Chapter 1 Introduction
Chapter 1 Introduction
*
SEDIMENT HOSTED B et
m
*
MnO2
POLYMETALIC Ag-Au
POLYMETALIC Au-Ag
QUARTZ SULPHIDE Au + Cu
limestone marl S
WALLROCK
PORPHYRY Au-Cu
MINERALIZATION S S
PORPHYRY Cu-Au
Banded tension vein REPLACEMENT FLUIDS
Fissure vein Rising mineralised
EXOSKARN magmatic fluid
S Sheeted vein
Circulating meteoric-
Stockwork vein dominant water
Breccia fill Collapsing evolved fluid
A - low Ph
Lithological control
B - bicarbonate
Disseminated ENDOSKARN O - oxygenated
* Fluid mixing
Corbett Model_2017
Rising volatiles
Figure 1.1 Conceptual model for the styles of epithermal Au-Ag and porphyry Cu-Au mineralisation developed in subduction-related
magmatic arc – back arc settings.
tka
u ko
- Ch
sk
ot
v
O kh v
ol- 0.7 v
ng 6
Mo
v v
v
v
v
OB
v
v v v
8 6
v
v
OR
Subduction zone
v
v
v
v
v
v
v
10
Spreading centre
Sa
v
A
Transform fault
n
v
nd
v
re
v
Orthogonal convergence
v
as
v 0.3 4
OR
F
v
8 OB
v
v
v
Philippine
Oblique convergence
vv
OB
v
8 Plate 10.7
v
8
v
0.3
v
v v
v
OB
v
4
v
v OR v
8
Direction and rate of
v v v
v
Eurasia v
6
v
5
vv
Plate
v
v
v
v
Solomon
v
v
v 10
OB
v
Plate
v
v
v
v v v
Magmatic arc
v
v v
7 0.3 10.2
v
v
Pacific
v
v v v
7.7
v
v
v
v
Plate
v
v
v
v
v
OR
Back arc
v
8 v
v v
v
v v
7 10
v
OR
v
v
v 6
v
Australia-India v
Nazca
v
Plate
v
5 10
Plate 6.5
v
v
v
5 OR
v
10
10
v
8 v 6.5
v
OB
v
7
v
v
v
v
v
6
v
v
v
v
v
v
0 2000 km
Adapted from Curcum-Pacific Council
or Energy and Mineral Resources, 1981. CORBETT ai1634
Figure 1.2 Pacific rim tectonic plates, magmatic island arcs, back arcs and spreading centres.
magmatic
ARC BACK ARC
solfatara
LOW SULPHIDATION
Au-Ag
HIGH SULPHIDATION hot spring
Au
F
travertine
steam heated 200
alteration
acid sulphate
felsic
bicarbonate waters caps
domes
eruption breccia
Carbonate-base Epithermal
silica
metal Au quartz Au
sinter
Quartz-sulphide +
D veins D veins waters
Au±Cu eteoric 200 chalcedony
c -m -ginguro
ati
gm
PORPHYRY Cu-Au ma Au-Ag
0
20
felsic
volcanics polymetallic
Ag-Au
Volatiles
Composite magmatic-
meteoric fluids
m et
e o r i c w a te r s
CORBETT ai1534
Figure 1.4 Ore systems within subduction-related magmatic arc and back arc settings.
(Mitchell and Leach, 1991; Corbett and Leach, 1998) ppm Cl as reflected in fluid inclusion salinity studies
which lie within andesitic arcs, are driven by shallow (Corbett and Leach, 1998 and references therein).
level porphyry Cu style intrusion heat sources related Giggenbach (1997) also noted the significantly higher
to deeper magmatic bodies, and feature more saline CO2 concentrations in andesitic magmatic arcs
fluids (figure 1.5). Whereas the New Zealand systems (Philippine) than continental rifts (New Zealand)
contain only 3-4% magmatic component such as and this CO2 features in arc-related low sulphidation
<1000-2000 ppm Cl, the Philippine systems contain epithermal deposits. Terry Leach demonstrated that
up to 50% magmatic component and >10,000-50,000 although there is a greater emphasis upon the New
s
bicarbonate
te r
-1 -1
intrusions
wa
waters
m e t e o ric
-2 conductive convective -2
me
heat transfer zone
teo
ric
-3 -3
wa
s
te
r
-4 -4
rising chloride
waters
--5 --5
magma source
-6 -6
-7
degassing -7
magma
-8 -8
CORBETT ai1535
Figure 1.5 Comparison of subduction-related magmatic arc and back arc geothermal systems, drawn at the same scale, from data
within Corbett and Leach (1998).
Zealand geothermal systems in many published vary with deposit type and some mineralisation styles
exploration models, the Philippine geothermal systems will be prioritised higher than others in different
provide better analogies to many epithermal-porphyry exploration programs.
ore deposits. Hence, fluid mixing models, some of
which feature CO2, provide better mechanisms for 1.2.1 Evolution of terminology
bonanza Au deposition than boiling models (Leach and
Corbett, 2008; section 7.5). Waldemar Lindgren (1922) defined the term
epithermal as hydrothermal deposits “formed by
1.2 CLASSIFICATION OF SUBDUCTION ascending hot waters near the surface in or near
RELATED ORE SYSTEMS effusive rocks at relatively low temperatures and
pressures”, and subsequently placed limits upon
A classification, derived from analyses of many epithermal deposit formation as < 1000 m depth
exploration projects and mines, aids in the distinction and < 200°C temperature (Lindgren, 1933, p. 454-5).
of different Au-Cu deposit types which display As Lindgren’s classification (op cit) appeared to be
varying characteristics such as: zoned wall rock influenced by shallow level hot spring deposits, the
alteration, geochemical and geophysical properties term epithermal is now extended to much deeper
during mineral exploration, metallurgical responses crustal levels approaching the porphyry environment,
during treatment, and overall value (potential metal and so includes higher temperature deposits that some
grades and size). Linkages occur between deposit workers might have formerly termed mesothermal. The
types which are presented here (figures 1.1 & 1.4) as term ‘deep epithermal’ may be employed for deposits
points within a continuum of deposit types at varying such as low sulphidation epithermal quartz-sulphide
crustal levels and/or tectonic settings. It is therefore Au ± Cu mineralisation which are locally analogous to
important to distinguish different deposit types, early D veins (figure 1.4), in the classification of Gustafson
in any exploration program in order to consider the and Hunt (1975).
exploration implications of the ore type classification
described above. For instance, exploration methods The rise in Au price in the early 1980’s prompted
Polymetallic Ag-Au
barren advanced
Quartz-sulphide
e rs
argillic alteration
s
Au±Cu
id
at
ic w
ral flu
m ete o r
disproportiation of magmatic SO2
neut
magmatic
s
4SO2 + 4H2O 3H2SO2 + H2S
volatiles ticl fluid
near
H2O, CO2 Acid sulphate
alteration
magma
Figure 1.6 Fluid flow paths for low and high sulphidation epithermal Au deposits (modified from Corbett and Leach, 1998).
distinguishes between low and high sulphidation Au-Ag bearing sulphides, rises, it may combine with
epithermal mineralisation styles developed from two varying quantities of shallower circulating meteoric
profoundly different evolving ore fluid types, which waters and other evolved fluids, which deposit much
might be simplistically considered to originate as of the gangue such as quartz, adularia or carbonate.
open or closed systems (figure 1.6). Low sulphidation The two low sulphidation epithermal deposit groups
fluids develop in an open system in equilibrium with introduced above are distinguished by the magmatic
the wall rocks, as rising near neutral magmatic fluids versus meteoric contents of the ore fluid. There is
are diluted by variable entrainment within circulating a significantly higher magmatic fluid component in
meteoric waters. By contrast, the fluids which deposit the intrusion-related sulphide-rich deposits typical
high sulphidation epithermal ores might be considered of arcs, and the stronger meteoric component in the
to rise from the magmatic source at depth as a closed sulphide-poor banded quartz vein deposits typical of
bubble, not in equilibrium with the wall rocks, and extensional settings. A comparison of figures 1.1, 1.4
evolve to take on an acidic character, prior to later and 1.5 illustrates the settings of the two groups of
cooling and neutralisation by wall rock reaction (section low sulphidation epithermal Au-Ag deposits in the two
2.2.4.4). Each epithermal mineralisation style might tectonic environments (arcs and back arc or rift).
now be defined as derived from a distinctly different
hydrothermal fluid and display characteristic ore and 1.2.2.1.1 Low sulphidation fluids
gangue mineralogy as well as wall rock alteration, rather
than the original definition based on the sulphidation The synthesis (Corbett and Leach, 1998) of studies
state of specific ore minerals. Confusion created by from the back arc Taupo Volcanic Zone geothermal
the incorrect application of the term intermediate in New Zealand (Henley and Ellis, 1983; Simmons
sulphidation is resolved below. and Brown, 2000a; Simpson et al., 2001 and references
therein) with Philippine arc geothermal systems
1.2.2.1 Low sulphidation epithermal Au-Ag (Mitchell and Leach, 1991; Reyes, et al., 1993;
Giggenbach, 1997; Corbett and Leach, 1998) provides
Low sulphidiation epithermal Au-Ag mineralisation three fluid types (figure 1.7):
is deposited from evolving near neutral composite • Neutral chloride
magmatic-meteoric ore fluids in which S occurs as H2S. • Bicarbonate waters
In essence, as an evolving magmatic fluid, which hosts • Acid sulphate waters
Corbett Short Course Manual Section 1 7
Low sulphidation High sulphidation
Fluid Dilute, S as H2S Saline S as SO2
Wall rock Local early propylitic with dominance zoned advanced argillic - argillic as vughy silica-
alteration of zoned argillic illite Gp with quartz, >alunite Gp->kaolin Gp->illite Gp, and abundant
carbonate, pyrite pyrite
Ore Low sulphide < 2% (locally <5%) Enargite-pyrite with low temperature luzonite
minerals Pyrite, sphalerite (variable Fe:Zn), galena, and varying to covellite, chalcocite, bornite,
chalcopyrite, Ag sulphosalts chalcopyrite at depth
Table 1.2 Comparison of low and high sulphidation epithermal, modified from Corbett & Leach (1998).
kaolin, cristobalite,
alunite, pyrite sulphur solfatara
* CO2
CO2
*
mixing
tuff
me
or
te
ic
w a te rs
*
te
rs
a
quartz, K-feldspar (adularia), m ete o ri c w
chlorite, illite, carbonate, pyrite alteration
quartz, K-feldspar (adularia),
chlorite, illite, carbonate, pyrite alteration
me
ic
w a te rs
Figure 1.7 Evolved low sulphidation style hydrothermal fluids in magmatic arc and back arc settings.
BRECCIA C O
B B
S
LITHOLOGICAL
A
STRUCTURAL B S EPITHERMAL BANDED CHALCEDONY GINGURO Au-Ag * O
*
SEDIMENT HOSTED B et
m
CARBONATE-BASE METAL Au eor
REPLACEMENT Au ic w a t e r
*
MnO2 A
POLYMETALIC Ag-Au
POLYMETALIC Au-Ag
QUARTZ SULPHIDE Au + Cu
B
limestone marl S
WALLROCK
PORPHYRY Au-Cu
MINERALIZATION S S
PORPHYRY Cu-Au
Banded tension vein REPLACEMENT FLUIDS
Fissure vein Rising mineralised
EXOSKARN magmatic fluid
S Sheeted vein
Circulating meteoric-
Stockwork vein dominant water
Breccia fill Collapsing evolved fluid
A - low Ph
Lithological control
B - bicarbonate
Disseminated ENDOSKARN O - oxygenated
* Fluid mixing
Corbett Model_2013F
Rising volatiles
Figure 1.8 Low sulphidation epithermal Au fluid flow trends recognised in different terrains.
In path A, typically in compressional magmatic island arcs of the Southwest Pacific rim, ore fluids deposit mineralisation in order
characterised as: quartz-sulphide Au ± Cu, overprinted by carbonate-base metal Au which in turn evolves to epithermal quartz Au.
In path B developed in strongly extensional settings such as the Sierra Madre of Mexico, Southern Peru or Argentine Patagonia, quartz-
sulphide Au evolves to the polymetallic Ag-Au variant of carbonate-base metal Au, and then banded chalcedony-ginguro Au-Ag veins
as substantial meteoric waters deposit chalcedony-adularia and the sulphide vein portion evolves to form ginguro bands. Chalcedony-
ginguro Au-Ag veins also occur in the SW Pacific where they bottom as base metal sulphide-rich quartz veins.
Fluid flow path C represents the rare case where a high sulphidation fluid might become sufficiently neutralised to form a lower
sulphidation fluid and deposit ores typical of carbonate-base metal Au and epithermal quartz Au mineralisation.
Neutral fluids which rise by convective flow from 2000a), where Terry Leach (pers. commun.) noted fluid
buried magmatic source rocks contain CO2 and Cl, mixing provided the deposition of anomalous gold. At
in far greater proportions in arc (Philippine) than rift shallow levels in the vadose zone (aerated region above
(New Zealand) environments (above and Corbett the saturated phreatic zone, figure 1.5) H2S gas derived
and Leach, 1998; Simmons and Browne, 2000a; from the deeper two-phase zone is oxidised to produce
Giggenbach, 1997). In arc environments deep acid sulphate waters, which contain sulphuric
hydrothermal fluids rise and react with the wall rock acid, while oxidation of H2S in the atmosphere
to provide alteration assemblages grading from potassic produces native sulphur and steam (Corbett and Leach,
to propylitic at depth and chlorite-zeolite at 1998). Thus, there are two end member (bicarbonate
shallow levels (Corbett and Leach, 1998). In shallow and acid sulphate) evolved waters derived from the
level outflow zones, when vapour pressure of the original neutral chloride precursor (figure 1.7). The
rising fluid eventually exceeds confining pressure, bicarbonate waters, which are more abundant in arc
water vapour and other gasses (mainly CO2 and lesser than rift settings and associated with the formation
H2S) exsolve from the hydrothermal fluid. Then in of carbonate-base metal Au deposits, show empirical
the two-phase zone, absorption of CO2 by ground relationship with high level felsic (dacite) domes as a
waters produces moderately low pH bicarbonate possible link to the magmatic source for CO2 and H2S.
waters (Corbett and Leach, 1998). In magmatic arcs the There is an exploration implication that elevated
abundant bicarbonate waters may vent to form surficial Au grades result from the effective destabilization of
travertine deposits, and are apparent on the margins of bisulphide complexes which transport Au, as oxidising
the rift Ohaaki-Broadlands geothermal system in New low pH bicarbonate and acid sulphate waters mix with
Zealand (Hedenquist, 1990; Simmons and Browne, rising ore fluids (section 7.5; Leach and Corbett, 2008).
RIFT phreatic
breccia
sinter
EPITHERMAL travertine
diatreme acid sulphate
QUARTZ Au alteration
A A
B B
O S
A
B S EPITHERMAL BANDED CHALCEDONY GINGURO Au-Ag * O
C
*
B et
m
CARBONATE-BASE METAL Au eor
ic w a t e r
*
MnO2 POLYMETALIC Ag-Au
POLYMETALIC Au-Ag
QUARTZ SULPHIDE Au + Cu
WALLROCK
PORPHYRY Au-Cu
S S
PORPHYRY Cu-Au
D FLUIDS
Rising mineralised
magmatic fluid
Circulating meteoric-
dominant water
Collapsing evolved fluid
A - low Ph
B - bicarbonate
O - oxygenated
Rising volatiles
Corbett Model_2013A1
Figure 1.9 Low sulphidation epithermal Au mineralisation styles develop within magmatic arcs as the ore fluid evolves from early to late
and deep to shallow crustal levels.
A - Modified figure 1.1 to illustrate the fluid flow and paragenetic sequence for the formation of mineralisation styles.
B- Quartz-sulphide Au + Cu mineralisation is characterised by quartz and coarse crystalline auriferous pyrite, from Bilimoia, Papua New
Guinea.
C - Carbonate base-metal Au comprises early pyrite (of the quartz-sulphide Au + Cu event) followed sphalerite (here dark Fe-rich) with
lesser galena and later carbonate, here as open space breccia fill, from Kelian, Indonesia.
D - Epithermal quartz Au mineralisation is characterised by bonanza grade high fineness yellow free gold with quartz and green
roscoelite (V illite) gangue, from Porgera Zone VII, Papua New Guinea.
B EPITHERMAL Au
HIGH SULPHIDATION A C
LOW SULPHIDATION EPITHERMAL Au-Ag
steam heated
alteration permeable
RIFT phreatic
diatreme horizon
breccia
sinter
silica EPITHERMAL travertine
diatreme acid sulphate
QUARTZ Au alteration
A A
B B
BRECCIA O S
LITHOLOGICAL
A
STRUCTURAL B S EPITHERMAL BANDED CHALCEDONY GINGURO Au-Ag * O
*
SEDIMENT HOSTED B et
m
*
MnO2
POLYMETALIC Ag-Au
POLYMETALIC Au-Ag
QUARTZ SULPHIDE Au + Cu
limestone marl S
WALLROCK
PORPHYRY Au-Cu
MINERALIZATION S S
PORPHYRY Cu-Au
Banded tension vein REPLACEMENT FLUIDS
Fissure vein Rising mineralised
EXOSKARN magmatic fluid
S Sheeted vein
Circulating meteoric-
Stockwork vein dominant water
Breccia fill Collapsing evolved fluid
A - low Ph
Lithological control
B - bicarbonate
Disseminated ENDOSKARN O - oxygenated
* Fluid mixing
Corbett Model_2013E
Rising volatiles
Table 1.3 Field characteristics of different low sulphidation epithermal Au-Ag styles.
Table 1.4 Essential differences between the low sulphidation carbonate-base metal Au and polymetallic Ag-Au deposits.
Table 1.5 Comparison of the two end members of low sulphidation epithermal Au-Ag mineralisation.
RIFT phreatic
breccia
sinter
EPITHERMAL travertine
diatreme acid sulphate
QUARTZ Au alteration
A A
B B
O S
A
B S EPITHERMAL BANDED CHALCEDONY GINGURO Au-Ag * O
*
B et
m
eor
B
CARBONATE-BASE METAL Au ic w a t e r
*
MnO2 POLYMETALIC Ag-Au
POLYMETALIC Au-Ag
QUARTZ SULPHIDE Au + Cu
WALLROCK
PORPHYRY Au-Cu
S S
PORPHYRY Cu-Au
C FLUIDS
Rising mineralised
magmatic fluid
Circulating meteoric-
dominant water
Collapsing evolved fluid
A - low Ph
B - bicarbonate
O - oxygenated
Rising volatiles
Corbett Model_2013B1
Figure 1.11 Evolution of low sulphidation epithermal mineralisation styles within strongly extensional settings such as back arcs or rifts
(Sierra Madre of Mexico, Southern Peru or Argentine Patagonia).
A - In strongly extensional settings the banded chalcedony-ginguro Au-Ag veins develop as the ore fluid evolves and combines with
meteoric waters which deposit chalcedony, adularia and quartz after platy calcite interlayered in veins, such as this example from
Golden Cross, New Zealand. Note the symmetry in the bands and central open space as these veins grow inwards as open space fill.
B - Some polymetallic Ag-Au deposits evolve to host late stage mineralisation characterised by argentite-acanthite, pyrite and white
Fe-poor sphalerite, such as this example from Juevos Verde, Argentine Patagonia.
C - Polymetallic Ag-Au mineralisation is characterised by pyrite (as part of the early quartz-sulphide Au + Cu component, locally with
barite) along with sphalerite (here yellow low to moderate Fe), galena and Ag sulphosalts with gangue of quartz and carbonate (here
rhodochrosite). This sample from Caylloma mine, Peru, assayed 30,00g/t Ag, contained mostly within dark freibergite, the Ag-rich
tetrahedrite.
andesite
Silica-alunite
Pyrophyllite - diaspore
structure
Dickite-kaolinite ± illite
CORBETT ai1674
C D E
F H G
Figure 1.12 High sulphidation epithermal Au mineralisation is associated with characteristic zoned advanced argillic alteration grading
outwards from the core of the alteration system.
A – Graphic illustrates the localisation of a high sulphidation epithermal system at the intersection of a feeder structure and permeable
lithology which then controls fluid flow (see figure 1.1) and alteration zonation. Mineralisation overprints the competent residual vughy
silica.
B - Vughy silica at the centre of the advanced argillic alteration zone, from Sappes, Greece.
C - Silica-alunite grading outwards from the centre, from Sappes, Greece.
D - Pyrophyllite-diaspore in the outer portion of the advanced argillic alteration, from Sappes, Greece.
E - Dickite-kaolinite grading outwards to illite then more marginal smectite discernible as a swelling clay as the argillic halo to advanced
argillic alteration, from Sappes, Greece.
F - Mineralisation post-dates alteration as breccia fill (black) enargite with additional (white) alunite, from Nena, Papua New Guinea.
G - Disseminated enargite-pyrite within vughy silica, from Mt Kasi, Fiji.
H - Enargite-pyrite vein cuts vughy silica, from Cerro Quema, Panama.
as it rises and so by the stage it has reached epithermal Wafi-Golpu, Papua New Guinea).
levels it might be characterised by a pH of 0-2 and
temperature of 250-300°C. This environment in which In the epithermal regime the hot acidic fluid is
fluid evolution occurs provides a distinct gap between progressively cooled and neutralised by wall rock
any high sulphidation epithermal Au deposit and its reaction to provide the characteristic zoned advanced
underlying intrusion source (figures 1.1 & 1.4), in the argillic hydrothermal alteration grading outwards
order of several hundres metres. The exploration from residual (vughy) silica to mineral assemblages
implication is that high sulphidation epithermal Au dominated by alunite, pyrophyllite, dickite and so on
deposits do not immediately overlie source intrusions with variations described in detail later (section 2.2.4.4;
as illustrated in some ore deposit models. However, figure 1.12). The hot acidic fluid breaks up into two
many high sulphidation epithermal Au deposits may phases. A faster moving volatile-rich phase reacts
sit on top of older intrusions, possibly telescoped in with the wall rocks to provide the characteristic zoned
conditions of rapid uplift and erosion (Caspiche, Chile; advanced argillic alteration by progressive wall rock
Corbett Short Course Manual Section 1 15
reaction. The slower liquid-rich phase deposits later fluids responsible for kaolin alteration styles commonly
Au-Ag mineralisation within sulphides comprising collapse into deeper levels in the hydrothermal system
pyrite and enargite, or luzonite, its low temperature where they might mix with rising ore fluids and
polymorph, along with barite-alunite gangue discussed promote the development of high precious metal grade
in detail later (section 8.3; figure 1.12). At epithermal mineralisation discussed herein.
crustal levels hydrothermal fluid flow in the wall rocks
is controlled by permeable lithologies, breccias or 1.2.2.4 Does intermediate sulphidation exist?
structure (figure 1.1, section 8).
The acidic fluids associated with high sulphidation
The early 1980’s term ‘acid sulphate, which is now epithermal Au deposits locally become cooled and
replaced by high sulphidation for epithermal Au neutralised to form lower sulphidation states late in
deposits of that type, is maintained for kaolin-alunite the paragenetic sequence, and/or at the margins of
bearing blankets of alteration developed near the some high sulphidation epithermal Au deposits (fluid
palaeo surface as caps to low sulphidation Au-Ag flow path C in figure 1.8). This has been described for
deposits (section 2.2.4.5). Similar near palaeo surficial Link Zone at the margin of the Wafi high sulphidation
caps to high sulphidation epithermal Au deposits Au deposit, Papua New Guinea (section 8.6.6; Leach,
are termed steam heated alteration, characterised by 1999) and at El Indio mine district, Chile (section
cristobalite, kaolin and powdery alunite and basal silica 8.6.1; Corbett and Leach, unpubl. reports, 2000 in
ledges (figure 1.1; section 2.2.4.5). Near surficial acidic Heberlein, 2008). At the Viento vein system (figure
A B
Dilational
ore environments shoot 4
link B
flexure
structures shoot 3 C
C
shoot 2 D
El Indio Mine
3965 level
0 100m Viento veins
El Indio
veins
shoot 1 E
Campana D
o
uan
Paih
fluid flow
mined
F
Faults 0 250m
Copper veins
Gold veins
CORBETT ai1672a
Figure 1.13 Transition from high to lower sulphidation at the El Indio-Viento veins, Chile, showing the trend in mineralogy in space and
time.
A - Sketch map of the El Indio-Viento vein system showing the sigmoidal loop mapped by Stan Caddy at El Indio, from Jannas et al.
(1990), and the Viento veins with ore shoots, from Corbett unpubl. reports (2000) in Heberlein (2008).
B - Quartz-Au (shoot 4).
C - Quartz-rhodochrosite-sphalerite-galena (shoots 2 & 3).
D - Enargite-luzonite (mined & shoot 1).
E - Banded enargite-pyrite ore at the El Indio veins shown in green on the graphic.
F - Bonanza quartz-Au El Indio ore shown in red in the graphic.
B D
Figure 1.14 Some characteristics of porphyry Cu-Au deposits discussed in detail in section 5.
A - Typical porphyritic host rock, Woodlark Is., Papua New Guinea.
B - Stockwork (M style) laminated quartz-magnetite veins, from Copper Hill Australia.
C - Stockwork of several overprinting vein events from the Ridgeway porphyry , Australia.
D - Wallrock porphyry as interpreted sheeted veins outside the source intrusion, Cadia Hill, Australia.
km below the palaeo surface. While porphyry deposits compositions and display variations in form Corbett
typically display characteristic paragenetic sequences et al., 2009). Au-rich variants, termed porphyry Cu-
of zoned hydrothermal alteration and vein styles, best Au deposits are recognised in many settings (Sillitoe,
metal grades are associated with those systems which 1993, 2000). Some workers have focused upon K-rich
feature multiple intrusions and hence polyphasal intrusion compositions with Au mineralisation (Müller
mineralisation events, although post-mineral intrusions and Groves, 1993, 2000, 2016), while others the
may stope out ore. (figure 5.1 section 5). influence of oceanic crust in their formation (Cooke
et al., 2002; 2014), and arc reversal and remelting
This work expands upon existing porphyry definitions or oceanic crust (Solomon, 1990). Gold porphyry
with reference to the exploration implications of deposits, although with local anomalous Cu and Mo,
structure and the paragenetic sequence porphyry might be distinguished as those mined for only Au,
alteration and mineralisation expanded from earlier as the primary mineralisation, or a possible overprint
work by Corbett and Leach (1998). Dilatant fracture (Fort Knox, Alaska, section 5.3.2.3). Suggested Sn and
systems host sheeted quartz-sulphide veins which W-rich porphyry styles (Seedorff et al., 2005) would
transport mineralisation from magmatic source rocks need to display porphyry alteration and mineralisation
at depth to higher crustal level cooler sites of mineral styles in order to be included in this class.
deposition. Porphyry Cu deposits display characteristic
hydrothermal alteration which is zoned in space and The term ‘wallrock porphyry deposits’ (Newcrest
time analysed as a major component of this study Mining Staff, 1996) has been used for Au-rich porphyry
(section 5). This zoned hydrothermal alteration, Cu-Au style mineralisation developed wholly within the
along with marginal veins and pebble dykes may wall rocks outside the source intrusion, which may not
be used as vectors towards buried porphyry targets have been identified, as different to the more limited
(section 9). Ore hosting quartz-sulphide veins are also mineralisation normally documented extending from
characterised as different vein styles which consistently a mineralised porphyry into the adjacent wall rocks
display the same paragenetic sequence of formation. (Cadia Hill & Cadia East, Australia; Gaby, Ecuador;
Spine-like mineralised stocks may cluster above more some Maricunga belt occurrences, figure 5.2). Some
deeply buried magma sources commonly aligned along deposits classed as Au porphyry might represent
regional structures (Goonumbla & Cadia, Australia). intrusion wall rock hosted deep epithermal low
sulphidation quartz-sulphide Au ± Cu mineralisation.
While Mo is recognised in many porphyry Cu deposits,
a separate group of porphyry Mo deposits (White et
al., 1981) are associated with more granitic porphyry