Articles | Volume 21, issue 16
https://doi.org/10.5194/acp-21-12413-2021
© Author(s) 2021. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/acp-21-12413-2021
© Author(s) 2021. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Research article
| 
19 Aug 2021
Research article |
| 19 Aug 2021
| 19 Aug 2021
Observation and modelling of ozone-destructive halogen chemistry in a passively degassing volcanic plume
Laboratoire de Physique et de Chimie de l’Environnement et de l’Espace, CNRS, Université d’Orléans, Orléans, France
LATMOS/IPSL, Sorbonne Université, UVSQ, CNRS, Paris, France
Department of Chemistry, University of Aberdeen, Aberdeen, UK
Tjarda Roberts
Laboratoire de Physique et de Chimie de l’Environnement et de l’Espace, CNRS, Université d’Orléans, Orléans, France
Slimane Bekki
LATMOS/IPSL, Sorbonne Université, UVSQ, CNRS, Paris, France
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Margot Clyne, Jean-Francois Lamarque, Michael J. Mills, Myriam Khodri, William Ball, Slimane Bekki, Sandip S. Dhomse, Nicolas Lebas, Graham Mann, Lauren Marshall, Ulrike Niemeier, Virginie Poulain, Alan Robock, Eugene Rozanov, Anja Schmidt, Andrea Stenke, Timofei Sukhodolov, Claudia Timmreck, Matthew Toohey, Fiona Tummon, Davide Zanchettin, Yunqian Zhu, and Owen B. Toon
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Clara Orbe, David A. Plummer, Darryn W. Waugh, Huang Yang, Patrick Jöckel, Douglas E. Kinnison, Beatrice Josse, Virginie Marecal, Makoto Deushi, Nathan Luke Abraham, Alexander T. Archibald, Martyn P. Chipperfield, Sandip Dhomse, Wuhu Feng, and Slimane Bekki
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Yuanhong Zhao, Marielle Saunois, Philippe Bousquet, Xin Lin, Antoine Berchet, Michaela I. Hegglin, Josep G. Canadell, Robert B. Jackson, Didier A. Hauglustaine, Sophie Szopa, Ann R. Stavert, Nathan Luke Abraham, Alex T. Archibald, Slimane Bekki, Makoto Deushi, Patrick Jöckel, Béatrice Josse, Douglas Kinnison, Ole Kirner, Virginie Marécal, Fiona M. O'Connor, David A. Plummer, Laura E. Revell, Eugene Rozanov, Andrea Stenke, Sarah Strode, Simone Tilmes, Edward J. Dlugokencky, and Bo Zheng
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In this study, we simulate the ultraviolet radiation evolution during the 21st century on Earth's surface using the output from several numerical models which participated in the Chemistry-Climate Model Initiative. We present four possible futures which depend on greenhouse gases emissions. The role of ozone-depleting substances, greenhouse gases and aerosols are investigated. Our results emphasize the important role of aerosols for future ultraviolet radiation in the Northern Hemisphere.
Sophie Szopa, Rémi Thiéblemont, Slimane Bekki, Svetlana Botsyun, and Pierre Sepulchre
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The stratospheric ozone layer plays a key role in atmospheric thermal structure and circulation. Here, with a chemistry–climate model, we evaluate the potential role of stratospheric ozone chemistry in the case of Eocene hot conditions. Our results suggest that using stratospheric ozone calculated by the modeled Eocene conditions instead of the commonly specified preindustrial ozone distribution could change the simulated global surface air temperature by as much as 14 %.
Tommaso Galeazzo, Slimane Bekki, Erwan Martin, Joël Savarino, and Stephen R. Arnold
Atmos. Chem. Phys., 18, 17909–17931, https://doi.org/10.5194/acp-18-17909-2018, https://doi.org/10.5194/acp-18-17909-2018, 2018
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Volcanic sulfur can have climatic impacts for the planet via sulfate aerosol formation, leading also to pollution events. We provide model constraints on tropospheric volcanic sulfate formation, with implications for its lifetime and impacts on regional air quality. Oxygen isotope investigations from our model suggest that in the poor tropospheric plumes of halogens, the O2/TMI sulfur oxidation pathway might significantly control sulfate production. The produced sulfate has no isotopic anomaly.
Amanda C. Maycock, Katja Matthes, Susann Tegtmeier, Hauke Schmidt, Rémi Thiéblemont, Lon Hood, Hideharu Akiyoshi, Slimane Bekki, Makoto Deushi, Patrick Jöckel, Oliver Kirner, Markus Kunze, Marion Marchand, Daniel R. Marsh, Martine Michou, David Plummer, Laura E. Revell, Eugene Rozanov, Andrea Stenke, Yousuke Yamashita, and Kohei Yoshida
Atmos. Chem. Phys., 18, 11323–11343, https://doi.org/10.5194/acp-18-11323-2018, https://doi.org/10.5194/acp-18-11323-2018, 2018
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The 11-year solar cycle is an important driver of climate variability. Changes in incoming solar ultraviolet radiation affect atmospheric ozone, which in turn influences atmospheric temperatures. Constraining the impact of the solar cycle on ozone is therefore important for understanding climate variability. This study examines the representation of the solar influence on ozone in numerical models used to simulate past and future climate. We highlight important differences among model datasets.
Blanca Ayarzagüena, Lorenzo M. Polvani, Ulrike Langematz, Hideharu Akiyoshi, Slimane Bekki, Neal Butchart, Martin Dameris, Makoto Deushi, Steven C. Hardiman, Patrick Jöckel, Andrew Klekociuk, Marion Marchand, Martine Michou, Olaf Morgenstern, Fiona M. O'Connor, Luke D. Oman, David A. Plummer, Laura Revell, Eugene Rozanov, David Saint-Martin, John Scinocca, Andrea Stenke, Kane Stone, Yousuke Yamashita, Kohei Yoshida, and Guang Zeng
Atmos. Chem. Phys., 18, 11277–11287, https://doi.org/10.5194/acp-18-11277-2018, https://doi.org/10.5194/acp-18-11277-2018, 2018
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Stratospheric sudden warmings (SSWs) are natural major disruptions of the polar stratospheric circulation that also affect surface weather. In the literature there are conflicting claims as to whether SSWs will change in the future. The confusion comes from studies using different models and methods. Here we settle the question by analysing 12 models with a consistent methodology, to show that no robust changes in frequency and other features are expected over the 21st century.
Sandip S. Dhomse, Douglas Kinnison, Martyn P. Chipperfield, Ross J. Salawitch, Irene Cionni, Michaela I. Hegglin, N. Luke Abraham, Hideharu Akiyoshi, Alex T. Archibald, Ewa M. Bednarz, Slimane Bekki, Peter Braesicke, Neal Butchart, Martin Dameris, Makoto Deushi, Stacey Frith, Steven C. Hardiman, Birgit Hassler, Larry W. Horowitz, Rong-Ming Hu, Patrick Jöckel, Beatrice Josse, Oliver Kirner, Stefanie Kremser, Ulrike Langematz, Jared Lewis, Marion Marchand, Meiyun Lin, Eva Mancini, Virginie Marécal, Martine Michou, Olaf Morgenstern, Fiona M. O'Connor, Luke Oman, Giovanni Pitari, David A. Plummer, John A. Pyle, Laura E. Revell, Eugene Rozanov, Robyn Schofield, Andrea Stenke, Kane Stone, Kengo Sudo, Simone Tilmes, Daniele Visioni, Yousuke Yamashita, and Guang Zeng
Atmos. Chem. Phys., 18, 8409–8438, https://doi.org/10.5194/acp-18-8409-2018, https://doi.org/10.5194/acp-18-8409-2018, 2018
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We analyse simulations from the Chemistry-Climate Model Initiative (CCMI) to estimate the return dates of the stratospheric ozone layer from depletion by anthropogenic chlorine and bromine. The simulations from 20 models project that global column ozone will return to 1980 values in 2047 (uncertainty range 2042–2052). Return dates in other regions vary depending on factors related to climate change and importance of chlorine and bromine. Column ozone in the tropics may continue to decline.
Dunya Alraddawi, Alain Sarkissian, Philippe Keckhut, Olivier Bock, Stefan Noël, Slimane Bekki, Abdenour Irbah, Mustapha Meftah, and Chantal Claud
Atmos. Meas. Tech., 11, 2949–2965, https://doi.org/10.5194/amt-11-2949-2018, https://doi.org/10.5194/amt-11-2949-2018, 2018
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The current study provides intercomparisons of various water vapour measurements in the Arctic. It compares ground-based GPS observations with satellite measurements in the infrared (IR), near-infrared (NIR) and visible (VIS) through a specific method allowing us to quantify their uncertainties and limits.
Unlike IR, satellite observations in NIR and VIS bands are mostly sensible to cloud cover during summer and to albedo variability over canopy or polluted snow-covered surfaces in winter.
Luke Surl, Paul I. Palmer, and Gonzalo González Abad
Atmos. Chem. Phys., 18, 4549–4566, https://doi.org/10.5194/acp-18-4549-2018, https://doi.org/10.5194/acp-18-4549-2018, 2018
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We used observations of HCHO formaldehyde columns from the OMI satellite instrument and the GEOS-Chem atmospheric chemistry model to investigate how and why HCHO varies over India. We find that emissions of biogenic VOC from forests are the most powerful driver, with forests' response to seasonal temperature variations causing variation over time. Human-driven emissions of VOC and burning of vegetation have detectable, but more limited, impacts.
Thibaut Lurton, Fabrice Jégou, Gwenaël Berthet, Jean-Baptiste Renard, Lieven Clarisse, Anja Schmidt, Colette Brogniez, and Tjarda J. Roberts
Atmos. Chem. Phys., 18, 3223–3247, https://doi.org/10.5194/acp-18-3223-2018, https://doi.org/10.5194/acp-18-3223-2018, 2018
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We quantify the chemical and microphysical effects of volcanic SO2 and HCl from the June 2009 Sarychev Peak eruption using a comprehensive aerosol–chemistry model combined with in situ measurements and satellite retrievals. Our results suggest that previous studies underestimated the eruption's atmospheric and climatic impact, mainly because previous model-to-satellite comparisons had to make assumptions about the aerosol size distribution and were based on biased satellite retrievals of AOD.
Lauren Marshall, Anja Schmidt, Matthew Toohey, Ken S. Carslaw, Graham W. Mann, Michael Sigl, Myriam Khodri, Claudia Timmreck, Davide Zanchettin, William T. Ball, Slimane Bekki, James S. A. Brooke, Sandip Dhomse, Colin Johnson, Jean-Francois Lamarque, Allegra N. LeGrande, Michael J. Mills, Ulrike Niemeier, James O. Pope, Virginie Poulain, Alan Robock, Eugene Rozanov, Andrea Stenke, Timofei Sukhodolov, Simone Tilmes, Kostas Tsigaridis, and Fiona Tummon
Atmos. Chem. Phys., 18, 2307–2328, https://doi.org/10.5194/acp-18-2307-2018, https://doi.org/10.5194/acp-18-2307-2018, 2018
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We use four global aerosol models to compare the simulated sulfate deposition from the 1815 Mt. Tambora eruption to ice core records. Inter-model volcanic sulfate deposition differs considerably. Volcanic sulfate deposited on polar ice sheets is used to estimate the atmospheric sulfate burden and subsequently radiative forcing of historic eruptions. Our results suggest that deriving such relationships from model simulations may be associated with greater uncertainties than previously thought.
Christoph Kleinschmitt, Olivier Boucher, Slimane Bekki, François Lott, and Ulrich Platt
Geosci. Model Dev., 10, 3359–3378, https://doi.org/10.5194/gmd-10-3359-2017, https://doi.org/10.5194/gmd-10-3359-2017, 2017
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Stratospheric aerosols play an important role in the climate system by affecting the Earth's radiative budget. In this article we present the newly developed LMDZ-S3A model and assess its performance against observations in periods of low and high aerosol loading. The model may serve as a tool to study the climate impacts of volcanic eruptions, as well as the deliberate injection of aerosols into the stratosphere, which has been proposed as a method of geoengineering to abate global warming.
Rémi Thiéblemont, Marion Marchand, Slimane Bekki, Sébastien Bossay, Franck Lefèvre, Mustapha Meftah, and Alain Hauchecorne
Atmos. Chem. Phys., 17, 9897–9916, https://doi.org/10.5194/acp-17-9897-2017, https://doi.org/10.5194/acp-17-9897-2017, 2017
Kevin M. Smalley, Andrew E. Dessler, Slimane Bekki, Makoto Deushi, Marion Marchand, Olaf Morgenstern, David A. Plummer, Kiyotaka Shibata, Yousuke Yamashita, and Guang Zeng
Atmos. Chem. Phys., 17, 8031–8044, https://doi.org/10.5194/acp-17-8031-2017, https://doi.org/10.5194/acp-17-8031-2017, 2017
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This paper explains a new way to evaluate simulated lower-stratospheric water vapor. We use a multivariate linear regression to predict 21st century lower stratospheric water vapor within 12 chemistry climate models using tropospheric warming, the Brewer–Dobson circulation, and the quasi-biennial oscillation as predictors. This methodology produce strong fits to simulated water vapor, and potentially represents a superior method to evaluate model trends in lower-stratospheric water vapor.
Gwenaël Berthet, Fabrice Jégou, Valéry Catoire, Gisèle Krysztofiak, Jean-Baptiste Renard, Adam E. Bourassa, Doug A. Degenstein, Colette Brogniez, Marcel Dorf, Sebastian Kreycy, Klaus Pfeilsticker, Bodo Werner, Franck Lefèvre, Tjarda J. Roberts, Thibaut Lurton, Damien Vignelles, Nelson Bègue, Quentin Bourgeois, Daniel Daugeron, Michel Chartier, Claude Robert, Bertrand Gaubicher, and Christophe Guimbaud
Atmos. Chem. Phys., 17, 2229–2253, https://doi.org/10.5194/acp-17-2229-2017, https://doi.org/10.5194/acp-17-2229-2017, 2017
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Since the last major volcanic event, i.e. the Pinatubo eruption in 1991, only
moderateeruptions have regularly injected sulfur into the stratosphere, typically enhancing the aerosol loading for several months. We investigate here for the first time the chemical perturbation associated with the Sarychev eruption in June 2009, using balloon-borne instruments and model calculations. Some chemical compounds are significantly affected by the aerosols, but the impact on stratospheric ozone is weak.
Olaf Morgenstern, Michaela I. Hegglin, Eugene Rozanov, Fiona M. O'Connor, N. Luke Abraham, Hideharu Akiyoshi, Alexander T. Archibald, Slimane Bekki, Neal Butchart, Martyn P. Chipperfield, Makoto Deushi, Sandip S. Dhomse, Rolando R. Garcia, Steven C. Hardiman, Larry W. Horowitz, Patrick Jöckel, Beatrice Josse, Douglas Kinnison, Meiyun Lin, Eva Mancini, Michael E. Manyin, Marion Marchand, Virginie Marécal, Martine Michou, Luke D. Oman, Giovanni Pitari, David A. Plummer, Laura E. Revell, David Saint-Martin, Robyn Schofield, Andrea Stenke, Kane Stone, Kengo Sudo, Taichu Y. Tanaka, Simone Tilmes, Yousuke Yamashita, Kohei Yoshida, and Guang Zeng
Geosci. Model Dev., 10, 639–671, https://doi.org/10.5194/gmd-10-639-2017, https://doi.org/10.5194/gmd-10-639-2017, 2017
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We present a review of the make-up of 20 models participating in the Chemistry–Climate Model Initiative (CCMI). In comparison to earlier such activities, most of these models comprise a whole-atmosphere chemistry, and several of them include an interactive ocean module. This makes them suitable for studying the interactions of tropospheric air quality, stratospheric ozone, and climate. The paper lays the foundation for other studies using the CCMI simulations for scientific analysis.
Tjarda J. Roberts, Marina Dütsch, Lars R. Hole, and Paul B. Voss
Atmos. Chem. Phys., 16, 12383–12396, https://doi.org/10.5194/acp-16-12383-2016, https://doi.org/10.5194/acp-16-12383-2016, 2016
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We present Controlled Meteorological (CMET) balloon flights in the Arctic. CMETs are a novel balloon that can be controlled (by satellite link) to change altitude during the flight and remain in the troposphere up to several days. We performed automated repeated soundings in the Arctic boundary layer during the flight and compared the observations (temperature, humidity, wind) to output from two atmospheric models. CMETs are a valuable tool for probing the lower atmosphere in remote regions.
Line Jourdain, Tjarda Jane Roberts, Michel Pirre, and Beatrice Josse
Atmos. Chem. Phys., 16, 12099–12125, https://doi.org/10.5194/acp-16-12099-2016, https://doi.org/10.5194/acp-16-12099-2016, 2016
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Ambrym Volcano (Vanuatu, southwest Pacific) is one of the largest sources of continuous volcanic emissions worldwide. We performed a modeling study that confirms the strong influence of Ambrym emissions during an extreme degassing event of early 2005 on the composition of the atmosphere on the local and regional scales. It also stresses the importance of considering reactive halogen chemistry in the volcanic plume when assessing the impact of volcanic emissions on climate.
Davide Zanchettin, Myriam Khodri, Claudia Timmreck, Matthew Toohey, Anja Schmidt, Edwin P. Gerber, Gabriele Hegerl, Alan Robock, Francesco S. R. Pausata, William T. Ball, Susanne E. Bauer, Slimane Bekki, Sandip S. Dhomse, Allegra N. LeGrande, Graham W. Mann, Lauren Marshall, Michael Mills, Marion Marchand, Ulrike Niemeier, Virginie Poulain, Eugene Rozanov, Angelo Rubino, Andrea Stenke, Kostas Tsigaridis, and Fiona Tummon
Geosci. Model Dev., 9, 2701–2719, https://doi.org/10.5194/gmd-9-2701-2016, https://doi.org/10.5194/gmd-9-2701-2016, 2016
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Simulating volcanically-forced climate variability is a challenging task for climate models. The Model Intercomparison Project on the climatic response to volcanic forcing (VolMIP) – an endorsed contribution to CMIP6 – defines a protocol for idealized volcanic-perturbation experiments to improve comparability of results across different climate models. This paper illustrates the design of VolMIP's experiments and describes the aerosol forcing input datasets to be used.
Jean-Baptiste Renard, François Dulac, Gwenaël Berthet, Thibaut Lurton, Damien Vignelles, Fabrice Jégou, Thierry Tonnelier, Matthieu Jeannot, Benoit Couté, Rony Akiki, Nicolas Verdier, Marc Mallet, François Gensdarmes, Patrick Charpentier, Samuel Mesmin, Vincent Duverger, Jean-Charles Dupont, Thierry Elias, Vincent Crenn, Jean Sciare, Paul Zieger, Matthew Salter, Tjarda Roberts, Jérôme Giacomoni, Matthieu Gobbi, Eric Hamonou, Haraldur Olafsson, Pavla Dagsson-Waldhauserova, Claude Camy-Peyret, Christophe Mazel, Thierry Décamps, Martin Piringer, Jérémy Surcin, and Daniel Daugeron
Atmos. Meas. Tech., 9, 3673–3686, https://doi.org/10.5194/amt-9-3673-2016, https://doi.org/10.5194/amt-9-3673-2016, 2016
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We illustrate the first Light Optical Aerosol Counter (LOAC) airborne results obtained from an unmanned aerial vehicle (UAV) and a variety of scientific balloons: tethered balloons deployed in urban environments, pressurized balloons drifting in the lower troposphere over the western Mediterranean during the Chemistry-Aerosol Mediterranean Experiment (ChArMEx), and meteorological sounding balloons launched in the western Mediterranean region and in the south-west of France.
Jean-Baptiste Renard, François Dulac, Gwenaël Berthet, Thibaut Lurton, Damien Vignelles, Fabrice Jégou, Thierry Tonnelier, Matthieu Jeannot, Benoit Couté, Rony Akiki, Nicolas Verdier, Marc Mallet, François Gensdarmes, Patrick Charpentier, Samuel Mesmin, Vincent Duverger, Jean-Charles Dupont, Thierry Elias, Vincent Crenn, Jean Sciare, Paul Zieger, Matthew Salter, Tjarda Roberts, Jérôme Giacomoni, Matthieu Gobbi, Eric Hamonou, Haraldur Olafsson, Pavla Dagsson-Waldhauserova, Claude Camy-Peyret, Christophe Mazel, Thierry Décamps, Martin Piringer, Jérémy Surcin, and Daniel Daugeron
Atmos. Meas. Tech., 9, 1721–1742, https://doi.org/10.5194/amt-9-1721-2016, https://doi.org/10.5194/amt-9-1721-2016, 2016
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LOAC is a light aerosols counter for performing measurements at the surface and under all kinds of atmospheric balloons. LOAC performs observations at two scattering angles. The first one at 12° is insensitive to the refractive index of the particles; the second one at 60° is strongly sensitive to the refractive index. By combining the measurements, it is possible to retrieve the size distribution between 0.2 and 100 micrometeres and to estimate the nature of the dominant particles.
L. Surl, D. Donohoue, A. Aiuppa, N. Bobrowski, and R. von Glasow
Atmos. Chem. Phys., 15, 2613–2628, https://doi.org/10.5194/acp-15-2613-2015, https://doi.org/10.5194/acp-15-2613-2015, 2015
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We investigate the atmospheric chemistry that occurs in the plume of Mt. Etna shortly after emission.
We measured O3 destruction in the plume. Using simultaneous measurements of SO2 and wind speed, we approximate the rate of this destruction. BrO, expected to be an indicator of ozone-destructive chemistry, is also detected.
A computer model is able to approximately reproduce these results and is used to make inferences about the chemistry occurring that cannot be directly observed.
T. J. Roberts, L. Jourdain, P. T. Griffiths, and M. Pirre
Atmos. Chem. Phys., 14, 11185–11199, https://doi.org/10.5194/acp-14-11185-2014, https://doi.org/10.5194/acp-14-11185-2014, 2014
T. J. Roberts, R. S. Martin, and L. Jourdain
Atmos. Chem. Phys., 14, 11201–11219, https://doi.org/10.5194/acp-14-11201-2014, https://doi.org/10.5194/acp-14-11201-2014, 2014
L. Grellier, V. Marécal, B. Josse, P. D. Hamer, T. J. Roberts, A. Aiuppa, and M. Pirre
Geosci. Model Dev. Discuss., https://doi.org/10.5194/gmdd-7-2581-2014, https://doi.org/10.5194/gmdd-7-2581-2014, 2014
Revised manuscript not accepted
Related subject area
Subject: Gases | Research Activity: Atmospheric Modelling and Data Analysis | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Seasonal, regional, and vertical characteristics of high-carbon-monoxide plumes along with their associated ozone anomalies, as seen by IAGOS between 2002 and 2019
The potential of drone observations to improve air quality predictions by 4D-Var
Process analysis of elevated concentrations of organic acids at Whiteface Mountain, New York
Ozone source attribution in polluted European areas during summer 2017 as simulated with MECO(n)
Opinion: Challenges and needs of tropospheric chemical mechanism development
The atmospheric oxidizing capacity in China – Part 2: Sensitivity to emissions of primary pollutants
Role of chemical production and depositional losses on formaldehyde in the Community Regional Atmospheric Chemistry Multiphase Mechanism (CRACMM)
Review of source analyses of ambient volatile organic compounds considering reactive losses: methods of reducing loss effects, impacts of losses, and sources
Interpreting summertime hourly variation of NO2 columns with implications for geostationary satellite applications
An investigation into atmospheric nitrous acid (HONO) processes in South Korea
Performance evaluation of UKESM1 for surface ozone across the pan-tropics
Constraining light dependency in modeled emissions through comparison to observed biogenic volatile organic compound (BVOC) concentrations in a southeastern US forest
A global re-analysis of regionally resolved emissions and atmospheric mole fractions of SF6 for the period 2005–2021
Tropospheric ozone precursors: global and regional distributions, trends, and variability
The contribution of transport emissions to ozone mixing ratios and methane lifetime in 2015 and 2050 in the Shared Socioeconomic Pathways (SSPs)
Ether and ester formation from peroxy radical recombination: a qualitative reaction channel analysis
ACEIC: a comprehensive anthropogenic chlorine emission inventory for China
Impact of methane and other precursor emission reductions on surface ozone in Europe: scenario analysis using the European Monitoring and Evaluation Programme (EMEP) Meteorological Synthesizing Centre – West (MSC-W) model
Verifying national inventory-based combustion emissions of CO2 across the UK and mainland Europe using satellite observations of atmospheric CO and CO2
An improved estimate of inorganic iodine emissions from the ocean using a coupled surface microlayer box model
Impact of improved representation of volatile organic compound emissions and production of NOx reservoirs on modeled urban ozone production
The effect of different climate and air quality policies in China on in situ ozone production in Beijing
Assessing the relative impacts of satellite ozone and its precursor observations to improve global tropospheric ozone analysis using multiple chemical reanalysis systems
Evaluating present-day and future impacts of agricultural ammonia emissions on atmospheric chemistry and climate
Enhancing long-term trend simulation of the global tropospheric hydroxyl (TOH) and its drivers from 2005 to 2019: a synergistic integration of model simulations and satellite observations
Intercomparison of GEOS-Chem and CAM-chem tropospheric oxidant chemistry within the Community Earth System Model version 2 (CESM2)
Development of a detailed gaseous oxidation scheme of naphthalene for secondary organic aerosol (SOA) formation and speciation
Air pollution satellite-based CO2 emission inversion: system evaluation, sensitivity analysis, and future perspective
Anthropogenic emission controls reduce summertime ozone-temperature sensitivity in the United States
Large contributions of soil emissions to the atmospheric nitrogen budget and their impacts on air quality and temperature rise in North China
Why did ozone concentrations remain high during Shanghai's static management? A statistical and radical-chemistry perspective
Impact of introducing electric vehicles on ground-level O3 and PM2.5 in the Greater Tokyo Area: Yearly trends and the importance of changes in the Urban Heat Island effect
Revising VOC emissions speciation improves the simulation of global background ethane and propane
Changes in South American surface ozone trends: exploring the influences of precursors and extreme events
Evaluating NOx stack plume emissions using a high-resolution atmospheric chemistry model and satellite-derived NO2 columns
NOx emissions in France in 2019–2021 as estimated by the high-spatial-resolution assimilation of TROPOMI NO2 observations
Urban ozone formation and sensitivities to volatile chemical products, cooking emissions, and NOx across the Los Angeles Basin
Aggravated surface O3 pollution primarily driven by meteorological variations in China during the 2020 COVID-19 pandemic lockdown period
Identifying decadal trends in deweathered concentrations of criteria air pollutants in Canadian urban atmospheres with machine learning approaches
Evaluation of modelled versus observed non-methane volatile organic compounds at European Monitoring and Evaluation Programme sites in Europe
Constraining non-methane VOC emissions with TROPOMI HCHO observations: impact on summertime ozone simulation in August 2022 in China
Insights on ozone pollution control in urban areas by decoupling meteorological factors based on machine learning
Revealing the significant acceleration of hydrofluorocarbon (HFC) emissions in eastern Asia through long-term atmospheric observations
Interpreting Geostationary Environment Monitoring Spectrometer (GEMS) geostationary satellite observations of the diurnal variation in nitrogen dioxide (NO2) over East Asia
An intercomparison of satellite, airborne, and ground-level observations with WRF–CAMx simulations of NO2 columns over Houston, Texas, during the September 2021 TRACER-AQ campaign
Investigating processes influencing simulation of local Arctic wintertime anthropogenic pollution in Fairbanks, Alaska during ALPACA-2022
Interannual variability of summertime formaldehyde (HCHO) vertical column density and its main drivers at northern high latitudes
The impact of multi-decadal changes in VOC speciation on urban ozone chemistry: a case study in Birmingham, United Kingdom
Technical note: Challenges in detecting free tropospheric ozone trends in a sparsely sampled environment
Combined assimilation of NOAA surface and MIPAS satellite observations to constrain the global budget of carbonyl sulfide
Thibaut Lebourgeois, Bastien Sauvage, Pawel Wolff, Béatrice Josse, Virginie Marécal, Yasmine Bennouna, Romain Blot, Damien Boulanger, Hannah Clark, Jean-Marc Cousin, Philippe Nedelec, and Valérie Thouret
Atmos. Chem. Phys., 24, 13975–14004, https://doi.org/10.5194/acp-24-13975-2024, https://doi.org/10.5194/acp-24-13975-2024, 2024
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Our study examines intense-carbon-monoxide (CO) pollution events measured by commercial aircraft from the In-service Aircraft for a Global Observing System (IAGOS) research infrastructure. We combine these measurements with the SOFT-IO model to trace the origin of the observed CO. A comprehensive analysis of the geographical origin, source type, seasonal variation, and ozone levels of these pollution events is provided.
Hassnae Erraji, Philipp Franke, Astrid Lampert, Tobias Schuldt, Ralf Tillmann, Andreas Wahner, and Anne Caroline Lange
Atmos. Chem. Phys., 24, 13913–13934, https://doi.org/10.5194/acp-24-13913-2024, https://doi.org/10.5194/acp-24-13913-2024, 2024
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Four-dimensional variational data assimilation allows for the simultaneous optimisation of initial values and emission rates by using trace-gas profiles from drone observations in a regional air quality model. Assimilated profiles positively impact the representation of air pollutants in the model by improving their vertical distribution and ground-level concentrations. This case study highlights the potential of drone data to enhance air quality analyses including local emission evaluation.
Christopher Lawrence, Mary Barth, John Orlando, Paul Casson, Richard Brandt, Daniel Kelting, Elizabeth Yerger, and Sara Lance
Atmos. Chem. Phys., 24, 13693–13713, https://doi.org/10.5194/acp-24-13693-2024, https://doi.org/10.5194/acp-24-13693-2024, 2024
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This work uses chemical transport and box modeling to study the gas- and aqueous-phase production of organic acid concentrations measured in cloud water at the summit of Whiteface Mountain on 1 July 2018. Isoprene was the major source of formic, acetic, and oxalic acid. Gas-phase chemistry greatly underestimated formic and acetic acid, indicating missing sources, while cloud chemistry was a key source of oxalic acid. More studies of organic acids are required to better constrain their sources.
Markus Kilian, Volker Grewe, Patrick Jöckel, Astrid Kerkweg, Mariano Mertens, Andreas Zahn, and Helmut Ziereis
Atmos. Chem. Phys., 24, 13503–13523, https://doi.org/10.5194/acp-24-13503-2024, https://doi.org/10.5194/acp-24-13503-2024, 2024
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Anthropogenic emissions are a major source of precursors of tropospheric ozone. As ozone formation is highly non-linear, we apply a global–regional chemistry–climate model with a source attribution method (tagging) to quantify the contribution of anthropogenic emissions to ozone. Our analysis shows that the contribution of European anthropogenic emissions largely increases during large ozone periods, indicating that emissions from these sectors drive ozone values.
Barbara Ervens, Andrew Rickard, Bernard Aumont, William P. L. Carter, Max McGillen, Abdelwahid Mellouki, John Orlando, Bénédicte Picquet-Varrault, Paul Seakins, William R. Stockwell, Luc Vereecken, and Timothy J. Wallington
Atmos. Chem. Phys., 24, 13317–13339, https://doi.org/10.5194/acp-24-13317-2024, https://doi.org/10.5194/acp-24-13317-2024, 2024
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Chemical mechanisms describe the chemical processes in atmospheric models that are used to describe the changes in the atmospheric composition. Therefore, accurate chemical mechanisms are necessary to predict the evolution of air pollution and climate change. The article describes all steps that are needed to build chemical mechanisms and discusses the advances and needs of experimental and theoretical research activities needed to build reliable chemical mechanisms.
Jianing Dai, Guy P. Brasseur, Mihalis Vrekoussis, Maria Kanakidou, Kun Qu, Yijuan Zhang, Hongliang Zhang, and Tao Wang
Atmos. Chem. Phys., 24, 12943–12962, https://doi.org/10.5194/acp-24-12943-2024, https://doi.org/10.5194/acp-24-12943-2024, 2024
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This paper employs a regional chemical transport model to quantify the sensitivity of air pollutants and photochemical parameters to specified emission reductions in China for representative winter and summer conditions. The study provides insights into further air quality control in China with reduced primary emissions.
T. Nash Skipper, Emma L. D'Ambro, Forwood C. Wiser, V. Faye McNeill, Rebecca H. Schwantes, Barron H. Henderson, Ivan R. Piletic, Colleen B. Baublitz, Jesse O. Bash, Andrew R. Whitehill, Lukas C. Valin, Asher P. Mouat, Jennifer Kaiser, Glenn M. Wolfe, Jason M. St. Clair, Thomas F. Hanisco, Alan Fried, Bryan K. Place, and Havala O.T. Pye
Atmos. Chem. Phys., 24, 12903–12924, https://doi.org/10.5194/acp-24-12903-2024, https://doi.org/10.5194/acp-24-12903-2024, 2024
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We develop the Community Regional Atmospheric Chemistry Multiphase Mechanism (CRACMM) version 2 to improve predictions of formaldehyde in ambient air compared to satellite-, aircraft-, and ground-based observations. With the updated chemistry, we estimate the cancer risk from inhalation exposure to ambient formaldehyde across the contiguous USA and predict that 40 % of this risk is controllable through reductions in anthropogenic emissions of nitrogen oxides and reactive organic carbon.
Baoshuang Liu, Yao Gu, Yutong Wu, Qili Dai, Shaojie Song, Yinchang Feng, and Philip K. Hopke
Atmos. Chem. Phys., 24, 12861–12879, https://doi.org/10.5194/acp-24-12861-2024, https://doi.org/10.5194/acp-24-12861-2024, 2024
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Reactive loss of volatile organic compounds (VOCs) is a long-term issue yet to be resolved in VOC source analyses. We assess common methods of, and existing issues in, reducing losses, impacts of losses, and sources in current source analyses. We offer a potential supporting role for solving issues of VOC conversion. Source analyses of consumed VOCs that reacted to produce ozone and secondary organic aerosols can play an important role in the effective control of secondary pollution in air.
Deepangsu Chatterjee, Randall V. Martin, Chi Li, Dandan Zhang, Haihui Zhu, Daven K. Henze, James H. Crawford, Ronald C. Cohen, Lok N. Lamsal, and Alexander M. Cede
Atmos. Chem. Phys., 24, 12687–12706, https://doi.org/10.5194/acp-24-12687-2024, https://doi.org/10.5194/acp-24-12687-2024, 2024
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We investigate the hourly variation of NO2 columns and surface concentrations by applying the GEOS-Chem model to interpret aircraft and ground-based measurements over the US and Pandora sun photometer measurements over the US, Europe, and Asia. Corrections to the Pandora columns and finer model resolution improve the modeled representation of the summertime hourly variation of total NO2 columns to explain the weaker hourly variation in NO2 columns than at the surface.
Kiyeon Kim, Kyung Man Han, Chul Han Song, Hyojun Lee, Ross Beardsley, Jinhyeok Yu, Greg Yarwood, Bonyoung Koo, Jasper Madalipay, Jung-Hun Woo, and Seogju Cho
Atmos. Chem. Phys., 24, 12575–12593, https://doi.org/10.5194/acp-24-12575-2024, https://doi.org/10.5194/acp-24-12575-2024, 2024
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We incorporated each HONO process into the current CMAQ modeling framework to enhance the accuracy of HONO mixing ratio predictions. These results expand our understanding of HONO photochemistry and identify crucial sources of HONO that impact the total HONO budget in Seoul, South Korea. Through this investigation, we contribute to resolving discrepancies in understanding chemical transport models, with implications for better air quality management and environmental protection in the region.
Flossie Brown, Gerd Folberth, Stephen Sitch, Paulo Artaxo, Marijn Bauters, Pascal Boeckx, Alexander W. Cheesman, Matteo Detto, Ninong Komala, Luciana Rizzo, Nestor Rojas, Ines dos Santos Vieira, Steven Turnock, Hans Verbeeck, and Alfonso Zambrano
Atmos. Chem. Phys., 24, 12537–12555, https://doi.org/10.5194/acp-24-12537-2024, https://doi.org/10.5194/acp-24-12537-2024, 2024
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Ozone is a pollutant that is detrimental to human and plant health. Ozone monitoring sites in the tropics are limited, so models are often used to understand ozone exposure. We use measurements from the tropics to evaluate ozone from the UK Earth system model, UKESM1. UKESM1 is able to capture the pattern of ozone in the tropics, except in southeast Asia, although it systematically overestimates it at all sites. This work highlights that UKESM1 can capture seasonal and hourly variability.
Namrata Shanmukh Panji, Deborah F. McGlynn, Laura E. R. Barry, Todd M. Scanlon, Manuel T. Lerdau, Sally E. Pusede, and Gabriel Isaacman-VanWertz
Atmos. Chem. Phys., 24, 12495–12507, https://doi.org/10.5194/acp-24-12495-2024, https://doi.org/10.5194/acp-24-12495-2024, 2024
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Climate change will bring about changes in parameters that are currently used in global-scale models to calculate biogenic emissions. This study seeks to understand the factors driving these models by comparing long-term datasets of biogenic compounds to modeled emissions. We note that the light-dependent fractions currently used in models do not accurately represent regional observations. We provide evidence for the time-dependent variation in this parameter for future modifications to models.
Martin Vojta, Andreas Plach, Saurabh Annadate, Sunyoung Park, Gawon Lee, Pallav Purohit, Florian Lindl, Xin Lan, Jens Mühle, Rona L. Thompson, and Andreas Stohl
Atmos. Chem. Phys., 24, 12465–12493, https://doi.org/10.5194/acp-24-12465-2024, https://doi.org/10.5194/acp-24-12465-2024, 2024
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We constrain the global emissions of the very potent greenhouse gas sulfur hexafluoride (SF6) between 2005 and 2021. We show that SF6 emissions are decreasing in the USA and in the EU, while they are substantially growing in China, leading overall to an increasing global emission trend. The national reports for the USA, EU, and China all underestimated their SF6 emissions. However, stringent mitigation measures can successfully reduce SF6 emissions, as can be seen in the EU emission trend.
Yasin Elshorbany, Jerald R. Ziemke, Sarah Strode, Hervé Petetin, Kazuyuki Miyazaki, Isabelle De Smedt, Kenneth Pickering, Rodrigo J. Seguel, Helen Worden, Tamara Emmerichs, Domenico Taraborrelli, Maria Cazorla, Suvarna Fadnavis, Rebecca R. Buchholz, Benjamin Gaubert, Néstor Y. Rojas, Thiago Nogueira, Thérèse Salameh, and Min Huang
Atmos. Chem. Phys., 24, 12225–12257, https://doi.org/10.5194/acp-24-12225-2024, https://doi.org/10.5194/acp-24-12225-2024, 2024
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We investigated tropospheric ozone spatial variability and trends from 2005 to 2019 and related those to ozone precursors on global and regional scales. We also investigate the spatiotemporal characteristics of the ozone formation regime in relation to ozone chemical sources and sinks. Our analysis is based on remote sensing products of the tropospheric column of ozone and its precursors, nitrogen dioxide, formaldehyde, and total column CO, as well as ozonesonde data and model simulations.
Mariano Mertens, Sabine Brinkop, Phoebe Graf, Volker Grewe, Johannes Hendricks, Patrick Jöckel, Anna Lanteri, Sigrun Matthes, Vanessa S. Rieger, Mattia Righi, and Robin N. Thor
Atmos. Chem. Phys., 24, 12079–12106, https://doi.org/10.5194/acp-24-12079-2024, https://doi.org/10.5194/acp-24-12079-2024, 2024
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We quantified the contributions of land transport, shipping, and aviation emissions to tropospheric ozone; its radiative forcing; and the reductions of the methane lifetime using chemistry-climate model simulations. The contributions were analysed for the conditions of 2015 and for three projections for the year 2050. The results highlight the challenges of mitigating ozone formed by emissions of the transport sector, caused by the non-linearitiy of the ozone chemistry and the long lifetime.
Lauri Franzon, Marie Camredon, Richard Valorso, Bernard Aumont, and Theo Kurtén
Atmos. Chem. Phys., 24, 11679–11699, https://doi.org/10.5194/acp-24-11679-2024, https://doi.org/10.5194/acp-24-11679-2024, 2024
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In this article we investigate the formation of large, sticky molecules from various organic compounds entering the atmosphere as primary emissions and the degree to which these processes may contribute to organic aerosol particle mass. More specifically, we qualitatively investigate a recently discovered chemical reaction channel for one of the most important short-lived radical compounds, peroxy radicals, and discover which of these reactions are most atmospherically important.
Siting Li, Yiming Liu, Yuqi Zhu, Yinbao Jin, Yingying Hong, Ao Shen, Yifei Xu, Haofan Wang, Haichao Wang, Xiao Lu, Shaojia Fan, and Qi Fan
Atmos. Chem. Phys., 24, 11521–11544, https://doi.org/10.5194/acp-24-11521-2024, https://doi.org/10.5194/acp-24-11521-2024, 2024
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This study establishes an inventory of anthropogenic chlorine emissions in China in 2019 with expanded species (HCl, Cl-, Cl2, HOCl) and sources (41 specific sources). The inventory is validated by a modeling study against the observations. This study enhances the understanding of anthropogenic chlorine emissions in the atmosphere, identifies key sources, and provides scientific support for pollution control and climate change.
Willem E. van Caspel, Zbigniew Klimont, Chris Heyes, and Hilde Fagerli
Atmos. Chem. Phys., 24, 11545–11563, https://doi.org/10.5194/acp-24-11545-2024, https://doi.org/10.5194/acp-24-11545-2024, 2024
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Methane in the atmosphere contributes to the production of ozone gas – an air pollutant and greenhouse gas. Our results highlight that simultaneous reductions in methane emissions help avoid offsetting the air pollution benefits already achieved by the already-approved precursor emission reductions by 2050 in the European Monitoring and Evaluation Programme region, while also playing an important role in bringing air pollution further down towards World Health Organization guideline limits.
Tia R. Scarpelli, Paul I. Palmer, Mark Lunt, Ingrid Super, and Arjan Droste
Atmos. Chem. Phys., 24, 10773–10791, https://doi.org/10.5194/acp-24-10773-2024, https://doi.org/10.5194/acp-24-10773-2024, 2024
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Under the Paris Agreement, countries must track their anthropogenic greenhouse gas emissions. This study describes a method to determine self-consistent estimates for combustion emissions and natural fluxes of CO2 from atmospheric data. We report consistent estimates inferred using this approach from satellite data and ground-based data over Europe, suggesting that satellite data can be used to determine national anthropogenic CO2 emissions for countries where ground-based CO2 data are absent.
Ryan J. Pound, Lucy V. Brown, Mat J. Evans, and Lucy J. Carpenter
Atmos. Chem. Phys., 24, 9899–9921, https://doi.org/10.5194/acp-24-9899-2024, https://doi.org/10.5194/acp-24-9899-2024, 2024
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Iodine-mediated loss of ozone to the ocean surface and the subsequent emission of iodine species has a large effect on the troposphere. Here we combine recent experimental insights to develop a box model of the process, which we then parameterize and incorporate into the GEOS-Chem transport model. We find that these new insights have a small impact on the total emission of iodine but significantly change its distribution.
Katherine R. Travis, Benjamin A. Nault, James H. Crawford, Kelvin H. Bates, Donald R. Blake, Ronald C. Cohen, Alan Fried, Samuel R. Hall, L. Gregory Huey, Young Ro Lee, Simone Meinardi, Kyung-Eun Min, Isobel J. Simpson, and Kirk Ullman
Atmos. Chem. Phys., 24, 9555–9572, https://doi.org/10.5194/acp-24-9555-2024, https://doi.org/10.5194/acp-24-9555-2024, 2024
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Human activities result in the emission of volatile organic compounds (VOCs) that contribute to air pollution. Detailed VOC measurements were taken during a field study in South Korea. When compared to VOC inventories, large discrepancies showed underestimates from chemical products, liquefied petroleum gas, and long-range transport. Improved emissions and chemistry of these VOCs better described urban pollution. The new chemical scheme is relevant to urban areas and other VOC sources.
Beth S. Nelson, Zhenze Liu, Freya A. Squires, Marvin Shaw, James R. Hopkins, Jacqueline F. Hamilton, Andrew R. Rickard, Alastair C. Lewis, Zongbo Shi, and James D. Lee
Atmos. Chem. Phys., 24, 9031–9044, https://doi.org/10.5194/acp-24-9031-2024, https://doi.org/10.5194/acp-24-9031-2024, 2024
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The impact of combined air quality and carbon neutrality policies on O3 formation in Beijing was investigated. Emissions inventory data were used to estimate future pollutant mixing ratios relative to ground-level observations. O3 production was found to be most sensitive to changes in alkenes, but large reductions in less reactive compounds led to larger reductions in future O3 production. This study highlights the importance of understanding the emissions of organic pollutants.
Takashi Sekiya, Emanuele Emili, Kazuyuki Miyazaki, Antje Inness, Zhen Qu, R. Bradley Pierce, Dylan Jones, Helen Worden, William Y. Y. Cheng, Vincent Huijnen, and Gerbrand Koren
EGUsphere, https://doi.org/10.5194/egusphere-2024-2426, https://doi.org/10.5194/egusphere-2024-2426, 2024
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Five global chemical reanalysis datasets were used to assess the relative impacts of assimilating satellite ozone and its precursors measurements on tropospheric ozone analyses for 2010. The multiple reanalysis system comparison allows for evaluating dependency of the impacts on different reanalysis systems. The results suggested the importance of satellite ozone and its precursor measurements for improving ozone analysis in the whole troposphere, with varying the magnitudes among the systems.
Maureen Beaudor, Didier Hauglustaine, Juliette Lathière, Martin Van Damme, Lieven Clarisse, and Nicolas Vuichard
EGUsphere, https://doi.org/10.5194/egusphere-2024-2022, https://doi.org/10.5194/egusphere-2024-2022, 2024
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Agriculture is the biggest ammonia (NH3) source, impacting air quality, climate, and ecosystems. Because of food demand, NH3 emissions are projected to rise by 2100. Using a global model, we analyzed the impact of present and future NH3 emissions generated from a land model. Our results show improved ammonia patterns compared to a reference inventory. Future scenarios predict up to 70 % increase in global NH3 burden, significant changes in radiative forcing, and could significantly elevate N2O.
Amir H. Souri, Bryan N. Duncan, Sarah A. Strode, Daniel C. Anderson, Michael E. Manyin, Junhua Liu, Luke D. Oman, Zhen Zhang, and Brad Weir
Atmos. Chem. Phys., 24, 8677–8701, https://doi.org/10.5194/acp-24-8677-2024, https://doi.org/10.5194/acp-24-8677-2024, 2024
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We explore a new method of using the wealth of information obtained from satellite observations of Aura OMI NO2, HCHO, and MERRA-2 reanalysis in NASA’s GEOS model equipped with an efficient tropospheric OH (TOH) estimator to enhance the representation of TOH spatial distribution and its long-term trends. This new framework helps us pinpoint regional inaccuracies in TOH and differentiate between established prior knowledge and newly acquired information from satellites on TOH trends.
Haipeng Lin, Louisa K. Emmons, Elizabeth W. Lundgren, Laura Hyesung Yang, Xu Feng, Ruijun Dang, Shixian Zhai, Yunxiao Tang, Makoto M. Kelp, Nadia K. Colombi, Sebastian D. Eastham, Thibaud M. Fritz, and Daniel J. Jacob
Atmos. Chem. Phys., 24, 8607–8624, https://doi.org/10.5194/acp-24-8607-2024, https://doi.org/10.5194/acp-24-8607-2024, 2024
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Tropospheric ozone is a major air pollutant, a greenhouse gas, and a major indicator of model skill. Global atmospheric chemistry models show large differences in simulations of tropospheric ozone, but isolating sources of differences is complicated by different model environments. By implementing the GEOS-Chem model side by side to CAM-chem within a common Earth system model, we identify and evaluate specific differences between the two models and their impacts on key chemical species.
Victor Lannuque and Karine Sartelet
Atmos. Chem. Phys., 24, 8589–8606, https://doi.org/10.5194/acp-24-8589-2024, https://doi.org/10.5194/acp-24-8589-2024, 2024
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Large uncertainties remain in understanding secondary organic aerosol (SOA) formation and speciation from naphthalene oxidation. This study details the development of the first near-explicit chemical scheme for naphthalene oxidation by OH, which includes kinetic and mechanistic data, and is able to reproduce most of the experimentally identified products in both gas and particle phases.
Hui Li, Jiaxin Qiu, and Bo Zheng
EGUsphere, https://doi.org/10.5194/egusphere-2024-1986, https://doi.org/10.5194/egusphere-2024-1986, 2024
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We conduct a sensitivity analysis on various factors including prior, model resolution, satellite constraint, and inversion system configuration to assess the vulnerability of emission estimates across temporal, sectoral, and regional dimensions. Our analysis first reveals the robustness of emissions estimated by this air pollution satellite sensor-based CO2 emission inversion system, with relative change between tests and Base inversion below 4.0 % for national annual NOx and CO2 emissions.
Shuai Li, Xiao Lu, and Haolin Wang
EGUsphere, https://doi.org/10.5194/egusphere-2024-1889, https://doi.org/10.5194/egusphere-2024-1889, 2024
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We report that the summertime ozone-temperature sensitivity decreased by 50 % from 3.0 ppbv/K in 1990 to 1.5 ppb/K in 2021 in the US. GEOS-Chem simulations show that anthropogenic NOx emission reduction is the dominant driver of the ozone-temperature sensitivity decline, through influencing both the temperature-direct and temperature-indirect processes. Reduced ozone-temperature sensitivity has decreased the ozone enhancement from low to high temperatures by an average of 6.8 ppbv across the US.
Tong Sha, Siyu Yang, Qingcai Chen, Liangqing Li, Xiaoyan Ma, Yan-Lin Zhang, Zhaozhong Feng, K. Folkert Boersma, and Jun Wang
Atmos. Chem. Phys., 24, 8441–8455, https://doi.org/10.5194/acp-24-8441-2024, https://doi.org/10.5194/acp-24-8441-2024, 2024
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Using an updated soil reactive nitrogen emission scheme in the Unified Inputs for Weather Research and Forecasting coupled with Chemistry (UI-WRF-Chem) model, we investigate the role of soil NO and HONO (Nr) emissions in air quality and temperature in North China. Contributions of soil Nr emissions to O3 and secondary pollutants are revealed, exceeding effects of soil NOx or HONO emission. Soil Nr emissions play an important role in mitigating O3 pollution and addressing climate change.
Jian Zhu, Shanshan Wang, Chuanqi Gu, Zhiwen Jiang, Sanbao Zhang, Ruibin Xue, Yuhao Yan, and Bin Zhou
Atmos. Chem. Phys., 24, 8383–8395, https://doi.org/10.5194/acp-24-8383-2024, https://doi.org/10.5194/acp-24-8383-2024, 2024
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In 2022, Shanghai implemented city-wide static management measures during the high-ozone season in April and May, providing a chance to study ozone pollution control. Despite significant emissions reductions, ozone levels increased by 23 %. Statistically, the number of days with higher ozone diurnal variation types increased during the lockdown period. The uneven decline in VOC and NO2 emissions led to heightened photochemical processes, resulting in the observed ozone level rise.
Hiroo Hata, Norifumi Mizushima, and Tomohiko Ihara
EGUsphere, https://doi.org/10.5194/egusphere-2024-1961, https://doi.org/10.5194/egusphere-2024-1961, 2024
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The introduction of battery electric vehicles (BEV) is expected to reduce the primary air pollutants from vehicular exhaust and evaporative emissions while reducing the anthropogenic heat produced by vehicles, ultimately decreasing the urban heat island effect (UHI). This study revealed the impact of introducing BEVs on the decrease in UHI and the effects of BEVs on the formation of tropospheric ozone and fine particulate matter in the Greater Tokyo Area of Japan.
Matthew J. Rowlinson, Mat J. Evans, Lucy J. Carpenter, Katie A. Read, Shalini Punjabi, Adedayo Adedeji, Luke Fakes, Ally Lewis, Ben Richmond, Neil Passant, Tim Murrells, Barron Henderson, Kelvin H. Bates, and Detlev Helmig
Atmos. Chem. Phys., 24, 8317–8342, https://doi.org/10.5194/acp-24-8317-2024, https://doi.org/10.5194/acp-24-8317-2024, 2024
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Ethane and propane are volatile organic compounds emitted from human activities which help to form ozone, a pollutant and greenhouse gas, and also affect the chemistry of the lower atmosphere. Atmospheric models tend to do a poor job of reproducing the abundance of these compounds in the atmosphere. By using regional estimates of their emissions, rather than globally consistent estimates, we can significantly improve the simulation of ethane in the model and make some improvement for propane.
Rodrigo J. Seguel, Lucas Castillo, Charlie Opazo, Néstor Y. Rojas, Thiago Nogueira, María Cazorla, Mario Gavidia-Calderón, Laura Gallardo, René Garreaud, Tomás Carrasco-Escaff, and Yasin Elshorbany
Atmos. Chem. Phys., 24, 8225–8242, https://doi.org/10.5194/acp-24-8225-2024, https://doi.org/10.5194/acp-24-8225-2024, 2024
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Trends of surface ozone were examined across South America. Our findings indicate that ozone trends in major South American cities either increase or remain steady, with no signs of decline. The upward trends can be attributed to chemical regimes that efficiently convert nitric oxide into nitrogen dioxide. Additionally, our results suggest a climate penalty for ozone driven by meteorological conditions that favor wildfire propagation in Chile and extensive heat waves in southern Brazil.
Maarten Krol, Bart van Stratum, Isidora Anglou, and Klaas Folkert Boersma
Atmos. Chem. Phys., 24, 8243–8262, https://doi.org/10.5194/acp-24-8243-2024, https://doi.org/10.5194/acp-24-8243-2024, 2024
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This paper presents detailed plume simulations of nitrogen oxides and carbon dioxide that are emitted from four large industrial facilities world-wide. Results from the high-resolution simulations that include atmospheric chemistry are compared to nitrogen dioxide observations from satellites. We find good performance of the model and show that common assumptions that are used in simplified models need revision. This work is important for the monitoring of emissions using satellite data.
Robin Plauchu, Audrey Fortems-Cheiney, Grégoire Broquet, Isabelle Pison, Antoine Berchet, Elise Potier, Gaëlle Dufour, Adriana Coman, Dilek Savas, Guillaume Siour, and Henk Eskes
Atmos. Chem. Phys., 24, 8139–8163, https://doi.org/10.5194/acp-24-8139-2024, https://doi.org/10.5194/acp-24-8139-2024, 2024
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This study uses the Community Inversion Framework and CHIMERE model to assess the potential of TROPOMI-S5P PAL NO2 tropospheric column data to estimate NOx emissions in France (2019–2021). Results show a 3 % decrease in average emissions compared to the 2016 CAMS-REG/INS, lower than the 14 % decrease from CITEPA. The study highlights challenges in capturing emission anomalies due to limited data coverage and error levels but shows promise for local inventory improvements.
Chelsea E. Stockwell, Matthew M. Coggon, Rebecca H. Schwantes, Colin Harkins, Bert Verreyken, Congmeng Lyu, Qindan Zhu, Lu Xu, Jessica B. Gilman, Aaron Lamplugh, Jeff Peischl, Michael A. Robinson, Patrick R. Veres, Meng Li, Andrew W. Rollins, Kristen Zuraski, Sunil Baidar, Shang Liu, Toshihiro Kuwayama, Steven S. Brown, Brian C. McDonald, and Carsten Warneke
EGUsphere, https://doi.org/10.5194/egusphere-2024-1899, https://doi.org/10.5194/egusphere-2024-1899, 2024
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In urban areas, emissions from everyday products like paints, cleaners, and personal care products, along with non-traditional sources such as cooking are important sources that impact air quality. This study used a model to evaluate how these emissions impact ozone in the Los Angeles Basin, and quantifies the impact of gaseous cooking emissions for the first time. Accurate representation of these and other man-made sources in inventories is crucial to inform effective air quality policies.
Zhendong Lu, Jun Wang, Yi Wang, Daven K. Henze, Xi Chen, Tong Sha, and Kang Sun
Atmos. Chem. Phys., 24, 7793–7813, https://doi.org/10.5194/acp-24-7793-2024, https://doi.org/10.5194/acp-24-7793-2024, 2024
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In contrast with past work showing that the reduction of emissions was the dominant factor for the nationwide increase of surface O3 during the lockdown in China, this study finds that the variation in meteorology (temperature and other parameters) plays a more important role. This result is obtained through sensitivity simulations using a chemical transport model constrained by satellite (TROPOMI) data and calibrated with surface observations.
Xiaohong Yao and Leiming Zhang
Atmos. Chem. Phys., 24, 7773–7791, https://doi.org/10.5194/acp-24-7773-2024, https://doi.org/10.5194/acp-24-7773-2024, 2024
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This study investigates long-term trends of criteria air pollutants, including NO2, CO, SO2, O3 and PM2.5, and NO2+O3 measured in 10 Canadian cities during the last 2 to 3 decades. We also investigate associated driving forces in terms of emission reductions, perturbations from varying weather conditions and large-scale wildfires, as well as changes in O3 sources and sinks.
Yao Ge, Sverre Solberg, Mathew R. Heal, Stefan Reimann, Willem van Caspel, Bryan Hellack, Thérèse Salameh, and David Simpson
Atmos. Chem. Phys., 24, 7699–7729, https://doi.org/10.5194/acp-24-7699-2024, https://doi.org/10.5194/acp-24-7699-2024, 2024
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Atmospheric volatile organic compounds (VOCs) constitute many species, acting as precursors to ozone and aerosol. Given the uncertainties in VOC emissions, lack of evaluation studies, and recent changes in emissions, this work adapts the EMEP MSC-W to evaluate emission inventories in Europe. We focus on the varying agreement between modelled and measured VOCs across different species and underscore potential inaccuracies in total and sector-specific emission estimates.
Shuzhuang Feng, Fei Jiang, Tianlu Qian, Nan Wang, Mengwei Jia, Songci Zheng, Jiansong Chen, Fang Ying, and Weimin Ju
Atmos. Chem. Phys., 24, 7481–7498, https://doi.org/10.5194/acp-24-7481-2024, https://doi.org/10.5194/acp-24-7481-2024, 2024
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We developed a multi-air-pollutant inversion system to estimate non-methane volatile organic compound (NMVOC) emissions using TROPOMI formaldehyde retrievals. We found that the inversion significantly improved formaldehyde simulations and reduced NMVOC emission uncertainties. The optimized NMVOC emissions effectively corrected the overestimation of O3 levels, mainly by decreasing the rate of the RO2 + NO reaction and increasing the rate of the NO2 + OH reaction.
Yuqing Qiu, Xin Li, Wenxuan Chai, Yi Liu, Mengdi Song, Xudong Tian, Qiaoli Zou, Wenjun Lou, Wangyao Zhang, Juan Li, and Yuanhang Zhang
EGUsphere, https://doi.org/10.5194/egusphere-2024-1576, https://doi.org/10.5194/egusphere-2024-1576, 2024
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The chemical reactions of ozone (O3) formation are related to meteorology and local emissions. Here, a random forest approach was used to eliminate the effects of meteorological factors (dispersion or transport) on O3 and its precursors. Variations in the sensitivity of O3 formation and the apportionment of emission sources were revealed after meteorological normalization. Our results suggest that meteorological variations should be considered when diagnosing O3 formation.
Haklim Choi, Alison L. Redington, Hyeri Park, Jooil Kim, Rona L. Thompson, Jens Mühle, Peter K. Salameh, Christina M. Harth, Ray F. Weiss, Alistair J. Manning, and Sunyoung Park
Atmos. Chem. Phys., 24, 7309–7330, https://doi.org/10.5194/acp-24-7309-2024, https://doi.org/10.5194/acp-24-7309-2024, 2024
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We analyzed with an inversion model the atmospheric abundance of hydrofluorocarbons (HFCs), potent greenhouse gases, from 2008 to 2020 at Gosan station in South Korea and revealed a significant increase in emissions, especially from eastern China and Japan. This increase contradicts reported data, underscoring the need for accurate monitoring and reporting. Our findings are crucial for understanding and managing global HFCs emissions, highlighting the importance of efforts to reduce HFCs.
Laura Hyesung Yang, Daniel J. Jacob, Ruijun Dang, Yujin J. Oak, Haipeng Lin, Jhoon Kim, Shixian Zhai, Nadia K. Colombi, Drew C. Pendergrass, Ellie Beaudry, Viral Shah, Xu Feng, Robert M. Yantosca, Heesung Chong, Junsung Park, Hanlim Lee, Won-Jin Lee, Soontae Kim, Eunhye Kim, Katherine R. Travis, James H. Crawford, and Hong Liao
Atmos. Chem. Phys., 24, 7027–7039, https://doi.org/10.5194/acp-24-7027-2024, https://doi.org/10.5194/acp-24-7027-2024, 2024
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The Geostationary Environment Monitoring Spectrometer (GEMS) provides hourly measurements of NO2. We use the chemical transport model to find how emissions, chemistry, and transport drive the changes in NO2 observed by GEMS at different times of the day. In winter, the chemistry plays a minor role, and high daytime emissions dominate the diurnal variation in NO2, balanced by transport. In summer, emissions, chemistry, and transport play an important role in shaping the diurnal variation in NO2.
M. Omar Nawaz, Jeremiah Johnson, Greg Yarwood, Benjamin de Foy, Laura Judd, and Daniel L. Goldberg
Atmos. Chem. Phys., 24, 6719–6741, https://doi.org/10.5194/acp-24-6719-2024, https://doi.org/10.5194/acp-24-6719-2024, 2024
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NO2 is a gas with implications for air pollution. A campaign conducted in Houston provided an opportunity to compare NO2 from different instruments and a model. Aircraft and satellite observations agreed well with measurements on the ground; however, the latter estimated lower values. We find that model-simulated NO2 was lower than observations, especially downtown, suggesting that NO2 sources associated with the urban core of Houston, such as vehicle emissions, may be underestimated.
Natalie Brett, Kathy S. Law, Steve R. Arnold, Javier G. Fochesatto, Jean-Christophe Raut, Tatsuo Onishi, Robert Gilliam, Kathleen Fahey, Deanna Huff, George Pouliot, Brice Barret, Elsa Dieudonne, Roman Pohorsky, Julia Schmale, Andrea Baccarini, Slimane Bekki, Gianluca Pappaccogli, Federico Scoto, Stefano Decesari, Antonio Donateo, Meeta Cesler-Maloney, William Simpson, Patrice Medina, Barbara D'Anna, Brice Temime-Roussel, Joel Savarino, Sarah Albertin, Jingqiu Mao, Becky Alexander, Allison Moon, Peter F. DeCarlo, Vanessa Selimovic, Robert Yokelson, and Ellis S. Robinson
EGUsphere, https://doi.org/10.5194/egusphere-2024-1450, https://doi.org/10.5194/egusphere-2024-1450, 2024
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Processes influencing dispersion of local anthropogenic emissions in Arctic wintertime are investigated with dispersion model simulations. Modelled power plant plume rise that considers surface and elevated temperature inversions improves results compared to observations. Modelled near-surface concentrations are improved by representation of vertical mixing and emission estimates. Large increases in diesel vehicle emissions at temperatures reaching -35 °C are required to reproduce observed NOx.
Tianlang Zhao, Jingqiu Mao, Zolal Ayazpour, Gonzalo González Abad, Caroline R. Nowlan, and Yiqi Zheng
Atmos. Chem. Phys., 24, 6105–6121, https://doi.org/10.5194/acp-24-6105-2024, https://doi.org/10.5194/acp-24-6105-2024, 2024
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HCHO variability is a key tracer in understanding VOC emissions in response to climate change. We investigate the role of methane oxidation and biogenic and wildfire emissions in HCHO interannual variability over northern high latitudes in summer, emphasizing wildfires as a key driver of HCHO interannual variability in Alaska, Siberia and northern Canada using satellite HCHO and SIF retrievals and then GEOS-Chem model. We show SIF is a tool to understand biogenic HCHO variability in this region.
Jianghao Li, Alastair C. Lewis, Jim R. Hopkins, Stephen J. Andrews, Tim Murrells, Neil Passant, Ben Richmond, Siqi Hou, William J. Bloss, Roy M. Harrison, and Zongbo Shi
Atmos. Chem. Phys., 24, 6219–6231, https://doi.org/10.5194/acp-24-6219-2024, https://doi.org/10.5194/acp-24-6219-2024, 2024
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A summertime ozone event at an urban site in Birmingham is sensitive to volatile organic compounds (VOCs) – particularly those of oxygenated VOCs. The roles of anthropogenic VOC sources in urban ozone chemistry are examined by integrating the 1990–2019 national atmospheric emission inventory into model scenarios. Road transport remains the most powerful means of further reducing ozone in this case study, but the benefits may be offset if solvent emissions of VOCs continue to increase.
Kai-Lan Chang, Owen R. Cooper, Audrey Gaudel, Irina Petropavlovskikh, Peter Effertz, Gary Morris, and Brian C. McDonald
Atmos. Chem. Phys., 24, 6197–6218, https://doi.org/10.5194/acp-24-6197-2024, https://doi.org/10.5194/acp-24-6197-2024, 2024
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A great majority of observational trend studies of free tropospheric ozone use sparsely sampled ozonesonde and aircraft measurements as reference data sets. A ubiquitous assumption is that trends are accurate and reliable so long as long-term records are available. We show that sampling bias due to sparse samples can persistently reduce the trend accuracy, and we highlight the importance of maintaining adequate frequency and continuity of observations.
Jin Ma, Linda M. J. Kooijmans, Norbert Glatthor, Stephen A. Montzka, Marc von Hobe, Thomas Röckmann, and Maarten C. Krol
Atmos. Chem. Phys., 24, 6047–6070, https://doi.org/10.5194/acp-24-6047-2024, https://doi.org/10.5194/acp-24-6047-2024, 2024
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The global budget of atmospheric COS can be optimised by inverse modelling using TM5-4DVAR, with the co-constraints of NOAA surface observations and MIPAS satellite data. We found reduced COS biosphere uptake from inversions and improved land and ocean separation using MIPAS satellite data assimilation. Further improvements are expected from better quantification of COS ocean and biosphere fluxes.
Cited articles
Aiuppa, A., Bellomo, S., D'Alessandro, W., Federico, C., Ferm, M., and Valenza,
M.: Volcanic plume monitoring at Mount Etna by diffusive (passive) sampling,
J. Geophys. Res.-Atmos., 109, D21308,
https://doi.org/10.1029/2003JD004481, 2004. a
Aiuppa, A., Federico, C., Franco, A., Giudice, G., Gurrieri, S., Inguaggiato,
S., Liuzzo, M., McGonigle, A. J. S., and Valenza, M.: Emission of bromine and
iodine from Mount Etna volcano, Geochem. Geophy. Geosy., 6, Q08008,
https://doi.org/10.1029/2005gc000965, 2005. a, b
Aiuppa, A., Franco, A., von Glasow, R., Allen, A. G., D'Alessandro, W., Mather, T. A., Pyle, D. M., and Valenza, M.: The tropospheric processing of acidic gases and hydrogen sulphide in volcanic gas plumes as inferred from field and model investigations, Atmos. Chem. Phys., 7, 1441–1450, https://doi.org/10.5194/acp-7-1441-2007, 2007. a
Aiuppa, A., Giudice, G., Gurrieri, S., Liuzzo, M., Burton, M., Caltabiano, T.,
McGonigle, A. J. S., Salerno, G., Shinohara, H., and Valenza, M.: Total
volatile flux from Mount Etna, Geophys. Res. Lett., 35, L24302,
https://doi.org/10.1029/2008GL035871, 2008. a
Ammann, M., Cox, R. A., Crowley, J. N., Jenkin, M. E., Mellouki, A., Rossi, M. J., Troe, J., and Wallington, T. J.: Evaluated kinetic and photochemical data for atmospheric chemistry: Volume VI – heterogeneous reactions with liquid substrates, Atmos. Chem. Phys., 13, 8045–8228, https://doi.org/10.5194/acp-13-8045-2013, 2013. a
Badia, A., Reeves, C. E., Baker, A. R., Saiz-Lopez, A., Volkamer, R., Koenig, T. K., Apel, E. C., Hornbrook, R. S., Carpenter, L. J., Andrews, S. J., Sherwen, T., and von Glasow, R.: Importance of reactive halogens in the tropical marine atmosphere: a regional modelling study using WRF-Chem, Atmos. Chem. Phys., 19, 3161–3189, https://doi.org/10.5194/acp-19-3161-2019, 2019. a
Bagnato, E., Aiuppa, A., Parello, F., Calabrese, S., D’Alessandro, W., T.A.,
M., McGonigle, A., Pyle, D., and Wängberg, I.: Degassing of gaseous
(elemental and reactive) and particulate mercury from Mount Etna volcano
(Southern Italy), Atmos. Environ., 41, 7377–7388,
https://doi.org/10.1016/j.atmosenv.2007.05.060, 2007. a
Bagnato, E., Tamburello, G., Avard, G., Martinez Cruz, M., Enrico, M., Fu, X.,
Sprovieri, M., and Sonke, J.: Mercury fluxes from volcanic and geothermal
sources: An update, Geological Society London Special Publications, 410, p. 263,
https://doi.org/10.1144/SP410.2, 2014. a
Bekki, S.: Oxidation of volcanic SO2: A sink for stratospheric OH and H2O,
Geophys. Res. Lett., 22, 913–916, https://doi.org/10.1029/95gl00534, 1995. a
Bobrowski, N. and Giuffrida, G.: Bromine monoxide / sulphur dioxide ratios in relation to volcanological observations at Mt. Etna 2006–2009, Solid Earth, 3, 433–445, https://doi.org/10.5194/se-3-433-2012, 2012. a
Bobrowski, N., Hönninger, G., Galle, B., and Platt, U.: Detection of
bromine monoxide in a volcanic plume, Nature, 423, 273–276,
https://doi.org/10.1038/nature01625, 2003. a
Bobrowski, N., von Glasow, R., Giuffrida, G. B., Tedesco, D., Aiuppa, A.,
Yalire, M., Arellano, S., Johansson, M., and Galle, B.: Gas emission strength
and evolution of the molar ratio of BrO
Bobrowski, N., Giuffrida, G. B., Arellano, S., Yalire, M., Liotta, M., Brusca,
L., Calabrese, S., Scaglione, S., Rüdiger, J., Castro, J. M., Galle, B.,
and Tedesco, D.: Plume composition and volatile flux of Nyamulagira volcano,
Democratic Republic of Congo, during birth and evolution of the lava lake,
2014–2015, B. Volcanol., 79, 90, https://doi.org/10.1007/s00445-017-1174-0,
2017. a
Brenna, H., Kutterolf, S., Mills, M. J., and Krüger, K.: The potential impacts of a sulfur- and halogen-rich supereruption such as Los Chocoyos on the atmosphere and climate, Atmos. Chem. Phys., 20, 6521–6539, https://doi.org/10.5194/acp-20-6521-2020, 2020. a, b
Buchholz, R. R., Emmons, L. K., Tilmes, S., and The CESM2 Development Team:
CESM2.1/CAM-chem Instantaneous Output for Boundary Conditions – Subset used:
20∘ N–45∘ N, 5∘ E–45∘ E 2018-12-21–2018-12-29,
https://doi.org/10.5065/NMP7-EP60, 2019. a
Burton, R. R., Woodhouse, M. J., Gadian, A. M., and Mobbs, S. D.: The Use of a
Numerical Weather Prediction Model to Simulate Near-Field Volcanic Plumes,
Atmosphere, 11, 594, https://doi.org/10.3390/atmos11060594, 2020. a
Cadoux, A., Scaillet, B., Bekki, S., Oppenheimer, C., and Druitt, T. H.:
Stratospheric Ozone destruction by the Bronze-Age Minoan eruption (Santorini
Volcano, Greece), Sci. Rep.-UK, 5, 12243, https://doi.org/10.1038/srep12243, 2015. a
Carn, S., Clarisse, L., and Prata, A.: Multi-decadal satellite measurements of
global volcanic degassing, J. Volcanol. Geoth. Res.,
311, 99–134, https://doi.org/10.1016/j.jvolgeores.2016.01.002, 2016. a
Dinger, F., Bobrowski, N., Warnach, S., Bredemeyer, S., Hidalgo, S., Arellano, S., Galle, B., Platt, U., and Wagner, T.: Periodicity in the BrO
Dinger, F., Kleinbek, T., Dörner, S., Bobrowski, N., Platt, U., Wagner, T., Ibarra, M., and Espinoza, E.: SO2 and BrO emissions of Masaya volcano from 2014 to 2020, Atmos. Chem. Phys., 21, 9367–9404, https://doi.org/10.5194/acp-21-9367-2021, 2021. a, b
Egan, S. D., Stuefer, M., Webley, P. W., Lopez, T., Cahill, C. F., and Hirtl, M.: Modeling volcanic ash aggregation processes and related impacts on the April–May 2010 eruptions of Eyjafjallajökull volcano with WRF-Chem, Nat. Hazards Earth Syst. Sci., 20, 2721–2737, https://doi.org/10.5194/nhess-20-2721-2020, 2020. a
Emmons, L. K., Schwantes, R. H., Orlando, J. J., Tyndall, G., Kinnison, D.,
Lamarque, J.-F., Marsh, D., Mills, M. J., Tilmes, S., Bardeen, C., Buchholz,
R. R., Conley, A., Gettelman, A., Garcia, R., Simpson, I., Blake, D. R.,
Meinardi, S., and Pétron, G.: The Chemistry Mechanism in the Community Earth
System Model version 2 (CESM2), J. Adv. Model. Earth
Sy., 12, e2019MS001882, https://doi.org/10.1029/2019MS001882, 2020. a
Freitas, S. R., Longo, K. M., Alonso, M. F., Pirre, M., Marecal, V., Grell, G., Stockler, R., Mello, R. F., and Sánchez Gácita, M.: PREP-CHEM-SRC – 1.0: a preprocessor of trace gas and aerosol emission fields for regional and global atmospheric chemistry models, Geosci. Model Dev., 4, 419–433, https://doi.org/10.5194/gmd-4-419-2011, 2011. a
Galeazzo, T., Bekki, S., Martin, E., Savarino, J., and Arnold, S. R.: Photochemical box modelling of volcanic SO2 oxidation: isotopic constraints, Atmos. Chem. Phys., 18, 17909–17931, https://doi.org/10.5194/acp-18-17909-2018, 2018. a, b, c
General, S., Bobrowski, N., Pöhler, D., Weber, K., Fischer, C., and Platt, U.:
Airborne I-DOAS measurements at Mt. Etna: BrO and OClO evolution in
the plume, J. Volcanol. Geoth. Res.,
300, 175–186, https://doi.org/10.1016/j.jvolgeores.2014.05.012, 2015. a, b
Gerlach, T. M.: Volcanic sources of tropospheric ozone-depleting trace gases,
Geochem. Geophy. Geosy., 5, Q09007, https://doi.org/10.1029/2004gc000747, 2004. a
Gliß, J., Bobrowski, N., Vogel, L., Pöhler, D., and Platt, U.: OClO and BrO observations in the volcanic plume of Mt. Etna – implications on the chemistry of chlorine and bromine species in volcanic plumes, Atmos. Chem. Phys., 15, 5659–5681, https://doi.org/10.5194/acp-15-5659-2015, 2015. a, b, c, d
Grell, G. A., Peckham, S. E., Schmitz, R., McKeen, S. A., Frost, G., Skamarock,
W. C., and Eder, B.: Fully coupled “online” chemistry within the WRF
model, Atmos. Environ., 39, 6957–6975,
https://doi.org/10.1016/j.atmosenv.2005.04.027, 2005. a
Gutmann, A., Bobrowski, N., Roberts, T. J., Rüdiger, J., and Hoffmann, T.:
Advances in Bromine Speciation in Volcanic Plumes, Front. Earth
Sci., 6, 213, https://doi.org/10.3389/feart.2018.00213, 2018. a, b, c, d
Hirtl, M., Stuefer, M., Arnold, D., Grell, G., Maurer, C., Natali, S.,
Scherllin-Pirscher, B., and Webley, P.: The effects of simulating volcanic
aerosol radiative feedbacks with WRF-Chem during the Eyjafjallajökull
eruption, April and May 2010, Atmos. Environ., 198, 194–206,
https://doi.org/10.1016/j.atmosenv.2018.10.058, 2019. a
Hirtl, M., Scherllin-Pirscher, B., Stuefer, M., Arnold, D., Baro, R., Maurer, C., and Mulder, M. D.: Extension of the WRF-Chem volcanic emission preprocessor to integrate complex source terms and evaluation for different emission scenarios of the Grimsvötn 2011 eruption, Nat. Hazards Earth Syst. Sci., 20, 3099–3115, https://doi.org/10.5194/nhess-20-3099-2020, 2020. a, b
Hörmann, C., Sihler, H., Bobrowski, N., Beirle, S., Penning de Vries, M., Platt, U., and Wagner, T.: Systematic investigation of bromine monoxide in volcanic plumes from space by using the GOME-2 instrument, Atmos. Chem. Phys., 13, 4749–4781, https://doi.org/10.5194/acp-13-4749-2013, 2013. a, b
Kelly, P. J., Kern, C., Roberts, T. J., Lopez, T., Werner, C., and Aiuppa, A.:
Rapid chemical evolution of tropospheric volcanic emissions from Redoubt
Volcano, Alaska, based on observations of ozone and halogen-containing gases,
J. Volcanol. Geoth. Res., 259, 317–333,
https://doi.org/10.1016/j.jvolgeores.2012.04.023, 2013. a, b, c, d, e
Klobas, J. E., Wilmouth, D. M., Weisenstein, D. K., Anderson, J. G., and
Salawitch, R. J.: Ozone depletion following future volcanic eruptions,
Geophys. Res. Lett., 44, 7490–7499, https://doi.org/10.1002/2017GL073972,
2017. a
Kutterolf, S., Hansteen, T., Appel, K., Freundt, A., Krg̈er, K., Pérez, W.,
and Wehrmann, H.: Combined bromine and chlorine release from large explosive
volcanic eruptions: A threat to stratospheric ozone?, Geology, 41, 707–710,
https://doi.org/10.1130/G34044.1, 2013. a
Lachatre, M., Mailler, S., Menut, L., Turquety, S., Sellitto, P., Guermazi, H., Salerno, G., Caltabiano, T., and Carboni, E.: New strategies for vertical transport in chemistry transport models: application to the case of the Mount Etna eruption on 18 March 2012 with CHIMERE v2017r4, Geosci. Model Dev., 13, 5707–5723, https://doi.org/10.5194/gmd-13-5707-2020, 2020. a
Lurton, T., Jégou, F., Berthet, G., Renard, J.-B., Clarisse, L., Schmidt, A., Brogniez, C., and Roberts, T. J.: Model simulations of the chemical and aerosol microphysical evolution of the Sarychev Peak 2009 eruption cloud compared to in situ and satellite observations, Atmos. Chem. Phys., 18, 3223–3247, https://doi.org/10.5194/acp-18-3223-2018, 2018. a, b
Marelle, L., Thomas, J. L., Ahmed, S., Tuite, K., Stutz, J., Dommergue, A.,
Simpson, W. R., Frey, M. M., and Baladima, F.: Implementation and impacts of
surface and blowing snow sources of Arctic bromine activation within WRF-Chem
4.1.1, J. Adv. Model. Earth Sy., 13, e2020MS002391,
https://doi.org/10.1029/2020MS002391, 2021. a
Martin, R. S., Ilyinskaya, E., and Oppenheimer, C.: The enigma of reactive
nitrogen in volcanic emissions, Geochim. Cosmochim. Ac., 95, 93–105,
https://doi.org/10.1016/j.gca.2012.07.027, 2012. a, b, c, d
Maters, E. C., Delmelle, P., Rossi, M. J., and Ayris, P. M.: Reactive Uptake of
Sulfur Dioxide and Ozone on Volcanic Glass and Ash at Ambient Temperature,
J. Geophys. Res.-Atmos., 122, 10,077–10,088,
https://doi.org/10.1002/2017JD026993, 2017. a
Mather, T., Allen, A., Davison, B., Pyle, D., Oppenheimer, C., and McGonigle,
A.: Nitric acid from volcanoes, Earth Planet. Sci. Lett., 218, 17–30, https://doi.org/10.1016/S0012-821X(03)00640-X, 2004a. a, b
Mather, T. A.: Volcanoes and the environment: Lessons for understanding Earth's
past and future from studies of present-day volcanic emissions, J.
Volcanol. Geoth. Res., 304, 160–179,
https://doi.org/10.1016/j.jvolgeores.2015.08.016, 2015. a
Mather, T. A., Pyle, D. M., and Allen, A. G.: Volcanic source for fixed
nitrogen in the early Earth's atmosphere, Geology, 32, 905–908,
https://doi.org/10.1130/G20679.1, 2004b. a
Millard, G. A., Mather, T. A., Pyle, D. M., Rose, W. I., and Thornton, B.:
Halogen emissions from a small volcanic eruption: Modeling the peak
concentrations, dispersion, and volcanically induced ozone loss in the
stratosphere, Geophys. Res. Lett., 33, L19815, https://doi.org/10.1029/2006GL026959,
2006. a
Ming, A., Winton, V. H. L., Keeble, J., Abraham, N. L., Dalvi, M. C.,
Griffiths, P., Caillon, N., Jones, A. E., Mulvaney, R., Savarino, J., Frey,
M. M., and Yang, X.: Stratospheric Ozone Changes From Explosive Tropical
Volcanoes: Modeling and Ice Core Constraints, J. Geophys. Res.-Atmos., 125, e2019JD032290, https://doi.org/10.1029/2019JD032290,
2020. a
National Centers for Environmental Prediction, National Weather Service,
NOAA, and U.S. Department of Commerce: NCEP FNL Operational Model Global
Tropospheric Analyses, continuing from July 1999,
https://doi.org/10.5065/D6M043C6, 2000. a
Oppenheimer, C., Kyle, P., Eisele, F., Crawford, J., Huey, G., Tanner, D., Kim,
S., Mauldin, L., Blake, D., Beyersdorf, A., Buhr, M., and Davis, D.:
Atmospheric chemistry of an Antarctic volcanic plume, J. Geophys.
Res.-Atmos., 115, D04303, https://doi.org/10.1029/2009jd011910, 2010. a
Oppenheimer, C., Scaillet, B., and Martin, R. S.: Sulfur Degassing From
Volcanoes: Source Conditions, Surveillance, Plume Chemistry and Earth System
Impacts, Reviews in Mineralogy and Geochemistry, 73, 363–421,
https://doi.org/10.2138/rmg.2011.73.13, 2011. a
Prata, A. J., Carn, S. A., Stohl, A., and Kerkmann, J.: Long range transport and fate of a stratospheric volcanic cloud from Soufrière Hills volcano, Montserrat, Atmos. Chem. Phys., 7, 5093–5103, https://doi.org/10.5194/acp-7-5093-2007, 2007. a
Pyle, D. and Mather, T.: Halogens in igneous processes and their fluxes to the
atmosphere and oceans from volcanic activity: A review, Chem. Geol.,
263, 110–121, https://doi.org/10.1016/j.chemgeo.2008.11.013, 2009. a
Pyle, D. M. and Mather, T. A.: The importance of volcanic emissions for the
global atmospheric mercury cycle, Atmos. Environ., 37, 5115–5124,
https://doi.org/10.1016/j.atmosenv.2003.07.011, 2003. a
Rizza, U., Brega, E., Caccamo, M. T., Castorina, G., Morichetti, M., Munaò,
G., Passerini, G., and Magazù, S.: Analysis of the ETNA 2015 Eruption Using
WRF–Chem Model and Satellite Observations, Atmosphere, 11, 1168,
https://doi.org/10.3390/atmos11111168, 2020. a
Roberts, T.: Ozone Depletion in Tropospheric Volcanic Plumes: From Halogen-Poor
to Halogen-Rich Emissions, Geosciences, 8, 68,
https://doi.org/10.3390/geosciences8020068, 2018. a, b
Roberts, T., Vignelles, D., Liuzzo, M., Giudice, G., Aiuppa, A., Coltelli, M.,
Salerno, G., Chartier, M., Couté, B., Berthet, G., Lurton, T., Dulac, F.,
and Renard, J.-B.: The primary volcanic aerosol emission from Mt Etna:
Size-resolved particles with SO2 and role in plume reactive halogen
chemistry, Geochim. Cosmochim. Ac., 222, 74–93,
https://doi.org/10.1016/j.gca.2017.09.040, 2018. a, b, c, d, e, f
Roberts, T., Dayma, G., and Oppenheimer, C.: Reaction Rates Control
High-Temperature Chemistry of Volcanic Gases in Air, Front. Earth
Sci., 7, 154, https://doi.org/10.3389/feart.2019.00154, 2019. a, b, c, d
Roberts, T. J., Braban, C. F., Martin, R. S., Oppenheimer, C., Adams, J. W.,
Cox, R. A., Jones, R. L., and Griffiths, P. T.: Modelling reactive halogen
formation and ozone depletion in volcanic plumes, Chem. Geol., 263,
151–163, https://doi.org/10.1016/j.chemgeo.2008.11.012, 2009. a, b, c
Roberts, T. J., Martin, R. S., and Jourdain, L.: Reactive bromine chemistry in Mount Etna's volcanic plume: the influence of total Br, high-temperature processing, aerosol loading and plume–air mixing, Atmos. Chem. Phys., 14, 11201–11219, https://doi.org/10.5194/acp-14-11201-2014, 2014. a, b, c, d, e
Rose, W. I., Millard, G. A., Mather, T. A., Hunton, D. E., Anderson, B.,
Oppenheimer, C., Thornton, B. F., Gerlach, T. M., Viggiano, A. A., Kondo, Y.,
Miller, T. M., and Ballenthin, J. O.: Atmospheric chemistry of a 33–34 hour
old volcanic cloud from Hekla Volcano (Iceland): Insights from direct
sampling and the application of chemical box modeling, J. Geophys.
Res., 111, D20206, https://doi.org/10.1029/2005jd006872, 2006. a, b, c
Rüdiger, J., Bobrowski, N., Liotta, M., and Hoffmann, T.: Development and
application of a sampling method for the determination of reactive halogen
species in volcanic gas emissions, Anal. Bioanal. Chem.,
409, 5975–5985, https://doi.org/10.1007/s00216-017-0525-1, 2017. a
Rüdiger, J., Gutmann, A., Bobrowski, N., Liotta, M., de Moor, J. M., Sander, R., Dinger, F., Tirpitz, J.-L., Ibarra, M., Saballos, A., Martínez, M., Mendoza, E., Ferrufino, A., Stix, J., Valdés, J., Castro, J. M., and Hoffmann, T.: Halogen activation in the plume of Masaya volcano: field observations and box model investigations, Atmos. Chem. Phys., 21, 3371–3393, https://doi.org/10.5194/acp-21-3371-2021, 2021. a, b, c, d
Saiz-Lopez, A., Sitkiewicz, S. P., Roca-Sanjuán, D., Oliva-Enrich, J. M.,
Dávalos, J. Z., Notario, R., Jiskra, M., Xu, Y., Wang, F., Thackray,
C. P., Sunderland, E. M., Jacob, D. J., Travnikov, O., Cuevas, C. A.,
Acuña, A. U., Rivero, D., Plane, J. M. C., Kinnison, D. E., and Sonke,
J. E.: Photoreduction of gaseous oxidized mercury changes global atmospheric
mercury speciation, transport and deposition, Nat. Commun., 9, 4796,
https://doi.org/10.1038/s41467-018-07075-3, 2018. a
Saiz-Lopez, A., Acuña, A. U., Trabelsi, T., Carmona-García, J., Dávalos,
J. Z., Rivero, D., Cuevas, C. A., Kinnison, D. E., Sitkiewicz, S. P.,
Roca-Sanjuán, D., and Francisco, J. S.: Gas-Phase Photolysis of Hg(I)
Radical Species: A New Atmospheric Mercury Reduction Process, J.
Am. Chem. Soc., 141, 8698–8702, https://doi.org/10.1021/jacs.9b02890, 2019. a, b, c
Salerno, G., Burton, M., Oppenheimer, C., Caltabiano, T., Randazzo, D., Bruno,
N., and Longo, V.: Three-years of SO2 flux measurements of Mt. Etna
using an automated UV scanner array: Comparison with conventional traverses
and uncertainties in flux retrieval, Journal of Volcanology and Geothermal
Research, 183, 76–83, https://doi.org/10.1016/j.jvolgeores.2009.02.013, 2009. a
Seigneur, C. and Lohman, K.: Effect of bromine chemistry on the atmospheric
mercury cycle, J. Geophys. Res.-Atmos., 113, D23309,
https://doi.org/10.1029/2008JD010262, 2008. a
Seigneur, C., Vijayaraghavan, K., and Lohman, K.: Atmospheric mercury
chemistry: Sensitivity of global model simulations to chemical reactions,
J. Geophys. Res., 111, D22306, https://doi.org/10.1029/2005jd006780,
2006. a
Seo, S., Richter, A., Blechschmidt, A.-M., Bougoudis, I., and Burrows, J. P.: First high-resolution BrO column retrievals from TROPOMI, Atmos. Meas. Tech., 12, 2913–2932, https://doi.org/10.5194/amt-12-2913-2019, 2019. a
Staunton-Sykes, J., Aubry, T. J., Shin, Y. M., Weber, J., Marshall, L. R., Luke Abraham, N., Archibald, A., and Schmidt, A.: Co-emission of volcanic sulfur and halogens amplifies volcanic effective radiative forcing, Atmos. Chem. Phys., 21, 9009–9029, https://doi.org/10.5194/acp-21-9009-2021, 2021. a
Stuefer, M., Freitas, S. R., Grell, G., Webley, P., Peckham, S., McKeen, S. A., and Egan, S. D.: Inclusion of ash and SO2 emissions from volcanic eruptions in WRF-Chem: development and some applications, Geosci. Model Dev., 6, 457–468, https://doi.org/10.5194/gmd-6-457-2013, 2013. a
Surl, L.: Modelling the atmospheric chemistry of volcanic plumes, PhD thesis,
University of East Anglia, available at:
https://ueaeprints.uea.ac.uk/id/eprint/59407/ (last access: 12 August 2021), 2016. a
Surl, L.: WRF-Chem Volcano, Github [software], available at: https://github.com/LukeSurl/WCV (last access: 12 August 2021),
2020. a
Surl, L.: WRF-Chem Volcano output – Etna Summer 2012, Zenodo [data set],
https://doi.org/10.5281/zenodo.4415788, 2021. a
Theys, N., Van Roozendael, M., Dils, B., Hendrick, F., Hao, N., and
De Mazière, M.: First satellite detection of volcanic bromine monoxide
emission after the Kasatochi eruption, Geophys. Res. Lett., 36, L03809,
https://doi.org/10.1029/2008GL036552, 2009. a
Theys, N., De Smedt, I., Van Roozendael, M., Froidevaux, L., Clarisse, L., and
Hendrick, F.: First satellite detection of volcanic OClO after the eruption
of Puyehue-Cordón Caulle, Geophys. Res. Lett., 41, 667–672,
https://doi.org/10.1002/2013GL058416, 2014. a
Vance, A., McGonigle, A. J. S., Aiuppa, A., Stith, J. L., Turnbull, K., and von
Glasow, R.: Ozone depletion in tropospheric volcanic plumes, Geophys.
Res. Lett., 37, L22802, https://doi.org/10.1029/2010GL044997, 2010. a, b
Voigt, C., Jessberger, P., Jurkat, T., Kaufmann, S., Baumann, R., Schlager, H.,
Bobrowski, N., Giuffrida, G., and Salerno, G.: Evolution of CO2, SO2,
HCl, and HNO3 in the volcanic plumes from Etna, Geophys. Res.
Lett., 41, 2196–2203, https://doi.org/10.1002/2013gl058974, 2014. a, b, c
von Glasow, R., Bobrowski, N., and Kern, C.: The effects of volcanic eruptions
on atmospheric chemistry, Chem. Geol., 263, 131–142,
https://doi.org/10.1016/j.chemgeo.2008.08.020, 2009. a
Wade, D. C., Vidal, C. M., Abraham, N. L., Dhomse, S., Griffiths, P. T.,
Keeble, J., Mann, G., Marshall, L., Schmidt, A., and Archibald, A. T.:
Reconciling the climate and ozone response to the 1257 CE Mount Samalas
eruption, P. Natl. Acad. Sci. USA, 117,
26651–26659, https://doi.org/10.1073/pnas.1919807117, 2020. a
Warnach, S., Bobrowski, N., Hidalgo, S., Arellano, S., Sihler, H., Dinger, F.,
Lübcke, P., Battaglia, J., Steele, A., Galle, B., Platt, U., and Wagner,
T.: Variation of the BrO/SO2 Molar Ratio in the Plume of Tungurahua
Volcano Between 2007 and 2017 and Its Relationship to Volcanic Activity,
Front. Earth Sci., 7, p. 132, https://doi.org/10.3389/feart.2019.00132, 2019. a, b
Weigelt, A., Ebinghaus, R., Pirrone, N., Bieser, J., Bödewadt, J., Esposito, G., Slemr, F., van Velthoven, P. F. J., Zahn, A., and Ziereis, H.: Tropospheric mercury vertical profiles between 500 and 10 000 m in central Europe, Atmos. Chem. Phys., 16, 4135–4146, https://doi.org/10.5194/acp-16-4135-2016, 2016a. a, b, c
Weigelt, A., Slemr, F., Ebinghaus, R., Pirrone, N., Bieser, J., Bödewadt, J., Esposito, G., and van Velthoven, P. F. J.: Mercury emissions of a coal-fired power plant in Germany, Atmos. Chem. Phys., 16, 13653–13668, https://doi.org/10.5194/acp-16-13653-2016, 2016b. a
Wennberg, P.: Atmospheric chemistry – Bromine explosion, Nature, 397, 299,
https://doi.org/10.1038/16805, 1999. a
Wild, O., Zhu, X., and Prather, M. J.: Fast-J: Accurate Simulation of In- and
Below-Cloud Photolysis in Tropospheric Chemical Models, J.
Atmos. Chem., 37, 245–282, https://doi.org/10.1023/a:1006415919030, 2000. a
Witt, M. L. I., Mather, T. A., Pyle, D. M., Aiuppa, A., Bagnato, E., and
Tsanev, V. I.: Mercury and halogen emissions from Masaya and Telica
volcanoes, Nicaragua, J. Geophys. Res.-Sol. Ea., 113, B06203,
https://doi.org/10.1029/2007JB005401, 2008. a
Wittmer, J., Bobrowski, N., Liotta, M., Giuffrida, G., Calabrese, S., and U.,
P.: Active alkaline traps to determine acidic-gas ratios in volcanic plumes:
sampling technique and analytical Methods, Geochem. Geophys. Geosys., 15, 2797–2820,
https://doi.org/10.1002/2013GC005133, 2014. a, b, c, d
Zaveri, R. A. and Peters, L. K.: A new lumped structure photochemical mechanism
for large-scale applications, J. Geophys. Res.-Atmos.,
104, 30387–30415, https://doi.org/10.1029/1999JD900876, 1999.
a
Zaveri, R. A., Easter, R. C., Fast, J. D., and Peters, L. K.: Model for
Simulating Aerosol Interactions and Chemistry (MOSAIC), J. Geophys. Res.-Atmos., 113, D13204, https://doi.org/10.1029/2007JD008782, 2008. a
Short summary
Many different chemical reactions happen when the gases from a volcano mix with air, but what effects do they have? We present aircraft measurements which show that there is less ozone within the plume of Etna than outside it. We have also made a computer model of this chemistry. This model can reproduce the effects seen when halogens (bromine and chlorine) are included in the volcanic emissions.
We look closely at the simulation to discover how complicated halogen reactions cause ozone loss.
Many different chemical reactions happen when the gases from a volcano mix with air, but what...
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