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Synchronous negative carbon isotope shifts in marine and terrestrial biomarkers at the onset of the early Aptian oceanic anoxic event 1a: Evidence for the release of <sup>13</sup>C‐depleted carbon into the atmosphere
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Citations
66
References
2007
Year
Organic GeochemistryBiogeochemistryMarine GeologyOrganic MaterialEngineeringPaleoceanographyPrecambrian GeologyIsotope GeochemistryOrganic MatterEarly DiagenesisTerrestrial Organic MatterMarine ChemistryTerrestrial BiomarkersStable Isotope ProbingGeochemistryOceanographyCarbon CycleEarth Science
A common feature of records of the early Aptian oceanic anoxic event (OAE) 1a is the sharp negative δ 13 C excursion displayed in both carbonate and organic matter at the onset of this event. A synchronous negative δ 13 C excursion has also been noted for terrestrial organic matter. This negative excursion has been attributed to either an injection of 13 C‐depleted light carbon into the atmosphere or, in case of marine sediments, recycling of 13 C‐depleted CO 2 . However, most studies were done on separate cores, and no information on the relative timing of the negative spikes in terrestrial versus marine records has been obtained. Here we examine early Aptian core sections from two geographically distal sites (Italy and the mid‐Pacific) to elucidate the causes and relative timing of this negative “spike.” At both sites, increased organic carbon (C org ) and decreased bulk carbonate contents characterize the interval recording OAE 1a (variously referred to as the “Selli event”). The organic material within the “Selli level” is immature and of autochthonous origin. Measured δ 13 C values of marine and terrestrial biomarkers largely covary with those of bulk organic carbon, with lowest values recorded at the base of the organic‐rich section. By contrast, sediments enveloping the “Selli level” exhibit very low C org contents, and their extractable C org is predominantly of allochthonous origin. Hydrous pyrolysis techniques used to obtain an autochthonous, pre‐Selli δ 13 C value for algal‐derived pristane from corresponding sample material yielded a negative δ 13 C shift of up to 4‰. A negative δ 13 C shift of similar magnitude was also measured for the terrigenous n ‐alkanes. The results are collectively best explained by means of a massive, syndepositional, rapid input of 13 C‐depleted carbon into the atmosphere and surface oceans, likely delivered either via methane produced from the dissociation of sedimentary clathrates or perhaps by widespread thermal metamorphism of C org ‐rich sedimentary rocks.
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