Modeling Calcium Sulfate Chemistries with Applications to Mars

1G.M. Marion, 2D.C. Catling, 3J.S. Kargel, 4J.K. Crowley
1Desert Research Institute, 2215 Raggio Parkway, Reno, NV 89512, USA.
2Department of Earth & Space Sciences, University of Washington, Seattle, WA 98195, USA.
3Department of Hydrology & Water Resources, University of Arizona, Tucson, AZ 85721, USA.
4P.O. Box 344, Lovettsville, VA 20180, USA.

On Mars, evidence indicates widespread calcium sulfate minerals. Gypsum (CaSO4•2H2O) seems to be the dominant calcium sulfate mineral in the north polar region of Mars. On the other hand, anhydrite (CaSO4) and bassanite (CaSO4•0.5H2O) appear to be more common in large sedimentary deposits in the lower latitudes. The tropics are generally warmer and drier, and at least locally show evidence of acidic environments in the past. FREZCHEM is a thermodynamic modeling tool used for assessment of equilibrium involving high salinity solutions and salts, designed especially for low temperatures below 298 K (with one version adapted for temperatures up to 373 K), and we have used it to investigate many Earth, Mars, and other planetary science problems. Gypsum and anhydrite were included in earlier versions of FREZCHEM and our model Mars applications, but bassanite (the CaSO4 hemihydrate) has not previously been included. The objectives of this work are to (1) add bassanite to the FREZCHEM model, (2) examine the environments in which thermodynamic equilibrium precipitation of calcium sulfate minerals would be favored on Mars, and (3) use FREZCHEM to model situations where metastable equilibrium might be favored and promote the formation or persistence of one of these phases over the others in violation of an idealized equilibrium state.

We added a bassanite equation based on high temperatures (343 to 373 K). A Mars simulation was based on a previously published Na-Ca-Mg-Cl-SO4 system over the temperature range of 273 to 373 K. With declining temperatures, the first solid phase under equilibrium precipitation is anhydrite at 373 K, then gypsum forms at 319 K (46 °C), and epsomite (MgSO4•7H2O) at 277 K. This sequence could reflect, for example, the precipitation sequence in a saturated solution that is slowly cooled in a deep, warm aquifer.

Because FREZCHEM is based on thermodynamic equilibrium, a crude approach to problems involving metastable equilibria is available by removing phases that may have kinetically inhibited formation. Removing anhydrite allows bassanite to precipitate at 373 K, followed by gypsum at 351 K (78 °C), and epsomite at 277 K. Removing anhydrite and gypsum allows bassanite to form from 373 to 273 K. But bassanite formation from warm to cold temperatures does not seem appropriate for Mars and Earth.

An explanation for spatial patterns of gypsum, anhydrite, and bassanite on Mars and Earth could be past environmental differences. Anhydrite and bassanite are favored near Mars’ equator with higher temperatures, along with drier, more saline, and more acidic environments. Gypsum would be favored at the lower temperatures in the Mars polar region with wetter, lower salinity, and less acidic environments. On Earth, Ca-sulfate would likely over time largely finish re-precipitating as the more insoluble gypsum. But Mars was not in long-term moderate climates compared to Earth that strongly influenced the dominance of gypsum on Earth. So while temperature and water/acid environments for CaSO4 minerals on Mars may have been a major factor for these precipitations, the short-term moderate climates on Mars may also have influenced the prevalence of higher soluble CaSO4 species in the lower Mars latitudes.

Reference
Marion GM, Catling DC, Kargel JS, Crowley JK (2016) Modeling Calcium Sulfate Chemistries with Applications to Mars. Icarus (in Press)
Link to Article [doi:10.1016/j.icarus.2016.05.016]
Copyright Elsevier

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