Articles | Volume 16, issue 9
https://doi.org/10.5194/acp-16-5721-2016
© Author(s) 2016. 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-16-5721-2016
© Author(s) 2016. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Research article
| 
10 May 2016
Research article |
| 10 May 2016
Ozone variability in the troposphere and the stratosphere from the first 6 years of IASI observations (2008–2013)
Catherine Wespes
CORRESPONDING AUTHOR
Spectroscopie de l'Atmosphère, Service de Chimie Quantique et
Photophysique, Université Libre de Bruxelles (U.L.B.), Brussels, Belgium
Daniel Hurtmans
Spectroscopie de l'Atmosphère, Service de Chimie Quantique et
Photophysique, Université Libre de Bruxelles (U.L.B.), Brussels, Belgium
Louisa K. Emmons
National Center for Atmospheric Research, Boulder, CO, USA
Sarah Safieddine
Sorbonne Universités, UPMC Univ. Paris 06, Université
Versailles St-Quentin, CNRS/INSU, LATMOS-IPSL, Paris, France
now at: Department of Civil and Environmental Engineering, Institute of
Technology, Cambridge, Massachusetts, USA
Cathy Clerbaux
Spectroscopie de l'Atmosphère, Service de Chimie Quantique et
Photophysique, Université Libre de Bruxelles (U.L.B.), Brussels, Belgium
Sorbonne Universités, UPMC Univ. Paris 06, Université
Versailles St-Quentin, CNRS/INSU, LATMOS-IPSL, Paris, France
David P. Edwards
National Center for Atmospheric Research, Boulder, CO, USA
Pierre-François Coheur
Spectroscopie de l'Atmosphère, Service de Chimie Quantique et
Photophysique, Université Libre de Bruxelles (U.L.B.), Brussels, Belgium
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This preprint is open for discussion and under review for Atmospheric Measurement Techniques (AMT).
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Using IASI global infrared measurements, we retrieve nitrous acid (HONO) in fire plumes from space. We detect large enhancements of pyrogenic HONO worldwide, especially from intense wildfires at Northern Hemisphere mid- and high latitudes. Predominance of IASI nighttime over daytime measurements sheds light on HONO's extended lifetime and secondary formation during long-range transport in smoke plumes. Our findings deepen the understanding of atmospheric HONO, crucial for air quality assessment.
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Richard J. Pope, Alexandru Rap, Matilda A. Pimlott, Brice Barret, Eric Le Flochmoen, Brian J. Kerridge, Richard Siddans, Barry G. Latter, Lucy J. Ventress, Anne Boynard, Christian Retscher, Wuhu Feng, Richard Rigby, Sandip S. Dhomse, Catherine Wespes, and Martyn P. Chipperfield
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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.
Lieven Clarisse, Bruno Franco, Martin Van Damme, Tommaso Di Gioacchino, Juliette Hadji-Lazaro, Simon Whitburn, Lara Noppen, Daniel Hurtmans, Cathy Clerbaux, and Pierre Coheur
Atmos. Meas. Tech., 16, 5009–5028, https://doi.org/10.5194/amt-16-5009-2023, https://doi.org/10.5194/amt-16-5009-2023, 2023
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Ammonia is an important atmospheric pollutant. This article presents version 4 of the algorithm which retrieves ammonia abundances from the infrared measurements of the satellite sounder IASI. A measurement operator is introduced that can emulate the measurements (so-called averaging kernels) and measurement uncertainty is better characterized. Several other changes to the product itself are also documented, most of which improve the temporal consistency of the 2007–2022 IASI NH3 dataset.
Wenfu Tang, Louisa K. Emmons, Helen M. Worden, Rajesh Kumar, Cenlin He, Benjamin Gaubert, Zhonghua Zheng, Simone Tilmes, Rebecca R. Buchholz, Sara-Eva Martinez-Alonso, Claire Granier, Antonin Soulie, Kathryn McKain, Bruce C. Daube, Jeff Peischl, Chelsea Thompson, and Pieternel Levelt
Geosci. Model Dev., 16, 6001–6028, https://doi.org/10.5194/gmd-16-6001-2023, https://doi.org/10.5194/gmd-16-6001-2023, 2023
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The new MUSICAv0 model enables the study of atmospheric chemistry across all relevant scales. We develop a MUSICAv0 grid for Africa. We evaluate MUSICAv0 with observations and compare it with a previously used model – WRF-Chem. Overall, the performance of MUSICAv0 is comparable to WRF-Chem. Based on model–satellite discrepancies, we find that future field campaigns in an eastern African region (30°E–45°E, 5°S–5°N) could substantially improve the predictive skill of air quality models.
Rui Wang, Da Pan, Xuehui Guo, Kang Sun, Lieven Clarisse, Martin Van Damme, Pierre-François Coheur, Cathy Clerbaux, Melissa Puchalski, and Mark A. Zondlo
Atmos. Chem. Phys., 23, 13217–13234, https://doi.org/10.5194/acp-23-13217-2023, https://doi.org/10.5194/acp-23-13217-2023, 2023
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Ammonia (NH3) is a key precursor for fine particulate matter (PM2.5) and a primary form of reactive nitrogen, yet it has sparse ground measurements. We perform the first comprehensive comparison between ground observations and satellite retrievals in the US, demonstrating that satellite NH3 data can help fill spatial gaps in the current ground monitoring networks. Trend analyses using both datasets highlight increasing NH3 trends across the US, including the NH3 hotspots and urban areas.
Maria Val Martin, Elena Blanc-Betes, Ka Ming Fung, Euripides P. Kantzas, Ilsa B. Kantola, Isabella Chiaravalloti, Lyla L. Taylor, Louisa K. Emmons, William R. Wieder, Noah J. Planavsky, Michael D. Masters, Evan H. DeLucia, Amos P. K. Tai, and David J. Beerling
Geosci. Model Dev., 16, 5783–5801, https://doi.org/10.5194/gmd-16-5783-2023, https://doi.org/10.5194/gmd-16-5783-2023, 2023
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Enhanced rock weathering (ERW) is a CO2 removal strategy that involves applying crushed rocks (e.g., basalt) to agricultural soils. However, unintended processes within the N cycle due to soil pH changes may affect the climate benefits of C sequestration. ERW could drive changes in soil emissions of non-CO2 GHGs (N2O) and trace gases (NO and NH3) that may affect air quality. We present a new improved N cycling scheme for the land model (CLM5) to evaluate ERW effects on soil gas N emissions.
Rimal Abeed, Camille Viatte, William C. Porter, Nikolaos Evangeliou, Cathy Clerbaux, Lieven Clarisse, Martin Van Damme, Pierre-François Coheur, and Sarah Safieddine
Atmos. Chem. Phys., 23, 12505–12523, https://doi.org/10.5194/acp-23-12505-2023, https://doi.org/10.5194/acp-23-12505-2023, 2023
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Ammonia emissions from agricultural activities will inevitably increase with the rise in population. We use a variety of datasets (satellite, reanalysis, and model simulation) to calculate the first regional map of ammonia emission potential during the start of the growing season in Europe. We then apply our developed method using a climate model to show the effect of the temperature increase on future ammonia columns under two possible climate scenarios.
Christine Wiedinmyer, Yosuke Kimura, Elena C. McDonald-Buller, Louisa K. Emmons, Rebecca R. Buchholz, Wenfu Tang, Keenan Seto, Maxwell B. Joseph, Kelley C. Barsanti, Annmarie G. Carlton, and Robert Yokelson
Geosci. Model Dev., 16, 3873–3891, https://doi.org/10.5194/gmd-16-3873-2023, https://doi.org/10.5194/gmd-16-3873-2023, 2023
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The Fire INventory from NCAR (FINN) provides daily global estimates of emissions from open fires based on satellite detections of hot spots. This version has been updated to apply MODIS and VIIRS satellite fire detection and better represents both large and small fires. FINNv2.5 generates more emissions than FINNv1 and is in general agreement with other fire emissions inventories. The new estimates are consistent with satellite observations, but uncertainties remain regionally and by pollutant.
Duseong S. Jo, Simone Tilmes, Louisa K. Emmons, Siyuan Wang, and Francis Vitt
Geosci. Model Dev., 16, 3893–3906, https://doi.org/10.5194/gmd-16-3893-2023, https://doi.org/10.5194/gmd-16-3893-2023, 2023
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A new simple secondary organic aerosol (SOA) scheme has been developed for the Community Atmosphere Model (CAM) based on the complex SOA scheme in CAM with detailed chemistry (CAM-chem). The CAM with the new SOA scheme shows better agreements with CAM-chem in terms of aerosol concentrations and radiative fluxes, which ensures more consistent results between different compsets in the Community Earth System Model. The new SOA scheme also has technical advantages for future developments.
Wenfu Tang, Simone Tilmes, David M. Lawrence, Fang Li, Cenlin He, Louisa K. Emmons, Rebecca R. Buchholz, and Lili Xia
Atmos. Chem. Phys., 23, 5467–5486, https://doi.org/10.5194/acp-23-5467-2023, https://doi.org/10.5194/acp-23-5467-2023, 2023
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Globally, total wildfire burned area is projected to increase over the 21st century under scenarios without geoengineering and decrease under the two geoengineering scenarios. Geoengineering reduces fire by decreasing surface temperature and wind speed and increasing relative humidity and soil water. However, geoengineering also yields reductions in precipitation, which offset some of the fire reduction.
Adrien Vu Van, Anne Boynard, Pascal Prunet, Dominique Jolivet, Olivier Lezeaux, Patrice Henry, Claude Camy-Peyret, Lieven Clarisse, Bruno Franco, Pierre-François Coheur, and Cathy Clerbaux
Atmos. Meas. Tech., 16, 2107–2127, https://doi.org/10.5194/amt-16-2107-2023, https://doi.org/10.5194/amt-16-2107-2023, 2023
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With its near-real-time observations and good horizontal coverage, the Infrared Atmospheric Sounding Interferometer (IASI) instrument can contribute to the monitoring systems for a systematic and continuous detection of exceptional atmospheric events such as fires, anthropogenic pollution episodes, volcanic eruptions, or industrial releases. In this paper, a new approach is described for the detection and characterization of unexpected events in terms of trace gases using IASI radiance spectra.
Florent Tencé, Julien Jumelet, Marie Bouillon, David Cugnet, Slimane Bekki, Sarah Safieddine, Philippe Keckhut, and Alain Sarkissian
Atmos. Chem. Phys., 23, 431–451, https://doi.org/10.5194/acp-23-431-2023, https://doi.org/10.5194/acp-23-431-2023, 2023
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Polar stratospheric clouds (PSCs) are critical precursors to stratospheric ozone depletion, and measurement-driven classifications remain a key to accurate cloud modelling. We present PSC lidar observations conducted at the French Antarctic station Dumont d'Urville between 2007 and 2020. This dataset is analyzed using typical PSC classification schemes. We present a PSC climatology along with a significant and slightly negative 14-year trend of PSC occurences of −4.6 PSC days per decade.
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.
Thibaud M. Fritz, Sebastian D. Eastham, Louisa K. Emmons, Haipeng Lin, Elizabeth W. Lundgren, Steve Goldhaber, Steven R. H. Barrett, and Daniel J. Jacob
Geosci. Model Dev., 15, 8669–8704, https://doi.org/10.5194/gmd-15-8669-2022, https://doi.org/10.5194/gmd-15-8669-2022, 2022
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We bring the state-of-the-science chemistry module GEOS-Chem into the Community Earth System Model (CESM). We show that some known differences between results from GEOS-Chem and CESM's CAM-chem chemistry module may be due to the configuration of model meteorology rather than inherent differences in the model chemistry. This is a significant step towards a truly modular Earth system model and allows two strong but currently separate research communities to benefit from each other's advances.
Simon Whitburn, Lieven Clarisse, Marc Crapeau, Thomas August, Tim Hultberg, Pierre François Coheur, and Cathy Clerbaux
Atmos. Meas. Tech., 15, 6653–6668, https://doi.org/10.5194/amt-15-6653-2022, https://doi.org/10.5194/amt-15-6653-2022, 2022
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With more than 15 years of measurements, the IASI radiance dataset is becoming a reference climate data record. Its exploitation for satellite applications requires an accurate and unbiased detection of cloud scenes. Here, we present a new cloud detection algorithm for IASI that is both sensitive and consistent over time. It is based on the use of a neural network, relying on IASI radiance information only and taking as a reference the last version of the operational IASI L2 cloud product.
Longlei Li, Natalie M. Mahowald, Jasper F. Kok, Xiaohong Liu, Mingxuan Wu, Danny M. Leung, Douglas S. Hamilton, Louisa K. Emmons, Yue Huang, Neil Sexton, Jun Meng, and Jessica Wan
Geosci. Model Dev., 15, 8181–8219, https://doi.org/10.5194/gmd-15-8181-2022, https://doi.org/10.5194/gmd-15-8181-2022, 2022
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This study advances mineral dust parameterizations in the Community Atmospheric Model (CAM; version 6.1). Efforts include 1) incorporating a more physically based dust emission scheme; 2) updating the dry deposition scheme; and 3) revising the gravitational settling velocity to account for dust asphericity. Substantial improvements achieved with these updates can help accurately quantify dust–climate interactions using CAM, such as the dust-radiation and dust–cloud interactions.
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.
Catherine Wespes, Gaetane Ronsmans, Lieven Clarisse, Susan Solomon, Daniel Hurtmans, Cathy Clerbaux, and Pierre-François Coheur
Atmos. Chem. Phys., 22, 10993–11007, https://doi.org/10.5194/acp-22-10993-2022, https://doi.org/10.5194/acp-22-10993-2022, 2022
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The first 10-year data record (2008–2017) of HNO3 total columns measured by the IASI-A/MetOp infrared sounder is exploited to monitor the relationship between the temperature decrease and the HNO3 loss observed each year in the Antarctic stratosphere during the polar night. We verify the recurrence of specific regimes in the cycle of IASI HNO3 and identify the day and the 50 hPa temperature (
drop temperature) corresponding to the onset of denitrification in Antarctic winter for each year.
Marie Bouillon, Sarah Safieddine, Simon Whitburn, Lieven Clarisse, Filipe Aires, Victor Pellet, Olivier Lezeaux, Noëlle A. Scott, Marie Doutriaux-Boucher, and Cathy Clerbaux
Atmos. Meas. Tech., 15, 1779–1793, https://doi.org/10.5194/amt-15-1779-2022, https://doi.org/10.5194/amt-15-1779-2022, 2022
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The IASI instruments have been observing Earth since 2007. We use a neural network to retrieve atmospheric temperatures. This new temperature data record is validated against other datasets and shows good agreement. We use this new dataset to compute trends over the 2008–2020 period. We found a warming of the troposphere, more important at the poles. In the stratosphere, we found that temperatures decrease everywhere except at the South Pole. The cooling is more pronounced at the South pole.
Jonathan E. Hickman, Niels Andela, Enrico Dammers, Lieven Clarisse, Pierre-François Coheur, Martin Van Damme, Courtney A. Di Vittorio, Money Ossohou, Corinne Galy-Lacaux, Kostas Tsigaridis, and Susanne E. Bauer
Atmos. Chem. Phys., 21, 16277–16291, https://doi.org/10.5194/acp-21-16277-2021, https://doi.org/10.5194/acp-21-16277-2021, 2021
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Ammonia (NH3) gas emitted from soils and biomass burning contributes to particulate air pollution. We used satellite observations of the atmosphere over Africa to show that declines in NH3 concentrations over South Sudan's Sudd wetland in 2008–2017 are related to variation in wetland extent. We also find NH3 concentrations increased in West Africa as a result of biomass burning and increased in the Lake Victoria region, likely due to agricultural expansion and intensification.
Xinxin Ye, Pargoal Arab, Ravan Ahmadov, Eric James, Georg A. Grell, Bradley Pierce, Aditya Kumar, Paul Makar, Jack Chen, Didier Davignon, Greg R. Carmichael, Gonzalo Ferrada, Jeff McQueen, Jianping Huang, Rajesh Kumar, Louisa Emmons, Farren L. Herron-Thorpe, Mark Parrington, Richard Engelen, Vincent-Henri Peuch, Arlindo da Silva, Amber Soja, Emily Gargulinski, Elizabeth Wiggins, Johnathan W. Hair, Marta Fenn, Taylor Shingler, Shobha Kondragunta, Alexei Lyapustin, Yujie Wang, Brent Holben, David M. Giles, and Pablo E. Saide
Atmos. Chem. Phys., 21, 14427–14469, https://doi.org/10.5194/acp-21-14427-2021, https://doi.org/10.5194/acp-21-14427-2021, 2021
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Wildfire smoke has crucial impacts on air quality, while uncertainties in the numerical forecasts remain significant. We present an evaluation of 12 real-time forecasting systems. Comparison of predicted smoke emissions suggests a large spread in magnitudes, with temporal patterns deviating from satellite detections. The performance for AOD and surface PM2.5 and their discrepancies highlighted the role of accurately represented spatiotemporal emission profiles in improving smoke forecasts.
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.
Haipeng Lin, Daniel J. Jacob, Elizabeth W. Lundgren, Melissa P. Sulprizio, Christoph A. Keller, Thibaud M. Fritz, Sebastian D. Eastham, Louisa K. Emmons, Patrick C. Campbell, Barry Baker, Rick D. Saylor, and Raffaele Montuoro
Geosci. Model Dev., 14, 5487–5506, https://doi.org/10.5194/gmd-14-5487-2021, https://doi.org/10.5194/gmd-14-5487-2021, 2021
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Emissions are a central component of atmospheric chemistry models. The Harmonized Emissions Component (HEMCO) is a software component for computing emissions from a user-selected ensemble of emission inventories and algorithms. It allows users to select, add, and scale emissions from different sources through a configuration file with no change to the model source code. We demonstrate the implementation of HEMCO in several models, all sharing the same HEMCO core code and database library.
Simon Rosanka, Bruno Franco, Lieven Clarisse, Pierre-François Coheur, Andrea Pozzer, Andreas Wahner, and Domenico Taraborrelli
Atmos. Chem. Phys., 21, 11257–11288, https://doi.org/10.5194/acp-21-11257-2021, https://doi.org/10.5194/acp-21-11257-2021, 2021
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The strong El Niño in 2015 led to a particular dry season in Indonesia and favoured severe peatland fires. The smouldering conditions of these fires and the high carbon content of peat resulted in high volatile organic compound (VOC) emissions. By using a comprehensive atmospheric model, we show that these emissions have a significant impact on the tropospheric composition and oxidation capacity. These emissions are transported into to the lower stratosphere, resulting in a depletion of ozone.
Tamara Emmerichs, Bruno Franco, Catherine Wespes, Vinod Kumar, Andrea Pozzer, Simon Rosanka, and Domenico Taraborrelli
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2021-584, https://doi.org/10.5194/acp-2021-584, 2021
Revised manuscript not accepted
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Near-surface ozone is a harmful air pollutant and it is strongly affected by radical reactions and surface-atmosphere exchanges which in turn are modulated, directly and indirectly, by weather. Understanding the impact of weather on ozone, and air quality, is thus important also in view of weather extremes. The inclusion of additional ozone-weather links in the global model yields a 2-fold reduction of the ozone bias towards satellite observations.
Simon Rosanka, Rolf Sander, Bruno Franco, Catherine Wespes, Andreas Wahner, and Domenico Taraborrelli
Atmos. Chem. Phys., 21, 9909–9930, https://doi.org/10.5194/acp-21-9909-2021, https://doi.org/10.5194/acp-21-9909-2021, 2021
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In-cloud destruction of ozone depends on hydroperoxyl radicals in cloud droplets, where they are produced by oxygenated volatile organic compound (OVOC) oxygenation. Only rudimentary representations of these processes, if any, are currently available in global atmospheric models. By using a comprehensive atmospheric model that includes a complex in-cloud OVOC oxidation scheme, we show that atmospheric oxidants are reduced and models ignoring this process will underpredict clouds as ozone sinks.
Wenfu Tang, David P. Edwards, Louisa K. Emmons, Helen M. Worden, Laura M. Judd, Lok N. Lamsal, Jassim A. Al-Saadi, Scott J. Janz, James H. Crawford, Merritt N. Deeter, Gabriele Pfister, Rebecca R. Buchholz, Benjamin Gaubert, and Caroline R. Nowlan
Atmos. Meas. Tech., 14, 4639–4655, https://doi.org/10.5194/amt-14-4639-2021, https://doi.org/10.5194/amt-14-4639-2021, 2021
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We use high-resolution airborne mapping spectrometer measurements to assess sub-grid variability within satellite pixels over urban regions. The sub-grid variability within satellite pixels increases with increasing satellite pixel sizes. Temporal variability within satellite pixels decreases with increasing satellite pixel sizes. This work is particularly relevant and useful for future satellite design, satellite data interpretation, and point-grid data comparisons.
Yaman Liu, Xinyi Dong, Minghuai Wang, Louisa K. Emmons, Yawen Liu, Yuan Liang, Xiao Li, and Manish Shrivastava
Atmos. Chem. Phys., 21, 8003–8021, https://doi.org/10.5194/acp-21-8003-2021, https://doi.org/10.5194/acp-21-8003-2021, 2021
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Secondary organic aerosol (SOA) is considered one of the most important uncertainties in climate modeling. We evaluate SOA performance in the Community Earth System Model version 2.1 (CESM2.1) configured with the Community Atmosphere Model version 6 with chemistry (CAM6-Chem) through a long-term simulation (1988–2019) with observations in the United States, which indicates monoterpene-formed SOA contributes most to the overestimation of SOA at the surface and underestimation in the upper air.
Karn Vohra, Eloise A. Marais, Shannen Suckra, Louisa Kramer, William J. Bloss, Ravi Sahu, Abhishek Gaur, Sachchida N. Tripathi, Martin Van Damme, Lieven Clarisse, and Pierre-F. Coheur
Atmos. Chem. Phys., 21, 6275–6296, https://doi.org/10.5194/acp-21-6275-2021, https://doi.org/10.5194/acp-21-6275-2021, 2021
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We find satellite observations of atmospheric composition generally reproduce variability in surface air pollution, so we use their long record to estimate air quality trends in major UK and Indian cities. Our trend analysis shows that pollutants targeted with air quality policies have not declined in Delhi and Kanpur but have in London and Birmingham, with the exception of a recent and dramatic increase in reactive volatile organics in London. Unregulated ammonia has increased only in Delhi.
Pooja V. Pawar, Sachin D. Ghude, Chinmay Jena, Andrea Móring, Mark A. Sutton, Santosh Kulkarni, Deen Mani Lal, Divya Surendran, Martin Van Damme, Lieven Clarisse, Pierre-François Coheur, Xuejun Liu, Gaurav Govardhan, Wen Xu, Jize Jiang, and Tapan Kumar Adhya
Atmos. Chem. Phys., 21, 6389–6409, https://doi.org/10.5194/acp-21-6389-2021, https://doi.org/10.5194/acp-21-6389-2021, 2021
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In this study, simulations of atmospheric ammonia (NH3) with MOZART-4 and HTAP-v2 are compared with satellite (IASI) and ground-based measurements to understand the spatial and temporal variability of NH3 over two emission hotspot regions of Asia, the IGP and the NCP. Our simulations indicate that the formation of ammonium aerosols is quicker over the NCP than the IGP, leading to smaller NH3 columns over the higher NH3-emitting NCP compared to the IGP region for comparable emissions.
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).
Nikolaos Evangeliou, Yves Balkanski, Sabine Eckhardt, Anne Cozic, Martin Van Damme, Pierre-François Coheur, Lieven Clarisse, Mark W. Shephard, Karen E. Cady-Pereira, and Didier Hauglustaine
Atmos. Chem. Phys., 21, 4431–4451, https://doi.org/10.5194/acp-21-4431-2021, https://doi.org/10.5194/acp-21-4431-2021, 2021
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Ammonia, a substance that has played a key role in sustaining life, has been increasing in the atmosphere, affecting climate and humans. Understanding the reasons for this increase is important for the beneficial use of ammonia. The evolution of satellite products gives us the opportunity to calculate ammonia emissions easier. We calculated global ammonia emissions over the last 10 years, incorporated them into a chemistry model and recorded notable improvement in reproducing observations.
Paul T. Griffiths, Lee T. Murray, Guang Zeng, Youngsub Matthew Shin, N. Luke Abraham, Alexander T. Archibald, Makoto Deushi, Louisa K. Emmons, Ian E. Galbally, Birgit Hassler, Larry W. Horowitz, James Keeble, Jane Liu, Omid Moeini, Vaishali Naik, Fiona M. O'Connor, Naga Oshima, David Tarasick, Simone Tilmes, Steven T. Turnock, Oliver Wild, Paul J. Young, and Prodromos Zanis
Atmos. Chem. Phys., 21, 4187–4218, https://doi.org/10.5194/acp-21-4187-2021, https://doi.org/10.5194/acp-21-4187-2021, 2021
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We analyse the CMIP6 Historical and future simulations for tropospheric ozone, a species which is important for many aspects of atmospheric chemistry. We show that the current generation of models agrees well with observations, being particularly successful in capturing trends in surface ozone and its vertical distribution in the troposphere. We analyse the factors that control ozone and show that they evolve over the period of the CMIP6 experiments.
Duseong S. Jo, Alma Hodzic, Louisa K. Emmons, Simone Tilmes, Rebecca H. Schwantes, Michael J. Mills, Pedro Campuzano-Jost, Weiwei Hu, Rahul A. Zaveri, Richard C. Easter, Balwinder Singh, Zheng Lu, Christiane Schulz, Johannes Schneider, John E. Shilling, Armin Wisthaler, and Jose L. Jimenez
Atmos. Chem. Phys., 21, 3395–3425, https://doi.org/10.5194/acp-21-3395-2021, https://doi.org/10.5194/acp-21-3395-2021, 2021
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Secondary organic aerosol (SOA) is a major component of submicron particulate matter, but there are a lot of uncertainties in the future prediction of SOA. We used CESM 2.1 to investigate future IEPOX SOA concentration changes. The explicit chemistry predicted substantial changes in IEPOX SOA depending on the future scenario, but the parameterization predicted weak changes due to simplified chemistry, which shows the importance of correct physicochemical dependencies in future SOA prediction.
Yilin Chen, Huizhong Shen, Jennifer Kaiser, Yongtao Hu, Shannon L. Capps, Shunliu Zhao, Amir Hakami, Jhih-Shyang Shih, Gertrude K. Pavur, Matthew D. Turner, Daven K. Henze, Jaroslav Resler, Athanasios Nenes, Sergey L. Napelenok, Jesse O. Bash, Kathleen M. Fahey, Gregory R. Carmichael, Tianfeng Chai, Lieven Clarisse, Pierre-François Coheur, Martin Van Damme, and Armistead G. Russell
Atmos. Chem. Phys., 21, 2067–2082, https://doi.org/10.5194/acp-21-2067-2021, https://doi.org/10.5194/acp-21-2067-2021, 2021
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Ammonia (NH3) emissions can exert adverse impacts on air quality and ecosystem well-being. NH3 emission inventories are viewed as highly uncertain. Here we optimize the NH3 emission estimates in the US using an air quality model and NH3 measurements from the IASI satellite instruments. The optimized NH3 emissions are much higher than the National Emissions Inventory estimates in April. The optimized NH3 emissions improved model performance when evaluated against independent observation.
Shoma Yamanouchi, Camille Viatte, Kimberly Strong, Erik Lutsch, Dylan B. A. Jones, Cathy Clerbaux, Martin Van Damme, Lieven Clarisse, and Pierre-Francois Coheur
Atmos. Meas. Tech., 14, 905–921, https://doi.org/10.5194/amt-14-905-2021, https://doi.org/10.5194/amt-14-905-2021, 2021
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Ammonia (NH3) is a major source of pollution in the air. As such, there have been increasing efforts to measure the atmospheric abundance of NH3 and its spatial and temporal variability. In this study, long-term measurements of NH3 over Toronto, Canada, derived from multiscale datasets are examined. These NH3 datasets were compared to each other and to a model to better understand NH3 variability and to assess model performance.
Gillian D. Thornhill, William J. Collins, Ryan J. Kramer, Dirk Olivié, Ragnhild B. Skeie, Fiona M. O'Connor, Nathan Luke Abraham, Ramiro Checa-Garcia, Susanne E. Bauer, Makoto Deushi, Louisa K. Emmons, Piers M. Forster, Larry W. Horowitz, Ben Johnson, James Keeble, Jean-Francois Lamarque, Martine Michou, Michael J. Mills, Jane P. Mulcahy, Gunnar Myhre, Pierre Nabat, Vaishali Naik, Naga Oshima, Michael Schulz, Christopher J. Smith, Toshihiko Takemura, Simone Tilmes, Tongwen Wu, Guang Zeng, and Jie Zhang
Atmos. Chem. Phys., 21, 853–874, https://doi.org/10.5194/acp-21-853-2021, https://doi.org/10.5194/acp-21-853-2021, 2021
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This paper is a study of how different constituents in the atmosphere, such as aerosols and gases like methane and ozone, affect the energy balance in the atmosphere. Different climate models were run using the same inputs to allow an easy comparison of the results and to understand where the models differ. We found the effect of aerosols is to reduce warming in the atmosphere, but this effect varies between models. Reactions between gases are also important in affecting climate.
Benjamin Gaubert, Louisa K. Emmons, Kevin Raeder, Simone Tilmes, Kazuyuki Miyazaki, Avelino F. Arellano Jr., Nellie Elguindi, Claire Granier, Wenfu Tang, Jérôme Barré, Helen M. Worden, Rebecca R. Buchholz, David P. Edwards, Philipp Franke, Jeffrey L. Anderson, Marielle Saunois, Jason Schroeder, Jung-Hun Woo, Isobel J. Simpson, Donald R. Blake, Simone Meinardi, Paul O. Wennberg, John Crounse, Alex Teng, Michelle Kim, Russell R. Dickerson, Hao He, Xinrong Ren, Sally E. Pusede, and Glenn S. Diskin
Atmos. Chem. Phys., 20, 14617–14647, https://doi.org/10.5194/acp-20-14617-2020, https://doi.org/10.5194/acp-20-14617-2020, 2020
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This study investigates carbon monoxide pollution in East Asia during spring using a numerical model, satellite remote sensing, and aircraft measurements. We found an underestimation of emission sources. Correcting the emission bias can improve air quality forecasting of carbon monoxide and other species including ozone. Results also suggest that controlling VOC and CO emissions, in addition to widespread NOx controls, can improve ozone pollution over East Asia.
Steven T. Turnock, Robert J. Allen, Martin Andrews, Susanne E. Bauer, Makoto Deushi, Louisa Emmons, Peter Good, Larry Horowitz, Jasmin G. John, Martine Michou, Pierre Nabat, Vaishali Naik, David Neubauer, Fiona M. O'Connor, Dirk Olivié, Naga Oshima, Michael Schulz, Alistair Sellar, Sungbo Shim, Toshihiko Takemura, Simone Tilmes, Kostas Tsigaridis, Tongwen Wu, and Jie Zhang
Atmos. Chem. Phys., 20, 14547–14579, https://doi.org/10.5194/acp-20-14547-2020, https://doi.org/10.5194/acp-20-14547-2020, 2020
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A first assessment is made of the historical and future changes in air pollutants from models participating in the 6th Coupled Model Intercomparison Project (CMIP6). Substantial benefits to future air quality can be achieved in future scenarios that implement measures to mitigate climate and involve reductions in air pollutant emissions, particularly methane. However, important differences are shown between models in the future regional projection of air pollutants under the same scenario.
Audrey Fortems-Cheiney, Gaëlle Dufour, Karine Dufossé, Florian Couvidat, Jean-Marc Gilliot, Guillaume Siour, Matthias Beekmann, Gilles Foret, Frederik Meleux, Lieven Clarisse, Pierre-François Coheur, Martin Van Damme, Cathy Clerbaux, and Sophie Génermont
Atmos. Chem. Phys., 20, 13481–13495, https://doi.org/10.5194/acp-20-13481-2020, https://doi.org/10.5194/acp-20-13481-2020, 2020
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Studies have suggested the importance of ammonia emissions on pollution particle formation over Europe, whose main atmospheric source is agriculture. In this study, we performed an inter-comparison of two alternative inventories, both with a reference inventory, that quantify the French ammonia emissions during spring 2011. Over regions with large mineral fertilizer use, like over northeastern France, NH3 emissions are probably considerably underestimated by the reference inventory.
David S. Stevenson, Alcide Zhao, Vaishali Naik, Fiona M. O'Connor, Simone Tilmes, Guang Zeng, Lee T. Murray, William J. Collins, Paul T. Griffiths, Sungbo Shim, Larry W. Horowitz, Lori T. Sentman, and Louisa Emmons
Atmos. Chem. Phys., 20, 12905–12920, https://doi.org/10.5194/acp-20-12905-2020, https://doi.org/10.5194/acp-20-12905-2020, 2020
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We present historical trends in atmospheric oxidizing capacity (OC) since 1850 from the latest generation of global climate models and compare these with estimates from measurements. OC controls levels of many key reactive gases, including methane (CH4). We find small model trends up to 1980, then increases of about 9 % up to 2014, disagreeing with (uncertain) measurement-based trends. Major drivers of OC trends are emissions of CH4, NOx, and CO; these will be important for future CH4 trends.
Wenfu Tang, Benjamin Gaubert, Louisa Emmons, Yonghoon Choi, Joshua P. DiGangi, Glenn S. Diskin, Xiaomei Xu, Cenlin He, Helen Worden, Simone Tilmes, Rebecca Buchholz, Hannah S. Halliday, and Avelino F. Arellano
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2020-864, https://doi.org/10.5194/acp-2020-864, 2020
Revised manuscript not accepted
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A specific demonstration of the potential use of correlative information from carbon monoxide to refine estimates of regional carbon dioxide emissions from fossil fuel combustion.
Robert J. Allen, Steven Turnock, Pierre Nabat, David Neubauer, Ulrike Lohmann, Dirk Olivié, Naga Oshima, Martine Michou, Tongwen Wu, Jie Zhang, Toshihiko Takemura, Michael Schulz, Kostas Tsigaridis, Susanne E. Bauer, Louisa Emmons, Larry Horowitz, Vaishali Naik, Twan van Noije, Tommi Bergman, Jean-Francois Lamarque, Prodromos Zanis, Ina Tegen, Daniel M. Westervelt, Philippe Le Sager, Peter Good, Sungbo Shim, Fiona O'Connor, Dimitris Akritidis, Aristeidis K. Georgoulias, Makoto Deushi, Lori T. Sentman, Jasmin G. John, Shinichiro Fujimori, and William J. Collins
Atmos. Chem. Phys., 20, 9641–9663, https://doi.org/10.5194/acp-20-9641-2020, https://doi.org/10.5194/acp-20-9641-2020, 2020
Solène Turquety, Laurent Menut, Guillaume Siour, Sylvain Mailler, Juliette Hadji-Lazaro, Maya George, Cathy Clerbaux, Daniel Hurtmans, and Pierre-François Coheur
Geosci. Model Dev., 13, 2981–3009, https://doi.org/10.5194/gmd-13-2981-2020, https://doi.org/10.5194/gmd-13-2981-2020, 2020
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Biomass burning emissions are a major source of trace gases and aerosols that need to be accounted for in air quality assessment and forecasting. The APIFLAME model presented in this paper allows the calculation of these emissions based on merged satellite observations at hourly time steps and kilometer scales. Implementing emissions in a chemistry transport model allows realistic simulations of fire plumes as illustrated for wildfires in Portugal in August 2016 using the CHIMERE model.
Pablo E. Saide, Meng Gao, Zifeng Lu, Daniel L. Goldberg, David G. Streets, Jung-Hun Woo, Andreas Beyersdorf, Chelsea A. Corr, Kenneth L. Thornhill, Bruce Anderson, Johnathan W. Hair, Amin R. Nehrir, Glenn S. Diskin, Jose L. Jimenez, Benjamin A. Nault, Pedro Campuzano-Jost, Jack Dibb, Eric Heim, Kara D. Lamb, Joshua P. Schwarz, Anne E. Perring, Jhoon Kim, Myungje Choi, Brent Holben, Gabriele Pfister, Alma Hodzic, Gregory R. Carmichael, Louisa Emmons, and James H. Crawford
Atmos. Chem. Phys., 20, 6455–6478, https://doi.org/10.5194/acp-20-6455-2020, https://doi.org/10.5194/acp-20-6455-2020, 2020
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Air quality forecasts over the Korean Peninsula captured aerosol optical depth but largely overpredicted surface PM during a Chinese haze transport event. Model deficiency was related to the calculation of optical properties. In order to improve it, aerosol size representation needs to be refined in the calculations, and the representation of aerosol properties, such as size distribution, chemical composition, refractive index, hygroscopicity parameter, and density, needs to be improved.
Rebecca H. Schwantes, Louisa K. Emmons, John J. Orlando, Mary C. Barth, Geoffrey S. Tyndall, Samuel R. Hall, Kirk Ullmann, Jason M. St. Clair, Donald R. Blake, Armin Wisthaler, and Thao Paul V. Bui
Atmos. Chem. Phys., 20, 3739–3776, https://doi.org/10.5194/acp-20-3739-2020, https://doi.org/10.5194/acp-20-3739-2020, 2020
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Ozone is a greenhouse gas and air pollutant that is harmful to human health and plants. During the summer in the southeastern US, many regional and global models are biased high for surface ozone compared to observations. Here adding more complex and updated chemistry for isoprene and terpenes, which are biogenic hydrocarbons emitted from trees and vegetation, into an earth system model greatly reduces the simulated surface ozone bias compared to aircraft and monitoring station data.
Wenfu Tang, Helen M. Worden, Merritt N. Deeter, David P. Edwards, Louisa K. Emmons, Sara Martínez-Alonso, Benjamin Gaubert, Rebecca R. Buchholz, Glenn S. Diskin, Russell R. Dickerson, Xinrong Ren, Hao He, and Yutaka Kondo
Atmos. Meas. Tech., 13, 1337–1356, https://doi.org/10.5194/amt-13-1337-2020, https://doi.org/10.5194/amt-13-1337-2020, 2020
Wei Wang, Cheng Liu, Lieven Clarisse, Martin Van Damme, Pierre-François Coheur, Yu Xie, Changgong Shan, Qihou Hu, Huifang Zhang, Youwen Sun, Hao Yin, and Nicholas Jones
Atmos. Meas. Tech. Discuss., https://doi.org/10.5194/amt-2020-39, https://doi.org/10.5194/amt-2020-39, 2020
Revised manuscript not accepted
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Ground-based FTIR observations are used to obtain the total columns and vertical profiles of atmospheric NH3 at a measurement site in Hefei, China. The spatial distribution, temporal variation, seasonal trend, and emission sources of NH3 are analyzed. FTIR observations captured the seasonal cycle of NH3. The IASI data are in broad agreement with our FTIR data. This is the first time that ground-based FTIR remote sensing of NH3 columns and comparison with satellite data are reported in China.
Camille Viatte, Tianze Wang, Martin Van Damme, Enrico Dammers, Frederik Meleux, Lieven Clarisse, Mark W. Shephard, Simon Whitburn, Pierre François Coheur, Karen E. Cady-Pereira, and Cathy Clerbaux
Atmos. Chem. Phys., 20, 577–596, https://doi.org/10.5194/acp-20-577-2020, https://doi.org/10.5194/acp-20-577-2020, 2020
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We study concentrations and spatiotemporal variabilities of atmospheric NH3 from the agricultural sector to gain insights on its effects on the Paris megacity air quality using satellite data from IASI and CrIS.
We evaluate the regional CHIMERE model capacity to reproduce NH3 and particulate matter (PM2.5) concentrations and variabilities in the domain of study.
We quantify the main meteorological parameters driving the optimal conditions involved in the PM2.5 formation from NH3 in Paris.
Catherine Wespes, Daniel Hurtmans, Simon Chabrillat, Gaétane Ronsmans, Cathy Clerbaux, and Pierre-François Coheur
Atmos. Chem. Phys., 19, 14031–14056, https://doi.org/10.5194/acp-19-14031-2019, https://doi.org/10.5194/acp-19-14031-2019, 2019
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This paper highlights the global fingerprint of recent changes in O3 in both the middle–upper and lower stratosphere from the first 10 years of the IASI/Metop-A satellite measurements. The results present the first detection of a significant O3 recovery at middle–high latitudes in winter–spring in the stratosphere as well as in the total column from one single dataset. They also show a speeding up in the recovery at high southern latitudes contrasting with a decline at northern mid-latitudes.
Lieven Clarisse, Martin Van Damme, Cathy Clerbaux, and Pierre-François Coheur
Atmos. Meas. Tech., 12, 5457–5473, https://doi.org/10.5194/amt-12-5457-2019, https://doi.org/10.5194/amt-12-5457-2019, 2019
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An imaging technique called superresolution is applied to IASI satellite measurements of atmospheric ammonia (NH3). Taking into account wind fields, this technique reveals NH3 emission sources much better than previously possible. We present a new global NH3 point-source catalog consisting of more than 500 localized and categorized point sources related to agriculture and five different types of industry.
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.
Merritt N. Deeter, David P. Edwards, Gene L. Francis, John C. Gille, Debbie Mao, Sara Martínez-Alonso, Helen M. Worden, Dan Ziskin, and Meinrat O. Andreae
Atmos. Meas. Tech., 12, 4561–4580, https://doi.org/10.5194/amt-12-4561-2019, https://doi.org/10.5194/amt-12-4561-2019, 2019
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The MOPITT (Measurements of Pollution in the Troposphere) satellite instrument has been making nearly continuous observations of atmospheric carbon monoxide (CO) since 2000. MOPITT CO retrievals are routinely used to analyze emissions from fossil fuels and biomass burning, as well as the atmospheric transport of those emissions. This paper describes recent enhancements to the MOPITT retrieval algorithm. New validation results illustrate clear improvements in the fidelity of the MOPITT product.
Duseong S. Jo, Alma Hodzic, Louisa K. Emmons, Eloise A. Marais, Zhe Peng, Benjamin A. Nault, Weiwei Hu, Pedro Campuzano-Jost, and Jose L. Jimenez
Geosci. Model Dev., 12, 2983–3000, https://doi.org/10.5194/gmd-12-2983-2019, https://doi.org/10.5194/gmd-12-2983-2019, 2019
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We developed a parameterization method for IEPOX-SOA based on the detailed chemical mechanism. Our parameterizations were tested using a box model and 3-D chemical transport model, which accurately captured the spatiotemporal distribution and response to changes in emissions compared to the explicit full chemistry, while being more computationally efficient. The method developed in this study can be applied to global climate models for long-term studies with a lower computational cost.
Sarah Safieddine, Ana Claudia Parracho, Maya George, Filipe Aires, Victor Pellet, Lieven Clarisse, Simon Whitburn, Olivier Lezeaux, Jean-Noel Thepaut, Hans Hersbach, Gabor Radnoti, Frank Goettsche, Maria Martin, Marie Doutriaux Boucher, Dorothee Coppens, Thomas August, and Cathy Clerbaux
Atmos. Meas. Tech. Discuss., https://doi.org/10.5194/amt-2019-185, https://doi.org/10.5194/amt-2019-185, 2019
Preprint withdrawn
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Skin temperature is one of the essential climate variables (ECVs), and is relevant for the current and future understanding of our climate. This work presents a method to retrieve skin temperature from the thermal infrared sounder IASI that provides a global observation of Earth’s surface and atmosphere twice a day. With this method, the first consistent long-term [2007-present] skin temperature record from IASI can be constructed.
Mathieu Lachatre, Audrey Fortems-Cheiney, Gilles Foret, Guillaume Siour, Gaëlle Dufour, Lieven Clarisse, Cathy Clerbaux, Pierre-François Coheur, Martin Van Damme, and Matthias Beekmann
Atmos. Chem. Phys., 19, 6701–6716, https://doi.org/10.5194/acp-19-6701-2019, https://doi.org/10.5194/acp-19-6701-2019, 2019
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It has been observed from satellite-based instruments that ammonia levels strongly increased between 2011 and 2015. We have used the CHIMERE CTM to understand what could explain such an increase. We first focused on meteorological condition variations, and it has been concluded that meteorology did not explain ammonia evolution. Then, we focused on SO2 and NOx emission evolution rates to evaluate their influences on ammonia. It appears that theses decreases were the main explanation.
Kang Sun, Lei Zhu, Karen Cady-Pereira, Christopher Chan Miller, Kelly Chance, Lieven Clarisse, Pierre-François Coheur, Gonzalo González Abad, Guanyu Huang, Xiong Liu, Martin Van Damme, Kai Yang, and Mark Zondlo
Atmos. Meas. Tech., 11, 6679–6701, https://doi.org/10.5194/amt-11-6679-2018, https://doi.org/10.5194/amt-11-6679-2018, 2018
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An agile, physics-based approach is developed to oversample irregular satellite observations to a high-resolution common grid. Instead of assuming each sounding as a point or a polygon as in previous methods, the proposed physical oversampling represents soundings as distributions of sensitivity on the ground. This sensitivity distribution can be determined by the spatial response function of each satellite sensor, parameterized as generalized 2-D super Gaussian functions.
Xinyi Dong, Joshua S. Fu, Qingzhao Zhu, Jian Sun, Jiani Tan, Terry Keating, Takashi Sekiya, Kengo Sudo, Louisa Emmons, Simone Tilmes, Jan Eiof Jonson, Michael Schulz, Huisheng Bian, Mian Chin, Yanko Davila, Daven Henze, Toshihiko Takemura, Anna Maria Katarina Benedictow, and Kan Huang
Atmos. Chem. Phys., 18, 15581–15600, https://doi.org/10.5194/acp-18-15581-2018, https://doi.org/10.5194/acp-18-15581-2018, 2018
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We have applied the HTAP phase II multi-model data to investigate the long-range transport impacts on surface concentration and column density of PM from Europe and Russia, Belarus, and Ukraine to eastern Asia, with a special focus on the long-range transport contribution during haze episodes in China. We found that long-range transport plays a more important role in elevating the background concentration of surface PM during the haze days.
Benjamin Brown-Steiner, Noelle E. Selin, Ronald Prinn, Simone Tilmes, Louisa Emmons, Jean-François Lamarque, and Philip Cameron-Smith
Geosci. Model Dev., 11, 4155–4174, https://doi.org/10.5194/gmd-11-4155-2018, https://doi.org/10.5194/gmd-11-4155-2018, 2018
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We conduct three simulations of atmospheric chemistry using chemical mechanisms of different levels of complexity and compare their results to observations. We explore situations in which the simplified mechanisms match the output of the most complex mechanism, as well as when they diverge. We investigate how concurrent utilization of chemical mechanisms of different complexities can further our atmospheric-chemistry understanding at various scales and give some strategies for future research.
Jan Eiof Jonson, Michael Schulz, Louisa Emmons, Johannes Flemming, Daven Henze, Kengo Sudo, Marianne Tronstad Lund, Meiyun Lin, Anna Benedictow, Brigitte Koffi, Frank Dentener, Terry Keating, Rigel Kivi, and Yanko Davila
Atmos. Chem. Phys., 18, 13655–13672, https://doi.org/10.5194/acp-18-13655-2018, https://doi.org/10.5194/acp-18-13655-2018, 2018
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Focusing on Europe, this HTAP 2 study computes ozone in several global models when reducing anthropogenic emissions by 20 % in different world regions. The differences in model results are explored
by use of a novel stepwise approach combining a tracer, CO and ozone. For ozone the contributions from the rest of the world are larger than from Europe, with the largest contributions from North America and eastern Asia. Contributions do, however, depend on the choice of ozone metric.
Arthur P. Mizzi, David P. Edwards, and Jeffrey L. Anderson
Geosci. Model Dev., 11, 3727–3745, https://doi.org/10.5194/gmd-11-3727-2018, https://doi.org/10.5194/gmd-11-3727-2018, 2018
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Accurate air quality forecasts are critical to protecting human health and the environment. This paper shows how ensemble assimilation of MOPITT CO
compact phase space retrieval(CPSR) profiles in WRF-Chem/DART provides significant improvements in the air quality forecasts over the CONUS when compared to independent remote (IASI CO retrieval profiles) and in situ (IAGOS/MOZAIC) observations. It also extends the CPSR algorithm to assimilation of truncated retrieval profiles.
Anne Boynard, Daniel Hurtmans, Katerina Garane, Florence Goutail, Juliette Hadji-Lazaro, Maria Elissavet Koukouli, Catherine Wespes, Corinne Vigouroux, Arno Keppens, Jean-Pierre Pommereau, Andrea Pazmino, Dimitris Balis, Diego Loyola, Pieter Valks, Ralf Sussmann, Dan Smale, Pierre-François Coheur, and Cathy Clerbaux
Atmos. Meas. Tech., 11, 5125–5152, https://doi.org/10.5194/amt-11-5125-2018, https://doi.org/10.5194/amt-11-5125-2018, 2018
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In this paper, we perform a comprehensive validation of the IASI/Metop ozone data using independent observations (satellite, ground-based and ozonesonde). The quality of the IASI total and tropospheric ozone columns in terms of bias and long-term stability is generally good. Compared with ozonesonde data, IASI overestimates (underestimates) the ozone abundance in the stratosphere (troposphere). A negative drift in tropospheric ozone is observed, which is not well understood at this point.
Jiali Luo, Laura L. Pan, Shawn B. Honomichl, John W. Bergman, William J. Randel, Gene Francis, Cathy Clerbaux, Maya George, Xiong Liu, and Wenshou Tian
Atmos. Chem. Phys., 18, 12511–12530, https://doi.org/10.5194/acp-18-12511-2018, https://doi.org/10.5194/acp-18-12511-2018, 2018
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We analyze upper tropospheric CO and O3 using satellite data from limb-viewing (MLS) and nadir-viewing (IASI and OMI) sensors, together with dynamical variables, to examine how the two types of data complement each other in representing the chemical variability associated with the day-to-day dynamical variability in the Asian summer monsoon anticyclone. The results provide new observational evidence of eddy shedding in upper tropospheric CO distribution.
Jiani Tan, Joshua S. Fu, Frank Dentener, Jian Sun, Louisa Emmons, Simone Tilmes, Johannes Flemming, Toshihiko Takemura, Huisheng Bian, Qingzhao Zhu, Cheng-En Yang, and Terry Keating
Atmos. Chem. Phys., 18, 12223–12240, https://doi.org/10.5194/acp-18-12223-2018, https://doi.org/10.5194/acp-18-12223-2018, 2018
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Have contributions of hemispheric air pollution to deposition at global scale been overlooked in the past years? How do we assess the critical load for the acid deposition when we look for the demand of forest and crop? This study highlights the significant impact of hemispheric transport on deposition in coastal regions, open ocean and low-emission regions. Further research is proposed for improving ecosystem and human health in these regions, with regards to the enhanced hemispheric transport.
Ciao-Kai Liang, J. Jason West, Raquel A. Silva, Huisheng Bian, Mian Chin, Yanko Davila, Frank J. Dentener, Louisa Emmons, Johannes Flemming, Gerd Folberth, Daven Henze, Ulas Im, Jan Eiof Jonson, Terry J. Keating, Tom Kucsera, Allen Lenzen, Meiyun Lin, Marianne Tronstad Lund, Xiaohua Pan, Rokjin J. Park, R. Bradley Pierce, Takashi Sekiya, Kengo Sudo, and Toshihiko Takemura
Atmos. Chem. Phys., 18, 10497–10520, https://doi.org/10.5194/acp-18-10497-2018, https://doi.org/10.5194/acp-18-10497-2018, 2018
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Emissions from one continent affect air quality and health elsewhere. Here we quantify the effects of intercontinental PM2.5 and ozone transport on human health using a new multi-model ensemble, evaluating the health effects of emissions from six world regions and three emission source sectors. Emissions from one region have significant health impacts outside of that source region; similarly, foreign emissions contribute significantly to air-pollution-related deaths in several world regions.
Steven T. Turnock, Oliver Wild, Frank J. Dentener, Yanko Davila, Louisa K. Emmons, Johannes Flemming, Gerd A. Folberth, Daven K. Henze, Jan E. Jonson, Terry J. Keating, Sudo Kengo, Meiyun Lin, Marianne Lund, Simone Tilmes, and Fiona M. O'Connor
Atmos. Chem. Phys., 18, 8953–8978, https://doi.org/10.5194/acp-18-8953-2018, https://doi.org/10.5194/acp-18-8953-2018, 2018
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A simple parameterisation was developed in this study to provide a rapid assessment of the impacts and uncertainties associated with future emission control strategies by predicting changes to surface ozone air quality and near-term climate forcing of ozone. Future emissions scenarios based on currently implemented legislation are shown to worsen surface ozone air quality and enhance near-term climate warming, with changes in methane becoming increasingly important in the future.
Arno Keppens, Jean-Christopher Lambert, José Granville, Daan Hubert, Tijl Verhoelst, Steven Compernolle, Barry Latter, Brian Kerridge, Richard Siddans, Anne Boynard, Juliette Hadji-Lazaro, Cathy Clerbaux, Catherine Wespes, Daniel R. Hurtmans, Pierre-François Coheur, Jacob C. A. van Peet, Ronald J van der A, Katerina Garane, Maria Elissavet Koukouli, Dimitris S. Balis, Andy Delcloo, Rigel Kivi, Réné Stübi, Sophie Godin-Beekmann, Michel Van Roozendael, and Claus Zehner
Atmos. Meas. Tech., 11, 3769–3800, https://doi.org/10.5194/amt-11-3769-2018, https://doi.org/10.5194/amt-11-3769-2018, 2018
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This work, performed at the Royal Belgian Institute for Space Aeronomy and the second in a series of four Ozone_cci papers, reports for the first time on data content studies, information content studies, and comparisons with co-located ground-based reference observations for all 13 nadir ozone profile data products that are part of the Climate Research Data Package (CRDP) on atmospheric ozone of the European Space Agency's Climate Change Initiative.
Benjamin Brown-Steiner, Noelle E. Selin, Ronald G. Prinn, Erwan Monier, Simone Tilmes, Louisa Emmons, and Fernando Garcia-Menendez
Atmos. Chem. Phys., 18, 8373–8388, https://doi.org/10.5194/acp-18-8373-2018, https://doi.org/10.5194/acp-18-8373-2018, 2018
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Detecting signals in observations and simulations of atmospheric chemistry is difficult due to the underlying variability in the chemistry, meteorology, and climatology. Here we examine the scale dependence of ozone variability and explore strategies for reducing or averaging this variability and thereby enhancing ozone signal detection capabilities. We find that 10–15 years of temporal averaging, and some level of spatial averaging, reduces the risk of overconfidence in ozone signals.
Catherine Wespes, Daniel Hurtmans, Cathy Clerbaux, Anne Boynard, and Pierre-François Coheur
Atmos. Chem. Phys., 18, 6867–6885, https://doi.org/10.5194/acp-18-6867-2018, https://doi.org/10.5194/acp-18-6867-2018, 2018
Jiani Tan, Joshua S. Fu, Frank Dentener, Jian Sun, Louisa Emmons, Simone Tilmes, Kengo Sudo, Johannes Flemming, Jan Eiof Jonson, Sylvie Gravel, Huisheng Bian, Yanko Davila, Daven K. Henze, Marianne T. Lund, Tom Kucsera, Toshihiko Takemura, and Terry Keating
Atmos. Chem. Phys., 18, 6847–6866, https://doi.org/10.5194/acp-18-6847-2018, https://doi.org/10.5194/acp-18-6847-2018, 2018
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We study the distributions of sulfur and nitrogen deposition, which are associated with current environmental issues such as formation of acid rain and ecosystem eutrophication and result in widespread problems such as loss of environmental diversity, harming the crop yield and even food insecurity. According to our study, both the amount and distribution of sulfate and nitrogen deposition have changed significantly in the last decade, particularly in East Asia, South Asia and Southeast Asia.
Martin G. Schultz, Scarlet Stadtler, Sabine Schröder, Domenico Taraborrelli, Bruno Franco, Jonathan Krefting, Alexandra Henrot, Sylvaine Ferrachat, Ulrike Lohmann, David Neubauer, Colombe Siegenthaler-Le Drian, Sebastian Wahl, Harri Kokkola, Thomas Kühn, Sebastian Rast, Hauke Schmidt, Philip Stier, Doug Kinnison, Geoffrey S. Tyndall, John J. Orlando, and Catherine Wespes
Geosci. Model Dev., 11, 1695–1723, https://doi.org/10.5194/gmd-11-1695-2018, https://doi.org/10.5194/gmd-11-1695-2018, 2018
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The chemistry–climate model ECHAM-HAMMOZ contains a detailed representation of tropospheric and stratospheric reactive chemistry and state-of-the-art parameterizations of aerosols. It thus allows for detailed investigations of chemical processes in the climate system. Evaluation of the model with various observational data yields good results, but the model has a tendency to produce too much OH in the tropics. This highlights the important interplay between atmospheric chemistry and dynamics.
Gaétane Ronsmans, Catherine Wespes, Daniel Hurtmans, Cathy Clerbaux, and Pierre-François Coheur
Atmos. Chem. Phys., 18, 4403–4423, https://doi.org/10.5194/acp-18-4403-2018, https://doi.org/10.5194/acp-18-4403-2018, 2018
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The paper aims at understanding the variability of nitric acid (HNO3) in the stratosphere; 9-year time series of IASI measurements are analysed and, for the first time for HNO3, fitted with regression models in order to identify the factors at play. It was found that the annual variability is the main driver and that the polar stratospheric clouds influence greatly HNO3 variability at polar latitudes. The results show the potential of such analyses to better understand the polar processes.
David P. Edwards, Helen M. Worden, Doreen Neil, Gene Francis, Tim Valle, and Avelino F. Arellano Jr.
Atmos. Meas. Tech., 11, 1061–1085, https://doi.org/10.5194/amt-11-1061-2018, https://doi.org/10.5194/amt-11-1061-2018, 2018
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The CHRONOS space mission would provide observations for emissions and transport studies of the highly uncertain air pollutants carbon monoxide and methane, with sub-hourly revisit at fine horizontal spatial resolution across North America. CHRONOS uses an imaging gas filter correlation radiometer hosted in geostationary orbit. CHRONOS' capability for monitoring evolving, or unanticipated, air pollution sources would find societal applications for air quality management and forecasting.
Martin Van Damme, Simon Whitburn, Lieven Clarisse, Cathy Clerbaux, Daniel Hurtmans, and Pierre-François Coheur
Atmos. Meas. Tech., 10, 4905–4914, https://doi.org/10.5194/amt-10-4905-2017, https://doi.org/10.5194/amt-10-4905-2017, 2017
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This paper presents an improved version (v2.1) of the neural-network-based algorithm for retrieving atmospheric ammonia (NH3) columns from IASI satellite observations. Two datasets using different input data for the retrieval are described: one is based on the operationally provided EUMETSAT Level 2 (ANNI-NH3-v2.1), and the other uses the ECMWF ERA-Interim data (ANNI-NH3-v2.1R-I). Analyses illustrate well that the (meteorological) input data can have a large impact on the retrieved NH3 columns.
Simon Whitburn, Martin Van Damme, Lieven Clarisse, Daniel Hurtmans, Cathy Clerbaux, and Pierre-François Coheur
Atmos. Chem. Phys., 17, 12239–12252, https://doi.org/10.5194/acp-17-12239-2017, https://doi.org/10.5194/acp-17-12239-2017, 2017
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Vegetation fires are a major source of NH3 in the atmosphere. A key parameter for the calculation of their emissions, which are still uncertain, is the NH3 enhancement ratio relative to carbon monoxide (CO), ERNH3 / CO. Here we derive new ERNH3 / CO ratios for large tropical regions from the measurements of IASI. We find important variability between and within the studied biomes, as well as interannual variability. This highlights the need for the development of dynamic ERNH3 / CO ratios.
Matthieu Pommier, Cathy Clerbaux, and Pierre-Francois Coheur
Atmos. Chem. Phys., 17, 11089–11105, https://doi.org/10.5194/acp-17-11089-2017, https://doi.org/10.5194/acp-17-11089-2017, 2017
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A new estimation of enhancement ratios relative to CO for HCOOH over seven biomass burning regions is proposed. Fire-affected HCOOH and CO total columns are defined by combining the total columns from IASI, geographic location of the fires from the Moderate Resolution Imaging Spectroradiometer (MODIS), and surface wind speed field from the European Centre for Medium-Range Weather Forecasts (ECMWF). An additional classification of the enhancement ratios by type of fuel burned is also provided.
Valentin Duflot, Jean-Luc Baray, Guillaume Payen, Nicolas Marquestaut, Francoise Posny, Jean-Marc Metzger, Bavo Langerock, Corinne Vigouroux, Juliette Hadji-Lazaro, Thierry Portafaix, Martine De Mazière, Pierre-Francois Coheur, Cathy Clerbaux, and Jean-Pierre Cammas
Atmos. Meas. Tech., 10, 3359–3373, https://doi.org/10.5194/amt-10-3359-2017, https://doi.org/10.5194/amt-10-3359-2017, 2017
Jihyun Han, Meehye Lee, Xiaona Shang, Gangwoong Lee, and Louisa K. Emmons
Atmos. Chem. Phys., 17, 10619–10631, https://doi.org/10.5194/acp-17-10619-2017, https://doi.org/10.5194/acp-17-10619-2017, 2017
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Peroxyacetyl nitrate (PAN) was first measured at Gosan Climate Observatory during the fall of 2010, when PAN was better correlated with PM10 than with O3. In particular, PAN and O3 concentrations were greatly elevated in haze and the Beijing plume and much higher than those from model simulation. This study highlights the decoupling of PAN from O3 in Chinese outflows and suggests PAN as a potential indicator of overall aerosol formation in aged air masses impacted by biomass burning.
Jean-Lionel Lacour, Cyrille Flamant, Camille Risi, Cathy Clerbaux, and Pierre-François Coheur
Atmos. Chem. Phys., 17, 9645–9663, https://doi.org/10.5194/acp-17-9645-2017, https://doi.org/10.5194/acp-17-9645-2017, 2017
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We present temporal and spatial δD distributions derived from IASI obtained above the North Atlantic in the vicinity of West Africa. We show that the seasonality of δD in the North Atlantic is closely associated with the influence of the Saharan heat low (SHL). We provide an interpretation of the temporal and spatial variations in δD and show that the interactions between the large-scale subsidence, the ITCZ, and the SHL can be disentangled thanks to the added information contained in δD.
Merritt N. Deeter, David P. Edwards, Gene L. Francis, John C. Gille, Sara Martínez-Alonso, Helen M. Worden, and Colm Sweeney
Atmos. Meas. Tech., 10, 2533–2555, https://doi.org/10.5194/amt-10-2533-2017, https://doi.org/10.5194/amt-10-2533-2017, 2017
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This manuscript describes the methods used for deriving the latest version 7 product for atmospheric carbon monoxide (CO) from measurements made by the MOPITT (Measurements of Pollution in the Troposphere) satellite instrument. Comparisons of MOPITT-retrieved CO vertical profiles with in situ data measured from aircraft are also presented, and they demonstrate clear improvements relative to earlier MOPITT products. The new CO product is appropriate for a wide variety of applications.
Rebecca R. Buchholz, Merritt N. Deeter, Helen M. Worden, John Gille, David P. Edwards, James W. Hannigan, Nicholas B. Jones, Clare Paton-Walsh, David W. T. Griffith, Dan Smale, John Robinson, Kimberly Strong, Stephanie Conway, Ralf Sussmann, Frank Hase, Thomas Blumenstock, Emmanuel Mahieu, and Bavo Langerock
Atmos. Meas. Tech., 10, 1927–1956, https://doi.org/10.5194/amt-10-1927-2017, https://doi.org/10.5194/amt-10-1927-2017, 2017
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The study presents the first systematic use of ground-based remote-sensing data from the Network for the Detection of Atmospheric Composition Change (NDACC) to validate satellite-based Measurements of Pollution in the Troposphere (MOPITT) total column carbon monoxide (CO). MOPITT generally shows low bias with respect to the ground-based instruments. The geographic and temporal dependence of validation results are determined. Our findings inform some recommendations for using MOPITT measurements.
Yi Li, Tammy M. Thompson, Martin Van Damme, Xi Chen, Katherine B. Benedict, Yixing Shao, Derek Day, Alexandra Boris, Amy P. Sullivan, Jay Ham, Simon Whitburn, Lieven Clarisse, Pierre-François Coheur, and Jeffrey L. Collett Jr.
Atmos. Chem. Phys., 17, 6197–6213, https://doi.org/10.5194/acp-17-6197-2017, https://doi.org/10.5194/acp-17-6197-2017, 2017
Min Huang, Gregory R. Carmichael, R. Bradley Pierce, Duseong S. Jo, Rokjin J. Park, Johannes Flemming, Louisa K. Emmons, Kevin W. Bowman, Daven K. Henze, Yanko Davila, Kengo Sudo, Jan Eiof Jonson, Marianne Tronstad Lund, Greet Janssens-Maenhout, Frank J. Dentener, Terry J. Keating, Hilke Oetjen, and Vivienne H. Payne
Atmos. Chem. Phys., 17, 5721–5750, https://doi.org/10.5194/acp-17-5721-2017, https://doi.org/10.5194/acp-17-5721-2017, 2017
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In support of the HTAP phase 2 experiment, we conducted a number of regional-scale Sulfur Transport and dEposition Model base and sensitivity simulations over North America during May–June 2010. The STEM chemical boundary conditions were downscaled from three (GEOS-Chem, RAQMS, and ECMWF C-IFS) global chemical transport models' simulations. Analyses were performed on large spatial–temporal scales relative to HTAP1 and also on subcontinental and event scales including the use of satellite data.
Camilla Weum Stjern, Bjørn Hallvard Samset, Gunnar Myhre, Huisheng Bian, Mian Chin, Yanko Davila, Frank Dentener, Louisa Emmons, Johannes Flemming, Amund Søvde Haslerud, Daven Henze, Jan Eiof Jonson, Tom Kucsera, Marianne Tronstad Lund, Michael Schulz, Kengo Sudo, Toshihiko Takemura, and Simone Tilmes
Atmos. Chem. Phys., 16, 13579–13599, https://doi.org/10.5194/acp-16-13579-2016, https://doi.org/10.5194/acp-16-13579-2016, 2016
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Air pollution can reach distant regions through intercontinental transport. Here we first present results from the Hemispheric Transport of Air Pollution Phase 2 exercise, where many models performed the same set of coordinated emission-reduction experiments. We find that mitigations have considerable extra-regional effects, and show that this is particularly true for black carbon emissions, as long-range transport elevates aerosols to higher levels where their radiative influence is stronger.
Luke D. Schiferl, Colette L. Heald, Martin Van Damme, Lieven Clarisse, Cathy Clerbaux, Pierre-François Coheur, John B. Nowak, J. Andrew Neuman, Scott C. Herndon, Joseph R. Roscioli, and Scott J. Eilerman
Atmos. Chem. Phys., 16, 12305–12328, https://doi.org/10.5194/acp-16-12305-2016, https://doi.org/10.5194/acp-16-12305-2016, 2016
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This study combines new observations and a simulation to assess the interannual variability of atmospheric ammonia concentrations over the United States. The model generally underrepresents the observed variability. Nearly two-thirds of the simulated variability is caused by meteorology, twice that caused by regulations on fossil fuel combustion emissions. Adding ammonia emissions variability does not substantially improve the simulation and has little impact on summer particle concentrations.
Gaétane Ronsmans, Bavo Langerock, Catherine Wespes, James W. Hannigan, Frank Hase, Tobias Kerzenmacher, Emmanuel Mahieu, Matthias Schneider, Dan Smale, Daniel Hurtmans, Martine De Mazière, Cathy Clerbaux, and Pierre-François Coheur
Atmos. Meas. Tech., 9, 4783–4801, https://doi.org/10.5194/amt-9-4783-2016, https://doi.org/10.5194/amt-9-4783-2016, 2016
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HNO3 concentrations are obtained from the IASI instrument and the data set is characterized for the first time in terms of vertical profiles, averaging kernels and error profiles. A validation is also conducted through a comparison with ground-based FTIR measurements, with good results. The data set is then used to analyse HNO3 spatial and temporal variability for the year 2011. The latitudinal gradient and the large seasonal variability in polar regions are well represented with IASI data.
Anne Boynard, Daniel Hurtmans, Mariliza E. Koukouli, Florence Goutail, Jérôme Bureau, Sarah Safieddine, Christophe Lerot, Juliette Hadji-Lazaro, Catherine Wespes, Jean-Pierre Pommereau, Andrea Pazmino, Irene Zyrichidou, Dimitris Balis, Alain Barbe, Semen N. Mikhailenko, Diego Loyola, Pieter Valks, Michel Van Roozendael, Pierre-François Coheur, and Cathy Clerbaux
Atmos. Meas. Tech., 9, 4327–4353, https://doi.org/10.5194/amt-9-4327-2016, https://doi.org/10.5194/amt-9-4327-2016, 2016
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Seven years of O3 observations retrieved from IASI/MetOp satellite instruments are validated with independent data (UV satellite and ground-based data along with ozonesonde profiles). Overall IASI overestimates the total ozone columns (TOC) by 2–7 % depending on the latitude. The assessment of an updated version of the IASI O3 retrieval sofware shows a correction of ~ 4 % in the IASI TOC product, bringing the overall global bias with UV ground-based and satellite data to ~ 1–2 % on average.
Yao Té, Pascal Jeseck, Bruno Franco, Emmanuel Mahieu, Nicholas Jones, Clare Paton-Walsh, David W. T. Griffith, Rebecca R. Buchholz, Juliette Hadji-Lazaro, Daniel Hurtmans, and Christof Janssen
Atmos. Chem. Phys., 16, 10911–10925, https://doi.org/10.5194/acp-16-10911-2016, https://doi.org/10.5194/acp-16-10911-2016, 2016
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This paper studies the seasonal variation of surface and column CO at three different sites (Paris, Jungfraujoch and Wollongong), with an emphasis on establishing a link between the CO vertical distribution and the nature of CO emission sources. We find the first evidence of a time lag between surface and free tropospheric CO seasonal variations in the Northern Hemisphere.
B. Quennehen, J.-C. Raut, K. S. Law, N. Daskalakis, G. Ancellet, C. Clerbaux, S.-W. Kim, M. T. Lund, G. Myhre, D. J. L. Olivié, S. Safieddine, R. B. Skeie, J. L. Thomas, S. Tsyro, A. Bazureau, N. Bellouin, M. Hu, M. Kanakidou, Z. Klimont, K. Kupiainen, S. Myriokefalitakis, J. Quaas, S. T. Rumbold, M. Schulz, R. Cherian, A. Shimizu, J. Wang, S.-C. Yoon, and T. Zhu
Atmos. Chem. Phys., 16, 10765–10792, https://doi.org/10.5194/acp-16-10765-2016, https://doi.org/10.5194/acp-16-10765-2016, 2016
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This paper evaluates the ability of six global models and one regional model in reproducing short-lived pollutants (defined here as ozone and its precursors, aerosols and black carbon) concentrations over Asia using satellite, ground-based and airborne observations.
Key findings are that models homogeneously reproduce the trace gas observations although nitrous oxides are underestimated, whereas the aerosol distributions are heterogeneously reproduced, implicating important uncertainties.
Sarah Safieddine, Anne Boynard, Nan Hao, Fuxiang Huang, Lili Wang, Dongsheng Ji, Brice Barret, Sachin D. Ghude, Pierre-François Coheur, Daniel Hurtmans, and Cathy Clerbaux
Atmos. Chem. Phys., 16, 10489–10500, https://doi.org/10.5194/acp-16-10489-2016, https://doi.org/10.5194/acp-16-10489-2016, 2016
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The Asian Summer Monsoon has implication on the weather and climate system as well as pollutants concentration over the monsoon regions leading to effects on the global air quality. Our results, combining satellite, aircraft and ground station data, show that tropospheric ozone, decrease during the period May–August over East and South Asia due to the Monsoon. The magnitude of this drop depends largely on meteorology and geographic location.
Enrico Dammers, Mathias Palm, Martin Van Damme, Corinne Vigouroux, Dan Smale, Stephanie Conway, Geoffrey C. Toon, Nicholas Jones, Eric Nussbaumer, Thorsten Warneke, Christof Petri, Lieven Clarisse, Cathy Clerbaux, Christian Hermans, Erik Lutsch, Kim Strong, James W. Hannigan, Hideaki Nakajima, Isamu Morino, Beatriz Herrera, Wolfgang Stremme, Michel Grutter, Martijn Schaap, Roy J. Wichink Kruit, Justus Notholt, Pierre-F. Coheur, and Jan Willem Erisman
Atmos. Chem. Phys., 16, 10351–10368, https://doi.org/10.5194/acp-16-10351-2016, https://doi.org/10.5194/acp-16-10351-2016, 2016
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Atmospheric ammonia (NH3) measured by the IASI satellite instrument is compared to observations from ground-based FTIR instruments. The seasonal cycles of NH3 in both datasets are consistent for most sites. Correlations are found to be high at sites with considerable NH3 levels, whereas correlations are lower at sites with low NH3 levels close to the detection limit of the IASI instrument. The study's results further indicate that the IASI-NH3 product performs better than earlier estimates.
Hilke Oetjen, Vivienne H. Payne, Jessica L. Neu, Susan S. Kulawik, David P. Edwards, Annmarie Eldering, Helen M. Worden, and John R. Worden
Atmos. Chem. Phys., 16, 10229–10239, https://doi.org/10.5194/acp-16-10229-2016, https://doi.org/10.5194/acp-16-10229-2016, 2016
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We developed and tested a strategy for combining TES and IASI free-tropospheric ozone data. A time series of the merged ozone data is presented for regional monthly means over the western US, Europe, and eastern Asia. We show that free-tropospheric ozone over Europe and the western US has remained relatively constant over the past decade but that, contrary to expectations, ozone over Asia in recent years does not continue the rapid rate of increase observed from 2004–2010.
Matthieu Pommier, Cathy Clerbaux, Pierre-François Coheur, Emmanuel Mahieu, Jean-François Müller, Clare Paton-Walsh, Trissevgeni Stavrakou, and Corinne Vigouroux
Atmos. Chem. Phys., 16, 8963–8981, https://doi.org/10.5194/acp-16-8963-2016, https://doi.org/10.5194/acp-16-8963-2016, 2016
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This work presents for the first time 7 years of formic acid (HCOOH) measurements recorded by the satellite instrument, IASI. The comparison of the data set with ground-based FTIR measurements and a CTM shows the interannual and the seasonal variation are well captured. Global distributions are provided, highlighting the long-range transport of tropospheric HCOOH over the oceans and the detection of source regions e.g. over India, USA, and Africa.
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.
Simone Tilmes, Jean-Francois Lamarque, Louisa K. Emmons, Doug E. Kinnison, Dan Marsh, Rolando R. Garcia, Anne K. Smith, Ryan R. Neely, Andrew Conley, Francis Vitt, Maria Val Martin, Hiroshi Tanimoto, Isobel Simpson, Don R. Blake, and Nicola Blake
Geosci. Model Dev., 9, 1853–1890, https://doi.org/10.5194/gmd-9-1853-2016, https://doi.org/10.5194/gmd-9-1853-2016, 2016
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The state of the art Community Earth System Model, CESM1 CAM4-chem has been used to perform reference and sensitivity simulations as part of the Chemistry Climate Model Initiative (CCMI). Specifics of the model and details regarding the setup of the simulations are described. In additions, the main behavior of the model, including selected chemical species have been evaluated with climatological datasets. This paper is therefore a references for studies that use the provided model results.
Arthur P. Mizzi, Avelino F. Arellano Jr., David P. Edwards, Jeffrey L. Anderson, and Gabriele G. Pfister
Geosci. Model Dev., 9, 965–978, https://doi.org/10.5194/gmd-9-965-2016, https://doi.org/10.5194/gmd-9-965-2016, 2016
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This paper introduces (i) WRF-Chem/DART – a state-of-the-art chemical transport/data assimilation system, and (ii) compact phase space retrievals (CPSRs). WRF-Chem/DART is NCAR's regional chemical weather forecasting prototype. Such systems require assimilation of chemical composition observations, such as trace gas retrievals. Retrievals are expensive to assimilate. CPSRs reduce those assimilation costs (~ 35 % for MOPITT CO) without loss in forecast skill by removing redundant information.
Sophie Bauduin, Lieven Clarisse, Juliette Hadji-Lazaro, Nicolas Theys, Cathy Clerbaux, and Pierre-François Coheur
Atmos. Meas. Tech., 9, 721–740, https://doi.org/10.5194/amt-9-721-2016, https://doi.org/10.5194/amt-9-721-2016, 2016
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The paper presents the development of a new retrieval scheme to infer near-surface sulfur dioxide (SO2) concentrations at a global scale from the Infrared Atmospheric Sounding Interferometer (IASI). It demonstrates the capability of such an instrument to globally monitor anthropogenic SO2 pollution in the case of favourable geophysical conditions, especially high thermal contrast and low humidity.
A. Wagner, A.-M. Blechschmidt, I. Bouarar, E.-G. Brunke, C. Clerbaux, M. Cupeiro, P. Cristofanelli, H. Eskes, J. Flemming, H. Flentje, M. George, S. Gilge, A. Hilboll, A. Inness, J. Kapsomenakis, A. Richter, L. Ries, W. Spangl, O. Stein, R. Weller, and C. Zerefos
Atmos. Chem. Phys., 15, 14005–14030, https://doi.org/10.5194/acp-15-14005-2015, https://doi.org/10.5194/acp-15-14005-2015, 2015
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The Monitoring Atmospheric Composition and Climate project (MACC) operationally produces global analyses and forecasts of reactive gases and aerosol fields. We have investigated the ability of the model to simulate concentrations of reactive gases (carbon monoxide, nitrogen dioxide and ozone) between 2009 and 2012. The model reproduced reactive gas concentrations with consistent quality, however, with a seasonally dependent bias compared to surface and satellite observations.
J. He, Y. Zhang, S. Tilmes, L. Emmons, J.-F. Lamarque, T. Glotfelty, A. Hodzic, and F. Vitt
Geosci. Model Dev., 8, 3999–4025, https://doi.org/10.5194/gmd-8-3999-2015, https://doi.org/10.5194/gmd-8-3999-2015, 2015
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The global simulations with CB05_GE and MOZART-4x predict similar chemical profiles for major gases compared to aircraft measurements, with better agreement for the NOy profile by CB05_GE. The SOA concentrations of SOA at four sites in CONUS and organic carbon over the IMPROVE sites are better predicted by MOZART-4x. The two simulations result in a global average difference of 0.5W m-2 in simulated shortwave cloud radiative forcing, with up to 13.6W m-2 over subtropical regions.
Y. Zheng, N. Unger, A. Hodzic, L. Emmons, C. Knote, S. Tilmes, J.-F. Lamarque, and P. Yu
Atmos. Chem. Phys., 15, 13487–13506, https://doi.org/10.5194/acp-15-13487-2015, https://doi.org/10.5194/acp-15-13487-2015, 2015
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Nitrogen oxides (NOx) play an important but complex role in secondary organic aerosol (SOA) formation. In this study we update the SOA scheme in a global 3-D chemistry-climate model by implementing a 4-product volatility basis set (VBS) framework with NOx-dependent yields and simplified aging parameterizations. We find that the SOA decrease in response to a 50% reduction in anthropogenic NOx emissions is limited due to the buffering in different chemical pathways.
S. Doniki, D. Hurtmans, L. Clarisse, C. Clerbaux, H. M. Worden, K. W. Bowman, and P.-F. Coheur
Atmos. Chem. Phys., 15, 12971–12987, https://doi.org/10.5194/acp-15-12971-2015, https://doi.org/10.5194/acp-15-12971-2015, 2015
T. Stavrakou, J.-F. Müller, M. Bauwens, I. De Smedt, M. Van Roozendael, M. De Mazière, C. Vigouroux, F. Hendrick, M. George, C. Clerbaux, P.-F. Coheur, and A. Guenther
Atmos. Chem. Phys., 15, 11861–11884, https://doi.org/10.5194/acp-15-11861-2015, https://doi.org/10.5194/acp-15-11861-2015, 2015
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Formaldehyde columns from two space sensors, GOME-2 and OMI, constrain by inverse modeling the global emissions of HCHO precursors in 2010. The resulting biogenic and pyrogenic fluxes from both optimizations show a very good degree of consistency. The isoprene fluxes are reduced globally by ca. 10%, and emissions from fires decrease by ca. 35%, compared to the prior. Anthropogenic emissions are weakly constrained except over China. Sensitivity inversions show robustness of the inferred fluxes.
M. George, C. Clerbaux, I. Bouarar, P.-F. Coheur, M. N. Deeter, D. P. Edwards, G. Francis, J. C. Gille, J. Hadji-Lazaro, D. Hurtmans, A. Inness, D. Mao, and H. M. Worden
Atmos. Meas. Tech., 8, 4313–4328, https://doi.org/10.5194/amt-8-4313-2015, https://doi.org/10.5194/amt-8-4313-2015, 2015
V. Duflot, C. Wespes, L. Clarisse, D. Hurtmans, Y. Ngadi, N. Jones, C. Paton-Walsh, J. Hadji-Lazaro, C. Vigouroux, M. De Mazière, J.-M. Metzger, E. Mahieu, C. Servais, F. Hase, M. Schneider, C. Clerbaux, and P.-F. Coheur
Atmos. Chem. Phys., 15, 10509–10527, https://doi.org/10.5194/acp-15-10509-2015, https://doi.org/10.5194/acp-15-10509-2015, 2015
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We present global distributions of acetylene (C2H2) and hydrogen cyanide (HCN) total
columns derived from the Infrared Atmospheric Sounding Interferometer (IASI). C2H2 and HCN are ubiquitous atmospheric trace gases with medium tropospheric lifetime, which are frequently used as indicators of combustion sources and as tracers for atmospheric transport and chemistry. We show that there is an overall agreement between ground-based and space measurements, as well as model simulations.
G. Baldassarre, L. Pozzoli, C. C. Schmidt, A. Unal, T. Kindap, W. P. Menzel, S. Whitburn, P.-F. Coheur, A. Kavgaci, and J. W. Kaiser
Atmos. Chem. Phys., 15, 8539–8558, https://doi.org/10.5194/acp-15-8539-2015, https://doi.org/10.5194/acp-15-8539-2015, 2015
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We investigate the quality of fire emission estimates derived from SEVIRI FRP for air quality simulations with the Community Multiscale Air Quality (CMAQ) model, by comparing them with available MODIS FRP-based ones.
We demonstrate that geostationary observations allow for refining biomass burning emissions, which can subsequently be used in regional scale air quality models in order to improve the prediction of chemical composition of the atmosphere in presence of large fire episodes.
M. Boichu, L. Clarisse, J.-C. Péré, H. Herbin, P. Goloub, F. Thieuleux, F. Ducos, C. Clerbaux, and D. Tanré
Atmos. Chem. Phys., 15, 8381–8400, https://doi.org/10.5194/acp-15-8381-2015, https://doi.org/10.5194/acp-15-8381-2015, 2015
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IASI spaceborne imagery is used to reconstruct temporal variations of flux and altitude of volcanic emissions via an inversion procedure. Ground-based UV measurements underestimate the SO2 flux by 1 order of magnitude due to ash-induced plume opacity. Assimilation of SO2 altitude, retrieved directly from IASI, should render the inversion scheme independent of the wind shear prerequisite. CALIOP LiDAR observations support the coexistence of SO2 and sulfate aerosols in the volcanic cloud.
G. Zeng, J. E. Williams, J. A. Fisher, L. K. Emmons, N. B. Jones, O. Morgenstern, J. Robinson, D. Smale, C. Paton-Walsh, and D. W. T. Griffith
Atmos. Chem. Phys., 15, 7217–7245, https://doi.org/10.5194/acp-15-7217-2015, https://doi.org/10.5194/acp-15-7217-2015, 2015
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We assess the impact of biogenic emissions on CO and HCHO in the Southern Hemisphere (SH), with simulations using different emission inventories. Differences in biogenic emissions result in large differences on modelled CO in the source and the remote regions. Substantial inter-model differences exist. Models significantly underestimate observed HCHO columns in the SH, suggesting missing sources in the models. Differences in the CO/OH/CH4 chemistry lead to differences in HCHO in remote regions.
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.
S. R. Arnold, L. K. Emmons, S. A. Monks, K. S. Law, D. A. Ridley, S. Turquety, S. Tilmes, J. L. Thomas, I. Bouarar, J. Flemming, V. Huijnen, J. Mao, B. N. Duncan, S. Steenrod, Y. Yoshida, J. Langner, and Y. Long
Atmos. Chem. Phys., 15, 6047–6068, https://doi.org/10.5194/acp-15-6047-2015, https://doi.org/10.5194/acp-15-6047-2015, 2015
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The extent to which forest fires produce the air pollutant and greenhouse gas ozone (O3) in the atmosphere at high latitudes in not well understood. We have compared how fire emissions produce O3 and its precursors in several models of atmospheric chemistry. We find enhancements in O3 in air dominated by fires in all models, which increase on average as fire emissions age. We also find that in situ O3 production in the Arctic is sensitive to details of organic chemistry and vertical lifting.
S. Tilmes, J.-F. Lamarque, L. K. Emmons, D. E. Kinnison, P.-L. Ma, X. Liu, S. Ghan, C. Bardeen, S. Arnold, M. Deeter, F. Vitt, T. Ryerson, J. W. Elkins, F. Moore, J. R. Spackman, and M. Val Martin
Geosci. Model Dev., 8, 1395–1426, https://doi.org/10.5194/gmd-8-1395-2015, https://doi.org/10.5194/gmd-8-1395-2015, 2015
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The Community Atmosphere Model (CAM), version 5, is now coupled to extensive tropospheric and stratospheric chemistry, called CAM5-chem, and is available in addition to CAM4-chem in the Community Earth System Model (CESM) version 1.2. Both configurations are well suited as tools for atmospheric chemistry modeling studies in the troposphere and lower stratosphere.
S. A. Monks, S. R. Arnold, L. K. Emmons, K. S. Law, S. Turquety, B. N. Duncan, J. Flemming, V. Huijnen, S. Tilmes, J. Langner, J. Mao, Y. Long, J. L. Thomas, S. D. Steenrod, J. C. Raut, C. Wilson, M. P. Chipperfield, G. S. Diskin, A. Weinheimer, H. Schlager, and G. Ancellet
Atmos. Chem. Phys., 15, 3575–3603, https://doi.org/10.5194/acp-15-3575-2015, https://doi.org/10.5194/acp-15-3575-2015, 2015
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Multi-model simulations of Arctic CO, O3 and OH are evaluated using observations. Models show highly variable concentrations but the relative importance of emission regions and types is robust across the models, demonstrating the importance of biomass burning as a source. Idealised tracer experiments suggest that some of the model spread is due to variations in simulated transport from Europe in winter and from Asia throughout the year.
M. Van Damme, L. Clarisse, E. Dammers, X. Liu, J. B. Nowak, C. Clerbaux, C. R. Flechard, C. Galy-Lacaux, W. Xu, J. A. Neuman, Y. S. Tang, M. A. Sutton, J. W. Erisman, and P. F. Coheur
Atmos. Meas. Tech., 8, 1575–1591, https://doi.org/10.5194/amt-8-1575-2015, https://doi.org/10.5194/amt-8-1575-2015, 2015
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In this study, comprehensive ground-based data sets (Europe, China, Africa and United States) are used to evaluate NH3 measurements from IASI. Global yearly and regional monthly comparisons show fair agreement, while hourly measurements are used to investigate the limitations of direct comparisons. In addition, dense airborne measurements are explored and show the highest correlation coefficients in this study. Finally, the urgent need for independent NH3 column measurements is discussed.
J. A. Fisher, S. R. Wilson, G. Zeng, J. E. Williams, L. K. Emmons, R. L. Langenfelds, P. B. Krummel, and L. P. Steele
Atmos. Chem. Phys., 15, 3217–3239, https://doi.org/10.5194/acp-15-3217-2015, https://doi.org/10.5194/acp-15-3217-2015, 2015
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The Southern Hemisphere (SH) serves as an important test bed for evaluating our understanding of the processes that drive the composition of the clean background atmosphere. Using data from two aircraft campaigns, combined with four atmospheric chemistry models, we find a large sensitivity in the remote SH to biogenic emissions and their subsequent chemistry and transport. Future model evaluation and measurement campaigns should prioritize reducing uncertainties in these processes.
J.-L. Lacour, L. Clarisse, J. Worden, M. Schneider, S. Barthlott, F. Hase, C. Risi, C. Clerbaux, D. Hurtmans, and P.-F. Coheur
Atmos. Meas. Tech., 8, 1447–1466, https://doi.org/10.5194/amt-8-1447-2015, https://doi.org/10.5194/amt-8-1447-2015, 2015
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This paper describes a cross-validation study of tropospheric δD (HDO/H2O ratio) profiles retrieved from IASI spectra (retrieval performed at ULB). We document how these profiles compare to profiles derived from TES/AURA sounder and from three ground-based FTIRs of the NDACC network (produced within the MUSICA project). We show that empirical differences are in agreement with the theoretical expected differences which are dominated by IASI observational and the smoothing error components.
M. Val Martin, C. L. Heald, J.-F. Lamarque, S. Tilmes, L. K. Emmons, and B. A. Schichtel
Atmos. Chem. Phys., 15, 2805–2823, https://doi.org/10.5194/acp-15-2805-2015, https://doi.org/10.5194/acp-15-2805-2015, 2015
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We present for the first time the relative effect of climate, emissions, and land use change on ozone and PM25 over the United States, focusing on the national parks. Air quality in 2050 will likely be dominated by emission patterns, but climate and land use changes alone can lead to a substantial increase in air pollution over most of the US, with important implications for O3 air quality, visibility and ecosystem health degradation in the national parks.
C. Viatte, K. Strong, J. Hannigan, E. Nussbaumer, L. K. Emmons, S. Conway, C. Paton-Walsh, J. Hartley, J. Benmergui, and J. Lin
Atmos. Chem. Phys., 15, 2227–2246, https://doi.org/10.5194/acp-15-2227-2015, https://doi.org/10.5194/acp-15-2227-2015, 2015
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Seven tropospheric species (CO, HCN, C2H6, C2H2, CH3OH, HCOOH, and H2CO) released by biomass burning events transported to the high Arctic were monitored with two sets of FTIR measurements, located at Eureka (Nunavut, Canada) and Thule (Greenland), from 2008 to 2012. We compared these data sets with the MOZART-4 chemical transport model to help improve its simulations in the Arctic. Emission factors of these biomass burning products were derived and compared to the literature.
L. Hoffmann, M. J. Alexander, C. Clerbaux, A. W. Grimsdell, C. I. Meyer, T. Rößler, and B. Tournier
Atmos. Meas. Tech., 7, 4517–4537, https://doi.org/10.5194/amt-7-4517-2014, https://doi.org/10.5194/amt-7-4517-2014, 2014
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We present stratospheric gravity wave observations from 4.3 micron radiance measurements by the nadir sounders AIRS and IASI. Three case studies demonstrate that AIRS and IASI provide a consistent picture of the temporal development of individual gravity wave events. Statistical comparisons based on five years of data (2008-2012) also showed similar patterns of gravity wave activity. Long-term records from combined satellite data are an exciting prospect for future gravity wave research.
C. Crevoisier, C. Clerbaux, V. Guidard, T. Phulpin, R. Armante, B. Barret, C. Camy-Peyret, J.-P. Chaboureau, P.-F. Coheur, L. Crépeau, G. Dufour, L. Labonnote, L. Lavanant, J. Hadji-Lazaro, H. Herbin, N. Jacquinet-Husson, S. Payan, E. Péquignot, C. Pierangelo, P. Sellitto, and C. Stubenrauch
Atmos. Meas. Tech., 7, 4367–4385, https://doi.org/10.5194/amt-7-4367-2014, https://doi.org/10.5194/amt-7-4367-2014, 2014
T. Amnuaylojaroen, M. C. Barth, L. K. Emmons, G. R. Carmichael, J. Kreasuwun, S. Prasitwattanaseree, and S. Chantara
Atmos. Chem. Phys., 14, 12983–13012, https://doi.org/10.5194/acp-14-12983-2014, https://doi.org/10.5194/acp-14-12983-2014, 2014
H. Oetjen, V. H. Payne, S. S. Kulawik, A. Eldering, J. Worden, D. P. Edwards, G. L. Francis, H. M. Worden, C. Clerbaux, J. Hadji-Lazaro, and D. Hurtmans
Atmos. Meas. Tech., 7, 4223–4236, https://doi.org/10.5194/amt-7-4223-2014, https://doi.org/10.5194/amt-7-4223-2014, 2014
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We apply the TES ozone retrieval algorithm to IASI radiances and characterise the uncertainties and information content of the retrieved ozone profiles. We find that our biases with respect to sondes and our degrees of freedom for signal for ozone are comparable to previously published results from other IASI ozone algorithms. We find that predicted and empirical errors are consistent. In general, the precision of the IASI ozone profiles is better than 20%.
F. L. Herron-Thorpe, G. H. Mount, L. K. Emmons, B. K. Lamb, D. A. Jaffe, N. L. Wigder, S. H. Chung, R. Zhang, M. D. Woelfle, and J. K. Vaughan
Atmos. Chem. Phys., 14, 12533–12551, https://doi.org/10.5194/acp-14-12533-2014, https://doi.org/10.5194/acp-14-12533-2014, 2014
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Wildfire season simulations from an air quality forecast system for the Pacific Northwest were compared to surface monitor observations across the region and NASA Earth Observing System satellite retrievals of plume top, nitrogen dioxide, aerosol optical depth, and carbon monoxide. This study discusses why the Community Multi-scale Air Quality model predictions under-predicted secondary organic aerosol (SOA) production for events when fire emissions were transported large distances.
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
M. N. Deeter, S. Martínez-Alonso, D. P. Edwards, L. K. Emmons, J. C. Gille, H. M. Worden, C. Sweeney, J. V. Pittman, B. C. Daube, and S. C. Wofsy
Atmos. Meas. Tech., 7, 3623–3632, https://doi.org/10.5194/amt-7-3623-2014, https://doi.org/10.5194/amt-7-3623-2014, 2014
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The MOPITT Version 6 product for carbon monoxide (CO) incorporates several enhancements. First, a geolocation bias has been eliminated. Second, the new variable a priori for CO concentrations is based on simulations performed with the CAM-Chem chemical transport model for the years 2000-2009. Third, required meteorological fields are extracted from the MERRA reanalysis. Finally, a retrieval bias in the upper troposphere was substantially reduced. Validation results are presented.
I. B. Konovalov, E. V. Berezin, P. Ciais, G. Broquet, M. Beekmann, J. Hadji-Lazaro, C. Clerbaux, M. O. Andreae, J. W. Kaiser, and E.-D. Schulze
Atmos. Chem. Phys., 14, 10383–10410, https://doi.org/10.5194/acp-14-10383-2014, https://doi.org/10.5194/acp-14-10383-2014, 2014
S. Safieddine, A. Boynard, P.-F. Coheur, D. Hurtmans, G. Pfister, B. Quennehen, J. L. Thomas, J.-C. Raut, K. S. Law, Z. Klimont, J. Hadji-Lazaro, M. George, and C. Clerbaux
Atmos. Chem. Phys., 14, 10119–10131, https://doi.org/10.5194/acp-14-10119-2014, https://doi.org/10.5194/acp-14-10119-2014, 2014
J. D. Fast, J. Allan, R. Bahreini, J. Craven, L. Emmons, R. Ferrare, P. L. Hayes, A. Hodzic, J. Holloway, C. Hostetler, J. L. Jimenez, H. Jonsson, S. Liu, Y. Liu, A. Metcalf, A. Middlebrook, J. Nowak, M. Pekour, A. Perring, L. Russell, A. Sedlacek, J. Seinfeld, A. Setyan, J. Shilling, M. Shrivastava, S. Springston, C. Song, R. Subramanian, J. W. Taylor, V. Vinoj, Q. Yang, R. A. Zaveri, and Q. Zhang
Atmos. Chem. Phys., 14, 10013–10060, https://doi.org/10.5194/acp-14-10013-2014, https://doi.org/10.5194/acp-14-10013-2014, 2014
O. Stein, M. G. Schultz, I. Bouarar, H. Clark, V. Huijnen, A. Gaudel, M. George, and C. Clerbaux
Atmos. Chem. Phys., 14, 9295–9316, https://doi.org/10.5194/acp-14-9295-2014, https://doi.org/10.5194/acp-14-9295-2014, 2014
M. Li, Q. Zhang, D. G. Streets, K. B. He, Y. F. Cheng, L. K. Emmons, H. Huo, S. C. Kang, Z. Lu, M. Shao, H. Su, X. Yu, and Y. Zhang
Atmos. Chem. Phys., 14, 5617–5638, https://doi.org/10.5194/acp-14-5617-2014, https://doi.org/10.5194/acp-14-5617-2014, 2014
M. Pommier, J.-L. Lacour, C. Risi, F. M. Bréon, C. Clerbaux, P.-F. Coheur, K. Gribanov, D. Hurtmans, J. Jouzel, and V. Zakharov
Atmos. Meas. Tech., 7, 1581–1595, https://doi.org/10.5194/amt-7-1581-2014, https://doi.org/10.5194/amt-7-1581-2014, 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
H. Brenot, N. Theys, L. Clarisse, J. van Geffen, J. van Gent, M. Van Roozendael, R. van der A, D. Hurtmans, P.-F. Coheur, C. Clerbaux, P. Valks, P. Hedelt, F. Prata, O. Rasson, K. Sievers, and C. Zehner
Nat. Hazards Earth Syst. Sci., 14, 1099–1123, https://doi.org/10.5194/nhess-14-1099-2014, https://doi.org/10.5194/nhess-14-1099-2014, 2014
L. Clarisse, P.-F. Coheur, N. Theys, D. Hurtmans, and C. Clerbaux
Atmos. Chem. Phys., 14, 3095–3111, https://doi.org/10.5194/acp-14-3095-2014, https://doi.org/10.5194/acp-14-3095-2014, 2014
M. Van Damme, L. Clarisse, C. L. Heald, D. Hurtmans, Y. Ngadi, C. Clerbaux, A. J. Dolman, J. W. Erisman, and P. F. Coheur
Atmos. Chem. Phys., 14, 2905–2922, https://doi.org/10.5194/acp-14-2905-2014, https://doi.org/10.5194/acp-14-2905-2014, 2014
D. Griffin, K. A. Walker, J. E. Franklin, M. Parrington, C. Whaley, J. Hopper, J. R. Drummond, P. I. Palmer, K. Strong, T. J. Duck, I. Abboud, P. F. Bernath, C. Clerbaux, P.-F. Coheur, K. R. Curry, L. Dan, E. Hyer, J. Kliever, G. Lesins, M. Maurice, A. Saha, K. Tereszchuk, and D. Weaver
Atmos. Chem. Phys., 13, 10227–10241, https://doi.org/10.5194/acp-13-10227-2013, https://doi.org/10.5194/acp-13-10227-2013, 2013
M. Boichu, L. Menut, D. Khvorostyanov, L. Clarisse, C. Clerbaux, S. Turquety, and P.-F. Coheur
Atmos. Chem. Phys., 13, 8569–8584, https://doi.org/10.5194/acp-13-8569-2013, https://doi.org/10.5194/acp-13-8569-2013, 2013
F. Jégou, G. Berthet, C. Brogniez, J.-B. Renard, P. François, J. M. Haywood, A. Jones, Q. Bourgeois, T. Lurton, F. Auriol, S. Godin-Beekmann, C. Guimbaud, G. Krysztofiak, B. Gaubicher, M. Chartier, L. Clarisse, C. Clerbaux, J. Y. Balois, C. Verwaerde, and D. Daugeron
Atmos. Chem. Phys., 13, 6533–6552, https://doi.org/10.5194/acp-13-6533-2013, https://doi.org/10.5194/acp-13-6533-2013, 2013
N. Theys, R. Campion, L. Clarisse, H. Brenot, J. van Gent, B. Dils, S. Corradini, L. Merucci, P.-F. Coheur, M. Van Roozendael, D. Hurtmans, C. Clerbaux, S. Tait, and F. Ferrucci
Atmos. Chem. Phys., 13, 5945–5968, https://doi.org/10.5194/acp-13-5945-2013, https://doi.org/10.5194/acp-13-5945-2013, 2013
M. Krol, W. Peters, P. Hooghiemstra, M. George, C. Clerbaux, D. Hurtmans, D. McInerney, F. Sedano, P. Bergamaschi, M. El Hajj, J. W. Kaiser, D. Fisher, V. Yershov, and J.-P. Muller
Atmos. Chem. Phys., 13, 4737–4747, https://doi.org/10.5194/acp-13-4737-2013, https://doi.org/10.5194/acp-13-4737-2013, 2013
K. A. Tereszchuk, G. González Abad, C. Clerbaux, J. Hadji-Lazaro, D. Hurtmans, P.-F. Coheur, and P. F. Bernath
Atmos. Chem. Phys., 13, 4529–4541, https://doi.org/10.5194/acp-13-4529-2013, https://doi.org/10.5194/acp-13-4529-2013, 2013
A. Inness, F. Baier, A. Benedetti, I. Bouarar, S. Chabrillat, H. Clark, C. Clerbaux, P. Coheur, R. J. Engelen, Q. Errera, J. Flemming, M. George, C. Granier, J. Hadji-Lazaro, V. Huijnen, D. Hurtmans, L. Jones, J. W. Kaiser, J. Kapsomenakis, K. Lefever, J. Leitão, M. Razinger, A. Richter, M. G. Schultz, A. J. Simmons, M. Suttie, O. Stein, J.-N. Thépaut, V. Thouret, M. Vrekoussis, C. Zerefos, and the MACC team
Atmos. Chem. Phys., 13, 4073–4109, https://doi.org/10.5194/acp-13-4073-2013, https://doi.org/10.5194/acp-13-4073-2013, 2013
Y. R'Honi, L. Clarisse, C. Clerbaux, D. Hurtmans, V. Duflot, S. Turquety, Y. Ngadi, and P.-F. Coheur
Atmos. Chem. Phys., 13, 4171–4181, https://doi.org/10.5194/acp-13-4171-2013, https://doi.org/10.5194/acp-13-4171-2013, 2013
J. L. Thomas, J.-C. Raut, K. S. Law, L. Marelle, G. Ancellet, F. Ravetta, J. D. Fast, G. Pfister, L. K. Emmons, G. S. Diskin, A. Weinheimer, A. Roiger, and H. Schlager
Atmos. Chem. Phys., 13, 3825–3848, https://doi.org/10.5194/acp-13-3825-2013, https://doi.org/10.5194/acp-13-3825-2013, 2013
V. Duflot, D. Hurtmans, L. Clarisse, Y. R'honi, C. Vigouroux, M. De Mazière, E. Mahieu, C. Servais, C. Clerbaux, and P.-F. Coheur
Atmos. Meas. Tech., 6, 917–925, https://doi.org/10.5194/amt-6-917-2013, https://doi.org/10.5194/amt-6-917-2013, 2013
J. Gazeaux, C. Clerbaux, M. George, J. Hadji-Lazaro, J. Kuttippurath, P.-F. Coheur, D. Hurtmans, T. Deshler, M. Kovilakam, P. Campbell, V. Guidard, F. Rabier, and J.-N. Thépaut
Atmos. Meas. Tech., 6, 613–620, https://doi.org/10.5194/amt-6-613-2013, https://doi.org/10.5194/amt-6-613-2013, 2013
L. Clarisse, P.-F. Coheur, F. Prata, J. Hadji-Lazaro, D. Hurtmans, and C. Clerbaux
Atmos. Chem. Phys., 13, 2195–2221, https://doi.org/10.5194/acp-13-2195-2013, https://doi.org/10.5194/acp-13-2195-2013, 2013
H. M. Worden, M. N. Deeter, C. Frankenberg, M. George, F. Nichitiu, J. Worden, I. Aben, K. W. Bowman, C. Clerbaux, P. F. Coheur, A. T. J. de Laat, R. Detweiler, J. R. Drummond, D. P. Edwards, J. C. Gille, D. Hurtmans, M. Luo, S. Martínez-Alonso, S. Massie, G. Pfister, and J. X. Warner
Atmos. Chem. Phys., 13, 837–850, https://doi.org/10.5194/acp-13-837-2013, https://doi.org/10.5194/acp-13-837-2013, 2013
L. K. Emmons, P. G. Hess, J.-F. Lamarque, and G. G. Pfister
Geosci. Model Dev., 5, 1531–1542, https://doi.org/10.5194/gmd-5-1531-2012, https://doi.org/10.5194/gmd-5-1531-2012, 2012
Related subject area
Subject: Gases | Research Activity: Remote Sensing | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Increase in carbon monoxide (CO) and aerosol optical depth (AOD) observed by satellites in the Northern Hemisphere over the summers of 2008–2023, linked to an increase in wildfires
Monitoring of total and off-road NOx emissions from Canadian oil sands surface mining using the Ozone Monitoring Instrument
Large reductions in satellite-derived and modelled European lower-tropospheric ozone during and after the COVID-19 pandemic (2020–2022)
Air quality trends and regimes in South Korea inferred from 2015–2023 surface and satellite observations
What can we learn about tropospheric OH from satellite observations of methane?
Identifying missing sources and reducing NOx emissions uncertainty over China using daily satellite data and a mass-conserving method
Feasibility of robust estimates of ozone production rates using a synergy of satellite observations, ground-based remote sensing, and models
Satellite Detection of NO2 Distributions and Comparison with Ground-Based Concentrations
Global Patterns and Trends in Ground-Level Ozone Chemical Formation Regimes from 1996 to 2022
Upper-tropospheric pollutants observed by MIPAS: geographic and seasonal variations
Comparing space-based to reported carbon monoxide emission estimates for Europe's iron and steel plants
Unleashing the potential of geostationary satellite observations in air quality forecasting through artificial intelligence techniques
Tropical upper-tropospheric trends in ozone and carbon monoxide (2005–2020): observational and model results
Global seasonal urban, industrial, and background NO2 estimated from TROPOMI satellite observations
Biosphere-atmosphere related processes influence trace-gas and aerosol satellite-model biases
Ground-based Tropospheric Ozone Measurements: Regional tropospheric ozone column trends from the TOAR-II/ HEGIFTOM homogenized datasets
Opposing trends in the peak and low ozone concentrations in eastern China: anthropogenic and meteorological influences
Quantifying biases in TROPESS AIRS, CrIS, and joint AIRS+OMI tropospheric ozone products using ozonesondes
Vertical profiles of global tropospheric nitrogen dioxide (NO2) obtained by cloud slicing the TROPOspheric Monitoring Instrument (TROPOMI)
Opinion: Beyond global means – novel space-based approaches to indirectly constrain the concentrations of and trends and variations in the tropospheric hydroxyl radical (OH)
Estimation of diurnal emissions of CO2 from thermal power plants using spaceborne IPDA lidar
Satellite-observed relationships between land cover, burned area, and atmospheric composition over the southern Amazon
Ammonia emission estimates using CrIS satellite observations over Europe
Insights into the long-term (2005–2021) spatiotemporal evolution of summer ozone production sensitivity in the Northern Hemisphere derived with the Ozone Monitoring Instrument (OMI)
Tropical tropospheric ozone distribution and trends from in situ and satellite data
Estimation of ground-level NO2 and its spatiotemporal variations in China using GEMS measurements and a nested machine learning model
Measurement Report: Diurnal Variability of NO2 and HCHO Lower Tropospheric Vertical Profiles in Southeastern Los Angeles
Investigation of the impact of satellite vertical sensitivity on long-term retrieved lower-tropospheric ozone trends
Quantifying the diurnal variation in atmospheric NO2 from Geostationary Environment Monitoring Spectrometer (GEMS) observations
State-wide California 2020 Carbon Dioxide Budget Estimated with OCO-2 and OCO-3 satellite data
Ammonia in the upper troposphere–lower stratosphere (UTLS): GLORIA airborne measurements for CAMS model evaluation in the Asian monsoon and in biomass burning plumes above the South Atlantic
A lightweight NO2-to-NOx conversion model for quantifying NOx emissions of point sources from NO2 satellite observations
Towards a sector-specific CO∕CO2 emission ratio: satellite-based observations of CO release from steel production in Germany
Monitoring European anthropogenic NOx emissions from space
Pyrogenic HONO seen from space: insights from global IASI observations
First evaluation of the GEMS formaldehyde product against TROPOMI and ground-based column measurements during the in-orbit test period
High-resolution mapping of nitrogen oxide emissions in large US cities from TROPOMI retrievals of tropospheric nitrogen dioxide columns
Quantifying the tropospheric ozone radiative effect and its temporal evolution in the satellite era
A satellite chronology of plumes from the April 2021 eruption of La Soufrière, St Vincent
Investigation of spatial and temporal variability in lower tropospheric ozone from RAL Space UV–Vis satellite products
Two years of satellite-based carbon dioxide emission quantification at the world's largest coal-fired power plants
Tropical tropospheric ozone and carbon monoxide distributions: characteristics, origins, and control factors, as seen by IAGOS and IASI
Investigation of the summer 2018 European ozone air pollution episodes using novel satellite data and modelling
Bridging the spatial gaps of the Ammonia Monitoring Network using satellite ammonia measurements
A roadmap to estimating agricultural ammonia volatilization over Europe using satellite observations and simulation data
Investigation of meteorological conditions and BrO during ozone depletion events in Ny-Ålesund between 2010 and 2021
Quantification of carbon monoxide emissions from African cities using TROPOMI
Nitrogen oxides emissions from selected cities in North America, Europe, and East Asia observed by the TROPOspheric Monitoring Instrument (TROPOMI) before and after the COVID-19 pandemic
Remotely sensed and surface measurement- derived mass-conserving inversion of daily NOx emissions and inferred combustion technologies in energy-rich northern China
Examining TROPOMI formaldehyde to nitrogen dioxide ratios in the Lake Michigan region: implications for ozone exceedances
Antoine Ehret, Solène Turquety, Maya George, Juliette Hadji-Lazaro, and Cathy Clerbaux
Atmos. Chem. Phys., 25, 6365–6394, https://doi.org/10.5194/acp-25-6365-2025, https://doi.org/10.5194/acp-25-6365-2025, 2025
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Biomass burning has a considerable effect on the chemical composition of the atmosphere and climate, due to the emission of trace gases and aerosols. We examine the relationship between fire variability and the values of carbon monoxide and aerosol optical depth observed by satellites. The observed increase in wildfires has led to a corresponding rise in the mean and extreme values of carbon monoxide and aerosol optical depth during the summer and early autumn across the Northern Hemisphere.
Chris A. McLinden, Debora Griffin, Vitali Fioletov, Junhua Zhang, Enrico Dammers, Cristen Adams, Mallory Loria, Nickolay Krotkov, and Lok N. Lamsal
Atmos. Chem. Phys., 25, 6093–6120, https://doi.org/10.5194/acp-25-6093-2025, https://doi.org/10.5194/acp-25-6093-2025, 2025
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The Ozone Monitoring Instrument (OMI) was used to understand the evolution of NOx emissions from the Canadian oil sands. OMI NO2 combined with winds and reported stack emissions found emissions from the heavy-hauler mine fleet have remained flat since 2005, whereas the total oil sands mined have more than doubled. This difference is a result of emissions standards that limit NOx emissions becoming more stringent over this period, confirming the efficacy of the policy enacting these standards.
Matilda A. Pimlott, Richard J. Pope, Brian J. Kerridge, Richard Siddans, Barry G. Latter, Lucy J. Ventress, Wuhu Feng, and Martyn P. Chipperfield
Atmos. Chem. Phys., 25, 4391–4401, https://doi.org/10.5194/acp-25-4391-2025, https://doi.org/10.5194/acp-25-4391-2025, 2025
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Globally, lockdowns were implemented to limit the spread of COVID-19, leading to a decrease in emissions of key air pollutants. Here, we use novel satellite data and a chemistry model to investigate the impact of the pandemic on tropospheric ozone (O3), a key pollutant, in 2020. Overall, we found substantial decreases of up to 20 %, two-thirds of which came from emission reductions, while one-third was due to a decrease in the stratospheric O3 flux into the troposphere.
Yujin J. Oak, Daniel J. Jacob, Drew C. Pendergrass, Ruijun Dang, Nadia K. Colombi, Heesung Chong, Seoyoung Lee, Su Keun Kuk, and Jhoon Kim
Atmos. Chem. Phys., 25, 3233–3252, https://doi.org/10.5194/acp-25-3233-2025, https://doi.org/10.5194/acp-25-3233-2025, 2025
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We analyze 2015–2023 air quality trends in South Korea using surface and satellite observations. Primary pollutants have decreased, consistent with emissions reductions. Surface O3 continues to increase and PM2.5 has decreased overall, but the nitrate component has not. O3 and PM2.5 nitrate depend on nonlinear responses from precursor emissions. Satellite data indicate a recent shift to NOx-sensitive O3 and nitrate formation, where further NOx reductions will benefit both O3 and PM2.5 pollution.
Elise Penn, Daniel J. Jacob, Zichong Chen, James D. East, Melissa P. Sulprizio, Lori Bruhwiler, Joannes D. Maasakkers, Hannah Nesser, Zhen Qu, Yuzhong Zhang, and John Worden
Atmos. Chem. Phys., 25, 2947–2965, https://doi.org/10.5194/acp-25-2947-2025, https://doi.org/10.5194/acp-25-2947-2025, 2025
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The hydroxyl radical (OH) destroys many air pollutants, including methane. Global-mean OH cannot be directly measured, and thus it is inferred with the methyl chloroform (MCF) proxy. MCF is decreasing, and a replacement is needed. We use satellite observations of methane in two spectral ranges as a proxy for OH. We find shortwave infrared observations can characterize yearly OH and its seasonality but not the latitudinal distribution. Thermal infrared observations add little information.
Lingxiao Lu, Jason Blake Cohen, Kai Qin, Xiaolu Li, and Qin He
Atmos. Chem. Phys., 25, 2291–2309, https://doi.org/10.5194/acp-25-2291-2025, https://doi.org/10.5194/acp-25-2291-2025, 2025
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This study applies an approach that assimilates NO2 vertical column densities from TROPOMI in a mass-conserving manner and inverts daily NOx emissions, presented over rapidly changing regions in China. Source attribution is quantified by the local thermodynamics of the combustion temperature (NOx/NO2). Emission results identify sources which do not exist in the a priori datasets, especially medium industrial sources located next to the Yangtze River.
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.
Summer Joy Acker, Tracey Holloway, and Monica K. Harkey
EGUsphere, https://doi.org/10.5194/egusphere-2025-226, https://doi.org/10.5194/egusphere-2025-226, 2025
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Nitrogen dioxide (NO2) is a harmful air pollutant linked to heart and lung diseases, regulated in the U.S. through annual and 1-hour standards. Most areas lack ground monitors, so satellites can help fill this gap. While past studies showed satellites capture annual NO2 patterns well, we assess their ability to reflect 1-hour pollution levels. We find satellites perform best farther from roads and in winter. TEMPO, a new satellite taking hourly measurements, improves the detection of higher NO2.
Yu Tian, Siyi Wang, and Xiaomeng Jin
EGUsphere, https://doi.org/10.5194/egusphere-2025-368, https://doi.org/10.5194/egusphere-2025-368, 2025
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We leverage over two-decade ground-based ozone observations alongside space-based observations of ozone precursors (NO2 and formaldehyde) to study the long-term evolution in ozone chemical regimes across global source regions. We find a global trend towards NOx-limited regimes, supported by increasing satellite-based HCHO/NO2 and a diminishing ozone weekend effect.
Norbert Glatthor, Gabriele P. Stiller, Thomas von Clarmann, Bernd Funke, Sylvia Kellmann, and Andrea Linden
Atmos. Chem. Phys., 25, 1175–1208, https://doi.org/10.5194/acp-25-1175-2025, https://doi.org/10.5194/acp-25-1175-2025, 2025
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We present global upper-tropospheric distributions of the pollutants HCN, CO, C2H2, C2H6, PAN, and HCOOH, observed between 2002 and 2012 by the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) on the Environmental Satellite (Envisat). By comparing the spatial distributions of their volume mixing ratios and by global correlation and regression analyses, we draw conclusions on their sources, such as biomass burning, anthropogenic sources, and biogenic release.
Gijs Leguijt, Joannes D. Maasakkers, Hugo A. C. Denier van der Gon, Arjo J. Segers, Tobias Borsdorff, Ivar R. van der Velde, and Ilse Aben
Atmos. Chem. Phys., 25, 555–574, https://doi.org/10.5194/acp-25-555-2025, https://doi.org/10.5194/acp-25-555-2025, 2025
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The production of steel coincides with large emissions of greenhouse gases and air pollutants including carbon monoxide. European facilities are required to report their emissions, which are estimated using a variety of methods. We evaluate these estimates using carbon monoxide concentrations measured via satellite. We find generally good agreement between our values and those reported but also identify some uncertainties, showing that satellites can provide insights into these emissions.
Chengxin Zhang, Xinhan Niu, Hongyu Wu, Zhipeng Ding, Ka Lok Chan, Jhoon Kim, Thomas Wagner, and Cheng Liu
Atmos. Chem. Phys., 25, 759–770, https://doi.org/10.5194/acp-25-759-2025, https://doi.org/10.5194/acp-25-759-2025, 2025
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This research utilizes hourly air pollution observations from the world’s first geostationary satellite to develop a spatiotemporal neural network model for full-coverage surface NO2 pollution prediction over the next 24 hours, achieving outstanding forecasting performance and efficacy. These results highlight the profound impact of geostationary satellite observations in advancing air quality forecasting models, thereby contributing to future models for health exposure to air pollution.
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.
Vitali Fioletov, Chris A. McLinden, Debora Griffin, Xiaoyi Zhao, and Henk Eskes
Atmos. Chem. Phys., 25, 575–596, https://doi.org/10.5194/acp-25-575-2025, https://doi.org/10.5194/acp-25-575-2025, 2025
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Satellite data were used to estimate urban per capita emissions for 261 major cities worldwide. Three components in tropospheric NO2 data (background NO2, NO2 from urban sources, and NO2 from industrial point sources) were isolated, and then each of these components was analyzed separately. The largest per capita emissions were found in the Middle East and the smallest in India and southern Africa. Urban weekend emissions are 20 %–50 % less than workday emissions for all regions except China.
Emma Sands, Ruth M. Doherty, Fiona M. O'Connor, Richard J. Pope, James Weber, and Daniel P. Grosvenor
EGUsphere, https://doi.org/10.5194/egusphere-2024-4014, https://doi.org/10.5194/egusphere-2024-4014, 2025
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We use satellite observations to quantify isoprene, formaldehyde and aerosol optical depth biases in UKESM1.1 and their sensitivity to process representation. The more detailed chemistry mechanism is particularly impactful by decreasing the isoprene and formaldehyde biases and reducing aerosol formation. Other processes have strong regional impacts. The new processes affect the present-day aerosol direct radiative effect (+0.17 W m-2), with implications for land use change forcing studies.
Roeland Van Malderen, Zhou Zang, Kai-Lan Chang, Robin Björklund, Owen R. Cooper, Jane Liu, Eliane Maillard Barras, Corinne Vigouroux, Irina Petropavlovskikh, Thierry Leblanc, Valérie Thouret, Pawel Wolff, Peter Effertz, Audrey Gaudel, David W. Tarasick, Herman G. J. Smit, Anne M. Thompson, Ryan M. Stauffer, Debra E. Kollonige, Deniz Poyraz, Gérard Ancellet, Marie-Renée De Backer, Matthias M. Frey, James W. Hannigan, José L. Hernandez, Bryan J. Johnson, Nicholas Jones, Rigel Kivi, Emmanuel Mahieu, Isamu Morino, Glen McConville, Katrin Müller, Isao Murata, Justus Notholt, Ankie Piters, Maxime Prignon, Richard Querel, Vincenzo Rizi, Dan Smale, Wolfgang Steinbrecht, Kimberly Strong, and Ralf Sussmann
EGUsphere, https://doi.org/10.5194/egusphere-2024-3745, https://doi.org/10.5194/egusphere-2024-3745, 2025
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Tropospheric ozone is an important greenhouse gas and an air pollutant, whose distribution and time variability is mainly governed by anthropogenic emissions and dynamics. In this paper, we assess regional trends of tropospheric ozone column amounts, based on two different approaches of merging or synthesizing ground-based observations and their trends within specific regions. Our findings clearly demonstrate regional trend differences, but also consistently higher pre- than post-COVID trends.
Zhuang Wang, Chune Shi, Hao Zhang, Xianguang Ji, Yizhi Zhu, Congzi Xia, Xiaoyun Sun, Xinfeng Lin, Shaowei Yan, Suyao Wang, Yuan Zhou, Chengzhi Xing, Yujia Chen, and Cheng Liu
Atmos. Chem. Phys., 25, 347–366, https://doi.org/10.5194/acp-25-347-2025, https://doi.org/10.5194/acp-25-347-2025, 2025
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This study attempts to explain the surface ozone background and typical and peak trends in eastern China by combining a large number of ground-based and satellite observations. We found diametrically opposed trends in peak (decreasing) and low (increasing) ozone concentrations. Anthropogenic emissions primarily drive trends in low and peak ozone concentrations in eastern China, though meteorological effects also play a role.
Elyse A. Pennington, Gregory B. Osterman, Vivienne H. Payne, Kazuyuki Miyazaki, Kevin W. Bowman, and Jessica L. Neu
EGUsphere, https://doi.org/10.5194/egusphere-2024-3701, https://doi.org/10.5194/egusphere-2024-3701, 2024
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Tropospheric ozone is a harmful pollutant & powerful greenhouse gas. For satellite products to accurately quantify trends in tropospheric ozone, they must have low bias compared to a reliable source of data. This study compares 3 TROPESS satellite products – CrIS, AIRS, & AIRSOMI – to ozonesonde data. They have low global measurement bias & thus can be used to detect global tropospheric ozone trends, but the measurement bias should be considered in certain regions & time periods.
Rebekah P. Horner, Eloise A. Marais, Nana Wei, Robert G. Ryan, and Viral Shah
Atmos. Chem. Phys., 24, 13047–13064, https://doi.org/10.5194/acp-24-13047-2024, https://doi.org/10.5194/acp-24-13047-2024, 2024
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Nitrogen oxides (NOx ≡ NO + NO2) affect tropospheric ozone and the hydroxyl radical, influencing climate and atmospheric oxidation. To address the lack of routine observations of NOx, we cloud slice satellite observations of NO2 to derive a new dataset of global vertical profiles of NO2. We evaluate our data against in situ aircraft observations and use these data to critique the contemporary understanding of tropospheric NOx, as simulated by the GEOS-Chem model.
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.
Xuanye Zhang, Hailong Yang, Lingbing Bu, Zengchang Fan, Wei Xiao, Binglong Chen, Lu Zhang, Sihan Liu, Zhongting Wang, Jiqiao Liu, Weibiao Chen, and Xuhui Lee
EGUsphere, https://doi.org/10.5194/egusphere-2024-3152, https://doi.org/10.5194/egusphere-2024-3152, 2024
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This study utilized the IPDA lidar aboard the DQ-1 satellite to monitor emissions from localized strong point sources and, for the first time, observed the diurnal variation of CO2 emissions from a high-latitude power plant, Overall, power plant CO2 emissions were largely consistent with local electricity consumption patterns, with most plants emitting less at night than during the day, and with higher emissions in winter and summer compared to spring and autumn.
Emma Sands, Richard J. Pope, Ruth M. Doherty, Fiona M. O'Connor, Chris Wilson, and Hugh Pumphrey
Atmos. Chem. Phys., 24, 11081–11102, https://doi.org/10.5194/acp-24-11081-2024, https://doi.org/10.5194/acp-24-11081-2024, 2024
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Changes in vegetation alongside biomass burning impact regional atmospheric composition and air quality. Using satellite remote sensing, we find a clear linear relationship between forest cover and isoprene and a pronounced non-linear relationship between burned area and nitrogen dioxide in the southern Amazon, a region of substantial deforestation. These quantified relationships can be used for model evaluation and further exploration of biosphere-atmosphere interactions in Earth System Models.
Jieying Ding, Ronald van der A, Henk Eskes, Enrico Dammers, Mark Shephard, Roy Wichink Kruit, Marc Guevara, and Leonor Tarrason
Atmos. Chem. Phys., 24, 10583–10599, https://doi.org/10.5194/acp-24-10583-2024, https://doi.org/10.5194/acp-24-10583-2024, 2024
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Here we applied the existing Daily Emissions Constrained by Satellite Observations (DECSO) inversion algorithm to NH3 observations from the CrIS satellite instrument to estimate NH3 emissions. As NH3 in the atmosphere is influenced by NOx, we implemented DECSO to estimate NOx and NH3 emissions simultaneously. The emissions are derived over Europe for 2020 at a spatial resolution of 0.2° using daily observations from CrIS and TROPOMI. Results are compared to bottom-up emission inventories.
Matthew S. Johnson, Sajeev Philip, Scott Meech, Rajesh Kumar, Meytar Sorek-Hamer, Yoichi P. Shiga, and Jia Jung
Atmos. Chem. Phys., 24, 10363–10384, https://doi.org/10.5194/acp-24-10363-2024, https://doi.org/10.5194/acp-24-10363-2024, 2024
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Satellites, like the Ozone Monitoring Instrument (OMI), retrieve proxy species of ozone (O3) formation (formaldehyde and nitrogen dioxide) and the ratios (FNRs) which can define O3 production sensitivity regimes. Here we investigate trends of OMI FNRs from 2005 to 2021, and they have increased in major cities, suggesting a transition from radical- to NOx-limited regimes. OMI also observed the impact of reduced emissions during the 2020 COVID-19 lockdown that resulted in increased FNRs.
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.
Naveed Ahmad, Changqing Lin, Alexis K. H. Lau, Jhoon Kim, Tianshu Zhang, Fangqun Yu, Chengcai Li, Ying Li, Jimmy C. H. Fung, and Xiang Qian Lao
Atmos. Chem. Phys., 24, 9645–9665, https://doi.org/10.5194/acp-24-9645-2024, https://doi.org/10.5194/acp-24-9645-2024, 2024
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This study developed a nested machine learning model to convert the GEMS NO2 column measurements into ground-level concentrations across China. The model directly incorporates the NO2 mixing height (NMH) into the methodological framework. The study underscores the importance of considering NMH when estimating ground-level NO2 from satellite column measurements and highlights the significant advantages of new-generation geostationary satellites in air quality monitoring.
Peter Peterson, Lisa Hernandez, Leslie Tanaka, and Alejandro Dunnick
EGUsphere, https://doi.org/10.5194/egusphere-2024-1460, https://doi.org/10.5194/egusphere-2024-1460, 2024
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This work uses spectroscopy to examine the vertical distribution of nitrogen dioxide and formaldehyde in southeastern Los Angeles, USA, a region heavily impacted by ozone pollution. We examine how both the amount and vertical profile of the two species varies throughout the day, finding that differences between the two species impact the utilization of satellite-based measurements to diagnose ozone production chemistry and these impacts are variable depending on the time of day.
Richard J. Pope, Fiona M. O'Connor, Mohit Dalvi, Brian J. Kerridge, Richard Siddans, Barry G. Latter, Brice Barret, Eric Le Flochmoen, Anne Boynard, Martyn P. Chipperfield, Wuhu Feng, Matilda A. Pimlott, Sandip S. Dhomse, Christian Retscher, Catherine Wespes, and Richard Rigby
Atmos. Chem. Phys., 24, 9177–9195, https://doi.org/10.5194/acp-24-9177-2024, https://doi.org/10.5194/acp-24-9177-2024, 2024
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Ozone is a potent air pollutant in the lower troposphere, with adverse impacts on human health. Satellite records of tropospheric ozone currently show large-scale inconsistencies in long-term trends. Our detailed study of the potential factors (e.g. satellite errors, where the satellite can observe ozone) potentially driving these inconsistencies found that, in North America, Europe, and East Asia, the underlying trends are typically small with large uncertainties.
David P. Edwards, Sara Martínez-Alonso, Duseong S. Jo, Ivan Ortega, Louisa K. Emmons, John J. Orlando, Helen M. Worden, Jhoon Kim, Hanlim Lee, Junsung Park, and Hyunkee Hong
Atmos. Chem. Phys., 24, 8943–8961, https://doi.org/10.5194/acp-24-8943-2024, https://doi.org/10.5194/acp-24-8943-2024, 2024
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Until recently, satellite observations of atmospheric pollutants at any location could only be obtained once a day. New geostationary satellites stare at a region of the Earth to make hourly measurements, and the Geostationary Environment Monitoring Spectrometer is the first looking at Asia. These data and model simulations show how the change seen for one important pollutant that determines air quality depends on a combination of pollution emissions, atmospheric chemistry, and meteorology.
Matthew S. Johnson, Sofia D. Hamilton, Seongeun Jeong, Yuyan Cui, Dien Wu, Alex Turner, and Marc Fischer
EGUsphere, https://doi.org/10.5194/egusphere-2024-2152, https://doi.org/10.5194/egusphere-2024-2152, 2024
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Satellites, such as NASA’s Orbiting Carbon Observatory-2 and -3 (OCO-2/3), retrieve carbon dioxide (CO2) concentrations which provide vital information for estimating surface CO2 emissions. Here we investigate the ability of OCO-2/3 retrievals to constrain CO2 emissions for the state of California for the major emission sectors (i.e., fossil fuels, net ecosystem exchange, wildfire).
Sören Johansson, Michael Höpfner, Felix Friedl-Vallon, Norbert Glatthor, Thomas Gulde, Vincent Huijnen, Anne Kleinert, Erik Kretschmer, Guido Maucher, Tom Neubert, Hans Nordmeyer, Christof Piesch, Peter Preusse, Martin Riese, Björn-Martin Sinnhuber, Jörn Ungermann, Gerald Wetzel, and Wolfgang Woiwode
Atmos. Chem. Phys., 24, 8125–8138, https://doi.org/10.5194/acp-24-8125-2024, https://doi.org/10.5194/acp-24-8125-2024, 2024
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We present airborne infrared limb sounding GLORIA measurements of ammonia (NH3) in the upper troposphere of air masses within the Asian monsoon and of those connected with biomass burning. Comparing CAMS (Copernicus Atmosphere Monitoring Service) model data, we find that the model reproduces the measured enhanced NH3 within the Asian monsoon well but not that within biomass burning plumes, where no enhanced NH3 is measured in the upper troposphere but considerable amounts are simulated by CAMS.
Sandro Meier, Erik F. M. Koene, Maarten Krol, Dominik Brunner, Alexander Damm, and Gerrit Kuhlmann
Atmos. Chem. Phys., 24, 7667–7686, https://doi.org/10.5194/acp-24-7667-2024, https://doi.org/10.5194/acp-24-7667-2024, 2024
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Nitrogen oxides (NOx = NO + NO2) are important air pollutants. This study addresses the challenge of accurately estimating NOx emissions from NO2 satellite observations. We develop a realistic model to convert NO2 to NOx by using simulated plumes from various power plants. We apply the model to satellite NO2 observations, significantly reducing biases in estimated NOx emissions. The study highlights the potential for a consistent, high-resolution estimation of NOx emissions using satellite data.
Oliver Schneising, Michael Buchwitz, Maximilian Reuter, Michael Weimer, Heinrich Bovensmann, John P. Burrows, and Hartmut Bösch
Atmos. Chem. Phys., 24, 7609–7621, https://doi.org/10.5194/acp-24-7609-2024, https://doi.org/10.5194/acp-24-7609-2024, 2024
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Large quantities of CO and CO2 are emitted during conventional steel production. As satellite-based estimates of CO2 emissions at the facility level are challenging, co-emitted CO can indicate the carbon footprint of steel plants. We estimate CO emissions for German steelworks and use CO2 emissions from emissions trading data to derive a sector-specific CO/CO2 emission ratio for the steel industry; it is a prerequisite to use CO as a proxy for CO2 emissions from similar steel production sites.
Ronald J. van der A, Jieying Ding, and Henk Eskes
Atmos. Chem. Phys., 24, 7523–7534, https://doi.org/10.5194/acp-24-7523-2024, https://doi.org/10.5194/acp-24-7523-2024, 2024
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Using observations of the Sentinel-5P satellite and the latest version of the inversion algorithm DECSO, anthropogenic NOx emissions are derived for Europe for the years 2019–2022 with a spatial resolution of 0.2°. The results are compared with European emissions of the Copernicus Atmosphere Monitoring Service.
Bruno Franco, Lieven Clarisse, Nicolas Theys, Juliette Hadji-Lazaro, Cathy Clerbaux, and Pierre Coheur
Atmos. Chem. Phys., 24, 4973–5007, https://doi.org/10.5194/acp-24-4973-2024, https://doi.org/10.5194/acp-24-4973-2024, 2024
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Using IASI global infrared measurements, we retrieve nitrous acid (HONO) in fire plumes from space. We detect large enhancements of pyrogenic HONO worldwide, especially from intense wildfires at Northern Hemisphere mid- and high latitudes. Predominance of IASI nighttime over daytime measurements sheds light on HONO's extended lifetime and secondary formation during long-range transport in smoke plumes. Our findings deepen the understanding of atmospheric HONO, crucial for air quality assessment.
Gitaek T. Lee, Rokjin J. Park, Hyeong-Ahn Kwon, Eunjo S. Ha, Sieun D. Lee, Seunga Shin, Myoung-Hwan Ahn, Mina Kang, Yong-Sang Choi, Gyuyeon Kim, Dong-Won Lee, Deok-Rae Kim, Hyunkee Hong, Bavo Langerock, Corinne Vigouroux, Christophe Lerot, Francois Hendrick, Gaia Pinardi, Isabelle De Smedt, Michel Van Roozendael, Pucai Wang, Heesung Chong, Yeseul Cho, and Jhoon Kim
Atmos. Chem. Phys., 24, 4733–4749, https://doi.org/10.5194/acp-24-4733-2024, https://doi.org/10.5194/acp-24-4733-2024, 2024
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This study evaluates the Geostationary Environment Monitoring Spectrometer (GEMS) HCHO product by comparing its vertical column densities (VCDs) with those of TROPOMI and ground-based observations. Based on some sensitivity tests, obtaining radiance references under clear-sky conditions significantly improves HCHO retrieval quality. GEMS HCHO VCDs captured seasonal and diurnal variations well during the first year of observation, showing consistency with TROPOMI and ground-based observations.
Fei Liu, Steffen Beirle, Joanna Joiner, Sungyeon Choi, Zhining Tao, K. Emma Knowland, Steven J. Smith, Daniel Q. Tong, Siqi Ma, Zachary T. Fasnacht, and Thomas Wagner
Atmos. Chem. Phys., 24, 3717–3728, https://doi.org/10.5194/acp-24-3717-2024, https://doi.org/10.5194/acp-24-3717-2024, 2024
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Using satellite data, we developed a coupled method independent of the chemical transport model to map NOx emissions across US cities. After validating our technique with synthetic data, we charted NOx emissions from 2018–2021 in 39 cities. Our results closely matched EPA estimates but also highlighted some inconsistencies in both magnitude and spatial distribution. This research can help refine strategies for monitoring and managing air quality.
Richard J. Pope, Alexandru Rap, Matilda A. Pimlott, Brice Barret, Eric Le Flochmoen, Brian J. Kerridge, Richard Siddans, Barry G. Latter, Lucy J. Ventress, Anne Boynard, Christian Retscher, Wuhu Feng, Richard Rigby, Sandip S. Dhomse, Catherine Wespes, and Martyn P. Chipperfield
Atmos. Chem. Phys., 24, 3613–3626, https://doi.org/10.5194/acp-24-3613-2024, https://doi.org/10.5194/acp-24-3613-2024, 2024
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Tropospheric ozone is an important short-lived climate forcer which influences the incoming solar short-wave radiation and the outgoing long-wave radiation in the atmosphere (8–15 km) where the balance between the two yields a net positive (i.e. warming) effect at the surface. Overall, we find that the tropospheric ozone radiative effect ranges between 1.21 and 1.26 W m−2 with a negligible trend (2008–2017), suggesting that tropospheric ozone influences on climate have remained stable with time.
Isabelle A. Taylor, Roy G. Grainger, Andrew T. Prata, Simon R. Proud, Tamsin A. Mather, and David M. Pyle
Atmos. Chem. Phys., 23, 15209–15234, https://doi.org/10.5194/acp-23-15209-2023, https://doi.org/10.5194/acp-23-15209-2023, 2023
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This study looks at sulfur dioxide (SO2) and ash emissions from the April 2021 eruption of La Soufrière on St Vincent. Using satellite data, 35 eruptive events were identified. Satellite data were used to track SO2 as it was transported around the globe. The majority of SO2 was emitted into the upper troposphere and lower stratosphere. Similarities with the 1979 eruption of La Soufrière highlight the value of studying these eruptions to be better prepared for future eruptions.
Richard J. Pope, Brian J. Kerridge, Richard Siddans, Barry G. Latter, Martyn P. Chipperfield, Wuhu Feng, Matilda A. Pimlott, Sandip S. Dhomse, Christian Retscher, and Richard Rigby
Atmos. Chem. Phys., 23, 14933–14947, https://doi.org/10.5194/acp-23-14933-2023, https://doi.org/10.5194/acp-23-14933-2023, 2023
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Ozone is a potent air pollutant, and we present the first study to investigate long-term changes in lower tropospheric column ozone (LTCO3) from space. We have constructed a merged LTCO3 dataset from GOME-1, SCIAMACHY and OMI between 1996 and 2017. Comparing LTCO3 between the 1996–2000 and 2013–2017 5-year averages, we find significant positive increases in the tropics/sub-tropics, while in the northern mid-latitudes, we find small-scale differences.
Daniel H. Cusworth, Andrew K. Thorpe, Charles E. Miller, Alana K. Ayasse, Ralph Jiorle, Riley M. Duren, Ray Nassar, Jon-Paul Mastrogiacomo, and Robert R. Nelson
Atmos. Chem. Phys., 23, 14577–14591, https://doi.org/10.5194/acp-23-14577-2023, https://doi.org/10.5194/acp-23-14577-2023, 2023
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Carbon dioxide (CO2) emissions from combustion sources are uncertain in many places across the globe. Satellites have the ability to detect and quantify emissions from large CO2 point sources, including coal-fired power plants. In this study, we tasked two satellites to routinely observe CO2 emissions at 30 coal-fired power plants between 2021 and 2022. These results present the largest dataset of space-based CO2 emission estimates to date.
Maria Tsivlidou, Bastien Sauvage, Yasmine Bennouna, Romain Blot, Damien Boulanger, Hannah Clark, Eric Le Flochmoën, Philippe Nédélec, Valérie Thouret, Pawel Wolff, and Brice Barret
Atmos. Chem. Phys., 23, 14039–14063, https://doi.org/10.5194/acp-23-14039-2023, https://doi.org/10.5194/acp-23-14039-2023, 2023
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The tropics are a region where the ozone increase has been most apparent since 1980 and where observations are sparse. Using aircraft, satellite, and model data, we document the characteristics of tropospheric ozone and CO over the whole tropics for the last 2 decades. We explore the origin of the observed CO anomalies and investigate transport processes driving the tropical CO and O3 distribution. Our study highlights the importance of anthropogenic emissions, mostly over the northern tropics.
Richard J. Pope, Brian J. Kerridge, Martyn P. Chipperfield, Richard Siddans, Barry G. Latter, Lucy J. Ventress, Matilda A. Pimlott, Wuhu Feng, Edward Comyn-Platt, Garry D. Hayman, Stephen R. Arnold, and Ailish M. Graham
Atmos. Chem. Phys., 23, 13235–13253, https://doi.org/10.5194/acp-23-13235-2023, https://doi.org/10.5194/acp-23-13235-2023, 2023
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In the summer of 2018, Europe experienced several persistent large-scale ozone (O3) pollution episodes. Satellite tropospheric O3 and surface O3 data recorded substantial enhancements in 2018 relative to other years. Targeted model simulations showed that meteorological processes and emissions controlled the elevated surface O3, while mid-tropospheric O3 enhancements were dominated by stratospheric O3 intrusion and advection of North Atlantic O3-rich air masses into Europe.
Rui Wang, Da Pan, Xuehui Guo, Kang Sun, Lieven Clarisse, Martin Van Damme, Pierre-François Coheur, Cathy Clerbaux, Melissa Puchalski, and Mark A. Zondlo
Atmos. Chem. Phys., 23, 13217–13234, https://doi.org/10.5194/acp-23-13217-2023, https://doi.org/10.5194/acp-23-13217-2023, 2023
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Ammonia (NH3) is a key precursor for fine particulate matter (PM2.5) and a primary form of reactive nitrogen, yet it has sparse ground measurements. We perform the first comprehensive comparison between ground observations and satellite retrievals in the US, demonstrating that satellite NH3 data can help fill spatial gaps in the current ground monitoring networks. Trend analyses using both datasets highlight increasing NH3 trends across the US, including the NH3 hotspots and urban areas.
Rimal Abeed, Camille Viatte, William C. Porter, Nikolaos Evangeliou, Cathy Clerbaux, Lieven Clarisse, Martin Van Damme, Pierre-François Coheur, and Sarah Safieddine
Atmos. Chem. Phys., 23, 12505–12523, https://doi.org/10.5194/acp-23-12505-2023, https://doi.org/10.5194/acp-23-12505-2023, 2023
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Ammonia emissions from agricultural activities will inevitably increase with the rise in population. We use a variety of datasets (satellite, reanalysis, and model simulation) to calculate the first regional map of ammonia emission potential during the start of the growing season in Europe. We then apply our developed method using a climate model to show the effect of the temperature increase on future ammonia columns under two possible climate scenarios.
Bianca Zilker, Andreas Richter, Anne-Marlene Blechschmidt, Peter von der Gathen, Ilias Bougoudis, Sora Seo, Tim Bösch, and John Philip Burrows
Atmos. Chem. Phys., 23, 9787–9814, https://doi.org/10.5194/acp-23-9787-2023, https://doi.org/10.5194/acp-23-9787-2023, 2023
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During Arctic spring, near-surface ozone is depleted by bromine released from salty sea ice and/or snow-covered areas under certain meteorological conditions. To study this ozone depletion and the prevailing meteorological conditions, two ozone data sets from Ny-Ålesund, Svalbard, have been evaluated. We found that during ozone depletion events lower pressure over the Barents Sea and higher pressure in the Icelandic Low area led to a transport of cold polar air from the north to Ny-Ålesund.
Gijs Leguijt, Joannes D. Maasakkers, Hugo A. C. Denier van der Gon, Arjo J. Segers, Tobias Borsdorff, and Ilse Aben
Atmos. Chem. Phys., 23, 8899–8919, https://doi.org/10.5194/acp-23-8899-2023, https://doi.org/10.5194/acp-23-8899-2023, 2023
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We present a fast method to evaluate carbon monoxide emissions from cities in Africa. Carbon monoxide is important for climate change in an indirect way, as it is linked to ozone, methane, and carbon dioxide. Our measurements are made with a satellite that sees the entire globe every single day. This means that we can check from space whether the current knowledge of emission rates is up to date. We make the comparison and show that the emission rates in northern Africa are underestimated.
Chantelle R. Lonsdale and Kang Sun
Atmos. Chem. Phys., 23, 8727–8748, https://doi.org/10.5194/acp-23-8727-2023, https://doi.org/10.5194/acp-23-8727-2023, 2023
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The COVID-19 pandemic, which was caused by the SARS-CoV-2 virus, emerged in 2019, and its still evolving variants have resulted in unprecedented shifts in human activities and anthropogenic emissions into the Earth's atmosphere. We present monthly nitrogen oxide emissions over three major continents from May 2018 to January 2023 to capture variations before and after the COVID-19 pandemic. We focus on a diverse collection of 54 cities to quantify the post-COVID-19 perturbations.
Xiaolu Li, Jason Blake Cohen, Kai Qin, Hong Geng, Xiaohui Wu, Liling Wu, Chengli Yang, Rui Zhang, and Liqin Zhang
Atmos. Chem. Phys., 23, 8001–8019, https://doi.org/10.5194/acp-23-8001-2023, https://doi.org/10.5194/acp-23-8001-2023, 2023
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Remotely sensed NO2 and surface NOx are combined with a mathematical method to estimate daily NOx emissions. The results identify new sources and improve existing estimates. The estimation is driven by three flexible factors: thermodynamics of combustion, chemical loss, and atmospheric transport. The thermodynamic term separates power, iron, and cement from coking, boilers, and aluminum. This work finds three causes for the extremes: emissions, UV radiation, and transport.
Juanito Jerrold Mariano Acdan, Robert Bradley Pierce, Angela F. Dickens, Zachariah Adelman, and Tsengel Nergui
Atmos. Chem. Phys., 23, 7867–7885, https://doi.org/10.5194/acp-23-7867-2023, https://doi.org/10.5194/acp-23-7867-2023, 2023
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Ozone is an air pollutant that is harmful to human health. Near the surface of Earth, ozone is created when other pollutants react in the presence of sunlight. This study uses satellite data to investigate how ozone levels can be decreased in the Lake Michigan region of the United States. Our results indicate that ozone levels can be decreased by decreasing volatile organic compound emissions in urban areas and decreasing nitrogen oxide emissions in the region as a whole.
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Short summary
In this paper, we assess how daily ozone measurements from the Infrared Atmospheric Sounding Interferometer (IASI/MetOp) can contribute to the analyses of the processes driving O3 variability in the troposphere and the stratosphere with a set of parameterized geophysical variables, and we demonstrate the added value of IASI exceptional frequency sampling for monitoring medium- to long-term changes in global ozone concentrations in the future.
In this paper, we assess how daily ozone measurements from the Infrared Atmospheric Sounding...
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