Articles | Volume 14, issue 22
https://doi.org/10.5194/acp-14-12373-2014
© Author(s) 2014. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Special issue:
https://doi.org/10.5194/acp-14-12373-2014
© Author(s) 2014. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Research article
| 
26 Nov 2014
Research article |
| 26 Nov 2014
Measurements of OH and RO2 radicals at Dome C, East Antarctica
A. Kukui
CORRESPONDING AUTHOR
Laboratoire Atmosphère, Milieux et Observations Spatiales (LATMOS), UMR8190, CNRS-Université de Versailles Saint Quentin, Université Pierre et Marie Curie, Paris, France
Laboratoire de Physique et Chimie de l'Environnement et de l'Espace (LPC2E), UMR6115, CNRS–Université d'Orléans, 45071 Orléans CEDEX 2, France
M. Legrand
Laboratoire de Glaciologie et Géophysique de l'Environnement (LGGE), UMR5183, CNRS-Université Grenoble Alpes, Grenoble, France
S. Preunkert
Laboratoire de Glaciologie et Géophysique de l'Environnement (LGGE), UMR5183, CNRS-Université Grenoble Alpes, Grenoble, France
M. M. Frey
British Antarctic Survey (BAS), Natural Environment Research Council (NERC), Cambridge, UK
R. Loisil
Division Technique (UPS855) de l'Institut National des Sciences de l'Univers (INSU), Meudon, France
J. Gil Roca
Laboratoire Atmosphère, Milieux et Observations Spatiales (LATMOS), UMR8190, CNRS-Université de Versailles Saint Quentin, Université Pierre et Marie Curie, Paris, France
B. Jourdain
Laboratoire de Glaciologie et Géophysique de l'Environnement (LGGE), UMR5183, CNRS-Université Grenoble Alpes, Grenoble, France
M. D. King
Department of Earth Sciences, Royal Holloway University of London, Egham, Surrey, TW20 OEX, UK
J. L. France
Department of Earth Sciences, Royal Holloway University of London, Egham, Surrey, TW20 OEX, UK
G. Ancellet
Laboratoire Atmosphère, Milieux et Observations Spatiales (LATMOS), UMR8190, CNRS-Université de Versailles Saint Quentin, Université Pierre et Marie Curie, Paris, France
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Maxim L. Lamare, John D. Hedley, and Martin D. King
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Albane Barbero, Roberto Grilli, Markus M. Frey, Camille Blouzon, Detlev Helmig, Nicolas Caillon, and Joël Savarino
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The high reactivity of the summer Antarctic boundary layer results in part from the emissions of nitrogen oxides produced during photo-denitrification of the snowpack, but its underlying mechanisms are not yet fully understood. The results of this study suggest that more NO2 is produced from the snowpack early in the photolytic season, possibly due to stronger UV irradiance caused by a smaller solar zenith angle near the solstice.
Sophie Godin-Beekmann, Niramson Azouz, Viktoria F. Sofieva, Daan Hubert, Irina Petropavlovskikh, Peter Effertz, Gérard Ancellet, Doug A. Degenstein, Daniel Zawada, Lucien Froidevaux, Stacey Frith, Jeannette Wild, Sean Davis, Wolfgang Steinbrecht, Thierry Leblanc, Richard Querel, Kleareti Tourpali, Robert Damadeo, Eliane Maillard Barras, René Stübi, Corinne Vigouroux, Carlo Arosio, Gerald Nedoluha, Ian Boyd, Roeland Van Malderen, Emmanuel Mahieu, Dan Smale, and Ralf Sussmann
Atmos. Chem. Phys., 22, 11657–11673, https://doi.org/10.5194/acp-22-11657-2022, https://doi.org/10.5194/acp-22-11657-2022, 2022
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An updated evaluation up to 2020 of stratospheric ozone profile long-term trends at extrapolar latitudes based on satellite and ground-based records is presented. Ozone increase in the upper stratosphere is confirmed, with significant trends at most latitudes. In this altitude region, a very good agreement is found with trends derived from chemistry–climate model simulations. Observed and modelled trends diverge in the lower stratosphere, but the differences are non-significant.
Silvia Becagli, Elena Barbaro, Simone Bonamano, Laura Caiazzo, Alcide di Sarra, Matteo Feltracco, Paolo Grigioni, Jost Heintzenberg, Luigi Lazzara, Michel Legrand, Alice Madonia, Marco Marcelli, Chiara Melillo, Daniela Meloni, Caterina Nuccio, Giandomenico Pace, Ki-Tae Park, Suzanne Preunkert, Mirko Severi, Marco Vecchiato, Roberta Zangrando, and Rita Traversi
Atmos. Chem. Phys., 22, 9245–9263, https://doi.org/10.5194/acp-22-9245-2022, https://doi.org/10.5194/acp-22-9245-2022, 2022
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Measurements of phytoplanktonic dimethylsulfide and its oxidation products in the Antarctic atmosphere allow us to understand the role of the oceanic (sea ice melting, Chl α and dimethylsulfoniopropionate) and atmospheric (wind direction and speed, humidity, solar radiation and transport processes) factors in the biogenic aerosol formation, concentration and characteristic ratio between components in an Antarctic coastal site facing the polynya of the Ross Sea.
Boris D. Belan, Gerard Ancellet, Irina S. Andreeva, Pavel N. Antokhin, Viktoria G. Arshinova, Mikhail Y. Arshinov, Yurii S. Balin, Vladimir E. Barsuk, Sergei B. Belan, Dmitry G. Chernov, Denis K. Davydov, Alexander V. Fofonov, Georgii A. Ivlev, Sergei N. Kotel'nikov, Alexander S. Kozlov, Artem V. Kozlov, Katharine Law, Andrey V. Mikhal'chishin, Igor A. Moseikin, Sergei V. Nasonov, Philippe Nédélec, Olesya V. Okhlopkova, Sergei E. Ol'kin, Mikhail V. Panchenko, Jean-Daniel Paris, Iogannes E. Penner, Igor V. Ptashnik, Tatyana M. Rasskazchikova, Irina K. Reznikova, Oleg A. Romanovskii, Alexander S. Safatov, Denis E. Savkin, Denis V. Simonenkov, Tatyana K. Sklyadneva, Gennadii N. Tolmachev, Semyon V. Yakovlev, and Polina N. Zenkova
Atmos. Meas. Tech., 15, 3941–3967, https://doi.org/10.5194/amt-15-3941-2022, https://doi.org/10.5194/amt-15-3941-2022, 2022
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The change of the global climate is most pronounced in the Arctic, where the air temperature increases faster than the global average. This is associated with an increase in the concentration of greenhouse gases in the atmosphere. It is important to study how the air composition in the Arctic changes in the changing climate. Thus this integrated experiment was carried out to measure the composition of the troposphere in the Russian sector of the Arctic from on board the aircraft laboratory.
David N. Wagner, Matthew D. Shupe, Christopher Cox, Ola G. Persson, Taneil Uttal, Markus M. Frey, Amélie Kirchgaessner, Martin Schneebeli, Matthias Jaggi, Amy R. Macfarlane, Polona Itkin, Stefanie Arndt, Stefan Hendricks, Daniela Krampe, Marcel Nicolaus, Robert Ricker, Julia Regnery, Nikolai Kolabutin, Egor Shimanshuck, Marc Oggier, Ian Raphael, Julienne Stroeve, and Michael Lehning
The Cryosphere, 16, 2373–2402, https://doi.org/10.5194/tc-16-2373-2022, https://doi.org/10.5194/tc-16-2373-2022, 2022
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Based on measurements of the snow cover over sea ice and atmospheric measurements, we estimate snowfall and snow accumulation for the MOSAiC ice floe, between November 2019 and May 2020. For this period, we estimate 98–114 mm of precipitation. We suggest that about 34 mm of snow water equivalent accumulated until the end of April 2020 and that at least about 50 % of the precipitated snow was eroded or sublimated. Further, we suggest explanations for potential snowfall overestimation.
Gérard Ancellet, Sophie Godin-Beekmann, Herman G. J. Smit, Ryan M. Stauffer, Roeland Van Malderen, Renaud Bodichon, and Andrea Pazmiño
Atmos. Meas. Tech., 15, 3105–3120, https://doi.org/10.5194/amt-15-3105-2022, https://doi.org/10.5194/amt-15-3105-2022, 2022
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The 1991–2021 Observatoire de Haute Provence electrochemical concentration cell (ECC) ozonesonde data have been homogenized according to the recommendations of the Ozonesonde Data Quality Assessment panel. Comparisons with ground-based instruments also measuring ozone at the same station (lidar, surface measurements) and with colocated satellite observations show the benefits of this homogenization. Remaining differences between ECC and other observations in the stratosphere are also discussed.
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.
Xavier Faïn, Rachael H. Rhodes, Philip Place, Vasilii V. Petrenko, Kévin Fourteau, Nathan Chellman, Edward Crosier, Joseph R. McConnell, Edward J. Brook, Thomas Blunier, Michel Legrand, and Jérôme Chappellaz
Clim. Past, 18, 631–647, https://doi.org/10.5194/cp-18-631-2022, https://doi.org/10.5194/cp-18-631-2022, 2022
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Carbon monoxide (CO) is a regulated pollutant and one of the key components determining the oxidizing capacity of the atmosphere. In this study, we analyzed five ice cores from Greenland at high resolution for CO concentrations by coupling laser spectrometry with continuous melting. By combining these new datasets, we produced an upper-bound estimate of past atmospheric CO abundance since preindustrial times for the Northern Hemisphere high latitudes, covering the period from 1700 to 1957 CE.
Thibault Vaillant de Guélis, Gérard Ancellet, Anne Garnier, Laurent C.-Labonnote, Jacques Pelon, Mark A. Vaughan, Zhaoyan Liu, and David M. Winker
Atmos. Meas. Tech., 15, 1931–1956, https://doi.org/10.5194/amt-15-1931-2022, https://doi.org/10.5194/amt-15-1931-2022, 2022
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A new IIR-based cloud and aerosol discrimination (CAD) algorithm is developed using the IIR brightness temperature differences for cloud and aerosol features confidently identified by the CALIOP version 4 CAD algorithm. IIR classifications agree with the majority of V4 cloud identifications, reduce the ambiguity in a notable fraction of
not confidentV4 cloud classifications, and correct a few V4 misclassifications of cloud layers identified as dense dust or elevated smoke layers by CALIOP.
Irina Petropavlovskikh, Koji Miyagawa, Audra McClure-Beegle, Bryan Johnson, Jeannette Wild, Susan Strahan, Krzysztof Wargan, Richard Querel, Lawrence Flynn, Eric Beach, Gerard Ancellet, and Sophie Godin-Beekmann
Atmos. Meas. Tech., 15, 1849–1870, https://doi.org/10.5194/amt-15-1849-2022, https://doi.org/10.5194/amt-15-1849-2022, 2022
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The Montreal Protocol and its amendments assure the recovery of the stratospheric ozone layer that protects the Earth from harmful ultraviolet radiation. To monitor ozone recovery, multiple satellites and ground-based observational platforms collect ozone data. The changes in instruments can influence the continuation of the ozone data. We discuss a method to remove instrumental artifacts from ozone records to improve the internal consistency among multiple observational records.
Alexandre Kukui, Michel Chartier, Jinhe Wang, Hui Chen, Sébastien Dusanter, Stéphane Sauvage, Vincent Michoud, Nadine Locoge, Valérie Gros, Thierry Bourrianne, Karine Sellegri, and Jean-Marc Pichon
Atmos. Chem. Phys., 21, 13333–13351, https://doi.org/10.5194/acp-21-13333-2021, https://doi.org/10.5194/acp-21-13333-2021, 2021
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Sulfuric acid, H2SO4, plays a key role in formation of secondary atmospheric aerosol particles. It is generally accepted that the major atmospheric source of H2SO4 is the reaction of OH radicals with SO2. In this study, importance of an additional H2SO4 source via oxidation of SO2 by stabilized Criegee intermediates was estimated based on measurements at a remote site on Cape Corsica. It was found that the oxidation of SO2 by SCI may be an important source of H2SO4, especially during nighttime.
Robin Wing, Wolfgang Steinbrecht, Sophie Godin-Beekmann, Thomas J. McGee, John T. Sullivan, Grant Sumnicht, Gérard Ancellet, Alain Hauchecorne, Sergey Khaykin, and Philippe Keckhut
Atmos. Meas. Tech., 13, 5621–5642, https://doi.org/10.5194/amt-13-5621-2020, https://doi.org/10.5194/amt-13-5621-2020, 2020
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A lidar intercomparison campaign was conducted over a period of 28 nights at Observatoire de Haute-Provence (OHP) in 2017 and 2018. The objective is to validate the ozone and temperature profiles at OHP to ensure the quality of data submitted to the NDACC database remains high. A mobile reference lidar operated by NASA was transported to OHP and operated concurrently with the French lidars. Agreement for ozone was better than 5 % between 20 and 40 km, and temperatures were equal within 3 K.
Tuukka Petäjä, Ella-Maria Duplissy, Ksenia Tabakova, Julia Schmale, Barbara Altstädter, Gerard Ancellet, Mikhail Arshinov, Yurii Balin, Urs Baltensperger, Jens Bange, Alison Beamish, Boris Belan, Antoine Berchet, Rossana Bossi, Warren R. L. Cairns, Ralf Ebinghaus, Imad El Haddad, Beatriz Ferreira-Araujo, Anna Franck, Lin Huang, Antti Hyvärinen, Angelika Humbert, Athina-Cerise Kalogridis, Pavel Konstantinov, Astrid Lampert, Matthew MacLeod, Olivier Magand, Alexander Mahura, Louis Marelle, Vladimir Masloboev, Dmitri Moisseev, Vaios Moschos, Niklas Neckel, Tatsuo Onishi, Stefan Osterwalder, Aino Ovaska, Pauli Paasonen, Mikhail Panchenko, Fidel Pankratov, Jakob B. Pernov, Andreas Platis, Olga Popovicheva, Jean-Christophe Raut, Aurélie Riandet, Torsten Sachs, Rosamaria Salvatori, Roberto Salzano, Ludwig Schröder, Martin Schön, Vladimir Shevchenko, Henrik Skov, Jeroen E. Sonke, Andrea Spolaor, Vasileios K. Stathopoulos, Mikko Strahlendorff, Jennie L. Thomas, Vito Vitale, Sterios Vratolis, Carlo Barbante, Sabine Chabrillat, Aurélien Dommergue, Konstantinos Eleftheriadis, Jyri Heilimo, Kathy S. Law, Andreas Massling, Steffen M. Noe, Jean-Daniel Paris, André S. H. Prévôt, Ilona Riipinen, Birgit Wehner, Zhiyong Xie, and Hanna K. Lappalainen
Atmos. Chem. Phys., 20, 8551–8592, https://doi.org/10.5194/acp-20-8551-2020, https://doi.org/10.5194/acp-20-8551-2020, 2020
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The role of polar regions is increasing in terms of megatrends such as globalization, new transport routes, demography, and the use of natural resources with consequent effects on regional and transported pollutant concentrations. Here we summarize initial results from our integrative project exploring the Arctic environment and pollution to deliver data products, metrics, and indicators for stakeholders.
V. Holly L. Winton, Alison Ming, Nicolas Caillon, Lisa Hauge, Anna E. Jones, Joel Savarino, Xin Yang, and Markus M. Frey
Atmos. Chem. Phys., 20, 5861–5885, https://doi.org/10.5194/acp-20-5861-2020, https://doi.org/10.5194/acp-20-5861-2020, 2020
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The transfer of the nitrogen stable isotopic composition in nitrate between the air and snow at low accumulation sites in Antarctica leaves an UV imprint in the snow. Quantifying how nitrate isotope values change allows us to interpret longer ice core records. Based on nitrate observations and modelling at Kohnen, East Antarctica, the dominant factors controlling the nitrate isotope signature in deep snow layers are the depth of light penetration into the snowpack and the snow accumulation rate.
Antonin Zabukovec, Gerard Ancellet, Iwan E. Penner, Mikhail Arshinov, Valery Kozlov, Jacques Pelon, Jean-Daniel Paris, Grigory Kokhanenko, Yuri S. Balin, Dmitry Chernov, and Boris D. Belan
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2020-195, https://doi.org/10.5194/acp-2020-195, 2020
Preprint withdrawn
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Description of two aircraft campaigns results carried out over Siberia in 2013 and 2017 to characterize aerosol emission. A methodology is proposed to derive the aerosol types using transport model and satellite observations. The extinction to backscatter ratio for each aerosol types is reported as it is a key parameter to constrain their radiative impact. These results are compared to previous work conducted in other regions and to aerosol data products observed by spaceborne lidars.
Markus M. Frey, Sarah J. Norris, Ian M. Brooks, Philip S. Anderson, Kouichi Nishimura, Xin Yang, Anna E. Jones, Michelle G. Nerentorp Mastromonaco, David H. Jones, and Eric W. Wolff
Atmos. Chem. Phys., 20, 2549–2578, https://doi.org/10.5194/acp-20-2549-2020, https://doi.org/10.5194/acp-20-2549-2020, 2020
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A winter sea ice expedition to Antarctica provided the first direct observations of sea salt aerosol (SSA) production during snow storms above sea ice, thereby validating a model hypothesis to account for winter time SSA maxima in Antarctica not explained otherwise. Defining SSA sources is important given the critical roles that aerosol plays for climate, for air quality and as a potential ice core proxy for sea ice conditions in the past.
Susanne Preunkert, Michel Legrand, Stanislav Kutuzov, Patrick Ginot, Vladimir Mikhalenko, and Ronny Friedrich
Atmos. Chem. Phys., 19, 14119–14132, https://doi.org/10.5194/acp-19-14119-2019, https://doi.org/10.5194/acp-19-14119-2019, 2019
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This paper reports on an ice core drilled to bedrock at Mt Elbrus (5115 m a.s.l., Russia) to reconstruct the atmospheric pollution since the 19th century in south-eastern Europe. The annual dust-free sulfate record indicates a 7-fold increase from prior to 1900 to 1980–1995. Consistent with past SO2 emission inventories, a much earlier onset and a more pronounced decrease in the sulfur pollution over the last 3 decades are observed in western Europe than in south-eastern and eastern Europe.
Stanislav Kutuzov, Michel Legrand, Susanne Preunkert, Patrick Ginot, Vladimir Mikhalenko, Karim Shukurov, Aleksei Poliukhov, and Pavel Toropov
Atmos. Chem. Phys., 19, 14133–14148, https://doi.org/10.5194/acp-19-14133-2019, https://doi.org/10.5194/acp-19-14133-2019, 2019
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Ice cores are one of the most valuable paleo-archives. Here we present analysis of the concentrations of calcium, recorded in ice core from the Caucasus over the past 240 years. We found a correlation between dust in ice and precipitation and soil moisture content in the Middle East and North Africa. The prominent increase in dust concentration in the ice core confirms that the recent droughts in the Fertile Crescent were most severe at least for the past two centuries.
Xin Yang, Markus M. Frey, Rachael H. Rhodes, Sarah J. Norris, Ian M. Brooks, Philip S. Anderson, Kouichi Nishimura, Anna E. Jones, and Eric W. Wolff
Atmos. Chem. Phys., 19, 8407–8424, https://doi.org/10.5194/acp-19-8407-2019, https://doi.org/10.5194/acp-19-8407-2019, 2019
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This is a comprehensive model–data comparison aiming to evaluate the proposed mechanism of sea salt aerosol (SSA) production from blowing snow on sea ice. Some key parameters such as snow salinity and blowing-snow size distribution were constrained by data collected in the Weddell Sea. The good agreement between modelled SSA and the cruise data strongly indicates that sea ice surface is a large SSA source in polar regions, a process which has not been considered in current climate models.
Sentia Goursaud, Valérie Masson-Delmotte, Vincent Favier, Suzanne Preunkert, Michel Legrand, Bénédicte Minster, and Martin Werner
The Cryosphere, 13, 1297–1324, https://doi.org/10.5194/tc-13-1297-2019, https://doi.org/10.5194/tc-13-1297-2019, 2019
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We report new water stable isotope records from the first highly resolved firn core drilled in Adélie Land and covering 1998–2014. Using an updated database, we show that mean values are in line with the range of coastal values. Statistical analyses show no relationship between our record and local surface air temperature. Atmospheric back trajectories and isotopic simulations suggest that water stable isotopes in Adélie provide a fingerprint of the variability of atmospheric dynamics.
Leonie Bernet, Thomas von Clarmann, Sophie Godin-Beekmann, Gérard Ancellet, Eliane Maillard Barras, René Stübi, Wolfgang Steinbrecht, Niklaus Kämpfer, and Klemens Hocke
Atmos. Chem. Phys., 19, 4289–4309, https://doi.org/10.5194/acp-19-4289-2019, https://doi.org/10.5194/acp-19-4289-2019, 2019
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After severe ozone depletion, upper stratospheric ozone has started to recover in recent years. However, stratospheric ozone trends from various data sets still show differences. To partly explain such differences, we investigate how the trends are affected by different factors, for example, anomalies in the data. We show how trend estimates can be improved by considering such anomalies and present updated stratospheric ozone trends from ground data measured in central Europe.
Gerard Ancellet, Iogannes E. Penner, Jacques Pelon, Vincent Mariage, Antonin Zabukovec, Jean Christophe Raut, Grigorii Kokhanenko, and Yuri S. Balin
Atmos. Meas. Tech., 12, 147–168, https://doi.org/10.5194/amt-12-147-2019, https://doi.org/10.5194/amt-12-147-2019, 2019
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Aerosol type seasonal variability and sources in Siberia are obtained from an automatic 808 nm micropulse lidar. A total of 540 aerosol backscatter vertical profiles have been retrieved using careful lidar calibration. Aerosol optical depth is retrieved using sun-photometer complementary observations and an aerosol source apportionment based on aerosol transport model simulations. Comparisons with satellite observations are discussed for three case studies.
Vincent Michoud, Stéphane Sauvage, Thierry Léonardis, Isabelle Fronval, Alexandre Kukui, Nadine Locoge, and Sébastien Dusanter
Atmos. Meas. Tech., 11, 5729–5740, https://doi.org/10.5194/amt-11-5729-2018, https://doi.org/10.5194/amt-11-5729-2018, 2018
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This study presents the first measurements of ambient methylglyoxal, an important atmospheric α-dicarbonyl, using proton transfer reaction time-of-flight mass spectrometry. These measurements mostly agree with concomitant measurements from a reference technique: the DNPH derivatization technique and high-performance liquid chromatography with UV detection. In addition, a careful investigation of the differences between the two techniques is carried out to explain the disagreements observed.
Ioana Elisabeta Popovici, Philippe Goloub, Thierry Podvin, Luc Blarel, Rodrigue Loisil, Florin Unga, Augustin Mortier, Christine Deroo, Stéphane Victori, Fabrice Ducos, Benjamin Torres, Cyril Delegove, Marie Choël, Nathalie Pujol-Söhne, and Christophe Pietras
Atmos. Meas. Tech., 11, 4671–4691, https://doi.org/10.5194/amt-11-4671-2018, https://doi.org/10.5194/amt-11-4671-2018, 2018
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This paper aims to show the potential of an instrumented mobile platform, performing on-road remote sensing and in situ measurements, to derive aerosol properties. It is distinguished from other transportable platforms through its ability to perform measurements during movement. Its reduced size, versatility and great flexibility makes it suitable for following sudden aerosol events and for validating satellite measurements and model simulations.
Rosalie H. Shepherd, Martin D. King, Amelia A. Marks, Neil Brough, and Andrew D. Ward
Atmos. Chem. Phys., 18, 5235–5252, https://doi.org/10.5194/acp-18-5235-2018, https://doi.org/10.5194/acp-18-5235-2018, 2018
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The refractive index of atmospheric extracts sourced from urban (London), remote (Antarctica), and woodsmoke aerosol was determined by applying optical trapping simultaneously with Mie spectroscopy. In addition, owing to the absorbing nature of woodsmoke and an aqueous humic acid aerosol extract, the absorption Ångström exponent could be determined.The refractive index and absorption Ångström exponent were then applied in a top-of-the-atmosphere albedo radiation transfer model.
Rolf Weller, Michel Legrand, and Susanne Preunkert
Atmos. Chem. Phys., 18, 2413–2430, https://doi.org/10.5194/acp-18-2413-2018, https://doi.org/10.5194/acp-18-2413-2018, 2018
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We measured aerosol size distributions and the composition of summer aerosol at the continental Antarctic station Kohnen. Two different weather conditions mediated the transport of aerosol: (1) the intermittent impact of cyclones associated with outstanding marine aerosol concentrations and new particle formation and (2) steady long-range transport under prevailing clear sky conditions. The latter air masses were characterized by aged aerosol and less aerosol load.
Hoi Ga Chan, Markus M. Frey, and Martin D. King
Atmos. Chem. Phys., 18, 1507–1534, https://doi.org/10.5194/acp-18-1507-2018, https://doi.org/10.5194/acp-18-1507-2018, 2018
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Emissions of reactive nitrogen from snowpacks influence remote air quality. Two physical air–snow models for nitrate were developed. One assumes that below a threshold temperature the air–snow grain interface is pure ice and above it a disordered interface emerges. The other assumes an air–ice interface below melting and that any liquid present is concentrated in micropockets. Only the latter matches observations at two Antarctic lcoations covering a wide range of environmental conditions.
Amelia A. Marks, Maxim L. Lamare, and Martin D. King
The Cryosphere, 11, 2867–2881, https://doi.org/10.5194/tc-11-2867-2017, https://doi.org/10.5194/tc-11-2867-2017, 2017
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Arctic sea ice extent is declining rapidly. Prediction of sea ice trends relies on sea ice models that need to be evaluated with real data. A realistic sea ice environment is created in a laboratory by the Royal Holloway sea ice simulator and is used to show a sea ice model can replicate measured properties of sea ice, e.g. reflectance. Black carbon, a component of soot found in atmospheric pollution, is also experimentally shown to reduce the sea ice reflectance, which could exacerbate melting.
Michel Legrand, Susanne Preunkert, Eric Wolff, Rolf Weller, Bruno Jourdain, and Dietmar Wagenbach
Atmos. Chem. Phys., 17, 14039–14054, https://doi.org/10.5194/acp-17-14039-2017, https://doi.org/10.5194/acp-17-14039-2017, 2017
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Multiple year-round records of bulk and size-segregated composition of sea-salt aerosol and acidic gases (HCl and HNO3) were obtained at inland Antarctica. Both acidic sulfur particles and nitric acid are involved in the observed sea-salt dechlorination in spring/summer. The observed sulfate to sodium mass ratio of sea-salt aerosol in winter (0.16 ± 0.05) suggests on average a similar contribution of sea-ice and open-ocean emissions to the sea-salt load over inland Antarctica at that season.
Michel Legrand, Susanne Preunkert, Rolf Weller, Lars Zipf, Christoph Elsässer, Silke Merchel, Georg Rugel, and Dietmar Wagenbach
Atmos. Chem. Phys., 17, 14055–14073, https://doi.org/10.5194/acp-17-14055-2017, https://doi.org/10.5194/acp-17-14055-2017, 2017
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Levels of MSA and sulfate at inland Antarctica are documented from multiple year-round records of bulk and size-segregated aerosol samplings. A striking difference in the seasonality of sulfur aerosol composition, characterized by a MSA to nssSO4 ratio reaching a minimum in summer over the Antarctic plateau (0.05) and a maximum at the coast (up to 0.40), is clearly established. An efficient chemical destruction of MSA is suggested to take place over the Antarctic plateau in summer.
Gwennolé Guyot, Frans Olofson, Peter Tunved, Christophe Gourbeyre, Guy Fevbre, Régis Dupuy, Christophe Bernard, Gérard Ancellet, Kathy Law, Boris Quennehen, Alfons Schwarzenboeck, Kostas Eleftheriadis, and Olivier Jourdan
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2017-672, https://doi.org/10.5194/acp-2017-672, 2017
Revised manuscript has not been submitted
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Cloud and aerosol properties are key parameters in the accelerated arctic warming. In this context, this study will focus on in situ cloud microphysical and optical characterization of arctic Mixed Phase Cloud combined with aerosol measurements and air mass backtrajectory simulations during the ground based CLIMSLIP-NyA campaign performed in Ny-Alesund, Svalbard. The goal is to parameterize the arctic aerosol-cloud interaction and assess the influence of anthropogenic pollution.
Rachael H. Rhodes, Xin Yang, Eric W. Wolff, Joseph R. McConnell, and Markus M. Frey
Atmos. Chem. Phys., 17, 9417–9433, https://doi.org/10.5194/acp-17-9417-2017, https://doi.org/10.5194/acp-17-9417-2017, 2017
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Sea salt aerosol comes from the open ocean or the sea ice surface. In the polar regions, this opens up the possibility of reconstructing sea ice history using sea salt recorded in ice cores. We use a chemical transport model to demonstrate that the sea ice source of aerosol is important in the Arctic. For the first time, we simulate realistic Greenland ice core sea salt in a process-based model. The importance of the sea ice source increases from south to north across the Greenland ice sheet.
Guanyu Huang, Xiong Liu, Kelly Chance, Kai Yang, Pawan K. Bhartia, Zhaonan Cai, Marc Allaart, Gérard Ancellet, Bertrand Calpini, Gerrie J. R. Coetzee, Emilio Cuevas-Agulló, Manuel Cupeiro, Hugo De Backer, Manvendra K. Dubey, Henry E. Fuelberg, Masatomo Fujiwara, Sophie Godin-Beekmann, Tristan J. Hall, Bryan Johnson, Everette Joseph, Rigel Kivi, Bogumil Kois, Ninong Komala, Gert König-Langlo, Giovanni Laneve, Thierry Leblanc, Marion Marchand, Kenneth R. Minschwaner, Gary Morris, Michael J. Newchurch, Shin-Ya Ogino, Nozomu Ohkawara, Ankie J. M. Piters, Françoise Posny, Richard Querel, Rinus Scheele, Frank J. Schmidlin, Russell C. Schnell, Otto Schrems, Henry Selkirk, Masato Shiotani, Pavla Skrivánková, René Stübi, Ghassan Taha, David W. Tarasick, Anne M. Thompson, Valérie Thouret, Matthew B. Tully, Roeland Van Malderen, Holger Vömel, Peter von der Gathen, Jacquelyn C. Witte, and Margarita Yela
Atmos. Meas. Tech., 10, 2455–2475, https://doi.org/10.5194/amt-10-2455-2017, https://doi.org/10.5194/amt-10-2455-2017, 2017
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It is essential to understand the data quality of +10-year OMI ozone product and impacts of the “row anomaly” (RA). We validate the OMI Ozone Profile (PROFOZ) product from Oct 2004 to Dec 2014 against ozonesonde observations globally. Generally, OMI has good agreement with ozonesondes. The spatiotemporal variation of retrieval performance suggests the need to improve OMI’s radiometric calibration especially during the post-RA period to maintain the long-term stability.
Anna Kozachek, Vladimir Mikhalenko, Valérie Masson-Delmotte, Alexey Ekaykin, Patrick Ginot, Stanislav Kutuzov, Michel Legrand, Vladimir Lipenkov, and Susanne Preunkert
Clim. Past, 13, 473–489, https://doi.org/10.5194/cp-13-473-2017, https://doi.org/10.5194/cp-13-473-2017, 2017
Sakiko Ishino, Shohei Hattori, Joel Savarino, Bruno Jourdain, Susanne Preunkert, Michel Legrand, Nicolas Caillon, Albane Barbero, Kota Kuribayashi, and Naohiro Yoshida
Atmos. Chem. Phys., 17, 3713–3727, https://doi.org/10.5194/acp-17-3713-2017, https://doi.org/10.5194/acp-17-3713-2017, 2017
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We show the first simultaneous observations of triple oxygen isotopic compositions of atmospheric sulfate, nitrate, and ozone at Dumont d'Urville, coastal Antarctica. The contrasting seasonal trends between oxygen isotopes of ozone and those of sulfate and nitrate indicate that these signatures in sulfate and nitrate are mainly controlled by changes in oxidation chemistry. We also discuss the specific oxidation chemistry induced by the unique phenomena at the site.
Sentia Goursaud, Valérie Masson-Delmotte, Vincent Favier, Susanne Preunkert, Michel Fily, Hubert Gallée, Bruno Jourdain, Michel Legrand, Olivier Magand, Bénédicte Minster, and Martin Werner
The Cryosphere, 11, 343–362, https://doi.org/10.5194/tc-11-343-2017, https://doi.org/10.5194/tc-11-343-2017, 2017
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Uncertainty of sea level changes is a challenge. As Antarctica is the biggest water reservoir, it is necessary to know how it will contribute. To be able to simulate it, an understanding of past climate is to be achieved, for instance, by studying the ice cores. As climate change is different in different regions, observations are needed all over the continent. Studying an ice core in Adélie Land, we can conclude that there are no changes there at decadal scale over the period 1947–2007.
Gerard Ancellet, Nikos Daskalakis, Jean Christophe Raut, David Tarasick, Jonathan Hair, Boris Quennehen, François Ravetta, Hans Schlager, Andrew J. Weinheimer, Anne M. Thompson, Bryan Johnson, Jennie L. Thomas, and Katharine S. Law
Atmos. Chem. Phys., 16, 13341–13358, https://doi.org/10.5194/acp-16-13341-2016, https://doi.org/10.5194/acp-16-13341-2016, 2016
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An integrated analysis of all the ozone observations (lidar, sondes, and airborne in situ measurements) conducted during the 2008 IPY campaigns is performed and the processes that determine summer ozone concentrations over Greenland and Canada are discussed. Combined with a regional model simulation (WRFChem), the analysis of ozone, CO, and PV latitudinal and vertical variability allows the determination of the influence of stratospheric sources and biomass burning and anthropogenic emissions.
Michel Legrand, Joseph McConnell, Hubertus Fischer, Eric W. Wolff, Susanne Preunkert, Monica Arienzo, Nathan Chellman, Daiana Leuenberger, Olivia Maselli, Philip Place, Michael Sigl, Simon Schüpbach, and Mike Flannigan
Clim. Past, 12, 2033–2059, https://doi.org/10.5194/cp-12-2033-2016, https://doi.org/10.5194/cp-12-2033-2016, 2016
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Here, we review previous attempts made to reconstruct past forest fire using chemical signals recorded in Greenland ice. We showed that the Greenland ice records of ammonium, found to be a good fire proxy, consistently indicate changing fire activity in Canada in response to past climatic conditions that occurred since the last 15 000 years, including the Little Ice Age and the last large climatic transition.
Claudia Di Biagio, Paola Formenti, Lionel Doppler, Cécile Gaimoz, Noel Grand, Gerard Ancellet, Jean-Luc Attié, Silvia Bucci, Philippe Dubuisson, Federico Fierli, Marc Mallet, and François Ravetta
Atmos. Chem. Phys., 16, 10591–10607, https://doi.org/10.5194/acp-16-10591-2016, https://doi.org/10.5194/acp-16-10591-2016, 2016
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Pollution aerosols strongly influence the composition of the Western Mediterranean, but at present little is known on their optical properties. Here, we report observations of pollution aerosols measured during the TRAQA airborne campaign in summer 2012. Data from this study indicate a large variability of the absorption for pollution particles. This variability strongly influences their direct radiative effect, with possible consequences on the hydrological cycle in this part of the basin.
Hélène Angot, Iris Dion, Nicolas Vogel, Michel Legrand, Olivier Magand, and Aurélien Dommergue
Atmos. Chem. Phys., 16, 8265–8279, https://doi.org/10.5194/acp-16-8265-2016, https://doi.org/10.5194/acp-16-8265-2016, 2016
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This paper presents a multi-year record of atmospheric gaseous elemental mercury (Hg(0)) at Dumont d’Urville (DDU) on the East Antarctic coast. This record reveals particularities that are not seen at other coastal Antarctic sites, likely due to the more frequent arrival of inland air masses at DDU than at other coastal sites, and to the influence of oceanic air masses. This study confirms the influence of processes observed inland on the cycle of atmospheric mercury at a continental scale.
Michel Legrand, Susanne Preunkert, Joël Savarino, Markus M. Frey, Alexandre Kukui, Detlev Helmig, Bruno Jourdain, Anna E. Jones, Rolf Weller, Neil Brough, and Hubert Gallée
Atmos. Chem. Phys., 16, 8053–8069, https://doi.org/10.5194/acp-16-8053-2016, https://doi.org/10.5194/acp-16-8053-2016, 2016
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Surface ozone, the most abundant atmospheric oxidant, has been measured since 2004 at the coastal East Antarctic site of Dumont d’Urville, and since 2007 at the Concordia station located on the high East Antarctic plateau. Long-term changes, seasonal and diurnal cycles, as well as inter-annual summer variability observed at these two East Antarctic sites are discussed. Influences like sea ice extent and outflow from inland Antarctica are discussed.
Gerard Ancellet, Jacques Pelon, Julien Totems, Patrick Chazette, Ariane Bazureau, Michaël Sicard, Tatiana Di Iorio, Francois Dulac, and Marc Mallet
Atmos. Chem. Phys., 16, 4725–4742, https://doi.org/10.5194/acp-16-4725-2016, https://doi.org/10.5194/acp-16-4725-2016, 2016
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A multi-lidar analysis conducted in the Mediterranean basin compares the impact of the long-range transport of North American biomass burning aerosols with the role of frequently observed Saharan dust outbreaks. This paper provides a detailed analysis of the potential North American aerosol sources, their transport to Europe and the mixing of different aerosol sources, using simulations of a particle dispersion model and lidar measurements of the aerosol optical properties.
Antoine Berchet, Philippe Bousquet, Isabelle Pison, Robin Locatelli, Frédéric Chevallier, Jean-Daniel Paris, Ed J. Dlugokencky, Tuomas Laurila, Juha Hatakka, Yrjo Viisanen, Doug E. J. Worthy, Euan Nisbet, Rebecca Fisher, James France, David Lowry, Viktor Ivakhov, and Ove Hermansen
Atmos. Chem. Phys., 16, 4147–4157, https://doi.org/10.5194/acp-16-4147-2016, https://doi.org/10.5194/acp-16-4147-2016, 2016
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We propose insights based on atmospheric observations around the Arctic circle to evaluate estimates of methane emissions to the atmosphere from the East Siberian Arctic Shelf. Based on a comprehensive statistical analysis of the observations and of high-resolution transport simulations, annual methane emissions from ESAS are estimated to range from 0.0 to 4.5 TgCH4 yr−1, with a maximum in summer and very low emissions in winter.
Patrick Chazette, Julien Totems, Gérard Ancellet, Jacques Pelon, and Michaël Sicard
Atmos. Chem. Phys., 16, 2863–2875, https://doi.org/10.5194/acp-16-2863-2016, https://doi.org/10.5194/acp-16-2863-2016, 2016
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We performed synergetic active and passive remote-sensing observations at Minorca (Spain), over more than 3 weeks in spring 2013. We characterized the aerosol optical properties and type using a combination of Rayleigh–Mie–Raman lidar and sun-photometer data. Results show a high variability due to changing atmospheric transport regimes and aerosol sources. Such variability significantly influences the radiative balance through the entire atmosphere and then the climate of the Mediterranean area.
Joël Savarino, William C. Vicars, Michel Legrand, Suzanne Preunkert, Bruno Jourdain, Markus M. Frey, Alexandre Kukui, Nicolas Caillon, and Jaime Gil Roca
Atmos. Chem. Phys., 16, 2659–2673, https://doi.org/10.5194/acp-16-2659-2016, https://doi.org/10.5194/acp-16-2659-2016, 2016
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Atmospheric nitrate is collected on the East Antarctic ice sheet. Nitrogen and oxygen stable isotopes and concentrations of nitrate are measured. Using a box model, we show that there is s systematic discrepancy between observations and model results. We suggest that this discrepancy probably results from unknown NOx chemistry above the Antarctic ice sheet. However, possible misconception in the stable isotope mass balance is not completely excluded.
N. Zannoni, V. Gros, M. Lanza, R. Sarda, B. Bonsang, C. Kalogridis, S. Preunkert, M. Legrand, C. Jambert, C. Boissard, and J. Lathiere
Atmos. Chem. Phys., 16, 1619–1636, https://doi.org/10.5194/acp-16-1619-2016, https://doi.org/10.5194/acp-16-1619-2016, 2016
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Our manuscript shows results of OH reactivity and Biogenic Volatile Organic Compounds (BVOCs) concentration during a field experiment conducted in late spring 2014 at the Observatoire de Haute Provence (OHP) site. We found that OH reactivity is among the highest measured in forests globally (69 s−1) and it is mainly due to isoprene. No missing reactivity was present during daytime inside or above the canopy, while 50 % missing reactivity was found by night at both heights.
M. L. Lamare, J. Lee-Taylor, and M. D. King
Atmos. Chem. Phys., 16, 843–860, https://doi.org/10.5194/acp-16-843-2016, https://doi.org/10.5194/acp-16-843-2016, 2016
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The decrease in reflectivity (albedo) of sea ice and snow containing mineral dusts and volcanic ashes is calculated. The type of snow and sea ice, the thickness and the layering of mineral aerosol deposits are varied. The results show that the response of the albedo of snow and sea ice to mineral aerosol deposits is more sensitive to the type of snow or sea ice than to the properties of the mineral aerosol deposits themselves.
M. Mallet, F. Dulac, P. Formenti, P. Nabat, J. Sciare, G. Roberts, J. Pelon, G. Ancellet, D. Tanré, F. Parol, C. Denjean, G. Brogniez, A. di Sarra, L. Alados-Arboledas, J. Arndt, F. Auriol, L. Blarel, T. Bourrianne, P. Chazette, S. Chevaillier, M. Claeys, B. D'Anna, Y. Derimian, K. Desboeufs, T. Di Iorio, J.-F. Doussin, P. Durand, A. Féron, E. Freney, C. Gaimoz, P. Goloub, J. L. Gómez-Amo, M. J. Granados-Muñoz, N. Grand, E. Hamonou, I. Jankowiak, M. Jeannot, J.-F. Léon, M. Maillé, S. Mailler, D. Meloni, L. Menut, G. Momboisse, J. Nicolas, T. Podvin, V. Pont, G. Rea, J.-B. Renard, L. Roblou, K. Schepanski, A. Schwarzenboeck, K. Sellegri, M. Sicard, F. Solmon, S. Somot, B Torres, J. Totems, S. Triquet, N. Verdier, C. Verwaerde, F. Waquet, J. Wenger, and P. Zapf
Atmos. Chem. Phys., 16, 455–504, https://doi.org/10.5194/acp-16-455-2016, https://doi.org/10.5194/acp-16-455-2016, 2016
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The aim of this article is to present an experimental campaign over the Mediterranean focused on aerosol-radiation measurements and modeling. Results indicate an important atmospheric loading associated with a moderate absorbing ability of mineral dust. Observations suggest a complex vertical structure and size distributions characterized by large aerosols within dust plumes. The radiative effect is highly variable, with negative forcing over the Mediterranean and positive over northern Africa.
V. Mikhalenko, S. Sokratov, S. Kutuzov, P. Ginot, M. Legrand, S. Preunkert, I. Lavrentiev, A. Kozachek, A. Ekaykin, X. Faïn, S. Lim, U. Schotterer, V. Lipenkov, and P. Toropov
The Cryosphere, 9, 2253–2270, https://doi.org/10.5194/tc-9-2253-2015, https://doi.org/10.5194/tc-9-2253-2015, 2015
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For the first time an ice core unaffected by melting was recovered from the western Elbrus plateau in the Caucasus. The preserved chemical and isotopic data are considered a source of paleo-climate information for southern/eastern Europe. Considerable snow accumulation (about 1500mm w.e.) and high sampling resolution allowed seasonal variability to be obtained in climate signals, covering a time period of about 200 years. Ice flow models suggest that the basal ice age can be more than 600 years.
J. Erbland, J. Savarino, S. Morin, J. L. France, M. M. Frey, and M. D. King
Atmos. Chem. Phys., 15, 12079–12113, https://doi.org/10.5194/acp-15-12079-2015, https://doi.org/10.5194/acp-15-12079-2015, 2015
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In this paper, we describe the development of a numerical model which aims at representing nitrate recycling at the air-snow interface on the East Antarctic Plateau. Stable isotopes are used as diagnostic and evaluation tools by comparing the model's results to recent field measurements of nitrate and key atmospheric species at Dome C, Antarctica. From sensitivity tests conducted with the model, we propose a framework for the interpretation of the nitrate isotope record in deep ice cores.
T. A. Berhanu, J. Savarino, J. Erbland, W. C. Vicars, S. Preunkert, J. F. Martins, and M. S. Johnson
Atmos. Chem. Phys., 15, 11243–11256, https://doi.org/10.5194/acp-15-11243-2015, https://doi.org/10.5194/acp-15-11243-2015, 2015
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In this field study at Dome C, Antarctica, we investigated the effect of solar UV photolysis on the stable isotopes of nitrate in snow via comparison of two identical snow pits while exposing only one to solar UV. From the difference between the average isotopic fractionations calculated for each pit, we determined a purely photolytic nitrogen isotopic fractionation of -55.8‰, in good agreement with what has been recently determined in a laboratory study.
C. Di Biagio, L. Doppler, C. Gaimoz, N. Grand, G. Ancellet, J.-C. Raut, M. Beekmann, A. Borbon, K. Sartelet, J.-L. Attié, F. Ravetta, and P. Formenti
Atmos. Chem. Phys., 15, 9611–9630, https://doi.org/10.5194/acp-15-9611-2015, https://doi.org/10.5194/acp-15-9611-2015, 2015
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Observations from this study indicate that continental pollution largely affects the atmospheric composition and structure of the western Mediterranean basin. Pollution plumes reach 3000-4000 m in altitude and present a very complex and highly stratified structure, characterized by fresh and aged layers both in the boundary layer and in the free troposphere. Also we report the observations of high levels of ultrafine particles over the basin, possibly linked to new particle formation events.
M. M. Frey, H. K. Roscoe, A. Kukui, J. Savarino, J. L. France, M. D. King, M. Legrand, and S. Preunkert
Atmos. Chem. Phys., 15, 7859–7875, https://doi.org/10.5194/acp-15-7859-2015, https://doi.org/10.5194/acp-15-7859-2015, 2015
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Surprisingly large concentrations and flux of atmospheric nitrogen oxides were measured at Dome C, East Antarctica. It was found that the surface snow holds a significant reservoir of photochemically produced NOx and is a sink of gas-phase ozone. Main drivers of NOx snow emissions were large snow nitrate concentrations, with contributions of increased UV from decreases in stratospheric ozone. Observed halogen and hydroxyl radical concentrations were too low to explain large NO2:NO ratios.
H. G. Chan, M. D. King, and M. M. Frey
Atmos. Chem. Phys., 15, 7913–7927, https://doi.org/10.5194/acp-15-7913-2015, https://doi.org/10.5194/acp-15-7913-2015, 2015
S. Preunkert, M. Legrand, M. M. Frey, A. Kukui, J. Savarino, H. Gallée, M. King, B. Jourdain, W. Vicars, and D. Helmig
Atmos. Chem. Phys., 15, 6689–6705, https://doi.org/10.5194/acp-15-6689-2015, https://doi.org/10.5194/acp-15-6689-2015, 2015
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During two austral summers HCHO was investigated in air, snow, and interstitial air at the Concordia site located on the East Antarctic Plateau. Snow emission fluxes were estimated to be around 1 to 2 and 3 to 5 x 10^12 molecules m-2 s-1 at night and at noon, respectively. Shading experiments suggest that the photochemical HCHO production in the snowpack at Concordia remains negligible. The mean HCHO level of 130pptv observed at 1m above the surface is quite well reproduced by 1-D simulations.
H. Gallée, S. Preunkert, S. Argentini, M. M. Frey, C. Genthon, B. Jourdain, I. Pietroni, G. Casasanta, H. Barral, E. Vignon, C. Amory, and M. Legrand
Atmos. Chem. Phys., 15, 6225–6236, https://doi.org/10.5194/acp-15-6225-2015, https://doi.org/10.5194/acp-15-6225-2015, 2015
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Regional climate model MAR was run for the region of Dome C located on the East Antarctic plateau, during summer 2011–2012, with a high vertical resolution in the lower troposphere. MAR is generally in very good agreement with the observations and provides sufficiently reliable information about surface turbulent fluxes and vertical profiles of vertical diffusion coefficients when discussing the representativeness of chemical measurements made nearby the ground surface at Dome C.
L. Marelle, J.-C. Raut, J. L. Thomas, K. S. Law, B. Quennehen, G. Ancellet, J. Pelon, A. Schwarzenboeck, and J. D. Fast
Atmos. Chem. Phys., 15, 3831–3850, https://doi.org/10.5194/acp-15-3831-2015, https://doi.org/10.5194/acp-15-3831-2015, 2015
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.
S. J. O'Shea, G. Allen, M. W. Gallagher, K. Bower, S. M. Illingworth, J. B. A. Muller, B. T. Jones, C. J. Percival, S. J-B. Bauguitte, M. Cain, N. Warwick, A. Quiquet, U. Skiba, J. Drewer, K. Dinsmore, E. G. Nisbet, D. Lowry, R. E. Fisher, J. L. France, M. Aurela, A. Lohila, G. Hayman, C. George, D. B. Clark, A. J. Manning, A. D. Friend, and J. Pyle
Atmos. Chem. Phys., 14, 13159–13174, https://doi.org/10.5194/acp-14-13159-2014, https://doi.org/10.5194/acp-14-13159-2014, 2014
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This paper presents airborne measurements of greenhouse gases collected in the European Arctic. Regional scale flux estimates for the northern Scandinavian wetlands are derived. These fluxes are found to be in excellent agreement with coincident surface measurements within the aircraft's sampling domain. This has allowed a significant low bias to be identified in two commonly used process-based land surface models.
M. Legrand, S. Preunkert, M. Frey, Th. Bartels-Rausch, A. Kukui, M. D. King, J. Savarino, M. Kerbrat, and B. Jourdain
Atmos. Chem. Phys., 14, 9963–9976, https://doi.org/10.5194/acp-14-9963-2014, https://doi.org/10.5194/acp-14-9963-2014, 2014
A. A. Marks and M. D. King
The Cryosphere, 8, 1625–1638, https://doi.org/10.5194/tc-8-1625-2014, https://doi.org/10.5194/tc-8-1625-2014, 2014
G. Ancellet, J. Pelon, Y. Blanchard, B. Quennehen, A. Bazureau, K. S. Law, and A. Schwarzenboeck
Atmos. Chem. Phys., 14, 8235–8254, https://doi.org/10.5194/acp-14-8235-2014, https://doi.org/10.5194/acp-14-8235-2014, 2014
X. Faïn, J. Chappellaz, R. H. Rhodes, C. Stowasser, T. Blunier, J. R. McConnell, E. J. Brook, S. Preunkert, M. Legrand, T. Debois, and D. Romanini
Clim. Past, 10, 987–1000, https://doi.org/10.5194/cp-10-987-2014, https://doi.org/10.5194/cp-10-987-2014, 2014
C. Jouan, J. Pelon, E. Girard, G. Ancellet, J. P. Blanchet, and J. Delanoë
Atmos. Chem. Phys., 14, 1205–1224, https://doi.org/10.5194/acp-14-1205-2014, https://doi.org/10.5194/acp-14-1205-2014, 2014
Q. Libois, G. Picard, J. L. France, L. Arnaud, M. Dumont, C. M. Carmagnola, and M. D. King
The Cryosphere, 7, 1803–1818, https://doi.org/10.5194/tc-7-1803-2013, https://doi.org/10.5194/tc-7-1803-2013, 2013
P. J. Nair, S. Godin-Beekmann, J. Kuttippurath, G. Ancellet, F. Goutail, A. Pazmiño, L. Froidevaux, J. M. Zawodny, R. D. Evans, H. J. Wang, J. Anderson, and M. Pastel
Atmos. Chem. Phys., 13, 10373–10384, https://doi.org/10.5194/acp-13-10373-2013, https://doi.org/10.5194/acp-13-10373-2013, 2013
M. Legrand, S. Preunkert, B. Jourdain, J. Guilhermet, X. Fa{ï}n, I. Alekhina, and J. R. Petit
Clim. Past, 9, 2195–2211, https://doi.org/10.5194/cp-9-2195-2013, https://doi.org/10.5194/cp-9-2195-2013, 2013
S. Masclin, M. M. Frey, W. F. Rogge, and R. C. Bales
Atmos. Chem. Phys., 13, 8857–8877, https://doi.org/10.5194/acp-13-8857-2013, https://doi.org/10.5194/acp-13-8857-2013, 2013
A. A. Marks and M. D. King
The Cryosphere, 7, 1193–1204, https://doi.org/10.5194/tc-7-1193-2013, https://doi.org/10.5194/tc-7-1193-2013, 2013
J. Erbland, W. C. Vicars, J. Savarino, S. Morin, M. M. Frey, D. Frosini, E. Vince, and J. M. F. Martins
Atmos. Chem. Phys., 13, 6403–6419, https://doi.org/10.5194/acp-13-6403-2013, https://doi.org/10.5194/acp-13-6403-2013, 2013
S. Preunkert and M. Legrand
Clim. Past, 9, 1403–1416, https://doi.org/10.5194/cp-9-1403-2013, https://doi.org/10.5194/cp-9-1403-2013, 2013
J. L. Thomas, J.-C. Raut, K. S. Law, L. Marelle, G. Ancellet, F. Ravetta, J. D. Fast, G. Pfister, L. K. Emmons, G. S. Diskin, A. Weinheimer, A. Roiger, and H. Schlager
Atmos. Chem. Phys., 13, 3825–3848, https://doi.org/10.5194/acp-13-3825-2013, https://doi.org/10.5194/acp-13-3825-2013, 2013
M. M. Frey, N. Brough, J. L. France, P. S. Anderson, O. Traulle, M. D. King, A. E. Jones, E. W. Wolff, and J. Savarino
Atmos. Chem. Phys., 13, 3045–3062, https://doi.org/10.5194/acp-13-3045-2013, https://doi.org/10.5194/acp-13-3045-2013, 2013
Related subject area
Subject: Gases | Research Activity: Field Measurements | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Observation and modeling of atmospheric OH and HO2∗ radicals at a subtropical rural site and implications for secondary pollutants
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Isotopic signatures of methane emission from oil and natural gas plants in southwestern China
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Characterization of nitrous acid and its potential effects on secondary pollution in the warm season in Beijing urban areas
Vertical changes in volatile organic compounds (VOCs) and impacts on photochemical ozone formation
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Atmospheric carbonyl compounds are crucial in regional ozone heavy pollution: insights from the Chengdu Plain Urban Agglomeration, China
Evaluating urban methane emissions and their attributes in a megacity, Osaka, Japan, via mobile and eddy covariance measurements
Ozone (O3) observations in Saxony, Germany for 1997–2020: Trends, modelling and implications for O3 control
Understanding summertime peroxyacetyl nitrate (PAN) formation and its relation to aerosol pollution: insights from high-resolution measurements and modeling
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Seasonal air concentration variability, gas–particle partitioning, precipitation scavenging, and air–water equilibrium of organophosphate esters in southern Canada
Measurement report: Surface exchange fluxes of HONO during the growth process of paddy fields in the Huaihe River Basin, China
Hemispheric differences in ozone across the stratosphere-troposphere exchange region
Molecular and seasonal characteristics of organic vapors in urban Beijing: insights from Vocus-PTR measurements
BVOC and speciated monoterpene concentrations and fluxes at a Scandinavian boreal forest
The variations in volatile organic compounds based on the policy change for Omicron in the traffic hub of Zhengzhou
On the dynamics of ozone depletion events at Villum Research Station in the High Arctic
Measurement report: Long-term measurements of surface ozone and trends in semi-natural sub-Saharan African ecosystems
Characterization of biogenic volatile organic compounds and their oxidation products in a stressed spruce-dominated forest close to a biogas power plant
Reactive chlorine-, sulfur-, and nitrogen-containing volatile organic compounds impact atmospheric chemistry in the megacity of Delhi during both clean and extremely polluted seasons
Analysis of the day-to-day variability of ozone vertical profiles in the lower troposphere during the 2022 Paris ACROSS campaign
Ozone deposition measurements over wheat fields in the North China Plain: variability and related factors of deposition flux and velocity
Consistency evaluation of tropospheric ozone from ozonesonde and IAGOS (In-service Aircraft for a Global Observing System) observations: vertical distribution, ozonesonde types, and station–airport distance
CO2 and CO temporal variability over Mexico City from ground-based total column and surface measurements
Investigating carbonyl compounds above the Amazon rainforest using a proton-transfer-reaction time-of-flight mass spectrometer (PTR-ToF-MS) with NO+ chemical ionization
Measurement report: In-flight and ground-based measurements of nitrogen oxide emissions from latest-generation jet engines and 100 % sustainable aviation fuel
Measurement report: Sources, sinks, and lifetime of NOx in a suburban temperate forest at night
Measurement report: Urban ammonia and amines in Houston, Texas
Biomass-burning sources control ambient particulate matter, but traffic and industrial sources control volatile organic compound (VOC) emissions and secondary-pollutant formation during extreme pollution events in Delhi
Multi-year observations of variable incomplete combustion in the New York megacity
Observations of the vertical distributions of summertime atmospheric pollutants in Nam Co: OH production and source analysis
Zhouxing Zou, Tianshu Chen, Qianjie Chen, Weihang Sun, Shichun Han, Zhuoyue Ren, Xinyi Li, Wei Song, Aoqi Ge, Qi Wang, Xiao Tian, Chenglei Pei, Xinming Wang, Yanli Zhang, and Tao Wang
Atmos. Chem. Phys., 25, 8147–8161, https://doi.org/10.5194/acp-25-8147-2025, https://doi.org/10.5194/acp-25-8147-2025, 2025
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We measured ambient OH and HO2* (HO2 and contribution from RO2, organic peroxyl radicals) concentrations at a subtropical rural site and compared our observations with model results. During warm periods, the model overestimated concentrations of OH and HO2, leading to overestimation of ozone and nitric acid production. Our findings highlight the need to better understand how OH and HO2 are formed and removed, which is important for accurate air quality and climate predictions.
Markus Jesswein, Valentin Lauther, Nicolas Emig, Peter Hoor, Timo Keber, Hans-Christoph Lachnitt, Linda Ort, Tanja Schuck, Johannes Strobel, Ronja Van Luijt, C. Michael Volk, Franziska Weyland, and Andreas Engel
Atmos. Chem. Phys., 25, 8107–8126, https://doi.org/10.5194/acp-25-8107-2025, https://doi.org/10.5194/acp-25-8107-2025, 2025
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The study investigates transport within the Asian Summer Monsoon, focusing on how CH2Cl2 reaches the subarctic tropopause region. Using data from the PHILEAS campaign in 2023, events with increased mixing ratios were detected. Their origin, the transport paths to the tropopause region, and the potential entry into the stratosphere were analyzed. The East Asian Summer Monsoon was identified as the main transport pathway, with only a small contribution to the stratosphere in the following days.
Yanjie Lu, Xinxin Feng, Yanli Feng, Minjun Jiang, Yu Peng, Tian Chen, and Yingjun Chen
Atmos. Chem. Phys., 25, 8043–8059, https://doi.org/10.5194/acp-25-8043-2025, https://doi.org/10.5194/acp-25-8043-2025, 2025
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Through lab tests and field measurements from typical sources, we found that carbonyl compounds from biomass burning are an order of magnitude higher than those from vehicles. The formation of carbonyl compounds in solid and liquid fuel is governed by combustion temperature and emission standards, respectively. Fuel type determines the chemical composition. Biomass burning and farm machinery are key drivers of atmospheric oxidation capacity. This study provides actionable solutions to safeguard public health.
Gaojie Chen, Xiaolong Fan, Haichao Wang, Yee Jun Tham, Ziyi Lin, Xiaoting Ji, Lingling Xu, Baoye Hu, and Jinsheng Chen
Atmos. Chem. Phys., 25, 7815–7828, https://doi.org/10.5194/acp-25-7815-2025, https://doi.org/10.5194/acp-25-7815-2025, 2025
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Our study revealed that the nighttime heterogeneous dinitrogen pentoxide (N2O5) uptake process was the major contributor of nitryl chloride (ClNO2) sources, while nitrate photolysis may promote the elevation of daytime ClNO2 concentrations. The rates of alkane oxidation by chlorine (Cl) radical in the early morning exceeded those by OH radical, significantly promoted the formation of ROx and ozone (O3), and further enhanced the atmospheric oxidation capacity levels.
Jingwen Dai, Kun Zhang, Yanli Feng, Xin Yi, Rui Li, Jin Xue, Qing Li, Lishu Shi, Jiaqiang Liao, Yanan Yi, Fangting Wang, Liumei Yang, Hui Chen, Ling Huang, Jiani Tan, Yangjun Wang, and Li Li
Atmos. Chem. Phys., 25, 7467–7484, https://doi.org/10.5194/acp-25-7467-2025, https://doi.org/10.5194/acp-25-7467-2025, 2025
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Oxygenated volatile organic compounds (OVOCs) are important ozone (O3) precursors. However, most O3 formation analysis based on the box model (OBM) does not include any OVOC constraint. To access the interference of OVOCs with O3 simulation, this study presents results from a field campaign and OBM analysis. Our results indicate that no OVOC constraint in the OBM can lead to overestimation of OVOCs, free radicals, and O3.
Roeland Van Malderen, Anne M. Thompson, Debra E. Kollonige, Ryan M. Stauffer, Herman G. J. Smit, Eliane Maillard Barras, Corinne Vigouroux, Irina Petropavlovskikh, Thierry Leblanc, Valérie Thouret, Pawel Wolff, Peter Effertz, David W. Tarasick, Deniz Poyraz, Gérard Ancellet, Marie-Renée De Backer, Stéphanie Evan, Victoria Flood, Matthias M. Frey, James W. Hannigan, José L. Hernandez, Marco Iarlori, Bryan J. Johnson, Nicholas Jones, Rigel Kivi, Emmanuel Mahieu, Glen McConville, Katrin Müller, Tomoo Nagahama, Justus Notholt, Ankie Piters, Natalia Prats, Richard Querel, Dan Smale, Wolfgang Steinbrecht, Kimberly Strong, and Ralf Sussmann
Atmos. Chem. Phys., 25, 7187–7225, https://doi.org/10.5194/acp-25-7187-2025, https://doi.org/10.5194/acp-25-7187-2025, 2025
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Tropospheric ozone is an important greenhouse gas and is an air pollutant. The time variability of tropospheric ozone is mainly driven by anthropogenic emissions. In this paper, we study the distribution and time variability of ozone from harmonized ground-based observations from five different measurement techniques. Our findings provide clear standard references for atmospheric models and evolving tropospheric ozone satellite data for the 2000–2022 period.
Can Ye, Pengfei Liu, Chaoyang Xue, Chenglong Zhang, Zhuobiao Ma, Chengtang Liu, Junfeng Liu, Keding Lu, Yujing Mu, and Yuanhang Zhang
Atmos. Chem. Phys., 25, 6991–7005, https://doi.org/10.5194/acp-25-6991-2025, https://doi.org/10.5194/acp-25-6991-2025, 2025
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This study investigates H2O2 chemistry in rural North China. The observed H2O2 showed distinct diurnal variations influenced by photochemical reactions. A box model revealed that H2O2 is primarily produced by HO2 recombination and removed mainly via particle uptake. Reductions in NOx, PM2.5, and alkanes raised H2O2 levels, while cutting alkenes, aromatics, CO, and HONO lowered them. A dual strategy focusing on VOC and NOx control is essential to reduce both H2O2 and ozone pollution.
Marvin Dufresne, Thérèse Salameh, Thierry Leonardis, Grégory Gille, Alexandre Armengaud, and Stéphane Sauvage
Atmos. Chem. Phys., 25, 5977–5999, https://doi.org/10.5194/acp-25-5977-2025, https://doi.org/10.5194/acp-25-5977-2025, 2025
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This paper discusses the 18-month-long measurement of non-methane hydrocarbons (NMHCs) in Marseille, where there was no measurement since early 2000, despite the impact of NMHCs on air quality and climate. Traffic-related sources are the largest contributor to NMHC concentrations in Marseille, and shipping strongly contributes to the formation of aerosols. Finally, the Covid-19 lockdown had an impact on NMHC concentrations, reaching a 50 % decrease for traffic-related sources.
Simone T. Andersen, Rolf Sander, Patrick Dewald, Laura Wüst, Tobias Seubert, Gunther N. T. E. Türk, Jan Schuladen, Max R. McGillen, Chaoyang Xue, Abdelwahid Mellouki, Alexandre Kukui, Vincent Michoud, Manuela Cirtog, Mathieu Cazaunau, Astrid Bauville, Hichem Bouzidi, Paola Formenti, Cyrielle Denjean, Jean-Claude Etienne, Olivier Garrouste, Christopher Cantrell, Jos Lelieveld, and John N. Crowley
Atmos. Chem. Phys., 25, 5893–5909, https://doi.org/10.5194/acp-25-5893-2025, https://doi.org/10.5194/acp-25-5893-2025, 2025
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Measurements and modelling of reactive nitrogen gases observed in a suburban temperate forest in Rambouillet, France, circa 50 km southwest of Paris in 2022 indicate that the biosphere rapidly scavenges organic nitrates of mixed biogenic and anthropogenic origin, resulting in short lifetimes for, for example, alkyl nitrates and peroxy nitrates.
Pengfei Han, Ning Zeng, Bo Yao, Wen Zhang, Weijun Quan, Pucai Wang, Ting Wang, Minqiang Zhou, Qixiang Cai, Yuzhong Zhang, Ruosi Liang, Wanqi Sun, and Shengxiang Liu
Atmos. Chem. Phys., 25, 4965–4988, https://doi.org/10.5194/acp-25-4965-2025, https://doi.org/10.5194/acp-25-4965-2025, 2025
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Methane (CH4) is a potent greenhouse gas. Northern China contributes a large proportion of CH4 emissions, yet large observation gaps exist. Here we compiled a comprehensive dataset, which is publicly available, that includes ground-based, satellite-based, inventory, and modeling results to show the CH4 concentrations, enhancements, and spatial–temporal variations. The data can benefit the research community and policy-makers for future observations, atmospheric inversions, and policy-making.
Timur Cinay, Dickon Young, Nazaret Narváez Jimenez, Cristina Vintimilla-Palacios, Ariel Pila Alonso, Paul B. Krummel, William Vizuete, and Andrew R. Babbin
Atmos. Chem. Phys., 25, 4703–4718, https://doi.org/10.5194/acp-25-4703-2025, https://doi.org/10.5194/acp-25-4703-2025, 2025
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We present the initial 15 months of nitrous oxide measurements from the Galapagos Emissions Monitoring Station. The observed variability in atmospheric mole fractions during this period can be linked to several factors: seasonal variations in trade wind speed and direction across the eastern Pacific, differences in the transport history of air masses sampled, and spatiotemporal heterogeneity in regional marine nitrous oxide emissions from the coastal upwelling systems of Peru and Chile.
Petra Bauerová, Josef Keder, Adriana Šindelářová, Ondřej Vlček, William Patiño, Pavel Krč, Jan Geletič, Hynek Řezníček, Martin Bureš, Kryštof Eben, Michal Belda, Jelena Radović, Vladimír Fuka, Radek Jareš, Igor Esau, and Jaroslav Resler
Atmos. Chem. Phys., 25, 4477–4504, https://doi.org/10.5194/acp-25-4477-2025, https://doi.org/10.5194/acp-25-4477-2025, 2025
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The study explored urban air quality in Prague using low-cost sensors and highlighted the multivariate adaptive regression splines (MARS) correction method's effectiveness in enhancing accuracy. Results showed traffic's impact on nitrogen dioxide levels and atmospheric dynamics on particulate matter. The research confirmed MARS-corrected sensors as cost-effective for monitoring, despite challenges like sensor ageing and data quality control.
Chunmeng Li, Xiaorui Chen, Haichao Wang, Tianyu Zhai, Xuefei Ma, Xinping Yang, Shiyi Chen, Min Zhou, Shengrong Lou, Xin Li, Limin Zeng, and Keding Lu
Atmos. Chem. Phys., 25, 3905–3918, https://doi.org/10.5194/acp-25-3905-2025, https://doi.org/10.5194/acp-25-3905-2025, 2025
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This study reports an observation of organic nitrate (including total peroxy nitrates and total alkyl nitrates) in Shanghai, China, during the summer of 2021, by homemade thermal dissociation cavity-enhanced absorption spectroscopy (TD-CEAS; Atmos. Meas. Tech., 14, 4033–4051, 2021). The distribution of organic nitrates and their effects on local ozone production are analyzed based on field observations in conjunction with model simulations.
Xudong Zheng and Shaodong Xie
Atmos. Chem. Phys., 25, 3807–3820, https://doi.org/10.5194/acp-25-3807-2025, https://doi.org/10.5194/acp-25-3807-2025, 2025
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To reduce uncertainties in identifying the key volatile organic compounds (VOCs) in ozone (O3) formation from ambient concentrations, this study comprehensively calculates the emitted VOC concentrations during both nighttime and daytime using the nitrate radical, O3, and hydroxyl radical reaction rates and ambient VOC concentrations. Based on the emitted concentrations, isoprene is one of the top three species contributing to O3 formation, which may be overlooked in observed concentrations.
Sina Hasheminassab, David M. Tratt, Olga V. Kalashnikova, Clement S. Chang, Morad Alvarez, Kerry N. Buckland, Michael J. Garay, Francesca M. Hopkins, Eric R. Keim, Le Kuai, Yaning Miao, Payam Pakbin, William C. Porter, and Mohammad H. Sowlat
EGUsphere, https://doi.org/10.5194/egusphere-2025-1378, https://doi.org/10.5194/egusphere-2025-1378, 2025
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Ammonia (NH3) is a key air pollutant linked to fine particle pollution, yet its sources remain poorly understood. Using airborne infrared imaging and ground sensors, we mapped NH3 emissions in California’s Salton Sea region with unprecedented detail. We found high emissions from farms, geothermal plants, and waste sites, including sources missing from inventories. These findings highlight the need for better NH3 monitoring to improve air quality models and guide pollution reduction strategies.
Mingxue Li, Men Xia, Chunshui Lin, Yifan Jiang, Weihang Sun, Yurun Wang, Yingnan Zhang, Maoxia He, and Tao Wang
Atmos. Chem. Phys., 25, 3753–3764, https://doi.org/10.5194/acp-25-3753-2025, https://doi.org/10.5194/acp-25-3753-2025, 2025
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Our field campaigns observed a strong diel pattern of chloroacetic acid as well as a strong correlation between its level and that of reactive chlorine species at a coastal site. Using quantum chemical calculations and box model simulation with an updated Master Chemical Mechanism, we found that the formation pathway of chloroacetic acid involved multiphase processes. Our study enhances understanding of atmospheric organic chlorine chemistry and emphasizes the importance of multiphase reactions.
Renzhi Hu, Guoxian Zhang, Haotian Cai, Jingyi Guo, Keding Lu, Xin Li, Shengrong Lou, Zhaofeng Tan, Changjin Hu, Pinhua Xie, and Wenqing Liu
Atmos. Chem. Phys., 25, 3011–3028, https://doi.org/10.5194/acp-25-3011-2025, https://doi.org/10.5194/acp-25-3011-2025, 2025
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A full suite of radical measurements (OH, HO2, RO2, and kOH) was established to accurately elucidate the limitations of oxidation in a chemically complex atmosphere. Sensitivity tests revealed that the incorporation of complex processes enabled a balance in both radical concentrations and coordinate ratios, effectively addressing the deficiency in the ozone generation mechanism. The full-chain radical detection bridged the gap between the photochemistry and the intensive oxidation level.
Dingxi Chen, Yi Liu, Zetong Niu, Ao Wang, Pius Otwil, Yuanyuan Huang, Zhongcong Sun, Xiaobing Pang, Liyang Zhan, and Longfei Yu
EGUsphere, https://doi.org/10.5194/egusphere-2025-377, https://doi.org/10.5194/egusphere-2025-377, 2025
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We carried out studies at 11 oil and gas sites in Southwest China (an important natural gas production area), investigating the methane concentration distribution pattern and emission inventory of oil and gas industrial sites through a combination of ground monitoring and drone airborne monitoring techniques, and at the same time, utilizing stable isotope techniques to trace back the methane from the oil and gas sites.
Shuwen Guo, Xuan Zheng, Xiao He, Lewei Zeng, Liqiang He, Xian Wu, Yifei Dai, Zihao Huang, Ting Chen, Shupei Xiao, Yan You, Sheng Xiang, Shaojun Zhang, Jingkun Jiang, and Ye Wu
Atmos. Chem. Phys., 25, 2695–2705, https://doi.org/10.5194/acp-25-2695-2025, https://doi.org/10.5194/acp-25-2695-2025, 2025
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We considered two potential influencing factors of heavy-duty diesel vehicle emissions that are rarely mentioned in the literature: cumulative mileage and ambient temperatures. The results suggest that prolonged use of heavy-duty diesel vehicles and low ambient temperatures leads to reduced engine combustion efficiency, which in turn increases tailpipe emissions significantly.
Junling Li, Chaofan Lian, Mingyuan Liu, Hao Zhang, Yongxin Yan, Yufei Song, Chun Chen, Jiaqi Wang, Haijie Zhang, Yanqin Ren, Yucong Guo, Weigang Wang, Yisheng Xu, Hong Li, Jian Gao, and Maofa Ge
Atmos. Chem. Phys., 25, 2551–2568, https://doi.org/10.5194/acp-25-2551-2025, https://doi.org/10.5194/acp-25-2551-2025, 2025
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As a key source of hydroxyl (OH) radical, nitrous acid (HONO) has attracted much attention for its important role in the atmospheric oxidant capacity (AOC) increase. In this study, we made a comparison of the ambient levels, variation patterns, sources, and formation pathway in the warm season on the basis of continuous intensive observations at an urban site of Beijing. This work highlights the importance of HONO for the AOC in the warm season.
Xiao-Bing Li, Bin Yuan, Yibo Huangfu, Suxia Yang, Xin Song, Jipeng Qi, Xianjun He, Sihang Wang, Yubin Chen, Qing Yang, Yongxin Song, Yuwen Peng, Guiqian Tang, Jian Gao, Dasa Gu, and Min Shao
Atmos. Chem. Phys., 25, 2459–2472, https://doi.org/10.5194/acp-25-2459-2025, https://doi.org/10.5194/acp-25-2459-2025, 2025
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Online vertical gradient measurements of volatile organic compounds (VOCs), ozone, and NOx were conducted based on a 325 m tall tower in urban Beijing. Vertical changes in the concentrations, compositions, key drivers, and environmental impacts of VOCs were analyzed in this study. We find that VOC species display differentiated vertical variation patterns and distinct roles in contributing to photochemical ozone formation with increasing height in the urban planetary boundary layer.
Alina Fiehn, Maximilian Eckl, Magdalena Pühl, Tiziana Bräuer, Klaus-Dirk Gottschaldt, Heinfried Aufmhoff, Lisa Eirenschmalz, Gregor Neumann, Felicitas Sakellariou, Daniel Sauer, Robert Baumann, Guilherme De Aguiar Ventura, Winne Nayole Cadete, Dário Luciano Zua, Manuel Xavier, Paulo Correia, and Anke Roiger
EGUsphere, https://doi.org/10.5194/egusphere-2025-635, https://doi.org/10.5194/egusphere-2025-635, 2025
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In September 2022, the METHANE-To-Go Africa (MTGA) campaign, part of UNEP’s IMEO Methane Science Studies, conducted the first CH₄ emissions measurements from West Africa’s offshore oil and gas sector. Using an aircraft-based mass balance method, emissions from Angolan offshore facilities were quantified. Older, low-producing facilities showed higher emissions than newer ones. High-emission events were observed, highlighting the need for targeted monitoring and mitigation efforts.
Shigeyuki Ishidoya, Satoshi Sugawara, and Atsushi Okazaki
Atmos. Chem. Phys., 25, 1965–1987, https://doi.org/10.5194/acp-25-1965-2025, https://doi.org/10.5194/acp-25-1965-2025, 2025
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The 18O/16O ratio of atmospheric oxygen, δatm(18O), is higher than that of ocean water due to isotopic effects during biospheric activities. This is known as the Dole–Morita effect, and its millennial-scale variations are recorded in ice cores. However, small variations of δatm(18O) in the present day have never been detected so far. This paper presents the first observations of diurnal, seasonal, and secular variations in δatm(18O) and applies them to evaluate oxygen, carbon, and water cycles.
Delaney B. Kilgour, Christopher M. Jernigan, Olga Garmash, Sneha Aggarwal, Shengqian Zhou, Claudia Mohr, Matt E. Salter, Joel A. Thornton, Jian Wang, Paul Zieger, and Timothy H. Bertram
Atmos. Chem. Phys., 25, 1931–1947, https://doi.org/10.5194/acp-25-1931-2025, https://doi.org/10.5194/acp-25-1931-2025, 2025
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We report simultaneous measurements of dimethyl sulfide (DMS) and hydroperoxymethyl thioformate (HPMTF) in the eastern North Atlantic. We use an observationally constrained box model to show that cloud loss is the dominant sink of HPMTF in this region over 6 weeks, resulting in large reductions in DMS-derived products that contribute to aerosol formation and growth. Our findings indicate that fast cloud processing of HPMTF must be included in global models to accurately capture the sulfur cycle.
Jiemeng Bao, Xin Zhang, Zhenhai Wu, Li Zhou, Jun Qian, Qinwen Tan, Fumo Yang, Junhui Chen, Yunfeng Li, Hefan Liu, Liqun Deng, and Hong Li
Atmos. Chem. Phys., 25, 1899–1916, https://doi.org/10.5194/acp-25-1899-2025, https://doi.org/10.5194/acp-25-1899-2025, 2025
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We studied carbonyl compounds' role in ozone pollution in the Chengdu Plain Urban Agglomeration, China. During heavy pollution in August 2019, we measured carbonyls at nine sites and analyzed their impact. Areas with higher carbonyl levels, like Chengdu, had worse ozone pollution. While their abundance matters, chemical reactions with other pollutants are the main drivers. Our findings show regional cooperation is vital to reducing ozone pollution effectively.
Masahito Ueyama, Taku Umezawa, Yukio Terao, Mark Lunt, and James Lawrence France
EGUsphere, https://doi.org/10.5194/egusphere-2024-3926, https://doi.org/10.5194/egusphere-2024-3926, 2025
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Methane (CH4) emissions were measured in Megacity Osaka, Japan, using mobile and eddy covariance methods. The CH4 emissions were much higher than those reported in local inventories, with natural gas contributing up to 74 % of the emissions. Several CH4 sources not accounted for in current inventories were identified. These results emphasize the need for more comprehensive emissions tracking in urban areas to enhance climate change mitigation efforts.
Yaru Wang, Dominik van Pinxteren, Andreas Tilgner, Erik Hans Hoffmann, Max Hell, Susanne Bastian, and Hartmut Herrmann
EGUsphere, https://doi.org/10.5194/egusphere-2024-4202, https://doi.org/10.5194/egusphere-2024-4202, 2025
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Tropospheric ground-level ozone (O3) is a global air-quality pollutant and greenhouse gas. Long-term O3 trends from 16 stations in Saxony, Germany, were compared over three periods, revealing worsened O3 pollution over the last decade. O3 formation has been volatile organic compound (VOC)-limited at traffic and urban sites for the past 20 years. To mitigate O3 pollution, moderate nitrogen oxides and additional VOC controls, particularly in solvent use, should be prioritized in the coming years.
Baoye Hu, Naihua Chen, Rui Li, Mingqiang Huang, Jinsheng Chen, Youwei Hong, Lingling Xu, Xiaolong Fan, Mengren Li, Lei Tong, Qiuping Zheng, and Yuxiang Yang
Atmos. Chem. Phys., 25, 905–921, https://doi.org/10.5194/acp-25-905-2025, https://doi.org/10.5194/acp-25-905-2025, 2025
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Box modeling with the Master Chemical Mechanism (MCM) was used to explore summertime peroxyacetyl nitrate (PAN) formation and its link to aerosol pollution under high-ozone conditions. The MCM model is effective in the study of PAN photochemical formation and performed better during the clean period than the haze period. Machine learning analysis identified ammonia, nitrate, and fine particulate matter as the top three factors contributing to simulation bias.
Xiansheng Liu, Xun Zhang, Marvin Dufresne, Tao Wang, Lijie Wu, Rosa Lara, Roger Seco, Marta Monge, Ana Maria Yáñez-Serrano, Marie Gohy, Paul Petit, Audrey Chevalier, Marie-Pierre Vagnot, Yann Fortier, Alexia Baudic, Véronique Ghersi, Grégory Gille, Ludovic Lanzi, Valérie Gros, Leïla Simon, Heidi Héllen, Stefan Reimann, Zoé Le Bras, Michelle Jessy Müller, David Beddows, Siqi Hou, Zongbo Shi, Roy M. Harrison, William Bloss, James Dernie, Stéphane Sauvage, Philip K. Hopke, Xiaoli Duan, Taicheng An, Alastair C. Lewis, James R. Hopkins, Eleni Liakakou, Nikolaos Mihalopoulos, Xiaohu Zhang, Andrés Alastuey, Xavier Querol, and Thérèse Salameh
Atmos. Chem. Phys., 25, 625–638, https://doi.org/10.5194/acp-25-625-2025, https://doi.org/10.5194/acp-25-625-2025, 2025
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This study examines BTEX (benzene, toluene, ethylbenzene, xylenes) pollution in urban areas across seven European countries. Analyzing data from 22 monitoring sites, we found traffic and industrial activities significantly impact BTEX levels, with peaks during rush hours. The risk from BTEX exposure remains moderate, especially in high-traffic and industrial zones, highlighting the need for targeted air quality management to protect public health and improve urban air quality.
Yuening Li, Faqiang Zhan, Chubashini Shunthirasingham, Ying Duan Lei, Jenny Oh, Amina Ben Chaaben, Zhe Lu, Kelsey Lee, Frank A. P. C. Gobas, Hayley Hung, and Frank Wania
Atmos. Chem. Phys., 25, 459–472, https://doi.org/10.5194/acp-25-459-2025, https://doi.org/10.5194/acp-25-459-2025, 2025
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Organophosphate esters are important humanmade trace contaminants. Measuring them in the atmospheric gas phase, particles, precipitation, and surface water in Canada, we explore seasonal concentration variability, gas–particle partitioning, precipitation scavenging, and the air–water equilibrium. Whereas higher summer concentrations and efficient precipitation scavenging conform with expectations, the lack of a relationship between compound volatility and gas–particle partitioning is puzzling.
Fanhao Meng, Baobin Han, Min Qin, Wu Fang, Ke Tang, Dou Shao, Zhitang Liao, Jun Duan, Yan Feng, Yong Huang, Ting Ni, and Pinhua Xie
Atmos. Chem. Phys., 24, 14191–14208, https://doi.org/10.5194/acp-24-14191-2024, https://doi.org/10.5194/acp-24-14191-2024, 2024
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Comprehensive observations of HONO and NOx fluxes were conducted over paddy fields in the Huaihe River Basin. Consecutive peaks in HONO and NO fluxes suggest a potentially enhanced release of HONO and NO due to soil tillage, whereas waterlogged soil may inhibit microbial nitrification processes following irrigation. Notably, biological processes and light-driven NO2 reactions at the surface may serve as sources of HONO and influence the local HONO budget during rotary tillage.
Rodrigo J. Seguel, Charlie Opazo, Yann Cohen, Owen R. Cooper, Laura Gallardo, Björn-Martin Sinnhuber, Florian Obersteiner, Andreas Zahn, Peter Hoor, and Susanne Rohs
EGUsphere, https://doi.org/10.5194/egusphere-2024-3719, https://doi.org/10.5194/egusphere-2024-3719, 2024
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We explored differences in ozone levels between the Northern and Southern Hemispheres in the Stratosphere-troposphere exchange region. Using unique data from a research aircraft, we found significantly lower ozone levels (with stratospheric character) in the Southern Hemisphere, especially during years of severe ozone depletion. A Sudden Stratospheric Warming event in 2019 increased Southern Hemisphere ozone levels, highlighting the relationship between atmospheric events and ozone distribution.
Zhaojin An, Rujing Yin, Xinyan Zhao, Xiaoxiao Li, Yuyang Li, Yi Yuan, Junchen Guo, Yiqi Zhao, Xue Li, Dandan Li, Yaowei Li, Dongbin Wang, Chao Yan, Kebin He, Douglas R. Worsnop, Frank N. Keutsch, and Jingkun Jiang
Atmos. Chem. Phys., 24, 13793–13810, https://doi.org/10.5194/acp-24-13793-2024, https://doi.org/10.5194/acp-24-13793-2024, 2024
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Online Vocus-PTR measurements show the compositions and seasonal variations in organic vapors in urban Beijing. With enhanced sensitivity and mass resolution, various species at a level of sub-parts per trillion (ppt) and organics with multiple oxygens (≥ 3) were observed. The fast photooxidation process in summer leads to an increase in both concentration and proportion of organics with multiple oxygens, while, in other seasons, the variations in them could be influenced by mixed sources.
Ross Charles Petersen, Thomas Holst, Cheng Wu, Radovan Krejci, Jeremy Chan, Claudia Mohr, and Janne Rinne
EGUsphere, https://doi.org/10.5194/egusphere-2024-3410, https://doi.org/10.5194/egusphere-2024-3410, 2024
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Ecosystem-scale emissions of biogenic volatile organic compounds (BVOCs) are important for atmospheric chemistry. Here we investigate boreal BVOC fluxes from a forest in central Sweden. BVOC fluxes were measured above-canopy using proton-transfer-reaction mass spectrometry, while compound-specific monoterpene (MT) fluxes were assessed using a concentration gradient method. We also evaluate the impact of chemical degradation on observed sesquiterpene (SQT) and nighttime MT fluxes.
Bowen Zhang, Dong Zhang, Zhe Dong, Xinshuai Song, Ruiqin Zhang, and Xiao Li
Atmos. Chem. Phys., 24, 13587–13601, https://doi.org/10.5194/acp-24-13587-2024, https://doi.org/10.5194/acp-24-13587-2024, 2024
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To gain insight into the impact of changes due to epidemic control policies, we undertook continuous online monitoring of volatile organic compounds (VOCs) at an urban site in Zhengzhou over a 2-month period. This study examines the characteristics of VOCs, their sources, and their temporal evolution. It also assesses the impact of the policy change on VOC pollution during the monitoring period, thus providing a basis for further research on VOC pollution and source control.
Jakob Boyd Pernov, Jens Liengaard Hjorth, Lise Lotte Sørensen, and Henrik Skov
Atmos. Chem. Phys., 24, 13603–13631, https://doi.org/10.5194/acp-24-13603-2024, https://doi.org/10.5194/acp-24-13603-2024, 2024
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Arctic ozone depletion events (ODEs) occur every spring and have vast implications for the oxidizing capacity, radiative balance, and mercury oxidation. In this study, we analyze ozone, ODEs, and their connection to meteorological and air mass history variables through statistical analyses, back trajectories, and machine learning (ML) at Villum Research Station. ODEs are favorable under sunny, calm conditions with air masses arriving from northerly wind directions with sea ice contact.
Hagninou Elagnon Venance Donnou, Aristide Barthélémy Akpo, Money Ossohou, Claire Delon, Véronique Yoboué, Dungall Laouali, Marie Ouafo-Leumbe, Pieter Gideon Van Zyl, Ousmane Ndiaye, Eric Gardrat, Maria Dias-Alves, and Corinne Galy-Lacaux
Atmos. Chem. Phys., 24, 13151–13182, https://doi.org/10.5194/acp-24-13151-2024, https://doi.org/10.5194/acp-24-13151-2024, 2024
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Ozone is a secondary air pollutant that is detrimental to human and plant health. A better understanding of its chemical evolution is a challenge for Africa, where it is still undersampled. Out of 14 sites examined (1995–2020), high levels of O3 are reported in southern Africa. The dominant chemical processes leading to O3 formation are identified. A decrease in O3 is observed at Katibougou (Mali) and Banizoumbou (Niger), and an increase is found at Zoétélé (Cameroon) and Skukuza (South Africa).
Junwei Song, Georgios I. Gkatzelis, Ralf Tillmann, Nicolas Brüggemann, Thomas Leisner, and Harald Saathoff
Atmos. Chem. Phys., 24, 13199–13217, https://doi.org/10.5194/acp-24-13199-2024, https://doi.org/10.5194/acp-24-13199-2024, 2024
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Biogenic volatile organic compounds (BVOCs) and organic aerosol (OA) particles were measured online in a stressed spruce-dominated forest. OA was mainly attributed to the monoterpene oxidation products. The mixing ratios of BVOCs were higher than the values previously measured in other temperate forests. The results demonstrate that BVOCs are influenced not only by meteorology and biogenic emissions but also by local anthropogenic emissions and subsequent chemical transformation processes.
Sachin Mishra, Vinayak Sinha, Haseeb Hakkim, Arpit Awasthi, Sachin D. Ghude, Vijay Kumar Soni, Narendra Nigam, Baerbel Sinha, and Madhavan N. Rajeevan
Atmos. Chem. Phys., 24, 13129–13150, https://doi.org/10.5194/acp-24-13129-2024, https://doi.org/10.5194/acp-24-13129-2024, 2024
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We quantified 111 gases using mass spectrometry to understand how seasonal and emission changes lead from clean air in the monsoon season to extremely polluted air in the post-monsoon season in Delhi. Averaged total mass concentrations (260 µg m-3) were > 4 times in polluted periods, driven by biomass burning emissions and reduced atmospheric ventilation. Reactive gaseous nitrogen, chlorine, and sulfur compounds hitherto unreported from such a polluted environment were discovered.
Gérard Ancellet, Camille Viatte, Anne Boynard, François Ravetta, Jacques Pelon, Cristelle Cailteau-Fischbach, Pascal Genau, Julie Capo, Axel Roy, and Philippe Nédélec
Atmos. Chem. Phys., 24, 12963–12983, https://doi.org/10.5194/acp-24-12963-2024, https://doi.org/10.5194/acp-24-12963-2024, 2024
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Characterization of ozone pollution in urban areas benefited from a measurement campaign in summer 2022 in the Paris region. The analysis is based on 21 d of lidar and aircraft observations. The main objective is an analysis of the sensitivity of ozone pollution to the micrometeorological processes in the urban atmospheric boundary layer and the transport of regional pollution. The paper also discusses to what extent satellite observations can track observed ozone plumes.
Xiaoyi Zhang, Wanyun Xu, Weili Lin, Gen Zhang, Jinjian Geng, Li Zhou, Huarong Zhao, Sanxue Ren, Guangsheng Zhou, Jianmin Chen, and Xiaobin Xu
Atmos. Chem. Phys., 24, 12323–12340, https://doi.org/10.5194/acp-24-12323-2024, https://doi.org/10.5194/acp-24-12323-2024, 2024
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Ozone (O3) deposition is a key process that removes surface O3, affecting air quality, ecosystems and climate change. We conducted O3 deposition measurement over a wheat canopy using a newly relaxed eddy accumulation flux system. Large variabilities in O3 deposition were detected, mainly determined by crop growth and modulated by various environmental factors. More O3 deposition observations over different surfaces are needed for exploring deposition mechanisms and model optimization.
Honglei Wang, David W. Tarasick, Jane Liu, Herman G. J. Smit, Roeland Van Malderen, Lijuan Shen, Romain Blot, and Tianliang Zhao
Atmos. Chem. Phys., 24, 11927–11942, https://doi.org/10.5194/acp-24-11927-2024, https://doi.org/10.5194/acp-24-11927-2024, 2024
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In this study, we identify 23 suitable pairs of sites from World Ozone and Ultraviolet Radiation Data Centre (WOUDC) and In-service Aircraft for a Global Observing System (IAGOS) datasets (1995 to 2021), compare the average vertical distributions of tropospheric O3 from ozonesonde and aircraft measurements, and analyze the differences based on ozonesonde type and station–airport distance.
Noémie Taquet, Wolfgang Stremme, María Eugenia González del Castillo, Victor Almanza, Alejandro Bezanilla, Olivier Laurent, Carlos Alberti, Frank Hase, Michel Ramonet, Thomas Lauvaux, Ke Che, and Michel Grutter
Atmos. Chem. Phys., 24, 11823–11848, https://doi.org/10.5194/acp-24-11823-2024, https://doi.org/10.5194/acp-24-11823-2024, 2024
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We characterize the variability in CO and CO2 emissions over Mexico City from long-term time-resolved Fourier transform infrared spectroscopy solar absorption and surface measurements from 2013 to 2021. Using the average intraday CO growth rate from total columns, the average CO / CO2 ratio and TROPOMI data, we estimate the interannual variability in the CO and CO2 anthropogenic emissions of Mexico City, highlighting the effect of an unprecedented drop in activity due to the COVID-19 lockdown.
Akima Ringsdorf, Achim Edtbauer, Bruna Holanda, Christopher Poehlker, Marta O. Sá, Alessandro Araújo, Jürgen Kesselmeier, Jos Lelieveld, and Jonathan Williams
Atmos. Chem. Phys., 24, 11883–11910, https://doi.org/10.5194/acp-24-11883-2024, https://doi.org/10.5194/acp-24-11883-2024, 2024
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We show the average height distribution of separately observed aldehydes and ketones over a day and discuss their rainforest-specific sources and sinks as well as their seasonal changes above the Amazon. Ketones have much longer atmospheric lifetimes than aldehydes and thus different implications for atmospheric chemistry. However, they are commonly observed together, which we overcome by measuring with a NO+ chemical ionization mass spectrometer for the first time in the Amazon rainforest.
Theresa Harlass, Rebecca Dischl, Stefan Kaufmann, Raphael Märkl, Daniel Sauer, Monika Scheibe, Paul Stock, Tiziana Bräuer, Andreas Dörnbrack, Anke Roiger, Hans Schlager, Ulrich Schumann, Magdalena Pühl, Tobias Schripp, Tobias Grein, Linda Bondorf, Charles Renard, Maxime Gauthier, Mark Johnson, Darren Luff, Paul Madden, Peter Swann, Denise Ahrens, Reetu Sallinen, and Christiane Voigt
Atmos. Chem. Phys., 24, 11807–11822, https://doi.org/10.5194/acp-24-11807-2024, https://doi.org/10.5194/acp-24-11807-2024, 2024
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Emissions from aircraft have a direct impact on our climate. Here, we present airborne and ground-based measurement data of nitrogen oxides that were collected in the exhaust of an Airbus aircraft. We study the impact of burning fossil and sustainable aviation fuel on nitrogen oxide emissions at different engine settings related to combustor temperature, pressure and fuel flow. Further, we compare observations with engine emission models.
Simone T. Andersen, Max R. McGillen, Chaoyang Xue, Tobias Seubert, Patrick Dewald, Gunther N. T. E. Türk, Jan Schuladen, Cyrielle Denjean, Jean-Claude Etienne, Olivier Garrouste, Marina Jamar, Sergio Harb, Manuela Cirtog, Vincent Michoud, Mathieu Cazaunau, Antonin Bergé, Christopher Cantrell, Sebastien Dusanter, Bénédicte Picquet-Varrault, Alexandre Kukui, Abdelwahid Mellouki, Lucy J. Carpenter, Jos Lelieveld, and John N. Crowley
Atmos. Chem. Phys., 24, 11603–11618, https://doi.org/10.5194/acp-24-11603-2024, https://doi.org/10.5194/acp-24-11603-2024, 2024
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Using measurements of various trace gases in a suburban forest near Paris in the summer of 2022, we were able to gain insight into the sources and sinks of NOx (NO+NO2) with a special focus on their nighttime chemical and physical loss processes. NO was observed as a result of nighttime soil emissions when O3 levels were strongly depleted by deposition. NO oxidation products were not observed at night, indicating that soil and/or foliar surfaces are an efficient sink of reactive N.
Lee Tiszenkel, James H. Flynn, and Shan-Hu Lee
Atmos. Chem. Phys., 24, 11351–11363, https://doi.org/10.5194/acp-24-11351-2024, https://doi.org/10.5194/acp-24-11351-2024, 2024
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Ammonia and amines are important ingredients for aerosol formation in urban environments, but the measurements of these compounds are extremely challenging. Our observations show that urban ammonia and amines in Houston are emitted from urban sources, and diurnal variations in their concentrations are likely governed by gas-to-particle conversion and emissions.
Arpit Awasthi, Baerbel Sinha, Haseeb Hakkim, Sachin Mishra, Varkrishna Mummidivarapu, Gurmanjot Singh, Sachin D. Ghude, Vijay Kumar Soni, Narendra Nigam, Vinayak Sinha, and Madhavan N. Rajeevan
Atmos. Chem. Phys., 24, 10279–10304, https://doi.org/10.5194/acp-24-10279-2024, https://doi.org/10.5194/acp-24-10279-2024, 2024
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We use 111 volatile organic compounds (VOCs), PM10, and PM2.5 in a positive matrix factorization (PMF) model to resolve 11 pollution sources validated with chemical fingerprints. Crop residue burning and heating account for ~ 50 % of the PM, while traffic and industrial emissions dominate the gas-phase VOC burden and formation potential of secondary organic aerosols (> 60 %). Non-tailpipe emissions from compressed-natural-gas-fuelled commercial vehicles dominate the transport sector's PM burden.
Luke D. Schiferl, Cong Cao, Bronte Dalton, Andrew Hallward-Driemeier, Ricardo Toledo-Crow, and Róisín Commane
Atmos. Chem. Phys., 24, 10129–10142, https://doi.org/10.5194/acp-24-10129-2024, https://doi.org/10.5194/acp-24-10129-2024, 2024
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Carbon monoxide (CO) is an air pollutant and an important indicator of the incomplete combustion of fossil fuels in cities. Using 4 years of winter and spring observations in New York City, we found that both the magnitude and variability of CO from the metropolitan area are greater than expected. Transportation emissions cannot explain the missing and variable CO, which points to energy from buildings as a likely underappreciated source of urban air pollution and greenhouse gas emissions.
Chengzhi Xing, Cheng Liu, Chunxiang Ye, Jingkai Xue, Hongyu Wu, Xiangguang Ji, Jinping Ou, and Qihou Hu
Atmos. Chem. Phys., 24, 10093–10112, https://doi.org/10.5194/acp-24-10093-2024, https://doi.org/10.5194/acp-24-10093-2024, 2024
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We identified the contributions of ozone (O3) and nitrous acid (HONO) to the production rates of hydroxide (OH) in vertical space on the Tibetan Plateau (TP). A new insight was offered: the contributions of HONO and O3 to the production rates of OH on the TP are even greater than in lower-altitudes areas. This study enriches the understanding of vertical distribution of atmospheric components and explains the strong atmospheric oxidation capacity (AOC) on the TP.
Cited articles
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Davis, D. D., Eisele, F., Chen, G., Crawford, J., Huey, G., Tanner, D., Slusher, D., Mauldin, L., Oncley, S., Lenschow, D., Semmer, S., Shetter, R., Lefer, B., Arimoto, R., Hogan, A., Grube, P., Lazzara, M., Bandy, A., Thornton, D., Berresheim, H., Bingemer, H., Hutterli, M., McConnell, J., Bales, R., Dibb, J., Buhr, M., Park, J., McMurry, P., Swanson, A., Meinardi, S., and Blake, D.: An overview of ISCAT 2000, Atmos. Environ., 38, 5363–5373, 2004.
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Faloona, I. C., Tan, D., Lesher, R. L., Hazen, N. L., Frame, C. L., Simpas, J. B., Harder, H., Martinez, M., Di Carlo, P., Ren, X. R., and Brune, W. H.: A laser-induced fluorescence instrument for detecting tropospheric OH and HO2: Characteristics and calibration, J. Atmos. Chem., 47, 139–167, 2004.
France, J. L., King, M. D., Frey, M. M., Erbland, J., Picard, G., Preunkert, S., MacArthur, A., and Savarino, J.: Snow optical properties at Dome C (Concordia), Antarctica; implications for snow emissions and snow chemistry of reactive nitrogen, Atmos. Chem. Phys., 11, 9787–9801, https://doi.org/10.5194/acp-11-9787-2011, 2011.
Frey, M. M., Stewart, R. W., McConnell, J. R., and Bales, R. C.: Atmospheric hydroperoxides in West Antarctica: Links to stratospheric ozone and atmospheric oxidation capacity, J. Geophys. Res.-Atmos., 110, D23301, https://doi.org/10.1029/2005JD006110, 2005.
Frey, M. M., Brough, N., France, J. L., Anderson, P. S., Traulle, O., King, M. D., Jones, A. E., Wolff, E. W., and Savarino, J.: The diurnal variability of atmospheric nitrogen oxides (NO and NO2) above the Antarctic Plateau driven by atmospheric stability and snow emissions, Atmos. Chem. Phys., 13, 3045–3062, https://doi.org/10.5194/acp-13-3045-2013, 2013.
Frey, M. M., Roscoe, H. K., Kukui, A., Savarino, J., France, J. L., King, M. D., Legrand, M., and Preunkert, S.: Atmospheric nitrogen oxides (NO and NO2) at Dome C, East Antarctica, during the OPALE campaign, Atmos. Chem. Phys. Discuss., in preparation, 2014.
Fuchs, H., Holland, F., and Hofzumahaus, A.: Measurement of tropospheric RO2 and HO2 radicals by a laser-induced fluorescence instrument, Rev. Sci. Instrum., 79, 084104, https://doi.org/10.1063/1.2968712, 2008.
Gallée, H. and Gorodetskaya, I.: Validation of a limited area model over Dome C, Antarctic Plateau, during winter, 34, 61–72, Clim. Dynam., https://doi.org/10.1007/s00382-008-0499-y, 2008.
Gallée, H., Preunkert, S., Argentini, S., Frey, M. M., Genthon, C., Jourdain, B., Pietroni, I., Casasanta, G., Barral, H., Vignon, E., and Legrand, M.: Characterization of the boundary layer at Dome C (East Antarctica) during the OPALE summer campaign, Atmos. Chem. Phys. Discuss., in preparation, 2014.
Grannas, A. M., Jones, A. E., Dibb, J., Ammann, M., Anastasio, C., Beine, H. J., Bergin, M., Bottenheim, J., Boxe, C. S., Carver, G., Chen, G., Crawford, J. H., Dominé, F., Frey, M. M., Guzmán, M. I., Heard, D. E., Helmig, D., Hoffmann, M. R., Honrath, R. E., Huey, L. G., Hutterli, M., Jacobi, H. W., Klán, P., Lefer, B., McConnell, J., Plane, J., Sander, R., Savarino, J., Shepson, P. B., Simpson, W. R., Sodeau, J. R., von Glasow, R., Weller, R., Wolff, E. W., and Zhu, T.: An overview of snow photochemistry: evidence, mechanisms and impacts, Atmos. Chem. Phys., 7, 4329–4373, https://doi.org/10.5194/acp-7-4329-2007, 2007.
Hamer, P. D., Shallcross, D. E., and Frey, M. M.: Modelling the impact of oxygenated VOC and meteorology upon the boundary layer photochemistry at the South Pole, Atmos. Sci. Let., 8, 14–20, 2007.
Hanke, M., Uecker, J., Reiner, T., and Arnold, F.: Atmospheric peroxy radicals: ROXMAS, a new mass-spectrometric methodology for speciated measurements of HO2 and Sigma RO2 and first results, Int. J. Mass Spectrom., 213, 91–99, 2002.
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Legrand, M., Gros, V., Preunkert, S., Sarda-Estève, R., Thierry, A.-M., Pépy, G., and Jourdain, B.: A reassessment of the budget of formic and acetic acids in the boundary layer at Dumont d'Urville (coastal Antarctica): The role of penguin emissions on the budget of several oxygenated volatile organic compounds, J. Geophys. Res.-Atmos., 117, D06308, https://doi.org/10.1029/2011JD017102, 2012.
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Li, X., Rohrer, F., Hofzumahaus, A., Brauers, T., Häseler, R., Bohn, B., Broch, S., Fuchs, H., Gomm, S., Holland, F., Jäger, J., Kaiser, J., Keutsch, F. N., Lohse, I., Lu, K., Tillmann, R., Wegener, R., Wolfe, G. M., Mentel, T. F., Kiendler-Scharr, A., and Wahner, A.: Missing Gas-Phase Source of HONO Inferred from Zeppelin Measurements in the Troposphere, Science, 344, 292–296, 2014.
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Short summary
Concentrations of OH radicals and the sum of peroxy radicals, RO2, were measured in the boundary layer for the first time on the East Antarctic Plateau at the Concordia Station during the austral summer 2011/2012. The concentrations of radicals were comparable to those observed at the South Pole, confirming that the elevated oxidative capacity of the Antarctic atmospheric boundary layer found at the South Pole is not restricted to the South Pole but common over the high Antarctic plateau.
Concentrations of OH radicals and the sum of peroxy radicals, RO2, were measured in the boundary...
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