Japan Geoscience Union Meeting 2014

Presentation information

Oral

Symbol A (Atmospheric, Ocean, and Environmental Sciences) » A-AS Atmospheric Sciences, Meteorology & Atmospheric Environment

[A-AS22_1AM2] Atmospheric Chemistry

Thu. May 1, 2014 11:00 AM - 12:45 PM 511 (5F)

Convener:*Nobuyuki Takegawa(Research Center for Advanced Science and Technology, University of Tokyo), Yousuke Sawa(Geochemical Research Department, Meteorological Research Institute), Yugo Kanaya(Research Institute for Global Change, Japan Agency for Marine-Earth Science and Technology), Kenshi Takahashi(Research Institute for Sustainable Humanosphere, Kyoto University), Hiroshi Tanimoto(National Institute for Environmental Studies), Chair:Kazuhiro Tsuboi(Oceanography and Geochemistry Research Department,Meteorological Research Institute)

11:30 AM - 11:45 AM

[AAS22-17] Methyl chloride in the upper troposphere observed by CARIBIC: large-scale distributions and Asian summer monsoon outflow

*Taku UMEZAWA1, Angela K. BAKER1, David ORAM2, Carina SAUVAGE1, Debbie O'SULLIVAN2, Armin RAUTHE-SCHOECH1, Stephen A. MONTZKA3, Andreas ZAHN4, Carl A.M. BRENNINKMEIJER1 (1.Max Planck Institute for Chemistry, 2.National Centre for Atmospheric Science, School of Environmental Sciences, University of East Anglia, 3.Earth System Research Laboratory, NOAA, 4.Institute for Meteorology and Climate Research, Karlsruhe Institute of Technology)

Keywords:CARIBIC, aircraft observation, methyl chloride, upper troposphere

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.