Remote sensing, SWIR, Raman and XRD applications in Pesovets epithermal system mapping, Panagyurishte ore district, Bulgaria

Remote sensing UAV based study combined with field mapping, SWIR, XRD Raman and XRF tests for mineral detection outlined advanced argillic alteration domains in the Pesovets silica cap to demonstrate quick approach for epithermal gold exploration targeting and evaluation. As and Ti increasing trend toward epithermal high-sulphidation Cu-Au mineralization could be employed as a proximal path finder.

Exploring magmatic gas and subvolcanic hydrothermal system interactions: Mineralogy and sulfur isotope characteristics of the Holocene volcanic products at Mt. Tangkuban Parahu, Indonesia.

A subvolcanic-hydrothermal system involves complex interaction between magma, magmatic fluids, and hydrothermal system at stratovolcanoes in subduction setting. These interactions are responsible for magmatic-hydrothermal eruption associated with rapid injection of magmatic gas into hydrothermal system at a certain depth of volcanic edifice. However, capturing these interactions is challenging due to inaccessibility to the crater conduit within the edifice. Therefore, we selected a method to analyze the volcanic products from several episodic phreatic and phreatomagmatic eruptions during the Holocene at Tangkuban Parahu, Indonesia. In this context, Holocene volcanic products are one of the best examples to understand an interplay between magma, magmatic fluids, and hydrothermal system in producing violent eruptions. In this study, we carried out petrological and sulfur isotope analysis only for the hydrothermally altered lithic ash particles, a part of proximal volcanic products. Mineral assemblages mostly exhibit a typical acid-sulfate and advanced argillic alteration, consisting of alunite, kaolinite, and silica minerals. Acid-sulfate and advanced argillic alteration indicates that those mineral assemblages were formed under the formation temperature ranging from ~100 to ~260 . The calculated temperature from sulfur isotopic fractionation of sulfate-sulfide shows 230-240 , which is almost identical with assigned temperature from mineral assemblages. Sulfur isotope and jarosite occurrence indicate the supergene alteration associated with oxygen entrainment to the hydrothermal system that oxidize pyrite to jarosite. Sulfur isotopic variation throughout the studied stratigraphy represents influx of magmatic gas to the hydrothermal system. Moreover, zoned P-bearing alunite represents repetitive injection of magmatic gas to the active acidic hydrothermal system, which also indicates the magmatic-hydrothermal interaction below the crater. Occurrence of enargite and chalcopyrite represents the nature of upper-level high sulfidation system at shallow volcanic edifice of the Tangkuban Parahu volcano. Furthermore, we showed that coupled petrological and sulfur isotope analysis has paramount importance to evaluate the conditions of the subvolcanic hydrothermal system, magmatic-hydrothermal interaction, and the origin of steam-blast eruptions at volcanoes that contain subvolcanic-hydrothermal systems.

The Pliocene Ixtacamaxtitlán low sulfidation epithermal deposit (Puebla, Mexico): A case of fossil fungi consortia in a steam-heated environment

The Ixtacamaxtitlán area in northern Puebla (central Mexico) contains middle Miocene Cu-Mo-Au porphyry/skarn and Pliocene low-sulfidation Au-Ag epithermal deposits that are geologically associated with the evolution of the Trans-Mexican Volcanic Belt (TMVB). In this paper, a new 40Ar/39Ar age (2.87 ± 0.41 Ma) is provided for rhombohedral alunite from a kaolinite + alunite ± opal ± cristobalite ± smectite advanced argillic alteration assemblage. This age contributes to the definition of a metallogenic province that is confined to the TMVB, a relevant feature for regional exploration. A ~12 My gap is established between the formation of the Cu-Mo-Au porphyry/skarn and low-sulfidation Au-Ag epithermal deposits, which rules out the possibility that their overlapping was the result of telescoping. Advanced argillic alteration is conspicuous throughout the mineralized area. This alteration assemblage consists of a widespread kaolinite-rich blanket that underlies silica sinters, polymictic hydrothermal breccias, and an alunite-rich spongy layer that consists of vertical tubular structures that are interpreted as the result of gas venting in a subaerial environment. The above indicate a shallow hypogene origin for the advanced argillic alteration assemblage—that is, formation by the partial condensation within a phreatic paleoaquifer of acidic vapors that were boiled-off along fractures that host epithermal veins at depth. The formation of the spongy alunite layer and silica sinters is interpreted to have been synchronous. Within the alunite-rich spongy layer, tubular structures hosted microbial consortia dominated by fungi and possible prokaryote (Bacteria or Archaea) biofilms. Such consortia were developed on previously formed alunite and kaolinite and were preserved due to their replacement by opal, kaolinite, or alunite. This means that the proliferation of fungi and prokaryotes occurred during a lull in acidic gas venting during which other organisms (i.e., algae) might have also prospered. Periodic acidic gas venting is compatible with a multi-stage hydrothermal system with several boiling episodes, a feature typical of active geothermal systems and of low-sulfidation epithermal deposits. The microstructures, typical for fungi, are mycelia, hyphae with septa, anastomoses between branches, and cord-like groupings of hyphae. Possible evidence for skeletal remains of prokaryote biofilms is constituted by cobweb-like microstructures composed of <1 µm thick interwoven filaments in close association with hyphae (about 2.5 µm thick). Bioweathering of previously precipitated minerals is shown by penetrative biobrecciation due to extensive dissolution of kaolinite by mycelia and by dissolution grooves from hyphae on alunite surfaces. Such bioweathering was possibly predated by inorganically driven partial dissolution of alunite, which suggests a lull in acidic gas venting that allowed living organisms to thrive. This interpretation is sustained by the occurrence of geometrical dissolution pits in alunite covered by hyphae. Fungal bioweathering is particularly aggressive on kaolinite due to its relatively poor nutrient potential. Such delicate microstructures are not commonly preserved in the geological record. In addition, numerous chalcopyrite microcrystals or microaggregates are found within the alunite layer, which could be related to sulfate reduction due to bacterial activity from the sulfate previously released by fungal bioweathering of alunite. Hydrogeochemical modeling constrains pH to between ~3.2 and ~3.6 and temperature to between 53 and 75 °C during the stage in which fungi and other organisms thrived. These waters were cooler and more alkaline than in earlier and later stages, which were characterized dominantly by steam-heated waters. The most likely process to account for this interlude would be mixing with meteoric water or with upwelling mature water that did not undergo boiling.

The Onto Cu-Au Discovery, Eastern Sumbawa, Indonesia: A Large, Middle Pleistocene Lithocap-Hosted High-Sulfidation Covellite-Pyrite Porphyry Deposit

In 2013, a diamond drill program tested an extensive advanced argillic alteration lithocap within the Hu’u project on eastern Sumbawa Island, Indonesia. A very large and blind copper-gold deposit (Onto) was discovered, in which copper occurs largely as disseminated covellite with pyrite, and as pyrite-covellite veinlets in a tabular block measuring at least 1.5 × 1 km, with a vertical thickness of ≥1 km. Copper and gold are spatially related with a series of coalesced porphyry stocks that intrude a polymictic diatreme breccia capped by a sequence of intramaar laminated siltstones, volcaniclastic and pyroclastic rocks, and overlain by andesite flows and domes. The porphyry intrusions were emplaced at shallow depth (≤1.3 km), with A-B–type quartz veinlet stockworks developed over a vertical interval of 300 to 400 m between ~100 and 500 m below sea level (bsl), 600 to 1,000 m below the present surface, which is at 400 to 600 m above sea level. In the area drilled at Onto, the diatreme breccia, all porphyry intrusions and, to a lesser extent, the surrounding older andesite sequence have all been overprinted by intense subhorizontal advanced argillic alteration, zoned downward from illite-smectite, quartz-dickite to quartz-alunite and quartz-pyrophyllite ± diaspore alteration. The alteration package includes two particularly well-developed zones of residual quartz with vuggy texture in subhorizontal zones at shallow depth, the upper one is still porous but the lower horizon, ~100 m thick, is largely silicified and is located at or near the top of the quartz-alunite alteration. Mineralization starts below the lowermost silicic horizon with more than 90% of the current resource in quartz-pyrophyllite-alunite and quartz-alunite alteration. Mineralization is dominated by a high-sulfidation assemblage of covellite-pyrite ± native sulfur largely in open-space fillings and replacements, but also as discrete pyrite-covellite and covellite only veins down to at least 1 km. Although the greatest amount of copper occurs as paragenetically late covellite deposited during formation of the advanced argillic alteration, approximately 60% of resource at 0.3% Cu cutoff still occurs within the porphyry stocks, indicating the porphyry stocks are a fundamental control on mineralization. There is considerable remobilization and dispersion of copper and, to a lesser extent, gold into the surrounding pre-mineral breccia and the late intermineral intrusions from the two earliest porphyry phases, resulting in quite consistent copper and gold grades throughout the currently delineated mineral resource. The very high sulfidation state of the mineralization is thought to be a consequence of the metal-bearing ore fluids cooling in the advanced argillic-altered host rocks in the absence of a rock buffer. Early chalcopyrite-bornite ± pyrite mineralization with potassic ± chloritic and sericitic alteration is only preserved on the margins of the system and more rarely at depth in a few holes 600 m bsl (~1,100 m below surface) but makes up only a small proportion (~8%) of the current resource. The Onto system is exceptionally young and formed rapidly in the middle Pleistocene and is not significantly eroded. A U-Pb zircon age for the andesite that caps the volcanosedimentary host rocks provides a maximum age of 0.838 ± 0.039 Ma, with a slightly younger porphyry zircon crystallization age of 0.688 ± 0.053 Ma. Re-Os dating of molybdenite that is associated with both the quartz vein stockwork and high-sulfidation assemblage copper mineralization shows overlap between 0.44 ± 0.02 and 0.35 ± 0.0011 Ma. 40Ar/39Ar ages for alunite within the advanced argillic alteration block ranges from 0.98 ± 0.22 to 0.284 ± 0.080 Ma, and alunite closely associated with covellite spans a period from 0.537 ± 0.064 to 0.038 ± 0.018 Ma.

Reconstruction of an Early Permian, Sublacustrine Magmatic-Hydrothermal System: Mount Carlton Epithermal Au-Ag-Cu Deposit, Northeastern Australia

The Mt. Carlton Au-Ag-Cu deposit, northern Bowen basin, northeastern Australia, is an uncommon example of a sublacustrine hydrothermal system containing economic high-sulfidation epithermal mineralization. The deposit formed in the early Permian and comprises vein- and hydrothermal breccia-hosted Au-Cu mineralization within a massive rhyodacite porphyry (V2 open pit) and stratabound Ag-barite mineralization within volcano-lacustrine sedimentary rocks (A39 open pit). These orebodies are all associated with extensive advanced argillic alteration of the volcanic host rocks. Stable isotope data for disseminated alunite (δ34S = 6.3–29.2‰; δ18OSO4 = –0.1 to 9.8‰; δ18OOH = –15.3 to –3.4‰; δD = –102 to –79‰) and pyrite (δ34S = –8.8 to –2.7‰), and void-filling anhydrite (δ34S = 17.2–19.2‰; δ18OSO4 = 1.8–5.7‰), suggest that early advanced argillic alteration formed within a magmatic-hydrothermal system. The ascending magmatic vapor (δ34SΣS ≈ –1.3‰) was absorbed by meteoric water (~50–60% meteoric component), producing an acidic (pH ≈ 1) condensate that formed a silicic → quartz-alunite → quartz-dickite-kaolinite zoned alteration halo with increasing distance from feeder structures. The oxygen and hydrogen isotope compositions of alunite-forming fluids at Mt. Carlton are lighter than those documented at similar deposits elsewhere, probably due to the high paleolatitude (~S60°) of northeastern Australia in the early Permian. Veins of coarse-grained, banded plumose alunite (δ34S = 0.4– 7.0‰; δ18OSO4 = 2.3–6.0‰; δ18OOH = –10.3 to –2.9‰; δD = –106 to –93‰) formed within feeder structures during the final stages of advanced argillic alteration. Epithermal mineralization was deposited subsequently, initially as fracture- and fissure-filling, Au-Cu–rich assemblages within feeder structures at depth. As the mineralizing fluids discharged into lakes, they produced syngenetic Ag-barite ore. Isotope data for ore-related sulfides and sulfosalts (δ34S = –15.0 to –3.0‰) and barite (δ34S = 22.3–23.8‰; δ18OSO4 = –0.2 to 1.3‰), and microthermometric data for primary fluid inclusions in barite (Th = 116°– 233°C; 0.0–1.7 wt % NaCl), are consistent with metal deposition at temperatures of ~200 ± 40°C (for Au-Cu mineralization in V2 pit) and ~150 ± 30°C (Ag mineralization in A39 pit) from a low-salinity, sulfur- and metal-rich magmatic-hydrothermal liquid that mixed with vapor-heated meteoric water. The mineralizing fluids initially had a high-sulfidation state, producing enargite-dominated ore with associated silicification of the early-altered wall rock. With time, the fluids evolved to an intermediate-sulfidation state, depositing sphalerite- and tennantite-dominated ore mineral assemblages. Void-filling massive dickite (δ18O = –1.1 to 2.1‰; δD = –121 to –103‰) with pyrite was deposited from an increasingly diluted magmatic-hydrothermal liquid (≥70% meteoric component) exsolved from a progressively degassed magma. Gypsum (δ34S = 11.4–19.2‰; δ18OSO4 = 0.5–3.4‰) occurs in veins within postmineralization faults and fracture networks, likely derived from early anhydrite that was dissolved by circulating meteoric water during extensional deformation. This process may explain the apparent scarcity of hypogene anhydrite in lithocaps elsewhere. While the Mt. Carlton system is similar to those that form subaerial high-sulfidation epithermal deposits, it also shares several key characteristics with magmatic-hydrothermal systems that form base and precious metal mineralization in shallow-submarine volcanic arc and back-arc settings. The lacustrine paleosurface features documented at Mt. Carlton may be useful as exploration indicators for concealed epithermal mineralization in similar extensional terranes elsewhere.

Chapter 22: Gold Deposits of the Yanacocha District, Cajamarca, Peru

The Yanacocha district of northern Peru has produced &gt;37 million ounces (Moz) Au since production commenced in 1993. Recognized as one of the world’s most prolific high-sulfidation epithermal gold districts, its discovery was made over a four-year period (1984–1988) through a joint venture alliance operated by Newmont Corporation. Over the past 30 years the geologic understanding of the district has been enhanced by research and documentation by many academic and Newmont geoscientists. The gold deposits are hosted within Tertiary volcanic rocks consisting of pyroclastic sequences cut by several generations of breccias and intrusions, all of which have undergone silicic and advanced argillic alteration. A dominant NE-trending structural corridor bounds all deposits in the district, and local northwest fault intersections with this trend are complimentary controls on mineralization. There are 12 major deposits discovered and exploited at Yanacocha. The largest, Cerro Yanacocha, has produced &gt;17.5 Moz Au, whereas the newest deposit to be delineated, Antonio, has a &gt;1.0 Moz resource. The depletion of shallow, supergene-oxidized deposits has necessitated the current underground development to exploit deeper sulfide deposits. Significant potential remains within the Yanacocha district in both oxide and sulfide deposits, and ongoing exploration efforts, are leveraging learnings from mined deposits and advances in exploration technologies and tools to extend the mine life.

Comparison of Different Algorithms to Map Hydrothermal Alteration Zones Using ASTER Remote Sensing Data for Polymetallic Vein-Type Ore Exploration: Toroud–Chahshirin Magmatic Belt (TCMB), North Iran

Polymetallic vein-type ores are important sources of precious metal and a principal type of orebody for various base-metals. In this research, Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) remote sensing data were used for mapping hydrothermal alteration zones associated with epithermal polymetallic vein-type mineralization in the Toroud–Chahshirin Magmatic Belt (TCMB), North of Iran. The TCMB is the largest known goldfield and base metals province in the central-north of Iran. Propylitic, phyllic, argillic, and advanced argillic alteration and silicification zones are typically associated with Au-Cu, Ag, and/or Pb-Zn mineralization in the TCMB. Specialized image processing techniques, namely Selective Principal Component Analysis (SPCA), Band Ratio Matrix Transformation (BRMT), Spectral Angle Mapper (SAM) and Mixture Tuned Matched Filtering (MTMF) were implemented and compared to map hydrothermal alteration minerals at the pixel and sub-pixel levels. Subtle differences between altered and non-altered rocks and hydrothermal alteration mineral assemblages were detected and mapped in the study area. The SPCA and BRMT spectral transformation algorithms discriminated the propylitic, phyllic, argillic and advanced argillic alteration and silicification zones as well as lithological units. The SAM and MTMF spectral mapping algorithms detected spectrally dominated mineral groups such as muscovite/montmorillonite/illite, hematite/jarosite, and chlorite/epidote/calcite mineral assemblages, systematically. Comprehensive fieldwork and laboratory analysis, including X-ray diffraction (XRD), petrographic study, and spectroscopy were conducted in the study area for verifying the remote sensing outputs. Results indicate several high potential zones of epithermal polymetallic vein-type mineralization in the northeastern and southwestern parts of the study area, which can be considered for future systematic exploration programs. The approach used in this research has great implications for the exploration of epithermal polymetallic vein-type mineralization in other base metals provinces in Iran and semi-arid regions around the world.

Mineralogical Study of the Advanced Argillic Alteration Zone at the Konos Hill Mo–Cu–Re–Au Porphyry Prospect, NE Greece

The Konos Hill prospect in NE Greece represents a telescoped Mo–Cu–Re–Au porphyry occurrence overprinted by deep-level high-sulfidation mineralization. Porphyry-style mineralization is exposed in the deeper parts of the system and comprises quartz stockwork veins hosted in subvolcanic intrusions of granodioritic composition. Ore minerals include pyrite, molybdenite, chalcopyrite, and rheniite. In the upper part of the system, intense hydrothermal alteration resulted in the formation of a silicified zone and the development of various advanced argillic alteration assemblages, which are spatially related to N–S, NNW–SSE, and E–W trending faults. More distal and downwards, advanced argillic alteration gradually evolves into phyllic assemblages dominated by quartz and sericite. Zunyite, along with various amounts of quartz, alunite, aluminum phosphate–sulfate minerals (APS), diaspore, kaolinite, and minor pyrophyllite, are the main minerals in the advanced argillic alteration. Mineral-chemical analyses reveal significant variance in the SiO2, F, and Cl content of zunyite. Alunite supergroup minerals display a wide compositional range corresponding to members of the alunite, beudantite, and plumbogummite subgroups. Diaspore displays an almost stoichiometric composition. Mineralization in the lithocap consists of pyrite, enargite, tetrahedrite/tennantite, and colusite. Bulk ore analyses of mineralized samples show a relative enrichment in elements such as Se, Mo, and Bi, which supports a genetic link between the studied lithocap and the underlying Konos Hill porphyry-style mineralization. The occurrence of advanced argillic alteration assemblages along the N–S, NNW–SSE, and E–W trending faults suggests that highly acidic hydrothermal fluids were ascending into the lithocap environment. Zunyite, along with diaspore, pyrophyllite, and Sr- and Rare Earth Elements-bearing APS minerals, mark the proximity of the hypogene advanced argillic alteration zone to the porphyry environment.

Multistage alteration, mineralization and ore–forming fluid properties at the Viper (Sappes) Au–Cu–Ag–Te ore body, W. Thrace, Greece.

The mineralogy of ore and hydrothermal alteration of the high-sulfidation enargite–Au–Ag–Te Viper (Thrace) orebody, and fluid inclusions, were studied in drillcore samples. The hydrothermal system has evolved through several stages from pre-ore advanced argillic I+vuggy silica alteration, ore-stage advanced argillic II+vuggy silica alteration and silicification that has developed to argillic alteration (sericite)+silicification through pH increase, and a return to acid conditions as crosscutting post-ore advanced argillic alteration III+silicification. Ore is characterized by early barren pyrite I corroded by: (i) enargite–Au± complex Pb–Bi–Cu sulfosalts, tellurides and selenides, coexisting with euhedral quartz, and (ii) zoned pyrite II distinguished by anomalous concentrations of Au, Cu, As, Te, Bi, Pb, Se, within vuggy quartz. High-grade gold ore is also intergrown with late brecciacementing and vein-type epithermal-like banded quartz+ pyrite. These alteration and mineralization observations are consistent with the changing composition, water fugacity, and density of an expanding column of metal-laden magmatic vapor, combined with changes in structural permeability. Part of the enargite─Au─ quartz assemblages have been probably quenched from sulfosalt melt at high─temperatures (>575°C). End product of the enargite–sulfhide–silica crystallization sequence is the formation of high-grade epithermal quartz-gold colloformbanded ore during cooling and/or dilution/mixing down to ~200°C.