Articles | Volume 22, issue 6
https://doi.org/10.5194/acp-22-3967-2022
© Author(s) 2022. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/acp-22-3967-2022
© Author(s) 2022. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Research article
| 
28 Mar 2022
Research article |
| 28 Mar 2022
| 28 Mar 2022
Five-satellite-sensor study of the rapid decline of wildfire smoke in the stratosphere
Bengt G. Martinsson
CORRESPONDING AUTHOR
Department of Physics, Lund University, Lund, Sweden
Johan Friberg
Department of Physics, Lund University, Lund, Sweden
Oscar S. Sandvik
Department of Physics, Lund University, Lund, Sweden
Moa K. Sporre
Department of Physics, Lund University, Lund, Sweden
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Johan Friberg, Bengt G. Martinsson, and Moa K. Sporre
Atmos. Chem. Phys., 23, 12557–12570, https://doi.org/10.5194/acp-23-12557-2023, https://doi.org/10.5194/acp-23-12557-2023, 2023
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We study the short- and long-term stratospheric impact of smoke from the massive Australian wildfires in Dec 2019–Jan 2020 using four satellite sensors. Smoke entered the stratosphere rapidly via transport by firestorms, as well as weeks after the fires. The smoke particle properties evolved over time together with rapidly decreasing stratospheric aerosol load, suggesting photolytic loss of organics in the smoke particles. The depletion rate was estimated to a half-life (e folding) of 10 (14) d.
Oscar S. Sandvik, Johan Friberg, Moa K. Sporre, and Bengt G. Martinsson
Atmos. Meas. Tech., 14, 7153–7165, https://doi.org/10.5194/amt-14-7153-2021, https://doi.org/10.5194/amt-14-7153-2021, 2021
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A method to form SO2 profiles in the stratosphere with high vertical resolution following volcanic eruptions is introduced. The method combines space-based high-resolution vertical aerosol profiles and SO2 measurements the first 2 weeks after an eruption with air mass trajectory analyses. The SO2 is located at higher altitude than in most previous studies. The detailed resolution of the SO2 profile is unprecedented compared to other methods.
Franz Slemr, Andreas Weigelt, Ralf Ebinghaus, Johannes Bieser, Carl A. M. Brenninkmeijer, Armin Rauthe-Schöch, Markus Hermann, Bengt G. Martinsson, Peter van Velthoven, Harald Bönisch, Marco Neumaier, Andreas Zahn, and Helmut Ziereis
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Total and elemental mercury were measured in the upper troposphere and lower stratosphere onboard a passenger aircraft. Their concentrations in the upper troposphere were comparable implying low concentrations of oxidized mercury in this region. Large scale seasonally dependent influence of emissions from biomass burning was also observed. Their distributions in the lower stratosphere implies a long stratospheric lifetime, which precludes significant mercury oxidation by ozone.
Johan Friberg, Bengt G. Martinsson, Sandra M. Andersson, and Oscar S. Sandvik
Atmos. Chem. Phys., 18, 11149–11169, https://doi.org/10.5194/acp-18-11149-2018, https://doi.org/10.5194/acp-18-11149-2018, 2018
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During 2006–2015 volcanism contributed 40 % of the stratospheric aerosol load. We compute the AOD (aerosol optical depth) of the stratosphere (from the tropopause to 35 km altitude) using new techniques of handling CALIOP data. Regional and global AODs are presented for the entire stratosphere in relation to transport patterns, and the AOD is presented for three stratospheric layers: the LMS, the potential temperature range of 380 to 470 K, and altitudes above the 470 K isentrope.
Bengt G. Martinsson, Johan Friberg, Oscar S. Sandvik, Markus Hermann, Peter F. J. van Velthoven, and Andreas Zahn
Atmos. Chem. Phys., 17, 10937–10953, https://doi.org/10.5194/acp-17-10937-2017, https://doi.org/10.5194/acp-17-10937-2017, 2017
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We find that the aerosol of the lowermost stratosphere has a considerable climate forcing. The upper tropospheric (UT) particulate sulfur is strongly influenced by stratospheric sources the first half of the year, whereas tropospheric sources dominate in fall; 50 % of the UT particulate sulfur (S) was found to be stratospheric at background condition, and 70 % under moderate influence from volcanism. The Asian monsoon is found to be an important tropospheric source of S in the NH extratropical UT.
M. I. A. Berghof, G. P. Frank, S. Sjogren, and B. G. Martinsson
Atmos. Meas. Tech., 7, 877–886, https://doi.org/10.5194/amt-7-877-2014, https://doi.org/10.5194/amt-7-877-2014, 2014
S. Sjogren, G. P. Frank, M. I. A. Berghof, and B. G. Martinsson
Atmos. Meas. Tech., 6, 349–357, https://doi.org/10.5194/amt-6-349-2013, https://doi.org/10.5194/amt-6-349-2013, 2013
Carl Svenhag, Moa K. Sporre, Tinja Olenius, Daniel Yazgi, Sara M. Blichner, Lars P. Nieradzik, and Pontus Roldin
Geosci. Model Dev., 17, 4923–4942, https://doi.org/10.5194/gmd-17-4923-2024, https://doi.org/10.5194/gmd-17-4923-2024, 2024
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Our research shows the importance of modeling new particle formation (NPF) and growth of particles in the atmosphere on a global scale, as they influence the outcomes of clouds and our climate. With the global model EC-Earth3 we show that using a new method for NPF modeling, which includes new detailed processes with NH3 and H2SO4, significantly impacts the number of particles in the air and clouds and changes the radiation balance of the same magnitude as anthropogenic greenhouse emissions.
Emma Axebrink, Moa K. Sporre, and Johan Friberg
EGUsphere, https://doi.org/10.5194/egusphere-2024-1448, https://doi.org/10.5194/egusphere-2024-1448, 2024
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We investigate the importance of using high vertical resolution (HR) SO2 data when simulating a volcanic eruptions’ impact on the stratospheric aerosol load and climate, using WACCM, and compare simulations with aerosol observations from CALIOP. Simulations with HR SO2 data match the observations well, whereas simulations with the model’s default low-resolution (LR) data underestimates the aerosol load by ~50 %. The resulting climate cooling is twice as high for the HR than the LR SO2 data.
Johan Friberg, Bengt G. Martinsson, and Moa K. Sporre
Atmos. Chem. Phys., 23, 12557–12570, https://doi.org/10.5194/acp-23-12557-2023, https://doi.org/10.5194/acp-23-12557-2023, 2023
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We study the short- and long-term stratospheric impact of smoke from the massive Australian wildfires in Dec 2019–Jan 2020 using four satellite sensors. Smoke entered the stratosphere rapidly via transport by firestorms, as well as weeks after the fires. The smoke particle properties evolved over time together with rapidly decreasing stratospheric aerosol load, suggesting photolytic loss of organics in the smoke particles. The depletion rate was estimated to a half-life (e folding) of 10 (14) d.
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Atmos. Chem. Phys., 21, 17243–17265, https://doi.org/10.5194/acp-21-17243-2021, https://doi.org/10.5194/acp-21-17243-2021, 2021
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In this study we quantify how a new way of modeling the formation of new particles in the atmosphere affects the estimated cooling from aerosol–cloud interactions since pre-industrial times. Our improved scheme merges two common approaches to aerosol modeling: a sectional scheme for treating early growth and the pre-existing modal scheme in NorESM. We find that the cooling from aerosol–cloud interactions since pre-industrial times is reduced by 10 % when the new scheme is used.
Oscar S. Sandvik, Johan Friberg, Moa K. Sporre, and Bengt G. Martinsson
Atmos. Meas. Tech., 14, 7153–7165, https://doi.org/10.5194/amt-14-7153-2021, https://doi.org/10.5194/amt-14-7153-2021, 2021
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A method to form SO2 profiles in the stratosphere with high vertical resolution following volcanic eruptions is introduced. The method combines space-based high-resolution vertical aerosol profiles and SO2 measurements the first 2 weeks after an eruption with air mass trajectory analyses. The SO2 is located at higher altitude than in most previous studies. The detailed resolution of the SO2 profile is unprecedented compared to other methods.
Sara M. Blichner, Moa K. Sporre, Risto Makkonen, and Terje K. Berntsen
Geosci. Model Dev., 14, 3335–3359, https://doi.org/10.5194/gmd-14-3335-2021, https://doi.org/10.5194/gmd-14-3335-2021, 2021
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Aerosol–cloud interactions are the largest contributor to climate forcing uncertainty. In this study we combine two common approaches to aerosol representation in global models: a sectional scheme, which is closer to first principals, for the smallest particles forming in the atmosphere and a log-modal scheme, which is faster, for the larger particles. With this approach, we improve the aerosol representation compared to observations, while only increasing the computational cost by 15 %.
Stina Ausmeel, Axel Eriksson, Erik Ahlberg, Moa K. Sporre, Mårten Spanne, and Adam Kristensson
Atmos. Chem. Phys., 20, 9135–9151, https://doi.org/10.5194/acp-20-9135-2020, https://doi.org/10.5194/acp-20-9135-2020, 2020
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Emissions from shipping have an impact on air quality, especially in coastal areas. We have measured properties of the airborne particles in several plumes from ships that are sailing within an Emission Control Area. Individual ships showed large variability in contribution to total particle mass and nitrogen dioxide. Organics and sulfate dominated the particle mass, and most plumes contained very little or no soot. We also present recommendations for future stationary ship plume measurements.
Moa K. Sporre, Sara M. Blichner, Roland Schrödner, Inger H. H. Karset, Terje K. Berntsen, Twan van Noije, Tommi Bergman, Declan O'Donnell, and Risto Makkonen
Atmos. Chem. Phys., 20, 8953–8973, https://doi.org/10.5194/acp-20-8953-2020, https://doi.org/10.5194/acp-20-8953-2020, 2020
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We investigate how emissions and parameters in current
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Giulia Saponaro, Moa K. Sporre, David Neubauer, Harri Kokkola, Pekka Kolmonen, Larisa Sogacheva, Antti Arola, Gerrit de Leeuw, Inger H. H. Karset, Ari Laaksonen, and Ulrike Lohmann
Atmos. Chem. Phys., 20, 1607–1626, https://doi.org/10.5194/acp-20-1607-2020, https://doi.org/10.5194/acp-20-1607-2020, 2020
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The understanding of cloud processes is based on the quality of the representation of cloud properties. We compared cloud parameters from three models with satellite observations. We report on the performance of each data source, highlighting strengths and deficiencies, which should be considered when deriving the effect of aerosols on cloud properties.
Moa K. Sporre, Sara M. Blichner, Inger H. H. Karset, Risto Makkonen, and Terje K. Berntsen
Atmos. Chem. Phys., 19, 4763–4782, https://doi.org/10.5194/acp-19-4763-2019, https://doi.org/10.5194/acp-19-4763-2019, 2019
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In this study, an Earth system model has been used to investigate climate feedbacks associated with increasing BVOC emissions due to higher CO2 concentrations and temperatures. Higher BVOC emissions associated with a changed climate are found to induce an important negative climate feedback through increased aerosol formation and resulting changes in cloud properties. This feedback is found to have the potential to offset about 13 % of the radiative forcing associated with a doubling of CO2.
Franz Slemr, Andreas Weigelt, Ralf Ebinghaus, Johannes Bieser, Carl A. M. Brenninkmeijer, Armin Rauthe-Schöch, Markus Hermann, Bengt G. Martinsson, Peter van Velthoven, Harald Bönisch, Marco Neumaier, Andreas Zahn, and Helmut Ziereis
Atmos. Chem. Phys., 18, 12329–12343, https://doi.org/10.5194/acp-18-12329-2018, https://doi.org/10.5194/acp-18-12329-2018, 2018
Short summary
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Total and elemental mercury were measured in the upper troposphere and lower stratosphere onboard a passenger aircraft. Their concentrations in the upper troposphere were comparable implying low concentrations of oxidized mercury in this region. Large scale seasonally dependent influence of emissions from biomass burning was also observed. Their distributions in the lower stratosphere implies a long stratospheric lifetime, which precludes significant mercury oxidation by ozone.
Johan Friberg, Bengt G. Martinsson, Sandra M. Andersson, and Oscar S. Sandvik
Atmos. Chem. Phys., 18, 11149–11169, https://doi.org/10.5194/acp-18-11149-2018, https://doi.org/10.5194/acp-18-11149-2018, 2018
Short summary
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During 2006–2015 volcanism contributed 40 % of the stratospheric aerosol load. We compute the AOD (aerosol optical depth) of the stratosphere (from the tropopause to 35 km altitude) using new techniques of handling CALIOP data. Regional and global AODs are presented for the entire stratosphere in relation to transport patterns, and the AOD is presented for three stratospheric layers: the LMS, the potential temperature range of 380 to 470 K, and altitudes above the 470 K isentrope.
Johan Martinsson, Guillaume Monteil, Moa K. Sporre, Anne Maria Kaldal Hansen, Adam Kristensson, Kristina Eriksson Stenström, Erik Swietlicki, and Marianne Glasius
Atmos. Chem. Phys., 17, 11025–11040, https://doi.org/10.5194/acp-17-11025-2017, https://doi.org/10.5194/acp-17-11025-2017, 2017
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This study attempts to link observations of biogenic organic compounds found in atmospheric particles to landscape exposure of the incoming air mass. The results revealed that several of the observed compounds were connected to exposure of coniferous forests. There were also a number of landscape types that did not contribute to the biogenic organic compounds, sea and ocean as an example. This type of methodology may be important in order to study land use changes impact on air quality.
Bengt G. Martinsson, Johan Friberg, Oscar S. Sandvik, Markus Hermann, Peter F. J. van Velthoven, and Andreas Zahn
Atmos. Chem. Phys., 17, 10937–10953, https://doi.org/10.5194/acp-17-10937-2017, https://doi.org/10.5194/acp-17-10937-2017, 2017
Short summary
Short summary
We find that the aerosol of the lowermost stratosphere has a considerable climate forcing. The upper tropospheric (UT) particulate sulfur is strongly influenced by stratospheric sources the first half of the year, whereas tropospheric sources dominate in fall; 50 % of the UT particulate sulfur (S) was found to be stratospheric at background condition, and 70 % under moderate influence from volcanism. The Asian monsoon is found to be an important tropospheric source of S in the NH extratropical UT.
Johan Martinsson, Hafiz Abdul Azeem, Moa K. Sporre, Robert Bergström, Erik Ahlberg, Emilie Öström, Adam Kristensson, Erik Swietlicki, and Kristina Eriksson Stenström
Atmos. Chem. Phys., 17, 4265–4281, https://doi.org/10.5194/acp-17-4265-2017, https://doi.org/10.5194/acp-17-4265-2017, 2017
Short summary
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In this study we have focused our attention on the sources atmospheric carbon particles. More specifically, we evaluate a fast and inexpensive method which determines the source of these particles by utilizing light absorption by the particles. We found that this method is suitable for source estimation by comparing it to another method based on carbon isotopes and chemical tracer molecules. Cheap and fast methods based on light absorption can be utilized widely to deduce particle sources.
Moa K. Sporre, Ewan J. O'Connor, Nina Håkansson, Anke Thoss, Erik Swietlicki, and Tuukka Petäjä
Atmos. Meas. Tech., 9, 3193–3203, https://doi.org/10.5194/amt-9-3193-2016, https://doi.org/10.5194/amt-9-3193-2016, 2016
Short summary
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Satellite measurements of cloud top height and liquid water path are compared to ground-based remote sensing to evaluate the satellite retrievals. The overall performance of the satellite retrievals of cloud top height are good, but they become more problematic when several layers of clouds are present. The liquid water path retrievals also agree well, and the average differences are within the estimated measurement uncertainties.
M. K. Sporre, E. Swietlicki, P. Glantz, and M. Kulmala
Atmos. Chem. Phys., 14, 12167–12179, https://doi.org/10.5194/acp-14-12167-2014, https://doi.org/10.5194/acp-14-12167-2014, 2014
B. G. Martinsson, J. Friberg, S. M. Andersson, A. Weigelt, M. Hermann, D. Assmann, J. Voigtländer, C. A. M. Brenninkmeijer, P. J. F. van Velthoven, and A. Zahn
Atmos. Meas. Tech., 7, 2581–2596, https://doi.org/10.5194/amt-7-2581-2014, https://doi.org/10.5194/amt-7-2581-2014, 2014
M. I. A. Berghof, G. P. Frank, S. Sjogren, and B. G. Martinsson
Atmos. Meas. Tech., 7, 877–886, https://doi.org/10.5194/amt-7-877-2014, https://doi.org/10.5194/amt-7-877-2014, 2014
M. K. Sporre, E. Swietlicki, P. Glantz, and M. Kulmala
Atmos. Chem. Phys., 14, 2203–2217, https://doi.org/10.5194/acp-14-2203-2014, https://doi.org/10.5194/acp-14-2203-2014, 2014
S. M. Andersson, B. G. Martinsson, J. Friberg, C. A. M. Brenninkmeijer, A. Rauthe-Schöch, M. Hermann, P. F. J. van Velthoven, and A. Zahn
Atmos. Chem. Phys., 13, 1781–1796, https://doi.org/10.5194/acp-13-1781-2013, https://doi.org/10.5194/acp-13-1781-2013, 2013
S. Sjogren, G. P. Frank, M. I. A. Berghof, and B. G. Martinsson
Atmos. Meas. Tech., 6, 349–357, https://doi.org/10.5194/amt-6-349-2013, https://doi.org/10.5194/amt-6-349-2013, 2013
Related subject area
Subject: Aerosols | Research Activity: Remote Sensing | Altitude Range: Stratosphere | Science Focus: Physics (physical properties and processes)
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Transport of the 2017 Canadian wildfire plume to the tropics via the Asian monsoon circulation
Lidar observations of pyrocumulonimbus smoke plumes in the UTLS over Tomsk (Western Siberia, Russia) from 2000 to 2017
Long-range-transported Canadian smoke plumes in the lower stratosphere over northern France
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Volcanic impact on the climate – the stratospheric aerosol load in the period 2006–2015
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30-year lidar observations of the stratospheric aerosol layer state over Tomsk (Western Siberia, Russia)
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Interannual variations of early winter Antarctic polar stratospheric cloud formation and nitric acid observed by CALIOP and MLS
Spectroscopic evidence of large aspherical β-NAT particles involved in denitrification in the December 2011 Arctic stratosphere
CALIOP near-real-time backscatter products compared to EARLINET data
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Dispersion of the Nabro volcanic plume and its relation to the Asian summer monsoon
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Odin-OSIRIS stratospheric aerosol data product and SAGE III intercomparison
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Radiosonde stratospheric temperatures at Dumont d'Urville (Antarctica): trends and link with polar stratospheric clouds
An evaluation of the SAGE III version 4 aerosol extinction coefficient and water vapor data products
Yun He, Dongzhe Jing, Zhenping Yin, Kevin Ohneiser, and Fan Yi
Atmos. Chem. Phys., 24, 11431–11450, https://doi.org/10.5194/acp-24-11431-2024, https://doi.org/10.5194/acp-24-11431-2024, 2024
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We present a long-term ground-based lidar observation of stratospheric aerosols at a mid-latitude site, Wuhan, in central China, from 2010 to 2021. We observed a stratospheric background period from 2013 to mid-2017, along with several perturbations from volcanic aerosols and wildfire-induced smoke. In summer, injected stratospheric aerosols are found to be captured by the Asian monsoon anticyclone, resulting in prolonged residence and regional transport in the mid-latitudes of East Asia.
Nelson Bègue, Alexandre Baron, Gisèle Krysztofiak, Gwenaël Berthet, Corinna Kloss, Fabrice Jégou, Sergey Khaykin, Marion Ranaivombola, Tristan Millet, Thierry Portafaix, Valentin Duflot, Philippe Keckhut, Hélène Vérèmes, Guillaume Payen, Mahesh Kumar Sha, Pierre-François Coheur, Cathy Clerbaux, Michaël Sicard, Tetsu Sakai, Richard Querel, Ben Liley, Dan Smale, Isamu Morino, Osamu Uchino, Tomohiro Nagai, Penny Smale, John Robinson, and Hassan Bencherif
Atmos. Chem. Phys., 24, 8031–8048, https://doi.org/10.5194/acp-24-8031-2024, https://doi.org/10.5194/acp-24-8031-2024, 2024
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During the 2020 austral summer, the pristine atmosphere of the southwest Indian Ocean basin experienced significant perturbations. Numerical models indicated that the lower-stratospheric aerosol content was influenced by the intense and persistent stratospheric aerosol layer generated during the 2019–2020 extreme Australian bushfire events. Ground-based observations at Réunion confirmed the simultaneous presence of African and Australian aerosol layers.
Sandra Graßl, Christoph Ritter, Ines Tritscher, and Bärbel Vogel
Atmos. Chem. Phys., 24, 7535–7557, https://doi.org/10.5194/acp-24-7535-2024, https://doi.org/10.5194/acp-24-7535-2024, 2024
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Arctic lidar data for 1 year are compared with global modeling of aerosol tracers in the stratosphere. A trend in the aerosol backscatter can be found. These observations are further compared with a model study to investigate the aerosol origin of the observed arctic aerosol. We found a correlation with increased backscatter signal during summer and early autumn and pathways from the Southeast Asian monsoon region and remains of the Asian tropopause aerosol layer in the Arctic.
Jean-Paul Vernier, Thomas J. Aubry, Claudia Timmreck, Anja Schmidt, Lieven Clarisse, Fred Prata, Nicolas Theys, Andrew T. Prata, Graham Mann, Hyundeok Choi, Simon Carn, Richard Rigby, Susan C. Loughlin, and John A. Stevenson
Atmos. Chem. Phys., 24, 5765–5782, https://doi.org/10.5194/acp-24-5765-2024, https://doi.org/10.5194/acp-24-5765-2024, 2024
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The 2019 Raikoke eruption (Kamchatka, Russia) generated one of the largest emissions of particles and gases into the stratosphere since the 1991 Mt. Pinatubo eruption. The Volcano Response (VolRes) initiative, an international effort, provided a platform for the community to share information about this eruption and assess its climate impact. The eruption led to a minor global surface cooling of 0.02 °C in 2020 which is negligible relative to warming induced by human greenhouse gas emissions.
Thomas Trickl, Hannes Vogelmann, Michael D. Fromm, Horst Jäger, Matthias Perfahl, and Wolfgang Steinbrecht
Atmos. Chem. Phys., 24, 1997–2021, https://doi.org/10.5194/acp-24-1997-2024, https://doi.org/10.5194/acp-24-1997-2024, 2024
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In 2023, the lidar team at Garmisch-Partenkirchen (Germany) celebrated its 50th year of aerosol profiling. The highlight of these activities has been the lidar measurements of stratospheric aerosol carried out since 1976. The observations since 2017 are characterized by severe smoke from several big fires in North America and Siberia and three volcanic eruptions. The sudden increase in the frequency of such strong fire events is difficult to understand.
Pasquale Sellitto, Redha Belhadji, Juan Cuesta, Aurélien Podglajen, and Bernard Legras
Atmos. Chem. Phys., 23, 15523–15535, https://doi.org/10.5194/acp-23-15523-2023, https://doi.org/10.5194/acp-23-15523-2023, 2023
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Record-breaking wildfires ravaged south-eastern Australia during the fire season 2019–2020. These fires injected a smoke plume in the stratosphere, which dispersed over the whole Southern Hemisphere and interacted with solar and terrestrial radiation. A number of detached smoke bubbles were also observed emanating from this plume and ascending quickly to over 35 km altitude. Here we study how absorption of radiation generated ascending motion of both the the hemispheric plume and the vortices.
Johan Friberg, Bengt G. Martinsson, and Moa K. Sporre
Atmos. Chem. Phys., 23, 12557–12570, https://doi.org/10.5194/acp-23-12557-2023, https://doi.org/10.5194/acp-23-12557-2023, 2023
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We study the short- and long-term stratospheric impact of smoke from the massive Australian wildfires in Dec 2019–Jan 2020 using four satellite sensors. Smoke entered the stratosphere rapidly via transport by firestorms, as well as weeks after the fires. The smoke particle properties evolved over time together with rapidly decreasing stratospheric aerosol load, suggesting photolytic loss of organics in the smoke particles. The depletion rate was estimated to a half-life (e folding) of 10 (14) d.
Larry W. Thomason and Travis Knepp
Atmos. Chem. Phys., 23, 10361–10381, https://doi.org/10.5194/acp-23-10361-2023, https://doi.org/10.5194/acp-23-10361-2023, 2023
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We examine space-based observations of stratospheric aerosol to infer the presence of episodic smoke perturbations. We find that smoke's optical properties often show a consistent behavior but vary somewhat from event to event. We also find that the rate of smoke events observed in the 1984–2005 period is about half the rate of similar observations in the period from 2017 to the present; however, with such low overall rates, inferring change between the periods is difficult.
Felix Wrana, Ulrike Niemeier, Larry W. Thomason, Sandra Wallis, and Christian von Savigny
Atmos. Chem. Phys., 23, 9725–9743, https://doi.org/10.5194/acp-23-9725-2023, https://doi.org/10.5194/acp-23-9725-2023, 2023
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The stratospheric aerosol layer is a naturally occurring and permanent layer of aerosol, in this case very small droplets of mostly sulfuric acid and water, that has a cooling effect on our climate. To quantify this effect and for our general understanding of stratospheric microphysical processes, knowledge of the size of those aerosol particles is needed. Using satellite measurements and atmospheric models we show that some volcanic eruptions can lead to on average smaller aerosol sizes.
Bianca Lauster, Steffen Dörner, Carl-Fredrik Enell, Udo Frieß, Myojeong Gu, Janis Puķīte, Uwe Raffalski, and Thomas Wagner
Atmos. Chem. Phys., 22, 15925–15942, https://doi.org/10.5194/acp-22-15925-2022, https://doi.org/10.5194/acp-22-15925-2022, 2022
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Polar stratospheric clouds (PSCs) are an important component in ozone chemistry. Here, we use two differential optical absorption spectroscopy (DOAS) instruments in the Antarctic and Arctic to investigate the occurrence of PSCs based on the colour index, i.e. the colour of the zenith sky. Additionally using radiative transfer simulations, the variability and the seasonal cycle of PSC occurrence are analysed and an unexpectedly high signal during spring suggests the influence of volcanic aerosol.
Feiyue Mao, Ruixing Shi, Daniel Rosenfeld, Zengxin Pan, Lin Zang, Yannian Zhu, and Xin Lu
Atmos. Chem. Phys., 22, 10589–10602, https://doi.org/10.5194/acp-22-10589-2022, https://doi.org/10.5194/acp-22-10589-2022, 2022
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Previous studies generally ignored the faint aerosols undetected by the CALIPSO layer detection algorithm because they are too optically thin. Here, we retrieved the faint aerosol extinction based on instantaneous CALIPSO observations with the constraint of SAGE data. The correlation and normalized root-mean-square error of the retrievals with independent SAGE data are 0.66 and 100.6 %, respectively. The minimum retrieved extinction at night can be extended to 10-4 km-1 with 125 % uncertainty.
Pasquale Sellitto, Redha Belhadji, Corinna Kloss, and Bernard Legras
Atmos. Chem. Phys., 22, 9299–9311, https://doi.org/10.5194/acp-22-9299-2022, https://doi.org/10.5194/acp-22-9299-2022, 2022
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As a consequence of extreme heat and drought, record-breaking wildfires ravaged south-eastern Australia during the fire season in 2019–2020. Fires injected a smoke plume very high up to the stratosphere, which dispersed quite quickly to the whole Southern Hemisphere and interacted with solar radiation, reflecting and absorbing part of it – thus producing impacts on the climate system. Here we estimate this impact on radiation and we study how it depends on the properties and ageing of the plume.
Kevin Ohneiser, Albert Ansmann, Bernd Kaifler, Alexandra Chudnovsky, Boris Barja, Daniel A. Knopf, Natalie Kaifler, Holger Baars, Patric Seifert, Diego Villanueva, Cristofer Jimenez, Martin Radenz, Ronny Engelmann, Igor Veselovskii, and Félix Zamorano
Atmos. Chem. Phys., 22, 7417–7442, https://doi.org/10.5194/acp-22-7417-2022, https://doi.org/10.5194/acp-22-7417-2022, 2022
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We present and discuss 2 years of long-term lidar observations of the largest stratospheric perturbation by wildfire smoke ever observed. The smoke originated from the record-breaking Australian fires in 2019–2020 and affects climate conditions and even the ozone layer in the Southern Hemisphere. The obvious link between dense smoke occurrence in the stratosphere and strong ozone depletion found in the Arctic and in the Antarctic in 2020 can be regarded as a new aspect of climate change.
Kevin Ohneiser, Albert Ansmann, Alexandra Chudnovsky, Ronny Engelmann, Christoph Ritter, Igor Veselovskii, Holger Baars, Henriette Gebauer, Hannes Griesche, Martin Radenz, Julian Hofer, Dietrich Althausen, Sandro Dahlke, and Marion Maturilli
Atmos. Chem. Phys., 21, 15783–15808, https://doi.org/10.5194/acp-21-15783-2021, https://doi.org/10.5194/acp-21-15783-2021, 2021
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The highlight of the lidar measurements during the 1-year MOSAiC (Multidisciplinary drifting Observatory for the Study of Arctic Climate) expedition of the German icebreaker Polarstern (October 2019–October 2020) was the detection of a persistent, 10 km deep Siberian wildfire smoke layer in the upper troposphere and lower stratosphere (UTLS) from about 7–8 km to 17–18 km height that could potentially have impacted the record-breaking ozone depletion over the Arctic in the spring of 2020.
Elizaveta Malinina, Alexei Rozanov, Ulrike Niemeier, Sandra Wallis, Carlo Arosio, Felix Wrana, Claudia Timmreck, Christian von Savigny, and John P. Burrows
Atmos. Chem. Phys., 21, 14871–14891, https://doi.org/10.5194/acp-21-14871-2021, https://doi.org/10.5194/acp-21-14871-2021, 2021
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In the paper, changes in the stratospheric aerosol loading after the 2018 Ambae eruption were analyzed using OMPS-LP observations. The eruption was also simulated with the MAECHAM5-HAM global climate model. Generally, the model and observations agree very well. We attribute the good consistency of the results to a precisely determined altitude and mass of the volcanic injection, as well as nudging of the meteorological data. The radiative forcing from the eruption was estimated to be −0.13 W m−2.
Albert Ansmann, Kevin Ohneiser, Rodanthi-Elisavet Mamouri, Daniel A. Knopf, Igor Veselovskii, Holger Baars, Ronny Engelmann, Andreas Foth, Cristofer Jimenez, Patric Seifert, and Boris Barja
Atmos. Chem. Phys., 21, 9779–9807, https://doi.org/10.5194/acp-21-9779-2021, https://doi.org/10.5194/acp-21-9779-2021, 2021
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We present retrievals of tropospheric and stratospheric height profiles of particle mass, volume, surface area concentration of wildfire smoke layers, and related cloud condensation nuclei (CCN) and ice-nucleating particle (INP) concentrations. The new analysis scheme is applied to ground-based lidar observations of stratospheric Australian smoke over southern South America and to spaceborne lidar observations of tropospheric North American smoke.
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.
Larry W. Thomason, Mahesh Kovilakam, Anja Schmidt, Christian von Savigny, Travis Knepp, and Landon Rieger
Atmos. Chem. Phys., 21, 1143–1158, https://doi.org/10.5194/acp-21-1143-2021, https://doi.org/10.5194/acp-21-1143-2021, 2021
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Measurements of the impact of volcanic eruptions on stratospheric aerosol loading by space-based instruments show show a fairly well-behaved relationship between the magnitude and the apparent changes to aerosol size over several orders of magnitude. This directly measured relationship provides a unique opportunity to verify the performance of interactive aerosol models used in climate models.
Corinna Kloss, Gwenaël Berthet, Pasquale Sellitto, Felix Ploeger, Ghassan Taha, Mariam Tidiga, Maxim Eremenko, Adriana Bossolasco, Fabrice Jégou, Jean-Baptiste Renard, and Bernard Legras
Atmos. Chem. Phys., 21, 535–560, https://doi.org/10.5194/acp-21-535-2021, https://doi.org/10.5194/acp-21-535-2021, 2021
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The year 2019 was particularly rich for the stratospheric aerosol layer due to two volcanic eruptions (at Raikoke and Ulawun) and wildfire events. With satellite observations and models, we describe the exceptionally complex situation following the Raikoke eruption. The respective plume overwhelmed the Northern Hemisphere stratosphere in terms of aerosol load and resulted in the highest climate impact throughout the past decade.
Anna Gialitaki, Alexandra Tsekeri, Vassilis Amiridis, Romain Ceolato, Lucas Paulien, Anna Kampouri, Antonis Gkikas, Stavros Solomos, Eleni Marinou, Moritz Haarig, Holger Baars, Albert Ansmann, Tatyana Lapyonok, Anton Lopatin, Oleg Dubovik, Silke Groß, Martin Wirth, Maria Tsichla, Ioanna Tsikoudi, and Dimitris Balis
Atmos. Chem. Phys., 20, 14005–14021, https://doi.org/10.5194/acp-20-14005-2020, https://doi.org/10.5194/acp-20-14005-2020, 2020
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Stratospheric smoke particles are found to significantly depolarize incident light, while this effect is also accompanied by a strong spectral dependence. We utilize scattering simulations to show that this behaviour can be attributed to the near-spherical shape of the particles. We also examine whether an extension of the current AERONET scattering model to include the near-spherical shapes could be of benefit to the AERONET retrieval for stratospheric smoke associated with enhanced PLDR.
Kevin Ohneiser, Albert Ansmann, Holger Baars, Patric Seifert, Boris Barja, Cristofer Jimenez, Martin Radenz, Audrey Teisseire, Athina Floutsi, Moritz Haarig, Andreas Foth, Alexandra Chudnovsky, Ronny Engelmann, Félix Zamorano, Johannes Bühl, and Ulla Wandinger
Atmos. Chem. Phys., 20, 8003–8015, https://doi.org/10.5194/acp-20-8003-2020, https://doi.org/10.5194/acp-20-8003-2020, 2020
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Unique lidar observations of a strong perturbation in stratospheric aerosol conditions in the Southern Hemisphere caused by the extreme Australian bushfires in 2019–2020 are presented. One of the main goals of this article is to provide the CALIPSO and Aeolus spaceborne lidar science teams with basic input parameters (lidar ratios, depolarization ratios) for a trustworthy documentation of this record-breaking event.
Fernando Chouza, Thierry Leblanc, John Barnes, Mark Brewer, Patrick Wang, and Darryl Koon
Atmos. Chem. Phys., 20, 6821–6839, https://doi.org/10.5194/acp-20-6821-2020, https://doi.org/10.5194/acp-20-6821-2020, 2020
Holger Baars, Albert Ansmann, Kevin Ohneiser, Moritz Haarig, Ronny Engelmann, Dietrich Althausen, Ingrid Hanssen, Michael Gausa, Aleksander Pietruczuk, Artur Szkop, Iwona S. Stachlewska, Dongxiang Wang, Jens Reichardt, Annett Skupin, Ina Mattis, Thomas Trickl, Hannes Vogelmann, Francisco Navas-Guzmán, Alexander Haefele, Karen Acheson, Albert A. Ruth, Boyan Tatarov, Detlef Müller, Qiaoyun Hu, Thierry Podvin, Philippe Goloub, Igor Veselovskii, Christophe Pietras, Martial Haeffelin, Patrick Fréville, Michaël Sicard, Adolfo Comerón, Alfonso Javier Fernández García, Francisco Molero Menéndez, Carmen Córdoba-Jabonero, Juan Luis Guerrero-Rascado, Lucas Alados-Arboledas, Daniele Bortoli, Maria João Costa, Davide Dionisi, Gian Luigi Liberti, Xuan Wang, Alessia Sannino, Nikolaos Papagiannopoulos, Antonella Boselli, Lucia Mona, Giuseppe D'Amico, Salvatore Romano, Maria Rita Perrone, Livio Belegante, Doina Nicolae, Ivan Grigorov, Anna Gialitaki, Vassilis Amiridis, Ourania Soupiona, Alexandros Papayannis, Rodanthi-Elisaveth Mamouri, Argyro Nisantzi, Birgit Heese, Julian Hofer, Yoav Y. Schechner, Ulla Wandinger, and Gelsomina Pappalardo
Atmos. Chem. Phys., 19, 15183–15198, https://doi.org/10.5194/acp-19-15183-2019, https://doi.org/10.5194/acp-19-15183-2019, 2019
Corinna Kloss, Gwenaël Berthet, Pasquale Sellitto, Felix Ploeger, Silvia Bucci, Sergey Khaykin, Fabrice Jégou, Ghassan Taha, Larry W. Thomason, Brice Barret, Eric Le Flochmoen, Marc von Hobe, Adriana Bossolasco, Nelson Bègue, and Bernard Legras
Atmos. Chem. Phys., 19, 13547–13567, https://doi.org/10.5194/acp-19-13547-2019, https://doi.org/10.5194/acp-19-13547-2019, 2019
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With satellite measurements and transport models, we show that a plume resulting from strong Canadian fires in July/August 2017 was not only distributed throughout the northern/higher latitudes, but also reached the faraway tropics, aided by the circulation of Asian monsoon anticyclone. The regional climate impact in the wider Asian monsoon area in September exceeds the impact of the Asian tropopause aerosol layer by a factor of ~ 3 and compares to that of an advected moderate volcanic eruption.
Vladimir V. Zuev, Vladislav V. Gerasimov, Aleksei V. Nevzorov, and Ekaterina S. Savelieva
Atmos. Chem. Phys., 19, 3341–3356, https://doi.org/10.5194/acp-19-3341-2019, https://doi.org/10.5194/acp-19-3341-2019, 2019
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Massive wildfires sometimes generate pyrocumulonimbus clouds (pyroCbs), inside of which combustion products can ascend to the upper troposphere or even lower stratosphere (UTLS). Smoke plumes from pyroCbs occurred in North America can spread in the UTLS for long distances and be observed in the UTLS over Europe and even over Russia. In this work, we analyzed aerosol layers detected in the UTLS over Tomsk (Russia) that could be smoke plumes from such pyroCbs that occurred in the 2000–2017 period.
Qiaoyun Hu, Philippe Goloub, Igor Veselovskii, Juan-Antonio Bravo-Aranda, Ioana Elisabeta Popovici, Thierry Podvin, Martial Haeffelin, Anton Lopatin, Oleg Dubovik, Christophe Pietras, Xin Huang, Benjamin Torres, and Cheng Chen
Atmos. Chem. Phys., 19, 1173–1193, https://doi.org/10.5194/acp-19-1173-2019, https://doi.org/10.5194/acp-19-1173-2019, 2019
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Smoke plumes generated in Canadian fire activities were elevated to the lower stratosphere and transported from North America to Europe. The smoke plumes were observed by three lidar systems in northern France. This study provides a comprehensive characterization for aged smoke aerosols at high altitude using lidar observations. It presents that fire activities on the Earth's surface can be an important contributor of stratospheric aerosols and impact the Earth's radiation budget.
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.
Albert Ansmann, Holger Baars, Alexandra Chudnovsky, Ina Mattis, Igor Veselovskii, Moritz Haarig, Patric Seifert, Ronny Engelmann, and Ulla Wandinger
Atmos. Chem. Phys., 18, 11831–11845, https://doi.org/10.5194/acp-18-11831-2018, https://doi.org/10.5194/acp-18-11831-2018, 2018
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Extremely large light extinction coefficients of 500 Mm-1, about 20 times higher than after the Pinatubo volcanic eruptions in 1991, were observed by EARLINET lidars in the stratosphere over central Europe from 21 to 22 August, 2017. This paper provides an overview based on ground-based (lidar, AERONET) and satellite (MODIS, OMI) remote sensing.
Moritz Haarig, Albert Ansmann, Holger Baars, Cristofer Jimenez, Igor Veselovskii, Ronny Engelmann, and Dietrich Althausen
Atmos. Chem. Phys., 18, 11847–11861, https://doi.org/10.5194/acp-18-11847-2018, https://doi.org/10.5194/acp-18-11847-2018, 2018
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The worldwide only triple-wavelength polarization/Raman lidar was used to measure optical, microphysical, and morphological properties of aged Canadian wildfire smoke occurring in the troposphere and stratosphere over Leipzig, Germany, in August 2017. A strong contrast between the tropospheric and stratospheric smoke properties was found.
Johan Friberg, Bengt G. Martinsson, Sandra M. Andersson, and Oscar S. Sandvik
Atmos. Chem. Phys., 18, 11149–11169, https://doi.org/10.5194/acp-18-11149-2018, https://doi.org/10.5194/acp-18-11149-2018, 2018
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During 2006–2015 volcanism contributed 40 % of the stratospheric aerosol load. We compute the AOD (aerosol optical depth) of the stratosphere (from the tropopause to 35 km altitude) using new techniques of handling CALIOP data. Regional and global AODs are presented for the entire stratosphere in relation to transport patterns, and the AOD is presented for three stratospheric layers: the LMS, the potential temperature range of 380 to 470 K, and altitudes above the 470 K isentrope.
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.
Alyn Lambert and Michelle L. Santee
Atmos. Chem. Phys., 18, 1945–1975, https://doi.org/10.5194/acp-18-1945-2018, https://doi.org/10.5194/acp-18-1945-2018, 2018
Andrew T. Prata, Stuart A. Young, Steven T. Siems, and Michael J. Manton
Atmos. Chem. Phys., 17, 8599–8618, https://doi.org/10.5194/acp-17-8599-2017, https://doi.org/10.5194/acp-17-8599-2017, 2017
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We have studied the optical properties of ash-rich and sulfate-rich volcanic aerosols by analysing satellite observations of three different volcanic eruptions. Our results indicate that ash particles have distinctive optical properties when compared to sulfates. We expect our results will improve space-borne lidar detection of volcanic aerosols and provide new insight into their interaction with the atmosphere and solar radiation.
Vladimir V. Zuev, Vladimir D. Burlakov, Aleksei V. Nevzorov, Vladimir L. Pravdin, Ekaterina S. Savelieva, and Vladislav V. Gerasimov
Atmos. Chem. Phys., 17, 3067–3081, https://doi.org/10.5194/acp-17-3067-2017, https://doi.org/10.5194/acp-17-3067-2017, 2017
Sergey M. Khaykin, Sophie Godin-Beekmann, Philippe Keckhut, Alain Hauchecorne, Julien Jumelet, Jean-Paul Vernier, Adam Bourassa, Doug A. Degenstein, Landon A. Rieger, Christine Bingen, Filip Vanhellemont, Charles Robert, Matthew DeLand, and Pawan K. Bhartia
Atmos. Chem. Phys., 17, 1829–1845, https://doi.org/10.5194/acp-17-1829-2017, https://doi.org/10.5194/acp-17-1829-2017, 2017
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The article is devoted to the long-term evolution and variability of stratospheric aerosol, which plays an important role in climate change and the ozone layer. We use 22-year long continuous observations using laser radar soundings in southern France and satellite-based observations to distinguish between natural aerosol variability (caused by volcanic eruptions) and human-induced change in aerosol concentration. An influence of growing pollution above Asia on stratospheric aerosol is found.
Alyn Lambert, Michelle L. Santee, and Nathaniel J. Livesey
Atmos. Chem. Phys., 16, 15219–15246, https://doi.org/10.5194/acp-16-15219-2016, https://doi.org/10.5194/acp-16-15219-2016, 2016
Wolfgang Woiwode, Michael Höpfner, Lei Bi, Michael C. Pitts, Lamont R. Poole, Hermann Oelhaf, Sergej Molleker, Stephan Borrmann, Marcus Klingebiel, Gennady Belyaev, Andreas Ebersoldt, Sabine Griessbach, Jens-Uwe Grooß, Thomas Gulde, Martina Krämer, Guido Maucher, Christof Piesch, Christian Rolf, Christian Sartorius, Reinhold Spang, and Johannes Orphal
Atmos. Chem. Phys., 16, 9505–9532, https://doi.org/10.5194/acp-16-9505-2016, https://doi.org/10.5194/acp-16-9505-2016, 2016
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The analysis of spectral signatures of a polar stratospheric cloud in airborne infrared remote sensing observations in the Arctic in combination with further collocated measurements supports the view that the observed cloud consisted of highly aspherical nitric acid trihydrate particles. A characteristic "shoulder-like" spectral signature may be exploited for identification of large, highly aspherical nitric acid trihydrate particles involved in denitrification of the polar winter stratosphere.
T. Grigas, M. Hervo, G. Gimmestad, H. Forrister, P. Schneider, J. Preißler, L. Tarrason, and C. O'Dowd
Atmos. Chem. Phys., 15, 12179–12191, https://doi.org/10.5194/acp-15-12179-2015, https://doi.org/10.5194/acp-15-12179-2015, 2015
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The expedited near-real-time Level 1.5 Cloud-Aerosol Lidar with Orthogonal Polarization version 3 products were evaluated against data from the ground-based European Aerosol Research Lidar Network. The statistical framework and results of the 3-year evaluation of 48 CALIOP overpasses with ground tracks within a 100km distance from operating EARLINET stations are presented.
M. J. M. Penning de Vries, S. Dörner, J. Puķīte, C. Hörmann, M. D. Fromm, and T. Wagner
Atmos. Chem. Phys., 14, 8149–8163, https://doi.org/10.5194/acp-14-8149-2014, https://doi.org/10.5194/acp-14-8149-2014, 2014
T. D. Fairlie, J.-P. Vernier, M. Natarajan, and K. M. Bedka
Atmos. Chem. Phys., 14, 7045–7057, https://doi.org/10.5194/acp-14-7045-2014, https://doi.org/10.5194/acp-14-7045-2014, 2014
I. A. Mironova and I. G. Usoskin
Atmos. Chem. Phys., 13, 8543–8550, https://doi.org/10.5194/acp-13-8543-2013, https://doi.org/10.5194/acp-13-8543-2013, 2013
M. C. Pitts, L. R. Poole, A. Lambert, and L. W. Thomason
Atmos. Chem. Phys., 13, 2975–2988, https://doi.org/10.5194/acp-13-2975-2013, https://doi.org/10.5194/acp-13-2975-2013, 2013
O. Uchino, T. Sakai, T. Nagai, K. Nakamae, I. Morino, K. Arai, H. Okumura, S. Takubo, T. Kawasaki, Y. Mano, T. Matsunaga, and T. Yokota
Atmos. Chem. Phys., 12, 11975–11984, https://doi.org/10.5194/acp-12-11975-2012, https://doi.org/10.5194/acp-12-11975-2012, 2012
L. W. Thomason
Atmos. Chem. Phys., 12, 8177–8188, https://doi.org/10.5194/acp-12-8177-2012, https://doi.org/10.5194/acp-12-8177-2012, 2012
I. A. Mironova, I. G. Usoskin, G. A. Kovaltsov, and S. V. Petelina
Atmos. Chem. Phys., 12, 769–778, https://doi.org/10.5194/acp-12-769-2012, https://doi.org/10.5194/acp-12-769-2012, 2012
A. E. Bourassa, L. A. Rieger, N. D. Lloyd, and D. A. Degenstein
Atmos. Chem. Phys., 12, 605–614, https://doi.org/10.5194/acp-12-605-2012, https://doi.org/10.5194/acp-12-605-2012, 2012
F. Vanhellemont, D. Fussen, N. Mateshvili, C. Tétard, C. Bingen, E. Dekemper, N. Loodts, E. Kyrölä, V. Sofieva, J. Tamminen, A. Hauchecorne, J.-L. Bertaux, F. Dalaudier, L. Blanot, O. Fanton d'Andon, G. Barrot, M. Guirlet, T. Fehr, and L. Saavedra
Atmos. Chem. Phys., 10, 7997–8009, https://doi.org/10.5194/acp-10-7997-2010, https://doi.org/10.5194/acp-10-7997-2010, 2010
D. Wurl, R. G. Grainger, A. J. McDonald, and T. Deshler
Atmos. Chem. Phys., 10, 4295–4317, https://doi.org/10.5194/acp-10-4295-2010, https://doi.org/10.5194/acp-10-4295-2010, 2010
C. David, P. Keckhut, A. Armetta, J. Jumelet, M. Snels, M. Marchand, and S. Bekki
Atmos. Chem. Phys., 10, 3813–3825, https://doi.org/10.5194/acp-10-3813-2010, https://doi.org/10.5194/acp-10-3813-2010, 2010
L. W. Thomason, J. R. Moore, M. C. Pitts, J. M. Zawodny, and E. W. Chiou
Atmos. Chem. Phys., 10, 2159–2173, https://doi.org/10.5194/acp-10-2159-2010, https://doi.org/10.5194/acp-10-2159-2010, 2010
Cited articles
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Short summary
Large amounts of wildfire smoke reached the stratosphere in 2017. The literature on stratospheric aerosol is mainly based on horizontally viewing sensors that saturate in dense smoke. Using also a vertically viewing sensor with orders of magnitude shorter path in the smoke, we show that the horizontally viewing sensors miss a dramatic exponential decline of the aerosol load with a half-life of 10 d, where 80 %–90 % of smoke is lost. We attribute the decline to photolytic loss of organic aerosol.
Large amounts of wildfire smoke reached the stratosphere in 2017. The literature on...
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