Jm. Ferry, 3 NOVEL ISOGRADS IN METAMORPHOSED SILICEOUS DOLOMITES FROM THE BALLACHULISH AUREOLE, SCOTLAND, The American mineralogist, 81(3-4), 1996, pp. 485-494
Isograds were mapped in siliceous dolomites from the Ballachulish aure
ole on the basis of the formation of geikielite (MgTiO3), baddeleyite
(ZrO2), and qandilite (Mg2TiO4) by the following model reactions: ruti
le + dolomite = geikielite + calcite + CO2, zircon + 2 dolomite = badd
eleyite + forsterite + 2 calcite + 2 CO2, and geikielite + periclase =
qandilite. The (T, X(CO2)) conditions of reaction inferred from (1) m
ineral equilibria in pelitic rocks, (2) calcite + dolomite thermometry
, and (3) the diopside + dolomite + forsterite + calcite + tremolite a
nd dolomite + periclase + calcite equilibria are: geikielite isograd (
640-655 degrees C, 0.76-0.80); baddeleyite isograd (660-710 degrees C,
0.76-0.95); qandilite isograd (725-755 degrees C, <0.08). These T-X(C
O2) conditions for the geikielite and baddeleyite isograds are the sam
e within error of those independently estimated from rutile + dolomite
+ geikielite + calcite and zircon + dolomite + baddeleyite + forsteri
te + calcite equilibria using Berman's thermodynamic data base. Rutile
, zircon, geikielite, and baddeleyite are common in dolomites from at
least two other contact aureoles in Scotland and Montana. Although the
minerals occur in concentrations <0.01%, they appear to have been in
local equilibrium during metamorphism both with each other and with co
existing carbonates and silicates and are potentially useful but curre
ntly unexploited records of the physical conditions of metamorphism.