Hydrothermal Alteration and Cu-Au Mineralization at Nena High Sulfidation-type Deposit, Frieda River, Papua New Guinea

Abstract. The Nena Cu‐Au deposit, located in the Frieda River mineral district of northwestern mainland Papua New Guinea, is a composite structurally‐lithologically controlled high sulfidation (HS) system. Its hydrothermal alteration and Cu‐Au mineralization are presented in this paper. Initially propylitized andesitic volcanics veined by epithermal quartz were pervasively superimposed by zoned HS alteration. The zonation grades from vuggy silica core to sulfur‐rich, pyritic silica‐alunite halo followed by pyrophyllite‐dickite‐kaolinite interval and finally to thin illite‐smectite margin, suggesting progressive decrease in temperature and increase in pH. This zonation is enveloped by chlorite‐epidote‐calcite‐gypsum alteration. The acid altered rocks were then invaded by multiple phases of pyrite, subsequently crosscut by quartz, vein alunite and barite. Then sequential deposition of bladed covellite, enargite, luzonite and stibioluzonite occurred from the NW to the SE portions of the deposit, forming a zonation suggestive of progressive decrease in temperature, sulfur fugacity and sulfidation stage. Most ore mineralization occurs in the vuggy silica core. Gold mineralization commenced from the transition of enargite to luzonite and continued throughout the stibioluzonite stage. Associated with gold deposition are Au‐rich pyrite, tennantite‐tetrahedrite, chalcopyrite‐bornite, native tellurium, electrum, calaverite, bismuthinite and galena. Native sulfur occupied the remaining cavities and represents the waning stage of the hydrothermal system. Fluid inclusions studies distinguished magmatic (>300–350d?C, 9–15 wt% NaCl equiv.) and meteoric (<150–200d?C, 1–2 wt% NaCl equiv.) fluids (Holzberger et al., 1996). Temperatures and salinities of fluid inclusions from barite associated with Cu sulfides show a general decrease from NW (330d?C, 9–15 wt% NaCl equiv.) to SE (172d?C, 10 wt% NaCl equiv.) parts of the deposit, indicating gradual entrainment of ground water (Hitchman and Espi, 1997). Interaction of magmatic fluids with meteoric water accompanied by changes in temperature, salinity, acidity and oxidation state of the resultant fluids is interpreted to have been the main cause of metal precipitation. Finally, supergene processes generated Au zone with an underlying chalcocite‐covellite‐digenite blanket over the primary sulfides at depth. Gold occurs as lattice constituent in scorodite, limonite‐goethite and jarosite. Chalcocite is more abundant and widespread than other Cu sulfides. Acidic fluids deposited powdery alunite and kaolinite, vein alunite and amorphous silica. Weakly secondary biotite‐quartz altered porphyry located below the known HS Cu‐Au deposit contains chalcopyrite‐bornite and is overprinted by quartz‐alunite‐pyro‐phyllite‐pyrite assemblage. This feature indicates close temporal, spatial and genetic relation between the two deposit types.     

巴布亚新几内亚奥克泰迪铜金矿床成矿特征和控制因素

巴布亚新几内亚西部Fubilan山奥克泰迪矿床是一个世界级铜金矿床,在大地构造上位于新几内亚造山带的巴布亚褶皱带。该矿床的铜金矿化赋存于Fubilan二长斑岩及其周边的磁铁矿夕卡岩和硫化物夕卡岩中。矿石类型以原生硫化物矿石为主,金属矿物包括磁铁矿、黄铁矿、磁黄铁矿、白铁矿、黄铜矿、斑铜矿等。蚀变类型包括夕卡岩化、钾化、泥化和青盘岩化。矿床氧化次生富集带发育,表生矿石矿物为蓝辉铜矿、辉铜矿、自然铜、铜蓝和银金矿。成矿作用主要受区域构造、侵入杂岩体、Darai组灰岩地层、断裂等因素的控制。根据矿床的主岩、矿石特征、蚀变特征和控矿因素,认为该矿床成因类型属于较为典型的夕卡岩一斑岩型矿床。     

北祁连天鹿铜矿床砂岩型铜矿石特征

天鹿铜矿床是古生代海相砂页岩型铜矿.其铜矿石主要为粉砂岩型,包括斑铜矿矿石、辉铜矿矿石、辉铜矿斑铜矿矿石、黄铜矿斑铜矿矿石、黄铜矿矿石、黄铁矿黄铜矿矿石等6种自然类型.矿石结构主要为结晶结构和交代结构,矿石构造以浸染状为主.主矿层中的矿化沿岩层垂向具有明显的分带性,从底部到顶板为:斑铜矿→辉铜矿→黄铜矿→黄铁矿,具有典型的化学沉积成因铜的硫化物排列组合特征.这些特点与中国及国外海相砂页岩型铜矿相一致.     

Mesozoic and cenozoic sandstone-hosted copper deposits in south China

Mesozoic and Cenozoic sandstone-hosted copper deposits in South China are confined to the variegated rock formation of the faulted basins, the intermontane basins and piedmont basins around a copper-bearing old land. The variegated rock formation is generally of fluviolacustrine delta facies, shore facies and shore-cauce facies. The ore bodies are stratiform, occurring in the light-coloured beds of the variegated rock formation. The mineralization comprises chalcocite, bornite, chalcopyrite, native copper, covellite, pyrite and hematite, showing obvious zonation. The associated profitable elements in the ore are mainly silver, lead, zinc, molybdenum, selenium and uranium. The copper deposits are believed to have been formed through three processes of enrichment, i.e. weathering (copper-bearing weathered crust was formed as a result), deposition (source bed formed) and diagenesis (ore body formed). The variegated rocks with Cu, Ag, Pb, Zn, U, Mo, Cl and organic carbon anormalies and a great deal of pyrite, distributed in the faulted basins around the Cu-bearing old land, are recognized as the most favourable area for copper ore exploration.     

Mineralogy, Geochemistry, Fluid Inclusion and Oxygen Isotope Investigations of Epithermal Cu ± Ag Veins of the Khur Area, Lut Block, Eastern Iran

The Khur metallogenic district is located in a volcanic-plutonic belt in the central Lut Block(central eastern Iran). Mineralization occurs in Middle Eocene andesitic tuff and along four main vein systems trending northwest-southeast(Shurk, Mir-e-Khash, Shikasteh Sabz and Ghar-e-Kaftar veins).Microscopic studies reveal that the veins contain bornite, chalcocite, pyrite, tennantite together with minor sphalerite and chalcopyrite as hypogene minerals and chalcocite, digenite, covellite, valleriite,malachite, azurite, atacamite, hematite, and goethite as supergene minerals. The ore bodies are accompanied by narrow but intensely developed wall rock alterations of argillization, carbonatization and silicification. Copper content reaches 6.5, 2.4, 4.2 and 5% in Mir-e-Khash, Shikasteh Sabz, Ghar-eKaftar and Shurk, respectively. Microthermometric measurements of quartz-and calcite-hosted fluid inclusions indicate that the mineralization might be derived from a moderately saline hydrothermal fluid at temperatures between 175-316℃. Calculated δ~(18)O values of water in equilibrium with quartz and calcite for Khur veins suggest that the fluid might have had a magmatic source, but the ~(18)O-depletion was developed through mixing with meteoric water. Copper deposition in Khur veins is believed to have been largely caused by mixing, although wall rock reactions may also have occurred. The Khur veins are classified as volcanic-subvolcanic hydrothermal-related vein deposits.     

紫金山金铜矿床深部成矿作用研究和找矿前景评价的关键

紫金山铜金矿床是典型的高硫化浅成低温热液矿床, 发育巨厚的热液蚀变帽, 多孔状石英和高级泥化蚀变带等标志性特征; 特别是在金矿体之下出现垂直厚度超过1000米的巨大铜矿体, 属于蓝辉铜矿－铜蓝－硫砷铜矿－明矾石矿物组合的高硫化型浅成低温热液铜矿床类型, 铜硫化物的矿物学研究预示着深部可能变为斑岩型铜矿床。     

Fluid Inclusion Study and Opaque Mineral Assemblage at the Deep and Shallow Part of the Batu Hijau Porphyry Copper-gold Deposit, Sumbawa, Indonesia

The Batu Hijau deposit is the only porphyry type deposit in production in the Sunda‐Banda arc, Indonesia. This study discusses the reason for the localization of copper grade at the deep part of the deposit based on the observation of opaque mineral assemblage. In addition, the formation condition of quartz veins and opaque minerals is discussed on the basis of the fluid inclusion microthermometry. Samples were selected from drill holes SBD100, SBD168, SBD194, SBD254, and SBD257 to cover the wide vertical range. At the Batu Hijau deposit, quartz veins have been classified mainly into four types called A, B, C and D veins, and the A veins contain mainly bornite, often associated with digenite and chalcocite. In addition, magnetite occurs in A veins. However, at the deep part of the deposit, there are quartz veins associated with magnetite, but few copper sulfides such as bornite and chalcopyrite in quartz veins, as observed in SBD257. Quartz veins at depth in SBD257 have abundant magnetite and pyrite. Pyrite in quartz veins at depth in SBD257 mainly occur at the rim of magnetite grains or interstices between them. In quartz veins in SBD254, there are abundant copper sulfides such as bornite and chalcopyrite in spite of the depth. Bornite and chalcopyrite occur as inclusions in magnetite grains in quartz veins in SBD254. Pyrite which often occurs in low grade zone in quartz veins in SBD254 is also recognized at the rims of copper sulfides. This indicates that pyrite in SBD257 and SBD254 formed later than magnetite. On the other hand, blebs of bornite and chalcopyrite inclusions in magnetite grains, which are recognized in quartz veins in SBD168 at shallow high grade part, suggest that the hydrothermal fluid, from which magnetite was deposited also brought the copper sulfides such as bornite and chalcopyrite to the deep part of the Batu Hijau deposit. Therefore, it is concluded that initially the high grade ore zone extended to depth without localization. However due to the later overprinting hydrothermal activity, copper sulfides and magnetite were replaced or dissolved and pyrite was formed, resulting the low grade zone at the deep part of the deposit. Dissolution temperatures (Td) of halite obtained by from fluid inclusion microthermometry show significant differences between SBD168 and other drill holes. The high Td obtained in SBD168 may indicate larger volume of NaCl crystals in hydrothermal fluid at the time of entrapment of the fluid inclusions and formation of other opaque minerals such as magnetite and copper‐iron sulfides. It suggests that the ratio of vapor to brine is also higher at the shallow part of the deposit. The higher vapor to brine ratio may suggest a higher degree of boiling. Removal of vapor phase separated from brine during boiling increases the concentration of substances dissolved in the brine, and this will result in saturation, as evidenced by the salinity and NaCl saturation. The higher degree of boiling suggested by the higher vapor to brine ratio at shallow part may have increased the copper concentration in the brine that may have lead the saturation, resulted in the deposition of copper‐bearing minerals.     

Mineralogical and Genetical Aspects of the Doyashiki Kuroko Deposits, Hokuroku Basin, Japan

Abstract. A detail investigation of ore and gangue minerals was performed on the Doyashiki Kuroko deposits, Hokuroku basin, Japan for the first time. Main ore minerals are sphalerite, galena, pyrite, chalcopyrite, tetrahedrite-tennantite and digen-ite. Small amounts of enargite, wittichenite, electrum, covellite, bornite, marcasite and hematite are also observed. Quartz, barite and gypsum are common gangue minerals. Homogenization temperatures and salinities of fluid inclusions in quartz, sphalerite and barite range from 190 to 240C and 3.0 to 5.5 wt% NaCl equivalent, respectively. The FeS contents of sphalerite and Ag contents of electrum were 0.12 to 0.18 mol %, 39.0 to 39.6 atom %, respectively. The chemical composition of digenite as a primary mineral shows high sulfur contents.
These data indicate that ore fluid responsible for digenite and associated ore minerals was characterized by a range of high sulfur fugacity with a moderate formation temperature. This is concordant with the mineral assemblage of bornite-pyrite and chalcopyrite, which shows high sulfur fugacity conditions. It seems that the mineralization closely associated with acidic volcanism has occurred around 13 Ma of Middle Miocene on the seafloor at the depth of about 1500 m.     

Supergene sulphides and related minerals in the supergene profiles of VHMS deposits from the South Urals

The mineralogy and structure of the supergene profile in recently-exploited volcaniс hosted massive sulphide (VHMS) deposits of Cyprus, Uralian and Kuroko type in the South Urals, Russia, have been studied. Specific subzones enriched in secondary sulphides and associated minerals have been distinguished in residual pyrite and quartz–pyrite sands at the Gayskoye, Zapadno-Ozernoye, Dzhusinskoye and Alexandrinskoye deposits. Besides minerals which are common to the cementation subzones (covellite, chalcocite and acanthite), non-stoichiometric colloform and framboidal pyrite, pyrite–dzharkenite, pyrrhotite-like and jordanite-like minerals, metacinnabar, sphalerite, selenium-enriched tetrahedrite and unidentified As-, Sb sulphosalts of Pb or Hg and Ag, sulphur-bearing clausthalite, naumannite and tiemannite were also found. Secondary sulphide minerals in VHMS deposits of the South Urals region are characterized by light sulphur isotope compositions (− 8.1 to − 17.2‰). Superposition of the advanced oxidation of colloform pyrite, an enrichment in impurities (sphalerite, galena, and tennantite) from the primary ores, stagnant water conditions, an elevation of the water table during oxidation, and bacterial activity led to supergene concentrations of the base metals as sulphide, selenides or sulphosalts.     

福建紫金山铜金矿床中的完整Cu-S体系矿物

在电子探针微区化学成分分析的基础上,结合 X 射线粉末衍射分析,对福建紫金山铜金矿床中的 Cu-S 体系矿物进行 了化学成分和晶体结构特征的研究。结果在该矿床中发现较完整的 Cu-S 体系矿物系列,包括铜蓝、雅硫铜矿、斯硫铜矿、 吉硫铜矿、斜方蓝辉铜矿、蓝辉铜矿、久辉铜矿和辉铜矿。此外,利用粉末 X 射线衍射数据,计算了铜蓝、斜方蓝辉铜矿、 蓝辉铜矿、久辉铜矿、辉铜矿等五种矿物的晶胞参数。基于系统矿物学的研究,建立了紫金山铜金矿床 Cu-S 体系完整矿物 的结晶与变化序列,该工作在国内尚属首次,同时也丰富了 Cu-S 体系矿物基础矿物学研究的资料。     

Experimental replacement of chalcopyrite by bornite: Textural and chemical changes during a solid-state process

Chalcopyrite was reacted with covellite and with chalcocite, respectively, between 200°C and 500°C. The ensuing solid-state replacement of chalcopyrite by bornite was studied both texturally and chemically. The relatively oxidizing conditions of the reaction chalcopyrite+covellite result in massive replacement, lacking structural control, where bornite and pyrite form complex intergrowth textures in chalcopyrite. Bornite nucleates around growing pyrite aggregates because of the release of copper and a decrease in volume. Diffusion of sulphur along grain boundaries and fractures largely controls the textural development. Reaction under the relatively reducing conditions involving chalcopyrite+chalcocite results in replacement of chalcopyrite in the sequence where chalcopyrite is replaced by bornite, below about 355°C, and by intermediate solid solution (ISS) and later bornite, above 355°C. The textural development, changing from replacement, apparently uninfluenced by directional properties in the host, to semioriented replacement, is structurally controlled. This suggests that the process is governed by diffusion of copper and iron through a sulphur framework. It is suggested that the observed formation of oriented bornite lamellae in chalcopyrite and in ISS during the chalcopyrite+chalcocite reaction may be explained by replacement exsolution at constant temperature.     

Redbed-type gold mineralisation, Kupferschiefer, south-west Poland

A new type of gold mineralisation containing minor amounts of platinum and palladium has been found proximal to the secondary redox interface located below the Cu-Ag Kupferschiefer orebody of the Polkowice-Sieroszowice mine in the south-western part of the Lubin-Sieroszowice district, Poland. This deposit can be classified as redbed-type gold. Our study shows that gold, platinum and palladium occur in secondary red-coloured sections of the basal Zechstein sedimentary rocks and in the uppermost Weissliegendes sandstone. Noble metal mineralisation occurs within an average interval of 0.22 m, which lies directly below the copper ores. The average grade of the horizon is 2.25 ppm Au, 0.138 ppm Pt and 0.082 ppm Pd with a metal content of several tens of tonnes of gold. A transition zone has been recognised between the gold-bearing horizon and the copper deposit. This transition zone is characterised by the presence of low grades of copper (<0.2 wt%) and elevated gold contents (>0.5 ppm). Native gold accompanied by electrum, mercury-bearing gold, haematite, covellite, chalcocite, bornite and chalcopyrite has been identified in the gold-bearing horizon. In some sections, Pd-arsenides, tetra-auricupride, Co-arsenides, clausthalite, tennantite, digenite, yarrowite, spionkopite and galena have also been noted.     

Geochemistry and alteration facies associated with epithermal precious metal mineralization in an active geothermal system,northern Lesbos,Greece

Hydrothermal quartz veins associated with gold and silver mineralization and variable amounts of base metal sulfides have been discovered within an active geothermal system in the Megala Therma area of northern Lesbos. This geothermal system is probably a late evolutionary stage in the formation of this mineralization. The veins are hosted in Upper Miocene volcanic rocks of andesitic composition and consist of quartz, adularia, chlorite, sericite, illite, kaolinite, baryte, small amounts of jarosite and alunite, and native gold, pyrite, galena, sphalerite, chalcopyrite, bornite, chalcocite, covellite and goethite. The principal types of alteration which occur in the studied area are: silicification, propylitization, argillic alteration and potassic, phyllic alteration.     

刚果（金）如瓦西铜-钴矿床表生成矿过程及其勘探意义

中非成矿带刚果（金）如瓦西（Ruashi）铜-钴矿床经历了表生成矿作用,但其研究薄弱。在野外地质调查、室内矿物学观察和矿山生产勘探的基础上,对如瓦西铜-钴矿床的表生分带组构与次生富集规律进行研究。结果表明,该矿床原生矿体由黄铜矿、斑铜矿、硫铜钴矿等含铜硫化物矿物组成,矿石品位铜在1%~2%、钴在0.1%~0.3%范围内。矿床在近地表发生表生氧化作用后,上部形成了氧化带,可进一步划分为3个亚带：（1）完全氧化亚带;（2）淋滤亚带;（3）次生氧化物富集亚带。上部完全氧化亚带发育富钴氧化物堆积体“矿帽”（钴品位在1%~3%,部分可达12%）,淋滤亚带几乎不含铜、钴金属矿物,次生富集氧化物亚带由孔雀石、硅孔雀石、蓝铜矿、胆矾、水胆矾等氧化物矿物和碳酸盐矿物组成,矿石品位铜在5%~10%、钴在0.8%~1.0%范围内,相对原生矿石富集了3~5倍。下部为次生硫化物富集带,出现蓝铜矿、辉铜矿等次生硫化物矿物,矿石品位铜在3%~5%、钴在0.3%~0.8%范围内,相对原生硫化矿富集了1~3倍。综合分析认为,如瓦西铜-钴矿床表生成矿作用受岩石地层、地质构造和地下水等因素的控制,次生富集作用明显提高了矿石品位和矿床开发价值,形成了氧化物富铜-钴矿、硫化物富铜-钴矿和碳酸盐岩接触带附近的氧化物富铜矿及黑色富钴矿等类型的高-特高品位矿体。经勘探验证,在矿区深边部新揭露高品位矿石资源量256万吨,平均品位铜为3.68%、钴为0.44%,可采储量143万吨,平均品位铜为3.53%、钴为0.32%。该研究可为矿区及区域同类型矿山硫化矿演化成氧化矿的表生富集过程及深边部找矿预测提供科学依据。     

The Arinem Te‐Bearing Gold‐Silver‐Base Metal Deposit,West Java,Indonesia

The vein system in the Arinem area is a gold‐silver‐base metal deposit of Late Miocene (8.8–9.4 Ma) age located in the southwestern part of Java Island, Indonesia. The mineralization in the area is represented by the Arinem vein with a total length of about 5900 m, with a vertical extent up to 575 m, with other associated veins such as Bantarhuni and Halimun. The Arinem vein is hosted by andesitic tuff, breccia, and lava of the Oligocene–Middle Miocene Jampang Formation (23–11.6 Ma) and overlain unconformably by Pliocene–Pleistocene volcanic rocks composed of andesitic‐basaltic tuff, tuff breccia and lavas. The inferred reserve is approximately 2 million tons at 5.7 g t^?1 gold and 41.5 g t^?1 silver at a cut‐off of 4 g t^?1 Au, which equates to approximately 12.5t of Au and 91.4t of Ag. The ore mineral assemblage of the Arinem vein consists of sphalerite, galena, chalcopyrite, pyrite, marcasite, and arsenopyrite with small amounts of pyrrhotite, argentite, electrum, bornite, hessite, tetradymite, altaite, petzite, stutzite, hematite, enargite, tennantite, chalcocite, and covellite. These ore minerals occur in quartz with colloform, crustiform, comb, vuggy, massive, brecciated, bladed and calcedonic textures and sulfide veins. A pervasive quartz–illite–pyrite alteration zone encloses the quartz and sulfide veins and is associated with veinlets of quartz–calcite–pyrite. This alteration zone is enveloped by smectite–illite–kaolinite–quartz–pyrite alteration, which grades into a chlorite–smectite–kaolinite–calcite–pyrite zone. Early stage mineralization (stage I) of vuggy–massive–banded crystalline quartz‐sulfide was followed by middle stage (stage II) of banded–brecciated–massive sulfide‐quartz and then by last stage (stage III) of massive‐crystalline barren quartz. The temperature of the mineralization, estimated from fluid inclusion microthermometry in quartz ranges from 157 to 325°C, whereas the temperatures indicated by fluid inclusions from sphalerite and calcite range from 153 to 218 and 140 to 217°C, respectively. The mineralizing fluid is dilute, with a salinity <4.3 wt% NaCl equiv. The ore‐mineral assemblage and paragenesis of the Arinem vein is characteristically of a low sulfidation epithermal system with indication of high sulfidation overprinted at stage II. Boiling is probably the main control for the gold solubility and precipitation of gold occurred during cooling in stage I mineralization.     

Primary Ore Mineral Assemblage and Fluid Inclusion Study of the Batu Hijau Porphyry Cu-Au Deposit, Sumbawa, Indonesia

Abstract. The Batu Hijau porphyry Cu‐Au deposit, Sumbawa Island, Indonesia, is associated with a tonalitic intrusive complex. The temperature‐pressure condition of mineralization at the Batu Hijau deposit is discussed on the basis of fluid inclusion microthermometry. Then, the initial Cu‐Fe sulfide mineral assemblage is discussed. Bornite and chalcopyrite are major copper ore minerals associated with quartz veinlets. The quartz veinlets have been classified into ‘A’ veinlets associated with bornite, digenite, chalcocite and chalcopyrite, ‘B’ veinlets having chalcopyrite bornite along vuggy center‐line, rare ‘C’ chalcopyrite‐quartz veinlets, and late ‘D’ veinlets consisting of massive pyrite and quartz (Clode et al., 1999). Copper and gold mineralization is associated with abundant ‘A’ quartz veinlets. Abundant fluid inclusions are found in veinlet quartz consisting mainly of gas‐rich inclusions and polyphase inclusions throughout the veinlet types. The hydrothermal activity occurred in temperature‐pressure conditions of aqueous fluid immiscibility into hypersaline brine and dilute vapor. The halite dissolution (Tm[halite]) and liquid‐vapor homogenization (Th) temperatures of the polyphase inclusions in veinlet quartz range from 270 to 472d?C and from 280 to 454d?C, respectively. The estimated salinity ranges from 36 to 47 wt% (NaCl equiv.). The apparent pressures lower than 300 bars are estimated to have been along the liquid‐vapor‐halite curve for the fluid inclusions having the Th lower than the Tm that trapped the brine saturated with halite, or at slightly higher pressure relative to liquid‐vapor‐halite curve for the fluid inclusions having the Th higher than the Tm that trapped the brine unsaturated with halite. The actual temperature and pressure during the hydrothermal activity at the Batu Hijau deposit are estimated to have been around 300d?C and 50 bars. At such temperature‐pressure conditions, the principal and initial Cu‐Fe sulfide mineral assemblages are thought to be chalcopyrite + bornite solid solution (bnss) for the chalcopyrite‐bearing assemblage, and chalcocite‐digenite solid solution and bnss for the chalcopyrite‐free assemblage.     

Geology and geochemistry of the sediment-hosted Cheshmeh-Konan redbed-type copper deposit,NW Iran

The several-hundred-m-thick Miocene Upper Red Formation in northwestern Iran hosts stratiform and fault-controlled copper mineralization. Copper enrichment in the percent range occurs in dm-thick carbonaceous sandstone and shale units within the clastic redbed sequence and consists of fine-grained disseminated copper sulfides (chalcopyrite, bornite, chalcocite) and supergene alteration minerals (covellite, malachite and azurite). The copper mineralization formed after calcite cementation of the primary rock permeability. Copper sulfides occur mainly as replacement of diagenetic pyrite, which, in turn, replaced organic matter. Electron microprobe analysis on bornite, chalcocite and covellite identifies elevated silver contents in these minerals (up to 0.12, 0.72 and 1.21 wt%, respectively), whereas chalcopyrite and pyrite have only trace amounts of silver (<0.26 and 0.06 wt%, respectively). Microthermometric data on fluid inclusions in authigenic quartz and calcite indicate that the Cu mineralization is related to a diagenetic fluid of moderate-to low temperature (Th = 96–160 °C) but high salinity (25–38 wt% CaCl₂ equiv.). The range of δ³⁴S in pyrite is −41.9 to −16.4‰ (average −31.4‰), where framboidal pyrite shows the most negative values between −41.9 and −31.8‰, and fine-grained pyrite has relatively heavier δ³⁴S values (−29.2 to −16.4‰), consistent with a bacteriogenic derivation of the sulfur. The Cu-sulfides (chalcopyrite, bornite and chalcocite) show slightly heavier values from −14.6 to −9.0‰, and their sulfur sources may be both the precursor pyrite-S and the bacterial reduction of sulfate-bearing basinal brines. Carbonates related to the ore stage show isotopically light values of δ¹³C_V-PDB from −8.2 to −5.1‰ and δ¹⁸O_V-PDB from −10.3 to −7.2‰, indicating a mixed source of oxidation of organic carbon (ca. −20‰) and HCO₃⁻ from seawater/porewater (ca. 0‰). The copper mineralization is mainly controlled by organic matter content and paleopermeability (intragranular space to large fracture patterns), enhanced by feldspar and calcite dissolution. The Cheshmeh-Konan deposit can be classified as a redbed-type sediment-hosted stratiform copper (SSC) deposit.     

The geochemistry of gossans associated with Sarcheshmeh porphyry copper deposit,Rafsanjan, Kerman,Iran: Implications for exploration and the environment

The Sarcheshmeh copper deposit is one of the world's largest Oligo-Miocene porphyry copper deposits in a continental arc setting with a well developed supergene sulfide zone, covered mainly by a hematitic gossan. Supergene oxidation and leaching, have developed a chalcocite enrichment blanket averaging 1.99% Cu, more than twice that of hypogene zone (0.89% Cu). The mature gossans overlying the Sarcheshmeh porphyry copper ores contain abundant hematite with variable amounts of goethite and jarosite, whereas immature gossans consist of iron-oxides, malachite, azurite and chrysocolla. In mature gossans, Au, Mo and Ag give significant anomalies much higher than the background concentrations. However, Cu has been leached in mature gossans and gives values close or even less than the normal or crustal content (< 36.7 ppm). Immature gossans are enriched in Cu (160.3 ppm), Zn (826.7 ppm), and Pb (88.6 ppm). Jarosite- and goethite-bearing gossans may have developed over the pyritic shell of most Iranian porphyry copper deposits with pyrite–chalcopyrite ratios greater than 10 and therefore, do not necessarily indicate a promising sulfide-enriched ore (Kader and Ijo). Hematite-bearing gossans overlying nonreactive alteration halos with pyrite–chalcopyrite ratios about 1.5 and quartz stringers have significant supergene sulfide ores (Sarcheshmeh and Miduk). The copper grade in supergene sulfide zone of Sarcheshmeh copper deposit ranges from 0.78% in propylitized rocks to 3.4% in sericitized volcanic rocks, corresponding to the increasing chalcopyrite–pyrite or chalcocite–pyrite ratios from 0.3 to 3, respectively. Immature gossans with dominant malachite and chrysocolla associated with jarosite and goethite give the most weakly developed enrichment zone, as at God-e-Kolvari. The average anomalous values of Au (59.6 ppb), Mo (42.5 ppm) and Ag (2.6 ppm) in mature gossans associated with the Sarcheshmeh copper mine may be a criterion that provides a significant exploration target for regional metallogenic blind porphyry ore districts in central Iranian volcano–plutonic continental arc settings. Drilling for new porphyry ores should be targeted where hematitic gossans are well developed. The ongoing gossan formation may result in natural acidic rock drainage (ARD).     

Remobilization of gold from a chalcopyrite-pyrite mineralization Hamash gold mine,Southeastern Desert,Egypt

Pyrite, chalcopyrite, and gold occur in quartz veins in granitic rocks and as scattered and disseminated impregnations in shear zones of the highly altered metavolcanics in the Hamash area, Southeastern Desert, Egypt. The minerals are associated in part with pyrrhotite, digenite, tetrahedrite, chalcocite, bornite, and covellite. Pyrite occurs in two forms: (1) idio- to hypidiomorphic coarse crystals with inclusions of preexisting sulfides, and (2) fine-crystalline aggregates. Chalcopyrite occurs in three forms: (1) idiomorphic coarse crystals, (2) fine-crystalline microinclusions, and (3) xenomorphic relicts. Three genetic phases of sulfide mineralization were identified. They are related to the successive cooling of the crystallizing solutions. Gold was hosted in the older sulfide minerals during a high-temperature disorder phase. Native gold was formed during the latest, decreasing-temperature phase through remobilization of auriferous pyrite. Microprobe analysis confirmed that gold and copper are relatively enriched in the late pyrite. Identified surface-alteration products include goethite, limonite, gold, carbonates, and sulfates of iron and copper.