[1] The well defined composition of the Comanche rock's carbonate (Magnesite 0.62 Siderite 0.25 Calcite 0.11 Rhodochrosite 0.02 ) and its host rock's composition, dominated by Mg-rich olivine, enable us to reproduce the atmospheric CO 2 partial pressure that may have triggered the formation of these carbonates. Hydrogeochemical one-dimensional transport modeling reveals that similar aqueous rock alteration conditions (including CO 2 partial pressure) may have led to the formation of Mg-Fe-Ca carbonate identified in the Comanche rock outcrops (Gusev Crater) and also in the ultramafic rocks exposed in the Nili Fossae region. Hydrogeochemical conditions enabling the formation of Mg-rich solid solution carbonate result from equilibrium species distributions involving (1) ultramafic rocks (ca. 32 wt% olivine; Fo 0.72 Fa 0.28 ), (2) pure water, and (3) CO 2 partial pressures of ca. 0.5 to 2.0 bar at water-to-rock ratios of ca. 500 mol H2O mol À1 rock and ca. 5 C (278 K). Our modeled carbonate composition (Magnesite 0.64 Siderite 0.28 Calcite 0.08 ) matches the measured composition of carbonates preserved in the Comanche rocks. Considerably different carbonate compositions are achieved at (1) higher temperature (85 C), (2) water-to-rock ratios considerably higher and lower than 500 mol mol À1 and (3) CO 2 partial pressures differing from 1.0 bar in the model set up. The Comanche rocks, hosting the carbonate, may have been subjected to long-lasting (>10 4 to 10 5 years) aqueous alteration processes triggered by atmospheric CO 2 partial pressures of ca. 1.0 bar at low temperature. Their outcrop may represent a fragment of the upper layers of an altered olivine-rich rock column, which is characterized by newly formed Mg-Fe-Ca solid solution carbonate, and phyllosilicate-rich alteration assemblages within deeper (unexposed) units.