High-Mn (up to 9.5 wt %MnO) monticellite was first detected in the dee
p-seated carbonatites of the Oka Complex, Quebec. The Physical propert
ies (refractive indices, density), interplanar spacings, unit-cell par
ameters (a(0) = 6.440, b(0) = = 11.100, c(0) = 4.840), and chemical co
mposition (Ca-1.01(Mg0.48Fe0.302+Mn0.21)(0.99)Si1.00O4.00) of this min
eral arec intermediate between analogous values for minerals of the mo
nticellite group: CaMgSiO4 (monticellite), CaFeSiO4 (kirschsteinite),
and CaMnSiO4 (glaucochroite). Our data and preexisting data on melt an
d fluid inclusions in monticellite and associated minerals indicate th
at the following: (1) the monticellite-calcite carbonatites were gener
ated from heterogeneous (melt + fluid) magmatic systems; (2) the cryst
allization temperatures of monticellite in the deep-seated carbonatite
complexes are higher (up to 890 degrees C) than those of volcanic roc
ks (600-700 degrees C), and (3) the monticellite sodiccarbonatite of t
he Oldoinyo Lengai were formed at a temperature no more than 550 degre
es C; (4) the fluid pressure under which the Oka carbonatite was forme
d is estimated at 4.6 kbar. The data reported in this paper suggest th
at monticellite is stable only under low pressures.