Articles | Volume 19, issue 11
https://doi.org/10.5194/acp-19-7817-2019
© Author(s) 2019. 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-19-7817-2019
© Author(s) 2019. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Research article
| 
12 Jun 2019
Research article |
| 12 Jun 2019
| 12 Jun 2019
Seasonal features and origins of carbonaceous aerosols at Syowa Station, coastal Antarctica
Department of Earth System Science, Faculty of Science, Fukuoka University, Fukuoka, 814-0180, Japan
Kengo Sudo
Graduate School of Environmental Studies, Nagoya University, Nagoya, 464-8601, Japan
Takato Ohnishi
Graduate School of Environmental Studies, Nagoya University, Nagoya, 464-8601, Japan
Kazuo Osada
Graduate School of Environmental Studies, Nagoya University, Nagoya, 464-8601, Japan
Masanori Yabuki
Research Institute for Sustainable Humanosphere, Kyoto University, Kyoto, 611-0011, Japan
Masataka Shiobara
National Institute of Polar Research, Tokyo, 190-0014, Japan
Takashi Yamanouchi
National Institute of Polar Research, Tokyo, 190-0014, Japan
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Kazuyuki Miyazaki, Kevin W. Bowman, Keiya Yumimoto, Thomas Walker, and Kengo Sudo
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Lei Kong, Xiao Tang, Jiang Zhu, Zifa Wang, Joshua S. Fu, Xuemei Wang, Syuichi Itahashi, Kazuyo Yamaji, Tatsuya Nagashima, Hyo-Jung Lee, Cheol-Hee Kim, Chuan-Yao Lin, Lei Chen, Meigen Zhang, Zhining Tao, Jie Li, Mizuo Kajino, Hong Liao, Zhe Wang, Kengo Sudo, Yuesi Wang, Yuepeng Pan, Guiqian Tang, Meng Li, Qizhong Wu, Baozhu Ge, and Gregory R. Carmichael
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Akihiro Uchiyama, Masataka Shiobara, Hiroshi Kobayashi, Tsuneo Matsunaga, Akihiro Yamazaki, Kazunori Inei, Kazuhiro Kawai, and Yoshiaki Watanabe
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Geosci. Model Dev., 12, 2727–2765, https://doi.org/10.5194/gmd-12-2727-2019, https://doi.org/10.5194/gmd-12-2727-2019, 2019
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Yugo Kanaya, Kazuyuki Miyazaki, Fumikazu Taketani, Takuma Miyakawa, Hisahiro Takashima, Yuichi Komazaki, Xiaole Pan, Saki Kato, Kengo Sudo, Takashi Sekiya, Jun Inoue, Kazutoshi Sato, and Kazuhiro Oshima
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Zainab Q. Hakim, Scott Archer-Nicholls, Gufran Beig, Gerd A. Folberth, Kengo Sudo, Nathan Luke Abraham, Sachin Ghude, Daven K. Henze, and Alexander T. Archibald
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Kai-Lan Chang, Owen R. Cooper, J. Jason West, Marc L. Serre, Martin G. Schultz, Meiyun Lin, Virginie Marécal, Béatrice Josse, Makoto Deushi, Kengo Sudo, Junhua Liu, and Christoph A. Keller
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Jan Eiof Jonson, Michael Schulz, Louisa Emmons, Johannes Flemming, Daven Henze, Kengo Sudo, Marianne Tronstad Lund, Meiyun Lin, Anna Benedictow, Brigitte Koffi, Frank Dentener, Terry Keating, Rigel Kivi, and Yanko Davila
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Focusing on Europe, this HTAP 2 study computes ozone in several global models when reducing anthropogenic emissions by 20 % in different world regions. The differences in model results are explored
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Pakawat Phalitnonkiat, Peter G. M. Hess, Mircea D. Grigoriu, Gennady Samorodnitsky, Wenxiu Sun, Ellie Beaudry, Simone Tilmes, Makato Deushi, Beatrice Josse, David Plummer, and Kengo Sudo
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Ciao-Kai Liang, J. Jason West, Raquel A. Silva, Huisheng Bian, Mian Chin, Yanko Davila, Frank J. Dentener, Louisa Emmons, Johannes Flemming, Gerd Folberth, Daven Henze, Ulas Im, Jan Eiof Jonson, Terry J. Keating, Tom Kucsera, Allen Lenzen, Meiyun Lin, Marianne Tronstad Lund, Xiaohua Pan, Rokjin J. Park, R. Bradley Pierce, Takashi Sekiya, Kengo Sudo, and Toshihiko Takemura
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We investigated mixing states and morphological features of soot-containing particles, by using water-dialysis analysis in remote ocean areas over the southern Indian Ocean and the Southern Ocean. Most particles were water-soluble. However, rarely were particles (2.1 % of particles on a TEM sample at a maximum) found to contain insoluble residuals with the characteristic soot shape.
Stefano Galmarini, Ioannis Kioutsioukis, Efisio Solazzo, Ummugulsum Alyuz, Alessandra Balzarini, Roberto Bellasio, Anna M. K. Benedictow, Roberto Bianconi, Johannes Bieser, Joergen Brandt, Jesper H. Christensen, Augustin Colette, Gabriele Curci, Yanko Davila, Xinyi Dong, Johannes Flemming, Xavier Francis, Andrea Fraser, Joshua Fu, Daven K. Henze, Christian Hogrefe, Ulas Im, Marta Garcia Vivanco, Pedro Jiménez-Guerrero, Jan Eiof Jonson, Nutthida Kitwiroon, Astrid Manders, Rohit Mathur, Laura Palacios-Peña, Guido Pirovano, Luca Pozzoli, Marie Prank, Martin Schultz, Rajeet S. Sokhi, Kengo Sudo, Paolo Tuccella, Toshihiko Takemura, Takashi Sekiya, and Alper Unal
Atmos. Chem. Phys., 18, 8727–8744, https://doi.org/10.5194/acp-18-8727-2018, https://doi.org/10.5194/acp-18-8727-2018, 2018
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An ensemble of model results relating to ozone concentrations in Europe in 2010 has been produced and studied. The novelty consists in the fact that the ensemble is made of results of models working at two different scales (regional and global), therefore contributing in detail two different parts of the atmospheric spectrum. The ensemble defined as a hybrid has been studied in detail and shown to bring additional value to the assessment of air quality.
Sandip S. Dhomse, Douglas Kinnison, Martyn P. Chipperfield, Ross J. Salawitch, Irene Cionni, Michaela I. Hegglin, N. Luke Abraham, Hideharu Akiyoshi, Alex T. Archibald, Ewa M. Bednarz, Slimane Bekki, Peter Braesicke, Neal Butchart, Martin Dameris, Makoto Deushi, Stacey Frith, Steven C. Hardiman, Birgit Hassler, Larry W. Horowitz, Rong-Ming Hu, Patrick Jöckel, Beatrice Josse, Oliver Kirner, Stefanie Kremser, Ulrike Langematz, Jared Lewis, Marion Marchand, Meiyun Lin, Eva Mancini, Virginie Marécal, Martine Michou, Olaf Morgenstern, Fiona M. O'Connor, Luke Oman, Giovanni Pitari, David A. Plummer, John A. Pyle, Laura E. Revell, Eugene Rozanov, Robyn Schofield, Andrea Stenke, Kane Stone, Kengo Sudo, Simone Tilmes, Daniele Visioni, Yousuke Yamashita, and Guang Zeng
Atmos. Chem. Phys., 18, 8409–8438, https://doi.org/10.5194/acp-18-8409-2018, https://doi.org/10.5194/acp-18-8409-2018, 2018
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We analyse simulations from the Chemistry-Climate Model Initiative (CCMI) to estimate the return dates of the stratospheric ozone layer from depletion by anthropogenic chlorine and bromine. The simulations from 20 models project that global column ozone will return to 1980 values in 2047 (uncertainty range 2042–2052). Return dates in other regions vary depending on factors related to climate change and importance of chlorine and bromine. Column ozone in the tropics may continue to decline.
Jiani Tan, Joshua S. Fu, Frank Dentener, Jian Sun, Louisa Emmons, Simone Tilmes, Kengo Sudo, Johannes Flemming, Jan Eiof Jonson, Sylvie Gravel, Huisheng Bian, Yanko Davila, Daven K. Henze, Marianne T. Lund, Tom Kucsera, Toshihiko Takemura, and Terry Keating
Atmos. Chem. Phys., 18, 6847–6866, https://doi.org/10.5194/acp-18-6847-2018, https://doi.org/10.5194/acp-18-6847-2018, 2018
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We study the distributions of sulfur and nitrogen deposition, which are associated with current environmental issues such as formation of acid rain and ecosystem eutrophication and result in widespread problems such as loss of environmental diversity, harming the crop yield and even food insecurity. According to our study, both the amount and distribution of sulfate and nitrogen deposition have changed significantly in the last decade, particularly in East Asia, South Asia and Southeast Asia.
Takashi Sekiya, Kazuyuki Miyazaki, Koji Ogochi, Kengo Sudo, and Masayuki Takigawa
Geosci. Model Dev., 11, 959–988, https://doi.org/10.5194/gmd-11-959-2018, https://doi.org/10.5194/gmd-11-959-2018, 2018
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We evaluate global tropospheric NO2 simulations using a chemical transport model (CTM) at horizontal resolutions of 0.56, 1.1, and 2.8°. Agreement against satellite retrievals improved greatly at 0.56 and 1.1° resolutions (compared to 2.8°) over polluted and biomass burning regions, especially over areas with strong local sources, such as a megacity. The evaluations demonstrate the potential of using a high-resolution global CTM for studying megacity-scale air pollutants across the entire globe.
Olaf Morgenstern, Kane A. Stone, Robyn Schofield, Hideharu Akiyoshi, Yousuke Yamashita, Douglas E. Kinnison, Rolando R. Garcia, Kengo Sudo, David A. Plummer, John Scinocca, Luke D. Oman, Michael E. Manyin, Guang Zeng, Eugene Rozanov, Andrea Stenke, Laura E. Revell, Giovanni Pitari, Eva Mancini, Glauco Di Genova, Daniele Visioni, Sandip S. Dhomse, and Martyn P. Chipperfield
Atmos. Chem. Phys., 18, 1091–1114, https://doi.org/10.5194/acp-18-1091-2018, https://doi.org/10.5194/acp-18-1091-2018, 2018
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We assess how ozone as simulated by a group of chemistry–climate models responds to variations in man-made climate gases and ozone-depleting substances. We find some agreement, particularly in the middle and upper stratosphere, but also considerable disagreement elsewhere. Such disagreement affects the reliability of future ozone projections based on these models, and also constitutes a source of uncertainty in climate projections using prescribed ozone derived from these simulations.
Itsushi Uno, Kazuo Osada, Keiya Yumimoto, Zhe Wang, Syuichi Itahashi, Xiaole Pan, Yukari Hara, Yugo Kanaya, Shigekazu Yamamoto, and Thomas Duncan Fairlie
Atmos. Chem. Phys., 17, 14181–14197, https://doi.org/10.5194/acp-17-14181-2017, https://doi.org/10.5194/acp-17-14181-2017, 2017
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We analyzed long-term fine- and coarse-mode nitrate and related aerosols synergetic observations at Fukuoka, Japan. GEOS Chem model including dust and sea-salt acid uptake processes was used to assess the observed seasonal variation, and the impact of long-range transport from the Asian continent. A numerical model reproduced the seasonal variations of fine aerosols. For coarse nitrate, large-scale dust-nitrate outflow from China was confirmed during all dust events between January and June.
Huisheng Bian, Mian Chin, Didier A. Hauglustaine, Michael Schulz, Gunnar Myhre, Susanne E. Bauer, Marianne T. Lund, Vlassis A. Karydis, Tom L. Kucsera, Xiaohua Pan, Andrea Pozzer, Ragnhild B. Skeie, Stephen D. Steenrod, Kengo Sudo, Kostas Tsigaridis, Alexandra P. Tsimpidi, and Svetlana G. Tsyro
Atmos. Chem. Phys., 17, 12911–12940, https://doi.org/10.5194/acp-17-12911-2017, https://doi.org/10.5194/acp-17-12911-2017, 2017
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Atmospheric nitrate contributes notably to total aerosol mass in the present day and is likely to be more important over the next century, with a projected decline in SO2 and NOx emissions and increase in NH3 emissions. This paper investigates atmospheric nitrate using multiple global models and measurements. The study is part of the AeroCom phase III activity. The study is the first attempt to look at global atmospheric nitrate simulation at physical and chemical process levels.
Keiichiro Hara, Sumito Matoba, Motohiro Hirabayashi, and Tetsuhide Yamasaki
Atmos. Chem. Phys., 17, 8577–8598, https://doi.org/10.5194/acp-17-8577-2017, https://doi.org/10.5194/acp-17-8577-2017, 2017
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To obtain knowledge about sea-salt chemistry in polar regions, we made simultaneous measurements and sampling of aerosols, frost flowers, and brine around northwestern Greenland during winter–spring. Our results show sea-salt enrichment in frost flowers and snow. Also, the fractionated sea-salt particles were suspended in the atmosphere over sea-ice areas. From the field evidence and results from earlier studies, we propose and describe sea-salt cycles in seasonal sea-ice areas.
Tatsuya Nagashima, Kengo Sudo, Hajime Akimoto, Junichi Kurokawa, and Toshimasa Ohara
Atmos. Chem. Phys., 17, 8231–8246, https://doi.org/10.5194/acp-17-8231-2017, https://doi.org/10.5194/acp-17-8231-2017, 2017
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We showed the large contribution of different source regions in Asia to the recent increasing trend in surface ozone over Japan by using a global chemical transport model. China accounted for the largest part of the increasing trend, not only through the domestic ozone production (36 %) but also the ozone production in the adjacent countries due to the ozone precursors emitted in China (10 %). Other factors such as temporal change in climate and methane concentration were also investigated.
Min Huang, Gregory R. Carmichael, R. Bradley Pierce, Duseong S. Jo, Rokjin J. Park, Johannes Flemming, Louisa K. Emmons, Kevin W. Bowman, Daven K. Henze, Yanko Davila, Kengo Sudo, Jan Eiof Jonson, Marianne Tronstad Lund, Greet Janssens-Maenhout, Frank J. Dentener, Terry J. Keating, Hilke Oetjen, and Vivienne H. Payne
Atmos. Chem. Phys., 17, 5721–5750, https://doi.org/10.5194/acp-17-5721-2017, https://doi.org/10.5194/acp-17-5721-2017, 2017
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In support of the HTAP phase 2 experiment, we conducted a number of regional-scale Sulfur Transport and dEposition Model base and sensitivity simulations over North America during May–June 2010. The STEM chemical boundary conditions were downscaled from three (GEOS-Chem, RAQMS, and ECMWF C-IFS) global chemical transport models' simulations. Analyses were performed on large spatial–temporal scales relative to HTAP1 and also on subcontinental and event scales including the use of satellite data.
Syuichi Itahashi, Itsushi Uno, Kazuo Osada, Yusuke Kamiguchi, Shigekazu Yamamoto, Kei Tamura, Zhe Wang, Yasunori Kurosaki, and Yugo Kanaya
Atmos. Chem. Phys., 17, 3823–3843, https://doi.org/10.5194/acp-17-3823-2017, https://doi.org/10.5194/acp-17-3823-2017, 2017
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Over East Asia, the transboundary air pollution of SO42− has been recognized. The importance of the transboundary air pollution of NO3− in winter was demonstrated in this study through synergetic ground-based observations with state-of-the-art measurements of secondary inorganic aerosols (SO42−, NO3−, and NH4+) and a regional chemical transport model analysis. This study will help to refine the understanding of transboundary heavy PM2.5 pollution in winter.
Hubert Luce, Lakshmi Kantha, Hiroyuki Hashiguchi, Dale Lawrence, Masanori Yabuki, Toshitaka Tsuda, and Tyler Mixa
Ann. Geophys., 35, 423–441, https://doi.org/10.5194/angeo-35-423-2017, https://doi.org/10.5194/angeo-35-423-2017, 2017
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Results of comparisons between data collected from a VHF Doppler radar and small unmanned aerial vehicles (UAVs) are presented. The UAVs, equipped with meteorological sensors, flew nearby the radar up to an altitude of ~ 4.0 km. Both instruments detected the same clear-air refractive index gradients at a vertical scale of ~ 20 m when the vertical stratification was strong. A VHF radar can thus provide a faithful image of the vertical stratification of the atmosphere down to decimeter scales.
Olaf Morgenstern, Michaela I. Hegglin, Eugene Rozanov, Fiona M. O'Connor, N. Luke Abraham, Hideharu Akiyoshi, Alexander T. Archibald, Slimane Bekki, Neal Butchart, Martyn P. Chipperfield, Makoto Deushi, Sandip S. Dhomse, Rolando R. Garcia, Steven C. Hardiman, Larry W. Horowitz, Patrick Jöckel, Beatrice Josse, Douglas Kinnison, Meiyun Lin, Eva Mancini, Michael E. Manyin, Marion Marchand, Virginie Marécal, Martine Michou, Luke D. Oman, Giovanni Pitari, David A. Plummer, Laura E. Revell, David Saint-Martin, Robyn Schofield, Andrea Stenke, Kane Stone, Kengo Sudo, Taichu Y. Tanaka, Simone Tilmes, Yousuke Yamashita, Kohei Yoshida, and Guang Zeng
Geosci. Model Dev., 10, 639–671, https://doi.org/10.5194/gmd-10-639-2017, https://doi.org/10.5194/gmd-10-639-2017, 2017
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We present a review of the make-up of 20 models participating in the Chemistry–Climate Model Initiative (CCMI). In comparison to earlier such activities, most of these models comprise a whole-atmosphere chemistry, and several of them include an interactive ocean module. This makes them suitable for studying the interactions of tropospheric air quality, stratospheric ozone, and climate. The paper lays the foundation for other studies using the CCMI simulations for scientific analysis.
Kazuyuki Miyazaki, Henk Eskes, Kengo Sudo, K. Folkert Boersma, Kevin Bowman, and Yugo Kanaya
Atmos. Chem. Phys., 17, 807–837, https://doi.org/10.5194/acp-17-807-2017, https://doi.org/10.5194/acp-17-807-2017, 2017
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Global surface emissions of nitrogen oxides (NOx) over a 10-year period (2005–2014) are estimated from assimilation of multiple satellite datasets. We present detailed distributions of the estimated NOx emission distributions for all major regions, the diurnal, seasonal, and decadal variability. The estimated emissions show a positive trend over India, China, and the Middle East, and a negative trend over the United States, southern Africa, and western Europe.
Camilla Weum Stjern, Bjørn Hallvard Samset, Gunnar Myhre, Huisheng Bian, Mian Chin, Yanko Davila, Frank Dentener, Louisa Emmons, Johannes Flemming, Amund Søvde Haslerud, Daven Henze, Jan Eiof Jonson, Tom Kucsera, Marianne Tronstad Lund, Michael Schulz, Kengo Sudo, Toshihiko Takemura, and Simone Tilmes
Atmos. Chem. Phys., 16, 13579–13599, https://doi.org/10.5194/acp-16-13579-2016, https://doi.org/10.5194/acp-16-13579-2016, 2016
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Air pollution can reach distant regions through intercontinental transport. Here we first present results from the Hemispheric Transport of Air Pollution Phase 2 exercise, where many models performed the same set of coordinated emission-reduction experiments. We find that mitigations have considerable extra-regional effects, and show that this is particularly true for black carbon emissions, as long-range transport elevates aerosols to higher levels where their radiative influence is stronger.
Xiaole Pan, Itsushi Uno, Yukari Hara, Kazuo Osada, Shigekazu Yamamoto, Zhe Wang, Nobuo Sugimoto, Hiroshi Kobayashi, and Zifa Wang
Atmos. Chem. Phys., 16, 9863–9873, https://doi.org/10.5194/acp-16-9863-2016, https://doi.org/10.5194/acp-16-9863-2016, 2016
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Polarization properties of aerosol particles at a suburban site in the western Japan was studied on the basis of long-term observation and trajectory analysis. This study provides the detailed information on the polarization characteristics of particles from different origins, and proposed a reliable criterion to classify spherical and non-spherical particles. This study introduced a new method to investigate the mixed state of dust particle with anthropogenic pollutant.
Raquel A. Silva, J. Jason West, Jean-François Lamarque, Drew T. Shindell, William J. Collins, Stig Dalsoren, Greg Faluvegi, Gerd Folberth, Larry W. Horowitz, Tatsuya Nagashima, Vaishali Naik, Steven T. Rumbold, Kengo Sudo, Toshihiko Takemura, Daniel Bergmann, Philip Cameron-Smith, Irene Cionni, Ruth M. Doherty, Veronika Eyring, Beatrice Josse, Ian A. MacKenzie, David Plummer, Mattia Righi, David S. Stevenson, Sarah Strode, Sophie Szopa, and Guang Zengast
Atmos. Chem. Phys., 16, 9847–9862, https://doi.org/10.5194/acp-16-9847-2016, https://doi.org/10.5194/acp-16-9847-2016, 2016
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Using ozone and PM2.5 concentrations from the ACCMIP ensemble of chemistry-climate models for the four Representative Concentration Pathway scenarios (RCPs), together with projections of future population and baseline mortality rates, we quantify the human premature mortality impacts of future ambient air pollution in 2030, 2050 and 2100, relative to 2000 concentrations. We also estimate the global mortality burden of ozone and PM2.5 in 2000 and each future period.
J. L. Schnell, M. J. Prather, B. Josse, V. Naik, L. W. Horowitz, P. Cameron-Smith, D. Bergmann, G. Zeng, D. A. Plummer, K. Sudo, T. Nagashima, D. T. Shindell, G. Faluvegi, and S. A. Strode
Atmos. Chem. Phys., 15, 10581–10596, https://doi.org/10.5194/acp-15-10581-2015, https://doi.org/10.5194/acp-15-10581-2015, 2015
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We test global chemistry--climate models in their ability to simulate present-day surface ozone. Models are tested against observed hourly ozone from 4217 stations in North America and Europe that are averaged over 1°x1° grid cells. Using novel metrics, we find most models match the shape but not the amplitude of regional summertime diurnal and annual cycles and match the pattern but not the magnitude of summer ozone enhancement. Most also match the observed distribution of extreme episode sizes
K. Miyazaki, H. J. Eskes, and K. Sudo
Atmos. Chem. Phys., 15, 8315–8348, https://doi.org/10.5194/acp-15-8315-2015, https://doi.org/10.5194/acp-15-8315-2015, 2015
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This paper reports on an 8-year reanalysis of tropospheric chemistry based on an assimilation of multiple satellite-derived data sets. The reanalysis performed well on regional and global scales and for seasonal and interannual variations. The simultaneous assimilation of multiple-species data, involving the optimisation of both concentration and emission fields, provides unique information on year-to-year variations in the atmospheric environment.
K. Ishijima, M. Takigawa, K. Sudo, S. Toyoda, N. Yoshida, T. Röckmann, J. Kaiser, S. Aoki, S. Morimoto, S. Sugawara, and T. Nakazawa
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acpd-15-19947-2015, https://doi.org/10.5194/acpd-15-19947-2015, 2015
Revised manuscript not accepted
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We developed an atmospheric N2O isotopocule model based on a chemistry-coupled atmospheric general circulation model and a simple method to optimize the model, and estimated the isotopic signatures of surface sources at the hemispheric scale. Data obtained from ground-based observations, measurements of firn air, and balloon and aircraft flights were used to optimize the long-term trends, interhemispheric gradients, and photolytic fractionation, respectively, in the model.
K. Hara, F. Nakazawa, S. Fujita, K. Fukui, H. Enomoto, and S. Sugiyama
Atmos. Chem. Phys., 14, 10211–10230, https://doi.org/10.5194/acp-14-10211-2014, https://doi.org/10.5194/acp-14-10211-2014, 2014
Y. Kanaya, H. Irie, H. Takashima, H. Iwabuchi, H. Akimoto, K. Sudo, M. Gu, J. Chong, Y. J. Kim, H. Lee, A. Li, F. Si, J. Xu, P.-H. Xie, W.-Q. Liu, A. Dzhola, O. Postylyakov, V. Ivanov, E. Grechko, S. Terpugova, and M. Panchenko
Atmos. Chem. Phys., 14, 7909–7927, https://doi.org/10.5194/acp-14-7909-2014, https://doi.org/10.5194/acp-14-7909-2014, 2014
K. Hara, M. Hayashi, M. Yabuki, M. Shiobara, and C. Nishita-Hara
Atmos. Chem. Phys., 14, 4169–4183, https://doi.org/10.5194/acp-14-4169-2014, https://doi.org/10.5194/acp-14-4169-2014, 2014
K. Miyazaki, H. J. Eskes, K. Sudo, and C. Zhang
Atmos. Chem. Phys., 14, 3277–3305, https://doi.org/10.5194/acp-14-3277-2014, https://doi.org/10.5194/acp-14-3277-2014, 2014
K. Osada, S. Ura, M. Kagawa, M. Mikami, T. Y. Tanaka, S. Matoba, K. Aoki, M. Shinoda, Y. Kurosaki, M. Hayashi, A. Shimizu, and M. Uematsu
Atmos. Chem. Phys., 14, 1107–1121, https://doi.org/10.5194/acp-14-1107-2014, https://doi.org/10.5194/acp-14-1107-2014, 2014
K. Hara, K. Osada, and T. Yamanouchi
Atmos. Chem. Phys., 13, 9119–9139, https://doi.org/10.5194/acp-13-9119-2013, https://doi.org/10.5194/acp-13-9119-2013, 2013
V. Naik, A. Voulgarakis, A. M. Fiore, L. W. Horowitz, J.-F. Lamarque, M. Lin, M. J. Prather, P. J. Young, D. Bergmann, P. J. Cameron-Smith, I. Cionni, W. J. Collins, S. B. Dalsøren, R. Doherty, V. Eyring, G. Faluvegi, G. A. Folberth, B. Josse, Y. H. Lee, I. A. MacKenzie, T. Nagashima, T. P. C. van Noije, D. A. Plummer, M. Righi, S. T. Rumbold, R. Skeie, D. T. Shindell, D. S. Stevenson, S. Strode, K. Sudo, S. Szopa, and G. Zeng
Atmos. Chem. Phys., 13, 5277–5298, https://doi.org/10.5194/acp-13-5277-2013, https://doi.org/10.5194/acp-13-5277-2013, 2013
K. W. Bowman, D. T. Shindell, H. M. Worden, J.F. Lamarque, P. J. Young, D. S. Stevenson, Z. Qu, M. de la Torre, D. Bergmann, P. J. Cameron-Smith, W. J. Collins, R. Doherty, S. B. Dalsøren, G. Faluvegi, G. Folberth, L. W. Horowitz, B. M. Josse, Y. H. Lee, I. A. MacKenzie, G. Myhre, T. Nagashima, V. Naik, D. A. Plummer, S. T. Rumbold, R. B. Skeie, S. A. Strode, K. Sudo, S. Szopa, A. Voulgarakis, G. Zeng, S. S. Kulawik, A. M. Aghedo, and J. R. Worden
Atmos. Chem. Phys., 13, 4057–4072, https://doi.org/10.5194/acp-13-4057-2013, https://doi.org/10.5194/acp-13-4057-2013, 2013
D. T. Shindell, J.-F. Lamarque, M. Schulz, M. Flanner, C. Jiao, M. Chin, P. J. Young, Y. H. Lee, L. Rotstayn, N. Mahowald, G. Milly, G. Faluvegi, Y. Balkanski, W. J. Collins, A. J. Conley, S. Dalsoren, R. Easter, S. Ghan, L. Horowitz, X. Liu, G. Myhre, T. Nagashima, V. Naik, S. T. Rumbold, R. Skeie, K. Sudo, S. Szopa, T. Takemura, A. Voulgarakis, J.-H. Yoon, and F. Lo
Atmos. Chem. Phys., 13, 2939–2974, https://doi.org/10.5194/acp-13-2939-2013, https://doi.org/10.5194/acp-13-2939-2013, 2013
D. S. Stevenson, P. J. Young, V. Naik, J.-F. Lamarque, D. T. Shindell, A. Voulgarakis, R. B. Skeie, S. B. Dalsoren, G. Myhre, T. K. Berntsen, G. A. Folberth, S. T. Rumbold, W. J. Collins, I. A. MacKenzie, R. M. Doherty, G. Zeng, T. P. C. van Noije, A. Strunk, D. Bergmann, P. Cameron-Smith, D. A. Plummer, S. A. Strode, L. Horowitz, Y. H. Lee, S. Szopa, K. Sudo, T. Nagashima, B. Josse, I. Cionni, M. Righi, V. Eyring, A. Conley, K. W. Bowman, O. Wild, and A. Archibald
Atmos. Chem. Phys., 13, 3063–3085, https://doi.org/10.5194/acp-13-3063-2013, https://doi.org/10.5194/acp-13-3063-2013, 2013
Y. H. Lee, J.-F. Lamarque, M. G. Flanner, C. Jiao, D. T. Shindell, T. Berntsen, M. M. Bisiaux, J. Cao, W. J. Collins, M. Curran, R. Edwards, G. Faluvegi, S. Ghan, L. W. Horowitz, J. R. McConnell, J. Ming, G. Myhre, T. Nagashima, V. Naik, S. T. Rumbold, R. B. Skeie, K. Sudo, T. Takemura, F. Thevenon, B. Xu, and J.-H. Yoon
Atmos. Chem. Phys., 13, 2607–2634, https://doi.org/10.5194/acp-13-2607-2013, https://doi.org/10.5194/acp-13-2607-2013, 2013
A. Voulgarakis, V. Naik, J.-F. Lamarque, D. T. Shindell, P. J. Young, M. J. Prather, O. Wild, R. D. Field, D. Bergmann, P. Cameron-Smith, I. Cionni, W. J. Collins, S. B. Dalsøren, R. M. Doherty, V. Eyring, G. Faluvegi, G. A. Folberth, L. W. Horowitz, B. Josse, I. A. MacKenzie, T. Nagashima, D. A. Plummer, M. Righi, S. T. Rumbold, D. S. Stevenson, S. A. Strode, K. Sudo, S. Szopa, and G. Zeng
Atmos. Chem. Phys., 13, 2563–2587, https://doi.org/10.5194/acp-13-2563-2013, https://doi.org/10.5194/acp-13-2563-2013, 2013
P. J. Young, A. T. Archibald, K. W. Bowman, J.-F. Lamarque, V. Naik, D. S. Stevenson, S. Tilmes, A. Voulgarakis, O. Wild, D. Bergmann, P. Cameron-Smith, I. Cionni, W. J. Collins, S. B. Dalsøren, R. M. Doherty, V. Eyring, G. Faluvegi, L. W. Horowitz, B. Josse, Y. H. Lee, I. A. MacKenzie, T. Nagashima, D. A. Plummer, M. Righi, S. T. Rumbold, R. B. Skeie, D. T. Shindell, S. A. Strode, K. Sudo, S. Szopa, and G. Zeng
Atmos. Chem. Phys., 13, 2063–2090, https://doi.org/10.5194/acp-13-2063-2013, https://doi.org/10.5194/acp-13-2063-2013, 2013
J.-F. Lamarque, D. T. Shindell, B. Josse, P. J. Young, I. Cionni, V. Eyring, D. Bergmann, P. Cameron-Smith, W. J. Collins, R. Doherty, S. Dalsoren, G. Faluvegi, G. Folberth, S. J. Ghan, L. W. Horowitz, Y. H. Lee, I. A. MacKenzie, T. Nagashima, V. Naik, D. Plummer, M. Righi, S. T. Rumbold, M. Schulz, R. B. Skeie, D. S. Stevenson, S. Strode, K. Sudo, S. Szopa, A. Voulgarakis, and G. Zeng
Geosci. Model Dev., 6, 179–206, https://doi.org/10.5194/gmd-6-179-2013, https://doi.org/10.5194/gmd-6-179-2013, 2013
Related subject area
Subject: Aerosols | Research Activity: Field Measurements | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Measurement report: Sources and meteorology influencing highly time-resolved PM2.5 trace elements at three urban sites in the extremely polluted Indo-Gangetic Plain in India
Formation of highly absorptive secondary brown carbon through nighttime multiphase chemistry of biomass burning emissions
Measurement report: Vertically resolved atmospheric properties observed over the Southern Great Plains with the ArcticShark uncrewed aerial system
Non-biogenic sources are an important but overlooked contributor to aerosol isoprene-derived organosulfates during winter in northern China
The critical role of aqueous-phase processes in aromatic-derived nitrogen-containing organic aerosol formation in cities with different energy consumption patterns
Characterization of atmospheric water-soluble brown carbon in the Athabasca oil sands region, Canada
Sensitivity of aerosol and cloud properties to coupling strength of marine boundary layer clouds over the northwest Atlantic
Burning conditions and transportation pathways determine biomass-burning aerosol properties in the Ascension Island marine boundary layer
Observations of high-time-resolution and size-resolved aerosol chemical composition and microphysics in the central Arctic: implications for climate-relevant particle properties
Measurement report: Brown carbon aerosol in rural Germany – sources, chemistry, and diurnal variations
Multiple eco-regions contribute to the seasonal cycle of Antarctic aerosol size distributions
Seasonal investigation of ultrafine-particle organic composition in an eastern Amazonian rainforest
High-resolution analyses of concentrations and sizes of refractory black carbon particles deposited in northwestern Greenland over the past 350 years – Part 2: Seasonal and temporal trends in refractory black carbon originated from fossil fuel combustion and biomass burning
Direct measurement of N2O5 heterogeneous uptake coefficients on atmospheric aerosols in southwestern China and evaluation of current parameterizations
Measurement report: Per- and polyfluoroalkyl substances (PFAS) in particulate matter (PM10) from activated sludge aeration
Significant role of biomass burning in heavy haze formation in Nanjing, a megacity in China: molecular-level insights from intensive PM2.5 sampling on winter hazy days
Widespread trace bromine and iodine in remote tropospheric non-sea-salt aerosols
A 60-year atmospheric nitrate isotope record from a Southeast Greenland ice core with minimal post-depositional alteration
Formation and chemical evolution of secondary organic aerosol in two different environments: a dual-chamber study
Technical note: Quantified organic aerosol subsaturated hygroscopicity by a simple optical scatter monitor system through field measurements
Measurement report: Oxidation potential of water-soluble aerosol components in the south and north of Beijing
Enhanced daytime secondary aerosol formation driven by gas–particle partitioning in downwind urban plumes
Understanding the mechanism and importance of brown carbon bleaching across the visible spectrum in biomass burning plumes from the WE-CAN campaign
Influence of terrestrial and marine air mass on the constituents and intermixing of bioaerosols over a coastal atmosphere
A multi-site passive approach to studying the emissions and evolution of smoke from prescribed fires
The annual cycle and sources of relevant aerosol precursor vapors in the central Arctic during the MOSAiC expedition
Enhanced emission of intermediate/semi-volatile organic matters in both gas and particle phases from ship exhausts with low-sulfur fuels
African dust transported to Barbados in the Wintertime Lacks Indicators of Chemical Aging
Opinion: How will advances in aerosol science inform our understanding of the health impacts of outdoor particulate pollution?
Measurement report: Intra-annual variability of black carbon and brown carbon and their interrelation with meteorological conditions over Gangtok, Sikkim
Long-range transport of air pollutants increases the concentration of hazardous components of PM2.5 in northern South America
Molecular characterization of organic aerosols in urban and forested areas of Paris using high resolution mass spectrometry
Dominant influence of biomass combustion and cross-border transport on nitrogen-containing organic compound levels in the southeastern Tibetan Plateau
Measurement report: Wintertime aerosol characterization at an urban traffic site in Helsinki Finland
Impacts of elevated anthropogenic emissions on physicochemical characteristics of black-carbon-containing particles over the Tibetan Plateau
Online characterization of primary and secondary emissions of particulate matter and acidic molecules from a modern fleet of city buses
Atmospheric evolution of environmentally persistent free radicals in the rural North China Plain: effects on water solubility and PM2.5 oxidative potential
Measurement report: Characterization of Aerosol Hygroscopicity over Southeast Asia during the NASA CAMP2Ex Campaign
Two distinct ship emission profiles for organic-sulfate source apportionment of PM in sulfur emission control areas
Measurement report: In-depth characterization of ship emissions during operations in a Mediterranean port
Automated compound speciation, cluster analysis, and quantification of organic vapors and aerosols using comprehensive two-dimensional gas chromatography and mass spectrometry
Marine Organic Aerosols at Mace Head: Effects from Phytoplankton and Source Region Variability
Measurement report: Occurrence of aminiums in PM2.5 during winter in China – aminium outbreak during polluted episodes and potential constraints
Bridging gas and aerosol properties between the northeastern US and Bermuda: analysis of eight transit flights
The behaviour of charged particles (ions) during new particle formation events in urban Leipzig, Germany
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
Ashutosh K. Shukla, Sachchida N. Tripathi, Shamitaksha Talukdar, Vishnu Murari, Sreenivas Gaddamidi, Manousos-Ioannis Manousakas, Vipul Lalchandani, Kuldeep Dixit, Vinayak M. Ruge, Peeyush Khare, Mayank Kumar, Vikram Singh, Neeraj Rastogi, Suresh Tiwari, Atul K. Srivastava, Dilip Ganguly, Kaspar Rudolf Daellenbach, and André S. H. Prévôt
Atmos. Chem. Phys., 25, 3765–3784, https://doi.org/10.5194/acp-25-3765-2025, https://doi.org/10.5194/acp-25-3765-2025, 2025
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Our study delves into the elemental composition of aerosols at three sites across the Indo-Gangetic Plain (IGP), revealing distinct patterns during pollution episodes. We found significant increases in chlorine (Cl)-rich and solid fuel combustion (SFC) sources, indicating dynamic emission sources, agricultural burning impacts, and meteorological influences. Surges in Cl-rich particles during cold periods highlight their role in particle growth under high-relative-humidity conditions.
Ye Kuang, Biao Luo, Shan Huang, Junwen Liu, Weiwei Hu, Yuwen Peng, Duohong Chen, Dingli Yue, Wanyun Xu, Bin Yuan, and Min Shao
Atmos. Chem. Phys., 25, 3737–3752, https://doi.org/10.5194/acp-25-3737-2025, https://doi.org/10.5194/acp-25-3737-2025, 2025
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This research reveals the potential importance of nighttime NO3 radical chemistry and aerosol water in the rapid formation of secondary brown carbon from diluted biomass burning emissions. The findings enhance our understanding of nighttime biomass burning evolution and its implications for climate and regional air quality, especially regarding interactions with background aerosol water and water-rich fogs and clouds.
Fan Mei, Qi Zhang, Damao Zhang, Jerome D. Fast, Gourihar Kulkarni, Mikhail S. Pekour, Christopher R. Niedek, Susanne Glienke, Israel Silber, Beat Schmid, Jason M. Tomlinson, Hardeep S. Mehta, Xena Mansoura, Zezhen Cheng, Gregory W. Vandergrift, Nurun Nahar Lata, Swarup China, and Zihua Zhu
Atmos. Chem. Phys., 25, 3425–3444, https://doi.org/10.5194/acp-25-3425-2025, https://doi.org/10.5194/acp-25-3425-2025, 2025
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This study highlights the unique capability of the ArcticShark, an uncrewed aerial system, in measuring vertically resolved atmospheric properties. Data from 32 research flights in 2023 reveal seasonal patterns and correlations with conventional measurements. The consistency and complementarity of in situ and remote sensing methods are highlighted. The study demonstrates the ArcticShark’s versatility in bridging data gaps and improving the understanding of vertical atmospheric structures.
Ting Yang, Yu Xu, Yu-Chen Wang, Yi-Jia Ma, Hong-Wei Xiao, Hao Xiao, and Hua-Yun Xiao
Atmos. Chem. Phys., 25, 2967–2978, https://doi.org/10.5194/acp-25-2967-2025, https://doi.org/10.5194/acp-25-2967-2025, 2025
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Previous measurement–model comparisons of atmospheric isoprene levels showed a significant unidentified source of isoprene in some northern Chinese cities during winter. Here, the first combination of large-scale observations and field combustion experiments provides novel insights into biomass burning emissions as a significant source of isoprene-derived organosulfates during winter in northern cities of China.
Yi-Jia Ma, Yu Xu, Ting Yang, Lin Gui, Hong-Wei Xiao, Hao Xiao, and Hua-Yun Xiao
Atmos. Chem. Phys., 25, 2763–2780, https://doi.org/10.5194/acp-25-2763-2025, https://doi.org/10.5194/acp-25-2763-2025, 2025
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The abundance, potential precursors, and main formation mechanisms of nitrogen-containing organic compounds (NOCs) in PM2.5 during winter were compared among cities with different energy consumption patterns. The aerosol NOC pollution during winter in China is closely associated with the intensity of precursor emissions and the aqueous-phase processes. Our results highlight the importance of emission reduction strategies in controlling aerosol NOCs pollution during winter in China.
Dane Blanchard, Mark Gordon, Duc Huy Dang, Paul Andrew Makar, and Julian Aherne
Atmos. Chem. Phys., 25, 2423–2442, https://doi.org/10.5194/acp-25-2423-2025, https://doi.org/10.5194/acp-25-2423-2025, 2025
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This study offers the first known evaluation of water-soluble brown carbon aerosols in the Athabasca oil sands region (AOSR), Canada. Fluorescence spectroscopy analysis of aerosol samples from five regional sites (collected during the summer of 2021) identified oil sands operations as a measurable brown carbon source. Industrial aerosol emissions were unlikely to impact regional radiative forcing. These findings show that fluorescence spectroscopy can be used to monitor brown carbon in the AOSR.
Kira Zeider, Kayla McCauley, Sanja Dmitrovic, Leong Wai Siu, Yonghoon Choi, Ewan C. Crosbie, Joshua P. DiGangi, Glenn S. Diskin, Simon Kirschler, John B. Nowak, Michael A. Shook, Kenneth L. Thornhill, Christiane Voigt, Edward L. Winstead, Luke D. Ziemba, Paquita Zuidema, and Armin Sorooshian
Atmos. Chem. Phys., 25, 2407–2422, https://doi.org/10.5194/acp-25-2407-2025, https://doi.org/10.5194/acp-25-2407-2025, 2025
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In situ aircraft data collected over the northwest Atlantic Ocean are utilized to compare aerosol conditions and turbulence between near-surface and below-cloud-base altitudes for different regimes of coupling strength between those two levels, along with how cloud microphysical properties vary across those regimes. Stronger coupling yields more homogenous aerosol structure vertically along with higher cloud drop concentrations and sea salt influence in clouds.
Amie Dobracki, Ernie R. Lewis, Arthur J. Sedlacek III, Tyler Tatro, Maria A. Zawadowicz, and Paquita Zuidema
Atmos. Chem. Phys., 25, 2333–2363, https://doi.org/10.5194/acp-25-2333-2025, https://doi.org/10.5194/acp-25-2333-2025, 2025
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Biomass-burning aerosol is commonly present in the marine boundary layer over the southeast Atlantic Ocean between June and October. Our research indicates that burning conditions, aerosol transport pathways, and prolonged oxidation processes (heterogeneous and aqueous phases) determine the chemical, microphysical, and optical properties of the boundary layer aerosol. Notably, we find that the aerosol optical properties can be estimated from the chemical properties alone.
Benjamin Heutte, Nora Bergner, Hélène Angot, Jakob B. Pernov, Lubna Dada, Jessica A. Mirrielees, Ivo Beck, Andrea Baccarini, Matthew Boyer, Jessie M. Creamean, Kaspar R. Daellenbach, Imad El Haddad, Markus M. Frey, Silvia Henning, Tiia Laurila, Vaios Moschos, Tuukka Petäjä, Kerri A. Pratt, Lauriane L. J. Quéléver, Matthew D. Shupe, Paul Zieger, Tuija Jokinen, and Julia Schmale
Atmos. Chem. Phys., 25, 2207–2241, https://doi.org/10.5194/acp-25-2207-2025, https://doi.org/10.5194/acp-25-2207-2025, 2025
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Limited aerosol measurements in the central Arctic hinder our understanding of aerosol–climate interactions in the region. Our year-long observations of aerosol physicochemical properties during the MOSAiC expedition reveal strong seasonal variations in aerosol chemical composition, where the short-term variability is heavily affected by storms in the Arctic. Local wind-generated particles are shown to be an important source of cloud seeds, especially in autumn.
Feng Jiang, Harald Saathoff, Uzoamaka Ezenobi, Junwei Song, Hengheng Zhang, Linyu Gao, and Thomas Leisner
Atmos. Chem. Phys., 25, 1917–1930, https://doi.org/10.5194/acp-25-1917-2025, https://doi.org/10.5194/acp-25-1917-2025, 2025
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The chemical composition of brown carbon in the particle and gas phase was determined by mass spectrometry. BrC in the gas phase was mainly controlled by secondary formation and particle-to-gas partitioning. BrC in the particle phase was mainly from secondary formation. This work helps to get a better understanding of diurnal variations and the sources of brown carbon aerosol at a rural location in central Europe.
James Brean, David C. S. Beddows, Eija Asmi, Aki Virkkula, Lauriane L. J. Quéléver, Mikko Sipilä, Floortje Van Den Heuvel, Thomas Lachlan-Cope, Anna Jones, Markus Frey, Angelo Lupi, Jiyeon Park, Young Jun Yoon, Rolf Weller, Giselle L. Marincovich, Gabriela C. Mulena, Roy M. Harrison, and Manuel Dall'Osto
Atmos. Chem. Phys., 25, 1145–1162, https://doi.org/10.5194/acp-25-1145-2025, https://doi.org/10.5194/acp-25-1145-2025, 2025
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Our results emphasise how understanding the geographical variation in surface types across the Antarctic is key to understanding secondary aerosol sources.
Adam E. Thomas, Hayley S. Glicker, Alex B. Guenther, Roger Seco, Oscar Vega Bustillos, Julio Tota, Rodrigo A. F. Souza, and James N. Smith
Atmos. Chem. Phys., 25, 959–977, https://doi.org/10.5194/acp-25-959-2025, https://doi.org/10.5194/acp-25-959-2025, 2025
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We present measurements of the organic composition of ultrafine particles collected from the eastern Amazon, an understudied region that is subjected to increasing human influence. We find that while isoprene chemistry is likely significant for ultrafine-particle growth throughout the year, compounds related to other sources, such as biological-spore emissions and biomass burning, exhibit striking seasonal differences, implying extensive variation in regional ultrafine-particle sources.
Kumiko Goto-Azuma, Yoshimi Ogawa-Tsukagawa, Kaori Fukuda, Koji Fujita, Motohiro Hirabayashi, Remi Dallmayr, Jun Ogata, Nobuhiro Moteki, Tatsuhiro Mori, Sho Ohata, Yutaka Kondo, Makoto Koike, Sumito Matoba, Moe Kadota, Akane Tsushima, Naoko Nagatsuka, and Teruo Aoki
Atmos. Chem. Phys., 25, 657–683, https://doi.org/10.5194/acp-25-657-2025, https://doi.org/10.5194/acp-25-657-2025, 2025
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Monthly ice core records spanning 350 years from Greenland show trends in refractory black carbon (rBC) concentrations and sizes. rBC levels have increased since the 1870s due to the inflow of anthropogenic rBC, with larger diameters than those from biomass burning (BB) rBC. High summer BB rBC peaks may reduce the ice sheet albedo, but BB rBC showed no increase until the early 2000s. These results are vital for validating aerosol and climate models.
Jiayin Li, Tianyu Zhai, Xiaorui Chen, Haichao Wang, Shuyang Xie, Shiyi Chen, Chunmeng Li, Huabin Dong, and Keding Lu
EGUsphere, https://doi.org/10.5194/egusphere-2024-3804, https://doi.org/10.5194/egusphere-2024-3804, 2025
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We directly measured the dinitrogen pentoxide (N2O5) uptake coefficient which critical impact the NOx fate and particulate nitrate formation in a typical highland city, Kunming, in China. We found the performance of current γ(N2O5) parameterizations showed deviations with the varying aerosol liquid water content (ALWC). Such differences would lead to biased estimation on particulate nitrate production potential. Our findings suggest the directions for future studies.
Jishnu Pandamkulangara Kizhakkethil, Zongbo Shi, Anna Bogush, and Ivan Kourtchev
EGUsphere, https://doi.org/10.5194/egusphere-2024-3952, https://doi.org/10.5194/egusphere-2024-3952, 2025
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Pollution with per- and polyfluoroalkyl substances (PFAS) received attention due to their environmental persistence and bioaccumulation. PM10 collected above a scaled-down activated sludge tank treating domestic sewage for a population >10,000 people in the UK were analysed for a range of short-, medium- and long-chain PFAS. Eight PFAS were detected in the PM10. Our results suggest that wastewater treatment processes i.e. activated sludge aeration could aerosolise PFAS into airborne PM.
Mingjie Kang, Mengying Bao, Wenhuai Song, Aduburexiati Abulimiti, Changliu Wu, Fang Cao, Sönke Szidat, and Yanlin Zhang
Atmos. Chem. Phys., 25, 73–91, https://doi.org/10.5194/acp-25-73-2025, https://doi.org/10.5194/acp-25-73-2025, 2025
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Reports on molecular-level knowledge of high-temporal-resolution particulate matter ≤2.5 µm in diameter (PM2.5) on hazy days are limited. We investigated various PM2.5 species and their sources. The results show biomass burning (BB) was the main source of organic carbon. Moreover, BB enhanced fungal spore emissions and secondary aerosol formation. The contribution of non-fossil sources increased with increasing haze pollution, suggesting BB may be an important driver of haze events in winter.
Gregory P. Schill, Karl D. Froyd, Daniel M. Murphy, Christina J. Williamson, Charles A. Brock, Tomás Sherwen, Mat J. Evans, Eric A. Ray, Eric C. Apel, Rebecca S. Hornbrook, Alan J. Hills, Jeff Peischl, Thomas B. Ryerson, Chelsea R. Thompson, Ilann Bourgeois, Donald R. Blake, Joshua P. DiGangi, and Glenn S. Diskin
Atmos. Chem. Phys., 25, 45–71, https://doi.org/10.5194/acp-25-45-2025, https://doi.org/10.5194/acp-25-45-2025, 2025
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Using single-particle mass spectrometry, we show that trace concentrations of bromine and iodine are ubiquitous in remote tropospheric aerosol and suggest that aerosols are an important part of the global reactive iodine budget. Comparisons to a global climate model with detailed iodine chemistry are favorable in the background atmosphere; however, the model cannot replicate our measurements near the ocean surface, in biomass burning plumes, and in the stratosphere.
Zhao Wei, Shohei Hattori, Asuka Tsuruta, Zhuang Jiang, Sakiko Ishino, Koji Fujita, Sumito Matoba, Lei Geng, Alexis Lamothe, Ryu Uemura, Naohiro Yoshida, Joel Savarino, and Yoshinori Iizuka
EGUsphere, https://doi.org/10.5194/egusphere-2024-3937, https://doi.org/10.5194/egusphere-2024-3937, 2024
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Nitrate isotope records in ice cores reveal changes in NOₓ emissions, atmospheric acidity, and oxidation chemistry driven by human activity. However, nitrate in snow can be altered by UV-driven post-depositional processes, making snow accumulation rates critical for preserving these records. This study examines nitrate isotopes in an SE-Dome ice core, where high snow accumulation minimizes these effects, providing a reliable archive of atmospheric nitrogen cycling.
Andreas Aktypis, Dontavious J. Sippial, Christina N. Vasilakopoulou, Angeliki Matrali, Christos Kaltsonoudis, Andrea Simonati, Marco Paglione, Matteo Rinaldi, Stefano Decesari, and Spyros N. Pandis
Atmos. Chem. Phys., 24, 13769–13791, https://doi.org/10.5194/acp-24-13769-2024, https://doi.org/10.5194/acp-24-13769-2024, 2024
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A dual-chamber system was deployed in two different environments (Po Valley, Italy, and Pertouli forest, Greece) to study the potential of ambient air directly injected into the chambers, to form secondary organic aerosol (SOA). In the Po Valley, the system reacts rapidly, forming large amounts of SOA, while in Pertouli the SOA formation chemistry appears to have been practically terminated before the beginning of most experiments, so there is little additional SOA formation potential left.
Jie Zhang, Tianyu Zhu, Alexandra Catena, Yaowei Li, Margaret J. Schwab, Pengfei Liu, Akua Asa-Awuku, and James Schwab
Atmos. Chem. Phys., 24, 13445–13456, https://doi.org/10.5194/acp-24-13445-2024, https://doi.org/10.5194/acp-24-13445-2024, 2024
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This study shows the derived organic aerosol hygroscopicity under high-humidity conditions based on a simple optical scatter monitor system, including two nephelometric monitors (pDR-1500), when the aerosol chemical composition is already known.
Wei Yuan, Ru-Jin Huang, Chao Luo, Lu Yang, Wenjuan Cao, Jie Guo, and Huinan Yang
Atmos. Chem. Phys., 24, 13219–13230, https://doi.org/10.5194/acp-24-13219-2024, https://doi.org/10.5194/acp-24-13219-2024, 2024
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We characterized water-soluble oxidative potential (OP) levels in wintertime PM2.5 in the south and north of Beijing. Our results show that the volume-normalized dithiothreitol (DTTv) in the north was comparable to that in the south, while the mass-normalized dithiothreitol (DTTm) in the north was almost twice that in the south. Traffic-related emissions and biomass burning were the main sources of DTTv in the south, and traffic-related emissions contributed the most to DTTv in the north.
Mingfu Cai, Chenshuo Ye, Bin Yuan, Shan Huang, E Zheng, Suxia Yang, Zelong Wang, Yi Lin, Tiange Li, Weiwei Hu, Wei Chen, Qicong Song, Wei Li, Yuwen Peng, Baoling Liang, Qibin Sun, Jun Zhao, Duohong Chen, Jiaren Sun, Zhiyong Yang, and Min Shao
Atmos. Chem. Phys., 24, 13065–13079, https://doi.org/10.5194/acp-24-13065-2024, https://doi.org/10.5194/acp-24-13065-2024, 2024
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This study investigated the daytime secondary organic aerosol (SOA) formation in urban plumes. We observed a significant daytime SOA formation through gas–particle partitioning when the site was affected by urban plumes. A box model simulation indicated that urban pollutants (nitrogen oxide and volatile organic compounds) could enhance the oxidizing capacity, while the elevated volatile organic compounds were mainly responsible for promoting daytime SOA formation.
Yingjie Shen, Rudra P. Pokhrel, Amy P. Sullivan, Ezra J. T. Levin, Lauren A. Garofalo, Delphine K. Farmer, Wade Permar, Lu Hu, Darin W. Toohey, Teresa Campos, Emily V. Fischer, and Shane M. Murphy
Atmos. Chem. Phys., 24, 12881–12901, https://doi.org/10.5194/acp-24-12881-2024, https://doi.org/10.5194/acp-24-12881-2024, 2024
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The magnitude and evolution of brown carbon (BrC) absorption remain unclear, with uncertainty in climate models. Data from the WE-CAN airborne experiment show that model parameterizations overestimate the mass absorption cross section (MAC) of BrC. Observed decreases in BrC absorption with chemical markers are due to decreasing organic aerosol (OA) mass rather than a decreasing BrC MAC, which is currently implemented in models. Water-soluble BrC contributes 23 % of total absorption at 660 nm.
Qun He, Zhaowen Wang, Houfeng Liu, Pengju Xu, Rongbao Duan, Caihong Xu, Jianmin Chen, and Min Wei
Atmos. Chem. Phys., 24, 12775–12792, https://doi.org/10.5194/acp-24-12775-2024, https://doi.org/10.5194/acp-24-12775-2024, 2024
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Coastal environments provide an ideal setting for investigating the intermixing of terrestrial and marine aerosols. Terrestrial air mass constituted a larger number of microbes from anthropogenic and soil emissions, whereas saprophytic and gut microbes were predominant in marine samples. Mixed air masses indicated a fusion of marine and terrestrial aerosols, characterized by alterations in the ratio of pathogenic and saprophytic microbes when compared to either terrestrial or marine samples.
Rime El Asmar, Zongrun Li, David J. Tanner, Yongtao Hu, Susan O'Neill, L. Gregory Huey, M. Talat Odman, and Rodney J. Weber
Atmos. Chem. Phys., 24, 12749–12773, https://doi.org/10.5194/acp-24-12749-2024, https://doi.org/10.5194/acp-24-12749-2024, 2024
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Prescribed burning is an important method for managing ecosystems and preventing wildfires. However, smoke from prescribed fires can have a significant impact on air quality. Here, using a network of fixed sites and sampling throughout an extended prescribed burning period in 2 different years, we characterize emissions and evolutions of up to 8 h of PM2.5 mass, black carbon (BC), and brown carbon (BrC) in smoke from burning of forested lands in the southeastern USA.
Matthew Boyer, Diego Aliaga, Lauriane L. J. Quéléver, Silvia Bucci, Hélène Angot, Lubna Dada, Benjamin Heutte, Lisa Beck, Marina Duetsch, Andreas Stohl, Ivo Beck, Tiia Laurila, Nina Sarnela, Roseline C. Thakur, Branka Miljevic, Markku Kulmala, Tuukka Petäjä, Mikko Sipilä, Julia Schmale, and Tuija Jokinen
Atmos. Chem. Phys., 24, 12595–12621, https://doi.org/10.5194/acp-24-12595-2024, https://doi.org/10.5194/acp-24-12595-2024, 2024
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We analyze the seasonal cycle and sources of gases that are relevant for the formation of aerosol particles in the central Arctic. Since theses gases can form new particles, they can influence Arctic climate. We show that the sources of these gases are associated with changes in the Arctic environment during the year, especially with respect to sea ice. Therefore, the concentration of these gases will likely change in the future as the Arctic continues to warm.
Binyu Xiao, Fan Zhang, Zeyu Liu, Yan Zhang, Rui Li, Can Wu, Xinyi Wan, Yi Wang, Yubao Chen, Yong Han, Min Cui, Libo Zhang, Yingjun Chen, and Gehui Wang
EGUsphere, https://doi.org/10.5194/egusphere-2024-3433, https://doi.org/10.5194/egusphere-2024-3433, 2024
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Intermediate/semi-volatile organic compounds in both gas and particle phases from ship exhausts are enhanced due to the switch of fuels from low-sulfur to ultra-low-sulfur. The findings indicate that optimization is necessary for the forthcoming global implementation of an ultra-low-sulfur oil policy. Besides, we find that organic diagnostic markers of hopanes, in conjunction with the ratio of octadecanoic to tetradecanoic could be considered as potential tracers for HFO exhausts.
Haley M. Royer, Michael T. Sheridan, Hope E. Elliott, Nurun Nahar Lata, Zezhen Cheng, Swarup China, Zihua Zhu, Andrew P. Ault, and Cassandra J. Gaston
EGUsphere, https://doi.org/10.5194/egusphere-2024-3288, https://doi.org/10.5194/egusphere-2024-3288, 2024
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Saharan dust transported across the Atlantic to the Caribbean, South America, and North America is hypothesized to undergo chemical processing by inorganic and organic acids that enhances cloud droplet formation, nutrient availability, and reflectivity of. In this study, chemical analysis performed on African dust deposited over Barbados shows that acid tracers are found mostly on sea salt and smoke particles, rather than dust, indicating that dust particles undergo minimal chemical processing.
Imad El Haddad, Danielle Vienneau, Kaspar R. Daellenbach, Robin Modini, Jay G. Slowik, Abhishek Upadhyay, Petros N. Vasilakos, David Bell, Kees de Hoogh, and Andre S. H. Prevot
Atmos. Chem. Phys., 24, 11981–12011, https://doi.org/10.5194/acp-24-11981-2024, https://doi.org/10.5194/acp-24-11981-2024, 2024
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This opinion paper explores how advances in aerosol science inform our understanding of the health impacts of outdoor particulate pollution. We advocate for a shift in the way we target PM pollution, focusing on the most harmful anthropogenic emissions. We highlight key observations, modelling developments, and emission measurements needed to achieve this shift.
Pramod Kumar, Khushboo Sharma, Ankita Malu, Rajeev Rajak, Aparna Gupta, Bidyutjyoti Baruah, Shailesh Yadav, Thupstan Angchuk, Jayant Sharma, Rakesh Kumar Ranjan, Anil Kumar Misra, and Nishchal Wanjari
Atmos. Chem. Phys., 24, 11585–11601, https://doi.org/10.5194/acp-24-11585-2024, https://doi.org/10.5194/acp-24-11585-2024, 2024
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This work monitors and assesses air pollution, especially black and brown carbon, its controlling factor, and its effect on the environment of Sikkim Himalayan region. The huge urban sprawl in recent decades has led to regional human-induced air pollution in the region. Black carbon was highest in April 2021 and March 2022, exceeding the WHO limit. The monsoon season causes huge rainfall over the region, which reduces the pollutants by scavenging (rainout and washout).
Maria P. Velásquez-García, K. Santiago Hernández, James A. Vergara-Correa, Richard J. Pope, Miriam Gómez-Marín, and Angela M. Rendón
Atmos. Chem. Phys., 24, 11497–11520, https://doi.org/10.5194/acp-24-11497-2024, https://doi.org/10.5194/acp-24-11497-2024, 2024
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In the Aburrá Valley, northern South America, local emissions determine air quality conditions. However, we found that external sources, such as regional fires, Saharan dust, and volcanic emissions, increase particulate concentrations and worsen chemical composition by introducing elements like heavy metals. Dry winds and source variability contribute to seasonal influences on these events. This study assesses the air quality risks posed by such events, which can affect broad regions worldwide.
Diana L. Pereira, Chiara Giorio, Aline Gratien, Alexander Zherebker, Gael Noyalet, Servanne Chevaillier, Stéphanie Alage, Elie Almarj, Antonin Bergé, Thomas Bertin, Mathieu Cazaunau, Patrice Coll, Ludovico Di Antonio, Sergio Harb, Johannes Heuser, Cécile Gaimoz, Oscar Guillemant, Brigitte Language, Olivier Lauret, Camilo Macias, Franck Maisonneuve, Bénédicte Picquet-Varrault, Raquel Torres, Sylvain Triquet, Pascal Zapf, Lelia Hawkins, Drew Pronovost, Sydney Riley, Pierre-Marie Flaud, Emilie Perraudin, Pauline Pouyes, Eric Villenave, Alexandre Albinet, Olivier Favez, Robin Aujay-Plouzeau, Vincent Michoud, Christopher Cantrell, Manuela Cirtog, Claudia Di Biagio, Jean-François Doussin, and Paola Formenti
EGUsphere, https://doi.org/10.5194/egusphere-2024-3015, https://doi.org/10.5194/egusphere-2024-3015, 2024
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In order to study aerosols in environments influenced by anthropogenic and biogenic emissions, we performed analysis of samples collected during ACROSS (Atmospheric Chemistry Of the Suburban Forest) campaign in the summer 2022 in the Paris greater area. After analysis of the chemical composition by means of total carbon determination and high resolution mass spectrometry, this work highlights the influence of anthropogenic inputs into the chemical composition of both urban and forested areas.
Meng Wang, Qiyuan Wang, Steven Sai Hang Ho, Jie Tian, Yong Zhang, Shun-cheng Lee, and Junji Cao
Atmos. Chem. Phys., 24, 11175–11189, https://doi.org/10.5194/acp-24-11175-2024, https://doi.org/10.5194/acp-24-11175-2024, 2024
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We studied nitrogen-containing organic compounds (NOCs) in particulate matter <2.5 µm particles on the southeastern Tibetan Plateau. We found that biomass burning and transboundary transport are the main sources of NOCs in the high-altitude area. Understanding these aerosol sources informs how they add to regional and potentially global climate changes. Our findings could help shape effective environmental policies to enhance air quality and address climate impacts in this sensitive region.
Kimmo Teinilä, Sanna Saarikoski, Henna Lintusaari, Teemu Lepistö, Petteri Marjanen, Minna Aurela, Heidi Hellén, Toni Tykkä, Markus Lampimäki, Janne Lampilahti, Luis Barreira, Timo Mäkelä, Leena Kangas, Juha Hatakka, Sami Harni, Joel Kuula, Jarkko V. Niemi, Harri Portin, Jaakko Yli-Ojanperä, Ville Niemelä, Milja Jäppi, Katrianne Lehtipalo, Joonas Vanhanen, Liisa Pirjola, Hanna E. Manninen, Tuukka Petäjä, Topi Rönkkö, and Hilkka Timonen
EGUsphere, https://doi.org/10.5194/egusphere-2024-2235, https://doi.org/10.5194/egusphere-2024-2235, 2024
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Physical and chemical properties of particulate matter and concentrations of trace gases were measured in a street canyon in Helsinki, Finland and an urban background site in January–February 2022 to investigate the effect of wintertime conditions on pollutants. State-of-the-art instruments, a mobile laboratory was used, and the measurement data was further analysed with modelling tools like positive matrix factorization (PMF) and pollution detection algorithm (PDA).
Jinbo Wang, Jiaping Wang, Yuxuan Zhang, Tengyu Liu, Xuguang Chi, Xin Huang, Dafeng Ge, Shiyi Lai, Caijun Zhu, Lei Wang, Qiaozhi Zha, Ximeng Qi, Wei Nie, Congbin Fu, and Aijun Ding
Atmos. Chem. Phys., 24, 11063–11080, https://doi.org/10.5194/acp-24-11063-2024, https://doi.org/10.5194/acp-24-11063-2024, 2024
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In this study, we found large spatial discrepancies in the physical and chemical properties of black carbon over the Tibetan Plateau (TP). Elevated anthropogenic emissions from low-altitude regions can significantly change the mass concentration, mixing state and chemical composition of black-carbon-containing aerosol in the TP region, further altering its light absorption ability. Our study emphasizes the vulnerability of remote plateau regions to intense anthropogenic influences.
Liyuan Zhou, Qianyun Liu, Christian M. Salvador, Michael Le Breton, Mattias Hallquist, Jian Zhen Yu, Chak K. Chan, and Åsa M. Hallquist
Atmos. Chem. Phys., 24, 11045–11061, https://doi.org/10.5194/acp-24-11045-2024, https://doi.org/10.5194/acp-24-11045-2024, 2024
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Our research on city bus emissions reveals that alternative fuels (compressed natural gas and biofuels) reduce fresh particle emissions compared to diesel. However, all fuels lead to secondary air pollution. Aiming at guiding better environmental policies, we studied 76 buses using advanced emission measurement techniques. This work sheds light on the complex effects of bus fuels on urban air quality, emphasizing the need for comprehensive evaluations of future transportation technologies.
Xu Yang, Fobang Liu, Shuqi Yang, Yuling Yang, Yanan Wang, Jingjing Li, Mingyu Zhao, Zhao Wang, Kai Wang, Chi He, and Haijie Tong
Atmos. Chem. Phys., 24, 11029–11043, https://doi.org/10.5194/acp-24-11029-2024, https://doi.org/10.5194/acp-24-11029-2024, 2024
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A study in the rural North China Plain showed environmentally persistent free radicals (EPFRs) in atmospheric particulate matter (PM), with a notable water-soluble fraction likely from atmospheric oxidation during transport. Significant positive correlations between EPFRs and the water-soluble oxidative potential of PM2.5 were found, primarily attributable to the water-soluble fractions of EPFRs. These findings emphasize understanding EPFRs' atmospheric evolution for climate and health impacts.
Genevieve Rose Lorenzo, Luke D. Ziemba, Avelino F. Arellano, Mary C. Barth, Ewan C. Crosbie, Joshua P. DiGangi, Glenn S. Diskin, Richard Ferrare, Miguel Ricardo A. Hilario, Michael A. Shook, Simone Tilmes, Jian Wang, Qian Xiao, Jun Zhang, and Armin Sorooshian
EGUsphere, https://doi.org/10.5194/egusphere-2024-2604, https://doi.org/10.5194/egusphere-2024-2604, 2024
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Novel aerosol hygroscopicity analysis of CAMP2Ex field campaign data show low aerosol hygroscopicity values in Southeast Asia. Organic carbon from smoke decreases hygroscopicity to levels more like those in continental than in polluted marine regions. Hygroscopicity changes at cloud level demonstrate how surface particles impact clouds in the region affecting model representation of aerosol and cloud interactions in similar polluted marine regions with high organic carbon emissions.
Kirsten N. Fossum, Chunshui Lin, Niall O'Sullivan, Lu Lei, Stig Hellebust, Darius Ceburnis, Aqeel Afzal, Anja Tremper, David Green, Srishti Jain, Steigvilė Byčenkienė, Colin O'Dowd, John Wenger, and Jurgita Ovadnevaite
Atmos. Chem. Phys., 24, 10815–10831, https://doi.org/10.5194/acp-24-10815-2024, https://doi.org/10.5194/acp-24-10815-2024, 2024
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The chemical composition and sources of submicron aerosol in the Dublin Port area were investigated over a month-long campaign. Two distinct types of ship emissions were identified and characterised: sulfate-rich plumes from the use of heavy fuel oil with scrubbers and organic-rich plumes from the use of low-sulfur fuels. The latter were more frequent, emitting double the particle number and having a typical V / Ni ratio for ship emission.
Lise Le Berre, Brice Temime-Roussel, Grazia Maria Lanzafame, Barbara D’Anna, Nicolas Marchand, Stéphane Sauvage, Marvin Dufresne, Liselotte Tinel, Thierry Leonardis, Joel Ferreira de Brito, Alexandre Armengaud, Grégory Gille, Ludovic Lanzi, Romain Bourjot, and Henri Wortham
EGUsphere, https://doi.org/10.5194/egusphere-2024-2903, https://doi.org/10.5194/egusphere-2024-2903, 2024
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A summer campaign in a Mediterranean port examined pollution caused by ships. Two stations in the port measured pollution levels and captured over 350 ship plumes to study their chemical composition. Results showed that pollution levels, like ultra-fine particles, were higher in the port than in the city and offer a strong support to improve emission inventories. These findings may also serve as reference for assessing the benefits of a Sulphur Emission Control Area in the Mediterranean in 2025.
Xiao He, Xuan Zheng, Shuwen Guo, Lewei Zeng, Ting Chen, Bohan Yang, Shupei Xiao, Qiongqiong Wang, Zhiyuan Li, Yan You, Shaojun Zhang, and Ye Wu
Atmos. Chem. Phys., 24, 10655–10666, https://doi.org/10.5194/acp-24-10655-2024, https://doi.org/10.5194/acp-24-10655-2024, 2024
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This study introduces an innovative method for identifying and quantifying complex organic vapors and aerosols. By combining advanced analytical techniques and new algorithms, we categorized thousands of compounds from heavy-duty diesel vehicles and ambient air and highlighted specific tracers for emission sources. The innovative approach enhances peak identification, reduces quantification uncertainties, and offers new insights for air quality management and atmospheric chemistry.
Emmanuel Chevassus, Kirsten N. Fossum, Darius Ceburnis, Lu Lei, Chunshui Lin, Wei Xu, Colin D. O’ Dowd, and Jurgita Ovadnevaite
EGUsphere, https://doi.org/10.5194/egusphere-2024-2890, https://doi.org/10.5194/egusphere-2024-2890, 2024
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This study presents the first source apportionment of OA at Mace Head via high-resolution mass spectrometry. Introducing transfer entropy as a novel method reveals that aged OA originate from open ocean ozonolysis and local peat burning oxidation. Methanesulphonic acid OA and primary marine OA both mirror phytoplankton activity as observed with their chemical makeup, with MSA-OA closely tied to coccolithophore blooms and PMOA linked to diatoms, chlorophytes, and cyanobacteria.
Yu Xu, Tang Liu, Yi-Jia Ma, Qi-Bin Sun, Hong-Wei Xiao, Hao Xiao, Hua-Yun Xiao, and Cong-Qiang Liu
Atmos. Chem. Phys., 24, 10531–10542, https://doi.org/10.5194/acp-24-10531-2024, https://doi.org/10.5194/acp-24-10531-2024, 2024
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This study investigates the characteristics of aminiums and ammonium in PM2.5 on clean and polluted winter days in 11 Chinese cities, highlighting the possibility of the competitive uptake of ammonia versus amines on acidic aerosols or the displacement of aminiums by ammonia under high-ammonia conditions. The overall results deepen the understanding of the spatiotemporal differences in aminium characteristics and formation in China.
Cassidy Soloff, Taiwo Ajayi, Yonghoon Choi, Ewan C. Crosbie, Joshua P. DiGangi, Glenn S. Diskin, Marta A. Fenn, Richard A. Ferrare, Francesca Gallo, Johnathan W. Hair, Miguel Ricardo A. Hilario, Simon Kirschler, Richard H. Moore, Taylor J. Shingler, Michael A. Shook, Kenneth L. Thornhill, Christiane Voigt, Edward L. Winstead, Luke D. Ziemba, and Armin Sorooshian
Atmos. Chem. Phys., 24, 10385–10408, https://doi.org/10.5194/acp-24-10385-2024, https://doi.org/10.5194/acp-24-10385-2024, 2024
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Using aircraft measurements over the northwestern Atlantic between the US East Coast and Bermuda and trajectory modeling of continental outflow, we identify trace gas and particle properties that exhibit gradients with offshore distance and quantify these changes with high-resolution measurements of concentrations and particle chemistry, size, and scattering properties. This work furthers our understanding of the complex interactions between continental and marine environments.
Alex Rowell, James Brean, David C. S. Beddows, Zongbo Shi, Avinash Kumar, Matti Rissanen, Miikka Dal Maso, Peter Mettke, Kay Weinhold, Maik Merkel, and Roy M. Harrison
Atmos. Chem. Phys., 24, 10349–10361, https://doi.org/10.5194/acp-24-10349-2024, https://doi.org/10.5194/acp-24-10349-2024, 2024
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Ions enhance the formation and growth rates of new particles, affecting the Earth's radiation budget. Despite these effects, there is little published data exploring the sources of ions in the urban environment and their role in new particle formation (NPF). Here we show that natural ion sources dominate in urban environments, while traffic is a secondary source. Ions contribute up to 12.7 % of the formation rate of particles, indicating that they are important for forming urban PM.
Yuan Cheng, Xu-bing Cao, Sheng-qiang Zhu, Zhi-qing Zhang, Jiu-meng Liu, Hong-liang Zhang, Qiang Zhang, and Ke-bin He
Atmos. Chem. Phys., 24, 9869–9883, https://doi.org/10.5194/acp-24-9869-2024, https://doi.org/10.5194/acp-24-9869-2024, 2024
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The agreement between observational and modeling results is essential for the development of efficient air pollution control strategies. Here we constrained the modeling results of carbonaceous aerosols by field observation in Northeast China, a historically overlooked but recently targeted region of national clean-air actions. Our study suggested that the simulation of agricultural fire emissions and secondary organic aerosols remains challenging.
Yuan Dai, Junfeng Wang, Houjun Wang, Shijie Cui, Yunjiang Zhang, Haiwei Li, Yun Wu, Ming Wang, Eleonora Aruffo, and Xinlei Ge
Atmos. Chem. Phys., 24, 9733–9748, https://doi.org/10.5194/acp-24-9733-2024, https://doi.org/10.5194/acp-24-9733-2024, 2024
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Short-term strict emission control can improve air quality, but its effectiveness needs assessment. During the 2021 summer COVID-19 lockdown in Yangzhou, we found that PM2.5 levels did not decrease despite reduced primary emissions. Aged black-carbon particles increased substantially due to higher O3 levels and transported pollutants. High humidity and low wind also played key roles. The results highlight the importance of a regionally balanced control strategy for future air quality management.
Xinya Liu, Diego Alves Gouveia, Bas Henzing, Arnoud Apituley, Arjan Hensen, Danielle van Dinther, Rujin Huang, and Ulrike Dusek
Atmos. Chem. Phys., 24, 9597–9614, https://doi.org/10.5194/acp-24-9597-2024, https://doi.org/10.5194/acp-24-9597-2024, 2024
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The vertical distribution of aerosol optical properties is important for their effect on climate. This is usually measured by lidar, which has limitations, most notably the assumption of a lidar ratio. Our study shows that routine surface-level aerosol measurements are able to predict this lidar ratio reasonably well within the lower layers of the atmosphere and thus provide a relatively simple and cost-effective method to improve lidar measurements.
Weiqi Xu, Ye Kuang, Wanyun Xu, Zhiqiang Zhang, Biao Luo, Xiaoyi Zhang, Jiangchuang Tao, Hongqin Qiao, Li Liu, and Yele Sun
Atmos. Chem. Phys., 24, 9387–9399, https://doi.org/10.5194/acp-24-9387-2024, https://doi.org/10.5194/acp-24-9387-2024, 2024
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We deployed an advanced aerosol–fog sampling system at a rural site in the North China Plain to investigate impacts of aerosol hygroscopic growth and activation on the physicochemical properties of submicron aerosols. Observed results highlighted remarkably different aqueous processing of primary and secondary submicron aerosol components under distinct ambient relative humidity (RH) conditions and that RH levels significantly impact aerosol sampling through the aerosol swelling effect.
Can Wu, Xiaodi Liu, Ke Zhang, Si Zhang, Cong Cao, Jianjun Li, Rui Li, Fan Zhang, and Gehui Wang
Atmos. Chem. Phys., 24, 9263–9275, https://doi.org/10.5194/acp-24-9263-2024, https://doi.org/10.5194/acp-24-9263-2024, 2024
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Brown carbon (BrC) is prevalent in the troposphere and can efficiently absorb solar and terrestrial radiation. Our observations show that the enhanced light absorption of BrC relative to black carbon at the tropopause can be attributed to the formation of nitrogen-containing organic compounds through the aqueous-phase reactions of carbonyls with ammonium.
Cited articles
Aarons, S. M., Aciego, S. M., Gabrielli, P., Delmonte, B., Koornneef, J. M.,
Wegner, A., and Blakowski, M. A.: The impact of glacier retreat from the
Ross Sea on local climate: Characterization of mineral dust in the Taylor
Dome ice core, East Antarctica, Earth Planet. Sci. Lett., 444,
34–44, https://doi.org/10.1016/j.epsl.2016.03.035, 2016.
Albani, S., Mahowald, N., Delmonte, B., Maggi, V., and Winckler, G.:
Comparing modeled and observed changes in mineral dust transport and
deposition to Antarctica between the Last Glacial Maximum and current
climates, Clim. Dynam., 38, 1731–1755,
https://doi.org/10.1007/s00382-011-1139-5, 2012.
Andreae, M. O. and Gelencsér, A.: Black carbon or brown carbon? The
nature of light-absorbing carbonaceous aerosols, Atmos. Chem. Phys.,
6, 3131–3148, https://doi.org/10.5194/acp-6-3131-2006, 2006.
Aoki, T., Kuchiki, K., Niwano, M., Kodama, Y., Hosaka, M., and Tanaka, T.:
Physically based snow albedo model for calculating broadband albedos and the
solar heating profile in snowpack for general circulation models, J.
Geophys. Res., 116, D11114, https://doi.org/10.1029/2010JD015507, 2011.
Arienzo, M., McConnell, J., Murphy, L., Chellman, N., Das, S., Kipfstuhl,
S., and Mulvaney, R.: Holocene black carbon in Antarctica paralleled
Southern Hemisphere climate, J. Geophys. Res.-Atmos., 122, 6713–6728,
https://doi.org/10.1002/2017JD026599, 2017.
Bisiaux, M. M., Edwards, R., McConnell, J. R., Curran, M. A. J., Van Ommen,
T. D., Smith, A. M., Neumann, T. A., Pasteris, D. R., Penner, J. E., and
Taylor, K.: Changes in black carbon deposition to Antarctica from two
high-resolution ice core records, 1850–2000 AD, Atmos. Chem. Phys., 12,
4107–4115, https://doi.org/10.5194/acp-12-4107-2012, 2012.
Bodhaine, B. A.: Aerosol absorption measurements at Barrow, Mauna Loa and
the South Pole, J. Geophys. Res.-Atmos. (1984–2012),
100, 8967–8975, https://doi.org/10.1029/95JD00513, 1995.
Bond, T. C, Doherty, S. J., Fahey, D. W., Forster, P. M., Berntsen, T.,
DeAngelo, B. J., Flanner, M. G., Ghan, S., Kärcher, B., Koch, D., Kinne,
S., Kondo, Y., Quinn, P. K., Sarofim, M. C., Schultz, M. G., Schulz, M.,
Venkataraman, C., Zhang, H., Zhang, S., Bellouin, N., Guttikunda, S. K.,
Hopke, R. K., Jacobson, M. Z., Kaiser, J. W., Klimont, Z., Lohmann, U.,
Schwarz, J. P., Shindell, D., Storelvmo, T., Warren, S. G., and Zender, C.
S.: Bounding the role of black carbon in the climate system: A scientific
assessment, J. Geophys. Res.-Atmos., 118, 5380–5552,
https://doi.org/10.1002/jgrd.50171, 2013.
Bory, A., Wolff, E., Mulvaney, R., Jagoutz, E., Wegner, A., Ruth, U., and
Elderfield, H.: Multiple sources supply eolian mineral dust to the Atlantic
sector of coastal Antarctica: Evidence from recent snow layers at the top of
Berkner Island ice sheet, Earth Planet. Sci. Lett., 291,
138–148, https://doi.org/10.1016/j.epsl.2010.01.006, 2010.
Chang, C., Han, C., Han, Y., Hur, S., Lee, S., Motoyama, H., Hou, S., and
Hong, S.: Persistent Pb pollution in central East Antarctic snow: a
retrospective assessment of sources and control policy implications,
Environ. Sci. Technol., 50, 12138–12145,
https://doi.org/10.1021/acs.est.6b03209, 2016.
Chaubey, J., Moorthy, B., Nair, V., and Tiwari, A.: Black carbon aerosols
over coastal Antarctica and its scavenging by snow during the Southern
Hemispheric summer, J. Geophys. Res., 115, D10210,
https://doi.org/10.1029/2009JD013381, 2010.
Collaud Coen, M., Weingartner, E., Apituley, A., Ceburnis, D.,
Fierz-Schmidhauser, R., Flentje, H., Henzing, J. S., Jennings, S. G.,
Moerman, M., Petzold, A., Schmid, O., and Baltensperger, U.: Minimizing light
absorption measurement artifacts of the Aethalometer: evaluation of five
correction algorithms, Atmos. Meas. Tech., 3, 457–474,
https://doi.org/10.5194/amt-3-457-2010, 2010.
De Deckker, P., Norman, M., Goodwin, I., Wain, A., and Gingele, F.: Lead
isotopic evidence for an Australian source of aeolian dust to Antarctica at
times over the last 170,000 years, Palaeogeogr. Palaeoclim.
Palaeoecol., 285, 205–223, https://doi.org/10.1016/j.palaeo.2009.11.013, 2010.
Delmonte, B., Petit, J. R., Andersen, P. S., Basile-Doelsch, I., Maggi, V.,
and Lipenkov, V.: Dust size evidence for opposite regional atmospheric
circulation changes over east Antarctica during the last climatic
transition, Clim. Dynam., 23, 427–438, https://doi.org/10.1007/s00382-004-0450-9, 2004.
Delmonte, B., Andersson, P. S., Hansson, M., Schöberg, H., Petit, J. R.,
Basile-Doelsch, I., and Maggi, V.: Aeolian dust in East Antarctica
(EPICA-Dome C and Vostok): Provenance during glacial ages over the last 800
kyr, Geophys. Res. Lett., 35, L07703, https://doi.org/10.1029/2008GL033382, 2008.
Edwards, D. P., Emmons, L. K., Gille, J. C., Chu, A., Attié, J.-L.,
Giglio, L., Wood, S. W., Haywood, J., Deeter, M. N., Massie, S. T., Ziskin,
D. C., and Drummond, J. R.: Satellite-observed pollution from Southern
Hemisphere biomass burning, J. Geophys. Res., 111, D14312,
https://doi.org/10.1029/2005JD006655, 2006a.
Edwards, D. P., Pétron, G., Novelli, P., Emmons, L., Gille, J. C., and
Drummond, J. R.: Southern Hemisphere carbon monoxide interannual variability
observed by Terra/Measurement of Pollution in the Troposphere (MOPITT),
J. Geophys. Res., 111, D16303, https://doi.org/10.1029/2006JD007079,
2006b.
Evangelista, H., Maldonado, J., Godoi, R. H. M.,, Pereira, E. B., Koch, D.,
Tanizaki-Fonseca, K., Grieken, V., R., Sampaio, M., Setzer, A., Alencar, A.,
and Gonçalves, S. C.: Sources and transport of urban and biomass burning
aerosol black carbon at the South-West Atlantic Coast, J.
Atmos. Chem., 56, 225–238, https://doi.org/10.1007/s10874-006-9052-8, 2007.
Fiebig, M., Lunder C. R., and Stohl, A.: Tracing biomass burning aerosol
from South America to Troll Research Station, Antarctica, Geophys.
Res. Lett., 36, L14815, https://doi.org/10.1029/2009GL038531, 2009.
Flanner, M., Zender, C., Randerson, J., and Rasch, P.: Present-day climate
forcing and response from black carbon in snow, J. Geophys.
Res., 112, D11202, https://doi.org/10.1029/2006JD008003, 2007.
Gabrielli, P., Wegner, A., Petit, J., Delmonte, B., Deckker, P., Gaspari,
V., Fischer, H., Ruth, U., Kriews, M., Boutron, C., Cescon, P., and
Barbante, C.: A major glacial-interglacial change in aeolian dust
composition inferred from Rare Earth Elements in Antarctic ice, Quaternary
Sci. Rev., 29, 265–273,
https://doi.org/10.1016/j.quascirev.2009.09.002, 2010.
Gambaro, A., Zangrando, R., Gabrielli, P., Barbante, C., and Cescon, P.:
Direct determination of levoglucosan at the picogram per milliliter level in
Antarctic ice by high-performance liquid chromatography/electrospray
ionization triple quadrupole mass spectrometry, Anal. Chem., 80,
1649–1655, https://doi.org/10.1021/ac701655x, 2008.
Gassó, S., Stein, A., Marino, F., Castellano, E., Udisti, R.,
and Ceratto, J.: A combined observational and modeling approach
to study modern dust transport from the Patagonia desert to East
Antarctica, Atmos. Chem. Phys., 10, 8287–8303, https://doi.org/10.5194/acp-10-8287-2010, 2010.
Gelencsér, A: Chapter 3: Major carbonaceous particle types and their
sources in “Carbonaceous aerosol”, 45–147, Springer, 2004.
Giglio, L., Randerson, J., and Werf, G.: Analysis of daily, monthly, and
annual burned area using the fourth-generation global fire emissions
database (GFED4), J. Geophys. Res.-Biogeosci., 118,
317–328, https://doi.org/10.1002/jgrg.20042, 2013.
Gilardoni, S. and Fuzzi, S., Chemical composition of aerosols of different
origin in “Atmospheric aerosols: Life cycles and effects on air quality and
climate” edited by Tomasi, C., Fuzzi, S., and Kokhanovsky, A., 183-221,
Wiley-VCH, 2017.
Gili, S., Gaiero, D., Goldstein, S., Chemale, F., Koester, E., Jweda, J.,
Vallelonga, P., and Kaplan, M.: Provenance of dust to Antarctica: A lead
isotopic perspective, Geophys. Res. Lett., 43, 2291–2298,
https://doi.org/10.1002/2016GL068244, 2016.
Graf, H.-F., Shirsat, S. V., Oppenheimer, C., Jarvis, M. J., Podzun, R., and
Jacob, D.: Continental scale Antarctic deposition of sulphur and black carbon
from anthropogenic and volcanic sources, Atmos. Chem. Phys., 10, 2457–2465,
https://doi.org/10.5194/acp-10-2457-2010, 2010.
Gros, V., Bonsang, B., Martin, D., Novelli, P. C., and Kazan, V.:
Carbon monoxide short term measurements at Amsterdam island:
estimations of biomass
burning emission rates, Chemosphere – Global Change Sci., 1,
163–172, https://doi.org/10.1016/S1465-9972(99)00009-4, 1999.
Hadley, O. and Kirchstetter, T.: Black-carbon reduction of snow albedo, Nat.
Clim. Change, 2, 437–440, https://doi.org/10.1038/nclimate1433, 2012.
Hagler, G. S. W., Bergin, M. H., Smith, E. A., Town, M., and Dibb, J. E.:
Local anthropogenic impact on particulate elemental carbon concentrations at
Summit, Greenland, Atmos. Chem. Phys., 8, 2485–2491,
https://doi.org/10.5194/acp-8-2485-2008, 2008.
Hansen, A. D. A., Bodhaine, B. A., Dutton, E. G., and Schnell, R. C.: Aerosol
black carbon measurements at the South Pole: Initial results, 1986–1987,
Geophys. Res. Lett., 15, 1193-1196, https://doi.org/10.1029/GL015i011p01193, 1988.
Hansen, A., Lowenthal, D., Chow, J., and Watson, J.: Black carbon aerosol at
McMurdo station, Antarctica, J. Air Waste Manage.
Assoc., 51, 593–600, https://doi.org/10.1080/10473289.2001.10464283, 2001.
Hara, K., Kikuchi, T., Furuya, K., Hayashi, M., and Fujii, Y.:
Characterization of Antarctic aerosol particles using laser microprobe mass
spectrometry, Environ. Sci. Techno., 30, 385–391,
https://doi.org/10.1021/es9407305, 1996.
Hara, K., Osada, K., Yabuki, M., Hashida, G., Yamanouchi, T., Hayashi, M.,
Shiobara, M., Nishita, C., and Wada, M.: Haze episodes at Syowa Station,
coastal Antarctica: Where did they come from?, J. Geophys.
Res., 115, D14205,
https://doi.org/10.1029/2009JD012582, 2010.
Hara, K., Osada, K., Nishita-Hara, C., Yabuki, M., Hayashi,
M., Yamanouchi, T., Wada, M., and Shiobara, M.: Seasonal
features of ultrafine particle volatility in the coastal
Antarctic troposphere, Atmos. Chem. Phys., 11, 9803–9812,
https://doi.org/10.5194/acp-11-9803-2011, 2011.
Hara, K., Osada, K., and Yamanouchi, T.: Tethered balloon-borne aerosol
measurements: seasonal and vertical variations of aerosol constituents over
Syowa Station, Antarctica, Atmos. Chem. Phys., 13, 9119–9139,
https://doi.org/10.5194/acp-13-9119-2013, 2013.
Hu, Q.-H., Xie, Z.-Q., Wang, X.-M., Kang, H., and Zhang, P.: Levoglucosan
indicates high levels of biomass burning aerosols over oceans from the
Arctic to Antarctic, Sci. Rep., 3, 3119, https://doi.org/10.1038/srep03119,
2013.
Ito, A., Ito, A., and Akimoto, H.: Seasonal and interannual variations in CO
and BC emissions from open biomass burning in Southern Africa during
1998–2005, Global Biogeochem. Cy., 21, GB2011, https://doi.org/10.1029/2006GB002848, 2007.
Krinner, G., Petit, J.-R., and Delmonte: Altitude of atmospheric tracer
transport towards Antarctica in present and glacial climate, Quaternary
Sci. Rev., 29, 274–284, https://doi.org/10.1016/j.quascirev.2009.06.020, 2010.
Li, F., Ginoux, P., and Ramaswamy, V.: Transport of Patagonian dust to
Antarctica, J. Geophys. Res.-Atmos. (1984–2012),
115, D18217, https://doi.org/10.1029/2009JD012356, 2010.
Minikin, A., Legrand, M., Hall, J., Wagenbach, D., Kleefeld, C., Wolff, E.,
Pasteur, E., and Ducroz, F.: Sulfur-containing species (sulfate and
methanesulfonate) in coastal Antarctic aerosol and precipitation, J.
Geophys. Res., 103, 10975–10990, https://doi.org/10.1029/98JD00249, 1998.
Moorthy, K. K., Satheesh, S. K., Babu, S. S. and Saha, A.:
Large latitudinal
gradients and temporal heterogeneity in aerosol black
carbon and its mass
mixing ratio over southern and northern oceans observed during a
trans-continental cruise experiment, Geophys. Res. Lett., 32,
L14818, https://doi.org/10.1029/2005GL023267, 2005.
Moschos, V., Kumar, N., Daellenbach, K., Baltensperger, U., Prevot, A., and
Haddad, I.: Source Apportionment of Brown Carbon Absorption by Coupling
UV/Vis Spectroscopy with Aerosol Mass Spectrometry, Environ. Sci. Technol.
Lett., 5, 302–308, https://doi.org/10.1021/acs.estlett.8b00118, 2018.
Moteki, N., Adachi, K., Ohata, S., Yoshida, A., Harigaya, T., Koike, M., and
Kondo, Y.: Anthropogenic iron oxide aerosols enhance atmospheric heating,
Nat. Commun., 8, 15329, https://doi.org/10.1038/ncomms15329, 2017.
Myhre, C. E., D'Anna, B., Nicolaisen, F. M., and Nielsen, C. J.: Properties
of aqueous methanesulfonic acid: complex index of refraction and surface
tension, Appl. Opt., 43, 2500–2509, 2004.
Neff, P. and Bertler, N.: Trajectory modeling of modern dust transport to
the Southern Ocean and Antarctica, J. Geophys. Res.-Atmos.,
120, 9303–9322, https://doi.org/10.1002/2015JD023304, 2015.
Novakov, T.: The role of soot and primary oxidants in atmospheric chemistry,
Sci. Total Environ., 36, 1–10,
https://doi.org/10.1016/0048-9697(84)90241-9, 1984.
Pasteris, D., McConnell, J., Das, S., Criscitiello, A., Evans, M., Maselli,
O., Sigl, M., and Layman, L.: Seasonally resolved ice core records from West
Antarctica indicate a sea ice source of sea salt aerosol and a biomass
burning source of ammonium, J. Geophys. Res.-Atmos., 119, 9168–9182,
https://doi.org/10.1002/2013JD020720, 2014.
Pereira, E., Evangelista, H., Pereira, K., Cavalcanti, I., and Setzer, A.:
Apportionment of black carbon in the South Shetland Islands, Antarctic
Peninsula, J. Geophys. Res.-Atmos. (1984–2012),
111, D03303, https://doi.org/10.1029/2005JD006086, 2006.
Pereira, K., Evanhelista, H., Pereira, E., Simões, J., Johnson, E., and
Melo, L.: Transport of crustal microparticles from Chilean Patagonia to the
Antarctic Peninsula by SEM-EDS analysis, Tellus B, 56, 262–275,
https://doi.org/10.1111/j.1600-0889.2004.00105.x, 2004.
Planchon, F., Boutron, C., Barbante, C., Cozzi, G., Gaspari, V., Wolff, E.,
Ferrari, C., and Cescon, P.: Changes in heavy metals in Antarctic snow from
Coats Land since the mid-19th to the late 20th century, Earth Planet.
Sci. Lett., 200, 207–222, https://doi.org/10.1016/S0012-821X(02)00612-X, 2002.
Preunkert, S., Jourdain, B., Legrand, M., Udisti, R., Becagli, S., and
Cerri, O.: Seasonality of sulfur species (dimethyl sulfide, sulfate, and
methanesulfonate) in Antarctica: Inland versus coastal regions, J.
Geophys. Res., 113, D15302, https://doi.org/10.1029/2008JD009937, 2008.
Sakerin, S. M., Smirnov, A., Kabanov, D. M., Pol'kin, V. V., Panchenko, M.
V., Holben, B. N., and Kopelevich, O. V.: Aerosol optical and microphysical
properties over the Atlantic Ocean during the 19th Cruise of the Research
Vessel Akademik Sergey Vavilov, J. Geophys. Res., 112, D10220,
https://doi.org/10.1029/2006JD007947, 2007.
Saleh, R., Hennigan, C. J., McMeeking, G. R., Chuang, W. K., Robinson,
E. S., Coe, H., Donahue, N. M., and Robinson, A. L.: Absorptivity of
brown carbon in fresh and photo-chemically aged biomass-burning
emissions, Atmos. Chem. Phys., 13, 7683–7693, https://doi.org/10.5194/acp-13-7683-2013, 2013.
Saleh, R., Robinson, E., Tkacik, D., Ahern, A., Liu, S., Aiken, A.,
Sullivan, R., Presto, A., Dubey, M., Yokelson, R., Donahue, N., and
Robinson, A.: Brownness of organics in aerosols from biomass burning linked
to their black carbon content, Nat. Geosci., 7, 647–650,
https://doi.org/10.1038/ngeo2220, 2014.
Schwarz, J. P., Samset, B. H., Perring, A. E., Spackman, J. R., Gao, R. S.,
Stier, P., Schulz, M., Moore, F. L., Ray, E. A., and Fahey, D. W.:
Global-scale seasonally resolved black carbon vertical profiles over the
Pacific, Geophys. Res. Lett., 40, 5542–5547, https://doi.org/10.1002/2013GL057775, 2013.
Sciare, J., Favez, O., Sarda-Estève, R., Oikonomou, K.,
Cachier, H., and Kazan, V.: Long-term observations of carbonaceous
aerosols in the Austral Ocean atmosphere: Evidence of a biogenic
marine organic source, J. Geophys. Res., 114, D15302,
https://doi.org/10.1029/2009JD011998, 2009.
Sharma, S., Leaitch, W. R., Huang, L., Veber, D., Kolonjari, F., Zhang, W.,
Hanna, S. J., Bertram, A. K., and Ogren, J. A.: An evaluation of three
methods for measuring black carbon in Alert, Canada, Atmos. Chem. Phys., 17,
15225–15243, https://doi.org/10.5194/acp-17-15225-2017, 2017.
Shiraiwa, M., Kondo, Y., Moteki, N., Takegawa, N., Miyazaki, Y., and Blake,
D. R.: Evolution of mixing state of black carbon in polluted air from Tokyo,
Geophys. Res. Lett., 34, L16803, https://doi.org/10.1029/2007GL029819, 2007.
Shirsat, S. V. and Graf, H. F.: An emission inventory of sulfur from
anthropogenic sources in Antarctica, Atmos. Chem. Phys.,
9, 3397–3408, https://doi.org/10.5194/acp-9-3397-2009, 2009.
Smith, J., Vance, D., Kemp, R., Archer, C., Toms, P., King, M., and
Zárate, M.: Isotopic constraints on the source of Argentinian loess –
with implications for atmospheric circulation and the provenance of
Antarctic dust during recent glacial maxima, Earth Planet. Sci.
Lett., 212, 181–196, https://doi.org/10.1016/S0012-821X(03)00260-7, 2003.
Stein, A. F., Draxler, R. R, Rolph, G. D., Stunder, B. J. B., Cohen, M. D.,
and Ngan, F.: NOAA's HYSPLIT atmospheric transport and dispersion modeling
system, B. Am. Meteorol. Soc., 96, 2059–2077, https://doi.org/10.1175/BAMS-D-14-00110.1, 2015.
Stohl, A. and Sodemann, H.: Characteristics of atmospheric transport into
the Antarctic troposphere, J. Geophys. Res., 115, D02305,
https://doi.org/10.1029/2009JD012536, 2010.
Sudo, K. and Akimoto, H.: Global source attribution of tropospheric ozone:
Long-range transport from various source regions, J. Geophys. Res., 112,
D12302, https://doi.org/10.1029/2006JD007992, 2007.
Sudo, K., Takahashi, M., Kurokawa, J., and Akimoto, H.: Chaser: A global
chemical model of the troposphere, 1. Model description, J. Geophys. Res.,
107, 4339, https://doi.org/10.1029/2001JD001113, 2002.
Takemura, T., Nozawa, T., Emori, S., Nakajima, T. Y., and Nakajima, T.:
Simulation of climate response to aerosol direct and indirect effects with
aerosol transport-radiation model, J. Geophys. Res., 110,
D02202, https://doi.org/10.1029/2004JD005029, 2005.
Tomikawa, Y., Nishimura, Y. and Yamanouchi, T.: Characteristics of
Tropopause and Tropopause Inversion Layer in the Polar Region, SOLA,
5, 141–144, https://doi.org/10.2151/sola.2009-036, 2009.
Torres, O., Chen, Z., Jethva, H., Ahn, C., Freitas, S. R., and Bhartia,
P. K.: OMI and MODIS observations of the anomalous 2008–2009
Southern Hemisphere biomass burning seasons, Atmos. Chem. Phys., 10,
3505–3513, https://doi.org/10.5194/acp-10-3505-2010, 2010.
Ueda, S., Osada, K., Hara, K., Yabuki, M., Hashihama, F., and Kanda, J.:
Morphological features and mixing states of soot-containing particles in the
marine boundary layer over the Indian and Southern oceans, Atmos. Chem.
Phys., 18, 9207–9224, https://doi.org/10.5194/acp-18-9207-2018, 2018.
Vallelonga, P., Velde, K., Candelone, J.-P., Morgan, V. Boutron, C., and
Rosman, K.: The lead pollution history of Law Dome, Antarctica, from
isotopic measurements of ice cores: 1500 AD to 1989 AD, Earth Planet.
Sci. Lett., 204, 291–306,
https://doi.org/10.1016/S0012-821X(02)00983-4, 2002.
Vallelonga, P., Gabrielli, P., Balliana, E., Wegner, A., Delmonte, B.,
Turetta, C., Burton, G., Vanhaecke, F., Rosman, K. J. R., Hong, S., Boutron,
C. F., Cescon P., and Barbante, C.: Lead isotopic compositions in the EPICA
Dome C ice core and Southern Hemisphere Potential Source Areas, Quaternary
Sci. Rev., 29, 247–255,
https://doi.org/10.1016/j.quascirev.2009.06.019, 2010.
van der Werf, G. R., Randerson, J. T., Giglio, L., Collatz, G. J.,
Kasibhatla, P. S., and Arellano Jr., A. F.: Interannual variability in global
biomass burning emissions from 1997 to 2004, Atmos. Chem. Phys., 6,
3423–3441, https://doi.org/10.5194/acp-6-3423-2006, 2006.
Wagenbach, D.: Coastal Antarctica: atmospheric chemical composition and
atmospheric transport, in: Chemical Exchange Between the Atmosphere and
Polar Snow, NATO ASI Series Volume 43, edited by: Wolff, E. W. and Bales, R. C.,
Springer-Verlag, Berlin Heidelberg, 173–199, 1996.
Warren, S. G. and Clarke, A. D.: Soot in the atmosphere and snow surface of
Antarctica, J. Geophys. Res., 95, 1811–1816, 1990.
Watanabe, S., Hajima, T., Sudo, K., Nagashima, T., Takemura, T., Okajima, H.,
Nozawa, T., Kawase, H., Abe, M., Yokohata, T., Ise, T., Sato, H., Kato, E.,
Takata, K., Emori, S., and Kawamiya, M.: MIROC-ESM 2010: model description
and basic results of CMIP5-20c3m experiments, Geosci. Model Dev., 4, 845–872,
https://doi.org/10.5194/gmd-4-845-2011, 2011.
Wegner, A., Gabrielli, P., Wilhelms-Dick, D., Ruth, U., Kriews, M., De
Deckker, P., Barbante, C., Cozzi, G., Delmonte, B., and Fischer, H.: Change
in dust variability in the Atlantic sector of Antarctica at the end of the
last deglaciation, Clim. Past, 8, 135–147,
https://doi.org/10.5194/cp-8-135-2012, 2012.
Weingartner, E., Saathoff, H., Schnaiter, M., Streit, N., Bitnar, B., and
Baltensperger, U.: Absorption of light by soot particles: determination of
the absorption coefficient by means of aethalometers, J. Aerosol
Sci., 34, 1445–1463, https://doi.org/10.1016/S0021-8502(03)00359-8, 2003.
Weller, R., Wagenbach, D., Legrand, M., Elsnsser, C., Tian-Kunze, X., and
Kónig-Langlo, G.: Continuous 25-yr aerosol records at coastal Antarctica
– I: Interannual variability of ionic compounds and links to climate
indices, Tellus, 63B, 901–919, https://doi.org/10.1111/j.1600-0889.2011.00542.x, 2011.
Weller, R., Minikin, A., Petzold, A., Wagenbach, D., and König-Langlo, G.:
Characterization of long-term and seasonal variations of black carbon (BC)
concentrations at Neumayer, Antarctica, Atmos. Chem. Phys., 13, 1579–1590,
https://doi.org/10.5194/acp-13-1579-2013, 2013.
Wolff, E. and Cachier, H.: Concentrations and seasonal cycle of black carbon
in aerosol at a coastal Antarctic station, J. Geophys. Res.,
103, 11033–11041, https://doi.org/10.1029/97JD01363, 1998.
Zangrando, R., Barbaro, E., Vecchiato, M., Kehrwald, N., Barbante, C., and
Gambaro, A.: Levoglucosan and phenols in Antarctic marine, coastal and
plateau aerosols, Sci. Total Environ., 544, 606–616,
https://doi.org/10.1016/j.scitotenv.2015.11.166, 2016.
Zhang, X., Liu, Z., Hecobian, A., Zheng, M., Frank, N. H., Edgerton, E. S.,
and Weber, R. J.: Spatial and seasonal variations of fine particle
water-soluble organic carbon (WSOC) over the southeastern United States:
implications for secondary organic aerosol formation, Atmos. Chem. Phys., 12,
6593–6607, https://doi.org/10.5194/acp-12-6593-2012, 2012.
Short summary
We measured equivalent black carbon (EBC) concentrations at Syowa Station, Antarctica, from February 2005. EBC might be transported directly to Syowa Station from mid-latitudes mainly via the boundary layer and the lower free troposphere. Some BC was transported to Antarctic regions via the upper free troposphere. Biomass burning in South America and southern Africa is the most dominant source. Fossil fuel combustion in South America and southern Africa also have important contributions.
We measured equivalent black carbon (EBC) concentrations at Syowa Station, Antarctica, from...
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