Articles | Volume 18, issue 12
https://doi.org/10.5194/acp-18-8571-2018
© Author(s) 2018. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/acp-18-8571-2018
© Author(s) 2018. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Research article
| 
18 Jun 2018
Research article |
| 18 Jun 2018
| 18 Jun 2018
High summertime aerosol organic functional group concentrations from marine and seabird sources at Ross Island, Antarctica, during AWARE
Scripps Institution of Oceanography, University of California, San Diego,
9500 Gilman Drive, La Jolla, CA 92093, USA
Jeramy Dedrick
Scripps Institution of Oceanography, University of California, San Diego,
9500 Gilman Drive, La Jolla, CA 92093, USA
now at: Texas A&M University, 400 Bizzell St, College Station, TX 77843, USA
Scripps Institution of Oceanography, University of California, San Diego,
9500 Gilman Drive, La Jolla, CA 92093, USA
Gunnar I. Senum
Environmental & Climate Sciences Department, Brookhaven National
Laboratory, Building 815-E, Upton, NY 11973-5000, USA
Janek Uin
Environmental & Climate Sciences Department, Brookhaven National
Laboratory, Building 815-E, Upton, NY 11973-5000, USA
Chongai Kuang
Environmental & Climate Sciences Department, Brookhaven National
Laboratory, Building 815-E, Upton, NY 11973-5000, USA
Stephen R. Springston
Environmental & Climate Sciences Department, Brookhaven National
Laboratory, Building 815-E, Upton, NY 11973-5000, USA
W. Richard Leaitch
Environment and Climate Change Canada (ECCC), Toronto, ON, Canada
Allison C. Aiken
Earth and Environmental Science, Earth Systems Observations, Los Alamos
National Laboratory, Los Alamos, New Mexico, USA
Dan Lubin
Scripps Institution of Oceanography, University of California, San Diego,
9500 Gilman Drive, La Jolla, CA 92093, USA
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Madison L. Ghiz, Ryan C. Scott, Andrew M. Vogelmann, Jan T. M. Lenaerts, Matthew Lazzara, and Dan Lubin
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Yang Wang, Guangjie Zheng, Michael P. Jensen, Daniel A. Knopf, Alexander Laskin, Alyssa A. Matthews, David Mechem, Fan Mei, Ryan Moffet, Arthur J. Sedlacek, John E. Shilling, Stephen Springston, Amy Sullivan, Jason Tomlinson, Daniel Veghte, Rodney Weber, Robert Wood, Maria A. Zawadowicz, and Jian Wang
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Anna L. Hodshire, Emily Ramnarine, Ali Akherati, Matthew L. Alvarado, Delphine K. Farmer, Shantanu H. Jathar, Sonia M. Kreidenweis, Chantelle R. Lonsdale, Timothy B. Onasch, Stephen R. Springston, Jian Wang, Yang Wang, Lawrence I. Kleinman, Arthur J. Sedlacek III, and Jeffrey R. Pierce
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Franziska Köllner, Johannes Schneider, Megan D. Willis, Hannes Schulz, Daniel Kunkel, Heiko Bozem, Peter Hoor, Thomas Klimach, Frank Helleis, Julia Burkart, W. Richard Leaitch, Amir A. Aliabadi, Jonathan P. D. Abbatt, Andreas B. Herber, and Stephan Borrmann
Atmos. Chem. Phys., 21, 6509–6539, https://doi.org/10.5194/acp-21-6509-2021, https://doi.org/10.5194/acp-21-6509-2021, 2021
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We present in situ observations of vertically resolved particle chemical composition in the summertime Arctic lower troposphere. Our analysis demonstrates the strong vertical contrast between particle properties within the boundary layer and aloft. Emissions from vegetation fires and anthropogenic sources in northern Canada, Europe, and East Asia influenced particle composition in the free troposphere. Organics detected in Arctic aerosol particles can partly be identified as dicarboxylic acids.
Kevin J. Sanchez, Gregory C. Roberts, Georges Saliba, Lynn M. Russell, Cynthia Twohy, J. Michael Reeves, Ruhi S. Humphries, Melita D. Keywood, Jason P. Ward, and Ian M. McRobert
Atmos. Chem. Phys., 21, 3427–3446, https://doi.org/10.5194/acp-21-3427-2021, https://doi.org/10.5194/acp-21-3427-2021, 2021
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Betty Croft, Randall V. Martin, Richard H. Moore, Luke D. Ziemba, Ewan C. Crosbie, Hongyu Liu, Lynn M. Russell, Georges Saliba, Armin Wisthaler, Markus Müller, Arne Schiller, Martí Galí, Rachel Y.-W. Chang, Erin E. McDuffie, Kelsey R. Bilsback, and Jeffrey R. Pierce
Atmos. Chem. Phys., 21, 1889–1916, https://doi.org/10.5194/acp-21-1889-2021, https://doi.org/10.5194/acp-21-1889-2021, 2021
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Kevin J. Sanchez, Bo Zhang, Hongyu Liu, Georges Saliba, Chia-Li Chen, Savannah L. Lewis, Lynn M. Russell, Michael A. Shook, Ewan C. Crosbie, Luke D. Ziemba, Matthew D. Brown, Taylor J. Shingler, Claire E. Robinson, Elizabeth B. Wiggins, Kenneth L. Thornhill, Edward L. Winstead, Carolyn Jordan, Patricia K. Quinn, Timothy S. Bates, Jack Porter, Thomas G. Bell, Eric S. Saltzman, Michael J. Behrenfeld, and Richard H. Moore
Atmos. Chem. Phys., 21, 831–851, https://doi.org/10.5194/acp-21-831-2021, https://doi.org/10.5194/acp-21-831-2021, 2021
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Models describing atmospheric airflow were combined with satellite measurements representative of marine phytoplankton and other meteorological variables. These combined variables were compared to measured aerosol to identify upwind influences on aerosol concentrations. Results indicate that phytoplankton production rates upwind impact the aerosol mass. Also, results suggest that the condensation of mass onto short-lived large sea spray particles may be a significant sink of aerosol mass.
Michael J. Lawler, Savannah L. Lewis, Lynn M. Russell, Patricia K. Quinn, Timothy S. Bates, Derek J. Coffman, Lucia M. Upchurch, and Eric S. Saltzman
Atmos. Chem. Phys., 20, 16007–16022, https://doi.org/10.5194/acp-20-16007-2020, https://doi.org/10.5194/acp-20-16007-2020, 2020
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Lawrence I. Kleinman, Arthur J. Sedlacek III, Kouji Adachi, Peter R. Buseck, Sonya Collier, Manvendra K. Dubey, Anna L. Hodshire, Ernie Lewis, Timothy B. Onasch, Jeffery R. Pierce, John Shilling, Stephen R. Springston, Jian Wang, Qi Zhang, Shan Zhou, and Robert J. Yokelson
Atmos. Chem. Phys., 20, 13319–13341, https://doi.org/10.5194/acp-20-13319-2020, https://doi.org/10.5194/acp-20-13319-2020, 2020
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Aerosols from wildfires affect the Earth's temperature by absorbing light or reflecting it back into space. This study investigates time-dependent chemical, microphysical, and optical properties of aerosols generated by wildfires in the Pacific Northwest, USA. Wildfire smoke plumes were traversed by an instrumented aircraft at locations near the fire and up to 3.5 h travel time downwind. Although there was no net aerosol production, aerosol particles grew and became more efficient scatters.
Guangjie Zheng, Chongai Kuang, Janek Uin, Thomas Watson, and Jian Wang
Atmos. Chem. Phys., 20, 12515–12525, https://doi.org/10.5194/acp-20-12515-2020, https://doi.org/10.5194/acp-20-12515-2020, 2020
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Condensational growth of Aitken-mode particles is a major source of cloud condensation nuclei in the remote marine boundary layer. It has been long thought that over remote oceans, condensation growth is dominated by sulfate that derives from ocean-emitted dimethyl sulfide. In this study, we present the first long-term observational evidence that, contrary to conventional thinking, organics play an even more important role than sulfate in particle growth over remote oceans throughout the year.
W. Richard Leaitch, John K. Kodros, Megan D. Willis, Sarah Hanna, Hannes Schulz, Elisabeth Andrews, Heiko Bozem, Julia Burkart, Peter Hoor, Felicia Kolonjari, John A. Ogren, Sangeeta Sharma, Meng Si, Knut von Salzen, Allan K. Bertram, Andreas Herber, Jonathan P. D. Abbatt, and Jeffrey R. Pierce
Atmos. Chem. Phys., 20, 10545–10563, https://doi.org/10.5194/acp-20-10545-2020, https://doi.org/10.5194/acp-20-10545-2020, 2020
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Luke T. Cravigan, Marc D. Mallet, Petri Vaattovaara, Mike J. Harvey, Cliff S. Law, Robin L. Modini, Lynn M. Russell, Ed Stelcer, David D. Cohen, Greg Olsen, Karl Safi, Timothy J. Burrell, and Zoran Ristovski
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Aerosol–cloud interactions in remote marine environments are poorly represented in atmospheric modelling, particularly over the Southern Hemisphere. This work reports in situ chamber observations of sea spray aerosol composition and water uptake during the Surface Ocean Aerosol Production (SOAP) voyage. Observations were compared with currently applied models for sea spray organic enrichment. The sea spray hygroscopicity was persistently high, even at high organic fractions.
Francesca Gallo, Janek Uin, Stephen Springston, Jian Wang, Guangjie Zheng, Chongai Kuang, Robert Wood, Eduardo B. Azevedo, Allison McComiskey, Fan Mei, Adam Theisen, Jenni Kyrouac, and Allison C. Aiken
Atmos. Chem. Phys., 20, 7553–7573, https://doi.org/10.5194/acp-20-7553-2020, https://doi.org/10.5194/acp-20-7553-2020, 2020
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Continuous high-time-resolution ambient data can include periods when aerosol properties do not represent regional aerosol processes due to high-concentration local events. We develop a novel aerosol mask at the U.S. Department of Energy’s Atmospheric Radiation Measurement (ARM) facility in the eastern North Atlantic (ENA). We use two ground sites to validate the mask, include a comparison with aircraft overflights, and provide guidance to increase data quality at ENA and other locations.
Fan Mei, Jian Wang, Jennifer M. Comstock, Ralf Weigel, Martina Krämer, Christoph Mahnke, John E. Shilling, Johannes Schneider, Christiane Schulz, Charles N. Long, Manfred Wendisch, Luiz A. T. Machado, Beat Schmid, Trismono Krisna, Mikhail Pekour, John Hubbe, Andreas Giez, Bernadett Weinzierl, Martin Zoeger, Mira L. Pöhlker, Hans Schlager, Micael A. Cecchini, Meinrat O. Andreae, Scot T. Martin, Suzane S. de Sá, Jiwen Fan, Jason Tomlinson, Stephen Springston, Ulrich Pöschl, Paulo Artaxo, Christopher Pöhlker, Thomas Klimach, Andreas Minikin, Armin Afchine, and Stephan Borrmann
Atmos. Meas. Tech., 13, 661–684, https://doi.org/10.5194/amt-13-661-2020, https://doi.org/10.5194/amt-13-661-2020, 2020
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In 2014, the US DOE G1 aircraft and the German HALO aircraft overflew the Amazon basin to study how aerosols influence cloud cycles under a clean condition and around a tropical megacity. This paper describes how to meaningfully compare similar measurements from two research aircraft and identify the potential measurement issue. We also discuss the uncertainty range for each measurement for further usage in model evaluation and satellite data validation.
Joelle Dionne, Knut von Salzen, Jason Cole, Rashed Mahmood, W. Richard Leaitch, Glen Lesins, Ian Folkins, and Rachel Y.-W. Chang
Atmos. Chem. Phys., 20, 29–43, https://doi.org/10.5194/acp-20-29-2020, https://doi.org/10.5194/acp-20-29-2020, 2020
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Low clouds persist in the summer Arctic, with important consequences for the radiation budget. We found that the ability of precipitation parameterizations to reproduce observed cloud properties was more variable than their ability to represent radiative effects. Our results show that cloud properties and their parameterizations affect the radiative effects of clouds.
Heiko Bozem, Peter Hoor, Daniel Kunkel, Franziska Köllner, Johannes Schneider, Andreas Herber, Hannes Schulz, W. Richard Leaitch, Amir A. Aliabadi, Megan D. Willis, Julia Burkart, and Jonathan P. D. Abbatt
Atmos. Chem. Phys., 19, 15049–15071, https://doi.org/10.5194/acp-19-15049-2019, https://doi.org/10.5194/acp-19-15049-2019, 2019
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We present airborne trace gas measurements in the European and Canadian Arctic for July 2014 and April 2015. Based on CO and CO2 in situ data as well as 10 d kinematic back trajectories, we characterize the prevailing transport regimes and derive a tracer-based diagnostic for the determination of the polar dome boundary. Using the tracer-derived boundary, an analysis of the recent transport history of air masses within the polar dome reveals significant differences between spring and summer.
Roya Ghahreman, Wanmin Gong, Martí Galí, Ann-Lise Norman, Stephen R. Beagley, Ayodeji Akingunola, Qiong Zheng, Alexandru Lupu, Martine Lizotte, Maurice Levasseur, and W. Richard Leaitch
Atmos. Chem. Phys., 19, 14455–14476, https://doi.org/10.5194/acp-19-14455-2019, https://doi.org/10.5194/acp-19-14455-2019, 2019
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Atmospheric DMS(g) is a climatically important compound and the main source of biogenic sulfate in the Arctic. Its abundance in the Arctic increases during summer due to greater ice-free sea surface and higher biological activity. In this study, we implemented DMS(g) in a regional air quality forecast model configured for the Arctic. The study showed a significant impact from DMS(g) on sulfate aerosols, particularly in the 50–100 nm size range, in the Arctic marine boundary layer during summer.
Keith M. Hines, David H. Bromwich, Sheng-Hung Wang, Israel Silber, Johannes Verlinde, and Dan Lubin
Atmos. Chem. Phys., 19, 12431–12454, https://doi.org/10.5194/acp-19-12431-2019, https://doi.org/10.5194/acp-19-12431-2019, 2019
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We explore how well clouds are represented in numerical weather prediction over Antarctica, a very difficult environment for field programs where few studies have been conducted. Fortunately, a 2015–2017 field program for West Antarctica supplied observations. We achieve promising results with newer, more advanced cloud schemes. We need to understand the role of clouds and precipitation in the maintenance of the Antarctic ice mass to understand and predict sea level change over the 21st century.
Suzane S. de Sá, Luciana V. Rizzo, Brett B. Palm, Pedro Campuzano-Jost, Douglas A. Day, Lindsay D. Yee, Rebecca Wernis, Gabriel Isaacman-VanWertz, Joel Brito, Samara Carbone, Yingjun J. Liu, Arthur Sedlacek, Stephen Springston, Allen H. Goldstein, Henrique M. J. Barbosa, M. Lizabeth Alexander, Paulo Artaxo, Jose L. Jimenez, and Scot T. Martin
Atmos. Chem. Phys., 19, 7973–8001, https://doi.org/10.5194/acp-19-7973-2019, https://doi.org/10.5194/acp-19-7973-2019, 2019
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This study investigates the impacts of urban and fire emissions on the concentration, composition, and optical properties of submicron particulate matter (PM1) in central Amazonia during the dry season. Biomass-burning and urban emissions appeared to contribute at least 80 % of brown carbon absorption while accounting for 30 % to 40 % of the organic PM1 mass concentration. Only a fraction of the 9-fold increase in mass concentration relative to the wet season was due to biomass burning.
Samantha Tremblay, Jean-Christophe Picard, Jill O. Bachelder, Erik Lutsch, Kimberly Strong, Pierre Fogal, W. Richard Leaitch, Sangeeta Sharma, Felicia Kolonjari, Christopher J. Cox, Rachel Y.-W. Chang, and Patrick L. Hayes
Atmos. Chem. Phys., 19, 5589–5604, https://doi.org/10.5194/acp-19-5589-2019, https://doi.org/10.5194/acp-19-5589-2019, 2019
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Atmospheric aerosols, tiny airborne particles, have an important impact on climate. However, a lack of understanding of the chemistry of aerosols is one of the largest contributors to uncertainty in predictions of climate change. Measurements of aerosols were carried out in the Arctic at Eureka Station, Canada, to better understand what role aerosols play in this fragile environment. It is found that organic aerosols, possibly originating from marine emissions, are ubiquitous during summertime.
Meng Si, Erin Evoy, Jingwei Yun, Yu Xi, Sarah J. Hanna, Alina Chivulescu, Kevin Rawlings, Daniel Veber, Andrew Platt, Daniel Kunkel, Peter Hoor, Sangeeta Sharma, W. Richard Leaitch, and Allan K. Bertram
Atmos. Chem. Phys., 19, 3007–3024, https://doi.org/10.5194/acp-19-3007-2019, https://doi.org/10.5194/acp-19-3007-2019, 2019
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We investigated the importance of mineral dust, sea spray aerosol, and anthropogenic aerosol to the ice-nucleating particle (INP) population in the Canadian Arctic during spring 2016. The results suggest that mineral dust transported from the Gobi Desert was a major source of the INP population studied, and that sea spray aerosol decreased the ice-nucleating ability of mineral dust. The results should be useful for testing and improving models used to predict INPs and climate in the Arctic.
Betty Croft, Randall V. Martin, W. Richard Leaitch, Julia Burkart, Rachel Y.-W. Chang, Douglas B. Collins, Patrick L. Hayes, Anna L. Hodshire, Lin Huang, John K. Kodros, Alexander Moravek, Emma L. Mungall, Jennifer G. Murphy, Sangeeta Sharma, Samantha Tremblay, Gregory R. Wentworth, Megan D. Willis, Jonathan P. D. Abbatt, and Jeffrey R. Pierce
Atmos. Chem. Phys., 19, 2787–2812, https://doi.org/10.5194/acp-19-2787-2019, https://doi.org/10.5194/acp-19-2787-2019, 2019
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Summertime Arctic atmospheric aerosols are strongly controlled by processes related to natural regional sources. We use a chemical transport model with size-resolved aerosol microphysics to interpret measurements made during summertime 2016 in the Canadian Arctic Archipelago. Our results explore the processes that control summertime aerosol size distributions and support a climate-relevant role for Arctic marine secondary organic aerosol formed from precursor vapors with Arctic marine sources.
Jonathan P. D. Abbatt, W. Richard Leaitch, Amir A. Aliabadi, Allan K. Bertram, Jean-Pierre Blanchet, Aude Boivin-Rioux, Heiko Bozem, Julia Burkart, Rachel Y. W. Chang, Joannie Charette, Jai P. Chaubey, Robert J. Christensen, Ana Cirisan, Douglas B. Collins, Betty Croft, Joelle Dionne, Greg J. Evans, Christopher G. Fletcher, Martí Galí, Roya Ghahreman, Eric Girard, Wanmin Gong, Michel Gosselin, Margaux Gourdal, Sarah J. Hanna, Hakase Hayashida, Andreas B. Herber, Sareh Hesaraki, Peter Hoor, Lin Huang, Rachel Hussherr, Victoria E. Irish, Setigui A. Keita, John K. Kodros, Franziska Köllner, Felicia Kolonjari, Daniel Kunkel, Luis A. Ladino, Kathy Law, Maurice Levasseur, Quentin Libois, John Liggio, Martine Lizotte, Katrina M. Macdonald, Rashed Mahmood, Randall V. Martin, Ryan H. Mason, Lisa A. Miller, Alexander Moravek, Eric Mortenson, Emma L. Mungall, Jennifer G. Murphy, Maryam Namazi, Ann-Lise Norman, Norman T. O'Neill, Jeffrey R. Pierce, Lynn M. Russell, Johannes Schneider, Hannes Schulz, Sangeeta Sharma, Meng Si, Ralf M. Staebler, Nadja S. Steiner, Jennie L. Thomas, Knut von Salzen, Jeremy J. B. Wentzell, Megan D. Willis, Gregory R. Wentworth, Jun-Wei Xu, and Jacqueline D. Yakobi-Hancock
Atmos. Chem. Phys., 19, 2527–2560, https://doi.org/10.5194/acp-19-2527-2019, https://doi.org/10.5194/acp-19-2527-2019, 2019
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The Arctic is experiencing considerable environmental change with climate warming, illustrated by the dramatic decrease in sea-ice extent. It is important to understand both the natural and perturbed Arctic systems to gain a better understanding of how they will change in the future. This paper summarizes new insights into the relationships between Arctic aerosol particles and climate, as learned over the past five or so years by a large Canadian research consortium, NETCARE.
Hannes Schulz, Marco Zanatta, Heiko Bozem, W. Richard Leaitch, Andreas B. Herber, Julia Burkart, Megan D. Willis, Daniel Kunkel, Peter M. Hoor, Jonathan P. D. Abbatt, and Rüdiger Gerdes
Atmos. Chem. Phys., 19, 2361–2384, https://doi.org/10.5194/acp-19-2361-2019, https://doi.org/10.5194/acp-19-2361-2019, 2019
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Aircraft vertical profiles of black carbon (BC) aerosol from the High Canadian Arctic have shown systematic variability in different levels of the cold, stably stratified polar dome. During spring and summer, efficiencies of BC supply by transport (often from gas flaring and wildfire-affected regions) were different in the lower dome than at higher levels, as apparent from changes in mean particle size and mixing ratios with CO. Summer BC concentrations were a factor of 10 lower than in spring.
Victoria E. Irish, Sarah J. Hanna, Megan D. Willis, Swarup China, Jennie L. Thomas, Jeremy J. B. Wentzell, Ana Cirisan, Meng Si, W. Richard Leaitch, Jennifer G. Murphy, Jonathan P. D. Abbatt, Alexander Laskin, Eric Girard, and Allan K. Bertram
Atmos. Chem. Phys., 19, 1027–1039, https://doi.org/10.5194/acp-19-1027-2019, https://doi.org/10.5194/acp-19-1027-2019, 2019
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Ice nucleating particles (INPs) are atmospheric particles that catalyse the formation of ice crystals in clouds. INPs influence the Earth's radiative balance and hydrological cycle. In this study we measured the concentrations of INPs in the Canadian Arctic marine boundary layer. Average INP concentrations fell within the range measured in other marine boundary layer locations. We also found that mineral dust is a more important contributor to the INP population than sea spray aerosol.
Megan D. Willis, Heiko Bozem, Daniel Kunkel, Alex K. Y. Lee, Hannes Schulz, Julia Burkart, Amir A. Aliabadi, Andreas B. Herber, W. Richard Leaitch, and Jonathan P. D. Abbatt
Atmos. Chem. Phys., 19, 57–76, https://doi.org/10.5194/acp-19-57-2019, https://doi.org/10.5194/acp-19-57-2019, 2019
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The vertical distribution of Arctic aerosol is an important driver of its climate impacts. We present vertically resolved measurements of aerosol composition and properties made in the High Arctic during spring on an aircraft platform. We explore how aerosol properties are related to transport history and show evidence of vertical trends in aerosol sources, transport mechanisms and composition. These results will help us to better understand aerosol–climate interactions in the Arctic.
Johannes Mülmenstädt, Odran Sourdeval, David S. Henderson, Tristan S. L'Ecuyer, Claudia Unglaub, Leonore Jungandreas, Christoph Böhm, Lynn M. Russell, and Johannes Quaas
Earth Syst. Sci. Data, 10, 2279–2293, https://doi.org/10.5194/essd-10-2279-2018, https://doi.org/10.5194/essd-10-2279-2018, 2018
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One of the key pieces of information about a cloud is how high its base is. Unlike cloud top, cloud base is hard to observe from a satellite perspective – the cloud blocks the view. But without using satellites, it is difficult to compile global datasets. Here we describe how we worked around the limitations of a cloud-detecting laser satellite to observe global cloud base heights. This dataset will expand our knowledge of the cloudy atmosphere and its interaction with the planetary surface.
Guangjie Zheng, Yang Wang, Allison C. Aiken, Francesca Gallo, Michael P. Jensen, Pavlos Kollias, Chongai Kuang, Edward Luke, Stephen Springston, Janek Uin, Robert Wood, and Jian Wang
Atmos. Chem. Phys., 18, 17615–17635, https://doi.org/10.5194/acp-18-17615-2018, https://doi.org/10.5194/acp-18-17615-2018, 2018
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Here, we elucidate the key processes that drive marine boundary layer (MBL) aerosol size distribution in the eastern North Atlantic (ENA) using long-term measurements. The governing equations of particle concentration are established for different modes. Particles entrained from the free troposphere represent the major source of MBL cloud condensation nuclei (CCN), contributing both directly to CCN population and indirectly by supplying Aitken-mode particles that grow to CCN in the MBL.
Tuomo Nieminen, Veli-Matti Kerminen, Tuukka Petäjä, Pasi P. Aalto, Mikhail Arshinov, Eija Asmi, Urs Baltensperger, David C. S. Beddows, Johan Paul Beukes, Don Collins, Aijun Ding, Roy M. Harrison, Bas Henzing, Rakesh Hooda, Min Hu, Urmas Hõrrak, Niku Kivekäs, Kaupo Komsaare, Radovan Krejci, Adam Kristensson, Lauri Laakso, Ari Laaksonen, W. Richard Leaitch, Heikki Lihavainen, Nikolaos Mihalopoulos, Zoltán Németh, Wei Nie, Colin O'Dowd, Imre Salma, Karine Sellegri, Birgitta Svenningsson, Erik Swietlicki, Peter Tunved, Vidmantas Ulevicius, Ville Vakkari, Marko Vana, Alfred Wiedensohler, Zhijun Wu, Annele Virtanen, and Markku Kulmala
Atmos. Chem. Phys., 18, 14737–14756, https://doi.org/10.5194/acp-18-14737-2018, https://doi.org/10.5194/acp-18-14737-2018, 2018
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Atmospheric aerosols have diverse effects on air quality, human health, and global climate. One important source of aerosols is their formation via nucleation and growth in the atmosphere. We have analyzed long-term observations of regional new particle formation events around the globe and provide a comprehensive view on the characteristics of this phenomenon in diverse environments. The results are useful in developing more realistic representation of atmospheric aerosols in global models.
Daniela Wimmer, Stephany Buenrostro Mazon, Hanna Elina Manninen, Juha Kangasluoma, Alessandro Franchin, Tuomo Nieminen, John Backman, Jian Wang, Chongai Kuang, Radovan Krejci, Joel Brito, Fernando Goncalves Morais, Scot Turnbull Martin, Paulo Artaxo, Markku Kulmala, Veli-Matti Kerminen, and Tuukka Petäjä
Atmos. Chem. Phys., 18, 13245–13264, https://doi.org/10.5194/acp-18-13245-2018, https://doi.org/10.5194/acp-18-13245-2018, 2018
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This work focuses on understanding the production of very small airborne particles in the undisturbed environment of the Amazon basin. Computer models have shown that up to 70 % of these tiny particles are responsible for cloud formation on a global scale. The processes behind the production of these very small particles have been studied intensely recently. Their appearance has been observed almost all over the world. We directly measure sub-3 nm aerosols for the first time in the Amazon basin.
John K. Kodros, Sarah J. Hanna, Allan K. Bertram, W. Richard Leaitch, Hannes Schulz, Andreas B. Herber, Marco Zanatta, Julia Burkart, Megan D. Willis, Jonathan P. D. Abbatt, and Jeffrey R. Pierce
Atmos. Chem. Phys., 18, 11345–11361, https://doi.org/10.5194/acp-18-11345-2018, https://doi.org/10.5194/acp-18-11345-2018, 2018
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The mixing state of black carbon is one of the key uncertainties limiting the ability of models to estimate the direct radiative effect. In this work, we present aircraft measurements from the Canadian Arctic of coating thickness as a function of black carbon core diameter and black-carbon-containing particle number fractions. We use these measurements to inform estimates of the direct radiative effect in Arctic aerosol simulations.
Arthur J. Sedlacek III, Peter R. Buseck, Kouji Adachi, Timothy B. Onasch, Stephen R. Springston, and Lawrence Kleinman
Atmos. Chem. Phys., 18, 11289–11301, https://doi.org/10.5194/acp-18-11289-2018, https://doi.org/10.5194/acp-18-11289-2018, 2018
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This paper presents the first direct atmospheric observations of the formation and evolution of tar balls (TBs) in forest fires collected during the Department of Energy’s Biomass Burning Observation Project (BBOP). We quantify, for the first time, the TB mass fraction in the BB plumes and show that this mass fraction increases from less than 1 % to 50 % within the first couple of hours of plume aging. Using Mie theory we find that TBs are consistent with being weak light absorbers.
John E. Shilling, Mikhail S. Pekour, Edward C. Fortner, Paulo Artaxo, Suzane de Sá, John M. Hubbe, Karla M. Longo, Luiz A. T. Machado, Scot T. Martin, Stephen R. Springston, Jason Tomlinson, and Jian Wang
Atmos. Chem. Phys., 18, 10773–10797, https://doi.org/10.5194/acp-18-10773-2018, https://doi.org/10.5194/acp-18-10773-2018, 2018
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We report aircraft observations of the evolution of organic aerosol in the Manaus urban plume as it ages. We observe dynamic changes in the organic aerosol. The mean carbon oxidation state of the OA increases from −0.6 to −0.45. Hydrocarbon-like organic aerosol (HOA) mass is lost and is balanced out by formation of oxygenated organic aerosol (OOA). Because HOA loss is balanced by OOA formation, we observe little change in the net Δorg / ΔCO values with aging.
Katrina M. Macdonald, Sangeeta Sharma, Desiree Toom, Alina Chivulescu, Andrew Platt, Mike Elsasser, Lin Huang, Richard Leaitch, Nathan Chellman, Joseph R. McConnell, Heiko Bozem, Daniel Kunkel, Ying Duan Lei, Cheol-Heon Jeong, Jonathan P. D. Abbatt, and Greg J. Evans
Atmos. Chem. Phys., 18, 3485–3503, https://doi.org/10.5194/acp-18-3485-2018, https://doi.org/10.5194/acp-18-3485-2018, 2018
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The sources of key contaminants in Arctic snow may be an important factor in understanding the rapid climate changes observed in the Arctic. Fresh snow samples collected frequently through the winter season were analyzed for major constituents. Temporally refined source apportionment via positive matrix factorization in conjunction with FLEXPART suggested potential source characteristics and locations. The identity of these sources and their relative contribution to key analytes is discussed.
W. Richard Leaitch, Lynn M. Russell, Jun Liu, Felicia Kolonjari, Desiree Toom, Lin Huang, Sangeeta Sharma, Alina Chivulescu, Dan Veber, and Wendy Zhang
Atmos. Chem. Phys., 18, 3269–3287, https://doi.org/10.5194/acp-18-3269-2018, https://doi.org/10.5194/acp-18-3269-2018, 2018
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Over 2 years of atmospheric aerosol organic functional group and microphysics measurements at the world's northernmost land observatory offer a unique high-latitude dataset. Lower organic mass (OM) concentrations and higher OM fractions accompany smaller particles during summer, with opposite results during winter to spring. Seasonally, the OM oxidation level is highest in winter, associated with primary marine alcohol groups. In summer, secondary processes dominate the marine influence on OM.
Brett B. Palm, Suzane S. de Sá, Douglas A. Day, Pedro Campuzano-Jost, Weiwei Hu, Roger Seco, Steven J. Sjostedt, Jeong-Hoo Park, Alex B. Guenther, Saewung Kim, Joel Brito, Florian Wurm, Paulo Artaxo, Ryan Thalman, Jian Wang, Lindsay D. Yee, Rebecca Wernis, Gabriel Isaacman-VanWertz, Allen H. Goldstein, Yingjun Liu, Stephen R. Springston, Rodrigo Souza, Matt K. Newburn, M. Lizabeth Alexander, Scot T. Martin, and Jose L. Jimenez
Atmos. Chem. Phys., 18, 467–493, https://doi.org/10.5194/acp-18-467-2018, https://doi.org/10.5194/acp-18-467-2018, 2018
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Ambient air was oxidized by OH or O3 in an oxidation flow reactor during both wet and dry seasons in the GoAmazon2014/5 campaign to study secondary organic aerosol (SOA) formation. We investigated how much biogenic, urban, and biomass burning sources contributed to the ambient concentrations of SOA precursor gases and how their contributions changed diurnally and seasonally. SOA yields and hygroscopicity of organic aerosol in the oxidation flow reactor were also studied.
Sangeeta Sharma, W. Richard Leaitch, Lin Huang, Daniel Veber, Felicia Kolonjari, Wendy Zhang, Sarah J. Hanna, Allan K. Bertram, and John A. Ogren
Atmos. Chem. Phys., 17, 15225–15243, https://doi.org/10.5194/acp-17-15225-2017, https://doi.org/10.5194/acp-17-15225-2017, 2017
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A new and unique data set on BC properties at the highest latitude observatory in the world, at Alert, Canada, evaluates three techniques for estimating black carbon (BC) and gives seasonal best estimates of the BC mass concentrations and BC mass absorption coefficients (MAC) for 2.5 years of data. As a short-lived climate forcer, better estimates of the properties of BC are necessary to ensure accurate modelling of aerosol climate forcing of the Arctic atmosphere for mitigation purposes.
Alex K. Y. Lee, Chia-Li Chen, Jun Liu, Derek J. Price, Raghu Betha, Lynn M. Russell, Xiaolu Zhang, and Christopher D. Cappa
Atmos. Chem. Phys., 17, 15055–15067, https://doi.org/10.5194/acp-17-15055-2017, https://doi.org/10.5194/acp-17-15055-2017, 2017
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Understanding the mixing state of ambient black carbon (BC) and the chemical characteristics of its associated coatings is important to evaluate BC fate and environmental impacts. This study reports fresh secondary organic aerosol (SOA) formation near traffic emissions during daytime. Our observations suggest that BC was unlikely the major condensation sink of SOA, and a portion of SOA condensed on BC surface was chemically different from other SOA particles that were externally mixed with BC.
Franziska Köllner, Johannes Schneider, Megan D. Willis, Thomas Klimach, Frank Helleis, Heiko Bozem, Daniel Kunkel, Peter Hoor, Julia Burkart, W. Richard Leaitch, Amir A. Aliabadi, Jonathan P. D. Abbatt, Andreas B. Herber, and Stephan Borrmann
Atmos. Chem. Phys., 17, 13747–13766, https://doi.org/10.5194/acp-17-13747-2017, https://doi.org/10.5194/acp-17-13747-2017, 2017
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We conducted aircraft-based single particle chemical composition measurements in the Canadian high Arctic during summer. Our results provide evidence for a marine-biogenic influence on secondary formation of particulate trimethylamine in the Arctic boundary layer. Understanding emission sources and further processes controlling aerosol number concentration and chemical composition in the pristine Arctic summer is crucial for modeling future climate in the area.
Ryan Thalman, Suzane S. de Sá, Brett B. Palm, Henrique M. J. Barbosa, Mira L. Pöhlker, M. Lizabeth Alexander, Joel Brito, Samara Carbone, Paulo Castillo, Douglas A. Day, Chongai Kuang, Antonio Manzi, Nga Lee Ng, Arthur J. Sedlacek III, Rodrigo Souza, Stephen Springston, Thomas Watson, Christopher Pöhlker, Ulrich Pöschl, Meinrat O. Andreae, Paulo Artaxo, Jose L. Jimenez, Scot T. Martin, and Jian Wang
Atmos. Chem. Phys., 17, 11779–11801, https://doi.org/10.5194/acp-17-11779-2017, https://doi.org/10.5194/acp-17-11779-2017, 2017
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Particle hygroscopicity, mixing state, and the hygroscopicity of organic components were characterized in central Amazonia for 1 year; their seasonal and diel variations were driven by a combination of primary emissions, photochemical oxidation, and boundary layer development. The relationship between the hygroscopicity of organic components and their oxidation level was examined, and the results help to reconcile the differences among the relationships observed in previous studies.
Benjamin N. Murphy, Matthew C. Woody, Jose L. Jimenez, Ann Marie G. Carlton, Patrick L. Hayes, Shang Liu, Nga L. Ng, Lynn M. Russell, Ari Setyan, Lu Xu, Jeff Young, Rahul A. Zaveri, Qi Zhang, and Havala O. T. Pye
Atmos. Chem. Phys., 17, 11107–11133, https://doi.org/10.5194/acp-17-11107-2017, https://doi.org/10.5194/acp-17-11107-2017, 2017
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We incorporate recent findings about the behavior of organic pollutants in urban airsheds into the Community Multiscale Air Quality (CMAQ) model to refine predictions of organic particulate pollution in the United States. The new techniques, which account for the volatility and ongoing chemistry of airborne organic compounds, substantially reduce biases, particularly in the winter time and near emission sources.
Kevin J. Sanchez, Gregory C. Roberts, Radiance Calmer, Keri Nicoll, Eyal Hashimshoni, Daniel Rosenfeld, Jurgita Ovadnevaite, Jana Preissler, Darius Ceburnis, Colin O'Dowd, and Lynn M. Russell
Atmos. Chem. Phys., 17, 9797–9814, https://doi.org/10.5194/acp-17-9797-2017, https://doi.org/10.5194/acp-17-9797-2017, 2017
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Unmanned aerial vehicles are equipped with meteorological sensors to measure cloud properties. The measurements are used to calculate the amount of solar radiation reflected by the clouds and compared to simulation results. The uncertainties related to radiative forcing in the simulations are from the lack of mixing in the boundary layer and mixing of dry air into the cloud top. Conservative variables are used to calculate the amount of air mixed into cloud top to minimize these uncertainties.
Roya Ghahreman, Ann-Lise Norman, Betty Croft, Randall V. Martin, Jeffrey R. Pierce, Julia Burkart, Ofelia Rempillo, Heiko Bozem, Daniel Kunkel, Jennie L. Thomas, Amir A. Aliabadi, Gregory R. Wentworth, Maurice Levasseur, Ralf M. Staebler, Sangeeta Sharma, and W. Richard Leaitch
Atmos. Chem. Phys., 17, 8757–8770, https://doi.org/10.5194/acp-17-8757-2017, https://doi.org/10.5194/acp-17-8757-2017, 2017
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We present spring and summertime vertical profile measurements of Arctic dimethyl sulfide (DMS), together with model simulations to consider what these profiles indicate about DMS sources and lifetimes in the Arctic. Our results highlight the role of local open water as the source of DMS(g) during July 2014 and the influence of long-range transport of DMS(g) from further afield in the Arctic during April 2015.
Suzane S. de Sá, Brett B. Palm, Pedro Campuzano-Jost, Douglas A. Day, Matthew K. Newburn, Weiwei Hu, Gabriel Isaacman-VanWertz, Lindsay D. Yee, Ryan Thalman, Joel Brito, Samara Carbone, Paulo Artaxo, Allen H. Goldstein, Antonio O. Manzi, Rodrigo A. F. Souza, Fan Mei, John E. Shilling, Stephen R. Springston, Jian Wang, Jason D. Surratt, M. Lizabeth Alexander, Jose L. Jimenez, and Scot T. Martin
Atmos. Chem. Phys., 17, 6611–6629, https://doi.org/10.5194/acp-17-6611-2017, https://doi.org/10.5194/acp-17-6611-2017, 2017
Julia Burkart, Megan D. Willis, Heiko Bozem, Jennie L. Thomas, Kathy Law, Peter Hoor, Amir A. Aliabadi, Franziska Köllner, Johannes Schneider, Andreas Herber, Jonathan P. D. Abbatt, and W. Richard Leaitch
Atmos. Chem. Phys., 17, 5515–5535, https://doi.org/10.5194/acp-17-5515-2017, https://doi.org/10.5194/acp-17-5515-2017, 2017
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Our aircraft study for the first time systematically investigates aerosol size distributions, including ultrafine particles (5–20 nm in diameter), in the Arctic summertime atmosphere. We find that ultrafine particles occur very frequently in the boundary layer and not aloft, suggesting a surface source of these particles. Understanding aerosol properties and sources is crucial to predict climate and especially important in the Arctic as this region responds extremely fast to climate change.
Andrew D. Teakles, Rita So, Bruce Ainslie, Robert Nissen, Corinne Schiller, Roxanne Vingarzan, Ian McKendry, Anne Marie Macdonald, Daniel A. Jaffe, Allan K. Bertram, Kevin B. Strawbridge, W. Richard Leaitch, Sarah Hanna, Desiree Toom, Jonathan Baik, and Lin Huang
Atmos. Chem. Phys., 17, 2593–2611, https://doi.org/10.5194/acp-17-2593-2017, https://doi.org/10.5194/acp-17-2593-2017, 2017
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We present a case study of an intense wildfire smoke plume from Siberia that affected the air quality across the Pacific Northwest on 6–10 July 2012. The transport, entrainment, and chemical composition of the plume are examined to characterize the event. Ambient O3 and PM2.5 from surface monitoring is contrast to modelled baseline air quality estimates to show the overall contribution of the plume to exceedances in O3 and PM2.5 air quality standards and objectives that occurred.
Quentin Libois, Liviu Ivanescu, Jean-Pierre Blanchet, Hannes Schulz, Heiko Bozem, W. Richard Leaitch, Julia Burkart, Jonathan P. D. Abbatt, Andreas B. Herber, Amir A. Aliabadi, and Éric Girard
Atmos. Chem. Phys., 16, 15689–15707, https://doi.org/10.5194/acp-16-15689-2016, https://doi.org/10.5194/acp-16-15689-2016, 2016
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The first airborne measurements performed with the FIRR are presented. Vertical profiles of upwelling spectral radiance in the far-infrared are measured in the Arctic atmosphere for the first time. They show the impact of the temperature inversion on the radiative budget of the atmosphere, especially in the far-infrared. The presence of ice clouds also significantly alters the far-infrared budget, highlighting the critical interplay between water vapour and clouds in this very dry region.
Xuan Wang, Colette L. Heald, Arthur J. Sedlacek, Suzane S. de Sá, Scot T. Martin, M. Lizabeth Alexander, Thomas B. Watson, Allison C. Aiken, Stephen R. Springston, and Paulo Artaxo
Atmos. Chem. Phys., 16, 12733–12752, https://doi.org/10.5194/acp-16-12733-2016, https://doi.org/10.5194/acp-16-12733-2016, 2016
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We describe a new approach to estimate the absorption of brown carbon (BrC) from multiple-wavelength absorption measurements. By applying this method to column and surface observations globally, we find that BrC contributes up to 40 % of the absorption measured at 440 nm. The analysis of two surface sites also suggests that BrC absorptivity decreases with photochemical aging in biomass burning plumes, but not in typical urban conditions.
W. Richard Leaitch, Alexei Korolev, Amir A. Aliabadi, Julia Burkart, Megan D. Willis, Jonathan P. D. Abbatt, Heiko Bozem, Peter Hoor, Franziska Köllner, Johannes Schneider, Andreas Herber, Christian Konrad, and Ralf Brauner
Atmos. Chem. Phys., 16, 11107–11124, https://doi.org/10.5194/acp-16-11107-2016, https://doi.org/10.5194/acp-16-11107-2016, 2016
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Thought to be mostly unimportant for summertime Arctic liquid-water clouds, airborne observations show that atmospheric aerosol particles 50 nm in diameter or smaller and most likely from natural sources are often involved in cloud formation in the pristine Arctic summer. The result expands the reference for aerosol forcing of climate. Further, for extremely low droplet concentrations, no evidence is found for a connection between cloud liquid water and aerosol particle concentrations.
Amir A. Aliabadi, Jennie L. Thomas, Andreas B. Herber, Ralf M. Staebler, W. Richard Leaitch, Hannes Schulz, Kathy S. Law, Louis Marelle, Julia Burkart, Megan D. Willis, Heiko Bozem, Peter M. Hoor, Franziska Köllner, Johannes Schneider, Maurice Levasseur, and Jonathan P. D. Abbatt
Atmos. Chem. Phys., 16, 7899–7916, https://doi.org/10.5194/acp-16-7899-2016, https://doi.org/10.5194/acp-16-7899-2016, 2016
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For the first time, ship emissions of an ice-breaker, the Amundsen, is characterized while breaking ice in the Canadian Arctic using the plume intercepts by the Polar 6 aircraft. The study is novel, estimating lower plume expansion rates over the stable Arctic marine boundary layer and different emissions factors for oxides of nitrogen, black carbon, and carbon monoxide, compared to plume intercept studies in mid latitudes. These results can inform policy making and emission inventory datasets.
Alex K. Y. Lee, Jonathan P. D. Abbatt, W. Richard Leaitch, Shao-Meng Li, Steve J. Sjostedt, Jeremy J. B. Wentzell, John Liggio, and Anne Marie Macdonald
Atmos. Chem. Phys., 16, 6721–6733, https://doi.org/10.5194/acp-16-6721-2016, https://doi.org/10.5194/acp-16-6721-2016, 2016
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Substantial biogenic secondary organic aerosol (BSOA) formation was investigated in a coniferous forest mountain region in Whistler, British Columbia. A largely biogenic aerosol growth episode was observed, providing a unique opportunity to investigate BSOA formation chemistry in a forested environment. In particular, our observations provide insights into the relative importance of different oxidation mechanisms between day and night.
Betty Croft, Randall V. Martin, W. Richard Leaitch, Peter Tunved, Thomas J. Breider, Stephen D. D'Andrea, and Jeffrey R. Pierce
Atmos. Chem. Phys., 16, 3665–3682, https://doi.org/10.5194/acp-16-3665-2016, https://doi.org/10.5194/acp-16-3665-2016, 2016
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Measurements at high-Arctic sites show a strong annual cycle in atmospheric particle number and size. Previous studies identified poor scientific understanding related to global model representation of Arctic particle number and size, limiting ability to simulate this environment. Here we evaluate state-of-science ability to simulate Arctic particles using GEOS-Chem-TOMAS model, documenting key roles and interconnections of particle formation, cloud-related processes and remaining uncertainties.
S. Gagné, L. P. MacDonald, W. R. Leaitch, and J. R. Pierce
Atmos. Meas. Tech., 9, 619–630, https://doi.org/10.5194/amt-9-619-2016, https://doi.org/10.5194/amt-9-619-2016, 2016
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Measurements of clouds with an aircraft are essential to understand how clouds form and how they affect the Earth's climate. These measurements are used in climate models to help predict how our climate might develop in the next century. Aircraft measurements are, however, difficult for modellers to interpret because the way they were acquired and analyzed varies from one team of scientists to the next. We present a software platform for scientists to share and compare their analysis tools.
L. Kleinman, C. Kuang, A. Sedlacek, G. Senum, S. Springston, J. Wang, Q. Zhang, J. Jayne, J. Fast, J. Hubbe, J. Shilling, and R. Zaveri
Atmos. Chem. Phys., 16, 1729–1746, https://doi.org/10.5194/acp-16-1729-2016, https://doi.org/10.5194/acp-16-1729-2016, 2016
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Atmospheric measurements of total organic aerosol (OA) and tracers of anthropogenic and biogenic emissions are used to quantify synergistic effects (A–B interactions) between two classes of precursors in the formation of OA. Regressions are consistent with the Sacramento plume composed mainly of modern carbon, and OA correlating best with an anthropogenic tracer. It is found that meteorological conditions during a pollution episode can mimic effects of A–B interactions.
R. H. Mason, M. Si, C. Chou, V. E. Irish, R. Dickie, P. Elizondo, R. Wong, M. Brintnell, M. Elsasser, W. M. Lassar, K. M. Pierce, W. R. Leaitch, A. M. MacDonald, A. Platt, D. Toom-Sauntry, R. Sarda-Estève, C. L. Schiller, K. J. Suski, T. C. J. Hill, J. P. D. Abbatt, J. A. Huffman, P. J. DeMott, and A. K. Bertram
Atmos. Chem. Phys., 16, 1637–1651, https://doi.org/10.5194/acp-16-1637-2016, https://doi.org/10.5194/acp-16-1637-2016, 2016
L. Xu, L. R. Williams, D. E. Young, J. D. Allan, H. Coe, P. Massoli, E. Fortner, P. Chhabra, S. Herndon, W. A. Brooks, J. T. Jayne, D. R. Worsnop, A. C. Aiken, S. Liu, K. Gorkowski, M. K. Dubey, Z. L. Fleming, S. Visser, A. S. H. Prévôt, and N. L. Ng
Atmos. Chem. Phys., 16, 1139–1160, https://doi.org/10.5194/acp-16-1139-2016, https://doi.org/10.5194/acp-16-1139-2016, 2016
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We investigate the spatial distribution of submicron aerosol in the greater London area as part of the Clean Air for London (ClearfLo) project in winter 2012. Although the concentrations of organic aerosol (OA) are similar between a rural and an urban site, the OA sources are different. We also examine the volatility of submicron aerosol at the rural site and find that the non-volatile organics have similar sources or have undergone similar chemical processing as refractory black carbon.
S. D. D'Andrea, J. Y. Ng, J. K. Kodros, S. A. Atwood, M. J. Wheeler, A. M. Macdonald, W. R. Leaitch, and J. R. Pierce
Atmos. Chem. Phys., 16, 383–396, https://doi.org/10.5194/acp-16-383-2016, https://doi.org/10.5194/acp-16-383-2016, 2016
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We evaluate aerosol size distributions predicted by GEOS-Chem-TOMAS using measurements from the peak of Whistler Mountain. We improve model-measurement comparisons of aerosol number, size, and composition during periods of free-tropospheric and boundary-layer influence by developing simple filtering techniques, and determine the influence of Asian anthropogenic and biomass burning emissions. The low-cost filtering techniques and source apportionment methods can be used for other mountain sites.
F. Yu, G. Luo, S. C. Pryor, P. R. Pillai, S. H. Lee, J. Ortega, J. J. Schwab, A. G. Hallar, W. R. Leaitch, V. P. Aneja, J. N. Smith, J. T. Walker, O. Hogrefe, and K. L. Demerjian
Atmos. Chem. Phys., 15, 13993–14003, https://doi.org/10.5194/acp-15-13993-2015, https://doi.org/10.5194/acp-15-13993-2015, 2015
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The role of low-volatility organics in new particle formation (NPF) in the atmosphere is assessed. An empirical formulation in which formation rate is a function of the concentrations of sulfuric acid and low-volatility organics significantly overpredicts NPF in the summer.
Two different schemes predict quite different nucleation rates (including their spatial patterns), concentrations of cloud condensation nuclei, and aerosol first indirect radiative forcing in North America.
R. H. Mason, M. Si, J. Li, C. Chou, R. Dickie, D. Toom-Sauntry, C. Pöhlker, J. D. Yakobi-Hancock, L. A. Ladino, K. Jones, W. R. Leaitch, C. L. Schiller, J. P. D. Abbatt, J. A. Huffman, and A. K. Bertram
Atmos. Chem. Phys., 15, 12547–12566, https://doi.org/10.5194/acp-15-12547-2015, https://doi.org/10.5194/acp-15-12547-2015, 2015
E. Jung, B. A. Albrecht, H. H. Jonsson, Y.-C. Chen, J. H. Seinfeld, A. Sorooshian, A. R. Metcalf, S. Song, M. Fang, and L. M. Russell
Atmos. Chem. Phys., 15, 5645–5658, https://doi.org/10.5194/acp-15-5645-2015, https://doi.org/10.5194/acp-15-5645-2015, 2015
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To study the effect of giant cloud condensation nuclei (GCCN) on precipitation processes in stratocumulus clouds, 1-10 µm diameter salt particles were released from an aircraft while flying near the cloud top off the central coast of California. The analyses suggest that GCCN result in a four-fold increase in the cloud base rainfall rate and depletion of the cloud water due to rainout.
J. C. Schroder, S. J. Hanna, R. L. Modini, A. L. Corrigan, S. M. Kreidenwies, A. M. Macdonald, K. J. Noone, L. M. Russell, W. R. Leaitch, and A. K. Bertram
Atmos. Chem. Phys., 15, 1367–1383, https://doi.org/10.5194/acp-15-1367-2015, https://doi.org/10.5194/acp-15-1367-2015, 2015
S. M. Burrows, O. Ogunro, A. A. Frossard, L. M. Russell, P. J. Rasch, and S. M. Elliott
Atmos. Chem. Phys., 14, 13601–13629, https://doi.org/10.5194/acp-14-13601-2014, https://doi.org/10.5194/acp-14-13601-2014, 2014
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The air over the ocean is full of sea spray particles ejected by bubbles that burst in the wake of breaking waves. The smallest of such particles, less than a micrometer in diameter, include organic matter derived from ocean biota. This paper introduces a method to calculate the chemical composition of spray particles. Ocean organic matter is divided into several classes using a global model. Basic chemistry relationships predict the amount of organic material in emitted spray.
J. D. Yakobi-Hancock, L. A. Ladino, A. K. Bertram, J. A. Huffman, K. Jones, W. R. Leaitch, R. H. Mason, C. L. Schiller, D. Toom-Sauntry, J. P. S. Wong, and J. P. D. Abbatt
Atmos. Chem. Phys., 14, 12307–12317, https://doi.org/10.5194/acp-14-12307-2014, https://doi.org/10.5194/acp-14-12307-2014, 2014
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As one aspect of the NETwork on Climate and Aerosols: addressing key uncertainties in Remote Canadian Environments, measurements of the cloud condensation nucleation properties of 50 nm and 100 nm aerosol particles were conducted at Ucluelet on the west coast of Vancouver Island in August 2013. The most efficient cloud condensation nuclei arose when the organic to sulfate ratio of the aerosol was lowest and when winds arrived from the west after transport through the marine boundary layer.
K. Tsigaridis, N. Daskalakis, M. Kanakidou, P. J. Adams, P. Artaxo, R. Bahadur, Y. Balkanski, S. E. Bauer, N. Bellouin, A. Benedetti, T. Bergman, T. K. Berntsen, J. P. Beukes, H. Bian, K. S. Carslaw, M. Chin, G. Curci, T. Diehl, R. C. Easter, S. J. Ghan, S. L. Gong, A. Hodzic, C. R. Hoyle, T. Iversen, S. Jathar, J. L. Jimenez, J. W. Kaiser, A. Kirkevåg, D. Koch, H. Kokkola, Y. H Lee, G. Lin, X. Liu, G. Luo, X. Ma, G. W. Mann, N. Mihalopoulos, J.-J. Morcrette, J.-F. Müller, G. Myhre, S. Myriokefalitakis, N. L. Ng, D. O'Donnell, J. E. Penner, L. Pozzoli, K. J. Pringle, L. M. Russell, M. Schulz, J. Sciare, Ø. Seland, D. T. Shindell, S. Sillman, R. B. Skeie, D. Spracklen, T. Stavrakou, S. D. Steenrod, T. Takemura, P. Tiitta, S. Tilmes, H. Tost, T. van Noije, P. G. van Zyl, K. von Salzen, F. Yu, Z. Wang, Z. Wang, R. A. Zaveri, H. Zhang, K. Zhang, Q. Zhang, and X. Zhang
Atmos. Chem. Phys., 14, 10845–10895, https://doi.org/10.5194/acp-14-10845-2014, https://doi.org/10.5194/acp-14-10845-2014, 2014
J. D. Fast, J. Allan, R. Bahreini, J. Craven, L. Emmons, R. Ferrare, P. L. Hayes, A. Hodzic, J. Holloway, C. Hostetler, J. L. Jimenez, H. Jonsson, S. Liu, Y. Liu, A. Metcalf, A. Middlebrook, J. Nowak, M. Pekour, A. Perring, L. Russell, A. Sedlacek, J. Seinfeld, A. Setyan, J. Shilling, M. Shrivastava, S. Springston, C. Song, R. Subramanian, J. W. Taylor, V. Vinoj, Q. Yang, R. A. Zaveri, and Q. Zhang
Atmos. Chem. Phys., 14, 10013–10060, https://doi.org/10.5194/acp-14-10013-2014, https://doi.org/10.5194/acp-14-10013-2014, 2014
J. R. Pierce, D. M. Westervelt, S. A. Atwood, E. A. Barnes, and W. R. Leaitch
Atmos. Chem. Phys., 14, 8647–8663, https://doi.org/10.5194/acp-14-8647-2014, https://doi.org/10.5194/acp-14-8647-2014, 2014
S. Gilardoni, P. Massoli, L. Giulianelli, M. Rinaldi, M. Paglione, F. Pollini, C. Lanconelli, V. Poluzzi, S. Carbone, R. Hillamo, L. M. Russell, M. C. Facchini, and S. Fuzzi
Atmos. Chem. Phys., 14, 6967–6981, https://doi.org/10.5194/acp-14-6967-2014, https://doi.org/10.5194/acp-14-6967-2014, 2014
J. Kangasluoma, C. Kuang, D. Wimmer, M. P. Rissanen, K. Lehtipalo, M. Ehn, D. R. Worsnop, J. Wang, M. Kulmala, and T. Petäjä
Atmos. Meas. Tech., 7, 689–700, https://doi.org/10.5194/amt-7-689-2014, https://doi.org/10.5194/amt-7-689-2014, 2014
A. Steffen, J. Bottenheim, A. Cole, R. Ebinghaus, G. Lawson, and W. R. Leaitch
Atmos. Chem. Phys., 14, 2219–2231, https://doi.org/10.5194/acp-14-2219-2014, https://doi.org/10.5194/acp-14-2219-2014, 2014
B. H. Kahn, F. W. Irion, V. T. Dang, E. M. Manning, S. L. Nasiri, C. M. Naud, J. M. Blaisdell, M. M. Schreier, Q. Yue, K. W. Bowman, E. J. Fetzer, G. C. Hulley, K. N. Liou, D. Lubin, S. C. Ou, J. Susskind, Y. Takano, B. Tian, and J. R. Worden
Atmos. Chem. Phys., 14, 399–426, https://doi.org/10.5194/acp-14-399-2014, https://doi.org/10.5194/acp-14-399-2014, 2014
A. L. Corrigan, L. M. Russell, S. Takahama, M. Äijälä, M. Ehn, H. Junninen, J. Rinne, T. Petäjä, M. Kulmala, A. L. Vogel, T. Hoffmann, C. J. Ebben, F. M. Geiger, P. Chhabra, J. H. Seinfeld, D. R. Worsnop, W. Song, J. Auld, and J. Williams
Atmos. Chem. Phys., 13, 12233–12256, https://doi.org/10.5194/acp-13-12233-2013, https://doi.org/10.5194/acp-13-12233-2013, 2013
S. D. D'Andrea, S. A. K. Häkkinen, D. M. Westervelt, C. Kuang, E. J. T. Levin, V. P. Kanawade, W. R. Leaitch, D. V. Spracklen, I. Riipinen, and J. R. Pierce
Atmos. Chem. Phys., 13, 11519–11534, https://doi.org/10.5194/acp-13-11519-2013, https://doi.org/10.5194/acp-13-11519-2013, 2013
A. L. Vogel, M. Äijälä, A. L. Corrigan, H. Junninen, M. Ehn, T. Petäjä, D. R. Worsnop, M. Kulmala, L. M. Russell, J. Williams, and T. Hoffmann
Atmos. Chem. Phys., 13, 10933–10950, https://doi.org/10.5194/acp-13-10933-2013, https://doi.org/10.5194/acp-13-10933-2013, 2013
A. Wonaschütz, M. Coggon, A. Sorooshian, R. Modini, A. A. Frossard, L. Ahlm, J. Mülmenstädt, G. C. Roberts, L. M. Russell, S. Dey, F. J. Brechtel, and J. H. Seinfeld
Atmos. Chem. Phys., 13, 9819–9835, https://doi.org/10.5194/acp-13-9819-2013, https://doi.org/10.5194/acp-13-9819-2013, 2013
E. Kostenidou, C. Kaltsonoudis, M. Tsiflikiotou, E. Louvaris, L. M. Russell, and S. N. Pandis
Atmos. Chem. Phys., 13, 8797–8811, https://doi.org/10.5194/acp-13-8797-2013, https://doi.org/10.5194/acp-13-8797-2013, 2013
M. D. Gibson, J. R. Pierce, D. Waugh, J. S. Kuchta, L. Chisholm, T. J. Duck, J. T. Hopper, S. Beauchamp, G. H. King, J. E. Franklin, W. R. Leaitch, A. J. Wheeler, Z. Li, G. A. Gagnon, and P. I. Palmer
Atmos. Chem. Phys., 13, 7199–7213, https://doi.org/10.5194/acp-13-7199-2013, https://doi.org/10.5194/acp-13-7199-2013, 2013
J. Wang, R. L. McGraw, and C. Kuang
Atmos. Chem. Phys., 13, 6523–6531, https://doi.org/10.5194/acp-13-6523-2013, https://doi.org/10.5194/acp-13-6523-2013, 2013
B. Ervens, Y. Wang, J. Eagar, W. R. Leaitch, A. M. Macdonald, K. T. Valsaraj, and P. Herckes
Atmos. Chem. Phys., 13, 5117–5135, https://doi.org/10.5194/acp-13-5117-2013, https://doi.org/10.5194/acp-13-5117-2013, 2013
L. Ahlm, K. M. Shakya, L. M. Russell, J. C. Schroder, J. P. S. Wong, S. J. Sjostedt, K. L. Hayden, J. Liggio, J. J. B. Wentzell, H. A. Wiebe, C. Mihele, W. R. Leaitch, and A. M. Macdonald
Atmos. Chem. Phys., 13, 3393–3407, https://doi.org/10.5194/acp-13-3393-2013, https://doi.org/10.5194/acp-13-3393-2013, 2013
Related subject area
Subject: Aerosols | Research Activity: Field Measurements | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Molecular characterization of organic aerosols in urban and forested areas of Paris using high-resolution mass spectrometry
Measurement report: Wintertime aerosol characterization at an urban traffic site in Helsinki, Finland
Source apportionment and ecotoxicity of PM2.5 pollution events in a major Southern Hemisphere megacity: influence of a biofuel-impacted fleet and biomass burning
Marine organic aerosol at Mace Head: effects from phytoplankton and source region variability
Measurement report: Sources and meteorology influencing highly time-resolved PM2.5 trace elements at three urban sites in the extremely polluted Indo-Gangetic Plain in India
Formation of highly absorptive secondary brown carbon through nighttime multiphase chemistry of biomass burning emissions
Measurement report: Vertically resolved atmospheric properties observed over the Southern Great Plains with the ArcticShark uncrewed aerial system
Non-biogenic sources are an important but overlooked contributor to aerosol isoprene-derived organosulfates during winter in northern China
The critical role of aqueous-phase processes in aromatic-derived nitrogen-containing organic aerosol formation in cities with different energy consumption patterns
Characterization of atmospheric water-soluble brown carbon in the Athabasca oil sands region, Canada
Sensitivity of aerosol and cloud properties to coupling strength of marine boundary layer clouds over the northwest Atlantic
Measurement Report: Molecular composition, sources, and evolution of atmospheric organic aerosols in a basin city in China
Burning conditions and transportation pathways determine biomass-burning aerosol properties in the Ascension Island marine boundary layer
Observations of high-time-resolution and size-resolved aerosol chemical composition and microphysics in the central Arctic: implications for climate-relevant particle properties
Measurement report: Brown carbon aerosol in rural Germany – sources, chemistry, and diurnal variations
Particle flux-gradient relationships in the high Arctic: Emission and deposition patterns across three surface types
Multiple eco-regions contribute to the seasonal cycle of Antarctic aerosol size distributions
Seasonal investigation of ultrafine-particle organic composition in an eastern Amazonian rainforest
Characterizing lead-rich particles in Beijing's atmosphere following coal-to-gas conversion: Insights from single particle aerosol mass spectrometry
High-resolution analyses of concentrations and sizes of refractory black carbon particles deposited in northwestern Greenland over the past 350 years – Part 2: Seasonal and temporal trends in refractory black carbon originated from fossil fuel combustion and biomass burning
Direct measurement of N2O5 heterogeneous uptake coefficients on atmospheric aerosols in southwestern China and evaluation of current parameterizations
Measurement report: Per- and polyfluoroalkyl substances (PFAS) in particulate matter (PM10) from activated sludge aeration
Significant role of biomass burning in heavy haze formation in Nanjing, a megacity in China: molecular-level insights from intensive PM2.5 sampling on winter hazy days
Widespread trace bromine and iodine in remote tropospheric non-sea-salt aerosols
Significant contributions of biomass burning to PM2.5-bound aromatic compounds: insights from field observations and quantum chemical calculations
A 60-year atmospheric nitrate isotope record from a Southeast Greenland ice core with minimal post-depositional alteration
Iron isotopes reveal significant aerosol dissolution over the Pacific Ocean
Formation and chemical evolution of secondary organic aerosol in two different environments: a dual-chamber study
Enrichment of organic nitrogen in fog residuals observed in the Italian Po Valley
Technical note: Quantified organic aerosol subsaturated hygroscopicity by a simple optical scatter monitor system through field measurements
Measurement report: Oxidation potential of water-soluble aerosol components in the south and north of Beijing
Enhanced daytime secondary aerosol formation driven by gas–particle partitioning in downwind urban plumes
Technical note: Reconstructing surface missing aerosol elemental carbon data in long-term series with ensemble learning
Understanding the mechanism and importance of brown carbon bleaching across the visible spectrum in biomass burning plumes from the WE-CAN campaign
Influence of terrestrial and marine air mass on the constituents and intermixing of bioaerosols over a coastal atmosphere
A multi-site passive approach to studying the emissions and evolution of smoke from prescribed fires
The annual cycle and sources of relevant aerosol precursor vapors in the central Arctic during the MOSAiC expedition
Enhanced emission of intermediate/semi-volatile organic matters in both gas and particle phases from ship exhausts with low-sulfur fuels
Advances in characterization of black carbon particles and their associated coatings using the soot particle aerosol mass spectrometer in Singapore, a complex city environment
Measurement report: Crustal materials play an increasing role in elevating particle pH: Insights from 12-year records in a typical inland city of China
African dust transported to Barbados in the Wintertime Lacks Indicators of Chemical Aging
Opinion: How will advances in aerosol science inform our understanding of the health impacts of outdoor particulate pollution?
Machine Learning Assisted Chemical Characterization and Optical Properties of Atmospheric Brown Carbon in Nanjing, China
Measurement report: Intra-annual variability of black carbon and brown carbon and their interrelation with meteorological conditions over Gangtok, Sikkim
Long-range transport of air pollutants increases the concentration of hazardous components of PM2.5 in northern South America
Dominant influence of biomass combustion and cross-border transport on nitrogen-containing organic compound levels in the southeastern Tibetan Plateau
Impacts of elevated anthropogenic emissions on physicochemical characteristics of black-carbon-containing particles over the Tibetan Plateau
Online characterization of primary and secondary emissions of particulate matter and acidic molecules from a modern fleet of city buses
Atmospheric evolution of environmentally persistent free radicals in the rural North China Plain: effects on water solubility and PM2.5 oxidative potential
Measurement report: Characterization of Aerosol Hygroscopicity over Southeast Asia during the NASA CAMP2Ex Campaign
Diana L. Pereira, Chiara Giorio, Aline Gratien, Alexander Zherebker, Gael Noyalet, Servanne Chevaillier, Stéphanie Alage, Elie Almarj, Antonin Bergé, Thomas Bertin, Mathieu Cazaunau, Patrice Coll, Ludovico Di Antonio, Sergio Harb, Johannes Heuser, Cécile Gaimoz, Oscar Guillemant, Brigitte Language, Olivier Lauret, Camilo Macias, Franck Maisonneuve, Bénédicte Picquet-Varrault, Raquel Torres, Sylvain Triquet, Pascal Zapf, Lelia Hawkins, Drew Pronovost, Sydney Riley, Pierre-Marie Flaud, Emilie Perraudin, Pauline Pouyes, Eric Villenave, Alexandre Albinet, Olivier Favez, Robin Aujay-Plouzeau, Vincent Michoud, Christopher Cantrell, Manuela Cirtog, Claudia Di Biagio, Jean-François Doussin, and Paola Formenti
Atmos. Chem. Phys., 25, 4885–4905, https://doi.org/10.5194/acp-25-4885-2025, https://doi.org/10.5194/acp-25-4885-2025, 2025
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In order to study aerosols in environments influenced by anthropogenic and biogenic emissions, we performed analyses of samples collected during the ACROSS (Atmospheric Chemistry Of the Suburban Forest) campaign in summer 2022 in the greater Paris area. After analysis of the chemical composition by means of total carbon determination and high-resolution mass spectrometry, this work highlights the influence of anthropogenic inputs on the chemical composition of both urban and forested areas.
Kimmo Teinilä, Sanna Saarikoski, Henna Lintusaari, Teemu Lepistö, Petteri Marjanen, Minna Aurela, Heidi Hellén, Toni Tykkä, Markus Lampimäki, Janne Lampilahti, Luis Barreira, Timo Mäkelä, Leena Kangas, Juha Hatakka, Sami Harni, Joel Kuula, Jarkko V. Niemi, Harri Portin, Jaakko Yli-Ojanperä, Ville Niemelä, Milja Jäppi, Katrianne Lehtipalo, Joonas Vanhanen, Liisa Pirjola, Hanna E. Manninen, Tuukka Petäjä, Topi Rönkkö, and Hilkka Timonen
Atmos. Chem. Phys., 25, 4907–4928, https://doi.org/10.5194/acp-25-4907-2025, https://doi.org/10.5194/acp-25-4907-2025, 2025
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Physical and chemical properties of particulate matter and concentrations of trace gases were measured in a street canyon in Helsinki, Finland, and an urban background site in January–February 2022 to investigate the effect of wintertime conditions on pollutants. State-of-the-art instruments and a mobile laboratory were used, and the measurement data were analysed further with modelling tools like positive matrix factorization and the Pollution Detection Algorithm.
Guilherme Martins Pereira, Leonardo Yoshiaki Kamigauti, Rubens Fabio Pereira, Djacinto Monteiro dos Santos, Thayná da Silva Santos, José Vinicius Martins, Célia Alves, Cátia Gonçalves, Ismael Casotti Rienda, Nora Kováts, Thiago Nogueira, Luciana Rizzo, Paulo Artaxo, Regina Maura de Miranda, Marcia Akemi Yamasoe, Edmilson Dias de Freitas, Pérola de Castro Vasconcellos, and Maria de Fatima Andrade
Atmos. Chem. Phys., 25, 4587–4616, https://doi.org/10.5194/acp-25-4587-2025, https://doi.org/10.5194/acp-25-4587-2025, 2025
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The chemical composition of fine particulate matter was studied in the megacity of São Paulo (Brazil) during a polluted period. Vehicular-related sources remain relevant; however, a high contribution of biomass burning was observed and correlated with sample ecotoxicity. Emerging biomass burning sources, such as forest fires and sugarcane-bagasse-based power plants, highlight the need for additional control measures alongside stricter rules concerning vehicular emissions.
Emmanuel Chevassus, Kirsten N. Fossum, Darius Ceburnis, Lu Lei, Chunshui Lin, Wei Xu, Colin O'Dowd, and Jurgita Ovadnevaite
Atmos. Chem. Phys., 25, 4107–4129, https://doi.org/10.5194/acp-25-4107-2025, https://doi.org/10.5194/acp-25-4107-2025, 2025
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This study presents the first source apportionment of organic aerosol at Mace Head via high-resolution mass spectrometry. Introducing transfer entropy as a novel method reveals that aged organic aerosol originates from both open-ocean ozonolysis and local peat-burning oxidation. Methanesulfonic acid and organic sea spray both mirror phytoplankton activity, with the former closely tied to coccolithophore blooms and the latter linked to diatoms, chlorophytes, and cyanobacteria.
Ashutosh K. Shukla, Sachchida N. Tripathi, Shamitaksha Talukdar, Vishnu Murari, Sreenivas Gaddamidi, Manousos-Ioannis Manousakas, Vipul Lalchandani, Kuldeep Dixit, Vinayak M. Ruge, Peeyush Khare, Mayank Kumar, Vikram Singh, Neeraj Rastogi, Suresh Tiwari, Atul K. Srivastava, Dilip Ganguly, Kaspar Rudolf Daellenbach, and André S. H. Prévôt
Atmos. Chem. Phys., 25, 3765–3784, https://doi.org/10.5194/acp-25-3765-2025, https://doi.org/10.5194/acp-25-3765-2025, 2025
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Our study delves into the elemental composition of aerosols at three sites across the Indo-Gangetic Plain (IGP), revealing distinct patterns during pollution episodes. We found significant increases in chlorine (Cl)-rich and solid fuel combustion (SFC) sources, indicating dynamic emission sources, agricultural burning impacts, and meteorological influences. Surges in Cl-rich particles during cold periods highlight their role in particle growth under high-relative-humidity conditions.
Ye Kuang, Biao Luo, Shan Huang, Junwen Liu, Weiwei Hu, Yuwen Peng, Duohong Chen, Dingli Yue, Wanyun Xu, Bin Yuan, and Min Shao
Atmos. Chem. Phys., 25, 3737–3752, https://doi.org/10.5194/acp-25-3737-2025, https://doi.org/10.5194/acp-25-3737-2025, 2025
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This research reveals the potential importance of nighttime NO3 radical chemistry and aerosol water in the rapid formation of secondary brown carbon from diluted biomass burning emissions. The findings enhance our understanding of nighttime biomass burning evolution and its implications for climate and regional air quality, especially regarding interactions with background aerosol water and water-rich fogs and clouds.
Fan Mei, Qi Zhang, Damao Zhang, Jerome D. Fast, Gourihar Kulkarni, Mikhail S. Pekour, Christopher R. Niedek, Susanne Glienke, Israel Silber, Beat Schmid, Jason M. Tomlinson, Hardeep S. Mehta, Xena Mansoura, Zezhen Cheng, Gregory W. Vandergrift, Nurun Nahar Lata, Swarup China, and Zihua Zhu
Atmos. Chem. Phys., 25, 3425–3444, https://doi.org/10.5194/acp-25-3425-2025, https://doi.org/10.5194/acp-25-3425-2025, 2025
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This study highlights the unique capability of the ArcticShark, an uncrewed aerial system, in measuring vertically resolved atmospheric properties. Data from 32 research flights in 2023 reveal seasonal patterns and correlations with conventional measurements. The consistency and complementarity of in situ and remote sensing methods are highlighted. The study demonstrates the ArcticShark’s versatility in bridging data gaps and improving the understanding of vertical atmospheric structures.
Ting Yang, Yu Xu, Yu-Chen Wang, Yi-Jia Ma, Hong-Wei Xiao, Hao Xiao, and Hua-Yun Xiao
Atmos. Chem. Phys., 25, 2967–2978, https://doi.org/10.5194/acp-25-2967-2025, https://doi.org/10.5194/acp-25-2967-2025, 2025
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Previous measurement–model comparisons of atmospheric isoprene levels showed a significant unidentified source of isoprene in some northern Chinese cities during winter. Here, the first combination of large-scale observations and field combustion experiments provides novel insights into biomass burning emissions as a significant source of isoprene-derived organosulfates during winter in northern cities of China.
Yi-Jia Ma, Yu Xu, Ting Yang, Lin Gui, Hong-Wei Xiao, Hao Xiao, and Hua-Yun Xiao
Atmos. Chem. Phys., 25, 2763–2780, https://doi.org/10.5194/acp-25-2763-2025, https://doi.org/10.5194/acp-25-2763-2025, 2025
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The abundance, potential precursors, and main formation mechanisms of nitrogen-containing organic compounds (NOCs) in PM2.5 during winter were compared among cities with different energy consumption patterns. The aerosol NOC pollution during winter in China is closely associated with the intensity of precursor emissions and the aqueous-phase processes. Our results highlight the importance of emission reduction strategies in controlling aerosol NOCs pollution during winter in China.
Dane Blanchard, Mark Gordon, Duc Huy Dang, Paul Andrew Makar, and Julian Aherne
Atmos. Chem. Phys., 25, 2423–2442, https://doi.org/10.5194/acp-25-2423-2025, https://doi.org/10.5194/acp-25-2423-2025, 2025
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This study offers the first known evaluation of water-soluble brown carbon aerosols in the Athabasca oil sands region (AOSR), Canada. Fluorescence spectroscopy analysis of aerosol samples from five regional sites (collected during the summer of 2021) identified oil sands operations as a measurable brown carbon source. Industrial aerosol emissions were unlikely to impact regional radiative forcing. These findings show that fluorescence spectroscopy can be used to monitor brown carbon in the AOSR.
Kira Zeider, Kayla McCauley, Sanja Dmitrovic, Leong Wai Siu, Yonghoon Choi, Ewan C. Crosbie, Joshua P. DiGangi, Glenn S. Diskin, Simon Kirschler, John B. Nowak, Michael A. Shook, Kenneth L. Thornhill, Christiane Voigt, Edward L. Winstead, Luke D. Ziemba, Paquita Zuidema, and Armin Sorooshian
Atmos. Chem. Phys., 25, 2407–2422, https://doi.org/10.5194/acp-25-2407-2025, https://doi.org/10.5194/acp-25-2407-2025, 2025
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In situ aircraft data collected over the northwest Atlantic Ocean are utilized to compare aerosol conditions and turbulence between near-surface and below-cloud-base altitudes for different regimes of coupling strength between those two levels, along with how cloud microphysical properties vary across those regimes. Stronger coupling yields more homogenous aerosol structure vertically along with higher cloud drop concentrations and sea salt influence in clouds.
Junke Zhang, Xinyi Fu, Chunying Chen, Yunfei Su, Siyu Liu, Luyao Chen, Yubao Chen, Gehui Wang, and Andre S. H. Prevot
EGUsphere, https://doi.org/10.5194/egusphere-2025-92, https://doi.org/10.5194/egusphere-2025-92, 2025
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The 125 organic aerosol (OA) compounds in PM2.5 in winter in Chengdu were measured at the molecular level. OA was dominated by fatty acids, phthalate esters, and anhydrosugars, and were deeply influenced by anthropogenic sources. As pollution worsens: secondary inorganic species and secondary organic carbon (OC) dominated the increase in PM2.5; fatty acids and anhydrosugars dominated the increase in OA; and the contribution of secondary formation and biomass burning to OC increased markedly.
Amie Dobracki, Ernie R. Lewis, Arthur J. Sedlacek III, Tyler Tatro, Maria A. Zawadowicz, and Paquita Zuidema
Atmos. Chem. Phys., 25, 2333–2363, https://doi.org/10.5194/acp-25-2333-2025, https://doi.org/10.5194/acp-25-2333-2025, 2025
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Biomass-burning aerosol is commonly present in the marine boundary layer over the southeast Atlantic Ocean between June and October. Our research indicates that burning conditions, aerosol transport pathways, and prolonged oxidation processes (heterogeneous and aqueous phases) determine the chemical, microphysical, and optical properties of the boundary layer aerosol. Notably, we find that the aerosol optical properties can be estimated from the chemical properties alone.
Benjamin Heutte, Nora Bergner, Hélène Angot, Jakob B. Pernov, Lubna Dada, Jessica A. Mirrielees, Ivo Beck, Andrea Baccarini, Matthew Boyer, Jessie M. Creamean, Kaspar R. Daellenbach, Imad El Haddad, Markus M. Frey, Silvia Henning, Tiia Laurila, Vaios Moschos, Tuukka Petäjä, Kerri A. Pratt, Lauriane L. J. Quéléver, Matthew D. Shupe, Paul Zieger, Tuija Jokinen, and Julia Schmale
Atmos. Chem. Phys., 25, 2207–2241, https://doi.org/10.5194/acp-25-2207-2025, https://doi.org/10.5194/acp-25-2207-2025, 2025
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Limited aerosol measurements in the central Arctic hinder our understanding of aerosol–climate interactions in the region. Our year-long observations of aerosol physicochemical properties during the MOSAiC expedition reveal strong seasonal variations in aerosol chemical composition, where the short-term variability is heavily affected by storms in the Arctic. Local wind-generated particles are shown to be an important source of cloud seeds, especially in autumn.
Feng Jiang, Harald Saathoff, Uzoamaka Ezenobi, Junwei Song, Hengheng Zhang, Linyu Gao, and Thomas Leisner
Atmos. Chem. Phys., 25, 1917–1930, https://doi.org/10.5194/acp-25-1917-2025, https://doi.org/10.5194/acp-25-1917-2025, 2025
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The chemical composition of brown carbon in the particle and gas phase was determined by mass spectrometry. BrC in the gas phase was mainly controlled by secondary formation and particle-to-gas partitioning. BrC in the particle phase was mainly from secondary formation. This work helps to get a better understanding of diurnal variations and the sources of brown carbon aerosol at a rural location in central Europe.
Theresa Mathes, Heather Guy, John Prytherch, Julia Kojoj, Ian Brooks, Sonja Murto, Paul Zieger, Birgit Wehner, Michael Tjernström, and Andreas Held
EGUsphere, https://doi.org/10.5194/egusphere-2025-183, https://doi.org/10.5194/egusphere-2025-183, 2025
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The Arctic is warming faster than the global average and aerosol-cloud-sea-ice interactions are crucial for studying its climate system. During the ARTofMELT Expedition 2023, particle and sensible heat fluxes were measured over multiple surfaces. Wide lead surfaces acted as particle sources with the strongest sensible heat fluxes, while closed ice surfaces acted as a particle sink. This study improves methods to measure these interactions, enhancing our understanding of Arctic climate processes.
James Brean, David C. S. Beddows, Eija Asmi, Aki Virkkula, Lauriane L. J. Quéléver, Mikko Sipilä, Floortje Van Den Heuvel, Thomas Lachlan-Cope, Anna Jones, Markus Frey, Angelo Lupi, Jiyeon Park, Young Jun Yoon, Rolf Weller, Giselle L. Marincovich, Gabriela C. Mulena, Roy M. Harrison, and Manuel Dall'Osto
Atmos. Chem. Phys., 25, 1145–1162, https://doi.org/10.5194/acp-25-1145-2025, https://doi.org/10.5194/acp-25-1145-2025, 2025
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Our results emphasise how understanding the geographical variation in surface types across the Antarctic is key to understanding secondary aerosol sources.
Adam E. Thomas, Hayley S. Glicker, Alex B. Guenther, Roger Seco, Oscar Vega Bustillos, Julio Tota, Rodrigo A. F. Souza, and James N. Smith
Atmos. Chem. Phys., 25, 959–977, https://doi.org/10.5194/acp-25-959-2025, https://doi.org/10.5194/acp-25-959-2025, 2025
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We present measurements of the organic composition of ultrafine particles collected from the eastern Amazon, an understudied region that is subjected to increasing human influence. We find that while isoprene chemistry is likely significant for ultrafine-particle growth throughout the year, compounds related to other sources, such as biological-spore emissions and biomass burning, exhibit striking seasonal differences, implying extensive variation in regional ultrafine-particle sources.
Xiufeng Lian, Yongjiang Xu, Fengxian Liu, Long Peng, Xiaodong Hu, Guigang Tang, Xu Dao, Hui Guo, Liwei Wang, Bo Huang, Chunlei Cheng, Lei Li, Guohua Zhang, Xinhui Bi, Xiaofei Wang, Zhen Zhou, and Mei Li
EGUsphere, https://doi.org/10.5194/egusphere-2024-3469, https://doi.org/10.5194/egusphere-2024-3469, 2025
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In this study, we analyzed the mixing state and atmospheric chemical processes of Pb-rich single particles in Beijing. Then, we focused on analyzing the differences in Pb-rich particles between the heating period and non-heating period, as well as the formation mechanism of lead nitrate after coal-to-gas conversion. Our results highlighted the improvement of coal-to-gas conversion on Pb in the particulate.
Kumiko Goto-Azuma, Yoshimi Ogawa-Tsukagawa, Kaori Fukuda, Koji Fujita, Motohiro Hirabayashi, Remi Dallmayr, Jun Ogata, Nobuhiro Moteki, Tatsuhiro Mori, Sho Ohata, Yutaka Kondo, Makoto Koike, Sumito Matoba, Moe Kadota, Akane Tsushima, Naoko Nagatsuka, and Teruo Aoki
Atmos. Chem. Phys., 25, 657–683, https://doi.org/10.5194/acp-25-657-2025, https://doi.org/10.5194/acp-25-657-2025, 2025
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Monthly ice core records spanning 350 years from Greenland show trends in refractory black carbon (rBC) concentrations and sizes. rBC levels have increased since the 1870s due to the inflow of anthropogenic rBC, with larger diameters than those from biomass burning (BB) rBC. High summer BB rBC peaks may reduce the ice sheet albedo, but BB rBC showed no increase until the early 2000s. These results are vital for validating aerosol and climate models.
Jiayin Li, Tianyu Zhai, Xiaorui Chen, Haichao Wang, Shuyang Xie, Shiyi Chen, Chunmeng Li, Huabin Dong, and Keding Lu
EGUsphere, https://doi.org/10.5194/egusphere-2024-3804, https://doi.org/10.5194/egusphere-2024-3804, 2025
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We directly measured the dinitrogen pentoxide (N2O5) uptake coefficient which critical impact the NOx fate and particulate nitrate formation in a typical highland city, Kunming, in China. We found the performance of current γ(N2O5) parameterizations showed deviations with the varying aerosol liquid water content (ALWC). Such differences would lead to biased estimation on particulate nitrate production potential. Our findings suggest the directions for future studies.
Jishnu Pandamkulangara Kizhakkethil, Zongbo Shi, Anna Bogush, and Ivan Kourtchev
EGUsphere, https://doi.org/10.5194/egusphere-2024-3952, https://doi.org/10.5194/egusphere-2024-3952, 2025
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Pollution with per- and polyfluoroalkyl substances (PFAS) received attention due to their environmental persistence and bioaccumulation. PM10 collected above a scaled-down activated sludge tank treating domestic sewage for a population >10,000 people in the UK were analysed for a range of short-, medium- and long-chain PFAS. Eight PFAS were detected in the PM10. Our results suggest that wastewater treatment processes i.e. activated sludge aeration could aerosolise PFAS into airborne PM.
Mingjie Kang, Mengying Bao, Wenhuai Song, Aduburexiati Abulimiti, Changliu Wu, Fang Cao, Sönke Szidat, and Yanlin Zhang
Atmos. Chem. Phys., 25, 73–91, https://doi.org/10.5194/acp-25-73-2025, https://doi.org/10.5194/acp-25-73-2025, 2025
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Reports on molecular-level knowledge of high-temporal-resolution particulate matter ≤2.5 µm in diameter (PM2.5) on hazy days are limited. We investigated various PM2.5 species and their sources. The results show biomass burning (BB) was the main source of organic carbon. Moreover, BB enhanced fungal spore emissions and secondary aerosol formation. The contribution of non-fossil sources increased with increasing haze pollution, suggesting BB may be an important driver of haze events in winter.
Gregory P. Schill, Karl D. Froyd, Daniel M. Murphy, Christina J. Williamson, Charles A. Brock, Tomás Sherwen, Mat J. Evans, Eric A. Ray, Eric C. Apel, Rebecca S. Hornbrook, Alan J. Hills, Jeff Peischl, Thomas B. Ryerson, Chelsea R. Thompson, Ilann Bourgeois, Donald R. Blake, Joshua P. DiGangi, and Glenn S. Diskin
Atmos. Chem. Phys., 25, 45–71, https://doi.org/10.5194/acp-25-45-2025, https://doi.org/10.5194/acp-25-45-2025, 2025
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Using single-particle mass spectrometry, we show that trace concentrations of bromine and iodine are ubiquitous in remote tropospheric aerosol and suggest that aerosols are an important part of the global reactive iodine budget. Comparisons to a global climate model with detailed iodine chemistry are favorable in the background atmosphere; however, the model cannot replicate our measurements near the ocean surface, in biomass burning plumes, and in the stratosphere.
Yanqin Ren, Zhenhai Wu, Fang Bi, Hong Li, Haijie Zhang, Junling Li, Rui Gao, Fangyun Long, Zhengyang Liu, Yuanyuan Ji, and Gehui Wang
EGUsphere, https://doi.org/10.5194/egusphere-2024-3678, https://doi.org/10.5194/egusphere-2024-3678, 2025
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The daily concentrations of Polycyclic aromatic hydrocarbons (PAHs), oxygenated PAHs (OPAHs), and nitrated phenols (NPs) in PM2.5 were all increased during the heating season. Biomass burning was identified to be the primary source of these aromatic compounds, particularly for PAHs. Phenol and nitrobenzene are two main primary precursors for 4NP, with phenol showing lower reaction barriers. P-Cresol was identified as the primary precursor for the formation of 4-methyl-5-nitrocatechol.
Zhao Wei, Shohei Hattori, Asuka Tsuruta, Zhuang Jiang, Sakiko Ishino, Koji Fujita, Sumito Matoba, Lei Geng, Alexis Lamothe, Ryu Uemura, Naohiro Yoshida, Joel Savarino, and Yoshinori Iizuka
EGUsphere, https://doi.org/10.5194/egusphere-2024-3937, https://doi.org/10.5194/egusphere-2024-3937, 2024
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Nitrate isotope records in ice cores reveal changes in NOₓ emissions, atmospheric acidity, and oxidation chemistry driven by human activity. However, nitrate in snow can be altered by UV-driven post-depositional processes, making snow accumulation rates critical for preserving these records. This study examines nitrate isotopes in an SE-Dome ice core, where high snow accumulation minimizes these effects, providing a reliable archive of atmospheric nitrogen cycling.
Capucine Camin, François Lacan, Catherine Pradoux, Marie Labatut, Anne Johansen, and James W. Murray
EGUsphere, https://doi.org/10.5194/egusphere-2024-3777, https://doi.org/10.5194/egusphere-2024-3777, 2024
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This manuscript presents the chemical composition of aerosols (> 1µm) over the Equatorial and Tropical Pacific Ocean, presenting the first measurements of iron isotopes in aerosols from this region. Iron concentrations and isotopes were determined using a Neptune MC-ICPMS. Our data analysis reveals that a significant portion of the aerosols undergo dissolution and removal during atmospheric transport. These findings contribute to original conclusions about the chemistry and physics of aerosols.
Andreas Aktypis, Dontavious J. Sippial, Christina N. Vasilakopoulou, Angeliki Matrali, Christos Kaltsonoudis, Andrea Simonati, Marco Paglione, Matteo Rinaldi, Stefano Decesari, and Spyros N. Pandis
Atmos. Chem. Phys., 24, 13769–13791, https://doi.org/10.5194/acp-24-13769-2024, https://doi.org/10.5194/acp-24-13769-2024, 2024
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A dual-chamber system was deployed in two different environments (Po Valley, Italy, and Pertouli forest, Greece) to study the potential of ambient air directly injected into the chambers, to form secondary organic aerosol (SOA). In the Po Valley, the system reacts rapidly, forming large amounts of SOA, while in Pertouli the SOA formation chemistry appears to have been practically terminated before the beginning of most experiments, so there is little additional SOA formation potential left.
Fredrik Mattsson, Almuth Neuberger, Liine Heikkinen, Yvette Gramlich, Marco Paglione, Matteo Rinaldi, Stefano Decesari, Paul Zieger, Ilona Riipinen, and Claudia Mohr
EGUsphere, https://doi.org/10.5194/egusphere-2024-3629, https://doi.org/10.5194/egusphere-2024-3629, 2024
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This study investigated aerosol-cloud interactions, focusing on organic nitrogen (ON) formation in the aqueous phase. Measurements were conducted in wintertime Italian Po Valley, using aerosol mass spectrometry. The fog was enriched in more hygroscopic inorganic compounds and ON, containing e.g. imidazoles. The formation of imidazole by aerosol-fog interactions could be confirmed for the first time in atmospheric observations. Findings highlight the role of fog in nitrogen aerosol formation.
Jie Zhang, Tianyu Zhu, Alexandra Catena, Yaowei Li, Margaret J. Schwab, Pengfei Liu, Akua Asa-Awuku, and James Schwab
Atmos. Chem. Phys., 24, 13445–13456, https://doi.org/10.5194/acp-24-13445-2024, https://doi.org/10.5194/acp-24-13445-2024, 2024
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This study shows the derived organic aerosol hygroscopicity under high-humidity conditions based on a simple optical scatter monitor system, including two nephelometric monitors (pDR-1500), when the aerosol chemical composition is already known.
Wei Yuan, Ru-Jin Huang, Chao Luo, Lu Yang, Wenjuan Cao, Jie Guo, and Huinan Yang
Atmos. Chem. Phys., 24, 13219–13230, https://doi.org/10.5194/acp-24-13219-2024, https://doi.org/10.5194/acp-24-13219-2024, 2024
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We characterized water-soluble oxidative potential (OP) levels in wintertime PM2.5 in the south and north of Beijing. Our results show that the volume-normalized dithiothreitol (DTTv) in the north was comparable to that in the south, while the mass-normalized dithiothreitol (DTTm) in the north was almost twice that in the south. Traffic-related emissions and biomass burning were the main sources of DTTv in the south, and traffic-related emissions contributed the most to DTTv in the north.
Mingfu Cai, Chenshuo Ye, Bin Yuan, Shan Huang, E Zheng, Suxia Yang, Zelong Wang, Yi Lin, Tiange Li, Weiwei Hu, Wei Chen, Qicong Song, Wei Li, Yuwen Peng, Baoling Liang, Qibin Sun, Jun Zhao, Duohong Chen, Jiaren Sun, Zhiyong Yang, and Min Shao
Atmos. Chem. Phys., 24, 13065–13079, https://doi.org/10.5194/acp-24-13065-2024, https://doi.org/10.5194/acp-24-13065-2024, 2024
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This study investigated the daytime secondary organic aerosol (SOA) formation in urban plumes. We observed a significant daytime SOA formation through gas–particle partitioning when the site was affected by urban plumes. A box model simulation indicated that urban pollutants (nitrogen oxide and volatile organic compounds) could enhance the oxidizing capacity, while the elevated volatile organic compounds were mainly responsible for promoting daytime SOA formation.
Qingxiao Meng, Yunjiang Zhang, Sheng Zhong, Jie Fang, Lili Tang, Yongcai Rao, Minfeng Zhou, Jian Qiu, Xiaofeng Xu, Jean-Eudes Petit, Olivier Favez, and Xinlei Ge
EGUsphere, https://doi.org/10.5194/egusphere-2024-2776, https://doi.org/10.5194/egusphere-2024-2776, 2024
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We developed a new method to reconstruct missing elemental carbon (EC) data in four Chinese cities from 2013 to 2023. Using machine learning, we accurately filled data gaps and introduced a new approach to analyze EC trends. Our findings reveal a significant decline in EC due to stricter pollution controls, though this slowed after 2020. This study provides a versatile framework for addressing data gaps and supports strategies to reduce urban air pollution and its climate impacts.
Yingjie Shen, Rudra P. Pokhrel, Amy P. Sullivan, Ezra J. T. Levin, Lauren A. Garofalo, Delphine K. Farmer, Wade Permar, Lu Hu, Darin W. Toohey, Teresa Campos, Emily V. Fischer, and Shane M. Murphy
Atmos. Chem. Phys., 24, 12881–12901, https://doi.org/10.5194/acp-24-12881-2024, https://doi.org/10.5194/acp-24-12881-2024, 2024
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The magnitude and evolution of brown carbon (BrC) absorption remain unclear, with uncertainty in climate models. Data from the WE-CAN airborne experiment show that model parameterizations overestimate the mass absorption cross section (MAC) of BrC. Observed decreases in BrC absorption with chemical markers are due to decreasing organic aerosol (OA) mass rather than a decreasing BrC MAC, which is currently implemented in models. Water-soluble BrC contributes 23 % of total absorption at 660 nm.
Qun He, Zhaowen Wang, Houfeng Liu, Pengju Xu, Rongbao Duan, Caihong Xu, Jianmin Chen, and Min Wei
Atmos. Chem. Phys., 24, 12775–12792, https://doi.org/10.5194/acp-24-12775-2024, https://doi.org/10.5194/acp-24-12775-2024, 2024
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Coastal environments provide an ideal setting for investigating the intermixing of terrestrial and marine aerosols. Terrestrial air mass constituted a larger number of microbes from anthropogenic and soil emissions, whereas saprophytic and gut microbes were predominant in marine samples. Mixed air masses indicated a fusion of marine and terrestrial aerosols, characterized by alterations in the ratio of pathogenic and saprophytic microbes when compared to either terrestrial or marine samples.
Rime El Asmar, Zongrun Li, David J. Tanner, Yongtao Hu, Susan O'Neill, L. Gregory Huey, M. Talat Odman, and Rodney J. Weber
Atmos. Chem. Phys., 24, 12749–12773, https://doi.org/10.5194/acp-24-12749-2024, https://doi.org/10.5194/acp-24-12749-2024, 2024
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Prescribed burning is an important method for managing ecosystems and preventing wildfires. However, smoke from prescribed fires can have a significant impact on air quality. Here, using a network of fixed sites and sampling throughout an extended prescribed burning period in 2 different years, we characterize emissions and evolutions of up to 8 h of PM2.5 mass, black carbon (BC), and brown carbon (BrC) in smoke from burning of forested lands in the southeastern USA.
Matthew Boyer, Diego Aliaga, Lauriane L. J. Quéléver, Silvia Bucci, Hélène Angot, Lubna Dada, Benjamin Heutte, Lisa Beck, Marina Duetsch, Andreas Stohl, Ivo Beck, Tiia Laurila, Nina Sarnela, Roseline C. Thakur, Branka Miljevic, Markku Kulmala, Tuukka Petäjä, Mikko Sipilä, Julia Schmale, and Tuija Jokinen
Atmos. Chem. Phys., 24, 12595–12621, https://doi.org/10.5194/acp-24-12595-2024, https://doi.org/10.5194/acp-24-12595-2024, 2024
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We analyze the seasonal cycle and sources of gases that are relevant for the formation of aerosol particles in the central Arctic. Since theses gases can form new particles, they can influence Arctic climate. We show that the sources of these gases are associated with changes in the Arctic environment during the year, especially with respect to sea ice. Therefore, the concentration of these gases will likely change in the future as the Arctic continues to warm.
Binyu Xiao, Fan Zhang, Zeyu Liu, Yan Zhang, Rui Li, Can Wu, Xinyi Wan, Yi Wang, Yubao Chen, Yong Han, Min Cui, Libo Zhang, Yingjun Chen, and Gehui Wang
EGUsphere, https://doi.org/10.5194/egusphere-2024-3433, https://doi.org/10.5194/egusphere-2024-3433, 2024
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Intermediate/semi-volatile organic compounds in both gas and particle phases from ship exhausts are enhanced due to the switch of fuels from low-sulfur to ultra-low-sulfur. The findings indicate that optimization is necessary for the forthcoming global implementation of an ultra-low-sulfur oil policy. Besides, we find that organic diagnostic markers of hopanes, in conjunction with the ratio of octadecanoic to tetradecanoic could be considered as potential tracers for HFO exhausts.
Mutian Ma, Laura-Hélèna Rivellini, Yichen Zong, Markus Kraft, Liya E. Yu, and Alex King Yin Lee
EGUsphere, https://doi.org/10.5194/egusphere-2024-3240, https://doi.org/10.5194/egusphere-2024-3240, 2024
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This work advances our understanding of emission and atmospheric evolution of black carbon (BC) particles in Singapore, a complex urban environment impacted by multiple local and regional combustion sources, based on the improved source apportionment analysis of real-time aerosol mass spectrometry measurement.
Hongyu Zhang, Shenbo Wang, Zhangsen Dong, Xiao Li, and Ruiqin Zhang
EGUsphere, https://doi.org/10.5194/egusphere-2024-2869, https://doi.org/10.5194/egusphere-2024-2869, 2024
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To address this, 12-year observational data in Zhengzhou were investigated and revealed that the resuspension of surrounding soil dust determined the rebound of crustal material concentrations after 2019, further elevating the particle pH. Therefore, the future ammonia reduction policies in North China may not lead to a rapid increase in particle acidity buffering by the crustal materials, but it is necessary to consider synergistic control with dust sources.
Haley M. Royer, Michael T. Sheridan, Hope E. Elliott, Nurun Nahar Lata, Zezhen Cheng, Swarup China, Zihua Zhu, Andrew P. Ault, and Cassandra J. Gaston
EGUsphere, https://doi.org/10.5194/egusphere-2024-3288, https://doi.org/10.5194/egusphere-2024-3288, 2024
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Saharan dust transported across the Atlantic to the Caribbean, South America, and North America is hypothesized to undergo chemical processing by inorganic and organic acids that enhances cloud droplet formation, nutrient availability, and reflectivity of. In this study, chemical analysis performed on African dust deposited over Barbados shows that acid tracers are found mostly on sea salt and smoke particles, rather than dust, indicating that dust particles undergo minimal chemical processing.
Imad El Haddad, Danielle Vienneau, Kaspar R. Daellenbach, Robin Modini, Jay G. Slowik, Abhishek Upadhyay, Petros N. Vasilakos, David Bell, Kees de Hoogh, and Andre S. H. Prevot
Atmos. Chem. Phys., 24, 11981–12011, https://doi.org/10.5194/acp-24-11981-2024, https://doi.org/10.5194/acp-24-11981-2024, 2024
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This opinion paper explores how advances in aerosol science inform our understanding of the health impacts of outdoor particulate pollution. We advocate for a shift in the way we target PM pollution, focusing on the most harmful anthropogenic emissions. We highlight key observations, modelling developments, and emission measurements needed to achieve this shift.
Yu Huang, Xingru Li, Dan Dan Huang, Ruoyuan Lei, Binhuang Zhou, Yunjiang Zhang, and Xinlei Ge
EGUsphere, https://doi.org/10.5194/egusphere-2024-2757, https://doi.org/10.5194/egusphere-2024-2757, 2024
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This work performed a comprehensive investigation on the chemical and optical properties of the brown carbon in PM2.5 samples collected in Nanjing, China. In particular, we used the machine learning approach to identify a list of key BrC species, which can be a good reference for future studies. Our findings extend the understanding on BrC properties and are valuable to the assessment of its impact on air quality and radiative forcing.
Pramod Kumar, Khushboo Sharma, Ankita Malu, Rajeev Rajak, Aparna Gupta, Bidyutjyoti Baruah, Shailesh Yadav, Thupstan Angchuk, Jayant Sharma, Rakesh Kumar Ranjan, Anil Kumar Misra, and Nishchal Wanjari
Atmos. Chem. Phys., 24, 11585–11601, https://doi.org/10.5194/acp-24-11585-2024, https://doi.org/10.5194/acp-24-11585-2024, 2024
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This work monitors and assesses air pollution, especially black and brown carbon, its controlling factor, and its effect on the environment of Sikkim Himalayan region. The huge urban sprawl in recent decades has led to regional human-induced air pollution in the region. Black carbon was highest in April 2021 and March 2022, exceeding the WHO limit. The monsoon season causes huge rainfall over the region, which reduces the pollutants by scavenging (rainout and washout).
Maria P. Velásquez-García, K. Santiago Hernández, James A. Vergara-Correa, Richard J. Pope, Miriam Gómez-Marín, and Angela M. Rendón
Atmos. Chem. Phys., 24, 11497–11520, https://doi.org/10.5194/acp-24-11497-2024, https://doi.org/10.5194/acp-24-11497-2024, 2024
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In the Aburrá Valley, northern South America, local emissions determine air quality conditions. However, we found that external sources, such as regional fires, Saharan dust, and volcanic emissions, increase particulate concentrations and worsen chemical composition by introducing elements like heavy metals. Dry winds and source variability contribute to seasonal influences on these events. This study assesses the air quality risks posed by such events, which can affect broad regions worldwide.
Meng Wang, Qiyuan Wang, Steven Sai Hang Ho, Jie Tian, Yong Zhang, Shun-cheng Lee, and Junji Cao
Atmos. Chem. Phys., 24, 11175–11189, https://doi.org/10.5194/acp-24-11175-2024, https://doi.org/10.5194/acp-24-11175-2024, 2024
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We studied nitrogen-containing organic compounds (NOCs) in particulate matter <2.5 µm particles on the southeastern Tibetan Plateau. We found that biomass burning and transboundary transport are the main sources of NOCs in the high-altitude area. Understanding these aerosol sources informs how they add to regional and potentially global climate changes. Our findings could help shape effective environmental policies to enhance air quality and address climate impacts in this sensitive region.
Jinbo Wang, Jiaping Wang, Yuxuan Zhang, Tengyu Liu, Xuguang Chi, Xin Huang, Dafeng Ge, Shiyi Lai, Caijun Zhu, Lei Wang, Qiaozhi Zha, Ximeng Qi, Wei Nie, Congbin Fu, and Aijun Ding
Atmos. Chem. Phys., 24, 11063–11080, https://doi.org/10.5194/acp-24-11063-2024, https://doi.org/10.5194/acp-24-11063-2024, 2024
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In this study, we found large spatial discrepancies in the physical and chemical properties of black carbon over the Tibetan Plateau (TP). Elevated anthropogenic emissions from low-altitude regions can significantly change the mass concentration, mixing state and chemical composition of black-carbon-containing aerosol in the TP region, further altering its light absorption ability. Our study emphasizes the vulnerability of remote plateau regions to intense anthropogenic influences.
Liyuan Zhou, Qianyun Liu, Christian M. Salvador, Michael Le Breton, Mattias Hallquist, Jian Zhen Yu, Chak K. Chan, and Åsa M. Hallquist
Atmos. Chem. Phys., 24, 11045–11061, https://doi.org/10.5194/acp-24-11045-2024, https://doi.org/10.5194/acp-24-11045-2024, 2024
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Our research on city bus emissions reveals that alternative fuels (compressed natural gas and biofuels) reduce fresh particle emissions compared to diesel. However, all fuels lead to secondary air pollution. Aiming at guiding better environmental policies, we studied 76 buses using advanced emission measurement techniques. This work sheds light on the complex effects of bus fuels on urban air quality, emphasizing the need for comprehensive evaluations of future transportation technologies.
Xu Yang, Fobang Liu, Shuqi Yang, Yuling Yang, Yanan Wang, Jingjing Li, Mingyu Zhao, Zhao Wang, Kai Wang, Chi He, and Haijie Tong
Atmos. Chem. Phys., 24, 11029–11043, https://doi.org/10.5194/acp-24-11029-2024, https://doi.org/10.5194/acp-24-11029-2024, 2024
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A study in the rural North China Plain showed environmentally persistent free radicals (EPFRs) in atmospheric particulate matter (PM), with a notable water-soluble fraction likely from atmospheric oxidation during transport. Significant positive correlations between EPFRs and the water-soluble oxidative potential of PM2.5 were found, primarily attributable to the water-soluble fractions of EPFRs. These findings emphasize understanding EPFRs' atmospheric evolution for climate and health impacts.
Genevieve Rose Lorenzo, Luke D. Ziemba, Avelino F. Arellano, Mary C. Barth, Ewan C. Crosbie, Joshua P. DiGangi, Glenn S. Diskin, Richard Ferrare, Miguel Ricardo A. Hilario, Michael A. Shook, Simone Tilmes, Jian Wang, Qian Xiao, Jun Zhang, and Armin Sorooshian
EGUsphere, https://doi.org/10.5194/egusphere-2024-2604, https://doi.org/10.5194/egusphere-2024-2604, 2024
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Novel aerosol hygroscopicity analysis of CAMP2Ex field campaign data show low aerosol hygroscopicity values in Southeast Asia. Organic carbon from smoke decreases hygroscopicity to levels more like those in continental than in polluted marine regions. Hygroscopicity changes at cloud level demonstrate how surface particles impact clouds in the region affecting model representation of aerosol and cloud interactions in similar polluted marine regions with high organic carbon emissions.
Cited articles
Alfarra, M. R., Paulsen, D., Gysel, M., Garforth, A. A., Dommen, J.,
Prévôt, A. S. H., Worsnop, D. R., Baltensperger, U., and Coe, H.: A
mass spectrometric study of secondary organic aerosols formed from the
photooxidation of anthropogenic and biogenic precursors in a reaction
chamber, Atmos. Chem. Phys., 6, 5279–5293,
https://doi.org/10.5194/acp-6-5279-2006, 2006.
Alvarez-Aviles, L., Simpson, W. R., Douglas, T. A., Sturm, M., Perovich, D.,
and Domine, F.: Frost flower chemical composition during growth and its
implications for aerosol production and bromine activation, J. Geophys.
Res.-Atmos., 113, D21304, https://doi.org/10.1029/2008jd010277, 2008.
Alves, C. A. and Pio, C. A.: Secondary organic compounds in atmospheric
aerosols: Speciation and formation mechanisms, J. Brazil. Chem. Soc., 16,
1017–1029, https://doi.org/10.1590/s0103-50532005000600020, 2005.
Arrigo, K. R., van Dijken, G. L., and Bushinsky, S.: Primary production in
the Southern Ocean, 1997–2006, J. Geophys. Res.-Oceans, 113, C08004,
https://doi.org/10.1029/2007jc004551, 2008.
Asmi, E., Frey, A., Virkkula, A., Ehn, M., Manninen, H. E., Timonen, H.,
Tolonen-Kivimäki, O., Aurela, M., Hillamo, R., and Kulmala, M.:
Hygroscopicity and chemical composition of Antarctic sub-micrometre aerosol
particles and observations of new particle formation, Atmos. Chem. Phys., 10,
4253–4271, https://doi.org/10.5194/acp-10-4253-2010, 2010.
Asmi, E., Neitola, K., Teinila, K., Rodriguez, E., Virkkula, A., Backman, J.,
Bloss, M., Jokela, J., Lihavainen, H., De Leeuw, G., Paatero, J., Aaltonen,
V., Mei, M., Gambarte, G., Copes, G., Albertini, M., Fogwill, G. P., Ferrara,
J., Barlasina, M. E., and Sanchez, R.: Primary sources control the
variability of aerosol optical properties in the Antarctic Peninsula, Tellus
B, 70, 1, https://doi.org/10.1080/16000889.2017.1414571, 2018.
Attwood, A. R., Washenfelder, R. A., Brock, C. A., Hu, W., Baumann, K.,
Campuzano-Jost, P., Day, D. A., Edgerton, E. S., Murphy, D. M., Palm, B. B.,
McComiskey, A., Wagner, N. L., de Sa, S. S., Ortega, A., Martin, S. T.,
Jimenez, J. L., and Brown, S. S.: Trends in sulfate and organic aerosol mass
in the Southeast U.S.: Impact on aerosol optical depth and radiative forcing,
Geophys. Res. Lett., 41, 7701–7709, 10.1002/2014gl061669, 2014.
Barbaro, E., Kirchgeorg, T., Zangrando, R., Vecchiato, M., Piazza, R.,
Barbante, C., and Garnbaro, A.: Sugars in Antarctic aerosol, Atmos. Environ.,
118, 135–144, https://doi.org/10.1016/j.atmosenv.2015.07.047, 2015a.
Barbaro, E., Zangrando, R., Vecchiato, M., Piazza, R., Cairns, W. R. L.,
Capodaglio, G., Barbante, C., and Gambaro, A.: Free amino acids in Antarctic
aerosol: potential markers for the evolution and fate of marine aerosol,
Atmos. Chem. Phys., 15, 5457–5469, https://doi.org/10.5194/acp-15-5457-2015,
2015b.
Barbaro, E., Zangrando, R., Kirchgeorg, T., Bazzano, A., Illuminati, S.,
Annibaldi, A., Rella, S., Truzzi, C., Grotti, M., Ceccarini, A., Malitesta,
C., Scarponi, G., and Gambaro, A.: An integrated study of the chemical
composition of Antarctic aerosol to investigate natural and anthropogenic
sources, Environ. Chem., 13, 867–876, 10.1071/en16056, 2016.
Barbaro, E., Padoan, S., Kirchgeorg, T., Zangrando, R., Toscano, G.,
Barbante, C., and Gambaro, A.: Particle size distribution of inorganic and
organic ions in coastal and inland Antarctic aerosol, Environ. Sci. Pollut.
R., 24, 2724–2733, https://doi.org/10.1007/s11356-016-8042-x, 2017.
Beaton, A. E. and Tukey, J. W.: The Fitting of Power Series, Meaning
Polynomials, Illustrated on Band-Spectroscopic Data, Technometrics, 16,
147–185, https://doi.org/10.2307/1267936, 1974.
Bintanja, R., Severijns, C., Haarsma, R., and Hazeleger, W.: The future of
Antarctica's surface winds simulated by a high-resolution global climate
model: 1. Model description and validation, J. Geophys. Res.-Atmos., 119,
7136–7159, https://doi.org/10.1002/2013jd020847, 2014.
Bodhaine, B. A.: Aerosol measurements at four background sites, J. Geophys.
Res.-Oceans, 88, 10753–10768, 1983.
Bodhaine, B. A., Deluisi, J. J., Harris, J. M., Houmere, P., and Bauman, S.:
Aerosol measurements at the South Pole, Tellus B, 38, 223–235, 1986.
Bromwich, D. H., Nicolas, J. P., Monaghan, A. J., Lazzara, M. A., Keller, L.
M., Weidner, G. A., and Wilson, A. B.: Central West Antarctica among the most
rapidly warming regions on Earth, Nat. Geosci., 6, 139–145,
https://doi.org/10.1038/ngeo1671, 2013.
Cadle, R. D., Fischer, W. H., Frank, E. R., and Lodge, J. P.: Particles in
Antarctic Atmosphere, J. Atmos. Sci., 25, 100–103,
https://doi.org/10.1175/1520-0469(1968)025<0100:pitaa>2.0.co;2, 1968.
Charbouillot, T., Gorini, S., Voyard, G., Parazols, M., Brigante, M.,
Deguillaume, L., Delort, A. M., and Mailhot, G.: Mechanism of carboxylic acid
photooxidation in atmospheric aqueous phase: Formation, fate and reactivity,
Atmos. Environ., 56, 1–8, https://doi.org/10.1016/j.atmosenv.2012.03.079, 2012.
Cheung, K. L., Ntziachristos, L., Tzamkiozis, T., Schauer, J. J., Samaras,
Z., Moore, K. F., and Sioutas, C.: Emissions of Particulate Trace Elements,
Metals and Organic Species from Gasoline, Diesel, and Biodiesel Passenger
Vehicles and Their Relation to Oxidative Potential, Aerosol Sci. Tech., 44,
500–513, https://doi.org/10.1080/02786821003758294, 2010.
Claeys, M., Szmigielski, R., Kourtchev, I., Van der Veken, P., Vermeylen, R.,
Maenhaut, W., Jaoui, M., Kleindienst, T. E., Lewandowski, M., and Offenberg,
J. H.: Hydroxydicarboxylic acids: markers for secondary organic aerosol from
the photooxidation of α-pinene, Environ. Sci. Technol., 41,
1628–1634, 2007.
Cowie, G. L. and Hedges, J. I.: Sources and reactivities of amino acids in a
coastal marine environment, Limnol. Oceanogr., 37, 703–724,
https://doi.org/10.4319/lo.1992.37.4.0703, 1992.
Croft, B., Martin, R. V., Leaitch, W. R., Tunved, P., Breider, T. J.,
D'Andrea, S. D., and Pierce, J. R.: Processes controlling the annual cycle of
Arctic aerosol number and size distributions, Atmos. Chem. Phys., 16,
3665–3682, https://doi.org/10.5194/acp-16-3665-2016, 2016a.
Croft, B., Wentworth, G. R., Martin, R. V., Leaitch, W. R., Murphy, J. G.,
Murphy, B. N., Kodros, J. K., Abbatt, J. P. D., and Pierce, J. R.:
Contribution of Arctic seabird-colony ammonia to atmospheric particles and
cloud-albedo radiative effect, Nat. Commun., 7, 13444,
https://doi.org/10.1038/ncomms13444, 2016b.
Dall'Osto, M., Ceburnis, D., Monahan, C., Worsnop, D. R., Bialek, J.,
Kulmala, M., Kurten, T., Ehn, M., Wenger, J., Sodeau, J., Healy, R., and
O'Dowd, C.: Nitrogenated and aliphatic organic vapors as possible drivers for
marine secondary organic aerosol growth, J. Geophys. Res.-Atmos., 117,
D12311, https://doi.org/10.1029/2012jd017522, 2012.
Dall'Osto, M., Ovadnevaite, J., Paglione, M., Beddows, D. C. S., Ceburnis,
D., Cree, C., Cortes, P., Zamanillo, M., Nunes, S. O., Perez, G. L.,
Ortega-Retuerta, E., Emelianov, M., Vaque, D., Marrase, C., Estrada, M.,
Sala, M. M., Vidal, M., Fitzsimons, M. F., Beale, R., Airs, R., Rinaldi, M.,
Decesari, S., Facchini, M. C., Harrison, R. M., O'Dowd, C., and Simo, R.:
Antarctic sea ice region as a source of biogenic organic nitrogen in
aerosols, Scientific Reports, 7, 6047, https://doi.org/10.1038/s41598-017-06188-x, 2017.
Davis, L. S., Harcourt, R. G., and Bradshaw, C. J. A.: The winter migration
of Adelie penguins breeding in the Ross Sea sector of Antarctica, Polar
Biol., 24, 593–597, https://doi.org/10.1007/s003000100256, 2001.
Defelice, T. P., Saxena, V. K., and Yu, S. C.: On the measurements of cloud
condensation nuclei at Palmer Station, Antarctica, Atmos. Environ., 31,
4039–4044, https://doi.org/10.1016/s1352-2310(97)00250-1, 1997.
Domine, F., Sparapani, R., Ianniello, A., and Beine, H. J.: The origin of sea
salt in snow on Arctic sea ice and in coastal regions, Atmos. Chem. Phys., 4,
2259–2271, https://doi.org/10.5194/acp-4-2259-2004, 2004.
Draxier, R. R. and Hess, G. D.: An overview of the HYSPLIT_4 modelling
system for trajectories, dispersion and deposition, Aust. Meteorol. Mag., 47,
295–308, 1998.
Frossard, A. A., Shaw, P. M., Russell, L. M., Kroll, J. H., Canagaratna, M.
R., Worsnop, D. R., Quinn, P. K., and Bates, T. S.: Springtime Arctic haze
contributions of submicron organic particles from European and Asian
combustion sources, J. Geophys. Res.-Atmos., 116, D05205,
https://doi.org/10.1029/2010jd015178, 2011.
Frossard, A. A., Russell, L. M., Keene, W. C., Kieber, D. J., Quinn, P. K.,
and Bates, T. S.: Regional Signatures in the Organic Composition of Marine
Aerosol Particles, in: AIP Conference Proceedings, 19th International
Conference on Nucleation and Atmospheric Aerosols (ICNAA), Colorado State
Univ, Ctr Arts, Fort Collins, CO, 2013, 543–546, 2013.
Frossard, A. A., Russell, L. M., Burrows, S. M., Elliott, S. M., Bates, T.
S., and Quinn, P. K.: Sources and composition of submicron organic mass in
marine aerosol particles, J. Geophys. Res.-Atmos., 119, 12977–13003,
https://doi.org/10.1002/2014jd021913, 2014a.
Frossard, A. A., Russell, L. M., Massoli, P., Bates, T. S., and Quinn, P. K.:
Side-by-Side Comparison of Four Techniques Explains the Apparent Differences
in the Organic Composition of Generated and Ambient Marine Aerosol Particles,
Aerosol Sci. Tech., 48, V–X, https://doi.org/10.1080/02786826.2013.879979, 2014b.
Gagosian, R. B. and Stuermer, D. H.: The cycling of biogenic compounds and
their diagenetically transformed products in seawater, Mar. Chem., 5,
605–632, 1977.
Giordano, M. R., Kalnajs, L. E., Avery, A., Goetz, J. D., Davis, S. M., and
DeCarlo, P. F.: A missing source of aerosols in Antarctica – beyond
long-range transport, phytoplankton, and photochemistry, Atmos. Chem. Phys.,
17, 1–20, https://doi.org/10.5194/acp-17-1-2017, 2017.
Gordon, M. and Taylor, P. A.: Measurements of blowing snow, Part I: Particle
shape, size distribution, velocity, and number flux at Churchill, Manitoba,
Canada, Cold Reg. Sci. Technol., 55, 63–74,
https://doi.org/10.1016/j.coldregions.2008.05.001, 2009.
Goring, D. G. and Nikora, V. I.: Despiking acoustic Doppler velocimeter data,
J. Hydraul. Eng.-ASCE, 128, 117–126,
https://doi.org/10.1061/(asce)0733-9429(2002)128:1(117), 2002.
Gras, J. L.: Condensation nucleus size distribution at Mawson, Antarctica –
microphysics and chemistry, Atmos. Environ. A-Gen., 27, 1427–1434,
https://doi.org/10.1016/0960-1686(93)90128-l, 1993.
Guzman-Morales, J., Frossard, A. A., Corrigan, A. L., Russell, L. M., Liu,
S., Takahama, S., Taylor, J. W., Allan, J., Coe, H., Zhao, Y., and Goldstein,
A. H.: Estimated contributions of primary and secondary organic aerosol from
fossil fuel combustion during the CalNex and Cal-Mex campaigns, Atmos.
Environ., 88, 330–340, 10.1016/j.atmosenv.2013.08.047, 2014.
Hansen, A. D. A., Bodhaine, B. A., Dutton, E. G., and Schnell, R. C.: Aerosol
Black Carbon Measurements at the South-Pole – Initial Results, 1986–1987,
Geophys. Res. Lett., 15, 1193–1196, https://doi.org/10.1029/GL015i011p01193, 1988.
Hansen, A. D. A., Lowenthal, D. H., Chow, J. C., and Watson, J. G.: Black
carbon aerosol at McMurdo station, Antarctica, J. Air Waste Manage., 51,
593–600, 2001.
Hara, K., Osada, K., Kido, M., Hayashi, M., Matsunaga, K., Iwasaka, Y.,
Yamanouchi, T., Hashida, G., and Fukatsu, T.: Chemistry of sea-salt particles
and inorganic halogen species in Antarctic regions: Compositional differences
between coastal and inland stations, J. Geophys. Res.-Atmos., 109, D20208,
https://doi.org/10.1029/2004JD004713, 2004.
Hara, K., Osada, K., Kido, M., Matsunaga, K., Iwasaka, Y., Hashida, G., and
Yamanouchi, T.: Variations of constituents of individual sea-salt particles
at Syowa station, Antarctica, Tellus B, 57, 230–246,
https://doi.org/10.1111/j.1600-0889.2005.00142.x, 2005.
Hara, K., Osada, K., Yabuki, M., Hashida, G., Yamanouchi, T., Hayashi, M.,
Shiobara, M., Nishita, C., and Wada, M.: Haze episodes at Syowa Station,
coastal Antarctica: Where did they come from?, J. Geophys. Res.-Atmos., 115,
D14205, https://doi.org/10.1029/2009JD012582, 2010.
Harder, S., Warren, S. G., and Charlson, R. J.: Sulfate in air and snow at
the South Pole: Implications for transport and deposition at sites with low
snow accumulation, J. Geophys. Res.-Atmos., 105, 22825–22832, 2000.
Hartigan, J. A. and Wong, M. A.: Algorithm AS 136: A k-means clustering
algorithm, J. Roy. Stat. Soc. C-App., 28, 100–108, 1979.
Hawkins, L. N. and Russell, L.: Polysaccharides, Proteins, and Phytoplankton
Fragments: Four Chemically Distinct Types of Marine Primary Organic Aerosol
Classified by Single Particle Spectromicroscopy, Adv. Meteorol., 14, 612132,
https://doi.org/10.1155/2010/612132, 2010.
Hofmann, D.: Balloon-borne measurements of middle atmosphere aerosols and
trace gases in Antarctica, Rev. Geophy., 26, 113–130, 1988.
Hofmann, D. J., Rosen, J. M., Harder, J. A., and Rolf, S. R.: Ozone and
aerosol measurements in the springtime Antarctic Stratosphere in 1985,
Geophys. Res. Lett., 13, 1252–1255, https://doi.org/10.1029/GL013i012p01252, 1986.
Hogan, A. W.: Antarctic aerosols, J. Appl. Meteorol., 14, 550–559,
https://doi.org/10.1175/1520-0450(1975)014<0550:aa>2.0.co;2, 1975.
Hogan, A. W. and Barnard, S.: Seasonal and frontal variation in Antarctic
aerosol concentrations, J. Appl. Meteorol., 17, 1458–1465,
https://doi.org/10.1175/1520-0450(1978)017<1458:safvia>2.0.co;2, 1978.
Holland, P. R.: The seasonality of Antarctic sea ice trends, Geophys. Res.
Lett., 41, 4230–4237, https://doi.org/10.1002/2014gl060172, 2014.
Huang, J. and Jaeglé, L.: Wintertime enhancements of sea salt aerosol in
polar regions consistent with a sea ice source from blowing snow, Atmos.
Chem. Phys., 17, 3699–3712, https://doi.org/10.5194/acp-17-3699-2017, 2017.
IPCC: Summary for policymakers in climate change 2013: the physical science
basis, contribution of working group I to the fifth assessment report of the
intergovernmental panel on climate change, edited by: Stocker, T. F., Qin,
D., Plattner, G. K., Tignor, M., Allen, S. K., Boschung, J., Nauels, A., Xia,
Y., Bex, V., and Midgley, P. M., Cambridge Univ Press, Cambridge, UK and New
York, 2013.
Jourdain, B. and Legrand, M.: Year-round records of bulk and size-segregated
aerosol composition and HCl and HNO3 levels in the Dumont d'Urville
(coastal Antarctica) atmosphere: Implications for sea-salt aerosol
fractionation in the winter and summer, J. Geophys. Res.-Atmos., 107, 4645,
https://doi.org/10.1029/2002jd002471, 2002.
Jourdain, B., Preunkert, S., Cerri, O., Castebrunet, H., Udisti, R., and
Legrand, M.: Year-round record of size-segregated aerosol composition in
central Antarctica (Concordia station): Implications for the degree of
fractionation of sea-salt particles, J. Geophys. Res.-Atmos., 113, D14308,
https://doi.org/10.1029/2007jd009584, 2008.
Kalnajs, L. E., Avallone, L. M., and Toohey, D. W.: Correlated measurements
of ozone and particulates in the Ross Island region, Antarctica, Geophys.
Res. Lett., 40, 6319–6323, 10.1002/2013gl058422, 2013.
Kawamura, K. and Gagosian, R. B.: Implications of omega-oxocarboxylic acids
in the remote marine atmosphere for photooxidation of unsaturated fatty
acids, Nature, 325, 330–332, https://doi.org/10.1038/325330a0, 1987.
Khan, A. L., McMeeking, G. R., Schwarz, J. P., Xian, P., Welch, K. A., Berry
Lyons, W., and McKnight, D. M.: Near-Surface Refractory Black Carbon
Observations in the Atmosphere and Snow in the McMurdo Dry Valleys,
Antarctica, and Potential Impacts of Foehn Winds, J. Geophys. Res.-Atmos.,
123, 2877–2887, 2018.
Kim, J., Yoon, Y. J., Gim, Y., Kang, H. J., Choi, J. H., Park, K.-T., and
Lee, B. Y.: Seasonal variations in physical characteristics of aerosol
particles at the King Sejong Station, Antarctic Peninsula, Atmos. Chem.
Phys., 17, 12985–12999, https://doi.org/10.5194/acp-17-12985-2017, 2017.
Korhonen, H., Carslaw, K. S., Spracklen, D. V., Mann, G. W., and Woodhouse,
M. T.: Influence of oceanic dimethyl sulfide emissions on cloud condensation
nuclei concentrations and seasonality over the remote Southern Hemisphere
oceans: A global model study, J. Geophys. Res.-Atmos., 113, D15204,
https://doi.org/10.1029/2007jd009718, 2008.
Kuznetsova, M., Lee, C., and Aller, J.: Characterization of the proteinaceous
matter in marine aerosols, Mar. Chem., 96, 359–377,
https://doi.org/10.1016/j.marchem.2005.03.007, 2005.
Kyrö, E.-M., Kerminen, V.-M., Virkkula, A., Dal Maso, M., Parshintsev,
J., Ruíz-Jimenez, J., Forsström, L., Manninen, H. E., Riekkola,
M.-L., Heinonen, P., and Kulmala, M.: Antarctic new particle formation from
continental biogenic precursors, Atmos. Chem. Phys., 13, 3527–3546,
https://doi.org/10.5194/acp-13-3527-2013, 2013.
Lambeck, K., Esat, T. M., and Potter, E. K.: Links between climate and sea
levels for the past three million years, Nature, 419, 199–206,
https://doi.org/10.1038/nature01089, 2002.
Leaitch, W. R., Russell, L. M., Liu, J., Kolonjari, F., Toom, D., Huang, L.,
Sharma, S., Chivulescu, A., Veber, D., and Zhang, W.: Organic functional
groups in the submicron aerosol at 82.5∘ N, 62.5∘ W from
2012 to 2014, Atmos. Chem. Phys., 18, 3269–3287,
https://doi.org/10.5194/acp-18-3269-2018, 2018.
Legrand, M., Ducroz, F., Wagenbach, D., Mulvaney, R., and Hall, J.: Ammonium
in coastal Antarctic aerosol and snow: Role of polar ocean and penguin
emissions, J. Geophys. Res.-Atmos., 103, 11043–11056, https://doi.org/10.1029/97jd01976,
1998.
Legrand, M., Gros, V., Preunkert, S., Sarda-Esteve, R., Thierry, A. M., Pepy,
G., and Jourdain, B.: A reassessment of the budget of formic and acetic acids
in the boundary layer at Dumont d'Urville (coastal Antarctica): The role of
penguin emissions on the budget of several oxygenated volatile organic
compounds, J. Geophys. Res.-Atmos., 117, D06308, https://doi.org/10.1029/2011jd017102,
2012.
Legrand, M., Preunkert, S., Weller, R., Zipf, L., Elsässer, C., Merchel,
S., Rugel, G., and Wagenbach, D.: Year-round record of bulk and
size-segregated aerosol composition in central Antarctica (Concordia site) –
Part 2: Biogenic sulfur (sulfate and methanesulfonate) aerosol, Atmos. Chem.
Phys., 17, 14055–14073, https://doi.org/10.5194/acp-17-14055-2017, 2017a.
Legrand, M., Preunkert, S., Wolff, E., Weller, R., Jourdain, B., and
Wagenbach, D.: Year-round records of bulk and size-segregated aerosol
composition in central Antarctica (Concordia site) – Part 1: Fractionation
of sea-salt particles, Atmos. Chem. Phys., 17, 14039–14054,
https://doi.org/10.5194/acp-17-14039-2017, 2017b.
Lin, Y.-C., Tsai, C.-J., Wu, Y.-C., Zhang, R., Chi, K.-H., Huang, Y.-T., Lin,
S.-H., and Hsu, S.-C.: Characteristics of trace metals in traffic-derived
particles in Hsuehshan Tunnel, Taiwan: size distribution, potential source,
and fingerprinting metal ratio, Atmos. Chem. Phys., 15, 4117–4130,
https://doi.org/10.5194/acp-15-4117-2015, 2015.
Liu, J., Lewis, S., and Russell, L. M.: Organic and Elemental Composition of
Submicron Aerosol Particles during AWARE at McMurdo Station, Antarctica,
https://doi.org/10.6075/J0WM1BKV, 2018.
Loureiro, A., Vasconcellos, M., and Pereira, E.: Trace element determination
in aerosols from the Antarctic Peninsula by neutron activation analysis, J.
Radioanal. Nucl. Ch., 159, 21–28, 1992.
Lyver, P. O., Barron, M., Barton, K. J., Ainley, D. G., Pollard, A., Gordon,
S., McNeill, S., Ballard, G., and Wilson, P. R.: Trends in the Breeding
Population of Adelie Penguins in the Ross Sea, 1981–2012: A Coincidence of
Climate and Resource Extraction Effects, Plos One, 9,
https://doi.org/10.1371/journal.pone.0091188, 2014.
Mace, K. A., Duce, R. A., and Tindale, N. W.: Organic nitrogen in rain and
aerosol at Cape Grim, Tasmania, Australia, J. Geophys. Res.-Atmos., 108,
4338, https://doi.org/10.1029/2002jd003051, 2003a.
Mace, K. A., Kubilay, N., and Duce, R. A.: Organic nitrogen in rain and
aerosol in the eastern Mediterranean atmosphere: An association with
atmospheric dust, J. Geophys. Res.-Atmos., 108, 4320,
https://doi.org/10.1029/2002jd002997, 2003b.
Mandalakis, M., Apostolaki, M., Tziaras, T., Polymenakou, P., and Stephanou,
E. G.: Free and combined amino acids in marine background atmospheric
aerosols over the Eastern Mediterranean, Atmos. Environ., 45, 1003–1009,
https://doi.org/10.1016/j.atmosenv.2010.10.046, 2011.
Maria, S. F., Russell, L. M., Turpin, B. J., and Porcja, R. J.: FTIR
measurements of functional groups and organic mass in aerosol samples over
the Caribbean, Atmos. Environ., 36, 5185–5196,
https://doi.org/10.1016/s1352-2310(02)00654-4, 2002.
Matsumoto, K. and Uematsu, M.: Free amino acids in marine aerosols over the
western North Pacific Ocean, Atmos. Environ., 39, 2163–2170,
https://doi.org/10.1016/j.atmosenv.2004.12.022, 2005.
Mazzera, D. M., Lowenthal, D. H., Chow, J. C., and Watson, J. G.: Sources of
PM10 and sulfate aerosol at McMurdo station, Antarctica, Chemosphere,
45, 347–356, https://doi.org/10.1016/s0045-6535(00)00591-9, 2001a.
Mazzera, D. M., Lowenthal, D. H., Chow, J. C., Watson, J. G., and Grubisic,
V.: PM10 measurements at McMurdo Station, Antarctica, Atmos. Environ.,
35, 1891–1902, https://doi.org/10.1016/s1352-2310(00)00409-x, 2001b.
McCoy, D. T., Burrows, S. M., Wood, R., Grosvenor, D. P., Elliott, S. M., Ma,
P.-L., Rasch, P. J., and Hartmann, D. L.: Natural aerosols explain seasonal
and spatial patterns of Southern Ocean cloud albedo, Sci. Adv., 1, e1500157,
https://doi.org/10.1126/sciadv.1500157, 2015.
McNeill, V. F.: Aqueous Organic Chemistry in the Atmosphere: Sources and
Chemical Processing of Organic Aerosols, Environ. Sci. Technol., 49,
1237–1244, https://doi.org/10.1021/es5043707, 2015.
Milne, P. J. and Zika, R. G.: Amino-acid nitrogen in atmospheric aerosols –
occurrence, sources and photochemical modification, J. Atmos. Chem., 16,
361–398, https://doi.org/10.1007/bf01032631, 1993.
Minikin, A., Legrand, M., Hall, J., Wagenbach, D., Kleefeld, C., Wolff, E.,
Pasteur, E. C., and Ducroz, F.: Sulfur-containing species (sulfate and
methanesulfonate) in coastal Antarctic aerosol and precipitation, J. Geophys.
Res.-Atmos. 103, 10975–10990, 1998.
Mishra, V. K., Kim, K.-H., Hong, S., and Lee, K.: Aerosol composition and its
sources at the King Sejong Station, Antarctic peninsula, Atmos. Environ., 38,
4069–4084, 2004.
Modini, R. L., Frossard, A. A., Ahlm, L., Russell, L. M., Corrigan, C. E.,
Roberts, G. C., Hawkins, L. N., Schroder, J. C., Bertram, A. K., Zhao, R.,
Lee, A. K. Y., Abbatt, J. P. D., Lin, J., Nenes, A., Wang, Z., Wonaschutz,
A., Sorooshian, A., Noone, K. J., Jonsson, H., Seinfeld, J. H., Toom-Sauntry,
D., Macdonald, A. M., and Leaitch, W. R.: Primary marine aerosol-cloud
interactions off the coast of California, J. Geophys. Res.-Atmos., 120,
4282–4303, https://doi.org/10.1002/2014jd022963, 2015.
Olson, M. R., Garcia, M. V., Robinson, M. A., Van Rooy, P., Dietenberger, M.
A., Bergin, M., and Schauer, J. J.: Investigation of black and brown carbon
multiple-wavelength-dependent light absorption from biomass and fossil fuel
combustion source emissions, J. Geophys. Res.-Atmos., 120, 6682–6697,
https://doi.org/10.1002/2014jd022970, 2015.
Ondov, J. M., Gladney, E. S., Zoller, W. H., Duce, R. A., and Jones, A. G.:
Atmospheric particulates at South-Pole station, Antarct. J. US, 8, 182–183,
1973a.
Ondov, J. M., Gladney, E. S., Zoller, W. H., Duce, R. A., and Jones, A. G.:
Atmospheric particulates at South-Pole station, Antarct. J. US, 8, 182–183,
1973b.
Paatero, P.: Least squares formulation of robust non-negative factor
analysis, Chemometr. Intell. Lab., 37, 23–35,
https://doi.org/10.1016/s0169-7439(96)00044-5, 1997.
Paatero, P. and Tapper, U.: Positive Matrix Factorization: A Non-Negative
Factor Model with Optimal Utilization of Error Estimates of Data Values,
Environmetrics, 5, 111–126, https://doi.org/10.1002/env.3170050203, 1994.
Parungo, F., Bodhaine, B., and Bortniak, J.: Seasonal variation in Antarctic
aerosol, J. Aerosol Sci., 12, 491–504, https://doi.org/10.1016/0021-8502(81)90052-5,
1981.
Peng, J., Hu, M., Guo, S., Du, Z., Shang, D., Zheng, J., Zheng, J., Zeng, L.,
Shao, M., Wu, Y., Collins, D., and Zhang, R.: Ageing and hygroscopicity
variation of black carbon particles in Beijing measured by a
quasi-atmospheric aerosol evolution study (QUALITY) chamber, Atmos. Chem.
Phys., 17, 10333–10348, https://doi.org/10.5194/acp-17-10333-2017, 2017.
Petters, M. D. and Kreidenweis, S. M.: A single parameter representation of
hygroscopic growth and cloud condensation nucleus activity, Atmos. Chem.
Phys., 7, 1961–1971, https://doi.org/10.5194/acp-7-1961-2007, 2007.
Polissar, A. V., Hopke, P. K., Paatero, P., Kaufmann, Y. J., Hall, D. K.,
Bodhaine, B. A., Dutton, E. G., and Harris, J. M.: The aerosol at Barrow,
Alaska: long-term trends and source locations, Atmos. Environ., 33,
2441–2458, https://doi.org/10.1016/s1352-2310(98)00423-3, 1999.
Price, D. J., Chen, C.-L., Russell, L. M., Lamjiri, M. A., Betha, R.,
Sanchez, K., Liu, J., Lee, A. K. Y., and Cocker, D. R.: More unsaturated,
cooking-type hydrocarbon-like organic aerosol particle emissions from
renewable diesel compared to ultra low sulfur diesel in at-sea operations of
a research vessel, Aerosol Sci. Tech., 51, 135–146,
https://doi.org/10.1080/02786826.2016.1238033, 2017.
Read, K. A., Lewis, A. C., Bauguitte, S., Rankin, A. M., Salmon, R. A.,
Wolff, E. W., Saiz-Lopez, A., Bloss, W. J., Heard, D. E., Lee, J. D., and
Plane, J. M. C.: DMS and MSA measurements in the Antarctic Boundary Layer:
impact of BrO on MSA production, Atmos. Chem. Phys., 8, 2985–2997,
https://doi.org/10.5194/acp-8-2985-2008, 2008.
Rickard, A. R., Wyche, K. P., Metzger, A., Monks, P. S., Ellis, A. M.,
Dommen, J., Baltensperger, U., Jenkin, M. E., and Pilling, M. J.: Gas phase
precursors to anthropogenic secondary organic aerosol Using the Master
Chemical Mechanism to probe detailed observations of 1,3,5-trimethylbenzene
photo-oxidation, Atmos. Environ., 44, 5423–5433,
https://doi.org/10.1016/j.atmosenv.2009.09.043, 2010.
Rickards, A. M. J., Miles, R. E. H., Davies, J. F., Marshall, F. H., and
Reid, J. P.: Measurements of the Sensitivity of Aerosol Hygroscopicity and
the kappa Parameter to the O ∕ C Ratio, J. Phys. Chem. A, 117,
14120–14131, https://doi.org/10.1021/jp407991n, 2013.
Riddick, S. N., Dragosits, U., Blackall, T. D., Daunt, F., Wanless, S., and
Sutton, M. A.: The global distribution of ammonia emissions from seabird
colonies, Atmos. Environ., 55, 319–327, https://doi.org/10.1016/j.atmosenv.2012.02.052,
2012.
Russell, L. M.: Aerosol organic-mass-to-organic-carbon ratio measurements,
Environ. Sci. Technol., 37, 2982–2987, 10.1021/es026123w, 2003.
Russell, L. M. and Shaw, G. E.: Arctic and Antarctic/Arctic Haze, in:
Encyclopedia of Atmospheric Sciences, 2nd Edn., edited by: North, G., Pyle,
J., and Zhang, F., Elsevier, UK and USA, 116–121, 2015.
Russell, L. M., Bahadur, R., Hawkins, L. N., Allan, J., Baumgardner, D.,
Quinn, P. K., and Bates, T. S.: Organic aerosol characterization by
complementary measurements of chemical bonds and molecular fragments, Atmos.
Environ., 43, 6100–6105, https://doi.org/10.1016/j.atmosenv.2009.09.036, 2009.
Russell, L. M., Hawkins, L. N., Frossard, A. A., Quinn, P. K., and Bates, T.
S.: Carbohydrate-like composition of submicron atmospheric particles and
their production from ocean bubble bursting, P. Natl. Acad. Sci. USA, 107,
6652–6657, https://doi.org/10.1073/pnas.0908905107, 2010.
Russell, L. M., Bahadur, R., and Ziemann, P. J.: Identifying organic aerosol
sources by comparing functional group composition in chamber and atmospheric
particles, P. Natl. Acad. Sci. USA, 108, 3516–3521,
https://doi.org/10.1073/pnas.1006461108, 2011.
Saliba, G., Saleh, R., Zhao, Y. L., Presto, A. A., Larnbe, A. T., Frodin, B.,
Sardar, S., Maldonado, H., Maddox, C., May, A. A., Drozd, G. T., Goldstein,
A. H., Russell, L. M., Hagen, F., and Robinson, A. L.: Comparison of Gasoline
Direct-Injection (GDI) and Port Fuel Injection (PFI) Vehicle Emissions:
Emission Certification Standards, Cold-Start, Secondary Organic Aerosol
Formation Potential, and Potential Climate Impacts, Environ. Sci. Technol.,
51, 6542–6552, https://doi.org/10.1021/acs.est.6b06509, 2017.
Savoie, D., Prospero, J., Larsen, R., Huang, F., Izaguirre, M., Huang, T.,
Snowdon, T., Custals, L., and Sanderson, C.: Nitrogen and sulfur species in
Antarctic aerosols at Mawson, Palmer station, and Marsh (King George Island),
J. Atmos. Chem., 17, 95–122, 1993.
Sax, M., Zenobi, R., Baltensperger, U., and Kalberer, M.: Time resolved
infrared spectroscopic analysis of aerosol formed by photo-oxidation of
1,3,5-trimethylbenzene and alpha-pinene, Aerosol Sci. Tech., 39, 822–830,
https://doi.org/10.1080/02786820500257859, 2005.
Saxena, V. and Ruggiero, F.: Aerosol measurements at Palmer Station,
Antarctica, Contributions to Antarctic Research, I, 1–5, 1990.
Scalabrin, E., Zangrando, R., Barbaro, E., Kehrwald, N. M., Gabrieli, J.,
Barbante, C., and Gambaro, A.: Amino acids in Arctic aerosols, Atmos. Chem.
Phys., 12, 10453–10463, https://doi.org/10.5194/acp-12-10453-2012, 2012.
Schmale, J., Schneider, J., Nemitz, E., Tang, Y. S., Dragosits, U., Blackall,
T. D., Trathan, P. N., Phillips, G. J., Sutton, M., and Braban, C. F.:
Sub-Antarctic marine aerosol: dominant contributions from biogenic sources,
Atmos. Chem. Phys., 13, 8669–8694, https://doi.org/10.5194/acp-13-8669-2013,
2013.
Schmidt, R. A.: Estimates of threshold windspeed from particle sizes in
blowing snow, Cold Reg. Sci. Technol., 4, 187–193,
https://doi.org/10.1016/0165-232x(81)90003-3, 1981.
Shaw, P. M., Russell, L. M., Jefferson, A., and Quinn, P. K.: Arctic organic
aerosol measurements show particles from mixed combustion in spring haze and
from frost flowers in winter, Geophys. Res. Lett., 37, L10803,
https://doi.org/10.1029/2010gl042831, 2010.
Shi, J. H., Gao, H. W., Qi, J. H., Zhang, J., and Yao, X. H.: Sources,
compositions, and distributions of water-soluble organic nitrogen in aerosols
over the China Sea, J. Geophys. Res.-Atmos., 115, D17303,
https://doi.org/10.1029/2009jd013238, 2010.
Solomon, S., Sanders, R. W., Jakoubek, R. O., Arpag, K. H., Stephens, S. L.,
Keys, J. G., and Garcia, R. R.: Visible and near-ultraviolet spectroscopy at
McMurdo-station, Antarctica. 10. Reductions of stratospheric NO2 Due
to Pinatubo aerosols, J. Geophys. Res.-Atmos., 99, 3509–3516,
https://doi.org/10.1029/93jd03088, 1994.
Steig, E. J., Schneider, D. P., Rutherford, S. D., Mann, M. E., Comiso, J.
C., and Shindell, D. T.: Warming of the Antarctic ice-sheet surface since the
1957 International Geophysical Year, Nature, 457, 459–462,
https://doi.org/10.1038/nature07669, 2009.
Stephanou, E. G. and Stratigakis, N.: Oxocarboxylic and α,
ω-dicarboxylic acids: photooxidation products of biogenic unsaturated
fatty acids present in urban aerosols, Environ. Sci. Technol., 27,
1403–1407, 1993.
Stohl, A.: Characteristics of atmospheric transport into the Arctic
troposphere, J. Geophys. Res.-Atmos., 111, D11306, https://doi.org/10.1029/2005jd006888,
2006.
Stohl, A. and Sodemann, H.: Characteristics of atmospheric transport into the
Antarctic troposphere, J. Geophys. Res.-Atmos., 115, D02305,
https://doi.org/10.1029/2009jd012536, 2010.
Su, H., Rose, D., Cheng, Y. F., Gunthe, S. S., Massling, A., Stock, M.,
Wiedensohler, A., Andreae, M. O., and Pöschl, U.: Hygroscopicity
distribution concept for measurement data analysis and modeling of aerosol
particle mixing state with regard to hygroscopic growth and CCN activation,
Atmos. Chem. Phys., 10, 7489–7503, https://doi.org/10.5194/acp-10-7489-2010,
2010.
Takahama, S., Johnson, A., and Russell, L. M.: Quantification of carboxylic
and carbonyl functional groups in organic aerosol infrared absorbance
spectra, Aerosol Sci. Tech., 47, 310–325, https://doi.org/10.1080/02786826.2012.752065,
2013.
Thomas, D. N. and Dieckmann, G. S.: Sea ice: an introduction to its physics,
chemistry, biology and geology, John Wiley & Sons, 2008.
Tukey, J. W.: Exploratory Data Analysis, 1st Edn., Behavioral Science,
Addison-Wesley, Reading, MA, 1977.
Udisti, R., Dayan, U., Becagli, S., Busetto, M., Frosini, D., Legrand, M.,
Lucarelli, F., Preunkert, S., Severi, M., Traversi, R., and Vitale, V.: Sea
spray aerosol in central Antarctica. Present atmospheric behaviour and
implications for paleoclimatic reconstructions, Atmos. Environ., 52,
109–120, https://doi.org/10.1016/j.atmosenv.2011.10.018, 2012.
Usher, C. R., Michel, A. E., and Grassian, V. H.: Reactions on mineral dust,
Chem. Rev., 103, 4883–4939, https://doi.org/10.1021/cr020657y, 2003.
Velleman, P. F.: Robust nonlinear data smoothers – definitions and
recommendations, P. Natl. Acad. Sci. USA, 74, 434–436,
https://doi.org/10.1073/pnas.74.2.434, 1977.
Violaki, K., Zarbas, P., and Mihalopoulos, N.: Long-term measurements of
dissolved organic nitrogen (DON) in atmospheric deposition in the Eastern
Mediterranean: Fluxes, origin and biogeochemical implications, Mar. Chem.,
120, 179–186, https://doi.org/10.1016/j.marchem.2009.08.004, 2010.
Vu, D., Short, D., Karavalakis, G., Durbin, T. D., and Asa-Awuku, A.: Will
Aerosol Hygroscopicity Change with Biodiesel, Renewable Diesel Fuels and
Emission Control Technologies?, Environ. Sci. Technol., 51, 1580–1586,
https://doi.org/10.1021/acs.est.6b03908, 2017.
Wagenbach, D., Ducroz, F., Mulvaney, R., Keck, L., Minikin, A., Legrand, M.,
Hall, J. S., and Wolff, E. W.: Sea-salt aerosol in coastal Antarctic regions,
J. Geophys. Res.-Atmos., 103, 10961–10974, https://doi.org/10.1029/97jd01804, 1998.
Warburton, J. A.: Surface measurements of Aitken nuclei at McMurdo, Siple,
Byrd, and South-pole stations, Antarct. J. US, 8, 236–236, 1973.
Weber, R. J., McMurry, P. H., Mauldin, L., Tanner, D. J., Eisele, F. L.,
Brechtel, F. J., Kreidenweis, S. M., Kok, G. L., Schillawski, R. D., and
Baumgardner, D.: A study of new particle formation and growth involving
biogenic and trace gas species measured during ACE 1, J. Geophys.
Res.-Atmos., 103, 16385–16396, https://doi.org/10.1029/97jd02465, 1998.
Wedyan, M. A. and Preston, M. R.: The coupling of surface seawater organic
nitrogen and the marine aerosol as inferred from enantiomer-specific amino
acid analysis, Atmos. Environ., 42, 8698–8705,
https://doi.org/10.1016/j.atmosenv.2008.04.038, 2008.
Weller, R. and Wagenbach, D.: Year-round chemical aerosol records in
continental Antarctica obtained by automatic samplings, Tellus B, 59,
755–765, https://doi.org/10.1111/j.1600-0889.2007.00293.x, 2007.
Weller, R., Minikin, A., Petzold, A., Wagenbach, D., and König-Langlo,
G.: Characterization of long-term and seasonal variations of black carbon
(BC) concentrations at Neumayer, Antarctica, Atmos. Chem. Phys., 13,
1579–1590, https://doi.org/10.5194/acp-13-1579-2013, 2013.
Wex, H., McFiggans, G., Henning, S., and Stratmann, F.: Influence of the
external mixing state of atmospheric aerosol on derived CCN number
concentrations, Geophys. Res. Lett., 37, L10805, https://doi.org/10.1029/2010gl043337,
2010.
Wyche, K. P., Monks, P. S., Ellis, A. M., Cordell, R. L., Parker, A. E.,
Whyte, C., Metzger, A., Dommen, J., Duplissy, J., Prevot, A. S. H.,
Baltensperger, U., Rickard, A. R., and Wulfert, F.: Gas phase precursors to
anthropogenic secondary organic aerosol: detailed observations of
1,3,5-trimethylbenzene photooxidation, Atmos. Chem. Phys., 9, 635–665,
https://doi.org/10.5194/acp-9-635-2009, 2009.
Xu, G. J., Gao, Y., Lin, Q., Li, W., and Chen, L. Q.: Characteristics of
water-soluble inorganic and organic ions in aerosols over the Southern Ocean
and coastal East Antarctica during austral summer, J. Geophys. Res.-Atmos.,
118, 13303–13318, https://doi.org/10.1002/2013jd019496, 2013.
Yang, X., Pyle, J. A., and Cox, R. A.: Sea salt aerosol production and
bromine release: Role of snow on sea ice, Geophys. Res. Lett., 35, L16815,
https://doi.org/10.1029/2008gl034536, 2008.
Zangrando, R., Barbaro, E., Vecchiato, M., Kehrwald, N. M., Barbante, C., and
Gambaro, A.: Levoglucosan and phenols in Antarctic marine, coastal and
plateau aerosols, Sci. Total Environ., 544, 606–616,
https://doi.org/10.1016/j.scitotenv.2015.11.166, 2016.
Short summary
Observations of the organic components of the natural aerosol are scarce in Antarctica, which limits our understanding of natural aerosols and their connection to cloud albedo. We took yearlong measurements of organic aerosols at McMurdo Station. The natural organic aerosol was 150 times higher in summer than in winter. We showed the natural sources of OM were characterized by amide, which may be from seabird populations. Acid was high in summer and likely formed by secondary reactions.
Observations of the organic components of the natural aerosol are scarce in Antarctica, which...
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