Neon as a Criterion for Noble Gas Distribution between Gas Accumulations and Edgewater
摘要
The relationships of Ne isotopic composition with Ne and N2 partial pressures and N2/Ne ratio in gas accumulations was analyzed for the first time. The influence of groundwater on the contents and isotopic compositions of noble gases in CO2, N2, and CH4 gas reservoirs was also evaluated. It was shown that Ne partial pressure in different gas accumulations increases in the sequence CO2–CH4–N2. Neon with the mantle isotope signature is typical of CO2 accumulations, whereas N2 accumulations are dominated by a mixture of atmospheric and crustal Ne (20Ne/22Ne is 8.9–10.2, and 21Ne/22Ne is 0.040–0.083). The initial concentration and isotopic composition of Ne and certainly other noble gases depend on the formation conditions of the gas phase that enters the reservoir. Subsequently, Ne partial pressure increases in the CO2 and CH4 gas accumulations but decreases in the N2 gas accumulations, supposedly owing to gas exchange with groundwater. We proposed a model for gas exchange between a gas reservoir and groundwater, which allowed us to estimate the distribution of noble gases between them. (1) CO2 entering reservoirs has a negligible partial pressure of mantle Ne (∼0.008 Pa). Therefore, the fraction of Ne from groundwater in them may be as high as 90%. (2) In contrast, N2 reservoirs have the atmospheric Ne isotopic signature with an admixture of a nucleogenic (crustal) component and Ne partial pressure higher than in the atmosphere. The N2 gas phase was most likely derived from ancient Ca–Cl brines under a formation pressure of less than 300 bar. (3) The isotopic composition of Ne from CH4 reservoirs is consistent with the assumption that microbial CH4 is formed under near-surface conditions (atmospheric gases dominate), and thermogenic CH4 is formed at greater depths. Neon and N2 in thermogenic CH4 was probably produced by gas exchange with Ca–Cl brines. In general, the isotopic composition of Ne in CH4 reservoirs reflects the mixing of microbial and thermogenic CH4 during migration to the surface.