Articles | Volume 18, issue 16
https://doi.org/10.5194/acp-18-12595-2018
© 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-18-12595-2018
© Author(s) 2018. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
The diverse chemical mixing state of aerosol particles in the southeastern United States
Amy L. Bondy
Department of Chemistry, University of Michigan, Ann Arbor, MI 48109,
USA
Daniel Bonanno
Department of Chemistry, University of the Pacific, Stockton, CA
95211, USA
Ryan C. Moffet
Department of Chemistry, University of the Pacific, Stockton, CA
95211, USA
Bingbing Wang
Environmental Molecular Sciences Laboratory, Pacific Northwest
National Laboratory, Richland, WA 99354, USA
present address: State Key Laboratory of Marine Environmental Science,
College of Ocean and Earth Sciences, Xiamen University, Xiamen, China
Alexander Laskin
Environmental Molecular Sciences Laboratory, Pacific Northwest
National Laboratory, Richland, WA 99354, USA
present address: Department of Chemistry, Purdue University, West
Lafayette, IN 47907, USA
Department of Chemistry, University of Michigan, Ann Arbor, MI 48109,
USA
Department of Environmental Health Sciences, University of Michigan,
Ann Arbor, MI 48109, USA
Related authors
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
Short summary
Short summary
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.
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
Short summary
Short summary
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.
Feng Jiang, Kyla Siemens, Claudia Linke, Yanxia Li, Yiwei Gong, Thomas Leisner, Alexander Laskin, and Harald Saathoff
Atmos. Chem. Phys., 24, 2639–2649, https://doi.org/10.5194/acp-24-2639-2024, https://doi.org/10.5194/acp-24-2639-2024, 2024
Short summary
Short summary
We investigated the optical properties, chemical composition, and formation mechanisms of secondary organic aerosol (SOA) and brown carbon (BrC) from the oxidation of indole with and without NO2 in the Aerosol Interaction and Dynamics in the Atmosphere (AIDA) simulation chamber. This work is one of the very few to link the optical properties and chemical composition of indole SOA with and without NO2 by simulation chamber experiments.
Daniel A. Knopf, Peiwen Wang, Benny Wong, Jay M. Tomlin, Daniel P. Veghte, Nurun N. Lata, Swarup China, Alexander Laskin, Ryan C. Moffet, Josephine Y. Aller, Matthew A. Marcus, and Jian Wang
Atmos. Chem. Phys., 23, 8659–8681, https://doi.org/10.5194/acp-23-8659-2023, https://doi.org/10.5194/acp-23-8659-2023, 2023
Short summary
Short summary
Ambient particle populations and associated ice-nucleating particles (INPs)
were examined from particle samples collected on board aircraft in the marine
boundary layer and free troposphere in the eastern North Atlantic during
summer and winter. Chemical imaging shows distinct differences in the
particle populations seasonally and with sampling altitudes, which are
reflected in the INP types. Freezing parameterizations are derived for
implementation in cloud-resolving and climate models.
Haley M. Royer, Mira L. Pöhlker, Ovid Krüger, Edmund Blades, Peter Sealy, Nurun Nahar Lata, Zezhen Cheng, Swarup China, Andrew P. Ault, Patricia K. Quinn, Paquita Zuidema, Christopher Pöhlker, Ulrich Pöschl, Meinrat Andreae, and Cassandra J. Gaston
Atmos. Chem. Phys., 23, 981–998, https://doi.org/10.5194/acp-23-981-2023, https://doi.org/10.5194/acp-23-981-2023, 2023
Short summary
Short summary
This paper presents atmospheric particle chemical composition and measurements of aerosol water uptake properties collected at Ragged Point, Barbados, during the winter of 2020. The result of this study indicates the importance of small African smoke particles for cloud droplet formation in the tropical North Atlantic and highlights the large spatial and temporal pervasiveness of smoke over the Atlantic Ocean.
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
Short summary
Short summary
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.
Daniel A. Knopf, Joseph C. Charnawskas, Peiwen Wang, Benny Wong, Jay M. Tomlin, Kevin A. Jankowski, Matthew Fraund, Daniel P. Veghte, Swarup China, Alexander Laskin, Ryan C. Moffet, Mary K. Gilles, Josephine Y. Aller, Matthew A. Marcus, Shira Raveh-Rubin, and Jian Wang
Atmos. Chem. Phys., 22, 5377–5398, https://doi.org/10.5194/acp-22-5377-2022, https://doi.org/10.5194/acp-22-5377-2022, 2022
Short summary
Short summary
Marine boundary layer aerosols collected in the remote region of the eastern North Atlantic induce immersion freezing and deposition ice nucleation under typical mixed-phase and cirrus cloud conditions. Corresponding ice nucleation parameterizations for model applications have been derived. Chemical imaging of ambient aerosol and ice-nucleating particles demonstrates that the latter is dominated by sea salt and organics while also representing a major particle type in the particle population.
Jay M. Tomlin, Kevin A. Jankowski, Daniel P. Veghte, Swarup China, Peiwen Wang, Matthew Fraund, Johannes Weis, Guangjie Zheng, Yang Wang, Felipe Rivera-Adorno, Shira Raveh-Rubin, Daniel A. Knopf, Jian Wang, Mary K. Gilles, Ryan C. Moffet, and Alexander Laskin
Atmos. Chem. Phys., 21, 18123–18146, https://doi.org/10.5194/acp-21-18123-2021, https://doi.org/10.5194/acp-21-18123-2021, 2021
Short summary
Short summary
Analysis of individual atmospheric particles shows that aerosol transported from North America during meteorological dry intrusion episodes may have a substantial impact on the mixing state and particle-type population over the mid-Atlantic, as organic contribution and particle-type diversity are significantly enhanced during these periods. These observations need to be considered in current atmospheric models.
Yang Wang, Guangjie Zheng, Michael P. Jensen, Daniel A. Knopf, Alexander Laskin, Alyssa A. Matthews, David Mechem, Fan Mei, Ryan Moffet, Arthur J. Sedlacek, John E. Shilling, Stephen Springston, Amy Sullivan, Jason Tomlinson, Daniel Veghte, Rodney Weber, Robert Wood, Maria A. Zawadowicz, and Jian Wang
Atmos. Chem. Phys., 21, 11079–11098, https://doi.org/10.5194/acp-21-11079-2021, https://doi.org/10.5194/acp-21-11079-2021, 2021
Short summary
Short summary
This paper reports the vertical profiles of trace gas and aerosol properties over the eastern North Atlantic, a region of persistent but diverse subtropical marine boundary layer (MBL) clouds. We examined the key processes that drive the cloud condensation nuclei (CCN) population and how it varies with season and synoptic conditions. This study helps improve the model representation of the aerosol processes in the remote MBL, reducing the simulated aerosol indirect effects.
Yue Zhou, Christopher P. West, Anusha P. S. Hettiyadura, Xiaoying Niu, Hui Wen, Jiecan Cui, Tenglong Shi, Wei Pu, Xin Wang, and Alexander Laskin
Atmos. Chem. Phys., 21, 8531–8555, https://doi.org/10.5194/acp-21-8531-2021, https://doi.org/10.5194/acp-21-8531-2021, 2021
Short summary
Short summary
We present a comprehensive characterization of water-soluble organic carbon (WSOC) in seasonal snow of northwestern China. We applied complementary multimodal analytical techniques to investigate bulk and molecular-level composition, optical properties, and sources of WSOC. For the first time, we estimated the extent of radiative forcing due to WSOC in snow using a model simulation and showed the profound influences of WSOC on the energy budget of midlatitude seasonal snowpack.
Demetrios Pagonis, Pedro Campuzano-Jost, Hongyu Guo, Douglas A. Day, Melinda K. Schueneman, Wyatt L. Brown, Benjamin A. Nault, Harald Stark, Kyla Siemens, Alex Laskin, Felix Piel, Laura Tomsche, Armin Wisthaler, Matthew M. Coggon, Georgios I. Gkatzelis, Hannah S. Halliday, Jordan E. Krechmer, Richard H. Moore, David S. Thomson, Carsten Warneke, Elizabeth B. Wiggins, and Jose L. Jimenez
Atmos. Meas. Tech., 14, 1545–1559, https://doi.org/10.5194/amt-14-1545-2021, https://doi.org/10.5194/amt-14-1545-2021, 2021
Short summary
Short summary
We describe the airborne deployment of an extractive electrospray time-of-flight mass spectrometer (EESI-MS). The instrument provides a quantitative 1 Hz measurement of the chemical composition of organic aerosol up to altitudes of
7 km, with single-compound detection limits as low as 50 ng per standard cubic meter.
Ana C. Morales, Thilina Jayarathne, Jonathan H. Slade, Alexander Laskin, and Paul B. Shepson
Atmos. Chem. Phys., 21, 129–145, https://doi.org/10.5194/acp-21-129-2021, https://doi.org/10.5194/acp-21-129-2021, 2021
Short summary
Short summary
Organic nitrates formed from the oxidation of biogenic volatile organic compounds impact both ozone and particulate matter as they remove nitrogen oxides, but they represent important aerosol precursors. We conducted a series of reaction chamber experiments that quantified the total organic nitrate and secondary organic aerosol yield from the OH-radical-initiated oxidation of ocimene, and also measured their hydrolysis lifetimes in the aqueous phase, as a function of pH.
Matthew Fraund, Daniel J. Bonanno, Swarup China, Don Q. Pham, Daniel Veghte, Johannes Weis, Gourihar Kulkarni, Ken Teske, Mary K. Gilles, Alexander Laskin, and Ryan C. Moffet
Atmos. Chem. Phys., 20, 11593–11606, https://doi.org/10.5194/acp-20-11593-2020, https://doi.org/10.5194/acp-20-11593-2020, 2020
Short summary
Short summary
High viscosity organic particles (HVOPs) in the Southern Great Plains have been analyzed, and two particle types were found. Previously studied tar balls and the recently discovered airborne soil organic particles (ASOPs) are both shown to be brown carbon (BrC). These particle types can be identified in bulk by an absorption Ångström exponent approaching 2.6. HVOP types can be differentiated by comparing carbon absorption spectrum peak ratios between the carboxylic acid, alcohol, and sp2 peaks.
Havala O. T. Pye, Athanasios Nenes, Becky Alexander, Andrew P. Ault, Mary C. Barth, Simon L. Clegg, Jeffrey L. Collett Jr., Kathleen M. Fahey, Christopher J. Hennigan, Hartmut Herrmann, Maria Kanakidou, James T. Kelly, I-Ting Ku, V. Faye McNeill, Nicole Riemer, Thomas Schaefer, Guoliang Shi, Andreas Tilgner, John T. Walker, Tao Wang, Rodney Weber, Jia Xing, Rahul A. Zaveri, and Andreas Zuend
Atmos. Chem. Phys., 20, 4809–4888, https://doi.org/10.5194/acp-20-4809-2020, https://doi.org/10.5194/acp-20-4809-2020, 2020
Short summary
Short summary
Acid rain is recognized for its impacts on human health and ecosystems, and programs to mitigate these effects have had implications for atmospheric acidity. Historical measurements indicate that cloud and fog droplet acidity has changed in recent decades in response to controls on emissions from human activity, while the limited trend data for suspended particles indicate acidity may be relatively constant. This review synthesizes knowledge on the acidity of atmospheric particles and clouds.
Lauren T. Fleming, Peng Lin, James M. Roberts, Vanessa Selimovic, Robert Yokelson, Julia Laskin, Alexander Laskin, and Sergey A. Nizkorodov
Atmos. Chem. Phys., 20, 1105–1129, https://doi.org/10.5194/acp-20-1105-2020, https://doi.org/10.5194/acp-20-1105-2020, 2020
Short summary
Short summary
We have explored the nature and stability of molecules that give biomass burning smoke its faint brown color. Different types of biomass fuels were burned and the resulting smoke was collected for a detailed chemical analysis. We found that brown molecules in smoke become less colored when they are irradiated by sunlight, but this photobleaching process is very slow. This means that biomass burning smoke will remain brown-colored for a long time and efficiently warm up the atmosphere.
Mijung Song, Adrian M. Maclean, Yuanzhou Huang, Natalie R. Smith, Sandra L. Blair, Julia Laskin, Alexander Laskin, Wing-Sy Wong DeRieux, Ying Li, Manabu Shiraiwa, Sergey A. Nizkorodov, and Allan K. Bertram
Atmos. Chem. Phys., 19, 12515–12529, https://doi.org/10.5194/acp-19-12515-2019, https://doi.org/10.5194/acp-19-12515-2019, 2019
Weijun Li, Lei Liu, Qi Yuan, Liang Xu, Yanhong Zhu, Bingbing Wang, Hua Yu, Xiaokun Ding, Jian Zhang, Dao Huang, Dantong Liu, Wei Hu, Daizhou Zhang, Pingqing Fu, Maosheng Yao, Min Hu, Xiaoye Zhang, and Zongbo Shi
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2019-539, https://doi.org/10.5194/acp-2019-539, 2019
Preprint withdrawn
Short summary
Short summary
The real state of individual primary biological aerosol particles (PBAPs) derived from natural sources is under mystery, although many studies well evaluate the morphology, mixing state, and elemental composition of anthropogenic particles. It induces that some studies mislead some anthropogenic particles into biological particles through electron microscopy. Here we firstly estimate the full database of individual PBAPs through two microscopic instruments. The database is good for research.
Matthew Fraund, Tim Park, Lin Yao, Daniel Bonanno, Don Q. Pham, and Ryan C. Moffet
Atmos. Meas. Tech., 12, 1619–1633, https://doi.org/10.5194/amt-12-1619-2019, https://doi.org/10.5194/amt-12-1619-2019, 2019
Short summary
Short summary
Scanning transmission X-ray microscopy (STXM) is a powerful tool which is able to determine the elemental and functional composition of aerosols on a subparticle level. The current work validates the use of STXM for quantitatively calculating the organic volume fraction of individual aerosols by applying the calculation to lab-prepared samples. The caveats and limitations for this calculation are shown as well.
Victoria E. Irish, Sarah J. Hanna, Megan D. Willis, Swarup China, Jennie L. Thomas, Jeremy J. B. Wentzell, Ana Cirisan, Meng Si, W. Richard Leaitch, Jennifer G. Murphy, Jonathan P. D. Abbatt, Alexander Laskin, Eric Girard, and Allan K. Bertram
Atmos. Chem. Phys., 19, 1027–1039, https://doi.org/10.5194/acp-19-1027-2019, https://doi.org/10.5194/acp-19-1027-2019, 2019
Short summary
Short summary
Ice nucleating particles (INPs) are atmospheric particles that catalyse the formation of ice crystals in clouds. INPs influence the Earth's radiative balance and hydrological cycle. In this study we measured the concentrations of INPs in the Canadian Arctic marine boundary layer. Average INP concentrations fell within the range measured in other marine boundary layer locations. We also found that mineral dust is a more important contributor to the INP population than sea spray aerosol.
Chunlin Li, Quanfu He, Julian Schade, Johannes Passig, Ralf Zimmermann, Daphne Meidan, Alexander Laskin, and Yinon Rudich
Atmos. Chem. Phys., 19, 139–163, https://doi.org/10.5194/acp-19-139-2019, https://doi.org/10.5194/acp-19-139-2019, 2019
Wing-Sy Wong DeRieux, Ying Li, Peng Lin, Julia Laskin, Alexander Laskin, Allan K. Bertram, Sergey A. Nizkorodov, and Manabu Shiraiwa
Atmos. Chem. Phys., 18, 6331–6351, https://doi.org/10.5194/acp-18-6331-2018, https://doi.org/10.5194/acp-18-6331-2018, 2018
Short summary
Short summary
The phase transition of organic particles between glassy and semi-solid states occurs at the glass transition temperature. We developed a method to predict glass transition temperatures and the viscosity of secondary organic aerosols using molecular composition, with consistent results with viscosity measurements. The viscosity of biomass burning particles was also estimated using the chemical composition measured by high-resolution mass spectrometry with two different ionization techniques.
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
Short summary
Short summary
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
Short summary
Short summary
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.
Lauren T. Fleming, Peng Lin, Alexander Laskin, Julia Laskin, Robert Weltman, Rufus D. Edwards, Narendra K. Arora, Ankit Yadav, Simone Meinardi, Donald R. Blake, Ajay Pillarisetti, Kirk R. Smith, and Sergey A. Nizkorodov
Atmos. Chem. Phys., 18, 2461–2480, https://doi.org/10.5194/acp-18-2461-2018, https://doi.org/10.5194/acp-18-2461-2018, 2018
Short summary
Short summary
Household cooking emissions in India, which rely on traditional meal preparation with dung- and brushwood-fueled cookstoves, produce copious amounts of particulate matter. Detailed chemical analysis of the compounds found in this particulate matter detected a large number of previously unidentified nitrogen-containing organic compounds, originating from dung-fueled cookstoves.
Mallory L. Hinks, Julia Montoya-Aguilera, Lucas Ellison, Peng Lin, Alexander Laskin, Julia Laskin, Manabu Shiraiwa, Donald Dabdub, and Sergey A. Nizkorodov
Atmos. Chem. Phys., 18, 1643–1652, https://doi.org/10.5194/acp-18-1643-2018, https://doi.org/10.5194/acp-18-1643-2018, 2018
Short summary
Short summary
We have observed a strong effect of relative humidity on the composition of particulate matter produced from the oxidation of toluene in clean air. At higher relative humidity, there was a significant reduction in the fraction of high-molecular-weight compounds present in the particles. The amount of particulate matter also decreased at higher relative humidity. The main implication of this study is that water vapor participates in the photooxidation of toluene in a complicated way.
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
Short summary
Short summary
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.
Julia Montoya-Aguilera, Jeremy R. Horne, Mallory L. Hinks, Lauren T. Fleming, Véronique Perraud, Peng Lin, Alexander Laskin, Julia Laskin, Donald Dabdub, and Sergey A. Nizkorodov
Atmos. Chem. Phys., 17, 11605–11621, https://doi.org/10.5194/acp-17-11605-2017, https://doi.org/10.5194/acp-17-11605-2017, 2017
Short summary
Short summary
Various plant species emit a chemical compound called indole under stressed conditions or during flowering events. Our experiments show that indole can be oxidized in the atmosphere to produce a brownish haze containing well-known indole-derived dyes, such as indigo dye. An airshed model that includes indole chemistry shows that indole aerosol makes a significant contribution to the total aerosol burden and to visibility.
Yevgeny Derimian, Marie Choël, Yinon Rudich, Karine Deboudt, Oleg Dubovik, Alexander Laskin, Michel Legrand, Bahaiddin Damiri, Ilan Koren, Florin Unga, Myriam Moreau, Meinrat O. Andreae, and Arnon Karnieli
Atmos. Chem. Phys., 17, 11331–11353, https://doi.org/10.5194/acp-17-11331-2017, https://doi.org/10.5194/acp-17-11331-2017, 2017
Short summary
Short summary
We present influence of daily occurrence of the sea breeze flow from the Mediterranean Sea on physicochemical and optical properties of atmospheric aerosol deep inland in the Negev Desert of Israel. Sampled airborne dust was found be internally mixed with sea-salt particles and reacted with anthropogenic pollution, which makes the dust highly hygroscopic and a liquid coating of particles appears. These physicochemical transformations are associated with a change in aerosol radiative properties.
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
Short summary
Short summary
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.
Adam P. Bateman, Zhaoheng Gong, Tristan H. Harder, Suzane S. de Sá, Bingbing Wang, Paulo Castillo, Swarup China, Yingjun Liu, Rachel E. O'Brien, Brett B. Palm, Hung-Wei Shiu, Glauber G. Cirino, Ryan Thalman, Kouji Adachi, M. Lizabeth Alexander, Paulo Artaxo, Allan K. Bertram, Peter R. Buseck, Mary K. Gilles, Jose L. Jimenez, Alexander Laskin, Antonio O. Manzi, Arthur Sedlacek, Rodrigo A. F. Souza, Jian Wang, Rahul Zaveri, and Scot T. Martin
Atmos. Chem. Phys., 17, 1759–1773, https://doi.org/10.5194/acp-17-1759-2017, https://doi.org/10.5194/acp-17-1759-2017, 2017
Short summary
Short summary
The occurrence of nonliquid and liquid physical states of submicron atmospheric particulate matter (PM) downwind of an urban region in central Amazonia was investigated. Air masses representing background conditions, urban pollution, and regional- and continental-scale biomass were measured. Anthropogenic influences contributed to the presence of nonliquid PM in the atmospheric particle population, while liquid PM dominated during periods of biogenic influence.
Ryan C. Moffet, Rachel E. O'Brien, Peter A. Alpert, Stephen T. Kelly, Don Q. Pham, Mary K. Gilles, Daniel A. Knopf, and Alexander Laskin
Atmos. Chem. Phys., 16, 14515–14525, https://doi.org/10.5194/acp-16-14515-2016, https://doi.org/10.5194/acp-16-14515-2016, 2016
Short summary
Short summary
Atmospheric black carbon (BC), commonly known as soot, is an important constituent of the earth that imparts a warming similar to that of carbon dioxide. However, BC is much shorter lived and has uncertain warming due to its mixture with other solid and liquid components. Here, advanced microscopic methods have provided a detailed look at thousands of BC particles sampled from central California; these measurements will lead towards a better understanding of the effects that BC has on climate.
Jiumeng Liu, Peng Lin, Alexander Laskin, Julia Laskin, Shawn M. Kathmann, Matthew Wise, Ryan Caylor, Felisha Imholt, Vanessa Selimovic, and John E. Shilling
Atmos. Chem. Phys., 16, 12815–12827, https://doi.org/10.5194/acp-16-12815-2016, https://doi.org/10.5194/acp-16-12815-2016, 2016
Short summary
Short summary
Light absorbing organic aerosols (BrC) absorb sunlight thereby influencing climate; however, understanding of the link between their optical properties and environmental variables remains limited. Our chamber experiment results suggest that variables including NOx concentration, RH level, and photolysis time have considerable influence on secondary BrC optical properties. The results contribute to a more accurate characterization of the impacts of aerosols on climate, especially in urban areas.
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
Short summary
Short summary
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.
Lu Yu, Jeremy Smith, Alexander Laskin, Katheryn M. George, Cort Anastasio, Julia Laskin, Ann M. Dillner, and Qi Zhang
Atmos. Chem. Phys., 16, 4511–4527, https://doi.org/10.5194/acp-16-4511-2016, https://doi.org/10.5194/acp-16-4511-2016, 2016
Short summary
Short summary
The chemical evolution of SOA formed during aqueous reactions of phenolic compounds is studied via combined bulk and molecular analysis. Phenolic SOA evolve dynamically during photochemical aging, with different reaction mechanisms (oligomerization, fragmentation, and functionalization) leading to different generations of products that span an enormous range in volatilities and a large range in oxidation state and composition. Aqueous reactions of phenols are likely an important source of ELVOC.
H. M. Allen, D. C. Draper, B. R. Ayres, A. Ault, A. Bondy, S. Takahama, R. L. Modini, K. Baumann, E. Edgerton, C. Knote, A. Laskin, B. Wang, and J. L. Fry
Atmos. Chem. Phys., 15, 10669–10685, https://doi.org/10.5194/acp-15-10669-2015, https://doi.org/10.5194/acp-15-10669-2015, 2015
Short summary
Short summary
We report ion chromatographic measurements of gas- and aerosol-phase inorganic species at the SOAS 2013 field study. Our particular focus is on inorganic nitrate aerosol formation via HNO3 uptake onto coarse-mode dust and sea salt particles, which we find to be the dominant source of episodic inorganic nitrate at this site, due to the high acidity of the particles preventing formation of NH4NO3. We calculate a production rate of inorganic nitrate aerosol.
J. M. Creamean, A. P. Ault, A. B. White, P. J. Neiman, F. M. Ralph, P. Minnis, and K. A. Prather
Atmos. Chem. Phys., 15, 6535–6548, https://doi.org/10.5194/acp-15-6535-2015, https://doi.org/10.5194/acp-15-6535-2015, 2015
Short summary
Short summary
Aerosols impact how clouds and precipitation form. In the California Sierra Nevada, we found that the formation and resulting amount of rain and snow were impacted by mineral dust, bioparticles such as bacteria, and biomass burning and pollution particles during three winter seasons. Dust and bioparticles from distant sources impacted high-altitude clouds by forming ice, leading to more precipitation, whereas local biomass burning and pollution entered the base of clouds, leading to less rain.
R. C. Moffet, T. C. Rödel, S. T. Kelly, X. Y. Yu, G. T. Carroll, J. Fast, R. A. Zaveri, A. Laskin, and M. K. Gilles
Atmos. Chem. Phys., 13, 10445–10459, https://doi.org/10.5194/acp-13-10445-2013, https://doi.org/10.5194/acp-13-10445-2013, 2013
Related subject area
Subject: Aerosols | Research Activity: Field Measurements | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Bridging gas and aerosol properties between the northeastern US and Bermuda: analysis of eight transit flights
The behaviour of charged particles (ions) during new particle formation events in urban Leipzig, Germany
Exploring the sources of light-absorbing carbonaceous aerosols by integrating observational and modeling results: insights from Northeast China
Measurement report: Characteristics of airborne black-carbon-containing particles during the 2021 summer COVID-19 lockdown in a typical Yangtze River Delta city, China
Aerosol optical properties within the atmospheric boundary layer predicted from ground-based observations compared to Raman lidar retrievals during RITA-2021
Hygroscopic growth and activation changed submicron aerosol composition and properties in the North China Plain
Measurement report: Formation of tropospheric brown carbon in a lifting air mass
Vertical variability of aerosol properties and trace gases over a remote marine region: a case study over Bermuda
Differences in aerosol and cloud properties along the central California coast when winds change from northerly to southerly
International airport emissions and their impact on local air quality: chemical speciation of ambient aerosols at Madrid–Barajas Airport during the AVIATOR campaign
The local ship speed reduction effect on black carbon emissions measured at a remote marine station
High-altitude aerosol chemical characterization and source identification: insights from the CALISHTO campaign
Measurement report: Impact of emission control measures on environmental persistent free radicals and reactive oxygen species – a short-term case study in Beijing
Characterizing water solubility of fresh and aged secondary organic aerosol in PM2.5 with the stable carbon isotope technique
Measurement report: Impact of cloud processes on secondary organic aerosols at a forested mountain site in southeastern China
Critical contribution of chemically diverse carbonyl molecules to the oxidative potential of atmospheric aerosols
Measurement report: Vanadium-containing ship exhaust particles detected in and above the marine boundary layer in the remote atmosphere
Diverging trends in aerosol sulfate and nitrate measured in the remote North Atlantic in Barbados are attributed to clean air policies, African smoke, and anthropogenic emissions
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
Automated compound speciation, cluster analysis, and quantification of organic vapours and aerosols using comprehensive two-dimensional gas chromatography and mass spectrometry
Atmospheric evolution of environmentally persistent free radicals in rural North China Plain: insights into water solubility and effects on PM2.5 oxidative potential
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
A Multi-site Passive Approach for Studying the Emissions and Evolution of Smoke from Prescribed Fires
Simultaneous organic aerosol source apportionment at two Antarctic sites reveals large-scale and ecoregion-specific components
Two distinct ship emission profiles for organic-sulfate source apportionment of PM in sulfur emission control areas
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
Primary and secondary emissions from a modern fleet of city buses
Dominant Influence of Biomass Combustion and Cross-Border Transport on Nitrogen-Containing Organic Compound Levels in the Southeastern Tibetan Plateau
Measurement report: Characteristics of aminiums in PM2.5 during winter clean and polluted episodes in China: aminium outbreak and its constraint
Impact assessment of terrestrial and marine air-mass on the constituents and intermixing of bioaerosols over coastal atmosphere
Assessing the influence of long-range transport of aerosols on the PM2.5 chemical composition and concentration in the Aburrá Valley
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: Bio-physicochemistry of tropical clouds at Maïdo (Réunion, Indian Ocean): overview of results from the BIO-MAÏDO campaign
Impacts of elevated anthropogenic emissions on physicochemical characteristics of BC-containing particles over the Tibetan Plateau
Chemical properties and single-particle mixing state of soot aerosol in Houston during the TRACER campaign
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
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
Cassidy Soloff, Taiwo Ajayi, Yonghoon Choi, Ewan C. Crosbie, Joshua P. DiGangi, Glenn S. Diskin, Marta A. Fenn, Richard A. Ferrare, Francesca Gallo, Johnathan W. Hair, Miguel Ricardo A. Hilario, Simon Kirschler, Richard H. Moore, Taylor J. Shingler, Michael A. Shook, Kenneth L. Thornhill, Christiane Voigt, Edward L. Winstead, Luke D. Ziemba, and Armin Sorooshian
Atmos. Chem. Phys., 24, 10385–10408, https://doi.org/10.5194/acp-24-10385-2024, https://doi.org/10.5194/acp-24-10385-2024, 2024
Short summary
Short summary
Using aircraft measurements over the northwestern Atlantic between the US East Coast and Bermuda and trajectory modeling of continental outflow, we identify trace gas and particle properties that exhibit gradients with offshore distance and quantify these changes with high-resolution measurements of concentrations and particle chemistry, size, and scattering properties. This work furthers our understanding of the complex interactions between continental and marine environments.
Alex Rowell, James Brean, David C. S. Beddows, Zongbo Shi, Avinash Kumar, Matti Rissanen, Miikka Dal Maso, Peter Mettke, Kay Weinhold, Maik Merkel, and Roy M. Harrison
Atmos. Chem. Phys., 24, 10349–10361, https://doi.org/10.5194/acp-24-10349-2024, https://doi.org/10.5194/acp-24-10349-2024, 2024
Short summary
Short summary
Ions enhance the formation and growth rates of new particles, affecting the Earth's radiation budget. Despite these effects, there is little published data exploring the sources of ions in the urban environment and their role in new particle formation (NPF). Here we show that natural ion sources dominate in urban environments, while traffic is a secondary source. Ions contribute up to 12.7 % of the formation rate of particles, indicating that they are important for forming urban PM.
Yuan Cheng, Xu-bing Cao, Sheng-qiang Zhu, Zhi-qing Zhang, Jiu-meng Liu, Hong-liang Zhang, Qiang Zhang, and Ke-bin He
Atmos. Chem. Phys., 24, 9869–9883, https://doi.org/10.5194/acp-24-9869-2024, https://doi.org/10.5194/acp-24-9869-2024, 2024
Short summary
Short summary
The agreement between observational and modeling results is essential for the development of efficient air pollution control strategies. Here we constrained the modeling results of carbonaceous aerosols by field observation in Northeast China, a historically overlooked but recently targeted region of national clean-air actions. Our study suggested that the simulation of agricultural fire emissions and secondary organic aerosols remains challenging.
Yuan Dai, Junfeng Wang, Houjun Wang, Shijie Cui, Yunjiang Zhang, Haiwei Li, Yun Wu, Ming Wang, Eleonora Aruffo, and Xinlei Ge
Atmos. Chem. Phys., 24, 9733–9748, https://doi.org/10.5194/acp-24-9733-2024, https://doi.org/10.5194/acp-24-9733-2024, 2024
Short summary
Short summary
Short-term strict emission control can improve air quality, but its effectiveness needs assessment. During the 2021 summer COVID-19 lockdown in Yangzhou, we found that PM2.5 levels did not decrease despite reduced primary emissions. Aged black-carbon particles increased substantially due to higher O3 levels and transported pollutants. High humidity and low wind also played key roles. The results highlight the importance of a regionally balanced control strategy for future air quality management.
Xinya Liu, Diego Alves Gouveia, Bas Henzing, Arnoud Apituley, Arjan Hensen, Danielle van Dinther, Rujin Huang, and Ulrike Dusek
Atmos. Chem. Phys., 24, 9597–9614, https://doi.org/10.5194/acp-24-9597-2024, https://doi.org/10.5194/acp-24-9597-2024, 2024
Short summary
Short summary
The vertical distribution of aerosol optical properties is important for their effect on climate. This is usually measured by lidar, which has limitations, most notably the assumption of a lidar ratio. Our study shows that routine surface-level aerosol measurements are able to predict this lidar ratio reasonably well within the lower layers of the atmosphere and thus provide a relatively simple and cost-effective method to improve lidar measurements.
Weiqi Xu, Ye Kuang, Wanyun Xu, Zhiqiang Zhang, Biao Luo, Xiaoyi Zhang, Jiangchuang Tao, Hongqin Qiao, Li Liu, and Yele Sun
Atmos. Chem. Phys., 24, 9387–9399, https://doi.org/10.5194/acp-24-9387-2024, https://doi.org/10.5194/acp-24-9387-2024, 2024
Short summary
Short summary
We deployed an advanced aerosol–fog sampling system at a rural site in the North China Plain to investigate impacts of aerosol hygroscopic growth and activation on the physicochemical properties of submicron aerosols. Observed results highlighted remarkably different aqueous processing of primary and secondary submicron aerosol components under distinct ambient relative humidity (RH) conditions and that RH levels significantly impact aerosol sampling through the aerosol swelling effect.
Can Wu, Xiaodi Liu, Ke Zhang, Si Zhang, Cong Cao, Jianjun Li, Rui Li, Fan Zhang, and Gehui Wang
Atmos. Chem. Phys., 24, 9263–9275, https://doi.org/10.5194/acp-24-9263-2024, https://doi.org/10.5194/acp-24-9263-2024, 2024
Short summary
Short summary
Brown carbon (BrC) is prevalent in the troposphere and can efficiently absorb solar and terrestrial radiation. Our observations show 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.
Taiwo 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 D. Ziemba, and Armin Sorooshian
Atmos. Chem. Phys., 24, 9197–9218, https://doi.org/10.5194/acp-24-9197-2024, https://doi.org/10.5194/acp-24-9197-2024, 2024
Short summary
Short summary
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 the vertical dependence of trace gas and aerosol properties.
Kira Zeider, Grace Betito, Anthony Bucholtz, Peng Xian, Annette Walker, and Armin Sorooshian
Atmos. Chem. Phys., 24, 9059–9083, https://doi.org/10.5194/acp-24-9059-2024, https://doi.org/10.5194/acp-24-9059-2024, 2024
Short summary
Short summary
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 and continental sources, and clouds had more but smaller droplets.
Saleh Alzahrani, Doğuşhan Kılıç, Michael Flynn, Paul I. Williams, and James Allan
Atmos. Chem. Phys., 24, 9045–9058, https://doi.org/10.5194/acp-24-9045-2024, https://doi.org/10.5194/acp-24-9045-2024, 2024
Short summary
Short summary
This paper investigates emissions from aviation activities at an international airport to evaluate their impact on local air quality. The study provides detailed insights into the chemical composition of aerosols and key pollutants in the airport environment. Source apportionment analysis using positive matrix factorisation (PMF) identified three significant sources: less oxidised oxygenated organic aerosol, alkane organic aerosol, and more oxidised oxygenated organic aerosol.
Mikko Heikkilä, Krista Luoma, Timo Mäkelä, and Tiia Grönholm
Atmos. Chem. Phys., 24, 8927–8941, https://doi.org/10.5194/acp-24-8927-2024, https://doi.org/10.5194/acp-24-8927-2024, 2024
Short summary
Short summary
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 per kilogram of fuel. Ships with an exhaust gas cleaning system (EGCS) were found to have median BC emissions per fuel consumed 5 times lower than ships without an EGCS. However, this might be because of non-EGCS ships running at low engine loads rather than the EGCS itself. A local speed restriction would increase BC emissions of ships.
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
Atmos. Chem. Phys., 24, 8911–8926, https://doi.org/10.5194/acp-24-8911-2024, https://doi.org/10.5194/acp-24-8911-2024, 2024
Short summary
Short summary
Characterization of PM1 and positive matrix factorization (PMF) source apportionment of organic and inorganic fractions were conducted at the high-altitude station (HAC)2. Cloud presence reduced PM1, affecting sulfate more than organics. Free-troposphere (FT) conditions showed more black carbon (eBC) than planetary boundary layer (PBL) conditions.
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
Atmos. Chem. Phys., 24, 8737–8750, https://doi.org/10.5194/acp-24-8737-2024, https://doi.org/10.5194/acp-24-8737-2024, 2024
Short summary
Short summary
Environmental persistent free radicals (EPFRs) and reactive oxygen species (ROSs) play an active role in the atmosphere. Despite control measures having effectively reduced their emissions, reductions were less than in PM2.5. Emission control measures performed well in achieving Parade Blue, but reducing the impact of the atmosphere on human health remains challenging. Thus, there is a need to reassess emission control measures to better address the challenges posed by EPFRs and ROSs.
Fenghua Wei, Xing Peng, Liming Cao, Mengxue Tang, Ning Feng, Xiaofeng Huang, and Lingyan He
Atmos. Chem. Phys., 24, 8507–8518, https://doi.org/10.5194/acp-24-8507-2024, https://doi.org/10.5194/acp-24-8507-2024, 2024
Short summary
Short summary
The water solubility of secondary organic aerosols (SOAs) 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 SOAs 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.
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, Qingyan Fu, Douglas R. Worsnop, Jie Li, and Yele Sun
Atmos. Chem. Phys., 24, 8473–8488, https://doi.org/10.5194/acp-24-8473-2024, https://doi.org/10.5194/acp-24-8473-2024, 2024
Short summary
Short summary
We investigated aerosol composition and 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.
Feifei Li, Shanshan Tang, Jitao Lv, Shiyang Yu, Xu Sun, Dong Cao, Yawei Wang, and Guibin Jiang
Atmos. Chem. Phys., 24, 8397–8411, https://doi.org/10.5194/acp-24-8397-2024, https://doi.org/10.5194/acp-24-8397-2024, 2024
Short summary
Short summary
Targeted derivatization and non-targeted analysis with Fourier transform ion cyclotron resonance mass spectrometry (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 real samples.
Maya Abou-Ghanem, Daniel M. Murphy, Gregory P. Schill, Michael J. Lawler, and Karl D. Froyd
Atmos. Chem. Phys., 24, 8263–8275, https://doi.org/10.5194/acp-24-8263-2024, https://doi.org/10.5194/acp-24-8263-2024, 2024
Short summary
Short summary
Using particle analysis by laser mass spectrometry, we examine vanadium-containing ship exhaust particles measured on NASA's DC-8 during the Atmospheric Tomography Mission (ATom). Our results reveal ship exhaust particles are sufficiently widespread in the marine atmosphere and experience atmospheric aging. Finally, we use laboratory calibrations to determine the vanadium, sulfate, and organic single-particle mass fractions of vanadium-containing ship exhaust particles.
Cassandra J. Gaston, Joseph M. Prospero, Kristen Foley, Havala O. T. Pye, Lillian Custals, Edmund Blades, Peter Sealy, and James A. Christie
Atmos. Chem. Phys., 24, 8049–8066, https://doi.org/10.5194/acp-24-8049-2024, https://doi.org/10.5194/acp-24-8049-2024, 2024
Short summary
Short summary
To understand how changing emissions have impacted aerosols in remote regions, we measured nitrate and sulfate in Barbados and compared them 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 in sulfur dioxide (SO2) in the US and Europe; then it increased in the 2000s, likely due to anthropogenic emissions from Africa.
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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.
Xiao He, Xuan Zheng, Shuwen Guo, Lewei Zeng, Ting Chen, Bohan Yang, Shupei Xiao, Qiongqiong Wang, Zhiyuan Li, Yan You, Shaojun Zhang, and Ye Wu
EGUsphere, https://doi.org/10.5194/egusphere-2024-1671, https://doi.org/10.5194/egusphere-2024-1671, 2024
Short summary
Short summary
This study introduces an innovative method for identifying and quantifying complex organic vapors and aerosols. By combining advanced analytical techniques and new algorithms, we categorized thousands of compounds from heavy-duty diesel vehicles and ambient air and highlighted specific tracers for emission sources. The innovative approach enhances peak identification, reduces quantification uncertainties, and offers new insights for air quality management and atmospheric chemistry.
Xu Yang, Fobang Liu, Shuqi Yang, Yuling Yang, Yanan Wang, Jingjing Li, Mingyu Zhao, Zhao Wang, Kai Wang, Chi He, and Haijie Tong
EGUsphere, https://doi.org/10.5194/egusphere-2024-1622, https://doi.org/10.5194/egusphere-2024-1622, 2024
Short summary
Short summary
A study in rural North China Plain revealed Environmental persistent free radicals (EPFRs) in atmospheric particulate matter (PM), with a notable water-soluble fraction likely from atmospheric oxidation during transport. Significant positive correlations between EPFRs and the water-soluble oxidative potential of PM2.5 were found, primarily attributable to the water-soluble fractions of EPFRs. These findings emphasize understanding EPFRs’ atmospheric evolution for climate and health impacts.
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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.
Rime El Asmar, Zongrun Li, David J. Tanner, Yongtao Hu, Susan O’Neill, L. Gregory Huey, M. Talat Odman, and Rodney J. Weber
EGUsphere, https://doi.org/10.5194/egusphere-2024-1485, https://doi.org/10.5194/egusphere-2024-1485, 2024
Short summary
Short summary
Prescribed burning is an important method for managing ecosystems and preventing wildfires, however, smoke from prescribed fires can have a significant impact on air quality. Here, using a network of fixed sites and sampling throughout an extended prescribed burning period in two different years, we characterize the emissions and evolution up to 8 hours of PM2.5 mass, BC, and BrC in smoke from burning of forested lands in the southeastern US.
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
Short summary
Short summary
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.
Kirsten N. Fossum, Chunshui Lin, Niall O'Sullivan, Lu Lei, Stig Hellebust, Darius Ceburnis, Aqeel Afzal, Anja Tremper, David Green, Srishti Jain, Steigvilė Byčenkienė, Colin O'Dowd, John Wenger, and Jurgita Ovadnevaite
EGUsphere, https://doi.org/10.5194/egusphere-2024-1262, https://doi.org/10.5194/egusphere-2024-1262, 2024
Short summary
Short summary
The chemical composition and sources of submicron aerosol in the Dublin Port area were investigated over a month-long campaign. Two distinct types of ship emissions were identified and characterized: sulfate-rich plumes from use of heavy fuel oil with scrubbers and organic-rich plumes from use of low sulfur fuels. The latter were more frequent, emitting double the particle number, and having atypical V/Ni ratio for ship emission.
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
Short summary
Short summary
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
Short summary
Short summary
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.
Liyuan Zhou, Qianyun Liu, Christian M. Salvador, Michael Le Breton, Mattias Hallquist, Jian Zhen Yu, Chak K. Chan, and Åsa M. Hallquist
EGUsphere, https://doi.org/10.5194/egusphere-2024-494, https://doi.org/10.5194/egusphere-2024-494, 2024
Short summary
Short summary
Our research on city bus emissions reveals that alternative fuels (compressed natural gas and biofuels) reduce fresh particle emissions compared to diesel. However, all fuels lead to secondary air pollution. Aiming at guiding better environmental policies, we studied 76 buses using advanced emission measurement techniques. This work sheds light on the complex effects of bus fuels on urban air quality, emphasizing the need for comprehensive evaluations of future transportation technologies.
Meng Wang, Qiyuan Wang, Steven Sai Hang Ho, Jie Tian, Yong Zhang, Shun-cheng Lee, and Junji Cao
EGUsphere, https://doi.org/10.5194/egusphere-2024-1130, https://doi.org/10.5194/egusphere-2024-1130, 2024
Short summary
Short summary
This study explores nitrogen-containing organic compounds (NOCs) in PM2.5 particles on the Southeastern Tibetan Plateau. We discovered that biomass burning and transboundary transport are the primary sources of NOCs in the high-altitude area. Understanding these aerosol sources informs how they contribute to regional and potentially global climate changes. Our findings could help shape effective environmental policies to enhance air quality and address climate impacts in this sensitive region.
Yu Xu, Tang Liu, Yi-Jia Ma, Qi-Bin Sun, Hong-Wei Xiao, Hao Xiao, and Hua-Yun Xiao
EGUsphere, https://doi.org/10.5194/egusphere-2024-975, https://doi.org/10.5194/egusphere-2024-975, 2024
Short summary
Short summary
This study has explored the characteristics of aminiums, ammonium, and PM2.5 from the clean days to the polluted days according to the observational data from 11 different Chinese cities, highlighting the possibility of the competitive uptake of ammonia versus amines on acidic aerosols, or the displacement of aminiums by ammonia under a high ammonia condition. The overall results deepen the understanding of the spatiotemporal differences in aminium characteristic and formation in China.
Qun He, Zhaowen Wang, Houfeng Liu, Pengju Xu, Rongbao Duan, Caihong Xu, Jianmin Chen, and Min Wei
EGUsphere, https://doi.org/10.5194/egusphere-2024-841, https://doi.org/10.5194/egusphere-2024-841, 2024
Short summary
Short summary
Coastal environments provide an ideal setting for investigating the intermixing processes of terrestrial and marine aerosols. Terrestrial air mass constituted a larger proportion during severe air pollution, harboring more animal and human pathogens. A relative shift towards marine air-mass with respect to pollution elimination, where saprophytic bacteria and fungi were predominant. Mixed air-mass reveals the intermixing processes of terrestrial and marine sources.
Maria P. Velásquez-García, K. Santiago Hernández, James A. Vergara-Correa, Richard J. Pope, Miriam Gómez-Marín, and Angela M. Rendón
EGUsphere, https://doi.org/10.5194/egusphere-2024-695, https://doi.org/10.5194/egusphere-2024-695, 2024
Short summary
Short summary
For the Aburrá Valley, Colombia, local emissions dominate aerosol concentrations, which degrade air quality (AQ) and impact human health. However, this can be exacerbated by the influx of external emissions from sources such as regional fires, Saharan dust, and volcanic degassing. While substantially increasing city-wide aerosols, these external sources can also degrade the aerosol chemical composition (i.e. their toxicity) and impact AQ, which we investigate in this study.
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
Short summary
Short summary
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.
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
Short summary
Short summary
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.
Jinbo Wang, Jiaping Wang, Yuxuan Zhang, Tengyu Liu, Xuguang Chi, Xin Huang, Dafeng Ge, Shiyi Lai, Caijun Zhu, Lei Wang, Qiaozhi Zha, Ximeng Qi, Wei Nie, Congbin Fu, and Aijun Ding
EGUsphere, https://doi.org/10.5194/egusphere-2024-879, https://doi.org/10.5194/egusphere-2024-879, 2024
Short summary
Short summary
In this study, we found large spatial discrepancies in the physical and chemical properties of black carbon over the Tibetan Plateau (TP). Elevated anthropogenic emissions from low-altitude regions can significantly change the mass concentration, mixing state and chemical composition of black carbon -containing aerosol in TP region, further altering its light absorption ability. Our study emphasizes the vulnerability of remote plateau regions to intense anthropogenic influences.
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
Short summary
Short summary
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.
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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.
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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.
Cited articles
Allen, H. M., Draper, D. C., Ayres, B. R., Ault, A., Bondy, A., Takahama, S., Modini, R. L., Baumann, K., Edgerton, E., Knote, C., Laskin, A.,
Wang, B., and Fry, J. L.: Influence of crustal dust and sea spray supermicron particle concentrations and acidity on inorganic aerosol
during the 2013 Southern Oxidant and Aerosol Study, Atmos. Chem. Phys., 15, 10669–10685, https://doi.org/10.5194/acp-15-10669-2015, 2015.
Anttila, T., Kiendler-Scharr, A., Mentel, T. F., and Tillmann, R.: Size
dependent partitioning of organic material: evidence for the formation of
organic coatings on aqueous aerosols, J. Atmos. Chem., 57, 215–237, 2007.
Artaxo, P. and Orsini, C.: PIXE and receptor models applied to remote
aerosol source apportionment in Brazil, Nucl. Instrum. Methods,
Sect. B, 22, 259–263, 1987.
Attwood, A. R., Washenfelder, R. A., Brock, C. A., Hu, W., Baumann, K.,
Campuzano-Jost, P., Day, D. A., Edgerton, E. S., Murphy, D. M., Palm, B. B.,
McComiskey, A., Wagner, N. L., de Sá, S. S., Ortega, A., Martin, S. T.,
Jimenez, J. L., and Brown, S. S.: Trends in sulfate and organic aerosol mass
in the Southeast U.S.: Impact on aerosol optical depth and radiative
forcing, Geophys. Res. Lett., 41, 7701–7709, 2014.
Ault, A. P. and Axson, J. L.: Atmospheric Aerosol Chemistry: Spectroscopic
and Microscopic Advances, Anal. Chem., 89, 430–452, 2017.
Ault, A. P., Moore, M. J., Furutani, H., and Prather, K. A.: Impact of
emissions from the Los Angeles port region on San Diego air quality,
Environ. Sci. Technol., 43, 3500–3506, 2009.
Ault, A. P., Gaston, C. J., Wang, Y., Dominguez, G., Thiemens, M. H., and
Prather, K. A.: Characterization of the single particle mixing state of
individual ship plume events measured at the Port of Los Angeles, Environ.
Sci. Technol., 44, 1954–1961, 2010.
Ault, A. P., Peters, T. M., Sawvel, E. J., Casuccio, G. S., Willis, R. D.,
Norris, G. A., and Grassian, V. H.: Single-particle SEM-EDX analysis of
iron-containing coarse particulate matter in an urban environment: Sources
and distribution of iron within Cleveland, Ohio, Environ. Sci. Technol., 46,
4331–4339, 2012.
Ault, A. P., Moffet, R. C., Baltrusaitis, J., Collins, D. B., Ruppel, M. J.,
Cuadra-Rodriguez, L. A., Zhao, D., Guasco, T. L., Ebben, C. J., Geiger, F.
M., Bertram, T. H., Prather, K. A., and Grassian, V. H.: Size-dependent
changes in sea spray serosol composition and properties with different
seawater conditions, Environ. Sci. Technol., 47, 5603–5612, 2013a.
Ault, A. P., Zhao, D., Ebben, C. J., Tauber, M. J., Geiger, F. M., Prather,
K. A., and Grassian, V. H.: Raman microspectroscopy and vibrational sum
frequency generation spectroscopy as probes of the bulk and surface
compositions of size-resolved sea spray aerosol particles, Phys. Chem. Chem.
Phys., 15, 6206–6214, 2013b.
Axson, J. L., May, N. W., Colon-Bernal, I. D., Pratt, K. A., and Ault, A.
P.: Lake Spray Aerosol: A Chemical Signature from Individual Ambient
Particles, Environ. Sci. Technol., 50, 9835–9845, 2016a.
Axson, J. L., Shen, H. R., Bondy, A. L., Landry, C. C., Welz, J., Creamean,
J. M., and Ault, A. P.: Transported mineral dust deposition case study at a
hydrologically sensitive mountain site: Size and composition shifts in
ambient aerosol and snowpack, Aerosol Air Qual. Res., 16, 555–567, 2016b.
Ayres, B. R., Allen, H. M., Draper, D. C., Brown, S. S., Wild, R. J., Jimenez, J. L., Day, D. A., Campuzano-Jost, P., Hu, W., de Gouw, J., Koss, A.,
Cohen, R. C., Duffey, K. C., Romer, P., Baumann, K., Edgerton, E., Takahama, S., Thornton, J. A., Lee, B. H., Lopez-Hilfiker, F. D., Mohr, C.,
Wennberg, P. O., Nguyen, T. B., Teng, A., Goldstein, A. H., Olson, K., and Fry, J. L.: Organic nitrate aerosol formation via NO3 + biogenic volatile
organic compounds in the southeastern United States, Atmos. Chem. Phys., 15, 13377–13392, https://doi.org/10.5194/acp-15-13377-2015, 2015.
Bondy, A. L., Kirpes, R. M., Merzel, R. L., Pratt, K. A., Banaszak Holl, M.
M., and Ault, A. P.: Atomic Force Microscopy-Infrared Spectroscopy of
Individual Atmospheric Aerosol Particles: Subdiffraction Limit Vibrational
Spectroscopy and Morphological Analysis, Anal. Chem., 89, 8594–8598, 2017a.
Bondy, A. L., Wang, B., Laskin, A., Craig, R. L., Nhliziyo, M. V., Bertman,
S. B., Pratt, K. A., Shepson, P. B., and Ault, A. P.: Inland Sea Spray
Aerosol Transport and Incomplete Chloride Depletion: Varying Degrees of
Reactive Processing Observed during SOAS, Environ. Sci. Technol., 51,
9533–9542, 2017b.
Bondy, A. L., Craig, R. L., Zhang, Z., Gold, A., Surratt, J. D., and Ault,
A. P.: Isoprene-Derived Organosulfates: Vibrational Mode Analysis by Raman
Spectroscopy, Acidity-Dependent Spectral Modes, and Observation in
Individual Atmospheric Particles, J. Phys. Chem. A, 122, 303–315, 2018.
Boone, E. J., Laskin, A., Laskin, J., Wirth, C., Shepson, P. B., Stirm, B.
H., and Pratt, K. A.: Aqueous Processing of Atmospheric Organic Particles in
Cloud Water Collected via Aircraft Sampling, Environ. Sci. Technol., 49,
8523–8530, 2015.
Boyd, C. M., Sanchez, J., Xu, L., Eugene, A. J., Nah, T., Tuet, W. Y., Guzman, M. I., and Ng, N. L.: Secondary organic aerosol formation from the
β-pinene+NO3 system: effect of humidity and peroxy radical fate, Atmos. Chem. Phys., 15, 7497–7522, https://doi.org/10.5194/acp-15-7497-2015, 2015.
Budisulistiorini, S. H., Li, X., Bairai, S. T., Renfro, J., Liu, Y., Liu, Y. J., McKinney, K. A., Martin, S. T., McNeill, V. F., Pye, H. O. T.,
Nenes, A., Neff, M. E., Stone, E. A., Mueller, S., Knote, C., Shaw, S. L., Zhang, Z., Gold, A., and Surratt, J. D.: Examining the effects of
anthropogenic emissions on isoprene-derived secondary organic aerosol formation during the 2013 Southern Oxidant and Aerosol Study (SOAS) at
the Look Rock, Tennessee ground site, Atmos. Chem. Phys., 15, 8871–8888, https://doi.org/10.5194/acp-15-8871-2015, 2015a.
Buha, J., Mueller, N., Nowack, B., Ulrich, A., Losert, S., and Wang, J.:
Physical and chemical characterization of fly ashes from swiss waste
incineration plants and determination of the ash fraction in the nanometer
range, Environ. Sci. Technol., 48, 4765–4773, 2014.
Carlton, A. G., Pinder, R. W., Bhave, P. V., and Pouliot, G. A.: To what
extent can biogenic SOA be controlled?, Environ. Sci. Technol., 44,
3376–3380, 2010.
Carlton, A. G., Wiedinmyer, C., and Kroll, J. H.: A review of Secondary Organic Aerosol (SOA) formation from isoprene,
Atmos. Chem. Phys., 9, 4987–5005, https://doi.org/10.5194/acp-9-4987-2009, 2009.
Carlton, A. G., Gouw, J. D., Jimenez, J. L., Ambrose, J. L., Attwood, A. R.,
Brown, S., Baker, K. R., Brock, C., Cohen, R. C., Edgerton, S., Farkas, C.
M., Farmer, D., Goldstein, A. H., Gratz, L., Guenther, A., Hunt, S.,
Jaeglé, L., Jaffe, D. A., Mak, J., McClure, C., Nenes, A., Nguyen, T.
K., Pierce, J. R., Sa, S. D., Selin, N. E., Shah, V., Shaw, S., Shepson, P.
B., Song, S., Stutz, J., Surratt, J. D., Turpin, B. J., Warneke, C.,
Washenfelder, R. A., Wennberg, P. O., and Zhou, X.: Synthesis of the
Southeast Atmosphere Studies: Investigating Fundamental Atmospheric
Chemistry Questions, B. Am. Meteorol. Soc., 99,
547–567, 2018.
Cerully, K. M., Bougiatioti, A., Hite Jr., J. R., Guo, H., Xu, L., Ng, N. L., Weber, R., and Nenes, A.: On the link between hygroscopicity,
volatility, and oxidation state of ambient and water-soluble aerosols in the southeastern United States, Atmos. Chem. Phys., 15, 8679–8694,
https://doi.org/10.5194/acp-15-8679-2015, 2015.
Chameides, W. L., Lindsay, R. W., Richardson, J., and Kiang, C. S.: The role
of biogenic hydrocarbons in urban photochemical smog: Atlanta as a case
study, Science, 241, 1473–1475, 1988.
Chang, R. Y.-W., Slowik, J. G., Shantz, N. C., Vlasenko, A., Liggio, J., Sjostedt, S. J., Leaitch, W. R., and Abbatt, J. P. D.: The
hygroscopicity parameter (κ) of ambient organic aerosol at a field site subject to biogenic and anthropogenic influences:
relationship to degree of aerosol oxidation, Atmos. Chem. Phys., 10, 5047–5064, https://doi.org/10.5194/acp-10-5047-2010, 2010.
Chen, H., Laskin, A., Baltrusaitis, J., Gorski, C. A., Scherer, M. M., and
Grassian, V. H.: Coal Fly Ash as a Source of Iron in Atmospheric Dust,
Environ. Sci. Technol., 46, 2112–2120, 2012.
Chen, J., Li, C., Ristovski, Z., Milic, A., Gu, Y., Islam, M. S., Wang, S.,
Hao, J., Zhang, H., He, C., Guo, H., Fu, H., Miljevic, B., Morawska, L.,
Thai, P., Lam, Y. F., Pereira, G., Ding, A., Huang, X., and Dumka, U. C.: A
review of biomass burning: emissions and impacts on air quality, health and
climate in China, Sci. Total Environ., 579, 1000–1034, 2017.
Chi, J. W., Li, W. J., Zhang, D. Z., Zhang, J. C., Lin, Y. T., Shen, X. J., Sun, J. Y., Chen, J. M., Zhang, X. Y., Zhang, Y. M., and
Wang, W. X.: Sea salt aerosols as a reactive surface for inorganic and organic acidic gases in the Arctic troposphere, Atmos. Chem. Phys., 15,
11341–11353, https://doi.org/10.5194/acp-15-11341-2015, 2015.
Chung, S. H. and Seinfeld, J. H.: Climate response of direct radiative
forcing of anthropogenic black carbon, J. Geophys. Res.-Atmos., 110, D11102,
https://doi.org/10.1029/2004JD005441, 2005.
Cong, Z., Kang, S., Dong, S., Liu, X., and Qin, D.: Elemental and individual
particle analysis of atmospheric aerosols from high Himalayas, Environ.
Monit. Assess., 160, 323–335, 2010.
Conny, J. M. and Norris, G. A.: Scanning Electron Microanalysis and
Analytical Challenges of Mapping Elements in Urban Atmospheric Particles,
Environ. Sci. Technol., 45, 7380–7386, 2011.
Coz, E., Gómez-Moreno, F. J., Pujadas, M., Casuccio, G. S., Lersch, T.
L., and Artíñano, B.: Individual particle characteristics of North
African dust under different long-range transport scenarios, Atmos.
Environ., 43, 1850–1863, 2009.
Craig, R. L. and Ault, A. P.: Aerosol Acidity: Direct Measurement from a
Spectroscopic Method, in: Multiphase Environmental Chemistry in the
Atmosphere, edited by: Hunt, S. W., Laskin, A., and Nizkorodov, S., ACS Books
Special Symposium Series, 2018.
Craig, R. L., Bondy, A. L., and Ault, A. P.: Computer-controlled Raman
microspectroscopy (CC-Raman): A method for the rapid characterization of
individual atmospheric aerosol particles, Aerosol Sci. Technol., 51,
1099–1112, 2017.
Creamean, J. M., Axson, J. L., Bondy, A. L., Craig, R. L., May, N. W., Shen,
H., Weber, M. H., Pratt, K. A., and Ault, A. P.: Changes in precipitating
snow chemistry with location and elevation in the California Sierra Nevada,
J. Geophys. Res.-Atmos., 121, 7296–7309, 2016.
Deboudt, K., Gloter, A., Mussi, A., and Flament, P.: Red-ox speciation and
mixing state of iron in individual African dust particles, J. Geophys.
Res.-Atmos., 117, D12307, https://doi.org/10.1029/2011JD017298, 2012.
Dickau, M., Olfert, J., Stettler, M. E. J., Boies, A., Momenimovahed, A.,
Thomson, K., Smallwood, G., and Johnson, M.: Methodology for quantifying the
volatile mixing state of an aerosol, Aerosol Sci. Technol., 50, 759–772,
2016.
Ebben, C. J., Ault, A. P., Ruppel, M. J., Ryder, O. S., Bertram, T. H.,
Grassian, V. H., Prather, K. A., and Geiger, F. M.: Size-Resolved Sea Spray
Aerosol Particles Studied by Vibrational Sum Frequency Generation, J. Phys.
Chem. A, 117, 6589–6601, 2013.
Estillore, A. D., Trueblood, J. V., and Grassian, V. H.: Atmospheric
chemistry of bioaerosols: heterogeneous and multiphase reactions with
atmospheric oxidants and other trace gases, Chem. Sci., 7, 6604–6616,
2016.
Fang, T., Guo, H. Y., Zeng, L. H., Verma, V., Nenes, A., and Weber, R. J.:
Highly Acidic Ambient Particles, Soluble Metals, and Oxidative Potential: A
Link between Sulfate and Aerosol Toxicity, Environ. Sci. Technol., 51,
2611–2620, 2017.
Fitzgerald, E., Ault, A. P., Zauscher, M. D., Mayol-Bracero, O. L., and
Prather, K. A.: Comparison of the mixing state of long-range transported
Asian and African mineral dust, Atmos. Environ., 115, 19–25, 2015.
Fraund, M., Pham, D., Bonanno, D., Harder, T., Wang, B., Brito, J., de
Sá, S., Carbone, S., China, S., Artaxo, P., Martin, S., Pöhlker, C.,
Andreae, M., Laskin, A., Gilles, M., and Moffet, R.: Elemental mixing state
of aerosol particles collected in Central Amazonia during GoAmazon2014/15,
Atmosphere, 8, 173, https://doi.org/10.3390/atmos8090173, 2017.
Froyd, K. D., Murphy, S. M., Murphy, D. M., de Gouw, J. A., Eddingsaas, N.
C., Wennberg, P. O., and Thiemens, M. H.: Contribution of isoprene-derived
organosulfates to free tropospheric aerosol mass, P. Natl. Acad. Sci. USA, 107, 21360–21365, 2010.
Fu, H., Zhang, M., Li, W., Chen, J., Wang, L., Quan, X., and Wang, W.: Morphology, composition and mixing state of individual carbonaceous aerosol
in urban Shanghai, Atmos. Chem. Phys., 12, 693–707, https://doi.org/10.5194/acp-12-693-2012, 2012.
Gantt, B. and Meskhidze, N.: The physical and chemical characteristics of marine primary organic aerosol: a review, Atmos. Chem. Phys.,
13, 3979–3996, https://doi.org/10.5194/acp-13-3979-2013, 2013.
Ghorai, S., Wang, B., Tivanski, A., and Laskin, A.: Hygroscopic properties
of internally mixed particles composed of NaCl and water-soluble organic
acids, Environ. Sci. Technol., 48, 2234–2241, 2014.
Giordano, M., Espinoza, C., and Asa-Awuku, A.: Experimentally measured morphology of biomass burning aerosol and its impacts on CCN
ability, Atmos. Chem. Phys., 15, 1807–1821, https://doi.org/10.5194/acp-15-1807-2015, 2015.
Giorio, C., Tapparo, A., Dall'Osto, M., Beddows, D. C. S., Esser-Gietl, J.
K., Healy, R. M., and Harrison, R. M.: Local and regional components of
aerosol in a heavily trafficked street canyon in central London derived from
PMF and cluster analysis of single-particle ATOFMS spectra, Environ. Sci.
Technol., 49, 3330–3340, 2015.
Goldstein, A. H., Koven, C. D., Heald, C. L., and Fung, I. Y.: Biogenic
carbon and anthropogenic pollutants combine to form a cooling haze over the
southeastern United States, P. Natl. Acad. Sci. USA, 106, 8835–8840,
2009.
Guo, H., Xu, L., Bougiatioti, A., Cerully, K. M., Capps, S. L., Hite Jr., J. R., Carlton, A. G., Lee, S.-H., Bergin, M. H., Ng, N. L.,
Nenes, A., and Weber, R. J.: Fine-particle water and pH in the southeastern
United States, Atmos. Chem. Phys., 15, 5211–5228, https://doi.org/10.5194/acp-15-5211-2015, 2015.
Guo, H., Nenes, A., and Weber, R. J.: The underappreciated role of nonvolatile cations on aerosol ammonium-sulfate molar ratios, Atmos. Chem. Phys. Discuss.,
https://doi.org/10.5194/acp-2017-737, in review, 2017.
Hashemi, S. S., Baghernejad, M., and Khademi, H.: Micromorphology of gypsum
crystals in southern Iranian soils under different moisture regimes, J.
Agric. Sci. Technol., 13, 273–288, 2011.
Hatch, L. E., Creamean, J. M., Ault, A. P., Surratt, J. D., Chan, M. N.,
Seinfeld, J. H., Edgerton, E. S., Su, Y., and Prather, K. A.: Measurements
of Isoprene-Derived Organosulfates in Ambient Aerosols by Aerosol
Time-of-Flight Mass Spectrometry – Part 1: Single Particle Atmospheric
Observations in Atlanta, Environ. Sci. Technol., 45, 5105–5111, 2011.
Healy, R. M., Evans, G. J., Murphy, M., Juranyi, Z., Tritscher, T., Laborde,
M., Weingartner, E., Gysel, M., Poulain, L., Kamilli, K. A., Wiedensohler,
A., O'Connor, I. P., McGillicuddy, E., Sodeau, J. R., and Wenger, J. C.:
Predicting hygroscopic growth using single particle chemical composition
estimates, J. Geophys. Res.-Atmos., 119, 9567–9577, 2014a.
Healy, R. M., Riemer, N., Wenger, J. C., Murphy, M., West, M., Poulain, L., Wiedensohler, A., O'Connor, I. P.,
McGillicuddy, E., Sodeau, J. R., and Evans, G. J.: Single particle diversity and mixing state
measurements, Atmos. Chem. Phys., 14, 6289–6299, https://doi.org/10.5194/acp-14-6289-2014, 2014b.
Healy, R. M., Wang, J. M., Jeong, C. H., Lee, A. K. Y., Willis, M. D.,
Jaroudi, E., Zimmerman, N., Hilker, N., Murphy, M., Eckhardt, S., Stohl, A.,
Abbatt, J. P. D., Wenger, J. C., and Evans, G. J.: Light-absorbing
properties of ambient black carbon and brown carbon from fossil fuel and
biomass burning sources, J. Geophys. Res.-Atmos., 120, 6619–6633, 2015.
Hidy, G. M., Blanchard, C. L., Baumann, K., Edgerton, E., Tanenbaum, S., Shaw, S., Knipping, E., Tombach, I., Jansen, J., and Walters, J.:
Chemical climatology of the southeastern United States, 1999–2013, Atmos. Chem. Phys., 14, 11893–11914, https://doi.org/10.5194/acp-14-11893-2014, 2014.
Hinds, W. C.: Aerosol Technology Properties, Behavior, and Measurement of
Airborne Particles, John Wiley & Sons, Inc., New York, 1999.
Hiranuma, N., Brooks, S. D., Moffet, R. C., Glen, A., Laskin, A., Gilles, M.
K., Liu, P., Macdonald, A. M., Strapp, J. W., and McFarquhar, G. M.:
Chemical characterization of individual particles and residuals of cloud
droplets and ice crystals collected on board research aircraft in the ISDAC
2008 study, J. Geophys. Res.-Atmos., 118, 6564–6579, 2013.
Hodas, N., Sullivan, A. P., Skog, K., Keutsch, F. N., Collett, J. L.,
Decesari, S., Facchini, M. C., Carlton, A. G., Laaksonen, A., and Turpin, B.
J.: Aerosol liquid water driven by anthropogenic nitrate: implications for
lifetimes of water-soluble organic gases and potential for secondary organic
aerosol formation, Environ. Sci. Technol., 48, 11127–11136, 2014.
Hopkins, R. J., Desyaterik, Y., Tivanski, A. V., Zaveri, R. A., Berkowitz, C.
M., Tyliszczak, T., Gilles, M. K., and Laskin, A.: Chemical speciation of
sulfur in marine cloud droplets and particles: Analysis of individual
particles from the marine boundary layer over the California current, J.
Geophys. Res.-Atmos., 113, D04209, https://doi.org/10.1029/2007JD008954, 2008.
Hu, W. W., Campuzano-Jost, P., Palm, B. B., Day, D. A., Ortega, A. M., Hayes, P. L., Krechmer, J. E., Chen, Q., Kuwata, M., Liu, Y. J., de Sá, S. S.,
McKinney, K., Martin, S. T., Hu, M., Budisulistiorini, S. H., Riva, M., Surratt, J. D., St. Clair, J. M., Isaacman-Van Wertz, G., Yee, L. D.,
Goldstein, A. H., Carbone, S., Brito, J., Artaxo, P., de Gouw, J. A., Koss, A., Wisthaler, A., Mikoviny, T., Karl, T., Kaser, L., Jud, W.,
Hansel, A., Docherty, K. S., Alexander, M. L., Robinson, N. H., Coe, H., Allan, J. D., Canagaratna, M. R., Paulot, F., and Jimenez, J. L.:
Characterization of a real-time tracer for isoprene epoxydiols-derived secondary organic aerosol (IEPOX-SOA) from aerosol mass spectrometer
measurements, Atmos. Chem. Phys., 15, 11807–11833, https://doi.org/10.5194/acp-15-11807-2015, 2015.
Huffman, J. A., Sinha, B., Garland, R. M., Snee-Pollmann, A., Gunthe, S. S., Artaxo, P., Martin, S. T., Andreae, M. O., and Pöschl, U.: Size
distributions and temporal variations of biological aerosol particles in the Amazon rainforest characterized by microscopy and real-time
UV-APS fluorescence techniques during AMAZE-08, Atmos. Chem. Phys., 12, 11997–12019, https://doi.org/10.5194/acp-12-11997-2012, 2012.
Jacobson, M. Z. Z.: Strong radiative heating due to the mixing state of
black carbon in atmospheric aerosols, Nature, 409, 695–697, 2001.
Kandler, K., Lieke, K., Benker, N., Emmel, C., Küpper, M.,
Müller-Ebert, D., Ebert, M., Scheuvens, D., Schladitz, A., Schütz,
L., and Weinbruch, S.: Electron microscopy of particles collected at Praia,
Cape Verde, during the Saharan Mineral Dust Experiment: particle chemistry,
shape, mixing state and complex refractive index, Tellus B, 63, 475–496,
https://doi.org/10.1111/j.1600-0889.2011.00550.x, 2011.
Kilcoyne, A. L. D., Tyliszczak, T., Steele, W. F., Fakra, S., Hitchcock, P.,
Franck, K., Anderson, E., Harteneck, B., Rightor, E. G., Mitchell, G. E.,
Hitchcock, A. P., Yang, L., Warwick, T., and Ade, H.:
Interferometer-controlled scanning transmission X-ray microscopes at the
Advanced Light Source, J. Synchrotron Radiat., 10, 125–136, 2003.
Kim, J.-S. and Park, K.: Atmospheric aging of Asian dust particles during
long range transport, Aerosol Sci. Technol., 46, 913–924, 2012.
Kirpes, R. M., Bondy, A. L., Bonanno, D., Moffet, R. C., Wang, B., Laskin, A., Ault, A. P., and Pratt, K. A.: Secondary sulfate is internally mixed
with sea spray aerosol and organic aerosol in the winter Arctic, Atmos. Chem. Phys., 18, 3937–3949, https://doi.org/10.5194/acp-18-3937-2018, 2018.
Kunkel, D., Lawrence, M. G., Tost, H., Kerkweg, A., Jockel, P., and Borrmann,
S.: Urban emission hot spots as sources for remote aerosol deposition,
Geophys. Res. Lett., 39, L01808, https://doi.org/10.1029/2011GL049634, 2012.
Laskin, A., Iedema, M. J., and Cowin, J. P.: Quantitative time-resolved
monitoring of nitrate formation in sea salt particles using a CCSEM/EDX
single particle analysis, Environ. Sci. Technol., 36, 4948–4955, 2002.
Laskin, A., Iedema, M. J., Ichkovich, A., Graber, E. R., Taraniuk, I., and
Rudich, Y.: Direct observation of completely processed calcium carbonate
dust particles, Faraday Discuss., 130, 453–468, 2005.
Laskin, A., Cowin, J. P., and Iedema, M. J.: Analysis of individual
environmental particles using modern methods of electron microscopy and
X-ray microanalysis, J. Electron Spectrosc., 150, 260–274,
2006.
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, D15302,
https://doi.org/10.1029/2012JD017743, 2012.
Lee, S., Wang, Y. H., and Russell, A. G.: Assessment of secondary organic
carbon in the southeastern United States: A review, J. Air
Waste Manage. Assoc., 60, 1282–1292, 2010.
Li, C., Hu, Y., Chen, J., Ma, Z., Ye, X., Yang, X., Wang, L., Wang, X., and
Mellouki, A.: Physiochemical properties of carbonaceous aerosol from
agricultural residue burning: Density, volatility, and hygroscopicity,
Atmos. Environ., 140, 94–105, 2016.
Li, J., Posfai, M., Hobbs, P. V., and Buseck, P. R.: Individual aerosol
particles from biomass burning in southern Africa: 2, Compositions and aging
of inorganic particles, J. Geophys. Res.-Atmos., 108, 8484,
https://doi.org/10.1029/2002JD002310, 2003.
Li, W., Shao, L., Zhang, D., Ro, C.-U., Hu, M., Bi, X., Geng, H., Matsuki,
A., Niu, H., and Chen, J.: A review of single aerosol particle studies in
the atmosphere of East Asia: Morphology, mixing state, source, and
heterogeneous reactions, J. Clean. Prod., 112, 1330–1349, 2016.
Li, W., Xu, L., Liu, X., Zhang, J., Lin, Y., Yao, X., Gao, H., Zhang, D.,
Chen, J., Wang, W., Harrison, R. M., Zhang, X., Shao, L., Fu, P., Nenes, A.,
and Shi, Z.: Air pollution–aerosol interactions produce more bioavailable
iron for ocean ecosystems, Sci. Adv., 3, e1601749,
https://doi.org/10.1126/sciadv.1601749, 2017.
Lu, J. W., Flores, J. M., Lavi, A., Abo-Riziq, A., and Rudich, Y.: Changes
in the optical properties of benzo[a]pyrene-coated aerosols upon
heterogeneous reactions with NO2 and NO3, PCCP, 13, 6484–6492,
2011.
Manninen, H. E., Back, J., Sihto-Nissila, S. L., Huffman, J. A., Pessi, A.
M., Hiltunen, V., Aalto, P. P., Hidalgo, P. J., Hari, P., Saarto, A.,
Kulmala, M., and Petaja, T.: Patterns in airborne pollen and other primary
biological aerosol particles (PBAP), and their contribution to aerosol mass
and number in a boreal forest, Boreal Environ. Res., 19, 383–405,
2014.
Marple, V. A., Rubow, K. L., and Behm, S. M.: A microorifice uniform deposit
impactor (MOUDI)-description, calibration and use, Aerosol Sci. Technol.,
14, 434–446, 1991.
May, N. W., Axson, J. L., Watson, A., Pratt, K. A., and Ault, A. P.: Lake spray aerosol generation: a method for producing
representative particles from freshwater wave breaking, Atmos. Meas. Tech., 9, 4311–4325, https://doi.org/10.5194/amt-9-4311-2016, 2016.
May, N. W., Gunsch, M. J., Olson, N. E., Bondy, A. L., Kirpes, R. M.,
Bertman, S. B., China, S., Laskin, A., Hopke, P. K., Ault, A. P., and Pratt,
K. A.: Unexpected Contributions of Sea Spray and Lake Spray Aerosol to
Inland Particulate Matter, Environ. Sci. Tech. Let., 5, 405–412, 2018a.
May, N. W., Olson, N. E., Panas, M., Axson, J. L., Tirella, P. S., Kirpes,
R. M., Craig, R. L., Gunsch, M. J., China, S., Laskin, A., Ault, A. P., and
Pratt, K. A.: Aerosol Emissions from Great Lakes Harmful Algal Blooms,
Environ. Sci. Technol., 52, 397–405, 2018b.
Metternich, P., Georgii, H. W., and Groeneveld, K. O.: Application of
particle induced X-ray emission to aerosol long-range transport
studies – transport pathways of pollution aerosol over the Atlantic ocean
and Europe, Atmos. Res., 20, 3–9, 1986.
Moffet, R. C., Prather, K. A., and Thiemens, M. H.: In-situ measurements of
the mixing state and optical properties of soot with implications for
radiative forcing estimates, P. Natl. Acad. Sci. USA, 106,
11872–11877, 2009.
Moffet, R. C., Henn, T., Laskin, A., and Gilles, M. K.: Automated chemical
analysis of internally mixed aerosol particles using X-ray spectromicroscopy
at the carbon K-edge, Anal. Chem., 82, 7906–7914, 2010a.
Moffet, R. C., Henn, T. R., Tivanski, A. V., Hopkins, R. J., Desyaterik, Y., Kilcoyne, A. L. D., Tyliszczak, T., Fast, J.,
Barnard, J., Shutthanandan, V., Cliff, S. S., Perry, K. D., Laskin, A., and Gilles, M. K.: Microscopic characterization of carbonaceous
aerosol particle aging in the outflow
from Mexico City, Atmos. Chem. Phys., 10, 961–976, https://doi.org/10.5194/acp-10-961-2010, 2010b.
Moffet, R. C., Rödel, T. C., Kelly, S. T., Yu, X. Y., Carroll, G. T., Fast, J., Zaveri, R. A., Laskin, A., and Gilles, M. K.:
Spectro-microscopic measurements of carbonaceous aerosol aging in Central California, Atmos. Chem. Phys., 13, 10445–10459,
https://doi.org/10.5194/acp-13-10445-2013, 2013.
Moffet, R. C., O'Brien, R. E., Alpert, P. A., Kelly, S. T., Pham, D. Q., Gilles, M. K., Knopf, D. A., and Laskin, A.: Morphology
and mixing of black carbon particles collected in central California during the CARES field study, Atmos. Chem. Phys., 16,
14515–14525, https://doi.org/10.5194/acp-16-14515-2016, 2016.
Moise, T., Flores, J. M., and Rudich, Y.: Optical Properties of Secondary
Organic Aerosols and Their Changes by Chemical Processes, Chem. Rev., 115,
4400–4439, 2015.
Nakao, S., Tang, P., Tang, X., Clark, C. H., Qi, L., Seo, E., Asa-Awuku, A.,
and Cocker Iii, D.: Density and elemental ratios of secondary organic
aerosol: Application of a density prediction method, Atmos. Environ., 68,
273–277, 2013.
Nguyen, T. K. V., Petters, M. D., Suda, S. R., Guo, H., Weber, R. J., and Carlton, A. G.: Trends in particle-phase liquid water
during the Southern Oxidant and Aerosol Study, Atmos. Chem. Phys., 14, 10911–10930, https://doi.org/10.5194/acp-14-10911-2014, 2014.
Nguyen, T. K. V., Capps, S. L., and Carlton, A. G.: Decreasing aerosol water
is consistent with OC trends in the southeast U.S, Environ. Sci. Technol.,
49, 7843–7850, 2015.
O'Brien, R. E., Wang, B. B., Laskin, A., Riemer, N., West, M., Zhang, Q.,
Sun, Y. L., Yu, X. Y., Alpert, P., Knopf, D. A., Gilles, M. K., and Moffet,
R. C.: Chemical imaging of ambient aerosol particles: Observational
constraints on mixing state parameterization, J. Geophys. Res.-Atmos., 120,
9591–9605, 2015.
Perlwitz, J. P., Pérez García-Pando, C., and Miller, R. L.: Predicting the mineral composition of dust aerosols – Part 1: Representing
key processes, Atmos. Chem. Phys., 15, 11593–11627, https://doi.org/10.5194/acp-15-11593-2015, 2015.
Pilson, M. E. Q.: An introduction to the chemistry of the sea, Prentice
Hall, 1998.
Portmann, R. W., Solomon, S., Hegerl, G. C., and Held, I. M.: Spatial and
seasonal patterns in climate change, temperatures, and precipitation across
the United States, P. Natl. Acad. Sci. USA, 106, 7324–7329, 2009.
Posfai, M. and Buseck, P. R.: Nature and climate dffects of individual
tropospheric aerosol particles, in: Annual Review of Earth and Planetary
Sciences, Vol. 38, edited by: Jeanloz, R. and Freeman, K. H., Annual Review of
Earth and Planetary Sciences, 2010.
Posfai, M., Simonics, R., Li, J., Hobbs, P. V., and Buseck, P. R.: Individual
aerosol particles from biomass burning in southern Africa: 1. Compositions
and size distributions of carbonaceous particles, J. Geophys. Res.-Atmos.,
108, 8483, https://doi.org/10.1029/2002JD002291, 2003.
Prather, K. A., Bertram, T. H., Grassian, V. H., Deane, G. B., Stokes, M.
D., DeMott, P. J., Aluwihare, L. I., Palenik, B. P., Azam, F., Seinfeld, J.
H., Moffet, R. C., Molina, M. J., Cappa, C. D., Geiger, F. M., Roberts, G.
C., Russell, L. M., Ault, A. P., Baltrusaitis, J., Collins, D. B., Corrigan,
C. E., Cuadra-Rodriguez, L. A., Ebben, C. J., Forestieri, S. D., Guasco, T.
L., Hersey, S. P., Kim, M. J., Lambert, W. F., Modini, R. L., Mui, W.,
Pedler, B. E., Ruppel, M. J., Ryder, O. S., Schoepp, N. G., Sullivan, R. C.,
and Zhao, D.: Bringing the ocean into the laboratory to probe the chemical
complexity of sea spray aerosol, P. Natl. Acad. Sci. USA, 110,
7550–7555, 2013.
Pratt, K. A. and Prather, K. A.: Aircraft measurements of vertical profiles
of aerosol mixing states, J. Geophys. Res.-Atmos., 115, D11305,
https://doi.org/10.1029/2009JD013150, 2010.
Pye, H. O. T., Luecken, D. J., Xu, L., Boyd, C. M., Ng, N. L., Baker, K. R.,
Ayres, B. R., Bash, J. O., Baumann, K., Carter, W. P. L., Edgerton, E., Fry,
J. L., Hutzell, W. T., Schwede, D. B., and Shepson, P. B.: Modeling the
current and future roles of particulate organic nitrates in the southeastern
United States, Environ. Sci. Technol., 49, 14195–14203, 2015.
Ramanathan, V. and Carmichael, G.: Global and regional climate changes due
to black carbon, Nat. Geosci., 1, 221–227, 2008.
Rattanavaraha, W., Chu, K., Budisulistiorini, S. H., Riva, M., Lin, Y.-H., Edgerton, E. S., Baumann, K., Shaw, S. L., Guo, H., King, L., Weber, R. J.,
Neff, M. E., Stone, E. A., Offenberg, J. H., Zhang, Z., Gold, A., and Surratt, J. D.: Assessing the impact of anthropogenic pollution on
isoprene-derived secondary organic aerosol formation in PM2.5 collected from the Birmingham, Alabama, ground site during the 2013
Southern Oxidant and Aerosol Study, Atmos. Chem. Phys., 16, 4897–4914, https://doi.org/10.5194/acp-16-4897-2016, 2016.
Riemer, N. and West, M.: Quantifying aerosol mixing state with entropy and diversity measures,
Atmos. Chem. Phys., 13, 11423–11439, https://doi.org/10.5194/acp-13-11423-2013,
2013.
Riva, M., Budisulistiorini, S. H., Zhang, Z., Gold, A., and Surratt, J. D.:
Chemical characterization of secondary organic aerosol constituents from
isoprene ozonolysis in the presence of acidic aerosol, Atmos. Environ., 130,
5–13, 2016.
Robinson, C. B., Schill, G. P., Zarzana, K. J., and Tolbert, M. A.: Impact
of organic coating on optical growth of ammonium sulfate particles, Environ.
Sci. Technol., 47, 13339–13346, 2013.
Saxena, V. K. and Yu, S. C.: Searching for a regional fingerprint of aerosol
radiative forcing in the southeastern US, Geophys. Res. Lett., 25,
2833–2836, 1998.
Schutgens, N. A. J. and Stier, P.: A pathway analysis of global aerosol processes, Atmos. Chem. Phys., 14,
11657–11686, https://doi.org/10.5194/acp-14-11657-2014, 2014.
Sedlacek III, A. J., Lewis, E. R., Kleinman, L., Xu, J., and Zhang, Q.:
Determination of and evidence for non-core-shell structure of particles
containing black carbon using the Single-Particle Soot Photometer (SP2),
Geophys. Res. Lett., 39, L06802, https://doi.org/10.1029/2012GL050905, 2012.
Shen, H., Peters, T. M., Casuccio, G. S., Lersch, T. L., West, R. R., Kumar,
A., Kumar, N., and Ault, A. P.: Elevated Concentrations of Lead in
Particulate Matter on the Neighborhood-Scale in Delhi, India As Determined
by Single Particle Analysis, Environ. Sci. Technol., 50, 4961–4970, 2016.
Sobanska, S., Coeur, C., Maenhaut, W., and Adams, F.: SEM-EDX
characterisation of tropospheric aerosols in the Negev desert (Israel), J.
Atmos. Chem., 44, 299–322, 2003.
Sobanska, S., Hwang, H., Choel, M., Jung, H.-J., Eom, H.-J., Kim, H.,
Barbillat, J., and Ro, C.-U.: Investigation of the chemical mixing state of
individual Asian dust particles by the combined use of electron probe X-ray
microanalysis and Raman microspectrometry, Anal. Chem., 84, 3145–3154, 2012.
Song, C. H., Kim, C. M., Lee, Y. J., Carmichael, G. R., Lee, B. K., and Lee,
D. S.: An evaluation of reaction probabilities of sulfate and nitrate
precursors onto East Asian dust particles, J. Geophys. Res.-Atmos., 112,
D18206, https://doi.org/10.1029/2006JD008092, 2007.
Sullivan, R. C., Guazzotti, S. A., Sodeman, D. A., and Prather, K. A.: Direct observations of the atmospheric processing of
Asian mineral dust, Atmos. Chem. Phys., 7, 1213–1236, https://doi.org/10.5194/acp-7-1213-2007, 2007.
Sullivan, R. C., Moore, M. J. K., Petters, M. D., Kreidenweis, S. M., Roberts, G. C., and Prather, K. A.: Effect of chemical mixing
state on the hygroscopicity and cloud nucleation properties of calcium mineral dust particles, Atmos. Chem. Phys., 9, 3303–3316, https://doi.org/10.5194/acp-9-3303-2009, 2009.
Tang, M. J., Cziczo, D. J., and Grassian, V. H.: Interactions of Water with
Mineral Dust Aerosol: Water Adsorption, Hygroscopicity, Cloud Condensation,
and Ice Nucleation, Chem. Rev., 116, 4205–4259, 2016.
Violaki, K. and Mihalopoulos, N.: Water-soluble organic nitrogen (WSON) in
size-segregated atmospheric particles over the Eastern Mediterranean, Atmos.
Environ., 44, 4339–4345, 2010.
Wagner, F., Bortoli, D., Pereira, S., Costa, M. J., Silva, A. M., Weinzierl,
B., Esselborn, M., Petzold, A., Rasp, K., Heinold, B., and Tegen, I. N. A.:
Properties of dust aerosol particles transported to Portugal from the Sahara
desert, Tellus B, 61, 297–306, 2009.
Washenfelder, R. A., Attwood, A. R., Brock, C. A., Guo, H., Xu, L., Weber, R.
J., Ng, N. L., Allen, H. M., Ayres, B. R., Baumann, K., Cohen, R. C., Draper,
D. C., Duffey, K. C., Edgerton, E., Fry, J. L., Hu, W. W., Jimenez, J. L.,
Palm, B. B., Romer, P., Stone, E. A., Wooldridge, P. J., and Brown, S. S.:
Biomass burning dominates brown carbon absorption in the rural southeastern
United States, Geophys. Res. Lett., 42, 2014GL062444,
https://doi.org/10.1002/2014GL062444, 2015.
Weber, R. J., Sullivan, A. P., Peltier, R. E., Russell, A., Yan, B., Zheng,
M., de Gouw, J., Warneke, C., Brock, C., Holloway, J. S., Atlas, E. L., and
Edgerton, E.: A study of secondary organic aerosol formation in the
anthropogenic-influenced southeastern United States, J. Geophys. Res.-Atmos.,
112, D13302, https://doi.org/10.1029/2007JD008408, 2007.
Weingartner, E., Burtscher, H., and Baltensperger, U.: Hygroscopic
properties of carbon and diesel soot particles, Atmos. Environ., 31,
2311–2327, 1997.
Xiong, F., McAvey, K. M., Pratt, K. A., Groff, C. J., Hostetler, M. A., Lipton, M. A., Starn, T. K., Seeley, J. V., Bertman, S. B., Teng, A. P.,
Crounse, J. D., Nguyen, T. B., Wennberg, P. O., Misztal, P. K., Goldstein, A. H., Guenther, A. B., Koss, A. R., Olson, K. F., de Gouw, J. A.,
Baumann, K., Edgerton, E. S., Feiner, P. A., Zhang, L., Miller, D. O., Brune, W. H., and Shepson, P. B.: Observation of isoprene hydroxynitrates
in the southeastern United States and implications for the fate of NOx, Atmos. Chem. Phys., 15, 11257–11272, https://doi.org/10.5194/acp-15-11257-2015, 2015.
Xu, J. Z., Zhang, Q., Wang, Z. B., Yu, G. M., Ge, X. L., and Qin, X.: Chemical composition and size distribution of summertime PM2.5
at a high altitude remote location in the northeast of the Qinghai-Xizang (Tibet) Plateau: insights into aerosol sources and processing
in free troposphere, Atmos. Chem. Phys., 15, 5069–5081, https://doi.org/10.5194/acp-15-5069-2015, 2015.
Xu, L., Guo, H., Boyd, C. M., Klein, M., Bougiatioti, A., Cerully, K. M.,
Hite, J. R., Isaacman-VanWertz, G., Kreisberg, N. M., Knote, C., Olson, K.,
Koss, A., Goldstein, A. H., Hering, S. V., de Gouw, J., Baumann, K., Lee,
S.-H., Nenes, A., Weber, R. J., and Ng, N. L.: Effects of anthropogenic
emissions on aerosol formation from isoprene and monoterpenes in the
southeastern United States, P. Natl. Acad. Sci. USA, 112, 37–42,
2015a.
Xu, L., Suresh, S., Guo, H., Weber, R. J., and Ng, N. L.: Aerosol characterization over the southeastern United States using high-resolution
aerosol mass spectrometry: spatial and seasonal variation of aerosol composition and sources with a focus on organic nitrates,
Atmos. Chem. Phys., 15, 7307–7336, https://doi.org/10.5194/acp-15-7307-2015, 2015b.
Xu, L., Guo, H., Weber, R. J., and Ng, N. L.: Chemical characterization of
water-soluble organic aerosol in contrasting rural and urban environments in
the southeastern United States, Environ. Sci. Technol., 51, 78–88, 2017.
Zaveri, R. A., Barnard, J. C., Easter, R. C., Riemer, N., and West, M.:
Particle-resolved simulation of aerosol size, composition, mixing state, and
the associated optical and cloud condensation nuclei activation properties in
an evolving urban plume, J. Geophys. Res.-Atmos., 115, D17210,
https://doi.org/10.1029/2009JD013616, 2010.
Zhang, H., Yee, L. D., Lee, B. H., Curtis, M. P., Worton, D. R.,
Isaacman-VanWertz, G., Offenberg, J. H., Lewandowski, M., Kleindienst, T.
E., and Beaver, M. R.: Monoterpenes are the largest source of summertime
organic aerosol in the southeastern United States, P. Natl. Acad. Sci. USA, 115, 2038–2043, 2018.
Zhang, R., Khalizov, A. F., Pagels, J., Zhang, D., Xue, H., and McMurry, P.
H.: Variability in morphology, hygroscopicity, and optical properties of
soot aerosols during atmospheric processing, P. Natl. Acad. Sci. USA, 105, 10291–10296, 2008.
Zhang, Y., Chen, Y., Lambe, A. T., Olson, N. E., Lei, Z., Craig, R. L.,
Zhang, Z., Gold, A., Onasch, T. B., Jayne, J. T., Worsnop, D. R., Gaston, C.
J., Thornton, J. A., Vizuete, W., Ault, A. P., and Surratt, J. D.: Effect of
Aerosol-Phase State on Secondary Organic Aerosol Formation from the Reactive
Uptake of Isoprene-Derived Epoxydiols (IEPOX), Environ. Sci. Tech. Let., 5,
167–174, 2018.
Short summary
To determine important sources of aerosols during the Southern Oxidant and Aerosol Study (SOAS), as well as their mixing with secondary species, individual particles were analyzed with electron and X-ray microscopy to determine size and chemical composition. Secondary organic aerosol, sea spray aerosol, and mineral dust each dominated during different periods. Particles were less similar chemically to each other than is commonly assumed, which is important for air quality and climate models.
To determine important sources of aerosols during the Southern Oxidant and Aerosol Study (SOAS),...
Altmetrics
Final-revised paper
Preprint