通过使用TROPOMI的观测约束区域模型揭示2020年欧洲封锁引起的臭氧升高的途径。

IF 5.2 1区 地球科学 Q1 ENVIRONMENTAL SCIENCES
Amir H Souri, Kelly Chance, Juseon Bak, Caroline R Nowlan, Gonzalo González Abad, Yeonjin Jung, David C Wong, Jingqiu Mao, Xiong Liu
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引用次数: 16

摘要

关于在COVID-19封锁期间排放如何变化的问题无法仅通过观测大气微量气体浓度来回答,部分原因是大气输送、排放、动力学、光化学和化学反馈同时发生变化。利用特征良好的观测资料,利用多物种反演框架进行的化学输运模式模拟应能区分这些影响,从而能够仔细检查排放的变化。因此,我们在2020年3月、4月和5月(封锁)和2019年(基线)期间,使用表征良好的对流层监测仪器(TROPOMI) HCHO和NO2柱,共同限制nox和VOC的排放。我们观察到,2020年3月,包括巴黎、伦敦、马德里和米兰在内的几个主要城市的氮氧化物排放量明显下降(14% - 31%),4月进一步扩大到罗马、布鲁塞尔、法兰克福、华沙、贝尔格莱德、基辅和莫斯科(34% - 51%)。然而,与基线相比,2020年3月,英国、波兰和莫斯科的部分地区的nox排放量保持在一些相似的值,甚至更高,这可能是由于限制的时间表。与地面监测站的比较表明,约束模型未充分反映地表NO2的减少情况。这种代表性不足与受云层影响的TROPOMI频率有关。在4月份,当有充足的TROPOMI样品存在时,模型很好地描述了污染地区表面NO2的减少(模型:-21±17%,观测:-29±21%)。除低纬度地区外,对挥发性有机化合物排放的观测约束一般较弱。结果支持在封锁期间地表臭氧增加。4月份,约束模式与地表观测到的最大日8 h平均值(MDA8)臭氧变化(r = 0.43)基本一致,特别是在臭氧增强普遍存在的中欧地区(模式:+3.73±3.94%,+ 1.79 ppbv,观测:+7.35±11.27%,+3.76 ppbv)。该模式表明,干沉降、平流和扩散等物理过程使MDA8同月平均臭氧减少-4.83 ppbv,而被大量负的jno2 [no2] - kno3 + o3 [NO] [o3]抑制的臭氧产出率减少,导致臭氧增加+5.89 ppbv。涉及固定人为排放的实验表明,气象学对同一地区MDA8表面臭氧增加的贡献为42%,其余部分(58%)来自人为排放的变化。结果表明,主要臭氧前体的卫星数据能够帮助大气模式捕捉由突变发射异常引起的臭氧变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Unraveling pathways of elevated ozone induced by the 2020 lockdown in Europe by an observationally constrained regional model using TROPOMI.

Unraveling pathways of elevated ozone induced by the 2020 lockdown in Europe by an observationally constrained regional model using TROPOMI.

Unraveling pathways of elevated ozone induced by the 2020 lockdown in Europe by an observationally constrained regional model using TROPOMI.

Unraveling pathways of elevated ozone induced by the 2020 lockdown in Europe by an observationally constrained regional model using TROPOMI.

Questions about how emissions are changing during the COVID-19 lockdown periods cannot be answered by observations of atmospheric trace gas concentrations alone, in part due to simultaneous changes in atmospheric transport, emissions, dynamics, photochemistry, and chemical feedback. A chemical transport model simulation benefiting from a multi-species inversion framework using well-characterized observations should differentiate those influences enabling to closely examine changes in emissions. Accordingly, we jointly constrain NO x and VOC emissions using well-characterized TROPOspheric Monitoring Instrument (TROPOMI) HCHO and NO2 columns during the months of March, April, and May 2020 (lockdown) and 2019 (baseline). We observe a noticeable decline in the magnitude of NO x emissions in March 2020 (14 %-31 %) in several major cities including Paris, London, Madrid, and Milan, expanding further to Rome, Brussels, Frankfurt, Warsaw, Belgrade, Kyiv, and Moscow (34 %-51 %) in April. However, NO x emissions remain at somewhat similar values or even higher in some portions of the UK, Poland, and Moscow in March 2020 compared to the baseline, possibly due to the timeline of restrictions. Comparisons against surface monitoring stations indicate that the constrained model underrepresents the reduction in surface NO2. This underrepresentation correlates with the TROPOMI frequency impacted by cloudiness. During the month of April, when ample TROPOMI samples are present, the surface NO2 reductions occurring in polluted areas are described fairly well by the model (model: -21 ± 17 %, observation: -29 ± 21 %). The observational constraint on VOC emissions is found to be generally weak except for lower latitudes. Results support an increase in surface ozone during the lockdown. In April, the constrained model features a reasonable agreement with maximum daily 8 h average (MDA8) ozone changes observed at the surface (r = 0.43), specifically over central Europe where ozone enhancements prevail (model: +3.73 ± 3.94 %, + 1.79 ppbv, observation: +7.35 ± 11.27 %, +3.76 ppbv). The model suggests that physical processes (dry deposition, advection, and diffusion) decrease MDA8 surface ozone in the same month on average by -4.83 ppbv, while ozone production rates dampened by largely negative J NO 2 [ NO 2 ] - k NO + O 3 [ NO ] [ O 3 ] become less negative, leading ozone to increase by +5.89 ppbv. Experiments involving fixed anthropogenic emissions suggest that meteorology contributes to 42 % enhancement in MDA8 surface ozone over the same region with the remaining part (58 %) coming from changes in anthropogenic emissions. Results illustrate the capability of satellite data of major ozone precursors to help atmospheric models capture ozone changes induced by abrupt emission anomalies.

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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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