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    New insights into the origin of perylene in geological samples

    Access Status
    Fulltext not available
    Authors
    Grice, Kliti
    Lu, H.
    Atahan, P.
    Asif, Muhammad
    Hallman, Christian
    Greenwood, Paul
    Maslen, E.
    Tulipani, S.
    Williford, Kenneth
    Dodson, J.
    Date
    2009
    Type
    Journal Article
    
    Metadata
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    Citation
    Grice, Kliti and Lu, Hong and Atahan, Pia and Asif, M and Hallman, Christian and Greenwood, Paul and Maslen, Ercin and Tulipani, Svenja and Williford, Kenneth and Dodson, John. 2009. New insights into the origin of perylene in geological samples. Geochimica et Cosmochimica Acta. 73 (21): pp. 6531-6543.
    Source Title
    Geochimica et Cosmochimica Acta
    DOI
    10.1016/j.gca.2009.07.029
    ISSN
    00167037
    Faculty
    Department of Applied Chemistry
    School of Science and Computing
    Faculty of Science and Engineering
    Remarks

    The link to the journal’s home page is: www.elsevier.com/locate/gca

    Copyright © 2009 Elsevier B.V. All rights reserved

    URI
    http://hdl.handle.net/20.500.11937/36988
    Collection
    • Curtin Research Publications
    Abstract

    The origin of the polycyclic aromatic hydrocarbon (PAH) perylene in sediments and petroleum has been a matter of continued debate. Reported to occur in Phanerozoic organic matter (OM), fossil crinoids and tropical termite mounds, its mechanism of formation remains unclear. While a combustion source can be excluded, structural similarities to perylene quinonelike components present in e.g. fungi, plants, crinoids and insects, potentially suggest a product?precursor relationship. Here, we report perylene concentrations, 13C/12C, and D/H ratios from a Holocene sediment profile from the Qingpu trench, Yangtze Delta region, China. Perylene concentrations differ from those of pyrogenic PAHs, and rise to prominence in a stratigraphic interval that was dominated by woody vegetation as determined by palynology including fungal spores. In this zone, perylene concentrations exhibit an inverse relationship to the lignin marker guaiacol, D/H ratios between 284 o/oo and 317 o/oo, similar to the methoxy groups in lignin, as well as co-variation with spores from wood-degrading fungi. 13C/12C of perylene differs from that of land plant wax alkanes and falls in the fractionation range expected for saprophytic fungi that utilise lignin, which is isotopically lighter than cellulose and whole wood. During progressive lignin degradation, the relative carbon isotopic ratio of the perylene decreases. We therefore hypothesise a relationship of perylene to the activity of wood-degrading fungi. To support our hypothesis, we analysed a wide range of Phanerozoic sediments and oils, and found perylene to generally be present in subordinate amounts before the evolutionary rise of vascular plants, and to be generally absent from marine-sourced oils, few exceptions being attributed perhaps to a contribution of marine and/or terrestrial derived fungi, anoxia (especially under marine conditions) and/or contamination of core material by fungi. A series of low-molecular-weight aromatic quinones bearing the perylene-backbone were detected in Devonian and Cretaceous sediments, potentially representing precursor components to perylene.

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