CHEMISTRY OF ANTARCTIC ATMOSPHERIC AEROSOLS
Inland atmospheric aerosols were sampled by members of JARE-29 (1988-1989) using a modified Andersen type cascade impacter, which consists of 12 impacter stages and a back-up filter and can fractionate aerosol particles down to 0.04 micron. MSA (methane sulfonic acid) and nssSO_4 showed their maximu...
Main Authors: | , , , , , , , , , |
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Format: | Report |
Language: | English |
Published: |
ABSTRACT
1992
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Subjects: | |
Online Access: | https://nipr.repo.nii.ac.jp/?action=repository_uri&item_id=3755 http://id.nii.ac.jp/1291/00003755/ https://nipr.repo.nii.ac.jp/?action=repository_action_common_download&item_id=3755&item_no=1&attribute_id=18&file_no=1 |
Summary: | Inland atmospheric aerosols were sampled by members of JARE-29 (1988-1989) using a modified Andersen type cascade impacter, which consists of 12 impacter stages and a back-up filter and can fractionate aerosol particles down to 0.04 micron. MSA (methane sulfonic acid) and nssSO_4 showed their maximum in size distribution at 0.2-0.3 micron. Their distribution curves run parallel with similar trend and strongly suggest their same or closely related origin. Na has its maximum at 0.6-0.7 micron; its marine origin is indicated by the similar trend of Mg and also by the Mg/Na ratio close to that in seawater. Therefore, MSA and nssSO_4 ratio at the peak of size distribution was at nearly 0.1,which is higher than 0.2 over the Antarctic sea and at Syowa Station, and suggests their supply from a warmer low-latitude sea area. |
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