Articles | Volume 19, issue 3
https://doi.org/10.5194/acp-19-1571-2019
© Author(s) 2019. 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-19-1571-2019
© Author(s) 2019. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Research article
| 
07 Feb 2019
Research article |
| 07 Feb 2019
| 07 Feb 2019
Free tropospheric aerosols at the Mt. Bachelor Observatory: more oxidized and higher sulfate content compared to boundary layer aerosols
Shan Zhou
Department of Environmental Toxicology, University of California, Davis, CA 95616, USA
Sonya Collier
Department of Environmental Toxicology, University of California, Davis, CA 95616, USA
Daniel A. Jaffe
School of Science, Technology, Engineering, and Mathematics, University of Washington Bothell, Bothell, WA, USA
Department of Atmospheric Sciences, University of Washington, Seattle, WA, USA
Department of Environmental Toxicology, University of California, Davis, CA 95616, USA
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Manuscript not accepted for further review
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Junfeng Wang, Jianhuai Ye, Dantong Liu, Yangzhou Wu, Jian Zhao, Weiqi Xu, Conghui Xie, Fuzhen Shen, Jie Zhang, Paul E. Ohno, Yiming Qin, Xiuyong Zhao, Scot T. Martin, Alex K. Y. Lee, Pingqing Fu, Daniel J. Jacob, Qi Zhang, Yele Sun, Mindong Chen, and Xinlei Ge
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We compared the organics in total submicron matter and those coated on BC cores during summertime in Beijing and found large differences between them. Traffic-related OA was associated significantly with BC, while cooking-related OA did not coat BC. In addition, a factor likely originated from primary biomass burning OA was only identified in BC-containing particles. Such a unique BBOA requires further field and laboratory studies to verify its presence and elucidate its properties and impacts.
Lawrence I. Kleinman, Arthur J. Sedlacek III, Kouji Adachi, Peter R. Buseck, Sonya Collier, Manvendra K. Dubey, Anna L. Hodshire, Ernie Lewis, Timothy B. Onasch, Jeffery R. Pierce, John Shilling, Stephen R. Springston, Jian Wang, Qi Zhang, Shan Zhou, and Robert J. Yokelson
Atmos. Chem. Phys., 20, 13319–13341, https://doi.org/10.5194/acp-20-13319-2020, https://doi.org/10.5194/acp-20-13319-2020, 2020
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Jianjun Li, Gehui Wang, Qi Zhang, Jin Li, Can Wu, Wenqing Jiang, Tong Zhu, and Limin Zeng
Atmos. Chem. Phys., 19, 10481–10496, https://doi.org/10.5194/acp-19-10481-2019, https://doi.org/10.5194/acp-19-10481-2019, 2019
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Weiqi Xu, Conghui Xie, Eleni Karnezi, Qi Zhang, Junfeng Wang, Spyros N. Pandis, Xinlei Ge, Jingwei Zhang, Junling An, Qingqing Wang, Jian Zhao, Wei Du, Yanmei Qiu, Wei Zhou, Yao He, Ying Li, Jie Li, Pingqing Fu, Zifa Wang, Douglas R. Worsnop, and Yele Sun
Atmos. Chem. Phys., 19, 10205–10216, https://doi.org/10.5194/acp-19-10205-2019, https://doi.org/10.5194/acp-19-10205-2019, 2019
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Xinghua Zhang, Jianzhong Xu, Shichang Kang, Qi Zhang, and Junying Sun
Atmos. Chem. Phys., 19, 7897–7911, https://doi.org/10.5194/acp-19-7897-2019, https://doi.org/10.5194/acp-19-7897-2019, 2019
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Highly time resolved chemistry and sources of PM1 were measured by an Aerodyne HR-ToF-AMS at Waliguan Baseline Observatory, a high-altitude background station at the northeastern edge of Qinghai–Tibet Plateau (QTP), during summer 2017. Relatively higher mass concentration of PM1 and dominant sulfate contribution were observed in this site compared to those at other high-elevation sites in the southern or central QTP, indicating the different aerosol sources between them.
Richie Kaur, Jacqueline R. Labins, Scarlett S. Helbock, Wenqing Jiang, Keith J. Bein, Qi Zhang, and Cort Anastasio
Atmos. Chem. Phys., 19, 6579–6594, https://doi.org/10.5194/acp-19-6579-2019, https://doi.org/10.5194/acp-19-6579-2019, 2019
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We measured hydroxyl radical (•OH), singlet oxygen (1O2*), and organic triplets (3C*) in illuminated aqueous particle extracts. After measuring the impact of dilution on oxidant concentrations, we extrapolated our results to predict them in ambient particles – 1O2* and 3C* concentrations appear to be greatly enhanced, while •OH appears largely unchanged. Two of these oxidants (1O2*, 3C*) are not yet included in atmospheric models, and our results make it possible to include them in the future.
Peng Sun, Wei Nie, Xuguang Chi, Yuning Xie, Xin Huang, Zheng Xu, Ximeng Qi, Zhengning Xu, Lei Wang, Tianyi Wang, Qi Zhang, and Aijun Ding
Atmos. Chem. Phys., 18, 17177–17190, https://doi.org/10.5194/acp-18-17177-2018, https://doi.org/10.5194/acp-18-17177-2018, 2018
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A total of 2 years of online measurement of particulate nitrate was conducted at the SORPES station in the western Yangtze River Delta, eastern China. Nitrate was found to be the major driver of haze pollution and behaved differently in different seasons. In summer, thermodynamic equilibrium and photochemical processes controlled nitrate formation. In winter, N2O5 hydrolysis was demonstrated to be a major contributor to the nitrate episodes.
Arlene M. Fiore, Emily V. Fischer, George P. Milly, Shubha Pandey Deolal, Oliver Wild, Daniel A. Jaffe, Johannes Staehelin, Olivia E. Clifton, Dan Bergmann, William Collins, Frank Dentener, Ruth M. Doherty, Bryan N. Duncan, Bernd Fischer, Stefan Gilge, Peter G. Hess, Larry W. Horowitz, Alexandru Lupu, Ian A. MacKenzie, Rokjin Park, Ludwig Ries, Michael G. Sanderson, Martin G. Schultz, Drew T. Shindell, Martin Steinbacher, David S. Stevenson, Sophie Szopa, Christoph Zellweger, and Guang Zeng
Atmos. Chem. Phys., 18, 15345–15361, https://doi.org/10.5194/acp-18-15345-2018, https://doi.org/10.5194/acp-18-15345-2018, 2018
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We demonstrate a proof-of-concept approach for applying northern midlatitude mountaintop peroxy acetyl nitrate (PAN) measurements and a multi-model ensemble during April to constrain the influence of continental-scale anthropogenic precursor emissions on PAN. Our findings imply a role for carefully coordinated multi-model ensembles in helping identify observations for discriminating among widely varying (and poorly constrained) model responses of atmospheric constituents to changes in emissions.
Jean J. Guo, Arlene M. Fiore, Lee T. Murray, Daniel A. Jaffe, Jordan L. Schnell, Charles T. Moore, and George P. Milly
Atmos. Chem. Phys., 18, 12123–12140, https://doi.org/10.5194/acp-18-12123-2018, https://doi.org/10.5194/acp-18-12123-2018, 2018
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We use the GEOS-Chem model to estimate the influence from anthropogenic and background sources to ozone over the USA. Novel findings include the point that year-to-year background variability on the 10 highest observed ozone days is driven mainly by natural sources and not international or intercontinental pollution transport. High positive model biases during summer are associated with regional ozone production. The EPA 3-year average metric falls short of its aim to remove natural variability.
Yele Sun, Weiqi Xu, Qi Zhang, Qi Jiang, Francesco Canonaco, André S. H. Prévôt, Pingqing Fu, Jie Li, John Jayne, Douglas R. Worsnop, and Zifa Wang
Atmos. Chem. Phys., 18, 8469–8489, https://doi.org/10.5194/acp-18-8469-2018, https://doi.org/10.5194/acp-18-8469-2018, 2018
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We present a 2–year analysis of organic aerosol (OA) from highly time–resolved measurements by an aerosol chemical speciation monitor in the megacity of Beijing. The sources of OA were analyzed with the advanced factor analysis of a multilinear engine (ME-2). Our results showed very different seasonal patterns, relative humidity and temperature dependence, and sources regions among different OA factors. The sources and processes of OA factors, and their roles in haze pollution are elucidated.
Hwajin Kim, Qi Zhang, and Jongbae Heo
Atmos. Chem. Phys., 18, 7149–7168, https://doi.org/10.5194/acp-18-7149-2018, https://doi.org/10.5194/acp-18-7149-2018, 2018
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Aerosol chemistry, sources and processes driving the observed temporal and diurnal variations of PM were studied in the Seoul Metropolitan Area (SMA) during spring 2016. An in-depth analysis of the data uncovered that air quality in SMA was influenced strongly by secondary aerosol formation. Also, it was found that the haze episode during spring was mainly caused by a combination of both regional and local factors, which is different from the winter haze mainly caused by intense local sources.
Dean B. Atkinson, Mikhail Pekour, Duli Chand, James G. Radney, Katheryn R. Kolesar, Qi Zhang, Ari Setyan, Norman T. O'Neill, and Christopher D. Cappa
Atmos. Chem. Phys., 18, 5499–5514, https://doi.org/10.5194/acp-18-5499-2018, https://doi.org/10.5194/acp-18-5499-2018, 2018
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Xinghua Zhang, Jianzhong Xu, Shichang Kang, Yanmei Liu, and Qi Zhang
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Highly time and chemically resolved submicron aerosol properties were characterized online for the first time in a high-altitude site (Qomolangma station, 4276 m a.s.l.) in the northern Himalayas by using the Aerodyne HR-ToF-AMS. Biomass burning plumes were frequently observed and the dynamic processes (emissions, transport, and chemical processing) were characterized. The source and chemical composition of organic aerosol were further elucidated using positive matrix factorization analysis.
Jianzhong Xu, Qi Zhang, Jinsen Shi, Xinlei Ge, Conghui Xie, Junfeng Wang, Shichang Kang, Ruixiong Zhang, and Yuhang Wang
Atmos. Chem. Phys., 18, 427–443, https://doi.org/10.5194/acp-18-427-2018, https://doi.org/10.5194/acp-18-427-2018, 2018
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This manuscript presents results from a comprehensive field study using an HR-AMS coupled with a suite of other instruments in central Tibetan Plateau. The study discusses the chemical composition, sources, and processes of submicron aerosol during the transition from pre-monsoon to monsoon. Organic aerosol was overall highly oxidized during the entire study with higher O / C ratios during the pre-monsoon period. Sensitivity of air pollution transport with synoptic process was also evaluated.
Gouri Prabhakar, Caroline L. Parworth, Xiaolu Zhang, Hwajin Kim, Dominique E. Young, Andreas J. Beyersdorf, Luke D. Ziemba, John B. Nowak, Timothy H. Bertram, Ian C. Faloona, Qi Zhang, and Christopher D. Cappa
Atmos. Chem. Phys., 17, 14747–14770, https://doi.org/10.5194/acp-17-14747-2017, https://doi.org/10.5194/acp-17-14747-2017, 2017
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This work assesses the processes that control the ambient concentrations of particulate nitrate in the the wintertime San Joaquin Valley of California through a combination of aircraft and surface measurements made during the DISCOVER-AQ study. We provide an observational demonstration of how nocturnal production and advection in aloft layers combines with daytime production and loss from entrainment and deposition to give rise to a distinct diurnal profile in surface nitrate concentrations.
Benjamin N. Murphy, Matthew C. Woody, Jose L. Jimenez, Ann Marie G. Carlton, Patrick L. Hayes, Shang Liu, Nga L. Ng, Lynn M. Russell, Ari Setyan, Lu Xu, Jeff Young, Rahul A. Zaveri, Qi Zhang, and Havala O. T. Pye
Atmos. Chem. Phys., 17, 11107–11133, https://doi.org/10.5194/acp-17-11107-2017, https://doi.org/10.5194/acp-17-11107-2017, 2017
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We incorporate recent findings about the behavior of organic pollutants in urban airsheds into the Community Multiscale Air Quality (CMAQ) model to refine predictions of organic particulate pollution in the United States. The new techniques, which account for the volatility and ongoing chemistry of airborne organic compounds, substantially reduce biases, particularly in the winter time and near emission sources.
Jinghao Zhai, Xiaohui Lu, Ling Li, Qi Zhang, Ci Zhang, Hong Chen, Xin Yang, and Jianmin Chen
Atmos. Chem. Phys., 17, 7481–7493, https://doi.org/10.5194/acp-17-7481-2017, https://doi.org/10.5194/acp-17-7481-2017, 2017
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The effective density, chemical composition, and optical properties of particles produced by burning rice straw were measured. Density distribution and single-particle mass spectrometry showed the size-dependent external mixing of black carbon, organic carbon, and potassium salts in biomass burning particles. Optical measurements indicated the significant presence of brown carbon in all particles. Though freshly emitted, light absorption enhancement was observed for particles larger than 200 nm.
Johannes Bieser, Franz Slemr, Jesse Ambrose, Carl Brenninkmeijer, Steve Brooks, Ashu Dastoor, Francesco DeSimone, Ralf Ebinghaus, Christian N. Gencarelli, Beate Geyer, Lynne E. Gratz, Ian M. Hedgecock, Daniel Jaffe, Paul Kelley, Che-Jen Lin, Lyatt Jaegle, Volker Matthias, Andrei Ryjkov, Noelle E. Selin, Shaojie Song, Oleg Travnikov, Andreas Weigelt, Winston Luke, Xinrong Ren, Andreas Zahn, Xin Yang, Yun Zhu, and Nicola Pirrone
Atmos. Chem. Phys., 17, 6925–6955, https://doi.org/10.5194/acp-17-6925-2017, https://doi.org/10.5194/acp-17-6925-2017, 2017
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We conducted a multi model study to investigate our ability to reproduce the vertical distribution of mercury in the atmosphere. For this, we used observational data from over 40 aircraft flights in EU and US. We compared observations to the results of seven chemistry transport models and found that the models are able to reproduce vertical gradients of total and elemental Hg. Finally, we found that different chemical reactions seem responsible for the oxidation of Hg depending on altitude.
Haiyan Li, Qi Zhang, Qiang Zhang, Chunrong Chen, Litao Wang, Zhe Wei, Shan Zhou, Caroline Parworth, Bo Zheng, Francesco Canonaco, André S. H. Prévôt, Ping Chen, Hongliang Zhang, Timothy J. Wallington, and Kebin He
Atmos. Chem. Phys., 17, 4751–4768, https://doi.org/10.5194/acp-17-4751-2017, https://doi.org/10.5194/acp-17-4751-2017, 2017
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The sources and aerosol evolution processes of severe pollution episodes were investigated in Handan during wintertime using real-time measurements. An in-depth analysis of the data uncovered that primary emissions from coal combustion and biomass burning together with secondary formation of sulfate (mainly from SO2 emitted by coal combustion) are important driving factors for haze evolution. Our findings provide useful insights into air pollution control in heavily polluted regions.
Andrew D. Teakles, Rita So, Bruce Ainslie, Robert Nissen, Corinne Schiller, Roxanne Vingarzan, Ian McKendry, Anne Marie Macdonald, Daniel A. Jaffe, Allan K. Bertram, Kevin B. Strawbridge, W. Richard Leaitch, Sarah Hanna, Desiree Toom, Jonathan Baik, and Lin Huang
Atmos. Chem. Phys., 17, 2593–2611, https://doi.org/10.5194/acp-17-2593-2017, https://doi.org/10.5194/acp-17-2593-2017, 2017
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We present a case study of an intense wildfire smoke plume from Siberia that affected the air quality across the Pacific Northwest on 6–10 July 2012. The transport, entrainment, and chemical composition of the plume are examined to characterize the event. Ambient O3 and PM2.5 from surface monitoring is contrast to modelled baseline air quality estimates to show the overall contribution of the plume to exceedances in O3 and PM2.5 air quality standards and objectives that occurred.
Shan Zhou, Sonya Collier, Daniel A. Jaffe, Nicole L. Briggs, Jonathan Hee, Arthur J. Sedlacek III, Lawrence Kleinman, Timothy B. Onasch, and Qi Zhang
Atmos. Chem. Phys., 17, 2477–2493, https://doi.org/10.5194/acp-17-2477-2017, https://doi.org/10.5194/acp-17-2477-2017, 2017
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Wildfire plumes in the western US were sampled at a high-elevation site in summer 2013. Three distinct BBOA types were identified, representing biomass burning OA with different degrees of atmospheric processing. Analysis of consecutive BB plumes transported from the same fire source showed that photooxidation led to enhanced mass fractions of aged BBOAs but negligible net OA production. A possible reason is that SOA formation was almost entirely balanced by BBOA volatilization during transport.
Hwajin Kim, Qi Zhang, Gwi-Nam Bae, Jin Young Kim, and Seung Bok Lee
Atmos. Chem. Phys., 17, 2009–2033, https://doi.org/10.5194/acp-17-2009-2017, https://doi.org/10.5194/acp-17-2009-2017, 2017
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We discuss characteristics, sources, and size distributions of the PM1 composition and OA components in Seoul, Korea, in winter. The serious pollution observed was caused by a combination of various factors, including meteorological conditions, emissions from local primary sources, secondary formation, and transport of air masses from upwind locations. This will be very useful for enacting effective PM reduction strategies for Korea as well as for the broader northern pan-Eurasian region.
James R. Laing, Daniel A. Jaffe, and Jonathan R. Hee
Atmos. Chem. Phys., 16, 15185–15197, https://doi.org/10.5194/acp-16-15185-2016, https://doi.org/10.5194/acp-16-15185-2016, 2016
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We characterize the aerosol physical and optical properties of biomass burning smoke observed at Mt. Bachelor Observatory in central Oregon during August 2015. We found differences in the light absorption properties of biomass burning aerosol depending on where the fire originated from and how long it was transported to the sampling site. We found that aerosol size distribution was not dependent on transport time but affected the light scattering properties of the aerosol.
Jianzhong Xu, Jinsen Shi, Qi Zhang, Xinlei Ge, Francesco Canonaco, André S. H. Prévôt, Matthias Vonwiller, Sönke Szidat, Jinming Ge, Jianmin Ma, Yanqing An, Shichang Kang, and Dahe Qin
Atmos. Chem. Phys., 16, 14937–14957, https://doi.org/10.5194/acp-16-14937-2016, https://doi.org/10.5194/acp-16-14937-2016, 2016
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This study deployed an AMS field study in Lanzhou, a city in northwestern China, evaluating the chemical composition, sources, and processes of urban aerosols during wintertime. In comparison with the results during summer in Lanzhou, the air pollution during winter was more severe and the sources were more complex. In addition, this paper estimates the contributions of fossil and non-fossil sources of organic carbon to primary and secondary organic carbon using the carbon isotopic method.
Xiao Lu, Lin Zhang, Xu Yue, Jiachen Zhang, Daniel A. Jaffe, Andreas Stohl, Yuanhong Zhao, and Jingyuan Shao
Atmos. Chem. Phys., 16, 14687–14702, https://doi.org/10.5194/acp-16-14687-2016, https://doi.org/10.5194/acp-16-14687-2016, 2016
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Increasing wildfire activities in the mountainous western US may present a challenge for the region to attain a recently revised ozone air quality standard in summer. We quantify the wildfire influence on the ozone variability, trends, and number of high ozone days over this region in summers 1989–2010 using a Lagrangian dispersion model and statistical regression models.
Junfeng Wang, Xinlei Ge, Yanfang Chen, Yafei Shen, Qi Zhang, Yele Sun, Jianzhong Xu, Shun Ge, Huan Yu, and Mindong Chen
Atmos. Chem. Phys., 16, 9109–9127, https://doi.org/10.5194/acp-16-9109-2016, https://doi.org/10.5194/acp-16-9109-2016, 2016
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Highly time- and chemically resolved submicron aerosol properties were characterized online for the first time during springtime in Nanjing by using the Aerodyne SP-AMS. Both chemical and size information of black carbon together with other aerosol species were simultaneously determined. An in-depth analysis of the data elucidates the sources and evolution processes of the fine aerosols in the YRD region. Our findings are valuable for air quality remediation in the densely populated regions.
Yele Sun, Wei Du, Pingqing Fu, Qingqing Wang, Jie Li, Xinlei Ge, Qi Zhang, Chunmao Zhu, Lujie Ren, Weiqi Xu, Jian Zhao, Tingting Han, Douglas R. Worsnop, and Zifa Wang
Atmos. Chem. Phys., 16, 8309–8329, https://doi.org/10.5194/acp-16-8309-2016, https://doi.org/10.5194/acp-16-8309-2016, 2016
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We have a comprehensive characterization of the sources, variations and processes of submicron aerosols in Beijing in winter using HR-AMS and GC/MS measurements. The primary sources including traffic, cooking, biomass burning and coal combustion emissions, and secondary components were separated and quantified with PMF. Our results elucidated the important roles of primary emissions, particularly coal combustion, and aqueous-phase processing in the formation of severe air pollution in winter.
Kimiko M. Sakamoto, James R. Laing, Robin G. Stevens, Daniel A. Jaffe, and Jeffrey R. Pierce
Atmos. Chem. Phys., 16, 7709–7724, https://doi.org/10.5194/acp-16-7709-2016, https://doi.org/10.5194/acp-16-7709-2016, 2016
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We determine how various meteorological and fire factors contribute to shaping the aged biomass-burning particle size distribution through coagulation. The mass emissions flux, fire area, and wind speed are dominant factors controlling the aged size distribution. We parameterize the aged size distribution for global/regional aerosol models. We estimate that the aged biomass-burning particle size distribution may be more sensitive to variability in coagulation than SOA formation.
Christopher D. Cappa, Katheryn R. Kolesar, Xiaolu Zhang, Dean B. Atkinson, Mikhail S. Pekour, Rahul A. Zaveri, Alla Zelenyuk, and Qi Zhang
Atmos. Chem. Phys., 16, 6511–6535, https://doi.org/10.5194/acp-16-6511-2016, https://doi.org/10.5194/acp-16-6511-2016, 2016
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Measurements of size-dependent aerosol optical properties at visible wavelengths made during the 2010 CARES study are reported on, with a special focus on the characterization of supermicron particles. The relationships with and dependence upon particle composition, particle size, photochemical aging, water uptake and heating are discussed, along with broader implications of these in situ measurements for the interpretation of remote sensing products.
Colleen P. Jones, Seth N. Lyman, Daniel A. Jaffe, Tanner Allen, and Trevor L. O'Neil
Atmos. Meas. Tech., 9, 2195–2205, https://doi.org/10.5194/amt-9-2195-2016, https://doi.org/10.5194/amt-9-2195-2016, 2016
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Current measurement methods do not provide information about the speciation of oxidized mercury compounds in the atmosphere, leading to uncertainty about which mercury compounds exist and how oxidized mercury is formed. We have developed a gas chromatography/mass spectrometry-based system for identification of oxidized mercury compounds. We discuss the main features and performance of this system.
Dominique E. Young, Hwajin Kim, Caroline Parworth, Shan Zhou, Xiaolu Zhang, Christopher D. Cappa, Roger Seco, Saewung Kim, and Qi Zhang
Atmos. Chem. Phys., 16, 5427–5451, https://doi.org/10.5194/acp-16-5427-2016, https://doi.org/10.5194/acp-16-5427-2016, 2016
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Aerosol chemistry and the sources and processes driving the observed temporal and diurnal variations of PM were studied in a polluted urban environment during winter 2013. These results were compared to a similar campaign from winter 2010. Meteorology strongly influenced PM composition, both directly and indirectly. Nighttime reactions played a more important role in 2013 and the influence from a nighttime formed residual layer that mixed down in the morning was also much more intense in 2013.
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
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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.
S. E. Pusede, K. C. Duffey, A. A. Shusterman, A. Saleh, J. L. Laughner, P. J. Wooldridge, Q. Zhang, C. L. Parworth, H. Kim, S. L. Capps, L. C. Valin, C. D. Cappa, A. Fried, J. Walega, J. B. Nowak, A. J. Weinheimer, R. M. Hoff, T. A. Berkoff, A. J. Beyersdorf, J. Olson, J. H. Crawford, and R. C. Cohen
Atmos. Chem. Phys., 16, 2575–2596, https://doi.org/10.5194/acp-16-2575-2016, https://doi.org/10.5194/acp-16-2575-2016, 2016
L. Kleinman, C. Kuang, A. Sedlacek, G. Senum, S. Springston, J. Wang, Q. Zhang, J. Jayne, J. Fast, J. Hubbe, J. Shilling, and R. Zaveri
Atmos. Chem. Phys., 16, 1729–1746, https://doi.org/10.5194/acp-16-1729-2016, https://doi.org/10.5194/acp-16-1729-2016, 2016
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Atmospheric measurements of total organic aerosol (OA) and tracers of anthropogenic and biogenic emissions are used to quantify synergistic effects (A–B interactions) between two classes of precursors in the formation of OA. Regressions are consistent with the Sacramento plume composed mainly of modern carbon, and OA correlating best with an anthropogenic tracer. It is found that meteorological conditions during a pollution episode can mimic effects of A–B interactions.
V. Shah, L. Jaeglé, L. E. Gratz, J. L. Ambrose, D. A. Jaffe, N. E. Selin, S. Song, T. L. Campos, F. M. Flocke, M. Reeves, D. Stechman, M. Stell, J. Festa, J. Stutz, A. J. Weinheimer, D. J. Knapp, D. D. Montzka, G. S. Tyndall, E. C. Apel, R. S. Hornbrook, A. J. Hills, D. D. Riemer, N. J. Blake, C. A. Cantrell, and R. L. Mauldin III
Atmos. Chem. Phys., 16, 1511–1530, https://doi.org/10.5194/acp-16-1511-2016, https://doi.org/10.5194/acp-16-1511-2016, 2016
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We present airborne observations of mercury over the southeastern USA during summer. Higher concentrations of oxidized mercury were observed in clean, dry air masses descending in the subtropical anti-cyclones. We used an atmospheric model to simulate the chemistry and transport of mercury. We found reasonable agreement with the observations when the modeled oxidation of elemental mercury was increased, suggesting fast cycling between elemental and oxidized mercury.
C. Chen, Y. L. Sun, W. Q. Xu, W. Du, L. B. Zhou, T. T. Han, Q. Q. Wang, P. Q. Fu, Z. F. Wang, Z. Q. Gao, Q. Zhang, and D. R. Worsnop
Atmos. Chem. Phys., 15, 12879–12895, https://doi.org/10.5194/acp-15-12879-2015, https://doi.org/10.5194/acp-15-12879-2015, 2015
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A comprehensive characterization of submicron aerosol composition and sources at 260m in urban Beijing during APEC 2014 is presented. Aerosol species were shown to decrease substantially by 40–80% during APEC, whereas the bulk composition was relatively similar to the result of synergetic controls of secondary precursors. Our results elucidated that the good air quality during APEC was the combined result of emission controls and meteorological effects, with the former playing the dominant role.
A. Lupascu, R. Easter, R. Zaveri, M. Shrivastava, M. Pekour, J. Tomlinson, Q. Yang, H. Matsui, A. Hodzic, Q. Zhang, and J. D. Fast
Atmos. Chem. Phys., 15, 12283–12313, https://doi.org/10.5194/acp-15-12283-2015, https://doi.org/10.5194/acp-15-12283-2015, 2015
Y. L. Sun, Z. F. Wang, W. Du, Q. Zhang, Q. Q. Wang, P. Q. Fu, X. L. Pan, J. Li, J. Jayne, and D. R. Worsnop
Atmos. Chem. Phys., 15, 10149–10165, https://doi.org/10.5194/acp-15-10149-2015, https://doi.org/10.5194/acp-15-10149-2015, 2015
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We conducted the first long-term real-time measurement of submicron aerosol composition in Beijing using an ACSM for 1 year. The seasonal variations of mass concentrations and chemical composition of submicron aerosol were investigated in detail, and the meteorological effects on aerosol chemistry, particularly temperature and relative humidity, were elucidated. Finally, the potential source areas of aerosol species during four seasons were identified.
S. Song, N. E. Selin, A. L. Soerensen, H. Angot, R. Artz, S. Brooks, E.-G. Brunke, G. Conley, A. Dommergue, R. Ebinghaus, T. M. Holsen, D. A. Jaffe, S. Kang, P. Kelley, W. T. Luke, O. Magand, K. Marumoto, K. A. Pfaffhuber, X. Ren, G.-R. Sheu, F. Slemr, T. Warneke, A. Weigelt, P. Weiss-Penzias, D. C. Wip, and Q. Zhang
Atmos. Chem. Phys., 15, 7103–7125, https://doi.org/10.5194/acp-15-7103-2015, https://doi.org/10.5194/acp-15-7103-2015, 2015
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A better knowledge of mercury (Hg) emission fluxes into the global atmosphere is important for assessing its human health impacts and evaluating the effectiveness of corresponding policy actions. We for the first time apply a top-down approach at a global scale to quantitatively estimate present-day mercury emission sources as well as key parameters in a chemical transport model, in order to better constrain the global biogeochemical cycle of mercury.
J. Z. Xu, Q. Zhang, Z. B. Wang, G. M. Yu, X. L. Ge, and X. Qin
Atmos. Chem. Phys., 15, 5069–5081, https://doi.org/10.5194/acp-15-5069-2015, https://doi.org/10.5194/acp-15-5069-2015, 2015
D. B. Atkinson, J. G. Radney, J. Lum, K. R. Kolesar, D. J. Cziczo, M. S. Pekour, Q. Zhang, A. Setyan, A. Zelenyuk, and C. D. Cappa
Atmos. Chem. Phys., 15, 4045–4061, https://doi.org/10.5194/acp-15-4045-2015, https://doi.org/10.5194/acp-15-4045-2015, 2015
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This work describes an analysis of measurements of the influence of water uptake on the light-scattering properties of sub- and supermicron-sized particles as observed in the Sacramento, CA, USA region during the 2010 CARES field campaign. The observations are used to derive campaign-average effective hygroscopicity parameters for submicron oxygenated organic aerosol and for supermicron particles, and the influence of chloride displacement reactions on particle hygroscopicity is examined.
P. Weiss-Penzias, H. M. Amos, N. E. Selin, M. S. Gustin, D. A. Jaffe, D. Obrist, G.-R. Sheu, and A. Giang
Atmos. Chem. Phys., 15, 1161–1173, https://doi.org/10.5194/acp-15-1161-2015, https://doi.org/10.5194/acp-15-1161-2015, 2015
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Speciated atmospheric Hg measurements from five high-elevation sites were compared with a global mercury model. The comparison confirmed that reactive mercury is formed in dry free tropospheric air from the oxidation of elemental Hg, more so in the summer than in other seasons. Simulations run with OH-O3 oxidation instead of the Br oxidation mechanism compared more closely with observations at desert sites, suggesting future simulations should include multiple reaction mechanisms simultaneously.
L. Yu, J. Smith, A. Laskin, C. Anastasio, J. Laskin, and Q. Zhang
Atmos. Chem. Phys., 14, 13801–13816, https://doi.org/10.5194/acp-14-13801-2014, https://doi.org/10.5194/acp-14-13801-2014, 2014
J. Xu, Q. Zhang, M. Chen, X. Ge, J. Ren, and D. Qin
Atmos. Chem. Phys., 14, 12593–12611, https://doi.org/10.5194/acp-14-12593-2014, https://doi.org/10.5194/acp-14-12593-2014, 2014
F. L. Herron-Thorpe, G. H. Mount, L. K. Emmons, B. K. Lamb, D. A. Jaffe, N. L. Wigder, S. H. Chung, R. Zhang, M. D. Woelfle, and J. K. Vaughan
Atmos. Chem. Phys., 14, 12533–12551, https://doi.org/10.5194/acp-14-12533-2014, https://doi.org/10.5194/acp-14-12533-2014, 2014
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Wildfire season simulations from an air quality forecast system for the Pacific Northwest were compared to surface monitor observations across the region and NASA Earth Observing System satellite retrievals of plume top, nitrogen dioxide, aerosol optical depth, and carbon monoxide. This study discusses why the Community Multi-scale Air Quality model predictions under-predicted secondary organic aerosol (SOA) production for events when fire emissions were transported large distances.
K. Tsigaridis, N. Daskalakis, M. Kanakidou, P. J. Adams, P. Artaxo, R. Bahadur, Y. Balkanski, S. E. Bauer, N. Bellouin, A. Benedetti, T. Bergman, T. K. Berntsen, J. P. Beukes, H. Bian, K. S. Carslaw, M. Chin, G. Curci, T. Diehl, R. C. Easter, S. J. Ghan, S. L. Gong, A. Hodzic, C. R. Hoyle, T. Iversen, S. Jathar, J. L. Jimenez, J. W. Kaiser, A. Kirkevåg, D. Koch, H. Kokkola, Y. H Lee, G. Lin, X. Liu, G. Luo, X. Ma, G. W. Mann, N. Mihalopoulos, J.-J. Morcrette, J.-F. Müller, G. Myhre, S. Myriokefalitakis, N. L. Ng, D. O'Donnell, J. E. Penner, L. Pozzoli, K. J. Pringle, L. M. Russell, M. Schulz, J. Sciare, Ø. Seland, D. T. Shindell, S. Sillman, R. B. Skeie, D. Spracklen, T. Stavrakou, S. D. Steenrod, T. Takemura, P. Tiitta, S. Tilmes, H. Tost, T. van Noije, P. G. van Zyl, K. von Salzen, F. Yu, Z. Wang, Z. Wang, R. A. Zaveri, H. Zhang, K. Zhang, Q. Zhang, and X. Zhang
Atmos. Chem. Phys., 14, 10845–10895, https://doi.org/10.5194/acp-14-10845-2014, https://doi.org/10.5194/acp-14-10845-2014, 2014
J. D. Fast, J. Allan, R. Bahreini, J. Craven, L. Emmons, R. Ferrare, P. L. Hayes, A. Hodzic, J. Holloway, C. Hostetler, J. L. Jimenez, H. Jonsson, S. Liu, Y. Liu, A. Metcalf, A. Middlebrook, J. Nowak, M. Pekour, A. Perring, L. Russell, A. Sedlacek, J. Seinfeld, A. Setyan, J. Shilling, M. Shrivastava, S. Springston, C. Song, R. Subramanian, J. W. Taylor, V. Vinoj, Q. Yang, R. A. Zaveri, and Q. Zhang
Atmos. Chem. Phys., 14, 10013–10060, https://doi.org/10.5194/acp-14-10013-2014, https://doi.org/10.5194/acp-14-10013-2014, 2014
A. Setyan, C. Song, M. Merkel, W. B. Knighton, T. B. Onasch, M. R. Canagaratna, D. R. Worsnop, A. Wiedensohler, J. E. Shilling, and Q. Zhang
Atmos. Chem. Phys., 14, 6477–6494, https://doi.org/10.5194/acp-14-6477-2014, https://doi.org/10.5194/acp-14-6477-2014, 2014
C. Knote, A. Hodzic, J. L. Jimenez, R. Volkamer, J. J. Orlando, S. Baidar, J. Brioude, J. Fast, D. R. Gentner, A. H. Goldstein, P. L. Hayes, W. B. Knighton, H. Oetjen, A. Setyan, H. Stark, R. Thalman, G. Tyndall, R. Washenfelder, E. Waxman, and Q. Zhang
Atmos. Chem. Phys., 14, 6213–6239, https://doi.org/10.5194/acp-14-6213-2014, https://doi.org/10.5194/acp-14-6213-2014, 2014
F. Mei, A. Setyan, Q. Zhang, and J. Wang
Atmos. Chem. Phys., 13, 12155–12169, https://doi.org/10.5194/acp-13-12155-2013, https://doi.org/10.5194/acp-13-12155-2013, 2013
M. Gyawali, W. P. Arnott, R. A. Zaveri, C. Song, M. Pekour, B. Flowers, M. K. Dubey, A. Setyan, Q. Zhang, J. W. Harworth, J. G. Radney, D. B. Atkinson, S. China, C. Mazzoleni, K. Gorkowski, R. Subramanian, B. T. Jobson, and H. Moosmüller
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acpd-13-7113-2013, https://doi.org/10.5194/acpd-13-7113-2013, 2013
Revised manuscript not accepted
Related subject area
Subject: Aerosols | Research Activity: Field Measurements | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Measurement report: Per- and polyfluoroalkyl substances (PFAS) in particulate matter (PM10) from activated sludge aeration
African dust transported to Barbados in the wintertime lacks indicators of chemical aging
A 60-year atmospheric nitrate isotope record from a southeastern Greenland ice core with minimal postdepositional alteration
Measurement report: Characterization of aerosol hygroscopicity over Southeast Asia during the NASA CAMP2Ex campaign
Molecular characterization of organic aerosols in urban and forested areas of Paris using high-resolution mass spectrometry
Measurement report: Wintertime aerosol characterization at an urban traffic site in Helsinki, Finland
Source apportionment and ecotoxicity of PM2.5 pollution events in a major Southern Hemisphere megacity: influence of a biofuel-impacted fleet and biomass burning
Marine organic aerosol at Mace Head: effects from phytoplankton and source region variability
Measurement report: Sources and meteorology influencing highly time-resolved PM2.5 trace elements at three urban sites in the extremely polluted Indo-Gangetic Plain in India
Formation of highly absorptive secondary brown carbon through nighttime multiphase chemistry of biomass burning emissions
Measurement report: Vertically resolved atmospheric properties observed over the Southern Great Plains with the ArcticShark uncrewed aerial system
Technical note: Towards a stronger observational support for haze pollution control by interpreting carbonaceous aerosol results derived from different measurement approaches
Non-biogenic sources are an important but overlooked contributor to aerosol isoprene-derived organosulfates during winter in northern China
The critical role of aqueous-phase processes in aromatic-derived nitrogen-containing organic aerosol formation in cities with different energy consumption patterns
Characterization of atmospheric water-soluble brown carbon in the Athabasca oil sands region, Canada
Sensitivity of aerosol and cloud properties to coupling strength of marine boundary layer clouds over the northwest Atlantic
Measurement Report: Molecular composition, sources, and evolution of atmospheric organic aerosols in a basin city in China
Burning conditions and transportation pathways determine biomass-burning aerosol properties in the Ascension Island marine boundary layer
Observations of high-time-resolution and size-resolved aerosol chemical composition and microphysics in the central Arctic: implications for climate-relevant particle properties
Measurement report: Brown carbon aerosol in rural Germany – sources, chemistry, and diurnal variations
Particle flux-gradient relationships in the high Arctic: Emission and deposition patterns across three surface types
Climatology of aerosol pH and its controlling factors at the Melpitz continental background site in central Europe
Measurement Report: Polycyclic aromatic hydrocarbons (PAHs) and their alkylated (RPAHs), nitrated (NPAHs) and oxygenated (OPAHs) derivatives in the global marine atmosphere: occurrence, spatial variations, and source apportionment
Multiple eco-regions contribute to the seasonal cycle of Antarctic aerosol size distributions
Seasonal investigation of ultrafine-particle organic composition in an eastern Amazonian rainforest
Characterizing lead-rich particles in Beijing's atmosphere following coal-to-gas conversion: Insights from single particle aerosol mass spectrometry
Contrasting solubility and speciation of metal ions in total suspended particulate matter and fog from the coast of Namibia
Significant secondary formation of nitrogenous organic aerosols in an urban atmosphere revealed by bihourly measurements of bulk organic nitrogen and comprehensive molecular markers
High-resolution analyses of concentrations and sizes of refractory black carbon particles deposited in northwestern Greenland over the past 350 years – Part 2: Seasonal and temporal trends in refractory black carbon originated from fossil fuel combustion and biomass burning
Direct measurement of N2O5 heterogeneous uptake coefficients on atmospheric aerosols in southwestern China and evaluation of current parameterizations
Significant role of biomass burning in heavy haze formation in Nanjing, a megacity in China: molecular-level insights from intensive PM2.5 sampling on winter hazy days
Widespread trace bromine and iodine in remote tropospheric non-sea-salt aerosols
Significant contributions of biomass burning to PM2.5-bound aromatic compounds: insights from field observations and quantum chemical calculations
Iron isotopes reveal significant aerosol dissolution over the Pacific Ocean
Formation and chemical evolution of secondary organic aerosol in two different environments: a dual-chamber study
Complementary aerosol mass spectrometry elucidates sources of wintertime sub-micron particle pollution in Fairbanks, Alaska, during ALPACA 2022
Enrichment of organic nitrogen in fog residuals observed in the Italian Po Valley
Technical note: Quantified organic aerosol subsaturated hygroscopicity by a simple optical scatter monitor system through field measurements
Measurement report: Oxidation potential of water-soluble aerosol components in the south and north of Beijing
Enhanced daytime secondary aerosol formation driven by gas–particle partitioning in downwind urban plumes
Technical note: Reconstructing surface missing aerosol elemental carbon data in long-term series with ensemble learning
Understanding the mechanism and importance of brown carbon bleaching across the visible spectrum in biomass burning plumes from the WE-CAN campaign
Influence of terrestrial and marine air mass on the constituents and intermixing of bioaerosols over a coastal atmosphere
A multi-site passive approach to studying the emissions and evolution of smoke from prescribed fires
The annual cycle and sources of relevant aerosol precursor vapors in the central Arctic during the MOSAiC expedition
Enhanced emission of intermediate/semi-volatile organic matters in both gas and particle phases from ship exhausts with low-sulfur fuels
Advances in characterization of black carbon particles and their associated coatings using the soot particle aerosol mass spectrometer in Singapore, a complex city environment
Measurement report: Crustal materials play an increasing role in elevating particle pH: Insights from 12-year records in a typical inland city of China
Opinion: How will advances in aerosol science inform our understanding of the health impacts of outdoor particulate pollution?
Machine Learning Assisted Chemical Characterization and Optical Properties of Atmospheric Brown Carbon in Nanjing, China
Jishnu Pandamkulangara Kizhakkethil, Zongbo Shi, Anna Bogush, and Ivan Kourtchev
Atmos. Chem. Phys., 25, 5947–5958, https://doi.org/10.5194/acp-25-5947-2025, https://doi.org/10.5194/acp-25-5947-2025, 2025
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Pollution with per- and polyfluoroalkyl substances (PFAS) has received attention due to their environmental persistence and bioaccumulation, but their sources remain poorly understood. PM10 (particulate matter) collected above a scaled-down activated sludge tank treating domestic sewage in the UK was analysed for a range of short-, medium-, and long-chain PFAS. Eight PFAS were detected in the PM10. Our results suggest that wastewater treatment processes, i.e. activated sludge aeration, could aerosolise PFAS into airborne PM.
Haley M. Royer, Michael T. Sheridan, Hope E. Elliott, Edmund Blades, Nurun Nahar Lata, Zezhen Cheng, Swarup China, Zihua Zhu, Andrew P. Ault, and Cassandra J. Gaston
Atmos. Chem. Phys., 25, 5743–5759, https://doi.org/10.5194/acp-25-5743-2025, https://doi.org/10.5194/acp-25-5743-2025, 2025
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Saharan dust transported across the Atlantic to the Caribbean, South America, and North America is hypothesized to undergo chemical processing by acids that enhances cloud droplet formation and nutrient availability. In this study, chemical analysis performed on African dust deposited over Barbados shows that acid tracers are found mostly on sea salt and smoke particles, rather than dust, indicating that dust particles undergo minimal chemical processing.
Zhao Wei, Shohei Hattori, Asuka Tsuruta, Zhuang Jiang, Sakiko Ishino, Koji Fujita, Sumito Matoba, Lei Geng, Alexis Lamothe, Ryu Uemura, Naohiro Yoshida, Joel Savarino, and Yoshinori Iizuka
Atmos. Chem. Phys., 25, 5727–5742, https://doi.org/10.5194/acp-25-5727-2025, https://doi.org/10.5194/acp-25-5727-2025, 2025
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Nitrate isotope records in ice cores reveal changes in NOₓ emissions and atmospheric oxidation chemistry driven by human activity. However, UV-driven postdepositional processes can alter nitrate in snow, making snow accumulation rates critical for preserving these records. This study examines nitrate isotopes in a southeastern Greenland ice core, where high snow accumulation minimizes these effects, providing a reliable archive of atmospheric nitrogen cycling.
Genevieve Rose Lorenzo, Luke D. Ziemba, Avelino F. Arellano, Mary C. Barth, Ewan C. Crosbie, Joshua P. DiGangi, Glenn S. Diskin, Richard Ferrare, Miguel Ricardo A. Hilario, Michael A. Shook, Simone Tilmes, Jian Wang, Qian Xiao, Jun Zhang, and Armin Sorooshian
Atmos. Chem. Phys., 25, 5469–5495, https://doi.org/10.5194/acp-25-5469-2025, https://doi.org/10.5194/acp-25-5469-2025, 2025
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Novel aerosol hygroscopicity analyses of CAMP2Ex (Cloud, Aerosol, and Monsoon Processes Philippines Experiment) field campaign data show low aerosol hygroscopicity values in Southeast Asia. Organic carbon from smoke decreases hygroscopicity to levels more like those in continental than in polluted marine regions. Hygroscopicity changes at cloud level demonstrate how surface particles impact clouds in the region, affecting model representation of aerosol and cloud interactions in similar polluted marine regions with high organic carbon emissions.
Diana L. Pereira, Chiara Giorio, Aline Gratien, Alexander Zherebker, Gael Noyalet, Servanne Chevaillier, Stéphanie Alage, Elie Almarj, Antonin Bergé, Thomas Bertin, Mathieu Cazaunau, Patrice Coll, Ludovico Di Antonio, Sergio Harb, Johannes Heuser, Cécile Gaimoz, Oscar Guillemant, Brigitte Language, Olivier Lauret, Camilo Macias, Franck Maisonneuve, Bénédicte Picquet-Varrault, Raquel Torres, Sylvain Triquet, Pascal Zapf, Lelia Hawkins, Drew Pronovost, Sydney Riley, Pierre-Marie Flaud, Emilie Perraudin, Pauline Pouyes, Eric Villenave, Alexandre Albinet, Olivier Favez, Robin Aujay-Plouzeau, Vincent Michoud, Christopher Cantrell, Manuela Cirtog, Claudia Di Biagio, Jean-François Doussin, and Paola Formenti
Atmos. Chem. Phys., 25, 4885–4905, https://doi.org/10.5194/acp-25-4885-2025, https://doi.org/10.5194/acp-25-4885-2025, 2025
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In order to study aerosols in environments influenced by anthropogenic and biogenic emissions, we performed analyses of samples collected during the ACROSS (Atmospheric Chemistry Of the Suburban Forest) campaign in summer 2022 in the greater Paris area. After analysis of the chemical composition by means of total carbon determination and high-resolution mass spectrometry, this work highlights the influence of anthropogenic inputs on the chemical composition of both urban and forested areas.
Kimmo Teinilä, Sanna Saarikoski, Henna Lintusaari, Teemu Lepistö, Petteri Marjanen, Minna Aurela, Heidi Hellén, Toni Tykkä, Markus Lampimäki, Janne Lampilahti, Luis Barreira, Timo Mäkelä, Leena Kangas, Juha Hatakka, Sami Harni, Joel Kuula, Jarkko V. Niemi, Harri Portin, Jaakko Yli-Ojanperä, Ville Niemelä, Milja Jäppi, Katrianne Lehtipalo, Joonas Vanhanen, Liisa Pirjola, Hanna E. Manninen, Tuukka Petäjä, Topi Rönkkö, and Hilkka Timonen
Atmos. Chem. Phys., 25, 4907–4928, https://doi.org/10.5194/acp-25-4907-2025, https://doi.org/10.5194/acp-25-4907-2025, 2025
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Physical and chemical properties of particulate matter and concentrations of trace gases were measured in a street canyon in Helsinki, Finland, and an urban background site in January–February 2022 to investigate the effect of wintertime conditions on pollutants. State-of-the-art instruments and a mobile laboratory were used, and the measurement data were analysed further with modelling tools like positive matrix factorization and the Pollution Detection Algorithm.
Guilherme Martins Pereira, Leonardo Yoshiaki Kamigauti, Rubens Fabio Pereira, Djacinto Monteiro dos Santos, Thayná da Silva Santos, José Vinicius Martins, Célia Alves, Cátia Gonçalves, Ismael Casotti Rienda, Nora Kováts, Thiago Nogueira, Luciana Rizzo, Paulo Artaxo, Regina Maura de Miranda, Marcia Akemi Yamasoe, Edmilson Dias de Freitas, Pérola de Castro Vasconcellos, and Maria de Fatima Andrade
Atmos. Chem. Phys., 25, 4587–4616, https://doi.org/10.5194/acp-25-4587-2025, https://doi.org/10.5194/acp-25-4587-2025, 2025
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The chemical composition of fine particulate matter was studied in the megacity of São Paulo (Brazil) during a polluted period. Vehicular-related sources remain relevant; however, a high contribution of biomass burning was observed and correlated with sample ecotoxicity. Emerging biomass burning sources, such as forest fires and sugarcane-bagasse-based power plants, highlight the need for additional control measures alongside stricter rules concerning vehicular emissions.
Emmanuel Chevassus, Kirsten N. Fossum, Darius Ceburnis, Lu Lei, Chunshui Lin, Wei Xu, Colin O'Dowd, and Jurgita Ovadnevaite
Atmos. Chem. Phys., 25, 4107–4129, https://doi.org/10.5194/acp-25-4107-2025, https://doi.org/10.5194/acp-25-4107-2025, 2025
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This study presents the first source apportionment of organic aerosol at Mace Head via high-resolution mass spectrometry. Introducing transfer entropy as a novel method reveals that aged organic aerosol originates from both open-ocean ozonolysis and local peat-burning oxidation. Methanesulfonic acid and organic sea spray both mirror phytoplankton activity, with the former closely tied to coccolithophore blooms and the latter linked to diatoms, chlorophytes, and cyanobacteria.
Ashutosh K. Shukla, Sachchida N. Tripathi, Shamitaksha Talukdar, Vishnu Murari, Sreenivas Gaddamidi, Manousos-Ioannis Manousakas, Vipul Lalchandani, Kuldeep Dixit, Vinayak M. Ruge, Peeyush Khare, Mayank Kumar, Vikram Singh, Neeraj Rastogi, Suresh Tiwari, Atul K. Srivastava, Dilip Ganguly, Kaspar Rudolf Daellenbach, and André S. H. Prévôt
Atmos. Chem. Phys., 25, 3765–3784, https://doi.org/10.5194/acp-25-3765-2025, https://doi.org/10.5194/acp-25-3765-2025, 2025
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Our study delves into the elemental composition of aerosols at three sites across the Indo-Gangetic Plain (IGP), revealing distinct patterns during pollution episodes. We found significant increases in chlorine (Cl)-rich and solid fuel combustion (SFC) sources, indicating dynamic emission sources, agricultural burning impacts, and meteorological influences. Surges in Cl-rich particles during cold periods highlight their role in particle growth under high-relative-humidity conditions.
Ye Kuang, Biao Luo, Shan Huang, Junwen Liu, Weiwei Hu, Yuwen Peng, Duohong Chen, Dingli Yue, Wanyun Xu, Bin Yuan, and Min Shao
Atmos. Chem. Phys., 25, 3737–3752, https://doi.org/10.5194/acp-25-3737-2025, https://doi.org/10.5194/acp-25-3737-2025, 2025
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This research reveals the potential importance of nighttime NO3 radical chemistry and aerosol water in the rapid formation of secondary brown carbon from diluted biomass burning emissions. The findings enhance our understanding of nighttime biomass burning evolution and its implications for climate and regional air quality, especially regarding interactions with background aerosol water and water-rich fogs and clouds.
Fan Mei, Qi Zhang, Damao Zhang, Jerome D. Fast, Gourihar Kulkarni, Mikhail S. Pekour, Christopher R. Niedek, Susanne Glienke, Israel Silber, Beat Schmid, Jason M. Tomlinson, Hardeep S. Mehta, Xena Mansoura, Zezhen Cheng, Gregory W. Vandergrift, Nurun Nahar Lata, Swarup China, and Zihua Zhu
Atmos. Chem. Phys., 25, 3425–3444, https://doi.org/10.5194/acp-25-3425-2025, https://doi.org/10.5194/acp-25-3425-2025, 2025
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This study highlights the unique capability of the ArcticShark, an uncrewed aerial system, in measuring vertically resolved atmospheric properties. Data from 32 research flights in 2023 reveal seasonal patterns and correlations with conventional measurements. The consistency and complementarity of in situ and remote sensing methods are highlighted. The study demonstrates the ArcticShark’s versatility in bridging data gaps and improving the understanding of vertical atmospheric structures.
Yuan Cheng, Ying-jie Zhong, Zhi-qing Zhang, Xu-bing Cao, and Jiu-meng Liu
EGUsphere, https://doi.org/10.5194/egusphere-2025-537, https://doi.org/10.5194/egusphere-2025-537, 2025
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As an emerging hotspot of atmospheric sciences, Northeast China is distinct due to the frigid winter and the strong emissions from agricultural fires. Based on field campaigns conducted in Harbin, we successively identified the analytical method that could lead to proper results of organic and elemental carbon. Our results are believed to be a support for future efforts on exploration of the PM2.5 sources in Northeast China, which are essential for further improving the regional air quality.
Ting Yang, Yu Xu, Yu-Chen Wang, Yi-Jia Ma, Hong-Wei Xiao, Hao Xiao, and Hua-Yun Xiao
Atmos. Chem. Phys., 25, 2967–2978, https://doi.org/10.5194/acp-25-2967-2025, https://doi.org/10.5194/acp-25-2967-2025, 2025
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Previous measurement–model comparisons of atmospheric isoprene levels showed a significant unidentified source of isoprene in some northern Chinese cities during winter. Here, the first combination of large-scale observations and field combustion experiments provides novel insights into biomass burning emissions as a significant source of isoprene-derived organosulfates during winter in northern cities of China.
Yi-Jia Ma, Yu Xu, Ting Yang, Lin Gui, Hong-Wei Xiao, Hao Xiao, and Hua-Yun Xiao
Atmos. Chem. Phys., 25, 2763–2780, https://doi.org/10.5194/acp-25-2763-2025, https://doi.org/10.5194/acp-25-2763-2025, 2025
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The abundance, potential precursors, and main formation mechanisms of nitrogen-containing organic compounds (NOCs) in PM2.5 during winter were compared among cities with different energy consumption patterns. The aerosol NOC pollution during winter in China is closely associated with the intensity of precursor emissions and the aqueous-phase processes. Our results highlight the importance of emission reduction strategies in controlling aerosol NOCs pollution during winter in China.
Dane Blanchard, Mark Gordon, Duc Huy Dang, Paul Andrew Makar, and Julian Aherne
Atmos. Chem. Phys., 25, 2423–2442, https://doi.org/10.5194/acp-25-2423-2025, https://doi.org/10.5194/acp-25-2423-2025, 2025
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This study offers the first known evaluation of water-soluble brown carbon aerosols in the Athabasca oil sands region (AOSR), Canada. Fluorescence spectroscopy analysis of aerosol samples from five regional sites (collected during the summer of 2021) identified oil sands operations as a measurable brown carbon source. Industrial aerosol emissions were unlikely to impact regional radiative forcing. These findings show that fluorescence spectroscopy can be used to monitor brown carbon in the AOSR.
Kira Zeider, Kayla McCauley, Sanja Dmitrovic, Leong Wai Siu, Yonghoon Choi, Ewan C. Crosbie, Joshua P. DiGangi, Glenn S. Diskin, Simon Kirschler, John B. Nowak, Michael A. Shook, Kenneth L. Thornhill, Christiane Voigt, Edward L. Winstead, Luke D. Ziemba, Paquita Zuidema, and Armin Sorooshian
Atmos. Chem. Phys., 25, 2407–2422, https://doi.org/10.5194/acp-25-2407-2025, https://doi.org/10.5194/acp-25-2407-2025, 2025
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In situ aircraft data collected over the northwest Atlantic Ocean are utilized to compare aerosol conditions and turbulence between near-surface and below-cloud-base altitudes for different regimes of coupling strength between those two levels, along with how cloud microphysical properties vary across those regimes. Stronger coupling yields more homogenous aerosol structure vertically along with higher cloud drop concentrations and sea salt influence in clouds.
Junke Zhang, Xinyi Fu, Chunying Chen, Yunfei Su, Siyu Liu, Luyao Chen, Yubao Chen, Gehui Wang, and Andre S. H. Prevot
EGUsphere, https://doi.org/10.5194/egusphere-2025-92, https://doi.org/10.5194/egusphere-2025-92, 2025
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The 125 organic aerosol (OA) compounds in PM2.5 in winter in Chengdu were measured at the molecular level. OA was dominated by fatty acids, phthalate esters, and anhydrosugars, and were deeply influenced by anthropogenic sources. As pollution worsens: secondary inorganic species and secondary organic carbon (OC) dominated the increase in PM2.5; fatty acids and anhydrosugars dominated the increase in OA; and the contribution of secondary formation and biomass burning to OC increased markedly.
Amie Dobracki, Ernie R. Lewis, Arthur J. Sedlacek III, Tyler Tatro, Maria A. Zawadowicz, and Paquita Zuidema
Atmos. Chem. Phys., 25, 2333–2363, https://doi.org/10.5194/acp-25-2333-2025, https://doi.org/10.5194/acp-25-2333-2025, 2025
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Biomass-burning aerosol is commonly present in the marine boundary layer over the southeast Atlantic Ocean between June and October. Our research indicates that burning conditions, aerosol transport pathways, and prolonged oxidation processes (heterogeneous and aqueous phases) determine the chemical, microphysical, and optical properties of the boundary layer aerosol. Notably, we find that the aerosol optical properties can be estimated from the chemical properties alone.
Benjamin Heutte, Nora Bergner, Hélène Angot, Jakob B. Pernov, Lubna Dada, Jessica A. Mirrielees, Ivo Beck, Andrea Baccarini, Matthew Boyer, Jessie M. Creamean, Kaspar R. Daellenbach, Imad El Haddad, Markus M. Frey, Silvia Henning, Tiia Laurila, Vaios Moschos, Tuukka Petäjä, Kerri A. Pratt, Lauriane L. J. Quéléver, Matthew D. Shupe, Paul Zieger, Tuija Jokinen, and Julia Schmale
Atmos. Chem. Phys., 25, 2207–2241, https://doi.org/10.5194/acp-25-2207-2025, https://doi.org/10.5194/acp-25-2207-2025, 2025
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Limited aerosol measurements in the central Arctic hinder our understanding of aerosol–climate interactions in the region. Our year-long observations of aerosol physicochemical properties during the MOSAiC expedition reveal strong seasonal variations in aerosol chemical composition, where the short-term variability is heavily affected by storms in the Arctic. Local wind-generated particles are shown to be an important source of cloud seeds, especially in autumn.
Feng Jiang, Harald Saathoff, Uzoamaka Ezenobi, Junwei Song, Hengheng Zhang, Linyu Gao, and Thomas Leisner
Atmos. Chem. Phys., 25, 1917–1930, https://doi.org/10.5194/acp-25-1917-2025, https://doi.org/10.5194/acp-25-1917-2025, 2025
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The chemical composition of brown carbon in the particle and gas phase was determined by mass spectrometry. BrC in the gas phase was mainly controlled by secondary formation and particle-to-gas partitioning. BrC in the particle phase was mainly from secondary formation. This work helps to get a better understanding of diurnal variations and the sources of brown carbon aerosol at a rural location in central Europe.
Theresa Mathes, Heather Guy, John Prytherch, Julia Kojoj, Ian Brooks, Sonja Murto, Paul Zieger, Birgit Wehner, Michael Tjernström, and Andreas Held
EGUsphere, https://doi.org/10.5194/egusphere-2025-183, https://doi.org/10.5194/egusphere-2025-183, 2025
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The Arctic is warming faster than the global average and aerosol-cloud-sea-ice interactions are crucial for studying its climate system. During the ARTofMELT Expedition 2023, particle and sensible heat fluxes were measured over multiple surfaces. Wide lead surfaces acted as particle sources with the strongest sensible heat fluxes, while closed ice surfaces acted as a particle sink. This study improves methods to measure these interactions, enhancing our understanding of Arctic climate processes.
Vikram Pratap, Christopher J. Hennigan, Bastian Stieger, Andreas Tilgner, Laurent Poulain, Dominik van Pinxteren, Gerald Spindler, and Hartmut Herrmann
EGUsphere, https://doi.org/10.5194/egusphere-2025-457, https://doi.org/10.5194/egusphere-2025-457, 2025
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In this work, we characterize trends in aerosol pH and its controlling factors over the period of 2010 – 2019 at the Melpitz research station in eastern Germany. We find strong trends in aerosol pH and major inorganic species in response to changing emissions. We conduct a detailed thermodynamic analysis of the aerosol system and discuss implications for controlling PM2.5 in the region.
Rui Li, Yubing Shen, Yumeng Shao, Yining Gao, Ziwei Yao, Qian Liu, Xing Liu, and Guitao Shi
EGUsphere, https://doi.org/10.5194/egusphere-2024-3740, https://doi.org/10.5194/egusphere-2024-3740, 2025
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It is the first time to reveal the global variations of PAHs derivatives in the marine air. We found that marine aerosols in East China Sea (ECS) and Western Pacific (WP) were significantly affected by coal and engine combustion, while those in Bismarck Sea (BS) and East Australian Sea (EAS) were mainly influenced by wildfire and coal combustion. Antarctic Ocean (AO) was dominated by biomass burning and local shipping emissions. This finding help elucidate the mechanism of global PAH cycle.
James Brean, David C. S. Beddows, Eija Asmi, Aki Virkkula, Lauriane L. J. Quéléver, Mikko Sipilä, Floortje Van Den Heuvel, Thomas Lachlan-Cope, Anna Jones, Markus Frey, Angelo Lupi, Jiyeon Park, Young Jun Yoon, Rolf Weller, Giselle L. Marincovich, Gabriela C. Mulena, Roy M. Harrison, and Manuel Dall'Osto
Atmos. Chem. Phys., 25, 1145–1162, https://doi.org/10.5194/acp-25-1145-2025, https://doi.org/10.5194/acp-25-1145-2025, 2025
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Our results emphasise how understanding the geographical variation in surface types across the Antarctic is key to understanding secondary aerosol sources.
Adam E. Thomas, Hayley S. Glicker, Alex B. Guenther, Roger Seco, Oscar Vega Bustillos, Julio Tota, Rodrigo A. F. Souza, and James N. Smith
Atmos. Chem. Phys., 25, 959–977, https://doi.org/10.5194/acp-25-959-2025, https://doi.org/10.5194/acp-25-959-2025, 2025
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We present measurements of the organic composition of ultrafine particles collected from the eastern Amazon, an understudied region that is subjected to increasing human influence. We find that while isoprene chemistry is likely significant for ultrafine-particle growth throughout the year, compounds related to other sources, such as biological-spore emissions and biomass burning, exhibit striking seasonal differences, implying extensive variation in regional ultrafine-particle sources.
Xiufeng Lian, Yongjiang Xu, Fengxian Liu, Long Peng, Xiaodong Hu, Guigang Tang, Xu Dao, Hui Guo, Liwei Wang, Bo Huang, Chunlei Cheng, Lei Li, Guohua Zhang, Xinhui Bi, Xiaofei Wang, Zhen Zhou, and Mei Li
EGUsphere, https://doi.org/10.5194/egusphere-2024-3469, https://doi.org/10.5194/egusphere-2024-3469, 2025
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In this study, we analyzed the mixing state and atmospheric chemical processes of Pb-rich single particles in Beijing. Then, we focused on analyzing the differences in Pb-rich particles between the heating period and non-heating period, as well as the formation mechanism of lead nitrate after coal-to-gas conversion. Our results highlighted the improvement of coal-to-gas conversion on Pb in the particulate.
Chiara Giorio, Anne Monod, Valerio Di Marco, Pierre Herckes, Denise Napolitano, Amy Sullivan, Gautier Landrot, Daniel Warnes, Marika Nasti, Sara D'Aronco, Agathe Gérardin, Nicolas Brun, Karine Desboeufs, Sylvain Triquet, Servanne Chevaillier, Claudia Di Biagio, Francesco Battaglia, Frédéric Burnet, Stuart J. Piketh, Andreas Namwoonde, Jean-François Doussin, and Paola Formenti
EGUsphere, https://doi.org/10.5194/egusphere-2024-4140, https://doi.org/10.5194/egusphere-2024-4140, 2025
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A comparison between the solubility of trace metals in pairs of total suspended particulate (TSP) and fog water samples collected in Henties Bay, Namibia, during the AEROCLO-sA field campaign is presented. We found enhanced solubility of metals in fog samples which we attributed to metal-ligand complexes formation in the early stages of particle activation into droplets which can then remain in a kinetically stable form in fog or lead to the formation of colloidal nanoparticles.
Xu Yu, Min Zhou, Shuhui Zhu, Liping Qiao, Jinjian Li, Yingge Ma, Zijing Zhang, Kezheng Liao, Hongli Wang, and Jian Zhen Yu
EGUsphere, https://doi.org/10.5194/egusphere-2024-4103, https://doi.org/10.5194/egusphere-2024-4103, 2025
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Online measurements of bulk aerosol organic nitrogen (ON), in conjunction with a comprehensive array of source markers, have revealed five emission sources and five potentially significant formation processes of nitrogenous organic aerosols. This study provides first quantitative source analysis of ON aerosol and valuable observational evidence on secondary ON aerosol formation through NH3 and NOx chemistries.
Kumiko Goto-Azuma, Yoshimi Ogawa-Tsukagawa, Kaori Fukuda, Koji Fujita, Motohiro Hirabayashi, Remi Dallmayr, Jun Ogata, Nobuhiro Moteki, Tatsuhiro Mori, Sho Ohata, Yutaka Kondo, Makoto Koike, Sumito Matoba, Moe Kadota, Akane Tsushima, Naoko Nagatsuka, and Teruo Aoki
Atmos. Chem. Phys., 25, 657–683, https://doi.org/10.5194/acp-25-657-2025, https://doi.org/10.5194/acp-25-657-2025, 2025
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Monthly ice core records spanning 350 years from Greenland show trends in refractory black carbon (rBC) concentrations and sizes. rBC levels have increased since the 1870s due to the inflow of anthropogenic rBC, with larger diameters than those from biomass burning (BB) rBC. High summer BB rBC peaks may reduce the ice sheet albedo, but BB rBC showed no increase until the early 2000s. These results are vital for validating aerosol and climate models.
Jiayin Li, Tianyu Zhai, Xiaorui Chen, Haichao Wang, Shuyang Xie, Shiyi Chen, Chunmeng Li, Huabin Dong, and Keding Lu
EGUsphere, https://doi.org/10.5194/egusphere-2024-3804, https://doi.org/10.5194/egusphere-2024-3804, 2025
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We directly measured the dinitrogen pentoxide (N2O5) uptake coefficient which critical impact the NOx fate and particulate nitrate formation in a typical highland city, Kunming, in China. We found the performance of current γ(N2O5) parameterizations showed deviations with the varying aerosol liquid water content (ALWC). Such differences would lead to biased estimation on particulate nitrate production potential. Our findings suggest the directions for future studies.
Mingjie Kang, Mengying Bao, Wenhuai Song, Aduburexiati Abulimiti, Changliu Wu, Fang Cao, Sönke Szidat, and Yanlin Zhang
Atmos. Chem. Phys., 25, 73–91, https://doi.org/10.5194/acp-25-73-2025, https://doi.org/10.5194/acp-25-73-2025, 2025
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Reports on molecular-level knowledge of high-temporal-resolution particulate matter ≤2.5 µm in diameter (PM2.5) on hazy days are limited. We investigated various PM2.5 species and their sources. The results show biomass burning (BB) was the main source of organic carbon. Moreover, BB enhanced fungal spore emissions and secondary aerosol formation. The contribution of non-fossil sources increased with increasing haze pollution, suggesting BB may be an important driver of haze events in winter.
Gregory P. Schill, Karl D. Froyd, Daniel M. Murphy, Christina J. Williamson, Charles A. Brock, Tomás Sherwen, Mat J. Evans, Eric A. Ray, Eric C. Apel, Rebecca S. Hornbrook, Alan J. Hills, Jeff Peischl, Thomas B. Ryerson, Chelsea R. Thompson, Ilann Bourgeois, Donald R. Blake, Joshua P. DiGangi, and Glenn S. Diskin
Atmos. Chem. Phys., 25, 45–71, https://doi.org/10.5194/acp-25-45-2025, https://doi.org/10.5194/acp-25-45-2025, 2025
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Using single-particle mass spectrometry, we show that trace concentrations of bromine and iodine are ubiquitous in remote tropospheric aerosol and suggest that aerosols are an important part of the global reactive iodine budget. Comparisons to a global climate model with detailed iodine chemistry are favorable in the background atmosphere; however, the model cannot replicate our measurements near the ocean surface, in biomass burning plumes, and in the stratosphere.
Yanqin Ren, Zhenhai Wu, Fang Bi, Hong Li, Haijie Zhang, Junling Li, Rui Gao, Fangyun Long, Zhengyang Liu, Yuanyuan Ji, and Gehui Wang
EGUsphere, https://doi.org/10.5194/egusphere-2024-3678, https://doi.org/10.5194/egusphere-2024-3678, 2025
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The daily concentrations of Polycyclic aromatic hydrocarbons (PAHs), oxygenated PAHs (OPAHs), and nitrated phenols (NPs) in PM2.5 were all increased during the heating season. Biomass burning was identified to be the primary source of these aromatic compounds, particularly for PAHs. Phenol and nitrobenzene are two main primary precursors for 4NP, with phenol showing lower reaction barriers. P-Cresol was identified as the primary precursor for the formation of 4-methyl-5-nitrocatechol.
Capucine Camin, François Lacan, Catherine Pradoux, Marie Labatut, Anne Johansen, and James W. Murray
EGUsphere, https://doi.org/10.5194/egusphere-2024-3777, https://doi.org/10.5194/egusphere-2024-3777, 2024
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This manuscript presents the chemical composition of aerosols (> 1µm) over the Equatorial and Tropical Pacific Ocean, presenting the first measurements of iron isotopes in aerosols from this region. Iron concentrations and isotopes were determined using a Neptune MC-ICPMS. Our data analysis reveals that a significant portion of the aerosols undergo dissolution and removal during atmospheric transport. These findings contribute to original conclusions about the chemistry and physics of aerosols.
Andreas Aktypis, Dontavious J. Sippial, Christina N. Vasilakopoulou, Angeliki Matrali, Christos Kaltsonoudis, Andrea Simonati, Marco Paglione, Matteo Rinaldi, Stefano Decesari, and Spyros N. Pandis
Atmos. Chem. Phys., 24, 13769–13791, https://doi.org/10.5194/acp-24-13769-2024, https://doi.org/10.5194/acp-24-13769-2024, 2024
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A dual-chamber system was deployed in two different environments (Po Valley, Italy, and Pertouli forest, Greece) to study the potential of ambient air directly injected into the chambers, to form secondary organic aerosol (SOA). In the Po Valley, the system reacts rapidly, forming large amounts of SOA, while in Pertouli the SOA formation chemistry appears to have been practically terminated before the beginning of most experiments, so there is little additional SOA formation potential left.
Amna Ijaz, Brice Temime-Roussel, Benjamin Chazeau, Sarah Albertin, Stephen R. Arnold, Brice Barrett, Slimane Bekki, Natalie Brett, Meeta Cesler-Maloney, Elsa Dieudonne, Kayane K. Dingilian, Javier G. Fochesatto, Jingqiu Mao, Allison Moon, Joel Savarino, William Simpson, Rodney J. Weber, Kathy S. Law, and Barbara D'Anna
EGUsphere, https://doi.org/10.5194/egusphere-2024-3789, https://doi.org/10.5194/egusphere-2024-3789, 2024
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Fairbanks is among the most polluted cities with the highest particulate matter (PM) levels in the US during winters. Highly time-resolved measurements of the sub-micron PM elucidated residential heating with wood and oil and hydrocarbon-like organics from traffic, as well as sulphur-containing organic aerosol, to be the key pollution sources. Remarkable differences existed between complementary instruments, warranting the deployment of multiple tools at sites with wide-ranging influences.
Fredrik Mattsson, Almuth Neuberger, Liine Heikkinen, Yvette Gramlich, Marco Paglione, Matteo Rinaldi, Stefano Decesari, Paul Zieger, Ilona Riipinen, and Claudia Mohr
EGUsphere, https://doi.org/10.5194/egusphere-2024-3629, https://doi.org/10.5194/egusphere-2024-3629, 2024
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This study investigated aerosol-cloud interactions, focusing on organic nitrogen (ON) formation in the aqueous phase. Measurements were conducted in wintertime Italian Po Valley, using aerosol mass spectrometry. The fog was enriched in more hygroscopic inorganic compounds and ON, containing e.g. imidazoles. The formation of imidazole by aerosol-fog interactions could be confirmed for the first time in atmospheric observations. Findings highlight the role of fog in nitrogen aerosol formation.
Jie Zhang, Tianyu Zhu, Alexandra Catena, Yaowei Li, Margaret J. Schwab, Pengfei Liu, Akua Asa-Awuku, and James Schwab
Atmos. Chem. Phys., 24, 13445–13456, https://doi.org/10.5194/acp-24-13445-2024, https://doi.org/10.5194/acp-24-13445-2024, 2024
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This study shows the derived organic aerosol hygroscopicity under high-humidity conditions based on a simple optical scatter monitor system, including two nephelometric monitors (pDR-1500), when the aerosol chemical composition is already known.
Wei Yuan, Ru-Jin Huang, Chao Luo, Lu Yang, Wenjuan Cao, Jie Guo, and Huinan Yang
Atmos. Chem. Phys., 24, 13219–13230, https://doi.org/10.5194/acp-24-13219-2024, https://doi.org/10.5194/acp-24-13219-2024, 2024
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We characterized water-soluble oxidative potential (OP) levels in wintertime PM2.5 in the south and north of Beijing. Our results show that the volume-normalized dithiothreitol (DTTv) in the north was comparable to that in the south, while the mass-normalized dithiothreitol (DTTm) in the north was almost twice that in the south. Traffic-related emissions and biomass burning were the main sources of DTTv in the south, and traffic-related emissions contributed the most to DTTv in the north.
Mingfu Cai, Chenshuo Ye, Bin Yuan, Shan Huang, E Zheng, Suxia Yang, Zelong Wang, Yi Lin, Tiange Li, Weiwei Hu, Wei Chen, Qicong Song, Wei Li, Yuwen Peng, Baoling Liang, Qibin Sun, Jun Zhao, Duohong Chen, Jiaren Sun, Zhiyong Yang, and Min Shao
Atmos. Chem. Phys., 24, 13065–13079, https://doi.org/10.5194/acp-24-13065-2024, https://doi.org/10.5194/acp-24-13065-2024, 2024
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This study investigated the daytime secondary organic aerosol (SOA) formation in urban plumes. We observed a significant daytime SOA formation through gas–particle partitioning when the site was affected by urban plumes. A box model simulation indicated that urban pollutants (nitrogen oxide and volatile organic compounds) could enhance the oxidizing capacity, while the elevated volatile organic compounds were mainly responsible for promoting daytime SOA formation.
Qingxiao Meng, Yunjiang Zhang, Sheng Zhong, Jie Fang, Lili Tang, Yongcai Rao, Minfeng Zhou, Jian Qiu, Xiaofeng Xu, Jean-Eudes Petit, Olivier Favez, and Xinlei Ge
EGUsphere, https://doi.org/10.5194/egusphere-2024-2776, https://doi.org/10.5194/egusphere-2024-2776, 2024
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We developed a new method to reconstruct missing elemental carbon (EC) data in four Chinese cities from 2013 to 2023. Using machine learning, we accurately filled data gaps and introduced a new approach to analyze EC trends. Our findings reveal a significant decline in EC due to stricter pollution controls, though this slowed after 2020. This study provides a versatile framework for addressing data gaps and supports strategies to reduce urban air pollution and its climate impacts.
Yingjie Shen, Rudra P. Pokhrel, Amy P. Sullivan, Ezra J. T. Levin, Lauren A. Garofalo, Delphine K. Farmer, Wade Permar, Lu Hu, Darin W. Toohey, Teresa Campos, Emily V. Fischer, and Shane M. Murphy
Atmos. Chem. Phys., 24, 12881–12901, https://doi.org/10.5194/acp-24-12881-2024, https://doi.org/10.5194/acp-24-12881-2024, 2024
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The magnitude and evolution of brown carbon (BrC) absorption remain unclear, with uncertainty in climate models. Data from the WE-CAN airborne experiment show that model parameterizations overestimate the mass absorption cross section (MAC) of BrC. Observed decreases in BrC absorption with chemical markers are due to decreasing organic aerosol (OA) mass rather than a decreasing BrC MAC, which is currently implemented in models. Water-soluble BrC contributes 23 % of total absorption at 660 nm.
Qun He, Zhaowen Wang, Houfeng Liu, Pengju Xu, Rongbao Duan, Caihong Xu, Jianmin Chen, and Min Wei
Atmos. Chem. Phys., 24, 12775–12792, https://doi.org/10.5194/acp-24-12775-2024, https://doi.org/10.5194/acp-24-12775-2024, 2024
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Coastal environments provide an ideal setting for investigating the intermixing of terrestrial and marine aerosols. Terrestrial air mass constituted a larger number of microbes from anthropogenic and soil emissions, whereas saprophytic and gut microbes were predominant in marine samples. Mixed air masses indicated a fusion of marine and terrestrial aerosols, characterized by alterations in the ratio of pathogenic and saprophytic microbes when compared to either terrestrial or marine samples.
Rime El Asmar, Zongrun Li, David J. Tanner, Yongtao Hu, Susan O'Neill, L. Gregory Huey, M. Talat Odman, and Rodney J. Weber
Atmos. Chem. Phys., 24, 12749–12773, https://doi.org/10.5194/acp-24-12749-2024, https://doi.org/10.5194/acp-24-12749-2024, 2024
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Prescribed burning is an important method for managing ecosystems and preventing wildfires. However, smoke from prescribed fires can have a significant impact on air quality. Here, using a network of fixed sites and sampling throughout an extended prescribed burning period in 2 different years, we characterize emissions and evolutions of up to 8 h of PM2.5 mass, black carbon (BC), and brown carbon (BrC) in smoke from burning of forested lands in the southeastern USA.
Matthew Boyer, Diego Aliaga, Lauriane L. J. Quéléver, Silvia Bucci, Hélène Angot, Lubna Dada, Benjamin Heutte, Lisa Beck, Marina Duetsch, Andreas Stohl, Ivo Beck, Tiia Laurila, Nina Sarnela, Roseline C. Thakur, Branka Miljevic, Markku Kulmala, Tuukka Petäjä, Mikko Sipilä, Julia Schmale, and Tuija Jokinen
Atmos. Chem. Phys., 24, 12595–12621, https://doi.org/10.5194/acp-24-12595-2024, https://doi.org/10.5194/acp-24-12595-2024, 2024
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We analyze the seasonal cycle and sources of gases that are relevant for the formation of aerosol particles in the central Arctic. Since theses gases can form new particles, they can influence Arctic climate. We show that the sources of these gases are associated with changes in the Arctic environment during the year, especially with respect to sea ice. Therefore, the concentration of these gases will likely change in the future as the Arctic continues to warm.
Binyu Xiao, Fan Zhang, Zeyu Liu, Yan Zhang, Rui Li, Can Wu, Xinyi Wan, Yi Wang, Yubao Chen, Yong Han, Min Cui, Libo Zhang, Yingjun Chen, and Gehui Wang
EGUsphere, https://doi.org/10.5194/egusphere-2024-3433, https://doi.org/10.5194/egusphere-2024-3433, 2024
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Intermediate/semi-volatile organic compounds in both gas and particle phases from ship exhausts are enhanced due to the switch of fuels from low-sulfur to ultra-low-sulfur. The findings indicate that optimization is necessary for the forthcoming global implementation of an ultra-low-sulfur oil policy. Besides, we find that organic diagnostic markers of hopanes, in conjunction with the ratio of octadecanoic to tetradecanoic could be considered as potential tracers for HFO exhausts.
Mutian Ma, Laura-Hélèna Rivellini, Yichen Zong, Markus Kraft, Liya E. Yu, and Alex King Yin Lee
EGUsphere, https://doi.org/10.5194/egusphere-2024-3240, https://doi.org/10.5194/egusphere-2024-3240, 2024
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This work advances our understanding of emission and atmospheric evolution of black carbon (BC) particles in Singapore, a complex urban environment impacted by multiple local and regional combustion sources, based on the improved source apportionment analysis of real-time aerosol mass spectrometry measurement.
Hongyu Zhang, Shenbo Wang, Zhangsen Dong, Xiao Li, and Ruiqin Zhang
EGUsphere, https://doi.org/10.5194/egusphere-2024-2869, https://doi.org/10.5194/egusphere-2024-2869, 2024
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To address this, 12-year observational data in Zhengzhou were investigated and revealed that the resuspension of surrounding soil dust determined the rebound of crustal material concentrations after 2019, further elevating the particle pH. Therefore, the future ammonia reduction policies in North China may not lead to a rapid increase in particle acidity buffering by the crustal materials, but it is necessary to consider synergistic control with dust sources.
Imad El Haddad, Danielle Vienneau, Kaspar R. Daellenbach, Robin Modini, Jay G. Slowik, Abhishek Upadhyay, Petros N. Vasilakos, David Bell, Kees de Hoogh, and Andre S. H. Prevot
Atmos. Chem. Phys., 24, 11981–12011, https://doi.org/10.5194/acp-24-11981-2024, https://doi.org/10.5194/acp-24-11981-2024, 2024
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This opinion paper explores how advances in aerosol science inform our understanding of the health impacts of outdoor particulate pollution. We advocate for a shift in the way we target PM pollution, focusing on the most harmful anthropogenic emissions. We highlight key observations, modelling developments, and emission measurements needed to achieve this shift.
Yu Huang, Xingru Li, Dan Dan Huang, Ruoyuan Lei, Binhuang Zhou, Yunjiang Zhang, and Xinlei Ge
EGUsphere, https://doi.org/10.5194/egusphere-2024-2757, https://doi.org/10.5194/egusphere-2024-2757, 2024
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This work performed a comprehensive investigation on the chemical and optical properties of the brown carbon in PM2.5 samples collected in Nanjing, China. In particular, we used the machine learning approach to identify a list of key BrC species, which can be a good reference for future studies. Our findings extend the understanding on BrC properties and are valuable to the assessment of its impact on air quality and radiative forcing.
Cited articles
Adams, P. J., Seinfeld, J. H., Koch, D., Mickley, L., and Jacob, D.: General
circulation model assessment of direct radiative forcing by the
sulfate-nitrate-ammonium-water inorganic aerosol system, J. Geophys.
Res.-Atmos., 106, 1097–1111, 2001.
Ahlm, L., Shakya, K. M., Russell, L. M., Schroder, J. C., Wong, J. P. S.,
Sjostedt, S. J., Hayden, K. L., Liggio, J., Wentzell, J. J. B., Wiebe, H. A.,
Mihele, C., Leaitch, W. R., and Macdonald, A. M.: Temperature-dependent
accumulation mode particle and cloud nuclei concentrations from biogenic
sources during WACS 2010, Atmos. Chem. Phys., 13, 3393–3407,
https://doi.org/10.5194/acp-13-3393-2013, 2013.
Aiken, A. C., Decarlo, P. F., Kroll, J. H., Worsnop, D. R., Huffman, J. A.,
Docherty, K. S., Ulbrich, I. M., Mohr, C., Kimmel, J. R., Sueper, D., Sun,
Y., Zhang, Q., Trimborn, A., Northway, M., Ziemann, P. J., Canagaratna, M.
R., Onasch, T. B., Alfarra, M. R., Prevot, A. S. H., Dommen, J., Duplissy,
J., Metzger, A., Baltensperger, U., and Jimenez, J. L.: O∕C and
OM∕OC ratios of primary, secondary, and ambient organic aerosols
with high-resolution time-of-flight aerosol mass spectrometry, Environ. Sci.
Technol., 42, 4478–4485, 2008.
Ambrose, J. L., Reidmiller, D. R., and Jaffe, D. A.: Causes of high
O3 in the lower free troposphere over the Pacific Northwest as
observed at the Mt. Bachelor Observatory, Atmos. Environ., 45, 5302–5315,
2011.
Bahreini, R., Jimenez, J. L., Wang, J., Flagan, R. C., Seinfeld, J. H.,
Jayne, J. T., and Worsnop, D. R.: Aircraft-based aerosol size and composition
measurements during ACE-Asia using an Aerodyne aerosol mass spectrometer, J.
Geophys. Res.-Atmos., 108, 8645, https://doi.org/10.1029/2002JD003226, 2003.
Bianchi, F., Trostl, J., Junninen, H., Frege, C., Henne, S., Hoyle, C. R.,
Molteni, U., Herrmann, E., Adamov, A., Bukowiecki, N., Chen, X., Duplissy,
J., Gysel, M., Hutterli, M., Kangasluoma, J., Kontkanen, J., Kurten, A.,
Manninen, H. E., Munch, S., Perakyla, O., Petaja, T., Rondo, L., Williamson,
C., Weingartner, E., Curtius, J., Worsnop, D. R., Kulmala, M., Dommen, J.,
and Baltensperger, U.: New particle formation in the free troposphere: A
question of chemistry and timing, Science, 352, 1109–1112, 2016.
Bolton, D.: The Computation of Equivalent Potential Temperature, Mon.
Weather Rev., 108, 1046–1053, 1980.
Boucher, O., Randall, D., Artaxo, P., Bretherton, C., Feingold, G., Forster,
P., Kerminen, V.-M., Kondo, Y., Liao, H., Lohmann, U., Rasch, P., Satheesh,
S. K., Sherwood, S., Stevens, B., and Zhang, X. Y.: Clouds and Aerosols, in:
Climate Change 2013: The Physical Science Basis, Contribution of Working
Group I to the Fifth Assessment Report of the Intergovernmental Panel on
Climate Change, Cambridge University Press, Cambridge, UK and New York, NY,
USA, 573–575, 2013.
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.
Briggs, N. L., Jaffe, D. A., Gao, H., Hee, J. R., Baylon, P. M., Zhang, Q.,
Zhou, S., Collier, S. C., Sampson, P. D., and Cary, R. A.: Particulate
Matter, Ozone, and Nitrogen Species in Aged Wildfire Plumes Observed at the
Mount Bachelor Observatory, Aerosol Air Qual. Res., 16, 3075–3087, 2016.
Brock, C. A., Cozic, J., Bahreini, R., Froyd, K. D., Middlebrook, A. M.,
McComiskey, A., Brioude, J., Cooper, O. R., Stohl, A., Aikin, K. C., de Gouw,
J. A., Fahey, D. W., Ferrare, R. A., Gao, R.-S., Gore, W., Holloway, J. S.,
Hübler, G., Jefferson, A., Lack, D. A., Lance, S., Moore, R. H., Murphy, D.
M., Nenes, A., Novelli, P. C., Nowak, J. B., Ogren, J. A., Peischl, J.,
Pierce, R. B., Pilewskie, P., Quinn, P. K., Ryerson, T. B., Schmidt, K. S.,
Schwarz, J. P., Sodemann, H., Spackman, J. R., Stark, H., Thomson, D. S.,
Thornberry, T., Veres, P., Watts, L. A., Warneke, C., and Wollny, A. G.:
Characteristics, sources, and transport of aerosols measured in spring 2008
during the aerosol, radiation, and cloud processes affecting Arctic Climate
(ARCPAC) Project, Atmos. Chem. Phys., 11, 2423–2453,
https://doi.org/10.5194/acp-11-2423-2011, 2011.
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, 2015.
Canagaratna, M. R., Jimenez, J. L., Kroll, J. H., Chen, Q., Kessler, S. H.,
Massoli, P., Hildebrandt Ruiz, L., Fortner, E., Williams, L. R., Wilson, K.
R., Surratt, J. D., Donahue, N. M., Jayne, J. T., and Worsnop, D. R.:
Elemental ratio measurements of organic compounds using aerosol mass
spectrometry: characterization, improved calibration, and implications,
Atmos. Chem. Phys., 15, 253–272, https://doi.org/10.5194/acp-15-253-2015,
2015.
Chen, Q., Farmer, D. K., Rizzo, L. V., Pauliquevis, T., Kuwata, M., Karl, T.
G., Guenther, A., Allan, J. D., Coe, H., Andreae, M. O., Pöschl, U.,
Jimenez, J. L., Artaxo, P., and Martin, S. T.: Submicron particle mass
concentrations and sources in the Amazonian wet season (AMAZE-08), Atmos.
Chem. Phys., 15, 3687–3701, https://doi.org/10.5194/acp-15-3687-2015, 2015.
Collier, S. and Zhang, Q.: Gas-Phase CO2 Subtraction for Improved
Measurements of the Organic Aerosol Mass Concentration and Oxidation Degree
by an Aerosol Mass Spectrometer, Environ. Sci. Technol., 47, 14324–14331,
2013.
Collier, S., Zhou, S., Kuwayama, T., Forestieri, S., Brady, J., Zhang, M.,
Kleeman, M., Cappa, C., Bertram, T., and Zhang, Q.: Organic PM Emissions from
Vehicles: Composition, O∕C Ratio, and Dependence on PM
Concentration, Aerosol Sci. Tech., 49, 86–97, 2015.
Collier, S., Zhou, S., Onasch, T. B., Jaffe, D. A., Kleinman, L., Sedlacek,
A. J., Briggs, N. L., Hee, J., Fortner, E., Shilling, J. E., Worsnop, D.,
Yokelson, R. J., Parworth, C., Ge, X., Xu, J., Butterfield, Z., Chand, D.,
Dubey, M. K., Pekour, M. S., Springston, S., and Zhang, Q.: Regional
Influence of Aerosol Emissions from Wildfires Driven by Combustion
Efficiency: Insights from the BBOP Campaign, Environ. Sci. Technol., 50,
8613–8622, 2016.
Cozic, J., Verheggen, B., Weingartner, E., Crosier, J., Bower, K. N., Flynn,
M., Coe, H., Henning, S., Steinbacher, M., Henne, S., Collaud Coen, M.,
Petzold, A., and Baltensperger, U.: Chemical composition of free tropospheric
aerosol for PM1 and coarse mode at the high alpine site Jungfraujoch,
Atmos. Chem. Phys., 8, 407–423, https://doi.org/10.5194/acp-8-407-2008,
2008.
Cubison, M. J., Ortega, A. M., Hayes, P. L., Farmer, D. K., Day, D., Lechner,
M. J., Brune, W. H., Apel, E., Diskin, G. S., Fisher, J. A., Fuelberg, H. E.,
Hecobian, A., Knapp, D. J., Mikoviny, T., Riemer, D., Sachse, G. W.,
Sessions, W., Weber, R. J., Weinheimer, A. J., Wisthaler, A., and Jimenez, J.
L.: Effects of aging on organic aerosol from open biomass burning smoke in
aircraft and laboratory studies, Atmos. Chem. Phys., 11, 12049–12064,
https://doi.org/10.5194/acp-11-12049-2011, 2011.
DeCarlo, P. F., Dunlea, E. J., Kimmel, J. R., Aiken, A. C., Sueper, D.,
Crounse, J., Wennberg, P. O., Emmons, L., Shinozuka, Y., Clarke, A., Zhou,
J., Tomlinson, J., Collins, D. R., Knapp, D., Weinheimer, A. J., Montzka, D.
D., Campos, T., and Jimenez, J. L.: Fast airborne aerosol size and chemistry
measurements above Mexico City and Central Mexico during the MILAGRO
campaign, Atmos. Chem. Phys., 8, 4027–4048,
https://doi.org/10.5194/acp-8-4027-2008, 2008.
Draxler, R. R. and Hess, G. D.: An overview of the Hysplit-4 modeling system
for trajectories, dispersion, and deposition, Aust. Meteorol. Magn., 47,
295–308, 1998.
Dunlea, E. J., DeCarlo, P. F., Aiken, A. C., Kimmel, J. R., Peltier, R. E.,
Weber, R. J., Tomlinson, J., Collins, D. R., Shinozuka, Y., McNaughton, C.
S., Howell, S. G., Clarke, A. D., Emmons, L. K., Apel, E. C., Pfister, G. G.,
van Donkelaar, A., Martin, R. V., Millet, D. B., Heald, C. L., and Jimenez,
J. L.: Evolution of Asian aerosols during transpacific transport in INTEX-B,
Atmos. Chem. Phys., 9, 7257–7287, https://doi.org/10.5194/acp-9-7257-2009,
2009.
Dzepina, K., Mazzoleni, C., Fialho, P., China, S., Zhang, B., Owen, R. C.,
Helmig, D., Hueber, J., Kumar, S., Perlinger, J. A., Kramer, L. J., Dziobak,
M. P., Ampadu, M. T., Olsen, S., Wuebbles, D. J., and Mazzoleni, L. R.:
Molecular characterization of free tropospheric aerosol collected at the Pico
Mountain Observatory: a case study with a long-range transported biomass
burning plume, Atmos. Chem. Phys., 15, 5047–5068,
https://doi.org/10.5194/acp-15-5047-2015, 2015.
Eastwood, M. L., Cremel, S., Wheeler, M., Murray, B. J., Girard, E., and
Bertram, A. K.: Effects of sulfuric acid and ammonium sulfate coatings on the
ice nucleation properties of kaolinite particles, Geophys. Res. Lett., 36,
L02811, https://doi.org/10.1029/2008GL035997, 2009.
Ervens, B., Turpin, B. J., and Weber, R. J.: Secondary organic aerosol
formation in cloud droplets and aqueous particles (aqSOA): a review of
laboratory, field and model studies, Atmos. Chem. Phys., 11, 11069–11102,
https://doi.org/10.5194/acp-11-11069-2011, 2011.
Ervens, B., Wang, Y., Eagar, J., Leaitch, W. R., Macdonald, A. M., Valsaraj,
K. T., and Herckes, P.: Dissolved organic carbon (DOC) and select aldehydes
in cloud and fog water: the role of the aqueous phase in impacting trace gas
budgets, Atmos. Chem. Phys., 13, 5117–5135,
https://doi.org/10.5194/acp-13-5117-2013, 2013.
Farmer, D. K., Matsunaga, A., Docherty, K. S., Surratt, J. D., Seinfeld, J.
H., Ziemann, P. J., and Jimenez, J. L.: Response of an aerosol mass
spectrometer to organonitrates and organosulfates and implications for
atmospheric chemistry, P. Natl. Acad. Sci. USA, 107, 6670–6675, 2010.
Fischer, E. V., Jaffe, D. A., Reidmiller, D. R., and Jaegle, L.:
Meteorological controls on observed peroxyacetyl nitrate at Mount Bachelor
during the spring of 2008, J. Geophys. Res.-Atmos., 115, D03302,
https://doi.org/10.1029/2009JD012776, 2010.
Fischer, E. V., Jaffe, D. A., and Weatherhead, E. C.: Free tropospheric
peroxyacetyl nitrate (PAN) and ozone at Mount Bachelor: potential causes of
variability and timescale for trend detection, Atmos. Chem. Phys., 11,
5641–5654, https://doi.org/10.5194/acp-11-5641-2011, 2011.
Fisher, J. A., Jacob, D. J., Wang, Q., Bahreini, R., Carouge, C. C., Cubison,
M. J., Dibb, J. E., Diehl, T., Jimenez, J. L., Leibensperger, E. M., Lu, Z.,
Meinders, M. B. J., Pye, H. O. T., Quinn, P. K., Sharma, S., Streets, D. G.,
van Donkelaar, A., and Yantosca, R. M.: Sources, distribution, and acidity of
sulfate–ammonium aerosol in the Arctic in winter–spring, Atmos. Environ.,
45, 7301–7318, 2011.
Freney, E., Sellegri, K., Asmi, E., Rose, C., Chauvigne, A., Baray, J. L.,
Colomb, A., Hervo, M., Montoux, N., Bouvier, L., and Picard, D.: Experimental
Evidence of the Feeding of the Free Troposphere with Aerosol Particles from
the Mixing Layer, Aerosol Air Qual. Res., 16, 702–716, 2016.
Fröhlich, R., Cubison, M. J., Slowik, J. G., Bukowiecki, N., Canonaco, F.,
Croteau, P. L., Gysel, M., Henne, S., Herrmann, E., Jayne, J. T.,
Steinbacher, M., Worsnop, D. R., Baltensperger, U., and Prévôt, A. S. H.:
Fourteen months of on-line measurements of the non-refractory submicron
aerosol at the Jungfraujoch (3580 m a.s.l.) – chemical composition,
origins and organic aerosol sources, Atmos. Chem. Phys., 15, 11373–11398,
https://doi.org/10.5194/acp-15-11373-2015, 2015.
Froyd, K. D., Murphy, D. M., Sanford, T. J., Thomson, D. S., Wilson, J. C.,
Pfister, L., and Lait, L.: Aerosol composition of the tropical upper
troposphere, Atmos. Chem. Phys., 9, 4363–4385,
https://doi.org/10.5194/acp-9-4363-2009, 2009.
Fry, J. L., Kiendler-Scharr, A., Rollins, A. W., Wooldridge, P. J., Brown, S.
S., Fuchs, H., Dubé, W., Mensah, A., dal Maso, M., Tillmann, R., Dorn,
H.-P., Brauers, T., and Cohen, R. C.: Organic nitrate and secondary organic
aerosol yield from NO3 oxidation of β-pinene evaluated using a
gas-phase kinetics/aerosol partitioning model, Atmos. Chem. Phys., 9,
1431–1449, https://doi.org/10.5194/acp-9-1431-2009, 2009.
Fry, J. L., Draper, D. C., Zarzana, K. J., Campuzano-Jost, P., Day, D. A.,
Jimenez, J. L., Brown, S. S., Cohen, R. C., Kaser, L., Hansel, A., Cappellin,
L., Karl, T., Hodzic Roux, A., Turnipseed, A., Cantrell, C., Lefer, B. L.,
and Grossberg, N.: Observations of gas- and aerosol-phase organic nitrates at
BEACHON-RoMBAS 2011, Atmos. Chem. Phys., 13, 8585–8605,
https://doi.org/10.5194/acp-13-8585-2013, 2013.
Ge, X. L., Zhang, Q., Sun, Y. L., Ruehl, C. R., and Setyan, A.: Effect of
aqueous-phase processing on aerosol chemistry and size distributions in
Fresno, California, during wintertime, Environ. Chem., 9, 221–235, 2012.
Hallar, A. G., Lowenthal, D. H., Chirokova, G., Borys, R. D., and Wiedinmyer,
C.: Persistent daily new particle formation at a mountain-top location,
Atmos. Environ., 45, 4111–4115, 2011.
Hallar, A. G., Lowenthal, D. H., Clegg, S. L., Samburova, V., Taylor, N.,
Mazzoleni, L. R., Zielinska, B. K., Kristensen, T. B., Chirokova, G.,
McCubbin, I. B., Dodson, C., and Collins, D.: Chemical and hygroscopic
properties of aerosol organics at Storm Peak Laboratory, J. Geophys.
Res.-Atmos., 118, 4767–4779, 2013.
Hallar, A. G., Petersen, R., McCubbin, I. B., Lowenthal, D., Lee, S.,
Andrews, E., and Yu, F.: Climatology of New Particle Formation and
Corresponding Precursors at Storm Peak Laboratory, Aerosol Air Qual. Res.,
16, 816–826, 2016.
Huang, S., Poulain, L., van Pinxteren, D., van Pinxteren, M., Wu, Z.,
Herrmann, H., and Wiedensohler, A.: Latitudinal and Seasonal Distribution of
Particulate MSA over the Atlantic using a Validated Quantification Method
with HR-ToF-AMS, Environ. Sci. Technol., 51, 418–426, 2017.
Jacobson, M. Z.: Global direct radiative forcing due to multicomponent
anthropogenic and natural aerosols, J. Geophys. Res.-Atmos., 106, 1551–1568,
2001.
Jaffe, D., Prestbo, E., Swartzendruber, P., Weiss-Penzias, P., Kato, S.,
Takami, A., Hatakeyama, S., and Kajii, Y.: Export of atmospheric mercury from
Asia, Atmos. Environ., 39, 3029–3038, 2005a.
Jaffe, D., Tamura, S., and Harris, J.: Seasonal cycle and composition of
background fine particles along the west coast of the US, Atmos. Environ.,
39, 297–306, 2005b.
Johnson, S. A. and Kumar, R.: Composition and spectral characteristics of
ambient aerosol at Mauna Loa Observatory, J. Geophys. Res.-Atmos., 96,
5379–5386, 1991.
Kiendler-Scharr, A., Mensah, A. A., Friese, E., Topping, D., Nemitz, E.,
Prevot, A. S. H., Aijala, M., Allan, J., Canonaco, F., Canagaratna, M.,
Carbone, S., Crippa, M., Dall Osto, M., Day, D. A., De Carlo, P., Di Marco,
C. F., Elbern, H., Eriksson, A., Freney, E., Hao, L., Herrmann, H.,
Hildebrandt, L., Hillamo, R., Jimenez, J. L., Laaksonen, A., McFiggans, G.,
Mohr, C., O'Dowd, C., Otjes, R., Ovadnevaite, J., Pandis, S. N., Poulain, L.,
Schlag, P., Sellegri, K., Swietlicki, E., Tiitta, P., Vermeulen, A., Wahner,
A., Worsnop, D., and Wu, H. C.: Ubiquity of organic nitrates from nighttime
chemistry in the European submicron aerosol, Geophys. Res. Lett., 43,
7735–7744, 2016.
Kiendler-Scharr, A., Zhang, Q., Hohaus, T., Kleist, E., Mensah, A., Mentel,
T. F., Spindler, C., Uerlings, R., Tillmann, R., and Wildt, J.: Aerosol Mass
Spectrometric Features of Biogenic SOA: Observations from a Plant Chamber and
in Rural Atmospheric Environments, Environ. Sci. Technol., 43, 8166–8172,
2009.
Kim, H., Collier, S., Ge, X., Xu, J., Sun, Y., Jiang, W., Wang, Y., Herckes,
P., and Zhang, Q.: Chemical processing of water-soluble species and formation
of secondary organic aerosol in fogs, Atmos. Environ., 200, 158–166, 2019.
Koop, T., Luo, B., Tsias, A., and Peter, T.: Water activity as the
determinant for homogeneous ice nucleation in aqueous solutions, Nature, 406,
611–614, 2000.
Kroll, J. H., Donahue, N. M., Jimenez, J. L., Kessler, S. H., Canagaratna, M.
R., Wilson, K. R., Altieri, K. E., Mazzoleni, L. R., Wozniak, A. S., Bluhm,
H., Mysak, E. R., Smith, J. D., Kolb, C. E., and Worsnop, D. R.: Carbon
oxidation state as a metric for describing the chemistry of atmospheric
organic aerosol, Nat. Chem., 3, 133–139, 2011.
Laing, J. R., Jaffe, D. A., and Hee, J. R.: Physical and optical properties
of aged biomass burning aerosol from wildfires in Siberia and the Western USA
at the Mt. Bachelor Observatory, Atmos. Chem. Phys., 16, 15185–15197,
https://doi.org/10.5194/acp-16-15185-2016, 2016.
Lee, A., Goldstein, A. H., Keywood, M. D., Gao, S., Varutbangkul, V.,
Bahreini, R., Ng, N. L., Flagan, R. C., and Seinfeld, J. H.: Gas-phase
products and secondary aerosol yields from the ozonolysis of ten different
terpenes, J. Geophys. Res.-Atmos., 111, D07302, https://doi.org/10.1029/2005JD006437,
2006.
Lee, A. K. Y., Herckes, P., Leaitch, W. R., Macdonald, A. M., and Abbatt, J.
P. D.: Aqueous OH oxidation of ambient organic aerosol and cloud water
organics: Formation of highly oxidized products, Geophys. Res. Lett., 38,
L11805, https://doi.org/10.1029/2011GL047439, 2011.
Lee, A. K. Y., Hayden, K. L., Herckes, P., Leaitch, W. R., Liggio, J.,
Macdonald, A. M., and Abbatt, J. P. D.: Characterization of aerosol and cloud
water at a mountain site during WACS 2010: secondary organic aerosol
formation through oxidative cloud processing, Atmos. Chem. Phys., 12,
7103–7116, https://doi.org/10.5194/acp-12-7103-2012, 2012.
Lee, A. K. Y., Abbatt, J. P. D., Leaitch, W. R., Li, S.-M., Sjostedt, S. J.,
Wentzell, J. J. B., Liggio, J., and Macdonald, A. M.: Substantial secondary
organic aerosol formation in a coniferous forest: observations of both day-
and nighttime chemistry, Atmos. Chem. Phys., 16, 6721–6733,
https://doi.org/10.5194/acp-16-6721-2016, 2016.
McClure, C. D., Jaffe, D. A., and Gao, H.: Carbon Dioxide in the Free
Troposphere and Boundary Layer at the Mt. Bachelor Observatory, Aerosol Air
Qual. Res., 16, 717–728, 2016.
Middlebrook, A. M., Bahreini, R., Jimenez, J. L., and Canagaratna, M. R.:
Evaluation of Composition-Dependent Collection Efficiencies for the Aerodyne
Aerosol Mass Spectrometer using Field Data, Aerosol Sci. Tech., 46, 258–271,
2012.
Ng, N. L., Brown, S. S., Archibald, A. T., Atlas, E., Cohen, R. C., Crowley,
J. N., Day, D. A., Donahue, N. M., Fry, J. L., Fuchs, H., Griffin, R. J.,
Guzman, M. I., Herrmann, H., Hodzic, A., Iinuma, Y., Jimenez, J. L.,
Kiendler-Scharr, A., Lee, B. H., Luecken, D. J., Mao, J., McLaren, R.,
Mutzel, A., Osthoff, H. D., Ouyang, B., Picquet-Varrault, B., Platt, U., Pye,
H. O. T., Rudich, Y., Schwantes, R. H., Shiraiwa, M., Stutz, J., Thornton, J.
A., Tilgner, A., Williams, B. J., and Zaveri, R. A.: Nitrate radicals and
biogenic volatile organic compounds: oxidation, mechanisms, and organic
aerosol, Atmos. Chem. Phys., 17, 2103–2162,
https://doi.org/10.5194/acp-17-2103-2017, 2017.
Ng, N. L., Canagaratna, M. R., Zhang, Q., Jimenez, J. L., Tian, J., Ulbrich,
I. M., Kroll, J. H., Docherty, K. S., Chhabra, P. S., Bahreini, R., Murphy,
S. M., Seinfeld, J. H., Hildebrandt, L., Donahue, N. M., DeCarlo, P. F.,
Lanz, V. A., Prévôt, A. S. H., Dinar, E., Rudich, Y., and Worsnop, D. R.:
Organic aerosol components observed in Northern Hemispheric datasets from
Aerosol Mass Spectrometry, Atmos. Chem. Phys., 10, 4625–4641,
https://doi.org/10.5194/acp-10-4625-2010, 2010.
Paatero, P. and Tapper, U.: Positive Matrix Factorization – a Nonnegative
Factor Model with Optimal Utilization of Error-Estimates of Data Values,
Environmetrics, 5, 111–126, 1994.
Phinney, L., Richard Leaitch, W., Lohmann, U., Boudries, H., Worsnop, D. R.,
Jayne, J. T., Toom-Sauntry, D., Wadleigh, M., Sharma, S., and Shantz, N.:
Characterization of the aerosol over the sub-arctic north east Pacific Ocean,
Deep Sea Res., 53, 2410–2433, 2006.
Reidmiller, D. R., Jaffe, D. A., Fischer, E. V., and Finley, B.: Nitrogen
oxides in the boundary layer and free troposphere at the Mt. Bachelor
Observatory, Atmos. Chem. Phys., 10, 6043–6062,
https://doi.org/10.5194/acp-10-6043-2010, 2010.
Rinaldi, M., Gilardoni, S., Paglione, M., Sandrini, S., Fuzzi, S., Massoli,
P., Bonasoni, P., Cristofanelli, P., Marinoni, A., Poluzzi, V., and Decesari,
S.: Organic aerosol evolution and transport observed at Mt. Cimone
(2165 m a.s.l.), Italy, during the PEGASOS campaign, Atmos. Chem. Phys.,
15, 11327–11340, https://doi.org/10.5194/acp-15-11327-2015, 2015.
Ripoll, A., Minguillón, M. C., Pey, J., Jimenez, J. L., Day, D. A.,
Sosedova, Y., Canonaco, F., Prévôt, A. S. H., Querol, X., and Alastuey,
A.: Long-term real-time chemical characterization of submicron aerosols at
Montsec (southern Pyrenees, 1570 m a.s.l.), Atmos. Chem. Phys., 15,
2935–2951, https://doi.org/10.5194/acp-15-2935-2015, 2015.
Roberts, G. C., Day, D. A., Russell, L. M., Dunlea, E. J., Jimenez, J. L.,
Tomlinson, J. M., Collins, D. R., Shinozuka, Y., and Clarke, A. D.:
Characterization of particle cloud droplet activity and composition in the
free troposphere and the boundary layer during INTEX-B, Atmos. Chem. Phys.,
10, 6627–6644, https://doi.org/10.5194/acp-10-6627-2010, 2010.
Robinson, N. H., Hamilton, J. F., Allan, J. D., Langford, B., Oram, D. E.,
Chen, Q., Docherty, K., Farmer, D. K., Jimenez, J. L., Ward, M. W., Hewitt,
C. N., Barley, M. H., Jenkin, M. E., Rickard, A. R., Martin, S. T.,
McFiggans, G., and Coe, H.: Evidence for a significant proportion of
Secondary Organic Aerosol from isoprene above a maritime tropical forest,
Atmos. Chem. Phys., 11, 1039–1050, https://doi.org/10.5194/acp-11-1039-2011,
2011.
Rose, C., Sellegri, K., Asmi, E., Hervo, M., Freney, E., Colomb, A.,
Junninen, H., Duplissy, J., Sipilä, M., Kontkanen, J., Lehtipalo, K., and
Kulmala, M.: Major contribution of neutral clusters to new particle formation
at the interface between the boundary layer and the free troposphere, Atmos.
Chem. Phys., 15, 3413–3428, https://doi.org/10.5194/acp-15-3413-2015, 2015.
Schroder, F., Karcher, B., Fiebig, M., and Petzold, A.: Aerosol states in the
free troposphere at northern midlatitudes, J. Geophys. Res.-Atmos., 107,
8126–8133, 2002.
Schurman, M. I., Lee, T., Sun, Y., Schichtel, B. A., Kreidenweis, S. M., and
Collett Jr., J. L.: Investigating types and sources of organic aerosol in
Rocky Mountain National Park using aerosol mass spectrometry, Atmos. Chem.
Phys., 15, 737–752, https://doi.org/10.5194/acp-15-737-2015, 2015.
Setyan, A., Zhang, Q., Merkel, M., Knighton, W. B., Sun, Y., Song, C.,
Shilling, J. E., Onasch, T. B., Herndon, S. C., Worsnop, D. R., Fast, J. D.,
Zaveri, R. A., Berg, L. K., Wiedensohler, A., Flowers, B. A., Dubey, M. K.,
and Subramanian, R.: Characterization of submicron particles influenced by
mixed biogenic and anthropogenic emissions using high-resolution aerosol mass
spectrometry: results from CARES, Atmos. Chem. Phys., 12, 8131–8156,
https://doi.org/10.5194/acp-12-8131-2012, 2012.
Sorooshian, A., Crosbie, E., Maudlin, L. C., Youn, J.-S., Wang, Z., Shingler,
T., Ortega, A. M., Hersey, S., and Woods, R. K.: Surface and airborne
measurements of organosulfur and methanesulfonate over the western United
States and coastal areas, J. Geophys. Res.-Atmos., 120, 8535–8548, 2015.
Stohl, A., Trainer, M., Ryerson, T. B., Holloway, J. S., and Parrish, D. D.:
Export of NOy from the North American boundary layer during 1996 and 1997
North Atlantic Regional Experiments, J. Geophys. Res.-Atmos., 107,
4131–4139, 2002.
Sun, Y., Zhang, Q., Macdonald, A. M., Hayden, K., Li, S. M., Liggio, J., Liu,
P. S. K., Anlauf, K. G., Leaitch, W. R., Steffen, A., Cubison, M., Worsnop,
D. R., van Donkelaar, A., and Martin, R. V.: Size-resolved aerosol chemistry
on Whistler Mountain, Canada with a high-resolution aerosol mass spectrometer
during INTEX-B, Atmos. Chem. Phys., 9, 3095–3111,
https://doi.org/10.5194/acp-9-3095-2009, 2009.
Sun, Y. L., Zhang, Q., Schwab, J. J., Yang, T., Ng, N. L., and Demerjian, K.
L.: Factor analysis of combined organic and inorganic aerosol mass spectra
from high resolution aerosol mass spectrometer measurements, Atmos. Chem.
Phys., 12, 8537–8551, https://doi.org/10.5194/acp-12-8537-2012, 2012.
Takahama, S., Schwartz, R. E., Russell, L. M., Macdonald, A. M., Sharma, S.,
and Leaitch, W. R.: Organic functional groups in aerosol particles from
burning and non-burning forest emissions at a high-elevation mountain site,
Atmos. Chem. Phys., 11, 6367–6386, https://doi.org/10.5194/acp-11-6367-2011,
2011.
Timonen, H., Wigder, N., and Jaffe, D.: Influence of background particulate
matter (PM) on urban air quality in the Pacific Northwest, J. Environ.
Manage., 129, 333–340, 2013.
Timonen, H., Jaffe, D. A., Wigder, N., Hee, J., Gao, H., Pitzman, L., and
Cary, R. A.: Sources of carbonaceous aerosol in the free troposphere, Atmos.
Environ., 92, 146–153, 2014.
Tröstl, J., Herrmann, E., Frege, C., Bianchi, F., Molteni, U.,
Bukowiecki, N., Hoyle, C. R., Steinbacher, M., Weingartner, E., Dommen, J.,
Gysel, M., and Baltensperger, U.: Contribution of new particle formation to
the total aerosol concentration at the high-altitude site Jungfraujoch
(3580 m a.s.l., Switzerland), J. Geophys. Res.-Atmos., 121, 11692–11711,
2016.
Ulbrich, I. M., Canagaratna, M. R., Zhang, Q., Worsnop, D. R., and Jimenez,
J. L.: Interpretation of organic components from Positive Matrix
Factorization of aerosol mass spectrometric data, Atmos. Chem. Phys., 9,
2891–2918, https://doi.org/10.5194/acp-9-2891-2009, 2009.
Van Dingenen, R., Putaud, J.-P., Martins-Dos Santos, S., and Raes, F.:
Physical aerosol properties and their relation to air mass origin at Monte
Cimone (Italy) during the first MINATROC campaign, Atmos. Chem. Phys., 5,
2203–2226, https://doi.org/10.5194/acp-5-2203-2005, 2005.
Wagner, N. L., Brock, C. A., Angevine, W. M., Beyersdorf, A., Campuzano-Jost,
P., Day, D., de Gouw, J. A., Diskin, G. S., Gordon, T. D., Graus, M. G.,
Holloway, J. S., Huey, G., Jimenez, J. L., Lack, D. A., Liao, J., Liu, X.,
Markovic, M. Z., Middlebrook, A. M., Mikoviny, T., Peischl, J., Perring, A.
E., Richardson, M. S., Ryerson, T. B., Schwarz, J. P., Warneke, C., Welti,
A., Wisthaler, A., Ziemba, L. D., and Murphy, D. M.: In situ vertical
profiles of aerosol extinction, mass, and composition over the southeast
United States during SENEX and SEAC4RS: observations of a modest aerosol
enhancement aloft, Atmos. Chem. Phys., 15, 7085–7102,
https://doi.org/10.5194/acp-15-7085-2015, 2015.
Wang, J., Krejci, R., Giangrande, S., Kuang, C., Barbosa, H. M., Brito, J.,
Carbone, S., Chi, X., Comstock, J., Ditas, F., Lavric, J., Manninen, H. E.,
Mei, F., Moran-Zuloaga, D., Pohlker, C., Pohlker, M. L., Saturno, J., Schmid,
B., Souza, R. A., Springston, S. R., Tomlinson, J. M., Toto, T., Walter, D.,
Wimmer, D., Smith, J. N., Kulmala, M., Machado, L. A., Artaxo, P., Andreae,
M. O., Petaja, T., and Martin, S. T.: Amazon boundary layer aerosol
concentration sustained by vertical transport during rainfall, Nature, 539,
416–419, 2016.
Watts, S. F.: The mass budgets of carbonyl sulfide, dimethyl sulfide, carbon
disulfide and hydrogen sulfide, Atmos. Environ., 34, 761–779, 2000.
Weiss-Penzias, P., Jaffe, D. A., Swartzendruber, P., Dennison, J. B., Chand,
D., Hafner, W., and Prestbo, E.: Observations of Asian air pollution in the
free troposphere at Mount Bachelor Observatory during the spring of 2004, J.
Geophys. Res.-Atmos., 111, D10304, https://doi.org/10.1029/2005JD006522, 2006.
Worton, D. R., Goldstein, A. H., Farmer, D. K., Docherty, K. S., Jimenez, J.
L., Gilman, J. B., Kuster, W. C., de Gouw, J., Williams, B. J., Kreisberg, N.
M., Hering, S. V., Bench, G., McKay, M., Kristensen, K., Glasius, M.,
Surratt, J. D., and Seinfeld, J. H.: Origins and composition of fine
atmospheric carbonaceous aerosol in the Sierra Nevada Mountains, California,
Atmos. Chem. Phys., 11, 10219–10241,
https://doi.org/10.5194/acp-11-10219-2011, 2011.
Xu, J., Zhang, Q., Shi, J., Ge, X., Xie, C., Wang, J., Kang, S., Zhang, R.,
and Wang, Y.: Chemical characteristics of submicron particles at the central
Tibetan Plateau: insights from aerosol mass spectrometry, Atmos. Chem. Phys.,
18, 427–443, https://doi.org/10.5194/acp-18-427-2018, 2018.
Young, D. E., Kim, H., Parworth, C., Zhou, S., Zhang, X., Cappa, C. D., Seco,
R., Kim, S., and Zhang, Q.: Influences of emission sources and meteorology on
aerosol chemistry in a polluted urban environment: results from DISCOVER-AQ
California, Atmos. Chem. Phys., 16, 5427–5451,
https://doi.org/10.5194/acp-16-5427-2016, 2016.
Zhang, L. and Jaffe, D. A.: Trends and sources of ozone and sub-micron
aerosols at the Mt. Bachelor Observatory (MBO) during 2004–2015, Atmos.
Environ., 165, 143–154, 2017.
Zhang, Q., Jimenez, J. L., Canagaratna, M. R., Allan, J. D., Coe, H.,
Ulbrich, I., Alfarra, M. R., Takami, A., Middlebrook, A. M., Sun, Y. L.,
Dzepina, K., Dunlea, E., Docherty, K., DeCarlo, P. F., Salcedo, D., Onasch,
T., Jayne, J. T., Miyoshi, T., Shimono, A., Hatakeyama, S., Takegawa, N.,
Kondo, Y., Schneider, J., Drewnick, F., Borrmann, S., Weimer, S., Demerjian,
K., Williams, P., Bower, K., Bahreini, R., Cottrell, L., Griffin, R. J.,
Rautiainen, J., Sun, J. Y., Zhang, Y. M., and Worsnop, D. R.: Ubiquity and
dominance of oxygenated species in organic aerosols in
anthropogenically-influenced Northern Hemisphere midlatitudes, Geophys. Res.
Lett., 34, L13801, https://doi.org/10.1029/2007GL029979, 2007.
Zhang, Q., Jimenez, J. L., Canagaratna, M. R., Ulbrich, I. M., Ng, N. L.,
Worsnop, D. R., and Sun, Y. L.: Understanding atmospheric organic aerosols
via factor analysis of aerosol mass spectrometry: a review, Anal. Bioanal.
Chem., 401, 3045–3067, 2011.
Zhang, Q., Zhou, S., Collier, S., Jaffe, D., Onasch, T., Shilling, J.,
Kleinman, L., and Sedlacek, A.: Understanding Composition, Formation, and
Aging of Organic Aerosols in Wildfire Emissions via Combined Mountain Top and
Airborne Measurements. In Multiphase Environmental Chemistry in the
Atmosphere, Am. Chem. Soc., 1299, 363–385, 2018.
Zhou, S., Collier, S., Jaffe, D. A., Briggs, N. L., Hee, J., Sedlacek III, A.
J., Kleinman, L., Onasch, T. B., and Zhang, Q.: Regional influence of
wildfires on aerosol chemistry in the western US and insights into
atmospheric aging of biomass burning organic aerosol, Atmos. Chem. Phys., 17,
2477–2493, https://doi.org/10.5194/acp-17-2477-2017, 2017.
Zhou, S., Collier, S., Xu, J., Mei, F., Wang, J., Lee, Y.-N., Sedlacek, A.
J., Springston, S. R., Sun, Y., and Zhang, Q.: Influences of upwind emission
sources and atmospheric processing on aerosol chemistry and properties at a
rural location in the Northeastern U.S., J. Geophys. Res.-Atmos., 121,
6049–6065, 2016.
Zhu, Q., He, L.-Y., Huang, X.-F., Cao, L.-M., Gong, Z.-H., Wang, C., Zhuang,
X., and Hu, M.: Atmospheric aerosol compositions and sources at two national
background sites in northern and southern China, Atmos. Chem. Phys., 16,
10283–10297, https://doi.org/10.5194/acp-16-10283-2016, 2016.
Zorn, S. R., Drewnick, F., Schott, M., Hoffmann, T., and Borrmann, S.:
Characterization of the South Atlantic marine boundary layer aerosol using an
aerodyne aerosol mass spectrometer, Atmos. Chem. Phys., 8, 4711–4728,
https://doi.org/10.5194/acp-8-4711-2008, 2008.
Short summary
Regional background aerosols in the western US were studied from a mountaintop observatory during summer. Oxygenated organics and sulfate were dominant aerosol components. However, free tropospheric aerosols were more enriched in sulfate, frequently acidic, and comprised mainly of highly oxidized low-volatility organic species. In contrast, organic aerosols in the boundary-layer-influenced air masses were less oxidized and appeared to be semivolatile.
Regional background aerosols in the western US were studied from a mountaintop observatory...
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