Paragenetic, textural, and chemical characteristics of columbite-tantalite
minerals are examined as steps towards identifying the metallogenetic proce
sses of their host granitoids. Columbite-tantalite-bearing granitoids of th
e Eastern Desert province of Egypt can be categorized into: (i) metaluminou
s alkali granites; (ii) peraluminous Li-albite granites; and (iii) metasoma
tized biotite and/or muscovite granite (i.e. apogranites).
Columbite of the alkali granite is of FeNb2O6 composition and associated wi
th annite. The low F and Li contents of the associated mica precludes the i
mportant role of these volatile elements during the late stage of evolution
of the alkali granites, thus delaying fractionation of Mn over Fe and Ta o
ver Nb.
Compositionally, columbite-tantalite of the Li-albite granites is constrain
ed between MnNb2O6 and MnTa2O6 (the Ta/(Nb+Ta)(atom) ratio ranges between 0
.10 and 0.80). This low to high ratio and the association of columbite-tant
alite with topaz, fluorite and lithian micas (in the series zinnwaldite-whi
te mica) indicate a higher solubility for Ta-fluoride complex compounds and
their more stabilized state at lower temperatures in Li- and F-rich sodic
melts. The columbite-tantalite commonly exhibits a mottled or patchy zoned
texture with the rims consistently higher in Ta than the cores, reflecting
the later effect of a corrosive supercritical vapour phase.
The columbites of metasomatized granites range in composition between FeNb2
O6 and MnNb2O6. They are characterized by high Ti and U, and low Ta content
s (the Ta/(Nb+Ta)(atom) ranges between 0.01 and 0.15), indicating depositio
n from alkaline (K+, Na+ -rich), and relatively high-temperature interactin
g fluids. However, the Mn-enriched columbites are commonly encountered in t
he apical parts of the apogranites and formed in response to high mu(KF); a
nd mu(LiF) required for stabilizing the associated Li-siderophyllite or zin
nwaldite. Columbites of the apogranites commonly exhibit progressive (eithe
r normal or reverse) zoning which can be attributed to the disequilibrium c
onditions (e.g. sudden change in the pH) between the growing crystal and th
e solutions.