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Geology of the B Lode, A
Lode and 1 Lens on CML7,
Broken Hill, N.S.W.
Richard B. Tully
Honours Research Report submitted as part of the B.Sc.(Hons) degree in the
School of Earth Sciences, University of Melbourne
Submitted on October 31st, 2002
Chapter Two – Broken Hill Geology
Chapter Two - Broken Hill Geology
2.1 Regional Geology 2.1.1 Stratigraphy
The stratigraphy of the Broken Hill Block (Figure 2.1) described by Stevens et al. (1980,
1988) and by Willis et al. (1983) is still currently generally supported in the literature
including Parr and Plimer (1993), Laing (1996), Stevens and Burton (1998) and Walters
(1998). Due to an intense, prolonged metamorphic and deformation history at Broken Hill,
the recognition of lithological protoliths is exceedingly difficult. As a consequence, there
have been some studies that have disputed parts of the interpreted stratigraphy (e.g.
Haydon and McConachy, 1987; Wright et al., 1987; Vassallo and Vernon, 2000). In light
of new studies, the interpreted stratigraphy of the Willyama Supergroup in proximity of the
orebodies needs constant re-evaluation.
Figure 2.1: Stratigraphy of
the Willyama Supergroup
described by Willis et al.
(1983), also highlighting the
depositional trends and
occurrence of mineralisation
and exhalative sediments
(after Parr and Plimer, 1993).
5
Chapter Two – Broken Hill Geology
Regional mapping by the New South Wales Geological Survey was instrumental in
the re-classification of the Willyama Supergroup (Willis et al., 1983) into smaller “rock
type associations” called suites (Stevens et al., 1980). The lowest suite of the Willyama
Supergroup identified is the Clevedale Migmatite, followed by the Thorndale Composite
Gneiss, although recently classified units, the Redan Gneiss, Ednas Gneiss and Mulculca
Formation (Stevens et al., 1988) in the south-east of the Broken Hill Block are thought to
occur stratigraphically beneath or equivalent to the Clevedale Migmatite and Thorndale
Composite Gneiss. Overlying these is the Thackaringa Group, which is followed by the
Broken Hill Group, the Sundown Group and the uppermost sequence, the Paragon Group
(Table 2.1). The principal trend is from the quartzo-feldspathic rich lithostratigraphic
sequences of the Thackaringa Group, through the mineralised and exhalative
lithstratigraphic sequences of the Broken Hill Group, to the metasediment-rich sequences
of the Sundown and Paragon Groups (Parr and Plimer, 1993).
Table 2.1.1a: Lithostratigraphic units of the Willyama Supergroup and their interpreted protoliths.
Stratigraphic
Name
Suite
Unit Lithology Interpreted Protolith
Clevedale Migmatite > 500m
1
Poorly bedded feldspathic gneiss, migmatite
metasediment and minor amphibolite (Stevens
et al., 1980).
Detrital sediments containing volcanic detritus
and ash fall tuffs (Stevens et al., 1988).
Thorndale Composite Gneiss 1000m
2
Thinly to poorly bedded metasedimentary and
quartzo-feldspathic composite gneiss and
amphibolite (Stevens et al., 1980)
Fluvial-deltaic feldspathic sand deposition
(Stevens et al., 1988).
Thackaringa Group 1500m
3
Lady Brassey 3.1 Na-plagioclase-quartz rocks (Stevens et al.,
1988).
Na volcanics or air fall tuffs altered by alkaline
lake or seawater (Stevens et al., 1988).
Alma Gneiss 3.2 Coarse grained granitic rock with K feldspar
megacrysts (Willis et al., 1983)
Rhyodacitic lava-flows or ash-flow tuffs (Stevens
et al., 1988) or granitoid intrusion (Vassallo and
Vernon, 2000).
Alders Tank Formation
3.3-
3.4
Metasedimentary and quartzo-feldspathic
composite gneiss (Stevens et al., 1988).
Deep-water turbidite fans or deltaic and
lacustrine deposits (Stevens et al., 1988).
Cues Formation 3.5
Metasedimentary composite gneiss and
metasediments with leucocratic, garnet-biotite
and basic gneisses (Stevens et al., 1988).
Deep-water turbidite fans or deltaic lacustrine
deposits (Stevens et al., 1988).
Himalaya Formation
3.6-
3.9
Na-plagioclase-quartz rocks (Stevens et al.,
1988).
Na volcanics or air fall tuffs altered by alkaline
lake or seawater (Stevens et al., 1988).
Rasp Ridge 3.10 Quartzo-feldspathic gneiss (Stevens et al.,
1980).
Rhyodacitic lava-flows or ash-flow tuffs (Stevens
et al., 1988) or granitoid intrusion (Vassallo and
Vernon, 2000).
6
Chapter Two – Broken Hill Geology
Broken Hill Group 500m
4
Allendale Metasediments
4.1-
4.3
Feldspar-rich and quartz-rich psammitic
metasediments (Stevens et al., 1988).
Deep-water turbidite fans or deltaic and
lacustrine deposits (Stevens et al., 1988).
Parnell Formation
4.4
Amphibolite/basic granulite, garnetiferous
quartzo-feldspathic gneiss and quartz-
garnet/quartz-gahnite rock (Stevens et al.,
1988).
Bimodal rhyodacite-tholeiitic basalt volcanism
with associated exhalites (Stevens et al., 1988) or
marine transgression sequence with storm surge
layers (Wright et al., 1987).
Freyers Metasediment
4.5-
4.6
Well-bedded metasediments of pelitic to
psammitic composition. Offshore marine turbidite or shallow storm/wave base sequence (Stevens et al., 1988).
Hores Gneiss 4.7
Garnetiferous quartzo-feldspathic gneiss and
intercalated metasediments (Stevens et al.,
1988).
Felsic volcanic or volcaniclastic rock (Willis et
al., 1983; Stevens et al., 1988) or arkose
sandstone (Haydon and McConachy, 1987;
Wright et al., 1987).
Silver King Formation
4.8 Massive amphibolites intercalated with
metasediments (Stevens et al., 1988).
Mass flow acid volcanics with intercalated shelf
muds and silts (Stevens et al., 1988).
Sundown Group 1000m
5
Thin bedded pelitic to psammopelitic
metasediments and minor calc-silicates
(Stevens et al., 1980).
Diagenetic carbonate and turbiditic sedimentation
in a marine environment (Stevens et al., 1988) or
sag phase rift-fill sedimentation (Parr and Plimer,
1993).
Paragon Group >2200m
6-8
Well bedded to laminated fine-grained pelitic
schists and psammitic metasediments with
abundant graphitic metasediment (Stevens et
al., 1980).
Deep marine turbidite sequence or shallow
storm/wave base shelf sequence (Stevens et al.,
1988).
2.1.2 Age and Metamorphic History
The Broken Hill Block has undergone a long and intense metamorphic history (Table 2.2).
As a result, precise dating of the Willyama Supergroup stratigraphic units is problematic,
linked to the polymetamorphic history at Broken Hill, with resetting of zircons common
during metamorphism.
Early studies of the Broken Hill Block broadly confined the age of deposition to
1820±100 Ma (Pidgeon, 1967) after the separation of the crust from the mantle at 2100-
2300 Ma (McCulloch and Hensel, 1984). This has recently been constrained more tightly
by U/Pb zircon dating with the interpreted age of the Alma Gneiss (1691±12 Ma; Nutman
and Ehlers, 1998), Rasp Ridge Gneiss (1700-1690 Ma; Nutman and Ehlers, 1998), Hores
Gneiss (1690±5 Ma; Page and Laing, 1992; 1686±3 Ma, Page et al., 2000) and the Paragon
Group (1676±10 Ma; Ehlers et al., 1996). 1690 Ma has become the accepted (Parr and
Plimer, 1993; Stevens and Burton, 1998; Cartwright, 1999; Vassallo and Vernon, 2000)
broad depositional age for Willyama Supergroup.
7
Chapter Two – Broken Hill Geology
Table 2.1.2a: Summary of the post-depositional tectonic history of the Broken Hill Block.
Event Metamorphic
Conditions
Evidenced
Deformation Date
D1/M1/F1
Olarian Orogeny
Peak prograde event
T= 750-800oC
P= 5-6 kb
(Phillips, 1980; Stevens, 1986).
Prograde mineral growth
defining S1 foliation and
regional F1 E-W-trending
nappe-like folds.
1600 Ma (Page and Laing,
1992) or 1690-1680 Ma
(Nutman and Ehlers, 1998).
D2/M2/F2
Olarian Orogeny Peak prograde event
T= 750-800oC
P= 5-6 kb (Phillips, 1980;
Stevens, 1986).
Prograde mineral growth
defining S2 foliation and the
regional F2 steeply dipping
NE-SW-trending folds.
1600-1590 Ma (Page and
Laing, 1992), 1596+3 Ma
(Page et al., 2000) or 1660-
1640 Ma (Nutman and Ehlers,
1998).
D3/M3/F3 (F4)
Olarian Orogeny
Retrograde event
T= 550-600 oC
P= 5-5.5 kb
(Stevens, 1986) or
Peak prograde event
(Nutman and Ehlers, 1998).
Retrograde mineral growth
defining S3 foliation and
shear zone propagation
accompanied by N-S and NE-
SW trending folds.
1600-1570 Ma
(Page and Laing, 1992;
Nutman and Ehlers, 1998).
D4
Grenville Orogeny
Retrograde event
T=300-400oC
(Stevens, 1999).
Retrograde shear zone
reactivation with regional
uplift.
1250-1100 Ma
(Stevens, 1986).
D5
Delamerian Orogeny Retrograde event
T = 350oC
P = 2 kb
(Pidgeon, 1967; Harrison and
McDougall, 1981).
Emplacement of ultrabasic
dykes and plugs followed by
retrograde shear zone
reactivation and the
emplacement of further
pegmatites.
561+7 Ma
520+4 Ma to 458 Ma
(Harrison and McDougall,
1981).
Five main tectonic events (Table 2.2) have been recognised in literature, however
the geochronology of these has been strongly debated. Initial studies suggested peak
metamorphism at 1660+10 Ma, possibly as two thermal events, based on Rb-Sr and zircon
dating (Pidgeon, 1967; Gulson, 1984). Recent studies have suggested two refined, yet
opposing geochronologies. Page and Laing (1992) suggest two high-grade thermal events
occurring in close temporal association during the Olarian Orogeny at approximately 1600
Ma, followed by a single retrograde event dated at 1600-1570 Ma. This geochronology is
commensurate with previous structural studies of the Broken Hill Block (Laing et al.,
1978). Alternatively, Nutman and Ehlers (1998) suggest three peak high-grade thermal
events, occurring during the Olarian Orogeny at 1690-1680 Ma, 1660-1640 Ma and 1600-
1570 Ma. Both geochronologies based on SHRIMP U-Pb dating of zircons, have gained
partial support and remain a source of contention (Stevens, 1999; Nutman and Ehlers,
1999; Page et al., 2000). Peak prograde metamorphic conditions were of high thermal
grade at 750-800oC, and low to moderate pressure of between 5-6 kb, occurring at an
8
Chapter Two – Broken Hill Geology
estimated depth of 16-20 km (Stevens, 1986). This resulting in the granulite faces
metamorphism of lower stratigraphic sequences, amphibolite facies metamorphism of the
middle sequences and greenshist facies metamorphism of the upper sequences. The
metamorphic grade of the stratigraphic units reflects this, increasing from the NW to the
SE (Figure 2.2) in the Broken Hill Block (Phillips, 1980).
Figure 2.3: Pressure verses temperature
diagram for the metamorphic evolution of
the Broken Hill Block, showing the prograde
evolution path as a result of increased
pressure and temperature during M1 and
M2, and the retrograde evolution path as a
result of the decrease in temperature that
occurred during M3 (from Hobbs et al.,
1984).
Figure 2.2: Broken Hill Block showing the
decrease in metamorphic grade from the
north-west to the south-east on the basis of
the mineral assemblage (from Slack et al.,
1989).
Retrogression started shortly after peak metamorphism with water released from
anatectic melts during cooling (Laing et al., 1978) being taken up by the crystallisation of
kyanite-staurolite and chloritoid assemblages (Figure 2.3)(Stevens, 1986). Muscovite-
bearing pegmatites and granites were emplaced in the region about 1420+20 Ma (Pidgeon,
1967), followed by a thermal pulse of approximately 300-400oC between 1250-1100 Ma
during the Grenville Orogeny causing reactivation of retrograde shear zones and regional
uplift (Stevens, 1986). Following this was a prolonged period of erosion and some
accompanying sedimentary deposition between 1100 Ma and 600 Ma. Dolerite and
pyroxenite dykes intruded close to 830 Ma (Stevens, 1986). The emplacement of ultrabasic
9
Chapter Two – Broken Hill Geology
dykes and plugs around 561+7 Ma (Harrison and McDougall, 1981) preceded a low-grade
retrogression event occurring during the Delamerian Orogeny at 520+4 Ma (Pidgeon,
1967; Harrison and McDougall, 1981) causing retrograde shear zones to reactivate along
with the emplacement of further pegmatites. Minor fault movement in shear zones, further
erosion, uplift and regolith weathering has continued in the region to the present day.
2.1.3 Structural History
The Broken Hill Block is structurally complex and as a result, the deformation history is
yet to be conclusively determined. Most studies have documented three or four major
folding events and one of shear zone formation (Table 2.2) (Laing et al., 1978; Hobbs et
al., 1984; Laing, 1996) although further folding events and shearing events have been
suggested. The first folding event, F1, was coeval with the first regional peak prograde
metamorphic event of the Olarian Orogeny, M1, and involved very large scale (>10 km),
reclined to recumbent nappe-like isoclinal east-west trending folds (Laing et al., 1978;
Hobbs et al., 1984). S1 is defined in some amphibolite to granulite facies assemblages by
prograde sillimanite and is commonly parallel with bedding (Laing et al., 1978). Bedding
and younging directions have been recognised in some metasediment outcrops. The second
folding event, F2, occurred during the second regional peak prograde metamorphic event of
the Olarian Orogeny, M2 and involved medium scale 1-10 km steeply-dipping, NW-SE-
trending folds. It is recognised by a S2 schistosity commonly defined by sillimanite and is
visible in an array of Willyama Supergroup assemblages.
During the initial stages of the retrograde metamorphic event M3, the F3 folding
event occurred, creating small-scale N-S-trending folds, almost coaxial with F2. A fourth
folding event, F4, suggested by Hobbs et al. (1984) present in the western and north-
western areas of the Broken Hill Block, produced small-scale NE-SW-trending folds, and
occurred shortly after F3, resulting in dome and basin interference patterns with the F3
structures. D5 occurred during the final stages of the M3 retrograde metamorphic event
involving the formation of numerous steeply dipping retrograde shear zones within the
Broken Hill Block primarily in NE-SW and NW-SE orientations. Reactivation of these D5
retrograde shear zones and the creation of further retrograde shear zones occurred during
the Grenville Orogeny, and the Delamerian Orogeny. All shear zones are of lower
amphibolite to greenschist metamorphic grade and comprise fine-grained micaceous
schists (Hobbs et al., 1984).
10
Chapter Two – Broken Hill Geology
2.2 Main Lode Orebody Geology 2.2.1 Stratigraphy
There are three stratigraphic suites of the Willyama Supergroup present within the main
lode mine leases (Figure 2.4). These include Suite 3, the Thackaringa Group, Suite 4, the
Broken Hill Group and Suite 5, the Sundown Group (Stevens et al., 1980). Further
lithostratigraphic study by Haydon and McConachy (1987) within the mine leases led to
the subdivision of specific suites into numerically ascending units. The Hores Gneiss (Unit
4.7) is the primary ore-bearing unit in the mine leases. It contains a number of “Potosi
Gneiss” lenses as well as pelitic and psammopelitic metasediments and associated lode
rocks (Haydon and McConachy, 1987). Retrograde shear zones, in particular the Globe
Vauxhall Shear, Western Shear and the Main Eastern Shear zones have caused offset of
stratigraphic units (Laing et al, 1978; Haydon and McConachy, 1987).
Figure 2.4: Mine lease cross-section
showing the stratigraphic suites,
Hores Gneiss and location of the main
lode orebody. Also shown are the
Broken Hill Antiform, Hanging Wall
Synform and Globe Vauxhall Shear
(from Laing et al., 1978).
2.2.2 Structure
The structure of the main lode mine leases has been interpreted by a number of authors
(Andrews, 1922; Gustafson et al., 1950; Ransom, 1968; Hodgson, 1975; Laing et al, 1978;
11
Chapter Two – Broken Hill Geology
Haydon and McConachy, 1987; Rothery, 2001). It is currently accepted (Plimer, 1984;
Haydon and McConachy, 1987; Stevens, 1995) that the main lode orebody lies on a
downward-facing limb of an F1 fold from stratigraphic vergence and younging data (Laing
et al., 1978). The northern extent of the orebody plunges to the north at approximately 40o,
while the southern extent plunges south at approximately 20-25o (Figure 2.5). The main
structures observed in the central mine leases are F2 in age.
Figure 2.5: Longitudinal profile of the Broken Hill orebody showing the CML7 lease boundary,
Kintore pit and generalised ore lode positions. The zinc lodes are concentrated at the southern
extent of the orebody (from Consolidated Broken Hill Ltd.).
2.2.3 Mineralisation
The main lode mineralisation is stratabound within lenses of the quartzofeldspathic garnet-
rich “Potosi Gneiss”. There are eight separate lodes of ore (Haydon and McConachy,
1987) within the central mine leases that form an en echelon stack (Figure 2.6). The
stratigraphic order of the ore lodes (taking into account that the current stratigraphy has
been inverted) is the C Lode, B Lode, Upper A Lode, Lower A Lode, Upper 1 Lens, Lower
1 Lens, 2 Lens and 3 Lens. Each lode has its own characteristic gangue mineralogy and
base-metal content. The C Lode, B Lode, A Lode (Upper and Lower), and 1 Lens (Upper
and Lower) are known as zinc lodes (Matthias, 1974) due to the relatively high Zn:Pb ratio
compared to 2 Lens and 3 Lens.
12
Chapter Two – Broken Hill Geology
Figure 2.6: Section 30 cross-section
looking south, showing the folded
nature of the eight ore lenses and the
attenuation of the 2 Lens and 3 Lens
caused by the Globe Vauxhall Shear
(from Haydon and McConachy,
1987).
The B and A Lodes are only developed in the CML7 and southern mine leases
while 1 Lens although thickest in the southern mine leases, continues to the northern leases
where it is only a few centimetres thick. B Lode, A Lode and 1 Lens are typically
contained within envelopes of pink garnet quartzite. Close to sulphides, the abundance of
pink garnet quartzite decreases as it is cross-cut by blue lode quartz. Juxtaposed to sulphide
rocks, the percentage of blue quartz increases in association with green gahnite crystals.
The main ore lodes occur as massive sulphides with minor quartz and garnet. Late stage
coarse galena-chalcopyrite-pyrrhotite bearing quartz veins transgress the main ore and
surrounding lode horizon rocks.
2.3 Ore Deposit Genesis Models The origin of the sulphide lodes at Broken Hill has been a source of conjecture for a long
time and there are numerous postulated genetic models. Even after more than 400
published papers on the Broken Hill orebody, no consensus has yet been reached. The
13
Chapter Two – Broken Hill Geology
earliest ideas were based on the epigenetic deposition of the orebodies (Andrews, 1922;
Gustafson et al., 1950) via the preferential replacement of sedimentary layers. In contrast,
a syngenetic model was proposed (King and Thomson, 1953) and has been refined by
numerous authors (Stanton, 1976; Laing et al., 1978; Willis et al., 1983; Plimer, 1984;
Stevens et al., 1988; Parr and Plimer, 1993). In this model the orebody is coeval with the
enclosing rocks. It is suggested that the orebody is of submarine exhalative origin within
an intracontinental rift setting. Submarine hydrothermal activity is either driven by an
intrusion or by thinning of the crust through rifting (Figure 2.7). This model has been
supported by recent literature (Willis et al., 1988; Parr and Plimer, 1993; Laing, 1996;
Large et al., 1996; Walters, 1998).
Figure 2.7: Proposed model for the genesis of the Broken Hill orebody through syngenetic submarine
exhalative mechanisms (after Parr and Plimer, 1993).
Wright et al. (1987) suggested that mineralisation was generated by compactive
expulsion of metal-bearing basin brines during sedimentation. They suggest the orebody is
formed in a large scale sedimentary basin, with Pb-Zn-rich brines travelling along
preferential pathways such as psammitic sandstones to a point where they were capped by
overlying impermeable pelitic sediments, forming the orebody during diagenesis of the
compacting sediments (Wright et al., 1987). This model is partially supported by Haydon
and McConachy (1987) and Cook and Ashley (1992) while disputed by Plimer and
Lottermoser (1988) and Willis et al. (1988). Further comment was made by Wright et al.
(1988a, b). Recently a revised epigenetic model has been proposed (Ehlers et al., 1996)
14
Chapter Two – Broken Hill Geology
with the mineralisation suggested to have occurred coeval with regional metamorphism
after the deposition of the enclosing rocks. This model was based on the result of
contentious U/Pb dating of zircons from the Broken Hill orebody, which were later
disputed by Carr and Sun (1996).
15
Chapter One - Introduction
Chapter One – Introduction 1.1 Background The Broken Hill Pb-Zn-Ag ore deposit is situated within an inlier of deformed and
metamorphosed Palaeoproterozoic rocks known as the Broken Hill Block (Figure 1.1)
within the Curnamona Craton, in western New South Wales and South Australia (Willis et
al., 1983). The Curnamona Craton covers approximately 40,000 km2 and consists of the
Broken Hill, Olary and Eurowie Blocks and the Mt Painter and Mt Babbage Inliers (Teale
and Flint, 1993).
Figure 1.1: Location of the
Broken Hill Block within
the Curnamona Craton, in
western New South Wales
and South Australia. The
Mt Painter and Mt Babbage
Inliers (not shown) are
located approximately 200
km north-west of the Olary
Block (after Cook and
Ashley, 1992).
1
Chapter One - Introduction
The Broken Hill Block contains metasedimentary and metavolcanic sequences of
pelitic, psammitic, quartzofeldspathic and mafic composition comprising the Willyama
Supergroup (Willis et al., 1983). The main lode orebody is estimated to have contained in
excess of 300 million tonnes of sulphide ore prior to mining with grades exceeding 15%
combined lead and zinc (Haydon and McConachy, 1987), with associated silver and gold.
It is considered a super giant orebody (Figure 1.2) by world standards (Large et al., 2002).
Figure 1.2: Tonnes of metal
verses Zn + Pb grade for giant
and supergiant stratiform
sediment hosted Zn-Pb-Ag
ore deposits comprised of
sedimentary exhalative-type
(SEDEX), Mississippi Valley-
type (MVT), Broken Hill-type
(BHT) and Irish style deposits
(after Large et al., 2002).
Recent discoveries of the Burke Street, Crystal Lane, Tin Street, Potosi, Flying
Doctor and Silver Peak mineralisations (Haydon and McConachy, 1987; Stevens and
Burton, 1998) have renewed waning scientific and exploration interest for base metals
within the Broken Hill Block. Consolidated Broken Hill Ltd. (CBH) is the current lease
holder of Consolidated Mining Lease 7 (CML7) which covers the central section of the
Broken Hill main lode, previously known as the Broken Hill South Mine.
1.2 Research Aims The primary objective of this honours research report is to provide a comprehensive
mineralogical and geochemical analysis of the B Lode, A Lode and 1 Lens zinc lodes on
CML7, and document the effects of regional metamorphism and deformation on the
sulphide rocks. This may allow constraints to be placed upon models for the genesis of the
2
Chapter One - Introduction
Broken Hill orebody. To achieve the primary objectives, a series of aims have been
determined. These are:
o To document the mineralogy and geochemistry of the B Lode, A Lodes and 1 Lens
from core drilled on the CML7 mine lease,
o To document the mineralogy and geochemistry of an ore lode exposed in the base of
the Kintore pit on the CML7 mine lease,
o To investigate textural relationships of sulphide minerals which may indicate
movement of sulphides along the limbs of fold structures during deformation,
o To observe the distribution and phases that Ag occurs within, which may give an
indication of Ag movement during the long history of metamorphism, and
o To look for evidence showing the sulphide rocks have undergone multiple high-grade
metamorphic events and any other evidence that can place constraints on the proposed
models for the genesis of the orebody.
1.3 Research Methods This honours research report presents observations and the analysis of samples collected
during time spent in the field at Broken Hill between Monday 8th of April and Monday 29th
of April 2002. Fieldwork involved logging and sampling three diamond drill cores totalling
746 metres, and the logging and bulk sampling along three traverses across an exposed ore
lode in the Kintore pit, termed the Kintore Lode in this report. From the samples collected,
the following analyses have been completed:
o Major, trace, rare earth and halide elements have been analysed across B Lode, A
Lode, 1 Lens and Kintore Lode samples at AMDEL Ltd. using ICP-OES, ICP-MS,
gravimetric and titration techniques.
o Polished thin section microscopy of sections at The University of Melbourne under
reflected and transmitted light.
o Electron microprobe analysis of sulphide and gangue minerals from B Lode, A Lode, 1
Lens and Kintore Lode samples at The University of Melbourne.
o Stable isotope analyses of O and C from carbonate filled microfractures within B Lode
at Monash University.
3
Chapter One - Introduction
1.4 Previous Studies
The Broken Hill Pb-Zn-Ag orebody is the world’s largest base metal orebody. Key studies
include Andrews (1912), Gustafson et al. (1950), Laing et al. (1978); Stevens et al. (1980,
1988), Willis et al. (1983), Haydon and McConachy (1987) and Parr and Plimer (1993).
These studies have focused on the provenance of the orebody in a regional, tectonic or
metallogenic context.
Other studies have focussed on geochemistry, either at a regional scale,
investigating the metavolcanic or metasedimentary units of the Broken Hill Block (Main et
al., 1983; Slack and Stevens, 1994) or at a local scale, primarily investigating the
individual lead-rich ore lodes within various orebodies of the Broken Hill Block (Both,
1973; Johnson and Klingner, 1975; Spry and Wonder, 1989). Previous studies that have
investigated the geochemistry of the zinc-rich B Lode, A Lode and 1 Lens in detail include
Stanton (1972) and Matthias (1974). However, neither of these studies analysed samples
from within the CML7 lease area. Two studies (Plimer, 1980; Both and Stumpfl, 1987)
have investigated the distribution and mobilisation of silver within the Broken Hill
orebody. There is one published report by mine geologists at the time, briefly documenting
the geology of the Broken Hill South Mine (van der Heyden and Edgecombe, 1990) and
one report documenting the structure of the orebody, with reference to the Kintore pit
(Rothery, 2001).
CML7 is completely devoid of detailed geochemical and mineralogical studies of
the zinc lodes. This is due to the fact that it was only recently discovered that the zinc lodes
continue onto CML7 from the Pasminco South Mines area. Underground mining on CML7
ceased over 25 years ago. Plans by the current operators to recommence mining operations
shortly have been a driving force behind recent studies on CML7. These include detailed
geochemical analysis of the C Lode and 2 Lens by Sproal (2001) and the Western
Mineralisation and dolerite dykes by Kitchen (2001).
Despite the volume of studies of the Broken Hill orebody and surrounding geology,
there are numerous conflicting views on many issues, from identification of pre-
metamorphic lithologies and origin of the orebodies, to partial melting and subsequent
mobilisation of the ore lodes. As a result, the paradigm for Broken Hill-type deposits,
based on the knowledge of the Broken Hill orebody, is continually evolving.
4
Chapter Two – Broken Hill Geology
Chapter Two - Broken Hill Geology
2.1 Regional Geology 2.1.1 Stratigraphy
The stratigraphy of the Broken Hill Block (Figure 2.1) described by Stevens et al. (1980,
1988) and by Willis et al. (1983) is still currently generally supported in the literature
including Parr and Plimer (1993), Laing (1996), Stevens and Burton (1998) and Walters
(1998). Due to an intense, prolonged metamorphic and deformation history at Broken Hill,
the recognition of lithological protoliths is exceedingly difficult. As a consequence, there
have been some studies that have disputed parts of the interpreted stratigraphy (e.g.
Haydon and McConachy, 1987; Wright et al., 1987; Vassallo and Vernon, 2000). In light
of new studies, the interpreted stratigraphy of the Willyama Supergroup in proximity of the
orebodies needs constant re-evaluation.
Figure 2.1: Stratigraphy of
the Willyama Supergroup
described by Willis et al.
(1983), also highlighting the
depositional trends and
occurrence of mineralisation
and exhalative sediments
(after Parr and Plimer, 1993).
5
Chapter Two – Broken Hill Geology
Regional mapping by the New South Wales Geological Survey was instrumental in
the re-classification of the Willyama Supergroup (Willis et al., 1983) into smaller “rock
type associations” called suites (Stevens et al., 1980). The lowest suite of the Willyama
Supergroup identified is the Clevedale Migmatite, followed by the Thorndale Composite
Gneiss, although recently classified units, the Redan Gneiss, Ednas Gneiss and Mulculca
Formation (Stevens et al., 1988) in the south-east of the Broken Hill Block are thought to
occur stratigraphically beneath or equivalent to the Clevedale Migmatite and Thorndale
Composite Gneiss. Overlying these is the Thackaringa Group, which is followed by the
Broken Hill Group, the Sundown Group and the uppermost sequence, the Paragon Group
(Table 2.1). The principal trend is from the quartzo-feldspathic rich lithostratigraphic
sequences of the Thackaringa Group, through the mineralised and exhalative
lithstratigraphic sequences of the Broken Hill Group, to the metasediment-rich sequences
of the Sundown and Paragon Groups (Parr and Plimer, 1993).
Table 2.1.1a: Lithostratigraphic units of the Willyama Supergroup and their interpreted protoliths.
Stratigraphic
Name
Suite
Unit Lithology Interpreted Protolith
Clevedale Migmatite > 500m
1
Poorly bedded feldspathic gneiss, migmatite
metasediment and minor amphibolite (Stevens
et al., 1980).
Detrital sediments containing volcanic detritus
and ash fall tuffs (Stevens et al., 1988).
Thorndale Composite Gneiss 1000m
2
Thinly to poorly bedded metasedimentary and
quartzo-feldspathic composite gneiss and
amphibolite (Stevens et al., 1980)
Fluvial-deltaic feldspathic sand deposition
(Stevens et al., 1988).
Thackaringa Group 1500m
3
Lady Brassey 3.1 Na-plagioclase-quartz rocks (Stevens et al.,
1988).
Na volcanics or air fall tuffs altered by alkaline
lake or seawater (Stevens et al., 1988).
Alma Gneiss 3.2 Coarse grained granitic rock with K feldspar
megacrysts (Willis et al., 1983)
Rhyodacitic lava-flows or ash-flow tuffs (Stevens
et al., 1988) or granitoid intrusion (Vassallo and
Vernon, 2000).
Alders Tank Formation
3.3-
3.4
Metasedimentary and quartzo-feldspathic
composite gneiss (Stevens et al., 1988).
Deep-water turbidite fans or deltaic and
lacustrine deposits (Stevens et al., 1988).
Cues Formation 3.5
Metasedimentary composite gneiss and
metasediments with leucocratic, garnet-biotite
and basic gneisses (Stevens et al., 1988).
Deep-water turbidite fans or deltaic lacustrine
deposits (Stevens et al., 1988).
Himalaya Formation
3.6-
3.9
Na-plagioclase-quartz rocks (Stevens et al.,
1988).
Na volcanics or air fall tuffs altered by alkaline
lake or seawater (Stevens et al., 1988).
Rasp Ridge 3.10 Quartzo-feldspathic gneiss (Stevens et al.,
1980).
Rhyodacitic lava-flows or ash-flow tuffs (Stevens
et al., 1988) or granitoid intrusion (Vassallo and
Vernon, 2000).
6
Chapter Two – Broken Hill Geology
Broken Hill Group 500m
4
Allendale Metasediments
4.1-
4.3
Feldspar-rich and quartz-rich psammitic
metasediments (Stevens et al., 1988).
Deep-water turbidite fans or deltaic and
lacustrine deposits (Stevens et al., 1988).
Parnell Formation
4.4
Amphibolite/basic granulite, garnetiferous
quartzo-feldspathic gneiss and quartz-
garnet/quartz-gahnite rock (Stevens et al.,
1988).
Bimodal rhyodacite-tholeiitic basalt volcanism
with associated exhalites (Stevens et al., 1988) or
marine transgression sequence with storm surge
layers (Wright et al., 1987).
Freyers Metasediment
4.5-
4.6
Well-bedded metasediments of pelitic to
psammitic composition. Offshore marine turbidite or shallow storm/wave base sequence (Stevens et al., 1988).
Hores Gneiss 4.7
Garnetiferous quartzo-feldspathic gneiss and
intercalated metasediments (Stevens et al.,
1988).
Felsic volcanic or volcaniclastic rock (Willis et
al., 1983; Stevens et al., 1988) or arkose
sandstone (Haydon and McConachy, 1987;
Wright et al., 1987).
Silver King Formation
4.8 Massive amphibolites intercalated with
metasediments (Stevens et al., 1988).
Mass flow acid volcanics with intercalated shelf
muds and silts (Stevens et al., 1988).
Sundown Group 1000m
5
Thin bedded pelitic to psammopelitic
metasediments and minor calc-silicates
(Stevens et al., 1980).
Diagenetic carbonate and turbiditic sedimentation
in a marine environment (Stevens et al., 1988) or
sag phase rift-fill sedimentation (Parr and Plimer,
1993).
Paragon Group >2200m
6-8
Well bedded to laminated fine-grained pelitic
schists and psammitic metasediments with
abundant graphitic metasediment (Stevens et
al., 1980).
Deep marine turbidite sequence or shallow
storm/wave base shelf sequence (Stevens et al.,
1988).
2.1.2 Age and Metamorphic History
The Broken Hill Block has undergone a long and intense metamorphic history (Table 2.2).
As a result, precise dating of the Willyama Supergroup stratigraphic units is problematic,
linked to the polymetamorphic history at Broken Hill, with resetting of zircons common
during metamorphism.
Early studies of the Broken Hill Block broadly confined the age of deposition to
1820±100 Ma (Pidgeon, 1967) after the separation of the crust from the mantle at 2100-
2300 Ma (McCulloch and Hensel, 1984). This has recently been constrained more tightly
by U/Pb zircon dating with the interpreted age of the Alma Gneiss (1691±12 Ma; Nutman
and Ehlers, 1998), Rasp Ridge Gneiss (1700-1690 Ma; Nutman and Ehlers, 1998), Hores
Gneiss (1690±5 Ma; Page and Laing, 1992; 1686±3 Ma, Page et al., 2000) and the Paragon
Group (1676±10 Ma; Ehlers et al., 1996). 1690 Ma has become the accepted (Parr and
Plimer, 1993; Stevens and Burton, 1998; Cartwright, 1999; Vassallo and Vernon, 2000)
broad depositional age for Willyama Supergroup.
7
Chapter Two – Broken Hill Geology
Table 2.1.2a: Summary of the post-depositional tectonic history of the Broken Hill Block.
Event Metamorphic
Conditions
Evidenced
Deformation Date
D1/M1/F1
Olarian Orogeny
Peak prograde event
T= 750-800oC
P= 5-6 kb
(Phillips, 1980; Stevens, 1986).
Prograde mineral growth
defining S1 foliation and
regional F1 E-W-trending
nappe-like folds.
1600 Ma (Page and Laing,
1992) or 1690-1680 Ma
(Nutman and Ehlers, 1998).
D2/M2/F2
Olarian Orogeny Peak prograde event
T= 750-800oC
P= 5-6 kb (Phillips, 1980;
Stevens, 1986).
Prograde mineral growth
defining S2 foliation and the
regional F2 steeply dipping
NE-SW-trending folds.
1600-1590 Ma (Page and
Laing, 1992), 1596+3 Ma
(Page et al., 2000) or 1660-
1640 Ma (Nutman and Ehlers,
1998).
D3/M3/F3 (F4)
Olarian Orogeny
Retrograde event
T= 550-600 oC
P= 5-5.5 kb
(Stevens, 1986) or
Peak prograde event
(Nutman and Ehlers, 1998).
Retrograde mineral growth
defining S3 foliation and
shear zone propagation
accompanied by N-S and NE-
SW trending folds.
1600-1570 Ma
(Page and Laing, 1992;
Nutman and Ehlers, 1998).
D4
Grenville Orogeny
Retrograde event
T=300-400oC
(Stevens, 1999).
Retrograde shear zone
reactivation with regional
uplift.
1250-1100 Ma
(Stevens, 1986).
D5
Delamerian Orogeny Retrograde event
T = 350oC
P = 2 kb
(Pidgeon, 1967; Harrison and
McDougall, 1981).
Emplacement of ultrabasic
dykes and plugs followed by
retrograde shear zone
reactivation and the
emplacement of further
pegmatites.
561+7 Ma
520+4 Ma to 458 Ma
(Harrison and McDougall,
1981).
Five main tectonic events (Table 2.2) have been recognised in literature, however
the geochronology of these has been strongly debated. Initial studies suggested peak
metamorphism at 1660+10 Ma, possibly as two thermal events, based on Rb-Sr and zircon
dating (Pidgeon, 1967; Gulson, 1984). Recent studies have suggested two refined, yet
opposing geochronologies. Page and Laing (1992) suggest two high-grade thermal events
occurring in close temporal association during the Olarian Orogeny at approximately 1600
Ma, followed by a single retrograde event dated at 1600-1570 Ma. This geochronology is
commensurate with previous structural studies of the Broken Hill Block (Laing et al.,
1978). Alternatively, Nutman and Ehlers (1998) suggest three peak high-grade thermal
events, occurring during the Olarian Orogeny at 1690-1680 Ma, 1660-1640 Ma and 1600-
1570 Ma. Both geochronologies based on SHRIMP U-Pb dating of zircons, have gained
partial support and remain a source of contention (Stevens, 1999; Nutman and Ehlers,
1999; Page et al., 2000). Peak prograde metamorphic conditions were of high thermal
grade at 750-800oC, and low to moderate pressure of between 5-6 kb, occurring at an
8
Chapter Two – Broken Hill Geology
estimated depth of 16-20 km (Stevens, 1986). This resulting in the granulite faces
metamorphism of lower stratigraphic sequences, amphibolite facies metamorphism of the
middle sequences and greenshist facies metamorphism of the upper sequences. The
metamorphic grade of the stratigraphic units reflects this, increasing from the NW to the
SE (Figure 2.2) in the Broken Hill Block (Phillips, 1980).
Figure 2.3: Pressure verses temperature
diagram for the metamorphic evolution of
the Broken Hill Block, showing the prograde
evolution path as a result of increased
pressure and temperature during M1 and
M2, and the retrograde evolution path as a
result of the decrease in temperature that
occurred during M3 (from Hobbs et al.,
1984).
Figure 2.2: Broken Hill Block showing the
decrease in metamorphic grade from the
north-west to the south-east on the basis of
the mineral assemblage (from Slack et al.,
1989).
Retrogression started shortly after peak metamorphism with water released from
anatectic melts during cooling (Laing et al., 1978) being taken up by the crystallisation of
kyanite-staurolite and chloritoid assemblages (Figure 2.3)(Stevens, 1986). Muscovite-
bearing pegmatites and granites were emplaced in the region about 1420+20 Ma (Pidgeon,
1967), followed by a thermal pulse of approximately 300-400oC between 1250-1100 Ma
during the Grenville Orogeny causing reactivation of retrograde shear zones and regional
uplift (Stevens, 1986). Following this was a prolonged period of erosion and some
accompanying sedimentary deposition between 1100 Ma and 600 Ma. Dolerite and
pyroxenite dykes intruded close to 830 Ma (Stevens, 1986). The emplacement of ultrabasic
9
Chapter Two – Broken Hill Geology
dykes and plugs around 561+7 Ma (Harrison and McDougall, 1981) preceded a low-grade
retrogression event occurring during the Delamerian Orogeny at 520+4 Ma (Pidgeon,
1967; Harrison and McDougall, 1981) causing retrograde shear zones to reactivate along
with the emplacement of further pegmatites. Minor fault movement in shear zones, further
erosion, uplift and regolith weathering has continued in the region to the present day.
2.1.3 Structural History
The Broken Hill Block is structurally complex and as a result, the deformation history is
yet to be conclusively determined. Most studies have documented three or four major
folding events and one of shear zone formation (Table 2.2) (Laing et al., 1978; Hobbs et
al., 1984; Laing, 1996) although further folding events and shearing events have been
suggested. The first folding event, F1, was coeval with the first regional peak prograde
metamorphic event of the Olarian Orogeny, M1, and involved very large scale (>10 km),
reclined to recumbent nappe-like isoclinal east-west trending folds (Laing et al., 1978;
Hobbs et al., 1984). S1 is defined in some amphibolite to granulite facies assemblages by
prograde sillimanite and is commonly parallel with bedding (Laing et al., 1978). Bedding
and younging directions have been recognised in some metasediment outcrops. The second
folding event, F2, occurred during the second regional peak prograde metamorphic event of
the Olarian Orogeny, M2 and involved medium scale 1-10 km steeply-dipping, NW-SE-
trending folds. It is recognised by a S2 schistosity commonly defined by sillimanite and is
visible in an array of Willyama Supergroup assemblages.
During the initial stages of the retrograde metamorphic event M3, the F3 folding
event occurred, creating small-scale N-S-trending folds, almost coaxial with F2. A fourth
folding event, F4, suggested by Hobbs et al. (1984) present in the western and north-
western areas of the Broken Hill Block, produced small-scale NE-SW-trending folds, and
occurred shortly after F3, resulting in dome and basin interference patterns with the F3
structures. D5 occurred during the final stages of the M3 retrograde metamorphic event
involving the formation of numerous steeply dipping retrograde shear zones within the
Broken Hill Block primarily in NE-SW and NW-SE orientations. Reactivation of these D5
retrograde shear zones and the creation of further retrograde shear zones occurred during
the Grenville Orogeny, and the Delamerian Orogeny. All shear zones are of lower
amphibolite to greenschist metamorphic grade and comprise fine-grained micaceous
schists (Hobbs et al., 1984).
10
Chapter Two – Broken Hill Geology
2.2 Main Lode Orebody Geology 2.2.1 Stratigraphy
There are three stratigraphic suites of the Willyama Supergroup present within the main
lode mine leases (Figure 2.4). These include Suite 3, the Thackaringa Group, Suite 4, the
Broken Hill Group and Suite 5, the Sundown Group (Stevens et al., 1980). Further
lithostratigraphic study by Haydon and McConachy (1987) within the mine leases led to
the subdivision of specific suites into numerically ascending units. The Hores Gneiss (Unit
4.7) is the primary ore-bearing unit in the mine leases. It contains a number of “Potosi
Gneiss” lenses as well as pelitic and psammopelitic metasediments and associated lode
rocks (Haydon and McConachy, 1987). Retrograde shear zones, in particular the Globe
Vauxhall Shear, Western Shear and the Main Eastern Shear zones have caused offset of
stratigraphic units (Laing et al, 1978; Haydon and McConachy, 1987).
Figure 2.4: Mine lease cross-section
showing the stratigraphic suites,
Hores Gneiss and location of the main
lode orebody. Also shown are the
Broken Hill Antiform, Hanging Wall
Synform and Globe Vauxhall Shear
(from Laing et al., 1978).
2.2.2 Structure
The structure of the main lode mine leases has been interpreted by a number of authors
(Andrews, 1922; Gustafson et al., 1950; Ransom, 1968; Hodgson, 1975; Laing et al, 1978;
11
Chapter Two – Broken Hill Geology
Haydon and McConachy, 1987; Rothery, 2001). It is currently accepted (Plimer, 1984;
Haydon and McConachy, 1987; Stevens, 1995) that the main lode orebody lies on a
downward-facing limb of an F1 fold from stratigraphic vergence and younging data (Laing
et al., 1978). The northern extent of the orebody plunges to the north at approximately 40o,
while the southern extent plunges south at approximately 20-25o (Figure 2.5). The main
structures observed in the central mine leases are F2 in age.
Figure 2.5: Longitudinal profile of the Broken Hill orebody showing the CML7 lease boundary,
Kintore pit and generalised ore lode positions. The zinc lodes are concentrated at the southern
extent of the orebody (from Consolidated Broken Hill Ltd.).
2.2.3 Mineralisation
The main lode mineralisation is stratabound within lenses of the quartzofeldspathic garnet-
rich “Potosi Gneiss”. There are eight separate lodes of ore (Haydon and McConachy,
1987) within the central mine leases that form an en echelon stack (Figure 2.6). The
stratigraphic order of the ore lodes (taking into account that the current stratigraphy has
been inverted) is the C Lode, B Lode, Upper A Lode, Lower A Lode, Upper 1 Lens, Lower
1 Lens, 2 Lens and 3 Lens. Each lode has its own characteristic gangue mineralogy and
base-metal content. The C Lode, B Lode, A Lode (Upper and Lower), and 1 Lens (Upper
and Lower) are known as zinc lodes (Matthias, 1974) due to the relatively high Zn:Pb ratio
compared to 2 Lens and 3 Lens.
12
Chapter Two – Broken Hill Geology
Figure 2.6: Section 30 cross-section
looking south, showing the folded
nature of the eight ore lenses and the
attenuation of the 2 Lens and 3 Lens
caused by the Globe Vauxhall Shear
(from Haydon and McConachy,
1987).
The B and A Lodes are only developed in the CML7 and southern mine leases
while 1 Lens although thickest in the southern mine leases, continues to the northern leases
where it is only a few centimetres thick. B Lode, A Lode and 1 Lens are typically
contained within envelopes of pink garnet quartzite. Close to sulphides, the abundance of
pink garnet quartzite decreases as it is cross-cut by blue lode quartz. Juxtaposed to sulphide
rocks, the percentage of blue quartz increases in association with green gahnite crystals.
The main ore lodes occur as massive sulphides with minor quartz and garnet. Late stage
coarse galena-chalcopyrite-pyrrhotite bearing quartz veins transgress the main ore and
surrounding lode horizon rocks.
2.3 Ore Deposit Genesis Models The origin of the sulphide lodes at Broken Hill has been a source of conjecture for a long
time and there are numerous postulated genetic models. Even after more than 400
published papers on the Broken Hill orebody, no consensus has yet been reached. The
13
Chapter Two – Broken Hill Geology
earliest ideas were based on the epigenetic deposition of the orebodies (Andrews, 1922;
Gustafson et al., 1950) via the preferential replacement of sedimentary layers. In contrast,
a syngenetic model was proposed (King and Thomson, 1953) and has been refined by
numerous authors (Stanton, 1976; Laing et al., 1978; Willis et al., 1983; Plimer, 1984;
Stevens et al., 1988; Parr and Plimer, 1993). In this model the orebody is coeval with the
enclosing rocks. It is suggested that the orebody is of submarine exhalative origin within
an intracontinental rift setting. Submarine hydrothermal activity is either driven by an
intrusion or by thinning of the crust through rifting (Figure 2.7). This model has been
supported by recent literature (Willis et al., 1988; Parr and Plimer, 1993; Laing, 1996;
Large et al., 1996; Walters, 1998).
Figure 2.7: Proposed model for the genesis of the Broken Hill orebody through syngenetic submarine
exhalative mechanisms (after Parr and Plimer, 1993).
Wright et al. (1987) suggested that mineralisation was generated by compactive
expulsion of metal-bearing basin brines during sedimentation. They suggest the orebody is
formed in a large scale sedimentary basin, with Pb-Zn-rich brines travelling along
preferential pathways such as psammitic sandstones to a point where they were capped by
overlying impermeable pelitic sediments, forming the orebody during diagenesis of the
compacting sediments (Wright et al., 1987). This model is partially supported by Haydon
and McConachy (1987) and Cook and Ashley (1992) while disputed by Plimer and
Lottermoser (1988) and Willis et al. (1988). Further comment was made by Wright et al.
(1988a, b). Recently a revised epigenetic model has been proposed (Ehlers et al., 1996)
14
Chapter Two – Broken Hill Geology
with the mineralisation suggested to have occurred coeval with regional metamorphism
after the deposition of the enclosing rocks. This model was based on the result of
contentious U/Pb dating of zircons from the Broken Hill orebody, which were later
disputed by Carr and Sun (1996).
15
Chapter Three – CML7 Geology
Chapter Three - CML7 Geology 3.1 Geology Introduction This chapter presents the field geology of drill core and open pit rocks observed while
undertaking fieldwork in Broken Hill.
Figure 3.1: CML7 lease showing drill hole locations and Kintore pit as well as the main line of lode
and Western Mineralisation projected to surface (from Consolidated Broken Hill Ltd).
3.2 Drill Core Geology 3.2.1 Drill core introduction
Three complete diamond drill cores ZLDD5000, ZLDD5001 and ZLDD5002A, totalling
746 metres were lithologically logged. The cores were drilled from the western side of the
main lode, close to the southern extent of the CML7 boundary (Figure 3.1) in an
orientation steeply dipping towards the east in an attempt to intersect the main lode ore
lenses. Logging involved identifying and documenting the mineralogy of the core and any
visible structures, such as bedding, younging, cleavages, faults, fractures, folds and
brecciation. Once the three diamond drill cores had been logged for lithology and broad
stratigraphic features, the zinc lode intersections, B Lode, A Lode and 1 Lens were
relogged in greater detail to focus on the mineralogy and the textures of the lode horizon
16
Chapter Three – CML7 Geology
and sulphide rocks. The use of a 10x hand lens, magnet, tungsten-tipped scratching tool
and hydrochloric acid aided in the logging process.
3.2.2 Drill core lithology
The drill cores were logged using a combination of the nomenclature set out by the New
South Wales Geological Survey for the Broken Hill Block and CBH (Appendix 1).
Observations made during logging were recorded on sedimentological core logs (Figures
3.8 and 3.9 and Appendix 2).
The broad stratigraphy of each diamond drill cores was very similar. The first
lithology encountered varied between pegmatite or psammitic and pelitic metasediments.
These lithologies were all highly oxidised down to about 50 metres depth due to their close
proximity to the surface and long history of weathering. Characteristic of oxidation was the
red earthy colour of psammites, the sericitisation and kaolinisation of pegmatites and the
breakdown of micas within pelites to clays. One unusual lithology observed was a 40cm
breccia of pelite with a fine-grained matrix of dark garnet (Figure 3.2).
Figure 3.2:
Brecciated pelite
with a fine-grained
garnet matrix
(from ZLDD5001-
14.8m).
Once below the oxidation zone, the lithologies varied between intercalated pelitic,
psammopelite and psammite with numerous pegmatite intervals and ore lenses surrounded
by distinctive lode horizon rocks. The pelites exhibited a light green to brown hue on
exposed surfaces as a result of slight post-drilling chloritisation of micas, however a light
grey to light brown mottled appearance is more characteristic of fresh samples. Some
sections of pelites exhibited a spotted appearance resulting from the pseudomorphing of
andalusite by sillimanite crystals averaging 4mm in size but much larger in a number of
cases. This distinctive lithology is termed ‘spotted pelite’ (Figure 3.3). The psammopelites
17
Chapter Three – CML7 Geology
and psammites (Figure 3.4) ranged from light grey to dark grey in colour and rarely had
become red with oxidation since drilling. Graded bedding was present in a number of
sections where a minor pelite bed was contained within a large psammopelitic bed (Figure
3.4) and could be used to identify younging in the metasediments. The mineralogy of
pegmatites varied between quartz and K-feldspar, to include moderate amounts of garnet +
biotite and muscovite. The pegmatites commonly occurred crosscutting S0 and S1, rarely
folding ptygmatically (Figure 3.5) in a S2 or even S3 orientation, while in other sections,
follow the S0/S1 orientation. Minor pure white quartz veins are rare. Sulphides are
commonly associated with blue lode quartz and enclosed within fine-grained pink garnet-
rich psammite known as ‘garnet quartzite’ (Figure 3.6).
Figure 3.3: Spotted
pelite in HQ core
(from ZLDD5001-
29.1m).
Figure 3.4: Reverse
bedding in pelitic
to psammopelitic
metasediments in
NQ core (from
ZLDD5001-178m).
18
Chapter Three – CML7 Geology
Figure 3.5: Ptygmatic
folding of pegmatite
in HQ core (from
ZLDD5000-200m).
Figure 3.6: Garnet
quartzite associated
with blue lode quartz
veins in HQ core
(from ZLDD5000-
163.2m).
From the logs of the three drill cores, the abundance for each main lithological type
was quantified down to an interbedded scale of 10cm (Figure 3.7). The lithologies
comprise of psammopelitic metasediment (28%), pelitic metasediments (19%), psammitic
metasediments (17%), pegmatite (13%), lode horizon (17%) and massive sulphides (4%).
Core loss accounted for 1% of the total drill core length.
Sedimentology of Drill Cores
17
28
19
1317
41
0
5
10
15
20
25
30
35
Psammite
Psammop
elite
Pelite
Pegmati
te
Lode
Hori
zon R
ocks
Massiv
e Sulp
hides
Core Lo
ss
Lithology
Abun
danc
e %
ZLDD5000
ZLDD5001
ZLDD5002A
Drill Core Average(value shown)
Figure 3.7:
Abundance of the
broadly defined
lithological types
observed in the drill
cores.
19
Chapter Three – CML7 Geology
3.2.3 B Lode Geology
The best intersection of B Lode was between 133-140m in ZLDD5001 (Figure 3.8). C
Lode was intersected from 81-84m and 89-92m prior to the B Lode intersection,
supporting the inverted nature of the Broken Hill orebody.
Prior to garnet quartzite at 127m, there was a progression from pelitic
metasediments, through psammopelitic metasediments to psammitic metasediments. B
Lode is surrounded by garnet quartzite, which is a fine-grained <2mm primarily anhedral
pink garnet “sandstone”. Minor 1cm veins of blue lode quartz and pyrrhotite>chalcopyrite
veins occur along S0/S1. Towards massive sulphides, the modal abundance of blue lode
quartz veins in the garnet quartzite increases and sulphides begin to occur disseminated
within the garnet quartzite groundmass. The progression into massive sulphides is marked
by the loss of garnet quartzite, a decrease in the blue lode quartz and an increase in
disseminated sulphides to such a degree that the rock is predominately massive sulphides,
of approximately 50% modal abundance. In B Lode, sphalerite is the most abundant
sulphide (50%), followed by galena (35%), pyrrhotite (10%) and chalcopyrite (5%). The
sulphide grains are coarse and angular, from euhedral to anhedral, increasing in grain size
with depth. Garnet quartzite occurring again at 139m is accompanied with minor
disseminated sulphides in blue lode quartz veins, which cease once a depth of 140m is
reached. At 140.1m, the garnet quartzite grades abruptly to psammopelite and by 141m,
into a thick unit of spotted pelite.
Table 3.2.3a: Abbreviations for mineral names in lithological logs (this chapter) and photomicrographs
(Chapter Five).
Gangue Mineral Abbreviation Sulphide Mineral Abbreviation
Quartz Qtz Sphalerite Sph
Garnet Gar Galena Ga
Gahnite Gah Pyrrhotite Po
Biotite Bio Chalcopyrite Cpy
Chlorite Chl Arsenopyrite Apy
Muscovite Mu Tetrahedrite Tet
Carbonate Carb Gudmundite Gud
Sillimanite Sill Pyrite Py
20
Chapter Three – CML7 Geology
Figure 3.8: Lithological log of B Lode from Hole ZLDD5001: 127-140m.
21
Chapter Three – CML7 Geology
Figure 3.9: Lithological log of A Lode from Hole ZLDD5001: 170-175m and of 1 Lens from
ZLDD5000: 181-185m.
22
Chapter Three – CML7 Geology
3.2.4 A Lode Geology
Down hole from the B Lode intersection, the core comprised a spotted pelite sequence,
interlayered with minor pegmatite layers including the distinctively green plumbian
orthoclase-rich “separation pegmatite” at 159-161m, followed by a transgression to
psammopelitic metasediments with minor layers of lode horizon rocks. Just prior to the
lode horizon, a number of pegmatites, some ptygmatically folded and containing garnet
porphyryblasts occur within a groundmass of psammopelitic metasediments. A Lode was
intersected in ZLDD5001 at the depth of 170-175m (Figure 3.9). Initially A Lode is
identified by the pink garnet quartzite lode horizon, with minor gahnite-rich white quartz
veins. A minor spotted pelite divides this unit from a further gahnite-rich quartz vein. This
is followed by further garnet quartzite, which contains a significant amount of blue lode
quartz and is intensely brecciated. The main A Lode mineralisation follows, consisting
primarily of disseminated sulphides within a blue lode quartz-garnet-gahnite rock. Initially
the sulphides are pyrrhotite>chalcopyrite, which further downhole changes to
sphalerite>chalcopyrite>pyrrhotite and becomes massive in form with 1cm crystals of
sphalerite and pyrrhotite within blue lode quartz. The massive sulphides then become
disseminated with pyrrhotite>chalcopyrite>sphalerite>galena, which was the commonly
observed mineralogy of vein style mineralisation. A decrease in sulphide content
corresponds with an increase in the garnet and gahnite abundance. A Lode grades into
intercalated psammitic and psammopelitic metasediments.
3.2.5 1 Lens Geology
In ZLDD5001, 1 Lens was not intersected. However, in drill hole ZLDD5000, 1 Lens was
intersected at a depth of 183-186m (Figure 3.9). Prior to the intersection of 1 Lens, the
sequence consisted of predominantly psammopelitic and psammitic metasediments. The
sequence was largely free of pegmatite leading into ore horizon, which began after a bed of
foliated spotted pelite interbedded with psammopelite. The lode horizon consisted of fine-
grained pink garnet quartzite with minor quartz-gahnite veins which downhole become
mineralised with chalcopyrite-pyrrhotite>galena-sphalerite. The main mineralisation in this
1 Lens intersection is contained within mineralised white quartz veins that contain
chalcopyrite>pyrrhotite-galena and garnet quartzite which contains galena-
pyrrhotite>chalcopyrite-sphalerite. Galena crystals are large and isolated. Downhole the
mineralisation is pyrrhotite>sphalerite-galena>chalcopyrite in association with gahnite. A
loss of sulphides occurs into a foliated gahnite-garnet quartz feldspar rock which is
23
Chapter Three – CML7 Geology
significantly retrogressed either side of a sericitised pegmatite vein at 188.1m, with high
biotite content, followed by a large 4m bed of garnet quartzite lode horizon which grades
into psammopelitic and psammitic sequences.
3.3 Kintore Lode 3.3.1 Kintore pit introduction
Three traverses were mapped across the Kintore Lode, exposed in a bench wall at the base
of the Kintore pit (Figure 3.10). This ore lode had been classified as A Lode by the
previous operators of the then South Mine leases (van der Heyden and Edgecombe, 1990)
however this classification is far from conclusive. The traverses, measuring 9.3m, 6.4m
and 2.9m were then logged using the same criteria as used for the drill core and a total of
13 bulk samples were collected along the traverses with the use of a sledge hammer and
steel wedge to complement the 6 samples already obtained from CBH. The traverses were
located at various intervals along the strike of the exposed ore lode (Figure 3.11).
Figure 3.10: Cross section of the Kintore pit at 335 north, showing extent of the pit when mining
stopped in 1991. Note that this section is at the south end of the pit and the traverses are located at
the north end of the pit (from Minerals Mining and Metallurgy Ltd.).
24
Chapter Three – CML7 Geology
A
N
B
N
Figure 3.11: A) Photograph of the north end of the Kintore pit looking north-west, with the
approximate position of the ore lodes highlighted. B) Photograph showing the position of the
Kintore Lode, the east verging F3 isoclinal fold and location of traverse one and two. Traverse
three was taken on another outcrop of lode 20m to the south-west along strike from this outcrop.
3.3.2 Kintore Lode Geology
The Kintore Lode has a number of distinct lithological layers, and from these the
dip and strike of the lode was measured. The ore lode strikes 30oNE and dips at 54o
towards 267oW into the bench wall. In the north facing section of the bench wall, an
isoclinal fold of the ore lode is visible (Figure 3.11) and the axial plane of this fold is also
approximately 30oNE with a plunge to the south of approximately 15o. The inferred
vergence of the fold is towards the east due to its ‘z’ geometry, and this correlates with the
position of the larger scale F3 structure known as the Western Antiform (Gustafson et al.,
1950). This suggests that the ore lode has undergone parasitic folding associated with the
F3 folding event.
25
Chapter Three – CML7 Geology
Figure 3.12: Complete log of traverse one across the Kintore Lode.
26
Chapter Three – CML7 Geology
Figure 3.13: Complete log of traverse two and three across the Kintore Lode.
27
Chapter Three – CML7 Geology
The ore lode (Figure 3.12 and 3.13) is bound by metasediments. On the bench wall,
below the ore lode, the metasediments comprise strongly foliated psammopelite, with
minor intercalated sillimanite or garnet-rich layers. The psammopelite is dark in
appearance due to oxidation on the exposed surfaces. Psammopelite grades into more
psammitic metasediments with only minor interbedded psammopelitic, corresponding to a
loss of sillimanite and biotite, with an increase in quartz and feldspar. A number of
pegmatites up to 30 centimetres in thickness are present interbedded within the psammitic
metasediments and have a high modal percentage of green plumbian orthoclase. The dip
and strike of the metasediment beds is variable (dipping up to 80o to W with a strike of
20oN) as a result of deformation and the influence of more competent layers such as the
pegmatite. Proceeding along the traverse up the bench wall, the interbedded nature of the
psammitic and psammopelitic metasediments changes for a purely psammitic composition,
rich in garnet and minor associated gahnite, before changing into the mineralised ore zone.
The mineralisation is initially disseminated within blue lode quartz veins before becoming
massive within quartz-garnet rock. The massive sulphide layers have a slightly varied
orientation, striking at 38oNE with a dip of 48o to W. Further plumbian orthoclase-rich
pegmatites are present within the ore lode, however they are very narrow, with a maximum
thickness of 10cm. The massive sulphides in hand specimen comprise coarse galena,
sphalerite, chalcopyrite and pyrrhotite within a quartz-garnet matrix. Oxidation of the
sulphides has occurred on the exposed surfaces and these are brown in appearance
resulting from sphalerite and pyrrhotite oxididation. A return to psammitic layers occurs
grading into psammopelitic metasediments that contain abundant lenses and veins of blue
lode quartz, garnet quartzite, gahnite-rich layers and minor plumbian orthoclase-bearing
pegmatites. Further along the traverses, the complete loss of garnet, gahnite and blue lode
quartz occurs with the return to psammitic-psammopelitic metasediments and this is
accompanied by an increase in the sillimanite and biotite content.
The logs have been superimposed onto a photograph of the Kintore Lode and
correlation between traverse one and two carried out, showing the approximate lithological
position of the Kintore Lode (Figure 3.14). From the logs of the Kintore Lode traverses,
the abundance for each main lithological type was quantified (Figure 3.15). The lithologies
comprise psammopelitic metasediment (27%), psammitic metasediment (20%), massive
sulphides (29%), lode horizon garnet-quartzite and gahnite rocks (17%), pegmatite (6%)
and pelitic metasediment (1%).
28
Chapter Three – CML7 Geology
Figure 3.14: A) Photograph of the Kintore Lode, with lithological logs of traverse one and two
transposed on. B) Interpreted geology of the bench wall containing the Kintore Lode, based on
correlation of the lithological logs of traverse one and two.
A
29
Chapter Three – CML7 Geology
B
29
Chapter Three – CML7 Geology
Sedimentology of Kintore Lode
20
27
16
17
29
05
101520253035404550
Psammite
Psammop
elite
Pelite
Pegmati
te
Lode
Hori
zon R
ocks
Massiv
e Sulp
hides
Lithology
Abu
ndan
ce %
Kintore T1
Kintore T2
Kintore T4
Open Pit Average(value shown)
Figure 3.15:
Abundance of the
broadly defined
lithological types
observed in the
Kintore Lode
traverses.
3.4 Discussion It is well documented that the Broken Hill Block has undergone multiple metamorphic and
deformation events. Evidence of this was in the metasediments preceding the zinc lodes in
drill core. The occurrence of spotted pelite (Figure 3.3), resulting from sillimanite crystals
pseudomorphing andalusite, is characteristic of high-grade metamorphism from
amphibolite to granulite facies (Phillips, 1980). The occurrence of pegmatites within the
metasediments indicates that partial melting has occurred during the geological history of
the metasediments. Pegmatites followed S0/S1, S2 or S3 foliations in drill core (Figure 3.5),
suggesting that multiple partial melting events occurred, which is consistent with the
metamorphic history of the Broken Hill Block. Graded bedding in drill core with
sillimanite defining the upper section of bedding, is a key tool in identifying younging and
fold attitudes. Using graded bedding (Figure 3.4) as a guide, a number of folds were
observed within the drill cores, and these were consistent with the structural history of the
Broken Hill Block. The dominant sillimanite foliation observed in the Kintore Lode may
have resulted from the F3 deformation event. The presence of intensely brecciated pelite
(Figure 3.2) with garnet dominant in the groundmass is suggestive of high-pressure fluid
flow, possibly during metamorphism resulting in the garnet growth.
Lode horizon rocks, namely the garnet quartzite horizon (Figure 3.6), and also
garnet-gahnite-quartz rocks are predominantly on the structural hanging wall, rather than
the structural footwall of the ore horizon. This may indicate that these lithologies form an
alteration halo that is D2 or later in age, resulting after overturning of the ore lodes,
30
Chapter Three – CML7 Geology
followed by the percolation of residual metamorphic fluids contained within the ore lodes
dominantly upwards into the surrounding metasediment rocks. Alternatively, if such rocks
formed pre M1/D1, they may represent a pre-metamorphic alteration assemblage (Plimer,
1979). All mineralisation is contained within lode horizons of garnet quartzite, or garnet-
gahnite rocks, suggesting that lode horizons form an alteration halo related to the
emplacement or metamorphism of the sulphides. Two distinct styles of mineralisation were
observed in drill core, massive sulphide and vein style mineralisation. Massive sulphides
commonly have a composition sphalerite-galena>pyrrhotite>chalcopyrite compared to vein
style mineralisation which is typically pyrrhotite-chalcopyrite>galena-sphalerite. Vein
style mineralisation intersections of 1 Lens and to a lesser extent, the A Lode, consists of
low-grade stringer veins with the more mobile sulphides present such as galena and
pyrrhotite, whereas massive sulphides are higher-grade intersections, with an increased
abundance of the lesser mobile sulphides such as sphalerite. The texture of the massive
sulphide ore is coarse grained and commonly brecciated whereas vein style mineralisation
is more flow textured. Both suggest recrystallisation after initial prograde mineral growth.
31
Chapter Four – Sulphide Rock Geochemistry
Chapter Four - Sulphide Rock Geochemistry
4.1 Introduction During the course of fieldwork, a total of 43 rock samples from sulphide rocks were
collected comprising 24 samples as quarter NQ core samples, and eighth HQ core samples
and 19 bulk samples from the Kintore pit. These samples were analysed for major, trace,
rare earth and halide elements as well as carbon and oxygen isotopes, in order to document
and contrast the broad geochemistry of the individual ore lodes, and to identify trends
which may shed some light on their genetic evolution. The results from this study are
contrasted with various other results in the literature from studies of Broken Hill or other
comparable systems around the world. Where contrasted with data from this study, all 2
Lens and C Lode data has been sourced from Sproal (2001) and all Western Mineralisation
data has been sourced from Kitchen (2001).
4.2 Base Metal Geochemistry It has been well documented in the literature (Gustafson et al., 1950; Johnson and
Klingner, 1975) and observed in various mines at Broken Hill that the individual ore lodes
unique individual metal ratios. This holds true on CML7 (Table 4.2.1a and Appendix 3).
As documented in Chapter Three, there are two distinct styles of mineralisation, vein style
and massive style, each having unique mineralogy and this affects the overall geochemistry
of the individual ore lodes.
CML7 Broken Hill Historic Mining Ore Lode Pb wt% Zn wt% Ag g/t Pb wt% Zn wt% Ag g/t
Kintore Lode 16.4 16.0 169.6 - - - B Lode 5.8 12.1 82.6 4.4 12.5 35.0 A Lode 1.7 0.8 21.2 3.3 7.8 30.0 1 Lens 1.9 0.8 17.2 7.7 16.8 50.0
Western Min. 3.3 4.8 4.0 - - - C Lode 2.1 8.8 20.0 2.0 4.0 20.0 2 Lens 9.4 5.7 60.9 14.0 11.0 105.0 3 Lens 21.2 18.3 576.7 12.6 13.6 234.0
Table 4.2.1a: Average base metal abundance on CML7 and for Broken Hill historically (Broken
Hill historic mining figures from Laing, 1996).
32
Chapter Four – Sulphide Rock Geochemistry
Figure 4.1: Ternary plot of Pb-Zn-Ag/10 for
the 43 samples in this study from each of the
four sampled zinc lodes.
Figure 4.2: Ternary plot of the average Pb-Zn-
Ag/10 for all lodes on CML7. (3 Lens data
from Groombridge, 2002/03).
Figure 4.3: Ternary plot of average Pb-Zn-
Ag/10 mined at Broken Hill (after Laing,
1996).
Broad classification of the B Lode, A lode and 1 Lens has been as ‘zinc lodes’
based on the high Zn:Pb ratios in these lodes (Matthias, 1974). This is shown by most B
33
Chapter Four – Sulphide Rock Geochemistry
Lode samples with dominant Zn (Figure 4.1) or the Kintore Lode with approximately
equivalent Zn:Pb. Samples from A Lode and 1 Lens show enrichment in Pb and Ag rather
than Zn and is highlighted in the comparison between this studies ore lode average metal
ratios and those of the C Lode, 2 Lens and Western Mineralisation on CML7 (Figure 4.2)
and also with those from Laing (1996)(Figure 4.3) which were based on the historical
mining grades at Broken Hill. The Kintore Lode shows a wide distribution with no
dominant metal cation, however it also plots in a similar trend to A Lode and 1 Lens. Each
ore lode shows that the modal abundance of Pb, Zn, Ag and Cu decreases as the modal
abundance of silica increases (Figure 4.4) as the mineralisation changes from massive
sulphides to blue lode quartz-hosted stringer mineralisation.
SiO2 vs Pb
0
5
10
15
20
25
30
35
0 20 40 60 80 100
SiO2 vs Ag
0
50
100
150
200
250
300
350
0 20 40 60 80 100
SiO2 (wt%)
Ag
(g/t)
Kintore Lode B Lode A Lode 1 Lens
SiO2 (wt%)
Pb (w
t%)
Kintore Lode B Lode A Lode 1 Lens SiO2 vs Zn
0
5
10
15
20
25
30
35
0 20 40 60 80 100
SiO2 vs Cu
0
0.1
0.2
0.3
0.4
0.5
0 20 40 60 80 100
SiO2 (wt%)
Cu
(wt%
)
Kintore Lode B Lode A Lode 1 Lens
SiO2 (wt%)
Zn (w
t%)
Kintore Lode B Lode A Lode 1 Lens
Figure 4.4: Harker digrams for dominant metal cations showing negative trends with increasing silica.
4.3 Major Element Geochemistry Major elements (Appendix 4) were analysed by ICP-OES and ICP-MS techniques for the
43 rock samples. Elements analysed include Al, Ca, K, Fe, Mg, Mn, Na, P, Si and Ti
(Table 4.3.1a). Major elements are useful for identifying broad geochemical trends and
inter-element relationships in the rock samples and since all the samples were collected
34
Chapter Four – Sulphide Rock Geochemistry
from within ore lodes, major elements can be used in comparison with other previous
studies from metasediments in order to see if these trends are observed in both sets of data
therefore possibly constraining the orebody to a coeval evolution with surrounding
stratigraphic units.
Table 4.3.1a: Major element average abundances in order of modal abundance.
Ore Lode Major
Element Kintore Lode
(n=19) B Lode (n=9)
A Lode (n=9)
1 Lens (n=6)
SiO2 32.17 51.31 65.93 68.23 Fe2O3 10.14 10.10 14.86 14.55 Al2O3 5.06 5.36 8.41 8.65 MnO 3.70 0.54 1.87 1.20 CaO 2.34 2.16 1.11 0.30 P2O5 0.91 1.34 0.08 0.05 MgO 0.29 0.57 1.15 1.19 K2O 0.19 1.21 0.86 0.60 TiO2 0.14 0.20 0.36 0.36 Na2O 0.01 0.11 0.06 0.03
SiO2 vs MnO
0
2
4
6
8
10
0 20 40 60 80 100SiO2 (wt%)
MnO
(wt%
)
Kintore Lode B Lode A Lode 1 Lens 2 Lens
Si02 vs Al2O3
0
5
10
15
0 20 40 60 80 1Si02 (wt%)
Al2 O
3 (w
t%)
00
Kintore Lode B Lode A Lode 1 Lens 2 Lens
Figure 4.5: Harker diagram showing major element variation of all samples for MnO.
Figure 4.6: Harker diagram showing major element variation of all samples for Al2O3.
SiO2 vs CaO
0
5
10
15
20
25
0 20 40 60 80 100SiO2 (wt%)
CaO
(wt%
)
Kintore Lode B Lode A Lode 1 Lens 2 Lens
SiO2 vs Fe2O3
0
10
20
30
40
50
0 20 40 60 80 100SiO2 (wt%)
Fe2 O
3 (w
t%)
Kintore Lode B Lode A Lode 1 Lens 2 Lens Figure 4.7: Harker diagram showing major element variation of all samples for CaO.
35
Figure 4.8: Harker diagram showing major element variation of all samples for Fe2O3.
Chapter Four – Sulphide Rock Geochemistry
SiO2 vs K2O
0
1
2
3
4
5
0 20 40 60 80 100SiO2 (wt%)
K2O
(wt%
)
Kintore Lode B Lode A Lode 1 Lens 2 Lens
SiO2 vs Na2O
00.05
0.10.15
0.20.25
0.30.35
0 20 40 60 80 100SiO2 (wt%)
Na2
O (w
t%)
Kintore Lode B Lode A Lode 1 Lens 2 Lens Figure 4.9: Harker diagram showing major element variation of all samples for K2O.
Figure 4.10: Harker diagram showing major element variation of all samples for Na2O.
In modal order of abundance, the ore lodes (Table 4.3.1) are dominantly comprised
of Si, with enrichment in Fe, Al, Mn and Ca. Small amounts of P, Mg, Ti and Na complete
the major element composition of the samples. When plotted as Harker diagrams, there
were three distinct trends. There were vaguely parabolic trends such as MnO (Figure 4.5)
and Al2O3 (Figure 4.6) where the modal abundance of Mn and Al increased with
increasing Si up to an inversion point of approximately 50% silica, where the abundance of
the Mn and Al would decrease with further increasing Si. This trend was present for Al2O3,
MgO, MnO and to a lesser extent TiO2. These elements, with the exception of TiO2, are
major components of garnet, a primary constituent of the ore lode mineralogy as shown in
Chapter Three, with Al2O3 abundant in common garnet end-members and MgO and MnO
dominant in the end-members of pyrope (Mg3Al2Si3O12) and spessartine (Mn3Al2Si3O12)
respectively. Two other major element oxides, CaO (Figure 4.7) and Fe2O3 (Figure 4.8)
form two further end-members of garnet, almandine (Fe3Al2Si3O12) and grossular
(Ca3Al2Si3O12) respectively, and show negative trends in relation to increasing Si content.
The third trend is seen in K and Na (Figure 4.9 and 4.10), where there is a positive
relationship with increasing Si content, related to increasing alkali feldspar with increasing
Si. All other major elements show insignificant variation.
36
Chapter Four – Sulphide Rock Geochemistry
Major element abundance relative to metasediments
-50.00
-40.00
-30.00
-20.00
-10.00
0.00
10.00
20.00
SiO2 TiO2 Al2O3 Fe2O3 MnO MgO CaO Na2O K2O P2O5
Major elements
Rel
ativ
e A
bund
ance
(wt %
)
Kintore Lode Average B Lode Average A Lode Average 1 Lens Average Figure 4.11: Abundance of major elements of this study relative to those of Broken Hill
metasediments from Slack and Stevens (1994).
When compared to distal clastic metasediments from Broken Hill in Slack and
Stevens (1994), the averaged ore lode major element abundances in this study (Figure
4.11) show a pronounced depletion of Si, Al and K, with a strong enrichment of Fe and a
lesser enrichment of Mn and Ca.
Prominent trends within certain major element Harker plots have been inferred to
indicate the source of rock chemistry and therefore have been used to constrain genetic
models for Broken Hill (Slack and Stevens, 1994). They showed that major element
Harker diagrams of Broken Hill metasediments had linear negative trends and plotted
within a well-defined spatial field (Figure 4.12 and 4.13). They suggested this trend is
related to a large clastic component in these metasediments. Of the ore lodes observed in
this study, no Harker plots showed any linear features similar to that of Slack and Stevens
(1994) or correlation with the field of clastic metasediments for the elements Al and Fe
(Figure 4.12 and 4.13).
37
Chapter Four – Sulphide Rock Geochemistry
Figure 4.12: Comparison of Al2O3
Harker plot for this study (in
colour) showing no correlation
with those of Slack and Stevens
(1994) that are inferred to indicate
the field of clastic metasediments.
EPCM represents average Early
Proterozoic clastic metasediments
(from Taylor and McLennan,
1985).
Figure 4.13: Comparison of Fe2O3
Harker diagrams of this study (in
colour) showing no correlation
with those of Slack and Stevens
(1994) inferred to indicate the
field of clastic metasediments.
EPCM represents average Early
Proterozoic clastic metasediments
(from Taylor and McLennan,
1985).
4.4 Trace Element Geochemistry Trace elements (Appendix 5) were analysed by ICP-OES and ICP-MS techniques for the
43 rock samples. Elements analysed were Ba, Cr, V, As, Bi, Sb, Th, Y, Sr, W, Rb, Co, Cd,
U, Zr, Ta, Nb and REE (Table 4.4.1a). Trace elements typically comprise up to 1% of the
rock.
The ore lodes, especially the Kintore Lode, exhibit an enrichment in As. It has been
noted by a number of authors that As accumulates at the extremity of a given orebody, and
38
Chapter Four – Sulphide Rock Geochemistry
this is the case with the Kintore Lode samples. The Kintore Lode is also enriched with Cd,
Sb and Co while being depleted in Zr, Rb and U. The B Lode exhibits an anomalously high
enrichment of Ba, V, Rb and U and a depletion of Co and Nb. The A Lode and 1 Lens are
enriched in Ba, Zr and Th while 1 Lens was the only ore lode that contained Y. Ta is
absent from all lodes.
Table 4.4.1a: Trace element average abundances in order of modal abundance.
Ore Lode Trace
Element Kintore Lode
(n=19) B Lode (n=9)
A Lode (n=9)
1 Lens (n=6)
As 1744.74 377.22 264.44 393.33 Ba 160.00 360.00 210.00 152.50 V 45.38 600.00 36.25 35.00
Cd 400.38 30.00 26.00 15.00 Sb 201.95 124.00 23.11 84.17 Zr 35.38 100.00 126.25 170.00 Rb 14.31 110.00 49.56 48.88 Cr 68.46 50.00 55.00 40.00 U 4.38 105.00 3.50 3.75
Co 48.46 0.00 22.50 30.00 Sr 44.23 40.00 10.63 5.00 W 24.38 12.00 5.50 4.00 Th 5.74 7.33 17.39 15.17 Bi 5.58 21.67 8.00 2.33 Nb 2.69 0.00 3.75 2.50 Y 0.00 - - 6.50 Ta 0.00 0.00 0.00 0.00
When compared to distal clastic metasediments from Broken Hill from Slack and
Stevens (1994), the averaged ore lode trace element abundances in this study show a
pronounced depletion of Rb, Ba, Y and Zr, with a minor enrichment of U and Co. B lode
showed an anomalously high enrichment of V (Figure 4.14).
39
Chapter Four – Sulphide Rock Geochemistry
Trace element abundance relative to metasediments
-600.00
-400.00
-200.00
0.00
200.00
400.00
600.00
Rb Sr Ba Y Zr Nb Ta Th U V Co
Trace Elements
Rel
ativ
e A
bund
ance
(ppm
)
Kintore Lode Average B Lode Average A Lode Average 1 Lens Average Figure 4.14: Abundance of trace elements of this study relative to those of Broken Hill
metasediments from Slack and Stevens (1994) where comparable.
4.5 Rare Earth Element Geochemistry Although classified as trace elements and present in similar quantities, rare earth elements
(REE) of the lanthanide series are commonly treated separately due to their unique,
uniform chemical properties resulting from their electronic configurations (Henderson,
1984). REE initially have been used with great success in igneous petrology, and although
their chemical properties are alike, individual REE can be fractionated by various
petrological and mineralogical processes (Henderson, 1984).
Trends related to the abundance of REE in igneous rocks are able to give an
indication of the partial melting, fractional crystallisation and mixing pathways that have
occurred for the genesis of a given igneous rock (Haskin, 1984). Rare earth elements are
generally considered to be immobile except under extreme hydrothermal conditions or
retrogression and only when there is a tremendous amount of fluid flow and long residency
times (Lottermoser, 1992; Bierlein, 1995). REE trends can be applied to hydrothermal
systems where it has been shown that REE signatures reflect the primary hydrothermal
physico-chemical conditions (Lottermoser, 1992; Klinkhammer et al., 1994; Bierlein,
1995). Hydrothermal fluids from a number of modern systems including the Red Sea
(Courtois and Treuil, 1977 in Lottermoser, 1989) (Figure 4.15), the East Pacific Rise
(Michard et al., 1983; Michard and Albarede, 1986) (Figure 4.16), the Southern Explorer
Ridge (Barrett et al., 1990) and the TAG Mound on the Mid-Atlantic Ridge (Mills and
40
Chapter Four – Sulphide Rock Geochemistry
Elderfield, 1995) show similar REE signatures. Comparable signatures have been observed
in Paleoproterozoic Australian hydrothermal systems including the Broken Hill orebody
(Lottermoser, 1989; Slack and Stevens, 1994)(Figure 4.17), the Pinnacles deposit (Parr,
1992a) and Cannington (Bodon, 1996).
Figure 4.15: Hydrothermal fluid REE
signature from Red Sea and Romanche
Fracture Zone (Courtois and Treuil, 1977;
Bonatti et al., 1976 in Lottermoser, 1989).
Figure 4.16: Hydrothermal fluid REE
signature from East Pacific Rise and of
seawater (Michard and Albarede, 1986;
Goldberg et al., 1969 in Lottermoser, 1989).
Figure 4.17: REE signatures from
proximal exhalites and sulphide ore
at Broken Hill and proximal
exhalites from other Broken Hill-
type deposits (Lottermoser, 1989).
41
Chapter Four – Sulphide Rock Geochemistry
All of the 43 samples collected in fieldwork were analysed by ICP-MS for REE
(Appendix 6). The abundances were then normalised against the values for Average C1
Chondrites (Boynton, 1984) and against the North American Shale Composite
(NASC)(Piper, 1974). Normalisation of REE is necessary to limit the variations between
odd and even REE and provides a comparative benchmark for REE studies. C1 Chondrites
are thought to represent the primordial solar nebula composition (Boynton, 1984) whereas
the NASC represents the average concentration of REE in sediments based on 40 shales in
America which are suggested to be equivalent to the average abundance of REE in the
upper crust as a result of the homogenisation of original igneous REE abundances (Fleet,
1984). REE tends, when normalised against NASC, tend to show a flatter profile
comparative to C1 Chondrite normalised trends.
CML7 Ore Lode REE
1
10
100
1000
La Ce Pr Nd Sm Eu Gd Tb Dy Ho Er Yb Lu
Rare Earth Elements
Cho
ndrit
e N
orm
alis
ed A
bund
ance
Kintore Lode (n=19) B Lode (n=9) A Lode (n=9) 1 Lens (n=6)3 Lens (n=6) C Lode (n=8) 2 Lens (n=9) Western Min. (n=14)
Figure 4.18: Chondrite normalised average REE abundance for all ore lodes on CML7.
42
Chapter Four – Sulphide Rock Geochemistry
CML7 Ore Lode REE
0.01
0.1
1
10
La Ce Pr Nd Sm Eu Gd Tb Dy Ho Er Yb Lu
Rare Earth Elements
NA
SC N
orm
alis
ed A
bund
ance
Kintore Lode (n=19) B Lode (n=9) A Lode (n=9) 1 Lens (n=6)3 Lens (n=6) C Lode (n=8) 2 Lens (n=9) Western Min. (n=14)
Figure 4.19: NASC normalised average REE abundance for all ore lodes on CML7.
The B Lode, A Lode and 1 Lens show LREE enrichment with distinctive Eu
anomalies for the chondrite-normalised samples (Figure 4.18) and a flatter profile with
significant Eu anomalies when NASC-normalised (Figure 4.19). The Eu/Eu* anomaly was
calculated from McLennan’s formula (McLennan, 1989) for all samples and ranged from
0.37 to 4.32 indicating both positive (27 samples) and negative (16 samples) anomalies.
The extent of the Eu anomaly, appears linked to the abundance of CaO compared to Eu
(Figure 4.20) as the gradient is steeper for ore lodes that exhibited the higher Eu anomalies.
Eu vs CaO
0
5
10
15
20
25
0 5 10 15
Eu (ppm)
CaO
(wt%
)
Kintore LodeB LodeA Lode1 LensTS&IP C LodeTS 2 LensKK Western MinLinear (A Lode)Linear (Kintore Lode)Linear (B Lode)Linear (TS 2 Lens)Linear (1 Lens)
Figure 4.20: Eu vs CaO for all CML7 ore lodes with positive Eu anomaly ore lodes with
steeply trending gradients and negative anomaly Eu anomalies with flat gradients.
43
Chapter Four – Sulphide Rock Geochemistry
The Ce/Ce* anomaly of Toyoda and Masuda (1991) ranged from 0.79 to 1.36
including 19 samples with no anomaly, 19 samples with negative anomalies and 5 samples
with positive anomalies.
4.6 Carbon and Oxygen Isotope Geochemistry The Broken Hill orebody has been deformed by late stage fault-constrained fluids that have
resulted in the formation of new carbonate and other minor minerals within the fault zones
and in fracture planes extending out from the faults. It has been documented that individual
lodes exhibit carbonate-bearing faults and microfractures (Lawrence, 1968; Plimer, 1984).
With stable isotope analytical techniques, carbonate veins can be useful in indicating the
origins of fluids interacting with the orebodies and for the relative dating of various
episodes in the deformation history. Of the previous carbon and oxygen isotope studies at
Broken Hill, some have focussed on the analysis of secondary minerals within the oxidised
zone of the orebody (Böttcher et al., 1993; Melchiorre et al., 1999, 2000) whereas others
have focussed on the analysis of carbon-bearing prograde ore lode minerals (Sproal, 2001)
or of broad isotope variation within the Broken Hill Block (Cartwright, 1999).
δ18O vs δ13C
-50
-45
-40
-35
-30
-25
-20
-15
-10
-5
00 5 10 15 20 25 30 35
δ18O (‰ vs. SMOW)
δ13C
(‰ v
s. P
DB)
2 Lens Fault zone Secondary malachite B Lode microfractures (this study)Rhodochrosite-smithsonite
Figure 4.21: δ18O and δ13C isotope analyses from B Lode microfractures with comparison
to other stable isotope analyses at Broken Hill including 2 Lens (Sproal, 2001), oxidised
zone rhodochrosite-smithsonite (Böttcher et al., 1993) and malachite (Melchiorre et al.,
1999) and fault zones (Gallacher, 1995).
44
Chapter Four – Sulphide Rock Geochemistry
The carbon and oxygen isotope analyses from B Lode microfractures in this study
(Figure 4.21) were completed at Monash University using a Finnigan-Matt 252 mass
spectrometer. Carbon isotopes results ranged from -13.7 to -14.1 (% vs. PDB) and oxygen
isotopes range from 27.7 to 31.4 (% vs. SMOW) indicating a biogenic source for the
carbon.
4.7 Halogen Geochemistry Halogens are strongly fractionated by various geological processes and as a result are
useful in determining the evolution of fluids and mixing processes within the crust (Bohlke
and Irwin, 1992). They are commonly the primary complexing mechanism for metal
transport (Large et al., 1996) and therefore are of importance to the genetic evolution of
orebodies.
The halogens Cl, F, Br and I are contained within secondary minerals within the
oxidised zone of the Broken Hill main lode orebody (Lawrence, 1968) which generally
extends down 120m from the surface but is present to 610m in highly fractured zones (van
Moort and Swensson, 1982). Common primary minerals are fluorite (CaF2), fluorapatite
(Ca5(PO4)3F), fluorapophyllite ((KCa4Si8)20(F,OH).8H20) and secondary minerals are
iodargyrite (AgI), chloroargyrite (AgCl) and bromargyrite (AgBr). The 43 samples were
analysed for Cl and F by ICP-OES (Appendix 6). Br and I are unable to be analysed by this
method.
F
0
0.05
0.1
0.15
0.2
0.25
0.3
0.35
0.4
0.45
WesternMin.
C Lode B Lode A Lode KintoreLode
1 Lens 2 Lens 3 Lens
Ore Lode
F (w
t%)
F
Cl
0
50
100
150
200
250
300
350
400
WesternMin.
C Lode B Lode A Lode KintoreLode
1 Lens 2 Lens 3 Lens
Ore Lode
Cl (
ppm
)
Cl
Figure 4.22: F and Cl average abundances for the individual ore lodes on CML7.
The average abundances of F and Cl for the individual ore lodes on CML7 (Figure
4.22) show an increasing abundance of both F and Cl in B Lode. This is followed by
relatively low abundances in A Lode, the Kintore Lode and 1 Lens.
45
Chapter Four – Sulphide Rock Geochemistry
4.8 Discussion The zinc lodes, (B Lode, A lode and 1 Lens) all show unique metal ratios. The A Lode and
1 Lens samples are somewhat atypical (Figure 4.2 cf. Figure 4.3) to previously
documented metal ratios from historical mining at Broken Hill (Laing, 1996). This results
from the drill intersections of low-grade vein style mineralisation which is rich in mobile
sulphides including galena (Marshall and Gilligan, 1987) and hence has a high Pb:Zn ratio.
This enrichment in Pb may be a consequence of the remobilisation of sulphides during
deformation as suggested by Maiden (1976) and Plimer (1984, 1987). The B Lode and
Kintore Lodes show more typical Zn:Pb ratios commensurate with previous documentation
of the zinc lodes at Broken Hill (Laing, 1996), yet both are rich in Pb and/or Zn and Ag
compared to historic mining data. The abundance of all metals decreases with increasing
SiO2 (Figure 4.4) with changes from massive sulphides to quartz hosted disseminated
mineralisation.
The major element geochemistry of the ore lodes comprises Si, Fe, Al, Mn, and Ca
(Table 4.3.1) reflecting the abundance of garnet and quartz, the two must abundant gangue
minerals within the ore lodes. Some trends were vaguely parabolic such as MnO (Figure
4.5) and Al2O3 (Figure 4.6) where the modal abundance of Mn and Al increased with
increasing Si, to a point of approximately 50% silica where the abundance of the Mn and
Al decreases with further increasing Si. This trend was observed for Al2O3, MgO, MnO
and to a lesser extent TiO2. This may indicate that pyrope and spessartine garnets are
present in only a low abundance in both low and high Si assemblages and present in much
higher abundances in moderate Si assemblages. TiO2 shares a similar trend as it is
commonly found substituting into garnet, in this case substituting preferentially into
pyrope and spessartine garnet. Two other major element oxides, CaO (Figure 4.7) and
Fe2O3 (Figure 4.8) which form two further end-members of garnet, almandine
(Fe3Al2Si3O12) and grossular (Ca3Al2Si3O12) show negative trends in relation to increasing
Si content. This indicates that these garnets are more abundant in low Si assemblages. Fe is
also contained within sulphide minerals pyrrhotite and chalcopyrite and the decrease of
these minerals as Si increases may be the source of the observed trend for Fe. When
compared to major element abundances of Broken Hill Block metasediments (Figure 4.11),
the ore lodes are enriched in Fe, Mn and Ca, but deficient in Si, Al and K. The enrichment
in Fe, Mn and Ca is likely to be the result of increased garnet growth within the ore lodes
46
Chapter Four – Sulphide Rock Geochemistry
while the depletion of Al and K is likely to be the result of decreased biotite and sillimanite
in the ore lodes relative to the pelitic to psammitic metasediments.
Slack and Stevens (1994) suggested that major elements in clastic metasediments
show linear negative trends and plot within a well-defined spatial field. On CML7, the C
Lode has been interpreted as containing a high abundance of clastic sediments by Sproal
(2001) on the basis of this association, while Kitchen (2001) showed that the Western
Mineralisation contained no linear features in the data and therefore contained no clastic
input. The major element geochemistry of the B Lode, A Lode and 1 Lens shows no
correlation with those of clastic metasediments from Slack and Stevens (1994) when
contrasted in Figures 4.12 and 4.13. This provides strong evidence that ore lodes are not
hosted in clastic metasedimentary lithologies as suggested by Wright et al. (1987) for their
syngenetic sedimentary model for the orebody genesis. This also provides evidence that
the orebody did not form by the preferential replacement of sedimentary and volcanic
lithologies by sulphide rocks, as is the case in suggested epigenetic replacement models
(Gustafson et al., 1950).
Trace elements are highly variable between and within the ore lodes (Table 4.4.1),
and commonly are the result of substitutions within the framework of existing minerals,
likely to have occurred during metamorphism. When compared to clastic metasediment
trace element abundances, the zinc lodes show a pronounced depletion of Rb, Ba, Y and Zr
and slight enrichment of Co. The depletion may be due to a lack of detrital zircons and
other accessory minerals such as rutile and monazite, which give anomalously high
abundances within the surrounding metasediments and metavolcanics (Slack and Stevens,
1994). This may provide further evidence that indicates the ore lodes and enclosing lode
horizon rocks are significantly different to the surrounding metamorphosed and altered
metasediments.
The ore lodes exhibit REE signatures similar to a number of comparable ancient
orebody systems around the world, as well as being similar to modern systems. They
exhibit enrichment in light REE and depletion in heavy REE. A negative Ce anomaly was
common in the majority of samples, indicating interaction with seawater and a leaching of
Ce during deposition (Toyada and Masuda, 1991). The ore lodes contain both negative and
positive Eu anomalies, which may be related to the oxidation state of deposition related to
changes in temperature and pH, causing instability of the Eu3+ variety under high
temperature or reducing conditions compared to the Eu2+ variety (Sverjensky, 1984; Taylor
and McLennan, 1985; Michard and Albarede, 1986; Lottermoser, 1989). Therefore ore
47
Chapter Four – Sulphide Rock Geochemistry
lodes with positive Eu anomalies (3 Lens, 2 Lens, B Lode, Kintore Lode) may have formed
via the exhalation of hot (>250oC), reducing hydrothermal fluids with no clastic input
whereas the ore lodes with negative Eu anomalies (Western Mineralisation, C Lode, A
Lode, 1 Lens) formed via the exhalation of colder (200-250oC), more oxidising
hydrothermal fluids, possibly with intercalated clastic input. It is also noted that in
accordance with Goldschmidt’s Rules, Eu can substitute for other similar size elements
such as Ca (Figure 4.20). It can be seen that ore lodes with highest amounts of Ca/Eu also
have positive Eu anomalies and this is proportional to the size of the anomaly. Therefore it
is suggested that the amount of Ca-Eu substitution has a significant bearing on the Eu
anomaly. REE in the B Lode, A Lode and 1 Lens are comparable to ancient Broken Hill-
type deposits Cannington (Australia)(Bodon, 1996), Bergslagen (Sweden)(Plimer, 1988)
and Gamsberg (South Africa). These ancient systems have modern analogues with
comparable REE signatures in exhaling hydrothermal fluid, in the form of the Red Sea
(Figure 4.15), East Pacific Rise (Figure 4.16), TAG Mound on the Mid-Atlantic Ridge and
the Southern Explorer Ridge.
The close proximity of the carbon and oxygen isotopes of this study (Figure 4.21)
to those of supergene secondary minerals from Bottcher et al. (1993) and Melchiorre et al.
(1999) suggest a common source, and as mentioned by Gallacher and Plimer (2001) could
be from descending fluids containing oxidised biogenic carbon. Gallacher and Plimer
(2001) suggest that these fluids are the result of ascending fault bound fluids with carbon
sourced from the underlying carbonaceous sequences of the Paragon Group. It is suggested
that the carbonate minerals contained within the B Lode microfractures share a chemical
affinity with secondary minerals in the oxidised zone. However since they occur below the
primary oxidation zone, and no evidence was observed of oxidation in drill core at the
depth of the B Lode, it is suggested that the secondary minerals are the result of ascending
biogenic carbon-bearing fault bound fluids.
The average abundances of F and Cl for the individual ore lodes on CML7 (Figure
4.22) suggest that there is an increasing abundance of both F and Cl in the early stages of
the orebody formation from the Western Mineralisation, C Lode and B Lode. This is
followed by relatively low abundances in A Lode, the Kintore Lode and 1 Lens. 2 Lens has
anomalously high levels of both F and Cl while 3 Lens had relatively low abundances. It is
possible that F and Cl levels are related to the initial start up phases of the hydrothermal
system seen by high levels in the Western Mineralisation, C Lode and 2 Lens. There does
not appear to be a correlation between high-grade ore lodes and the abundances of F and Cl
48
Chapter Four – Sulphide Rock Geochemistry
as the high grade Kintore Lode has low abundances. Studies have shown that variations in
F and Cl within apatite from magnetite-apatite ore bodies in Chile can be used to constrain
genetic evolution to hydrothermal fluids or magma mixing with P-rich aqueous fluids
(Treloar and Colley, 1996). Another study (Bohlke and Irwin, 1992) has documented the
implications of halogens in fluid inclusions and used these to contrast the sources of fluid
salinity within various hydrothermal systems. Further work needs to be carried out at
Broken Hill to see if the occurrence of halogens at Broken Hill is related to the ore forming
processes or if they are from a later unrelated source. If halides are conclusively linked to
ore forming processes in Broken Hill-type deposits, they may become an important
exploration target in regolith geochemistry due to their relatively mobility and tendency to
diffuse to the surface.
49
Chapter Five – Sulphide Rock Petrography
Chapter Five - Sulphide Rock Petrography 5.1 Introduction A total of 25 polished and one thin section were produced from the samples taken from
core and pit. These sections were observed under reflected and transmitted light using a
Nikon Labophot2-Pol polarising microscope and petrographic observations noted.
Photomicrographs were taken of most minerals and of any features of interest identified
such as metamorphic and deformation features and remobilisation textures within these
sections.
5.2 Polished Section Microscopy 5.2.1 Introduction
The mineralogy of the individual zinc lodes was generally consistent, however the modal
abundance of the mineralogy varied quite considerably (Tables 5.2a-d). On average,
gangue minerals comprised 50% of the B Lode and Kintore samples, while in the A Lode
and 1 Lens, sulphide minerals accounted for 25% and 30% of the total modal abundance of
the sections. The 25 polished sections were taken from the ore lodes including B Lode (6),
A Lode (10) and 1 Lens (4) core samples and from the Kintore Lode (5) pit samples. The
single unpolished section was taken from a sample of spotted pelite metasediment prior to
the ore lodes. In Tables 5.2a-d, an abundance denoted as <5% means that the mineral was
only rarely observed while prograde and/or retrograde refers to the inferred period of
growth for the given mineral.
Table 5.2a: Mineralogy of B Lode in average modal abundance.
Sulphide Minerals (50%) Gangue Minerals (50%)
Sphalerite 50% Prograde/retrograde Quartz 80% Prograde/retrograde
Galena 25% Prograde/retrograde Garnet 10% Prograde/retrograde
Pyrrhotite 20% Prograde/retrograde Biotite 5% Prograde/retrograde
Chalcopyrite 5% Prograde/retrograde Chlorite 5% Retrograde
Pyrite <5% Retrograde Muscovite <5% Retrograde
Gudmundite <5% Retrograde Carbonates <5% Retrograde
50
Chapter Five – Sulphide Rock Petrography
Table 5.2b: Mineralogy of A Lode in average modal abundance.
Sulphide Minerals (25%) Gangue Minerals (75%)
Sphalerite 50% Prograde/retrograde Quartz 60% Prograde/retrograde
Pyrrhotite 40% Prograde/retrograde Garnet 15% Prograde/retrograde
Chalcopyrite 10% Prograde/retrograde Biotite 15% Prograde/retrograde
Galena <5% Prograde/retrograde Gahnite 10% Prograde
Arsenopyrite <5% Retrograde Chlorite <5% Retrograde
Table 5.2c: Mineralogy of 1 Lens in average modal abundance.
Sulphide Minerals (30%) Gangue Minerals (70%)
Galena 40% Prograde/retrograde Quartz 65% Prograde/retrograde
Sphalerite 35% Prograde/retrograde Garnet 15% Prograde/retrograde
Pyrrhotite 15% Prograde/retrograde Gahnite 15% Prograde
Chalcopyrite 10% Prograde/retrograde Biotite 5% Prograde/retrograde
Tetrahedrite <5% Retrograde Muscovite <5% Retrograde
Gudmundite <5% Retrograde
Arsenopyrite <5% Retrograde
Table 5.2d: Mineralogy of Kintore Lode in average modal abundance.
Sulphide Minerals (50%) Gangue Minerals (50%)
Sphalerite 40% Prograde/retrograde Quartz 70% Prograde/retrograde
Galena 30% Prograde/retrograde Garnet 20% Prograde/retrograde
Pyrrhotite 10% Prograde/retrograde Biotite 5% Prograde/retrograde
Chalcopyrite 10% Prograde/retrograde Chlorite 5% Retrograde
Arsenopyrite 10% Retrograde Muscovite <5% Retrograde
5.2.2 Sulphide Minerals
Sphalerite - ZnS
Sphalerite is the most abundant sulphide mineral in the rocks studied, with modal
abundances ranging from 30% to 50%. This supports the high Zn:Pb ratio within the zinc
lodes. In reflected light, sphalerite is dark grey, while in transmitted light appears an
opaque dark grey colour or when mildly oxidised, a red-brown colour as in the Kintore
Lode. Sphalerite occur as subhedral to anhedral grains of various sizes from 100µm to
51
Chapter Five – Sulphide Rock Petrography
4mm, although the average size is 1mm. Sphalerite commonly contains exsolution
lamellae of pyrrhotite and chalcopyrite and inclusions of sulphides including galena,
pyrrhotite, chalcopyrite and arsenopyrite (Figure 5.8) and rarely prograde gangue minerals
such as quartz (Figure 5.12), garnet and biotite. It has no distinct cleavage but in some
sections is fractured (Figures 5.5 and 5.15), suggesting it is more competent and less easily
deformed than the other sulphides. It has replaced prograde biotite in some places (Figure
5.19) and, in others, is replaced by biotite (Figure 5.20). It is prominent within massive
sulphides but rare within vein style mineralisation suggesting higher ore grade conditions
are required in order to mobilise it compared to other sulphides.
Galena - PbS
Galena is the second most abundant sulphide mineral within the B Lode and 1 Lens,
comprising between 25-40% of the total sulphides for a given lode, however it was
significantly lower to almost non-existent in the A Lode samples. The cleavage is
commonly curvilinear (Figure 5.2). The cleavage orientation between two adjacent crystals
can be highly variable within massive sulphides indicating subgrain rotation, but is more
uniform in orientation when occurring in narrow vein style mineralisation indicating
crystallisation in a more homogenous stress regime. The crystals vary from anhedral to
subhedral, of a large average size between 1.8mm and 4.5mm and occur as seriate
aggregates with other sulphide minerals. In many places small elongate galena crystals fill
interstices between other grains (Figure 5.12) and fractures within both garnet and gahnite
porphyryblasts and quartz (Figure 5.11), indicating late crystallisation or remobilisation
after deformation which has resulted in the fracturing of the more competent gangue
minerals. Galena has undergone replacement by chlorite in B Lode and replacement to
both biotite and to chlorite in A Lode. In 1 Lens, galena hosts tetrahedrite and associated
breakdown minerals chalcopyrite and gudmundite (Figure 5.25).
Pyrrhotite – Fe(1-x)S
Pyrrhotite is the third most abundant sulphide mineral within the zinc lodes, however it is
significantly lower than sphalerite or galena, comprising between 10% and 20% except in
the A Lode samples where it reached as high as 40%. It is commonly oxidised producing
an iridescent light gold colour (Figure 5.18). It can occur as subhedral crystals but is more
common as large anhedral singular grains approximately 1.8mm in size. Pyrrhotite is
mobilised by crosscutting late stage carbonate veins (Figure 5.18). Pyrrhotite can form
52
Chapter Five – Sulphide Rock Petrography
veins in its own right that crosscut other sulphide minerals (Figure 5.15). Like galena,
pyrrhotite commonly fills interstices between other crystals and fractures within other
minerals (Figure 5.13) indicating it is a relatively ductile sulphide.
Chalcopyrite - CuFeS2
Chalcopyrite is found in all of the zinc lodes in a consistently low abundance of between
5% and 10%. Chalcopyrite occurs primarily in three different styles. It can occur as
preferentially elongate minute exsolution lamellae within quartz (Figure 5.7) and
inclusions in both gangue and sulphide minerals (Figure 5.9) or as small grains of 100-
500µm at the edge of other sulphide crystals. It can fill interstices between other euhedral
to subhedral crystals in a deformed, remobilised texture commonly in association with
galena (Figure 5.14). Chalcopyrite is rarely contained within very fine folded micro-
fractures within quartz (Figure 5.8) indicating it is almost as ductile as pyrrhotite and
galena. In some places chalcopyrite is related to the breakdown of tetrahedrite in
association with gudmundite (Figure 5.25).
Arsenopyrite - FeAsS
Arsenopyrite is a rare sulphide in the zinc lodes, with minor amounts in 1 Lens and up to
10% in the Kintore Lode. Arsenopyrite increases towards the periphery of the ore lodes at
Broken Hill. In reflected light arsenopyrite is a bright light grey-pink colour, somewhat
similar to galena except without the triangular pits or cleavage. It is commonly euhedral
and has a higher relief than the other sulphide minerals. It varies greatly in size, with most
grains being approximately 100µm with rare crystals up to 1mm. In the Kintore Lode,
arsenopyrite occurs commonly as tiny inclusions within sphalerite in a similar way as
chalcopyrite (Figure 5.9). It also occurs as euhedral grains overgrowing garnet, quartz and
galena (Figure 5.10) or occupying interstices between gangue minerals in a strong
association with chalcopyrite (Figure 5.13).
Pyrite - FeS2
Pyrite is a rare sulphide in the Broken Hill ore lodes. It was identified in late stage
microfractures within the B Lode in association with carbonate vein minerals. It is a dull
yellow colour similar to pyrrhotite but forms small strongly subhedral to euhedral crystals.
It may result from the interaction of pyrrhotite with late stage vein fluids which took up
53
Chapter Five – Sulphide Rock Petrography
iron in the formation of siderite (FeCO3) at the edges of the veins, leaving excess sulphur
and remaining iron within the veins, forming pyrite.
Tetrahedrite - Cu12Sb4S13
Tetrahedrite is a rare mineral and in terms of the zinc lodes, is found only within the 1
Lens at an abundance of up to 5%. It is a light grey to green colour in reflected light and is
in association with galena and chalcopyrite (Figure 5.25). It is hard to distinguish from the
other grey sulphides due to its small size. At Broken Hill it is argentian tetrahedrite,
freibergite ((Ag,Cu)10(Zn,Fe)2[S|((Sb,As)S3)4]). It forms anhedral to subhedral crystals at
the boundaries of galena and is associated with chalcopyrite and gudmundite. This has
been suggested (Lawrence, 1968) to be a consequence of the retrograde breakdown of
silver-rich tetrahedrite which results in the formation of chalcopyrite, gudmundite as well
as sphalerite, lollingite and silver-deficient tetrahedrite and a number of silver minerals
including pyrargyrite, polybasite, stephenite and argentite. None of these silver minerals
were observed.
Gudmundite - FeSbS
Gudmundite is rare, occurring primarily in 1 Lens, in association with tetrahedrite and
chalcopyrite and also in B Lode without associated tetrahedrite. Under reflected light it is
white in colour, and is observed in very small anhedral to subhedral crystals while the
larger crystals can be euhedral (Figure 5.25). It is one of the non-silver derivatives from the
retrograde breakdown of tetrahedrite, with chalcopyrite being another. The presence of
gudmundite in B Lode suggests that tetrahedrite may have been present initially.
5.2.3 Gangue Minerals
Quartz - Si02
Quartz is the most prevalent gangue mineral in all lodes, ranging from 50% to 85% modal
abundance of the gangue minerals. In transmitted light it commonly has a low to moderate
relief, however it can exhibit many fractures (Figure 5.4) or fluid inclusions and exsolution
lamellae (Figures 5.7 and 5.8). It may also occur completely within sulphide minerals or
garnet and gahnite minerals. It has a broad size range from 500µm to 2mm variable across
all ore lodes. It is euhedral to subhedral shape, but in some places is brecciated with
angular edges within a sulphide matrix (Figure 5.4), particularly within the Kintore Lode
and B Lode. It appears the most euhedral and equigranular when it occurs in association
54
Chapter Five – Sulphide Rock Petrography
with vein style mineralisation observed in some of the A Lode sections. Late stage
carbonate veins crosscut quartz (Figure 5.22).
Garnet - (Mn Fe, Ca)3Al2(SiO4)3
Garnet (10% and 30% abundance), occurs most abundant within or adjacent to massive
sulphides and within the vein style mineralisation. It ranges in size from 200µm in vein
style sections to a maximum of 900µm in the massive sulphide sections. It is isotropic, has
a high relief mottled appearance and is slightly pink in colour under transmitted light. It
occurs predominately poikioblastic with the individual crystals having a euhedral to
subhedral shape and an association with biotite, sulphides and gahnite (Figure 5.7). It can
contain fluid inclusions or inclusions of quartz suggesting growth over quartz or may be
fractured with fractures often filled by sulphides. It some places, it may occur as thin rims
around gahnite (Figure 5.24).
Gahnite - ZnAl2O4
The zinc spinel gahnite occurs sporadically within the A Lode and 1 Lens, ranging from
10% to 15%, but is absent from the B Lode and Kintore Lode sections. Although similar to
garnet in texture, isotropy, shape and size, it is characterised by its higher relief and green
colour under transmitted light. Similar to garnet, it occurs as poikioloblastic grains and is
commonly highly fractured or has quartz crystals in the centre of the gahnite. In many
places the edges of the gahnite grains have been altered to fine grained muscovite, whereas
on other grains, thin garnet rims are present (Figure 5.24).
Biotite - K(Fe, Mg)3AlSi3O10(F, OH)2
Biotite occurs in low abundance across all of the zinc lodes, from 5% to 15% abundance.
Biotite grains are commonly small, subhedral to anhedral and platey when structurally
bound by more competent minerals such as quartz and sulphides. It is a common mineral
within the pelitic metasediments at Broken Hill (Figure 5.1) and within the ore lodes is
commonly associated with garnet, gahnite and sulphide minerals (Figure 5.7). Biotite is
rarely present completely surrounded by sulphide minerals, occurring as unaltered euhedral
crystals, suggesting prograde mineral growth. In some places it is overgrown by sphalerite
(Figure 5.18). Other examples have been completely or partially retrograded to muscovite
(Figures 5.20 and 5.21).
55
Chapter Five – Sulphide Rock Petrography
Muscovite - KAl2(AlSi3O10)(OH)2
Muscovite is present in low abundances of <5% within the B Lode and 1 Lens. It is also
present in high abundances within pelite outside of the ore lodes (Figure 5.1). Within the
ore lodes it primarily exists as small platey crystals. It occurs around the edges of biotite
minerals or completely pseudomorphs them as a result of retrogression (Figures 5.20 and
5.21).
Chlorite - (Fe, Mg, Al)6(Si, Al)4O10(OH)8
Chlorite is another rare gangue mineral within the zinc lodes, primarily occurring as a
result of the retrogression of biotite within the A Lode and Kintore Lode. It resembles
biotite in shape and form but is a transparent or green to yellow in colour. It is likely that it
was present in the B and 1 Lens, but has been further retrogressed to muscovite.
Carbonates – (Ca, Fe, Mg)CO3
Late stage carbonate veins crosscut the B Lode and the minerals contain fine angular grains
which crosscut various other minerals. The carbonate mineral species were only
conclusively determined later by electron microprobe analysis as siderite (FeCO3), calcite
(CaCO3) and magnesite (MgCO3). Siderite is one of the most common minerals in
Delamerian remobilised shear zone ore at Broken Hill (Lawrence, 1968). The veins
commonly contain pyrite (Figures 5.5, 5.17 and 5.22) and included grains of quartz and
other sulphides including sphalerite entrained during vein propagation through the rock.
Under transmitted light they appear mottled dark green to black, fine grained with distinct
layers from the boundary of the vein to the centre.
5.3 Paragenesis 5.3.1 Introduction
The Broken Hill main lode orebody has undergone the same intense and sustained
metamorphic and deformation history as the whole Broken Hill Block described in Chapter
Two. The results of the complex geological history have already been seen on a regional
scale, a macroscopic scale in core and pit samples and are present on a microscopic scale.
The mineral assemblages have preserved some deformation features, metamorphic
features, remobilisation features and retrogression features described in Section 5.2.
56
Chapter Five – Sulphide Rock Petrography
5.3.2 Deformation and Metamorphism Features
Qtz
Ga Sill
400µm 550µm
Figure 5.1: Sillimanite pseudomorphs after
andalusite (ZLDD5001-30.2m).
Figure 5.2: Curvilinear cleavages within
galena (ZLDD5001-216.1m).
Sph
Carb Qtz
Sph
400µm 400µm
Figure 5.3: Folding of carbonate vein through
sphalerite (ZLDD5001-137.9m).
Figure 5.4: Highly fractured quartz grain
within dominantly sphalerite matrix (Kintore
Lode Traverse 2-0.7m).
Qtz Carb
GarSph
550µm Py
Figure 5.5: Pyrite filling fractures in sphalerite
and remobilised within carbonate vein
(ZLDD5001-137.9m).
Figure 5.6: Euhedral garnet in association with
biotite and gahnite, forming a prograde
schistosity (ZLDD5002A-132.3m).
Bio400µm Gah
57
Chapter Five – Sulphide Rock Petrography
5.3.3 Remobilisation Features
Cpy
Figure 5.9: Inclusions of chalcopyrite and
pyrrhotite within sphalerite (Kintore Lode
Traverse 2-0m).
Figure 5.7: Exsolved chalcopyrite within
quartz crystals and in interstices between
quartz crystals (ZLDD5001-136.9m).
Qtz Cpy
Sph
Cpy
Po
550µm
550µm
Ga Qtz
400µmQtz
Figure 5.8: Exsolved chalcopyrite and folded
microfractures filled by chalcopyrite within
quartz (ZLDD5001-136.9m).
Qtz Ga
Apy
Figure 5.10: Euhedral arsenopyrite
overgrowing quartz and galena (Kintore Lode
Traverse 2-1.8m).
400µm
SphQtz
Ga 550µm 550µm
Figure 5.11: Galena filling fractures in
euhedral quartz grain (ZLDD5001-173.5m).
Figure 5.12: Galena and sphalerite occupying
space between quartz crystals and quartz
crystal fragments (Kintore Lode Traverse 2-
0m).
58
Chapter Five – Sulphide Rock Petrography
Qtz Ga
Figure XX:
550µm
Figure 5.13: Pyrrhotite occupying space
between quartz crystals with euhedral
arsenopyrite (ZLDD5001-173.5m)
550µmCpy Qtz
Figure 5.14: Curved boundary of chalcopyrite
(ZLDD5000-172.3m).
Apy Po
QtzGa
Cpy Sph
Po Cpy Apy
Sph550µm 550µm
Figure 5.15: Pyrrhotite vein crosscutting
chalcopyrite and sphalerite crystals
(ZLDD5001-214.6m).
Figure 5.16: Arsenopyrite partially rimmed by
chalcopyrite, hosted by sphalerite
(ZLDD5002A-132.3m).
Py Qtz Carb
Po 550µm 550µm
Figure 5.17: Pyrite remobilised within late
stage carbonate vein (ZLDD5001-137.9m).
Figure 5.18: Late stage fluid vein crosscutting
pyrrhotite crystal which is mobilised along the
vein (ZLDD5001-133.4m).
59
Chapter Five – Sulphide Rock Petrography
5.3.4 Retrogression and Alteration Features
Bio Sph
SphMu
Bio Gar
400µm 400µm
Figure 5.20: Partial replacement of sphalerite
with biotite, with later partial replacement of
biotite by muscovite (ZLDD5001-216.1m).
Figure 5.19: Sphalerite overgrowing biotite
(ZLDD5002A-132.3m).
Mu Bio
Carb
Sph Qtz 400µm 400µm
Figure 5.21: Retrograde muscovite alteration
of biotite after replacement by sphalerite
under crossed-polars (ZLDD5001-136.1).
Figure 5.22: Late stage carbonate vein within
quartz with sequential layers from the edge of
the vein to the centre (ZLDD5001-134m).
60
Chapter Five – Sulphide Rock Petrography
Figure 5.23: Replacement of biotite by gahnite
(ZLDD5001-214.6m).
Figure 5.24: Garnet rim around gahnite
(ZLDD2A-132.3m).
QtzGah Gah
Bio Gar
400µm 400µm
Qtz
Tet
Gud
Cpy
Apy
Ga
Qtz
400µm
Figure 5.25: Breakdown of tetrahedrite to gudmundite and chalcopyrite with
associated euhedral arsenopyrite, hosted by galena (ZLDD5001-216.1m).
5.4 Discussion It has been shown experimentally that sphalerite is more competent and less easily
deformed than other sulphides (Marshall and Gilligan, 1987) and this is observed in the
zinc lodes. It is inferred that sphalerite crystal growth occurred in two episodes, initially
during peak prograde metamorphism and later during post-peak prograde metamorphism.
Sphalerite grown during the second stage of growth is observed replacing prograde biotite
(Figure 5.19) while both prograde and retrograde sphalerite is observed being replaced by
retrograde biotite (Figure 5.20). After prograde growth, galena has undergone
remobilisation during high-grade metamorphic events, probably during M2/D2 and M3/D3,
61
Chapter Five – Sulphide Rock Petrography
where secondary galena fills fractures within deformed gangue minerals (Figures 5.11 and
5.12). In places, galena has been altered by chlorite and biotite during retrograde events.
Pyrrhotite and chalcopyrite have been remobilised in places (Figures 5.13, 5.14 and 5.15)
and also occur as inclusions within galena and sphalerite (Figures 5.7-5.9 and 5.16).
Recent studies have attempted to show that multiphase sulphide inclusions within gangue
minerals and low interfacial angles between sulphide minerals suggest the melting of the
Broken Hill orebody (Mavrogenes et al., 2001). Experiments have been conducted that
show the melting temperature for the experimental sulphide assemblages is lower than the
temperature reached during peak prograde metamorpism at Broken Hill. Results of the
experiments show that for the experimental assemblages, polymetallic melts form between
500-600oC, which is well under the temperatures identified relating to M1/M2. The results
show that the melt will initially become enriched in the low-melting point chalcophile
elements Ag, As, Au, Bi, Hg, Sb, Se, Sn, Tl and Te, upon further increased temperatures
will become enriched in Cu and Pb, and in the highest temperature conditions, will become
enriched in Fe, Mn, Zn, Si, H20 and F. These experiments however, used mineral
assemblages significantly different to those at Broken Hill, and therefore are not directly
comparable. Furthermore, there are no ores within the Broken Hill orebody that are
enriched in the low-melting point chalcophile elements. The findings do show that partial
melting is possible during metamorphism of sulphide bearing assemblages including
Broken Hill, but it is yet to be proven on assemblages found within the Broken Hill
orebody. Other studies suggest that polymetallic inclusions result from the crystallisation
of sulphides prior to low surface energy solid-state equilibration (Stanton, 1972).
The lack of any Ag-rich minerals after the breakdown of argentian tetrahedrite to
chalcopyrite and gudmundite (Figure 5.25) (Lawrence, 1968) suggests that there has been a
net loss of Ag from the system, therefore showing the orebdy metamorphism is not
isochemical. It has been suggested from sampling and drilling that the shear zones are
enriched with Ag. Therefore, it is possible there is a net movement of Ag from the B Lode,
A Lode, 1 Lens and Kintore Lode into shear zones during retrograde metamorphism, as has
been suggested by Plimer (1980) for the entire Broken Hill orebody.
Quartz is present in both prograde and retrograde rocks, and along with garnet and
gahnite is associated with the ore lodes. Quartz crystals were widely observed in the core
of altered gahnite and garnet crystals, and this suggests that the growth of prograde quartz
occurred before the growth of prograde gahnite and garnet, which provides support to there
being multiple prograde peak metamorphic events. The presence of garnet rims around
62
Chapter Five – Sulphide Rock Petrography
some gahnite grains (Figure 5.24) suggests multiple garnet growth phases, possibly
correlating with one period of prograde growth and a second period of growth during a
second prograde event or during a later retrograde event. Parr (1992b) suggested a
retrograde reaction rim between gahnite and retrograde Fe, Mn, Mg, Ca, Na and Si-rich
fluids. This feature was also observed in the C Lode on CML7 (Sproal, 2001). Alteration
of garnet, gahnite and sulphide minerals by biotite, chlorite and muscovite (Figures 5.20,
5.21 and 5.23), is inferred to correlate with the multiple retrograde events that have
occurred after peak metamorphism. Carbonate veins crosscut both gangue and sulphide
minerals (Figures 5.5, 5.17, 5.18 and 5.22) suggesting late stage fluid flow through the
rocks, resulting in the fracturing of the competent minerals and minor remobilisation of the
least competent minerals such as pyrrhotite and galena and formation of pyrite from
residual sulphur in the veins with iron liberated from the retrograde breakdown of
pyrrhotite. The sequentially layered veins suggest sequential precipitation of carbonate
minerals (Plimer, 1984) or a series of quick, episodic fluid flows.
63
Chapter Six – Sulphide Rock Mineral Chemistry
Chapter Six - Sulphide Rock Mineral Chemistry 6.1 Introduction From the 25 polished sections, ten were selected for further study with Electron
Microprobe Analysis (EMPA), using a Cameca SX-50 electron microprobe. Sections from
each zinc lode that show a wide variety of minerals or those that contained minerals with
unusual paragenetic relationships were chosen for the analysis. The sections were digitised
and coated with carbon before undergoing the microprobe analysis. EMPA is able to
determine the chemistry of a given point within a mineral or determine compositional
zoning within a single mineral. Galena and garnet were analysed with five-point traverses
from the centre of the mineral to the edge in order to determine compositional variability.
All elements present in greater than one atomic percent (A%) have been included in the
calculated formula, while all elements present in abundances between 0.10 and 0.99 A%
have been listed as trace elements.
6.2 Sulphide Minerals A total of 330 points were analysed on sulphide minerals, comprising 165 galena, 44
sphalerite, 41 pyrrhotite, 48 chalcopyrite, 10 arsenopyrite, 7 tetrahedrite, 8 gudmundite and
7 pyrite. These were analysed for S, Mn, Fe, Co, Ni, Cu, Zn, As, Ag, Cd, Sb, Pb, Bi and
some for Au. A current of 2.012nA and acceleration potential of 19.91kV were used. The
results were scrutinised for any inconsistent results, which may have arisen due to analysis
of minute inclusions, angled grain boundaries, grain pits or adhesive. The average atomic
abundances of all elements was calculated for each mineral in each ore lode. From these,
the average stoichiometric formula for each mineral was calculated for each ore lode, in
accordance with Deer et al. (1992) using empirical formulae from Strunz and Nickel
(2001).
Galena
165 analyses of galena were carried out as five-point traverses, from the centre of 33
galena grains to the edge of the grain in sections from the B Lode (5), A Lode (10), 1 Lens
(8) and Kintore Lode (10). The calculated average chemical formula for galena did not
vary significantly between the four analysed lodes (Table 6.2a), being close to the
stoichiometric formula of galena, PbS. Each showed a slight overfilling of the Pb site for a
corresponding underfilling of the S anion site. The abundance of Ag ranged from 0.033
64
Chapter Six – Sulphide Rock Mineral Chemistry
A% in B Lode and Kintore Lode, 0.038 A% in 1 Lens, to a maximum of 0.092 A% in A
Lode (Figure 6.1). In comparison to other studies on CML7, B Lode, Kintore Lode and 1
Lens showed relatively uniform Ag in galena, while A Lode and 3 Lens have anomalously
high Ag. Sb is present in similar abundances as Ag. Trace amounts of Zn were present in
trace abundances, higher in the B Lode and Kintore Lode and may have resulted from
analysis of minute Zn-bearing inclusions in galena or grain boundary diffraction of the
electron beam.
Table 6.2a: Average EMPA analysis for galena in B Lode, A Lode, 1 Lens and Kintore Lode.
Ore Lode Element
B Lode (n=31) A Lode (n=58) 1 Lens (n=46) Kintore Lode (n=50)A%(S) 48.707 48.488 48.490 48.386
A%(Mn) 0.023 0.032 0.028 0.022 A%(Fe) 0.032 0.039 0.038 0.014 A%(Co) 0.015 0.018 0.015 0.024 A%(Ni) 0.009 0.015 0.008 0.012 A%(Cu) 0.036 0.042 0.039 0.044 A%(Zn) 0.041 0.040 0.127 0.122 A%(As) 0.021 0.017 0.012 0.018 A%(Ag) 0.033 0.085 0.035 0.033 A%(Cd) 0.080 0.077 0.077 0.070 A%(Sb) 0.034 0.065 0.053 0.088 A%(Au) - 0.012 - 0.028 A%(Pb) 50.967 51.076 51.078 51.138 A%(Bi) 0.001 0.001 0.001 0.001
TOTAL A% 100.000 100.000 100.000 100.000 Calculated
Formula Pb1.023S0.975 Pb1.027S0.970 Pb1.027S0.97 Pb1.029S0.968
Average Ag in galena
0.000
0.020
0.040
0.060
0.080
0.100
KintoreLode
(n=50)
B Lode(n=25)
A Lode(n=50)
1 Lens(n=40)
WesternMin.
2 Lens 3 Lens
Ore Lode
Ag (A
%)
Figure 6.1: Average
abundance of Ag in
galena at Broken Hill
(Western Min. data
from Kitchen, 2001; 2
Lens and 3 Lens data
from Both, 1973).
65
Chapter Six – Sulphide Rock Mineral Chemistry
Traverses across galena grains show that Pb (Figure 6.2) is relatively uniform
across grains from B Lode, 1 Lens and Kintore Lode. A Lode shows a slight increase in Pb
from the first traverse point to the fourth traverse point. A feature commonly observed in
the B Lode, A Lode and 1 Lens is the distinct decrease in Pb at the very edge of the galena
crystal. A feature commonly observed in all the ore lodes except the Kintore Lode is the
distinct decrease in lead at the very edge of the galena crystal. Ag was highly variable
(Figure 6.3) from one point to the next along individual traverses and in comparison to
other traverses.
Kintore Lode galena traverse Pb abundance
47
48
49
50
51
52
53
1 2 3 4 5
Traverse point
Pb
(A%
)
B Lode galena traverse Pb abundance
49.6
50
50.4
50.8
51.2
51.6
52
1 2 3 4 5
Traverse point
Pb
(A%
)
A Lode galena traverse Pb abundance
47
48
49
50
51
52
53
1 2 3 4 5
Traverse point
Pb (A
%)
1 Lens galena traverses Pb abundance
49.5
50
50.5
51
51.5
52
1 2 3 4 5
Traverse point
Pb (A
%)
Figure 6.2: Compositional variation of Pb across galena grains.
66
Chapter Six – Sulphide Rock Mineral Chemistry
Kintore Lode galena traverse Ag abundance
0
0.04
0.08
0.12
0.16
0.2
1 2 3 4 5
Traverse point
Ag
(A%
)
B Lode galena traverse Ag abundance
0
0.05
0.1
0.15
0.2
0.25
1 2 3 4 5
Traverse point
Ag (A
%)
A Lode galena traverse Ag abundance
0
0.04
0.08
0.12
0.16
0.2
1 2 3 4 5
Traverse point
Ag (A
%)
Kintore Lode galena traverse Ag abundance
0
0.04
0.08
0.12
0.16
0.2
1 2 3 4
Traverse point
Ag
(A%
5)
Figure 6.3: Compositional variation of Ag across galena grains.
Sphalerite
44 analyses of sphalerite were carried out on sections from the B Lode (15), A Lode (11), 1
Lens (8) and Kintore Lode (10). Sphalerite has the stoichiometric formula of ZnS, however
the analyses show (Table 6.2b) that sphalerite has compositional differences between the
ore lodes. The calculated formula is variable with a significant amount of Fe substituting
for Zn in all ore lodes.
B Lode shows the highest deviance from the stoichiometric formula for sphalerite
as a result of Fe substitution (Figure 6.4), and produced a calculated formula of (Zn0.798,
Fe0.198)S0.999. The Kintore Lode (0.336 A%) contained the highest abundance of Mn
present as a trace element, with B Lode (0.179 A%) also having Mn present as a trace
element (Figure 6.5). A Lode (0.155 A%), 1 Lens (0.390 A%) and Kintore Lode (0.144
A%) show slight enrichment in Cd, which is present as a trace element (Figure 6.6).
Sphalerite contains low Ag, ranging from 0.009 A% (B Lode) to 0.028 A% (A Lode).
67
Chapter Six – Sulphide Rock Mineral Chemistry
Table 6.2b: Average EMPA analysis for sphalerite in B Lode, A Lode, 1 Lens and Kintore Lode. Ore Lode
Element B Lode (n=15) A Lode (n=11) 1 Lens (n=8) Kintore Lode
(n=10) A%(S) 49.990 49.714 49.824 49.892
A%(Mn) 0.179 0.061 0.025 0.336 A%(Fe) 9.800 8.383 8.304 7.660 A%(Co) 0.009 0.027 0.034 0.005 A%(Ni) 0.008 0.005 0.010 0.009 A%(Cu) 0.014 0.013 0.081 0.011 A%(Zn) 39.862 41.555 41.231 41.880 A%(As) 0.024 0.025 0.035 0.036 A%(Ag) 0.009 0.028 0.014 0.007 A%(Cd) 0.086 0.155 0.390 0.114 A%(Sb) 0.004 0.003 0.002 0.002 A%(Au) 0.000 - - 0.000 A%(Pb) 0.003 0.003 0.003 0.002 A%(Bi) 0.013 0.028 0.047 0.045
TOTAL A% 100.000 100.000 100.000 100.000 Calculated
Formula (Zn0.798, Fe0.198)S0.999 (Zn0.834, Fe0.168)S0.994 (Zn0.834, Fe0.166)S0.996 (Zn0.834, Fe0.153)S0.998
Zn vs Fe in sphalerite
0
2
4
6
8
10
12
38 39 40 41 42 43
Zn (A%)
Fe (A
%)
Kintore B Lode A Lode 1 Lens
Figure 6.4: Inter-element plot of Zn
and Fe in sphalerite, with B Lode
having the highest amount of
substitution of Fe for Zn, followed
by equivalent amounts in A Lode,
Kintore Lode and 1 Lens.
Zn vs Mn in sphalerite
00.05
0.10.15
0.20.25
0.30.35
0.40.45
38 39 40 41 42 43
Zn (A%)
Mn
(A%
)
Kintore B Lode A Lode 1 Lens
Figure 6.5: Inter-element plot of Zn
and Mn in sphalerite, with the
Kintore Lode a showing a greater
enrichment in Mn than B Lode with
low abundances in A Lode and 1
Lens.
68
Chapter Six – Sulphide Rock Mineral Chemistry
Zn vs Cd in sphalerite
00.10.20.30.40.50.60.70.80.9
38 39 40 41 42 43
Zn (A%)
Cd
(A%
)
Kintore B Lode A Lode 1 Lens
Pyrrhotite
41 analyses of pyrrhotite were carried out on sections from B Lode (16), A Lode (15), 1
Lens (5) and Kintore Lode (5)(Table 6.2c). Pyrrhotite has the stoichiometric formula Fe1-
xS. Across all zinc lodes, pyrrhotite commonly was underfilled in the cation site and
overfilled in the anion site, typical for pyrrhotite (Struntz and Nickel, 2001). Zinc was
present in trace abundances within the B Lode and Kintore Lode. Ag is negliable in
pyrrhotite, ranging from 0.003 A% (1 Lens) to 0.008 (Kintore Lode).
Table 6.2c: Average EMPA analysis for pyrrhotite in B Lode, A Lode, 1 Lens and Kintore Lode.
Ore Lode Element
B Lode (n=16) A Lode (n=15) 1 Lens (n=5) Kintore Lode (n=5)
A%(S) 51.928 52.412 52.120 51.368 A%(Mn) 0.007 0.005 0.001 0.015 A%(Fe) 47.616 47.389 47.600 47.896 A%(Co) 0.005 0.025 0.045 0.008 A%(Ni) 0.009 0.020 0.018 0.004 A%(Cu) 0.011 0.008 0.002 0.020 A%(Zn) 0.288 0.011 0.079 0.550 A%(As) 0.087 0.085 0.096 0.100 A%(Ag) 0.007 0.006 0.003 0.008 A%(Cd) 0.004 0.009 0.026 0.005 A%(Sb) 0.004 0.007 0.003 0.001 A%(Au) - - - 0.000 A%(Pb) 0.003 0.005 0.003 0.000 A%(Bi) 0.022 0.018 0.005 0.024
TOTAL A% 99.992 100.000 100.000 100.000 Calculated
Formula Fe0.952S1.039 Fe0.948S1.048 Fe0.952S1.042 Fe0.958S1.027
Figure 6.6: Inter-element plot of Zn
and Cd in sphalerite, with 1 Lens
having a significantly higher
abundance of Cd than the B Lode, A
Lode and Kintore Lode.
69
Chapter Six – Sulphide Rock Mineral Chemistry
Pyrrhotite has two structural polymorphs, hexagonal pyrrhotite forms during high-
grade metamorphism, whereas monoclinic pyrrhotite forms by the retrogression of
hexagonal pyrrhotite. The atomic abundance of Fe in pyrrhotite varied from between
47.389 (A Lode) and 47.896 A% (Kintore Lode). This indicates that there is both
hexagonal and monoclinic forms of pyrrhotite present in the ore zone assemblages (Scott et
al., 1977).
Chalcopyrite
48 analyses of chalcopyrite were carried out on sections from the B Lode (15), A Lode
(13), 1 Lens (10) and Kintore Lode (10)(Table 6.2d). Chalcopyrite in the zinc lodes is close
to stoichiometric, with a slight overfilling of Fe in relation to Cu and S. The Kintore Lode
shows a trace abundance of Zn. Ag is present in an anomalously high abundance in A Lode
chalcopyrite (0.070 A%)(Figure 6.6) and in low amounts in the other ore lodes (Figure
6.7), ranging from 0.005 (Kintore Lode) to 0.020 A% (1 Lens), where it substitutes for Cu.
As is present in uniform abundances across the ore lodes, while Sb and Cd are relatively
low.
Table 6.2d: Average EMPA analysis for chalcopyrite in B Lode, A Lode, 1 Lens and Kintore Lode.
Ore Lode Element
B Lode (n=10) A Lode (n=18) 1 Lens (n=10) Kintore Lode (n=10)
A%(S) 49.630 49.554 49.611 49.582 A%(Mn) 0.006 0.024 0.007 0.016 A%(Fe) 25.625 25.410 25.491 25.405 A%(Co) 0.007 0.003 0.009 0.003 A%(Ni) 0.007 0.007 0.004 0.005 A%(Cu) 24.538 24.749 24.738 24.706 A%(Zn) 0.096 0.087 0.044 0.150 A%(As) 0.053 0.052 0.043 0.043 A%(Ag) 0.019 0.070 0.020 0.005 A%(Cd) 0.005 0.010 0.005 0.016 A%(Sb) 0.003 0.003 0.004 0.003 A%(Au) 0.012 - - 0.020 A%(Pb) 0.000 0.004 0.003 0.004 A%(Bi) 0.006 0.027 0.020 0.044
TOTAL A% 100.000 100.000 100.000 100.000 Calculated
Formula Cu0.985Fe1.0327S1.988 Cu0.995Fe1.022S1.983 Cu0.991Fe1.022S1.986 Cu0.991Fe1.024S1.985
70
Chapter Six – Sulphide Rock Mineral Chemistry
Average Ag in chalcopyrite
0.000
0.020
0.040
0.060
0.080
KintoreLode(n=10)
B Lode(n=10)
A Lode(n=18)
1 Lens(n=10)
WesternMin.
C Lode 2 Lens
Ore Lode
Ag
(A%
)
Arsenopyrite
10 analyses of arsenopyrite were carried out on sections from the A Lode (5) and Kintore
Lode (5)(Table 6.2e). In both lodes, arsenopyrite contains excess As, deficient S and
deficient Fe as a result of Co substitution. The Kintore Lode shows a widespread linear
trend of Co relative to Fe, whereas A Lode shows a closely grouped linear Fe:Co trend
(Figure 6.8).
Table 6.2e: Average EMPA analysis for arsenopyrite in A Lode and Kintore Lode.
Ore Lode Element
A Lode (n=5) Kintore lode (n=5)
A%(S) 31.391 29.190 A%(Mn) 0.046 0.017 A%(Fe) 31.889 29.305 A%(Co) 1.016 2.938 A%(Ni) 0.009 0.883 A%(Cu) 0.009 0.005 A%(Zn) 0.016 0.005 A%(As) 35.572 37.612 A%(Ag) 0.006 0.005 A%(Cd) 0.008 0.005 A%(Sb) 0.023 0.032 A%(Au) - 0.000 A%(Pb) 0.016 0.003 A%(Bi) 0.000 0.000
TOTAL A% 100.000 100.000 Calculated
Formula (Fe0.956, Co0.030)As1.068S0.942 (Fe0.879, Co0.088)As1.129S0.876
Figure 6.7: Average
abundance of Ag in
chalcopyrite on CML7
(Western Min. data
from Kitchen, 2001; C
Lode and 2 Lens data
from Sproal, 2001).
71
Chapter Six – Sulphide Rock Mineral Chemistry
Fe vs Co in arsenopyrite
0.0000.5001.0001.5002.0002.5003.0003.5004.0004.500
27.000 28.000 29.000 30.000 31.000 32.000 33.000
Fe (A%)
Co
(A%
)
Kintore Lode A Lode
Figure 6.8: Inter-element plot for
Fe and Co in arsenopyrite from
the Kintore Lode and A Lode,
showing the linear trend related to
the substitution of Co for Fe.
Pyrite
A total of seven grains of pyrite were analysed from within microfractures in sections cut
from B Lode (Table 6.2f). The calculated formula was Fe1.036S1.960.
Table 6.2f: Average EMPA analysis for pyrite in B Lode.
Element B Lode (n=7)
A%(S) 65.314 A%(Mn) 0.006 A%(Fe) 34.488 A%(Co) 0.011 A%(Ni) 0.029 A%(Cu) 0.007 A%(Zn) 0.012 A%(As) 0.073 A%(Ag) 0.005 A%(Cd) 0.002 A%(Sb) 0.034 A%(Au) 0.002 A%(Pb) 0.000 A%(Bi) 0.014
TOTAL A% 100.000
Calculated Formula Fe1.036S1.960
Tetrahedrite
A total of seven analyses of tetrahedrite were carried out on sections from the 1 Lens
(Table 6.2g). The calculated formula for tetrahedrite was (Cu8.150Ag1.700Fe1.505Zn0.495)
Sb4.435S12.693.
72
Chapter Six – Sulphide Rock Mineral Chemistry
Tetrahedrite is a prograde sulphide, which at Broken Hill is argentian tetrahedrite
(freibergite). Tetrahedrite is a complex mineral with variable substitutions. Tetrahedrite is
the primary Ag-bearing mineral at Broken Hill. The samples from 1 Lens reflect the high
Ag contained in tetrahedrite, with an average of 5.861 A% Ag contained within the seven
analysed samples of tetrahedrite, although is considerably lower than observed in the
Western Mineralisation by Kitchen (2001)(Figure 6.9). Fe and Zn, along with Ag are
present in significant abundances, substituting for Cu. Both the Sb and S sites are
overfilled.
Table 6.2g: Average EMPA analysis for tetrahedrite in 1 Lens.
Element 1 Lens (n=7)
A%(S) 43.768 A%(Mn) 0.008 A%(Fe) 5.190 A%(Co) 0.014 A%(Ni) 0.005 A%(Cu) 28.104 A%(Zn) 1.708 A%(As) 0.929 A%(Ag) 5.861 A%(Cd) 0.026 A%(Sb) 14.365 A%(Pb) 0.006 A%(Bi) 0.016
TOTAL A% 100.000
Calculated Formula (Cu8.150Ag1.700Fe1.505Zn0.495)Sb4.435S12.693
Average Ag in tetrahedrite
0.000
2.000
4.000
6.000
8.000
10.000
12.000
14.000
16.000
1 Lens (n=7) 2 Lens Western Min.
Ore Lode
Ag
(A%
)
Figure 6.9: Average
abundance of Ag in
tetrahedrite on
CML7 (Western Min.
data from Kitchen,
2001; 2 Lens data
from Sproal, 2001).
73
Chapter Six – Sulphide Rock Mineral Chemistry
It has been suggested in the literature that tetrahedrite breaks down during
retrograde metamorphism to a silver-rich secondary mineral and a silver-poor secondary
mineral (Lawrence, 1968). The silver-poor minerals are commonly gudmundite,
chalcopyrite, arsenopyrite and lÖllingite. The silver-rich minerals were not observed in this
study consist of pyrargyrite, polybasite, stephenite and argentite.
Gudmundite
Eight grains of gudmundite were analysed, including grains from 1 Lens (5) in association
with tetrahedrite and chalcopyrite and B Lode (3) in association with galena and
chalcopyrite (Table 6.2h). Gudmundite has the empirical formula of FeSbS however, in the
Broken Hill orebody, it has a complex chemistry related to its complex formation history.
The average formula for gudmundite in the B Lode was (Fe0.900Co0.045)(Sb1.038As0.066)S0.932
whereas in the 1 Lens was (Fe0.949)(Sb1.033As0.069)S0.939. Along with the major substitutions
of Co and As, there were a number of trace elements recorded, including Ni, Cu, Zn, Bi
and Ag. The abundance of this wide range of trace elements was highly variable within
each ore lode suggesting no dominant substitution patterns.
Table 6.2h: Average EMPA analysis for gudmundite in B Lode and 1 Lens.
Ore Lode Element
B Lode (n=3) 1 Lens (n=5)
A%(S) 31.074 31.297 A%(Mn) 0.004 0.005 A%(Fe) 30.015 31.632 A%(Co) 1.487 0.015 A%(Ni) 0.193 0.049 A%(Cu) 0.233 0.144 A%(Zn) 0.059 0.062 A%(As) 2.210 2.313 A%(Ag) 0.029 0.015 A%(Cd) 0.001 0.001 A%(Sb) 34.612 34.438 A%(Pb) 0.001 0.011 A%(Bi) 0.082 0.018
TOTAL A% 100.000 100.000
Calculated Formula (Fe0.900Co0.045)(Sb1.038As0.066)S0.932 (Fe0.949)(Sb1.033As0.069)S0.939
74
Chapter Six – Sulphide Rock Mineral Chemistry
6.3 Gangue Minerals A total of 281 points on gangue minerals were analysed including 225 garnets, 15 gahnite,
33 biotite, 15 muscovite, 4 chlorite and 4 of carbonate minerals. These were analysed for
Si, Ti, Al, Fe, Cr, V, Mn, Ca, Mg, Zn, Na and K. An emission current of 2.514nA and
acceleration potential of 14.94kV were used. The results were scrutinised for any
inconsistent results that may have arisen due to analysis of inclusions, angled grain
boundaries, grain pits or adhesive. The average atomic abundances of all elements were
calculated for each gangue mineral in each ore lode. From these, the average
stoichiometric formula of each gangue mineral was calculated for each ore lode, in
accordance with Deer et al. (1992) using empirical formulae from Strunz and Nickel
(2001).
Garnet
A total of 225 electron microprobe analyses of garnet were completed (Table 6.3a) and the
end members were calculated (Table 6.3b) and contrasted with garnets from ore lodes on
CML7 (Figure 6.10). This derived from the traversing of 45 individual garnet grains with
five-point traverses.
Table 6.3a: Average EMPA analysis for garnet in B Lode, A Lode, 1 Lens and Kintore Lode.
Ore Lode Element B Lode (n=50) A Lode (n=75) 1 Lens (n=50) Kintore Lode (n=50)
Si 3.007 2.955 2.964 2.988 Ti 0.002 0.002 0.001 0.004
Al/Al IV 0.004 0.045 0.036 0.014 Al VI 1.955 1.951 1.925 1.942 Cr 0.002 0.001 0.001 0.002
Fe3+ 0.020 0.081 0.103 0.051 Fe2+ 1.445 1.833 2.200 0.905
V 0.014 0.011 0.007 0.008 Mn2+ 1.021 0.620 0.354 1.322 Mg 0.213 0.263 0.363 0.155 Zn 0.003 0.003 0.004 0.004 Ni 0.000 0.000 0.000 0.000 K 0.000 0.000 0.001 0.000 Na 0.003 0.003 0.002 0.001 Ca 0.305 0.232 0.040 0.601 Nb 0.000 0.000 0.000 0.000
Sum 7.995 8.000 8.000 8.000
75
Chapter Six – Sulphide Rock Mineral Chemistry
Table 6.3b: Garnet end member abundances determined from recalculation of EMPA garnet
compositions.
Garnet B Lode (n=50) A Lode (n=75) 1 Lens (n=50) Kintore Lode (n=50)
Pyrope Mg3Al2(SiO4)3
7.131 8.912 12.281 5.215
Almandine Fe3Al2(SiO4)3
48.409 62.195 74.403 30.315
Spessartine Mn3Al2(SiO4)3
34.225 21.024 11.971 44.323
Andradite Ca3Fe2
3+(SiO4)3
0.986 3.298 1.242 2.541
Uvarovite Ca3Cr2(SiO4)3
0.082 0.051 0.059 0.083
Grossular Ca3Al2(SiO4)3
9.168 4.530 0.059 17.523
TOTAL 100.000 100.010 100.015 100.000
Average total ore lode garnet compositions
01020304050607080
B Lode(n=50)
A Lode(n=75)
KintoreLode(n=50)
1 Lens(n=50)
WesternMin.
C Lode 2 Lens
Ore Lode
Abu
ndan
ce (A
%)
PyropeAlmandineSpessartineAndraditeUvaroviteGrossular
Figure 6.10: Average modal abundance of garnet endmembers in each CML7 ore lode, including B
Lode, A Lode, Kintore Lode and 1 Lens (this study), the Western Mineralisation (Kitchen, 2001)
and C Lode and 2 Lens (Sproal, 2001).
From the atomic abundance of the garnets, individual end members were calculated
on the basis of 12 O. These are shown in Table 6.3.2 and Figure 6.3.1. B Lode and the
Kintore Lode consist of dominant almandine, over spessartine and minor pyrope. A Lode,
1 Lens, Western Mineralisation and C Lode are dominantly almandine with minor
76
Chapter Six – Sulphide Rock Mineral Chemistry
spessartine and pyrope. 2 Lens contains anomalously high grossular garnet, with
spessartine and almandine also co-dominant.
Each garnet was analysed with a traverse of five points from the centre of the grain
to the periphery and these were calculated to give the average abundance across a garnet
grain in each ore lode (Figure 6.11). The B Lode shows a strong increase in almandine
garnet on the rim for a corresponding decrease in both spessartine and grossular garnet.
The A Lode and 1 Lens show a slight increase in almandine for a slight decrease in
spessartine and grossular, while the Kintore Lode garnets show a decrease in spessartine,
andradite and pyrope for an increase in almandine and grossular garnet. This shows that for
B Lode, A Lode and 1 Lens, a loss of Mn and Ca and a gain of Fe occurred. The Kintore
Lode traverse data suggests a loss of Mg and Mn and a reworking of Ca and Fe in
andradite to grossular and almandine garnet.
B Lode average traverse point garnet composition
0
10
20
30
40
50
60
1 2 3 4 5
Traverse Point
Abu
ndan
ce (%
) PyropeAlmandineSpessartineAndraditeUvaroviteGrossular
1 Lens average traverse point garnet composition
0
10
20
30
40
50
60
70
80
1 2 3 4 5
Traverse Point
Abu
ndan
ce (%
) PyropeAlmandineSpessartineAndraditeUvaroviteGrossular
A Lode average traverse point garnet composition
0
10
20
30
40
50
60
70
1 2 3 4 5
Traverse Point
Abu
ndan
ce (%
) PyropeAlmandineSpessartineAndraditeUvaroviteGrossular
Kintore Lode average traverse point garnet composition
05
101520253035404550
1 2 3 4 5
Traverse Point
Abu
ndan
ce (%
) PyropeAlmandineSpessartineAndraditeUvaroviteGrossular
Figure 6.11: Average garnet composition from core to rim for each ore lode.
Spinel
A total of 15 spinels were analysed, 10 from A Lode and 5 from 1 Lens (Table 6.3c). The
average stoichiometric formula determined from those analyses is (Zn0.6757 Fe0.2686 Mg0.0585
Mn0.0027V0.0092)(Al1.9836)O4 for A Lode and (Zn0.6944 Fe0.231 Mg0.062)(Al2.0046)O4 for 1 Lens.
77
Chapter Six – Sulphide Rock Mineral Chemistry
The zinc spinel gahnite was the dominant variety (Table 6.3d), followed by lower
abundances of hercynite and Mg-spinel. Trace amounts of galaxite were present in both
lodes. A vanadium rich variety was present in trace amounts in the A Lode, possibly
magnesiocoulsonite (MgV2O4), coulsonite (FeV2O4) or vuorelainenite (MnV2O4) (Strunz
and Nickel, 2001). Although gahnite is the dominant spinel in all ore lodes, spinel from the
Western Mineralisation and C Lode on CML7 (Figure 6.12) contain slightly higher
gahnite, compared to the A Lode and 1 Lens, and the Pinnacles Mine, which contain
slightly more hercynite.
Table 6.3c: Average EMPA analysis for gahnite in A Lode and 1 Lens.
A Lode (n=10) 1 Lens (n=5) Ion
Average A% Standard Dev. Average A% Standard Dev. Si 0.000 0.001 0.000 0.000 Ti 0.000 0.001 0.000 0.000
Al/Al IV 0.000 0.000 0.000 0.000 Al VI 1.922 0.007 1.940 0.007 Cr 0.000 0.001 0.001 0.001
Fe3+ 0.128 0.010 0.119 0.007 Fe2+ 0.141 0.042 0.112 0.029
V 0.009 0.010 0.004 0.005 Mn2+ 0.003 0.001 0.003 0.001 Mg 0.059 0.011 0.062 0.003 Zn 0.676 0.040 0.694 0.024 Ni 0.000 0.000 0.000 0.000 K 0.000 0.000 0.000 0.000 Na 0.061 0.005 0.064 0.004 Ca 0.000 0.000 0.000 0.000 Nb 0.000 0.000 0.000 0.000
Sum Cat# 3.000 0.000 3.000 0.000
Table 6.3d: Gahnite end member abundances determined from recalculation of EMPA spinel
compositions.
A Lode (n=10) 1 Lens (n=5) Spinel Variety Mineral Formula Abundance A% Abundance A%
Gahnite (Zn) ZnAl2O4 66.59 70.14 Hercynite (Fe) FeAl2O4 26.47 23.33 Mg-spinel (Mg) MgAl2O4 5.77 6.26
V-spinel (Mg, Fe, Mn)V2O4 0.9 - Galaxite (Mn) MnAl2O4 0.27 0.26
78
Chapter Six – Sulphide Rock Mineral Chemistry
Figure 6.12: Average spinel endmember
abundances from A Lode and 1 Lens (this
study), Western Mineralisation (Kitchen,
2001), C Lode (Sproal, 2001) on CML7 and
at the Pinnacles Mine (Parr, 1992b).
Biotite
Table 6.3e: Average EMPA analysis for biotite in B Lode, A Lode, 1 Lens and Kintore Lode.
Ore Lode Element
B Lode (n=5) A Lode (n=15) 1 Lens (n=10) Kintore Lode (n=3)
Si 5.645 5.444 5.489 5.600
Ti 0.180 0.193 0.147 0.203
Al/Al IV 2.355 2.556 2.511 2.400
Al VI 0.408 0.565 0.571 0.288
Fe2+ 1.903 2.785 2.500 2.309
Mn2+ 0.037 0.022 0.013 0.064
Mg 3.202 2.274 2.658 2.991
Zn 0.018 0.014 0.014 0.024
K 1.815 1.758 1.708 1.861
Na 0.043 0.058 0.084 0.014
Ca 0.000 0.002 0.002 0.002
Nb 0.000 0.000 0.000 0.000
OH 4.000 4.000 4.000 4.000
Sum 15.684 15.697 15.711 15.779
79
Chapter Six – Sulphide Rock Mineral Chemistry
Table 2.3f: Calculated formula for biotite, determined from the recalculation of EMPA biotite analyses
data.
Ore Lode Formula
B Lode (n=5) (K1.815Na0.043)(Mg3.202Fe2+1.903)(Al0.408Ti0.180)[Si5.645Al2.355O20] (OH,F)4
A Lode (n=15) (K1.708Na0.014)(Mg2.991Fe2+2.785)(Al0.565Ti0.193)[Si5.444Al2.556O20] (OH,F)4
1 Lens (n=10) (K1.708Na0.084)(Mg2.658Fe2+2.500)(Al0.571Ti0.147)[Si5.489Al2.511O20] (OH,F)4
Kintore Lode (n=3) (K1.861Na0.014)(Mg2.991Fe2+
2.309)(Al0.288Ti0.203)[Si5.600Al2.400O20] (OH,F)4
33 analyses of biotite were completed from the B Lode (5), A Lode (15), 1 Lens (10) and
Kintore Lode (3) (Table 6.3e), and the chemical formula of biotite in each lode calculated
(Table 2.3f). Biotite can be classed as peraluminous varieties of the phlogopite-annite
series.
Figure 6.13: Plot of biotite
variety from various ore lodes
on CML7.
80
Chapter Six – Sulphide Rock Mineral Chemistry
Muscovite
15 samples of muscovite were analysed from B Lode (5), A Lode (7) and 1 Lens (3)(Table
6.3g) and the chemical formula was calculated for the muscovite in each ore lode (Table
6.3h).
Table 6.3g: Average EMPA analysis for muscovite in B Lode, A Lode and 1 Lens.
Ore Lode
Element B Lode (n=5) A Lode (n=7) 1 Lens (n=3)
Si 6.219 6.164 6.663
Ti 0.022 0.019 0.005
Al/Al IV 0.066 0.122 0.000
Al VI 5.421 5.469 4.633
Cr 0.003 0.002 0.003
Fe2+ 0.128 0.160 0.439
Mn2+ 0.003 0.005 0.003
Mg 0.171 0.154 0.309
Ca 0.003 0.004 0.003
Na 0.156 0.133 0.081
K 1.768 1.700 1.805
Zn 0.013 0.007 0.013
Ni 0.000 0.000 0.000
OH 12.571 12.571 12.571
Sum 13.975 13.937 13.957
Table 6.3h: Calculated formula for muscovite, determined from the recalculation of muscovite EMPA
data.
Ore Lode Formula
B Lode (n=5) (K1.768Na0.156)(Al5.421Fe0.128Mg0.171Zn0.013)[Si6.164Al0.066O20](OH,F)4
A Lode (n=7) (K1.700Na0.156)(Al5.469Fe0.160Mg0.154Zn0.007)[Si6.164Al0.122O20](OH,F)4
1 Lens (n=3) (K1.805Na0.081)(Al4.633Fe0.439Mg0.309Zn0.013)[Si6.663Al0.000O20](OH,F)4
The B Lode and A Lode are relatively enriched in Al and Na, while being depleted
in Fe and Mg, whereas the 1 Lens is comparatively Al poor, but rich in Fe and Mg. Mica
81
Chapter Six – Sulphide Rock Mineral Chemistry
from the zinc lodes plots in the aluminous phengite field, classified by Guidotti
(1984)(Figure 6.14) compared to C Lode and Western Mineralisation mica which plot in
the muscovite phase and 2 Lens which plots in between ferrimuscovite, muscovite,
phengite and ferriphengite.
Mu
Ph
Figure 6.14: Composition of
white mica from ore lodes on
CML7. Mu=muscovite,
Ph=phengite (divisions from
Guidotti 1984).
Chlorite
Chlorite was a rare mineral in the zinc lodes and, as a result, was only analysed in the A
Lode (1) and 1 lens (3)(Table 6.3i). The analyses were calculated for 36 ions based on 20
O and 16 (OH)(Table 6.3j). The analyses show that the composition of chlorite between
the A Lode and 1 Lens is markedly different compositionally, with A Lode chlorites being
Fe-rich and Mg-poor, whereas the 1 Lens is Mg-rich and Fe-poor. Chlorite in these ore
lodes plot within the ripidolite phase (Figure 6.15)(Hey, 1954).
82
Chapter Six – Sulphide Rock Mineral Chemistry
Table 6.3i: Average EMPA analysis for chlorite in A Lode and 1 Lens.
Ore Lode Element A Lode 1 Lens 1 Lens 1 Lens
Si 5.346 5.185 5.029 5.191 Ti 0.002 0.016 0.013 0.009
Al/Al IV 2.654 2.815 2.971 2.809 Al VI 2.924 2.673 2.799 2.715 Cr 0.012 0 0.002 0.003
Fe2+ 6.516 4.64 4.657 4.59 Mn2+ 0.024 0.024 0.032 0.03 Mg 2.329 4.655 4.533 4.646 Ca 0 0 0.004 0.001 Na 0.007 0.003 0.004 0.009 K 0.007 0.001 0.003 0.002
ZnO 0.044 0.045 0.029 0.039 Ni - - - - OH 16 16 16 16
Sum 19.865 20.057 20.076 20.044
Table 6.3j: Calculated formula for chlorite, determined from the recalculation of chlorite EMPA data.
Ore Lode Formula
A Lode (n=1) (Fe6.516Al2.924Mg2.329)(Si5.346Al2.654)O20(OH)16
1 Lens (n=3) (Fe4.629Al2.729Mg4.6113)(Si5.135Al2.865)O20(OH)16
Chlorite varieties in the A Lode and 1 Lens
00.10.20.30.40.50.60.70.8
5.000 5.100 5.200 5.300 5.400 5.500 5.600
Si (A%)
Fe/F
e+M
g
A Lode (n=1)1 Lens (n=3)
Ripidolite
Figure 6.15: Chlorite varieties in the A Lode and 1 Lens.
83
Chapter Six – Sulphide Rock Mineral Chemistry
Carbonates
The late stage propagation of veins through the Broken Hill ore lodes has been
documented in the literature by a number of authors (Lawrence, 1968; Plimer, 1984).
These veins have a wide variety of mineralogy and varied stable isotope values as observed
in Chapter 4, suggesting a number of generations of veining containing different fluid
chemistry. Four carbonate minerals were analysed by EMPA (Table 2.3k). Recalculation
of the EMPA data, shows that the primary constituent of the B Lode veins sampled is
siderite, with minor calcite and magnesite.
Table 6.3k: Average EMPA of carbonate minerals in B Lode.
Ore Lode Element B Lode B Lode B Lode B Lode
Si 0 0 0 0 Fe2+ 0.931 0.869 0.85 0.855 Mn2+ 0.014 0.007 0.005 0.009 Mg 0.03 0.054 0.056 0.061 Ca 0.023 0.07 0.088 0.074 Ba - - - - Sr - - - - Na 0.001 0 0.001 0 K 0 0 0 0 Pb - - - - Zn 0 0.002 0 0 Ni - - - - Co - - - - Cd - - - - Cu - - - -
Sum Cat# 1.001 1.002 1 1
Table 6.3l: Calculated formula for carbonate minerals, determined from the recalculation of carbonate
EMPA data. Carbonate Variety Mineral Formula Abundance %
Siderite Fe(CO3) 87.62
Calcite Ca(CO3) 6.34
Magnesite Mg(CO3) 5.04
Rhodochrosite Mn(CO3) 0.86
Eitelite Na2Mg(CO3)2 0.06
Smithsonite Zn(CO3) 0.05
Buetschildite K2Ca(CO3)2 0.01
TOTAL - 99.99
84
Chapter Six – Sulphide Rock Mineral Chemistry
6.4 Discussion
At Broken Hill, Ag is associated with tetrahedrite and galena (Lawrence, 1968; Both,
1973; Plimer, 1980). A number of other rare retrograde Ag-rich phases have been
identified including pyrargyrite, polybasite, stephanite, argentite, native silver, dyscrasite
and allargentum (Lawrence, 1968). Previous studies have shown that tetrahedrite is rare
within the zinc lodes (Both and Stumpfl, 1987), and is supported by this study, where
tetrahedrite is only present in 1 Lens.
This study has shown that on CML7, the low-grade vein style intersections of A
Lode and 1 Lens, although not containing high Ag in bulk rock composition, contains
relatively enriched abundances Ag within galena and chalcopyrite phases compared to
those of the B Lode and Kintore Lode. This suggests that Ag moves preferentially into
galena and chalcopyrite during the metamorphism and remobilisation of sulphides in veins.
The low bulk composition abundance of Ag in the A Lode and 1 Lens may represent an
initial low abundance of Ag in the rock prior to mobilisation or reflects an abundance that
is commensurate with the loss of Ag from the system, possibly into shear zones during
retrogression, as has been documented in previous studies (Plimer, 1980, 1987). The
Kintore Lode contained relatively low Ag content in all sulphides analysed by EMPA, yet
was shown to have an anomalous Ag content (169.6 g/t). This suggests that Ag was
contained within phases not observed and not analysed in this study, and provides an area
for further research. The inconsistency of Ag within galena across the grains, suggests that
Ag can be forced randomly into the galena lattice during deformation and metamorphism.
However it has been shown experimentally that the amount of Ag within galena is
constrained thermodynamically to four mole of Ag in galena at 300oC and two mole of Ag
at 250oC (Amcoff, 1984). Also, the amount of Ag within galena is commonly comparable
to the amount of Sb, suggesting an affinity between the two elements, as has been
suggested by Amcoff (1984) and shown to occur at close to a 1:1 coupled substitution in
the Macarthur River Pb-Zn-Ag deposit (Croxford and Jephcott, 1972).
A commonly observed feature in all the ore lodes except the Kintore Lode is the
distinct decrease in lead at the very edge of the galena crystal. This may be due to diffusion
of Pb during retrograde alteration at the extremities of the grains. Cd in sphalerite is
highest in 1 Lens, suggesting Cd enrichment within vein style mineralisation. The
underfilling of Fe within pyrrhotite and the overfilling of Fe within pyrite, suggests that
85
Chapter Six – Sulphide Rock Mineral Chemistry
pyrite formation derives from a post-peak high-grade metamorphic interaction of pyrrhotite
with a sulphur-rich fluid, leaving pyrite in the centre of the veins.
The formation of prograde gahnite may have occurred from the desulphidation
breakdown of sphalerite, the reaction of Al-rich clay sediments with Zn-rich fluid or the
metamorphism of silica with Zn-rich hydrothermal clays and carbonates (Plimer, 1987).
86
Chapter Seven – Discussion
Chapter Seven – Discussion The Curnamona Craton represents the surface expression of a polydeformed
Paleoproterozoic intracontinental rift system. The Broken Hill main lode orebody located
within the Broken Hill Block, was deposited as a series of intense episodic pulses of metal-
bearing hydrothermal fluid during rifting. It is the largest accumulation of Pb-Zn-Ag in the
world. After an intense polymetamorphic and deformation history, interpretation of
palaeolithologies central to genetic models is difficult and as a result, many models for the
orebody genesis have been suggested and contested over the years.
This report has documented the B Lode, A Lode and 1 Lens zinc lodes from drill
core and pit, and analysed samples collected during fieldwork for major, trace, rare earth,
halide, stable isotopes, polished section and electron microprobe analysis. The results have
shown that major elements of the zinc lodes show no affinity with regional clastic
metasediments. This disputes early epigenetic models that suggested the orebody formed
via the replacement of clastic sediments (Gustafson et al., 1950), and the recently
described sedimentary expulsion model (Wright et al., 1987). When combined with rare
earth element data, it suggests that the lode horizon and stratabound sulphide rocks are
completely comprised of chemical sediments formed as a submarine hydrothermal
exhalative system during intracontinental rifting. The observed remobilised and deformed
prograde sulphides in association with prograde gangue minerals, suggests that the
sulphide minerals were present prior to metamorphism supporting the syngenetic model
suggested from major and REE geochemistry.
During deformation, sulphides coarsen in grainsize and may move into fold hinges
with corresponding attenuation on the limbs, forming ‘droppers’ within the fold hinges
(Maiden, 1976) which are typically high in Pb and Ag and brecciated from the entrained
gangue minerals. Ore ‘droppers’ have been observed up to 50 metres in length protruding
from fold hinges (Maiden, 1976). The Kintore Lode exposed in the Kintore pit may be an
example of a small-scale dropper where after initially folding some ore is mobilised into
the wall rock were the gangue minerals are brecciated by the injection of the sulphide ore.
The observed brecciation of quartz and garnet crystals in section and higher Pb and Ag
content of the Kintore Lode supports this.
The Kintore Lode is suggested to be the A Lode. Initially the anomalously high Pb,
Zn and Ag grades contained within the Kintore Lode (Table 4.2.1) suggested an affinity
with 2 Lens, as did the rare earth element signatures. The lack of calcite in section within
87
Chapter Seven – Discussion
the Kintore Lode suggested clearly an A Lode origin. The major and trace elements show
that when silica is present in abundance greater than 50 A%, the Kintore Lode and A Lode
closely approximate each other. When silica is less than 50 A% the Kintore Lode may
approximate the 2 Lens or plot independently. It is suggested that as a result of the high
sulphide grade, caused by the movement of sulphides into the fold hinge and possible
‘dropper’ propagation, that the unique geochemistry of A Lode is masked in the Kintore
Lode.
The observation of quartz crystals in the core of gahnite and garnet suggests that
prograde quartz growth was first to occur, followed shortly after, by the prograde growth
of both gahnite and garnet. These observations concur with the suggested two-stage
prograde metamorphic events M1/M2 (Page and Laing, 1992). The observation of garnet
rims around prograde gahnite suggests either prograde garnet growth after gahnite,
suggesting a third prograde event or the growth of garnet during a retrograde event. It has
been suggested (Parr, 1992b) that this is a retrograde reaction caused by the interaction of
gahnite with retrograde fluids. Retrogression has caused the alteration of prograde
sulphides by retrograde biotite, muscovite and chlorite. There is net loss of Ag, possibly
into shear zones (Plimer, 1980) showing that under metamorphism, the system is not
isochemical. Late stage carbonate veins crosscut the ore lodes, resulting in the minor
mobilisation of sulphides, fracturing of gangue minerals and the precipitation of
carbonates, with siderite being the dominant variety in the B Lode veins, and pyrite.
The Broken Hill system is comparable to other ancient systems including the
Pinnacles (Parr, 1992a), Cannington (Bodon, 1996, 1998), Pegmont (Williams et al., 1996)
and Gamsberg (Allen, 1996) where massive sulphides are contained within individual
layers within a amphibolite-granulite metamorphosed and deformed Proterozoic terrain.
The Broken Hill orebody is also comparable with some modern systems, including the Red
Sea (Ross et al., 1969), East Pacific Rise (Michard and Albarede, 1986) and TAG Mound
on the Mid-Atlantic Ridge (Mills and Enderfield, 1995). These modern systems are
exhaling hydrothermal fluid, which shows similar hydrothermal REE signatures to ancient
Broken Hill-type deposits, and have been shown to be precipitating sulphides onto the sea
floor. Investigation of these hydrothermal vents, show that hydrothermal fluids may be
exhaled from both white smokers and black smokers depending on temperature. Within the
Atlantis II Deep basin distal to the hydrothermal exhalation, it has been measured that
there is at least 20m of deposited heavy chemical sediments on the basin floor (Ross et al.,
1969). Deep saline-rich brines have also been identified within the Atlantis II Deep basin,
88
Chapter Seven – Discussion
showing both chemical differentiation (Brewer and Spencer, 1969) and temperature
variation (Ross et al., 1969), both of which have been suggested in models on Broken Hill
to be responsible for the variations in the ore lode geochemical composition, which are
commonly a source of contention between genesis models.
89
Chapter Eight – Conclusions
Chapter Eight – Conclusions The genetic evolution of the Broken Hill Block within the Curnamona Craton began with
the separation of the crust from the mantle between 2100-2300 Ma (McCulloch and
Hensel, 1984). The lower units of the Willyama Supergroup were deposited in a shallow
marine environment with ash fall tuffs, volcanic detritus and feldspathic sand deposition
during the early stages of intracontinental extensional rifting (Stevens et al., 1988).
Deepening of the water profile led to deep-water turbidite sequences in the Thackaringa
Group deposited between 1700-1690 Ma, accompanied by bimodal volcanics and
hydrothermal precipitates occurring during rifting. The deposition of the Broken Hill
Group followed at approximately 1690±5 Ma comprised of further bimodal volcanics,
hydrothermal precipitates and clastic sedimentation (Page and Laing, 1992). Upon the
cessation of extensional rifting and hydrothermal activity, the rift was rapidly filled by
deep marine tubiditic and carbonate sequences of the Sundown Group, followed by the
deposition of platform shelf sequences of the Paragon Group at approximately 1676±10
Ma.
Hydrothermally-derived exhalative chemical sedimentation occurred as a number
of intense episodic pulses. This produced minor orebodies within the Thackaringa Group,
such as the Pinnacles deposit in the Cues Formation comprising five distinct zinc and lead
lodes and major stratiform orebodies in the Broken Hill Group including the Western
Mineralisation in the Parnell Formation and main ‘Line of Lode’ in the Hores Gneiss,
which contains the B Lode, A Lode and 1 Lens documented by this study. The zinc lodes
show no correlation with regional Broken Hill clastic metasediments of Slack and Stevens
(1994), yet exhibit a distinctive hydrothermal REE signature. This suggests that these ore
lodes are almost entirely comprised of hydrothermal chemical precipitates being deposited
rapidly during a period of low clastic input. Each zinc lode has its own unique geochemical
and mineralogical compositions indicating variation related to the initial composition of
the chemical precipitates, pre-metamorphic alteration, or from differentiation during later
partial melting and mobilisation.
After deposition, the Willyama Supergroup was subject to multiple regional
deformation and metamorphic events beginning with the peak prograde D1/M1 event at
1600 Ma. This resulted in the overturning of the Broken Hill orebody, involving partial
melting and remobilisation of the ore and growth of associated quartz-gahnite and quartz-
garnet alteration halos. The second peak prograde event D2/M2 followed, resulting in F2
90
Chapter Eight – Conclusions
fold structures and promoted the remobilisation of ore into fold hinges for a corresponding
attenuation of ore along the fold limbs. During the initial stages of the retrogression, the
M3 event occurred between 1600-1570 Ma, which included F3 and F4 folds, produced
further quartz-garnet alteration including garnet rims overgrowing prograde gahnite and
the remobilisation of ore into F3/F4 fold hinges as observed in the A Lode within the
Kintore pit. During the final stages of the M3 retrograde metamorphic event, formation of
numerous steeply dipping retrograde shear zones occurred, enriched in remobilised Ag-
rich ore, liberated by the retrograde breakdown of argentian tetrahedrite.
Pegmatites and granites were emplaced in the region about 1420+20 Ma, followed
by a thermal pulse of approximately 300-400oC between 1250-1100 Ma during the
Grenville Orogeny causing regional uplift, shear zone reactivation, carbonate vein
propagation through the orebodies including B Lode and further movement of Ag into
shear zones. Prolonged erosion and some accompanying sedimentary deposition between
1100 Ma and 600 Ma, was followed by dolerite and pyroxenite dykes intruding close to
830 Ma. Further emplacement of ultrabasic dykes and plugs around 561+7 Ma preceded a
low-grade retrogression event during the Delamerian Orogeny at 520+4 Ma, causing
reactivation of retrograde shear zones along with the emplacement of further pegmatites.
Minor fault movement in shear zones, further erosion, uplift and regolith weathering has
continued in the region to the present day.
91
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