日本地球惑星科学連合2014年大会

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セッション記号 A (大気海洋・環境科学) » A-AS 大気科学・気象学・大気環境

[A-AS22_1AM2] 大気化学

2014年5月1日(木) 11:00 〜 12:45 511 (5F)

コンビーナ:*竹川 暢之(東京大学先端科学技術研究センター)、澤 庸介(気象研究所地球化学研究部)、金谷 有剛(独立行政法人海洋研究開発機構地球環境変動領域)、高橋 けんし(京都大学生存圏研究所)、谷本 浩志(国立環境研究所)、座長:坪井 一寛(気象研究所 海洋・地球化学研究部)

11:30 〜 11:45

[AAS22-17] CARIBICで観測された上部対流圏の塩化メチル変動:広域分布と夏季のアジアモンスーンからの流出

*梅澤 拓1K. Baker Angela1Oram David2Sauvage Carina1O'Sullivan Debbie2Rauthe-Schoech Armin1A. Montzka Stephen3Zahn Andreas4A.M. Brenninkmeijer Carl1 (1.ドイツマックスプランク化学研究所、2.英国イーストアングリア大学、3.米国海洋大気庁地球システム調査研究所、4.ドイツカールスルーエ工科大学)

キーワード:CARIBIC, 航空機観測, 塩化メチル, 上部対流圏

CARIBIC is a flying observatory onboard a Lufthansa A340-600 aircraft that observes various atmospheric compounds at almost monthly intervals. In this study, we present spatial and temporal variations of methyl chloride (CH3Cl) in the upper troposphere (UT) observed mainly by CARIBIC for the years 2005-2011. The CH3Cl mixing ratio in the UT over Europe was higher than that observed at a European surface baseline station throughout the year, indicative of a persistent positive vertical gradient at NH mid latitudes. A series of flights over Africa and South Asia show that CH3Cl mixing ratios increase toward tropical latitudes, and the observed UT CH3Cl level over these two regions and the Atlantic was higher than that measured at remote surface sites. Strong emissions of CH3Cl in the tropics combined with meridional air transport through the UT may explain such vertical and latitudinal gradients. Comparisons with carbon monoxide (CO) data indicate that non-combustion sources in the tropics dominantly contribute to forming the latitudinal gradient of CH3Cl in the UT. We also observed elevated mixing ratios of CH3Cl and CO in air influenced by biomass burning in South America and Africa, and the emission ratios derived for CH3Cl to CO in those regions agree with previous observations. In contrast, correlations indicate a high CH3Cl to CO ratio of 2.9±0.5 ppt ppb-1 in the Asian summer monsoon anticyclone and domestic biofuel emissions in South Asia are inferred to be responsible. We estimated the CH3Cl emission in South Asia to be 134±23 Gg Cl yr-1, which is higher than a previous estimate due to the higher CH3Cl to CO ratio observed in this study.