Session 5 Epigenetic gold systems - Extra Materials - Springer
Session 5 Epigenetic gold systems - Extra Materials - Springer
Session 5 Epigenetic gold systems - Extra Materials - Springer
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dition to CO 2 may contain up to 10 % N 2 . The early event<br />
of grey quartz crystallization corresponds to auriferous<br />
arsenopyrite and pyrite precipitation.<br />
The second generation of quartz of white colour that<br />
forms veinlets and rock matrix seems to be related to pyrite<br />
and base-metals sulphides precipitation also associated<br />
with crystallization of carbonates of various compositions<br />
(mainly ankerite). This quartz crystallized within<br />
the temperature ranges from 273 to 244 ° C with the salinity<br />
of fluids of 8.5 to 6.4 wt % NaCl equivalent and at<br />
pressure of 0.7 kb. The contents of salts in comparison to<br />
the inclusion solution composition in grey quartz are characterized<br />
here by higher NaCl contents up to 85% and<br />
lower content of KCl, CaCl 2 and AlCl 3 (Fig. 2). In the sample<br />
richest in <strong>gold</strong> (>60 ppm Au) FeCl 3 appears in the amount<br />
up to 5% of total salts. Furthermore, in two-phase aqueous<br />
fluid inclusions beside CO 2 methane appears commonly<br />
(up to 10% CH 4 ). The third generation of quartz<br />
crystallized from 200 to 180 0 C with salinity of fluids about<br />
4.5 of wt % NaCl equivalent and pressure at 0.7 kb. The<br />
salts in inclusion fluids are dominated by NaCl (92-97 %<br />
of total salts) and low contents of CaCl 2 (3-7 % of total<br />
salts). The lowest crystallization temperatures from 165<br />
to 154 ° C are measured in quartz veinlets of the next generation.<br />
Fluid inclusions in that quartz homogenized into<br />
the liquid phase and are characterized by presence of NaCl<br />
dissolved in water, exclusively. The data in Fig. 1 shows a<br />
clear linear trend, due to hypothetical dilution by formation<br />
waters?<br />
5 Sulphur isotope in sulphides from Klecza<br />
The sulphur isotope compositions (δ 34 S CDT) have been<br />
determined in several pure sulphide samples from the<br />
Klecza area. Contents of sulphur δ 34 S CDT in mediumand<br />
fine-grained arsenopyrite from Klecza range from<br />
+2.25 to +7.88 ‰ δ 34 S and in coarse-grained pyrite they<br />
are from –1.62 to –1.49 ‰ δ 34 S. The values of the sulphur<br />
isotope compositions of the considered sulphides reflect<br />
a sulphur contribution from the host rocks beside the<br />
magmatic input of sulphur into mineralizing fluids during<br />
precipitation of the sulphides. However, there is no<br />
direct evidence of magmatism in the surrounding area.<br />
Especially, samples of massive arsenopyrite aggregates<br />
hosted by a quartz vein in chlorite-sericite schists have<br />
heavier sulphur isotope compositions (up to 7.88 ‰) that<br />
indicate for sulphur contribution from the host rocks.<br />
6 Discussion and conclusions<br />
Chapter 5-9 · Fluid inclusion study of quartz veins from the orogenic Klecza <strong>gold</strong> deposit in the Kaczawa Mountains (SW Poland)<br />
Primary fluid inclusions in different generations of auriferous<br />
quartz from rock samples from the Klecza <strong>gold</strong><br />
deposit revealed the presence of moderate to low saline<br />
two-phase aqueous fluids with CO 2 , N 2 and CH 4 . Reported<br />
crystallization temperatures for the refractory sulphide-<br />
bearing grey quartz ranges from 340 to 284 ° C with the<br />
salinity of fluids of 12.3 to 9.2 wt% NaCl equivalent and<br />
pressure of 0.9 kb. The white quartz associated with nonrefractory<br />
<strong>gold</strong>, base metal sulphides, and carbonates crystallized<br />
at temperatures range from 273-244 ° C with the<br />
salinity of fluids of 8.5 to 6.4 wt % NaCl equivalent and at<br />
pressure of 0.7 kb. The features of fluid inclusions in <strong>gold</strong>bearing<br />
quartz were considered by Kozlowski and Metz<br />
(1989). They are: temperatures 250-350 ° C, pressure 0.4-1<br />
kbar, abundance of CO2 , especially hetero-genisation<br />
(splitting of the one phase medium into two- or morephase<br />
medium) of aqueous and carbon dioxide fluids<br />
(Popivnyak 1975), methane in the ore-forming fluids<br />
(Kalyuzhnyi et al. 1975) and presence of other than sodium<br />
cations in fluids, especially high contents of K and<br />
occurrence of Al, Ca, and Fe in <strong>gold</strong>-precipitating solutions,<br />
and strong domination of Na in pre- and post-ore<br />
fluids.<br />
These features were recognized in fluid inclusions in<br />
quartz of the studied deposit. The changes of the oreforming<br />
solution like separation of carbon dioxide and<br />
aqueous fluids, replacement of sodium by potassium and<br />
other ions and presence of methane influencing the oxygen<br />
fugacity may cause the instability of the <strong>gold</strong>-transporting<br />
chloride, carbonate or bisulphide complexes, leading<br />
to precipitation of native <strong>gold</strong>. Gold mineralization<br />
zones are hosted in quartz ± sericite ± graphitic schists.<br />
Common presence of organic matter and graphite has<br />
been recognized in the studied samples from Klecza. Contents<br />
of TOC (Total Organic Carbon) range from traces<br />
up to 18.7 %. Graphitic schists horizons are common in<br />
the Pilchowice unit and formed during recrystallization<br />
and redistribution of carbon in metamorphosed black<br />
argillites. Carbon present in the country rocks reacted<br />
with water from fluids to produce carbon dioxide and<br />
methane according to reaction: 2C + 2H2O = CO2 + CH4 .<br />
In this study methane was always measured in fluid inclusions<br />
(up to 10 %) in the most auriferous samples. Presence<br />
of methane causes reduction of the oxygen fugacity<br />
and destabilizes <strong>gold</strong> complex inducing <strong>gold</strong> precipitation<br />
(Cox et al. 1991). Graphitic schists with their reducing<br />
character, acted as preferential site for <strong>gold</strong> precipitation.<br />
The correlation between <strong>gold</strong> and sulphur as well as<br />
common occurrence of <strong>gold</strong> inclusions in pyrite and arsenopyrite<br />
of the first ore stage mineralization suggest<br />
that <strong>gold</strong> was transported as reduced bisulphide complexes<br />
[Au (HS) - 2 ] during this stage of ore precipitation. However,<br />
the composition of fluid inclusions indicates also<br />
for chloride complexes as <strong>gold</strong> transporting during next<br />
stages of Au precipitation.<br />
The role of nitrogen in the fluids is not obvious. It may<br />
come either from the decomposing organic matter or from<br />
dissolved potassium feldspars or micas, where it may be<br />
present in form of ammonia ions. In any of the abovelisted<br />
cases it may migrate into the system together with<br />
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