Articles | Volume 19, issue 5
https://doi.org/10.5194/acp-19-3257-2019
© Author(s) 2019. 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-19-3257-2019
© Author(s) 2019. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Research article
| Highlight paper
| 
13 Mar 2019
Research article | Highlight paper |
| 13 Mar 2019
| 13 Mar 2019
Trends in global tropospheric ozone inferred from a composite record of TOMS/OMI/MLS/OMPS satellite measurements and the MERRA-2 GMI simulation
Jerry R. Ziemke
CORRESPONDING AUTHOR
NASA Goddard Space Flight Center, Greenbelt, Maryland, USA
Morgan State University, Baltimore, Maryland, USA
Luke D. Oman
NASA Goddard Space Flight Center, Greenbelt, Maryland, USA
Sarah A. Strode
NASA Goddard Space Flight Center, Greenbelt, Maryland, USA
Universities Space Research Association, Columbia, Maryland, USA
Anne R. Douglass
NASA Goddard Space Flight Center, Greenbelt, Maryland, USA
Mark A. Olsen
NASA Goddard Space Flight Center, Greenbelt, Maryland, USA
Morgan State University, Baltimore, Maryland, USA
Richard D. McPeters
NASA Goddard Space Flight Center, Greenbelt, Maryland, USA
Pawan K. Bhartia
NASA Goddard Space Flight Center, Greenbelt, Maryland, USA
Lucien Froidevaux
NASA Jet Propulsion Laboratory, Pasadena, California, USA
Gordon J. Labow
Science Systems and Applications, Inc. (SSAI), Lanham, Maryland, USA
Jacquie C. Witte
Science Systems and Applications, Inc. (SSAI), Lanham, Maryland, USA
Anne M. Thompson
NASA Goddard Space Flight Center, Greenbelt, Maryland, USA
David P. Haffner
Science Systems and Applications, Inc. (SSAI), Lanham, Maryland, USA
Natalya A. Kramarova
NASA Goddard Space Flight Center, Greenbelt, Maryland, USA
Stacey M. Frith
Science Systems and Applications, Inc. (SSAI), Lanham, Maryland, USA
Liang-Kang Huang
Science Systems and Applications, Inc. (SSAI), Lanham, Maryland, USA
Glen R. Jaross
NASA Goddard Space Flight Center, Greenbelt, Maryland, USA
Colin J. Seftor
Science Systems and Applications, Inc. (SSAI), Lanham, Maryland, USA
Mathew T. Deland
Science Systems and Applications, Inc. (SSAI), Lanham, Maryland, USA
Steven L. Taylor
Science Systems and Applications, Inc. (SSAI), Lanham, Maryland, USA
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Zhou Zang, Jane Liu, David Tarasick, Omid Moeini, Jianchun Bian, Jinqiang Zhang, Anne M. Thompson, Roeland Van Malderen, Herman G. J. Smit, Ryan M. Stauffer, Bryan J. Johnson, and Debra E. Kollonige
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Andrea Orfanoz-Cheuquelaf, Carlo Arosio, Alexei Rozanov, Mark Weber, Annette Ladstätter-Weißenmayer, John P. Burrows, Anne M. Thompson, Ryan M. Stauffer, and Debra E. Kollonige
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Yasin Elshorbany, Jerald Ziemke, Sarah Strode, Hervé Petetin, Kazuyuki Miyazaki, Isabelle De Smedt, Kenneth Pickering, Rodrigo Seguel, Helen Worden, Tamara Emmerichs, Domenico Taraborrelli, Maria Cazorla, Suvarna Fadnavis, Rebecca Buchholz, Benjamin Gaubert, Néstor Rojas, Thiago Nogueira, Thérèse Salameh, and Min Huang
EGUsphere, https://doi.org/10.5194/egusphere-2024-720, https://doi.org/10.5194/egusphere-2024-720, 2024
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We investigated tropospheric ozone spatial variability and trends from 2005 to 2019 and related those to ozone precursors on global and regional scales. We also investigate the spatiotemporal characteristics of the ozone formation regime in relation to ozone chemical sources and sinks. Our analysis is based on remote sensing products of the Tropospheric Column of Ozone and its precursors, nitrogen dioxide, formaldehyde, and total column of CO as well as ozonesonde data and model simulations.
Lucien Froidevaux, Douglas E. Kinnison, Benjamin Gaubert, Michael J. Schwartz, Nathaniel J. Livesey, William G. Read, Charles G. Bardeen, Jerry R. Ziemke, and Ryan A. Fuller
EGUsphere, https://doi.org/10.5194/egusphere-2024-525, https://doi.org/10.5194/egusphere-2024-525, 2024
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We compare observed changes in ozone (O3) and carbon monoxide (CO) in the tropical upper troposphere (10–15 km altitude) for 2005–2020 to predictions from model simulations that track the evolution of natural and industrial emissions transported to this region. An increasing trend in measured upper tropospheric O3 is generally well matched by the model trends. We also find that changes in modeled industrial CO surface emissions lead to better model agreement with observed decreasing CO trends.
Adriana Rocha-Lima, Peter R. Colarco, Anton S. Darmenov, Edward P. Nowottnick, Arlindo M. da Silva, and Luke D. Oman
Atmos. Chem. Phys., 24, 2443–2464, https://doi.org/10.5194/acp-24-2443-2024, https://doi.org/10.5194/acp-24-2443-2024, 2024
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Observations show an increasing aerosol optical depth trend in the Middle East between 2003–2012. We evaluate the NASA Goddard Earth Observing System (GEOS) model's ability to capture these trends and examine the meteorological and surface parameters driving dust emissions. Our results highlight the importance of data assimilation for long-term trends of atmospheric aerosols and support the hypothesis that vegetation cover loss may have contributed to increasing dust emissions in the period.
Swathi Maratt Satheesan, Kai-Uwe Eichmann, John P. Burrows, Mark Weber, Ryan Stauffer, Anne M. Thompson, and Debra Kollonige
EGUsphere, https://doi.org/10.5194/egusphere-2023-2825, https://doi.org/10.5194/egusphere-2023-2825, 2024
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CHORA, an advanced CCD technique, enhances the accuracy of tropospheric ozone retrievals. Unlike the traditional Pacific cloud reference sector (CPC) scheme, CHORA introduces a local cloud reference sector (CLC ) and an alternative approach (CLCT) for precision. Analysing monthly averaged TROPOMI data from 2018 to 2022 and validating with SHADOZ ozonesonde data, CLCT outperforms other methods, emerging as the preferred choice, especially in future geostationary satellite missions.
Min Huang, Gregory R. Carmichael, James H. Crawford, Kevin W. Bowman, Isabelle De Smedt, Andreas Colliander, Michael H. Cosh, Sujay V. Kumar, Alex B. Guenther, Scott J. Janz, Ryan M. Stauffer, Anne M. Thompson, Niko M. Fedkin, Robert J. Swap, John D. Bolten, and Alicia T. Joseph
EGUsphere, https://doi.org/10.5194/egusphere-2024-484, https://doi.org/10.5194/egusphere-2024-484, 2024
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This study uses model simulations along with multiplatform, multidisciplinary observations and a range of analysis methods to estimate and understand the distributions, temporal changes, and impacts of reactive nitrogen and ozone over the most populous US region that has undergone significant environmental changes. Deposition, biogenic emissions, and extra-regional sources have been playing increasingly important roles in controlling pollutants’ budgets in this area as local emissions go down.
Herman G. J. Smit, Deniz Poyraz, Roeland Van Malderen, Anne M. Thompson, David W. Tarasick, Ryan M. Stauffer, Bryan J. Johnson, and Debra E. Kollonige
Atmos. Meas. Tech., 17, 73–112, https://doi.org/10.5194/amt-17-73-2024, https://doi.org/10.5194/amt-17-73-2024, 2024
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This paper revisits fundamentals of ECC ozonesonde measurements to develop and characterize a methodology to correct for the fast and slow time responses using the JOSIE (Jülich Ozone Sonde Intercomparison Experiment) simulation chamber data. Comparing the new corrected ozonesonde profiles to an accurate ozone UV photometer (OPM) as reference allows us to evaluate the time response correction (TRC) method and to determine calibration functions traceable to one reference with 5 % uncertainty.
Jay Herman, Jerald Ziemke, and Richard McPeters
Atmos. Meas. Tech., 16, 4693–4707, https://doi.org/10.5194/amt-16-4693-2023, https://doi.org/10.5194/amt-16-4693-2023, 2023
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Fourier series multivariate linear regression trends (% per decade) in ozone were estimated from the Merged Ozone Data Set (MOD) from 1979 to 2021 in two different regimes, from 1979 to TA (the date when ozone stopped decreasing) and TA to 2021. The derived TA is a latitude-dependent date, ranging from 1994 to 1998. TA(θ) is a marker for photochemistry dynamics models attempting to represent ozone change over the past 42 years.
Daniel C. Anderson, Bryan N. Duncan, Julie M. Nicely, Junhua Liu, Sarah A. Strode, and Melanie B. Follette-Cook
Atmos. Chem. Phys., 23, 6319–6338, https://doi.org/10.5194/acp-23-6319-2023, https://doi.org/10.5194/acp-23-6319-2023, 2023
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We describe a methodology that combines machine learning, satellite observations, and 3D chemical model output to infer the abundance of the hydroxyl radical (OH), a chemical that removes many trace gases from the atmosphere. The methodology successfully captures the variability of observed OH, although further observations are needed to evaluate absolute accuracy. Current satellite observations are of sufficient quality to infer OH, but retrieval validation in the remote tropics is needed.
Viral Shah, Daniel J. Jacob, Ruijun Dang, Lok N. Lamsal, Sarah A. Strode, Stephen D. Steenrod, K. Folkert Boersma, Sebastian D. Eastham, Thibaud M. Fritz, Chelsea Thompson, Jeff Peischl, Ilann Bourgeois, Ilana B. Pollack, Benjamin A. Nault, Ronald C. Cohen, Pedro Campuzano-Jost, Jose L. Jimenez, Simone T. Andersen, Lucy J. Carpenter, Tomás Sherwen, and Mat J. Evans
Atmos. Chem. Phys., 23, 1227–1257, https://doi.org/10.5194/acp-23-1227-2023, https://doi.org/10.5194/acp-23-1227-2023, 2023
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NOx in the free troposphere (above 2 km) affects global tropospheric chemistry and the retrieval and interpretation of satellite NO2 measurements. We evaluate free tropospheric NOx in global atmospheric chemistry models and find that recycling NOx from its reservoirs over the oceans is faster than that simulated in the models, resulting in increases in simulated tropospheric ozone and OH. Over the U.S., free tropospheric NO2 contributes the majority of the tropospheric NO2 column in summer.
Hao Guo, Clare M. Flynn, Michael J. Prather, Sarah A. Strode, Stephen D. Steenrod, Louisa Emmons, Forrest Lacey, Jean-Francois Lamarque, Arlene M. Fiore, Gus Correa, Lee T. Murray, Glenn M. Wolfe, Jason M. St. Clair, Michelle Kim, John Crounse, Glenn Diskin, Joshua DiGangi, Bruce C. Daube, Roisin Commane, Kathryn McKain, Jeff Peischl, Thomas B. Ryerson, Chelsea Thompson, Thomas F. Hanisco, Donald Blake, Nicola J. Blake, Eric C. Apel, Rebecca S. Hornbrook, James W. Elkins, Eric J. Hintsa, Fred L. Moore, and Steven C. Wofsy
Atmos. Chem. Phys., 23, 99–117, https://doi.org/10.5194/acp-23-99-2023, https://doi.org/10.5194/acp-23-99-2023, 2023
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We have prepared a unique and unusual result from the recent ATom aircraft mission: a measurement-based derivation of the production and loss rates of ozone and methane over the ocean basins. These are the key products of chemistry models used in assessments but have thus far lacked observational metrics. It also shows the scales of variability of atmospheric chemical rates and provides a major challenge to the atmospheric models.
Amy Christiansen, Loretta J. Mickley, Junhua Liu, Luke D. Oman, and Lu Hu
Atmos. Chem. Phys., 22, 14751–14782, https://doi.org/10.5194/acp-22-14751-2022, https://doi.org/10.5194/acp-22-14751-2022, 2022
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Understanding tropospheric ozone trends is crucial for accurate predictions of future air quality and climate, but drivers of trends are not well understood. We analyze global tropospheric ozone trends since 1980 using ozonesonde and surface measurements, and we evaluate two models for their ability to reproduce trends. We find observational evidence of increasing tropospheric ozone, but models underestimate these increases. This hinders our ability to estimate ozone radiative forcing.
Sarah A. Strode, Ghassan Taha, Luke D. Oman, Robert Damadeo, David Flittner, Mark Schoeberl, Christopher E. Sioris, and Ryan Stauffer
Atmos. Meas. Tech., 15, 6145–6161, https://doi.org/10.5194/amt-15-6145-2022, https://doi.org/10.5194/amt-15-6145-2022, 2022
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We use a global atmospheric chemistry model simulation to generate scaling factors that account for the daily cycle of NO2 and ozone. These factors facilitate comparisons between sunrise and sunset observations from SAGE III/ISS and observations from other instruments. We provide the scaling factors as monthly zonal means for different latitudes and altitudes. We find that applying these factors yields more consistent comparisons between observations from SAGE III/ISS and other instruments.
Klaus-Peter Heue, Diego Loyola, Fabian Romahn, Walter Zimmer, Simon Chabrillat, Quentin Errera, Jerry Ziemke, and Natalya Kramarova
Atmos. Meas. Tech., 15, 5563–5579, https://doi.org/10.5194/amt-15-5563-2022, https://doi.org/10.5194/amt-15-5563-2022, 2022
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To retrieve tropospheric ozone column information, we subtract stratospheric column data of BASCOE from TROPOMI/S5P total ozone columns.
The new S5P-BASCOE data agree well with existing tropospheric data like OMPS-MERRA-2. The data are also compared to ozone soundings.
The tropospheric ozone columns show the expected temporal and spatial patterns. We will also apply the algorithm to future UV nadir missions like Sentinel 4 or 5 or to recent and ongoing missions like GOME_2 or OMI.
Sophie Godin-Beekmann, Niramson Azouz, Viktoria F. Sofieva, Daan Hubert, Irina Petropavlovskikh, Peter Effertz, Gérard Ancellet, Doug A. Degenstein, Daniel Zawada, Lucien Froidevaux, Stacey Frith, Jeannette Wild, Sean Davis, Wolfgang Steinbrecht, Thierry Leblanc, Richard Querel, Kleareti Tourpali, Robert Damadeo, Eliane Maillard Barras, René Stübi, Corinne Vigouroux, Carlo Arosio, Gerald Nedoluha, Ian Boyd, Roeland Van Malderen, Emmanuel Mahieu, Dan Smale, and Ralf Sussmann
Atmos. Chem. Phys., 22, 11657–11673, https://doi.org/10.5194/acp-22-11657-2022, https://doi.org/10.5194/acp-22-11657-2022, 2022
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An updated evaluation up to 2020 of stratospheric ozone profile long-term trends at extrapolar latitudes based on satellite and ground-based records is presented. Ozone increase in the upper stratosphere is confirmed, with significant trends at most latitudes. In this altitude region, a very good agreement is found with trends derived from chemistry–climate model simulations. Observed and modelled trends diverge in the lower stratosphere, but the differences are non-significant.
John T. Sullivan, Arnoud Apituley, Nora Mettig, Karin Kreher, K. Emma Knowland, Marc Allaart, Ankie Piters, Michel Van Roozendael, Pepijn Veefkind, Jerry R. Ziemke, Natalya Kramarova, Mark Weber, Alexei Rozanov, Laurence Twigg, Grant Sumnicht, and Thomas J. McGee
Atmos. Chem. Phys., 22, 11137–11153, https://doi.org/10.5194/acp-22-11137-2022, https://doi.org/10.5194/acp-22-11137-2022, 2022
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A TROPOspheric Monitoring Instrument (TROPOMI) validation campaign (TROLIX-19) was held in the Netherlands in September 2019. The research presented here focuses on using ozone lidars from NASA’s Goddard Space Flight Center to better evaluate the characterization of ozone throughout TROLIX-19 as compared to balloon-borne, space-borne and ground-based passive measurements, as well as a global coupled chemistry meteorology model.
Daniel C. Anderson, Melanie B. Follette-Cook, Sarah A. Strode, Julie M. Nicely, Junhua Liu, Peter D. Ivatt, and Bryan N. Duncan
Geosci. Model Dev., 15, 6341–6358, https://doi.org/10.5194/gmd-15-6341-2022, https://doi.org/10.5194/gmd-15-6341-2022, 2022
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The hydroxyl radical (OH) is the most important chemical in the atmosphere for removing certain pollutants, including methane, the second-most-important greenhouse gas. We present a methodology to create an easily modifiable parameterization that can calculate OH concentrations in a computationally efficient way. The parameterization, which predicts OH within 5 %, can be integrated into larger climate models to allow for calculation of the interactions between OH, methane, and other chemicals.
Jay Herman, Liang Huang, David Hafner, and Adam Szabo
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2022-481, https://doi.org/10.5194/acp-2022-481, 2022
Publication in ACP not foreseen
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The research object is to see if reflections from clouds by the DSCOVR satellite at the Earth-Sun Lagrange point are enhanced as the backscattering angle nears 180 degrees. The 388 nm wavelength channel sees almost nothing from the Earth's surface. The result is that the Southern Hemisphere radiance increase in December 2020 and 2021 is likely caused by cloud amount increase and not by enhanced reflectivity at a 178-degree backscatter angle.
Quintus Kleipool, Nico Rozemeijer, Mirna van Hoek, Jonatan Leloux, Erwin Loots, Antje Ludewig, Emiel van der Plas, Daley Adrichem, Raoul Harel, Simon Spronk, Mark ter Linden, Glen Jaross, David Haffner, Pepijn Veefkind, and Pieternel F. Levelt
Atmos. Meas. Tech., 15, 3527–3553, https://doi.org/10.5194/amt-15-3527-2022, https://doi.org/10.5194/amt-15-3527-2022, 2022
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A new collection-4 dataset for the Ozone Monitoring Instrument (OMI) mission has been established to supersede the current collection-3 level-1b (L1b) data, produced with a newly developed L01b data processor based on the TROPOspheric Monitoring Instrument (TROPOMI) L01b processor. The collection-4 L1b data have a similar output format to the TROPOMI L1b data for easy connection of the data series. Many insights from the TROPOMI algorithms, as well as from OMI collection-3 usage, were included.
Mark Weber, Carlo Arosio, Melanie Coldewey-Egbers, Vitali E. Fioletov, Stacey M. Frith, Jeannette D. Wild, Kleareti Tourpali, John P. Burrows, and Diego Loyola
Atmos. Chem. Phys., 22, 6843–6859, https://doi.org/10.5194/acp-22-6843-2022, https://doi.org/10.5194/acp-22-6843-2022, 2022
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Long-term trends in column ozone have been determined from five merged total ozone datasets spanning the period 1978–2020. We show that ozone recovery due to the decline in stratospheric halogens after the 1990s (as regulated by the Montreal Protocol) is evident outside the tropical region and amounts to half a percent per decade. The ozone recovery in the Northern Hemisphere is however compensated for by the negative long-term trend contribution from atmospheric dynamics since the year 2000.
Nora Mettig, Mark Weber, Alexei Rozanov, John P. Burrows, Pepijn Veefkind, Anne M. Thompson, Ryan M. Stauffer, Thierry Leblanc, Gerard Ancellet, Michael J. Newchurch, Shi Kuang, Rigel Kivi, Matthew B. Tully, Roeland Van Malderen, Ankie Piters, Bogumil Kois, René Stübi, and Pavla Skrivankova
Atmos. Meas. Tech., 15, 2955–2978, https://doi.org/10.5194/amt-15-2955-2022, https://doi.org/10.5194/amt-15-2955-2022, 2022
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Vertical ozone profiles from combined spectral measurements in the UV and IR spectral ranges were retrieved by using data from TROPOMI/S5P and CrIS/Suomi-NPP. The vertical resolution and accuracy of the ozone profiles are improved by combining both wavelength ranges compared to retrievals limited to UV or IR spectral data only. The advancement of our TOPAS algorithm for combined measurements is required because in the UV-only retrieval the vertical resolution in the troposphere is very limited.
Nikos Daskalakis, Laura Gallardo, Maria Kanakidou, Johann Rasmus Nüß, Camilo Menares, Roberto Rondanelli, Anne M. Thompson, and Mihalis Vrekoussis
Atmos. Chem. Phys., 22, 4075–4099, https://doi.org/10.5194/acp-22-4075-2022, https://doi.org/10.5194/acp-22-4075-2022, 2022
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Forest fires emit carbon monoxide (CO) that can be transported into the atmosphere far from the sources and reacts to produce ozone (O3) that affects climate, ecosystems and health. O3 is also produced in the stratosphere and can be transported downwards. Using a global numerical model, we found that forest fires can affect CO and O3 even in the South Pacific, the most pristine region of the global ocean, but transport from the stratosphere is a more important O3 source than fires in the region.
Patrick E. Sheese, Kaley A. Walker, Chris D. Boone, Adam E. Bourassa, Doug A. Degenstein, Lucien Froidevaux, C. Thomas McElroy, Donal Murtagh, James M. Russell III, and Jiansheng Zou
Atmos. Meas. Tech., 15, 1233–1249, https://doi.org/10.5194/amt-15-1233-2022, https://doi.org/10.5194/amt-15-1233-2022, 2022
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This study analyzes the quality of two versions (v3.6 and v4.1) of ozone concentration measurements from the ACE-FTS (Atmospheric Chemistry Experiment Fourier Transform Spectrometer), by comparing with data from five satellite instruments between 2004 and 2020. It was found that although the v3.6 data exhibit a better agreement than v4.1 with respect to the other instruments, v4.1 exhibits much better stability over time than v3.6. The stability of v4.1 makes it suitable for ozone trend studies.
Nick Gorkavyi, Nickolay Krotkov, Can Li, Leslie Lait, Peter Colarco, Simon Carn, Matthew DeLand, Paul Newman, Mark Schoeberl, Ghassan Taha, Omar Torres, Alexander Vasilkov, and Joanna Joiner
Atmos. Meas. Tech., 14, 7545–7563, https://doi.org/10.5194/amt-14-7545-2021, https://doi.org/10.5194/amt-14-7545-2021, 2021
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The 21 June 2019 eruption of the Raikoke volcano produced significant amounts of volcanic aerosols (sulfate and ash) and sulfur dioxide (SO2) gas that penetrated into the lower stratosphere. We showed that the amount of SO2 decreases with a characteristic period of 8–18 d and the peak of sulfate aerosol lags the initial peak of SO2 by 1.5 months. We also examined the dynamics of an unusual stratospheric coherent circular cloud of SO2 and aerosol observed from 18 July to 22 September 2019.
Daan Hubert, Klaus-Peter Heue, Jean-Christopher Lambert, Tijl Verhoelst, Marc Allaart, Steven Compernolle, Patrick D. Cullis, Angelika Dehn, Christian Félix, Bryan J. Johnson, Arno Keppens, Debra E. Kollonige, Christophe Lerot, Diego Loyola, Matakite Maata, Sukarni Mitro, Maznorizan Mohamad, Ankie Piters, Fabian Romahn, Henry B. Selkirk, Francisco R. da Silva, Ryan M. Stauffer, Anne M. Thompson, J. Pepijn Veefkind, Holger Vömel, Jacquelyn C. Witte, and Claus Zehner
Atmos. Meas. Tech., 14, 7405–7433, https://doi.org/10.5194/amt-14-7405-2021, https://doi.org/10.5194/amt-14-7405-2021, 2021
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We assess the first 2 years of TROPOMI tropical tropospheric ozone column data. Comparisons to reference measurements by ozonesonde and satellite sensors show that TROPOMI bias (−0.1 to +2.3 DU) and precision (1.5 to 2.5 DU) meet mission requirements. Potential causes of bias and its spatio-temporal structure are discussed, as well as ways to identify sampling errors. Our analysis of known geophysical patterns demonstrates the improved performance of TROPOMI with respect to its predecessors.
Gaëlle Dufour, Didier Hauglustaine, Yunjiang Zhang, Maxim Eremenko, Yann Cohen, Audrey Gaudel, Guillaume Siour, Mathieu Lachatre, Axel Bense, Bertrand Bessagnet, Juan Cuesta, Jerry Ziemke, Valérie Thouret, and Bo Zheng
Atmos. Chem. Phys., 21, 16001–16025, https://doi.org/10.5194/acp-21-16001-2021, https://doi.org/10.5194/acp-21-16001-2021, 2021
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The IASI observations and the LMDZ-OR-INCA model simulations show negative ozone trends in the Central East China region in the lower free (3–6 km column) and the upper free (6–9 km column) troposphere. Sensitivity studies from the model show that the Chinese anthropogenic emissions contribute to more than 50 % in the trend. The reduction in NOx emissions that has occurred since 2013 in China seems to lead to a decrease in ozone in the free troposphere, contrary to the increase at the surface.
Nathaniel J. Livesey, William G. Read, Lucien Froidevaux, Alyn Lambert, Michelle L. Santee, Michael J. Schwartz, Luis F. Millán, Robert F. Jarnot, Paul A. Wagner, Dale F. Hurst, Kaley A. Walker, Patrick E. Sheese, and Gerald E. Nedoluha
Atmos. Chem. Phys., 21, 15409–15430, https://doi.org/10.5194/acp-21-15409-2021, https://doi.org/10.5194/acp-21-15409-2021, 2021
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The Microwave Limb Sounder (MLS), an instrument on NASA's Aura mission launched in 2004, measures vertical profiles of the temperature and composition of Earth's "middle atmosphere" (the region from ~12 to ~100 km altitude). We describe how, among the 16 trace gases measured by MLS, the measurements of water vapor (H2O) and nitrous oxide (N2O) have started to drift since ~2010. The paper also discusses the origins of this drift and work to ameliorate it in a new version of the MLS dataset.
Jerald R. Ziemke, Gordon J. Labow, Natalya A. Kramarova, Richard D. McPeters, Pawan K. Bhartia, Luke D. Oman, Stacey M. Frith, and David P. Haffner
Atmos. Meas. Tech., 14, 6407–6418, https://doi.org/10.5194/amt-14-6407-2021, https://doi.org/10.5194/amt-14-6407-2021, 2021
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Seasonal and interannual ozone profile climatologies are produced from combined MLS and MERRA-2 GMI ozone for the general public. Both climatologies extend from pole to pole at altitudes of 0–80 km (1 km spacing) for the time record from 1970 to 2018. These climatologies are important for use as a priori information in satellite ozone retrieval algorithms, as validation of other measured and model-simulated ozone, and in radiative transfer studies of the atmosphere.
Nora Mettig, Mark Weber, Alexei Rozanov, Carlo Arosio, John P. Burrows, Pepijn Veefkind, Anne M. Thompson, Richard Querel, Thierry Leblanc, Sophie Godin-Beekmann, Rigel Kivi, and Matthew B. Tully
Atmos. Meas. Tech., 14, 6057–6082, https://doi.org/10.5194/amt-14-6057-2021, https://doi.org/10.5194/amt-14-6057-2021, 2021
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TROPOMI is a nadir-viewing satellite that has observed global atmospheric trace gases at unprecedented spatial resolution since 2017. The retrieval of ozone profiles with high accuracy has been demonstrated using the TOPAS (Tikhonov regularised Ozone Profile retrievAl with SCIATRAN) algorithm and applying appropriate spectral corrections to TROPOMI UV data. Ozone profiles from TROPOMI were compared to ozonesonde and lidar profiles, showing an agreement to within 5 % in the stratosphere.
Hao Guo, Clare M. Flynn, Michael J. Prather, Sarah A. Strode, Stephen D. Steenrod, Louisa Emmons, Forrest Lacey, Jean-Francois Lamarque, Arlene M. Fiore, Gus Correa, Lee T. Murray, Glenn M. Wolfe, Jason M. St. Clair, Michelle Kim, John Crounse, Glenn Diskin, Joshua DiGangi, Bruce C. Daube, Roisin Commane, Kathryn McKain, Jeff Peischl, Thomas B. Ryerson, Chelsea Thompson, Thomas F. Hanisco, Donald Blake, Nicola J. Blake, Eric C. Apel, Rebecca S. Hornbrook, James W. Elkins, Eric J. Hintsa, Fred L. Moore, and Steven Wofsy
Atmos. Chem. Phys., 21, 13729–13746, https://doi.org/10.5194/acp-21-13729-2021, https://doi.org/10.5194/acp-21-13729-2021, 2021
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The NASA Atmospheric Tomography (ATom) mission built a climatology of the chemical composition of tropospheric air parcels throughout the middle of the Pacific and Atlantic oceans. The level of detail allows us to reconstruct the photochemical budgets of O3 and CH4 over these vast, remote regions. We find that most of the chemical heterogeneity is captured at the resolution used in current global chemistry models and that the majority of reactivity occurs in the
hottest20 % of parcels.
Sampa Das, Peter R. Colarco, Luke D. Oman, Ghassan Taha, and Omar Torres
Atmos. Chem. Phys., 21, 12069–12090, https://doi.org/10.5194/acp-21-12069-2021, https://doi.org/10.5194/acp-21-12069-2021, 2021
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Interactions of extreme fires with weather systems can produce towering smoke plumes that inject aerosols at very high altitudes (> 10 km). Three such major injections, largest at the time in terms of emitted aerosol mass, took place over British Columbia, Canada, in August 2017. We model the transport and impacts of injected aerosols on the radiation balance of the atmosphere. Our model results match the satellite-observed plume transport and residence time at these high altitudes very closely.
Jianfeng Li, Yuhang Wang, Ruixiong Zhang, Charles Smeltzer, Andrew Weinheimer, Jay Herman, K. Folkert Boersma, Edward A. Celarier, Russell W. Long, James J. Szykman, Ruben Delgado, Anne M. Thompson, Travis N. Knepp, Lok N. Lamsal, Scott J. Janz, Matthew G. Kowalewski, Xiong Liu, and Caroline R. Nowlan
Atmos. Chem. Phys., 21, 11133–11160, https://doi.org/10.5194/acp-21-11133-2021, https://doi.org/10.5194/acp-21-11133-2021, 2021
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Comprehensive evaluations of simulated diurnal cycles of NO2 and NOy concentrations, vertical profiles, and tropospheric vertical column densities at two different resolutions with various measurements during the DISCOVER-AQ 2011 campaign show potential distribution biases of NOx emissions in the National Emissions Inventory 2011 at both 36 and 4 km resolutions, providing another possible explanation for the overestimation of model results.
Lily N. Zhang, Susan Solomon, Kane A. Stone, Jonathan D. Shanklin, Joshua D. Eveson, Steve Colwell, John P. Burrows, Mark Weber, Pieternel F. Levelt, Natalya A. Kramarova, and David P. Haffner
Atmos. Chem. Phys., 21, 9829–9838, https://doi.org/10.5194/acp-21-9829-2021, https://doi.org/10.5194/acp-21-9829-2021, 2021
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In the 1980s, measurements at the British Antarctic Survey station in Halley, Antarctica, led to the discovery of the ozone hole. The Halley total ozone record continues to be uniquely valuable for studies of long-term changes in Antarctic ozone. Environmental conditions in 2017 forced a temporary cessation of operations, leading to a gap in the historic record. We develop and test a method for filling in the Halley record using satellite data and find evidence to further support ozone recovery.
Michaela I. Hegglin, Susann Tegtmeier, John Anderson, Adam E. Bourassa, Samuel Brohede, Doug Degenstein, Lucien Froidevaux, Bernd Funke, John Gille, Yasuko Kasai, Erkki T. Kyrölä, Jerry Lumpe, Donal Murtagh, Jessica L. Neu, Kristell Pérot, Ellis E. Remsberg, Alexei Rozanov, Matthew Toohey, Joachim Urban, Thomas von Clarmann, Kaley A. Walker, Hsiang-Jui Wang, Carlo Arosio, Robert Damadeo, Ryan A. Fuller, Gretchen Lingenfelser, Christopher McLinden, Diane Pendlebury, Chris Roth, Niall J. Ryan, Christopher Sioris, Lesley Smith, and Katja Weigel
Earth Syst. Sci. Data, 13, 1855–1903, https://doi.org/10.5194/essd-13-1855-2021, https://doi.org/10.5194/essd-13-1855-2021, 2021
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An overview of the SPARC Data Initiative is presented, to date the most comprehensive assessment of stratospheric composition measurements spanning 1979–2018. Measurements of 26 chemical constituents obtained from an international suite of space-based limb sounders were compiled into vertically resolved, zonal monthly mean time series. The quality and consistency of these gridded datasets are then evaluated using a climatological validation approach and a range of diagnostics.
Viktoria F. Sofieva, Monika Szeląg, Johanna Tamminen, Erkki Kyrölä, Doug Degenstein, Chris Roth, Daniel Zawada, Alexei Rozanov, Carlo Arosio, John P. Burrows, Mark Weber, Alexandra Laeng, Gabriele P. Stiller, Thomas von Clarmann, Lucien Froidevaux, Nathaniel Livesey, Michel van Roozendael, and Christian Retscher
Atmos. Chem. Phys., 21, 6707–6720, https://doi.org/10.5194/acp-21-6707-2021, https://doi.org/10.5194/acp-21-6707-2021, 2021
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The MErged GRIdded Dataset of Ozone Profiles is a long-term (2001–2018) stratospheric ozone profile climate data record with resolved longitudinal structure that combines the data from six limb satellite instruments. The dataset can be used for various analyses, some of which are discussed in the paper. In particular, regionally and vertically resolved ozone trends are evaluated, including trends in the polar regions.
Holger Vömel, Mack Goodstein, Laura Tudor, Jacquelyn Witte, Željka Fuchs-Stone, Stipo Sentić, David Raymond, Jose Martinez-Claros, Ana Juračić, Vijit Maithel, and Justin W. Whitaker
Earth Syst. Sci. Data, 13, 1107–1117, https://doi.org/10.5194/essd-13-1107-2021, https://doi.org/10.5194/essd-13-1107-2021, 2021
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We provide an extensive data set of in situ vertical profile observations for pressure, temperature, humidity, and winds from 648 NCAR NRD41 dropsondes during the Organization of Tropical East Pacific Convection (OTREC) field campaign. The measurements were taken during 22 flights of the NSF/NCAR G-V research aircraft in August and September 2019 over the eastern Pacific Ocean and the Caribbean Sea. The data allow a detailed study of atmospheric dynamics and convection over the tropical ocean.
Youhua Tang, Huisheng Bian, Zhining Tao, Luke D. Oman, Daniel Tong, Pius Lee, Patrick C. Campbell, Barry Baker, Cheng-Hsuan Lu, Li Pan, Jun Wang, Jeffery McQueen, and Ivanka Stajner
Atmos. Chem. Phys., 21, 2527–2550, https://doi.org/10.5194/acp-21-2527-2021, https://doi.org/10.5194/acp-21-2527-2021, 2021
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Chemical lateral boundary condition (CLBC) impact is essential for regional air quality prediction during intrusion events. We present a model mapping Goddard Earth Observing System (GEOS) to Community Multi-scale Air Quality (CMAQ) CB05–AERO6 (Carbon Bond 5; version 6 of the aerosol module) species. Influence depends on distance from the inflow boundary and species and their regional characteristics. We use aerosol optical thickness to derive CLBCs, achieving reasonable prediction.
Seidai Nara, Tomohiro O. Sato, Takayoshi Yamada, Tamaki Fujinawa, Kota Kuribayashi, Takeshi Manabe, Lucien Froidevaux, Nathaniel J. Livesey, Kaley A. Walker, Jian Xu, Franz Schreier, Yvan J. Orsolini, Varavut Limpasuvan, Nario Kuno, and Yasuko Kasai
Atmos. Meas. Tech., 13, 6837–6852, https://doi.org/10.5194/amt-13-6837-2020, https://doi.org/10.5194/amt-13-6837-2020, 2020
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In the atmosphere, more than 80 % of chlorine compounds are anthropogenic. Hydrogen chloride (HCl), the main stratospheric chlorine reservoir, is useful to estimate the total budget of the atmospheric chlorine compounds. We report, for the first time, the HCl vertical distribution from the middle troposphere to the lower thermosphere using a high-sensitivity SMILES measurement; the data quality is quantified by comparisons with other measurements and via theoretical error analysis.
Omar Torres, Hiren Jethva, Changwoo Ahn, Glen Jaross, and Diego G. Loyola
Atmos. Meas. Tech., 13, 6789–6806, https://doi.org/10.5194/amt-13-6789-2020, https://doi.org/10.5194/amt-13-6789-2020, 2020
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TROPOMI measures the quantity of small suspended particles (aerosols). We describe initial results of aerosol measurements using a NASA algorithm that retrieves the UV aerosol index, aerosol optical depth, and single-scattering albedo. An evaluation of derived products using sun-photometer observations shows close agreement. We also use these results to discuss important biomass burning and wildfire events around the world that got the attention of scientists and news media alike.
Yuanhong Zhao, Marielle Saunois, Philippe Bousquet, Xin Lin, Antoine Berchet, Michaela I. Hegglin, Josep G. Canadell, Robert B. Jackson, Makoto Deushi, Patrick Jöckel, Douglas Kinnison, Ole Kirner, Sarah Strode, Simone Tilmes, Edward J. Dlugokencky, and Bo Zheng
Atmos. Chem. Phys., 20, 13011–13022, https://doi.org/10.5194/acp-20-13011-2020, https://doi.org/10.5194/acp-20-13011-2020, 2020
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Decadal trends and variations in OH are critical for understanding atmospheric CH4 evolution. We quantify the impacts of OH trends and variations on the CH4 budget by conducting CH4 inversions on a decadal scale with an ensemble of OH fields. We find the negative OH anomalies due to enhanced fires can reduce the optimized CH4 emissions by up to 10 Tg yr−1 during El Niño years and the positive OH trend from 1986 to 2010 results in a ∼ 23 Tg yr−1 additional increase in optimized CH4 emissions.
Clark J. Weaver, Pawan K. Bhartia, Dong L. Wu, Gordon J. Labow, and David E. Haffner
Atmos. Meas. Tech., 13, 5715–5723, https://doi.org/10.5194/amt-13-5715-2020, https://doi.org/10.5194/amt-13-5715-2020, 2020
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Currently, we do not know whether clouds will accelerate or moderate climate. We look to the past and ask whether cloudiness has changed over the last 4 decades. Using a suite of nine satellite instruments, we need to ensure that the first satellite, which was launched in 1980 and died in 1991, observed the same measurement as the eight other satellite instruments used in the record. If the instruments were measuring length and observing a 1.00 m long stick, they would all see 0.99 to 1.01 m.
Holger Vömel, Herman G. J. Smit, David Tarasick, Bryan Johnson, Samuel J. Oltmans, Henry Selkirk, Anne M. Thompson, Ryan M. Stauffer, Jacquelyn C. Witte, Jonathan Davies, Roeland van Malderen, Gary A. Morris, Tatsumi Nakano, and Rene Stübi
Atmos. Meas. Tech., 13, 5667–5680, https://doi.org/10.5194/amt-13-5667-2020, https://doi.org/10.5194/amt-13-5667-2020, 2020
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The time response of electrochemical concentration cell (ECC) ozonesondes points to at least two distinct reaction pathways with time constants of approximately 20 s and 25 min. Properly considering these time constants eliminates the need for a poorly defined "background" and allows reducing ad hoc corrections based on laboratory tests. This reduces the uncertainty of ECC ozonesonde measurements throughout the profile and especially in regions of low ozone and strong gradients of ozone.
Ilann Bourgeois, Jeff Peischl, Chelsea R. Thompson, Kenneth C. Aikin, Teresa Campos, Hannah Clark, Róisín Commane, Bruce Daube, Glenn W. Diskin, James W. Elkins, Ru-Shan Gao, Audrey Gaudel, Eric J. Hintsa, Bryan J. Johnson, Rigel Kivi, Kathryn McKain, Fred L. Moore, David D. Parrish, Richard Querel, Eric Ray, Ricardo Sánchez, Colm Sweeney, David W. Tarasick, Anne M. Thompson, Valérie Thouret, Jacquelyn C. Witte, Steve C. Wofsy, and Thomas B. Ryerson
Atmos. Chem. Phys., 20, 10611–10635, https://doi.org/10.5194/acp-20-10611-2020, https://doi.org/10.5194/acp-20-10611-2020, 2020
Thomas von Clarmann, Douglas A. Degenstein, Nathaniel J. Livesey, Stefan Bender, Amy Braverman, André Butz, Steven Compernolle, Robert Damadeo, Seth Dueck, Patrick Eriksson, Bernd Funke, Margaret C. Johnson, Yasuko Kasai, Arno Keppens, Anne Kleinert, Natalya A. Kramarova, Alexandra Laeng, Bavo Langerock, Vivienne H. Payne, Alexei Rozanov, Tomohiro O. Sato, Matthias Schneider, Patrick Sheese, Viktoria Sofieva, Gabriele P. Stiller, Christian von Savigny, and Daniel Zawada
Atmos. Meas. Tech., 13, 4393–4436, https://doi.org/10.5194/amt-13-4393-2020, https://doi.org/10.5194/amt-13-4393-2020, 2020
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Remote sensing of atmospheric state variables typically relies on the inverse solution of the radiative transfer equation. An adequately characterized retrieval provides information on the uncertainties of the estimated state variables as well as on how any constraint or a priori assumption affects the estimate. This paper summarizes related techniques and provides recommendations for unified error reporting.
Jay Herman, Alexander Cede, Liang Huang, Jerald Ziemke, Omar Torres, Nickolay Krotkov, Matthew Kowalewski, and Karin Blank
Atmos. Chem. Phys., 20, 8351–8380, https://doi.org/10.5194/acp-20-8351-2020, https://doi.org/10.5194/acp-20-8351-2020, 2020
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The amount of erythemal irradiance reaching the Earth's surface has been calculated from ozone, aerosol, and reflectivity data obtained from OMI and DSCOVR/EPIC satellite instruments showing areas with high levels of solar UV radiation. Changes in erythemal irradiance, cloud transmission, aerosol transmission, and ozone absorption have been estimated for 14 years 2005–2018 in units of percent per year for 191 locations, mostly large cities, and from EPIC for the entire illuminated Earth.
Sarah A. Strode, James S. Wang, Michael Manyin, Bryan Duncan, Ryan Hossaini, Christoph A. Keller, Sylvia E. Michel, and James W. C. White
Atmos. Chem. Phys., 20, 8405–8419, https://doi.org/10.5194/acp-20-8405-2020, https://doi.org/10.5194/acp-20-8405-2020, 2020
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The 13C : 12C isotopic ratio in methane (CH4) provides information about CH4 sources, but loss of CH4 by reaction with OH and chlorine (Cl) also affects this ratio. Tropospheric Cl provides a small and uncertain sink for CH4 but has a large effect on its isotopic ratio. We use the GEOS model with several different Cl fields to test the sensitivity of methane's isotopic composition to tropospheric Cl. Cl affects the global mean, hemispheric gradient, and seasonal cycle of the isotopic ratio.
Daniele Visioni, Giovanni Pitari, Vincenzo Rizi, Marco Iarlori, Irene Cionni, Ilaria Quaglia, Hideharu Akiyoshi, Slimane Bekki, Neal Butchart, Martin Chipperfield, Makoto Deushi, Sandip S. Dhomse, Rolando Garcia, Patrick Joeckel, Douglas Kinnison, Jean-François Lamarque, Marion Marchand, Martine Michou, Olaf Morgenstern, Tatsuya Nagashima, Fiona M. O'Connor, Luke D. Oman, David Plummer, Eugene Rozanov, David Saint-Martin, Robyn Schofield, John Scinocca, Andrea Stenke, Kane Stone, Kengo Sudo, Taichu Y. Tanaka, Simone Tilmes, Holger Tost, Yousuke Yamashita, and Guang Zeng
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2020-525, https://doi.org/10.5194/acp-2020-525, 2020
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In this work we analyse the trend in ozone profiles taken at L'Aquila (Italy, 42.4° N) for seventeen years, between 2000 and 2016 and compare them against already available measured ozone trends. We try to understand and explain the observed trends at various heights in light of the simulations from seventeen different model, highlighting the contribution of changes in circulation and chemical ozone loss during this time period.
Zhong Chen, Pawan K. Bhartia, Omar Torres, Glen Jaross, Robert Loughman, Matthew DeLand, Peter Colarco, Robert Damadeo, and Ghassan Taha
Atmos. Meas. Tech., 13, 3471–3485, https://doi.org/10.5194/amt-13-3471-2020, https://doi.org/10.5194/amt-13-3471-2020, 2020
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The scope of the paper is the evaluation of stratospheric aerosols derived from the OMPS/LP instrument via comparison with independent datasets from the SAGE III/ISS instrument. Results show very good agreement for extinction profiles between an altitude of 19 and 27 km, to within ±25 %, and show systematic differences (LP-SAGE III/ISS) above 28 km and below 19 km (greater than ±25 %).
Monika E. Szeląg, Viktoria F. Sofieva, Doug Degenstein, Chris Roth, Sean Davis, and Lucien Froidevaux
Atmos. Chem. Phys., 20, 7035–7047, https://doi.org/10.5194/acp-20-7035-2020, https://doi.org/10.5194/acp-20-7035-2020, 2020
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We analyze seasonal dependence of stratospheric ozone trends over 2000–2018. We demonstrate that the mid-latitude upper stratospheric ozone recovery maximizes during local winters and equinoxes. In the tropics, a very strong seasonal dependence of ozone trends is observed at all altitudes. We found hemispheric asymmetry of summertime ozone trend patterns below 35 km. The seasonal dependence of ozone trends and stratospheric temperature trends shows a clear inter-relation of the trend patterns.
Marta Abalos, Clara Orbe, Douglas E. Kinnison, David Plummer, Luke D. Oman, Patrick Jöckel, Olaf Morgenstern, Rolando R. Garcia, Guang Zeng, Kane A. Stone, and Martin Dameris
Atmos. Chem. Phys., 20, 6883–6901, https://doi.org/10.5194/acp-20-6883-2020, https://doi.org/10.5194/acp-20-6883-2020, 2020
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A set of state-of-the art chemistry–climate models is used to examine future changes in downward transport from the stratosphere, a key contributor to tropospheric ozone. The acceleration of the stratospheric circulation results in increased stratosphere-to-troposphere transport. In the subtropics, downward advection into the troposphere is enhanced due to climate change. At higher latitudes, the ozone reservoir above the tropopause is enlarged due to the stronger circulation and ozone recovery.
Junhua Liu, Jose M. Rodriguez, Luke D. Oman, Anne R. Douglass, Mark A. Olsen, and Lu Hu
Atmos. Chem. Phys., 20, 6417–6433, https://doi.org/10.5194/acp-20-6417-2020, https://doi.org/10.5194/acp-20-6417-2020, 2020
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Our paper quantifies and identifies the importance of stratospheric ozone influence on the tropospheric ozone IAV in Northern Hemisphere mid-high latitudes. Our analysis provides an in-depth understanding of how 3-D dynamics influences the O3 redistribution in the troposphere. These findings are particularly important considering the potential changes in these dynamical conditions in the future as a result of climate change
Stacey M. Frith, Pawan K. Bhartia, Luke D. Oman, Natalya A. Kramarova, Richard D. McPeters, and Gordon J. Labow
Atmos. Meas. Tech., 13, 2733–2749, https://doi.org/10.5194/amt-13-2733-2020, https://doi.org/10.5194/amt-13-2733-2020, 2020
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We use the NASA GEOS-GMI chemistry climate model to construct a climatology of stratospheric ozone diurnal variations as a function of latitude, pressure and month, which can be used in a variety of data analysis tasks involving ozone observations made at different times of the day. The climatology compares well with previous modeling simulations and available observations, and to the authors' knowledge is the first characterization of the diurnal cycle available for general ozone data analyses.
Melanie Coldewey-Egbers, Diego G. Loyola, Gordon Labow, and Stacey M. Frith
Atmos. Meas. Tech., 13, 1633–1654, https://doi.org/10.5194/amt-13-1633-2020, https://doi.org/10.5194/amt-13-1633-2020, 2020
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We compare total ozone columns from the satellite-based GOME-type Total Ozone Essential Climate Variable record and the adjusted Modern Era Retrospective Analysis for Research and Applications version 2 reanalysis during their overlap period from 1995 to 2018. Ozone columns and anomalies show a very good agreement in terms of spatial and temporal patterns. In the tropics the interannual variability is assessed by means of an EOF analysis and both data records show a remarkable consistency.
Ernest Nyaku, Robert Loughman, Pawan K. Bhartia, Terry Deshler, Zhong Chen, and Peter R. Colarco
Atmos. Meas. Tech., 13, 1071–1087, https://doi.org/10.5194/amt-13-1071-2020, https://doi.org/10.5194/amt-13-1071-2020, 2020
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This paper shows the importance of the nature of the aerosol phase function used in the retrieval of the stratospheric aerosol extinction from limb scattering measurements. The aerosol phase function is derived from the parameters using either a unimodal lognormal or gamma aerosol size distribution. These two distributions were fitted to the same aerosol concentration measurements at two altitudes, and depending on the nature of the measurements, each distribution shows its strengths.
Julie M. Nicely, Bryan N. Duncan, Thomas F. Hanisco, Glenn M. Wolfe, Ross J. Salawitch, Makoto Deushi, Amund S. Haslerud, Patrick Jöckel, Béatrice Josse, Douglas E. Kinnison, Andrew Klekociuk, Michael E. Manyin, Virginie Marécal, Olaf Morgenstern, Lee T. Murray, Gunnar Myhre, Luke D. Oman, Giovanni Pitari, Andrea Pozzer, Ilaria Quaglia, Laura E. Revell, Eugene Rozanov, Andrea Stenke, Kane Stone, Susan Strahan, Simone Tilmes, Holger Tost, Daniel M. Westervelt, and Guang Zeng
Atmos. Chem. Phys., 20, 1341–1361, https://doi.org/10.5194/acp-20-1341-2020, https://doi.org/10.5194/acp-20-1341-2020, 2020
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Differences in methane lifetime among global models are large and poorly understood. We use a neural network method and simulations from the Chemistry Climate Model Initiative to quantify the factors influencing methane lifetime spread among models and variations over time. UV photolysis, tropospheric ozone, and nitrogen oxides drive large model differences, while the same factors plus specific humidity contribute to a decreasing trend in methane lifetime between 1980 and 2015.
Le Kuai, Kevin W. Bowman, Kazuyuki Miyazaki, Makoto Deushi, Laura Revell, Eugene Rozanov, Fabien Paulot, Sarah Strode, Andrew Conley, Jean-François Lamarque, Patrick Jöckel, David A. Plummer, Luke D. Oman, Helen Worden, Susan Kulawik, David Paynter, Andrea Stenke, and Markus Kunze
Atmos. Chem. Phys., 20, 281–301, https://doi.org/10.5194/acp-20-281-2020, https://doi.org/10.5194/acp-20-281-2020, 2020
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The tropospheric ozone increase from pre-industrial to the present day leads to a radiative forcing. The top-of-atmosphere outgoing fluxes at the ozone band are controlled by ozone, water vapor, and temperature. We demonstrate a method to attribute the models’ flux biases to these key players using satellite-constrained instantaneous radiative kernels. The largest spread between models is found in the tropics, mainly driven by ozone and then water vapor.
Yuanhong Zhao, Marielle Saunois, Philippe Bousquet, Xin Lin, Antoine Berchet, Michaela I. Hegglin, Josep G. Canadell, Robert B. Jackson, Didier A. Hauglustaine, Sophie Szopa, Ann R. Stavert, Nathan Luke Abraham, Alex T. Archibald, Slimane Bekki, Makoto Deushi, Patrick Jöckel, Béatrice Josse, Douglas Kinnison, Ole Kirner, Virginie Marécal, Fiona M. O'Connor, David A. Plummer, Laura E. Revell, Eugene Rozanov, Andrea Stenke, Sarah Strode, Simone Tilmes, Edward J. Dlugokencky, and Bo Zheng
Atmos. Chem. Phys., 19, 13701–13723, https://doi.org/10.5194/acp-19-13701-2019, https://doi.org/10.5194/acp-19-13701-2019, 2019
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The role of hydroxyl radical changes in methane trends is debated, hindering our understanding of the methane cycle. This study quantifies how uncertainties in the hydroxyl radical may influence methane abundance in the atmosphere based on the inter-model comparison of hydroxyl radical fields and model simulations of CH4 abundance with different hydroxyl radical scenarios during 2000–2016. We show that hydroxyl radical changes could contribute up to 54 % of model-simulated methane biases.
William T. Ball, Justin Alsing, Johannes Staehelin, Sean M. Davis, Lucien Froidevaux, and Thomas Peter
Atmos. Chem. Phys., 19, 12731–12748, https://doi.org/10.5194/acp-19-12731-2019, https://doi.org/10.5194/acp-19-12731-2019, 2019
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We analyse long-term stratospheric ozone (60° S–60° N) trends over the 1985–2018 period. Previous work has suggested that lower stratosphere ozone declined over 1998–2016. We demonstrate that a large ozone upsurge in 2017 is likely related to QBO variability, but that lower stratospheric ozone trends likely remain lower in 2018 than in 1998. Tropical stratospheric ozone (30° S–30° N) shows highly probable decreases in both the lower stratosphere and in the integrated stratospheric ozone layer.
Bradford L. Fisher, Nickolay A. Krotkov, Pawan K. Bhartia, Can Li, Simon A. Carn, Eric Hughes, and Peter J. T. Leonard
Atmos. Meas. Tech., 12, 5137–5153, https://doi.org/10.5194/amt-12-5137-2019, https://doi.org/10.5194/amt-12-5137-2019, 2019
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This article describes a new discrete wavelength algorithm, MS_SO2, which has been used operationally to retrieve global daily volcanic SO2 vertical column densities and the UV volcanic ash index from the Total Ozone Mapping Spectrometer (TOMS) data collected by NASA’s Nimbus-7 satellite from 1978 to 1991. We examine the sensitivity of the algorithm to the detection of SO2, evaluate potential sources of error and compare results from MS_SO2 with the Principal Component Analysis (PCA) algorithm.
Kévin Lamy, Thierry Portafaix, Béatrice Josse, Colette Brogniez, Sophie Godin-Beekmann, Hassan Bencherif, Laura Revell, Hideharu Akiyoshi, Slimane Bekki, Michaela I. Hegglin, Patrick Jöckel, Oliver Kirner, Ben Liley, Virginie Marecal, Olaf Morgenstern, Andrea Stenke, Guang Zeng, N. Luke Abraham, Alexander T. Archibald, Neil Butchart, Martyn P. Chipperfield, Glauco Di Genova, Makoto Deushi, Sandip S. Dhomse, Rong-Ming Hu, Douglas Kinnison, Michael Kotkamp, Richard McKenzie, Martine Michou, Fiona M. O'Connor, Luke D. Oman, Giovanni Pitari, David A. Plummer, John A. Pyle, Eugene Rozanov, David Saint-Martin, Kengo Sudo, Taichu Y. Tanaka, Daniele Visioni, and Kohei Yoshida
Atmos. Chem. Phys., 19, 10087–10110, https://doi.org/10.5194/acp-19-10087-2019, https://doi.org/10.5194/acp-19-10087-2019, 2019
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In this study, we simulate the ultraviolet radiation evolution during the 21st century on Earth's surface using the output from several numerical models which participated in the Chemistry-Climate Model Initiative. We present four possible futures which depend on greenhouse gases emissions. The role of ozone-depleting substances, greenhouse gases and aerosols are investigated. Our results emphasize the important role of aerosols for future ultraviolet radiation in the Northern Hemisphere.
Matthew T. DeLand and Gary E. Thomas
Atmos. Chem. Phys., 19, 7913–7925, https://doi.org/10.5194/acp-19-7913-2019, https://doi.org/10.5194/acp-19-7913-2019, 2019
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We have extended our 40-year satellite data record of polar mesospheric cloud (PMC) behavior by adding data from a new instrument. Long-term trends in PMC ice water content derived from this record are smaller since 1998 compared to the first part of our data record. The PMC response to solar activity has decreased in the Northern Hemisphere but increased in the Southern Hemisphere, for reasons that are not understood.
John T. Sullivan, Thomas J. McGee, Ryan M. Stauffer, Anne M. Thompson, Andrew Weinheimer, Christoph Knote, Scott Janz, Armin Wisthaler, Russell Long, James Szykman, Jinsoo Park, Youngjae Lee, Saewung Kim, Daun Jeong, Dianne Sanchez, Laurence Twigg, Grant Sumnicht, Travis Knepp, and Jason R. Schroeder
Atmos. Chem. Phys., 19, 5051–5067, https://doi.org/10.5194/acp-19-5051-2019, https://doi.org/10.5194/acp-19-5051-2019, 2019
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During the May–June 2016 International Cooperative Air Quality Field Study in Korea (KORUS-AQ), pollution reached the remote Taehwa Research Forest (TRF) site. Two case studies are examined and observations clearly identify TRF and the surrounding rural areas as long-term receptor sites for severe urban pollution events. In summary, domestic emissions may be causing more pollution than by transboundary pathways, which have been historically believed to be the major source of air pollution.
Kostas Eleftheratos, Christos S. Zerefos, Dimitris S. Balis, Maria-Elissavet Koukouli, John Kapsomenakis, Diego G. Loyola, Pieter Valks, Melanie Coldewey-Egbers, Christophe Lerot, Stacey M. Frith, Amund S. Haslerud, Ivar S. A. Isaksen, and Seppo Hassinen
Atmos. Meas. Tech., 12, 987–1011, https://doi.org/10.5194/amt-12-987-2019, https://doi.org/10.5194/amt-12-987-2019, 2019
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We examine the ability of GOME-2A total ozone data to capture variability related to known natural oscillations, such as the QBO, ENSO and NAO, with respect to other satellite datasets, ground-based data, and chemical transport model simulations. The analysis is based on the GOME-2 satellite total ozone columns for the period 2007–2016 which form part of the operational EUMETSAT AC SAF GOME-2 MetOp A GDP4.8 latest data product.
Richard McPeters, Stacey Frith, Natalya Kramarova, Jerry Ziemke, and Gordon Labow
Atmos. Meas. Tech., 12, 977–985, https://doi.org/10.5194/amt-12-977-2019, https://doi.org/10.5194/amt-12-977-2019, 2019
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A version 2 processing of data from the OMPS nadir ozone mapper and nadir ozone profiler on Suomi NPP has now been completed. Total column ozone data from the OMPS nadir mapper now agree with data from the SBUV/2 instrument on NOAA 19, with a zonal average bias of −0.2 % over the 60° S to 60° N latitude zone. For the profile retrieval, zonal average ozone in the upper stratosphere (between 2.5 and 4 hPa) agrees with that from NOAA 19 within ±3 % and an average bias of −1.1 %.
Roland Eichinger, Simone Dietmüller, Hella Garny, Petr Šácha, Thomas Birner, Harald Bönisch, Giovanni Pitari, Daniele Visioni, Andrea Stenke, Eugene Rozanov, Laura Revell, David A. Plummer, Patrick Jöckel, Luke Oman, Makoto Deushi, Douglas E. Kinnison, Rolando Garcia, Olaf Morgenstern, Guang Zeng, Kane Adam Stone, and Robyn Schofield
Atmos. Chem. Phys., 19, 921–940, https://doi.org/10.5194/acp-19-921-2019, https://doi.org/10.5194/acp-19-921-2019, 2019
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To shed more light upon the changes in stratospheric circulation in the 21st century, climate projection simulations of 10 state-of-the-art global climate models, spanning from 1960 to 2100, are analyzed. The study shows that in addition to changes in transport, mixing also plays an important role in stratospheric circulation and that the properties of mixing vary over time. Furthermore, the influence of mixing is quantified and a dynamical framework is provided to understand the changes.
Zhong Chen, Pawan K. Bhartia, Robert Loughman, Peter Colarco, and Matthew DeLand
Atmos. Meas. Tech., 11, 6495–6509, https://doi.org/10.5194/amt-11-6495-2018, https://doi.org/10.5194/amt-11-6495-2018, 2018
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We describe the derivation of an improved aerosol size distribution (ASD) for the OMPS/LP retrieval algorithm. The new ASD uses a gamma function distribution that is derived from CARMA-calculated results. The new ASD also explains the spectral dependence of LP-measured radiances well. Initial comparisons with collocated extinction profiles retrieved at 676 nm from the SAGE III/ISS instrument show a significant improvement in agreement for the LP retrievals.
Samuel R. Hall, Kirk Ullmann, Michael J. Prather, Clare M. Flynn, Lee T. Murray, Arlene M. Fiore, Gustavo Correa, Sarah A. Strode, Stephen D. Steenrod, Jean-Francois Lamarque, Jonathan Guth, Béatrice Josse, Johannes Flemming, Vincent Huijnen, N. Luke Abraham, and Alex T. Archibald
Atmos. Chem. Phys., 18, 16809–16828, https://doi.org/10.5194/acp-18-16809-2018, https://doi.org/10.5194/acp-18-16809-2018, 2018
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Photolysis (J rates) initiates and drives atmospheric chemistry, and Js are perturbed by factors of 2 by clouds. The NASA Atmospheric Tomography (ATom) Mission provides the first comprehensive observations on how clouds perturb Js through the remote Pacific and Atlantic basins. We compare these cloud-perturbation J statistics with those from nine global chemistry models. While basic patterns agree, there is a large spread across models, and all lack some basic features of the observations.
Laura E. Revell, Andrea Stenke, Fiona Tummon, Aryeh Feinberg, Eugene Rozanov, Thomas Peter, N. Luke Abraham, Hideharu Akiyoshi, Alexander T. Archibald, Neal Butchart, Makoto Deushi, Patrick Jöckel, Douglas Kinnison, Martine Michou, Olaf Morgenstern, Fiona M. O'Connor, Luke D. Oman, Giovanni Pitari, David A. Plummer, Robyn Schofield, Kane Stone, Simone Tilmes, Daniele Visioni, Yousuke Yamashita, and Guang Zeng
Atmos. Chem. Phys., 18, 16155–16172, https://doi.org/10.5194/acp-18-16155-2018, https://doi.org/10.5194/acp-18-16155-2018, 2018
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Global models such as those participating in the Chemistry-Climate Model Initiative (CCMI) consistently simulate biases in tropospheric ozone compared with observations. We performed an advanced statistical analysis with one of the CCMI models to understand the cause of the bias. We found that emissions of ozone precursor gases are the dominant driver of the bias, implying either that the emissions are too large, or that the way in which the model handles emissions needs to be improved.
Tracey Leah Laban, Pieter Gideon van Zyl, Johan Paul Beukes, Ville Vakkari, Kerneels Jaars, Nadine Borduas-Dedekind, Miroslav Josipovic, Anne Mee Thompson, Markku Kulmala, and Lauri Laakso
Atmos. Chem. Phys., 18, 15491–15514, https://doi.org/10.5194/acp-18-15491-2018, https://doi.org/10.5194/acp-18-15491-2018, 2018
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Surface O3 was measured at four sites in the north-eastern interior of South Africa, which revealed that O3 is a regional problem in continental South Africa, with elevated O3 levels found at rural background and industrial sites. Increased O3 concentrations were associated with high CO levels predominantly related to regional biomass burning, while the O3 production regime was established to be predominantly VOC limited. Increased O3 is associated with strong seasonality of precursor sources.
Dejian Fu, Susan S. Kulawik, Kazuyuki Miyazaki, Kevin W. Bowman, John R. Worden, Annmarie Eldering, Nathaniel J. Livesey, Joao Teixeira, Fredrick W. Irion, Robert L. Herman, Gregory B. Osterman, Xiong Liu, Pieternel F. Levelt, Anne M. Thompson, and Ming Luo
Atmos. Meas. Tech., 11, 5587–5605, https://doi.org/10.5194/amt-11-5587-2018, https://doi.org/10.5194/amt-11-5587-2018, 2018
Blanca Ayarzagüena, Lorenzo M. Polvani, Ulrike Langematz, Hideharu Akiyoshi, Slimane Bekki, Neal Butchart, Martin Dameris, Makoto Deushi, Steven C. Hardiman, Patrick Jöckel, Andrew Klekociuk, Marion Marchand, Martine Michou, Olaf Morgenstern, Fiona M. O'Connor, Luke D. Oman, David A. Plummer, Laura Revell, Eugene Rozanov, David Saint-Martin, John Scinocca, Andrea Stenke, Kane Stone, Yousuke Yamashita, Kohei Yoshida, and Guang Zeng
Atmos. Chem. Phys., 18, 11277–11287, https://doi.org/10.5194/acp-18-11277-2018, https://doi.org/10.5194/acp-18-11277-2018, 2018
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Stratospheric sudden warmings (SSWs) are natural major disruptions of the polar stratospheric circulation that also affect surface weather. In the literature there are conflicting claims as to whether SSWs will change in the future. The confusion comes from studies using different models and methods. Here we settle the question by analysing 12 models with a consistent methodology, to show that no robust changes in frequency and other features are expected over the 21st century.
Alexandra Laeng, Ellen Eckert, Thomas von Clarmann, Michael Kiefer, Daan Hubert, Gabriele Stiller, Norbert Glatthor, Manuel López-Puertas, Bernd Funke, Udo Grabowski, Johannes Plieninger, Sylvia Kellmann, Andrea Linden, Stefan Lossow, Arne Babenhauserheide, Lucien Froidevaux, and Kaley Walker
Atmos. Meas. Tech., 11, 4693–4705, https://doi.org/10.5194/amt-11-4693-2018, https://doi.org/10.5194/amt-11-4693-2018, 2018
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MIPAS was an IR limb emission spectrometer on the Envisat platform. From 2002 to 2012, it performed pole-to-pole measurements of ozone during day and night. ESA recently released the new version 7 of Level 1 MIPAS spectra, which is expected to reduce the long-term drift of the MIPAS Level 2 data. We evaluate the long-term stability of ozone Level 2 data from the KIT IMK processor. Our results indicate that MIPAS data are now even more suited for trend studies, alone or as part of merged data.
Wenfu Tang, Avelino F. Arellano, Joshua P. DiGangi, Yonghoon Choi, Glenn S. Diskin, Anna Agustí-Panareda, Mark Parrington, Sebastien Massart, Benjamin Gaubert, Youngjae Lee, Danbi Kim, Jinsang Jung, Jinkyu Hong, Je-Woo Hong, Yugo Kanaya, Mindo Lee, Ryan M. Stauffer, Anne M. Thompson, James H. Flynn, and Jung-Hun Woo
Atmos. Chem. Phys., 18, 11007–11030, https://doi.org/10.5194/acp-18-11007-2018, https://doi.org/10.5194/acp-18-11007-2018, 2018
Sarah A. Strode, Junhua Liu, Leslie Lait, Róisín Commane, Bruce Daube, Steven Wofsy, Austin Conaty, Paul Newman, and Michael Prather
Atmos. Chem. Phys., 18, 10955–10971, https://doi.org/10.5194/acp-18-10955-2018, https://doi.org/10.5194/acp-18-10955-2018, 2018
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The GEOS-5 atmospheric model provided forecasts for the Atmospheric Tomography Mission (ATom). GEOS-5 shows skill in simulating the carbon monoxide (CO) measured in ATom-1. African fires contribute to high CO over the tropical Atlantic, but non-fire sources are the main contributors elsewhere. ATom aims to provide a chemical climatology, so we consider whether ATom-1 occurred during a typical summer month. Satellite observations suggest ATom-1 occurred in a clean but not exceptional month.
Jay Herman, Guoyong Wen, Alexander Marshak, Karin Blank, Liang Huang, Alexander Cede, Nader Abuhassan, and Matthew Kowalewski
Atmos. Meas. Tech., 11, 4373–4388, https://doi.org/10.5194/amt-11-4373-2018, https://doi.org/10.5194/amt-11-4373-2018, 2018
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The DSCOVR/EPIC instrument located near the Lagrange 1 Earth–Sun gravitational balance point is able to view the entire sunlit disk of the Earth. This means that during the eclipse of 21 August 2017 EPIC was able to see the region of totality and the much larger region of partial eclipse. Because of this, EPIC is able to measure the global reduction of reflected solar flux. For the wavelength range 388 to 780 nm, we estimated a 10 % reduction in reflected radiation.
Alexander Vasilkov, Eun-Su Yang, Sergey Marchenko, Wenhan Qin, Lok Lamsal, Joanna Joiner, Nickolay Krotkov, David Haffner, Pawan K. Bhartia, and Robert Spurr
Atmos. Meas. Tech., 11, 4093–4107, https://doi.org/10.5194/amt-11-4093-2018, https://doi.org/10.5194/amt-11-4093-2018, 2018
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We discuss a new cloud algorithm that retrieves effective cloud fraction and cloud altitude and pressure from the oxygen dimer absorption band at 477 nm. The algorithm accounts for how changes in the sun–satellite geometry affect the surface reflection. The cloud fraction and pressure are used as inputs to the OMI algorithm that retrieves a pollutant gas called nitrogen dioxide. Impacts of the application of the newly developed cloud algorithm on the OMI nitrogen dioxide retrieval are discussed.
Elpida Leventidou, Mark Weber, Kai-Uwe Eichmann, John P. Burrows, Klaus-Peter Heue, Anne M. Thompson, and Bryan J. Johnson
Atmos. Chem. Phys., 18, 9189–9205, https://doi.org/10.5194/acp-18-9189-2018, https://doi.org/10.5194/acp-18-9189-2018, 2018
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Three individual tropical tropospheric ozone (TTCO) datasets (1996–2015) retrieved with the convective-cloud differential method (Leventidou et al., 2016) have been harmonised in order to study the global and regional TTCO trends. The trends range between −4 to 4 DU per decade testing six different merging scenarios. No trend has been found for the global tropics using the preferred scenario. It is concluded that harmonisation is one of the major sources of uncertainty in the trend estimates.
Chance W. Sterling, Bryan J. Johnson, Samuel J. Oltmans, Herman G. J. Smit, Allen F. Jordan, Patrick D. Cullis, Emrys G. Hall, Anne M. Thompson, and Jacquelyn C. Witte
Atmos. Meas. Tech., 11, 3661–3687, https://doi.org/10.5194/amt-11-3661-2018, https://doi.org/10.5194/amt-11-3661-2018, 2018
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The electrochemical concentration cell ozonesonde is a balloon-borne instrument that measures ozone to an altitude of ~30 km. This work summarizes the National Oceanic and Atmospheric Administration's 50+ year, eight-site ozonesonde network history, the processing techniques utilized to account for instrumental changes, and the uncertainty of the measurement. The ozonesonde measurements were compared to satellite measurements and agreed well. This important data set is more useful and robust.
Sandip S. Dhomse, Douglas Kinnison, Martyn P. Chipperfield, Ross J. Salawitch, Irene Cionni, Michaela I. Hegglin, N. Luke Abraham, Hideharu Akiyoshi, Alex T. Archibald, Ewa M. Bednarz, Slimane Bekki, Peter Braesicke, Neal Butchart, Martin Dameris, Makoto Deushi, Stacey Frith, Steven C. Hardiman, Birgit Hassler, Larry W. Horowitz, Rong-Ming Hu, Patrick Jöckel, Beatrice Josse, Oliver Kirner, Stefanie Kremser, Ulrike Langematz, Jared Lewis, Marion Marchand, Meiyun Lin, Eva Mancini, Virginie Marécal, Martine Michou, Olaf Morgenstern, Fiona M. O'Connor, Luke Oman, Giovanni Pitari, David A. Plummer, John A. Pyle, Laura E. Revell, Eugene Rozanov, Robyn Schofield, Andrea Stenke, Kane Stone, Kengo Sudo, Simone Tilmes, Daniele Visioni, Yousuke Yamashita, and Guang Zeng
Atmos. Chem. Phys., 18, 8409–8438, https://doi.org/10.5194/acp-18-8409-2018, https://doi.org/10.5194/acp-18-8409-2018, 2018
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We analyse simulations from the Chemistry-Climate Model Initiative (CCMI) to estimate the return dates of the stratospheric ozone layer from depletion by anthropogenic chlorine and bromine. The simulations from 20 models project that global column ozone will return to 1980 values in 2047 (uncertainty range 2042–2052). Return dates in other regions vary depending on factors related to climate change and importance of chlorine and bromine. Column ozone in the tropics may continue to decline.
Clara Orbe, Huang Yang, Darryn W. Waugh, Guang Zeng, Olaf Morgenstern, Douglas E. Kinnison, Jean-Francois Lamarque, Simone Tilmes, David A. Plummer, John F. Scinocca, Beatrice Josse, Virginie Marecal, Patrick Jöckel, Luke D. Oman, Susan E. Strahan, Makoto Deushi, Taichu Y. Tanaka, Kohei Yoshida, Hideharu Akiyoshi, Yousuke Yamashita, Andreas Stenke, Laura Revell, Timofei Sukhodolov, Eugene Rozanov, Giovanni Pitari, Daniele Visioni, Kane A. Stone, Robyn Schofield, and Antara Banerjee
Atmos. Chem. Phys., 18, 7217–7235, https://doi.org/10.5194/acp-18-7217-2018, https://doi.org/10.5194/acp-18-7217-2018, 2018
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In this study we compare a few atmospheric transport properties among several numerical models that are used to study the influence of atmospheric chemistry on climate. We show that there are large differences among models in terms of the timescales that connect the Northern Hemisphere midlatitudes, where greenhouse gases and ozone-depleting substances are emitted, to the Southern Hemisphere. Our results may have important implications for how models represent atmospheric composition.
Natalya A. Kramarova, Pawan K. Bhartia, Glen Jaross, Leslie Moy, Philippe Xu, Zhong Chen, Matthew DeLand, Lucien Froidevaux, Nathaniel Livesey, Douglas Degenstein, Adam Bourassa, Kaley A. Walker, and Patrick Sheese
Atmos. Meas. Tech., 11, 2837–2861, https://doi.org/10.5194/amt-11-2837-2018, https://doi.org/10.5194/amt-11-2837-2018, 2018
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The Ozone Mapping and Profiler Suite (OMPS) Limb Profiler (LP) is a newly designed research sensor aiming to continue high vertical resolution ozone records from space-borne sensors. In summer 2017 all LP measurements were processed with the new version 2.5 algorithm. In this paper we provide a description of the key changes implemented in the new algorithm and evaluate the quality of ozone retrievals by comparing with independent satellite profile measurements (MLS, ACE-FTS and OSIRIS).
Simone Dietmüller, Roland Eichinger, Hella Garny, Thomas Birner, Harald Boenisch, Giovanni Pitari, Eva Mancini, Daniele Visioni, Andrea Stenke, Laura Revell, Eugene Rozanov, David A. Plummer, John Scinocca, Patrick Jöckel, Luke Oman, Makoto Deushi, Shibata Kiyotaka, Douglas E. Kinnison, Rolando Garcia, Olaf Morgenstern, Guang Zeng, Kane Adam Stone, and Robyn Schofield
Atmos. Chem. Phys., 18, 6699–6720, https://doi.org/10.5194/acp-18-6699-2018, https://doi.org/10.5194/acp-18-6699-2018, 2018
Omar Torres, Pawan K. Bhartia, Hiren Jethva, and Changwoo Ahn
Atmos. Meas. Tech., 11, 2701–2715, https://doi.org/10.5194/amt-11-2701-2018, https://doi.org/10.5194/amt-11-2701-2018, 2018
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Since about three years after the launch the Ozone Monitoring Instrument (OMI) on the EOS-Aura satellite, the sensor’s viewing capability has been affected by what is believed to be an internal obstruction that has reduced OMI’s spatial coverage. It currently affects about half of the instrument’s 60 viewing positions. In this work we carry out an analysis to assess the effect of the reduced spatial coverage on the monthly average values of retrieved parameters.
Christos Zerefos, John Kapsomenakis, Kostas Eleftheratos, Kleareti Tourpali, Irina Petropavlovskikh, Daan Hubert, Sophie Godin-Beekmann, Wolfgang Steinbrecht, Stacey Frith, Viktoria Sofieva, and Birgit Hassler
Atmos. Chem. Phys., 18, 6427–6440, https://doi.org/10.5194/acp-18-6427-2018, https://doi.org/10.5194/acp-18-6427-2018, 2018
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We point out the representativeness of single lidar stations for zonally averaged ozone profile variations in the middle/upper stratosphere. We examine the contribution of chemistry and natural proxies to ozone profile trends. Above 10 hPa an “inflection point” between 1997–99 marks the end of significant negative ozone trends, followed by a recent period of positive ozone change in 1998–2015. Below 15 hPa the pre-1998 negative ozone trends tend to become insignificant as we move to 2015.
Michael J. Prather, Clare M. Flynn, Xin Zhu, Stephen D. Steenrod, Sarah A. Strode, Arlene M. Fiore, Gustavo Correa, Lee T. Murray, and Jean-Francois Lamarque
Atmos. Meas. Tech., 11, 2653–2668, https://doi.org/10.5194/amt-11-2653-2018, https://doi.org/10.5194/amt-11-2653-2018, 2018
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A new protocol for merging in situ atmospheric chemistry measurements with 3-D models is developed. This technique can identify the most reactive air parcels in terms of tropospheric production/loss of O3 & CH4. This approach highlights differences in 6 global chemistry models even with composition specified. Thus in situ measurements from, e.g., NASA's ATom mission can be used to develop a chemical climatology of, not only the key species, but also the rates of key reactions in each air parcel.
Robert Loughman, Pawan K. Bhartia, Zhong Chen, Philippe Xu, Ernest Nyaku, and Ghassan Taha
Atmos. Meas. Tech., 11, 2633–2651, https://doi.org/10.5194/amt-11-2633-2018, https://doi.org/10.5194/amt-11-2633-2018, 2018
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The Ozone Mapping and Profiler Suite (OMPS) Limb Profiler (LP) Version 1 algorithm retrieves aerosol extinction profiles at 675 nm by iteration, based on comparisons between the measured and calculated radiance profiles (assuming an aerosol size distribution). The most significant error source is uncertainty about the aerosol phase function. Horizontal variations in aerosol extinction may also limit the quality of the retrieved aerosol extinction profiles.
Pieternel F. Levelt, Joanna Joiner, Johanna Tamminen, J. Pepijn Veefkind, Pawan K. Bhartia, Deborah C. Stein Zweers, Bryan N. Duncan, David G. Streets, Henk Eskes, Ronald van der A, Chris McLinden, Vitali Fioletov, Simon Carn, Jos de Laat, Matthew DeLand, Sergey Marchenko, Richard McPeters, Jerald Ziemke, Dejian Fu, Xiong Liu, Kenneth Pickering, Arnoud Apituley, Gonzalo González Abad, Antti Arola, Folkert Boersma, Christopher Chan Miller, Kelly Chance, Martin de Graaf, Janne Hakkarainen, Seppo Hassinen, Iolanda Ialongo, Quintus Kleipool, Nickolay Krotkov, Can Li, Lok Lamsal, Paul Newman, Caroline Nowlan, Raid Suleiman, Lieuwe Gijsbert Tilstra, Omar Torres, Huiqun Wang, and Krzysztof Wargan
Atmos. Chem. Phys., 18, 5699–5745, https://doi.org/10.5194/acp-18-5699-2018, https://doi.org/10.5194/acp-18-5699-2018, 2018
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The aim of this paper is to highlight the many successes of the Ozone Monitoring Instrument (OMI) spanning more than 13 years. Data from OMI have been used in a wide range of applications. Due to its unprecedented spatial resolution, in combination with daily global coverage, OMI plays a unique role in measuring trace gases important for the ozone layer, air quality, and climate change. OMI data continue to be used for new research and applications.
Richard S. Stolarski, Anne R. Douglass, and Susan E. Strahan
Atmos. Chem. Phys., 18, 5691–5697, https://doi.org/10.5194/acp-18-5691-2018, https://doi.org/10.5194/acp-18-5691-2018, 2018
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Detecting trends in short data sets of stratospheric molecules is difficult because of variability due to dynamical fluctuations. We suggest that one way around this difficulty is using the measurements of one molecule to remove dynamical variability from the measurements of another molecule. We illustrate this using Aura MLS measurements of N2O to help us sort out issues in the determination of trends in HCl. This shows that HCl is decreasing throughout the middle stratosphere as expected.
Jungbin Mok, Nickolay A. Krotkov, Omar Torres, Hiren Jethva, Zhanqing Li, Jhoon Kim, Ja-Ho Koo, Sujung Go, Hitoshi Irie, Gordon Labow, Thomas F. Eck, Brent N. Holben, Jay Herman, Robert P. Loughman, Elena Spinei, Seoung Soo Lee, Pradeep Khatri, and Monica Campanelli
Atmos. Meas. Tech., 11, 2295–2311, https://doi.org/10.5194/amt-11-2295-2018, https://doi.org/10.5194/amt-11-2295-2018, 2018
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Measuring aerosol absorption from the shortest ultraviolet (UV) to the near-infrared (NIR) wavelengths is important for studies of climate, tropospheric photochemistry, human health, and agricultural productivity. We estimate the accuracy and demonstrate consistency of aerosol absorption retrievals from different instruments, after accounting for spectrally varying surface albedo and gaseous absorption.
Manuel López-Puertas, Maya García-Comas, Bernd Funke, Angela Gardini, Gabriele P. Stiller, Thomas von Clarmann, Norbert Glatthor, Alexandra Laeng, Martin Kaufmann, Viktoria F. Sofieva, Lucien Froidevaux, Kaley A. Walker, and Masato Shiotani
Atmos. Meas. Tech., 11, 2187–2212, https://doi.org/10.5194/amt-11-2187-2018, https://doi.org/10.5194/amt-11-2187-2018, 2018
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This paper describes the inversion of O3 data from MIPAS middle atmosphere spectra which requires non-LTE. The O3 dataset comprises from 20 to 100 km, has a pole-to-pole latitude coverage, day and nighttime, and span from 2005 until 2012. A validation of the data against other satellite measurements and an overall description of O3 is also presented. This is an important dataset for the community and describes the major characteristics of stratospheric and mesospheric O3.
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.
Chaim I. Garfinkel, Amit Gordon, Luke D. Oman, Feng Li, Sean Davis, and Steven Pawson
Atmos. Chem. Phys., 18, 4597–4615, https://doi.org/10.5194/acp-18-4597-2018, https://doi.org/10.5194/acp-18-4597-2018, 2018
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The impact of El Niño in the lower stratosphere is nonlinear in spring. While moderate El Niño events lead to cooling in this region,
strong El Niño events appear to lead to warming, and hence the water vapor response is nonlinear too. The net effect is that strong
El Nino events, such as in 1997/1998 and 2015/2016, lead to qualitatively different water vapor impacts as compared to moderate
El Nino events.
Mark Weber, Melanie Coldewey-Egbers, Vitali E. Fioletov, Stacey M. Frith, Jeannette D. Wild, John P. Burrows, Craig S. Long, and Diego Loyola
Atmos. Chem. Phys., 18, 2097–2117, https://doi.org/10.5194/acp-18-2097-2018, https://doi.org/10.5194/acp-18-2097-2018, 2018
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This paper commemorates the 30-year anniversary of the initial signing of the Montreal Protocol (MP) on substances that deplete the ozone layer. The MP is so far successful in reducing ozone-depleting substances, and total ozone decline was successfully stopped by the late 1990s. Total ozone levels have been mostly stable since then. In some regions, barely significant upward trends are observed that suggest an emergence into the expected ozone recovery phase.
William T. Ball, Justin Alsing, Daniel J. Mortlock, Johannes Staehelin, Joanna D. Haigh, Thomas Peter, Fiona Tummon, Rene Stübi, Andrea Stenke, John Anderson, Adam Bourassa, Sean M. Davis, Doug Degenstein, Stacey Frith, Lucien Froidevaux, Chris Roth, Viktoria Sofieva, Ray Wang, Jeannette Wild, Pengfei Yu, Jerald R. Ziemke, and Eugene V. Rozanov
Atmos. Chem. Phys., 18, 1379–1394, https://doi.org/10.5194/acp-18-1379-2018, https://doi.org/10.5194/acp-18-1379-2018, 2018
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Using a robust analysis, with artefact-corrected ozone data, we confirm upper stratospheric ozone is recovering following the Montreal Protocol, but that lower stratospheric ozone (50° S–50° N) has continued to decrease since 1998, and the ozone layer as a whole (60° S–60° N) may be lower today than in 1998. No change in total column ozone may be due to increasing tropospheric ozone. State-of-the-art models do not reproduce lower stratospheric ozone decreases.
Zhong Chen, Pawan K. Bhartia, Robert Loughman, and Peter Colarco
Atmos. Meas. Tech. Discuss., https://doi.org/10.5194/amt-2018-4, https://doi.org/10.5194/amt-2018-4, 2018
Revised manuscript has not been submitted
Olaf Morgenstern, Kane A. Stone, Robyn Schofield, Hideharu Akiyoshi, Yousuke Yamashita, Douglas E. Kinnison, Rolando R. Garcia, Kengo Sudo, David A. Plummer, John Scinocca, Luke D. Oman, Michael E. Manyin, Guang Zeng, Eugene Rozanov, Andrea Stenke, Laura E. Revell, Giovanni Pitari, Eva Mancini, Glauco Di Genova, Daniele Visioni, Sandip S. Dhomse, and Martyn P. Chipperfield
Atmos. Chem. Phys., 18, 1091–1114, https://doi.org/10.5194/acp-18-1091-2018, https://doi.org/10.5194/acp-18-1091-2018, 2018
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We assess how ozone as simulated by a group of chemistry–climate models responds to variations in man-made climate gases and ozone-depleting substances. We find some agreement, particularly in the middle and upper stratosphere, but also considerable disagreement elsewhere. Such disagreement affects the reliability of future ozone projections based on these models, and also constitutes a source of uncertainty in climate projections using prescribed ozone derived from these simulations.
Jay Herman, Liang Huang, Richard McPeters, Jerry Ziemke, Alexander Cede, and Karin Blank
Atmos. Meas. Tech., 11, 177–194, https://doi.org/10.5194/amt-11-177-2018, https://doi.org/10.5194/amt-11-177-2018, 2018
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We launched the DSCOVR spacecraft to an orbit located near the earth–sun gravitational plus centrifugal force balance point known as Lagrange 1. One of the earth-viewing instruments, EPIC, measures earth-reflected radiances in 10 wavelength channels ranging from 317.5 nm to 779.5 nm. We use the UV channels to retrieve O3 and scene reflectivity, and to derive the first measurement of erythemal flux (sunburn) from sunrise to sunset at the earth's surface.
Elizabeth C. Weatherhead, Jerald Harder, Eduardo A. Araujo-Pradere, Greg Bodeker, Jason M. English, Lawrence E. Flynn, Stacey M. Frith, Jeffrey K. Lazo, Peter Pilewskie, Mark Weber, and Thomas N. Woods
Atmos. Chem. Phys., 17, 15069–15093, https://doi.org/10.5194/acp-17-15069-2017, https://doi.org/10.5194/acp-17-15069-2017, 2017
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Satellite overlap is often carried out as a check on the stability of the data collected. We looked at how length of overlap influences how much information can be derived from the overlap period. Several results surprised us: the confidence we could have in the matchup of two records was independent of the offset, and understanding of the relative drift between the two satellite data sets improved significantly with 2–3 years of overlap. Sudden jumps could easily be confused with drift.
Stacey M. Frith, Richard S. Stolarski, Natalya A. Kramarova, and Richard D. McPeters
Atmos. Chem. Phys., 17, 14695–14707, https://doi.org/10.5194/acp-17-14695-2017, https://doi.org/10.5194/acp-17-14695-2017, 2017
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We have combined measurements from a series of SBUV instruments to create the longest continuous satellite-based profile ozone record from a single instrument type (1979–2016). We assess the consistency of the profile ozone measurements across instruments to assign an uncertainty to the merged record. Time-series analysis shows that upper-stratospheric ozone since 2001 is increasing, but the results are not yet statistically significant when the merged record uncertainties are included.
Jerald R. Ziemke, Sarah A. Strode, Anne R. Douglass, Joanna Joiner, Alexander Vasilkov, Luke D. Oman, Junhua Liu, Susan E. Strahan, Pawan K. Bhartia, and David P. Haffner
Atmos. Meas. Tech., 10, 4067–4078, https://doi.org/10.5194/amt-10-4067-2017, https://doi.org/10.5194/amt-10-4067-2017, 2017
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We combine satellite measurements of ozone and cloud properties from the Aura OMI and MLS instruments for 2004–2016 to measure ozone in the mid–upper levels of deep convective clouds. Our results ascribe upward injection of low boundary layer ozone (varying from low to high amounts) as a major driver of the measured concentrations of ozone in thick clouds. Our OMI/MLS generated ozone product is made available to the public for use in science applications.
Viktoria F. Sofieva, Erkki Kyrölä, Marko Laine, Johanna Tamminen, Doug Degenstein, Adam Bourassa, Chris Roth, Daniel Zawada, Mark Weber, Alexei Rozanov, Nabiz Rahpoe, Gabriele Stiller, Alexandra Laeng, Thomas von Clarmann, Kaley A. Walker, Patrick Sheese, Daan Hubert, Michel van Roozendael, Claus Zehner, Robert Damadeo, Joseph Zawodny, Natalya Kramarova, and Pawan K. Bhartia
Atmos. Chem. Phys., 17, 12533–12552, https://doi.org/10.5194/acp-17-12533-2017, https://doi.org/10.5194/acp-17-12533-2017, 2017
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We present a merged dataset of ozone profiles from several satellite instruments: SAGE II, GOMOS, SCIAMACHY, MIPAS, OSIRIS, ACE-FTS and OMPS. For merging, we used the latest versions of the original ozone datasets.
The merged SAGE–CCI–OMPS dataset is used for evaluating ozone trends in the stratosphere through multiple linear regression. Negative ozone trends in the upper stratosphere are observed before 1997 and positive trends are found after 1997.
Anne R. Douglass, Susan E. Strahan, Luke D. Oman, and Richard S. Stolarski
Atmos. Chem. Phys., 17, 12081–12096, https://doi.org/10.5194/acp-17-12081-2017, https://doi.org/10.5194/acp-17-12081-2017, 2017
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Data records from instruments on satellites and on the ground are compared with a simulation for 1980–2016 that is made using winds and temperatures that are derived from measurements. The simulation tracks the observations faithfully after about 2000, but there are systematic errors for earlier years. Scientists must take this into account when trying to detect and quantify changes in the stratospheric circulation that are caused by climate change.
Wolfgang Steinbrecht, Lucien Froidevaux, Ryan Fuller, Ray Wang, John Anderson, Chris Roth, Adam Bourassa, Doug Degenstein, Robert Damadeo, Joe Zawodny, Stacey Frith, Richard McPeters, Pawan Bhartia, Jeannette Wild, Craig Long, Sean Davis, Karen Rosenlof, Viktoria Sofieva, Kaley Walker, Nabiz Rahpoe, Alexei Rozanov, Mark Weber, Alexandra Laeng, Thomas von Clarmann, Gabriele Stiller, Natalya Kramarova, Sophie Godin-Beekmann, Thierry Leblanc, Richard Querel, Daan Swart, Ian Boyd, Klemens Hocke, Niklaus Kämpfer, Eliane Maillard Barras, Lorena Moreira, Gerald Nedoluha, Corinne Vigouroux, Thomas Blumenstock, Matthias Schneider, Omaira García, Nicholas Jones, Emmanuel Mahieu, Dan Smale, Michael Kotkamp, John Robinson, Irina Petropavlovskikh, Neil Harris, Birgit Hassler, Daan Hubert, and Fiona Tummon
Atmos. Chem. Phys., 17, 10675–10690, https://doi.org/10.5194/acp-17-10675-2017, https://doi.org/10.5194/acp-17-10675-2017, 2017
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Thanks to the 1987 Montreal Protocol and its amendments, ozone-depleting chlorine (and bromine) in the stratosphere has declined slowly since the late 1990s. Improved and extended long-term ozone profile observations from satellites and ground-based stations confirm that ozone is responding as expected and has increased by about 2 % per decade since 2000 in the upper stratosphere, around 40 km altitude. At lower altitudes, however, ozone has not changed significantly since 2000.
Katherine R. Travis, Daniel J. Jacob, Christoph A. Keller, Shi Kuang, Jintai Lin, Michael J. Newchurch, and Anne M. Thompson
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2017-596, https://doi.org/10.5194/acp-2017-596, 2017
Preprint retracted
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Models severely overestimate surface ozone in the Southeast US during summertime which has implications for the design of air quality regulations. We use a model (GEOS-Chem) to interpret ozone observations from a suite of observations taken during August–September 2013. The model is unbiased relative to observations below 1 km but is biased high at the surface. We attribute this bias to model representation error, an underestimate in low-cloud, and insufficient treatment of vertical mixing.
Michael J. Prather, Xin Zhu, Clare M. Flynn, Sarah A. Strode, Jose M. Rodriguez, Stephen D. Steenrod, Junhua Liu, Jean-Francois Lamarque, Arlene M. Fiore, Larry W. Horowitz, Jingqiu Mao, Lee T. Murray, Drew T. Shindell, and Steven C. Wofsy
Atmos. Chem. Phys., 17, 9081–9102, https://doi.org/10.5194/acp-17-9081-2017, https://doi.org/10.5194/acp-17-9081-2017, 2017
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We present a new approach for comparing atmospheric chemistry models with measurements based on what these models are used to do, i.e., calculate changes in ozone and methane, prime greenhouse gases. This method anticipates a new type of measurements from the NASA Atmospheric Tomography (ATom) mission. In comparing the mixture of species within air parcels, we focus on those responsible for key chemical changes and weight these parcels by their chemical reactivity.
Guanyu Huang, Xiong Liu, Kelly Chance, Kai Yang, Pawan K. Bhartia, Zhaonan Cai, Marc Allaart, Gérard Ancellet, Bertrand Calpini, Gerrie J. R. Coetzee, Emilio Cuevas-Agulló, Manuel Cupeiro, Hugo De Backer, Manvendra K. Dubey, Henry E. Fuelberg, Masatomo Fujiwara, Sophie Godin-Beekmann, Tristan J. Hall, Bryan Johnson, Everette Joseph, Rigel Kivi, Bogumil Kois, Ninong Komala, Gert König-Langlo, Giovanni Laneve, Thierry Leblanc, Marion Marchand, Kenneth R. Minschwaner, Gary Morris, Michael J. Newchurch, Shin-Ya Ogino, Nozomu Ohkawara, Ankie J. M. Piters, Françoise Posny, Richard Querel, Rinus Scheele, Frank J. Schmidlin, Russell C. Schnell, Otto Schrems, Henry Selkirk, Masato Shiotani, Pavla Skrivánková, René Stübi, Ghassan Taha, David W. Tarasick, Anne M. Thompson, Valérie Thouret, Matthew B. Tully, Roeland Van Malderen, Holger Vömel, Peter von der Gathen, Jacquelyn C. Witte, and Margarita Yela
Atmos. Meas. Tech., 10, 2455–2475, https://doi.org/10.5194/amt-10-2455-2017, https://doi.org/10.5194/amt-10-2455-2017, 2017
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It is essential to understand the data quality of +10-year OMI ozone product and impacts of the “row anomaly” (RA). We validate the OMI Ozone Profile (PROFOZ) product from Oct 2004 to Dec 2014 against ozonesonde observations globally. Generally, OMI has good agreement with ozonesondes. The spatiotemporal variation of retrieval performance suggests the need to improve OMI’s radiometric calibration especially during the post-RA period to maintain the long-term stability.
Olga V. Tweedy, Natalya A. Kramarova, Susan E. Strahan, Paul A. Newman, Lawrence Coy, William J. Randel, Mijeong Park, Darryn W. Waugh, and Stacey M. Frith
Atmos. Chem. Phys., 17, 6813–6823, https://doi.org/10.5194/acp-17-6813-2017, https://doi.org/10.5194/acp-17-6813-2017, 2017
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In this study we examined the impact of unprecedented disruption in the wind pattern (the quasi-biennial oscillation, or QBO) in the tropical stratosphere (16–48 km above the ground) on chemicals very important to the stratospheric climate such as ozone (O3). During the 2016 boreal summer, total O3 is lower in the extratropics than during previous QBO cycles due to lifting forced from the disruption. This decrease in O3 led to the increase in surface UV index by 8.5 % compared to the 36 yr mean.
V. M. Erik Schenkeveld, Glen Jaross, Sergey Marchenko, David Haffner, Quintus L. Kleipool, Nico C. Rozemeijer, J. Pepijn Veefkind, and Pieternel F. Levelt
Atmos. Meas. Tech., 10, 1957–1986, https://doi.org/10.5194/amt-10-1957-2017, https://doi.org/10.5194/amt-10-1957-2017, 2017
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The Ozone Monitoring Instrument (OMI) has been flying on NASA’s EOS Aura satellite since July 15, 2004. It has measured the concentration of trace gasses in the atmosphere, like ozone, NO2 and SO2. This article describes the trend in performance and calibration parameters of OMI during 12 years of flight. The degradation of the CCD detectors, solar diffusers, spectral calibration and row anomaly are shown. The instrument shows overall degradation that is better than expected.
Junhua Liu, Jose M. Rodriguez, Stephen D. Steenrod, Anne R. Douglass, Jennifer A. Logan, Mark A. Olsen, Krzysztof Wargan, and Jerald R. Ziemke
Atmos. Chem. Phys., 17, 3279–3299, https://doi.org/10.5194/acp-17-3279-2017, https://doi.org/10.5194/acp-17-3279-2017, 2017
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We quantify the relative contribution of processes controlling the interannual variability (IAV) of tropospheric ozone over the southern hemispheric tropospheric ozone maximum (SHTOM) with GMI chemistry transport model. We use various GMI tracer diagnostics, including a StratO3 tracer to quantify the stratospheric impact, and tagged CO tracers to track the emission sources. Our result shows that the stratospheric contribution is the most important factor driving the IAV of upper tropospheric O3.
Olaf Morgenstern, Michaela I. Hegglin, Eugene Rozanov, Fiona M. O'Connor, N. Luke Abraham, Hideharu Akiyoshi, Alexander T. Archibald, Slimane Bekki, Neal Butchart, Martyn P. Chipperfield, Makoto Deushi, Sandip S. Dhomse, Rolando R. Garcia, Steven C. Hardiman, Larry W. Horowitz, Patrick Jöckel, Beatrice Josse, Douglas Kinnison, Meiyun Lin, Eva Mancini, Michael E. Manyin, Marion Marchand, Virginie Marécal, Martine Michou, Luke D. Oman, Giovanni Pitari, David A. Plummer, Laura E. Revell, David Saint-Martin, Robyn Schofield, Andrea Stenke, Kane Stone, Kengo Sudo, Taichu Y. Tanaka, Simone Tilmes, Yousuke Yamashita, Kohei Yoshida, and Guang Zeng
Geosci. Model Dev., 10, 639–671, https://doi.org/10.5194/gmd-10-639-2017, https://doi.org/10.5194/gmd-10-639-2017, 2017
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We present a review of the make-up of 20 models participating in the Chemistry–Climate Model Initiative (CCMI). In comparison to earlier such activities, most of these models comprise a whole-atmosphere chemistry, and several of them include an interactive ocean module. This makes them suitable for studying the interactions of tropospheric air quality, stratospheric ozone, and climate. The paper lays the foundation for other studies using the CCMI simulations for scientific analysis.
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.
Chaim I. Garfinkel, Valentina Aquila, Darryn W. Waugh, and Luke D. Oman
Atmos. Chem. Phys., 17, 1313–1327, https://doi.org/10.5194/acp-17-1313-2017, https://doi.org/10.5194/acp-17-1313-2017, 2017
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Previous work has noted a discrepancy between models and observations in trends of the large-scale overturning circulation in the stratosphere. Here, we show that a model can simulate trends that are reminiscent of those observed, including space- and time-varying trends in different regions of the stratosphere. We therefore clarify that the statement that is often made that models simulate an accelerated circulation only applies over long time periods and is not true for the past 25 years.
Leslie Moy, Pawan K. Bhartia, Glen Jaross, Robert Loughman, Natalya Kramarova, Zhong Chen, Ghassan Taha, Grace Chen, and Philippe Xu
Atmos. Meas. Tech., 10, 167–178, https://doi.org/10.5194/amt-10-167-2017, https://doi.org/10.5194/amt-10-167-2017, 2017
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UV backscatter limb sounding sensors have difficulty determining altitude registration to the accuracy needed for long-term ozone monitoring. We describe two methods to achieve this by comparing radiance measurements to models. Wavelengths and altitudes chosen minimize errors from aerosol interference, calibration errors, and ozone assumptions. The techniques are inexpensive, more comprehensive than external sources of attitude information, and track drifts in our altitude to better than 100 m.
Juseon Bak, Xiong Liu, Jae H. Kim, Matthew T. Deland, and Kelly Chance
Atmos. Meas. Tech., 9, 4521–4531, https://doi.org/10.5194/amt-9-4521-2016, https://doi.org/10.5194/amt-9-4521-2016, 2016
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The main focus of this paper is improving an error of OMI nadir ozone profile retrievals due to the presence of polar mesospheric clouds (PMCs), consisting of small light-scattering particles at an altitude of 80–85 km. This error is shown to be systematic bias from ~ −2 at 2 hPa to ~ −20 % at 0.5 hPa and significantly correlated with brightness of PMCs. We reduce this interference of PMCs on ozone retrievals by including the PMC optical depth in the forward-model calculation and retrieval.
Raquel A. Silva, J. Jason West, Jean-François Lamarque, Drew T. Shindell, William J. Collins, Stig Dalsoren, Greg Faluvegi, Gerd Folberth, Larry W. Horowitz, Tatsuya Nagashima, Vaishali Naik, Steven T. Rumbold, Kengo Sudo, Toshihiko Takemura, Daniel Bergmann, Philip Cameron-Smith, Irene Cionni, Ruth M. Doherty, Veronika Eyring, Beatrice Josse, Ian A. MacKenzie, David Plummer, Mattia Righi, David S. Stevenson, Sarah Strode, Sophie Szopa, and Guang Zengast
Atmos. Chem. Phys., 16, 9847–9862, https://doi.org/10.5194/acp-16-9847-2016, https://doi.org/10.5194/acp-16-9847-2016, 2016
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Using ozone and PM2.5 concentrations from the ACCMIP ensemble of chemistry-climate models for the four Representative Concentration Pathway scenarios (RCPs), together with projections of future population and baseline mortality rates, we quantify the human premature mortality impacts of future ambient air pollution in 2030, 2050 and 2100, relative to 2000 concentrations. We also estimate the global mortality burden of ozone and PM2.5 in 2000 and each future period.
Pawan Gupta, Joanna Joiner, Alexander Vasilkov, and Pawan K. Bhartia
Atmos. Meas. Tech., 9, 2813–2826, https://doi.org/10.5194/amt-9-2813-2016, https://doi.org/10.5194/amt-9-2813-2016, 2016
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The A-train constellation of satellites provides a unique opportunity to analyze near-simultaneous data from several of these sensors. In this paper, retrievals of cloud/aerosols parameters and total column ozone (TCO) from the Aura Ozone Monitoring Instrument (OMI) have been used to develop a variety of neural networks that estimate TOA SWF globally over ocean and land using only OMI data as inputs. Application of our method to other ultraviolet sensors may provide unique estimates of TOA SWF.
Sarah A. Strode, Helen M. Worden, Megan Damon, Anne R. Douglass, Bryan N. Duncan, Louisa K. Emmons, Jean-Francois Lamarque, Michael Manyin, Luke D. Oman, Jose M. Rodriguez, Susan E. Strahan, and Simone Tilmes
Atmos. Chem. Phys., 16, 7285–7294, https://doi.org/10.5194/acp-16-7285-2016, https://doi.org/10.5194/acp-16-7285-2016, 2016
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We use global models to interpret trends in MOPITT observations of CO. Simulations with time-dependent emissions reproduce the observed trends over the eastern USA and Europe, suggesting that the emissions are reasonable for these regions. The simulations produce a positive trend over eastern China, contrary to the observed negative trend. This may indicate that the assumed emission trend over China is too positive. However, large variability in the overhead ozone column also contributes.
Zhong Chen, Matthew DeLand, and Pawan K. Bhartia
Atmos. Meas. Tech., 9, 1239–1246, https://doi.org/10.5194/amt-9-1239-2016, https://doi.org/10.5194/amt-9-1239-2016, 2016
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U. Jeong, J. Kim, C. Ahn, O. Torres, X. Liu, P. K. Bhartia, R. J. D. Spurr, D. Haffner, K. Chance, and B. N. Holben
Atmos. Chem. Phys., 16, 177–193, https://doi.org/10.5194/acp-16-177-2016, https://doi.org/10.5194/acp-16-177-2016, 2016
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An aerosol retrieval and error analysis algorithm using OMI measurements based on an optimal-estimation method was developed in this study. The aerosol retrievals were validated using the DRAGON campaign products. The estimated errors of the retrievals represented the actual biases between retrieval and AERONET measurements well. The retrievals, with their estimated uncertainties, are expected to be valuable for relevant studies, such as trace gas retrieval and data assimilation.
R. D. McPeters, S. Frith, and G. J. Labow
Atmos. Meas. Tech., 8, 4845–4850, https://doi.org/10.5194/amt-8-4845-2015, https://doi.org/10.5194/amt-8-4845-2015, 2015
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Comparisons show that ozone measured by OMI varied less than 1% relative to other NASA and European satellite instruments or relative to ground-based instruments. This means that OMI data can be used to reliably track global changes in ozone during the expected ozone recovery period and can be used to look for ozone signatures related to climate change.
S. A. Strode, B. N. Duncan, E. A. Yegorova, J. Kouatchou, J. R. Ziemke, and A. R. Douglass
Atmos. Chem. Phys., 15, 11789–11805, https://doi.org/10.5194/acp-15-11789-2015, https://doi.org/10.5194/acp-15-11789-2015, 2015
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A low bias in carbon monoxide (CO) at northern latitudes is a common feature of chemistry climate models. We find that increasing Northern Hemisphere (NH) CO emissions or reducing NH OH concentrations improves the agreement with CO surface observations, but reducing NH OH leads to a better comparison with MOPITT. Removing model biases in ozone and water vapor increases the simulated methane lifetime, but it does not give the 20% reduction in NH OH suggested by our analysis of the CO bias.
J. L. Schnell, M. J. Prather, B. Josse, V. Naik, L. W. Horowitz, P. Cameron-Smith, D. Bergmann, G. Zeng, D. A. Plummer, K. Sudo, T. Nagashima, D. T. Shindell, G. Faluvegi, and S. A. Strode
Atmos. Chem. Phys., 15, 10581–10596, https://doi.org/10.5194/acp-15-10581-2015, https://doi.org/10.5194/acp-15-10581-2015, 2015
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We test global chemistry--climate models in their ability to simulate present-day surface ozone. Models are tested against observed hourly ozone from 4217 stations in North America and Europe that are averaged over 1°x1° grid cells. Using novel metrics, we find most models match the shape but not the amplitude of regional summertime diurnal and annual cycles and match the pattern but not the magnitude of summer ozone enhancement. Most also match the observed distribution of extreme episode sizes
M. Coldewey-Egbers, D. G. Loyola, M. Koukouli, D. Balis, J.-C. Lambert, T. Verhoelst, J. Granville, M. van Roozendael, C. Lerot, R. Spurr, S. M. Frith, and C. Zehner
Atmos. Meas. Tech., 8, 3923–3940, https://doi.org/10.5194/amt-8-3923-2015, https://doi.org/10.5194/amt-8-3923-2015, 2015
J. Bak, X. Liu, J. H. Kim, M. T. Deland, and K. Chance
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acpd-15-25907-2015, https://doi.org/10.5194/acpd-15-25907-2015, 2015
Revised manuscript not accepted
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This work demonstrated the interference of tenuous PMCs on OMI ozone profile retrievals above 6hPa. The presence of PMCs leads to the systematic biases of -2% at 2hPa and -20% at 0.5hPa in OMI retrievals, which are significantly correlated with brightness of PMCs. We perform simultaneous retrievals of PMC optical depth with ozone using optimal estimation technique, to reduce the interference on ozone profile retrievals. As a result, the negative OMI biases are reduced to within ±10%.
N. R. P. Harris, B. Hassler, F. Tummon, G. E. Bodeker, D. Hubert, I. Petropavlovskikh, W. Steinbrecht, J. Anderson, P. K. Bhartia, C. D. Boone, A. Bourassa, S. M. Davis, D. Degenstein, A. Delcloo, S. M. Frith, L. Froidevaux, S. Godin-Beekmann, N. Jones, M. J. Kurylo, E. Kyrölä, M. Laine, S. T. Leblanc, J.-C. Lambert, B. Liley, E. Mahieu, A. Maycock, M. de Mazière, A. Parrish, R. Querel, K. H. Rosenlof, C. Roth, C. Sioris, J. Staehelin, R. S. Stolarski, R. Stübi, J. Tamminen, C. Vigouroux, K. A. Walker, H. J. Wang, J. Wild, and J. M. Zawodny
Atmos. Chem. Phys., 15, 9965–9982, https://doi.org/10.5194/acp-15-9965-2015, https://doi.org/10.5194/acp-15-9965-2015, 2015
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Trends in the vertical distribution of ozone are reported for new and recently revised data sets. The amount of ozone-depleting compounds in the stratosphere peaked in the second half of the 1990s. We examine the trends before and after that peak to see if any change in trend is discernible. The previously reported decreases are confirmed. Furthermore, the downward trend in upper stratospheric ozone has not continued. The possible significance of any increase is discussed in detail.
J. R. Ziemke, A. R. Douglass, L. D. Oman, S. E. Strahan, and B. N. Duncan
Atmos. Chem. Phys., 15, 8037–8049, https://doi.org/10.5194/acp-15-8037-2015, https://doi.org/10.5194/acp-15-8037-2015, 2015
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Aura OMI and MLS measurements are combined to produce daily maps of tropospheric ozone beginning October 2004. We show that El Niño Southern Oscillation (ENSO) related inter-annual change in tropospheric ozone in the tropics is small compared to combined intra-seasonal/Madden-Julian Oscillation (MJO) and shorter timescale variability. Outgoing Longwave Radiation indicates that deep convection is the primary driver of the observed ozone variability on all timescales.
L. K. Emmons, S. R. Arnold, S. A. Monks, V. Huijnen, S. Tilmes, K. S. Law, J. L. Thomas, J.-C. Raut, I. Bouarar, S. Turquety, Y. Long, B. Duncan, S. Steenrod, S. Strode, J. Flemming, J. Mao, J. Langner, A. M. Thompson, D. Tarasick, E. C. Apel, D. R. Blake, R. C. Cohen, J. Dibb, G. S. Diskin, A. Fried, S. R. Hall, L. G. Huey, A. J. Weinheimer, A. Wisthaler, T. Mikoviny, J. Nowak, J. Peischl, J. M. Roberts, T. Ryerson, C. Warneke, and D. Helmig
Atmos. Chem. Phys., 15, 6721–6744, https://doi.org/10.5194/acp-15-6721-2015, https://doi.org/10.5194/acp-15-6721-2015, 2015
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Eleven 3-D tropospheric chemistry models have been compared and evaluated with observations in the Arctic during the International Polar Year (IPY 2008). Large differences are seen among the models, particularly related to the model chemistry of volatile organic compounds (VOCs) and reactive nitrogen (NOx, PAN, HNO3) partitioning. Consistency among the models in the underestimation of CO, ethane and propane indicates the emission inventory is too low for these compounds.
R. Loughman, D. Flittner, E. Nyaku, and P. K. Bhartia
Atmos. Chem. Phys., 15, 3007–3020, https://doi.org/10.5194/acp-15-3007-2015, https://doi.org/10.5194/acp-15-3007-2015, 2015
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The Gauss--Seidel limb scattering (GSLS) radiative transfer model simulates the transfer of solar radiation through the atmosphere. Several recent changes have been added that improve the accuracy and flexibility of the GSLS radiance calculations. The single-scattered radiance errors have been reduced from 4% in earlier studies to 0.3%, while total radiance errors generally decline from 10% to 1-3%. In all cases, the tangent height dependence of the GSLS radiance error is greatly reduced.
F. Tummon, B. Hassler, N. R. P. Harris, J. Staehelin, W. Steinbrecht, J. Anderson, G. E. Bodeker, A. Bourassa, S. M. Davis, D. Degenstein, S. M. Frith, L. Froidevaux, E. Kyrölä, M. Laine, C. Long, A. A. Penckwitt, C. E. Sioris, K. H. Rosenlof, C. Roth, H.-J. Wang, and J. Wild
Atmos. Chem. Phys., 15, 3021–3043, https://doi.org/10.5194/acp-15-3021-2015, https://doi.org/10.5194/acp-15-3021-2015, 2015
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Understanding ozone trends in the vertical is vital in terms of assessing the success of the Montreal Protocol. This paper compares and analyses the long-term trends in stratospheric ozone from seven new merged satellite data sets. The data sets largely agree well with each other, particularly for the negative trends seen in the early period 1984-1997. For the 1998-2011 period there is less agreement, but a clear shift from negative to mostly positive trends.
J. Aschmann, J. P. Burrows, C. Gebhardt, A. Rozanov, R. Hommel, M. Weber, and A. M. Thompson
Atmos. Chem. Phys., 14, 12803–12814, https://doi.org/10.5194/acp-14-12803-2014, https://doi.org/10.5194/acp-14-12803-2014, 2014
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This study compares observations and simulation results of ozone in the lower tropical stratosphere. It shows that ozone in this region decreased from 1985 up to about 2002, which is consistent with an increase in tropical upwelling predicted by climate models. However, the decrease effectively stops after 2002, indicating that significant changes in tropical upwelling have occurred. The most important factor appears to be that the vertical ascent in the tropics is no longer accelerating.
A. Laeng, U. Grabowski, T. von Clarmann, G. Stiller, N. Glatthor, M. Höpfner, S. Kellmann, M. Kiefer, A. Linden, S. Lossow, V. Sofieva, I. Petropavlovskikh, D. Hubert, T. Bathgate, P. Bernath, C. D. Boone, C. Clerbaux, P. Coheur, R. Damadeo, D. Degenstein, S. Frith, L. Froidevaux, J. Gille, K. Hoppel, M. McHugh, Y. Kasai, J. Lumpe, N. Rahpoe, G. Toon, T. Sano, M. Suzuki, J. Tamminen, J. Urban, K. Walker, M. Weber, and J. Zawodny
Atmos. Meas. Tech., 7, 3971–3987, https://doi.org/10.5194/amt-7-3971-2014, https://doi.org/10.5194/amt-7-3971-2014, 2014
A. M. Thompson, N. V. Balashov, J. C. Witte, J. G. R. Coetzee, V. Thouret, and F. Posny
Atmos. Chem. Phys., 14, 9855–9869, https://doi.org/10.5194/acp-14-9855-2014, https://doi.org/10.5194/acp-14-9855-2014, 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
E. W. Chiou, P. K. Bhartia, R. D. McPeters, D. G. Loyola, M. Coldewey-Egbers, V. E. Fioletov, M. Van Roozendael, R. Spurr, C. Lerot, and S. M. Frith
Atmos. Meas. Tech., 7, 1681–1692, https://doi.org/10.5194/amt-7-1681-2014, https://doi.org/10.5194/amt-7-1681-2014, 2014
B. Hassler, I. Petropavlovskikh, J. Staehelin, T. August, P. K. Bhartia, C. Clerbaux, D. Degenstein, M. De Mazière, B. M. Dinelli, A. Dudhia, G. Dufour, S. M. Frith, L. Froidevaux, S. Godin-Beekmann, J. Granville, N. R. P. Harris, K. Hoppel, D. Hubert, Y. Kasai, M. J. Kurylo, E. Kyrölä, J.-C. Lambert, P. F. Levelt, C. T. McElroy, R. D. McPeters, R. Munro, H. Nakajima, A. Parrish, P. Raspollini, E. E. Remsberg, K. H. Rosenlof, A. Rozanov, T. Sano, Y. Sasano, M. Shiotani, H. G. J. Smit, G. Stiller, J. Tamminen, D. W. Tarasick, J. Urban, R. J. van der A, J. P. Veefkind, C. Vigouroux, T. von Clarmann, C. von Savigny, K. A. Walker, M. Weber, J. Wild, and J. M. Zawodny
Atmos. Meas. Tech., 7, 1395–1427, https://doi.org/10.5194/amt-7-1395-2014, https://doi.org/10.5194/amt-7-1395-2014, 2014
M. Chin, T. Diehl, Q. Tan, J. M. Prospero, R. A. Kahn, L. A. Remer, H. Yu, A. M. Sayer, H. Bian, I. V. Geogdzhayev, B. N. Holben, S. G. Howell, B. J. Huebert, N. C. Hsu, D. Kim, T. L. Kucsera, R. C. Levy, M. I. Mishchenko, X. Pan, P. K. Quinn, G. L. Schuster, D. G. Streets, S. A. Strode, O. Torres, and X.-P. Zhao
Atmos. Chem. Phys., 14, 3657–3690, https://doi.org/10.5194/acp-14-3657-2014, https://doi.org/10.5194/acp-14-3657-2014, 2014
N. A. Kramarova, E. R. Nash, P. A. Newman, P. K. Bhartia, R. D. McPeters, D. F. Rault, C. J. Seftor, P. Q. Xu, and G. J. Labow
Atmos. Chem. Phys., 14, 2353–2361, https://doi.org/10.5194/acp-14-2353-2014, https://doi.org/10.5194/acp-14-2353-2014, 2014
L. K. Huang, M. T. DeLand, S. L. Taylor, and L. E. Flynn
Atmos. Meas. Tech., 7, 267–278, https://doi.org/10.5194/amt-7-267-2014, https://doi.org/10.5194/amt-7-267-2014, 2014
C. Gebhardt, A. Rozanov, R. Hommel, M. Weber, H. Bovensmann, J. P. Burrows, D. Degenstein, L. Froidevaux, and A. M. Thompson
Atmos. Chem. Phys., 14, 831–846, https://doi.org/10.5194/acp-14-831-2014, https://doi.org/10.5194/acp-14-831-2014, 2014
R. M. Stauffer, G. A. Morris, A. M. Thompson, E. Joseph, G. J. R. Coetzee, and N. R. Nalli
Atmos. Meas. Tech., 7, 65–79, https://doi.org/10.5194/amt-7-65-2014, https://doi.org/10.5194/amt-7-65-2014, 2014
M. M. Hurwitz, L. D. Oman, P. A. Newman, and I.-S. Song
Atmos. Chem. Phys., 13, 12187–12197, https://doi.org/10.5194/acp-13-12187-2013, https://doi.org/10.5194/acp-13-12187-2013, 2013
E. J. Bucsela, N. A. Krotkov, E. A. Celarier, L. N. Lamsal, W. H. Swartz, P. K. Bhartia, K. F. Boersma, J. P. Veefkind, J. F. Gleason, and K. E. Pickering
Atmos. Meas. Tech., 6, 2607–2626, https://doi.org/10.5194/amt-6-2607-2013, https://doi.org/10.5194/amt-6-2607-2013, 2013
P. K. Bhartia, R. D. McPeters, L. E. Flynn, S. Taylor, N. A. Kramarova, S. Frith, B. Fisher, and M. DeLand
Atmos. Meas. Tech., 6, 2533–2548, https://doi.org/10.5194/amt-6-2533-2013, https://doi.org/10.5194/amt-6-2533-2013, 2013
J. Herman, M. T. DeLand, L.-K. Huang, G. Labow, D. Larko, S. A. Lloyd, J. Mao, W. Qin, and C. Weaver
Atmos. Chem. Phys., 13, 8505–8524, https://doi.org/10.5194/acp-13-8505-2013, https://doi.org/10.5194/acp-13-8505-2013, 2013
N. A. Kramarova, P. K. Bhartia, S. M. Frith, R. D. McPeters, and R. S. Stolarski
Atmos. Meas. Tech., 6, 2089–2099, https://doi.org/10.5194/amt-6-2089-2013, https://doi.org/10.5194/amt-6-2089-2013, 2013
J.-F. Lamarque, F. Dentener, J. McConnell, C.-U. Ro, M. Shaw, R. Vet, D. Bergmann, P. Cameron-Smith, S. Dalsoren, R. Doherty, G. Faluvegi, S. J. Ghan, B. Josse, Y. H. Lee, I. A. MacKenzie, D. Plummer, D. T. Shindell, R. B. Skeie, D. S. Stevenson, S. Strode, G. Zeng, M. Curran, D. Dahl-Jensen, S. Das, D. Fritzsche, and M. Nolan
Atmos. Chem. Phys., 13, 7997–8018, https://doi.org/10.5194/acp-13-7997-2013, https://doi.org/10.5194/acp-13-7997-2013, 2013
N. A. Kramarova, S. M. Frith, P. K. Bhartia, R. D. McPeters, S. L. Taylor, B. L. Fisher, G. J. Labow, and M. T. DeLand
Atmos. Chem. Phys., 13, 6887–6905, https://doi.org/10.5194/acp-13-6887-2013, https://doi.org/10.5194/acp-13-6887-2013, 2013
V. Naik, A. Voulgarakis, A. M. Fiore, L. W. Horowitz, J.-F. Lamarque, M. Lin, M. J. Prather, P. J. Young, D. Bergmann, P. J. Cameron-Smith, I. Cionni, W. J. Collins, S. B. Dalsøren, R. Doherty, V. Eyring, G. Faluvegi, G. A. Folberth, B. Josse, Y. H. Lee, I. A. MacKenzie, T. Nagashima, T. P. C. van Noije, D. A. Plummer, M. Righi, S. T. Rumbold, R. Skeie, D. T. Shindell, D. S. Stevenson, S. Strode, K. Sudo, S. Szopa, and G. Zeng
Atmos. Chem. Phys., 13, 5277–5298, https://doi.org/10.5194/acp-13-5277-2013, https://doi.org/10.5194/acp-13-5277-2013, 2013
K. W. Bowman, D. T. Shindell, H. M. Worden, J.F. Lamarque, P. J. Young, D. S. Stevenson, Z. Qu, M. de la Torre, D. Bergmann, P. J. Cameron-Smith, W. J. Collins, R. Doherty, S. B. Dalsøren, G. Faluvegi, G. Folberth, L. W. Horowitz, B. M. Josse, Y. H. Lee, I. A. MacKenzie, G. Myhre, T. Nagashima, V. Naik, D. A. Plummer, S. T. Rumbold, R. B. Skeie, S. A. Strode, K. Sudo, S. Szopa, A. Voulgarakis, G. Zeng, S. S. Kulawik, A. M. Aghedo, and J. R. Worden
Atmos. Chem. Phys., 13, 4057–4072, https://doi.org/10.5194/acp-13-4057-2013, https://doi.org/10.5194/acp-13-4057-2013, 2013
D. S. Stevenson, P. J. Young, V. Naik, J.-F. Lamarque, D. T. Shindell, A. Voulgarakis, R. B. Skeie, S. B. Dalsoren, G. Myhre, T. K. Berntsen, G. A. Folberth, S. T. Rumbold, W. J. Collins, I. A. MacKenzie, R. M. Doherty, G. Zeng, T. P. C. van Noije, A. Strunk, D. Bergmann, P. Cameron-Smith, D. A. Plummer, S. A. Strode, L. Horowitz, Y. H. Lee, S. Szopa, K. Sudo, T. Nagashima, B. Josse, I. Cionni, M. Righi, V. Eyring, A. Conley, K. W. Bowman, O. Wild, and A. Archibald
Atmos. Chem. Phys., 13, 3063–3085, https://doi.org/10.5194/acp-13-3063-2013, https://doi.org/10.5194/acp-13-3063-2013, 2013
A. Voulgarakis, V. Naik, J.-F. Lamarque, D. T. Shindell, P. J. Young, M. J. Prather, O. Wild, R. D. Field, D. Bergmann, P. Cameron-Smith, I. Cionni, W. J. Collins, S. B. Dalsøren, R. M. Doherty, V. Eyring, G. Faluvegi, G. A. Folberth, L. W. Horowitz, B. Josse, I. A. MacKenzie, T. Nagashima, D. A. Plummer, M. Righi, S. T. Rumbold, D. S. Stevenson, S. A. Strode, K. Sudo, S. Szopa, and G. Zeng
Atmos. Chem. Phys., 13, 2563–2587, https://doi.org/10.5194/acp-13-2563-2013, https://doi.org/10.5194/acp-13-2563-2013, 2013
P. J. Young, A. T. Archibald, K. W. Bowman, J.-F. Lamarque, V. Naik, D. S. Stevenson, S. Tilmes, A. Voulgarakis, O. Wild, D. Bergmann, P. Cameron-Smith, I. Cionni, W. J. Collins, S. B. Dalsøren, R. M. Doherty, V. Eyring, G. Faluvegi, L. W. Horowitz, B. Josse, Y. H. Lee, I. A. MacKenzie, T. Nagashima, D. A. Plummer, M. Righi, S. T. Rumbold, R. B. Skeie, D. T. Shindell, S. A. Strode, K. Sudo, S. Szopa, and G. Zeng
Atmos. Chem. Phys., 13, 2063–2090, https://doi.org/10.5194/acp-13-2063-2013, https://doi.org/10.5194/acp-13-2063-2013, 2013
J.-F. Lamarque, D. T. Shindell, B. Josse, P. J. Young, I. Cionni, V. Eyring, D. Bergmann, P. Cameron-Smith, W. J. Collins, R. Doherty, S. Dalsoren, G. Faluvegi, G. Folberth, S. J. Ghan, L. W. Horowitz, Y. H. Lee, I. A. MacKenzie, T. Nagashima, V. Naik, D. Plummer, M. Righi, S. T. Rumbold, M. Schulz, R. B. Skeie, D. S. Stevenson, S. Strode, K. Sudo, S. Szopa, A. Voulgarakis, and G. Zeng
Geosci. Model Dev., 6, 179–206, https://doi.org/10.5194/gmd-6-179-2013, https://doi.org/10.5194/gmd-6-179-2013, 2013
G. A. Morris, G. Labow, H. Akimoto, M. Takigawa, M. Fujiwara, F. Hasebe, J. Hirokawa, and T. Koide
Atmos. Chem. Phys., 13, 1243–1260, https://doi.org/10.5194/acp-13-1243-2013, https://doi.org/10.5194/acp-13-1243-2013, 2013
Related subject area
Subject: Gases | Research Activity: Remote Sensing | Altitude Range: Troposphere | Science Focus: Physics (physical properties and processes)
Quantifying large methane emissions from the Nord Stream pipeline gas leak of September 2022 using IASI satellite observations and inverse modelling
Automated detection of regions with persistently enhanced methane concentrations using Sentinel-5 Precursor satellite data
Biomass burning CO emissions: exploring insights through TROPOMI-derived emissions and emission coefficients
Measurement report: Combined use of MAX-DOAS and AERONET ground-based measurements in Montevideo, Uruguay, for the detection of distant biomass burning
Development of high spatial resolution annual emission inventory of greenhouse gases from open straw burning in Northeast China from 2001 to 2020
Quantifying CH4 emissions from coal mine aggregation areas in Shanxi, China, using TROPOMI observations and the wind-assigned anomaly method
Identifying episodic carbon monoxide emission events in the MOPITT measurement dataset
Quantifying effects of long-range transport of NO2 over Delhi using back trajectories and satellite data
Measurement report: Ammonia in Paris derived from ground-based open-path and satellite observations
Anthropogenic CO2 emission estimates in the Tokyo metropolitan area from ground-based CO2 column observations
Characterizing the tropospheric water vapor spatial variation and trend using 2007–2018 COSMIC radio occultation and ECMWF reanalysis data
Detecting nitrogen oxide emissions in Qatar and quantifying emission factors of gas-fired power plants – a 4-year study
Identifying and accounting for the Coriolis effect in satellite NO2 observations and emission estimates
Characterisations of Europe's integrated water vapour and assessments of atmospheric reanalyses using more than 2 decades of ground-based GPS
Ground-level gaseous pollutants (NO2, SO2, and CO) in China: daily seamless mapping and spatiotemporal variations
NH3 spatiotemporal variability over Paris, Mexico City, and Toronto, and its link to PM2.5 during pollution events
Multi-axis differential optical absorption spectroscopy (MAX-DOAS) observations of formaldehyde and nitrogen dioxide at three sites in Asia and comparison with the global chemistry transport model CHASER
Quantifying CH4 emissions in hard coal mines from TROPOMI and IASI observations using the wind-assigned anomaly method
Estimation of surface ammonia concentrations and emissions in China from the polar-orbiting Infrared Atmospheric Sounding Interferometer and the FY-4A Geostationary Interferometric Infrared Sounder
Interannual variability in the Australian carbon cycle over 2015–2019, based on assimilation of Orbiting Carbon Observatory-2 (OCO-2) satellite data
Source and variability of formaldehyde (HCHO) at northern high latitudes: an integrated satellite, aircraft, and model study
Volcanic SO2 layer height by TROPOMI/S5P: evaluation against IASI/MetOp and CALIOP/CALIPSO observations
Spaceborne tropospheric nitrogen dioxide (NO2) observations from 2005–2020 over the Yangtze River Delta (YRD), China: variabilities, implications, and drivers
Novel assessment of numerical forecasting model relative humidity with satellite probabilistic estimates
Influence of springtime atmospheric circulation types on the distribution of air pollutants in the Arctic
Technical note: Evaluation of profile retrievals of aerosols and trace gases for MAX-DOAS measurements under different aerosol scenarios based on radiative transfer simulations
Diurnal evolution of total column and surface atmospheric ammonia in the megacity of Paris, France, during an intense springtime pollution episode
The reduction in C2H6 from 2015 to 2020 over Hefei, eastern China, points to air quality improvement in China
Mapping the drivers of formaldehyde (HCHO) variability from 2015 to 2019 over eastern China: insights from Fourier transform infrared observation and GEOS-Chem model simulation
The impact of Los Angeles Basin pollution and stratospheric intrusions on the surrounding San Gabriel Mountains as seen by surface measurements, lidar, and numerical models
Sudden changes in nitrogen dioxide emissions over Greece due to lockdown after the outbreak of COVID-19
Monitoring CO emissions of the metropolis Mexico City using TROPOMI CO observations
Pollution trace gas distributions and their transport in the Asian monsoon upper troposphere and lowermost stratosphere during the StratoClim campaign 2017
Spatial distribution of enhanced BrO and its relation to meteorological parameters in Arctic and Antarctic sea ice regions
Trends of atmospheric water vapour in Switzerland from ground-based radiometry, FTIR and GNSS data
A Raman lidar tropospheric water vapour climatology and height-resolved trend analysis over Payerne, Switzerland
The potential of Orbiting Carbon Observatory-2 data to reduce the uncertainties in CO2 surface fluxes over Australia using a variational assimilation scheme
Observing carbon dioxide emissions over China's cities and industrial areas with the Orbiting Carbon Observatory-2
Observational evidence of moistening the lowermost stratosphere via isentropic mixing across the subtropical jet
Fourier transform infrared time series of tropospheric HCN in eastern China: seasonality, interannual variability, and source attribution
NH3 emissions from large point sources derived from CrIS and IASI satellite observations
Diurnal cycle of short-term fluctuations of integrated water vapour above Switzerland
Retrieval of total column and surface NO2 from Pandora zenith-sky measurements
MAX-DOAS measurements of tropospheric NO2 and HCHO in Nanjing and a comparison to ozone monitoring instrument observations
Consistency and representativeness of integrated water vapour from ground-based GPS observations and ERA-Interim reanalysis
Towards monitoring localized CO2 emissions from space: co-located regional CO2 and NO2 enhancements observed by the OCO-2 and S5P satellites
Variability of bulk water vapor content in the marine cloudy boundary layers from microwave and near-infrared imagery
Trends and trend reversal detection in 2 decades of tropospheric NO2 satellite observations
Satellite-derived sulfur dioxide (SO2) emissions from the 2014–2015 Holuhraun eruption (Iceland)
Emissions of methane in Europe inferred by total column measurements
Chris Wilson, Brian J. Kerridge, Richard Siddans, David P. Moore, Lucy J. Ventress, Emily Dowd, Wuhu Feng, Martyn P. Chipperfield, and John J. Remedios
Atmos. Chem. Phys., 24, 10639–10653, https://doi.org/10.5194/acp-24-10639-2024, https://doi.org/10.5194/acp-24-10639-2024, 2024
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The leaks from the Nord Stream gas pipelines in September 2022 released a large amount of methane (CH4) into the atmosphere. We provide observational data from a satellite instrument that shows a large CH4 plume over the North Sea off the coast of Scandinavia. We use this together with atmospheric models to quantify the CH4 leaked into the atmosphere from the pipelines. We find that 219–427 Gg CH4 was emitted, making this the largest individual fossil-fuel-related CH4 leak on record.
Steffen Vanselow, Oliver Schneising, Michael Buchwitz, Maximilian Reuter, Heinrich Bovensmann, Hartmut Boesch, and John P. Burrows
Atmos. Chem. Phys., 24, 10441–10473, https://doi.org/10.5194/acp-24-10441-2024, https://doi.org/10.5194/acp-24-10441-2024, 2024
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We developed an algorithm to automatically detect persistent methane source regions, to quantify their emissions and to determine their source types, by analyzing TROPOMI data from 2018–2021. The over 200 globally detected natural and anthropogenic source regions include small-scale point sources such as individual coal mines and larger-scale source regions such as wetlands and large oil and gas fields.
Debora Griffin, Jack Chen, Kerry Anderson, Paul Makar, Chris A. McLinden, Enrico Dammers, and Andre Fogal
Atmos. Chem. Phys., 24, 10159–10186, https://doi.org/10.5194/acp-24-10159-2024, https://doi.org/10.5194/acp-24-10159-2024, 2024
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Satellite-derived CO emissions provide new insights into the understanding of global CO emission rates from wildfires. We use TROPOMI satellite data to create a global inventory database of wildfire CO emissions. These satellite-derived wildfire emissions are used for the evaluation and improvement of existing fire emission inventories and to examine how the wildfire CO emissions have changed over the past 2 decades.
Matías Osorio, Alejandro Agesta, Tim Bösch, Nicolás Casaballe, Andreas Richter, Leonardo M. A. Alvarado, and Erna Frins
Atmos. Chem. Phys., 24, 7447–7465, https://doi.org/10.5194/acp-24-7447-2024, https://doi.org/10.5194/acp-24-7447-2024, 2024
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This study concerns the detection and quantification of long-transport emissions of a biomass burning event, which represents a major source of air pollutants, due to the release of large amounts of aerosols and chemical species into the atmosphere. The quantification was done using ground-based observations (which play an important role in assessing the abundance of trace gases and aerosols) over Montevideo (Uruguay) and using satellite observations.
Zihan Song, Leiming Zhang, Chongguo Tian, Qiang Fu, Zhenxing Shen, Renjian Zhang, Dong Liu, and Song Cui
EGUsphere, https://doi.org/10.5194/egusphere-2024-980, https://doi.org/10.5194/egusphere-2024-980, 2024
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1. A novel concept integrating crop cycle information into fire spots extraction was proposed. 2. Spatiotemporal variations of open straw burning in Northeast China were revealed. 3. Open straw burning in Northeast China emitted a total of 221 Tg of CO2-eq during 2001–2020. 4. The policy of banning straw burning effectively reduced greenhouse gases emissions.
Qiansi Tu, Frank Hase, Kai Qin, Jason Blake Cohen, Farahnaz Khosrawi, Xinrui Zou, Matthias Schneider, and Fan Lu
Atmos. Chem. Phys., 24, 4875–4894, https://doi.org/10.5194/acp-24-4875-2024, https://doi.org/10.5194/acp-24-4875-2024, 2024
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Four-year satellite observations of XCH4 are used to derive CH4 emissions in three regions of China’s coal-rich Shanxi province. The wind-assigned anomalies for two opposite wind directions are calculated, and the estimated emission rates are comparable to the current bottom-up inventory but lower than the CAMS and EDGAR inventories. This research enhances the understanding of emissions in Shanxi and supports climate mitigation strategies by validating emission inventories.
Paul S. Jeffery, James R. Drummond, Jiansheng Zou, and Kaley A. Walker
Atmos. Chem. Phys., 24, 4253–4263, https://doi.org/10.5194/acp-24-4253-2024, https://doi.org/10.5194/acp-24-4253-2024, 2024
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The MOPITT instrument has been monitoring carbon monoxide (CO) since March 2000. This dataset has been used for many applications; however, episodic emission events, which release large amounts of CO into the atmosphere, are a major source of uncertainty. This study presents a method for identifying these events by determining measurements that are unlikely to have typically arisen. The distribution and frequency of these flagged measurements in the MOPITT dataset are presented and discussed.
Ailish M. Graham, Richard J. Pope, Martyn P. Chipperfield, Sandip S. Dhomse, Matilda Pimlott, Wuhu Feng, Vikas Singh, Ying Chen, Oliver Wild, Ranjeet Sokhi, and Gufran Beig
Atmos. Chem. Phys., 24, 789–806, https://doi.org/10.5194/acp-24-789-2024, https://doi.org/10.5194/acp-24-789-2024, 2024
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Our paper uses novel satellite datasets and high-resolution emissions datasets alongside a back-trajectory model to investigate the balance of local and external sources influencing NOx air pollution changes in Delhi. We find in the post-monsoon season that NOx from local and non-local transport emissions contributes most to poor air quality in Delhi. Therefore, air quality mitigation strategies in Delhi and surrounding regions are used to control this issue.
Camille Viatte, Nadir Guendouz, Clarisse Dufaux, Arjan Hensen, Daan Swart, Martin Van Damme, Lieven Clarisse, Pierre Coheur, and Cathy Clerbaux
Atmos. Chem. Phys., 23, 15253–15267, https://doi.org/10.5194/acp-23-15253-2023, https://doi.org/10.5194/acp-23-15253-2023, 2023
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Ammonia (NH3) is an important air pollutant which, as a precursor of fine particulate matter, raises public health concerns. Models have difficulty predicting events of pollution associated with NH3 since ground-based observations of this gas are still relatively sparse and difficult to implement. We present the first relatively long (2.5 years) and continuous record of hourly NH3 concentrations in Paris to determine its temporal variabilities at different scales to unravel emission sources.
Hirofumi Ohyama, Matthias M. Frey, Isamu Morino, Kei Shiomi, Masahide Nishihashi, Tatsuya Miyauchi, Hiroko Yamada, Makoto Saito, Masanobu Wakasa, Thomas Blumenstock, and Frank Hase
Atmos. Chem. Phys., 23, 15097–15119, https://doi.org/10.5194/acp-23-15097-2023, https://doi.org/10.5194/acp-23-15097-2023, 2023
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We conducted a field campaign for CO2 column measurements in the Tokyo metropolitan area with three ground-based Fourier transform spectrometers. The model simulations using prior CO2 fluxes were generally in good agreement with the observations. We developed an urban-scale inversion system in which spatially resolved CO2 fluxes and a scaling factor of large point source emissions were estimated. The posterior total CO2 emissions agreed with emission inventories within the posterior uncertainty.
Xi Shao, Shu-Peng Ho, Xin Jing, Xinjia Zhou, Yong Chen, Tung-Chang Liu, Bin Zhang, and Jun Dong
Atmos. Chem. Phys., 23, 14187–14218, https://doi.org/10.5194/acp-23-14187-2023, https://doi.org/10.5194/acp-23-14187-2023, 2023
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Atmospheric water vapor plays an essential role in the global energy balance, hydrological cycle, and climate system. This paper characterizes and compares the global, latitudinal, and regional variabilities of COSMIC and ERA5 water vapor distribution, as well as the seasonality and long-term trends at selected pressure levels from 2007 to 2018. Evaluation of spatiotemporal variabilities of atmospheric water vapor ensures the qualities of COSMIC and reanalysis water vapor for climate studies.
Anthony Rey-Pommier, Frédéric Chevallier, Philippe Ciais, Jonilda Kushta, Theodoros Christoudias, I. Safak Bayram, and Jean Sciare
Atmos. Chem. Phys., 23, 13565–13583, https://doi.org/10.5194/acp-23-13565-2023, https://doi.org/10.5194/acp-23-13565-2023, 2023
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We use four years (2019–2022) of TROPOMI NO2 data to map NOx emissions in Qatar. We estimate average monthly emissions for the country and industrial facilities and derive an emission factor for the power sector. Monthly emissions have a weekly cycle reflecting the social norms in Qatar and an annual cycle consistent with the electricity production by gas-fired power plants. Their mean value is lower than the NOx emissions in global inventories but similar to the emissions reported for 2007.
Daniel A. Potts, Roger Timmis, Emma J. S. Ferranti, and Joshua D. Vande Hey
Atmos. Chem. Phys., 23, 4577–4593, https://doi.org/10.5194/acp-23-4577-2023, https://doi.org/10.5194/acp-23-4577-2023, 2023
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With the launch of the TROPOspheric Monitoring Instrument (TROPOMI) in 2017, it is now possible to observe pollutants emitted from individual industrial facilities on a daily basis around the globe. By using observations of nitrogen dioxide (NO2) from 16 different industrial sites, we show how the Coriolis effect influences the trajectory of these emission plumes as well as how the additional curvature can lead to a substantial underestimation of the calculated emissions.
Peng Yuan, Roeland Van Malderen, Xungang Yin, Hannes Vogelmann, Weiping Jiang, Joseph Awange, Bernhard Heck, and Hansjörg Kutterer
Atmos. Chem. Phys., 23, 3517–3541, https://doi.org/10.5194/acp-23-3517-2023, https://doi.org/10.5194/acp-23-3517-2023, 2023
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Water vapour plays an important role in various weather and climate processes. However, due to its large spatiotemporal variability, its high-accuracy quantification remains a challenge. In this study, 20+ years of GPS-derived integrated water vapour (IWV) retrievals in Europe were obtained. They were then used to characterise the temporal features of Europe's IWV and assess six atmospheric reanalyses. Results show that ERA5 outperforms the other reanalyses at most temporal scales.
Jing Wei, Zhanqing Li, Jun Wang, Can Li, Pawan Gupta, and Maureen Cribb
Atmos. Chem. Phys., 23, 1511–1532, https://doi.org/10.5194/acp-23-1511-2023, https://doi.org/10.5194/acp-23-1511-2023, 2023
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This study estimated the daily seamless 10 km ambient gaseous pollutants (NO2, SO2, and CO) across China using machine learning with extensive input variables measured on monitors, satellites, and models. Our dataset yields a high data quality via cross-validation at varying spatiotemporal scales and outperforms most previous related studies, making it most helpful to future (especially short-term) air pollution and environmental health-related studies.
Camille Viatte, Rimal Abeed, Shoma Yamanouchi, William C. Porter, Sarah Safieddine, Martin Van Damme, Lieven Clarisse, Beatriz Herrera, Michel Grutter, Pierre-Francois Coheur, Kimberly Strong, and Cathy Clerbaux
Atmos. Chem. Phys., 22, 12907–12922, https://doi.org/10.5194/acp-22-12907-2022, https://doi.org/10.5194/acp-22-12907-2022, 2022
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Large cities can experience high levels of fine particulate matter (PM2.5) pollution linked to ammonia (NH3) mainly emitted from agricultural activities. Using a combination of PM2.5 and NH3 measurements from in situ instruments, satellite infrared spectrometers, and atmospheric model simulations, we have demonstrated the role of NH3 and meteorological conditions on pollution events occurring over Paris, Toronto, and Mexico City.
Hossain Mohammed Syedul Hoque, Kengo Sudo, Hitoshi Irie, Alessandro Damiani, Manish Naja, and Al Mashroor Fatmi
Atmos. Chem. Phys., 22, 12559–12589, https://doi.org/10.5194/acp-22-12559-2022, https://doi.org/10.5194/acp-22-12559-2022, 2022
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Nitrogen dioxide (NO2) and formaldehyde (HCHO) are essential trace graces regulating tropospheric ozone chemistry. These trace constituents are measured using an optical passive remote sensing technique. In addition, NO2 and HCHO are simulated with a computer model and evaluated against the observations. Such evaluations are essential to assess model uncertainties and improve their predictability. The results yielded good agreement between the two datasets with some discrepancies.
Qiansi Tu, Matthias Schneider, Frank Hase, Farahnaz Khosrawi, Benjamin Ertl, Jaroslaw Necki, Darko Dubravica, Christopher J. Diekmann, Thomas Blumenstock, and Dianjun Fang
Atmos. Chem. Phys., 22, 9747–9765, https://doi.org/10.5194/acp-22-9747-2022, https://doi.org/10.5194/acp-22-9747-2022, 2022
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Three-year satellite observations and high-resolution model forecast of XCH4 are used to derive CH4 emissions in the USCB region, Poland – a region of intense coal mining activities. The wind-assigned anomalies for two opposite wind directions are calculated and the estimated emission rates are very close to the inventories and in reasonable agreement with the previous studies. Our method is quite robust and can serve as a simple method to estimate CH4 or CO2 emissions for other regions.
Pu Liu, Jia Ding, Lei Liu, Wen Xu, and Xuejun Liu
Atmos. Chem. Phys., 22, 9099–9110, https://doi.org/10.5194/acp-22-9099-2022, https://doi.org/10.5194/acp-22-9099-2022, 2022
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Ammonia (NH3) is the important alkaline gas and the key component of fine particulate matter. We used satellite-based observations to analyze the changes in hourly NH3 concentrations and estimated surface NH3 concentrations and NH3 emissions in China. This study shows enormous potential for using satellite data to estimate surface NH3 concentrations and NH3 emissions and provides an important reference for understanding NH3 variation in China.
Yohanna Villalobos, Peter J. Rayner, Jeremy D. Silver, Steven Thomas, Vanessa Haverd, Jürgen Knauer, Zoë M. Loh, Nicholas M. Deutscher, David W. T. Griffith, and David F. Pollard
Atmos. Chem. Phys., 22, 8897–8934, https://doi.org/10.5194/acp-22-8897-2022, https://doi.org/10.5194/acp-22-8897-2022, 2022
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We study the interannual variability in Australian carbon fluxes for 2015–2019 derived from OCO-2 satellite data. Our results suggest that Australia's semi-arid ecosystems are highly responsive to variations in climate drivers such as rainfall and temperature. We found that high rainfall and low temperatures recorded in 2016 led to an anomalous carbon sink over savanna and sparsely vegetated regions, while unprecedented dry and hot weather in 2019 led to anomalous carbon release.
Tianlang Zhao, Jingqiu Mao, William R. Simpson, Isabelle De Smedt, Lei Zhu, Thomas F. Hanisco, Glenn M. Wolfe, Jason M. St. Clair, Gonzalo González Abad, Caroline R. Nowlan, Barbara Barletta, Simone Meinardi, Donald R. Blake, Eric C. Apel, and Rebecca S. Hornbrook
Atmos. Chem. Phys., 22, 7163–7178, https://doi.org/10.5194/acp-22-7163-2022, https://doi.org/10.5194/acp-22-7163-2022, 2022
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Monitoring formaldehyde (HCHO) can help us understand Arctic vegetation change. Here, we compare satellite data and model and show that Alaska summertime HCHO is largely dominated by a background from methane oxidation during mild wildfire years and is dominated by wildfire (largely from direct emission of fire) during strong fire years. Consequently, it is challenging to use satellite HCHO to study vegetation change in the Arctic region.
Maria-Elissavet Koukouli, Konstantinos Michailidis, Pascal Hedelt, Isabelle A. Taylor, Antje Inness, Lieven Clarisse, Dimitris Balis, Dmitry Efremenko, Diego Loyola, Roy G. Grainger, and Christian Retscher
Atmos. Chem. Phys., 22, 5665–5683, https://doi.org/10.5194/acp-22-5665-2022, https://doi.org/10.5194/acp-22-5665-2022, 2022
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Volcanic eruptions eject large amounts of ash and trace gases into the atmosphere. The use of space-borne instruments enables the global monitoring of volcanic SO2 emissions in an economical and risk-free manner. The main aim of this paper is to present its extensive verification, accomplished within the ESA S5P+I: SO2LH project, over major recent volcanic eruptions, against collocated space-borne measurements, as well as assess its impact on the forecasts provided by CAMS.
Hao Yin, Youwen Sun, Justus Notholt, Mathias Palm, and Cheng Liu
Atmos. Chem. Phys., 22, 4167–4185, https://doi.org/10.5194/acp-22-4167-2022, https://doi.org/10.5194/acp-22-4167-2022, 2022
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In this study, we quantity the long-term variabilities and the underlying drivers of NO2 from 2005 to 2020 over the Yangtze River Delta (YRD), one of the most densely populated and highly industrialized city clusters in China. We reveal the significant effect of the Action Plan on the Prevention and Control of Air Pollution since 2013 adopted by the Chinese government to reduce NOx pollution. Our study can improve the understanding of pollution control measures on a regional scale.
Chloé Radice, Hélène Brogniez, Pierre-Emmanuel Kirstetter, and Philippe Chambon
Atmos. Chem. Phys., 22, 3811–3825, https://doi.org/10.5194/acp-22-3811-2022, https://doi.org/10.5194/acp-22-3811-2022, 2022
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A novel probabilistic approach is proposed to evaluate relative humidity (RH) profiles simulated by an atmospheric model with respect to satellite-based RH defined from probability distributions. It improves upon deterministic comparisons by enhancing the information content to enable a finer assessment of each model–observation discrepancy, highlighting significant departures within a deterministic confidence range. Geographical and vertical distributions of the model biases are discussed.
Manu Anna Thomas, Abhay Devasthale, and Tiina Nygård
Atmos. Chem. Phys., 21, 16593–16608, https://doi.org/10.5194/acp-21-16593-2021, https://doi.org/10.5194/acp-21-16593-2021, 2021
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The impact of transported pollutants and their spatial distribution in the Arctic are governed by the local atmospheric circulation or weather states. Therefore, we investigated eight different atmospheric circulation types observed during the spring season in the Arctic. Using satellite and reanalysis datasets, this study provides a comprehensive assessment of the typical circulation patterns that can lead to enhanced or reduced pollution concentrations in the different sectors of the Arctic.
Xin Tian, Yang Wang, Steffen Beirle, Pinhua Xie, Thomas Wagner, Jin Xu, Ang Li, Steffen Dörner, Bo Ren, and Xiaomei Li
Atmos. Chem. Phys., 21, 12867–12894, https://doi.org/10.5194/acp-21-12867-2021, https://doi.org/10.5194/acp-21-12867-2021, 2021
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The performances of two MAX-DOAS inversion algorithms were evaluated for various aerosol pollution scenarios. One inversion algorithm is based on optimal estimation; the other uses a parameterized approach. In this analysis, three types of profile shapes for aerosols and NO2 were considered: exponential, Boltzmann, and Gaussian. The evaluation results can effectively guide the application of the two inversion algorithms in the actual atmosphere and improve the accuracy of the actual inversion.
Rebecca D. Kutzner, Juan Cuesta, Pascale Chelin, Jean-Eudes Petit, Mokhtar Ray, Xavier Landsheere, Benoît Tournadre, Jean-Charles Dupont, Amandine Rosso, Frank Hase, Johannes Orphal, and Matthias Beekmann
Atmos. Chem. Phys., 21, 12091–12111, https://doi.org/10.5194/acp-21-12091-2021, https://doi.org/10.5194/acp-21-12091-2021, 2021
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Our work investigates the diurnal evolution of atmospheric ammonia concentrations during a major pollution event. It analyses it in regard of both chemical (gas–particle conversion) and physical (vertical mixing, meteorology) processes in the atmosphere. These mechanisms are key for understanding the evolution of the physicochemical state of the atmosphere; therefore, it clearly fits into the scope of Atmospheric Chemistry and Physics.
Youwen Sun, Hao Yin, Cheng Liu, Emmanuel Mahieu, Justus Notholt, Yao Té, Xiao Lu, Mathias Palm, Wei Wang, Changgong Shan, Qihou Hu, Min Qin, Yuan Tian, and Bo Zheng
Atmos. Chem. Phys., 21, 11759–11779, https://doi.org/10.5194/acp-21-11759-2021, https://doi.org/10.5194/acp-21-11759-2021, 2021
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The variability, sources, and transport of ethane (C2H6) over eastern China from 2015 to 2020 were studied using ground-based Fourier transform infrared (FTIR) spectroscopy and GEOS-Chem simulations. C2H6 variability is driven by both meteorological and emission factors. The reduction in C2H6 in recent years over eastern China points to air quality improvement in China.
Youwen Sun, Hao Yin, Cheng Liu, Lin Zhang, Yuan Cheng, Mathias Palm, Justus Notholt, Xiao Lu, Corinne Vigouroux, Bo Zheng, Wei Wang, Nicholas Jones, Changong Shan, Min Qin, Yuan Tian, Qihou Hu, Fanhao Meng, and Jianguo Liu
Atmos. Chem. Phys., 21, 6365–6387, https://doi.org/10.5194/acp-21-6365-2021, https://doi.org/10.5194/acp-21-6365-2021, 2021
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This study mapped the drivers of HCHO variability from 2015 to 2019 over eastern China. Hydroxyl (OH) radical production rates from HCHO photolysis were evaluated. The relative contributions of emitted and photochemical sources to the observed HCHO abundance were analyzed. Contributions of various emission sources and geographical regions to the observed HCHO summertime enhancements were determined.
Fernando Chouza, Thierry Leblanc, Mark Brewer, Patrick Wang, Sabino Piazzolla, Gabriele Pfister, Rajesh Kumar, Carl Drews, Simone Tilmes, Louisa Emmons, and Matthew Johnson
Atmos. Chem. Phys., 21, 6129–6153, https://doi.org/10.5194/acp-21-6129-2021, https://doi.org/10.5194/acp-21-6129-2021, 2021
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The tropospheric ozone lidar at the JPL Table Mountain Facility (TMF) was used to investigate the impact of Los Angeles (LA) Basin pollution transport and stratospheric intrusions in the planetary boundary layer on the San Gabriel Mountains. The results of this study indicate a dominant role of the LA Basin pollution on days when high ozone levels were observed at TMF (March–October period).
Maria-Elissavet Koukouli, Ioanna Skoulidou, Andreas Karavias, Isaak Parcharidis, Dimitris Balis, Astrid Manders, Arjo Segers, Henk Eskes, and Jos van Geffen
Atmos. Chem. Phys., 21, 1759–1774, https://doi.org/10.5194/acp-21-1759-2021, https://doi.org/10.5194/acp-21-1759-2021, 2021
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In recent years, satellite observations have contributed to monitoring air quality. During the first COVID-19 lockdown, lower levels of nitrogen dioxide were observed over Greece by S5P/TROPOMI for March and April 2020 (than the preceding year) due to decreased transport emissions. Taking meteorology into account, using LOTOS-EUROS CTM simulations, the resulting decline due to the lockdown was estimated to range between 0 % and −37 % for the five largest Greek cities, with an average of ~ −10 %.
Tobias Borsdorff, Agustín García Reynoso, Gilberto Maldonado, Bertha Mar-Morales, Wolfgang Stremme, Michel Grutter, and Jochen Landgraf
Atmos. Chem. Phys., 20, 15761–15774, https://doi.org/10.5194/acp-20-15761-2020, https://doi.org/10.5194/acp-20-15761-2020, 2020
Sören Johansson, Michael Höpfner, Oliver Kirner, Ingo Wohltmann, Silvia Bucci, Bernard Legras, Felix Friedl-Vallon, Norbert Glatthor, Erik Kretschmer, Jörn Ungermann, and Gerald Wetzel
Atmos. Chem. Phys., 20, 14695–14715, https://doi.org/10.5194/acp-20-14695-2020, https://doi.org/10.5194/acp-20-14695-2020, 2020
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We present high-resolution measurements of pollutant trace gases (PAN, C2H2, and HCOOH) in the Asian monsoon UTLS from the airborne limb imager GLORIA during StratoClim 2017. Enhancements are observed up to 16 km altitude, and PAN and C2H2 even up to 18 km. Two atmospheric models, CAMS and EMAC, reproduce the pollutant's large-scale structures but not finer structures. Convection is investigated using backward trajectories of the models ATLAS and TRACZILLA with advanced detection of convection.
Sora Seo, Andreas Richter, Anne-Marlene Blechschmidt, Ilias Bougoudis, and John Philip Burrows
Atmos. Chem. Phys., 20, 12285–12312, https://doi.org/10.5194/acp-20-12285-2020, https://doi.org/10.5194/acp-20-12285-2020, 2020
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In this study, we present spatial distributions of occurrence frequency of enhanced total BrO column and various meteorological parameters affecting it in the Arctic and Antarctic sea ice regions by using 10 years of GOME-2 measurements and meteorological model data. Statistical analysis using the long-term dataset shows clear differences in the meteorological conditions between the mean field and the situation of enhanced total BrO columns in both polar sea ice regions.
Leonie Bernet, Elmar Brockmann, Thomas von Clarmann, Niklaus Kämpfer, Emmanuel Mahieu, Christian Mätzler, Gunter Stober, and Klemens Hocke
Atmos. Chem. Phys., 20, 11223–11244, https://doi.org/10.5194/acp-20-11223-2020, https://doi.org/10.5194/acp-20-11223-2020, 2020
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With global warming, water vapour increases in the atmosphere. Water vapour is an important gas because it is a natural greenhouse gas and affects the formation of clouds, rain and snow. How much water vapour increases can vary in different regions of the world. To verify if it increases as expected on a regional scale, we analysed water vapour measurements in Switzerland. We found that water vapour generally increases as expected from temperature changes, except in winter.
Shannon Hicks-Jalali, Robert J. Sica, Giovanni Martucci, Eliane Maillard Barras, Jordan Voirin, and Alexander Haefele
Atmos. Chem. Phys., 20, 9619–9640, https://doi.org/10.5194/acp-20-9619-2020, https://doi.org/10.5194/acp-20-9619-2020, 2020
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We have calculated an 11.5-year water vapour climatology using the Raman Lidar for Meteorological Observations (RALMO), located in Payerne, Switzerland. The climatology shows that the highest water vapour concentrations are in the summer months and the lowest in the winter months. We present for the first time height-resolved water vapour trends, which show that water vapour increases specific humidity by between 5 % and 15 % per decade depending on the altitude.
Yohanna Villalobos, Peter Rayner, Steven Thomas, and Jeremy Silver
Atmos. Chem. Phys., 20, 8473–8500, https://doi.org/10.5194/acp-20-8473-2020, https://doi.org/10.5194/acp-20-8473-2020, 2020
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Estimated carbon fluxes for Australia are subject to considerable uncertainty. We ran simulation experiments over Australia to determine how much these uncertainties can be constrained using satellite data. We found that the satellite data has the potential to reduce these uncertainties up to 80 % across the whole continent. For 1 month, this percentage corresponds to 0.51 Pg C y-1 for Australia. This method could lead to significantly more accurate estimates of Australia's carbon budget.
Bo Zheng, Frédéric Chevallier, Philippe Ciais, Grégoire Broquet, Yilong Wang, Jinghui Lian, and Yuanhong Zhao
Atmos. Chem. Phys., 20, 8501–8510, https://doi.org/10.5194/acp-20-8501-2020, https://doi.org/10.5194/acp-20-8501-2020, 2020
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The Paris Climate Agreement requires all parties to report CO2 emissions regularly. Given the self-reporting nature of this system, it is critical to evaluate the emission reports with independent observation systems. Here we present the direct observations of city CO2 plumes from space and the quantification of CO2 emissions from these observations over the largest emitter country China. The emissions from 46 hot-spot regions representing 13 % of China's total emissions can be well constrained.
Jeffery Langille, Adam Bourassa, Laura L. Pan, Daniel Letros, Brian Solheim, Daniel Zawada, and Doug Degenstein
Atmos. Chem. Phys., 20, 5477–5486, https://doi.org/10.5194/acp-20-5477-2020, https://doi.org/10.5194/acp-20-5477-2020, 2020
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Water vapour (WV) is a highly variable and extremely important trace gas in Earth’s atmosphere. Due to its radiative and chemical properties, it is coupled to the climate in an extremely complex manner. This is especially true in the lowermost stratosphere (LMS). Despite its importance, the physical processes that control mixing and the distribution of WV in the LMS are poorly understood. This study provides observational evidence of moistening the LMS via mixing across the subtropical jet.
Youwen Sun, Cheng Liu, Lin Zhang, Mathias Palm, Justus Notholt, Hao Yin, Corinne Vigouroux, Erik Lutsch, Wei Wang, Changong Shan, Thomas Blumenstock, Tomoo Nagahama, Isamu Morino, Emmanuel Mahieu, Kimberly Strong, Bavo Langerock, Martine De Mazière, Qihou Hu, Huifang Zhang, Christof Petri, and Jianguo Liu
Atmos. Chem. Phys., 20, 5437–5456, https://doi.org/10.5194/acp-20-5437-2020, https://doi.org/10.5194/acp-20-5437-2020, 2020
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We present multiyear time series of ground-based Fourier-transform infrared spectroscopy measurements of HCN in densely populated eastern China. The seasonality and interannual variability of tropospheric HCN columns were investigated. The potential sources that drive the observed HCN seasonality and interannual variability were determined using a GEOS-Chem tagged CO simulation, global fire maps, and potential source contribution function values calculated using HYSPLIT back trajectories.
Enrico Dammers, Chris A. McLinden, Debora Griffin, Mark W. Shephard, Shelley Van Der Graaf, Erik Lutsch, Martijn Schaap, Yonatan Gainairu-Matz, Vitali Fioletov, Martin Van Damme, Simon Whitburn, Lieven Clarisse, Karen Cady-Pereira, Cathy Clerbaux, Pierre Francois Coheur, and Jan Willem Erisman
Atmos. Chem. Phys., 19, 12261–12293, https://doi.org/10.5194/acp-19-12261-2019, https://doi.org/10.5194/acp-19-12261-2019, 2019
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Ammonia is an essential molecule in the environment, but at its current levels it is unsustainable. However, the emissions are highly uncertain. We explore the use of satellites to estimate the ammonia lifetime and emissions around point sources to help improve the budget. The same method applied to different satellite instruments shows consistent results. Comparison to the emission inventories shows that those are underestimating emissions of point sources by on average a factor of 2.5.
Klemens Hocke, Leonie Bernet, Jonas Hagen, Axel Murk, Matthias Renker, and Christian Mätzler
Atmos. Chem. Phys., 19, 12083–12090, https://doi.org/10.5194/acp-19-12083-2019, https://doi.org/10.5194/acp-19-12083-2019, 2019
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The Tropospheric Water Radiometer (TROWARA) observed an enhanced intensity of short-term integrated water vapour (IWV) fluctuations during daytime in summer. These IWV fluctuations are possibly related to latent heat flux and thermal convective activity in the lower troposphere. The observed climatology and spectra of IWV fluctuations might be useful for modelling studies of water vapour convection in the atmospheric boundary layer at mid latitudes.
Xiaoyi Zhao, Debora Griffin, Vitali Fioletov, Chris McLinden, Jonathan Davies, Akira Ogyu, Sum Chi Lee, Alexandru Lupu, Michael D. Moran, Alexander Cede, Martin Tiefengraber, and Moritz Müller
Atmos. Chem. Phys., 19, 10619–10642, https://doi.org/10.5194/acp-19-10619-2019, https://doi.org/10.5194/acp-19-10619-2019, 2019
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New nitrogen dioxide (NO2) retrieval algorithms are developed for Pandora zenith-sky measurements. A column-to-surface conversion look-up table was produced for the Pandora instruments; therefore, quick and practical Pandora-based surface NO2 concentration data can be obtained for air quality monitoring purposes. It is demonstrated that the surface NO2 concentration is controlled not only by the planetary boundary layer height but also by both boundary layer dynamics and photochemistry.
Ka Lok Chan, Zhuoru Wang, Aijun Ding, Klaus-Peter Heue, Yicheng Shen, Jing Wang, Feng Zhang, Yining Shi, Nan Hao, and Mark Wenig
Atmos. Chem. Phys., 19, 10051–10071, https://doi.org/10.5194/acp-19-10051-2019, https://doi.org/10.5194/acp-19-10051-2019, 2019
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The paper presents long-term observations of atmospheric nitrogen dioxide (NO2) and formaldehyde (HCHO) in Nanjing using a MAX-DOAS instrument. The measurements were performed from April 2013 to February 2017. The MAX-DOAS measurements of NO2 and HCHO are used to validate OMI satellite observations and to investigate the influences of region transport of air pollutants on the air quality in Nanjing.
Olivier Bock and Ana C. Parracho
Atmos. Chem. Phys., 19, 9453–9468, https://doi.org/10.5194/acp-19-9453-2019, https://doi.org/10.5194/acp-19-9453-2019, 2019
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We examine the consistency of global IWV data from ERA-Interim reanalysis and 16 years of GPS observations. Representativeness differences are found to be a dominant error source, with a strong dependence on geographic, topographic, and climatic features, which explain both average and extreme differences. A methodology for reducing the representativeness errors and detecting the extreme, outlying, cases is discussed.
Maximilian Reuter, Michael Buchwitz, Oliver Schneising, Sven Krautwurst, Christopher W. O'Dell, Andreas Richter, Heinrich Bovensmann, and John P. Burrows
Atmos. Chem. Phys., 19, 9371–9383, https://doi.org/10.5194/acp-19-9371-2019, https://doi.org/10.5194/acp-19-9371-2019, 2019
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The quantification of anthropogenic emissions with current CO2 satellite sensors is difficult, but NO2 is co-emitted, making it a suitable tracer of recently emitted CO2. We analyze enhancements of CO2 and NO2 observed by OCO-2 and S5P and estimate the CO2 plume cross-sectional fluxes that we compare with emission databases. Our results demonstrate the usefulness of simultaneous satellite observations of CO2 and NO2 as envisaged for the European Copernicus anthropogenic CO2 monitoring mission
Luis F. Millán, Matthew D. Lebsock, and Joao Teixeira
Atmos. Chem. Phys., 19, 8491–8502, https://doi.org/10.5194/acp-19-8491-2019, https://doi.org/10.5194/acp-19-8491-2019, 2019
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The synergy of the collocated Advanced Microwave Scanning Radiometer (AMSR) and the Moderate Resolution Imaging Spectroradiometer (MODIS) provides daily global estimates of marine boundary layer water vapor. AMSR provides the total column water vapor, while MODIS provides the water vapor above the cloud layers. The difference between the two gives the vapor between the surface and the cloud top, which may be interpreted as the boundary layer water vapor.
Aristeidis K. Georgoulias, Ronald J. van der A, Piet Stammes, K. Folkert Boersma, and Henk J. Eskes
Atmos. Chem. Phys., 19, 6269–6294, https://doi.org/10.5194/acp-19-6269-2019, https://doi.org/10.5194/acp-19-6269-2019, 2019
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In this paper, a ∼21-year self-consistent global dataset from four different satellite sensors is compiled for the first time to study the long-term tropospheric NO2 patterns and trends. A novel method capable of detecting the year when a reversal of trends happened shows that tropospheric NO2 concentrations switched from positive to negative trends and vice versa over several regions around the globe during the last 2 decades.
Elisa Carboni, Tamsin A. Mather, Anja Schmidt, Roy G. Grainger, Melissa A. Pfeffer, Iolanda Ialongo, and Nicolas Theys
Atmos. Chem. Phys., 19, 4851–4862, https://doi.org/10.5194/acp-19-4851-2019, https://doi.org/10.5194/acp-19-4851-2019, 2019
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The 2014–2015 Holuhraun eruption was the largest in Iceland for 200 years, emitting huge quantities of gas into the troposphere, at times overwhelming European anthropogenic emissions. Infrared Atmospheric sounding Interferometer data are used to derive the first time series of daily sulfur dioxide mass and vertical distribution over the eruption period. A scheme is used to estimate sulfur dioxide fluxes, the total erupted mass, and how long the sulfur dioxide remains in the atmosphere.
Debra Wunch, Dylan B. A. Jones, Geoffrey C. Toon, Nicholas M. Deutscher, Frank Hase, Justus Notholt, Ralf Sussmann, Thorsten Warneke, Jeroen Kuenen, Hugo Denier van der Gon, Jenny A. Fisher, and Joannes D. Maasakkers
Atmos. Chem. Phys., 19, 3963–3980, https://doi.org/10.5194/acp-19-3963-2019, https://doi.org/10.5194/acp-19-3963-2019, 2019
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We used five atmospheric observatories in Europe measuring total column dry-air mole fractions of methane and carbon monoxide to infer methane emissions in the area between the observatories. We find that the methane emissions are overestimated by the state-of-the-art inventories, and that this is likely due, at least in part, to the inventory disaggregation. We find that there is significant uncertainty in the carbon monoxide inventories that requires further investigation.
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