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DOI10.1073/pnas.1900613116
Direct detection of atmospheric atomic bromine leading to mercury and ozone depletion
Wang S.; McNamara S.M.; Moore C.W.; Obrist D.; Steffen A.; Shepson P.B.; Staebler R.M.; Raso A.R.W.; Pratt K.A.
发表日期2019
ISSN0027-8424
起始页码14479
结束页码14484
卷号116期号:29
英文摘要Bromine atoms play a central role in atmospheric reactive halogen chemistry, depleting ozone and elemental mercury, thereby enhancing deposition of toxic mercury, particularly in the Arctic near-surface troposphere. However, direct bromine atom measurements have been missing to date, due to the lack of analytical capability with sufficient sensitivity for ambient measurements. Here we present direct atmospheric bromine atom measurements, conducted in the springtime Arctic. Measured bromine atom levels reached 14 parts per trillion (ppt, pmol mol−1; 4.2 × 108 atoms per cm−3) and were up to 3–10 times higher than estimates using previous indirect measurements not considering the critical role of molecular bromine. Observed ozone and elemental mercury depletion rates are quantitatively explained by the measured bromine atoms, providing field validation of highly uncertain mercury chemistry. Following complete ozone depletion, elevated bromine concentrations are sustained by photochemical snowpack emissions of molecular bromine and nitrogen oxides, resulting in continued atmospheric mercury depletion. This study provides a breakthrough in quantitatively constraining bromine chemistry in the polar atmosphere, where this chemistry connects the rapidly changing surface to pollutant fate. © 2019 National Academy of Sciences. All rights reserved.
英文关键词Atmosphere; Bromine; Mercury; Ozone
语种英语
scopus关键词bromine; mercury; Article; chemical analysis; chemical modification; chemical reaction kinetics; concentration (parameter); ozone depletion; physical chemistry; physical parameters; priority journal; quantitative analysis; sensitivity analysis
来源期刊Proceedings of the National Academy of Sciences of the United States of America
文献类型期刊论文
条目标识符http://gcip.llas.ac.cn/handle/2XKMVOVA/160396
作者单位Wang, S., Department of Chemistry, University of Michigan, Ann Arbor, MI 48109, United States; McNamara, S.M., Department of Chemistry, University of Michigan, Ann Arbor, MI 48109, United States; Moore, C.W., Division of Atmospheric Science, Desert Research Institute, Reno, NV 89523, United States, Gas Technology Institute, Des Plaines, IL 60018, United States; Obrist, D., Division of Atmospheric Science, Desert Research Institute, Reno, NV 89523, United States, Department of Environmental, Earth and Atmospheric Sciences, University of Massachusetts, Lowell, MA 01854, United States; Steffen, A., Air Quality Processes Research Section, Environment and Climate Change Canada, Toronto, ON M3H5T4, Canada; Shepson, P.B., Department of Chemistry, Purdue University, West Lafayette, IN 47907, United States, Department of Earth, Atmospheric, and Planetary Sciences, Purdue University, West Lafayette, IN 47907, United States, Purdue Climate Change Research Center, Purdue University, West Lafayette, IN 47907...
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Wang S.,McNamara S.M.,Moore C.W.,et al. Direct detection of atmospheric atomic bromine leading to mercury and ozone depletion[J],2019,116(29).
APA Wang S..,McNamara S.M..,Moore C.W..,Obrist D..,Steffen A..,...&Pratt K.A..(2019).Direct detection of atmospheric atomic bromine leading to mercury and ozone depletion.Proceedings of the National Academy of Sciences of the United States of America,116(29).
MLA Wang S.,et al."Direct detection of atmospheric atomic bromine leading to mercury and ozone depletion".Proceedings of the National Academy of Sciences of the United States of America 116.29(2019).
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