Articles | Volume 18, issue 19
https://doi.org/10.5194/acp-18-14465-2018
© Author(s) 2018. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Special issue:
https://doi.org/10.5194/acp-18-14465-2018
© Author(s) 2018. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Research article
| 
10 Oct 2018
Research article |
| 10 Oct 2018
| 10 Oct 2018
Atmospheric Δ17O(NO3−) reveals nocturnal chemistry dominates nitrate production in Beijing haze
Pengzhen He
Anhui Province Key Laboratory of Polar Environment and Global Change,
School of Earth and Space Sciences, University of Science and Technology of
China, Hefei, Anhui 230026, China
Zhouqing Xie
CORRESPONDING AUTHOR
Anhui Province Key Laboratory of Polar Environment and Global Change,
School of Earth and Space Sciences, University of Science and Technology of
China, Hefei, Anhui 230026, China
Center for Excellence in Urban Atmospheric Environment, Institute of
Urban Environment, Chinese Academy of Sciences, Xiamen, Fujian 361021,
China
Key Lab of Environmental Optics and Technology, Anhui Institute of
Optics and Fine Mechanics, Chinese Academy of Sciences, Hefei, Anhui 230031,
China
Xiyuan Chi
Anhui Province Key Laboratory of Polar Environment and Global Change,
School of Earth and Space Sciences, University of Science and Technology of
China, Hefei, Anhui 230026, China
Xiawei Yu
Anhui Province Key Laboratory of Polar Environment and Global Change,
School of Earth and Space Sciences, University of Science and Technology of
China, Hefei, Anhui 230026, China
Shidong Fan
Anhui Province Key Laboratory of Polar Environment and Global Change,
School of Earth and Space Sciences, University of Science and Technology of
China, Hefei, Anhui 230026, China
Hui Kang
Anhui Province Key Laboratory of Polar Environment and Global Change,
School of Earth and Space Sciences, University of Science and Technology of
China, Hefei, Anhui 230026, China
Cheng Liu
Anhui Province Key Laboratory of Polar Environment and Global Change,
School of Earth and Space Sciences, University of Science and Technology of
China, Hefei, Anhui 230026, China
Center for Excellence in Urban Atmospheric Environment, Institute of
Urban Environment, Chinese Academy of Sciences, Xiamen, Fujian 361021,
China
Key Lab of Environmental Optics and Technology, Anhui Institute of
Optics and Fine Mechanics, Chinese Academy of Sciences, Hefei, Anhui 230031,
China
Haicong Zhan
Anhui Province Key Laboratory of Polar Environment and Global Change,
School of Earth and Space Sciences, University of Science and Technology of
China, Hefei, Anhui 230026, China
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This study mapped the drivers of HCHO variability from 2015 to 2019 over eastern China. Hydroxyl (OH) radical production rates from HCHO photolysis were evaluated. The relative contributions of emitted and photochemical sources to the observed HCHO abundance were analyzed. Contributions of various emission sources and geographical regions to the observed HCHO summertime enhancements were determined.
Tijl Verhoelst, Steven Compernolle, Gaia Pinardi, Jean-Christopher Lambert, Henk J. Eskes, Kai-Uwe Eichmann, Ann Mari Fjæraa, José Granville, Sander Niemeijer, Alexander Cede, Martin Tiefengraber, François Hendrick, Andrea Pazmiño, Alkiviadis Bais, Ariane Bazureau, K. Folkert Boersma, Kristof Bognar, Angelika Dehn, Sebastian Donner, Aleksandr Elokhov, Manuel Gebetsberger, Florence Goutail, Michel Grutter de la Mora, Aleksandr Gruzdev, Myrto Gratsea, Georg H. Hansen, Hitoshi Irie, Nis Jepsen, Yugo Kanaya, Dimitris Karagkiozidis, Rigel Kivi, Karin Kreher, Pieternel F. Levelt, Cheng Liu, Moritz Müller, Monica Navarro Comas, Ankie J. M. Piters, Jean-Pierre Pommereau, Thierry Portafaix, Cristina Prados-Roman, Olga Puentedura, Richard Querel, Julia Remmers, Andreas Richter, John Rimmer, Claudia Rivera Cárdenas, Lidia Saavedra de Miguel, Valery P. Sinyakov, Wolfgang Stremme, Kimberly Strong, Michel Van Roozendael, J. Pepijn Veefkind, Thomas Wagner, Folkard Wittrock, Margarita Yela González, and Claus Zehner
Atmos. Meas. Tech., 14, 481–510, https://doi.org/10.5194/amt-14-481-2021, https://doi.org/10.5194/amt-14-481-2021, 2021
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This paper reports on the ground-based validation of the NO2 data produced operationally by the TROPOMI instrument on board the Sentinel-5 Precursor satellite. Tropospheric, stratospheric, and total NO2 columns are compared to measurements collected from MAX-DOAS, ZSL-DOAS, and PGN/Pandora instruments respectively. The products are found to satisfy mission requirements in general, though negative mean differences are found at sites with high pollution levels. Potential causes are discussed.
Jan-Lukas Tirpitz, Udo Frieß, François Hendrick, Carlos Alberti, Marc Allaart, Arnoud Apituley, Alkis Bais, Steffen Beirle, Stijn Berkhout, Kristof Bognar, Tim Bösch, Ilya Bruchkouski, Alexander Cede, Ka Lok Chan, Mirjam den Hoed, Sebastian Donner, Theano Drosoglou, Caroline Fayt, Martina M. Friedrich, Arnoud Frumau, Lou Gast, Clio Gielen, Laura Gomez-Martín, Nan Hao, Arjan Hensen, Bas Henzing, Christian Hermans, Junli Jin, Karin Kreher, Jonas Kuhn, Johannes Lampel, Ang Li, Cheng Liu, Haoran Liu, Jianzhong Ma, Alexis Merlaud, Enno Peters, Gaia Pinardi, Ankie Piters, Ulrich Platt, Olga Puentedura, Andreas Richter, Stefan Schmitt, Elena Spinei, Deborah Stein Zweers, Kimberly Strong, Daan Swart, Frederik Tack, Martin Tiefengraber, René van der Hoff, Michel van Roozendael, Tim Vlemmix, Jan Vonk, Thomas Wagner, Yang Wang, Zhuoru Wang, Mark Wenig, Matthias Wiegner, Folkard Wittrock, Pinhua Xie, Chengzhi Xing, Jin Xu, Margarita Yela, Chengxin Zhang, and Xiaoyi Zhao
Atmos. Meas. Tech., 14, 1–35, https://doi.org/10.5194/amt-14-1-2021, https://doi.org/10.5194/amt-14-1-2021, 2021
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Multi-axis differential optical absorption spectroscopy (MAX-DOAS) is a ground-based remote sensing measurement technique that derives atmospheric aerosol and trace gas vertical profiles from skylight spectra. In this study, consistency and reliability of MAX-DOAS profiles are assessed by applying nine different evaluation algorithms to spectral data recorded during an intercomparison campaign in the Netherlands and by comparing the results to colocated supporting observations.
Zhuang Wang, Cheng Liu, Zhouqing Xie, Qihou Hu, Meinrat O. Andreae, Yunsheng Dong, Chun Zhao, Ting Liu, Yizhi Zhu, Haoran Liu, Chengzhi Xing, Wei Tan, Xiangguang Ji, Jinan Lin, and Jianguo Liu
Atmos. Chem. Phys., 20, 14917–14932, https://doi.org/10.5194/acp-20-14917-2020, https://doi.org/10.5194/acp-20-14917-2020, 2020
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Significant stratification of aerosols was observed in North China. Polluted dust dominated above the PBL, and anthropogenic aerosols prevailed within the PBL, which is mainly driven by meteorological conditions. The key role of the elevated dust is to alter atmospheric thermodynamics and stability, causing the suppression of turbulence exchange and a decrease in PBL height, especially during the dissipation stage, thereby inhibiting dissipation of persistent heavy surface haze pollution.
Wenjing Su, Cheng Liu, Ka Lok Chan, Qihou Hu, Haoran Liu, Xiangguang Ji, Yizhi Zhu, Ting Liu, Chengxin Zhang, Yujia Chen, and Jianguo Liu
Atmos. Meas. Tech., 13, 6271–6292, https://doi.org/10.5194/amt-13-6271-2020, https://doi.org/10.5194/amt-13-6271-2020, 2020
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The paper presents an improved retrieval of the TROPOMI tropospheric HCHO column over China. The new retrieval optimized both slant column retrieval and air mass factor calculation for TROPOMI observations of HCHO over China. The improved TROPOMI HCHO is subsequently validated by MAX-DOAS observations. Compared to the operational product, the improved HCHO agrees better with the MAX-DOAS data and thus is better suited for the analysis of regional- and city-scale pollution in China.
Yang Wang, Arnoud Apituley, Alkiviadis Bais, Steffen Beirle, Nuria Benavent, Alexander Borovski, Ilya Bruchkouski, Ka Lok Chan, Sebastian Donner, Theano Drosoglou, Henning Finkenzeller, Martina M. Friedrich, Udo Frieß, David Garcia-Nieto, Laura Gómez-Martín, François Hendrick, Andreas Hilboll, Junli Jin, Paul Johnston, Theodore K. Koenig, Karin Kreher, Vinod Kumar, Aleksandra Kyuberis, Johannes Lampel, Cheng Liu, Haoran Liu, Jianzhong Ma, Oleg L. Polyansky, Oleg Postylyakov, Richard Querel, Alfonso Saiz-Lopez, Stefan Schmitt, Xin Tian, Jan-Lukas Tirpitz, Michel Van Roozendael, Rainer Volkamer, Zhuoru Wang, Pinhua Xie, Chengzhi Xing, Jin Xu, Margarita Yela, Chengxin Zhang, and Thomas Wagner
Atmos. Meas. Tech., 13, 5087–5116, https://doi.org/10.5194/amt-13-5087-2020, https://doi.org/10.5194/amt-13-5087-2020, 2020
Youwen Sun, Cheng Liu, Lin Zhang, Mathias Palm, Justus Notholt, Hao Yin, Corinne Vigouroux, Erik Lutsch, Wei Wang, Changong Shan, Thomas Blumenstock, Tomoo Nagahama, Isamu Morino, Emmanuel Mahieu, Kimberly Strong, Bavo Langerock, Martine De Mazière, Qihou Hu, Huifang Zhang, Christof Petri, and Jianguo Liu
Atmos. Chem. Phys., 20, 5437–5456, https://doi.org/10.5194/acp-20-5437-2020, https://doi.org/10.5194/acp-20-5437-2020, 2020
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We present multiyear time series of ground-based Fourier-transform infrared spectroscopy measurements of HCN in densely populated eastern China. The seasonality and interannual variability of tropospheric HCN columns were investigated. The potential sources that drive the observed HCN seasonality and interannual variability were determined using a GEOS-Chem tagged CO simulation, global fire maps, and potential source contribution function values calculated using HYSPLIT back trajectories.
Karin Kreher, Michel Van Roozendael, Francois Hendrick, Arnoud Apituley, Ermioni Dimitropoulou, Udo Frieß, Andreas Richter, Thomas Wagner, Johannes Lampel, Nader Abuhassan, Li Ang, Monica Anguas, Alkis Bais, Nuria Benavent, Tim Bösch, Kristof Bognar, Alexander Borovski, Ilya Bruchkouski, Alexander Cede, Ka Lok Chan, Sebastian Donner, Theano Drosoglou, Caroline Fayt, Henning Finkenzeller, David Garcia-Nieto, Clio Gielen, Laura Gómez-Martín, Nan Hao, Bas Henzing, Jay R. Herman, Christian Hermans, Syedul Hoque, Hitoshi Irie, Junli Jin, Paul Johnston, Junaid Khayyam Butt, Fahim Khokhar, Theodore K. Koenig, Jonas Kuhn, Vinod Kumar, Cheng Liu, Jianzhong Ma, Alexis Merlaud, Abhishek K. Mishra, Moritz Müller, Monica Navarro-Comas, Mareike Ostendorf, Andrea Pazmino, Enno Peters, Gaia Pinardi, Manuel Pinharanda, Ankie Piters, Ulrich Platt, Oleg Postylyakov, Cristina Prados-Roman, Olga Puentedura, Richard Querel, Alfonso Saiz-Lopez, Anja Schönhardt, Stefan F. Schreier, André Seyler, Vinayak Sinha, Elena Spinei, Kimberly Strong, Frederik Tack, Xin Tian, Martin Tiefengraber, Jan-Lukas Tirpitz, Jeroen van Gent, Rainer Volkamer, Mihalis Vrekoussis, Shanshan Wang, Zhuoru Wang, Mark Wenig, Folkard Wittrock, Pinhua H. Xie, Jin Xu, Margarita Yela, Chengxin Zhang, and Xiaoyi Zhao
Atmos. Meas. Tech., 13, 2169–2208, https://doi.org/10.5194/amt-13-2169-2020, https://doi.org/10.5194/amt-13-2169-2020, 2020
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In September 2016, 36 spectrometers from 24 institutes measured a number of key atmospheric pollutants during an instrument intercomparison campaign (CINDI-2) at Cabauw, the Netherlands. Here we report on the outcome of this intercomparison exercise. The three major goals were to characterise the differences between the participating instruments, to define a robust methodology for performance assessment, and to contribute to the harmonisation of the measurement settings and retrieval methods.
Wei Wang, Cheng Liu, Lieven Clarisse, Martin Van Damme, Pierre-François Coheur, Yu Xie, Changgong Shan, Qihou Hu, Huifang Zhang, Youwen Sun, Hao Yin, and Nicholas Jones
Atmos. Meas. Tech. Discuss., https://doi.org/10.5194/amt-2020-39, https://doi.org/10.5194/amt-2020-39, 2020
Revised manuscript not accepted
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Ground-based FTIR observations are used to obtain the total columns and vertical profiles of atmospheric NH3 at a measurement site in Hefei, China. The spatial distribution, temporal variation, seasonal trend, and emission sources of NH3 are analyzed. FTIR observations captured the seasonal cycle of NH3. The IASI data are in broad agreement with our FTIR data. This is the first time that ground-based FTIR remote sensing of NH3 columns and comparison with satellite data are reported in China.
Meng Gao, Zirui Liu, Bo Zheng, Dongsheng Ji, Peter Sherman, Shaojie Song, Jinyuan Xin, Cheng Liu, Yuesi Wang, Qiang Zhang, Jia Xing, Jingkun Jiang, Zifa Wang, Gregory R. Carmichael, and Michael B. McElroy
Atmos. Chem. Phys., 20, 1497–1505, https://doi.org/10.5194/acp-20-1497-2020, https://doi.org/10.5194/acp-20-1497-2020, 2020
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We quantified the relative influences of anthropogenic emissions and meteorological conditions on PM2.5 concentrations in Beijing over the winters of 2002–2016. Meteorological conditions over the study period would have led to an increase of haze in Beijing, but the strict emission control measures have suppressed the unfavorable influences of the recent climate.
Jacob K. Hedelius, Tai-Long He, Dylan B. A. Jones, Bianca C. Baier, Rebecca R. Buchholz, Martine De Mazière, Nicholas M. Deutscher, Manvendra K. Dubey, Dietrich G. Feist, David W. T. Griffith, Frank Hase, Laura T. Iraci, Pascal Jeseck, Matthäus Kiel, Rigel Kivi, Cheng Liu, Isamu Morino, Justus Notholt, Young-Suk Oh, Hirofumi Ohyama, David F. Pollard, Markus Rettinger, Sébastien Roche, Coleen M. Roehl, Matthias Schneider, Kei Shiomi, Kimberly Strong, Ralf Sussmann, Colm Sweeney, Yao Té, Osamu Uchino, Voltaire A. Velazco, Wei Wang, Thorsten Warneke, Paul O. Wennberg, Helen M. Worden, and Debra Wunch
Atmos. Meas. Tech., 12, 5547–5572, https://doi.org/10.5194/amt-12-5547-2019, https://doi.org/10.5194/amt-12-5547-2019, 2019
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We seek ways to improve the accuracy of column measurements of carbon monoxide (CO) – an important tracer of pollution – made from the MOPITT satellite instrument. We devise a filtering scheme which reduces the scatter and also eliminates bias among the MOPITT detectors. Compared to ground-based observations, MOPITT measurements are about 6 %–8 % higher. When MOPITT data are implemented in a global assimilation model, they tend to reduce the model mismatch with aircraft measurements.
Mingchen Ma, Yang Gao, Yuhang Wang, Shaoqing Zhang, L. Ruby Leung, Cheng Liu, Shuxiao Wang, Bin Zhao, Xing Chang, Hang Su, Tianqi Zhang, Lifang Sheng, Xiaohong Yao, and Huiwang Gao
Atmos. Chem. Phys., 19, 12195–12207, https://doi.org/10.5194/acp-19-12195-2019, https://doi.org/10.5194/acp-19-12195-2019, 2019
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Ozone pollution has become severe in China, and extremely high ozone episodes occurred in summer 2017 over the North China Plain. While meteorology impacts are clear, we find that enhanced biogenic emissions, previously ignored by the community, driven by high vapor pressure deficit, land cover change and urban landscape contribute substantially to ozone formation. This study has significant implications for ozone pollution control with more frequent heat waves and urbanization growth in future.
Chengzhi Xing, Cheng Liu, Shanshan Wang, Qihou Hu, Haoran Liu, Wei Tan, Wenqiang Zhang, Bo Li, and Jianguo Liu
Atmos. Meas. Tech., 12, 3289–3302, https://doi.org/10.5194/amt-12-3289-2019, https://doi.org/10.5194/amt-12-3289-2019, 2019
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Ground-based MAX-DOAS has been utilized for the remote sensing of aerosol and trace gases for more than 10 years. Here we developed a new method to determine the aerosol optical properties, including scattering and absorption, from multiple-wavelength O4 absorptions from ground-based MAX-DOAS observations, which were validated well by other independent instruments at low elevations. It is beneficial to obtain the vertical profiles of aerosol properties using multiple elevations.
Wenjing Su, Cheng Liu, Qihou Hu, Shaohua Zhao, Youwen Sun, Wei Wang, Yizhi Zhu, Jianguo Liu, and Jhoon Kim
Atmos. Chem. Phys., 19, 6717–6736, https://doi.org/10.5194/acp-19-6717-2019, https://doi.org/10.5194/acp-19-6717-2019, 2019
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For a better understanding of HCHO pollution and atmospheric chemistry, we evaluated primary and secondary sources of HCHO in the Yangtze River Delta based on HCHO column density from OMPS and combined this with in situ surface measurements. We found that secondary formation contributed most to ambient HCHO over longer timescales, but primary emission could be dominant in the winter. Hence, the usability of total HCHO as a proxy of VOC reactivity depends on the timescale of interest.
Jingyuan Shao, Qianjie Chen, Yuxuan Wang, Xiao Lu, Pengzhen He, Yele Sun, Viral Shah, Randall V. Martin, Sajeev Philip, Shaojie Song, Yue Zhao, Zhouqing Xie, Lin Zhang, and Becky Alexander
Atmos. Chem. Phys., 19, 6107–6123, https://doi.org/10.5194/acp-19-6107-2019, https://doi.org/10.5194/acp-19-6107-2019, 2019
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Sulfate is a key species contributing to particle formation and growth during wintertime Chinese haze events. This study combines observations and modeling of oxygen isotope signatures in sulfate aerosol to investigate its formation mechanisms, with a focus on heterogeneous production on aerosol surface via H2O2, O3, and NO2 and trace metal catalyzed oxidation. Contributions from different formation pathways are presented.
Xiaofei Qin, Xiaohao Wang, Yijie Shi, Guangyuan Yu, Na Zhao, Yanfen Lin, Qingyan Fu, Dongfang Wang, Zhouqing Xie, Congrui Deng, and Kan Huang
Atmos. Chem. Phys., 19, 5923–5940, https://doi.org/10.5194/acp-19-5923-2019, https://doi.org/10.5194/acp-19-5923-2019, 2019
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The seasonal pattern of atmospheric mercury species over a regional transport intersection zone in east China indicated impacts from both natural re-emissions and anthropogenic emissions. Quasi-local sources were more important than long-range transport for mercury, opposite from particles. Shipping activities were especially outstanding emissions. Abnormally high GOM was ascribed to the high oxidant levels. The gas–particle partition inhibited the formation of GOM under high particle levels.
Yuqing Ye, Zhouqing Xie, Ming Zhu, and Xinming Wang
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2019-410, https://doi.org/10.5194/acp-2019-410, 2019
Preprint withdrawn
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Aerosol samples from the Arctic Ocean and Antarctic atmosphere were analysed by ultrahigh resolution mass spectrometry coupled with negative ion mode electrospray ionization. Hundreds of organic compounds, including organosulfates, nitrooxy-organosulfates, organonitrates and oxygenated hydrocarbons, were detected. Our study presents the first overview of OSs and ONs in the polar regions and promotes the understanding of their characteristics and sources.
Xin Tian, Pinhua Xie, Jin Xu, Yang Wang, Ang Li, Fengcheng Wu, Zhaokun Hu, Cheng Liu, and Qiong Zhang
Atmos. Chem. Phys., 19, 3375–3393, https://doi.org/10.5194/acp-19-3375-2019, https://doi.org/10.5194/acp-19-3375-2019, 2019
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We used the MAX-DOAS instrument installed at the UCAS, Beijing, to evaluate effects on HCHO. The daily variation, transport, sources, and the effect of APEC emission control measures on HCHO were analyzed. Dependences of HCHO VCDs on wind fields indicated that the HCHO values were affected by the transport of pollutants from the south. The results from comparing the MAX-DOAS with the CAMS model indicate the CAMS model can simulate the effects of transport and the secondary sources of HCHO well.
Junting Zhong, Xiaoye Zhang, Yaqiang Wang, Jizhi Wang, Xiaojing Shen, Hongsheng Zhang, Tijian Wang, Zhouqing Xie, Cheng Liu, Hengde Zhang, Tianliang Zhao, Junying Sun, Shaojia Fan, Zhiqiu Gao, Yubin Li, and Linlin Wang
Atmos. Chem. Phys., 19, 3287–3306, https://doi.org/10.5194/acp-19-3287-2019, https://doi.org/10.5194/acp-19-3287-2019, 2019
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In various haze regions in China, including the Guanzhong Plain, the middle and lower reaches of the Yangtze River, the Pearl River Delta, the Sichuan Basin, and the Northeast China Plain, heavy aerosol pollution episodes include inter-/trans-regional transport stages and cumulative stages (CSs). During CSs a two-way feedback mechanism exists between unfavorable meteorological conditions and cumulative aerosol pollution. This two-way feedback is further quantified and its magnitude is compared.
Chang-Gong Shan, Wei Wang, Cheng Liu, You-Wen Sun, Yuan Tian, and Isamu Morino
Geosci. Instrum. Method. Data Syst. Discuss., https://doi.org/10.5194/gi-2018-43, https://doi.org/10.5194/gi-2018-43, 2018
Publication in GI not foreseen
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Observations of the stable isotopes of water vapor by high-resolution ground-based Fourier transform infrared spectroscopy (FTIR) provide information on study of the variation of the atmospheric water vapor at Hefei site. In this paper, the percentage of atmospheric H2O(XH2O) and HDO (XHDO) have been retrieved based on a high-resolution ground-based FTIR at Hefei site, and also calculated the stable isotopes of water composition δD. The time series of XH2O were compared with the Greenhouse gase.
Wei Tan, Cheng Liu, Shanshan Wang, Chengzhi Xing, Wenjing Su, Chengxin Zhang, Congzi Xia, Haoran Liu, Zhaonan Cai, and Jianguo Liu
Atmos. Chem. Phys., 18, 15387–15402, https://doi.org/10.5194/acp-18-15387-2018, https://doi.org/10.5194/acp-18-15387-2018, 2018
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This ship-based observation in June 2017 has, for the first time, reported the vertical column densities of NO2, SO2, and HCHO over oceanic areas of the East China Sea, which show good agreement with satellite observations. High levels of trace gases over oceanic areas were identified to be related to the regional transport of air pollutants from continental areas and nearby ship emissions.
Youwen Sun, Cheng Liu, Mathias Palm, Corinne Vigouroux, Justus Notholt, Qihou Hu, Nicholas Jones, Wei Wang, Wenjing Su, Wenqiang Zhang, Changong Shan, Yuan Tian, Xingwei Xu, Martine De Mazière, Minqiang Zhou, and Jianguo Liu
Atmos. Chem. Phys., 18, 14569–14583, https://doi.org/10.5194/acp-18-14569-2018, https://doi.org/10.5194/acp-18-14569-2018, 2018
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The seasonal evolution of O3 and its photochemical production regime in a polluted region of eastern China between 2014 and 2017 was investigated using FTS observations. We observed a broad summer O3 maximum in Hefei, China, and the ozone production is mainly NOx limited in spring and summer and is mainly VOC or mixed VOC–NOx limited in autumn and winter.
Youwen Sun, Mathias Palm, Cheng Liu, Frank Hase, David Griffith, Christine Weinzierl, Christof Petri, Wei Wang, and Justus Notholt
Atmos. Meas. Tech., 11, 2879–2896, https://doi.org/10.5194/amt-11-2879-2018, https://doi.org/10.5194/amt-11-2879-2018, 2018
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We simulated instrumental line shape (ILS) degradations with respect to typical types of misalignment, and compared their influence on each NDACC gas. The requirements to suppress the ILS-degradation-related biases within a specified accuracy for all NDACC gases were deduced.
Qianqian Hong, Cheng Liu, Ka Lok Chan, Qihou Hu, Zhouqing Xie, Haoran Liu, Fuqi Si, and Jianguo Liu
Atmos. Chem. Phys., 18, 5931–5951, https://doi.org/10.5194/acp-18-5931-2018, https://doi.org/10.5194/acp-18-5931-2018, 2018
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We presented ship-based MAX-DOAS measurements of tropospheric trace gases' distribution along the eastern part of the Yangtze River during winter 2015. Tropospheric VCDs of NO2, SO2, and HCHO were retrieved from MAX-DOAS measurement spectra. Enhanced tropospheric NO2 and SO2 VCDs were detected over downwind areas of industrial zones over the Yangtze River. Our results indicate that different pollution control strategies should be applied in different provinces.
Pengzhen He, Becky Alexander, Lei Geng, Xiyuan Chi, Shidong Fan, Haicong Zhan, Hui Kang, Guangjie Zheng, Yafang Cheng, Hang Su, Cheng Liu, and Zhouqing Xie
Atmos. Chem. Phys., 18, 5515–5528, https://doi.org/10.5194/acp-18-5515-2018, https://doi.org/10.5194/acp-18-5515-2018, 2018
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We use observations of the oxygen isotopic composition of sulfate aerosol as a fingerprint to quantify various sulfate formation mechanisms during pollution events in Beijing, China. We found that heterogeneous reactions on aerosols dominated sulfate production in general; however, in-cloud reactions would dominate haze sulfate production when cloud liquid water content was high. The findings also suggest the heterogeneity of aerosol acidity should be parameterized in models.
Junting Zhong, Xiaoye Zhang, Yunsheng Dong, Yaqiang Wang, Cheng Liu, Jizhi Wang, Yangmei Zhang, and Haochi Che
Atmos. Chem. Phys., 18, 247–258, https://doi.org/10.5194/acp-18-247-2018, https://doi.org/10.5194/acp-18-247-2018, 2018
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Beijing heavy pollution episodes are characterized by the transport stage (TS) and the cumulative stage (CS). PM2.5 pollution formation in the TS is primarily caused by pollutants transported from the south of Beijing. PM2.5 cumulative explosive growth in the CS is dominated by stable atmospheric stratification due to the interaction of particulate matter (PM) and meteorological factors. The positive meteorological feedback on PM2.5 mass noted explains over 70% of cumulative explosive growth.
Chengzhi Xing, Cheng Liu, Shanshan Wang, Ka Lok Chan, Yang Gao, Xin Huang, Wenjing Su, Chengxin Zhang, Yunsheng Dong, Guangqiang Fan, Tianshu Zhang, Zhenyi Chen, Qihou Hu, Hang Su, Zhouqing Xie, and Jianguo Liu
Atmos. Chem. Phys., 17, 14275–14289, https://doi.org/10.5194/acp-17-14275-2017, https://doi.org/10.5194/acp-17-14275-2017, 2017
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Vertical profiles of the aerosol extinction coefficient and NO2 and HCHO concentrations were retrieved from MAX-DOAS measurement, while vertical distribution of O3 was obtained using ozone lidar. The measured O3 vertical distribution indicates that the ozone production not only occurs at surface level but also at higher altitudes (about 1.1 km), which are not directly related to horizontal and vertical transportation but are mainly influenced by the abundance of VOCs in the lower troposphere.
Wei Wang, Yuan Tian, Cheng Liu, Youwen Sun, Wenqing Liu, Pinhua Xie, Jianguo Liu, Jin Xu, Isamu Morino, Voltaire A. Velazco, David W. T. Griffith, Justus Notholt, and Thorsten Warneke
Atmos. Meas. Tech., 10, 2627–2643, https://doi.org/10.5194/amt-10-2627-2017, https://doi.org/10.5194/amt-10-2627-2017, 2017
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A ground-based high-resolution Fourier transform spectrometer (FTS) station has been established in Hefei, China to remotely measure CO2, CO and other greenhouse gases. Our research aim is to provide information for constraining regional sources and sinks, and validate satellite data, such as GOSAT, OCO-2 and TANSAT. We investigate the potential of FTS to determine the temporal variability of atmospheric CO2 and CO, and assess the ability of our observations to validate satellite data.
Yang Wang, Steffen Beirle, Johannes Lampel, Mariliza Koukouli, Isabelle De Smedt, Nicolas Theys, Ang Li, Dexia Wu, Pinhua Xie, Cheng Liu, Michel Van Roozendael, Trissevgeni Stavrakou, Jean-François Müller, and Thomas Wagner
Atmos. Chem. Phys., 17, 5007–5033, https://doi.org/10.5194/acp-17-5007-2017, https://doi.org/10.5194/acp-17-5007-2017, 2017
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A long-term MAX-DOAS measurement from 2011 to 2014 was operated in Wuxi, part of the most industrialized area of the Yangtze River delta region of China. The tropospheric VCDs and vertical profiles of NO2, SO2 and HCHO derived from the MAX-DOAS are used to validate the products derived from OMI and GOME-2A/B by different scientific teams (daily- and bimonthly-averaged data). We investigate the effects of clouds, aerosols and a priori profile shapes on satellite retrievals of tropospheric VCDs.
Youwen Sun, Mathias Palm, Christine Weinzierl, Christof Petri, Justus Notholt, Yuting Wang, and Cheng Liu
Atmos. Meas. Tech., 10, 989–997, https://doi.org/10.5194/amt-10-989-2017, https://doi.org/10.5194/amt-10-989-2017, 2017
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We first design experiments to investigate the sensitivity of ILS (instrumental line shape) monitoring for a high-resolution FTIR spectrometer within the TCCON and NDACC networks with respect to different optical attenuators. The ILS characteristics derived from lamp and sun spectra are in good agreement. A potential strategy to adapt incident intensity of a detector was deduced.
Enno Peters, Gaia Pinardi, André Seyler, Andreas Richter, Folkard Wittrock, Tim Bösch, Michel Van Roozendael, François Hendrick, Theano Drosoglou, Alkiviadis F. Bais, Yugo Kanaya, Xiaoyi Zhao, Kimberly Strong, Johannes Lampel, Rainer Volkamer, Theodore Koenig, Ivan Ortega, Olga Puentedura, Mónica Navarro-Comas, Laura Gómez, Margarita Yela González, Ankie Piters, Julia Remmers, Yang Wang, Thomas Wagner, Shanshan Wang, Alfonso Saiz-Lopez, David García-Nieto, Carlos A. Cuevas, Nuria Benavent, Richard Querel, Paul Johnston, Oleg Postylyakov, Alexander Borovski, Alexander Elokhov, Ilya Bruchkouski, Haoran Liu, Cheng Liu, Qianqian Hong, Claudia Rivera, Michel Grutter, Wolfgang Stremme, M. Fahim Khokhar, Junaid Khayyam, and John P. Burrows
Atmos. Meas. Tech., 10, 955–978, https://doi.org/10.5194/amt-10-955-2017, https://doi.org/10.5194/amt-10-955-2017, 2017
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This work is about harmonization of differential optical absorption spectroscopy retrieval codes, which is a remote sensing technique widely used to derive atmospheric trace gas amounts. The study is based on ground-based measurements performed during the Multi-Axis DOAS Comparison campaign for Aerosols and Trace gases (MAD-CAT) in Mainz, Germany, in summer 2013. In total, 17 international groups working in the field of the DOAS technique participated in this study.
Qianqian Hong, Zhouqing Xie, Cheng Liu, Feiyue Wang, Pinhua Xie, Hui Kang, Jin Xu, Jiancheng Wang, Fengcheng Wu, Pengzhen He, Fusheng Mou, Shidong Fan, Yunsheng Dong, Haicong Zhan, Xiawei Yu, Xiyuan Chi, and Jianguo Liu
Atmos. Chem. Phys., 16, 13807–13821, https://doi.org/10.5194/acp-16-13807-2016, https://doi.org/10.5194/acp-16-13807-2016, 2016
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It is known that rapid industrialization in developing countries has led to an increase in air pollution. Here we firstly report the speciated atmospheric mercury during haze days based upon 1-year synchronous observations in an inland city in China. The findings provide direct evidence to understand the biogeochemical cycles of atmospheric mercury related to air pollution and an opportunity to evaluate the potential health risks of atmospheric mercury.
Qianjie Chen, Lei Geng, Johan A. Schmidt, Zhouqing Xie, Hui Kang, Jordi Dachs, Jihong Cole-Dai, Andrew J. Schauer, Madeline G. Camp, and Becky Alexander
Atmos. Chem. Phys., 16, 11433–11450, https://doi.org/10.5194/acp-16-11433-2016, https://doi.org/10.5194/acp-16-11433-2016, 2016
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The formation mechanisms of sulfate in the marine boundary layer are not well understood, which could result in large uncertainties in aerosol radiative forcing. We measure the oxygen isotopic composition (Δ17O) of sulfate collected in the MBL and analyze with a global transport model. Our results suggest that 33–50 % of MBL sulfate is formed via oxidation of S(IV) by hypohalous acids HOBr / HOCl in the aqueous phase, and the daily-mean HOBr/HOCl concentrations are on the order of 0.01–0.1 ppt.
Xiawei Yu, Zhibin Wang, Minghui Zhang, Uwe Kuhn, Zhouqing Xie, Yafang Cheng, Ulrich Pöschl, and Hang Su
Atmos. Chem. Phys., 16, 11337–11348, https://doi.org/10.5194/acp-16-11337-2016, https://doi.org/10.5194/acp-16-11337-2016, 2016
Youwen Sun, Cheng Liu, Pinhua Xie, Andreas Hartl, Kalok Chan, Yuan Tian, Wei Wang, Min Qin, Jianguo Liu, and Wenqing Liu
Atmos. Meas. Tech., 9, 1167–1180, https://doi.org/10.5194/amt-9-1167-2016, https://doi.org/10.5194/amt-9-1167-2016, 2016
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SO2 variability over a large concentration range and interferences from other gases have been major limitations in industrial SO2 emission monitoring. This study demonstrates accurate industrial SO2 emission monitoring through a portable multichannel gas analyzer with an optimized retrieval algorithm. The developed instrument shows good performance in both the linear and nonlinear ranges.
Related subject area
Subject: Isotopes | Research Activity: Laboratory Studies | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
On the potential fingerprint of the Antarctic ozone hole in ice-core nitrate isotopes: a case study based on a South Pole ice core
Quantifying the nitrogen isotope effects during photochemical equilibrium between NO and NO2: implications for δ15N in tropospheric reactive nitrogen
Temporal variation in 129I and 127I in aerosols from Xi'an, China: influence of East Asian monsoon and heavy haze events
High time-resolved measurement of stable carbon isotope composition in water-soluble organic aerosols: method optimization and a case study during winter haze in eastern China
Dependence between the photochemical age of light aromatic hydrocarbons and the carbon isotope ratios of atmospheric nitrophenols
Evidence for a major missing source in the global chloromethane budget from stable carbon isotopes
Mass spectrometric measurement of hydrogen isotope fractionation for the reactions of chloromethane with OH and Cl
Stable carbon isotope ratios of ambient aromatic volatile organic compounds
Kinetic isotope effects of 12CH3D + OH and 13CH3D + OH from 278 to 313 K
Investigation of post-depositional processing of nitrate in East Antarctic snow: isotopic constraints on photolytic loss, re-oxidation, and source inputs
Chlorine isotope composition in chlorofluorocarbons CFC-11, CFC-12 and CFC-113 in firn, stratospheric and tropospheric air
NOx cycle and the tropospheric ozone isotope anomaly: an experimental investigation
Fractionation of sulfur isotopes during heterogeneous oxidation of SO2 on sea salt aerosol: a new tool to investigate non-sea salt sulfate production in the marine boundary layer
Sulfur isotope fractionation during oxidation of sulfur dioxide: gas-phase oxidation by OH radicals and aqueous oxidation by H2O2, O3 and iron catalysis
Molecular hydrogen (H2) emissions and their isotopic signatures (H/D) from a motor vehicle: implications on atmospheric H2
Isotope effect in the formation of H2 from H2CO studied at the atmospheric simulation chamber SAPHIR
Pressure dependence of the deuterium isotope effect in the photolysis of formaldehyde by ultraviolet light
Yanzhi Cao, Zhuang Jiang, Becky Alexander, Jihong Cole-Dai, Joel Savarino, Joseph Erbland, and Lei Geng
Atmos. Chem. Phys., 22, 13407–13422, https://doi.org/10.5194/acp-22-13407-2022, https://doi.org/10.5194/acp-22-13407-2022, 2022
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We investigate the potential of ice-core preserved nitrate isotopes as proxies of stratospheric ozone variability by measuring nitrate isotopes in a shallow ice core from the South Pole. The large variability in the snow accumulation rate and its slight increase after the 1970s masked any signals caused by the ozone hole. Moreover, the nitrate oxygen isotope decrease may reflect changes in the atmospheric oxidation environment in the Southern Ocean.
Jianghanyang Li, Xuan Zhang, John Orlando, Geoffrey Tyndall, and Greg Michalski
Atmos. Chem. Phys., 20, 9805–9819, https://doi.org/10.5194/acp-20-9805-2020, https://doi.org/10.5194/acp-20-9805-2020, 2020
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Nitrogen isotopic compositions of atmospheric reactive nitrogen are widely used to infer their sources. However, the reactions between NO and NO2 strongly impact their isotopes, which was not well understood. We conducted a series of experiments in an atmospheric simulation chamber to determine the isotopic effects of (1) direct isotopic exchange between NO and NO2 and (2) the isotopic fractionations during NOx photochemistry, then developed an equation to quantify the overall isotopic effect.
Luyuan Zhang, Xiaolin Hou, Sheng Xu, Tian Feng, Peng Cheng, Yunchong Fu, and Ning Chen
Atmos. Chem. Phys., 20, 2623–2635, https://doi.org/10.5194/acp-20-2623-2020, https://doi.org/10.5194/acp-20-2623-2020, 2020
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To trace the long-range transport of air pollutants and understand the atmospheric effect of iodine, the daily-resolution temporal variations of 129I and 127I in aerosols from a monsoonal city indicate the East Asian monsoon and fossil fuel combustion plays crucial roles on transport of 129I from Europe to East Asia and on elevated 127I concentrations. Through linking iodine isotopes with five major air pollutants, this study proposes the possible role of iodine in urban air pollution.
Wenqi Zhang, Yan-Lin Zhang, Fang Cao, Yankun Xiang, Yuanyuan Zhang, Mengying Bao, Xiaoyan Liu, and Yu-Chi Lin
Atmos. Chem. Phys., 19, 11071–11087, https://doi.org/10.5194/acp-19-11071-2019, https://doi.org/10.5194/acp-19-11071-2019, 2019
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A novel method to determine the concentration and the isotopes of WSOC in aerosols is established and applied in the analysis of a severe haze in eastern China. The results show that the studied site is affected by the photochemical aging, biomass burning and dust aerosols in different episodes during the sampling period. The analysis of WSOC and its isotopes offers a great potential to better understand the source emission, the atmospheric aging and the secondary production of WSOC.
Marina Saccon, Anna Kornilova, Lin Huang, and Jochen Rudolph
Atmos. Chem. Phys., 19, 5495–5509, https://doi.org/10.5194/acp-19-5495-2019, https://doi.org/10.5194/acp-19-5495-2019, 2019
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As compound are emitted into the atmosphere, they can undergo chemical reactions to produce secondary products. This paper investigates the relations of compounds' unique chemical characteristics to the processes that formed them from emissions in the atmosphere. A model is applied to help with this investigation. The complexity of the atmosphere, including mixing of air masses and variability in precursor reactivity, is taken into consideration, and results are presented.
Enno Bahlmann, Frank Keppler, Julian Wittmer, Markus Greule, Heinz Friedrich Schöler, Richard Seifert, and Cornelius Zetzsch
Atmos. Chem. Phys., 19, 1703–1719, https://doi.org/10.5194/acp-19-1703-2019, https://doi.org/10.5194/acp-19-1703-2019, 2019
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Chloromethane is the most important natural carrier of chlorine to the stratosphere. From a newly determined carbon isotope effect of −11.2 ‰ for the tropospheric loss of CH3Cl we derive a tropical rainforest CH3Cl source of 670 ± 200 Gg a−1, 60 % smaller than previous estimates. A revision of previous bottom-up estimates using above-ground biomass instead of rainforest area strongly supports this lower estimate. Our results suggest a large unknown tropical value of 1530 ± 200 Gg a−1.
Frank Keppler, Enno Bahlmann, Markus Greule, Heinz Friedrich Schöler, Julian Wittmer, and Cornelius Zetzsch
Atmos. Chem. Phys., 18, 6625–6635, https://doi.org/10.5194/acp-18-6625-2018, https://doi.org/10.5194/acp-18-6625-2018, 2018
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Chloromethane is involved in stratospheric ozone depletion, but detailed knowledge of its global budget is missing. In this study stable hydrogen isotope analyses were performed to investigate the dominant loss process for atmospheric chloromethane with photochemically produced hydroxyl radicals. The findings might have significant implications for the use of stable isotope signatures in elucidation of global chloromethane cycling.
Anna Kornilova, Lin Huang, Marina Saccon, and Jochen Rudolph
Atmos. Chem. Phys., 16, 11755–11772, https://doi.org/10.5194/acp-16-11755-2016, https://doi.org/10.5194/acp-16-11755-2016, 2016
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The photochemical oxidation of organic compounds in the atmosphere results in the formation of important secondary pollutants such as ozone and fine particles. The extent of oxidation the organic compounds have been subjected too since there emissions is essential is key for understanding the formation of secondary pollutants. This paper demonstrates that measurements of the carbon isotope ratios allow determining the extent of photochemical processing for individual compounds.
L. M. T. Joelsson, J. A. Schmidt, E. J. K. Nilsson, T. Blunier, D. W. T. Griffith, S. Ono, and M. S. Johnson
Atmos. Chem. Phys., 16, 4439–4449, https://doi.org/10.5194/acp-16-4439-2016, https://doi.org/10.5194/acp-16-4439-2016, 2016
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We present experimental kinetic isotope effects (KIE) for the OH oxidation of CH3D and 13CH3D and their temperature dependence. Our determination of the 13CH3D + OH KIE is novel and we find no "clumped" isotope effect within the experimental uncertainty.
G. Shi, A. M. Buffen, M. G. Hastings, C. Li, H. Ma, Y. Li, B. Sun, C. An, and S. Jiang
Atmos. Chem. Phys., 15, 9435–9453, https://doi.org/10.5194/acp-15-9435-2015, https://doi.org/10.5194/acp-15-9435-2015, 2015
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We evaluate isotopic composition of NO3- in different environments across East Antarctica. At high snow accumulation sites, isotopic ratios are suggestive of preservation of NO3- deposition. At low accumulation sites, isotopes are sensitive to both the loss of NO3- due to photolysis and secondary formation of NO3- within the snow. The imprint of post-depositional alteration is not uniform with depth, making it difficult to predict the isotopic composition at depth from near-surface data alone.
S. J. Allin, J. C. Laube, E. Witrant, J. Kaiser, E. McKenna, P. Dennis, R. Mulvaney, E. Capron, P. Martinerie, T. Röckmann, T. Blunier, J. Schwander, P. J. Fraser, R. L. Langenfelds, and W. T. Sturges
Atmos. Chem. Phys., 15, 6867–6877, https://doi.org/10.5194/acp-15-6867-2015, https://doi.org/10.5194/acp-15-6867-2015, 2015
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Stratospheric ozone protects life on Earth from harmful UV-B radiation. Chlorofluorocarbons (CFCs) are man-made compounds which act to destroy this barrier.
This paper presents (1) the first measurements of the stratospheric δ(37Cl) of CFCs -11 and -113; (2) the first quantification of long-term trends in the tropospheric δ(37Cl) of CFCs -11, -12 and -113.
This study provides a better understanding of source and sink processes associated with these destructive compounds.
G. Michalski, S. K. Bhattacharya, and G. Girsch
Atmos. Chem. Phys., 14, 4935–4953, https://doi.org/10.5194/acp-14-4935-2014, https://doi.org/10.5194/acp-14-4935-2014, 2014
E. Harris, B. Sinha, P. Hoppe, S. Foley, and S. Borrmann
Atmos. Chem. Phys., 12, 4619–4631, https://doi.org/10.5194/acp-12-4619-2012, https://doi.org/10.5194/acp-12-4619-2012, 2012
E. Harris, B. Sinha, P. Hoppe, J. N. Crowley, S. Ono, and S. Foley
Atmos. Chem. Phys., 12, 407–423, https://doi.org/10.5194/acp-12-407-2012, https://doi.org/10.5194/acp-12-407-2012, 2012
M. K. Vollmer, S. Walter, S. W. Bond, P. Soltic, and T. Röckmann
Atmos. Chem. Phys., 10, 5707–5718, https://doi.org/10.5194/acp-10-5707-2010, https://doi.org/10.5194/acp-10-5707-2010, 2010
T. Röckmann, S. Walter, B. Bohn, R. Wegener, H. Spahn, T. Brauers, R. Tillmann, E. Schlosser, R. Koppmann, and F. Rohrer
Atmos. Chem. Phys., 10, 5343–5357, https://doi.org/10.5194/acp-10-5343-2010, https://doi.org/10.5194/acp-10-5343-2010, 2010
E. J. K. Nilsson, V. F. Andersen, H. Skov, and M. S. Johnson
Atmos. Chem. Phys., 10, 3455–3462, https://doi.org/10.5194/acp-10-3455-2010, https://doi.org/10.5194/acp-10-3455-2010, 2010
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Short summary
We present the first observations of the oxygen-17 excess of atmospheric nitrate (Δ17O(NO−3)) collected in Beijing haze to reveal the relative importance of different nitrate formation pathways. We found that nocturnal pathways (N2O5 + H2O/Cl– and NO3 + HC) dominated nitrate production during polluted days (PM2.5 ≥ 75 μg m–3), with a mean possible fraction of 56–97 %.
We present the first observations of the oxygen-17 excess of atmospheric nitrate (Δ17O(NO−3))...
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