scholarly journals Persistence of moist plumes from overshooting convection in the Asian monsoon anticyclone

2021 ◽  
Author(s):  
Sergey Khaykin ◽  
Elizabeth Moyer ◽  
Martina Krämer ◽  
Benjamin Clouser ◽  
Silvia Bucci ◽  
...  
Keyword(s):  
Water Vapour ◽  
Asian Monsoon ◽  
Lower Stratosphere ◽  
Background Level ◽  
Isotopic Signature ◽  
Surprising Result ◽  
Airborne Measurements ◽  
Mixing Ratios ◽  
Ice Water

Abstract. The Asian Monsoon Anticyclone (AMA) represents the wettest region in the lower stratosphere (LS) and is the key contributor to the global annual maximum in LS water vapour. While the AMA wet pool is linked with persistent convection in the region and horizontal confinement of the anticyclone, there remain ambiguities regarding the role of tropopause-overshooting convection in maintaining the regional LS water vapour maximum. This study tackles this issue using a unique set of observations from onboard the high-altitude M55-Geophysica aircraft deployed in Nepal in Summer 2017 within the EU StratoClim project. We use a combination of airborne measurements (water vapour, ice water, water isotopes, cloud backscatter) together with ensemble trajectory modeling coupled with satellite observations to characterize the processes controlling water vapour and clouds in the confined lower stratosphere (CLS) of AMA. Our analysis puts in evidence the dual role of overshooting convection, which may lead to hydration or dehydration depending on the synoptic-scale tropopause temperatures in AMA. We show that all of the observed CLS water vapour enhancements are traceable to convective events within AMA and furthermore bear an isotopic signature of the overshooting process. A surprising result is that the plumes of moist air with mixing ratios nearly twice the background level can persist for weeks whilst recirculating within the anticyclone, without being subject to irreversible dehydration through ice settling. Our findings highlight the importance of convection and recirculation within AMA for the transport of water into the stratosphere.

scholarly journals An aircraft gas chromatograph–mass spectrometer System for Organic Fast Identification Analysis (SOFIA): design, performance and a case study of Asian monsoon pollution outflow

2017 ◽  
Vol 10 (12) ◽  
pp. 5089-5105 ◽  
Author(s):  
Efstratios Bourtsoukidis ◽  
Frank Helleis ◽  
Laura Tomsche ◽  
Horst Fischer ◽  
Rolf Hofmann ◽  
...  
Keyword(s):  
Time Resolution ◽  
Asian Monsoon ◽  
Electrical Safety ◽  
Back Trajectory ◽  
Airborne Measurements ◽  
Mixing Ratios ◽  
Fast Identification ◽  
Chemistry Research ◽  
Identification Analysis

Abstract. Volatile organic compounds (VOCs) are important for global air quality and oxidation processes in the troposphere. In addition to ground-based measurements, the chemical evolution of such species during transport can be studied by performing in situ airborne measurements. Generally, aircraft instrumentation needs to be sensitive, robust and sample at higher frequency than ground-based systems while their construction must comply with rigorous mechanical and electrical safety standards. Here, we present a new System for Organic Fast Identification Analysis (SOFIA), which is a custom-built fast gas chromatography–mass spectrometry (GC-MS) system with a time resolution of 2–3 min and the ability to quantify atmospheric mixing ratios of halocarbons (e.g. chloromethanes), hydrocarbons (e.g isoprene), oxygenated VOCs (acetone, propanal, butanone) and aromatics (e.g. benzene, toluene) from sub-ppt to ppb levels. The relatively high time resolution is the result of a novel cryogenic pre-concentration unit which rapidly cools (∼ 6 °C s−1) the sample enrichment traps to −140 °C, and a new chromatographic oven designed for rapid cooling rates (∼ 30 °C s−1) and subsequent thermal stabilization. SOFIA was installed in the High Altitude and Long Range Research Aircraft (HALO) for the Oxidation Mechanism Observations (OMO) campaign in August 2015, aimed at investigating the Asian monsoon pollution outflow in the tropical upper troposphere. In addition to a comprehensive instrument characterization we present an example monsoon plume crossing flight as a case study to demonstrate the instrument capability. Hydrocarbon, halocarbon and oxygenated VOC data from SOFIA are compared with mixing ratios of carbon monoxide (CO) and methane (CH4), used to define the pollution plume. By using excess (ExMR) and normalized excess mixing ratios (NEMRs) the pollution could be attributed to two air masses of distinctly different origin, identified by back-trajectory analysis. This work endorses the use of SOFIA for aircraft operation and demonstrates the value of relatively high-frequency, multicomponent measurements in atmospheric chemistry research.

scholarly journals Brominated VSLS and their influence on ozone under a changing climate

2017 ◽  
Vol 17 (18) ◽  
pp. 11313-11329 ◽  
Author(s):  
Stefanie Falk ◽  
Björn-Martin Sinnhuber ◽  
Gisèle Krysztofiak ◽  
Patrick Jöckel ◽  
Phoebe Graf ◽  
...  
Keyword(s):  
21St Century ◽  
Atmospheric Chemistry ◽  
Lower Stratosphere ◽  
Atmospheric Transport ◽  
Stratospheric Ozone ◽  
Chemical Transformations ◽  
Mixing Ratios ◽  
Ocean Atmosphere ◽  
The Impact

Abstract. Very short-lived substances (VSLS) contribute as source gases significantly to the tropospheric and stratospheric bromine loading. At present, an estimated 25 % of stratospheric bromine is of oceanic origin. In this study, we investigate how climate change may impact the ocean–atmosphere flux of brominated VSLS, their atmospheric transport, and chemical transformations and evaluate how these changes will affect stratospheric ozone over the 21st century. Under the assumption of fixed ocean water concentrations and RCP6.0 scenario, we find an increase of the ocean–atmosphere flux of brominated VSLS of about 8–10 % by the end of the 21st century compared to present day. A decrease in the tropospheric mixing ratios of VSLS and an increase in the lower stratosphere are attributed to changes in atmospheric chemistry and transport. Our model simulations reveal that this increase is counteracted by a corresponding reduction of inorganic bromine. Therefore the total amount of bromine from VSLS in the stratosphere will not be changed by an increase in upwelling. Part of the increase of VSLS in the tropical lower stratosphere results from an increase in the corresponding tropopause height. As the depletion of stratospheric ozone due to bromine depends also on the availability of chlorine, we find the impact of bromine on stratospheric ozone at the end of the 21st century reduced compared to present day. Thus, these studies highlight the different factors influencing the role of brominated VSLS in a future climate.

scholarly journals Impact of tropical land convection on the water vapour budget in the Tropical Tropopause Layer

2013 ◽  
Vol 13 (12) ◽  
pp. 33055-33087
Author(s):  
F. Carminati ◽  
P. Ricaud ◽  
J.-P. Pommereau ◽  
E. Rivière ◽  
S. Khaykin ◽  
...  
Keyword(s):  
Water Vapour ◽  
Diurnal Cycle ◽  
Lower Stratosphere ◽  
Regional Scale ◽  
Maritime Continent ◽  
Tropical Tropopause Layer ◽  
Tropical Tropopause ◽  
Geographical Variations ◽  
Water Vapour Concentration ◽  
Ice Water

Abstract. The tropical deep overshooting convection is known to be most intense above continental areas such as South America, Africa and the maritime continent. However, its impact on the Tropical Tropopause Layer (TTL) at global scale remains debated. In our analysis, we use the 8 yr Microwave Limb Sounder (MLS) water vapour (H2O), cloud ice water content (IWC) and temperature datasets from 2005 to date, to highlight the interplays between these parameters and their role in the water vapour variability in the TTL, separately in the northern and southern tropics. The water vapour concentration is displaying a systematic diurnal cycle with a night-time peak in the tropical Upper Troposphere (pressure ≥146 hPa) and the opposite in the TTL (121 to 68 hPa) and the tropical Lower Stratosphere (pressure ≤56 hPa), of larger amplitude above continents than continental-oceanic areas such as the maritime continent or full oceanic areas such as the Western Pacific. In addition, the amplitude of the diurnal cycle is found systematically larger (5–10%) in the southern than in the northern tropics during their respective summer, indicative of a more vigorous convective intensity in the south. Using a regional scale approach, we investigate the geographical variations of mechanisms linked to the H2O variability. In summary, the MLS water vapour, ice water cloud and temperature observations are demonstrating a clear contribution of TTL and lower stratosphere moistening by ice crystals overshooting updrafts over land tropical regions and the much greater efficiency of the process in the Southern Hemisphere.

Investigation of transport in the northern lowermost stratosphere between spring and fall using airborne in situ tracer measurements

2020 ◽  
Author(s):  
Andrea Rau ◽  
Valentin Lauther ◽  
Johannes Wintel ◽  
Emil Gehardt ◽  
Peter Hoor ◽  
...  
Keyword(s):  
Time Scales ◽  
Asian Monsoon ◽  
Lagrangian Model ◽  
Mixing Ratios ◽  
Tropical Tropopause ◽  
Research Aircraft ◽  
Transport And Mixing ◽  
The University

<p>Over the course of the summer, when the subtropical jet is weakest, quasi-isentropic transport of young air from the troposphere and the tropical tropopause layer into the northern hemisphere (NH) lowermost stratosphere (LMS) is increased resulting in a drastic change of LMS chemical composition between spring and fall. The focus of this work is on the role of different transport paths into the NH LMS, including outflow from the Asian Monsoon, and their associated time scales of transport and mixing.<br><br>We present and analyse in situ measurements of CO<sub>2</sub> and various long-lived tracers obtained during three recent aircraft campaigns encompassing over 40 research flights in the NH UTLS during winter/spring, summer, and fall. The POLSTRACC/GW-LCYCLE/SALSA campaign probed the northern high latitude LMS in winter/spring 2016, deploying the German research aircraft HALO from Kiruna (Sweden) and from Germany. The second campaign deployed the M55 Geophysica research aircraft in July/August 2017 from Kathmandu, Nepal, in the frame of the EU-funded project StratoClim (Stratospheric and upper tropospheric processes for better Climate predications) in order to probe in situ for the first time the inside of the Asian Monsoon anticyclone. Roughly two months later the WISE (Wave-driven ISentropic Exchange) campaign deployed again HALO from Shannon (Ireland) in September and October 2017 to investigate isentropic transport and mixing in the NH LMS.<br><br>The University of Wuppertal measured CO<sub>2</sub> and a suite of long-lived tracers on each aircraft. On the Geophysica, the measurements were made with the HAGAR (High Altitude Gas AnalyzeR) instrument. On HALO, a recently developed extended 5-channel version, HAGAR-V, was flown, which in addition measured a suite of short-lived tracers by GC coupled with a mass spectrometer. The University of Mainz measured N2O and CO on HALO using laser absorption techniques. For our analysis we use mixing ratios of CO<sub>2</sub>, SF<sub>6</sub>, CFC-11, CFC-12, and N<sub>2</sub>O.<br><br>Owing to their different lifetimes, tropospheric growth (for SF<sub>6</sub>) and a seasonal cycle (for CO<sub>2</sub>), the LMS distributions of these long-lived trace gases and their development between spring and fall contain key information about the origin and mean stratospheric age of LMS air as well as time scales of rapid isentropic transport and mixing. The analysis of tracer measurements is complemented by simulations with the Chemical Lagrangian Model of the Stratosphere (CLaMS) providing information on age of air spectra and fractions of origin from specific surface regions, allowing in particular to assess the role of the Asian Monsoon in determining the composition of the NH LMS in fall.</p>

On the role of water vapour in the heat balance of the antarctic lower stratosphere

1991 ◽  
Vol 14 (3) ◽  
pp. 315-318
Author(s):  
S. Palermi ◽  
G. Pitari ◽  
G. Visconti ◽  
E. Mancini
Keyword(s):  
Water Vapour ◽  
Heat Balance ◽  
Lower Stratosphere ◽  
The Antarctic ◽  
The Heat Balance

scholarly journals Brominated VSLS and their influence on ozone under a changing climate

2017 ◽  
Author(s):  
Stefanie Falk ◽  
Björn-Martin Sinnhuber ◽  
Gisèle Krysztofiak ◽  
Patrick Jöckel ◽  
Phoebe Graf ◽  
...  
Keyword(s):  
21St Century ◽  
Atmospheric Chemistry ◽  
Lower Stratosphere ◽  
Atmospheric Transport ◽  
Stratospheric Ozone ◽  
Chemical Transformations ◽  
Mixing Ratios ◽  
Ocean Atmosphere ◽  
The Impact

Abstract. Very short-lived source gases (VSLS) contribute significantly to the tropospheric and stratospheric bromine loading. At present, an estimated 25 % of stratospheric bromine is of oceanic origin. In this study, we investigate how climate change may impact the ocean-atmosphere flux of brominated VSLS, their atmospheric transport, chemical transformations, and evaluate how these changes will affect stratospheric ozone over the 21st century. Under the assumption of fixed ocean water concentrations and RCP6.0 scenario, we find an increase of the ocean-atmosphere flux of brominated VSLS of about 8–10 % by the end of the 21st century compared to present day. A decrease in the tropospheric mixing ratios of VSLS and an increase in the lower stratosphere are attributed to changes in atmospheric chemistry and transport. Our model simulations reveal that, in line with the reduction in the troposphere, the total amount of bromine from VSLS in the stratosphere will decrease during the 21st century. Part of the apparent increase of VSLS in the tropical lower stratosphere results from an increase in the corresponding tropopause height. As the depletion of stratospheric ozone due to bromine depends also on the availability of chlorine, we find the impact of bromine on stratospheric ozone at the end of the 21st century reduced compared to present day. Thus, these studies highlight the different factors influencing the role of brominated VSLS in a future climate.

scholarly journals Laboratory evaluation of the effect of nitric acid uptake on frost point hygrometer performance

2011 ◽  
Vol 4 (2) ◽  
pp. 289-296 ◽  
Author(s):  
T. Thornberry ◽  
T. Gierczak ◽  
R. S. Gao ◽  
H. Vömel ◽  
L. A. Watts ◽  
...  
Keyword(s):  
Nitric Acid ◽  
Surface Area ◽  
Water Vapour ◽  
Lower Stratosphere ◽  
Laboratory Evaluation ◽  
Acid Uptake ◽  
Reliable Determination ◽  
Point Temperature ◽  
Mixing Ratios ◽  
Frost Point

Abstract. Chilled mirror hygrometers (CMH) are widely used to measure water vapour in the troposphere and lower stratosphere from balloon-borne sondes. Systematic discrepancies among in situ water vapour instruments have been observed at low water vapour mixing ratios (<5 ppm) in the upper troposphere and lower stratosphere (UT/LS). Understanding the source of the measurement discrepancies is important for a more accurate and reliable determination of water vapour abundance in this region. We have conducted a laboratory study to investigate the potential interference of gas-phase nitric acid (HNO3) with the measurement of frost point temperature, and consequently the water vapour mixing ratio, determined by CMH under conditions representative of operation in the UT/LS. No detectable interference in the measured frost point temperature was found for HNO3 mixing ratios of up to 4 ppb for exposure times up to 150 min. HNO3 was observed to co-condense on the mirror frost, with the adsorbed mass increasing linearly with time at constant exposure levels. Over the duration of a typical balloon sonde ascent (90–120 min), the maximum accumulated HNO3 amounts were comparable to monolayer coverage of the geometric mirror surface area, which corresponds to only a small fraction of the actual frost layer surface area. This small amount of co-condensed HNO3 is consistent with the observed lack of HNO3 interference in the frost point measurement because the CMH utilizes significant reductions (>10%) in surface reflectivity by the condensate to determine H2O.

scholarly journals Stratospheric water vapour budget and convection overshooting the tropopause: modelling study from SCOUT-AMMA

2010 ◽  
Vol 10 (17) ◽  
pp. 8267-8286 ◽  
Author(s):  
X. M. Liu ◽  
E. D. Rivière ◽  
V. Marécal ◽  
G. Durry ◽  
A. Hamdouni ◽  
...  
Keyword(s):  
Brightness Temperature ◽  
Water Vapour ◽  
Temperature Difference ◽  
Water Distribution ◽  
Lower Stratosphere ◽  
Background Level ◽  
Convective System ◽  
Regional Atmospheric Modelling System ◽  
Initial Location ◽  
The Impact

Abstract. The aim of this paper is to study the impacts of overshooting convection at a local scale on the water distribution in the tropical UTLS. Overshooting convection is assumed to be one of the processes controlling the entry of water vapour mixing ratio in the stratosphere by injecting ice crystals above the tropopause which later sublimate and hydrate the lower stratosphere. For this purpose, we quantify the individual impact of two cases of overshooting convection in Africa observed during SCOUT-AMMA: the case of 4 August 2006 over Southern Chad which is likely to have influenced the water vapour measurements by micro-SDLA and FLASH-B from Niamey on 5 August, and the case of a mesoscale convective system over Aïr on 5 August 2006. We make use of high resolution (down to 1 km horizontally) nested grid simulations with the three-dimensional regional atmospheric model BRAMS (Brazilian Regional Atmospheric Modelling System). In both cases, BRAMS succeeds in simulating the main features of the convective activity, as well as overshooting convection, though the exact position and time of the overshoots indicated by MSG brightness temperature difference is not fully reproduced (typically 1° displacement in latitude compared with the overshoots indicated by brightness temperature difference from satellite observations for both cases, and several hours shift for the Aïr case on 5 August 2006). Total water budgets associated with these two events show a significant injection of ice particles above the tropopause with maximum values of about 3.7 ton s−1 for the Chad case (4 August) and 1.4 ton s−1 for the Aïr case (5 August), and a total upward cross tropopause transport of about 3300 ton h−1 for the Chad case and 2400 ton h−1 for the Aïr case in the third domain of simulation. The order of magnitude of these modelled fluxes is lower but comparable with similar studies in other tropical areas based on models. These two estimations exhibit significant differences and highlight variability among the cases of the impact of overshooting convection in hydrating the lower stratosphere. We show that the regional enhancement of water above the tropopause is between 0.21 to 0.67 ppmv between 380 and 400 K, generally in the range of other model estimations. The amount of water which remains in the stratosphere after the overshoot is estimated for both cases. A range of 330 to 507 tons is found for the Chad case and an upper limit of 200 tons is found for the Aïr case. Finally we emphasize that the hydrated area in the LS by overshooting convection can be advected relatively far away from the overshoot initial location, with locally mixing ratios of more than 3 ppmv higher than the background level, which is compatible with the balloon borne measurements performed above Niamey in the same air mass, 30 h after the overshoot.

scholarly journals Evaluation of balloon and satellite water vapour measurements in the Southern tropical and subtropical UTLS during the HIBISCUS campaign

2009 ◽  
Vol 9 (14) ◽  
pp. 5299-5319 ◽  
Author(s):  
N. Montoux ◽  
A. Hauchecorne ◽  
J.-P. Pommereau ◽  
F. Lefèvre ◽  
G. Durry ◽  
...  
Keyword(s):  
Water Vapour ◽  
Lower Stratosphere ◽  
Tunable Diode Laser ◽  
Absorption Bands ◽  
Upper Troposphere ◽  
Mixing Ratios ◽  
Water Vapour Concentration ◽  
Vapour Concentration ◽  
Remote Measurements

Abstract. Balloon water vapour in situ and remote measurements in the tropical upper troposphere and lower stratosphere (UTLS) obtained during the HIBISCUS campaign around 20° S in Brazil in February–March 2004 using a tunable diode laser (μSDLA), a surface acoustic wave (SAW) and a Vis-NIR solar occultation spectrometer (SAOZ) on a long duration balloon, have been used for evaluating the performances of satellite borne remote water vapour instruments available at the same latitude and measurement period. In the stratosphere, HALOE displays the best precision (2.5%), followed by SAGE II (7%), MIPAS (10%), SAOZ (20–25%) and SCIAMACHY (35%), all of which show approximately constant H2O mixing ratios between 20–25 km. Compared to HALOE of ±10% accuracy between 0.1–100 hPa, SAGE II and SAOZ show insignificant biases, MIPAS is wetter by 10% and SCIAMACHY dryer by 20%. The currently available GOMOS profiles of 25% precision show a positive vertical gradient in error for identified reasons. Compared to these, the water vapour of the Reprobus Chemistry Transport Model, forced at pressures higher than 95 hPa by the ECMWF analyses, is dryer by about 1 ppmv (20%). In the lower stratosphere between 16–20 km, most notable features are the steep degradation of MIPAS precision below 18 km, and the appearance of biases between instruments far larger than their quoted total uncertainty. HALOE and SAGE II (after spectral adjustment for reducing the bias with HALOE at northern mid-latitudes) both show decreases of water vapour with a minimum at the tropopause not seen by other instruments or the model, possibly attributable to an increasing error in the HALOE altitude registration. Between 16–18 km where the water vapour concentration shows little horizontal variability, and where the μSDLA balloon measurements are not perturbed by outgassing, the average mixing ratios reported by the remote sensing instruments are substantially lower than the 4–5 ppmv observed by the μSDLA. Differences between μSDLA and HALOE and SAGE II (of the order of −2 ppmv), SCIAMACHY, MIPAS and GOMOS (−1 ppmv) and SAOZ (−0.5 ppmv), exceed the 10% uncertainty of μSDLA, implying larger systematic errors than estimated for the various instruments. In the upper troposphere, where the water vapour concentration is highly variable, AIRS v5 appears to be the most consistent within its 25% uncertainty with balloon in-situ measurements as well as ECMWF. Most of the remote measurements show less reliability in the upper troposphere, losing sensitivity possibly because of absorption line saturation in their spectral ranges (HALOE, SAGE II and SCIAMACHY), instrument noise exceeding 100% (MIPAS) or imperfect refraction correction (GOMOS). An exception is the SAOZ-balloon, employing smaller H2O absorption bands in the troposphere.

scholarly journals Airborne measurements of HCl from the marine boundary layer to the lower stratosphere over the North Pacific Ocean during INTEX-B

2008 ◽  
Vol 8 (1) ◽  
pp. 3563-3595 ◽  
Author(s):  
S. Kim ◽  
L. G. Huey ◽  
R. E. Stickel ◽  
R. B. Pierce ◽  
G. Chen ◽  
...  
Keyword(s):  
Boundary Layer ◽  
Lower Stratosphere ◽  
Marine Boundary Layer ◽  
North Pacific Ocean ◽  
Stratospheric Ozone ◽  
Background Level ◽  
Upper Troposphere ◽  
Airborne Measurements ◽  
The North ◽  
The Impact

Abstract. Gas phase HCl was measured from the marine boundary layer (MBL) to the lower stratosphere from the NASA DC-8 during five science flights (41 h) of the Intercontinental Chemical Transport Experiment-Phase B (INTEX-B) field campaign. In the upper troposphere/lower stratosphere (UT/LS, 8–12 km) HCl was observed to range from a few tens to 100 pptv due to stratospheric influence with a background tropospheric level of less than 2 pptv. In the 8–12 km altitude range, a simple analysis of the O3/HCl correlation shows that pure stratospheric and mixed tropospheric/stratospheric air masses were encountered 30% and 15% of the time, respectively. In the mid troposphere (4–8 km) HCl levels were usually below 2 pptv except for a few cases of stratospheric influence and were much lower than reported in previous work. These data indicate that background levels of HCl in the mid and upper troposphere are very low and confirm its use in these regions as a tracer of stratospheric ozone. However, a case study suggests that HCl may be produced in the mid troposphere by the dechlorination of dust aerosols. In the remote marine boundary layer HCl levels were consistently above 20 pptv (up to 140 pptv) and strongly correlated with HNO3. Cl atom levels were estimated from the background level of HCl in the MBL. This analysis suggests a Cl concentration of ~3×103 atoms cm−3, which corresponds to the lower range of previous studies. Finally, the observed HCl levels are compared to predictions by the Real-time Air Quality Modeling System (RAQMS) to assess its ability to characterize the impact of stratospheric transport on the upper troposphere.

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