Affiliation:
1. School of Earth, Environment and Society, Bowling Green State University, Bowling Green, OH 43403, USA
Abstract
Iron oxide assemblages are central to many pursuits, ranging from Mars exploration to environmental remediation. Oxides and oxyhydroxides of iron both carry the special properties of color and magnetism. In this paper, we use visible-light spectroscopy and rock magnetic data collected at varying temperatures (~77–973 K) to analyze the concentrations and identities of iron oxides found in natural hematite-dominated samples that were obtained from a scientific drill core of Late Triassic red beds in the American Southwest. Our results suggest that hematite colorization of Earth materials varies from red to blue/purple as crystal size increases. Second-derivative analysis of the collected visible-light spectra allows this variation to be measured through the characteristic wavelength band position. Magnetic coercivity data indicate “hardness” differences that also may suggest smaller grain sizes are associated with redder colors. Yellowish maghemite and goethite have overlapping characteristic wavelength band positions that make it challenging to distinguish their contributions to mixed assemblages from visible-light data alone. Remanent magnetizations acquired at ~77 K and room temperature suggest the presence of hematite and a low-coercivity phase that may be maghemite and/or oxidized magnetite. However, we interpret this phase as maghemite in order to explain the changes in iron oxide concentrations indicated by visible-light intensities near ~425 nm and because the thermal demagnetization data suggest that goethite is absent from the samples. Future research that increases the resolution of hematite, maghemite, and goethite detection in experimental and natural samples will provide opportunities to refine the study of past climates and constrain soil iron availability under future changes in global moisture and temperature. Multimethod datasets improve understanding of environmental conditions that cause iron oxides assemblages to shift in phase dominance, grain size, and crystallinity.
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