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Exploration for porphyry-style copper mineralisation near Llandeloy

Exploration for porphyry-style copper mineralisation near Llandeloy

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increase the Zr content. The division between tonalites<br />

and diorites is clearly defined and two trends are evident<br />

in the diorites which merge in the tonalite field. One<br />

trend, characterised by low Mg/Zr and Ti/Zr is <strong>for</strong>med<br />

by the microdiorite and quartz microdiorite samples<br />

from borehole 7 (Fig. 33). The higher trend is followed by<br />

ail other diorite samples and these contain distinctly<br />

higher Mg/Zr and Ti/Zr ratios. The only samples which<br />

faU off-line are highly rnineralised and contain a high<br />

proportion of quartz or carbonate vein material. The<br />

distinctive 'immobilet element content of the lower<br />

Mg/Zr group, particularly the quartz microdiorites from<br />

borehole 7, suggests a genetic difference but in borehole<br />

4 quartz diorite from the high Mg/Zr group intrudes a<br />

microdiorite complex that contains rocks from both<br />

trends, porphyritic microdiorite passing imperceptibly<br />

into microdiorite. Another feature, and an apparent<br />

paradox of the intrusives, is that the sequence of<br />

intrusion based on contact relationships is almost the<br />

reverse of that which might be predicted on a simplistic<br />

igneous differentiation model. It is not thought possible<br />

to resolve these problems with the data available and it<br />

is simply concluded that the petrogenesis of these<br />

intrusives is probably a complex multiphase event.<br />

The chemical co mpition of the intrusive rocks<br />

indicates their affinity with intrusions emplaced in an<br />

island arc setting. Examination of the least altered rocks<br />

SuEXests that CaO = Na2O + K20 at 56057% SiO2, giving<br />

them a calc-alkali composition. Very low Nb contents,<br />

maximum 7 ppm, suggest an island arc rather than<br />

continental margin setting. All samples plot in the low-<br />

Rb volcanic-arc field of the Nb v SiOz plot of Pearce<br />

and Gale (1977). The low K, Rb, Ba, Sr, Th and Zr<br />

content of the least altered rocks and high K/Rb ratios<br />

(mean = 383 <strong>for</strong> 39 intrusives) compared with<br />

comparative lithologies emplaced in a continental<br />

margin setting (e.g. Saunders, Tarney and Weaver, 1979)<br />

is consistent with this conclusion.<br />

Alteration associated with dbmina ted <strong>copper</strong><br />

mineralisat ion Chemical ' changes accompanying alteration<br />

proved difficult to study because of the variety of<br />

rock types, the lack of unaltered rocks <strong>for</strong> comparison<br />

and the complex series of alteration events. Only major<br />

chem ical changes accompanying a1 tera t ion have been<br />

determined in this study, and a more rigerous<br />

investigation is required involving further careful<br />

Figure 34 Plot of K v Rb, showing the effects of potassic alteration<br />

sampling, analysis and mineralogical studies to clarify<br />

the chemieal signatures of the various alteration events.<br />

For the purpose of this study four major alteration<br />

episodes are distinguished: (i) weathering, (ii) alteration<br />

and metasomatism on a regional scale, possibly<br />

associated with bw grade metamorphism, (iii) alteration<br />

associated with disseminated <strong>copper</strong> <strong>mineralisation</strong> and<br />

(iv) localised alter8 t ion associated with vein<br />

minerallsation. Any regional me taso matism can be<br />

expected to affect all the samples whilst weathering<br />

effects are evident in surface and <strong>near</strong> surface samples.<br />

The process dominant in the borehole samples is<br />

alteration associated with the targeted disseminated<br />

<strong>copper</strong> <strong>mineralisation</strong>, Here only alteration affecting<br />

borehole samples is considered and, because major<br />

elements were only determined on fresh igneous rock<br />

samples, principally alteration affecting the intrusive<br />

rocks.<br />

Chemical studies about well documented <strong>porphyry</strong><br />

<strong>copper</strong> deposits ,such as Highland Valley, British<br />

Columbia (Olade and Fletcher, 1976; Olade, 1977),<br />

Bougainville (Ford, 1978) and northern Turkey (Taylor<br />

and Fryer, 1980) have indicated that most elements can<br />

be at least locally redistributed in the alteration zones<br />

farmed by a W r <strong>porphyry</strong> system. It is not surprising,<br />

there<strong>for</strong>e, that compatible element ratios, plots of socalled<br />

immobile elements and mobile/immobile element<br />

ratios in igneous rocks against well documented igneous<br />

rock trends (eg. Beswick and Soucie, 1978; Davies and<br />

others, 19791, show that <strong>near</strong>ly all the elements<br />

determined in <strong>Llandeloy</strong> borehole samples show some<br />

evidence of at least limited redistribution attributable to<br />

alteration processes. At <strong>Llandeloy</strong> the situation is<br />

complicated by the late stage propylitic overprinting of<br />

earlier alteration and only rocks containing remnant K-<br />

feldspar alteration yield a distinctive geochemical<br />

signature.<br />

Few analysed samples contain remnant K-feldspar but<br />

in boreholes 2 (quartz microdiorite) and 5 (tonalite) this<br />

and weaker <strong>for</strong>ms of alteration are present within the<br />

same lithology, allowing a comparison to be made<br />

without the complication of major host rock variation.<br />

The comparison shows that K-feldspar alteration is<br />

characterised by great increases in K20 and small<br />

increases in Rb (Fig. 34). CaO, Sr and Na decrease whilst<br />

Ba shows erratic behaviour decreasing in K-feldspar<br />

bearing rocks in these two boreholes but elsewhere<br />

o Samples showing K-fe1d.p.r alteration<br />

A Sampka from surface exposums<br />

0 Samplaa of gum nncrodion~m from 8H 2<br />

rhormng biottn alteration

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