Neutral and phenolic brominated organic compounds of natural and anthropogenic origin in northeast Atlantic Greenland shark (Somniosus microcephalus)
- 1 October 2010
- journal article
- research article
- Published by Wiley in Environmental Toxicology and Chemistry
- Vol. 29 (12), 2653-2659
- https://doi.org/10.1002/etc.330
Abstract
In the present study, muscle and liver tissue from 10 female Greenland sharks (Somniosus microcephalus) collected in Icelandic waters were analyzed for neutral and phenolic brominated organic compounds, including polybrominated diphenyl ethers (PBDEs) and the structurally related methoxylated (MeO) and hydroxylated (OH) PBDEs. Hydroxylated PBDEs exist both as natural products and as metabolites of the anthropogenic PBDEs, whereas MeO‐PBDEs appear to exclusively be of natural origin. Other compounds examined were 2′,6‐dimethoxy‐2,3′,4,5′‐tetrabromodiphenyl ether (2′,6‐diMeO‐BDE68), 2,2′‐dimethoxy‐3,3′,5,5′‐tetrabromobiphenyl (2,2′‐diMeO‐BB80), 2,4,6‐tribromoanisol (2,4,6‐TBA) and 2,4,6‐tribromophenol, all of natural origin, although 2,4,6‐TBA and its phenolic counterpart may also be of anthropogenic origin. The major brominated organic compound was 6‐MeO‐BDE47, and ΣMeO‐PBDE ranged from 49 to 210 ng/g fat in muscle and from 55 to 200 ng/g fat in liver tissue. Total concentrations of PBDEs were lower than ΣMeO‐PBDE, in all but one sample, ranging between 7.3 to 190 and 9.9 to 200 ng/g fat in muscle and liver, respectively, and major congeners were BDE‐47, BDE‐99, and BDE‐100. Polybrominated diphenyl ethers were analyzed using both high‐ and low‐resolution mass spectrometry (MS) as a quality assurance, and the results from this comparison were acceptable. In accordance with previous work on Greenland sharks, no size/age‐related accumulation was observed. Differences seen in concentrations were instead assumed to be a reflection of different feeding habits among the individuals. Phenolic compounds were only formed/retained in trace amounts in the Greenland shark. Among the phenolic compounds studied were 6‐OH‐BDE47, 2′‐OH‐BDE68, and 2,4,6‐tribromophenol, all detected in liver and the latter two in muscle. Environ. Toxicol. Chem. 2010;29:2653–2659. © 2010 SETACKeywords
This publication has 42 references indexed in Scilit:
- Origin of Hydroxylated Brominated Diphenyl Ethers: Natural Compounds or Man-Made Flame Retardants?Environmental Science & Technology, 2009
- In vitro hepatic metabolism of 2,2′,4,4′,5-pentabromodiphenyl ether (BDE 99) in Chinook Salmon (Onchorhynchus tshawytscha)Aquatic Toxicology, 2009
- Organochlorines and polybrominated diphenyl ethers in four geographically separated populations of Atlantic salmon (Salmo salar)Journal of Environmental Monitoring, 2007
- Distribution, reproduction and feeding of the Greenland shark Somniosus (Somniosus) microcephalus, with notes on two other sleeper sharks, Somniosus (Somniosus) pacificus and Somniosus (Somniosus) antarcticusJournal of Fish Biology, 2007
- Identification and Quantification of Polybrominated Hexahydroxanthene Derivatives and Other Halogenated Natural Products in Commercial Fish and Other Marine SamplesJournal of Agricultural and Food Chemistry, 2006
- Two Abundant Bioaccumulated Halogenated Compounds Are Natural ProductsScience, 2005
- Polybrominated diphenyl ethers (PBDEs) and their methoxylated derivatives in pike from Swedish waters with emphasis on temporal trends, 1967–2000Environmental Pollution, 2004
- Synthesis of Hydroxylated and Methoxylated Polybrominated Diphenyl Ethers − Natural Products and Potential Polybrominated Diphenyl Ether MetabolitesEuropean Journal of Organic Chemistry, 2003
- Bromochloromethoxybenzenes in the Marine Troposphere of the Atlantic Ocean: A Group of Organohalogens with Mixed Biogenic and Anthropogenic OriginEnvironmental Science & Technology, 1998
- Synthesis and Characterization of Polybrominated Diphenyl Ethers -- Unlabelled and Radiolabelled Tetra-, Penta- and Hexabromodiphenyl Ethers.Acta Chemica Scandinavica, 1996