T7 Iron Formations, Ferruginous Sediments, and Redox through Time and Space
Sunday, 22 September 2019
8:00 AM - 12:00 PM
Room 229A, North Building
EXPERIMENTAL EXAMINATION OF IRON PHOTOCHEMISTRY IN ANCIENT OCEANS
Paper number: T7-5
Program: Technical Sessions
Time: 9:00 AM – 9:15 AM
Authors
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Stephen J. RomanielloArizona State University, Tempe, AZ
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Hilairy E. HartnettArizona State University, Tempe, AZ
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A.D. AnbarArizona State University, Tempe, AZ
Abstract
To assess the viability of the photooxidation hypothesis it is necessary to determine the wavelengths of light driving the reaction. Photooxidation of Fe2+ by light 300 - 420 nm was reported in early experiments (Braterman et al., 1983), and predicts a rate of oxidation that can account for BIF deposits. However, subsequent experimental work found no photooxidation above 254 nm (Konhauser et al., 2007), in which case oxidation rates are much lower. Preliminary prior work by our group similarly found no oxidation above 295 nm (Castleberry, 2007). The validity of these studies is unclear because they used Hg lamps which do not realistically simulate the solar spectrum. They are also difficult to compare because they all used different experimental designs and different (and in some cases unrealistic) solution compositions.
Our new work uses a Xe lamp that accurately simulates the solar spectrum, and solution compositions that approximate possible Archean open ocean seawater. We directly measure change in [Fe2+] and [Fe3+] and total [Fe] to completely characterize the fate of dissolved Fe. Preliminary results with full-spectrum light reveal a photooxidation rate of 5.7x10-3 mM Fe/day, which extrapolates to global rates insufficient to account for BIF deposition. The next step is to incorporate spectral cut-off filters to pin-point the range of light driving the reaction, and better quantify its potential importance in different environments.
Geological Society of America Abstracts with Programs. Vol. 51, No. 5
doi: 10.1130/abs/2019AM-340396
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