New insights into the origin of perylene in geological samples

被引:189
作者
Grice, Kliti [1 ]
Lu, Hong [1 ,2 ]
Atahan, Pia [1 ,3 ,4 ]
Asif, Muhammad [1 ]
Hallmann, Christian [1 ]
Greenwood, Paul [1 ,5 ,6 ]
Maslen, Ercin [1 ]
Tulipani, Svenja [1 ]
Williford, Kenneth [1 ]
Dodson, John [4 ]
机构
[1] Curtin Univ Technol, WA Organ & Isotope Geochem Ctr, Inst Geosci Res, Dept Appl Chem, Perth, WA 6845, Australia
[2] Chinese Acad Sci, Guangzhou Inst Geochem, Guangzhou, Guangdong, Peoples R China
[3] Univ Western Australia, Sch Earth & Geog Sci, Perth, WA 6009, Australia
[4] Australian Nucl Sci & Technol Org, Inst Environm Res, Menai, NSW 2234, Australia
[5] Univ Western Australia, John De Laeter Mass Spectrometry Ctr M090, Crawley, WA 6009, Australia
[6] Univ Western Australia, WA Biogeochem Ctr M090, Crawley, WA 6009, Australia
关键词
POLYCYCLIC AROMATIC-HYDROCARBONS; YANGTZE-RIVER DELTA; ENVIRONMENTAL-CHANGE; PERTH BASIN; SEDIMENTS; PIGMENTS; ISOTOPE; POLLEN; COMPONENTS; BIOMARKER;
D O I
10.1016/j.gca.2009.07.029
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
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 quinone-like components present in e. g. fungi, plants, crinoids and insects, potentially suggest a product-precursor relationship. Here, we report perylene concentrations, C-13/C-12, and D/H ratios from a Holocene sediment pro. le 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 parts per thousand and -317 parts per thousand, similar to the methoxy groups in lignin, as well as co-variation with spores from wood-degrading fungi. C-13/C-12 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. Crown copyright (C) 2009 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:6531 / 6543
页数:13
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