Articles | Volume 18, issue 21
https://doi.org/10.5194/acp-18-15601-2018
© Author(s) 2018. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/acp-18-15601-2018
© Author(s) 2018. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Research article
| 
30 Oct 2018
Research article |
| 30 Oct 2018
| 30 Oct 2018
Source apportionment of fine particulate matter in Houston, Texas: insights to secondary organic aerosols
Ibrahim M. Al-Naiema
Department of Chemistry, University of Iowa, Iowa City, IA 52242 USA
Anusha P. S. Hettiyadura
Department of Chemistry, University of Iowa, Iowa City, IA 52242 USA
Henry W. Wallace
Department of Civil and Environmental Engineering, Rice University,
Houston, TX 77005, USA
Nancy P. Sanchez
Department of Civil and Environmental Engineering, Rice University,
Houston, TX 77005, USA
Carter J. Madler
Department of Chemistry, University of Iowa, Iowa City, IA 52242 USA
Basak Karakurt Cevik
Department of Civil and Environmental Engineering, Rice University,
Houston, TX 77005, USA
Department of Energy Systems Engineering, Faculty of Engineering,
Yalova University, Yalova, 77100, Turkey
Alexander A. T. Bui
Department of Civil and Environmental Engineering, Rice University,
Houston, TX 77005, USA
Josh Kettler
Department of Chemistry, University of Iowa, Iowa City, IA 52242 USA
Robert J. Griffin
Department of Civil and Environmental Engineering, Rice University,
Houston, TX 77005, USA
Department of Chemical and Biomolecular Engineering, Rice University,
Houston, TX 77005, USA
Elizabeth A. Stone
CORRESPONDING AUTHOR
Department of Chemical and Biochemical Engineering, University of
Iowa, Iowa City, IA 52242, USA
Related authors
Anusha Priyadarshani Silva Hettiyadura, Ibrahim M. Al-Naiema, Dagen D. Hughes, Ting Fang, and Elizabeth A. Stone
Atmos. Chem. Phys., 19, 3191–3206, https://doi.org/10.5194/acp-19-3191-2019, https://doi.org/10.5194/acp-19-3191-2019, 2019
Short summary
Short summary
This study examines anthropogenic influences on secondary organic aerosol at an urban site in Atlanta, Georgia. Organosulfates accounted for 16.5 % of PM2.5 organic carbon and were mostly derived from isoprene. In contrast to a rural forested site, Atlanta's isoprene-derived organosulfate concentrations were 2–6 times higher and accounted for twice as much organic carbon. Insights are provided as to which organosulfates should be measured in future studies and targeted for standard development.
Ibrahim M. Al-Naiema and Elizabeth A. Stone
Atmos. Chem. Phys., 17, 2053–2065, https://doi.org/10.5194/acp-17-2053-2017, https://doi.org/10.5194/acp-17-2053-2017, 2017
Short summary
Short summary
Molecular tracers have proven useful in estimating contributions of primary and biogenic secondary sources to atmospheric particulate matter but have lagged behind for anthropogenic secondary sources. This study takes a field-based approach to evaluate the detectability, specificity, and gas–particle partitioning of prospective anthropogenic SOA tracers. We conclude that a subset of species are likely useful tracers and are recommended for use in future source apportionment studies.
Robert J. Yokelson, Bambang H. Saharjo, Chelsea E. Stockwell, Erianto I. Putra, Thilina Jayarathne, Acep Akbar, Israr Albar, Donald R. Blake, Laura L. B. Graham, Agus Kurniawan, Simone Meinardi, Diah Ningrum, Ati D. Nurhayati, Asmadi Saad, Niken Sakuntaladewi, Eko Setianto, Isobel J. Simpson, Elizabeth A. Stone, Sigit Sutikno, Andri Thomas, Kevin C. Ryan, and Mark A. Cochrane
Atmos. Chem. Phys., 22, 10173–10194, https://doi.org/10.5194/acp-22-10173-2022, https://doi.org/10.5194/acp-22-10173-2022, 2022
Short summary
Short summary
Fire plus non-fire GHG emissions associated with draining peatlands are the largest per area of any land use change considered by the IPCC. To characterize average and variability for tropical peat fire emissions, highly mobile smoke sampling teams were deployed across four Indonesian provinces to explore an extended interannual, climatic, and spatial range. Large adjustments to IPCC-recommended emissions are suggested. Lab data bolster an extensive emissions database for tropical peat fires.
Alexander A. T. Bui, Henry W. Wallace, Sarah Kavassalis, Hariprasad D. Alwe, James H. Flynn, Matt H. Erickson, Sergio Alvarez, Dylan B. Millet, Allison L. Steiner, and Robert J. Griffin
Atmos. Chem. Phys., 21, 17031–17050, https://doi.org/10.5194/acp-21-17031-2021, https://doi.org/10.5194/acp-21-17031-2021, 2021
Short summary
Short summary
Differences in atmospheric species above and below a forest canopy provide insight into the relative importance of local mixing, long-range transport, and chemical processes in determining vertical gradients in atmospheric particles in a forested environment. This helps in understanding the flux of climate-relevant material out of the forest to the atmosphere. We studied this in a remote forest using vertically resolved measurements of gases and particles.
Dandan Wei, Hariprasad D. Alwe, Dylan B. Millet, Brandon Bottorff, Michelle Lew, Philip S. Stevens, Joshua D. Shutter, Joshua L. Cox, Frank N. Keutsch, Qianwen Shi, Sarah C. Kavassalis, Jennifer G. Murphy, Krystal T. Vasquez, Hannah M. Allen, Eric Praske, John D. Crounse, Paul O. Wennberg, Paul B. Shepson, Alexander A. T. Bui, Henry W. Wallace, Robert J. Griffin, Nathaniel W. May, Megan Connor, Jonathan H. Slade, Kerri A. Pratt, Ezra C. Wood, Mathew Rollings, Benjamin L. Deming, Daniel C. Anderson, and Allison L. Steiner
Geosci. Model Dev., 14, 6309–6329, https://doi.org/10.5194/gmd-14-6309-2021, https://doi.org/10.5194/gmd-14-6309-2021, 2021
Short summary
Short summary
Over the past decade, understanding of isoprene oxidation has improved, and proper representation of isoprene oxidation and isoprene-derived SOA (iSOA) formation in canopy–chemistry models is now recognized to be important for an accurate understanding of forest–atmosphere exchange. The updated FORCAsT version 2.0 improves the estimation of some isoprene oxidation products and is one of the few canopy models currently capable of simulating SOA formation from monoterpenes and isoprene.
Blake Actkinson, Katherine Ensor, and Robert J. Griffin
Atmos. Meas. Tech., 14, 5809–5821, https://doi.org/10.5194/amt-14-5809-2021, https://doi.org/10.5194/amt-14-5809-2021, 2021
Short summary
Short summary
This paper describes the development of a new method used to estimate background from mobile monitoring time series. The method is tested on a previously published dataset, applied to an extensive mobile dataset, and compared with other previously published techniques used to estimate background. The results suggest that the method is a promising framework for background estimation.
Candice L. Sirmollo, Don R. Collins, Jordan M. McCormick, Cassandra F. Milan, Matthew H. Erickson, James H. Flynn, Rebecca J. Sheesley, Sascha Usenko, Henry W. Wallace, Alexander A. T. Bui, Robert J. Griffin, Matthew Tezak, Sean M. Kinahan, and Joshua L. Santarpia
Atmos. Meas. Tech., 14, 3351–3370, https://doi.org/10.5194/amt-14-3351-2021, https://doi.org/10.5194/amt-14-3351-2021, 2021
Short summary
Short summary
The newly developed portable 1 m3 CAGE chamber systems were characterized using data acquired during a 2-month field study in 2016 in a forested area north of Houston, TX, USA. Concentrations of several oxidant and organic compounds measured in the chamber were found to closely agree with those calculated with a zero-dimensional model. By tracking the modes of injected monodisperse particles, a pattern change was observed for hourly averaged growth rates between late summer and early fall.
Loredana G. Suciu, Robert J. Griffin, and Caroline A. Masiello
Geosci. Model Dev., 14, 907–921, https://doi.org/10.5194/gmd-14-907-2021, https://doi.org/10.5194/gmd-14-907-2021, 2021
Short summary
Short summary
Understanding the atmospheric degradation of biomass burning tracers such as levoglucosan is essential to decreasing uncertainties in the role of biomass burning in air quality, carbon cycling and paleoclimate. Using a 0-D modeling approach and numerical chamber simulations, we found that the multiphase atmospheric degradation of levoglucosan occurs over timescales of hours to days, can form secondary organic aerosols and affects other key tropospheric gases, such as ozone.
Md. Robiul Islam, Thilina Jayarathne, Isobel J. Simpson, Benjamin Werden, John Maben, Ashley Gilbert, Puppala S. Praveen, Sagar Adhikari, Arnico K. Panday, Maheswar Rupakheti, Donald R. Blake, Robert J. Yokelson, Peter F. DeCarlo, William C. Keene, and Elizabeth A. Stone
Atmos. Chem. Phys., 20, 2927–2951, https://doi.org/10.5194/acp-20-2927-2020, https://doi.org/10.5194/acp-20-2927-2020, 2020
Short summary
Short summary
The Kathmandu Valley experiences high levels of air pollution. In this study, atmospheric gases and particulate matter were characterized by online and off-line measurements, with an emphasis on understanding their sources. The major sources of particulate matter and trace gases were identified as garbage burning, biomass burning, and vehicles. The majority of secondary organic aerosol was attributed to anthropogenic precursors, while a minority was attributed to biogenic gases.
Qili Dai, Benjamin C. Schulze, Xiaohui Bi, Alexander A. T. Bui, Fangzhou Guo, Henry W. Wallace, Nancy P. Sanchez, James H. Flynn, Barry L. Lefer, Yinchang Feng, and Robert J. Griffin
Atmos. Chem. Phys., 19, 9641–9661, https://doi.org/10.5194/acp-19-9641-2019, https://doi.org/10.5194/acp-19-9641-2019, 2019
Short summary
Short summary
The formation processes of secondary organic aerosol remain to be fully understood. We reported the measurement data from two field campaigns within Houston, TX, to investigate the effects of aqueous-phase chemistry and photochemistry in processing oxygenated organic aerosol (OOA) in winter and summer. Both photochemistry and aqueous-phase processing appear to facilitate more-oxidized OOA formation. The processing mechanism of less-oxidized OOA apparently depended on relative humidity.
Min Zhong, Eri Saikawa, Alexander Avramov, Chen Chen, Boya Sun, Wenlu Ye, William C. Keene, Robert J. Yokelson, Thilina Jayarathne, Elizabeth A. Stone, Maheswar Rupakheti, and Arnico K. Panday
Atmos. Chem. Phys., 19, 8209–8228, https://doi.org/10.5194/acp-19-8209-2019, https://doi.org/10.5194/acp-19-8209-2019, 2019
Short summary
Short summary
Air pollution is one of the most pressing environmental issues in the Kathmandu Valley, the capital city of Nepal. We estimated emissions from two of the major source types in the valley (vehicles and brick kilns) and found that they have significant impacts on air quality surrounding the valley. Our results highlight the importance of improving local emissions estimates for air quality modeling.
Hansol D. Lee, Chathuri P. Kaluarachchi, Elias S. Hasenecz, Jonic Z. Zhu, Eduard Popa, Elizabeth A. Stone, and Alexei V. Tivanski
Atmos. Meas. Tech., 12, 2033–2042, https://doi.org/10.5194/amt-12-2033-2019, https://doi.org/10.5194/amt-12-2033-2019, 2019
Short summary
Short summary
Dry and wet aerosol deposition modes are commonly used to collect particles on a solid substrate for experiments. We demonstrate, using single-particle microscopy and bulk methods, how the substrate-deposited particles with two components can yield the same core–shell morphology but different shell thicknesses depending on the deposition method. Thus we strongly advise future works to use wet deposition when possible to obtain accurate assessment of the single-particle organic volume fraction.
Anusha Priyadarshani Silva Hettiyadura, Ibrahim M. Al-Naiema, Dagen D. Hughes, Ting Fang, and Elizabeth A. Stone
Atmos. Chem. Phys., 19, 3191–3206, https://doi.org/10.5194/acp-19-3191-2019, https://doi.org/10.5194/acp-19-3191-2019, 2019
Short summary
Short summary
This study examines anthropogenic influences on secondary organic aerosol at an urban site in Atlanta, Georgia. Organosulfates accounted for 16.5 % of PM2.5 organic carbon and were mostly derived from isoprene. In contrast to a rural forested site, Atlanta's isoprene-derived organosulfate concentrations were 2–6 times higher and accounted for twice as much organic carbon. Insights are provided as to which organosulfates should be measured in future studies and targeted for standard development.
J. Douglas Goetz, Michael R. Giordano, Chelsea E. Stockwell, Ted J. Christian, Rashmi Maharjan, Sagar Adhikari, Prakash V. Bhave, Puppala S. Praveen, Arnico K. Panday, Thilina Jayarathne, Elizabeth A. Stone, Robert J. Yokelson, and Peter F. DeCarlo
Atmos. Chem. Phys., 18, 14653–14679, https://doi.org/10.5194/acp-18-14653-2018, https://doi.org/10.5194/acp-18-14653-2018, 2018
Short summary
Short summary
Size distributions and emission factors of submicron aerosol were quantified using online techniques for a variety of common but under-sampled combustion sources in South Asia: wood and dung cooking fires, groundwater pumps, brick kilns, trash burning, and open burning of crop residues. Optical properties (brown carbon light absorption and the absorption Ångström exponent, AAE) of the emissions were also investigated. Contextual comparisons to the literature and other NAMaSTE results were made.
Benjamin C. Schulze, Henry W. Wallace, Alexander T. Bui, James H. Flynn, Matt H. Erickson, Sergio Alvarez, Qili Dai, Sascha Usenko, Rebecca J. Sheesley, and Robert J. Griffin
Atmos. Chem. Phys., 18, 14217–14241, https://doi.org/10.5194/acp-18-14217-2018, https://doi.org/10.5194/acp-18-14217-2018, 2018
Short summary
Short summary
Atmospheric field measurements at a coastal site near Houston, TX, were used to investigate the influence of shipping vessel emissions on aerosol mass and composition over the Gulf of Mexico. Results suggest that, despite recent regulations, these vessels still produce a considerable fraction of inorganic and organic aerosol mass in the region. Secondary effects of shipping emissions on organic aerosol composition, such as influences on aerosol aging, were also identified.
Thilina Jayarathne, Chelsea E. Stockwell, Ashley A. Gilbert, Kaitlyn Daugherty, Mark A. Cochrane, Kevin C. Ryan, Erianto I. Putra, Bambang H. Saharjo, Ati D. Nurhayati, Israr Albar, Robert J. Yokelson, and Elizabeth A. Stone
Atmos. Chem. Phys., 18, 2585–2600, https://doi.org/10.5194/acp-18-2585-2018, https://doi.org/10.5194/acp-18-2585-2018, 2018
Short summary
Short summary
Fine particulate matter (PM2.5) emissions from Indonesian peat burning were measured in situ. Fuel-based emission factors from 6.0–29.6 gPM kg-1. Detailed chemical analysis revealed high levels of organic carbon that was primarily water insoluble, little to no detectable elemental carbon, and alkane contributions to organic carbon in the range of 6 %. These data were used to estimate that 3.2–11 Tg of PM2.5 were emitted by the 2015 peat burning episodes in Indonesia.
Thilina Jayarathne, Chelsea E. Stockwell, Prakash V. Bhave, Puppala S. Praveen, Chathurika M. Rathnayake, Md. Robiul Islam, Arnico K. Panday, Sagar Adhikari, Rashmi Maharjan, J. Douglas Goetz, Peter F. DeCarlo, Eri Saikawa, Robert J. Yokelson, and Elizabeth A. Stone
Atmos. Chem. Phys., 18, 2259–2286, https://doi.org/10.5194/acp-18-2259-2018, https://doi.org/10.5194/acp-18-2259-2018, 2018
Short summary
Short summary
Emissions of fine particulate matter and its constituents were quantified for a variety of under-sampled combustion sources in South Asia: wood and dung cooking fires, generators, groundwater pumps, brick kilns, trash burning, and open burning of biomasses. Garbage burning and three-stone cooking fires were among the highest emitters, while servicing of motor vehicles significantly reduced PM. These data may be used in source apportionment and to update regional and global emission inventories.
Loredana G. Suciu, Robert J. Griffin, and Caroline A. Masiello
Atmos. Chem. Phys., 17, 6565–6581, https://doi.org/10.5194/acp-17-6565-2017, https://doi.org/10.5194/acp-17-6565-2017, 2017
Short summary
Short summary
Understanding of the variability of ozone (O3) in space and time is essential to the design of efficient air quality controls. We used statistical analysis of O3, nitrogen oxides (NOx) and weather measurements to estimate the large-scale contributions of O3 and NOx in southeastern Texas. We found that these “external” contributions have declined over time, likely due to a combination of controls on O3 precursors and increases in the frequency of prevailing southerly flow from the Gulf of Mexico.
Rudra P. Pokhrel, Eric R. Beamesderfer, Nick L. Wagner, Justin M. Langridge, Daniel A. Lack, Thilina Jayarathne, Elizabeth A. Stone, Chelsea E. Stockwell, Robert J. Yokelson, and Shane M. Murphy
Atmos. Chem. Phys., 17, 5063–5078, https://doi.org/10.5194/acp-17-5063-2017, https://doi.org/10.5194/acp-17-5063-2017, 2017
Short summary
Short summary
This study investigates enhancement of black carbon (BC) absorption in biomass burning emissions due to absorbing and non-absorbing coatings. The fraction of absorption due to BC, brown carbon (BrC), and lensing is estimated using different approaches. The similarities and differences between the results from these approaches are discussed. Absorption by BrC is shown to have good correlation with the elemental to organic carbon ratio (EC / OC) and AAE.
Chathurika M. Rathnayake, Nervana Metwali, Thilina Jayarathne, Josh Kettler, Yuefan Huang, Peter S. Thorne, Patrick T. O'Shaughnessy, and Elizabeth A. Stone
Atmos. Chem. Phys., 17, 2459–2475, https://doi.org/10.5194/acp-17-2459-2017, https://doi.org/10.5194/acp-17-2459-2017, 2017
Short summary
Short summary
Exposures to bioaerosols depend on their type, particle size, and concentration. While typically found in coarse particles (2.5–10 microns), pollens, fungal spores, and bacterial endotoxins decrease to less than 2.5 microns and simultaneously increase in concentration during rain events. These observations contrast the assumption that rain washes bioaerosols from the air and reduces allergen levels. Instead, population exposures to bioaerosols are expected to be enhanced during rain events.
Nga Lee Ng, Steven S. Brown, Alexander T. Archibald, Elliot Atlas, Ronald C. Cohen, John N. Crowley, Douglas A. Day, Neil M. Donahue, Juliane L. Fry, Hendrik Fuchs, Robert J. Griffin, Marcelo I. Guzman, Hartmut Herrmann, Alma Hodzic, Yoshiteru Iinuma, José L. Jimenez, Astrid Kiendler-Scharr, Ben H. Lee, Deborah J. Luecken, Jingqiu Mao, Robert McLaren, Anke Mutzel, Hans D. Osthoff, Bin Ouyang, Benedicte Picquet-Varrault, Ulrich Platt, Havala O. T. Pye, Yinon Rudich, Rebecca H. Schwantes, Manabu Shiraiwa, Jochen Stutz, Joel A. Thornton, Andreas Tilgner, Brent J. Williams, and Rahul A. Zaveri
Atmos. Chem. Phys., 17, 2103–2162, https://doi.org/10.5194/acp-17-2103-2017, https://doi.org/10.5194/acp-17-2103-2017, 2017
Short summary
Short summary
Oxidation of biogenic volatile organic compounds by NO3 is an important interaction between anthropogenic
and natural emissions. This review results from a June 2015 workshop and includes the recent literature
on kinetics, mechanisms, organic aerosol yields, and heterogeneous chemistry; advances in analytical
instrumentation; the current state NO3-BVOC chemistry in atmospheric models; and critical needs for
future research in modeling, field observations, and laboratory studies.
Ibrahim M. Al-Naiema and Elizabeth A. Stone
Atmos. Chem. Phys., 17, 2053–2065, https://doi.org/10.5194/acp-17-2053-2017, https://doi.org/10.5194/acp-17-2053-2017, 2017
Short summary
Short summary
Molecular tracers have proven useful in estimating contributions of primary and biogenic secondary sources to atmospheric particulate matter but have lagged behind for anthropogenic secondary sources. This study takes a field-based approach to evaluate the detectability, specificity, and gas–particle partitioning of prospective anthropogenic SOA tracers. We conclude that a subset of species are likely useful tracers and are recommended for use in future source apportionment studies.
Benjamin C. Schulze, Henry W. Wallace, James H. Flynn, Barry L. Lefer, Matt H. Erickson, B. Tom Jobson, Sebastien Dusanter, Stephen M. Griffith, Robert F. Hansen, Philip S. Stevens, Timothy VanReken, and Robert J. Griffin
Atmos. Chem. Phys., 17, 1805–1828, https://doi.org/10.5194/acp-17-1805-2017, https://doi.org/10.5194/acp-17-1805-2017, 2017
Short summary
Short summary
The atmospheric chemistry associated with mixing of anthropogenic and natural species was simulated to understand how shade provided by a forest canopy impacts reactions, product distribution, and subsequent phase distribution of the products. This is important to understand, as forested areas downwind of urban areas will be impacted by this phenomenon. It was found that fast transport from below the canopy led to increases in secondary organic aerosol from nitrate radicals above the canopy.
Anusha P. S. Hettiyadura, Thilina Jayarathne, Karsten Baumann, Allen H. Goldstein, Joost A. de Gouw, Abigail Koss, Frank N. Keutsch, Kate Skog, and Elizabeth A. Stone
Atmos. Chem. Phys., 17, 1343–1359, https://doi.org/10.5194/acp-17-1343-2017, https://doi.org/10.5194/acp-17-1343-2017, 2017
Short summary
Short summary
Organosulfates are components of secondary organic aerosol (SOA) formed in the presence of sulfate. Herein, their abundance, identity, and potential to form as sampling artifacts were studied in Centreville, AL, USA. The 10 most abundant signals accounted for 58–78 % of the total, with at least 20–200 other species accounting for the remainder. These major species were largely associated with biogenic gases, like isoprene and monoterpenes, and are proposed targets for future standard development.
Marie Ila Gosselin, Chathurika M. Rathnayake, Ian Crawford, Christopher Pöhlker, Janine Fröhlich-Nowoisky, Beatrice Schmer, Viviane R. Després, Guenter Engling, Martin Gallagher, Elizabeth Stone, Ulrich Pöschl, and J. Alex Huffman
Atmos. Chem. Phys., 16, 15165–15184, https://doi.org/10.5194/acp-16-15165-2016, https://doi.org/10.5194/acp-16-15165-2016, 2016
Short summary
Short summary
We present an analysis of bioaerosol measurements using two real-time fluorescence instruments in combination with molecular tracer techniques for quantifying airborne fungal spores in a semi-arid forest. Both techniques provide fungal spore concentrations of the order of 104 m−3 and up to 30 % of particle mass. Rainy periods exhibited higher concentrations and stronger correlations between fluorescent bioparticle and molecular tracer measurements. Fungal culture results are also presented.
Chelsea E. Stockwell, Thilina Jayarathne, Mark A. Cochrane, Kevin C. Ryan, Erianto I. Putra, Bambang H. Saharjo, Ati D. Nurhayati, Israr Albar, Donald R. Blake, Isobel J. Simpson, Elizabeth A. Stone, and Robert J. Yokelson
Atmos. Chem. Phys., 16, 11711–11732, https://doi.org/10.5194/acp-16-11711-2016, https://doi.org/10.5194/acp-16-11711-2016, 2016
Short summary
Short summary
We present the first or rare field measurements of emission factors for Indonesian peat fires made in Borneo during the 2015 El Niño. The data include up to 90 gases, aerosol mass, and aerosol optical properties at two wavelengths (405 and 870 nm). Brown carbon dominates aerosol absorption, revisions to previous values for greenhouse gas emissions are supported and air toxics are assessed.
Chelsea E. Stockwell, Ted J. Christian, J. Douglas Goetz, Thilina Jayarathne, Prakash V. Bhave, Puppala S. Praveen, Sagar Adhikari, Rashmi Maharjan, Peter F. DeCarlo, Elizabeth A. Stone, Eri Saikawa, Donald R. Blake, Isobel J. Simpson, Robert J. Yokelson, and Arnico K. Panday
Atmos. Chem. Phys., 16, 11043–11081, https://doi.org/10.5194/acp-16-11043-2016, https://doi.org/10.5194/acp-16-11043-2016, 2016
Short summary
Short summary
We present the first, or rare, field measurements in South Asia of emission factors for up to 80 gases (pollutants, greenhouse gases, and precursors) and black carbon and aerosol optical properties at 405 and 870 nm for many previously under-sampled sources that are important in developing countries such as cooking with dung and wood, garbage and crop residue burning, brick kilns, motorcycles, generators and pumps, etc. Brown carbon contributes significantly to total aerosol absorption.
Matthieu Riva, Thais Da Silva Barbosa, Ying-Hsuan Lin, Elizabeth A. Stone, Avram Gold, and Jason D. Surratt
Atmos. Chem. Phys., 16, 11001–11018, https://doi.org/10.5194/acp-16-11001-2016, https://doi.org/10.5194/acp-16-11001-2016, 2016
Short summary
Short summary
Formation of organosulfates (OSs) in secondary organic aerosol from the photooxidation of alkanes is reported from smog chamber experiments. Effects of acidity and relative humidity on OS formation were examined. Most of the OSs identified could be explained by formation of gaseous epoxide and/or hydroperoxide precursors with subsequent acid-catalyzed multiphase chemistry onto sulfate aerosol. The OSs identified here were also observed and quantified in aerosols collected in two urban areas.
Rudra P. Pokhrel, Nick L. Wagner, Justin M. Langridge, Daniel A. Lack, Thilina Jayarathne, Elizabeth A. Stone, Chelsea E. Stockwell, Robert J. Yokelson, and Shane M. Murphy
Atmos. Chem. Phys., 16, 9549–9561, https://doi.org/10.5194/acp-16-9549-2016, https://doi.org/10.5194/acp-16-9549-2016, 2016
Short summary
Short summary
This paper gives first multi-wavelength estimates of SSA and AAE of emissions from combustion of Indonesian peat. In addition, it demonstrates that SSA of biomass burning emissions can be parameterized with EC / (EC+OC) and that this parameterization is quantitatively superior to previously published parameterizations based on MCE. It also shows that EC / (EC+OC) parameterization accurately predicts SSA during the first few hours of aging of a biomass burning plume.
Matthew L. Dawson, Jialu Xu, Robert J. Griffin, and Donald Dabdub
Geosci. Model Dev., 9, 2143–2151, https://doi.org/10.5194/gmd-9-2143-2016, https://doi.org/10.5194/gmd-9-2143-2016, 2016
Short summary
Short summary
The atmospheric oxidation of aromatic compounds is an important source of aerosol-forming species, and thus contributes to pollution in urban areas. However, details of the mechanisms by which oxidation occurs are only recently being elucidated. Here we report the incorporation of a newly developed mechanism for aromatic oxidation into the UCI-CIT regional air quality model. Results suggest an unexpected role for chemical pathways typically associated with cleaner environments.
Weruka Rattanavaraha, Kevin Chu, Sri Hapsari Budisulistiorini, Matthieu Riva, Ying-Hsuan Lin, Eric S. Edgerton, Karsten Baumann, Stephanie L. Shaw, Hongyu Guo, Laura King, Rodney J. Weber, Miranda E. Neff, Elizabeth A. Stone, John H. Offenberg, Zhenfa Zhang, Avram Gold, and Jason D. Surratt
Atmos. Chem. Phys., 16, 4897–4914, https://doi.org/10.5194/acp-16-4897-2016, https://doi.org/10.5194/acp-16-4897-2016, 2016
Short summary
Short summary
The mechanisms by which specific anthropogenic pollutants enhance isoprene SOA in ambient PM2.5 remain unclear. As one aspect of an investigation to examine how anthropogenic pollutants influence isoprene-derived SOA formation, high-volume PM2.5 filter samples were collected from Birmingham, AL, during the 2013 Southern Oxidant and Aerosol Study (SOAS). Isoprene SOA tracers were measured from these samples and compared to gas and aerosol data collected from the SEARCH network.
Min Zhong, Eri Saikawa, Yang Liu, Vaishali Naik, Larry W. Horowitz, Masayuki Takigawa, Yu Zhao, Neng-Huei Lin, and Elizabeth A. Stone
Geosci. Model Dev., 9, 1201–1218, https://doi.org/10.5194/gmd-9-1201-2016, https://doi.org/10.5194/gmd-9-1201-2016, 2016
Short summary
Short summary
Large discrepancies exist among emission inventories (e.g., REAS and EDGAR) at the provincial level in China. We use WRF-Chem to evaluate the impact of the difference in existing emission inventories and find that emissions inputs significantly affect our air pollutant simulation results. Our study highlights the importance of constraining emissions at the provincial level for regional air quality modeling over East Asia.
E. W. Butt, A. Rap, A. Schmidt, C. E. Scott, K. J. Pringle, C. L. Reddington, N. A. D. Richards, M. T. Woodhouse, J. Ramirez-Villegas, H. Yang, V. Vakkari, E. A. Stone, M. Rupakheti, P. S. Praveen, P. G. van Zyl, J. P. Beukes, M. Josipovic, E. J. S. Mitchell, S. M. Sallu, P. M. Forster, and D. V. Spracklen
Atmos. Chem. Phys., 16, 873–905, https://doi.org/10.5194/acp-16-873-2016, https://doi.org/10.5194/acp-16-873-2016, 2016
Short summary
Short summary
We estimate the impact of residential emissions (cooking and heating) on atmospheric aerosol, human health, and climate. We find large contributions to annual mean ambient PM2.5 in residential sources regions resulting in significant but uncertain global premature mortality when key uncertainties in emission flux are considered. We show that residential emissions exert an uncertain global radiative effect and suggest more work is needed to characterise residential emissions climate importance.
K. Ashworth, S. H. Chung, R. J. Griffin, J. Chen, R. Forkel, A. M. Bryan, and A. L. Steiner
Geosci. Model Dev., 8, 3765–3784, https://doi.org/10.5194/gmd-8-3765-2015, https://doi.org/10.5194/gmd-8-3765-2015, 2015
Short summary
Short summary
Volatile organic compounds released from forests into the atmosphere play a key role in governing atmospheric concentrations of trace gases and aerosol particles. We describe the development of a 1-D model that simulates the processes occurring within and above the forest canopy that regulate the transfer of these compounds and their products. We evaluate model performance by comparison of modelled concentrations against measurements from a field campaign at a northern Michigan forest site.
S. H. Budisulistiorini, X. Li, S. T. Bairai, J. Renfro, Y. Liu, Y. J. Liu, K. A. McKinney, S. T. Martin, V. F. McNeill, H. O. T. Pye, A. Nenes, M. E. Neff, E. A. Stone, S. Mueller, C. Knote, S. L. Shaw, Z. Zhang, A. Gold, and J. D. Surratt
Atmos. Chem. Phys., 15, 8871–8888, https://doi.org/10.5194/acp-15-8871-2015, https://doi.org/10.5194/acp-15-8871-2015, 2015
Short summary
Short summary
Isoprene epoxydiols (IEPOX) are major gas-phase products from the atmospheric oxidation of isoprene that yield secondary organic aerosol (SOA) by reactive uptake onto acidic sulfate aerosol. We report a substantial contribution of IEPOX-derived SOA to the total fine aerosol collected during summer. IEPOX-derived SOA measured by online and offline mass spectrometry techniques is correlated with acidic sulfate aerosol, demonstrating the critical role of anthropogenic emissions in its formation.
A. P. S. Hettiyadura, E. A. Stone, S. Kundu, Z. Baker, E. Geddes, K. Richards, and T. Humphry
Atmos. Meas. Tech., 8, 2347–2358, https://doi.org/10.5194/amt-8-2347-2015, https://doi.org/10.5194/amt-8-2347-2015, 2015
Short summary
Short summary
Organosulfates are SOA products that have proven difficult to quantify. This study addresses the need for authentic quantification standards with a straightforward approach to synthesizing highly pure organosulfate potassium salts. New standards are used to develop a new separation protocol for small, functionalized organosulfates. Upon validation, this method is used to assess sample preparation protocols and to make new measurements of organosulfates in Centreville, Alabama.
S. Kundu, T. A. Quraishi, G. Yu, C. Suarez, F. N. Keutsch, and E. A. Stone
Atmos. Chem. Phys., 13, 4865–4875, https://doi.org/10.5194/acp-13-4865-2013, https://doi.org/10.5194/acp-13-4865-2013, 2013
Related subject area
Subject: Aerosols | Research Activity: Field Measurements | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Bridging gas and aerosol properties between the northeastern US and Bermuda: analysis of eight transit flights
The behaviour of charged particles (ions) during new particle formation events in urban Leipzig, Germany
Exploring the sources of light-absorbing carbonaceous aerosols by integrating observational and modeling results: insights from Northeast China
Measurement report: Characteristics of airborne black-carbon-containing particles during the 2021 summer COVID-19 lockdown in a typical Yangtze River Delta city, China
Aerosol optical properties within the atmospheric boundary layer predicted from ground-based observations compared to Raman lidar retrievals during RITA-2021
Hygroscopic growth and activation changed submicron aerosol composition and properties in the North China Plain
Measurement report: Formation of tropospheric brown carbon in a lifting air mass
Vertical variability of aerosol properties and trace gases over a remote marine region: a case study over Bermuda
Differences in aerosol and cloud properties along the central California coast when winds change from northerly to southerly
International airport emissions and their impact on local air quality: chemical speciation of ambient aerosols at Madrid–Barajas Airport during the AVIATOR campaign
The local ship speed reduction effect on black carbon emissions measured at a remote marine station
High-altitude aerosol chemical characterization and source identification: insights from the CALISHTO campaign
Measurement report: Impact of emission control measures on environmental persistent free radicals and reactive oxygen species – a short-term case study in Beijing
Characterizing water solubility of fresh and aged secondary organic aerosol in PM2.5 with the stable carbon isotope technique
Measurement report: Impact of cloud processes on secondary organic aerosols at a forested mountain site in southeastern China
Critical contribution of chemically diverse carbonyl molecules to the oxidative potential of atmospheric aerosols
Measurement report: Vanadium-containing ship exhaust particles detected in and above the marine boundary layer in the remote atmosphere
Diverging trends in aerosol sulfate and nitrate measured in the remote North Atlantic in Barbados are attributed to clean air policies, African smoke, and anthropogenic emissions
Diverse sources and aging change the mixing state and ice nucleation properties of aerosol particles over the western Pacific and Southern Ocean
The water-insoluble organic carbon in PM2.5 of typical Chinese urban areas: light-absorbing properties, potential sources, radiative forcing effects, and a possible light-absorbing continuum
Measurement report: Size-resolved secondary organic aerosol formation modulated by aerosol water uptake in wintertime haze
In situ measurement of organic aerosol molecular markers in urban Hong Kong during a summer period: temporal variations and source apportionment
Technical note: Determining chemical composition of atmospheric single particles by a standard-free mass calibration algorithm
Different formation pathways of nitrogen-containing organic compounds in aerosols and fog water in northern China
Automated compound speciation, cluster analysis, and quantification of organic vapours and aerosols using comprehensive two-dimensional gas chromatography and mass spectrometry
Atmospheric evolution of environmentally persistent free radicals in rural North China Plain: insights into water solubility and effects on PM2.5 oxidative potential
Impact of weather patterns and meteorological factors on PM2.5 and O3 responses to the COVID-19 lockdown in China
Daytime and nighttime aerosol soluble iron formation in clean and slightly polluted moist air in a coastal city in eastern China
Non-negligible secondary contribution to brown carbon in autumn and winter: inspiration from particulate nitrated and oxygenated aromatic compounds in urban Beijing
A Multi-site Passive Approach for Studying the Emissions and Evolution of Smoke from Prescribed Fires
Simultaneous organic aerosol source apportionment at two Antarctic sites reveals large-scale and ecoregion-specific components
Two distinct ship emission profiles for organic-sulfate source apportionment of PM in sulfur emission control areas
Measurement report: Optical characterization, seasonality, and sources of brown carbon in fine aerosols from Tianjin, North China: year-round observations
Bayesian inference-based estimation of hourly primary and secondary organic carbon in suburban Hong Kong: multi-temporal-scale variations and evolution characteristics during PM2.5 episodes
Primary and secondary emissions from a modern fleet of city buses
Dominant Influence of Biomass Combustion and Cross-Border Transport on Nitrogen-Containing Organic Compound Levels in the Southeastern Tibetan Plateau
Measurement report: Characteristics of aminiums in PM2.5 during winter clean and polluted episodes in China: aminium outbreak and its constraint
Impact assessment of terrestrial and marine air-mass on the constituents and intermixing of bioaerosols over coastal atmosphere
Assessing the influence of long-range transport of aerosols on the PM2.5 chemical composition and concentration in the Aburrá Valley
Measurement report: Characteristics of nitrogen-containing organics in PM2.5 in Ürümqi, northwestern China – differential impacts of combustion of fresh and aged biomass materials
Measurement report: Bio-physicochemistry of tropical clouds at Maïdo (Réunion, Indian Ocean): overview of results from the BIO-MAÏDO campaign
Impacts of elevated anthropogenic emissions on physicochemical characteristics of BC-containing particles over the Tibetan Plateau
Chemical properties and single-particle mixing state of soot aerosol in Houston during the TRACER campaign
Measurement report: Evaluation of the TOF-ACSM-CV for PM1.0 and PM2.5 measurements during the RITA-2021 field campaign
Sea salt reactivity over the northwest Atlantic: an in-depth look using the airborne ACTIVATE dataset
Measurement report: Atmospheric ice nuclei in the Changbai Mountains (2623 m a.s.l.) in northeastern Asia
Morphological and optical properties of carbonaceous aerosol particles from ship emissions and biomass burning during a summer cruise measurement in the South China Sea
Tropical tropospheric aerosol sources and chemical composition observed at high altitude in the Bolivian Andes
Chemical composition, sources and formation mechanism of urban PM2.5 in Southwest China: a case study at the beginning of 2023
Chemical characterization of atmospheric aerosols at a high-altitude mountain site: a study of source apportionment
Cassidy Soloff, Taiwo Ajayi, Yonghoon Choi, Ewan C. Crosbie, Joshua P. DiGangi, Glenn S. Diskin, Marta A. Fenn, Richard A. Ferrare, Francesca Gallo, Johnathan W. Hair, Miguel Ricardo A. Hilario, Simon Kirschler, Richard H. Moore, Taylor J. Shingler, Michael A. Shook, Kenneth L. Thornhill, Christiane Voigt, Edward L. Winstead, Luke D. Ziemba, and Armin Sorooshian
Atmos. Chem. Phys., 24, 10385–10408, https://doi.org/10.5194/acp-24-10385-2024, https://doi.org/10.5194/acp-24-10385-2024, 2024
Short summary
Short summary
Using aircraft measurements over the northwestern Atlantic between the US East Coast and Bermuda and trajectory modeling of continental outflow, we identify trace gas and particle properties that exhibit gradients with offshore distance and quantify these changes with high-resolution measurements of concentrations and particle chemistry, size, and scattering properties. This work furthers our understanding of the complex interactions between continental and marine environments.
Alex Rowell, James Brean, David C. S. Beddows, Zongbo Shi, Avinash Kumar, Matti Rissanen, Miikka Dal Maso, Peter Mettke, Kay Weinhold, Maik Merkel, and Roy M. Harrison
Atmos. Chem. Phys., 24, 10349–10361, https://doi.org/10.5194/acp-24-10349-2024, https://doi.org/10.5194/acp-24-10349-2024, 2024
Short summary
Short summary
Ions enhance the formation and growth rates of new particles, affecting the Earth's radiation budget. Despite these effects, there is little published data exploring the sources of ions in the urban environment and their role in new particle formation (NPF). Here we show that natural ion sources dominate in urban environments, while traffic is a secondary source. Ions contribute up to 12.7 % of the formation rate of particles, indicating that they are important for forming urban PM.
Yuan Cheng, Xu-bing Cao, Sheng-qiang Zhu, Zhi-qing Zhang, Jiu-meng Liu, Hong-liang Zhang, Qiang Zhang, and Ke-bin He
Atmos. Chem. Phys., 24, 9869–9883, https://doi.org/10.5194/acp-24-9869-2024, https://doi.org/10.5194/acp-24-9869-2024, 2024
Short summary
Short summary
The agreement between observational and modeling results is essential for the development of efficient air pollution control strategies. Here we constrained the modeling results of carbonaceous aerosols by field observation in Northeast China, a historically overlooked but recently targeted region of national clean-air actions. Our study suggested that the simulation of agricultural fire emissions and secondary organic aerosols remains challenging.
Yuan Dai, Junfeng Wang, Houjun Wang, Shijie Cui, Yunjiang Zhang, Haiwei Li, Yun Wu, Ming Wang, Eleonora Aruffo, and Xinlei Ge
Atmos. Chem. Phys., 24, 9733–9748, https://doi.org/10.5194/acp-24-9733-2024, https://doi.org/10.5194/acp-24-9733-2024, 2024
Short summary
Short summary
Short-term strict emission control can improve air quality, but its effectiveness needs assessment. During the 2021 summer COVID-19 lockdown in Yangzhou, we found that PM2.5 levels did not decrease despite reduced primary emissions. Aged black-carbon particles increased substantially due to higher O3 levels and transported pollutants. High humidity and low wind also played key roles. The results highlight the importance of a regionally balanced control strategy for future air quality management.
Xinya Liu, Diego Alves Gouveia, Bas Henzing, Arnoud Apituley, Arjan Hensen, Danielle van Dinther, Rujin Huang, and Ulrike Dusek
Atmos. Chem. Phys., 24, 9597–9614, https://doi.org/10.5194/acp-24-9597-2024, https://doi.org/10.5194/acp-24-9597-2024, 2024
Short summary
Short summary
The vertical distribution of aerosol optical properties is important for their effect on climate. This is usually measured by lidar, which has limitations, most notably the assumption of a lidar ratio. Our study shows that routine surface-level aerosol measurements are able to predict this lidar ratio reasonably well within the lower layers of the atmosphere and thus provide a relatively simple and cost-effective method to improve lidar measurements.
Weiqi Xu, Ye Kuang, Wanyun Xu, Zhiqiang Zhang, Biao Luo, Xiaoyi Zhang, Jiangchuang Tao, Hongqin Qiao, Li Liu, and Yele Sun
Atmos. Chem. Phys., 24, 9387–9399, https://doi.org/10.5194/acp-24-9387-2024, https://doi.org/10.5194/acp-24-9387-2024, 2024
Short summary
Short summary
We deployed an advanced aerosol–fog sampling system at a rural site in the North China Plain to investigate impacts of aerosol hygroscopic growth and activation on the physicochemical properties of submicron aerosols. Observed results highlighted remarkably different aqueous processing of primary and secondary submicron aerosol components under distinct ambient relative humidity (RH) conditions and that RH levels significantly impact aerosol sampling through the aerosol swelling effect.
Can Wu, Xiaodi Liu, Ke Zhang, Si Zhang, Cong Cao, Jianjun Li, Rui Li, Fan Zhang, and Gehui Wang
Atmos. Chem. Phys., 24, 9263–9275, https://doi.org/10.5194/acp-24-9263-2024, https://doi.org/10.5194/acp-24-9263-2024, 2024
Short summary
Short summary
Brown carbon (BrC) is prevalent in the troposphere and can efficiently absorb solar and terrestrial radiation. Our observations show that the enhanced light absorption of BrC relative to black carbon at the tropopause can be attributed to the formation of nitrogen-containing organic compounds through the aqueous-phase reactions of carbonyls with ammonium.
Taiwo Ajayi, Yonghoon Choi, Ewan C. Crosbie, Joshua P. DiGangi, Glenn S. Diskin, Marta A. Fenn, Richard A. Ferrare, Johnathan W. Hair, Miguel Ricardo A. Hilario, Chris A. Hostetler, Simon Kirschler, Richard H. Moore, Taylor J. Shingler, Michael A. Shook, Cassidy Soloff, Kenneth L. Thornhill, Christiane Voigt, Edward L. Winstead, Luke D. Ziemba, and Armin Sorooshian
Atmos. Chem. Phys., 24, 9197–9218, https://doi.org/10.5194/acp-24-9197-2024, https://doi.org/10.5194/acp-24-9197-2024, 2024
Short summary
Short summary
This study uses airborne data to examine vertical profiles of trace gases, aerosol particles, and meteorological variables over a remote marine area (Bermuda). Results show distinct differences based on both air mass source region (North America, Ocean, Caribbean/North Africa) and altitude for a given air mass type. This work highlights the sensitivity of remote marine areas to long-range transport and the importance of considering the vertical dependence of trace gas and aerosol properties.
Kira Zeider, Grace Betito, Anthony Bucholtz, Peng Xian, Annette Walker, and Armin Sorooshian
Atmos. Chem. Phys., 24, 9059–9083, https://doi.org/10.5194/acp-24-9059-2024, https://doi.org/10.5194/acp-24-9059-2024, 2024
Short summary
Short summary
The predominant wind direction along the California coast (northerly) reverses several times during the summer (to southerly). The effects of these wind reversals on aerosol and cloud characteristics are not well understood. Using data from multiple datasets we found that southerly flow periods had enhanced signatures of anthropogenic emissions due to shipping and continental sources, and clouds had more but smaller droplets.
Saleh Alzahrani, Doğuşhan Kılıç, Michael Flynn, Paul I. Williams, and James Allan
Atmos. Chem. Phys., 24, 9045–9058, https://doi.org/10.5194/acp-24-9045-2024, https://doi.org/10.5194/acp-24-9045-2024, 2024
Short summary
Short summary
This paper investigates emissions from aviation activities at an international airport to evaluate their impact on local air quality. The study provides detailed insights into the chemical composition of aerosols and key pollutants in the airport environment. Source apportionment analysis using positive matrix factorisation (PMF) identified three significant sources: less oxidised oxygenated organic aerosol, alkane organic aerosol, and more oxidised oxygenated organic aerosol.
Mikko Heikkilä, Krista Luoma, Timo Mäkelä, and Tiia Grönholm
Atmos. Chem. Phys., 24, 8927–8941, https://doi.org/10.5194/acp-24-8927-2024, https://doi.org/10.5194/acp-24-8927-2024, 2024
Short summary
Short summary
Black carbon (BC) concentration was measured from 211 ship exhaust gas plumes at a remote marine station. Emission factors of BC were calculated in grams per kilogram of fuel. Ships with an exhaust gas cleaning system (EGCS) were found to have median BC emissions per fuel consumed 5 times lower than ships without an EGCS. However, this might be because of non-EGCS ships running at low engine loads rather than the EGCS itself. A local speed restriction would increase BC emissions of ships.
Olga Zografou, Maria Gini, Prodromos Fetfatzis, Konstantinos Granakis, Romanos Foskinis, Manousos Ioannis Manousakas, Fotios Tsopelas, Evangelia Diapouli, Eleni Dovrou, Christina N. Vasilakopoulou, Alexandros Papayannis, Spyros N. Pandis, Athanasios Nenes, and Konstantinos Eleftheriadis
Atmos. Chem. Phys., 24, 8911–8926, https://doi.org/10.5194/acp-24-8911-2024, https://doi.org/10.5194/acp-24-8911-2024, 2024
Short summary
Short summary
Characterization of PM1 and positive matrix factorization (PMF) source apportionment of organic and inorganic fractions were conducted at the high-altitude station (HAC)2. Cloud presence reduced PM1, affecting sulfate more than organics. Free-troposphere (FT) conditions showed more black carbon (eBC) than planetary boundary layer (PBL) conditions.
Yuanyuan Qin, Xinghua Zhang, Wei Huang, Juanjuan Qin, Xiaoyu Hu, Yuxuan Cao, Tianyi Zhao, Yang Zhang, Jihua Tan, Ziyin Zhang, Xinming Wang, and Zhenzhen Wang
Atmos. Chem. Phys., 24, 8737–8750, https://doi.org/10.5194/acp-24-8737-2024, https://doi.org/10.5194/acp-24-8737-2024, 2024
Short summary
Short summary
Environmental persistent free radicals (EPFRs) and reactive oxygen species (ROSs) play an active role in the atmosphere. Despite control measures having effectively reduced their emissions, reductions were less than in PM2.5. Emission control measures performed well in achieving Parade Blue, but reducing the impact of the atmosphere on human health remains challenging. Thus, there is a need to reassess emission control measures to better address the challenges posed by EPFRs and ROSs.
Fenghua Wei, Xing Peng, Liming Cao, Mengxue Tang, Ning Feng, Xiaofeng Huang, and Lingyan He
Atmos. Chem. Phys., 24, 8507–8518, https://doi.org/10.5194/acp-24-8507-2024, https://doi.org/10.5194/acp-24-8507-2024, 2024
Short summary
Short summary
The water solubility of secondary organic aerosols (SOAs) is a crucial factor in determining their hygroscopicity and climatic impact. Stable carbon isotope and mass spectrometry techniques were combined to assess the water solubility of SOAs with different aging degrees in a coastal megacity in China. This work revealed a much higher water-soluble fraction of aged SOA compared to fresh SOA, indicating that the aging degree of SOA has considerable impacts on its water solubility.
Zijun Zhang, Weiqi Xu, Yi Zhang, Wei Zhou, Xiangyu Xu, Aodong Du, Yinzhou Zhang, Hongqin Qiao, Ye Kuang, Xiaole Pan, Zifa Wang, Xueling Cheng, Lanzhong Liu, Qingyan Fu, Douglas R. Worsnop, Jie Li, and Yele Sun
Atmos. Chem. Phys., 24, 8473–8488, https://doi.org/10.5194/acp-24-8473-2024, https://doi.org/10.5194/acp-24-8473-2024, 2024
Short summary
Short summary
We investigated aerosol composition and sources and the interaction between secondary organic aerosol (SOA) and clouds at a regional mountain site in southeastern China. Clouds efficiently scavenge more oxidized SOA; however, cloud evaporation leads to the production of less oxidized SOA. The unexpectedly high presence of nitrate in aerosol particles indicates that nitrate formed in polluted areas has undergone interactions with clouds, significantly influencing the regional background site.
Feifei Li, Shanshan Tang, Jitao Lv, Shiyang Yu, Xu Sun, Dong Cao, Yawei Wang, and Guibin Jiang
Atmos. Chem. Phys., 24, 8397–8411, https://doi.org/10.5194/acp-24-8397-2024, https://doi.org/10.5194/acp-24-8397-2024, 2024
Short summary
Short summary
Targeted derivatization and non-targeted analysis with Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) were used to reveal the molecular composition of carbonyl molecules in PM2.5, and the important role of carbonyls in increasing the oxidative potential of organic aerosol was found in real samples.
Maya Abou-Ghanem, Daniel M. Murphy, Gregory P. Schill, Michael J. Lawler, and Karl D. Froyd
Atmos. Chem. Phys., 24, 8263–8275, https://doi.org/10.5194/acp-24-8263-2024, https://doi.org/10.5194/acp-24-8263-2024, 2024
Short summary
Short summary
Using particle analysis by laser mass spectrometry, we examine vanadium-containing ship exhaust particles measured on NASA's DC-8 during the Atmospheric Tomography Mission (ATom). Our results reveal ship exhaust particles are sufficiently widespread in the marine atmosphere and experience atmospheric aging. Finally, we use laboratory calibrations to determine the vanadium, sulfate, and organic single-particle mass fractions of vanadium-containing ship exhaust particles.
Cassandra J. Gaston, Joseph M. Prospero, Kristen Foley, Havala O. T. Pye, Lillian Custals, Edmund Blades, Peter Sealy, and James A. Christie
Atmos. Chem. Phys., 24, 8049–8066, https://doi.org/10.5194/acp-24-8049-2024, https://doi.org/10.5194/acp-24-8049-2024, 2024
Short summary
Short summary
To understand how changing emissions have impacted aerosols in remote regions, we measured nitrate and sulfate in Barbados and compared them to model predictions from EPA’s Air QUAlity TimE Series (EQUATES). Nitrate was stable, except for spikes in 2008 and 2010 due to transported smoke. Sulfate decreased in the 1990s due to reductions in sulfur dioxide (SO2) in the US and Europe; then it increased in the 2000s, likely due to anthropogenic emissions from Africa.
Jiao Xue, Tian Zhang, Keyhong Park, Jinpei Yan, Young Jun Yoon, Jiyeon Park, and Bingbing Wang
Atmos. Chem. Phys., 24, 7731–7754, https://doi.org/10.5194/acp-24-7731-2024, https://doi.org/10.5194/acp-24-7731-2024, 2024
Short summary
Short summary
Ice formation by particles is an important way of making mixed-phase and ice clouds. We found that particles collected in the marine atmosphere exhibit diverse ice nucleation abilities and mixing states. Sea salt mixed-sulfate particles were enriched in ice-nucleating particles. Selective aging on sea salt particles made particle populations more externally mixed. Characterizations of particles and their mixing state are needed for a better understanding of aerosol–cloud interactions.
Yangzhi Mo, Jun Li, Guangcai Zhong, Sanyuan Zhu, Shizhen Zhao, Jiao Tang, Hongxing Jiang, Zhineng Cheng, Chongguo Tian, Yingjun Chen, and Gan Zhang
Atmos. Chem. Phys., 24, 7755–7772, https://doi.org/10.5194/acp-24-7755-2024, https://doi.org/10.5194/acp-24-7755-2024, 2024
Short summary
Short summary
In this study, we found that biomass burning (31.0 %) and coal combustion (31.1 %) were the dominant sources of water-insoluble organic carbon in China, with coal combustion sources exhibiting the strongest light-absorbing capacity. Additionally, we propose a light-absorbing carbonaceous continuum, revealing that components enriched with fossil sources tend to have stronger light-absorbing capacity, higher aromaticity, higher molecular weights, and greater recalcitrance in the atmosphere.
Jing Duan, Ru-Jin Huang, Ying Wang, Wei Xu, Haobin Zhong, Chunshui Lin, Wei Huang, Yifang Gu, Jurgita Ovadnevaite, Darius Ceburnis, and Colin O'Dowd
Atmos. Chem. Phys., 24, 7687–7698, https://doi.org/10.5194/acp-24-7687-2024, https://doi.org/10.5194/acp-24-7687-2024, 2024
Short summary
Short summary
The chemical composition of atmospheric particles has shown significant changes in recent years. We investigated the potential effects of changes in inorganics on aerosol water uptake and, thus, secondary organic aerosol formation in wintertime haze based on the size-resolved measurements of non-refractory fine particulate matter (NR-PM2.5) in Xi’an, northwestern China. We highlight the key role of aerosol water as a medium to link inorganics and organics in their multiphase processes.
Hongyong Li, Xiaopu Lyu, Likun Xue, Yunxi Huo, Dawen Yao, Haoxian Lu, and Hai Guo
Atmos. Chem. Phys., 24, 7085–7100, https://doi.org/10.5194/acp-24-7085-2024, https://doi.org/10.5194/acp-24-7085-2024, 2024
Short summary
Short summary
Organic aerosol is ubiquitous in the atmosphere and largely explains the gap between current levels of fine particulate matter in many cities and the World Health Organization guideline values. This study highlights the dominant contributions of cooking emissions to organic aerosol when marine air prevailed in Hong Kong, which were occasionally overwhelmed by aromatics-derived secondary organic aerosol in continental ouflows.
Shao Shi, Jinghao Zhai, Xin Yang, Yechun Ruan, Yuanlong Huang, Xujian Chen, Antai Zhang, Jianhuai Ye, Guomao Zheng, Baohua Cai, Yaling Zeng, Yixiang Wang, Chunbo Xing, Yujie Zhang, Tzung-May Fu, Lei Zhu, Huizhong Shen, and Chen Wang
Atmos. Chem. Phys., 24, 7001–7012, https://doi.org/10.5194/acp-24-7001-2024, https://doi.org/10.5194/acp-24-7001-2024, 2024
Short summary
Short summary
The determination of ions in the mass spectra of individual particles remains uncertain. We have developed a standard-free mass calibration algorithm applicable to more than 98 % of ambient particles. With our algorithm, ions with ~ 0.05 Th mass difference could be determined. Therefore, many more atmospheric species could be determined and involved in the source apportionment of aerosols, the study of chemical reaction mechanisms, and the analysis of single-particle mixing states.
Wei Sun, Xiaodong Hu, Yuzhen Fu, Guohua Zhang, Yujiao Zhu, Xinfeng Wang, Caiqing Yan, Likun Xue, He Meng, Bin Jiang, Yuhong Liao, Xinming Wang, Ping'an Peng, and Xinhui Bi
Atmos. Chem. Phys., 24, 6987–6999, https://doi.org/10.5194/acp-24-6987-2024, https://doi.org/10.5194/acp-24-6987-2024, 2024
Short summary
Short summary
The formation pathways of nitrogen-containing compounds (NOCs) in the atmosphere remain unclear. We investigated the composition of aerosols and fog water by state-of-the-art mass spectrometry and compared the formation pathways of NOCs. We found that NOCs in aerosols were mainly formed through nitration reaction, while ammonia addition played a more important role in fog water. The results deepen our understanding of the processes of organic particulate pollution.
Xiao He, Xuan Zheng, Shuwen Guo, Lewei Zeng, Ting Chen, Bohan Yang, Shupei Xiao, Qiongqiong Wang, Zhiyuan Li, Yan You, Shaojun Zhang, and Ye Wu
EGUsphere, https://doi.org/10.5194/egusphere-2024-1671, https://doi.org/10.5194/egusphere-2024-1671, 2024
Short summary
Short summary
This study introduces an innovative method for identifying and quantifying complex organic vapors and aerosols. By combining advanced analytical techniques and new algorithms, we categorized thousands of compounds from heavy-duty diesel vehicles and ambient air and highlighted specific tracers for emission sources. The innovative approach enhances peak identification, reduces quantification uncertainties, and offers new insights for air quality management and atmospheric chemistry.
Xu Yang, Fobang Liu, Shuqi Yang, Yuling Yang, Yanan Wang, Jingjing Li, Mingyu Zhao, Zhao Wang, Kai Wang, Chi He, and Haijie Tong
EGUsphere, https://doi.org/10.5194/egusphere-2024-1622, https://doi.org/10.5194/egusphere-2024-1622, 2024
Short summary
Short summary
A study in rural North China Plain revealed Environmental persistent free radicals (EPFRs) in atmospheric particulate matter (PM), with a notable water-soluble fraction likely from atmospheric oxidation during transport. Significant positive correlations between EPFRs and the water-soluble oxidative potential of PM2.5 were found, primarily attributable to the water-soluble fractions of EPFRs. These findings emphasize understanding EPFRs’ atmospheric evolution for climate and health impacts.
Fuzhen Shen, Michaela I. Hegglin, and Yue Yuan
Atmos. Chem. Phys., 24, 6539–6553, https://doi.org/10.5194/acp-24-6539-2024, https://doi.org/10.5194/acp-24-6539-2024, 2024
Short summary
Short summary
We attempt to use a novel structural self-organising map and machine learning models to identify a weather system and quantify the importance of each meteorological factor in driving the unexpected PM2.5 and O3 changes under the specific weather system during the COVID-19 lockdown in China. The result highlights that temperature under the double-centre high-pressure system plays the most crucial role in abnormal events.
Wenshuai Li, Yuxuan Qi, Yingchen Liu, Guanru Wu, Yanjing Zhang, Jinhui Shi, Wenjun Qu, Lifang Sheng, Wencai Wang, Daizhou Zhang, and Yang Zhou
Atmos. Chem. Phys., 24, 6495–6508, https://doi.org/10.5194/acp-24-6495-2024, https://doi.org/10.5194/acp-24-6495-2024, 2024
Short summary
Short summary
Aerosol particles from mainland can transport to oceans and deposit, providing soluble Fe and affecting phytoplankton growth. Thus, we studied the dissolution process of aerosol Fe and found that photochemistry played a key role in promoting Fe dissolution in clean conditions. RH-dependent reactions were more influential in slightly polluted conditions. These results highlight the distinct roles of two weather-related parameters (radiation and RH) in influencing geochemical cycles related to Fe.
Yanqin Ren, Zhenhai Wu, Yuanyuan Ji, Fang Bi, Junling Li, Haijie Zhang, Hao Zhang, Hong Li, and Gehui Wang
Atmos. Chem. Phys., 24, 6525–6538, https://doi.org/10.5194/acp-24-6525-2024, https://doi.org/10.5194/acp-24-6525-2024, 2024
Short summary
Short summary
Nitrated aromatic compounds (NACs) and oxygenated derivatives of polycyclic aromatic hydrocarbons (OPAHs) in PM2.5 were examined from an urban area in Beijing during the autumn and winter. The OPAH and NAC concentrations were much higher during heating than before heating. They majorly originated from the combustion of biomass and automobile emissions, and the secondary generation was the major contributor throughout the whole sampling period.
Rime El Asmar, Zongrun Li, David J. Tanner, Yongtao Hu, Susan O’Neill, L. Gregory Huey, M. Talat Odman, and Rodney J. Weber
EGUsphere, https://doi.org/10.5194/egusphere-2024-1485, https://doi.org/10.5194/egusphere-2024-1485, 2024
Short summary
Short summary
Prescribed burning is an important method for managing ecosystems and preventing wildfires, however, smoke from prescribed fires can have a significant impact on air quality. Here, using a network of fixed sites and sampling throughout an extended prescribed burning period in two different years, we characterize the emissions and evolution up to 8 hours of PM2.5 mass, BC, and BrC in smoke from burning of forested lands in the southeastern US.
Marco Paglione, David C. S. Beddows, Anna Jones, Thomas Lachlan-Cope, Matteo Rinaldi, Stefano Decesari, Francesco Manarini, Mara Russo, Karam Mansour, Roy M. Harrison, Andrea Mazzanti, Emilio Tagliavini, and Manuel Dall'Osto
Atmos. Chem. Phys., 24, 6305–6322, https://doi.org/10.5194/acp-24-6305-2024, https://doi.org/10.5194/acp-24-6305-2024, 2024
Short summary
Short summary
Applying factor analysis techniques to H-NMR spectra, we present the organic aerosol (OA) source apportionment of PM1 samples collected in parallel at two Antarctic stations, namely Signy and Halley, allowing investigation of aerosol–climate interactions in an unperturbed atmosphere. Our results show remarkable differences between pelagic (open-ocean) and sympagic (sea-ice-influenced) air masses and indicate that various sources and processes are controlling Antarctic aerosols.
Kirsten N. Fossum, Chunshui Lin, Niall O'Sullivan, Lu Lei, Stig Hellebust, Darius Ceburnis, Aqeel Afzal, Anja Tremper, David Green, Srishti Jain, Steigvilė Byčenkienė, Colin O'Dowd, John Wenger, and Jurgita Ovadnevaite
EGUsphere, https://doi.org/10.5194/egusphere-2024-1262, https://doi.org/10.5194/egusphere-2024-1262, 2024
Short summary
Short summary
The chemical composition and sources of submicron aerosol in the Dublin Port area were investigated over a month-long campaign. Two distinct types of ship emissions were identified and characterized: sulfate-rich plumes from use of heavy fuel oil with scrubbers and organic-rich plumes from use of low sulfur fuels. The latter were more frequent, emitting double the particle number, and having atypical V/Ni ratio for ship emission.
Zhichao Dong, Chandra Mouli Pavuluri, Peisen Li, Zhanjie Xu, Junjun Deng, Xueyan Zhao, Xiaomai Zhao, Pingqing Fu, and Cong-Qiang Liu
Atmos. Chem. Phys., 24, 5887–5905, https://doi.org/10.5194/acp-24-5887-2024, https://doi.org/10.5194/acp-24-5887-2024, 2024
Short summary
Short summary
Comprehensive study of optical properties of brown carbon (BrC) in fine aerosols from Tianjin, China, implied that biological emissions are major sources of BrC in summer, whereas fossil fuel combustion and biomass burning emissions are in cold periods. The direct radiation absorption caused by BrC in short wavelengths contributed about 40 % to that caused by BrC in 300–700 nm. Water-insoluble but methanol-soluble BrC contains more protein-like chromophores (PLOM) than that of water-soluble BrC.
Shan Wang, Kezheng Liao, Zijing Zhang, Yuk Ying Cheng, Qiongqiong Wang, Hanzhe Chen, and Jian Zhen Yu
Atmos. Chem. Phys., 24, 5803–5821, https://doi.org/10.5194/acp-24-5803-2024, https://doi.org/10.5194/acp-24-5803-2024, 2024
Short summary
Short summary
In this work, hourly primary and secondary organic carbon were estimated by a novel Bayesian inference approach in suburban Hong Kong. Their multi-temporal-scale variations and evolution characteristics during PM2.5 episodes were examined. The methodology could serve as a guide for other locations with similar monitoring capabilities. The observation-based results are helpful for understanding the evolving nature of secondary organic aerosols and refining the accuracy of model simulations.
Liyuan Zhou, Qianyun Liu, Christian M. Salvador, Michael Le Breton, Mattias Hallquist, Jian Zhen Yu, Chak K. Chan, and Åsa M. Hallquist
EGUsphere, https://doi.org/10.5194/egusphere-2024-494, https://doi.org/10.5194/egusphere-2024-494, 2024
Short summary
Short summary
Our research on city bus emissions reveals that alternative fuels (compressed natural gas and biofuels) reduce fresh particle emissions compared to diesel. However, all fuels lead to secondary air pollution. Aiming at guiding better environmental policies, we studied 76 buses using advanced emission measurement techniques. This work sheds light on the complex effects of bus fuels on urban air quality, emphasizing the need for comprehensive evaluations of future transportation technologies.
Meng Wang, Qiyuan Wang, Steven Sai Hang Ho, Jie Tian, Yong Zhang, Shun-cheng Lee, and Junji Cao
EGUsphere, https://doi.org/10.5194/egusphere-2024-1130, https://doi.org/10.5194/egusphere-2024-1130, 2024
Short summary
Short summary
This study explores nitrogen-containing organic compounds (NOCs) in PM2.5 particles on the Southeastern Tibetan Plateau. We discovered that biomass burning and transboundary transport are the primary sources of NOCs in the high-altitude area. Understanding these aerosol sources informs how they contribute to regional and potentially global climate changes. Our findings could help shape effective environmental policies to enhance air quality and address climate impacts in this sensitive region.
Yu Xu, Tang Liu, Yi-Jia Ma, Qi-Bin Sun, Hong-Wei Xiao, Hao Xiao, and Hua-Yun Xiao
EGUsphere, https://doi.org/10.5194/egusphere-2024-975, https://doi.org/10.5194/egusphere-2024-975, 2024
Short summary
Short summary
This study has explored the characteristics of aminiums, ammonium, and PM2.5 from the clean days to the polluted days according to the observational data from 11 different Chinese cities, highlighting the possibility of the competitive uptake of ammonia versus amines on acidic aerosols, or the displacement of aminiums by ammonia under a high ammonia condition. The overall results deepen the understanding of the spatiotemporal differences in aminium characteristic and formation in China.
Qun He, Zhaowen Wang, Houfeng Liu, Pengju Xu, Rongbao Duan, Caihong Xu, Jianmin Chen, and Min Wei
EGUsphere, https://doi.org/10.5194/egusphere-2024-841, https://doi.org/10.5194/egusphere-2024-841, 2024
Short summary
Short summary
Coastal environments provide an ideal setting for investigating the intermixing processes of terrestrial and marine aerosols. Terrestrial air mass constituted a larger proportion during severe air pollution, harboring more animal and human pathogens. A relative shift towards marine air-mass with respect to pollution elimination, where saprophytic bacteria and fungi were predominant. Mixed air-mass reveals the intermixing processes of terrestrial and marine sources.
Maria P. Velásquez-García, K. Santiago Hernández, James A. Vergara-Correa, Richard J. Pope, Miriam Gómez-Marín, and Angela M. Rendón
EGUsphere, https://doi.org/10.5194/egusphere-2024-695, https://doi.org/10.5194/egusphere-2024-695, 2024
Short summary
Short summary
For the Aburrá Valley, Colombia, local emissions dominate aerosol concentrations, which degrade air quality (AQ) and impact human health. However, this can be exacerbated by the influx of external emissions from sources such as regional fires, Saharan dust, and volcanic degassing. While substantially increasing city-wide aerosols, these external sources can also degrade the aerosol chemical composition (i.e. their toxicity) and impact AQ, which we investigate in this study.
Yi-Jia Ma, Yu Xu, Ting Yang, Hong-Wei Xiao, and Hua-Yun Xiao
Atmos. Chem. Phys., 24, 4331–4346, https://doi.org/10.5194/acp-24-4331-2024, https://doi.org/10.5194/acp-24-4331-2024, 2024
Short summary
Short summary
This study provides field-based evidence about the differential impacts of combustion of fresh and aged biomass materials on aerosol nitrogen-containing organic compounds (NOCs) in different seasons in Ürümqi, bridging the linkages between the observations and previous laboratory studies showing the formation mechanisms of NOCs.
Maud Leriche, Pierre Tulet, Laurent Deguillaume, Frédéric Burnet, Aurélie Colomb, Agnès Borbon, Corinne Jambert, Valentin Duflot, Stéphan Houdier, Jean-Luc Jaffrezo, Mickaël Vaïtilingom, Pamela Dominutti, Manon Rocco, Camille Mouchel-Vallon, Samira El Gdachi, Maxence Brissy, Maroua Fathalli, Nicolas Maury, Bert Verreyken, Crist Amelynck, Niels Schoon, Valérie Gros, Jean-Marc Pichon, Mickael Ribeiro, Eric Pique, Emmanuel Leclerc, Thierry Bourrianne, Axel Roy, Eric Moulin, Joël Barrie, Jean-Marc Metzger, Guillaume Péris, Christian Guadagno, Chatrapatty Bhugwant, Jean-Mathieu Tibere, Arnaud Tournigand, Evelyn Freney, Karine Sellegri, Anne-Marie Delort, Pierre Amato, Muriel Joly, Jean-Luc Baray, Pascal Renard, Angelica Bianco, Anne Réchou, and Guillaume Payen
Atmos. Chem. Phys., 24, 4129–4155, https://doi.org/10.5194/acp-24-4129-2024, https://doi.org/10.5194/acp-24-4129-2024, 2024
Short summary
Short summary
Aerosol particles in the atmosphere play a key role in climate change and air pollution. A large number of aerosol particles are formed from the oxidation of volatile organic compounds (VOCs and secondary organic aerosols – SOA). An important field campaign was organized on Réunion in March–April 2019 to understand the formation of SOA in a tropical atmosphere mostly influenced by VOCs emitted by forest and in the presence of clouds. This work synthesizes the results of this campaign.
Jinbo Wang, Jiaping Wang, Yuxuan Zhang, Tengyu Liu, Xuguang Chi, Xin Huang, Dafeng Ge, Shiyi Lai, Caijun Zhu, Lei Wang, Qiaozhi Zha, Ximeng Qi, Wei Nie, Congbin Fu, and Aijun Ding
EGUsphere, https://doi.org/10.5194/egusphere-2024-879, https://doi.org/10.5194/egusphere-2024-879, 2024
Short summary
Short summary
In this study, we found large spatial discrepancies in the physical and chemical properties of black carbon over the Tibetan Plateau (TP). Elevated anthropogenic emissions from low-altitude regions can significantly change the mass concentration, mixing state and chemical composition of black carbon -containing aerosol in TP region, further altering its light absorption ability. Our study emphasizes the vulnerability of remote plateau regions to intense anthropogenic influences.
Ryan N. Farley, James E. Lee, Laura-Hélèna Rivellini, Alex K. Y. Lee, Rachael Dal Porto, Christopher D. Cappa, Kyle Gorkowski, Abu Sayeed Md Shawon, Katherine B. Benedict, Allison C. Aiken, Manvendra K. Dubey, and Qi Zhang
Atmos. Chem. Phys., 24, 3953–3971, https://doi.org/10.5194/acp-24-3953-2024, https://doi.org/10.5194/acp-24-3953-2024, 2024
Short summary
Short summary
The black carbon aerosol composition and mixing state were characterized using a soot particle aerosol mass spectrometer. Single-particle measurements revealed the major role of atmospheric processing in modulating the black carbon mixing state. A significant fraction of soot particles were internally mixed with oxidized organic aerosol and sulfate, with implications for activation as cloud nuclei.
Xinya Liu, Bas Henzing, Arjan Hensen, Jan Mulder, Peng Yao, Danielle van Dinther, Jerry van Bronckhorst, Rujin Huang, and Ulrike Dusek
Atmos. Chem. Phys., 24, 3405–3420, https://doi.org/10.5194/acp-24-3405-2024, https://doi.org/10.5194/acp-24-3405-2024, 2024
Short summary
Short summary
We evaluated the time-of-flight aerosol chemical speciation monitor (TOF-ACSM) following the implementation of the PM2.5 aerodynamic lens and a capture vaporizer (CV). The results showed that it significantly improved the accuracy and precision of ACSM in the field observations. The paper elucidates the measurement outcomes of various instruments and provides an analysis of their biases. This comprehensive evaluation is expected to benefit the ACSM community and other aerosol field measurements.
Eva-Lou Edwards, Yonghoon Choi, Ewan C. Crosbie, Joshua P. DiGangi, Glenn S. Diskin, Claire E. Robinson, Michael A. Shook, Edward L. Winstead, Luke D. Ziemba, and Armin Sorooshian
Atmos. Chem. Phys., 24, 3349–3378, https://doi.org/10.5194/acp-24-3349-2024, https://doi.org/10.5194/acp-24-3349-2024, 2024
Short summary
Short summary
We investigate Cl− depletion in sea salt particles over the northwest Atlantic from December 2021 to June 2022 using an airborne dataset. Losses of Cl− are greatest in May and least in December–February and March. Inorganic acidic species can account for all depletion observed for December–February, March, and June near Bermuda but none in May. Quantifying Cl− depletion as a percentage captures seasonal trends in depletion but fails to convey the effects it may have on atmospheric oxidation.
Yue Sun, Yujiao Zhu, Yanbin Qi, Lanxiadi Chen, Jiangshan Mu, Ye Shan, Yu Yang, Yanqiu Nie, Ping Liu, Can Cui, Ji Zhang, Mingxuan Liu, Lingli Zhang, Yufei Wang, Xinfeng Wang, Mingjin Tang, Wenxing Wang, and Likun Xue
Atmos. Chem. Phys., 24, 3241–3256, https://doi.org/10.5194/acp-24-3241-2024, https://doi.org/10.5194/acp-24-3241-2024, 2024
Short summary
Short summary
Field observations were conducted at the summit of Changbai Mountain in northeast Asia. The cumulative number concentration of ice-nucleating particles (INPs) varied from 1.6 × 10−3 to 78.3 L−1 over the temperature range of −5.5 to −29.0 ℃. Biological INPs (bio-INPs) accounted for the majority of INPs, and the proportion exceeded 90% above −13.0 ℃. Planetary boundary layer height, valley breezes, and long-distance transport of air mass influence the abundance of bio-INPs.
Cuizhi Sun, Yongyun Zhang, Baoling Liang, Min Gao, Xi Sun, Fei Li, Xue Ni, Qibin Sun, Hengjia Ou, Dexian Chen, Shengzhen Zhou, and Jun Zhao
Atmos. Chem. Phys., 24, 3043–3063, https://doi.org/10.5194/acp-24-3043-2024, https://doi.org/10.5194/acp-24-3043-2024, 2024
Short summary
Short summary
In a May–June 2021 expedition in the South China Sea, we analyzed black and brown carbon in marine aerosols, key to light absorption and climate impact. Using advanced in situ and microscope techniques, we observed particle size, structure, and tar balls mixed with various elements. Results showed biomass burning and fossil fuels majorly influence light absorption, especially during significant burning events. This research aids the understanding of carbonaceous aerosols' role in marine climate.
C. Isabel Moreno, Radovan Krejci, Jean-Luc Jaffrezo, Gaëlle Uzu, Andrés Alastuey, Marcos F. Andrade, Valeria Mardóñez, Alkuin Maximilian Koenig, Diego Aliaga, Claudia Mohr, Laura Ticona, Fernando Velarde, Luis Blacutt, Ricardo Forno, David N. Whiteman, Alfred Wiedensohler, Patrick Ginot, and Paolo Laj
Atmos. Chem. Phys., 24, 2837–2860, https://doi.org/10.5194/acp-24-2837-2024, https://doi.org/10.5194/acp-24-2837-2024, 2024
Short summary
Short summary
Aerosol chemical composition (ions, sugars, carbonaceous matter) from 2011 to 2020 was studied at Mt. Chacaltaya (5380 m a.s.l., Bolivian Andes). Minimum concentrations occur in the rainy season with maxima in the dry and transition seasons. The origins of the aerosol are located in a radius of hundreds of kilometers: nearby urban and rural areas, natural biogenic emissions, vegetation burning from Amazonia and Chaco, Pacific Ocean emissions, soil dust, and Peruvian volcanism.
Junke Zhang, Yunfei Su, Chunying Chen, Wenkai Guo, Qinwen Tan, Miao Feng, Danlin Song, Tao Jiang, Qiang Chen, Yuan Li, Wei Li, Yizhi Wang, Xiaojuan Huang, Lin Han, Wanqing Wu, and Gehui Wang
Atmos. Chem. Phys., 24, 2803–2820, https://doi.org/10.5194/acp-24-2803-2024, https://doi.org/10.5194/acp-24-2803-2024, 2024
Short summary
Short summary
Typical haze events in Chengdu at the beginning of 2023 were investigated with bulk-chemical and single-particle analyses along with numerical model simulations. By integrating the obtained chemical composition, source, mixing state and numerical simulation results, we infer that Haze-1 was mainly caused by pollutants related to fossil fuel combustion, especially local mobile sources, while Haze-2 was triggered by the secondary pollutants, which mainly came from regional transmission.
Elena Barbaro, Matteo Feltracco, Fabrizio De Blasi, Clara Turetta, Marta Radaelli, Warren Cairns, Giulio Cozzi, Giovanna Mazzi, Marco Casula, Jacopo Gabrieli, Carlo Barbante, and Andrea Gambaro
Atmos. Chem. Phys., 24, 2821–2835, https://doi.org/10.5194/acp-24-2821-2024, https://doi.org/10.5194/acp-24-2821-2024, 2024
Short summary
Short summary
The study analyzed a year of atmospheric aerosol composition at Col Margherita in the Italian Alps. Over 100 chemical markers were identified, including major ions, organic compounds, and trace elements. It revealed sources of aerosol, highlighted impacts of Saharan dust events, and showed anthropogenic pollution's influence despite the site's remoteness. Enrichment factors emphasized non-natural sources of trace elements. Source apportionment identified four key factors affecting the area.
Cited articles
Agrawal, H., Welch, W. A., Henningsen, S., Miller, J. W., and Cocker, D. R.:
Emissions from main propulsion engine on container ship at sea, J. Geophys.
Res., 115, D23205, https://doi.org/10.1029/2009jd013346, 2010.
Aiken, A. C., DeCarlo, P. F., Kroll, J. H., Worsnop, D. R., Huffman, J. A.,
Docherty, K. S., Ulbrich, I. M., Mohr, C., Kimmel, J. R., Sueper, D., Sun,
Y., Zhang, Q., Trimborn, A., Northway, M., Ziemann, P. J., Canagaratna, M.
R., Onasch, T. B., Alfarra, M. R., Prevot, A. S. H., Dommen, J., Duplissy,
J., Metzger, A., Baltensperger, U., and Jimenez, J. L.: O/C and OM/OC ratios
of primary, secondary, and ambient organic aerosols with high-resolution
time-of-flight aerosol mass spectrometry, Environ. Sci. Technol., 42,
4478–4485, https://doi.org/10.1021/es703009q, 2008.
Aiken, A. C., Salcedo, D., Cubison, M. J., Huffman, J. A., DeCarlo, P. F., Ulbrich, I. M.,
Docherty, K. S., Sueper, D., Kimmel, J. R., Worsnop, D. R., Trimborn, A., Northway, M., Stone,
E. A., Schauer, J. J., Volkamer, R. M., Fortner, E., de Foy, B., Wang, J., Laskin, A.,
Shutthanandan, V., Zheng, J., Zhang, R., Gaffney, J., Marley, N. A., Paredes-Miranda, G.,
Arnott, W. P., Molina, L. T., Sosa, G., and Jimenez, J. L.: Mexico City aerosol analysis
during MILAGRO using high resolution aerosol mass spectrometry at the urban supersite (T0) – Part 1:
Fine particle composition and organic source apportionment, Atmos. Chem. Phys., 9, 6633–6653,
https://doi.org/10.5194/acp-9-6633-2009, 2009.
Al-Naiema, I. M. and Stone, E. A.: Evaluation of anthropogenic secondary organic aerosol
tracers from aromatic hydrocarbons, Atmos. Chem. Phys., 17, 2053–2065,
https://doi.org/10.5194/acp-17-2053-2017, 2017.
Al-Naiema, I. M., Hettiyadura, A. P. S., Wallace, H. W., Sanchez, N. P.,
Madler, C. J., Cevik, B. K., Bui, A. A. T., Kettler, J., and Griffin, R. J.:
Replication data for: Source apportionment of fine particulate matter in
Houston, Texas: Insights to secondary organic aerosols,
https://doi.org/10.7910/DVN/NVMC5P, 2018.
Ayers, G. P., Keywood, M. D., and Gras, J. L.: TEOM vs. manual gravimetric
methods for determination of PM2.5 aerosol mass concentrations, Atmos.
Environ., 33, 3717–3721, https://doi.org/10.1016/S1352-2310(99)00125-9, 1999.
Belis, C. A., Karagulian, F., Larsen, B. R., and Hopke, P. K.: Critical
review and meta-analysis of ambient particulate matter source apportionment
using receptor models in Europe, Atmos. Environ., 69, 94–108,
https://doi.org/10.1016/j.atmosenv.2012.11.009, 2013.
Brown, S. S., Dubé, W. P., Bahreini, R., Middlebrook, A. M., Brock, C. A.,
Warneke, C., de Gouw, J. A., Washenfelder, R. A., Atlas, E., Peischl, J., Ryerson,
T. B., Holloway, J. S., Schwarz, J. P., Spackman, R., Trainer, M., Parrish, D. D.,
Fehshenfeld, F. C., and Ravishankara, A. R.: Biogenic VOC oxidation and organic
aerosol formation in an urban nocturnal boundary layer: aircraft vertical profiles
in Houston, TX, Atmos. Chem. Phys., 13, 11317–11337, https://doi.org/10.5194/acp-13-11317-2013, 2013.
Brown, S. G., Eberly, S., Paatero, P., and Norris, G. A.: Methods for
estimating uncertainty in PMF solutions: Examples with ambient air and water
quality data and guidance on reporting PMF results, Sci. Total Environ.,
518–519, 626–635, https://doi.org/10.1016/j.scitotenv.2015.01.022, 2015.
Budisulistiorini, S. H., Li, X., Bairai, S. T., Renfro, J., Liu, Y., Liu, Y. J.,
McKinney, K. A., Martin, S. T., McNeill, V. F., Pye, H. O. T., Nenes, A., Neff,
M. E., Stone, E. A., Mueller, S., Knote, C., Shaw, S. L., Zhang, Z., Gold, A.,
and Surratt, J. D.: Examining the effects of anthropogenic emissions on
isoprene-derived secondary organic aerosol formation during the 2013
Southern Oxidant and Aerosol Study (SOAS) at the Look Rock, Tennessee
ground site, Atmos. Chem. Phys., 15, 8871–8888, https://doi.org/10.5194/acp-15-8871-2015, 2015.
Buzcu, B., and Fraser, M. P.: Source identification and apportionment of
volatile organic compounds in Houston, TX, Atmos. Environ., 40, 2385–2400,
https://doi.org/10.1016/j.atmosenv.2005.12.020, 2006.
Buzcu, B., Yue, Z., Fraser, M., Nopmongcol, U., and Allen, D.: Secondary
particle formation and evidence of heterogeneous chemistry during a wood
smoke episode in Texas, J. Geophys. Res., 111, D10S13,
https://doi.org/10.1029/2005JD006143, 2006.
Cao, J. J., Lee, S. C., Ho, K. F., Zou, S. C., Fung, K., Li, Y., Watson, J.
G., and Chow, J. C.: Spatial and seasonal variations of atmospheric organic
carbon and elemental carbon in Pearl River Delta Region, China, Atmos.
Environ., 38, 4447–4456, https://doi.org/10.1016/j.atmosenv.2004.05.016, 2004.
Cao, L.-M., Huang, X.-F., Li, Y.-Y., Hu, M., and He, L.-Y.: Volatility
measurement of atmospheric submicron aerosols in an urban atmosphere in
southern China, Atmos. Chem. Phys., 18, 1729–1743, https://doi.org/10.5194/acp-18-1729-2018,
2018.
Chan, A. W. H., Kautzman, K. E., Chhabra, P. S., Surratt, J. D., Chan, M. N., Crounse, J. D.,
Kürten, A., Wennberg, P. O., Flagan, R. C., and Seinfeld, J. H.: Secondary organic aerosol
formation from photooxidation of naphthalene and alkylnaphthalenes: implications for
oxidation of intermediate volatility organic compounds (IVOCs), Atmos. Chem. Phys.,
9, 3049–3060, https://doi.org/10.5194/acp-9-3049-2009, 2009.
Christoffersen, T., Hjorth, J., Horie, O., Jensen, N., Kotzias, D.,
Molander, L., Neeb, P., Ruppert, L., Winterhalter, R., and Virkkula, A.:
cis-Pinic acid, a possible precursor for organic aerosol formation from
ozonolysis of α-pinene, Atmos. Environ., 32, 1657–1661,
https://doi.org/10.1016/S1352-2310(97)00448-2, 1998.
Cleveland, M. J., Ziemba, L. D., Griffin, R. J., Dibb, J. E., Anderson, C.
H., Lefer, B., and Rappengluck, B.: Characterization of urban aerosol using
aerosol mass spectrometry and proton nuclear magnetic resonance
spectroscopy, Atmos. Environ., 54, 511–518, https://doi.org/10.1016/j.atmosenv.2012.02.074,
2012.
Crounse, J. D., DeCarlo, P. F., Blake, D. R., Emmons, L. K., Campos, T. L.,
Apel, E. C., Clarke, A. D., Weinheimer, A. J., McCabe, D. C., Yokelson, R. J.,
Jimenez, J. L., and Wennberg, P. O.: Biomass burning and urban air pollution over
the Central Mexican Plateau, Atmos. Chem. Phys., 9, 4929–4944,
https://doi.org/10.5194/acp-9-4929-2009, 2009.
DeCarlo, P. F., Kimmel, J. R., Trimborn, A., Northway, M. J., Jayne, J. T.,
Aiken, A. C., Gonin, M., Fuhrer, K., Horvath, T., and Docherty, K. S.:
Field-deployable, high-resolution, time-of-flight aerosol mass spectrometer,
Anal. Chem., 78, 8281–8289, https://doi.org/10.1021/ac061249n, 2006.
Dechapanya, W., Russell, M., and Allen, D. T.: Estimates of anthropogenic
secondary organic aerosol formation in Houston, Texas, Aerosol Sci.
Technol., 38, 156–166, https://doi.org/10.1080/02786820390229462, 2004.
Docherty, K. S., Aiken, A. C., Huffman, J. A., Ulbrich, I. M., DeCarlo, P. F.,
Sueper, D., Worsnop, D. R., Snyder, D. C., Peltier, R. E., Weber, R. J., Grover,
B. D., Eatough, D. J., Williams, B. J., Goldstein, A. H., Ziemann, P. J., and
Jimenez, J. L.: The 2005 Study of Organic Aerosols at Riverside (SOAR-1):
instrumental intercomparisons and fine particle composition, Atmos. Chem. Phys., 11, 12387–12420,
https://doi.org/10.5194/acp-11-12387-2011, 2011.
Donahue, N. M., Robinson, A. L., Stanier, C. O., and Pandis, S. N.: Coupled
partitioning, dilution, and chemical aging of semivolatile organics,
Environ. Sci. Technol., 40, 2635–2643, 10.1021/es052297c, 2006.
Duncan, B. N., Martin, R. V., Staudt, A. C., Yevich, R., and Logan, J. A.:
Interannual and seasonal variability of biomass burning emissions
constrained by satellite observations, J. Geophys. Res., 108, 1–22, https://doi.org/10.1029/2002JD002378, 2003.
Elser, M., Huang, R.-J., Wolf, R., Slowik, J. G., Wang, Q., Canonaco, F., Li, G.,
Bozzetti, C., Daellenbach, K. R., Huang, Y., Zhang, R., Li, Z., Cao, J., Baltensperger,
U., El-Haddad, I., and Prévôt, A. S. H.: New insights into PM2.5 chemical composition
and sources in two major cities in China during extreme haze events using aerosol mass
spectrometry, Atmos. Chem. Phys., 16, 3207–3225, https://doi.org/10.5194/acp-16-3207-2016, 2016.
EPA-PMF: Positive matrix factorization (PMF) 5.0 Fundamentals and User Guide,
available at:
https://www.epa.gov/sites/production/files/2015-02/documents/pmf_5.0_user_guide.pdf
(last access: 10 October 2018), 2014.
Foley, K. M., Roselle, S. J., Appel, K. W., Bhave, P. V., Pleim, J. E., Otte, T. L., M
athur, R., Sarwar, G., Young, J. O., Gilliam, R. C., Nolte, C. G., Kelly, J. T., Gilliland,
A. B., and Bash, J. O.: Incremental testing of the Community Multiscale Air Quality (CMAQ)
modeling system version 4.7, Geosci. Model Dev., 3, 205–226, https://doi.org/10.5194/gmd-3-205-2010, 2010.
Forstner, H. J. L., Flagan, R. C., and Seinfeld, J. H.: Secondary organic
aerosol from the photooxidation of aromatic hydrocarbons: Molecular
composition, Environ. Sci. Technol., 31, 1345–1358, https://doi.org/10.1021/es9605376, 1997.
Fraser, M. P., Yue, Z. W., Tropp, R. J., Kohl, S. D., and Chow, J. C.:
Molecular composition of organic fine particulate matter in Houston, TX,
Atmos. Environ., 36, 5751–5758, https://doi.org/10.1016/S1352-2310(02)00725-2, 2002.
Fraser, M. P., Yue, Z. W., and Buzcu, B.: Source apportionment of fine
particulate matter in Houston, TX, using organic molecular markers, Atmos.
Environ., 37, 2117–2123, https://doi.org/10.1016/s1352-2310(03)00075-x, 2003.
Friese, E. and Ebel, A.: Temperature dependent dhermodynamic model of the
system
H+-NH4+-Na+-
Gentner, D. R., Isaacman, G., Worton, D. R., Chan, A. W., Dallmann, T. R.,
Davis, L., Liu, S., Day, D. A., Russell, L. M., and Wilson, K. R.:
Elucidating secondary organic aerosol from diesel and gasoline vehicles
through detailed characterization of organic carbon emissions, P. Natl. Acad.
Sci. USA, 109, 18318–18323, https://doi.org/10.1073/pnas.1212272109, 2012.
Goldstein, A. H. and Galbally, I. E.: Known and unexplored organic
constituents in the earth's atmosphere, Environ. Sci. Technol., 41,
1514–1521, https://doi.org/10.1021/es072476p, 2007.
Guo, H., Xu, L., Bougiatioti, A., Cerully, K. M., Capps, S. L., Hite Jr., J. R.,
Carlton, A. G., Lee, S.-H., Bergin, M. H., Ng, N. L., Nenes, A., and Weber, R. J.:
Fine-particle water and pH in the southeastern United States, Atmos. Chem. Phys.,
15, 5211–5228, https://doi.org/10.5194/acp-15-5211-2015, 2015.
Hallquist, M., Wenger, J. C., Baltensperger, U., Rudich, Y., Simpson, D., Claeys, M.,
Dommen, J., Donahue, N. M., George, C., Goldstein, A. H., Hamilton, J. F., Herrmann, H.,
Hoffmann, T., Iinuma, Y., Jang, M., Jenkin, M. E., Jimenez, J. L., Kiendler-Scharr, A.,
Maenhaut, W., McFiggans, G., Mentel, Th. F., Monod, A., Prévôt, A. S. H., Seinfeld, J. H.,
Surratt, J. D., Szmigielski, R., and Wildt, J.: The formation, properties and impact of
secondary organic aerosol: current and emerging issues, Atmos. Chem. Phys., 9, 5155–5236,
https://doi.org/10.5194/acp-9-5155-2009, 2009.
Harrison, M. A. J., Barra, S., Borghesi, D., Vione, D., Arsene, C., and
Olariu, R. L.: Nitrated phenols in the atmosphere: a review, Atmos.
Environ., 39, 231–248, https://doi.org/10.1016/j.atmosenv.2004.09.044, 2005.
Hennigan, C. J., Izumi, J., Sullivan, A. P., Weber, R. J., and Nenes, A.: A critical
evaluation of proxy methods used to estimate the acidity of atmospheric particles, Atmos.
Chem. Phys., 15, 2775–2790, https://doi.org/10.5194/acp-15-2775-2015, 2015.
Henze, D. K., Seinfeld, J. H., Ng, N. L., Kroll, J. H., Fu, T.-M., Jacob, D. J.,
and Heald, C. L.: Global modeling of secondary organic aerosol formation from aromatic
hydrocarbons: high- vs. low-yield pathways, Atmos. Chem. Phys., 8, 2405–2420,
https://doi.org/10.5194/acp-8-2405-2008, 2008.
Hettiyadura, A. P. S., Xu, L., Jayarathne, T., Skog, K., Guo, H., Weber, R.
J., Nenes, A., Keutsch, F. N., Ng, N. L., and Stone, E. A.: Source
apportionment of organic carbon in Centreville, AL using organosulfates in
organic tracer-based positive matrix factorization, Atmos. Environ., 186,
74–88, https://doi.org/10.1016/j.atmosenv.2018.05.007, 2018.
Hopke, P. K.: Review of receptor modeling methods for source apportionment,
J. Air Waste Manage., 66, 237–259, https://doi.org/10.1080/10962247.2016.1140693,
2016.
Iinuma, Y., Böge, O., Gnauk, T., and Herrmann, H.: Aerosol-chamber study
of the α-pinene/O3 reaction: Influence of particle acidity on
aerosol yields and products, Atmos. Environ., 38, 761–773,
https://doi.org/10.1016/j.atmosenv.2003.10.015, 2004.
Jaeckels, J. M., Bae, M.-S., and Schauer, J. J.: Positive matrix
factorization (PMF) analysis of molecular marker measurements to quantify
the sources of organic aerosols, Environ. Sci. Technol., 41, 5763–5769,
https://doi.org/10.1021/es062536b, 2007.
Jayarathne, T., Rathnayake, C. M., and Stone, E. A.: Local source impacts on
primary and secondary aerosols in the Midwestern United States, Atmos.
Environ., 130, 74–83, https://doi.org/10.1016/j.atmosenv.2015.09.058, 2016.
Kaltsonoudis, C., Kostenidou, E., Louvaris, E., Psichoudaki, M., Tsiligiannis, E.,
Florou, K., Liangou, A., and Pandis, S. N.: Characterization of fresh and aged organic
aerosol emissions from meat charbroiling, Atmos. Chem. Phys., 17, 7143–7155,
https://doi.org/10.5194/acp-17-7143-2017, 2017.
Kaulfus, A. S., Nair, U., Jaffe, D., Christopher, S. A., and Goodrick, S.:
Biomass burning smoke climatology of the United States: implications for
particulate matter air quality, Environ. Sci. Technol., 51, 11731–11741,
https://doi.org/10.1021/acs.est.7b03292, 2017.
Kautzman, K. E., Surratt, J. D., Chan, M. N., Chan, A. W. H., Hersey, S. P.,
Chhabra, P. S., Dalleska, N. F., Wennberg, P. O., Flagan, R. C., and
Seinfeld, J. H.: Chemical composition of gas- and aerosol-phase products
from the photooxidation of naphthalene, J. Phys. Chem. A, 114, 913–934,
https://doi.org/10.1021/jp908530s, 2010.
Khalili, N. R., Scheff, P. A., and Holsen, T. M.: PAH source fingerprints
for coke ovens, diesel and, gasoline engines, highway tunnels, and wood
combustion emissions, Atmos. Environ., 29, 533–542,
https://doi.org/10.1016/1352-2310(94)00275-P, 1995.
Kleindienst, T. E., Conver, T. S., McIver, C. D., and Edney, E. O.:
Determination of secondary organic aerosol products from the photooxidation
of toluene and their implications in ambient PM2.5, J. Atmos. Chem.,
47, 79–100, 2004.
Kleindienst, T. E., Jaoui, M., Lewandowski, M., Offenberg, J. H., Lewis, C.
W., Bhave, P. V., and Edney, E. O.: Estimates of the contributions of
biogenic and anthropogenic hydrocarbons to secondary organic aerosol at a
southeastern US location, Atmos. Environ., 41, 8288–8300,
https://doi.org/10.1016/j.atmosenv.2007.06.045, 2007.
Kleindienst, T. E., Jaoui, M., Lewandowski, M., Offenberg, J. H., and Docherty, K. S.:
The formation of SOA and chemical tracer compounds from the photooxidation of
naphthalene and its methyl analogs in the presence and absence of nitrogen oxides,
Atmos. Chem. Phys., 12, 8711–8726, https://doi.org/10.5194/acp-12-8711-2012, 2012.
Kroll, J. H. and Seinfeld, J. H.: Chemistry of secondary organic aerosol:
Formation and evolution of low-volatility organics in the atmosphere, Atmos.
Environ., 42, 3593–3624, https://doi.org/10.1016/j.atmosenv.2008.01.003, 2008.
Kroll, J. H., Donahue, N. M., Jimenez, J. L., Kessler, S. H., Canagaratna,
M. R., Wilson, K. R., Altieri, K. E., Mazzoleni, L. R., Wozniak, A. S., and
Bluhm, H.: Carbon oxidation state as a metric for describing the chemistry
of atmospheric organic aerosol, Nat. Chem., 3, 133–139, https://doi.org/10.1038/nchem.948,
2011.
Lee, S., Baumann, K., Schauer, J. J., Sheesley, R. J., Naeher, L. P.,
Meinardi, S., Blake, D. R., Edgerton, E. S., Russell, A. G., and Clements,
M.: Gaseous and particulate emissions from prescribed burning in Georgia,
Environ. Sci. Technol., 39, 9049–9056, https://doi.org/10.1021/es051583l, 2005.
Levy, M. E., Zhang, R., Khalizov, A. F., Zheng, J., Collins, D. R., Glen, C.
R., Wang, Y., Yu, X.-Y., Luke, W., Jayne, J. T., and Olaguer, E.:
Measurements of submicron aerosols in Houston, Texas during the 2009 SHARP
field campaign, J. Geophys. Res., 118, 10518–10534, https://doi.org/10.1002/jgrd.50785,
2013.
Lewandowski, M., Jaoui, M., Offenberg, J. H., Kleindienst, T. E., Edney, E.
O., Sheesley, R. J., and Schauer, J. J.: Primary and secondary contributions
to ambient PM in the midwestern United States, Environ. Sci. Technol., 42,
3303–3309, 10.1021/es0720412, 2008.
Lin, P., Liu, J., Shilling, J. E., Kathmann, S. M., Laskin, J., and Laskin,
A.: Molecular characterization of brown carbon (BrC) chromophores in
secondary organic aerosol generated from photo-oxidation of toluene, PCCP,
17, 23312–23325, https://doi.org/10.1039/C5CP02563J, 2015.
Lin, Y.-H., Knipping, E. M., Edgerton, E. S., Shaw, S. L., and Surratt, J. D.:
Investigating the influences of SO2 and NH3 levels on isoprene-derived secondary organic aerosol
formation using conditional sampling approaches, Atmos. Chem. Phys., 13, 8457–8470,
https://doi.org/10.5194/acp-13-8457-2013, 2013.
Lough, G. C., Christensen, C. G., Schauer, J. J., Tortorelli, J., Mani, E.,
Lawson, D. R., Clark, N. N., and Gabele, P. A.: Development of molecular
marker source profiles for emissions from on-road gasoline and diesel vehicle
fleets, J. Air Waste Manage., 57, 1190–1199,
https://doi.org/10.3155/1047-3289.57.10.1190, 2007.
Mohr, C., Huffman, J. A., Cubison, M. J., Aiken, A. C., Docherty, K. S.,
Kimmel, J. R., Ulbrich, I. M., Hannigan, M., and Jimenez, J. L.:
Characterization of primary organic aerosol emissions from meat cooking,
trash burning, and motor vehicles with high-resolution aerosol mass
spectrometry and comparison with ambient and chamber observations, Environ.
Sci. Technol., 43, 2443–2449, https://doi.org/10.1021/es8011518, 2009.
Mohr, C., DeCarlo, P. F., Heringa, M. F., Chirico, R., Slowik, J. G., Richter, R.,
Reche, C., Alastuey, A., Querol, X., Seco, R., Pen̈uelas, J., Jiménez, J. L., Crippa,
M., Zimmermann, R., Baltensperger, U., and Prévôt, A. S. H.: Identification and
quantification of organic aerosol from cooking and other sources in Barcelona using
aerosol mass spectrometer data, Atmos. Chem. Phys., 12, 1649–1665,
https://doi.org/10.5194/acp-12-1649-2012, 2012.
Ng, N. L., Kroll, J. H., Chan, A. W. H., Chhabra, P. S., Flagan, R. C., and Seinfeld,
J. H.: Secondary organic aerosol formation from m-xylene, toluene, and benzene, Atmos.
Chem. Phys., 7, 3909–3922, https://doi.org/10.5194/acp-7-3909-2007, 2007.
Ng, N. L., Canagaratna, M. R., Jimenez, J. L., Chhabra, P. S., Seinfeld, J. H., and
Worsnop, D. R.: Changes in organic aerosol composition with aging inferred from aerosol
mass spectra, Atmos. Chem. Phys., 11, 6465–6474, https://doi.org/10.5194/acp-11-6465-2011, 2011.
Nguyen, T. B., Bates, K. H., Crounse, J. D., Schwantes, R. H., Zhang, X.,
Kjaergaard, H. G., Surratt, J. D., Lin, P., Laskin, A., and Seinfeld, J. H.:
Mechanism of the hydroxyl radical oxidation of methacryloyl peroxynitrate
(MPAN) and its pathway toward secondary organic aerosol formation in the
atmosphere, PCCP, 17, 17914–17926, 2015.
Norris, G., Duvall, R., Brown, S., and Bai, S.: EPA positive matrix
factorization (PMF) 5.0 fundamentals and user guide, U.S. Environmental
Protection Agency, Office of Research and Development, Washington, DC 20460
(136 pp., 7 MB, April 2014, 600-R-14-108), 2014.
Oros, D. R. and Simoneit, B. R. T.: Identification and emission rates of
molecular tracers in coal smoke particulate matter, Fuel, 79, 515–536,
https://doi.org/10.1016/S0016-2361(99)00153-2, 2000.
Paatero, P. and Tapper, U.: Positive matrix factorization: A non-negative
factor model with optimal utilization of error estimates of data values,
Environmetrics, 5, 111–126, https://doi.org/10.1002/env.3170050203, 1994.
Paatero, P. and Hopke, P. K.: Discarding or downweighting high-noise
variables in factor analytic models, Anal. Chim. Acta, 490, 277–289,
https://doi.org/10.1016/S0003-2670(02)01643-4, 2003.
Paatero, P.: User's guide for positive matrix factorization programs PMF2 and
PMF3, Part 1: Tutorial,” University of Helsinki, Finland, available at:
http://helsinki.fi/~paatero/PMF/pmf2.zip (last access:
10 October 2018), 2013.
Park, C., Schade, G. W., and Boedeker, I.: Characteristics of the flux of
isoprene and its oxidation products in an urban area, J. Geophys. Res., 116, D21303,
https://doi.org/10.1029/2011JD015856, 2011.
Pathak, R. K., Wu, W. S., and Wang, T.: Summertime PM2.5 ionic species in four major cities of China:
nitrate formation in an ammonia-deficient atmosphere, Atmos. Chem. Phys.,
9, 1711–1722, https://doi.org/10.5194/acp-9-1711-2009, 2009.
Peng, J., Hu, M., Gong, Z., Tian, X., Wang, M., Zheng, J., Guo, Q., Cao, W.,
Lv, W., and Hu, W.: Evolution of secondary inorganic and organic aerosols
during transport: A case study at a regional receptor site, Environ.
Pollut., 218, 794–803, https://doi.org/10.1016/j.envpol.2016.08.003, 2016.
Rattanavaraha, W., Chu, K., Budisulistiorini, S. H., Riva, M., Lin, Y.-H., Edgerton,
E. S., Baumann, K., Shaw, S. L., Guo, H., King, L., Weber, R. J., Neff, M. E., Stone,
E. A., Offenberg, J. H., Zhang, Z., Gold, A., and Surratt, J. D.: Assessing the impact
of anthropogenic pollution on isoprene-derived secondary organic aerosol formation in
PM2.5 collected from the Birmingham, Alabama, ground site during the 2013 Southern
Oxidant and Aerosol Study, Atmos. Chem. Phys., 16, 4897–4914, https://doi.org/10.5194/acp-16-4897-2016, 2016.
Reyes-Villegas, E., Bannan, T., Le Breton, M., Mehra, A., Priestley, M.,
Percival, C., Coe, H., and Allan, J. D.: Online chemical characterization of
food-cooking organic aerosols: Implications for source apportionment,
Environ. Sci. Technol., 52, 5308–5318, https://doi.org/10.1021/acs.est.7b06278, 2018.
Robinson, A. L., Donahue, N. M., Shrivastava, M. K., Weitkamp, E. A., Sage,
A. M., Grieshop, A. P., Lane, T. E., Pierce, J. R., and Pandis, S. N.:
Rethinking organic aerosols: Semivolatile emissions and photochemical aging,
Science, 315, 1259–1262, https://doi.org/10.1126/science.1133061, 2007.
Roe, S. M., Spivey, M. D., Lindquist, H. C. H., P., and Huntley, R.:
National emissions inventory for commercial cooking, 13th International
Emission Inventory Conference, Clearwater, Fl, 2004.
Rogers, C. M. and Bowman, K. P.: Transport of smoke from the Central
American fires of 1998, J. Geophys. Res., 106, 28357–28368,
https://doi.org/10.1029/2000JD000187, 2001.
Rogge, W. F., Hildemann, L. M., Mazurek, M. A., Cass, G. R., and Simoneit,
B. R.: Sources of fine organic aerosol. 1. Charbroilers and meat cooking
operations, Environ. Sci. Technol., 25, 1112–1125, 1991.
Rogge, W. F., Hildemann, L. M., Mazurek, M. A., Cass, G. R., and Simoneit,
B. R.: Sources of fine organic aerosol, 2. Noncatalyst and catalyst-equipped
automobiles and heavy-duty diesel trucks, Environ. Sci. Technol., 27,
636–651, 1993a.
Rogge, W. F., Hildemann, L. M., Mazurek, M. A., Cass, G. R., and Simoneit,
B. R.: Sources of fine organic aerosol, 3. Road dust, tire debris, and
organometallic brake lining dust: roads as sources and sinks, Environ. Sci.
Technol., 27, 1892–1904, 1993b.
Rogge, W. F., Hildemann, L. M., Mazurek, M. A., Cass, G. R., and Simoneit,
B. R.: Sources of fine organic aerosol, 9. Pine, oak, and synthetic log
combustion in residential fireplaces, Environ. Sci. Technol., 32, 13–22,
1998.
Schauer, J. J., Kleeman, M. J., Cass, G. R., and Simoneit, B. R.:
Measurement of emissions from air pollution sources, 5. C1-C32 organic
compounds from gasoline-powered motor vehicles, Environ. Sci. Technol., 36,
1169–1180, https://doi.org/10.1021/es0108077, 2002.
Schauer, J. J., Mader, B. T., Deminter, J. T., Heidemann, G., Bae, M. S.,
Seinfeld, J. H., Flagan, R. C., Cary, R. A., Smith, D., Huebert, B. J.,
Bertram, T., Howell, S., Kline, J. T., Quinn, P., Bates, T., Turpin, B.,
Lim, H. J., Yu, J. Z., Yang, H., and Keywood, M. D.: ACE-Asia
intercomparison of a thermal-optical method for the determination of
particle-phase organic and elemental carbon, Environ. Sci. Technol., 37,
993–1001, 2003.
Seinfeld, J. H. and Pankow, J. F.: Organic atmospheric particulate
material, Annu. Rev. Phys. Chem., 54, 121–140,
https://doi.org/10.1146/annurev.physchem.54.011002.103756, 2003.
Shakya, K. M. and Griffin, R. J.: Secondary organic aerosol from
photooxidation of polycyclic aromatic hydrocarbons, Environ. Sci. Technol.,
44, 8134–8139, https://doi.org/10.1021/es1019417, 2010.
Sharkey, T. D., Singsaas, E. L., Vanderveer, P. J., and Geron, C.: Field
measurements of isoprene emission from trees in response to temperature and
light, Tree Physiol., 16, 649–654, https://doi.org/10.1093/treephys/16.7.649, 1996.
Sheesley, R. J., Nallathamby, P. D., Surratt, J. D., Lee, A., Lewandowski,
M., Offenberg, J. H., Jaoui, M., and Kleindienst, T. E.: Constraints on
primary and secondary particulate carbon sources using chemical tracer and
14C methods during CalNex-Bakersfield, Atmos. Environ., 166, 204–214,
https://doi.org/10.1016/j.atmosenv.2017.07.025, 2017.
Shrivastava, M. K., Subramanian, R., Rogge, W. F., and Robinson, A. L.:
Sources of organic aerosol: Positive matrix factorization of molecular
marker data and comparison of results from different source apportionment
models, Atmos. Environ., 41, 9353–9369,
https://doi.org/10.1016/j.atmosenv.2007.09.016, 2007.
Simoneit, B. R. T., Schauer, J. J., Nolte, C. G., Oros, D. R., Elias, V. O.,
Fraser, M. P., Rogge, W. F., and Cass, G. R.: Levoglucosan, a tracer for
cellulose in biomass burning and atmospheric particles, Atmos. Environ., 33,
173–182, 1999.
Srivastava, D., Favez, O., Bonnaire, N., Lucarelli, F., Haeffelin, M.,
Perraudin, E., Gros, V., Villenave, E., and Albinet, A.: Speciation of
organic fractions does matter for aerosol source apportionment, Part 2:
Intensive short-term campaign in the Paris area (France), Sci. Total
Environ., 634, 267–278, https://doi.org/10.1016/j.scitotenv.2018.03.296, 2018a.
Srivastava, D., Tomaz, S., Favez, O., Lanzafame, G. M., Golly, B., Besombes,
J. L., Alleman, L. Y., Jaffrezo, J. L., Jacob, V., Perraudin, E., Villenave,
E., and Albinet, A.: Speciation of organic fraction does matter for source
apportionment. Part 1: A one-year campaign in Grenoble (France), Sci. Total
Environ., 624, 1598–1611, https://doi.org/10.1016/j.scitotenv.2017.12.135, 2018b.
Stone, E. A., Zhou, J. B., Snyder, D. C., Rutter, A. P., Mieritz, M., and
Schauer, J. J.: A Comparison of Summertime Secondary Organic Aerosol Source
Contributions at Contrasting Urban Locations, Environ. Sci. Technol., 43,
3448–3454, https://doi.org/10.1021/es8025209, 2009.
Sullivan, D. W., Price, J. H., Lambeth, B., Sheedy, K. A., Savanich, K., and
Tropp, R. J.: Field study and source attribution for PM2.5 and PM10
with resulting reduction in concentrations in the neighborhood north of the
Houston Ship Channel based on voluntary efforts, J. Air Waste Manage., 63,
1070–1082, https://doi.org/10.1080/10962247.2013.775972, 2013.
Sun, Y.-L., Zhang, Q., Schwab, J. J., Demerjian, K. L., Chen, W.-N., Bae,
M.-S., Hung, H.-M., Hogrefe, O., Frank, B., Rattigan, O. V., and Lin, Y.-C.:
Characterization of the sources and processes of organic and inorganic aerosols
in New York city with a high-resolution time-of-flight aerosol mass apectrometer,
Atmos. Chem. Phys., 11, 1581–1602, https://doi.org/10.5194/acp-11-1581-2011, 2011.
Sun, Y., Du, W., Fu, P., Wang, Q., Li, J., Ge, X., Zhang, Q., Zhu, C., Ren, L., Xu, W.,
Zhao, J., Han, T., Worsnop, D. R., and Wang, Z.: Primary and secondary aerosols in
Beijing in winter: sources, variations and processes, Atmos. Chem. Phys., 16,
8309–8329, https://doi.org/10.5194/acp-16-8309-2016, 2016.
Surratt, J. D., Lewandowski, M., Offenberg, J. H., Jaoui, M., Kleindienst,
T. E., Edney, E. O., and Seinfeld, J. H.: Effect of acidity on secondary
organic aerosol formation from isoprene, Environ. Sci. Technol., 41,
5363–5369, https://doi.org/10.1021/es0704176, 2007.
TCEQ: Texas Commission on Environmental Quality Air Monitoring Sites,
available at: https://www.tceq.texas.gov/airquality/monops/sites (last
access: 10 October 2018), 2017.
Ulbrich, I. M., Canagaratna, M. R., Zhang, Q., Worsnop, D. R., and Jimenez, J. L.:
Interpretation of organic components from Positive Matrix Factorization of aerosol
mass spectrometric data, Atmos. Chem. Phys., 9, 2891–2918, https://doi.org/10.5194/acp-9-2891-2009, 2009.
US-EPA: National Ambient Air Quality Standards, available at:
https://www.epa.gov/criteria-air-pollutants/naaqs-table, last access:
8 September 2017.
Volkamer, R., Jimenez, J. L., San Martini, F., Dzepina, K., Zhang, Q.,
Salcedo, D., Molina, L. T., Worsnop, D. R., and Molina, M. J.: Secondary
organic aerosol formation from anthropogenic air pollution: Rapid and higher
than expected, Geophys. Res. Lett., 33, L17811, https://doi.org/10.1029/2006GL026899,
2006.
Wallace, H. W., Sanchez, N. P., Flynn, J. H., Erickson, M. H., Lefer, B. L.,
and Griffin, R. J.: Source apportionment of particulate matter and trace
gases near a major refinery near the Houston Ship Channel, Atmos. Environ.,
173, 16–29, https://doi.org/10.1016/j.atmosenv.2017.10.049, 2018.
Wang, J., Christopher, S. A., Nair, U., Reid, J. S., Prins, E. M., Szykman,
J., and Hand, J. L.: Mesoscale modeling of Central American smoke transport
to the United States: 1. “Top-down” assessment of emission strength and
diurnal variation impacts, J. Geophys. Res., 111, D14S92,
https://doi.org/10.1029/2005JD006720, 2006.
Wang, Q. Q., He, X., Huang, X. H. H., Griffith, S. M., Feng, Y. M., Zhang,
T., Zhang, Q. Y., Wu, D., and Yu, J. Z.: Impact of secondary organic aerosol
tracers on tracer-based source apportionment of organic carbon and
PM2.5: A case study in the Pearl River Delta, China, ACS Earth Space
Chem., 1, 562–571, https://doi.org/10.1021/acsearthspacechem.7b00088, 2017.
Watson, J. G., Cooper, J. A., and Huntzicker, J. J.: The effective variance
weighting for least squares calculations applied to the mass balance
receptor model, Atmos. Environ., 18, 1347–1355,
https://doi.org/10.1016/0004-6981(84)90043-X, 1984.
Williams, E. J., Lerner, B. M., Murphy, P. C., Herndon, S. C., and Zahniser,
M. S.: Emissions of NOx, SO2, CO, and HCHO from commercial marine shipping
during Texas Air Quality Study (TexAQS) 2006, J. Geophys. Res., 114, D21306,
https://doi.org/10.1029/2009JD012094, 2009.
Xie, Y. and Berkowitz, C. M.: The use of positive matrix factorization with
conditional probability functions in air quality studies: an application to
hydrocarbon emissions in Houston, Texas, Atmos. Environ., 40, 3070–3091,
https://doi.org/10.1016/j.atmosenv.2005.12.065, 2006.
Xu, L., Guo, H. Y., Boyd, C. M., Klein, M., Bougiatioti, A., Cerully, K. M.,
Hite, J. R., Isaacman-VanWertz, G., Kreisberg, N. M., Knote, C., Olson, K.,
Koss, A., Goldstein, A. H., Hering, S. V., de Gouw, J., Baumann, K., Lee, S.
H., Nenes, A., Weber, R. J., and Ng, N. L.: Effects of anthropogenic
emissions on aerosol formation from isoprene and monoterpenes in the
southeastern United States, P. Natl. Acad. Sci. USA, 112, 37–42,
https://doi.org/10.1073/pnas.1417609112, 2015.
Yan, B., Zheng, M., Hu, Y. T., Lee, S., Kim, H. K., and Russell, A. G.: Organic
composition of carbonaceous aerosols in an aged prescribed fire plume, Atmos. Chem.
Phys., 8, 6381–6394, https://doi.org/10.5194/acp-8-6381-2008, 2008.
Yokelson, R. J., Crounse, J. D., DeCarlo, P. F., Karl, T., Urbanski, S., Atlas, E.,
Campos, T., Shinozuka, Y., Kapustin, V., Clarke, A. D., Weinheimer, A., Knapp, D. J.,
Montzka, D. D., Holloway, J., Weibring, P., Flocke, F., Zheng, W., Toohey, D., Wennberg,
P. O., Wiedinmyer, C., Mauldin, L., Fried, A., Richter, D., Walega, J., Jimenez, J. L.,
Adachi, K., Buseck, P. R., Hall, S. R., and Shetter, R.: Emissions from biomass burning
in the Yucatan, Atmos. Chem. Phys., 9, 5785–5812, https://doi.org/10.5194/acp-9-5785-2009, 2009.
Zhang, H. and Ying, Q.: Secondary organic aerosol from polycyclic aromatic
hydrocarbons in Southeast Texas, Atmos. Environ., 55, 279–287,
https://doi.org/10.1016/j.atmosenv.2012.03.043, 2012.
Zhang, J. K., Wang, L. L., Wang, Y. H., and Wang, Y. S.: Submicron
aerosols during the Beijing Asia–Pacific Economic Cooperation conference in
2014, Atmos. Environ., 124, 224–231, https://doi.org/10.1016/j.atmosenv.2015.06.049,
2016.
Zhang, Q., Jimenez, J. L., Canagaratna, M. R., Ulbrich, I. M., Ng, N. L.,
Worsnop, D. R., and Sun, Y.: Understanding atmospheric organic aerosols via
factor analysis of aerosol mass spectrometry: a review, Anal. Bioanal.
Chem., 401, 3045–3067, https://doi.org/10.1007/s00216-011-5355-y, 2011.
Zhang, X., Craft, E., and Zhang, K.: Characterizing spatial variability of
air pollution from vehicle traffic around the Houston Ship Channel area,
Atmos. Environ., 161, 167–175, https://doi.org/10.1016/j.atmosenv.2017.04.032, 2017.
Short summary
By integrating newly developed tracers for anthropogenic secondary organic aerosol in source apportionment for the first time, we estimate that this source contributes 28 % of fine particle organic carbon in the Houston Ship Channel. Our approach can be used to evaluate anthropogenic, biogenic, and biomass burning contributions to secondary organic aerosols elsewhere in the world. Because anthropogenic emissions are potentially controllable, they provide an opportunity to improve air quality.
By integrating newly developed tracers for anthropogenic secondary organic aerosol in source...
Altmetrics
Final-revised paper
Preprint