Japan Geoscience Union Meeting 2014

Presentation information

Oral

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

[A-AS22_1AM1] Atmospheric Chemistry

Thu. May 1, 2014 9:00 AM - 10:45 AM 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:Takuma Miyakawa(Japan Agency for Marine-Earth Science and Technology)

10:15 AM - 10:30 AM

[AAS22-13] Mixing states of summer time aerosol particles in Noto peninsula

*Reina YAMADA1, Yusuke KAMIGUCHI1, Kento KINOUCHI2, Yoko IWAMOTO3, Sayako UEDA4, Kouji ADACHI5, Atsushi MATSUKI3 (1.College of Science and Engineering, Kanazawa University, 2.Graduate School of Natural Science and Technology, Kanazawa University, 3.Institute of Nature and Environmental Technology, Kanazawa University, 4.Solar-Terrestrial Environment Laboratory, Nagoya University, 5.Meteorological Research Institute)

Keywords:atmospheric aerosols, mixing state, organic aerosol particles, sulfate aerosol particles

Mixing state is one of the factors that determine the characteristic of aerosol particles, and it is important for evaluating their climatic impact. Until recently, summer time aerosol particles in the remote region of central Japan didn’t attract much attention since human influence was considered minimal during the season. However, our measurement in the last few years showed that particle number concentrations in summer time were the highest in all seasons. In order to understand the characteristics of the summer time aerosols, we analyzed composition and mixing state of individual particles using transmission electron microscopy (TEM) coupled to energy dispersive W-ray spectrometer (EDX). We conducted quasi-daily sampling at research facility NOTOGRO (NOTO Ground-based Research Observatory) situated at tip of the Noto peninsula from 9th, Jun to 23rd, August. Samples collected during episodes of high aerosol loadings were selected and analyzed. Winds tend to transport air-mass from the Pacific Ocean to the sampling site in summer. However, we found that there were some other flow patterns including flow from the continent of Asia, associated with the high aerosol concentrations. Major composition of particles differed depending on the flow patterns. In addition, many particles were internally mixed, and organics were predominant in smaller diameter range, while sulfates were predominant in larger diameter range. Above results showed that, depending e.g. on the difference of the flow patterns, mixing state of aerosols observed in high concentrations in summer exhibit high temporal variability, and such mixing state are often unevenly distributed among different particle sizes.