Articles | Volume 8, issue 9
https://doi.org/10.5194/amt-8-3729-2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
https://doi.org/10.5194/amt-8-3729-2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Research article
| 
16 Sep 2015
Research article |
| 16 Sep 2015
Accuracy and precision of 14C-based source apportionment of organic and elemental carbon in aerosols using the Swiss_4S protocol
G. O. Mouteva
CORRESPONDING AUTHOR
Earth System Science, University of California, Irvine, CA, USA
S. M. Fahrni
Earth System Science, University of California, Irvine, CA, USA
now at: Eidgenössische Technische Hochschule (ETH), Zürich, Switzerland
G. M. Santos
Earth System Science, University of California, Irvine, CA, USA
J. T. Randerson
Earth System Science, University of California, Irvine, CA, USA
Y.-L. Zhang
Department of Chemistry and Biochemistry & Oeschger Centre for Climate Change Research, University of Bern, Bern, Switzerland
S. Szidat
Department of Chemistry and Biochemistry & Oeschger Centre for Climate Change Research, University of Bern, Bern, Switzerland
C. I. Czimczik
Earth System Science, University of California, Irvine, CA, USA
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Fabian Rey, Erika Gobet, Christoph Schwörer, Albert Hafner, Sönke Szidat, and Willy Tinner
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Marcel Bliedtner, Hans von Suchodoletz, Imke Schäfer, Caroline Welte, Gary Salazar, Sönke Szidat, Mischa Haas, Nathalie Dubois, and Roland Zech
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Paul D. Zander, Sönke Szidat, Darrell S. Kaufman, Maurycy Żarczyński, Anna I. Poraj-Górska, Petra Boltshauser-Kaltenrieder, and Martin Grosjean
Geochronology, 2, 63–79, https://doi.org/10.5194/gchron-2-63-2020, https://doi.org/10.5194/gchron-2-63-2020, 2020
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Recent technological advances allow researchers to obtain radiocarbon ages from smaller samples than previously possible. We investigate the reliability and precision of radiocarbon ages obtained from miniature (11–150 μg C) samples of terrestrial plant fragments taken from sediment cores from Lake Żabińskie, Poland. We further investigate how sampling density (the number of ages per 1000 years) and sample mass (which is related to age precision) influence the performance of age–depth models.
Yu-Chi Lin, Yan-Lin Zhang, Mei-Yi Fan, and Mengying Bao
Atmos. Chem. Phys., 20, 3999–4011, https://doi.org/10.5194/acp-20-3999-2020, https://doi.org/10.5194/acp-20-3999-2020, 2020
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(1) Nitrate was a dominant contributing species in water-soluble inorganic ions during the high PM2.5 events in Nanjing.
(2) Nitrate aerosols in Nanjing during the PM2.5 events were mainly produced by hydrolysis of N2O5 in preexisting aerosols under ammonium-rich regimes.
(3) Control in NOx emissions would inhibit production of nitrate aerosols since NH4NO3 formation was HNO3 limited in Nanjing.
Jun Zhu, Xiangao Xia, Huizheng Che, Jun Wang, Zhiyuan Cong, Tianliang Zhao, Shichang Kang, Xuelei Zhang, Xingna Yu, and Yanlin Zhang
Atmos. Chem. Phys., 19, 14637–14656, https://doi.org/10.5194/acp-19-14637-2019, https://doi.org/10.5194/acp-19-14637-2019, 2019
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The long-term temporal–spatial variations of the aerosol optical properties over the Tibetan Plateau (TP) based on the multiple ground-based sun photometer sites and the MODIS product are presented. Besides, the aerosol pollution and aerosol transport processes over the TP are also analyzed by the observations and models. The results in this region could help reduce the assessment uncertainties of aerosol radiative forcing and provide more information on aerosol transportation.
Yunhua Chang, Yan-Lin Zhang, Jiarong Li, Chongguo Tian, Linlin Song, Xiaoyao Zhai, Wenqi Zhang, Tong Huang, Yu-Chi Lin, Chao Zhu, Yunting Fang, Moritz F. Lehmann, and Jianmin Chen
Atmos. Chem. Phys., 19, 12221–12234, https://doi.org/10.5194/acp-19-12221-2019, https://doi.org/10.5194/acp-19-12221-2019, 2019
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The present work underscores the value of cloud water dissolved inorganic nitrogen isotopes as carriers of quantitative information on regional NOx and NH3 emissions. It sheds light on the origin and production pathways of nitrogenous species in clouds and emphasizes the importance of biomass-burning-derived nitrogenous species as cloud condensation nuclei in China’s troposphere. Moreover, it highlights the rapid evolution of NOx emissions in China.
Xiaoyan Liu, Yan-Lin Zhang, Yiran Peng, Lulu Xu, Chunmao Zhu, Fang Cao, Xiaoyao Zhai, M. Mozammel Haque, Chi Yang, Yunhua Chang, Tong Huang, Zufei Xu, Mengying Bao, Wenqi Zhang, Meiyi Fan, and Xuhui Lee
Atmos. Chem. Phys., 19, 11213–11233, https://doi.org/10.5194/acp-19-11213-2019, https://doi.org/10.5194/acp-19-11213-2019, 2019
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Although a total ban on straw burning has been enforced in eastern China, the regionally transported biomass burning emissions remarkably impacted the chemical and optical properties of carbonaceous aerosols in Nanjing, which were quantified by a calculation based on measured data and a simulation based on a model. Results showed that regionally transported biomass burning emissions significantly contributed to the carbonaceous aerosols and impacted the solar radiation balance of the atmosphere.
Wenqi Zhang, Yan-Lin Zhang, Fang Cao, Yankun Xiang, Yuanyuan Zhang, Mengying Bao, Xiaoyan Liu, and Yu-Chi Lin
Atmos. Chem. Phys., 19, 11071–11087, https://doi.org/10.5194/acp-19-11071-2019, https://doi.org/10.5194/acp-19-11071-2019, 2019
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A novel method to determine the concentration and the isotopes of WSOC in aerosols is established and applied in the analysis of a severe haze in eastern China. The results show that the studied site is affected by the photochemical aging, biomass burning and dust aerosols in different episodes during the sampling period. The analysis of WSOC and its isotopes offers a great potential to better understand the source emission, the atmospheric aging and the secondary production of WSOC.
Tak W. Chan, Lin Huang, Kulbir Banwait, Wendy Zhang, Darrell Ernst, Xiaoliang Wang, John G. Watson, Judith C. Chow, Mark Green, Claudia I. Czimczik, Guaciara M. Santos, Sangeeta Sharma, and Keith Jones
Atmos. Meas. Tech., 12, 4543–4560, https://doi.org/10.5194/amt-12-4543-2019, https://doi.org/10.5194/amt-12-4543-2019, 2019
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This study compared 10 years of carbonaceous aerosol measurements collected at Egbert by three North American long-term monitoring networks. The study evaluated how differences in sample collection and analysis affected the concentrations of total carbon (TC), organic carbon (OC), and elemental carbon (EC). Various carbonaceous fractions measured by the three networks were consistent and comparable over the period. Elevated OC and EC were observed when ambient temperature exceeded 10 °C.
Md. Mozammel Haque, Kimitaka Kawamura, Dhananjay K. Deshmukh, Cao Fang, Wenhuai Song, Bao Mengying, and Yan-Lin Zhang
Atmos. Chem. Phys., 19, 5147–5164, https://doi.org/10.5194/acp-19-5147-2019, https://doi.org/10.5194/acp-19-5147-2019, 2019
Karl Espen Yttri, David Simpson, Robert Bergström, Gyula Kiss, Sönke Szidat, Darius Ceburnis, Sabine Eckhardt, Christoph Hueglin, Jacob Klenø Nøjgaard, Cinzia Perrino, Ignazio Pisso, Andre Stephan Henry Prevot, Jean-Philippe Putaud, Gerald Spindler, Milan Vana, Yan-Lin Zhang, and Wenche Aas
Atmos. Chem. Phys., 19, 4211–4233, https://doi.org/10.5194/acp-19-4211-2019, https://doi.org/10.5194/acp-19-4211-2019, 2019
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Carbonaceous aerosols from natural sources were abundant regardless of season. Residential wood burning (RWB) emissions were occasionally equally as large as or larger than of fossil-fuel sources, depending on season and region. RWB emissions are poorly constrained; thus emissions inventories need improvement. Harmonizing emission factors between countries is likely the most important step to improve model calculations for biomass burning emissions and European PM2.5 concentrations in general.
Yu-Chi Lin, Shih-Chieh Hsu, Chuan-Yao Lin, Shuen-Hsin Lin, Yi-Tang Huang, Yunhua Chang, and Yan-Lin Zhang
Atmos. Chem. Phys., 18, 13865–13879, https://doi.org/10.5194/acp-18-13865-2018, https://doi.org/10.5194/acp-18-13865-2018, 2018
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The Asian continent is a well-known big source of airborne As in the North Pacific region. Previously, high As concentrations over the free troposphere in the region have been observed and considered contributions of industrial emissions, especially of coal-combustion. In our study, we proposed a new concept for a potential source of high As over the subtropical free troposphere, that is, BB activities over southern Asia might be an important source of airborne arsenic in the springtime.
Yunhua Chang, Kan Huang, Mingjie Xie, Congrui Deng, Zhong Zou, Shoudong Liu, and Yanlin Zhang
Atmos. Chem. Phys., 18, 11793–11812, https://doi.org/10.5194/acp-18-11793-2018, https://doi.org/10.5194/acp-18-11793-2018, 2018
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We continuously performed a one-year and hourly-resolved measurement of 18 atmospheric elements in PM2.5 in Shanghai megacity. Here our high time-resolution observations over a long-term period provide baseline data with high detail, which are of great use for examining acute exposure of morbidity and mortality risk in association with PM2.5 metal species in China's megacities.
Yunhua Chang, Yanlin Zhang, Chongguo Tian, Shichun Zhang, Xiaoyan Ma, Fang Cao, Xiaoyan Liu, Wenqi Zhang, Thomas Kuhn, and Moritz F. Lehmann
Atmos. Chem. Phys., 18, 11647–11661, https://doi.org/10.5194/acp-18-11647-2018, https://doi.org/10.5194/acp-18-11647-2018, 2018
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We demonstrate that it is imperative that future studies, making use of isotope mixing models to gain conclusive constraints on the source partitioning of atmospheric NOx, consider this N isotope fractionation. Future assessments of NOx emissions in China (and elsewhere) should involve simultaneous δ15N and δ18O measurements of atmospheric nitrate and NOx at high spatiotemporal resolution, allowing former N-isotope-based NOx source partitioning estimates to be reevaluated more quantitatively.
Arineh Cholakian, Matthias Beekmann, Augustin Colette, Isabelle Coll, Guillaume Siour, Jean Sciare, Nicolas Marchand, Florian Couvidat, Jorge Pey, Valerie Gros, Stéphane Sauvage, Vincent Michoud, Karine Sellegri, Aurélie Colomb, Karine Sartelet, Helen Langley DeWitt, Miriam Elser, André S. H. Prévot, Sonke Szidat, and François Dulac
Atmos. Chem. Phys., 18, 7287–7312, https://doi.org/10.5194/acp-18-7287-2018, https://doi.org/10.5194/acp-18-7287-2018, 2018
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In this work, four schemes for the simulation of organic aerosols in the western Mediterranean basin are added to the CHIMERE chemistry–transport model; the resulting simulations are then compared to measurements obtained from ChArMEx. It is concluded that the scheme taking into account the fragmentation and the formation of nonvolatile organic aerosols corresponds better to measurements; the major source of this aerosol in the western Mediterranean is found to be of biogenic origin.
Athanasia Vlachou, Kaspar R. Daellenbach, Carlo Bozzetti, Benjamin Chazeau, Gary A. Salazar, Soenke Szidat, Jean-Luc Jaffrezo, Christoph Hueglin, Urs Baltensperger, Imad El Haddad, and André S. H. Prévôt
Atmos. Chem. Phys., 18, 6187–6206, https://doi.org/10.5194/acp-18-6187-2018, https://doi.org/10.5194/acp-18-6187-2018, 2018
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Carbonaceous aerosols are related to adverse human health effects, which depend on the aerosol chemical composition and size. Here, we combine aerosol mass spectrometry and radiocarbon measurements of size-resolved samples collected over a long term to identify the origins of primary and secondary carbonaceous aerosols in the fine and coarse modes.
Di Liu, Matthias Vonwiller, Jun Li, Junwen Liu, Sönke Szidat, Yanlin Zhang, Chongguo Tian, Yinjun Chen, Zhineng Cheng, Guangcai Zhong, Pingqing Fu, and Gan Zhang
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2018-295, https://doi.org/10.5194/acp-2018-295, 2018
Revised manuscript not accepted
Yan-Lin Zhang, Imad El-Haddad, Ru-Jin Huang, Kin-Fai Ho, Jun-Ji Cao, Yongming Han, Peter Zotter, Carlo Bozzetti, Kaspar R. Daellenbach, Jay G. Slowik, Gary Salazar, André S. H. Prévôt, and Sönke Szidat
Atmos. Chem. Phys., 18, 4005–4017, https://doi.org/10.5194/acp-18-4005-2018, https://doi.org/10.5194/acp-18-4005-2018, 2018
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Here we present a quantitative source apportionment of WSOC, isolated from aerosols in China using radiocarbon (14C) and offline high-resolution time of flight aerosol mass spectrometer measurements. We demonstrate a dominant contribution of non-fossil emissions to WSOC aerosols in the Northern Hemisphere. However, the fossil fraction is substantially larger in aerosols from East Asia and the east Asian pollution outflow, especially during winter, due to increasing coal combustion.
Kaspar R. Daellenbach, Imad El-Haddad, Lassi Karvonen, Athanasia Vlachou, Joel C. Corbin, Jay G. Slowik, Maarten F. Heringa, Emily A. Bruns, Samuel M. Luedin, Jean-Luc Jaffrezo, Sönke Szidat, Andrea Piazzalunga, Raquel Gonzalez, Paola Fermo, Valentin Pflueger, Guido Vogel, Urs Baltensperger, and André S. H. Prévôt
Atmos. Chem. Phys., 18, 2155–2174, https://doi.org/10.5194/acp-18-2155-2018, https://doi.org/10.5194/acp-18-2155-2018, 2018
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A novel offline LDI-MS method was developed to analyse particulate matter (PM) collected at multiple sites in central Europe during the entire year of 2013. PM sources were identified by positive matrix factorization. Wood burning emissions were separated according to the burning conditions; inefficient burns had a larger impact on air quality in southern Alpine valleys than in northern Switzerland. Moreover, primary tailpipe exhaust was distinguished from aged/secondary traffic emissions.
Marcel Lerch, Marcel Bliedtner, Christopher-Bastian Roettig, Jan-Uwe Schmidt, Sönke Szidat, Gary Salazar, Roland Zech, Bruno Glaser, Arno Kleber, and Michael Zech
E&G Quaternary Sci. J., 66, 103–108, https://doi.org/10.5194/egqsj-66-103-2018, https://doi.org/10.5194/egqsj-66-103-2018, 2018
Lorenz Wüthrich, Marcel Bliedtner, Imke Kathrin Schäfer, Jana Zech, Fatemeh Shajari, Dorian Gaar, Frank Preusser, Gary Salazar, Sönke Szidat, and Roland Zech
E&G Quaternary Sci. J., 66, 91–100, https://doi.org/10.5194/egqsj-66-91-2017, https://doi.org/10.5194/egqsj-66-91-2017, 2017
Tesfaye A. Berhanu, Sönke Szidat, Dominik Brunner, Ece Satar, Rüdiger Schanda, Peter Nyfeler, Michael Battaglia, Martin Steinbacher, Samuel Hammer, and Markus Leuenberger
Atmos. Chem. Phys., 17, 10753–10766, https://doi.org/10.5194/acp-17-10753-2017, https://doi.org/10.5194/acp-17-10753-2017, 2017
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Fossil fuel CO2 is the major contributor of anthropogenic CO2 in the atmosphere, and accurate quantification is essential to better understand the carbon cycle. Such accurate quantification can be conducted based on radiocarbon measurements. In this study, we present radiocarbon measurements from a tall tower site in Switzerland. From these measurements, we have observed seasonally varying fossil fuel CO2 contributions and a biospheric CO2 component that varies diurnally and seasonally.
Yunhua Chang, Congrui Deng, Fang Cao, Chang Cao, Zhong Zou, Shoudong Liu, Xuhui Lee, Jun Li, Gan Zhang, and Yanlin Zhang
Atmos. Chem. Phys., 17, 9945–9964, https://doi.org/10.5194/acp-17-9945-2017, https://doi.org/10.5194/acp-17-9945-2017, 2017
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This paper presents the results from a 5-year and near-real-time measurement study of carbonaceous aerosols in PM2.5 conducted at an urban site in Shanghai. Moreover, we integrated the results from historical field measurements and satellite observations, concluding that carbonaceous aerosol pollution in Shanghai has gradually reduced since 2006. This can be largely explained by the introduction of air-cleaning measures such as controlling vehicular emissions.
Prettiny K. Ma, Yunliang Zhao, Allen L. Robinson, David R. Worton, Allen H. Goldstein, Amber M. Ortega, Jose L. Jimenez, Peter Zotter, André S. H. Prévôt, Sönke Szidat, and Patrick L. Hayes
Atmos. Chem. Phys., 17, 9237–9259, https://doi.org/10.5194/acp-17-9237-2017, https://doi.org/10.5194/acp-17-9237-2017, 2017
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Airborne particulate matter (PM) negatively impacts air quality in cities throughout the world. An important fraction of PM is organic aerosol. We have evaluated and developed several new models for secondary organic aerosol (SOA), which is formed from the chemical processing of gaseous precursors. Using our model results, we have quantified important SOA sources and precursors and also identified possible model parameterizations that could be used for air quality predictions.
Vincent Michoud, Jean Sciare, Stéphane Sauvage, Sébastien Dusanter, Thierry Léonardis, Valérie Gros, Cerise Kalogridis, Nora Zannoni, Anaïs Féron, Jean-Eudes Petit, Vincent Crenn, Dominique Baisnée, Roland Sarda-Estève, Nicolas Bonnaire, Nicolas Marchand, H. Langley DeWitt, Jorge Pey, Aurélie Colomb, François Gheusi, Sonke Szidat, Iasonas Stavroulas, Agnès Borbon, and Nadine Locoge
Atmos. Chem. Phys., 17, 8837–8865, https://doi.org/10.5194/acp-17-8837-2017, https://doi.org/10.5194/acp-17-8837-2017, 2017
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The ChArMEx SOP2 field campaign took place from 15 July to 5 August 2013 in the western Mediterranean Basin at Ersa, a remote site in Cape Corse. Exhaustive descriptions of the chemical composition of air masses in gas and aerosol phase were performed. An analysis of these measurements was performed using various source-receptor approaches. This led to the identification of several factors linked to primary sources but also to secondary processes of both biogenic and anthropogenic origin.
Célia J. Sapart, Natalia Shakhova, Igor Semiletov, Joachim Jansen, Sönke Szidat, Denis Kosmach, Oleg Dudarev, Carina van der Veen, Matthias Egger, Valentine Sergienko, Anatoly Salyuk, Vladimir Tumskoy, Jean-Louis Tison, and Thomas Röckmann
Biogeosciences, 14, 2283–2292, https://doi.org/10.5194/bg-14-2283-2017, https://doi.org/10.5194/bg-14-2283-2017, 2017
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The Arctic Ocean, especially the Siberian shelves, overlays large areas of subsea permafrost that is degrading. We show that methane with a biogenic origin is emitted from this permafrost. At locations where bubble plumes have been observed, methane can escape oxidation in the surface sediment and rapidly migrate through the very shallow water column of this region to escape to the atmosphere, generating a positive radiative feedback.
Peter Zotter, Hanna Herich, Martin Gysel, Imad El-Haddad, Yanlin Zhang, Griša Močnik, Christoph Hüglin, Urs Baltensperger, Sönke Szidat, and André S. H. Prévôt
Atmos. Chem. Phys., 17, 4229–4249, https://doi.org/10.5194/acp-17-4229-2017, https://doi.org/10.5194/acp-17-4229-2017, 2017
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Most studies use a single Ångström exponent for wood burning (αWB) and traffic (αTR) emissions in the Aethalometer model, used for source apportionment of black carbon, derived from previous work. However, accurate determination of the α values is currently lacking. Comparing radiocarbon measurements (14C) with the Aehtalometer model, good agreement was found, indicating that the Aethalometer model reproduces reasonably well the 14C results using our best estimate of a single αWB and αTR.
Ulrike Dusek, Regina Hitzenberger, Anne Kasper-Giebl, Magdalena Kistler, Harro A. J. Meijer, Sönke Szidat, Lukas Wacker, Rupert Holzinger, and Thomas Röckmann
Atmos. Chem. Phys., 17, 3233–3251, https://doi.org/10.5194/acp-17-3233-2017, https://doi.org/10.5194/acp-17-3233-2017, 2017
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Measurements of the radioactive carbon isotope 14C allow to identify the sources of aerosol carbon. We report an extensive 14C source apportionment record in the Netherlands with samples covering a whole year. We discovered that long-range transport has a large influence on aerosol carbon levels. Fossil fuel carbon is least influenced by long-range transport and more regional in origin. Biomass burning seems to be a minor source of aerosol carbon in the Netherlands.
Chiara Uglietti, Alexander Zapf, Theo Manuel Jenk, Michael Sigl, Sönke Szidat, Gary Salazar, and Margit Schwikowski
The Cryosphere, 10, 3091–3105, https://doi.org/10.5194/tc-10-3091-2016, https://doi.org/10.5194/tc-10-3091-2016, 2016
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A meaningful interpretation of the climatic history contained in ice cores requires a precise chronology. For dating the older and deeper part of the glaciers, radiocarbon analysis can be used when organic matter such as plant or insect fragments are found in the ice. Since this happens rarely, a complementary dating tool, based on radiocarbon dating of the insoluble fraction of carbonaceous aerosols entrapped in the ice, allows for ice dating between 200 and more than 10 000 years.
Jianzhong Xu, Jinsen Shi, Qi Zhang, Xinlei Ge, Francesco Canonaco, André S. H. Prévôt, Matthias Vonwiller, Sönke Szidat, Jinming Ge, Jianmin Ma, Yanqing An, Shichang Kang, and Dahe Qin
Atmos. Chem. Phys., 16, 14937–14957, https://doi.org/10.5194/acp-16-14937-2016, https://doi.org/10.5194/acp-16-14937-2016, 2016
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This study deployed an AMS field study in Lanzhou, a city in northwestern China, evaluating the chemical composition, sources, and processes of urban aerosols during wintertime. In comparison with the results during summer in Lanzhou, the air pollution during winter was more severe and the sources were more complex. In addition, this paper estimates the contributions of fossil and non-fossil sources of organic carbon to primary and secondary organic carbon using the carbon isotopic method.
Weiwei Fu, James T. Randerson, and J. Keith Moore
Biogeosciences, 13, 5151–5170, https://doi.org/10.5194/bg-13-5151-2016, https://doi.org/10.5194/bg-13-5151-2016, 2016
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Global NPP and EP are reduced considerably for RCP8.5. Negative response of NPP and EP to stratification increases reflects a bottom-up control. Models with dynamic phytoplankton community structure show larger declines in EP than in NPP driven by phytoplankton community composition shifts. Projections of the NPP response to climate change depend on the phytoplankton community structure, the efficiency of the biological pump and the levels of regenerated production.
Chris D. Jones, Vivek Arora, Pierre Friedlingstein, Laurent Bopp, Victor Brovkin, John Dunne, Heather Graven, Forrest Hoffman, Tatiana Ilyina, Jasmin G. John, Martin Jung, Michio Kawamiya, Charlie Koven, Julia Pongratz, Thomas Raddatz, James T. Randerson, and Sönke Zaehle
Geosci. Model Dev., 9, 2853–2880, https://doi.org/10.5194/gmd-9-2853-2016, https://doi.org/10.5194/gmd-9-2853-2016, 2016
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How the carbon cycle interacts with climate will affect future climate change and how society plans emissions reductions to achieve climate targets. The Coupled Climate Carbon Cycle Model Intercomparison Project (C4MIP) is an endorsed activity of CMIP6 and aims to quantify these interactions and feedbacks in state-of-the-art climate models. This paper lays out the experimental protocol for modelling groups to follow to contribute to C4MIP. It is a contribution to the CMIP6 GMD Special Issue.
Yan-Lin Zhang, Kimitaka Kawamura, Ping Qing Fu, Suresh K. R. Boreddy, Tomomi Watanabe, Shiro Hatakeyama, Akinori Takami, and Wei Wang
Atmos. Chem. Phys., 16, 6407–6419, https://doi.org/10.5194/acp-16-6407-2016, https://doi.org/10.5194/acp-16-6407-2016, 2016
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Here, based on three aircraft measurements over East Asia, we demonstrate an aqueous-phase mechanism for enhanced SOA production in the troposphere following correlation analysis of oxalic acid in tropospheric aerosols with other measured chemical variables including its precursors and its intermediate as well as biogenic-derived SOA from isoprene, monoterpenes and β-caryophyllene.
Vidmantas Ulevicius, Steigvilė Byčenkienė, Carlo Bozzetti, Athanasia Vlachou, Kristina Plauškaitė, Genrik Mordas, Vadimas Dudoitis, Gülcin Abbaszade, Vidmantas Remeikis, Andrius Garbaras, Agne Masalaite, Jan Blees, Roman Fröhlich, Kaspar R. Dällenbach, Francesco Canonaco, Jay G. Slowik, Josef Dommen, Ralf Zimmermann, Jürgen Schnelle-Kreis, Gary A. Salazar, Konstantinos Agrios, Sönke Szidat, Imad El Haddad, and André S. H. Prévôt
Atmos. Chem. Phys., 16, 5513–5529, https://doi.org/10.5194/acp-16-5513-2016, https://doi.org/10.5194/acp-16-5513-2016, 2016
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In early spring the Baltic region is frequently affected by high pollution events due to biomass burning in that area. Here we present a comprehensive study to investigate the impact of biomass/grass burning (BB) on the evolution and composition of aerosol in Preila, Lithuania, during springtime open fires.
Anne Alexandre, Jérôme Balesdent, Patrick Cazevieille, Claire Chevassus-Rosset, Patrick Signoret, Jean-Charles Mazur, Araks Harutyunyan, Emmanuel Doelsch, Isabelle Basile-Doelsch, Hélène Miche, and Guaciara M. Santos
Biogeosciences, 13, 1693–1703, https://doi.org/10.5194/bg-13-1693-2016, https://doi.org/10.5194/bg-13-1693-2016, 2016
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This 13C labeling experiment demonstrates that carbon can be absorbed by the roots, translocated in the plant, and ultimately fixed in organic compounds subject to occlusion in silica particles that form inside plant cells (phytoliths). Plausible forms of carbon absorbed, translocated, and fixed in phytoliths are assessed. Implications for our understanding of the C cycle at the plant-soil-atmosphere interface are discussed.
Junwen Liu, Jun Li, Di Liu, Ping Ding, Chengde Shen, Yangzhi Mo, Xinming Wang, Chunling Luo, Zhineng Cheng, Sönke Szidat, Yanlin Zhang, Yingjun Chen, and Gan Zhang
Atmos. Chem. Phys., 16, 2985–2996, https://doi.org/10.5194/acp-16-2985-2016, https://doi.org/10.5194/acp-16-2985-2016, 2016
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Many Chinese cities now are suffering the high loadings of fine particular matters, which can bring a lot of negative impacts on air quality, human health, and the climate system. The Chinese government generally focuses on the control of the emissions from vehicles and industry. Our results evidently show that the burning of biomass materials such as wood and agricultural residues can lead to the urban air pollution in China. The characteristic of haze covering China is distinct from regions.
Paul E. Reyerson, Anne Alexandre, Araks Harutyunyan, Remi Corbineau, Hector A. Martinez De La Torre, Franz Badeck, Luigi Cattivelli, and Guaciara M. Santos
Biogeosciences, 13, 1269–1286, https://doi.org/10.5194/bg-13-1269-2016, https://doi.org/10.5194/bg-13-1269-2016, 2016
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We characterize the origin of carbon (C) in phytoliths (biosilica of higher plants) by a multi-isotope approach. We show that phytoliths occlude soil organic C adsorbed through the roots, making them unsuitable for paleo-proxy studies, 14C dating or atmospheric CO2 sequestration. Our findings are in parallel with recent soil paradigm shifts showing that soil microbes access old C and therefore call for further investigations on the role of old C in root–plant interactions and biomineralization.
K. R. Daellenbach, C. Bozzetti, A. Křepelová, F. Canonaco, R. Wolf, P. Zotter, P. Fermo, M. Crippa, J. G. Slowik, Y. Sosedova, Y. Zhang, R.-J. Huang, L. Poulain, S. Szidat, U. Baltensperger, I. El Haddad, and A. S. H. Prévôt
Atmos. Meas. Tech., 9, 23–39, https://doi.org/10.5194/amt-9-23-2016, https://doi.org/10.5194/amt-9-23-2016, 2016
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In this study, we developed an offline technique using the AMS for the characterization of the chemical fingerprints of aerosols collected on quartz filters, and evaluated the suitability of the organic mass spectral data for source apportionment. This technique may be used to enhance the AMS capabilities in measuring size-fractionated, spatially resolved long-term data sets.
S. E. Bush, F. M. Hopkins, J. T. Randerson, C.-T. Lai, and J. R. Ehleringer
Atmos. Meas. Tech., 8, 3481–3492, https://doi.org/10.5194/amt-8-3481-2015, https://doi.org/10.5194/amt-8-3481-2015, 2015
S. Veraverbeke, B. M. Rogers, and J. T. Randerson
Biogeosciences, 12, 3579–3601, https://doi.org/10.5194/bg-12-3579-2015, https://doi.org/10.5194/bg-12-3579-2015, 2015
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We developed a statistical model of daily carbon consumption by fire for Alaska at 450m resolution between 2001 and 2012. We used field measurements from black spruce forests in Alaska to build nonlinear multiplicative models predicting carbon consumption by fire in response to environmental variables. Our analysis highlights the importance of accounting for the spatial heterogeneity within fuels and consumption when extrapolating emissions in space and time.
P. L. Hayes, A. G. Carlton, K. R. Baker, R. Ahmadov, R. A. Washenfelder, S. Alvarez, B. Rappenglück, J. B. Gilman, W. C. Kuster, J. A. de Gouw, P. Zotter, A. S. H. Prévôt, S. Szidat, T. E. Kleindienst, J. H. Offenberg, P. K. Ma, and J. L. Jimenez
Atmos. Chem. Phys., 15, 5773–5801, https://doi.org/10.5194/acp-15-5773-2015, https://doi.org/10.5194/acp-15-5773-2015, 2015
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(1) Four different parameterizations for the formation and chemical evolution of secondary organic aerosol (SOA) are evaluated using a box model representing the Los Angeles region during the CalNex campaign.
(2) The SOA formed only from the oxidation of VOCs is insufficient to explain the observed SOA concentrations.
(3) The amount of SOA mass formed from diesel vehicle emissions is estimated to be 16-27%.
(4) Modeled SOA depends strongly on the P-S/IVOC volatility distribution.
J. P. Krüger, J. Leifeld, S. Glatzel, S. Szidat, and C. Alewell
Biogeosciences, 12, 2861–2871, https://doi.org/10.5194/bg-12-2861-2015, https://doi.org/10.5194/bg-12-2861-2015, 2015
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Biogeochemical soil parameters are studied to detect peatland degradation along a land use gradient (intensive, extensive, near-natural). Stable carbon isotopes, radiocarbon ages and ash content confirm peat growth in the near-natural bog but also indicate previous degradation. When the bog is managed extensively or intensively as grassland, all parameters indicate degradation and substantial C loss of the order of 18.8 to 42.9 kg C m-2.
L. R. Crilley, W. J. Bloss, J. Yin, D. C. S. Beddows, R. M. Harrison, J. D. Allan, D. E. Young, M. Flynn, P. Williams, P. Zotter, A. S. H. Prevot, M. R. Heal, J. F. Barlow, C. H. Halios, J. D. Lee, S. Szidat, and C. Mohr
Atmos. Chem. Phys., 15, 3149–3171, https://doi.org/10.5194/acp-15-3149-2015, https://doi.org/10.5194/acp-15-3149-2015, 2015
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Wood is a renewable fuel but its combustion for residential heating releases a number of locally acting air pollutants, most notably particulate matter known to have adverse effects on human health. This paper used chemical tracers for wood smoke to estimate the contribution that burning wood makes to concentrations of airborne particles in the atmosphere of southern England and most particularly in London.
A. Alexandre, I. Basile-Doelsch, T. Delhaye, D. Borshneck, J. C. Mazur, P. Reyerson, and G. M. Santos
Biogeosciences, 12, 863–873, https://doi.org/10.5194/bg-12-863-2015, https://doi.org/10.5194/bg-12-863-2015, 2015
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Phytoliths contain occluded organic compounds called phytC. The nature and location of phytC in biogenic silica structures is poorly understood. Here, we reconstructed the 3-D structure of phytoliths using 3-D Xray microscopy. We further evidenced a pool of phytC, continuously distributed in the silica structure, using nanoscale secondary ion mass spectrometry (NanoSIMS). Our findings allowed the re-evaluation of previous suggestions regarding phytC quantification and environmental meaning.
Y.-L. Zhang, R.-J. Huang, I. El Haddad, K.-F. Ho, J.-J. Cao, Y. Han, P. Zotter, C. Bozzetti, K. R. Daellenbach, F. Canonaco, J. G. Slowik, G. Salazar, M. Schwikowski, J. Schnelle-Kreis, G. Abbaszade, R. Zimmermann, U. Baltensperger, A. S. H. Prévôt, and S. Szidat
Atmos. Chem. Phys., 15, 1299–1312, https://doi.org/10.5194/acp-15-1299-2015, https://doi.org/10.5194/acp-15-1299-2015, 2015
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Source apportionment of fine carbonaceous aerosols using radiocarbon and other organic markers measurements during 2013 winter haze episodes was conducted at four megacities in China. Our results demonstrate that fossil emissions predominate EC with a mean contribution of 75±8%, whereas non-fossil sources account for 55±10% of OC; and the increment of TC on heavily polluted days was mainly driven by the increase of secondary OC from both fossil-fuel and non-fossil emissions.
P. Zotter, V. G. Ciobanu, Y. L. Zhang, I. El-Haddad, M. Macchia, K. R. Daellenbach, G. A. Salazar, R.-J. Huang, L. Wacker, C. Hueglin, A. Piazzalunga, P. Fermo, M. Schwikowski, U. Baltensperger, S. Szidat, and A. S. H. Prévôt
Atmos. Chem. Phys., 14, 13551–13570, https://doi.org/10.5194/acp-14-13551-2014, https://doi.org/10.5194/acp-14-13551-2014, 2014
M. Lupascu, J. M. Welker, U. Seibt, X. Xu, I. Velicogna, D. S. Lindsey, and C. I. Czimczik
Biogeosciences, 11, 4289–4304, https://doi.org/10.5194/bg-11-4289-2014, https://doi.org/10.5194/bg-11-4289-2014, 2014
F. Sedano and J. T. Randerson
Biogeosciences, 11, 3739–3755, https://doi.org/10.5194/bg-11-3739-2014, https://doi.org/10.5194/bg-11-3739-2014, 2014
C. de Linage, J. S. Famiglietti, and J. T. Randerson
Hydrol. Earth Syst. Sci., 18, 2089–2102, https://doi.org/10.5194/hess-18-2089-2014, https://doi.org/10.5194/hess-18-2089-2014, 2014
K. E. O. Todd-Brown, J. T. Randerson, F. Hopkins, V. Arora, T. Hajima, C. Jones, E. Shevliakova, J. Tjiputra, E. Volodin, T. Wu, Q. Zhang, and S. D. Allison
Biogeosciences, 11, 2341–2356, https://doi.org/10.5194/bg-11-2341-2014, https://doi.org/10.5194/bg-11-2341-2014, 2014
Related subject area
Subject: Aerosols | Technique: Laboratory Measurement | Topic: Validation and Intercomparisons
Pressure-dependent performance of two CEN-specified condensation particle counters
Characterisation of a self-sustained, water-based condensation particle counter for aircraft cruising pressure level operation
Importance of size representation and morphology in modelling optical properties of black carbon: comparison between laboratory measurements and model simulations
Characterization of tandem aerosol classifiers for selecting particles: implication for eliminating the multiple charging effect
Impact of particle size, refractive index, and shape on the determination of the particle scattering coefficient – an optical closure study evaluating different nephelometer angular truncation and illumination corrections
Quantification of major particulate matter species from a single filter type using infrared spectroscopy – application to a large-scale monitoring network
Comparing black-carbon- and aerosol-absorption-measuring instruments – a new system using lab-generated soot coated with controlled amounts of secondary organic matter
Assessment of real-time bioaerosol particle counters using reference chamber experiments
Constraining the response factors of an extractive electrospray ionization mass spectrometer for near-molecular aerosol speciation
Application of the ECT9 protocol for radiocarbon-based source apportionment of carbonaceous aerosols
Intercomparison and characterization of 23 Aethalometers under laboratory and ambient air conditions: procedures and unit-to-unit variabilities
Determination of Aethalometer multiple-scattering enhancement parameters and impact on source apportionment during the winter 2017/18 EMEP/ACTRIS/COLOSSAL campaign in Milan
Laboratory validation of a compact single-scattering albedo (SSA) monitor
Facility for production of ambient-like model aerosols (PALMA) in the laboratory: application in the intercomparison of automated PM monitors with the reference gravimetric method
An interlaboratory comparison of aerosol inorganic ion measurements by ion chromatography: implications for aerosol pH estimate
Multifactor colorimetric analysis on pH-indicator papers: an optimized approach for direct determination of ambient aerosol pH
Highly oxygenated organic molecule cluster decomposition in atmospheric pressure interface time-of-flight mass spectrometers
Mass spectral characterization of primary emissions and implications in source apportionment of organic aerosol
Nitrate radical generation via continuous generation of dinitrogen pentoxide in a laminar flow reactor coupled to an oxidation flow reactor
Development of an antioxidant assay to study oxidative potential of airborne particulate matter
Determination of n-alkanes, polycyclic aromatic hydrocarbons and hopanes in atmospheric aerosol: evaluation and comparison of thermal desorption GC-MS and solvent extraction GC-MS approaches
Inter-comparison of elemental and organic carbon mass measurements from three North American national long-term monitoring networks at a co-located site
B3010: a boosted TSI 3010 condensation particle counter for airborne studies
Effect of dry or wet substrate deposition on the organic volume fraction of core–shell aerosol particles
Spectral Intensity Bioaerosol Sensor (SIBS): an instrument for spectrally resolved fluorescence detection of single particles in real time
HOx and NOx production in oxidation flow reactors via photolysis of isopropyl nitrite, isopropyl nitrite-d7, and 1,3-propyl dinitrite at λ = 254, 350, and 369 nm
Can ozone be used to calibrate aerosol photoacoustic spectrometers?
The Fifth International Workshop on Ice Nucleation phase 2 (FIN-02): laboratory intercomparison of ice nucleation measurements
Viscosity of erythritol and erythritol–water particles as a function of water activity: new results and an intercomparison of techniques for measuring the viscosity of particles
Characterization of steady-state fluorescence properties of polystyrene latex spheres using off- and online spectroscopic methods
Organosulfates in atmospheric aerosol: synthesis and quantitative analysis of PM2.5 from Xi'an, northwestern China
Characterization of a catalyst-based conversion technique to measure total particulate nitrogen and organic carbon and comparison to a particle mass measurement instrument
On the accuracy of aerosol photoacoustic spectrometer calibrations using absorption by ozone
A reference data set for validating vapor pressure measurement techniques: homologous series of polyethylene glycols
Evaluation of the new capture vapourizer for aerosol mass spectrometers (AMS) through laboratory studies of inorganic species
Controlled nitric oxide production via O(1D) + N2O reactions for use in oxidation flow reactor studies
Characterization of three new condensation particle counters for sub-3 nm particle detection during the Helsinki CPC workshop: the ADI versatile water CPC, TSI 3777 nano enhancer and boosted TSI 3010
A novel single-cavity three-wavelength photoacoustic spectrometer for atmospheric aerosol research
Inter-comparison of NIOSH and IMPROVE protocols for OC and EC determination: implications for inter-protocol data conversion
Operation of the Airmodus A11 nano Condensation Nucleus Counter at various inlet pressures and various operation temperatures, and design of a new inlet system
The charging of neutral dimethylamine and dimethylamine–sulfuric acid clusters using protonated acetone
Validation of the poke-flow technique combined with simulations of fluid flow for determining viscosities in samples with small volumes and high viscosities
Determination of atmospheric organosulfates using HILIC chromatography with MS detection
Characterisation and optimisation of a sample preparation method for the detection and quantification of atmospherically relevant carbonyl compounds in aqueous medium
Inter-comparison of laboratory smog chamber and flow reactor systems on organic aerosol yield and composition
ECOC comparison exercise with identical thermal protocols after temperature offset correction – instrument diagnostics by in-depth evaluation of operational parameters
An intercomparison study of analytical methods used for quantification of levoglucosan in ambient aerosol filter samples
Refractory black carbon mass concentrations in snow and ice: method evaluation and inter-comparison with elemental carbon measurement
The influence of temperature calibration on the OC–EC results from a dual-optics thermal carbon analyzer
Determination of alkylamines in atmospheric aerosol particles: a comparison of gas chromatography–mass spectrometry and ion chromatography approaches
Paulus S. Bauer, Dorian Spät, Martina Eisenhut, Andreas Gattringer, and Bernadett Weinzierl
Atmos. Meas. Tech., 16, 4445–4460, https://doi.org/10.5194/amt-16-4445-2023, https://doi.org/10.5194/amt-16-4445-2023, 2023
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Particle number concentration is one of the most important parameters to quantify an aerosol. Aerosol number concentration in the nanometer range is commonly measured with condensation particle counters (CPCs). A CEN technical specification harmonizes the CPC specifications. However, it is not specified for low-pressure conditions as on high mountains or on airplanes. Here, we present the pressure-dependent performance of two different models of CEN CPCs, the Grimm 5410 CEN and the TSI 3772 CEN.
Patrick Weber, Oliver F. Bischof, Benedikt Fischer, Marcel Berg, Susanne Hering, Steven Spielman, Gregory Lewis, Andreas Petzold, and Ulrich Bundke
Atmos. Meas. Tech., 16, 3505–3514, https://doi.org/10.5194/amt-16-3505-2023, https://doi.org/10.5194/amt-16-3505-2023, 2023
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This study tests the new water condensation particle counter (MAGIC 210-LP) for deployment on passenger aircraft coordinated by the European research infrastructure IAGOS. We conducted a series of laboratory experiments for flight altitude conditions. We demonstrate that this water condensation particle counter model shows excellent agreement with a butanol-based instrument used in parallel and a Faraday cup electrometer as reference instrument at all tested pressure conditions.
Baseerat Romshoo, Mira Pöhlker, Alfred Wiedensohler, Sascha Pfeifer, Jorge Saturno, Andreas Nowak, Krzysztof Ciupek, Paul Quincey, Konstantina Vasilatou, Michaela N. Ess, Maria Gini, Konstantinos Eleftheriadis, Chris Robins, François Gaie-Levrel, and Thomas Müller
Atmos. Meas. Tech., 15, 6965–6989, https://doi.org/10.5194/amt-15-6965-2022, https://doi.org/10.5194/amt-15-6965-2022, 2022
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Black carbon (BC) is often assumed to be spherically shaped, causing uncertainties in its optical properties when modelled. This study investigates different modelling techniques for the optical properties of BC by comparing them to laboratory measurements. We provide experimental support for emphasizing the use of appropriate size representation (polydisperse size method) and morphological representation (aggregate morphology) for optical modelling and parameterization scheme development of BC.
Yao Song, Xiangyu Pei, Huichao Liu, Jiajia Zhou, and Zhibin Wang
Atmos. Meas. Tech., 15, 3513–3526, https://doi.org/10.5194/amt-15-3513-2022, https://doi.org/10.5194/amt-15-3513-2022, 2022
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Accurate particle classification is very important in aerosol studies. Differential mobility analyzers (DMAs), centrifugal particle mass analyzers (CPMAs), aerodynamic aerosol classifiers (AACs) and their tandem systems are commonly used. We demonstrated that DMA–CPMA is more susceptible to the multiple charging effect than DMA–AAC. It is not suggested to reduce the resolutions of the instruments, especially when selecting small-size soot particles.
Marilena Teri, Thomas Müller, Josef Gasteiger, Sara Valentini, Helmuth Horvath, Roberta Vecchi, Paulus Bauer, Adrian Walser, and Bernadett Weinzierl
Atmos. Meas. Tech., 15, 3161–3187, https://doi.org/10.5194/amt-15-3161-2022, https://doi.org/10.5194/amt-15-3161-2022, 2022
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We performed an extensive closure study including laboratory and simulated experiments to evaluate various angular corrections for the Aurora 4000 polar nephelometer, focusing on irregularly shaped aerosols such as mineral dust. We describe the impact of particle size, refractive index, and shape on the determination of the particle scattering coefficient and propose a guideline to establish the most appropriate angular correction depending on the aerosol type and the investigated size range.
Bruno Debus, Andrew T. Weakley, Satoshi Takahama, Kathryn M. George, Anahita Amiri-Farahani, Bret Schichtel, Scott Copeland, Anthony S. Wexler, and Ann M. Dillner
Atmos. Meas. Tech., 15, 2685–2702, https://doi.org/10.5194/amt-15-2685-2022, https://doi.org/10.5194/amt-15-2685-2022, 2022
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In the US, routine particulate matter composition is measured on samples collected on three types of filter media and analyzed using several techniques. We propose an alternate approach that uses one analytical technique, Fourier transform-infrared spectroscopy (FT-IR), and one filter type to measure the chemical composition of particulate matter in a major US monitoring network. This method could be used to add low-cost sites to the network, fill-in missing data, or for quality control.
Daniel M. Kalbermatter, Griša Močnik, Luka Drinovec, Bradley Visser, Jannis Röhrbein, Matthias Oscity, Ernest Weingartner, Antti-Pekka Hyvärinen, and Konstantina Vasilatou
Atmos. Meas. Tech., 15, 561–572, https://doi.org/10.5194/amt-15-561-2022, https://doi.org/10.5194/amt-15-561-2022, 2022
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Soot particles with varying amounts of secondary organic matter coating were generated and used to compare a series of aerosol-absorption-measuring instruments: filter-based and photoacoustic instruments as well as photo-thermal interferometers. Significant deviations in the response of the instruments were observed depending on the amount of secondary organic coating. The system can be used for the inter-comparison and characterisation of instruments.
Gian Lieberherr, Kevin Auderset, Bertrand Calpini, Bernard Clot, Benoît Crouzy, Martin Gysel-Beer, Thomas Konzelmann, José Manzano, Andrea Mihajlovic, Alireza Moallemi, David O'Connor, Branko Sikoparija, Eric Sauvageat, Fiona Tummon, and Konstantina Vasilatou
Atmos. Meas. Tech., 14, 7693–7706, https://doi.org/10.5194/amt-14-7693-2021, https://doi.org/10.5194/amt-14-7693-2021, 2021
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Today there is no standard procedure to validate bioaerosol and pollen monitors. Three instruments were tested, focusing on detecting particles of different sizes. Only one instrument was able to detect the smallest particles (0.5 µm Ø), whereas the others performed best at the largest tested particles (10 µm Ø). These results are the first step towards a standardised validation procedure. The need for a reference counting method for larger particles (pollen grains: 10–200 µm Ø) was emphasised.
Dongyu S. Wang, Chuan Ping Lee, Jordan E. Krechmer, Francesca Majluf, Yandong Tong, Manjula R. Canagaratna, Julia Schmale, André S. H. Prévôt, Urs Baltensperger, Josef Dommen, Imad El Haddad, Jay G. Slowik, and David M. Bell
Atmos. Meas. Tech., 14, 6955–6972, https://doi.org/10.5194/amt-14-6955-2021, https://doi.org/10.5194/amt-14-6955-2021, 2021
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To understand the sources and fate of particulate matter in the atmosphere, the ability to quantitatively describe its chemical composition is essential. In this work, we developed a calibration method for a state-of-the-art measurement technique without the need for chemical standards. Statistical analyses identified the driving factors behind instrument sensitivity variability towards individual components of particulate matter.
Lin Huang, Wendy Zhang, Guaciara M. Santos, Blanca T. Rodríguez, Sandra R. Holden, Vincent Vetro, and Claudia I. Czimczik
Atmos. Meas. Tech., 14, 3481–3500, https://doi.org/10.5194/amt-14-3481-2021, https://doi.org/10.5194/amt-14-3481-2021, 2021
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Radiocarbon (14C)-based source apportionment of aerosol carbon fractions requires the physical separation of OC from EC and minimizing of the incorporation of extraneous carbon. Using pure and mixed reference materials ranging in age from modern to fossil, we show that the ECT9 protocol effectively isolates OC and EC. This work expands existing opportunities for characterizing and monitoring sources of carbonaceous aerosols, including µg C-sized samples from the Arctic.
Andrea Cuesta-Mosquera, Griša Močnik, Luka Drinovec, Thomas Müller, Sascha Pfeifer, María Cruz Minguillón, Björn Briel, Paul Buckley, Vadimas Dudoitis, Javier Fernández-García, María Fernández-Amado, Joel Ferreira De Brito, Veronique Riffault, Harald Flentje, Eimear Heffernan, Nikolaos Kalivitis, Athina-Cerise Kalogridis, Hannes Keernik, Luminita Marmureanu, Krista Luoma, Angela Marinoni, Michael Pikridas, Gerhard Schauer, Norbert Serfozo, Henri Servomaa, Gloria Titos, Jesús Yus-Díez, Natalia Zioła, and Alfred Wiedensohler
Atmos. Meas. Tech., 14, 3195–3216, https://doi.org/10.5194/amt-14-3195-2021, https://doi.org/10.5194/amt-14-3195-2021, 2021
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Measurements of black carbon must be conducted with instruments operating in quality-checked and assured conditions to generate reliable and comparable data. Here, 23 Aethalometers monitoring black carbon mass concentrations in European networks were characterized and intercompared. The influence of different aerosol sources, maintenance activities, and the filter material on the instrumental variabilities were investigated. Good agreement and in general low deviations were seen.
Vera Bernardoni, Luca Ferrero, Ezio Bolzacchini, Alice Corina Forello, Asta Gregorič, Dario Massabò, Griša Močnik, Paolo Prati, Martin Rigler, Luca Santagostini, Francesca Soldan, Sara Valentini, Gianluigi Valli, and Roberta Vecchi
Atmos. Meas. Tech., 14, 2919–2940, https://doi.org/10.5194/amt-14-2919-2021, https://doi.org/10.5194/amt-14-2919-2021, 2021
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An instrument-dependent wavelength-independent parameter (C) is often used to face multiple-scattering issues affecting aerosol light absorption measurements by Aethalometers. Instead, we determined multi-wavelength C by comparison with absorption measurements of samples collected in parallel performed by an instrument developed in-house. Considering C wavelength dependence, harmonized results were obtained applying source and component apportionment models to data from different Aethalometers.
Julia Perim de Faria, Ulrich Bundke, Andrew Freedman, Timothy B. Onasch, and Andreas Petzold
Atmos. Meas. Tech., 14, 1635–1653, https://doi.org/10.5194/amt-14-1635-2021, https://doi.org/10.5194/amt-14-1635-2021, 2021
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An evaluation of the performance and accuracy of a Cavity Attenuated Phase-Shift Single Scattering Albedo Monitor (CAPS PMSSA; Aerodyne Research, Inc.) was conducted in an optical-closure study with proven technologies for aerosol particle optical-property measurements. This study demonstrates that the CAPS PMSSA is a robust and reliable instrument for the direct measurement of the particle scattering and extinction coefficients and thus single-scattering albedo.
Stefan Horender, Kevin Auderset, Paul Quincey, Stefan Seeger, Søren Nielsen Skov, Kai Dirscherl, Thomas O. M. Smith, Katie Williams, Camille C. Aegerter, Daniel M. Kalbermatter, François Gaie-Levrel, and Konstantina Vasilatou
Atmos. Meas. Tech., 14, 1225–1238, https://doi.org/10.5194/amt-14-1225-2021, https://doi.org/10.5194/amt-14-1225-2021, 2021
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A new facility has been developed which allows for the stable and reproducible generation of ambient-like model aerosols in the laboratory. The set-up consists of multiple aerosol generators, a custom-made flow tube homogeniser, isokinetic sampling probes, and a system to control aerosol temperature and humidity. The model aerosols, which contain fresh and aged soot, inorganic salt, and dust particles, can be used for the calibration of air quality monitoring instruments.
Jingsha Xu, Shaojie Song, Roy M. Harrison, Congbo Song, Lianfang Wei, Qiang Zhang, Yele Sun, Lu Lei, Chao Zhang, Xiaohong Yao, Dihui Chen, Weijun Li, Miaomiao Wu, Hezhong Tian, Lining Luo, Shengrui Tong, Weiran Li, Junling Wang, Guoliang Shi, Yanqi Huangfu, Yingze Tian, Baozhu Ge, Shaoli Su, Chao Peng, Yang Chen, Fumo Yang, Aleksandra Mihajlidi-Zelić, Dragana Đorđević, Stefan J. Swift, Imogen Andrews, Jacqueline F. Hamilton, Ye Sun, Agung Kramawijaya, Jinxiu Han, Supattarachai Saksakulkrai, Clarissa Baldo, Siqi Hou, Feixue Zheng, Kaspar R. Daellenbach, Chao Yan, Yongchun Liu, Markku Kulmala, Pingqing Fu, and Zongbo Shi
Atmos. Meas. Tech., 13, 6325–6341, https://doi.org/10.5194/amt-13-6325-2020, https://doi.org/10.5194/amt-13-6325-2020, 2020
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An interlaboratory comparison was conducted for the first time to examine differences in water-soluble inorganic ions (WSIIs) measured by 10 labs using ion chromatography (IC) and by two online aerosol chemical speciation monitor (ACSM) methods. Major ions including SO42−, NO3− and NH4+ agreed well in 10 IC labs and correlated well with ACSM data. WSII interlab variability strongly affected aerosol acidity results based on ion balance, but aerosol pH computed by ISORROPIA II was very similar.
Guo Li, Hang Su, Nan Ma, Guangjie Zheng, Uwe Kuhn, Meng Li, Thomas Klimach, Ulrich Pöschl, and Yafang Cheng
Atmos. Meas. Tech., 13, 6053–6065, https://doi.org/10.5194/amt-13-6053-2020, https://doi.org/10.5194/amt-13-6053-2020, 2020
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Aerosol acidity plays an important role in regulating the chemistry, health, and ecological effect of aerosol particles. However, a direct measurement of aerosol pH is very challenging because of its fast transition and equilibrium with adjacent environments. Therefore, most early studies have to use modeled pH, resulting in intensive debates about model uncertainties. Here we developed an optimized approach to measure aerosol pH by using pH-indicator papers combined with RGB-based colorimetry.
Tommaso Zanca, Jakub Kubečka, Evgeni Zapadinsky, Monica Passananti, Theo Kurtén, and Hanna Vehkamäki
Atmos. Meas. Tech., 13, 3581–3593, https://doi.org/10.5194/amt-13-3581-2020, https://doi.org/10.5194/amt-13-3581-2020, 2020
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In this paper we quantify (using a statistical model) the probability of decomposition of a representative class of HOM clusters in an APi-TOF mass spectrometer. This is important because it quantifies the systematic error of measurements in a APi-TOF MS due to cluster decomposition. The results (specific for our selected clusters) show that decomposition is negligible, provided their bonding energy is large enough to allow formation in the atmosphere in the first place.
Weiqi Xu, Yao He, Yanmei Qiu, Chun Chen, Conghui Xie, Lu Lei, Zhijie Li, Jiaxing Sun, Junyao Li, Pingqing Fu, Zifa Wang, Douglas R. Worsnop, and Yele Sun
Atmos. Meas. Tech., 13, 3205–3219, https://doi.org/10.5194/amt-13-3205-2020, https://doi.org/10.5194/amt-13-3205-2020, 2020
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We characterized mass spectral features of organic aerosol (OA) and water-soluble OA (WSOA) from 21 cooking, crop straw, wood, and coal burning experiments using aerosol mass spectrometers with standard and capture vaporizers, and we demonstrated the applications of source spectral profiles in improving source apportionment of ambient OA at a highly polluted rural site in the North China Plain in winter.
Andrew T. Lambe, Ezra C. Wood, Jordan E. Krechmer, Francesca Majluf, Leah R. Williams, Philip L. Croteau, Manuela Cirtog, Anaïs Féron, Jean-Eudes Petit, Alexandre Albinet, Jose L. Jimenez, and Zhe Peng
Atmos. Meas. Tech., 13, 2397–2411, https://doi.org/10.5194/amt-13-2397-2020, https://doi.org/10.5194/amt-13-2397-2020, 2020
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We present a new method to continuously generate N2O5 in the gas phase that is injected into a reactor where it decomposes to generate nitrate radicals (NO3). To assess the applicability of the method towards different chemical systems, we present experimental and model characterization of the integrated NO3 exposure and other metrics as a function of operating conditions. We demonstrate the method by characterizing secondary organic aerosol particles generated from the β-pinene + NO3 reaction.
Pourya Shahpoury, Tom Harner, Gerhard Lammel, Steven Lelieveld, Haijie Tong, and Jake Wilson
Atmos. Meas. Tech., 12, 6529–6539, https://doi.org/10.5194/amt-12-6529-2019, https://doi.org/10.5194/amt-12-6529-2019, 2019
Meng Wang, Ru-Jin Huang, Junji Cao, Wenting Dai, Jiamao Zhou, Chunshui Lin, Haiyan Ni, Jing Duan, Ting Wang, Yang Chen, Yongjie Li, Qi Chen, Imad El Haddad, and Thorsten Hoffmann
Atmos. Meas. Tech., 12, 4779–4789, https://doi.org/10.5194/amt-12-4779-2019, https://doi.org/10.5194/amt-12-4779-2019, 2019
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The analytical performances of SE-GC-MS and TD-GC-MS for the determination of n-alkanes, PAHs and hopanes were evaluated and compared. The two methods show a good agreement with a high correlation efficient (R2 > 0.98) and a slope close to unity. The concentrations of n-alkanes, PAHs and hopanes are found to be much higher in Beijing than those in Chengdu, Shanghai and Guangzhou, most likely due to emissions from coal combustion for wintertime heating in Beijing.
Tak W. Chan, Lin Huang, Kulbir Banwait, Wendy Zhang, Darrell Ernst, Xiaoliang Wang, John G. Watson, Judith C. Chow, Mark Green, Claudia I. Czimczik, Guaciara M. Santos, Sangeeta Sharma, and Keith Jones
Atmos. Meas. Tech., 12, 4543–4560, https://doi.org/10.5194/amt-12-4543-2019, https://doi.org/10.5194/amt-12-4543-2019, 2019
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This study compared 10 years of carbonaceous aerosol measurements collected at Egbert by three North American long-term monitoring networks. The study evaluated how differences in sample collection and analysis affected the concentrations of total carbon (TC), organic carbon (OC), and elemental carbon (EC). Various carbonaceous fractions measured by the three networks were consistent and comparable over the period. Elevated OC and EC were observed when ambient temperature exceeded 10 °C.
David Picard, Michel Attoui, and Karine Sellegri
Atmos. Meas. Tech., 12, 2531–2543, https://doi.org/10.5194/amt-12-2531-2019, https://doi.org/10.5194/amt-12-2531-2019, 2019
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We report here how we managed to improve the performance of an aerosol particle counter model TSI3010. Our device is based on a secondhand unit and reuses its core elements (saturator, condenser, optics). We redesigned the electronics and thermal management. Laboratory experiments show that the cutoff diameter was decreased from 10 to 2.5 nm, bringing the B3010 close to more complex and expensive products. These results may help designers and users improve the performance of their devices.
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
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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.
Tobias Könemann, Nicole Savage, Thomas Klimach, David Walter, Janine Fröhlich-Nowoisky, Hang Su, Ulrich Pöschl, J. Alex Huffman, and Christopher Pöhlker
Atmos. Meas. Tech., 12, 1337–1363, https://doi.org/10.5194/amt-12-1337-2019, https://doi.org/10.5194/amt-12-1337-2019, 2019
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This study presents a comprehensive assessment of the SIBS, an instrument for spectrally resolved fluorescence detection of single particles. Exemplary ambient data and fluorescence spectra obtained for 16 reference compounds (biofluorophores and PSLs) show that the SIBS has the ability to expand the scope of fluorescent bioaerosol quantification and classification. Detailed technical insights will be broadly beneficial for users of various WIBS generations and other LIF instruments.
Andrew T. Lambe, Jordan E. Krechmer, Zhe Peng, Jason R. Casar, Anthony J. Carrasquillo, Jonathan D. Raff, Jose L. Jimenez, and Douglas R. Worsnop
Atmos. Meas. Tech., 12, 299–311, https://doi.org/10.5194/amt-12-299-2019, https://doi.org/10.5194/amt-12-299-2019, 2019
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This paper is an evaluation of methods used to generate OH radicals under conditions with high concentrations of NO and NO2 to simulate oxidation chemistry in polluted urban atmospheres over equivalent atmospheric timescales of ~ 1 day.
D. Al Fischer and Geoffrey D. Smith
Atmos. Meas. Tech., 11, 6419–6427, https://doi.org/10.5194/amt-11-6419-2018, https://doi.org/10.5194/amt-11-6419-2018, 2018
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Photoacoustic spectroscopy is a commonly used technique for measuring light absorption by aerosols, but it requires careful calibration to be accurate. Here, we explore the use of one popular calibrant, ozone, and demonstrate that its response is dependent on the identity of the bath gas used.
Paul J. DeMott, Ottmar Möhler, Daniel J. Cziczo, Naruki Hiranuma, Markus D. Petters, Sarah S. Petters, Franco Belosi, Heinz G. Bingemer, Sarah D. Brooks, Carsten Budke, Monika Burkert-Kohn, Kristen N. Collier, Anja Danielczok, Oliver Eppers, Laura Felgitsch, Sarvesh Garimella, Hinrich Grothe, Paul Herenz, Thomas C. J. Hill, Kristina Höhler, Zamin A. Kanji, Alexei Kiselev, Thomas Koop, Thomas B. Kristensen, Konstantin Krüger, Gourihar Kulkarni, Ezra J. T. Levin, Benjamin J. Murray, Alessia Nicosia, Daniel O'Sullivan, Andreas Peckhaus, Michael J. Polen, Hannah C. Price, Naama Reicher, Daniel A. Rothenberg, Yinon Rudich, Gianni Santachiara, Thea Schiebel, Jann Schrod, Teresa M. Seifried, Frank Stratmann, Ryan C. Sullivan, Kaitlyn J. Suski, Miklós Szakáll, Hans P. Taylor, Romy Ullrich, Jesus Vergara-Temprado, Robert Wagner, Thomas F. Whale, Daniel Weber, André Welti, Theodore W. Wilson, Martin J. Wolf, and Jake Zenker
Atmos. Meas. Tech., 11, 6231–6257, https://doi.org/10.5194/amt-11-6231-2018, https://doi.org/10.5194/amt-11-6231-2018, 2018
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The ability to measure ice nucleating particles is vital to quantifying their role in affecting clouds and precipitation. Methods for measuring droplet freezing were compared while co-sampling relevant particle types. Measurement correspondence was very good for ice nucleating particles of bacterial and natural soil origin, and somewhat more disparate for those of mineral origin. Results reflect recently improved capabilities and provide direction toward addressing remaining measurement issues.
Yangxi Chu, Erin Evoy, Saeid Kamal, Young Chul Song, Jonathan P. Reid, Chak K. Chan, and Allan K. Bertram
Atmos. Meas. Tech., 11, 4809–4822, https://doi.org/10.5194/amt-11-4809-2018, https://doi.org/10.5194/amt-11-4809-2018, 2018
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The viscosity of erythritol, a tetrol found in aerosol particles, is highly uncertain. To help resolve this uncertainty, we measured the viscosities of
erythritol–water particles using rectangular-area fluorescence recovery after photobleaching and aerosol optical tweezers techniques. These results
should help improve the understanding of the viscosity of secondary organic aerosol particles. In addition, we present an intercomparison of techniques
for measuring the viscosity of particles.
Tobias Könemann, Nicole J. Savage, J. Alex Huffman, and Christopher Pöhlker
Atmos. Meas. Tech., 11, 3987–4003, https://doi.org/10.5194/amt-11-3987-2018, https://doi.org/10.5194/amt-11-3987-2018, 2018
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This study presents an overview of fluorescence properties of polystyrene latex spheres (PSLs), which are widely used in numerous scientific disciplines. By using different spectroscopic techniques, we show that the
fluorescence landscapeof PSLs is more complex than the information provided by manufacturers may imply. By understanding general fluorescence properties of PSLs, individual researchers may probe specific spectral features important to the operation of their own instruments.
Ru-Jin Huang, Junji Cao, Yang Chen, Lu Yang, Jincan Shen, Qihua You, Kai Wang, Chunshui Lin, Wei Xu, Bo Gao, Yongjie Li, Qi Chen, Thorsten Hoffmann, Colin D. O'Dowd, Merete Bilde, and Marianne Glasius
Atmos. Meas. Tech., 11, 3447–3456, https://doi.org/10.5194/amt-11-3447-2018, https://doi.org/10.5194/amt-11-3447-2018, 2018
Chelsea E. Stockwell, Agnieszka Kupc, Bartłomiej Witkowski, Ranajit K. Talukdar, Yong Liu, Vanessa Selimovic, Kyle J. Zarzana, Kanako Sekimoto, Carsten Warneke, Rebecca A. Washenfelder, Robert J. Yokelson, Ann M. Middlebrook, and James M. Roberts
Atmos. Meas. Tech., 11, 2749–2768, https://doi.org/10.5194/amt-11-2749-2018, https://doi.org/10.5194/amt-11-2749-2018, 2018
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This work investigates the total conversion of particle-bound nitrogen and organic carbon across platinum and molybdenum catalysts followed by NO–O3 chemiluminescence and nondispersive infrared CO2 detection. We show the instrument is an accurate particle mass measurement method and demonstrate its ability to calibrate particle mass measurement instrumentation through comparisons with a calibrated particle-into-liquid sampler coupled to an electrospray ionization source of a mass spectrometer.
Nicholas W. Davies, Michael I. Cotterell, Cathryn Fox, Kate Szpek, Jim M. Haywood, and Justin M. Langridge
Atmos. Meas. Tech., 11, 2313–2324, https://doi.org/10.5194/amt-11-2313-2018, https://doi.org/10.5194/amt-11-2313-2018, 2018
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The poorly characterised optical properties of atmospheric aerosols are one of the major uncertainties when modelling future climate change. Photoacoustic spectroscopy is an accurate and sensitive method for measurement of aerosol light absorption. Photoacoustic spectrometers require calibration; hence this study validates the use of ozone as a calibrant and simultaneously verifies the accuracy of the photoacoustic spectrometers in question.
Ulrich K. Krieger, Franziska Siegrist, Claudia Marcolli, Eva U. Emanuelsson, Freya M. Gøbel, Merete Bilde, Aleksandra Marsh, Jonathan P. Reid, Andrew J. Huisman, Ilona Riipinen, Noora Hyttinen, Nanna Myllys, Theo Kurtén, Thomas Bannan, Carl J. Percival, and David Topping
Atmos. Meas. Tech., 11, 49–63, https://doi.org/10.5194/amt-11-49-2018, https://doi.org/10.5194/amt-11-49-2018, 2018
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Vapor pressures of low-volatility organic molecules at atmospheric temperatures reported in the literature often differ by several orders of magnitude between measurement techniques. These discrepancies exceed the stated uncertainty of each technique, which is generally reported to be smaller than a factor of 2. We determined saturation vapor pressures for the homologous series of polyethylene glycols ranging in vapor pressure at 298 K from 1E−7 Pa to 5E−2 Pa as a reference set.
Weiwei Hu, Pedro Campuzano-Jost, Douglas A. Day, Philip Croteau, Manjula R. Canagaratna, John T. Jayne, Douglas R. Worsnop, and Jose L. Jimenez
Atmos. Meas. Tech., 10, 2897–2921, https://doi.org/10.5194/amt-10-2897-2017, https://doi.org/10.5194/amt-10-2897-2017, 2017
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Aerosol mass spectrometers (AMS) from ARI are used widely to measure the non-refractory species in PM1. Recently, a new capture vapourizer (CV) has been designed to reduce the need for a bounce-related CE correction in the commonly used standard vapourizer (SV) installed in AMS. To test the CV, the fragments, CE and size distributions of four pure inorganic species in the CV-AMS are investigated in various laboratory experiments. Results from the co-located SV-AMS are also shown as a comparison.
Andrew Lambe, Paola Massoli, Xuan Zhang, Manjula Canagaratna, John Nowak, Conner Daube, Chao Yan, Wei Nie, Timothy Onasch, John Jayne, Charles Kolb, Paul Davidovits, Douglas Worsnop, and William Brune
Atmos. Meas. Tech., 10, 2283–2298, https://doi.org/10.5194/amt-10-2283-2017, https://doi.org/10.5194/amt-10-2283-2017, 2017
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This work enables the study of NOx-influenced secondary organic aerosol formation chemistry in oxidation flow reactors to an extent that was not previously possible. The method uses reactions of exited oxygen O(1D) radicals (formed from ozone photolysis at 254 nm or nitrous oxide photolysis at 185 nm) with nitrous oxide (N2O) to produce NO. We demonstrate proof of concept using chemical ionization mass spectrometer measurements to detect gas-phase oxidation products of isoprene and α -pinene.
Juha Kangasluoma, Susanne Hering, David Picard, Gregory Lewis, Joonas Enroth, Frans Korhonen, Markku Kulmala, Karine Sellegri, Michel Attoui, and Tuukka Petäjä
Atmos. Meas. Tech., 10, 2271–2281, https://doi.org/10.5194/amt-10-2271-2017, https://doi.org/10.5194/amt-10-2271-2017, 2017
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The manuscript presents a characterization of three new particle counters able to detect airborne nanoparticles smaller than 3 nm in diameter. We explored some of the parameters affecting the smallest detectable particle size, such as sample flow relative humidity, the particle chemical composition and the electrical charging state. The characterization results help one to select a suitable particle counter for a given application.
Claudia Linke, Inas Ibrahim, Nina Schleicher, Regina Hitzenberger, Meinrat O. Andreae, Thomas Leisner, and Martin Schnaiter
Atmos. Meas. Tech., 9, 5331–5346, https://doi.org/10.5194/amt-9-5331-2016, https://doi.org/10.5194/amt-9-5331-2016, 2016
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Various carbonaceous materials are present in the atmosphere. Besides gaseous organic compounds, carbonaceous particles like soot are emitted into the air from traffic sources, residential wood combustion, or wildfires. Variable chemical compositions of such materials, which often result from incomplete combustion processes, show differences in the absorption behavior at visible wavelengths. Our instrument is able to measure the absorption at three visible wavelengths.
Cheng Wu, X. H. Hilda Huang, Wai Man Ng, Stephen M. Griffith, and Jian Zhen Yu
Atmos. Meas. Tech., 9, 4547–4560, https://doi.org/10.5194/amt-9-4547-2016, https://doi.org/10.5194/amt-9-4547-2016, 2016
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Organic carbon (OC) and elemental carbon (EC) in more than 1300 Hong Kong samples were analyzed using both NIOSH TOT and IMPROVE TOR protocols. EC discrepancy between the two protocols mainly (83 %) arises from a difference in peak inert mode temperature, while the rest (17 %) is attributed to a difference in the optical method (transmittance vs. reflectance) applied for the charring correction. Two approaches are proposed to translate NIOSH TOT OC and EC data into IMPROVE TOR OC and EC data.
Juha Kangasluoma, Alessandro Franchin, Jonahtan Duplissy, Lauri Ahonen, Frans Korhonen, Michel Attoui, Jyri Mikkilä, Katrianne Lehtipalo, Joonas Vanhanen, Markku Kulmala, and Tuukka Petäjä
Atmos. Meas. Tech., 9, 2977–2988, https://doi.org/10.5194/amt-9-2977-2016, https://doi.org/10.5194/amt-9-2977-2016, 2016
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The paper describes technical aspects of using the Airmodus A11 nCNC at various inlet pressures and how temperature selection affects the performance of the instrument. We also present a sampling box to minimize the inlet losses and make use of the instrument more convenient.
K. Ruusuvuori, P. Hietala, O. Kupiainen-Määttä, T. Jokinen, H. Junninen, M. Sipilä, T. Kurtén, and H. Vehkamäki
Atmos. Meas. Tech., 8, 2577–2588, https://doi.org/10.5194/amt-8-2577-2015, https://doi.org/10.5194/amt-8-2577-2015, 2015
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Ionization reagents suitable for accurate measurements of the atmospheric gas-phase amine vapour concentrations are needed. Based on computational results, acetone is a viable option for use as an ionization reagent in CI-APi-TOF measurements on atmospheric dimethylamine. However, comparison between the computational and experimental results revealed notable discrepancies. Further study is still required before the acetone CI-APi-TOF can be considered a viable option in practice.
J. W. Grayson, M. Song, M. Sellier, and A. K. Bertram
Atmos. Meas. Tech., 8, 2463–2472, https://doi.org/10.5194/amt-8-2463-2015, https://doi.org/10.5194/amt-8-2463-2015, 2015
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
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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.
M. Rodigast, A. Mutzel, Y. Iinuma, S. Haferkorn, and H. Herrmann
Atmos. Meas. Tech., 8, 2409–2416, https://doi.org/10.5194/amt-8-2409-2015, https://doi.org/10.5194/amt-8-2409-2015, 2015
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An optimised method for derivatisation of carbonyl compounds with o-(2,3,4,5,6-pentafluorobenzyl)hydroxylamine (PFBHA) in aqueous samples is described. The comprehensive optimisation of the method leads to an improvement of the detection limit up to a factor of 10 highlighting the good sensitivity of the optimised method for atmospherically relevant carbonyl compounds. The optimised method was successfully applied to detect carbonyl compounds from the aqueous phase oxidation of 3-methylbutanone.
E. A. Bruns, I. El Haddad, A. Keller, F. Klein, N. K. Kumar, S. M. Pieber, J. C. Corbin, J. G. Slowik, W. H. Brune, U. Baltensperger, and A. S. H. Prévôt
Atmos. Meas. Tech., 8, 2315–2332, https://doi.org/10.5194/amt-8-2315-2015, https://doi.org/10.5194/amt-8-2315-2015, 2015
P. Panteliadis, T. Hafkenscheid, B. Cary, E. Diapouli, A. Fischer, O. Favez, P. Quincey, M. Viana, R. Hitzenberger, R. Vecchi, D. Saraga, J. Sciare, J. L. Jaffrezo, A. John, J. Schwarz, M. Giannoni, J. Novak, A. Karanasiou, P. Fermo, and W. Maenhaut
Atmos. Meas. Tech., 8, 779–792, https://doi.org/10.5194/amt-8-779-2015, https://doi.org/10.5194/amt-8-779-2015, 2015
K. E. Yttri, J. Schnelle-Kreis, W. Maenhaut, G. Abbaszade, C. Alves, A. Bjerke, N. Bonnier, R. Bossi, M. Claeys, C. Dye, M. Evtyugina, D. García-Gacio, R. Hillamo, A. Hoffer, M. Hyder, Y. Iinuma, J.-L. Jaffrezo, A. Kasper-Giebl, G. Kiss, P. L. López-Mahia, C. Pio, C. Piot, C. Ramirez-Santa-Cruz, J. Sciare, K. Teinilä, R. Vermeylen, A. Vicente, and R. Zimmermann
Atmos. Meas. Tech., 8, 125–147, https://doi.org/10.5194/amt-8-125-2015, https://doi.org/10.5194/amt-8-125-2015, 2015
S. Lim, X. Faïn, M. Zanatta, J. Cozic, J.-L. Jaffrezo, P. Ginot, and P. Laj
Atmos. Meas. Tech., 7, 3307–3324, https://doi.org/10.5194/amt-7-3307-2014, https://doi.org/10.5194/amt-7-3307-2014, 2014
J. Pavlovic, J. S. Kinsey, and M. D. Hays
Atmos. Meas. Tech., 7, 2829–2838, https://doi.org/10.5194/amt-7-2829-2014, https://doi.org/10.5194/amt-7-2829-2014, 2014
R.-J. Huang, W.-B. Li, Y.-R. Wang, Q. Y. Wang, W. T. Jia, K.-F. Ho, J. J. Cao, G. H. Wang, X. Chen, I. EI Haddad, Z. X. Zhuang, X. R. Wang, A. S. H. Prévôt, C. D. O'Dowd, and T. Hoffmann
Atmos. Meas. Tech., 7, 2027–2035, https://doi.org/10.5194/amt-7-2027-2014, https://doi.org/10.5194/amt-7-2027-2014, 2014
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Short summary
We describe a stepwise uncertainty analysis of 14C measurements of organic (OC) and elemental (EC) carbon fractions of aerosols. Using the Swiss_4S thermal-optical protocol with a newly established trapping setup, we show that we can efficiently isolate and trap each carbon fraction and perform 14C analysis of ultra-small OC and EC samples with high accuracy and low 14C blanks. Our study presents a first step towards the development of a common protocol for OC and EC 14C measurements.
We describe a stepwise uncertainty analysis of 14C measurements of organic (OC) and elemental...
