Element transport and enrichment during propylitic alteration in Paleozoic porphyry Cu mineralization systems: Insights from chlorite chemistry

2018 ◽  
Vol 102 ◽  
pp. 437-448 ◽  
Author(s):  
Bing Xiao ◽  
Huayong Chen ◽  
Pete Hollings ◽  
Yunfeng Wang ◽  
Juntao Yang ◽  
...  
2020 ◽  
Vol 115 (4) ◽  
pp. 871-901 ◽  
Author(s):  
Kevin Byrne ◽  
Guillaume Lesage ◽  
Sarah A. Gleeson ◽  
Stephen J. Piercey ◽  
Philip Lypaczewski ◽  
...  

Abstract The Highland Valley Copper porphyry deposits, hosted in the Late Triassic Guichon Creek batholith in the Canadian Cordillera, are unusual in that some of them formed at depths of at least 4 to 5 km in cogenetic host rocks. Enrichments in ore and pathfinder elements are generally limited to a few hundred meters beyond the pit areas, and the peripheral alteration is restricted to narrow (1–3 cm) halos around a low density of prehnite and/or epidote veinlets. It is, therefore, challenging to recognize the alteration footprint peripheral to the porphyry Cu systems. Here, we document a workflow to maximize the use of lithogeochemical data in measuring changes in mineralogy and material transfer related to porphyry formation by linking whole-rock analyses to observed alteration mineralogy at the hand specimen and deposit scale. Alteration facies and domains were determined from mapping, feldspar staining, and shortwave infrared imaging and include (1) K-feldspar halos (potassic alteration), (2) epidote veins with K-feldspar–destructive albite halos (sodic-calcic alteration), (3) quartz and coarse-grained muscovite veins and halos and fine-grained white-mica–chlorite veins and halos (white-mica–chlorite alteration), and two subfacies of propylitic alteration comprising (4) prehnite veinlets with white-mica–chlorite-prehnite halos, and (5) veins of epidote ± prehnite with halos of chlorite and patchy K-feldspar. Well-developed, feldspar-destructive, white-mica alteration is indicated by (2[Ca-C] + N + K)/Al values <0.85, depletion in CaO and Na2O, enrichment in K2O, and localized SiO2 addition and is spatially limited to within ~200 m of porphyry Cu mineralization. Localized K2O, Fe2O3, and depletion in Cu, and some enrichment in Na2O and CaO, occurs in sodic-calcic domains that form a large (~34 km2) nonconcentric footprint outboard of well-mineralized and proximal zones enriched in K. Water and magmatic CO2-rich propylitic and sodic-calcic–altered rocks form the largest lithogeochemical footprint to the mineralization in the Highland Valley Copper district (~60 km2). Calcite in the footprint is interpreted to have formed via phase separation of CO2 from a late-stage magmatic volatile phase. Several observations from this study are transferable to other porphyry systems and have implications for porphyry Cu exploration. Feldspar staining and shortwave infrared imaging highlight weak and cryptic alteration that did not cause sufficient material transfer to be confidently distinguished from protolith lithogeochemical compositions. Prehnite can be a key mineral phase in propylitic alteration related to porphyry genesis, and its presence can be predicted based on host-rock composition. Sodic-calcic alteration depletes the protolith in Fe (and magnetite) and, therefore, will impact petrophysical and geophysical characteristics of the system. Whole-rock loss on ignition and C and S analyses can be used to map enrichment in water and CO2 in altered rocks, and together these form a large porphyry footprint that extends beyond domains of enrichment in ore and pathfinder elements and of pronounced alkali metasomatism.


2021 ◽  
Vol 11 (2) ◽  
pp. 479
Author(s):  
Christos L. Stergiou ◽  
Vasilios Melfos ◽  
Panagiotis Voudouris ◽  
Paul G. Spry ◽  
Lambrini Papadopoulou ◽  
...  

The Vathi porphyry Cu-Au ± Mo mineralization is located in the Serbo-Macedonian metallogenic province of the Western Tethyan Metallogenic Belt. It is mainly hosted by a latite and is genetically associated with a quartz monzonite intrusion, which intruded the basement rocks of the Vertiskos Unit and the latite, 18 to 17 Ma ago. A phreatic breccia crosscuts the latite. The quartz monzonite was affected by potassic alteration, whereas the latite was subjected to local propylitic alteration. Both styles of alteration were subsequently overprinted by intense sericitic alteration. M-type and A-type veins are spatially associated with potassic alteration, whereas D-type veins are related to the sericitic alteration. Three ore assemblages are associated with the porphyry stage: (1) pyrite + chalcopyrite + bornite + molybdenite + magnetite associated with potassic alteration; (2) pyrite + chalcopyrite related to propylitic alteration; and (3) pyrite + chalcopyrite + native gold ± tetradymite associated with sericitic alteration. A fourth assemblage consisting of sphalerite + galena + arsenopyrite + pyrrhotite + pyrite ± stibnite ± tennantite is related to an epithermal overprint. Fluid inclusion data indicate that the A-type veins and related porphyry-style mineralization formed at 390–540 °C and pressures of up to 646 bars (<2.6 km depth) from boiling hydrothermal fluids. A later condensation of vapor-rich inclusions resulted in a moderately saline fluid (8.4–11.2 wt % NaCl equiv) at temperatures between 311 and 392 °C, which were related to sericitic alteration, D-type veins, and associated metallic mineralization. Subsequent dilution of the moderately saline fluid at lower temperatures (205–259 °C) produced a less saline (1.4–2.9 wt % NaCl equiv.) fluid, which is likely associated with the late epithermal overprint.


2020 ◽  
Vol 115 (4) ◽  
pp. 729-748 ◽  
Author(s):  
Adam Pacey ◽  
Jamie J. Wilkinson ◽  
Adrian J. Boyce ◽  
Ian L. Millar

Abstract In porphyry ore deposit models, the propylitic alteration facies is widely interpreted to be caused by convective circulation of meteoric waters. However, recent field-based and geochemical data suggest that magmatic-derived fluids are likely to contribute to development of the propylitic assemblage. In order to test this hypothesis, we determined the oxygen and hydrogen isotope compositions of propylitic mineral separates (epidote, chlorite, and quartz), selected potassic mineral separates (quartz and magnetite), and quartz-hosted fluid inclusions from around the E48 and E26 deposits in the Northparkes porphyry Cu-Au district, New South Wales, Australia. In addition, the strontium isotope composition of epidote was determined to test for the potential contribution of seawater in the Northparkes system given the postulated island-arc setting and submarine character of some country rocks. Oxygen isotope geothermometry calculations indicate potassic alteration occurred between ~600° and 700°C in magmatic/mineralized centers, persisting to ~450°C upon lateral transition into propylitic alteration. Across the propylitic facies, temperature progressively decreased outward to &lt;250°C. These temperature estimates and additional data from chlorite geothermometry were utilized to calculate the oxygen and hydrogen isotope composition of the fluid in equilibrium with the sampled minerals. Results show that propylitic fluids spanned a range of compositions with δ18O between 0.5 and 3.7‰ and δD between –49 and –17‰. Comparison of these results with the modeled compositions of meteoric and/or magmatic fluids during their evolution and isotopic exchange with local country rocks shows that a magmatic fluid component must exist across the propylitic halo during its formation. Strontium isotope data from propylitic epidote provide initial (based on formation at ~450 Ma) 87Sr/86Sr values in the range of 0.704099 to 0.704354, ruling out the presence of seawater as a second fluid in the system. Although we cannot exclude magmatic-meteoric mixing, especially toward the fringes of the system, our results support a model in which magmatic-derived fluid is the primary driver of propylitic alteration as it undergoes cooling and chemical equilibration during outward infiltration into country rocks. This is consistent with chemical mass transfer calculations for Northparkes and published chemical-thermodynamic models that only require a magmatic fluid for the production of propylitic assemblages. In view of this and supporting data from other deposits, we suggest that magmatic fluids are essential drivers of propylitic alteration in porphyry systems.


2020 ◽  
pp. SP502-2019-139
Author(s):  
Mallam Mamane Hallarou ◽  
Moussa Konaté ◽  
Akinade Shadrach Olatunji ◽  
Yacouba Ahmed

AbstractThe Kourki porphyry Cu–Mo deposit is located in the southern part of the Gorouol greenstone belt in Western Niger. The potential Cu–Mo mineralization is hosted by granitoids (granodiorite and diorite) and veins, in Paleoproterozoic plutonic rocks, which are the main porphyry Cu–Mo system. The scientific objective of this study was to determine the characteristics of Kourki Cu–Mo mineralization and to compare them with other porphyry systems in the world and particularly with those of the West African Craton. The methods implemented consist of a field study and a polarizing microscope analysis in transmitted and reflected light on the rocks bearing Cu–Mo mineralization. The use of reference diagrams made it possible, on the one hand, to confirm the origin of the Cu–Mo mineralization and, on the other hand, to specify conditions of the formation of this mineralization. The geology of the study area shows a granodiorite–tonalite pluton in close contact with dioritic intrusions to the north, clastic sediments to the east, and volcano-sedimentary rocks to the SE. The pluton is crosscut by an intrusion of molybdenum porphyry dyke with irregular shape that can be observed in outcrop. The geochemical study shows that the granodiorite–tonalite pluton can be related to a calc-alkaline plutonic series which characterizes an arc type environment. Large areas of hydrothermal quartz breccia have been identified within the pluton. They were set up by hydraulic fracturing along the zones of weakness. Most of the Cu–Mo mineralization in the Kourki deposit occurs as hydrothermal breccia, filled with veins, and was disseminated in the porphyry diorite and quartz–diorite stockworks. The mineralogical assemblage is marked by a predominance of pyrite, molybdenite, chalcopyrite and quartz with some bornite and chalcocite. The alterations include potassic alteration, propylitic alteration, sericitization and epidotization. All of these data show that the Kourki porphyry represents a characteristic system of an environmental arc, quite comparable with that of the Andean Cordillera.


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