Use of hydrogen and carbon stable isotopes characterizing oils from the Potiguar basin (onshore), northeastern Brazil

Citation
Evd. Neto et Jm. Hayes, Use of hydrogen and carbon stable isotopes characterizing oils from the Potiguar basin (onshore), northeastern Brazil, AAPG BULL, 83(3), 1999, pp. 496-518
Citations number
84
Categorie Soggetti
Earth Sciences
Journal title
AAPG BULLETIN-AMERICAN ASSOCIATION OF PETROLEUM GEOLOGISTS
ISSN journal
01491423 → ACNP
Volume
83
Issue
3
Year of publication
1999
Pages
496 - 518
Database
ISI
SICI code
0149-1423(199903)83:3<496:UOHACS>2.0.ZU;2-0
Abstract
Hydrogen and carbon isotopic abundances were measured in representative sam ples of marine-evaporitic, lacustrine, and mixed oils from the onshore Poti guar basin. The isotopic data, together with chemical compositions and geol ogical information, were used to investigate relationships among delta D-oi l and delta 13C(oil) and source, thermal maturity: biodegradation, mixing, and the distance of secondary migration of these oils. The marine-evaporiti c 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 6 D for mixed oils are intermediate (-113 to -104 parts per thousand) between those of marine-evaporitic and lacustrine oils, showing that delta D-oil i s 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 provi de rough estimates of delta D-water in the depositional environments of the source rocks, and consequently may provide evidence about paleoclimatic co nditions at the site. Marine-evaporitic oils are enriched in C-13 (-26.5 to -25.7 parts per thous and), 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, th e mixed oils separate into two families, and a previously unrecognized comp onent possibly associated with environments that formed during the lacustri ne-to-marine transition is revealed. The investigation thus demonstrates th e superior resolving power of two-element mixing systematics.