Persisting volcanic ash particles impact stratospheric SO2 lifetime and aerosol optical properties

被引:65
|
作者
Zhu, Yunqian [1 ]
Toon, Owen B. [1 ,2 ]
Jensen, Eric J. [3 ]
Bardeen, Charles G. [3 ]
Mills, Michael J. [3 ]
Tolbert, Margaret A. [4 ]
Yu, Pengfei [5 ,7 ]
Woods, Sarah [6 ]
机构
[1] Univ Colorado, Lab Atmospher & Space Phys, Boulder, CO 80303 USA
[2] Univ Colorado, Dept Atmospher & Ocean Sci, Boulder, CO 80302 USA
[3] Natl Ctr Atmospher Res, Atmospher Chem Observat & Modeling Lab, Boulder, CO 80301 USA
[4] Univ Colorado, Cooperat Inst Res Environm Sci, Boulder, CO 80309 USA
[5] NOAA, Earth Syst Res Lab, Boulder, CO 80305 USA
[6] Stratton Pk Engn Co Inc, Boulder, CO 80301 USA
[7] Jinan Univ, Inst Environm & Climate Res, Guangzhou, Peoples R China
基金
美国国家科学基金会;
关键词
SULFUR-DIOXIDE; MICROPHYSICAL SIMULATIONS; AIRCRAFT OBSERVATIONS; JUNE; 1991; FINE ASH; PINATUBO; OXIDATION; ERUPTIONS; ADSORPTION; EMISSIONS;
D O I
10.1038/s41467-020-18352-5
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Volcanic ash is often neglected in climate simulations because ash particles are assumed to have a short atmospheric lifetime, and to not participate in sulfur chemistry. After the Mt. Kelut eruption in 2014, stratospheric ash-rich aerosols were observed for months. Here we show that the persistence of super-micron ash is consistent with a density near 0.5 g cm(-3), close to pumice. Ash-rich particles dominate the volcanic cloud optical properties for the first 60 days. We also find that the initial SO2 lifetime is determined by SO2 uptake on ash, rather than by reaction with OH as commonly assumed. About 43% more volcanic sulfur is removed from the stratosphere in 2 months with the SO2 heterogeneous chemistry on ash particles than without. This research suggests the need for re-evaluation of factors controlling SO2 lifetime in climate model simulations, and of the impact of volcanic ash on stratospheric chemistry and radiation.
引用
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页数:11
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