23.03.2013 Views

Session 5 Epigenetic gold systems - Extra Materials - Springer

Session 5 Epigenetic gold systems - Extra Materials - Springer

Session 5 Epigenetic gold systems - Extra Materials - Springer

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

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 />

555

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!