H. Vali et al., SMECTITE-GROUP MINERALS IN DEEP-SEA SEDIMENTS - MONOMINERALIC SOLID-SOLUTIONS OR MULTIPHASE MIXTURES, The American mineralogist, 78(11-12), 1993, pp. 1217-1229
Results of XRD, TEM, and chemical analyses are combined to characteriz
e the true chemistry and structural formula of the smectite-group mine
rals present in selected samples of deep-sea sediments from the north-
central Pacific and Angola, Lau, and North Fiji Basins. In most cases,
the abundant Fe and K in the <0.2-mum fraction is associated with acc
essory minerals such as mica, phillipsite, and iron oxides. Bulk analy
tical data obtained from the <0.2-mum fraction, corrected for the pres
ence of these minerals, reveal a structural formula very close to that
of ideal montmorillonite. The extensive chemical variability among me
mbers of the clay-mineral group usually is attributed to the occurrenc
e of solid solution. The variability in smectite-group minerals also c
ould be due to (1) the occurrence of mixed-layer structures, (2) the p
resence of compositionally distinct domains in the structure, or (3) a
mixture of two or more distinct phases. A clear distinction between a
monomineralic solid-solution phase and a mixture of coexisting end-me
mbers based on chemical composition or even conventional XRD and HRTEM
techniques is of crucial importance. The data presented in the litera
ture concerning the nature of the smectite-group phase and related I/S
mixed layers do not necessarily reflect the true nature of the indivi
dual clay-mineral phases. The application of the term ''smectite'' to
a material characterized by a structural formula should be avoided.