Abstract:
The farm Maandagshoek 254 KT is situated in the
eastern lobe of the Bushveld Complex. The investigated
sequence forms part of the Winterveld Norite-Anorthosite of
the critical zone and consists of the UGl, UG2, UG3 and
UG3A cyclic units. These cyclic units consist of a basal
chromitite with or without olivine, overlain successively
by melanorite, norite, and leuconorite to an anorthosite
layer above. The cyclic units are punctuated by sharp
contacts and a remarkable persistence along strike and dip.
The En content of orthopyroxene and the An content
of plagioclase decrease and increase respectively upwards
through the UGl and UG2 cyclic units. Breaks in this trend
occur below the chromitite layers where the En content of
bronzite increases and in the anorthosite layers at the
top of the cyclic units where the An content of plagioclase
increases. A trace element study showed Rb and Zr to increase
upward in the UGl and UG2 cyclic units. Rb and Sr display
a reasonable antipathetic relationship. The Cr and Ni
content of the orthopyroxenes increases upwards irregularly
in the cyclic layers, but the Ni content decreases where
visible sulphides are present. Cu, Ni and the platinoid
elements increase in the chromitite layers, especially the
UG2 chromitite layer. Clinopyroxene is not commonly cumulus
and is identified as chromi~_ferous augite. The equilibrium
temperature of a coexisting orthopyroxene-clinopyroxene pair
was calculated according to the Wood-Banno and Wells modifications
to be 1179°c and 1097°c respectively. Cumulus
olivine associated with the UG2 pegmatoid and the UG3A chromitite
was identified as chrysolite. The compositions of 15 chromite
samples were determined and showed similar chemistry to those
reported by De Waal (1975). The crystallization temperatures
of coexisting olivine and chromite pairs was determined using the Jackson (1969) and Roeder et al, (1979)
geothermometers.
The UG2 chromitite layer contains an average of
8,5 g/t PGE and Au over a width of 0,64 metres in 22
intersections in borehole and underground samples. A
study of the distribution of Pt and Pd in the weathered
and unweathered zones clearly shows that both, but especially
Pd, are mobile and depleted in the surface environment.
The sulphide liquid in the UG2 chromitite layer was calculated
to have contained 925 ppm Pt and 934 ppm Pd which is 578 and
359 times respectively the calculated levels in early
immiscible sulphide liquids (Naldrett and Cabri, 1976).
A model is proposed in which the UG2 chromitite layer acted
as a physico-chemical barrier to the upward migrating late
deuteric fluids and volatiles charged with platinoids, Au,
Sb, As and Te. The platinoids were collected by earlier
sulphide droplets which separated from the magma during
crystallization of the UG2 chromitite layer.
Structures are sub-divided into Class I and Class II
features. Class I features are related to viscosity and
density contrasts of layers at the time of crystallization
of the magma and may be seen as bifurcating and anastomosing
layers, folding and slump features, rafting of chromitite
blocks, minor faults and potholes. Class II features are
associated with tectonic movement which postdates the
consolidation of the layering and are sub-divided into
three categories; faults, dolerite dykes and pipes. The
pipes are pegmatoidal in character, zoned with ultramafic
cores and pyroxenite rims, have sharp contacts and cause
downwarping and attenuation of the layering towards the
pipes to form marginal synclines. It is postulated that intercumulus material coalesced along structural weaknesses
and moved upward until the lithostatic pressure impeded
upward movement at which time lateral and outward intrusions
occurred. The layers of the intruded rocks bent down to
accommodate the outward flowing material and gave rise to
the marginal synclines.
The concept of a closed cell cyclic unit is introduced
to account for the inherent characteristics and origin of
the cyclic units of the upper chromitite group.