2010
DOI: 10.1007/s11356-010-0331-1
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Brominated phenols, anisoles, and dioxins present in blue mussels from the Swedish coastline

Abstract: Clearly, all of the compounds analyzed are natural products, both in the Baltic and the North Sea. However, the geographical differences in composition may indicate different origin, e.g., due to differences in the occurrence and/or abundance of various algae species along these two coasts or possibly a more extensive dilution on the west coast.

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Cited by 54 publications
(81 citation statements)
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References 62 publications
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“…Elevated levels of those compounds were found in marine organisms (Lofstrand et al, 2010;Malmvarn et al, 2008;Marsh et al, 2004;Houde et al, 2009). Hydroxylated analogues disrupt endocrine functions more than native ones and therefore are of greater environmental concern.…”
Section: Meo/oh-substituted Pcbs/pbdesmentioning
confidence: 99%
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“…Elevated levels of those compounds were found in marine organisms (Lofstrand et al, 2010;Malmvarn et al, 2008;Marsh et al, 2004;Houde et al, 2009). Hydroxylated analogues disrupt endocrine functions more than native ones and therefore are of greater environmental concern.…”
Section: Meo/oh-substituted Pcbs/pbdesmentioning
confidence: 99%
“…High levels of hydroxylated/methoxylated PBDE derivatives in Baltic sea waters reported by several authors (Malmvarn et al, 2008;Lofstrand et al, 2010) might reflect abundance of filamentous alga along its coasts (Bonsdorff et al, 2002). Baltic wildlife could be also exposed on dioxins by way of transformation or some chlorophenols or OH-PCBs formed by way of bio-transformation of native forms (Routti et al, 2008(Routti et al, , 2009.…”
Section: Introductionmentioning
confidence: 97%
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“…in the former case being metabolites of the industrial chemicals, the PBDEs, and in the latter case originating from biosynthesis by marine organisms (Capon et al, 1981;Carté and Faulkner, 1981;Hakk and Letcher, 2003;Malmberg et al, 2005;Marsh et al, 2006). A number of naturally occurring OH-PBDEs have been structurally identified with the common feature that the hydroxy group is attached to one of the ortho-positions in the PBDE structure Teuten et al, 2005;Wan et al, 2009;Löfstrand et al, 2010;Nordlof et al, 2010). A major natural product, the 6-OH-BDE-47, is shown in Figure 17, but several other OH-PBDEs are known as natural products.…”
Section: Metabolismmentioning
confidence: 99%
“…PBDEs, MeO-PBDEs and OH-PBDEs were analyzed by gas chromatography (GC)-electron capture negative ion chemical ionization (ECNI)-mass spectrometry (MS), 5) and the PBDDs were analyzed by GC-high resolution (magnetic sector)-MS.…”
Section: Target Analysismentioning
confidence: 99%