Articles | Volume 15, issue 12
https://doi.org/10.5194/acp-15-6651-2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
https://doi.org/10.5194/acp-15-6651-2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Research article
| 
16 Jun 2015
Research article |
| 16 Jun 2015
Lagrangian analysis of microphysical and chemical processes in the Antarctic stratosphere: a case study
L. Di Liberto
Institute for Atmospheric Sciences and Climate, ISAC-CNR, Rome, Italy
R. Lehmann
Alfred Wegener Institute, Potsdam, Germany
I. Tritscher
Institute for Atmospheric and Climate Science, ETH Zurich, Zurich, Switzerland
Institut für Energie und Klimaforschung - Stratosphäre (IEK-7), Forschungszentrum Jülich, Jülich, Germany
F. Fierli
Institute for Atmospheric Sciences and Climate, ISAC-CNR, Rome, Italy
J. L. Mercer
Department of Atmospheric Science, University of Wyoming, Laramie, Wyoming, USA
Institute for Atmospheric Sciences and Climate, ISAC-CNR, Rome, Italy
G. Di Donfrancesco
Ente per le Nuove Tecnologie Energia e Ambiente, Santa Maria di Galeria, Rome, Italy
T. Deshler
Department of Atmospheric Science, University of Wyoming, Laramie, Wyoming, USA
B. P. Luo
Institute for Atmospheric and Climate Science, ETH Zurich, Zurich, Switzerland
J-U. Grooß
Institut für Energie und Klimaforschung - Stratosphäre (IEK-7), Forschungszentrum Jülich, Jülich, Germany
E. Arnone
Institute for Atmospheric Sciences and Climate, ISAC-CNR, Rome, Italy
B. M. Dinelli
Institute for Atmospheric Sciences and Climate, ISAC-CNR, Rome, Italy
Institute for Atmospheric Sciences and Climate, ISAC-CNR, Rome, Italy
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William G. Read, Gabriele Stiller, Stefan Lossow, Michael Kiefer, Farahnaz Khosrawi, Dale Hurst, Holger Vömel, Karen Rosenlof, Bianca M. Dinelli, Piera Raspollini, Gerald E. Nedoluha, John C. Gille, Yasuko Kasai, Patrick Eriksson, Christopher E. Sioris, Kaley A. Walker, Katja Weigel, John P. Burrows, and Alexei Rozanov
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Piera Raspollini, Enrico Arnone, Flavio Barbara, Massimo Bianchini, Bruno Carli, Simone Ceccherini, Martyn P. Chipperfield, Angelika Dehn, Stefano Della Fera, Bianca Maria Dinelli, Anu Dudhia, Jean-Marie Flaud, Marco Gai, Michael Kiefer, Manuel López-Puertas, David P. Moore, Alessandro Piro, John J. Remedios, Marco Ridolfi, Harjinder Sembhi, Luca Sgheri, and Nicola Zoppetti
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Sergey M. Khaykin, Elizabeth Moyer, Martina Krämer, Benjamin Clouser, Silvia Bucci, Bernard Legras, Alexey Lykov, Armin Afchine, Francesco Cairo, Ivan Formanyuk, Valentin Mitev, Renaud Matthey, Christian Rolf, Clare E. Singer, Nicole Spelten, Vasiliy Volkov, Vladimir Yushkov, and Fred Stroh
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Francesco Cairo, Terry Deshler, Luca Di Liberto, Andrea Scoccione, and Marcel Snels
Atmos. Meas. Tech. Discuss., https://doi.org/10.5194/amt-2022-28, https://doi.org/10.5194/amt-2022-28, 2022
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We study Mie theory on aspherical scatterers, computing on coincident measurements of PSC by lidar and Particle Counters, the backscatter and depolarization of mixed phase PSC. WParticles are assumed solid if larger than R; for these, Mie results are reduced by C < 1 and only a common fraction X < 1 of the backscattering is polarized. We retrieve R, C and X. The match of model and measurement is good for backscattering, poor for depolarization. The hypothesis on X may be not fulfilled.
Bianca Maria Dinelli, Piera Raspollini, Marco Gai, Luca Sgheri, Marco Ridolfi, Simone Ceccherini, Flavio Barbara, Nicola Zoppetti, Elisa Castelli, Enzo Papandrea, Paolo Pettinari, Angelika Dehn, Anu Dudhia, Michael Kiefer, Alessandro Piro, Jean-Marie Flaud, Manuel López-Puertas, David Moore, John Remedios, and Massimo Bianchini
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Marcel Snels, Stefania Stefani, Angelo Boccaccini, David Biondi, and Giuseppe Piccioni
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A novel simulation chamber, PASSxS (Planetary Atmosphere Simulation System for Spectroscopy), has been developed for absorption measurements with a Fourier transform spectrometer (FTS) and possibly a cavity ring-down (CRD) spectrometer, with a sample temperature ranging from 100 K up to 550 K, while the pressure of the gas can be varied up to 60 bar. These temperature and pressure ranges cover a significant part of the planetary atmospheres in the solar system and possibly extrasolar planets.
Christoph Mahnke, Ralf Weigel, Francesco Cairo, Jean-Paul Vernier, Armin Afchine, Martina Krämer, Valentin Mitev, Renaud Matthey, Silvia Viciani, Francesco D'Amato, Felix Ploeger, Terry Deshler, and Stephan Borrmann
Atmos. Chem. Phys., 21, 15259–15282, https://doi.org/10.5194/acp-21-15259-2021, https://doi.org/10.5194/acp-21-15259-2021, 2021
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In 2017, in situ aerosol measurements were conducted aboard the M55 Geophysica in the Asian monsoon region. The vertical particle mixing ratio profiles show a distinct layer (15–18.5 km), the Asian tropopause aerosol layer (ATAL). The backscatter ratio (BR) was calculated based on the aerosol size distributions and compared with the BRs detected by a backscatter probe and a lidar aboard M55, and by the CALIOP lidar. All four methods show enhanced BRs in the ATAL altitude range (max. at 17.5 km).
Ralf Weigel, Christoph Mahnke, Manuel Baumgartner, Antonis Dragoneas, Bärbel Vogel, Felix Ploeger, Silvia Viciani, Francesco D'Amato, Silvia Bucci, Bernard Legras, Beiping Luo, and Stephan Borrmann
Atmos. Chem. Phys., 21, 11689–11722, https://doi.org/10.5194/acp-21-11689-2021, https://doi.org/10.5194/acp-21-11689-2021, 2021
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In July and August 2017, eight StratoClim mission flights of the Geophysica reached up to 20 km in the Asian monsoon anticyclone. New particle formation (NPF) was identified in situ by abundant nucleation-mode aerosols (6–15 nm in diameter) with mixing ratios of up to 50 000 mg−1. NPF occurred most frequently at 12–16 km with fractions of non-volatile residues of down to 15 %. Abundance and productivity of observed NPF indicate its ability to promote the Asian tropopause aerosol layer.
Michael Weimer, Jennifer Buchmüller, Lars Hoffmann, Ole Kirner, Beiping Luo, Roland Ruhnke, Michael Steiner, Ines Tritscher, and Peter Braesicke
Atmos. Chem. Phys., 21, 9515–9543, https://doi.org/10.5194/acp-21-9515-2021, https://doi.org/10.5194/acp-21-9515-2021, 2021
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We show that we are able to directly simulate polar stratospheric clouds formed locally in a mountain wave and represent their effect on the ozone chemistry with the global atmospheric chemistry model ICON-ART. Thus, we show the first simulations that close the gap between directly resolved mountain-wave-induced polar stratospheric clouds and their representation at coarse global resolutions.
Francesco Cairo, Mauro De Muro, Marcel Snels, Luca Di Liberto, Silvia Bucci, Bernard Legras, Ajil Kottayil, Andrea Scoccione, and Stefano Ghisu
Atmos. Chem. Phys., 21, 7947–7961, https://doi.org/10.5194/acp-21-7947-2021, https://doi.org/10.5194/acp-21-7947-2021, 2021
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A lidar was used in Palau from February–March 2016. Clouds were observed peaking at 3 km below the high cold-point tropopause (CPT). Their occurrence was linked with cold anomalies, while in warm cases, cirrus clouds were restricted to 5 km below the CPT. Thin subvisible cirrus (SVC) near the CPT had distinctive characteristics. They were linked to wave-induced cold anomalies. Back trajectories are mostly compatible with convective outflow, while some distinctive SVC may originate in situ.
Lars E. Kalnajs, Sean M. Davis, J. Douglas Goetz, Terry Deshler, Sergey Khaykin, Alex St. Clair, Albert Hertzog, Jerome Bordereau, and Alexey Lykov
Atmos. Meas. Tech., 14, 2635–2648, https://doi.org/10.5194/amt-14-2635-2021, https://doi.org/10.5194/amt-14-2635-2021, 2021
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This work introduces a novel instrument system for high-resolution atmospheric profiling, which lowers and retracts a suspended instrument package beneath drifting long-duration balloons. During a 100 d circumtropical flight, the instrument collected over a hundred 2 km profiles of temperature, water vapor, clouds, and aerosol at 1 m resolution, yielding unprecedented geographic sampling and vertical resolution measurements of the tropical tropopause layer.
Marcel Snels, Francesco Colao, Francesco Cairo, Ilir Shuli, Andrea Scoccione, Mauro De Muro, Michael Pitts, Lamont Poole, and Luca Di Liberto
Atmos. Chem. Phys., 21, 2165–2178, https://doi.org/10.5194/acp-21-2165-2021, https://doi.org/10.5194/acp-21-2165-2021, 2021
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A total of 5 years of polar stratospheric cloud (PSC) observations by ground-based lidar at Concordia station (Antarctica) are presented. These data have been recorded in coincidence with the overpasses of the CALIOP lidar on the CALIPSO satellite. First we demonstrate that both lidars observe essentially the same thing, in terms of detection and composition of the PSCs. Then we use both datasets to study seasonal and interannual variations in the formation temperature of NAT mixtures.
Michael Steiner, Beiping Luo, Thomas Peter, Michael C. Pitts, and Andrea Stenke
Geosci. Model Dev., 14, 935–959, https://doi.org/10.5194/gmd-14-935-2021, https://doi.org/10.5194/gmd-14-935-2021, 2021
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We evaluate polar stratospheric clouds (PSCs) as simulated by the chemistry–climate model (CCM) SOCOLv3.1 in comparison with measurements by the CALIPSO satellite. A cold bias results in an overestimated PSC area and mountain-wave ice is underestimated, but we find overall good temporal and spatial agreement of PSC occurrence and composition. This work confirms previous studies indicating that simplified PSC schemes may also achieve good approximations of the fundamental properties of PSCs.
Teresa Jorge, Simone Brunamonti, Yann Poltera, Frank G. Wienhold, Bei P. Luo, Peter Oelsner, Sreeharsha Hanumanthu, Bhupendra B. Singh, Susanne Körner, Ruud Dirksen, Manish Naja, Suvarna Fadnavis, and Thomas Peter
Atmos. Meas. Tech., 14, 239–268, https://doi.org/10.5194/amt-14-239-2021, https://doi.org/10.5194/amt-14-239-2021, 2021
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Balloon-borne frost point hygrometers are crucial for the monitoring of water vapour in the upper troposphere and lower stratosphere. We found that when traversing a mixed-phase cloud with big supercooled droplets, the intake tube of the instrument collects on its inner surface a high percentage of these droplets. The newly formed ice layer will sublimate at higher levels and contaminate the measurement. The balloon is also a source of contamination, but only at higher levels during the ascent.
Jing Dou, Peter A. Alpert, Pablo Corral Arroyo, Beiping Luo, Frederic Schneider, Jacinta Xto, Thomas Huthwelker, Camelia N. Borca, Katja D. Henzler, Jörg Raabe, Benjamin Watts, Hartmut Herrmann, Thomas Peter, Markus Ammann, and Ulrich K. Krieger
Atmos. Chem. Phys., 21, 315–338, https://doi.org/10.5194/acp-21-315-2021, https://doi.org/10.5194/acp-21-315-2021, 2021
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Photochemistry of iron(III) complexes plays an important role in aerosol aging, especially in the lower troposphere. Ensuing radical chemistry leads to decarboxylation, and the production of peroxides, and oxygenated volatile compounds, resulting in particle mass loss due to release of the volatile products to the gas phase. We investigated kinetic transport limitations due to high particle viscosity under low relative humidity conditions. For quantification a numerical model was developed.
Sreeharsha Hanumanthu, Bärbel Vogel, Rolf Müller, Simone Brunamonti, Suvarna Fadnavis, Dan Li, Peter Ölsner, Manish Naja, Bhupendra Bahadur Singh, Kunchala Ravi Kumar, Sunil Sonbawne, Hannu Jauhiainen, Holger Vömel, Beiping Luo, Teresa Jorge, Frank G. Wienhold, Ruud Dirkson, and Thomas Peter
Atmos. Chem. Phys., 20, 14273–14302, https://doi.org/10.5194/acp-20-14273-2020, https://doi.org/10.5194/acp-20-14273-2020, 2020
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During boreal summer, anthropogenic sources yield the Asian Tropopause Aerosol Layer (ATAL), found in Asia between about 13 and 18 km altitude. Balloon-borne measurements of the ATAL conducted in northern India in 2016 show the strong variability of the ATAL. To explain its observed variability, model simulations are performed to deduce the origin of air masses on the Earth's surface, which is important to develop recommendations for regulations of anthropogenic surface emissions of the ATAL.
Joram J. D. Hooghiem, Maria Elena Popa, Thomas Röckmann, Jens-Uwe Grooß, Ines Tritscher, Rolf Müller, Rigel Kivi, and Huilin Chen
Atmos. Chem. Phys., 20, 13985–14003, https://doi.org/10.5194/acp-20-13985-2020, https://doi.org/10.5194/acp-20-13985-2020, 2020
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Wildfires release a large quantity of pollutants that can reach the stratosphere through pyro-convection events. In September 2017, a stratospheric plume was accidentally sampled during balloon soundings in northern Finland. The source of the plume was identified to be wildfire smoke based on in situ measurements of carbon monoxide (CO) and stable isotope analysis of CO. Furthermore, the age of the plume was estimated using backwards transport modelling to be ~24 d, with its origin in Canada.
Silvia Bucci, Bernard Legras, Pasquale Sellitto, Francesco D'Amato, Silvia Viciani, Alessio Montori, Antonio Chiarugi, Fabrizio Ravegnani, Alexey Ulanovsky, Francesco Cairo, and Fred Stroh
Atmos. Chem. Phys., 20, 12193–12210, https://doi.org/10.5194/acp-20-12193-2020, https://doi.org/10.5194/acp-20-12193-2020, 2020
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The paper presents and evaluates a transport analysis method to study the convective injection of air in the upper troposphere–lower stratosphere of the Asian monsoon anticyclone region. The approach is thereby used to analyse the trace gas data collected during the StratoClim aircraft campaign. The results showed that fresh convective air can be injected fast at a high level of the atmosphere (above 17 km), with potential impacts on the stratospheric chemistry of the Northern Hemisphere.
Ernest Nyaku, Robert Loughman, Pawan K. Bhartia, Terry Deshler, Zhong Chen, and Peter R. Colarco
Atmos. Meas. Tech., 13, 1071–1087, https://doi.org/10.5194/amt-13-1071-2020, https://doi.org/10.5194/amt-13-1071-2020, 2020
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This paper shows the importance of the nature of the aerosol phase function used in the retrieval of the stratospheric aerosol extinction from limb scattering measurements. The aerosol phase function is derived from the parameters using either a unimodal lognormal or gamma aerosol size distribution. These two distributions were fitted to the same aerosol concentration measurements at two altitudes, and depending on the nature of the measurements, each distribution shows its strengths.
Enzo Papandrea, Stefano Casadio, Elisa Castelli, Bianca Maria Dinelli, and Mario Marcello Miglietta
Atmos. Meas. Tech., 12, 6683–6693, https://doi.org/10.5194/amt-12-6683-2019, https://doi.org/10.5194/amt-12-6683-2019, 2019
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Lee waves have been detected in clear-sky conditions over the Mediterranean Sea using the total column water vapour (TCWV) fields. The products were generated applying the Advanced Infra-Red WAter Vapour Estimator (AIRWAVE) retrieval algorithm to the thermal infrared measurements of the Along Track Scanning Radiometer (ATSR) instrument series. A subset of the occurrences has been compared with both independent observations and model simulations.
Ingo Wohltmann, Ralph Lehmann, Georg A. Gottwald, Karsten Peters, Alain Protat, Valentin Louf, Christopher Williams, Wuhu Feng, and Markus Rex
Geosci. Model Dev., 12, 4387–4407, https://doi.org/10.5194/gmd-12-4387-2019, https://doi.org/10.5194/gmd-12-4387-2019, 2019
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We present a trajectory-based model for simulating the transport of air parcels by convection. Our model extends the approach of existing models by explicitly simulating vertical updraft velocities inside the clouds and the time that an air parcel spends inside the convective event.
Aryeh Feinberg, Timofei Sukhodolov, Bei-Ping Luo, Eugene Rozanov, Lenny H. E. Winkel, Thomas Peter, and Andrea Stenke
Geosci. Model Dev., 12, 3863–3887, https://doi.org/10.5194/gmd-12-3863-2019, https://doi.org/10.5194/gmd-12-3863-2019, 2019
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We have improved several aspects of atmospheric sulfur cycling in SOCOL-AER, an aerosol–chemistry–climate model. The newly implemented features in SOCOL-AERv2 include interactive deposition schemes, improved sulfur mass conservation, and expanded tropospheric chemistry. SOCOL-AERv2 shows better agreement with stratospheric aerosol observations and sulfur deposition networks compared to SOCOL-AERv1. SOCOL-AERv2 can be used to study impacts of sulfate aerosol on climate, chemistry, and ecosystems.
Sören Johansson, Michelle L. Santee, Jens-Uwe Grooß, Michael Höpfner, Marleen Braun, Felix Friedl-Vallon, Farahnaz Khosrawi, Oliver Kirner, Erik Kretschmer, Hermann Oelhaf, Johannes Orphal, Björn-Martin Sinnhuber, Ines Tritscher, Jörn Ungermann, Kaley A. Walker, and Wolfgang Woiwode
Atmos. Chem. Phys., 19, 8311–8338, https://doi.org/10.5194/acp-19-8311-2019, https://doi.org/10.5194/acp-19-8311-2019, 2019
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We present a study based on GLORIA aircraft and MLS/ACE-FTS/CALIOP satellite measurements during the Arctic winter 2015/16, which demonstrate (for the Arctic) unusual chlorine deactivation into HCl instead of ClONO2 due to low ozone abundances in the lowermost stratosphere, with a focus at 380 K potential temperature. The atmospheric models CLaMS and EMAC are evaluated, and measured ClONO2 is linked with transport and in situ deactivation in the lowermost stratosphere.
Stefan Lossow, Farahnaz Khosrawi, Michael Kiefer, Kaley A. Walker, Jean-Loup Bertaux, Laurent Blanot, James M. Russell, Ellis E. Remsberg, John C. Gille, Takafumi Sugita, Christopher E. Sioris, Bianca M. Dinelli, Enzo Papandrea, Piera Raspollini, Maya García-Comas, Gabriele P. Stiller, Thomas von Clarmann, Anu Dudhia, William G. Read, Gerald E. Nedoluha, Robert P. Damadeo, Joseph M. Zawodny, Katja Weigel, Alexei Rozanov, Faiza Azam, Klaus Bramstedt, Stefan Noël, John P. Burrows, Hideo Sagawa, Yasuko Kasai, Joachim Urban, Patrick Eriksson, Donal P. Murtagh, Mark E. Hervig, Charlotta Högberg, Dale F. Hurst, and Karen H. Rosenlof
Atmos. Meas. Tech., 12, 2693–2732, https://doi.org/10.5194/amt-12-2693-2019, https://doi.org/10.5194/amt-12-2693-2019, 2019
Marcel Snels, Andrea Scoccione, Luca Di Liberto, Francesco Colao, Michael Pitts, Lamont Poole, Terry Deshler, Francesco Cairo, Chiara Cagnazzo, and Federico Fierli
Atmos. Chem. Phys., 19, 955–972, https://doi.org/10.5194/acp-19-955-2019, https://doi.org/10.5194/acp-19-955-2019, 2019
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Polar stratospheric clouds are important for stratospheric chemistry and ozone depletion. Here we statistically compare ground-based and satellite-borne lidar measurements at McMurdo (Antarctica) in order to better understand the differences between ground-based and satellite-borne observations. The satellite observations have also been compared to models used in CCMVAL-2 and CCMI studies, with the goal of testing different diagnostic methods for comparing observations with model outputs.
Elisa Castelli, Enzo Papandrea, Alessio Di Roma, Bianca Maria Dinelli, Stefano Casadio, and Bojan Bojkov
Atmos. Meas. Tech., 12, 371–388, https://doi.org/10.5194/amt-12-371-2019, https://doi.org/10.5194/amt-12-371-2019, 2019
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The total column water vapour (TCWV) is a key atmospheric variable. The AIRWAVE (Advanced Infra-Red WAter Vapour Estimator) v1 algorithm was developed to retrieve TCWV from satellite measurements. Comparisons with independent TCWV show good agreement with an overall bias of 0.72 kg m−2 due to the polar and coastal regions. Here, we describe the AIRWAVEv2 dataset, which shows significant improvements with a global bias of 0.02 kg m−2. This dataset was used to produce a climatology from 1991 to 2012.
Ines Tritscher, Jens-Uwe Grooß, Reinhold Spang, Michael C. Pitts, Lamont R. Poole, Rolf Müller, and Martin Riese
Atmos. Chem. Phys., 19, 543–563, https://doi.org/10.5194/acp-19-543-2019, https://doi.org/10.5194/acp-19-543-2019, 2019
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We present Lagrangian simulations of polar stratospheric clouds (PSCs) for the Arctic winter 2009/2010 and the Antarctic winter 2011 using the Chemical Lagrangian Model of the Stratosphere (CLaMS). The paper comprises a detailed model description with ice PSCs and related dehydration being the focus of this study. Comparisons between our simulations and observations from different satellites on season-long and vortex-wide scales as well as for single PSC events show an overall good agreement.
Davide Dionisi, Francesca Barnaba, Henri Diémoz, Luca Di Liberto, and Gian Paolo Gobbi
Atmos. Meas. Tech., 11, 6013–6042, https://doi.org/10.5194/amt-11-6013-2018, https://doi.org/10.5194/amt-11-6013-2018, 2018
Simone Brunamonti, Teresa Jorge, Peter Oelsner, Sreeharsha Hanumanthu, Bhupendra B. Singh, K. Ravi Kumar, Sunil Sonbawne, Susanne Meier, Deepak Singh, Frank G. Wienhold, Bei Ping Luo, Maxi Boettcher, Yann Poltera, Hannu Jauhiainen, Rijan Kayastha, Jagadishwor Karmacharya, Ruud Dirksen, Manish Naja, Markus Rex, Suvarna Fadnavis, and Thomas Peter
Atmos. Chem. Phys., 18, 15937–15957, https://doi.org/10.5194/acp-18-15937-2018, https://doi.org/10.5194/acp-18-15937-2018, 2018
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Based on balloon-borne measurements performed in India and Nepal in 2016–2017, we infer the vertical distributions of water vapor, ozone and aerosols in the atmosphere, from the surface to 30 km altitude. Our measurements show that the atmospheric dynamics of the Asian summer monsoon system over the polluted Indian subcontinent lead to increased concentrations of water vapor and aerosols in the high atmosphere (approximately 14–20 km altitude), which can have an important effect on climate.
Michael Höpfner, Terry Deshler, Michael Pitts, Lamont Poole, Reinhold Spang, Gabriele Stiller, and Thomas von Clarmann
Atmos. Meas. Tech., 11, 5901–5923, https://doi.org/10.5194/amt-11-5901-2018, https://doi.org/10.5194/amt-11-5901-2018, 2018
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Polar stratospheric clouds (PSC) have major relevance to the processes leading to polar ozone depletion. A good understanding of these particles is a prerequisite to predict their role in a changing climate. We present the first global set of PSC volume density profiles derived from the MIPAS satellite measurements covering the entire mission period between 2002 and 2012. A comparison to CALIOP lidar measurements is provided. The dataset can serve as a basis for evaluation of atmospheric models.
Norbert Glatthor, Thomas von Clarmann, Gabriele P. Stiller, Michael Kiefer, Alexandra Laeng, Bianca M. Dinelli, Gerald Wetzel, and Johannes Orphal
Atmos. Meas. Tech., 11, 4707–4723, https://doi.org/10.5194/amt-11-4707-2018, https://doi.org/10.5194/amt-11-4707-2018, 2018
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We report differences in ozone retrievals in channels A and AB of the space-borne Michelson Interferometer for Passive Atmospheric Sounding (MIPAS), which amount to up to 8 %. We provide strong evidence that the bias is caused by inconsistencies in different spectroscopic databases (MIPAS, HITRAN, GEISA). We show that a major part of the differences can be attributed to inconsistent air-broadening coefficients of the ozone lines contained in the databases.
Timofei Sukhodolov, Jian-Xiong Sheng, Aryeh Feinberg, Bei-Ping Luo, Thomas Peter, Laura Revell, Andrea Stenke, Debra K. Weisenstein, and Eugene Rozanov
Geosci. Model Dev., 11, 2633–2647, https://doi.org/10.5194/gmd-11-2633-2018, https://doi.org/10.5194/gmd-11-2633-2018, 2018
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The Pinatubo eruption in 1991 is the strongest directly observed volcanic event. In a series of experiments, we simulate its influence on the stratospheric aerosol layer using a state-of-the-art aerosol–chemistry–climate model, SOCOL-AERv1.0, and compare our results to observations. We show that SOCOL-AER reproduces the most important atmospheric effects and can therefore be used to study the climate effects of future volcanic eruptions and geoengineering by artificial sulfate aerosol.
Jens-Uwe Grooß, Rolf Müller, Reinhold Spang, Ines Tritscher, Tobias Wegner, Martyn P. Chipperfield, Wuhu Feng, Douglas E. Kinnison, and Sasha Madronich
Atmos. Chem. Phys., 18, 8647–8666, https://doi.org/10.5194/acp-18-8647-2018, https://doi.org/10.5194/acp-18-8647-2018, 2018
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We investigate a discrepancy between model simulations and observations of HCl in the dark polar stratosphere. In early winter, the less-well-studied period of the onset of chlorine activation, observations show a much faster depletion of HCl than simulations of three models. This points to some unknown process that is currently not represented in the models. Various hypotheses for potential causes are investigated that partly reduce the discrepancy. The impact on polar ozone depletion is low.
Anand Kumar, Claudia Marcolli, Beiping Luo, and Thomas Peter
Atmos. Chem. Phys., 18, 7057–7079, https://doi.org/10.5194/acp-18-7057-2018, https://doi.org/10.5194/acp-18-7057-2018, 2018
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We have performed immersion freezing experiments with microcline (most active ice nucleation, IN, K-feldspar polymorph) and investigated the effect of ammonium and non-ammonium solutes on its IN efficiency. We report increased IN efficiency of microcline in dilute ammonia- or ammonium-containing solutions, which opens up a pathway for condensation freezing occurring at a warmer temperature than immersion freezing.
Silvia Bucci, Paolo Cristofanelli, Stefano Decesari, Angela Marinoni, Silvia Sandrini, Johannes Größ, Alfred Wiedensohler, Chiara F. Di Marco, Eiko Nemitz, Francesco Cairo, Luca Di Liberto, and Federico Fierli
Atmos. Chem. Phys., 18, 5371–5389, https://doi.org/10.5194/acp-18-5371-2018, https://doi.org/10.5194/acp-18-5371-2018, 2018
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This paper analyses some of the processes affecting PM levels over the Po Valley, one of the most polluted regions of Europe, during the 2012 summer campaigns. Under conditions of air transport from the Sahara, data show that desert dust can rapidly penetrate into the lower atmosphere, directly affecting the PM concentration at the ground. Processes of particles growth in high relative humidity and uplift of local soil particles, potentially affecting PM level, are also analysed.
Reinhold Spang, Lars Hoffmann, Rolf Müller, Jens-Uwe Grooß, Ines Tritscher, Michael Höpfner, Michael Pitts, Andrew Orr, and Martin Riese
Atmos. Chem. Phys., 18, 5089–5113, https://doi.org/10.5194/acp-18-5089-2018, https://doi.org/10.5194/acp-18-5089-2018, 2018
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This paper represents an unprecedented pole-covering day- and nighttime climatology of the polar stratospheric clouds (PSCs) based on satellite measurements, their spatial distribution, and composition of different particle types. The climatology has a high potential for the validation and improvement of PSC schemes in chemical transport and chemistry–climate models, which is important for a better prediction of future polar ozone loss in a changing climate.
Larry W. Thomason, Nicholas Ernest, Luis Millán, Landon Rieger, Adam Bourassa, Jean-Paul Vernier, Gloria Manney, Beiping Luo, Florian Arfeuille, and Thomas Peter
Earth Syst. Sci. Data, 10, 469–492, https://doi.org/10.5194/essd-10-469-2018, https://doi.org/10.5194/essd-10-469-2018, 2018
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We describe the construction of a continuous 38-year record of stratospheric aerosol optical properties. The Global Space-based Stratospheric Aerosol Climatology, or GloSSAC, provided the input data to the construction of the Climate Model Intercomparison Project stratospheric aerosol forcing data set (1979 to 2014) and is now extended through 2016. GloSSAC focuses on the the SAGE series of instruments through mid-2005 and on OSIRIS and CALIPSO after that time.
Daniel Kreyling, Ingo Wohltmann, Ralph Lehmann, and Markus Rex
Geosci. Model Dev., 11, 753–769, https://doi.org/10.5194/gmd-11-753-2018, https://doi.org/10.5194/gmd-11-753-2018, 2018
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The Extrapolar SWIFT model is a fast yet accurate stratospheric ozone chemistry module for global climate models. The importance of feedbacks between the climate system and the ozone layer has been demonstrated in previous studies. Therefore it is desirable to include an interactive ozone layer in climate simulations. However, ensemble simulations in particular have strict computational constraints. The Extrapolar SWIFT model provides an interactive ozone layer with small computational costs.
Rolf Müller, Jens-Uwe Grooß, Abdul Mannan Zafar, Sabine Robrecht, and Ralph Lehmann
Atmos. Chem. Phys., 18, 2985–2997, https://doi.org/10.5194/acp-18-2985-2018, https://doi.org/10.5194/acp-18-2985-2018, 2018
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This paper revisits the chemistry leading to strong ozone depletion in the Antarctic. We focus on the heart of the ozone layer in the lowermost stratosphere in the core of the vortex. We argue that chemical cycles (referred to as HCl null cycles) that have hitherto been largely neglected counteract the deactivation of chlorine and are therefore key to ozone depletion in the core of the Antarctic vortex. The key process to full activation of chlorine is the photolysis of formaldehyde.
Annika Günther, Michael Höpfner, Björn-Martin Sinnhuber, Sabine Griessbach, Terry Deshler, Thomas von Clarmann, and Gabriele Stiller
Atmos. Chem. Phys., 18, 1217–1239, https://doi.org/10.5194/acp-18-1217-2018, https://doi.org/10.5194/acp-18-1217-2018, 2018
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Satellite-borne data of sulfur dioxide and a new data set of sulfate aerosol volume densities, as retrieved from MIPAS measurements, are studied in the upper-troposphere–lower-stratosphere region. General patterns of enhanced aerosol are in agreement with SO2. Via chemical transport model simulations for two volcanic eruptions in the Northern Hemisphere midlatitudes, we show that the volcanic enhancements in MIPAS SO2 and sulfate aerosol are consistent in terms of mass and transport patterns.
Gerald E. Nedoluha, Michael Kiefer, Stefan Lossow, R. Michael Gomez, Niklaus Kämpfer, Martin Lainer, Peter Forkman, Ole Martin Christensen, Jung Jin Oh, Paul Hartogh, John Anderson, Klaus Bramstedt, Bianca M. Dinelli, Maya Garcia-Comas, Mark Hervig, Donal Murtagh, Piera Raspollini, William G. Read, Karen Rosenlof, Gabriele P. Stiller, and Kaley A. Walker
Atmos. Chem. Phys., 17, 14543–14558, https://doi.org/10.5194/acp-17-14543-2017, https://doi.org/10.5194/acp-17-14543-2017, 2017
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As part of the second SPARC (Stratosphere–troposphere Processes And their Role in Climate) water vapor assessment (WAVAS-II), we present measurements taken from or coincident with seven sites from which ground-based microwave instruments measure water vapor in the middle atmosphere. In the lower mesosphere, we quantify instrumental differences in the observed trends and annual variations at six sites. We then present a range of observed trends in water vapor over the past 20 years.
Laura E. Revell, Andrea Stenke, Beiping Luo, Stefanie Kremser, Eugene Rozanov, Timofei Sukhodolov, and Thomas Peter
Atmos. Chem. Phys., 17, 13139–13150, https://doi.org/10.5194/acp-17-13139-2017, https://doi.org/10.5194/acp-17-13139-2017, 2017
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Compiling stratospheric aerosol data sets after a major volcanic eruption is difficult as the stratosphere becomes too optically opaque for satellite instruments to measure accurately. We performed ensemble chemistry–climate model simulations with two stratospheric aerosol data sets compiled for two international modelling activities and compared the simulated volcanic aerosol-induced effects from the 1991 Mt Pinatubo eruption on tropical stratospheric temperature and ozone with observations.
Gabriele P. Stiller, Federico Fierli, Felix Ploeger, Chiara Cagnazzo, Bernd Funke, Florian J. Haenel, Thomas Reddmann, Martin Riese, and Thomas von Clarmann
Atmos. Chem. Phys., 17, 11177–11192, https://doi.org/10.5194/acp-17-11177-2017, https://doi.org/10.5194/acp-17-11177-2017, 2017
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The discrepancy between modelled and observed 25-year trends of the strength of the stratospheric Brewer–Dobson circulation (BDC) is still not resolved. With our paper we trace the observed hemispheric dipole structure of age of air trends back to natural variability in shorter-term (decadal) time frames. Beyond this we demonstrate that after correction for the decadal natural variability the remaining trend for the first decade of the 21st century is consistent with model simulations.
Ingo Wohltmann, Ralph Lehmann, and Markus Rex
Atmos. Chem. Phys., 17, 10535–10563, https://doi.org/10.5194/acp-17-10535-2017, https://doi.org/10.5194/acp-17-10535-2017, 2017
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We present a quantitative analysis of the chemical reactions involved in polar ozone depletion in the stratosphere, and of the relevant reaction pathways and cycles. We show time series of reaction rates averaged over the core of the polar vortex in winter and spring for all relevant reactions. An emphasis is put on the partitioning of the relevant chemical families (nitrogen, hydrogen, chlorine, bromine and odd oxygen) and activation and deactivation of chlorine.
Ingo Wohltmann, Ralph Lehmann, and Markus Rex
Geosci. Model Dev., 10, 2671–2689, https://doi.org/10.5194/gmd-10-2671-2017, https://doi.org/10.5194/gmd-10-2671-2017, 2017
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The Polar SWIFT model is a fast scheme for calculating the chemistry of stratospheric ozone depletion in polar winter. It is intended for use in global climate models (GCMs) and Earth system models (ESMs) to enable the simulation of mutual interactions between the ozone layer and climate.
Sandra Bastelberger, Ulrich K. Krieger, Beiping Luo, and Thomas Peter
Atmos. Chem. Phys., 17, 8453–8471, https://doi.org/10.5194/acp-17-8453-2017, https://doi.org/10.5194/acp-17-8453-2017, 2017
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We present quantitative condensed-phase diffusivity measurements of a volatile organic (tetraethylene glycol) in highly viscous single aerosol particles (aqueous sucrose). The condensed-phase diffusivity exhibits a strong temperature and humidity dependence. Our results suggest that diffusion limitations of volatile organics in highly viscous organic aerosol may severely impact gas–particle partitioning under cold and dry conditions.
Terry Deshler, Rene Stübi, Francis J. Schmidlin, Jennifer L. Mercer, Herman G. J. Smit, Bryan J. Johnson, Rigel Kivi, and Bruno Nardi
Atmos. Meas. Tech., 10, 2021–2043, https://doi.org/10.5194/amt-10-2021-2017, https://doi.org/10.5194/amt-10-2021-2017, 2017
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Ozonesondes, small balloon-borne instruments to measure ozone profiles, are used once and lost. Quality control is thus essential. From the mid-1990s to late 2000s differences in manufacturers' (Science Pump and ENSCI) recommended sensor solution concentrations, 1.0 % and 0.5 % potassium iodide, led to some confusion. This paper uses comparison measurements to derive transfer functions to homogenize the measurements made with non-standard combinations of instrument and sensor solution.
Alexandra Laeng, Thomas von Clarmann, Gabriele Stiller, Bianca Maria Dinelli, Anu Dudhia, Piera Raspollini, Norbert Glatthor, Udo Grabowski, Viktoria Sofieva, Lucien Froidevaux, Kaley A. Walker, and Claus Zehner
Atmos. Meas. Tech., 10, 1511–1518, https://doi.org/10.5194/amt-10-1511-2017, https://doi.org/10.5194/amt-10-1511-2017, 2017
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A MIPAS instrument was flown in 2002–2012 on the Envisat satellite and measured atmospheric composition. There exist four processors retrieving atmospheric profiles from MIPAS spectra. We performed a mathematically clean merging of 2007–2008 datasets of ozone from these four processors. The merged product was compared with ozone datasets from ACE-FTS and MLS instruments. The advantages and the shortcomings of this merged product are discussed.
Stefan Lossow, Farahnaz Khosrawi, Gerald E. Nedoluha, Faiza Azam, Klaus Bramstedt, John. P. Burrows, Bianca M. Dinelli, Patrick Eriksson, Patrick J. Espy, Maya García-Comas, John C. Gille, Michael Kiefer, Stefan Noël, Piera Raspollini, William G. Read, Karen H. Rosenlof, Alexei Rozanov, Christopher E. Sioris, Gabriele P. Stiller, Kaley A. Walker, and Katja Weigel
Atmos. Meas. Tech., 10, 1111–1137, https://doi.org/10.5194/amt-10-1111-2017, https://doi.org/10.5194/amt-10-1111-2017, 2017
Lukas Kaufmann, Claudia Marcolli, Beiping Luo, and Thomas Peter
Atmos. Chem. Phys., 17, 3525–3552, https://doi.org/10.5194/acp-17-3525-2017, https://doi.org/10.5194/acp-17-3525-2017, 2017
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To improve the understanding of heterogeneous ice nucleation, we have subjected different ice nuclei to repeated freezing cycles and evaluated the freezing temperatures with different parameterizations of classical nucleation theory. It was found that two fit parameters were necessary to describe the temperature dependence of the nucleation rate.
Francesca Costabile, Stefania Gilardoni, Francesca Barnaba, Antonio Di Ianni, Luca Di Liberto, Davide Dionisi, Maurizio Manigrasso, Marco Paglione, Vanes Poluzzi, Matteo Rinaldi, Maria Cristina Facchini, and Gian Paolo Gobbi
Atmos. Chem. Phys., 17, 313–326, https://doi.org/10.5194/acp-17-313-2017, https://doi.org/10.5194/acp-17-313-2017, 2017
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We investigate the particle size distribution and spectral optical properties of brown carbon (BrC) associated with the formation of secondary aerosol in the ambient atmosphere and relate these properties to major aerosol chemical components. We found that BrC occurs in particles in the droplet mode size range, enriched in ammonium nitrate and poor in black carbon (BC), with a strong dependance on the organic aerosol to BC ratio.
Massimo Carlotti, Bianca Maria Dinelli, Giada Innocenti, and Luca Palchetti
Atmos. Meas. Tech., 9, 5853–5867, https://doi.org/10.5194/amt-9-5853-2016, https://doi.org/10.5194/amt-9-5853-2016, 2016
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We introduce a strategy for the measurement of CO2 in the stratosphere. We use an orbiting limb sounder to measure both the thermal infrared (TIR) and far-infrared (FIR) atmospheric emissions. The rotational transitions of O2 in the FIR are exploited to derive the temperature and pressure fields that are needed to retrieve the CO2 from its spectrum in the TIR. The proposed experiment can determine two-dimensional distributions of the CO2 with precision of 1 ppm at altitudes between 10 and 50 km.
Elisa Castelli, Marco Ridolfi, Massimo Carlotti, Björn-Martin Sinnhuber, Oliver Kirner, Michael Kiefer, and Bianca Maria Dinelli
Atmos. Meas. Tech., 9, 5499–5508, https://doi.org/10.5194/amt-9-5499-2016, https://doi.org/10.5194/amt-9-5499-2016, 2016
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MIPAS is a satellite-borne limb emission sounder. The algorithm used to infer atmospheric composition from its measurements exploits the assumption that the atmosphere is horizontally homogeneous. This assumption can cause significant errors. We use synthetic observations to quantify these errors. Furthermore we show that the inclusion of any kind of horizontal variability model improves all the retrieval targets and that the two-dimensional approach implies the smallest errors.
Massimo Valeri, Massimo Carlotti, Jean-Marie Flaud, Piera Raspollini, Marco Ridolfi, and Bianca Maria Dinelli
Atmos. Meas. Tech., 9, 4655–4663, https://doi.org/10.5194/amt-9-4655-2016, https://doi.org/10.5194/amt-9-4655-2016, 2016
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Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) measurements have been analysed to measure the vertical distribution of phosgene (COCl2) in the UTLS using new spectroscopic data. To highlight its seasonal and latitudinal variability, MIPAS measurements of 2 days/month during 2008 have been analysed. The results show a strong latitudinal variability of COCl2 with the largest VMR values observed in the tropical regions. The seasonality is fairly low, apart from the polar regions.
Gerald E. Nedoluha, Brian J. Connor, Thomas Mooney, James W. Barrett, Alan Parrish, R. Michael Gomez, Ian Boyd, Douglas R. Allen, Michael Kotkamp, Stefanie Kremser, Terry Deshler, Paul Newman, and Michelle L. Santee
Atmos. Chem. Phys., 16, 10725–10734, https://doi.org/10.5194/acp-16-10725-2016, https://doi.org/10.5194/acp-16-10725-2016, 2016
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Chlorine monoxide (ClO) is central to the formation of the springtime Antarctic ozone hole since it is the catalytic agent in the most important ozone-depleting chemical cycle. We present 20 years of measurements of ClO from the Chlorine monOxide Experiment at Scott Base, Antarctica, and 12 years of measurements from the Aura Microwave Limb Sounder to show that the trends in ClO during the ozone hole season are consistent with changes in stratospheric chlorine observed elsewhere.
Claudia Di Biagio, Paola Formenti, Lionel Doppler, Cécile Gaimoz, Noel Grand, Gerard Ancellet, Jean-Luc Attié, Silvia Bucci, Philippe Dubuisson, Federico Fierli, Marc Mallet, and François Ravetta
Atmos. Chem. Phys., 16, 10591–10607, https://doi.org/10.5194/acp-16-10591-2016, https://doi.org/10.5194/acp-16-10591-2016, 2016
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Pollution aerosols strongly influence the composition of the Western Mediterranean, but at present little is known on their optical properties. Here, we report observations of pollution aerosols measured during the TRAQA airborne campaign in summer 2012. Data from this study indicate a large variability of the absorption for pollution particles. This variability strongly influences their direct radiative effect, with possible consequences on the hydrological cycle in this part of the basin.
Erika Kienast-Sjögren, Christian Rolf, Patric Seifert, Ulrich K. Krieger, Bei P. Luo, Martina Krämer, and Thomas Peter
Atmos. Chem. Phys., 16, 7605–7621, https://doi.org/10.5194/acp-16-7605-2016, https://doi.org/10.5194/acp-16-7605-2016, 2016
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We present a climatology of mid-latitude cirrus cloud properties based on 13 000 hours of automatically analyzed lidar measurements at three different sites. Jungfraujoch,
situated at 3580 m a.s.l., is found to be ideal to measure high and optically thin
cirrus. We use our retrieved optical properties together with a radiation model and
estimate the radiative forcing by mid-latitude cirrus.
All cirrus clouds detected here have a positive net radiative effect.
Ugo Cortesi, Samuele Del Bianco, Simone Ceccherini, Marco Gai, Bianca Maria Dinelli, Elisa Castelli, Hermann Oelhaf, Wolfgang Woiwode, Michael Höpfner, and Daniel Gerber
Atmos. Meas. Tech., 9, 2267–2289, https://doi.org/10.5194/amt-9-2267-2016, https://doi.org/10.5194/amt-9-2267-2016, 2016
Markus Hermann, Andreas Weigelt, Denise Assmann, Sascha Pfeifer, Thomas Müller, Thomas Conrath, Jens Voigtländer, Jost Heintzenberg, Alfred Wiedensohler, Bengt G. Martinsson, Terry Deshler, Carl A. M. Brenninkmeijer, and Andreas Zahn
Atmos. Meas. Tech., 9, 2179–2194, https://doi.org/10.5194/amt-9-2179-2016, https://doi.org/10.5194/amt-9-2179-2016, 2016
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Aerosol particles are an important component of the Earth's atmosphere. Here we describe the composition and characterization of a new optical particle size spectrometer (OPSS) for aircraft-borne measurements of the aerosol particle size distribution (how many particles there are with a certain size) in the 140–1050 nm size range. The OPSS was characterized throughout concerning its measurement capabilities (response, pressure dependence, coincidence) and validated versus balloon measurement.
Bernadette Rosati, Erik Herrmann, Silvia Bucci, Federico Fierli, Francesco Cairo, Martin Gysel, Ralf Tillmann, Johannes Größ, Gian Paolo Gobbi, Luca Di Liberto, Guido Di Donfrancesco, Alfred Wiedensohler, Ernest Weingartner, Annele Virtanen, Thomas F. Mentel, and Urs Baltensperger
Atmos. Chem. Phys., 16, 4539–4554, https://doi.org/10.5194/acp-16-4539-2016, https://doi.org/10.5194/acp-16-4539-2016, 2016
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We present vertical profiles of aerosol optical properties, which were explored within the planetary boundary layer in a case study in 2012 in the Po Valley region. A comparison of in situ measurements recorded aboard a Zeppelin NT and ground-based remote-sensing data was performed yielding good agreement. Additionally, the role of ambient relative humidity for the aerosol particles' optical properties was investigated.
Tobias Wegner, Michael C. Pitts, Lamont R. Poole, Ines Tritscher, Jens-Uwe Grooß, and Hideaki Nakajima
Atmos. Chem. Phys., 16, 4569–4577, https://doi.org/10.5194/acp-16-4569-2016, https://doi.org/10.5194/acp-16-4569-2016, 2016
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Satellite observations are used to constrain areas with large backscatter values areas inside the polar vortex. Surface area is derived from these observations and used in heterogeneous modeling. Satellite gas species observations show a decrease in HCl downwind of areas with large surface area density indicating heterogeneous processing inside these areas. This decrease can only be simulated if a realistic surface area is assumed demonstrating the importance of polar stratospheric cloud.
Hideaki Nakajima, Ingo Wohltmann, Tobias Wegner, Masanori Takeda, Michael C. Pitts, Lamont R. Poole, Ralph Lehmann, Michelle L. Santee, and Markus Rex
Atmos. Chem. Phys., 16, 3311–3325, https://doi.org/10.5194/acp-16-3311-2016, https://doi.org/10.5194/acp-16-3311-2016, 2016
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This paper presents the first trial of analyzing amount of chlorine activation on different PSC compositions by using match analysis on trajectories initiated from PSC locations identified by CALIPSO/CALIOP measurements. The measured minor species such as HCl and ClO by MLS are compared with ATLAS chemistry-transport model (CTM) results. PSC growth to NAT, NAT/STS mixture, and ice were identified by different temperature decrease histories on trajectories.
D. M. Lienhard, A. J. Huisman, U. K. Krieger, Y. Rudich, C. Marcolli, B. P. Luo, D. L. Bones, J. P. Reid, A. T. Lambe, M. R. Canagaratna, P. Davidovits, T. B. Onasch, D. R. Worsnop, S. S. Steimer, T. Koop, and T. Peter
Atmos. Chem. Phys., 15, 13599–13613, https://doi.org/10.5194/acp-15-13599-2015, https://doi.org/10.5194/acp-15-13599-2015, 2015
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New data of water diffusivity in secondary organic aerosol (SOA) material and organic/inorganic model mixtures is presented over an extensive temperature range. Our data suggest that water diffusion in SOA is sufficiently fast so that it is unlikely to have significant consequences on the direct climatic effect under tropospheric conditions. Glass formation in SOA is unlikely to restrict homogeneous ice nucleation.
J.-X. Sheng, D. K. Weisenstein, B.-P. Luo, E. Rozanov, F. Arfeuille, and T. Peter
Atmos. Chem. Phys., 15, 11501–11512, https://doi.org/10.5194/acp-15-11501-2015, https://doi.org/10.5194/acp-15-11501-2015, 2015
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We have conducted a perturbed parameter model ensemble to investigate Mt.
Pinatubo's 1991 initial sulfur mass emission. Our results suggest that (a) the initial mass loading of the Pinatubo eruption is ~14 Mt of SO2; (b) the injection vertical distribution is strongly skewed towards the lower stratosphere, leading to a peak mass sulfur injection at 18-21 km; (c) the injection magnitude and height affect early southward transport of the volcanic cloud observed by SAGE II.
E. Hammer, N. Bukowiecki, B. P. Luo, U. Lohmann, C. Marcolli, E. Weingartner, U. Baltensperger, and C. R. Hoyle
Atmos. Chem. Phys., 15, 10309–10323, https://doi.org/10.5194/acp-15-10309-2015, https://doi.org/10.5194/acp-15-10309-2015, 2015
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An important quantity which determines aerosol activation and cloud formation is the effective peak supersaturation. The box model ZOMM was used to simulate the effective peak supersaturation experienced by an air parcel approaching a high-alpine research station in Switzerland. With the box model the sensitivity of the effective peak supersaturation to key aerosol and dynamical parameters was investigated.
E. Kienast-Sjögren, A. K. Miltenberger, B. P. Luo, and T. Peter
Atmos. Chem. Phys., 15, 7429–7447, https://doi.org/10.5194/acp-15-7429-2015, https://doi.org/10.5194/acp-15-7429-2015, 2015
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Sensitivities of Lagrangian cirrus modelling on input data uncertainties have been examined. We found a strong dependence on the temporal resolution of the trajectories and underlying numerical weather prediction (NWP) data as well as on the specific moisture content. Furthermore, we found a large day-to-day variability in the vertical wind spectrum, demonstrating the necessity to apply NWP models with high spatial and temporal resolution for Lagrangian cirrus modelling.
S. S. Steimer, U. K. Krieger, Y.-F. Te, D. M. Lienhard, A. J. Huisman, B. P. Luo, M. Ammann, and T. Peter
Atmos. Meas. Tech., 8, 2397–2408, https://doi.org/10.5194/amt-8-2397-2015, https://doi.org/10.5194/amt-8-2397-2015, 2015
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Atmospheric aerosol is often subject to supersaturated or supercooled conditions where bulk measurements are not possible. Here we demonstrate how measurements using single particle electrodynamic levitation combined with light scattering spectroscopy allow the retrieval of thermodynamic data, optical properties and water diffusivity of such metastable particles even when auxiliary bulk data are not available due to lack of sufficient amounts of sample.
W. Frey, S. Borrmann, F. Fierli, R. Weigel, V. Mitev, R. Matthey, F. Ravegnani, N. M. Sitnikov, A. Ulanovsky, and F. Cairo
Atmos. Chem. Phys., 14, 13223–13240, https://doi.org/10.5194/acp-14-13223-2014, https://doi.org/10.5194/acp-14-13223-2014, 2014
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This study presents in situ cloud microphysical observations obtained during a double flight in a Hector thunderstorm during the SCOUT-O3 campaign from Darwin, Northern Australia, in 2005. The measurements show a change of the micophysics with the storm's evolution. The clouds in the dissipating stage possess a high potential for affecting the humidity in the tropical tropopause layer.
S. Molleker, S. Borrmann, H. Schlager, B. Luo, W. Frey, M. Klingebiel, R. Weigel, M. Ebert, V. Mitev, R. Matthey, W. Woiwode, H. Oelhaf, A. Dörnbrack, G. Stratmann, J.-U. Grooß, G. Günther, B. Vogel, R. Müller, M. Krämer, J. Meyer, and F. Cairo
Atmos. Chem. Phys., 14, 10785–10801, https://doi.org/10.5194/acp-14-10785-2014, https://doi.org/10.5194/acp-14-10785-2014, 2014
A. Cirisan, B. P. Luo, I. Engel, F. G. Wienhold, M. Sprenger, U. K. Krieger, U. Weers, G. Romanens, G. Levrat, P. Jeannet, D. Ruffieux, R. Philipona, B. Calpini, P. Spichtinger, and T. Peter
Atmos. Chem. Phys., 14, 7341–7365, https://doi.org/10.5194/acp-14-7341-2014, https://doi.org/10.5194/acp-14-7341-2014, 2014
B. Hassler, I. Petropavlovskikh, J. Staehelin, T. August, P. K. Bhartia, C. Clerbaux, D. Degenstein, M. De Mazière, B. M. Dinelli, A. Dudhia, G. Dufour, S. M. Frith, L. Froidevaux, S. Godin-Beekmann, J. Granville, N. R. P. Harris, K. Hoppel, D. Hubert, Y. Kasai, M. J. Kurylo, E. Kyrölä, J.-C. Lambert, P. F. Levelt, C. T. McElroy, R. D. McPeters, R. Munro, H. Nakajima, A. Parrish, P. Raspollini, E. E. Remsberg, K. H. Rosenlof, A. Rozanov, T. Sano, Y. Sasano, M. Shiotani, H. G. J. Smit, G. Stiller, J. Tamminen, D. W. Tarasick, J. Urban, R. J. van der A, J. P. Veefkind, C. Vigouroux, T. von Clarmann, C. von Savigny, K. A. Walker, M. Weber, J. Wild, and J. M. Zawodny
Atmos. Meas. Tech., 7, 1395–1427, https://doi.org/10.5194/amt-7-1395-2014, https://doi.org/10.5194/amt-7-1395-2014, 2014
M. Rex, I. Wohltmann, T. Ridder, R. Lehmann, K. Rosenlof, P. Wennberg, D. Weisenstein, J. Notholt, K. Krüger, V. Mohr, and S. Tegtmeier
Atmos. Chem. Phys., 14, 4827–4841, https://doi.org/10.5194/acp-14-4827-2014, https://doi.org/10.5194/acp-14-4827-2014, 2014
S. Bucci, C. Cagnazzo, F. Cairo, L. Di Liberto, and F. Fierli
Atmos. Chem. Phys., 14, 4369–4381, https://doi.org/10.5194/acp-14-4369-2014, https://doi.org/10.5194/acp-14-4369-2014, 2014
I. Engel, B. P. Luo, S. M. Khaykin, F. G. Wienhold, H. Vömel, R. Kivi, C. R. Hoyle, J.-U. Grooß, M. C. Pitts, and T. Peter
Atmos. Chem. Phys., 14, 3231–3246, https://doi.org/10.5194/acp-14-3231-2014, https://doi.org/10.5194/acp-14-3231-2014, 2014
J.-U. Grooß, I. Engel, S. Borrmann, W. Frey, G. Günther, C. R. Hoyle, R. Kivi, B. P. Luo, S. Molleker, T. Peter, M. C. Pitts, H. Schlager, G. Stiller, H. Vömel, K. A. Walker, and R. Müller
Atmos. Chem. Phys., 14, 1055–1073, https://doi.org/10.5194/acp-14-1055-2014, https://doi.org/10.5194/acp-14-1055-2014, 2014
K. Kuribayashi, H. Sagawa, R. Lehmann, T. O. Sato, and Y. Kasai
Atmos. Chem. Phys., 14, 255–266, https://doi.org/10.5194/acp-14-255-2014, https://doi.org/10.5194/acp-14-255-2014, 2014
S. M. Khaykin, I. Engel, H. Vömel, I. M. Formanyuk, R. Kivi, L. I. Korshunov, M. Krämer, A. D. Lykov, S. Meier, T. Naebert, M. C. Pitts, M. L. Santee, N. Spelten, F. G. Wienhold, V. A. Yushkov, and T. Peter
Atmos. Chem. Phys., 13, 11503–11517, https://doi.org/10.5194/acp-13-11503-2013, https://doi.org/10.5194/acp-13-11503-2013, 2013
F. Arfeuille, B. P. Luo, P. Heckendorn, D. Weisenstein, J. X. Sheng, E. Rozanov, M. Schraner, S. Brönnimann, L. W. Thomason, and T. Peter
Atmos. Chem. Phys., 13, 11221–11234, https://doi.org/10.5194/acp-13-11221-2013, https://doi.org/10.5194/acp-13-11221-2013, 2013
I. Engel, B. P. Luo, M. C. Pitts, L. R. Poole, C. R. Hoyle, J.-U. Grooß, A. Dörnbrack, and T. Peter
Atmos. Chem. Phys., 13, 10769–10785, https://doi.org/10.5194/acp-13-10769-2013, https://doi.org/10.5194/acp-13-10769-2013, 2013
E. Castelli, B. M. Dinelli, S. Del Bianco, D. Gerber, B. P. Moyna, R. Siddans, B. J. Kerridge, and U. Cortesi
Atmos. Meas. Tech., 6, 2683–2701, https://doi.org/10.5194/amt-6-2683-2013, https://doi.org/10.5194/amt-6-2683-2013, 2013
A. Stenke, C. R. Hoyle, B. Luo, E. Rozanov, J. Gröbner, L. Maag, S. Brönnimann, and T. Peter
Atmos. Chem. Phys., 13, 9713–9729, https://doi.org/10.5194/acp-13-9713-2013, https://doi.org/10.5194/acp-13-9713-2013, 2013
C. R. Hoyle, I. Engel, B. P. Luo, M. C. Pitts, L. R. Poole, J.-U. Grooß, and T. Peter
Atmos. Chem. Phys., 13, 9577–9595, https://doi.org/10.5194/acp-13-9577-2013, https://doi.org/10.5194/acp-13-9577-2013, 2013
P. Raspollini, B. Carli, M. Carlotti, S. Ceccherini, A. Dehn, B. M. Dinelli, A. Dudhia, J.-M. Flaud, M. López-Puertas, F. Niro, J. J. Remedios, M. Ridolfi, H. Sembhi, L. Sgheri, and T. von Clarmann
Atmos. Meas. Tech., 6, 2419–2439, https://doi.org/10.5194/amt-6-2419-2013, https://doi.org/10.5194/amt-6-2419-2013, 2013
M. von Hobe, S. Bekki, S. Borrmann, F. Cairo, F. D'Amato, G. Di Donfrancesco, A. Dörnbrack, A. Ebersoldt, M. Ebert, C. Emde, I. Engel, M. Ern, W. Frey, S. Genco, S. Griessbach, J.-U. Grooß, T. Gulde, G. Günther, E. Hösen, L. Hoffmann, V. Homonnai, C. R. Hoyle, I. S. A. Isaksen, D. R. Jackson, I. M. Jánosi, R. L. Jones, K. Kandler, C. Kalicinsky, A. Keil, S. M. Khaykin, F. Khosrawi, R. Kivi, J. Kuttippurath, J. C. Laube, F. Lefèvre, R. Lehmann, S. Ludmann, B. P. Luo, M. Marchand, J. Meyer, V. Mitev, S. Molleker, R. Müller, H. Oelhaf, F. Olschewski, Y. Orsolini, T. Peter, K. Pfeilsticker, C. Piesch, M. C. Pitts, L. R. Poole, F. D. Pope, F. Ravegnani, M. Rex, M. Riese, T. Röckmann, B. Rognerud, A. Roiger, C. Rolf, M. L. Santee, M. Scheibe, C. Schiller, H. Schlager, M. Siciliani de Cumis, N. Sitnikov, O. A. Søvde, R. Spang, N. Spelten, F. Stordal, O. Sumińska-Ebersoldt, A. Ulanovski, J. Ungermann, S. Viciani, C. M. Volk, M. vom Scheidt, P. von der Gathen, K. Walker, T. Wegner, R. Weigel, S. Weinbruch, G. Wetzel, F. G. Wienhold, I. Wohltmann, W. Woiwode, I. A. K. Young, V. Yushkov, B. Zobrist, and F. Stroh
Atmos. Chem. Phys., 13, 9233–9268, https://doi.org/10.5194/acp-13-9233-2013, https://doi.org/10.5194/acp-13-9233-2013, 2013
A. Stenke, M. Schraner, E. Rozanov, T. Egorova, B. Luo, and T. Peter
Geosci. Model Dev., 6, 1407–1427, https://doi.org/10.5194/gmd-6-1407-2013, https://doi.org/10.5194/gmd-6-1407-2013, 2013
P. T. Verronen and R. Lehmann
Ann. Geophys., 31, 909–956, https://doi.org/10.5194/angeo-31-909-2013, https://doi.org/10.5194/angeo-31-909-2013, 2013
J. Gazeaux, C. Clerbaux, M. George, J. Hadji-Lazaro, J. Kuttippurath, P.-F. Coheur, D. Hurtmans, T. Deshler, M. Kovilakam, P. Campbell, V. Guidard, F. Rabier, and J.-N. Thépaut
Atmos. Meas. Tech., 6, 613–620, https://doi.org/10.5194/amt-6-613-2013, https://doi.org/10.5194/amt-6-613-2013, 2013
M. Carlotti, E. Arnone, E. Castelli, B. M. Dinelli, and E. Papandrea
Atmos. Meas. Tech., 6, 419–429, https://doi.org/10.5194/amt-6-419-2013, https://doi.org/10.5194/amt-6-419-2013, 2013
P. Cristofanelli, F. Fierli, A. Marinoni, F. Calzolari, R. Duchi, J. Burkhart, A. Stohl, M. Maione, J. Arduini, and P. Bonasoni
Atmos. Chem. Phys., 13, 15–30, https://doi.org/10.5194/acp-13-15-2013, https://doi.org/10.5194/acp-13-15-2013, 2013
Related subject area
Subject: Aerosols | Research Activity: Atmospheric Modelling and Data Analysis | Altitude Range: Stratosphere | Science Focus: Chemistry (chemical composition and reactions)
Stratospheric ozone depletion inside the volcanic plume shortly after the 2022 Hunga Tonga eruption
Analysis of the global atmospheric background sulfur budget in a multi-model framework
Effects of denitrification on the distributions of trace gas abundances in the polar regions: a comparison of WACCM with observations
Reconstructing volcanic radiative forcing since 1990, using a comprehensive emission inventory and spatially resolved sulfur injections from satellite data in a chemistry-climate model
Climate response to off-equatorial stratospheric sulfur injections in three Earth system models – Part 1: Experimental protocols and surface changes
Stratospheric ozone response to sulfate aerosol and solar dimming climate interventions based on the G6 Geoengineering Model Intercomparison Project (GeoMIP) simulations
The outflow of Asian biomass burning carbonaceous aerosol into the upper troposphere and lower stratosphere in spring: radiative effects seen in a global model
Mountain-wave-induced polar stratospheric clouds and their representation in the global chemistry model ICON-ART
Co-emission of volcanic sulfur and halogens amplifies volcanic effective radiative forcing
Potential of future stratospheric ozone loss in the midlatitudes under global warming and sulfate geoengineering
Evaluating the simulated radiative forcings, aerosol properties, and stratospheric warmings from the 1963 Mt Agung, 1982 El Chichón, and 1991 Mt Pinatubo volcanic aerosol clouds
The impact of recent changes in Asian anthropogenic emissions of SO2 on sulfate loading in the upper troposphere and lower stratosphere and the associated radiative changes
Mechanism of ozone loss under enhanced water vapour conditions in the mid-latitude lower stratosphere in summer
Multi-model comparison of the volcanic sulfate deposition from the 1815 eruption of Mt. Tambora
Impacts of Mt Pinatubo volcanic aerosol on the tropical stratosphere in chemistry–climate model simulations using CCMI and CMIP6 stratospheric aerosol data
Potential impact of carbonaceous aerosol on the upper troposphere and lower stratosphere (UTLS) and precipitation during Asian summer monsoon in a global model simulation
Vortex-wide chlorine activation by a mesoscale PSC event in the Arctic winter of 2009/10
Solar geoengineering using solid aerosol in the stratosphere
Aerosol microphysics simulations of the Mt.~Pinatubo eruption with the UM-UKCA composition-climate model
Modeling of 2008 Kasatochi volcanic sulfate direct radiative forcing: assimilation of OMI SO2 plume height data and comparison with MODIS and CALIOP observations
Microphysical simulations of sulfur burdens from stratospheric sulfur geoengineering
The role of carbonyl sulphide as a source of stratospheric sulphate aerosol and its impact on climate
Yunqian Zhu, Robert W. Portmann, Douglas Kinnison, Owen Brian Toon, Luis Millán, Jun Zhang, Holger Vömel, Simone Tilmes, Charles G. Bardeen, Xinyue Wang, Stephanie Evan, William J. Randel, and Karen H. Rosenlof
Atmos. Chem. Phys., 23, 13355–13367, https://doi.org/10.5194/acp-23-13355-2023, https://doi.org/10.5194/acp-23-13355-2023, 2023
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The 2022 Hunga Tonga eruption injected a large amount of water into the stratosphere. Ozone depletion was observed inside the volcanic plume. Chlorine and water vapor injected by this eruption exceeded the normal range, which made the ozone chemistry during this event occur at a higher temperature than polar ozone depletion. Unlike polar ozone chemistry where chlorine nitrate is more important, hypochlorous acid plays a large role in the in-plume chlorine balance and heterogeneous processes.
Christina V. Brodowsky, Timofei Sukhodolov, Gabriel Chiodo, Valentina Aquila, Slimane Bekki, Sandip S. Dhomse, Anton Laakso, Graham W. Mann, Ulrike Niemeier, Ilaria Quaglia, Eugene Rozanov, Anja Schmidt, Takashi Sekiya, Simone Tilmes, Claudia Timmreck, Sandro Vattioni, Daniele Visioni, Pengfei Yu, Yunqian Zhu, and Thomas Peter
EGUsphere, https://doi.org/10.5194/egusphere-2023-1655, https://doi.org/10.5194/egusphere-2023-1655, 2023
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The aerosol layer is an essential part of the climate system. We characterize the sulfur budget in a volcanically quiescent (background) setting, with a special focus on the sulfate aerosol layer, for the first time using a multi-model approach. The aim is to identify weak points in the representation of the atmospheric sulfur budget in an intercomparison of nine state-of-the-art coupled global circulation models.
Michael Weimer, Douglas E. Kinnison, Catherine Wilka, and Susan Solomon
Atmos. Chem. Phys., 23, 6849–6861, https://doi.org/10.5194/acp-23-6849-2023, https://doi.org/10.5194/acp-23-6849-2023, 2023
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We investigate the influence of the number density of nitric acid trihydrate (NAT) particles on associated trace gases in the lower stratosphere using data from a satellite, ozonesondes and simulations by a community chemistry climate model. By comparing probability density functions between observations and the model, we find that the standard NAT number density should be reduced for future simulations with the model.
Jennifer Schallock, Christoph Brühl, Christine Bingen, Michael Höpfner, Landon Rieger, and Jos Lelieveld
Atmos. Chem. Phys., 23, 1169–1207, https://doi.org/10.5194/acp-23-1169-2023, https://doi.org/10.5194/acp-23-1169-2023, 2023
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We characterized the influence of volcanic aerosols for the period 1990–2019 and established a volcanic SO2 emission inventory that includes more than 500 eruptions. From limb-based satellite observations of SO2 and extinction, we derive 3D plumes of SO2 perturbations and injected mass by a novel method. We calculate instantaneous radiative forcing with a comprehensive chemisty climate model. Our results show that smaller eruptions can also contribute to the stratospheric aerosol forcing.
Daniele Visioni, Ewa M. Bednarz, Walker R. Lee, Ben Kravitz, Andy Jones, Jim M. Haywood, and Douglas G. MacMartin
Atmos. Chem. Phys., 23, 663–685, https://doi.org/10.5194/acp-23-663-2023, https://doi.org/10.5194/acp-23-663-2023, 2023
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The paper constitutes Part 1 of a study performing a first systematic inter-model comparison of the atmospheric responses to stratospheric sulfate aerosol injections (SAIs) at various latitudes as simulated by three state-of-the-art Earth system models. We identify similarities and differences in the modeled aerosol burden, investigate the differences in the aerosol approaches between the models, and ultimately show the differences produced in surface climate, temperature and precipitation.
Simone Tilmes, Daniele Visioni, Andy Jones, James Haywood, Roland Séférian, Pierre Nabat, Olivier Boucher, Ewa Monica Bednarz, and Ulrike Niemeier
Atmos. Chem. Phys., 22, 4557–4579, https://doi.org/10.5194/acp-22-4557-2022, https://doi.org/10.5194/acp-22-4557-2022, 2022
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This study assesses the impacts of climate interventions, using stratospheric sulfate aerosol and solar dimming on stratospheric ozone, based on three Earth system models with interactive stratospheric chemistry. The climate interventions have been applied to a high emission (baseline) scenario in order to reach global surface temperatures of a medium emission scenario. We find significant increases and decreases in total column ozone, depending on regions and seasons.
Prashant Chavan, Suvarna Fadnavis, Tanusri Chakroborty, Christopher E. Sioris, Sabine Griessbach, and Rolf Müller
Atmos. Chem. Phys., 21, 14371–14384, https://doi.org/10.5194/acp-21-14371-2021, https://doi.org/10.5194/acp-21-14371-2021, 2021
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Biomass burning (BB) over Asia is a strong source of carbonaceous aerosols during spring. Here, we show an outflow of Asian BB carbonaceous aerosols into the UTLS. These aerosols enhance atmospheric heating and produce circulation changes that lead to the enhancement of water vapor in the UTLS over the tropics. In the stratosphere, water vapor is further transported to the South Pole by the Brewer–Dobson circulation. Enhancement of water vapor in the UTLS has implications for climate change.
Michael Weimer, Jennifer Buchmüller, Lars Hoffmann, Ole Kirner, Beiping Luo, Roland Ruhnke, Michael Steiner, Ines Tritscher, and Peter Braesicke
Atmos. Chem. Phys., 21, 9515–9543, https://doi.org/10.5194/acp-21-9515-2021, https://doi.org/10.5194/acp-21-9515-2021, 2021
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We show that we are able to directly simulate polar stratospheric clouds formed locally in a mountain wave and represent their effect on the ozone chemistry with the global atmospheric chemistry model ICON-ART. Thus, we show the first simulations that close the gap between directly resolved mountain-wave-induced polar stratospheric clouds and their representation at coarse global resolutions.
John Staunton-Sykes, Thomas J. Aubry, Youngsub M. Shin, James Weber, Lauren R. Marshall, Nathan Luke Abraham, Alex Archibald, and Anja Schmidt
Atmos. Chem. Phys., 21, 9009–9029, https://doi.org/10.5194/acp-21-9009-2021, https://doi.org/10.5194/acp-21-9009-2021, 2021
Sabine Robrecht, Bärbel Vogel, Simone Tilmes, and Rolf Müller
Atmos. Chem. Phys., 21, 2427–2455, https://doi.org/10.5194/acp-21-2427-2021, https://doi.org/10.5194/acp-21-2427-2021, 2021
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Column ozone protects life on Earth from radiation damage. Stratospheric chlorine compounds cause immense ozone loss in polar winter. Whether similar loss processes can occur in the lower stratosphere above North America today or in future is a matter of debate. We show that these ozone loss processes are very unlikely today or in future independently of whether sulfate geoengineering is applied and that less than 0.1 % of column ozone would be destroyed by this process in any future scenario.
Sandip S. Dhomse, Graham W. Mann, Juan Carlos Antuña Marrero, Sarah E. Shallcross, Martyn P. Chipperfield, Kenneth S. Carslaw, Lauren Marshall, N. Luke Abraham, and Colin E. Johnson
Atmos. Chem. Phys., 20, 13627–13654, https://doi.org/10.5194/acp-20-13627-2020, https://doi.org/10.5194/acp-20-13627-2020, 2020
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We confirm downward adjustment of SO2 emission to simulate the Pinatubo aerosol cloud with aerosol microphysics models. Similar adjustment is also needed to simulate the El Chichón and Agung volcanic cloud, indicating potential missing removal or vertical redistribution process in models. Important inhomogeneities in the CMIP6 forcing datasets after Agung and El Chichón eruptions are difficult to reconcile. Quasi-biennial oscillation plays an important role in modifying stratospheric warming.
Suvarna Fadnavis, Rolf Müller, Gayatry Kalita, Matthew Rowlinson, Alexandru Rap, Jui-Lin Frank Li, Blaž Gasparini, and Anton Laakso
Atmos. Chem. Phys., 19, 9989–10008, https://doi.org/10.5194/acp-19-9989-2019, https://doi.org/10.5194/acp-19-9989-2019, 2019
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This paper highlights the impact of Asian anthropogenic emission changes in SO2 on sulfate loading in the Asian upper troposphere–lower stratosphere from a global chemistry–climate model and satellite remote sensing. Estimated seasonal mean direct radiative forcing at the top of the atmosphere induced by the increase in Indian SO2 is −0.2–−1.5 W m2 over India. Chinese SO2 emission reduction leads to a positive radiative forcing of ~0.6–6 W m2 over China. It will likely decrease Indian rainfall.
Sabine Robrecht, Bärbel Vogel, Jens-Uwe Grooß, Karen Rosenlof, Troy Thornberry, Andrew Rollins, Martina Krämer, Lance Christensen, and Rolf Müller
Atmos. Chem. Phys., 19, 5805–5833, https://doi.org/10.5194/acp-19-5805-2019, https://doi.org/10.5194/acp-19-5805-2019, 2019
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The potential destruction of stratospheric ozone in the mid-latitudes has been discussed recently. We analysed this ozone loss mechanism and its sensitivities. In a certain temperature range, we found a threshold in water vapour, which has to be exceeded for ozone loss to occur. We show the dependence of this water vapour threshold on temperature, sulfate content and air composition. This study provides a basis to estimate the impact of potential sulphate geoengineering on stratospheric ozone.
Lauren Marshall, Anja Schmidt, Matthew Toohey, Ken S. Carslaw, Graham W. Mann, Michael Sigl, Myriam Khodri, Claudia Timmreck, Davide Zanchettin, William T. Ball, Slimane Bekki, James S. A. Brooke, Sandip Dhomse, Colin Johnson, Jean-Francois Lamarque, Allegra N. LeGrande, Michael J. Mills, Ulrike Niemeier, James O. Pope, Virginie Poulain, Alan Robock, Eugene Rozanov, Andrea Stenke, Timofei Sukhodolov, Simone Tilmes, Kostas Tsigaridis, and Fiona Tummon
Atmos. Chem. Phys., 18, 2307–2328, https://doi.org/10.5194/acp-18-2307-2018, https://doi.org/10.5194/acp-18-2307-2018, 2018
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We use four global aerosol models to compare the simulated sulfate deposition from the 1815 Mt. Tambora eruption to ice core records. Inter-model volcanic sulfate deposition differs considerably. Volcanic sulfate deposited on polar ice sheets is used to estimate the atmospheric sulfate burden and subsequently radiative forcing of historic eruptions. Our results suggest that deriving such relationships from model simulations may be associated with greater uncertainties than previously thought.
Laura E. Revell, Andrea Stenke, Beiping Luo, Stefanie Kremser, Eugene Rozanov, Timofei Sukhodolov, and Thomas Peter
Atmos. Chem. Phys., 17, 13139–13150, https://doi.org/10.5194/acp-17-13139-2017, https://doi.org/10.5194/acp-17-13139-2017, 2017
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Compiling stratospheric aerosol data sets after a major volcanic eruption is difficult as the stratosphere becomes too optically opaque for satellite instruments to measure accurately. We performed ensemble chemistry–climate model simulations with two stratospheric aerosol data sets compiled for two international modelling activities and compared the simulated volcanic aerosol-induced effects from the 1991 Mt Pinatubo eruption on tropical stratospheric temperature and ozone with observations.
Suvarna Fadnavis, Gayatry Kalita, K. Ravi Kumar, Blaž Gasparini, and Jui-Lin Frank Li
Atmos. Chem. Phys., 17, 11637–11654, https://doi.org/10.5194/acp-17-11637-2017, https://doi.org/10.5194/acp-17-11637-2017, 2017
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In this study, the model simulations show that monsoon convection over the Bay of Bengal, the South China Sea and southern flanks of the Himalayas transports Asian carbonaceous aerosol into the UTLS. Carbonaceous aerosol induces enhancement in heating rate, vertical velocity and water vapor transport in the UTLS. Doubling of carbonaceous aerosols creates an anomalous warming over the TP. It generates monsoon Hadley circulation and thus increases precipitation over India and northeast China.
Tobias Wegner, Michael C. Pitts, Lamont R. Poole, Ines Tritscher, Jens-Uwe Grooß, and Hideaki Nakajima
Atmos. Chem. Phys., 16, 4569–4577, https://doi.org/10.5194/acp-16-4569-2016, https://doi.org/10.5194/acp-16-4569-2016, 2016
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Satellite observations are used to constrain areas with large backscatter values areas inside the polar vortex. Surface area is derived from these observations and used in heterogeneous modeling. Satellite gas species observations show a decrease in HCl downwind of areas with large surface area density indicating heterogeneous processing inside these areas. This decrease can only be simulated if a realistic surface area is assumed demonstrating the importance of polar stratospheric cloud.
D. K. Weisenstein, D. W. Keith, and J. A. Dykema
Atmos. Chem. Phys., 15, 11835–11859, https://doi.org/10.5194/acp-15-11835-2015, https://doi.org/10.5194/acp-15-11835-2015, 2015
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We investigate stratospheric aerosol geoengineering with solid particle injection by modeling the fractal structure of alumina aerosols and their interaction with background sulfate. We analyze the efficacy (W m^-2 of radiative forcing per megaton of injection) and risks (ozone loss, s) for both alumina and diamond particles as a function of injected monomer radius, finding 240nm alumina and 160nm diamond optimal. We discuss the limitations of our 2-D model study and associated uncertainties.
S. S. Dhomse, K. M. Emmerson, G. W. Mann, N. Bellouin, K. S. Carslaw, M. P. Chipperfield, R. Hommel, N. L. Abraham, P. Telford, P. Braesicke, M. Dalvi, C. E. Johnson, F. O'Connor, O. Morgenstern, J. A. Pyle, T. Deshler, J. M. Zawodny, and L. W. Thomason
Atmos. Chem. Phys., 14, 11221–11246, https://doi.org/10.5194/acp-14-11221-2014, https://doi.org/10.5194/acp-14-11221-2014, 2014
J. Wang, S. Park, J. Zeng, C. Ge, K. Yang, S. Carn, N. Krotkov, and A. H. Omar
Atmos. Chem. Phys., 13, 1895–1912, https://doi.org/10.5194/acp-13-1895-2013, https://doi.org/10.5194/acp-13-1895-2013, 2013
J. M. English, O. B. Toon, and M. J. Mills
Atmos. Chem. Phys., 12, 4775–4793, https://doi.org/10.5194/acp-12-4775-2012, https://doi.org/10.5194/acp-12-4775-2012, 2012
C. Brühl, J. Lelieveld, P. J. Crutzen, and H. Tost
Atmos. Chem. Phys., 12, 1239–1253, https://doi.org/10.5194/acp-12-1239-2012, https://doi.org/10.5194/acp-12-1239-2012, 2012
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Short summary
We investigated chemical and microphysical processes in the late winter Antarctic stratosphere, for the first time (to our knowledge) coupling a detailed microphysical box model to a chemistry model.
Model results have been compared with in situ and remote sensing measurements of particles along trajectories.
Our goal is to contribute to the most recent discussion of the relative role of PSC and liquid (background) aerosol in the ozone depletion.
We investigated chemical and microphysical processes in the late winter Antarctic stratosphere,...
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