Articles | Volume 16, issue 10
https://doi.org/10.5194/acp-16-6577-2016
© Author(s) 2016. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
https://doi.org/10.5194/acp-16-6577-2016
© Author(s) 2016. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Research article
| 
31 May 2016
Research article |
| 31 May 2016
Size-resolved morphological properties of the high Arctic summer aerosol during ASCOS-2008
Evelyne Hamacher-Barth
CORRESPONDING AUTHOR
Department of Meteorology, Stockholm University, 10691 Stockholm,
Sweden
Caroline Leck
Department of Meteorology, Stockholm University, 10691 Stockholm,
Sweden
Kjell Jansson
Department of Materials and Environmental Chemistry, Stockholm
University, 10691 Stockholm, Sweden
Related authors
E. Hamacher-Barth, K. Jansson, and C. Leck
Atmos. Meas. Tech., 6, 3459–3475, https://doi.org/10.5194/amt-6-3459-2013, https://doi.org/10.5194/amt-6-3459-2013, 2013
Caroline Leck, Jost Heintzenberg, Tiina Nygård, and Tuomas Naakka
EGUsphere, https://doi.org/10.5194/egusphere-2025-695, https://doi.org/10.5194/egusphere-2025-695, 2025
Short summary
Short summary
Five summer cruises of the Swedish icebreaker Oden in the inner Arctic in 1990, 1996, 2001, 2008, and 2018 provided a unique dataset on the seasonal distribution of atmospheric aerosol. Coupling these data with the seasonal sea ice distribution strongly indicated a regional biogenic aerosol source during late summer and early autumn freeze-up conditions. Given the expected further warming of the Arctic, we hypothesize an increase in biogenic aerosol in late summer and autumn.
Ines Bulatovic, Julien Savre, Michael Tjernström, Caroline Leck, and Annica M. L. Ekman
Atmos. Chem. Phys., 23, 7033–7055, https://doi.org/10.5194/acp-23-7033-2023, https://doi.org/10.5194/acp-23-7033-2023, 2023
Short summary
Short summary
We use numerical modeling with detailed cloud microphysics to investigate a low-altitude cloud system consisting of two cloud layers – a type of cloud situation which was commonly observed during the summer of 2018 in the central Arctic (north of 80° N). The model generally reproduces the observed cloud layers and the thermodynamic structure of the lower atmosphere well. The cloud system is maintained unless there are low aerosol number concentrations or high large-scale wind speeds.
Ines Bulatovic, Adele L. Igel, Caroline Leck, Jost Heintzenberg, Ilona Riipinen, and Annica M. L. Ekman
Atmos. Chem. Phys., 21, 3871–3897, https://doi.org/10.5194/acp-21-3871-2021, https://doi.org/10.5194/acp-21-3871-2021, 2021
Short summary
Short summary
We use detailed numerical modelling to show that small aerosol particles (diameters ~25–80 nm; so-called Aitken mode particles) significantly influence low-level cloud properties in the clean summertime high Arctic. The small particles can help sustain clouds when the concentration of larger particles is low (<10–20 cm-3). Measurements from four different observational campaigns in the high Arctic support the modelling results as they indicate that Aitken mode aerosols are frequently activated.
André Welti, E. Keith Bigg, Paul J. DeMott, Xianda Gong, Markus Hartmann, Mike Harvey, Silvia Henning, Paul Herenz, Thomas C. J. Hill, Blake Hornblow, Caroline Leck, Mareike Löffler, Christina S. McCluskey, Anne Marie Rauker, Julia Schmale, Christian Tatzelt, Manuela van Pinxteren, and Frank Stratmann
Atmos. Chem. Phys., 20, 15191–15206, https://doi.org/10.5194/acp-20-15191-2020, https://doi.org/10.5194/acp-20-15191-2020, 2020
Short summary
Short summary
Ship-based measurements of maritime ice nuclei concentrations encompassing all oceans are compiled. From this overview it is found that maritime ice nuclei concentrations are typically 10–100 times lower than over continents, while concentrations are surprisingly similar in different oceanic regions. The analysis of the influence of ship emissions shows no effect on the data, making ship-based measurements an efficient strategy for the large-scale exploration of ice nuclei concentrations.
Luisa Ickes, Grace C. E. Porter, Robert Wagner, Michael P. Adams, Sascha Bierbauer, Allan K. Bertram, Merete Bilde, Sigurd Christiansen, Annica M. L. Ekman, Elena Gorokhova, Kristina Höhler, Alexei A. Kiselev, Caroline Leck, Ottmar Möhler, Benjamin J. Murray, Thea Schiebel, Romy Ullrich, and Matthew E. Salter
Atmos. Chem. Phys., 20, 11089–11117, https://doi.org/10.5194/acp-20-11089-2020, https://doi.org/10.5194/acp-20-11089-2020, 2020
Short summary
Short summary
The Arctic is a region where aerosols are scarce. Sea spray might be a potential source of aerosols acting as ice-nucleating particles. We investigate two common phytoplankton species (Melosira arctica and Skeletonema marinoi) and present their ice nucleation activity in comparison with Arctic seawater microlayer samples from different field campaigns. We also aim to understand the aerosolization process of marine biological samples and the potential effect on the ice nucleation activity.
Jost Heintzenberg, Peter Tunved, Martí Galí, and Caroline Leck
Atmos. Chem. Phys., 17, 6153–6175, https://doi.org/10.5194/acp-17-6153-2017, https://doi.org/10.5194/acp-17-6153-2017, 2017
Short summary
Short summary
Events of new particle formation (NPF) were analyzed objectively in a 10-year data set of hourly particle size distributions recorded on Mt. Zeppelin, Spitsbergen, Svalbard. Three different types of NPF events were identified that were hypothesized to be different expressions of related source processes. Back trajectories and ancillary atmospheric and marine data strongly point to marine biogenic sources causing new particle formation in the summer Arctic.
J. Heintzenberg, C. Leck, and P. Tunved
Atmos. Chem. Phys., 15, 6487–6502, https://doi.org/10.5194/acp-15-6487-2015, https://doi.org/10.5194/acp-15-6487-2015, 2015
Short summary
Short summary
Particle size distributions from four summer cruises of the Swedish icebreaker Oden were combined with back trajectories and pack ice information in a cluster algorithm to investigate source areas and aerosol formation in the central Arctic. Five source regions and three aerosol types resulted. Long travel times over ice, combined with more open water conditions shortly before air mass arrival, seem to control the formation of ultrafine particles over the central Arctic pack ice.
C. Leck and E. Svensson
Atmos. Chem. Phys., 15, 2545–2568, https://doi.org/10.5194/acp-15-2545-2015, https://doi.org/10.5194/acp-15-2545-2015, 2015
Short summary
Short summary
In the Arctic clouds are very important for determining the melting of the sea ice. The radiative properties of the optically thin Arctic clouds strongly depend on the number of particles available for water uptake. This study argues that the Köhler equation commonly used for simulating cloud droplet activation is not fully complete for describing the condensational growth of the interaction of the hydrophilic and hydrophobic entities on the structures of the airborne polymer gels present.
J. Browse, K. S. Carslaw, G. W. Mann, C. E. Birch, S. R. Arnold, and C. Leck
Atmos. Chem. Phys., 14, 7543–7557, https://doi.org/10.5194/acp-14-7543-2014, https://doi.org/10.5194/acp-14-7543-2014, 2014
B. Sierau, R. Y.-W. Chang, C. Leck, J. Paatero, and U. Lohmann
Atmos. Chem. Phys., 14, 7409–7430, https://doi.org/10.5194/acp-14-7409-2014, https://doi.org/10.5194/acp-14-7409-2014, 2014
M. Tjernström, C. Leck, C. E. Birch, J. W. Bottenheim, B. J. Brooks, I. M. Brooks, L. Bäcklin, R. Y.-W. Chang, G. de Leeuw, L. Di Liberto, S. de la Rosa, E. Granath, M. Graus, A. Hansel, J. Heintzenberg, A. Held, A. Hind, P. Johnston, J. Knulst, M. Martin, P. A. Matrai, T. Mauritsen, M. Müller, S. J. Norris, M. V. Orellana, D. A. Orsini, J. Paatero, P. O. G. Persson, Q. Gao, C. Rauschenberg, Z. Ristovski, J. Sedlar, M. D. Shupe, B. Sierau, A. Sirevaag, S. Sjogren, O. Stetzer, E. Swietlicki, M. Szczodrak, P. Vaattovaara, N. Wahlberg, M. Westberg, and C. R. Wheeler
Atmos. Chem. Phys., 14, 2823–2869, https://doi.org/10.5194/acp-14-2823-2014, https://doi.org/10.5194/acp-14-2823-2014, 2014
C. Leck, Q. Gao, F. Mashayekhy Rad, and U. Nilsson
Atmos. Chem. Phys., 13, 12573–12588, https://doi.org/10.5194/acp-13-12573-2013, https://doi.org/10.5194/acp-13-12573-2013, 2013
P. Kupiszewski, C. Leck, M. Tjernström, S. Sjogren, J. Sedlar, M. Graus, M. Müller, B. Brooks, E. Swietlicki, S. Norris, and A. Hansel
Atmos. Chem. Phys., 13, 12405–12431, https://doi.org/10.5194/acp-13-12405-2013, https://doi.org/10.5194/acp-13-12405-2013, 2013
E. Hamacher-Barth, K. Jansson, and C. Leck
Atmos. Meas. Tech., 6, 3459–3475, https://doi.org/10.5194/amt-6-3459-2013, https://doi.org/10.5194/amt-6-3459-2013, 2013
M. D. Shupe, P. O. G. Persson, I. M. Brooks, M. Tjernström, J. Sedlar, T. Mauritsen, S. Sjogren, and C. Leck
Atmos. Chem. Phys., 13, 9379–9399, https://doi.org/10.5194/acp-13-9379-2013, https://doi.org/10.5194/acp-13-9379-2013, 2013
Related subject area
Subject: Aerosols | Research Activity: Field Measurements | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Technical note: Towards a stronger observational support for haze pollution control by interpreting carbonaceous aerosol results derived from different measurement approaches
Particle flux–gradient relationships in the high Arctic: emission and deposition patterns across three surface types
Advances in characterization of black carbon particles and their associated coatings using the soot-particle aerosol mass spectrometer in Singapore, a complex city environment
Iron isotopes suggest significant aerosol dissolution over the Pacific Ocean
Enrichment of organic nitrogen in fog residuals observed in the Italian Po Valley
Asian dust transport of proteinaceous matter from the Gobi Desert to northern China
Machine-learning-assisted chemical characterization and optical properties of atmospheric brown carbon in Nanjing, China
Technical note: Reconstructing missing surface aerosol elemental carbon data in long-term series with ensemble learning
Enhanced emission of intermediate-volatility/semi-volatile organic matter in gas and particle phases from ship exhausts with low-sulfur fuels
Measurement report: Crustal materials play an increasing role in elevating particle pH – insights from 12-year records in a typical inland city of China
Significant contributions of biomass burning to PM2.5-bound aromatic compounds: insights from field observations and quantum chemical calculations
Measurement report: In-depth characterization of ship emissions during operations in a Mediterranean port
Direct measurement of N2O5 heterogeneous uptake coefficients on atmospheric aerosols in southwestern China and evaluation of current parameterizations
Measurement report: Per- and polyfluoroalkyl substances (PFAS) in particulate matter (PM10) from activated sludge aeration
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
Long–term Trends in PM2.5 Chemical Composition and Its Impact on Aerosol Properties: Field Observations from 2007 to 2020 in Pearl River Delta, South China
Individual particle compositions and aerosol mixing states at different altitudes over the ocean in East Asia
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
The impacts of pollution sources and temperature on the light absorption of HULIS were revealed by UHPLC-HRMS/MS at the molecular structure level
Effects of Anthropogenic Pollutants on Biogenic Secondary Organic Aerosol Formation in the Atmosphere of Mt. Hua, China
Marine organic aerosol at Mace Head: effects from phytoplankton and source region variability
Elemental composition, iron mineralogy and solubility of anthropogenic and natural mineral dust aerosols in Namibia: a case study analysis from the AEROCLO-sA campaign
Fossil-Dominated SOA Formation in Coastal China: Size-Divergent Pathways of Aqueous Fenton Reactions versus Gas-phase VOC Autoxidation
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
Hydroxymethanesulfonate (HMS) Formation under Urban and Marine Atmosphere: role of aerosol ionic strength
Measurement report: Vertically resolved atmospheric properties observed over the Southern Great Plains with the ArcticShark uncrewed aerial system
Unraveling Arctic submicron organic aerosol sources: a year-long study by H-NMR and AMS in Ny-Ålesund, Svalbard
Non-biogenic sources are an important but overlooked contributor to aerosol isoprene-derived organosulfates during winter in northern China
Unveiling single-particle composition, size, shape, and mixing state of freshly emitted Icelandic dust via electron microscopy analysis
The Critical Role of Volatile Organic Compounds Emission in Nitrate Formation in Lhasa, Tibetan Plateau: Insights from Oxygen Isotope Anomaly Measurements
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
Climatology of aerosol pH and its controlling factors at the Melpitz continental background site in central Europe
Atmospheric chemistry in East Asia determines the iron solubility of aerosol particles supplied to the North Pacific Ocean
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
Yuan Cheng, Ying-jie Zhong, Zhi-qing Zhang, Xu-bing Cao, and Jiu-meng Liu
Atmos. Chem. Phys., 25, 8493–8505, https://doi.org/10.5194/acp-25-8493-2025, https://doi.org/10.5194/acp-25-8493-2025, 2025
Short summary
Short summary
As an emerging hotspot of atmospheric sciences, northeastern 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 in the exploration of PM2.5 sources in northeastern China, which are essential for further improving the regional air quality.
Theresa Mathes, Heather Guy, John Prytherch, Julia Kojoj, Ian Brooks, Sonja Murto, Paul Zieger, Birgit Wehner, Michael Tjernström, and Andreas Held
Atmos. Chem. Phys., 25, 8455–8474, https://doi.org/10.5194/acp-25-8455-2025, https://doi.org/10.5194/acp-25-8455-2025, 2025
Short summary
Short summary
The Arctic is warming faster than the global average and an investigation of aerosol–cloud–sea ice interactions is crucial for studying its climate system. During the ARTofMELT Expedition 2023, particle and sensible heat fluxes were measured over different surfaces. Wide lead surfaces acted as particle sources, with the strongest sensible heat fluxes, while closed ice surfaces acted as particle sinks. In this study, methods to measure these interactions are improved, enhancing our understanding of Arctic climate processes.
Mutian Ma, Laura-Hélèna Rivellini, Yichen Zong, Markus Kraft, Liya E. Yu, and Alex King Yin Lee
Atmos. Chem. Phys., 25, 8185–8211, https://doi.org/10.5194/acp-25-8185-2025, https://doi.org/10.5194/acp-25-8185-2025, 2025
Short summary
Short summary
This work advances our understanding of the 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.
Capucine Camin, François Lacan, Catherine Pradoux, Marie Labatut, Anne Johansen, and James W. Murray
Atmos. Chem. Phys., 25, 8213–8228, https://doi.org/10.5194/acp-25-8213-2025, https://doi.org/10.5194/acp-25-8213-2025, 2025
Short summary
Short summary
This paper presents the chemical and iron isotopic composition of aerosols (> 1 µm) over the equatorial and tropical Pacific Ocean in previously undocumented areas. Analysis of our data suggests that a significant proportion of aerosol iron (∼ 13 %) is not only dissolved but also removed during atmospheric transport. Such removal had not previously been evidenced to our knowledge. This highlights the unique and strong constraints brought by iron isotopes on atmospheric process studies.
Fredrik Mattsson, Almuth Neuberger, Liine Heikkinen, Yvette Gramlich, Marco Paglione, Matteo Rinaldi, Stefano Decesari, Paul Zieger, Ilona Riipinen, and Claudia Mohr
Atmos. Chem. Phys., 25, 7973–7989, https://doi.org/10.5194/acp-25-7973-2025, https://doi.org/10.5194/acp-25-7973-2025, 2025
Short summary
Short summary
This study investigated aerosol–cloud interactions, focusing on organic nitrogen (ON) formation in the aqueous phase. Measurements were conducted in wintertime in the Po Valley, Italy, 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.
Ren-Guo Zhu, Hua-Yun Xiao, Meiju Yin, Hao Xiao, Zhongkui Zhou, Yuanyuan Pan, Guo Wei, and Cheng Liu
Atmos. Chem. Phys., 25, 7699–7718, https://doi.org/10.5194/acp-25-7699-2025, https://doi.org/10.5194/acp-25-7699-2025, 2025
Short summary
Short summary
The concentrations and δ15N isotopic values of CAAs (combined amino acids) in surface soil and plants from the Gobi Desert, as well as in PM2.5 samples from four cities in Northern China, were measured. CAAs transported by Gobi dust were rich in alanine, glycine and glutamic acid. Glycine and leucine in Gobi Desert sources exhibited δ15N depletion by more than 6 ‰ compared to their values in urban PM2.5. Substantial protein-N deposition can be transported by the Gobi Desert to northern China over brief periods.
Yu Huang, Xingru Li, Dan Dan Huang, Ruoyuan Lei, Binhuang Zhou, Yunjiang Zhang, and Xinlei Ge
Atmos. Chem. Phys., 25, 7619–7645, https://doi.org/10.5194/acp-25-7619-2025, https://doi.org/10.5194/acp-25-7619-2025, 2025
Short summary
Short summary
This work comprises a comprehensive investigation into the chemical and optical properties of brown carbon (BrC) in PM2.5 samples collected in Nanjing, China. In particular, we used a machine learning approach to identify a list of key BrC species, which can be a good reference for future studies. Our findings extend understanding of BrC properties and are valuable to the assessment of BrC's impact on air quality and radiative forcing.
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
Atmos. Chem. Phys., 25, 7485–7498, https://doi.org/10.5194/acp-25-7485-2025, https://doi.org/10.5194/acp-25-7485-2025, 2025
Short summary
Short summary
We developed a machine-learning-based method to reconstruct missing elemental carbon (EC) data in four Chinese cities from 2013 to 2023. Using machine learning, we 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.
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
Atmos. Chem. Phys., 25, 7053–7069, https://doi.org/10.5194/acp-25-7053-2025, https://doi.org/10.5194/acp-25-7053-2025, 2025
Short summary
Short summary
Intermediate-volatility/semi-volatile organic compounds in 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 potential tracers for heavy fuel oil exhausts.
Hongyu Zhang, Shenbo Wang, Zhangsen Dong, Xiao Li, and Ruiqin Zhang
Atmos. Chem. Phys., 25, 6943–6955, https://doi.org/10.5194/acp-25-6943-2025, https://doi.org/10.5194/acp-25-6943-2025, 2025
Short summary
Short summary
Analyzing 12-year Zhengzhou data revealed post-2019 crustal material rebound caused by soil dust resuspension, elevating particle pH. Similar coarse particle increases are observed across cities of the North China Plain. Long-term particle acidity evolution in this region requires an integrated assessment of interactions among acidic precursors, ammonia, and crustal components.
Yanqin Ren, Zhenhai Wu, Fang Bi, Hong Li, Haijie Zhang, Junling Li, Rui Gao, Fangyun Long, Zhengyang Liu, Yuanyuan Ji, and Gehui Wang
Atmos. Chem. Phys., 25, 6975–6990, https://doi.org/10.5194/acp-25-6975-2025, https://doi.org/10.5194/acp-25-6975-2025, 2025
Short summary
Short summary
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.
Lise Le Berre, Brice Temime-Roussel, Grazia Maria Lanzafame, Barbara D'Anna, Nicolas Marchand, Stéphane Sauvage, Marvin Dufresne, Liselotte Tinel, Thierry Leonardis, Joel Ferreira de Brito, Alexandre Armengaud, Grégory Gille, Ludovic Lanzi, Romain Bourjot, and Henri Wortham
Atmos. Chem. Phys., 25, 6575–6605, https://doi.org/10.5194/acp-25-6575-2025, https://doi.org/10.5194/acp-25-6575-2025, 2025
Short summary
Short summary
A summer campaign in a Mediterranean port examined pollution caused by ships. Two stations in the port measured pollution levels and captured over 350 ship plumes to study their chemical composition. Results showed that pollution levels, such as ultra-fine particles, were higher in the port than in the city and offer strong support to improve emission inventories. These findings may also serve as reference to assess the benefits of a sulfur Emission Control Area in the Mediterranean in 2025.
Jiayin Li, Tianyu Zhai, Xiaorui Chen, Haichao Wang, Shuyang Xie, Shiyi Chen, Chunmeng Li, Yuanjun Gong, Huabin Dong, and Keding Lu
Atmos. Chem. Phys., 25, 6395–6406, https://doi.org/10.5194/acp-25-6395-2025, https://doi.org/10.5194/acp-25-6395-2025, 2025
Short summary
Short summary
We directly measured the dinitrogen pentoxide (N2O5) uptake coefficient using an aerosol flow tube, which critically impacts the NOx fate and particulate nitrate formation in a typical highland city, Kunming, in China. We found that the performance of current γ (N2O5) parameterizations showed deviations with the varying aerosol liquid water content (ALWC). Such differences would lead to biased estimation of particulate nitrate production potential. We give suggestions for future research directions.
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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.
Yunfeng He, Xiang Ding, Quanfu He, Yuqing Zhang, Duohong Chen, Tao Zhang, Kong Yang, Junqi Wang, Qian Cheng, Hao Jiang, Zirui Wang, Ping Liu, Xinming Wang, and Michael Boy
EGUsphere, https://doi.org/10.5194/egusphere-2025-2204, https://doi.org/10.5194/egusphere-2025-2204, 2025
Short summary
Short summary
The long-term field measurements in the Pearl River Delta revealed a significant decline in PM2.5 main components. As air quality improved, secondary species became more dominant. In addition, the proportion of nitrate had doubled. The changes in chemical composition led to the reductions in aerosol acidity, liquid water content and light extinction coefficient. Our results help to improve understanding of the secondary species formation under decreasing anthropogenic emissions.
Kouji Adachi, Atsushi Yoshida, Tatsuhiro Mori, Nobuhiro Moteki, Sho Ohata, Kazuyuki Kita, Yoshimi Kawai, and Makoto Koike
EGUsphere, https://doi.org/10.5194/egusphere-2025-2230, https://doi.org/10.5194/egusphere-2025-2230, 2025
Short summary
Short summary
This study measured the compositions and mixing states of individual aerosol particles collected at different altitudes over the western North Pacific by simultaneous sampling from an aircraft and a research vessel. The results showed that they were strongly influenced by Siberian Forest biomass burning and mixed with sea spray, and identified various aerosol compositions at different altitudes, sizes, and aerosol sources, highlighting a wide range of individual particle compositions.
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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.
Tao Qiu, Yanting Qiu, Yongyi Yuan, Rui Su, Xiangxinyue Meng, Jialiang Ma, Xiaofan Wang, Yu Gu, Zhijun Wu, Yang Ning, Xiuyi Hua, Dapeng Liang, and Deming Dong
EGUsphere, https://doi.org/10.5194/egusphere-2025-1808, https://doi.org/10.5194/egusphere-2025-1808, 2025
Short summary
Short summary
Our research reveals that some species from biomass burning and coal combustion dominate the light absorption of organic aerosols during winter. Cold weather helps these species accumulate in aerosols by slowing their degradation and altering atmospheric chemical processes. This means colder regions might experience stronger and more persistent climate impacts. Our findings highlight the importance of local temperatures and pollution sources when tackling climate challenges.
Can Wu, Yubao Chen, Yuwei Sun, Huijun Zhang, Si Zhang, Cong Cao, Jianjun Li, and Gehui Wang
EGUsphere, https://doi.org/10.5194/egusphere-2025-1668, https://doi.org/10.5194/egusphere-2025-1668, 2025
Short summary
Short summary
Biogenic secondary organic aerosol (BSOA), as an important atmospheric component, is prevalent within the boundary layer and can influence air quality and human health. Our observations demonstrate that anthropogenic NOx and the enhanced aerosol water driven by sulfate inhibit BSOA formation in lifting air masses, leading to a moderate reduction in the SOA burden in the upper boundary layer.
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
Short summary
Short summary
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.
Paola Formenti, Chiara Giorio, Karine Desboeufs, Alexander Zherebker, Marco Gaetani, Clarissa Baldo, Gautier Landrot, Simona Montebello, Servanne Chevaillier, Sylvain Triquet, Guillaume Siour, Claudia Di Biagio, Francesco Battaglia, Jean-François Doussin, Anais Feron, Andreas Namwoonde, and Stuart John Piketh
EGUsphere, https://doi.org/10.5194/egusphere-2025-446, https://doi.org/10.5194/egusphere-2025-446, 2025
Short summary
Short summary
The elemental composition and solubility of several metals, including iron, at a coastal site in Namibia in August–September 2017, indicate that natural and anthropogenic dust had different solubility depending on mineralogy but mostly to the processing by fluoride ions from marine emissions, pointing out to the complexity of atmospheric/oceanic interactions in this region of the world influenced by the Benguela current and significant aerosol load.
Jia-Yuan Wang, Meng-Xue Tang, Shan Lu, Ke-Jin Tang, Xing Peng, Ling-Yan He, and Xiao-Feng Huang
EGUsphere, https://doi.org/10.5194/egusphere-2025-1034, https://doi.org/10.5194/egusphere-2025-1034, 2025
Short summary
Short summary
Our study explores how secondary organic aerosols (SOA), a major component of air pollution, form in different particle sizes in a coastal city in China. We found that SOA in fine particles is mainly produced through aqueous chemical reactions, especially those involving iron. In contrast, coarse particles form SOA through reactions with ozone and gases from both fossil fuels and natural sources. These findings highlight the need for size-specific air pollution models.
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
Short summary
Short summary
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
Short summary
Short summary
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.
Rongshuang Xu, Yu-Chi Lin, Siyu Bian, Feng Xie, and Yan-Lin Zhang
EGUsphere, https://doi.org/10.5194/egusphere-2025-683, https://doi.org/10.5194/egusphere-2025-683, 2025
Short summary
Short summary
This work reported the hydroxymethanesulfonate (HMS) level in a continental city and, for the first time, in marine atmosphere. The enhancement by aerosol ionic strength (IS) on HMS formation was quantified which first rise with increasing IS, peaking at 4 mol kg–1 before declining. Given the IS range of marine (2–6) and urban aerosol (6–20 mol kg–1) and the clearly negative correlation between humidity and IS, the moderate IS level under humid condition may notably boost ambient HMS formation.
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
Short summary
Short summary
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.
Marco Paglione, Yufang Hao, Stefano Decesari, Mara Russo, Karam Mansour, Mauro Mazzola, Diego Fellin, Andrea Mazzanti, Emilio Tagliavini, Manousos Ioannis Manousakas, Evangelia Diapouli, Elena Barbaro, Matteo Feltracco, Kaspar Rudolf Daellenbach, and Matteo Rinaldi
EGUsphere, https://doi.org/10.5194/egusphere-2025-760, https://doi.org/10.5194/egusphere-2025-760, 2025
Short summary
Short summary
A year-long set of PM1 samples from Ny-Ålesund, Svalbard, was analyzed by H-NMR and HR-TOF-AMS for the chemical characterization of the organic fraction. Positive Matrix Factorization allowed to identify five organic aerosol sources with specific seasonality. Winter-spring aerosol is dominated by Eurasian pollution, while summer is characterized by biogenic aerosols from marine sources; occasional summertime high OA loadings are associated with wildfire aerosols.
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
Short summary
Short summary
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.
Agnesh Panta, Konrad Kandler, Kerstin Schepanski, Andres Alastuey, Pavla Dagsson Waldhauserova, Sylvain Dupont, Melanie Eknayan, Cristina González-Flórez, Adolfo González-Romero, Martina Klose, Mara Montag, Xavier Querol, Jesús Yus-Díez, and Carlos Pérez García-Pando
EGUsphere, https://doi.org/10.5194/egusphere-2025-494, https://doi.org/10.5194/egusphere-2025-494, 2025
Short summary
Short summary
Iceland is among the most active dust source areas in the world. Dust properties are influenced by particle size, mineralogy, shape, and mixing state. This work characterizes freshly emitted individual aerosol particles of Icelandic dust using electron microscopy. Our study provides insights into critical particle-specific information will contribute to better constraining climate models that consider mineralogical variations in their representation of the dust cycle.
Xueqin Zheng, Junwen Liu, Nima Chuduo, Bian Ba, Pengfei Yu, Phu Drolgar, Fang Cao, and Yanlin Zhang
EGUsphere, https://doi.org/10.5194/egusphere-2025-164, https://doi.org/10.5194/egusphere-2025-164, 2025
Short summary
Short summary
In this study, we present the first report on the annual variation of stable oxygen isotope anomalies (∆17O = δ17O - 0.52 × δ18O) in NO3- collected from the urban area of Lhasa , on the Tibetan Plateau, China. Using a Bayesian isotope mixture model, we found that the relative contribution of the NO3+VOC pathway to NO3- formation in spring in Lhasa was several times higher than in urban cities, highlighting the significant influence of VOC transported from outside the Tibetan Plateau.
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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.
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
Short summary
Short summary
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.
Kohei Sakata, Shotaro Takano, Atsushi Matsuki, Yasuo Takeichi, Hiroshi Tanimoto, Aya Sakaguchi, Minako Kurisu, and Yoshio Takahashi
EGUsphere, https://doi.org/10.5194/egusphere-2025-161, https://doi.org/10.5194/egusphere-2025-161, 2025
Short summary
Short summary
Deposition of aerosol iron (Fe) into the ocean stimulates primary production and influences the global carbon cycle, although the factors governing the aerosol Fe solubility remain uncertain. Our observations in Japan revealed that both mineral dust and anthropogenic aerosols are significant sources of dissolved Fe, and that atmospheric chemical weathering enhances their solubility. This finding is expected to play a crucial role in estimating the supply of dissolved iron to the ocean.
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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.
Cited articles
Albrecht, B.: Aerosols, cloud microphysics and fractional cloudiness, Science, 245, 1227–1230, 1989.
Allen, T.: Particle Size Measurement: Volume 1, Chapman & Hall, London, 1997.
Ayers, G. P.: Quantitative determination of sulfate in individual aerosol particles, Atmos. Environ. 12, 1613–1621, 1978.
Barnard, W. R., Andreae, M. O., and Iverson, R. L.: Dimethylsulfide and Phaeocystis pouchetii in the southeastern Bering Sea, Cont. Shelf Res., 3, 103–113, 1984.
Bates, T. S., Cline, J. D., Gammon, R. H., and Kelly-Hansen, S. R.: Regional and seasonal variations in the flux of oceanic dimethylsulfide to the atmosphere, J. Geophys. Res., 92, 2930–2938, https://doi.org/10.1029/JC092iC03p02930, 1987.
Bigg, E. K.: Comparison of Aerosol at Four Baseline Atmospheric Monitoring Stations, J. Appl. Meteorol., 19, 521–533, 1980.
Bigg, E. K.: Ammonium compounds in stratospheric aerosols, Tellus B, 38, 62–66, 1986.
Bigg, E. K. and Leck, C.: Cloud-active particles over the central Arctic Ocean, J. Geophys. Res., 106, 32155–32166, https://doi.org/10.1029/1999JD901152, 2001a.
Bigg, E. K. and Leck, C.: Properties of the aerosol over the central Arctic Ocean, J. Geophys. Res., 106, 32101–32109, https://doi.org/10.1029/1999JD901136, 2001b.
Bigg, E. K. and Leck, C.: The composition of fragments of bubbles bursting at the ocean surface, J. Geophys. Res. 113, D11209, https://doi.org/10.1029/2007JD009078, 2008.
Bigg, E. K., Ono, A., and Williams, J. A.: Chemical tests for individual submicron aerosol particles, Atmos. Environ., 8, 1–13, 1974.
Bigg, E. K., Leck, C., and Nilsson, E. D.: Sudden changes in arctic atmospheric aerosol concentrations during summer and autumn, Tellus B, 48, 254–271, https://doi.org/10.1034/j.1600-0889.1996.t01-1-00009.x, 1996.
Bigg, E. K., Leck, C., and Tranvik, L.: Particulates of the surface microlayer of open water in the central Arctic Ocean in summer, Mar. Chem., 91, 131–141, 2004.
Blanchard, D. C.: The oceanic production of volatile cloud nuclei, J. Atmos. Sci., 28, 811–812, https://doi.org/10.1175/1520-0469(1971)028<0811:TOPOVC>2.0.CO;2, 1971.
Blanchard, D. C. and Syzdeck, L. D.: Filmdrop production as a function of bubble size, J. Geophys. Res., 93, 3649–3654, https://doi.org/10.1029/JC093iC04p03649, 1988.
Blanchard, D. C. and Woodcock, A. H.: Bubble formation and modification in the sea and its meteorological significance, Tellus, 9, 145–158, https://doi.org/10.1111/j.2153-3490.1957.tb01867.x, 1957.
Busek, P. R. and Pósfai, M.: Airborne minerals and related aerosol particles: effects on climate and the environment, P. Natl. Acad. Sci. USA, 96, 3372–3379, 1999.
Capaldo, K. P. and Pandis, S. N.: Dimethylsulfide chemistry in the remote marine atmosphere: Evaluation and sensitivity analysis of available mechanisms, J. Geophys. Res., 102, 23251–23267, 1997.
Carslaw, K. S., Lee, A., Reddington, C. L., Pringle, K. J., Rap, A., Forster, P. M., Mann, G. W., Spracklen, D. V., Woodhouse, M. T., Regayre, L. A., and Pierce, J. R.: Large contribution of natural aerosols to uncertainty in indirect forcing, Nature, 503, 67–71, https://doi.org/10.1038/nature12674, 2013.
Chi, J. W., Li, W. J., Zhang, D. Z., Zhang, J. C., Lin, Y. T., Shen, X. J., Sun, J. Y., Chen, J. M., Zhang, X. Y., Zhang, Y. M., and Wang, W. X.: Sea salt aerosols as a reactive surface for inorganic and organic acidic gases in the Arctic troposphere, Atmos. Chem. Phys., 15, 11341–11353, https://doi.org/10.5194/acp-15-11341-2015, 2015.
Chin, W.-C., Orellana, M. V., and Verdugo, P.: Spontaneous assembly of marine dissolved organic matter into polymer gels, Nature, 391, 568–572, 1998.
Covert, D. S., Wiedensohler, A., Aalto, P., Heintzenberg, J., McMurry, P. H., and Leck, C.: Aerosol number size distributions from 3 to 500 nm diameter in the arctic marine boundary layer during summer and autumn, Tellus B, 48, 197–212, 1996.
Ding, Y.-X., Chin, W.-C., Rodriguez, A., Hung, C.-C., Santschi, P. H., and Verdugo, P.: Amphiphilic exopolymers from Sagittula stellata induce DOM self-assembly and formation of marine microgels, Mar. Chem., 112, 11–19, 2008.
Dixkens, J. and Fissan, H.: Development of an Electrostatic Precipitator for Off-Line Particle Analysis, Aerosol. Sci. Tech., 30, 438–453, 1999.
Douglas, T. and Sturm, M.: Arctic haze, mercury and the chemical composition of snow across northwestern Alaska, Atmos. Environ., 38, 805–820, 2004.
Egerton, R. F.: Physical Principles of Electron Microscopy, Springer, New York, USA, 2008.
Engvall, A.-C., Krejci, R., Ström, J., Treffeisen, R., Scheele, R., Hermansen, O., and Paatero, J.: Changes in aerosol properties during spring-summer period in the Arctic troposphere, Atmos. Chem. Phys., 8, 445–462, https://doi.org/10.5194/acp-8-445-2008, 2008.
Farlow, N. H., Hayes, D. M., and Lem, H. Y.: Stratospheric aerosols: undissolved granules and physical state, J. Geophys. Res., 82, 4921–4929, 1977.
Ferek, R. J., Lazrus, A. L., and Winchester, W.: Electron microscopy of acidic aerosols collected over the northeastern United States, Atmos. Environ., 17, 1545–1561, 1983.
Forster, P., Ramaswamy, V., Artaxo, P., Berntsen, T., Betts, R., Fa- hey, D. W., Haywood, J., Lean, J., Lowe, D. C., Myhre, G., Nganga, J., Prinn, R., Raga, G., Schulz, M., and Van Dorland, R.: Changes in atmospheric constituents and in radiative forcing, in: Climate Change 2007: The Physical Science Basis. Contribution of Working Group I to the Fourth Assessment Report of the Intergovernmental Panel on Climate Change, edited by: Solomon, S., Qin, D., Manning, M., Chen, Z., Marquis, M., Averyt, K. B., Tignor, M., and Miller, H. L., Cambridge University Press, Cambridge, United Kingdom and New York, NY, USA, 2007.
Geng, H., Ryu, J., Jung, H.-J., Chung, H., Ahn, K.-H., and Ro, C.-U.: Single-Particle Characterization of Summertime Arctic Aerosols Collected at Ny-Alesund, Svalbard, Environ. Sci. Technol., 44, 2348–2353, 2010.
Gershey, R. M.: Characterization of seawater organic matter carried by bubble generated aerosols, Limnol. Oceanogr., 28, 309–319, https://doi.org/10.4319/lo.1983.28.2.0309, 1983.
Hamacher-Barth, E., Jansson, K., and Leck, C.: A method for sizing submicrometer particles in air collected on Formvar films and imaged by scanning electron microscope, Atmos. Meas. Tech., 6, 3459–3475, https://doi.org/10.5194/amt-6-3459-2013, 2013.
Hara, K., Yamagata, S., Yamanouchi, T., K. Sato, K., Herber, A., Iwasaka, Y., Nagatani, M., and Nakata, H.: Mixing states of individual aerosol particles in spring Arctic troposphere during ASTAR 2000 campaign, J. Geophys. Res.-Atmos., 108, 4209, https://doi.org/10.1029/2002JD002513, 2003.
Heard, M. J. and Wiffen, R. D.: Electron microscopy of natural aerosols and the identification of particulate ammonium sulfate, Atmos. Environ., 3, 337–340, 1969.
Heintzenberg, J. and Leck, C.: Seasonal variations of the atmospheric aerosol near the top of the marine boundary layer over Spitsbergen related to the Arctic sulfur cycle, Tellus B, 46, 52–67, 1994.
Heintzenberg, J. and Leck, C.: The summer aerosol in the central Arctic 1991–2008: did it change or not?, Atmos. Chem. Phys., 12, 3969–3983, https://doi.org/10.5194/acp-12-3969-2012, 2012.
Heintzenberg, J., Leck, C., Birmili, W., Wehner, B., Tjernström, M., and Wiedensohler, A.: Aerosol number-size distributions during clear and fog periods in the summer high Arctic: 1991, 1996 and 2001, Tellus B, 58, 41–50, https://doi.org/10.1111/j.1600-0889.2005.00171.x, 2006.
Heintzenberg, J., Leck, C., and Tunved, P.: Potential source regions and processes of aerosol in the summer Arctic, Atmos. Chem. Phys., 15, 6487–6502, https://doi.org/10.5194/acp-15-6487-2015, 2015.
Held, A., Brooks, I. M., Leck, C., and Tjernström, M.: On the potential contribution of open lead particle emissions to the central Arctic aerosol concentration, Atmos. Chem. Phys., 11, 3093–3105, https://doi.org/10.5194/acp-11-3093-2011, 2011a.
Held, A., Orsini, D. A., Vaattovaara, P., Tjernström, M., and Leck, C.: Near-surface profiles of aerosol number concentration and temperature over the Arctic Ocean, Atmos. Meas. Tech., 4, 1603–1616, https://doi.org/10.5194/amt-4-1603-2011, 2011b.
Hillamo, R., Kerminen, V.-M., Aurela, M., Mäkelä, T., Maenhaut, W., and Leck, C.: Modal structure of chemical mass size distribution in the high Arctic aerosol, J. Geophys. Res., 106, 27555–27571, https://doi.org/10.1029/2001JD001119, 2001.
Hinds, W.: Aerosol Technology, 2nd Edn., John Wiley & Sons, New York, 1999.
Hoppel, W. A., Frick, G. M., and Larson, R. E.: Effect of nonprecipitating clouds on the aerosol size distribution in the marine boundary layer, Geophys. Res. Lett., 13, 125–128, 1986.
Johnson, B. D. and Wangersky, P. J.: Microbubbles – stabilization by monolayers of adsorbed particles, J. Geophys. Res.-Oceans, 92, 14641–14647, https://doi.org/10.1029/JC092iC13p14641, 1987.
Karl, M., Leck, C., Coz, E., and Heintzenberg, J.: Marine nanogels as a source of atmospheric nanoparticles in the high Arctic, Geophys. Res. Lett., 40, 3738–3743, 2013.
Kettle, A. J., Andreae, M. O., Amouroux, D., Andreae, T. W., Bates, T. S., Berresheim, H., Bingemer, H., Boniforti, R., Curran, M. A. J., DiTullio, G. R., Helas, G., Jones, G. B., Keller, M. D., Kiene, R. P., Leck, C., Levasseur, M., Maspero, M., Matrai, P., McTaggat, A. R., Mihalopoulos, N., Nguyen, B. C., Novo, A., Putaud, J. P., Rapsomanikis, S., Roberts, G., Schebeske, G., Sharma, S., Simo, R., Staubes, R., Turner, S., and Uher, G.: A global database of sea surface dimethylsulphide (DMS) measurements and a simple model to predict sea surface DMS as a function of latitude, longitude and month, Global Biogeochem. Cy., 13, 399–444, 1999.
Korhonen, H., Carslaw, K. S., Spracklen, D. V., Ridley, D. A., and Ström, J.: A global model study of processes controlling aerosol size distributions in the Arctic spring and summer, J. Geophys. Res., 113, D08211, https://doi.org/10.1029/2007JD009114, 2008.
Kuhn, T., Damoah, R., Bacak, A., and Sloan, J. J.: Characterising aerosol transport into the Canadian High Arctic using aerosol mass spectrometry and Lagrangian modelling, Atmos. Chem. Phys., 10, 10489–10502, https://doi.org/10.5194/acp-10-10489-2010, 2010.
Lannefors, H., Heintzenberg, J., and Hansson, H.-C.: A comprehensive study of physical and chemical parameters of the Arctic summer aerosol; results from the Swedish expedition Ymer-80, Tellus B, 35, 40–54, 1983.
Leck, C. an Bigg, E. K.: Aerosol production over remote marine areas – a new route, Geophys. Res. Lett., 26, 3577–3580, 1999.
Leck, C. and Bigg, E. K.: Evolution of marine aerosol – a new perspective, Geophys. Res. Lett., 32, L19803, https://doi.org/10.1029/2005GL023651, 2005a.
Leck, C. and Bigg, E. K.: Biogenic particles in the surface microlayer and overlaying atmosphere in the central Arctic Ocean during summer, Tellus B, 57, 305–316, https://doi.org/10.1111/j.1600-0889.2005.00148.x, 2005b.
Leck, C. and Bigg, E. K.: Comparison of sources and nature of the tropical aerosol with the summer high Arctic aerosol, Tellus B, 60, 118–126, 2008.
Leck, C. and Bigg, E. K.: New particle formation of marine biological origin, Aerosol Sci. Tech., 44, 570–577, 2010.
Leck, C. and Nilsson, D. E.: A pseudo-Lagrangian study of the sulfur budget in the remote Arctic marine boundary layer, Tellus B, 54, 213–230, 2002.
Leck, C. and Svensson, E.: Importance of aerosol composition and mixing state for cloud droplet activation over the Arctic pack ice in summer, Atmos. Chem. Phys., 15, 2545–2568, https://doi.org/10.5194/acp-15-2545-2015, 2015.
Leck, C., Bigg, E. K., Covert, D. S., Heintzenberg, J., Maenhaut, W., Nilsson, E. D., and Wiedensohler, A.: Overview of the atmospheric research program during the International Arctic Ocean Expedition 1991 (IAOE-91) and its scientific results, Tellus B, 48, 136–155, 1996.
Leck, C., Nilsson, E. D., Bigg, E. K., and Bäcklin, L.: The atmospheric program of the Arctic Ocean Expedition 1996 (AOE-96): An overview of scientific goals, experimental approach, and instruments, J. Geophys. Res., 106, 32051–32067, 2001.
Leck, C., Norman, M., Bigg, E. K., and Hillamo, R.: Chemical composition and sources of the high Arctic aerosol relevant for cloud formation, J. Geophys. Res., 107, 4135–4153, https://doi.org/10.1029/2001JD001463, 2002.
Leck, C., Tjernström, M., Matrai, P., Swietlicki, E., and Bigg, E. K.: Can marine micro-organisms influence melting of the Arctic pack ice?, EOS, 85, 25–36, 2004.
Leck, C., Gao, Q., Mashayekhy Rad, F., and Nilsson, U.: Size-resolved atmospheric particulate polysaccharides in the high summer Arctic, Atmos. Chem. Phys., 13, 12573–12588, https://doi.org/10.5194/acp-13-12573-2013, 2013.
Lee, L. A., Pringle, K. J., Reddington, C. L., Mann, G. W., Stier, P., Spracklen, D. V., Pierce, J. R., and Carslaw, K. S.: The magnitude and causes of uncertainty in global model simulations of cloud condensation nuclei, Atmos. Chem. Phys., 13, 8879–8914, https://doi.org/10.5194/acp-13-8879-2013, 2013.
Li, X., Leck, C., Sun, L., Hede, T., Tu, Y., and Ågren, H.: Cross-linked polysaccharide assemblies in marine gels: an atomistic simulation, J. Phys. Chem. Lett., 4, 2637–2642, https://doi.org/10.1021/jz401276r, 2013.
Lohmann, U. and Leck, C.: Importance of submicron surface-active organic aerosols for pristine Arctic clouds, Tellus B, 57, 261–268, 2005.
Maitra, U., Mukhpadhyay, S., Sarkar, A., Rao, P., and Indi, S. S.: Hydrophobic pockets in a nonpolymeric aqueous gel: observation of such a gelation process by color change, Angew. Chem. Int., 40, 2281–2283, 2001.
Mancuso-Nichols, C. A., Guezennec, J., and Bowman, J. P.: Bacterial exopolysaccharides from extreme marine environments, with special consideration of the Southern Ocean, sea ice and hydrothermal vents: a review, J. Appl. Microbiol., 96, 1057–1066, 2005.
Mann, G. W., Carslaw, K. S., Reddington, C. L., Pringle, K. J., Schulz, M., Asmi, A., Spracklen, D. V., Ridley, D. A., Woodhouse, M. T., Lee, L. A., Zhang, K., Ghan, S. J., Easter, R. C., Liu, X., Stier, P., Lee, Y. H., Adams, P. J., Tost, H., Lelieveld, J., Bauer, S. E., Tsigaridis, K., van Noije, T. P. C., Strunk, A., Vignati, E., Bellouin, N., Dalvi, M., Johnson, C. E., Bergman, T., Kokkola, H., von Salzen, K., Yu, F., Luo, G., Petzold, A., Heintzenberg, J., Clarke, A., Ogren, J. A., Gras, J., Baltensperger, U., Kaminski, U., Jennings, S. G., O'Dowd, C. D., Harrison, R. M., Beddows, D. C. S., Kulmala, M., Viisanen, Y., Ulevicius, V., Mihalopoulos, N., Zdimal, V., Fiebig, M., Hansson, H.-C., Swietlicki, E., and Henzing, J. S.: Intercomparison and evaluation of global aerosol microphysical properties among AeroCom models of a range of complexity, Atmos. Chem. Phys., 14, 4679–4713, https://doi.org/10.5194/acp-14-4679-2014, 2014.
Martin, M., Chang, R. Y.-W., Sierau, B., Sjogren, S., Swietlicki, E., Abbatt, J. P. D., Leck, C., and Lohmann, U.: Cloud condensation nuclei closure study on summer arctic aerosol, Atmos. Chem. Phys., 11, 11335–11350, https://doi.org/10.5194/acp-11-11335-2011, 2011.
Mauritsen, T., Sedlar, J., Tjernström, M., Leck, C., Martin, M., Shupe, M., Sjogren, S., Sierau, B., Persson, P. O. G., Brooks, I. M., and Swietlicki, E.: An Arctic CCN-limited cloud-aerosol regime, Atmos. Chem. Phys., 11, 165–173, https://doi.org/10.5194/acp-11-165-2011, 2011.
Medwin, H.: In-situ acoustic measurements of bubble populations in coastal ocean waters, J. Geophys. Res., 75, 599–611, https://doi.org/10.1029/JC075i003p00599, 1970.
Mészáros, A. and Vissy, K.: Concentration, size distribution and chemical nature of atmospheric aerosol particles in remote oceanic areas, J. Aerosol Sci., 5, 101–110, 1974.
Michael, J. R., Joy, D. C., and Griffin, B. J.: Use of sample bias voltage for low-energy high-resolution imaging in the SEM, Microsc. Microanal., 16, 614–615, https://doi.org/10.1017/S1431927610055315, 2010.
Nilsson, D. E. and Leck, C.: A pseudo-Lagrangian study of the sulfur budget in the remote Arctic marine boundary layer, Tellus B, 54, 213–230, 2002.
Norris, S. J., Brooks, I. M., de Leeuw, G., Sirevaag, A., Leck, C., Brooks, B. J., Birch, C. E., and Tjernström, M.: Measurements of bubble size spectra within leads in the Arctic summer pack ice, Ocean Sci., 7, 129–139, https://doi.org/10.5194/os-7-129-2011, 2011.
O'Dowd, C. D., Lowe, J. A., Smith, M. H., and Kaye, M. H.: The relative importance of non-sea-salt sulphate and sea-salt aerosol to the marine cloud condensation nuclei population: An improved multi-component aerosol-cloud droplet parametrization, Q. J. Roy. Meteor. Soc., 125, 1295–1313, 1999.
Okada, K.: Nature of individual hygroscopic particles in the urban atmosphere, J. Meteorol. Soc. Jpn., 61, 727–735, 1983.
Orellana, M. V. and Leck, C.: Marine microgels in: Biogeochemistry of Marine Dissolved Organic Matter, 2nd Edn., 451–480, https://doi.org/10.1016/B978-0-12-405940-5.00009-1, 2015.
Orellana, M. V. and Verdugo, P.: Ultraviolet radiation blocks the organic carbon exchange between the dissolved phase and the gel phase in the ocean, Limnol. Oceanogr., 48, 1618–1623, 2003.
Orellana, M. V., Matrai, P. A., Leck, C., Rauschenberg, C. D., Lee, A. M., and Coz, E.: Marine microgels as a source of cloud condensation nuclei in the high Arctic, P. Natl. Acad. Sci., 108, 13612–13617, https://doi.org/10.1073/pnas.1102457108, 2011.
Ovadnevaite, J., Ceburnis, D., Martucci, G., Bialek, J., Monahan, C., Rinaldi, M., Facchini, M. C., Berresheim, H., Worsnop, D. R., and O'Dowd, C.: Primary marine organic aerosol: A dichotomy of low hygroscopicity and high CCN activity, Geophys. Res. Lett., 38, L21806, https://doi.org/10.1029/2011GL048869, 2011.
Penner, J. E., Andreae, M., Annegarn, H., Barrie, L., Feichter, J., Hegg, D., Jayaraman, A., Leaitch, R., Murphy, D., Nganga, J., and Pitar, G.: Aerosols, their Direct and Indirect Effects, in: Climate Change 2001: The Scientific Basis, Contribution of Working Group I to the Third Assessment Report of the Intergovern- mental Panel on Climate Change, edited by: Houghton, J. T., Ding, Y., Griggs, D. J., Noguer, M., van der Linden, P. J., Dai, X., Maskell, K., and Johnson, C. A., Cambridge University Press, Cambridge, United Kingdom and New York, NY, USA, 2001.
Quinn, P. K., Charlson, R. J., and Zoller, W. H.: Ammonia, the dominant base in the remote marine troposphere: a review, Tellus B, 39, 413–425, 1987.
Rao, K. V. R., Hariharan, P. L., Jagannathan, K., and Yoganarasimhan, S. R.: Scanning electron microscopy of ammonium nitrate prills in relation to their application in ammonium nitrate-fuel oil systems, Fuel, 68, 1118–1122, https://doi.org/10.1016/0016-2361(89)90181-6, 1989.
Rocha, S., Krastev, R., Thünemann, A. F., Pereira, M. C., Möhwald, H., and Bezesinski, G.: Adsorption of amyloid ß-peptide at polymer surfaces: a neutron reflectivity study, Chem. Phys. Chem., 6, 2527–2534, https://doi.org/10.1002/cphc.200500158, 2005.
Schimel, D., Alves, D., Enting, I., Heimann, M., Joos, F., Raynaud, D., Wigley, T., Prather, M., Derwent, R., Ehhalt, D., Fraser, P., Sanhueza, E., Zhou, X., Jonas, P., Charlson, R., Rodhe, H., Sadasivan, S., Shine, K. P., Fouquart, Y., Ramaswamy, V., Solomon, S., Srinivasan, J., Albritton, D., Isaksen, I., Lal, M., and Wuebbles, D.: Radiative forcing of climate change, in: Climate Change 1996, Contribution of Working Group I to the 2nd Assessment Report of the Intergovernmental Panel on Climate Change, edited by: Houghton, J. T., Meira Filho, L. G., Callander, B. A., Harris, N., Kattenberg, A., and Maskell, K., Cambridge University Press, Cambridge, United Kingdom and New York, NY, USA, 1996.
Shaw, G. E.: Microparticle size spectrum of Arctic haze, Geophys. Res. Lett., 11, 409–412, 1984.
Shaw, G. E.: The arctic haze phenomenon, B. Am. Meteorol. Soc., 76, 2403–2413, 1995.
Solomon, S., Quin, D., Manning, M., Chen, Z., Marquis, M., Averyt, K. B., Tignor, M., and Miller, H. L.: Climate change 2007: The physical science basis, Cambridge University Press, 996 pp., 2007.
Söderlund, R.: Ammonia in the atmosphere, PhD dissertation, University of Stockholm, Stockholm, Sweden, 1982.
Stevens, S. M., Jansson, K., Xiao, C., Asahina, S., Klingstedt, M., Grüner, D., Sakamoto, Y., Keiichi, M., Cubillas, P., Brent, R., Han, L., Che, S., Ryoo, R., Zhao, D., Anderson, M., Schüth, F., and Terasaki, O.: An Appraisal of High Resolution Scanning Electron Microscopy to Porous Material, JEOL news, 44, 17-22, 2009.
Stohl, A.: Characteristics of atmospheric transport into the Arctic troposphere, J. Geophys. Res., 111, D11306, https://doi.org/10.1029/2005JD006888, 2006.
Stolzenburg, M. R.: An ultrafine aerosol size distribution measuring system, PhD Thesis, University of Minnesota, Minneapolis, USA, 1988.
Ström, J., Umegård, K., Tørseth, K., Tunved, P., Hansson, H.-C., Holmén, K., Wismann, V., Herver, A., and König-Langlo, G.: One year of particle size distribution and aerosol chemical composition measurements at the Zeppelin station, Svalbard, March 2000–2001, Phys. Chem. Earth, 28, 1181–1190, 2003.
Sun, L., Li, X., Hede, T., Tu, Y., Leck, C., and Ågren, H.: Molecular dynamics simulations reveal the assembly mechanisms of polysaccharides in marine aerosols, Phys. Chem. Chem. Phys., 16, 25935–25941, 2014.
Tanaka, T., Fillmore, D., Sun, S., Nishio, I., Wislow, G. S., and Shah, A.: Phase transitions in ionic gels, Phys. Rev. Lett., 45, 1636–1642, 1980.
Tjernström, M., Birch, C. E., Brooks, I. M., Shupe, M. D., Persson, P. O. G., Sedlar, J., Mauritsen, T., Leck, C., Paatero, J., Szczodrak, M., and Wheeler, C. R.: Meteorological conditions in the central Arctic summer during the Arctic Summer Cloud Ocean Study (ASCOS), Atmos. Chem. Phys., 12, 6863–6889, https://doi.org/10.5194/acp-12-6863-2012, 2012.
Tjernström, M., Leck, C., Birch, C. E., Bottenheim, J. W., Brooks, B. J., Brooks, I. M., Bäcklin, L., Chang, R. Y.-W., de Leeuw, G., Di Liberto, L., de la Rosa, S., Granath, E., Graus, M., Hansel, A., Heintzenberg, J., Held, A., Hind, A., Johnston, P., Knulst, J., Martin, M., Matrai, P. A., Mauritsen, T., Müller, M., Norris, S. J., Orellana, M. V., Orsini, D. A., Paatero, J., Persson, P. O. G., Gao, Q., Rauschenberg, C., Ristovski, Z., Sedlar, J., Shupe, M. D., Sierau, B., Sirevaag, A., Sjogren, S., Stetzer, O., Swietlicki, E., Szczodrak, M., Vaattovaara, P., Wahlberg, N., Westberg, M., and Wheeler, C. R.: The Arctic Summer Cloud Ocean Study (ASCOS): overview and experimental design, Atmos. Chem. Phys., 14, 282—2869, https://doi.org/10.5194/acp-14-2823-2014, 2014.
Twomey, S. A.: The influence of pollution on the shortwave albedo of clouds, J. Atmos. Sci., 34, 1149–1152, 1977.
Verdugo, P.: Marine microgels, Annu. Rev. Mar. Sci., 4, 375–400, 2012.
Verdugo, P., Alldredge, A. L., Azam, F., Kirchman, D. L., Passow, U., and Santschi, P. H.: The oceanic gel phase: a bridge in the DOM-POM continuum, Mar. Chem., 92, 67–85, 2004.
Wettlaufer, J. S.: Introduction to Crystallization Phenomena in Natural and Artificial Sea Ice, in: Physics of Ice-Covered Seas, edited by: Lepparanta, M., University of Helsinki Press, Helsinki, 105–194, 1998.
Wiedensohler, A., Birmili, W., Nowak, A., Sonntag, A., Weinhold, K., Merkel, M., Wehner, B., Tuch, T., Pfeifer, S., Fiebig, M., Fjäraa, A. M., Asmi, E., Sellegri, K., Depuy, R., Venzac, H., Villani, P., Laj, P., Aalto, P., Ogren, J. A., Swietlicki, E., Williams, P., Roldin, P., Quincey, P., Hüglin, C., Fierz-Schmidhauser, R., Gysel, M., Weingartner, E., Riccobono, F., Santos, S., Grüning, C., Faloon, K., Beddows, D., Harrison, R., Monahan, C., Jennings, S. G., O'Dowd, C. D., Marinoni, A., Horn, H.-G., Keck, L., Jiang, J., Scheckman, J., McMurry, P. H., Deng, Z., Zhao, C. S., Moerman, M., Henzing, B., de Leeuw, G., Löschau, G., and Bastian, S.: Mobility particle size spectrometers: harmonization of technical standards and data structure to facilitate high quality long-term observations of atmospheric particle number size distributions, Atmos. Meas. Tech., 5, 657–685, https://doi.org/10.5194/amt-5-657-2012, 2012.
Williams, D. B. and Carter, C. B.: Transmission Electron Microscopy, A textbook for materials science, Part I: Transmission electron microscopy, Springer Science + Buisiness Media, New York, USA, 354 pp., 1996.
Winiger, P., Andersson, A., Yttri, K. E., Tunved, P., and Gustafsson, Ö.: Isotope-based source appointment of EC aerosol particles during winter high-pollution events at the Zeppelin Observatory, Svalbard, Environ. Sci. Techol., 49, 11959–11966, https://doi.org/10.1021/acs.est.5b02644, 2015.
Wotton, R. S. and Preston, T. M.: Surface films – areas of water bodies that are often overlooked, BioScience, 55, 137–145, 2005.
Xie, Z., Blum, J. D., Utsunomiya, S., Ewing, R. C., Wang, X., and Sun, L.: Summertime carbonaceous aerosols collected in the marine boundary layer of the Arctic Ocean, J. Geophys. Res., 112, D02306, https://doi.org/10.1002/cphc.200500158, 2007.
Zhou, J., Swietlicki, E., Berg, O. H., Aalto, P. P., Hämeri, K., Nilsson, E. D., and Leck, C.: Hygroscopic properties of aerosol particles over the central Arctic Ocean during summer, J. Geophys. Res., 106, 32111–32123, 2001.
Zhou, W., Apkarian, R., Wang, Z. L., and Joy, D.: Fundamentals of scanning electron microscopy, in: Scanning Microscopy for Nanotechnology – Techniques and Applications, edited by: Zhou, W. and Wang, Z. L., Springer Business + Media, New York, 2006.
Short summary
Aerosol particles collected during the ASCOS expedition in the high Arctic in summer 2008 were examined with electron microscopy and elemental dispersive X-ray spectroscopy. The majority of particles consisted of marine gel matter accompanied by minor fractions of ammonium (bi)sulfate and internally mixed sulfur containing particles. Depending on their morphology, marine gel particles showed prevalence for either the ions Na+/K+ or Ca2+/Mg2+.
Aerosol particles collected during the ASCOS expedition in the high Arctic in summer 2008 were...
Altmetrics
Final-revised paper
Preprint