8 Advancing Mineral Science and Exploring Planetary Surfaces: In Honor of MSA Dana Medalist, Elizabeth B. Rampe, Part I
This session honors MSA Dana Medalist Elizabeth B. Rampe, celebrating her contributions to Martian mineralogy and planetary science. We invite studies on in-situ and orbital planetary observations, lab/field data integration, and analog materials for extraterrestrial exploration.Sarah Simpson
Sunday, 19 October 2025
8:00 AM - 12:00 PM
HBGCC, 214C
Oxidative Alteration of Siderite to Goethite and Akaganeite By Chlorate & Bromate: Implications for Recent Siderite Discovery at Gale Crater on Mars.
Paper number: 8-5
Program: Technical Sessions
Time: 9:10 AM – 9:25 AM
Authors
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Lauren MaleskyUTSA, San Antonio, TX
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Michael ThorpeNASA Goddard Space Flight Center CRESST II, Greenbelt, MD
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Ana StevanovicUTSA, San Antonio, Texas
Abstract
Ferrous iron carbonate, siderite [FeIICO3], was discovered in the sulfate-rich Mirador formation at Gale crater. The discovery of pure siderite of high crystallinity likely represents a transition event in the iron and carbon geochemical cycle on Mars. Other ferric minerals detected with siderite likely formed by later diagenetic events. The relatively uncommon presence of siderite and other carbonate minerals on Mars has been hypothesized to be due to acid dissolution. Similarly, an acid alteration hypothesis was suggested to explain the juxtaposition of ferrous and ferric minerals in Gale crater sediments. Here, we conduct laboratory experiments in a closed system environment to determine if acidic dissolution alone and oxyhalogen brines could weather siderite to produce ferric oxyhydroxide in different Mars-relevant fluids at ambient conditions (24°C, 1 atm).
We designed laboratory experiments to evaluate the oxidative weathering of siderite at Gale crater as a function of oxidant type [NaClO3 and NaBrO3], background fluid composition [MgCl2 and MgSO4], pH (~2.5, 4.5, and 7), and time [35 and 100 days]. All experiments were conducted inside an anaerobic chamber (N2 = 97%, H2 = 3%; O2 < 1 ppmv). The 50 mL glass serum bottle reactors used in the experiments were wrapped in Al foil to prevent any inadvertent influence of ultraviolet radiation on siderite dissolution and oxidation. 50 mL solutions containing 0.2 g siderite (~4 g L-1; W:R ~ 250) were allowed to react for about 100 days with ~100 mmol L-1 NaClO3 or NaBrO3. At the end of the experiments, all reactors were filtered, final solution pH was measured, and the filtrates and the supernatant fluids were analyzed by a suite of analytical instruments.
Contrary to popular hypothesis, siderite survived extensive acidic diagenesis. On the other hand, chlorate- and bromate-containing experimental solutions were able to substantially alter siderite in all types of fluid conditions, including near-neutral solutions. The primary product of alteration was found to be goethite and akaganeite forming in acidic Cl-rich fluids. Chlorate and bromate can oxidatively weather siderite to form ferric hydroxide minerals, similar to those observed at Gale crater, Mars. We propose a top-down alteration model to explain the iron mineralogy in the sulfate-rich section at Gale crater, and our ongoing experiments at lower temperatures (4 and 0°C) will be able to investigate siderite alteration as a function of temperature.
Geological Society of America Abstracts with Programs. Vol. 57, No. 6
doi: 10.1130/abs/2025AM-414702
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