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Contributed Articles

Forensic Fingerprinting of Biomarkers for Oil Spill Characterization and Source Identification

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Pages 105-146 | Received 08 Aug 2005, Accepted 25 Jan 2006, Published online: 23 Feb 2007
 

Biomarkers are one of the most important hydrocarbon groups in petroleum. Biomarkers can be detected in low quantities (ppm and sub-ppm level) in the presence of a wide variety of other types of petroleum hydrocarbons by the use of the gas chromatography/mass spectrometry (GC/MS). Relative to other hydrocarbon groups in oil such as alkanes and most aromatic compounds, biomarkers are more degradation-resistant in the environment. Furthermore, biomarkers formed under different geological conditions and ages may exhibit different biomarker fingerprints. Therefore, chemical analysis of biomarkers generates information of great importance to environmental forensic investigations in terms of determining the source of spilled oil, differentiating and correlating oils, and monitoring the degradation process and weathering state of oils under a wide variety of conditions. This article briefly reviews biomarker chemistry, biomarker characterization and quantification, biomarker distributions, weathering effects on biomarker composition, bicyclic biomarker sesquiterpanes and diamondoids, diagnostic ratios and cross-plots of biomarkers, unique biomarkers, application of biomarker fingerprinting techniques for spill source identification, and application of multivariate statistical analysis for biomarker fingerprinting.

Notes

*The diagnostic ratios in Table 6 consist of alkanes, terpanes, steranes, sesquiterpanes, and diamondoids. Ratios are defined from Eq. (1) for simplicity, but can be readily redefined using Eqs. (2) and (3). For example, in accordance with Eq. (2), the ratio of C29α β -30-norhopane/C30α β hopane (H29/H30) can be readily redefined as H29/(H29 + H30).

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