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Elsevier, Organic Geochemistry, 2(32), p. 271-276

DOI: 10.1016/s0146-6380(00)00181-9

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Formation of mid-chain alkane keto-ols by post-depositional oxidation of mid-chain diols in Mediterranean sapropels

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

A high resolution (1 3 cm sediment intervals) organic geochemical study was carried out on the upper 50 60 cm of three box-cores (including the S1 sapropel) from eastern Mediterranean Sea sediments. The Corg, Ba/Al and Mn/Al depth profiles were used to define the oxidised and unoxidised part of the S1 sapropel. Post-depositional oxidation affected ca. 50% of the original sapropel in all three cores, resulting in a significant drop in Corg. C30 long-chain 1,15-diol and keto-ols in the extracts of these sediments were quantified by GC/MS. The vertical variation of these biomarkers in the three cores showed a common depth profile. The C30 long-chain 1,15-diol occurs almost exclusively in the unoxidised sapropel. The corresponding C30 long-chain keto-ol follows this depth profile, although the keto-ol concentrations in the unoxidised sapropel are much lower than the diol concentrations. However, the [keto-ol]/{[keto-ol]+[diol]} ratio shows a significant increase at the base of the oxidised sapropel. This suggests that the long-chain diol was transformed upon post-depositional oxidation into the chemically related long-chain keto-ol, and that this keto-ol was subsequently further oxidised. These findings indicate that long-chain keto-ols, which have no reported biological source but occur ubiquitously in marine sediments, may be formed by oxidation of long-chain diols, both in the water column and in the sediment. Author Keywords: Long-chain diols; Long-chain keto-ols; Sapropel; Mediterranean Sea; Post