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Abstract

Aragonite (CaCO3) is a stable calcium carbonate phase under high pressure conditions. However, its formation in (sub)surface environments, where calcite is the stable polymorph, is widespread. Regardless of its origin, aragonite is expected to undergo transformation into calcite under moderate pressures and temperatures. However, this transformation does not always take place, which results in the presence of abundant aragonitic relics in the geological record. Traditionally, this preservation has been explained by the presence of chemical inhibitors that prevent the conversion of aragonite to calcite. While it is widely accepted that magnesium (Mg) plays a key role in the polymorphic selection of CaCO3, the influence of other ions has also been suggested. This work evaluates the effect that different concentrations of sulfate (SO42−) in the fluid has on the progress of the aragonite-to-calcite transformation at 220 °C. Our results show that, upon reaction with deionized water or sulfate-poor solutions ([SO42−]aq < 0.1 mM), aragonite single crystals are extensively replaced by calcite aggregates (crystal size > 15 µm) through an interface coupled dissolution-precipitation reaction. The replacement starts at the aragonite crystal surfaces and advances inwards thanks to the development of an extensive network of fractures. Contrarily, when the solution bears higher concentrations of sulfate ([SO42−]aq > 0.1 mM), only a thin layer of smaller crystals of calcite (< 10 µm) form on the aragonite substrates, without any further transformation taking place. We interpret that these smaller crystals exert too little crystallization pressure and fail to promote the development of a network of fractures. In the absence of this network, the aragonite-calcite transformation cannot take place. The transformation does not occur neither when the experiments are conducted with deionized water and fragments of gypsum or anhydrite together with the aragonite grains. The results of this study shed light on the influence of dissolved sulfate in the kinetics of the fluid-driven transformation of aragonite into calcite. These results are useful to understand the preservation of aragonite in a variety of current geological settings and provide valuable insights for better understanding the diagenesis of sedimentary carbonates.