INTERCRYSTALLINE CATION PARTITIONING BETWEEN MINERALS OF THE TRIPLITE-ZWIESELITE-MAGNIOTRIPLITE AND THE TRIPHYLITE-LITHIOPHILITE SERIES IN GRANITIC PEGMATITES
P. Keller et al., INTERCRYSTALLINE CATION PARTITIONING BETWEEN MINERALS OF THE TRIPLITE-ZWIESELITE-MAGNIOTRIPLITE AND THE TRIPHYLITE-LITHIOPHILITE SERIES IN GRANITIC PEGMATITES, Contributions to Mineralogy and Petrology, 118(3), 1994, pp. 239-248
Minerals of the triphylite-lithiophilite, Li(Fe, Mn)PO4, and the tripl
ite-zwieselite-magniotriplite series, (Mn, Fe, Mg)(2)PO4F, occur in th
e fate stage period of pegmatite evolution. Unfortunately, neither are
the genetic relationships between these phosphates fully understood n
or are thermodynamic data known. Consequently, phosphate associations
and assemblages from 8 granitic pegmatites - Clementine II, Rubicon II
and III, and Tsaobismund (Namibia); Hagendorf-Sud and Rabenstein (Ger
many); Valmy (France); Viitaniemi (Finland)- have been tested for comp
ositional zoning and intercrystalline partitioning of main elements by
electron microprobe techniques. Although the selected pegmatites disp
lay varying degrees of fractionation, and the intergrowth textures ind
icate different genetic relationships between the phosphates, the plot
s of mole fractions X(Fe) = Fe/(Fe + Mn + Mg + Ca), X(Mn) = Mn/ (Fe Mn + Mg + Ca), and X(Mg) = Mg/(Fe + Mn + Mg + Ca) can be fitted relati
vely well with smooth curves in Roozeboom diagrams. Their deviations f
rom symmetrical distribution curves are mainly dependent upon X(Mg) or
X(Ca), and upon non-ideal solutions. Surprisingly small differences b
etween the partition coefficients were detected for intergrowths of di
fferent origin. However, the partitioning of shared components among c
oexisting phases is clearly dependent upon the conditions of formation
. Compositional zoning is observed only when both Fe-Mn phosphates are
intergrown mutually or with other Fe-Mn-Mg mineral solid-solutions. T
hus, the zoning does not seem to be due to continuous crystallization,
but to later diffusion processes. The triplite structure has preferen
ce for Mn, Mg, and Ca, while Fe prefers minerals of the triphylite ser
ies. A quantification of main element fractionation between minerals o
f the triphylite and the triplite series is possible in the cases wher
e diffusion can be excluded. For the Fe/(Fe + Mn) ratios of core compo
sitions an equation with a high correlation coefficient (R = 0.988) wa
s determined: Fe/(Fe + Mn)(Tr) = [Fe/(Fe + Mn)(Li)]/{2.737 - (1.737)[F
e/ (Fe + Mn)(Li)]} (Tr = triplite series, Li = triphylite series). Con
sequently, the Fe/(Fe + Mn) ratio of the triplite series can now also
be used in the interpretation of pegmatite evolution, just like that o
f the triphylite series which has been successfully applied in the pas
t.