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IF5.414
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5.958
5.958
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9.7
9.7
SNIP1.517
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Abstracted/indexed
Abstracted/indexedSpecial issue
Short summary
Our study presents an analysis of the vertical and horizontal black carbon properties across northern India using aircraft measurements. The Indo-Gangetic Plain saw the greatest black carbon mass concentrations during the pre-monsoon season. Two black carbon modes were recorded: a small black carbon mode (traffic emissions) in the north-west and a moderately coated mode (solid-fuel emissions) in the Indo-Gangetic Plain. In the vertical profile, absorption properties increase with height.
Our study presents an analysis of the vertical and horizontal black carbon properties across...
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ACP | Articles | Volume 19, issue 20
Atmos. Chem. Phys., 19, 13079–13096, 2019
https://doi.org/10.5194/acp-19-13079-2019
© Author(s) 2019. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Special issue: Interactions between aerosols and the South West Asian...
Atmos. Chem. Phys., 19, 13079–13096, 2019
https://doi.org/10.5194/acp-19-13079-2019
© Author(s) 2019. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Research article 23 Oct 2019
Research article | 23 Oct 2019
Black carbon physical and optical properties across northern India during pre-monsoon and monsoon seasons
James Brooks et al.
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Huihui Wu, Jonathan W. Taylor, Kate Szpek, Justin M. Langridge, Paul I. Williams, Michael Flynn, James D. Allan, Steven J. Abel, Joseph Pitt, Michael I. Cotterell, Cathryn Fox, Nicholas W. Davies, Jim Haywood, and Hugh Coe
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Nils Friedrich, Ivan Tadic, Jan Schuladen, James Brooks, Eoghan Darbyshire, Frank Drewnick, Horst Fischer, Jos Lelieveld, and John N. Crowley
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Lei Liu, Jian Zhang, Yinxiao Zhang, Yuanyuan Wang, Liang Xu, Qi Yuan, Dantong Liu, Yele Sun, Pingqing Fu, Zongbo Shi, and Weijun Li
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2020-1012, https://doi.org/10.5194/acp-2020-1012, 2020
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Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2020-890, https://doi.org/10.5194/acp-2020-890, 2020
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We are presenting a new method to apportion Black Carbon/soot into multiple sources through the inclusion of fullerene and metal data into SP-AMS factorisation. While this is itself would be considered a technical development, we can present a budget of contributions to measured BC during the event studied, including the conclusion that fireworks contributed little compared to the bonfire, traffic and domestic wood burning emissions.
Sobhan Kumar Kompalli, Surendran Nair Suresh Babu, Krishnaswamy Krishnamoorthy, Sreedharan Krishnakumari Satheesh, Mukunda M. Gogoi, Vijayakumar S. Nair, Jayachandran V, Dantong Liu, Michael Flynn, and Hugh Coe
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Jonathan W. Taylor, Huihui Wu, Kate Szpek, Keith Bower, Ian Crawford, Michael J. Flynn, Paul I. Williams, James Dorsey, Justin M. Langridge, Michael I. Cotterell, Cathryn Fox, Nicholas W. Davies, Jim M. Haywood, and Hugh Coe
Atmos. Chem. Phys., 20, 11201–11221, https://doi.org/10.5194/acp-20-11201-2020, https://doi.org/10.5194/acp-20-11201-2020, 2020
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Every year, huge plumes of smoke hundreds of miles wide travel over the south Atlantic Ocean from fires in central and southern Africa. These plumes absorb the sun’s energy and warm the climate. We used airborne optical instrumentation to determine how absorbing the smoke was as well as the relative importance of black and brown carbon. We also tested different ways of simulating these properties that could be used in a climate model.
Archit Mehra, Jordan E. Krechmer, Andrew Lambe, Chinmoy Sarkar, Leah Williams, Farzaneh Khalaj, Alex Guenther, John Jayne, Hugh Coe, Douglas Worsnop, Celia Faiola, and Manjula Canagaratna
Atmos. Chem. Phys., 20, 10953–10965, https://doi.org/10.5194/acp-20-10953-2020, https://doi.org/10.5194/acp-20-10953-2020, 2020
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Emissions of volatile organic compounds (VOCs) from plants are important for tropospheric ozone and secondary organic aerosol (SOA) formation. Real plant emissions are much more diverse than the few proxies widely used for studies of plant SOA. Here we present the first study of SOA from Californian sage plants and the oxygenated monoterpenes representing their major emissions. We identify SOA products and show the importance of the formation of highly oxygenated organic molecules and oligomers.
Lisa K. Whalley, Eloise J. Slater, Robert Woodward-Massey, Chunxiang Ye, James D. Lee, Freya Squires, James R. Hopkins, Rachel E. Dunmore, Marvin Shaw, Jacqueline F. Hamilton, Alastair C. Lewis, Archit Mehra, Stephen D. Worrall, Asan Bacak, Thomas J. Bannan, Hugh Coe, Bin Ouyang, Roderic L. Jones, Leigh R. Crilley, Louisa J. Kramer, William J. Bloss, Tuan Vu, Simone Kotthaus, Sue Grimmond, Yele Sun, Weiqi Xu, Siyao Yue, Lujie Ren, W. Joe F. Acton, C. Nicholas Hewitt, Xinming Wang, Pingqing Fu, and Dwayne E. Heard
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2020-785, https://doi.org/10.5194/acp-2020-785, 2020
Revised manuscript accepted for ACP
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To understand how emission controls will impact ozone, an understanding of the sources and sinks of OH and the chemical cycling between peroxy radicals is needed. This paper presents measurements of OH, HO2, and total RO2 taken in central Beijing. The radical observations are compared to a detailed chemistry model which shows that under low NO conditions there is a missing OH source. Under high NOx conditions, the model under-predicts RO2 and impacts our ability to model ozone.
Ernesto Reyes-Villegas, Upasana Panda, Eoghan Darbyshire, James M. Cash, Rutambhara Joshi, Ben Langford, Chiara F. Di Marco, Neil Mullinger, W. Joe F. Acton, Will Drysdale, Eiko Nemitz, Michael Flynn, Aristeidis Voliotis, Gordon McFiggans, Hugh Coe, James Lee, C. Nicholas Hewitt, Mathew R. Heal, Sachin S. Gunthe, Shivani, Ranu Gadi, Siddhartha Singh, Vijay Soni, and James D. Allan
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2020-894, https://doi.org/10.5194/acp-2020-894, 2020
Preprint under review for ACP
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David Topping, David Watts, Hugh Coe, James Evans, Thomas J. Bannan, Douglas Lowe, Caroline Jay, and Jonathan W. Taylor
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Preprint under review for GMD
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Time-series forecasting methods have often been used to mitigate some of the challenges associated with deploying chemical transport models. In this study we deploy and evaluate Facebook’s Prophetmodel v0.6 in predicting hourly concentrations of Nitrogen Dioxide [NO2]. et. Overall we find the Prophet model offers a relatively effective and simple way to make predictions about NO2 at local levels.
Ben Kravitz, Douglas G. MacMartin, Daniele Visioni, Olivier Boucher, Jason N. S. Cole, Jim Haywood, Andy Jones, Thibaut Lurton, Pierre Nabat, Ulrike Niemeier, Alan Robock, Roland Séférian, and Simone Tilmes
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2020-732, https://doi.org/10.5194/acp-2020-732, 2020
Revised manuscript under review for ACP
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This study investigates multi-model response to idealized geoengineering (high CO2 with solar reduction) across two different generations of climate models. We find that except in a few cases, the results are unchanged between the different generations. This gives us confidence that broad conclusions about the response to idealized geoengineering are robust.
Archit Mehra, Yuwei Wang, Jordan E. Krechmer, Andrew Lambe, Francesca Majluf, Melissa A. Morris, Michael Priestley, Thomas J. Bannan, Daniel J. Bryant, Kelly L. Pereira, Jacqueline F. Hamilton, Andrew R. Rickard, Mike J. Newland, Harald Stark, Philip Croteau, John T. Jayne, Douglas R. Worsnop, Manjula R. Canagaratna, Lin Wang, and Hugh Coe
Atmos. Chem. Phys., 20, 9783–9803, https://doi.org/10.5194/acp-20-9783-2020, https://doi.org/10.5194/acp-20-9783-2020, 2020
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Aromatic volatile organic compounds (VOCs) emitted from anthropogenic activity are important for tropospheric ozone and secondary organic aerosol (SOA) formation. Here we present a detailed chemical characterisation of SOA from four C9-aromatic isomers and a polycyclic aromatic hydrocarbon (PAH). We identify and compare their oxidation products in the gas and particle phases, showing the different relative importance of oxidation pathways and proportions of highly oxygenated organic molecules.
Jim M. Haywood, Steven J. Abel, Paul A. Barrett, Nicolas Bellouin, Alan Blyth, Keith N. Bower, Melissa Brooks, Ken Carslaw, Haochi Che, Hugh Coe, Michael I. Cotterell, Ian Crawford, Zhiqiang Cui, Nicholas Davies, Beth Dingley, Paul Field, Paola Formenti, Hamish Gordon, Martin de Graaf, Ross Herbert, Ben Johnson, Anthony C. Jones, Justin M. Langridge, Florent Malavelle, Daniel G. Partridge, Fanny Peers, Jens Redemann, Philip Stier, Kate Szpek, Jonathan W. Taylor, Duncan Watson-Parris, Robert Wood, Huihui Wu, and Paquita Zuidema
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2020-729, https://doi.org/10.5194/acp-2020-729, 2020
Revised manuscript accepted for ACP
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Every year, the seasonal cycle of biomass burning from agricultural practices in Africa creates a huge plume of smoke that travels many thousands of kilometres over the Atlantic Ocean. This study provides an overview of a measurement campaign called the CLoud-Aerosol-Radiation Interaction and Forcing: Year 2017 (CLARIFY-2017) and documents the rationale, deployment strategy, observations and key results from the campaign which utilised the heavily equipped FAAM atmospheric research aircraft.
Michael Priestley, Thomas J. Bannan, Michael Le Breton, Stephen D. Worrall, Sungah Kang, Iida Pullinen, Sebastian Schmitt, Ralf Tillmann, Einhard Kleist, Defeng Zhao, Jürgen Wildt, Olga Garmash, Archit Mehra, Asan Bacak, Dudley E. Shallcross, Åsa Halquist, Mikael Ehn, Astrid Kiendler-Scharr, Thomas F. Mentel, Gordon McFiggans, Mattias Halquist, Hugh Coe, and Carl J. Percival
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2020-819, https://doi.org/10.5194/acp-2020-819, 2020
Revised manuscript accepted for ACP
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A significant fraction of emissions from human activity consists of aromatic hydrocarbons e.g. benzene, which oxidise to form new compounds important for particle growth. Characterisation of benzene oxidation products highlights the range of species produced as well as their chemical properties and contextualises them within relevant frameworks e.g. MCM. Cluster analysis of the oxidation product time series' distinguishes behaviours of CHON compounds that can aid identifying functionality.
Yuwei Wang, Archit Mehra, Jordan E. Krechmer, Gan Yang, Xiaoyu Hu, Yiqun Lu, Andrew Lambe, Manjula Canagaratna, Jianmin Chen, Douglas Worsnop, Hugh Coe, and Lin Wang
Atmos. Chem. Phys., 20, 9563–9579, https://doi.org/10.5194/acp-20-9563-2020, https://doi.org/10.5194/acp-20-9563-2020, 2020
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A series of OH-initiated oxidation experiments of trimethylbenzene were investigated in the absence and presence of NOx. Many C9 products with 1–11 oxygen atoms and C18 products presumably formed from dimerization of C9 peroxy radicals were observed, hinting at the extensive existence of autoxidation and accretion reaction pathways. The presence of NOx would suppress the formation of highly oxygenated C18 molecules and enhance the formation of organonitrates and even dinitrate compounds.
Jill S. Johnson, Leighton A. Regayre, Masaru Yoshioka, Kirsty J. Pringle, Steven T. Turnock, Jo Browse, David M. H. Sexton, John W. Rostron, Nick A. J. Schutgens, Daniel G. Partridge, Dantong Liu, James D. Allan, Hugh Coe, Aijun Ding, David D. Cohen, Armand Atanacio, Ville Vakkari, Eija Asmi, and Ken S. Carslaw
Atmos. Chem. Phys., 20, 9491–9524, https://doi.org/10.5194/acp-20-9491-2020, https://doi.org/10.5194/acp-20-9491-2020, 2020
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We use over 9000 monthly aggregated grid-box measurements of aerosol to constrain the uncertainty in the HadGEM3-UKCA climate model. Measurements of AOD, PM2.5, particle number concentrations, sulfate and organic mass concentrations are compared to 1 million
variantsof the model using an implausibility metric. Despite many compensating effects in the model, the procedure constrains the probability distributions of many parameters, and direct radiative forcing uncertainty is reduced by 34 %.
Gunnar Myhre, Bjørn H. Samset, Christian W. Mohr, Kari Alterskjær, Yves Balkanski, Nicolas Bellouin, Mian Chin, James Haywood, Øivind Hodnebrog, Stefan Kinne, Guangxing Lin, Marianne T. Lund, Joyce E. Penner, Michael Schulz, Nick Schutgens, Ragnhild B. Skeie, Philip Stier, Toshihiko Takemura, and Kai Zhang
Atmos. Chem. Phys., 20, 8855–8865, https://doi.org/10.5194/acp-20-8855-2020, https://doi.org/10.5194/acp-20-8855-2020, 2020
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The radiative forcing of the direct aerosol effects can be decomposed into clear-sky and cloudy-sky portions. In this study we use observational methods and two sets of multi-model global aerosol simulations over the industrial era to show that the contribution from cloudy-sky regions is likely weak.
Mukunda Madhab Gogoi, Venugopalan Nair Jayachandran, Aditya Vaishya, Surendran Nair Suresh Babu, Sreedharan Krishnakumari Satheesh, and Krishnaswamy Krishna Moorthy
Atmos. Chem. Phys., 20, 8593–8610, https://doi.org/10.5194/acp-20-8593-2020, https://doi.org/10.5194/acp-20-8593-2020, 2020
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Extensive airborne measurements of aerosol number–size distribution and black carbon (BC) profiles are carried out for the first time across the IGP prior to the onset of the Indian summer monsoon. These measurements, combined with spaceborne sensors and model results, provided an east–west transect of the role of mineral dust (local and transported) in the aerosol loading across the IGP, with an increase in coarse mode concentration and coarse mode mass fraction with altitude.
Daniel J. Bryant, William J. Dixon, James R. Hopkins, Rachel E. Dunmore, Kelly L. Pereira, Marvin Shaw, Freya A. Squires, Thomas J. Bannan, Archit Mehra, Stephen D. Worrall, Asan Bacak, Hugh Coe, Carl J. Percival, Lisa K. Whalley, Dwayne E. Heard, Eloise J. Slater, Bin Ouyang, Tianqu Cui, Jason D. Surratt, Di Liu, Zongbo Shi, Roy Harrison, Yele Sun, Weiqi Xu, Alastair C. Lewis, James D. Lee, Andrew R. Rickard, and Jacqueline F. Hamilton
Atmos. Chem. Phys., 20, 7531–7552, https://doi.org/10.5194/acp-20-7531-2020, https://doi.org/10.5194/acp-20-7531-2020, 2020
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Using the chemical composition of offline filter samples, we report that a large share of oxidized organic aerosol in Beijing during summer is due to isoprene secondary organic aerosol (iSOA). iSOA organosulfates showed a strong correlation with the product of ozone and particulate sulfate. This highlights the role of both photochemistry and the availability of particulate sulfate in heterogeneous reactions and further demonstrates that iSOA formation is controlled by anthropogenic emissions.
Hang Liu, Xiaole Pan, Dantong Liu, Xiaoyong Liu, Xueshun Chen, Yu Tian, Yele Sun, Pingqing Fu, and Zifa Wang
Atmos. Chem. Phys., 20, 5771–5785, https://doi.org/10.5194/acp-20-5771-2020, https://doi.org/10.5194/acp-20-5771-2020, 2020
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The bare black carbon (BC) was in a fractal structure. With coating thickness increasing, BC changed from a fractal structure to a core–shell structure. In the ambient atmosphere, plenty of BC particles were not in a perfect core–shell structure. This study brought attention to the combined effects of morphology and coating thickness on the absorption enhancement of BC-containing particles, which is helpful for determining the climatic effects of BC.
Jian Zhang, Lei Liu, Liang Xu, Qiuhan Lin, Hujia Zhao, Zhibin Wang, Song Guo, Min Hu, Dantong Liu, Zongbo Shi, Dao Huang, and Weijun Li
Atmos. Chem. Phys., 20, 5355–5372, https://doi.org/10.5194/acp-20-5355-2020, https://doi.org/10.5194/acp-20-5355-2020, 2020
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Northeast China faces severe air pollution in regional haze in wintertime. In this study, we revealed a contrasting formation mechanism of two typical haze events: Haze-I was induced by adverse meteorological conditions together with residential coal burning emissions; Haze-II was caused by agricultural biomass waste burning. In particular, we observed large numbers of tar balls as the primary brown carbon in northeast China.
William T. Morgan, James D. Allan, Stéphane Bauguitte, Eoghan Darbyshire, Michael J. Flynn, James Lee, Dantong Liu, Ben Johnson, Jim Haywood, Karla M. Longo, Paulo E. Artaxo, and Hugh Coe
Atmos. Chem. Phys., 20, 5309–5326, https://doi.org/10.5194/acp-20-5309-2020, https://doi.org/10.5194/acp-20-5309-2020, 2020
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We flew a large atmospheric research aircraft across a number of different environments in the Amazon basin during the 2012 biomass burning season. Smoke from fires builds up and has a significant impact on weather, climate, health and natural ecosystems. Our goal was to quantify changes in the properties of the smoke emitted by fires as it is transported through the atmosphere. We found that the major control on the properties of the smoke was due to differences in the fires themselves.
Siddika Celik, Frank Drewnick, Friederike Fachinger, James Brooks, Eoghan Darbyshire, Hugh Coe, Jean-Daniel Paris, Philipp G. Eger, Jan Schuladen, Ivan Tadic, Nils Friedrich, Dirk Dienhart, Bettina Hottmann, Horst Fischer, John N. Crowley, Hartwig Harder, and Stephan Borrmann
Atmos. Chem. Phys., 20, 4713–4734, https://doi.org/10.5194/acp-20-4713-2020, https://doi.org/10.5194/acp-20-4713-2020, 2020
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Analysis of 252 ship emission plumes in the Mediterranean Sea and around the Arabian Peninsula examined particulate- and gas-phase characteristics. By identifying the corresponding ships, source features and plume age were determined. Emission factors (amount of pollutant per kilogram of fuel burned) were calculated and investigated for dependencies on source characteristics, atmospheric conditions, and transport time, providing insight into the most relevant influences on ship emissions.
Sobhan Kumar Kompalli, Surendran Nair Suresh Babu, Sreedharan Krishnakumari Satheesh, Krishnaswamy Krishna Moorthy, Trupti Das, Ramasamy Boopathy, Dantong Liu, Eoghan Darbyshire, James D. Allan, James Brooks, Michael J. Flynn, and Hugh Coe
Atmos. Chem. Phys., 20, 3965–3985, https://doi.org/10.5194/acp-20-3965-2020, https://doi.org/10.5194/acp-20-3965-2020, 2020
Mohanan R. Manoj, Sreedharan K. Satheesh, Krishnaswamy K. Moorthy, and Hugh Coe
Atmos. Chem. Phys., 20, 4031–4046, https://doi.org/10.5194/acp-20-4031-2020, https://doi.org/10.5194/acp-20-4031-2020, 2020
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The study reports the observation of highly absorbing aerosol layers at high altitudes (1–2.5 km) prior to monsoon and during its development over the Indian region and quantifies its climate impacts. The absorption of solar radiation in these layers perturbs the onset of monsoon through the impact on the atmospheric stability. When height-resolved values of single scattering albedo (SSA) are used in a radiative transfer model, a maximum heating ~1 K d (~twice that using SSA) is obtained.
Quan Liu, Dantong Liu, Qian Gao, Ping Tian, Fei Wang, Delong Zhao, Kai Bi, Yangzhou Wu, Shuo Ding, Kang Hu, Jiale Zhang, Deping Ding, and Chunsheng Zhao
Atmos. Chem. Phys., 20, 3931–3944, https://doi.org/10.5194/acp-20-3931-2020, https://doi.org/10.5194/acp-20-3931-2020, 2020
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We present a series of aircraft-based in situ measurements of aerosol chemical components and size distributions over the North China Plain, and the hygroscopicity is derived from aerosol chemical composition. These results reveal the vertical characteristics of aerosol hygroscopicity, and we investigated their impacts on optical properties and activation under different moisture and pollution conditions over this polluted region.
Gary Lloyd, Thomas Choularton, Keith Bower, Jonathan Crosier, Martin Gallagher, Michael Flynn, James Dorsey, Dantong Liu, Jonathan W. Taylor, Oliver Schlenczek, Jacob Fugal, Stephan Borrmann, Richard Cotton, Paul Field, and Alan Blyth
Atmos. Chem. Phys., 20, 3895–3904, https://doi.org/10.5194/acp-20-3895-2020, https://doi.org/10.5194/acp-20-3895-2020, 2020
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Measurements of liquid and ice cloud particles were made using an aircraft to penetrate fresh growing convective clouds in the tropical Atlantic. We found small ice particles at surprisingly high temperatures just below freezing. At colder temperatures secondary ice processes rapidly generated high concentrations of ice crystals.
Adil Shah, Joseph R. Pitt, Hugo Ricketts, J. Brian Leen, Paul I. Williams, Khristopher Kabbabe, Martin W. Gallagher, and Grant Allen
Atmos. Meas. Tech., 13, 1467–1484, https://doi.org/10.5194/amt-13-1467-2020, https://doi.org/10.5194/amt-13-1467-2020, 2020
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Methane is a potent greenhouse gas, with large flux uncertainties from facility-scale sources, such as natural gas extraction infrastructure. A recently developed flux quantification method was successfully tested by flying an unmanned aerial vehicle (UAV) downwind of 22 controlled atmospheric methane releases. The UAVs were used to derive high-precision atmospheric methane measurements. The UAV methodology was successful in both detecting the release and providing a rough flux estimate.
Chenjie Yu, Dantong Liu, Kurtis Broda, Rutambhara Joshi, Jason Olfert, Yele Sun, Pingqing Fu, Hugh Coe, and James D. Allan
Atmos. Chem. Phys., 20, 3645–3661, https://doi.org/10.5194/acp-20-3645-2020, https://doi.org/10.5194/acp-20-3645-2020, 2020
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This study presents the first atmospheric application of a new morphology-independent measurement for the quantification of the mixing state of rBC-containing particles in urban Beijing as part of the UK–China APHH campaign. An inversion method has been applied for better quantification of rBC mixing state. The mass-resolved rBC mixing state information presented here has implications for detailed models of BC, its optical properties and its atmospheric life cycle.
Vijayakumar S. Nair, Venugopalan Nair Jayachandran, Sobhan Kumar Kompalli, Mukunda M. Gogoi, and S. Suresh Babu
Atmos. Chem. Phys., 20, 3135–3149, https://doi.org/10.5194/acp-20-3135-2020, https://doi.org/10.5194/acp-20-3135-2020, 2020
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Extensive measurements of the aerosol and cloud condensation nuclei (CCN) properties in South Asian outflow to the northern Indian Ocean were carried out as a part of the ICARB-2018 experiment during winter. At high supersaturations, most of the aerosols in the South Asian outflow become activated as CCN, whereas the aerosol system over the equatorial Indian Ocean is less CCN efficient even at higher supersaturations.
Fanny Peers, Peter Francis, Steven J. Abel, Paul A. Barrett, Keith N. Bower, Michael I. Cotterell, Ian Crawford, Nicholas W. Davies, Cathryn Fox, Stuart Fox, Justin M. Langridge, Kerry G. Meyer, Steven E. Platnick, Kate Szpek, and Jim M. Haywood
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2019-1176, https://doi.org/10.5194/acp-2019-1176, 2020
Revised manuscript accepted for ACP
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Satellite observations at high temporal resolution are a valuable asset to monitor the transport of biomass burning plumes and the cloud diurnal cycle in the South Atlantic, but they need to be validated. Cloud and above-cloud aerosol properties retrieved from SEVIRI are compared against MODIS and measurements from the CLARIFY-2017 campaign. While some systematic differences are observed between SEVIRI and MODIS, the overall agreement in the cloud and aerosol properties is very satisfactory.
Sidhant J. Pai, Colette L. Heald, Jeffrey R. Pierce, Salvatore C. Farina, Eloise A. Marais, Jose L. Jimenez, Pedro Campuzano-Jost, Benjamin A. Nault, Ann M. Middlebrook, Hugh Coe, John E. Shilling, Roya Bahreini, Justin H. Dingle, and Kennedy Vu
Atmos. Chem. Phys., 20, 2637–2665, https://doi.org/10.5194/acp-20-2637-2020, https://doi.org/10.5194/acp-20-2637-2020, 2020
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Aerosols in the atmosphere have significant health and climate impacts. Organic aerosol (OA) accounts for a large fraction of the total aerosol burden, but models have historically struggled to accurately simulate it. This study compares two very different OA model schemes and evaluates them against a suite of globally distributed airborne measurements with the goal of providing insight into the strengths and weaknesses of each approach across different environments.
Ping Tian, Dantong Liu, Delong Zhao, Chenjie Yu, Quan Liu, Mengyu Huang, Zhaoze Deng, Liang Ran, Yunfei Wu, Shuo Ding, Kang Hu, Gang Zhao, Chunsheng Zhao, and Deping Ding
Atmos. Chem. Phys., 20, 2603–2622, https://doi.org/10.5194/acp-20-2603-2020, https://doi.org/10.5194/acp-20-2603-2020, 2020
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This study paints a full picture of the evolution of vertical characteristics of aerosol optical properties and shortwave heating impacts of carbonaceous aerosols during different stages of pollution events over the Beijing region and highlights the increased contribution of brown carbon absorption, especially at higher levels, during pollution.
Mike J. Newland, Daniel J. Bryant, Rachel E. Dunmore, Thomas J. Bannan, W. Joe F. Acton, Ben Langford, James R. Hopkins, Freya A. Squires, William Dixon, William S. Drysdale, Peter D. Ivatt, Mathew J. Evans, Peter M. Edwards, Lisa K. Whalley, Dwayne E. Heard, Eloise J. Slater, Robert Woodward-Massey, Chunxiang Ye, Archit Mehra, Stephen D. Worrall, Asan Bacak, Hugh Coe, Carl J. Percival, C. Nicholas Hewitt, James D. Lee, Tianqu Cui, Jason D. Surratt, Xinming Wang, Alastair C. Lewis, Andrew R. Rickard, and Jacqueline F. Hamilton
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2020-35, https://doi.org/10.5194/acp-2020-35, 2020
Revised manuscript accepted for ACP
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We report the formation of secondary pollutants in the urban Megacity of Beijing that are typically associated with remote regions such as rainforests. This is caused by extremely low levels of nitric oxide (NO), typically expected to be high in urban areas, observed in the afternoon. This work has significant implications for how we understand atmospheric chemistry in the urban environment, and thus how to implement effective policies to improve urban air quality.
Ross J. Herbert, Nicolas Bellouin, Ellie J. Highwood, and Adrian A. Hill
Atmos. Chem. Phys., 20, 1317–1340, https://doi.org/10.5194/acp-20-1317-2020, https://doi.org/10.5194/acp-20-1317-2020, 2020
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Marine stratocumulus clouds cover large regions of the ocean and act to cool the climate. We use high-resolution simulations to understand how observed layers of elevated smoke impact stratocumulus via the solar heating that occurs within the smoke layer. We find that the cloud response is strongest for thin, dense layers of smoke close to the cloud. The response rapidly weakens as the cloud-to-smoke gap increases. Generally, the smoke acts to thicken clouds and enhance their cooling effect.
Venugopalan Nair Jayachandran, Surendran Nair Suresh Babu, Aditya Vaishya, Mukunda M. Gogoi, Vijayakumar S. Nair, Sreedharan Krishnakumari Satheesh, and Krishnaswamy Krishna Moorthy
Atmos. Chem. Phys., 20, 561–576, https://doi.org/10.5194/acp-20-561-2020, https://doi.org/10.5194/acp-20-561-2020, 2020
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Concurrent measurements of the altitude profiles of the concentration of cloud condensation nuclei (CCNs), as a function of supersaturation (ranging from 0.2 % to 1.0 %), and aerosol optical properties were carried out aboard an instrumented aircraft across the Indo-Gangetic Plain (IGP) just prior to the onset of the 2016 Indian summer monsoon (ISM). A high CCN concentration is observed up to 2.5 km across the IGP, indicating the significant possibility of aerosol indirect effects.
Claire L. Ryder, Eleanor J. Highwood, Adrian Walser, Petra Seibert, Anne Philipp, and Bernadett Weinzierl
Atmos. Chem. Phys., 19, 15353–15376, https://doi.org/10.5194/acp-19-15353-2019, https://doi.org/10.5194/acp-19-15353-2019, 2019
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Mineral dust is lifted into the atmosphere from desert regions, where it can be transported over thousands of kilometres around the world. Dust impacts weather, climate, aviation, and air quality. We evaluate new aircraft observations of dust size. We find that the largest particles typically omitted by models have a significant impact on the interactions of dust with radiation and therefore climate. We also find that large dust particles are retained in the atmosphere longer than expected.
Sophie L. Haslett, Jonathan W. Taylor, Mathew Evans, Eleanor Morris, Bernhard Vogel, Alima Dajuma, Joel Brito, Anneke M. Batenburg, Stephan Borrmann, Johannes Schneider, Christiane Schulz, Cyrielle Denjean, Thierry Bourrianne, Peter Knippertz, Régis Dupuy, Alfons Schwarzenböck, Daniel Sauer, Cyrille Flamant, James Dorsey, Ian Crawford, and Hugh Coe
Atmos. Chem. Phys., 19, 15217–15234, https://doi.org/10.5194/acp-19-15217-2019, https://doi.org/10.5194/acp-19-15217-2019, 2019
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Three aircraft datasets from the DACCIWA campaign in summer 2016 are used here to show there is a background mass of pollution present in the lower atmosphere in southern West Africa. We suggest that this likely comes from biomass burning in central and southern Africa, which has been carried into the region over the Atlantic Ocean. This would have a negative health impact on populations living near the coast and may alter the impact of growing city emissions on cloud formation and the monsoon.
Leigh R. Crilley, Louisa J. Kramer, Bin Ouyang, Jun Duan, Wenqian Zhang, Shengrui Tong, Maofa Ge, Ke Tang, Min Qin, Pinhua Xie, Marvin D. Shaw, Alastair C. Lewis, Archit Mehra, Thomas J. Bannan, Stephen D. Worrall, Michael Priestley, Asan Bacak, Hugh Coe, James Allan, Carl J. Percival, Olalekan A. M. Popoola, Roderic L. Jones, and William J. Bloss
Atmos. Meas. Tech., 12, 6449–6463, https://doi.org/10.5194/amt-12-6449-2019, https://doi.org/10.5194/amt-12-6449-2019, 2019
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Nitrous acid (HONO) is key species for understanding tropospheric chemistry, yet accurate and precise measurements are challenging. Here we report an inter–comparison exercise of a number of instruments that measured HONO in a highly polluted location (Beijing). All instruments agreed on the temporal trends yet displayed divergence in absolute concentrations. The cause of this divergence was unclear, but it may in part be due to spatial variability in instrument location.
Philipp G. Eger, Nils Friedrich, Jan Schuladen, Justin Shenolikar, Horst Fischer, Ivan Tadic, Hartwig Harder, Monica Martinez, Roland Rohloff, Sebastian Tauer, Frank Drewnick, Friederike Fachinger, James Brooks, Eoghan Darbyshire, Jean Sciare, Michael Pikridas, Jos Lelieveld, and John N. Crowley
Atmos. Chem. Phys., 19, 12121–12140, https://doi.org/10.5194/acp-19-12121-2019, https://doi.org/10.5194/acp-19-12121-2019, 2019
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Shipborne measurements of nitryl chloride (ClNO2) were made during the AQABA (Air Quality and climate change in the Arabian BAsin) ship campaign in summer 2017. The dataset includes measurements over the Mediterranean Sea and around the Arabian Peninsula with observed mixing ratios ranging from the limit of detection to 600 pptv. We examined the regional variability in the generation of ClNO2 and its importance for Cl atom generation in a marine boundary layer influenced by ships and industry.
Duncan Watson-Parris, Nick Schutgens, Carly Reddington, Kirsty J. Pringle, Dantong Liu, James D. Allan, Hugh Coe, Ken S. Carslaw, and Philip Stier
Atmos. Chem. Phys., 19, 11765–11790, https://doi.org/10.5194/acp-19-11765-2019, https://doi.org/10.5194/acp-19-11765-2019, 2019
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The vertical distribution of aerosol in the atmosphere affects its ability to act as cloud condensation nuclei and changes the amount of sunlight it absorbs or reflects. Common global measurements of aerosol provide no information about this vertical distribution. Using a global collection of in situ aircraft measurements to compare with an aerosol–climate model (ECHAM-HAM), we explore the key processes controlling this distribution and find that wet removal plays a key role.
Michael Hollaway, Oliver Wild, Ting Yang, Yele Sun, Weiqi Xu, Conghui Xie, Lisa Whalley, Eloise Slater, Dwayne Heard, and Dantong Liu
Atmos. Chem. Phys., 19, 9699–9714, https://doi.org/10.5194/acp-19-9699-2019, https://doi.org/10.5194/acp-19-9699-2019, 2019
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This study, for the first time, uses combinations of aerosol and lidar data to drive an offline photolysis scheme. Absorbing species are shown to have the greatest impact on photolysis rate constants in the winter and scattering aerosol are shown to dominate responses in the summer. During haze episodes, aerosols are shown to produce a greater impact than cloud cover. The findings demonstrate the potential photochemical impacts of haze pollution in a highly polluted urban environment.
Fanny Peers, Peter Francis, Cathryn Fox, Steven J. Abel, Kate Szpek, Michael I. Cotterell, Nicholas W. Davies, Justin M. Langridge, Kerry G. Meyer, Steven E. Platnick, and Jim M. Haywood
Atmos. Chem. Phys., 19, 9595–9611, https://doi.org/10.5194/acp-19-9595-2019, https://doi.org/10.5194/acp-19-9595-2019, 2019
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The measurements from the geostationary satellite MSG/SEVIRI are used to retrieve the cloud and above-cloud aerosol properties over the South Atlantic. The technique relies on the spectral contrast and the magnitude of the signal in the visible to shortwave infrared region as well as the atmospheric correction based on forecasted water vapour profiles. The sensitivity analysis and the stability of the retrieval over time show great potential of the high-temporal-resolution observations.
Carly L. Reddington, William T. Morgan, Eoghan Darbyshire, Joel Brito, Hugh Coe, Paulo Artaxo, Catherine E. Scott, John Marsham, and Dominick V. Spracklen
Atmos. Chem. Phys., 19, 9125–9152, https://doi.org/10.5194/acp-19-9125-2019, https://doi.org/10.5194/acp-19-9125-2019, 2019
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We use an aerosol model and observations to explore model representation of aerosol emissions from fires in the Amazon. We find that observed aerosol concentrations are captured by the model over deforestation fires in the western Amazon but underestimated over savanna fires in the Cerrado environment. The model underestimates observed aerosol optical depth (AOD) even when the observed aerosol vertical profile is reproduced. We suggest this may be due to uncertainties in the AOD calculation.
Laura J. Wilcox, Nick Dunstone, Anna Lewinschal, Massimo Bollasina, Annica M. L. Ekman, and Eleanor J. Highwood
Atmos. Chem. Phys., 19, 9081–9095, https://doi.org/10.5194/acp-19-9081-2019, https://doi.org/10.5194/acp-19-9081-2019, 2019
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Asian anthropogenic aerosol emissions have increased rapidly since 1980. In winter, this has resulted in warming over China and cooling over India. Using models of different levels of complexity, we show that Asian-aerosol-induced heating anomalies in the western and northern North Pacific establish a circulation pattern that causes cooling in North America and Europe. This connection makes these regions potentially sensitive to any reductions of Asian aerosol emissions in the near future.
Jonathan W. Taylor, Sophie L. Haslett, Keith Bower, Michael Flynn, Ian Crawford, James Dorsey, Tom Choularton, Paul J. Connolly, Valerian Hahn, Christiane Voigt, Daniel Sauer, Régis Dupuy, Joel Brito, Alfons Schwarzenboeck, Thierry Bourriane, Cyrielle Denjean, Phil Rosenberg, Cyrille Flamant, James D. Lee, Adam R. Vaughan, Peter G. Hill, Barbara Brooks, Valéry Catoire, Peter Knippertz, and Hugh Coe
Atmos. Chem. Phys., 19, 8503–8522, https://doi.org/10.5194/acp-19-8503-2019, https://doi.org/10.5194/acp-19-8503-2019, 2019
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Low-level clouds cover a wide area of southern West Africa (SWA) and play an important role in the region's climate, reflecting sunlight away from the surface. We performed aircraft measurements of aerosols and clouds over SWA during the 2016 summer monsoon and found pollution, and polluted clouds, across the whole region. Smoke from biomass burning in Central Africa is transported to West Africa, causing a polluted background which limits the effect of local pollution on cloud properties.
Jamie M. Kelly, Ruth M. Doherty, Fiona M. O'Connor, Graham W. Mann, Hugh Coe, and Dantong Liu
Geosci. Model Dev., 12, 2539–2569, https://doi.org/10.5194/gmd-12-2539-2019, https://doi.org/10.5194/gmd-12-2539-2019, 2019
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This study develops the representation of secondary organic aerosol (SOA) within a global chemistry–climate model (UKCA). Both dry and wet deposition within the UKCA model are extended to consider precursors of SOA. The oxidation mechanism describing SOA formation is also extended by adding a reaction intermediate, with SOA yields that are dependent on oxidant concentrations.
Nicholas W. Davies, Cathryn Fox, Kate Szpek, Michael I. Cotterell, Jonathan W. Taylor, James D. Allan, Paul I. Williams, Jamie Trembath, Jim M. Haywood, and Justin M. Langridge
Atmos. Meas. Tech., 12, 3417–3434, https://doi.org/10.5194/amt-12-3417-2019, https://doi.org/10.5194/amt-12-3417-2019, 2019
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This research project assesses biases in traditional, filter-based, aerosol absorption measurements by comparison to state-of-the-art, non-filter-based, or in situ, measurements. We assess biases in traditional absorption measurements for three main aerosol types, including dust and fresh and aged biomass burning aerosols. The main results of this study are that the traditional and state-of-the-art absorption measurements are well correlated and that biases in the former are up to 45 %.
Sazzad Hossain, Hannah L. Cloke, Andrea Ficchì, Andrew G. Turner, and Elisabeth Stephens
Hydrol. Earth Syst. Sci. Discuss., https://doi.org/10.5194/hess-2019-286, https://doi.org/10.5194/hess-2019-286, 2019
Manuscript not accepted for further review
Weijun Li, Lei Liu, Qi Yuan, Liang Xu, Yanhong Zhu, Bingbing Wang, Hua Yu, Xiaokun Ding, Jian Zhang, Dao Huang, Dantong Liu, Wei Hu, Daizhou Zhang, Pingqing Fu, Maosheng Yao, Min Hu, Xiaoye Zhang, and Zongbo Shi
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2019-539, https://doi.org/10.5194/acp-2019-539, 2019
Preprint withdrawn
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The real state of individual primary biological aerosol particles (PBAPs) derived from natural sources is under mystery, although many studies well evaluate the morphology, mixing state, and elemental composition of anthropogenic particles. It induces that some studies mislead some anthropogenic particles into biological particles through electron microscopy. Here we firstly estimate the full database of individual PBAPs through two microscopic instruments. The database is good for research.
Zongbo Shi, Tuan Vu, Simone Kotthaus, Roy M. Harrison, Sue Grimmond, Siyao Yue, Tong Zhu, James Lee, Yiqun Han, Matthias Demuzere, Rachel E. Dunmore, Lujie Ren, Di Liu, Yuanlin Wang, Oliver Wild, James Allan, W. Joe Acton, Janet Barlow, Benjamin Barratt, David Beddows, William J. Bloss, Giulia Calzolai, David Carruthers, David C. Carslaw, Queenie Chan, Lia Chatzidiakou, Yang Chen, Leigh Crilley, Hugh Coe, Tie Dai, Ruth Doherty, Fengkui Duan, Pingqing Fu, Baozhu Ge, Maofa Ge, Daobo Guan, Jacqueline F. Hamilton, Kebin He, Mathew Heal, Dwayne Heard, C. Nicholas Hewitt, Michael Hollaway, Min Hu, Dongsheng Ji, Xujiang Jiang, Rod Jones, Markus Kalberer, Frank J. Kelly, Louisa Kramer, Ben Langford, Chun Lin, Alastair C. Lewis, Jie Li, Weijun Li, Huan Liu, Junfeng Liu, Miranda Loh, Keding Lu, Franco Lucarelli, Graham Mann, Gordon McFiggans, Mark R. Miller, Graham Mills, Paul Monk, Eiko Nemitz, Fionna O'Connor, Bin Ouyang, Paul I. Palmer, Carl Percival, Olalekan Popoola, Claire Reeves, Andrew R. Rickard, Longyi Shao, Guangyu Shi, Dominick Spracklen, David Stevenson, Yele Sun, Zhiwei Sun, Shu Tao, Shengrui Tong, Qingqing Wang, Wenhua Wang, Xinming Wang, Xuejun Wang, Zifang Wang, Lianfang Wei, Lisa Whalley, Xuefang Wu, Zhijun Wu, Pinhua Xie, Fumo Yang, Qiang Zhang, Yanli Zhang, Yuanhang Zhang, and Mei Zheng
Atmos. Chem. Phys., 19, 7519–7546, https://doi.org/10.5194/acp-19-7519-2019, https://doi.org/10.5194/acp-19-7519-2019, 2019
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APHH-Beijing is a collaborative international research programme to study the sources, processes and health effects of air pollution in Beijing. This introduction to the special issue provides an overview of (i) the APHH-Beijing programme, (ii) the measurement and modelling activities performed as part of it and (iii) the air quality and meteorological conditions during joint intensive field campaigns as a core activity within APHH-Beijing.
Dantong Liu, Rutambhara Joshi, Junfeng Wang, Chenjie Yu, James D. Allan, Hugh Coe, Michael J. Flynn, Conghui Xie, James Lee, Freya Squires, Simone Kotthaus, Sue Grimmond, Xinlei Ge, Yele Sun, and Pingqing Fu
Atmos. Chem. Phys., 19, 6749–6769, https://doi.org/10.5194/acp-19-6749-2019, https://doi.org/10.5194/acp-19-6749-2019, 2019
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This study provides source attribution and characterization of BC in the Beijing urban environment in both winter and summer. For the first time, the physically and chemically based source apportionments are compared to evaluate the primary source contribution and secondary processing of BC-containing particles. A method is proposed to isolate the BC from the transportation sector and coal combustion sources.
Eoghan Darbyshire, William T. Morgan, James D. Allan, Dantong Liu, Michael J. Flynn, James R. Dorsey, Sebastian J. O'Shea, Douglas Lowe, Kate Szpek, Franco Marenco, Ben T. Johnson, Stephane Bauguitte, Jim M. Haywood, Joel F. Brito, Paulo Artaxo, Karla M. Longo, and Hugh Coe
Atmos. Chem. Phys., 19, 5771–5790, https://doi.org/10.5194/acp-19-5771-2019, https://doi.org/10.5194/acp-19-5771-2019, 2019
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A novel analysis of aerosol and gas-phase vertical profiles shows a marked regional pollution contrast: composition is driven by the fire regime and vertical distribution is driven by thermodynamics. These drivers ought to be well represented in simulations to ensure realistic prediction of climate and air quality impacts. The BC : CO ratio in haze and plumes increases with altitude – long-range transport or fire stage coupled to plume dynamics may be responsible. Further enquiry is advocated.
James Brooks, James D. Allan, Paul I. Williams, Dantong Liu, Cathryn Fox, Jim Haywood, Justin M. Langridge, Ellie J. Highwood, Sobhan K. Kompalli, Debbie O'Sullivan, Suresh S. Babu, Sreedharan K. Satheesh, Andrew G. Turner, and Hugh Coe
Atmos. Chem. Phys., 19, 5615–5634, https://doi.org/10.5194/acp-19-5615-2019, https://doi.org/10.5194/acp-19-5615-2019, 2019
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Our study, for the first time, presents measurements of aerosol chemical composition and physical characteristics across northern India in the pre-monsoon and monsoon seasons of 2016 using the FAAM BAe-146 UK research aircraft. Across northern India, an elevated aerosol layer dominated by sulfate aerosol exists that diminishes with monsoon arrival. The Indo-Gangetic Plain (IGP) boundary layer is dominated by organics, whereas outside the IGP sulfate dominates with increased scattering aerosol.
Michael I. Cotterell, Andrew J. Orr-Ewing, Kate Szpek, Jim M. Haywood, and Justin M. Langridge
Atmos. Meas. Tech., 12, 2371–2385, https://doi.org/10.5194/amt-12-2371-2019, https://doi.org/10.5194/amt-12-2371-2019, 2019
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Photoacoustic spectroscopy provides measurements of absorption coefficient for aerosol and gas samples but requires careful calibration, and researchers often use concentrations of ozone. Recent work has shown that the bath gas composition impacts the accuracy of this calibration at visible wavelengths. We explore further the role of bath gas, demonstrating that the calibration accuracy is optimal for a bath gas composed of 20 % oxygen and 80 % nitrogen at wavelengths of 405, 514 and 658 nm.
Huang Zheng, Shaofei Kong, Fangqi Wu, Yi Cheng, Zhenzhen Niu, Shurui Zheng, Guowei Yang, Liquan Yao, Qin Yan, Jian Wu, Mingming Zheng, Nan Chen, Ke Xu, Yingying Yan, Dantong Liu, Delong Zhao, Tianliang Zhao, Yongqing Bai, Shuanglin Li, and Shihua Qi
Atmos. Chem. Phys., 19, 4499–4516, https://doi.org/10.5194/acp-19-4499-2019, https://doi.org/10.5194/acp-19-4499-2019, 2019
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This study simultaneously observed black carbon (BC) at five sites in central China and on the south edge of North China Plain, which have the most serious air pollution issues in China. The differences in BC properties between different air quality conditions and the property changes during transportation were studied. The main findings of this study were that during the downwind transportation of air, the BC mass concentration increased, whereas the absorption Ångström exponent decreased.
Thomas J. Bannan, Michael Le Breton, Michael Priestley, Stephen D. Worrall, Asan Bacak, Nicholas A. Marsden, Archit Mehra, Julia Hammes, Mattias Hallquist, M. Rami Alfarra, Ulrich K. Krieger, Jonathan P. Reid, John Jayne, Wade Robinson, Gordon McFiggans, Hugh Coe, Carl J. Percival, and Dave Topping
Atmos. Meas. Tech., 12, 1429–1439, https://doi.org/10.5194/amt-12-1429-2019, https://doi.org/10.5194/amt-12-1429-2019, 2019
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The Filter Inlet for Gases and AEROsols (FIGAERO) is an inlet designed to be coupled with a high-resolution time-of-flight chemical ionization mass spectrometer (HR-ToF-CIMS) and provides simultaneous molecular information relating to both the gas- and particle-phase samples. This method has been used to extract vapour pressures of compounds whilst giving quantitative concentrations in the particle phase. Here we detail an ideal set of benchmark compounds for characterization of the FIGAERO.
Nicholas A. Marsden, Romy Ullrich, Ottmar Möhler, Stine Eriksen Hammer, Konrad Kandler, Zhiqiang Cui, Paul I. Williams, Michael J. Flynn, Dantong Liu, James D. Allan, and Hugh Coe
Atmos. Chem. Phys., 19, 2259–2281, https://doi.org/10.5194/acp-19-2259-2019, https://doi.org/10.5194/acp-19-2259-2019, 2019
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The composition of airborne dust influences climate and ecosystems but its measurements presents a huge analytical challenge. Using online single-particle mass spectrometry, we demonstrate differences in mineralogy and mixing state can be detected in real time in both laboratory studies and ambient measurements. The results provide insights into the temporal and spatial evolution of dust properties that will be useful for aerosol–cloud interaction studies and dust cycle modelling.
Sophie L. Haslett, Jonathan W. Taylor, Konrad Deetz, Bernhard Vogel, Karmen Babić, Norbert Kalthoff, Andreas Wieser, Cheikh Dione, Fabienne Lohou, Joel Brito, Régis Dupuy, Alfons Schwarzenboeck, Paul Zieger, and Hugh Coe
Atmos. Chem. Phys., 19, 1505–1520, https://doi.org/10.5194/acp-19-1505-2019, https://doi.org/10.5194/acp-19-1505-2019, 2019
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As the population in West Africa grows and air pollution increases, it is becoming ever more important to understand the effects of this pollution on the climate and on health. Aerosol particles can grow by absorbing water from the air around them. This paper shows that during the monsoon season, aerosol particles in the region are likely to grow significantly because of the high moisture in the air. This means that climate effects from increasing pollution will be enhanced.
Junfeng Wang, Dantong Liu, Xinlei Ge, Yangzhou Wu, Fuzhen Shen, Mindong Chen, Jian Zhao, Conghui Xie, Qingqing Wang, Weiqi Xu, Jie Zhang, Jianlin Hu, James Allan, Rutambhara Joshi, Pingqing Fu, Hugh Coe, and Yele Sun
Atmos. Chem. Phys., 19, 447–458, https://doi.org/10.5194/acp-19-447-2019, https://doi.org/10.5194/acp-19-447-2019, 2019
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This work is part of the UK-China APHH campaign. We used a laser-only Aerodyne soot particle aerosol mass spectrometer, for the first time, to investigate the concentrations, size distributions and chemical compositions for those ambient submicron aerosol particles only with black carbon as cores. Our findings are valuable to understand the BC properties and processes in the densely populated megacities.
Conghui Xie, Weiqi Xu, Junfeng Wang, Qingqing Wang, Dantong Liu, Guiqian Tang, Ping Chen, Wei Du, Jian Zhao, Yingjie Zhang, Wei Zhou, Tingting Han, Qingyun Bian, Jie Li, Pingqing Fu, Zifa Wang, Xinlei Ge, James Allan, Hugh Coe, and Yele Sun
Atmos. Chem. Phys., 19, 165–179, https://doi.org/10.5194/acp-19-165-2019, https://doi.org/10.5194/acp-19-165-2019, 2019
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We present the first simultaneous real-time online measurements of aerosol optical properties at ground level and at 260 m on a meteorological tower in urban Beijing in winter. The vertical similarities and differences in scattering and absorption coefficients were characterized. The increases in MAC of BC were mainly associated with the coating materials on rBC. Coal combustion was the dominant source contribution of brown carbon followed by biomass burning and SOA in winter in Beijing.
Aditya Vaishya, Surendran Nair Suresh Babu, Venugopalan Jayachandran, Mukunda M. Gogoi, Naduparambil Bharathan Lakshmi, Krishnaswamy Krishna Moorthy, and Sreedharan Krishnakumari Satheesh
Atmos. Chem. Phys., 18, 17669–17685, https://doi.org/10.5194/acp-18-17669-2018, https://doi.org/10.5194/acp-18-17669-2018, 2018
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Aircraft-based measurements of vertical profiles of aerosol properties, across the Indo-Gangetic Plain (IGP), prior to onset of the Indian summer monsoon reveal a highly absorbing aerosol system over the IGP. Aerosols over the west IGP are mostly natural, larger in size and scatter light efficiently. Those over the central and eastern IGP are mostly anthropogenic in origin, smaller in size and absorb more light. Elevated absorbing aerosol layers may modulate regional precipitation patterns.
Claire L. Ryder, Franco Marenco, Jennifer K. Brooke, Victor Estelles, Richard Cotton, Paola Formenti, James B. McQuaid, Hannah C. Price, Dantong Liu, Patrick Ausset, Phil D. Rosenberg, Jonathan W. Taylor, Tom Choularton, Keith Bower, Hugh Coe, Martin Gallagher, Jonathan Crosier, Gary Lloyd, Eleanor J. Highwood, and Benjamin J. Murray
Atmos. Chem. Phys., 18, 17225–17257, https://doi.org/10.5194/acp-18-17225-2018, https://doi.org/10.5194/acp-18-17225-2018, 2018
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Every year, millions of tons of Saharan dust particles are carried across the Atlantic by the wind, where they can affect weather patterns and climate. Their sizes span orders of magnitude, but the largest (over 10 microns – around the width of a human hair) are difficult to measure and few observations exist. Here we show new aircraft observations of large dust particles, finding more than we would expect, and we quantify their properties which allow them to interact with atmospheric radiation.
D. S. Shaik, Y. Kant, D. Mitra, H. C. Chandola, and S. Suresh Babu
ISPRS Ann. Photogramm. Remote Sens. Spatial Inf. Sci., IV-5, 359–366, https://doi.org/10.5194/isprs-annals-IV-5-359-2018, https://doi.org/10.5194/isprs-annals-IV-5-359-2018, 2018
Christopher Dearden, Adrian Hill, Hugh Coe, and Tom Choularton
Atmos. Chem. Phys., 18, 14253–14269, https://doi.org/10.5194/acp-18-14253-2018, https://doi.org/10.5194/acp-18-14253-2018, 2018
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We perform computer simulations of the life cycle of low-lying clouds over southern West Africa during the monsoon season. Such clouds tend not to produce much precipitation, but they do affect the regional climate by modifying the amount of sunlight reaching the surface. The aim of this work is to understand the factors that influence the growth and break-up of these clouds. We show that the number of water droplets contained within the clouds affects how quickly they dissipate.
Konrad Deetz, Heike Vogel, Sophie Haslett, Peter Knippertz, Hugh Coe, and Bernhard Vogel
Atmos. Chem. Phys., 18, 14271–14295, https://doi.org/10.5194/acp-18-14271-2018, https://doi.org/10.5194/acp-18-14271-2018, 2018
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Water uptake can significantly increase the size and therefore alters the optical properties of aerosols. Our model study reveals that the high moisture and aerosol burden in the southern West African monsoon
layer makes it favorable to quantify properties that determine the aerosol liquid water content and its impact on the aerosol optical depth and radiative transfer. Especially in moist tropical environments the relative humidity impact on AOD has to be considered in atmospheric models.
Michael Priestley, Michael le Breton, Thomas J. Bannan, Stephen D. Worrall, Asan Bacak, Andrew R. D. Smedley, Ernesto Reyes-Villegas, Archit Mehra, James Allan, Ann R. Webb, Dudley E. Shallcross, Hugh Coe, and Carl J. Percival
Atmos. Chem. Phys., 18, 13481–13493, https://doi.org/10.5194/acp-18-13481-2018, https://doi.org/10.5194/acp-18-13481-2018, 2018
Wei Zhou, Jian Zhao, Bin Ouyang, Archit Mehra, Weiqi Xu, Yuying Wang, Thomas J. Bannan, Stephen D. Worrall, Michael Priestley, Asan Bacak, Qi Chen, Conghui Xie, Qingqing Wang, Junfeng Wang, Wei Du, Yingjie Zhang, Xinlei Ge, Penglin Ye, James D. Lee, Pingqing Fu, Zifa Wang, Douglas Worsnop, Roderic Jones, Carl J. Percival, Hugh Coe, and Yele Sun
Atmos. Chem. Phys., 18, 11581–11597, https://doi.org/10.5194/acp-18-11581-2018, https://doi.org/10.5194/acp-18-11581-2018, 2018
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We present measurements of gas-phase N2O5 and ClNO2 by ToF-CIMS during summer in urban Beijing as part of the APHH campaign. High reactivity of N2O5 indicative of active nocturnal chemistry was observed. The lifetime of N2O5 as a function of aerosol surface area and relative humidity was characterized, and N2O5 uptake coefficients were estimated. We also found that the N2O5 loss in this study is mainly attributed to its indirect loss via reactions of NO3 with VOCs and NO.
Jian Wu, Shaofei Kong, Fangqi Wu, Yi Cheng, Shurui Zheng, Qin Yan, Huang Zheng, Guowei Yang, Mingming Zheng, Dantong Liu, Delong Zhao, and Shihua Qi
Atmos. Chem. Phys., 18, 11623–11646, https://doi.org/10.5194/acp-18-11623-2018, https://doi.org/10.5194/acp-18-11623-2018, 2018
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In order to support regional modeling impact on air quality and policy making on controlling open biomass burning emissions, accurate open biomass burning emissions were estimated from 2003 to 2015 with high spatial and temporal resolution. Multiple satellite data, updated biomass data and survey results were all used to improve the accuracy. In addition, management policies and all influencing factors in rural areas for open biomass burning emissions were considered.
Claudia Christine Stephan, Nicholas P. Klingaman, Pier Luigi Vidale, Andrew G. Turner, Marie-Estelle Demory, and Liang Guo
Geosci. Model Dev., 11, 3215–3233, https://doi.org/10.5194/gmd-11-3215-2018, https://doi.org/10.5194/gmd-11-3215-2018, 2018
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Summer precipitation over China in the MetUM reaches twice its observed values. Increasing the horizontal resolution of the model and adding air–sea coupling have little effect on these biases. Nevertheless, MetUM correctly simulates spatial patterns of temporally coherent precipitation and the associated large-scale processes. This suggests that the model may provide useful predictions of summer intraseasonal variability despite the substantial biases in overall intraseasonal variance.
Kelly L. Pereira, Rachel Dunmore, James Whitehead, M. Rami Alfarra, James D. Allan, Mohammed S. Alam, Roy M. Harrison, Gordon McFiggans, and Jacqueline F. Hamilton
Atmos. Chem. Phys., 18, 11073–11096, https://doi.org/10.5194/acp-18-11073-2018, https://doi.org/10.5194/acp-18-11073-2018, 2018
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Exhaust emissions from a light-duty diesel engine were introduced into an atmospheric simulation chamber which was used as a holding-cell for sampling, allowing instruments capable of providing detailed chemical speciation of exhaust gas emissions to be used. The effect of different engine conditions on the exhaust gas composition was investigated. The exhaust composition changed considerably due to two influencing factors, engine combustion and diesel oxidative catalyst efficiency.
Konrad Deetz, Heike Vogel, Peter Knippertz, Bianca Adler, Jonathan Taylor, Hugh Coe, Keith Bower, Sophie Haslett, Michael Flynn, James Dorsey, Ian Crawford, Christoph Kottmeier, and Bernhard Vogel
Atmos. Chem. Phys., 18, 9767–9788, https://doi.org/10.5194/acp-18-9767-2018, https://doi.org/10.5194/acp-18-9767-2018, 2018
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Highly resolved process study simulations for 2–3 July are conducted with COSMO-ART to assess the aerosol direct and indirect effect on meteorological conditions over southern West Africa. The meteorological phenomena of Atlantic inflow and stratus-to-cumulus transition are identified as highly susceptible to the aerosol direct effect, leading to a spatial shift of the Atlantic inflow front and a temporal shift of the stratus-to-cumulus transition with changes in the aerosol amount.
Alexander J. Roberts, Margaret J. Woodage, John H. Marsham, Ellie J. Highwood, Claire L. Ryder, Willie McGinty, Simon Wilson, and Julia Crook
Atmos. Chem. Phys., 18, 9025–9048, https://doi.org/10.5194/acp-18-9025-2018, https://doi.org/10.5194/acp-18-9025-2018, 2018
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The summer Saharan dust hotspot is seasonally tied to the occurrence of convective storms. Global weather and climate models parameterise convection and so are unable to represent their associated dust uplift (haboobs). However, this work shows that even when simulations represent convection explicitly: (1) dust fields are not strongly affected, (2) convective storms are too small, (3) haboobs are too weak and (4) the land surface (bare soil and soil moisture) is dominant in controlling dust.
Sekou Keita, Cathy Liousse, Véronique Yoboué, Pamela Dominutti, Benjamin Guinot, Eric-Michel Assamoi, Agnès Borbon, Sophie L. Haslett, Laetitia Bouvier, Aurélie Colomb, Hugh Coe, Aristide Akpo, Jacques Adon, Julien Bahino, Madina Doumbia, Julien Djossou, Corinne Galy-Lacaux, Eric Gardrat, Sylvain Gnamien, Jean F. Léon, Money Ossohou, E. Touré N'Datchoh, and Laurent Roblou
Atmos. Chem. Phys., 18, 7691–7708, https://doi.org/10.5194/acp-18-7691-2018, https://doi.org/10.5194/acp-18-7691-2018, 2018
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This study provides emission factor (EF) data for elemental and organic carbon, total particulate matter and 58 volatile organic compound species for combustion sources specific to Africa to establish emission inventories with less uncertainty. EFs obtained in this study are generally higher than those in the literature whose values are used in emissions inventories for Africa. This shows that particles and VOC emissions were sometimes underestimated and underlines this study's importance.
Mingming Zheng, Shaofei Kong, Jianguo Bao, Ke Xu, Shurui Zheng, Guowei Yang, Jihong Quan, Lianxin Yuan, Nan Chen, Yiping Tian, Huang Zheng, Jian Wu, Dantong Liu, Delong Zhao, Qin Yan, Tianliang Zhao, and Shihua Qi
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2018-367, https://doi.org/10.5194/acp-2018-367, 2018
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In this paper, we study the aerosol acidity for different time scales, pollution episodes and air mass directions in a megacity of central China with high ambient temperature and relative humidity, and the impacting factors of pH were identified. This research is the first study concerning the aerosol acidity based on one-year online monitoring dataset with high resolution in central China, which is an important supplementary for the current aerosol acidity study around the world.
Claudia Christine Stephan, Nicholas P. Klingaman, Pier Luigi Vidale, Andrew G. Turner, Marie-Estelle Demory, and Liang Guo
Geosci. Model Dev., 11, 1823–1847, https://doi.org/10.5194/gmd-11-1823-2018, https://doi.org/10.5194/gmd-11-1823-2018, 2018
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Climate simulations are evaluated for their ability to reproduce year-to-year variability of precipitation over China. Mean precipitation and variability are too high in all simulations but improve with finer resolution and coupling. Simulations reproduce the observed spatial patterns of rainfall variability. However, not all of these patterns are associated with observed mechanisms. For example, simulations do not reproduce summer rainfall along the Yangtze valley in response to El Niño.
Amy K. Hodgson, William T. Morgan, Sebastian O'Shea, Stéphane Bauguitte, James D. Allan, Eoghan Darbyshire, Michael J. Flynn, Dantong Liu, James Lee, Ben Johnson, Jim M. Haywood, Karla M. Longo, Paulo E. Artaxo, and Hugh Coe
Atmos. Chem. Phys., 18, 5619–5638, https://doi.org/10.5194/acp-18-5619-2018, https://doi.org/10.5194/acp-18-5619-2018, 2018
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We flew a large atmospheric research aircraft across a number of different biomass burning environments in the Amazon Basin in September and October 2012. In this paper, we focus on smoke sampled very close to fresh fires (only 600–900 m above the fires and smoke that was 4–6 min old) to examine the chemical components that make up the smoke and their abundance. We found substantial differences in the emitted smoke that are due to the fuel type and combustion processes driving the fires.
Gillian D. Thornhill, Claire L. Ryder, Eleanor J. Highwood, Len C. Shaffrey, and Ben T. Johnson
Atmos. Chem. Phys., 18, 5321–5342, https://doi.org/10.5194/acp-18-5321-2018, https://doi.org/10.5194/acp-18-5321-2018, 2018
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We investigated the impact on the regional climate of different amounts of smoke emission (aerosol) from the burning of vegetation in South America using a climate model. We looked at differences between high and low smoke emissions and found impacts from the higher smoke emissions on the amount of cloud cover, solar radiation reaching the surface, wind patterns and rainfall. This means the local climate may be affected if there is more deforestation and more smoke from burning of vegetation.
Huang Zheng, Shaofei Kong, Xinli Xing, Yao Mao, Tianpeng Hu, Yang Ding, Gang Li, Dantong Liu, Shuanglin Li, and Shihua Qi
Atmos. Chem. Phys., 18, 4567–4595, https://doi.org/10.5194/acp-18-4567-2018, https://doi.org/10.5194/acp-18-4567-2018, 2018
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This research is the first study concerning the 1-year online monitoring of volatile organic compounds in an oil–gas field in China. The VOC concentrations, compositions and ozone formation potential in this study are quite different from other research. The contributions of natural gas and the other four sources to total VOCs are quantified. The different timescale variations in different sources are described. This research broadens our knowledge of VOC behavior in this type of region.
Riinu Ots, Mathew R. Heal, Dominique E. Young, Leah R. Williams, James D. Allan, Eiko Nemitz, Chiara Di Marco, Anais Detournay, Lu Xu, Nga L. Ng, Hugh Coe, Scott C. Herndon, Ian A. Mackenzie, David C. Green, Jeroen J. P. Kuenen, Stefan Reis, and Massimo Vieno
Atmos. Chem. Phys., 18, 4497–4518, https://doi.org/10.5194/acp-18-4497-2018, https://doi.org/10.5194/acp-18-4497-2018, 2018
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The main hypothesis of this paper is that people who live in large cities in the UK disobey the
smoke control lawas it has not been actively enforced for decades now. However, the use of wood in residential heating has increased, partly due to renewable energy targets, but also for discretionary (i.e. pleasant fireplaces) reasons. Our study is based mainly in London, but similar struggles with urban air quality due to residential wood and coal burning are seen in other major European cities.
James D. Lee, Stephen D. Mobbs, Axel Wellpott, Grant Allen, Stephane J.-B. Bauguitte, Ralph R. Burton, Richard Camilli, Hugh Coe, Rebecca E. Fisher, James L. France, Martin Gallagher, James R. Hopkins, Mathias Lanoiselle, Alastair C. Lewis, David Lowry, Euan G. Nisbet, Ruth M. Purvis, Sebastian O'Shea, John A. Pyle, and Thomas B. Ryerson
Atmos. Meas. Tech., 11, 1725–1739, https://doi.org/10.5194/amt-11-1725-2018, https://doi.org/10.5194/amt-11-1725-2018, 2018
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This work describes measurements, made from an aircraft platform, of the emission of methane and other organic gases from an uncontrolled leak from an oil platform in the North Sea (Total Elgin). The measurements made helped the platform operators to devise a strategy for repairing the leak and serve as a methodology for assessing future similar incidents.
Ernesto Reyes-Villegas, Michael Priestley, Yu-Chieh Ting, Sophie Haslett, Thomas Bannan, Michael Le Breton, Paul I. Williams, Asan Bacak, Michael J. Flynn, Hugh Coe, Carl Percival, and James D. Allan
Atmos. Chem. Phys., 18, 4093–4111, https://doi.org/10.5194/acp-18-4093-2018, https://doi.org/10.5194/acp-18-4093-2018, 2018
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This work presents the analysis of a special event with high biomass burning emissions, named Bonfire Night. Nitrogen chemistry was observed and it was possible to study the night time chemistry. It was possible to quantify particulate organic oxides of nitrogen (PON) concentrations of 2.8 µg m−3 using 46 : 30 ratios from aerosol mass spectrometry measurements. The use of the receptor model positive matrix factorization (PMF) allowed to separate organic aerosols into different sources.
Dantong Liu, Jonathan W. Taylor, Jonathan Crosier, Nicholas Marsden, Keith N. Bower, Gary Lloyd, Claire L. Ryder, Jennifer K. Brooke, Richard Cotton, Franco Marenco, Alan Blyth, Zhiqiang Cui, Victor Estelles, Martin Gallagher, Hugh Coe, and Tom W. Choularton
Atmos. Chem. Phys., 18, 3817–3838, https://doi.org/10.5194/acp-18-3817-2018, https://doi.org/10.5194/acp-18-3817-2018, 2018
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This article presents measurements of aerosol properties off the coast of west Africa during August 2015. For the first time, an airborne laser-induced incandescence instrument was deployed to measure the hematite content of dust. The single scattering albedo of dust was found to be influenced by the hematite content, but depended on the dust source and potential dust age. This highlights the importance of size-dependent composition in determining the optical properties of dust.
Lisa K. Whalley, Daniel Stone, Rachel Dunmore, Jacqueline Hamilton, James R. Hopkins, James D. Lee, Alastair C. Lewis, Paul Williams, Jörg Kleffmann, Sebastian Laufs, Robert Woodward-Massey, and Dwayne E. Heard
Atmos. Chem. Phys., 18, 2547–2571, https://doi.org/10.5194/acp-18-2547-2018, https://doi.org/10.5194/acp-18-2547-2018, 2018
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This paper presents the first radical observations made in London and subsequent model comparisons. This work highlights that there are uncertainties in the degradation mechanism of complex biogenic and diesel-related VOC species under low-NOx conditions and under high-NOx conditions there is a missing source of RO2 radicals. The impact of these model uncertainties on in situ ozone production as a function of NOx is discussed.
Joel Brito, Evelyn Freney, Pamela Dominutti, Agnes Borbon, Sophie L. Haslett, Anneke M. Batenburg, Aurelie Colomb, Regis Dupuy, Cyrielle Denjean, Frederic Burnet, Thierry Bourriane, Adrien Deroubaix, Karine Sellegri, Stephan Borrmann, Hugh Coe, Cyrille Flamant, Peter Knippertz, and Alfons Schwarzenboeck
Atmos. Chem. Phys., 18, 757–772, https://doi.org/10.5194/acp-18-757-2018, https://doi.org/10.5194/acp-18-757-2018, 2018
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This work focuses on sources of submicron aerosol particles over southern West Africa (SWA). Results have shown that isoprene, a gas-phase compound of biogenic origin, is responsible for roughly 25 % of the organic aerosol (OA) loading, under most background or urban plumes alike. This fraction represents a lower estimate from the biogenic contribution in this fairly polluted region. This work sheds light upon the role of anthropogenic and biogenic emissions on the pollution burden over SWA.
Sophie L. Haslett, J. Chris Thomas, William T. Morgan, Rory Hadden, Dantong Liu, James D. Allan, Paul I. Williams, Sekou Keita, Cathy Liousse, and Hugh Coe
Atmos. Chem. Phys., 18, 385–403, https://doi.org/10.5194/acp-18-385-2018, https://doi.org/10.5194/acp-18-385-2018, 2018
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Wood burning is chaotic, so the particles emitted can be difficult to study in a repeatable way. Here, we addressed this problem by carefully controlling small wood fires in the lab. We saw three burning phases, which could be told apart chemically; we also saw evidence of these in measurements of wood burning in London in 2012. Controlled experiments like this help us to understand why emissions are so variable and to recognise burning conditions just from the particles seen in the atmosphere.
Nicholas A. Marsden, Michael J. Flynn, James D. Allan, and Hugh Coe
Atmos. Meas. Tech., 11, 195–213, https://doi.org/10.5194/amt-11-195-2018, https://doi.org/10.5194/amt-11-195-2018, 2018
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Mineralogy of silicate mineral dust has a strong influence on climate and ecosystems due to variation in physiochemical properties that result from differences in composition and crystal structure (mineral phase). Traditional offline methods of analysing mineral phase are labour intensive and the temporal resolution of the data is lost. We introduce a novel technique that enables the online differentiation of mineral phase in silicate particles by single-particle mass spectrometry.
Delong Zhao, Mengyu Huang, Dantong Liu, Deping Ding, Ping Tian, Quan Liu, Wei Zhou, Jiujiang Sheng, Fei Wang, Kai Bi, Yan Yang, Xia Li, Yaqiong Hu, Xin Guo, Yang Gao, Hui He, Yunbo Chen, Shaofei Kong, and Jiayi Huang
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2017-1118, https://doi.org/10.5194/acp-2017-1118, 2018
Preprint withdrawn
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This study for the first time reports the 3D distributions of black carbon and detailed physical properties in the boundary layer over the North China Plain, using intensive aircraft measurements in both hot and cold seasons. The BC mass in the planetary boundary layer (PBL) was found to be largely influenced by meteorology which modulated the local emission and regional transport.
Sebastian J. O'Shea, Thomas W. Choularton, Michael Flynn, Keith N. Bower, Martin Gallagher, Jonathan Crosier, Paul Williams, Ian Crawford, Zoë L. Fleming, Constantino Listowski, Amélie Kirchgaessner, Russell S. Ladkin, and Thomas Lachlan-Cope
Atmos. Chem. Phys., 17, 13049–13070, https://doi.org/10.5194/acp-17-13049-2017, https://doi.org/10.5194/acp-17-13049-2017, 2017
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Few direct measurements have been made of Antarctic cloud and aerosol properties. As part of the 2015 Microphysics of Antarctic Clouds (MAC) field campaign, detailed airborne and ground-based measurements were made over the Weddell Sea and Antarctic coastal continent. This paper presents the first results from this campaign and discusses the cloud properties and processes important in this region.
Gaurav Govardhan, Sreedharan Krishnakumari Satheesh, Ravi Nanjundiah, Krishnaswamy Krishna Moorthy, and Surendran Suresh Babu
Atmos. Chem. Phys., 17, 9623–9644, https://doi.org/10.5194/acp-17-9623-2017, https://doi.org/10.5194/acp-17-9623-2017, 2017
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Using a model, we show that black carbon emissions from aircraft are most likely responsible for the observed high-altitude BC layers over the Indian region. Our analysis of model simulations and CALIPSO data shows that such aircraft-emitted BC layers can be vertically transported into the UTLS region upon their interaction with the underlying strong monsoonal convection. Such lifted BC layers, which intrude into the stratosphere, can potentially harm the stratospheric ozone layer.
David O. Topping, James Allan, M. Rami Alfarra, and Bernard Aumont
Geosci. Model Dev., 10, 2365–2377, https://doi.org/10.5194/gmd-10-2365-2017, https://doi.org/10.5194/gmd-10-2365-2017, 2017
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Our ability to model the chemical and thermodynamic processes that lead to secondary organic aerosol (SOA) formation is thought to be hampered by the complexity of the system. In this proof of concept study, the ability to train supervised methods to predict electron impact ionisation (EI) mass spectra for the AMS is evaluated to facilitate improved model evaluation. The study demonstrates the use of a methodology that would be improved with more training data and data from simple mixed systems.
Alexandra Tsekeri, Vassilis Amiridis, Franco Marenco, Athanasios Nenes, Eleni Marinou, Stavros Solomos, Phil Rosenberg, Jamie Trembath, Graeme J. Nott, James Allan, Michael Le Breton, Asan Bacak, Hugh Coe, Carl Percival, and Nikolaos Mihalopoulos
Atmos. Meas. Tech., 10, 83–107, https://doi.org/10.5194/amt-10-83-2017, https://doi.org/10.5194/amt-10-83-2017, 2017
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The In situ/Remote sensing aerosol Retrieval Algorithm (IRRA) provides vertical profiles of aerosol optical, microphysical and hygroscopic properties from airborne in situ and remote sensing measurements. The algorithm is highly advantageous for aerosol characterization in humid conditions, employing the ISORROPIA II model for acquiring the particle hygroscopic growth. IRRA can find valuable applications in aerosol–cloud interaction schemes and in validation of active space-borne sensors.
Ernesto Reyes-Villegas, David C. Green, Max Priestman, Francesco Canonaco, Hugh Coe, André S. H. Prévôt, and James D. Allan
Atmos. Chem. Phys., 16, 15545–15559, https://doi.org/10.5194/acp-16-15545-2016, https://doi.org/10.5194/acp-16-15545-2016, 2016
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For the first time in the UK, an Aerosol Chemical Speciation Monitor was used to measure aerosol concentrations in London in March–December 2013, with further organic aerosol (OA) source apportionment using the ME-2 factorization tool. Five OA sources were identified: biomass burning OA, hydrocarbon-like OA, cooking OA, semivolatile oxygenated OA and low-volatility oxygenated OA. This information can be used to take future action on the respective legislation in order to improve the air quality.
Nicholas Marsden, Michael J. Flynn, Jonathan W. Taylor, James D. Allan, and Hugh Coe
Atmos. Meas. Tech., 9, 6051–6068, https://doi.org/10.5194/amt-9-6051-2016, https://doi.org/10.5194/amt-9-6051-2016, 2016
Ben T. Johnson, James M. Haywood, Justin M. Langridge, Eoghan Darbyshire, William T. Morgan, Kate Szpek, Jennifer K. Brooke, Franco Marenco, Hugh Coe, Paulo Artaxo, Karla M. Longo, Jane P. Mulcahy, Graham W. Mann, Mohit Dalvi, and Nicolas Bellouin
Atmos. Chem. Phys., 16, 14657–14685, https://doi.org/10.5194/acp-16-14657-2016, https://doi.org/10.5194/acp-16-14657-2016, 2016
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Biomass burning is a large source of carbonaceous aerosols, which scatter and absorb solar radiation, and modify cloud properties. We evaluate the simulation of biomass burning aerosol processes and properties in the HadGEM3 climate model using observations, including those from the South American Biomass Burning Analysis. We find that modelled aerosol optical depths are underestimated unless aerosol emissions (Global Fire Emission Database v3) are increased by a factor of 1.6–2.0.
Gillian Young, Hazel M. Jones, Thomas W. Choularton, Jonathan Crosier, Keith N. Bower, Martin W. Gallagher, Rhiannon S. Davies, Ian A. Renfrew, Andrew D. Elvidge, Eoghan Darbyshire, Franco Marenco, Philip R. A. Brown, Hugo M. A. Ricketts, Paul J. Connolly, Gary Lloyd, Paul I. Williams, James D. Allan, Jonathan W. Taylor, Dantong Liu, and Michael J. Flynn
Atmos. Chem. Phys., 16, 13945–13967, https://doi.org/10.5194/acp-16-13945-2016, https://doi.org/10.5194/acp-16-13945-2016, 2016
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Clouds are intricately coupled to the Arctic sea ice. Our inability to accurately model cloud fractions causes large uncertainties in predicted radiative interactions in this region, therefore, affecting sea ice forecasts. Here, we present measurements of cloud microphysics, aerosol properties, and thermodynamic structure over the transition from sea ice to ocean to improve our understanding of the relationship between the Arctic atmosphere and clouds which develop in this region.
Riinu Ots, Massimo Vieno, James D. Allan, Stefan Reis, Eiko Nemitz, Dominique E. Young, Hugh Coe, Chiara Di Marco, Anais Detournay, Ian A. Mackenzie, David C. Green, and Mathew R. Heal
Atmos. Chem. Phys., 16, 13773–13789, https://doi.org/10.5194/acp-16-13773-2016, https://doi.org/10.5194/acp-16-13773-2016, 2016
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Emissions of cooking organic aerosol (COA; from charbroiling, frying, etc.) are currently absent in European emissions inventories yet measurements have pointed to significant COA concentrations. In this study, emissions of COA were developed for the UK by model iteration against year-long measurements at two sites in London. Modelled COA dropped rapidly outside of major urban areas, suggesting that although a notable component in UK urban air, COA does not have a significant effect on rural PM.
Tianjun Zhou, Andrew G. Turner, James L. Kinter, Bin Wang, Yun Qian, Xiaolong Chen, Bo Wu, Bin Wang, Bo Liu, Liwei Zou, and Bian He
Geosci. Model Dev., 9, 3589–3604, https://doi.org/10.5194/gmd-9-3589-2016, https://doi.org/10.5194/gmd-9-3589-2016, 2016
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This paper tells why to launch the Global Monsoons Model Inter-comparison Project (GMMIP) and how to achieve its scientific goals on monsoon variability. It addresses the scientific questions to be answered, describes three tiered experiments comprehensively and proposes a basic analysis framework to guide future research. It will help the monsoon research communities to understand the objectives of the GMMIP and the modelling groups involved in the GMMIP conduct the experiments successfully.
Jonathan W. Taylor, Thomas W. Choularton, Alan M. Blyth, Michael J. Flynn, Paul I. Williams, Gillian Young, Keith N. Bower, Jonathan Crosier, Martin W. Gallagher, James R. Dorsey, Zixia Liu, and Philip D. Rosenberg
Atmos. Chem. Phys., 16, 11687–11709, https://doi.org/10.5194/acp-16-11687-2016, https://doi.org/10.5194/acp-16-11687-2016, 2016
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We present measurements of boundary layer aerosol concentration, size and composition from research flights performed over the southwest peninsula of the UK during the COnvective Precipitation Experiment (COPE) of summer 2013. We compare case studies of aerosol in cleaner marine air from the Atlantic with anthropogenic pollution from the UK. These measurements are then used to investigate the possible sources of CCN and IN in the region.
James D. Whitehead, Eoghan Darbyshire, Joel Brito, Henrique M. J. Barbosa, Ian Crawford, Rafael Stern, Martin W. Gallagher, Paul H. Kaye, James D. Allan, Hugh Coe, Paulo Artaxo, and Gordon McFiggans
Atmos. Chem. Phys., 16, 9727–9743, https://doi.org/10.5194/acp-16-9727-2016, https://doi.org/10.5194/acp-16-9727-2016, 2016
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We present measurements of aerosols during the transition from wet to dry seasons at a pristine rainforest site in central Amazonia. By excluding pollution episodes, we focus on natural biogenic aerosols. Submicron aerosols are dominated by organic material, similar to previous wet season measurements. Larger particles are dominated by biological material, mostly fungal spores, with higher concentrations at night. This study provides important data on the nature of particles above the Amazon.
Anna R. Esteve, Eleanor J. Highwood, and Claire L. Ryder
Atmos. Chem. Phys., 16, 7639–7651, https://doi.org/10.5194/acp-16-7639-2016, https://doi.org/10.5194/acp-16-7639-2016, 2016
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The radiative effect of aerosols over Europe during the EUCAARI-LONGREX campaign has been calculated using measurements made by the FAAM BAe-146 aircraft and radiative transfer modelling. For one specially designed flight, simulated irradiances have been compared to radiation measurements to explore the validity of model assumptions. We have quantified the uncertainties in our calculations due to the way in which aerosols and other parameters are represented in a radiative transfer model.
Riinu Ots, Dominique E. Young, Massimo Vieno, Lu Xu, Rachel E. Dunmore, James D. Allan, Hugh Coe, Leah R. Williams, Scott C. Herndon, Nga L. Ng, Jacqueline F. Hamilton, Robert Bergström, Chiara Di Marco, Eiko Nemitz, Ian A. Mackenzie, Jeroen J. P. Kuenen, David C. Green, Stefan Reis, and Mathew R. Heal
Atmos. Chem. Phys., 16, 6453–6473, https://doi.org/10.5194/acp-16-6453-2016, https://doi.org/10.5194/acp-16-6453-2016, 2016
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This study investigates the contribution of diesel vehicle emissions to organic aerosol formation and particulate matter concentrations in London. Comparisons of simulated pollutant concentrations with observations show good agreement and give confidence in the skill of the model applied. The contribution of diesel vehicle emissions, which are currently not included in official emissions inventories, is demonstrated to be substantial, indicating that more research on this topic is required.
J. D. Lee, L. K. Whalley, D. E. Heard, D. Stone, R. E. Dunmore, J. F. Hamilton, D. E. Young, J. D. Allan, S. Laufs, and J. Kleffmann
Atmos. Chem. Phys., 16, 2747–2764, https://doi.org/10.5194/acp-16-2747-2016, https://doi.org/10.5194/acp-16-2747-2016, 2016
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This paper presents field measurements of HONO and a range of other gas phase and particulate species from an urban background site in London. The measured daytime HONO cannot be reproduced with a simple box model and thus a significant daytime missing source of HONO is present. We show that this missing source could be responsible for 40 % of the OH radical source and 57 % of the OH initiation; hence its potential importance for atmospheric oxidation and ozone production.
Anthony C. Jones, James M. Haywood, and Andy Jones
Atmos. Chem. Phys., 16, 2843–2862, https://doi.org/10.5194/acp-16-2843-2016, https://doi.org/10.5194/acp-16-2843-2016, 2016
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In this paper we assess the potential climatic impacts of geoengineering with sulfate, black carbon and titania injection strategies. We find that black carbon injection results in severe stratospheric warming and precipitation impacts, and therefore black carbon is unsuitable for geoengineering purposes. As the injection rates and climatic impacts for titania are close to those for sulfate, there appears little benefit of using titania when compared to injection of sulfur dioxide.
L. Xu, L. R. Williams, D. E. Young, J. D. Allan, H. Coe, P. Massoli, E. Fortner, P. Chhabra, S. Herndon, W. A. Brooks, J. T. Jayne, D. R. Worsnop, A. C. Aiken, S. Liu, K. Gorkowski, M. K. Dubey, Z. L. Fleming, S. Visser, A. S. H. Prévôt, and N. L. Ng
Atmos. Chem. Phys., 16, 1139–1160, https://doi.org/10.5194/acp-16-1139-2016, https://doi.org/10.5194/acp-16-1139-2016, 2016
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We investigate the spatial distribution of submicron aerosol in the greater London area as part of the Clean Air for London (ClearfLo) project in winter 2012. Although the concentrations of organic aerosol (OA) are similar between a rural and an urban site, the OA sources are different. We also examine the volatility of submicron aerosol at the rural site and find that the non-volatile organics have similar sources or have undergone similar chemical processing as refractory black carbon.
J. W. Taylor, T. W. Choularton, A. M. Blyth, Z. Liu, K. N. Bower, J. Crosier, M. W. Gallagher, P. I. Williams, J. R. Dorsey, M. J. Flynn, L. J. Bennett, Y. Huang, J. French, A. Korolev, and P. R. A. Brown
Atmos. Chem. Phys., 16, 799–826, https://doi.org/10.5194/acp-16-799-2016, https://doi.org/10.5194/acp-16-799-2016, 2016
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We present microphysical observations of cumulus clouds measured over south-west England during COPE in summer 2013. Detailed sampling focused on an isolated liquid cloud that glaciated as it matured to merge with a band of cloud downwind. The first ice particles observed were frozen drizzle, while columnar ice dominated in the mature stages. We discuss the interactions between the warm rain and secondary ice processes, and their importance for the formation of precipitation.
J. C. Corbin, A. Othman, J. D. Allan, D. R. Worsnop, J. D. Haskins, B. Sierau, U. Lohmann, and A. A. Mensah
Atmos. Meas. Tech., 8, 4615–4636, https://doi.org/10.5194/amt-8-4615-2015, https://doi.org/10.5194/amt-8-4615-2015, 2015
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Peak-integration uncertainties in the Aerodyne high-resolution aerosol mass spectrometer (AMS) are analyzed in detail using a combination of empirical data analysis and Monte Carlo approaches. The most general conclusion, applicable to any mass spectrometer, is that non-zero mass accuracy leads to a percentage error in constrained peak fits, even for well-resolved peaks. For overlapping peaks, this mass-accuracy effect may be viewed as a reduction in the effective m/z-calibration precision.
W. W. Hu, P. Campuzano-Jost, B. B. Palm, D. A. Day, A. M. Ortega, P. L. Hayes, J. E. Krechmer, Q. Chen, M. Kuwata, Y. J. Liu, S. S. de Sá, K. McKinney, S. T. Martin, M. Hu, S. H. Budisulistiorini, M. Riva, J. D. Surratt, J. M. St. Clair, G. Isaacman-Van Wertz, L. D. Yee, A. H. Goldstein, S. Carbone, J. Brito, P. Artaxo, J. A. de Gouw, A. Koss, A. Wisthaler, T. Mikoviny, T. Karl, L. Kaser, W. Jud, A. Hansel, K. S. Docherty, M. L. Alexander, N. H. Robinson, H. Coe, J. D. Allan, M. R. Canagaratna, F. Paulot, and J. L. Jimenez
Atmos. Chem. Phys., 15, 11807–11833, https://doi.org/10.5194/acp-15-11807-2015, https://doi.org/10.5194/acp-15-11807-2015, 2015
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This work summarized all the studies reporting isoprene epoxydiols-derived secondary organic aerosol (IEPOX-SOA) measured globally by aerosol mass spectrometer and compare them with modeled gas-phase IEPOX, with results suggestive of the importance of IEPOX-SOA for regional and global OA budgets. A real-time tracer of IEPOX-SOA is thoroughly evaluated for the first time by combing multiple field and chamber studies. A quick and easy empirical method on IEPOX-SOA estimation is also presented.
D. Liu, B. Quennehen, E. Darbyshire, J. D. Allan, P. I. Williams, J. W. Taylor, S. J.-B. Bauguitte, M. J. Flynn, D. Lowe, M. W. Gallagher, K. N. Bower, T. W. Choularton, and H. Coe
Atmos. Chem. Phys., 15, 11537–11555, https://doi.org/10.5194/acp-15-11537-2015, https://doi.org/10.5194/acp-15-11537-2015, 2015
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We show that during the springtime of 2013, the anthropogenic pollution particularly from sources in Asia, contributed significantly to black carbon across the European Arctic free troposphere. In contrast to previous studies, the contribution from open wildfires was minimal. Given that Asian pollution is likely to continue to rise over the coming years, it is likely that the radiative forcing in the Arctic will also continue to increase.
S. Visser, J. G. Slowik, M. Furger, P. Zotter, N. Bukowiecki, F. Canonaco, U. Flechsig, K. Appel, D. C. Green, A. H. Tremper, D. E. Young, P. I. Williams, J. D. Allan, H. Coe, L. R. Williams, C. Mohr, L. Xu, N. L. Ng, E. Nemitz, J. F. Barlow, C. H. Halios, Z. L. Fleming, U. Baltensperger, and A. S. H. Prévôt
Atmos. Chem. Phys., 15, 11291–11309, https://doi.org/10.5194/acp-15-11291-2015, https://doi.org/10.5194/acp-15-11291-2015, 2015
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Trace element measurements in three particle size ranges (PM10-2.5, PM2.5-1.0 and PM1.0-0.3) were performed with 2h time resolution at kerbside, urban background and rural sites during the ClearfLo winter 2012 campaign in London. The environment-dependent variability of emissions was characterized using the Multilinear Engine implementation of the positive matrix factorization model. A total of nine different factors were resolved from local, regional and natural origin.
C. L. Ryder, J. B. McQuaid, C. Flamant, P. D. Rosenberg, R. Washington, H. E. Brindley, E. J. Highwood, J. H. Marsham, D. J. Parker, M. C. Todd, J. R. Banks, J. K. Brooke, S. Engelstaedter, V. Estelles, P. Formenti, L. Garcia-Carreras, C. Kocha, F. Marenco, H. Sodemann, C. J. T. Allen, A. Bourdon, M. Bart, C. Cavazos-Guerra, S. Chevaillier, J. Crosier, E. Darbyshire, A. R. Dean, J. R. Dorsey, J. Kent, D. O'Sullivan, K. Schepanski, K. Szpek, J. Trembath, and A. Woolley
Atmos. Chem. Phys., 15, 8479–8520, https://doi.org/10.5194/acp-15-8479-2015, https://doi.org/10.5194/acp-15-8479-2015, 2015
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Measurements of the Saharan atmosphere and of atmospheric mineral dust are lacking but are vital to our understanding of the climate of this region and their impacts further afield. Novel observations were made by the Fennec climate programme during June 2011 and 2012 using ground-based, remote sensing and airborne platforms. Here we describe the airborne observations and the contributions they have made to furthering our understanding of the Saharan climate system.
E. Athanasopoulou, A. P. Protonotariou, E. Bossioli, A. Dandou, M. Tombrou, J. D. Allan, H. Coe, N. Mihalopoulos, J. Kalogiros, A. Bacak, J. Sciare, and G. Biskos
Atmos. Chem. Phys., 15, 8401–8421, https://doi.org/10.5194/acp-15-8401-2015, https://doi.org/10.5194/acp-15-8401-2015, 2015
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A model system is evaluated versus ground and airborne aerosol measurements, towards the identification of its competencies and deficiencies over the eastern Mediterranean (EM) during summer. Secondary organic aerosol (OA) formation is investigated towards improving OA behaviour. Biomass burning is a significant particle source, largely explaining OA underestimation (ca. 50%). More than 70% of the aerosol mass over the EM is related to trans-boundary transport during strong northeastern winds.
M. J. Alvarado, C. R. Lonsdale, R. J. Yokelson, S. K. Akagi, H. Coe, J. S. Craven, E. V. Fischer, G. R. McMeeking, J. H. Seinfeld, T. Soni, J. W. Taylor, D. R. Weise, and C. E. Wold
Atmos. Chem. Phys., 15, 6667–6688, https://doi.org/10.5194/acp-15-6667-2015, https://doi.org/10.5194/acp-15-6667-2015, 2015
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Being able to understand and simulate the chemical evolution of biomass burning smoke plumes under a wide variety of conditions is a critical part of forecasting the impact of these fires on air quality, atmospheric composition, and climate. Here we use an improved model of this chemistry to simulate the evolution of ozone and secondary organic aerosol within a young biomass burning smoke plume from the Williams prescribed burn in chaparral, which was sampled over California in November 2009.
D. E. Young, J. D. Allan, P. I. Williams, D. C. Green, M. J. Flynn, R. M. Harrison, J. Yin, M. W. Gallagher, and H. Coe
Atmos. Chem. Phys., 15, 6351–6366, https://doi.org/10.5194/acp-15-6351-2015, https://doi.org/10.5194/acp-15-6351-2015, 2015
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For the first time, the behaviour of non-refractory inorganic and organic submicron particulates through an entire annual cycle is investigated at a UK urban background site. We show secondary aerosols account for a significant fraction of the submicron aerosol burden, high concentration events are governed by different factors depending on season, and on an annual basis there is no variability in the extent of secondary organic aerosol oxidation.
L. Guo, A. G. Turner, and E. J. Highwood
Atmos. Chem. Phys., 15, 6367–6378, https://doi.org/10.5194/acp-15-6367-2015, https://doi.org/10.5194/acp-15-6367-2015, 2015
J. D. Allan, P. I. Williams, J. Najera, J. D. Whitehead, M. J. Flynn, J. W. Taylor, D. Liu, E. Darbyshire, L. J. Carpenter, R. Chance, S. J. Andrews, S. C. Hackenberg, and G. McFiggans
Atmos. Chem. Phys., 15, 5599–5609, https://doi.org/10.5194/acp-15-5599-2015, https://doi.org/10.5194/acp-15-5599-2015, 2015
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New particle formation (NPF) is an important contributor to aerosol number concentrations in the Arctic and thus has a major role in dictating cloud properties and climate in this region. Here we present direct evidence that the oxidation of iodine in the atmosphere causes NPF in the Greenland Sea. This is important because this is a NPF mechanism that has not previously been considered in modelling studies at these latitudes.
J. W. Taylor, J. D. Allan, D. Liu, M. Flynn, R. Weber, X. Zhang, B. L. Lefer, N. Grossberg, J. Flynn, and H. Coe
Atmos. Meas. Tech., 8, 1701–1718, https://doi.org/10.5194/amt-8-1701-2015, https://doi.org/10.5194/amt-8-1701-2015, 2015
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When using the SP2 to report black carbon core/shell coating thickness, the core density and refractive index must be estimated from literature values. We systematically vary the assumed parameters and the instrument calibration, and quantify the effects in the derived coatings. The technique is highly sensitive to the core refractive index but has only a minor sensitivity to the core density and coating refractive index. We identify the most appropriate values to use in future analysis.
Q. Chen, D. K. Farmer, L. V. Rizzo, T. Pauliquevis, M. Kuwata, T. G. Karl, A. Guenther, J. D. Allan, H. Coe, M. O. Andreae, U. Pöschl, J. L. Jimenez, P. Artaxo, and S. T. Martin
Atmos. Chem. Phys., 15, 3687–3701, https://doi.org/10.5194/acp-15-3687-2015, https://doi.org/10.5194/acp-15-3687-2015, 2015
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Submicron particle mass concentration in the Amazon during the wet season of 2008 was dominated by organic material. The PMF analysis finds a comparable importance of gas-phase (gas-to-particle condensation) and particle-phase (reactive uptake of isoprene oxidation products, especially of epoxydiols to acidic haze, fog, or cloud droplets) production of secondary organic material during the study period, together accounting for >70% of the organic-particle mass concentration.
L. R. Crilley, W. J. Bloss, J. Yin, D. C. S. Beddows, R. M. Harrison, J. D. Allan, D. E. Young, M. Flynn, P. Williams, P. Zotter, A. S. H. Prevot, M. R. Heal, J. F. Barlow, C. H. Halios, J. D. Lee, S. Szidat, and C. Mohr
Atmos. Chem. Phys., 15, 3149–3171, https://doi.org/10.5194/acp-15-3149-2015, https://doi.org/10.5194/acp-15-3149-2015, 2015
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Wood is a renewable fuel but its combustion for residential heating releases a number of locally acting air pollutants, most notably particulate matter known to have adverse effects on human health. This paper used chemical tracers for wood smoke to estimate the contribution that burning wood makes to concentrations of airborne particles in the atmosphere of southern England and most particularly in London.
M. D. Jolleys, H. Coe, G. McFiggans, J. W. Taylor, S. J. O'Shea, M. Le Breton, S. J.-B. Bauguitte, S. Moller, P. Di Carlo, E. Aruffo, P. I. Palmer, J. D. Lee, C. J. Percival, and M. W. Gallagher
Atmos. Chem. Phys., 15, 3077–3095, https://doi.org/10.5194/acp-15-3077-2015, https://doi.org/10.5194/acp-15-3077-2015, 2015
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Particulate emissions in the form of organic aerosol from boreal forest fires in Canada have been measured during an aircraft measurement campaign. Ratios of the amount of aerosol emitted relative to gas species such as CO were calculated and show high levels of variability throughout the campaign. This variability is affected by both changes in fire conditions, as fires tended to die down later in the measurement period, and by changes to the aerosol due to chemical reactions in the atmosphere.
S. Archer-Nicholls, D. Lowe, E. Darbyshire, W. T. Morgan, M. M. Bela, G. Pereira, J. Trembath, J. W. Kaiser, K. M. Longo, S. R. Freitas, H. Coe, and G. McFiggans
Geosci. Model Dev., 8, 549–577, https://doi.org/10.5194/gmd-8-549-2015, https://doi.org/10.5194/gmd-8-549-2015, 2015
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The regional WRF-Chem model was used to study aerosol particles from biomass burning in South America. The modelled estimates of fire plume injection heights were found to be too high, with serious implications for modelled aerosol vertical distribution, transport and impacts on local climate. A modified emission scenario was developed which improved the predicted injection height. Model results were compared and evaluated against in situ measurements from the 2012 SAMBBA flight campaign.
F. Pacifico, G. A. Folberth, S. Sitch, J. M. Haywood, L. V. Rizzo, F. F. Malavelle, and P. Artaxo
Atmos. Chem. Phys., 15, 2791–2804, https://doi.org/10.5194/acp-15-2791-2015, https://doi.org/10.5194/acp-15-2791-2015, 2015
D. E. Young, J. D. Allan, P. I. Williams, D. C. Green, R. M. Harrison, J. Yin, M. J. Flynn, M. W. Gallagher, and H. Coe
Atmos. Chem. Phys., 15, 2429–2443, https://doi.org/10.5194/acp-15-2429-2015, https://doi.org/10.5194/acp-15-2429-2015, 2015
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Two solid fuel organic aerosol (SFOA) factors, both associated with domestic space heating activities, were derived from positive matrix factorisation (PMF) applied to organic aerosol data from an aerosol mass spectrometer (AMS) deployed at an urban background site in London during winter 2012. The factors controlling the split between the two SFOA factors were assessed, and it is concluded the split is likely governed predominantly by differences in burn conditions.
S. Visser, J. G. Slowik, M. Furger, P. Zotter, N. Bukowiecki, R. Dressler, U. Flechsig, K. Appel, D. C. Green, A. H. Tremper, D. E. Young, P. I. Williams, J. D. Allan, S. C. Herndon, L. R. Williams, C. Mohr, L. Xu, N. L. Ng, A. Detournay, J. F. Barlow, C. H. Halios, Z. L. Fleming, U. Baltensperger, and A. S. H. Prévôt
Atmos. Chem. Phys., 15, 2367–2386, https://doi.org/10.5194/acp-15-2367-2015, https://doi.org/10.5194/acp-15-2367-2015, 2015
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Ambient concentrations of trace elements with 2h time resolution were measured in three size ranges (PM10–2.5, PM2.5–1.0, PM1.0–0.3) at kerbside, urban background and rural sites in London during the ClearfLo (Clean Air for London) field campaign. Quantification of kerb and urban increments, and assessment of diurnal and weekly variability provided insight into sources governing urban air quality and the effects of urban micro-environments on human exposure.
S. F. Kong, L. Li, X. X. Li, Y. Yin, K. Chen, D. T. Liu, L. Yuan, Y. J. Zhang, Y. P. Shan, and Y. Q. Ji
Atmos. Chem. Phys., 15, 2167–2184, https://doi.org/10.5194/acp-15-2167-2015, https://doi.org/10.5194/acp-15-2167-2015, 2015
J. Yin, S. A. Cumberland, R. M. Harrison, J. Allan, D. E. Young, P. I. Williams, and H. Coe
Atmos. Chem. Phys., 15, 2139–2158, https://doi.org/10.5194/acp-15-2139-2015, https://doi.org/10.5194/acp-15-2139-2015, 2015
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Breathing particles from polluted air is known to cause increased health complaints and higher death rates. Airborne particles come from a range of sources; in order to implement cost-effective control measures, it is necessary to understand the amount contributed by each. In this paper, two advanced procedures for estimating the contributions of particle sources in London are compared with one another, revealing a wide range of sources including traffic, woodsmoke and cooking particles.
K. M. Sakamoto, J. D. Allan, H. Coe, J. W. Taylor, T. J. Duck, and J. R. Pierce
Atmos. Chem. Phys., 15, 1633–1646, https://doi.org/10.5194/acp-15-1633-2015, https://doi.org/10.5194/acp-15-1633-2015, 2015
D. Lowe, S. Archer-Nicholls, W. Morgan, J. Allan, S. Utembe, B. Ouyang, E. Aruffo, M. Le Breton, R. A. Zaveri, P. Di Carlo, C. Percival, H. Coe, R. Jones, and G. McFiggans
Atmos. Chem. Phys., 15, 1385–1409, https://doi.org/10.5194/acp-15-1385-2015, https://doi.org/10.5194/acp-15-1385-2015, 2015
Y. J. Zhang, L. L. Tang, Z. Wang, H. X. Yu, Y. L. Sun, D. Liu, W. Qin, F. Canonaco, A. S. H. Prévôt, H. L. Zhang, and H. C. Zhou
Atmos. Chem. Phys., 15, 1331–1349, https://doi.org/10.5194/acp-15-1331-2015, https://doi.org/10.5194/acp-15-1331-2015, 2015
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The chemical composition, sources, and evolution processes of PM1 were investigated with an Aerodyne ACSM during harvest seasons in the Yangtze River delta, China. Two biomass burning organic aerosol (BBOA) factors derived from PMF model were assessed. The oxidized BBOA contributes ~80% of the total BBOA loadings in the BB plumes. Evidence that BBOA may be oxidized to more aged and less volatile organics during the aging process was suggested.
W. T. Morgan, B. Ouyang, J. D. Allan, E. Aruffo, P. Di Carlo, O. J. Kennedy, D. Lowe, M. J. Flynn, P. D. Rosenberg, P. I. Williams, R. Jones, G. B. McFiggans, and H. Coe
Atmos. Chem. Phys., 15, 973–990, https://doi.org/10.5194/acp-15-973-2015, https://doi.org/10.5194/acp-15-973-2015, 2015
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This paper used observations from a research aircraft flying around the UK to investigate how air pollution in north-western Europe can alter nighttime chemical reactions in the atmosphere. These chemical reactions can worsen air quality in the region, as well as influence regional climate change. Ammonium nitrate aerosol appears to play an important role. The paper indicates that representation of these chemical reactions is poorly represented in models used for air quality and climate.
J. W. Taylor, J. D. Allan, G. Allen, H. Coe, P. I. Williams, M. J. Flynn, M. Le Breton, J. B. A. Muller, C. J. Percival, D. Oram, G. Forster, J. D. Lee, A. R. Rickard, M. Parrington, and P. I. Palmer
Atmos. Chem. Phys., 14, 13755–13771, https://doi.org/10.5194/acp-14-13755-2014, https://doi.org/10.5194/acp-14-13755-2014, 2014
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We present a case study of BC wet removal by examining aerosol properties in three biomass burning plumes, one of which passed through a precipitating cloud. Nucleation scavenging preferentially removed the largest and most coated BC-containing particles. Calculated single-scattering albedo (SSA) showed little variation, as a large number of non-BC particles were also present in the precipitation-affected plume.
J. Brito, L. V. Rizzo, W. T. Morgan, H. Coe, B. Johnson, J. Haywood, K. Longo, S. Freitas, M. O. Andreae, and P. Artaxo
Atmos. Chem. Phys., 14, 12069–12083, https://doi.org/10.5194/acp-14-12069-2014, https://doi.org/10.5194/acp-14-12069-2014, 2014
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This paper details the physical--chemical characteristics of aerosols in a region strongly impacted by biomass burning in the western part of the Brazilian Amazon region. For such, a large suite of state-of-the-art instruments for realtime analysis was deployed at a ground site. Among the key findings, we observe the strong prevalence of organic aerosols associated to fire emissions, with important climate effects, and indications of its very fast processing in the atmosphere.
S. Decesari, J. Allan, C. Plass-Duelmer, B. J. Williams, M. Paglione, M. C. Facchini, C. O'Dowd, R. M. Harrison, J. K. Gietl, H. Coe, L. Giulianelli, G. P. Gobbi, C. Lanconelli, C. Carbone, D. Worsnop, A. T. Lambe, A. T. Ahern, F. Moretti, E. Tagliavini, T. Elste, S. Gilge, Y. Zhang, and M. Dall'Osto
Atmos. Chem. Phys., 14, 12109–12132, https://doi.org/10.5194/acp-14-12109-2014, https://doi.org/10.5194/acp-14-12109-2014, 2014
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We made use of multiple spectrometric techniques for characterizing the aerosol chemical composition and mixing in the Po Valley in the summer.
The oxygenated organic aerosol (OOA) concentrations were correlated with simple tracers for recirculated planetary boundary layer air.
A full internal mixing between black carbon (BC) and the non-refractory aerosol components was never observed. Local sources in the Po Valley were responsible for the production of organic particles unmixed with BC.
J. D. Whitehead, M. Irwin, J. D. Allan, N. Good, and G. McFiggans
Atmos. Chem. Phys., 14, 11833–11841, https://doi.org/10.5194/acp-14-11833-2014, https://doi.org/10.5194/acp-14-11833-2014, 2014
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Water uptake of ambient particles was measured by 2 independent techniques at a wide range of locations between 2007 and 2013. The agreement between the techniques was mixed and hence the number of potential cloud seeds calculated from the measurements frequently showed discrepancies. Whilst there is sensitivity to how well we measure the size of the particles, much of the difference depends on how the particles behave when exposed to moisture in the different techniques (and in the atmosphere).
S. Archer-Nicholls, D. Lowe, S. Utembe, J. Allan, R. A. Zaveri, J. D. Fast, Ø. Hodnebrog, H. Denier van der Gon, and G. McFiggans
Geosci. Model Dev., 7, 2557–2579, https://doi.org/10.5194/gmd-7-2557-2014, https://doi.org/10.5194/gmd-7-2557-2014, 2014
J. D. Allan, W. T. Morgan, E. Darbyshire, M. J. Flynn, P. I. Williams, D. E. Oram, P. Artaxo, J. Brito, J. D. Lee, and H. Coe
Atmos. Chem. Phys., 14, 11393–11407, https://doi.org/10.5194/acp-14-11393-2014, https://doi.org/10.5194/acp-14-11393-2014, 2014
X. Wang, C. L. Heald, D. A. Ridley, J. P. Schwarz, J. R. Spackman, A. E. Perring, H. Coe, D. Liu, and A. D. Clarke
Atmos. Chem. Phys., 14, 10989–11010, https://doi.org/10.5194/acp-14-10989-2014, https://doi.org/10.5194/acp-14-10989-2014, 2014
J. D. Fast, J. Allan, R. Bahreini, J. Craven, L. Emmons, R. Ferrare, P. L. Hayes, A. Hodzic, J. Holloway, C. Hostetler, J. L. Jimenez, H. Jonsson, S. Liu, Y. Liu, A. Metcalf, A. Middlebrook, J. Nowak, M. Pekour, A. Perring, L. Russell, A. Sedlacek, J. Seinfeld, A. Setyan, J. Shilling, M. Shrivastava, S. Springston, C. Song, R. Subramanian, J. W. Taylor, V. Vinoj, Q. Yang, R. A. Zaveri, and Q. Zhang
Atmos. Chem. Phys., 14, 10013–10060, https://doi.org/10.5194/acp-14-10013-2014, https://doi.org/10.5194/acp-14-10013-2014, 2014
D. Liu, J. D. Allan, D. E. Young, H. Coe, D. Beddows, Z. L. Fleming, M. J. Flynn, M. W. Gallagher, R. M. Harrison, J. Lee, A. S. H. Prevot, J. W. Taylor, J. Yin, P. I. Williams, and P. Zotter
Atmos. Chem. Phys., 14, 10061–10084, https://doi.org/10.5194/acp-14-10061-2014, https://doi.org/10.5194/acp-14-10061-2014, 2014
C. Fountoukis, A. G. Megaritis, K. Skyllakou, P. E. Charalampidis, C. Pilinis, H. A. C. Denier van der Gon, M. Crippa, F. Canonaco, C. Mohr, A. S. H. Prévôt, J. D. Allan, L. Poulain, T. Petäjä, P. Tiitta, S. Carbone, A. Kiendler-Scharr, E. Nemitz, C. O'Dowd, E. Swietlicki, and S. N. Pandis
Atmos. Chem. Phys., 14, 9061–9076, https://doi.org/10.5194/acp-14-9061-2014, https://doi.org/10.5194/acp-14-9061-2014, 2014
J. E. Franklin, J. R. Drummond, D. Griffin, J. R. Pierce, D. L. Waugh, P. I. Palmer, M. Parrington, J. D. Lee, A. C. Lewis, A. R. Rickard, J. W. Taylor, J. D. Allan, H. Coe, K. A. Walker, L. Chisholm, T. J. Duck, J. T. Hopper, Y. Blanchard, M. D. Gibson, K. R. Curry, K. M. Sakamoto, G. Lesins, L. Dan, J. Kliever, and A. Saha
Atmos. Chem. Phys., 14, 8449–8460, https://doi.org/10.5194/acp-14-8449-2014, https://doi.org/10.5194/acp-14-8449-2014, 2014
M. Crippa, F. Canonaco, V. A. Lanz, M. Äijälä, J. D. Allan, S. Carbone, G. Capes, D. Ceburnis, M. Dall'Osto, D. A. Day, P. F. DeCarlo, M. Ehn, A. Eriksson, E. Freney, L. Hildebrandt Ruiz, R. Hillamo, J. L. Jimenez, H. Junninen, A. Kiendler-Scharr, A.-M. Kortelainen, M. Kulmala, A. Laaksonen, A. A. Mensah, C. Mohr, E. Nemitz, C. O'Dowd, J. Ovadnevaite, S. N. Pandis, T. Petäjä, L. Poulain, S. Saarikoski, K. Sellegri, E. Swietlicki, P. Tiitta, D. R. Worsnop, U. Baltensperger, and A. S. H. Prévôt
Atmos. Chem. Phys., 14, 6159–6176, https://doi.org/10.5194/acp-14-6159-2014, https://doi.org/10.5194/acp-14-6159-2014, 2014
D. Stone, M. J. Evans, H. Walker, T. Ingham, S. Vaughan, B. Ouyang, O. J. Kennedy, M. W. McLeod, R. L. Jones, J. Hopkins, S. Punjabi, R. Lidster, J. F. Hamilton, J. D. Lee, A. C. Lewis, L. J. Carpenter, G. Forster, D. E. Oram, C. E. Reeves, S. Bauguitte, W. Morgan, H. Coe, E. Aruffo, C. Dari-Salisburgo, F. Giammaria, P. Di Carlo, and D. E. Heard
Atmos. Chem. Phys., 14, 1299–1321, https://doi.org/10.5194/acp-14-1299-2014, https://doi.org/10.5194/acp-14-1299-2014, 2014
S. Bezantakos, K. Barmpounis, M. Giamarelou, E. Bossioli, M. Tombrou, N. Mihalopoulos, K. Eleftheriadis, J. Kalogiros, J. D. Allan, A. Bacak, C. J. Percival, H. Coe, and G. Biskos
Atmos. Chem. Phys., 13, 11595–11608, https://doi.org/10.5194/acp-13-11595-2013, https://doi.org/10.5194/acp-13-11595-2013, 2013
J. F. Hamilton, M. R. Alfarra, N. Robinson, M. W. Ward, A. C. Lewis, G. B. McFiggans, H. Coe, and J. D. Allan
Atmos. Chem. Phys., 13, 11295–11305, https://doi.org/10.5194/acp-13-11295-2013, https://doi.org/10.5194/acp-13-11295-2013, 2013
R. Saleh, C. J. Hennigan, G. R. McMeeking, W. K. Chuang, E. S. Robinson, H. Coe, N. M. Donahue, and A. L. Robinson
Atmos. Chem. Phys., 13, 7683–7693, https://doi.org/10.5194/acp-13-7683-2013, https://doi.org/10.5194/acp-13-7683-2013, 2013
M. Parrington, P. I. Palmer, A. C. Lewis, J. D. Lee, A. R. Rickard, P. Di Carlo, J. W. Taylor, J. R. Hopkins, S. Punjabi, D. E. Oram, G. Forster, E. Aruffo, S. J. Moller, S. J.-B. Bauguitte, J. D. Allan, H. Coe, and R. J. Leigh
Atmos. Chem. Phys., 13, 7321–7341, https://doi.org/10.5194/acp-13-7321-2013, https://doi.org/10.5194/acp-13-7321-2013, 2013
P. J. Connolly, G. Vaughan, P. Cook, G. Allen, H. Coe, T. W. Choularton, C. Dearden, and A. Hill
Atmos. Chem. Phys., 13, 7133–7152, https://doi.org/10.5194/acp-13-7133-2013, https://doi.org/10.5194/acp-13-7133-2013, 2013
C. L. Reddington, G. McMeeking, G. W. Mann, H. Coe, M. G. Frontoso, D. Liu, M. Flynn, D. V. Spracklen, and K. S. Carslaw
Atmos. Chem. Phys., 13, 4917–4939, https://doi.org/10.5194/acp-13-4917-2013, https://doi.org/10.5194/acp-13-4917-2013, 2013
C. A. Randles, S. Kinne, G. Myhre, M. Schulz, P. Stier, J. Fischer, L. Doppler, E. Highwood, C. Ryder, B. Harris, J. Huttunen, Y. Ma, R. T. Pinker, B. Mayer, D. Neubauer, R. Hitzenberger, L. Oreopoulos, D. Lee, G. Pitari, G. Di Genova, J. Quaas, F. G. Rose, S. Kato, S. T. Rumbold, I. Vardavas, N. Hatzianastassiou, C. Matsoukas, H. Yu, F. Zhang, H. Zhang, and P. Lu
Atmos. Chem. Phys., 13, 2347–2379, https://doi.org/10.5194/acp-13-2347-2013, https://doi.org/10.5194/acp-13-2347-2013, 2013
D. Liu, J. Allan, J. Whitehead, D. Young, M. Flynn, H. Coe, G. McFiggans, Z. L. Fleming, and B. Bandy
Atmos. Chem. Phys., 13, 2015–2029, https://doi.org/10.5194/acp-13-2015-2013, https://doi.org/10.5194/acp-13-2015-2013, 2013
N. H. Robinson, J. D. Allan, J. A. Huffman, P. H. Kaye, V. E. Foot, and M. Gallagher
Atmos. Meas. Tech., 6, 337–347, https://doi.org/10.5194/amt-6-337-2013, https://doi.org/10.5194/amt-6-337-2013, 2013
L. Guo, E. J. Highwood, L. C. Shaffrey, and A. G. Turner
Atmos. Chem. Phys., 13, 1521–1534, https://doi.org/10.5194/acp-13-1521-2013, https://doi.org/10.5194/acp-13-1521-2013, 2013
G. E. Thomas, N. Chalmers, B. Harris, R. G. Grainger, and E. J. Highwood
Atmos. Chem. Phys., 13, 393–410, https://doi.org/10.5194/acp-13-393-2013, https://doi.org/10.5194/acp-13-393-2013, 2013
C. L. Ryder, E. J. Highwood, P. D. Rosenberg, J. Trembath, J. K. Brooke, M. Bart, A. Dean, J. Crosier, J. Dorsey, H. Brindley, J. Banks, J. H. Marsham, J. B. McQuaid, H. Sodemann, and R. Washington
Atmos. Chem. Phys., 13, 303–325, https://doi.org/10.5194/acp-13-303-2013, https://doi.org/10.5194/acp-13-303-2013, 2013
M. Laborde, M. Schnaiter, C. Linke, H. Saathoff, K.-H. Naumann, O. Möhler, S. Berlenz, U. Wagner, J. W. Taylor, D. Liu, M. Flynn, J. D. Allan, H. Coe, K. Heimerl, F. Dahlkötter, B. Weinzierl, A. G. Wollny, M. Zanatta, J. Cozic, P. Laj, R. Hitzenberger, J. P. Schwarz, and M. Gysel
Atmos. Meas. Tech., 5, 3077–3097, https://doi.org/10.5194/amt-5-3077-2012, https://doi.org/10.5194/amt-5-3077-2012, 2012
T. Hamburger, G. McMeeking, A. Minikin, A. Petzold, H. Coe, and R. Krejci
Atmos. Chem. Phys., 12, 11533–11554, https://doi.org/10.5194/acp-12-11533-2012, https://doi.org/10.5194/acp-12-11533-2012, 2012
Related subject area
Subject: Aerosols | Research Activity: Field Measurements | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Linking marine phytoplankton emissions, meteorological processes, and downwind particle properties with FLEXPART
Highly time-resolved measurements of element concentrations in PM10 and PM2.5: comparison of Delhi, Beijing, London, and Krakow
Atmospheric evolution of emissions from a boreal forest fire: the formation of highly functionalized oxygen-, nitrogen-, and sulfur-containing organic compounds
Concerted measurements of free amino acids at the Cabo Verde islands: high enrichments in submicron sea spray aerosol particles and cloud droplets
Investigating three patterns of new particles growing to the size of cloud condensation nuclei in Beijing's urban atmosphere
Measurement report: dual-carbon isotopic characterization of carbonaceous aerosol reveals different primary and secondary sources in Beijing and Xi'an during severe haze events
North Atlantic marine organic aerosol characterized by novel offline thermal desorption mass spectrometry: polysaccharides, recalcitrant material, and secondary organics
Sources and characteristics of size-resolved particulate organic acids and methanesulfonate in a coastal megacity: Manila, Philippines
Effects of AIR pollution on cardiopuLmonary disEaSe in urban and peri-urban reSidents in Beijing: protocol for the AIRLESS study
Chemical composition and source apportionment of atmospheric aerosols on the Namibian coast
Exploring the drivers of the increased ozone production in Beijing in summertime during 2005–2016
Optical source apportionment and radiative effect of light-absorbing carbonaceous aerosols in a tropical marine monsoon climate zone: the importance of ship emissions
Measurement report: Seasonality, distribution and sources of organophosphate esters in PM2.5 from an inland urban city in Southwest China
Nationwide increase of polycyclic aromatic hydrocarbons in ultrafine particles during winter over China revealed by size-segregated measurements
Size-resolved exposure risk of persistent free radicals (PFRs) in atmospheric aerosols and their potential sources
Source apportionment of black carbon aerosols from light absorption observation and source-oriented modeling: an implication in a coastal city in China
Tracing the evolution of morphology and mixing state of soot particles along with the movement of an Asian dust storm
A comparison of PM2.5-bound polycyclic aromatic hydrocarbons in summer Beijing (China) and Delhi (India)
Impact of in-cloud aqueous processes on the chemical compositions and morphology of individual atmospheric aerosols
Tropospheric aerosol hygroscopicity in China
Investigation of the wet removal rate of black carbon in East Asia: validation of a below- and in-cloud wet removal scheme in FLEXible PARTicle (FLEXPART) model v10.4
Differences in the composition of organic aerosols between winter and summer in Beijing: a study by direct-infusion ultrahigh-resolution mass spectrometry
The promotion effect of nitrous acid on aerosol formation in wintertime in Beijing: the possible contribution of traffic-related emissions
Sulfuric acid-amine nucleation in urban Beijing
Size-segregated particle number and mass concentrations from different emission sources in urban Beijing
Source apportionment of PM2.5 in Shanghai based on hourly organic molecular markers and other source tracers
Mixing states of Amazon basin aerosol particles transported over long distances using transmission electron microscopy
Persistent primary organic tar particles during the regional wintertime hazes in North China: insights into their aging and optical changes
Differences in fine particle chemical composition on clear and cloudy days
Optical properties and composition of viscous organic particles found in the Southern Great Plains
Measurement report: Chemical characteristics of PM2.5 during typical biomass burning season at an agricultural site of the North China Plain
Measurement report: Characterization of severe spring haze episodes and influences of long-range transport in the Seoul metropolitan area in March 2019
Modeling the smoky troposphere of the southeast Atlantic: a comparison to ORACLES airborne observations from September of 2016
Formation and sink of glyoxal and methylglyoxal in a polluted subtropical environment: observation-based photochemical analysis and impact evaluation
Hygroscopicity of urban aerosols and its link to size-resolved chemical composition during spring and summer in Seoul, Korea
Elucidating the pollution characteristics of nitrate, sulfate and ammonium in PM2.5 in Chengdu, southwest China, based on 3-year measurements
Measurement report: PM2.5-bound nitrated aromatic compounds in Xi'an, Northwest China: Seasonal variations and contributions to optical properties of brown carbon
The impact of traffic on air quality in Ireland: insights from the simultaneous kerbside and suburban monitoring of submicron aerosols
Vertical distribution of particle-phase dicarboxylic acids, oxoacids and α-dicarbonyls in the urban boundary layer based on the 325 m tower in Beijing
Characterization and source apportionment of aerosol light scattering in a typical polluted city in the Yangtze River Delta, China
Molecular insights into new particle formation in Barcelona, Spain
Concentrations, Particle-Size Distributions, and Dry Deposition Fluxes of Aerosol Trace Elements over the Antarctic Peninsula
Tracking separate contributions of diesel and gasoline vehicles to roadside PM2.5 through online monitoring of volatile organic compounds and PM2.5 organic and elemental carbon: a 6-year study in Hong Kong
Measurement report: Effects of photochemical aging on the formation and evolution of summertime secondary aerosol in Beijing
Probing key organic substances driving new particle growth initiated by iodine nucleation in coastal atmosphere
Variations in Ncn and Nccn over marginal seas in China related to marine traffic emissions, new particle formation and aerosol aging
Characteristics, primary sources and secondary formation of water soluble organic aerosols in downtown Beijing
Simultaneous measurements of urban and rural particles in Beijing – Part 1: Chemical composition and mixing state
Simultaneous measurements of urban and rural particles in Beijing – Part 2: Case studies of haze events and regional transport
Ship plumes in the Baltic Sea Sulfur Emission Control Area: chemical characterization and contribution to coastal aerosol concentrations
Kevin J. Sanchez, Bo Zhang, Hongyu Liu, Georges Saliba, Chia-Li Chen, Savannah L. Lewis, Lynn M. Russell, Michael A. Shook, Ewan C. Crosbie, Luke D. Ziemba, Matthew D. Brown, Taylor J. Shingler, Claire E. Robinson, Elizabeth B. Wiggins, Kenneth L. Thornhill, Edward L. Winstead, Carolyn Jordan, Patricia K. Quinn, Timothy S. Bates, Jack Porter, Thomas G. Bell, Eric S. Saltzman, Michael J. Behrenfeld, and Richard H. Moore
Atmos. Chem. Phys., 21, 831–851, https://doi.org/10.5194/acp-21-831-2021, https://doi.org/10.5194/acp-21-831-2021, 2021
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Models describing atmospheric airflow were combined with satellite measurements representative of marine phytoplankton and other meteorological variables. These combined variables were compared to measured aerosol to identify upwind influences on aerosol concentrations. Results indicate that phytoplankton production rates upwind impact the aerosol mass. Also, results suggest that the condensation of mass onto short-lived large sea spray particles may be a significant sink of aerosol mass.
Pragati Rai, Jay G. Slowik, Markus Furger, Imad El Haddad, Suzanne Visser, Yandong Tong, Atinderpal Singh, Günther Wehrle, Varun Kumar, Anna K. Tobler, Deepika Bhattu, Liwei Wang, Dilip Ganguly, Neeraj Rastogi, Ru-Jin Huang, Jaroslaw Necki, Junji Cao, Sachchida N. Tripathi, Urs Baltensperger, and André S. H. Prévôt
Atmos. Chem. Phys., 21, 717–730, https://doi.org/10.5194/acp-21-717-2021, https://doi.org/10.5194/acp-21-717-2021, 2021
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We present a simple conceptual framework based on elemental size distributions and enrichment factors that allows for a characterization of major sources, site-to-site similarities, and local differences and the identification of key information required for efficient policy development. Absolute concentrations are by far the highest in Delhi, followed by Beijing, and then the European cities.
Jenna C. Ditto, Megan He, Tori N. Hass-Mitchell, Samar G. Moussa, Katherine Hayden, Shao-Meng Li, John Liggio, Amy Leithead, Patrick Lee, Michael J. Wheeler, Jeremy J. B. Wentzell, and Drew R. Gentner
Atmos. Chem. Phys., 21, 255–267, https://doi.org/10.5194/acp-21-255-2021, https://doi.org/10.5194/acp-21-255-2021, 2021
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Forest fires are an important source of reactive organic gases and aerosols to the atmosphere. We analyzed organic aerosols collected from an aircraft above a boreal forest fire and reported an increasing contribution from compounds containing oxygen, nitrogen, and sulfur as the plume aged, with sulfide and ring-bound nitrogen functionality. Our results demonstrated chemistry that is important in biomass burning but also in urban/developing regions with high local nitrogen and sulfur emissions.
Nadja Triesch, Manuela van Pinxteren, Anja Engel, and Hartmut Herrmann
Atmos. Chem. Phys., 21, 163–181, https://doi.org/10.5194/acp-21-163-2021, https://doi.org/10.5194/acp-21-163-2021, 2021
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To investigate the sources of free amino acids (FAAs) in the marine atmosphere, concerted measurements (the simultaneous investigation of seawater, size-segregated aerosol particles and cloud water) were performed at the Cabo Verde islands. This study describes the transfer of FAAs as part of organic matter from the ocean into the atmosphere on a molecular level. In the investigated marine environment, a high enrichment of FAAs in submicron aerosol particles and in cloud droplets was observed.
Liya Ma, Yujiao Zhu, Mei Zheng, Yele Sun, Lei Huang, Xiaohuan Liu, Yang Gao, Yanjie Shen, Huiwang Gao, and Xiaohong Yao
Atmos. Chem. Phys., 21, 183–200, https://doi.org/10.5194/acp-21-183-2021, https://doi.org/10.5194/acp-21-183-2021, 2021
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In this study, we investigate three patterns of new particles growing to CCN (cloud condensation nuclei) size, i.e., one-stage growth and two-stage growth-A and growth-B patterns. Combining the observations of gaseous pollutants and measured or modeled particulate chemical species, the three growth patterns were discussed regarding the spatial heterogeneity, formation of secondary aerosols, and evaporation of semivolatile particulates as was the survival probability of new particles to CCN size.
Haiyan Ni, Ru-Jin Huang, Max M. Cosijn, Lu Yang, Jie Guo, Junji Cao, and Ulrike Dusek
Atmos. Chem. Phys., 20, 16041–16053, https://doi.org/10.5194/acp-20-16041-2020, https://doi.org/10.5194/acp-20-16041-2020, 2020
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We investigated sources of carbonaceous aerosols in Beijing and Xi'an during severe winter haze. Elemental carbon (EC) was dominated by vehicle emissions in Xi’an and coal burning in Beijing. Organic carbon (OC) increment during haze days was driven by the increase in primary and secondary OC (SOC). SOC was more from fossil sources in Beijing than Xi’an, especially during haze days. In Xi’an, no strong day–night differences in EC or OC sources suggest a large accumulation of particles.
Michael J. Lawler, Savannah L. Lewis, Lynn M. Russell, Patricia K. Quinn, Timothy S. Bates, Derek J. Coffman, Lucia M. Upchurch, and Eric S. Saltzman
Atmos. Chem. Phys., 20, 16007–16022, https://doi.org/10.5194/acp-20-16007-2020, https://doi.org/10.5194/acp-20-16007-2020, 2020
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This work describes new measurements of aerosol (particles) composition over the North Atlantic Ocean. It provides concentrations of polysaccharide material likely made from organisms in the surface ocean and improves our understanding of the relative importance of such fresh biogenic material compared to more recalcitrant organic carbon in forming marine organic aerosol. We aim ultimately to understand the role that ocean biology plays in cloud formation in marine regions.
Connor Stahl, Melliza Templonuevo Cruz, Paola Angela Bañaga, Grace Betito, Rachel A. Braun, Mojtaba Azadi Aghdam, Maria Obiminda Cambaliza, Genevieve Rose Lorenzo, Alexander B. MacDonald, Miguel Ricardo A. Hilario, Preciosa Corazon Pabroa, John Robin Yee, James Bernard Simpas, and Armin Sorooshian
Atmos. Chem. Phys., 20, 15907–15935, https://doi.org/10.5194/acp-20-15907-2020, https://doi.org/10.5194/acp-20-15907-2020, 2020
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Long-term (16-month) high-frequency (weekly) measurements of size-resolved aerosol composition are reported. Important insights are discussed about factors (e.g., transport, fires, precipitation, photo-oxidation) impacting the mass size distributions of organic and sulfonic acids at a coastal megacity with diverse meteorology. The size-resolved nature of the data yielded one such finding that organic acids preferentially adsorb to dust rather than sea salt particles.
Yiqun Han, Wu Chen, Lia Chatzidiakou, Anika Krause, Li Yan, Hanbin Zhang, Queenie Chan, Ben Barratt, Rod Jones, Jing Liu, Yangfeng Wu, Meiping Zhao, Junfeng Zhang, Frank J. Kelly, Tong Zhu, and the AIRLESS team
Atmos. Chem. Phys., 20, 15775–15792, https://doi.org/10.5194/acp-20-15775-2020, https://doi.org/10.5194/acp-20-15775-2020, 2020
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Panel studies might be the most suitable way to link intensive air monitoring campaigns for a wide range of pollutant species and personal exposure in different micro-environments, together with epidemiological studies of detailed biological changes in humans. Panel studies are intensive, but related papers are very limited. With the successful collection of a rich dataset, we believe AIRLESS sets a good example for the design of a multidisciplinary study.
Danitza Klopper, Paola Formenti, Andreas Namwoonde, Mathieu Cazaunau, Servanne Chevaillier, Anaïs Feron, Cécile Gaimoz, Patrick Hease, Fadi Lahmidi, Cécile Mirande-Bret, Sylvain Triquet, Zirui Zeng, and Stuart J. Piketh
Atmos. Chem. Phys., 20, 15811–15833, https://doi.org/10.5194/acp-20-15811-2020, https://doi.org/10.5194/acp-20-15811-2020, 2020
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The chemical composition of aerosol particles is very important as it determines to which extent they can affect the Earth's climate by acting with solar light and modifying the properties of clouds. The South Atlantic region is a remote and under-explored region to date where these effects could be important. The measurements presented in this paper consist in the analysis of samples collected at a coastal site in Namibia. The first long-term source apportionment is presented and discussed.
Wenjie Wang, David D. Parrish, Xin Li, Min Shao, Ying Liu, Ziwei Mo, Sihua Lu, Min Hu, Xin Fang, Yusheng Wu, Limin Zeng, and Yuanhang Zhang
Atmos. Chem. Phys., 20, 15617–15633, https://doi.org/10.5194/acp-20-15617-2020, https://doi.org/10.5194/acp-20-15617-2020, 2020
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During the past decade, China has devoted very substantial resources to improving the environment. These efforts have improved atmospheric particulate matter loading, but ambient ozone levels have continued to increase. In this paper we investigate the causes of the increasing ozone concentrations through analysis of a data set that is, to our knowledge, unique: a 12-year data set including ground-level O3, NOx, and VOC precursors collected at an urban site in Beijing.
Qiyuan Wang, Huikun Liu, Ping Wang, Wenting Dai, Ting Zhang, Youzhi Zhao, Jie Tian, Wenyan Zhang, Yongming Han, and Junji Cao
Atmos. Chem. Phys., 20, 15537–15549, https://doi.org/10.5194/acp-20-15537-2020, https://doi.org/10.5194/acp-20-15537-2020, 2020
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Light-absorbing carbonaceous (LAC) aerosol is an important influencing factor for global climate forcing. In this study, we used a receptor model coupling multi-wavelength absorption with chemical species to explore the source-specific LAC optical properties at a tropical marine monsoon climate zone. The results can improve our understanding of the LAC radiative effects caused by ship emissions.
Hongling Yin, Jinfeng Liang, Di Wu, Shiping Li, Yi Luo, and Xu Deng
Atmos. Chem. Phys., 20, 14933–14945, https://doi.org/10.5194/acp-20-14933-2020, https://doi.org/10.5194/acp-20-14933-2020, 2020
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Samples were collected from six ground-based sites located in Chengdu, a typical rapidly developing metropolitan area in Southwest China, and were analysed for seven OPEs in atmospheric PM2.5 (Σ7 OPEs). The concentrations of Σ7 OPEs were higher in autumn and winter than in summer. In contrast to coastal cities, sustained and stable high local emissions in the inland city studied were identified, which is particularly noteworthy.
Qingqing Yu, Xiang Ding, Quanfu He, Weiqiang Yang, Ming Zhu, Sheng Li, Runqi Zhang, Ruqin Shen, Yanli Zhang, Xinhui Bi, Yuesi Wang, Ping'an Peng, and Xinming Wang
Atmos. Chem. Phys., 20, 14581–14595, https://doi.org/10.5194/acp-20-14581-2020, https://doi.org/10.5194/acp-20-14581-2020, 2020
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We carried out a 1-year PM concurrent observation at 12 sites across six regions of China, and size-segregated PAHs were measured. We found both PAHs and BaPeq were concentrated in PM1.1, and northern China had higher PAHs' pollution and inhalation cancer risk than southern China. Nationwide increases in both PAH levels and inhalation cancer risk occurred in winter. We suggest reducing coal and biofuel consumption in the residential sector is an important option to mitigate PAHs' health risks.
Qingcai Chen, Haoyao Sun, Wenhuai Song, Fang Cao, Chongguo Tian, and Yan-Lin Zhang
Atmos. Chem. Phys., 20, 14407–14417, https://doi.org/10.5194/acp-20-14407-2020, https://doi.org/10.5194/acp-20-14407-2020, 2020
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This study found environmentally persistent free radicals (EPFRs) are widely present in atmospheric particles of different particle sizes and exhibit significant particle size distribution characteristics. EPFR concentrations are higher in coarse particles than in fine particles in summer and vice versa in winter. The potential toxicity caused by EPFRs may also vary with particle size and season. Combustion is the most important source of EPFRs (>70 %).
Junjun Deng, Hao Guo, Hongliang Zhang, Jialei Zhu, Xin Wang, and Pingqing Fu
Atmos. Chem. Phys., 20, 14419–14435, https://doi.org/10.5194/acp-20-14419-2020, https://doi.org/10.5194/acp-20-14419-2020, 2020
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One-year source apportionment of BC aerosols in a coastal city in China was conducted with the light-absorption observation-based method and source-oriented model. Source contributions identified by the two source apportionment methods were compared. Temporal variability, potential sources and transport pathways of BC from fossil fuel and biomass burning were characterized. Significant influence of biomass burning in North and East–Central China on BC in the region was highlighted.
Liang Xu, Satoshi Fukushima, Sophie Sobanska, Kotaro Murata, Ayumi Naganuma, Lei Liu, Yuanyuan Wang, Hongya Niu, Zongbo Shi, Tomoko Kojima, Daizhou Zhang, and Weijun Li
Atmos. Chem. Phys., 20, 14321–14332, https://doi.org/10.5194/acp-20-14321-2020, https://doi.org/10.5194/acp-20-14321-2020, 2020
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We quantified the mixing structures of soot particles and found that the dominant mixing structure changed from fresh to partially embedded to fully embedded along the pathway of an Asian dust storm from eastern China to Japan. Soot particles became more compact following transport. Our findings not only provide direct evidence for soot aging during regional transport but also help us understand how their morphology changes in different air environments.
Atallah Elzein, Gareth J. Stewart, Stefan J. Swift, Beth S. Nelson, Leigh R. Crilley, Mohammed S. Alam, Ernesto Reyes-Villegas, Ranu Gadi, Roy M. Harrison, Jacqueline F. Hamilton, and Alastair C. Lewis
Atmos. Chem. Phys., 20, 14303–14319, https://doi.org/10.5194/acp-20-14303-2020, https://doi.org/10.5194/acp-20-14303-2020, 2020
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We collected high-frequency air particle samples (PM2.5) in Beijing (China) and Delhi (India) and measured the concentration of PAHs in daytime and night-time. PAHs were higher in Delhi than in Beijing, and the five-ring PAHs contribute the most to the total PAH concentration. We compared the emission sources and identified the major sectors that could be subject to mitigation measures. The adverse health effects from inhalation exposure to PAHs in Delhi are 2.2 times higher than in Beijing.
Yuzhen Fu, Qinhao Lin, Guohua Zhang, Yuxiang Yang, Yiping Yang, Xiufeng Lian, Long Peng, Feng Jiang, Xinhui Bi, Lei Li, Yuanyuan Wang, Duohong Chen, Jie Ou, Xinming Wang, Ping'an Peng, Jianxi Zhu, and Guoying Sheng
Atmos. Chem. Phys., 20, 14063–14075, https://doi.org/10.5194/acp-20-14063-2020, https://doi.org/10.5194/acp-20-14063-2020, 2020
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Based on the analysis of the morphology and mixing structure of the activated and unactivated particles, our results emphasize the role of in-cloud processes in the chemistry and microphysical properties of individual activated particles. Given that organic coatings may determine the particle hygroscopicity and heterogeneous chemical reactivity, the increase of OM-shelled particles upon in-cloud processes should have considerable implications for their evolution and climate impact.
Chao Peng, Yu Wang, Zhijun Wu, Lanxiadi Chen, Ru-Jin Huang, Weigang Wang, Zhe Wang, Weiwei Hu, Guohua Zhang, Maofa Ge, Min Hu, Xinming Wang, and Mingjin Tang
Atmos. Chem. Phys., 20, 13877–13903, https://doi.org/10.5194/acp-20-13877-2020, https://doi.org/10.5194/acp-20-13877-2020, 2020
Yongjoo Choi, Yugo Kanaya, Masayuki Takigawa, Chunmao Zhu, Seung-Myung Park, Atsushi Matsuki, Yasuhiro Sadanaga, Sang-Woo Kim, Xiaole Pan, and Ignacio Pisso
Atmos. Chem. Phys., 20, 13655–13670, https://doi.org/10.5194/acp-20-13655-2020, https://doi.org/10.5194/acp-20-13655-2020, 2020
Sarah S. Steimer, Daniel J. Patton, Tuan V. Vu, Marios Panagi, Paul S. Monks, Roy M. Harrison, Zoë L. Fleming, Zongbo Shi, and Markus Kalberer
Atmos. Chem. Phys., 20, 13303–13318, https://doi.org/10.5194/acp-20-13303-2020, https://doi.org/10.5194/acp-20-13303-2020, 2020
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Air pollution is of growing concern due to its negative effect on public health, especially in low- and middle-income countries. This study investigates how the chemical composition of particles in Beijing changes under different measurement conditions (pollution levels, season) to get a better understanding of the sources of this form of air pollution.
Yongchun Liu, Yusheng Zhang, Chaofan Lian, Chao Yan, Zeming Feng, Feixue Zheng, Xiaolong Fan, Yan Chen, Weigang Wang, Biwu Chu, Yonghong Wang, Jing Cai, Wei Du, Kaspar R. Daellenbach, Juha Kangasluoma, Federico Bianchi, Joni Kujansuu, Tuukka Petäjä, Xuefei Wang, Bo Hu, Yuesi Wang, Maofa Ge, Hong He, and Markku Kulmala
Atmos. Chem. Phys., 20, 13023–13040, https://doi.org/10.5194/acp-20-13023-2020, https://doi.org/10.5194/acp-20-13023-2020, 2020
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Understanding of the chemical and physical processes leading to atmospheric aerosol particle formation is crucial to devising effective mitigation strategies to protect the public and reduce uncertainties in climate predictions. We found that the photolysis of nitrous acid could promote the formation of organic and nitrate aerosol and that traffic-related emission is a major contributor to ambient nitrous acid on haze days in wintertime in Beijing.
Runlong Cai, Chao Yan, Dongsen Yang, Rujing Yin, Yiqun Lu, Chenjuan Deng, Yueyun Fu, Jiaxin Ruan, Xiaoxiao Li, Jenni Kontkanen, Qiang Zhang, Juha Kangasluoma, Yan Ma, Jiming Hao, Douglas R. Worsnop, Federico Bianchi, Pauli Paasonen, Veli-Matti Kerminen, Yongchun Liu, Lin Wang, Jun Zheng, Markku Kulmala, and Jingkun Jiang
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2020-1060, https://doi.org/10.5194/acp-2020-1060, 2020
Revised manuscript accepted for ACP
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Based on long-term measurements, we discovered that the collision of H2SO4-amine clusters is the governing mechanism that initializes fast new particle formation in the polluted atmospheric environment of urban Beijing. The mechanism and the governing factors for H2SO4-amine nucleation in the polluted atmosphere are quantitatively investigated in this study.
Jing Cai, Biwu Chu, Lei Yao, Chao Yan, Liine M. Heikkinen, Feixue Zheng, Chang Li, Xiaolong Fan, Shaojun Zhang, Daoyuan Yang, Yonghong Wang, Tom V. Kokkonen, Tommy Chan, Ying Zhou, Lubna Dada, Yongchun Liu, Hong He, Pauli Paasonen, Joni T. Kujansuu, Tuukka Petäjä, Claudia Mohr, Juha Kangasluoma, Federico Bianchi, Yele Sun, Philip L. Croteau, Douglas R. Worsnop, Veli-Matti Kerminen, Wei Du, Markku Kulmala, and Kaspar R. Daellenbach
Atmos. Chem. Phys., 20, 12721–12740, https://doi.org/10.5194/acp-20-12721-2020, https://doi.org/10.5194/acp-20-12721-2020, 2020
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By applying both OA PMF and size PMF at the same urban measurement site in Beijing, similar particle source types, including vehicular emissions, cooking emissions and secondary formation-related sources, were resolved by both frameworks and agreed well. It is also found that in the absence of new particle formation, vehicular and cooking emissions dominate the particle number concentration, while secondary particulate matter governed PM2.5 mass during spring and summer in Beijing.
Rui Li, Qiongqiong Wang, Xiao He, Shuhui Zhu, Kun Zhang, Yusen Duan, Qingyan Fu, Liping Qiao, Yangjun Wang, Ling Huang, Li Li, and Jian Zhen Yu
Atmos. Chem. Phys., 20, 12047–12061, https://doi.org/10.5194/acp-20-12047-2020, https://doi.org/10.5194/acp-20-12047-2020, 2020
Kouji Adachi, Naga Oshima, Zhaoheng Gong, Suzane de Sá, Adam P. Bateman, Scot T. Martin, Joel F. de Brito, Paulo Artaxo, Glauber G. Cirino, Arthur J. Sedlacek III, and Peter R. Buseck
Atmos. Chem. Phys., 20, 11923–11939, https://doi.org/10.5194/acp-20-11923-2020, https://doi.org/10.5194/acp-20-11923-2020, 2020
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Occurrences, size distributions, and number fractions of individual aerosol particles from the Amazon basin during the GoAmazon2014/5 campaign were analyzed using transmission electron microscopy. Aerosol particles from natural sources (e.g., mineral dust, primary biological aerosols, and sea salts) during the wet season originated from the Amazon forest and long-range transports (the Saharan desert and the Atlantic Ocean). They commonly mix at an individual particle scale during transport.
Lei Liu, Jian Zhang, Yinxiao Zhang, Yuanyuan Wang, Liang Xu, Qi Yuan, Dantong Liu, Yele Sun, Pingqing Fu, Zongbo Shi, and Weijun Li
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2020-1012, https://doi.org/10.5194/acp-2020-1012, 2020
Revised manuscript accepted for ACP
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This study found that a distinct group of primary organic particles with high viscosity emitted from the domestic coal and biomass burning, defined as primary organic tar (POT) particles, were abundant in the rural and even the urban haze in winter of North China. For the first time, we characterized the atmospheric aging process of POT particles by microscopic analysis and further evaluated their light absorption enhancement due to the
lensing effectsof secondary inorganic coatings.
Amy E. Christiansen, Annmarie G. Carlton, and Barron H. Henderson
Atmos. Chem. Phys., 20, 11607–11624, https://doi.org/10.5194/acp-20-11607-2020, https://doi.org/10.5194/acp-20-11607-2020, 2020
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We quantify differences in surface-level fine particle mass (PM2.5) chemical composition in relation to satellite-derived cloud flags and find significant differences between clear-sky and cloud days. The work suggests that future analysis in this area is warranted.
Matthew Fraund, Daniel J. Bonanno, Swarup China, Don Q. Pham, Daniel Veghte, Johannes Weis, Gourihar Kulkarni, Ken Teske, Mary K. Gilles, Alexander Laskin, and Ryan C. Moffet
Atmos. Chem. Phys., 20, 11593–11606, https://doi.org/10.5194/acp-20-11593-2020, https://doi.org/10.5194/acp-20-11593-2020, 2020
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High viscosity organic particles (HVOPs) in the Southern Great Plains have been analyzed, and two particle types were found. Previously studied tar balls and the recently discovered airborne soil organic particles (ASOPs) are both shown to be brown carbon (BrC). These particle types can be identified in bulk by an absorption Ångström exponent approaching 2.6. HVOP types can be differentiated by comparing carbon absorption spectrum peak ratios between the carboxylic acid, alcohol, and sp2 peaks.
Linlin Liang, Guenter Engling, Chang Liu, Wanyun Xu, Xuyan Liu, Yuan Cheng, Zhenyu Du, Gen Zhang, Junying Sun, and Xiaoye Zhang
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2020-1006, https://doi.org/10.5194/acp-2020-1006, 2020
Revised manuscript accepted for ACP
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A unique episode with extreme biomass burning (BB) impact, with daily concentration of levoglucosan as high as 4.37 µg m−3, was captured at an upwind area of Beijing. How this extreme BB pollution event generated and how about the chemical properties of PM2.5 under this kind severe BB pollution level in the real atmospheric environment, were both presented in this measurement report. Moreover, the variation of the ratios of BB tracers during different BB pollution periods was also exhibited.
Hwajin Kim, Qi Zhang, and Yele Sun
Atmos. Chem. Phys., 20, 11527–11550, https://doi.org/10.5194/acp-20-11527-2020, https://doi.org/10.5194/acp-20-11527-2020, 2020
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Severe spring haze and influences of long-range transport in the Seoul metropolitan area (SMA) in March 2019 were investigated. Simultaneous downwind (SMA) and upwind (Beijing) measurements using AMS and ACSM over the same period showed that PM species can be transported in approximately 2 d. Nitrate was the most responsible, and sulfate and two regional-transport-influenced SOAs also contributed. Enhancement of Pb also showed that the haze in the SMA was influenced by the regional transport.
Yohei Shinozuka, Pablo E. Saide, Gonzalo A. Ferrada, Sharon P. Burton, Richard Ferrare, Sarah J. Doherty, Hamish Gordon, Karla Longo, Marc Mallet, Yan Feng, Qiaoqiao Wang, Yafang Cheng, Amie Dobracki, Steffen Freitag, Steven G. Howell, Samuel LeBlanc, Connor Flynn, Michal Segal-Rosenhaimer, Kristina Pistone, James R. Podolske, Eric J. Stith, Joseph Ryan Bennett, Gregory R. Carmichael, Arlindo da Silva, Ravi Govindaraju, Ruby Leung, Yang Zhang, Leonhard Pfister, Ju-Mee Ryoo, Jens Redemann, Robert Wood, and Paquita Zuidema
Atmos. Chem. Phys., 20, 11491–11526, https://doi.org/10.5194/acp-20-11491-2020, https://doi.org/10.5194/acp-20-11491-2020, 2020
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In the southeast Atlantic, well-defined smoke plumes from Africa advect over marine boundary layer cloud decks; both are most extensive around September, when most of the smoke resides in the free troposphere. A framework is put forth for evaluating the performance of a range of global and regional atmospheric composition models against observations made during the NASA ORACLES (ObseRvations of Aerosols above CLouds and their intEractionS) airborne mission in September 2016.
Zhenhao Ling, Qianqian Xie, Min Shao, Zhe Wang, Tao Wang, Hai Guo, and Xuemei Wang
Atmos. Chem. Phys., 20, 11451–11467, https://doi.org/10.5194/acp-20-11451-2020, https://doi.org/10.5194/acp-20-11451-2020, 2020
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The observation data from a receptor site in the Pearl River Delta region were analyzed by a photochemical box model with near-explicit chemical mechanisms (i.e., the Master Chemical Mechanism, MCM), improvements with reversible and irreversible heterogeneous processes of glyoxal and methylglyoxal, and the gas-particle partitioning of oxidation products in the present study.
Najin Kim, Seong Soo Yum, Minsu Park, Jong Sung Park, Hye Jung Shin, and Joon Young Ahn
Atmos. Chem. Phys., 20, 11245–11262, https://doi.org/10.5194/acp-20-11245-2020, https://doi.org/10.5194/acp-20-11245-2020, 2020
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Chemical effects on the size-resolved hygroscopicity of urban aerosols were examined based on the KORUS-AQ field campaign data (HTDMA and HR-ToF-AMS). The size-resolved chemical composition data were found to be critical in explaining the size-dependent hygroscopicity, as well as the diurnal variation of κ for small particles. Aerosol mixing state information was associated with the size-resolved chemical composition data to reveal chemical information of different hygroscopicity modes.
Liuwei Kong, Miao Feng, Yafei Liu, Yingying Zhang, Chen Zhang, Chenlu Li, Yu Qu, Junling An, Xingang Liu, Qinwen Tan, Nianliang Cheng, Yijun Deng, Ruixiao Zhai, and Zheng Wang
Atmos. Chem. Phys., 20, 11181–11199, https://doi.org/10.5194/acp-20-11181-2020, https://doi.org/10.5194/acp-20-11181-2020, 2020
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Secondary inorganic aerosols have an important contribution to PM2.5. Based on 3 years of atmospheric observation data, this study systematically analyzed the pollution levels and chemical conversion characteristics of nitrate, sulfate and ammonium in PM2.5 in Chengdu, southwest China, and analyzed the emission and regional transport characteristics of their gaseous precursors. This conclusion can provide an important reference for the current air pollution control.
Wei Yuan, Ru-Jin Huang, Lu Yang, Ting Wang, Jing Duan, Jie Guo, Haiyan Ni, Yang Chen, Qi Chen, Yongjie Li, Ulrike Dusek, Colin O'Dowd, and Thorsten Hoffmann
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2020-703, https://doi.org/10.5194/acp-2020-703, 2020
Revised manuscript accepted for ACP
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We characterized the seasonal variations of nitrated aromatic compounds (NACs) in composition, sources, and their light absorption contribution to brown carbon aerosol in Xi'an, northwest China. Our results show that secondary formation and vehicular emission were dominant sources in summer (~ 80 %), while biomass burning and coal combustion were major sources in winter (~ 75 %). Our results indicate that the composition and sources of NACs have profound impact on the light absorption of BrC.
Chunshui Lin, Darius Ceburnis, Wei Xu, Eimear Heffernan, Stig Hellebust, John Gallagher, Ru-Jin Huang, Colin O'Dowd, and Jurgita Ovadnevaite
Atmos. Chem. Phys., 20, 10513–10529, https://doi.org/10.5194/acp-20-10513-2020, https://doi.org/10.5194/acp-20-10513-2020, 2020
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Chemical composition and sources of submicron aerosols (PM1) were simultaneously investigated at a kerbside site in the Dublin city center and at a residential site in suburban Dublin (~5 km apart) during both a nonheating and a heating period in 2018. This study highlights the temporal and spatial variability of sources within the Dublin city center and the need for additional aerosol characterization studies to improve targeted mitigation solutions for a greater impact on urban air quality.
Wanyu Zhao, Hong Ren, Kimitaka Kawamura, Huiyun Du, Xueshun Chen, Siyao Yue, Qiaorong Xie, Lianfang Wei, Ping Li, Xin Zeng, Shaofei Kong, Yele Sun, Zifa Wang, and Pingqing Fu
Atmos. Chem. Phys., 20, 10331–10350, https://doi.org/10.5194/acp-20-10331-2020, https://doi.org/10.5194/acp-20-10331-2020, 2020
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Our observations provide detailed information on the abundance and vertical distribution of dicarboxylic acids, oxoacids and α-dicarbonyls in PM2.5 collected at three heights based on a 325 m meteorological tower in Beijing in summer. Our results demonstrate that organic acids at the ground surface are largely associated with local traffic emissions, while long-range atmospheric transport followed by photochemical ageing contributes more in the urban boundary layer than the ground surface.
Dong Chen, Yu Zhao, Jie Zhang, Huan Yu, and Xingna Yu
Atmos. Chem. Phys., 20, 10193–10210, https://doi.org/10.5194/acp-20-10193-2020, https://doi.org/10.5194/acp-20-10193-2020, 2020
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We studied the characteristics and sources of aerosol scattering for Nanjing. The method of aerosol scattering estimation was optimized based on field measurements, and the impacts of aerosol size and composition were quantified. To explore the reasons for the reduced visibility, source apportionment of aerosol scattering was conducted by pollution level. This work stressed the linkage between aerosols and visibility and improved the understanding of emissions and their role in air quality.
James Brean, David C. S. Beddows, Zongbo Shi, Brice Temime-Roussel, Nicolas Marchand, Xavier Querol, Andrés Alastuey, María Cruz Minguillón, and Roy M. Harrison
Atmos. Chem. Phys., 20, 10029–10045, https://doi.org/10.5194/acp-20-10029-2020, https://doi.org/10.5194/acp-20-10029-2020, 2020
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New particle formation is a key process influencing both local air quality and climatically active cloud condensation nuclei concentrations. This study has carried out fundamental measurements of nucleation processes in Barcelona, Spain, and concludes that a mechanism involving stabilisation of sulfuric acid clusters by low molecular weight amines is primarily responsible for new particle formation events.
Songyun Fan, Yuan Gao, Robert M. Sherrell, Shun Yu, and Kaixuan Bu
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2020-651, https://doi.org/10.5194/acp-2020-651, 2020
Revised manuscript accepted for ACP
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Aerosol sampling was carried out at Palmer Station in the west Antarctic Peninsula during the austral summer of 2016–2017. This study generated the new data on the concentrations and particle-size distributions of aerosol trace elements in the marine atmosphere over this region. Measurement data allowed estimating the dry deposition fluxes. The new results are critically important to understand the properties of aerosol particles and regional biogeochemical cycles.
Yee Ka Wong, X. H. Hilda Huang, Peter K. K. Louie, Alfred L. C. Yu, Damgy H. L. Chan, and Jian Zhen Yu
Atmos. Chem. Phys., 20, 9871–9882, https://doi.org/10.5194/acp-20-9871-2020, https://doi.org/10.5194/acp-20-9871-2020, 2020
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We present an approach to track separate contributions to PM2.5 by gasoline and diesel vehicles through a positive matrix factorization analysis of online monitoring data measurable by relatively inexpensive analytical instruments. They are PM2.5 organic and elemental carbon, C2–C9 volatile organic compounds, and nitrogen oxide concentrations. The method was demonstrated to be effective by applying monitoring data spanning 6 years (2011–2017) from a roadside environment in Hong Kong.
Tianzeng Chen, Jun Liu, Qingxin Ma, Biwu Chu, Peng Zhang, Jinzhu Ma, Yongchun Liu, Cheng Zhong, Pengfei Liu, Yafei Wang, Yujing Mu, and Hong He
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2020-792, https://doi.org/10.5194/acp-2020-792, 2020
Revised manuscript accepted for ACP
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Effects of photochemical aging on the formation and evolution of summertime secondary aerosol was systematically investigated in suburb of Beijing. Higher PM1 concentration accompanied longer photochemical age (ta). Sulfate and more-oxidized OOA formation were significantly sensitive to the increase of
ta, and their contribution were greatly enhanced at elevated ta levels. Our results suggested that photochemical aging process played a crucial role in the PM1 and O3 pollution in summertime.
Yibei Wan, Xiangpeng Huang, Bin Jiang, Binyu Kuang, Manfei Lin, Deming Xia, Yuhong Liao, Jingwen Chen, Jian Zhen Yu, and Huan Yu
Atmos. Chem. Phys., 20, 9821–9835, https://doi.org/10.5194/acp-20-9821-2020, https://doi.org/10.5194/acp-20-9821-2020, 2020
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Biogenic iodine emission from macroalgae and microalgae could initiate atmospheric new particle formation (NPF). But it is unknown if other species are needed to drive the growth of new iodine particles in the marine boundary layer. Unlike the deeper understanding of organic compounds driving continental NPF, little is known about the organics involved in coastal or open-ocean NPF. This article reveals a new group of important organic compounds involved in this process.
Yang Gao, Deqiang Zhang, Juntao Wang, Huiwang Gao, and Xiaohong Yao
Atmos. Chem. Phys., 20, 9665–9677, https://doi.org/10.5194/acp-20-9665-2020, https://doi.org/10.5194/acp-20-9665-2020, 2020
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Through the cruise campaign conducted over marginal seas in China, we found that the concentrations of condensation nuclei (Ncn) and cloud condensation nuclei (Nccn) were 1 order of magnitude larger than those in remote clear marine atmospheres, indicating overwhelming contributions from marine traffic emissions and long-range continental transport. Moreover, we derived regression equations used to estimate Ncn and Nccn from SO2 when the direct observations of Ncn and Nccn are not available.
Qing Yu, Jing Chen, Weihua Qin, Siming Cheng, Yuepeng Zhang, Yuewei Sun, Ke Xin, and Mushtaq Ahmad
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2020-726, https://doi.org/10.5194/acp-2020-726, 2020
Revised manuscript accepted for ACP
Yang Chen, Jing Cai, Zhichao Wang, Chao Peng, Xiaojiang Yao, Mi Tian, Yiqun Han, Guangming Shi, Zongbo Shi, Yue Liu, Xi Yang, Mei Zheng, Tong Zhu, Kebin He, Qiang Zhang, and Fumo Yang
Atmos. Chem. Phys., 20, 9231–9247, https://doi.org/10.5194/acp-20-9231-2020, https://doi.org/10.5194/acp-20-9231-2020, 2020
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Patterns of particle transport, accumulation, and evolution in both urban and rural areas of Beijing are investigated. The two sites shared 17 common particle types in different stages of atmospheric processing.
Yang Chen, Guangming Shi, Jing Cai, Zongbo Shi, Zhichao Wang, Xiaojiang Yao, Mi Tian, Chao Peng, Yiqun Han, Tong Zhu, Yue Liu, Xi Yang, Mei Zheng, Fumo Yang, Qiang Zhang, and Kebin He
Atmos. Chem. Phys., 20, 9249–9263, https://doi.org/10.5194/acp-20-9249-2020, https://doi.org/10.5194/acp-20-9249-2020, 2020
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Individual particles were observed in two field studies during winter 2016 in the urban and rural areas of Beijing. An online single-particle chemical composition analysis was used as a tracing system to investigate the impact of heating activities and the formation of haze events. During the pollution events, a pattern of transport and accumulation was found with evidence of single particles. The transport from Pinggu to Peking University was significant but PKU to PG occurred occasionally.
Stina Ausmeel, Axel Eriksson, Erik Ahlberg, Moa K. Sporre, Mårten Spanne, and Adam Kristensson
Atmos. Chem. Phys., 20, 9135–9151, https://doi.org/10.5194/acp-20-9135-2020, https://doi.org/10.5194/acp-20-9135-2020, 2020
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Emissions from shipping have an impact on air quality, especially in coastal areas. We have measured properties of the airborne particles in several plumes from ships that are sailing within an Emission Control Area. Individual ships showed large variability in contribution to total particle mass and nitrogen dioxide. Organics and sulfate dominated the particle mass, and most plumes contained very little or no soot. We also present recommendations for future stationary ship plume measurements.
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Our study presents an analysis of the vertical and horizontal black carbon properties across northern India using aircraft measurements. The Indo-Gangetic Plain saw the greatest black carbon mass concentrations during the pre-monsoon season. Two black carbon modes were recorded: a small black carbon mode (traffic emissions) in the north-west and a moderately coated mode (solid-fuel emissions) in the Indo-Gangetic Plain. In the vertical profile, absorption properties increase with height.
Our study presents an analysis of the vertical and horizontal black carbon properties across...
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