Articles | Volume 21, issue 10
https://doi.org/10.5194/acp-21-7881-2021
© Author(s) 2021. 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-21-7881-2021
© Author(s) 2021. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
GUV long-term measurements of total ozone column and effective cloud transmittance at three Norwegian sites
NILU – Norwegian Institute for Air Research, Kjeller, Norway
Bjørn Johnsen
Norwegian Radiation and Nuclear Safety Authority, Østerås, Norway
Arve Kylling
NILU – Norwegian Institute for Air Research, Kjeller, Norway
Arne Dahlback
Department of Physics, University of Oslo, Oslo, Norway
Germar H. Bernhard
Biospherical Instruments Inc., San Diego, CA, USA
Georg H. Hansen
NILU – Norwegian Institute for Air Research, Kjeller, Norway
Boyan Petkov
Department of Psychological Sciences, Health and Territory, D'Annunzio University, Chieti, Italy
National Research Council, Institute of Polar Sciences (CNR-ISP),
Bologna, Italy
Vito Vitale
National Research Council, Institute of Polar Sciences (CNR-ISP),
Bologna, Italy
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Aki Virkkula, Henrik Grythe, John Backman, Tuukka Petäjä, Maurizio Busetto, Christian Lanconelli, Angelo Lupi, Silvia Becagli, Rita Traversi, Mirko Severi, Vito Vitale, Patrick Sheridan, and Elisabeth Andrews
Atmos. Chem. Phys., 22, 5033–5069, https://doi.org/10.5194/acp-22-5033-2022, https://doi.org/10.5194/acp-22-5033-2022, 2022
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Christine D. Groot Zwaaftink, Wenche Aas, Sabine Eckhardt, Nikolaos Evangeliou, Paul Hamer, Mona Johnsrud, Arve Kylling, Stephen M. Platt, Kerstin Stebel, Hilde Uggerud, and Karl Espen Yttri
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Claudia Emde, Huan Yu, Arve Kylling, Michel van Roozendael, Kerstin Stebel, Ben Veihelmann, and Bernhard Mayer
Atmos. Meas. Tech., 15, 1587–1608, https://doi.org/10.5194/amt-15-1587-2022, https://doi.org/10.5194/amt-15-1587-2022, 2022
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Stephen M. Platt, Øystein Hov, Torunn Berg, Knut Breivik, Sabine Eckhardt, Konstantinos Eleftheriadis, Nikolaos Evangeliou, Markus Fiebig, Rebecca Fisher, Georg Hansen, Hans-Christen Hansson, Jost Heintzenberg, Ove Hermansen, Dominic Heslin-Rees, Kim Holmén, Stephen Hudson, Roland Kallenborn, Radovan Krejci, Terje Krognes, Steinar Larssen, David Lowry, Cathrine Lund Myhre, Chris Lunder, Euan Nisbet, Pernilla B. Nizzetto, Ki-Tae Park, Christina A. Pedersen, Katrine Aspmo Pfaffhuber, Thomas Röckmann, Norbert Schmidbauer, Sverre Solberg, Andreas Stohl, Johan Ström, Tove Svendby, Peter Tunved, Kjersti Tørnkvist, Carina van der Veen, Stergios Vratolis, Young Jun Yoon, Karl Espen Yttri, Paul Zieger, Wenche Aas, and Kjetil Tørseth
Atmos. Chem. Phys., 22, 3321–3369, https://doi.org/10.5194/acp-22-3321-2022, https://doi.org/10.5194/acp-22-3321-2022, 2022
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Panagiotis G. Kosmopoulos, Stelios Kazadzis, Alois W. Schmalwieser, Panagiotis I. Raptis, Kyriakoula Papachristopoulou, Ilias Fountoulakis, Akriti Masoom, Alkiviadis F. Bais, Julia Bilbao, Mario Blumthaler, Axel Kreuter, Anna Maria Siani, Kostas Eleftheratos, Chrysanthi Topaloglou, Julian Gröbner, Bjørn Johnsen, Tove M. Svendby, Jose Manuel Vilaplana, Lionel Doppler, Ann R. Webb, Marina Khazova, Hugo De Backer, Anu Heikkilä, Kaisa Lakkala, Janusz Jaroslawski, Charikleia Meleti, Henri Diémoz, Gregor Hülsen, Barbara Klotz, John Rimmer, and Charalampos Kontoes
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Atmos. Meas. Tech., 14, 481–510, https://doi.org/10.5194/amt-14-481-2021, https://doi.org/10.5194/amt-14-481-2021, 2021
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This paper reports on the ground-based validation of the NO2 data produced operationally by the TROPOMI instrument on board the Sentinel-5 Precursor satellite. Tropospheric, stratospheric, and total NO2 columns are compared to measurements collected from MAX-DOAS, ZSL-DOAS, and PGN/Pandora instruments respectively. The products are found to satisfy mission requirements in general, though negative mean differences are found at sites with high pollution levels. Potential causes are discussed.
Kaisa Lakkala, Jukka Kujanpää, Colette Brogniez, Nicolas Henriot, Antti Arola, Margit Aun, Frédérique Auriol, Alkiviadis F. Bais, Germar Bernhard, Veerle De Bock, Maxime Catalfamo, Christine Deroo, Henri Diémoz, Luca Egli, Jean-Baptiste Forestier, Ilias Fountoulakis, Katerina Garane, Rosa Delia Garcia, Julian Gröbner, Seppo Hassinen, Anu Heikkilä, Stuart Henderson, Gregor Hülsen, Bjørn Johnsen, Niilo Kalakoski, Angelos Karanikolas, Tomi Karppinen, Kevin Lamy, Sergio F. León-Luis, Anders V. Lindfors, Jean-Marc Metzger, Fanny Minvielle, Harel B. Muskatel, Thierry Portafaix, Alberto Redondas, Ricardo Sanchez, Anna Maria Siani, Tove Svendby, and Johanna Tamminen
Atmos. Meas. Tech., 13, 6999–7024, https://doi.org/10.5194/amt-13-6999-2020, https://doi.org/10.5194/amt-13-6999-2020, 2020
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The TROPOspheric Monitoring Instrument (TROPOMI) onboard the Sentinel-5 Precursor (S5P) satellite was launched on 13 October 2017 to provide the atmospheric composition for atmosphere and climate research. Ground-based data from 25 sites located in Arctic, subarctic, temperate, equatorial and Antarctic
areas were used for the validation of the TROPOMI surface ultraviolet (UV) radiation product. For most sites 60 %–80 % of TROPOMI data was within ± 20 % of ground-based data.
Arantxa M. Triana-Gómez, Georg Heygster, Christian Melsheimer, Gunnar Spreen, Monia Negusini, and Boyan H. Petkov
Atmos. Meas. Tech., 13, 3697–3715, https://doi.org/10.5194/amt-13-3697-2020, https://doi.org/10.5194/amt-13-3697-2020, 2020
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In the Arctic, in situ measurements are sparse and standard remote sensing retrieval methods have problems. We present advances in a retrieval algorithm for vertically integrated water vapour tuned for polar regions. In addition to the initial sensor used (AMSU-B), we can now also use data from the successor instrument (MHS). Additionally, certain artefacts are now filtered out. Comparison with radiosondes shows the overall good performance of the updated algorithm.
Arve Kylling, Hamidreza Ardeshiri, Massimo Cassiani, Anna Solvejg Dinger, Soon-Young Park, Ignacio Pisso, Norbert Schmidbauer, Kerstin Stebel, and Andreas Stohl
Atmos. Meas. Tech., 13, 3303–3318, https://doi.org/10.5194/amt-13-3303-2020, https://doi.org/10.5194/amt-13-3303-2020, 2020
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Atmospheric turbulence and its effect on tracer dispersion in particular may be measured by cameras sensitive to the absorption of ultraviolet (UV) sunlight by sulfur dioxide (SO2). Using large eddy simulation and 3D Monte Carlo radiative transfer modelling of a SO2 plume, we demonstrate that UV camera images of SO2 plumes may be used to derive plume statistics of relevance for the study of atmospheric turbulent dispersion.
Margit Aun, Kaisa Lakkala, Ricardo Sanchez, Eija Asmi, Fernando Nollas, Outi Meinander, Larisa Sogacheva, Veerle De Bock, Antti Arola, Gerrit de Leeuw, Veijo Aaltonen, David Bolsée, Klara Cizkova, Alexander Mangold, Ladislav Metelka, Erko Jakobson, Tove Svendby, Didier Gillotay, and Bert Van Opstal
Atmos. Chem. Phys., 20, 6037–6054, https://doi.org/10.5194/acp-20-6037-2020, https://doi.org/10.5194/acp-20-6037-2020, 2020
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In 2017, new measurements of UV radiation started in Marambio, Antarctica, by the Finnish Meteorological Institute in collaboration with the Argentinian Servicio Meteorológico Nacional. The paper presents the results of UV irradiance measurements from March 2017 to March 2019, and it
compares them with those from 2000–2008 and also with UV measurements at other Antarctic stations. In 2017/2018, below average UV radiation levels were recorded due to favourable ozone and cloud conditions.
Kaisa Lakkala, Margit Aun, Ricardo Sanchez, Germar Bernhard, Eija Asmi, Outi Meinander, Fernando Nollas, Gregor Hülsen, Tomi Karppinen, Veijo Aaltonen, Antti Arola, and Gerrit de Leeuw
Earth Syst. Sci. Data, 12, 947–960, https://doi.org/10.5194/essd-12-947-2020, https://doi.org/10.5194/essd-12-947-2020, 2020
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A GUV multi-filter radiometer was set up at Marambio, 64° S, 56° W, Antarctica, in 2017. The instrument continuously measures ultraviolet (UV) radiation, visible (VIS) radiation and photosynthetically active radiation (PAR). The measurements are designed for providing high-quality long-term time series that can be used to assess the impact of global climate change in the Antarctic region. The data from the last 5 d are plotted and updated daily.
Paul Ockenfuß, Claudia Emde, Bernhard Mayer, and Germar Bernhard
Atmos. Chem. Phys., 20, 1961–1976, https://doi.org/10.5194/acp-20-1961-2020, https://doi.org/10.5194/acp-20-1961-2020, 2020
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We model solar radiation as it would be measured on the Earth's surface in the core shadow of a total solar eclipse. Subsequently, we compare our results to observations during the total eclipse 2017 for ultraviolet, visible and near-infrared wavelengths. Moreover, we analyze the effect of the surface reflectance, the ozone profile, aerosol and the topography and give a visualization of the prevailing photons paths in the atmosphere during the eclipse.
Sieglinde Callewaert, Sophie Vandenbussche, Nicolas Kumps, Arve Kylling, Xiaoxia Shang, Mika Komppula, Philippe Goloub, and Martine De Mazière
Atmos. Meas. Tech., 12, 3673–3698, https://doi.org/10.5194/amt-12-3673-2019, https://doi.org/10.5194/amt-12-3673-2019, 2019
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This article presents the updated MAPIR algorithm, which uses infrared satellite data to obtain the global 3-D distribution of mineral aerosols. A description of the method together with its technical improvements is given. Additionally, a 10-year data set was generated and used to evaluate this new algorithm against AERONET, CALIOP, CATS and two ground-based lidar stations. We have shown that the new MAPIR algorithm provides reliable aerosol optical depth and dust layer mean altitude profiles.
Germar Bernhard and Boyan Petkov
Atmos. Chem. Phys., 19, 4703–4719, https://doi.org/10.5194/acp-19-4703-2019, https://doi.org/10.5194/acp-19-4703-2019, 2019
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Solar radiation at ultraviolet, visible, and infrared wavelengths was measured during the total solar eclipse of 21 August 2017. Data were used to study the wavelength-dependent changes of solar radiation at Earth’s surface and to validate parameterizations of solar limb darkening (LD), which describes the change in the Sun’s brightness between its center and its edge. The study highlights the importance of the LD effect when calculating total ozone and aerosol optical depth during an eclipse.
Nikolaos Evangeliou, Arve Kylling, Sabine Eckhardt, Viktor Myroniuk, Kerstin Stebel, Ronan Paugam, Sergiy Zibtsev, and Andreas Stohl
Atmos. Chem. Phys., 19, 1393–1411, https://doi.org/10.5194/acp-19-1393-2019, https://doi.org/10.5194/acp-19-1393-2019, 2019
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We simulated the peatland fires that burned in Greenland in summer 2017. Using satellite data, we estimated that the total burned area was 2345 ha, the fuel amount consumed 117 kt C and the emissions of BC, OC and BrC 23.5, 731 and 141 t, respectively. About 30 % of the emissions were deposited on snow or ice surfaces. This caused a maximum albedo change of 0.007 and a surface radiative forcing of 0.03–0.04 W m−2, with local maxima of up to 0.63–0.77 W m−2. Overall, the fires had a small impact.
Stephen M. Platt, Sabine Eckhardt, Benedicte Ferré, Rebecca E. Fisher, Ove Hermansen, Pär Jansson, David Lowry, Euan G. Nisbet, Ignacio Pisso, Norbert Schmidbauer, Anna Silyakova, Andreas Stohl, Tove M. Svendby, Sunil Vadakkepuliyambatta, Jürgen Mienert, and Cathrine Lund Myhre
Atmos. Chem. Phys., 18, 17207–17224, https://doi.org/10.5194/acp-18-17207-2018, https://doi.org/10.5194/acp-18-17207-2018, 2018
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We measured atmospheric mixing ratios of methane over the Arctic Ocean around Svalbard and compared observed variations to inventories for anthropogenic, wetland, and biomass burning methane emissions and an atmospheric transport model. With knowledge of where variations were expected due to the aforementioned land-based emissions, we were able to identify and quantify a methane source from the ocean north of Svalbard, likely from sub-sea hydrocarbon seeps and/or gas hydrate decomposition.
Anna Solvejg Dinger, Kerstin Stebel, Massimo Cassiani, Hamidreza Ardeshiri, Cirilo Bernardo, Arve Kylling, Soon-Young Park, Ignacio Pisso, Norbert Schmidbauer, Jan Wasseng, and Andreas Stohl
Atmos. Meas. Tech., 11, 6169–6188, https://doi.org/10.5194/amt-11-6169-2018, https://doi.org/10.5194/amt-11-6169-2018, 2018
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This study presents an artificial release experiment aimed to improve the understanding of turbulence in the atmospheric boundary layer. A new set of image processing methods was developed to analyse the turbulent dispersion of sulfur dioxide (SO2) puffs. For this a tomographic setup of six SO2 cameras was used to image artificially released SO2 gas.
Kaisa Lakkala, Alberto Redondas, Outi Meinander, Laura Thölix, Britta Hamari, Antonio Fernando Almansa, Virgilio Carreno, Rosa Delia García, Carlos Torres, Guillermo Deferrari, Hector Ochoa, Germar Bernhard, Ricardo Sanchez, and Gerrit de Leeuw
Atmos. Chem. Phys., 18, 16019–16031, https://doi.org/10.5194/acp-18-16019-2018, https://doi.org/10.5194/acp-18-16019-2018, 2018
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Solar UV irradiances were measured at Ushuaia (54° S) and Marambio (64° S) during 2000–2013. The measurements were part of the Antarctic NILU-UV network, which was maintained as a cooperation between Spain, Argentina and Finland. The time series of the network were analysed for the first time in this study. At both stations maximum UV indices and daily doses were measured when spring-time ozone loss episodes occurred. The maximum UV index was 13 and 12 in Ushuaia and Marambio, respectively.
Arve Kylling, Sophie Vandenbussche, Virginie Capelle, Juan Cuesta, Lars Klüser, Luca Lelli, Thomas Popp, Kerstin Stebel, and Pepijn Veefkind
Atmos. Meas. Tech., 11, 2911–2936, https://doi.org/10.5194/amt-11-2911-2018, https://doi.org/10.5194/amt-11-2911-2018, 2018
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The aerosol layer height is one of four aerosol parameters which is needed to enhance our understanding of aerosols' role in the climate system. Both active and passive measurement methods may be used to estimate the aerosol layer height. Aerosol height estimates made from passive infrared and solar satellite sensors measurements are compared with satellite-borne lidar estimates. There is considerable variation between the retrieved dust heights and how they compare with the lidar.
Martine De Mazière, Anne M. Thompson, Michael J. Kurylo, Jeannette D. Wild, Germar Bernhard, Thomas Blumenstock, Geir O. Braathen, James W. Hannigan, Jean-Christopher Lambert, Thierry Leblanc, Thomas J. McGee, Gerald Nedoluha, Irina Petropavlovskikh, Gunther Seckmeyer, Paul C. Simon, Wolfgang Steinbrecht, and Susan E. Strahan
Atmos. Chem. Phys., 18, 4935–4964, https://doi.org/10.5194/acp-18-4935-2018, https://doi.org/10.5194/acp-18-4935-2018, 2018
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This paper serves as an introduction to the special issue "Twenty-five years of operations of the Network for the Detection of Atmospheric Composition Change (NDACC)". It describes the origins of the network, its actual status, and some perspectives for its future evolution in the context of atmospheric sciences.
Jonas Gliß, Kerstin Stebel, Arve Kylling, and Aasmund Sudbø
Atmos. Meas. Tech., 11, 781–801, https://doi.org/10.5194/amt-11-781-2018, https://doi.org/10.5194/amt-11-781-2018, 2018
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The paper focusses on gas-velocity retrievals in emission plumes using optical flow (OF) algorithms applied to remote sensing imagery. OF algorithms can measure the velocities on a pixel level between consecutive images. An issue of OF algorithms is that they often fail to detect motion in contrast-poor image areas. A correction based on histograms of an OF vector field is proposed. The new method is applied to two example volcanic data sets from Mt Etna, Italy and Guallatiri, Chile.
Germar Bernhard, Irina Petropavlovskikh, and Bernhard Mayer
Atmos. Meas. Tech., 10, 4979–4994, https://doi.org/10.5194/amt-10-4979-2017, https://doi.org/10.5194/amt-10-4979-2017, 2017
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The vertical distribution of atmospheric ozone has historically been measured from the ground by analysing the wavelength dependence of zenith radiation. Our method retrieves the same information from global irradiance, which is defined as radiant flux received from the entire upper hemisphere, including the Sun. The new method makes existing long-term data sets of global irradiance available for studying ozone profiles. The accuracy of the new method is similar to that of the legacy method.
William Wandji Nyamsi, Mikko R. A. Pitkänen, Youva Aoun, Philippe Blanc, Anu Heikkilä, Kaisa Lakkala, Germar Bernhard, Tapani Koskela, Anders V. Lindfors, Antti Arola, and Lucien Wald
Atmos. Meas. Tech., 10, 4965–4978, https://doi.org/10.5194/amt-10-4965-2017, https://doi.org/10.5194/amt-10-4965-2017, 2017
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This paper proposes a new, fast and accurate method for estimating UV fluxes at ground level in cloud-free conditions at any place and time. The method performs very well with the Copernicus Atmosphere Monitoring Service products as inputs describing the state of the atmosphere. An accuracy that is close to the uncertainty of the measurements themselves is reached. We believe that our research will be widely used in the near future.
Birthe Marie Steensen, Arve Kylling, Nina Iren Kristiansen, and Michael Schulz
Atmos. Chem. Phys., 17, 9205–9222, https://doi.org/10.5194/acp-17-9205-2017, https://doi.org/10.5194/acp-17-9205-2017, 2017
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An inversion method is tested in a forecasting setting for constraining ash dispersion by satellite observations. The sensitivity of a priori and
satellite uncertainties is tested for the a posteriori term. The a posteriori is also tested with four different assumptions affecting the retrieved
ash satellite data. In forecasting mode, the a posteriori changes after only 12 h of satellite observations and produces better forecasts than a priori.
John Faulkner Burkhart, Arve Kylling, Crystal B. Schaaf, Zhuosen Wang, Wiley Bogren, Rune Storvold, Stian Solbø, Christina A. Pedersen, and Sebastian Gerland
The Cryosphere, 11, 1575–1589, https://doi.org/10.5194/tc-11-1575-2017, https://doi.org/10.5194/tc-11-1575-2017, 2017
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We present the first use of spectrometer measurements from a drone to assess reflectance and albedo over the Greenland Ice Sheet. In order to measure albedo – a critical parameter in the earth's energy balance – a drone was flown along 200 km transects coincident with Terra and Aqua satellites flying MODIS. We present a direct comparison of UAV-measured reflectance with satellite data over Greenland and provide a new method to study cryospheric surfaces using UAV with spectral instruments.
Frances Beckett, Arve Kylling, Guðmunda Sigurðardóttir, Sibylle von Löwis, and Claire Witham
Atmos. Chem. Phys., 17, 4401–4418, https://doi.org/10.5194/acp-17-4401-2017, https://doi.org/10.5194/acp-17-4401-2017, 2017
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Ash deposits can be remobilized for years following a volcanic eruption, and the resulting resuspended ash clouds can pose a significant hazard to local populations and airports. The aim of this work is to improve our ability to forecast resuspended ash storms. We use satellite imagery to constrain the emission rate of resuspended particles in an atmospheric dispersion model used to forecast resuspension events in Iceland.
Jonas Witthuhn, Hartwig Deneke, Andreas Macke, and Germar Bernhard
Atmos. Meas. Tech., 10, 709–730, https://doi.org/10.5194/amt-10-709-2017, https://doi.org/10.5194/amt-10-709-2017, 2017
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To improve and extend observational capabilities of a shipborne facility, developed within the OCEANET project for long-term investigation of the transfer of energy and material between ocean and atmosphere, a shadowband radiometer was acquired. With this instrument, automated observations of spectral irradiance components and aerosol optical properties are possible on ships. The results show that the radiometer works fine for its purposes and can compete with state of the art sun photometers.
Christos S. Zerefos, Kostas Eleftheratos, John Kapsomenakis, Stavros Solomos, Antje Inness, Dimitris Balis, Alberto Redondas, Henk Eskes, Marc Allaart, Vassilis Amiridis, Arne Dahlback, Veerle De Bock, Henri Diémoz, Ronny Engelmann, Paul Eriksen, Vitali Fioletov, Julian Gröbner, Anu Heikkilä, Irina Petropavlovskikh, Janusz Jarosławski, Weine Josefsson, Tomi Karppinen, Ulf Köhler, Charoula Meleti, Christos Repapis, John Rimmer, Vladimir Savinykh, Vadim Shirotov, Anna Maria Siani, Andrew R. D. Smedley, Martin Stanek, and René Stübi
Atmos. Chem. Phys., 17, 551–574, https://doi.org/10.5194/acp-17-551-2017, https://doi.org/10.5194/acp-17-551-2017, 2017
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The paper makes a convincing case that the Brewer network is capable of detecting enhanced SO2 columns, as observed, e.g., after volcanic eruptions. For this reason, large volcanic eruptions of the past decade have been used to detect and forecast SO2 plumes of volcanic origin using the Brewer and other ground-based networks, aided by satellite, trajectory analysis calculations and modelling.
Arve Kylling
Atmos. Meas. Tech., 9, 2103–2117, https://doi.org/10.5194/amt-9-2103-2016, https://doi.org/10.5194/amt-9-2103-2016, 2016
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During volcanic eruptions the presence of ice clouds may affect the volcanic ash signal in infrared satellite measurements. By comparison of measured infrared spectra with spectra from a radiative transfer model including both ash and ice clouds, it is shown that during the Mt Kelud February 2014 eruption, both ash and ice clouds were present simultaneously. The presence of ice clouds lowers the estimated amount of volcanic ash in the atmosphere.
Wiley Steven Bogren, John Faulkner Burkhart, and Arve Kylling
The Cryosphere, 10, 613–622, https://doi.org/10.5194/tc-10-613-2016, https://doi.org/10.5194/tc-10-613-2016, 2016
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The magnitude and makeup of error in cryospheric radiation observations due to small sensor misalignment in in situ measurements of solar irradiance is evaluated. It is shown that relatively minor sensor misalignments give significant errors in irradiance and hence albedo measurements. The total measurement error introduced by sensor tilt is dominated by the direct component. Significant measurement error can also persist in integrated daily irradiance and albedo.
G. Bernhard, A. Arola, A. Dahlback, V. Fioletov, A. Heikkilä, B. Johnsen, T. Koskela, K. Lakkala, T. Svendby, and J. Tamminen
Atmos. Chem. Phys., 15, 7391–7412, https://doi.org/10.5194/acp-15-7391-2015, https://doi.org/10.5194/acp-15-7391-2015, 2015
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Surface erythemal UV data from the Ozone Monitoring Instrument (OMI) are validated for high northern latitudes (Arctic and Scandinavia) using ground-based measurements. The bias in OMI data caused by incorrect assumptions of the surface albedo are quantified and the mechanism that causes this bias is discussed. Methods to improve the accuracy of OMI data products are presented.
A. Kylling, N. Kristiansen, A. Stohl, R. Buras-Schnell, C. Emde, and J. Gasteiger
Atmos. Meas. Tech., 8, 1935–1949, https://doi.org/10.5194/amt-8-1935-2015, https://doi.org/10.5194/amt-8-1935-2015, 2015
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Water and ice clouds affect detection and retrieval of volcanic ash clouds by satellite instruments. Synthetic infrared satellite images were generated for the Eyjafjallajokull 2010 and Grimsvotn 2011 eruptions by combining weather forecast, ash transport and radiative transfer modelling. Clouds decreased the number of pixels identified as ash and generally increased the retrieved ash-mass loading compared to the cloudless case; however, large differences were seen between scenes.
M. Karl, N. Castell, D. Simpson, S. Solberg, J. Starrfelt, T. Svendby, S.-E. Walker, and R. F. Wright
Atmos. Chem. Phys., 14, 8533–8557, https://doi.org/10.5194/acp-14-8533-2014, https://doi.org/10.5194/acp-14-8533-2014, 2014
A. Kylling, M. Kahnert, H. Lindqvist, and T. Nousiainen
Atmos. Meas. Tech., 7, 919–929, https://doi.org/10.5194/amt-7-919-2014, https://doi.org/10.5194/amt-7-919-2014, 2014
G. Bernhard, A. Dahlback, V. Fioletov, A. Heikkilä, B. Johnsen, T. Koskela, K. Lakkala, and T. Svendby
Atmos. Chem. Phys., 13, 10573–10590, https://doi.org/10.5194/acp-13-10573-2013, https://doi.org/10.5194/acp-13-10573-2013, 2013
E. Järvinen, A. Virkkula, T. Nieminen, P. P. Aalto, E. Asmi, C. Lanconelli, M. Busetto, A. Lupi, R. Schioppo, V. Vitale, M. Mazzola, T. Petäjä, V.-M. Kerminen, and M. Kulmala
Atmos. Chem. Phys., 13, 7473–7487, https://doi.org/10.5194/acp-13-7473-2013, https://doi.org/10.5194/acp-13-7473-2013, 2013
A. Kylling, R. Buras, S. Eckhardt, C. Emde, B. Mayer, and A. Stohl
Atmos. Meas. Tech., 6, 649–660, https://doi.org/10.5194/amt-6-649-2013, https://doi.org/10.5194/amt-6-649-2013, 2013
Related subject area
Subject: Gases | Research Activity: Field Measurements | Altitude Range: Stratosphere | Science Focus: Chemistry (chemical composition and reactions)
Ozone and water vapor variability in the polar middle atmosphere observed with ground-based microwave radiometers
South Pole Station ozonesondes: variability and trends in the springtime Antarctic ozone hole 1986–2021
Global seasonal distribution of CH2Br2 and CHBr3 in the upper troposphere and lower stratosphere
Redistribution of total reactive nitrogen in the lowermost Arctic stratosphere during the cold winter 2015/2016
Comparison of inorganic chlorine in the Antarctic and Arctic lowermost stratosphere by separate late winter aircraft measurements
Organic and inorganic bromine measurements around the extratropical tropopause and lowermost stratosphere: insights into the transport pathways and total bromine
Mixing at the extratropical tropopause as characterized by collocated airborne H2O and O3 lidar observations
Gravitational separation of Ar∕N2 and age of air in the lowermost stratosphere in airborne observations and a chemical transport model
Effect of deep convection on the tropical tropopause layer composition over the southwest Indian Ocean during austral summer
Investigating stratospheric changes between 2009 and 2018 with halogenated trace gas data from aircraft, AirCores, and a global model focusing on CFC-11
Bromine from short-lived source gases in the extratropical northern hemispheric upper troposphere and lower stratosphere (UTLS)
Chlorine partitioning in the lowermost Arctic vortex during the cold winter 2015/2016
Balloon-borne measurements of temperature, water vapor, ozone and aerosol backscatter on the southern slopes of the Himalayas during StratoClim 2016–2017
Mercury distribution in the upper troposphere and lowermost stratosphere according to measurements by the IAGOS-CARIBIC observatory: 2014–2016
EuBrewNet – A European Brewer network (COST Action ES1207), an overview
Stratospheric ozone measurements at Arosa (Switzerland): history and scientific relevance
Continued increase of CFC-113a (CCl3CF3) mixing ratios in the global atmosphere: emissions, occurrence and potential sources
Evaluation of stratospheric age of air from CF4, C2F6, C3F8, CHF3, HFC-125, HFC-227ea and SF6; implications for the calculations of halocarbon lifetimes, fractional release factors and ozone depletion potentials
Water vapor increase in the lower stratosphere of the Northern Hemisphere due to the Asian monsoon anticyclone observed during the TACTS/ESMVal campaigns
A refined method for calculating equivalent effective stratospheric chlorine
Hemispheric asymmetry in stratospheric NO2 trends
Mean age of stratospheric air derived from AirCore observations
Enhanced stratospheric water vapor over the summertime continental United States and the role of overshooting convection
An assessment of the climatological representativeness of IAGOS-CARIBIC trace gas measurements using EMAC model simulations
Impact of a moderate volcanic eruption on chemistry in the lower stratosphere: balloon-borne observations and model calculations
20 years of ClO measurements in the Antarctic lower stratosphere
Impact of the Asian monsoon on the extratropical lower stratosphere: trace gas observations during TACTS over Europe 2012
An objective determination of optimal site locations for detecting expected trends in upper-air temperature and total column ozone
First quasi-Lagrangian in situ measurements of Antarctic Polar springtime ozone: observed ozone loss rates from the Concordiasi long-duration balloon campaign
Constraining the N2O5 UV absorption cross section from spectroscopic trace gas measurements in the tropical mid-stratosphere
Diurnal variations of stratospheric ozone measured by ground-based microwave remote sensing at the Mauna Loa NDACC site: measurement validation and GEOSCCM model comparison
Trends in stratospheric ozone profiles using functional mixed models
Arctic stratospheric dehydration – Part 1: Unprecedented observation of vertical redistribution of water
Reconciliation of essential process parameters for an enhanced predictability of Arctic stratospheric ozone loss and its climate interactions (RECONCILE): activities and results
Re-analysis of ground-based microwave ClO measurements from Mauna Kea, 1992 to early 2012
Atmospheric test of the J(BrONO2)/kBrO+NO2 ratio: implications for total stratospheric Bry and bromine-mediated ozone loss
Stratospheric BrO abundance measured by a balloon-borne submillimeterwave radiometer
Observation-based assessment of stratospheric fractional release, lifetimes, and ozone depletion potentials of ten important source gases
Detection in the summer polar stratosphere of pollution plume from East Asia and North America by balloon-borne in situ CO measurements
Commentary on using equivalent latitude in the upper troposphere and lower stratosphere
Unusually low ozone, HCl, and HNO3 column measurements at Eureka, Canada during winter/spring 2011
ClOOCl photolysis at high solar zenith angles: analysis of the RECONCILE self-match flight
In-situ observation of Asian pollution transported into the Arctic lowermost stratosphere
Retrievals of chlorine chemistry kinetic parameters from Antarctic ClO microwave radiometer measurements
Evidence for heterogeneous chlorine activation in the tropical UTLS
A closer look at Arctic ozone loss and polar stratospheric clouds
Vertical transport rates and concentrations of OH and Cl radicals in the Tropical Tropopause Layer from observations of CO2 and halocarbons: implications for distributions of long- and short-lived chemical species
Fractional release factors of long-lived halogenated organic compounds in the tropical stratosphere
More evidence for very short-lived substance contribution to stratospheric chlorine inferred from HCl balloon-borne in situ measurements in the tropics
Guochun Shi, Witali Krochin, Eric Sauvageat, and Gunter Stober
Atmos. Chem. Phys., 23, 9137–9159, https://doi.org/10.5194/acp-23-9137-2023, https://doi.org/10.5194/acp-23-9137-2023, 2023
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We present the interannual and climatological behavior of ozone and water vapor from microwave radiometers in the Arctic.
By defining a virtual conjugate latitude station in the Southern Hemisphere, we investigate altitude-dependent interhemispheric differences and estimate the ascent and descent rates of water vapor in both hemispheres. Ozone and water vapor measurements will create a deeper understanding of the evolution of middle atmospheric ozone and water vapor.
Bryan J. Johnson, Patrick Cullis, John Booth, Irina Petropavlovskikh, Glen McConville, Birgit Hassler, Gary A. Morris, Chance Sterling, and Samuel Oltmans
Atmos. Chem. Phys., 23, 3133–3146, https://doi.org/10.5194/acp-23-3133-2023, https://doi.org/10.5194/acp-23-3133-2023, 2023
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In 1986, soon after the discovery of the Antarctic ozone hole, NOAA began year-round ozonesonde observations at South Pole Station to measure vertical profiles of ozone and temperature from the surface to 35 km. Balloon-borne ozonesondes launched at this unique site allow for tracking all phases of the yearly springtime ozone hole beginning in late winter and after sunrise, when rapid ozone depletion begins over the South Pole throughout the month of September.
Markus Jesswein, Rafael P. Fernandez, Lucas Berná, Alfonso Saiz-Lopez, Jens-Uwe Grooß, Ryan Hossaini, Eric C. Apel, Rebecca S. Hornbrook, Elliot L. Atlas, Donald R. Blake, Stephen Montzka, Timo Keber, Tanja Schuck, Thomas Wagenhäuser, and Andreas Engel
Atmos. Chem. Phys., 22, 15049–15070, https://doi.org/10.5194/acp-22-15049-2022, https://doi.org/10.5194/acp-22-15049-2022, 2022
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This study presents the global and seasonal distribution of the two major brominated short-lived substances CH2Br2 and CHBr3 in the upper troposphere and lower stratosphere based on observations from several aircraft campaigns. They show similar seasonality for both hemispheres, except in the respective hemispheric autumn lower stratosphere. A comparison with the TOMCAT and CAM-Chem models shows good agreement in the annual mean but larger differences in the seasonal consideration.
Helmut Ziereis, Peter Hoor, Jens-Uwe Grooß, Andreas Zahn, Greta Stratmann, Paul Stock, Michael Lichtenstern, Jens Krause, Vera Bense, Armin Afchine, Christian Rolf, Wolfgang Woiwode, Marleen Braun, Jörn Ungermann, Andreas Marsing, Christiane Voigt, Andreas Engel, Björn-Martin Sinnhuber, and Hermann Oelhaf
Atmos. Chem. Phys., 22, 3631–3654, https://doi.org/10.5194/acp-22-3631-2022, https://doi.org/10.5194/acp-22-3631-2022, 2022
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Airborne observations were conducted in the lowermost Arctic stratosphere during the winter of 2015/2016. The observed distribution of reactive nitrogen shows clear indications of nitrification in mid-winter and denitrification in late winter. This was caused by the formation of polar stratospheric cloud particles, which were observed during several flights. The sedimentation and evaporation of these particles and the descent of air masses cause a redistribution of reactive nitrogen.
Markus Jesswein, Heiko Bozem, Hans-Christoph Lachnitt, Peter Hoor, Thomas Wagenhäuser, Timo Keber, Tanja Schuck, and Andreas Engel
Atmos. Chem. Phys., 21, 17225–17241, https://doi.org/10.5194/acp-21-17225-2021, https://doi.org/10.5194/acp-21-17225-2021, 2021
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This study presents and compares inorganic chlorine (Cly) derived from observations with the HALO research aircraft in the Antarctic late winter–early fall 2019 and the Arctic winter 2015–2016. Trend-corrected correlations from the Northern Hemisphere show excellent agreement with those from the Southern Hemisphere. After observation allocation inside and outside the vortex based on N2O measurements, results of the two campaigns reveal substantial differences in Cly within the respective vortex.
Meike K. Rotermund, Vera Bense, Martyn P. Chipperfield, Andreas Engel, Jens-Uwe Grooß, Peter Hoor, Tilman Hüneke, Timo Keber, Flora Kluge, Benjamin Schreiner, Tanja Schuck, Bärbel Vogel, Andreas Zahn, and Klaus Pfeilsticker
Atmos. Chem. Phys., 21, 15375–15407, https://doi.org/10.5194/acp-21-15375-2021, https://doi.org/10.5194/acp-21-15375-2021, 2021
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Airborne total bromine (Brtot) and tracer measurements suggest Brtot-rich air masses persistently protruded into the lower stratosphere (LS), creating a high Brtot region over the North Atlantic in fall 2017. The main source is via isentropic transport by the Asian monsoon and to a lesser extent transport across the extratropical tropopause as quantified by a Lagrange model. The transport of Brtot via Central American hurricanes is also observed. Lastly, the impact of Brtot on LS O3 is assessed.
Andreas Schäfler, Andreas Fix, and Martin Wirth
Atmos. Chem. Phys., 21, 5217–5234, https://doi.org/10.5194/acp-21-5217-2021, https://doi.org/10.5194/acp-21-5217-2021, 2021
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First-ever, collocated ozone and water vapor lidar observations across the tropopause are applied to investigate the extratropical transition layer (ExTL). The combined view of a quasi-instantaneous cross section and its tracer–tracer depiction allows us to analyze the ExTL shape and composition and the formation of mixing lines in relation to the dynamic situation. Such lidar data are relevant for future upper-tropospheric and lower-stratospheric investigations and model validations.
Benjamin Birner, Martyn P. Chipperfield, Eric J. Morgan, Britton B. Stephens, Marianna Linz, Wuhu Feng, Chris Wilson, Jonathan D. Bent, Steven C. Wofsy, Jeffrey Severinghaus, and Ralph F. Keeling
Atmos. Chem. Phys., 20, 12391–12408, https://doi.org/10.5194/acp-20-12391-2020, https://doi.org/10.5194/acp-20-12391-2020, 2020
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With new high-precision observations from nine aircraft campaigns and 3-D chemical transport modeling, we show that the argon-to-nitrogen ratio (Ar / N2) in the lowermost stratosphere provides a useful constraint on the “age of air” (the time elapsed since entry of an air parcel into the stratosphere). Therefore, Ar / N2 in combination with traditional age-of-air indicators, such as CO2 and N2O, could provide new insights into atmospheric mixing and transport.
Stephanie Evan, Jerome Brioude, Karen Rosenlof, Sean M. Davis, Holger Vömel, Damien Héron, Françoise Posny, Jean-Marc Metzger, Valentin Duflot, Guillaume Payen, Hélène Vérèmes, Philippe Keckhut, and Jean-Pierre Cammas
Atmos. Chem. Phys., 20, 10565–10586, https://doi.org/10.5194/acp-20-10565-2020, https://doi.org/10.5194/acp-20-10565-2020, 2020
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The role of deep convection in the southwest Indian Ocean (the 3rd most active tropical cyclone basin) on the composition of the tropical tropopause layer (TTL) and the climate system is less understood due to scarce observations. Balloon-borne lidar and satellite measurements in the southwest Indian Ocean were used to study tropical cyclones' influence on TTL composition. This study compares the impact of a tropical storm and cyclone on the humidification of the TTL over the SW Indian Ocean.
Johannes C. Laube, Emma C. Leedham Elvidge, Karina E. Adcock, Bianca Baier, Carl A. M. Brenninkmeijer, Huilin Chen, Elise S. Droste, Jens-Uwe Grooß, Pauli Heikkinen, Andrew J. Hind, Rigel Kivi, Alexander Lojko, Stephen A. Montzka, David E. Oram, Steve Randall, Thomas Röckmann, William T. Sturges, Colm Sweeney, Max Thomas, Elinor Tuffnell, and Felix Ploeger
Atmos. Chem. Phys., 20, 9771–9782, https://doi.org/10.5194/acp-20-9771-2020, https://doi.org/10.5194/acp-20-9771-2020, 2020
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We demonstrate that AirCore technology, which is based on small low-cost balloons, can provide access to trace gas measurements such as CFCs at ultra-low abundances. This is a new way to quantify ozone-depleting, and related, substances in the stratosphere, which is largely inaccessible to aircraft. We show two potential uses: (a) tracking the stratospheric circulation, which is predicted to change, and (b) assessing three common meteorological reanalyses driving a global stratospheric model.
Timo Keber, Harald Bönisch, Carl Hartick, Marius Hauck, Fides Lefrancois, Florian Obersteiner, Akima Ringsdorf, Nils Schohl, Tanja Schuck, Ryan Hossaini, Phoebe Graf, Patrick Jöckel, and Andreas Engel
Atmos. Chem. Phys., 20, 4105–4132, https://doi.org/10.5194/acp-20-4105-2020, https://doi.org/10.5194/acp-20-4105-2020, 2020
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In this paper we summarize observations of short-lived halocarbons in the tropopause region. We show that, especially during winter, the levels of short-lived bromine gases at the extratropical tropopause are higher than at the tropical tropopause. We discuss the impact of the distributions on stratospheric bromine levels and compare our observations to two models with four different emission scenarios.
Andreas Marsing, Tina Jurkat-Witschas, Jens-Uwe Grooß, Stefan Kaufmann, Romy Heller, Andreas Engel, Peter Hoor, Jens Krause, and Christiane Voigt
Atmos. Chem. Phys., 19, 10757–10772, https://doi.org/10.5194/acp-19-10757-2019, https://doi.org/10.5194/acp-19-10757-2019, 2019
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We study the partitioning of inorganic chlorine into active (ozone-depleting) and reservoir species in the lowermost stratosphere of the Arctic polar vortex, using novel in situ aircraft measurements in winter 2015/2016. We observe a change in recovery pathways of the reservoirs HCl and ClONO2 with increasing potential temperature. A comparison with the CLaMS model relates the observations to the vortex-wide evolution and confirms unresolved discrepancies in the mid-winter HCl distribution.
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.
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
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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.
John S. Rimmer, Alberto Redondas, and Tomi Karppinen
Atmos. Chem. Phys., 18, 10347–10353, https://doi.org/10.5194/acp-18-10347-2018, https://doi.org/10.5194/acp-18-10347-2018, 2018
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The Vienna Convention to Protect the Ozone Layer was signed in 1985 to promote research and information exchange on the science of ozone depletion including monitoring of total ozone column and spectrally resolved solar ultraviolet radiation. This is a global challenge and, as such, all efforts to gather data should be consistent. This work has resulted in a framework for all Brewer Ozone spectrophotometers to provide data in a consistent way in terms of calibration and quality assurance.
Johannes Staehelin, Pierre Viatte, Rene Stübi, Fiona Tummon, and Thomas Peter
Atmos. Chem. Phys., 18, 6567–6584, https://doi.org/10.5194/acp-18-6567-2018, https://doi.org/10.5194/acp-18-6567-2018, 2018
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In 1926, total ozone series started in Arosa (Switzerland). Since the mid-1970s ozone is measured to document the effects of anthropogenic ozone-depleting substances (ODSs). ODSs peaked around the mid-1990s, resulting from the Montreal Protocol (1987) and its enforcement. Chemical ozone depletion stopped worsening around the mid-1990s but the large variability complicates demonstrations of the success of the protocol and the effect of ongoing climate change still requires continuous measurement.
Karina E. Adcock, Claire E. Reeves, Lauren J. Gooch, Emma C. Leedham Elvidge, Matthew J. Ashfold, Carl A. M. Brenninkmeijer, Charles Chou, Paul J. Fraser, Ray L. Langenfelds, Norfazrin Mohd Hanif, Simon O'Doherty, David E. Oram, Chang-Feng Ou-Yang, Siew Moi Phang, Azizan Abu Samah, Thomas Röckmann, William T. Sturges, and Johannes C. Laube
Atmos. Chem. Phys., 18, 4737–4751, https://doi.org/10.5194/acp-18-4737-2018, https://doi.org/10.5194/acp-18-4737-2018, 2018
Emma C. Leedham Elvidge, Harald Bönisch, Carl A. M. Brenninkmeijer, Andreas Engel, Paul J. Fraser, Eileen Gallacher, Ray Langenfelds, Jens Mühle, David E. Oram, Eric A. Ray, Anna R. Ridley, Thomas Röckmann, William T. Sturges, Ray F. Weiss, and Johannes C. Laube
Atmos. Chem. Phys., 18, 3369–3385, https://doi.org/10.5194/acp-18-3369-2018, https://doi.org/10.5194/acp-18-3369-2018, 2018
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Chemical species measured in stratospheric air can be used as proxies for stratospheric circulation changes which cannot be measured directly. A range of tracers is important to understand changing stratospheric dynamics. We demonstrate the suitability of PFCs and HFCs as tracers and support recent work that reduces the current stratospheric lifetime of SF6. Updates to policy-relevant parameters (e.g. stratospheric lifetime) linked to this change are provided for O3-depleting substances.
Christian Rolf, Bärbel Vogel, Peter Hoor, Armin Afchine, Gebhard Günther, Martina Krämer, Rolf Müller, Stefan Müller, Nicole Spelten, and Martin Riese
Atmos. Chem. Phys., 18, 2973–2983, https://doi.org/10.5194/acp-18-2973-2018, https://doi.org/10.5194/acp-18-2973-2018, 2018
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The Asian monsoon is a pronounced circulation system linked to rapid vertical transport of surface air from India and east Asia in the summer months. We found, based on aircraft measurements, higher concentration of water vapor in the lowermost stratosphere caused by the Asian monsoon. Enrichment of water vapor concentrations in the lowermost stratosphere impacts the radiation budget and thus climate. Understanding those variations in water vapor is important for climate projections.
Andreas Engel, Harald Bönisch, Jennifer Ostermöller, Martyn P. Chipperfield, Sandip Dhomse, and Patrick Jöckel
Atmos. Chem. Phys., 18, 601–619, https://doi.org/10.5194/acp-18-601-2018, https://doi.org/10.5194/acp-18-601-2018, 2018
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We present a new method to derive equivalent effective stratospheric chlorine (EESC), which is based on an improved formulation of the propagation of trends of species with chemical loss from the troposphere to the stratosphere. EESC calculated with the new method shows much better agreement with model-derived ESC. Based on this new formulation, we expect the halogen impact on midlatitude stratospheric ozone to return to 1980 values about 10 years later, then using the current formulation.
Margarita Yela, Manuel Gil-Ojeda, Mónica Navarro-Comas, David Gonzalez-Bartolomé, Olga Puentedura, Bernd Funke, Javier Iglesias, Santiago Rodríguez, Omaira García, Héctor Ochoa, and Guillermo Deferrari
Atmos. Chem. Phys., 17, 13373–13389, https://doi.org/10.5194/acp-17-13373-2017, https://doi.org/10.5194/acp-17-13373-2017, 2017
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The paper focuses on stratospheric trends of NO2, a species involved in the ozone equilibrium, using data from four NDACC stations. The global stratospheric NO2 trend has not yet been established conclusively. We analyse DOAS data from stations in the Northern Hemisphere and Southern Hemisphere during 1993–2014. The most relevant finding is the hemispheric asymmetry found in the sign of the NO2 trend, providing further evidence of changes in the stratosphere dynamics on the global scale.
Andreas Engel, Harald Bönisch, Markus Ullrich, Robert Sitals, Olivier Membrive, Francois Danis, and Cyril Crevoisier
Atmos. Chem. Phys., 17, 6825–6838, https://doi.org/10.5194/acp-17-6825-2017, https://doi.org/10.5194/acp-17-6825-2017, 2017
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AirCore is new technique for sampling stratospheric air. We present new observations of CO2 and CH4 using AirCore and derive stratospheric transport time, called the mean age of air. The purpose of using AirCore is to provide a cost-effective tool for deriving mean age. Mean age may serve as a proxy to investigate changes in stratospheric circulation. We show that there is no statistically significant trend in our 40-year time series of mean age, which is now extended using AirCore.
Robert L. Herman, Eric A. Ray, Karen H. Rosenlof, Kristopher M. Bedka, Michael J. Schwartz, William G. Read, Robert F. Troy, Keith Chin, Lance E. Christensen, Dejian Fu, Robert A. Stachnik, T. Paul Bui, and Jonathan M. Dean-Day
Atmos. Chem. Phys., 17, 6113–6124, https://doi.org/10.5194/acp-17-6113-2017, https://doi.org/10.5194/acp-17-6113-2017, 2017
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This study reports new aircraft field observations of elevated water vapor greater than 10 ppmv in the overworld stratosphere over the summertime continental US. Back trajectories from the flight track intersect overshooting convective tops within the previous 1 to 7 days, suggesting that ice is convectively and irreversibly transported to the stratosphere in the most energetic overshooting convective events. Satellite measurements (Aura MLS) indicate that such events are uncommon (< 1 %).
Johannes Eckstein, Roland Ruhnke, Andreas Zahn, Marco Neumaier, Ole Kirner, and Peter Braesicke
Atmos. Chem. Phys., 17, 2775–2794, https://doi.org/10.5194/acp-17-2775-2017, https://doi.org/10.5194/acp-17-2775-2017, 2017
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Data on atmospheric trace gases have been collected with instruments on-board a commercial airliner for more than 10 years in the CARIBIC project. We investigate which species in the dataset can be used for a representative climatology, by comparing data from the chemistry–climate model EMAC along the flight paths to a larger set of model data. We find that long-lived species are captured quite well by the CARIBIC sample while this is not the case for more variable, shorter-lived species.
Gwenaël Berthet, Fabrice Jégou, Valéry Catoire, Gisèle Krysztofiak, Jean-Baptiste Renard, Adam E. Bourassa, Doug A. Degenstein, Colette Brogniez, Marcel Dorf, Sebastian Kreycy, Klaus Pfeilsticker, Bodo Werner, Franck Lefèvre, Tjarda J. Roberts, Thibaut Lurton, Damien Vignelles, Nelson Bègue, Quentin Bourgeois, Daniel Daugeron, Michel Chartier, Claude Robert, Bertrand Gaubicher, and Christophe Guimbaud
Atmos. Chem. Phys., 17, 2229–2253, https://doi.org/10.5194/acp-17-2229-2017, https://doi.org/10.5194/acp-17-2229-2017, 2017
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Since the last major volcanic event, i.e. the Pinatubo eruption in 1991, only
moderateeruptions have regularly injected sulfur into the stratosphere, typically enhancing the aerosol loading for several months. We investigate here for the first time the chemical perturbation associated with the Sarychev eruption in June 2009, using balloon-borne instruments and model calculations. Some chemical compounds are significantly affected by the aerosols, but the impact on stratospheric ozone is weak.
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.
Stefan Müller, Peter Hoor, Heiko Bozem, Ellen Gute, Bärbel Vogel, Andreas Zahn, Harald Bönisch, Timo Keber, Martina Krämer, Christian Rolf, Martin Riese, Hans Schlager, and Andreas Engel
Atmos. Chem. Phys., 16, 10573–10589, https://doi.org/10.5194/acp-16-10573-2016, https://doi.org/10.5194/acp-16-10573-2016, 2016
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In situ airborne measurements performed during TACTS/ESMVal 2012 were analysed to investigate the chemical compostion of the upper troposphere and lower stratosphere. N2O, CO and O3 data show an increase in tropospherically affected air masses within the extratropical stratosphere from August to September 2012, which originate from the Asian monsoon region. Thus, the Asian monsoon anticyclone significantly affected the chemical composition of the extratropical stratosphere during summer 2012.
K. Kreher, G. E. Bodeker, and M. Sigmond
Atmos. Chem. Phys., 15, 7653–7665, https://doi.org/10.5194/acp-15-7653-2015, https://doi.org/10.5194/acp-15-7653-2015, 2015
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This manuscript aims to answer the following question: which of the existing sites engaged in upper-air temperature measurements are best located to detect expected future trends within the shortest time possible? To do so, we explore one objective method for selecting the optimal locations for detecting projected 21st century trends and then demonstrate a similar technique for objectively selecting optimal locations for detecting expected future trends in total column ozone.
R. Schofield, L. M. Avallone, L. E. Kalnajs, A. Hertzog, I. Wohltmann, and M. Rex
Atmos. Chem. Phys., 15, 2463–2472, https://doi.org/10.5194/acp-15-2463-2015, https://doi.org/10.5194/acp-15-2463-2015, 2015
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Ozone measurements onboard three Concordiasi balloons flown in the stratosphere in
the Antarctic spring of 2010 are presented. These measurements are the first long-duration in situ measurements of Antarctic springtime stratospheric ozone. By matching air parcels, ozone loss rates where derived. Downwind of the Antarctic Peninsula, very large ozone losses of up to 230 ppb per day or 16 ppbv per sunlit hour were observed. These high rates are consistent with almost complete chlorine activation.
L. Kritten, A. Butz, M. P. Chipperfield, M. Dorf, S. Dhomse, R. Hossaini, H. Oelhaf, C. Prados-Roman, G. Wetzel, and K. Pfeilsticker
Atmos. Chem. Phys., 14, 9555–9566, https://doi.org/10.5194/acp-14-9555-2014, https://doi.org/10.5194/acp-14-9555-2014, 2014
A. Parrish, I. S. Boyd, G. E. Nedoluha, P. K. Bhartia, S. M. Frith, N. A. Kramarova, B. J. Connor, G. E. Bodeker, L. Froidevaux, M. Shiotani, and T. Sakazaki
Atmos. Chem. Phys., 14, 7255–7272, https://doi.org/10.5194/acp-14-7255-2014, https://doi.org/10.5194/acp-14-7255-2014, 2014
A. Park, S. Guillas, and I. Petropavlovskikh
Atmos. Chem. Phys., 13, 11473–11501, https://doi.org/10.5194/acp-13-11473-2013, https://doi.org/10.5194/acp-13-11473-2013, 2013
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
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
B. J. Connor, T. Mooney, G. E. Nedoluha, J. W. Barrett, A. Parrish, J. Koda, M. L. Santee, and R. M. Gomez
Atmos. Chem. Phys., 13, 8643–8650, https://doi.org/10.5194/acp-13-8643-2013, https://doi.org/10.5194/acp-13-8643-2013, 2013
S. Kreycy, C. Camy-Peyret, M. P. Chipperfield, M. Dorf, W. Feng, R. Hossaini, L. Kritten, B. Werner, and K. Pfeilsticker
Atmos. Chem. Phys., 13, 6263–6274, https://doi.org/10.5194/acp-13-6263-2013, https://doi.org/10.5194/acp-13-6263-2013, 2013
R. A. Stachnik, L. Millán, R. Jarnot, R. Monroe, C. McLinden, S. Kühl, J. Puķīte, M. Shiotani, M. Suzuki, Y. Kasai, F. Goutail, J. P. Pommereau, M. Dorf, and K. Pfeilsticker
Atmos. Chem. Phys., 13, 3307–3319, https://doi.org/10.5194/acp-13-3307-2013, https://doi.org/10.5194/acp-13-3307-2013, 2013
J. C. Laube, A. Keil, H. Bönisch, A. Engel, T. Röckmann, C. M. Volk, and W. T. Sturges
Atmos. Chem. Phys., 13, 2779–2791, https://doi.org/10.5194/acp-13-2779-2013, https://doi.org/10.5194/acp-13-2779-2013, 2013
G. Krysztofiak, R. Thiéblemont, N. Huret, V. Catoire, Y. Té, F. Jégou, P. F. Coheur, C. Clerbaux, S. Payan, M. A. Drouin, C. Robert, P. Jeseck, J.-L. Attié, and C. Camy-Peyret
Atmos. Chem. Phys., 12, 11889–11906, https://doi.org/10.5194/acp-12-11889-2012, https://doi.org/10.5194/acp-12-11889-2012, 2012
L. L. Pan, A. Kunz, C. R. Homeyer, L. A. Munchak, D. E. Kinnison, and S. Tilmes
Atmos. Chem. Phys., 12, 9187–9199, https://doi.org/10.5194/acp-12-9187-2012, https://doi.org/10.5194/acp-12-9187-2012, 2012
R. Lindenmaier, K. Strong, R. L. Batchelor, M. P. Chipperfield, W. H. Daffer, J. R. Drummond, T. J. Duck, H. Fast, W. Feng, P. F. Fogal, F. Kolonjari, G. L. Manney, A. Manson, C. Meek, R. L. Mittermeier, G. J. Nott, C. Perro, and K. A. Walker
Atmos. Chem. Phys., 12, 3821–3835, https://doi.org/10.5194/acp-12-3821-2012, https://doi.org/10.5194/acp-12-3821-2012, 2012
O. Sumińska-Ebersoldt, R. Lehmann, T. Wegner, J.-U. Grooß, E. Hösen, R. Weigel, W. Frey, S. Griessbach, V. Mitev, C. Emde, C. M. Volk, S. Borrmann, M. Rex, F. Stroh, and M. von Hobe
Atmos. Chem. Phys., 12, 1353–1365, https://doi.org/10.5194/acp-12-1353-2012, https://doi.org/10.5194/acp-12-1353-2012, 2012
A. Roiger, H. Schlager, A. Schäfler, H. Huntrieser, M. Scheibe, H. Aufmhoff, O. R. Cooper, H. Sodemann, A. Stohl, J. Burkhart, M. Lazzara, C. Schiller, K. S. Law, and F. Arnold
Atmos. Chem. Phys., 11, 10975–10994, https://doi.org/10.5194/acp-11-10975-2011, https://doi.org/10.5194/acp-11-10975-2011, 2011
S. Kremser, R. Schofield, G. E. Bodeker, B. J. Connor, M. Rex, J. Barret, T. Mooney, R. J. Salawitch, T. Canty, K. Frieler, M. P. Chipperfield, U. Langematz, and W. Feng
Atmos. Chem. Phys., 11, 5183–5193, https://doi.org/10.5194/acp-11-5183-2011, https://doi.org/10.5194/acp-11-5183-2011, 2011
M. von Hobe, J.-U. Grooß, G. Günther, P. Konopka, I. Gensch, M. Krämer, N. Spelten, A. Afchine, C. Schiller, A. Ulanovsky, N. Sitnikov, G. Shur, V. Yushkov, F. Ravegnani, F. Cairo, A. Roiger, C. Voigt, H. Schlager, R. Weigel, W. Frey, S. Borrmann, R. Müller, and F. Stroh
Atmos. Chem. Phys., 11, 241–256, https://doi.org/10.5194/acp-11-241-2011, https://doi.org/10.5194/acp-11-241-2011, 2011
N. R. P. Harris, R. Lehmann, M. Rex, and P. von der Gathen
Atmos. Chem. Phys., 10, 8499–8510, https://doi.org/10.5194/acp-10-8499-2010, https://doi.org/10.5194/acp-10-8499-2010, 2010
S. Park, E. L. Atlas, R. Jiménez, B. C. Daube, E. W. Gottlieb, J. Nan, D. B. A. Jones, L. Pfister, T. J. Conway, T. P. Bui, R.-S. Gao, and S. C. Wofsy
Atmos. Chem. Phys., 10, 6669–6684, https://doi.org/10.5194/acp-10-6669-2010, https://doi.org/10.5194/acp-10-6669-2010, 2010
J. C. Laube, A. Engel, H. Bönisch, T. Möbius, W. T. Sturges, M. Braß, and T. Röckmann
Atmos. Chem. Phys., 10, 1093–1103, https://doi.org/10.5194/acp-10-1093-2010, https://doi.org/10.5194/acp-10-1093-2010, 2010
Y. Mébarki, V. Catoire, N. Huret, G. Berthet, C. Robert, and G. Poulet
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Short summary
Measurements of total ozone and effective cloud transmittance (eCLT) have been performed since 1995 at three Norwegian sites with GUV multi-filter instruments. The unique data sets of high-time-resolution measurements can be used for a broad range of studies. Data analyses reveal an increase in total ozone above Norway from 1995 to 2019. Measurements of GUV eCLT indicate changes in albedo in Ny-Ålesund (Svalbard) during the past 25 years, most likely resulting from increased Arctic ice melt.
Measurements of total ozone and effective cloud transmittance (eCLT) have been performed since...
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