Articles | Volume 12, issue 24
https://doi.org/10.5194/acp-12-12103-2012
© Author(s) 2012. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
https://doi.org/10.5194/acp-12-12103-2012
© Author(s) 2012. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Research article
| 
20 Dec 2012
Research article |
| 20 Dec 2012
Characteristics of atmospheric Total Gaseous Mercury (TGM) observed in urban Nanjing, China
School of Atmospheric Sciences, Nanjing University, Nanjing 210093, China
T. Wang
School of Atmospheric Sciences, Nanjing University, Nanjing 210093, China
R. Talbot
Department of Earth & Atmospheric Sciences, University of Houston, Houston, TX 77204, USA
H. Mao
Department of Chemistry, State University of New York, College of Environmental Science and Forestry, Syracuse, NY 13219, USA
C. B. Hall
Department of Chemistry, State University of New York, College of Environmental Science and Forestry, Syracuse, NY 13219, USA
X. Yang
School of Atmospheric Sciences, Nanjing University, Nanjing 210093, China
C. Fu
School of Atmospheric Sciences, Nanjing University, Nanjing 210093, China
B. Zhuang
School of Atmospheric Sciences, Nanjing University, Nanjing 210093, China
S. Li
School of Atmospheric Sciences, Nanjing University, Nanjing 210093, China
Y. Han
School of Atmospheric Sciences, Nanjing University, Nanjing 210093, China
X. Huang
School of Atmospheric Sciences, Nanjing University, Nanjing 210093, China
Related authors
Huisheng Bian, Mian Chin, Peter R. Colarco, Eric C. Apel, Donald R. Blake, Karl Froyd, Rebecca S. Hornbrook, Jose Jimenez, Pedro Campuzano Jost, Michael Lawler, Mingxu Liu, Marianne Tronstad Lund, Hitoshi Matsui, Benjamin A. Nault, Joyce E. Penner, Andrew W. Rollins, Gregory Schill, Ragnhild B. Skeie, Hailong Wang, Lu Xu, Kai Zhang, and Jialei Zhu
Atmos. Chem. Phys., 24, 1717–1741, https://doi.org/10.5194/acp-24-1717-2024, https://doi.org/10.5194/acp-24-1717-2024, 2024
Short summary
Short summary
This work studies sulfur in the remote troposphere at global and seasonal scales using aircraft measurements and multi-model simulations. The goal is to understand the sulfur cycle over remote oceans, spread of model simulations, and observation–model discrepancies. Such an understanding and comparison with real observations are crucial to narrow down the uncertainties in model sulfur simulations and improve understanding of the sulfur cycle in atmospheric air quality, climate, and ecosystems.
Lehui Cui, Yunting Xiao, Wei Hu, Lei Song, Yujue Wang, Chao Zhang, Pingqing Fu, and Jialei Zhu
Earth Syst. Sci. Data, 15, 5403–5425, https://doi.org/10.5194/essd-15-5403-2023, https://doi.org/10.5194/essd-15-5403-2023, 2023
Short summary
Short summary
Isoprene is a crucial non-methane biogenic volatile organic compound with the largest global emissions, which has high chemical reactivity and serves as the primary source of natural secondary organic aerosols. This study built a module to present a 20-year global hourly dataset of marine phytoplankton-generated biological and photochemistry-generated isoprene emissions in the sea microlayers based on the latest advancements in biological, physical, and chemical processes.
Shujun Zhong, Shuang Chen, Junjun Deng, Yanbing Fan, Qiang Zhang, Qiaorong Xie, Yulin Qi, Wei Hu, Libin Wu, Xiaodong Li, Chandra Mouli Pavuluri, Jialei Zhu, Xin Wang, Di Liu, Xiaole Pan, Yele Sun, Zifa Wang, Yisheng Xu, Haijie Tong, Hang Su, Yafang Cheng, Kimitaka Kawamura, and Pingqing Fu
Atmos. Chem. Phys., 23, 2061–2077, https://doi.org/10.5194/acp-23-2061-2023, https://doi.org/10.5194/acp-23-2061-2023, 2023
Short summary
Short summary
This study investigated the role of the secondary organic aerosol (SOA) loading on the molecular composition of wintertime urban aerosols by ultrahigh-resolution mass spectrometry. Results demonstrate that the SOA loading is an important factor associated with the oxidation degree, nitrate group content, and chemodiversity of nitrooxy–organosulfates. Our study also found that the hydrolysis of nitrooxy–organosulfates is a possible pathway for the formation of organosulfates.
Qirui Zhong, Nick Schutgens, Guido van der Werf, Twan van Noije, Kostas Tsigaridis, Susanne E. Bauer, Tero Mielonen, Alf Kirkevåg, Øyvind Seland, Harri Kokkola, Ramiro Checa-Garcia, David Neubauer, Zak Kipling, Hitoshi Matsui, Paul Ginoux, Toshihiko Takemura, Philippe Le Sager, Samuel Rémy, Huisheng Bian, Mian Chin, Kai Zhang, Jialei Zhu, Svetlana G. Tsyro, Gabriele Curci, Anna Protonotariou, Ben Johnson, Joyce E. Penner, Nicolas Bellouin, Ragnhild B. Skeie, and Gunnar Myhre
Atmos. Chem. Phys., 22, 11009–11032, https://doi.org/10.5194/acp-22-11009-2022, https://doi.org/10.5194/acp-22-11009-2022, 2022
Short summary
Short summary
Aerosol optical depth (AOD) errors for biomass burning aerosol (BBA) are evaluated in 18 global models against satellite datasets. Notwithstanding biases in satellite products, they allow model evaluations. We observe large and diverse model biases due to errors in BBA. Further interpretations of AOD diversities suggest large biases exist in key processes for BBA which require better constraining. These results can contribute to further model improvement and development.
Junjun Deng, Hao Ma, Xinfeng Wang, Shujun Zhong, Zhimin Zhang, Jialei Zhu, Yanbing Fan, Wei Hu, Libin Wu, Xiaodong Li, Lujie Ren, Chandra Mouli Pavuluri, Xiaole Pan, Yele Sun, Zifa Wang, Kimitaka Kawamura, and Pingqing Fu
Atmos. Chem. Phys., 22, 6449–6470, https://doi.org/10.5194/acp-22-6449-2022, https://doi.org/10.5194/acp-22-6449-2022, 2022
Short summary
Short summary
Light-absorbing brown carbon (BrC) plays an important role in climate change and atmospheric chemistry. Here we investigated the seasonal and diurnal variations in water-soluble BrC in PM2.5 in the megacity Tianjin in coastal China. Results of the source apportionments from the combination with organic molecular compositions and optical properties of water-soluble BrC reveal a large contribution from primary bioaerosol particles to BrC in the urban atmosphere.
Junjun Deng, Hao Guo, Hongliang Zhang, Jialei Zhu, Xin Wang, and Pingqing Fu
Atmos. Chem. Phys., 20, 14419–14435, https://doi.org/10.5194/acp-20-14419-2020, https://doi.org/10.5194/acp-20-14419-2020, 2020
Short summary
Short summary
One-year source apportionment of BC aerosols in a coastal city in China was conducted with the light-absorption observation-based method and source-oriented model. Source contributions identified by the two source apportionment methods were compared. Temporal variability, potential sources and transport pathways of BC from fossil fuel and biomass burning were characterized. Significant influence of biomass burning in North and East–Central China on BC in the region was highlighted.
Jialei Zhu and Joyce E. Penner
Atmos. Chem. Phys., 20, 7801–7827, https://doi.org/10.5194/acp-20-7801-2020, https://doi.org/10.5194/acp-20-7801-2020, 2020
Short summary
Short summary
A new ice nucleation scheme is developed to combine the best features of two previous ice nucleation schemes, so that global models are able to calculate the ice number concentration in both updrafts and downdrafts associated with gravity waves, and has a robust sensitivity to the change of aerosol number. The radiative forcing on cirrus clouds due to anthropogenic emissions is estimated to be −0.20 W m−2, while the inclusion of ice nuclei particles from SOA makes it less negative: −0.04 W m−2.
Qian Huang, Tijian Wang, Pulong Chen, Xiaoxian Huang, Jialei Zhu, and Bingliang Zhuang
Atmos. Chem. Phys., 17, 13457–13471, https://doi.org/10.5194/acp-17-13457-2017, https://doi.org/10.5194/acp-17-13457-2017, 2017
Short summary
Short summary
This paper investigate the important factor contributing to the improvement of air quality of Nanjing, China, during the 2nd Youth Olympic Games, held in August, 2014. The interesting finding is that meteorological factors are not beneficial to air quality during the YOG. However, emission reduction plays a more important role, which suggest that emission reduction is an effective way to cut air pollution levels for social events.
Bingliang Zhuang, Tijian Wang, Jane Liu, Shu Li, Min Xie, Yong Han, Pulong Chen, Qiduo Hu, Xiu-qun Yang, Congbin Fu, and Jialei Zhu
Atmos. Chem. Phys., 17, 1143–1160, https://doi.org/10.5194/acp-17-1143-2017, https://doi.org/10.5194/acp-17-1143-2017, 2017
Short summary
Short summary
The observed near-surface aerosol optical properties in urban Nanjing are analysed from March 2014 to February 2016. Substantial analysis in the key optical properties of the surface aerosol fill the gaps in the study on aerosols in Nanjing, even in the Yangtze River Delta (YRD). Relationships between the aerosol extinction coefficient (single scattering albedo) and atmospheric visibility are also carried out in different seasons to figure out the effect of aerosol on the visibility in Nanjing, YRD.
B. L. Zhuang, T. J. Wang, J. Liu, Y. Ma, C. Q. Yin, S. Li, M. Xie, Y. Han, J. L. Zhu, X. Q. Yang, and C. B. Fu
Atmos. Chem. Phys., 15, 13633–13646, https://doi.org/10.5194/acp-15-13633-2015, https://doi.org/10.5194/acp-15-13633-2015, 2015
Short summary
Short summary
The aerosol absorbing coefficient (AAC) assesses the direct radiative forcing of absorbing aerosols. The corrected AAC and absorption Ångström exponent (AAE) in Nanjing, YRD, are characterized using AE-31. Schmid-corrected AAC at 532nm and the AAE at 660/470nm are about 43.23±28.13 Mm-1 and 1.56, both with strong seasonal and diurnal variations. A high AAC is mostly resultant of local and subregional emissions in Nanjing. It peaks at RH values of 40, 65, and 80% at different AAE levels.
J. Zhu, T. Wang, J. Bieser, and V. Matthias
Atmos. Chem. Phys., 15, 8767–8779, https://doi.org/10.5194/acp-15-8767-2015, https://doi.org/10.5194/acp-15-8767-2015, 2015
Short summary
Short summary
This study estimated the contributions to mercury concentration and deposition in easter China from seven categories of emission sources by CMAQ-Hg. Also, this study focuses on diagnostic and process analyses for atmospheric mercury pollution formation and on identification of the dominant atmospheric processes for mercury.
J. Zhu, T. Wang, R. Talbot, H. Mao, X. Yang, C. Fu, J. Sun, B. Zhuang, S. Li, Y. Han, and M. Xie
Atmos. Chem. Phys., 14, 2233–2244, https://doi.org/10.5194/acp-14-2233-2014, https://doi.org/10.5194/acp-14-2233-2014, 2014
Hua Lu, Min Xie, Bingliang Zhuang, Danyang Ma, Bojun Liu, Yangzhihao Zhan, Tijian Wang, Shu Li, Mengmeng Li, and Kuanguang Zhu
Atmos. Chem. Phys., 24, 8963–8982, https://doi.org/10.5194/acp-24-8963-2024, https://doi.org/10.5194/acp-24-8963-2024, 2024
Short summary
Short summary
To identify cloud, aerosol, and planetary boundary layer (PBL) interactions from an air quality perspective, we summarized two pollution patterns characterized by denser liquid cloud and by obvious cloud radiation interaction (CRI). Numerical simulation experiments showed CRI could cause a 50 % reduction in aerosol radiation interaction (ARI) under a low-trough system. The results emphasized the nonnegligible role of CRI and its inhibition of ARI under wet and cloudy pollution synoptic patterns.
Nanhong Xie, Tijian Wang, Xiaodong Xie, Xu Yue, Filippo Giorgi, Qian Zhang, Danyang Ma, Rong Song, Beiyao Xu, Shu Li, Bingliang Zhuang, Mengmeng Li, Min Xie, Natalya Andreeva Kilifarska, Georgi Gadzhev, and Reneta Dimitrova
Geosci. Model Dev., 17, 3259–3277, https://doi.org/10.5194/gmd-17-3259-2024, https://doi.org/10.5194/gmd-17-3259-2024, 2024
Short summary
Short summary
For the first time, we coupled a regional climate chemistry model, RegCM-Chem, with a dynamic vegetation model, YIBs, to create a regional climate–chemistry–ecology model, RegCM-Chem–YIBs. We applied it to simulate climatic, chemical, and ecological parameters in East Asia and fully validated it on a variety of observational data. Results show that RegCM-Chem–YIBs model is a valuable tool for studying the terrestrial carbon cycle, atmospheric chemistry, and climate change on a regional scale.
Huisheng Bian, Mian Chin, Peter R. Colarco, Eric C. Apel, Donald R. Blake, Karl Froyd, Rebecca S. Hornbrook, Jose Jimenez, Pedro Campuzano Jost, Michael Lawler, Mingxu Liu, Marianne Tronstad Lund, Hitoshi Matsui, Benjamin A. Nault, Joyce E. Penner, Andrew W. Rollins, Gregory Schill, Ragnhild B. Skeie, Hailong Wang, Lu Xu, Kai Zhang, and Jialei Zhu
Atmos. Chem. Phys., 24, 1717–1741, https://doi.org/10.5194/acp-24-1717-2024, https://doi.org/10.5194/acp-24-1717-2024, 2024
Short summary
Short summary
This work studies sulfur in the remote troposphere at global and seasonal scales using aircraft measurements and multi-model simulations. The goal is to understand the sulfur cycle over remote oceans, spread of model simulations, and observation–model discrepancies. Such an understanding and comparison with real observations are crucial to narrow down the uncertainties in model sulfur simulations and improve understanding of the sulfur cycle in atmospheric air quality, climate, and ecosystems.
Hua Lu, Min Xie, Wei Zhao, Bojun Liu, Tijian Wang, and Bingliang Zhuang
Atmos. Meas. Tech., 17, 167–179, https://doi.org/10.5194/amt-17-167-2024, https://doi.org/10.5194/amt-17-167-2024, 2024
Short summary
Short summary
Observations of vertical wind in regions with complex terrain are essential, but they are always sparse and have poor representation. Data verification and quality control are conducted on the wind profile radar and Aeolus wind products in this study, trying to compensate for the limitations of wind field observations. The results shed light on the comprehensive applications of multi-source wind profile data in complicated terrain regions with sparse ground-based wind observations.
Lehui Cui, Yunting Xiao, Wei Hu, Lei Song, Yujue Wang, Chao Zhang, Pingqing Fu, and Jialei Zhu
Earth Syst. Sci. Data, 15, 5403–5425, https://doi.org/10.5194/essd-15-5403-2023, https://doi.org/10.5194/essd-15-5403-2023, 2023
Short summary
Short summary
Isoprene is a crucial non-methane biogenic volatile organic compound with the largest global emissions, which has high chemical reactivity and serves as the primary source of natural secondary organic aerosols. This study built a module to present a 20-year global hourly dataset of marine phytoplankton-generated biological and photochemistry-generated isoprene emissions in the sea microlayers based on the latest advancements in biological, physical, and chemical processes.
Yangzhihao Zhan, Min Xie, Wei Zhao, Tijian Wang, Da Gao, Pulong Chen, Jun Tian, Kuanguang Zhu, Shu Li, Bingliang Zhuang, Mengmeng Li, Yi Luo, and Runqi Zhao
Atmos. Chem. Phys., 23, 9837–9852, https://doi.org/10.5194/acp-23-9837-2023, https://doi.org/10.5194/acp-23-9837-2023, 2023
Short summary
Short summary
Although the main source contribution of pollution is secondary inorganic aerosols in Nanjing, health risks mainly come from industry sources and vehicle emissions. Therefore, the development of megacities should pay more attention to the health burden of vehicle emissions, coal combustion, and industrial processes. This study provides new insight into assessing the relationship between source apportionment and health risks and can provide valuable insight into air pollution strategies.
Danyang Ma, Tijian Wang, Hao Wu, Yawei Qu, Jian Liu, Jane Liu, Shu Li, Bingliang Zhuang, Mengmeng Li, and Min Xie
Atmos. Chem. Phys., 23, 6525–6544, https://doi.org/10.5194/acp-23-6525-2023, https://doi.org/10.5194/acp-23-6525-2023, 2023
Short summary
Short summary
Increasing surface ozone (O3) concentrations have long been a significant environmental issue in China, despite the Clean Air Action Plan launched in 2013. Most previous research ignores the contributions of CO2 variations. Our study comprehensively analyzed O3 variation across China from various perspectives and highlighted the importance of considering CO2 variations when designing long-term O3 control policies, especially in high-vegetation-coverage areas.
Shujun Zhong, Shuang Chen, Junjun Deng, Yanbing Fan, Qiang Zhang, Qiaorong Xie, Yulin Qi, Wei Hu, Libin Wu, Xiaodong Li, Chandra Mouli Pavuluri, Jialei Zhu, Xin Wang, Di Liu, Xiaole Pan, Yele Sun, Zifa Wang, Yisheng Xu, Haijie Tong, Hang Su, Yafang Cheng, Kimitaka Kawamura, and Pingqing Fu
Atmos. Chem. Phys., 23, 2061–2077, https://doi.org/10.5194/acp-23-2061-2023, https://doi.org/10.5194/acp-23-2061-2023, 2023
Short summary
Short summary
This study investigated the role of the secondary organic aerosol (SOA) loading on the molecular composition of wintertime urban aerosols by ultrahigh-resolution mass spectrometry. Results demonstrate that the SOA loading is an important factor associated with the oxidation degree, nitrate group content, and chemodiversity of nitrooxy–organosulfates. Our study also found that the hydrolysis of nitrooxy–organosulfates is a possible pathway for the formation of organosulfates.
Chenchao Zhan, Min Xie, Hua Lu, Bojun Liu, Zheng Wu, Tijian Wang, Bingliang Zhuang, Mengmeng Li, and Shu Li
Atmos. Chem. Phys., 23, 771–788, https://doi.org/10.5194/acp-23-771-2023, https://doi.org/10.5194/acp-23-771-2023, 2023
Short summary
Short summary
With the development of urbanization, urban land use and anthropogenic
emissions increase, affecting urban air quality and, in turn, the health risks associated with air pollutants. In this study, we systematically evaluate the impacts of urbanization on air quality and the corresponding health risks in a highly urbanized city with severe air pollution and complex terrain. This work focuses on the health risks caused by urbanization and can provide valuable insight for air pollution strategies.
Shiyue Zhang, Gang Zeng, Tijian Wang, Xiaoye Yang, and Vedaste Iyakaremye
Atmos. Chem. Phys., 22, 16017–16030, https://doi.org/10.5194/acp-22-16017-2022, https://doi.org/10.5194/acp-22-16017-2022, 2022
Short summary
Short summary
Severe haze days in eastern China (HDEC) are affected by the atmospheric circulation variations on a synoptic scale, while the dominant atmospheric circulation patterns influencing HDEC and the differences between them are still unclear. This study obtains three dominant circulation types that could lead to severe HDEC and investigates the differences between them. The results provide a basis for establishing applicable haze prediction and management policies.
Qirui Zhong, Nick Schutgens, Guido van der Werf, Twan van Noije, Kostas Tsigaridis, Susanne E. Bauer, Tero Mielonen, Alf Kirkevåg, Øyvind Seland, Harri Kokkola, Ramiro Checa-Garcia, David Neubauer, Zak Kipling, Hitoshi Matsui, Paul Ginoux, Toshihiko Takemura, Philippe Le Sager, Samuel Rémy, Huisheng Bian, Mian Chin, Kai Zhang, Jialei Zhu, Svetlana G. Tsyro, Gabriele Curci, Anna Protonotariou, Ben Johnson, Joyce E. Penner, Nicolas Bellouin, Ragnhild B. Skeie, and Gunnar Myhre
Atmos. Chem. Phys., 22, 11009–11032, https://doi.org/10.5194/acp-22-11009-2022, https://doi.org/10.5194/acp-22-11009-2022, 2022
Short summary
Short summary
Aerosol optical depth (AOD) errors for biomass burning aerosol (BBA) are evaluated in 18 global models against satellite datasets. Notwithstanding biases in satellite products, they allow model evaluations. We observe large and diverse model biases due to errors in BBA. Further interpretations of AOD diversities suggest large biases exist in key processes for BBA which require better constraining. These results can contribute to further model improvement and development.
Junjun Deng, Hao Ma, Xinfeng Wang, Shujun Zhong, Zhimin Zhang, Jialei Zhu, Yanbing Fan, Wei Hu, Libin Wu, Xiaodong Li, Lujie Ren, Chandra Mouli Pavuluri, Xiaole Pan, Yele Sun, Zifa Wang, Kimitaka Kawamura, and Pingqing Fu
Atmos. Chem. Phys., 22, 6449–6470, https://doi.org/10.5194/acp-22-6449-2022, https://doi.org/10.5194/acp-22-6449-2022, 2022
Short summary
Short summary
Light-absorbing brown carbon (BrC) plays an important role in climate change and atmospheric chemistry. Here we investigated the seasonal and diurnal variations in water-soluble BrC in PM2.5 in the megacity Tianjin in coastal China. Results of the source apportionments from the combination with organic molecular compositions and optical properties of water-soluble BrC reveal a large contribution from primary bioaerosol particles to BrC in the urban atmosphere.
Mengmeng Li, Zihan Zhang, Quan Yao, Tijian Wang, Min Xie, Shu Li, Bingliang Zhuang, and Yong Han
Atmos. Chem. Phys., 21, 15135–15152, https://doi.org/10.5194/acp-21-15135-2021, https://doi.org/10.5194/acp-21-15135-2021, 2021
Short summary
Short summary
We establish the nonlinear responses between nitrate and NOx in China. Reduction of NOx results in linearly lower nitrate in summer–autumn whereas an increase of winter nitrate until an inflexion point at 40–50 % reduction due to the excess oxidants. NH3 and VOCs are effective in controlling nitrate pollution, whereas decreasing the SO2 and NOx emissions may have counterintuitive effects on nitrate aerosols. This paper helps understand the nonlinear aerosol and photochemistry feedback.
Da Gao, Min Xie, Jane Liu, Tijian Wang, Chaoqun Ma, Haokun Bai, Xing Chen, Mengmeng Li, Bingliang Zhuang, and Shu Li
Atmos. Chem. Phys., 21, 5847–5864, https://doi.org/10.5194/acp-21-5847-2021, https://doi.org/10.5194/acp-21-5847-2021, 2021
Short summary
Short summary
O3 has been increasing in recent years over the Yangtze River Delta region of China and is closely associated with dominant weather systems. Still, the study on the impact of changes in synoptic weather patterns (SWPs) on O3 variation is quite limited. This work aims to reveal the unique features of changes in each SWP under O3 variation and quantifies the effects of meteorological conditions on O3 variation. Our findings could be helpful in strategy planning for O3 pollution control.
Yawei Qu, Apostolos Voulgarakis, Tijian Wang, Matthew Kasoar, Chris Wells, Cheng Yuan, Sunil Varma, and Laura Mansfield
Atmos. Chem. Phys., 21, 5705–5718, https://doi.org/10.5194/acp-21-5705-2021, https://doi.org/10.5194/acp-21-5705-2021, 2021
Short summary
Short summary
The meteorological effect of aerosols on tropospheric ozone is investigated using global atmospheric modelling. We found that aerosol-induced meteorological effects act to reduce modelled ozone concentrations over China, which brings the simulation closer to observed levels. Our work sheds light on understudied processes affecting the levels of tropospheric gaseous pollutants and provides a basis for evaluating such processes using a combination of observations and model sensitivity experiments.
Junjun Deng, Hao Guo, Hongliang Zhang, Jialei Zhu, Xin Wang, and Pingqing Fu
Atmos. Chem. Phys., 20, 14419–14435, https://doi.org/10.5194/acp-20-14419-2020, https://doi.org/10.5194/acp-20-14419-2020, 2020
Short summary
Short summary
One-year source apportionment of BC aerosols in a coastal city in China was conducted with the light-absorption observation-based method and source-oriented model. Source contributions identified by the two source apportionment methods were compared. Temporal variability, potential sources and transport pathways of BC from fossil fuel and biomass burning were characterized. Significant influence of biomass burning in North and East–Central China on BC in the region was highlighted.
Chenchao Zhan, Min Xie, Chongwu Huang, Jane Liu, Tijian Wang, Meng Xu, Chaoqun Ma, Jianwei Yu, Yumeng Jiao, Mengmeng Li, Shu Li, Bingliang Zhuang, Ming Zhao, and Dongyang Nie
Atmos. Chem. Phys., 20, 13781–13799, https://doi.org/10.5194/acp-20-13781-2020, https://doi.org/10.5194/acp-20-13781-2020, 2020
Short summary
Short summary
The Yangtze River Delta (YRD) region has been suffering from severe ozone (O3) pollution in recent years. Synoptic systems, like typhoons, can have a significant effect on O3 episodes. However, research on landfall typhoons affecting O3 in the YRD is limited. This work aims to reveal the main processes of landfall typhoons affecting surface O3 and estimate health impacts of O3 during the study period in the YRD, which can be useful for taking reasonable pollution control measures in this area.
Han Han, Yue Wu, Jane Liu, Tianliang Zhao, Bingliang Zhuang, Honglei Wang, Yichen Li, Huimin Chen, Ye Zhu, Hongnian Liu, Qin'geng Wang, Shu Li, Tijian Wang, Min Xie, and Mengmeng Li
Atmos. Chem. Phys., 20, 13591–13610, https://doi.org/10.5194/acp-20-13591-2020, https://doi.org/10.5194/acp-20-13591-2020, 2020
Short summary
Short summary
Combining simulations from a global chemical transport model and a trajectory model, we find that black carbon aerosols from South Asia and East Asia contribute 77 % of the surface black carbon in the Tibetan Plateau. The Asian monsoon largely modulates inter-annual transport of black carbon from non-local regions to the Tibetan Plateau surface in most seasons, while inter-annual fire activities in South Asia influence black carbon concentration over the Tibetan Plateau surface mainly in spring.
Jialei Zhu and Joyce E. Penner
Atmos. Chem. Phys., 20, 7801–7827, https://doi.org/10.5194/acp-20-7801-2020, https://doi.org/10.5194/acp-20-7801-2020, 2020
Short summary
Short summary
A new ice nucleation scheme is developed to combine the best features of two previous ice nucleation schemes, so that global models are able to calculate the ice number concentration in both updrafts and downdrafts associated with gravity waves, and has a robust sensitivity to the change of aerosol number. The radiative forcing on cirrus clouds due to anthropogenic emissions is estimated to be −0.20 W m−2, while the inclusion of ice nuclei particles from SOA makes it less negative: −0.04 W m−2.
Meng Gao, Zhiwei Han, Zhining Tao, Jiawei Li, Jeong-Eon Kang, Kan Huang, Xinyi Dong, Bingliang Zhuang, Shu Li, Baozhu Ge, Qizhong Wu, Hyo-Jung Lee, Cheol-Hee Kim, Joshua S. Fu, Tijian Wang, Mian Chin, Meng Li, Jung-Hun Woo, Qiang Zhang, Yafang Cheng, Zifa Wang, and Gregory R. Carmichael
Atmos. Chem. Phys., 20, 1147–1161, https://doi.org/10.5194/acp-20-1147-2020, https://doi.org/10.5194/acp-20-1147-2020, 2020
Short summary
Short summary
Topic 3 of the Model Inter-Comparison Study for Asia (MICS-Asia) Phase III examines how online coupled air quality models perform in simulating high aerosol pollution in the North China Plain region during wintertime haze events and evaluates the importance of aerosol radiative feedbacks. This paper discusses the estimates of aerosol radiative forcing, aerosol feedbacks, and possible causes for the differences among the models.
Han Han, Jane Liu, Lei Shu, Tijian Wang, and Huiling Yuan
Atmos. Chem. Phys., 20, 203–222, https://doi.org/10.5194/acp-20-203-2020, https://doi.org/10.5194/acp-20-203-2020, 2020
Short summary
Short summary
We statistically assessed the impacts of local and synoptic meteorology on daily surface ozone in eastern China in summer during 2013–2018. The results show that the meteorology described by a multiple linear regression model explains 43 % of variations in surface ozone. The most important local meteorological factors vary with location in eastern China. The maximum impact of the predominant synoptic pattern on surface ozone can reach ± 8 µg m-3 or ± 16 % of the daily mean over some regions.
Han Han, Jane Liu, Huiling Yuan, Tijian Wang, Bingliang Zhuang, and Xun Zhang
Atmos. Chem. Phys., 19, 12495–12514, https://doi.org/10.5194/acp-19-12495-2019, https://doi.org/10.5194/acp-19-12495-2019, 2019
Short summary
Short summary
In the East Asian middle and upper troposphere, foreign ozone is 0.8–4.8 times more than its native counterpart in all the seasons. At the East Asian surface, the annual mean concentrations of foreign ozone and native ozone are comparable, being approximately 20 ppbv. The seasonal and interannual variations in foreign ozone over East Asia are closely related to the East Asian monsoon.
Huimin Chen, Bingliang Zhuang, Jane Liu, Tijian Wang, Shu Li, Min Xie, Mengmeng Li, Pulong Chen, and Ming Zhao
Atmos. Chem. Phys., 19, 4153–4175, https://doi.org/10.5194/acp-19-4153-2019, https://doi.org/10.5194/acp-19-4153-2019, 2019
Short summary
Short summary
To better understand the characteristics of air pollutants and their interactions in the highly polluted region of eastern China, continuous measurements of particles and trace gases were made during cold seasons in 2016. We found 48 days with excess of PM2.5, 14 with excess of PM10, and 40 with excess of O3. Results further reveal the formation of secondary aerosols under high-O3 and temperature conditions and suggest a VOC-sensitive regime for photochemical production of O3 in urban Nanjing.
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
Short summary
Short summary
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.
Cheng Yuan, William K. M. Lau, Zhanqing Li, and Maureen Cribb
Atmos. Chem. Phys., 19, 1901–1913, https://doi.org/10.5194/acp-19-1901-2019, https://doi.org/10.5194/acp-19-1901-2019, 2019
Short summary
Short summary
Using MERRA-2 reanalysis daily data from 2001 to 2015, we found that during strong South Asian summer monsoon years, the Asian monsoon anticyclone is more expansive and shifted northward. All the CO, carbonaceous aerosols and dust are found to be more abundant in the Asian Tropopause Aerosol Layer (ATAL). ATAL trends are associated with increasing strength of the AMA, with earlier and enhanced vertical transport of ATAL constituents by enhanced overshooting convection over the transport regions.
Meng Gao, Zhiwei Han, Zirui Liu, Meng Li, Jinyuan Xin, Zhining Tao, Jiawei Li, Jeong-Eon Kang, Kan Huang, Xinyi Dong, Bingliang Zhuang, Shu Li, Baozhu Ge, Qizhong Wu, Yafang Cheng, Yuesi Wang, Hyo-Jung Lee, Cheol-Hee Kim, Joshua S. Fu, Tijian Wang, Mian Chin, Jung-Hun Woo, Qiang Zhang, Zifa Wang, and Gregory R. Carmichael
Atmos. Chem. Phys., 18, 4859–4884, https://doi.org/10.5194/acp-18-4859-2018, https://doi.org/10.5194/acp-18-4859-2018, 2018
Short summary
Short summary
Topic 3 of the Model Inter-Comparison Study for Asia (MICS-Asia) Phase III examines how online coupled air quality models perform in simulating high aerosol pollution in the North China Plain region during wintertime haze events and evaluates the importance of aerosol radiative and microphysical feedbacks. A comprehensive overview of the MICS-ASIA III Topic 3 study design is presented.
Bingliang Zhuang, Tijian Wang, Jane Liu, Huizheng Che, Yong Han, Yu Fu, Shu Li, Min Xie, Mengmeng Li, Pulong Chen, Huimin Chen, Xiu-qun Yang, and Jianning Sun
Atmos. Chem. Phys., 18, 1419–1436, https://doi.org/10.5194/acp-18-1419-2018, https://doi.org/10.5194/acp-18-1419-2018, 2018
Short summary
Short summary
Aerosols have a significant influence on climate changes. Their uncertainties could be substantially reduced if observation data were used. The properties and the DRF of fractionated aerosols in the western Yangtze River Delta are investigated based on measurements. Results reveal the characteristics of the optical properties and DRFs of different types of fractionated aerosols, which can be further used to improve aerosol modelling performance in the eastern regions of China.
Qian Huang, Tijian Wang, Pulong Chen, Xiaoxian Huang, Jialei Zhu, and Bingliang Zhuang
Atmos. Chem. Phys., 17, 13457–13471, https://doi.org/10.5194/acp-17-13457-2017, https://doi.org/10.5194/acp-17-13457-2017, 2017
Short summary
Short summary
This paper investigate the important factor contributing to the improvement of air quality of Nanjing, China, during the 2nd Youth Olympic Games, held in August, 2014. The interesting finding is that meteorological factors are not beneficial to air quality during the YOG. However, emission reduction plays a more important role, which suggest that emission reduction is an effective way to cut air pollution levels for social events.
Lei Shu, Min Xie, Da Gao, Tijian Wang, Dexian Fang, Qian Liu, Anning Huang, and Liwen Peng
Atmos. Chem. Phys., 17, 12871–12891, https://doi.org/10.5194/acp-17-12871-2017, https://doi.org/10.5194/acp-17-12871-2017, 2017
Short summary
Short summary
Based on 1-year in situ monitoring data of 16 cities, this paper can enhance the understanding of the pollution characteristics of particles (PM2.5 and PM10) in the Yangtze River Delta region, China. Based on NCEP reanalysis data, the establishment of the potential links between different levels of particle pollution and predominant synoptic patterns can provide an insightful view on formulating pollution control and mitigation strategies.
Min Xie, Lei Shu, Tijian Wang, Da Gao, Shu Li, Bingliang Zhuang, Anning Huang, Dexian Fang, Yong Han, Mengmeng Li, Pulong Chen, Zhijun Liu, Zheng Wu, and Hua Lu
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2017-500, https://doi.org/10.5194/acp-2017-500, 2017
Preprint withdrawn
Short summary
Short summary
The spatial distribution of aerosol can be affected by monsoon circulation. With the aid of a EAWM index, the stong and the weak EAWM years are identified. The long-term trend of weakening EAWM may potentially increase the aerosol loading in YRD, BTH and SCB but decrease AOD in PRD. By using RegCCMS, we further prove that the intensity of EAWM has great impacts on the spatial distribution of aerosols. The change pattern is mainly decided by the change of aerosols in lower troposphere.
Bingliang Zhuang, Tijian Wang, Jane Liu, Shu Li, Min Xie, Yong Han, Pulong Chen, Qiduo Hu, Xiu-qun Yang, Congbin Fu, and Jialei Zhu
Atmos. Chem. Phys., 17, 1143–1160, https://doi.org/10.5194/acp-17-1143-2017, https://doi.org/10.5194/acp-17-1143-2017, 2017
Short summary
Short summary
The observed near-surface aerosol optical properties in urban Nanjing are analysed from March 2014 to February 2016. Substantial analysis in the key optical properties of the surface aerosol fill the gaps in the study on aerosols in Nanjing, even in the Yangtze River Delta (YRD). Relationships between the aerosol extinction coefficient (single scattering albedo) and atmospheric visibility are also carried out in different seasons to figure out the effect of aerosol on the visibility in Nanjing, YRD.
Lei Shu, Min Xie, Tijian Wang, Da Gao, Pulong Chen, Yong Han, Shu Li, Bingliang Zhuang, and Mengmeng Li
Atmos. Chem. Phys., 16, 15801–15819, https://doi.org/10.5194/acp-16-15801-2016, https://doi.org/10.5194/acp-16-15801-2016, 2016
Short summary
Short summary
Severe high ozone episodes usually have close relations to synoptic systems. A regional continuous ozone pollution episode is detected over the Yangtze River Delta region in August 2013. By means of observational analysis and model simulations, it is found that the western Pacific subtropical high and Typhoon Utor play an important role.
Min Xie, Kuanguang Zhu, Tijian Wang, Wen Feng, Da Gao, Mengmeng Li, Shu Li, Bingliang Zhuang, Yong Han, Pulong Chen, and Jingbiao Liao
Atmos. Chem. Phys., 16, 15011–15031, https://doi.org/10.5194/acp-16-15011-2016, https://doi.org/10.5194/acp-16-15011-2016, 2016
Short summary
Short summary
In this paper, we present our new findings on (1) the spatial and temporal characteristics of AH emissions in South China, (2) how to implement the inhomogeneous AH data into the air quality model WRF/Chem, (3) the impacts of AH fluxes on meteorological fields, and (4) the impacts of meteorology changes on the air quality in different cities in South China. Our results show that the meteorology and air pollution predictions in and around big cities are highly sensitive to AH.
Min Xie, Jingbiao Liao, Tijian Wang, Kuanguang Zhu, Bingliang Zhuang, Yong Han, Mengmeng Li, and Shu Li
Atmos. Chem. Phys., 16, 6071–6089, https://doi.org/10.5194/acp-16-6071-2016, https://doi.org/10.5194/acp-16-6071-2016, 2016
Short summary
Short summary
The spatial and temporal distribution of anthropogenic heat emissions over the YRD region was developed. These gridded AH emissions were incorporated into the modified WRF/Chem model with the seasonal and diurnal variation. The impacts of AH on meteorology and chemical variables were evaluated. The results show that the anthropogenic heat inputs improved the meteorology and air pollution predictions from WRF/Chem in and around large urban areas.
B. L. Zhuang, T. J. Wang, J. Liu, Y. Ma, C. Q. Yin, S. Li, M. Xie, Y. Han, J. L. Zhu, X. Q. Yang, and C. B. Fu
Atmos. Chem. Phys., 15, 13633–13646, https://doi.org/10.5194/acp-15-13633-2015, https://doi.org/10.5194/acp-15-13633-2015, 2015
Short summary
Short summary
The aerosol absorbing coefficient (AAC) assesses the direct radiative forcing of absorbing aerosols. The corrected AAC and absorption Ångström exponent (AAE) in Nanjing, YRD, are characterized using AE-31. Schmid-corrected AAC at 532nm and the AAE at 660/470nm are about 43.23±28.13 Mm-1 and 1.56, both with strong seasonal and diurnal variations. A high AAC is mostly resultant of local and subregional emissions in Nanjing. It peaks at RH values of 40, 65, and 80% at different AAE levels.
J. Zhu, T. Wang, J. Bieser, and V. Matthias
Atmos. Chem. Phys., 15, 8767–8779, https://doi.org/10.5194/acp-15-8767-2015, https://doi.org/10.5194/acp-15-8767-2015, 2015
Short summary
Short summary
This study estimated the contributions to mercury concentration and deposition in easter China from seven categories of emission sources by CMAQ-Hg. Also, this study focuses on diagnostic and process analyses for atmospheric mercury pollution formation and on identification of the dominant atmospheric processes for mercury.
H. Che, X.-Y. Zhang, X. Xia, P. Goloub, B. Holben, H. Zhao, Y. Wang, X.-C. Zhang, H. Wang, L. Blarel, B. Damiri, R. Zhang, X. Deng, Y. Ma, T. Wang, F. Geng, B. Qi, J. Zhu, J. Yu, Q. Chen, and G. Shi
Atmos. Chem. Phys., 15, 7619–7652, https://doi.org/10.5194/acp-15-7619-2015, https://doi.org/10.5194/acp-15-7619-2015, 2015
Short summary
Short summary
This work studied more than 10 years of measurements of aerosol optical depths (AODs) made for 50 sites of CARSNET compiled into a climatology of aerosol optical properties for China. It lets us see a detailed full-scale description of AOD observations over China. The results would benefit us a lot in comprehending the temporal and special distribution aerosol optical property over China. Also the data would be valuable to communities of aerosol satellite retrieval, modelling, etc.
J. Zhu, T. Wang, R. Talbot, H. Mao, X. Yang, C. Fu, J. Sun, B. Zhuang, S. Li, Y. Han, and M. Xie
Atmos. Chem. Phys., 14, 2233–2244, https://doi.org/10.5194/acp-14-2233-2014, https://doi.org/10.5194/acp-14-2233-2014, 2014
L. Xing, T.-M. Fu, J. J. Cao, S. C. Lee, G. H. Wang, K. F. Ho, M.-C. Cheng, C.-F. You, and T. J. Wang
Atmos. Chem. Phys., 13, 4307–4318, https://doi.org/10.5194/acp-13-4307-2013, https://doi.org/10.5194/acp-13-4307-2013, 2013
Related subject area
Subject: Gases | Research Activity: Field Measurements | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Biomass-burning sources control ambient particulate matter, but traffic and industrial sources control volatile organic compound (VOC) emissions and secondary-pollutant formation during extreme pollution events in Delhi
Multi-year observations of variable incomplete combustion in the New York megacity
Observations of the vertical distributions of summertime atmospheric pollutants in Nam Co: OH production and source analysis
Measurement report: Elevated atmospheric ammonia may promote particle pH and HONO formation – insights from the COVID-19 pandemic
Measurement report: Vertical and temporal variability in the near-surface ozone production rate and sensitivity in an urban area in the Pearl River Delta region, China
Elevated oxidized mercury in the free troposphere: analytical advances and application at a remote continental mountaintop site
Using observed urban NOx sinks to constrain VOC reactivity and the ozone and radical budget in the Seoul Metropolitan Area
Real-world emission characteristics of VOCs from typical cargo ships and their potential contributions to secondary organic aerosol and O3 under low-sulfur fuel policies
NO3 reactivity during a summer period in a temperate forest below and above the canopy
The role of oceanic ventilation and terrestrial outflow in atmospheric non-methane hydrocarbons over the Chinese marginal seas
Concentration and source changes of nitrous acid (HONO) during the COVID-19 lockdown in Beijing
Characteristics and sources of nonmethane volatile organic compounds (NMVOCs) and O3–NOx–NMVOC relationships in Zhengzhou, China
Deciphering anthropogenic and biogenic contributions to selected non-methane volatile organic compound emissions in an urban area
Emission characteristics of reactive organic gases (ROGs) from industrial volatile chemical products (VCPs) in the Pearl River Delta (PRD), China
Measurement report: Enhanced photochemical formation of formic and isocyanic acids in urban regions aloft – insights from tower-based online gradient measurements
Sources of organic gases and aerosol particles and their roles in nighttime particle growth at a rural forested site in southwest Germany
Surface snow bromide and nitrate at Eureka, Canada, in early spring and implications for polar boundary layer chemistry
Opinion: Strengthening research in the Global South – atmospheric science opportunities in South America and Africa
Measurement Report: Urban Ammonia and Amines in Houston, Texas
Analysis of ozone vertical profile day-to-day variability in the lower troposphere during the Paris-2022 ACROSS campaign
Consistency evaluation of tropospheric ozone from ozonesonde and IAGOS aircraft observations: vertical distribution, ozonesonde types and station-airport distance
Investigating Carbonyl Compounds above the Amazon Rainforest using PTR-ToF-MS with NO+ Chemical Ionization
Shipping and algae emissions have a major impact on ambient air mixing ratios of non-methane hydrocarbons (NMHCs) and methanethiol on Utö Island in the Baltic Sea
Contribution of cooking emissions to the urban volatile organic compounds in Las Vegas, NV
Reanalysis of NOAA H2 observations: implications for the H2 budget
A large role of missing volatile organic compound reactivity from anthropogenic emissions in ozone pollution regulation
Measurement report: Insights into the chemical composition and origin of molecular clusters and potential precursor molecules present in the free troposphere over the southern Indian Ocean: observations from the Maïdo Observatory (2150 m a.s.l., Réunion)
Ozone deposition measurements over wheat fields in the North China Plain: variability and related factors of deposition flux and velocity
Production of oxygenated volatile organic compounds from the ozonolysis of coastal seawater
Comment on “Transport of substantial stratospheric ozone to the surface by a dying typhoon and shallow convection” by Chen et al. (2022)
Observations of cyanogen bromide (BrCN) in the global troposphere and their relation to polar surface O3 destruction
CO2 and CO temporal variability over Mexico City from ground-based total column and surface measurements
Individual coal mine methane emissions constrained by eddy covariance measurements: low bias and missing sources
Discovery of reactive chlorine, sulphur and nitrogen containing ambient volatile organic compounds in the megacity of Delhi during both clean and extremely polluted seasons
Measurement report: In-flight and ground-based measurements of nitrogen oxide emissions from latest generation jet engines and 100% sustainable aviation fuel
Measurement report: Observations of ground-level ozone concentration gradients perpendicular to the Lake Ontario shoreline
Measurement report: The Palau Atmospheric Observatory and its ozonesonde record – continuous monitoring of tropospheric composition and dynamics in the tropical western Pacific
Quantifying SO2 oxidation pathways to atmospheric sulfate using stable sulfur and oxygen isotopes: laboratory simulation and field observation
Influences of downward transport and photochemistry on surface ozone over East Antarctica during austral summer: in situ observations and model simulations
Iodine oxoacids and their roles in sub-3 nm particle growth in polluted urban environments
Intensive photochemical oxidation in the marine atmosphere: evidence from direct radical measurements
Diurnal variations in oxygen and nitrogen isotopes of atmospheric nitrogen dioxide and nitrate: implications for tracing NOx oxidation pathways and emission sources
Measurement report: Method for evaluating CO2 emissions from a cement plant using atmospheric δ(O2 ∕ N2) and CO2 measurements and its implication for future detection of CO2 capture signals
Aircraft-based mass balance estimate of methane emissions from offshore gas facilities in the southern North Sea
Measurement report: Sources, sinks and lifetime of NOX in a sub-urban temperate forest at night
Parameterizations of US wildfire and prescribed fire emission ratios and emission factors based on FIREX-AQ aircraft measurements
Measurement report: Atmospheric nitrate radical chemistry in the South China Sea influenced by the urban outflow of the Pearl River Delta
The interhemispheric gradient of SF6 in the upper troposphere
Weather regimes and the related atmospheric composition at a Pyrenean observatory characterized by hierarchical clustering of a 5-year data set
Tropospheric bromine monoxide vertical profiles retrieved across the Alaskan Arctic in springtime
Arpit Awasthi, Baerbel Sinha, Haseeb Hakkim, Sachin Mishra, Varkrishna Mummidivarapu, Gurmanjot Singh, Sachin D. Ghude, Vijay Kumar Soni, Narendra Nigam, Vinayak Sinha, and Madhavan N. Rajeevan
Atmos. Chem. Phys., 24, 10279–10304, https://doi.org/10.5194/acp-24-10279-2024, https://doi.org/10.5194/acp-24-10279-2024, 2024
Short summary
Short summary
We use 111 volatile organic compounds (VOCs), PM10, and PM2.5 in a positive matrix factorization (PMF) model to resolve 11 pollution sources validated with chemical fingerprints. Crop residue burning and heating account for ~ 50 % of the PM, while traffic and industrial emissions dominate the gas-phase VOC burden and formation potential of secondary organic aerosols (> 60 %). Non-tailpipe emissions from compressed-natural-gas-fuelled commercial vehicles dominate the transport sector's PM burden.
Luke D. Schiferl, Cong Cao, Bronte Dalton, Andrew Hallward-Driemeier, Ricardo Toledo-Crow, and Róisín Commane
Atmos. Chem. Phys., 24, 10129–10142, https://doi.org/10.5194/acp-24-10129-2024, https://doi.org/10.5194/acp-24-10129-2024, 2024
Short summary
Short summary
Carbon monoxide (CO) is an air pollutant and an important indicator of the incomplete combustion of fossil fuels in cities. Using 4 years of winter and spring observations in New York City, we found that both the magnitude and variability of CO from the metropolitan area are greater than expected. Transportation emissions cannot explain the missing and variable CO, which points to energy from buildings as a likely underappreciated source of urban air pollution and greenhouse gas emissions.
Chengzhi Xing, Cheng Liu, Chunxiang Ye, Jingkai Xue, Hongyu Wu, Xiangguang Ji, Jinping Ou, and Qihou Hu
Atmos. Chem. Phys., 24, 10093–10112, https://doi.org/10.5194/acp-24-10093-2024, https://doi.org/10.5194/acp-24-10093-2024, 2024
Short summary
Short summary
We identified the contributions of ozone (O3) and nitrous acid (HONO) to the production rates of hydroxide (OH) in vertical space on the Tibetan Plateau (TP). A new insight was offered: the contributions of HONO and O3 to the production rates of OH on the TP are even greater than in lower-altitudes areas. This study enriches the understanding of vertical distribution of atmospheric components and explains the strong atmospheric oxidation capacity (AOC) on the TP.
Xinyuan Zhang, Lingling Wang, Nan Wang, Shuangliang Ma, Shenbo Wang, Ruiqin Zhang, Dong Zhang, Mingkai Wang, and Hongyu Zhang
Atmos. Chem. Phys., 24, 9885–9898, https://doi.org/10.5194/acp-24-9885-2024, https://doi.org/10.5194/acp-24-9885-2024, 2024
Short summary
Short summary
This study highlights the importance of the redox reaction of NO2 with SO2 based on actual atmospheric observations. The particle pH in future China is expected to rise steadily. Consequently, this reaction could become a significant source of HONO in China. Therefore, it is crucial to coordinate the control of SO2, NOx, and NH3 emissions to avoid a rapid increase in the particle pH.
Jun Zhou, Chunsheng Zhang, Aiming Liu, Bin Yuan, Yan Wang, Wenjie Wang, Jie-Ping Zhou, Yixin Hao, Xiao-Bing Li, Xianjun He, Xin Song, Yubin Chen, Suxia Yang, Shuchun Yang, Yanfeng Wu, Bin Jiang, Shan Huang, Junwen Liu, Yuwen Peng, Jipeng Qi, Minhui Deng, Bowen Zhong, Yibo Huangfu, and Min Shao
Atmos. Chem. Phys., 24, 9805–9826, https://doi.org/10.5194/acp-24-9805-2024, https://doi.org/10.5194/acp-24-9805-2024, 2024
Short summary
Short summary
In-depth understanding of the near-ground vertical variability in photochemical ozone (O3) formation is crucial for mitigating O3 pollution. Utilizing a self-built vertical observation system, a direct net photochemical O3 production rate detection system, and an observation-based model, we diagnosed the vertical distributions and formation mechanism of net photochemical O3 production rates and sensitivity in the Pearl River Delta region, one of the most O3-polluted areas in China.
Eleanor J. Derry, Tyler R. Elgiar, Taylor Y. Wilmot, Nicholas W. Hoch, Noah S. Hirshorn, Peter Weiss-Penzias, Christopher F. Lee, John C. Lin, A. Gannet Hallar, Rainer Volkamer, Seth N. Lyman, and Lynne E. Gratz
Atmos. Chem. Phys., 24, 9615–9643, https://doi.org/10.5194/acp-24-9615-2024, https://doi.org/10.5194/acp-24-9615-2024, 2024
Short summary
Short summary
Mercury (Hg) is a globally distributed neurotoxic pollutant. Atmospheric deposition is the main source of Hg in ecosystems. However, measurement biases hinder understanding of the origins and abundance of the more bioavailable oxidized form. We used an improved, calibrated measurement system to study air mass composition and transport of atmospheric Hg at a remote mountaintop site in the central US. Oxidized Hg originated upwind in the low to middle free troposphere under clean, dry conditions.
Benjamin A. Nault, Katherine R. Travis, James H. Crawford, Donald R. Blake, Pedro Campuzano-Jost, Ronald C. Cohen, Joshua P. DiGangi, Glenn S. Diskin, Samuel R. Hall, L. Gregory Huey, Jose L. Jimenez, Kyung-Eun Min, Young Ro Lee, Isobel J. Simpson, Kirk Ullmann, and Armin Wisthaler
Atmos. Chem. Phys., 24, 9573–9595, https://doi.org/10.5194/acp-24-9573-2024, https://doi.org/10.5194/acp-24-9573-2024, 2024
Short summary
Short summary
Ozone (O3) is a pollutant formed from the reactions of gases emitted from various sources. In urban areas, the density of human activities can increase the O3 formation rate (P(O3)), thus impacting air quality and health. Observations collected over Seoul, South Korea, are used to constrain P(O3). A high local P(O3) was found; however, local P(O3) was partly reduced due to compounds typically ignored. These observations also provide constraints for unmeasured compounds that will impact P(O3).
Fan Zhang, Binyu Xiao, Zeyu Liu, Yan Zhang, Chongguo Tian, Rui Li, Can Wu, Yali Lei, Si Zhang, Xinyi Wan, Yubao Chen, Yong Han, Min Cui, Cheng Huang, Hongli Wang, Yingjun Chen, and Gehui Wang
Atmos. Chem. Phys., 24, 8999–9017, https://doi.org/10.5194/acp-24-8999-2024, https://doi.org/10.5194/acp-24-8999-2024, 2024
Short summary
Short summary
Mandatory use of low-sulfur fuel due to global sulfur limit regulations means large uncertainties in volatile organic compound (VOC) emissions. On-board tests of VOCs from nine cargo ships in China were carried out. Results showed that switching from heavy-fuel oil to diesel increased emission factor VOCs by 48 % on average, enhancing O3 and the secondary organic aerosol formation potential. Thus, implementing a global ultra-low-sulfur oil policy needs to be optimized in the near future.
Patrick Dewald, Tobias Seubert, Simone T. Andersen, Gunther N. T. E. Türk, Jan Schuladen, Max R. McGillen, Cyrielle Denjean, Jean-Claude Etienne, Olivier Garrouste, Marina Jamar, Sergio Harb, Manuela Cirtog, Vincent Michoud, Mathieu Cazaunau, Antonin Bergé, Christopher Cantrell, Sebastien Dusanter, Bénédicte Picquet-Varrault, Alexandre Kukui, Chaoyang Xue, Abdelwahid Mellouki, Jos Lelieveld, and John N. Crowley
Atmos. Chem. Phys., 24, 8983–8997, https://doi.org/10.5194/acp-24-8983-2024, https://doi.org/10.5194/acp-24-8983-2024, 2024
Short summary
Short summary
In the scope of a field campaign in a suburban forest near Paris in the summer of 2022, we measured the reactivity of the nitrate radical NO3 towards biogenic volatile organic compounds (BVOCs; e.g. monoterpenes) mainly below but also above the canopy. NO3 reactivity was the highest during nights with strong temperature inversions and decreased strongly with height. Reactions with BVOCs were the main removal process of NO3 throughout the diel cycle below the canopy.
Jian Wang, Lei Xue, Qianyao Ma, Feng Xu, Gaobin Xu, Shibo Yan, Jiawei Zhang, Jianlong Li, Honghai Zhang, Guiling Zhang, and Zhaohui Chen
Atmos. Chem. Phys., 24, 8721–8736, https://doi.org/10.5194/acp-24-8721-2024, https://doi.org/10.5194/acp-24-8721-2024, 2024
Short summary
Short summary
This study investigated the distribution and sources of non-methane hydrocarbons (NMHCs) in the lower atmosphere over the marginal seas of China. NMHCs, a subset of volatile organic compounds (VOCs), play a crucial role in atmospheric chemistry. Derived from systematic atmospheric sampling in coastal cities and marginal sea regions, this study offers valuable insights into the interaction between land and sea in shaping offshore atmospheric NMHCs.
Yusheng Zhang, Feixue Zheng, Zemin Feng, Chaofan Lian, Weigang Wang, Xiaolong Fan, Wei Ma, Zhuohui Lin, Chang Li, Gen Zhang, Chao Yan, Ying Zhang, Veli-Matti Kerminen, Federico Bianch, Tuukka Petäjä, Juha Kangasluoma, Markku Kulmala, and Yongchun Liu
Atmos. Chem. Phys., 24, 8569–8587, https://doi.org/10.5194/acp-24-8569-2024, https://doi.org/10.5194/acp-24-8569-2024, 2024
Short summary
Short summary
The nitrous acid (HONO) budget was validated during a COVID-19 lockdown event. The main conclusions are (1) HONO concentrations showed a significant decrease from 0.97 to 0.53 ppb during lockdown; (2) vehicle emissions accounted for 53 % of nighttime sources, with the heterogeneous conversion of NO2 on ground surfaces more important than aerosol; and (3) the dominant daytime source shifted from the homogenous reaction between NO and OH (51 %) to nitrate photolysis (53 %) during lockdown.
Dong Zhang, Xiao Li, Minghao Yuan, Yifei Xu, Qixiang Xu, Fangcheng Su, Shenbo Wang, and Ruiqin Zhang
Atmos. Chem. Phys., 24, 8549–8567, https://doi.org/10.5194/acp-24-8549-2024, https://doi.org/10.5194/acp-24-8549-2024, 2024
Short summary
Short summary
The increasing concentration of O3 precursors and unfavorable meteorological conditions are key factors in the formation of O3 pollution in Zhengzhou. Vehicular exhausts (28 %), solvent usage (27 %), and industrial production (22 %) are identified as the main sources of NMVOCs. Moreover, O3 formation in Zhengzhou is found to be in an anthropogenic volatile organic compound (AVOC)-limited regime. Thus, to reduce O3 formation, a minimum AVOCs / NOx reduction ratio ≥ 3 : 1 is recommended.
Arianna Peron, Martin Graus, Marcus Striednig, Christian Lamprecht, Georg Wohlfahrt, and Thomas Karl
Atmos. Chem. Phys., 24, 7063–7083, https://doi.org/10.5194/acp-24-7063-2024, https://doi.org/10.5194/acp-24-7063-2024, 2024
Short summary
Short summary
The anthropogenic fraction of non-methane volatile organic compound (NMVOC) emissions associated with biogenic sources (e.g., terpenes) is investigated based on eddy covariance observations. The anthropogenic fraction of terpene emissions is strongly dependent on season. When analyzing volatile chemical product (VCP) emissions in urban environments, we caution that observations from short-term campaigns might over-/underestimate their significance depending on local and seasonal circumstances.
Sihang Wang, Bin Yuan, Xianjun He, Ru Cui, Xin Song, Yubin Chen, Caihong Wu, Chaomin Wang, Yibo Huangfu, Xiao-Bing Li, Boguang Wang, and Min Shao
Atmos. Chem. Phys., 24, 7101–7121, https://doi.org/10.5194/acp-24-7101-2024, https://doi.org/10.5194/acp-24-7101-2024, 2024
Short summary
Short summary
Emissions of reactive organic gases from industrial volatile chemical product sources are measured. There are large differences among these industrial sources. We show that oxygenated species account for significant contributions to reactive organic gas emissions, especially for industrial sources utilizing water-borne chemicals.
Qing Yang, Xiao-Bing Li, Bin Yuan, Xiaoxiao Zhang, Yibo Huangfu, Lei Yang, Xianjun He, Jipeng Qi, and Min Shao
Atmos. Chem. Phys., 24, 6865–6882, https://doi.org/10.5194/acp-24-6865-2024, https://doi.org/10.5194/acp-24-6865-2024, 2024
Short summary
Short summary
Online vertical gradient measurements of formic and isocyanic acids were made based on a 320 m tower in a megacity. Vertical variations and sources of the two acids were analyzed in this study. We find that formic and isocyanic acids exhibited positive vertical gradients and were mainly contributed by photochemical formations. The formation of formic and isocyanic acids was also significantly enhanced in urban regions aloft.
Junwei Song, Harald Saathoff, Feng Jiang, Linyu Gao, Hengheng Zhang, and Thomas Leisner
Atmos. Chem. Phys., 24, 6699–6717, https://doi.org/10.5194/acp-24-6699-2024, https://doi.org/10.5194/acp-24-6699-2024, 2024
Short summary
Short summary
This study presents concurrent online measurements of organic gas and particles (VOCs and OA) at a forested site in summer. Both VOCs and OA were largely contributed by oxygenated organic compounds. Semi-volatile oxygenated OA and organic nitrate formed from monoterpenes and sesquiterpenes contributed significantly to nighttime particle growth. The results help us to understand the causes of nighttime particle growth regularly observed in summer in central European rural forested environments.
Xin Yang, Kimberly Strong, Alison S. Criscitiello, Marta Santos-Garcia, Kristof Bognar, Xiaoyi Zhao, Pierre Fogal, Kaley A. Walker, Sara M. Morris, and Peter Effertz
Atmos. Chem. Phys., 24, 5863–5886, https://doi.org/10.5194/acp-24-5863-2024, https://doi.org/10.5194/acp-24-5863-2024, 2024
Short summary
Short summary
This study uses snow samples collected from a Canadian high Arctic site, Eureka, to demonstrate that surface snow in early spring is a net sink of atmospheric bromine and nitrogen. Surface snow bromide and nitrate are significantly correlated, indicating the oxidation of reactive nitrogen is accelerated by reactive bromine. In addition, we show evidence that snow photochemical release of reactive bromine is very weak, and its emission flux is much smaller than the deposition flux of bromide.
Rebecca M. Garland, Katye E. Altieri, Laura Dawidowski, Laura Gallardo, Aderiana Mbandi, Nestor Y. Rojas, and N'datchoh E. Touré
Atmos. Chem. Phys., 24, 5757–5764, https://doi.org/10.5194/acp-24-5757-2024, https://doi.org/10.5194/acp-24-5757-2024, 2024
Short summary
Short summary
This opinion piece focuses on two geographical areas in the Global South where the authors are based that are underrepresented in atmospheric science. This opinion provides context on common challenges and constraints, with suggestions on how the community can address these. The focus is on the strengths of atmospheric science research in these regions. It is these strengths, we believe, that highlight the critical role of Global South researchers in the future of atmospheric science research.
Lee Tiszenkel, James Flynn, and Shan-Hu Lee
EGUsphere, https://doi.org/10.5194/egusphere-2024-1230, https://doi.org/10.5194/egusphere-2024-1230, 2024
Short summary
Short summary
Ammonia and amines are important ingredients for aerosol formation in urban environments, but the measurements of these compounds are extremely challenging. Our observations show that urban ammonia and amines in Houston are emitted from urban sources and diurnal variations of their concentrations are governed by gas-to-particle conversion processes.
Gerard Ancellet, Camille Viatte, Anne Boynard, François Ravetta, Jacques Pelon, Cristelle Cailteau-Fischbach, Pascal Genau, Julie Capo, Axel Roy, and Philippe Nédélec
EGUsphere, https://doi.org/10.5194/egusphere-2024-892, https://doi.org/10.5194/egusphere-2024-892, 2024
Short summary
Short summary
Characterization of ozone pollution in urban areas has benefited from a measurement campaign in summer 2022 in the Paris region. The analysis is based on 21 days of lidar and aircraft observations. The main objective is a sensitivity analysis of ozone pollution to first the micrometeorological processes in the urban atmospheric boundary layer, and second, the transport of regional pollution. The paper also discuss to what extent satellite observations can track the observed ozone plumes.
Honglei Wang, David W. Tarasick, Jane Liu, Herman G. J. Smit, Roeland Van Malderen, Lijuan Shen, and Tianliang Zhao
EGUsphere, https://doi.org/10.5194/egusphere-2024-1015, https://doi.org/10.5194/egusphere-2024-1015, 2024
Short summary
Short summary
In this study, we identify 23 suitable pairs of sites in the WOUDC and IAGOS datasets from 1995 to 2021, compare the average vertical distribution of tropospheric O3 shown by ozonesonde and aircraft measurements, and analyze their differences by ozonesonde type and by station-airport distance.
Akima Ringsdorf, Achim Edtbauer, Bruna Holanda, Christopher Poehlker, Marta O. Sá, Alessandro Araújo, Jürgen Kesselmeier, Jos Lelieveld, and Jonathan Williams
EGUsphere, https://doi.org/10.5194/egusphere-2024-1210, https://doi.org/10.5194/egusphere-2024-1210, 2024
Short summary
Short summary
We show the average height distribution of separately observed aldehydes and ketones over a day and discuss their rainforest-specific sources and sinks and their seasonal changes above the Amazon rainforest. Ketones have much longer atmospheric lifetimes than aldehydes, and thus different implications for atmospheric chemistry. However, they are commonly observed together, which we overcome by measuring with a NO+ chemical ionization mass spectrometer for the first time in the Amazon rainforest.
Heidi Hellén, Rostislav Kouznetsov, Kaisa Kraft, Jukka Seppälä, Mika Vestenius, Jukka-Pekka Jalkanen, Lauri Laakso, and Hannele Hakola
Atmos. Chem. Phys., 24, 4717–4731, https://doi.org/10.5194/acp-24-4717-2024, https://doi.org/10.5194/acp-24-4717-2024, 2024
Short summary
Short summary
Mixing ratios of C2-C5 NMHCs and methanethiol were measured on an island in the Baltic Sea using an in situ gas chromatograph. Shipping emissions were found to be an important source of ethene, ethyne, propene, and benzene. High summertime mixing ratios of methanethiol and dependence of mixing ratios on seawater temperature and height indicated the biogenic origin to possibly be phytoplankton or macroalgae. These emissions may have a strong impact on SO2 production and new particle formation.
Matthew M. Coggon, Chelsea E. Stockwell, Lu Xu, Jeff Peischl, Jessica B. Gilman, Aaron Lamplugh, Henry J. Bowman, Kenneth Aikin, Colin Harkins, Qindan Zhu, Rebecca H. Schwantes, Jian He, Meng Li, Karl Seltzer, Brian McDonald, and Carsten Warneke
Atmos. Chem. Phys., 24, 4289–4304, https://doi.org/10.5194/acp-24-4289-2024, https://doi.org/10.5194/acp-24-4289-2024, 2024
Short summary
Short summary
Residential and commercial cooking emits pollutants that degrade air quality. Here, ambient observations show that cooking is an important contributor to anthropogenic volatile organic compounds (VOCs) emitted in Las Vegas, NV. These emissions are not fully presented in air quality models, and more work may be needed to quantify emissions from important sources, such as commercial restaurants.
Fabien Paulot, Gabrielle Pétron, Andrew M. Crotwell, and Matteo B. Bertagni
Atmos. Chem. Phys., 24, 4217–4229, https://doi.org/10.5194/acp-24-4217-2024, https://doi.org/10.5194/acp-24-4217-2024, 2024
Short summary
Short summary
New data from the National Oceanic and Atmospheric Administration show that hydrogen (H2) concentrations increased from 2010 to 2019, which is consistent with the simulated increase in H2 photochemical production (mainly from methane). But this cannot be reconciled with the expected decrease (increase) in H2 anthropogenic emissions (soil deposition) in the same period. This shows gaps in our knowledge of the H2 biogeochemical cycle that must be resolved to quantify the impact of higher H2 usage.
Wenjie Wang, Bin Yuan, Hang Su, Yafang Cheng, Jipeng Qi, Sihang Wang, Wei Song, Xinming Wang, Chaoyang Xue, Chaoqun Ma, Fengxia Bao, Hongli Wang, Shengrong Lou, and Min Shao
Atmos. Chem. Phys., 24, 4017–4027, https://doi.org/10.5194/acp-24-4017-2024, https://doi.org/10.5194/acp-24-4017-2024, 2024
Short summary
Short summary
This study investigates the important role of unmeasured volatile organic compounds (VOCs) in ozone formation. Based on results in a megacity of China, we show that unmeasured VOCs can contribute significantly to ozone fomation and also influence the determination of ozone control strategy. Our results show that these unmeasured VOCs are mainly from human sources.
Romain Salignat, Matti Rissanen, Siddharth Iyer, Jean-Luc Baray, Pierre Tulet, Jean-Marc Metzger, Jérôme Brioude, Karine Sellegri, and Clémence Rose
Atmos. Chem. Phys., 24, 3785–3812, https://doi.org/10.5194/acp-24-3785-2024, https://doi.org/10.5194/acp-24-3785-2024, 2024
Short summary
Short summary
Using mass spectrometry data collected at the Maïdo Observatory (2160 m a.s.l., Réunion), we provide the first detailed analysis of molecular cluster chemical composition specifically in the marine free troposphere. The abundance of the identified species is related both to in situ meteorological parameters and air mass history, which also provide insight into their origin. Our work makes an important contribution to documenting the chemistry and physics of the marine free troposphere.
Xiaoyi Zhang, Wanyun Xu, Weili Lin, Gen Zhang, Jinjian Geng, Li Zhou, Huarong Zhao, Sanxue Ren, Guangsheng Zhou, Jianmin Chen, and Xiaobin Xu
EGUsphere, https://doi.org/10.5194/egusphere-2024-643, https://doi.org/10.5194/egusphere-2024-643, 2024
Short summary
Short summary
Ozone (O3) deposition is a key process removing surface O3, affecting air quality, ecosystem and climate change. This study conducted an O3 deposition measurement over wheat canopy using a newly relaxed eddy accumulation flux system. Large variabilities of O3 deposition were detected mainly determined by crop growth and modulated by various environmental factors. More O3 deposition observations over different surfaces are needed for exploring deposition mechanism, model optimization.
Delaney B. Kilgour, Gordon A. Novak, Megan S. Claflin, Brian M. Lerner, and Timothy H. Bertram
Atmos. Chem. Phys., 24, 3729–3742, https://doi.org/10.5194/acp-24-3729-2024, https://doi.org/10.5194/acp-24-3729-2024, 2024
Short summary
Short summary
Laboratory experiments with seawater mimics suggest ozone deposition to the surface ocean can be a source of reactive carbon to the marine atmosphere. We conduct both field and laboratory measurements to assess abiotic VOC composition and yields from ozonolysis of real surface seawater. We show that C5–C11 aldehydes contribute to the observed VOC emission flux. We estimate that VOCs generated by the ozonolysis of surface seawater are competitive with biological VOC production and emission.
Xiangdong Zheng, Wen Yang, Yuting Sun, Chunmei Geng, Yingying Liu, and Xiaobin Xu
Atmos. Chem. Phys., 24, 3759–3768, https://doi.org/10.5194/acp-24-3759-2024, https://doi.org/10.5194/acp-24-3759-2024, 2024
Short summary
Short summary
Chen et al. (2022) attributed the nocturnal ozone enhancement (NOE) during the night of 31 July 2021 in the North China Plain (NCP) to "the direct stratospheric intrusion to reach the surface". We analyzed in situ data from the NCP. Our results do not suggest that there was a significant impact from the stratosphere on surface ozone during the NOE. We argue that the NOE was not caused by stratospheric intrusion but originated from fresh photochemical production in the lower troposphere.
James M. Roberts, Siyuan Wang, Patrick R. Veres, J. Andrew Neuman, Michael A. Robinson, Ilann Bourgeois, Jeff Peischl, Thomas B. Ryerson, Chelsea R. Thompson, Hannah M. Allen, John D. Crounse, Paul O. Wennberg, Samuel R. Hall, Kirk Ullmann, Simone Meinardi, Isobel J. Simpson, and Donald Blake
Atmos. Chem. Phys., 24, 3421–3443, https://doi.org/10.5194/acp-24-3421-2024, https://doi.org/10.5194/acp-24-3421-2024, 2024
Short summary
Short summary
We measured cyanogen bromide (BrCN) in the troposphere for the first time. BrCN is a product of the same active bromine chemistry that destroys ozone and removes mercury in polar surface environments and is a previously unrecognized sink for active Br compounds. BrCN has an apparent lifetime against heterogeneous loss in the range 1–10 d, so it serves as a cumulative marker of Br-radical chemistry. Accounting for BrCN chemistry is an important part of understanding polar Br cycling.
Noémie Taquet, Wolfgang Stremme, María Eugenia Gonzalez del Castillo, Victor Almanza, Alejandro Bezanilla, Olivier Laurent, Carlos Alberti, Frank Hase, Michel Ramonet, Thomas Lauvaux, Ke Che, and Michel Grutter
EGUsphere, https://doi.org/10.5194/egusphere-2024-512, https://doi.org/10.5194/egusphere-2024-512, 2024
Short summary
Short summary
We studied the variability of CO and CO2 and their ratio over Mexico City from long-term time-resolved FTIR solar absorption and surface measurements. Using the average intraday CO growth rate from total columns and TROPOMI measurements, we additionally estimate the interannual variability of CO and CO2 anthropogenic emissions of the City and relate it to the main influencing events of the last decade, such as the COVID-19 lock-down.
Kai Qin, Wei Hu, Qin He, Fan Lu, and Jason Blake Cohen
Atmos. Chem. Phys., 24, 3009–3028, https://doi.org/10.5194/acp-24-3009-2024, https://doi.org/10.5194/acp-24-3009-2024, 2024
Short summary
Short summary
We compute CH4 emissions and uncertainty on a mine-by-mine basis, including underground, overground, and abandoned mines. Mine-by-mine gas and flux data and 30 min observations from a flux tower located next to a mine shaft are integrated. The observed variability and bias correction are propagated over the emissions dataset, demonstrating that daily observations may not cover the range of variability. Comparisons show both an emissions magnitude and spatial mismatch with current inventories.
Sachin Mishra, Vinayak Sinha, Haseeb Hakkim, Arpit Awasthi, Sachin D. Ghude, Vijay Kumar Soni, Narendra Nigam, Baerbel Sinha, and Madhavan N. Rajeevan
EGUsphere, https://doi.org/10.5194/egusphere-2024-500, https://doi.org/10.5194/egusphere-2024-500, 2024
Short summary
Short summary
We quantified 111 gases using extended volatility mass spectrometry to understand how changes in seasonality and emissions lead from clean air in monsoon to extremely polluted air in the post-monsoon season in Delhi. Averaged total mass concentrations (260 µgm-3) were >4 times in polluted periods, driven by biomass burning emissions and reduced atmospheric ventilation. Reactive gaseous nitrogen, chlorine and sulphur compounds hitherto un-reported from such a polluted environment were discovered.
Theresa Harlass, Rebecca Dischl, Stefan Kaufmann, Raphael Märkl, Daniel Sauer, Monika Scheibe, Paul Stock, Tiziana Bräuer, Andreas Dörnbrack, Anke Roiger, Hans Schlager, Ulrich Schumann, Tobias Schripp, Tobias Grein, Linda Bondorf, Charles Renard, Maxime Gauthier, Mark Johnson, Darren Luff, Paul Madden, Peter Swann, Denise Ahrens, Reetu Sallinen, and Christiane Voigt
EGUsphere, https://doi.org/10.5194/egusphere-2024-454, https://doi.org/10.5194/egusphere-2024-454, 2024
Short summary
Short summary
Emissions from aircraft have a direct impact on our climate. Here, we present airborne and ground based measurement data of nitrogen oxides which were collected in the exhaust of an Airbus aircraft. We study the impact of burning fossil and sustainable aviation fuel on nitrogen oxide emissions at different engine settings related to combustor temperature, pressure and fuel flow. Further, we compare observations with engine emission models.
Yao Yan Huang and D. James Donaldson
Atmos. Chem. Phys., 24, 2387–2398, https://doi.org/10.5194/acp-24-2387-2024, https://doi.org/10.5194/acp-24-2387-2024, 2024
Short summary
Short summary
Ground-level ozone interacts at the lake–land boundary; this is important to our understanding and modelling of atmospheric chemistry and air pollution in the lower atmosphere. We show that a steep ozone gradient occurs year-round moving inland up to 1 km from the lake and that this gradient is influenced by seasonal factors on the local land environment, where more rural areas are more greatly affected seasonally.
Katrin Müller, Jordis S. Tradowsky, Peter von der Gathen, Christoph Ritter, Sharon Patris, Justus Notholt, and Markus Rex
Atmos. Chem. Phys., 24, 2169–2193, https://doi.org/10.5194/acp-24-2169-2024, https://doi.org/10.5194/acp-24-2169-2024, 2024
Short summary
Short summary
The Palau Atmospheric Observatory is introduced as an ideal site to detect changes in atmospheric composition and dynamics above the remote tropical western Pacific. We focus on the ozone sounding program from 2016–2021, including El Niño 2016. The year-round high convective activity is reflected in dominant low tropospheric ozone and high relative humidity. Their seasonal distributions are unique compared to other tropical sites and are modulated by the Intertropical Convergence Zone.
Ziyan Guo, Keding Lu, Pengxiang Qiu, Mingyi Xu, and Zhaobing Guo
Atmos. Chem. Phys., 24, 2195–2205, https://doi.org/10.5194/acp-24-2195-2024, https://doi.org/10.5194/acp-24-2195-2024, 2024
Short summary
Short summary
The formation of secondary sulfate needs to be further explored. In this work, we simultaneously measured sulfur and oxygen isotopic compositions to gain an increased understanding of specific sulfate formation processes. The results indicated that secondary sulfate was mainly ascribed to SO2 homogeneous oxidation by OH radicals and heterogeneous oxidation by H2O2 and Fe3+ / O2. This study is favourable for deeply investigating the sulfur cycle in the atmosphere.
Imran A. Girach, Narendra Ojha, Prabha R. Nair, Kandula V. Subrahmanyam, Neelakantan Koushik, Mohammed M. Nazeer, Nadimpally Kiran Kumar, Surendran Nair Suresh Babu, Jos Lelieveld, and Andrea Pozzer
Atmos. Chem. Phys., 24, 1979–1995, https://doi.org/10.5194/acp-24-1979-2024, https://doi.org/10.5194/acp-24-1979-2024, 2024
Short summary
Short summary
We investigate surface ozone variability in East Antarctica based on measurements and EMAC global model simulations during austral summer. Nearly half of the surface ozone is found to be of stratospheric origin. The east coast of Antarctica acts as a stronger sink of ozone than surrounding regions. Photochemical loss of ozone is counterbalanced by downward transport of ozone. The study highlights the intertwined role of chemistry and dynamics in governing ozone variations over East Antarctica.
Ying Zhang, Duzitian Li, Xu-Cheng He, Wei Nie, Chenjuan Deng, Runlong Cai, Yuliang Liu, Yishuo Guo, Chong Liu, Yiran Li, Liangduo Chen, Yuanyuan Li, Chenjie Hua, Tingyu Liu, Zongcheng Wang, Jiali Xie, Lei Wang, Tuukka Petäjä, Federico Bianchi, Ximeng Qi, Xuguang Chi, Pauli Paasonen, Yongchun Liu, Chao Yan, Jingkun Jiang, Aijun Ding, and Markku Kulmala
Atmos. Chem. Phys., 24, 1873–1893, https://doi.org/10.5194/acp-24-1873-2024, https://doi.org/10.5194/acp-24-1873-2024, 2024
Short summary
Short summary
This study conducts a long-term observation of gaseous iodine oxoacids in two Chinese megacities, revealing their ubiquitous presence with peak concentrations (up to 0.1 pptv) in summer. Our analysis suggests a mix of terrestrial and marine sources for iodine. Additionally, iodic acid is identified as a notable contributor to sub-3 nm particle growth and particle survival probability.
Guoxian Zhang, Renzhi Hu, Pinhua Xie, Changjin Hu, Xiaoyan Liu, Liujun Zhong, Haotian Cai, Bo Zhu, Shiyong Xia, Xiaofeng Huang, Xin Li, and Wenqing Liu
Atmos. Chem. Phys., 24, 1825–1839, https://doi.org/10.5194/acp-24-1825-2024, https://doi.org/10.5194/acp-24-1825-2024, 2024
Short summary
Short summary
Comprehensive observation of HOx radicals was conducted at a coastal site in the Pearl River Delta. Radical chemistry was influenced by different air masses in a time-dependent way. Land mass promotes a more active photochemical process, with daily averages of 7.1 × 106 and 5.2 × 108 cm−3 for OH and HO2 respectively. The rapid oxidation process was accompanied by a higher diurnal HONO concentration, which influences the ozone-sensitive system and eventually magnifies the background ozone.
Sarah Albertin, Joël Savarino, Slimane Bekki, Albane Barbero, Roberto Grilli, Quentin Fournier, Irène Ventrillard, Nicolas Caillon, and Kathy Law
Atmos. Chem. Phys., 24, 1361–1388, https://doi.org/10.5194/acp-24-1361-2024, https://doi.org/10.5194/acp-24-1361-2024, 2024
Short summary
Short summary
This study reports the first simultaneous records of oxygen (Δ17O) and nitrogen (δ15N) isotopes in nitrogen dioxide (NO2) and nitrate (NO3−). These data are combined with atmospheric observations to explore sub-daily N reactive chemistry and quantify N fractionation effects in an Alpine winter city. The results highlight the necessity of using Δ17O and δ15N in both NO2 and NO3− to avoid biased estimations of NOx sources and fates from NO3− isotopic records in urban winter environments.
Shigeyuki Ishidoya, Kazuhiro Tsuboi, Hiroaki Kondo, Kentaro Ishijima, Nobuyuki Aoki, Hidekazu Matsueda, and Kazuyuki Saito
Atmos. Chem. Phys., 24, 1059–1077, https://doi.org/10.5194/acp-24-1059-2024, https://doi.org/10.5194/acp-24-1059-2024, 2024
Short summary
Short summary
A method evaluating techniques for carbon neutrality, such as carbon capture and storage (CCS), is important. This study presents a method to evaluate CO2 emissions from a cement plant based on atmospheric O2 and CO2 measurements. The method will also be useful for evaluating CO2 capture from flue gas at CCS plants, since the plants remove CO2 from the atmosphere without causing any O2 changes, just as cement plants do, differing only in the direction of CO2 exchange with the atmosphere.
Magdalena Pühl, Anke Roiger, Alina Fiehn, Alan M. Gorchov Negron, Eric A. Kort, Stefan Schwietzke, Ignacio Pisso, Amy Foulds, James Lee, James L. France, Anna E. Jones, Dave Lowry, Rebecca E. Fisher, Langwen Huang, Jacob Shaw, Prudence Bateson, Stephen Andrews, Stuart Young, Pamela Dominutti, Tom Lachlan-Cope, Alexandra Weiss, and Grant Allen
Atmos. Chem. Phys., 24, 1005–1024, https://doi.org/10.5194/acp-24-1005-2024, https://doi.org/10.5194/acp-24-1005-2024, 2024
Short summary
Short summary
In April–May 2019 we carried out an airborne field campaign in the southern North Sea with the aim of studying methane emissions of offshore gas installations. We determined methane emissions from elevated methane measured downstream of the sampled installations. We compare our measured methane emissions with estimated methane emissions from national and global annual inventories. As a result, we find inconsistencies of inventories and large discrepancies between measurements and inventories.
Simone T. Andersen, Max R. McGillen, Chaoyang Xue, Tobias Seubert, Patrick Dewald, Gunther N. T. E. Türk, Jan Schuladen, Cyrielle Denjean, Jean-Claude Etienne, Olivier Garrouste, Marina Jamar, Sergio Harb, Manuela Cirtog, Vincent Michoud, Mathieu Cazaunau, Antonin Bergé, Christopher Cantrell, Sebastien Dusanter, Bénédicte Picquet-Varrault, Alexandre Kukui, Abdelwahid Mellouki, Lucy J. Carpenter, Jos Lelieveld, and John N. Crowley
EGUsphere, https://doi.org/10.5194/egusphere-2023-2848, https://doi.org/10.5194/egusphere-2023-2848, 2024
Short summary
Short summary
Through measurements of various trace gases in a sub-urban forest near Paris in the summer of 2022 we were able to gain insight into the sources and sinks of NOx (NO+NO2) with a special focus on their nighttime chemical/physical loss processes. NO was observed as a result of nighttime soil emissions when ozone levels were strongly depleted by deposition. NO oxidation products were not observed at night indicating that soil and/or foliar surfaces are an efficient sink of reactive nitrogen.
Georgios I. Gkatzelis, Matthew M. Coggon, Chelsea E. Stockwell, Rebecca S. Hornbrook, Hannah Allen, Eric C. Apel, Megan M. Bela, Donald R. Blake, Ilann Bourgeois, Steven S. Brown, Pedro Campuzano-Jost, Jason M. St. Clair, James H. Crawford, John D. Crounse, Douglas A. Day, Joshua P. DiGangi, Glenn S. Diskin, Alan Fried, Jessica B. Gilman, Hongyu Guo, Johnathan W. Hair, Hannah S. Halliday, Thomas F. Hanisco, Reem Hannun, Alan Hills, L. Gregory Huey, Jose L. Jimenez, Joseph M. Katich, Aaron Lamplugh, Young Ro Lee, Jin Liao, Jakob Lindaas, Stuart A. McKeen, Tomas Mikoviny, Benjamin A. Nault, J. Andrew Neuman, John B. Nowak, Demetrios Pagonis, Jeff Peischl, Anne E. Perring, Felix Piel, Pamela S. Rickly, Michael A. Robinson, Andrew W. Rollins, Thomas B. Ryerson, Melinda K. Schueneman, Rebecca H. Schwantes, Joshua P. Schwarz, Kanako Sekimoto, Vanessa Selimovic, Taylor Shingler, David J. Tanner, Laura Tomsche, Krystal T. Vasquez, Patrick R. Veres, Rebecca Washenfelder, Petter Weibring, Paul O. Wennberg, Armin Wisthaler, Glenn M. Wolfe, Caroline C. Womack, Lu Xu, Katherine Ball, Robert J. Yokelson, and Carsten Warneke
Atmos. Chem. Phys., 24, 929–956, https://doi.org/10.5194/acp-24-929-2024, https://doi.org/10.5194/acp-24-929-2024, 2024
Short summary
Short summary
This study reports emissions of gases and particles from wildfires. These emissions are related to chemical proxies that can be measured by satellite and incorporated into models to improve predictions of wildfire impacts on air quality and climate.
Jie Wang, Haichao Wang, Yee Jun Tham, Lili Ming, Zelong Zheng, Guizhen Fang, Cuizhi Sun, Zhenhao Ling, Jun Zhao, and Shaojia Fan
Atmos. Chem. Phys., 24, 977–992, https://doi.org/10.5194/acp-24-977-2024, https://doi.org/10.5194/acp-24-977-2024, 2024
Short summary
Short summary
Many works report NO3 chemistry in inland regions while less target marine regions. We measured N2O5 and related species on a typical island and found intensive nighttime chemistry and rapid NO3 loss. NO contributed significantly to NO3 loss despite its sub-ppbv level, suggesting nocturnal NO3 reactions would be largely enhanced once free from NO emissions in the open ocean. This highlights the strong influences of urban outflow on downward marine areas in terms of nighttime chemistry.
Tanja J. Schuck, Johannes Degen, Eric Hintsa, Peter Hoor, Markus Jesswein, Timo Keber, Daniel Kunkel, Fred Moore, Florian Obersteiner, Matt Rigby, Thomas Wagenhäuser, Luke M. Western, Andreas Zahn, and Andreas Engel
Atmos. Chem. Phys., 24, 689–705, https://doi.org/10.5194/acp-24-689-2024, https://doi.org/10.5194/acp-24-689-2024, 2024
Short summary
Short summary
We study the interhemispheric gradient of sulfur hexafluoride (SF6), a strong long-lived greenhouse gas. Its emissions are stronger in the Northern Hemisphere; therefore, mixing ratios in the Southern Hemisphere lag behind. Comparing the observations to a box model, the model predicts air in the Southern Hemisphere to be older. For a better agreement, the emissions used as model input need to be increased (and their spatial pattern changed), and we need to modify north–south transport.
Jérémy Gueffier, François Gheusi, Marie Lothon, Véronique Pont, Alban Philibert, Fabienne Lohou, Solène Derrien, Yannick Bezombes, Gilles Athier, Yves Meyerfeld, Antoine Vial, and Emmanuel Leclerc
Atmos. Chem. Phys., 24, 287–316, https://doi.org/10.5194/acp-24-287-2024, https://doi.org/10.5194/acp-24-287-2024, 2024
Short summary
Short summary
This study investigates the link between weather regime and atmospheric composition at a Pyrenean observatory. Five years of meteorological data were synchronized on a daily basis and then, using a clustering method, separated into six groups of observation days, with most showing marked characteristics of different weather regimes (fair and disturbed weather, winter windstorms, foehn). Statistical differences in gas and particle concentrations appeared between the groups and are discussed.
Nathaniel Brockway, Peter K. Peterson, Katja Bigge, Kristian D. Hajny, Paul B. Shepson, Kerri A. Pratt, Jose D. Fuentes, Tim Starn, Robert Kaeser, Brian H. Stirm, and William R. Simpson
Atmos. Chem. Phys., 24, 23–40, https://doi.org/10.5194/acp-24-23-2024, https://doi.org/10.5194/acp-24-23-2024, 2024
Short summary
Short summary
Bromine monoxide (BrO) strongly affects atmospheric chemistry in the springtime Arctic, yet there are still many uncertainties around its sources and recycling, particularly in the context of a rapidly changing Arctic. In this study, we observed BrO as a function of altitude above the Alaskan Arctic. We found that BrO was often most concentrated near the ground, confirming the ability of snow to produce and recycle reactive bromine, and identified four common vertical distributions of BrO.
Cited articles
Aspmo, K., Temme, C., Berg, T., Ferrari, C., Gauchard, P. A., Fain, X., and Wibetoe, G.: Mercury in the atmosphere, snow and melt water ponds in the North Atlantic Ocean during Arctic summer, Environ. Sci. Technol., 40, 4083–4089, 2006.
Carpi, A. and Lindberg, S. E.: Sunlight-mediated emission of elemental mercury from soil amended with municipal sewage sludge, Environ. Sci. Technol., 31, 2085–2091, 1997.
Carpi, A. and Lindberg, S. E.: Application of a Teflon dynamic flux chamber for quantifying soil mercury flux: Test and results over background soil, Atmos. Environ., 32, 873–882, 1998.
Ci, Z., Zhang, X., Wang, Z., and Niu, Z.: Atmospheric gaseous elemental mercury (GEM) over a coastal/rural site downwind of East China Temporal variation and long-range transport, Atmos. Environ., 45, 2480–2487, 2011.
Engle, M. A., Tate, M. T., Krabbenhoft, D. P., Kolker, A., Olson, M. L., Edgerton, E. S., DeWild, J. F., and McPherson, A. K.: Characterization and cycling of atmospheric mercury along the central US Gulf Coast, Appl. Geochem., 23, 419–437, 2008.
Fang, F. M., Wang, Q. C., and Li, J. F.: Urban environmental mercury in Changchun, a metropolitan city in Northeastern China source, cycle, and fate, Sci. Total Environ., 330, 159–170, 2004.
Feng, X., Shang, L., Wang, S., Tang, S., and Zheng, W.: Temporal variation of total gaseous mercury in the air of Guiyang, China, J. Geophys. Res., 109, D03303, https://doi.org/10.1029/2003JD004159, 2004.
Feng, X., Tang, S., Shang, L., Yan, H., Sommar, J., and Lindqvist, O.: Total gaseous mercury in the atmosphere of Guiyang, PR China, Sci. Total Environ., 304, 61–72, 2003.
Fitzgerald, W. F., Engstrom, D. R., Mason, and R. P., Nater, E. A.: The case for atmospheric mercury contamination in remote areas, Environ. Sci. Technol. 32, 1–7, 1998.
Friedli, H. R., Arellano Jr., A. F., Geng, F., Cai, C., and Pan, L.: Measurements of atmospheric mercury in Shanghai during September 2009, Atmos. Chem. Phys., 11, 3781–3788, https://doi.org/10.5194/acp-11-3781-2011, 2011.
Fu, X. W., Feng, X., Dong, Z. Q., Yin, R. S., Wang, J. X., Yang, Z. R., and Zhang, H.: Atmospheric gaseous elemental mercury (GEM) concentrations and mercury depositions at a high-altitude mountain peak in south China, Atmos. Chem. Phys., 10, 2425–2437, https://doi.org/10.5194/acp-10-2425-2010, 2010.
Fu, X., Feng, X., Wang, S., Rothenberg, S., Shang, L., Li, Z. and Qiu, G.: Temporal and spatial distributions of total gaseous mercury concentrations in ambient air in a mountainous area in southwestern China implications for industrial and domestic mercury emissions in remote areas in China, Sci. Total Environ., 407, 2306–2314, 2009.
Fu, X. W., Feng, X. B., Zhu, W. Z., Wang, S. F., and Lu, J.: Total gaseous mercury concentrations in ambient air in the eastern slope of Mt. Gongga, South-Eastern fringe of the Tibetan plateau, China. Atmos. Environ., 42, 970–979, 2008a.
Fu, X. W., Feng, X. B., Zhu, W. Z., Zheng, W., Wang, S. F., and Lu, J.: Total particulate and reactive gaseous mercury in ambient air on the eastern slope of the Mt. Gongga area. China. Appl. Geochem. 23, 408–418, 2008b.
Fu, X. W., Feng, X., Shang, L. H., Wang, S. F., and Zhang, H.: Two years of measurements of atmospheric total gaseous mercury (TGM) at a remote site in Mt. Changbai area, Northeastern China, Atmos. Chem. Phys., 12, 4215–4226, https://doi.org/10.5194/acp-12-4215-2012, 2012.
Gabriel, M. C., Williamson, D. G., Brooks, S., and Lindberg, S.: Atmospheric speciation of mercury in two contrasting Southeastern US airsheds, Atmos. Environ., 39, 4947–4958, 2005.
Gustin, M. S. and Lindberg, S. E.: Assessing the contribution of natural sources to the global mercury cycle: The importance of intercomparing dynamic flux measurements, Fresenius J. Anal. Chem., 266, 417–442, 2000.
Gustin, M. S., Biester, H., and Kim, C. S.: Investigation of the light enhanced emission of mercury from naturally enriched substrates, Atmos. Environ., 36, 3241– 3254, 2002.
Gustin, M. S., Rasmussen, P., Edwards, G., Schroeder, W., and Kemp, J.: Application of a laboratory gas exchange chamber for assessment of in situ mercury emissions, J. Geophys. Res., 104, 873–878, 1999.
Huang, C., Chen, C. H., Li, L., Cheng, Z., Wang, H. L., Huang, H. Y., Streets, D. G., Wang, Y. J., Zhang, G. F., and Chen, Y. R.: Emission inventory of anthropogenic air pollutants and VOC species in the Yangtze River Delta region, China, Atmos. Chem. Phys.,11, 4105–4120, https://doi.org/10.5194/acp-11-4105-2011, 2011.
Jensen, A. and Iverfeldt, A.: Atmospheric bulk deposition of mercury to the southern Baltic sea area, in Mercury Pollution: Integration and Synthesis, edited by: Watras, C. J. and Huckabee, J. W., 221–229, Lewis, A. F., New York, 1994.
Kellerhals, M., Beauchamp, S., Belzer, W., Blanchard, P., Froude, F., Harvey, B., McDonald, K., Pilote, M., Poissant, L., Puckett, K., Schroeder, B., Steffen, A., and Tordon, R.: Temporal and spatial variability of total gaseous mercury in Canada: results from the Canadian Atmospheric Mercury Measurement Network (CAMNet), Atmos. Environ., 37, 1003–1011, 2003.
Kim, K. H. and Kim, M. Y.: The temporal distribution characteristics of total gaseous mercury at an urban monitoring site in Seoul during 1999–2000, Atmos. Environ., 35, 4253–4263, 2001.
Kim, S. Y.: Continental outflow of polluted air from the U.S. to the North Atlantic and mercury cycling in various 5 Atmospheric environments, Ph.D. dissertation, 114 pp., University of New Hampshire, September 2010.
Kock, H. H., Bieber, E., Ebinghaus, R., Spain, T. G., and Thees, B.: Comparison of long-term trends and seasonal variations of atmospheric mercury concentrations at the two European coastal monitoring stations Mace Head, Ireland, and Zingst, Germany, Atmos. Environ., 39, 7549–7556, 2005.
Kuo, T.H., Chang, C.F., Urba, A., and Kvietkus, K.: Atmospheric gaseous mercury in Northern Taiwan, Sci. Total Environ., 368, 10–18, 2006.
Lee, D. S., Dollard, G. J., and Pepler, S.: Gas-phase mercury in the atmosphere of the United Kingdom, Atmos. Environ., 32, 855–864, 1998.
Leonard, T. L., Taylor, G. E., Gustin, M. S., and Fernandez, G. C. J.: Mercury and plants in contaminated soils: 1. Uptake, partitioning, and emission to the atmosphere, Environ. Toxicol. Chem., 17, 2063–2071, 1998.
Li, J., Yang, Y., Xiao, G., and Wei, S.: Sourcing Contributions of Gaseous Mercury in Indoor and Outdoor Air in China, Environ. Forens., 11, 154–160, 2010
Li, Z., Xia., C., Wang, X., Xiang, Y., and Xie, Z.: Total gaseous mercury in Pearl River Delta region, China during 2008 winter period, Atmos. Environ., 45, 834–838, 2011.
Lindberg, S. E., Meyers, T. P., Taylor, G. E., Turner, R. R., and Schroeder, W. H.: Atmospheric/surface exchange of mercury in a forest: results of modeling and gradient approaches, J. Geophys. Res., 97, 2519–2528, 1992.
Lindqvist, O.: Mercury in the Swedish environment: recent research on causes, consequences and corrective methods, Water Air Soil Pollut., 55, 1–261, 1991.
Liu, B., Keeler, G. J., Dvonch, J. T., Barres, J. A., Lynam, M. M., Marsik, F. J., and Morgan, J. T.: Temporal variability of mercury speciation in urban air. Atmos. Environ., 41, 1911–1923, 2007.
Liu, N., Qiu, G. l., Landis, M. S., Feng, X., Fu, X., and Shang, L.: Atmospheric mercury species measured in Guiyang, Guizhou province, southwest China, Atmos. Res., 100, 93–102, 2011.
Liu, S., Nadim, F., Perkins, C., Carley, R. J., Hoag, G. E., Lin, Y. H., and Chen, L. T.: Atmospheric mercury monitoring survey in Beijing, China, Chemos., 48, 97–107, 2002.
Mao, H. and Talbot, R.: O3 and CO in New England: Temporal variations and relationships, J. Geophys. Res., 109, D21304,https://doi.org/10.1029/2004JD004913, 2004.
Mao, H., Talbot, R. W., Sigler, J. M., Sive, B. C., and Hegarty, J. D.: Seasonal and diurnal variations of Hgo over New England. Atmos. Chem. Phys., 8, 1403–1421, 2008.
Mao, H., Talbot, R., Hegarty, J., and Koermer, J.: Speciated mercury at marine, coastal, and inland sites in New England – Part 2: Relationships with atmospheric physical parameters, Atmos. Chem. Phys., 12, 4181–4206, https://doi.org/10.5194/acp-12-4181-2012, 2012.
Mason, R. P., Fitzgerald, W. F., and Morel, F. M.: The biogeochemical cycling of elemental mercury: anthropogenic influences, Geochim. Cosmochim. Acta, 58, 3191–3198, 1994.
Pacyna, E. G., Pacyna, J. M., Steenhuisen, F., and Wilson, S.: Global anthropogenic mercury emission inventory for 2000. Atmos. Environ. 40, 4048-4063, 2006.
Pacyna, E. G., Pacyna, J. M., Sundseth, K., Munthe, J., Kindbom, K., Wilson, S., Steenhuisen, F., and Maxson, P.: Global emission of mercury to the atmosphere from anthropogenic sources in 2005 and projections to 2020, Atmos. Environ., 44, 2487–2499, 2010.
Peterson, C., Gustin, M., and Lyman, S.: Atmospheric mercury concentrations and speciation measured from 2004 to 2007 in Reno, Nevada, USA, Atmos. Environ., 43, 4646–4654, 2009.
Poissant, L. and Casimir, A.: Water–air and soil-air exchange rate of total gaseous mercury measured at background sites, Atmos. Environ., 32, 883–893, 1998.
Poissant, L., Pilote, M., Beauvais, C., Constant, P., and Zhang, H. H.: A year of continuous measurements of three atmospheric mercury species (GEM, RGM and Hg-P) in southern Quebec, Canada, Atmos. Environ., 39, 1275–1287, 2005.
Quan, J., Zhang, X., and Shim, S.: Estimation of vegetative mercury emissions in China, 20, 1070–1074, 2008.
Schmolke, S. R., Schroeder, W. H., Kock, H. H., Schneeberger, D., Munthe, J., and Ebinghaus, R.: Simultaneous measurements of total gaseous mercury at four sites on a 800 km transect: spatial distribution and short-time variability of total gaseous mercury over central Europe. Atmos. Environ., 33, 1725–1733, 1999.
Scholtz, M. T., Van Heyst, B. J., and Schroeder, W. H.: Modelling of mercury emissions from background soils, Sci. Total Environ., 304, 185–207, 2003.
Schroeder, W. H. and Munthe, J.: Atmospheric mercury – an overview, Atmos. Environ., 32, 809–822, 1998.
Shetty, S., Lin, C., Streets, D., and Jang, C.: Model estimate of mercury emission from natural sources in East Asia, 42, 8674–8685, 2008.
Sigler, J. M., Mao, H., and Talbot, R.: Gaseous elemental and reactive mercury in Southern New Hampshire, Atmos. Chem. Phys., 9, 1929–1942, https://doi.org/10.5194/acp-9-1929-2009, 2009.
Slemr, F., Brunke, E. G., Ebinghaus, R., Temme, C., Munthe, J., Wangberg, I., Schroeder, W., Steffen, A., and Berg, T.: Worldwide trend of atmospheric mercury since 1977, Geophys. Res. Lett., 30, 1516–1520, 2003.
Slemr, F., Schuster, G., and Seiler, W.: Distribution, speciation, and budget of atmospheric mercury, J. Atmos. Chem., 3, 407–434, 1985.
Song, X., Cheng, I., and Lu, J.: Annual atmospheric mercury species in Downtown Toronto, Canada, J. Environ. Monit., 11, 660–669, 2009.
Sprovieri, F., Pirrone, N., and Sommar, J.: Mercury speciation in the marine boundary layer along a 6000 km cruise path around the Mediterranean Sea. Atmos. Environ., 37, suppl. 1, 63–71, 2003.
Sprovieri, F., Pirrone, N., Ebinghaus, R., Kock, H., and Dommergue, A.: A review of worldwide atmospheric mercury measurements, Atmos. Chem. Phys., 10, 8245–8265, https://doi.org/10.5194/acp-10-8245-2010, 2010.
Stamenkovic, J., Lyman, S., and Gustin, M. S.: Seasonal and diel variation of atmospheric mercury concentrations in the Reno (Nevada, USA) airshed, Atmos. Environ., 41, 6662–6672, 2007.
Street, D. G., Hao, J. M., Wu, Y., Jiang, J. K., Chan, M., and Tian, H. Z.: Anthropogenic mercury emission in China, Atmos. Environ., 39, 7789–7806, 2005.
Temme, C., Slemr, F., Ebinghaus, R., and Einax, J. W.: Distribution of mercury over the Atlantic Ocean in 1996 and 1999–2001, Atmos. Environ. 37, 1889–1897, 2003.
Valente, R. J., Shea, C., Humes, K. L., and Tanner, R. L.: Atmospheric mercury in the Great Smoky Mountains compared to regional and global levels, Atmos. Environ., 41, 1861–1873, 2007.
Valente, R. J., Shea, C., Humes, K. L., and Tanner, R. L.: Atmospheric mercury in the Great Smoky Mountains compared to regional and global levels, Atmos. Environ., 41, 1861–1873, 2007.
Wallschlager, D., Turner, R. R., London, J., Ebinghaus, R., Kock, H. H., Sommar, J., and Xiao, J.: Factors affecting the measurement of mercury emissions from soils with flux chambers, J. Geophys. Res., 104, 859–871,1999.
Wan, Q., Feng, X. B., Lu, J. L., Zheng, W., Song, X. J., Li, P., Han, S. J., and Xu, H.: Atmospheric mercury in Changbai Mountain area, northeastern China I: the season distribution pattern of total gaseous mercury and its potential sources, Environ. Res. 109, 201–206, 2009.
Wang, Z. W., Chen, Z. S., Duan, N., and Zhang, X. S.: Gaseous elemental mercury concentration in atmosphere at urban and remote sites in China, J. Environ. Sci., 19, 176–180, 2007.
Wangberg, I., Munthe, J., Berg, T., Ebinghaus, R., Kock, H. H., Temme, C., Bieber, E., et al.: Trends in air concentration and deposition of mercury in the coastal environment of the North Sea Area, Atmos. Environ., 41, 2612–2619, 2007.
Warneck, P.: Chemistry of the Natural Atmosphere, Academic, San Diego, CA, USA, 340 pp., 1988.
Weiss-Penzias, P., Jaffe, D. A. Swartzendruber, P. Hafner, W. Chand, D., and Prestbo, E.: Quantifying Asian and biomass burning sources of mercury using the Hg/CO ratio in pollution plumes observed at the Mt. Bachelor Observatory, Atmos. Environ., 41, 4366–4379, 2007.
Wu, Y., Wang, S., Streets, D. G., Hao., J., Chan, M. and Jiang, J.: Trends in Anthropogenic Mercury Emissions in China from 1995 to 2003, Environ. Sci. Technol., 40, 5312–5318, 2006.
Wu, Y., Wang, S., Streets, D. G., Hao, J., Chan, M., and Jiang, J.: Trends in anthropogenic mercury emissions in China from 1995 to 2003, Environ. Sci. Technol., 40, 5312–5318, 2006.
Xia, C. H., Xie, Z. Q., Sun, and L. G.: Atmospheric mercury in the marine boundary layer along a cruise path from Shanghai, China to Prydz Bay, Antarctica, Atmos. Environ., 44, 1815–1821, 2010.
Yang, Y., Chen, H., and Wang, D.: Spatial and temporal distribution of gaseous elemental mercury in Chongqing, China, Environ. Monit. Assess., 156, 479–489, 2009.
Zhang, H., Lindberg, S. E., Marsik, F. J. and Keeler, G. J.: Mercury air/surface exchange kinetics of background soils of the Tahquamenon River Watershed in the Michigan Upper Penninsula, Water Air Soil Pollut., 126, 151–169, 2001.
Zheng, W., Feng, X. B., and Yan, H. Y.: Characteristics of total particulate mercury pollution in the atmosphere of a residential area in the city of Guiyang, PR China, Earth Environ., 35, 154–157, 2007.
Altmetrics
Final-revised paper
Preprint