화학공학소재연구정보센터
AAPG Bulletin, Vol.83, No.3, 496-518, 1999
Use of hydrogen and carbon stable isotopes characterizing oils from the Potiguar basin (onshore), northeastern Brazil
Hydrogen and carbon isotopic abundances were measured in representative samples of marine-evaporitic, lacustrine, and mixed oils from the onshore Potiguar basin. The isotopic data, together with chemical compositions and geological information, were used to investigate relationships among delta D-oil and delta 13C(oil) and source, thermal maturity: biodegradation, mixing, and the distance of secondary migration of these oils. The marine-evaporitic oils are depleted in deuterium (-135 to -114 parts per thousand), and the lacustrine oils are enriched (-101 to -88 parts per thousand). Values of 6D for mixed oils are intermediate (-113 to -104 parts per thousand) between those of marine-evaporitic and lacustrine oils, showing that delta D-oil is a reliable tool to identify oils that differ genetically. Values of delta D-oil were not directly related to thermal maturation, biodegradation, or distance of the secondary migration. Hydrogen isotopic compositions of the oils can be related mainly to the delta D-water in the paleoenvironments in which the primary producers lived; therefore, delta D-oil values can provide rough estimates of delta D-water in the depositional environments of the source rocks, and consequently may provide evidence about paleoclimatic conditions at the site. Marine-evaporitic oils are enriched in C-13 (-26.5 to -25.7 parts per thousand), and lacustrine oils are depleted (-33.6 to -30.2 parts per thousand) in C-13. Relative contributions of marine-evaporitic and lacustrine sources to mixed oils thus can be calculated independently from carbon or hydrogen isotopic mixing models. When these calculations are done independently, the mixed oils separate into two families, and a previously unrecognized component possibly associated with environments that formed during the lacustrine-to-marine transition is revealed. The investigation thus demonstrates the superior resolving power of two-element mixing systematics.