0024-4902/01/3604- $25.00 © 2001 åÄIä “Nauka /Interperiodica” 0337
Lithology and Mineral Resources, Vol. 36, No. 4, 2001, pp. 337–352. Translated from Litologiya i Poleznye Iskopaemye, No. 4, 2001, pp. 390–407.
Original Russian Text Copyright © 2001 by Drits, Ivanovskaya, Sakharov, Gor’kova, Karpova, Pokrovskaya.
INTRODUCTION
Chlorites form in various geological settings includ-
ing clastic and volcaniclastic rocks, which experienced
postsedimentary transformations, sedimentary and
magmatic rocks, greenschist-facies rocks, altered mafic
and ultramafic rocks, hydrothermally altered rocks,
marine evaporite and carbonate deposits, and others
(Drits and Kossovskaya, 1991). The ideal chlorite
structure is characterized by regularly alternating octa-
hedral brucite and 2 : 1 layers (Bailey, 1988). Based on
the relative position of these layers in the structure,
chlorite occurs as 12 three-dimensional regular poly-
types and 6 semirandom polytypes containing packing
defects related to disordered shift along the b axis by
b/3 (Bailey, 1988; Bailey and Brown, 1962; Zvyagin,
1964). Because of the variety of isomorphous substitu-
tions of the octahedral and tetrahedral cations, the gen-
eral formula of chlorites can be written as follows:
where R
2+
is Fe
2+
and Mg, R
3+
is Fe
3+
and Al cations,
and represents the vacant octahedra.
The wide isomorphism of chlorites simulated the
search of relations between their formation conditions,
structure, and composition (Bailey, 1988; de Caritat
et al., 1993; Drits and Kossovskaya, 1991; Hayes,
1970; Walker, 1993). Particular attention was given to
application of chlorite as geothermometer. Numerous
observations showed that temperature increase, which
is related to increase of burial depth, metamorphic
grade, or heating of solutions in the hydrothermal sys-
tems, causes a systematic decrease in tetrahedral Si and
octahedral vacancies (Battaglia, 1999, Cathelineau,
1988; de Caritat et al., 1993; and others). Based on
R
z
2+
R
y
3+
3- y - z
( 29 S
4- x
Al
x
( 29 O
10
OH ( 29
8
,
chemical analyses and temperatures estimated by dif-
ferent methods, several empirical equations have been
proposed to relate the composition and temperature of
chlorite formation. The review of the works devoted to
chlorite geothermometry is given by de Caritat et al.
(1993).
Chlorites often occur in a mixture with other miner-
als, which hampers the determination of their chemical
composition. Therefore, the relations between compo-
sition and unit cell parameters of chlorites have been
studied (Shirozu, 1958; Brindley, 1961; Kepezhinskas,
1965; Bailey, 1975, 1988). Drits and Smoliar-Zvyagina
(Drits and Smoliar-Zviagina, 1992) showed that coor-
dinates of atoms in the unit cell can be deduced from
the chemical composition and b parameter.
Because of wide abundance of chlorites in different
conditions, special attention has been given to the study
of structural mechanism of their formation (Bailey,
1988; Buseck and Veblen, 1988; Drits and Koss-
ovskaya, 1991). High-resolution transmission electron
microscopy (HRTEM) made it possible to solve this
problem at a new level (Banfield and Bailey, 1996;
Banfield et al., 1994; Buseck and Veblen, 1988; Eggle-
ton and Banfield, 1985). It was shown that the chlorite
structure formed by solid-state reaction inherits struc-
tural elements of the parental rock-forming silicates
affected by weathering, methamorphism, or hydrother-
mal alterations. Of interest in this respect are the works
on transformations of biotite into chlorites (Buseck and
Veblen, 1988; Olives and Amouric, 1984; Veblen and
Ferry, 1983), serpentine into chlorite, and chlorite into
serpentine (Banfield and Bailey, 1996; Banfield et al.,
1994). In particular, it was shown that the transforma-
tion of serpentine into chlorite is mainly accompanied
Pseudomorphous Replacement of Globular Glauconite
by Mixed-Layer Chlorite–Berthierine in the Outer Contact
of Dike: Evidence from the Lower Riphean Ust’-Il’ya Formation,
Anabar Uplift
V. A. Drits, T. A. Ivanovskaya, B. A. Sakharov, N. V. Gor’kova, G. V. Karpova,
and E. V. Pokrovskaya
Geological Institute (GIN), Russian Academy of Sciences, Pyzhevskii per. 7, Moscow, 109017 Russia
Received February 12, 2001
Abstract—Globular, platy, and fine-dispersed phyllosilicates of chloritic composition were studied in the outer
contact of dike with glauconite-bearing rocks. It is shown that the globular Al-glauconite is replaced by pseudo-
morphs of mixed-layer Mg- and Fe-bearing chlorite–berthierine containing 5% berthierine layers in this zone.
The crystallochemical characteristics and microstructure are reported for the globular, platy, and fine-dispersed
chlorites. The possible models of chlorite–berthierine formation are discussed.