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With the continuous increase in exploration efforts in new zones and new strata, significant breakthroughs have been made in the natural gas exploration of the O¹m56 to O1m4 formations in the Ordos Basin. Thus, the origin and exploration potential of subsalt natural gas have attracted much attention and urgently need to be addressed. On the basis of certain geochemical characteristics, genetic types, and sources of natural gas, a comprehensive study on the sedimentary environment, organic geochemical characteristics, and spatial distribution scale of source rocks are conducted in this paper by using geological and geochemical methods. The study shows that: (1) The Ordovician subsalt natural gas is mainly "pyrolysis dry gas," among which the δ13C1 of Ordovician subsalt low sulfur (sulfur-free) natural gas is lighter, with an average value of -39.6‰; the δ13C2 ranges more largely from -35.6‰ to -25.8‰. In contrast, both δ13C1 and δ13C2 values are heavier in high-sulfur natural gas, revealing that different Thermochemical Sulfate Reduction (TSR) reaction stages have different degrees of influence on natural gas components and carbon isotope composition. (2) Subsalt natural gas is classified as "oil-type gas," which is self-generated and self-accumulated, whose source rocks are mainly Ordovician subsalt marine deposits. (3) Three types of marine source rocks are developed in Ordovician subsalt, including black argillaceous rock, dark argillaceous dolomite (dolomitic mudstone), and dark micrite (bioclastic) limestone. In addition to micrite limestone, these rocks were mainly formed in a confined lagoon sedimentary environment with high salinity and anoxia. Sedimentary water was significantly stratified and the environment was highly reduced. The organic matter content of the source rocks is relatively high, with an average TOC value of 0.45%. The hydrocarbon-generating parent materials are mainly composed of bacteria and algae, and the organic matter evolution reaches highover maturity stage. The total gas generation amount of the marine source rocks in Ordovician subsalt is approximately 43.8 × 1012 m³, which can provide hydrocarbons and accumulate for the subsalt favorable reservoir facies located far from Upper Paleozoic gas sources. [ABSTRACT FROM AUTHOR]

Water, in ultra-deep layers of the earth and in layers receiving abnormally high heat, can exist in a supercritical state. Supercritical water (SCW) can participate in the transformations of organic compounds not only as a solvent but also as a reactant, influencing petroleum formation and the evolution of sedimentary organic matter. Here, we carried out hydrous pyrolysis experiments in both SCW and water vapor (WV) using two organic-rich marine rocks under closed conditions, to quantitatively evaluate the generation potential of hydrocarbons in a supercritical state and to clarify the effect of water phase on hydrous pyrolysis experiments. The results showed that SCW promoted gaseous and liquid hydrocarbon generation and facilitated the cracking of aliphatic hydrocarbons. For gaseous hydrocarbons, the action of SCW became stronger as the temperature increased. For liquid hydrocarbons, the peak yields of bitumen were enhanced by the SCW, and the temperature corresponding to peak yield in SCW was lower than that in WV. These results were attributed to the supply of hydrogen and oxygen from SCW for the petroleum formation and cracking. The δ13C and δD values of gases were also influenced by SCW. However, these values obtained in SCW did not always become positive as their yields increased. Generally, methane (CH4) was enriched in 12C and ¹H. The influence of SCW on the isotopic fractionation of ethane (C2H6) and propane (C3H8) was more complex. The water phase is an important factor affecting the experimental results of hydrous pyrolysis. From these findings, it can be concluded that SCW allowed for increased conversion of sedimentary organic matter to gaseous and liquid hydrocarbons in ultra-deep layers and layers affected by volcanic-hydrothermal activity. [ABSTRACT FROM AUTHOR]