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The origin of crude oils and their varied geochemical features along the western and northern slope of the Mahu depression in the Junggar Basin has been controversial. Based on the molecular and isotopic geochemistry of hydrocarbons from 46 drill-stem test crude oil samples and 36 core samples, three oil groups (I, II, III) and five subgroups (I 1 , I 2 , II, III 1 and III 2 ) have been recognized and oil-source correlations have been established. The subgroup I 1 oils originated mainly from lower Permian Fengcheng (P 1 f) carbonate source rocks, subgroup I 2 from P 1 f mudstone source rock and group II oils from Middle Permian Wuerhe (P 2 w) mudstone source rock whose potential was underestimated in the past. Group III consists of mixed oils, i.e., subgroup III 1 received contributions from P 1 f carbonates and P 2 w mudstones and subgroup III 2 is a mixture of oils from P 1 f mudstones and P 2 w-generated oils. In order to determine the main source rocks, the laboratory oil mixing experiments were carried out. Tricyclic terpane biomarker parameters (TTs) were used to quantify the source contributions. Whole oil carbon isotope ratios were also used to verify the proportions of different oils in each mixture. The results show that subgroup III 1 oils have diverse mixing ratios in different reservoir, subgroup III 2 oils are mainly from P 1 f mudstones and P 2 w source rock contributes little. Finally, the accumulation process of oil fields along the northern slope of the Mahu depression was analyzed and the contributions from different sources were revealed. This study provides an effective quantitative method to identify contributions from different lacustrine source rocks to mixed oils in the Mahu depression, which could be helpful in predicting location and composition of undiscovered oils. [ABSTRACT FROM AUTHOR]

The origin and potential source of the presalt natural gas in the Lower Paleozoic Ordovician carbonates within the Ordos Basin, China, is heavily debated, and the causes of carbon isotope reversal are currently unclear. This study analyzes the source and origin of the presalt natural gas and determines the reasons for carbon isotope reversal. The results show that the nonhydrocarbons contain CO 2 , H 2 S, and N 2 and some gas samples have high H 2 S contents of 9.02%–23.58%. The dryness coefficient (C 1 /C 1+) of 91.06%–99.99% (ave. 98.34%) suggests that the presalt gas is mainly a dry gas with some wet gas and that it originates from a high-to over-mature source. However, the results show that the presalt natural gas is primarily a wet-gas-cracking gas, rather than a kerogen-cracking gas, with a certain amount of coal-type gas mixing and it mainly originated from oil-prone marine carbonate source rocks rather than the Permian–Carboniferous coal measures. The gas has different types of carbon isotope reversal patterns, and the δ13C 2 values become negative at Ro equ > 1.5%. The mixing between the oil-cracking and wet-gas-cracking gas at Ro equ > 1.5% results in carbon isotope reversal (δ13C 1 > δ13C 2), rather than Rayleigh and migration fractionation. The occurrence of thermochemical sulfate reduction (TSR) is supported by the high abundance of H 2 S in the presalt gas, reservoir bitumen in dissolved pores, secondary calcite with negative δ13C carbonate of −21.1‰ to −9.7‰, and diagenetic cubic pyrite. It is evident that the heavy δ13C 2 values (greater than −28‰) and the carbon isotope reversal of δ13C 2 > δ13C 3 of the presalt natural gas at Ro equ < 1.5% are related to TSR. This study also establishes a new model of the carbon isotope reversal of the natural gas, which is primarily controlled by its thermal maturity and TSR. Six carbon isotope patterns can be well explained and are supported by real gas samples from the presalt strata, and two types of carbon isotope reversal are predicted. • The presalt gas is mainly oil-derived gas and dry gas with some wet gas. • Heavy δ13C 2 values (>−28‰) and carbon isotope reversal of δ13C 2 > δ13C 3 of are caused by TSR at low maturity. • The δ13C 2 values become greatly more negative at Ro equ > 1.5%. • A new model of carbon isotope reversal is established firstly, controlled by maturity and TSR. [ABSTRACT FROM AUTHOR]