Articles | Volume 15, issue 14
https://doi.org/10.5194/acp-15-7877-2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
https://doi.org/10.5194/acp-15-7877-2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Review article
| 
17 Jul 2015
Review article |
| 17 Jul 2015
Overview of receptor-based source apportionment studies for speciated atmospheric mercury
I. Cheng
Air Quality Research Division, Science and Technology Branch, Environment Canada, 4905 Dufferin Street, Toronto, Ontario, M3H 5T4, Canada
X. Xu
Department of Civil and Environmental Engineering, University of Windsor, 401 Sunset Avenue, Windsor, Ontario, N9B 3P4, Canada
Air Quality Research Division, Science and Technology Branch, Environment Canada, 4905 Dufferin Street, Toronto, Ontario, M3H 5T4, Canada
Related authors
Irene Cheng, Amanda Cole, Leiming Zhang, and Alexandra Steffen
EGUsphere, https://doi.org/10.5194/egusphere-2024-2895, https://doi.org/10.5194/egusphere-2024-2895, 2024
Short summary
Short summary
Using the Positive Matrix Factorization (PMF) model and observations, we showed natural surface emission (wildfires and re-emitted Hg) dominated anthropogenic contributions to total gaseous mercury (TGM). Decreasing TGM was due to reduced shipping and regional emissions. This has led to increasing relative contributions from natural surface emissions of 1.0–1.6 % yr-1. Results showed Hg control measures have been effective, but greater attention is needed on monitoring surface re-emissions.
Irene Cheng, Leiming Zhang, Zhuanshi He, Hazel Cathcart, Daniel Houle, Amanda Cole, Jian Feng, Jason O'Brien, Anne Marie Macdonald, Julian Aherne, and Jeffrey Brook
Atmos. Chem. Phys., 22, 14631–14656, https://doi.org/10.5194/acp-22-14631-2022, https://doi.org/10.5194/acp-22-14631-2022, 2022
Short summary
Short summary
Nitrogen (N) and sulfur (S) deposition decreased significantly at 14 Canadian sites during 2000–2018. The greatest decline was observed in southeastern Canada owing to regional SO2 and NOx reductions. Wet deposition was more important than dry deposition, comprising 71–95 % of total N and 45–89 % of total S deposition. While critical loads (CLs) were exceeded at a few sites in the early 2000s, acidic deposition declined below CLs after 2012, which signifies recovery from legacy acidification.
Xin Qiu, Irene Cheng, Fuquan Yang, Erin Horb, Leiming Zhang, and Tom Harner
Atmos. Chem. Phys., 18, 3457–3467, https://doi.org/10.5194/acp-18-3457-2018, https://doi.org/10.5194/acp-18-3457-2018, 2018
Short summary
Short summary
We developed emissions databases for polycyclic aromatic compounds (PACs) in the Athabasca oil sands region and evaluated the emissions databases by comparing CALPUFF-modelled concentrations with monitored data. Model–measurement agreement improved near oil sands mines due to updated PAC emissions from tailings ponds. Modelled concentrations were underestimated at remote sites and for alkylated PACs suggesting that the emissions of PACs particularly alkylated compounds are underestimated.
Irene Cheng and Leiming Zhang
Atmos. Chem. Phys., 17, 4711–4730, https://doi.org/10.5194/acp-17-4711-2017, https://doi.org/10.5194/acp-17-4711-2017, 2017
Short summary
Short summary
Geographical and long-term (1983–2011) trends in air concentrations and wet deposition of inorganic ions and aerosol and precipitation acidity were analyzed at 31 sites in Canada. Declines in atmospheric ammonium, nitrate, and sulfate were consistent with decreasing emissions of NH3, NOx, and SO2. A decline in nitrate and sulfate wet deposition was also observed. Wet scavenging was further studied by estimating scavenging ratios and relative contributions of gases and aerosols to wet deposition.
Xiaohong Xu, Yanyin Liao, Irene Cheng, and Leiming Zhang
Atmos. Chem. Phys., 17, 1381–1400, https://doi.org/10.5194/acp-17-1381-2017, https://doi.org/10.5194/acp-17-1381-2017, 2017
Short summary
Short summary
This study addresses two issues related to source–receptor analysis of speciated atmospheric mercury: (1) comparing PMF and PCA and (2) testing different approaches in data selection for PMF modeling.
Huiting Mao, Irene Cheng, and Leiming Zhang
Atmos. Chem. Phys., 16, 12897–12924, https://doi.org/10.5194/acp-16-12897-2016, https://doi.org/10.5194/acp-16-12897-2016, 2016
Short summary
Short summary
Understanding of spatial and temporal variations of atmospheric speciated mercury can advance our knowledge of mercury cycling in various environments. This review summarized spatiotemporal variations of TGM/GEM, GOM, and PBM in environments including oceans, continents, high elevation, the free troposphere, and low to high latitudes. Remaining questions/issues and recommendations were provided for future research.
L. Zhang, I. Cheng, D. Muir, and J.-P. Charland
Atmos. Chem. Phys., 15, 1421–1434, https://doi.org/10.5194/acp-15-1421-2015, https://doi.org/10.5194/acp-15-1421-2015, 2015
Short summary
Short summary
This study analyzed air and precipitation concentrations of 43 polycyclic aromatic compounds (PACs) collected in the Athabasca oil sands region. A database has been built for the parameter scavenging ratio, which is defined as the ratio of the concentration of PACs in precipitation to that in air. A better understanding of the potential differences between gas and particulate scavenging and between snow and rain scavenging has been achieved.
Tamara Emmerichs, Abdulla Al Mamun, Lisa Emberson, Huiting Mao, Leiming Zhang, Limei Ran, Clara Betancourt, Anthony Wong, Gerbrand Koren, Giacomo Gerosa, Min Huang, and Pierluigi Guaita
EGUsphere, https://doi.org/10.5194/egusphere-2025-429, https://doi.org/10.5194/egusphere-2025-429, 2025
This preprint is open for discussion and under review for Biogeosciences (BG).
Short summary
Short summary
The risk of ozone pollution to plants is estimated based on the flux through the plant pores which still has uncertainties. In this study, we estimate this quantity with 9 models at different land types worldwide. The input data stems from a database. The models estimated mostly reasonable summertime ozone deposition. The different results of the models varied by land cover which were mostly related to the moisture deficit. This is an important step for assessing the ozone impact on vegetation.
Zihan Song, Leiming Zhang, Chongguo Tian, Qiang Fu, Zhenxing Shen, Renjian Zhang, Dong Liu, and Song Cui
Atmos. Chem. Phys., 24, 13101–13113, https://doi.org/10.5194/acp-24-13101-2024, https://doi.org/10.5194/acp-24-13101-2024, 2024
Short summary
Short summary
A novel concept integrating crop cycle information into fire spot extraction was proposed. Spatiotemporal variations of open straw burning in Northeast China are revealed. Open straw burning in Northeast China emitted a total of 218 Tg of CO2-eq during 2001–2020. The policy of banning straw burning effectively reduced greenhouse gas emissions.
Anam M. Khan, Olivia E. Clifton, Jesse O. Bash, Sam Bland, Nathan Booth, Philip Cheung, Lisa Emberson, Johannes Flemming, Erick Fredj, Stefano Galmarini, Laurens Ganzeveld, Orestis Gazetas, Ignacio Goded, Christian Hogrefe, Christopher D. Holmes, Laszlo Horvath, Vincent Huijnen, Qian Li, Paul A. Makar, Ivan Mammarella, Giovanni Manca, J. William Munger, Juan L. Perez-Camanyo, Jonathan Pleim, Limei Ran, Roberto San Jose, Donna Schwede, Sam J. Silva, Ralf Staebler, Shihan Sun, Amos P. K. Tai, Eran Tas, Timo Vesala, Tamas Weidinger, Zhiyong Wu, Leiming Zhang, and Paul C. Stoy
EGUsphere, https://doi.org/10.5194/egusphere-2024-3038, https://doi.org/10.5194/egusphere-2024-3038, 2024
Short summary
Short summary
Vegetation removes tropospheric ozone through stomatal uptake, and accurately modeling the stomatal uptake of ozone is important for modeling dry deposition and air quality. We evaluated the stomatal component of ozone dry deposition modeled by atmospheric chemistry models at six sites. We find that models and observation-based estimates agree at times during the growing season at all sites, but some models overestimated the stomatal component during the dry summers at a seasonally dry site.
Irene Cheng, Amanda Cole, Leiming Zhang, and Alexandra Steffen
EGUsphere, https://doi.org/10.5194/egusphere-2024-2895, https://doi.org/10.5194/egusphere-2024-2895, 2024
Short summary
Short summary
Using the Positive Matrix Factorization (PMF) model and observations, we showed natural surface emission (wildfires and re-emitted Hg) dominated anthropogenic contributions to total gaseous mercury (TGM). Decreasing TGM was due to reduced shipping and regional emissions. This has led to increasing relative contributions from natural surface emissions of 1.0–1.6 % yr-1. Results showed Hg control measures have been effective, but greater attention is needed on monitoring surface re-emissions.
Pierluigi Renan Guaita, Riccardo Marzuoli, Leiming Zhang, Steven Turnock, Gerbrand Koren, Oliver Wild, Paola Crippa, and Giacomo Alessandro Gerosa
EGUsphere, https://doi.org/10.5194/egusphere-2024-2573, https://doi.org/10.5194/egusphere-2024-2573, 2024
Preprint archived
Short summary
Short summary
This study assesses the global impact of tropospheric ozone on wheat crops in the 21st century under various climate scenarios. The research highlights that ozone damage to wheat varies by region and depends on both ozone levels and climate. Vulnerable regions include East Asia, Northern Europe, and the Southern and Eastern edges of the Tibetan Plateau. Our results emphasize the need of policies to reduce ozone levels and mitigate climate change to protect global food security.
Xiaohong Yao and Leiming Zhang
Atmos. Chem. Phys., 24, 7773–7791, https://doi.org/10.5194/acp-24-7773-2024, https://doi.org/10.5194/acp-24-7773-2024, 2024
Short summary
Short summary
This study investigates long-term trends of criteria air pollutants, including NO2, CO, SO2, O3 and PM2.5, and NO2+O3 measured in 10 Canadian cities during the last 2 to 3 decades. We also investigate associated driving forces in terms of emission reductions, perturbations from varying weather conditions and large-scale wildfires, as well as changes in O3 sources and sinks.
Juanjuan Qin, Leiming Zhang, Yuanyuan Qin, Shaoxuan Shi, Jingnan Li, Zhao Shu, Yuwei Gao, Ting Qi, Jihua Tan, and Xinming Wang
Atmos. Chem. Phys., 24, 7575–7589, https://doi.org/10.5194/acp-24-7575-2024, https://doi.org/10.5194/acp-24-7575-2024, 2024
Short summary
Short summary
The present research unveiled that acidity dominates while transition metal ions harmonize with the light absorption properties of humic-like substances (HULIS). Cu2+ has quenching effects on HULIS by complexation, hydrogen substitution, or electrostatic adsorption, with aromatic structures of HULIS. Such effects are less pronounced if from Mn2+, Ni2+, Zn2+, and Cu2+. Oxidized HULIS might contain electron-donating groups, whereas N-containing compounds might contain electron-withdrawing groups.
Olivia E. Clifton, Donna Schwede, Christian Hogrefe, Jesse O. Bash, Sam Bland, Philip Cheung, Mhairi Coyle, Lisa Emberson, Johannes Flemming, Erick Fredj, Stefano Galmarini, Laurens Ganzeveld, Orestis Gazetas, Ignacio Goded, Christopher D. Holmes, László Horváth, Vincent Huijnen, Qian Li, Paul A. Makar, Ivan Mammarella, Giovanni Manca, J. William Munger, Juan L. Pérez-Camanyo, Jonathan Pleim, Limei Ran, Roberto San Jose, Sam J. Silva, Ralf Staebler, Shihan Sun, Amos P. K. Tai, Eran Tas, Timo Vesala, Tamás Weidinger, Zhiyong Wu, and Leiming Zhang
Atmos. Chem. Phys., 23, 9911–9961, https://doi.org/10.5194/acp-23-9911-2023, https://doi.org/10.5194/acp-23-9911-2023, 2023
Short summary
Short summary
A primary sink of air pollutants is dry deposition. Dry deposition estimates differ across the models used to simulate atmospheric chemistry. Here, we introduce an effort to examine dry deposition schemes from atmospheric chemistry models. We provide our approach’s rationale, document the schemes, and describe datasets used to drive and evaluate the schemes. We also launch the analysis of results by evaluating against observations and identifying the processes leading to model–model differences.
Yu Lin, Leiming Zhang, Qinchu Fan, He Meng, Yang Gao, Huiwang Gao, and Xiaohong Yao
Atmos. Chem. Phys., 22, 16073–16090, https://doi.org/10.5194/acp-22-16073-2022, https://doi.org/10.5194/acp-22-16073-2022, 2022
Short summary
Short summary
In this study, we analyzed 7-year (from May 2014 to April 2021) concentration data of six criteria air pollutants (PM2.5, PM10, O3, NO2, CO and SO2) as well as the sum of NO2 and O3 in six cities in South China. Three different analysis methods were used to identify emission-driven interannual variations and perturbations from varying weather conditions. In addition, a self-developed method was further introduced to constrain analysis uncertainties.
Irene Cheng, Leiming Zhang, Zhuanshi He, Hazel Cathcart, Daniel Houle, Amanda Cole, Jian Feng, Jason O'Brien, Anne Marie Macdonald, Julian Aherne, and Jeffrey Brook
Atmos. Chem. Phys., 22, 14631–14656, https://doi.org/10.5194/acp-22-14631-2022, https://doi.org/10.5194/acp-22-14631-2022, 2022
Short summary
Short summary
Nitrogen (N) and sulfur (S) deposition decreased significantly at 14 Canadian sites during 2000–2018. The greatest decline was observed in southeastern Canada owing to regional SO2 and NOx reductions. Wet deposition was more important than dry deposition, comprising 71–95 % of total N and 45–89 % of total S deposition. While critical loads (CLs) were exceeded at a few sites in the early 2000s, acidic deposition declined below CLs after 2012, which signifies recovery from legacy acidification.
Hui Zhang, Xuewu Fu, Ben Yu, Baoxin Li, Peng Liu, Guoqing Zhang, Leiming Zhang, and Xinbin Feng
Atmos. Chem. Phys., 21, 15847–15859, https://doi.org/10.5194/acp-21-15847-2021, https://doi.org/10.5194/acp-21-15847-2021, 2021
Short summary
Short summary
Our observations of speciated atmospheric mercury at the Waliguan GAW Baseline Observatory show that concentrations of gaseous elemental mercury (GEM) and particulate bound mercury (PBM) were elevated compared to the Northern Hemisphere background. We propose that the major sources of GEM and PBM were mainly related to anthropogenic emissions and desert dust sources. This study highlights that dust-related sources played an important role in the variations of PBM in the Tibetan Plateau.
Zhiyong Wu, Leiming Zhang, John T. Walker, Paul A. Makar, Judith A. Perlinger, and Xuemei Wang
Geosci. Model Dev., 14, 5093–5105, https://doi.org/10.5194/gmd-14-5093-2021, https://doi.org/10.5194/gmd-14-5093-2021, 2021
Short summary
Short summary
A community dry deposition algorithm for modeling the gaseous dry deposition process in chemistry transport models was extended to include an additional 12 oxidized volatile organic compounds and hydrogen cyanide based on their physicochemical properties and was then evaluated using field flux measurements over a mixed forest. This study provides a useful tool that is needed in chemistry transport models with increasing complexity for simulating an important atmospheric process.
Katherine Hayden, Shao-Meng Li, Paul Makar, John Liggio, Samar G. Moussa, Ayodeji Akingunola, Robert McLaren, Ralf M. Staebler, Andrea Darlington, Jason O'Brien, Junhua Zhang, Mengistu Wolde, and Leiming Zhang
Atmos. Chem. Phys., 21, 8377–8392, https://doi.org/10.5194/acp-21-8377-2021, https://doi.org/10.5194/acp-21-8377-2021, 2021
Short summary
Short summary
We developed a method using aircraft measurements to determine lifetimes with respect to dry deposition for oxidized sulfur and nitrogen compounds over the boreal forest in Alberta, Canada. Atmospheric lifetimes were significantly shorter than derived from chemical transport models with differences related to modelled dry deposition velocities. The shorter lifetimes suggest models need to reassess dry deposition treatment and predictions of sulfur and nitrogen in the atmosphere and ecosystems.
Xuewu Fu, Chen Liu, Hui Zhang, Yue Xu, Hui Zhang, Jun Li, Xiaopu Lyu, Gan Zhang, Hai Guo, Xun Wang, Leiming Zhang, and Xinbin Feng
Atmos. Chem. Phys., 21, 6721–6734, https://doi.org/10.5194/acp-21-6721-2021, https://doi.org/10.5194/acp-21-6721-2021, 2021
Short summary
Short summary
TGM concentrations and isotopic compositions in 10 Chinese cities showed strong seasonality with higher TGM concentrations and Δ199Hg and lower δ202Hg in summer. We found the seasonal variations in TGM concentrations and isotopic compositions were highly related to regional surface Hg(0) emissions, suggesting land surface Hg(0) emissions are an important source of atmospheric TGM that contribute dominantly to the seasonal variations in TGM concentrations and isotopic compositions.
Xiaofei Qin, Leiming Zhang, Guochen Wang, Xiaohao Wang, Qingyan Fu, Jian Xu, Hao Li, Jia Chen, Qianbiao Zhao, Yanfen Lin, Juntao Huo, Fengwen Wang, Kan Huang, and Congrui Deng
Atmos. Chem. Phys., 20, 10985–10996, https://doi.org/10.5194/acp-20-10985-2020, https://doi.org/10.5194/acp-20-10985-2020, 2020
Short summary
Short summary
The uncertainties in mercury emissions are much larger from natural sources than anthropogenic sources. A method was developed to quantify the contributions of natural surface emissions to ambient GEM based on PMF modeling. The annual GEM concentration in eastern China showed a decreasing trend from 2015 to 2018, while the relative contribution of natural surface emissions increased significantly from 41 % in 2015 to 57 % in 2018, gradually surpassing those from anthropogenic sources.
Xiaohong Yao and Leiming Zhang
Atmos. Chem. Phys., 20, 721–733, https://doi.org/10.5194/acp-20-721-2020, https://doi.org/10.5194/acp-20-721-2020, 2020
Short summary
Short summary
An innovative approach is developed to preprocess monitored wet deposition data of inorganic ions for generating their decadal trends. Differing from traditional approaches which directly apply annual or seasonal average data to trend analysis tools, the proposed new approach makes use of slopes of regression equations between a series of study years and a climatology (base) year in terms of monthly averaged data. The new approach yields more robust results than the traditional tools.
Jun Tao, Zhisheng Zhang, Yunfei Wu, Leiming Zhang, Zhijun Wu, Peng Cheng, Mei Li, Laiguo Chen, Renjian Zhang, and Junji Cao
Atmos. Chem. Phys., 19, 8471–8490, https://doi.org/10.5194/acp-19-8471-2019, https://doi.org/10.5194/acp-19-8471-2019, 2019
Short summary
Short summary
Mass-scattering efficiencies (MSE) of dominant chemical species in atmospheric aerosols are important parameters for building the relationships between chemical species and the particle-scattering coefficient. Particle MSE mainly depends on the mass fractions of (NH4)2SO4, NH4NO3, and organic matter and their MSEs in the droplet mode. MSEs of (NH4)2SO4, NH4NO3 and organic matter were determined by their size distributions in the droplet mode.
Xiaohong Xu, Tianchu Zhang, and Yushan Su
Atmos. Chem. Phys., 19, 7335–7345, https://doi.org/10.5194/acp-19-7335-2019, https://doi.org/10.5194/acp-19-7335-2019, 2019
Short summary
Short summary
This study investigates temporal variations and long-term trends in O3 (ozone) and its precursors in Windsor, Canada. During the 1996–2015 period, NOx (nitric oxides) and non-methane hydrocarbon concentrations decreased by 58 % and 61 %, respectively. Annual O3 concentrations increased by 33 % due to (1) decreased O3 titration owing to declining NOx concentrations, (2) reduced local photochemical production of O3 because of dwindling precursor emissions, and (3) increased background O3 level.
Yang Chen, Mi Tian, Ru-Jin Huang, Guangming Shi, Huanbo Wang, Chao Peng, Junji Cao, Qiyuan Wang, Shumin Zhang, Dongmei Guo, Leiming Zhang, and Fumo Yang
Atmos. Chem. Phys., 19, 3245–3255, https://doi.org/10.5194/acp-19-3245-2019, https://doi.org/10.5194/acp-19-3245-2019, 2019
Short summary
Short summary
Amine-containing particles were characterized in an urban area of Chongqing during both summer and winter using a single-particle aerosol mass spectrometer (SPAMS). Amines were observed to internally mix with elemental carbon (EC), organic carbon (OC), sulfate, and nitrate. Diethylamine (DEA) was the most abundant in both number and peak area among amine-containing particles. Vegetation and traffic were the primary sources of particulate amines.
Xin Qiu, Irene Cheng, Fuquan Yang, Erin Horb, Leiming Zhang, and Tom Harner
Atmos. Chem. Phys., 18, 3457–3467, https://doi.org/10.5194/acp-18-3457-2018, https://doi.org/10.5194/acp-18-3457-2018, 2018
Short summary
Short summary
We developed emissions databases for polycyclic aromatic compounds (PACs) in the Athabasca oil sands region and evaluated the emissions databases by comparing CALPUFF-modelled concentrations with monitored data. Model–measurement agreement improved near oil sands mines due to updated PAC emissions from tailings ponds. Modelled concentrations were underestimated at remote sites and for alkylated PACs suggesting that the emissions of PACs particularly alkylated compounds are underestimated.
Cynthia H. Whaley, Paul A. Makar, Mark W. Shephard, Leiming Zhang, Junhua Zhang, Qiong Zheng, Ayodeji Akingunola, Gregory R. Wentworth, Jennifer G. Murphy, Shailesh K. Kharol, and Karen E. Cady-Pereira
Atmos. Chem. Phys., 18, 2011–2034, https://doi.org/10.5194/acp-18-2011-2018, https://doi.org/10.5194/acp-18-2011-2018, 2018
Short summary
Short summary
Using a modified air quality forecasting model, we have found that a significant fraction (> 50 %) of ambient ammonia comes from re-emission from plants and soils in the broader Athabasca Oil Sands region and much of Alberta and Saskatchewan. We also found that about 20 % of ambient ammonia in Alberta and Saskatchewan came from forest fires in the summer of 2013. The addition of these two processes improved modelled ammonia, which was a motivating factor in undertaking this research.
Huanbo Wang, Mi Tian, Yang Chen, Guangming Shi, Yuan Liu, Fumo Yang, Leiming Zhang, Liqun Deng, Jiayan Yu, Chao Peng, and Xuyao Cao
Atmos. Chem. Phys., 18, 865–881, https://doi.org/10.5194/acp-18-865-2018, https://doi.org/10.5194/acp-18-865-2018, 2018
Huiting Mao, Dolly Hall, Zhuyun Ye, Ying Zhou, Dirk Felton, and Leiming Zhang
Atmos. Chem. Phys., 17, 11655–11671, https://doi.org/10.5194/acp-17-11655-2017, https://doi.org/10.5194/acp-17-11655-2017, 2017
Short summary
Short summary
Mercury (Hg) is a global pollutant hazardous to human and ecosystem health, and its emission control is imperative. Anthropogenic mercury emissions have been reduced by 78 % in the United States from 1990 to 2014. However, no clearly defined trend was observed in Hg concentrations at urban locations such as the one in this study. This indicates that other factors may have dominated over anthropogenic emission control. The implications of this study could hence be highly policy relevant.
Jun Tao, Leiming Zhang, Junji Cao, and Renjian Zhang
Atmos. Chem. Phys., 17, 9485–9518, https://doi.org/10.5194/acp-17-9485-2017, https://doi.org/10.5194/acp-17-9485-2017, 2017
Short summary
Short summary
In this study, studies on PM2.5 chemical composition, source apportionment and its impact on aerosol optical properties across China are thoroughly reviewed, and historical emission control policies in China and their effectiveness in reducing PM2.5 are discussed.
Leiming Zhang, Seth Lyman, Huiting Mao, Che-Jen Lin, David A. Gay, Shuxiao Wang, Mae Sexauer Gustin, Xinbin Feng, and Frank Wania
Atmos. Chem. Phys., 17, 9133–9144, https://doi.org/10.5194/acp-17-9133-2017, https://doi.org/10.5194/acp-17-9133-2017, 2017
Short summary
Short summary
Future research needs are proposed for improving the understanding of atmospheric mercury cycling. These include refinement of mercury emission estimations, quantification of dry deposition and air–surface exchange, improvement of the treatment of chemical mechanisms in chemical transport models, increase in the accuracy of oxidized mercury measurements, better interpretation of atmospheric mercury chemistry data, and harmonization of network operation.
Yunfei Wu, Xiaojia Wang, Jun Tao, Rujin Huang, Ping Tian, Junji Cao, Leiming Zhang, Kin-Fai Ho, Zhiwei Han, and Renjian Zhang
Atmos. Chem. Phys., 17, 7965–7975, https://doi.org/10.5194/acp-17-7965-2017, https://doi.org/10.5194/acp-17-7965-2017, 2017
Short summary
Short summary
As black carbon (BC) aerosols play an important role in the climate and environment, the size distribution of refractory BC (rBC) was investigated. On this basis, the source of rBC was further analyzed. The local traffic exhausts contributed greatly to the rBC in urban areas. However, its contribution decreased significantly in the polluted period compared to the clean period, implying the increasing contribution of other sources, e.g., coal combustion or biomass burning, in the polluted period.
Irene Cheng and Leiming Zhang
Atmos. Chem. Phys., 17, 4711–4730, https://doi.org/10.5194/acp-17-4711-2017, https://doi.org/10.5194/acp-17-4711-2017, 2017
Short summary
Short summary
Geographical and long-term (1983–2011) trends in air concentrations and wet deposition of inorganic ions and aerosol and precipitation acidity were analyzed at 31 sites in Canada. Declines in atmospheric ammonium, nitrate, and sulfate were consistent with decreasing emissions of NH3, NOx, and SO2. A decline in nitrate and sulfate wet deposition was also observed. Wet scavenging was further studied by estimating scavenging ratios and relative contributions of gases and aerosols to wet deposition.
Xiaohong Xu, Yanyin Liao, Irene Cheng, and Leiming Zhang
Atmos. Chem. Phys., 17, 1381–1400, https://doi.org/10.5194/acp-17-1381-2017, https://doi.org/10.5194/acp-17-1381-2017, 2017
Short summary
Short summary
This study addresses two issues related to source–receptor analysis of speciated atmospheric mercury: (1) comparing PMF and PCA and (2) testing different approaches in data selection for PMF modeling.
L. Paige Wright, Leiming Zhang, and Frank J. Marsik
Atmos. Chem. Phys., 16, 13399–13416, https://doi.org/10.5194/acp-16-13399-2016, https://doi.org/10.5194/acp-16-13399-2016, 2016
Short summary
Short summary
The current knowledge concerning mercury dry deposition is reviewed, including dry deposition algorithms used in chemical transport models and at monitoring sites, measurement methods and studies for quantifying dry deposition of oxidized mercury, and measurement studies of litterfall and throughfall mercury. Over all the regions, dry deposition, estimated as the sum of litterfall and throughfall minus open-field wet deposition, is more dominant than wet deposition for Hg deposition.
Huiting Mao, Irene Cheng, and Leiming Zhang
Atmos. Chem. Phys., 16, 12897–12924, https://doi.org/10.5194/acp-16-12897-2016, https://doi.org/10.5194/acp-16-12897-2016, 2016
Short summary
Short summary
Understanding of spatial and temporal variations of atmospheric speciated mercury can advance our knowledge of mercury cycling in various environments. This review summarized spatiotemporal variations of TGM/GEM, GOM, and PBM in environments including oceans, continents, high elevation, the free troposphere, and low to high latitudes. Remaining questions/issues and recommendations were provided for future research.
Xiaohong Yao and Leiming Zhang
Atmos. Chem. Phys., 16, 11465–11475, https://doi.org/10.5194/acp-16-11465-2016, https://doi.org/10.5194/acp-16-11465-2016, 2016
Short summary
Short summary
Atmospheric NH3 plays an important role in forming secondary aerosols and has a direct impact on sensitive ecosystems. This study aims to study its long-term variation and find that the long-term trend can be affected by climate change as well as other anthropogenic factors, depending on sites. A large percentage increase of atmospheric NH3 at remote American sites is surprising and may cause a potential threat to sensitive ecosystems in the future.
Xiaodong Zhang, Tao Huang, Leiming Zhang, Yanjie Shen, Yuan Zhao, Hong Gao, Xiaoxuan Mao, Chenhui Jia, and Jianmin Ma
Atmos. Chem. Phys., 16, 6949–6960, https://doi.org/10.5194/acp-16-6949-2016, https://doi.org/10.5194/acp-16-6949-2016, 2016
Short summary
Short summary
This paper assesses long-term trend of biogenic isoprene emissions in the Three-North Shelter Forest Program, also known as "the Green Great Wall", the largest artificial afforestation in the human history. Results show that the TNRSF has altered the long-term emission trend in north China from a decreasing to an increasing trend from 1982 to 2010. Isoprene emission fluxes have increased in many places of the TNRSF over the last 3 decades due to the growing trees and vegetation coverage.
Lei Zhang, Shuxiao Wang, Qingru Wu, Fengyang Wang, Che-Jen Lin, Leiming Zhang, Mulin Hui, Mei Yang, Haitao Su, and Jiming Hao
Atmos. Chem. Phys., 16, 2417–2433, https://doi.org/10.5194/acp-16-2417-2016, https://doi.org/10.5194/acp-16-2417-2016, 2016
C. G. Nolte, K. W. Appel, J. T. Kelly, P. V. Bhave, K. M. Fahey, J. L. Collett Jr., L. Zhang, and J. O. Young
Geosci. Model Dev., 8, 2877–2892, https://doi.org/10.5194/gmd-8-2877-2015, https://doi.org/10.5194/gmd-8-2877-2015, 2015
Short summary
Short summary
This study is the most comprehensive evaluation of CMAQ inorganic
aerosol size-composition distributions conducted to date. We compare two
methods of inferring PM2.5 concentrations from the model: (1) based on
the sum of the masses in the fine aerosol modes, as is most commonly
done in CMAQ model evaluation; and (2) computed using the simulated size
distributions. Differences are generally less than 1 microgram/m3, and
are largest over the eastern USA during the summer.
Z. Y. Wu, L. Zhang, X. M. Wang, and J. W. Munger
Atmos. Chem. Phys., 15, 7487–7496, https://doi.org/10.5194/acp-15-7487-2015, https://doi.org/10.5194/acp-15-7487-2015, 2015
Short summary
Short summary
In this study, we have developed a modified micrometeorological gradient method (MGM), although based on existing micrometeorological theory, to estimate O3 dry deposition fluxes over a forest canopy using concentration gradients between a level above and a level below the canopy top. The new method provides an alternative approach in monitoring/estimating long-term deposition fluxes of similar pollutants over tall canopies and is expected to be useful for the scientific community.
L. Zhang, I. Cheng, D. Muir, and J.-P. Charland
Atmos. Chem. Phys., 15, 1421–1434, https://doi.org/10.5194/acp-15-1421-2015, https://doi.org/10.5194/acp-15-1421-2015, 2015
Short summary
Short summary
This study analyzed air and precipitation concentrations of 43 polycyclic aromatic compounds (PACs) collected in the Athabasca oil sands region. A database has been built for the parameter scavenging ratio, which is defined as the ratio of the concentration of PACs in precipitation to that in air. A better understanding of the potential differences between gas and particulate scavenging and between snow and rain scavenging has been achieved.
J. Tao, J. Gao, L. Zhang, R. Zhang, H. Che, Z. Zhang, Z. Lin, J. Jing, J. Cao, and S.-C. Hsu
Atmos. Chem. Phys., 14, 8679–8699, https://doi.org/10.5194/acp-14-8679-2014, https://doi.org/10.5194/acp-14-8679-2014, 2014
Z. J. Lin, Z. S. Zhang, L. Zhang, J. Tao, R. J. Zhang, J. J. Cao, S. J. Fan, and Y. H. Zhang
Atmos. Chem. Phys., 14, 7631–7644, https://doi.org/10.5194/acp-14-7631-2014, https://doi.org/10.5194/acp-14-7631-2014, 2014
D. Wen, L. Zhang, J. C. Lin, R. Vet, and M. D. Moran
Geosci. Model Dev., 7, 1037–1050, https://doi.org/10.5194/gmd-7-1037-2014, https://doi.org/10.5194/gmd-7-1037-2014, 2014
X. Wang, L. Zhang, and M. D. Moran
Geosci. Model Dev., 7, 799–819, https://doi.org/10.5194/gmd-7-799-2014, https://doi.org/10.5194/gmd-7-799-2014, 2014
L. Zhang and Z. He
Atmos. Chem. Phys., 14, 3729–3737, https://doi.org/10.5194/acp-14-3729-2014, https://doi.org/10.5194/acp-14-3729-2014, 2014
X. H. Yao and L. Zhang
Biogeosciences, 10, 7913–7925, https://doi.org/10.5194/bg-10-7913-2013, https://doi.org/10.5194/bg-10-7913-2013, 2013
S. Chen, X. Qiu, L. Zhang, F. Yang, and P. Blanchard
Atmos. Chem. Phys., 13, 11287–11293, https://doi.org/10.5194/acp-13-11287-2013, https://doi.org/10.5194/acp-13-11287-2013, 2013
L. Zhang, X. Wang, M. D. Moran, and J. Feng
Atmos. Chem. Phys., 13, 10005–10025, https://doi.org/10.5194/acp-13-10005-2013, https://doi.org/10.5194/acp-13-10005-2013, 2013
I. Cheng, L. Zhang, P. Blanchard, J. Dalziel, and R. Tordon
Atmos. Chem. Phys., 13, 6031–6048, https://doi.org/10.5194/acp-13-6031-2013, https://doi.org/10.5194/acp-13-6031-2013, 2013
G. Kos, A. Ryzhkov, A. Dastoor, J. Narayan, A. Steffen, P. A. Ariya, and L. Zhang
Atmos. Chem. Phys., 13, 4839–4863, https://doi.org/10.5194/acp-13-4839-2013, https://doi.org/10.5194/acp-13-4839-2013, 2013
D. Wen, J. C. Lin, L. Zhang, R. Vet, and M. D. Moran
Geosci. Model Dev., 6, 327–344, https://doi.org/10.5194/gmd-6-327-2013, https://doi.org/10.5194/gmd-6-327-2013, 2013
Related subject area
Subject: Gases | Research Activity: Atmospheric Modelling and Data Analysis | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Investigating the response of China's surface ozone concentration to the future changes of multiple factors
Assessing the relative impacts of satellite ozone and its precursor observations to improve global tropospheric ozone analysis using multiple chemical reanalysis systems
Evaluating present-day and future impacts of agricultural ammonia emissions on atmospheric chemistry and climate
Air-pollution-satellite-based CO2 emission inversion: system evaluation, sensitivity analysis, and future research direction
Insights into ozone pollution control in urban areas by decoupling meteorological factors based on machine learning
Quantification of regional net CO2 flux errors in the Orbiting Carbon Observatory-2 (OCO-2) v10 model intercomparison project (MIP) ensemble using airborne measurements
Reactive nitrogen in and around the northeastern and mid-Atlantic US: sources, sinks, and connections with ozone
Preindustrial-to-present-day changes in atmospheric carbon monoxide: agreement and gaps between ice archives and global model reconstructions
Investigating processes influencing simulation of local Arctic wintertime anthropogenic pollution in Fairbanks, Alaska, during ALPACA-2022
Urban ozone formation and sensitivities to volatile chemical products, cooking emissions, and NOx upwind of and within two Los Angeles Basin cities
Causes of growing middle-to-upper tropospheric ozone over the northwest Pacific region
Impact of introducing electric vehicles on ground-level O3 and PM2.5 in the Greater Tokyo Area: yearly trends and the importance of changes in the urban heat island effect
A CO2–Δ14CO2 inversion setup for estimating European fossil CO2 emissions
Maximum ozone concentrations in the southwestern US and Texas: implications of the growing predominance of the background contribution
Derivation of atmospheric reaction mechanisms for volatile organic compounds by the SAPRC mechanism generation system (MechGen)
Seasonal, regional, and vertical characteristics of high-carbon-monoxide plumes along with their associated ozone anomalies, as seen by IAGOS between 2002 and 2019
The potential of drone observations to improve air quality predictions by 4D-Var
Process analysis of elevated concentrations of organic acids at Whiteface Mountain, New York
Ozone source attribution in polluted European areas during summer 2017 as simulated with MECO(n)
Opinion: Challenges and needs of tropospheric chemical mechanism development
The atmospheric oxidizing capacity in China – Part 2: Sensitivity to emissions of primary pollutants
Role of chemical production and depositional losses on formaldehyde in the Community Regional Atmospheric Chemistry Multiphase Mechanism (CRACMM)
Review of source analyses of ambient volatile organic compounds considering reactive losses: methods of reducing loss effects, impacts of losses, and sources
Interpreting summertime hourly variation of NO2 columns with implications for geostationary satellite applications
An investigation into atmospheric nitrous acid (HONO) processes in South Korea
Performance evaluation of UKESM1 for surface ozone across the pan-tropics
Constraining light dependency in modeled emissions through comparison to observed biogenic volatile organic compound (BVOC) concentrations in a southeastern US forest
A global re-analysis of regionally resolved emissions and atmospheric mole fractions of SF6 for the period 2005–2021
Monoterpene oxidation pathways initiated by acyl peroxy radical addition
Tropospheric ozone precursors: global and regional distributions, trends, and variability
Sensitivity of climate effects of hydrogen to leakage size, location, and chemical background
The contribution of transport emissions to ozone mixing ratios and methane lifetime in 2015 and 2050 in the Shared Socioeconomic Pathways (SSPs)
Local and transboundary contributions to nitrogen loadings across East Asia using CMAQ-ISAM and GEMS-informed emissions inventory during the winter-spring transition
Ether and ester formation from peroxy radical recombination: a qualitative reaction channel analysis
ACEIC: a comprehensive anthropogenic chlorine emission inventory for China
Impact of methane and other precursor emission reductions on surface ozone in Europe: scenario analysis using the European Monitoring and Evaluation Programme (EMEP) Meteorological Synthesizing Centre – West (MSC-W) model
Chemistry-climate feedback of atmospheric methane in a methane emission flux driven chemistry-climate model
Natural emissions of VOC and NOx over Africa constrained by TROPOMI HCHO and NO2 data using the MAGRITTEv1.1 model
Verifying national inventory-based combustion emissions of CO2 across the UK and mainland Europe using satellite observations of atmospheric CO and CO2
Revisiting the high tropospheric ozone over Southern Africa: overestimated biomass burning and underestimated anthropogenic emissions
Enhanced understanding of atmospheric blocking modulation on ozone dynamics within a high-resolution Earth system model
Estimating the variability of NOx emissions from Wuhan with TROPOMI NO2 data during 2018 to 2023
An improved estimate of inorganic iodine emissions from the ocean using a coupled surface microlayer box model
Technical note: A comparative study of chemistry schemes for volcanic sulfur dioxide in Lagrangian transport simulations: a case study of the 2019 Raikoke eruption
Evaluating tropospheric nitrogen dioxide in UKCA using OMI satellite retrievals over South and East Asia
Impact of improved representation of volatile organic compound emissions and production of NOx reservoirs on modeled urban ozone production
The effect of different climate and air quality policies in China on in situ ozone production in Beijing
Enhancing long-term trend simulation of the global tropospheric hydroxyl (TOH) and its drivers from 2005 to 2019: a synergistic integration of model simulations and satellite observations
Intercomparison of GEOS-Chem and CAM-chem tropospheric oxidant chemistry within the Community Earth System Model version 2 (CESM2)
Development of a detailed gaseous oxidation scheme of naphthalene for secondary organic aerosol (SOA) formation and speciation
Jinya Yang, Yutong Wang, Lei Zhang, and Yu Zhao
Atmos. Chem. Phys., 25, 2649–2666, https://doi.org/10.5194/acp-25-2649-2025, https://doi.org/10.5194/acp-25-2649-2025, 2025
Short summary
Short summary
We develop a modeling framework to predict future ozone concentrations (till the 2060s) in China following an IPCC scenario. We evaluate the contributions of climatic, anthropogenic, and biogenic factors by season and region. We find persistent emission controls will alter the nonlinear response of ozone to its precursors and dominate the declining ozone level. The outcomes highlight the importance of human actions, even with a climate penalty on air quality.
Takashi Sekiya, Emanuele Emili, Kazuyuki Miyazaki, Antje Inness, Zhen Qu, R. Bradley Pierce, Dylan Jones, Helen Worden, William Y. Y. Cheng, Vincent Huijnen, and Gerbrand Koren
Atmos. Chem. Phys., 25, 2243–2268, https://doi.org/10.5194/acp-25-2243-2025, https://doi.org/10.5194/acp-25-2243-2025, 2025
Short summary
Short summary
Five global chemical reanalysis datasets were used to assess the relative impacts of assimilating satellite ozone and its precursor measurements on tropospheric ozone analyses for 2010. The multiple reanalysis system comparison allows an evaluation of the dependency of the impacts on different reanalysis systems. The results suggested the importance of satellite ozone and its precursor measurements for improving ozone analysis in the whole troposphere, with varying magnitudes among the systems.
Maureen Beaudor, Didier Hauglustaine, Juliette Lathière, Martin Van Damme, Lieven Clarisse, and Nicolas Vuichard
Atmos. Chem. Phys., 25, 2017–2046, https://doi.org/10.5194/acp-25-2017-2025, https://doi.org/10.5194/acp-25-2017-2025, 2025
Short summary
Short summary
Agriculture is the biggest ammonia (NH3) source, impacting air quality, climate, and ecosystems. Because of food demand, NH3 emissions are projected to rise by 2100. Using a global model, we analyzed the impact of present and future NH3 emissions generated from a land model. Our results show improved ammonia patterns compared to a reference inventory. Future scenarios predict up to 70 % increase in global NH3 burden, with significant changes in radiative forcing that can greatly elevate N2O.
Hui Li, Jiaxin Qiu, and Bo Zheng
Atmos. Chem. Phys., 25, 1949–1963, https://doi.org/10.5194/acp-25-1949-2025, https://doi.org/10.5194/acp-25-1949-2025, 2025
Short summary
Short summary
We conduct a sensitivity analysis with 31 tests on various factors including prior emissions, model resolution, satellite constraint, and other system configurations to assess the vulnerability of emission estimates across temporal, sectoral, and regional dimensions. This reveals the robustness of emissions estimated by this air-pollution-satellite-based CO2 emission inversion system, with relative change between tests and base inversion below 4.0 % for national annual NOx and CO2 emissions.
Yuqing Qiu, Xin Li, Wenxuan Chai, Yi Liu, Mengdi Song, Xudong Tian, Qiaoli Zou, Wenjun Lou, Wangyao Zhang, Juan Li, and Yuanhang Zhang
Atmos. Chem. Phys., 25, 1749–1763, https://doi.org/10.5194/acp-25-1749-2025, https://doi.org/10.5194/acp-25-1749-2025, 2025
Short summary
Short summary
The chemical reactions of ozone (O3) formation are related to meteorology and local emissions. Here, a random forest approach was used to eliminate the effects of meteorological factors (dispersion or transport) on O3 and its precursors. Variations in the sensitivity of O3 formation and the apportionment of emission sources were revealed after meteorological normalization. Our results suggest that meteorological variations should be considered when diagnosing O3 formation.
Jeongmin Yun, Junjie Liu, Brendan Byrne, Brad Weir, Lesley E. Ott, Kathryn McKain, Bianca C. Baier, Luciana V. Gatti, and Sebastien C. Biraud
Atmos. Chem. Phys., 25, 1725–1748, https://doi.org/10.5194/acp-25-1725-2025, https://doi.org/10.5194/acp-25-1725-2025, 2025
Short summary
Short summary
This study quantifies errors in regional net surface–atmosphere CO2 flux estimates from an inverse model ensemble using airborne CO2 measurements. Our results show that flux error estimates based on observations significantly exceed those computed from the ensemble spread of flux estimates in regions with high fossil fuel emissions. This finding suggests the presence of systematic biases in the inversion estimates, associated with errors in the fossil fuel emissions common to all models.
Min Huang, Gregory R. Carmichael, Kevin W. Bowman, Isabelle De Smedt, Andreas Colliander, Michael H. Cosh, Sujay V. Kumar, Alex B. Guenther, Scott J. Janz, Ryan M. Stauffer, Anne M. Thompson, Niko M. Fedkin, Robert J. Swap, John D. Bolten, and Alicia T. Joseph
Atmos. Chem. Phys., 25, 1449–1476, https://doi.org/10.5194/acp-25-1449-2025, https://doi.org/10.5194/acp-25-1449-2025, 2025
Short summary
Short summary
We use model simulations along with multiplatform, multidisciplinary observations and a range of analysis methods to estimate and understand the distributions, temporal changes, and impacts of reactive nitrogen and ozone over the most populous US region that has undergone significant environmental changes. Deposition, biogenic emissions, and extra-regional sources have been playing increasingly important roles in controlling pollutant budgets in this area as local anthropogenic emissions drop.
Xavier Faïn, Sophie Szopa, Vaishali Naïk, Patricia Martinerie, David M. Etheridge, Rachael H. Rhodes, Cathy M. Trudinger, Vasilii V. Petrenko, Kévin Fourteau, and Philip Place
Atmos. Chem. Phys., 25, 1105–1119, https://doi.org/10.5194/acp-25-1105-2025, https://doi.org/10.5194/acp-25-1105-2025, 2025
Short summary
Short summary
Carbon monoxide (CO) plays a crucial role in the atmosphere's oxidizing capacity. In this study, we analyse how historical (1850–2014) [CO] outputs from state-of-the-art global chemistry–climate models over Greenland and Antarctica are able to capture both absolute values and trends recorded in multi-site ice archives. A disparity in [CO] growth rates emerges in the Northern Hemisphere between models and observations from 1920–1975 CE, possibly linked to uncertainties in CO emission factors.
Natalie Brett, Kathy S. Law, Steve R. Arnold, Javier G. Fochesatto, Jean-Christophe Raut, Tatsuo Onishi, Robert Gilliam, Kathleen Fahey, Deanna Huff, George Pouliot, Brice Barret, Elsa Dieudonné, Roman Pohorsky, Julia Schmale, Andrea Baccarini, Slimane Bekki, Gianluca Pappaccogli, Federico Scoto, Stefano Decesari, Antonio Donateo, Meeta Cesler-Maloney, William Simpson, Patrice Medina, Barbara D'Anna, Brice Temime-Roussel, Joel Savarino, Sarah Albertin, Jingqiu Mao, Becky Alexander, Allison Moon, Peter F. DeCarlo, Vanessa Selimovic, Robert Yokelson, and Ellis S. Robinson
Atmos. Chem. Phys., 25, 1063–1104, https://doi.org/10.5194/acp-25-1063-2025, https://doi.org/10.5194/acp-25-1063-2025, 2025
Short summary
Short summary
Processes influencing dispersion of local anthropogenic pollution in Arctic wintertime are investigated with Lagrangian dispersion modelling. Simulated power plant plume rise that considers temperature inversion layers improves results compared to observations (interior Alaska). Modelled surface concentrations are improved by representation of vertical mixing and emission estimates. Large increases in diesel vehicle emissions at temperatures reaching −35°C are required to reproduce observed NOx.
Chelsea E. Stockwell, Matthew M. Coggon, Rebecca H. Schwantes, Colin Harkins, Bert Verreyken, Congmeng Lyu, Qindan Zhu, Lu Xu, Jessica B. Gilman, Aaron Lamplugh, Jeff Peischl, Michael A. Robinson, Patrick R. Veres, Meng Li, Andrew W. Rollins, Kristen Zuraski, Sunil Baidar, Shang Liu, Toshihiro Kuwayama, Steven S. Brown, Brian C. McDonald, and Carsten Warneke
Atmos. Chem. Phys., 25, 1121–1143, https://doi.org/10.5194/acp-25-1121-2025, https://doi.org/10.5194/acp-25-1121-2025, 2025
Short summary
Short summary
In urban areas, emissions from everyday products like paints, cleaners, and personal care products, along with non-traditional sources such as cooking, are increasingly important and impact air quality. This study uses a box model to evaluate how these emissions impact ozone in the Los Angeles Basin and quantifies the impact of gaseous cooking emissions. Accurate representation of these and other anthropogenic sources in inventories is crucial for informing effective air quality policies.
Xiaodan Ma, Jianping Huang, Michaela I. Hegglin, Patrick Jöckel, and Tianliang Zhao
Atmos. Chem. Phys., 25, 943–958, https://doi.org/10.5194/acp-25-943-2025, https://doi.org/10.5194/acp-25-943-2025, 2025
Short summary
Short summary
Our research explored changes in ozone levels in the northwest Pacific region over 30 years, revealing a significant increase in the middle-to-upper troposphere, especially during spring and summer. This rise is influenced by both stratospheric and tropospheric sources, which affect climate and air quality in East Asia. This work underscores the need for continued study to understand underlying mechanisms.
Hiroo Hata, Norifumi Mizushima, and Tomohiko Ihara
Atmos. Chem. Phys., 25, 1037–1061, https://doi.org/10.5194/acp-25-1037-2025, https://doi.org/10.5194/acp-25-1037-2025, 2025
Short summary
Short summary
The introduction of battery electric vehicles (BEVs) is expected to reduce the primary air pollutants from vehicular exhaust and evaporative emissions while reducing the anthropogenic heat produced by vehicles, ultimately mitigating the urban heat island (UHI) effect. This study revealed the impact of introducing BEVs on the decrease in the UHI effect and the impact of BEVs on the formation of tropospheric ozone and fine particulate matter in the Greater Tokyo Area of Japan.
Carlos Gómez-Ortiz, Guillaume Monteil, Sourish Basu, and Marko Scholze
Atmos. Chem. Phys., 25, 397–424, https://doi.org/10.5194/acp-25-397-2025, https://doi.org/10.5194/acp-25-397-2025, 2025
Short summary
Short summary
In this paper, we test new implementations of our inverse modeling tool to estimate the weekly and regional CO2 emissions from fossil fuels in Europe. We use synthetic atmospheric observations of CO2 and radiocarbon (14CO2) to trace emissions to their sources, while separating the natural and fossil CO2. Our tool accurately estimates fossil CO2 emissions in densely monitored regions like western/central Europe. This approach aids in developing strategies for reducing CO2 emissions.
David D. Parrish, Ian C. Faloona, and Richard G. Derwent
Atmos. Chem. Phys., 25, 263–289, https://doi.org/10.5194/acp-25-263-2025, https://doi.org/10.5194/acp-25-263-2025, 2025
Short summary
Short summary
Observation-based estimates of contributions to maximum ozone (O3) concentrations show that background O3 can exceed the air quality standard of 70 ppb in the southwestern US, precluding standard attainment. Over the past 4 decades, US anthropogenic O3 has decreased by a factor of ~ 6.3, while wildfire contributions have increased, so that the background now dominates maximum concentrations, even in Los Angeles, and the occurrence of maximum O3 has shifted from the eastern to the western US.
William P. L. Carter, Jia Jiang, John J. Orlando, and Kelley C. Barsanti
Atmos. Chem. Phys., 25, 199–242, https://doi.org/10.5194/acp-25-199-2025, https://doi.org/10.5194/acp-25-199-2025, 2025
Short summary
Short summary
This paper describes the scientific basis for gas-phase atmospheric chemical mechanisms derived using the SAPRC mechanism generation system, MechGen. It can derive mechanisms for most organic compounds with C, H, O, or N atoms, including initial reactions of organics with OH, O3, NO3, and O3P or by photolysis, as well as the reactions of the various types of intermediates that are formed. The paper includes a description of areas of uncertainty where additional research and updates are needed.
Thibaut Lebourgeois, Bastien Sauvage, Pawel Wolff, Béatrice Josse, Virginie Marécal, Yasmine Bennouna, Romain Blot, Damien Boulanger, Hannah Clark, Jean-Marc Cousin, Philippe Nedelec, and Valérie Thouret
Atmos. Chem. Phys., 24, 13975–14004, https://doi.org/10.5194/acp-24-13975-2024, https://doi.org/10.5194/acp-24-13975-2024, 2024
Short summary
Short summary
Our study examines intense-carbon-monoxide (CO) pollution events measured by commercial aircraft from the In-service Aircraft for a Global Observing System (IAGOS) research infrastructure. We combine these measurements with the SOFT-IO model to trace the origin of the observed CO. A comprehensive analysis of the geographical origin, source type, seasonal variation, and ozone levels of these pollution events is provided.
Hassnae Erraji, Philipp Franke, Astrid Lampert, Tobias Schuldt, Ralf Tillmann, Andreas Wahner, and Anne Caroline Lange
Atmos. Chem. Phys., 24, 13913–13934, https://doi.org/10.5194/acp-24-13913-2024, https://doi.org/10.5194/acp-24-13913-2024, 2024
Short summary
Short summary
Four-dimensional variational data assimilation allows for the simultaneous optimisation of initial values and emission rates by using trace-gas profiles from drone observations in a regional air quality model. Assimilated profiles positively impact the representation of air pollutants in the model by improving their vertical distribution and ground-level concentrations. This case study highlights the potential of drone data to enhance air quality analyses including local emission evaluation.
Christopher Lawrence, Mary Barth, John Orlando, Paul Casson, Richard Brandt, Daniel Kelting, Elizabeth Yerger, and Sara Lance
Atmos. Chem. Phys., 24, 13693–13713, https://doi.org/10.5194/acp-24-13693-2024, https://doi.org/10.5194/acp-24-13693-2024, 2024
Short summary
Short summary
This work uses chemical transport and box modeling to study the gas- and aqueous-phase production of organic acid concentrations measured in cloud water at the summit of Whiteface Mountain on 1 July 2018. Isoprene was the major source of formic, acetic, and oxalic acid. Gas-phase chemistry greatly underestimated formic and acetic acid, indicating missing sources, while cloud chemistry was a key source of oxalic acid. More studies of organic acids are required to better constrain their sources.
Markus Kilian, Volker Grewe, Patrick Jöckel, Astrid Kerkweg, Mariano Mertens, Andreas Zahn, and Helmut Ziereis
Atmos. Chem. Phys., 24, 13503–13523, https://doi.org/10.5194/acp-24-13503-2024, https://doi.org/10.5194/acp-24-13503-2024, 2024
Short summary
Short summary
Anthropogenic emissions are a major source of precursors of tropospheric ozone. As ozone formation is highly non-linear, we apply a global–regional chemistry–climate model with a source attribution method (tagging) to quantify the contribution of anthropogenic emissions to ozone. Our analysis shows that the contribution of European anthropogenic emissions largely increases during large ozone periods, indicating that emissions from these sectors drive ozone values.
Barbara Ervens, Andrew Rickard, Bernard Aumont, William P. L. Carter, Max McGillen, Abdelwahid Mellouki, John Orlando, Bénédicte Picquet-Varrault, Paul Seakins, William R. Stockwell, Luc Vereecken, and Timothy J. Wallington
Atmos. Chem. Phys., 24, 13317–13339, https://doi.org/10.5194/acp-24-13317-2024, https://doi.org/10.5194/acp-24-13317-2024, 2024
Short summary
Short summary
Chemical mechanisms describe the chemical processes in atmospheric models that are used to describe the changes in the atmospheric composition. Therefore, accurate chemical mechanisms are necessary to predict the evolution of air pollution and climate change. The article describes all steps that are needed to build chemical mechanisms and discusses the advances and needs of experimental and theoretical research activities needed to build reliable chemical mechanisms.
Jianing Dai, Guy P. Brasseur, Mihalis Vrekoussis, Maria Kanakidou, Kun Qu, Yijuan Zhang, Hongliang Zhang, and Tao Wang
Atmos. Chem. Phys., 24, 12943–12962, https://doi.org/10.5194/acp-24-12943-2024, https://doi.org/10.5194/acp-24-12943-2024, 2024
Short summary
Short summary
This paper employs a regional chemical transport model to quantify the sensitivity of air pollutants and photochemical parameters to specified emission reductions in China for representative winter and summer conditions. The study provides insights into further air quality control in China with reduced primary emissions.
T. Nash Skipper, Emma L. D'Ambro, Forwood C. Wiser, V. Faye McNeill, Rebecca H. Schwantes, Barron H. Henderson, Ivan R. Piletic, Colleen B. Baublitz, Jesse O. Bash, Andrew R. Whitehill, Lukas C. Valin, Asher P. Mouat, Jennifer Kaiser, Glenn M. Wolfe, Jason M. St. Clair, Thomas F. Hanisco, Alan Fried, Bryan K. Place, and Havala O.T. Pye
Atmos. Chem. Phys., 24, 12903–12924, https://doi.org/10.5194/acp-24-12903-2024, https://doi.org/10.5194/acp-24-12903-2024, 2024
Short summary
Short summary
We develop the Community Regional Atmospheric Chemistry Multiphase Mechanism (CRACMM) version 2 to improve predictions of formaldehyde in ambient air compared to satellite-, aircraft-, and ground-based observations. With the updated chemistry, we estimate the cancer risk from inhalation exposure to ambient formaldehyde across the contiguous USA and predict that 40 % of this risk is controllable through reductions in anthropogenic emissions of nitrogen oxides and reactive organic carbon.
Baoshuang Liu, Yao Gu, Yutong Wu, Qili Dai, Shaojie Song, Yinchang Feng, and Philip K. Hopke
Atmos. Chem. Phys., 24, 12861–12879, https://doi.org/10.5194/acp-24-12861-2024, https://doi.org/10.5194/acp-24-12861-2024, 2024
Short summary
Short summary
Reactive loss of volatile organic compounds (VOCs) is a long-term issue yet to be resolved in VOC source analyses. We assess common methods of, and existing issues in, reducing losses, impacts of losses, and sources in current source analyses. We offer a potential supporting role for solving issues of VOC conversion. Source analyses of consumed VOCs that reacted to produce ozone and secondary organic aerosols can play an important role in the effective control of secondary pollution in air.
Deepangsu Chatterjee, Randall V. Martin, Chi Li, Dandan Zhang, Haihui Zhu, Daven K. Henze, James H. Crawford, Ronald C. Cohen, Lok N. Lamsal, and Alexander M. Cede
Atmos. Chem. Phys., 24, 12687–12706, https://doi.org/10.5194/acp-24-12687-2024, https://doi.org/10.5194/acp-24-12687-2024, 2024
Short summary
Short summary
We investigate the hourly variation of NO2 columns and surface concentrations by applying the GEOS-Chem model to interpret aircraft and ground-based measurements over the US and Pandora sun photometer measurements over the US, Europe, and Asia. Corrections to the Pandora columns and finer model resolution improve the modeled representation of the summertime hourly variation of total NO2 columns to explain the weaker hourly variation in NO2 columns than at the surface.
Kiyeon Kim, Kyung Man Han, Chul Han Song, Hyojun Lee, Ross Beardsley, Jinhyeok Yu, Greg Yarwood, Bonyoung Koo, Jasper Madalipay, Jung-Hun Woo, and Seogju Cho
Atmos. Chem. Phys., 24, 12575–12593, https://doi.org/10.5194/acp-24-12575-2024, https://doi.org/10.5194/acp-24-12575-2024, 2024
Short summary
Short summary
We incorporated each HONO process into the current CMAQ modeling framework to enhance the accuracy of HONO mixing ratio predictions. These results expand our understanding of HONO photochemistry and identify crucial sources of HONO that impact the total HONO budget in Seoul, South Korea. Through this investigation, we contribute to resolving discrepancies in understanding chemical transport models, with implications for better air quality management and environmental protection in the region.
Flossie Brown, Gerd Folberth, Stephen Sitch, Paulo Artaxo, Marijn Bauters, Pascal Boeckx, Alexander W. Cheesman, Matteo Detto, Ninong Komala, Luciana Rizzo, Nestor Rojas, Ines dos Santos Vieira, Steven Turnock, Hans Verbeeck, and Alfonso Zambrano
Atmos. Chem. Phys., 24, 12537–12555, https://doi.org/10.5194/acp-24-12537-2024, https://doi.org/10.5194/acp-24-12537-2024, 2024
Short summary
Short summary
Ozone is a pollutant that is detrimental to human and plant health. Ozone monitoring sites in the tropics are limited, so models are often used to understand ozone exposure. We use measurements from the tropics to evaluate ozone from the UK Earth system model, UKESM1. UKESM1 is able to capture the pattern of ozone in the tropics, except in southeast Asia, although it systematically overestimates it at all sites. This work highlights that UKESM1 can capture seasonal and hourly variability.
Namrata Shanmukh Panji, Deborah F. McGlynn, Laura E. R. Barry, Todd M. Scanlon, Manuel T. Lerdau, Sally E. Pusede, and Gabriel Isaacman-VanWertz
Atmos. Chem. Phys., 24, 12495–12507, https://doi.org/10.5194/acp-24-12495-2024, https://doi.org/10.5194/acp-24-12495-2024, 2024
Short summary
Short summary
Climate change will bring about changes in parameters that are currently used in global-scale models to calculate biogenic emissions. This study seeks to understand the factors driving these models by comparing long-term datasets of biogenic compounds to modeled emissions. We note that the light-dependent fractions currently used in models do not accurately represent regional observations. We provide evidence for the time-dependent variation in this parameter for future modifications to models.
Martin Vojta, Andreas Plach, Saurabh Annadate, Sunyoung Park, Gawon Lee, Pallav Purohit, Florian Lindl, Xin Lan, Jens Mühle, Rona L. Thompson, and Andreas Stohl
Atmos. Chem. Phys., 24, 12465–12493, https://doi.org/10.5194/acp-24-12465-2024, https://doi.org/10.5194/acp-24-12465-2024, 2024
Short summary
Short summary
We constrain the global emissions of the very potent greenhouse gas sulfur hexafluoride (SF6) between 2005 and 2021. We show that SF6 emissions are decreasing in the USA and in the EU, while they are substantially growing in China, leading overall to an increasing global emission trend. The national reports for the USA, EU, and China all underestimated their SF6 emissions. However, stringent mitigation measures can successfully reduce SF6 emissions, as can be seen in the EU emission trend.
Dominika Pasik, Thomas Golin Almeida, Emelda Ahongshangbam, Siddharth Iyer, and Nanna Myllys
EGUsphere, https://doi.org/10.5194/egusphere-2024-3464, https://doi.org/10.5194/egusphere-2024-3464, 2024
Short summary
Short summary
We used quantum chemistry methods to investigate the oxidation mechanisms of acyl peroxy radicals (APRs) with various monoterpenes. Our findings reveal unique oxidation pathways for different monoterpenes, leading to either chain-terminating products or highly reactive intermediates that can contribute to particle formation in the atmosphere. This research highlights APRs as potentially significant but underexplored atmospheric oxidants, which may influence future approaches to modeling climate.
Yasin Elshorbany, Jerald R. Ziemke, Sarah Strode, Hervé Petetin, Kazuyuki Miyazaki, Isabelle De Smedt, Kenneth Pickering, Rodrigo J. Seguel, Helen Worden, Tamara Emmerichs, Domenico Taraborrelli, Maria Cazorla, Suvarna Fadnavis, Rebecca R. Buchholz, Benjamin Gaubert, Néstor Y. Rojas, Thiago Nogueira, Thérèse Salameh, and Min Huang
Atmos. Chem. Phys., 24, 12225–12257, https://doi.org/10.5194/acp-24-12225-2024, https://doi.org/10.5194/acp-24-12225-2024, 2024
Short summary
Short summary
We investigated tropospheric ozone spatial variability and trends from 2005 to 2019 and related those to ozone precursors on global and regional scales. We also investigate the spatiotemporal characteristics of the ozone formation regime in relation to ozone chemical sources and sinks. Our analysis is based on remote sensing products of the tropospheric column of ozone and its precursors, nitrogen dioxide, formaldehyde, and total column CO, as well as ozonesonde data and model simulations.
Ragnhild Bieltvedt Skeie, Marit Sandstad, Srinath Krishnan, Gunnar Myhre, and Maria Sand
EGUsphere, https://doi.org/10.5194/egusphere-2024-3079, https://doi.org/10.5194/egusphere-2024-3079, 2024
Short summary
Short summary
Hydrogen leakages can alter the amount of climate gases in the atmosphere and hence have a climate impact. In this study we investigate, using an atmospheric chemistry model, how this indirect climate effect differs for different amounts of leakages, where the hydrogen leaks and if this effect changes in the future. The effect is largest for emissions far from areas where hydrogen is removed from the atmosphere by the soil, but these are not relevant locations for a future hydrogen economy.
Mariano Mertens, Sabine Brinkop, Phoebe Graf, Volker Grewe, Johannes Hendricks, Patrick Jöckel, Anna Lanteri, Sigrun Matthes, Vanessa S. Rieger, Mattia Righi, and Robin N. Thor
Atmos. Chem. Phys., 24, 12079–12106, https://doi.org/10.5194/acp-24-12079-2024, https://doi.org/10.5194/acp-24-12079-2024, 2024
Short summary
Short summary
We quantified the contributions of land transport, shipping, and aviation emissions to tropospheric ozone; its radiative forcing; and the reductions of the methane lifetime using chemistry-climate model simulations. The contributions were analysed for the conditions of 2015 and for three projections for the year 2050. The results highlight the challenges of mitigating ozone formed by emissions of the transport sector, caused by the non-linearitiy of the ozone chemistry and the long lifetime.
Jincheol Park, Yunsoo Choi, and Sagun Kayastha
EGUsphere, https://doi.org/10.5194/egusphere-2024-3312, https://doi.org/10.5194/egusphere-2024-3312, 2024
Short summary
Short summary
We investigated NOx emissions’ contributions to nitrogen loadings across five regions of East Asia during the 2022 winter-spring transition through chemical transport modeling informed by satellite data. As seasons progress, local contributions within each region to its NOy budget decreased from 32 %–43 % to 23 %–30 %, while transboundary contributions increased from 16 %–33 % to 27 %–37 %, driven by a shift in synoptic settings that allowed pollutants to spread more broadly across the regions.
Lauri Franzon, Marie Camredon, Richard Valorso, Bernard Aumont, and Theo Kurtén
Atmos. Chem. Phys., 24, 11679–11699, https://doi.org/10.5194/acp-24-11679-2024, https://doi.org/10.5194/acp-24-11679-2024, 2024
Short summary
Short summary
In this article we investigate the formation of large, sticky molecules from various organic compounds entering the atmosphere as primary emissions and the degree to which these processes may contribute to organic aerosol particle mass. More specifically, we qualitatively investigate a recently discovered chemical reaction channel for one of the most important short-lived radical compounds, peroxy radicals, and discover which of these reactions are most atmospherically important.
Siting Li, Yiming Liu, Yuqi Zhu, Yinbao Jin, Yingying Hong, Ao Shen, Yifei Xu, Haofan Wang, Haichao Wang, Xiao Lu, Shaojia Fan, and Qi Fan
Atmos. Chem. Phys., 24, 11521–11544, https://doi.org/10.5194/acp-24-11521-2024, https://doi.org/10.5194/acp-24-11521-2024, 2024
Short summary
Short summary
This study establishes an inventory of anthropogenic chlorine emissions in China in 2019 with expanded species (HCl, Cl-, Cl2, HOCl) and sources (41 specific sources). The inventory is validated by a modeling study against the observations. This study enhances the understanding of anthropogenic chlorine emissions in the atmosphere, identifies key sources, and provides scientific support for pollution control and climate change.
Willem E. van Caspel, Zbigniew Klimont, Chris Heyes, and Hilde Fagerli
Atmos. Chem. Phys., 24, 11545–11563, https://doi.org/10.5194/acp-24-11545-2024, https://doi.org/10.5194/acp-24-11545-2024, 2024
Short summary
Short summary
Methane in the atmosphere contributes to the production of ozone gas – an air pollutant and greenhouse gas. Our results highlight that simultaneous reductions in methane emissions help avoid offsetting the air pollution benefits already achieved by the already-approved precursor emission reductions by 2050 in the European Monitoring and Evaluation Programme region, while also playing an important role in bringing air pollution further down towards World Health Organization guideline limits.
Laura Stecher, Franziska Winterstein, Patrick Jöckel, Michael Ponater, Mariano Mertens, and Martin Dameris
EGUsphere, https://doi.org/10.5194/egusphere-2024-2938, https://doi.org/10.5194/egusphere-2024-2938, 2024
Short summary
Short summary
Methane, the second most important anthropogenic greenhouse gas, is chemically decomposed in the atmosphere. The chemical sink of atmospheric methane is not constant, but depends on the temperature and on the abundance of its reaction partners. In this study, we use a global chemistry-climate model to assess the feedback of atmospheric methane induced by changes of the chemical sink in a warming climate, and its implications for the chemical composition and the surface air temperature change.
Beata Opacka, Trissevgeni Stavrakou, Jean-François Müller, Isabelle De Smedt, Jos van Geffen, Eloise A. Marais, Rebekah P. Horner, Dylan B. Millet, Kelly C. Wells, and Alex B. Guenther
EGUsphere, https://doi.org/10.5194/egusphere-2024-2912, https://doi.org/10.5194/egusphere-2024-2912, 2024
Short summary
Short summary
Vegetation releases biogenic volatile organic compounds, while soils and lightning contribute to the natural emissions of nitrogen oxides into the atmosphere. These gases interact in complex ways. Using satellite data and models, we developed a new method to simultaneously optimise these natural emissions over Africa in 2019. Our approach led to an increase in natural emissions that is supported by independent data showing that current estimates are underestimated.
Tia R. Scarpelli, Paul I. Palmer, Mark Lunt, Ingrid Super, and Arjan Droste
Atmos. Chem. Phys., 24, 10773–10791, https://doi.org/10.5194/acp-24-10773-2024, https://doi.org/10.5194/acp-24-10773-2024, 2024
Short summary
Short summary
Under the Paris Agreement, countries must track their anthropogenic greenhouse gas emissions. This study describes a method to determine self-consistent estimates for combustion emissions and natural fluxes of CO2 from atmospheric data. We report consistent estimates inferred using this approach from satellite data and ground-based data over Europe, suggesting that satellite data can be used to determine national anthropogenic CO2 emissions for countries where ground-based CO2 data are absent.
Yufen Wang, Ke Li, Xi Chen, Zhenjiang Yang, Minglong Tang, Pascoal M. D. Campos, Yang Yang, Xu Yue, and Hong Liao
EGUsphere, https://doi.org/10.5194/egusphere-2024-2576, https://doi.org/10.5194/egusphere-2024-2576, 2024
Short summary
Short summary
The impact of biomass burning and anthropogenic emissions on high tropospheric ozone was not well studied in Southern Africa. We combined the model simulation with recent observations at the surface and from space to quantify tropospheric ozone and its main drivers in Southern Africa. Our work focuses on the impact of emissions from different sources at different spatial scales, contributing to a comprehensive understanding of air pollution drivers and their uncertainties in Southern Africa.
Wenbin Kou, Yang Gao, Dan Tong, Xiaojie Guo, Xiadong An, Wenyu Liu, Mengshi Cui, Xiuwen Guo, Shaoqing Zhang, Huiwang Gao, and Lixin Wu
EGUsphere, https://doi.org/10.5194/egusphere-2024-2500, https://doi.org/10.5194/egusphere-2024-2500, 2024
Short summary
Short summary
Unlike traditional numerical studies, we apply a high-resolution Earth system model, improving simulations of ozone and large-scale circulations such as atmospheric blocking. In addition to local heatwave effects, we quantify the impact of atmospheric blocking on downstream ozone concentrations, which is closely associated with the blocking position. We identify three major pathways of Rossby wave propagation, stressing the critical role of large-scale circulation play in regional air quality.
Qianqian Zhang, K. Folkert Boersma, Chiel van der Laan, Alba Mols, Bin Zhao, Shengyue Li, and Yuepeng Pan
EGUsphere, https://doi.org/10.5194/egusphere-2024-2641, https://doi.org/10.5194/egusphere-2024-2641, 2024
Short summary
Short summary
Accurate NOx emission estimates are required to better understand air pollution. This study investigates and demonstrates the ability of the superposition column model in combination with TROPOMI tropospheric NO2 column data to estimate city-scale NOx emissions and lifetimes and their variabilities. The results of this work nevertheless confirm the strength of the superposition column model in estimating urban NOx emissions with reasonable accuracy.
Ryan J. Pound, Lucy V. Brown, Mat J. Evans, and Lucy J. Carpenter
Atmos. Chem. Phys., 24, 9899–9921, https://doi.org/10.5194/acp-24-9899-2024, https://doi.org/10.5194/acp-24-9899-2024, 2024
Short summary
Short summary
Iodine-mediated loss of ozone to the ocean surface and the subsequent emission of iodine species has a large effect on the troposphere. Here we combine recent experimental insights to develop a box model of the process, which we then parameterize and incorporate into the GEOS-Chem transport model. We find that these new insights have a small impact on the total emission of iodine but significantly change its distribution.
Mingzhao Liu, Lars Hoffmann, Jens-Uwe Grooß, Zhongyin Cai, Sabine Grießbach, and Yi Heng
EGUsphere, https://doi.org/10.5194/egusphere-2024-2596, https://doi.org/10.5194/egusphere-2024-2596, 2024
Short summary
Short summary
We studied the transport and chemical decomposition of volcanic SO2, focusing on the 2019 Raikoke event. By comparing two different chemistry modeling schemes, we found that including complex chemical reactions leads to a more accurate prediction of how long SO2 stays in the atmosphere. This research helps improve our understanding of volcanic pollution and its impact on air quality and climate, providing better tools for scientists to track and predict the movement of these pollutants.
Alok K. Pandey, David S. Stevenson, Alcide Zhao, Richard J. Pope, Ryan Hossaini, Krishan Kumar, and Marytn P. Chipperfield
EGUsphere, https://doi.org/10.5194/egusphere-2024-2686, https://doi.org/10.5194/egusphere-2024-2686, 2024
Short summary
Short summary
Nitrogen dioxide is an air pollutant largely controlled by human activity that affects ozone, methane and aerosols. Satellite instruments can quantify column NO2, and by carefully matching the time and location of measurements, enable evaluation of model simulations. NO2 over SE Asia is assessed, showing that the model captures many features of the measurements, but also important differences that suggest model deficiencies in representing several aspects of the atmospheric chemistry of NO2.
Katherine R. Travis, Benjamin A. Nault, James H. Crawford, Kelvin H. Bates, Donald R. Blake, Ronald C. Cohen, Alan Fried, Samuel R. Hall, L. Gregory Huey, Young Ro Lee, Simone Meinardi, Kyung-Eun Min, Isobel J. Simpson, and Kirk Ullman
Atmos. Chem. Phys., 24, 9555–9572, https://doi.org/10.5194/acp-24-9555-2024, https://doi.org/10.5194/acp-24-9555-2024, 2024
Short summary
Short summary
Human activities result in the emission of volatile organic compounds (VOCs) that contribute to air pollution. Detailed VOC measurements were taken during a field study in South Korea. When compared to VOC inventories, large discrepancies showed underestimates from chemical products, liquefied petroleum gas, and long-range transport. Improved emissions and chemistry of these VOCs better described urban pollution. The new chemical scheme is relevant to urban areas and other VOC sources.
Beth S. Nelson, Zhenze Liu, Freya A. Squires, Marvin Shaw, James R. Hopkins, Jacqueline F. Hamilton, Andrew R. Rickard, Alastair C. Lewis, Zongbo Shi, and James D. Lee
Atmos. Chem. Phys., 24, 9031–9044, https://doi.org/10.5194/acp-24-9031-2024, https://doi.org/10.5194/acp-24-9031-2024, 2024
Short summary
Short summary
The impact of combined air quality and carbon neutrality policies on O3 formation in Beijing was investigated. Emissions inventory data were used to estimate future pollutant mixing ratios relative to ground-level observations. O3 production was found to be most sensitive to changes in alkenes, but large reductions in less reactive compounds led to larger reductions in future O3 production. This study highlights the importance of understanding the emissions of organic pollutants.
Amir H. Souri, Bryan N. Duncan, Sarah A. Strode, Daniel C. Anderson, Michael E. Manyin, Junhua Liu, Luke D. Oman, Zhen Zhang, and Brad Weir
Atmos. Chem. Phys., 24, 8677–8701, https://doi.org/10.5194/acp-24-8677-2024, https://doi.org/10.5194/acp-24-8677-2024, 2024
Short summary
Short summary
We explore a new method of using the wealth of information obtained from satellite observations of Aura OMI NO2, HCHO, and MERRA-2 reanalysis in NASA’s GEOS model equipped with an efficient tropospheric OH (TOH) estimator to enhance the representation of TOH spatial distribution and its long-term trends. This new framework helps us pinpoint regional inaccuracies in TOH and differentiate between established prior knowledge and newly acquired information from satellites on TOH trends.
Haipeng Lin, Louisa K. Emmons, Elizabeth W. Lundgren, Laura Hyesung Yang, Xu Feng, Ruijun Dang, Shixian Zhai, Yunxiao Tang, Makoto M. Kelp, Nadia K. Colombi, Sebastian D. Eastham, Thibaud M. Fritz, and Daniel J. Jacob
Atmos. Chem. Phys., 24, 8607–8624, https://doi.org/10.5194/acp-24-8607-2024, https://doi.org/10.5194/acp-24-8607-2024, 2024
Short summary
Short summary
Tropospheric ozone is a major air pollutant, a greenhouse gas, and a major indicator of model skill. Global atmospheric chemistry models show large differences in simulations of tropospheric ozone, but isolating sources of differences is complicated by different model environments. By implementing the GEOS-Chem model side by side to CAM-chem within a common Earth system model, we identify and evaluate specific differences between the two models and their impacts on key chemical species.
Victor Lannuque and Karine Sartelet
Atmos. Chem. Phys., 24, 8589–8606, https://doi.org/10.5194/acp-24-8589-2024, https://doi.org/10.5194/acp-24-8589-2024, 2024
Short summary
Short summary
Large uncertainties remain in understanding secondary organic aerosol (SOA) formation and speciation from naphthalene oxidation. This study details the development of the first near-explicit chemical scheme for naphthalene oxidation by OH, which includes kinetic and mechanistic data, and is able to reproduce most of the experimentally identified products in both gas and particle phases.
Cited articles
Abbott, M. L., Lin, C.-J., Martian, P., and Einerson, J. J.: Atmospheric mercury near Salmon Falls Creek Reservoir in southern Idaho, Appl. Geochem., 23, 438–453, 2008.
Akhtar, U. S.: Atmospheric total gaseous mercury concentration measurement in Windsor: A study of variability and potential sources, MASc Thesis, University of Windsor, Windsor, Ontario, Canada, 2008.
Belis, C. A., Karagulian, F., Larsen, B. R., and Hopke, P. K.: Critical review and meta-analysis of ambient particulate matter source apportionment using receptor models in Europe, Atmos. Environ., 69, 94–108, 2013.
Blanchard, P., Froude, F. A., Martin, J. B., Dryfhout-Clark, H., and Woods, J. T.: Four years of continuous total gaseous mercury (TGM) measurements at sites in Ontario, Canada, Atmos. Environ., 36, 3735–3743, 2002.
Chen, L. W. A., Watson, J. G., Chow, J. C., DuBois, D. W., and Herschberger, L.: PM2.5 source apportionment: reconciling receptor models for US nonurban and urban long-term networks, JAPCA J. Air Waste Ma., 61, 1204–1217, 2011.
Cheng, I., Lu, J., and Song, X.: Studies of Potential Sources that Contributed to Atmospheric Mercury in Toronto, Canada, Atmos. Environ., 43, 6145–6158, 2009.
Cheng, I., Zhang, L., Blanchard, P., Graydon, J. A., and Louis, V. L. St.: Source-receptor relationships for speciated atmospheric mercury at the remote Experimental Lakes Area, northwestern Ontario, Canada, Atmos. Chem. Phys., 12, 1903–1922, https://doi.org/10.5194/acp-12-1903-2012, 2012.
Cheng, I., Zhang, L., Blanchard, P., Dalziel, J., Tordon, R., Huang, J., and Holsen, T. M.: Comparisons of mercury sources and atmospheric mercury processes between a coastal and inland site, J. Geophys. Res.-Atmos., 118, 2434–2443, 2013a.
Cheng, I., Zhang, L., Blanchard, P., Dalziel, J., and Tordon, R.: Concentration-weighted trajectory approach to identifying potential sources of speciated atmospheric mercury at an urban coastal site in Nova Scotia, Canada, Atmos. Chem. Phys., 13, 6031–6048, https://doi.org/10.5194/acp-13-6031-2013, 2013b.
Choi, H.-D., Holsen, T. M., and Hopke, P. K.: Atmospheric Mercury (Hg) in the Adirondacks: Concentrations and Sources, Environ. Sci. Technol., 42, 5644–5653, 2008.
de Foy, B., Wiedinmyer, C., and Schauer, J. J.: Estimation of mercury emissions from forest fires, lakes, regional and local sources using measurements in Milwaukee and an inverse method, Atmos. Chem. Phys., 12, 8993–9011, https://doi.org/10.5194/acp-12-8993-2012, 2012.
Draxler, R. R. and Rolph, G. D.: HYSPLIT (HYbrid Single-Particle Lagrangian Integrated Trajectory), NOAA Air Resources Laboratory, College Park, MD, available at: http://www.arl.noaa.gov/HYSPLIT.php (last access: 20 February 2015), 2014.
Ebinghaus, R., Slemr, F., Brenninkmeijer, C. A. M., Van Velthoven, P., Zahn, A., Hermann, M., O'Sullivan, D. A., and Oram, D. E.: Emissions of gaseous mercury from biomass burning in South America in 2005 observed during CARIBIC flights, Geophys. Res. Lett., 34, L08813, https://doi.org/10.1029/2006GL028866, 2007.
Eckley, C. S. and Branfireun, B.: Gaseous mercury emissions from urban surfaces: controls and spatiotemporal trends, Appl. Geochem., 23, 369–383, 2008.
Eckley, C. S., Parsons, M. T., Mintz, R., Lapalme, M., Mazur, M., Tordon, R., Elleman, R., Graydon, J. A., Blanchard, P., and St. Louis, V.: Impact of closing Canada's largest point-source of mercury emissions on local atmospheric mercury concentrations, Environ. Sci. Technol., 47, 10339–10348, 2013.
Fa\"in, X., Obrist, D., Hallar, A. G., Mccubbin, I., and Rahn, T.: High levels of reactive gaseous mercury observed at a high elevation research laboratory in the Rocky Mountains, Atmos. Chem. Phys., 9, 8049–8060, https://doi.org/10.5194/acp-9-8049-2009, 2009.
Fast, J. D. and Easter, R.: A Lagrangian Particle Dispersion Model Compatible with WRF, in: 7th WRF User's Workshop, Boulder, CO, USA, 2006.
Fu, X., Feng, X., Qiu, G., Shang, L., and Zhang, H.: Speciated atmospheric mercury and its potential source in Guiyang, China, Atmos. Environ., 45, 4205–4212, 2011.
Fu, X. W., Feng, X., Liang, P., Deliger, Zhang, H., Ji, J., and Liu, P.: Temporal trend and sources of speciated atmospheric mercury at Waliguan GAW station, Northwestern China, Atmos. Chem. Phys., 12, 1951–1964, https://doi.org/10.5194/acp-12-1951-2012, 2012a.
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, 2012b.
Gao, F.: A comprehensive investigation of ambient Mercury in the Ohio River valley: source-receptor relationship and meteorological impact, Doctoral dissertation, Ohio University, Athens, Ohio, United States, 2007.
Graney, J. R., Dvonch, J. T., and Keeler, G. J.: Use of multi-element tracers to source apportion mercury in south Florida aerosols, Atmos. Environ., 38, 1715–1726, 2004.
Gustin, M. S., Weiss-Penzias, P. S., and Peterson, C.: Investigating sources of gaseous oxidized mercury in dry deposition at three sites across Florida, USA, Atmos. Chem. Phys., 12, 9201–9219, https://doi.org/10.5194/acp-12-9201-2012, 2012.
Gustin, M. S., Amos, H. M., Huang, J., Miller, M. B., and Heidecorn, K.: Measuring and modeling mercury in the atmosphere: a critical review, Atmos. Chem. Phys., 15, 5697–5713, https://doi.org/10.5194/acp-15-5697-2015, 2015.
Han, Y.-J., Holsen, T. M., Lai, S.-O., Hopke, P. K., Yi, S.-M., Liu, W., Pagano, J., Falanga, L., Milligan, M., and Andolina, C.: Atmospheric gaseous mercury concentrations in New York State: relationships with meteorological data and other pollutants, Atmos. Environ., 38, 6431–6446, 2004.
Han, Y.-J., Holsen, T. M., Hopke, P. K., and Yi, S.-M.: Comparison between Back-Trajectory Based Modeling and Lagrangian Backward Dispersion Modeling for Locating Sources of Reactive Gaseous Mercury, Environ. Sci. Technol., 39, 1715–1723, 2005.
Han, Y. J., Holsen, T. M., and Hopke, P. K.: Estimation of source locations of total gaseous mercury measured in New York State using trajectory-based models, Atmos. Environ., 41, 6033–6047, 2007.
Hegarty, J., Mao, H., and Talbot, R.: Synoptic influences on springtime tropospheric O3 and CO over the North American export region observed by TES, Atmos. Chem. Phys., 9, 3755–3776, https://doi.org/10.5194/acp-9-3755-2009, 2009.
Hegarty, J., Draxler, R. R., Stein, A. F., Brioude, J., Mountain, M., Eluszkiewicz, J., Nehrkorn, T., Ngan, F., and Andrews, A.: Evaluation of Lagrangian particle dispersion models with measurements from controlled tracer releases, J. Appl. Meteorol. Climatol., 52, 2623–2637, 2013.
Holmes, C. D., Jacob, D. J., and Yang, X.: Global lifetime of elemental mercury against oxidation by atomic bromine in the free troposphere, Geophys. Res. Lett., 33, L20808, https://doi.org/10.1029/2006GL027176, 2006.
Holmes, C. D., Jacob, D. J., Mason, R. P., and Jaffe, D. A.: Sources and deposition of reactive gaseous mercury in the marine atmosphere, Atmos. Environ., 43, 2278–2285, 2009.
Hopke, P. K.: Recent developments in receptor modeling, J. Chemometr., 17, 255–265, 2003.
Hopke, P. K.: The Use of Source Apportionment for Air Quality Management and Health Assessments, J. Toxicol. Env. Heal. A, 71, 555–563, 2008.
Hopke, P. K. and Cohen, D. D.: Application of receptor modeling methods, Atmos. Pollut. Res., 2, 122–125, 2011.
Hopke, P. K., Ito, K., Mar, T., Christensen, W. F., Eatough, D. J., Henry, R. C., Kim, E., Laden, F., Lall, R., Larson, T. V., Liu, H., Neas, L., Pinto, J., Stölzel, M., Suh, H., Paatero, P., and Thurston, G. D.: PM source apportionment and health effects: 1. Intercomparison of source apportionment results, J. Expo. Sci. Environ. Epidemiol., 16, 275–286, 2005.
Huang, J., Choi, H.-D., Hopke, P. K., and Holsen, T. M.: Ambient Mercury Sources in Rochester, NY: Results from Principle Components Analysis (PCA) of Mercury Monitoring Network Data, Environ. Sci. Technol., 44, 8441–8445, 2010.
Jeong, U., Kim, J., Lee, H., Jung, J., Kim, Y. J., Song, C. H., and Koo, J.-H.: Estimation of the contributions of long range transported aerosol in East Asia to carbonaceous aerosol and PM concentrations in Seoul, Korea using highly time resolved measurements: a PSCF model approach, J. Environ. Monitor., 13, 1905–1918, https://doi.org/10.1039/c0em00659a, 2011.
Kabashnikov, V. P., Chaikovsky, A. P., Kucsera, T. L., and Metelskaya, N. S.: Estimated accuracy of three common trajectory statistical methods, Atmos. Environ., 45, 5425–5430, 2011.
Keeler, G. J., Landis, M. S., Norris, G. A., Christianson, E. M., and Dvonch, J. T.: Sources of mercury wet deposition in Eastern Ohio, USA, Environ. Sci. Technol., 40, 5874–5881, 2006.
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, K. H., Shon, Z. H., Nguyen, H. T., Jung, K., Park, C. G., and Bae, G. N.: The effect of man made source processes on the behavior of total gaseous mercury in air: A comparison between four urban monitoring sites in Seoul Korea, Sci. Total Environ., 409, 3801–3811, 2011.
Kolker, A., Olson, M. L., Krabbenhoft, D. P., Tate, M. T., and Engle, M. A.: Patterns of mercury dispersion from local and regional emission sources, rural Central Wisconsin, USA, Atmos. Chem. Phys., 10, 4467–4476, https://doi.org/10.5194/acp-10-4467-2010, 2010.
Lalonde, J. D., Amyot, M., Doyon, M. R., and Auclair, J. C.: Photo-induced Hg (II) reduction in snow from the remote and temperate Experimental Lakes Area (Ontario, Canada), J. Geophys. Res., 108, 4200, https://doi.org/10.1029/2001JD001534, 2003.
Landis, M. S., Lewis, C. W., Stevens, R. K., Keeler, G. J., Dvonch, J. T., and Tremblay, R. T.: Ft. McHenry tunnel study: Source profiles and mercury emissions from diesel and gasoline powered vehicles, Atmos. Environ., 41, 8711–8724, 2007.
Laurier, F. J. G., Mason, R. P., Whalin, L., and Kato, S.: Reactive gaseous mercury formation in the North Pacific Ocean's marine boundary layer: A potential role of halogen chemistry, J. Geophys. Res., 108, 4529, https://doi.org/10.1029/2003JD003625, 2003.
Lee, G. S., Kim, P. R., Han, Y. J., Holsen, T. M., and Lee, S. H.: Tracing Sources of Total Gaseous Mercury to Yongheung Island off the Coast of Korea, Atmosphere, 5, 273–291, 2014.
Lee, J. H. and Hopke, P. K.: Apportioning sources of PM2.5 in St. Louis, MO using speciation trends network data, Atmos. Environ., 40, S360–S377, 2006.
Lee, S., Liu, W., Wang, Y., Russell, A. G., and Edgerton, E. S.: Source apportionment of PM2.5: Comparing PMF and CMB results for four ambient monitoring sites in the southeastern United States, Atmos. Environ., 42, 4126–4137, 2008.
Li, J., Sommar, J., Wängberg, I., Lindqvist, O., and Wei, S.-Q.: Short-time variation of mercury speciation in the urban of Göteborg during GÖTE-2005, Atmos. Environ., 42, 8382–8388, 2008.
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, W., Hopke, P. K., Han, Y. J., Yi, S. M., Holsen, T. M., Cybart, S., Kozlowski, K., and Milligan, M.: Application of receptor modeling to atmospheric constituents at Potsdam and Stockton, NY, Atmos. Environ., 37, 4997–5007, 2003.
Lyman, S. N. and Gustin, M. S.: Speciation of atmospheric mercury at two sites in northern Nevada, USA, Atmos. Environ., 42, 927–939, 2008.
Lyman, S. N. and Jaffe, D. A.: Formation and fate of oxidized mercury in the upper troposphere and lower stratosphere, Nature Geosci., 5, 114–117, 2012.
Lynam, M. M. and Keeler, G. J.: Automated speciated mercury measurements in Michigan, Environ. Sci. Technol., 39, 9253–9262, 2005.
Lynam, M. M. and Keeler, G. J.: Source–receptor relationships for atmospheric mercury in urban Detroit, Michigan, Atmos. Environ., 40, 3144–3155, 2006.
Majewski, G., Czechowski, P. O., Badyda, A. J., and Rogula-Kozłowska, W.: The Estimation of Total Gaseous Mercury Concentration (TGM) Using Exploratory and Stochastic Methods, Pol. J. Environ. Stud., 22, 759–771, 2013.
Murphy, D. M., Hudson, P. K., Thomson, D. S., Sheridan, P. J., and Wilson, J. C.: Observations of mercury-containing aerosols, Environ. Sci. Technol., 40, 3163–3167, 2006.
Paatero, P. and Tapper, U.: Positive Matrix Factorization: a Non-Negative Factor Model with Optimal Utilization of Error Estimates of Data Values, Envirometrics, 5, 111–126, 1994.
Pant, P. and Harrison, R. M.: Critical review of receptor modelling for particulate matter: a case study of India, Atmos. Environ., 49, 1–12, 2012.
Parsons, M. T., McLennan, D., Lapalme, M., Mooney, C., Watt, C., and Mintz, R.: Total Gaseous Mercury Concentration Measurements at Fort McMurray, Alberta, Canada, Atmosphere, 4, 472–493, 2013.
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.
Pirrone, N., Cinnirella, S., Feng, X., Finkelman, R. B., Friedli, H. R., Leaner, J., Mason, R., Mukherjee, A. B., Stracher, G. B., Streets, D. G., and Telmer, K.: Global mercury emissions to the atmosphere from anthropogenic and natural sources, Atmos. Chem. Phys., 10, 5951–5964, https://doi.org/10.5194/acp-10-5951-2010, 2010.
Reff, A., Eberly, S. I., and Bhave, P. V.: Receptor modeling of ambient particulate matter data using positive matrix factorization: review of existing methods, JAPCA J. Air Waste Ma., 57, 146–154, 2007.
Ren, X., Luke, W. T., Kelley, P., Cohen, M., Ngan, F., Artz, R., Walker, J., Brooks, S., Moore, C., Swartzendruber, P., Bauer, D., Remeika, J., Hynes, A., Dibb, J., Rolison, J., Krishnamurthy, N., Landing, W. M., Hecobian, A., Shook, J., and Huey, L. G.: Mercury Speciation at a Coastal Site in the Northern Gulf of Mexico: Results from the Grand Bay Intensive Studies in Summer 2010 and Spring 2011, Atmosphere, 5, 230–251, 2014.
Rolph, G. D.: Real-time Environmental Applications and Display sYstem (READY) Website, NOAA Air Resources Laboratory, College Park, MD, available at: http://www.ready.noaa.gov (last access: 20 February 2015), 2014.
Rutter, A. P., Schauer, J. J., Lough, G. C., Snyder, D. C., Kolb, C. J., Klooster, S. V., Rudolf, T., Manolopoulos, H., and Olson, M. L.: A comparison of speciated atmospheric mercury at an urban center and an upwind rural location, J. Environ. Monitor., 10, 102–108, 2007.
Rutter, A. P., Snyder, D. C., Stone, E. A., Schauer, J. J., Gonzalez-Abraham, R., Molina, L. T., Márquez, C., Cárdenas, B., and de Foy, B.: In situ measurements of speciated atmospheric mercury and the identification of source regions in the Mexico City Metropolitan Area, Atmos. Chem. Phys., 9, 207–220, https://doi.org/10.5194/acp-9-207-2009, 2009.
Schroeder, W. H. and Munthe, J.: Atmospheric mercury – an overview, Atmos. Environ., 32, 809–822, 1998.
Selin, N. E. and Jacob, D. J.: Seasonal and spatial patterns of mercury wet deposition in the United States: Constraints on the contribution from North American anthropogenic sources, Atmos. Environ., 42, 5193–5204, 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., Weigelt, A., Ebinghaus, R., Brenninkmeijer, C., Baker, A., Schuck, T., Rauthe-Schöch, A., Leedham, E., Hermann, M., van Velthoven, P., Oram, D., O'Sullivan D., Dyroff, C., Zahn, A., and Ziereis, H.: Mercury plumes in the global upper troposphere observed during flights with the CARIBIC Observatory from May 2005 until June 2013, Atmosphere, 5, 342–369, 2014.
Song, Y., Dai, W., Shao, M., Liu, Y., Lu, S., Kuster, W., and Goldan, P.: Comparison of receptor models for source apportionment of volatile organic compounds in Beijing, China, Environ. Pollut., 156, 174–183, 2008.
Sprovieri, F. and Pirrone, N.: Spatial and temporal distribution of atmospheric mercury species over the Adriatic Sea, Environ. Fluid Mech., 8, 117–128, 2008.
Stohl, A.: Trajectory statistics-a new method to establish source-receptor relationships of air pollutants and its application to the transport of particulate sulfate in Europe, Atmos. Environ., 30, 579–587, 1996.
Stohl, A.: Computation, accuracy and applications of trajectories-a review and bibliography, Atmos. Environ., 32, 947–966, 1998.
Stohl, A., Forster, C., Frank, A., Seibert, P., and Wotawa, G.: Technical note: The Lagrangian particle dispersion model FLEXPART version 6.2, Atmos. Chem. Phys., 5, 2461–2474, https://doi.org/10.5194/acp-5-2461-2005, 2005.
Subir, M., Ariya, P. A., and Dastoor, A. P.: A review of the sources of uncertainties in atmospheric mercury modeling II. Mercury surface and heterogeneous chemistry – A missing link, Atmos. Environ., 46, 1–10, https://doi.org/10.1016/j.atmosenv.2011.07.047, 2012.
Swartzendruber, P. C.: The distribution and speciation of mercury in the free troposphere of the Pacific northwest, Doctoral dissertation, University of Washington, Seattle, Washington, USA, 2006.
Swartzendruber, P. C., Jaffe, D. A., Prestbo, E. M., Weiss-Penzias, P., Selin, N. E., Park, R., Jacob, D., Strode, S., and Jaeglé, L.: Observations of reactive gaseous mercury in the free-troposphere at the Mt. Bachelor observatory, J. Geophys. Res., 111, D24301, https://doi.org/10.1029/2006JD007415, 2006.
Tauler, R., Viana, M., Querol, X., Alastuey, A., Flight, R. M., Wentzell, P. D., and Hopke, P. K.: Comparison of the results obtained by four receptor modelling methods in aerosol source apportionment studies, Atmos. Environ., 43, 3989–3997, 2009.
Temme, C., Blanchard, P., Steffen, A., Banic, C., Beauchamp, S., Poissant, L., Tordon, R., and Wiens, B.: Trend, seasonal and multivariate analysis study of total gaseous mercury data from the Canadian atmospheric mercury measurement network (CAMNet), Atmos. Environ., 41, 5423–5441, 2007.
Thurston, G. D. and Spengler, J. D.: A quantitative assessment of source contributions to inhalable particulate matter pollution in metropolitan Boston, Atmos. Environ., 19, 9–25, 1985.
Timonen, H., Ambrose, J. L., and Jaffe, D. A.: Oxidation of elemental Hg in anthropogenic and marine airmasses, Atmos. Chem. Phys., 13, 2827–2836, https://doi.org/10.5194/acp-13-2827-2013, 2013.
Travnikov, O., Lin, C.-J., Dastoor, A., Bullock, O. R., Hedgecock, I. M., Holmes, C., Ilyin, I., Jaeglé, L., Jung, G., Pan, L., Pongprueksa, P., Ryzhkov, A., Seigneur, C., and Skov, H.: Global and Regional Modelling, in: United Nations Economic Commission for Europe, Hemispheric Transport of Air Pollution 2010, Part B: Mercury, Air Pollution Studies No. 18, edited by: Pirrone, N. and Keating, T., ISSN 1014-4625, United Nations Publication, Geneva, Chap. 4, 97–144, 2010.
USEPA: Technology Transfer Network Clearinghouse for Inventories & Emissions Factors: SPECIATE Version 4.3, available at: http://www.epa.gov/ttn/chief/software/speciate/index.html#speciate (last access: 20 February 2015), 2014a.
USEPA: EPA Positive Matrix Factorization (PMF) 5.0 Fundamentals and User Guide, available at: http://www.epa.gov/heasd/research/pmf.html (last access: 20 February 2015), 2014b.
Viana, M., Kuhlbusch, T. A. J., Querol, X., Alastuey, A., Harrison, R. M., Hopke, P. K., Winiwarter, W., Vallius, M., Szidat, S., Prévôt, A. S. H., Hueglin, C., Bloemen, H., Wåhlin, P., Vecchi, R., Miranda, A. I., Kasper-Giebl, A., Maenhaut, W., and Hitzenberger, R.: Source apportionment of particulate matter in Europe: a review of methods and results, J. Aerosol. Sci., 39, 827–849, 2008a.
Viana, M., Pandolfi, M., Minguillón, M. C., Querol, X., Alastuey, A., Monfort, E., and Celades, I.: Inter-comparison of receptor models for PM source apportionment: case study in an industrial area, Atmos. Environ., 42, 3820–3832, 2008b.
Wan, Q., Feng, X., Lu, J., Zheng, W., Song, X., Han, S., and Xu, H.: Atmospheric mercury in Changbai Mountain area, northeastern China I. The seasonal distribution pattern of total gaseous mercury and its potential sources, Environ. Res., 109, 201–206, 2009a.
Wan, Q., Feng, X., Lu, J., Zheng, W., Song, X., Han, S., and Xu, H.: Atmospheric mercury in Changbai Mountain area, northeastern China II. The distribution of reactive gaseous mercury and particulate mercury and mercury deposition fluxes, Environ. Res., 109, 721–727, 2009b.
Wang, Y., Huang, J., Hopke, P. K., Rattigan, O. V., Chalupa, D. C., Utell, M. J., and Holsen, T. M.: Effect of the shutdown of a large coal-fired power plant on ambient mercury species, Chemosphere, 92, 360–367, 2013.
Watson, J. G., Chen, L. W. A., Chow, J. C., Doraiswamy, P., and Lowenthal, D. H.: Source Apportionment: Findings from the U.S. Supersites Program, JAPCA J. Air Waste Ma., 58, 265–288, https://doi.org/10.3155/1047-3289.58.2.265, 2008.
Weiss-Penzias, P., Jaffe, D., 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 Mount Bachelor Observatory, Atmos. Environ., 41, 4366–4379, 2007.
Weiss-Penzias, P., Gustin, M. S., and Lyman, S. N.: Observations of speciated atmospheric mercury at three sites in Nevada, USA: evidence for a free tropospheric source of reactive gaseous mercury, J. Geophys. Res., 114, D14302, https://doi.org/10.1029/2008JD011607, 2009.
Weiss-Penzias, P. S., Gustin, M. S., and Lyman, S. N.: Sources of gaseous oxidized mercury and mercury dry deposition at two southeastern U.S. sites, Atmos. Environ., 45, 4569–4579, https://doi.org/10.1016/j.atmosenv.2011.05.069, 2011.
Xu, L., Chen, J., Yang, L., Niu, Z., Tong, L., Yin, L., and Chen, Y.: Characteristics and sources of atmospheric mercury speciation in a coastal city, Xiamen, China, Chemosphere, 119, 530–539, 2015.
Xu, X. and Akhtar, U. S.: Identification of potential regional sources of atmospheric total gaseous mercury in Windsor, Ontario, Canada using hybrid receptor modeling, Atmos. Chem. Phys., 10, 7073–7083, https://doi.org/10.5194/acp-10-7073-2010, 2010.
Xu, X., Akhtar, U., Clark, K., and Wang, X.: Temporal Variability of Atmospheric Total Gaseous Mercury in Windsor, ON, Canada, Atmosphere, 5, 536–556, 2014.
Zhang, L., Vet, R., Wiebe, A., Mihele, C., Sukloff, B., Chan, E., Moran, M. D., and Iqbal, S.: Characterization of the size-segregated water-soluble inorganic ions at eight Canadian rural sites, Atmos. Chem. Phys., 8, 7133–7151, https://doi.org/10.5194/acp-8-7133-2008, 2008.
Short summary
Current knowledge of receptor-based studies using speciated atmospheric mercury is reviewed and recommendations for future research needs are provided.
Current knowledge of receptor-based studies using speciated atmospheric mercury is reviewed and...
Altmetrics
Final-revised paper
Preprint