Issue 3, 2012

Stable carbon isotope composition (δ13C values) of the halogenated monoterpene MHC-1 as found in fish and seaweed from different marine regions

Abstract

Six samples of the red seaweed Plocamium cartilagineum (two both from Helgoland/Germany, Ireland, and the Antarctic) were analyzed by stable isotope analysis. The bulk δ13C values (−31 to −38‰) confirmed that this seaweed was exceptionally highly depleted in 13C. The δ15N values were in the reported range for algae, and a moderate correlation between 13C and 15N content was observed. These measurements indicated that the season had a higher impact on the δ13C values than the location. Compound specific carbon isotope analysis by gas chromatography coupled with isotope ratio mass spectrometry (GC-IRMS) was used to verify an even stronger depletion in 13C in the halogenated natural product (HNP) MHC-1 isolated from the seaweed samples. The δ13C values of MHC-1 in the range −42 to −45‰ are the lightest determined to date for polyhalogenated compounds in the molecular mass range between 250 and 800 Da. MHC-1 was also isolated from two fish samples. The much higher 13C content in MHC-1 from the fish samples (−35.6 to −39.2‰) indicated carbon isotope enrichment due to partial transformation. In processes such as the reductive debromination, the partial transformation is associated with an increase in the 13C content in the remaining non-metabolized share of a compound. Stable isotope analysis may thus provide insights into the degree of transformation of HNPs in environmental samples.

Graphical abstract: Stable carbon isotope composition (δ13C values) of the halogenated monoterpene MHC-1 as found in fish and seaweed from different marine regions

Article information

Article type
Paper
Submitted
17 Oct 2011
Accepted
05 Dec 2011
First published
17 Jan 2012

J. Environ. Monit., 2012,14, 845-851

Stable carbon isotope composition (δ13C values) of the halogenated monoterpene MHC-1 as found in fish and seaweed from different marine regions

N. Rosenfelder and W. Vetter, J. Environ. Monit., 2012, 14, 845 DOI: 10.1039/C2EM10838K

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