Articles | Volume 18, issue 22
https://doi.org/10.5194/acp-18-16689-2018
© 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-18-16689-2018
© Author(s) 2018. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
The importance of blowing snow to halogen-containing aerosol in coastal Antarctica: influence of source region versus wind speed
Michael R. Giordano
Department of Civil, Architectural, and Environmental Engineering,
Drexel University, Philadelphia, Pennsylvania, USA
Lars E. Kalnajs
Laboratory for Atmospheric and Space Physics, University of Colorado
at Boulder, Boulder, Colorado, USA
J. Douglas Goetz
Department of Civil, Architectural, and Environmental Engineering,
Drexel University, Philadelphia, Pennsylvania, USA
now at: Laboratory for Atmospheric and Space Physics, University of
Colorado at Boulder, Boulder, Colorado, USA
Anita M. Avery
Department of Civil, Architectural, and Environmental Engineering,
Drexel University, Philadelphia, Pennsylvania, USA
now at: Aerodyne Research, Inc., Billerica, Massachusetts, USA
Erin Katz
Department of Chemistry, Drexel University, Philadelphia,
Pennsylvania, USA
Nathaniel W. May
Department of Chemistry, University of Michigan, Ann Arbor, Michigan,
USA
Anna Leemon
Department of Chemistry, University of Michigan, Ann Arbor, Michigan,
USA
Claire Mattson
Department of Chemistry, University of Michigan, Ann Arbor, Michigan,
USA
Kerri A. Pratt
Department of Chemistry, University of Michigan, Ann Arbor, Michigan,
USA
Department of Civil, Architectural, and Environmental Engineering,
Drexel University, Philadelphia, Pennsylvania, USA
Department of Chemistry, Drexel University, Philadelphia,
Pennsylvania, USA
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Atmos. Chem. Phys., 18, 14653–14679, https://doi.org/10.5194/acp-18-14653-2018, https://doi.org/10.5194/acp-18-14653-2018, 2018
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Size distributions and emission factors of submicron aerosol were quantified using online techniques for a variety of common but under-sampled combustion sources in South Asia: wood and dung cooking fires, groundwater pumps, brick kilns, trash burning, and open burning of crop residues. Optical properties (brown carbon light absorption and the absorption Ångström exponent, AAE) of the emissions were also investigated. Contextual comparisons to the literature and other NAMaSTE results were made.
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The 100-year GWP is the most widely used metric for comparing the climate impact of different gases such as methane and carbon dioxide. However, there have been recent arguments for the use of different timescales. This paper uses straightforward estimates of future damages to quantitatively determine the appropriate timescale as a function of how society discounts the future and finds that the 100-year timescale is consistent with commonly used discount rates.
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Atmos. Chem. Phys., 17, 1–20, https://doi.org/10.5194/acp-17-1-2017, https://doi.org/10.5194/acp-17-1-2017, 2017
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This paper summarizes two field measurements of particles and gases made in coastal Antarctica and represents the first real-time composition measurements of particles in this understudied area of the world. Using the combined data from both field measurements, we find that there is a constant background of particles in coastal Antarctica and that they are mostly sulfate. Seasonal transitions from winter to spring add additional particles, and that from spring to summer adds additional sulfate.
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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, Tiaa Laurila, Vaios Moschos, Tuukka Petäjä, Kerri A. Pratt, Lauriane L. J. Quéléver, Matthew D. Shupe, Paul Zieger, Tuija Jokinen, and Julia Schmale
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This preprint is open for discussion and under review for Atmospheric Chemistry and Physics (ACP).
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Natalie Brett, Kathy S. Law, Steve R. Arnold, Javier G. Fochesatto, Jean-Christophe Raut, Tatsuo Onishi, Robert Gilliam, Kathleen Fahey, Deanna Huff, George Pouliot, Brice Barret, Elsa Dieudonne, Roman Pohorsky, Julia Schmale, Andrea Baccarini, Slimane Bekki, Gianluca Pappaccogli, Federico Scoto, Stefano Decesari, Antonio Donateo, Meeta Cesler-Maloney, William Simpson, Patrice Medina, Barbara D'Anna, Brice Temime-Roussel, Joel Savarino, Sarah Albertin, Jingqiu Mao, Becky Alexander, Allison Moon, Peter F. DeCarlo, Vanessa Selimovic, Robert Yokelson, and Ellis S. Robinson
EGUsphere, https://doi.org/10.5194/egusphere-2024-1450, https://doi.org/10.5194/egusphere-2024-1450, 2024
This preprint is open for discussion and under review for Atmospheric Chemistry and Physics (ACP).
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Processes influencing dispersion of local anthropogenic emissions in Arctic wintertime are investigated with dispersion model simulations. Modelled power plant plume rise that considers surface and elevated temperature inversions improves results compared to observations. Modelled near-surface concentrations are improved by representation of vertical mixing and emission estimates. Large increases in diesel vehicle emissions at temperatures reaching -35 °C are required to reproduce observed NOx.
Mahen Konwar, Benjamin Werden, Edward C. Fortner, Sudarsan Bera, Mercy Varghese, Subharthi Chowdhuri, Kurt Hibert, Philip Croteau, John Jayne, Manjula Canagaratna, Neelam Malap, Sandeep Jayakumar, Shivsai A. Dixit, Palani Murugavel, Duncan Axisa, Darrel Baumgardner, Peter F. DeCarlo, Doug R. Worsnop, and Thara Prabhakaran
Atmos. Meas. Tech., 17, 2387–2400, https://doi.org/10.5194/amt-17-2387-2024, https://doi.org/10.5194/amt-17-2387-2024, 2024
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In a warm cloud seeding experiment hygroscopic particles are released to alter cloud processes to induce early raindrops. During the Cloud–Aerosol Interaction and Precipitation Enhancement Experiment, airborne mini aerosol mass spectrometers analyse the particles on which clouds form. The seeded clouds showed higher concentrations of chlorine and potassium, the oxidizing agents of flares. Small cloud droplet concentrations increased, and seeding particles were detected in deep cloud depths.
Emily Wein, Lars Kalnajs, and Darin Toohey
Atmos. Meas. Tech. Discuss., https://doi.org/10.5194/amt-2024-34, https://doi.org/10.5194/amt-2024-34, 2024
Preprint under review for AMT
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We describe a low cost and small research grade spectrometer for measurements of water vapor in the boundary layer. The instrument uses small Arduino microcontrollers and inexpensive laser diodes to reduce cost while maintaining high performance comparable to more expensive instruments. Performance was assessed with intercomparisons between commercially available instruments outdoors. The design's simplicity, performance and price point allow it to be accessible to a variety of users.
Nathaniel Brockway, Peter K. Peterson, Katja Bigge, Kristian D. Hajny, Paul B. Shepson, Kerri A. Pratt, Jose D. Fuentes, Tim Starn, Robert Kaeser, Brian H. Stirm, and William R. Simpson
Atmos. Chem. Phys., 24, 23–40, https://doi.org/10.5194/acp-24-23-2024, https://doi.org/10.5194/acp-24-23-2024, 2024
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Bromine monoxide (BrO) strongly affects atmospheric chemistry in the springtime Arctic, yet there are still many uncertainties around its sources and recycling, particularly in the context of a rapidly changing Arctic. In this study, we observed BrO as a function of altitude above the Alaskan Arctic. We found that BrO was often most concentrated near the ground, confirming the ability of snow to produce and recycle reactive bromine, and identified four common vertical distributions of BrO.
Eleftherios Ioannidis, Kathy S. Law, Jean-Christophe Raut, Louis Marelle, Tatsuo Onishi, Rachel M. Kirpes, Lucia M. Upchurch, Thomas Tuch, Alfred Wiedensohler, Andreas Massling, Henrik Skov, Patricia K. Quinn, and Kerri A. Pratt
Atmos. Chem. Phys., 23, 5641–5678, https://doi.org/10.5194/acp-23-5641-2023, https://doi.org/10.5194/acp-23-5641-2023, 2023
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Remote and local anthropogenic emissions contribute to wintertime Arctic haze, with enhanced aerosol concentrations, but natural sources, which also contribute, are less well studied. Here, modelled wintertime sea-spray aerosols are improved in WRF-Chem over the wider Arctic by including updated wind speed and temperature-dependent treatments. As a result, anthropogenic nitrate aerosols are also improved. Open leads are confirmed to be the main source of sea-spray aerosols over northern Alaska.
J. Douglas Goetz, Lars E. Kalnajs, Terry Deshler, Sean M. Davis, Martina Bramberger, and M. Joan Alexander
Atmos. Meas. Tech., 16, 791–807, https://doi.org/10.5194/amt-16-791-2023, https://doi.org/10.5194/amt-16-791-2023, 2023
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An instrument for in situ continuous 2 km vertical profiles of temperature below high-altitude balloons was developed for high-temporal-resolution measurements within the upper troposphere and lower stratosphere using fiber-optic distributed temperature sensing. The mechanical, electrical, and temperature calibration systems were validated from a short mid-latitude constant-altitude balloon flight within the lower stratosphere. The instrument observed small-scale and inertial gravity waves.
Qianjie Chen, Jessica A. Mirrielees, Sham Thanekar, Nicole A. Loeb, Rachel M. Kirpes, Lucia M. Upchurch, Anna J. Barget, Nurun Nahar Lata, Angela R. W. Raso, Stephen M. McNamara, Swarup China, Patricia K. Quinn, Andrew P. Ault, Aaron Kennedy, Paul B. Shepson, Jose D. Fuentes, and Kerri A. Pratt
Atmos. Chem. Phys., 22, 15263–15285, https://doi.org/10.5194/acp-22-15263-2022, https://doi.org/10.5194/acp-22-15263-2022, 2022
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During a spring field campaign in the coastal Arctic, ultrafine particles were enhanced during high wind speeds, and coarse-mode particles were reduced during blowing snow. Calculated periods blowing snow were overpredicted compared to observations. Sea spray aerosols produced by sea ice leads affected the composition of aerosols and snowpack. An improved understanding of aerosol emissions from leads and blowing snow is critical for predicting the future climate of the rapidly warming Arctic.
Kathryn D. Kulju, Stephen M. McNamara, Qianjie Chen, Hannah S. Kenagy, Jacinta Edebeli, Jose D. Fuentes, Steven B. Bertman, and Kerri A. Pratt
Atmos. Chem. Phys., 22, 2553–2568, https://doi.org/10.5194/acp-22-2553-2022, https://doi.org/10.5194/acp-22-2553-2022, 2022
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N2O5 uptake by chloride-containing surfaces produces ClNO2, which photolyzes, producing NO2 and highly reactive Cl radicals that impact air quality. In the inland urban atmosphere, ClNO2 was elevated during lower air turbulence and over snow-covered ground, from snowpack ClNO2 production. N2O5 and ClNO2 levels were lowest, on average, during rainfall and fog because of scavenging, with N2O5 scavenging by fog droplets likely contributing to observed increased particulate nitrate concentrations.
Dandan Wei, Hariprasad D. Alwe, Dylan B. Millet, Brandon Bottorff, Michelle Lew, Philip S. Stevens, Joshua D. Shutter, Joshua L. Cox, Frank N. Keutsch, Qianwen Shi, Sarah C. Kavassalis, Jennifer G. Murphy, Krystal T. Vasquez, Hannah M. Allen, Eric Praske, John D. Crounse, Paul O. Wennberg, Paul B. Shepson, Alexander A. T. Bui, Henry W. Wallace, Robert J. Griffin, Nathaniel W. May, Megan Connor, Jonathan H. Slade, Kerri A. Pratt, Ezra C. Wood, Mathew Rollings, Benjamin L. Deming, Daniel C. Anderson, and Allison L. Steiner
Geosci. Model Dev., 14, 6309–6329, https://doi.org/10.5194/gmd-14-6309-2021, https://doi.org/10.5194/gmd-14-6309-2021, 2021
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Over the past decade, understanding of isoprene oxidation has improved, and proper representation of isoprene oxidation and isoprene-derived SOA (iSOA) formation in canopy–chemistry models is now recognized to be important for an accurate understanding of forest–atmosphere exchange. The updated FORCAsT version 2.0 improves the estimation of some isoprene oxidation products and is one of the few canopy models currently capable of simulating SOA formation from monoterpenes and isoprene.
Benjamin A. Nault, Duseong S. Jo, Brian C. McDonald, Pedro Campuzano-Jost, Douglas A. Day, Weiwei Hu, Jason C. Schroder, James Allan, Donald R. Blake, Manjula R. Canagaratna, Hugh Coe, Matthew M. Coggon, Peter F. DeCarlo, Glenn S. Diskin, Rachel Dunmore, Frank Flocke, Alan Fried, Jessica B. Gilman, Georgios Gkatzelis, Jacqui F. Hamilton, Thomas F. Hanisco, Patrick L. Hayes, Daven K. Henze, Alma Hodzic, James Hopkins, Min Hu, L. Greggory Huey, B. Thomas Jobson, William C. Kuster, Alastair Lewis, Meng Li, Jin Liao, M. Omar Nawaz, Ilana B. Pollack, Jeffrey Peischl, Bernhard Rappenglück, Claire E. Reeves, Dirk Richter, James M. Roberts, Thomas B. Ryerson, Min Shao, Jacob M. Sommers, James Walega, Carsten Warneke, Petter Weibring, Glenn M. Wolfe, Dominique E. Young, Bin Yuan, Qiang Zhang, Joost A. de Gouw, and Jose L. Jimenez
Atmos. Chem. Phys., 21, 11201–11224, https://doi.org/10.5194/acp-21-11201-2021, https://doi.org/10.5194/acp-21-11201-2021, 2021
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Secondary organic aerosol (SOA) is an important aspect of poor air quality for urban regions around the world, where a large fraction of the population lives. However, there is still large uncertainty in predicting SOA in urban regions. Here, we used data from 11 urban campaigns and show that the variability in SOA production in these regions is predictable and is explained by key emissions. These results are used to estimate the premature mortality associated with SOA in urban regions.
Lars E. Kalnajs, Sean M. Davis, J. Douglas Goetz, Terry Deshler, Sergey Khaykin, Alex St. Clair, Albert Hertzog, Jerome Bordereau, and Alexey Lykov
Atmos. Meas. Tech., 14, 2635–2648, https://doi.org/10.5194/amt-14-2635-2021, https://doi.org/10.5194/amt-14-2635-2021, 2021
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This work introduces a novel instrument system for high-resolution atmospheric profiling, which lowers and retracts a suspended instrument package beneath drifting long-duration balloons. During a 100 d circumtropical flight, the instrument collected over a hundred 2 km profiles of temperature, water vapor, clouds, and aerosol at 1 m resolution, yielding unprecedented geographic sampling and vertical resolution measurements of the tropical tropopause layer.
Md. Robiul Islam, Thilina Jayarathne, Isobel J. Simpson, Benjamin Werden, John Maben, Ashley Gilbert, Puppala S. Praveen, Sagar Adhikari, Arnico K. Panday, Maheswar Rupakheti, Donald R. Blake, Robert J. Yokelson, Peter F. DeCarlo, William C. Keene, and Elizabeth A. Stone
Atmos. Chem. Phys., 20, 2927–2951, https://doi.org/10.5194/acp-20-2927-2020, https://doi.org/10.5194/acp-20-2927-2020, 2020
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The Kathmandu Valley experiences high levels of air pollution. In this study, atmospheric gases and particulate matter were characterized by online and off-line measurements, with an emphasis on understanding their sources. The major sources of particulate matter and trace gases were identified as garbage burning, biomass burning, and vehicles. The majority of secondary organic aerosol was attributed to anthropogenic precursors, while a minority was attributed to biogenic gases.
John W. Halfacre, Paul B. Shepson, and Kerri A. Pratt
Atmos. Chem. Phys., 19, 4917–4931, https://doi.org/10.5194/acp-19-4917-2019, https://doi.org/10.5194/acp-19-4917-2019, 2019
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In this study, we found that a chemical called hydroxyl radical can help create chlorine, bromine, and iodine (i.e., halogens) from acidic frozen imitation seawater. Even more halogens are created if we also add ozone. This result helps our understanding of how halogens are released from the frozen Arctic ice and snow into the atmosphere, where they alter the atmosphere's oxidation ability.
Jessie M. Creamean, Rachel M. Kirpes, Kerri A. Pratt, Nicholas J. Spada, Maximilian Maahn, Gijs de Boer, Russell C. Schnell, and Swarup China
Atmos. Chem. Phys., 18, 18023–18042, https://doi.org/10.5194/acp-18-18023-2018, https://doi.org/10.5194/acp-18-18023-2018, 2018
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Warm-temperature ice nucleating particles (INPs) were observed during a springtime transition period of the melting of frozen surfaces in Northern Alaska. Such INPs were likely biological and from marine and terrestrial (tundra) sources. Influxes of these efficient INPs may have important implications for Arctic cloud ice formation and, consequently, the surface energy budget.
J. Douglas Goetz, Michael R. Giordano, Chelsea E. Stockwell, Ted J. Christian, Rashmi Maharjan, Sagar Adhikari, Prakash V. Bhave, Puppala S. Praveen, Arnico K. Panday, Thilina Jayarathne, Elizabeth A. Stone, Robert J. Yokelson, and Peter F. DeCarlo
Atmos. Chem. Phys., 18, 14653–14679, https://doi.org/10.5194/acp-18-14653-2018, https://doi.org/10.5194/acp-18-14653-2018, 2018
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Size distributions and emission factors of submicron aerosol were quantified using online techniques for a variety of common but under-sampled combustion sources in South Asia: wood and dung cooking fires, groundwater pumps, brick kilns, trash burning, and open burning of crop residues. Optical properties (brown carbon light absorption and the absorption Ångström exponent, AAE) of the emissions were also investigated. Contextual comparisons to the literature and other NAMaSTE results were made.
Marcus C. Sarofim and Michael R. Giordano
Earth Syst. Dynam., 9, 1013–1024, https://doi.org/10.5194/esd-9-1013-2018, https://doi.org/10.5194/esd-9-1013-2018, 2018
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The 100-year GWP is the most widely used metric for comparing the climate impact of different gases such as methane and carbon dioxide. However, there have been recent arguments for the use of different timescales. This paper uses straightforward estimates of future damages to quantitatively determine the appropriate timescale as a function of how society discounts the future and finds that the 100-year timescale is consistent with commonly used discount rates.
Rachel M. Kirpes, Amy L. Bondy, Daniel Bonanno, Ryan C. Moffet, Bingbing Wang, Alexander Laskin, Andrew P. Ault, and Kerri A. Pratt
Atmos. Chem. Phys., 18, 3937–3949, https://doi.org/10.5194/acp-18-3937-2018, https://doi.org/10.5194/acp-18-3937-2018, 2018
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Arctic atmospheric particles have important climate impacts via cloud formation and precipitation, particularly in the wintertime. We show that sulfate, formed during atmospheric transport, is within individual sea spray particles and organic particles measured in the Alaskan Arctic. Greater contributions of combustion emissions were observed when the wind direction came from the Prudhoe Bay oil fields, showing its regional influence.
Matthew J. Gunsch, Nathaniel W. May, Miao Wen, Courtney L. H. Bottenus, Daniel J. Gardner, Timothy M. VanReken, Steven B. Bertman, Philip K. Hopke, Andrew P. Ault, and Kerri A. Pratt
Atmos. Chem. Phys., 18, 3701–3715, https://doi.org/10.5194/acp-18-3701-2018, https://doi.org/10.5194/acp-18-3701-2018, 2018
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During summer 2014, atmospheric particulate matter in northern Michigan was impacted by wildfire emissions under all air mass conditions (Canadian wildfires, US urban, and Canadian forest influences). Biomass burning particles coated with secondary organic aerosol contributed the majority of the submicron aerosol mass. Given increasing wildfires, the impacts of biomass burning on air quality must be assessed, particularly for downwind areas impacted by long-range transport.
Thilina Jayarathne, Chelsea E. Stockwell, Prakash V. Bhave, Puppala S. Praveen, Chathurika M. Rathnayake, Md. Robiul Islam, Arnico K. Panday, Sagar Adhikari, Rashmi Maharjan, J. Douglas Goetz, Peter F. DeCarlo, Eri Saikawa, Robert J. Yokelson, and Elizabeth A. Stone
Atmos. Chem. Phys., 18, 2259–2286, https://doi.org/10.5194/acp-18-2259-2018, https://doi.org/10.5194/acp-18-2259-2018, 2018
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Emissions of fine particulate matter and its constituents were quantified for a variety of under-sampled combustion sources in South Asia: wood and dung cooking fires, generators, groundwater pumps, brick kilns, trash burning, and open burning of biomasses. Garbage burning and three-stone cooking fires were among the highest emitters, while servicing of motor vehicles significantly reduced PM. These data may be used in source apportionment and to update regional and global emission inventories.
Ryan D. Cook, Ying-Hsuan Lin, Zhuoyu Peng, Eric Boone, Rosalie K. Chu, James E. Dukett, Matthew J. Gunsch, Wuliang Zhang, Nikola Tolic, Alexander Laskin, and Kerri A. Pratt
Atmos. Chem. Phys., 17, 15167–15180, https://doi.org/10.5194/acp-17-15167-2017, https://doi.org/10.5194/acp-17-15167-2017, 2017
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Reactions occur within water in both atmospheric particles and cloud droplets, yet little is known about the organic compounds in cloud water. In this work, cloud water samples were collected at Whiteface Mountain, New York, and analyzed using ultra-high-resolution mass spectrometry to investigate the molecular composition of the dissolved organic compounds. The results focus on changes in cloud water composition with air mass origin – influences of forest, urban, and wildfire emissions.
Matthew J. Gunsch, Rachel M. Kirpes, Katheryn R. Kolesar, Tate E. Barrett, Swarup China, Rebecca J. Sheesley, Alexander Laskin, Alfred Wiedensohler, Thomas Tuch, and Kerri A. Pratt
Atmos. Chem. Phys., 17, 10879–10892, https://doi.org/10.5194/acp-17-10879-2017, https://doi.org/10.5194/acp-17-10879-2017, 2017
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Arctic sea ice loss is leading to increasing petroleum extraction and shipping. It is necessary to identify emissions from these activities for improved Arctic air quality and climate assessment. Atmospheric particles were measured from August to September 2015 in Utqiaġvik, AK. For periods influenced by Prudhoe Bay, significant influence associated with combustion emissions was observed, compared to fresh sea spray influence during Arctic Ocean periods.
William R. Simpson, Peter K. Peterson, Udo Frieß, Holger Sihler, Johannes Lampel, Ulrich Platt, Chris Moore, Kerri Pratt, Paul Shepson, John Halfacre, and Son V. Nghiem
Atmos. Chem. Phys., 17, 9291–9309, https://doi.org/10.5194/acp-17-9291-2017, https://doi.org/10.5194/acp-17-9291-2017, 2017
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We investigated Arctic atmospheric bromine chemistry during March–April 2012 to improve understanding of the role of sea ice and cracks in sea ice (leads) in this phenomenon. We find that leads vertically redistribute reactive bromine but that open/re-freezing leads are not major direct reactive halogen sources. Surface ozone depletion affects the vertical distribution and amount of reactive halogens, and aerosol particles are necessary but not sufficient to maintain reactive bromine aloft.
Peter K. Peterson, Denis Pöhler, Holger Sihler, Johannes Zielcke, Stephan General, Udo Frieß, Ulrich Platt, William R. Simpson, Son V. Nghiem, Paul B. Shepson, Brian H. Stirm, Suresh Dhaniyala, Thomas Wagner, Dana R. Caulton, Jose D. Fuentes, and Kerri A. Pratt
Atmos. Chem. Phys., 17, 7567–7579, https://doi.org/10.5194/acp-17-7567-2017, https://doi.org/10.5194/acp-17-7567-2017, 2017
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High-spatial-resolution aircraft measurements in the Arctic showed the sustained transport of reactive bromine in a lofted layer via heterogeneous reactions on aerosol particles. This process provides an explanation for free tropospheric reactive bromine and the significant spatial extent of satellite-observed bromine monoxide. The knowledge gained herein improves our understanding of the fate and transport of atmospheric pollutants in the Arctic.
Michael R. Giordano, Lars E. Kalnajs, Anita Avery, J. Douglas Goetz, Sean M. Davis, and Peter F. DeCarlo
Atmos. Chem. Phys., 17, 1–20, https://doi.org/10.5194/acp-17-1-2017, https://doi.org/10.5194/acp-17-1-2017, 2017
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This paper summarizes two field measurements of particles and gases made in coastal Antarctica and represents the first real-time composition measurements of particles in this understudied area of the world. Using the combined data from both field measurements, we find that there is a constant background of particles in coastal Antarctica and that they are mostly sulfate. Seasonal transitions from winter to spring add additional particles, and that from spring to summer adds additional sulfate.
Chelsea E. Stockwell, Ted J. Christian, J. Douglas Goetz, Thilina Jayarathne, Prakash V. Bhave, Puppala S. Praveen, Sagar Adhikari, Rashmi Maharjan, Peter F. DeCarlo, Elizabeth A. Stone, Eri Saikawa, Donald R. Blake, Isobel J. Simpson, Robert J. Yokelson, and Arnico K. Panday
Atmos. Chem. Phys., 16, 11043–11081, https://doi.org/10.5194/acp-16-11043-2016, https://doi.org/10.5194/acp-16-11043-2016, 2016
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We present the first, or rare, field measurements in South Asia of emission factors for up to 80 gases (pollutants, greenhouse gases, and precursors) and black carbon and aerosol optical properties at 405 and 870 nm for many previously under-sampled sources that are important in developing countries such as cooking with dung and wood, garbage and crop residue burning, brick kilns, motorcycles, generators and pumps, etc. Brown carbon contributes significantly to total aerosol absorption.
Nathaniel W. May, Jessica L. Axson, Alexa Watson, Kerri A. Pratt, and Andrew P. Ault
Atmos. Meas. Tech., 9, 4311–4325, https://doi.org/10.5194/amt-9-4311-2016, https://doi.org/10.5194/amt-9-4311-2016, 2016
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Aerosols are generated every time a wave breaks, as bubbles are formed that rise to the surface and burst. A great deal is known about sea spray aerosol from oceans, but very little is known about particles formed from freshwater, such as lakes and rivers. This study determines how "lake spray aerosol" is formed, which leads to distinctly different sizes and chemical composition from sea spray aerosol. These differences impact climate, weather, and human health near bodies of freshwater.
F. Xiong, K. M. McAvey, K. A. Pratt, C. J. Groff, M. A. Hostetler, M. A. Lipton, T. K. Starn, J. V. Seeley, S. B. Bertman, A. P. Teng, J. D. Crounse, T. B. Nguyen, P. O. Wennberg, P. K. Misztal, A. H. Goldstein, A. B. Guenther, A. R. Koss, K. F. Olson, J. A. de Gouw, K. Baumann, E. S. Edgerton, P. A. Feiner, L. Zhang, D. O. Miller, W. H. Brune, and P. B. Shepson
Atmos. Chem. Phys., 15, 11257–11272, https://doi.org/10.5194/acp-15-11257-2015, https://doi.org/10.5194/acp-15-11257-2015, 2015
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Hydroxynitrates from isoprene oxidation were quantified both in the laboratory and through field studies. The yield of hydroxynitrates 9(+4/-3)% derived from chamber experiments was applied in a zero-dimensional model to simulate the production and loss of isoprene hydroxynitrates in an ambient environment during the 2013 Southern Oxidant and Aerosol Study (SOAS). NOx was determined to be the limiting factor for the formation of isoprene hydroxynitrates during SOAS.
K. D. Custard, C. R. Thompson, K. A. Pratt, P B. Shepson, J. Liao, L. G. Huey, J. J. Orlando, A. J. Weinheimer, E. Apel, S. R. Hall, F. Flocke, L. Mauldin, R. S. Hornbrook, D. Pöhler, S. General, J. Zielcke, W. R. Simpson, U. Platt, A. Fried, P. Weibring, B. C. Sive, K. Ullmann, C. Cantrell, D. J. Knapp, and D. D. Montzka
Atmos. Chem. Phys., 15, 10799–10809, https://doi.org/10.5194/acp-15-10799-2015, https://doi.org/10.5194/acp-15-10799-2015, 2015
P. K. Peterson, W. R. Simpson, K. A. Pratt, P. B. Shepson, U. Frieß, J. Zielcke, U. Platt, S. J. Walsh, and S. V. Nghiem
Atmos. Chem. Phys., 15, 2119–2137, https://doi.org/10.5194/acp-15-2119-2015, https://doi.org/10.5194/acp-15-2119-2015, 2015
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We developed methods to measure the vertical distribution of bromine monoxide, a gas that oxidizes pollutants, above sea ice based upon MAX-DOAS observations from Barrow, Alaska, and find that atmospheric stability exerts a strong control on BrO's vertical distribution. Specifically, more stable (temperature inversion) situations result in BrO being closer to the ground while more neutral (not inverted) atmospheres allow BrO to ascend further aloft and grow to larger column abundance.
M. Giordano, C. Espinoza, and A. Asa-Awuku
Atmos. Chem. Phys., 15, 1807–1821, https://doi.org/10.5194/acp-15-1807-2015, https://doi.org/10.5194/acp-15-1807-2015, 2015
R. Chirico, M. Clairotte, T. W. Adam, B. Giechaskiel, M. F. Heringa, M. Elsasser, G. Martini, U. Manfredi, T. Streibel, M. Sklorz, R. Zimmermann, P. F. DeCarlo, C. Astorga, U. Baltensperger, and A. S. H. Prevot
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acpd-14-16591-2014, https://doi.org/10.5194/acpd-14-16591-2014, 2014
Revised manuscript has not been submitted
M. Crippa, F. Canonaco, V. A. Lanz, M. Äijälä, J. D. Allan, S. Carbone, G. Capes, D. Ceburnis, M. Dall'Osto, D. A. Day, P. F. DeCarlo, M. Ehn, A. Eriksson, E. Freney, L. Hildebrandt Ruiz, R. Hillamo, J. L. Jimenez, H. Junninen, A. Kiendler-Scharr, A.-M. Kortelainen, M. Kulmala, A. Laaksonen, A. A. Mensah, C. Mohr, E. Nemitz, C. O'Dowd, J. Ovadnevaite, S. N. Pandis, T. Petäjä, L. Poulain, S. Saarikoski, K. Sellegri, E. Swietlicki, P. Tiitta, D. R. Worsnop, U. Baltensperger, and A. S. H. Prévôt
Atmos. Chem. Phys., 14, 6159–6176, https://doi.org/10.5194/acp-14-6159-2014, https://doi.org/10.5194/acp-14-6159-2014, 2014
J. W. Halfacre, T. N. Knepp, P. B. Shepson, C. R. Thompson, K. A. Pratt, B. Li, P. K. Peterson, S. J. Walsh, W. R. Simpson, P. A. Matrai, J. W. Bottenheim, S. Netcheva, D. K. Perovich, and A. Richter
Atmos. Chem. Phys., 14, 4875–4894, https://doi.org/10.5194/acp-14-4875-2014, https://doi.org/10.5194/acp-14-4875-2014, 2014
M. Crippa, F. Canonaco, J. G. Slowik, I. El Haddad, P. F. DeCarlo, C. Mohr, M. F. Heringa, R. Chirico, N. Marchand, B. Temime-Roussel, E. Abidi, L. Poulain, A. Wiedensohler, U. Baltensperger, and A. S. H. Prévôt
Atmos. Chem. Phys., 13, 8411–8426, https://doi.org/10.5194/acp-13-8411-2013, https://doi.org/10.5194/acp-13-8411-2013, 2013
M. Laborde, M. Crippa, T. Tritscher, Z. Jurányi, P. F. Decarlo, B. Temime-Roussel, N. Marchand, S. Eckhardt, A. Stohl, U. Baltensperger, A. S. H. Prévôt, E. Weingartner, and M. Gysel
Atmos. Chem. Phys., 13, 5831–5856, https://doi.org/10.5194/acp-13-5831-2013, https://doi.org/10.5194/acp-13-5831-2013, 2013
M. Crippa, P. F. DeCarlo, J. G. Slowik, C. Mohr, M. F. Heringa, R. Chirico, L. Poulain, F. Freutel, J. Sciare, J. Cozic, C. F. Di Marco, M. Elsasser, J. B. Nicolas, N. Marchand, E. Abidi, A. Wiedensohler, F. Drewnick, J. Schneider, S. Borrmann, E. Nemitz, R. Zimmermann, J.-L. Jaffrezo, A. S. H. Prévôt, and U. Baltensperger
Atmos. Chem. Phys., 13, 961–981, https://doi.org/10.5194/acp-13-961-2013, https://doi.org/10.5194/acp-13-961-2013, 2013
Related subject area
Subject: Aerosols | Research Activity: Field Measurements | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Diverse sources and aging change the mixing state and ice nucleation properties of aerosol particles over the western Pacific and Southern Ocean
The water-insoluble organic carbon in PM2.5 of typical Chinese urban areas: light-absorbing properties, potential sources, radiative forcing effects, and a possible light-absorbing continuum
Measurement report: Size-resolved secondary organic aerosol formation modulated by aerosol water uptake in wintertime haze
In situ measurement of organic aerosol molecular markers in urban Hong Kong during a summer period: temporal variations and source apportionment
Technical note: Determining chemical composition of atmospheric single particles by a standard-free mass calibration algorithm
Different formation pathways of nitrogen-containing organic compounds in aerosols and fog water in northern China
Impact of weather patterns and meteorological factors on PM2.5 and O3 responses to the COVID-19 lockdown in China
Daytime and nighttime aerosol soluble iron formation in clean and slightly polluted moist air in a coastal city in eastern China
Non-negligible secondary contribution to brown carbon in autumn and winter: inspiration from particulate nitrated and oxygenated aromatic compounds in urban Beijing
Simultaneous organic aerosol source apportionment at two Antarctic sites reveals large-scale and ecoregion-specific components
Measurement report: Optical characterization, seasonality, and sources of brown carbon in fine aerosols from Tianjin, North China: year-round observations
Bayesian inference-based estimation of hourly primary and secondary organic carbon in suburban Hong Kong: multi-temporal-scale variations and evolution characteristics during PM2.5 episodes
Vertical variability of aerosol properties and trace gases over a remote marine region: A case study over Bermuda
Measurement report: Characteristics of nitrogen-containing organics in PM2.5 in Ürümqi, northwestern China – differential impacts of combustion of fresh and aged biomass materials
Measurement report: Formation of tropospheric brown carbon in a lifting air mass
Measurement report: Bio-physicochemistry of tropical clouds at Maïdo (Réunion, Indian Ocean): overview of results from the BIO-MAÏDO campaign
Chemical properties and single-particle mixing state of soot aerosol in Houston during the TRACER campaign
High Altitude Aerosol Chemical Characterization and Source Identification: Insights from the CALISHTO Campaign
Characterizing water solubility of fresh and aged secondary organic aerosol in PM2.5 with the stable carbon isotope technique
Measurement report: Evaluation of the TOF-ACSM-CV for PM1.0 and PM2.5 measurements during the RITA-2021 field campaign
Sea salt reactivity over the northwest Atlantic: an in-depth look using the airborne ACTIVATE dataset
Measurement report: Atmospheric ice nuclei in the Changbai Mountains (2623 m a.s.l.) in northeastern Asia
Morphological and optical properties of carbonaceous aerosol particles from ship emissions and biomass burning during a summer cruise measurement in the South China Sea
Critical contribution of chemically diverse carbonyl molecules to the oxidative potential of atmospheric aerosols
Tropical tropospheric aerosol sources and chemical composition observed at high altitude in the Bolivian Andes
Chemical composition, sources and formation mechanism of urban PM2.5 in Southwest China: a case study at the beginning of 2023
Chemical characterization of atmospheric aerosols at a high-altitude mountain site: a study of source apportionment
Composition and sources of carbonaceous aerosol in the European Arctic at Zeppelin Observatory, Svalbard (2017 to 2020)
Variation in chemical composition and volatility of oxygenated organic aerosol in different rural, urban, and mountain environments
Elucidating the mechanisms of atmospheric new particle formation in the highly polluted Po Valley, Italy
Differences in aerosol and cloud properties along the central California coast when winds change from northerly to southerly
Diverging trends in aerosol sulfate and nitrate measured in the remote North Atlantic on Barbados are attributed to clean air policies, African smoke, and anthropogenic emissions
Local ship speed reduction effect on black carbon emissions measured at remote marine station
Roles of marine biota in the formation of atmospheric bioaerosols, cloud condensation nuclei, and ice-nucleating particles over the North Pacific Ocean, Bering Sea, and Arctic Ocean
Evolution of nucleophilic high molecular-weight organic compounds in ambient aerosols: a case study
Fractional solubility of iron in mineral dust aerosols over coastal Namibia: a link to marine biogenic emissions?
Real-world observations of reduced nitrogen and ultrafine particles in commercial cooking organic aerosol emissions
Source apportionment of PM2.5 in Montréal, Canada, and health risk assessment for potentially toxic elements
Physicochemical and temporal characteristics of individual atmospheric aerosol particles in urban Seoul during KORUS-AQ campaign: insights from single-particle analysis
Mass spectrometric analysis of unprecedented high levels of carbonaceous aerosol particles long-range transported from wildfires in the Siberian Arctic
Short-term source apportionment of fine particulate matter with time-dependent profiles using SoFi Pro: exploring the reliability of rolling positive matrix factorization (PMF) applied to bihourly molecular and elemental tracer data
Particulate-bound alkyl nitrate pollution and formation mechanisms in Beijing, China
Measurement report: Impact of emission control measures on environmental persistent free radicals and reactive oxygen species – A short-term case study in Beijing
Characterization of water-soluble brown carbon chromophores from wildfire plumes in the western USA using size-exclusion chromatography
Marine carbohydrates in Arctic aerosol particles and fog – diversity of oceanic sources and atmospheric transformations
Investigating the contribution of grown new particles to cloud condensation nuclei with largely varying preexisting particles – Part 1: Observational data analysis
Measurement report: Brown carbon aerosol in polluted urban air of the North China Plain – day–night differences in the chromophores and optical properties
Measurement report: Secondary organic aerosols at a forested mountain site in southeastern China
Source apportionment of soot particles and aqueous-phase processing of black carbon coatings in an urban environment
Measurement report: Characteristics of airborne black carbon-containing particles during the 2021 summer COVID-19 lockdown in Yangzhou, China
Jiao Xue, Tian Zhang, Keyhong Park, Jinpei Yan, Young Jun Yoon, Jiyeon Park, and Bingbing Wang
Atmos. Chem. Phys., 24, 7731–7754, https://doi.org/10.5194/acp-24-7731-2024, https://doi.org/10.5194/acp-24-7731-2024, 2024
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Ice formation by particles is an important way of making mixed-phase and ice clouds. We found that particles collected in the marine atmosphere exhibit diverse ice nucleation abilities and mixing states. Sea salt mixed-sulfate particles were enriched in ice-nucleating particles. Selective aging on sea salt particles made particle populations more externally mixed. Characterizations of particles and their mixing state are needed for a better understanding of aerosol–cloud interactions.
Yangzhi Mo, Jun Li, Guangcai Zhong, Sanyuan Zhu, Shizhen Zhao, Jiao Tang, Hongxing Jiang, Zhineng Cheng, Chongguo Tian, Yingjun Chen, and Gan Zhang
Atmos. Chem. Phys., 24, 7755–7772, https://doi.org/10.5194/acp-24-7755-2024, https://doi.org/10.5194/acp-24-7755-2024, 2024
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In this study, we found that biomass burning (31.0 %) and coal combustion (31.1 %) were the dominant sources of water-insoluble organic carbon in China, with coal combustion sources exhibiting the strongest light-absorbing capacity. Additionally, we propose a light-absorbing carbonaceous continuum, revealing that components enriched with fossil sources tend to have stronger light-absorbing capacity, higher aromaticity, higher molecular weights, and greater recalcitrance in the atmosphere.
Jing Duan, Ru-Jin Huang, Ying Wang, Wei Xu, Haobin Zhong, Chunshui Lin, Wei Huang, Yifang Gu, Jurgita Ovadnevaite, Darius Ceburnis, and Colin O'Dowd
Atmos. Chem. Phys., 24, 7687–7698, https://doi.org/10.5194/acp-24-7687-2024, https://doi.org/10.5194/acp-24-7687-2024, 2024
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The chemical composition of atmospheric particles has shown significant changes in recent years. We investigated the potential effects of changes in inorganics on aerosol water uptake and, thus, secondary organic aerosol formation in wintertime haze based on the size-resolved measurements of non-refractory fine particulate matter (NR-PM2.5) in Xi’an, northwestern China. We highlight the key role of aerosol water as a medium to link inorganics and organics in their multiphase processes.
Hongyong Li, Xiaopu Lyu, Likun Xue, Yunxi Huo, Dawen Yao, Haoxian Lu, and Hai Guo
Atmos. Chem. Phys., 24, 7085–7100, https://doi.org/10.5194/acp-24-7085-2024, https://doi.org/10.5194/acp-24-7085-2024, 2024
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Organic aerosol is ubiquitous in the atmosphere and largely explains the gap between current levels of fine particulate matter in many cities and the World Health Organization guideline values. This study highlights the dominant contributions of cooking emissions to organic aerosol when marine air prevailed in Hong Kong, which were occasionally overwhelmed by aromatics-derived secondary organic aerosol in continental ouflows.
Shao Shi, Jinghao Zhai, Xin Yang, Yechun Ruan, Yuanlong Huang, Xujian Chen, Antai Zhang, Jianhuai Ye, Guomao Zheng, Baohua Cai, Yaling Zeng, Yixiang Wang, Chunbo Xing, Yujie Zhang, Tzung-May Fu, Lei Zhu, Huizhong Shen, and Chen Wang
Atmos. Chem. Phys., 24, 7001–7012, https://doi.org/10.5194/acp-24-7001-2024, https://doi.org/10.5194/acp-24-7001-2024, 2024
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The determination of ions in the mass spectra of individual particles remains uncertain. We have developed a standard-free mass calibration algorithm applicable to more than 98 % of ambient particles. With our algorithm, ions with ~ 0.05 Th mass difference could be determined. Therefore, many more atmospheric species could be determined and involved in the source apportionment of aerosols, the study of chemical reaction mechanisms, and the analysis of single-particle mixing states.
Wei Sun, Xiaodong Hu, Yuzhen Fu, Guohua Zhang, Yujiao Zhu, Xinfeng Wang, Caiqing Yan, Likun Xue, He Meng, Bin Jiang, Yuhong Liao, Xinming Wang, Ping'an Peng, and Xinhui Bi
Atmos. Chem. Phys., 24, 6987–6999, https://doi.org/10.5194/acp-24-6987-2024, https://doi.org/10.5194/acp-24-6987-2024, 2024
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The formation pathways of nitrogen-containing compounds (NOCs) in the atmosphere remain unclear. We investigated the composition of aerosols and fog water by state-of-the-art mass spectrometry and compared the formation pathways of NOCs. We found that NOCs in aerosols were mainly formed through nitration reaction, while ammonia addition played a more important role in fog water. The results deepen our understanding of the processes of organic particulate pollution.
Fuzhen Shen, Michaela I. Hegglin, and Yue Yuan
Atmos. Chem. Phys., 24, 6539–6553, https://doi.org/10.5194/acp-24-6539-2024, https://doi.org/10.5194/acp-24-6539-2024, 2024
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We attempt to use a novel structural self-organising map and machine learning models to identify a weather system and quantify the importance of each meteorological factor in driving the unexpected PM2.5 and O3 changes under the specific weather system during the COVID-19 lockdown in China. The result highlights that temperature under the double-centre high-pressure system plays the most crucial role in abnormal events.
Wenshuai Li, Yuxuan Qi, Yingchen Liu, Guanru Wu, Yanjing Zhang, Jinhui Shi, Wenjun Qu, Lifang Sheng, Wencai Wang, Daizhou Zhang, and Yang Zhou
Atmos. Chem. Phys., 24, 6495–6508, https://doi.org/10.5194/acp-24-6495-2024, https://doi.org/10.5194/acp-24-6495-2024, 2024
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Aerosol particles from mainland can transport to oceans and deposit, providing soluble Fe and affecting phytoplankton growth. Thus, we studied the dissolution process of aerosol Fe and found that photochemistry played a key role in promoting Fe dissolution in clean conditions. RH-dependent reactions were more influential in slightly polluted conditions. These results highlight the distinct roles of two weather-related parameters (radiation and RH) in influencing geochemical cycles related to Fe.
Yanqin Ren, Zhenhai Wu, Yuanyuan Ji, Fang Bi, Junling Li, Haijie Zhang, Hao Zhang, Hong Li, and Gehui Wang
Atmos. Chem. Phys., 24, 6525–6538, https://doi.org/10.5194/acp-24-6525-2024, https://doi.org/10.5194/acp-24-6525-2024, 2024
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Nitrated aromatic compounds (NACs) and oxygenated derivatives of polycyclic aromatic hydrocarbons (OPAHs) in PM2.5 were examined from an urban area in Beijing during the autumn and winter. The OPAH and NAC concentrations were much higher during heating than before heating. They majorly originated from the combustion of biomass and automobile emissions, and the secondary generation was the major contributor throughout the whole sampling period.
Marco Paglione, David C. S. Beddows, Anna Jones, Thomas Lachlan-Cope, Matteo Rinaldi, Stefano Decesari, Francesco Manarini, Mara Russo, Karam Mansour, Roy M. Harrison, Andrea Mazzanti, Emilio Tagliavini, and Manuel Dall'Osto
Atmos. Chem. Phys., 24, 6305–6322, https://doi.org/10.5194/acp-24-6305-2024, https://doi.org/10.5194/acp-24-6305-2024, 2024
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Applying factor analysis techniques to H-NMR spectra, we present the organic aerosol (OA) source apportionment of PM1 samples collected in parallel at two Antarctic stations, namely Signy and Halley, allowing investigation of aerosol–climate interactions in an unperturbed atmosphere. Our results show remarkable differences between pelagic (open-ocean) and sympagic (sea-ice-influenced) air masses and indicate that various sources and processes are controlling Antarctic aerosols.
Zhichao Dong, Chandra Mouli Pavuluri, Peisen Li, Zhanjie Xu, Junjun Deng, Xueyan Zhao, Xiaomai Zhao, Pingqing Fu, and Cong-Qiang Liu
Atmos. Chem. Phys., 24, 5887–5905, https://doi.org/10.5194/acp-24-5887-2024, https://doi.org/10.5194/acp-24-5887-2024, 2024
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Comprehensive study of optical properties of brown carbon (BrC) in fine aerosols from Tianjin, China, implied that biological emissions are major sources of BrC in summer, whereas fossil fuel combustion and biomass burning emissions are in cold periods. The direct radiation absorption caused by BrC in short wavelengths contributed about 40 % to that caused by BrC in 300–700 nm. Water-insoluble but methanol-soluble BrC contains more protein-like chromophores (PLOM) than that of water-soluble BrC.
Shan Wang, Kezheng Liao, Zijing Zhang, Yuk Ying Cheng, Qiongqiong Wang, Hanzhe Chen, and Jian Zhen Yu
Atmos. Chem. Phys., 24, 5803–5821, https://doi.org/10.5194/acp-24-5803-2024, https://doi.org/10.5194/acp-24-5803-2024, 2024
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In this work, hourly primary and secondary organic carbon were estimated by a novel Bayesian inference approach in suburban Hong Kong. Their multi-temporal-scale variations and evolution characteristics during PM2.5 episodes were examined. The methodology could serve as a guide for other locations with similar monitoring capabilities. The observation-based results are helpful for understanding the evolving nature of secondary organic aerosols and refining the accuracy of model simulations.
Taiwo Adedayo Ajayi, Yonghoon Choi, Ewan C. Crosbie, Joshua P. DiGangi, Glenn S. Diskin, Marta A. Fenn, Richard A. Ferrare, Johnathan W. Hair, Miguel Ricardo A. Hilario, Chris A. Hostetler, Simon Kirschler, Richard H. Moore, Taylor J. Shingler, Michael A. Shook, Cassidy Soloff, Kenneth L. Thornhill, Christiane Voigt, Edward L. Winstead, Luke Ziemba, and Armin Sorooshian
EGUsphere, https://doi.org/10.5194/egusphere-2024-1065, https://doi.org/10.5194/egusphere-2024-1065, 2024
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This study uses airborne data to examine vertical profiles of trace gases, aerosol particles, and meteorological variables over a remote marine area (Bermuda). Results show distinct differences based on both air mass source region (North America, Ocean, Caribbean/North Africa) and altitude for a given air mass type. This work highlights the sensitivity of remote marine areas to long-range transport and the importance of considering vertical dependence of trace gas and aerosol properties.
Yi-Jia Ma, Yu Xu, Ting Yang, Hong-Wei Xiao, and Hua-Yun Xiao
Atmos. Chem. Phys., 24, 4331–4346, https://doi.org/10.5194/acp-24-4331-2024, https://doi.org/10.5194/acp-24-4331-2024, 2024
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This study provides field-based evidence about the differential impacts of combustion of fresh and aged biomass materials on aerosol nitrogen-containing organic compounds (NOCs) in different seasons in Ürümqi, bridging the linkages between the observations and previous laboratory studies showing the formation mechanisms of NOCs.
Can Wu, Xiaodi Liu, Ke Zhang, Si Zhang, Cong Cao, Jianjun Li, Rui Li, Fan Zhang, and Gehui Wang
EGUsphere, https://doi.org/10.5194/egusphere-2024-891, https://doi.org/10.5194/egusphere-2024-891, 2024
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Brown carbon (BrC) is prevalent in the troposphere, and can efficiently absorb solar and terrestrial radiation. Our observations manifested that the enhanced light-absorption of BrC relative to black carbon at the tropopause can be attributed to the formation of nitrogen-containing organic compounds through the aqueous-phase reactions of carbonyls with ammonium.
Maud Leriche, Pierre Tulet, Laurent Deguillaume, Frédéric Burnet, Aurélie Colomb, Agnès Borbon, Corinne Jambert, Valentin Duflot, Stéphan Houdier, Jean-Luc Jaffrezo, Mickaël Vaïtilingom, Pamela Dominutti, Manon Rocco, Camille Mouchel-Vallon, Samira El Gdachi, Maxence Brissy, Maroua Fathalli, Nicolas Maury, Bert Verreyken, Crist Amelynck, Niels Schoon, Valérie Gros, Jean-Marc Pichon, Mickael Ribeiro, Eric Pique, Emmanuel Leclerc, Thierry Bourrianne, Axel Roy, Eric Moulin, Joël Barrie, Jean-Marc Metzger, Guillaume Péris, Christian Guadagno, Chatrapatty Bhugwant, Jean-Mathieu Tibere, Arnaud Tournigand, Evelyn Freney, Karine Sellegri, Anne-Marie Delort, Pierre Amato, Muriel Joly, Jean-Luc Baray, Pascal Renard, Angelica Bianco, Anne Réchou, and Guillaume Payen
Atmos. Chem. Phys., 24, 4129–4155, https://doi.org/10.5194/acp-24-4129-2024, https://doi.org/10.5194/acp-24-4129-2024, 2024
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Aerosol particles in the atmosphere play a key role in climate change and air pollution. A large number of aerosol particles are formed from the oxidation of volatile organic compounds (VOCs and secondary organic aerosols – SOA). An important field campaign was organized on Réunion in March–April 2019 to understand the formation of SOA in a tropical atmosphere mostly influenced by VOCs emitted by forest and in the presence of clouds. This work synthesizes the results of this campaign.
Ryan N. Farley, James E. Lee, Laura-Hélèna Rivellini, Alex K. Y. Lee, Rachael Dal Porto, Christopher D. Cappa, Kyle Gorkowski, Abu Sayeed Md Shawon, Katherine B. Benedict, Allison C. Aiken, Manvendra K. Dubey, and Qi Zhang
Atmos. Chem. Phys., 24, 3953–3971, https://doi.org/10.5194/acp-24-3953-2024, https://doi.org/10.5194/acp-24-3953-2024, 2024
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The black carbon aerosol composition and mixing state were characterized using a soot particle aerosol mass spectrometer. Single-particle measurements revealed the major role of atmospheric processing in modulating the black carbon mixing state. A significant fraction of soot particles were internally mixed with oxidized organic aerosol and sulfate, with implications for activation as cloud nuclei.
Olga Zografou, Maria Gini, Prodromos Fetfatzis, Konstantinos Granakis, Romanos Foskinis, Manousos Ioannis Manousakas, Fotios Tsopelas, Evangelia Diapouli, Eleni Dovrou, Christina N. Vasilakopoulou, Alexandros Papayannis, Spyros N. Pandis, Athanasios Nenes, and Konstantinos Eleftheriadis
EGUsphere, https://doi.org/10.5194/egusphere-2024-737, https://doi.org/10.5194/egusphere-2024-737, 2024
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PM1 chemical characterization and PMF source apportionment on the combined organic and inorganic fraction took place at the high-altitude (HAC)2 station. Cloud presence was found to reduce PM1 concentrations, affecting sulphate more than organics. Interstitial aerosol was richer in low hygroscopic organics and acidic inorganics, compared to activated. Higher relative abundance of eBC compared to the other components was revealed for FT conditions compared to PBL.
Fenghua Wei, Xing Peng, Liming Cao, Mengxue Tang, Ning Feng, Xiaofeng Huang, and Lingyan He
EGUsphere, https://doi.org/10.5194/egusphere-2024-736, https://doi.org/10.5194/egusphere-2024-736, 2024
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The water solubility of secondary organic aerosols (SOA) is a crucial factor in determining their hygroscopicity and climatic impact. Stable carbon isotope and mass spectrometry techniques were combined to assess the water solubility of SOA with different aging degrees in a coastal megacity in China. This work revealed a much higher water-soluble fraction of aged SOA compared to fresh SOA, indicating that the aging degree of SOA has considerable impacts on its water solubility.
Xinya Liu, Bas Henzing, Arjan Hensen, Jan Mulder, Peng Yao, Danielle van Dinther, Jerry van Bronckhorst, Rujin Huang, and Ulrike Dusek
Atmos. Chem. Phys., 24, 3405–3420, https://doi.org/10.5194/acp-24-3405-2024, https://doi.org/10.5194/acp-24-3405-2024, 2024
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We evaluated the time-of-flight aerosol chemical speciation monitor (TOF-ACSM) following the implementation of the PM2.5 aerodynamic lens and a capture vaporizer (CV). The results showed that it significantly improved the accuracy and precision of ACSM in the field observations. The paper elucidates the measurement outcomes of various instruments and provides an analysis of their biases. This comprehensive evaluation is expected to benefit the ACSM community and other aerosol field measurements.
Eva-Lou Edwards, Yonghoon Choi, Ewan C. Crosbie, Joshua P. DiGangi, Glenn S. Diskin, Claire E. Robinson, Michael A. Shook, Edward L. Winstead, Luke D. Ziemba, and Armin Sorooshian
Atmos. Chem. Phys., 24, 3349–3378, https://doi.org/10.5194/acp-24-3349-2024, https://doi.org/10.5194/acp-24-3349-2024, 2024
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We investigate Cl− depletion in sea salt particles over the northwest Atlantic from December 2021 to June 2022 using an airborne dataset. Losses of Cl− are greatest in May and least in December–February and March. Inorganic acidic species can account for all depletion observed for December–February, March, and June near Bermuda but none in May. Quantifying Cl− depletion as a percentage captures seasonal trends in depletion but fails to convey the effects it may have on atmospheric oxidation.
Yue Sun, Yujiao Zhu, Yanbin Qi, Lanxiadi Chen, Jiangshan Mu, Ye Shan, Yu Yang, Yanqiu Nie, Ping Liu, Can Cui, Ji Zhang, Mingxuan Liu, Lingli Zhang, Yufei Wang, Xinfeng Wang, Mingjin Tang, Wenxing Wang, and Likun Xue
Atmos. Chem. Phys., 24, 3241–3256, https://doi.org/10.5194/acp-24-3241-2024, https://doi.org/10.5194/acp-24-3241-2024, 2024
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Field observations were conducted at the summit of Changbai Mountain in northeast Asia. The cumulative number concentration of ice-nucleating particles (INPs) varied from 1.6 × 10−3 to 78.3 L−1 over the temperature range of −5.5 to −29.0 ℃. Biological INPs (bio-INPs) accounted for the majority of INPs, and the proportion exceeded 90% above −13.0 ℃. Planetary boundary layer height, valley breezes, and long-distance transport of air mass influence the abundance of bio-INPs.
Cuizhi Sun, Yongyun Zhang, Baoling Liang, Min Gao, Xi Sun, Fei Li, Xue Ni, Qibin Sun, Hengjia Ou, Dexian Chen, Shengzhen Zhou, and Jun Zhao
Atmos. Chem. Phys., 24, 3043–3063, https://doi.org/10.5194/acp-24-3043-2024, https://doi.org/10.5194/acp-24-3043-2024, 2024
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In a May–June 2021 expedition in the South China Sea, we analyzed black and brown carbon in marine aerosols, key to light absorption and climate impact. Using advanced in situ and microscope techniques, we observed particle size, structure, and tar balls mixed with various elements. Results showed biomass burning and fossil fuels majorly influence light absorption, especially during significant burning events. This research aids the understanding of carbonaceous aerosols' role in marine climate.
Feifei Li, Shanshan Tang, Jitao Lv, Shiyang Yu, Xu Sun, Dong Cao, Yawei Wang, and Guibin Jiang
EGUsphere, https://doi.org/10.5194/egusphere-2024-37, https://doi.org/10.5194/egusphere-2024-37, 2024
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Targeted derivatization and non-targeted analysis with FT-ICR MS were used to reveal the molecular composition of carbonyl molecules in PM2.5, and the important role of carbonyls in increasing the oxidative potential of organic aerosol was found in the real samples.
C. Isabel Moreno, Radovan Krejci, Jean-Luc Jaffrezo, Gaëlle Uzu, Andrés Alastuey, Marcos F. Andrade, Valeria Mardóñez, Alkuin Maximilian Koenig, Diego Aliaga, Claudia Mohr, Laura Ticona, Fernando Velarde, Luis Blacutt, Ricardo Forno, David N. Whiteman, Alfred Wiedensohler, Patrick Ginot, and Paolo Laj
Atmos. Chem. Phys., 24, 2837–2860, https://doi.org/10.5194/acp-24-2837-2024, https://doi.org/10.5194/acp-24-2837-2024, 2024
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Aerosol chemical composition (ions, sugars, carbonaceous matter) from 2011 to 2020 was studied at Mt. Chacaltaya (5380 m a.s.l., Bolivian Andes). Minimum concentrations occur in the rainy season with maxima in the dry and transition seasons. The origins of the aerosol are located in a radius of hundreds of kilometers: nearby urban and rural areas, natural biogenic emissions, vegetation burning from Amazonia and Chaco, Pacific Ocean emissions, soil dust, and Peruvian volcanism.
Junke Zhang, Yunfei Su, Chunying Chen, Wenkai Guo, Qinwen Tan, Miao Feng, Danlin Song, Tao Jiang, Qiang Chen, Yuan Li, Wei Li, Yizhi Wang, Xiaojuan Huang, Lin Han, Wanqing Wu, and Gehui Wang
Atmos. Chem. Phys., 24, 2803–2820, https://doi.org/10.5194/acp-24-2803-2024, https://doi.org/10.5194/acp-24-2803-2024, 2024
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Typical haze events in Chengdu at the beginning of 2023 were investigated with bulk-chemical and single-particle analyses along with numerical model simulations. By integrating the obtained chemical composition, source, mixing state and numerical simulation results, we infer that Haze-1 was mainly caused by pollutants related to fossil fuel combustion, especially local mobile sources, while Haze-2 was triggered by the secondary pollutants, which mainly came from regional transmission.
Elena Barbaro, Matteo Feltracco, Fabrizio De Blasi, Clara Turetta, Marta Radaelli, Warren Cairns, Giulio Cozzi, Giovanna Mazzi, Marco Casula, Jacopo Gabrieli, Carlo Barbante, and Andrea Gambaro
Atmos. Chem. Phys., 24, 2821–2835, https://doi.org/10.5194/acp-24-2821-2024, https://doi.org/10.5194/acp-24-2821-2024, 2024
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The study analyzed a year of atmospheric aerosol composition at Col Margherita in the Italian Alps. Over 100 chemical markers were identified, including major ions, organic compounds, and trace elements. It revealed sources of aerosol, highlighted impacts of Saharan dust events, and showed anthropogenic pollution's influence despite the site's remoteness. Enrichment factors emphasized non-natural sources of trace elements. Source apportionment identified four key factors affecting the area.
Karl Espen Yttri, Are Bäcklund, Franz Conen, Sabine Eckhardt, Nikolaos Evangeliou, Markus Fiebig, Anne Kasper-Giebl, Avram Gold, Hans Gundersen, Cathrine Lund Myhre, Stephen Matthew Platt, David Simpson, Jason D. Surratt, Sönke Szidat, Martin Rauber, Kjetil Tørseth, Martin Album Ytre-Eide, Zhenfa Zhang, and Wenche Aas
Atmos. Chem. Phys., 24, 2731–2758, https://doi.org/10.5194/acp-24-2731-2024, https://doi.org/10.5194/acp-24-2731-2024, 2024
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We discuss carbonaceous aerosol (CA) observed at the high Arctic Zeppelin Observatory (2017 to 2020). We find that organic aerosol is a significant fraction of the Arctic aerosol, though less than sea salt aerosol and mineral dust, as well as non-sea-salt sulfate, originating mainly from anthropogenic sources in winter and from natural sources in summer, emphasizing the importance of wildfires for biogenic secondary organic aerosol and primary biological aerosol particles observed in the Arctic.
Wei Huang, Cheng Wu, Linyu Gao, Yvette Gramlich, Sophie L. Haslett, Joel Thornton, Felipe D. Lopez-Hilfiker, Ben H. Lee, Junwei Song, Harald Saathoff, Xiaoli Shen, Ramakrishna Ramisetty, Sachchida N. Tripathi, Dilip Ganguly, Feng Jiang, Magdalena Vallon, Siegfried Schobesberger, Taina Yli-Juuti, and Claudia Mohr
Atmos. Chem. Phys., 24, 2607–2624, https://doi.org/10.5194/acp-24-2607-2024, https://doi.org/10.5194/acp-24-2607-2024, 2024
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We present distinct molecular composition and volatility of oxygenated organic aerosol particles in different rural, urban, and mountain environments. We do a comprehensive investigation of the relationship between the chemical composition and volatility of oxygenated organic aerosol particles across different systems and environments. This study provides implications for volatility descriptions of oxygenated organic aerosol particles in different model frameworks.
Jing Cai, Juha Sulo, Yifang Gu, Sebastian Holm, Runlong Cai, Steven Thomas, Almuth Neuberger, Fredrik Mattsson, Marco Paglione, Stefano Decesari, Matteo Rinaldi, Rujing Yin, Diego Aliaga, Wei Huang, Yuanyuan Li, Yvette Gramlich, Giancarlo Ciarelli, Lauriane Quéléver, Nina Sarnela, Katrianne Lehtipalo, Nora Zannoni, Cheng Wu, Wei Nie, Juha Kangasluoma, Claudia Mohr, Markku Kulmala, Qiaozhi Zha, Dominik Stolzenburg, and Federico Bianchi
Atmos. Chem. Phys., 24, 2423–2441, https://doi.org/10.5194/acp-24-2423-2024, https://doi.org/10.5194/acp-24-2423-2024, 2024
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By combining field measurements, simulations and recent chamber experiments, we investigate new particle formation (NPF) and growth in the Po Valley, where both haze and frequent NPF occur. Our results show that sulfuric acid, ammonia and amines are the dominant NPF precursors there. A high NPF rate and a lower condensation sink lead to a greater survival probability for newly formed particles, highlighting the importance of gas-to-particle conversion for aerosol concentrations.
Kira Zeider, Grace Betito, Anthony Bucholtz, Peng Xian, Annette Walker, and Armin Sorooshian
EGUsphere, https://doi.org/10.5194/egusphere-2024-392, https://doi.org/10.5194/egusphere-2024-392, 2024
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The predominant wind direction along the California coast (northerly) reverses several times during the summer (to southerly). The effects of these wind reversals on aerosol and cloud characteristics are not well understood. Using data from multiple datasets we found that southerly flow periods had enhanced signatures of anthropogenic emissions due to shipping/continental sources, and clouds had more but smaller droplets.
Cassandra J. Gaston, Joseph M. Prospero, Kristen Foley, Havala O. T. Pye, Lillian Custals, Edmund Blades, Peter Sealy, and James A. Christie
EGUsphere, https://doi.org/10.5194/egusphere-2024-11, https://doi.org/10.5194/egusphere-2024-11, 2024
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To understand how changing emissions have impacted aerosols in remote regions, we measured nitrate and sulfate at Barbados and compared to model predictions from EPA’s Air QUAlity TimE Series (EQUATES). Nitrate was stable except for spikes in 2008 and 2010 due to transported smoke. Sulfate decreased in the 1990s due to reductions of sulfur dioxide (SO2) in the U.S. and Europe, then increased in the 2000s due to anthropogenic emissions from Africa and more efficient oxidation of SO2.
Mikko Heikkilä, Krista Luoma, Timo Mäkelä, and Tiia Grönholm
EGUsphere, https://doi.org/10.5194/egusphere-2023-2823, https://doi.org/10.5194/egusphere-2023-2823, 2024
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Black carbon (BC) concentration was measured from 211 ship exhaust gas plumes at a remote marine station. Emission factors of BC were calculated in grams/kilograms fuel. Ships using exhaust gas cleaning systems (EGCS) were found to emit 80 % less BC than ships without EGCS. Emission factors were used to model BC emissions as a function of speed to define the effect of speed reduction. BC emissions increased with a decrease in speed from the ship’s service speed.
Kaori Kawana, Fumikazu Taketani, Kazuhiko Matsumoto, Yutaka Tobo, Yoko Iwamoto, Takuma Miyakawa, Akinori Ito, and Yugo Kanaya
Atmos. Chem. Phys., 24, 1777–1799, https://doi.org/10.5194/acp-24-1777-2024, https://doi.org/10.5194/acp-24-1777-2024, 2024
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Based on comprehensive shipborne observations, we found strong links between sea-surface biological materials and the formation of atmospheric fluorescent bioaerosols, cloud condensation nuclei, and ice-nucleating particles over the Arctic Ocean and Bering Sea during autumn 2019. Taking the wind-speed effect into account, we propose equations to approximate the links for this cruise, which can be used as a guide for modeling as well as for systematic comparisons with other observations.
Chen He, Hanxiong Che, Zier Bao, Yiliang Liu, Qing Li, Miao Hu, Jiawei Zhou, Shumin Zhang, Xiaojiang Yao, Quan Shi, Chunmao Chen, Yan Han, Lingshuo Meng, Xin Long, Fumo Yang, and Yang Chen
Atmos. Chem. Phys., 24, 1627–1639, https://doi.org/10.5194/acp-24-1627-2024, https://doi.org/10.5194/acp-24-1627-2024, 2024
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We examined the daily evolution of high molecular-weight organic compounds with a molecular weight of up to 1000 Da in order to comprehend their behaviors in the atmosphere under actual conditions. These compounds were proven to undergo multi-generation oxidation, carboxylation, and nitrification via both day- and nighttime chemistry.
Karine Desboeufs, Paola Formenti, Raquel Torres-Sánchez, Kerstin Schepanski, Jean-Pierre Chaboureau, Hendrik Andersen, Jan Cermak, Stefanie Feuerstein, Benoit Laurent, Danitza Klopper, Andreas Namwoonde, Mathieu Cazaunau, Servanne Chevaillier, Anaïs Feron, Cécile Mirande-Bret, Sylvain Triquet, and Stuart J. Piketh
Atmos. Chem. Phys., 24, 1525–1541, https://doi.org/10.5194/acp-24-1525-2024, https://doi.org/10.5194/acp-24-1525-2024, 2024
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This study investigates the fractional solubility of iron (Fe) in dust particles along the coast of Namibia, a critical region for the atmospheric Fe supply of the South Atlantic Ocean. Our results suggest a possible two-way interplay whereby marine biogenic emissions from the coastal marine ecosystems into the atmosphere would increase the solubility of Fe-bearing dust by photo-reduction processes. The subsequent deposition of soluble Fe could act to further enhance marine biogenic emissions.
Sunhye Kim, Jo Machesky, Drew R. Gentner, and Albert A. Presto
Atmos. Chem. Phys., 24, 1281–1298, https://doi.org/10.5194/acp-24-1281-2024, https://doi.org/10.5194/acp-24-1281-2024, 2024
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Cooking emissions are often an overlooked source of air pollution. We used a mobile lab to measure the characteristics of particles emitted from cooking sites in two cities. Our findings showed that cooking releases a substantial number of fine particles. While most emissions were similar, a bakery site showed distinctive chemical compositions with higher nitrogen compound levels. Thus, understanding the particle emissions from different cooking activities is crucial.
Nansi Fakhri, Robin Stevens, Arnold Downey, Konstantina Oikonomou, Jean Sciare, Charbel Afif, and Patrick L. Hayes
Atmos. Chem. Phys., 24, 1193–1212, https://doi.org/10.5194/acp-24-1193-2024, https://doi.org/10.5194/acp-24-1193-2024, 2024
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We investigated the chemical composition of atmospheric fine particles, their emission sources, and the potential human health risk associated with trace elements in particles for an urban site in Montréal over a 3-month period (August–November). This study represents the first time that such extensive composition measurements were included in an urban source apportionment study in Canada, and it provides greater resolution of fine-particle sources than has been previously achieved in Canada.
Hanjin Yoo, Li Wu, Hong Geng, and Chul-Un Ro
Atmos. Chem. Phys., 24, 853–867, https://doi.org/10.5194/acp-24-853-2024, https://doi.org/10.5194/acp-24-853-2024, 2024
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We conducted an investigation of atmospheric aerosols collected in Seoul, South Korea, during the KORUS-AQ campaign on a single-particle basis. We were able to identify their sources, the atmospheric fate, and the impacts of local emissions and long-range transport on aerosol composition. Additionally, we traced potential sources of non-exhaust heavy-metal particles. This comprehensive analysis provides valuable insights into the complex dynamics of urban aerosols.
Eric Schneider, Hendryk Czech, Olga Popovicheva, Marina Chichaeva, Vasily Kobelev, Nikolay Kasimov, Tatiana Minkina, Christopher Paul Rüger, and Ralf Zimmermann
Atmos. Chem. Phys., 24, 553–576, https://doi.org/10.5194/acp-24-553-2024, https://doi.org/10.5194/acp-24-553-2024, 2024
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This study provides insights into the complex chemical composition of long-range-transported wildfire plumes from Yakutia, which underwent different levels of atmospheric processing. With complementary mass spectrometric techniques, we improve our understanding of the chemical processes and atmospheric fate of wildfire plumes. Unprecedented high levels of carbonaceous aerosols crossed the polar circle with implications for the Arctic ecosystem and consequently climate.
Qiongqiong Wang, Shuhui Zhu, Shan Wang, Cheng Huang, Yusen Duan, and Jian Zhen Yu
Atmos. Chem. Phys., 24, 475–486, https://doi.org/10.5194/acp-24-475-2024, https://doi.org/10.5194/acp-24-475-2024, 2024
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We investigated short-term source apportionment of PM2.5 utilizing rolling positive matrix factorization (PMF) and online PM chemical speciation data, which included source-specific organic tracers collected over a period of 37 d during the winter of 2019–2020 in suburban Shanghai, China. The findings highlight that by imposing constraints on the primary source profiles, short-term PMF analysis successfully replicated both the individual primary sources and the total secondary sources.
Jiyuan Yang, Guoyang Lei, Jinfeng Zhu, Yutong Wu, Chang Liu, Kai Hu, Junsong Bao, Zitong Zhang, Weili Lin, and Jun Jin
Atmos. Chem. Phys., 24, 123–136, https://doi.org/10.5194/acp-24-123-2024, https://doi.org/10.5194/acp-24-123-2024, 2024
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The atmospheric pollution and formation mechanisms of particulate-bound alkyl nitrate in Beijing were studied. C9–C16 long-chain n-alkyl nitrates negatively correlated with O3 but positively correlated with PM2.5 and NO2, so they may not be produced during gas-phase homogeneous reactions in the photochemical process but form through reactions between alkanes and nitrates on PM surfaces. Particulate-bound n-alkyl nitrates strongly affect both haze pollution and atmospheric visibility.
Yuanyuan Qin, Xinghua Zhang, Wei Huang, Juanjuan Qin, Xiaoyu Hu, Yuxuan Cao, Tianyi Zhao, Yang Zhang, Jihua Tan, Ziyin Zhang, Xinming Wang, and Zhenzhen Wang
EGUsphere, https://doi.org/10.5194/egusphere-2023-2703, https://doi.org/10.5194/egusphere-2023-2703, 2024
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Environmental persistent free radicals (EPFRs) and reactive oxygen species (ROS) play an active role in the atmosphere. We quantified the impact of control measures on EPFRs and ROS and found that strict control measures have effectively reduced their emissions, largely linked to a significant decrease in secondary aerosols. Our findings have great implications for further understanding the formation and sources and for developing future air quality management policies targeting EPFRs and ROS.
Lisa Azzarello, Rebecca A. Washenfelder, Michael A. Robinson, Alessandro Franchin, Caroline C. Womack, Christopher D. Holmes, Steven S. Brown, Ann Middlebrook, Tim Newberger, Colm Sweeney, and Cora J. Young
Atmos. Chem. Phys., 23, 15643–15654, https://doi.org/10.5194/acp-23-15643-2023, https://doi.org/10.5194/acp-23-15643-2023, 2023
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We present a molecular size-resolved offline analysis of water-soluble brown carbon collected on an aircraft during FIREX-AQ. The smoke plumes were aged 0 to 5 h, where absorption was dominated by small molecular weight molecules, brown carbon absorption downwind did not consistently decrease, and the measurements differed from online absorption measurements of the same samples. We show how differences between online and offline absorption could be related to different measurement conditions.
Sebastian Zeppenfeld, Manuela van Pinxteren, Markus Hartmann, Moritz Zeising, Astrid Bracher, and Hartmut Herrmann
Atmos. Chem. Phys., 23, 15561–15587, https://doi.org/10.5194/acp-23-15561-2023, https://doi.org/10.5194/acp-23-15561-2023, 2023
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Marine carbohydrates are produced in the surface of the ocean, enter the atmophere as part of sea spray aerosol particles, and potentially contribute to the formation of fog and clouds. Here, we present the results of a sea–air transfer study of marine carbohydrates conducted in the high Arctic. Besides a chemo-selective transfer, we observed a quick atmospheric aging of carbohydrates, possibly as a result of both biotic and abiotic processes.
Xing Wei, Yanjie Shen, Xiao-Ying Yu, Yang Gao, Huiwang Gao, Ming Chu, Yujiao Zhu, and Xiaohong Yao
Atmos. Chem. Phys., 23, 15325–15350, https://doi.org/10.5194/acp-23-15325-2023, https://doi.org/10.5194/acp-23-15325-2023, 2023
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We investigate the contribution of grown new particles to Nccn at a rural mountain site in the North China Plain. The total particle number concentrations (Ncn) observed on 8 new particle formation (NPF) days were higher compared to non-NPF days. The Nccn at 0.2 % supersaturation (SS) and 0.4 % SS on the NPF days was significantly lower than on non-NPF days. Only one of eight NPF events had detectable net contributions to Nccn at 0.4 % SS and 1.0 % SS with increased κ values.
Yuquan Gong, Ru-Jin Huang, Lu Yang, Ting Wang, Wei Yuan, Wei Xu, Wenjuan Cao, Yang Wang, and Yongjie Li
Atmos. Chem. Phys., 23, 15197–15207, https://doi.org/10.5194/acp-23-15197-2023, https://doi.org/10.5194/acp-23-15197-2023, 2023
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This study reveals the large day–night differences in brown carbon (BrC) chromophore composition, which was not known previously. The results provide insights into the effects of atmospheric processes and emissions on BrC composition.
Zijun Zhang, Weiqi Xu, Yi Zhang, Wei Zhou, Xiangyu Xu, Aodong Du, Yinzhou Zhang, Hongqin Qiao, Ye Kuang, Xiaole Pan, Zifa Wang, Xueling Cheng, Lanzhong Liu, Qingyang Fu, Douglas R. Worsnop, Jie Li, and Yele Sun
EGUsphere, https://doi.org/10.5194/egusphere-2023-2684, https://doi.org/10.5194/egusphere-2023-2684, 2023
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We investigated aerosol composition, sources, and the interaction between secondary organic aerosol (SOA) and clouds at a regional mountain site in southeastern China. Clouds efficiently scavenge more-oxidized SOA; however, cloud evaporation leads to the production of less-oxidized SOA. The unexpectedly high presence of nitrate in aerosol particles indicates that nitrate formed in polluted areas has undergone interactions with clouds, significantly influencing the regional background site.
Ryan N. Farley, Sonya Collier, Christopher D. Cappa, Leah R. Williams, Timothy B. Onasch, Lynn M. Russell, Hwajin Kim, and Qi Zhang
Atmos. Chem. Phys., 23, 15039–15056, https://doi.org/10.5194/acp-23-15039-2023, https://doi.org/10.5194/acp-23-15039-2023, 2023
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Soot particles, also known as black carbon (BC), have important implications for global climate and regional air quality. After the particles are emitted, BC can be coated with other material, impacting the aerosol properties. We selectively measured the composition of particles containing BC to explore their sources and chemical transformations in the atmosphere. We focus on a persistent, multiday fog event in order to study the effects of chemical reactions occurring within liquid droplets.
Yuan Dai, Junfeng Wang, Houjun Wang, Shijie Cui, Yunjiang Zhang, Haiwei Li, Yun Wu, Ming Wang, Eleonora Aruffo, and Xinlei Ge
EGUsphere, https://doi.org/10.5194/egusphere-2023-2454, https://doi.org/10.5194/egusphere-2023-2454, 2023
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Short-term strict emission control can improve air quality but the effectiveness requires assessment. During 2021 summer COVID-19 lockdown in Yangzhou, we showed that the PM2.5 level did not decrease with decrease of gaseous pollutants as aged black carbon-containing particles increased substantially, due to enhanced atmospheric oxidizing capacity and high relative humidity. The results highlights the importance of a regionally balanced control strategy for future air quality management.
Cited articles
Allan, J. D., Bower, K. N., Coe, H., Boudries, H., Jayne, J. T., Canagaratna,
M. R., Millet, D. B., Goldstein, A. H., Quinn, P. K., Weber, R. J., and
Worsnop, D. R.: Submicron aerosol composition at Trinidad Head, California,
during ITCT 2K2: Its relationship with gas phase volatile organic carbon and
assessment of instrument performance, J. Geophys. Res.-Atmos., 109, D23S24,
https://doi.org/10.1029/2003JD004208, 2004.
Ariya, P. A., Dastroor, A. P., Amyot, M., Schroeder, W. H., Barrie, L., Anlauf,
K., Raofie, F., Ryzhkov, A., Davignon, D., Lalonde, J., and Steffen, A.: The
Arctic: a sink for mercury, Tellus B, 56, 397–403, 2004.
Barrie, L. A., Staebler, R., Toom, D., Georgi, B., den Hartog, G.,
Landsberger, S., and Wu, D.: Arctic aerosol size-segregated chemical
observations in relation to ozone depletion during Polar Sunrise Experiment
1992, J. Geophys. Res.-Atmos., 99, 25439–25451, https://doi.org/10.1029/94JD01514,
1994.
Bartels-Rausch, T., Jacobi, H.-W., Kahan, T. F., Thomas, J. L., Thomson, E.
S., Abbatt, J. P. D., Ammann, M., Blackford, J. R., Bluhm, H., Boxe, C.,
Domine, F., Frey, M. M., Gladich, I., Guzmán, M. I., Heger, D., Huthwelker,
Th., Klán, P., Kuhs, W. F., Kuo, M. H., Maus, S., Moussa, S. G., McNeill,
V. F., Newberg, J. T., Pettersson, J. B. C., Roeselová, M., and Sodeau, J.
R.: A review of air–ice chemical and physical interactions (AICI): liquids,
quasi-liquids, and solids in snow, Atmos. Chem. Phys., 14, 1587–1633,
https://doi.org/10.5194/acp-14-1587-2014, 2014.
Beresheim, H. and Eisele, F. L.: Sulfur chemistry in the Antarctic
troposphere experiment: an overview of project SCATE, J. Geophys. Res., 103,
1619–1627, 1998.
Burd, J. A., Peterson, P. K., Nghiem, S. V., Perovich, D. K., and Simpson, W. R.:
Snowmelt onset hinders bromine monoxide heterogeneous recycling in the
Arctic, J. Geophys. Res., 122, 8297–8309, https://doi.org/10.1002/2017JD026906, 2017.
Buys, Z., Brough, N., Huey, L. G., Tanner, D. J., von Glasow, R., and Jones,
A. E.: High temporal resolution Br2, BrCl and BrO observations in
coastal Antarctica, Atmos. Chem. Phys., 13, 1329–1343,
https://doi.org/10.5194/acp-13-1329-2013, 2013.
Cadle, R. D., Fischer, W. H., Frank, E. R., and Lodge Jr., J. P.: Particles in the
Antarctic atmosphere, J. Atmos. Sci., 25, 100–103, 1968.
Canagaratna, M. R., Jayne, J. T., Jiminez, J. L., Allan, J. D., Alfarra, M. R.,
Zhang, Q., Onasch, T. B., Drewnick, F., Coe, H., Middlebrook, A., Delia, A.,
Williams, L. R., Trimborn, A. M., Northway, M. J., DeCarlo, P. F., Kolb, C.
E., Davidovits, P., and Worsnop, D. R.: Chemical and microphysical
characterization of ambient aerosols with the aerodyne aerosol mass
spectrometer, Mass Spectrom. Rev., 26, 185–222, https://doi.org/10.1002/mas.20115, 2007.
Cochran, R. E., Laskina, O., Jayarathne, T., Laskin, A., Laskin, J., Lin, P.,
Sultana, C., Lee, C., Moore, K. A., Cappa, C. D., Bertram, T. H., Prather, K.
A., Grassian, V. H., and Stone, E. A.: Analysis of organic anionic
surfactants in fine and coarse fractions of freshly emitted sea spray
aerosol, Environ. Sci. Technol., 50, 2477–2486,
https://doi.org/10.1021/acs.est.5b04053, 2016.
Comola, F., Kok, J. F., Haume, J., Paterna, E., and Lehning, M.:
Fragmentation of wind-blown snow crystals, Geophys. Res. Lett., 44,
4195–4203, https://doi.org/10.1002/2017GL073039, 2017.
Custard, K. D., Raso, A. R. W., Shepson, P. B., Staebler, R. M., and Pratt, K. A.:
Production and Release of Molecular Bromine and Chlorine from the Arctic
Coastal Snowpack, ACS Earth and Space Chem., 1, 142–151,
https://doi.org/10.1021/acsearthspacechem.7b00014, 2017.
Comiso, J., Parkinson, C., Markus, T., Cavalieri, D., and Gersten, R.:
Current State of the Sea-Ice Cover. National Aeronautics and Space
Admisitration (NASA), Cryosphere, Science Research Portal, available at:
https://neptune.gsfc.nasa.gov/csb/index.php?section=234, last access: 4
April 2018.
Comola, F., Kok, J.F., Gaume, J., Paterna, E. and Lehning, M.: Fragmentation
of wind-blown snow crystals, Geophys. Res. Lett., 44, 4195–4203, 2017.
DeCarlo, P. F., Kimmel, J. R., Trimborn, A., Northway, M. J., Jayne, J. T.,
Aiken, A. C., Gonin, M., Fuhrer, K., Horvath, T., Docherty, K. S., Worsnop,,
D. R., and Jimenez, J. L.: Field-Deployable, High-Resolution, Time-of-Flight
Aerosol Mass Spectrometer, Anal. Chem., 78, 8281–8289, 2006.
DeCarlo, P., Giordano, M., and Kalnajs, L.: 2ODIAC,
https://doi.org/10.17605/OSF.IO/SBW5J, 2018.
Draxler, R. and Rolph, G.: HYSPLIT (HYbrid Single-Particle Lagrangian
Integrated Trajectory) Model access via NOAA ARL READY Website, available at:
http://ready.arl.noaa.gov/HYSPLIT.php (last access: 1 July 2018), NOAA
Air Resources Laboratory, Silver Spring, MD, 2015.
Drewnick, F., Diesch, J.-M., Faber, P., and Borrmann, S.: Aerosol mass
spectrometry: particle–vaporizer interactions and their consequences for the
measurements, Atmos. Meas. Tech., 8, 3811–3830,
https://doi.org/10.5194/amt-8-3811-2015, 2015.
Duce, R. A., Zoller, W. H., and Moyers, J. L.: Particulate and gaseous
halogens in the Antarctic atmosphere, J. Geophys. Res., 78, 7802–7811, 1973.
Eom, H.-J., Gupta, D., Cho, H.-R., Hwang, H. J., Hur, S. D., Gim, Y., and Ro,
C.-U.: Single-particle investigation of summertime and wintertime Antarctic
sea spray aerosols using low-Z particle EPMA, Raman microspectrometry, and
ATR-FTIR imaging techniques, Atmos. Chem. Phys., 16, 13823–13836,
https://doi.org/10.5194/acp-16-13823-2016, 2016.
Finlayson-Pitts, B. J.: The Tropospheric Chemistry of Sea Salt:? A
Molecular-Level View of the Chemistry of NaCl and NaBr, Chem. Rev., 103,
4801–4822, https://doi.org/10.1021/cr020653t, 2003.
Fischer, W. H., Lodge, J. P., Pate, J. B., and Cadle, R. D.: Antarctic
atmospheric chemistry: Preliminary exploration, Science, 164, 66–67,
1969.
Friedmann, E. I.: Endolithic Microorganisms in the Antarctic Cold Desert,
Science, 215, 1045–1053, https://doi.org/10.1126/science.215.4536.1045, 1982.
Gantt, B., Meskhidze, N., Facchini, M. C., Rinaldi, M., Ceburnis, D., and
O'Dowd, C. D.: Wind speed dependent size-resolved parameterization for the
organic mass fraction of sea spray aerosol, Atmos. Chem. Phys., 11,
8777–8790, https://doi.org/10.5194/acp-11-8777-2011, 2011.
Gladney, E. S., Zoller, W. H., Duce, R. A., and Jones, A. G.: Vanadium,
aluminum, and manganese in atmospheric particulates from McMurdo and South
Pole Stations, Antarct. J. US, VII, 171–173, 1972.
Gras, J. L. and Adriaansen, A.: Concentration and size variation of
condensation nuclei at Mawson, Antarctica, J. Atmos. Chem., 3, 93–106, 1985.
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.
Halfacre, J. W., Knepp, T. N., Shepson, P. B., Thompson, C. R., Pratt, K. A.,
Li, B., Peterson, P. K., Walsh, S. J., Simpson, W. R., Matrai, P. A.,
Bottenheim, J. W., Netcheva, S., Perovich, D. K., and Richter, A.: Temporal
and spatial characteristics of ozone depletion events from measurements in
the Arctic, Atmos. Chem. Phys., 14, 4875–4894,
https://doi.org/10.5194/acp-14-4875-2014, 2014.
Hall, J. S. and Wolff, E. W.: Causes of seasonal and daily variations in
aerosol sea-salt concentrations at a coastal Antarctic station, Atmos.
Environ., 32, 3669–3677, https://doi.org/10.1016/S1352-2310(98)00090-9, 1998.
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.
Hara, K., Osada, K., Matsunaga, K., Iwasaka, Y., Shibata, T., and Fuyura,
K.: Atmospheric inorganic chlorine and bromine species in Arctic boundary
layer of the winter/spring, J. Geophys. Res.-Atmos., 107, AAC 4-1–AAC 4-15,
https://doi.org/10.1029/2001JD001008, 2002.
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 the Antarctic regions: Compositional
differences between coastal and inland stations, J. Geophys. Res., 109,
D20208, https://doi.org/10.1029/2004JD004713, 2004.
Hara, K., Osada, K., Yabuki, M., and Yamanouchi, T.: Seasonal variation of
fractionated sea-salt particles on the Antarctic coast, Geophys. Res. Lett.,
39, L18801, https://doi.org/10.1029/2012GL052761, 2012.
Hara, K., Hayashi, M., Yabuki, M., Shiobara, M., and Nishita-Hara, C.:
Simultaneous aerosol measurements of unusual aerosol enhancement in the
troposphere over Syowa Station, Antarctica, Atmos. Chem. Phys., 14,
4169–4183, https://doi.org/10.5194/acp-14-4169-2014, 2014.
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., 105, 22825–22832, 2000.
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 concentration, J. Appl. Meteorol., 17, 1458–1465, 1978.
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.
Ito, T.: On the size distribution of semicron aerosols in the Antarctic
atmosphere, Nankyoku Shiro, 76, 1–19, National Institute of Polar Research,
Tokyo, 1982 (in Japanese, English abstract).
Ito, T.: Study of background aerosols in the Antarctic troposphere,
J.
Atmos. Chem., 3, 69–91, https://doi.org/10.1007/BF00049369, 1985.
Ito, T.: Antarctic Submicron Aerosols and Long-Range Transport of
Pollutants, Ambio, 18, 34–41, 1989.
Jaenicke, R. and Stingl, J.: Aitken particle size distribution in
Antarctica, in: Proceedings of International Conference on Aerosols and Ice
Nuclei, Budapest, University of Budapest Press, Budapest, Hungary, 1984.
Jayne, J., Leard, D., Zhang, X., Davidovits, P., Smith, K., Kolb, C., and
Worsnop, D.: Development of an aerosol mass spectrometer for size and
composition analysis of submicron particles, Aerosol Sci. Tech., 33, 49–70,
2000.
ourdain, 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,
D224645, 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., 113, D14308,
https://doi.org/10.1029/2007JD009584, 2008.
Kaleschke, L., Richter, A., Burrows, J., Afe, O., Heygster, G., Notholt, J.,
Rankin, A. M., Roscoe, H. K., Hollwedel, J., Wagner, T., and Jacobi, H.-W.:
Frost flowers on sea ice as a source of sea salt and their influence on
tropospheric halogen chemistry, Geophys. Res. Lett., 31, L16114,
https://doi.org/10.1029/2004GL020655, 2004.
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, 2013.
Kandler, K., Schutz, L., Deutscher, C., Ebert, M., Hofmann, H., Jackel, S.,
Jaenicke, R., Knippertz, P., Lieke, K., Massling, A., Petzold, A., Schladitz,
A., Weinzierl, B., Wiedensohler, A., Zorn, S., and Weinbruch, S.: Size
distribution, mass concentration, chemical and mineralogical composition and
derived optical parameters of the boundary layer aerosol at Tinfou, Morocco,
during SAMUM 2006, Tellus B, 61, 32–50,
https://doi.org/10.1111/j.1600-0889.2008.00385.x, 2009.
Laskin, A., Moffet, R. C., Gilles, M. K., Fast, J. D., Zaveri, R. A., Wang, B.,
Nigge, P., and Shutthanandan, J.: Tropospheric chemistry of internally mixed
sea salt and organic particles: Surprising reactivity of NaCl with weak
organic acids, J. Geophys. Res.-Atmos., 117, D017743,
https://doi.org/10.1029/2012JD017743, 2012.
Legrand, M. R. and Delmas, R. J.: Formation of HCl in the Antarctic
atmosphere, J. Geophys. Res.-Atmos., 93, 7153–7168,
https://doi.org/10.1029/JD093iD06p07153, 1988.
Legrand, M. R. and Wagenbach, D.: Impact of the Cerro Hudson and Pinatubo
volcanic eruptions on the Antarctic air and snow chemistry, J. Geophys. Res.,
104, 1581–1596, 1998.
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., 103, 11043–11056, https://doi.org/10.1029/97JD01976, 1998.
Legrand, M., Yang, X., Preunkert, S., and Theys, N.: Year-round records of
sea salt, gaseous, and particulate inorganic 10 bromine in the atmospheric
boundary layer at coastal (Dumont d'Urville) and central (Concordia) East
Antarctic sites, J. Geophys. Res.-Atmos., 121, 997–1023,
https://doi.org/10.1002/2015JD024066, 2016.
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, 2017.
Lehrer, E., Hönninger, G., and Platt, U.: A one dimensional model study of
the mechanism of halogen liberation and vertical transport in the polar
troposphere, Atmos. Chem. Phys., 4, 2427–2440,
https://doi.org/10.5194/acp-4-2427-2004, 2004.
Levine, J. G., Yang, X., Jones, A. E., and Wolff, E. W.: Sea salt as an ice core
proxy for past sea ice extent: A process-based model study, J. Geophys.
Res.-Atmos., 119, 5737–5756, 2014.
Li, L. and Pomeroy, J. W.: Estimates of Threshold Wind Speeds for Snow
Transport Using Meteorological Data, J. Appl. Meteorol., 36, 205–213,
https://doi.org/10.1175/1520-0450(1997)036<0205:EOTWSF>2.0.CO;2, 1997.
Lieb-Lappen, R. M. and Obbard, R. W.: The role of blowing snow in the
activation of bromine over first-year Antarctic sea ice, Atmos. Chem. Phys.,
15, 7537–7545, https://doi.org/10.5194/acp-15-7537-2015, 2015.
Liu, P. S. K., Deng, R., Smith, K. A., Williams, L. R., Jayne, J. T.,
Canagaratna, M. R., Moore, K., Onasch, T. B., Worsnop, D. R., and Deshler,
T.: Transmission Efficiency of an Aerodynamic Focusing Lens System:
Comparison of Model Calculations and Laboratory Measurements for the Aerodyne
Aerosol Mass Spectrometer, Aerosol Sci. Tech., 41, 721–733,
https://doi.org/10.1080/02786820701422278, 2007.
Maenhaut, W., Zoller, W. H., Duce, R. A., and Hoffman, G. L.: Concentration and
size distribution of particulate trace elements in the south polar
atmosphere, J. Geophys. Res., 84, 2421–2431, https://doi.org/10.1029/JC084iC05p02421,
1979.
McFiggans, G., Coe, H., Burgess, R., Allan, J., Cubison, M., Alfarra, M. R.,
Saunders, R., Saiz-Lopez, A., Plane, J. M. C., Wevill, D., Carpenter, L.,
Rickard, A. R., and Monks, P. S.: Direct evidence for coastal iodine
particles from Laminaria macroalgae – linkage to emissions of molecular
iodine, Atmos. Chem. Phys., 4, 701–713,
https://doi.org/10.5194/acp-4-701-2004, 2004.
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., 103, 10975–10990, https://doi.org/10.1029/98JD00249, 1998.
Monahan, E. C.: Sea spray as a function of low elevation wind speed, J.
Geophys. Res., 73, 1127–1137, https://doi.org/10.1029/JB073i004p01127, 1968.
Mouri, H., Nagao, I., Okada, K., Koga, S., and Tanaka, H.:
Individual-particle analyses of coastal Antarctic
aerosols, Tellus, 51B, 603–611, 1999.
O'Dowd, C. and Smith, M. H.: Physicochemical properties of aerosols over the
northeast Atlantic: Evidence for wind-speed-related submicron sea-salt
aerosol production, J. Geophys. Res.-Atmos., 98, 1137–1149,
https://doi.org/10.1029/92JD02302, 1993.
O'Dowd, C. D., Geever, M., and Hill, M. K.: New particle formation:
Nucleation rates and spatial scales in the clean marine coastal environment,
Geophys. Res. Lett., 25, 1661–1664, 1998.
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,
1973.
Onasch, T. B., Trimborn, A., Fortner, E. C., Jayne, J. T., Kok, G. L.,
Williams, L. R., Davidovits, P., and Worsnop, D. R.: Soot Particle Aerosol
Mass Spectrometer: Development, Validation, and Initial Application, Aerosol
Sci. Tech., 46, 804–817, https://doi.org/10.1080/02786826.2012.663948, 2012.
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.
Prados-Roman, C., Gómez-Martín, L., Puentedura, O., Navarro-Comas, M.,
Iglesias, J., de Mingo, J. R., Pérez, M., Ochoa, H., Barlasina, M. E.,
Carbajal, G., and Yela, M.: Reactive bromine in the low troposphere of
Antarctica: estimations at two research sites, Atmos. Chem. Phys., 18,
8549–8570, https://doi.org/10.5194/acp-18-8549-2018, 2018.
Pratt, K. A., Custard, K. D., Shepson, P. B., Douglas, T. A., Pöhler, D.,
General, S., Zielcke, J., Simpson, W. R., Platt, U., Tanner, D. J., and Huey,
L. G.: Photochemical production of molecular bromine in Arctic surface
snowpacks, Nat. Geosci., 6, 351, https://doi.org/10.1038/ngeo1779, 2013.
Preunkert, S., Legrand, M., Jourdain, B., Moulin, C., Belviso, S.,
Kasamatsu, N., Fukuchi, M., and Hirawake, T.: Interannual variability of
dimethylsulfide in air and seawater and its atmospheric oxidation by-products
(methanesulfonate and sulfate) at Dumont d'Urville, coastal Antarctica
(1999–2003), J. Geophys. Res., 112, D06306, https://doi.org/10.1029/2006JD007585,
2007.
Preunkert, S., Ancellet, G., Legrand, M., Kukui, A., Kerbrat, M.,
Sarda-Esteve, R., Gros, V., and Jourdain, B.: Oxidant Production over
Antarctic Land and its Export (OPALE) project: An overview of the 2010–2011
summer campaign, J. Geophys Res., 117, D15307, https://doi.org/10.1029/2011JD017145,
2012.
Prospero, J. M., Savoie, D. L., Saltzman, E. S., and Larsen, R.: Impact of
oceanic sources of biogenic sulphur on sulphate aerosol concentrations at
Mawson, Antarctica, Nature, 350, 221–223, https://doi.org/10.1038/350221a0, 1991.
Ramacher, B., Rudolph, J., and Koppmann, R.: Hydrocarbon measurements during
tropospheric ozone depletion events: Evidence for halogen atom chemistry, J.
Geophys. Res.-Atmos., 104, 3633–3653, 1999.
Rankin, A. M. and Wolff, E. W.: A year-long record of size-segregated
aerosol composition at Halley, Antarctica, J. Geophys. Res., 108, 4775,
https://doi.org/10.1029/2003JD003993, 2003.
Rankin, A. M., Auld, V., and Wolff,
E. W.: Frost flower as a source of fractionated sea salt aerosol in the polar
regions, Geophys. Res. Lett., 27, 3469–3472, 2000.
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.
Rhodes, R. H., Yang, X., Wolff, E. W., McConnell, J. R., and Frey, M. M.: Sea
ice as a source of sea salt aerosol to Greenland ice cores: a model-based
study, Atmos. Chem. Phys., 17, 9417–9433,
https://doi.org/10.5194/acp-17-9417-2017, 2017.
Rosman, K. J. R., Chrisholm, W., Boutron, C. F., Candelone, J. P., and
Patterson, C. C.: Anthropogenic lead isotopes in Antarctica, Geophys. Res.
Lett., 21, 2669–2672, 1994.
Röthlisberger, R., Hutterli, M. A., Wolff, E. W., Mulvaney, R., Fischer, H.,
Bigler, M., Goto-Azuma, K., Hansson, M. E., Ruth, U., Siggaard-Andersen, M.
L., and Steffensen, J. P.: Nitrate in Greenland and Antarctic ice cores: a
detailed description of postdepositional processes, Ann. Glaciol., 35,
209–216, 2002.
Saiz-Lopez, A., Mahajan, A. S., Salmon, R. A., Bauguitte, S. J.-B., Jones,
A. E., Roscoe, H. K., and Plane, J. M. C.: Boundary Layer Halogens in Coastal
Antarctica, Science, 317, 348–351, https://doi.org/10.1126/science.1141408, 2007.
Saiz-Lopez, A., Plane, J. M. C., Mahajan, A. S., Anderson, P. S., Bauguitte,
S. J.-B., Jones, A. E., Roscoe, H. K., Salmon, R. A., Bloss, W. J., Lee, J.
D., and Heard, D. E.: On the vertical distribution of boundary layer halogens
over coastal Antarctica: implications for O3, HOx,
NOx and the Hg lifetime, Atmos. Chem. Phys., 8, 887–900,
https://doi.org/10.5194/acp-8-887-2008, 2008.
Salcedo, D., Onasch, T. B., Aiken, A. C., Williams, L. R., de Foy, B.,
Cubison, M. J., Worsnop, D. R., Molina, L. T., and Jimenez, J. L.:
Determination of particulate lead using aerosol mass spectrometry:
MILAGRO/MCMA-2006 observations, Atmos. Chem. Phys., 10, 5371–5389,
https://doi.org/10.5194/acp-10-5371-2010, 2010.
Sander, R., Keene, W. C., Pszenny, A. A. P., Arimoto, R., Ayers, G. P.,
Baboukas, E., Cainey, J. M., Crutzen, P. J., Duce, R. A., Hönninger, G.,
Huebert, B. J., Maenhaut, W., Mihalopoulos, N., Turekian, V. C., and Van
Dingenen, R.: Inorganic bromine in the marine boundary layer: a critical
review, Atmos. Chem. Phys., 3, 1301–1336,
https://doi.org/10.5194/acp-3-1301-2003, 2003.
Saunders, R. W. and Plane, J. M. C.: Formation Pathways and Composition of
Iodine Oxide Ultra-Fine Particles, Environ. Chem., 2, 299–303,
https://doi.org/10.1071/EN05079, 2005.
Savarino, J., Kaiser, J., Morin, S., Sigman, D. M., and Thiemens, M. H.:
Nitrogen and oxygen isotopic constraints on the origin of atmospheric nitrate
in coastal Antarctica, Atmos. Chem. Phys., 7, 1925–1945,
https://doi.org/10.5194/acp-7-1925-2007, 2007.
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.
Seefeldt, M. W., Tripoli, G. J., and Stearns, C. R.: A high-resolution
numerical simulation of the wind flow in the Ross Island region,
Antarctica, Mon. Weather Rev., 131, 435–458, 2003.
Shaw, G. E.: Considerations on the origin and properties of the Antarctic
aerosol, Rev. Geophys., 17, 1983–1998, https://doi.org/10.1029/RG017i008p01983, 1979.
Shaw, G. E.: On physical properties of aerosol at Ross Island, Antarctica,
J. Aerosol Sci., 17, 937–945, 1986.
Shaw, G. E.: Antarctic Aerosols: A review, Rev. Geophys., 26,
89–112, 1988.
Simpson, W. R., von Glasow, R., Riedel, K., Anderson, P., Ariya, P.,
Bottenheim, J., Burrows, J., Carpenter, L. J., Frieß, U., Goodsite, M.
E., Heard, D., Hutterli, M., Jacobi, H.-W., Kaleschke, L., Neff, B., Plane,
J., Platt, U., Richter, A., Roscoe, H., Sander, R., Shepson, P., Sodeau, J.,
Steffen, A., Wagner, T., and Wolff, E.: Halogens and their role in polar
boundary-layer ozone depletion, Atmos. Chem. Phys., 7, 4375–4418,
https://doi.org/10.5194/acp-7-4375-2007, 2007.
Simpson, W. R., Brown, S. S., Saiz-Lopez, A., Thornton, J. A., and von Glasow,
R.: Tropospheric Halogen Chemistry: Sources, Cycling, and Impacts, Chem.
Rev., 115, 4035–4062, https://doi.org/10.1021/cr5006638, 2015.
Sipilä, M., Sarnela, N., Jokinen, T., Henschel, H., Junninen, H.,
Kontkanen, J., Richters, S., Kangasluoma, J., Franchin, A., Peräkylä,
O., and Rissanen, M. P.: Molecular-scale evidence of aerosol particle
formation via sequential addition of HIO 3, Nature, 537, 532–534,
https://doi.org/10.1038/nature19314, 2016.
Smirnov, A., Holben, B. N., Eck, T. F., Dubovik, O., and Slutsker, I.: Effect
of wind speed on columnar aerosol optical properties at Midway Island, J.
Geophys. Res.-Atmos., 108, 4802, https://doi.org/10.1029/2003JD003879, 2003.
Virkkula, A., Teinilä, K., Hillamo, R., Kerminen, V.-M., Saarikoski, S.,
Aurela, M., Koponen, I. K., and Kulmala, M.: Chemical size distributions of
boundary layer aerosol over the Atlantic Ocean and at an Antarctic site, J.
Geophys. Res., 111, D05306, https://doi.org/10.1029/2004JD004958, 2006.
von der Weiden, S.-L., Drewnick, F., and Borrmann, S.: Particle Loss
Calculator – a new software tool for the assessment of the performance of
aerosol inlet systems, Atmos. Meas. Tech., 2, 479–494,
https://doi.org/10.5194/amt-2-479-2009, 2009.
von Glasow, R., von Kuhlmann, R., Lawrence, M. G., Platt, U., and Crutzen, P.
J.: Impact of reactive bromine chemistry in the troposphere, Atmos. Chem.
Phys., 4, 2481–2497, https://doi.org/10.5194/acp-4-2481-2004, 2004.
Voskresenskii, A. I.: Condensation nuclei in the Mirny region,
Tr. Soy. Antarkt. Eksped., 38, 194–198, 1968 (in Russian).
Wagenbach, D., Görlach, U., Moser, K., and Münnich, K. O.: Coastal
Antarctic aerosol: the seasonal pattern of its chemical composition and
radionuclide content, Tellus B, 40B, 426–436,
https://doi.org/10.1111/j.1600-0889.1988.tb00114.x, 1988.
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, 1998a.
Wagenbach, D., Legrand, M., Fischer, H., Pichlmayer, F., and Wolff, E. W.:
Atmospheric near-surface nitrate at coastal Antarctic sites, J. Geophys.
Res.-Atmos., 103, 11007–11020, https://doi.org/10.1029/97JD03364, 1998b.
Warburton, J. A.: Surface measurements of Aitken nuclei at McMurdo, Siple,
Byrd and South Pole stations, Antarct. J. US, 8, p. 236, 1973.
Weller, R., Wöltjen, J., Piel, C., Resenberg, R., Wagenbach, D.,
König-Langlo, G., and Kriews, M.: Seasonal variability of crustal and
marine trace elements in the aerosol at Neumayer station, Antarctica, Tellus
B, 60, 742–752, https://doi.org/10.1111/j.1600-0889.2008.00372.x, 2008.
Wolff, E. W., Hall, J. S., Mulvaney, R., Pasteur, E. C., Wagenbach, D.,
and Legrand, M.: Relationship between chemistry of air, fresh snow and firn
cores for aerosol species in coastal Antarctica, J. Geophys. Res., 103,
11057–11070, https://doi.org/10.1029/97JD02613, 1998.
Wouters, L., Artaxo, P., and Van Grieken, R.: Laser Microprobe Mass Analysis
of Individual Antarctic Aerosol Particles, Int. J. Environ. An. Ch., 38,
427–438, https://doi.org/10.1080/0306731900802694, 1990.
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.
Yang, X., Frey, M., Norris, S., Brooks, I., Anderson, P., Jones, A., and
Legrand, M.: Sea salt aerosol from blowing snow on sea ice-modeling vs
observation, Geophys. Res. Abstr., Vol. 18, p. 16828, EGU General Assembly
2016, Vienna, Austria, 2016.
Yang, X., Nedela, V., Runštuk, J., Ondrušková, G., Krausko, J.,
Vetráková, L., and Heger, D.: Evaporating brine from frost flowers with
electron microscopy and implications for atmospheric chemistry and sea-salt
aerosol formation, Atmos. Chem. Phys., 17, 6291–6303,
https://doi.org/10.5194/acp-17-6291-2017, 2017.
Zorn, S. R., Drewnick, F., Schott, M., Hoffmann, T., and Borrmann, S.:
Characterization of the South Atlantic marine boundary layer aerosol using an
aerodyne aerosol mass spectrometer, Atmos. Chem. Phys., 8, 4711–4728,
https://doi.org/10.5194/acp-8-4711-2008, 2008.
Short summary
The 2ODIAC field campaign was the first deployment of a high-resolution, real-time mass spectrometer to continental Antarctica. Using the real-time aerosol measurements, we investigate how the composition of Antarctic submicron aerosol changes as a function of meteorological parameters such as wind speed. We observe blowing snow and increasing aerosol concentration and changing composition, in particular halogens, as the wind increases beyond 8 m s−1.
The 2ODIAC field campaign was the first deployment of a high-resolution, real-time mass...
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