外热带跨对流层顶混合对最下层平流层臭氧和硫酸盐气溶胶之间相关性的影响

IF 5.2 1区 地球科学 Q1 ENVIRONMENTAL SCIENCES
Philipp Joppe, Johannes Schneider, Katharina Kaiser, Horst Fischer, Peter Hoor, Daniel Kunkel, Hans-Christoph Lachnitt, Andreas Marsing, Lenard Röder, Hans Schlager, Laura Tomsche, Christiane Voigt, Andreas Zahn, Stephan Borrmann
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引用次数: 0

摘要

摘要对流层上部/平流层下部区域(UTLS)的化学成分受气团水平输送、对流系统和暖传送带内的垂直输送、快速湍流混合以及光化学生成或物种损失的影响。这导致了热带外过渡层(ExTL)的形成,该层由一氧化碳的垂直结构定义,迄今为止主要通过痕量气体相关性进行研究。在此,我们将分析范围扩大到气溶胶粒子,并通过 CAFE-EU(欧洲上空大气化学现场实验)/BLUESKY 任务期间飞机的实地测量得出欧洲中部的硫酸盐-臭氧相关性。该任务在 COVID-19 期间探测了UTLS,当时的人为排放显著减少。我们使用紧凑型飞行时间气溶胶质谱仪(C-ToF-AMS)测量了尺寸范围从约 40 纳米到 800 纳米的非难熔气溶胶粒子的化学成分。在我们的研究中,我们发现硫酸盐质量浓度与低平流层中的臭氧之间存在相关性。在测量期间,该相关性表现出一定的可变性,超过了平均硫酸盐-臭氧相关性。特别是在一次飞行中,我们观测到最下层平流层中硫酸盐气溶胶的混合比增强,痕量气体分析表明对流层对其有影响。然而,回溯轨迹表明,在过去 10 天内没有发生与对流层空气的混合。因此,我们分析了火山爆发数据库和 TROPOspheric Monitoring Instrument(TROPOMI)的卫星 SO2 回收数据,寻找可能的火山羽流和火山爆发,以解释 UTLS 中大量硫化合物的原因。通过这些分析以及前体和粒子测量的结合,我们得出结论:火山二氧化硫的气体-粒子转换导致了观测到的硫酸盐气溶胶混合比的增强。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The influence of extratropical cross-tropopause mixing on the correlation between ozone and sulfate aerosol in the lowermost stratosphere
Abstract. The chemical composition of the upper troposphere/lower stratosphere region (UTLS) is influenced by horizontal transport of air masses, vertical transport within convective systems and warm conveyor belts, rapid turbulent mixing, as well as photochemical production or loss of species. This results in the formation of the extratropical transition layer (ExTL), which is defined by the vertical structure of CO and has been studied until now mostly by means of trace gas correlations. Here, we extend the analysis to include aerosol particles and derive the sulfate–ozone correlation in central Europe from aircraft in situ measurements during the CAFE-EU (Chemistry of the Atmosphere Field Experiment over Europe)/BLUESKY mission. The mission probed the UTLS during the COVID-19 period with significantly reduced anthropogenic emissions. We operated a compact time-of-flight aerosol mass spectrometer (C-ToF-AMS) to measure the chemical composition of non-refractory aerosol particles in the size range from about 40 to 800 nm. In our study, we find a correlation between the sulfate mass concentration and O3 in the lower stratosphere. The correlation exhibits some variability exceeding the mean sulfate–ozone correlation over the measurement period. Especially during one flight, we observed enhanced mixing ratios of sulfate aerosol in the lowermost stratosphere, where the analysis of trace gases shows tropospheric influence. However, back trajectories indicate that no recent mixing with tropospheric air occurred within the last 10 d. Therefore, we analyzed volcanic eruption databases and satellite SO2 retrievals from the TROPOspheric Monitoring Instrument (TROPOMI) for possible volcanic plumes and eruptions to explain the high amounts of sulfur compounds in the UTLS. From these analyses and the combination of precursor and particle measurements, we conclude that gas-to-particle conversion of volcanic SO2 leads to the observed enhanced sulfate aerosol mixing ratios.
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来源期刊
Atmospheric Chemistry and Physics
Atmospheric Chemistry and Physics 地学-气象与大气科学
CiteScore
10.70
自引率
20.60%
发文量
702
审稿时长
6 months
期刊介绍: Atmospheric Chemistry and Physics (ACP) is a not-for-profit international scientific journal dedicated to the publication and public discussion of high-quality studies investigating the Earth''s atmosphere and the underlying chemical and physical processes. It covers the altitude range from the land and ocean surface up to the turbopause, including the troposphere, stratosphere, and mesosphere. The main subject areas comprise atmospheric modelling, field measurements, remote sensing, and laboratory studies of gases, aerosols, clouds and precipitation, isotopes, radiation, dynamics, biosphere interactions, and hydrosphere interactions. The journal scope is focused on studies with general implications for atmospheric science rather than investigations that are primarily of local or technical interest.
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