Propylitic Zone Research Articles

Petrography and Mineral Chemistry of Magmatic and Hydrothermal Biotite in Porphyry Copper-Gold Deposits: A Tool for Understanding Mineralizing Fluid Compositional Changes During Alteration Processes

DOI: 10.17014/ijog.5.1.47-64This study aims to understand the petrography and chemistry of both magmatic and hydrothermal biotites in porphyry copper-gold deposits, and to evaluate the fluid compositional changes during alteration processes. A total of 206 biotite grains from selected rock samples taken from the Batu Hijau porphyry Cu-Au deposit was analyzed. Detailed petrography and biotite chemistry analysis were performed on thin sections and polished thin sections, respectively, representing various rocks and alteration types. A JEOL JXA-8900R electron microprobe analyzer (EMPA) was used for the chemistry analysis. The biotite is texturally divided into magmatic and hydrothermal types. Ti, Fe, and F contents can be used to distinguish the two biotite types chemically. Some oxide and halogen contents of biotite from various rocks and alteration types demonstrate a systematic variation in chemical composition. Biotite halogen chemistry shows a systematic increase in log (XCl/XOH) and decrease in log (XF/XOH) values from biotite (potassic) through chlorite-sericite (intermediate argillic) to actinolite (inner propylitic) zones. The y-intercepts on the log (XCl/XOH) vs. XMg and log (XF/XOH) vs. XFe plotted for biotite from potassic and intermediate argillic zones are similar or slightly different. In contrast, the y-intercepts on the log (XCl/XOH) vs. XMg and log (XF/XOH) vs. XFe plotted for biotite from inner propylitic zone display different values in comparison to the two alteration zones. Halogen (F,Cl) fugacity ratios in biotite show a similar pattern: in the potassic and intermediate argillic zones they show little variation, whereas in the inner propylitic zone they are distinctly different. These features suggest the hydrothermal fluid composition remained fairly constant in the inner part of the deposit during the potassic and intermediate argillic alteration events, but changed significantly towards the outer part affected by inner propylitic alteration. High halogen content, particularly Cl, in hydrothermal biotite may portray that copper and gold were transported in mineralizing fluids in the form of chloride complexes CuCl2- and AuCl2-, respectively.

The Kago low-sulfidation gold and silver deposit: A peripheral mineralisation to the Nansatsu high-sulfidation system, southern Kyushu, Japan

The Kago deposit is a small deposit located at the southern tip of the Satsuma Peninsula of Southern Kyushu, Japan. It lies proximal to the well-known Nansatsu-type mineralisation province dominated by high-sulfidation type epithermal deposits. The deposit was heavily mined in the 18 th Century, largely for its relatively higher gold compared to that of surrounding and regional deposits. The Kago deposit is a typical low-sulfidation deposit, characterised by adularia-quartz veins, composed of electrum, Ag-tetrahedrite, polybasite, chalcopyrite and pyrite. Based on mine records, the grade ranged from 4.1 to 13.3 g/t Au and 2.6–6.6 g/t Ag. Alteration grades from low to high temperature argillic into a propylitic zone at the extremes of the vein exposures. Carbonate is absent. Fluid inclusion microthermometry reveals a typical temperature range of 220–240 °C with salinity of 0.7–2.6 NaCl eq. wt%. Electrum from high-grade ore ranges from 66 to 69 wt% Au. 40Ar/39Ar age dating of adularia bearing colloform/crustiform and brecciated veins, suggests a mineralisation event from 4.23 to 4.0 Ma. δ18O of veined and silicified quartz ranges from +4.0 to +18.4‰. δ18OH2O of fluids in equilibrium with quartz, in the dominant range of measured fluid inclusion temperatures, ranges from −6.5‰ to −0.2‰. δ34S of pyrite has a narrow range from −1.8 to 2.7‰. The deposit lies at the northern extent of the classic Nansatsu high-sulfidation epithermal area, in which a number of silicified bodies punctuate the region in a roughly semi-circular shape. The Kago deposit lies within the principle mineralisation age range of the high-sulfidation deposits, which range from 5.5 to 3.7 Ma. The structural displacement of the Kago deposit from the Nansatsu mineralisation and the differing host rocks has greatly influenced alteration, ore and rock-water interaction of the ore depositing fluids. Here we seek to establish the relationship that this extended mineral province has between the differing styles of mineralisation.

COMPARING INDEPENDENT COMPONENT ANALYSIS WITH PRINCIPLE COMPONENT ANALYSIS IN DETECTING ALTERATIONS OF PORPHYRY COPPER DEPOSIT (CASE STUDY: ARDESTAN AREA, CENTRAL IRAN)

Abstract. The image processing techniques in transform domain are employed as analysis tools for enhancing the detection of mineral deposits. The process of decomposing the image into important components increases the probability of mineral extraction. In this study, the performance of Principal Component Analysis (PCA) and Independent Component Analysis (ICA) has been evaluated for the visible and near-infrared (VNIR) and Shortwave infrared (SWIR) subsystems of ASTER data. Ardestan is located in part of Central Iranian Volcanic Belt that hosts many well-known porphyry copper deposits. This research investigated the propylitic and argillic alteration zones and outer mineralogy zone in part of Ardestan region. The two mentioned approaches were applied to discriminate alteration zones from igneous bedrock using the major absorption of indicator minerals from alteration and mineralogy zones in spectral rang of ASTER bands. Specialized PC components (PC2, PC3 and PC6) were used to identify pyrite and argillic and propylitic zones that distinguish from igneous bedrock in RGB color composite image. Due to the eigenvalues, the components 2, 3 and 6 account for 4.26% ,0.9% and 0.09% of the total variance of the data for Ardestan scene, respectively. For the purpose of discriminating the alteration and mineralogy zones of porphyry copper deposit from bedrocks, those mentioned percentages of data in ICA independent components of IC2, IC3 and IC6 are more accurately separated than noisy bands of PCA. The results of ICA method conform to location of lithological units of Ardestan region, as well.

Characteristics of a Low-Sulfidation Epithermal Deposit in the River Reef Zone and the Watuputih Hill, the Poboya Gold Prospect, Central Sulawesi, Indonesia: Host Rocks and Hydrothermal Alteration

Systematic exploration has delineated significant gold mineralization in the River Reef Zone and the presence of a siliceous body at Watuputih Hill, which is a Poboya gold prospect in Central Sulawesi, Indonesia. The mineralization is hosted within the Palu Metamorphic Complex. The host rocks consist of granite, biotite gneiss, and biotite schist, which is intercalated by feldspar porphyroblastic biotite schist and amphibolitic schist. The X-ray fluorescence (XRF) analysis of the granite and biotite gneiss suggests that the granitic rocks can be characterized as magnesian arc calc-alkaline rocks, with a weakly peraluminous composition. Alteration minerals were analyzed by a combination of petrographic and X-ray diffraction (XRD). In the River Reef Zone, the hydrothermal alteration zones can be sorted by their proximity to the primary fluid conduit and divided into inner, high-T, and low-T propylitic zones. In Watuputih Hill, the hydrothermal alteration can be divided into advanced argillic and argillic zones. The hydrothermal alteration assemblages indicated that the fluid was at a near-neutral pH in the River Reef Zone, whereas the fluid was acidic within Watuputih Hill. Because the hill is relatively distant from the River Reef Zone, the presence of these zones at Watuputih Hill may be indicative of another mineralization system beneath the hill.

Characteristics and 40Ar/39Ar Geochronology of the Erdenet Cu-Mo Deposit, Mongolia

The Early to Middle Triassic Erdenet porphyry Cu-Mo deposit, in northern Mongolia, developed in a continent-continent arc collision zone, within the Central Asian orogenic belt. The porphyry system is related to multiple intrusions of crystal-crowded biotite granodiorite porphyry, which formed a composite stock about 900 m in diameter, with multiple porphyritic microgranodiorite dikes. Wall rocks are Late Permian to Early Triassic, medium-grained granodiorite, with similar whole-rock geochemistry, mineralogy, and composition to the granodiorite porphyry. Whole-rock analysis of the granodiorite porphyry and wall rocks shows that these rocks cannot be discriminated, but both have depleted middle heavy rare earth elements and Y, typical of fertile porphyry magmatic suites. At the current pit level (1,250 m elev), early porphyry-style quartz veins (A and B type) are locally infilled by pyrite-chalcopyrite, with subordinate bornite, but most of the chalcopyrite occurs in D veins that constitute more than 50% of the Cu grade (~0.5 wt % Cu). The 0.3 wt % Cu shell resembles a molar tooth, enveloping the granodiorite porphyry, with deeper roots extending down the wal-rock contacts. Molybdenite occurs in monomineralic veins, and in finely laminated to massive quartz-molybdenite veins. The most important alteration is quartz-muscovite, which occurs as relatively coarse (100–500 μ m) alteration selvages (1–5 cm) that envelop D veins. The D veins cut illite ± kaolinite-smectite (or intermediate argillic) alteration. Intermediate argillic alteration, together with abundant pink anhydrite (commonly hydrated to gypsum), extends from at least 1,300- to 900-m elevation in the deepest drill holes, and has overprinted early potassic alteration, or relatively unaltered red granodiorite. Meter-wide zones of kaolinite cut the anhydrite-gypsum at all levels. There is an abrupt transition outward from the intermediate argillic alteration to chlorite-epidote (propylitic) alteration, at 50 to 200 m from the granodiorite porphyry contact, although D veins (and chalcopyrite) extend outward to the propylitic zone. The Erdenet porphyry system, was overprinted by advanced argillic alteration, which outcrops 2 km northwest of the pit, and forms a lithocap that extends over 10 × 2.5 km. It is characterized by residual quartz, andalusite, Na-Ca and K-alunite, diaspore, pyrophyllite, zunyite, topaz, dickite, and kaolinite. The upper part of the porphyry Cu-Mo deposit (removed by mining), comprised a bornite-chalcocite enriched zone up to 300 m thick with an average grade of 0.7 wt % Cu and up to 5 wt % Cu locally. Based on hypogene bornite-chalcocite mineral textures and high-sulfidation state mineralogy, the enriched zone is inferred to be of hypogene origin, but modified by supergene processes. Consequently, it may be related to formation of the lithocap. Previous Re-Os dates of 240.4 and 240.7 ± 0.8 Ma for molybdenite in quartz veins are comparable to new 40 Ar/ 39 Ar dates of 239.7 ± 1.6 and 240 ± 2 Ma for muscovite that envelops D veins. One 40 Ar/ 39 Ar date on K-alunite from the lithocap of 223.5 ± 1.9 Ma suggests that it may be about 16 m.y. younger than Erdenet, but this result needs to be verified by further dating.

Discrimination between mineralized and unmineralized alteration zones using primary geochemical haloes in the Darreh-Zar porphyry copper deposit in Kerman, southeastern Iran

Primary geochemical haloes were studied at the Darreh-Zar porphyry Cu-deposit, southern Iran. In terms of geochemical signatures, high K2O/Na2O enrichment, HREEs and HFSE's depletion in the potassic alteration, high (La/Sm)cn, (La/Yb)cn and (Gd/Yb)cn ratios in mineralized sericitic and potassic zones and notable depletion in the REEs content in argillic alteration is recognized. Further, Mg, Li, Sc, P enrichment and W depletion can serve to separate potassic alteration from the other altered zones, while (Eu/Eu*)cn and (Ce/Ce*)cn don't show pronounced changes in different alteration zones. The coupled positive Tl, Se, S, Rb, Co, Cs, Mo, K and negative Te, Ta, Ti, Sr, Rb, As, Bi, Ga, Hf, In, Mn, Zn and Zr anomalies can be adequately used in discriminating between the mineralized zones (potassic, chlorite-sericite and sericite alterations) and the barren (propylitic zone). The behavior of the trace elements on isocon diagrams reveal that HFSEs are depleted in mineralized altered zones and display variations in the amounts in the barren facies.Zonality index in the axial direction from drill holes 146 to 124 estimates the zonality sequence as Pb-Zn-Ag-Cu-Pb-Zn in the surface horizons. The calculated zonality in five drill holes and six levels indicates that the level of 550 m at the DH 117 in the central part of the area has the highest value (0.76) for Cu. The zonality sequence from the surface to the depth is variable and can be demonstrated as follow: DH 146: Pb-Zn-Cu-Mo-Ag; DH 137: Zn-Cu-Mo-Pb-Ag; DH 117: Ag-Zn-Pb-Mo-Cu; DH: 121: Cu-Mo-Zn-Ag-Pb; DH 136: Pb-Ag-Zn-Cu-Mo; DH 124: Zn-Mo-Cu-Pb-Ag. Available data of the enrichment factors shows different enrichment for copper and molybdenum (i.e. EF > 10), selenium and silver (i.e. EF > 5), tin and LREEs (i.e. 1 < EF < 5).

Copper–arsenic decoupling in an active geothermal system: A link between pyrite and fluid composition

Over the past few decades several studies have reported that pyrite hosts appreciable amounts of trace elements which commonly occur forming complex zoning patterns within a single mineral grain. These chemical zonations in pyrite have been recognized in a variety of hydrothermal ore deposit types (e.g., porphyry Cu–Mo–Au, epithermal Au deposits, iron oxide–copper–gold, Carlin-type and Archean lode Au deposits, among others), showing, in some cases, marked oscillatory alternation of metals and metalloids in pyrite growth zones (e.g., of Cu-rich, As–(Au, Ag)-depleted zones and As–(Au, Ag)-rich, Cu-depleted zones). This decoupled geochemical behavior of Cu and As has been interpreted as a result of chemical changes in ore-forming fluids, although direct evidence connecting fluctuations in hydrothermal fluid composition with metal partitioning into pyrite growth zones is still lacking. In this study, we report a comprehensive trace element database of pyrite from the Tolhuaca Geothermal System (TGS) in southern Chile, a young and active hydrothermal system where fewer pyrite growth rims and mineralization events are present and the reservoir fluid (i.e. ore-forming fluid) is accessible. We combined the high-spatial resolution and X-ray mapping capabilities of electron microprobe analysis (EMPA) with low detection limits and depth-profiling capacity of secondary-ion mass spectrometry (SIMS) in a suite of pyrite samples retrieved from a ∼1km drill hole that crosses the argillic (20–450m) and propylitic (650–1000m) alteration zones of the geothermal system. We show that the concentrations of precious metals (e.g., Au, Ag), metalloids (e.g., As, Sb, Se, Te), and base and heavy metals (e.g., Cu, Co, Ni, Pb) in pyrite at the TGS are significant. Among the elements analyzed, As and Cu are the most abundant with concentrations that vary from sub-ppm levels to a few wt.% (i.e., up to ∼5wt.% As, ∼1.5wt.% Cu). Detailed wavelength-dispersive spectrometry (WDS) X-ray maps and SIMS depth vs. isotope concentration profiles reveal that pyrites from the TGS are characterized by chemical zoning where the studied elements occur in different mineralogical forms. Arsenic and Co occur as structurally bound elements in pyrite, Cu and Au in pyrite can occur as both solid solution and submicron-sized particles of chalcopyrite and native Au (or Au tellurides), respectively. Pyrites from the deeper propylitic zone do not show significant zonation and high Cu–(Co)–As concentrations correlate with each other. In contrast, well-developed zonations were detected in pyrite from the shallow argillic alteration zone, where Cu(Co)-rich, As-depleted cores alternate with Cu(Co)-depleted, As-rich rims. These microanalytical data were contrasted with chemical data of fluid inclusions in quartz and calcite veins (high Cu/As ratios) and borehole fluid (low Cu/As ratios) reported at the TGS, showing a clear correspondence between Cu and As concentrations in pyrite-forming fluids and chemical zonation in pyrite. These observations provide direct evidence supporting the selective partitioning of metals into pyrite as a result of changes in ore-forming fluid composition, most likely due to separation of a single-phase fluid into a low-density vapor and a denser brine, capable of fractionating Cu and As.

PROMINE

The research sites are located in the village of Berambang, Sekotong District, West Lombok Regency,West Nusa Tenggara Province. This area was dominated by volcanic rocks composed of dasiticvolcanic rock, diatrema breccia, and diorite intrusion. Berambang area shows alteration in the form ofpotassic, propylitic, advanced argillic, and argillic alterations where in some places accompanied bypyritisation and stockwork structure, the type of mineralization in this area is a porphyry copper-goldtype. In the potasic alteration zone there are minerals that have a strong anomaly response to themagnetic due to the presence of oxide minerals magnetite (Fe2O3). Mineral sulfides such as pyrite(FeS2) and chalcopyrite (CuFeS2) will also provide significant anomalous responses that have anabundance of 2-5% in the potassic zone. In a propylitic alteration zone characterized by chlorite,calcite and epidote minerals that do not respond to magnetic anomalies, the presence of pyriteminerals, hematites and chalcopyrite with abundance of ≤1% will provide some magnetic anomaly inthe propylitic zone. As for advanceargillic alteration zones characterized by mineral andalusite, aluniteand quartz, there will not be any magnetic anomalies, the phenomena was due to the rarity ofmineralization in this zone gives an insignificant anomalous impact. Meanwhile, for the argillic zonecharacterized by mineral illite, kaolinite and smectite will not have anomalous magnetic impact, veryrare mineralization in the argillic zone so that the magnetic anomaly is not significant. From the floatingEuler 3D shows an anomalous source from a depth of 0 meters to a depth of more than 400 meters.

Integrating Data of ASTER and Landsat-8 OLI (AO) for Hydrothermal Alteration Mineral Mapping in Duolong Porphyry Cu-Au Deposit, Tibetan Plateau, China

One of the most important characteristics of porphyry copper deposits (PCDs) is the type and distribution pattern of alteration zones which can be used for screening and recognizing these deposits. Hydrothermal alteration minerals with diagnostic spectral absorption properties in the visible and near-infrared (VNIR) through the shortwave infrared (SWIR) regions can be identified by multispectral and hyperspectral remote sensing data. Six Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) bands in SWIR have been shown to be effective in the mapping of Al-OH, Fe-OH, Mg-OH group minerals. The five VNIR bands of Landsat-8 (L8) Operational Land Imager (OLI) are useful for discriminating ferric iron alteration minerals. In the absence of complete hyperspectral coverage area, an opportunity, however, exists to integrate ASTER and L8-OLI (AO) to compensate each other’s shortcomings in covering area for mineral mapping. This study examines the potential of AO data in mineral mapping in an arid area of the Duolong porphyry Cu-Au deposit(Tibetan Plateau in China) by using spectral analysis techniques. Results show the following conclusions: (1) Combination of ASTER and L8-OLI data (AO) has more mineral information content than either alone; (2) The Duolong PCD alteration zones of phyllic, argillic and propylitic zones are mapped using ASTER SWIR bands and the iron-bearing mineral information is best mapped using AO VNIR bands; (3) The multispectral integration data of AO can provide a compensatory data of ASTER VNIR bands for iron-bearing mineral mapping in the arid and semi-arid areas.

Geological setting for porphyry copper deposits in calc-alkaline rocks: Wadi Rofaiyed area, Sinai, Egypt

The close association of copper mineralization with porphyritic quartz diorite and intermediate volcanic rocks, the presence of hydrothermal alteration zones, the disseminated nature of sulfide minerals, and extremely absence of massive lenses and the volcanic arc (orogenic) tectonic situation of ore-bearing rocks are the main geological conditions associated with diorite-type porphyry copper system at Wadi Rofaiyed area, Sinai, Egypt. Chalcopyrite and pyrite are the main sulfide minerals in quartz diorite, whereas chalcopyrite, pyrite, galena, and sphalerite are the main sulfide minerals in Rutig volcanics. Secondary sulfide minerals include chalcocite and covellite. Quartz diorite and Rutig volcanics (intermediate composition) are calc-alkaline, enriched in large ion lithophile elements (LILEs) and depleted in high field strength elements (HFSEs). The incompatible trace element patterns favor fractional crystallization of plagioclase and Fe-Ti oxides. Rutig volcanics developed in orogenic arc-type and anorogenic within plate, indicating an eruption in a transitional post-collisional tectonic setting. Two hydrothermal events are thought to take place, which are characterized by zonal pattern composed of a central potassic zone and a peripheral propylitic zone. Both zones are centered over porphyritic intrusive rocks that might be considered the source of hydrothermal solutions. A close relationship of mineralization to pre-Katerina ring dike structures, namely, joints and faults, was revealed. Generally, the gentle dips of bandings in Rutig volcanics and the presence of post-eruption faulting indicate a significant deformation by translational and rotational movement. The average thickness of Rutig volcanics is about 1.4 km, which along with the big masses of intrusive country rocks constitute a considerable volume of mineralized stock. Meanwhile, subsidence of Rutig volcanics which served as capping rocks played, to some extent, an effective role in preserving the mineralization in the underlying country rocks. Multi-scale structural investigations revealed the role of interstitial spaces and fracture network in localizing mineralization. Where two styles of mineralization are recognized, the first is dissemination and the second is fracture filling. The mineralization was formed during a large-scale extensional tectonic event that followed the collisional period.

The Chahnaly Low-Sulfidation Epithermal Gold Deposit, Western Makran Volcanic Arc, Southeast Iran

The Chahnaly low-sulfidation epithermal Au deposit and nearby Au prospects are located northwest of the intermittently active Bazman stratovolcano on the western end of the Makran volcanic arc, which formed as the result of subduction of the remnant Neo-Tethyan oceanic crust beneath the Lut block. The arc hosts the Siah Jangal epithermal and Kharestan porphyry prospects, near Taftan volcano, as well as the Saindak Cu-Au porphyry deposit and world-class Reko Diq Cu-Au porphyry deposit, near Koh-i-Sultan volcano to the east-northeast in Pakistan. The host rocks for the Chahnaly deposit include early Miocene andesite and andesitic volcaniclastic rocks that are intruded by younger dacitic domes. Unaltered late Miocene dacitic ignimbrites overlie these rocks. Laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) U-Pb zircon geochronology data yield ages between 21.8 and 9.9 Ma for the acidic-intermediate regional volcanism. The most recent volcanic activity of the Bazman stratovolcano involved extrusion of an olivine basalt during Pliocene to Quaternary times. Interpretation of geochemical data indicate that the volcanic rocks are synsubduction and calc-alkaline to subalkaline. The lack of a significant negative Eu anomaly, a listric-shaped rare earth element pattern, and moderate La/Yb ratios of host suites indicate a high water content of the source magma. Gold and electrum are temporally and spatially related to a series of structurally controlled, 030°-trending, subvertical hydrothermal breccias with chalcedony-adularia that cut porphyritic andesite and andesitic volcaniclastic rocks. Gold is associated with pyrite, a siliceous matrix of hydrothermal breccia, and previously formed vein clasts, as well as with iron oxides and hydroxides in oxidized zones. Rare silver minerals include Ag-bearing electrum and naumannite, iodargyrite, an unnamed silver diiodide, and hessite. Hydrothermal alteration is generally well developed surrounding the ore-bearing hydrothermal breccia. The main types of alteration in the area include an inner ~0.5- to 20-m-thick gold-bearing hydrothermal breccia composed of quartz-chalcedonyadularia-illite-pyrite, a ~5- to 50-m-thick zone of quartz, chalcedony, pyrite, illitic phengite, phengite, illitic muscovite, illite, illitic paragonite, paragonite, muscovite, montmorillonite and, rarely, siderite, and a 30- to 70-m outer propylitic zone of Fe-Mg chlorite, calcite, ankerite, dolomite, epidote, palygorskite, and pyrite. The Chahnaly Au deposit formed during the early stages of magmatism. LA-ICP-MS zircon U-Pb geochronology of host andesite and 40Ar/39Ar dating of two samples of gold-associated adularia show that the ore-stage adularia (19.83 ± 0.10 and 19.2 ± 0.5 Ma) is younger, by as much as 1.5 million years, than the volcanic host rock (20.32 ± 0.4 Ma). Therefore, either hydrothermal activity continued well after volcanism or a second magmatic event rejuvenated hydrothermal activity. This second magmatic event may be related to eruption of porphyritic andesite at ~20.32 ± 0.40 Ma, which is within error of ~19.83 ± 0.10 Ma adularia. The new LA-ICP-MS zircon U-Pb host rock and vein adularia 40Ar/39Ar ages suggest that early Miocene magmatism and mineralization in the Bazman area is of a similar age to that of the Saindak porphyry and Tanjeel porphyry center of the giant Reko Diq deposit. This confirms the existence of early Miocene arc magmatism and mineralization along the Iranian part of the Makran volcanic arc. Ore, alteration mineralogy, and alteration patterns indicate that the Chahnaly deposit is a typical low-sulfidation epithermal Au deposit, located in a poorly explored part of the Makran volcanic arc in Iran.

Characteristics of the Copper Mineralization in Tsogttsetsii Area, Mongolia

반암동 광화작용이 수반된 관입암체로 이루어진 촉트체치 지역은 몽골 남부 중앙아시아 조산대의 구르반사이한 호상열도 지형에 위치한다. 이러한 촉트체치 지역에서 예비조사를 수행하였다. 촉트체치 지역의 동 광화작용은 페름기에 관입한 알칼리 화강암과 관련된 반암동 광상이다. 공작석이 산출되는 알칼리 화강암 지역에서 프로필리틱 변질대가 넓게 분포한다. 편광현미경에서 확인된 광석광물은 자철석, 황철석, 반동석이다. 프로필리틱 변질대 시료에서는 석영, 견운모, 녹니석, 녹렴석 등이 관찰되었다. XRD와 SEM-EDS 분석 결과 동 광물은 주로 공작석과 적동석으로 이루어진다. 공작석 산출지에서 채취한 시료의 평균 동 함량은 759 ppm이고 최대 동 함량은 6190 ppm이다. 촉트체치 지역의 광화작용 특성은 촉트체치 지역으로부터 남쪽으로 56 km 떨어진 오유 톨고이 동-금(-몰리브덴) 광상 및 북동쪽으로 120 km 떨어진 차간 수바르가 동-몰리브덴 광상과 유사하다. 조사지역의 지질, 지구조 환경, 암상, 광물, 변질 등이 다른 반암동 광상과 유사한 특성을 갖는다. 따라서 촉트체치동 광화 지역에 대해 지하 광체 확인을 위한 IP 탐사를 포함한 추가 광물자원 탐사가 필요하다.

Mineralization and trace element distribution in pyrite using EMPA in exploration drill holes from Cheshmeh Zard gold district, Khorasan Razavi Province, Iran

ناحیه مطالعاتی در شمال استان خراسان رضوی و 45 کیلومتری جنوب نیشابور قرار دارد. رگه های طلادار درون سنگهای گرانیت، گرانودیوریت، گرانودیوریت پورفیری، آندزیت، برش و توف نفوذ کرده اند. رگه ها از جنس کوارتز و کلسیت هستند. مناطق اصلی دگرسانی شامل منطقه سرسیتیک، سیلیسی، پروپلیتیک و منطقه کربنات است. کانی زایی به‌طور نزدیکی با دگرسانیهای سیلیسی و سرسیتیک به شکل رگه‌چه و با منطقه پروپلیتیک به شکل افشان همراه است. کانی شناسی کانیهای باطله کوارتز، کلسدونی، سرسیت، آدولاریا، کلسیت، دولومیت، ایلیت، دیکیت، آلبیت، کائولینیت و کلریت است. کانی زایی رگه ای عمدتا با رگه‌چه ها، برش، افشان و استوک ورک همراه هستند. رگه‌چه ها از پیریت، مارکازیت، آرسنوپیریت و کمتر کالکوپیریت، اسفالریت، گالن، مگنتیت و هماتیت تشکیل شده اند. بیشترین عیار طلا در رگه های سیلیسی دیده می شود. پیریت کانی سولفیدی اصلی در کانی سازی اولیه است. سه نوع پیریت بر اساس ترکیب شیمیایی شناسایی شده است: پیریت خالص، پیریت غنی از آرسنیک و پیریت تیتانیوم- وانادیوم دار. تجزیه های ریزکاوشگر الکترونی بیشترین غلظت آرسنیک، تیتانیوم و وانادیوم را به ترتیب 62/3، 91/3 و 53/0 درصد وزنی در پیریتهای رگه های طلادار نشان می دهند. طلا معمولا همراه با پیریت آرسنیک دار و پیریت تیتانیوم- وانادیوم دار است. براساس مطالعه بافت و ترکیب پیریتها، رگه‌چه‌های پیریت آرسنیک دار همراه با کانیهای سولفیدی آرسنوپیریت، کالکوپیریت، گالن، اسفالریت در دمای بالا و با کاهش دما و فشار، پیریتهای فرامبوئیدال با حاشیه حاوی آرسنیک و طلا شکل گرفته اند و در ادامه پیریتهای درشت تیتان دار به‌وجود آمده اند. پیریتهای خالص و تأخیری درشت بلور آخرین فاز کانی ساز در منطقه هستند.

Hydrothermal Alteration of Miryang Pyrophyllite Deposit

Hydrothermal alteration patterns and environment are studied by mineral assemblages and chemical analyses of surface and core samples from Miryang pyrophyllite deposit. The alteration zones of this deposit can be divided into three zones on the basis of mineral assemblage; advanced argillic, phyllic, and propylitic zone. Advanced argillic zone mainly consists of pyrophyllite-dickite (-quartz) and corresponds to principal mining ore. The common mineral assemblage of phyllic zone and propylitic zone are sericite-quartz-dickite and chlorite-quartz, respectively. Horizontal and vertical alteration patterns and major element geochemistry indicate that pyrophyllite ores have been formed several times by hydrothermal alteration. And it also suggests that the huge ore bodies may be extended from the deeper part of recent quarries to the south-southeastern direction. The paragenesis of ore minerals and polytype (2M) suggest that ore deposit was formed at about 300-350℃.

Thermal history of the Acoculco geothermal system, eastern Mexico: Insights from numerical modeling and radiocarbon dating

Acoculco is a geothermal prospective area hosted by a volcanic caldera complex in the eastern Trans-Mexican Volcanic Belt. Surface manifestations are scarce and consist of gas discharges (CO2-rich) and acid-sulfate springs of low temperature, whereas hydrothermal explosive activity is profusely manifested by meter-scale craters and mounds of hydrothermal debris and breccias. Silicic alteration extends for several square kilometers around the zone with gas manifestations and explosive features, affecting surficial volcanic rocks, primarily tuffs and breccias. In the subsurface, an argillic alteration zone (ammonium illite) extends down to a depth of ∼600m, and underneath it a propylitic zone (epidote–calcite–chlorite) occurs down to ∼1000m.Thermal logs from an exploratory borehole (EAC-1, drilled in 1995 down to 1810m) showed a conductive heat transfer regime under high geothermal gradient (∼140°C/1000m). In contrast, the thermal profile established from temperatures of homogenization of fluid inclusions—measured on core samples from the same drill hole—suggests that convection occurred in the past through the upper ~1400m of the geothermal system. A drop in permeability due to the precipitation of alteration minerals would have triggered the cessation of the convective heat transfer regime to give place to a conductive one. With the purpose of determining when the transition of heat transfer regime occurred, we developed a 1D model that simulates the time-depth distribution of temperature. According to our numerical simulations, this transition happened ca. 7000years ago; this date is very recent compared to the lifespan of the geothermal system. In addition, radiocarbon chronology indicates that the hydrothermal explosive activity postdates the end of the convective heat transfer regime, having dated at least three explosive events, at 4867–5295, 1049–1417 and 543–709y cal. BP. Therefore, hydrothermal explosions arise from the self-sealing of the Acoculco geothermal system, involving a natural hazard that could affect future geothermal-power infrastructure.

Spatial pattern and dynamic control for mineralization in the Pulang porphyry copper deposit, Yunnan, SW China: Perspective from fractal analysis

The Pulang ore deposit, one of the largest porphyry copper deposits in China, is located in the Yidun continental arc, SW China. The alteration zones in the deposit transit upward and outward from early potassium-silicate, through quartz–sericite, to later propylitization. The wallrock near the porphyry stock was mostly changed into hornfels. The former two alterations host the main orebodies, constituting the core of mineralized zone; the later two alterations only develop weak mineralization surrounding the core. In this paper, various fractal indices, including the exponent of lacunarity, multifractal spectrum, correlation dimension and Hurst exponent, are applied to characterize the Cu spatial distribution in 114 drillcores in the Pulang ore deposit, with the aim to correlate the element spatial pattern with its dynamic drive. Compared to fractal indices in the propylitic zone and hornfels, the exponents of lacunarity in the potassium-silicate and quartz–sericite zones exhibit lower and more stable values, the correlation dimensions are higher and more consistent; yet the values of height difference of multifractal spectrum are lower and largely varied, and the Hurst exponents show little difference. Variations of the former three indices suggest that the core of mineralized zone has more homogeneity, stronger compactness of high concentrations, and greater proportion of high concentrations in the Cu distribution compared to the other parts of the deposit. More importantly, the correlation dimension, indicating the complexity of controls underpinning the system, is closely correlated to the exponent of lacunarity, which represents the homogeneity of spatial pattern. This correlation between those two indices implies a genetic link, that is to say the greater complexity of controls results in a more homogeneous spatial distribution of Cu in the porphyry deposit. The stability of the two indices is considered to reflect the development of thick orebody, providing a new perspective to understand the genesis of porphyry ore deposit. This interpretation from the fractal perspective is consistent with the geological understanding for the formation of porphyry deposits, which is considered to be subject to the complexity of ore fluid evolution with multifaceted physicochemical conditions. For a pragmatic use, these two fractal indices are successfully applied in the delineation of the core of mineralized zone in the plane view.

Evaluation of Earth Observing-1 (EO1) Data for Lithological and Hydrothermal Alteration Mapping: A Case Study from Urumieh-Dokhtar Volcanic Belt, SE Iran

This study evaluates the capability of Advanced Land Imager (ALI) and Hyperion Earth Observing-1 (EO1) data for lithological and hydrothermal alteration mapping. Several image processing methods were applied to ALI and Hyperion images covering the Meiduk and Sar Cheshmeh porphyry copper mining districts, SE Iran. Feature-oriented principal components selection, developed band ratio and minimum noise fraction methods were able to yield spectral information for enhancing the hydrothermally altered rocks and lithological units at regional scale using ALI data. Mixture-tuned matched-filtering method discriminated hydrothermal alteration areas from surrounding rock units using shortwave infrared bands of ALI. Analytical imaging and geophysics (AIG)-developed hyperspectral analysis processing methods were applied to the visible and near infrared and shortwave infrared bands of Hyperion for mapping iron oxide/hydroxide minerals and clay mineral assemblages at district scale. Supergene altered areas consisting of iron oxide/hydroxide minerals such as hematite, limonite, jarosite and goethite were detected using visible and near infrared bands of Hyperion. Phyllic, advanced argillic and propylitic alteration zones associated with porphyry copper mineralization were discriminated using shortwave infrared bands of Hyperion. The achievements of this investigation indicate considerable implications for geologists to use Earth Observing-1 data for porphyry copper and epithermal gold exploration.

The chlorite proximitor: A new tool for detecting porphyry ore deposits

The major, minor and trace element chemistry of chlorite were evaluated as a tool for mineral exploration in the propylitic environment of porphyry ore deposits. Chlorite from eighty propylitically altered samples, located up to 5km from the Batu Hijau Cu–Au porphyry deposit in Indonesia, was analyzed using electron microprobe and laser ablation inductively-coupled plasma mass spectrometry. The results show that a variety of elements, including K, Li, Mg, Ca, Sr, Ba, Ti, V, Mn, Co, Ni, Zn and Pb, are probably incorporated in the chlorite lattice and display systematic spatial variations relative to the porphyry center. Ti, V and Mg decrease exponentially in concentration with increasing distance, whereas the others increase. Ratioing the former to the latter provides a variety of ratios that vary up to four orders of magnitude, providing sensitive vectoring parameters. Chlorite geothermometry suggests that Ti is substituted into chlorite as a function of crystallization temperature and thus maps out the thermal anomaly associated with the mineralized center. By contrast, Mn and Zn display a maximum in chlorite at a distance of ~1.3km that mirrors the whole rock anomaly for these metals, reflecting their lateral advection into the wall rocks by magmatic-hydrothermal fluids. The recognizable footprint defined by chlorite compositions extends to at least 4.5km, significantly beyond the whole rock anomalism (≤1.5km) and thus represents a powerful new exploration tool for detecting porphyry systems. Variations in chlorite chemistry are very systematic in the inner propylitic zone (to distances of ~2.5km), thereby providing a precise vectoring tool in a domain where other tools are typically ineffective. In this zone, equations of the form:x=lnRabcan be formulated, where the distance to center, x, is predicted based on a variety of element ratios in chlorite R, and where a and b are exponential fit parameters. Importantly, distal chlorite compositions in porphyry-related propylitic alteration systems are also shown to be distinct from metamorphic chlorite, allowing the external fringes of porphyry-related hydrothermal systems to be distinguished from “background” regional metamorphism or geothermal alteration.

Lineament Tectonics and Mineralizatin in Tarom Area, North Iran

The study area that is part of Tarom volcano-plutonic zone which host many hydrothermal base metal deposits located in Zanjan, NW Iran. Understanding the tectonic events that can cause mineralization and hydrothermal alteration are significant factor in assessing the exploration potential of different structures. In this research, hydrothermal alteration such as Iron oxide, argillic, phyllic, and propylitic zones were determined by Spectral Angle Method (SAM) and also lineaments identified by high pass filters and hill-shade DEM techniques on Advanced Space borne Thermal Emission and Reflection Radiometer (ASTER) data. Field studies revealed most alteration and mineralization occurred in NE-SW fractures and control mineralization.

La Josefina Au–Ag deposit (Patagonia, Argentina): A Jurassic epithermal deposit formed in a hot spring environment

The La Josefina Jurassic epithermal Au–Ag deposit located in Patagonia, Argentina, developed in an extensional setting of a back-arc environment, associated with a widespread Middle–Late Jurassic calc-alkaline volcanism. Block faulting has juxtaposed shallow level features evidenced by hot spring manifestations, hydrothermal eruption breccias and Au-rich veins, which suggest that mineralization in these veins, could extend far below the depths already tested by core drilling. Veins are filled by quartz, chalcedony, opal and minor adularia and barite with massive, comb, cockade, colloform–crustiform bandings and lattice-bladed textures. Ore minerals include electrum, Ag-rich sulfosalts (freibergite), pyrite, galena, sphalerite, chalcopyrite and specular hematite with minor arsenopyrite, marcasite, tetrahedrite and bornite. Four mineralizing stages have been identified, the first two (S1 and S2) are Au and Ag-rich, with temperatures ranging from 225 to 290° and salinities from up to 15wt.% in S1 decreasing to ~1wt.% NaCl in S2. The third stage (S3) displays higher base metal contents at lower temperatures (~200°C). Finally, the last stage (S4) is barren with temperatures lower than 100°C. Veins are surrounded by a proximal alteration halo of quartz+pyrite±adularia±illite followed outwards by illite/smectite interstratified clays and smectites (with less chlorite) to a propylitic zone. Stable isotope values calculated for the fluids show a mostly meteoric origin for mineralization fluids. Such distinct features place the La Josefina deposits in a hot spring environment with evidences of being formed at a proximal position of the Jurassic paleosurface and paleowater level.