Articles | Volume 15, issue 20
https://doi.org/10.5194/acp-15-11789-2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
https://doi.org/10.5194/acp-15-11789-2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Research article
| 
23 Oct 2015
Research article |
| 23 Oct 2015
Implications of carbon monoxide bias for methane lifetime and atmospheric composition in chemistry climate models
GESTAR, Universities Space Research Association, Columbia, MD, USA
NASA Goddard Space Flight Center, Greenbelt, MD, USA
B. N. Duncan
NASA Goddard Space Flight Center, Greenbelt, MD, USA
E. A. Yegorova
NASA Goddard Space Flight Center, Greenbelt, MD, USA
Earth System Science Interdisciplinary Center, College Park, MD, USA
now at: Nuclear Regulatory Commission, Rockville, MD, USA
J. Kouatchou
NASA Goddard Space Flight Center, Greenbelt, MD, USA
Science Systems and Applications Inc., Lanham, MD, USA
J. R. Ziemke
NASA Goddard Space Flight Center, Greenbelt, MD, USA
GESTAR, Morgan State University, Baltimore, MD, USA
A. R. Douglass
NASA Goddard Space Flight Center, Greenbelt, MD, USA
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This introduction to the special issue "Achievements and perspectives of the Network for the Detection of Atmospheric Composition Change after 35 years of operation” provides an overview of important research findings achieved under the NDACC objectives. The future of NDACC is discussed in the light of the evolution of the scientific questions, evolving collaborations with partners and Cooperating Networks, and the current landscape of gaps in satellite and ground-based observations.
Caterina Mogno, Peter R. Colarco, Allison B. Collow, Sampa Das, Sarah A. Strode, Vanessa Valenti, Michael E. Manyin, Qing Liang, Luke Oman, Stephen D. Steenrod, and K. Emma Knowland
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We investigated a climate model's ability to simulate atmospheric aerosols focusing on the relationship between mass and optical properties, by comparing predictions with observations. Our analysis revealed that model errors in aerosol scattering primarily stem from inaccurate particle mass concentrations and relative humidity, rather than flawed optical property assumptions in the model. These findings point out improvements for enhancing the accuracy for aerosols representation in our model.
Huisheng Bian, Sarah Strode, Mian Chin, Fan Li, Andrea Molad, Peter R. Colarco, and Hongbin Yu
EGUsphere, https://doi.org/10.5194/egusphere-2025-4501, https://doi.org/10.5194/egusphere-2025-4501, 2025
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We study the North Pacific westerly jet (NPWJ) using four reanalysis datasets and eight CMIP6 models. Our results show that between 1980 and 2019, the NPWJ core oscillates seasonally between north and south, weakening and shifting northward in summer and autumn. Single-forcing simulations further reveal aerosol forcing as the main driver. Incorporating interacting chemistry and time-varying ozone radiative forcing into Earth system models is crucial for simulating long-term atmospheric dynamics.
Bryan N. Duncan, Daniel C. Anderson, Arlene M. Fiore, Joanna Joiner, Nickolay A. Krotkov, Can Li, Dylan B. Millet, Julie M. Nicely, Luke D. Oman, Jason M. St. Clair, Joshua D. Shutter, Amir H. Souri, Sarah A. Strode, Brad Weir, Glenn M. Wolfe, Helen M. Worden, and Qindan Zhu
Atmos. Chem. Phys., 24, 13001–13023, https://doi.org/10.5194/acp-24-13001-2024, https://doi.org/10.5194/acp-24-13001-2024, 2024
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Trace gases emitted to or formed within the atmosphere may be chemically or physically removed from the atmosphere. One trace gas, the hydroxyl radical (OH), is responsible for initiating the chemical removal of many trace gases, including some greenhouse gases. Despite its importance, scientists have not been able to adequately measure OH. In this opinion piece, we discuss promising new methods to indirectly constrain OH using satellite data of trace gases that control the abundance of OH.
Yasin Elshorbany, Jerald R. Ziemke, Sarah Strode, Hervé Petetin, Kazuyuki Miyazaki, Isabelle De Smedt, Kenneth Pickering, Rodrigo J. Seguel, Helen Worden, Tamara Emmerichs, Domenico Taraborrelli, Maria Cazorla, Suvarna Fadnavis, Rebecca R. Buchholz, Benjamin Gaubert, Néstor Y. Rojas, Thiago Nogueira, Thérèse Salameh, and Min Huang
Atmos. Chem. Phys., 24, 12225–12257, https://doi.org/10.5194/acp-24-12225-2024, https://doi.org/10.5194/acp-24-12225-2024, 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 CO, as well as ozonesonde data and model simulations.
Pinchas Nürnberg, Sarah A. Strode, and Ralf Sussmann
Atmos. Chem. Phys., 24, 10001–10012, https://doi.org/10.5194/acp-24-10001-2024, https://doi.org/10.5194/acp-24-10001-2024, 2024
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We created a set of scaling factors describing the diurnal increase in stratospheric nitrogen oxides above Zugspitze, Germany. We used these factors to validate recently published model simulation data. On the one hand, this validation enables the use of the validated data to better understand the stratospheric photochemistry. On the other hand, it can improve satellite validation, which has implications for the understanding of urban smog events and other pollution events in the troposphere.
Amir H. Souri, Bryan N. Duncan, Sarah A. Strode, Daniel C. Anderson, Michael E. Manyin, Junhua Liu, Luke D. Oman, Zhen Zhang, and Brad Weir
Atmos. Chem. Phys., 24, 8677–8701, https://doi.org/10.5194/acp-24-8677-2024, https://doi.org/10.5194/acp-24-8677-2024, 2024
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We explore a new method of using the wealth of information obtained from satellite observations of Aura OMI NO2, HCHO, and MERRA-2 reanalysis in NASA’s GEOS model equipped with an efficient tropospheric OH (TOH) estimator to enhance the representation of TOH spatial distribution and its long-term trends. This new framework helps us pinpoint regional inaccuracies in TOH and differentiate between established prior knowledge and newly acquired information from satellites on TOH trends.
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.
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.
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.
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.
Irina Petropavlovskikh, Martine De Mazière, Anne M. Thompson, Jeannette D. Wild, James W. Hannigan, Henry B. Selkirk, Reem A. Hannun, Wolfgang Steinbrecht, Jean-Christopher Lambert, Roeland Van Malderen, Elizabeth Asher, Raul R. Cordero, Sophie Godin-Beekmann, Daan Hubert, Sergey Khaykin, Karin Kreher, Thierry Leblanc, Emmanuel Mahieu, Eliane Maillard Barras, Glen McConville, Gerald Nedoluha, Ivan Ortega, Alberto Redondas Marrero, Gunther Seckmeyer, Ryan M. Stauffer, Sarah A. Strode, Kim Strong, Takafumi Sugita, Michel Van Roozendael, Voltaire Velazco, Corinne Vigouroux, and Bärbel Vogel
Atmos. Chem. Phys., 26, 8637–8675, https://doi.org/10.5194/acp-26-8637-2026, https://doi.org/10.5194/acp-26-8637-2026, 2026
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This introduction to the special issue "Achievements and perspectives of the Network for the Detection of Atmospheric Composition Change after 35 years of operation” provides an overview of important research findings achieved under the NDACC objectives. The future of NDACC is discussed in the light of the evolution of the scientific questions, evolving collaborations with partners and Cooperating Networks, and the current landscape of gaps in satellite and ground-based observations.
Hantao Wang, Marc L. Serre, Kazuyuki Miyazaki, Juan Cuesta, Jerry R. Ziemke, and J. Jason West
EGUsphere, https://doi.org/10.5194/egusphere-2026-2812, https://doi.org/10.5194/egusphere-2026-2812, 2026
This preprint is open for discussion and under review for Atmospheric Chemistry and Physics (ACP).
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Ground-level ozone poses a significant health risk, yet ground monitors are sparse and satellites lack surface sensitivity. Here we develop a framework to infer surface ozone directly from satellite observations. By leveraging vertical profiles from balloons and aircraft and using chemical reanalysis vertical ratios, we significantly improved the accuracy of ozone estimates. Our 2005–2022 global dataset provides a valuable ground-level ozone background field for regions lacking ground networks.
Jay R. Herman and Jerald Ziemke
EGUsphere, https://doi.org/10.5194/egusphere-2026-1631, https://doi.org/10.5194/egusphere-2026-1631, 2026
This preprint is open for discussion and under review for Atmospheric Measurement Techniques (AMT).
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The amount of reflected sunlight has been estimated by two independent satellite observations, EPIC (Earth Polychromatic Imaging Camera) and CERES (Clouds and the Earth's Radiant Energy System). Both measurements show that the amount of reflected light from the Earth has decreased since 2016 and with a faster rate of decrease since 2020. The decreased reflectivity enhances the effect of global warming from increased amounts of carbon dioxide and methane in the atmosphere.
Caterina Mogno, Peter R. Colarco, Allison B. Collow, Sampa Das, Sarah A. Strode, Vanessa Valenti, Michael E. Manyin, Qing Liang, Luke Oman, Stephen D. Steenrod, and K. Emma Knowland
Atmos. Chem. Phys., 26, 3025–3047, https://doi.org/10.5194/acp-26-3025-2026, https://doi.org/10.5194/acp-26-3025-2026, 2026
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We investigated a climate model's ability to simulate atmospheric aerosols focusing on the relationship between mass and optical properties, by comparing predictions with observations. Our analysis revealed that model errors in aerosol scattering primarily stem from inaccurate particle mass concentrations and relative humidity, rather than flawed optical property assumptions in the model. These findings point out improvements for enhancing the accuracy for aerosols representation in our model.
Sean Davis, William Ball, Yue Jia, Gabriel Chiodo, Justin Alsing, James Keeble, Hideharu Akiyoshi, Carlo Arosio, Ewa Bednarz, Andreas Chrysanthou, Melanie Coldewey-Egbers, Robert Damadeo, Sandip Dhomse, Mohamadou Diallo, Simone Dietmuller, Roland Eichinger, Stacey Frith, Birgit Hassler, Michaela Hegglin, Daan Hubert, Patrick Jöckel, Béatrice Josse, Natalya Kramarova, Diego Loyola, Eliane Maillard Barras, Marion Marchand, Olaf Morgenstern, David Plummer, Robert Portmann, Karen Rosenlof, Alexei Rozanov, Viktoria Sofieva, Johannes Staehelin, Timofei Sukhodolov, Kleareti Tourpali, Ronald Van der A, H. J. Ray Wang, Krzysztof Wargan, Shingo Watanabe, Mark Weber, Jeannette Wild, Yousuke Yamashita, and Jerry Ziemke
EGUsphere, https://doi.org/10.5194/egusphere-2026-532, https://doi.org/10.5194/egusphere-2026-532, 2026
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This study investigates how tropical ozone levels have changed since 2000 in chemistry climate models and satellite observations to determine how well they agree with one another, and to see if current trends can help predict future levels. At some, satellite records disagree significantly on the magnitude of ozone changes. The study shows a connection between recent ozone trends and future ozone levels, suggesting that satellite measurements could help constrain future ozone changes.
Amir H. Souri, Gonzalo González Abad, Bryan N. Duncan, and Luke D. Oman
Atmos. Chem. Phys., 26, 809–837, https://doi.org/10.5194/acp-26-809-2026, https://doi.org/10.5194/acp-26-809-2026, 2026
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We create long-term maps of PO3 magnitudes along with their corresponding sensitivity maps. This is achieved using a deep learning parameterization method that relies on satellite data, atmospheric models, and ground-based remote sensing. Our approach provides more quantitative information than commonly used methods that depend on ratio-based indicators (such as HCHO/NO2). Additionally, our method considers light and water vapor, making it suitable for applications with GEO satellites.
Anne M. Thompson, Ryan M. Stauffer, Debra E. Kollonige, Jerald R. Ziemke, Bryan J. Johnson, Gary A. Morris, Patrick Cullis, María Cazorla, Jorge Andres Diaz, Ankie Piters, Igor Nedeljkovic, Truus Warsodikromo, Francisco Raimundo Silva, E. Thomas Northam, Patrick Benjamin, Thumeka Mkololo, Tshidi Machinini, Christian Félix, Gonzague Romanens, Syprose Nyadida, Jérôme Brioude, Stéphanie Evan, Jean-Marc Metzger, Ambun Dindang, Yuzaimi B. Mahat, Mohan Kumar Sammathuria, Norazura Binti Zakaria, Ninong Komala, Shin-Ya Ogino, Nguyen Thi Quyen, Francis S. Mani, Miriama Vuiyasawa, David Nardini, Matthew Martinsen, Darryl T. Kuniyuki, Katrin Müller, Pawel Wolff, and Bastien Sauvage
Atmos. Chem. Phys., 25, 18475–18507, https://doi.org/10.5194/acp-25-18475-2025, https://doi.org/10.5194/acp-25-18475-2025, 2025
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Ozone profile trends from SHADOZ sondes and IAGOS aircraft show that ozone in the tropical free troposphere (FT) is not growing fast except over equatorial SE Asia. This agrees with HEGIFTOM (Van Malderen et al., 2025), Stauffer et al. (2024) and Gaudel et al. (2024) TOAR-II papers. Other findings are as follows: (1) our trends are independent of method (QR, MLR) and (2) sample number (SN) (i.e., SHADOZ sampling is sufficient), and (3) all ground-based trends constitute the gold standard for satellite-derived trends.
Arno Keppens, Daan Hubert, José Granville, Oindrila Nath, Jean-Christopher Lambert, Catherine Wespes, Pierre-François Coheur, Cathy Clerbaux, Anne Boynard, Richard Siddans, Barry Latter, Brian Kerridge, Serena Di Pede, Pepijn Veefkind, Juan Cuesta, Gaelle Dufour, Klaus-Peter Heue, Melanie Coldewey-Egbers, Diego Loyola, Andrea Orfanoz-Cheuquelaf, Swathi Maratt Satheesan, Kai-Uwe Eichmann, Alexei Rozanov, Viktoria F. Sofieva, Jerald R. Ziemke, Antje Inness, Roeland Van Malderen, and Lars Hoffmann
Atmos. Meas. Tech., 18, 6893–6916, https://doi.org/10.5194/amt-18-6893-2025, https://doi.org/10.5194/amt-18-6893-2025, 2025
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The first Tropospheric Ozone Assessment Report (TOAR) encountered discrepancies between several satellite sensors’ estimates of the distribution and change of ozone in the free troposphere. Therefore, contributing to the second TOAR, we harmonise as much as possible the observational perspective of sixteen tropospheric ozone products from satellites. This only partially accounts for the observed discrepancies, with a reduction of 10–40 % of the inter-product dispersion upon harmonisation.
Huisheng Bian, Sarah Strode, Mian Chin, Fan Li, Andrea Molad, Peter R. Colarco, and Hongbin Yu
EGUsphere, https://doi.org/10.5194/egusphere-2025-4501, https://doi.org/10.5194/egusphere-2025-4501, 2025
Preprint archived
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We study the North Pacific westerly jet (NPWJ) using four reanalysis datasets and eight CMIP6 models. Our results show that between 1980 and 2019, the NPWJ core oscillates seasonally between north and south, weakening and shifting northward in summer and autumn. Single-forcing simulations further reveal aerosol forcing as the main driver. Incorporating interacting chemistry and time-varying ozone radiative forcing into Earth system models is crucial for simulating long-term atmospheric dynamics.
Suvarna Fadnavis, Yasin Elshorbany, Jerald Ziemke, Brice Barret, Alexandru Rap, P. R. Satheesh Chandran, Richard J. Pope, Vijay Sagar, Domenico Taraborrelli, Eric Le Flochmoen, Juan Cuesta, Catherine Wespes, Folkert Boersma, Isolde Glissenaar, Isabelle De Smedt, Michel Van Roozendael, Hervé Petetin, and Isidora Anglou
Atmos. Chem. Phys., 25, 8229–8254, https://doi.org/10.5194/acp-25-8229-2025, https://doi.org/10.5194/acp-25-8229-2025, 2025
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Satellites and model simulations show enhancement in tropospheric ozone, which is highly impacted by human-produced nitrous oxides compared to volatile organic compounds. The increased amount of ozone enhances ozone radiative forcing. The ozone enhancement and associated radiative forcing are the highest over South and East Asia. The emissions of nitrous oxides show a higher influence on shifting ozone photochemical regimes than volatile organic compounds.
Carlo Arosio, Viktoria Sofieva, Andrea Orfanoz-Cheuquelaf, Alexei Rozanov, Klaus-Peter Heue, Diego Loyola, Edward Malina, Ryan M. Stauffer, David Tarasick, Roeland Van Malderen, Jerry R. Ziemke, and Mark Weber
Atmos. Meas. Tech., 18, 3247–3265, https://doi.org/10.5194/amt-18-3247-2025, https://doi.org/10.5194/amt-18-3247-2025, 2025
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Tropospheric ozone affects air quality and climate, being a pollutant and a greenhouse gas. We analyze satellite data of tropospheric ozone columns obtained by combining two types of observations: one providing stratospheric and the other total ozone. We compare common climatological features and study the influence of the tropopause (troposphere to stratosphere boundary) on the results. We also examine trends over the last 20 years and compare satellite data with ozonesondes to identify drifts.
Amir H. Souri, Gonzalo González Abad, Glenn M. Wolfe, Tijl Verhoelst, Corinne Vigouroux, Gaia Pinardi, Steven Compernolle, Bavo Langerock, Bryan N. Duncan, and Matthew S. Johnson
Atmos. Chem. Phys., 25, 2061–2086, https://doi.org/10.5194/acp-25-2061-2025, https://doi.org/10.5194/acp-25-2061-2025, 2025
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We establish a simple yet robust relationship between ozone production rates and geophysical parameters obtained from several intensive atmospheric composition campaigns. We show that satellite remote sensing data can effectively constrain these parameters, enabling us to produce the first global maps of ozone production rates with unprecedented resolution.
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
Atmos. Chem. Phys., 25, 597–624, https://doi.org/10.5194/acp-25-597-2025, https://doi.org/10.5194/acp-25-597-2025, 2025
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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 well matched by model trends. We find that changes in modeled industrial CO surface emissions lead to better model agreement with observed slight decreases in upper-tropospheric CO.
Bryan N. Duncan, Daniel C. Anderson, Arlene M. Fiore, Joanna Joiner, Nickolay A. Krotkov, Can Li, Dylan B. Millet, Julie M. Nicely, Luke D. Oman, Jason M. St. Clair, Joshua D. Shutter, Amir H. Souri, Sarah A. Strode, Brad Weir, Glenn M. Wolfe, Helen M. Worden, and Qindan Zhu
Atmos. Chem. Phys., 24, 13001–13023, https://doi.org/10.5194/acp-24-13001-2024, https://doi.org/10.5194/acp-24-13001-2024, 2024
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Trace gases emitted to or formed within the atmosphere may be chemically or physically removed from the atmosphere. One trace gas, the hydroxyl radical (OH), is responsible for initiating the chemical removal of many trace gases, including some greenhouse gases. Despite its importance, scientists have not been able to adequately measure OH. In this opinion piece, we discuss promising new methods to indirectly constrain OH using satellite data of trace gases that control the abundance of OH.
Yasin Elshorbany, Jerald R. Ziemke, Sarah Strode, Hervé Petetin, Kazuyuki Miyazaki, Isabelle De Smedt, Kenneth Pickering, Rodrigo J. Seguel, Helen Worden, Tamara Emmerichs, Domenico Taraborrelli, Maria Cazorla, Suvarna Fadnavis, Rebecca R. Buchholz, Benjamin Gaubert, Néstor Y. Rojas, Thiago Nogueira, Thérèse Salameh, and Min Huang
Atmos. Chem. Phys., 24, 12225–12257, https://doi.org/10.5194/acp-24-12225-2024, https://doi.org/10.5194/acp-24-12225-2024, 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 CO, as well as ozonesonde data and model simulations.
Pinchas Nürnberg, Sarah A. Strode, and Ralf Sussmann
Atmos. Chem. Phys., 24, 10001–10012, https://doi.org/10.5194/acp-24-10001-2024, https://doi.org/10.5194/acp-24-10001-2024, 2024
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We created a set of scaling factors describing the diurnal increase in stratospheric nitrogen oxides above Zugspitze, Germany. We used these factors to validate recently published model simulation data. On the one hand, this validation enables the use of the validated data to better understand the stratospheric photochemistry. On the other hand, it can improve satellite validation, which has implications for the understanding of urban smog events and other pollution events in the troposphere.
Audrey Gaudel, Ilann Bourgeois, Meng Li, Kai-Lan Chang, Jerald Ziemke, Bastien Sauvage, Ryan M. Stauffer, Anne M. Thompson, Debra E. Kollonige, Nadia Smith, Daan Hubert, Arno Keppens, Juan Cuesta, Klaus-Peter Heue, Pepijn Veefkind, Kenneth Aikin, Jeff Peischl, Chelsea R. Thompson, Thomas B. Ryerson, Gregory J. Frost, Brian C. McDonald, and Owen R. Cooper
Atmos. Chem. Phys., 24, 9975–10000, https://doi.org/10.5194/acp-24-9975-2024, https://doi.org/10.5194/acp-24-9975-2024, 2024
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The study examines tropical tropospheric ozone changes. In situ data from 1994–2019 display increased ozone, notably over India, Southeast Asia, and Malaysia and Indonesia. Sparse in situ data limit trend detection for the 15-year period. In situ and satellite data, with limited sampling, struggle to consistently detect trends. Continuous observations are vital over the tropical Pacific Ocean, Indian Ocean, western Africa, and South Asia for accurate ozone trend estimation in these regions.
Amir H. Souri, Bryan N. Duncan, Sarah A. Strode, Daniel C. Anderson, Michael E. Manyin, Junhua Liu, Luke D. Oman, Zhen Zhang, and Brad Weir
Atmos. Chem. Phys., 24, 8677–8701, https://doi.org/10.5194/acp-24-8677-2024, https://doi.org/10.5194/acp-24-8677-2024, 2024
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We explore a new method of using the wealth of information obtained from satellite observations of Aura OMI NO2, HCHO, and MERRA-2 reanalysis in NASA’s GEOS model equipped with an efficient tropospheric OH (TOH) estimator to enhance the representation of TOH spatial distribution and its long-term trends. This new framework helps us pinpoint regional inaccuracies in TOH and differentiate between established prior knowledge and newly acquired information from satellites on TOH trends.
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.
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.
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.
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.
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.
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.
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Short summary
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.
A low bias in carbon monoxide (CO) at northern latitudes is a common feature of chemistry...
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