Abstract
The Lower Jurassic Ziliujing Formation in China’s Sichuan Basin is a significant shale target for exploration; however, the strong heterogeneity of the properties of organic matter (OM) in shale makes it challenging to identify the target area for exploration, and the mechanism of OM enrichment is still unclear. Furthermore, the mechanisms of the response of the Da’anzhai member to the Toarcian Oceanic Anoxic Event (T-OAE) are controversial. Previous studies have focused on sedimentary facies analysis based on mineralogy and elemental abundances and have provided minimal information about organic geochemistry, which adds to the challenge of deeply understanding the influence of the T-OAE on the molecular geochemical characteristics of the Da’anzhai member. In this study, the Da’anzhai member of the Lower Jurassic Ziliujing Formation in the Langzhong area, Sichuan Basin, is studied via X-ray diffraction, total organic carbon, gas chromatography–mass spectrometry, organic carbon isotope, organic petrographical and pyrolysis analyses. To accurately identify the trend of the paleosedimentary environmental proxies, the Mann‒Kendall test is utilized to identify the trend of the data. Our results show that the Da’anzhai shale was deposited in a dysoxic transitional environment to an intermittent reducing environment with freshwater to brackish conditions. The response to the T-OAE can be identified in the middle and upper parts of the middle submember and the bottom of the upper submember of the Da’anzhai member. The T-OAE influenced the redox conditions, salinity, and OM origins during deposition in the middle of the Da’anzhai member, which resulted in the enrichment of OM. The abnormally high C30 diahopane/C30 hopane (C30D/C30H) ratio can be considered a potential proxy for locating the section of strata that responded to the T-OAE in the Da’anzhai member. In the study area, the mechanism of the response of the Da’anzhai shale to the T-OAE manifested as an improvement in hydrological cycling rather than a marine incursion. Our study provides new information that deepens the understanding of the mechanisms of the response of lacustrine shales to oceanic anoxic events from the perspective of molecular organic geochemistry.
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