Subsoil samples from selected North Carolina Ultisols and Brazilian Oxisols were analyzed to determine how the colors of these materials were influenced by the nature and distribution of their constituent iron oxides. The effects of extraneous variables, i.e., other than the iron oxides, were minimized by utilizing pairs of red and yellow soils that were otherwise similar in their physical, morphological, and mineralogical properties.The iron oxides were found to be concentrated in the <0.2‐µm fractions, and the colors of these clays were the same as or similar to those of the parent soils. The spectral properties of the <0.2‐µm clays were primarily influenced by iron mineralogy. Goethite or mixtures of goethite and hematite were identified in all of the clays; however, Mössbauer analyses indicated that the red members of all sample pairs contained larger proportions of hematite than did their yellow counterparts. In addition, as the clays became redder in hue, the ratio of hematite to goethite generally increased. Calculated surface areas for the iron oxides ranged from 60 to 200 m2/g; values from the yellow clays were consistently higher than those obtained from their red counterparts. The yellow clays were also more efficient adsorbers of phosphate.

The mineralogical composition of the surface soil horizon (0-15 cm) of Wahiawa soil (Tropeptic Eutrustox) was investigated by X-ray diffraction (XRD), high gradient magnetic separation (HGMS), transmission electron microscopy (TEM), and infrared methods. The concentration of lithiophorite decreased with particle size and none was present in the clay fraction as indicated by XRD. Lithiophorite was further concentrated from the crushed sand-sized fraction by HGMS. Hexagonal, electron-dense, often twinned lithiophorite particles were identified by electron diffraction. Differential infrared (DIR) spectra obtained by dissolving Mn oxides in acidified hydroxylamine hydrochloride (HAHC) indicated lithiophorite as the HAHC-soluble Mn-phase. Lithiophorite compositiion, as revealed by chemical analysis of the HAHC extracts, consisted of appreciable amounts of Mn, Al, Zn, Co and Mg, and less than stoichiometric amounts of Li. Sodium hydroxide treatment apparently altered the lithiophorite, as revealed by the DIR spectrum of the hydroxylamine-soluble fraction of the NaOH-treated sample compared with the untreated sample. The high crystallinity of the lithiophorite was suggested by its resistance to chemical dissolution and narrow X-ray diffraction lines. No evidence for the presence of todorokite or birnessite was found, contrary to earlier reports. Examination of sand-sized nodules by scanning electron microscopy indicated large (2-5 �m) platy lithiophorite crystals at the surface of these nodules. Electron microprobe analysis of these platy particles indicated iron enrichment near the surface. The freshly fractured nodule surface revealed numerous unaltered platy crystals of lithiophorite filling the veins of the nodule.

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