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  Bromide content of sea-salt aerosol particles collected over the Indian Ocean during INDOEX 1999

Gabriel, R., von Glasow, R., Sander, R., Andreae, M. O., & Crutzen, P. J. (2002). Bromide content of sea-salt aerosol particles collected over the Indian Ocean during INDOEX 1999. Journal of Geophysical Research, 107(D19):. doi:10.1029/2001JD001133.

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資料種別: 学術論文
その他のタイトル : J. Geophys. Res.

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 作成者:
Gabriel, R.1, 著者           
von Glasow, R.2, 著者           
Sander, R.2, 著者           
Andreae, M. O.1, 著者           
Crutzen, P. J.2, 著者           
所属:
1Biogeochemistry, Max Planck Institute for Chemistry, Max Planck Society, ou_1826286              
2Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society, ou_1826285              

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キーワード: bromine; aerosol; marine boundary layer; INDOEX; leaded fuel
 要旨: [1] Bromide can be depleted from sea-salt aerosol particles in the marine boundary layer (MBL) and converted to reactive gas- phase species like Br, BrO, and HOBr, which affect ozone chemistry. Air pollution can enhance the bromine release from sea-salt aerosols and thus inject additional bromine into the MBL. During the winter monsoon the northern Indian Ocean is strongly affected by air pollution from the Indian subcontinent and Asia. As part of the Indian Ocean Experiment (INDOEX), aerosol particles were sampled with stacked filter units (SFU) on the NCAR Hercules C-130 aircraft during February-March 1999. We determined the vertical and latitudinal distribution of the major inorganic aerosol components (NH4+, Na+, K+, Mg2+, Ca2+, Cl-, NO3-, SO42-) and the Br content of the coarse aerosol to examine the role of the bromine release on the gas-phase chemistry in the marine boundary layer over the tropical Indian Ocean. The aerosol mass and composition varied significantly with air mass origin and sampling location. In the northern part of the Indian Ocean (5degrees-15degreesN, 66degrees- 73degreesE), high concentrations of pollution-derived inorganic species were found in the marine boundary layer extending from the sea surface to about 1.2 km above sea level. In this layer, the average mass concentration of all aerosol species detected by our technique was comparable to pollution levels observed in industrialized regions. In the Southern Hemisphere (1degrees- 9degreesS, 66degrees-73degreesE), the aerosol concentrations rapidly declined to remote background levels. A chloride loss from the coarse aerosol particles was observed in parallel to the latitudinal gradient of the non sea salt SO42- burden. In most of the samples, Br was depleted from the sea-salt aerosols. However, we found an enrichment in bromide in aerosols affected by air masses originating over strong pollution sources in India (Bombay, Calcutta). In these cases the additional pollution-derived Br from organo-halogen additives in petrol outweighs the release of sea-salt bromine.

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言語: eng - English
 日付: 2002-09
 出版の状態: 出版
 ページ: -
 出版情報: -
 目次: -
 査読: 査読あり
 識別子(DOI, ISBNなど): eDoc: 18180
ISI: 000180428300083
DOI: 10.1029/2001JD001133
 学位: -

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出版物 1

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出版物名: Journal of Geophysical Research
  出版物の別名 : J. Geophys. Res.
種別: 学術雑誌
 著者・編者:
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出版社, 出版地: -
ページ: - 巻号: 107 (D19) 通巻号: 8032 開始・終了ページ: - 識別子(ISBN, ISSN, DOIなど): ISSN: 0747-7309