Articles | Volume 21, issue 17
https://doi.org/10.5194/acp-21-13287-2021
© 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-21-13287-2021
© Author(s) 2021. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Research article
| 
08 Sep 2021
Research article |
| 08 Sep 2021
| 08 Sep 2021
Dynamics of gaseous oxidized mercury at Villum Research Station during the High Arctic summer
Department of Environmental Science, iClimate, Arctic Research Center,
Aarhus University, Frederiksborgvej 399, 4000 Roskilde, Denmark
Bjarne Jensen
Department of Environmental Science, iClimate, Arctic Research Center,
Aarhus University, Frederiksborgvej 399, 4000 Roskilde, Denmark
Andreas Massling
Department of Environmental Science, iClimate, Arctic Research Center,
Aarhus University, Frederiksborgvej 399, 4000 Roskilde, Denmark
Daniel Charles Thomas
Department of Environmental Science, iClimate, Arctic Research Center,
Aarhus University, Frederiksborgvej 399, 4000 Roskilde, Denmark
Henrik Skov
Department of Environmental Science, iClimate, Arctic Research Center,
Aarhus University, Frederiksborgvej 399, 4000 Roskilde, Denmark
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Formation of new particles is a key process in the atmosphere. New particle formation events arising from nucleation of gaseous precursors have been analysed in extensive datasets from 13 sites in five European countries in terms of frequency, nucleation rate, and particle growth rate, with several common features and many differences identified. Although nucleation frequencies are lower at roadside sites, nucleation rates and particle growth rates are typically higher.
Ulas Im, Kostas Tsigaridis, Gregory Faluvegi, Peter L. Langen, Joshua P. French, Rashed Mahmood, Manu A. Thomas, Knut von Salzen, Daniel C. Thomas, Cynthia H. Whaley, Zbigniew Klimont, Henrik Skov, and Jørgen Brandt
Atmos. Chem. Phys., 21, 10413–10438, https://doi.org/10.5194/acp-21-10413-2021, https://doi.org/10.5194/acp-21-10413-2021, 2021
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Future (2015–2050) simulations of the aerosol burdens and their radiative forcing and climate impacts over the Arctic under various emission projections show that although the Arctic aerosol burdens are projected to decrease significantly by 10 to 60 %, regardless of the magnitude of aerosol reductions, surface air temperatures will continue to increase by 1.9–2.6 ℃, while sea-ice extent will continue to decrease, implying reductions of greenhouse gases are necessary to mitigate climate change.
Dimitrios Bousiotis, James Brean, Francis D. Pope, Manuel Dall'Osto, Xavier Querol, Andrés Alastuey, Noemi Perez, Tuukka Petäjä, Andreas Massling, Jacob Klenø Nøjgaard, Claus Nordstrøm, Giorgos Kouvarakis, Stergios Vratolis, Konstantinos Eleftheriadis, Jarkko V. Niemi, Harri Portin, Alfred Wiedensohler, Kay Weinhold, Maik Merkel, Thomas Tuch, and Roy M. Harrison
Atmos. Chem. Phys., 21, 3345–3370, https://doi.org/10.5194/acp-21-3345-2021, https://doi.org/10.5194/acp-21-3345-2021, 2021
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New particle formation events from 16 sites over Europe have been studied, and the influence of meteorological and atmospheric composition variables has been investigated. Some variables, like solar radiation intensity and temperature, have a positive effect on the occurrence of these events, while others have a negative effect, affecting different aspects such as the rate at which particles are formed or grow. This effect varies depending on the site type and magnitude of these variables.
Jakob B. Pernov, Rossana Bossi, Thibaut Lebourgeois, Jacob K. Nøjgaard, Rupert Holzinger, Jens L. Hjorth, and Henrik Skov
Atmos. Chem. Phys., 21, 2895–2916, https://doi.org/10.5194/acp-21-2895-2021, https://doi.org/10.5194/acp-21-2895-2021, 2021
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Volatile organic compounds (VOCs) are an important constituent in the Arctic atmosphere due to their effect on aerosol and ozone formation. However, an understanding of their sources is lacking. This research presents a multiseason high-time-resolution dataset of VOCs in the Arctic and details their temporal characteristics and source apportionment. Four sources were identified: biomass burning, marine cryosphere, background, and Arctic haze.
Xin Yang, Anne-M. Blechschmidt, Kristof Bognar, Audra McClure-Begley, Sara Morris, Irina Petropavlovskikh, Andreas Richter, Henrik Skov, Kimberly Strong, David W. Tarasick, Taneil Uttal, Mika Vestenius, and Xiaoyi Zhao
Atmos. Chem. Phys., 20, 15937–15967, https://doi.org/10.5194/acp-20-15937-2020, https://doi.org/10.5194/acp-20-15937-2020, 2020
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This is a modelling-based study on Arctic surface ozone, with a particular focus on spring ozone depletion events (i.e. with concentrations < 10 ppbv). Model experiments show that model runs with blowing-snow-sourced sea salt aerosols implemented as a source of reactive bromine can reproduce well large-scale ozone depletion events observed in the Arctic. This study supplies modelling evidence of the proposed mechanism of reactive-bromine release from blowing snow on sea ice (Yang et al., 2008).
Henrik Skov, Jens Hjorth, Claus Nordstrøm, Bjarne Jensen, Christel Christoffersen, Maria Bech Poulsen, Jesper Baldtzer Liisberg, David Beddows, Manuel Dall'Osto, and Jesper Heile Christensen
Atmos. Chem. Phys., 20, 13253–13265, https://doi.org/10.5194/acp-20-13253-2020, https://doi.org/10.5194/acp-20-13253-2020, 2020
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Mercury is toxic in all its forms. It bioaccumulates in food webs, is ubiquitous in the atmosphere, and atmospheric transport is an important source for this element in the Arctic. Measurements of gaseous elemental mercury have been carried out at the Villum Research Station at Station Nord in northern Greenland since 1999. The measurements are compared with model results from the Danish Eulerian Hemispheric Model. In this way, the dynamics of mercury are investigated.
Tuukka Petäjä, Ella-Maria Duplissy, Ksenia Tabakova, Julia Schmale, Barbara Altstädter, Gerard Ancellet, Mikhail Arshinov, Yurii Balin, Urs Baltensperger, Jens Bange, Alison Beamish, Boris Belan, Antoine Berchet, Rossana Bossi, Warren R. L. Cairns, Ralf Ebinghaus, Imad El Haddad, Beatriz Ferreira-Araujo, Anna Franck, Lin Huang, Antti Hyvärinen, Angelika Humbert, Athina-Cerise Kalogridis, Pavel Konstantinov, Astrid Lampert, Matthew MacLeod, Olivier Magand, Alexander Mahura, Louis Marelle, Vladimir Masloboev, Dmitri Moisseev, Vaios Moschos, Niklas Neckel, Tatsuo Onishi, Stefan Osterwalder, Aino Ovaska, Pauli Paasonen, Mikhail Panchenko, Fidel Pankratov, Jakob B. Pernov, Andreas Platis, Olga Popovicheva, Jean-Christophe Raut, Aurélie Riandet, Torsten Sachs, Rosamaria Salvatori, Roberto Salzano, Ludwig Schröder, Martin Schön, Vladimir Shevchenko, Henrik Skov, Jeroen E. Sonke, Andrea Spolaor, Vasileios K. Stathopoulos, Mikko Strahlendorff, Jennie L. Thomas, Vito Vitale, Sterios Vratolis, Carlo Barbante, Sabine Chabrillat, Aurélien Dommergue, Konstantinos Eleftheriadis, Jyri Heilimo, Kathy S. Law, Andreas Massling, Steffen M. Noe, Jean-Daniel Paris, André S. H. Prévôt, Ilona Riipinen, Birgit Wehner, Zhiyong Xie, and Hanna K. Lappalainen
Atmos. Chem. Phys., 20, 8551–8592, https://doi.org/10.5194/acp-20-8551-2020, https://doi.org/10.5194/acp-20-8551-2020, 2020
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The role of polar regions is increasing in terms of megatrends such as globalization, new transport routes, demography, and the use of natural resources with consequent effects on regional and transported pollutant concentrations. Here we summarize initial results from our integrative project exploring the Arctic environment and pollution to deliver data products, metrics, and indicators for stakeholders.
Jacob Schacht, Bernd Heinold, Johannes Quaas, John Backman, Ribu Cherian, Andre Ehrlich, Andreas Herber, Wan Ting Katty Huang, Yutaka Kondo, Andreas Massling, P. R. Sinha, Bernadett Weinzierl, Marco Zanatta, and Ina Tegen
Atmos. Chem. Phys., 19, 11159–11183, https://doi.org/10.5194/acp-19-11159-2019, https://doi.org/10.5194/acp-19-11159-2019, 2019
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The Arctic is warming faster than the rest of Earth. Black carbon (BC) aerosol contributes to this Arctic amplification by direct and indirect aerosol radiative effects while distributed in air or deposited on snow and ice. The aerosol-climate model ECHAM-HAM is used to estimate direct aerosol radiative effect (DRE). Airborne and near-surface BC measurements are used to evaluate the model and give an uncertainty range for the burden and DRE of Arctic BC caused by different emission inventories.
Ingeborg E. Nielsen, Henrik Skov, Andreas Massling, Axel C. Eriksson, Manuel Dall'Osto, Heikki Junninen, Nina Sarnela, Robert Lange, Sonya Collier, Qi Zhang, Christopher D. Cappa, and Jacob K. Nøjgaard
Atmos. Chem. Phys., 19, 10239–10256, https://doi.org/10.5194/acp-19-10239-2019, https://doi.org/10.5194/acp-19-10239-2019, 2019
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Measurements of the chemical composition of sub-micrometer aerosols were carried out in northern Greenland during the Arctic haze (February–May) where concentrations are high due to favorable conditions for long-range transport. Sulfate was the dominant aerosol (66 %), followed by organic matter (24 %). The highest black carbon concentrations where observed in February. Source apportionment yielded three factors: a primary factor (12 %), an Arctic haze factor (64 %) and a marine factor (22 %).
Manuel Dall'Osto, David C. S. Beddows, Peter Tunved, Roy M. Harrison, Angelo Lupi, Vito Vitale, Silvia Becagli, Rita Traversi, Ki-Tae Park, Young Jun Yoon, Andreas Massling, Henrik Skov, Robert Lange, Johan Strom, and Radovan Krejci
Atmos. Chem. Phys., 19, 7377–7395, https://doi.org/10.5194/acp-19-7377-2019, https://doi.org/10.5194/acp-19-7377-2019, 2019
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We present a cluster analysis of particle size distributions simultaneously collected from three European high Arctic sites centred in the Fram Strait during a 3-year period. Confined for longer time periods by consolidated pack sea ice regions, the Greenland site shows lower ultrafine-mode aerosol concentrations during summer relative to the Svalbard sites. Our study supports international environmental cooperation concerning the Arctic region.
Heike Wex, Lin Huang, Wendy Zhang, Hayley Hung, Rita Traversi, Silvia Becagli, Rebecca J. Sheesley, Claire E. Moffett, Tate E. Barrett, Rossana Bossi, Henrik Skov, Anja Hünerbein, Jasmin Lubitz, Mareike Löffler, Olivia Linke, Markus Hartmann, Paul Herenz, and Frank Stratmann
Atmos. Chem. Phys., 19, 5293–5311, https://doi.org/10.5194/acp-19-5293-2019, https://doi.org/10.5194/acp-19-5293-2019, 2019
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We found an annual cycle for ice-nucleating particles in the Arctic. These particles are important for Arctic clouds, as they can change the lifetime of clouds. We suggest that higher concentrations of these particles in summertime originate from the Arctic biosphere (both marine and terrestrial). With a warming Arctic, these concentrations may increase further, influencing aerosol–cloud interactions and therewith the observed strong warming of the Arctic.
Jesper Kamp, Henrik Skov, Bjarne Jensen, and Lise Lotte Sørensen
Atmos. Chem. Phys., 18, 6923–6938, https://doi.org/10.5194/acp-18-6923-2018, https://doi.org/10.5194/acp-18-6923-2018, 2018
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Measurements of mercury fluxes over snow surfaces are carried out at the High Arctic site at Villum Research Station in North Greenland. The measurements were carried out from 23 April to 12 May during spring 2016, where atmospheric mercury depletion events (AMDEs) took place. The measurements showed a net emission of 8.9 ng m−2 min−1, with only a few depositional fluxes. GEM fluxes and atmospheric temperature measurements suggest that GEM emission partly could be affected by surface heating.
Eyal Freud, Radovan Krejci, Peter Tunved, Richard Leaitch, Quynh T. Nguyen, Andreas Massling, Henrik Skov, and Leonard Barrie
Atmos. Chem. Phys., 17, 8101–8128, https://doi.org/10.5194/acp-17-8101-2017, https://doi.org/10.5194/acp-17-8101-2017, 2017
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This study analyses multi-year observations of atmospheric particles from five Arctic sites. These particles affect climate and air quality. The main factors that control the distinct annual cycle in the concentration of these particles are long-range transport and precipitation. The former brings pollution from the Asian sector – mostly during winter/spring – while the latter clears the air in summer/autumn. However, there are consistent differences between the sites due to regional factors.
Francesca Sprovieri, Nicola Pirrone, Mariantonia Bencardino, Francesco D'Amore, Francesco Carbone, Sergio Cinnirella, Valentino Mannarino, Matthew Landis, Ralf Ebinghaus, Andreas Weigelt, Ernst-Günther Brunke, Casper Labuschagne, Lynwill Martin, John Munthe, Ingvar Wängberg, Paulo Artaxo, Fernando Morais, Henrique de Melo Jorge Barbosa, Joel Brito, Warren Cairns, Carlo Barbante, María del Carmen Diéguez, Patricia Elizabeth Garcia, Aurélien Dommergue, Helene Angot, Olivier Magand, Henrik Skov, Milena Horvat, Jože Kotnik, Katie Alana Read, Luis Mendes Neves, Bernd Manfred Gawlik, Fabrizio Sena, Nikolay Mashyanov, Vladimir Obolkin, Dennis Wip, Xin Bin Feng, Hui Zhang, Xuewu Fu, Ramesh Ramachandran, Daniel Cossa, Joël Knoery, Nicolas Marusczak, Michelle Nerentorp, and Claus Norstrom
Atmos. Chem. Phys., 16, 11915–11935, https://doi.org/10.5194/acp-16-11915-2016, https://doi.org/10.5194/acp-16-11915-2016, 2016
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This work presents atmospheric Hg concentrations recorded within the GMOS global network analyzing Hg measurement results in terms of temporal trends, seasonality and comparability within the network. The over-arching benefit of this coordinated Hg monitoring network would clearly be the production of high-quality measurement datasets on a global scale useful in developing and validating models on different spatial and temporal scales.
Quynh T. Nguyen, Marianne Glasius, Lise L. Sørensen, Bjarne Jensen, Henrik Skov, Wolfram Birmili, Alfred Wiedensohler, Adam Kristensson, Jacob K. Nøjgaard, and Andreas Massling
Atmos. Chem. Phys., 16, 11319–11336, https://doi.org/10.5194/acp-16-11319-2016, https://doi.org/10.5194/acp-16-11319-2016, 2016
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Aerosol particles strongly influence climate change as they can absorb or reflect solar radiation. This work investigates aerosol particles in the remote northern Arctic. "Newly born" particles are small, then they "age" and grow in size due to different mechanisms. The results showed that during the polar night and especially Arctic spring, particles were likely transported from longer distances and were aged. During summer, "younger" particles are observed, which might be linked to ozone.
Hélène Angot, Ashu Dastoor, Francesco De Simone, Katarina Gårdfeldt, Christian N. Gencarelli, Ian M. Hedgecock, Sarka Langer, Olivier Magand, Michelle N. Mastromonaco, Claus Nordstrøm, Katrine A. Pfaffhuber, Nicola Pirrone, Andrei Ryjkov, Noelle E. Selin, Henrik Skov, Shaojie Song, Francesca Sprovieri, Alexandra Steffen, Kenjiro Toyota, Oleg Travnikov, Xin Yang, and Aurélien Dommergue
Atmos. Chem. Phys., 16, 10735–10763, https://doi.org/10.5194/acp-16-10735-2016, https://doi.org/10.5194/acp-16-10735-2016, 2016
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This is a synthesis of the atmospheric mercury (Hg) monitoring data available in recent years (2011–2015) in the Arctic and in Antarctica along with a comparison of these observations with numerical simulations using four cutting-edge global models. Based on this comparison, we discuss whether the processes that affect atmospheric Hg seasonality and interannual variability are appropriately represented in the models, and identify remaining research gaps.
N. Evangeliou, Y. Balkanski, W. M. Hao, A. Petkov, R. P. Silverstein, R. Corley, B. L. Nordgren, S. P. Urbanski, S. Eckhardt, A. Stohl, P. Tunved, S. Crepinsek, A. Jefferson, S. Sharma, J. K. Nøjgaard, and H. Skov
Atmos. Chem. Phys., 16, 7587–7604, https://doi.org/10.5194/acp-16-7587-2016, https://doi.org/10.5194/acp-16-7587-2016, 2016
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In this study, we focused on how vegetation fires that occurred in northern Eurasia during the period 2002–2013 influenced the budget of BC in the Arctic. An average area of 250 000 km2 yr−1 was burned in northern Eurasia and the global emissions of BC ranged between 8.0 and 9.5 Tg yr−1, while 102 ± 29 kt yr−1 BC from biomass burning was deposited on the Arctic. About 46 % of the Arctic BC from vegetation fires originated from Siberia, 6 % from Kazakhstan, 5 % from Europe, and about 1 % from Mon
T.-B. Ottosen, K. E. Kakosimos, C. Johansson, O. Hertel, J. Brandt, H. Skov, R. Berkowicz, T. Ellermann, S. S. Jensen, and M. Ketzel
Geosci. Model Dev., 8, 3231–3245, https://doi.org/10.5194/gmd-8-3231-2015, https://doi.org/10.5194/gmd-8-3231-2015, 2015
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Semi-parameterised street canyon models are popular due to their speed and low input requirements. One often-used assumption is that emissions are homogeneously distributed in the entire length and width of the street. It is thus the aim of the present study to analyse the impact of this assumption by implementing an inhomogeneous emission geometry scheme and validating it. The results show an improved performance, however, confounded by challenges in estimating the emissions accurately.
A. Massling, I. E. Nielsen, D. Kristensen, J. H. Christensen, L. L. Sørensen, B. Jensen, Q. T. Nguyen, J. K. Nøjgaard, M. Glasius, and H. Skov
Atmos. Chem. Phys., 15, 9681–9692, https://doi.org/10.5194/acp-15-9681-2015, https://doi.org/10.5194/acp-15-9681-2015, 2015
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Aerosols particles reach via long-range transport the high Arctic and have significant impacts on Arctic climate. This article demonstrates the comparison of measured and modeled aerosol mass concentrations for black carbon and sulfate particles at a high Arctic site. Based on the findings aging processes during transport seem to prolong the lifetimes of the two species and favor the possibility for their transport to the high Arctic.
S. Eckhardt, B. Quennehen, D. J. L. Olivié, T. K. Berntsen, R. Cherian, J. H. Christensen, W. Collins, S. Crepinsek, N. Daskalakis, M. Flanner, A. Herber, C. Heyes, Ø. Hodnebrog, L. Huang, M. Kanakidou, Z. Klimont, J. Langner, K. S. Law, M. T. Lund, R. Mahmood, A. Massling, S. Myriokefalitakis, I. E. Nielsen, J. K. Nøjgaard, J. Quaas, P. K. Quinn, J.-C. Raut, S. T. Rumbold, M. Schulz, S. Sharma, R. B. Skeie, H. Skov, T. Uttal, K. von Salzen, and A. Stohl
Atmos. Chem. Phys., 15, 9413–9433, https://doi.org/10.5194/acp-15-9413-2015, https://doi.org/10.5194/acp-15-9413-2015, 2015
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The concentrations of sulfate, black carbon and other aerosols in the Arctic are characterized by high values in late winter and spring (so-called Arctic Haze) and low values in summer. Models have long been struggling to capture this seasonality. In this study, we evaluate sulfate and BC concentrations from different updated models and emissions against a comprehensive pan-Arctic measurement data set. We find that the models improved but still struggle to get the maximum concentrations.
N. Kivekäs, A. Massling, H. Grythe, R. Lange, V. Rusnak, S. Carreno, H. Skov, E. Swietlicki, Q. T. Nguyen, M. Glasius, and A. Kristensson
Atmos. Chem. Phys., 14, 8255–8267, https://doi.org/10.5194/acp-14-8255-2014, https://doi.org/10.5194/acp-14-8255-2014, 2014
A. M. K. Hansen, K. Kristensen, Q. T. Nguyen, A. Zare, F. Cozzi, J. K. Nøjgaard, H. Skov, J. Brandt, J. H. Christensen, J. Ström, P. Tunved, R. Krejci, and M. Glasius
Atmos. Chem. Phys., 14, 7807–7823, https://doi.org/10.5194/acp-14-7807-2014, https://doi.org/10.5194/acp-14-7807-2014, 2014
Related subject area
Subject: Gases | Research Activity: Field Measurements | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Volatile organic compound sources and impacts in an urban Mediterranean area (Marseille, France)
Short-lived organic nitrates in a suburban temperate forest: an indication of efficient assimilation of reactive nitrogen by the biosphere?
Spatiotemporal variations in atmospheric CH4 concentrations and enhancements in northern China based on a comprehensive dataset: ground-based observations, TROPOMI data, inventory data, and inversions
Marine emissions and trade winds control the atmospheric nitrous oxide in the Galapagos Islands
Measurement report: A complex street-level air quality observation campaign in a heavy-traffic area utilizing the multivariate adaptive regression splines method for field calibration of low-cost sensors
The impact of organic nitrates on summer ozone formation in Shanghai, China
Differences in the key volatile organic compound species between their emitted and ambient concentrations in ozone formation
Mechanistic insights into chloroacetic acid production from atmospheric multiphase volatile organic compound–chlorine chemistry
Understanding summertime H2O2 chemistry in North China Plain through observations and modelling studies
Accurate elucidation of oxidation under heavy ozone pollution: a full suite of radical measurements in the chemically complex atmosphere
Carbonyl compounds from typical combustion sources: emission characteristics, influencing factors, and their contribution to ozone formation
Emissions of intermediate-volatility and semi-volatile organic compounds (I/SVOCs) from different cumulative-mileage diesel vehicles at various ambient temperatures
Characterization of nitrous acid and its potential effects on secondary pollution in the warm season in Beijing urban areas
Vertical changes in volatile organic compounds (VOCs) and impacts on photochemical ozone formation
Diurnal, seasonal, and interannual variations in δ(18O) of atmospheric O2 and its application to evaluate natural and anthropogenic changes in oxygen, carbon, and water cycles
Cloud processing of dimethyl sulfide (DMS) oxidation products limits sulfur dioxide (SO2) and carbonyl sulfide (OCS) production in the eastern North Atlantic marine boundary layer
Atmospheric carbonyl compounds are crucial in regional ozone heavy pollution: insights from the Chengdu Plain Urban Agglomeration, China
Ozone (O3) observations in Saxony, Germany for 1997–2020: Trends, modelling and implications for O3 control
Understanding summertime peroxyacetyl nitrate (PAN) formation and its relation to aerosol pollution: insights from high-resolution measurements and modeling
Measurement report: Exploring the variations in ambient BTEX in urban Europe and their environmental health implications
Seasonal air concentration variability, gas–particle partitioning, precipitation scavenging, and air–water equilibrium of organophosphate esters in southern Canada
Global Ground-based Tropospheric Ozone Measurements: Reference Data and Individual Site Trends (2000–2022) from the TOAR-II/HEGIFTOM Project
Tracing elevated abundance of CH2Cl2 in the subarctic upper troposphere to the Asian Summer Monsoon
Measurement report: Surface exchange fluxes of HONO during the growth process of paddy fields in the Huaihe River Basin, China
Hemispheric differences in ozone across the stratosphere-troposphere exchange region
Molecular and seasonal characteristics of organic vapors in urban Beijing: insights from Vocus-PTR measurements
The variations in volatile organic compounds based on the policy change for Omicron in the traffic hub of Zhengzhou
On the dynamics of ozone depletion events at Villum Research Station in the High Arctic
Measurement report: Long-term measurements of surface ozone and trends in semi-natural sub-Saharan African ecosystems
Characterization of biogenic volatile organic compounds and their oxidation products in a stressed spruce-dominated forest close to a biogas power plant
Reactive chlorine-, sulfur-, and nitrogen-containing volatile organic compounds impact atmospheric chemistry in the megacity of Delhi during both clean and extremely polluted seasons
Analysis of the day-to-day variability of ozone vertical profiles in the lower troposphere during the 2022 Paris ACROSS campaign
Significant influence of oxygenated volatile organic compounds on atmospheric chemistry analysis: A case study in a typical industrial city in China
Ozone deposition measurements over wheat fields in the North China Plain: variability and related factors of deposition flux and velocity
Consistency evaluation of tropospheric ozone from ozonesonde and IAGOS (In-service Aircraft for a Global Observing System) observations: vertical distribution, ozonesonde types, and station–airport distance
CO2 and CO temporal variability over Mexico City from ground-based total column and surface measurements
Investigating carbonyl compounds above the Amazon rainforest using a proton-transfer-reaction time-of-flight mass spectrometer (PTR-ToF-MS) with NO+ chemical ionization
Measurement report: In-flight and ground-based measurements of nitrogen oxide emissions from latest-generation jet engines and 100 % sustainable aviation fuel
Observation and modelling of atmospheric OH and HO2 radicals at a subtropical rural site and implications for secondary pollutants
Measurement report: Sources, sinks, and lifetime of NOx in a suburban temperate forest at night
Measurement report: Urban ammonia and amines in Houston, Texas
Biomass-burning sources control ambient particulate matter, but traffic and industrial sources control volatile organic compound (VOC) emissions and secondary-pollutant formation during extreme pollution events in Delhi
Multi-year observations of variable incomplete combustion in the New York megacity
Observations of the vertical distributions of summertime atmospheric pollutants in Nam Co: OH production and source analysis
Measurement report: Elevated atmospheric ammonia may promote particle pH and HONO formation – insights from the COVID-19 pandemic
Measurement report: Vertical and temporal variability in the near-surface ozone production rate and sensitivity in an urban area in the Pearl River Delta region, China
Elevated oxidized mercury in the free troposphere: analytical advances and application at a remote continental mountaintop site
Using observed urban NOx sinks to constrain VOC reactivity and the ozone and radical budget in the Seoul Metropolitan Area
Real-world emission characteristics of VOCs from typical cargo ships and their potential contributions to secondary organic aerosol and O3 under low-sulfur fuel policies
NO3 reactivity during a summer period in a temperate forest below and above the canopy
Marvin Dufresne, Thérèse Salameh, Thierry Leonardis, Grégory Gille, Alexandre Armengaud, and Stéphane Sauvage
Atmos. Chem. Phys., 25, 5977–5999, https://doi.org/10.5194/acp-25-5977-2025, https://doi.org/10.5194/acp-25-5977-2025, 2025
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This paper discusses the 18-month-long measurement of non-methane hydrocarbons (NMHCs) in Marseille, where there was no measurement since early 2000, despite the impact of NMHCs on air quality and climate. Traffic-related sources are the largest contributor to NMHC concentrations in Marseille, and shipping strongly contributes to the formation of aerosols. Finally, the Covid-19 lockdown had an impact on NMHC concentrations, reaching a 50 % decrease for traffic-related sources.
Simone T. Andersen, Rolf Sander, Patrick Dewald, Laura Wüst, Tobias Seubert, Gunther N. T. E. Türk, Jan Schuladen, Max R. McGillen, Chaoyang Xue, Abdelwahid Mellouki, Alexandre Kukui, Vincent Michoud, Manuela Cirtog, Mathieu Cazaunau, Astrid Bauville, Hichem Bouzidi, Paola Formenti, Cyrielle Denjean, Jean-Claude Etienne, Olivier Garrouste, Christopher Cantrell, Jos Lelieveld, and John N. Crowley
Atmos. Chem. Phys., 25, 5893–5909, https://doi.org/10.5194/acp-25-5893-2025, https://doi.org/10.5194/acp-25-5893-2025, 2025
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Measurements and modelling of reactive nitrogen gases observed in a suburban temperate forest in Rambouillet, France, circa 50 km southwest of Paris in 2022 indicate that the biosphere rapidly scavenges organic nitrates of mixed biogenic and anthropogenic origin, resulting in short lifetimes for, for example, alkyl nitrates and peroxy nitrates.
Pengfei Han, Ning Zeng, Bo Yao, Wen Zhang, Weijun Quan, Pucai Wang, Ting Wang, Minqiang Zhou, Qixiang Cai, Yuzhong Zhang, Ruosi Liang, Wanqi Sun, and Shengxiang Liu
Atmos. Chem. Phys., 25, 4965–4988, https://doi.org/10.5194/acp-25-4965-2025, https://doi.org/10.5194/acp-25-4965-2025, 2025
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Methane (CH4) is a potent greenhouse gas. Northern China contributes a large proportion of CH4 emissions, yet large observation gaps exist. Here we compiled a comprehensive dataset, which is publicly available, that includes ground-based, satellite-based, inventory, and modeling results to show the CH4 concentrations, enhancements, and spatial–temporal variations. The data can benefit the research community and policy-makers for future observations, atmospheric inversions, and policy-making.
Timur Cinay, Dickon Young, Nazaret Narváez Jimenez, Cristina Vintimilla-Palacios, Ariel Pila Alonso, Paul B. Krummel, William Vizuete, and Andrew R. Babbin
Atmos. Chem. Phys., 25, 4703–4718, https://doi.org/10.5194/acp-25-4703-2025, https://doi.org/10.5194/acp-25-4703-2025, 2025
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We present the initial 15 months of nitrous oxide measurements from the Galapagos Emissions Monitoring Station. The observed variability in atmospheric mole fractions during this period can be linked to several factors: seasonal variations in trade wind speed and direction across the eastern Pacific, differences in the transport history of air masses sampled, and spatiotemporal heterogeneity in regional marine nitrous oxide emissions from the coastal upwelling systems of Peru and Chile.
Petra Bauerová, Josef Keder, Adriana Šindelářová, Ondřej Vlček, William Patiño, Pavel Krč, Jan Geletič, Hynek Řezníček, Martin Bureš, Kryštof Eben, Michal Belda, Jelena Radović, Vladimír Fuka, Radek Jareš, Igor Esau, and Jaroslav Resler
Atmos. Chem. Phys., 25, 4477–4504, https://doi.org/10.5194/acp-25-4477-2025, https://doi.org/10.5194/acp-25-4477-2025, 2025
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The study explored urban air quality in Prague using low-cost sensors and highlighted the multivariate adaptive regression splines (MARS) correction method's effectiveness in enhancing accuracy. Results showed traffic's impact on nitrogen dioxide levels and atmospheric dynamics on particulate matter. The research confirmed MARS-corrected sensors as cost-effective for monitoring, despite challenges like sensor ageing and data quality control.
Chunmeng Li, Xiaorui Chen, Haichao Wang, Tianyu Zhai, Xuefei Ma, Xinping Yang, Shiyi Chen, Min Zhou, Shengrong Lou, Xin Li, Limin Zeng, and Keding Lu
Atmos. Chem. Phys., 25, 3905–3918, https://doi.org/10.5194/acp-25-3905-2025, https://doi.org/10.5194/acp-25-3905-2025, 2025
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This study reports an observation of organic nitrate (including total peroxy nitrates and total alkyl nitrates) in Shanghai, China, during the summer of 2021, by homemade thermal dissociation cavity-enhanced absorption spectroscopy (TD-CEAS; Atmos. Meas. Tech., 14, 4033–4051, 2021). The distribution of organic nitrates and their effects on local ozone production are analyzed based on field observations in conjunction with model simulations.
Xudong Zheng and Shaodong Xie
Atmos. Chem. Phys., 25, 3807–3820, https://doi.org/10.5194/acp-25-3807-2025, https://doi.org/10.5194/acp-25-3807-2025, 2025
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To reduce uncertainties in identifying the key volatile organic compounds (VOCs) in ozone (O3) formation from ambient concentrations, this study comprehensively calculates the emitted VOC concentrations during both nighttime and daytime using the nitrate radical, O3, and hydroxyl radical reaction rates and ambient VOC concentrations. Based on the emitted concentrations, isoprene is one of the top three species contributing to O3 formation, which may be overlooked in observed concentrations.
Mingxue Li, Men Xia, Chunshui Lin, Yifan Jiang, Weihang Sun, Yurun Wang, Yingnan Zhang, Maoxia He, and Tao Wang
Atmos. Chem. Phys., 25, 3753–3764, https://doi.org/10.5194/acp-25-3753-2025, https://doi.org/10.5194/acp-25-3753-2025, 2025
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Our field campaigns observed a strong diel pattern of chloroacetic acid as well as a strong correlation between its level and that of reactive chlorine species at a coastal site. Using quantum chemical calculations and box model simulation with an updated Master Chemical Mechanism, we found that the formation pathway of chloroacetic acid involved multiphase processes. Our study enhances understanding of atmospheric organic chlorine chemistry and emphasizes the importance of multiphase reactions.
Can Ye, Pengfei Liu, Chaoyang Xue, Chenglong Zhang, Zhuobiao Ma, Chengtang Liu, Junfeng Liu, Keding Lu, Yujing Mu, and Yuanhang Zhang
EGUsphere, https://doi.org/10.5194/egusphere-2025-795, https://doi.org/10.5194/egusphere-2025-795, 2025
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This study investigates H2O2 chemistry in rural North China. The observed H2O2 showed distinct diurnal variations influenced by photochemical reactions. A box model revealed that H2O2 is primarily produced by HO2 recombination and removed mainly via particle uptake. Reductions in NOx, PM2.5, and alkanes raised H2O2 levels, while cutting alkenes, aromatics, CO, and HONO lowered them. A dual strategy focusing on VOCs and NOx control is essential to reduce both H2O2 and ozone pollution.
Renzhi Hu, Guoxian Zhang, Haotian Cai, Jingyi Guo, Keding Lu, Xin Li, Shengrong Lou, Zhaofeng Tan, Changjin Hu, Pinhua Xie, and Wenqing Liu
Atmos. Chem. Phys., 25, 3011–3028, https://doi.org/10.5194/acp-25-3011-2025, https://doi.org/10.5194/acp-25-3011-2025, 2025
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A full suite of radical measurements (OH, HO2, RO2, and kOH) was established to accurately elucidate the limitations of oxidation in a chemically complex atmosphere. Sensitivity tests revealed that the incorporation of complex processes enabled a balance in both radical concentrations and coordinate ratios, effectively addressing the deficiency in the ozone generation mechanism. The full-chain radical detection bridged the gap between the photochemistry and the intensive oxidation level.
Yanjie Lu, Xinxin Feng, Yanli Feng, Minjun Jiang, Yu Peng, Tian Chen, and Yingjun Chen
EGUsphere, https://doi.org/10.5194/egusphere-2025-131, https://doi.org/10.5194/egusphere-2025-131, 2025
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The EFs of CCs from biomass burning (BB) is an order of magnitude higher than that from on-road sources. Fuel type determines the emission characteristics and composition of CCs. The formation of CCs from solid and liquid fuel sources is respectively controlled by combustion temperature and emission standards. In addition, biomass burning and agricultural machinery sources significantly contribute to the oxidizing capacity of regional atmospheres.
Shuwen Guo, Xuan Zheng, Xiao He, Lewei Zeng, Liqiang He, Xian Wu, Yifei Dai, Zihao Huang, Ting Chen, Shupei Xiao, Yan You, Sheng Xiang, Shaojun Zhang, Jingkun Jiang, and Ye Wu
Atmos. Chem. Phys., 25, 2695–2705, https://doi.org/10.5194/acp-25-2695-2025, https://doi.org/10.5194/acp-25-2695-2025, 2025
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We considered two potential influencing factors of heavy-duty diesel vehicle emissions that are rarely mentioned in the literature: cumulative mileage and ambient temperatures. The results suggest that prolonged use of heavy-duty diesel vehicles and low ambient temperatures leads to reduced engine combustion efficiency, which in turn increases tailpipe emissions significantly.
Junling Li, Chaofan Lian, Mingyuan Liu, Hao Zhang, Yongxin Yan, Yufei Song, Chun Chen, Jiaqi Wang, Haijie Zhang, Yanqin Ren, Yucong Guo, Weigang Wang, Yisheng Xu, Hong Li, Jian Gao, and Maofa Ge
Atmos. Chem. Phys., 25, 2551–2568, https://doi.org/10.5194/acp-25-2551-2025, https://doi.org/10.5194/acp-25-2551-2025, 2025
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As a key source of hydroxyl (OH) radical, nitrous acid (HONO) has attracted much attention for its important role in the atmospheric oxidant capacity (AOC) increase. In this study, we made a comparison of the ambient levels, variation patterns, sources, and formation pathway in the warm season on the basis of continuous intensive observations at an urban site of Beijing. This work highlights the importance of HONO for the AOC in the warm season.
Xiao-Bing Li, Bin Yuan, Yibo Huangfu, Suxia Yang, Xin Song, Jipeng Qi, Xianjun He, Sihang Wang, Yubin Chen, Qing Yang, Yongxin Song, Yuwen Peng, Guiqian Tang, Jian Gao, Dasa Gu, and Min Shao
Atmos. Chem. Phys., 25, 2459–2472, https://doi.org/10.5194/acp-25-2459-2025, https://doi.org/10.5194/acp-25-2459-2025, 2025
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Online vertical gradient measurements of volatile organic compounds (VOCs), ozone, and NOx were conducted based on a 325 m tall tower in urban Beijing. Vertical changes in the concentrations, compositions, key drivers, and environmental impacts of VOCs were analyzed in this study. We find that VOC species display differentiated vertical variation patterns and distinct roles in contributing to photochemical ozone formation with increasing height in the urban planetary boundary layer.
Shigeyuki Ishidoya, Satoshi Sugawara, and Atsushi Okazaki
Atmos. Chem. Phys., 25, 1965–1987, https://doi.org/10.5194/acp-25-1965-2025, https://doi.org/10.5194/acp-25-1965-2025, 2025
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The 18O/16O ratio of atmospheric oxygen, δatm(18O), is higher than that of ocean water due to isotopic effects during biospheric activities. This is known as the Dole–Morita effect, and its millennial-scale variations are recorded in ice cores. However, small variations of δatm(18O) in the present day have never been detected so far. This paper presents the first observations of diurnal, seasonal, and secular variations in δatm(18O) and applies them to evaluate oxygen, carbon, and water cycles.
Delaney B. Kilgour, Christopher M. Jernigan, Olga Garmash, Sneha Aggarwal, Shengqian Zhou, Claudia Mohr, Matt E. Salter, Joel A. Thornton, Jian Wang, Paul Zieger, and Timothy H. Bertram
Atmos. Chem. Phys., 25, 1931–1947, https://doi.org/10.5194/acp-25-1931-2025, https://doi.org/10.5194/acp-25-1931-2025, 2025
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We report simultaneous measurements of dimethyl sulfide (DMS) and hydroperoxymethyl thioformate (HPMTF) in the eastern North Atlantic. We use an observationally constrained box model to show that cloud loss is the dominant sink of HPMTF in this region over 6 weeks, resulting in large reductions in DMS-derived products that contribute to aerosol formation and growth. Our findings indicate that fast cloud processing of HPMTF must be included in global models to accurately capture the sulfur cycle.
Jiemeng Bao, Xin Zhang, Zhenhai Wu, Li Zhou, Jun Qian, Qinwen Tan, Fumo Yang, Junhui Chen, Yunfeng Li, Hefan Liu, Liqun Deng, and Hong Li
Atmos. Chem. Phys., 25, 1899–1916, https://doi.org/10.5194/acp-25-1899-2025, https://doi.org/10.5194/acp-25-1899-2025, 2025
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We studied carbonyl compounds' role in ozone pollution in the Chengdu Plain Urban Agglomeration, China. During heavy pollution in August 2019, we measured carbonyls at nine sites and analyzed their impact. Areas with higher carbonyl levels, like Chengdu, had worse ozone pollution. While their abundance matters, chemical reactions with other pollutants are the main drivers. Our findings show regional cooperation is vital to reducing ozone pollution effectively.
Yaru Wang, Dominik van Pinxteren, Andreas Tilgner, Erik Hans Hoffmann, Max Hell, Susanne Bastian, and Hartmut Herrmann
EGUsphere, https://doi.org/10.5194/egusphere-2024-4202, https://doi.org/10.5194/egusphere-2024-4202, 2025
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Tropospheric ground-level ozone (O3) is a global air-quality pollutant and greenhouse gas. Long-term O3 trends from 16 stations in Saxony, Germany, were compared over three periods, revealing worsened O3 pollution over the last decade. O3 formation has been volatile organic compound (VOC)-limited at traffic and urban sites for the past 20 years. To mitigate O3 pollution, moderate nitrogen oxides and additional VOC controls, particularly in solvent use, should be prioritized in the coming years.
Baoye Hu, Naihua Chen, Rui Li, Mingqiang Huang, Jinsheng Chen, Youwei Hong, Lingling Xu, Xiaolong Fan, Mengren Li, Lei Tong, Qiuping Zheng, and Yuxiang Yang
Atmos. Chem. Phys., 25, 905–921, https://doi.org/10.5194/acp-25-905-2025, https://doi.org/10.5194/acp-25-905-2025, 2025
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Box modeling with the Master Chemical Mechanism (MCM) was used to explore summertime peroxyacetyl nitrate (PAN) formation and its link to aerosol pollution under high-ozone conditions. The MCM model is effective in the study of PAN photochemical formation and performed better during the clean period than the haze period. Machine learning analysis identified ammonia, nitrate, and fine particulate matter as the top three factors contributing to simulation bias.
Xiansheng Liu, Xun Zhang, Marvin Dufresne, Tao Wang, Lijie Wu, Rosa Lara, Roger Seco, Marta Monge, Ana Maria Yáñez-Serrano, Marie Gohy, Paul Petit, Audrey Chevalier, Marie-Pierre Vagnot, Yann Fortier, Alexia Baudic, Véronique Ghersi, Grégory Gille, Ludovic Lanzi, Valérie Gros, Leïla Simon, Heidi Héllen, Stefan Reimann, Zoé Le Bras, Michelle Jessy Müller, David Beddows, Siqi Hou, Zongbo Shi, Roy M. Harrison, William Bloss, James Dernie, Stéphane Sauvage, Philip K. Hopke, Xiaoli Duan, Taicheng An, Alastair C. Lewis, James R. Hopkins, Eleni Liakakou, Nikolaos Mihalopoulos, Xiaohu Zhang, Andrés Alastuey, Xavier Querol, and Thérèse Salameh
Atmos. Chem. Phys., 25, 625–638, https://doi.org/10.5194/acp-25-625-2025, https://doi.org/10.5194/acp-25-625-2025, 2025
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This study examines BTEX (benzene, toluene, ethylbenzene, xylenes) pollution in urban areas across seven European countries. Analyzing data from 22 monitoring sites, we found traffic and industrial activities significantly impact BTEX levels, with peaks during rush hours. The risk from BTEX exposure remains moderate, especially in high-traffic and industrial zones, highlighting the need for targeted air quality management to protect public health and improve urban air quality.
Yuening Li, Faqiang Zhan, Chubashini Shunthirasingham, Ying Duan Lei, Jenny Oh, Amina Ben Chaaben, Zhe Lu, Kelsey Lee, Frank A. P. C. Gobas, Hayley Hung, and Frank Wania
Atmos. Chem. Phys., 25, 459–472, https://doi.org/10.5194/acp-25-459-2025, https://doi.org/10.5194/acp-25-459-2025, 2025
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Organophosphate esters are important humanmade trace contaminants. Measuring them in the atmospheric gas phase, particles, precipitation, and surface water in Canada, we explore seasonal concentration variability, gas–particle partitioning, precipitation scavenging, and the air–water equilibrium. Whereas higher summer concentrations and efficient precipitation scavenging conform with expectations, the lack of a relationship between compound volatility and gas–particle partitioning is puzzling.
Roeland Van Malderen, Anne M. Thompson, Debra E. Kollonige, Ryan M. Stauffer, Herman G. J. Smit, Eliane Maillard Barras, Corinne Vigouroux, Irina Petropavlovskikh, Thierry Leblanc, Valérie Thouret, Pawel Wolff, Peter Effertz, David W. Tarasick, Deniz Poyraz, Gérard Ancellet, Marie-Renée De Backer, Stéphanie Evan, Victoria Flood, Matthias M. Frey, James W. Hannigan, José L. Hernandez, Marco Iarlori, Bryan J. Johnson, Nicholas Jones, Rigel Kivi, Emmanuel Mahieu, Glen McConville, Katrin Müller, Tomoo Nagahama, Justus Notholt, Ankie Piters, Natalia Prats, Richard Querel, Dan Smale, Wolfgang Steinbrecht, Kimberly Strong, and Ralf Sussmann
EGUsphere, https://doi.org/10.5194/egusphere-2024-3736, https://doi.org/10.5194/egusphere-2024-3736, 2025
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Tropospheric ozone is an important greenhouse gas and is an air pollutant. The time variability of tropospheric ozone is mainly driven by anthropogenic emissions. In this paper, we study the distribution and time variability of ozone from harmonized ground-based observations from five different measurement techniques. Our findings will provide clear standard references for atmospheric models and evolving tropospheric ozone satellite data for the 2000–2022 period.
Markus Jesswein, Valentin Lauther, Nicolas Emig, Peter Hoor, Timo Keber, Hans-Christoph Lachnitt, Linda Ort, Tanja Schuck, Johannes Strobel, Ronja Van Luijt, C. Michael Volk, Franziska Weyland, and Andreas Engel
EGUsphere, https://doi.org/10.5194/egusphere-2024-3946, https://doi.org/10.5194/egusphere-2024-3946, 2025
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The study investigates transport within the Asian Summer Monsoon, focussing on how CH2Cl2 reaches the subarctic tropopause region. Using data from the PHILEAS campaign in 2023, events with increased mixing ratios were detected. Their origin, the transport paths to the tropopause region and the potential entry into the stratosphere were analysed. The East Asian Summer Monsoon was identified as the main transport pathway, with only a small contribution to the stratosphere in the following days.
Fanhao Meng, Baobin Han, Min Qin, Wu Fang, Ke Tang, Dou Shao, Zhitang Liao, Jun Duan, Yan Feng, Yong Huang, Ting Ni, and Pinhua Xie
Atmos. Chem. Phys., 24, 14191–14208, https://doi.org/10.5194/acp-24-14191-2024, https://doi.org/10.5194/acp-24-14191-2024, 2024
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Comprehensive observations of HONO and NOx fluxes were conducted over paddy fields in the Huaihe River Basin. Consecutive peaks in HONO and NO fluxes suggest a potentially enhanced release of HONO and NO due to soil tillage, whereas waterlogged soil may inhibit microbial nitrification processes following irrigation. Notably, biological processes and light-driven NO2 reactions at the surface may serve as sources of HONO and influence the local HONO budget during rotary tillage.
Rodrigo J. Seguel, Charlie Opazo, Yann Cohen, Owen R. Cooper, Laura Gallardo, Björn-Martin Sinnhuber, Florian Obersteiner, Andreas Zahn, Peter Hoor, and Susanne Rohs
EGUsphere, https://doi.org/10.5194/egusphere-2024-3719, https://doi.org/10.5194/egusphere-2024-3719, 2024
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We explored differences in ozone levels between the Northern and Southern Hemispheres in the Stratosphere-troposphere exchange region. Using unique data from a research aircraft, we found significantly lower ozone levels (with stratospheric character) in the Southern Hemisphere, especially during years of severe ozone depletion. A Sudden Stratospheric Warming event in 2019 increased Southern Hemisphere ozone levels, highlighting the relationship between atmospheric events and ozone distribution.
Zhaojin An, Rujing Yin, Xinyan Zhao, Xiaoxiao Li, Yuyang Li, Yi Yuan, Junchen Guo, Yiqi Zhao, Xue Li, Dandan Li, Yaowei Li, Dongbin Wang, Chao Yan, Kebin He, Douglas R. Worsnop, Frank N. Keutsch, and Jingkun Jiang
Atmos. Chem. Phys., 24, 13793–13810, https://doi.org/10.5194/acp-24-13793-2024, https://doi.org/10.5194/acp-24-13793-2024, 2024
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Online Vocus-PTR measurements show the compositions and seasonal variations in organic vapors in urban Beijing. With enhanced sensitivity and mass resolution, various species at a level of sub-parts per trillion (ppt) and organics with multiple oxygens (≥ 3) were observed. The fast photooxidation process in summer leads to an increase in both concentration and proportion of organics with multiple oxygens, while, in other seasons, the variations in them could be influenced by mixed sources.
Bowen Zhang, Dong Zhang, Zhe Dong, Xinshuai Song, Ruiqin Zhang, and Xiao Li
Atmos. Chem. Phys., 24, 13587–13601, https://doi.org/10.5194/acp-24-13587-2024, https://doi.org/10.5194/acp-24-13587-2024, 2024
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To gain insight into the impact of changes due to epidemic control policies, we undertook continuous online monitoring of volatile organic compounds (VOCs) at an urban site in Zhengzhou over a 2-month period. This study examines the characteristics of VOCs, their sources, and their temporal evolution. It also assesses the impact of the policy change on VOC pollution during the monitoring period, thus providing a basis for further research on VOC pollution and source control.
Jakob Boyd Pernov, Jens Liengaard Hjorth, Lise Lotte Sørensen, and Henrik Skov
Atmos. Chem. Phys., 24, 13603–13631, https://doi.org/10.5194/acp-24-13603-2024, https://doi.org/10.5194/acp-24-13603-2024, 2024
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Arctic ozone depletion events (ODEs) occur every spring and have vast implications for the oxidizing capacity, radiative balance, and mercury oxidation. In this study, we analyze ozone, ODEs, and their connection to meteorological and air mass history variables through statistical analyses, back trajectories, and machine learning (ML) at Villum Research Station. ODEs are favorable under sunny, calm conditions with air masses arriving from northerly wind directions with sea ice contact.
Hagninou Elagnon Venance Donnou, Aristide Barthélémy Akpo, Money Ossohou, Claire Delon, Véronique Yoboué, Dungall Laouali, Marie Ouafo-Leumbe, Pieter Gideon Van Zyl, Ousmane Ndiaye, Eric Gardrat, Maria Dias-Alves, and Corinne Galy-Lacaux
Atmos. Chem. Phys., 24, 13151–13182, https://doi.org/10.5194/acp-24-13151-2024, https://doi.org/10.5194/acp-24-13151-2024, 2024
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Ozone is a secondary air pollutant that is detrimental to human and plant health. A better understanding of its chemical evolution is a challenge for Africa, where it is still undersampled. Out of 14 sites examined (1995–2020), high levels of O3 are reported in southern Africa. The dominant chemical processes leading to O3 formation are identified. A decrease in O3 is observed at Katibougou (Mali) and Banizoumbou (Niger), and an increase is found at Zoétélé (Cameroon) and Skukuza (South Africa).
Junwei Song, Georgios I. Gkatzelis, Ralf Tillmann, Nicolas Brüggemann, Thomas Leisner, and Harald Saathoff
Atmos. Chem. Phys., 24, 13199–13217, https://doi.org/10.5194/acp-24-13199-2024, https://doi.org/10.5194/acp-24-13199-2024, 2024
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Biogenic volatile organic compounds (BVOCs) and organic aerosol (OA) particles were measured online in a stressed spruce-dominated forest. OA was mainly attributed to the monoterpene oxidation products. The mixing ratios of BVOCs were higher than the values previously measured in other temperate forests. The results demonstrate that BVOCs are influenced not only by meteorology and biogenic emissions but also by local anthropogenic emissions and subsequent chemical transformation processes.
Sachin Mishra, Vinayak Sinha, Haseeb Hakkim, Arpit Awasthi, Sachin D. Ghude, Vijay Kumar Soni, Narendra Nigam, Baerbel Sinha, and Madhavan N. Rajeevan
Atmos. Chem. Phys., 24, 13129–13150, https://doi.org/10.5194/acp-24-13129-2024, https://doi.org/10.5194/acp-24-13129-2024, 2024
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We quantified 111 gases using mass spectrometry to understand how seasonal and emission changes lead from clean air in the monsoon season to extremely polluted air in the post-monsoon season in Delhi. Averaged total mass concentrations (260 µg m-3) were > 4 times in polluted periods, driven by biomass burning emissions and reduced atmospheric ventilation. Reactive gaseous nitrogen, chlorine, and sulfur compounds hitherto unreported from such a polluted environment were discovered.
Gérard Ancellet, Camille Viatte, Anne Boynard, François Ravetta, Jacques Pelon, Cristelle Cailteau-Fischbach, Pascal Genau, Julie Capo, Axel Roy, and Philippe Nédélec
Atmos. Chem. Phys., 24, 12963–12983, https://doi.org/10.5194/acp-24-12963-2024, https://doi.org/10.5194/acp-24-12963-2024, 2024
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Characterization of ozone pollution in urban areas benefited from a measurement campaign in summer 2022 in the Paris region. The analysis is based on 21 d of lidar and aircraft observations. The main objective is an analysis of the sensitivity of ozone pollution to the micrometeorological processes in the urban atmospheric boundary layer and the transport of regional pollution. The paper also discusses to what extent satellite observations can track observed ozone plumes.
Jingwen Dai, Kun Zhang, Yanli Feng, Xin Yi, Rui Li, Jin Xue, Qing Li, Lishu Shi, Jiaqiang Liao, Yanan Yi, Fangting Wang, Liumei Yang, Hui Chen, Ling Huang, Jiani Tan, Yangjun Wang, and Li Li
EGUsphere, https://doi.org/10.5194/egusphere-2024-3201, https://doi.org/10.5194/egusphere-2024-3201, 2024
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Oxygenated volatile organic compounds (OVOCs) are important ozone (O3) precursors. However, most of O3 formation analysis based on the box model (OBM) don't include OVOCs constraint To access the interference of OVOCs on O3 simulation, this study conducted field campaign and OBM analysis. The results indicates that no OVOCs constraint in the OBM can lead to overestimate of OVOCs, free radicals, and O3.
Xiaoyi Zhang, Wanyun Xu, Weili Lin, Gen Zhang, Jinjian Geng, Li Zhou, Huarong Zhao, Sanxue Ren, Guangsheng Zhou, Jianmin Chen, and Xiaobin Xu
Atmos. Chem. Phys., 24, 12323–12340, https://doi.org/10.5194/acp-24-12323-2024, https://doi.org/10.5194/acp-24-12323-2024, 2024
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Ozone (O3) deposition is a key process that removes surface O3, affecting air quality, ecosystems and climate change. We conducted O3 deposition measurement over a wheat canopy using a newly relaxed eddy accumulation flux system. Large variabilities in O3 deposition were detected, mainly determined by crop growth and modulated by various environmental factors. More O3 deposition observations over different surfaces are needed for exploring deposition mechanisms and model optimization.
Honglei Wang, David W. Tarasick, Jane Liu, Herman G. J. Smit, Roeland Van Malderen, Lijuan Shen, Romain Blot, and Tianliang Zhao
Atmos. Chem. Phys., 24, 11927–11942, https://doi.org/10.5194/acp-24-11927-2024, https://doi.org/10.5194/acp-24-11927-2024, 2024
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In this study, we identify 23 suitable pairs of sites from World Ozone and Ultraviolet Radiation Data Centre (WOUDC) and In-service Aircraft for a Global Observing System (IAGOS) datasets (1995 to 2021), compare the average vertical distributions of tropospheric O3 from ozonesonde and aircraft measurements, and analyze the differences based on ozonesonde type and station–airport distance.
Noémie Taquet, Wolfgang Stremme, María Eugenia González del Castillo, Victor Almanza, Alejandro Bezanilla, Olivier Laurent, Carlos Alberti, Frank Hase, Michel Ramonet, Thomas Lauvaux, Ke Che, and Michel Grutter
Atmos. Chem. Phys., 24, 11823–11848, https://doi.org/10.5194/acp-24-11823-2024, https://doi.org/10.5194/acp-24-11823-2024, 2024
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We characterize the variability in CO and CO2 emissions over Mexico City from long-term time-resolved Fourier transform infrared spectroscopy solar absorption and surface measurements from 2013 to 2021. Using the average intraday CO growth rate from total columns, the average CO / CO2 ratio and TROPOMI data, we estimate the interannual variability in the CO and CO2 anthropogenic emissions of Mexico City, highlighting the effect of an unprecedented drop in activity due to the COVID-19 lockdown.
Akima Ringsdorf, Achim Edtbauer, Bruna Holanda, Christopher Poehlker, Marta O. Sá, Alessandro Araújo, Jürgen Kesselmeier, Jos Lelieveld, and Jonathan Williams
Atmos. Chem. Phys., 24, 11883–11910, https://doi.org/10.5194/acp-24-11883-2024, https://doi.org/10.5194/acp-24-11883-2024, 2024
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We show the average height distribution of separately observed aldehydes and ketones over a day and discuss their rainforest-specific sources and sinks as well as their seasonal changes above the Amazon. Ketones have much longer atmospheric lifetimes than aldehydes and thus different implications for atmospheric chemistry. However, they are commonly observed together, which we overcome by measuring with a NO+ chemical ionization mass spectrometer for the first time in the Amazon rainforest.
Theresa Harlass, Rebecca Dischl, Stefan Kaufmann, Raphael Märkl, Daniel Sauer, Monika Scheibe, Paul Stock, Tiziana Bräuer, Andreas Dörnbrack, Anke Roiger, Hans Schlager, Ulrich Schumann, Magdalena Pühl, Tobias Schripp, Tobias Grein, Linda Bondorf, Charles Renard, Maxime Gauthier, Mark Johnson, Darren Luff, Paul Madden, Peter Swann, Denise Ahrens, Reetu Sallinen, and Christiane Voigt
Atmos. Chem. Phys., 24, 11807–11822, https://doi.org/10.5194/acp-24-11807-2024, https://doi.org/10.5194/acp-24-11807-2024, 2024
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Emissions from aircraft have a direct impact on our climate. Here, we present airborne and ground-based measurement data of nitrogen oxides that were collected in the exhaust of an Airbus aircraft. We study the impact of burning fossil and sustainable aviation fuel on nitrogen oxide emissions at different engine settings related to combustor temperature, pressure and fuel flow. Further, we compare observations with engine emission models.
Zhouxing Zou, Tianshu Chen, Qianjie Chen, Weihang Sun, Shichun Han, Zhuoyue Ren, Xinyi Li, Wei Song, Aoqi Ge, Qi Wang, Xiao Tian, Chenglei Pei, Xinming Wang, Yanli Zhang, and Tao Wang
EGUsphere, https://doi.org/10.5194/egusphere-2024-3210, https://doi.org/10.5194/egusphere-2024-3210, 2024
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We measured ambient OH and HO2 concentrations at a subtropical rural site and compared our observations with model results. During warm periods, the model overestimated the concentrations of OH and HO2, leading to overestimation of ozone and nitric acid production. Our findings highlight the need to better understand how OH and HO2are formed and removed, which is important for accurate air quality and climate predictions.
Simone T. Andersen, Max R. McGillen, Chaoyang Xue, Tobias Seubert, Patrick Dewald, Gunther N. T. E. Türk, Jan Schuladen, Cyrielle Denjean, Jean-Claude Etienne, Olivier Garrouste, Marina Jamar, Sergio Harb, Manuela Cirtog, Vincent Michoud, Mathieu Cazaunau, Antonin Bergé, Christopher Cantrell, Sebastien Dusanter, Bénédicte Picquet-Varrault, Alexandre Kukui, Abdelwahid Mellouki, Lucy J. Carpenter, Jos Lelieveld, and John N. Crowley
Atmos. Chem. Phys., 24, 11603–11618, https://doi.org/10.5194/acp-24-11603-2024, https://doi.org/10.5194/acp-24-11603-2024, 2024
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Using measurements of various trace gases in a suburban forest near Paris in the summer of 2022, we were able to gain insight into the sources and sinks of NOx (NO+NO2) with a special focus on their nighttime chemical and physical loss processes. NO was observed as a result of nighttime soil emissions when O3 levels were strongly depleted by deposition. NO oxidation products were not observed at night, indicating that soil and/or foliar surfaces are an efficient sink of reactive N.
Lee Tiszenkel, James H. Flynn, and Shan-Hu Lee
Atmos. Chem. Phys., 24, 11351–11363, https://doi.org/10.5194/acp-24-11351-2024, https://doi.org/10.5194/acp-24-11351-2024, 2024
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Ammonia and amines are important ingredients for aerosol formation in urban environments, but the measurements of these compounds are extremely challenging. Our observations show that urban ammonia and amines in Houston are emitted from urban sources, and diurnal variations in their concentrations are likely governed by gas-to-particle conversion and emissions.
Arpit Awasthi, Baerbel Sinha, Haseeb Hakkim, Sachin Mishra, Varkrishna Mummidivarapu, Gurmanjot Singh, Sachin D. Ghude, Vijay Kumar Soni, Narendra Nigam, Vinayak Sinha, and Madhavan N. Rajeevan
Atmos. Chem. Phys., 24, 10279–10304, https://doi.org/10.5194/acp-24-10279-2024, https://doi.org/10.5194/acp-24-10279-2024, 2024
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We use 111 volatile organic compounds (VOCs), PM10, and PM2.5 in a positive matrix factorization (PMF) model to resolve 11 pollution sources validated with chemical fingerprints. Crop residue burning and heating account for ~ 50 % of the PM, while traffic and industrial emissions dominate the gas-phase VOC burden and formation potential of secondary organic aerosols (> 60 %). Non-tailpipe emissions from compressed-natural-gas-fuelled commercial vehicles dominate the transport sector's PM burden.
Luke D. Schiferl, Cong Cao, Bronte Dalton, Andrew Hallward-Driemeier, Ricardo Toledo-Crow, and Róisín Commane
Atmos. Chem. Phys., 24, 10129–10142, https://doi.org/10.5194/acp-24-10129-2024, https://doi.org/10.5194/acp-24-10129-2024, 2024
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Carbon monoxide (CO) is an air pollutant and an important indicator of the incomplete combustion of fossil fuels in cities. Using 4 years of winter and spring observations in New York City, we found that both the magnitude and variability of CO from the metropolitan area are greater than expected. Transportation emissions cannot explain the missing and variable CO, which points to energy from buildings as a likely underappreciated source of urban air pollution and greenhouse gas emissions.
Chengzhi Xing, Cheng Liu, Chunxiang Ye, Jingkai Xue, Hongyu Wu, Xiangguang Ji, Jinping Ou, and Qihou Hu
Atmos. Chem. Phys., 24, 10093–10112, https://doi.org/10.5194/acp-24-10093-2024, https://doi.org/10.5194/acp-24-10093-2024, 2024
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We identified the contributions of ozone (O3) and nitrous acid (HONO) to the production rates of hydroxide (OH) in vertical space on the Tibetan Plateau (TP). A new insight was offered: the contributions of HONO and O3 to the production rates of OH on the TP are even greater than in lower-altitudes areas. This study enriches the understanding of vertical distribution of atmospheric components and explains the strong atmospheric oxidation capacity (AOC) on the TP.
Xinyuan Zhang, Lingling Wang, Nan Wang, Shuangliang Ma, Shenbo Wang, Ruiqin Zhang, Dong Zhang, Mingkai Wang, and Hongyu Zhang
Atmos. Chem. Phys., 24, 9885–9898, https://doi.org/10.5194/acp-24-9885-2024, https://doi.org/10.5194/acp-24-9885-2024, 2024
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This study highlights the importance of the redox reaction of NO2 with SO2 based on actual atmospheric observations. The particle pH in future China is expected to rise steadily. Consequently, this reaction could become a significant source of HONO in China. Therefore, it is crucial to coordinate the control of SO2, NOx, and NH3 emissions to avoid a rapid increase in the particle pH.
Jun Zhou, Chunsheng Zhang, Aiming Liu, Bin Yuan, Yan Wang, Wenjie Wang, Jie-Ping Zhou, Yixin Hao, Xiao-Bing Li, Xianjun He, Xin Song, Yubin Chen, Suxia Yang, Shuchun Yang, Yanfeng Wu, Bin Jiang, Shan Huang, Junwen Liu, Yuwen Peng, Jipeng Qi, Minhui Deng, Bowen Zhong, Yibo Huangfu, and Min Shao
Atmos. Chem. Phys., 24, 9805–9826, https://doi.org/10.5194/acp-24-9805-2024, https://doi.org/10.5194/acp-24-9805-2024, 2024
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In-depth understanding of the near-ground vertical variability in photochemical ozone (O3) formation is crucial for mitigating O3 pollution. Utilizing a self-built vertical observation system, a direct net photochemical O3 production rate detection system, and an observation-based model, we diagnosed the vertical distributions and formation mechanism of net photochemical O3 production rates and sensitivity in the Pearl River Delta region, one of the most O3-polluted areas in China.
Eleanor J. Derry, Tyler R. Elgiar, Taylor Y. Wilmot, Nicholas W. Hoch, Noah S. Hirshorn, Peter Weiss-Penzias, Christopher F. Lee, John C. Lin, A. Gannet Hallar, Rainer Volkamer, Seth N. Lyman, and Lynne E. Gratz
Atmos. Chem. Phys., 24, 9615–9643, https://doi.org/10.5194/acp-24-9615-2024, https://doi.org/10.5194/acp-24-9615-2024, 2024
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Mercury (Hg) is a globally distributed neurotoxic pollutant. Atmospheric deposition is the main source of Hg in ecosystems. However, measurement biases hinder understanding of the origins and abundance of the more bioavailable oxidized form. We used an improved, calibrated measurement system to study air mass composition and transport of atmospheric Hg at a remote mountaintop site in the central US. Oxidized Hg originated upwind in the low to middle free troposphere under clean, dry conditions.
Benjamin A. Nault, Katherine R. Travis, James H. Crawford, Donald R. Blake, Pedro Campuzano-Jost, Ronald C. Cohen, Joshua P. DiGangi, Glenn S. Diskin, Samuel R. Hall, L. Gregory Huey, Jose L. Jimenez, Kyung-Eun Min, Young Ro Lee, Isobel J. Simpson, Kirk Ullmann, and Armin Wisthaler
Atmos. Chem. Phys., 24, 9573–9595, https://doi.org/10.5194/acp-24-9573-2024, https://doi.org/10.5194/acp-24-9573-2024, 2024
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Ozone (O3) is a pollutant formed from the reactions of gases emitted from various sources. In urban areas, the density of human activities can increase the O3 formation rate (P(O3)), thus impacting air quality and health. Observations collected over Seoul, South Korea, are used to constrain P(O3). A high local P(O3) was found; however, local P(O3) was partly reduced due to compounds typically ignored. These observations also provide constraints for unmeasured compounds that will impact P(O3).
Fan Zhang, Binyu Xiao, Zeyu Liu, Yan Zhang, Chongguo Tian, Rui Li, Can Wu, Yali Lei, Si Zhang, Xinyi Wan, Yubao Chen, Yong Han, Min Cui, Cheng Huang, Hongli Wang, Yingjun Chen, and Gehui Wang
Atmos. Chem. Phys., 24, 8999–9017, https://doi.org/10.5194/acp-24-8999-2024, https://doi.org/10.5194/acp-24-8999-2024, 2024
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Mandatory use of low-sulfur fuel due to global sulfur limit regulations means large uncertainties in volatile organic compound (VOC) emissions. On-board tests of VOCs from nine cargo ships in China were carried out. Results showed that switching from heavy-fuel oil to diesel increased emission factor VOCs by 48 % on average, enhancing O3 and the secondary organic aerosol formation potential. Thus, implementing a global ultra-low-sulfur oil policy needs to be optimized in the near future.
Patrick Dewald, Tobias Seubert, Simone T. Andersen, Gunther N. T. E. Türk, Jan Schuladen, Max R. McGillen, Cyrielle Denjean, Jean-Claude Etienne, Olivier Garrouste, Marina Jamar, Sergio Harb, Manuela Cirtog, Vincent Michoud, Mathieu Cazaunau, Antonin Bergé, Christopher Cantrell, Sebastien Dusanter, Bénédicte Picquet-Varrault, Alexandre Kukui, Chaoyang Xue, Abdelwahid Mellouki, Jos Lelieveld, and John N. Crowley
Atmos. Chem. Phys., 24, 8983–8997, https://doi.org/10.5194/acp-24-8983-2024, https://doi.org/10.5194/acp-24-8983-2024, 2024
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In the scope of a field campaign in a suburban forest near Paris in the summer of 2022, we measured the reactivity of the nitrate radical NO3 towards biogenic volatile organic compounds (BVOCs; e.g. monoterpenes) mainly below but also above the canopy. NO3 reactivity was the highest during nights with strong temperature inversions and decreased strongly with height. Reactions with BVOCs were the main removal process of NO3 throughout the diel cycle below the canopy.
Cited articles
AMAP: AMAP Assessment 2011: Mercury in the Arctic, Arctic Monitoring and
Assessment Programme (AMAP), Oslo, Norway, xiv + 193 pp., 2011.
Ambrose, J. L.: Improved methods for signal processing in measurements of
mercury by Tekran® 2537A and 2537B instruments, Atmos. Meas. Tech., 10, 5063–5073, https://doi.org/10.5194/amt-10-5063-2017, 2017.
Andreae, M. O.: Emission of trace gases and aerosols from biomass burning – an updated assessment, Atmos. Chem. Phys., 19, 8523–8546,
https://doi.org/10.5194/acp-19-8523-2019, 2019.
Angot, H., Dastoor, A., De Simone, F., Gårdfeldt, K., Gencarelli, C. N.,
Hedgecock, I. M., Langer, S., Magand, O., Mastromonaco, M. N., Nordstrøm,
C., Pfaffhuber, K. A., Pirrone, N., Ryjkov, A., Selin, N. E., Skov, H., Song, S., Sprovieri, F., Steffen, A., Toyota, K., Travnikov, O., Yang, X., and Dommergue, A.: Chemical cycling and deposition of atmospheric mercury in
polar regions: review of recent measurements and comparison with models,
Atmos. Chem. Phys., 16, 10735–10763, https://doi.org/10.5194/acp-16-10735-2016, 2016.
Ariya, P. A., Dastroor, A. P., Amyot, M., Schroeder, W. H., Barrie, L., Anlauf, K., Raofie, F., Ryzhkov, A., Davignon, D., Lalonde, J., and Steffen,
A.: The Arctic: a sink for mercury, Tellus B, 56, 397–403, https://doi.org/10.3402/tellusb.v56i5.16458, 2004.
Ariya, P. A., Amyot, M., Dastoor, A., Deeds, D., Feinberg, A., Kos, G., Poulain, A., Ryjkov, A., Semeniuk, K., Subir, M., and Toyota, K.: Mercury
physicochemical and biogeochemical transformation in the atmosphere and at
atmospheric interfaces: a review and future directions, Chem. Rev., 115, 3760–3802, https://doi.org/10.1021/cr500667e, 2015.
Arnold, S. R., Emmons, L. K., Monks, S. A., Law, K. S., Ridley, D. A., Turquety, S., Tilmes, S., Thomas, J. L., Bouarar, I., Flemming, J., Huijnen,
V., Mao, J., Duncan, B. N., Steenrod, S., Yoshida, Y., Langner, J., and
Long, Y.: Biomass burning influence on high-latitude tropospheric ozone and
reactive nitrogen in summer 2008: a multi-model analysis based on POLMIP
simulations, Atmos. Chem. Phys., 15, 6047–6068, https://doi.org/10.5194/acp-15-6047-2015, 2015.
Aspmo, K., Temme, C., Berg, T., Ferrari, C., Gauchard, P. A., Fain, X., and
Wibetoe, G.: Mercury in the atmosphere, snow and melt water ponds in the
North Atlantic Ocean during Arctic summer, Environ. Sci. Technol., 40, 4083–4089, https://doi.org/10.1021/es052117z, 2006.
Atkinson, H. M., Hughes, C., Shaw, M. J., Roscoe, H. K., Carpenter, L. J., and Liss, P. S.: Halocarbons associated with Arctic sea ice, Deep-Sea Res. Pt. I, 92, 162–175, https://doi.org/10.1016/j.dsr.2014.05.012, 2014.
Backman, J., Schmeisser, L., Virkkula, A., Ogren, J. A., Asmi, E., Starkweather, S., Sharma, S., Eleftheriadis, K., Uttal, T., Jefferson, A.,
Bergin, M., Makshtas, A., Tunved, P., and Fiebig, M.: On Aethalometer measurement uncertainties and an instrument correction factor for the
Arctic, Atmos. Meas. Tech., 10, 5039–5062, https://doi.org/10.5194/amt-10-5039-2017, 2017.
Berg, T., Sekkesæter, S., Steinnes, E., Valdal, A.-K., and Wibetoe, G.:
Springtime depletion of mercury in the European Arctic as observed at Svalbard, Sci. Total Environ., 304, 43–51, https://doi.org/10.1016/S0048-9697(02)00555-7, 2003.
Bognar, K., Zhao, X., Strong, K., Chang, R. Y.-W., Frieß, U., Hayes, P.
L., McClure-Begley, A., Morris, S., Tremblay, S., and Vicente-Luis, A.: Measurements of Tropospheric Bromine Monoxide Over Four Halogen Activation
Seasons in the Canadian High Arctic, J. Geophys. Res.-Atmos., 125, e2020JD033015, https://doi.org/10.1029/2020jd033015, 2020.
Bolton, D.: The Computation of Equivalent Potential Temperature, Mon. Weather Rev., 108, 1046–1053, https://doi.org/10.1175/1520-0493(1980)108<1046:Tcoept>2.0.Co;2, 1980.
Böttcher, K., Paunu, V.-V., Kupiainen, K., Zhizhin, M., Matveev, A., Savolahti, M., Klimont, Z., Väätäinen, S., Lamberg, H., and
Karvosenoja, N.: Black carbon emissions from flaring in Russia in the period 2012–2017, Atmos. Environ., 254, 118390, https://doi.org/10.1016/j.atmosenv.2021.118390, 2021.
Brooks, I. M., Tjernström, M., Persson, P. O. G., Shupe, M. D., Atkinson, R. A., Canut, G., Birch, C. E., Mauritsen, T., Sedlar, J., and Brooks, B. J.: The Turbulent Structure of the Arctic Summer Boundary Layer During The Arctic Summer Cloud-Ocean Study, J. Geophys. Res.-Atmos., 122, 9685–9704, https://doi.org/10.1002/2017JD027234, 2017.
Brooks, S., Arimoto, R., Lindberg, S., and Southworth, G.: Antarctic polar
plateau snow surface conversion of deposited oxidized mercury to gaseous
elemental mercury with fractional long-term burial, Atmos. Environ., 42, 2877–2884, https://doi.org/10.1016/j.atmosenv.2007.05.029, 2008.
Brooks, S., Moore, C., Lew, D., Lefer, B., Huey, G., and Tanner, D.: Temperature and sunlight controls of mercury oxidation and deposition atop
the Greenland ice sheet, Atmos. Chem. Phys., 11, 8295–8306,
https://doi.org/10.5194/acp-11-8295-2011, 2011.
Brooks, S. B., Saiz-Lopez, A., Skov, H., Lindberg, S. E., Plane, J. M. C., and Goodsite, M. E.: The mass balance of mercury in the springtime arctic
environment, Geophys. Res. Lett., 33, L13812, https://doi.org/10.1029/2005gl025525, 2006.
Browse, J., Carslaw, K. S., Arnold, S. R., Pringle, K., and Boucher, O.: The
scavenging processes controlling the seasonal cycle in Arctic sulphate and
black carbon aerosol, Atmos. Chem. Phys., 12, 6775–6798,
https://doi.org/10.5194/acp-12-6775-2012, 2012.
Burd, J. A., Peterson, P. K., Nghiem, S. V., Perovich, D. K., and Simpson, W. R.: Snowmelt onset hinders bromine monoxide heterogeneous recycling in the Arctic, J. Geophys. Res.-Atmos., 122, 8297–8309, https://doi.org/10.1002/2017jd026906, 2017.
Calvert, J. G. and Lindberg, S. E.: Mechanisms of mercury removal by O3 and OH in the atmosphere, Atmos. Environ., 39, 3355–3367, https://doi.org/10.1016/j.atmosenv.2005.01.055, 2005.
Cavalieri, D. J., Parkinson, C. L., Gloersen, P., and Zwally, H. J.: Sea Ice
Concentrations from Nimbus-7 SMMR and DMSP SSM/I-SSMIS Passive Microwave
Data, Version 1, https://doi.org/10.5067/8GQ8LZQVL0VL, 1996.
Christensen, J. H., Brandt, J., Frohn, L. M., and Skov, H.: Modelling of Mercury in the Arctic with the Danish Eulerian Hemispheric Model, Atmos. Chem. Phys., 4, 2251–2257, https://doi.org/10.5194/acp-4-2251-2004, 2004.
Cole, A. S. and Steffen, A.: Trends in long-term gaseous mercury observations in the Arctic and effects of temperature and other atmospheric conditions, Atmos. Chem. Phys., 10, 4661–4672, https://doi.org/10.5194/acp-10-4661-2010, 2010.
Comiso, J. C.: Large Decadal Decline of the Arctic Multiyear Ice Cover, J. Climate, 25, 1176–1193, https://doi.org/10.1175/jcli-d-11-00113.1, 2012.
Croft, B., Martin, R. V., Leaitch, W. R., Tunved, P., Breider, T. J., D'Andrea, S. D., and Pierce, J. R.: Processes controlling the annual cycle of Arctic aerosol number and size distributions, Atmos. Chem. Phys., 16, 3665–3682, https://doi.org/10.5194/acp-16-3665-2016, 2016.
Dastoor, A. P. and Durnford, D. A.: Arctic Ocean: Is It a Sink or a Source of Atmospheric Mercury?, Environ. Sci. Technol., 48, 1707–1717, https://doi.org/10.1021/es404473e, 2014.
Dastoor, A. P., Davignon, D., Theys, N., Van Roozendael, M., Steffen, A., and Ariya, P. A.: Modeling Dynamic Exchange of Gaseous Elemental Mercury at Polar Sunrise, Environ. Sci. Technol., 42, 5183–5188, https://doi.org/10.1021/es800291w, 2008.
Dibb, J. E., Arsenault, M., Peterson, M. C., and Honrath, R. E.: Fast nitrogen oxide photochemistry in Summit, Greenland snow, Atmos. Environ., 36, 2501–2511, https://doi.org/10.1016/s1352-2310(02)00130-9, 2002.
Dibble, T. S., Zelie, M. J., and Mao, H.: Thermodynamics of reactions of ClHg and BrHg radicals with atmospherically abundant free radicals, Atmos. Chem. Phys., 12, 10271–10279, https://doi.org/10.5194/acp-12-10271-2012, 2012.
DiMento, B. P., Mason, R. P., Brooks, S., and Moore, C.: The impact of sea
ice on the air-sea exchange of mercury in the Arctic Ocean, Deep-Sea Res. Pt. I, 144, 28–38, https://doi.org/10.1016/j.dsr.2018.12.001, 2019.
Donohoue, D. L., Bauer, D., Cossairt, B., and Hynes, A. J.: Temperature and
Pressure Dependent Rate Coefficients for the Reaction of Hg with Br and the
Reaction of Br with Br: A Pulsed Laser Photolysis-Pulsed Laser Induced
Fluorescence Study, J. Phys. Chem. A, 110, 6623–6632,
https://doi.org/10.1021/jp054688j, 2006.
Douglas, T. A. and Blum, J. D.: Mercury Isotopes Reveal Atmospheric Gaseous
Mercury Deposition Directly to the Arctic Coastal Snowpack, Environ. Sci. Technol. Lett., 6, 235–242, https://doi.org/10.1021/acs.estlett.9b00131, 2019.
Douglas, T. A., Sturm, M., Blum, J. D., Polashenski, C., Stuefer, S.,
Hiemstra, C., Steffen, A., Filhol, S., and Prevost, R.: A Pulse of Mercury
and Major Ions in Snowmelt Runoff from a Small Arctic Alaska Watershed,
Environ. Sci. Technol., 51, 11145–11155, https://doi.org/10.1021/acs.est.7b03683, 2017.
Draxler, R. R. and Hess, G. D.: An overview of the HYSPLIT_4 modelling system for trajectories, dispersion and deposition, Aust. Meteorol. Mag., 47, 295–308, 1998.
Drinovec, L., Močnik, G., Zotter, P., Prévôt, A. S. H., Ruckstuhl, C., Coz, E., Rupakheti, M., Sciare, J., Müller, T.,
Wiedensohler, A., and Hansen, A. D. A.: The “dual-spot” Aethalometer: an
improved measurement of aerosol black carbon with real-time loading compensation, Atmos. Meas. Tech., 8, 1965–1979, https://doi.org/10.5194/amt-8-1965-2015, 2015.
Durnford, D. and Dastoor, A.: The behavior of mercury in the cryosphere: A
review of what we know from observations, J. Geophys. Res., 116, D06305, https://doi.org/10.1029/2010jd014809, 2011.
Dusek, U., Reischl, G. P., and Hitzenberger, R.: CCN Activation of Pure and
Coated Carbon Black Particles, Environ. Sci. Technol., 40, 1223–1230, https://doi.org/10.1021/es0503478, 2006.
Faïn, X., Obrist, D., Hallar, A. G., McCubbin, I., and Rahn, T.: High
levels of reactive gaseous mercury observed at a high elevation research
laboratory in the Rocky Mountains, Atmos. Chem. Phys., 9, 8049–8060,
https://doi.org/10.5194/acp-9-8049-2009, 2009.
Flannigan, M., Stocks, B., Turetsky, M., and Wotton, M.: Impacts of climate
change on fire activity and fire management in the circumboreal forest, Global Change Biol., 15, 549–560, https://doi.org/10.1111/j.1365-2486.2008.01660.x, 2009.
Freud, E., Krejci, R., Tunved, P., Leaitch, R., Nguyen, Q. T., Massling, A.,
Skov, H., and Barrie, L.: Pan-Arctic aerosol number size distributions:
seasonality and transport patterns, Atmos. Chem. Phys., 17, 8101–8128,
https://doi.org/10.5194/acp-17-8101-2017, 2017.
Frey, M. M., Norris, S. J., Brooks, I. M., Anderson, P. S., Nishimura, K.,
Yang, X., Jones, A. E., Nerentorp Mastromonaco, M. G., Jones, D. H., and Wolff, E. W.: First direct observation of sea salt aerosol production from
blowing snow above sea ice, Atmos. Chem. Phys., 20, 2549–2578,
https://doi.org/10.5194/acp-20-2549-2020, 2020.
Friedli, H. R., Radke, L. F., Lu, J. Y., Banic, C. M., Leaitch, W. R., and
MacPherson, J. I.: Mercury emissions from burning of biomass from temperate
North American forests: laboratory and airborne measurements, Atmos. Environ., 37, 253–267, https://doi.org/10.1016/S1352-2310(02)00819-1, 2003.
Friedli, H. R., Arellano, A. F., Cinnirella, S., and Pirrone, N.: Initial
Estimates of Mercury Emissions to the Atmosphere from Global Biomass Burning, Environ. Sci. Technol., 43, 3507–3513, https://doi.org/10.1021/es802703g, 2009.
Fu, X., Marusczak, N., Heimbürger, L. E., Sauvage, B., Gheusi, F., Prestbo, E. M., and Sonke, J. E.: Atmospheric mercury speciation dynamics at
the high-altitude Pic du Midi Observatory, southern France, Atmos. Chem.
Phys., 16, 5623–5639, https://doi.org/10.5194/acp-16-5623-2016, 2016.
Giordano, M. R., Kalnajs, L. E., Goetz, J. D., Avery, A. M., Katz, E., May, N. W., Leemon, A., Mattson, C., Pratt, K. A., and DeCarlo, P. F.: The importance of blowing snow to halogen-containing aerosol in coastal Antarctica: influence of source region versus wind speed, Atmos. Chem.
Phys., 18, 16689–16711, https://doi.org/10.5194/acp-18-16689-2018, 2018.
Goodsite, M. E., Plane, J. M. C., and Skov, H.: A theoretical study of the
oxidation of Hg0 to HgBr2 in the troposphere, Environ. Sci. Technol., 38, 1772–1776, https://doi.org/10.1021/es034680s, 2004.
Goodsite, M. E., Plane, J. M. C., and Skov, H.: Correction to A Theoretical
Study of the Oxidation of Hg0 to HgBr2 in the Troposphere, Environ. Sci. Technol., 46, 5262–5262, https://doi.org/10.1021/es301201c, 2012.
Gratz, L. E., Ambrose, J. L., Jaffe, D. A., Shah, V., Jaegle, L., Stutz, J.,
Festa, J., Spolaor, M., Tsai, C., Selin, N. E., Song, S., Zhou, X., Weinheimer, A. J., Knapp, D. J., Montzka, D. D., Flocke, F. M., Campos, T.
L., Apel, E., Hornbrook, R., Blake, N. J., Hall, S., Tyndall, G. S., Reeves,
M., Stechman, D., and Stell, M.: Oxidation of mercury by bromine in the
subtropical Pacific free troposphere, Geophys. Res. Lett., 42, 10494–10502, https://doi.org/10.1002/2015gl066645, 2015.
Greene, C. A.: Arctic Sea ice, available at: https://www.mathworks.com/matlabcentral/fileexchange/56923-arctic-sea-ice,
last access: 26 January 2020.
Greene, C. A., Gwyther, D. E., and Blankenship, D. D.: Antarctic Mapping Tools for MATLAB, Comput. Geosci., 104, 151–157, https://doi.org/10.1016/j.cageo.2016.08.003, 2017.
Gustin, M. S., Amos, H. M., Huang, J., Miller, M. B., and Heidecorn, K.:
Measuring and modeling mercury in the atmosphere: a critical review, Atmos.
Chem. Phys., 15, 5697–5713, https://doi.org/10.5194/acp-15-5697-2015, 2015.
Gustin, M. S., Dunham-Cheatham, S. M., Huang, J., Lindberg, S., and Lyman, S. N.: Development of an Understanding of Reactive Mercury in Ambient Air: A
Review, Atmosphere, 12, 73, https://doi.org/10.3390/atmos12010073, 2021.
Halfacre, J. W., Shepson, P. B., and Pratt, K. A.: pH-dependent production of molecular chlorine, bromine, and iodine from frozen saline surfaces, Atmos. Chem. Phys., 19, 4917–4931, https://doi.org/10.5194/acp-19-4917-2019, 2019.
Hara, K., Osada, K., Yabuki, M., Takashima, H., Theys, N., and Yamanouchi, T.: Important contributions of sea-salt aerosols to atmospheric bromine cycle in the Antarctic coasts, Scient. Rep., 8, 13852, https://doi.org/10.1038/s41598-018-32287-4, 2018.
Helmig, D., Oltmans, S. J., Carlson, D., Lamarque, J.-F., Jones, A., Labuschagne, C., Anlauf, K., and Hayden, K.: A review of surface ozone in the polar regions, Atmos. Environ., 41, 5138–5161, https://doi.org/10.1016/j.atmosenv.2006.09.053, 2007.
Hirdman, D., Aspmo, K., Burkhart, J. F., Eckhardt, S., Sodemann, H., and Stohl, A.: Transport of mercury in the Arctic atmosphere: Evidence for a spring-time net sink and summer-time source, Geophys. Res. Lett., 36, L12814, https://doi.org/10.1029/2009gl038345, 2009.
Holmes, C. D., Jacob, D. J., and Yang, X.: Global lifetime of elemental mercury against oxidation by atomic bromine in the free troposphere, Geophys. Res. Lett., 33, L20808, https://doi.org/10.1029/2006gl027176, 2006.
Holmes, C. D., Jacob, D. J., Corbitt, E. S., Mao, J., Yang, X., Talbot, R., and Slemr, F.: Global atmospheric model for mercury including oxidation by
bromine atoms, Atmos. Chem. Phys., 10, 12037–12057, https://doi.org/10.5194/acp-10-12037-2010, 2010.
Horowitz, H. M., Jacob, D. J., Zhang, Y., Dibble, T. S., Slemr, F., Amos, H.
M., Schmidt, J. A., Corbitt, E. S., Marais, E. A., and Sunderland, E. M.: A
new mechanism for atmospheric mercury redox chemistry: implications for the
global mercury budget, Atmos. Chem. Phys., 17, 6353–6371,
https://doi.org/10.5194/acp-17-6353-2017, 2017.
Huang, J. and Gustin, M. S.: Uncertainties of Gaseous Oxidized Mercury Measurements Using KCl-Coated Denuders, Cation-Exchange Membranes, and Nylon
Membranes: Humidity Influences, Environ. Sci. Technol., 49, 6102–6108, https://doi.org/10.1021/acs.est.5b00098, 2015.
Huang, J., Miller, M. B., Edgerton, E., and Sexauer Gustin, M.: Deciphering
potential chemical compounds of gaseous oxidized mercury in Florida, USA,
Atmos. Chem. Phys., 17, 1689–1698, https://doi.org/10.5194/acp-17-1689-2017, 2017.
Huang, K., Fu, J. S., Prikhodko, V. Y., Storey, J. M., Romanov, A., Hodson,
E. L., Cresko, J., Morozova, I., Ignatieva, Y., and Cabaniss, J.: Russian
anthropogenic black carbon: Emission reconstruction and Arctic black carbon
simulation, J. Geophys. Res.-Atmos., 120, 11306–11333, https://doi.org/10.1002/2015JD023358, 2015.
Hynes, A. J., Donohoue, D. L., Goodsite, M. E., and Hedgecock, I. M.: Our
current understanding of major chemical and physical processes affecting mercury dynamics in the atmosphere and at the air-water/terrestrial interfaces, in: Mercury Fate and Transport in the Global Atmosphere: Emissions, Measurements and Models, edited by: Mason, R. and Pirrone, N.,
Springer US, Boston, MA, 427–457, 2009.
Igel, A. L., Ekman, A. M. L., Leck, C., Tjernström, M., Savre, J., and
Sedlar, J.: The free troposphere as a potential source of arctic boundary layer aerosol particles, Geophys. Res. Lett., 44, 7053–7060,
https://doi.org/10.1002/2017gl073808, 2017.
Jacob, D. J., Crawford, J. H., Maring, H., Clarke, A. D., Dibb, J. E., Emmons, L. K., Ferrare, R. A., Hostetler, C. A., Russell, P. B., Singh, H.
B., Thompson, A. M., Shaw, G. E., McCauley, E., Pederson, J. R., and Fisher, J. A.: The Arctic Research of the Composition of the Troposphere from Aircraft and Satellites (ARCTAS) mission: design, execution, and first results, Atmos. Chem. Phys., 10, 5191–5212, https://doi.org/10.5194/acp-10-5191-2010, 2010.
Jiang, S., Ye, A., and Xiao, C.: The temperature increase in Greenland has
accelerated in the past five years, Global Planet. Change, 194, 103297, https://doi.org/10.1016/j.gloplacha.2020.103297, 2020.
Jiao, Y. and Dibble, T. S.: Quality Structures, Vibrational Frequencies, and Thermochemistry of the Products of Reaction of BrHg with NO2, HO2, ClO, BrO, and IO, J. Phys. Chem. A, 119, 10502–10510,
https://doi.org/10.1021/acs.jpca.5b04889, 2015.
Jiao, Y. and Dibble, T. S.: First kinetic study of the atmospherically important reactions BrHgy+NO2 and BrHgy+HOO, Phys. Chem. Chem. Phys., 19, 1826–1838, https://doi.org/10.1039/C6CP06276H, 2017a.
Jiao, Y. and Dibble, T. S.: Structures, Vibrational Frequencies, and Bond Energies of the BrHgOX and BrHgXO Species Formed in Atmospheric Mercury
Depletion Events, J. Phys. Chem. A, 121, 7976–7985,
https://doi.org/10.1021/acs.jpca.7b06829, 2017b.
Jiskra, M., Sonke, J. E., Agnan, Y., Helmig, D., and Obrist, D.: Insights from mercury stable isotopes on terrestrial–atmosphere exchange of Hg(0) in the Arctic tundra, Biogeosciences, 16, 4051–4064, https://doi.org/10.5194/bg-16-4051-2019, 2019.
Kaleschke, L., Richter, A., Burrows, J., Afe, O., Heygster, G., Notholt, J.,
Rankin, A. M., Roscoe, H. K., Hollwedel, J., Wagner, T., and Jacobi, H. W.:
Frost flowers on sea ice as a source of sea salt and their influence on
tropospheric halogen chemistry, Geophys. Res. Lett., 31, L16114, https://doi.org/10.1029/2004gl020655, 2004.
Kamp, J., Skov, H., Jensen, B., and Sorensen, L. L.: Fluxes of gaseous elemental mercury (GEM) in the High Arctic during atmospheric mercury depletion events (AMDEs), Atmos. Chem. Phys., 18, 6923–6938,
https://doi.org/10.5194/acp-18-6923-2018, 2018.
Kelly, R., Chipman, M. L., Higuera, P. E., Stefanova, I., Brubaker, L. B.,
and Hu, F. S.: Recent burning of boreal forests exceeds fire regime limits of the past 10,000 years, P. Natl. Acad. Sci. USA, 110, 13055–13060, https://doi.org/10.1073/pnas.1305069110, 2013.
Lampert, A., Maturilli, M., Ritter, C., Hoffmann, A., Stock, M., Herber, A.,
Birnbaum, G., Neuber, R., Dethloff, K., Orgis, T., Stone, R., Brauner, R.,
Kässbohrer, J., Haas, C., Makshtas, A., Sokolov, V., and Liu, P.: The
Spring-Time Boundary Layer in the Central Arctic Observed during PAMARCMiP 2009, Atmosphere, 3, 320–351, 2012.
Landis, M. S., Stevens, R. K., Schaedlich, F., and Prestbo, E. M.: Development and characterization of an annular denuder methodology for the
measurement of divalent inorganic reactive gaseous mercury in ambient air,
Environ. Sci. Technol., 36, 3000–3009, https://doi.org/10.1021/es015887t, 2002.
Laurier, F. J. G.: Reactive gaseous mercury formation in the North Pacific
Ocean's marine boundary layer: A potential role of halogen chemistry, J. Geophys. Res., 108, 4529, https://doi.org/10.1029/2003jd003625, 2003.
Law, K. S., Stohl, A., Quinn, P. K., Brock, C. A., Burkhart, J. F., Paris,
J.-D., Ancellet, G., Singh, H. B., Roiger, A., Schlager, H., Dibb, J., Jacob, D. J., Arnold, S. R., Pelon, J., and Thomas, J. L.: Arctic Air Pollution: New Insights from POLARCAT-IPY, B. Am. Meteorol. Soc., 95, 1873–1895, https://doi.org/10.1175/bams-d-13-00017.1, 2014.
Lin, C.-J. and Pehkonen, S. O.: Oxidation of elemental mercury by aqueous
chlorine (
Lindberg, S. E., Brooks, S., Lin, C. J., Scott, K. J., Landis, M. S., Stevens, R. K., Goodsite, M., and Richter, A.: Dynamic oxidation of gaseous
mercury in the Arctic troposphere at polar sunrise, Environ. Sci. Technol., 36, 1245–1256, https://doi.org/10.1021/es0111941, 2002.
Lu, J. Y., Schroeder, W. H., Barrie, L. A., Steffen, A., Welch, H. E.,
Martin, K., Lockhart, L., Hunt, R. V., Boila, G., and Richter, A.: Magnification of atmospheric mercury deposition to polar regions in
springtime: The link to tropospheric ozone depletion chemistry, Geophys. Res. Lett., 28, 3219–3222, https://doi.org/10.1029/2000gl012603, 2001.
Lyman, S. N., Cheng, I., Gratz, L. E., Weiss-Penzias, P., and Zhang, L.: An
updated review of atmospheric mercury, Sci. Total Environ., 707, 135575, https://doi.org/10.1016/j.scitotenv.2019.135575, 2020.
Macdonald, R. W. and Loseto, L. L.: Are Arctic Ocean ecosystems exceptionally vulnerable to global emissions of mercury? A call for emphasised research on methylation and the consequences of climate change, Environ. Chem., 7, 133–138, https://doi.org/10.1071/en09127, 2010.
Marusczak, N., Sonke, J. E., Fu, X., and Jiskra, M.: Tropospheric GOM at the
Pic du Midi Observatory – Correcting Bias in Denuder Based Observations,
Environ. Sci. Technol., 51, 863–869, https://doi.org/10.1021/acs.est.6b04999, 2017.
Møller, A. K., Barkay, T., Al-Soud, W. A., Sørensen, S. J., Skov, H.,
and Kroer, N.: Diversity and characterization of mercury-resistant bacteria
in snow, freshwater and sea-ice brine from the High Arctic, FEMS Microbiol. Ecol., 75, 390–401, https://doi.org/10.1111/j.1574-6941.2010.01016.x, 2011.
Monks, S. A., Arnold, S. R., Emmons, L. K., Law, K. S., Turquety, S., Duncan, B. N., Flemming, J., Huijnen, V., Tilmes, S., Langner, J., Mao, J., Long, Y., Thomas, J. L., Steenrod, S. D., Raut, J. C., Wilson, C., Chipperfield, M. P., Diskin, G. S., Weinheimer, A., Schlager, H., and Ancellet, G.: Multi-model study of chemical and physical controls on transport of anthropogenic and biomass burning pollution to the Arctic, Atmos. Chem. Phys., 15, 3575–3603, https://doi.org/10.5194/acp-15-3575-2015, 2015.
Muntean, M., Janssens-Maenhout, G., Song, S., Giang, A., Selin, N. E., Zhong, H., Zhao, Y., Olivier, J. G. J., Guizzardi, D., Crippa, M., Schaaf, E., and Dentener, F.: Evaluating EDGARv4.tox2 speciated mercury emissions ex-post scenarios and their impacts on modelled global and regional wet deposition patterns, Atmos. Environ., 184, 56–68, https://doi.org/10.1016/j.atmosenv.2018.04.017, 2018.
Nguyen, Q. T., Glasius, M., Sorensen, L. L., Jensen, B., Skov, H., Birmili, W., Wiedensohler, A., Kristensson, A., Nojgaard, J. K., and Massling, A.:
Seasonal variation of atmospheric particle number concentrations, new particle formation and atmospheric oxidation capacity at the high Arctic site Villum Research Station, Station Nord, Atmos. Chem. Phys., 16, 11319–11336, https://doi.org/10.5194/acp-16-11319-2016, 2016.
Obrist, D., Tas, E., Peleg, M., Matveev, V., Faïn, X., Asaf, D., and Luria, M.: Bromine-induced oxidation of mercury in the mid-latitude atmosphere, Nat. Geosci., 4, 22–26, https://doi.org/10.1038/ngeo1018, 2010.
Pal, B. and Ariya, P. A.: Studies of ozone initiated reactions of gaseous mercury: kinetics, product studies, and atmospheric implications, Phys. Chem. Chem. Phys., 6, 572–579, https://doi.org/10.1039/B311150D, 2004.
Park, J.-D. and Zheng, W.: Human Exposure and Health Effects of Inorganic and Elemental Mercury, J. Prev. Med. Publ. Health, 45, 344–352,
https://doi.org/10.3961/jpmph.2012.45.6.344, 2012.
Peterson, P. K., Pöhler, D., Sihler, H., Zielcke, J., General, S., Frieß, U., Platt, U., Simpson, W. R., Nghiem, S. V., Shepson, P. B., Stirm, B. H., Dhaniyala, S., Wagner, T., Caulton, D. R., Fuentes, J. D., and
Pratt, K. A.: Observations of bromine monoxide transport in the Arctic
sustained on aerosol particles, Atmos. Chem. Phys., 17, 7567–7579,
https://doi.org/10.5194/acp-17-7567-2017, 2017.
Peterson, P. K., Pöhler, D., Zielcke, J., General, S., Frieß, U.,
Platt, U., Simpson, W. R., Nghiem, S. V., Shepson, P. B., Stirm, B. H., and
Pratt, K. A.: Springtime Bromine Activation over Coastal and Inland Arctic
Snowpacks, ACS Earth Space Chem., 2, 1075–1086,
https://doi.org/10.1021/acsearthspacechem.8b00083, 2018.
Peterson, P. K., Hartwig, M., May, N. W., Schwartz, E., Rigor, I., Ermold, W., Steele, M., Morison, J. H., Nghiem, S. V., and Pratt, K. A.: Snowpack measurements suggest role for multi-year sea ice regions in Arctic atmospheric bromine and chlorine chemistry, Elem.-Sci. Anth., 7, 14, https://doi.org/10.1525/elementa.352, 2019.
Pfaffhuber, K. A., Berg, T., Hirdman, D., and Stohl, A.: Atmospheric mercury
observations from Antarctica: seasonal variation and source and sink region
calculations, Atmos. Chem. Phys., 12, 3241–3251, https://doi.org/10.5194/acp-12-3241-2012, 2012.
Pirrone, N., Cinnirella, S., Feng, X., Finkelman, R. B., Friedli, H. R.,
Leaner, J., Mason, R., Mukherjee, A. B., Stracher, G. B., Streets, D. G., and Telmer, K.: Global mercury emissions to the atmosphere from anthropogenic and natural sources, Atmos. Chem. Phys., 10, 5951–5964, https://doi.org/10.5194/acp-10-5951-2010, 2010.
Reid, J. S., Koppmann, R., Eck, T. F., and Eleuterio, D. P.: A review of
biomass burning emissions part II: intensive physical properties of biomass
burning particles, Atmos. Chem. Phys., 5, 799–825, https://doi.org/10.5194/acp-5-799-2005, 2005.
Rolph, G., Stein, A., and Stunder, B.: Real-time Environmental Applications
and Display sYstem: READY, Environ. Model. Softw., 95, 210–228, https://doi.org/10.1016/j.envsoft.2017.06.025, 2017.
Saiz-Lopez, A., Travnikov, O., Sonke, J. E., Thackray, C. P., Jacob, D. J.,
Carmona-García, J., Francés-Monerris, A., Roca-Sanjuán, D.,
Acuña, A. U., Dávalos, J. Z., Cuevas, C. A., Jiskra, M., Wang, F.,
Bieser, J., Plane, J. M. C., and Francisco, J. S.: Photochemistry of oxidized Hg(I) and Hg(II) species suggests missing mercury oxidation in the
troposphere, P. Natl. Acad. Sci. USA, 117, 30949–30956, https://doi.org/10.1073/pnas.1922486117, 2020.
Sander, R.: Compilation of Henry's law constants (version 4.0) for water as
solvent, Atmos. Chem. Phys., 15, 4399–4981, https://doi.org/10.5194/acp-15-4399-2015, 2015.
Schacht, J., Heinold, B., Quaas, J., Backman, J., Cherian, R., Ehrlich, A.,
Herber, A., Huang, W. T. K., Kondo, Y., Massling, A., Sinha, P. R., Weinzierl, B., Zanatta, M., and Tegen, I.: The importance of the representation of air pollution emissions for the modeled distribution and
radiative effects of black carbon in the Arctic, Atmos. Chem. Phys., 19,
11159–11183, https://doi.org/10.5194/acp-19-11159-2019, 2019.
Schmeisser, L., Backman, J., Ogren, J. A., Andrews, E., Asmi, E., Starkweather, S., Uttal, T., Fiebig, M., Sharma, S., Eleftheriadis, K., Vratolis, S., Bergin, M., Tunved, P., and Jefferson, A.: Seasonality of
aerosol optical properties in the Arctic, Atmos. Chem. Phys., 18, 11599–11622, https://doi.org/10.5194/acp-18-11599-2018, 2018.
Schmeissner, T., Krejci, R., Ström, J., Birmili, W., Wiedensohler, A.,
Hochschild, G., Gross, J., Hoffmann, P., and Calderon, S.: Analysis of number size distributions of tropical free tropospheric aerosol particles observed at Pico Espejo (4765 m a.s.l.), Venezuela, Atmos. Chem. Phys., 11, 3319–3332, https://doi.org/10.5194/acp-11-3319-2011, 2011.
Schroeder, W., Oliva, P., Giglio, L., and Csiszar, I. A.: The New VIIRS 375 m active fire detection data product: Algorithm description and initial
assessment, Remote Sens. Environ., 143, 85–96, https://doi.org/10.1016/j.rse.2013.12.008, 2014.
Schroeder, W. H., Anlauf, K. G., Barrie, L. A., Lu, J. Y., Steffen, A., Schneeberger, D. R., and Berg, T.: Arctic springtime depletion of mercury,
Nature, 394, 331–332, https://doi.org/10.1038/28530, 1998.
Schulz, H., Zanatta, M., Bozem, H., Leaitch, W. R., Herber, A. B., Burkart, J., Willis, M. D., Kunkel, D., Hoor, P. M., Abbatt, J. P. D., and Gerdes, R.: High Arctic aircraft measurements characterising black carbon vertical variability in spring and summer, Atmos. Chem. Phys., 19, 2361–2384,
https://doi.org/10.5194/acp-19-2361-2019, 2019.
Semane, N., Peuch, V. H., El Amraoui, L., Bencherif, H., Massart, S., Cariolle, D., Attie, J. L., and Abida, R.: An observed and analysed stratospheric ozone intrusion over the high Canadian Arctic UTLS region
during the summer of 2003, Q. J. Roy. Meteorol. Soc., 133, 171–178, https://doi.org/10.1002/qj.141, 2007.
Shah, V. and Jaeglé, L.: Subtropical subsidence and surface deposition of oxidized mercury produced in the free troposphere, Atmos. Chem. Phys., 17, 8999–9017, https://doi.org/10.5194/acp-17-8999-2017, 2017.
Shepler, B. C., Balabanov, N. B., and Peterson, K. A.: Hg + BrHgBr
recombination and collision-induced dissociation dynamics, J. Chem. Phys., 127, 164304, https://doi.org/10.1063/1.2777142, 2007.
Simpson, W. R., Brown, S. S., Saiz-Lopez, A., Thornton, J. A., and Glasow, R.: Tropospheric halogen chemistry: sources, cycling, and impacts, Chem. Rev., 115, 4035–4062, https://doi.org/10.1021/cr5006638, 2015.
Simpson, W. R., Peterson, P. K., Frieß, U., Sihler, H., Lampel, J., Platt, U., Moore, C., Pratt, K., Shepson, P., Halfacre, J., and Nghiem, S. V.: Horizontal and vertical structure of reactive bromine events probed by
bromine monoxide MAX-DOAS, Atmos. Chem. Phys., 17, 9291–9309,
https://doi.org/10.5194/acp-17-9291-2017, 2017.
Skov, H., Christensen, J. H., Goodsite, M. E., Heidam, N. Z., Jensen, B., Wahlin, P., and Geernaert, G.: Fate of elemental mercury in the arctic during atmospheric mercury depletion episodes and the load of atmospheric mercury to the arctic, Environ. Sci. Technol., 38, 2373–2382, https://doi.org/10.1021/es030080h, 2004.
Skov, H., Brooks, S., Goodsite, M., Lindberg, S., Meyers, T., Landis, M.,
Larsen, M., Jensen, B., McConville, G., and Christensen, J.: Fluxes of reactive gaseous mercury measured with a newly developed method using relaxed eddy accumulation, Atmos. Environ., 40, 5452–5463,
https://doi.org/10.1016/j.atmosenv.2006.04.061, 2006.
Skov, H., Hjorth, J., Nordstrøm, C., Jensen, B., Christoffersen, C., Bech Poulsen, M., Baldtzer Liisberg, J., Beddows, D., Dall'Osto, M., and Christensen, J. H.: Variability in gaseous elemental mercury at Villum Research Station, Station Nord, in North Greenland from 1999 to 2017, Atmos. Chem. Phys., 20, 13253–13265, https://doi.org/10.5194/acp-20-13253-2020, 2020.
Slemr, F., Weigelt, A., Ebinghaus, R., Kock, H. H., Bödewadt, J.,
Brenninkmeijer, C. A. M., Rauthe-Schöch, A., Weber, S., Hermann, M., Becker, J., Zahn, A., and Martinsson, B.: Atmospheric mercury measurements
onboard the CARIBIC passenger aircraft, Atmos. Meas. Tech., 9, 2291–2302,
https://doi.org/10.5194/amt-9-2291-2016, 2016.
Soerensen, A. L., Skov, H., Jacob, D. J., Soerensen, B. T., and Johnson, M.
S.: Global Concentrations of Gaseous Elemental Mercury and Reactive Gaseous
Mercury in the Marine Boundary Layer, Environ. Sci. Technol., 44, 7425–7430, https://doi.org/10.1021/es903839n, 2010.
Sommar, J., Andersson, M. E., and Jacobi, H. W.: Circumpolar measurements of
speciated mercury, ozone and carbon monoxide in the boundary layer of the
Arctic Ocean, Atmos. Chem. Phys., 10, 5031–5045, https://doi.org/10.5194/acp-10-5031-2010, 2010.
Steen, A. O., Berg, T., Dastoor, A. P., Durnford, D. A., Engelsen, O., Hole,
L. R., and Pfaffhuber, K. A.: Natural and anthropogenic atmospheric mercury in the European Arctic: a fractionation study, Atmos. Chem. Phys., 11, 6273–6284, https://doi.org/10.5194/acp-11-6273-2011, 2011.
Steffen, A., Schroeder, W., Bottenheim, J., Narayan, J., and Fuentes, J. D.:
Atmospheric mercury concentrations: measurements and profiles near snow and
ice surfaces in the Canadian Arctic during Alert 2000, Atmos. Environ., 36, 2653–2661, https://doi.org/10.1016/S1352-2310(02)00112-7, 2002.
Steffen, A., Bottenheim, J., Cole, A., Ebinghaus, R., Lawson, G., and Leaitch, W. R.: Atmospheric mercury speciation and mercury in snow over time
at Alert, Canada, Atmos. Chem. Phys., 14, 2219–2231, https://doi.org/10.5194/acp-14-2219-2014, 2014.
Steffen, A., Lehnherr, I., Cole, A., Ariya, P., Dastoor, A., Durnford, D.,
Kirk, J., and Pilote, M.: Atmospheric mercury in the Canadian Arctic. Part I: a review of recent field measurements, Sci. Total Environ., 509–510, 3–15,
https://doi.org/10.1016/j.scitotenv.2014.10.109, 2015.
Stephens, C. R., Shepson, P. B., Steffen, A., Bottenheim, J. W., Liao, J.,
Huey, L. G., Apel, E., Weinheimer, A., Hall, S. R., Cantrell, C., Sive, B.
C., Knapp, D. J., Montzka, D. D., and Hornbrook, R. S.: The relative importance of chlorine and bromine radicals in the oxidation of atmospheric
mercury at Barrow, Alaska, J. Geophys. Res.-Atmos., 117, D00R11, https://doi.org/10.1029/2011jd016649, 2012.
Stern, G. A., Macdonald, R. W., Outridge, P. M., Wilson, S., Chetelat, J.,
Cole, A., Hintelmann, H., Loseto, L. L., Steffen, A., Wang, F., and Zdanowicz, C.: How does climate change influence Arctic mercury?, Sci. Total
Environ., 414, 22–42, https://doi.org/10.1016/j.scitotenv.2011.10.039, 2012.
Stohl, A.: Computation, accuracy and applications of trajectories – A review
and bibliography, Atmos. Environ., 32, 947–966, https://doi.org/10.1016/s1352-2310(97)00457-3, 1998.
Stohl, A.: Characteristics of atmospheric transport into the Arctic troposphere, J. Geophys. Res., 111, D11306, https://doi.org/10.1029/2005jd006888, 2006.
Stroeve, J. C., Serreze, M. C., Holland, M. M., Kay, J. E., Malanik, J., and
Barrett, A. P.: The Arctic's rapidly shrinking sea ice cover: a research
synthesis, Climatic Change, 110, 1005–1027, https://doi.org/10.1007/s10584-011-0101-1, 2012.
Sturges, W. T., Cota, G. F., and Buckley, P. T.: Bromoform emission from
Arctic ice algae, Nature, 358, 660–662, https://doi.org/10.1038/358660a0, 1992.
Swartzendruber, P. C., Jaffe, D. A., Prestbo, E. M., Weiss-Penzias, P., Selin, N. E., Park, R., Jacob, D. J., Strode, S., and Jaeglé, L.:
Observations of reactive gaseous mercury in the free troposphere at the
Mount Bachelor Observatory, J. Geophys. Res., 111, D24301, https://doi.org/10.1029/2006jd007415, 2006.
Talbot, R., Mao, H., Scheuer, E., Dibb, J., and Avery, M.: Total depletion
of Hg degrees in the upper troposphere-lower stratosphere, Geophys. Res. Lett., 34, L23804, https://doi.org/10.1029/2007gl031366, 2007.
Tarasick, D. W. and Bottenheim, J. W.: Surface ozone depletion episodes in
the Arctic and Antarctic from historical ozonesonde records, Atmos. Chem.
Phys., 2, 197–205, https://doi.org/10.5194/acp-2-197-2002, 2002.
Thomas, J. L., Dibb, J. E., Huey, L. G., Liao, J., Tanner, D., Lefer, B.,
von Glasow, R., and Stutz, J.: Modeling chemistry in and above snow at
Summit, Greenland – Part 2: Impact of snowpack chemistry on the oxidation
capacity of the boundary layer, Atmos. Chem. Phys., 12, 6537–6554,
https://doi.org/10.5194/acp-12-6537-2012, 2012.
Toyota, K., Dastoor, A. P., and Ryzhkov, A.: Air–snowpack exchange of bromine, ozone and mercury in the springtime Arctic simulated by the 1-D
model PHANTAS – Part 2: Mercury and its speciation, Atmos. Chem. Phys., 14, 4135–4167, https://doi.org/10.5194/acp-14-4135-2014, 2014.
Tunved, P., Ström, J., and Krejci, R.: Arctic aerosol life cycle: linking aerosol size distributions observed between 2000 and 2010 with air mass transport and precipitation at Zeppelin station, Ny-Ålesund, Svalbard, Atmos. Chem. Phys., 13, 3643–3660, https://doi.org/10.5194/acp-13-3643-2013, 2013.
UNEP: UNEP: Minamata Convention on Mercury, available at:
http://www.mercuryconvention.org/Convention/tabid/3426/Default.aspx (last access: 12 November 2020), 2013.
von Glasow, R.: Atmospheric chemistry in volcanic plumes, P. Natl. Acad. Sci. USA, 107, 6594–6599, https://doi.org/10.1073/pnas.0913164107, 2010.
Walker, T. W., Jones, D. B. A., Parrington, M., Henze, D. K., Murray, L. T.,
Bottenheim, J. W., Anlauf, K., Worden, J. R., Bowman, K. W., Shim, C., Singh, K., Kopacz, M., Tarasick, D. W., Davies, J., von der Gathen, P., Thompson, A. M., and Carouge, C. C.: Impacts of midlatitude precursor emissions and local photochemistry on ozone abundances in the Arctic, J. Geophys. Res.-Atmos., 117, D01305, https://doi.org/10.1029/2011jd016370, 2012.
Wang, S., McNamara, S. M., Moore, C. W., Obrist, D., Steffen, A., Shepson, P. B., Staebler, R. M., Raso, A. R. W., and Pratt, K. A.: Direct detection of atmospheric atomic bromine leading to mercury and ozone depletion, P. Natl. Acad. Sci. USA, 116, 14479–14484, https://doi.org/10.1073/pnas.1900613116, 2019.
Weingartner, E., Saathoff, H., Schnaiter, M., Streit, N., Bitnar, B., and
Baltensperger, U.: Absorption of light by soot particles: determination of the absorption coefficient by means of aethalometers, J. Aerosol Sci., 34, 1445–1463, https://doi.org/10.1016/S0021-8502(03)00359-8, 2003.
Weiss-Penzias, P., Amos, H. M., Selin, N. E., Gustin, M. S., Jaffe, D. A.,
Obrist, D., Sheu, G. R., and Giang, A.: Use of a global model to understand
speciated atmospheric mercury observations at five high-elevation sites,
Atmos. Chem. Phys., 15, 1161–1173, https://doi.org/10.5194/acp-15-1161-2015, 2015.
Winiger, P., Barrett, T. E., Sheesley, R. J., Huang, L., Sharma, S., Barrie,
L. A., Yttri, K. E., Evangeliou, N., Eckhardt, S., Stohl, A., Klimont, Z.,
Heyes, C., Semiletov, I. P., Dudarev, O. V., Charkin, A., Shakhova, N., Holmstrand, H., Andersson, A., and Gustafsson, Ö.: Source apportionment of circum-Arctic atmospheric black carbon from isotopes and modeling, Sci. Adv., 5, eaau8052, https://doi.org/10.1126/sciadv.aau8052, 2019.
Yang, X., Cox, R. A., Warwick, N. J., Pyle, J. A., Carver, G. D., O'Connor, F. M., and Savage, N. H.: Tropospheric bromine chemistry and its impacts on
ozone: A model study, J. Geophys. Res.-Atmos., 110, D23311, https://doi.org/10.1029/2005jd006244, 2005.
Ye, Z., Mao, H., Lin, C. J., and Kim, S. Y.: Investigation of processes
controlling summertime gaseous elemental mercury oxidation at midlatitudinal
marine, coastal, and inland sites, Atmos. Chem. Phys., 16, 8461–8478,
https://doi.org/10.5194/acp-16-8461-2016, 2016.
Zanatta, M., Laj, P., Gysel, M., Baltensperger, U., Vratolis, S., Eleftheriadis, K., Kondo, Y., Dubuisson, P., Winiarek, V., Kazadzis, S., Tunved, P., and Jacobi, H. W.: Effects of mixing state on optical and radiative properties of black carbon in the European Arctic, Atmos. Chem.
Phys., 18, 14037–14057, https://doi.org/10.5194/acp-18-14037-2018, 2018.
Zheng, C., Wu, Y., Ting, M., Orbe, C., Wang, X., and Tilmes, S.: Summertime
Transport Pathways From Different Northern Hemisphere Regions Into the
Arctic, J. Geophys. Res.-Atmos., 126, e2020JD033811, https://doi.org/10.1029/2020JD033811, 2021.
Short summary
Atmospheric mercury species (GEM, GOM, PHg) are important constituents in the High Arctic due to their detrimental effects on human and ecosystem health. However, understanding their behavior in the High Arctic summer remains lacking. This research investigates the dynamics of mercury oxidation in the High Arctic summer. The cold, dry, sunlit free troposphere was associated with events of high GOM in the High Arctic summer, while individual events yielded unique origins.
Atmospheric mercury species (GEM, GOM, PHg) are important constituents in the High Arctic due to...
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