論文

1997年11月

Butyltin residues in deep sea organisms collected from Surnga Bay, Japan

ENVIRONMENTAL SCIENCE & TECHNOLOGY
  • S Takahashi
  • ,
  • S Tanabe
  • ,
  • T Kubodera

31
11
開始ページ
3103
終了ページ
3109
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1021/es970032v
出版者・発行元
AMER CHEMICAL SOC

Aquatic pollution resulting from extensive usage of organotin compounds has been of great concern due to their deleterious effects in organisms. However, organotin contamination in deep-sea ecosystems has not yet been studied. The present study was attempted to determine butyltin compounds (BTs), including mono- (MBT), di- (DBT), and tributyltin (TBT) in deep-sea organisms collected from Suruga Bay, Japan, in order to elucidate the contamination status and accumulation characteristics. The organisms were collected between 135 and 980 m in the aphotic bathyal zone and compared with those collected from shallow waters. Total butyltin (Sigma BT: MBT + DBT + TBT) concentrations in the tissues of deep-sea fish, crustaceans, cephalopods, echinoderms, and gastropods were up to 980, 460, 460, 130, and 21 ng/g wet wt, respectively. These levels were lower than those in shallow-water organisms from the same bay but comparable to those reported in industrialized areas like Tokyo Bay, suggesting the expansion of BT pollution in deep-sea ecosystems. Deep-sea organisms from Suruga Bay contained much higher levels of BTs than previously reported organochlorine concentrations. BT accumulation appeared to be less lipid dependent. Among BTs, TBT was the predominant compound except in cephalopods, suggesting a fresh input of TBT into the deep-sea environment. To our knowledge, this is the first report on the detection of organotin residues in deep-sea organisms.

リンク情報
DOI
https://doi.org/10.1021/es970032v
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:A1997YE04000033&DestApp=WOS_CPL
ID情報
  • DOI : 10.1021/es970032v
  • ISSN : 0013-936X
  • Web of Science ID : WOS:A1997YE04000033

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