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Documente Profesional
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MINERALIUM
DEPOSITA
9 Springer-Verlag 1996
211
150o17'E
t
oxygen
General geology
==,
!Carboniferous)
~\ StrikeandD'p
Fig. 1. Simplified geological map of the Cracow gold field. (Modified from Brooks 1974 and Worsley 1992)
Analytical techniques
Microprobe analysis
Electron m i c r o p r o b e analyses were performed on a Jeol840A instrument at James C o o k University. An accelerating voltage of 25 K V for sulphides, counting time of 60
seconds and a b e a m current of 15 nA was used. A Z F
corrections were carried out by T r a c o r N o r t h e r n M i c r o Q
software.
212
Table 1. Characteristics of the deposits at Cracow
Stage
Mineralogy
Ore
Pyrite
Sphalerite
Galena
Chalcopyrite
Hessite(Ag2Te)
Altaite (PbTe)
AuAgTellurides
Electrum (AuAg)
Gangue
Quartz
Adularia
Calcite
Sericite
Chlorite
Zeolite
Vein texture
I
D C R (K)
r r
M MM
r r
I1
D C R K
m
C
C
C
m
r
t
t
m m m
m
m
m
m 9 9
r
t
r t t
MMMM
m C m m
C C
r m
r m
IlI
(D) C R (K)
r r
IV
D C (R) (K)
D C (R)(K)
r r
t t
r r
M C
m C
C
m
MM
MM
r
Stockwork
Crustiform
Massive
Veinlet
Veinlet
D, Dawn; C, Central Extended; R, Rose's Pride; K, Klondyke; (), Stage is absent or is not observed; M, Major; C, common; m, minor; r, rare;
t, trace
based on the comparison of paragenesis of each deposit,
and also based on cross-checking with the paragenesis at
Golden Plateau which has been well documented by Worsley (1992). The main characteristic features of each stage
at individual deposits are summarised in Table 1, and
some examples of crosscutting relationships are illustrated
in Fig. 2.
213
214
been synchronous. Comparing with the main Golden Plateau lode, the outside lodes contain much better developed Stage II gold mineralisation, characterised by
crustiform and cockade banding. This may be attributed
to more extensive brecciations during Stage III at Golden
Plateau, which destroyed continuous bands of Stage II
and gave a more massive character to the Golden Plateau
lode overall.
Gangue mineralogy
In general, Stage II of each lode has its own predominant
gangue mineral assemblage (see Table 1). The most distinct difference is that the ore bodies in the west part of the
Cracow district (Klondyke and Rose's Pride) contain significant amounts of calcite, whereas calcite is absent in
Stage II of other ore bodies. Vein sericite, adularia and
chlorite are present nearly everywhere but adularia and
chlorite are the most abundant at Central Extended.
GoM mineralisation
Locations
Gold mineralisation is best developed at Central Extended among the studied deposits, where patches rich in
electrum, usually associated with rhombic adularia and
fine-grained quartz with recrystallisation textures, are often observed in polished thin sections, and where high
gold grades exceeding 10 g/t are frequently indicated by
assays from drill cores and rock chips. At other deposits,
electrum, which is commonly sparsely distributed, is very
difficult to be detected in polished thin sections, and the
gold tenors are usually less than 10 g/t.
Quartz textures
Crystalline
Microcrystalline
Chalcedonic
Massive
Crustiform
Colloform
Moss
Comb
Zonal
Mosaic
Feathery
Flamboyant
Ghost-sphere
Saccharoidal
Pseudo-acicular
Pseudo-bladed
Varieties of adularia
Sub-rhombic
Rhombic
Tabular
Pseudo-aicular
DA
CE
****
**
*
****
*
****
****
***
***
**
*
***
*
**
***
****
**
*
**
****
**
*
****
**
*
RP
KL
****
**
**
***
***
**
****
**
**
****
***
**
*
*
**
***
**
*
*
**
***
***
***
**
**
Quartz textures
A classification of quartz textures in epithermal veins from
Queensland has been developed (Dong et al. 1995). This
classification can be well applied in the Cracow gold field.
The crustiform texture is diagnostic of Stage II throughout the district (see Fig. 2). Additionally, coarse comb
texture predominates only at Dawn (Fig. 3a). The primary
and recrystallisation textures possibly inherited from silica gel, including colloform, moss, ghost-sphere, flamboyant and mosaic textures (Fig. 3b, c and d) are best developed and widespread at Central Extended. In addition,
215
microcrystalline comb, feathery, pseudo-acicular and
chalcedonic textures are present locally. The textural assemblage at Klondyke and Rose's Pride is characterised
by replacement textures including saccharoidal (Fig. 3e)
and pseudo-acicular (Fig. 3f).
<
Adularia textures
0
<
0
I I I I
<
2~
I I I I
;>
<
I I I I
~ O ~ O
0~
.9
='~
~D t D ~ O O
e"
O
o
0
<<
Monophase liquid inclusions are predominant and abundant in quartz crystals. The lack of vapour bubbles in this
type of inclusion probably results from metastable nucleation due to their small sizes of <2 ~tm (Roedder 1984).
Liquid-rich inclusions are commonly seen in calcite and
216
217
218
Table 4. Fluid inclusion data from Stage II veins
Sample Host
Location
no.
mineral
RL"
(metres)
Th (~
Range
Average
Tmice (~
Range
KL21
KL52
Cal
Cal
KL waste dump
KL outcrop
280-320
320
181 to 211
153 to 189
202.4 (42)
171.5 (11)
0.0 to - 0.1
- 0.1 (18)
0.18
RP66
RP49
Cal
Cal
RP RPD9/154.2
RP outcrop
159
290
187 to 226
162 to 183
211.7 (20)
171.6 (12)
- 0.0 to
0.2
- 0.0 to - 0.2
- 0.1 (20)
- 0.1 (3)
0.18
0.18
CE16
CE04
Adu
Qtz
CE WHD30/65.5
CE open pit
335
375
264 to 278
247 to 269
271.4 (8)
252.1 (7)
- 0.3 to - 0.6
- 0.4 to - 0.6
- 0.5 (5)
- 0.6 (4)
0.87
1.05
DA64
DA08
Qtz
Sph
Dawn NS64/54.7m
Dawn waste dump
275
285-305
254 to 285
264 to 287
270.3 (8)
271.0 (12)
- 0.2 to - 0.4
- 0.2 to - 0.3
- 0.3 (7)
- 0.2 (7)
0.53
0.35
Average
Equiv.b
wt% NaCI
Cal, Calcite; Adu, Adularia; Qtz, Quartz; KL, Klondyke; RP, Rose's Pride; CE, Central Extended
"Elevations of the samples, it has been assumed that the samples from waste dumps came from between the lowest level of the mining and the
present surface
bCalculated from Potter et al. (1978)
219
Table
Sample
Location
Mineral
T (~
Minerals
Fluid ~
1~lSOsMow 613CpDB
%
%0
~lSOH20
(~13C1
(~13C2
%0
%0
%0
no.
DA08
DA10
Qtz
Qtz
270
270 b
- 3.22
- - 3.97
11.8
12.5
CE22
CE16
CE04
CE, WHD28/58.1m
CE, WHD30/64.5m
CE, open pit
Qtz
Qtz
Qtz
230~
230~
210~
- 3.09
- 2.99
- 1.44
13.5
13.4
13.0
RP49-1
RP49-2
RP, outcrop
As above
Qtz
Cal
170e
170
- 2.06
- 6.66
- 6.23
16.4
17.4
7.0
8.2
KL52-1
KL52-2
KLB1
RPB1
KL, outcrop
As above
Back Creek limestone
As above
Qtz
Cal
170a
170
- 2.65
- 6.34
19.9
18.0
- 5.79
4.7
2.6
17.0
17.1
6.5
7.7
Some of the samples contain no workable fluid inclusions, therefore following assumptions have to be made:
a 6lSO fluid data are calculated from mineral data; 613C1 (613 Cmco3) and 613C2 (613 Cnco~) are calculated asssuming fluid with aqueous
species of H2CO3 only and that of HCO 3 only, respectively. Uncertainities in the calculated isotopic composition of the fluid are mainly due
to uncertainties in estimation of the temperature of crystallisation which have a range of _+15~ This would result in an uncertainty in
calculated 6lSOn2o value of about +0.6% at 280~ about +_1.4% at 150~ and uncertainties in calculated 61aCH2co3and 613 CHCO3values
o f less than 0.5%0 and 0.3%0, respectively at temperature between 150~ to 175~
bUsing the Th of DA08, considering the similarities in location and mineralogy between the two samples
cAssuming 40~ below the fluid inclusion measurements from adjacent, early comb quartz or tabular adularia banding, see text f o r
explanation
d Using Th from calcite which coexists with quartz
of ore
minerals
from
Stage
II fluid
220
Mixing of near-neutral, metals-transporting fluid with
cooler, descending acid sulphate fluids or ground water
would also cause metal deposition in response to decreasing temperature, concentrations of chloride and reduced
sulphur. Henley (1991) pointed out that this process is
usually associated with the waning stage of hydrothermal
activity, since a decline of heat supply from the source
regime changes the balance of pressure between hot upflow
(and metal supply) and surrounding (descending) cooler
fluids, and leads to progressive inundation of the system.
The mixing model is unlikely for Stage H mineralisation at
Cracow because Stage I1 is paragenetically old.
Based on exploration of active geothermal systems,
numerous studies (e.g., Browne and Ellis 1970; Browne
1978; Henley 1985; and Hendenquist 1990) showed that
vein adularia, formed due to the fluid becoming more
alkaline, and vein calcite, deposited due to CO2 loss, are
mineralogical indicators of boiling. These observations
were strongly supported by a number of thermodynamic
studies (e.g., Drummond and Ohmoto 1985; Reed and
Spycher 1985; Spycher and Reed 1989; Cathles 1991). The
investigation of the structural state of adularia in epithermal veins (Dong and Morrison 1995), showing relatively
disordered structures, further indicates that vein adularia
was formed under rapid crystallisation conditions which
are most likely induced by boiling of hydrothermal fluids.
In the Cracow district, vein adularia is widespread in
Stage II of all studied vein deposits. Calcite occurs mainly
at Klondyke and Rose's Pride. However, pseudo-acicular
quartz texture, a replacement texture after calcite (Dong et
al. 1995), is often found in Stage II at Central Extended,
indicating the present of calcite precursors. Therefore,
mineralogical and vein textural features suggest that
boiling took place during the Stage I1 mineralisation in all
studied vein deposits.
Many of the effects of boiling on ore deposition have
been computationally modelled and discussed by a number of researchers, including Drummond and Ohmoto
(1985), Reed and Spycher (1985), Seward (1989) and
Cathles (1991). In an example, the evolution of fluid composition has been modelled using the computer program
C H I L L E R (Spycher and Reed 1990). This program is
designed to model boiling, cooling, and various other
chemical interactions in aqueous systems, including solid
and gas phases. The initial fluid composition used in this
calculation is similar to that at the Dawn deposit, which is
in equilibrium with quartz, adularia, albite, illite, chlorite,
pyrite, epidote and calcite at 285 ~ (Dong 1993). Fluid
buffered conditions are assumed during vein formation
because fluids are effectively isolated from wall rocks as
soon as early vein minerals (particularly quartz) precipitate on the walls of fluid conduits.
In most natural systems, when a fluid first boils at deep
levels where permeability is low, very little gas can escape
from the system and the fluid exchanges some heat with
wall rocks (most likely heat is lost through the wall rock,
i.e., subisoenthalpic boiling, cf. Spycher and Reed 1989)
because it flows relatively slowly. However, as the fluid
moves up and encounters an environment of increased
permeability which induces effective gas removal and
a high flow rate, boiling will proceed more vigorously and
heat conduction through wall rocks can be ignored (i.e.,
isoenthalpic boiling). Accordingly, the calculations assume subisoenthalpic boiling (heat loss of 0.8 kcal per
degree C.) in a closed system from 285 ~ to 265 ~ and
followed by isoenthalpic boiling in an open system below
265'~C. The temperature 265~C and the heat loss of
0.8 kcal per degree C. are somewhat arbitrarily chosen,
but this does not matter for the purpose of the exercise
which is mainly for modelling a qualitative trend in the
changes of the solubilities of various species during boiling
of the initial fluid at Cracow. Due to the lack of concentration data for metal species and other aqueous species in
the initial fluid, no attempt is made regarding quantities of
minerals deposited during boiling.
2 ....
7.5
o2
pH
6.5
-3
-4
-2
'
T4~-
-----""''"~
i
:
5.5
"8
HSO4"
-6
0"
-,Ik2-,2~ : . . . . .
-::::
.
=
l
9
9
_-
I
--
....
>.
-6 -
-6 ~
-8
"6
-9
-10
AgCb.-1 1
-5
'
'
-6
s
q0"
-5
" 6 "! ~
,.~.. ~
-7
E
5
-12
1
285
,
265
245
Temperature
~
225
205
(~
221
The results are illustrated in Fig. 5. When sub-isoenthalpic boiling first starts in a closed system, the solubility
of gold is virtually unchanged until about 270 ~ chiefly
because the effect of an increase in pH (stabilising
Au(HS)2 ) overrides that of HzS loss (destabilising
Au(HS)s With further boiling, the effect of H2S degassing becomes more competitive. In addition, when the pH
becomes so high that the dominant sulphide aqueous
species becomes HS-, further increase in pH would have
an opposing effect on gold solubility (i.e. destabilising
Au(HS)2). In this case, gold solubility decreases, especially
when the system is totally open. The solubilities of base
metals invariably drop as the boiling proceeds, mainly in
response to decreasing temperature and increasing pH.
The behaviour of silver depends on the ratio of Ag chloride-complex to Ag bisulphide-complex in the fluid. In the
case of the fluid at Dawn, which shows AgC12greater than
Ag(HS)2, the solubility of total silver drops as boiling
proceeds, similar to that of base metals. In this way,
a metal depth zoning may be developed if the initial fluid
is saturated with respect to Au, Ag and base metals, i.e.
base metal sulphides precipitate immediately after the
fluid boils at deep levels, whereas gold preferentially deposits at shallower levels.
quartz with minor adularia are widely distributed. Replacement textures are distinct, and textures inherited
from silica gel in the upper sections of the deposit give way
to euhedral textures with depth. The mineralisation temperature is determined to be less than 220 ~ and salinity
to be less than 0.18 wt%. Isotopic data indicate nearly
unshifted meteoric water, with 618On2o value of -17% o.
The different characteristics documented above may be
related to several possible factors in epithermal deposits
(Heald et al. 1987). These include:
1. Metal content and mineralogy of the source rock with
respect to the availability of metals for extraction;
2. Chemistry of hydrothermal fluids with respect to their
relative ability to extract, transport, and precipitate metals; and
3. Evolution of the ore-forming hydrothermal system (a)
in time (e.g., different stages of mineralisation) and (b) in
space (e.g., zonation with depth).
As discussed in previous sections, all studied deposits in
the Cracow district are confined to an area of approximately 30 km 2, and are hosted in the Camboon Andesite
which has a massive nature and about 3000 metres in
thickness. Studies of the paragenesis indicate that all deposits experienced essentially the same hydrothermal activities across the camp, and Stage II is a major gold
mineralisation stage. Therefore, differences in the chemistry of the hydrothermal fluids (factor 2) and evolution of
the hydrothermal systems in space (factor 3b) are considered to be the major factors accounting for different
characteristics of Stage II in individual deposits at
Cracow.
The active geothermal systems are considered to be the
archetypes of those systems responsible for epithermal
precious- and base-metal deposits (White 1955, 1981;
Henley and Ellis 1983; Henley 1985). There are three
major end-member fluid types in New Zealand geothermal systems (Hedenquist 1986, 1990). These are: the chloride fluid originating from deeply circulating meteoric
water, and characterised by its high temperature, near
neutral pH, chloride as the dominant anion, a variable
CO2 content, and enriched 6180 with respect to local
meteoric water due to extensive water-rock interaction;
the acid sulphate stream-heated fluid formed by condensation of steam into groundwater near the surface where
H2S is oxidised to sulphate; and the CO2-rich steamheated fluid formed by condensation of steam into nonoxygenated groundwater and characterised by very low
salinity (close to zero) and low temperature (120 to
180 ~ Both steam-heated fluids have isotopic compositions similar to ground water, and generally form an
"umbrella" over the deep chloride upflow.
Many conceptual and descriptive zoning models for
epithermal gold-silver deposits have been proposed (e.g.,
Buchanan 1981; Giles and Nelson 1982; Berger and
Eimon 1982; Henley and Ellis 1983; Sillitoe and Bonham
1984; Silberman and Berger 1985; Heald et al. 1987).
Buchanan (1981) summarised and tabulated data from
over 60 epithermal deposits hosted by volcanic in the
western US, and presented an empirical zoning model
that effectively illustrates the geometric arrangement of
222
Deposits
Ore Zones
Gangue
Quartz textures
Adularia textures
.................................................................................................................................................................
Present surface
Rose's
Pride
&
Klondyke
Precious
metal
Central
Extended
.=~
. ~ . ~ 150 -17.4 pyrite
~'~"
=-o /
~ +hessite
~ ~,~ 220 -16.4 +electrum
~
.~
o
interval
'S
.t-,
Base metal
Dawn
interval
&
quartz
Crustiform,Saccharoidal,
calcite
Pseudo-acicular,
adularia +colloform, +moss, _+comb
laumontile
pyrite
quartz
<210 -13.5 chalcopyrite adularia
sphalerite chlorite
hessite
+sericite
270 -13.0 galena
electrum
Rhombic
Pseudo-acicular
Sub-rhombic
:t:rhombic
pyrite
hessite
+elecmam
(not to scale)
Intrusive
+
+ +
Heat Source
+
..................................................................................................................................................................
Fig. 6. A schematic zoning model for Stage II mineralisation in the Cracow hydrothermal system
changing conditions also account for the common presence of coarse comb quartz texture and sub-rhombic
adularia variety. The deep position in the system allows
extensive water-rock isotopic exchange to take place and
prevents the participation of fresh meteoric water, thus the
6180 values of the fluid were shifted from palaeo-meteoric
water to as high as -12Too at Dawn.
The formation of orebodies at Central Extended is
perhaps a good example of extensive boiling at shallow
levels. Here isoenthalpic boiling took place in an open
system. The rapid loss of volatile components and cooling
led to a sharp decrease in gold solubility, with essentially
all of the gold being deposited over a narrow depth
interval. The rapidly changing conditions also account for
the common presence of micro-rhombic adularia and
widespread quartz textures possibly inherited from silica
gel. Conventionally, there should be a deeper zone rich in
base metal sulphides. However, if the initial fluid was
dilute and therefore could only carry limited amounts of
base metals, or the initial fluid was substantially undersaturated with respect to base metals, a base-metal sulphide-rich zone may not be developed at depth.
CO2-rich-steam-heated fluid is considered to have been
predominated in the upper parts of the systems as represented at Rose's Pride and Klondyke. Heating of this
CO2-rich steam-heated fluid will lead to precipitation of
calcite due to its inverse solubility. However, this process
cannot account for the coexistence of calcite, adularia and
quartz-the mineral assemblage commonly observed at
Rose's Pride and Klondyke, because both the solubility of
quartz and the AI(OH)2 stability increase with increasing
223
temperatures which results in a fluid undersaturated with
respect to quartz and adularia. On the other hand, boiling
of the CO2-rich steam-heated fluid, resulting in loss of
CO2, cooling, enrichment of solutes and increase in pH, is
a better mechanism of mineral deposition at Rose's Pride
and Klondyke. The low temperature and low salinity of
the fluid preclude the transport of base metal complexes,
hence base metal sulphides are virtually absent at Rose's
Pride and Klondyke. As indicated by Hedenquist (1986
and 1990), the mixed-layer illite-smectite along with minor
kaolinite is consistent with the presence of COz-rich
steam-heated waters at shallow levels in New Zealand
geothermal systems. However, from the examination of
available samples and drill core logs, these minerals
are only present in minor amounts at Rose's Pride and
Klondyke thus indicating that the argillic alteration
was not well developed in association with Stage II mineralisation at these deposits. A possible explanation is that
the CO2-rich steam-heated fluid underwent boiling soon
after condensation of the steams into groundwater, shifting mineral-fluid equilibria back to K-feldspar stability
field.
Conclusions
References
224
Henley, R.W., Ellis, A.J. (1983) Geothermal systems, ancient and
modern: a geochemical review. Earth Sci. Rev. 19 : 1 -50
McCrae, J.M. (1950) On the isotope chemistry of carbonates and
a paleotemperature scale. J. Chem. Phys. 18:849 857
Morrison, G.W,, Dong, G., Jaireth, S. (1990) Textural zoning in
epithermal quartz veins. Epithermal and porphyry style gold
deposits in Queensland. Unpublished field manual, AMIRA project p247, Australian Mineral Industries Research Association
Limited, 19 pp
Ohmoto, H., Rye, R.O. (1979) Isotope of sulfur and carbon: In
Barnes, H.L. (ed) Geochemistry of hydrothermal ore deposits,
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