4.6 Article

Influence of thermochemical sulfate reduction on oxygen isotopic composition of calcite cements in carbonates of the Triassic Feixianguan and Permian Changxing formations in the Sichuan Basin, China

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FRONTIERS IN EARTH SCIENCE
卷 10, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/feart.2022.1030472

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calcite cement; diagenesis; oxygen-isotopic composition; thermochemical sulfate reduction; Sichuan Basin

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This study analyzed the stable isotope compositions of calcite cements in carbonate formations from four carbonate fields in the Sichuan Basin. The results showed that some calcite cements had similar δ18O values to their host carbonates, despite forming at high temperatures (>100 degrees C). Petrographic and geochemical analysis indicated that the δ18O-enriched calcites were commonly associated with solid bitumens and had lower δ13C values, suggesting the involvement of thermochemical sulfate reduction. Based on the findings, a model for oxygen isotope behavior during thermochemical sulfate reduction was established.
Calcite cement is a common diagenetic mineral in carbonate rocks and plays an important role on rock quality as hydrocarbon reservoirs. Traditionally, oxygen isotopic compositions (delta O-18) of the diagenetic calcites tend to decrease with increasing depths due to temperature-dependent isotope fractionation. In this study, the stable isotope compositions of the calcite cements in the Changxing and Feixianguan formations from the Puguang, Yuanba, Jiannan and Fuling carbonate fields in the Sichuan Basin were analyzed. The results show that some calcite cements have delta O-18 values similar to those of their host carbonates, despite the fact that these calcites formed at elevated temperatures(>similar to 100 degrees C). Based on petrographic and geochemical analyses, the O-18-enriched calcites commonly occur with solid bitumens and have lower delta C-13 values compared with host rocks, suggesting thermochemical sulfate reduction (TSR) provided organic carbon for these calcite precipitation. During TSR, thermal oxidation of hydrocarbons generated the light carbon, and simultaneously the reduced sulfate ions provided the oxygen. Comparison of our study with the TSR calcites worldwide, a model for oxygen isotope behavior during TSR was established. Oxygen isotope compositions of TSR-related calcites are a function of isotope compositions and amounts of the initial anhydrite and pore waters. TSR shows two opposing effects on the delta O-18 values of calcites, depending on the delta O-18 ratios of the initial anhydrite. The reduction of anhydrite with relatively low delta O-18 values causes the calcite delta O-18 lower than theoretical values of calcites directly precipitated from pore waters. The heavy delta O-18 ratios of calcites formed during TSR are not only attributed to the O-18-enriched pore water resulting from extensive water-rock interaction, but also probably due to the involvement of anhydrite with high delta O-18 values.

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