Elsevier

Chemical Geology

Volume 74, Issues 1–2, 30 December 1988, Pages 67-97
Chemical Geology

A petrographic and geochemical model for the origin of calcite cap rock at Damon Mound salt dome, Texas, U.S.A.

https://doi.org/10.1016/0009-2541(88)90147-7Get rights and content

Abstract

Calcite cap rock at Damon Mound, Texas, consists of five calcite generations recognizable through standard petrography and cathodoluminescence. Stage-IA calcite formed by dissolution of anhydrite followed by calcite precipitation and was partly replaced by stage-IB calcite. Stage II formed above stage-IA and -IB substrates either filling open voids or cementing breccia fragments. Stage-IIIA and -IIIB calcites fill late fractures that crosscut all previously formed generations.

Microprobe analysis indicates that each calcite generation is geochemically distinct. Sr/Mg ratios indicate that calcite precipitated from variable proportions of formation water, meteoric water, and/or seawater.

Wide variation in calcite fluid-inclusion compositions (1.0–9.4 eq.wt.% NaCl) indicates mixing of high-salinity water and low-salinity meteoric water. The single-phase nature of most fluid inclusions and the homogenization temperatures indicate that calcite precipitated at temperatures of <70°C.

Calcite δ13C-values range from −31.1 to −14.4‰ (PDB), generally decrease with depth, and are most similar to crude-oil δ13C-values. Calcite δ18O-values range from −7.6 to −4.8‰ (PDB), generally increase with depth, and are compatible with derivation from local meteoric water or formation water at high temperature. Late-stage calcite can be either isotopically heavier or lighter than adjacent early-stage calcite with regard to both carbon and oxygen, and because isotopic values vary with depth, it appears that fluid mixing is the mechanism most responsible for isotopic variations.

Although δ13C- and δ18O-values of stage-I calcite are similar to adjacent stage-II and -III calcite, 87Sr86Sr ratios of adjacent calcite pairs are generally different, indicating that each formed from different fluids or a fluid whose 87Sr86Sr composition varied through time due to mixing.

Isotopic modeling indicates that calcite cap rock formed from either of two fluid mixtures: (1) formation water and meteoric water between 40° and 80°C, the source of light carbon being either thermogenic CH4 or liquid hydrocarbons; or (2) formation water, meteoric water and seawater between 50° and 70°C with thermogenic CH4 being the light carbon source. Sr was contributed by both anhydrite and fluid. Overall, it appears that calcite cap rock formed from top to base from mixtures of formation water, containing isotopically light carbon and heavy oxygen, and seawater and/or meteoric water, containing isotopically heavy carbon and light oxygen. During this progression the contributions of formation water increased at the expense of seawater and/or meteoric water. The correlation between δ18O and δ13C probably indicates that separate fluid pulses had different carbon abundances and/or slightly different δ13C-values.

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