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Articles | Volume 14, issue 19
Atmos. Chem. Phys., 14, 10565–10588, 2014
https://doi.org/10.5194/acp-14-10565-2014
© Author(s) 2014. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Atmos. Chem. Phys., 14, 10565–10588, 2014
https://doi.org/10.5194/acp-14-10565-2014
© Author(s) 2014. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Research article 09 Oct 2014
Research article | 09 Oct 2014
First estimates of global free-tropospheric NO2 abundances derived using a cloud-slicing technique applied to satellite observations from the Aura Ozone Monitoring Instrument (OMI)
S. Choi et al.
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The NASA standard nitrogen dioxide (NO2) version 4.0 product for OMI Aura incorporates the most salient improvements. It represents the first global satellite trace gas retrieval with OMI–MODIS synergy accounting for surface reflectance anisotropy in cloud and NO2 retrievals. Improved spectral fitting procedures for NO2 and oxygen dimer (for cloud) retrievals and reliance on high-resolution field-of-view-specific input information for NO2 and cloud retrievals help enhance the NO2 data quality.
Eloise A. Marais, John F. Roberts, Robert G. Ryan, Henk Eskes, K. Folkert Boersma, Sungyeon Choi, Joanna Joiner, Nader Abuhassan, Alberto Redondas, Michel Grutter, Alexander Cede, Laura Gomez, and Monica Navarro-Comas
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Nitrogen oxides in the upper troposphere have a profound influence on the global troposphere, though observations there are exceedingly rare. We apply cloud-slicing to high spatial resolution TROPOMI total columns of nitrogen dioxide (NO2) to derive near-global observations of upper tropospheric NO2 concentrations and show consistency with existing datasets. These data offer tremendous potential to address knowledge gaps in this oft under-appreciated portion of the atmosphere.
Jiayue Huang, Lyatt Jaeglé, Qianjie Chen, Becky Alexander, Tomás Sherwen, Mat J. Evans, Nicolas Theys, and Sungyeon Choi
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Large-scale enhancements of tropospheric BrO and the depletion of surface ozone are often observed in the springtime Arctic. Here, we use a chemical transport model to examine the role of sea salt aerosol from blowing snow in explaining these phenomena. We find that our simulation can account for the spatiotemporal variability of satellite observations of BrO. However, the model has difficulty in producing the magnitude of observed ozone depletion events.
Sungyeon Choi, Lok N. Lamsal, Melanie Follette-Cook, Joanna Joiner, Nickolay A. Krotkov, William H. Swartz, Kenneth E. Pickering, Christopher P. Loughner, Wyat Appel, Gabriele Pfister, Pablo E. Saide, Ronald C. Cohen, Andrew J. Weinheimer, and Jay R. Herman
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The US EPA reports a steady decrease in nitrogen oxide (NOx) emissions from fuel combustion over the 2005–2017 period, while satellite observations show a leveling off after 2009, suggesting emission reductions and related air quality gains have halted. We show the sustained decrease in NOx emissions is in fact consistent with observed trends in surface NO2 and ozone concentrations and that the flattening of the satellite trend reflects a growing influence from the non-anthropogenic background.
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Lok N. Lamsal, Nickolay A. Krotkov, Alexander Vasilkov, Sergey Marchenko, Wenhan Qin, Eun-Su Yang, Zachary Fasnacht, Joanna Joiner, Sungyeon Choi, David Haffner, William H. Swartz, Bradford Fisher, and Eric Bucsela
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The NASA standard nitrogen dioxide (NO2) version 4.0 product for OMI Aura incorporates the most salient improvements. It represents the first global satellite trace gas retrieval with OMI–MODIS synergy accounting for surface reflectance anisotropy in cloud and NO2 retrievals. Improved spectral fitting procedures for NO2 and oxygen dimer (for cloud) retrievals and reliance on high-resolution field-of-view-specific input information for NO2 and cloud retrievals help enhance the NO2 data quality.
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Can Li, Nickolay A. Krotkov, Peter J. T. Leonard, Simon Carn, Joanna Joiner, Robert J. D. Spurr, and Alexander Vasilkov
Atmos. Meas. Tech., 13, 6175–6191, https://doi.org/10.5194/amt-13-6175-2020, https://doi.org/10.5194/amt-13-6175-2020, 2020
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Arman Pouyaei, Yunsoo Choi, Jia Jung, Bavand Sadeghi, and Chul Han Song
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Sarah A. Strode, James S. Wang, Michael Manyin, Bryan Duncan, Ryan Hossaini, Christoph A. Keller, Sylvia E. Michel, and James W. C. White
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Junjie Liu, Latha Baskaran, Kevin Bowman, David Schimel, A. Anthony Bloom, Nicholas C. Parazoo, Tomohiro Oda, Dustin Carroll, Dimitris Menemenlis, Joanna Joiner, Roisin Commane, Bruce Daube, Lucianna V. Gatii, Kathryn McKain, John Miller, Britton B. Stephens, Colm Sweeney, and Steven Wofsy
Earth Syst. Sci. Data Discuss., https://doi.org/10.5194/essd-2020-123, https://doi.org/10.5194/essd-2020-123, 2020
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Jiayue Huang, Lyatt Jaeglé, Qianjie Chen, Becky Alexander, Tomás Sherwen, Mat J. Evans, Nicolas Theys, and Sungyeon Choi
Atmos. Chem. Phys., 20, 7335–7358, https://doi.org/10.5194/acp-20-7335-2020, https://doi.org/10.5194/acp-20-7335-2020, 2020
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Large-scale enhancements of tropospheric BrO and the depletion of surface ozone are often observed in the springtime Arctic. Here, we use a chemical transport model to examine the role of sea salt aerosol from blowing snow in explaining these phenomena. We find that our simulation can account for the spatiotemporal variability of satellite observations of BrO. However, the model has difficulty in producing the magnitude of observed ozone depletion events.
Sungyeon Choi, Lok N. Lamsal, Melanie Follette-Cook, Joanna Joiner, Nickolay A. Krotkov, William H. Swartz, Kenneth E. Pickering, Christopher P. Loughner, Wyat Appel, Gabriele Pfister, Pablo E. Saide, Ronald C. Cohen, Andrew J. Weinheimer, and Jay R. Herman
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Vitali Fioletov, Chris A. McLinden, Debora Griffin, Nicolas Theys, Diego G. Loyola, Pascal Hedelt, Nickolay A. Krotkov, and Can Li
Atmos. Chem. Phys., 20, 5591–5607, https://doi.org/10.5194/acp-20-5591-2020, https://doi.org/10.5194/acp-20-5591-2020, 2020
Alexander Vasilkov, Nickolay Krotkov, Eun-Su Yang, Lok Lamsal, Joanna Joiner, Patricia Castellanos, Zachary Fasnacht, and Robert Spurr
Atmos. Meas. Tech. Discuss., https://doi.org/10.5194/amt-2019-458, https://doi.org/10.5194/amt-2019-458, 2020
Revised manuscript under review for AMT
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To explicitly account for aerosol effects in the OMI cloud and nitrogen dioxide algorithms,
we use a model of aerosol optical properties from a global aerosol
assimilation system and radiative transfer computations. We also account for anisotropic
reflection of Earth's surface. Our aerosol correction increases
the tropospheric nitrogen dioxide retrievals by 20 % for polluted areas and allows to reduce
the known biases in the retrievals.
Julie M. Nicely, Bryan N. Duncan, Thomas F. Hanisco, Glenn M. Wolfe, Ross J. Salawitch, Makoto Deushi, Amund S. Haslerud, Patrick Jöckel, Béatrice Josse, Douglas E. Kinnison, Andrew Klekociuk, Michael E. Manyin, Virginie Marécal, Olaf Morgenstern, Lee T. Murray, Gunnar Myhre, Luke D. Oman, Giovanni Pitari, Andrea Pozzer, Ilaria Quaglia, Laura E. Revell, Eugene Rozanov, Andrea Stenke, Kane Stone, Susan Strahan, Simone Tilmes, Holger Tost, Daniel M. Westervelt, and Guang Zeng
Atmos. Chem. Phys., 20, 1341–1361, https://doi.org/10.5194/acp-20-1341-2020, https://doi.org/10.5194/acp-20-1341-2020, 2020
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Differences in methane lifetime among global models are large and poorly understood. We use a neural network method and simulations from the Chemistry Climate Model Initiative to quantify the factors influencing methane lifetime spread among models and variations over time. UV photolysis, tropospheric ozone, and nitrogen oxides drive large model differences, while the same factors plus specific humidity contribute to a decreasing trend in methane lifetime between 1980 and 2015.
Fei Liu, Bryan N. Duncan, Nickolay A. Krotkov, Lok N. Lamsal, Steffen Beirle, Debora Griffin, Chris A. McLinden, Daniel L. Goldberg, and Zifeng Lu
Atmos. Chem. Phys., 20, 99–116, https://doi.org/10.5194/acp-20-99-2020, https://doi.org/10.5194/acp-20-99-2020, 2020
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We present a novel method to infer CO2 emissions from individual power plants, based on satellite observations of co-emitted NO2. We find that the CO2 emissions estimated by our satellite-based method during 2005–2017 are in reasonable agreement with the CEMS measurements for US power plants. The broader implication of our methodology is that it has the potential to provide an additional constraint on CO2 emissions from power plants in regions of the world without reliable emissions accounting.
Zachary Fasnacht, Alexander Vasilkov, David Haffner, Wenhan Qin, Joanna Joiner, Nickolay Krotkov, Andrew M. Sayer, and Robert Spurr
Atmos. Meas. Tech., 12, 6749–6769, https://doi.org/10.5194/amt-12-6749-2019, https://doi.org/10.5194/amt-12-6749-2019, 2019
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The anisotropy of Earth's surface reflection plays an important role in satellite-based retrievals of cloud, aerosol, and trace gases. Most current ultraviolet and visible satellite retrievals utilize climatological surface reflectivity databases that do not account for surface anisotropy. The GLER concept was introduced to account for such features. Here we evaluate GLER for water surfaces by comparing with OMI measurements and show that it captures these surface anisotropy features.
Bradford L. Fisher, Nickolay A. Krotkov, Pawan K. Bhartia, Can Li, Simon A. Carn, Eric Hughes, and Peter J. T. Leonard
Atmos. Meas. Tech., 12, 5137–5153, https://doi.org/10.5194/amt-12-5137-2019, https://doi.org/10.5194/amt-12-5137-2019, 2019
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This article describes a new discrete wavelength algorithm, MS_SO2, which has been used operationally to retrieve global daily volcanic SO2 vertical column densities and the UV volcanic ash index from the Total Ozone Mapping Spectrometer (TOMS) data collected by NASA’s Nimbus-7 satellite from 1978 to 1991. We examine the sensitivity of the algorithm to the detection of SO2, evaluate potential sources of error and compare results from MS_SO2 with the Principal Component Analysis (PCA) algorithm.
Wenhan Qin, Zachary Fasnacht, David Haffner, Alexander Vasilkov, Joanna Joiner, Nickolay Krotkov, Bradford Fisher, and Robert Spurr
Atmos. Meas. Tech., 12, 3997–4017, https://doi.org/10.5194/amt-12-3997-2019, https://doi.org/10.5194/amt-12-3997-2019, 2019
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Satellite observations depend on Sun and view angles due to anisotropy of the Earth's atmosphere and surface reflection. But most of the ultraviolet and visible cloud, aerosol, and trace-gas algorithms utilize surface reflectivity databases that do not account for surface anisotropy. We create a surface database using the GLER concept which adequately accounts for surface anisotropy, validate it with independent satellite data, and provide a simple implementation to the current algorithms.
Rachel F. Silvern, Daniel J. Jacob, Loretta J. Mickley, Melissa P. Sulprizio, Katherine R. Travis, Eloise A. Marais, Ronald C. Cohen, Joshua L. Laughner, Sungyeon Choi, Joanna Joiner, and Lok N. Lamsal
Atmos. Chem. Phys., 19, 8863–8878, https://doi.org/10.5194/acp-19-8863-2019, https://doi.org/10.5194/acp-19-8863-2019, 2019
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The US EPA reports a steady decrease in nitrogen oxide (NOx) emissions from fuel combustion over the 2005–2017 period, while satellite observations show a leveling off after 2009, suggesting emission reductions and related air quality gains have halted. We show the sustained decrease in NOx emissions is in fact consistent with observed trends in surface NO2 and ozone concentrations and that the flattening of the satellite trend reflects a growing influence from the non-anthropogenic background.
Paul I. Palmer, Emily L. Wilson, Geronimo L. Villanueva, Giuliano Liuzzi, Liang Feng, Anthony J. DiGregorio, Jianping Mao, Lesley Ott, and Bryan Duncan
Atmos. Meas. Tech., 12, 2579–2594, https://doi.org/10.5194/amt-12-2579-2019, https://doi.org/10.5194/amt-12-2579-2019, 2019
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We describe the potential impact of a new, low-cost, portable ground instrument (the mini-LHR) that measures methane and carbon dioxide in the atmospheric column. This region is key in quantifying the global carbon budget but has geographical gaps in measurements left by ground-based networks and space-based observations. A deployment of 50 mini-LHRs would add new data products in the Amazon, the Arctic, and southern Asia and significantly improve knowledge of regional and global carbon budgets.
Yuekui Yang, Kerry Meyer, Galina Wind, Yaping Zhou, Alexander Marshak, Steven Platnick, Qilong Min, Anthony B. Davis, Joanna Joiner, Alexander Vasilkov, David Duda, and Wenying Su
Atmos. Meas. Tech., 12, 2019–2031, https://doi.org/10.5194/amt-12-2019-2019, https://doi.org/10.5194/amt-12-2019-2019, 2019
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The physical basis of the EPIC cloud product algorithms and an initial evaluation of their performance are presented. EPIC cloud products include cloud mask, effective height, and optical depth. Comparison with co-located retrievals from geosynchronous earth orbit (GEO) and low earth orbit (LEO) satellites shows that the algorithms are performing well and are consistent with theoretical expectations. These products are publicly available at the NASA Langley Atmospheric Sciences Data Center.
Cristen Adams, Chris A. McLinden, Mark W. Shephard, Nolan Dickson, Enrico Dammers, Jack Chen, Paul Makar, Karen E. Cady-Pereira, Naomi Tam, Shailesh K. Kharol, Lok N. Lamsal, and Nickolay A. Krotkov
Atmos. Chem. Phys., 19, 2577–2599, https://doi.org/10.5194/acp-19-2577-2019, https://doi.org/10.5194/acp-19-2577-2019, 2019
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We estimated how much carbon monoxide, ammonia, and nitrogen oxides were emitted in the smoke from the Fort McMurray Horse River wildfire using satellite data and air quality models. The fire emitted amounts of carbon monoxide that were similar to anthropogenic (human-caused) emissions for all of Alberta over a full year. We also estimated large amounts of ammonia and nitrogen oxides emitted from the fire. These results can be used to evaluate the performance of air quality forecasting models.
Huanxin Zhang, Jun Wang, Lorena Castro García, Jing Zeng, Connor Dennhardt, Yang Liu, and Nickolay A. Krotkov
Atmos. Chem. Phys., 19, 2165–2181, https://doi.org/10.5194/acp-19-2165-2019, https://doi.org/10.5194/acp-19-2165-2019, 2019
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OMU-based surface erythemal UV irradiance is compared with ground observations in the United States from 2005 to 2017. We reveal that the assumption of constant atmospheric conditions between OMI overpass time and local solar noon time may not fully represent the real atmosphere and the peaks of surface UV are not always at local solar noon because of cloud effects. Future geostationary satellites (e.g., TEMPO) would reduce sampling bias and improve trend analysis of surface UV estimate.
Eloise A. Marais, Daniel J. Jacob, Sungyeon Choi, Joanna Joiner, Maria Belmonte-Rivas, Ronald C. Cohen, Steffen Beirle, Lee T. Murray, Luke D. Schiferl, Viral Shah, and Lyatt Jaeglé
Atmos. Chem. Phys., 18, 17017–17027, https://doi.org/10.5194/acp-18-17017-2018, https://doi.org/10.5194/acp-18-17017-2018, 2018
Short summary
Short summary
We intercompare two new products of global upper tropospheric nitrogen dioxide (NO2) retrieved from the Ozone Monitoring Instrument (OMI). We evaluate these products with aircraft observations from NASA DC8 aircraft campaigns and interpret the useful information these products can provide about nitrogen oxides (NOx) in the global upper troposphere using the GEOS-Chem chemical transport model.
Fei Liu, Sungyeon Choi, Can Li, Vitali E. Fioletov, Chris A. McLinden, Joanna Joiner, Nickolay A. Krotkov, Huisheng Bian, Greet Janssens-Maenhout, Anton S. Darmenov, and Arlindo M. da Silva
Atmos. Chem. Phys., 18, 16571–16586, https://doi.org/10.5194/acp-18-16571-2018, https://doi.org/10.5194/acp-18-16571-2018, 2018
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Sulfur dioxide measurements from space have been used to detect emissions from large sources. We developed a new emission inventory by combining the satellite-based emission estimates and the conventional bottom-up inventory for smaller sources. The new inventory improves the model agreement with in situ observations and offers the possibility of rapid updates to emissions.
Jeffrey A. Geddes, Randall V. Martin, Eric J. Bucsela, Chris A. McLinden, and Daniel J. M. Cunningham
Atmos. Meas. Tech., 11, 6271–6287, https://doi.org/10.5194/amt-11-6271-2018, https://doi.org/10.5194/amt-11-6271-2018, 2018
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This paper describes an approach for separating the stratospheric and tropospheric contributions in geostationary observations of nitrogen dioxide from the upcoming TEMPO instrument. We find minimal impact of the limited field of observation compared to previous low-Earth-observing systems with global coverage. We find that continued development of low-Earth-orbit retrievals will benefit geostationary data by providing important context outside the field of regard.
Arlene M. Fiore, Emily V. Fischer, George P. Milly, Shubha Pandey Deolal, Oliver Wild, Daniel A. Jaffe, Johannes Staehelin, Olivia E. Clifton, Dan Bergmann, William Collins, Frank Dentener, Ruth M. Doherty, Bryan N. Duncan, Bernd Fischer, Stefan Gilge, Peter G. Hess, Larry W. Horowitz, Alexandru Lupu, Ian A. MacKenzie, Rokjin Park, Ludwig Ries, Michael G. Sanderson, Martin G. Schultz, Drew T. Shindell, Martin Steinbacher, David S. Stevenson, Sophie Szopa, Christoph Zellweger, and Guang Zeng
Atmos. Chem. Phys., 18, 15345–15361, https://doi.org/10.5194/acp-18-15345-2018, https://doi.org/10.5194/acp-18-15345-2018, 2018
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We demonstrate a proof-of-concept approach for applying northern midlatitude mountaintop peroxy acetyl nitrate (PAN) measurements and a multi-model ensemble during April to constrain the influence of continental-scale anthropogenic precursor emissions on PAN. Our findings imply a role for carefully coordinated multi-model ensembles in helping identify observations for discriminating among widely varying (and poorly constrained) model responses of atmospheric constituents to changes in emissions.
Yao Zhang, Joanna Joiner, Seyed Hamed Alemohammad, Sha Zhou, and Pierre Gentine
Biogeosciences, 15, 5779–5800, https://doi.org/10.5194/bg-15-5779-2018, https://doi.org/10.5194/bg-15-5779-2018, 2018
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Using satellite reflectance measurements and a machine learning algorithm, we generated a new solar-induced chlorophyll fluorescence (SIF) dataset that is closely linked to plant photosynthesis. This new dataset has higher spatial and temporal resolutions, and lower uncertainty compared to the existing satellite retrievals. We also demonstrated its application in monitoring drought and improving the understanding of the SIF–photosynthesis relationship.
Alexander Vasilkov, Eun-Su Yang, Sergey Marchenko, Wenhan Qin, Lok Lamsal, Joanna Joiner, Nickolay Krotkov, David Haffner, Pawan K. Bhartia, and Robert Spurr
Atmos. Meas. Tech., 11, 4093–4107, https://doi.org/10.5194/amt-11-4093-2018, https://doi.org/10.5194/amt-11-4093-2018, 2018
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We discuss a new cloud algorithm that retrieves effective cloud fraction and cloud altitude and pressure from the oxygen dimer absorption band at 477 nm. The algorithm accounts for how changes in the sun–satellite geometry affect the surface reflection. The cloud fraction and pressure are used as inputs to the OMI algorithm that retrieves a pollutant gas called nitrogen dioxide. Impacts of the application of the newly developed cloud algorithm on the OMI nitrogen dioxide retrieval are discussed.
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.
Jungbin Mok, Nickolay A. Krotkov, Omar Torres, Hiren Jethva, Zhanqing Li, Jhoon Kim, Ja-Ho Koo, Sujung Go, Hitoshi Irie, Gordon Labow, Thomas F. Eck, Brent N. Holben, Jay Herman, Robert P. Loughman, Elena Spinei, Seoung Soo Lee, Pradeep Khatri, and Monica Campanelli
Atmos. Meas. Tech., 11, 2295–2311, https://doi.org/10.5194/amt-11-2295-2018, https://doi.org/10.5194/amt-11-2295-2018, 2018
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Measuring aerosol absorption from the shortest ultraviolet (UV) to the near-infrared (NIR) wavelengths is important for studies of climate, tropospheric photochemistry, human health, and agricultural productivity. We estimate the accuracy and demonstrate consistency of aerosol absorption retrievals from different instruments, after accounting for spectrally varying surface albedo and gaseous absorption.
Anders V. Lindfors, Jukka Kujanpää, Niilo Kalakoski, Anu Heikkilä, Kaisa Lakkala, Tero Mielonen, Maarten Sneep, Nickolay A. Krotkov, Antti Arola, and Johanna Tamminen
Atmos. Meas. Tech., 11, 997–1008, https://doi.org/10.5194/amt-11-997-2018, https://doi.org/10.5194/amt-11-997-2018, 2018
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This paper describes the algorithm that will be used for estimating surface UV radiation from TROPOMI (TROPOspheric Monitoring Instrument) measurements. TROPOMI is the only payload of the Sentinel-5 Precursor (S5P), which is a polar-orbiting satellite mission of the European Space Agency (ESA). The presented algorithm has been tested using input based on previous satellite measurements. These preliminary results indicate that the algorithm is functioning according to expectations.
Jerald R. Ziemke, Sarah A. Strode, Anne R. Douglass, Joanna Joiner, Alexander Vasilkov, Luke D. Oman, Junhua Liu, Susan E. Strahan, Pawan K. Bhartia, and David P. Haffner
Atmos. Meas. Tech., 10, 4067–4078, https://doi.org/10.5194/amt-10-4067-2017, https://doi.org/10.5194/amt-10-4067-2017, 2017
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We combine satellite measurements of ozone and cloud properties from the Aura OMI and MLS instruments for 2004–2016 to measure ozone in the mid–upper levels of deep convective clouds. Our results ascribe upward injection of low boundary layer ozone (varying from low to high amounts) as a major driver of the measured concentrations of ozone in thick clouds. Our OMI/MLS generated ozone product is made available to the public for use in science applications.
Vitali Fioletov, Chris A. McLinden, Shailesh K. Kharol, Nickolay A. Krotkov, Can Li, Joanna Joiner, Michael D. Moran, Robert Vet, Antoon J. H. Visschedijk, and Hugo A. C. Denier van der Gon
Atmos. Chem. Phys., 17, 12597–12616, https://doi.org/10.5194/acp-17-12597-2017, https://doi.org/10.5194/acp-17-12597-2017, 2017
Nickolay A. Krotkov, Lok N. Lamsal, Edward A. Celarier, William H. Swartz, Sergey V. Marchenko, Eric J. Bucsela, Ka Lok Chan, Mark Wenig, and Marina Zara
Atmos. Meas. Tech., 10, 3133–3149, https://doi.org/10.5194/amt-10-3133-2017, https://doi.org/10.5194/amt-10-3133-2017, 2017
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We describe the new version 3 OMI NO2 standard product (SPv3) based on significant improvements in both the estimation of the SCDs and the AMFs. The new SCDs and stratospheric VCDs are systematically lower (by ~ 10–40 %) than previous estimates. Tropospheric VCDs are also reduced over polluted areas. Initial evaluation over unpolluted areas has shown that the new SPv3 products agree better with independent satellite- and ground-based FTIR measurements.
Georgina M. Miles, Richard Siddans, Roy G. Grainger, Alfred J. Prata, Bradford Fisher, and Nickolay Krotkov
Atmos. Meas. Tech., 10, 2687–2702, https://doi.org/10.5194/amt-10-2687-2017, https://doi.org/10.5194/amt-10-2687-2017, 2017
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Volcanic eruptions are important in the way they perturb the climate and help us understand atmospheric processes. We show a new method to measure the SO2 released by explosive volcanic eruptions using the HIRS/2 satellite instrument, which measured atmospheric temperature and H2O. We apply the technique to the 1991 eruption of Cerro Hudson and show it is possible to detect SO2 with a good degree of accuracy. This method and instrument can potentially generate a climate-significant record.
Hyun-Deok Choi, Hongyu Liu, James H. Crawford, David B. Considine, Dale J. Allen, Bryan N. Duncan, Larry W. Horowitz, Jose M. Rodriguez, Susan E. Strahan, Lin Zhang, Xiong Liu, Megan R. Damon, and Stephen D. Steenrod
Atmos. Chem. Phys., 17, 8429–8452, https://doi.org/10.5194/acp-17-8429-2017, https://doi.org/10.5194/acp-17-8429-2017, 2017
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We evaluate global ozone–carbon monoxide (O3–CO) correlations in a chemistry and transport model during July–August with TES-Aura satellite observations and examine the sensitivity of model simulations to input meteorological data and emissions. Results show that O3–CO correlations may be used effectively to constrain the sources of regional tropospheric O3 in global 3-D models, especially for those regions where convective transport of pollution plays an important role.
Yan Zhang, Can Li, Nickolay A. Krotkov, Joanna Joiner, Vitali Fioletov, and Chris McLinden
Atmos. Meas. Tech., 10, 1495–1509, https://doi.org/10.5194/amt-10-1495-2017, https://doi.org/10.5194/amt-10-1495-2017, 2017
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In this study, we demonstrate a very good consistency of the SO2 retrievals from OMI and OMPS using our state-of-the-art principal component analysis technique. Four full years of OMI and OMPS SO2 retrievals, during 2012–2015 have been analyzed over some of the world’s most polluted regions: eastern China, Mexico, and South Africa. The consistency of retrievals between OMI and OMPS make it possible to continue the long-term global SO2 pollution monitoring.
Alba Lorente, K. Folkert Boersma, Huan Yu, Steffen Dörner, Andreas Hilboll, Andreas Richter, Mengyao Liu, Lok N. Lamsal, Michael Barkley, Isabelle De Smedt, Michel Van Roozendael, Yang Wang, Thomas Wagner, Steffen Beirle, Jin-Tai Lin, Nickolay Krotkov, Piet Stammes, Ping Wang, Henk J. Eskes, and Maarten Krol
Atmos. Meas. Tech., 10, 759–782, https://doi.org/10.5194/amt-10-759-2017, https://doi.org/10.5194/amt-10-759-2017, 2017
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Choices and assumptions made to represent the state of the atmosphere introduce an uncertainty of 42 % in the air mass factor calculation in trace gas satellite retrievals in polluted regions. The AMF strongly depends on the choice of a priori trace gas profile, surface albedo data set and the correction method to account for clouds and aerosols. We call for well-designed validation exercises focusing on situations when AMF structural uncertainty has the highest impact on satellite retrievals.
Can Li, Nickolay A. Krotkov, Simon Carn, Yan Zhang, Robert J. D. Spurr, and Joanna Joiner
Atmos. Meas. Tech., 10, 445–458, https://doi.org/10.5194/amt-10-445-2017, https://doi.org/10.5194/amt-10-445-2017, 2017
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In this paper, we describe the new-generation OMI volcanic SO2 algorithm based on our principal component analysis (PCA) retrieval technique. We demonstrate significant improvement in the our new OMI volcanic SO2 data, with the retrieval noise reduced by a factor of 2 as compared with the previous dataset. The algorithm also improves the accuracy for large volcanic eruptions. It is also capable of producing consistent retrievals between different instruments.
Alexander Vasilkov, Wenhan Qin, Nickolay Krotkov, Lok Lamsal, Robert Spurr, David Haffner, Joanna Joiner, Eun-Su Yang, and Sergey Marchenko
Atmos. Meas. Tech., 10, 333–349, https://doi.org/10.5194/amt-10-333-2017, https://doi.org/10.5194/amt-10-333-2017, 2017
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We show how the surface reflection can vary day to day in the blue part of the sun's spectrum where we measure the pollutant gas nitrogen dioxide using a satellite instrument called OMI. We use information from an imaging spectrometer on another satellite, MODIS, to estimate the angular surface effects. We can then use models of how the sunlight travels through the atmosphere to predict how the angle-dependent surface reflection will impact the values of pollutant levels inferred by OMI.
Iolanda Ialongo, Jay Herman, Nick Krotkov, Lok Lamsal, K. Folkert Boersma, Jari Hovila, and Johanna Tamminen
Atmos. Meas. Tech., 9, 5203–5212, https://doi.org/10.5194/amt-9-5203-2016, https://doi.org/10.5194/amt-9-5203-2016, 2016
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We present the comparison between satellite- and ground-based atmospheric NO2 observations in Helsinki (Finland). The results show that, despite some limitations due to cloud contamination and low solar angles, satellite data are able to describe urban air quality features such as the weekly and seasonal cycles. The results support air quality satellite data exploitation at high latitudes and prepare for similar applications for future missions.
Wonbae Jeon, Yunsoo Choi, Peter Percell, Amir Hossein Souri, Chang-Keun Song, Soon-Tae Kim, and Jhoon Kim
Geosci. Model Dev., 9, 3671–3684, https://doi.org/10.5194/gmd-9-3671-2016, https://doi.org/10.5194/gmd-9-3671-2016, 2016
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This study suggests a new hybrid Lagrangian–Eulerian modeling tool (the Screening Trajectory Ozone Prediction System, STOPS) for an accurate/fast prediction of Asian dust events. The STOPS is a moving nest (Lagrangian approach) between the source and the receptor inside Eulerian model. We run STOPS, instead of running a time-consuming Eulerian model, using constrained PM concentration from remote sensing aerosol optical depth, reflecting real-time dust particles. STOPS is for unexpected events.
Vitali E. Fioletov, Chris A. McLinden, Nickolay Krotkov, Can Li, Joanna Joiner, Nicolas Theys, Simon Carn, and Mike D. Moran
Atmos. Chem. Phys., 16, 11497–11519, https://doi.org/10.5194/acp-16-11497-2016, https://doi.org/10.5194/acp-16-11497-2016, 2016
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We introduce the first space-based catalogue of SO2 emission sources seen by OMI. The inventory contains about 500 sources. They account for about a half of all SO2 emissions; the remaining half is likely related to sources emitting less than 30 kt yr−1 and not detected by OMI. The sources are grouped by type (volcanoes, power plants, oil- and gas-related sources, and smelters) and country. The catalogue presented herein can be used for verification of available SO2 emission inventories.
Cristen Adams, Elise N. Normand, Chris A. McLinden, Adam E. Bourassa, Nicholas D. Lloyd, Douglas A. Degenstein, Nickolay A. Krotkov, Maria Belmonte Rivas, K. Folkert Boersma, and Henk Eskes
Atmos. Meas. Tech., 9, 4103–4122, https://doi.org/10.5194/amt-9-4103-2016, https://doi.org/10.5194/amt-9-4103-2016, 2016
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A new "OMI-minus-OSIRIS" (OmO) prototype dataset for tropospheric NO2 was created by combining information from the OMI satellite instrument, which is sensitive to NO2 in both the troposphere and stratosphere, with information from the OSIRIS satellite instrument, which measures NO2 in the stratosphere. This paper demonstrates that this approach is feasible and could be applied to future geostationary missions.
Joanna Joiner, Yasuko Yoshida, Luis Guanter, and Elizabeth M. Middleton
Atmos. Meas. Tech., 9, 3939–3967, https://doi.org/10.5194/amt-9-3939-2016, https://doi.org/10.5194/amt-9-3939-2016, 2016
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We examine new ways to use existing satellite instruments to retrieve red solar-induced fluorescence (SIF) over land and ocean. Our 8-year record of red SIF observations over land with the Global Ozone Monitoring Instrument 2 (GOME-2) shows for the first time reductions in response to drought. High-quality ocean fluorescence can also be derived with GOME-2 and similar instruments by utilizing their rich measurements of different colors.
Gonzalo González Abad, Alexander Vasilkov, Colin Seftor, Xiong Liu, and Kelly Chance
Atmos. Meas. Tech., 9, 2797–2812, https://doi.org/10.5194/amt-9-2797-2016, https://doi.org/10.5194/amt-9-2797-2016, 2016
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The multi-spectral possibilities of the OMPS Nadir Mapper instrument are exploited here to perform formaldehyde retrievals. Orbiting the Earth at 824 km, OMPS observes the atmosphere in a time frame similar to instruments belonging to NASA's A-Train constellation, 01:30. We show that OMPS is well suited to measure formaldehyde despite its spectral resolution of 1nm. The comparison of OMPS retrievals with OMI products show good temporal correlation.
Pawan Gupta, Joanna Joiner, Alexander Vasilkov, and Pawan K. Bhartia
Atmos. Meas. Tech., 9, 2813–2826, https://doi.org/10.5194/amt-9-2813-2016, https://doi.org/10.5194/amt-9-2813-2016, 2016
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The A-train constellation of satellites provides a unique opportunity to analyze near-simultaneous data from several of these sensors. In this paper, retrievals of cloud/aerosols parameters and total column ozone (TCO) from the Aura Ozone Monitoring Instrument (OMI) have been used to develop a variety of neural networks that estimate TOA SWF globally over ocean and land using only OMI data as inputs. Application of our method to other ultraviolet sensors may provide unique estimates of TOA SWF.
Sarah A. Strode, Helen M. Worden, Megan Damon, Anne R. Douglass, Bryan N. Duncan, Louisa K. Emmons, Jean-Francois Lamarque, Michael Manyin, Luke D. Oman, Jose M. Rodriguez, Susan E. Strahan, and Simone Tilmes
Atmos. Chem. Phys., 16, 7285–7294, https://doi.org/10.5194/acp-16-7285-2016, https://doi.org/10.5194/acp-16-7285-2016, 2016
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We use global models to interpret trends in MOPITT observations of CO. Simulations with time-dependent emissions reproduce the observed trends over the eastern USA and Europe, suggesting that the emissions are reasonable for these regions. The simulations produce a positive trend over eastern China, contrary to the observed negative trend. This may indicate that the assumed emission trend over China is too positive. However, large variability in the overhead ozone column also contributes.
Nickolay A. Krotkov, Chris A. McLinden, Can Li, Lok N. Lamsal, Edward A. Celarier, Sergey V. Marchenko, William H. Swartz, Eric J. Bucsela, Joanna Joiner, Bryan N. Duncan, K. Folkert Boersma, J. Pepijn Veefkind, Pieternel F. Levelt, Vitali E. Fioletov, Russell R. Dickerson, Hao He, Zifeng Lu, and David G. Streets
Atmos. Chem. Phys., 16, 4605–4629, https://doi.org/10.5194/acp-16-4605-2016, https://doi.org/10.5194/acp-16-4605-2016, 2016
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We examine changes in SO2 and NO2 over the world's most polluted regions during the first decade of Aura OMI observations. Over the eastern US, both NO2 and SO2 levels decreased by 40 % and 80 %, respectively. OMI confirmed large reductions in SO2 over eastern Europe's largest coal power plants. The North China Plain has the world's most severe SO2 pollution, but a decreasing trend been observed since 2011, with a 50 % reduction in 2012–2014. India's SO2 and NO2 levels are growing at a fast pace.
Yasin F. Elshorbany, Bryan N. Duncan, Sarah A. Strode, James S. Wang, and Jules Kouatchou
Geosci. Model Dev., 9, 799–822, https://doi.org/10.5194/gmd-9-799-2016, https://doi.org/10.5194/gmd-9-799-2016, 2016
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The ECCOH (pronounced "echo") chemistry module interactively simulates the photochemistry of the CH4–CO–OH system within a chemistry climate model, carbon cycle model, or Earth system model. The computational efficiency of the module allows many multi-decadal sensitivity simulations of the CH4–CO–OH system. This capability is important for capturing nonlinear feedbacks of the CH4–CO–OH system and understanding the perturbations to methane, CO, and OH and the concomitant climate impacts.
S. A. Strode, B. N. Duncan, E. A. Yegorova, J. Kouatchou, J. R. Ziemke, and A. R. Douglass
Atmos. Chem. Phys., 15, 11789–11805, https://doi.org/10.5194/acp-15-11789-2015, https://doi.org/10.5194/acp-15-11789-2015, 2015
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A low bias in carbon monoxide (CO) at northern latitudes is a common feature of chemistry climate models. We find that increasing Northern Hemisphere (NH) CO emissions or reducing NH OH concentrations improves the agreement with CO surface observations, but reducing NH OH leads to a better comparison with MOPITT. Removing model biases in ozone and water vapor increases the simulated methane lifetime, but it does not give the 20% reduction in NH OH suggested by our analysis of the CO bias.
Z. Lu, D. G. Streets, B. de Foy, L. N. Lamsal, B. N. Duncan, and J. Xing
Atmos. Chem. Phys., 15, 10367–10383, https://doi.org/10.5194/acp-15-10367-2015, https://doi.org/10.5194/acp-15-10367-2015, 2015
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Using an exponentially modified Gaussian method and taking into account the effect of wind on NO2 distributions, we estimate 3-year moving-average emissions of summertime NOx from 35 US urban areas directly from NO2 retrievals of the OMI during 2005−2014. Total OMI-derived NOx emissions over US urban areas decreased by 49%, consistent with reductions of 43, 49, and 44% in the bottom-up NOx emissions, the weak-wind OMI NO2 burdens, and the averaged NO2 concentrations, respectively.
P. Köhler, L. Guanter, and J. Joiner
Atmos. Meas. Tech., 8, 2589–2608, https://doi.org/10.5194/amt-8-2589-2015, https://doi.org/10.5194/amt-8-2589-2015, 2015
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The paper presents recent developments for the retrieval of sun-induced fluorescence (SIF) from medium spectral resolution space-borne spectrometers such as the Global Ozone Monitoring Experiment (GOME-2) and the Scanning Imaging Absorption SpectroMeter for Atmospheric ChartographY (SCIAMACHY). Beside using simulated radiances to evaluate the retrieval performance, the method has also been used to estimate SIF at 740 nm using real spectra from GOME-2 and for the first time, from SCIAMACHY.
L. K. Emmons, S. R. Arnold, S. A. Monks, V. Huijnen, S. Tilmes, K. S. Law, J. L. Thomas, J.-C. Raut, I. Bouarar, S. Turquety, Y. Long, B. Duncan, S. Steenrod, S. Strode, J. Flemming, J. Mao, J. Langner, A. M. Thompson, D. Tarasick, E. C. Apel, D. R. Blake, R. C. Cohen, J. Dibb, G. S. Diskin, A. Fried, S. R. Hall, L. G. Huey, A. J. Weinheimer, A. Wisthaler, T. Mikoviny, J. Nowak, J. Peischl, J. M. Roberts, T. Ryerson, C. Warneke, and D. Helmig
Atmos. Chem. Phys., 15, 6721–6744, https://doi.org/10.5194/acp-15-6721-2015, https://doi.org/10.5194/acp-15-6721-2015, 2015
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Eleven 3-D tropospheric chemistry models have been compared and evaluated with observations in the Arctic during the International Polar Year (IPY 2008). Large differences are seen among the models, particularly related to the model chemistry of volatile organic compounds (VOCs) and reactive nitrogen (NOx, PAN, HNO3) partitioning. Consistency among the models in the underestimation of CO, ethane and propane indicates the emission inventory is too low for these compounds.
S. R. Arnold, L. K. Emmons, S. A. Monks, K. S. Law, D. A. Ridley, S. Turquety, S. Tilmes, J. L. Thomas, I. Bouarar, J. Flemming, V. Huijnen, J. Mao, B. N. Duncan, S. Steenrod, Y. Yoshida, J. Langner, and Y. Long
Atmos. Chem. Phys., 15, 6047–6068, https://doi.org/10.5194/acp-15-6047-2015, https://doi.org/10.5194/acp-15-6047-2015, 2015
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The extent to which forest fires produce the air pollutant and greenhouse gas ozone (O3) in the atmosphere at high latitudes in not well understood. We have compared how fire emissions produce O3 and its precursors in several models of atmospheric chemistry. We find enhancements in O3 in air dominated by fires in all models, which increase on average as fire emissions age. We also find that in situ O3 production in the Arctic is sensitive to details of organic chemistry and vertical lifting.
I. Ialongo, J. Hakkarainen, R. Kivi, P. Anttila, N. A. Krotkov, K. Yang, C. Li, S. Tukiainen, S. Hassinen, and J. Tamminen
Atmos. Meas. Tech., 8, 2279–2289, https://doi.org/10.5194/amt-8-2279-2015, https://doi.org/10.5194/amt-8-2279-2015, 2015
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The SO2 observations from OMI and OMPS satellite instruments are compared to ground-based measurements during the Icelandic Holuhraun fissure eruption in September 2014. The best agreement with the Brewer observations in Sodankylä, Finland can be found, assuming the SO2 predominantly located in the lowest levels of the atmosphere. The analysis of the SO2 surface concentrations in northern Finland supports the hypothesis that the volcanic plume was located very close to the surface.
S. A. Monks, S. R. Arnold, L. K. Emmons, K. S. Law, S. Turquety, B. N. Duncan, J. Flemming, V. Huijnen, S. Tilmes, J. Langner, J. Mao, Y. Long, J. L. Thomas, S. D. Steenrod, J. C. Raut, C. Wilson, M. P. Chipperfield, G. S. Diskin, A. Weinheimer, H. Schlager, and G. Ancellet
Atmos. Chem. Phys., 15, 3575–3603, https://doi.org/10.5194/acp-15-3575-2015, https://doi.org/10.5194/acp-15-3575-2015, 2015
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Multi-model simulations of Arctic CO, O3 and OH are evaluated using observations. Models show highly variable concentrations but the relative importance of emission regions and types is robust across the models, demonstrating the importance of biomass burning as a source. Idealised tracer experiments suggest that some of the model spread is due to variations in simulated transport from Europe in winter and from Asia throughout the year.
L. Guanter, I. Aben, P. Tol, J. M. Krijger, A. Hollstein, P. Köhler, A. Damm, J. Joiner, C. Frankenberg, and J. Landgraf
Atmos. Meas. Tech., 8, 1337–1352, https://doi.org/10.5194/amt-8-1337-2015, https://doi.org/10.5194/amt-8-1337-2015, 2015
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This paper investigates the potential of the upcoming TROPOspheric Monitoring Instrument (TROPOMI) instrument for the retrieval of the chlorophyll fluorescence signal emitted in the 650–850nm spectral range by the photosynthetic machinery of green plants. We find that TROPOMI will allow substantial improvements in the space monitoring of fluorescence with respect to current spaceborne instruments such as GOME-2 and SCIAMACHY.
L. N. Lamsal, N. A. Krotkov, E. A. Celarier, W. H. Swartz, K. E. Pickering, E. J. Bucsela, J. F. Gleason, R. V. Martin, S. Philip, H. Irie, A. Cede, J. Herman, A. Weinheimer, J. J. Szykman, and T. N. Knepp
Atmos. Chem. Phys., 14, 11587–11609, https://doi.org/10.5194/acp-14-11587-2014, https://doi.org/10.5194/acp-14-11587-2014, 2014
A. Rocha-Lima, J. V. Martins, L. A. Remer, N. A. Krotkov, M. H. Tabacniks, Y. Ben-Ami, and P. Artaxo
Atmos. Chem. Phys., 14, 10649–10661, https://doi.org/10.5194/acp-14-10649-2014, https://doi.org/10.5194/acp-14-10649-2014, 2014
A. Vasilkov, J. Joiner, and C. Seftor
Atmos. Meas. Tech., 7, 2897–2906, https://doi.org/10.5194/amt-7-2897-2014, https://doi.org/10.5194/amt-7-2897-2014, 2014
I. Ialongo, J. Hakkarainen, N. Hyttinen, J.-P. Jalkanen, L. Johansson, K. F. Boersma, N. Krotkov, and J. Tamminen
Atmos. Chem. Phys., 14, 7795–7805, https://doi.org/10.5194/acp-14-7795-2014, https://doi.org/10.5194/acp-14-7795-2014, 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
V. Buchard, A. M. da Silva, P. Colarco, N. Krotkov, R. R. Dickerson, J. W. Stehr, G. Mount, E. Spinei, H. L. Arkinson, and H. He
Atmos. Chem. Phys., 14, 1929–1941, https://doi.org/10.5194/acp-14-1929-2014, https://doi.org/10.5194/acp-14-1929-2014, 2014
Y. Choi
Atmos. Chem. Phys., 14, 675–690, https://doi.org/10.5194/acp-14-675-2014, https://doi.org/10.5194/acp-14-675-2014, 2014
J. X. Warner, R. Yang, Z. Wei, F. Carminati, A. Tangborn, Z. Sun, W. Lahoz, J.-L. Attié, L. El Amraoui, and B. Duncan
Atmos. Chem. Phys., 14, 103–114, https://doi.org/10.5194/acp-14-103-2014, https://doi.org/10.5194/acp-14-103-2014, 2014
J. Joiner, L. Guanter, R. Lindstrot, M. Voigt, A. P. Vasilkov, E. M. Middleton, K. F. Huemmrich, Y. Yoshida, and C. Frankenberg
Atmos. Meas. Tech., 6, 2803–2823, https://doi.org/10.5194/amt-6-2803-2013, https://doi.org/10.5194/amt-6-2803-2013, 2013
E. J. Bucsela, N. A. Krotkov, E. A. Celarier, L. N. Lamsal, W. H. Swartz, P. K. Bhartia, K. F. Boersma, J. P. Veefkind, J. F. Gleason, and K. E. Pickering
Atmos. Meas. Tech., 6, 2607–2626, https://doi.org/10.5194/amt-6-2607-2013, https://doi.org/10.5194/amt-6-2607-2013, 2013
A. Vasilkov, J. Joiner, and R. Spurr
Atmos. Meas. Tech., 6, 981–990, https://doi.org/10.5194/amt-6-981-2013, https://doi.org/10.5194/amt-6-981-2013, 2013
J. Wang, S. Park, J. Zeng, C. Ge, K. Yang, S. Carn, N. Krotkov, and A. H. Omar
Atmos. Chem. Phys., 13, 1895–1912, https://doi.org/10.5194/acp-13-1895-2013, https://doi.org/10.5194/acp-13-1895-2013, 2013
Related subject area
Subject: Gases | Research Activity: Remote Sensing | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Biomass burning combustion efficiency observed from space using measurements of CO and NO2 by the TROPOspheric Monitoring Instrument (TROPOMI)
Long-term MAX-DOAS measurements of NO2, HCHO, and aerosols and evaluation of corresponding satellite data products over Mohali in the Indo-Gangetic Plain
Detection and attribution of wildfire pollution in the Arctic and northern midlatitudes using a network of Fourier-transform infrared spectrometers and GEOS-Chem
Validation of satellite formaldehyde (HCHO) retrievals using observations from 12 aircraft campaigns
Long-term time series of Arctic tropospheric BrO derived from UV–VIS satellite remote sensing and its relation to first-year sea ice
2010–2015 North American methane emissions, sectoral contributions, and trends: a high-resolution inversion of GOSAT satellite observations of atmospheric methane
Quantifying burning efficiency in megacities using the NO2∕CO ratio from the Tropospheric Monitoring Instrument (TROPOMI)
Remote sensing of methane leakage from natural gas and petroleum systems revisited
Validation of Aura-OMI QA4ECV NO2 climate data records with ground-based DOAS networks: the role of measurement and comparison uncertainties
Effects of a priori profile shape assumptions on comparisons between satellite NO2 columns and model simulations
Anthropogenic and volcanic point source SO2 emissions derived from TROPOMI on board Sentinel-5 Precursor: first results
Severe Californian wildfires in November 2018 observed from space: the carbon monoxide perspective
Ammonia measurements from space with the Cross-track Infrared Sounder: characteristics and applications
Unexpected long-range transport of glyoxal and formaldehyde observed from the Copernicus Sentinel-5 Precursor satellite during the 2018 Canadian wildfires
Atmospheric ammonia variability and link with particulate matter formation: a case study over the Paris area
The impact of improved satellite retrievals on estimates of biospheric carbon balance
A methodology to constrain carbon dioxide emissions from coal-fired power plants using satellite observations of co-emitted nitrogen dioxide
Inferring the anthropogenic NOx emission trend over the United States during 2003–2017 from satellite observations: was there a flattening of the emission trend after the Great Recession?
Surveillance of SO2 and NO2 from ship emissions by MAX-DOAS measurements and the implications regarding fuel sulfur content compliance
New constraints on biogenic emissions using satellite-based estimates of carbon monoxide fluxes
Lightning NO2 simulation over the contiguous US and its effects on satellite NO2 retrievals
Detection of outflow of formaldehyde and glyoxal from the African continent to the Atlantic Ocean with a MAX-DOAS instrument
Deriving tropospheric ozone from assimilated profiles
Primary and secondary sources of ambient formaldehyde in the Yangtze River Delta based on Ozone Mapping and Profiler Suite (OMPS) observations
An evaluation of the ability of the Ozone Monitoring Instrument (OMI) to observe boundary layer ozone pollution across China: application to 2005–2017 ozone trends
Near-surface and path-averaged mixing ratios of NO2 derived from car DOAS zenith-sky and tower DOAS off-axis measurements in Vienna: a case study
Vertical profiles of NO2, SO2, HONO, HCHO, CHOCHO and aerosols derived from MAX-DOAS measurements at a rural site in the central western North China Plain and their relation to emission sources and effects of regional transport
Satellite data reveal a common combustion emission pathway for major cities in China
What caused the extreme CO concentrations during the 2017 high-pollution episode in India?
Satellite-derived emissions of carbon monoxide, ammonia, and nitrogen dioxide from the 2016 Horse River wildfire in the Fort McMurray area
A top-down assessment using OMI NO2 suggests an underestimate in the NOx emissions inventory in Seoul, South Korea, during KORUS-AQ
Computation and analysis of atmospheric carbon dioxide annual mean growth rates from satellite observations during 2003–2016
A new global anthropogenic SO2 emission inventory for the last decade: a mosaic of satellite-derived and bottom-up emissions
Lower tropospheric ozone over the North China Plain: variability and trends revealed by IASI satellite observations for 2008–2016
Southern California megacity CO2, CH4, and CO flux estimates using ground- and space-based remote sensing and a Lagrangian model
Monitoring global tropospheric OH concentrations using satellite observations of atmospheric methane
Tropospheric NO2, SO2, and HCHO over the East China Sea, using ship-based MAX-DOAS observations and comparison with OMI and OMPS satellite data
Adjoint inversion of Chinese non-methane volatile organic compound emissions using space-based observations of formaldehyde and glyoxal
Characterization of trace gas emissions at an intermediate port
Transboundary ozone pollution across East Asia: daily evolution and photochemical production analysed by IASI + GOME2 multispectral satellite observations and models
Influence of the wintertime North Atlantic Oscillation on European tropospheric composition: an observational and modelling study
Impact of high-resolution a priori profiles on satellite-based formaldehyde retrievals
Decrease in tropospheric O3 levels in the Northern Hemisphere observed by IASI
The Ozone Monitoring Instrument: overview of 14 years in space
Using TES retrievals to investigate PAN in North American biomass burning plumes
Which processes drive observed variations of HCHO columns over India?
Characterizing sampling and quality screening biases in infrared and microwave limb sounding
Simultaneous assimilation of ozone profiles from multiple UV-VIS satellite instruments
Atmospheric pollution over the eastern Mediterranean during summer – a review
Multi-source SO2 emission retrievals and consistency of satellite and surface measurements with reported emissions
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.
Vinod Kumar, Steffen Beirle, Steffen Dörner, Abhishek Kumar Mishra, Sebastian Donner, Yang Wang, Vinayak Sinha, and Thomas Wagner
Atmos. Chem. Phys., 20, 14183–14235, https://doi.org/10.5194/acp-20-14183-2020, https://doi.org/10.5194/acp-20-14183-2020, 2020
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We present the first long-term MAX-DOAS measurements of aerosols, nitrogen dioxide and formaldehyde tropospheric columns, vertical distributions, and temporal variation from Mohali in the Indo-Gangetic Plain. We investigate the effect of various emission sources and meteorological conditions on the measured pollutants and how they control ozone formation. These measurements are also used to validate the corresponding satellite observations and are also compared against in situ observations.
Erik Lutsch, Kimberly Strong, Dylan B. A. Jones, Thomas Blumenstock, Stephanie Conway, Jenny A. Fisher, James W. Hannigan, Frank Hase, Yasuko Kasai, Emmanuel Mahieu, Maria Makarova, Isamu Morino, Tomoo Nagahama, Justus Notholt, Ivan Ortega, Mathias Palm, Anatoly V. Poberovskii, Ralf Sussmann, and Thorsten Warneke
Atmos. Chem. Phys., 20, 12813–12851, https://doi.org/10.5194/acp-20-12813-2020, https://doi.org/10.5194/acp-20-12813-2020, 2020
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This paper describes the use of a network of 10 Arctic and midlatitude ground-based FTIR measurement sites to detect enhancements of the wildfire tracers carbon monoxide, hydrogen cyanide, and ethane from 2003 to 2018. A tagged CO GEOS-Chem simulation is used for source attribution and to evaluate the relative contribution of CO sources to the FTIR measurements. The use of FTIR measurements allowed for the emission ratios of hydrogen cyanide and ethane to be quantified.
Lei Zhu, Gonzalo González Abad, Caroline R. Nowlan, Christopher Chan Miller, Kelly Chance, Eric C. Apel, Joshua P. DiGangi, Alan Fried, Thomas F. Hanisco, Rebecca S. Hornbrook, Lu Hu, Jennifer Kaiser, Frank N. Keutsch, Wade Permar, Jason M. St. Clair, and Glenn M. Wolfe
Atmos. Chem. Phys., 20, 12329–12345, https://doi.org/10.5194/acp-20-12329-2020, https://doi.org/10.5194/acp-20-12329-2020, 2020
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We develop a validation platform for satellite HCHO retrievals using in situ observations from 12 aircraft campaigns. The platform offers an alternative way to quickly assess systematic biases in HCHO satellite products over large domains and long periods, facilitating optimization of retrieval settings and the minimization of retrieval biases. Application to the NASA operational HCHO product indicates that relative biases range from −44.5 % to +112.1 % depending on locations and seasons.
Ilias Bougoudis, Anne-Marlene Blechschmidt, Andreas Richter, Sora Seo, John Philip Burrows, Nicolas Theys, and Annette Rinke
Atmos. Chem. Phys., 20, 11869–11892, https://doi.org/10.5194/acp-20-11869-2020, https://doi.org/10.5194/acp-20-11869-2020, 2020
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A 22-year (1996 to 2017) consistent Arctic tropospheric BrO dataset derived from four satellite remote sensing instruments is presented. An increase in tropospheric BrO VCDs over this period, and especially during polar springs, can be seen. Comparisons of tropospheric BrO VCDs with first-year sea ice reveal a moderate spatial and temporal correlation between the two, suggesting that the increase in first-year sea ice in the Arctic has an impact on tropospheric BrO abundancies.
Joannes D. Maasakkers, Daniel J. Jacob, Melissa P. Sulprizio, Tia R. Scarpelli, Hannah Nesser, Jianxiong Sheng, Yuzhong Zhang, Xiao Lu, A. Anthony Bloom, Kevin W. Bowman, John R. Worden, and Robert J. Parker
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2020-915, https://doi.org/10.5194/acp-2020-915, 2020
Revised manuscript accepted for ACP
Srijana Lama, Sander Houweling, K. Folkert Boersma, Henk Eskes, Ilse Aben, Hugo A. C. Denier van der Gon, Maarten C. Krol, Han Dolman, Tobias Borsdorff, and Alba Lorente
Atmos. Chem. Phys., 20, 10295–10310, https://doi.org/10.5194/acp-20-10295-2020, https://doi.org/10.5194/acp-20-10295-2020, 2020
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Rapid urbanization has increased the consumption of fossil fuel, contributing the degradation of urban air quality. Burning efficiency is a major factor determining the impact of fuel burning on the environment. We quantify the burning efficiency of fossil fuel use over six megacities using satellite remote sensing data. City governance can use these results to understand air pollution scenarios and to formulate effective air pollution control strategies.
Oliver Schneising, Michael Buchwitz, Maximilian Reuter, Steffen Vanselow, Heinrich Bovensmann, and John P. Burrows
Atmos. Chem. Phys., 20, 9169–9182, https://doi.org/10.5194/acp-20-9169-2020, https://doi.org/10.5194/acp-20-9169-2020, 2020
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The switch from the use of coal to natural gas or oil for energy generation potentially reduces the impact on global warming due to lower CO2 emissions with the same energy content. However, this climate benefit is offset by fugitive methane emissions during the production and distribution process. We quantify emission and leakage rates relative to production for several large production regions based on satellite observations to evaluate the climate footprint of the gas and oil industry.
Steven Compernolle, Tijl Verhoelst, Gaia Pinardi, José Granville, Daan Hubert, Arno Keppens, Sander Niemeijer, Bruno Rino, Alkis Bais, Steffen Beirle, Folkert Boersma, John P. Burrows, Isabelle De Smedt, Henk Eskes, Florence Goutail, François Hendrick, Alba Lorente, Andrea Pazmino, Ankie Piters, Enno Peters, Jean-Pierre Pommereau, Julia Remmers, Andreas Richter, Jos van Geffen, Michel Van Roozendael, Thomas Wagner, and Jean-Christopher Lambert
Atmos. Chem. Phys., 20, 8017–8045, https://doi.org/10.5194/acp-20-8017-2020, https://doi.org/10.5194/acp-20-8017-2020, 2020
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Tropospheric and stratospheric NO2 columns from the OMI QA4ECV NO2 satellite product are validated by comparison with ground-based measurements at 11 sites. The OMI stratospheric column has a small negative bias, and the OMI tropospheric column has a stronger negative bias relative to the ground-based data. Discrepancies are attributed to comparison errors (e.g. difference in horizontal smoothing) and measurement errors (e.g. clouds, aerosols, vertical smoothing and a priori profile assumptions).
Matthew J. Cooper, Randall V. Martin, Daven K. Henze, and Dylan B. A. Jones
Atmos. Chem. Phys., 20, 7231–7241, https://doi.org/10.5194/acp-20-7231-2020, https://doi.org/10.5194/acp-20-7231-2020, 2020
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Comparisons between satellite-retrieved and model-simulated NO2 columns are affected by differences between the model vertical profile and the assumed profile used in the retrieval process. We examine how such differences impact NOx emission estimates from satellite observations. Larger differences between the simulated and assumed profile shape correspond to larger emission errors. This reveals the importance of using consistent profile information when comparing satellite columns to models.
Vitali Fioletov, Chris A. McLinden, Debora Griffin, Nicolas Theys, Diego G. Loyola, Pascal Hedelt, Nickolay A. Krotkov, and Can Li
Atmos. Chem. Phys., 20, 5591–5607, https://doi.org/10.5194/acp-20-5591-2020, https://doi.org/10.5194/acp-20-5591-2020, 2020
Oliver Schneising, Michael Buchwitz, Maximilian Reuter, Heinrich Bovensmann, and John P. Burrows
Atmos. Chem. Phys., 20, 3317–3332, https://doi.org/10.5194/acp-20-3317-2020, https://doi.org/10.5194/acp-20-3317-2020, 2020
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As a consequence of climate change, droughts in California are occurring more often, providing ample fuel for destructive wildfires. The associated smoke is reducing air quality as it contains pollutants considered harmful to public health and the environment such as carbon monoxide (CO). We analyse the statewide distribution of CO during the first days of two specific wildfires using satellite measurements and assess the corresponding air quality burden in major Californian cities.
Mark W. Shephard, Enrico Dammers, Karen E. Cady-Pereira, Shailesh K. Kharol, Jesse Thompson, Yonatan Gainariu-Matz, Junhua Zhang, Chris A. McLinden, Andrew Kovachik, Michael Moran, Shabtai Bittman, Christopher E. Sioris, Debora Griffin, Matthew J. Alvarado, Chantelle Lonsdale, Verica Savic-Jovcic, and Qiong Zheng
Atmos. Chem. Phys., 20, 2277–2302, https://doi.org/10.5194/acp-20-2277-2020, https://doi.org/10.5194/acp-20-2277-2020, 2020
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Presented is a description and survey demonstrating the capabilities of the CrIS ammonia product for monitoring, air quality forecast model evaluation, dry deposition estimates, and emission estimates of an agricultural hotspot.
Leonardo M. A. Alvarado, Andreas Richter, Mihalis Vrekoussis, Andreas Hilboll, Anna B. Kalisz Hedegaard, Oliver Schneising, and John P. Burrows
Atmos. Chem. Phys., 20, 2057–2072, https://doi.org/10.5194/acp-20-2057-2020, https://doi.org/10.5194/acp-20-2057-2020, 2020
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We present CHOCHO and HCHO columns retrieved from measurements by TROPOMI. Elevated amounts of CHOCHO and HCHO are observed during the fire season in BC, Canada, where a large number of fires occurred in 2018. CHOCHO and HCHO plumes from individual fires are observed in air masses travelling over distances of up to 1500 km. Comparison with FLEXPART simulations with different lifetimes shows that effective lifetimes of 20 h and more are needed to explain the observations.
Camille Viatte, Tianze Wang, Martin Van Damme, Enrico Dammers, Frederik Meleux, Lieven Clarisse, Mark W. Shephard, Simon Whitburn, Pierre François Coheur, Karen E. Cady-Pereira, and Cathy Clerbaux
Atmos. Chem. Phys., 20, 577–596, https://doi.org/10.5194/acp-20-577-2020, https://doi.org/10.5194/acp-20-577-2020, 2020
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We study concentrations and spatiotemporal variabilities of atmospheric NH3 from the agricultural sector to gain insights on its effects on the Paris megacity air quality using satellite data from IASI and CrIS.
We evaluate the regional CHIMERE model capacity to reproduce NH3 and particulate matter (PM2.5) concentrations and variabilities in the domain of study.
We quantify the main meteorological parameters driving the optimal conditions involved in the PM2.5 formation from NH3 in Paris.
Scot M. Miller and Anna M. Michalak
Atmos. Chem. Phys., 20, 323–331, https://doi.org/10.5194/acp-20-323-2020, https://doi.org/10.5194/acp-20-323-2020, 2020
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NASA's Orbiting Carbon Observatory 2 (OCO-2) satellite observes CO2 in the atmosphere. The satellite measures radiation, and these measurements are then converted to an estimate of atmospheric CO2. This conversion or retrieval algorithm has improved markedly since the satellite launch. We find that these improvements in the CO2 retrieval are having a potentially transformative effect on satellite-based estimates of the global biospheric carbon balance.
Fei Liu, Bryan N. Duncan, Nickolay A. Krotkov, Lok N. Lamsal, Steffen Beirle, Debora Griffin, Chris A. McLinden, Daniel L. Goldberg, and Zifeng Lu
Atmos. Chem. Phys., 20, 99–116, https://doi.org/10.5194/acp-20-99-2020, https://doi.org/10.5194/acp-20-99-2020, 2020
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We present a novel method to infer CO2 emissions from individual power plants, based on satellite observations of co-emitted NO2. We find that the CO2 emissions estimated by our satellite-based method during 2005–2017 are in reasonable agreement with the CEMS measurements for US power plants. The broader implication of our methodology is that it has the potential to provide an additional constraint on CO2 emissions from power plants in regions of the world without reliable emissions accounting.
Jianfeng Li and Yuhang Wang
Atmos. Chem. Phys., 19, 15339–15352, https://doi.org/10.5194/acp-19-15339-2019, https://doi.org/10.5194/acp-19-15339-2019, 2019
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NO2 tropospheric vertical columns (TVCDs) and surface concentrations are widely used proxies for NOx emission variations. Through model and observation analyses, we find that satellite NO2 TVCDs provide much better information on anthropogenic NOx emission variations over urban than rural regions. NO2 surface observations, satellite column datasets, and EPA anthropogenic NOx emissions show consistent annual variations over urban regions of the United States with a continuous decrease after 2011.
Yuli Cheng, Shanshan Wang, Jian Zhu, Yanlin Guo, Ruifeng Zhang, Yiming Liu, Yan Zhang, Qi Yu, Weichun Ma, and Bin Zhou
Atmos. Chem. Phys., 19, 13611–13626, https://doi.org/10.5194/acp-19-13611-2019, https://doi.org/10.5194/acp-19-13611-2019, 2019
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Owing to the gradual implementation of emission control zone (ECA) regulations, feasible technology for the surveillance of compliance with respect to fuel sulfur content is in high demand. We presented shore-based MAX-DOAS measurements of ship-emitted SO2 and NO2 under different traffic conditions. The results of this study indicate that this technique has high potential as a fast and accurate way to surveil ship emissions and fuel sulfur content.
Helen M. Worden, A. Anthony Bloom, John R. Worden, Zhe Jiang, Eloise A. Marais, Trissevgeni Stavrakou, Benjamin Gaubert, and Forrest Lacey
Atmos. Chem. Phys., 19, 13569–13579, https://doi.org/10.5194/acp-19-13569-2019, https://doi.org/10.5194/acp-19-13569-2019, 2019
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Biogenic non-methane volatile organic compounds (NMVOCs) emitted from vegetation play a significant role in air quality and climate. However, there are large uncertainties in their role for climate. We present a Bayesian approach to estimate carbon monoxide fluxes that are chemically produced from biogenic sources. This provides independent constraints on models that predict biogenic emissions in order improve their capability for predicting air quality and future climate scenarios.
Qindan Zhu, Joshua L. Laughner, and Ronald C. Cohen
Atmos. Chem. Phys., 19, 13067–13078, https://doi.org/10.5194/acp-19-13067-2019, https://doi.org/10.5194/acp-19-13067-2019, 2019
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Lightning NOx represents > 80 % of the NOx source in the upper troposphere. Despite its importance, lightning NOx is poorly understood. This work improves model performance in representing lighting NOx and reduces the uncertainty in satellite NO2 retrievals caused by poor representation of lightning NOx emissions in a priori assumptions.
Lisa K. Behrens, Andreas Hilboll, Andreas Richter, Enno Peters, Leonardo M. A. Alvarado, Anna B. Kalisz Hedegaard, Folkard Wittrock, John P. Burrows, and Mihalis Vrekoussis
Atmos. Chem. Phys., 19, 10257–10278, https://doi.org/10.5194/acp-19-10257-2019, https://doi.org/10.5194/acp-19-10257-2019, 2019
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MAX-DOAS measurements were conducted on the research vessel Maria S. Merian during a cruise from the Azores to South Africa in October 2016. The measurements indicate enhanced levels of HCHO and CHOCHO over the remote Atlantic Ocean, which is unexpected due to their short lifetime. Precursors of these gases or gas–aerosol combinations might be transported. Model simulations indicate potential source regions over the African continent, probably related to biomass burning or biogenic emissions.
Jacob C. A. van Peet and Ronald J. van der A
Atmos. Chem. Phys., 19, 8297–8309, https://doi.org/10.5194/acp-19-8297-2019, https://doi.org/10.5194/acp-19-8297-2019, 2019
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In this research, we combine satellite measurements of ozone with a chemical transport model of the atmosphere. The focus is on the ozone concentration between the surface and 6 km above mean sea level, since in that altitude range ozone has the highest impact on living organisms. Monthly mean ozone fields show significant improvements and more detail, especially for features such as biomass-burning-enhanced ozone concentrations and outflow of ozone-rich air from Asia over the Pacific.
Wenjing Su, Cheng Liu, Qihou Hu, Shaohua Zhao, Youwen Sun, Wei Wang, Yizhi Zhu, Jianguo Liu, and Jhoon Kim
Atmos. Chem. Phys., 19, 6717–6736, https://doi.org/10.5194/acp-19-6717-2019, https://doi.org/10.5194/acp-19-6717-2019, 2019
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For a better understanding of HCHO pollution and atmospheric chemistry, we evaluated primary and secondary sources of HCHO in the Yangtze River Delta based on HCHO column density from OMPS and combined this with in situ surface measurements. We found that secondary formation contributed most to ambient HCHO over longer timescales, but primary emission could be dominant in the winter. Hence, the usability of total HCHO as a proxy of VOC reactivity depends on the timescale of interest.
Lu Shen, Daniel J. Jacob, Xiong Liu, Guanyu Huang, Ke Li, Hong Liao, and Tao Wang
Atmos. Chem. Phys., 19, 6551–6560, https://doi.org/10.5194/acp-19-6551-2019, https://doi.org/10.5194/acp-19-6551-2019, 2019
Stefan F. Schreier, Andreas Richter, and John P. Burrows
Atmos. Chem. Phys., 19, 5853–5879, https://doi.org/10.5194/acp-19-5853-2019, https://doi.org/10.5194/acp-19-5853-2019, 2019
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In this case stuy, we have coupled ground-based remote-sensing measurements with surface in situ measurements to investigate NO2 distributions in the planetary boundary layer in the Viennese metropolitan area. We find that the application of a novel linear regression analysis for the conversion of tropospheric NO2 vertical columns into near-surface NO2 mixing ratios is promising and thus the method needs to be further explored and tested on satellite observations in future studies.
Yang Wang, Steffen Dörner, Sebastian Donner, Sebastian Böhnke, Isabelle De Smedt, Russell R. Dickerson, Zipeng Dong, Hao He, Zhanqing Li, Zhengqiang Li, Donghui Li, Dong Liu, Xinrong Ren, Nicolas Theys, Yuying Wang, Yang Wang, Zhenzhu Wang, Hua Xu, Jiwei Xu, and Thomas Wagner
Atmos. Chem. Phys., 19, 5417–5449, https://doi.org/10.5194/acp-19-5417-2019, https://doi.org/10.5194/acp-19-5417-2019, 2019
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A MAX-DOAS instrument was operated to derive tropospheric vertical profiles of NO2, SO2, HONO, HCHO, CHOCHO and aerosols in the central western North China Plain in May and June 2016. The MAX-DOAS results are verified by comparisons with a collocated Raman lidar, overpass aircraft measurements, a sun photometer and in situ measurements. The contributions of regional transports and local emissions to the pollutants are evaluated based on case studies and statistic analysis.
Wenfu Tang, Avelino F. Arellano, Benjamin Gaubert, Kazuyuki Miyazaki, and Helen M. Worden
Atmos. Chem. Phys., 19, 4269–4288, https://doi.org/10.5194/acp-19-4269-2019, https://doi.org/10.5194/acp-19-4269-2019, 2019
Iris N. Dekker, Sander Houweling, Sudhanshu Pandey, Maarten Krol, Thomas Röckmann, Tobias Borsdorff, Jochen Landgraf, and Ilse Aben
Atmos. Chem. Phys., 19, 3433–3445, https://doi.org/10.5194/acp-19-3433-2019, https://doi.org/10.5194/acp-19-3433-2019, 2019
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During November 2017, very high pollution levels were measured in the northern part of India. In this study, satellite (TROPOMI) data and model (WRF) data on carbon monoxide (CO) are studied to investigate the main sources of the CO pollution over the Indo-Gangetic Plain. We found that residential and commercial combustion was a much more important source of CO than the post-monsoon crop burning during this period. Meteorology was found important in the accumulation and ventilation of CO.
Cristen Adams, Chris A. McLinden, Mark W. Shephard, Nolan Dickson, Enrico Dammers, Jack Chen, Paul Makar, Karen E. Cady-Pereira, Naomi Tam, Shailesh K. Kharol, Lok N. Lamsal, and Nickolay A. Krotkov
Atmos. Chem. Phys., 19, 2577–2599, https://doi.org/10.5194/acp-19-2577-2019, https://doi.org/10.5194/acp-19-2577-2019, 2019
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We estimated how much carbon monoxide, ammonia, and nitrogen oxides were emitted in the smoke from the Fort McMurray Horse River wildfire using satellite data and air quality models. The fire emitted amounts of carbon monoxide that were similar to anthropogenic (human-caused) emissions for all of Alberta over a full year. We also estimated large amounts of ammonia and nitrogen oxides emitted from the fire. These results can be used to evaluate the performance of air quality forecasting models.
Daniel L. Goldberg, Pablo E. Saide, Lok N. Lamsal, Benjamin de Foy, Zifeng Lu, Jung-Hun Woo, Younha Kim, Jinseok Kim, Meng Gao, Gregory Carmichael, and David G. Streets
Atmos. Chem. Phys., 19, 1801–1818, https://doi.org/10.5194/acp-19-1801-2019, https://doi.org/10.5194/acp-19-1801-2019, 2019
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Using satellite data, we are able to estimate the emissions of NOx (NOx=NO+NO2), a toxic group of air pollutants, in the Seoul metropolitan area. We first develop an enhanced satellite product that better observes NO2 in urban regions. Using this new product, we derive NOx emissions to be twice as large as the emissions reported by the South Korean government. The implication is that the measures taken to reduce NOx emissions in South Korea have not been as effective as regulators have thought.
Michael Buchwitz, Maximilian Reuter, Oliver Schneising, Stefan Noël, Bettina Gier, Heinrich Bovensmann, John P. Burrows, Hartmut Boesch, Jasdeep Anand, Robert J. Parker, Peter Somkuti, Rob G. Detmers, Otto P. Hasekamp, Ilse Aben, André Butz, Akihiko Kuze, Hiroshi Suto, Yukio Yoshida, David Crisp, and Christopher O'Dell
Atmos. Chem. Phys., 18, 17355–17370, https://doi.org/10.5194/acp-18-17355-2018, https://doi.org/10.5194/acp-18-17355-2018, 2018
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We present a new satellite data set of column-averaged mixing ratios of carbon dioxide (CO2), which covers the time period 2003 to 2016. We used this data set to compute annual mean atmospheric CO2 growth rates. We show that the growth rate is highest during 2015 and 2016 despite nearly constant CO2 emissions from fossil fuel burning in recent years. The high growth rates are attributed to year 2015-2016 El Nino episodes. We present correlations with fossil fuel emissions and ENSO indices.
Fei Liu, Sungyeon Choi, Can Li, Vitali E. Fioletov, Chris A. McLinden, Joanna Joiner, Nickolay A. Krotkov, Huisheng Bian, Greet Janssens-Maenhout, Anton S. Darmenov, and Arlindo M. da Silva
Atmos. Chem. Phys., 18, 16571–16586, https://doi.org/10.5194/acp-18-16571-2018, https://doi.org/10.5194/acp-18-16571-2018, 2018
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Sulfur dioxide measurements from space have been used to detect emissions from large sources. We developed a new emission inventory by combining the satellite-based emission estimates and the conventional bottom-up inventory for smaller sources. The new inventory improves the model agreement with in situ observations and offers the possibility of rapid updates to emissions.
Gaëlle Dufour, Maxim Eremenko, Matthias Beekmann, Juan Cuesta, Gilles Foret, Audrey Fortems-Cheiney, Mathieu Lachâtre, Weili Lin, Yi Liu, Xiaobin Xu, and Yuli Zhang
Atmos. Chem. Phys., 18, 16439–16459, https://doi.org/10.5194/acp-18-16439-2018, https://doi.org/10.5194/acp-18-16439-2018, 2018
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The analysis of IASI lower tropospheric ozone columns over the North China Plain for the 2008–2016 period reveals two distinct periods: one before 2013 without any significant trend, and one after 2013 with a significant negative trend (−1.2 % yr−1). Our results suggest that the negative trend could be attributed to a reduction of the stratosphere-to-troposphere transport combined with the recent reduction of regional NOx emissions.
Jacob K. Hedelius, Junjie Liu, Tomohiro Oda, Shamil Maksyutov, Coleen M. Roehl, Laura T. Iraci, James R. Podolske, Patrick W. Hillyard, Jianming Liang, Kevin R. Gurney, Debra Wunch, and Paul O. Wennberg
Atmos. Chem. Phys., 18, 16271–16291, https://doi.org/10.5194/acp-18-16271-2018, https://doi.org/10.5194/acp-18-16271-2018, 2018
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Human activities can cause concentrated emissions of greenhouse gases and other pollutants from cities. There is ongoing effort to convert new satellite observations of pollutants into fluxes for many cities. Here we present a method for determining the flux of three species (CO2, CH4, and CO) from the greater LA area using satellite (CO2 only) and ground-based (all three species) observations. We run tests to estimate uncertainty and find the direct net CO2 flux is 104 ± 26 Tg CO2 yr−1.
Yuzhong Zhang, Daniel J. Jacob, Joannes D. Maasakkers, Melissa P. Sulprizio, Jian-Xiong Sheng, Ritesh Gautam, and John Worden
Atmos. Chem. Phys., 18, 15959–15973, https://doi.org/10.5194/acp-18-15959-2018, https://doi.org/10.5194/acp-18-15959-2018, 2018
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We assess the potential of using satellite observations of atmospheric methane to monitor global mean tropospheric OH concentration, a key parameter for the oxidizing power of the atmosphere.
Wei Tan, Cheng Liu, Shanshan Wang, Chengzhi Xing, Wenjing Su, Chengxin Zhang, Congzi Xia, Haoran Liu, Zhaonan Cai, and Jianguo Liu
Atmos. Chem. Phys., 18, 15387–15402, https://doi.org/10.5194/acp-18-15387-2018, https://doi.org/10.5194/acp-18-15387-2018, 2018
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This ship-based observation in June 2017 has, for the first time, reported the vertical column densities of NO2, SO2, and HCHO over oceanic areas of the East China Sea, which show good agreement with satellite observations. High levels of trace gases over oceanic areas were identified to be related to the regional transport of air pollutants from continental areas and nearby ship emissions.
Hansen Cao, Tzung-May Fu, Lin Zhang, Daven K. Henze, Christopher Chan Miller, Christophe Lerot, Gonzalo González Abad, Isabelle De Smedt, Qiang Zhang, Michel van Roozendael, François Hendrick, Kelly Chance, Jie Li, Junyu Zheng, and Yuanhong Zhao
Atmos. Chem. Phys., 18, 15017–15046, https://doi.org/10.5194/acp-18-15017-2018, https://doi.org/10.5194/acp-18-15017-2018, 2018
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Our top-down estimates for annual total Chinese NMVOC emissions was 30.7 to 49.5 Tg y−1, including 16.4 to 23.6 Tg y−1 from anthropogenic sources, 12.2 to 22.8 Tg y−1 from biogenic sources, and 2.08 to 3.13 Tg y−1 from biomass burning. Our four inversions consistently showed that the emissions of Chinese anthropogenic NMVOC precursors of glyoxal were larger than the a priori estimates. The glyoxal and formaldehyde constraints helped distinguish the NMVOC species from different sources.
Aldona Wiacek, Li Li, Keane Tobin, and Morgan Mitchell
Atmos. Chem. Phys., 18, 13787–13812, https://doi.org/10.5194/acp-18-13787-2018, https://doi.org/10.5194/acp-18-13787-2018, 2018
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Trace gas concentrations were measured at Halifax Harbour – an intermediate harbour integrated into the downtown core. We observed extended (~ 9 h) emission accumulations and also calculated marine sector emissions in the harbour. Regulated trace gas emissions were 2.8 % higher during cruise ship season (cruise ships contributed 18 % of emissions in season). Shipping NOx emissions were 4.2 times greater than those of a nearby 500 MW stationary source and were comparable to vehicle NOx emissions.
Juan Cuesta, Yugo Kanaya, Masayuki Takigawa, Gaëlle Dufour, Maxim Eremenko, Gilles Foret, Kazuyuki Miyazaki, and Matthias Beekmann
Atmos. Chem. Phys., 18, 9499–9525, https://doi.org/10.5194/acp-18-9499-2018, https://doi.org/10.5194/acp-18-9499-2018, 2018
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This paper tackles a major issue for air quality over East Asia: ozone pollution produced over a major source, like the North China Plain, and the contribution of ozone produced while being transported across the continent and the surrounding seas. The main originality of the paper lays in the fact that this photochemical production of ozone is observationally quantified with new multispectral satellite observations offering unique skills to observe the ozone pollution plumes near the surface.
Richard J. Pope, Martyn P. Chipperfield, Stephen R. Arnold, Norbert Glatthor, Wuhu Feng, Sandip S. Dhomse, Brian J. Kerridge, Barry G. Latter, and Richard Siddans
Atmos. Chem. Phys., 18, 8389–8408, https://doi.org/10.5194/acp-18-8389-2018, https://doi.org/10.5194/acp-18-8389-2018, 2018
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.
Catherine Wespes, Daniel Hurtmans, Cathy Clerbaux, Anne Boynard, and Pierre-François Coheur
Atmos. Chem. Phys., 18, 6867–6885, https://doi.org/10.5194/acp-18-6867-2018, https://doi.org/10.5194/acp-18-6867-2018, 2018
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.
Emily V. Fischer, Liye Zhu, Vivienne H. Payne, John R. Worden, Zhe Jiang, Susan S. Kulawik, Steven Brey, Arsineh Hecobian, Daniel Gombos, Karen Cady-Pereira, and Frank Flocke
Atmos. Chem. Phys., 18, 5639–5653, https://doi.org/10.5194/acp-18-5639-2018, https://doi.org/10.5194/acp-18-5639-2018, 2018
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PAN is an atmospheric reservoir for nitrogen oxide radicals, and it plays a lead role in their redistribution in the troposphere. We analyze new Tropospheric Emission Spectrometer (TES) PAN observations over North America during July 2006 to 2009. We identify smoke-impacted TES PAN retrievals by co-location with NOAA Hazard Mapping System (HMS) smoke plumes. Depending on the year, 15–32 % of cases where elevated PAN is identified in TES observations overlap with smoke plumes.
Luke Surl, Paul I. Palmer, and Gonzalo González Abad
Atmos. Chem. Phys., 18, 4549–4566, https://doi.org/10.5194/acp-18-4549-2018, https://doi.org/10.5194/acp-18-4549-2018, 2018
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We used observations of HCHO formaldehyde columns from the OMI satellite instrument and the GEOS-Chem atmospheric chemistry model to investigate how and why HCHO varies over India. We find that emissions of biogenic VOC from forests are the most powerful driver, with forests' response to seasonal temperature variations causing variation over time. Human-driven emissions of VOC and burning of vegetation have detectable, but more limited, impacts.
Luis F. Millán, Nathaniel J. Livesey, Michelle L. Santee, and Thomas von Clarmann
Atmos. Chem. Phys., 18, 4187–4199, https://doi.org/10.5194/acp-18-4187-2018, https://doi.org/10.5194/acp-18-4187-2018, 2018
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This study investigates orbital sampling biases and evaluates the additional impact caused by data quality screening for the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) and the Aura Microwave Limb Sounder (MLS).
Jacob C. A. van Peet, Ronald J. van der A, Hennie M. Kelder, and Pieternel F. Levelt
Atmos. Chem. Phys., 18, 1685–1704, https://doi.org/10.5194/acp-18-1685-2018, https://doi.org/10.5194/acp-18-1685-2018, 2018
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Ozone profiles measured by two satellite instruments (GOME-2A and OMI) have been combined with a chemical transport model using data assimilation. The results give a better insight into the global spatial and temporal ozone distribution than either measurement or model results alone. Validation with independent measurements shows biases varying between -5 % and +10 % between the surface and 100 hPa, while between 100 and 10 hPa the biases vary between -3 % and +3 %.
Uri Dayan, Philippe Ricaud, Régina Zbinden, and François Dulac
Atmos. Chem. Phys., 17, 13233–13263, https://doi.org/10.5194/acp-17-13233-2017, https://doi.org/10.5194/acp-17-13233-2017, 2017
Vitali Fioletov, Chris A. McLinden, Shailesh K. Kharol, Nickolay A. Krotkov, Can Li, Joanna Joiner, Michael D. Moran, Robert Vet, Antoon J. H. Visschedijk, and Hugo A. C. Denier van der Gon
Atmos. Chem. Phys., 17, 12597–12616, https://doi.org/10.5194/acp-17-12597-2017, https://doi.org/10.5194/acp-17-12597-2017, 2017
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