features a water vapour tagging that allows us to assess the contributions of different upper tropospheric source regions to the stratospheric water vapour budget. Our results complement the analysis of air mass transport through the Asian monsoon anticyclone by Ploeger et al. (2017). The results show that the transport characteristics for water vapour are mainly determined by the bulk mass transport from the Asian monsoon region. Further, we find that, although the relative contribution from the Asian monsoon region to water vapour in the deep tropics is rather small (average peak contribution of 14 % at 450 K), the Asian monsoon region is very efficient in transporting water vapour to this region (when judged according to its comparatively small spatial extent). With respect to the Northern Hemisphere extratropics, the Asian monsoon region is much more impactful and efficient regarding water vapour transport than e.g. the North American monsoon region (averaged maximum contributions at 400 K of 29 % versus 6.4 %).

scholarly journals Quantification of water vapour transport from the Asian monsoon to the stratosphere

2019 ◽  
Author(s):  
Matthias Nützel ◽  
Aurelien Podglajen ◽  
Hella Garny ◽  
Felix Ploeger
Keyword(s):  
Mass Transport ◽  
Water Vapour ◽  
Asian Monsoon ◽  
Lagrangian Model ◽  
Vapour Transport ◽  
Monsoon Region ◽  
Asian Monsoon Region ◽  
Upper Troposphere ◽  
Water Vapour Transport ◽  
Stratospheric Water Vapour

Abstract. Numerous studies have presented evidence that the Asian summer monsoon anticyclone substantially influences the distribution of trace gases – including water vapour – in the upper troposphere and lower stratosphere (e.g. Santee et al., 2017). Stratospheric water vapour in turn, is strongly affecting surface climate (cf. e.g. Solomon et al., 2010). Here, we analyse the characteristics of water vapour transport from the upper troposphere in the Asian monsoon region to the stratosphere employing a multiannual simulation with the chemistry-transport model CLaMS (Chemical Lagrangian Model of the Stratosphere). This simulation is driven by meteorological data from ERA-Interim and features a water vapour tagging that allows us to assess the contributions of different upper tropospheric source regions to the stratospheric water vapour budget. Our results complement the analysis of air mass transport through the Asian monsoon anticyclone by Ploeger et al. (2017). The results show that the transport characteristics for water vapour are mainly determined by the bulk mass transport from the Asian monsoon region. Further, we find that, although the relative contribution from the Asian monsoon region to water vapour in the deep tropics is rather small (average peak contribution of 14 % at 450 K), the Asian monsoon region is very efficient in transporting water vapour to this region (when judged according to its comparatively small spatial extent). With respect to the Northern Hemisphere extratropics, the Asian monsoon region is much more impactful and efficient regarding water vapour transport than e.g. the North American monsoon region (averaged maximum contributions at 400 K of 29 % vs. 6.4 %).

scholarly journals Sensitivity of polar stratospheric cloud formation to changes in water vapour and temperature

2015 ◽  
Vol 15 (13) ◽  
pp. 17743-17796 ◽  
Author(s):  
F. Khosrawi ◽  
J. Urban ◽  
S. Lossow ◽  
G. Stiller ◽  
K. Weigel ◽  
...  
Keyword(s):  
Water Vapour ◽  
Recent Decade ◽  
Sensitivity Study ◽  
Cloud Formation ◽  
The Arctic ◽  
Polar Regions ◽  
Mixing Ratios ◽  
Polar Stratospheric Cloud ◽  
The Tropics ◽  
Stratospheric Water Vapour

Abstract. More than a decade ago it was suggested that a cooling of stratospheric temperatures by 1 K or an increase of 1 ppmv of stratospheric water vapour could promote denitrification, the permanent removal of nitrogen species from the stratosphere by solid polar stratospheric cloud (PSC) particles. In fact, during the two Arctic winters 2009/10 and 2010/11 the strongest denitrification in the recent decade was observed. Sensitivity studies along air parcel trajectories are performed to test how a future stratospheric water vapour (H2O) increase of 1 ppmv or a temperature decrease of 1 K would affect PSC formation. We perform our study based on measurements made during the Arctic winter 2010/11. Air parcel trajectories were calculated 6 days backward in time based on PSCs detected by CALIPSO (Cloud Aerosol Lidar and Infrared Pathfinder satellite observations). The sensitivity study was performed on single trajectories as well as on a trajectory ensemble. The sensitivity study shows a clear prolongation of the potential for PSC formation and PSC existence when the temperature in the stratosphere is decreased by 1 K and water vapour is increased by 1 ppmv. Based on 15 years of satellite measurements (2000–2014) from UARS/HALOE, Envisat/MIPAS, Odin/SMR, Aura/MLS, Envisat/SCIAMACHY and SCISAT/ACE-FTS it is further investigated if there is a decrease in temperature and/or increase of water vapour (H2O) observed in the polar regions similar to that observed at midlatitudes and in the tropics. Although in the polar regions no significant trend is found in the lower stratosphere, we found from the observations a correlation between cold winters and enhanced water vapour mixing ratios.

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