Articles | Volume 18, issue 7
https://doi.org/10.5194/amt-18-1675-2025
© Author(s) 2025. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/amt-18-1675-2025
© Author(s) 2025. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Research article
| 
11 Apr 2025
Research article |
| 11 Apr 2025
| 11 Apr 2025
Deep transfer learning method for seasonal TROPOMI XCH4 albedo correction
Alexander C. Bradley
Cooperative Institute for Research in Environmental Sciences, University of Colorado, Boulder, CO 80309, USA
Chemistry Department, University of Colorado, Boulder, CO 80309, USA
Barbara Dix
Chemistry Department, University of Colorado, Boulder, CO 80309, USA
Fergus Mackenzie
BlueSky Resources, Boulder CO 80302, USA
J. Pepijn Veefkind
Royal Netherlands Meteorological Institute (KNMI), De Bilt, the Netherlands
Department of Geosciences and Remote Sensing, Delft University of Technology, Delft, the Netherlands
Joost A. de Gouw
CORRESPONDING AUTHOR
Cooperative Institute for Research in Environmental Sciences, University of Colorado, Boulder, CO 80309, USA
Chemistry Department, University of Colorado, Boulder, CO 80309, USA
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Martin de Graaf, Maarten Sneep, Mark ter Linden, L. Gijsbert Tilstra, David P. Donovan, Gerd-Jan van Zadelhoff, and J. Pepijn Veefkind
Atmos. Meas. Tech., 18, 2553–2571, https://doi.org/10.5194/amt-18-2553-2025, https://doi.org/10.5194/amt-18-2553-2025, 2025
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The aerosol layer height (ALH) from the TROPOspheric Monitoring Instrument (TROPOMI) has been constantly improved since its release in 2019. Over bright surfaces, fitting the albedo improved the retrieval, as shown for a set of situations, ranging from multiple layers of smoke to thick desert dust plumes and low-altitude industrial pollution. The latest results of the operational ALH are compared to profiles from the ATmospheric LIDar (ATLID) on board the recently launched EarthCARE mission.
Harikrishnan Charuvil Asokan, Jochen Landgraf, Pepijn Veefkind, Stijn Dellaert, and André Butz
EGUsphere, https://doi.org/10.5194/egusphere-2025-1071, https://doi.org/10.5194/egusphere-2025-1071, 2025
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Greenhouse gases like CO2 and CH4 drive climate change. Satellites enable monitoring of these emissions from space. Our simulations show that the upcoming TANGO mission can detect about 500 targets per 4-day cycle under clear skies, but cloud cover reduces detection. Integrating cloud forecasts into TANGO’s maneuvering boosts detections, highlighting its potential for improving global emission monitoring.
Michael F. Link, Megan S. Claflin, Christina E. Cecelski, Ayomide A. Akande, Delaney Kilgour, Paul A. Heine, Matthew Coggon, Chelsea E. Stockwell, Andrew Jensen, Jie Yu, Han N. Huynh, Jenna C. Ditto, Carsten Warneke, William Dresser, Keighan Gemmell, Spiro Jorga, Rileigh L. Robertson, Joost de Gouw, Timothy Bertram, Jonathan P. D. Abbatt, Nadine Borduas-Dedekind, and Dustin Poppendieck
Atmos. Meas. Tech., 18, 1013–1038, https://doi.org/10.5194/amt-18-1013-2025, https://doi.org/10.5194/amt-18-1013-2025, 2025
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Proton-transfer-reaction mass spectrometry (PTR-MS) is widely used for the measurement of volatile organic compounds (VOCs) both indoors and outdoors. An analytical challenge for PTR-MS measurements is the formation of unintended measurement interferences, product ion distributions (PIDs), that may appear in the data as VOCs of interest. We developed a method for quantifying PID formation and use interlaboratory comparison data to put quantitative constraints on PID formation.
Huan Yu, Isabelle De Smedt, Nicolas Theys, Maarten Sneep, Pepijn Veefkind, and Michel Van Roozendael
EGUsphere, https://doi.org/10.5194/egusphere-2025-478, https://doi.org/10.5194/egusphere-2025-478, 2025
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We introduce a new cloud retrieval algorithm using the O2-O2 absorption band at 477 nm to generate harmonized cloud datasets from OMI and TROPOMI. The algorithm improves upon the OMI O2-O2 operational cloud algorithm in several aspects. The new approach improves consistency in cloud parameters and NO2 retrievals between two sensors.
Arno Keppens, Daan Hubert, José Granville, Oindrila Nath, Jean-Christopher Lambert, Catherine Wespes, Pierre-François Coheur, Cathy Clerbaux, Anne Boynard, Richard Siddans, Barry Latter, Brian Kerridge, Serena Di Pede, Pepijn Veefkind, Juan Cuesta, Gaelle Dufour, Klaus-Peter Heue, Melanie Coldewey-Egbers, Diego Loyola, Andrea Orfanoz-Cheuquelaf, Swathi Maratt Satheesan, Kai-Uwe Eichmann, Alexei Rozanov, Viktoria F. Sofieva, Jerald R. Ziemke, Antje Inness, Roeland Van Malderen, and Lars Hoffmann
EGUsphere, https://doi.org/10.5194/egusphere-2024-3746, https://doi.org/10.5194/egusphere-2024-3746, 2025
This preprint is open for discussion and under review for Atmospheric Measurement Techniques (AMT).
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The first Tropospheric Ozone Assessment Report (TOAR) encountered discrepancies between several satellite sensors’ estimates of the distribution and change of ozone in the free troposphere. Therefore, contributing to the second TOAR, we harmonise as much as possible the observational perspective of sixteen tropospheric ozone products from satellites. This only partially accounts for the observed discrepancies, with a reduction of 10–40 % of the inter-product dispersion upon harmonisation.
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.
Mengyao Liu, Ronald van der A, Michiel van Weele, Lotte Bryan, Henk Eskes, Pepijn Veefkind, Yongxue Liu, Xiaojuan Lin, Jos de Laat, and Jieying Ding
Atmos. Meas. Tech., 17, 5261–5277, https://doi.org/10.5194/amt-17-5261-2024, https://doi.org/10.5194/amt-17-5261-2024, 2024
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A new divergence method was developed and applied to estimate methane emissions from TROPOMI observations over the Middle East, where it is typically challenging for a satellite to measure methane due to its complicated orography and surface albedo. Our results show the potential of TROPOMI to quantify methane emissions from various sources rather than big emitters from space after objectively excluding the artifacts in the retrieval.
Arno Keppens, Serena Di Pede, Daan Hubert, Jean-Christopher Lambert, Pepijn Veefkind, Maarten Sneep, Johan De Haan, Mark ter Linden, Thierry Leblanc, Steven Compernolle, Tijl Verhoelst, José Granville, Oindrila Nath, Ann Mari Fjæraa, Ian Boyd, Sander Niemeijer, Roeland Van Malderen, Herman G. J. Smit, Valentin Duflot, Sophie Godin-Beekmann, Bryan J. Johnson, Wolfgang Steinbrecht, David W. Tarasick, Debra E. Kollonige, Ryan M. Stauffer, Anne M. Thompson, Angelika Dehn, and Claus Zehner
Atmos. Meas. Tech., 17, 3969–3993, https://doi.org/10.5194/amt-17-3969-2024, https://doi.org/10.5194/amt-17-3969-2024, 2024
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The Sentinel-5P satellite operated by the European Space Agency has carried the TROPOspheric Monitoring Instrument (TROPOMI) around the Earth since October 2017. This mission also produces atmospheric ozone profile data which are described in detail for May 2018 to April 2023. Independent validation using ground-based reference measurements demonstrates that the operational ozone profile product mostly fully and at least partially complies with all mission requirements.
Adrianus de Laat, Jos van Geffen, Piet Stammes, Ronald van der A, Henk Eskes, and J. Pepijn Veefkind
Atmos. Chem. Phys., 24, 4511–4535, https://doi.org/10.5194/acp-24-4511-2024, https://doi.org/10.5194/acp-24-4511-2024, 2024
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Removal of stratospheric nitrogen oxides is crucial for the formation of the ozone hole. TROPOMI satellite measurements of nitrogen dioxide reveal the presence of a not dissimilar "nitrogen hole" that largely coincides with the ozone hole. Three very distinct regimes were identified: inside and outside the ozone hole and the transition zone in between. Our results introduce a valuable and innovative application highly relevant for Antarctic ozone hole and ozone layer recovery.
Melissa A. Morris, Demetrios Pagonis, Douglas A. Day, Joost A. de Gouw, Paul J. Ziemann, and Jose L. Jimenez
Atmos. Meas. Tech., 17, 1545–1559, https://doi.org/10.5194/amt-17-1545-2024, https://doi.org/10.5194/amt-17-1545-2024, 2024
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Polymer absorption of volatile organic compounds (VOCs) is important to characterize for atmospheric sampling setups (as interactions cause sampling delays) and indoor air quality. Here we test different polymer materials and quantify their absorptive capacities through modeling. We found the main polymers in carpets to be highly absorptive, acting as large reservoirs for indoor pollution. We also demonstrated how polymer tubes can be used as a low-cost gas separation technique.
Andrew R. Jensen, Abigail R. Koss, Ryder B. Hales, and Joost A. de Gouw
Atmos. Meas. Tech., 16, 5261–5285, https://doi.org/10.5194/amt-16-5261-2023, https://doi.org/10.5194/amt-16-5261-2023, 2023
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Quantification of a wide range of volatile organic compounds by proton-transfer-reaction mass spectrometry (PTR-MS) can be achieved with direct calibration of only a subset of compounds, characterization of instrument response, and simple reaction kinetics. We characterized our Vocus PTR-MS and developed a toolkit as a guide through this process. A catalytic zero air generator provided the lowest detection limits, and short, frequent calibrations informed variability in instrument response.
Kevin J. Nihill, Matthew M. Coggon, Christopher Y. Lim, Abigail R. Koss, Bin Yuan, Jordan E. Krechmer, Kanako Sekimoto, Jose L. Jimenez, Joost de Gouw, Christopher D. Cappa, Colette L. Heald, Carsten Warneke, and Jesse H. Kroll
Atmos. Chem. Phys., 23, 7887–7899, https://doi.org/10.5194/acp-23-7887-2023, https://doi.org/10.5194/acp-23-7887-2023, 2023
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In this work, we collect emissions from controlled burns of biomass fuels that can be found in the western United States into an environmental chamber in order to simulate their oxidation as they pass through the atmosphere. These findings provide a detailed characterization of the composition of the atmosphere downwind of wildfires. In turn, this will help to explore the effects of these changing emissions on downwind populations and will also directly inform atmospheric and climate models.
Konstantinos Michailidis, Maria-Elissavet Koukouli, Dimitris Balis, J. Pepijn Veefkind, Martin de Graaf, Lucia Mona, Nikolaos Papagianopoulos, Gesolmina Pappalardo, Ioanna Tsikoudi, Vassilis Amiridis, Eleni Marinou, Anna Gialitaki, Rodanthi-Elisavet Mamouri, Argyro Nisantzi, Daniele Bortoli, Maria João Costa, Vanda Salgueiro, Alexandros Papayannis, Maria Mylonaki, Lucas Alados-Arboledas, Salvatore Romano, Maria Rita Perrone, and Holger Baars
Atmos. Chem. Phys., 23, 1919–1940, https://doi.org/10.5194/acp-23-1919-2023, https://doi.org/10.5194/acp-23-1919-2023, 2023
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Comparisons with ground-based correlative lidar measurements constitute a key component in the validation of satellite aerosol products. This paper presents the validation of the TROPOMI aerosol layer height (ALH) product, using archived quality assured ground-based data from lidar stations that belong to the EARLINET network. Comparisons between the TROPOMI ALH and co-located EARLINET measurements show good agreement over the ocean.
John Douros, Henk Eskes, Jos van Geffen, K. Folkert Boersma, Steven Compernolle, Gaia Pinardi, Anne-Marlene Blechschmidt, Vincent-Henri Peuch, Augustin Colette, and Pepijn Veefkind
Geosci. Model Dev., 16, 509–534, https://doi.org/10.5194/gmd-16-509-2023, https://doi.org/10.5194/gmd-16-509-2023, 2023
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We focus on the challenges associated with comparing atmospheric composition models with satellite products such as tropospheric NO2 columns. The aim is to highlight the methodological difficulties and propose sound ways of doing such comparisons. Building on the comparisons, a new satellite product is proposed and made available, which takes advantage of higher-resolution, regional atmospheric modelling to improve estimates of troposheric NO2 columns over Europe.
Miriam Latsch, Andreas Richter, Henk Eskes, Maarten Sneep, Ping Wang, Pepijn Veefkind, Ronny Lutz, Diego Loyola, Athina Argyrouli, Pieter Valks, Thomas Wagner, Holger Sihler, Michel van Roozendael, Nicolas Theys, Huan Yu, Richard Siddans, and John P. Burrows
Atmos. Meas. Tech., 15, 6257–6283, https://doi.org/10.5194/amt-15-6257-2022, https://doi.org/10.5194/amt-15-6257-2022, 2022
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The article investigates different S5P TROPOMI cloud retrieval algorithms for tropospheric trace gas retrievals. The cloud products show differences primarily over snow and ice and for scenes under sun glint. Some issues regarding across-track dependence are found for the cloud fractions as well as for the cloud heights.
Johan F. de Haan, Ping Wang, Maarten Sneep, J. Pepijn Veefkind, and Piet Stammes
Geosci. Model Dev., 15, 7031–7050, https://doi.org/10.5194/gmd-15-7031-2022, https://doi.org/10.5194/gmd-15-7031-2022, 2022
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We present an overview of the DISAMAR radiative transfer code, highlighting the novel semi-analytical derivatives for the doubling–adding formulae and the new DISMAS technique for weak absorbers. DISAMAR includes forward simulations and retrievals for satellite spectral measurements from 270 to 2400 nm to determine instrument specifications for passive remote sensing. It has been used in various Sentinel-4/5P/5 projects and in the TROPOMI aerosol layer height and ozone profile products.
John T. Sullivan, Arnoud Apituley, Nora Mettig, Karin Kreher, K. Emma Knowland, Marc Allaart, Ankie Piters, Michel Van Roozendael, Pepijn Veefkind, Jerry R. Ziemke, Natalya Kramarova, Mark Weber, Alexei Rozanov, Laurence Twigg, Grant Sumnicht, and Thomas J. McGee
Atmos. Chem. Phys., 22, 11137–11153, https://doi.org/10.5194/acp-22-11137-2022, https://doi.org/10.5194/acp-22-11137-2022, 2022
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A TROPOspheric Monitoring Instrument (TROPOMI) validation campaign (TROLIX-19) was held in the Netherlands in September 2019. The research presented here focuses on using ozone lidars from NASA’s Goddard Space Flight Center to better evaluate the characterization of ozone throughout TROLIX-19 as compared to balloon-borne, space-borne and ground-based passive measurements, as well as a global coupled chemistry meteorology model.
Pieternel F. Levelt, Deborah C. Stein Zweers, Ilse Aben, Maite Bauwens, Tobias Borsdorff, Isabelle De Smedt, Henk J. Eskes, Christophe Lerot, Diego G. Loyola, Fabian Romahn, Trissevgeni Stavrakou, Nicolas Theys, Michel Van Roozendael, J. Pepijn Veefkind, and Tijl Verhoelst
Atmos. Chem. Phys., 22, 10319–10351, https://doi.org/10.5194/acp-22-10319-2022, https://doi.org/10.5194/acp-22-10319-2022, 2022
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Using the COVID-19 lockdown periods as an example, we show how Sentinel-5P/TROPOMI trace gas data (NO2, SO2, CO, HCHO and CHOCHO) can be used to understand impacts on air quality for regions and cities around the globe. We also provide information for both experienced and inexperienced users about how we created the data using state-of-the-art algorithms, where to get the data, methods taking meteorological and seasonal variability into consideration, and insights for future studies.
Quintus Kleipool, Nico Rozemeijer, Mirna van Hoek, Jonatan Leloux, Erwin Loots, Antje Ludewig, Emiel van der Plas, Daley Adrichem, Raoul Harel, Simon Spronk, Mark ter Linden, Glen Jaross, David Haffner, Pepijn Veefkind, and Pieternel F. Levelt
Atmos. Meas. Tech., 15, 3527–3553, https://doi.org/10.5194/amt-15-3527-2022, https://doi.org/10.5194/amt-15-3527-2022, 2022
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A new collection-4 dataset for the Ozone Monitoring Instrument (OMI) mission has been established to supersede the current collection-3 level-1b (L1b) data, produced with a newly developed L01b data processor based on the TROPOspheric Monitoring Instrument (TROPOMI) L01b processor. The collection-4 L1b data have a similar output format to the TROPOMI L1b data for easy connection of the data series. Many insights from the TROPOMI algorithms, as well as from OMI collection-3 usage, were included.
Nora Mettig, Mark Weber, Alexei Rozanov, John P. Burrows, Pepijn Veefkind, Anne M. Thompson, Ryan M. Stauffer, Thierry Leblanc, Gerard Ancellet, Michael J. Newchurch, Shi Kuang, Rigel Kivi, Matthew B. Tully, Roeland Van Malderen, Ankie Piters, Bogumil Kois, René Stübi, and Pavla Skrivankova
Atmos. Meas. Tech., 15, 2955–2978, https://doi.org/10.5194/amt-15-2955-2022, https://doi.org/10.5194/amt-15-2955-2022, 2022
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Vertical ozone profiles from combined spectral measurements in the UV and IR spectral ranges were retrieved by using data from TROPOMI/S5P and CrIS/Suomi-NPP. The vertical resolution and accuracy of the ozone profiles are improved by combining both wavelength ranges compared to retrievals limited to UV or IR spectral data only. The advancement of our TOPAS algorithm for combined measurements is required because in the UV-only retrieval the vertical resolution in the troposphere is very limited.
Kun Zhang, Zhiqiang Liu, Xiaojuan Zhang, Qing Li, Andrew Jensen, Wen Tan, Ling Huang, Yangjun Wang, Joost de Gouw, and Li Li
Atmos. Chem. Phys., 22, 4853–4866, https://doi.org/10.5194/acp-22-4853-2022, https://doi.org/10.5194/acp-22-4853-2022, 2022
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A significant increase in O3 concentrations was found during the lockdown period of COVID-19 in most areas of China. By field measurements coupled with machine learning, an observation-based model (OBM) and sensitivity analysis, we found the changes in the NOx / VOC ratio were a key reason for the significant rise in O3. To restrain O3 pollution, more efforts should be devoted to the control of anthropogenic OVOCs, alkenes and aromatics.
Jos van Geffen, Henk Eskes, Steven Compernolle, Gaia Pinardi, Tijl Verhoelst, Jean-Christopher Lambert, Maarten Sneep, Mark ter Linden, Antje Ludewig, K. Folkert Boersma, and J. Pepijn Veefkind
Atmos. Meas. Tech., 15, 2037–2060, https://doi.org/10.5194/amt-15-2037-2022, https://doi.org/10.5194/amt-15-2037-2022, 2022
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Nitrogen dioxide (NO2) is one of the main data products measured by the Tropospheric Monitoring Instrument (TROPOMI) on the Sentinel-5 Precursor (S5P) satellite. This study describes improvements in the TROPOMI NO2 retrieval leading to version v2.2, operational since 1 July 2021. It compares results with previous versions v1.2–v1.4 and with Ozone Monitoring Instrument (OMI) and ground-based measurements.
Daan Hubert, Klaus-Peter Heue, Jean-Christopher Lambert, Tijl Verhoelst, Marc Allaart, Steven Compernolle, Patrick D. Cullis, Angelika Dehn, Christian Félix, Bryan J. Johnson, Arno Keppens, Debra E. Kollonige, Christophe Lerot, Diego Loyola, Matakite Maata, Sukarni Mitro, Maznorizan Mohamad, Ankie Piters, Fabian Romahn, Henry B. Selkirk, Francisco R. da Silva, Ryan M. Stauffer, Anne M. Thompson, J. Pepijn Veefkind, Holger Vömel, Jacquelyn C. Witte, and Claus Zehner
Atmos. Meas. Tech., 14, 7405–7433, https://doi.org/10.5194/amt-14-7405-2021, https://doi.org/10.5194/amt-14-7405-2021, 2021
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We assess the first 2 years of TROPOMI tropical tropospheric ozone column data. Comparisons to reference measurements by ozonesonde and satellite sensors show that TROPOMI bias (−0.1 to +2.3 DU) and precision (1.5 to 2.5 DU) meet mission requirements. Potential causes of bias and its spatio-temporal structure are discussed, as well as ways to identify sampling errors. Our analysis of known geophysical patterns demonstrates the improved performance of TROPOMI with respect to its predecessors.
Nora Mettig, Mark Weber, Alexei Rozanov, Carlo Arosio, John P. Burrows, Pepijn Veefkind, Anne M. Thompson, Richard Querel, Thierry Leblanc, Sophie Godin-Beekmann, Rigel Kivi, and Matthew B. Tully
Atmos. Meas. Tech., 14, 6057–6082, https://doi.org/10.5194/amt-14-6057-2021, https://doi.org/10.5194/amt-14-6057-2021, 2021
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TROPOMI is a nadir-viewing satellite that has observed global atmospheric trace gases at unprecedented spatial resolution since 2017. The retrieval of ozone profiles with high accuracy has been demonstrated using the TOPAS (Tikhonov regularised Ozone Profile retrievAl with SCIATRAN) algorithm and applying appropriate spectral corrections to TROPOMI UV data. Ozone profiles from TROPOMI were compared to ozonesonde and lidar profiles, showing an agreement to within 5 % in the stratosphere.
Benjamin A. Nault, Duseong S. Jo, Brian C. McDonald, Pedro Campuzano-Jost, Douglas A. Day, Weiwei Hu, Jason C. Schroder, James Allan, Donald R. Blake, Manjula R. Canagaratna, Hugh Coe, Matthew M. Coggon, Peter F. DeCarlo, Glenn S. Diskin, Rachel Dunmore, Frank Flocke, Alan Fried, Jessica B. Gilman, Georgios Gkatzelis, Jacqui F. Hamilton, Thomas F. Hanisco, Patrick L. Hayes, Daven K. Henze, Alma Hodzic, James Hopkins, Min Hu, L. Greggory Huey, B. Thomas Jobson, William C. Kuster, Alastair Lewis, Meng Li, Jin Liao, M. Omar Nawaz, Ilana B. Pollack, Jeffrey Peischl, Bernhard Rappenglück, Claire E. Reeves, Dirk Richter, James M. Roberts, Thomas B. Ryerson, Min Shao, Jacob M. Sommers, James Walega, Carsten Warneke, Petter Weibring, Glenn M. Wolfe, Dominique E. Young, Bin Yuan, Qiang Zhang, Joost A. de Gouw, and Jose L. Jimenez
Atmos. Chem. Phys., 21, 11201–11224, https://doi.org/10.5194/acp-21-11201-2021, https://doi.org/10.5194/acp-21-11201-2021, 2021
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Secondary organic aerosol (SOA) is an important aspect of poor air quality for urban regions around the world, where a large fraction of the population lives. However, there is still large uncertainty in predicting SOA in urban regions. Here, we used data from 11 urban campaigns and show that the variability in SOA production in these regions is predictable and is explained by key emissions. These results are used to estimate the premature mortality associated with SOA in urban regions.
Frederik Tack, Alexis Merlaud, Marian-Daniel Iordache, Gaia Pinardi, Ermioni Dimitropoulou, Henk Eskes, Bart Bomans, Pepijn Veefkind, and Michel Van Roozendael
Atmos. Meas. Tech., 14, 615–646, https://doi.org/10.5194/amt-14-615-2021, https://doi.org/10.5194/amt-14-615-2021, 2021
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We assess the TROPOMI tropospheric NO2 product (OFFL v1.03.01; 3.5 km × 7 km at nadir observations) based on coinciding airborne APEX reference observations (~75 m × 120 m), acquired over polluted regions in Belgium. The TROPOMI NO2 product meets the mission requirements in terms of precision and accuracy. However, we show that TROPOMI is biased low over polluted areas, mainly due to the limited spatial resolution of a priori input for the AMF computation.
Tijl Verhoelst, Steven Compernolle, Gaia Pinardi, Jean-Christopher Lambert, Henk J. Eskes, Kai-Uwe Eichmann, Ann Mari Fjæraa, José Granville, Sander Niemeijer, Alexander Cede, Martin Tiefengraber, François Hendrick, Andrea Pazmiño, Alkiviadis Bais, Ariane Bazureau, K. Folkert Boersma, Kristof Bognar, Angelika Dehn, Sebastian Donner, Aleksandr Elokhov, Manuel Gebetsberger, Florence Goutail, Michel Grutter de la Mora, Aleksandr Gruzdev, Myrto Gratsea, Georg H. Hansen, Hitoshi Irie, Nis Jepsen, Yugo Kanaya, Dimitris Karagkiozidis, Rigel Kivi, Karin Kreher, Pieternel F. Levelt, Cheng Liu, Moritz Müller, Monica Navarro Comas, Ankie J. M. Piters, Jean-Pierre Pommereau, Thierry Portafaix, Cristina Prados-Roman, Olga Puentedura, Richard Querel, Julia Remmers, Andreas Richter, John Rimmer, Claudia Rivera Cárdenas, Lidia Saavedra de Miguel, Valery P. Sinyakov, Wolfgang Stremme, Kimberly Strong, Michel Van Roozendael, J. Pepijn Veefkind, Thomas Wagner, Folkard Wittrock, Margarita Yela González, and Claus Zehner
Atmos. Meas. Tech., 14, 481–510, https://doi.org/10.5194/amt-14-481-2021, https://doi.org/10.5194/amt-14-481-2021, 2021
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This paper reports on the ground-based validation of the NO2 data produced operationally by the TROPOMI instrument on board the Sentinel-5 Precursor satellite. Tropospheric, stratospheric, and total NO2 columns are compared to measurements collected from MAX-DOAS, ZSL-DOAS, and PGN/Pandora instruments respectively. The products are found to satisfy mission requirements in general, though negative mean differences are found at sites with high pollution levels. Potential causes are discussed.
Ivar R. van der Velde, Guido R. van der Werf, Sander Houweling, Henk J. Eskes, J. Pepijn Veefkind, Tobias Borsdorff, and Ilse Aben
Atmos. Chem. Phys., 21, 597–616, https://doi.org/10.5194/acp-21-597-2021, https://doi.org/10.5194/acp-21-597-2021, 2021
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This paper compares the relative atmospheric enhancements of CO and NO2 measured by the space-based instrument TROPOMI over different fire-prone ecosystems around the world. We find distinct spatial and temporal patterns in the ΔNO2 / ΔCO ratio that correspond to regional differences in combustion efficiency. This joint analysis provides a better understanding of regional-scale combustion characteristics and can help the fire modeling community to improve existing global emission inventories.
Megan S. Claflin, Demetrios Pagonis, Zachary Finewax, Anne V. Handschy, Douglas A. Day, Wyatt L. Brown, John T. Jayne, Douglas R. Worsnop, Jose L. Jimenez, Paul J. Ziemann, Joost de Gouw, and Brian M. Lerner
Atmos. Meas. Tech., 14, 133–152, https://doi.org/10.5194/amt-14-133-2021, https://doi.org/10.5194/amt-14-133-2021, 2021
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We have developed a field-deployable gas chromatograph with thermal desorption preconcentration and detector switching between two high-resolution mass spectrometers for in situ measurements of volatile organic compounds (VOCs). This system combines chromatography with both proton transfer and electron ionization to offer fast time response and continuous molecular speciation. This technique was applied during the 2018 ATHLETIC campaign to characterize VOC emissions in an indoor environment.
Maurits L. Kooreman, Piet Stammes, Victor Trees, Maarten Sneep, L. Gijsbert Tilstra, Martin de Graaf, Deborah C. Stein Zweers, Ping Wang, Olaf N. E. Tuinder, and J. Pepijn Veefkind
Atmos. Meas. Tech., 13, 6407–6426, https://doi.org/10.5194/amt-13-6407-2020, https://doi.org/10.5194/amt-13-6407-2020, 2020
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We investigated the influence of clouds on the Absorbing Aerosol Index (AAI), an indicator of the presence of small particles in the atmosphere. Clouds produce artifacts in AAI calculations on the individual measurement (7 km) scale, which was not seen with previous instruments, as well as on large (1000+ km) scales. To reduce these artefacts, we used three different AAI calculation techniques of varying complexity. We find that the AAI artifacts are reduced when using more complex techniques.
Laura M. Judd, Jassim A. Al-Saadi, James J. Szykman, Lukas C. Valin, Scott J. Janz, Matthew G. Kowalewski, Henk J. Eskes, J. Pepijn Veefkind, Alexander Cede, Moritz Mueller, Manuel Gebetsberger, Robert Swap, R. Bradley Pierce, Caroline R. Nowlan, Gonzalo González Abad, Amin Nehrir, and David Williams
Atmos. Meas. Tech., 13, 6113–6140, https://doi.org/10.5194/amt-13-6113-2020, https://doi.org/10.5194/amt-13-6113-2020, 2020
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This paper evaluates Sentinel-5P TROPOMI v1.2 NO2 tropospheric columns over New York City using data from airborne mapping spectrometers and a network of ground-based spectrometers (Pandora) collected in 2018. These evaluations consider impacts due to cloud parameters, a priori profile assumptions, and spatial and temporal variability. Overall, TROPOMI tropospheric NO2 columns appear to have a low bias in this region.
Aikaterini Bougiatioti, Athanasios Nenes, Jack J. Lin, Charles A. Brock, Joost A. de Gouw, Jin Liao, Ann M. Middlebrook, and André Welti
Atmos. Chem. Phys., 20, 12163–12176, https://doi.org/10.5194/acp-20-12163-2020, https://doi.org/10.5194/acp-20-12163-2020, 2020
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The number concentration of droplets in clouds in the summertime in the southeastern United States is influenced by aerosol variations but limited by the strong competition for supersaturated water vapor. Concurrent variations in vertical velocity magnify the response of cloud droplet number to aerosol increases by up to a factor of 5. Omitting the covariance of vertical velocity with aerosol number may therefore bias estimates of the cloud albedo effect from aerosols.
James M. Roberts, Chelsea E. Stockwell, Robert J. Yokelson, Joost de Gouw, Yong Liu, Vanessa Selimovic, Abigail R. Koss, Kanako Sekimoto, Matthew M. Coggon, Bin Yuan, Kyle J. Zarzana, Steven S. Brown, Cristina Santin, Stefan H. Doerr, and Carsten Warneke
Atmos. Chem. Phys., 20, 8807–8826, https://doi.org/10.5194/acp-20-8807-2020, https://doi.org/10.5194/acp-20-8807-2020, 2020
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We measured total reactive nitrogen, Nr, in lab fires from western North American fuels, along with measurements of individual nitrogen compounds. We measured the amount of N that gets converted to inactive compounds (avg. 70 %), and the amount that is accounted for by individual species (85 % of remaining N). We provide guidelines for how the reactive nitrogen is distributed among individual compounds such as NOx and ammonia. This will help estimates and predictions of wildfire emissions.
Christopher D. Cappa, Christopher Y. Lim, David H. Hagan, Matthew Coggon, Abigail Koss, Kanako Sekimoto, Joost de Gouw, Timothy B. Onasch, Carsten Warneke, and Jesse H. Kroll
Atmos. Chem. Phys., 20, 8511–8532, https://doi.org/10.5194/acp-20-8511-2020, https://doi.org/10.5194/acp-20-8511-2020, 2020
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Smoke from combustion of a wide range of biomass fuels (e.g., leaves, twigs, logs, peat, and dung) was photochemically aged in a small chamber for up to 8 d of equivalent atmospheric aging. Upon aging, the particle chemical composition and ability to absorb sunlight changed owing to reactions in both the gas and particulate phases. We developed a model to explain the observations and used this to derive insights into the aging of smoke in the atmosphere.
Antje Ludewig, Quintus Kleipool, Rolf Bartstra, Robin Landzaat, Jonatan Leloux, Erwin Loots, Peter Meijering, Emiel van der Plas, Nico Rozemeijer, Frank Vonk, and Pepijn Veefkind
Atmos. Meas. Tech., 13, 3561–3580, https://doi.org/10.5194/amt-13-3561-2020, https://doi.org/10.5194/amt-13-3561-2020, 2020
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After the Sentinel-5 Precursor satellite launch on 13 October 2017, its single payload, the TROPOspheric Monitoring Instrument (TROPOMI), was tested and calibrated extensively. Changes due to ageing of the instrument and new insights have led to updates to the L1b processor and its calibration key data, leading to improvements of the data quality. Regularly scheduled calibration measurements are used in the nominal operations phase (since 30 April 2018) to correct instrument degradation.
Swadhin Nanda, Martin de Graaf, J. Pepijn Veefkind, Maarten Sneep, Mark ter Linden, Jiyunting Sun, and Pieternel F. Levelt
Atmos. Meas. Tech., 13, 3043–3059, https://doi.org/10.5194/amt-13-3043-2020, https://doi.org/10.5194/amt-13-3043-2020, 2020
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This paper presents a first validation of the TROPOspheric Monitoring Instrument (TROPOMI) aerosol layer height (ALH) product, which is an estimate of the height of an aerosol layer using a spectrometer on board ESA's Sentinel-5 Precursor satellite mission. Comparison between the TROPOMI ALH product and co-located aerosol extinction heights from the CALIOP instrument on board NASA's CALIPSO mission show good agreement for selected cases over the ocean and large differences over land.
Debora Griffin, Christopher Sioris, Jack Chen, Nolan Dickson, Andrew Kovachik, Martin de Graaf, Swadhin Nanda, Pepijn Veefkind, Enrico Dammers, Chris A. McLinden, Paul Makar, and Ayodeji Akingunola
Atmos. Meas. Tech., 13, 1427–1445, https://doi.org/10.5194/amt-13-1427-2020, https://doi.org/10.5194/amt-13-1427-2020, 2020
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This study looks into validating the aerosol layer height product from the recently launched TROPOspheric Monitoring Instrument (TROPOMI) for forest fire plume through comparisons with two other satellite products, and interpreting differences due to the individual measurement techniques. These satellite observations are compared to predicted plume heights from Environment and Climate Change's air quality forecast model.
Jos van Geffen, K. Folkert Boersma, Henk Eskes, Maarten Sneep, Mark ter Linden, Marina Zara, and J. Pepijn Veefkind
Atmos. Meas. Tech., 13, 1315–1335, https://doi.org/10.5194/amt-13-1315-2020, https://doi.org/10.5194/amt-13-1315-2020, 2020
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The Tropospheric Monitoring Instrument (TROPOMI) provides atmospheric trace gase and cloud and aerosol property measurements at unprecedented spatial resolution. This study focusses on the TROPOMI NO2 slant column density (SCD) retrieval: the retrieval method used, the stability of and uncertainties in the SCDs, and a comparison with Ozone Monitoring Instrument (OMI) NO2 SCDs. TROPOMI shows a superior performance compared to OMI/QA4ECV and operates as anticipated from instrument specifications.
Jiyunting Sun, J. Pepijn Veefkind, Peter van Velthoven, L. Gijsbert Tilstra, Julien Chimot, Swadhin Nanda, and Pieternel F. Levelt
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2020-39, https://doi.org/10.5194/acp-2020-39, 2020
Revised manuscript not accepted
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ALH is one of the major concerns in quantifying aerosol absorption from the ultra-violet aerosol index (UVAI). The UVAI has a global daily record since 1978, whereas a corresponding ALH data set is limited. In this paper, we attempt to construct a global long-term ALH data set derived from the MERRA-2 aerosol fields that can be favorable in interpreting aerosol absorption from UVAI. We also give comments on several satellite ALH products in terms of the UVAI altitude dependence.
Samuel Quesada-Ruiz, Jean-Luc Attié, William A. Lahoz, Rachid Abida, Philippe Ricaud, Laaziz El Amraoui, Régina Zbinden, Andrea Piacentini, Mathieu Joly, Henk Eskes, Arjo Segers, Lyana Curier, Johan de Haan, Jukka Kujanpää, Albert Christiaan Plechelmus Oude Nijhuis, Johanna Tamminen, Renske Timmermans, and Pepijn Veefkind
Atmos. Meas. Tech., 13, 131–152, https://doi.org/10.5194/amt-13-131-2020, https://doi.org/10.5194/amt-13-131-2020, 2020
Swadhin Nanda, Martin de Graaf, J. Pepijn Veefkind, Mark ter Linden, Maarten Sneep, Johan de Haan, and Pieternel F. Levelt
Atmos. Meas. Tech., 12, 6619–6634, https://doi.org/10.5194/amt-12-6619-2019, https://doi.org/10.5194/amt-12-6619-2019, 2019
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This paper discusses a neural network forward model used by the operational aerosol layer height (ALH) retrieval algorithm for the TROPOspheric Monitoring Instrument (TROPOMI) on board the European Sentinel-5 Precursor satellite mission. This model replaces online radiative transfer calculations within the oxygen A-band, improving the speed of the algorithm by 3 orders of magnitude. With this advancement in the algorithm's speed, TROPOMI is set to deliver the ALH product operationally.
Matthew M. Coggon, Christopher Y. Lim, Abigail R. Koss, Kanako Sekimoto, Bin Yuan, Jessica B. Gilman, David H. Hagan, Vanessa Selimovic, Kyle J. Zarzana, Steven S. Brown, James M. Roberts, Markus Müller, Robert Yokelson, Armin Wisthaler, Jordan E. Krechmer, Jose L. Jimenez, Christopher Cappa, Jesse H. Kroll, Joost de Gouw, and Carsten Warneke
Atmos. Chem. Phys., 19, 14875–14899, https://doi.org/10.5194/acp-19-14875-2019, https://doi.org/10.5194/acp-19-14875-2019, 2019
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Wildfire emissions significantly contribute to adverse air quality; however, the chemical processes that lead to hazardous pollutants, such as ozone, are not fully understood. In this study, we describe laboratory experiments where we simulate the atmospheric chemistry of smoke emitted from a range of biomass fuels. We show that certain understudied compounds, such as furans and phenolic compounds, are significant contributors to pollutants formed as a result of typical atmospheric oxidation.
Jiyunting Sun, Pepijn Veefkind, Swadhin Nanda, Peter van Velthoven, and Pieternel Levelt
Atmos. Meas. Tech., 12, 6319–6340, https://doi.org/10.5194/amt-12-6319-2019, https://doi.org/10.5194/amt-12-6319-2019, 2019
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Single scattering albedo (SSA) is critical for reducing uncertainties in radiative forcing assessment. This paper presents two methods to retrieve SSA from satellite observations of the near-UV absorbing aerosol index (UVAI). The first is physically based radiative transfer simulations; the second is a statistically based machine learning algorithm. The result of the latter is encouraging. Both methods show that the ALH is necessary to quantitatively interpret aerosol absorption from UVAI.
Renske Timmermans, Arjo Segers, Lyana Curier, Rachid Abida, Jean-Luc Attié, Laaziz El Amraoui, Henk Eskes, Johan de Haan, Jukka Kujanpää, William Lahoz, Albert Oude Nijhuis, Samuel Quesada-Ruiz, Philippe Ricaud, Pepijn Veefkind, and Martijn Schaap
Atmos. Chem. Phys., 19, 12811–12833, https://doi.org/10.5194/acp-19-12811-2019, https://doi.org/10.5194/acp-19-12811-2019, 2019
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We present an evaluation of the added value of the Sentinel-4 and Sentinel-5P missions for air quality analyses of NO2. For this, synthetic observations for both missions are generated and combined with a chemistry transport model. While hourly Sentinel-4 NO2 observations over Europe benefit modelled NO2 analyses throughout the entire day, daily Sentinel-5P NO2 observations with global coverage show an impact up to 3–6 h after overpass. This supports the need for a combination of missions.
Christopher Y. Lim, David H. Hagan, Matthew M. Coggon, Abigail R. Koss, Kanako Sekimoto, Joost de Gouw, Carsten Warneke, Christopher D. Cappa, and Jesse H. Kroll
Atmos. Chem. Phys., 19, 12797–12809, https://doi.org/10.5194/acp-19-12797-2019, https://doi.org/10.5194/acp-19-12797-2019, 2019
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Wildfires are a large source of gases and particles to the atmosphere, both of which impact human health and climate. The amount and composition of particles from wildfires can change with time in the atmosphere; however, the impact of aging is not well understood. In a series of controlled laboratory experiments, we show that the particles are oxidized and a significant fraction of the gas-phase carbon (24 %–56 %) is converted to particle mass over the course of several days in the atmosphere.
Xin Chen, Dylan B. Millet, Hanwant B. Singh, Armin Wisthaler, Eric C. Apel, Elliot L. Atlas, Donald R. Blake, Ilann Bourgeois, Steven S. Brown, John D. Crounse, Joost A. de Gouw, Frank M. Flocke, Alan Fried, Brian G. Heikes, Rebecca S. Hornbrook, Tomas Mikoviny, Kyung-Eun Min, Markus Müller, J. Andrew Neuman, Daniel W. O'Sullivan, Jeff Peischl, Gabriele G. Pfister, Dirk Richter, James M. Roberts, Thomas B. Ryerson, Stephen R. Shertz, Chelsea R. Thompson, Victoria Treadaway, Patrick R. Veres, James Walega, Carsten Warneke, Rebecca A. Washenfelder, Petter Weibring, and Bin Yuan
Atmos. Chem. Phys., 19, 9097–9123, https://doi.org/10.5194/acp-19-9097-2019, https://doi.org/10.5194/acp-19-9097-2019, 2019
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Volatile organic compounds (VOCs) affect air quality and modify the lifetimes of other pollutants. We combine a high-resolution 3-D atmospheric model with an ensemble of aircraft observations to perform an integrated analysis of the VOC budget over North America. We find that biogenic emissions provide the main source of VOC reactivity even in most major cities. Our findings point to key gaps in current models related to oxygenated VOCs and to the distribution of VOCs in the free troposphere.
Benjamin L. Deming, Demetrios Pagonis, Xiaoxi Liu, Douglas A. Day, Ranajit Talukdar, Jordan E. Krechmer, Joost A. de Gouw, Jose L. Jimenez, and Paul J. Ziemann
Atmos. Meas. Tech., 12, 3453–3461, https://doi.org/10.5194/amt-12-3453-2019, https://doi.org/10.5194/amt-12-3453-2019, 2019
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Losses or measurement delays of gas-phase compounds sampled through tubing are important to atmospheric science. Here we characterize 14 tubing materials by measuring the effects on step changes in organic compound concentration. We find that polymeric tubings exhibit absorptive partitioning behaviour while glass and metal tubings show adsorptive partitioning. Adsorptive materials impart complex humidity, concentration, and VOC–VOC interaction dependencies that absorptive tubings do not.
Xiaoxi Liu, Benjamin Deming, Demetrios Pagonis, Douglas A. Day, Brett B. Palm, Ranajit Talukdar, James M. Roberts, Patrick R. Veres, Jordan E. Krechmer, Joel A. Thornton, Joost A. de Gouw, Paul J. Ziemann, and Jose L. Jimenez
Atmos. Meas. Tech., 12, 3137–3149, https://doi.org/10.5194/amt-12-3137-2019, https://doi.org/10.5194/amt-12-3137-2019, 2019
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Delays or losses of gases in sampling tubing and instrumental surfaces due to surface interactions can lead to inaccurate quantification. By sampling with several chemical ionization mass spectrometers and six tubing materials, we quantify delays of semivolatile organic compounds and small polar gases. Delay times generally increase with decreasing volatility or increasing polarity and also depend on materials. The method and results will inform inlet material selection and instrumental design.
Shino Toma, Steve Bertman, Christopher Groff, Fulizi Xiong, Paul B. Shepson, Paul Romer, Kaitlin Duffey, Paul Wooldridge, Ronald Cohen, Karsten Baumann, Eric Edgerton, Abigail R. Koss, Joost de Gouw, Allen Goldstein, Weiwei Hu, and Jose L. Jimenez
Atmos. Chem. Phys., 19, 1867–1880, https://doi.org/10.5194/acp-19-1867-2019, https://doi.org/10.5194/acp-19-1867-2019, 2019
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Acyl peroxy nitrates (APN) were measured near the ground in Alabama using GC in summer 2013 to study biosphere–atmosphere interactions. APN were lower than measured in the SE USA over the past 2 decades. Historical data showed APN in 2013 was limited by NOx and production was dominated by biogenic precursors more than in the past. Isoprene-derived MPAN correlated with isoprene hydroxynitrates as NOx-dependent products. MPAN varied with aerosol growth, but not with N-containing particles.
Julien Chimot, J. Pepijn Veefkind, Johan F. de Haan, Piet Stammes, and Pieternel F. Levelt
Atmos. Meas. Tech., 12, 491–516, https://doi.org/10.5194/amt-12-491-2019, https://doi.org/10.5194/amt-12-491-2019, 2019
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The reference OMI tropospheric NO2 product was reprocessed by new aerosol correction parameters retrieved from the 477 nm O2–O2 band over eastern China and South America for 2 years. These new parameters are from different and separate algorithms, allowing improved use of the 477 nm O2–O2 band. All the tested approaches improve the aerosol correction in the OMI tropospheric NO2 product. We demonstrate the possibility of applying an explicit aerosol correction based on the 477 nm O2–O2 band.
Benjamin A. Nault, Pedro Campuzano-Jost, Douglas A. Day, Jason C. Schroder, Bruce Anderson, Andreas J. Beyersdorf, Donald R. Blake, William H. Brune, Yonghoon Choi, Chelsea A. Corr, Joost A. de Gouw, Jack Dibb, Joshua P. DiGangi, Glenn S. Diskin, Alan Fried, L. Gregory Huey, Michelle J. Kim, Christoph J. Knote, Kara D. Lamb, Taehyoung Lee, Taehyun Park, Sally E. Pusede, Eric Scheuer, Kenneth L. Thornhill, Jung-Hun Woo, and Jose L. Jimenez
Atmos. Chem. Phys., 18, 17769–17800, https://doi.org/10.5194/acp-18-17769-2018, https://doi.org/10.5194/acp-18-17769-2018, 2018
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Aerosol impacts visibility and human health in large cities. Sources of aerosols are still highly uncertain, especially for cities surrounded by numerous other cities. We use observations collected during the Korea–United States Air Quality study to determine sources of organic aerosol (OA). We find that secondary OA (SOA) is rapidly produced over Seoul, South Korea, and that the sources of the SOA originate from short-lived hydrocarbons, which originate from local emissions.
Quintus Kleipool, Antje Ludewig, Ljubiša Babić, Rolf Bartstra, Remco Braak, Werner Dierssen, Pieter-Jan Dewitte, Pepijn Kenter, Robin Landzaat, Jonatan Leloux, Erwin Loots, Peter Meijering, Emiel van der Plas, Nico Rozemeijer, Dinand Schepers, Daniel Schiavini, Joost Smeets, Giuseppe Vacanti, Frank Vonk, and Pepijn Veefkind
Atmos. Meas. Tech., 11, 6439–6479, https://doi.org/10.5194/amt-11-6439-2018, https://doi.org/10.5194/amt-11-6439-2018, 2018
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This paper reports on the pre-launch calibration of the TROPOMI instrument on board ESA's Sentinel 5P satellite. This calibration is needed to convert the raw instrument digital data to physical quantities like Earth radiance and Sun irradiance. From these quantities atmospheric properties can be derived. The paper shows that the chosen approach to calibration and analysis was successful and that
the achieved accuracy makes high-quality observations of the Earth's atmosphere feasible.
Kyle J. Zarzana, Vanessa Selimovic, Abigail R. Koss, Kanako Sekimoto, Matthew M. Coggon, Bin Yuan, William P. Dubé, Robert J. Yokelson, Carsten Warneke, Joost A. de Gouw, James M. Roberts, and Steven S. Brown
Atmos. Chem. Phys., 18, 15451–15470, https://doi.org/10.5194/acp-18-15451-2018, https://doi.org/10.5194/acp-18-15451-2018, 2018
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Emissions of glyoxal and methylglyoxal from fuels common to the western United States were measured using cavity-enhanced spectroscopy, which provides a more selective measurement of those compounds than was previously available. Primary emissions of glyoxal were lower than previously reported and showed variability between the different fuel groups. However, emissions of glyoxal relative to formaldehyde were constant across almost all the fuel groups at 6 %–7 %.
Jiyunting Sun, J. Pepijn Veefkind, Peter van Velthoven, and Pieternel F. Levelt
Atmos. Meas. Tech., 11, 5261–5277, https://doi.org/10.5194/amt-11-5261-2018, https://doi.org/10.5194/amt-11-5261-2018, 2018
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Near-UV AAI is a qualitative parameter detecting the elevated absorbing aerosol layer. A long-term AAI record of satellite observations has the potential to quantify aerosol absorption on a global scale. Our study presents the possibility of retrieving single-scattering albedo with OMI-measured AAI. The comparison with AERONET is satisfactory and further research will be on how the aerosol wavelength-dependent refractive index and aerosol profile affect the quantification of aerosol absorption.
Juliane L. Fry, Steven S. Brown, Ann M. Middlebrook, Peter M. Edwards, Pedro Campuzano-Jost, Douglas A. Day, José L. Jimenez, Hannah M. Allen, Thomas B. Ryerson, Ilana Pollack, Martin Graus, Carsten Warneke, Joost A. de Gouw, Charles A. Brock, Jessica Gilman, Brian M. Lerner, William P. Dubé, Jin Liao, and André Welti
Atmos. Chem. Phys., 18, 11663–11682, https://doi.org/10.5194/acp-18-11663-2018, https://doi.org/10.5194/acp-18-11663-2018, 2018
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This paper uses measurements made during research aircraft flights through power plant smokestack emissions plumes as a natural laboratory in the field experiment. We investigated a specific source of airborne particulate matter from the combination of human-produced NOx pollutant emissions (the smokestack plumes) with isoprene emitted by naturally by trees in the southeastern United States. These field-based yields appear to be higher than those typically measured in chamber studies.
Kanako Sekimoto, Abigail R. Koss, Jessica B. Gilman, Vanessa Selimovic, Matthew M. Coggon, Kyle J. Zarzana, Bin Yuan, Brian M. Lerner, Steven S. Brown, Carsten Warneke, Robert J. Yokelson, James M. Roberts, and Joost de Gouw
Atmos. Chem. Phys., 18, 9263–9281, https://doi.org/10.5194/acp-18-9263-2018, https://doi.org/10.5194/acp-18-9263-2018, 2018
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We found that on average 85 % of the VOC emissions from biomass burning across various fuels representative of the western US (including various coniferous and chaparral fuels) can be explained using only two emission profiles: (i) a high-temperature pyrolysis profile and (ii) a low-temperature pyrolysis profile. The high-temperature profile is quantitatively similar between different fuel types (r2 > 0.84), and likewise for the low-temperature profile.
Swadhin Nanda, J. Pepijn Veefkind, Martin de Graaf, Maarten Sneep, Piet Stammes, Johan F. de Haan, Abram F. J. Sanders, Arnoud Apituley, Olaf Tuinder, and Pieternel F. Levelt
Atmos. Meas. Tech., 11, 3263–3280, https://doi.org/10.5194/amt-11-3263-2018, https://doi.org/10.5194/amt-11-3263-2018, 2018
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An approach to estimate the height of aerosol plumes over land from satellite measurements of the oxygen A band is proposed. The method, termed dynamic scaling, forces the retrieval to use spectral points that contain more height information. The method is tested in a synthetic environment as well as with GOME-2A and GOME-2B measurements of wildfire plumes over Europe, with very encouraging results. This method can be easily applied to other aerosol height algorithms using least squares.
Si-Wan Kim, Vijay Natraj, Seoyoung Lee, Hyeong-Ahn Kwon, Rokjin Park, Joost de Gouw, Gregory Frost, Jhoon Kim, Jochen Stutz, Michael Trainer, Catalina Tsai, and Carsten Warneke
Atmos. Chem. Phys., 18, 7639–7655, https://doi.org/10.5194/acp-18-7639-2018, https://doi.org/10.5194/acp-18-7639-2018, 2018
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Formaldehyde (HCHO) is a hazardous air pollutant and is associated with tropospheric ozone production. HCHO has been monitored from space. In this study, to acquire high-quality satellite-based HCHO observations, we utilize fine-resolution atmospheric chemistry model results as an input to the computer code for satellite retrievals over the Los Angeles Basin. Our study indicates that the use of fine-resolution profile shapes helps to identify HCHO plumes from space.
Arve Kylling, Sophie Vandenbussche, Virginie Capelle, Juan Cuesta, Lars Klüser, Luca Lelli, Thomas Popp, Kerstin Stebel, and Pepijn Veefkind
Atmos. Meas. Tech., 11, 2911–2936, https://doi.org/10.5194/amt-11-2911-2018, https://doi.org/10.5194/amt-11-2911-2018, 2018
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The aerosol layer height is one of four aerosol parameters which is needed to enhance our understanding of aerosols' role in the climate system. Both active and passive measurement methods may be used to estimate the aerosol layer height. Aerosol height estimates made from passive infrared and solar satellite sensors measurements are compared with satellite-borne lidar estimates. There is considerable variation between the retrieved dust heights and how they compare with the lidar.
Isabelle De Smedt, Nicolas Theys, Huan Yu, Thomas Danckaert, Christophe Lerot, Steven Compernolle, Michel Van Roozendael, Andreas Richter, Andreas Hilboll, Enno Peters, Mattia Pedergnana, Diego Loyola, Steffen Beirle, Thomas Wagner, Henk Eskes, Jos van Geffen, Klaas Folkert Boersma, and Pepijn Veefkind
Atmos. Meas. Tech., 11, 2395–2426, https://doi.org/10.5194/amt-11-2395-2018, https://doi.org/10.5194/amt-11-2395-2018, 2018
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This paper introduces the formaldehyde (HCHO) tropospheric vertical column retrieval algorithm implemented in the TROPOMI/Sentinel-5 Precursor operational processor, and comprehensively describes its various retrieval steps. Furthermore, algorithmic improvements developed in the framework of the EU FP7-project QA4ECV are described for future updates of the processor. Detailed error estimates are discussed in the light of Copernicus user requirements and needs for validation are highlighted.
Pieternel F. Levelt, Joanna Joiner, Johanna Tamminen, J. Pepijn Veefkind, Pawan K. Bhartia, Deborah C. Stein Zweers, Bryan N. Duncan, David G. Streets, Henk Eskes, Ronald van der A, Chris McLinden, Vitali Fioletov, Simon Carn, Jos de Laat, Matthew DeLand, Sergey Marchenko, Richard McPeters, Jerald Ziemke, Dejian Fu, Xiong Liu, Kenneth Pickering, Arnoud Apituley, Gonzalo González Abad, Antti Arola, Folkert Boersma, Christopher Chan Miller, Kelly Chance, Martin de Graaf, Janne Hakkarainen, Seppo Hassinen, Iolanda Ialongo, Quintus Kleipool, Nickolay Krotkov, Can Li, Lok Lamsal, Paul Newman, Caroline Nowlan, Raid Suleiman, Lieuwe Gijsbert Tilstra, Omar Torres, Huiqun Wang, and Krzysztof Wargan
Atmos. Chem. Phys., 18, 5699–5745, https://doi.org/10.5194/acp-18-5699-2018, https://doi.org/10.5194/acp-18-5699-2018, 2018
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The aim of this paper is to highlight the many successes of the Ozone Monitoring Instrument (OMI) spanning more than 13 years. Data from OMI have been used in a wide range of applications. Due to its unprecedented spatial resolution, in combination with daily global coverage, OMI plays a unique role in measuring trace gases important for the ozone layer, air quality, and climate change. OMI data continue to be used for new research and applications.
Julien Chimot, J. Pepijn Veefkind, Tim Vlemmix, and Pieternel F. Levelt
Atmos. Meas. Tech., 11, 2257–2277, https://doi.org/10.5194/amt-11-2257-2018, https://doi.org/10.5194/amt-11-2257-2018, 2018
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Aerosol layer height (ALH) was retrieved from the OMI 477 nm O2–O2 band and its spatial pattern evaluated over selected cloud-free scenes. We used a neural network approach previously trained and developed. Comparison with CALIOP aerosol level 2 products over urban and industrial pollution in east China shows consistent spatial patterns. In addition, we show the possibility to determine the height of thick aerosol layers released by intensive biomass burning events in South America and Russia.
Abigail R. Koss, Kanako Sekimoto, Jessica B. Gilman, Vanessa Selimovic, Matthew M. Coggon, Kyle J. Zarzana, Bin Yuan, Brian M. Lerner, Steven S. Brown, Jose L. Jimenez, Jordan Krechmer, James M. Roberts, Carsten Warneke, Robert J. Yokelson, and Joost de Gouw
Atmos. Chem. Phys., 18, 3299–3319, https://doi.org/10.5194/acp-18-3299-2018, https://doi.org/10.5194/acp-18-3299-2018, 2018
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Non-methane organic gases (NMOGs) were detected by proton-transfer-reaction mass spectrometry (PTR-ToF) during an extensive laboratory characterization of wildfire emissions. Identifications for PTR-ToF ion masses are proposed and supported by a combination of techniques. Overall excellent agreement with other instrumentation is shown. Scalable emission factors and ratios are reported for many newly reported reactive species. An analysis of chemical characteristics is presented.
Vanessa Selimovic, Robert J. Yokelson, Carsten Warneke, James M. Roberts, Joost de Gouw, James Reardon, and David W. T. Griffith
Atmos. Chem. Phys., 18, 2929–2948, https://doi.org/10.5194/acp-18-2929-2018, https://doi.org/10.5194/acp-18-2929-2018, 2018
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We burned fuels representing western US wildfires in large-scale laboratory simulations to generate relevant emissions as confirmed by lab–field comparison. We report emission factors (EFs) for light scattering and absorption and BC along with SSA at 870 and 401 nm and AAE. We report EF for 22 trace gases that are major inorganic and organic emissions from flaming and smoldering. We report trace gas EF for species rarely (NH3) or not yet measured (e.g., HONO, acetic acid) for real US wildfires.
Jingqiu Mao, Annmarie Carlton, Ronald C. Cohen, William H. Brune, Steven S. Brown, Glenn M. Wolfe, Jose L. Jimenez, Havala O. T. Pye, Nga Lee Ng, Lu Xu, V. Faye McNeill, Kostas Tsigaridis, Brian C. McDonald, Carsten Warneke, Alex Guenther, Matthew J. Alvarado, Joost de Gouw, Loretta J. Mickley, Eric M. Leibensperger, Rohit Mathur, Christopher G. Nolte, Robert W. Portmann, Nadine Unger, Mika Tosca, and Larry W. Horowitz
Atmos. Chem. Phys., 18, 2615–2651, https://doi.org/10.5194/acp-18-2615-2018, https://doi.org/10.5194/acp-18-2615-2018, 2018
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This paper is aimed at discussing progress in evaluating, diagnosing, and improving air quality and climate modeling using comparisons to SAS observations as a guide to thinking about improvements to mechanisms and parameterizations in models.
Paul S. Romer, Kaitlin C. Duffey, Paul J. Wooldridge, Eric Edgerton, Karsten Baumann, Philip A. Feiner, David O. Miller, William H. Brune, Abigail R. Koss, Joost A. de Gouw, Pawel K. Misztal, Allen H. Goldstein, and Ronald C. Cohen
Atmos. Chem. Phys., 18, 2601–2614, https://doi.org/10.5194/acp-18-2601-2018, https://doi.org/10.5194/acp-18-2601-2018, 2018
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Observations of increased ozone on hotter days are widely reported, but the mechanisms driving this relationship remain uncertain. We use measurements from the rural southeastern United States to study how temperature affects ozone production. We find that changing NOx emissions, most likely from soil microbes, can be a major driver of increased ozone with temperature in the continental background. These findings suggest that ozone will increase with temperature under a wide range of conditions.
Catalina Tsai, Max Spolaor, Santo Fedele Colosimo, Olga Pikelnaya, Ross Cheung, Eric Williams, Jessica B. Gilman, Brian M. Lerner, Robert J. Zamora, Carsten Warneke, James M. Roberts, Ravan Ahmadov, Joost de Gouw, Timothy Bates, Patricia K. Quinn, and Jochen Stutz
Atmos. Chem. Phys., 18, 1977–1996, https://doi.org/10.5194/acp-18-1977-2018, https://doi.org/10.5194/acp-18-1977-2018, 2018
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Nitrous acid (HONO) photolysis is an important source of hydroxyl radicals (OH). Vertical HONO fluxes, observed in the snow-free, wintertime Uintah Basin, Utah, USA, show that chemical formation of HONO on the ground closes the HONO budget. Under high NOx conditions, HONO formation is most likely due to photo-enhanced conversion of NO2 on the ground. Under moderate to low NO2 conditions, photolysis of HNO3 on the ground seems to be the most likely source of HONO.
Swadhin Nanda, Martin de Graaf, Maarten Sneep, Johan F. de Haan, Piet Stammes, Abram F. J. Sanders, Olaf Tuinder, J. Pepijn Veefkind, and Pieternel F. Levelt
Atmos. Meas. Tech., 11, 161–175, https://doi.org/10.5194/amt-11-161-2018, https://doi.org/10.5194/amt-11-161-2018, 2018
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Estimating aerosol layer height in the atmosphere from satellite data in the oxygen A band (758–770 nm) over land is challenging over land, since the surface is generally very bright in this wavelength region. This paper discusses an interplay between the surface and the atmosphere in their contributions to the top-of-atmosphere reflectance spectrum and the consequent biases obtained while estimating aerosol layer height, using synthetic data and real data from the GOME-2 satellite instrument.
Theodore K. Koenig, Rainer Volkamer, Sunil Baidar, Barbara Dix, Siyuan Wang, Daniel C. Anderson, Ross J. Salawitch, Pamela A. Wales, Carlos A. Cuevas, Rafael P. Fernandez, Alfonso Saiz-Lopez, Mathew J. Evans, Tomás Sherwen, Daniel J. Jacob, Johan Schmidt, Douglas Kinnison, Jean-François Lamarque, Eric C. Apel, James C. Bresch, Teresa Campos, Frank M. Flocke, Samuel R. Hall, Shawn B. Honomichl, Rebecca Hornbrook, Jørgen B. Jensen, Richard Lueb, Denise D. Montzka, Laura L. Pan, J. Michael Reeves, Sue M. Schauffler, Kirk Ullmann, Andrew J. Weinheimer, Elliot L. Atlas, Valeria Donets, Maria A. Navarro, Daniel Riemer, Nicola J. Blake, Dexian Chen, L. Gregory Huey, David J. Tanner, Thomas F. Hanisco, and Glenn M. Wolfe
Atmos. Chem. Phys., 17, 15245–15270, https://doi.org/10.5194/acp-17-15245-2017, https://doi.org/10.5194/acp-17-15245-2017, 2017
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Tropospheric inorganic bromine (BrO and Bry) shows a C-shaped profile over the tropical western Pacific Ocean, and supports previous speculation that marine convection is a source for inorganic bromine from sea salt to the upper troposphere. The Bry profile in the tropical tropopause layer (TTL) is complex, suggesting that the total Bry budget in the TTL is not closed without considering aerosol bromide. The implications for atmospheric composition and bromine sources are discussed.
Demetrios Pagonis, Jordan E. Krechmer, Joost de Gouw, Jose L. Jimenez, and Paul J. Ziemann
Atmos. Meas. Tech., 10, 4687–4696, https://doi.org/10.5194/amt-10-4687-2017, https://doi.org/10.5194/amt-10-4687-2017, 2017
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Laboratory studies were conducted to investigate gas-wall partitioning of atmospheric organic compounds in Teflon tubing and inside an instrument used to monitor concentrations. Rapid partitioning caused time delays in instrument response that vary with tubing length and diameter, flow rate, and compound volatility. Tubing delay times of seconds to hours were described using a model that also included effects of instrument surfaces. The results can enable better design of air sampling systems.
Robert C. Rhew, Malte Julian Deventer, Andrew A. Turnipseed, Carsten Warneke, John Ortega, Steve Shen, Luis Martinez, Abigail Koss, Brian M. Lerner, Jessica B. Gilman, James N. Smith, Alex B. Guenther, and Joost A. de Gouw
Atmos. Chem. Phys., 17, 13417–13438, https://doi.org/10.5194/acp-17-13417-2017, https://doi.org/10.5194/acp-17-13417-2017, 2017
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Alkenes emanate from both natural and anthropogenic sources and can contribute to atmospheric ozone production. This study measured
lightalkene (ethene, propene and butene) fluxes from a ponderosa pine forest using a novel relaxed eddy accumulation method, revealing much larger emissions than previously estimated and accounting for a significant fraction of OH reactivity. Emissions have a diurnal cycle related to sunlight and temperature, and the forest canopy appears to be the source.
Tim Vlemmix, Xinrui (Jerry) Ge, Bryan T. G. de Goeij, Len F. van der Wal, Gerard C. J. Otter, Piet Stammes, Ping Wang, Alexis Merlaud, Dirk Schüttemeyer, Andreas C. Meier, J. Pepijn Veefkind, and Pieternel F. Levelt
Atmos. Meas. Tech. Discuss., https://doi.org/10.5194/amt-2017-257, https://doi.org/10.5194/amt-2017-257, 2017
Revised manuscript has not been submitted
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We present a first analysis of UV/VIS spectral measurements obtained with the Spectrolite Breadboard Instrument (developed by TNO, The Netherlands) during the AROMAPEX campaign held in Berlin in April 2016 (campaign supported by ESA and EUFAR). This new sensor was used to measure air pollution in the form of tropospheric NO2 columns. The study focuses specifically on the retrieval of surface reflectances, an important intermediate step towards the final product.
Abigail Koss, Bin Yuan, Carsten Warneke, Jessica B. Gilman, Brian M. Lerner, Patrick R. Veres, Jeff Peischl, Scott Eilerman, Rob Wild, Steven S. Brown, Chelsea R. Thompson, Thomas Ryerson, Thomas Hanisco, Glenn M. Wolfe, Jason M. St. Clair, Mitchell Thayer, Frank N. Keutsch, Shane Murphy, and Joost de Gouw
Atmos. Meas. Tech., 10, 2941–2968, https://doi.org/10.5194/amt-10-2941-2017, https://doi.org/10.5194/amt-10-2941-2017, 2017
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Oil and gas extraction activity can cause air quality issues through emission of reactive chemicals. VOCs related to extraction operations in the United States were measured by PTR-ToF-MS from aircraft during the SONGNEX campaign in March–April 2015. The detailed analysis in this work provides a guide to interpreting PTR-ToF measurements in oil- and gas-producing regions, and it includes fundamental observations of VOC speciation and mixing ratios.
Shantanu H. Jathar, Christopher Heppding, Michael F. Link, Delphine K. Farmer, Ali Akherati, Michael J. Kleeman, Joost A. de Gouw, Patrick R. Veres, and James M. Roberts
Atmos. Chem. Phys., 17, 8959–8970, https://doi.org/10.5194/acp-17-8959-2017, https://doi.org/10.5194/acp-17-8959-2017, 2017
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Our work makes novel emissions measurements of isocyanic acid, a toxic gas, from a modern-day diesel engine and finds that diesel engines emit isocyanic acid but the emissions control devices do not enhance or destroy the isocyanic acid. Air quality model calculations suggest that diesel engines are possibly important sources of isocyanic acid in urban environments although the isocyanic acid levels are ten times lower than levels linked to adverse human health effects.
V. M. Erik Schenkeveld, Glen Jaross, Sergey Marchenko, David Haffner, Quintus L. Kleipool, Nico C. Rozemeijer, J. Pepijn Veefkind, and Pieternel F. Levelt
Atmos. Meas. Tech., 10, 1957–1986, https://doi.org/10.5194/amt-10-1957-2017, https://doi.org/10.5194/amt-10-1957-2017, 2017
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The Ozone Monitoring Instrument (OMI) has been flying on NASA’s EOS Aura satellite since July 15, 2004. It has measured the concentration of trace gasses in the atmosphere, like ozone, NO2 and SO2. This article describes the trend in performance and calibration parameters of OMI during 12 years of flight. The degradation of the CCD detectors, solar diffusers, spectral calibration and row anomaly are shown. The instrument shows overall degradation that is better than expected.
Bin Yuan, Matthew M. Coggon, Abigail R. Koss, Carsten Warneke, Scott Eilerman, Jeff Peischl, Kenneth C. Aikin, Thomas B. Ryerson, and Joost A. de Gouw
Atmos. Chem. Phys., 17, 4945–4956, https://doi.org/10.5194/acp-17-4945-2017, https://doi.org/10.5194/acp-17-4945-2017, 2017
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In this study, we measured emissions of volatile organic compounds (VOCs) from concentrated animal feeding operations (CAFOs) using both mobile laboratory and aircraft measurements. We will use this data set to investigate chemical compositions of VOC emissions and sources apportionment for these VOC emissions in different facilities.
Julien Chimot, J. Pepijn Veefkind, Tim Vlemmix, Johan F. de Haan, Vassilis Amiridis, Emmanouil Proestakis, Eleni Marinou, and Pieternel F. Levelt
Atmos. Meas. Tech., 10, 783–809, https://doi.org/10.5194/amt-10-783-2017, https://doi.org/10.5194/amt-10-783-2017, 2017
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We have developed artificial neural network algorithms to retrieve aerosol layer height from satellite OMI observations of the 477 nm O2–O2 spectral band. Based on 3-year (2005–2007) cloud-free scenes over north-east Asia, the results show uncertainties of 260–800 m when aerosol optical thickness is larger than 1. These algorithms also enable aerosol optical thickness retrievals by exploring the OMI continuum reflectance. These results may be used for future trace gas retrievals from TROPOMI.
Anusha P. S. Hettiyadura, Thilina Jayarathne, Karsten Baumann, Allen H. Goldstein, Joost A. de Gouw, Abigail Koss, Frank N. Keutsch, Kate Skog, and Elizabeth A. Stone
Atmos. Chem. Phys., 17, 1343–1359, https://doi.org/10.5194/acp-17-1343-2017, https://doi.org/10.5194/acp-17-1343-2017, 2017
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Organosulfates are components of secondary organic aerosol (SOA) formed in the presence of sulfate. Herein, their abundance, identity, and potential to form as sampling artifacts were studied in Centreville, AL, USA. The 10 most abundant signals accounted for 58–78 % of the total, with at least 20–200 other species accounting for the remainder. These major species were largely associated with biogenic gases, like isoprene and monoterpenes, and are proposed targets for future standard development.
Brian M. Lerner, Jessica B. Gilman, Kenneth C. Aikin, Elliot L. Atlas, Paul D. Goldan, Martin Graus, Roger Hendershot, Gabriel A. Isaacman-VanWertz, Abigail Koss, William C. Kuster, Richard A. Lueb, Richard J. McLaughlin, Jeff Peischl, Donna Sueper, Thomas B. Ryerson, Travis W. Tokarek, Carsten Warneke, Bin Yuan, and Joost A. de Gouw
Atmos. Meas. Tech., 10, 291–313, https://doi.org/10.5194/amt-10-291-2017, https://doi.org/10.5194/amt-10-291-2017, 2017
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Whole air sampling followed by analysis by gas chromatography is a common technique for characterization of trace volatile organic compounds in the atmosphere. We describe a new automated gas chromatograph–mass spectrograph which uses a Stirling cooler for sample preconcentration at −165 °C without the need for a cryogen such as liquid nitrogen. We also discuss potential sources of artifacts from our electropolished stainless steel sampling system and present results from two field campaigns.
Rachid Abida, Jean-Luc Attié, Laaziz El Amraoui, Philippe Ricaud, William Lahoz, Henk Eskes, Arjo Segers, Lyana Curier, Johan de Haan, Jukka Kujanpää, Albert Oude Nijhuis, Johanna Tamminen, Renske Timmermans, and Pepijn Veefkind
Atmos. Chem. Phys., 17, 1081–1103, https://doi.org/10.5194/acp-17-1081-2017, https://doi.org/10.5194/acp-17-1081-2017, 2017
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A detailed Observing System Simulation Experiment is performed to quantify the impact of future satellite instrument S-5P carbon monoxide (CO) on tropospheric analyses and forecasts. We focus on Europe for the period of northern summer 2003, when there was a severe heat wave episode. S-5P is able to capture the CO from forest fires that occurred in Portugal. Furthermore, our results provide evidence of S-5P CO benefits for monitoring processes contributing to atmospheric pollution.
J. Pepijn Veefkind, Johan F. de Haan, Maarten Sneep, and Pieternel F. Levelt
Atmos. Meas. Tech., 9, 6035–6049, https://doi.org/10.5194/amt-9-6035-2016, https://doi.org/10.5194/amt-9-6035-2016, 2016
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The Ozone Monitoring Instrument (OMI) on board the NASA EOS Aura satellite monitors the concentrations of trace gases. The accuracy of such observations relies partly on information on clouds. The OMI OMCLDO2 product derives the cloud fraction and pressure from the observed radiance in the visible. This paper reports on an improved version of this product. Compared to the previous version, the changes in cloud fraction are very small, but the changes in the cloud pressure can be significant.
Barbara Dix, Theodore K. Koenig, and Rainer Volkamer
Atmos. Meas. Tech., 9, 5655–5675, https://doi.org/10.5194/amt-9-5655-2016, https://doi.org/10.5194/amt-9-5655-2016, 2016
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We present a parameterization method for the conversion of measured trace gas slant column densities into volume mixing ratios along a flight track. Benefits of this method are that it is computationally fast and almost no information on local atmospheric conditions is needed. Application to simulated data and field data show that the method is accurate within 10–15 % and valid for a wide range of atmospheric conditions. Our method can easily be transferred to other trace gases.
Tomás Sherwen, Johan A. Schmidt, Mat J. Evans, Lucy J. Carpenter, Katja Großmann, Sebastian D. Eastham, Daniel J. Jacob, Barbara Dix, Theodore K. Koenig, Roman Sinreich, Ivan Ortega, Rainer Volkamer, Alfonso Saiz-Lopez, Cristina Prados-Roman, Anoop S. Mahajan, and Carlos Ordóñez
Atmos. Chem. Phys., 16, 12239–12271, https://doi.org/10.5194/acp-16-12239-2016, https://doi.org/10.5194/acp-16-12239-2016, 2016
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We present a simulation of tropospheric Cl, Br, I chemistry within the GEOS-Chem CTM. We find a decrease in tropospheric ozone burden of 18.6 % and a 8.2 % decrease in global mean OH concentrations. Cl oxidation of some VOCs range from 15 to 27 % of the total loss. Bromine plays a small role in oxidising oVOCs. Surface ozone, ozone sondes, and methane lifetime are in general improved by the inclusion of halogens. We argue that simulated bromine and chlorine represent a lower limit.
Weiwei Hu, Brett B. Palm, Douglas A. Day, Pedro Campuzano-Jost, Jordan E. Krechmer, Zhe Peng, Suzane S. de Sá, Scot T. Martin, M. Lizabeth Alexander, Karsten Baumann, Lina Hacker, Astrid Kiendler-Scharr, Abigail R. Koss, Joost A. de Gouw, Allen H. Goldstein, Roger Seco, Steven J. Sjostedt, Jeong-Hoo Park, Alex B. Guenther, Saewung Kim, Francesco Canonaco, André S. H. Prévôt, William H. Brune, and Jose L. Jimenez
Atmos. Chem. Phys., 16, 11563–11580, https://doi.org/10.5194/acp-16-11563-2016, https://doi.org/10.5194/acp-16-11563-2016, 2016
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IEPOX-SOA is biogenically derived secondary organic aerosol under anthropogenic influence, which has been shown to comprise a substantial fraction of OA globally. We investigated the lifetime of ambient IEPOX-SOA in the SE US and Amazonia, with an oxidation flow reactor and thermodenuder coupled with MS-based instrumentation. The low volatility and long lifetime of IEPOX-SOA against OH radicals' oxidation (> 2 weeks) was observed, which can help to constrain OA impact on air quality and climate.
J. Kaiser, K. M. Skog, K. Baumann, S. B. Bertman, S. B. Brown, W. H. Brune, J. D. Crounse, J. A. de Gouw, E. S. Edgerton, P. A. Feiner, A. H. Goldstein, A. Koss, P. K. Misztal, T. B. Nguyen, K. F. Olson, J. M. St. Clair, A. P. Teng, S. Toma, P. O. Wennberg, R. J. Wild, L. Zhang, and F. N. Keutsch
Atmos. Chem. Phys., 16, 9349–9359, https://doi.org/10.5194/acp-16-9349-2016, https://doi.org/10.5194/acp-16-9349-2016, 2016
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OH reactivity can be used to assess the amount of reactive carbon in an air mass. “Missing” reactivity is commonly found in forested environments and is attributed to either direct emissions of unmeasured volatile organic compounds or to unmeasured/underpredicted oxidation products. Using a box model and measurements from the 2013 SOAS campaign, we find only small discrepancies in measured and calculated reactivity. Our results suggest the discrepancies stem from unmeasured direct emissions.
Carsten Warneke, Michael Trainer, Joost A. de Gouw, David D. Parrish, David W. Fahey, A. R. Ravishankara, Ann M. Middlebrook, Charles A. Brock, James M. Roberts, Steven S. Brown, Jonathan A. Neuman, Brian M. Lerner, Daniel Lack, Daniel Law, Gerhard Hübler, Iliana Pollack, Steven Sjostedt, Thomas B. Ryerson, Jessica B. Gilman, Jin Liao, John Holloway, Jeff Peischl, John B. Nowak, Kenneth C. Aikin, Kyung-Eun Min, Rebecca A. Washenfelder, Martin G. Graus, Mathew Richardson, Milos Z. Markovic, Nick L. Wagner, André Welti, Patrick R. Veres, Peter Edwards, Joshua P. Schwarz, Timothy Gordon, William P. Dube, Stuart A. McKeen, Jerome Brioude, Ravan Ahmadov, Aikaterini Bougiatioti, Jack J. Lin, Athanasios Nenes, Glenn M. Wolfe, Thomas F. Hanisco, Ben H. Lee, Felipe D. Lopez-Hilfiker, Joel A. Thornton, Frank N. Keutsch, Jennifer Kaiser, Jingqiu Mao, and Courtney D. Hatch
Atmos. Meas. Tech., 9, 3063–3093, https://doi.org/10.5194/amt-9-3063-2016, https://doi.org/10.5194/amt-9-3063-2016, 2016
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In this paper we describe the experimental approach, the science goals and early results of the NOAA SENEX campaign, which was focused on studying the interactions between biogenic and anthropogenic emissions to form secondary pollutants.
During SENEX, the NOAA WP-3D aircraft conducted 20 research flights between 27 May and 10 July 2013 based out of Smyrna, TN. The SENEX flights included day- and nighttime flights in the Southeast as well as flights over areas with intense shale gas extraction.
Abigail R. Koss, Carsten Warneke, Bin Yuan, Matthew M. Coggon, Patrick R. Veres, and Joost A. de Gouw
Atmos. Meas. Tech., 9, 2909–2925, https://doi.org/10.5194/amt-9-2909-2016, https://doi.org/10.5194/amt-9-2909-2016, 2016
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Using laboratory and field experiments, we have explored how the technique of NO+ chemical ionization mass spectrometry can be used to measure volatile organic compounds (VOCs) in the troposphere. Results include the design and operation of the instrument, an evaluation of the technique’s utility for atmospheric measurement, and a guide for data interpretation. Use of this technique will improve our understanding of VOC chemistry.
Bin Yuan, Abigail Koss, Carsten Warneke, Jessica B. Gilman, Brian M. Lerner, Harald Stark, and Joost A. de Gouw
Atmos. Meas. Tech., 9, 2735–2752, https://doi.org/10.5194/amt-9-2735-2016, https://doi.org/10.5194/amt-9-2735-2016, 2016
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We present the development of a hydronium (H3O+) time of flight chemical ionization mass spectrometer (H3O+ ToF-CIMS). We characterize the humidity dependence of the reagent ions and VOC signals in details. The low mass cutoff issue of RF-only quadrupole leads to unusual humidity dependence of reagent ions. The new H3O+ ToF-CIMS was successfully deployed on the NOAA WP-3D research aircraft for the SONGNEX campaign in 2015 and some initial results from the SONGNEX campaign are presented.
Paul S. Romer, Kaitlin C. Duffey, Paul J. Wooldridge, Hannah M. Allen, Benjamin R. Ayres, Steven S. Brown, William H. Brune, John D. Crounse, Joost de Gouw, Danielle C. Draper, Philip A. Feiner, Juliane L. Fry, Allen H. Goldstein, Abigail Koss, Pawel K. Misztal, Tran B. Nguyen, Kevin Olson, Alex P. Teng, Paul O. Wennberg, Robert J. Wild, Li Zhang, and Ronald C. Cohen
Atmos. Chem. Phys., 16, 7623–7637, https://doi.org/10.5194/acp-16-7623-2016, https://doi.org/10.5194/acp-16-7623-2016, 2016
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The lifetime of nitrogen oxides (NOx) is evaluated by analysis of field measurements from the southeastern United States. At warm temperatures in the daytime boundary layer, NOx interconverts rapidly with both PAN and alkyl and multifunctional nitrates (RONO2), and the relevant lifetime is the combined lifetime of these three classes. We find that the production of RONO2, followed by hydrolysis to produce nitric acid, is the dominant pathway for NOx removal in an isoprene dominated forest.
Amber M. Ortega, Patrick L. Hayes, Zhe Peng, Brett B. Palm, Weiwei Hu, Douglas A. Day, Rui Li, Michael J. Cubison, William H. Brune, Martin Graus, Carsten Warneke, Jessica B. Gilman, William C. Kuster, Joost de Gouw, Cándido Gutiérrez-Montes, and Jose L. Jimenez
Atmos. Chem. Phys., 16, 7411–7433, https://doi.org/10.5194/acp-16-7411-2016, https://doi.org/10.5194/acp-16-7411-2016, 2016
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An oxidation flow reactor (OFR) was deployed to study secondary organic aerosol (SOA) formation and aging of urban emissions at a wide range of OH exposures during the CalNex campaign in Pasadena, CA, in 2010. Results include linking SOA formation to short-lived reactive compounds, similar elemental composition of reactor-aged emissions to atmospheric aging, changes in OA mass due to condensation of oxidized gas-phase species and heterogeneous oxidation of particle-phase species.
Sean Coburn, Barbara Dix, Eric Edgerton, Christopher D. Holmes, Douglas Kinnison, Qing Liang, Arnout ter Schure, Siyuan Wang, and Rainer Volkamer
Atmos. Chem. Phys., 16, 3743–3760, https://doi.org/10.5194/acp-16-3743-2016, https://doi.org/10.5194/acp-16-3743-2016, 2016
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Here we present a day of case study measurements of the vertical distribution of bromine monoxide over the coastal region of the Gulf of Mexico. These measurements are used to assess the contribution of bromine radicals to the oxidation of elemental mercury in the troposphere. We find that the measured levels of bromine in the troposphere are sufficient to quickly oxidize mercury, which has significant implications for our understanding of atmospheric mercury processes.
G. M. Wolfe, J. Kaiser, T. F. Hanisco, F. N. Keutsch, J. A. de Gouw, J. B. Gilman, M. Graus, C. D. Hatch, J. Holloway, L. W. Horowitz, B. H. Lee, B. M. Lerner, F. Lopez-Hilifiker, J. Mao, M. R. Marvin, J. Peischl, I. B. Pollack, J. M. Roberts, T. B. Ryerson, J. A. Thornton, P. R. Veres, and C. Warneke
Atmos. Chem. Phys., 16, 2597–2610, https://doi.org/10.5194/acp-16-2597-2016, https://doi.org/10.5194/acp-16-2597-2016, 2016
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This study uses airborne trace gas observations acquired over the southeast US to examine how both natural (isoprene) and anthropogenic (NOx) emissions influence the production of formaldehyde (HCHO). We find a 3-fold increase in HCHO yield between rural and polluted environments. State-of-the-science chemical mechanisms are generally able to reproduce this behavior. These results add confidence to global hydrocarbon emission inventories constrained by spaceborne HCHO observations.
Bin Yuan, John Liggio, Jeremy Wentzell, Shao-Meng Li, Harald Stark, James M. Roberts, Jessica Gilman, Brian Lerner, Carsten Warneke, Rui Li, Amy Leithead, Hans D. Osthoff, Robert Wild, Steven S. Brown, and Joost A. de Gouw
Atmos. Chem. Phys., 16, 2139–2153, https://doi.org/10.5194/acp-16-2139-2016, https://doi.org/10.5194/acp-16-2139-2016, 2016
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We describe high-resolution measurements of nitrated phenols using a time-of-flight chemical ionization mass spectrometer (ToF-CIMS). Strong diurnal profiles were observed for nitrated phenols, with concentration maxima at night. Box model simulations were able to reproduce the measured nitrated phenols.
T. Sherwen, M. J. Evans, L. J. Carpenter, S. J. Andrews, R. T. Lidster, B. Dix, T. K. Koenig, R. Sinreich, I. Ortega, R. Volkamer, A. Saiz-Lopez, C. Prados-Roman, A. S. Mahajan, and C. Ordóñez
Atmos. Chem. Phys., 16, 1161–1186, https://doi.org/10.5194/acp-16-1161-2016, https://doi.org/10.5194/acp-16-1161-2016, 2016
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Using a global chemical transport model (GEOS-Chem) with additional iodine emissions, chemistry, and deposition we show that iodine is responsible for ~ 9 % of global ozone loss but has negligible impacts on global OH. Uncertainties are large in the chemistry and emissions and future research is needed in both. Measurements of iodine species (especially HOI) would be useful. We believe iodine chemistry should be considered in future chemistry-climate and in air quality modelling.
R. J. Wild, P. M. Edwards, T. S. Bates, R. C. Cohen, J. A. de Gouw, W. P. Dubé, J. B. Gilman, J. Holloway, J. Kercher, A. R. Koss, L. Lee, B. M. Lerner, R. McLaren, P. K. Quinn, J. M. Roberts, J. Stutz, J. A. Thornton, P. R. Veres, C. Warneke, E. Williams, C. J. Young, B. Yuan, K. J. Zarzana, and S. S. Brown
Atmos. Chem. Phys., 16, 573–583, https://doi.org/10.5194/acp-16-573-2016, https://doi.org/10.5194/acp-16-573-2016, 2016
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High wintertime ozone levels have been observed in the Uintah Basin, Utah, a sparsely populated rural region with intensive oil and gas operations. The reactive nitrogen budget plays an important role in tropospheric ozone formation, and we find that nighttime chemistry has a large effect on its partitioning. Much of the oxidation of reactive nitrogen during a high-ozone year occurred via heterogeneous uptake onto aerosol at night, keeping NOx at concentrations comparable to a low-ozone year.
J. B. Gilman, B. M. Lerner, W. C. Kuster, P. D. Goldan, C. Warneke, P. R. Veres, J. M. Roberts, J. A. de Gouw, I. R. Burling, and R. J. Yokelson
Atmos. Chem. Phys., 15, 13915–13938, https://doi.org/10.5194/acp-15-13915-2015, https://doi.org/10.5194/acp-15-13915-2015, 2015
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A comprehensive suite of instruments was used to quantify the emissions of over 200 organic and inorganic gases from 56 laboratory burns of 18 different biomass fuel types common in the southeastern, southwestern, or northern United States. Emission ratios relative to carbon monoxide (CO) are used to characterize the composition of gases emitted by mass; OH reactivity; and potential secondary organic aerosol (SOA) precursors for the three different U.S. fuel regions presented here.
B. R. Ayres, H. M. Allen, D. C. Draper, S. S. Brown, R. J. Wild, J. L. Jimenez, D. A. Day, P. Campuzano-Jost, W. Hu, J. de Gouw, A. Koss, R. C. Cohen, K. C. Duffey, P. Romer, K. Baumann, E. Edgerton, S. Takahama, J. A. Thornton, B. H. Lee, F. D. Lopez-Hilfiker, C. Mohr, P. O. Wennberg, T. B. Nguyen, A. Teng, A. H. Goldstein, K. Olson, and J. L. Fry
Atmos. Chem. Phys., 15, 13377–13392, https://doi.org/10.5194/acp-15-13377-2015, https://doi.org/10.5194/acp-15-13377-2015, 2015
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This paper reports atmospheric gas- and aerosol-phase field measurements from the southeastern United States in summer 2013 to demonstrate that the oxidation of biogenic volatile organic compounds by nitrate radical produces a substantial amount of secondary organic aerosol in this region. This process, driven largely by monoterpenes, results in a comparable aerosol nitrate production rate to inorganic nitrate formation by heterogeneous uptake of HNO3 onto dust particles.
F. Xiong, K. M. McAvey, K. A. Pratt, C. J. Groff, M. A. Hostetler, M. A. Lipton, T. K. Starn, J. V. Seeley, S. B. Bertman, A. P. Teng, J. D. Crounse, T. B. Nguyen, P. O. Wennberg, P. K. Misztal, A. H. Goldstein, A. B. Guenther, A. R. Koss, K. F. Olson, J. A. de Gouw, K. Baumann, E. S. Edgerton, P. A. Feiner, L. Zhang, D. O. Miller, W. H. Brune, and P. B. Shepson
Atmos. Chem. Phys., 15, 11257–11272, https://doi.org/10.5194/acp-15-11257-2015, https://doi.org/10.5194/acp-15-11257-2015, 2015
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Hydroxynitrates from isoprene oxidation were quantified both in the laboratory and through field studies. The yield of hydroxynitrates 9(+4/-3)% derived from chamber experiments was applied in a zero-dimensional model to simulate the production and loss of isoprene hydroxynitrates in an ambient environment during the 2013 Southern Oxidant and Aerosol Study (SOAS). NOx was determined to be the limiting factor for the formation of isoprene hydroxynitrates during SOAS.
C. Huang, H. L. Wang, L. Li, Q. Wang, Q. Lu, J. A. de Gouw, M. Zhou, S. A. Jing, J. Lu, and C. H. Chen
Atmos. Chem. Phys., 15, 11081–11096, https://doi.org/10.5194/acp-15-11081-2015, https://doi.org/10.5194/acp-15-11081-2015, 2015
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SOA formations from vehicle exhausts and gas evaporation contribute 40% and 60% of total organic aerosols observed in summer and winter in urban Shanghai. Diesel vehicles, which accounted for less than 20% of vehicle kilometers of travel, contribute the most to vehicular POA emissions and SOA production in urban Shanghai. Intermediate-volatile organic compounds (IVOCs) in vehicle exhausts contribute greatly to SOA formation in the urban atmosphere of China.
L. Lee, P. J. Wooldridge, J. deGouw, S. S. Brown, T. S. Bates, P. K. Quinn, and R. C. Cohen
Atmos. Chem. Phys., 15, 9313–9325, https://doi.org/10.5194/acp-15-9313-2015, https://doi.org/10.5194/acp-15-9313-2015, 2015
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Secondary organic aerosol affects both the environment and human health. We characterized the aerosol composition in Uintah Basin by measuring the concentration of nitrooxy group moiety which is produced through chemical interaction of volatile organic compounds and NOx emitted largely from local human activity. We found nitrooxy compounds to be a persistent, if not dominant, portion of fine aerosol mass. Similar results may be expected from emissions due to traffic in cities.
P. R. Veres, J. M. Roberts, R. J. Wild, P. M. Edwards, S. S. Brown, T. S. Bates, P. K. Quinn, J. E. Johnson, R. J. Zamora, and J. de Gouw
Atmos. Chem. Phys., 15, 8101–8114, https://doi.org/10.5194/acp-15-8101-2015, https://doi.org/10.5194/acp-15-8101-2015, 2015
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In this paper laboratory work is documented establishing iodide ion chemical ionization mass spectrometry (I- CIMS) as a sensitive method for the unambiguous detection of peroxynitric acid (HO2NO2; PNA). A dynamic calibration source for HO2NO2, HO2, and HONO was developed and calibrated using a novel total NOy detector (NOy CaRDS). The ambient observations of HO2NO2 using I- CIMS made during the 2013 and 2014 Uintah Basin Wintertime Ozone Study (UBWOS) are presented.
J. Kaiser, G. M. Wolfe, K. E. Min, S. S. Brown, C. C. Miller, D. J. Jacob, J. A. deGouw, M. Graus, T. F. Hanisco, J. Holloway, J. Peischl, I. B. Pollack, T. B. Ryerson, C. Warneke, R. A. Washenfelder, and F. N. Keutsch
Atmos. Chem. Phys., 15, 7571–7583, https://doi.org/10.5194/acp-15-7571-2015, https://doi.org/10.5194/acp-15-7571-2015, 2015
N. L. Wagner, C. A. Brock, W. M. Angevine, A. Beyersdorf, P. Campuzano-Jost, D. Day, J. A. de Gouw, G. S. Diskin, T. D. Gordon, M. G. Graus, J. S. Holloway, G. Huey, J. L. Jimenez, D. A. Lack, J. Liao, X. Liu, M. Z. Markovic, A. M. Middlebrook, T. Mikoviny, J. Peischl, A. E. Perring, M. S. Richardson, T. B. Ryerson, J. P. Schwarz, C. Warneke, A. Welti, A. Wisthaler, L. D. Ziemba, and D. M. Murphy
Atmos. Chem. Phys., 15, 7085–7102, https://doi.org/10.5194/acp-15-7085-2015, https://doi.org/10.5194/acp-15-7085-2015, 2015
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This paper investigates the summertime vertical profile of aerosol over the southeastern US using in situ measurements collected from aircraft. We use a vertical mixing model and measurements of CO to predict the vertical profile of aerosol that we would expect from vertical mixing alone and compare with the observed aerosol profile. We found a modest enhancement of aerosol in the cloudy transition layer during shallow cumulus convection and attribute the enhancement to local aerosol formation.
D. B. Millet, M. Baasandorj, D. K. Farmer, J. A. Thornton, K. Baumann, P. Brophy, S. Chaliyakunnel, J. A. de Gouw, M. Graus, L. Hu, A. Koss, B. H. Lee, F. D. Lopez-Hilfiker, J. A. Neuman, F. Paulot, J. Peischl, I. B. Pollack, T. B. Ryerson, C. Warneke, B. J. Williams, and J. Xu
Atmos. Chem. Phys., 15, 6283–6304, https://doi.org/10.5194/acp-15-6283-2015, https://doi.org/10.5194/acp-15-6283-2015, 2015
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Formic acid (HCOOH) is an abundant atmospheric acid that affects precipitation chemistry and acidity. HCOOH measurements over the USA are 2-3× larger than can be explained by known sources and sinks, revealing a key gap in current understanding. Observations indicate a large biogenic source plus chemical production across a range of precursors. Model simulations cannot capture the HCOOH diurnal amplitude or nocturnal profile, implying a deposition bias and possibly even larger missing source.
P. L. Hayes, A. G. Carlton, K. R. Baker, R. Ahmadov, R. A. Washenfelder, S. Alvarez, B. Rappenglück, J. B. Gilman, W. C. Kuster, J. A. de Gouw, P. Zotter, A. S. H. Prévôt, S. Szidat, T. E. Kleindienst, J. H. Offenberg, P. K. Ma, and J. L. Jimenez
Atmos. Chem. Phys., 15, 5773–5801, https://doi.org/10.5194/acp-15-5773-2015, https://doi.org/10.5194/acp-15-5773-2015, 2015
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(1) Four different parameterizations for the formation and chemical evolution of secondary organic aerosol (SOA) are evaluated using a box model representing the Los Angeles region during the CalNex campaign.
(2) The SOA formed only from the oxidation of VOCs is insufficient to explain the observed SOA concentrations.
(3) The amount of SOA mass formed from diesel vehicle emissions is estimated to be 16-27%.
(4) Modeled SOA depends strongly on the P-S/IVOC volatility distribution.
A. R. Koss, J. de Gouw, C. Warneke, J. B. Gilman, B. M. Lerner, M. Graus, B. Yuan, P. Edwards, S. S. Brown, R. Wild, J. M. Roberts, T. S. Bates, and P. K. Quinn
Atmos. Chem. Phys., 15, 5727–5741, https://doi.org/10.5194/acp-15-5727-2015, https://doi.org/10.5194/acp-15-5727-2015, 2015
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Extraction of natural gas and oil is associated with a range of possible atmospheric environmental issues. Here we present an analysis of gas-phase hydrocarbon measurements taken in an oil and natural gas extraction area in Utah during a period of high wintertime ozone. We are able to constrain important chemical parameters related to emission sources and rates, hydrocarbon photochemistry, and VOC composition.
R. Volkamer, S. Baidar, T. L. Campos, S. Coburn, J. P. DiGangi, B. Dix, E. W. Eloranta, T. K. Koenig, B. Morley, I. Ortega, B. R. Pierce, M. Reeves, R. Sinreich, S. Wang, M. A. Zondlo, and P. A. Romashkin
Atmos. Meas. Tech., 8, 2121–2148, https://doi.org/10.5194/amt-8-2121-2015, https://doi.org/10.5194/amt-8-2121-2015, 2015
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Tropospheric halogens and small oxygenated VOC (OVOC) modify tropospheric HOx and NOx, O3 and aerosols. We have measured bromine monoxide (BrO), iodine monoxide (IO), glyoxal (CHOCHO) profiles from research aircraft in the tropical troposphere and compare with ship- and aircraft-based in situ sensors. Our measurements point to the need to improve the representation of halogens and organic carbon sources in atmospheric models.
K. R. Baker, A. G. Carlton, T. E. Kleindienst, J. H. Offenberg, M. R. Beaver, D. R. Gentner, A. H. Goldstein, P. L. Hayes, J. L. Jimenez, J. B. Gilman, J. A. de Gouw, M. C. Woody, H. O. T. Pye, J. T. Kelly, M. Lewandowski, M. Jaoui, P. S. Stevens, W. H. Brune, Y.-H. Lin, C. L. Rubitschun, and J. D. Surratt
Atmos. Chem. Phys., 15, 5243–5258, https://doi.org/10.5194/acp-15-5243-2015, https://doi.org/10.5194/acp-15-5243-2015, 2015
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This work details the evaluation of PM2.5 carbon, VOC precursors, and OH estimated by the CMAQ photochemical transport model using routine and special measurements from the 2010 CalNex field study. Here, CMAQ and most recent emissions inventory (2011 NEI) are used to generate model PM2.5 OC estimates that are examined in novel ways including primary vs. secondary formation, fossil vs. contemporary carbon, OH and HO2 evaluation, and the relationship between key VOC precursors and SOC tracers.
J. H. G. M. van Geffen, K. F. Boersma, M. Van Roozendael, F. Hendrick, E. Mahieu, I. De Smedt, M. Sneep, and J. P. Veefkind
Atmos. Meas. Tech., 8, 1685–1699, https://doi.org/10.5194/amt-8-1685-2015, https://doi.org/10.5194/amt-8-1685-2015, 2015
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The paper describes improvements to the algorithm for the retrieval of nitrogen dioxide (NO2) concentration from measurements of the Ozone Monitoring Instrument (OMI), launched on board NASA's EOS-Aura satellite in 2004. With these improvements - updates of the wavelength calibration and the reference spectra - the OMI results are consistent with independent NO2 measurements and the overall quality of the spectral fit is improved considerably.
B. Yuan, P. R. Veres, C. Warneke, J. M. Roberts, J. B. Gilman, A. Koss, P. M. Edwards, M. Graus, W. C. Kuster, S.-M. Li, R. J. Wild, S. S. Brown, W. P. Dubé, B. M. Lerner, E. J. Williams, J. E. Johnson, P. K. Quinn, T. S. Bates, B. Lefer, P. L. Hayes, J. L. Jimenez, R. J. Weber, R. Zamora, B. Ervens, D. B. Millet, B. Rappenglück, and J. A. de Gouw
Atmos. Chem. Phys., 15, 1975–1993, https://doi.org/10.5194/acp-15-1975-2015, https://doi.org/10.5194/acp-15-1975-2015, 2015
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In this work, secondary formation of formic acid at an urban site and a site in an oil and gas production region is studied. We investigated various gas phase formation pathways of formic acid, including those recently proposed, using a box model. The contributions from aerosol-related processes, fog events and air-snow exchange to formic acid are also quantified.
E. Spinei, A. Cede, J. Herman, G. H. Mount, E. Eloranta, B. Morley, S. Baidar, B. Dix, I. Ortega, T. Koenig, and R. Volkamer
Atmos. Meas. Tech., 8, 793–809, https://doi.org/10.5194/amt-8-793-2015, https://doi.org/10.5194/amt-8-793-2015, 2015
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This paper presents ground-based direct-sun and airborne multi-axis DOAS measurements of O2O2 absorption optical depths under atmospheric conditions in two wavelength regions (335-–390nm and 435--490nm). Our results show that laboratory-measured σ(O2O2) is applicable for observations over a wide range of atmospheric conditions. Temperature dependence of σ(O2O2) is about 9±2.5% from 231K to 275K.
C. Warneke, P. Veres, S. M. Murphy, J. Soltis, R. A. Field, M. G. Graus, A. Koss, S.-M. Li, R. Li, B. Yuan, J. M. Roberts, and J. A. de Gouw
Atmos. Meas. Tech., 8, 411–420, https://doi.org/10.5194/amt-8-411-2015, https://doi.org/10.5194/amt-8-411-2015, 2015
R. Ahmadov, S. McKeen, M. Trainer, R. Banta, A. Brewer, S. Brown, P. M. Edwards, J. A. de Gouw, G. J. Frost, J. Gilman, D. Helmig, B. Johnson, A. Karion, A. Koss, A. Langford, B. Lerner, J. Olson, S. Oltmans, J. Peischl, G. Pétron, Y. Pichugina, J. M. Roberts, T. Ryerson, R. Schnell, C. Senff, C. Sweeney, C. Thompson, P. R. Veres, C. Warneke, R. Wild, E. J. Williams, B. Yuan, and R. Zamora
Atmos. Chem. Phys., 15, 411–429, https://doi.org/10.5194/acp-15-411-2015, https://doi.org/10.5194/acp-15-411-2015, 2015
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High 2013 wintertime O3 pollution events associated with oil/gas production within the Uinta Basin are studied using a 3D model. It's able quantitatively to reproduce these events using emission estimates of O3 precursors based on ambient measurements (top-down approach), but unable to reproduce them using a recent bottom-up emission inventory for the oil/gas industry. The role of various physical and meteorological processes, chemical species and pathways contributing to high O3 are quantified.
L. Lee, P. J. Wooldridge, J. B. Gilman, C. Warneke, J. de Gouw, and R. C. Cohen
Atmos. Chem. Phys., 14, 12441–12454, https://doi.org/10.5194/acp-14-12441-2014, https://doi.org/10.5194/acp-14-12441-2014, 2014
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Alkyl nitrate formation is known to be an important sink of NOx in a wide range of environments. In a study in the Uintah basin in 2012, we find that formation of these compounds represents a more rapid NOx (NO + NO2) sink than does nitric acid formation. This rapid formation is in large part due to the low mean temperature (~0°C) during the study and is consistent with laboratory observations.
Y. You, V. P. Kanawade, J. A. de Gouw, A. B. Guenther, S. Madronich, M. R. Sierra-Hernández, M. Lawler, J. N. Smith, S. Takahama, G. Ruggeri, A. Koss, K. Olson, K. Baumann, R. J. Weber, A. Nenes, H. Guo, E. S. Edgerton, L. Porcelli, W. H. Brune, A. H. Goldstein, and S.-H. Lee
Atmos. Chem. Phys., 14, 12181–12194, https://doi.org/10.5194/acp-14-12181-2014, https://doi.org/10.5194/acp-14-12181-2014, 2014
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Amiens play important roles in atmospheric secondary aerosol formation and human health, but the fast response measurements of amines are lacking. Here we show measurements in a southeastern US forest and a moderately polluted midwestern site. Our results show that gas to particle conversion is an important process that controls ambient amine concentrations and that biomass burning is an important source of amines.
R. Li, C. Warneke, M. Graus, R. Field, F. Geiger, P. R. Veres, J. Soltis, S.-M. Li, S. M. Murphy, C. Sweeney, G. Pétron, J. M. Roberts, and J. de Gouw
Atmos. Meas. Tech., 7, 3597–3610, https://doi.org/10.5194/amt-7-3597-2014, https://doi.org/10.5194/amt-7-3597-2014, 2014
C. Warneke, F. Geiger, P. M. Edwards, W. Dube, G. Pétron, J. Kofler, A. Zahn, S. S. Brown, M. Graus, J. B. Gilman, B. M. Lerner, J. Peischl, T. B. Ryerson, J. A. de Gouw, and J. M. Roberts
Atmos. Chem. Phys., 14, 10977–10988, https://doi.org/10.5194/acp-14-10977-2014, https://doi.org/10.5194/acp-14-10977-2014, 2014
W. Ait-Helal, A. Borbon, S. Sauvage, J. A. de Gouw, A. Colomb, V. Gros, F. Freutel, M. Crippa, C. Afif, U. Baltensperger, M. Beekmann, J.-F. Doussin, R. Durand-Jolibois, I. Fronval, N. Grand, T. Leonardis, M. Lopez, V. Michoud, K. Miet, S. Perrier, A. S. H. Prévôt, J. Schneider, G. Siour, P. Zapf, and N. Locoge
Atmos. Chem. Phys., 14, 10439–10464, https://doi.org/10.5194/acp-14-10439-2014, https://doi.org/10.5194/acp-14-10439-2014, 2014
M. Belmonte Rivas, P. Veefkind, F. Boersma, P. Levelt, H. Eskes, and J. Gille
Atmos. Meas. Tech., 7, 2203–2225, https://doi.org/10.5194/amt-7-2203-2014, https://doi.org/10.5194/amt-7-2203-2014, 2014
D. R. Gentner, T. B. Ford, A. Guha, K. Boulanger, J. Brioude, W. M. Angevine, J. A. de Gouw, C. Warneke, J. B. Gilman, T. B. Ryerson, J. Peischl, S. Meinardi, D. R. Blake, E. Atlas, W. A. Lonneman, T. E. Kleindienst, M. R. Beaver, J. M. St. Clair, P. O. Wennberg, T. C. VandenBoer, M. Z. Markovic, J. G. Murphy, R. A. Harley, and A. H. Goldstein
Atmos. Chem. Phys., 14, 4955–4978, https://doi.org/10.5194/acp-14-4955-2014, https://doi.org/10.5194/acp-14-4955-2014, 2014
A. Määttä, M. Laine, J. Tamminen, and J. P. Veefkind
Atmos. Meas. Tech., 7, 1185–1199, https://doi.org/10.5194/amt-7-1185-2014, https://doi.org/10.5194/amt-7-1185-2014, 2014
C. A. McLinden, V. Fioletov, K. F. Boersma, S. K. Kharol, N. Krotkov, L. Lamsal, P. A. Makar, R. V. Martin, J. P. Veefkind, and K. Yang
Atmos. Chem. Phys., 14, 3637–3656, https://doi.org/10.5194/acp-14-3637-2014, https://doi.org/10.5194/acp-14-3637-2014, 2014
K. C. Wells, D. B. Millet, K. E. Cady-Pereira, M. W. Shephard, D. K. Henze, N. Bousserez, E. C. Apel, J. de Gouw, C. Warneke, and H. B. Singh
Atmos. Chem. Phys., 14, 2555–2570, https://doi.org/10.5194/acp-14-2555-2014, https://doi.org/10.5194/acp-14-2555-2014, 2014
J. J. Ensberg, P. L. Hayes, J. L. Jimenez, J. B. Gilman, W. C. Kuster, J. A. de Gouw, J. S. Holloway, T. D. Gordon, S. Jathar, A. L. Robinson, and J. H. Seinfeld
Atmos. Chem. Phys., 14, 2383–2397, https://doi.org/10.5194/acp-14-2383-2014, https://doi.org/10.5194/acp-14-2383-2014, 2014
A. M. Ortega, D. A. Day, M. J. Cubison, W. H. Brune, D. Bon, J. A. de Gouw, and J. L. Jimenez
Atmos. Chem. Phys., 13, 11551–11571, https://doi.org/10.5194/acp-13-11551-2013, https://doi.org/10.5194/acp-13-11551-2013, 2013
S. S. Brown, W. P. Dubé, R. Bahreini, A. M. Middlebrook, C. A. Brock, C. Warneke, J. A. de Gouw, R. A. Washenfelder, E. Atlas, J. Peischl, T. B. Ryerson, J. S. Holloway, J. P. Schwarz, R. Spackman, M. Trainer, D. D. Parrish, F. C. Fehshenfeld, and A. R. Ravishankara
Atmos. Chem. Phys., 13, 11317–11337, https://doi.org/10.5194/acp-13-11317-2013, https://doi.org/10.5194/acp-13-11317-2013, 2013
P. M. Edwards, C. J. Young, K. Aikin, J. deGouw, W. P. Dubé, F. Geiger, J. Gilman, D. Helmig, J. S. Holloway, J. Kercher, B. Lerner, R. Martin, R. McLaren, D. D. Parrish, J. Peischl, J. M. Roberts, T. B. Ryerson, J. Thornton, C. Warneke, E. J. Williams, and S. S. Brown
Atmos. Chem. Phys., 13, 8955–8971, https://doi.org/10.5194/acp-13-8955-2013, https://doi.org/10.5194/acp-13-8955-2013, 2013
S. Baidar, H. Oetjen, S. Coburn, B. Dix, I. Ortega, R. Sinreich, and R. Volkamer
Atmos. Meas. Tech., 6, 719–739, https://doi.org/10.5194/amt-6-719-2013, https://doi.org/10.5194/amt-6-719-2013, 2013
R. J. Yokelson, I. R. Burling, J. B. Gilman, C. Warneke, C. E. Stockwell, J. de Gouw, S. K. Akagi, S. P. Urbanski, P. Veres, J. M. Roberts, W. C. Kuster, J. Reardon, D. W. T. Griffith, T. J. Johnson, S. Hosseini, J. W. Miller, D. R. Cocker III, H. Jung, and D. R. Weise
Atmos. Chem. Phys., 13, 89–116, https://doi.org/10.5194/acp-13-89-2013, https://doi.org/10.5194/acp-13-89-2013, 2013
Related subject area
Subject: Gases | Technique: Remote Sensing | Topic: Data Processing and Information Retrieval
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Remote sensing of lower-middle-thermosphere temperatures using the N2 Lyman–Birge–Hopfield (LBH) bands
Retrievals of water vapour and temperature exploiting the far-infrared: application to aircraft observations in preparation for the FORUM mission
Global decadal measurements of methanol, ethene, ethyne, and HCN from the Cross-track Infrared Sounder
Forward model emulator for atmospheric radiative transfer using Gaussian processes and cross validation
Developments on a 22 GHz microwave radiometer and reprocessing of 13-year time series for water vapour studies
Optimal selection of satellite XCO2 images for urban CO2 emission monitoring
Separating and quantifying facility-level methane emissions with overlapping plumes for spaceborne methane monitoring
A study of measurement scenarios for the future CO2M mission: avoidance of detector saturation and the impact on XCO2 retrievals
Retrieving the atmospheric concentrations of carbon dioxide and methane from the European Copernicus CO2M satellite mission using artificial neural networks
Surface reflectance biases in XCH4 retrievals from the 2.3 μm band are enhanced in the presence of aerosols
Remote sensing of methane point sources with the MethaneAIR airborne spectrometer
The differences between remote sensing and in situ air pollutant measurements over the Canadian oil sands
NitroNet – a machine learning model for the prediction of tropospheric NO2 profiles from TROPOMI observations
Improved convective cloud differential (CCD) tropospheric ozone from S5P-TROPOMI satellite data using local cloud fields
Atmospheric propane (C3H8) column retrievals from ground-based FTIR observations in Xianghe, China
Hourly surface nitrogen dioxide retrieval from GEMS tropospheric vertical column densities: Benefit of using time-contiguous input features for machine learning models
Can the remote sensing of combustion phase improve estimates of landscape fire smoke emission rate and composition?
Tropospheric NO2 retrieval algorithm for geostationary satellite instruments: applications to GEMS
Troposphere–stratosphere-integrated bromine monoxide (BrO) profile retrieval over the central Pacific Ocean
Local and regional enhancements of CH4, CO, and CO2 inferred from TCCON column measurements
Merging TEMPEST microwave and GOES-16 geostationary IR soundings for improved water vapor profiles
Remote Sensing Estimates of Time-Resolved HONO and NO2 Emission Rates and Lifetimes in Wildfires
Assimilation of volcanic sulfur dioxide products from IASI and TROPOMI into the chemical transport model MOCAGE: case study of the 2021 La Soufrière Saint-Vincent eruption
Methane retrieval from MethaneAIR using the CO2 proxy approach: a demonstration for the upcoming MethaneSAT mission
Mapping the CO2 total column retrieval performance from shortwave infrared measurements: synthetic impacts of the spectral resolution, signal-to-noise ratio, and spectral band selection
Assessment of the contribution of the Meteosat Third Generation Infrared Sounder (MTG-IRS) for the characterisation of ozone over Europe
Assessing the potential of free-tropospheric water vapour isotopologue satellite observations for improving the analyses of convective events
Current potential of CH4 emission estimates using TROPOMI in the Middle East
A bias-corrected GEMS geostationary satellite product for nitrogen dioxide using machine learning to enforce consistency with the TROPOMI satellite instrument
Estimation of biogenic volatile organic compound (BVOC) emissions in forest ecosystems using drone-based lidar, photogrammetry, and image recognition technologies
Fast retrieval of XCO2 over east Asia based on Orbiting Carbon Observatory-2 (OCO-2) spectral measurements
A new method for estimating megacity NOx emissions and lifetimes from satellite observations
Accounting for the effect of aerosols in GHGSat methane retrieval
A survey of methane point source emissions from coal mines in Shanxi province of China using AHSI on board Gaofen-5B
Global retrieval of stratospheric and tropospheric BrO columns from the Ozone Mapping and Profiler Suite Nadir Mapper (OMPS-NM) on board the Suomi-NPP satellite
IMK–IAA MIPAS retrieval version 8: CH4 and N2O
Report on Landsat 8 and Sentinel-2B observations of the Nord Stream 2 pipeline methane leak
U-Plume: automated algorithm for plume detection and source quantification by satellite point-source imagers
CH4Net: a deep learning model for monitoring methane super-emitters with Sentinel-2 imagery
Greenhouse gas retrievals for the CO2M mission using the FOCAL method: first performance estimates
Quantitative imaging of carbon dioxide plumes using a ground-based shortwave infrared spectral camera
The transition to new ozone absorption cross sections for Dobson and Brewer total ozone measurements
Jihanne El Haouari, Jean-Michel Gaucel, Christelle Pittet, Jean-Yves Tourneret, and Herwig Wendt
Atmos. Meas. Tech., 18, 2573–2590, https://doi.org/10.5194/amt-18-2573-2025, https://doi.org/10.5194/amt-18-2573-2025, 2025
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This paper explores new techniques based on sparse representations for estimating the spectral response functions of high-resolution spectrometers. The method is highly competitive, with commonly used parametric models yielding more accurate estimates while accounting for wavelength dependence. The resulting normalized estimation errors of the spectrometer spectral responses are less than 1 %, which will allow for better quantification of trace gas concentrations at the Earth surface.
Bavo Langerock, Martine De Mazière, Filip Desmet, Pauli Heikkinen, Rigel Kivi, Mahesh Kumar Sha, Corinne Vigouroux, Minqiang Zhou, Gopala Krishna Darbha, and Mohmmed Talib
Atmos. Meas. Tech., 18, 2439–2446, https://doi.org/10.5194/amt-18-2439-2025, https://doi.org/10.5194/amt-18-2439-2025, 2025
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Ground-based Fourier transform interferometer instruments have been used for many decades to measure direct solar light in the infrared to obtain high-resolution spectra from which atmospheric gas profile concentrations can be derived. It is shown that the typical processing chain used to derive atmospheric gas columns can be sensitive to relatively small shortenings of the recorded interferograms. Low-resolution recordings, used in more recent years, are more sensitive to such adaptations.
Ramina Alwarda, Kristof Bognar, Xiaoyi Zhao, Vitali Fioletov, Jonathan Davies, Sum Chi Lee, Debora Griffin, Alexandru Lupu, Udo Frieß, Alexander Cede, Yushan Su, and Kimberly Strong
Atmos. Meas. Tech., 18, 2397–2423, https://doi.org/10.5194/amt-18-2397-2025, https://doi.org/10.5194/amt-18-2397-2025, 2025
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Nitrogen dioxide (NO2) is a pollutant with a short lifetime and large variability, but there are limited measurements of its distribution in the lower atmosphere. We present a new 3-year dataset of NO2 vertical profiles in Toronto, Canada, and evaluate it using NO2 from satellite and surface monitoring networks and simulations by an air quality forecast model. We quantify and explain the differences among the datasets to provide information that can be used to understand NO2 variability.
Xinyu Li, Lin Zhu, Hongfu Sun, Jun Li, Ximing Lv, Chengli Qi, and Huanhuan Yan
Atmos. Meas. Tech., 18, 2333–2352, https://doi.org/10.5194/amt-18-2333-2025, https://doi.org/10.5194/amt-18-2333-2025, 2025
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This paper proposes a novel methodology for selecting sulfur-dioxide-sensitive channels from FY-3E/HIRAS-II hyperspectral IR atmospheric sensors to quantitatively monitor volcanic sulfur dioxide. This methodology considers the interference of atmospheric temperature, humidity, and surface temperature with sulfur dioxide detection and retrieval, laying the groundwork for developing a more accurate and flexible volcanic sulfur dioxide retrieval algorithm under different atmospheric conditions.
Edward Malina, Jure Brence, Jennifer Adams, Jovan Tanevski, Sašo Džeroski, Valentin Kantchev, and Kevin W. Bowman
Atmos. Meas. Tech., 18, 1689–1715, https://doi.org/10.5194/amt-18-1689-2025, https://doi.org/10.5194/amt-18-1689-2025, 2025
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The large fleet of Earth observation satellites in orbit currently generate huge volumes of data, requiring significant computational resources to process these data in a timely manner. We present a method for predicting poor-quality measurements using machine learning. We find that machine learning methods can accurately predict poor-quality measurements and remove them from the processing chain, saving time and computational resources.
Yuhang Zhang, Huan Yu, Isabelle De Smedt, Jintai Lin, Nicolas Theys, Michel Van Roozendael, Gaia Pinardi, Steven Compernolle, Ruijing Ni, Fangxuan Ren, Sijie Wang, Lulu Chen, Jos Van Geffen, Mengyao Liu, Alexander M. Cede, Martin Tiefengraber, Alexis Merlaud, Martina M. Friedrich, Andreas Richter, Ankie Piters, Vinod Kumar, Vinayak Sinha, Thomas Wagner, Yongjoo Choi, Hisahiro Takashima, Yugo Kanaya, Hitoshi Irie, Robert Spurr, Wenfu Sun, and Lorenzo Fabris
Atmos. Meas. Tech., 18, 1561–1589, https://doi.org/10.5194/amt-18-1561-2025, https://doi.org/10.5194/amt-18-1561-2025, 2025
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We developed an advanced algorithm for global retrieval of TROPOspheric Monitoring Instrument (TROPOMI) HCHO and NO2 vertical column densities with much improved consistency. Sensitivity tests demonstrate the complexity and nonlinear interactions of auxiliary parameters in the air mass factor calculation. An improved agreement is found with measurements from a global ground-based instrument network. The scientific retrieval provides a useful source of information for studies combining HCHO and NO2.
Tannaz H. Mohammadloo, Matthew Jones, Bas van de Kerkhof, Kyle Dawson, Brendan J. Smith, Stephen Conley, Abigail Corbett, and Rutger IJzermans
Atmos. Meas. Tech., 18, 1301–1324, https://doi.org/10.5194/amt-18-1301-2025, https://doi.org/10.5194/amt-18-1301-2025, 2025
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Methane is a potent greenhouse gas. Trustable detection and quantification of methane emissions at facility level are critical for identifying the largest sources and prioritizing them for repair. We provide a systematic analysis of several sources of uncertainty in drone-based methane emission surveys based on theoretical considerations and historical data sets. We provide guidelines for industry on how to avoid or minimize errors in drone-based methane emission quantification surveys.
Frank Hase, Paolo Castracane, Angelika Dehn, Omaira Elena García, David W. T. Griffith, Lukas Heizmann, Nicholas B. Jones, Tomi Karppinen, Rigel Kivi, Martine de Mazière, Justus Notholt, and Mahesh Kumar Sha
Atmos. Meas. Tech., 18, 1257–1267, https://doi.org/10.5194/amt-18-1257-2025, https://doi.org/10.5194/amt-18-1257-2025, 2025
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The primary measurement result delivered by a Fourier transform spectrometer is an interferogram, and the spectrum required for further analysis needs to be calculated from the interferogram by Fourier analysis. The paper deals with technical aspects of this process and shows how the reconstruction of the spectrum can be optimized.
Richard Eastes, J. Scott Evans, Quan Gan, William McClintock, and Jerry Lumpe
Atmos. Meas. Tech., 18, 921–928, https://doi.org/10.5194/amt-18-921-2025, https://doi.org/10.5194/amt-18-921-2025, 2025
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Temperature is essential to understanding the thermosphere. Most temperature measurements have been indirect or had large uncertainties, especially in the lower-middle thermosphere, where data are rarely available. Since October 2018, NASA’s GOLD mission has produced disk images of neutral temperatures near 160 km at locations over the Americas and Atlantic Ocean. This paper discusses both temperature retrieval techniques and issues in interpreting GOLD’s images of thermospheric temperatures.
Sanjeevani Panditharatne, Helen Brindley, Caroline Cox, Richard Siddans, Jonathan Murray, Laura Warwick, and Stuart Fox
Atmos. Meas. Tech., 18, 717–735, https://doi.org/10.5194/amt-18-717-2025, https://doi.org/10.5194/amt-18-717-2025, 2025
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Observations from the upcoming European Space Agency’s Far-Infrared Outgoing Radiation Understanding and Monitoring (FORUM) satellite are theorised to be highly sensitive to distributions of water vapour within Earth’s atmosphere. We exploit this sensitivity and extend the Infrared Microwave Sounding retrieval scheme for use on observations from FORUM. This scheme is evaluated on both simulated and observed measurements and shows good agreement with references of the atmospheric state.
Kelley C. Wells, Dylan B. Millet, Jared F. Brewer, Vivienne H. Payne, Karen E. Cady-Pereira, Rick Pernak, Susan Kulawik, Corinne Vigouroux, Nicholas Jones, Emmanuel Mahieu, Maria Makarova, Tomoo Nagahama, Ivan Ortega, Mathias Palm, Kimberly Strong, Matthias Schneider, Dan Smale, Ralf Sussmann, and Minqiang Zhou
Atmos. Meas. Tech., 18, 695–716, https://doi.org/10.5194/amt-18-695-2025, https://doi.org/10.5194/amt-18-695-2025, 2025
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Atmospheric volatile organic compounds (VOCs) affect both air quality and climate. Satellite measurements can help us to assess and predict their global impacts. We present new decadal (2012–2023) measurements of four key VOCs – methanol, ethene, ethyne, and hydrogen cyanide (HCN) – from the Cross-track Infrared Sounder. The measurements reflect emissions from major forests, wildfires, and industry and provide new information to advance understanding of these sources and their changes over time.
Otto Lamminpää, Jouni Susiluoto, Jonathan Hobbs, James McDuffie, Amy Braverman, and Houman Owhadi
Atmos. Meas. Tech., 18, 673–694, https://doi.org/10.5194/amt-18-673-2025, https://doi.org/10.5194/amt-18-673-2025, 2025
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We develop and demonstrate a fast forward function emulator for remote sensing of greenhouse gases. These forward functions are computationally expensive to evaluate, and as such the key challenge for many satellite missions in their data processing is the time used in these evaluations. Our method is fast and accurate enough, less than 1 % relative error, so that it could be safely used in operational processing.
Alistair Bell, Eric Sauvageat, Gunter Stober, Klemens Hocke, and Axel Murk
Atmos. Meas. Tech., 18, 555–567, https://doi.org/10.5194/amt-18-555-2025, https://doi.org/10.5194/amt-18-555-2025, 2025
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Hardware and software developments have been made on a 22 GHz microwave radiometer for the measurement of middle-atmospheric water vapour near Bern, Switzerland. Previous measurements dating back to 2010 have been re-calibrated and an improved optimal estimation retrieval performed on these measurements, giving a 13-year dataset. Measurements made with new and improved instrumental hardware are used to correct previous measurements, which show better agreement than the non-corrected dataset.
Alexandre Danjou, Grégoire Broquet, Andrew Schuh, François-Marie Bréon, and Thomas Lauvaux
Atmos. Meas. Tech., 18, 533–554, https://doi.org/10.5194/amt-18-533-2025, https://doi.org/10.5194/amt-18-533-2025, 2025
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We study the capacity of XCO2 spaceborne imagery to estimate urban CO2 emissions with synthetic data. We define automatic and standard methods and objective criteria for image selection. The wind variability and urban emission budget guide the emission estimation error. Images with low wind variability and high urban emissions account for 47 % of images and give a bias in the emission estimation of −7 % and a spread of 56 %. Other images give a bias of −31 % and a spread of 99 %.
Yiguo Pang, Longfei Tian, Denghui Hu, Shuang Gao, and Guohua Liu
Atmos. Meas. Tech., 18, 455–470, https://doi.org/10.5194/amt-18-455-2025, https://doi.org/10.5194/amt-18-455-2025, 2025
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The spatial adjacency of methane point sources can result in plume overlapping, presenting challenges for quantification from space. A separation and quantification method combining the Gaussian plume model and the integrated mass enhancement method is proposed. A modern parameter estimation technique is introduced to separate the overlapping plumes from satellite observations. The proposed method is evaluated with synthesized observations and real satellite observations.
Michael Weimer, Michael Hilker, Stefan Noël, Max Reuter, Michael Buchwitz, Blanca Fuentes Andrade, Rüdiger Lang, Bernd Sierk, Yasjka Meijer, Heinrich Bovensmann, John P. Burrows, and Hartmut Bösch
EGUsphere, https://doi.org/10.5194/egusphere-2024-3857, https://doi.org/10.5194/egusphere-2024-3857, 2025
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Optical detectors have a maximum signal (saturation). Exceedance means that the measurement has to be discarded. We investigate where saturation will occur for the future European satellite mission dedicated to CO2 Monitoring (CO2M) and strategies to avoid saturation. It impacts coverage and precision, both important for estimation of local CO2 emissions. We find that taking two pictures per sampling should be sufficient to avoid saturation for CO2M with some impact on the CO2 precision.
Maximilian Reuter, Michael Hilker, Stefan Noël, Antonio Di Noia, Michael Weimer, Oliver Schneising, Michael Buchwitz, Heinrich Bovensmann, John P. Burrows, Hartmut Bösch, and Ruediger Lang
Atmos. Meas. Tech., 18, 241–264, https://doi.org/10.5194/amt-18-241-2025, https://doi.org/10.5194/amt-18-241-2025, 2025
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Carbon dioxide (CO2) and methane (CH4) are the main anthropogenic greenhouse gases. The European Copernicus CO2 monitoring satellite mission CO2M will provide measurements of their atmospheric concentrations, but the accuracy requirements are demanding and conventional retrieval methods computationally expensive. We present a new retrieval algorithm based on artificial neural networks that has the potential to meet the stringent requirements of the CO2M mission with minimal computational effort.
Peter Somkuti, Greg M. McGarragh, Christopher O'Dell, Antonio Di Noia, Leif Vogel, Sean Crowell, Lesley E. Ott, and Hartmut Bösch
Atmos. Meas. Tech. Discuss., https://doi.org/10.5194/amt-2024-145, https://doi.org/10.5194/amt-2024-145, 2025
Revised manuscript accepted for AMT
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In space-based estimates of atmospheric methane concentrations, one can often observe biases that look like imprints of surface features. We performed realistic simulation experiments and find the root cause to be unaccounted aerosols. Since good knowledge of aerosols is difficult to achieve for operational science data processing, we conclude that a comprehensive surface bias correction scheme is highly important for missions utilizing the 2.3 µm spectral band for methane retrievals.
Luis Guanter, Jack Warren, Mark Omara, Apisada Chulakadabba, Javier Roger, Maryann Sargent, Jonathan E. Franklin, Steven C. Wofsy, and Ritesh Gautam
EGUsphere, https://doi.org/10.5194/egusphere-2024-3577, https://doi.org/10.5194/egusphere-2024-3577, 2025
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This study presents a data processing scheme for the detection and quantification of methane emissions using the MethaneAIR airborne spectrometer. We show that the proposed methods enable the detection of smaller plumes than other existing methods, and that improves the potential of MethaneAIR to survey methane point sources across large regions
Xiaoyi Zhao, Vitali Fioletov, Debora Griffin, Chris McLinden, Ralf Staebler, Cristian Mihele, Kevin Strawbridge, Jonathan Davies, Ihab Abboud, Sum Chi Lee, Alexander Cede, Martin Tiefengraber, and Robert Swap
Atmos. Meas. Tech., 17, 6889–6912, https://doi.org/10.5194/amt-17-6889-2024, https://doi.org/10.5194/amt-17-6889-2024, 2024
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This study explores differences between remote sensing and in situ instruments in terms of their vertical, horizontal, and temporal sampling differences. Understanding and resolving these differences are critical for future analyses linking satellite, ground-based remote sensing, and in situ observations in air quality monitoring. It shows that the meteorological conditions (wind directions, speed, and boundary layer conditions) will strongly affect the agreement between the two measurements.
Leon Kuhn, Steffen Beirle, Sergey Osipov, Andrea Pozzer, and Thomas Wagner
Atmos. Meas. Tech., 17, 6485–6516, https://doi.org/10.5194/amt-17-6485-2024, https://doi.org/10.5194/amt-17-6485-2024, 2024
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This paper presents a new machine learning model that allows us to compute NO2 concentration profiles from satellite observations. A neural network was trained on synthetic data from the regional chemistry and transport model WRF-Chem. This is the first model of its kind. We present a thorough model validation study, covering various seasons and regions of the world.
Swathi Maratt Satheesan, Kai-Uwe Eichmann, John P. Burrows, Mark Weber, Ryan Stauffer, Anne M. Thompson, and Debra Kollonige
Atmos. Meas. Tech., 17, 6459–6484, https://doi.org/10.5194/amt-17-6459-2024, https://doi.org/10.5194/amt-17-6459-2024, 2024
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CHORA, an advanced cloud convective differential technique, enhances the accuracy of tropospheric-ozone retrievals. Unlike the traditional Pacific cloud reference sector scheme, CHORA introduces a local-cloud reference sector and an alternative approach (CLCT) for precision. Analysing monthly averaged TROPOMI data from 2018 to 2022 and validating with SHADOZ ozonesonde data, CLCT outperforms other methods and so is the preferred choice, especially in future geostationary satellite missions.
Minqiang Zhou, Pucai Wang, Bart Dils, Bavo Langerock, Geoff Toon, Christian Hermans, Weidong Nan, Qun Cheng, and Martine De Mazière
Atmos. Meas. Tech., 17, 6385–6396, https://doi.org/10.5194/amt-17-6385-2024, https://doi.org/10.5194/amt-17-6385-2024, 2024
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Solar absorption spectra near 2967 cm−1 recorded by a ground-based FTIR with a high spectral resolution of 0.0035 cm-1 are applied to retrieve C3H8 columns for the first time in Xianghe, China, within the NDACC-IRWG. The mean and standard deviation of the C3H8 columns are 1.80 ± 0.81 (1σ) × 1015 molec. cm-2. Good correlations are found between C3H8 and other non-methane hydrocarbons, such as C2H6 (R = 0.84) and C2H2 (R = 0.79), as well as between C3H8 and CO (R = 0.72).
Janek Gödeke, Andreas Richter, Kezia Lange, Peter Maaß, Hyunkee Hong, Hanlim Lee, and Junsung Park
EGUsphere, https://doi.org/10.5194/egusphere-2024-3145, https://doi.org/10.5194/egusphere-2024-3145, 2024
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The Korean Geostationary Environmental Monitoring Spectrometer (GEMS) monitors trace gases over Asia, e.g., NO2. GEMS provides hourly data, improving the time-resolution compared to the daily overpasses by other satellites. For the prediction of hourly surface NO2 over Korea from GEMS observations and meteorological data, this study shows that machine learning models benefit from this higher time-resolution. This is achieved by using observations from previous hours as additional inputs.
Farrer Owsley-Brown, Martin J. Wooster, Mark J. Grosvenor, and Yanan Liu
Atmos. Meas. Tech., 17, 6247–6264, https://doi.org/10.5194/amt-17-6247-2024, https://doi.org/10.5194/amt-17-6247-2024, 2024
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Landscape fires produce vast amounts of smoke, affecting the atmosphere locally and globally. Whether a fire is flaming or smouldering strongly impacts the rate at which smoke is produced as well as its composition. This study tested two methods to determine these combustion phases in laboratory fires and compared them to the smoke emitted. One of these methods improved estimates of smoke emission significantly. This suggests potential for improvement in global emission estimates.
Sora Seo, Pieter Valks, Ronny Lutz, Klaus-Peter Heue, Pascal Hedelt, Víctor Molina García, Diego Loyola, Hanlim Lee, and Jhoon Kim
Atmos. Meas. Tech., 17, 6163–6191, https://doi.org/10.5194/amt-17-6163-2024, https://doi.org/10.5194/amt-17-6163-2024, 2024
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In this study, we developed an advanced retrieval algorithm for tropospheric NO2 columns from geostationary satellite spectrometers and applied it to GEMS measurements. The DLR GEMS NO2 retrieval algorithm follows the heritage from previous and existing algorithms, but improved approaches are applied to reflect the specific features of geostationary satellites. The DLR GEMS NO2 retrievals demonstrate a good capability for monitoring diurnal variability with a high spatial resolution.
Theodore K. Koenig, François Hendrick, Douglas Kinnison, Christopher F. Lee, Michel Van Roozendael, and Rainer Volkamer
Atmos. Meas. Tech., 17, 5911–5934, https://doi.org/10.5194/amt-17-5911-2024, https://doi.org/10.5194/amt-17-5911-2024, 2024
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Atmospheric bromine destroys ozone, impacts oxidation capacity, and oxidizes mercury into its toxic form. We constrain bromine by remote sensing of BrO from a mountaintop. Previous measurements retrieved two to three pieces of information vertically; we apply new methods to get five and a half vertically and two more in time. We compare with aircraft measurements to validate the methods and look at variations in BrO over the Pacific.
Kavitha Mottungan, Chayan Roychoudhury, Vanessa Brocchi, Benjamin Gaubert, Wenfu Tang, Mohammad Amin Mirrezaei, John McKinnon, Yafang Guo, David W. T. Griffith, Dietrich G. Feist, Isamu Morino, Mahesh K. Sha, Manvendra K. Dubey, Martine De Mazière, Nicholas M. Deutscher, Paul O. Wennberg, Ralf Sussmann, Rigel Kivi, Tae-Young Goo, Voltaire A. Velazco, Wei Wang, and Avelino F. Arellano Jr.
Atmos. Meas. Tech., 17, 5861–5885, https://doi.org/10.5194/amt-17-5861-2024, https://doi.org/10.5194/amt-17-5861-2024, 2024
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A combination of data analysis techniques is introduced to separate local and regional influences on observed levels of carbon dioxide, carbon monoxide, and methane from an established ground-based remote sensing network. We take advantage of the covariations in these trace gases to identify the dominant type of sources driving these levels. Applying these methods in conjunction with existing approaches to other datasets can better address uncertainties in identifying sources and sinks.
Chia-Pang Kuo and Christian Kummerow
Atmos. Meas. Tech., 17, 5637–5653, https://doi.org/10.5194/amt-17-5637-2024, https://doi.org/10.5194/amt-17-5637-2024, 2024
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A small satellite about the size of a shoe box, named TEMPEST, carries only a microwave sensor and is designed to measure the water cycle of the Earth from space in an economical way compared with traditional satellites, which have additional infrared sensors. To overcome the limitation, extra infrared signals from GOES-R ABI are combined with TEMPEST microwave measurements. Compared with ground observations, improved humidity information is extracted from the merged TEMPEST and ABI signals.
Carley D. Fredrickson, Scott J. Janz, Lok N. Lamsal, Ursula A. Jongebloed, Joshua L. Laughner, and Joel A. Thornton
Atmos. Meas. Tech. Discuss., https://doi.org/10.5194/amt-2024-158, https://doi.org/10.5194/amt-2024-158, 2024
Revised manuscript accepted for AMT
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We present an analysis of high-resolution remote sensing measurements of nitrogen-containing trace gases emitted by wildfires. The measurements were made using an instrument on the NASA ER-2 aircraft in the summer of 2019. We find that time-resolved fire intensity is critical to quantify trace gas emissions over a fire’s entire lifespan. These findings have implications for improving air pollution forecasts downwind of wildfires using computer models of atmospheric chemistry and meteorology.
Mickaël Bacles, Jonathan Améric, and Vincent Guidard
EGUsphere, https://doi.org/10.5194/egusphere-2024-2941, https://doi.org/10.5194/egusphere-2024-2941, 2024
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Sulfur dioxide emitted during volcanic eruptions can be hazardous for aviation safety. A recent development aims at improving the forecasts of volcanic sulfur dioxide quantities made by the MOCAGE chemistry transport model. Both TROPOMI and IASI instruments are assimilated in the model. We focus on the eruption event of the La Soufrière Saint-Vincent volcano in April 2021. The combined assimilation of IASI and TROPOMI observations always leads to a better analyses and forecasts.
Christopher Chan Miller, Sébastien Roche, Jonas S. Wilzewski, Xiong Liu, Kelly Chance, Amir H. Souri, Eamon Conway, Bingkun Luo, Jenna Samra, Jacob Hawthorne, Kang Sun, Carly Staebell, Apisada Chulakadabba, Maryann Sargent, Joshua S. Benmergui, Jonathan E. Franklin, Bruce C. Daube, Yang Li, Joshua L. Laughner, Bianca C. Baier, Ritesh Gautam, Mark Omara, and Steven C. Wofsy
Atmos. Meas. Tech., 17, 5429–5454, https://doi.org/10.5194/amt-17-5429-2024, https://doi.org/10.5194/amt-17-5429-2024, 2024
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MethaneSAT is an upcoming satellite mission designed to monitor methane emissions from the oil and gas (O&G) industry globally. Here, we present observations from the first flight campaign of MethaneAIR, a MethaneSAT-like instrument mounted on an aircraft. MethaneAIR can map methane with high precision and accuracy over a typically sized oil and gas basin (~200 km2) in a single flight. This paper demonstrates the capability of the upcoming satellite to routinely track global O&G emissions.
Matthieu Dogniaux and Cyril Crevoisier
Atmos. Meas. Tech., 17, 5373–5396, https://doi.org/10.5194/amt-17-5373-2024, https://doi.org/10.5194/amt-17-5373-2024, 2024
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Many CO2-observing satellite concepts, with very different design choices and trade-offs, are expected to be put into orbit during the upcoming decade. This work uses numerical simulations to explore the impact of critical design parameters on the performance of upcoming CO2-observing satellite concepts.
Francesca Vittorioso, Vincent Guidard, and Nadia Fourrié
Atmos. Meas. Tech., 17, 5279–5299, https://doi.org/10.5194/amt-17-5279-2024, https://doi.org/10.5194/amt-17-5279-2024, 2024
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The future Meteosat Third Generation Infrared Sounder (MTG-IRS) will represent a major innovation for the monitoring of the chemical state of the atmosphere. MTG-IRS will have the advantage of being based on a geostationary platform and acquiring data with a high temporal frequency. This work aims to evaluate its potential impact over Europe within a chemical transport model (MOCAGE). The results indicate that the assimilation of these data always has a positive impact on ozone analysis.
Matthias Schneider, Kinya Toride, Farahnaz Khosrawi, Frank Hase, Benjamin Ertl, Christopher J. Diekmann, and Kei Yoshimura
Atmos. Meas. Tech., 17, 5243–5259, https://doi.org/10.5194/amt-17-5243-2024, https://doi.org/10.5194/amt-17-5243-2024, 2024
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Despite its importance for extreme weather and climate feedbacks, atmospheric convection is not well constrained. This study assesses the potential of novel tropospheric water vapour isotopologue satellite observations for improving the analyses of convective events. We find that the impact of the isotopologues is small for stable atmospheric conditions but significant for unstable conditions, which have the strongest societal impacts (e.g. storms and flooding).
Mengyao Liu, Ronald van der A, Michiel van Weele, Lotte Bryan, Henk Eskes, Pepijn Veefkind, Yongxue Liu, Xiaojuan Lin, Jos de Laat, and Jieying Ding
Atmos. Meas. Tech., 17, 5261–5277, https://doi.org/10.5194/amt-17-5261-2024, https://doi.org/10.5194/amt-17-5261-2024, 2024
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A new divergence method was developed and applied to estimate methane emissions from TROPOMI observations over the Middle East, where it is typically challenging for a satellite to measure methane due to its complicated orography and surface albedo. Our results show the potential of TROPOMI to quantify methane emissions from various sources rather than big emitters from space after objectively excluding the artifacts in the retrieval.
Yujin J. Oak, Daniel J. Jacob, Nicholas Balasus, Laura H. Yang, Heesung Chong, Junsung Park, Hanlim Lee, Gitaek T. Lee, Eunjo S. Ha, Rokjin J. Park, Hyeong-Ahn Kwon, and Jhoon Kim
Atmos. Meas. Tech., 17, 5147–5159, https://doi.org/10.5194/amt-17-5147-2024, https://doi.org/10.5194/amt-17-5147-2024, 2024
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We present an improved NO2 product from GEMS by calibrating it to TROPOMI using machine learning and by reprocessing both satellite products to adopt common NO2 profiles. Our corrected GEMS product combines the high data density of GEMS with the accuracy of TROPOMI, supporting the combined use for analyses of East Asia air quality including emissions and chemistry. This method can be extended to other species and geostationary satellites including TEMPO and Sentinel-4.
Xianzhong Duan, Ming Chang, Guotong Wu, Suping Situ, Shengjie Zhu, Qi Zhang, Yibo Huangfu, Weiwen Wang, Weihua Chen, Bin Yuan, and Xuemei Wang
Atmos. Meas. Tech., 17, 4065–4079, https://doi.org/10.5194/amt-17-4065-2024, https://doi.org/10.5194/amt-17-4065-2024, 2024
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Accurately estimating biogenic volatile organic compound (BVOC) emissions in forest ecosystems has been challenging. This research presents a framework that utilizes drone-based lidar, photogrammetry, and image recognition technologies to identify plant species and estimate BVOC emissions. The largest cumulative isoprene emissions were found in the Myrtaceae family, while those of monoterpenes were from the Rubiaceae family.
Fengxin Xie, Tao Ren, Changying Zhao, Yuan Wen, Yilei Gu, Minqiang Zhou, Pucai Wang, Kei Shiomi, and Isamu Morino
Atmos. Meas. Tech., 17, 3949–3967, https://doi.org/10.5194/amt-17-3949-2024, https://doi.org/10.5194/amt-17-3949-2024, 2024
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This study demonstrates a new machine learning approach to efficiently and accurately estimate atmospheric carbon dioxide levels from satellite data. Rather than using traditional complex physics-based retrieval methods, neural network models are trained on simulated data to rapidly predict CO2 concentrations directly from satellite spectral measurements.
Steffen Beirle and Thomas Wagner
Atmos. Meas. Tech., 17, 3439–3453, https://doi.org/10.5194/amt-17-3439-2024, https://doi.org/10.5194/amt-17-3439-2024, 2024
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We present a new method for estimating emissions and lifetimes for nitrogen oxides emitted from large cities by using satellite NO2 observations combined with wind fields. The estimate is based on the simultaneous evaluation of the downwind plumes for opposing wind directions. This allows us to derive seasonal mean emissions and lifetimes for 100 cities around the globe.
Qiurun Yu, Dylan Jervis, and Yi Huang
Atmos. Meas. Tech., 17, 3347–3366, https://doi.org/10.5194/amt-17-3347-2024, https://doi.org/10.5194/amt-17-3347-2024, 2024
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This study estimated the effects of aerosols on GHGSat satellite methane retrieval and investigated the performance of simultaneously retrieving aerosol and methane information using a multi-angle viewing method. Results suggested that the performance of GHGSat methane retrieval improved when aerosols were considered, and the multi-angle viewing method is insensitive to the satellite angle setting. This performance assessment is useful for improving future GHGSat-like instruments.
Zhonghua He, Ling Gao, Miao Liang, and Zhao-Cheng Zeng
Atmos. Meas. Tech., 17, 2937–2956, https://doi.org/10.5194/amt-17-2937-2024, https://doi.org/10.5194/amt-17-2937-2024, 2024
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Using Gaofen-5B satellite data, this study detected 93 methane plume events from 32 coal mines in Shanxi, China, with emission rates spanning from 761.78 ± 185.00 to 12729.12 ± 4658.13 kg h-1, showing significant variability among sources. This study highlights Gaofen-5B’s capacity for monitoring large methane point sources, offering valuable support in reducing greenhouse gas emissions.
Heesung Chong, Gonzalo González Abad, Caroline R. Nowlan, Christopher Chan Miller, Alfonso Saiz-Lopez, Rafael P. Fernandez, Hyeong-Ahn Kwon, Zolal Ayazpour, Huiqun Wang, Amir H. Souri, Xiong Liu, Kelly Chance, Ewan O'Sullivan, Jhoon Kim, Ja-Ho Koo, William R. Simpson, François Hendrick, Richard Querel, Glen Jaross, Colin Seftor, and Raid M. Suleiman
Atmos. Meas. Tech., 17, 2873–2916, https://doi.org/10.5194/amt-17-2873-2024, https://doi.org/10.5194/amt-17-2873-2024, 2024
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We present a new bromine monoxide (BrO) product derived using radiances measured from OMPS-NM on board the Suomi-NPP satellite. This product provides nearly a decade of global stratospheric and tropospheric column retrievals, a feature that is currently rare in publicly accessible datasets. Both stratospheric and tropospheric columns from OMPS-NM demonstrate robust performance, exhibiting good agreement with ground-based observations collected at three stations (Lauder, Utqiagvik, and Harestua).
Norbert Glatthor, Thomas von Clarmann, Bernd Funke, Maya García-Comas, Udo Grabowski, Michael Höpfner, Sylvia Kellmann, Michael Kiefer, Alexandra Laeng, Andrea Linden, Manuel López-Puertas, and Gabriele P. Stiller
Atmos. Meas. Tech., 17, 2849–2871, https://doi.org/10.5194/amt-17-2849-2024, https://doi.org/10.5194/amt-17-2849-2024, 2024
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We present global atmospheric methane (CH4) and nitrous oxide (N2O) distributions retrieved from measurements of the MIPAS instrument on board the Environmental Satellite (Envisat) during 2002 to 2012. Monitoring of these gases is of scientific interest because both of them are strong greenhouse gases. We analyze the latest, improved version of calibrated MIPAS measurements. Further, we apply a new retrieval scheme leading to an improved CH4 and N2O data product .
Matthieu Dogniaux, Joannes D. Maasakkers, Daniel J. Varon, and Ilse Aben
Atmos. Meas. Tech., 17, 2777–2787, https://doi.org/10.5194/amt-17-2777-2024, https://doi.org/10.5194/amt-17-2777-2024, 2024
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We analyze Landsat 8 (L8) and Sentinel-2B (S-2B) observations of the 2022 Nord Stream 2 methane leak and show how challenging this case is for usual data analysis methods. We provide customized calibrations for this Nord Stream 2 case and assess that no firm conclusion can be drawn from L8 or S-2B single overpasses. However, if we opportunistically assume that L8 and S-2B results are independent, we find an averaged L8 and S-2B combined methane leak rate of 502 ± 464 t h−1.
Jack H. Bruno, Dylan Jervis, Daniel J. Varon, and Daniel J. Jacob
Atmos. Meas. Tech., 17, 2625–2636, https://doi.org/10.5194/amt-17-2625-2024, https://doi.org/10.5194/amt-17-2625-2024, 2024
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Methane is a potent greenhouse gas and a current high-priority target for short- to mid-term climate change mitigation. Detection of individual methane emitters from space has become possible in recent years, and the volume of data for this task has been rapidly growing, outpacing processing capabilities. We introduce an automated approach, U-Plume, which can detect and quantify emissions from individual methane sources in high-spatial-resolution satellite data.
Anna Vaughan, Gonzalo Mateo-García, Luis Gómez-Chova, Vít Růžička, Luis Guanter, and Itziar Irakulis-Loitxate
Atmos. Meas. Tech., 17, 2583–2593, https://doi.org/10.5194/amt-17-2583-2024, https://doi.org/10.5194/amt-17-2583-2024, 2024
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Methane is a potent greenhouse gas that has been responsible for around 25 % of global warming since the industrial revolution. Consequently identifying and mitigating methane emissions comprise an important step in combating the climate crisis. We develop a new deep learning model to automatically detect methane plumes from satellite images and demonstrate that this can be applied to monitor large methane emissions resulting from the oil and gas industry.
Stefan Noël, Michael Buchwitz, Michael Hilker, Maximilian Reuter, Michael Weimer, Heinrich Bovensmann, John P. Burrows, Hartmut Bösch, and Ruediger Lang
Atmos. Meas. Tech., 17, 2317–2334, https://doi.org/10.5194/amt-17-2317-2024, https://doi.org/10.5194/amt-17-2317-2024, 2024
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FOCAL-CO2M is one of the three operational retrieval algorithms which will be used to derive XCO2 and XCH4 from measurements of the forthcoming European CO2M mission. We present results of applications of FOCAL-CO2M to simulated spectra, from which confidence is gained that the algorithm is able to fulfil the challenging requirements on systematic errors for the CO2M mission (spatio-temporal bias ≤ 0.5 ppm for XCO2 and ≤ 5 ppb for XCH4).
Marvin Knapp, Ralph Kleinschek, Sanam N. Vardag, Felix Külheim, Helge Haveresch, Moritz Sindram, Tim Siegel, Bruno Burger, and André Butz
Atmos. Meas. Tech., 17, 2257–2275, https://doi.org/10.5194/amt-17-2257-2024, https://doi.org/10.5194/amt-17-2257-2024, 2024
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Imaging carbon dioxide (CO2) plumes of anthropogenic sources from planes and satellites has proven valuable for detecting emitters and monitoring climate mitigation efforts. We present the first images of CO2 plumes taken with a ground-based spectral camera, observing a coal-fired power plant as a validation target. We develop a technique to find the source emission strength with an hourly resolution, which reasonably agrees with the expected emissions under favorable conditions.
Karl Voglmeier, Voltaire A. Velazco, Luca Egli, Julian Gröbner, Alberto Redondas, and Wolfgang Steinbrecht
Atmos. Meas. Tech., 17, 2277–2294, https://doi.org/10.5194/amt-17-2277-2024, https://doi.org/10.5194/amt-17-2277-2024, 2024
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Comparison between total ozone column (TOC) measurements from ground-based Dobson and Brewer spectrophotometers generally reveals seasonally varying differences of a few percent. This study recommends a new TOC retrieval approach, which effectively eliminates these seasonally varying differences by applying new ozone absorption cross sections, appropriate slit functions for the Dobson instrument, and climatological values for the effective ozone temperature.
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Short summary
Currently, measurement of methane from the TROPOMI satellite is biased with respect to surface reflectance. This study demonstrates a new method of correcting for this bias on a seasonal timescale to allow for differences in surface reflectance in areas of intense agriculture where growing seasons may introduce a reflectance bias. We have successfully implemented this technique in the Denver–Julesburg basin, where agriculture and methane extraction infrastructure is often co-located.
Currently, measurement of methane from the TROPOMI satellite is biased with respect to surface...
