Review of : The Impact of Volcanic Eruptions of Different Magnitude on Stratospheric Water Vapour in the Tropics by Kroll et al. (https://doi.org/10.5194/acp-2020-1191)

Abstract. Volcanic eruptions increase the stratospheric water vapour (SWV) entry via long wave heating through the aerosol layer in the cold point region, and this additional SWV alters the atmospheric energy budget. We analyze tropical volcanic eruptions of different eruption strengths with sulfur (S) injections ranging from 2.5 Tg S up to 40 Tg S using EVAens, the 100-member ensemble of the Max Planck Institute – Earth System Model in its low resolution configuration (MPI-ESM-LR) with artificial volcanic forcing generated by the Easy Volcanic Aerosol (EVA) tool. Significant increases in SWV are found for the mean over all ensemble members from 2.5 Tg S onward ranging between [5,160] %, while for single ensemble members the standard deviation between the control run members (0 Tg S) is larger than SWV increase of single ensemble members for the eruption strengths up to 20 Tg S. A historical simulation using observation based forcing files of the Mt. Pinatubo eruption, which was estimated to have emitted (7.5 &pm; 2.5) Tg S, returns SWV increases slightly higher than the 10 Tg S EVAens simulations due to differences in the aerosol profile shape. An additional amplification of the tape recorder signal is also apparent, which is not present in the 10 Tg S run. These differences underline that it is not only the eruption volume, but also the aerosol layer shape and location with respect to the cold point that have to be considered for post-eruption SWV increases. The additional tropical clear sky SWV forcing for the different eruption strengths amounts to [0.02, 0.65] W/m2, ranging between [2.5, 4] percent of the aerosol radiative forcing in the 10 Tg S scenario. The monthly cold point temperature increases leading to the SWV increase are not linear with respect to AOD nor is the corresponding SWV forcing, among others, due to hysteresis effects, seasonal dependencies, aerosol profile heights, and feedbacks. However, knowledge of the cold point temperature increase allows for an estimation of SWV increases with a 12 % increase per Kelvin increase in mean cold point temperature, and yearly averages show an approximately linear behaviour in the cold point warming and SWV forcing with respect to the AOD.

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Linking the uncertainty in simulated arctic ozone losses to modelling of tropical stratospheric water vapour

10.5194/acp-2018-310 ◽

2018 ◽

Author(s):

Laura Thölix ◽

Alexey Karpechko ◽

Leif Backman ◽

Rigel Kivi

Keyword(s):

Water Vapour ◽

Climate Models ◽

Polar Vortex ◽

The Arctic ◽

Ozone Loss ◽

Tropical Tropopause ◽

Water Vapour Concentration ◽

Vapour Concentration ◽

The Impact ◽

Stratospheric Water Vapour

Abstract. Stratospheric water vapor plays a key role in radiative and chemical processes, it e.g. influences the chemical ozone loss via controlling the polar stratospheric cloud formation in the polar stratosphere. The amount of water entering the stratosphere through the tropical tropopause differs substantially between chemistry-climate models. This is because the present-day models have difficulties in capturing the whole complexity of processes that control the water transport across the tropopause. As a result there are large differences in the stratospheric water vapour between the models. In this study we investigate the sensitivity of simulated Arctic ozone loss to the amount of water, which enters the stratosphere through the tropical tropopause. We used a chemical transport model, FinROSE-CTM, forced by ERA-Interim meteorology. The water vapour concentration in the tropical tropopause was varied between 0.5 and 1.6 times the concentration in ERA-Interim, which is similar to the range seen in chemistry climate models. The water vapour changes in the tropical tropopause led to about 1.5 and 2 ppm more water vapour in the Arctic polar vortex compared to the ERA-Interim, respectively. We found that the impact of water vapour changes on ozone loss in the Arctic polar vortex depend on the meteorological conditions. Polar stratospheric clouds form in the cold conditions within the Arctic vortex, and chlorine activation on their surface lead to ozone loss. If the cold conditions persist long enough (e.g. in 2010/11), the chlorine activation is nearly complete. In this case addition of water vapour to the stratosphere increased the formation of ICE clouds, but did not increase the chlorine activation and ozone destruction significantly. In the warm winter 2012/13 the impact of water vapour concentration on ozone loss was small, because the ozone loss was mainly NOx induced. In intermediately cold conditions, e.g. 2013/14, the effect of added water vapour was more prominent than in the other studied winters. The results show that the simulated water vapour concentration in the tropical tropopause has a significant impact on the Arctic ozone loss and deserves attention in order to improve future projections of ozone layer recovery.

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Trends and variability of midlatitude stratospheric water vapour deduced from the re-evaluated Boulder balloon series and HALOE

Atmospheric Chemistry and Physics ◽

10.5194/acp-8-1391-2008 ◽

2008 ◽

Vol 8 (5) ◽

pp. 1391-1402 ◽

Cited By ~ 83

Author(s):

M. Scherer ◽

H. Vömel ◽

S. Fueglistaler ◽

S. J. Oltmans ◽

J. Staehelin

Keyword(s):

Water Vapour ◽

Linear Trend ◽

Potential Temperature ◽

Data Series ◽

Explanatory Variables ◽

Time Period ◽

Corrected Data ◽

Instrumental Bias ◽

The Tropics ◽

Stratospheric Water Vapour

Abstract. This paper presents an updated trend analysis of water vapour in the lower midlatitude stratosphere from the Boulder balloon-borne NOAA frostpoint hygrometer measurements and from the Halogen Occulation Experiment (HALOE). Two corrections for instrumental bias are applied to homogenise the frostpoint data series, and a quality assessment of all soundings after 1991 is presented. Linear trend estimates based on the corrected data for the period 1980–2000 are up to 40% lower than previously reported. Vertically resolved trends and variability are calculated with a multi regression analysis including the quasi-biennal oscillation and equivalent latitude as explanatory variables. In the range of 380 to 640 K potential temperature (≈14 to 25 km), the frostpoint data from 1981 to 2006 show positive linear trends between 0.3±0.3 and 0.7±0.1%/yr. The same dataset shows trends between −0.2±0.3 and 1.0±0.3%/yr for the period 1992 to 2005. HALOE data over the same time period suggest negative trends ranging from −1.1±0.2 to −0.1±0.1%/yr. In the lower stratosphere, a rapid drop of water vapour is observed in 2000/2001 with little change since. At higher altitudes, the transition is more gradual, with slowly decreasing concentrations between 2001 and 2007. This pattern is consistent with a change induced by a drop of water concentrations at entry into the stratosphere. Previously noted differences in trends and variability between frostpoint and HALOE remain for the homogenised data. Due to uncertainties in reanalysis temperatures and stratospheric transport combined with uncertainties in observations, no quantitative inference about changes of water entering the stratosphere in the tropics could be made with the mid latitude measurements analysed here.

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

Atmospheric Chemistry and Physics ◽

10.5194/acp-21-5015-2021 ◽

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.

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

10.5194/acp-2019-1202 ◽

2020 ◽

Cited By ~ 1

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.

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Volcanic aerosol heating in the tropical tropopause region and associated water vapour changes

10.5194/egusphere-egu21-12318 ◽

2021 ◽

Author(s):

Clarissa Kroll ◽

Hauke Schmidt ◽

Claudia Timmreck

Keyword(s):

Water Vapour ◽

Volcanic Eruptions ◽

Aerosol Layer ◽

Volcanic Aerosol ◽

Surface Warming ◽

Tropical Tropopause ◽

Tropopause Region ◽

Cold Point ◽

The Impact

Large volcanic eruptions affect the distribution of atmospheric water vapour, for instance through cooling of the surface, warming of the lowermost stratosphere, and increasing the upwelling in the tropical tropopause region.To better understand the volcanic impact on the tropical tropopause region and associated changes in the water vapour distribution in the stratosphere we employ a combination of short term convection-resolving global simulations with ICON and long term low resolution ensemble simulations with the MPI-ESM1.2-LR EVAens, both with prescribed volcanic forcing. With the EVAens a long term statistical analysis of the water vapour trends during the build-up and decay of a volcanic aerosol layer is made possible. The impact of the heating in the cold point regions is studied for five different eruption magnitudes. Stratospheric water vapour changes are analyzed in simulations with synthetic and observation based aerosol profiles showing that the distance of the aerosol profile from the cold point region can be more important for the water vapour entry into the stratosphere than the emitted amount of sulfur.Whereas the EVAens is ideal to investigate the slow ascent of water vapour into the stratosphere the 10 km high resolution simulations with ICON allow insights into the convective changes after volcanic eruptions going beyond the limitations parameterizations usually impose on the model data.

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Impact of major volcanic eruptions on stratospheric water vapour

Atmospheric Chemistry and Physics ◽

10.5194/acp-16-6547-2016 ◽

2016 ◽

Vol 16 (10) ◽

pp. 6547-6562 ◽

Cited By ~ 11

Author(s):

Michael Löffler ◽

Sabine Brinkop ◽

Patrick Jöckel

Keyword(s):

Water Vapour ◽

Atmospheric Chemistry ◽

Southern Oscillation ◽

Volcanic Eruptions ◽

The Philippines ◽

Integrated Modelling ◽

South Asian Summer Monsoon ◽

Mount Pinatubo ◽

Long Wave ◽

Stratospheric Water Vapour

Abstract. Volcanic eruptions can have a significant impact on the Earth's weather and climate system. Besides the subsequent tropospheric changes, the stratosphere is also influenced by large eruptions. Here changes in stratospheric water vapour after the two major volcanic eruptions of El Chichón in Mexico in 1982 and Mount Pinatubo on the Philippines in 1991 are investigated with chemistry–climate model simulations. This study is based on two simulations with specified dynamics of the European Centre for Medium-Range Weather Forecasts Hamburg – Modular Earth Submodel System (ECHAM/MESSy) Atmospheric Chemistry (EMAC) model, performed within the Earth System Chemistry integrated Modelling (ESCiMo) project, of which only one includes the long-wave volcanic forcing through prescribed aerosol optical properties. The results show a significant increase in stratospheric water vapour induced by the eruptions, resulting from increased heating rates and the subsequent changes in stratospheric and tropopause temperatures in the tropics. The tropical vertical advection and the South Asian summer monsoon are identified as sources for the additional water vapour in the stratosphere. Additionally, volcanic influences on tropospheric water vapour and El Niño–Southern Oscillation (ENSO) are evident, if the long-wave forcing is strong enough. Our results are corroborated by additional sensitivity simulations of the Mount Pinatubo period with reduced nudging and reduced volcanic aerosol extinction.

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The climatic effects of the direct injection of water vapour into the stratosphere by large volcanic eruptions

Atmospheric Chemistry and Physics ◽

10.5194/acp-9-6109-2009 ◽

2009 ◽

Vol 9 (16) ◽

pp. 6109-6118 ◽

Cited By ~ 19

Author(s):

M. M. Joshi ◽

G. S. Jones

Keyword(s):

Water Vapour ◽

Climate Model ◽

Direct Injection ◽

Volcanic Eruptions ◽

Pyroclastic Flows ◽

Aerosol Formation ◽

Climatic Effects ◽

Climatic Cooling ◽

Large Volcanic Eruptions ◽

Stratospheric Water Vapour

Abstract. We describe a novel mechanism that can significantly lower the amplitude of the climatic response to certain large volcanic eruptions and examine its impact with a coupled ocean-atmosphere climate model. If sufficiently large amounts of water vapour enter the stratosphere, a climatically significant amount of water vapour can be left over in the lower stratosphere after the eruption, even after sulphate aerosol formation. This excess stratospheric humidity warms the tropospheric climate, and acts to balance the climatic cooling induced by the volcanic aerosol, especially because the humidity anomaly lasts for a period that is longer than the residence time of aerosol in the stratosphere. In particular, northern hemisphere high latitude cooling is reduced in magnitude. We discuss this mechanism in the context of the discrepancy between the observed and modelled cooling following the Krakatau eruption in 1883. We hypothesize that moist coignimbrite plumes caused by pyroclastic flows travelling over ocean rather than land, resulting from an eruption close enough to the ocean, might provide the additional source of stratospheric water vapour.

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Trends and variability of midlatitude stratospheric water vapour deduced from the re-evaluated Boulder balloon series and HALOE

Atmospheric Chemistry and Physics Discussions ◽

10.5194/acpd-7-14511-2007 ◽

2007 ◽

Vol 7 (5) ◽

pp. 14511-14542 ◽

Cited By ~ 3

Author(s):

M. Scherer ◽

H. Vömel ◽

S. Fueglistaler ◽

S. J. Oltmans ◽

J. Staehelin

Keyword(s):

Water Vapour ◽

Linear Trend ◽

Potential Temperature ◽

Data Series ◽

Explanatory Variables ◽

Time Period ◽

Corrected Data ◽

Instrumental Bias ◽

The Tropics ◽

Stratospheric Water Vapour

Abstract. This paper presents an updated trend analysis of water vapour in the lower midlatitude stratosphere from the Boulder balloon-borne NOAA frostpoint hygrometer measurements and from the Halogen Occulation Experiment (HALOE). Two corrections for instrumental bias are applied to homogenise the frostpoint data series, and a quality assessment of all soundings after 1991 is presented. Linear trend estimates based on the corrected data for the period 1980–2000 are up to 40% lower than previously reported. Vertically resolved trends and variability are calculated with a multi regression analysis including the quasi-biennal oscillation and equivalent latitude as explanatory variables. In the range of 380 to 640 K potential temperature (≈14 to 25 km), the frostpoint data from 1981 to 2006 show positive linear trends between 0.3± 0.3 and 0.7±0.1%/yr. The same dataset shows trends between −0.2±0.3 and 1.0±0.3%/yr for the period 1992 to 2005. HALOE data over the same time period suggest negative trends ranging from −1.1±0.2 to −0.1±0.1%/yr. In the lower stratosphere, a rapid drop of water vapour is observed in 2000/2001 with little change since. At higher altitudes, the transition is more gradual, with slowly decreasing concentrations between 2001 and 2007. This pattern is consistent with a change induced by a drop of water concentrations at entry into the stratosphere. Previously noted differences in trends and variability between frostpoint and HALOE remain for the homogenised data. Due to uncertainties in reanalysis temperatures and stratospheric transport combined with uncertainties in observations, no quantitative inference about changes of water entering the stratosphere in the tropics could be made with the mid latitude measurements analysed here.

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