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Fig. 10.8 Course of
crystallization of liquid
in the join diopside -
nepheline - leucite (after Gupta
and Lidiak 1973)
1275 ± 5 C
o
Fo
Di
Ne
Lc
1194 ±5 o
Lc
Fo
o
(Ne-Lc-Fo-Mel)
1180 ± 5 C
1257±5 C
o
Fo
Di
Lc
Ne
Lc
Fo
(Fo-Di-Lc-Mel)
Mel
Mel
(1168C -1100C)
o
o
(Fo-Di-Lc-Mel-Ne)
o
o
(Fo out, 1135 C -1060 C)
Mel
Ne
Lc
Di
Fig. 10.9 Rock-
nomenclature diagram,
corresponding to Fig. 10.8
(after Gupta and Lidiak
(1973)
1275 ±5 o
1194 ±5 o
1180±5 o
1257±5 o
Olivine-Melilite-
Nepheline Leucitite
o
o
(1168C-1100C)
buffer conditions in a furnace, where oxygen fugacity was maintained by passing a
mixture of gases having compositions, CO 2 :95.25%andCO:4.75%.Theystudied19
compositions to determine phase relations and course of crystallization of an oliv-
ine
leucitite and a katungite liquid. They concluded that both the two
magma types yield an olivine
nepheline
-
-
Cunder
atmospheric pressure and under QFM buffer condition. They noted a reaction rela-
tionship between olivine and liquid, and found that olivine
melilite
nepheline leucitite liquid at 1,090
°
-
-
finally disappears at around
1,053
C. The course of crystallization of liquid as established by Gee and Sack (1988)
is similar to what was predicted by Gupta et al. (1973; Figs. 10.8 and 10.9 ).
They found cotectic crystallization of leucite + nepheline + spinel
°
±
meli-
lite
±
high calcium pyroxene
±
olivine (
±
whitlockite
±
perovskite) in equilibrium
with liquid at 1 atm (fO 2 *
QFM) over the temperature range, 1,050
-
1,110
°
C.
 
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