Articles | Volume 16, issue 4
https://doi.org/10.5194/acp-16-1971-2016
© 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-16-1971-2016
© Author(s) 2016. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Research article
| 
23 Feb 2016
Research article |
| 23 Feb 2016
Speciation of 127I and 129I in atmospheric aerosols at Risø, Denmark: insight into sources of iodine isotopes and their species transformations
Luyuan Zhang
Center for Nuclear Technologies, Technical University of
Denmark, Risø Campus, Roskilde 4000, Denmark
State Key Laboratory of Loess and Quaternary Geology, Shaanxi Key Laboratory of AMS Technology and
Application, Xi'an AMS Center, Institute of Earth
Environment, Chinese Academy of Sciences, Xi'an 710061, China
Center for Nuclear Technologies, Technical University of
Denmark, Risø Campus, Roskilde 4000, Denmark
State Key Laboratory of Loess and Quaternary Geology, Shaanxi Key Laboratory of AMS Technology and
Application, Xi'an AMS Center, Institute of Earth
Environment, Chinese Academy of Sciences, Xi'an 710061, China
Sheng Xu
Scottish Universities Environmental Research Center, East
Kilbride, G75 0QF, UK
Related authors
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Luyuan Zhang, Xiaolin Hou, Sheng Xu, Tian Feng, Peng Cheng, Yunchong Fu, and Ning Chen
Atmos. Chem. Phys., 20, 2623–2635, https://doi.org/10.5194/acp-20-2623-2020, https://doi.org/10.5194/acp-20-2623-2020, 2020
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To trace the long-range transport of air pollutants and understand the atmospheric effect of iodine, the daily-resolution temporal variations of 129I and 127I in aerosols from a monsoonal city indicate the East Asian monsoon and fossil fuel combustion plays crucial roles on transport of 129I from Europe to East Asia and on elevated 127I concentrations. Through linking iodine isotopes with five major air pollutants, this study proposes the possible role of iodine in urban air pollution.
P. P. Povinec, M. Aoyama, D. Biddulph, R. Breier, K. Buesseler, C. C. Chang, R. Golser, X. L. Hou, M. Ješkovský, A. J. T. Jull, J. Kaizer, M. Nakano, H. Nies, L. Palcsu, L. Papp, M. K. Pham, P. Steier, and L. Y. Zhang
Biogeosciences, 10, 5481–5496, https://doi.org/10.5194/bg-10-5481-2013, https://doi.org/10.5194/bg-10-5481-2013, 2013
Related subject area
Subject: Aerosols | Research Activity: Field Measurements | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Molecular characterization of organic aerosols in urban and forested areas of Paris using high-resolution mass spectrometry
Measurement report: Wintertime aerosol characterization at an urban traffic site in Helsinki, Finland
Source apportionment and ecotoxicity of PM2.5 pollution events in a major Southern Hemisphere megacity: influence of a biofuel-impacted fleet and biomass burning
Marine organic aerosol at Mace Head: effects from phytoplankton and source region variability
Measurement report: Sources and meteorology influencing highly time-resolved PM2.5 trace elements at three urban sites in the extremely polluted Indo-Gangetic Plain in India
Formation of highly absorptive secondary brown carbon through nighttime multiphase chemistry of biomass burning emissions
Measurement report: Vertically resolved atmospheric properties observed over the Southern Great Plains with the ArcticShark uncrewed aerial system
Non-biogenic sources are an important but overlooked contributor to aerosol isoprene-derived organosulfates during winter in northern China
The critical role of aqueous-phase processes in aromatic-derived nitrogen-containing organic aerosol formation in cities with different energy consumption patterns
Characterization of atmospheric water-soluble brown carbon in the Athabasca oil sands region, Canada
Sensitivity of aerosol and cloud properties to coupling strength of marine boundary layer clouds over the northwest Atlantic
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
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
High-resolution analyses of concentrations and sizes of refractory black carbon particles deposited in northwestern Greenland over the past 350 years – Part 2: Seasonal and temporal trends in refractory black carbon originated from fossil fuel combustion and biomass burning
Direct measurement of N2O5 heterogeneous uptake coefficients on atmospheric aerosols in southwestern China and evaluation of current parameterizations
Measurement report: Per- and polyfluoroalkyl substances (PFAS) in particulate matter (PM10) from activated sludge aeration
Significant role of biomass burning in heavy haze formation in Nanjing, a megacity in China: molecular-level insights from intensive PM2.5 sampling on winter hazy days
Widespread trace bromine and iodine in remote tropospheric non-sea-salt aerosols
Significant contributions of biomass burning to PM2.5-bound aromatic compounds: insights from field observations and quantum chemical calculations
A 60-year atmospheric nitrate isotope record from a Southeast Greenland ice core with minimal post-depositional alteration
Iron isotopes reveal significant aerosol dissolution over the Pacific Ocean
Formation and chemical evolution of secondary organic aerosol in two different environments: a dual-chamber study
Enrichment of organic nitrogen in fog residuals observed in the Italian Po Valley
Technical note: Quantified organic aerosol subsaturated hygroscopicity by a simple optical scatter monitor system through field measurements
Measurement report: Oxidation potential of water-soluble aerosol components in the south and north of Beijing
Enhanced daytime secondary aerosol formation driven by gas–particle partitioning in downwind urban plumes
Technical note: Reconstructing surface missing aerosol elemental carbon data in long-term series with ensemble learning
Understanding the mechanism and importance of brown carbon bleaching across the visible spectrum in biomass burning plumes from the WE-CAN campaign
Influence of terrestrial and marine air mass on the constituents and intermixing of bioaerosols over a coastal atmosphere
A multi-site passive approach to studying the emissions and evolution of smoke from prescribed fires
The annual cycle and sources of relevant aerosol precursor vapors in the central Arctic during the MOSAiC expedition
Enhanced emission of intermediate/semi-volatile organic matters in both gas and particle phases from ship exhausts with low-sulfur fuels
Advances in characterization of black carbon particles and their associated coatings using the soot particle aerosol mass spectrometer in Singapore, a complex city environment
Measurement report: Crustal materials play an increasing role in elevating particle pH: Insights from 12-year records in a typical inland city of China
African dust transported to Barbados in the Wintertime Lacks Indicators of Chemical Aging
Opinion: How will advances in aerosol science inform our understanding of the health impacts of outdoor particulate pollution?
Machine Learning Assisted Chemical Characterization and Optical Properties of Atmospheric Brown Carbon in Nanjing, China
Measurement report: Intra-annual variability of black carbon and brown carbon and their interrelation with meteorological conditions over Gangtok, Sikkim
Long-range transport of air pollutants increases the concentration of hazardous components of PM2.5 in northern South America
Dominant influence of biomass combustion and cross-border transport on nitrogen-containing organic compound levels in the southeastern Tibetan Plateau
Impacts of elevated anthropogenic emissions on physicochemical characteristics of black-carbon-containing particles over the Tibetan Plateau
Online characterization of primary and secondary emissions of particulate matter and acidic molecules from a modern fleet of city buses
Atmospheric evolution of environmentally persistent free radicals in the rural North China Plain: effects on water solubility and PM2.5 oxidative potential
Measurement report: Characterization of Aerosol Hygroscopicity over Southeast Asia during the NASA CAMP2Ex Campaign
Two distinct ship emission profiles for organic-sulfate source apportionment of PM in sulfur emission control areas
Measurement report: In-depth characterization of ship emissions during operations in a Mediterranean port
Diana L. Pereira, Chiara Giorio, Aline Gratien, Alexander Zherebker, Gael Noyalet, Servanne Chevaillier, Stéphanie Alage, Elie Almarj, Antonin Bergé, Thomas Bertin, Mathieu Cazaunau, Patrice Coll, Ludovico Di Antonio, Sergio Harb, Johannes Heuser, Cécile Gaimoz, Oscar Guillemant, Brigitte Language, Olivier Lauret, Camilo Macias, Franck Maisonneuve, Bénédicte Picquet-Varrault, Raquel Torres, Sylvain Triquet, Pascal Zapf, Lelia Hawkins, Drew Pronovost, Sydney Riley, Pierre-Marie Flaud, Emilie Perraudin, Pauline Pouyes, Eric Villenave, Alexandre Albinet, Olivier Favez, Robin Aujay-Plouzeau, Vincent Michoud, Christopher Cantrell, Manuela Cirtog, Claudia Di Biagio, Jean-François Doussin, and Paola Formenti
Atmos. Chem. Phys., 25, 4885–4905, https://doi.org/10.5194/acp-25-4885-2025, https://doi.org/10.5194/acp-25-4885-2025, 2025
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In order to study aerosols in environments influenced by anthropogenic and biogenic emissions, we performed analyses of samples collected during the ACROSS (Atmospheric Chemistry Of the Suburban Forest) campaign in summer 2022 in the greater Paris area. After analysis of the chemical composition by means of total carbon determination and high-resolution mass spectrometry, this work highlights the influence of anthropogenic inputs on the chemical composition of both urban and forested areas.
Kimmo Teinilä, Sanna Saarikoski, Henna Lintusaari, Teemu Lepistö, Petteri Marjanen, Minna Aurela, Heidi Hellén, Toni Tykkä, Markus Lampimäki, Janne Lampilahti, Luis Barreira, Timo Mäkelä, Leena Kangas, Juha Hatakka, Sami Harni, Joel Kuula, Jarkko V. Niemi, Harri Portin, Jaakko Yli-Ojanperä, Ville Niemelä, Milja Jäppi, Katrianne Lehtipalo, Joonas Vanhanen, Liisa Pirjola, Hanna E. Manninen, Tuukka Petäjä, Topi Rönkkö, and Hilkka Timonen
Atmos. Chem. Phys., 25, 4907–4928, https://doi.org/10.5194/acp-25-4907-2025, https://doi.org/10.5194/acp-25-4907-2025, 2025
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Physical and chemical properties of particulate matter and concentrations of trace gases were measured in a street canyon in Helsinki, Finland, and an urban background site in January–February 2022 to investigate the effect of wintertime conditions on pollutants. State-of-the-art instruments and a mobile laboratory were used, and the measurement data were analysed further with modelling tools like positive matrix factorization and the Pollution Detection Algorithm.
Guilherme Martins Pereira, Leonardo Yoshiaki Kamigauti, Rubens Fabio Pereira, Djacinto Monteiro dos Santos, Thayná da Silva Santos, José Vinicius Martins, Célia Alves, Cátia Gonçalves, Ismael Casotti Rienda, Nora Kováts, Thiago Nogueira, Luciana Rizzo, Paulo Artaxo, Regina Maura de Miranda, Marcia Akemi Yamasoe, Edmilson Dias de Freitas, Pérola de Castro Vasconcellos, and Maria de Fatima Andrade
Atmos. Chem. Phys., 25, 4587–4616, https://doi.org/10.5194/acp-25-4587-2025, https://doi.org/10.5194/acp-25-4587-2025, 2025
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The chemical composition of fine particulate matter was studied in the megacity of São Paulo (Brazil) during a polluted period. Vehicular-related sources remain relevant; however, a high contribution of biomass burning was observed and correlated with sample ecotoxicity. Emerging biomass burning sources, such as forest fires and sugarcane-bagasse-based power plants, highlight the need for additional control measures alongside stricter rules concerning vehicular emissions.
Emmanuel Chevassus, Kirsten N. Fossum, Darius Ceburnis, Lu Lei, Chunshui Lin, Wei Xu, Colin O'Dowd, and Jurgita Ovadnevaite
Atmos. Chem. Phys., 25, 4107–4129, https://doi.org/10.5194/acp-25-4107-2025, https://doi.org/10.5194/acp-25-4107-2025, 2025
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This study presents the first source apportionment of organic aerosol at Mace Head via high-resolution mass spectrometry. Introducing transfer entropy as a novel method reveals that aged organic aerosol originates from both open-ocean ozonolysis and local peat-burning oxidation. Methanesulfonic acid and organic sea spray both mirror phytoplankton activity, with the former closely tied to coccolithophore blooms and the latter linked to diatoms, chlorophytes, and cyanobacteria.
Ashutosh K. Shukla, Sachchida N. Tripathi, Shamitaksha Talukdar, Vishnu Murari, Sreenivas Gaddamidi, Manousos-Ioannis Manousakas, Vipul Lalchandani, Kuldeep Dixit, Vinayak M. Ruge, Peeyush Khare, Mayank Kumar, Vikram Singh, Neeraj Rastogi, Suresh Tiwari, Atul K. Srivastava, Dilip Ganguly, Kaspar Rudolf Daellenbach, and André S. H. Prévôt
Atmos. Chem. Phys., 25, 3765–3784, https://doi.org/10.5194/acp-25-3765-2025, https://doi.org/10.5194/acp-25-3765-2025, 2025
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Our study delves into the elemental composition of aerosols at three sites across the Indo-Gangetic Plain (IGP), revealing distinct patterns during pollution episodes. We found significant increases in chlorine (Cl)-rich and solid fuel combustion (SFC) sources, indicating dynamic emission sources, agricultural burning impacts, and meteorological influences. Surges in Cl-rich particles during cold periods highlight their role in particle growth under high-relative-humidity conditions.
Ye Kuang, Biao Luo, Shan Huang, Junwen Liu, Weiwei Hu, Yuwen Peng, Duohong Chen, Dingli Yue, Wanyun Xu, Bin Yuan, and Min Shao
Atmos. Chem. Phys., 25, 3737–3752, https://doi.org/10.5194/acp-25-3737-2025, https://doi.org/10.5194/acp-25-3737-2025, 2025
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This research reveals the potential importance of nighttime NO3 radical chemistry and aerosol water in the rapid formation of secondary brown carbon from diluted biomass burning emissions. The findings enhance our understanding of nighttime biomass burning evolution and its implications for climate and regional air quality, especially regarding interactions with background aerosol water and water-rich fogs and clouds.
Fan Mei, Qi Zhang, Damao Zhang, Jerome D. Fast, Gourihar Kulkarni, Mikhail S. Pekour, Christopher R. Niedek, Susanne Glienke, Israel Silber, Beat Schmid, Jason M. Tomlinson, Hardeep S. Mehta, Xena Mansoura, Zezhen Cheng, Gregory W. Vandergrift, Nurun Nahar Lata, Swarup China, and Zihua Zhu
Atmos. Chem. Phys., 25, 3425–3444, https://doi.org/10.5194/acp-25-3425-2025, https://doi.org/10.5194/acp-25-3425-2025, 2025
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This study highlights the unique capability of the ArcticShark, an uncrewed aerial system, in measuring vertically resolved atmospheric properties. Data from 32 research flights in 2023 reveal seasonal patterns and correlations with conventional measurements. The consistency and complementarity of in situ and remote sensing methods are highlighted. The study demonstrates the ArcticShark’s versatility in bridging data gaps and improving the understanding of vertical atmospheric structures.
Ting Yang, Yu Xu, Yu-Chen Wang, Yi-Jia Ma, Hong-Wei Xiao, Hao Xiao, and Hua-Yun Xiao
Atmos. Chem. Phys., 25, 2967–2978, https://doi.org/10.5194/acp-25-2967-2025, https://doi.org/10.5194/acp-25-2967-2025, 2025
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Previous measurement–model comparisons of atmospheric isoprene levels showed a significant unidentified source of isoprene in some northern Chinese cities during winter. Here, the first combination of large-scale observations and field combustion experiments provides novel insights into biomass burning emissions as a significant source of isoprene-derived organosulfates during winter in northern cities of China.
Yi-Jia Ma, Yu Xu, Ting Yang, Lin Gui, Hong-Wei Xiao, Hao Xiao, and Hua-Yun Xiao
Atmos. Chem. Phys., 25, 2763–2780, https://doi.org/10.5194/acp-25-2763-2025, https://doi.org/10.5194/acp-25-2763-2025, 2025
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The abundance, potential precursors, and main formation mechanisms of nitrogen-containing organic compounds (NOCs) in PM2.5 during winter were compared among cities with different energy consumption patterns. The aerosol NOC pollution during winter in China is closely associated with the intensity of precursor emissions and the aqueous-phase processes. Our results highlight the importance of emission reduction strategies in controlling aerosol NOCs pollution during winter in China.
Dane Blanchard, Mark Gordon, Duc Huy Dang, Paul Andrew Makar, and Julian Aherne
Atmos. Chem. Phys., 25, 2423–2442, https://doi.org/10.5194/acp-25-2423-2025, https://doi.org/10.5194/acp-25-2423-2025, 2025
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This study offers the first known evaluation of water-soluble brown carbon aerosols in the Athabasca oil sands region (AOSR), Canada. Fluorescence spectroscopy analysis of aerosol samples from five regional sites (collected during the summer of 2021) identified oil sands operations as a measurable brown carbon source. Industrial aerosol emissions were unlikely to impact regional radiative forcing. These findings show that fluorescence spectroscopy can be used to monitor brown carbon in the AOSR.
Kira Zeider, Kayla McCauley, Sanja Dmitrovic, Leong Wai Siu, Yonghoon Choi, Ewan C. Crosbie, Joshua P. DiGangi, Glenn S. Diskin, Simon Kirschler, John B. Nowak, Michael A. Shook, Kenneth L. Thornhill, Christiane Voigt, Edward L. Winstead, Luke D. Ziemba, Paquita Zuidema, and Armin Sorooshian
Atmos. Chem. Phys., 25, 2407–2422, https://doi.org/10.5194/acp-25-2407-2025, https://doi.org/10.5194/acp-25-2407-2025, 2025
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In situ aircraft data collected over the northwest Atlantic Ocean are utilized to compare aerosol conditions and turbulence between near-surface and below-cloud-base altitudes for different regimes of coupling strength between those two levels, along with how cloud microphysical properties vary across those regimes. Stronger coupling yields more homogenous aerosol structure vertically along with higher cloud drop concentrations and sea salt influence in clouds.
Amie Dobracki, Ernie R. Lewis, Arthur J. Sedlacek III, Tyler Tatro, Maria A. Zawadowicz, and Paquita Zuidema
Atmos. Chem. Phys., 25, 2333–2363, https://doi.org/10.5194/acp-25-2333-2025, https://doi.org/10.5194/acp-25-2333-2025, 2025
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Biomass-burning aerosol is commonly present in the marine boundary layer over the southeast Atlantic Ocean between June and October. Our research indicates that burning conditions, aerosol transport pathways, and prolonged oxidation processes (heterogeneous and aqueous phases) determine the chemical, microphysical, and optical properties of the boundary layer aerosol. Notably, we find that the aerosol optical properties can be estimated from the chemical properties alone.
Benjamin Heutte, Nora Bergner, Hélène Angot, Jakob B. Pernov, Lubna Dada, Jessica A. Mirrielees, Ivo Beck, Andrea Baccarini, Matthew Boyer, Jessie M. Creamean, Kaspar R. Daellenbach, Imad El Haddad, Markus M. Frey, Silvia Henning, Tiia Laurila, Vaios Moschos, Tuukka Petäjä, Kerri A. Pratt, Lauriane L. J. Quéléver, Matthew D. Shupe, Paul Zieger, Tuija Jokinen, and Julia Schmale
Atmos. Chem. Phys., 25, 2207–2241, https://doi.org/10.5194/acp-25-2207-2025, https://doi.org/10.5194/acp-25-2207-2025, 2025
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Limited aerosol measurements in the central Arctic hinder our understanding of aerosol–climate interactions in the region. Our year-long observations of aerosol physicochemical properties during the MOSAiC expedition reveal strong seasonal variations in aerosol chemical composition, where the short-term variability is heavily affected by storms in the Arctic. Local wind-generated particles are shown to be an important source of cloud seeds, especially in autumn.
Feng Jiang, Harald Saathoff, Uzoamaka Ezenobi, Junwei Song, Hengheng Zhang, Linyu Gao, and Thomas Leisner
Atmos. Chem. Phys., 25, 1917–1930, https://doi.org/10.5194/acp-25-1917-2025, https://doi.org/10.5194/acp-25-1917-2025, 2025
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The chemical composition of brown carbon in the particle and gas phase was determined by mass spectrometry. BrC in the gas phase was mainly controlled by secondary formation and particle-to-gas partitioning. BrC in the particle phase was mainly from secondary formation. This work helps to get a better understanding of diurnal variations and the sources of brown carbon aerosol at a rural location in central Europe.
James Brean, David C. S. Beddows, Eija Asmi, Aki Virkkula, Lauriane L. J. Quéléver, Mikko Sipilä, Floortje Van Den Heuvel, Thomas Lachlan-Cope, Anna Jones, Markus Frey, Angelo Lupi, Jiyeon Park, Young Jun Yoon, Rolf Weller, Giselle L. Marincovich, Gabriela C. Mulena, Roy M. Harrison, and Manuel Dall'Osto
Atmos. Chem. Phys., 25, 1145–1162, https://doi.org/10.5194/acp-25-1145-2025, https://doi.org/10.5194/acp-25-1145-2025, 2025
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Our results emphasise how understanding the geographical variation in surface types across the Antarctic is key to understanding secondary aerosol sources.
Adam E. Thomas, Hayley S. Glicker, Alex B. Guenther, Roger Seco, Oscar Vega Bustillos, Julio Tota, Rodrigo A. F. Souza, and James N. Smith
Atmos. Chem. Phys., 25, 959–977, https://doi.org/10.5194/acp-25-959-2025, https://doi.org/10.5194/acp-25-959-2025, 2025
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We present measurements of the organic composition of ultrafine particles collected from the eastern Amazon, an understudied region that is subjected to increasing human influence. We find that while isoprene chemistry is likely significant for ultrafine-particle growth throughout the year, compounds related to other sources, such as biological-spore emissions and biomass burning, exhibit striking seasonal differences, implying extensive variation in regional ultrafine-particle sources.
Xiufeng Lian, Yongjiang Xu, Fengxian Liu, Long Peng, Xiaodong Hu, Guigang Tang, Xu Dao, Hui Guo, Liwei Wang, Bo Huang, Chunlei Cheng, Lei Li, Guohua Zhang, Xinhui Bi, Xiaofei Wang, Zhen Zhou, and Mei Li
EGUsphere, https://doi.org/10.5194/egusphere-2024-3469, https://doi.org/10.5194/egusphere-2024-3469, 2025
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In this study, we analyzed the mixing state and atmospheric chemical processes of Pb-rich single particles in Beijing. Then, we focused on analyzing the differences in Pb-rich particles between the heating period and non-heating period, as well as the formation mechanism of lead nitrate after coal-to-gas conversion. Our results highlighted the improvement of coal-to-gas conversion on Pb in the particulate.
Kumiko Goto-Azuma, Yoshimi Ogawa-Tsukagawa, Kaori Fukuda, Koji Fujita, Motohiro Hirabayashi, Remi Dallmayr, Jun Ogata, Nobuhiro Moteki, Tatsuhiro Mori, Sho Ohata, Yutaka Kondo, Makoto Koike, Sumito Matoba, Moe Kadota, Akane Tsushima, Naoko Nagatsuka, and Teruo Aoki
Atmos. Chem. Phys., 25, 657–683, https://doi.org/10.5194/acp-25-657-2025, https://doi.org/10.5194/acp-25-657-2025, 2025
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Monthly ice core records spanning 350 years from Greenland show trends in refractory black carbon (rBC) concentrations and sizes. rBC levels have increased since the 1870s due to the inflow of anthropogenic rBC, with larger diameters than those from biomass burning (BB) rBC. High summer BB rBC peaks may reduce the ice sheet albedo, but BB rBC showed no increase until the early 2000s. These results are vital for validating aerosol and climate models.
Jiayin Li, Tianyu Zhai, Xiaorui Chen, Haichao Wang, Shuyang Xie, Shiyi Chen, Chunmeng Li, Huabin Dong, and Keding Lu
EGUsphere, https://doi.org/10.5194/egusphere-2024-3804, https://doi.org/10.5194/egusphere-2024-3804, 2025
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We directly measured the dinitrogen pentoxide (N2O5) uptake coefficient which critical impact the NOx fate and particulate nitrate formation in a typical highland city, Kunming, in China. We found the performance of current γ(N2O5) parameterizations showed deviations with the varying aerosol liquid water content (ALWC). Such differences would lead to biased estimation on particulate nitrate production potential. Our findings suggest the directions for future studies.
Jishnu Pandamkulangara Kizhakkethil, Zongbo Shi, Anna Bogush, and Ivan Kourtchev
EGUsphere, https://doi.org/10.5194/egusphere-2024-3952, https://doi.org/10.5194/egusphere-2024-3952, 2025
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Pollution with per- and polyfluoroalkyl substances (PFAS) received attention due to their environmental persistence and bioaccumulation. PM10 collected above a scaled-down activated sludge tank treating domestic sewage for a population >10,000 people in the UK were 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.
Mingjie Kang, Mengying Bao, Wenhuai Song, Aduburexiati Abulimiti, Changliu Wu, Fang Cao, Sönke Szidat, and Yanlin Zhang
Atmos. Chem. Phys., 25, 73–91, https://doi.org/10.5194/acp-25-73-2025, https://doi.org/10.5194/acp-25-73-2025, 2025
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Reports on molecular-level knowledge of high-temporal-resolution particulate matter ≤2.5 µm in diameter (PM2.5) on hazy days are limited. We investigated various PM2.5 species and their sources. The results show biomass burning (BB) was the main source of organic carbon. Moreover, BB enhanced fungal spore emissions and secondary aerosol formation. The contribution of non-fossil sources increased with increasing haze pollution, suggesting BB may be an important driver of haze events in winter.
Gregory P. Schill, Karl D. Froyd, Daniel M. Murphy, Christina J. Williamson, Charles A. Brock, Tomás Sherwen, Mat J. Evans, Eric A. Ray, Eric C. Apel, Rebecca S. Hornbrook, Alan J. Hills, Jeff Peischl, Thomas B. Ryerson, Chelsea R. Thompson, Ilann Bourgeois, Donald R. Blake, Joshua P. DiGangi, and Glenn S. Diskin
Atmos. Chem. Phys., 25, 45–71, https://doi.org/10.5194/acp-25-45-2025, https://doi.org/10.5194/acp-25-45-2025, 2025
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Using single-particle mass spectrometry, we show that trace concentrations of bromine and iodine are ubiquitous in remote tropospheric aerosol and suggest that aerosols are an important part of the global reactive iodine budget. Comparisons to a global climate model with detailed iodine chemistry are favorable in the background atmosphere; however, the model cannot replicate our measurements near the ocean surface, in biomass burning plumes, and in the stratosphere.
Yanqin Ren, Zhenhai Wu, Fang Bi, Hong Li, Haijie Zhang, Junling Li, Rui Gao, Fangyun Long, Zhengyang Liu, Yuanyuan Ji, and Gehui Wang
EGUsphere, https://doi.org/10.5194/egusphere-2024-3678, https://doi.org/10.5194/egusphere-2024-3678, 2025
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The daily concentrations of Polycyclic aromatic hydrocarbons (PAHs), oxygenated PAHs (OPAHs), and nitrated phenols (NPs) in PM2.5 were all increased during the heating season. Biomass burning was identified to be the primary source of these aromatic compounds, particularly for PAHs. Phenol and nitrobenzene are two main primary precursors for 4NP, with phenol showing lower reaction barriers. P-Cresol was identified as the primary precursor for the formation of 4-methyl-5-nitrocatechol.
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
EGUsphere, https://doi.org/10.5194/egusphere-2024-3937, https://doi.org/10.5194/egusphere-2024-3937, 2024
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Nitrate isotope records in ice cores reveal changes in NOₓ emissions, atmospheric acidity, and oxidation chemistry driven by human activity. However, nitrate in snow can be altered by UV-driven post-depositional processes, making snow accumulation rates critical for preserving these records. This study examines nitrate isotopes in an SE-Dome ice core, where high snow accumulation minimizes these effects, providing a reliable archive of atmospheric nitrogen cycling.
Capucine Camin, François Lacan, Catherine Pradoux, Marie Labatut, Anne Johansen, and James W. Murray
EGUsphere, https://doi.org/10.5194/egusphere-2024-3777, https://doi.org/10.5194/egusphere-2024-3777, 2024
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This manuscript presents the chemical composition of aerosols (> 1µm) over the Equatorial and Tropical Pacific Ocean, presenting the first measurements of iron isotopes in aerosols from this region. Iron concentrations and isotopes were determined using a Neptune MC-ICPMS. Our data analysis reveals that a significant portion of the aerosols undergo dissolution and removal during atmospheric transport. These findings contribute to original conclusions about the chemistry and physics of aerosols.
Andreas Aktypis, Dontavious J. Sippial, Christina N. Vasilakopoulou, Angeliki Matrali, Christos Kaltsonoudis, Andrea Simonati, Marco Paglione, Matteo Rinaldi, Stefano Decesari, and Spyros N. Pandis
Atmos. Chem. Phys., 24, 13769–13791, https://doi.org/10.5194/acp-24-13769-2024, https://doi.org/10.5194/acp-24-13769-2024, 2024
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A dual-chamber system was deployed in two different environments (Po Valley, Italy, and Pertouli forest, Greece) to study the potential of ambient air directly injected into the chambers, to form secondary organic aerosol (SOA). In the Po Valley, the system reacts rapidly, forming large amounts of SOA, while in Pertouli the SOA formation chemistry appears to have been practically terminated before the beginning of most experiments, so there is little additional SOA formation potential left.
Fredrik Mattsson, Almuth Neuberger, Liine Heikkinen, Yvette Gramlich, Marco Paglione, Matteo Rinaldi, Stefano Decesari, Paul Zieger, Ilona Riipinen, and Claudia Mohr
EGUsphere, https://doi.org/10.5194/egusphere-2024-3629, https://doi.org/10.5194/egusphere-2024-3629, 2024
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This study investigated aerosol-cloud interactions, focusing on organic nitrogen (ON) formation in the aqueous phase. Measurements were conducted in wintertime Italian Po Valley, using aerosol mass spectrometry. The fog was enriched in more hygroscopic inorganic compounds and ON, containing e.g. imidazoles. The formation of imidazole by aerosol-fog interactions could be confirmed for the first time in atmospheric observations. Findings highlight the role of fog in nitrogen aerosol formation.
Jie Zhang, Tianyu Zhu, Alexandra Catena, Yaowei Li, Margaret J. Schwab, Pengfei Liu, Akua Asa-Awuku, and James Schwab
Atmos. Chem. Phys., 24, 13445–13456, https://doi.org/10.5194/acp-24-13445-2024, https://doi.org/10.5194/acp-24-13445-2024, 2024
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This study shows the derived organic aerosol hygroscopicity under high-humidity conditions based on a simple optical scatter monitor system, including two nephelometric monitors (pDR-1500), when the aerosol chemical composition is already known.
Wei Yuan, Ru-Jin Huang, Chao Luo, Lu Yang, Wenjuan Cao, Jie Guo, and Huinan Yang
Atmos. Chem. Phys., 24, 13219–13230, https://doi.org/10.5194/acp-24-13219-2024, https://doi.org/10.5194/acp-24-13219-2024, 2024
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We characterized water-soluble oxidative potential (OP) levels in wintertime PM2.5 in the south and north of Beijing. Our results show that the volume-normalized dithiothreitol (DTTv) in the north was comparable to that in the south, while the mass-normalized dithiothreitol (DTTm) in the north was almost twice that in the south. Traffic-related emissions and biomass burning were the main sources of DTTv in the south, and traffic-related emissions contributed the most to DTTv in the north.
Mingfu Cai, Chenshuo Ye, Bin Yuan, Shan Huang, E Zheng, Suxia Yang, Zelong Wang, Yi Lin, Tiange Li, Weiwei Hu, Wei Chen, Qicong Song, Wei Li, Yuwen Peng, Baoling Liang, Qibin Sun, Jun Zhao, Duohong Chen, Jiaren Sun, Zhiyong Yang, and Min Shao
Atmos. Chem. Phys., 24, 13065–13079, https://doi.org/10.5194/acp-24-13065-2024, https://doi.org/10.5194/acp-24-13065-2024, 2024
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This study investigated the daytime secondary organic aerosol (SOA) formation in urban plumes. We observed a significant daytime SOA formation through gas–particle partitioning when the site was affected by urban plumes. A box model simulation indicated that urban pollutants (nitrogen oxide and volatile organic compounds) could enhance the oxidizing capacity, while the elevated volatile organic compounds were mainly responsible for promoting daytime SOA formation.
Qingxiao Meng, Yunjiang Zhang, Sheng Zhong, Jie Fang, Lili Tang, Yongcai Rao, Minfeng Zhou, Jian Qiu, Xiaofeng Xu, Jean-Eudes Petit, Olivier Favez, and Xinlei Ge
EGUsphere, https://doi.org/10.5194/egusphere-2024-2776, https://doi.org/10.5194/egusphere-2024-2776, 2024
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We developed a new method to reconstruct missing elemental carbon (EC) data in four Chinese cities from 2013 to 2023. Using machine learning, we accurately filled data gaps and introduced a new approach to analyze EC trends. Our findings reveal a significant decline in EC due to stricter pollution controls, though this slowed after 2020. This study provides a versatile framework for addressing data gaps and supports strategies to reduce urban air pollution and its climate impacts.
Yingjie Shen, Rudra P. Pokhrel, Amy P. Sullivan, Ezra J. T. Levin, Lauren A. Garofalo, Delphine K. Farmer, Wade Permar, Lu Hu, Darin W. Toohey, Teresa Campos, Emily V. Fischer, and Shane M. Murphy
Atmos. Chem. Phys., 24, 12881–12901, https://doi.org/10.5194/acp-24-12881-2024, https://doi.org/10.5194/acp-24-12881-2024, 2024
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The magnitude and evolution of brown carbon (BrC) absorption remain unclear, with uncertainty in climate models. Data from the WE-CAN airborne experiment show that model parameterizations overestimate the mass absorption cross section (MAC) of BrC. Observed decreases in BrC absorption with chemical markers are due to decreasing organic aerosol (OA) mass rather than a decreasing BrC MAC, which is currently implemented in models. Water-soluble BrC contributes 23 % of total absorption at 660 nm.
Qun He, Zhaowen Wang, Houfeng Liu, Pengju Xu, Rongbao Duan, Caihong Xu, Jianmin Chen, and Min Wei
Atmos. Chem. Phys., 24, 12775–12792, https://doi.org/10.5194/acp-24-12775-2024, https://doi.org/10.5194/acp-24-12775-2024, 2024
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Coastal environments provide an ideal setting for investigating the intermixing of terrestrial and marine aerosols. Terrestrial air mass constituted a larger number of microbes from anthropogenic and soil emissions, whereas saprophytic and gut microbes were predominant in marine samples. Mixed air masses indicated a fusion of marine and terrestrial aerosols, characterized by alterations in the ratio of pathogenic and saprophytic microbes when compared to either terrestrial or marine samples.
Rime El Asmar, Zongrun Li, David J. Tanner, Yongtao Hu, Susan O'Neill, L. Gregory Huey, M. Talat Odman, and Rodney J. Weber
Atmos. Chem. Phys., 24, 12749–12773, https://doi.org/10.5194/acp-24-12749-2024, https://doi.org/10.5194/acp-24-12749-2024, 2024
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Prescribed burning is an important method for managing ecosystems and preventing wildfires. However, smoke from prescribed fires can have a significant impact on air quality. Here, using a network of fixed sites and sampling throughout an extended prescribed burning period in 2 different years, we characterize emissions and evolutions of up to 8 h of PM2.5 mass, black carbon (BC), and brown carbon (BrC) in smoke from burning of forested lands in the southeastern USA.
Matthew Boyer, Diego Aliaga, Lauriane L. J. Quéléver, Silvia Bucci, Hélène Angot, Lubna Dada, Benjamin Heutte, Lisa Beck, Marina Duetsch, Andreas Stohl, Ivo Beck, Tiia Laurila, Nina Sarnela, Roseline C. Thakur, Branka Miljevic, Markku Kulmala, Tuukka Petäjä, Mikko Sipilä, Julia Schmale, and Tuija Jokinen
Atmos. Chem. Phys., 24, 12595–12621, https://doi.org/10.5194/acp-24-12595-2024, https://doi.org/10.5194/acp-24-12595-2024, 2024
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We analyze the seasonal cycle and sources of gases that are relevant for the formation of aerosol particles in the central Arctic. Since theses gases can form new particles, they can influence Arctic climate. We show that the sources of these gases are associated with changes in the Arctic environment during the year, especially with respect to sea ice. Therefore, the concentration of these gases will likely change in the future as the Arctic continues to warm.
Binyu Xiao, Fan Zhang, Zeyu Liu, Yan Zhang, Rui Li, Can Wu, Xinyi Wan, Yi Wang, Yubao Chen, Yong Han, Min Cui, Libo Zhang, Yingjun Chen, and Gehui Wang
EGUsphere, https://doi.org/10.5194/egusphere-2024-3433, https://doi.org/10.5194/egusphere-2024-3433, 2024
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Intermediate/semi-volatile organic compounds in both gas and particle phases from ship exhausts are enhanced due to the switch of fuels from low-sulfur to ultra-low-sulfur. The findings indicate that optimization is necessary for the forthcoming global implementation of an ultra-low-sulfur oil policy. Besides, we find that organic diagnostic markers of hopanes, in conjunction with the ratio of octadecanoic to tetradecanoic could be considered as potential tracers for HFO exhausts.
Mutian Ma, Laura-Hélèna Rivellini, Yichen Zong, Markus Kraft, Liya E. Yu, and Alex King Yin Lee
EGUsphere, https://doi.org/10.5194/egusphere-2024-3240, https://doi.org/10.5194/egusphere-2024-3240, 2024
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This work advances our understanding of emission and atmospheric evolution of black carbon (BC) particles in Singapore, a complex urban environment impacted by multiple local and regional combustion sources, based on the improved source apportionment analysis of real-time aerosol mass spectrometry measurement.
Hongyu Zhang, Shenbo Wang, Zhangsen Dong, Xiao Li, and Ruiqin Zhang
EGUsphere, https://doi.org/10.5194/egusphere-2024-2869, https://doi.org/10.5194/egusphere-2024-2869, 2024
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To address this, 12-year observational data in Zhengzhou were investigated and revealed that the resuspension of surrounding soil dust determined the rebound of crustal material concentrations after 2019, further elevating the particle pH. Therefore, the future ammonia reduction policies in North China may not lead to a rapid increase in particle acidity buffering by the crustal materials, but it is necessary to consider synergistic control with dust sources.
Haley M. Royer, Michael T. Sheridan, Hope E. Elliott, Nurun Nahar Lata, Zezhen Cheng, Swarup China, Zihua Zhu, Andrew P. Ault, and Cassandra J. Gaston
EGUsphere, https://doi.org/10.5194/egusphere-2024-3288, https://doi.org/10.5194/egusphere-2024-3288, 2024
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Saharan dust transported across the Atlantic to the Caribbean, South America, and North America is hypothesized to undergo chemical processing by inorganic and organic acids that enhances cloud droplet formation, nutrient availability, and reflectivity of. 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.
Imad El Haddad, Danielle Vienneau, Kaspar R. Daellenbach, Robin Modini, Jay G. Slowik, Abhishek Upadhyay, Petros N. Vasilakos, David Bell, Kees de Hoogh, and Andre S. H. Prevot
Atmos. Chem. Phys., 24, 11981–12011, https://doi.org/10.5194/acp-24-11981-2024, https://doi.org/10.5194/acp-24-11981-2024, 2024
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This opinion paper explores how advances in aerosol science inform our understanding of the health impacts of outdoor particulate pollution. We advocate for a shift in the way we target PM pollution, focusing on the most harmful anthropogenic emissions. We highlight key observations, modelling developments, and emission measurements needed to achieve this shift.
Yu Huang, Xingru Li, Dan Dan Huang, Ruoyuan Lei, Binhuang Zhou, Yunjiang Zhang, and Xinlei Ge
EGUsphere, https://doi.org/10.5194/egusphere-2024-2757, https://doi.org/10.5194/egusphere-2024-2757, 2024
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This work performed a comprehensive investigation on the chemical and optical properties of the brown carbon in PM2.5 samples collected in Nanjing, China. In particular, we used the machine learning approach to identify a list of key BrC species, which can be a good reference for future studies. Our findings extend the understanding on BrC properties and are valuable to the assessment of its impact on air quality and radiative forcing.
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.
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.
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
EGUsphere, https://doi.org/10.5194/egusphere-2024-2604, https://doi.org/10.5194/egusphere-2024-2604, 2024
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Novel aerosol hygroscopicity analysis of CAMP2Ex 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.
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.
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
EGUsphere, https://doi.org/10.5194/egusphere-2024-2903, https://doi.org/10.5194/egusphere-2024-2903, 2024
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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, like ultra-fine particles, were higher in the port than in the city and offer a strong support to improve emission inventories. These findings may also serve as reference for assessing the benefits of a Sulphur Emission Control Area in the Mediterranean in 2025.
Cited articles
Aldahan, A., Possnert, G., Alfimov, V., and Cato, K.: Anthropogenic 129I
in the Baltic Sea, Nucl. Instrum. Meth. B, 259, 491–495, 2007.
Alfimov, V., Aldahan, A., Possnert, G., Kekli, A., and Meili, M.:
Concentrations of 129I along a transect from the North Atlantic to the
Baltic Sea, Nucl. Instrum. Meth. B, 223–224, 446–450, 2004a.
Alfimov, V., Aldahan, A., Possnert, G., and Winsor, P.: Anthropogenic
iodine-129 in seawater along a transect from the Norwegian coastal current to
the North Pole, Mar. Pollut. Bull., 49, 1097–1104, 2004b.
Bachhuber, H. and Bunzl, K.: Background levels of atmospheric deposition to
ground and temporal variations of 129I, 127I, 137Cs and
7Be in a rural area of Germany, J. Environ. Radioact., 16, 77–89, 1992.
Baker, A. R.: Inorganic iodine speciation in tropical Atlantic aerosol,
Geophys. Res. Lett., 31, L23S02, https://doi.org/10.1029/2004GL020144, 2004.
Baker, A. R.: Marine Aerosol Iodine Chemistry: The importance of soluble
organic iodine, Environ. Chem., 2, 295–298, 2005.
Baker, A. R., Tunnicliffe, C., and Jickells, T. D.: Iodine speciation and
deposition fluxes from the marine atmosphere, J. Geophys. Res., 106,
28743–28749, 2001.
Bewers, J. M. and Haysom, H. H.: The terrigenous dust contribution to
fluoride and iodide in atmospheric precipitation, J. Rech. Atmos., 8,
689–697, 1974.
Buesseler, K. O., Jayne, S. R., Fisher, N. S., Rypina, I. I., Baumann, H.,
Baumann, Z., Breier, C. F., Douglass, E. M., George, J., Macdonald, A. M.,
Miyamoto, H., Nishikawa, J., Pike, S. M., and Yoshida, S.: Fukushima-derived
radionuclides in the ocean and biota off Japan, P. Natl. Acad. Sci. USA, 109,
5984–5988, 2012.
Buraglio, N., Aldahan, A., and Possnert, G.: Distribution and inventory of
129I in the central Arctic Ocean, Geophys. Res. Lett., 26, 1011–1014,
1999.
Carpenter, L. J.: Iodine in the Marine Boundary Layer, Chem. Rev., 103,
4953–4962, 2003.
Chatfield, R. B. and Crutzen, P. J.: Are there interactions of iodine and
sulfur species in marine air photochemistry?, J. Geophys. Res.-Atmos., 95,
22319–22341, 1990.
Christl, M., Casacuberta, N., Lachner, J., Maxeiner, S., Vockenhuber, C.,
Synal, H.-A., Gorncy, I., Herrmann, J., Daraoui, A., Walther, C., and Michel,
R.: Status of 236U analyses at ETH Zurich and the distribution of
236U and 129I in the North Sea in 2009, Nucl. Instrum. Meth. B, 36,
510–516, 2015.
Clemenza, M., Fiorini, E., Previtali, E., and Sala, E.: Measurement of
airborne 131I, 134Cs and 137Cs due to the Fukushima reactor
incident in Milan (Italy), J. Environ. Radioactiv., 114, 113–118, 2012.
Daraoui, A., Michel, R., Gorny, M., Jakob, D., Sachse, R., Synal, H.-A., and
Alfimov, V.: Iodine-129, iodine-127 and caesium-137 in the environment: soil
from Germany and Chile, J. Environ. Radioactiv., 112, 8–22, 2012.
Englund, E., Aldahan, A., Hou, X., Petersen, R., and Possnert, G.: Speciation
of iodine (I-127 and I-129) in lake sediments, Nucl. Instrum. Meth. B, 268,
1102–1105, 2010a.
Englund, E., Aldahan, A., Hou, X., Possnert, G., and Soderstrom, C.: Iodine
(I-129 and I-127) in aerosols from northern Europe, Nucl. Instrum. Meth. B,
268, 1139–1141, 2010b.
Ernst, T., Szidat, S., Handl, J., Jakob, D., Michel, R., Schnabel, C., Synal,
H. A., Arevalo, F. J., Benne, I., Boess, J., Gehrt, E., Capelle, A.,
Schneider, J., Schafer, W., and Bottcher, J.: Migration of iodine-129 and
iodine-127 in soils, Kerntechnik (Germany), 68, 155–167, 2003.
Ezerinskis, Z., Hou, X. L., Druteikiene, R., Puzas, A., Sapolaite, J.,
Gvozdaite, R., Gudelis, A., Buivydas, S., and Remeikis, V.: Distribution and
source of 129I, 239, 240Pu, 137Cs in the environment of
Lithuania, J. Environ. Radioactiv., 151, 166–173, 2016.
Feczko, T., Puxbaum, H., Kasper-Giebl, A., Handler, M., Limbeck, A.,
Gelencsér, A., Pio, C., Preunkert, S., and Legrand, M.: Determination of
water and alkaline extractable atmospheric humic-like substances with the TU
Vienna HULIS analyzer in samples from six background sites in Europe, J.
Geophys. Res.-Atmos., 112, 1–9, 2007.
Gabler, H. E. and Heumann, K. G.: Determination of particulate iodine in
aerosols from different regions by size fractionating impactor sampling and
IDMS, Intern. J. Anal. Chem., 50, 129–146, 1993.
Galloway, J. N.: Acid deposition-perspectives in time and space, Water Air
Soil Poll., 85, 15–24, 1995.
Gilfedder, B. S., Lai, S. C., Petri, M., Biester, H., and Hoffmann, T.:
Iodine speciation in rain, snow and aerosols, Atmos. Chem. Phys., 8,
6069–6084, https://doi.org/10.5194/acp-8-6069-2008, 2008.
Gilfedder, B. S., Chance, R., Dettmann, U., Lai, S. C., and Baker, A. R.:
Determination of total and non-water soluble iodine in atmospheric aerosols
by thermal extraction and spectrometric detection (TESI), Anal. Bioanal.
Chem., 398, 519–526, 2010.
Havers, N., Burba, P., Lambert, J., and Klockow, D.: Spectroscopic
Characterization of Humic-Like Substances in Airborne Particulate Matter, J.
Atmos. Chem., 29, 45–54, 1998.
He, P., Hou, X., Aldahan, A., Possnert, G., and Yi, P.: Iodine isotopes
species fingerprinting environmental conditions in surface water along the
northeastern Atlantic Ocean, Scientific Reports, 3, 2685, 1–8, 2013.
He, P., Aldahan, A., Possnert, G., and Hou, X.: Temporal Variation of Iodine
Isotopes in the North Sea, Environ. Sci. Technol., 48, 1419–1425, 2014.
Hou, X., Fogh, C. L., Kucera, J., Andersson, K. G., Dahlgaard, H., and
Nielsen, S. P.: Iodine-129 and Caesium-137 in Chernobyl contaminated soil and
their chemical fractionation, Sci. Total Environ., 308, 97–109, 2003.
Hou, X., Aldahan, A., Nielsen, S. P., Possnert, G., Nies, H., and Hedfors,
J.: Speciation of I-129 and I-127 in seawater and implications for sources
and transport pathways in the North Sea, Environ. Sci. Technol., 41,
5993–5999, 2007.
Hou, X., Aldahan, A., Nielsen, S. P., and Possnert, G.: Time series of I-129
and I-127 Speciation in precipitation from Denmark, Environ. Sci. Technol.,
43, 6522–6528, 2009a.
Hou, X., Hansen, V., Aldahan, A., Possnert, G., Lind, O. C., and
Lujanienė, G.: A review on speciation of iodine-129 in the environmental
and biological samples, Anal. Chim. Acta, 632, 181–196, 2009b.
Hou, X., Povinec, P. P., Zhang, L., Shi, K., Biddulph, D., Chang, C., Fan,
Y., Ješkovský, M., Liu, Q., Luo, M., Steier, P., Zhou, W. J., Hou,
Y., and Golser, R.: Iodine-129 in Seawater Offshore Fukushima: Distribution,
Inorganic Speciation, Sources, and Budget, Environ. Sci. Technol., 47,
3091–3098, 2013.
Jabbar, T., Steier, P., Wallner, G., Kandler, N., and Katzlberger, C.: AMS
analysis of iodine-129 in aerosols from Austria, Nucl. Instrum. Meth. B, 269,
3183–3187, 2011.
Jabbar, T., Steier, P., Wallner, G., Priller, A., Kandler, N., and Kaiser,
A.: Iodine Isotopes (127I and 129I) in Aerosols at High Altitude
Alp Stations, Environ. Sci. Technol., 46, 8637–8644, 2012.
Krupp G. and Aumann D. C.: Iodine-129 in rainfall over Germany, J. Environ.
Radiat., 46, 287–299, 1999.
Leon, J. D., Jaffe, D. A., Kaspar, J., Knecht, A., Miller, M. L., Robertson,
R. G. H., and Schubert, A. G.: Arrival time and magnitude of airborne fission
products from the Fukushima, Japan, reactor incident as measured in Seattle,
WA, USA, J. Environ. Radioactiv., 102, 1032–1038, 2011.
Lindberg, S. E., Brooks, S., Lin, C., Scott, K. J., Landis, M. S., Stevens,
R. K., Goodsite, M., and Richter, A.: Dynamic Oxidation of Gaseous Mercury in
the Arctic Troposphere at Polar Sunrise, Environ. Sci. Technol., 36,
1245–1256, 2002.
Lopez-Gutierrez, J. M., Santos, F. J., Garcia-Leon, M., Schnabel, Ch., Synal,
H.-A., Ernst, Th., and Szidat, S.: Levels and temporal variability of
129I concentrations and 129I/127I isotopic ratios in
atmospheric samples from southern Spain, Nucl. Instrum. Meth. B, 223–224,
495–500, 2004.
Manolopoulou, M., Vagena, E., Stoulos, S., Ioannidou, A., and Papastefanou,
C.: Radioiodine and radiocesium in Thessaloniki, Northern Greece due to the
Fukushima nuclear accident, J. Environ. Radioactiv., 102, 796–797, 2011.
McFiggans, G., Plane, J. M. C., Allan, B. J., Carpenter, L. J., Coe, H., and
O'Dowd, C.: A modeling study of iodine chemistry in the marine boundary
layer, J. Geophys. Res.-Atmos., 105, 14371–14385, 2000.
Michel, R., Daraoui, A., Gorny, M., Jakob, D., Sachse, R., Tosch, L., Nies,
H., Goroncy, I., Herrmann, J., Synal, H. A., Stocker, M., and Alfimov, V.:
Iodine-129 and iodine-127 in European seawaters and in precipitation from
Northern Germany, Sci. Total Environ., 419, 151–169, 2012.
Muramatsu, Y., Matsuzaki, H., Toyama, C., and Ohno, T.: Analysis of 129I
in the soils of Fukushima Prefecture: preliminary reconstruction of 131I
deposition related to the accident at Fukushima Daiichi Nuclear Power Plant
(FDNPP), J. Environ. Radioactiv., 139, 344–350, 2015.
Nielsen, S. P., Anderson, K. P., and Miller, A.: December 2011Radioactivity
in the Risø District January–June 2011, Risø Report,
Risø-R-1800(EN), 2011.
O'Dowd, C. D., Facchini, M. C., Cavalli, F., Ceburnis, D., Mircea, M.,
Decesari, S., Fuzzi, S., Yoon, Y. J., and Putaud, J.: Biogenically driven
organic contribution to marine aerosol, Nature, 431, 676–680, 2004.
O'Dowd, C. D., Jimenez, J. L., Bahreini, R., Flagan, R. C., Seinfeld, J. H.,
Hämeri, K., Pirjola, L., Kulmala, M., Jennings, S. G., and Hoffmann, T.:
Marine aerosol formation from biogenic iodine emissions, Nature, 417,
632–636, 2002.
Osterc, A. and Stibilj, V.: 129I level in soil from Ukraine and Slovenia
in the last decade, Intern. J. Environ. Anal. Chem., 93, 553–564, 2013.
Pechtl, S., Schmitz, G., and von Glasow, R.: Modelling iodide – iodate
speciation in atmospheric aerosol: Contributions of inorganic and organic
iodine chemistry, Atmos. Chem. Phys., 7, 1381–1393,
https://doi.org/10.5194/acp-7-1381-2007, 2007.
Persson, S., Aldahan, A., Possnert, G., Alfimov, V., and Hou, X.: 129I
Variability in precipitation over Europe, Nucl. Instrum. Meth. B, 259,
508–512, 2007.
Pittauerová, D., Hettwig, B., and Fischer, H. W.: Fukushima fallout in
Northwest German environmental media, J. Environ. Radioactiv., 102, 877–880,
2011.
Prados-Roman, C., Cuevas, C. A., Hay, T., Fernandez, R. P., Mahajan, A. S.,
Royer, S.-J., Galí, M., Simó, R., Dachs, J., Großmann, K.,
Kinnison, D. E., Lamarque, J.-F., and Saiz-Lopez, A.: Iodine oxide in the
global marine boundary layer, Atmos. Chem. Phys., 15, 583–593,
https://doi.org/10.5194/acp-15-583-2015, 2015.
Qiao, J., Hansen, V., Hou, X., Aldahan, A., and Possnert, G.: Speciation
analysis of 129I, 137Cs, 232Th, 238U, 239Pu and
240Pu in environmental soil and sediment, Appl. Radial. Isot., 70,
1698–1708, 2012.
Quinn, P. K., Bates, T. S., Schulz, K. S., Coffman, D. J., Frossard, A. A.,
Russell, L. M., Keene, W. C., and Kieber, D. J.: Contribution of sea surface
carbon pool to organic matter enrichment in sea spray aerosol, Nat. Geosci.,
7, 228–232, 2014.
Raisbeck, G. M., Yiou, F., Zhou, Z. Q., and Kilius, L. R.: 129I from
nuclear fuel reprocessing facilities at Sellafield (U.K.) and La Hague
(France); potential as an oceanographic tracer, J. Mar. Syst., 6, 561–570,
1995.
Reithmeier, H., Lazarev, V., Ruhm, W., Schwikowski, M., Gaggeler, H. W., and
Nolte, E.: Estimate of European 129I releases supported by 129I
analysis in an alpine ice core, Environ. Sci. Technol., 40, 5891–5896, 2006.
Reithmeier, H., Lazarev, V., Rühm, W., and Nolte, E.: Anthropogenic
129I in the atmosphere: Overview over major sources, transport processes
and deposition pattern, Sci. Total Environ., 408, 5052–5064, 2010.
Saiz-Lopez, A. and Plane, J. M. C.: Novel iodine chemistry in the marine
boundary layer, Geophys. Res. Lett., 31, L04112, https://doi.org/10.1029/2003GL019215,
2004.
Saiz-Lopez, A., Gómez Martín, J. C., Plane, J. M. C., Saunders, R.
W., Baker, A. R., Von Glasow, R., Carpenter, L. J., and McFiggans, G.:
Atmospheric chemistry of iodine, Chem. Rev., 112, 1773–1804, 2012.
Santos, F. J., López-Gutiérrez, J. M., García-León, M.,
Suter, M., and Synal, H. A.: Determination of 129I/127I in aerosol
samples in Seville (Spain), J. Environ. Radioactiv., 84, 103–109, 2005.
Schnabel, C., Lopez-Gutierrez, J. M., Szidat, S., Sprenger, M., Wernli, H.,
Beer, J., and Synal, H.-A.: On the origin of 129I in rain water near
Zürich, Radiochim. Acta, 89, 815–822, 2001.
Simpson, W. R., von Glasow, R., Riedel, K., Anderson, P., Ariya, P.,
Bottenheim, J., Burrows, J., Carpenter, L. J., Frieß, U., Goodsite, M.
E., Heard, D., Hutterli, M., Jacobi, H.-W., Kaleschke, L., Neff, B., Plane,
J., Platt, U., Richter, A., Roscoe, H., Sander, R., Shepson, P., Sodeau, J.,
Steffen, A., Wagner, T., and Wolff, E.: Halogens and their role in polar
boundary-layer ozone depletion, Atmos. Chem. Phys., 7, 4375–4418,
https://doi.org/10.5194/acp-7-4375-2007, 2007.
Szidat, S., Schmidt, A., Handl, J., Jakob, D., Botsch, W., Michel, R., Synal,
H. A., Schnabel, C., Suter, M., López-Gutiérrez, J. M., and Stade,
W.: Iodine-129: Sample preparation, quality control and analyses of
pre-nuclear materials and of natural waters from Lower Saxony, Germany, Nucl.
Instrum. Meth. B, 172, 699–710, 2000.
Toyama, C., Muramatsu, Y., Igarashi, Y., Aoyama, M., and Matsuzaki, H.:
Atmospheric fallout of 129I in Japan before the Fukushima accident:
regional and global contributions (1963–2005), Environ. Sci. Technol., 47,
8383–8390, 2013.
Tölgyessy, J. (Ed.): Chemistry and Biology of Water, Air and
Soil-Environmental Aspects, Studies in Environmental Science, Elsevier,
Amsterdam-London-New York-Tokyo, 53, 1–858, 1993.
Tsukada, H., Hara, H., Iwashima, K., and Yamagata, N.: The iodine content of
atmospheric aerosols as determined by the use of a fluoropore filter for
collection, B. Chem. Soc. Jpn., 60, 3195–3198, 1987.
Vogt, R., Sander, R., von Glasow, R., and Crutzen, P.: Iodine Chemistry and
its Role in Halogen Activation and Ozone Loss in the Marine Boundary Layer: A
Model Study, J. Atmos. Chem., 32, 375–395, 1999.
Weather Wunderground: available at: http://www.wunderground.com/, last
access: 26 May 2015.
Wimschneider, A. and Heumann, K. G.: Iodine speciation in size fractionated
atmospheric particles by isotope dilution mass spectrometry, Fresenius J.
Anal. Chem., 353, 191–196, 1995.
Xu, S., Freeman, S. P. H. T., Hou, X., Watanabe, A., Yamaguchi, K., and
Zhang, L.: Iodine Isotopes in Precipitation: Temporal Responses to 129I
Emissions from the Fukushima Nuclear Accident, Environ. Sci. Technol., 47,
10851–10859, 2013.
Xu, S., Zhang, L., Freeman, S. P. H. T., Hou, X., Shibata, Y., Sanderson, D.,
Cresswell, A., Doi, T., and Tanaka, A.: Speciation of Radiocesium and
Radioiodine in Aerosols from Tsukuba after the Fukushima Nuclear Accident,
Environ. Sci. Technol., 49, 1017–1024, 2015.
Yi, P., Aldahan, A., Hansen, V., Possnert, G., and Hou, X.: Iodine Isotopes
(129I and 127I) in the Baltic Proper, Kattegat, and Skagerrak
Basins, Environ. Sci. Technol., 43, 903–909, 2011.
Yi, P., Aldahan, A., Possnert, G., Hou, X., Hansen, V., and Wang, B.:
127I and 129I Species and Transformation in the Baltic Proper,
Kattegat, and Skagerrak Basins, Environ. Sci. Technol., 46, 10948–10956,
2012.
Zhang, L., Hou, X., and Xu, S.: Speciation Analysis of 129I and
127I in Aerosols Using Sequential Extraction and Mass Spectrometry
Detection, Anal. Chem., 87, 6937–6944, 2015.
Zhang, L., Zhou, W., Hou, X., Chen, N., Liu, Q., He, C., Fan, Y., Luo, M.,
Wang, Z., and Fu, Y.: Level and source of 129I of environmental samples
in Xi'an region, China. Sci. Total Environ., 409, 3780–3788, 2011.
Short summary
Speciation analysis of long-lived anthropogenic iodine isotopes (129I) in time series Danish aerosols shows that secondary emission from heavily 129I-contaminated seawater is a major source of 129I in the Atmosphere, at least in North Europe. Iodide is the major form of water-soluble iodine, while NaOH-soluble iodine is the dominant species of iodine in aerosol, which is likely bound with organic substances. The contribution of Fukushima-derived 129I is estimated to be negligible in Europe.
Speciation analysis of long-lived anthropogenic iodine isotopes (129I) in time series Danish...
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