Articles | Volume 17, issue 4
https://doi.org/10.5194/acp-17-2689-2017
© Author(s) 2017. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Special issue:
https://doi.org/10.5194/acp-17-2689-2017
© Author(s) 2017. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Research article
| 
22 Feb 2017
Research article |
| 22 Feb 2017
Five-year records of mercury wet deposition flux at GMOS sites in the Northern and Southern hemispheres
Francesca Sprovieri
CORRESPONDING AUTHOR
CNR Institute of Atmospheric Pollution Research, Rende, Italy
Nicola Pirrone
CNR Institute of Atmospheric Pollution Research, Rome, Italy
Mariantonia Bencardino
CNR Institute of Atmospheric Pollution Research, Rende, Italy
Francesco D'Amore
CNR Institute of Atmospheric Pollution Research, Rende, Italy
Helene Angot
University Grenoble Alpes, CNRS, IRD, IGE, Grenoble, France
Carlo Barbante
University Ca' Foscari of Venice, Venice, Italy
CNR Institute for the Dynamics of Environmental Processes, Venice, Italy
Ernst-Günther Brunke
Cape Point GAW Station, Climate and Environment Research & Monitoring, South African Weather Service, Stellenbosch, South Africa
Flor Arcega-Cabrera
Universidad Nacional Autónoma de México (UNAM), Unidad de Química, Sisal, Mexico
Warren Cairns
CNR Institute for the Dynamics of Environmental Processes, Venice, Italy
Sara Comero
Joint Research Centre, Ispra, Italy
María del Carmen Diéguez
INIBIOMA-CONICET-UNComa, Bariloche, Argentina
Aurélien Dommergue
University Grenoble Alpes, CNRS, IRD, IGE, Grenoble, France
Ralf Ebinghaus
Helmholtz-Zentrum, Geesthacht, Germany
Xin Bin Feng
Institute of Geochemistry, State Key Laboratory of Environmental Geochemistry, Chinese Academy of Sciences, Guiyang, China
Institute of Geochemistry, State Key Laboratory of Environmental Geochemistry, Chinese Academy of Sciences, Guiyang, China
Patricia Elizabeth Garcia
INIBIOMA-CONICET-UNComa, Bariloche, Argentina
Bernd Manfred Gawlik
Joint Research Centre, Ispra, Italy
Ulla Hageström
IVL, Swedish Environmental Research Inst. Ltd., Göteborg, Sweden
Katarina Hansson
IVL, Swedish Environmental Research Inst. Ltd., Göteborg, Sweden
Milena Horvat
Jožef Stefan Institute, Ljubljana, Slovenia
Jože Kotnik
Jožef Stefan Institute, Ljubljana, Slovenia
Casper Labuschagne
Cape Point GAW Station, Climate and Environment Research & Monitoring, South African Weather Service, Stellenbosch, South Africa
Olivier Magand
University Grenoble Alpes, CNRS, IRD, IGE, Grenoble, France
Lynwill Martin
Cape Point GAW Station, Climate and Environment Research & Monitoring, South African Weather Service, Stellenbosch, South Africa
Nikolay Mashyanov
St. Petersburg State University, St. Petersburg, Russia
Thumeka Mkololo
Cape Point GAW Station, Climate and Environment Research & Monitoring, South African Weather Service, Stellenbosch, South Africa
John Munthe
IVL, Swedish Environmental Research Inst. Ltd., Göteborg, Sweden
Vladimir Obolkin
Limnological Institute SB RAS, Irkutsk, Russia
Martha Ramirez Islas
Instituto Nacional de Ecología y Cambio Climático (INECC), Mexico City, Mexico
Fabrizio Sena
Joint Research Centre, Ispra, Italy
Vernon Somerset
Natural Resources and the Environment (NRE), Council for Scientific and Industrial Research (CSIR), 7600 Stellenbosch, South Africa
Pia Spandow
IVL, Swedish Environmental Research Inst. Ltd., Göteborg, Sweden
Massimiliano Vardè
CNR Institute of Atmospheric Pollution Research, Rende, Italy
CNR Institute for the Dynamics of Environmental Processes, Venice, Italy
Chavon Walters
Natural Resources and the Environment (NRE), Council for Scientific and Industrial Research (CSIR), 7600 Stellenbosch, South Africa
Ingvar Wängberg
IVL, Swedish Environmental Research Inst. Ltd., Göteborg, Sweden
Andreas Weigelt
Helmholtz-Zentrum, Geesthacht, Germany
Xu Yang
Institute of Geochemistry, State Key Laboratory of Environmental Geochemistry, Chinese Academy of Sciences, Guiyang, China
Hui Zhang
Institute of Geochemistry, State Key Laboratory of Environmental Geochemistry, Chinese Academy of Sciences, Guiyang, China
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Håkan Pleijel, Jenny Klingberg, Michelle Nerentorp, Malin C. Broberg, Brigitte Nyirambangutse, John Munthe, and Göran Wallin
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Hui Zhang, Xuewu Fu, Ben Yu, Baoxin Li, Peng Liu, Guoqing Zhang, Leiming Zhang, and Xinbin Feng
Atmos. Chem. Phys., 21, 15847–15859, https://doi.org/10.5194/acp-21-15847-2021, https://doi.org/10.5194/acp-21-15847-2021, 2021
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Jan Gačnik, Igor Živković, Sergio Ribeiro Guevara, Radojko Jaćimović, Jože Kotnik, Gianmarco De Feo, Matthew A. Dexter, Warren T. Corns, and Milena Horvat
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Kai Krause, Folkard Wittrock, Andreas Richter, Stefan Schmitt, Denis Pöhler, Andreas Weigelt, and John P. Burrows
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Michele Bertò, David Cappelletti, Elena Barbaro, Cristiano Varin, Jean-Charles Gallet, Krzysztof Markowicz, Anna Rozwadowska, Mauro Mazzola, Stefano Crocchianti, Luisa Poto, Paolo Laj, Carlo Barbante, and Andrea Spolaor
Atmos. Chem. Phys., 21, 12479–12493, https://doi.org/10.5194/acp-21-12479-2021, https://doi.org/10.5194/acp-21-12479-2021, 2021
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We present the daily and seasonal variability in black carbon (BC) in surface snow inferred from two specific experiments based on the hourly and daily time resolution sampling during the Arctic spring in Svalbard. These unique data sets give us, for the first time, the opportunity to evaluate the associations between the observed surface snow BC mass concentration and a set of predictors corresponding to the considered meteorological and snow physico-chemical parameters.
Delia Segato, Maria Del Carmen Villoslada Hidalgo, Ross Edwards, Elena Barbaro, Paul Vallelonga, Helle Astrid Kjær, Marius Simonsen, Bo Vinther, Niccolò Maffezzoli, Roberta Zangrando, Clara Turetta, Dario Battistel, Orri Vésteinsson, Carlo Barbante, and Andrea Spolaor
Clim. Past, 17, 1533–1545, https://doi.org/10.5194/cp-17-1533-2021, https://doi.org/10.5194/cp-17-1533-2021, 2021
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Human influence on fire regimes in the past is poorly understood, especially at high latitudes. We present 5 kyr of fire proxies levoglucosan, black carbon, and ammonium in the RECAP ice core in Greenland and reconstruct for the first time the fire regime in the high North Atlantic region, comprising coastal east Greenland and Iceland. Climate is the main driver of the fire regime, but at 1.1 kyr BP a contribution may be made by the deforestation resulting from Viking colonization of Iceland.
Attilio Naccarato, Antonella Tassone, Maria Martino, Sacha Moretti, Antonella Macagnano, Emiliano Zampetti, Paolo Papa, Joshua Avossa, Nicola Pirrone, Michelle Nerentorp, John Munthe, Ingvar Wängberg, Geoff W. Stupple, Carl P. J. Mitchell, Adam R. Martin, Alexandra Steffen, Diana Babi, Eric M. Prestbo, Francesca Sprovieri, and Frank Wania
Atmos. Meas. Tech., 14, 3657–3672, https://doi.org/10.5194/amt-14-3657-2021, https://doi.org/10.5194/amt-14-3657-2021, 2021
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Mercury monitoring in support of the Minamata Convention requires effective and reliable analytical tools. Passive sampling is a promising approach for creating a sustainable long-term network for atmospheric mercury with improved spatial resolution and global coverage. In this study the analytical performance of three passive air samplers (CNR-PAS, IVL-PAS, and MerPAS) was assessed over extended deployment periods and the accuracy of concentrations was judged by comparison with active sampling.
Xuewu Fu, Chen Liu, Hui Zhang, Yue Xu, Hui Zhang, Jun Li, Xiaopu Lyu, Gan Zhang, Hai Guo, Xun Wang, Leiming Zhang, and Xinbin Feng
Atmos. Chem. Phys., 21, 6721–6734, https://doi.org/10.5194/acp-21-6721-2021, https://doi.org/10.5194/acp-21-6721-2021, 2021
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TGM concentrations and isotopic compositions in 10 Chinese cities showed strong seasonality with higher TGM concentrations and Δ199Hg and lower δ202Hg in summer. We found the seasonal variations in TGM concentrations and isotopic compositions were highly related to regional surface Hg(0) emissions, suggesting land surface Hg(0) emissions are an important source of atmospheric TGM that contribute dominantly to the seasonal variations in TGM concentrations and isotopic compositions.
Iris de Krom, Wijnand Bavius, Ruben Ziel, Elizabeth A. McGhee, Richard J. C. Brown, Igor Živković, Jan Gačnik, Vesna Fajon, Jože Kotnik, Milena Horvat, and Hugo Ent
Atmos. Meas. Tech., 14, 2317–2326, https://doi.org/10.5194/amt-14-2317-2021, https://doi.org/10.5194/amt-14-2317-2021, 2021
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To demonstrate the robustness and comparability of the novel primary mercury gas standard, the results of comparisons are presented with current calibration methods maintained, using the bell jar in combination with the Dumarey equation or NIST liquid standard reference material. The results show that the primary standard and the NIST reference material are comparable, whereas a difference of −8 % exists between results traceable to the primary standard and the Dumarey equation.
Alkuin Maximilian Koenig, Olivier Magand, Paolo Laj, Marcos Andrade, Isabel Moreno, Fernando Velarde, Grover Salvatierra, René Gutierrez, Luis Blacutt, Diego Aliaga, Thomas Reichler, Karine Sellegri, Olivier Laurent, Michel Ramonet, and Aurélien Dommergue
Atmos. Chem. Phys., 21, 3447–3472, https://doi.org/10.5194/acp-21-3447-2021, https://doi.org/10.5194/acp-21-3447-2021, 2021
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The environmental cycling of atmospheric mercury, a harmful global contaminant, is still not sufficiently constrained, partly due to missing data in remote regions. Here, we address this issue by presenting 20 months of atmospheric mercury measurements, sampled in the Bolivian Andes. We observe a significant seasonal pattern, whose key features we explore. Moreover, we deduce ratios to constrain South American biomass burning mercury emissions and the mercury uptake by the Amazon rainforest.
François Burgay, Andrea Spolaor, Jacopo Gabrieli, Giulio Cozzi, Clara Turetta, Paul Vallelonga, and Carlo Barbante
Clim. Past, 17, 491–505, https://doi.org/10.5194/cp-17-491-2021, https://doi.org/10.5194/cp-17-491-2021, 2021
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We present the first Fe record from the NEEM ice core, which provides insight into past atmospheric Fe deposition in the Arctic. Considering the biological relevance of Fe, we questioned if the increased eolian Fe supply during glacial periods could explain the marine productivity variability in the Fe-limited subarctic Pacific Ocean. We found no overwhelming evidence that eolian Fe fertilization triggered any phytoplankton blooms, likely because other factors play a more relevant role.
Romie Tignat-Perrier, Aurélien Dommergue, Alban Thollot, Olivier Magand, Timothy M. Vogel, and Catherine Larose
Biogeosciences, 17, 6081–6095, https://doi.org/10.5194/bg-17-6081-2020, https://doi.org/10.5194/bg-17-6081-2020, 2020
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The adverse atmospheric environmental conditions do not appear suited for microbial life. We conducted the first global comparative metagenomic analysis to find out if airborne microbial communities might be selected by their ability to resist these adverse conditions. The relatively higher concentration of fungi led to the observation of higher proportions of stress-related functions in air. Fungi might likely resist and survive atmospheric physical stress better than bacteria.
Johannes Bieser, Hélène Angot, Franz Slemr, and Lynwill Martin
Atmos. Chem. Phys., 20, 10427–10439, https://doi.org/10.5194/acp-20-10427-2020, https://doi.org/10.5194/acp-20-10427-2020, 2020
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We use numerical models to determine the origin of air masses measured for elemental gaseous mercury (GEM) at Cape Point (CPT), South Africa. Our analysis is based on 10 years of hourly GEM measurements at CPT from 2007 to 2016. Based on GEM concentration and the origin of the air mass, we identify source and sink regions at CPT. We find, that the warm Agulhas Current to the south-east is the major Hg source and the continent the major sink.
Paolo Laj, Alessandro Bigi, Clémence Rose, Elisabeth Andrews, Cathrine Lund Myhre, Martine Collaud Coen, Yong Lin, Alfred Wiedensohler, Michael Schulz, John A. Ogren, Markus Fiebig, Jonas Gliß, Augustin Mortier, Marco Pandolfi, Tuukka Petäja, Sang-Woo Kim, Wenche Aas, Jean-Philippe Putaud, Olga Mayol-Bracero, Melita Keywood, Lorenzo Labrador, Pasi Aalto, Erik Ahlberg, Lucas Alados Arboledas, Andrés Alastuey, Marcos Andrade, Begoña Artíñano, Stina Ausmeel, Todor Arsov, Eija Asmi, John Backman, Urs Baltensperger, Susanne Bastian, Olaf Bath, Johan Paul Beukes, Benjamin T. Brem, Nicolas Bukowiecki, Sébastien Conil, Cedric Couret, Derek Day, Wan Dayantolis, Anna Degorska, Konstantinos Eleftheriadis, Prodromos Fetfatzis, Olivier Favez, Harald Flentje, Maria I. Gini, Asta Gregorič, Martin Gysel-Beer, A. Gannet Hallar, Jenny Hand, Andras Hoffer, Christoph Hueglin, Rakesh K. Hooda, Antti Hyvärinen, Ivo Kalapov, Nikos Kalivitis, Anne Kasper-Giebl, Jeong Eun Kim, Giorgos Kouvarakis, Irena Kranjc, Radovan Krejci, Markku Kulmala, Casper Labuschagne, Hae-Jung Lee, Heikki Lihavainen, Neng-Huei Lin, Gunter Löschau, Krista Luoma, Angela Marinoni, Sebastiao Martins Dos Santos, Frank Meinhardt, Maik Merkel, Jean-Marc Metzger, Nikolaos Mihalopoulos, Nhat Anh Nguyen, Jakub Ondracek, Noemi Pérez, Maria Rita Perrone, Jean-Eudes Petit, David Picard, Jean-Marc Pichon, Veronique Pont, Natalia Prats, Anthony Prenni, Fabienne Reisen, Salvatore Romano, Karine Sellegri, Sangeeta Sharma, Gerhard Schauer, Patrick Sheridan, James Patrick Sherman, Maik Schütze, Andreas Schwerin, Ralf Sohmer, Mar Sorribas, Martin Steinbacher, Junying Sun, Gloria Titos, Barbara Toczko, Thomas Tuch, Pierre Tulet, Peter Tunved, Ville Vakkari, Fernando Velarde, Patricio Velasquez, Paolo Villani, Sterios Vratolis, Sheng-Hsiang Wang, Kay Weinhold, Rolf Weller, Margarita Yela, Jesus Yus-Diez, Vladimir Zdimal, Paul Zieger, and Nadezda Zikova
Atmos. Meas. Tech., 13, 4353–4392, https://doi.org/10.5194/amt-13-4353-2020, https://doi.org/10.5194/amt-13-4353-2020, 2020
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The paper establishes the fiducial reference of the GAW aerosol network providing the fully characterized value chain to the provision of four climate-relevant aerosol properties from ground-based sites. Data from almost 90 stations worldwide are reported for a reference year, 2017, providing a unique and very robust view of the variability of these variables worldwide. Current gaps in the GAW network are analysed and requirements for the Global Climate Monitoring System are proposed.
Albane Barbero, Camille Blouzon, Joël Savarino, Nicolas Caillon, Aurélien Dommergue, and Roberto Grilli
Atmos. Meas. Tech., 13, 4317–4331, https://doi.org/10.5194/amt-13-4317-2020, https://doi.org/10.5194/amt-13-4317-2020, 2020
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In this paper, we present a compact, affordable and robust instrument for in situ measurements of different trace gases: NOx, IO, CHOCHO and O3 with very low detection limits. The device weighs 15 kg and has a total electrical power consumption of < 300 W. Its very low detection limits and its design make it suitable for field applications to address different questions such as how to better constrain the oxidative capacity of the atmosphere and study the chemistry of highly reactive species.
Martine Collaud Coen, Elisabeth Andrews, Andrés Alastuey, Todor Petkov Arsov, John Backman, Benjamin T. Brem, Nicolas Bukowiecki, Cédric Couret, Konstantinos Eleftheriadis, Harald Flentje, Markus Fiebig, Martin Gysel-Beer, Jenny L. Hand, András Hoffer, Rakesh Hooda, Christoph Hueglin, Warren Joubert, Melita Keywood, Jeong Eun Kim, Sang-Woo Kim, Casper Labuschagne, Neng-Huei Lin, Yong Lin, Cathrine Lund Myhre, Krista Luoma, Hassan Lyamani, Angela Marinoni, Olga L. Mayol-Bracero, Nikos Mihalopoulos, Marco Pandolfi, Natalia Prats, Anthony J. Prenni, Jean-Philippe Putaud, Ludwig Ries, Fabienne Reisen, Karine Sellegri, Sangeeta Sharma, Patrick Sheridan, James Patrick Sherman, Junying Sun, Gloria Titos, Elvis Torres, Thomas Tuch, Rolf Weller, Alfred Wiedensohler, Paul Zieger, and Paolo Laj
Atmos. Chem. Phys., 20, 8867–8908, https://doi.org/10.5194/acp-20-8867-2020, https://doi.org/10.5194/acp-20-8867-2020, 2020
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Long-term trends of aerosol radiative properties (52 stations) prove that aerosol load has significantly decreased over the last 20 years. Scattering trends are negative in Europe (EU) and North America (NA), not ss in Asia, and show a mix of positive and negative trends at polar stations. Absorption has mainly negative trends. The single scattering albedo has positive trends in Asia and eastern EU and negative in western EU and NA, leading to a global positive median trend of 0.02 % per year.
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.
Danilo Custodio, Ralf Ebinghaus, T. Gerard Spain, and Johannes Bieser
Atmos. Chem. Phys., 20, 7929–7939, https://doi.org/10.5194/acp-20-7929-2020, https://doi.org/10.5194/acp-20-7929-2020, 2020
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Using a stereo algorithm, we reconstructed 99.9 % of the total atmospheric gas mercury and presented a new insight into atmospheric mercury source assessing, which can have great relevance for policy and regulations in light of the Minamata convention.
Michele Bertò, David Cappelletti, Elena Barbaro, Cristiano Varin, Jean-Charles Gallet, Krzysztof Markowicz, Anna Rozwadowska, Mauro Mazzola, Stefano Crocchianti, Luisa Poto, Paolo Laj, Carlo Barbante, and Andrea Spolaor
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2020-574, https://doi.org/10.5194/acp-2020-574, 2020
Preprint withdrawn
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We present the daily and seasonal variability of Black carbon inferred from two specific experiment based on the hourly and daily time resolution sampling strategy. These unique datasets give us for the first time the opportunity to evaluate the associations between the observed surface snow rBC mass concentration and a set of predictors corresponding to the considered meteorological and snow physico-chemical parameters, via a multiple linear regression approach.
Franz Slemr, Lynwill Martin, Casper Labuschagne, Thumeka Mkololo, Hélène Angot, Olivier Magand, Aurélien Dommergue, Philippe Garat, Michel Ramonet, and Johannes Bieser
Atmos. Chem. Phys., 20, 7683–7692, https://doi.org/10.5194/acp-20-7683-2020, https://doi.org/10.5194/acp-20-7683-2020, 2020
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Monitoring of atmospheric mercury (Hg) concentrations is an important part of the effectiveness evaluation of the Minamata Convention on Hg. Hg concentrations in 2012–2017 at Cape Point, South Africa, and at Amsterdam Island in the remote Indian Ocean are comparable, and no trend or a slightly downward trend was observed at both stations. Over the 2007–2017 period an upward trend was observed at CPT which was driven mainly by the 2007–2014 data. The trend and its change are discussed.
Liyuan Zhou, Åsa M. Hallquist, Mattias Hallquist, Christian M. Salvador, Samuel M. Gaita, Åke Sjödin, Martin Jerksjö, Håkan Salberg, Ingvar Wängberg, Johan Mellqvist, Qianyun Liu, Berto P. Lee, and Chak K. Chan
Atmos. Chem. Phys., 20, 1701–1722, https://doi.org/10.5194/acp-20-1701-2020, https://doi.org/10.5194/acp-20-1701-2020, 2020
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The study reports the transition in the atmospheric emission of particles and gases from on-road heavy-duty trucks (HDTs) caused by the modernisation of the fleet. We measured particle number (PN), particle mass (PM), black carbon (BC), nitrogen oxides (NOx), carbon monoxide (CO), hydrocarbon (HC), particle size distributions, and volatility in the plumes of 556 individual HDTs. Significant but different changes in emissions were evident for various pollutants with respect to emission standards.
Niccolò Maffezzoli, Paul Vallelonga, Ross Edwards, Alfonso Saiz-Lopez, Clara Turetta, Helle Astrid Kjær, Carlo Barbante, Bo Vinther, and Andrea Spolaor
Clim. Past, 15, 2031–2051, https://doi.org/10.5194/cp-15-2031-2019, https://doi.org/10.5194/cp-15-2031-2019, 2019
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This study provides the first ice-core-based history of sea ice in the North Atlantic Ocean, reaching 120 000 years back in time. This record was obtained from bromine and sodium measurements in the RECAP ice core, drilled in east Greenland. We found that, during the last deglaciation, sea ice started to melt ~ 17 500 years ago. Over the 120 000 years of the last glacial cycle, sea ice extent was maximal during MIS2, while minimum sea ice extent exists for the Holocene.
Juan Pablo Corella, Niccolo Maffezzoli, Carlos Alberto Cuevas, Paul Vallelonga, Andrea Spolaor, Giulio Cozzi, Juliane Müller, Bo Vinther, Carlo Barbante, Helle Astrid Kjær, Ross Edwards, and Alfonso Saiz-Lopez
Clim. Past, 15, 2019–2030, https://doi.org/10.5194/cp-15-2019-2019, https://doi.org/10.5194/cp-15-2019-2019, 2019
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This study provides the first reconstruction of atmospheric iodine levels in the Arctic during the last 11 700 years from an ice core record in coastal Greenland. Dramatic shifts in iodine level variability coincide with abrupt climatic transitions in the North Atlantic. Since atmospheric iodine levels have significant environmental and climatic implications, this study may serve as a past analog to predict future changes in Arctic climate in response to global warming.
Andrea Spolaor, Elena Barbaro, David Cappelletti, Clara Turetta, Mauro Mazzola, Fabio Giardi, Mats P. Björkman, Federico Lucchetta, Federico Dallo, Katrine Aspmo Pfaffhuber, Hélène Angot, Aurelien Dommergue, Marion Maturilli, Alfonso Saiz-Lopez, Carlo Barbante, and Warren R. L. Cairns
Atmos. Chem. Phys., 19, 13325–13339, https://doi.org/10.5194/acp-19-13325-2019, https://doi.org/10.5194/acp-19-13325-2019, 2019
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The main aims of the study are to (a) detect whether mercury in the surface snow undergoes a daily cycle as determined in the atmosphere, (b) compare the mercury concentration in surface snow with the concentration in the atmosphere, (c) evaluate the effect of snow depositions, (d) detect whether iodine and bromine in the surface snow undergo a daily cycle, and (e) evaluate the role of metereological and atmospheric conditions. Different behaviours were determined during different seasons.
Shaojie Song, Hélène Angot, Noelle E. Selin, Hubert Gallée, Francesca Sprovieri, Nicola Pirrone, Detlev Helmig, Joël Savarino, Olivier Magand, and Aurélien Dommergue
Atmos. Chem. Phys., 18, 15825–15840, https://doi.org/10.5194/acp-18-15825-2018, https://doi.org/10.5194/acp-18-15825-2018, 2018
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Mercury is a trace metal with adverse health effects on human and wildlife. Its unique property makes it undergo long-range transport, and even remote Antarctica receives significant inputs. This paper presents the first model that aims to understand mercury behavior over the Antarctic Plateau. We find that mercury is quickly cycled between snow and air in the sunlit period, likely driven by bromine chemistry, and that several uncertain processes contribute to its behavior in the dark period.
Alice Callegaro, Dario Battistel, Natalie M. Kehrwald, Felipe Matsubara Pereira, Torben Kirchgeorg, Maria del Carmen Villoslada Hidalgo, Broxton W. Bird, and Carlo Barbante
Clim. Past, 14, 1543–1563, https://doi.org/10.5194/cp-14-1543-2018, https://doi.org/10.5194/cp-14-1543-2018, 2018
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Holocene fires and vegetation are reconstructed using different molecular markers with a single analytical method, applied for the first time to lake sediments from Tibet. The early Holocene shows oscillations between grasses and conifers, with smouldering fires represented by levoglucosan peaks, and high-temperature fires represented by PAHs. The lack of human FeSts excludes local human influence on fire and vegetation changes. Late Holocene displays an increase in local to regional combustion.
Luca Naitza, Davide Putero, Angela Marinoni, Francescopiero Calzolari, Fabrizio Roccato, Maurizio Busetto, Damiano Sferlazzo, Eleonora Aruffo, Piero Di Carlo, Mariantonia Bencardino, Francesco D'Amore, Francesca Sprovieri, Nicola Pirrone, Federico Dallo, Jacopo Gabrieli, Massimiliano Vardè, Carlo Barbante, Paolo Bonasoni, and Paolo Cristofanelli
Atmos. Meas. Tech. Discuss., https://doi.org/10.5194/amt-2018-245, https://doi.org/10.5194/amt-2018-245, 2018
Revised manuscript not accepted
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We implemented a prototype of a centralized system to support atmospheric observatories in data production and submission. By using the “R” Language, for several near-surface ECVs, we developed specific routines for data filtering, flagging, formatting, and creation of data products for detecting instrumental problems or special atmospheric events. Our effort would improve atmospheric data quality, accelerate the process of data submission and make the data flagging more “objective".
Franz Slemr, Andreas Weigelt, Ralf Ebinghaus, Johannes Bieser, Carl A. M. Brenninkmeijer, Armin Rauthe-Schöch, Markus Hermann, Bengt G. Martinsson, Peter van Velthoven, Harald Bönisch, Marco Neumaier, Andreas Zahn, and Helmut Ziereis
Atmos. Chem. Phys., 18, 12329–12343, https://doi.org/10.5194/acp-18-12329-2018, https://doi.org/10.5194/acp-18-12329-2018, 2018
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Total and elemental mercury were measured in the upper troposphere and lower stratosphere onboard a passenger aircraft. Their concentrations in the upper troposphere were comparable implying low concentrations of oxidized mercury in this region. Large scale seasonally dependent influence of emissions from biomass burning was also observed. Their distributions in the lower stratosphere implies a long stratospheric lifetime, which precludes significant mercury oxidation by ozone.
Dario Battistel, Natalie M. Kehrwald, Piero Zennaro, Giuseppe Pellegrino, Elena Barbaro, Roberta Zangrando, Xanthi X. Pedeli, Cristiano Varin, Andrea Spolaor, Paul T. Vallelonga, Andrea Gambaro, and Carlo Barbante
Clim. Past, 14, 871–886, https://doi.org/10.5194/cp-14-871-2018, https://doi.org/10.5194/cp-14-871-2018, 2018
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From the analysis of an Antarctic ice core we showed that during the mid- to late Holocene (6000–750 BP) the long-term fire activity increased with higher rates starting at ~ 4000 BP and, more surprisingly, peaked between 2500 and 1500 BP. The anomalous increase in biomass burning centered at about 2000 BP is due to a complex interaction between changes in atmospheric circulation and biomass availability, with the main contribution coming from southern South America.
Brett Kuyper, Carl J. Palmer, Casper Labuschagne, and Chris J. C. Reason
Atmos. Chem. Phys., 18, 5785–5797, https://doi.org/10.5194/acp-18-5785-2018, https://doi.org/10.5194/acp-18-5785-2018, 2018
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Atmospheric measurements of a single biogenic compound, bromoform, released from phytoplankton and kelp were made at Cape Point, South Africa. These measurements are the first long-term, fixed-point measurements in southern Africa. This compound is the largest transport of bromine to the atmosphere, and this plays an important role in climate change. The short time series presented here shows large quantities of bromoform in the atmosphere.
Alecia Nickless, Peter J. Rayner, Francois Engelbrecht, Ernst-Günther Brunke, Birgit Erni, and Robert J. Scholes
Atmos. Chem. Phys., 18, 4765–4801, https://doi.org/10.5194/acp-18-4765-2018, https://doi.org/10.5194/acp-18-4765-2018, 2018
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Carbon dioxide emissions and uptake were estimated for Cape Town, South Africa. We placed two high-precision analysers in lighthouses located on either end of Cape Town (Robben Island and Hangklip). The Cape Point GAW station provided background measurements. We were able to improve the agreement between modelled and observed concentrations, relative to initial estimates provided. This methodology could potentially be scaled up to provide monitoring and verification of city emissions.
Lauren Schmeisser, Elisabeth Andrews, John A. Ogren, Patrick Sheridan, Anne Jefferson, Sangeeta Sharma, Jeong Eun Kim, James P. Sherman, Mar Sorribas, Ivo Kalapov, Todor Arsov, Christo Angelov, Olga L. Mayol-Bracero, Casper Labuschagne, Sang-Woo Kim, András Hoffer, Neng-Huei Lin, Hao-Ping Chia, Michael Bergin, Junying Sun, Peng Liu, and Hao Wu
Atmos. Chem. Phys., 17, 12097–12120, https://doi.org/10.5194/acp-17-12097-2017, https://doi.org/10.5194/acp-17-12097-2017, 2017
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Three methods are used to classify aerosol type from aerosol optical properties measured in situ at 24 surface sites. Classification methods work best at sites with stable, homogenous aerosol at particularly polluted and dust-prone continental and marine sites. Classification methods are poor at remote marine and Arctic sites. Using these methods to extrapolate aerosol type from optical properties can help determine aerosol radiative forcing and improve aerosol satellite retrieval algorithms.
Leiming Zhang, Seth Lyman, Huiting Mao, Che-Jen Lin, David A. Gay, Shuxiao Wang, Mae Sexauer Gustin, Xinbin Feng, and Frank Wania
Atmos. Chem. Phys., 17, 9133–9144, https://doi.org/10.5194/acp-17-9133-2017, https://doi.org/10.5194/acp-17-9133-2017, 2017
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Future research needs are proposed for improving the understanding of atmospheric mercury cycling. These include refinement of mercury emission estimations, quantification of dry deposition and air–surface exchange, improvement of the treatment of chemical mechanisms in chemical transport models, increase in the accuracy of oxidized mercury measurements, better interpretation of atmospheric mercury chemistry data, and harmonization of network operation.
Johannes Bieser, Franz Slemr, Jesse Ambrose, Carl Brenninkmeijer, Steve Brooks, Ashu Dastoor, Francesco DeSimone, Ralf Ebinghaus, Christian N. Gencarelli, Beate Geyer, Lynne E. Gratz, Ian M. Hedgecock, Daniel Jaffe, Paul Kelley, Che-Jen Lin, Lyatt Jaegle, Volker Matthias, Andrei Ryjkov, Noelle E. Selin, Shaojie Song, Oleg Travnikov, Andreas Weigelt, Winston Luke, Xinrong Ren, Andreas Zahn, Xin Yang, Yun Zhu, and Nicola Pirrone
Atmos. Chem. Phys., 17, 6925–6955, https://doi.org/10.5194/acp-17-6925-2017, https://doi.org/10.5194/acp-17-6925-2017, 2017
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We conducted a multi model study to investigate our ability to reproduce the vertical distribution of mercury in the atmosphere. For this, we used observational data from over 40 aircraft flights in EU and US. We compared observations to the results of seven chemistry transport models and found that the models are able to reproduce vertical gradients of total and elemental Hg. Finally, we found that different chemical reactions seem responsible for the oxidation of Hg depending on altitude.
Antonella Macagnano, Viviana Perri, Emiliano Zampetti, Andrea Bearzotti, Fabrizio De Cesare, Francesca Sprovieri, and Nicola Pirrone
Atmos. Chem. Phys., 17, 6883–6893, https://doi.org/10.5194/acp-17-6883-2017, https://doi.org/10.5194/acp-17-6883-2017, 2017
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By exploiting the photocatalytic properties of electrospun titania nanofibers, a novel conductometric sensor was designed and fabricated to entrap and detect GEM in air. Such a sensor was able to work at room temperature and was highly sensitive to elemental mercury. Since it is composed of titania and gold nanoparticles, it seems to be robust and resistant to common solvents and VOCs in the air.
Oleg Travnikov, Hélène Angot, Paulo Artaxo, Mariantonia Bencardino, Johannes Bieser, Francesco D'Amore, Ashu Dastoor, Francesco De Simone, María del Carmen Diéguez, Aurélien Dommergue, Ralf Ebinghaus, Xin Bin Feng, Christian N. Gencarelli, Ian M. Hedgecock, Olivier Magand, Lynwill Martin, Volker Matthias, Nikolay Mashyanov, Nicola Pirrone, Ramesh Ramachandran, Katie Alana Read, Andrei Ryjkov, Noelle E. Selin, Fabrizio Sena, Shaojie Song, Francesca Sprovieri, Dennis Wip, Ingvar Wängberg, and Xin Yang
Atmos. Chem. Phys., 17, 5271–5295, https://doi.org/10.5194/acp-17-5271-2017, https://doi.org/10.5194/acp-17-5271-2017, 2017
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The study provides a complex analysis of processes governing Hg fate in the atmosphere involving both measurement data and simulation results of chemical transport models. Evaluation of the model simulations and numerical experiments against observations allows explaining spatial and temporal variations of Hg concentration in the near-surface atmospheric layer and shows possibility of multiple pathways of Hg oxidation occurring concurrently in various parts of the atmosphere.
Niccolò Maffezzoli, Andrea Spolaor, Carlo Barbante, Michele Bertò, Massimo Frezzotti, and Paul Vallelonga
The Cryosphere, 11, 693–705, https://doi.org/10.5194/tc-11-693-2017, https://doi.org/10.5194/tc-11-693-2017, 2017
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Sea ice is a crucial parameter within Earth's climate system. Understanding its dynamics and its response to other climatic variables is therefore of primary importance in view of a warming climate and sea ice decline. In this work we investigate some features of a chemical parameter in ice cores, bromine enrichment, which is linked to sea ice and can therefore be used to reconstruct sea ice in the past.
Lynwill G. Martin, Casper Labuschagne, Ernst-Günther Brunke, Andreas Weigelt, Ralf Ebinghaus, and Franz Slemr
Atmos. Chem. Phys., 17, 2393–2399, https://doi.org/10.5194/acp-17-2393-2017, https://doi.org/10.5194/acp-17-2393-2017, 2017
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Currently the Cape Point GAW GEM record is a very sought-after data record for international modelers and scientist alike, as the data set of 20 years represents the longest record in the Southern Hemisphere (SH). CPT was the only monitoring site on the African continent and one of eight GMOS ground-based monitoring sites located in the SH. The increasing Hg trend observed at CPT is of global importance as treaties such as the Minamata Convention on Mercury is there to combat Hg pollution.
Francesco De Simone, Paulo Artaxo, Mariantonia Bencardino, Sergio Cinnirella, Francesco Carbone, Francesco D'Amore, Aurélien Dommergue, Xin Bin Feng, Christian N. Gencarelli, Ian M. Hedgecock, Matthew S. Landis, Francesca Sprovieri, Noriuki Suzuki, Ingvar Wängberg, and Nicola Pirrone
Atmos. Chem. Phys., 17, 1881–1899, https://doi.org/10.5194/acp-17-1881-2017, https://doi.org/10.5194/acp-17-1881-2017, 2017
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Biomass burning (BB) releases of Hg, usually considered to be Hg(0), are a significant global source of atmospheric Hg. However there is experimental evidence that a fraction of this Hg is bound to particulate matter, Hg(P). This modelling study shows how increasing fractions of Hg(P) reduce the availability of Hg to the global pool, raising Hg exposure for those regions characterized by high BB, with implications for the sub-Arctic and also rice-growing areas in South-East Asia.
Maria C. Diéguez, Patricia E. Garcia, Mariantonia Bencardino, Francesco D'Amore, Jessica Castagna, Sergio Ribeiro Guevara, and Francesca Sprovieri
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2016-1076, https://doi.org/10.5194/acp-2016-1076, 2017
Preprint withdrawn
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First continuous records of gaseous elemental Hg (GEM) concentrations monitored at the GMOS EMMA monitoring station in Nahuel Huapi National Park (Northwestern Patagonia, Argentina) showed seasonal and daily variation with mean values higher during spring and winter (ca. 0.92 ng m−3) and higher day-time levels across all seasons. GEM levels were determined by the westerly winds and backward trajectory analysis highlighted the influence of clean oceanic air masses and volcanoes in the Andes.
Paolo Gabrielli, Carlo Barbante, Giuliano Bertagna, Michele Bertó, Daniel Binder, Alberto Carton, Luca Carturan, Federico Cazorzi, Giulio Cozzi, Giancarlo Dalla Fontana, Mary Davis, Fabrizio De Blasi, Roberto Dinale, Gianfranco Dragà, Giuliano Dreossi, Daniela Festi, Massimo Frezzotti, Jacopo Gabrieli, Stephan P. Galos, Patrick Ginot, Petra Heidenwolf, Theo M. Jenk, Natalie Kehrwald, Donald Kenny, Olivier Magand, Volkmar Mair, Vladimir Mikhalenko, Ping Nan Lin, Klaus Oeggl, Gianni Piffer, Mirko Rinaldi, Ulrich Schotterer, Margit Schwikowski, Roberto Seppi, Andrea Spolaor, Barbara Stenni, David Tonidandel, Chiara Uglietti, Victor Zagorodnov, Thomas Zanoner, and Piero Zennaro
The Cryosphere, 10, 2779–2797, https://doi.org/10.5194/tc-10-2779-2016, https://doi.org/10.5194/tc-10-2779-2016, 2016
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New ice cores were extracted from Alto dell'Ortles, the highest glacier of South Tyrol in the Italian Alps, to check whether prehistoric ice, which is coeval to the famous 5300-yr-old Tyrolean Iceman, is still preserved in this region. Dating of the ice cores confirms the hypothesis and indicates the drilling site has been glaciated since the end of the Northern Hemisphere Climatic Optimum (7000 yrs BP). We also infer that an unprecedented acceleration of the glacier flow has recently begun.
Andreas Weigelt, Franz Slemr, Ralf Ebinghaus, Nicola Pirrone, Johannes Bieser, Jan Bödewadt, Giulio Esposito, and Peter F. J. van Velthoven
Atmos. Chem. Phys., 16, 13653–13668, https://doi.org/10.5194/acp-16-13653-2016, https://doi.org/10.5194/acp-16-13653-2016, 2016
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Hg ∕ SO2, Hg ∕ CO, and NOx ∕ SO2 emission ratios (ERs) in the plume of the coal-fired power plant (CFPP), Lippendorf, near Leipzig in Germany, were determined in August 2013. GOM fraction of mercury emissions was also assessed. Measured Hg ∕ SO2 and Hg ∕ CO ERs were consistent with the ratios calculated from annual emissions in 2013 reported by the CFPP operator. The NOx ∕ SO2 ER was somewhat lower. GOM fractions of ~ 40 % of CFPP mercury emissions in current emission inventories are overestimated.
Ingvar Wängberg, Michelle G. Nerentorp Mastromonaco, John Munthe, and Katarina Gårdfeldt
Atmos. Chem. Phys., 16, 13379–13387, https://doi.org/10.5194/acp-16-13379-2016, https://doi.org/10.5194/acp-16-13379-2016, 2016
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Within the EU-funded project, Global Mercury Observation System (GMOS) airborne mercury has been monitored at the background Råö measurement site on the western coast of Sweden from May 2012 to the end of May 2015, the following mercury species/fractions were measured: gaseous elemental mercury (GEM), particulate bound mercury (PBM) and gaseous oxidised mercury (GOM). Evidence that a significant part of the GOM measured at the Råö site has been formed in the free tropospheric air is presented.
Hui Zhang, Xuewu Fu, Che-Jen Lin, Lihai Shang, Yiping Zhang, Xinbin Feng, and Cynthia Lin
Atmos. Chem. Phys., 16, 13131–13148, https://doi.org/10.5194/acp-16-13131-2016, https://doi.org/10.5194/acp-16-13131-2016, 2016
Xuewu Fu, Wei Zhu, Hui Zhang, Jonas Sommar, Ben Yu, Xu Yang, Xun Wang, Che-Jen Lin, and Xinbin Feng
Atmos. Chem. Phys., 16, 12861–12873, https://doi.org/10.5194/acp-16-12861-2016, https://doi.org/10.5194/acp-16-12861-2016, 2016
Jozef M. Pacyna, Oleg Travnikov, Francesco De Simone, Ian M. Hedgecock, Kyrre Sundseth, Elisabeth G. Pacyna, Frits Steenhuisen, Nicola Pirrone, John Munthe, and Karin Kindbom
Atmos. Chem. Phys., 16, 12495–12511, https://doi.org/10.5194/acp-16-12495-2016, https://doi.org/10.5194/acp-16-12495-2016, 2016
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An assessment of current and future emissions, air concentrations and atmospheric deposition of mercury worldwide is presented on the basis of results obtained during the performance of the EU GMOS (Global Mercury Observation System) project. Emission estimates for mercury were prepared with the main goal of applying them in models to assess current (2013) and future (2035) air concentrations and atmospheric deposition of this contaminant.
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.
Xuewu Fu, Xu Yang, Xiaofang Lang, Jun Zhou, Hui Zhang, Ben Yu, Haiyu Yan, Che-Jen Lin, and Xinbin Feng
Atmos. Chem. Phys., 16, 11547–11562, https://doi.org/10.5194/acp-16-11547-2016, https://doi.org/10.5194/acp-16-11547-2016, 2016
Xun Wang, Che-Jen Lin, Wei Yuan, Jonas Sommar, Wei Zhu, and Xinbin Feng
Atmos. Chem. Phys., 16, 11125–11143, https://doi.org/10.5194/acp-16-11125-2016, https://doi.org/10.5194/acp-16-11125-2016, 2016
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We developed a mechanistic model for estimating the emission of elemental mercury vapor (Hg0) from natural surfaces in China. The development implements recent advancements in the understanding of air–soil and air–foliage exchange of Hg0 and redox chemistry in soil and on surfaces, incorporates the effects of soil characteristics and landuse changes by agricultural activities, and is examined through a systematic set of sensitivity simulations.
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.
Hélène Angot, Olivier Magand, Detlev Helmig, Philippe Ricaud, Boris Quennehen, Hubert Gallée, Massimo Del Guasta, Francesca Sprovieri, Nicola Pirrone, Joël Savarino, and Aurélien Dommergue
Atmos. Chem. Phys., 16, 8249–8264, https://doi.org/10.5194/acp-16-8249-2016, https://doi.org/10.5194/acp-16-8249-2016, 2016
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While the Arctic has been extensively monitored, there is still much to be learned from the Antarctic continent regarding the processes that govern the budget of atmospheric mercury species. We report here the first year-round measurements of gaseous elemental mercury (Hg(0)) in the atmosphere and in snowpack interstitial air on the East Antarctic ice sheet. The striking reactivity observed on the Antarctic plateau most likely influences the cycle of atmospheric mercury on a continental scale.
Hélène Angot, Iris Dion, Nicolas Vogel, Michel Legrand, Olivier Magand, and Aurélien Dommergue
Atmos. Chem. Phys., 16, 8265–8279, https://doi.org/10.5194/acp-16-8265-2016, https://doi.org/10.5194/acp-16-8265-2016, 2016
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This paper presents a multi-year record of atmospheric gaseous elemental mercury (Hg(0)) at Dumont d’Urville (DDU) on the East Antarctic coast. This record reveals particularities that are not seen at other coastal Antarctic sites, likely due to the more frequent arrival of inland air masses at DDU than at other coastal sites, and to the influence of oceanic air masses. This study confirms the influence of processes observed inland on the cycle of atmospheric mercury at a continental scale.
N. Pirrone, S. Cinnirella, S. Nativi, F. Sprovieri, and I. M. Hedgecock
Int. Arch. Photogramm. Remote Sens. Spatial Inf. Sci., XLI-B8, 1349–1355, https://doi.org/10.5194/isprs-archives-XLI-B8-1349-2016, https://doi.org/10.5194/isprs-archives-XLI-B8-1349-2016, 2016
Ingvar Wängberg, Ulla Hageström, Jonas Sommar, and Martin Ferm
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2016-528, https://doi.org/10.5194/acp-2016-528, 2016
Preprint withdrawn
Franz Slemr, Andreas Weigelt, Ralf Ebinghaus, Hans H. Kock, Jan Bödewadt, Carl A. M. Brenninkmeijer, Armin Rauthe-Schöch, Stefan Weber, Markus Hermann, Julia Becker, Andreas Zahn, and Bengt Martinsson
Atmos. Meas. Tech., 9, 2291–2302, https://doi.org/10.5194/amt-9-2291-2016, https://doi.org/10.5194/amt-9-2291-2016, 2016
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The goal of CARIBIC (Civil Aircraft for the Regular Investigation of the atmosphere Based on an Instrumented Container) is to carry out regular and detailed observations of atmospheric chemistry at 9–12 km altitude. Mercury has been measured since May 2005 during intercontinental flights between Europe and South and North America, Africa, and Asia. Here we describe the instrument modifications, the post-flight processing of the raw instrument signal, and the fractionation experiments.
Markus Hermann, Andreas Weigelt, Denise Assmann, Sascha Pfeifer, Thomas Müller, Thomas Conrath, Jens Voigtländer, Jost Heintzenberg, Alfred Wiedensohler, Bengt G. Martinsson, Terry Deshler, Carl A. M. Brenninkmeijer, and Andreas Zahn
Atmos. Meas. Tech., 9, 2179–2194, https://doi.org/10.5194/amt-9-2179-2016, https://doi.org/10.5194/amt-9-2179-2016, 2016
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Aerosol particles are an important component of the Earth's atmosphere. Here we describe the composition and characterization of a new optical particle size spectrometer (OPSS) for aircraft-borne measurements of the aerosol particle size distribution (how many particles there are with a certain size) in the 140–1050 nm size range. The OPSS was characterized throughout concerning its measurement capabilities (response, pressure dependence, coincidence) and validated versus balloon measurement.
Xuewu Fu, Nicolas Marusczak, Lars-Eric Heimbürger, Bastien Sauvage, François Gheusi, Eric M. Prestbo, and Jeroen E. Sonke
Atmos. Chem. Phys., 16, 5623–5639, https://doi.org/10.5194/acp-16-5623-2016, https://doi.org/10.5194/acp-16-5623-2016, 2016
Lei Zhao, Christopher W. N Anderson, Guangle Qiu, Bo Meng, Dingyong Wang, and Xinbin Feng
Biogeosciences, 13, 2429–2440, https://doi.org/10.5194/bg-13-2429-2016, https://doi.org/10.5194/bg-13-2429-2016, 2016
Wei Zhu, Che-Jen Lin, Xun Wang, Jonas Sommar, Xuewu Fu, and Xinbin Feng
Atmos. Chem. Phys., 16, 4451–4480, https://doi.org/10.5194/acp-16-4451-2016, https://doi.org/10.5194/acp-16-4451-2016, 2016
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Reliable quantification of air-surfaces flux of elemental mercury vapor (Hg0) is crucial for understanding Hg global biogeochemical cycles. In this study, we provide a comprehensive review on the state of science in the atmosphere-surface exchange of elemental Hg. We compiled an up-to-date global observational flux database and discuss the implication of flux data on global Hg budget. The knowledge gap and research needs for future measurements and modeling efforts were discussed.
Jonas Sommar, Wei Zhu, Lihai Shang, Che-Jen Lin, and Xinbin Feng
Biogeosciences, 13, 2029–2049, https://doi.org/10.5194/bg-13-2029-2016, https://doi.org/10.5194/bg-13-2029-2016, 2016
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A micrometeorological method (REA) has been implemented to assess the role of cereal crop fields in the North China Plain as a source or sink of elemental mercury vapor (Hg0) during the course of a full year. In combination with chamber measurements under the canopy, the above-canopy REA measurements provided evidence for a balance between Hg0 ground emissions and uptake of Hg0 by the crop foliage, with net emissions prevailing from the ecosystem during the majority of a year.
Andreas Weigelt, Ralf Ebinghaus, Nicola Pirrone, Johannes Bieser, Jan Bödewadt, Giulio Esposito, Franz Slemr, Peter F. J. van Velthoven, Andreas Zahn, and Helmut Ziereis
Atmos. Chem. Phys., 16, 4135–4146, https://doi.org/10.5194/acp-16-4135-2016, https://doi.org/10.5194/acp-16-4135-2016, 2016
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We show the first mercury profile measurements over Europe since 1996. Besides gaseous elemental mercury (GEM) and total gaseous mercury (TGM), the gases CO, SO2, NOx, and O3 were measured from aboard a research aircraft over four European locations. Compared to the boundary layer, the concentration of GEM and TGM in the free troposphere was 10–30% lower. Inside the individual layers no vertical gradient was apparent. Combined with CARIBIC data, a unique profile from 0.4 to 10.5 km is provided.
A. D. Venter, J. P. Beukes, P. G. van Zyl, E.-G. Brunke, C. Labuschagne, F. Slemr, R. Ebinghaus, and H. Kock
Atmos. Chem. Phys., 15, 10271–10280, https://doi.org/10.5194/acp-15-10271-2015, https://doi.org/10.5194/acp-15-10271-2015, 2015
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Statistical techniques applied to continuous high-resolution Hg data and back-trajectory analyses showed lower GEM concentrations originating from the sparsely populated semi-arid interior of SA and the marine environment, whereas higher GEM concentrations coincided with trade routes and industrial activities along the coast. Multi-linear regression indicated the relation of GEM with other atmospheric parameters. Measured and MLR data confirm a decline in GEM concentrations at CPT GAW station.
X. W. Fu, H. Zhang, B. Yu, X. Wang, C.-J. Lin, and X. B. Feng
Atmos. Chem. Phys., 15, 9455–9476, https://doi.org/10.5194/acp-15-9455-2015, https://doi.org/10.5194/acp-15-9455-2015, 2015
S. Song, N. E. Selin, A. L. Soerensen, H. Angot, R. Artz, S. Brooks, E.-G. Brunke, G. Conley, A. Dommergue, R. Ebinghaus, T. M. Holsen, D. A. Jaffe, S. Kang, P. Kelley, W. T. Luke, O. Magand, K. Marumoto, K. A. Pfaffhuber, X. Ren, G.-R. Sheu, F. Slemr, T. Warneke, A. Weigelt, P. Weiss-Penzias, D. C. Wip, and Q. Zhang
Atmos. Chem. Phys., 15, 7103–7125, https://doi.org/10.5194/acp-15-7103-2015, https://doi.org/10.5194/acp-15-7103-2015, 2015
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A better knowledge of mercury (Hg) emission fluxes into the global atmosphere is important for assessing its human health impacts and evaluating the effectiveness of corresponding policy actions. We for the first time apply a top-down approach at a global scale to quantitatively estimate present-day mercury emission sources as well as key parameters in a chemical transport model, in order to better constrain the global biogeochemical cycle of mercury.
E. J. Morgan, J. V. Lavrič, T. Seifert, T. Chicoine, A. Day, J. Gomez, R. Logan, J. Sack, T. Shuuya, E. G. Uushona, K. Vincent, U. Schultz, E.-G. Brunke, C. Labuschagne, R. L. Thompson, S. Schmidt, A. C. Manning, and M. Heimann
Atmos. Meas. Tech., 8, 2233–2250, https://doi.org/10.5194/amt-8-2233-2015, https://doi.org/10.5194/amt-8-2233-2015, 2015
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We describe the analytical techniques used in the creation of a new background site for continuous measurements of greenhouse gases, carbon monoxide, and atmospheric oxygen in the Namib Desert. The measurement system is semi-automated and optimized for operation in a remote locale. Measurement uncertainties, gas handling, calibration schemes, drift corrections, and instrument performance are discussed.
E. Barbaro, R. Zangrando, M. Vecchiato, R. Piazza, W. R. L. Cairns, G. Capodaglio, C. Barbante, and A. Gambaro
Atmos. Chem. Phys., 15, 5457–5469, https://doi.org/10.5194/acp-15-5457-2015, https://doi.org/10.5194/acp-15-5457-2015, 2015
W. Zhu, J. Sommar, C.-J. Lin, and X. Feng
Atmos. Chem. Phys., 15, 5359–5376, https://doi.org/10.5194/acp-15-5359-2015, https://doi.org/10.5194/acp-15-5359-2015, 2015
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Bias and uncertainty in Hg flux measured by micrometeorological methods (MM) and dynamic flux chambers (DFCs) are assessed from two field inter-comparison campaigns.
DFC flux bias follows a diurnal cycle due to modified temperature and radiation balance inside the chamber.
The precision in concentration difference measurements poses critical constraint on obtaining a larger fraction of significant MM flux. Asynchronous sampling impairs flux accuracy under varying atmospheric Hg concentration.
F. Slemr, H. Angot, A. Dommergue, O. Magand, M. Barret, A. Weigelt, R. Ebinghaus, E.-G. Brunke, K. A. Pfaffhuber, G. Edwards, D. Howard, J. Powell, M. Keywood, and F. Wang
Atmos. Chem. Phys., 15, 3125–3133, https://doi.org/10.5194/acp-15-3125-2015, https://doi.org/10.5194/acp-15-3125-2015, 2015
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• Longer-term mercury measurement in the Southern Hemisphere is compared.
• Mercury, in terms of monthly and annual medians and averages, is more evenly distributed than hitherto believed.
• Consequently, trends observed at one or a few sites are likely to be representative of the whole hemisphere, and smaller trends can be detected in shorter time periods.
• We report a change in the trend sign at Cape Point from decreasing mercury concentrations in 1996-2004 to increasing ones since 2007.
X. W. Fu, H. Zhang, C.-J. Lin, X. B. Feng, L. X. Zhou, and S. X. Fang
Atmos. Chem. Phys., 15, 1013–1028, https://doi.org/10.5194/acp-15-1013-2015, https://doi.org/10.5194/acp-15-1013-2015, 2015
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This paper is the first to report correlation slopes of GEM/CO, GEM/CO2, GEM/CH4, CH4/CO, CH4/CO2, and CO/CO2 for mainland China, South Asia, the Indochinese Peninsula, and Central Asia, and applied the values to estimate GEM emissions in the four source regions. The estimated Hg0 emissions for mainland China, South Asia, the Indochinese Peninsula, and Central Asia using GEM/CO and GEM/CO2 correlation slopes are in the ranges of 1071-1187, 340-470, 125, and 54-90t, respectively.
H. Zhang, X. W. Fu, C.-J. Lin, X. Wang, and X. B. Feng
Atmos. Chem. Phys., 15, 653–665, https://doi.org/10.5194/acp-15-653-2015, https://doi.org/10.5194/acp-15-653-2015, 2015
W. Zhu, J. Sommar, C.-J. Lin, and X. Feng
Atmos. Chem. Phys., 15, 685–702, https://doi.org/10.5194/acp-15-685-2015, https://doi.org/10.5194/acp-15-685-2015, 2015
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Mercury vapor fluxes measured by the micrometeorological (MM) and dynamic flux chambers (DFCs) methods were compared. Distinct temporal trends existed between MM and DFCs fluxes; the novel chamber method provided net cumulative flux on a level with those derived by MM methods. Statistical analysis indicated that the medians of turbulent fluxes estimated by three MM techniques were not significantly different. Recommendations are given regarding the deployment of Hg flux quantification methods.
P. Zennaro, N. Kehrwald, J. R. McConnell, S. Schüpbach, O. J. Maselli, J. Marlon, P. Vallelonga, D. Leuenberger, R. Zangrando, A. Spolaor, M. Borrotti, E. Barbaro, A. Gambaro, and C. Barbante
Clim. Past, 10, 1905–1924, https://doi.org/10.5194/cp-10-1905-2014, https://doi.org/10.5194/cp-10-1905-2014, 2014
A. Spolaor, P. Vallelonga, J. Gabrieli, T. Martma, M. P. Björkman, E. Isaksson, G. Cozzi, C. Turetta, H. A. Kjær, M. A. J. Curran, A. D. Moy, A. Schönhardt, A.-M. Blechschmidt, J. P. Burrows, J. M. C. Plane, and C. Barbante
Atmos. Chem. Phys., 14, 9613–9622, https://doi.org/10.5194/acp-14-9613-2014, https://doi.org/10.5194/acp-14-9613-2014, 2014
M. D. Mulder, A. Heil, P. Kukučka, J. Klánová, J. Kuta, R. Prokeš, F. Sprovieri, and G. Lammel
Atmos. Chem. Phys., 14, 8905–8915, https://doi.org/10.5194/acp-14-8905-2014, https://doi.org/10.5194/acp-14-8905-2014, 2014
E. Barbaro, R. Zangrando, M. Vecchiato, R. Piazza, G. Capodaglio, C. Barbante, and A. Gambaro
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acpd-14-17067-2014, https://doi.org/10.5194/acpd-14-17067-2014, 2014
Revised manuscript not accepted
X. Wang, C.-J. Lin, and X. Feng
Atmos. Chem. Phys., 14, 6273–6287, https://doi.org/10.5194/acp-14-6273-2014, https://doi.org/10.5194/acp-14-6273-2014, 2014
H. F. Zhang, B. Z. Chen, I. T. van der Laan-Luijk, T. Machida, H. Matsueda, Y. Sawa, Y. Fukuyama, R. Langenfelds, M. van der Schoot, G. Xu, J. W. Yan, M. L. Cheng, L. X. Zhou, P. P. Tans, and W. Peters
Atmos. Chem. Phys., 14, 5807–5824, https://doi.org/10.5194/acp-14-5807-2014, https://doi.org/10.5194/acp-14-5807-2014, 2014
S. Schüpbach, U. Federer, P. R. Kaufmann, S. Albani, C. Barbante, T. F. Stocker, and H. Fischer
Clim. Past, 9, 2789–2807, https://doi.org/10.5194/cp-9-2789-2013, https://doi.org/10.5194/cp-9-2789-2013, 2013
A. Spolaor, J. Gabrieli, T. Martma, J. Kohler, M. B. Björkman, E. Isaksson, C. Varin, P. Vallelonga, J. M. C. Plane, and C. Barbante
The Cryosphere, 7, 1645–1658, https://doi.org/10.5194/tc-7-1645-2013, https://doi.org/10.5194/tc-7-1645-2013, 2013
A. Spolaor, P. Vallelonga, J. M. C. Plane, N. Kehrwald, J. Gabrieli, C. Varin, C. Turetta, G. Cozzi, R. Kumar, C. Boutron, and C. Barbante
Atmos. Chem. Phys., 13, 6623–6635, https://doi.org/10.5194/acp-13-6623-2013, https://doi.org/10.5194/acp-13-6623-2013, 2013
F. Slemr, E.-G. Brunke, S. Whittlestone, W. Zahorowski, R. Ebinghaus, H. H. Kock, and C. Labuschagne
Atmos. Chem. Phys., 13, 6421–6428, https://doi.org/10.5194/acp-13-6421-2013, https://doi.org/10.5194/acp-13-6421-2013, 2013
C. Barbante, N. M. Kehrwald, P. Marianelli, B. M. Vinther, J. P. Steffensen, G. Cozzi, C. U. Hammer, H. B. Clausen, and M.-L. Siggaard-Andersen
Clim. Past, 9, 1221–1232, https://doi.org/10.5194/cp-9-1221-2013, https://doi.org/10.5194/cp-9-1221-2013, 2013
P. Vallelonga, C. Barbante, G. Cozzi, J. Gabrieli, S. Schüpbach, A. Spolaor, and C. Turetta
Clim. Past, 9, 597–604, https://doi.org/10.5194/cp-9-597-2013, https://doi.org/10.5194/cp-9-597-2013, 2013
Related subject area
Subject: Clouds and Precipitation | Research Activity: Field Measurements | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Influences of sources and weather dynamics on atmospheric deposition of Se species and other trace elements
Response patterns of moss to atmospheric nitrogen deposition and nitrogen saturation in an urban-agro-forest transition
Molecular composition of clouds: a comparison between samples collected at tropical (Réunion Island, France) and mid-north (puy de Dôme, France) latitudes
Revealing the chemical characteristics of Arctic low-level cloud residuals – in situ observations from a mountain site
Long-term monitoring of cloud water chemistry at Whiteface Mountain: the emergence of a new chemical regime
Measurement report: Closure analysis of aerosol–cloud composition in tropical maritime warm convection
Free amino acid quantification in cloud water at the Puy de Dôme station (France)
Wet deposition in the remote western and central Mediterranean as a source of trace metals to surface seawater
Insights into tropical cloud chemistry in Réunion (Indian Ocean): results from the BIO-MAÏDO campaign
Measurement report: Molecular characteristics of cloud water in southern China and insights into aqueous-phase processes from Fourier transform ion cyclotron resonance mass spectrometry
Total organic carbon and the contribution from speciated organics in cloud water: airborne data analysis from the CAMP2Ex field campaign
A link between the ice nucleation activity and the biogeochemistry of seawater
Impact of convection on the upper-tropospheric composition (water vapor and ozone) over a subtropical site (Réunion island; 21.1° S, 55.5° E) in the Indian Ocean
Chemical characteristics of cloud water and the impacts on aerosol properties at a subtropical mountain site in Hong Kong SAR
Diurnal cycle of iodine, bromine, and mercury concentrations in Svalbard surface snow
Wet deposition of inorganic ions in 320 cities across China: spatio-temporal variation, source apportionment, and dominant factors
Deposition of ionic species and black carbon to the Arctic snowpack: combining snow pit observations with modeling
Mercury and trace metal wet deposition across five stations in Alaska: controlling factors, spatial patterns, and source regions
Drivers of atmospheric deposition of polycyclic aromatic hydrocarbons at European high-altitude sites
Cloud scavenging of anthropogenic refractory particles at a mountain site in North China
Composition of ice particle residuals in mixed-phase clouds at Jungfraujoch (Switzerland): enrichment and depletion of particle groups relative to total aerosol
Snow scavenging and phase partitioning of nitrated and oxygenated aromatic hydrocarbons in polluted and remote environments in central Europe and the European Arctic
Continuous non-marine inputs of per- and polyfluoroalkyl substances to the High Arctic: a multi-decadal temporal record
Biogenic, urban, and wildfire influences on the molecular composition of dissolved organic compounds in cloud water
The single-particle mixing state and cloud scavenging of black carbon: a case study at a high-altitude mountain site in southern China
Composition, size and cloud condensation nuclei activity of biomass burning aerosol from northern Australian savannah fires
Atmospheric wet and litterfall mercury deposition at urban and rural sites in China
Hydroxyl radical in/on illuminated polar snow: formation rates, lifetimes, and steady-state concentrations
Cloud water composition during HCCT-2010: Scavenging efficiencies, solute concentrations, and droplet size dependence of inorganic ions and dissolved organic carbon
Fog composition at Baengnyeong Island in the eastern Yellow Sea: detecting markers of aqueous atmospheric oxidations
Wet deposition of atmospheric inorganic nitrogen at five remote sites in the Tibetan Plateau
Atmospheric wet and dry deposition of trace elements at 10 sites in Northern China
Natural or anthropogenic? On the origin of atmospheric sulfate deposition in the Andes of southeastern Ecuador
Temporal variations in rainwater methanol
Comprehensive assessment of meteorological conditions and airflow connectivity during HCCT-2010
Influence of cloud processing on CCN activation behaviour in the Thuringian Forest, Germany during HCCT-2010
Classification of clouds sampled at the puy de Dôme (France) based on 10 yr of monitoring of their physicochemical properties
Preliminary signs of the initiation of deep convection by GNSS
Dissolved organic carbon (DOC) and select aldehydes in cloud and fog water: the role of the aqueous phase in impacting trace gas budgets
Insights into dissolved organic matter complexity in rainwater from continental and coastal storms by ultrahigh resolution Fourier transform ion cyclotron resonance mass spectrometry
Dynamics of the chemical composition of rainwater throughout Hurricane Irene
Spatial and temporal distributions of total and methyl mercury in precipitation in core urban areas, Chongqing, China
Wet and dry deposition of atmospheric nitrogen at ten sites in Northern China
Spatial distribution of mercury deposition fluxes in Wanshan Hg mining area, Guizhou province, China
Molecular characterization of water soluble organic nitrogen in marine rainwater by ultra-high resolution electrospray ionization mass spectrometry
Five-year record of atmospheric precipitation chemistry in urban Beijing, China
Mercury deposition in Southern New Hampshire, 2006–2009
Chemical composition of rainwater at Maldives Climate Observatory at Hanimaadhoo (MCOH)
Chemistry of rain events in West Africa: evidence of dust and biogenic influence in convective systems
Atmospheric deposition of mercury and major ions to the Pensacola (Florida) watershed: spatial, seasonal, and inter-annual variability
Esther S. Breuninger, Julie Tolu, Iris Thurnherr, Franziska Aemisegger, Aryeh Feinberg, Sylvain Bouchet, Jeroen E. Sonke, Véronique Pont, Heini Wernli, and Lenny H. E. Winkel
Atmos. Chem. Phys., 24, 2491–2510, https://doi.org/10.5194/acp-24-2491-2024, https://doi.org/10.5194/acp-24-2491-2024, 2024
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Atmospheric deposition is an important source of selenium (Se) and other health-relevant trace elements in surface environments. We found that the variability in elemental concentrations in atmospheric deposition reflects not only changes in emission sources but also weather conditions during atmospheric removal. Depending on the sources and if Se is derived more locally or from further away, the Se forms can be different, affecting the bioavailability of Se atmospherically supplied to soils.
Ouping Deng, Yuanyuan Chen, Jingze Zhao, Xi Li, Wei Zhou, Ting Lan, Dinghua Ou, Yanyan Zhang, Jiang Liu, Ling Luo, Yueqiang He, Hanqing Yang, and Rong Huang
EGUsphere, https://doi.org/10.5194/egusphere-2023-2718, https://doi.org/10.5194/egusphere-2023-2718, 2023
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Estimating atmospheric nitrogen (N) deposition is critical to understanding the biogeochemical N cycle. Moss has long been considered as a bio-indicator for N deposition due to their accumulation of N from the atmosphere. Here, we improved the method for atmospheric N deposition monitoring using mosses. The sampling frequency and time was optimized. Eventually, this study contributed to improve the accuracy of the model of quantifying N deposition by using mosses.
Lucas Pailler, Laurent Deguillaume, Hélène Lavanant, Isabelle Schmitz, Marie Hubert, Edith Nicol, Micakël Ribeiro, Jean-Marc Pichon, Mickaël Vaïtilingom, Pamela Dominutti, Frédéric Burnet, Pierre Tulet, Maud Leriche, and Angelica Bianco
EGUsphere, https://doi.org/10.5194/egusphere-2023-2706, https://doi.org/10.5194/egusphere-2023-2706, 2023
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The composition of cloud water dissolved organic matter has been investigated through non-targeted high resolution mass spectrometry only on few samples, collected in the Northern hemisphere (NH). In this work, the chemical composition of samples collected at Reunion Island (SH) is investigated and compared to samples collected at the puy de Dôme (NH). Sampling, analysis and data treatment with the same methodology produced a unique dataset for investigating the molecular composition of clouds.
Yvette Gramlich, Karolina Siegel, Sophie L. Haslett, Gabriel Freitas, Radovan Krejci, Paul Zieger, and Claudia Mohr
Atmos. Chem. Phys., 23, 6813–6834, https://doi.org/10.5194/acp-23-6813-2023, https://doi.org/10.5194/acp-23-6813-2023, 2023
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In this study, we investigate the chemical composition of aerosol particles forming clouds in the Arctic. During year-long observations at a mountain site on Svalbard, we find a large contribution of naturally derived aerosol particles in the fraction forming clouds in the summer. Our observations indicate that most aerosol particles can serve as cloud seeds in this remote environment.
Christopher E. Lawrence, Paul Casson, Richard Brandt, James J. Schwab, James E. Dukett, Phil Snyder, Elizabeth Yerger, Daniel Kelting, Trevor C. VandenBoer, and Sara Lance
Atmos. Chem. Phys., 23, 1619–1639, https://doi.org/10.5194/acp-23-1619-2023, https://doi.org/10.5194/acp-23-1619-2023, 2023
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Atmospheric aqueous chemistry can have profound effects on our environment, as illustrated by historical data from Whiteface Mountain (WFM) that were critical for uncovering the process of acid rain. The current study updates the long-term trends in cloud water composition at WFM for the period 1994 to 2021. We highlight the emergence of a new chemical regime at WFM dominated by organics and ammonium, quite different from the highly acidic regime observed in the past but not necessarily
clean.
Ewan Crosbie, Luke D. Ziemba, Michael A. Shook, Claire E. Robinson, Edward L. Winstead, K. Lee Thornhill, Rachel A. Braun, Alexander B. MacDonald, Connor Stahl, Armin Sorooshian, Susan C. van den Heever, Joshua P. DiGangi, Glenn S. Diskin, Sarah Woods, Paola Bañaga, Matthew D. Brown, Francesca Gallo, Miguel Ricardo A. Hilario, Carolyn E. Jordan, Gabrielle R. Leung, Richard H. Moore, Kevin J. Sanchez, Taylor J. Shingler, and Elizabeth B. Wiggins
Atmos. Chem. Phys., 22, 13269–13302, https://doi.org/10.5194/acp-22-13269-2022, https://doi.org/10.5194/acp-22-13269-2022, 2022
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The linkage between cloud droplet and aerosol particle chemical composition was analyzed using samples collected in a polluted tropical marine environment. Variations in the droplet composition were related to physical and dynamical processes in clouds to assess their relative significance across three cases that spanned a range of rainfall amounts. In spite of the pollution, sea salt still remained a major contributor to the droplet composition and was preferentially enhanced in rainwater.
Pascal Renard, Maxence Brissy, Florent Rossi, Martin Leremboure, Saly Jaber, Jean-Luc Baray, Angelica Bianco, Anne-Marie Delort, and Laurent Deguillaume
Atmos. Chem. Phys., 22, 2467–2486, https://doi.org/10.5194/acp-22-2467-2022, https://doi.org/10.5194/acp-22-2467-2022, 2022
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Amino acids (AAs) have been quantified in cloud water collected at the Puy de Dôme station (France). Concentrations and speciation of those compounds are highly variable among the samples. Sources from the sea surface and atmospheric transformations during the air mass transport, mainly in the free troposphere, have been shown to modulate AA levels in cloud water.
Karine Desboeufs, Franck Fu, Matthieu Bressac, Antonio Tovar-Sánchez, Sylvain Triquet, Jean-François Doussin, Chiara Giorio, Patrick Chazette, Julie Disnaquet, Anaïs Feron, Paola Formenti, Franck Maisonneuve, Araceli Rodríguez-Romero, Pascal Zapf, François Dulac, and Cécile Guieu
Atmos. Chem. Phys., 22, 2309–2332, https://doi.org/10.5194/acp-22-2309-2022, https://doi.org/10.5194/acp-22-2309-2022, 2022
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This article reports the first concurrent sampling of wet deposition samples and surface seawater and was performed during the PEACETIME cruise in the remote Mediterranean (May–June 2017). Through the chemical composition of trace metals (TMs) in these samples, it emphasizes the decrease of atmospheric metal pollution in this area during the last few decades and the critical role of wet deposition as source of TMs for Mediterranean surface seawater, especially for intense dust deposition events.
Pamela A. Dominutti, Pascal Renard, Mickaël Vaïtilingom, Angelica Bianco, Jean-Luc Baray, Agnès Borbon, Thierry Bourianne, Frédéric Burnet, Aurélie Colomb, Anne-Marie Delort, Valentin Duflot, Stephan Houdier, Jean-Luc Jaffrezo, Muriel Joly, Martin Leremboure, Jean-Marc Metzger, Jean-Marc Pichon, Mickaël Ribeiro, Manon Rocco, Pierre Tulet, Anthony Vella, Maud Leriche, and Laurent Deguillaume
Atmos. Chem. Phys., 22, 505–533, https://doi.org/10.5194/acp-22-505-2022, https://doi.org/10.5194/acp-22-505-2022, 2022
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We present here the results obtained during an intensive field campaign conducted in March to April 2019 in Reunion. Our study integrates a comprehensive chemical and microphysical characterization of cloud water. Our investigations reveal that air mass history and cloud microphysical properties do not fully explain the variability observed in their chemical composition. This highlights the complexity of emission sources, multiphasic exchanges, and transformations in clouds.
Wei Sun, Yuzhen Fu, Guohua Zhang, Yuxiang Yang, Feng Jiang, Xiufeng Lian, Bin Jiang, Yuhong Liao, Xinhui Bi, Duohong Chen, Jianmin Chen, Xinming Wang, Jie Ou, Ping'an Peng, and Guoying Sheng
Atmos. Chem. Phys., 21, 16631–16644, https://doi.org/10.5194/acp-21-16631-2021, https://doi.org/10.5194/acp-21-16631-2021, 2021
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We sampled cloud water at a remote mountain site and investigated the molecular characteristics. CHON and CHO are dominant in cloud water. No statistical difference in the oxidation state is observed between cloud water and interstitial PM2.5. Most of the formulas are aliphatic and olefinic species. CHON, with aromatic structures and organosulfates, are abundant, especially in nighttime samples. The in-cloud and multi-phase dark reactions likely contribute significantly.
Connor Stahl, Ewan Crosbie, Paola Angela Bañaga, Grace Betito, Rachel A. Braun, Zenn Marie Cainglet, Maria Obiminda Cambaliza, Melliza Templonuevo Cruz, Julie Mae Dado, Miguel Ricardo A. Hilario, Gabrielle Frances Leung, Alexander B. MacDonald, Angela Monina Magnaye, Jeffrey Reid, Claire Robinson, Michael A. Shook, James Bernard Simpas, Shane Marie Visaga, Edward Winstead, Luke Ziemba, and Armin Sorooshian
Atmos. Chem. Phys., 21, 14109–14129, https://doi.org/10.5194/acp-21-14109-2021, https://doi.org/10.5194/acp-21-14109-2021, 2021
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A total of 159 cloud water samples were collected and measured for total organic carbon (TOC) during CAMP2Ex. On average, 30 % of TOC was speciated based on carboxylic/sulfonic acids and dimethylamine. Results provide a critical constraint on cloud composition and vertical profiles of TOC and organic species ranging from ~250 m to ~ 7 km and representing a variety of cloud types and air mass source influences such as biomass burning, marine emissions, anthropogenic activity, and dust.
Martin J. Wolf, Megan Goodell, Eric Dong, Lilian A. Dove, Cuiqi Zhang, Lesly J. Franco, Chuanyang Shen, Emma G. Rutkowski, Domenic N. Narducci, Susan Mullen, Andrew R. Babbin, and Daniel J. Cziczo
Atmos. Chem. Phys., 20, 15341–15356, https://doi.org/10.5194/acp-20-15341-2020, https://doi.org/10.5194/acp-20-15341-2020, 2020
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Sea spray is the largest aerosol source on Earth. These aerosol particles can impact climate by inducing ice formation in clouds. The role that ocean biology plays in determining the composition and ice nucleation abilities of sea spray aerosol is unclarified. In this study, we demonstrate that atomized seawater from highly productive ocean regions is more effective at nucleating ice than seawater from lower-productivity regions.
Damien Héron, Stéphanie Evan, Jérôme Brioude, Karen Rosenlof, Françoise Posny, Jean-Marc Metzger, and Jean-Pierre Cammas
Atmos. Chem. Phys., 20, 8611–8626, https://doi.org/10.5194/acp-20-8611-2020, https://doi.org/10.5194/acp-20-8611-2020, 2020
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Using a statistical method, summer variations (between 2013 and 2016) of ozone and water vapor are characterized in the upper troposphere above Réunion island (21° S, 55° E). It suggests a convective influence between 9 and 13 km. As deep convection is rarely observed near Réunion island, this study provides new insights on the long-range impact of deep convective outflow from the Intertropical Convergence Zone (ITCZ) on the upper troposphere over a subtropical site.
Tao Li, Zhe Wang, Yaru Wang, Chen Wu, Yiheng Liang, Men Xia, Chuan Yu, Hui Yun, Weihao Wang, Yan Wang, Jia Guo, Hartmut Herrmann, and Tao Wang
Atmos. Chem. Phys., 20, 391–407, https://doi.org/10.5194/acp-20-391-2020, https://doi.org/10.5194/acp-20-391-2020, 2020
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This work presents a field study of cloud water chemistry and interactions of cloud, gas, and aerosols in the polluted coastal boundary layer in southern China. Substantial dissolved organic matter in the acidic cloud water was observed, and the gas- and aqueous-phase partitioning of carbonyl compounds was investigated. The results demonstrated the significant role of cloud processing in altering aerosol properties, especially in producing aqueous organics and droplet-mode aerosols.
Andrea Spolaor, Elena Barbaro, David Cappelletti, Clara Turetta, Mauro Mazzola, Fabio Giardi, Mats P. Björkman, Federico Lucchetta, Federico Dallo, Katrine Aspmo Pfaffhuber, Hélène Angot, Aurelien Dommergue, Marion Maturilli, Alfonso Saiz-Lopez, Carlo Barbante, and Warren R. L. Cairns
Atmos. Chem. Phys., 19, 13325–13339, https://doi.org/10.5194/acp-19-13325-2019, https://doi.org/10.5194/acp-19-13325-2019, 2019
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The main aims of the study are to (a) detect whether mercury in the surface snow undergoes a daily cycle as determined in the atmosphere, (b) compare the mercury concentration in surface snow with the concentration in the atmosphere, (c) evaluate the effect of snow depositions, (d) detect whether iodine and bromine in the surface snow undergo a daily cycle, and (e) evaluate the role of metereological and atmospheric conditions. Different behaviours were determined during different seasons.
Rui Li, Lulu Cui, Yilong Zhao, Ziyu Zhang, Tianming Sun, Junlin Li, Wenhui Zhou, Ya Meng, Kan Huang, and Hongbo Fu
Atmos. Chem. Phys., 19, 11043–11070, https://doi.org/10.5194/acp-19-11043-2019, https://doi.org/10.5194/acp-19-11043-2019, 2019
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Acid deposition is still an important environmental issue in China. Rainwater samples in 320 cities in China were collected to determine the acidic ion concentrations and identify their spatiotemporal variations and sources. The higher acidic ions showed higher concentrations in winter. Furthermore, the highest acidic ion concentrations were mainly distributed in YRD and SB. These acidic ions were mainly sourced from industrial emissions and agricultural activities.
Hans-Werner Jacobi, Friedrich Obleitner, Sophie Da Costa, Patrick Ginot, Konstantinos Eleftheriadis, Wenche Aas, and Marco Zanatta
Atmos. Chem. Phys., 19, 10361–10377, https://doi.org/10.5194/acp-19-10361-2019, https://doi.org/10.5194/acp-19-10361-2019, 2019
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By combining atmospheric, precipitation, and snow measurements with snowpack simulations for a high Arctic site in Svalbard, we find that during wintertime the transfer of sea salt components to the snowpack was largely dominated by wet deposition. However, dry deposition contributed significantly for nitrate, non-sea-salt sulfate, and black carbon. The comparison of monthly deposition and snow budgets indicates an important redistribution of the impurities in the snowpack even during winter.
Christopher Pearson, Dean Howard, Christopher Moore, and Daniel Obrist
Atmos. Chem. Phys., 19, 6913–6929, https://doi.org/10.5194/acp-19-6913-2019, https://doi.org/10.5194/acp-19-6913-2019, 2019
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Precipitation-based deposition of mercury and other trace metals throughout Alaska provides a significant input of pollutants. Deposition shows significant seasonal and spatial variability, largely driven by precipitation patterns. Annual wet deposition of Hg at all AK collection sites is consistently lower than other monitoring stations throughout the CONUS. Hg showed no clear relationship to other metals, likely due to its highly volatile nature and capability of long-range transport.
Lourdes Arellano, Pilar Fernández, Barend L. van Drooge, Neil L. Rose, Ulrike Nickus, Hansjoerg Thies, Evzen Stuchlík, Lluís Camarero, Jordi Catalan, and Joan O. Grimalt
Atmos. Chem. Phys., 18, 16081–16097, https://doi.org/10.5194/acp-18-16081-2018, https://doi.org/10.5194/acp-18-16081-2018, 2018
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Mountain areas are key for studying the impact of diffuse pollution due to human activities on the continental areas. Polycyclic aromatic hydrocarbons (PAHs), human carcinogens with increased levels since the 1950s, are significant constituents of this pollution. We determined PAHs in monthly atmospheric deposition collected in European high mountain areas. The number of sites, period of study and sampling frequency provide the most comprehensive description of PAH fallout at remote sites.
Lei Liu, Jian Zhang, Liang Xu, Qi Yuan, Dao Huang, Jianmin Chen, Zongbo Shi, Yele Sun, Pingqing Fu, Zifa Wang, Daizhou Zhang, and Weijun Li
Atmos. Chem. Phys., 18, 14681–14693, https://doi.org/10.5194/acp-18-14681-2018, https://doi.org/10.5194/acp-18-14681-2018, 2018
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Using transmission electron microscopy, we studied individual cloud droplet residual and interstitial particles collected in cloud events at Mt. Tai in the polluted North China region. We found that individual cloud droplets were an extremely complicated mixture containing abundant refractory soot (i.e., black carbon), fly ash, and metals. The complicated cloud droplets have not been reported in clean continental or marine air before.
Stine Eriksen Hammer, Stephan Mertes, Johannes Schneider, Martin Ebert, Konrad Kandler, and Stephan Weinbruch
Atmos. Chem. Phys., 18, 13987–14003, https://doi.org/10.5194/acp-18-13987-2018, https://doi.org/10.5194/acp-18-13987-2018, 2018
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It is important to study ice-nucleating particles in the environment to learn more about cloud formation. We studied the composition of ice particle residuals and total aerosol particles sampled in parallel during mixed-phase cloud events at Jungfraujoch and discovered that soot and complex secondary particles were not present. In contrast, silica, aluminosilicates, and other aluminosilicates were the most important ice particle residual groups at site temperatures between −11 and −18 °C.
Pourya Shahpoury, Zoran Kitanovski, and Gerhard Lammel
Atmos. Chem. Phys., 18, 13495–13510, https://doi.org/10.5194/acp-18-13495-2018, https://doi.org/10.5194/acp-18-13495-2018, 2018
Heidi M. Pickard, Alison S. Criscitiello, Christine Spencer, Martin J. Sharp, Derek C. G. Muir, Amila O. De Silva, and Cora J. Young
Atmos. Chem. Phys., 18, 5045–5058, https://doi.org/10.5194/acp-18-5045-2018, https://doi.org/10.5194/acp-18-5045-2018, 2018
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Perfluoroalkyl acids (PFAAs) are persistent, bioaccumulative compounds found in the environment far from source regions, including the remote Arctic. We collected a 15 m ice core from the Canadian High Arctic to measure a 38-year deposition record of PFAAs, proving information about major pollutant sources and production changes over time. Our results demonstrate that PFAAs have continuous and increasing deposition, despite recent North American regulations and phase-outs.
Ryan D. Cook, Ying-Hsuan Lin, Zhuoyu Peng, Eric Boone, Rosalie K. Chu, James E. Dukett, Matthew J. Gunsch, Wuliang Zhang, Nikola Tolic, Alexander Laskin, and Kerri A. Pratt
Atmos. Chem. Phys., 17, 15167–15180, https://doi.org/10.5194/acp-17-15167-2017, https://doi.org/10.5194/acp-17-15167-2017, 2017
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Reactions occur within water in both atmospheric particles and cloud droplets, yet little is known about the organic compounds in cloud water. In this work, cloud water samples were collected at Whiteface Mountain, New York, and analyzed using ultra-high-resolution mass spectrometry to investigate the molecular composition of the dissolved organic compounds. The results focus on changes in cloud water composition with air mass origin – influences of forest, urban, and wildfire emissions.
Guohua Zhang, Qinhao Lin, Long Peng, Xinhui Bi, Duohong Chen, Mei Li, Lei Li, Fred J. Brechtel, Jianxin Chen, Weijun Yan, Xinming Wang, Ping'an Peng, Guoying Sheng, and Zhen Zhou
Atmos. Chem. Phys., 17, 14975–14985, https://doi.org/10.5194/acp-17-14975-2017, https://doi.org/10.5194/acp-17-14975-2017, 2017
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The mixing state of black carbon (BC)-containing particles and the mass scavenging efficiency of BC in cloud were investigated at a mountain site (1690 m a.s.l.) in southern China. The measured BC-containing particles were internally mixed extensively with sulfate, and thus the number fraction of scavenged BC-containing particles is close to that of all the measured particles. BC-containing particles with higher fractions of organics were scavenged relatively less.
Marc D. Mallet, Luke T. Cravigan, Andelija Milic, Joel Alroe, Zoran D. Ristovski, Jason Ward, Melita Keywood, Leah R. Williams, Paul Selleck, and Branka Miljevic
Atmos. Chem. Phys., 17, 3605–3617, https://doi.org/10.5194/acp-17-3605-2017, https://doi.org/10.5194/acp-17-3605-2017, 2017
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This paper presents data on the size, composition and concentration of aerosol particles emitted from north Australian savannah fires and how these properties influence cloud condensation nuclei (CCN) concentrations. Both the size and composition of aerosol were found to be important in determining CCN. Despite large CCNc enhancements during periods of close biomass burning, the aerosol was very weakly hygroscopic which should be accounted for in climate models to avoid large CCNc overestimates.
Xuewu Fu, Xu Yang, Xiaofang Lang, Jun Zhou, Hui Zhang, Ben Yu, Haiyu Yan, Che-Jen Lin, and Xinbin Feng
Atmos. Chem. Phys., 16, 11547–11562, https://doi.org/10.5194/acp-16-11547-2016, https://doi.org/10.5194/acp-16-11547-2016, 2016
Zeyuan Chen, Liang Chu, Edward S. Galbavy, Keren Ram, and Cort Anastasio
Atmos. Chem. Phys., 16, 9579–9590, https://doi.org/10.5194/acp-16-9579-2016, https://doi.org/10.5194/acp-16-9579-2016, 2016
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We made the first measurements of the concentrations of hydroxyl radical (•OH), a dominant environmental oxidant, in snow grains. Concentrations of •OH in snow at Summit, Greenland, are comparable to values reported for midlatitude cloud and fog drops, even though impurity levels in the snow are much lower. At these concentrations, the lifetimes of organics and bromide in Summit snow are approximately 3 days and 7 h, respectively, suggesting that OH is a major oxidant for both species.
Dominik van Pinxteren, Khanneh Wadinga Fomba, Stephan Mertes, Konrad Müller, Gerald Spindler, Johannes Schneider, Taehyoung Lee, Jeffrey L. Collett, and Hartmut Herrmann
Atmos. Chem. Phys., 16, 3185–3205, https://doi.org/10.5194/acp-16-3185-2016, https://doi.org/10.5194/acp-16-3185-2016, 2016
A. J. Boris, T. Lee, T. Park, J. Choi, S. J. Seo, and J. L. Collett Jr.
Atmos. Chem. Phys., 16, 437–453, https://doi.org/10.5194/acp-16-437-2016, https://doi.org/10.5194/acp-16-437-2016, 2016
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Samples of fog water collected in the Yellow Sea during summer 2014 represent fog downwind of polluted regions and provide new insight into the fate of regional emissions. Organic and inorganic components reveal contributions from urban, biogenic, marine, and biomass burning emissions, as well as evidence of aqueous organic processing reactions. Many fog components are products of extensive photochemical aging during multiday transport, including oxidation within wet aerosols or fogs.
Y. W. Liu, Xu-Ri, Y. S. Wang, Y. P. Pan, and S. L. Piao
Atmos. Chem. Phys., 15, 11683–11700, https://doi.org/10.5194/acp-15-11683-2015, https://doi.org/10.5194/acp-15-11683-2015, 2015
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We investigated inorganic N wet deposition at five sites in the Tibetan Plateau (TP). Combining in situ measurements in this and previous studies, the average wet deposition of NH4+-N, NO3--N, and inorganic N in the TP was estimated to be 1.06, 0.51, and 1.58 kg N ha−1 yr−1, respectively. Results suggest that earlier estimations based on chemical transport model simulations and/or limited field measurements likely overestimated substantially the regional inorganic N wet deposition in the TP.
Y. P. Pan and Y. S. Wang
Atmos. Chem. Phys., 15, 951–972, https://doi.org/10.5194/acp-15-951-2015, https://doi.org/10.5194/acp-15-951-2015, 2015
Short summary
Short summary
This paper presents the first concurrent measurements of wet and dry deposition of various trace elements in Northern China, covering an extensive area over 3 years in a global hotspot of air pollution. The unique field data can serve as a sound basis for the validation of regional emission inventories and biogeochemical or atmospheric chemistry models. The findings are very important for policy makers to create legislation to reduce the emissions and protect soil and water from air pollution.
S. Makowski Giannoni, R. Rollenbeck, K. Trachte, and J. Bendix
Atmos. Chem. Phys., 14, 11297–11312, https://doi.org/10.5194/acp-14-11297-2014, https://doi.org/10.5194/acp-14-11297-2014, 2014
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K. M. Mullaugh, J. D. Willey, R. J. Kieber, R. N. Mead, and G. B. Avery Jr.
Atmos. Chem. Phys., 13, 2321–2330, https://doi.org/10.5194/acp-13-2321-2013, https://doi.org/10.5194/acp-13-2321-2013, 2013
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Atmos. Chem. Phys., 12, 9417–9426, https://doi.org/10.5194/acp-12-9417-2012, https://doi.org/10.5194/acp-12-9417-2012, 2012
Y. P. Pan, Y. S. Wang, G. Q. Tang, and D. Wu
Atmos. Chem. Phys., 12, 6515–6535, https://doi.org/10.5194/acp-12-6515-2012, https://doi.org/10.5194/acp-12-6515-2012, 2012
Z. H. Dai, X. B. Feng, J. Sommar, P. Li, and X. W. Fu
Atmos. Chem. Phys., 12, 6207–6218, https://doi.org/10.5194/acp-12-6207-2012, https://doi.org/10.5194/acp-12-6207-2012, 2012
K. E. Altieri, M. G. Hastings, A. J. Peters, and D. M. Sigman
Atmos. Chem. Phys., 12, 3557–3571, https://doi.org/10.5194/acp-12-3557-2012, https://doi.org/10.5194/acp-12-3557-2012, 2012
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Atmos. Chem. Phys., 12, 2025–2035, https://doi.org/10.5194/acp-12-2025-2012, https://doi.org/10.5194/acp-12-2025-2012, 2012
M. A. S. Lombard, J. G. Bryce, H. Mao, and R. Talbot
Atmos. Chem. Phys., 11, 7657–7668, https://doi.org/10.5194/acp-11-7657-2011, https://doi.org/10.5194/acp-11-7657-2011, 2011
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Atmos. Chem. Phys., 11, 3743–3755, https://doi.org/10.5194/acp-11-3743-2011, https://doi.org/10.5194/acp-11-3743-2011, 2011
K. Desboeufs, E. Journet, J.-L. Rajot, S. Chevaillier, S. Triquet, P. Formenti, and A. Zakou
Atmos. Chem. Phys., 10, 9283–9293, https://doi.org/10.5194/acp-10-9283-2010, https://doi.org/10.5194/acp-10-9283-2010, 2010
J. M. Caffrey, W. M. Landing, S. D. Nolek, K. J. Gosnell, S. S. Bagui, and S. C. Bagui
Atmos. Chem. Phys., 10, 5425–5434, https://doi.org/10.5194/acp-10-5425-2010, https://doi.org/10.5194/acp-10-5425-2010, 2010
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Short summary
The results on total mercury (THg) wet deposition flux obtained within the GMOS network have been presented and discussed to understand the atmospheric Hg cycling and its seasonal depositional patterns over the 2011–2015 period. The data set provides new insight into baseline concentrations of THg concentrations in precipitation particularly in regions where wet deposition and atmospheric Hg species were not investigated before, opening the way for additional measurements and modeling studies.
The results on total mercury (THg) wet deposition flux obtained within the GMOS network have...
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