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Impact of the Asian monsoon anticyclone on the variability of mid-to-upper tropospheric methane above the Mediterranean Basin

机译:亚洲季风抗周性通风酮对地中海盆地中上对流层甲烷变异性的影响

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The space and time variabilities of methane (CH4) total column and upper tropospheric mixing ratios are analysed above the Mediterranean Basin (MB) as part of the Chemical and Aerosol Mediterranean Experiment (ChArMEx) programme. Since the analysis of the mid-to-upper tropospheric CH4 distribution from spaceborne sensors and model outputs is challenging, we have adopted a climatological approach and have used a wide variety of data sets. We have combined spaceborne measurements from the Thermal And Near infrared Sensor for carbon Observations – Fourier Transform Spectrometer (TANSO-FTS) instrument on the Greenhouse gases Observing SATellite (GOSAT) satellite, the Atmospheric InfraRed Spectrometer (AIRS) on the AURA platform and the Infrared Atmospheric Sounder Interferometer (IASI) instrument aboard the MetOp-A platform with model results from the Chemical Transport Model (CTM) MOCAGE, and the Chemical Climate Models (CCMs) CNRM-AOCCM and LMDz-OR-INCA (according to different emission scenarios). In order to minimize systematic errors in the spaceborne measurements, we have only considered maritime pixels over the MB. The period of interest spans from 2008 to 2011 considering satellite and MOCAGE data and, regarding the CCMs, from 2001 to 2010. Although CH4 is a long-lived tracer with lifetime of ~12 years and is supposed to be well mixed in the troposphere, an east–west gradient in CH4 is observed and modelled in the mid-to-upper troposphere with a maximum in the Western MB in all seasons except in summer when CH4 accumulates above the Eastern MB. The peak-to-peak amplitude of the east–west seasonal variation in CH4 above the MB in the upper troposphere (300 hPa) is weak but almost twice as great in the satellite measurements (~25 ppbv) as in the model data (~15 ppbv). The maximum of CH4 in summer above the eastern MB can be explained by a series of dynamical processes only occurring in summer. The Asian monsoon traps and uplifts high amounts of CH4 to the upper troposphere where they build up. The Asian Monsoon Anticyclone redistributes these elevated CH4 amounts towards North Africa and the Middle East to finally reach and descend in the eastern MB. In the lower troposphere, the CH4 variability is mainly driven by the local sources of emission in the vicinity of the MB.
机译:分析了甲烷(CH4)总柱和上部对流层混合比的空间和时间变量,作为化学和气溶胶地中海实验(Charmex)计划的一部分,分析了地中海盆地(MB)。由于从星载传感器和模型输出中分析了中上部对流层CH4分布的挑战,我们采用了一种气候学方法,并使用了各种各样的数据集。我们在温室气体上占碳观测的热和近红外传感器的总空载测量 - 傅里叶变换光谱仪(TANSO-FTS)仪器观察卫星(GOSAT)卫星,Aura平台上的大气红外光谱仪(空气)和红外线大气发声器干涉仪(IASI)仪器上媒体介绍了一个平台,具有由化学传输模型(CTM)Mocage的模型,以及化学气候模型(CCMS)CNRM-AOCCM和LMDZ-OR-INCA(根据不同的发射方案) 。为了最大限度地减少在星载测量中的系统误差,我们仅考虑了MB上的海上像素。从2008年到2011年的感兴趣时期,考虑到卫星和药物数据,以及关于CCMS的,从2001年到2010年。虽然CH4是一个长期的示踪剂,寿命〜12年,应该在对流层中充分混合,在中部到上层对流层中观察到CH4中的东西梯度,在夏季夏季累积在东部MB上方的夏季,最多在西方MB中。上层上方的MB上方的EAD-WEST季节变化的峰峰值幅度(300 HPA)是弱,但在卫星测量中的两倍(〜25ppbv)如模型数据(〜 15 ppbv)。东部MB上方的夏季最大CH4可以通过夏季仅发生一系列动态过程来解释。亚洲季风捕集并将大量的CH4升高到它们积聚的上层对流层。亚洲季风抗岩旋风重新分发了这些升高的CH4朝向非洲和中东地区,最后在东部MB达到和下降。在较低的对流层中,CH4可变性主要由MB附近的局部发射源驱动。
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