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A synthesis of systematic mineralogy

Department of Geology, University of Georgia, Athens, Georgia 30602-2501, U.S.A.

Correspondence: ^* E-mail: rlsbk{at}gly.uga.edu

This paper presents several new diagrams that document previously unappreciated patterns and predictability in systematic mineralogy. They illustrate, for example, that sulfide minerals of single cations contain only intermediate to soft cations (cations with at least some outer-shell electrons). On the other hand, hard cations (those with no outer-shell electrons) only enter into a few sulfide minerals, all of which also contain intermediate cations. Among the simple chloride, fluoride, oxide, and carbide minerals of hard cations, ionic potential (charge/radius) of cations is proportional to that of anions (e.g., from KCl to SiC). Among the simple nitrate, sulfate, carbonate, phosphate, and silicate minerals of hard cations, ionic potential of inter-radical cations is inversely proportional to the ionic potential of the cations in the oxysalt radical (e.g., from KNO₃ to ZrSiO₄). Across both of these sets of minerals, non-simple minerals (H₂O- and OH--bearing minerals or minerals with extra O^2–) in each group typically involve cations of higher ionic potential than those of the simple minerals. The result is predictability and pattern in the compositions of minerals.

This article has been cited by other articles:

				L. B. Railsback Patterns in the compositions of oxysalt and sulfosalt minerals, and the paradoxical nature of quartz American Mineralogist, February 1, 2007; 92(2-3): 356 - 369. [Abstract] [Full Text] [PDF]