Articles | Volume 20, issue 7
https://doi.org/10.5194/acp-20-4295-2020
© Author(s) 2020. 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-20-4295-2020
© Author(s) 2020. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Research article
| 
09 Apr 2020
Research article |
| 09 Apr 2020
| 09 Apr 2020
Fossil fuel combustion, biomass burning and biogenic sources of fine carbonaceous aerosol in the Carpathian Basin
Institute of Chemistry, Eötvös University, Budapest,
Hungary
Anikó Vasanits-Zsigrai
Institute of Chemistry, Eötvös University, Budapest,
Hungary
Attila Machon
Air Quality Reference Center, Hungarian Meteorological Service,
Budapest, Hungary
Tamás Varga
Isotope Climatology and Environmental Research Centre, Institute for
Nuclear Research, Debrecen, Hungary
István Major
Isotope Climatology and Environmental Research Centre, Institute for
Nuclear Research, Debrecen, Hungary
Virág Gergely
Isotope Climatology and Environmental Research Centre, Institute for
Nuclear Research, Debrecen, Hungary
Mihály Molnár
Isotope Climatology and Environmental Research Centre, Institute for
Nuclear Research, Debrecen, Hungary
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Imre Salma, Wanda Thén, Pasi Aalto, Veli-Matti Kerminen, Anikó Kern, Zoltán Barcza, Tuukka Petäjä, and Markku Kulmala
Atmos. Chem. Phys., 21, 2861–2880, https://doi.org/10.5194/acp-21-2861-2021, https://doi.org/10.5194/acp-21-2861-2021, 2021
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The distribution of the monthly mean nucleation frequency possessed a characteristic pattern. Its shape was compared to those of environmental variables, including vegetation-derived properties. The spring maximum in the occurrence frequency often overlapped with the positive T anomaly. The link between the heat stress and the occurrence minimum in summer could not be proven, whereas an association between the occurrence frequency and vegetation growth dynamics was clearly identified in spring.
András Hoffer, Beatrix Jancsek-Turóczi, Ádám Tóth, Gyula Kiss, Anca Naghiu, Erika Andrea Levei, Luminita Marmureanu, Attila Machon, and András Gelencsér
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Emission factors for PM10 and polycyclic aromatic hydrocarbons (PAHs) are reported for the first time ever for the indoor combustion of 12 common types of municipal solid waste that are frequently burned in households worldwide. We have found that waste burning emits up to 40 times more PM10 and 800 times more PAHs than the combustion of dry firewood. Our finding highlights the need for coordinated actions against illegal waste combustion and the extreme health hazard associated with it.
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Atmospheric aerosols have diverse effects on air quality, human health, and global climate. One important source of aerosols is their formation via nucleation and growth in the atmosphere. We have analyzed long-term observations of regional new particle formation events around the globe and provide a comprehensive view on the characteristics of this phenomenon in diverse environments. The results are useful in developing more realistic representation of atmospheric aerosols in global models.
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Short summary
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The urban aerosol particles in central Budapest consist of two externally mixed classes – nearly hydrophobic and less volatile particles, which were assigned to vehicle emissions (large mass fractions of soot likely coated with water-insoluble organic compounds) – and of less hygroscopic and volatile particles (moderately transformed aged combustion particles composed of partly oxygenated organics and inorganic salts internally mixed).
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Short summary
Short summary
The largest source of ultrafine (UF) aerosol particles in cities seems to be vehicular road traffic. We quantified here that nucleation generates 37 % of UF particles in the near-city background, and 13 % in the city centre. This implies that the health-related consequences of atmospheric new particle formation and growth processes in cities should also be considered in addition to their urban climate implications.
Imre Salma, Zoltán Németh, Tamás Weidinger, Willy Maenhaut, Magda Claeys, Mihály Molnár, István Major, Tibor Ajtai, Noémi Utry, and Zoltán Bozóki
Atmos. Chem. Phys., 17, 13767–13781, https://doi.org/10.5194/acp-17-13767-2017, https://doi.org/10.5194/acp-17-13767-2017, 2017
Short summary
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The major finding of this study lies in the new pragmatic coupled radiocarbon–LVG apportionment scheme, which allows assessment of the contribution of the major carbonaceous species from fossil fuel combustion, biomass burning and biogenic sources with a reasonable uncertainty, and without coupling of thermal or separation methods with an AMS for rather small amounts of samples.
Imre Salma, Zoltán Németh, Veli-Matti Kerminen, Pasi Aalto, Tuomo Nieminen, Tamás Weidinger, Ágnes Molnár, Kornélia Imre, and Markku Kulmala
Atmos. Chem. Phys., 16, 8715–8728, https://doi.org/10.5194/acp-16-8715-2016, https://doi.org/10.5194/acp-16-8715-2016, 2016
Short summary
Short summary
We revealed that NPF seen in a central large city of the Carpathian Basin, Budapest, and its regional background occur in a consistent and spatially coherent way as a result of a joint atmospheric phenomenon taking place on large horizontal scales.
Imre Salma, Zoltán Németh, Tamás Weidinger, Boldizsár Kovács, and Gergely Kristóf
Atmos. Chem. Phys., 16, 7837–7851, https://doi.org/10.5194/acp-16-7837-2016, https://doi.org/10.5194/acp-16-7837-2016, 2016
Z. Németh and I. Salma
Atmos. Chem. Phys., 14, 8841–8848, https://doi.org/10.5194/acp-14-8841-2014, https://doi.org/10.5194/acp-14-8841-2014, 2014
Related subject area
Subject: Aerosols | Research Activity: Field Measurements | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
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Automated compound speciation, cluster analysis, and quantification of organic vapors and aerosols using comprehensive two-dimensional gas chromatography and mass spectrometry
Measurement report: Occurrence of aminiums in PM2.5 during winter in China – aminium outbreak during polluted episodes and potential constraints
Bridging gas and aerosol properties between the northeastern US and Bermuda: analysis of eight transit flights
The behaviour of charged particles (ions) during new particle formation events in urban Leipzig, Germany
Sensitivity of aerosol and cloud properties to coupling strength of marine boundary layer clouds over the northwest Atlantic
Exploring the sources of light-absorbing carbonaceous aerosols by integrating observational and modeling results: insights from Northeast China
Characterization of atmospheric water-soluble brown carbon in the Athabasca Oil Sands Region, Canada
Measurement report: Characteristics of airborne black-carbon-containing particles during the 2021 summer COVID-19 lockdown in a typical Yangtze River Delta city, China
Aerosol optical properties within the atmospheric boundary layer predicted from ground-based observations compared to Raman lidar retrievals during RITA-2021
Hygroscopic growth and activation changed submicron aerosol composition and properties in the North China Plain
Measurement report: Formation of tropospheric brown carbon in a lifting air mass
Vertical variability of aerosol properties and trace gases over a remote marine region: a case study over Bermuda
Differences in aerosol and cloud properties along the central California coast when winds change from northerly to southerly
International airport emissions and their impact on local air quality: chemical speciation of ambient aerosols at Madrid–Barajas Airport during the AVIATOR campaign
The local ship speed reduction effect on black carbon emissions measured at a remote marine station
High-altitude aerosol chemical characterization and source identification: insights from the CALISHTO campaign
Measurement report: Impact of emission control measures on environmental persistent free radicals and reactive oxygen species – a short-term case study in Beijing
Characterizing water solubility of fresh and aged secondary organic aerosol in PM2.5 with the stable carbon isotope technique
Measurement report: Impact of cloud processes on secondary organic aerosols at a forested mountain site in southeastern China
Critical contribution of chemically diverse carbonyl molecules to the oxidative potential of atmospheric aerosols
Seasonal Investigation of Ultrafine Particle Composition in an Eastern Amazonian Rainforest
Measurement report: Vanadium-containing ship exhaust particles detected in and above the marine boundary layer in the remote atmosphere
Diverging trends in aerosol sulfate and nitrate measured in the remote North Atlantic in Barbados are attributed to clean air policies, African smoke, and anthropogenic emissions
Diverse sources and aging change the mixing state and ice nucleation properties of aerosol particles over the western Pacific and Southern Ocean
The water-insoluble organic carbon in PM2.5 of typical Chinese urban areas: light-absorbing properties, potential sources, radiative forcing effects, and a possible light-absorbing continuum
Measurement report: Size-resolved secondary organic aerosol formation modulated by aerosol water uptake in wintertime haze
Observations of high time-resolution and size-resolved aerosol chemical composition and microphyscis in the central Arctic: implications for climate-relevant particle properties
Brown carbon aerosol in rural Germany: sources, chemistry, and diurnal variations
In situ measurement of organic aerosol molecular markers in urban Hong Kong during a summer period: temporal variations and source apportionment
Technical note: Determining chemical composition of atmospheric single particles by a standard-free mass calibration algorithm
Different formation pathways of nitrogen-containing organic compounds in aerosols and fog water in northern China
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.
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.
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.
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.
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.
Pramod Kumar, Khushboo Sharma, Ankita Malu, Rajeev Rajak, Aparna Gupta, Bidyutjyoti Baruah, Shailesh Yadav, Thupstan Angchuk, Jayant Sharma, Rakesh Kumar Ranjan, Anil Kumar Misra, and Nishchal Wanjari
Atmos. Chem. Phys., 24, 11585–11601, https://doi.org/10.5194/acp-24-11585-2024, https://doi.org/10.5194/acp-24-11585-2024, 2024
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This work monitors and assesses air pollution, especially black and brown carbon, its controlling factor, and its effect on the environment of Sikkim Himalayan region. The huge urban sprawl in recent decades has led to regional human-induced air pollution in the region. Black carbon was highest in April 2021 and March 2022, exceeding the WHO limit. The monsoon season causes huge rainfall over the region, which reduces the pollutants by scavenging (rainout and washout).
Maria P. Velásquez-García, K. Santiago Hernández, James A. Vergara-Correa, Richard J. Pope, Miriam Gómez-Marín, and Angela M. Rendón
Atmos. Chem. Phys., 24, 11497–11520, https://doi.org/10.5194/acp-24-11497-2024, https://doi.org/10.5194/acp-24-11497-2024, 2024
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In the Aburrá Valley, northern South America, local emissions determine air quality conditions. However, we found that external sources, such as regional fires, Saharan dust, and volcanic emissions, increase particulate concentrations and worsen chemical composition by introducing elements like heavy metals. Dry winds and source variability contribute to seasonal influences on these events. This study assesses the air quality risks posed by such events, which can affect broad regions worldwide.
Meng Wang, Qiyuan Wang, Steven Sai Hang Ho, Jie Tian, Yong Zhang, Shun-cheng Lee, and Junji Cao
Atmos. Chem. Phys., 24, 11175–11189, https://doi.org/10.5194/acp-24-11175-2024, https://doi.org/10.5194/acp-24-11175-2024, 2024
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We studied nitrogen-containing organic compounds (NOCs) in particulate matter <2.5 µm particles on the southeastern Tibetan Plateau. We found that biomass burning and transboundary transport are the main sources of NOCs in the high-altitude area. Understanding these aerosol sources informs how they add to regional and potentially global climate changes. Our findings could help shape effective environmental policies to enhance air quality and address climate impacts in this sensitive region.
Yi-Jia Ma, Yu Xu, Ting Yang, Lin Gui, Hong-Wei Xiao, Hao Xiao, and Hua-Yun Xiao
EGUsphere, https://doi.org/10.5194/egusphere-2024-2602, https://doi.org/10.5194/egusphere-2024-2602, 2024
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The abundance, potential precursors, and main formation mechanisms of NOCs in PM2.5 during winter were compared among cities with different energy consumption. We found that the aerosol NOC pollution during winter is closely associated with the intensity of precursor emissions and the efficiency of aqueous-phase processes in converting these emissions into NOCs. The overall results highlight the importance of emission reduction strategies in controlling aerosol NOCs pollution during winter.
Jinbo Wang, Jiaping Wang, Yuxuan Zhang, Tengyu Liu, Xuguang Chi, Xin Huang, Dafeng Ge, Shiyi Lai, Caijun Zhu, Lei Wang, Qiaozhi Zha, Ximeng Qi, Wei Nie, Congbin Fu, and Aijun Ding
Atmos. Chem. Phys., 24, 11063–11080, https://doi.org/10.5194/acp-24-11063-2024, https://doi.org/10.5194/acp-24-11063-2024, 2024
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In this study, we found large spatial discrepancies in the physical and chemical properties of black carbon over the Tibetan Plateau (TP). Elevated anthropogenic emissions from low-altitude regions can significantly change the mass concentration, mixing state and chemical composition of black-carbon-containing aerosol in the TP region, further altering its light absorption ability. Our study emphasizes the vulnerability of remote plateau regions to intense anthropogenic influences.
Liyuan Zhou, Qianyun Liu, Christian M. Salvador, Michael Le Breton, Mattias Hallquist, Jian Zhen Yu, Chak K. Chan, and Åsa M. Hallquist
Atmos. Chem. Phys., 24, 11045–11061, https://doi.org/10.5194/acp-24-11045-2024, https://doi.org/10.5194/acp-24-11045-2024, 2024
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Our research on city bus emissions reveals that alternative fuels (compressed natural gas and biofuels) reduce fresh particle emissions compared to diesel. However, all fuels lead to secondary air pollution. Aiming at guiding better environmental policies, we studied 76 buses using advanced emission measurement techniques. This work sheds light on the complex effects of bus fuels on urban air quality, emphasizing the need for comprehensive evaluations of future transportation technologies.
Xu Yang, Fobang Liu, Shuqi Yang, Yuling Yang, Yanan Wang, Jingjing Li, Mingyu Zhao, Zhao Wang, Kai Wang, Chi He, and Haijie Tong
Atmos. Chem. Phys., 24, 11029–11043, https://doi.org/10.5194/acp-24-11029-2024, https://doi.org/10.5194/acp-24-11029-2024, 2024
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A study in the rural North China Plain showed environmentally persistent free radicals (EPFRs) in atmospheric particulate matter (PM), with a notable water-soluble fraction likely from atmospheric oxidation during transport. Significant positive correlations between EPFRs and the water-soluble oxidative potential of PM2.5 were found, primarily attributable to the water-soluble fractions of EPFRs. These findings emphasize understanding EPFRs' atmospheric evolution for climate and health impacts.
Kirsten N. Fossum, Chunshui Lin, Niall O'Sullivan, Lu Lei, Stig Hellebust, Darius Ceburnis, Aqeel Afzal, Anja Tremper, David Green, Srishti Jain, Steigvilė Byčenkienė, Colin O'Dowd, John Wenger, and Jurgita Ovadnevaite
Atmos. Chem. Phys., 24, 10815–10831, https://doi.org/10.5194/acp-24-10815-2024, https://doi.org/10.5194/acp-24-10815-2024, 2024
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The chemical composition and sources of submicron aerosol in the Dublin Port area were investigated over a month-long campaign. Two distinct types of ship emissions were identified and characterised: sulfate-rich plumes from the use of heavy fuel oil with scrubbers and organic-rich plumes from the use of low-sulfur fuels. The latter were more frequent, emitting double the particle number and having a typical V / Ni ratio for ship emission.
Xiao He, Xuan Zheng, Shuwen Guo, Lewei Zeng, Ting Chen, Bohan Yang, Shupei Xiao, Qiongqiong Wang, Zhiyuan Li, Yan You, Shaojun Zhang, and Ye Wu
Atmos. Chem. Phys., 24, 10655–10666, https://doi.org/10.5194/acp-24-10655-2024, https://doi.org/10.5194/acp-24-10655-2024, 2024
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This study introduces an innovative method for identifying and quantifying complex organic vapors and aerosols. By combining advanced analytical techniques and new algorithms, we categorized thousands of compounds from heavy-duty diesel vehicles and ambient air and highlighted specific tracers for emission sources. The innovative approach enhances peak identification, reduces quantification uncertainties, and offers new insights for air quality management and atmospheric chemistry.
Yu Xu, Tang Liu, Yi-Jia Ma, Qi-Bin Sun, Hong-Wei Xiao, Hao Xiao, Hua-Yun Xiao, and Cong-Qiang Liu
Atmos. Chem. Phys., 24, 10531–10542, https://doi.org/10.5194/acp-24-10531-2024, https://doi.org/10.5194/acp-24-10531-2024, 2024
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This study investigates the characteristics of aminiums and ammonium in PM2.5 on clean and polluted winter days in 11 Chinese cities, highlighting the possibility of the competitive uptake of ammonia versus amines on acidic aerosols or the displacement of aminiums by ammonia under high-ammonia conditions. The overall results deepen the understanding of the spatiotemporal differences in aminium characteristics and formation in China.
Cassidy Soloff, Taiwo Ajayi, Yonghoon Choi, Ewan C. Crosbie, Joshua P. DiGangi, Glenn S. Diskin, Marta A. Fenn, Richard A. Ferrare, Francesca Gallo, Johnathan W. Hair, Miguel Ricardo A. Hilario, Simon Kirschler, Richard H. Moore, Taylor J. Shingler, Michael A. Shook, Kenneth L. Thornhill, Christiane Voigt, Edward L. Winstead, Luke D. Ziemba, and Armin Sorooshian
Atmos. Chem. Phys., 24, 10385–10408, https://doi.org/10.5194/acp-24-10385-2024, https://doi.org/10.5194/acp-24-10385-2024, 2024
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Using aircraft measurements over the northwestern Atlantic between the US East Coast and Bermuda and trajectory modeling of continental outflow, we identify trace gas and particle properties that exhibit gradients with offshore distance and quantify these changes with high-resolution measurements of concentrations and particle chemistry, size, and scattering properties. This work furthers our understanding of the complex interactions between continental and marine environments.
Alex Rowell, James Brean, David C. S. Beddows, Zongbo Shi, Avinash Kumar, Matti Rissanen, Miikka Dal Maso, Peter Mettke, Kay Weinhold, Maik Merkel, and Roy M. Harrison
Atmos. Chem. Phys., 24, 10349–10361, https://doi.org/10.5194/acp-24-10349-2024, https://doi.org/10.5194/acp-24-10349-2024, 2024
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Ions enhance the formation and growth rates of new particles, affecting the Earth's radiation budget. Despite these effects, there is little published data exploring the sources of ions in the urban environment and their role in new particle formation (NPF). Here we show that natural ion sources dominate in urban environments, while traffic is a secondary source. Ions contribute up to 12.7 % of the formation rate of particles, indicating that they are important for forming urban PM.
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
EGUsphere, https://doi.org/10.5194/egusphere-2024-2743, https://doi.org/10.5194/egusphere-2024-2743, 2024
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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.
Yuan Cheng, Xu-bing Cao, Sheng-qiang Zhu, Zhi-qing Zhang, Jiu-meng Liu, Hong-liang Zhang, Qiang Zhang, and Ke-bin He
Atmos. Chem. Phys., 24, 9869–9883, https://doi.org/10.5194/acp-24-9869-2024, https://doi.org/10.5194/acp-24-9869-2024, 2024
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The agreement between observational and modeling results is essential for the development of efficient air pollution control strategies. Here we constrained the modeling results of carbonaceous aerosols by field observation in Northeast China, a historically overlooked but recently targeted region of national clean-air actions. Our study suggested that the simulation of agricultural fire emissions and secondary organic aerosols remains challenging.
Dane Blanchard, Mark Gordon, Duc Huy Dang, Paul Andrew Makar, and Julian Aherne
EGUsphere, https://doi.org/10.5194/egusphere-2024-2584, https://doi.org/10.5194/egusphere-2024-2584, 2024
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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 (summer 2021) found that oil sands operations were a measurable source of brown carbon. Industrial aerosol emissions may impact atmospheric reaction chemistry and albedo. These findings demonstrate that fluorescence spectroscopy can be applied to monitor brown carbon in the ASOR.
Yuan Dai, Junfeng Wang, Houjun Wang, Shijie Cui, Yunjiang Zhang, Haiwei Li, Yun Wu, Ming Wang, Eleonora Aruffo, and Xinlei Ge
Atmos. Chem. Phys., 24, 9733–9748, https://doi.org/10.5194/acp-24-9733-2024, https://doi.org/10.5194/acp-24-9733-2024, 2024
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Short-term strict emission control can improve air quality, but its effectiveness needs assessment. During the 2021 summer COVID-19 lockdown in Yangzhou, we found that PM2.5 levels did not decrease despite reduced primary emissions. Aged black-carbon particles increased substantially due to higher O3 levels and transported pollutants. High humidity and low wind also played key roles. The results highlight the importance of a regionally balanced control strategy for future air quality management.
Xinya Liu, Diego Alves Gouveia, Bas Henzing, Arnoud Apituley, Arjan Hensen, Danielle van Dinther, Rujin Huang, and Ulrike Dusek
Atmos. Chem. Phys., 24, 9597–9614, https://doi.org/10.5194/acp-24-9597-2024, https://doi.org/10.5194/acp-24-9597-2024, 2024
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The vertical distribution of aerosol optical properties is important for their effect on climate. This is usually measured by lidar, which has limitations, most notably the assumption of a lidar ratio. Our study shows that routine surface-level aerosol measurements are able to predict this lidar ratio reasonably well within the lower layers of the atmosphere and thus provide a relatively simple and cost-effective method to improve lidar measurements.
Weiqi Xu, Ye Kuang, Wanyun Xu, Zhiqiang Zhang, Biao Luo, Xiaoyi Zhang, Jiangchuang Tao, Hongqin Qiao, Li Liu, and Yele Sun
Atmos. Chem. Phys., 24, 9387–9399, https://doi.org/10.5194/acp-24-9387-2024, https://doi.org/10.5194/acp-24-9387-2024, 2024
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We deployed an advanced aerosol–fog sampling system at a rural site in the North China Plain to investigate impacts of aerosol hygroscopic growth and activation on the physicochemical properties of submicron aerosols. Observed results highlighted remarkably different aqueous processing of primary and secondary submicron aerosol components under distinct ambient relative humidity (RH) conditions and that RH levels significantly impact aerosol sampling through the aerosol swelling effect.
Can Wu, Xiaodi Liu, Ke Zhang, Si Zhang, Cong Cao, Jianjun Li, Rui Li, Fan Zhang, and Gehui Wang
Atmos. Chem. Phys., 24, 9263–9275, https://doi.org/10.5194/acp-24-9263-2024, https://doi.org/10.5194/acp-24-9263-2024, 2024
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Brown carbon (BrC) is prevalent in the troposphere and can efficiently absorb solar and terrestrial radiation. Our observations show that the enhanced light absorption of BrC relative to black carbon at the tropopause can be attributed to the formation of nitrogen-containing organic compounds through the aqueous-phase reactions of carbonyls with ammonium.
Taiwo Ajayi, Yonghoon Choi, Ewan C. Crosbie, Joshua P. DiGangi, Glenn S. Diskin, Marta A. Fenn, Richard A. Ferrare, Johnathan W. Hair, Miguel Ricardo A. Hilario, Chris A. Hostetler, Simon Kirschler, Richard H. Moore, Taylor J. Shingler, Michael A. Shook, Cassidy Soloff, Kenneth L. Thornhill, Christiane Voigt, Edward L. Winstead, Luke D. Ziemba, and Armin Sorooshian
Atmos. Chem. Phys., 24, 9197–9218, https://doi.org/10.5194/acp-24-9197-2024, https://doi.org/10.5194/acp-24-9197-2024, 2024
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This study uses airborne data to examine vertical profiles of trace gases, aerosol particles, and meteorological variables over a remote marine area (Bermuda). Results show distinct differences based on both air mass source region (North America, Ocean, Caribbean/North Africa) and altitude for a given air mass type. This work highlights the sensitivity of remote marine areas to long-range transport and the importance of considering the vertical dependence of trace gas and aerosol properties.
Kira Zeider, Grace Betito, Anthony Bucholtz, Peng Xian, Annette Walker, and Armin Sorooshian
Atmos. Chem. Phys., 24, 9059–9083, https://doi.org/10.5194/acp-24-9059-2024, https://doi.org/10.5194/acp-24-9059-2024, 2024
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The predominant wind direction along the California coast (northerly) reverses several times during the summer (to southerly). The effects of these wind reversals on aerosol and cloud characteristics are not well understood. Using data from multiple datasets we found that southerly flow periods had enhanced signatures of anthropogenic emissions due to shipping and continental sources, and clouds had more but smaller droplets.
Saleh Alzahrani, Doğuşhan Kılıç, Michael Flynn, Paul I. Williams, and James Allan
Atmos. Chem. Phys., 24, 9045–9058, https://doi.org/10.5194/acp-24-9045-2024, https://doi.org/10.5194/acp-24-9045-2024, 2024
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This paper investigates emissions from aviation activities at an international airport to evaluate their impact on local air quality. The study provides detailed insights into the chemical composition of aerosols and key pollutants in the airport environment. Source apportionment analysis using positive matrix factorisation (PMF) identified three significant sources: less oxidised oxygenated organic aerosol, alkane organic aerosol, and more oxidised oxygenated organic aerosol.
Mikko Heikkilä, Krista Luoma, Timo Mäkelä, and Tiia Grönholm
Atmos. Chem. Phys., 24, 8927–8941, https://doi.org/10.5194/acp-24-8927-2024, https://doi.org/10.5194/acp-24-8927-2024, 2024
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Black carbon (BC) concentration was measured from 211 ship exhaust gas plumes at a remote marine station. Emission factors of BC were calculated in grams per kilogram of fuel. Ships with an exhaust gas cleaning system (EGCS) were found to have median BC emissions per fuel consumed 5 times lower than ships without an EGCS. However, this might be because of non-EGCS ships running at low engine loads rather than the EGCS itself. A local speed restriction would increase BC emissions of ships.
Olga Zografou, Maria Gini, Prodromos Fetfatzis, Konstantinos Granakis, Romanos Foskinis, Manousos Ioannis Manousakas, Fotios Tsopelas, Evangelia Diapouli, Eleni Dovrou, Christina N. Vasilakopoulou, Alexandros Papayannis, Spyros N. Pandis, Athanasios Nenes, and Konstantinos Eleftheriadis
Atmos. Chem. Phys., 24, 8911–8926, https://doi.org/10.5194/acp-24-8911-2024, https://doi.org/10.5194/acp-24-8911-2024, 2024
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Characterization of PM1 and positive matrix factorization (PMF) source apportionment of organic and inorganic fractions were conducted at the high-altitude station (HAC)2. Cloud presence reduced PM1, affecting sulfate more than organics. Free-troposphere (FT) conditions showed more black carbon (eBC) than planetary boundary layer (PBL) conditions.
Yuanyuan Qin, Xinghua Zhang, Wei Huang, Juanjuan Qin, Xiaoyu Hu, Yuxuan Cao, Tianyi Zhao, Yang Zhang, Jihua Tan, Ziyin Zhang, Xinming Wang, and Zhenzhen Wang
Atmos. Chem. Phys., 24, 8737–8750, https://doi.org/10.5194/acp-24-8737-2024, https://doi.org/10.5194/acp-24-8737-2024, 2024
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Environmental persistent free radicals (EPFRs) and reactive oxygen species (ROSs) play an active role in the atmosphere. Despite control measures having effectively reduced their emissions, reductions were less than in PM2.5. Emission control measures performed well in achieving Parade Blue, but reducing the impact of the atmosphere on human health remains challenging. Thus, there is a need to reassess emission control measures to better address the challenges posed by EPFRs and ROSs.
Fenghua Wei, Xing Peng, Liming Cao, Mengxue Tang, Ning Feng, Xiaofeng Huang, and Lingyan He
Atmos. Chem. Phys., 24, 8507–8518, https://doi.org/10.5194/acp-24-8507-2024, https://doi.org/10.5194/acp-24-8507-2024, 2024
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The water solubility of secondary organic aerosols (SOAs) is a crucial factor in determining their hygroscopicity and climatic impact. Stable carbon isotope and mass spectrometry techniques were combined to assess the water solubility of SOAs with different aging degrees in a coastal megacity in China. This work revealed a much higher water-soluble fraction of aged SOA compared to fresh SOA, indicating that the aging degree of SOA has considerable impacts on its water solubility.
Zijun Zhang, Weiqi Xu, Yi Zhang, Wei Zhou, Xiangyu Xu, Aodong Du, Yinzhou Zhang, Hongqin Qiao, Ye Kuang, Xiaole Pan, Zifa Wang, Xueling Cheng, Lanzhong Liu, Qingyan Fu, Douglas R. Worsnop, Jie Li, and Yele Sun
Atmos. Chem. Phys., 24, 8473–8488, https://doi.org/10.5194/acp-24-8473-2024, https://doi.org/10.5194/acp-24-8473-2024, 2024
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We investigated aerosol composition and sources and the interaction between secondary organic aerosol (SOA) and clouds at a regional mountain site in southeastern China. Clouds efficiently scavenge more oxidized SOA; however, cloud evaporation leads to the production of less oxidized SOA. The unexpectedly high presence of nitrate in aerosol particles indicates that nitrate formed in polluted areas has undergone interactions with clouds, significantly influencing the regional background site.
Feifei Li, Shanshan Tang, Jitao Lv, Shiyang Yu, Xu Sun, Dong Cao, Yawei Wang, and Guibin Jiang
Atmos. Chem. Phys., 24, 8397–8411, https://doi.org/10.5194/acp-24-8397-2024, https://doi.org/10.5194/acp-24-8397-2024, 2024
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Targeted derivatization and non-targeted analysis with Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) were used to reveal the molecular composition of carbonyl molecules in PM2.5, and the important role of carbonyls in increasing the oxidative potential of organic aerosol was found in real samples.
Adam E. Thomas, Hayley S. Glicker, Alex B. Guenther, Roger Seco, Oscar Vega Bustillos, Julio Tota, Rodrigo A. F. Souza, and James N. Smith
EGUsphere, https://doi.org/10.5194/egusphere-2024-2230, https://doi.org/10.5194/egusphere-2024-2230, 2024
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We present measurements of the composition of ultrafine particles collected from the eastern Amazon, a relatively understudied region that is subjected to increasing human influence. We find that while isoprene chemistry is likely significant to ultrafine particle growth throughout the year, compounds related to other sources such as biological spore emissions and biomass burning exhibit striking seasonal differences, implying an extensive variation in regional ultrafine particle sources.
Maya Abou-Ghanem, Daniel M. Murphy, Gregory P. Schill, Michael J. Lawler, and Karl D. Froyd
Atmos. Chem. Phys., 24, 8263–8275, https://doi.org/10.5194/acp-24-8263-2024, https://doi.org/10.5194/acp-24-8263-2024, 2024
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Using particle analysis by laser mass spectrometry, we examine vanadium-containing ship exhaust particles measured on NASA's DC-8 during the Atmospheric Tomography Mission (ATom). Our results reveal ship exhaust particles are sufficiently widespread in the marine atmosphere and experience atmospheric aging. Finally, we use laboratory calibrations to determine the vanadium, sulfate, and organic single-particle mass fractions of vanadium-containing ship exhaust particles.
Cassandra J. Gaston, Joseph M. Prospero, Kristen Foley, Havala O. T. Pye, Lillian Custals, Edmund Blades, Peter Sealy, and James A. Christie
Atmos. Chem. Phys., 24, 8049–8066, https://doi.org/10.5194/acp-24-8049-2024, https://doi.org/10.5194/acp-24-8049-2024, 2024
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To understand how changing emissions have impacted aerosols in remote regions, we measured nitrate and sulfate in Barbados and compared them to model predictions from EPA’s Air QUAlity TimE Series (EQUATES). Nitrate was stable, except for spikes in 2008 and 2010 due to transported smoke. Sulfate decreased in the 1990s due to reductions in sulfur dioxide (SO2) in the US and Europe; then it increased in the 2000s, likely due to anthropogenic emissions from Africa.
Jiao Xue, Tian Zhang, Keyhong Park, Jinpei Yan, Young Jun Yoon, Jiyeon Park, and Bingbing Wang
Atmos. Chem. Phys., 24, 7731–7754, https://doi.org/10.5194/acp-24-7731-2024, https://doi.org/10.5194/acp-24-7731-2024, 2024
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Ice formation by particles is an important way of making mixed-phase and ice clouds. We found that particles collected in the marine atmosphere exhibit diverse ice nucleation abilities and mixing states. Sea salt mixed-sulfate particles were enriched in ice-nucleating particles. Selective aging on sea salt particles made particle populations more externally mixed. Characterizations of particles and their mixing state are needed for a better understanding of aerosol–cloud interactions.
Yangzhi Mo, Jun Li, Guangcai Zhong, Sanyuan Zhu, Shizhen Zhao, Jiao Tang, Hongxing Jiang, Zhineng Cheng, Chongguo Tian, Yingjun Chen, and Gan Zhang
Atmos. Chem. Phys., 24, 7755–7772, https://doi.org/10.5194/acp-24-7755-2024, https://doi.org/10.5194/acp-24-7755-2024, 2024
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In this study, we found that biomass burning (31.0 %) and coal combustion (31.1 %) were the dominant sources of water-insoluble organic carbon in China, with coal combustion sources exhibiting the strongest light-absorbing capacity. Additionally, we propose a light-absorbing carbonaceous continuum, revealing that components enriched with fossil sources tend to have stronger light-absorbing capacity, higher aromaticity, higher molecular weights, and greater recalcitrance in the atmosphere.
Jing Duan, Ru-Jin Huang, Ying Wang, Wei Xu, Haobin Zhong, Chunshui Lin, Wei Huang, Yifang Gu, Jurgita Ovadnevaite, Darius Ceburnis, and Colin O'Dowd
Atmos. Chem. Phys., 24, 7687–7698, https://doi.org/10.5194/acp-24-7687-2024, https://doi.org/10.5194/acp-24-7687-2024, 2024
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The chemical composition of atmospheric particles has shown significant changes in recent years. We investigated the potential effects of changes in inorganics on aerosol water uptake and, thus, secondary organic aerosol formation in wintertime haze based on the size-resolved measurements of non-refractory fine particulate matter (NR-PM2.5) in Xi’an, northwestern China. We highlight the key role of aerosol water as a medium to link inorganics and organics in their multiphase processes.
Benjamin Heutte, Nora Bergner, Hélène Angot, Jakob B. Pernov, Lubna Dada, Jessica A. Mirrielees, Ivo Beck, Andrea Baccarini, Matthew Boyer, Jessie M. Creamean, Kaspar R. Daellenbach, Imad El Haddad, Markus M. Frey, Silvia Henning, Tiaa Laurila, Vaios Moschos, Tuukka Petäjä, Kerri A. Pratt, Lauriane L. J. Quéléver, Matthew D. Shupe, Paul Zieger, Tuija Jokinen, and Julia Schmale
EGUsphere, https://doi.org/10.5194/egusphere-2024-1912, https://doi.org/10.5194/egusphere-2024-1912, 2024
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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. Locally wind-generated particles are shown to be an important source of cloud seeds, especially in autumn.
Feng Jiang, Harald Saathoff, Junwei Song, Hengheng Zhang, Linyu Gao, and Thomas Leisner
EGUsphere, https://doi.org/10.5194/egusphere-2024-1848, https://doi.org/10.5194/egusphere-2024-1848, 2024
Short summary
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The chemical composition of brown carbon in the particle and gas phase were 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 rural location in central Europe.
Hongyong Li, Xiaopu Lyu, Likun Xue, Yunxi Huo, Dawen Yao, Haoxian Lu, and Hai Guo
Atmos. Chem. Phys., 24, 7085–7100, https://doi.org/10.5194/acp-24-7085-2024, https://doi.org/10.5194/acp-24-7085-2024, 2024
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Organic aerosol is ubiquitous in the atmosphere and largely explains the gap between current levels of fine particulate matter in many cities and the World Health Organization guideline values. This study highlights the dominant contributions of cooking emissions to organic aerosol when marine air prevailed in Hong Kong, which were occasionally overwhelmed by aromatics-derived secondary organic aerosol in continental ouflows.
Shao Shi, Jinghao Zhai, Xin Yang, Yechun Ruan, Yuanlong Huang, Xujian Chen, Antai Zhang, Jianhuai Ye, Guomao Zheng, Baohua Cai, Yaling Zeng, Yixiang Wang, Chunbo Xing, Yujie Zhang, Tzung-May Fu, Lei Zhu, Huizhong Shen, and Chen Wang
Atmos. Chem. Phys., 24, 7001–7012, https://doi.org/10.5194/acp-24-7001-2024, https://doi.org/10.5194/acp-24-7001-2024, 2024
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The determination of ions in the mass spectra of individual particles remains uncertain. We have developed a standard-free mass calibration algorithm applicable to more than 98 % of ambient particles. With our algorithm, ions with ~ 0.05 Th mass difference could be determined. Therefore, many more atmospheric species could be determined and involved in the source apportionment of aerosols, the study of chemical reaction mechanisms, and the analysis of single-particle mixing states.
Wei Sun, Xiaodong Hu, Yuzhen Fu, Guohua Zhang, Yujiao Zhu, Xinfeng Wang, Caiqing Yan, Likun Xue, He Meng, Bin Jiang, Yuhong Liao, Xinming Wang, Ping'an Peng, and Xinhui Bi
Atmos. Chem. Phys., 24, 6987–6999, https://doi.org/10.5194/acp-24-6987-2024, https://doi.org/10.5194/acp-24-6987-2024, 2024
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The formation pathways of nitrogen-containing compounds (NOCs) in the atmosphere remain unclear. We investigated the composition of aerosols and fog water by state-of-the-art mass spectrometry and compared the formation pathways of NOCs. We found that NOCs in aerosols were mainly formed through nitration reaction, while ammonia addition played a more important role in fog water. The results deepen our understanding of the processes of organic particulate pollution.
Cited articles
Andreae, M. O. and Gelencsér, A.: Black carbon or brown carbon? The nature of light-absorbing carbonaceous aerosols, Atmos. Chem. Phys., 6, 3131–3148, https://doi.org/10.5194/acp-6-3131-2006, 2006.
Andreae, M. O. and Rosenfeld, D.: Aerosol-cloud-precipitation interactions.
Part 1. The nature and sources of cloud-active aerosols, Earth-Sci. Rev.,
89, 13–41, 2008.
Artaxo, P., Rizzo, L. V., Paixao, M., de Lucca, S., Oliveira, P. H., Lara,
L. L., Wiedemann, K. T., Andreae, M. O., Holben, B., Schafer, J., Correia,
A. L., and Pauliquevis, T. M.: Aerosol particles in Amazonia: Their
composition, role in the radiation balance, cloud formation, and nutrient
cycles, in: Amazonia and Global Change, edited by: Keller, M., Bustamante,
M., Gash, J., and Dias, P. S., 233–250, Geophysical Monograph Series, AGU, Washington, DC,
2009.
Bernardoni, V., Vecchi, R., Valli, G., Piazzalunga, A., and Fermo, P.:
PM10 source apportionment in Milan (Italy) using time-resolved data,
Sci. Total Environ., 409, 4788–4795, 2011.
Bernardoni, V., Calzolai, G., Chiari, M., Fedi, M., Lucarelli, F., Nava, S.,
Piazzalunga, A., Riccobono, F., Taccetti, F., Valli, G., and Vecchi, R.:
Radiocarbon analysis on organic and elemental carbon in aerosol samples and
source apportionment at an urban site in Northern Italy, J. Aerosol Sci.,
56, 88–99, 2013.
Birch, M. E. and Cary, R. A.: Elemental carbon-based method for monitoring
occupational exposures to particulate diesel exhaust, Aerosol Sci. Tech.,
25, 221–241, 1996.
Blumberger, Z. I., Vasanits-Zsigrai, A., Farkas, G., and Salma, I.: Mass
size distribution of major monosaccharide anhydrides and mass contribution
of biomass burning, Atmos. Res., 220, 1–9, 2019.
Bonazza, A., Sabbioni, C., and Ghedini, N.: Quantitative data on carbon
fractions in interpretation of black crusts and soiling on European built
heritage, Atmos. Environ., 39, 2607–2618, 2005.
Bonvalot, L., Tuna, T., Fagault, Y., Jaffrezo, J.-L., Jacob, V., Chevrier, F., and Bard, E.: Estimating contributions from biomass burning, fossil fuel combustion, and biogenic carbon to carbonaceous aerosols in the Valley of Chamonix: a dual approach based on radiocarbon and levoglucosan, Atmos. Chem. Phys., 16, 13753–13772, https://doi.org/10.5194/acp-16-13753-2016, 2016.
Burnett, R., Chen, H., Szyszkowicz, M., Fann, N., Hubbell, B., Pope, C. A.,
Apte, J. S., Brauer, M., Cohen, A., Weichenthal, S., Coggins, J., Di, Q.,
Brunekreef, B., Frostad, J., Lim, S. S., Kan, H., Walker, K. D., Thurston,
G. D., Hayes, R. B., Lim, C. C., Turner, M. C., Jerrett, M., Krewski, D.,
Gapstur, S. M., Diver, W. R., Ostro, B., Goldberg, D., Crouse, D. L.,
Martin, R. V., Peters, P., Pinault, L., Tjepkema, M., van Donkelaar, A.,
Villeneuve, P. J., Miller, A. B., Yin, P., Zhou, M., Wang, L., Janssen, N.
A. H., Marra, M., Atkinson, R. W., Tsang, H., Quoc Thach, T., Cannon, J. B.,
Allen, R. T., Hart, J. E., Laden, F., Cesaroni, G., Forastiere, F.,
Weinmayr, G., Jaensch, A., Nagel, G., Concin, H., and Spadaro, J. V.: Global
estimates of mortality associated with long-term exposure to outdoor fine
particulate matter, P. Natl. Acad. Sci. USA, 115, 9592–9597, 2018.
Burr, G. S. and Jull, A. J. T.: Accelerator mass spectrometry for
radiocarbon research, in: Encyclopedia of mass spectrometry, edited by: Gross, M. L.
and Caprioli, R., Elsevier, Amsterdam, 2009.
Caseiro, A., Bauer, H., Schmidl, C., Pio, C. A., and Puxbaum, H.: Wood
burning impact on PM10 in three Austrian regions, Atmos. Environ., 43,
2186–2195, 2009.
Cecchini, M. A., Machado, L. A. T., Andreae, M. O., Martin, S. T., Albrecht, R. I., Artaxo, P., Barbosa, H. M. J., Borrmann, S., Fütterer, D., Jurkat, T., Mahnke, C., Minikin, A., Molleker, S., Pöhlker, M. L., Pöschl, U., Rosenfeld, D., Voigt, C., Weinzierl, B., and Wendisch, M.: Sensitivities of Amazonian clouds to aerosols and updraft speed, Atmos. Chem. Phys., 17, 10037–10050, https://doi.org/10.5194/acp-17-10037-2017, 2017.
Chen, J., Li, Ch., Ristovski, Z., Milic, A., Gu, Y., Islam, M. S., Wang, S.,
Hao, J., Zhang, H., He, C., Guo, H., Fu, H., Miljevic, B., Morawska, L.,
Thai, P., Lam, Y. F., Pereira, G., Ding, A., Huang, X., and Dumka, U. C.: A
review of biomass burning: Emissions and impacts on air quality, health and
climate in China, Sci. Total Environ., 579, 1000–1034, 2017.
Cirino, G. G., Souza, R. A. F., Adams, D. K., and Artaxo, P.: The effect of atmospheric aerosol particles and clouds on net ecosystem exchange in the Amazon, Atmos. Chem. Phys., 14, 6523–6543, https://doi.org/10.5194/acp-14-6523-2014, 2014.
Claeys, M., Kourtchev, I., Pashynska, V., Vas, G., Vermeylen, R., Wang, W., Cafmeyer, J., Chi, X., Artaxo, P., Andreae, M. O., and Maenhaut, W.: Polar organic marker compounds in atmospheric aerosols during the LBA-SMOCC 2002 biomass burning experiment in Rondônia, Brazil: sources and source processes, time series, diel variations and size distributions, Atmos. Chem. Phys., 10, 9319–9331, https://doi.org/10.5194/acp-10-9319-2010, 2010.
Fabbri, D., Torri, C., Simoneit, B. R. T., Marynowski, L., Rushdi, A. I.,
and Fabiańska, M. J.: Levoglucosan and other cellulose and lignin
markers in emissions from burning of Miocene lignites, Atmos. Environ., 43,
2286–2295, 2009.
Favez, O., El Haddad, I., Piot, C., Boréave, A., Abidi, E., Marchand, N., Jaffrezo, J.-L., Besombes, J.-L., Personnaz, M.-B., Sciare, J., Wortham, H., George, C., and D'Anna, B.: Inter-comparison of source apportionment models for the estimation of wood burning aerosols during wintertime in an Alpine city (Grenoble, France), Atmos. Chem. Phys., 10, 5295–5314, https://doi.org/10.5194/acp-10-5295-2010, 2010.
Fine, P. M., Cass, G. R., and Simoneit, B. R. T.: Chemical characterization
of fine particle emissions from the fireplace combustion of wood types grown
in the Midwestern and Western United States, Environ. Eng. Sci., 21,
387–409, 2004.
Forello, A. C., Bernardoni, V., Calzolai, G., Lucarelli, F., Massabò, D., Nava, S., Pileci, R. E., Prati, P., Valentini, S., Valli, G., and Vecchi, R.: Exploiting multi-wavelength aerosol absorption coefficients in a multi-time resolution source apportionment study to retrieve source-dependent absorption parameters, Atmos. Chem. Phys., 19, 11235–11252, https://doi.org/10.5194/acp-19-11235-2019, 2019.
Fraser, M. P. and Lakshmanan, K.: Using levoglucosan as a molecular marker
for the long range transport of biomass combustion aerosols, Environ. Sci.
Technol., 34, 4560–4564, 2000.
Fuzzi, S., Baltensperger, U., Carslaw, K., Decesari, S., Denier van der Gon, H., Facchini, M. C., Fowler, D., Koren, I., Langford, B., Lohmann, U., Nemitz, E., Pandis, S., Riipinen, I., Rudich, Y., Schaap, M., Slowik, J. G., Spracklen, D. V., Vignati, E., Wild, M., Williams, M., and Gilardoni, S.: Particulate matter, air quality and climate: lessons learned and future needs, Atmos. Chem. Phys., 15, 8217–8299, https://doi.org/10.5194/acp-15-8217-2015, 2015.
Gelencsér, A., May, B., Simpson, D., Sánchez-Ochoa, A.,
Kasper-Giebl, A., Puxbaum, H., Caseiro, A., Pio, C., and Legrand, M.: Source
apportionment of PM2.5 organic aerosol over Europe: primary/secondary,
natural/anthropogenic, and fossil/biogenic origin, J. Geophys. Res., 112,
D23S04, https://doi.org/10.1029/2006JD008094, 2007.
Hallquist, M., Wenger, J. C., Baltensperger, U., Rudich, Y., Simpson, D., Claeys, M., Dommen, J., Donahue, N. M., George, C., Goldstein, A. H., Hamilton, J. F., Herrmann, H., Hoffmann, T., Iinuma, Y., Jang, M., Jenkin, M. E., Jimenez, J. L., Kiendler-Scharr, A., Maenhaut, W., McFiggans, G., Mentel, Th. F., Monod, A., Prévôt, A. S. H., Seinfeld, J. H., Surratt, J. D., Szmigielski, R., and Wildt, J.: The formation, properties and impact of secondary organic aerosol: current and emerging issues, Atmos. Chem. Phys., 9, 5155–5236, https://doi.org/10.5194/acp-9-5155-2009, 2009.
Hays, M. D., Smith, N. D., Kinsey, J., Dong, Y., and Kariher, P.: Polycyclic
aromatic hydrocarbon size distributions in aerosols from appliances of
residential wood combustion as determined by direct thermal
desorption-GC/MS, J. Aerosol Sci., 34, 1061–1084, 2003.
Heal, M. R., Naysmith, Ph., Cook, G. T. Xu, S., Duran, T. R., and Harrison,
R. M.: Application of 14C analyses to source apportionment of
carbonaceous PM2.5 in the UK, Atmos. Environ., 45, 2341–2348, 2011.
Hennigan, C. J., Sullivan, A. P., Collett Jr., J. L., and Robinson, A. L.:
Levoglucosan stability in biomass burning particles exposed to hydroxyl
radicals, Geophys. Res. Lett., 37, L09806, https://doi.org/10.1029/2010GL043088, 2010.
Hoffmann, D., Tilgner, A., Iinuma, Y., and Herrmann, H.: Atmospheric
stability of levoglucosan: A detailed laboratory and modelling study,
Environ. Sci. Technol., 44, 694–699, 2010.
Hopke, Ph. K.: Review of receptor modeling methods for source apportionment,
J. Air Waste Manage., 66, 237–259, 2016.
Hoyle, C. R., Boy, M., Donahue, N. M., Fry, J. L., Glasius, M., Guenther, A., Hallar, A. G., Huff Hartz, K., Petters, M. D., Petäjä, T., Rosenoern, T., and Sullivan, A. P.: A review of the anthropogenic influence on biogenic secondary organic aerosol, Atmos. Chem. Phys., 11, 321–343, https://doi.org/10.5194/acp-11-321-2011, 2011.
Ion, A. C., Vermeylen, R., Kourtchev, I., Cafmeyer, J., Chi, X., Gelencsér, A., Maenhaut, W., and Claeys, M.: Polar organic compounds in rural PM2.5 aerosols from K-puszta, Hungary, during a 2003 summer field campaign: Sources and diel variations, Atmos. Chem. Phys., 5, 1805–1814, https://doi.org/10.5194/acp-5-1805-2005, 2005.
Janovics, R., Futó, I., and Molnár, M.: Sealed tube combustion
method with MnO2 for AMS 14C measurement, Radiocarbon, 60,
1347–1355, 2018.
Kanakidou, M., Seinfeld, J. H., Pandis, S. N., Barnes, I., Dentener, F. J., Facchini, M. C., Van Dingenen, R., Ervens, B., Nenes, A., Nielsen, C. J., Swietlicki, E., Putaud, J. P., Balkanski, Y., Fuzzi, S., Horth, J., Moortgat, G. K., Winterhalter, R., Myhre, C. E. L., Tsigaridis, K., Vignati, E., Stephanou, E. G., and Wilson, J.: Organic aerosol and global climate modelling: a review, Atmos. Chem. Phys., 5, 1053–1123, https://doi.org/10.5194/acp-5-1053-2005, 2005.
Kiss, G., Varga, B., Galambos, I., and Ganszky, I.: Characterization of
water-soluble organic matter isolated from atmospheric fine aerosol, J.
Geophys. Res., 107, 8339, https://doi.org/10.1029/2001JD000603, 2002.
Kourtchev, I., Hellebust, S., Bell, J. M., O'Connor, I. P., Healy, R. M.,
Allanic, A., Healy, D., Wenger, J. C., and Sodeau, J. R.: The use of polar
organic compounds to estimate the contribution of domestic solid fuel
combustion and biogenic sources to ambient levels of organic carbon and
PM2.5 in Cork Harbour, Ireland, Sci. Total Environ., 409, 2143–2155,
2011.
Kuhlbusch, Th. A. J., Borowiak, A., Gelencsér, A., Genberg, J., Gladtke,
D., Maenhaut, W., Pio, C., Popoviecheva, O., Putaud, J. P., Quincey, P.,
Sciare, J., ten Brink, H., Viana, M., and Yttri, K. E.: Measurement of
elemental and organic carbon in Europe, JRC Scientific and Technical
Reports, European Commission, Joint Research Centre, Ispra, 2009.
Lelieveld, J. and Pöschl, U.: Chemists can help to solve the
air-pollution health crisis, Nature, 551, 291–293, 2017.
Lohmann, U., Feichter, J., Penner, J., and Leaitch, R.: Indirect effect of
sulfate and carbonaceous aerosols: A mechanistic treatment, J. Geophys.
Res., 105, 12193–12206, 2000.
Maenhaut, W., Raes, N., Chi, X., Cafmeyer, J., Wang, W., and Salma, I.:
Chemical composition and mass closure for fine and coarse aerosols at a
kerbside in Budapest, Hungary, in spring 2002, X-ray Spectrom., 34,
290–296, 2005.
Maenhaut, W., Raes, N., Chi, X., Cafmeyer, J., and Wang, W.: Chemical
composition and mass closure for PM2.5 and PM10 aerosols at
K-puszta, Hungary, in summer 2006, X-ray Spectrom., 37, 193–197, 2008.
Maenhaut, W., Vermeylen, R., Claeys, M., Vercauteren, J., Matheeussen, C.,
and Roekens, E.: Assessment of the contribution from wood burning to the
PM10 aerosol in Flanders, Belgium, Sci. Total Environ., 437, 226–236,
2012.
Maenhaut, W., Vermeylen, R., Claeys, M., Vercauteren, J., and Roekens, E.:
Sources of the PM10 aerosol in Flanders, Belgium, and re-assessment of
the contribution from wood burning, Sci. Total Environ., 562, 550–560,
2016.
Major, I., Gyökös, B., Túri, M., Futó, I., Filep, Á.,
Hoffer, A., Furu, E., Jull, A. J. T., and Molnár, M.: Evaluation of an
automated EA-IRMS method for total carbon analysis of atmospheric aerosol at
HEKAL, J. Atmos. Chem., 75, 85–96, 2018.
McFiggans, G., Mentel, T. F., Wildt, J., Pullinen, I., Kang, S., Kleist, E.,
Schmitt, S., Springer, M., Tillmann, R., Wu, C., Zhao, D., Hallquist, M.,
Faxon, C., Le Breton, M., Hallquist, A. M., Simpson, D., Bergstroem, R.,
Jenkin, M. E., Ehn, M., Thornton, J. A., Alfarra, M. R., Bannan, T. J.,
Percival, C. J., Priestley, M., Topping, D., and Kiendler-Scharr, A.:
Secondary organic aerosol reduced by mixture of atmospheric vapours, Nature,
565, 587–593, 2019.
Minguillón, M. C., Perron, N., Querol, X., Szidat, S., Fahrni, S. M., Alastuey, A., Jimenez, J. L., Mohr, C., Ortega, A. M., Day, D. A., Lanz, V. A., Wacker, L., Reche, C., Cusack, M., Amato, F., Kiss, G., Hoffer, A., Decesari, S., Moretti, F., Hillamo, R., Teinilä, K., Seco, R., Peñuelas, J., Metzger, A., Schallhart, S., Müller, M., Hansel, A., Burkhart, J. F., Baltensperger, U., and Prévôt, A. S. H.: Fossil versus contemporary sources of fine elemental and organic carbonaceous particulate matter during the DAURE campaign in Northeast Spain, Atmos. Chem. Phys., 11, 12067–12084, https://doi.org/10.5194/acp-11-12067-2011, 2011.
Molnár, M., Rinyu, L., Veres, M., Seiler, M., Wacker, L., and Synal,
H.-A.: EnvironMICADAS: a mini 14C AMS with enhanced gas ion source
interface in the Hertelendi Laboratory of Environmental Studies, Hungary,
Radiocarbon, 55, 338–344, 2013.
Nolte, C. G., Schauer, J. J., Cass, G. R., and Simoneit, B. R. T.: Highly
polar organic compounds present in wood smoke and in the ambient atmosphere,
Environ. Sci. Technol., 35, 1912–1919, 2001.
Nozière, B., Kalberer, M., Claeys, M., Allan, J., D'Anna, B., Decesari,
S., Finessi, E., Glasius, M., Grgić, I., Hamilton, J. F., Hoffmann, T.,
Iinuma, Y., Jaoui, M., Kahnt, A., Kampf, C. J., Kourtchev, I., Maenhaut, W.,
Marsden, N., Saarikoski, S., Schnelle-Kreis, J., Surratt, J. D., Szidat, S.,
Szmigielski, R., and Wisthaler, A.: The molecular identification of organic
compounds in the atmosphere: state of the art and challenges, Chem. Rev.,
115, 3919–3983, 2015.
Panteliadis, P., Hafkenscheid, T., Cary, B., Diapouli, E., Fischer, A., Favez, O., Quincey, P., Viana, M., Hitzenberger, R., Vecchi, R., Saraga, D., Sciare, J., Jaffrezo, J. L., John, A., Schwarz, J., Giannoni, M., Novak, J., Karanasiou, A., Fermo, P., and Maenhaut, W.: ECOC comparison exercise with identical thermal protocols after temperature offset correction – instrument diagnostics by in-depth evaluation of operational parameters, Atmos. Meas. Tech., 8, 779–792, https://doi.org/10.5194/amt-8-779-2015, 2015.
Pashynska, V., Vermeylen, R., Vas, G., Maenhaut, W., and Claeys, M.:
Development of a gas chromatography/ion trap mass spectrometry method for
the determination of levoglucosan and saccharidic compounds in atmospheric
aerosols, Application to urban aerosols, J. Mass Spectrom., 37, 1249–125,
2002.
Piazzalunga, A., Belis, C., Bernardoni, V., Cazzuli, O., Fermo, P., Valli,
G., and Vecchi, R.: Estimates of wood burning contribution to PM by the
macro-tracer method using tailored emission factors, Atmos. Environ., 45,
6642–6649, 2011.
Putaud, J.-P., Van Dingenen, R., Alastuey, A., Bauer, H., Birmili, W.,
Cyrys, J., Flentje, H., Fuzzi, S., Gehrig, R., Hansson, H. C., Harrison, R.
M., Herrmann, H., Hitzenberger, R., Hüglin, C., Jones, A. M.,
Kasper-Giebl, A., Kiss, G., Kousa, A., Kuhlbusch, T. A. J., Löschau, G.,
Maenhaut, W., Molnár, A., Moreno, T., Pekkanen, J., Perrino, C., Pitz,
M., Puxbaum, H., Querol, X., Rodriguez, S., Salma, I., Schwarz, J., Smolik,
J., Schneider, J., Spindler, G., ten Brink, H., Tursic, J., Viana, M.,
Wiedensohler, A., and Raes, F.: A European aerosol phenomenology – 3:
physical and chemical characteristics of particulate matter from 60 rural,
urban, and kerbside sites across Europe, Atmos. Environ., 44, 1308–1320,
2010.
Puxbaum, H., Caseiro, A., Sanchez-Ochoa, A., Kasper-Giebl, A., Claeys, M.,
Gelencsér, A., Legrand, M., Preunkert, S., and Pio, C.: Levoglucosan
levels at background sites in Europe for assessing the impact of biomass
combustion on the European aerosol background, J. Geophys. Res.-Atmos., 112,
D23S05, https://doi.org/10.1029/2006JD008114, 2007.
Rap, A., Spracklen, D. V., Mercado, L., Reddington, C. L., Haywood, J. M.,
Ellis, R. J., Phillips, O. L., Artaxo, P., Bonal, D., Coupe, N. R., and
Butt, N.: Fires increase Amazon forest productivity through increases in
diffuse radiation, Geophys. Res. Lett., 42, 4654–4662, 2015.
Rosenfeld, D., Zhu, Y., Wang, M., Zheng, Y., Goren, T., and Yu, S.:
Aerosol-driven droplet concentrations dominate coverage and water of oceanic
low-level clouds, Science, 363, eaav0566, https://doi.org/10.1126/science.aav0566, 2019.
Russell, L. M.: Aerosol organic-mass-to-organic-carbon ratio measurements,
Environ. Sci. Technol., 37, 2982–2987, 2003.
Saarikoski, S., Timonen, H., Saarnio, K., Aurela, M., Järvi, L., Keronen, P., Kerminen, V.-M., and Hillamo, R.: Sources of organic carbon in fine particulate matter in northern European urban air, Atmos. Chem. Phys., 8, 6281–6295, https://doi.org/10.5194/acp-8-6281-2008, 2008.
Salma, I. and Maenhaut, W.: Changes in chemical composition and mass of
atmospheric aerosol pollution between 1996 and 2002 in a Central European
city, Environ. Pollut., 143, 479–488, 2006.
Salma, I., Maenhaut, W., Dubtsov, S., Zemplén-Papp, É., and
Záray, Gy.: Impact of phase out of leaded gasoline on the air quality in
Budapest, Microchem. J., 67, 127–133, 2000.
Salma, I., Chi, X., and Maenhaut, W.: Elemental and organic carbon in urban
canyon and background environments in Budapest, Hungary, Atmos. Environ.,
38, 27–36, 2004.
Salma, I., Ocskay, R., Chi, X., and Maenhaut, W.: Sampling artefacts,
concentrations and chemical composition of fine water-soluble organic carbon
and humic-like substances in a continental urban atmospheric environment,
Atmos. Environ., 41, 4106–4118, 2007.
Salma, I., Mészáros, T., and Maenhaut, W.: Mass size distribution of
carbon in atmospheric humic-like substances and water-soluble organic carbon
for an urban environment, J. Aerosol Sci., 56, 53–60, 2013.
Salma, I., Németh, Z., Weidinger, T., Kovács, B., and Kristóf, G.: Measurement, growth types and shrinkage of newly formed aerosol particles at an urban research platform, Atmos. Chem. Phys., 16, 7837–7851, https://doi.org/10.5194/acp-16-7837-2016, 2016a.
Salma, I., Németh, Z., Kerminen, V. M., Aalto, P., Nieminen, T.,
Weidinger, T., Molnár, Á., Imre, K., and Kulmala, M.: Regional
effect on urban atmospheric nucleation, Atmos. Chem. Phys., 16, 8715–8728,
2016b.
Salma, I., Németh, Z., Weidinger, T., Maenhaut, W., Claeys, M., Molnár, M., Major, I., Ajtai, T., Utry, N., and Bozóki, Z.: Source apportionment of carbonaceous chemical species to fossil fuel combustion, biomass burning and biogenic emissions by a coupled radiocarbon–levoglucosan marker method, Atmos. Chem. Phys., 17, 13767–13781, https://doi.org/10.5194/acp-17-13767-2017, 2017.
Sandradewi, J., Prévôt, A. S. H., Szidat, S., Perron, N., Alfarra,
R. M., Lanz, V. A., Weingartner, E., and Baltensperger, U.: Using aerosol
light absorption measurements for the quantitative determination of wood
burning and traffic emission contributions to particulate matter, Environ.
Sci. Technol., 42, 3316–3323, 2008a.
Sandradewi, J., Prévôt, A. S. H., Weingartner, E., Schmidhauser, R.,
Gysel, M., and Baltensperger, U.: A study of wood burning and traffic
aerosols in an Alpine valley using a multi-wavelength Aethalometer, Atmos.
Environ., 42, 101–112, 2008b.
Schmidl, C., Marr, L. L., Caseiro, A., Kotianova, P., Berner, A., Bauer, H.,
Kasper-Giebl, A., and Puxbaum, H.: Chemical characterisation of fine
particle emissions from wood stove combustion of common woods growing in
mid-European Alpine regions, Atmos. Environ., 42, 126–141, 2008.
Simoneit, B. R. T., Schauer, J. J., Nolte, C. G., Oros, D. R., Elias, V. O.,
Fraser, M. P., Rogge, W. F., and Cass, G. R.: Levoglucosan, a tracer for
cellulose in biomass burning and atmospheric particles, Atmos. Environ., 33,
173–182, 1999.
Simoneit, B. R. T., Elias, V. O., Kobayashi, M., Kawamura, K., Rushdi, A.
I., Medeiros, P. M., Rogge, W. F., and Didyk, B. M.: Sugars-dominant
water-soluble organic compounds in soils and characterization as tracers in
atmospheric particulate matter, Environ. Sci. Technol., 38, 5939–5949,
2004.
Stefenelli, G., Pospisilova, V., Lopez-Hilfiker, F. D., Daellenbach, K. R., Hüglin, C., Tong, Y., Baltensperger, U., Prévôt, A. S. H., and Slowik, J. G.: Organic aerosol source apportionment in Zurich using an extractive electrospray ionization time-of-flight mass spectrometer (EESI-TOF-MS) – Part 1: Biogenic influences and day–night chemistry in summer , Atmos. Chem. Phys., 19, 14825–14848, https://doi.org/10.5194/acp-19-14825-2019, 2019.
Swietlicki, E., Hansson, H. C., Hämeri, K., Svenningsson, B., Massling,
A., McFiggans, G., McMurry, P. H., Petäjä, T., Tunved, P., Gysel,
M., Topping, D., Weingartner, E., Baltensperger, U., Rissler, J.,
Wiedensohler, A., and Kulmala, M.: Hygroscopic properties of submicrometer
atmospheric aerosol particles measured with H-TDMA instruments in various
environments – a review, Tellus B, 60, 432–469, 2008.
Szidat, S., Jenk, T. M., Synal, H. A., Kalberer, M., Wacker, L., Hajdas, I.,
Kasper-Giebl, A., and Baltensperger, U.: Contributions of fossil fuel,
biomass-burning, and biogenic emissions to carbonaceous aerosols in Zurich
as traced by 14C, J. Geophys. Res., 111, D07206.
https://doi.org/10.1029/2005JD006590, 2006.
Szidat, S., Ruff, M., Perron, N., Wacker, L., Synal, H.-A., Hallquist, M., Shannigrahi, A. S., Yttri, K. E., Dye, C., and Simpson, D.: Fossil and non-fossil sources of organic carbon (OC) and elemental carbon (EC) in Göteborg, Sweden, Atmos. Chem. Phys., 9, 1521–1535, https://doi.org/10.5194/acp-9-1521-2009, 2009.
Tatai, Zs., Szőke, B., and Körmendi, K.: Budapest
zöldinfrastruktúra koncepciója (Concept on green infrastructure
of Budapest), Municipality of Budapest, BFVT Kft., Budapest, 2017 (in Hungarian).
Tian, H., Lu, C., Ciais, P., Michalak, A. M., Canadell, J. G., Saikawa, E.,
Huntzinger, D. N., Gurney, K. R., Sitch, S., Zhang, B., Yang, J., Bousquet,
P., Bruhwiler, L., Chen, G., Dlugokencky, E., Friedlingstein, P., Melillo,
J., Pan, S., Poulter, B., Prinn, R., Saunois, M., Schwalm, C. R., and Wofsy,
S. C.: The terrestrial biosphere as a net source of greenhouse gases to the
atmosphere, Nature, 531, 225–228, 2016.
Turpin, B. J. and Lim, H.-J.: Species contributions to PM2.5 mass
concentrations: revisiting common assumptions for estimating organic mass,
Aerosol Sci. Tech., 35, 602–610, 2001.
Turpin, B. J., Saxena, P., and Andrews, E.: Measuring and simulating
particulate organics in the atmosphere: problems and prospects, Atmos.
Environ., 34, 2983–3013, 2000.
Viana, M., Chi, X., Maenhaut, W., Cafmeyer, J., Querol, X., Alastuey, A.,
Mikuška, P., and Večeřa, Z.: Influence of sampling artefacts on
measured PM, OC, and EC levels in carbonaceous aerosols in an urban area,
Aerosol Sci. Tech., 40, 107–117, 2006.
Vicente, E. D. and Alves, C. A.: An overview of particulate emissions from
residential biomass combustion, Atmos. Res., 199, 159–185, 2018.
Von Schneidemesser, E., Monks, P. S., Allan, J. D., Bruhwiler, L., Forster,
P., Fowler, D., Lauer, A., Morgan, W. T., Paasonen, P., Righi, M.,
Sindelarova, K., and Sutton, M. A.: Chemistry and the linkages between air
quality and climate change, Chem. Rev., 115, 3856–3897, 2015.
Wacker, L., Bonani, G., Friedrich, M., Hajdas, I., Kromer, B., Némec,
M., Ruff, M., Suter, M., Synal, H.-A., and Vockenhuber, C.: MICADAS: Routine
and high-precision radiocarbon dating, Radiocarbon, 52, 252–262, 2010.
Wiedinmyer, C., Akagi, S. K., Yokelson, R. J., Emmons, L. K., Al-Saadi, J. A., Orlando, J. J., and Soja, A. J.: The Fire INventory from NCAR (FINN): a high resolution global model to estimate the emissions from open burning, Geosci. Model Dev., 4, 625–641, https://doi.org/10.5194/gmd-4-625-2011, 2011.
Yttri, K. E., Schnelle-Kreis, J., Maenhaut, W., Abbaszade, G., Alves, C., Bjerke, A., Bonnier, N., Bossi, R., Claeys, M., Dye, C., Evtyugina, M., García-Gacio, D., Hillamo, R., Hoffer, A., Hyder, M., Iinuma, Y., Jaffrezo, J.-L., Kasper-Giebl, A., Kiss, G., López-Mahia, P. L., Pio, C., Piot, C., Ramirez-Santa-Cruz, C., Sciare, J., Teinilä, K., Vermeylen, R., Vicente, A., and Zimmermann, R.: An intercomparison study of analytical methods used for quantification of levoglucosan in ambient aerosol filter samples, Atmos. Meas. Tech., 8, 125–147, https://doi.org/10.5194/amt-8-125-2015, 2015.
Zdráhal, Z., Oliveira, J., Vermeylen, R., Claeys, M., and Maenhaut, W.:
Improved method for quantifying levoglucosan and related monosaccharide
anhydrides in atmospheric aerosols and application to samples from urban and
tropical locations, Environ. Sci. Technol., 36, 747–753, 2002.
Zhang, Y. L., Perron, N., Ciobanu, V. G., Zotter, P., Minguillón, M. C., Wacker, L., Prévôt, A. S. H., Baltensperger, U., and Szidat, S.: On the isolation of OC and EC and the optimal strategy of radiocarbon-based source apportionment of carbonaceous aerosols, Atmos. Chem. Phys., 12, 10841–10856, https://doi.org/10.5194/acp-12-10841-2012, 2012.
Zotter, P., Herich, H., Gysel, M., El-Haddad, I., Zhang, Y., Močnik, G., Hüglin, C., Baltensperger, U., Szidat, S., and Prévôt, A. S. H.: Evaluation of the absorption Ångström exponents for traffic and wood burning in the Aethalometer-based source apportionment using radiocarbon measurements of ambient aerosol, Atmos. Chem. Phys., 17, 4229–4249, https://doi.org/10.5194/acp-17-4229-2017, 2017.
Short summary
Major carbonaceous aerosol species were apportioned among FF combustion, BB and biogenic sources in various types of atmospheric environments of interest in the Carpathian Basin in different months representing different seasons. The conclusions present novel and valuable research contributions on a large area in central Europe.
Major carbonaceous aerosol species were apportioned among FF combustion, BB and biogenic sources...
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