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1.
The Southwest prospect is located at the southwestern periphery of the Sto. Tomas II porphyry copper–gold deposit in the Baguio District, northwestern Luzon, Philippines. The Southwest prospect hosts a copper‐gold mineralization related to a complex of porphyry intrusions, breccia facies, and overlapping porphyry‐type veinlets emplaced within the basement Pugo metavolcanics rocks and conglomerates of the Zigzag Formation. The occurrences of porphyry‐type veinlets and potassic alteration hosted in the complex are thought to be indications of the presence of blind porphyry deposits within the Sto. Tomas II vicinity. The complex is composed of at least four broadly mineralogically similar dioritic intrusive rocks that vary in texture and alteration type and intensity. These intrusions were accompanied with at least five breccia facies that were formed by the explosive brecciation, induced by the magmatic–hydrothermal processes and phreatomagmatic activities during the emplacement of the various intrusions. Hydrothermal alteration assemblages consisting of potassic, chlorite–magnetite, propylitic and sericite–chlorite alteration, and contemporaneous veinlet types were developed on the host rocks. Elevated copper and gold grades correspond to (a) chalcopyrite–bornite assemblage in the potassic alteration in the syn‐mineralization early‐mineralization diorite (EMD) and contemporaneous veinlets and (b) chalcopyrite‐rich mineralization associated with the chalcopyrite–magnetite–chlorite–actinolite±sericite veinlets contemporaneous with the chlorite–magnetite alteration. Erratic remarkable concentrations of gold were also present in the late‐mineralization Late Diorite (LD). High XMg of calcic amphiboles (>0.60) in the intrusive rocks indicate that the magmas have been oxidizing since the early stages of crystallization, while a gap in the composition of Al between the rim and the cores of the calcic amphiboles in the EMD and LD indicate decompression at some point during the crystallization of these intrusive rocks. Fluid inclusion microthermometry suggests the trapping of immiscible fluids that formed the potassic alteration, associated ore mineralization, and sheeted quartz veinlets. The corresponding formation conditions of the shallower and deeper quartz veinlets were estimated at pressures of 50 and 30 MPa and temperatures of 554 and 436°C at depths of 1.9 and 1.1 km. Temperature data from the chlorite indicate that the chalcopyrite‐rich mineralization associated with the chlorite–magnetite alteration was formed at a much lower temperature (ca. 290°C) than the potassic alteration. Evidence from the vein offsetting matrix suggests multiple intrusions within the EMD, despite the K‐Ar ages of the potassic alteration in EMD and hornblende in the LD of about the same age at 3.5 ± 0.3 Ma. The K‐Ar age of the potassic alteration was likely to be thermally reset as a result of the overprinting hydrothermal alteration. The constrained K‐Ar ages also indicate earlier formed intrusive rocks in the Southwest prospect, possibly coeval to the earliest “dark diorite” intrusion in the Sto. Tomas II deposit. In addition, the range of δ34S of sulfide minerals from +1.8‰ to +5.1‰ in the Southwest prospect closely overlaps with the rest of the porphyry copper and epithermal deposits in the Sto. Tomas II deposit and its vicinity. This indicates that the sulfides may have formed from a homogeneous source of the porphyry copper deposits and epithermal deposits in the Sto. Tomas II orebody and its vicinity. The evidence presented in this work proves that the porphyry copper‐type veinlets and the adjacent potassic alteration in the Southwest prospect are formed earlier and at a shallower level in contrast with the other porphyry deposits in the Baguio District.  相似文献   

2.
Abstract. Evolution of hydrothermal system from initial porphyry Cu mineralization to overlapping epithermal system at the Dizon porphyry Cu‐Au deposit in western central Luzon, Zambales, Philippines, is documented in terms of mineral paragen‐esis, fluid inclusion petrography and microthermometry, and sulfur isotope systematics. The paragenetic stages throughout the deposit are summarized as follows; 1) stockwork amethystic quartz veinlets associated with chalcopyrite, bornite, magnetite and Au enveloped by chlorite alteration overprinting biotite alteration, 2) stockwork quartz veinlets with chalcopyrite and pyrite associated with Au and chalcopyrite and pyrite stringers in sericite alteration, 3) stringer quartz veinlets associated with molybdenite in sericite alteration, and 4) WNW‐trending quartz veins associated with sphalerite and galena at deeper part, while enargite and stibnite at shallower levels associated with advanced argillic alteration. Chalcopyrite and bornite associated with magnetite in quartz veinlet stockwork (stage 1) have precipitated initially as intermediate solid solution (iss) and bornite solid solution (bnss), respectively. Fluid inclusions in the stockwork veinlet quartz consist of gas‐rich inclusions and polyphase inclusions. Halite in polyphase inclusions dissolves at temperatures ranging from 360d?C to >500d?C but liquid (brine) and gas (vapor) do not homogenize at <500d?C. The maximum pressure and minimum temperature during the deposition of iss and bnss with stockwork quartz veinlets are estimated to be 460 bars and 500d?C. Fluid inclusions in veinlet stockwork quartz enveloped in sericite alteration (stage 2) consist mainly of gas‐rich inclusions and polyphase inclusions. In addition to the possible presence of saturated NaCl crystals at the time of entrapment of fluid inclusions that exhibit the liquid‐vapor homogenization temperatures lower than the halite dissolution temperatures in some samples, wide range of temperatures of halite dissolution and liquid‐vapor homogenization of polyphase inclusions from 230d?C to >500d?C and from 270d?C to >500d?C, respectively, suggests heterogeneous entrapment of gaseous vapor and hypersaline brine. The minimum pressure and temperature are estimated to be about 25 bars and 245d?C. Fluid inclusions in veinlet quartz associated with molybdenite (stage 3) are dominated by gas‐rich inclusions accompanied with minor liquid‐rich inclusions that homogenize at temperatures between 350d?C and 490d?C. Fluid inclusions in vuggy veinlet quartz associated with stibnite (stage 4) consist mainly of gas‐rich inclusions with subordinate polyphase inclusions that do not homogenize below 500d?C. Fluid inclusions in veinlet quartz associated with galena and sphalerite (stage 4) are composed of liquid‐rich two‐phase inclusions, and they homogenize into liquid phase at temperatures ranging widely from 190d?C to 300d?C (suggesting boiling) and the salinity ranges from 1.0 wt% to 3.4 wt% NaCl equivalent. A pressure of about 15 bars is estimated for the dilute aqueous solution of 190d?C from which veinlet quartz associated with galena and sphalerite precipitated. In addition to a change in temperature‐pressure regime from lithostatic pressure during the deposition of iss and bnss with stockwork quartz veinlets to hydrostatic pressure during fracture‐controlled quartz veinlet associated with galena and sphalerite, a decrease in pressure is supposed to have occurred due to unroofing or removal of the overlying piles during the temperature decrease in the evolution of hydrothermal system. The majority of the sulfur isotopic composition of sulfides ranges from ±0 % to +5 %. Sulfur originated from an iso‐topically uniform and homogeneous source, and the mineralization occurred in a single hydrothermal system.  相似文献   

3.
The Miduk porphyry copper deposit is located in Kerman province, 85 km northwest of the Sar Cheshmeh porphyry copper deposit, Iran. The deposit is hosted by Eocene volcanic rocks of andesitic–basaltic composition. The porphyry‐type mineralization is associated with two Miocene calc‐alkaline intrusive phases (P1 and P2, respectively). Five hypogene alteration zones are distinguished at the Miduk deposit, including magnetite‐rich potassic, potassic, potassic–phyllic, phyllic and propylitic. Mineralization occurs as stockwork, dissemination and nine generations (magnetite, quartz–magnetite, barren quartz, quartz‐magnetite‐chalcopyrite‐anhydrite, chalcopyrite–anhydrite, quartz‐chalcopyrite‐anhydrite‐pyrite, quartz‐molybdenite‐anhydrite ± chalcopyrite ± magnetite, pyrite, and quartz‐pyrite‐anhydrite ± sericite) of veinlets and veins. Early stages of mineralization consist of magnetite rich veins in the deepest part of the deposit and the main stage of mineralization contains chalcopyrite, magnetite and anhydrite in the potassic zone. The high intensity of mineralization is associated with P2 porphyry (Miduk porphyry). Based on petrography, mineralogy, alteration halos and geochemistry, the Miduk porphyry copper deposit is similar to those of continental arc setting porphyry copper deposits. The Re‐Os molybdenite dates provide the timing of sulfide mineralization at 12.23 ± 0.07 Ma, coincident with U/Pb zircon ages of the P2 porphyry. This evidence indicates a direct genetic relationship between the Miduk porphyry stock and molybdenite mineralization. The Re‐Os age of the Miduk deposit marks the main stage of magmatism and porphyry copper formation in the Central Iranian volcano‐plutonic belt.  相似文献   

4.
The porphyry Cu deposits at Waisoi in Namosi district, Viti Levu are separated into two deposits: the Waisoi East deposit and the Waisoi West deposit. In the Waisoi East deposit, quartz porphyry is exposed and in the Waisoi West deposit, diorite porphyry is sporadically exposed in addition to a small body of quartz porphyry. The mineralization in the Waisoi East deposit is characterized by the bornite–chalcopyrite–pyrite assemblage associated with traces of molybdenite and native gold. Polyphase fluid inclusions in stockwork quartz veinlets show homogenization temperatures ranging from 210 to >500°C. The high‐grade Cu mineralization in the Waisoi West deposit is characterized by the bornite–chalcopyrite–pyrite assemblage accompanied with sheeted and stockwork quartz veinlets. Polyphase fluid inclusions occasionally containing hematite flakes in quartz veinlets in the center of the Waisoi West deposit homogenize at temperatures ranging from 450°C to >500°C. However, fluid inclusions in stockwork quartz veinlets in the periphery, homogenize at lower temperatures around 210°C. Both in the Waisoi East and Waisoi West deposits, primary bornite–chalcopyrite–pyrite assemblage in the high Cu‐grade zone was deposited at the upper stability limit of chalcopyrite with respect to sulfur fugacity. Thus, the principal Cu mineralization at the Waisoi deposits occurred at a relatively high sulfur fugacity, that is, in a high‐sulfidation environment.  相似文献   

5.
The Kingking deposit is a gold‐rich porphyry copper deposit and the southernmost deposit at the eastern Mindanao mineralized belt, Philippines. It is underlain by Cretaceous–Paleogene sedimentary and volcanic rocks that are intruded by mineralized Miocene diorite porphyries and by barren Miocene–Pliocene dacite and diorite porphyries. The main alteration zones in the deposit are the inner potassic zone and the outer propylitic zone. The biotite‐bearing diorite and hornblende diorite porphyries are the primary host rocks of mineralization. Two dominant copper minerals, bornite and chalcopyrite, which usually occur as fracture fillings, are associated with fine crystalline quartz veinlet stockworks in the mineralized diorites. Minor secondary covellite, chalcocite and digenite are also observed. The primary Cu‐Fe sulfide phases initially deposited from ore fluids consisted of bornite solid solution (bnss) and intermediate solid solution (iss), which decomposed to form the bornite and chalcopyrite. Peculiar bornite pods that are different from dissemination and are associated with volcanic rock xenoliths in biotite‐bearing diorite porphyry are noted in a drill hole. These pods of bornite are not associated with quartz veinlet stockworks. Fluid inclusion analyses show three types of inclusions contained in Kingking samples: two‐phase fluid‐rich and vapor‐rich inclusions and polyphase hypersaline inclusions from porphyry‐type quartz veinlet stockworks. The liquid–vapor homogenization temperatures (TH) and the dissolution temperature of halite daughter crystals (TM) from the polyphase hypersaline inclusions predominantly range from 400°C up to >500°C. The wide range of TH and TM may be due to heterogeneous trapping of variable ratios of vapor and brine. For some inclusions, TH > TM and in some cases, TH < TM, indicating that some of the brine was supersaturated or saturated with NaCl at the time of entrapment. Calculated salinity of the polyphase hypersaline inclusions ranges from 40 to 60% NaCl equivalent. Temperature and vapor pressure of mineralized fluid were estimated to be 400°C and 16 MPa.  相似文献   

6.
The Selogiri area, situated in Wonogiri regency, Central Java, is one of several gold prospecting areas in the Southern areas Mountain Range in Java, Indonesia. Three types of dioritic–andesitic intrusive rocks occur in the Selogiri area, namely, hornblende andesite porphyry, hornblende diorite porphyry and hornblende diorite, exposed in a half‐circular depression where volcanic breccia and tuff are widely distributed. The occurrence of stockwork quartz veinlets and associated with magnetite and malachite coating along the cracks in the diorite porphyry suggests porphyry type mineralization. This is also supported by the occurrence of polyphase hypersaline fluid inclusions in the stockwork veinlet quartz. Small‐scale miners are mining NS‐trending quartz veins for gold associated with base metal sulfides. These veins are probably epithermal‐type mineralization that overprinted porphyry‐type mineralization. The Neogene intermediate to silicic hydrous magmatism in Java could have formed the porphyry‐type mineralization in Selogiri, as in the rest of the Sunda–Banda arc.  相似文献   

7.
Abstract: The Lepanto Far Southeast porphyry Cu‐Au deposit is located beneath and to the southeast of the Lepanto enargite‐luzonite Cu–Au deposit in Mankayan, Benguet Province, Philippines. The principal orebody consists of potassic alteration subjected to partial retrograde chlorite alteration that rims stock‐work of quartz‐anhydrite veinlets. Fluid inclusions found in stockwork quartz and anhydrite in the biotitized orebody center are dominated by polyphase inclusions that homogenize at temperatures of >500C. Sulfur isotopic thermometry applied to the sulfides‐anhydrite pairs suggests around 500C. The principal ore minerals associated with quartz‐anhydrite stockworks are chalcopyrite and pyrite with minor bornite and Bi–Te–bearing tennantite, with trace of native gold. Rounded pyrite grains appear fractured and corroded and are interpreted as remnants of primary intermediate solid solution + pyrite assemblage. A breccia pipe truncates the deposit. Mineralization in the breccia pipe is brought by quartz‐anhydrite veinlets and infilling in the interstices between clasts. Chalcopyrite‐Au mineralization associated with molybdenite is recognized in the deeper zone in the breccia pipe. Fluid inclusion microthermometry on polyphase inclusions in veinlet quartz as well as sulfur isotope thermometry applied for the pair of anhydrite and sulfides suggests >450C. Fluid inclusions in veinlet quartz and anhydrite in the fringe advanced argillic alteration are chiefly composed of coexisting liquid‐rich inclusions and gas‐rich inclusions, in addition to coexisting polyphase inclusions and gas‐rich inclusions. These inclusions exhibit a wide range of homogenization temperatures, suggesting heterogeneous entrapping in the two‐fluid unmixing region. Sulfur isotopes of aqueous sulfide and sulfate exhibit a general trend from the smallest fractionation pairs (about 11%) in the biotitized orebody center to the largest fractionation (about 25%) pairs in the fringe advanced argillic alteration, suggesting a simple evolution of hydrothermal system. The slopes of arbitrary regression lines in δ34S versus 34S[SO4 = –H2S] diagram suggest that the abundance ratio of aqueous sulfate to sulfide in the hydrothermal fluid has been broadly constant at about 1:3 through temperature decrease. The intersection of these two regression lines at the δ34S axis indicates that the bulk δ34S is about +6%. Thus, the Lepanto FSE deposit is a further example which confirms enrichment in 34S in the hydrous intermediate to silicic magmas and associated magmatic hydrothermal deposits in the western Luzon arc.  相似文献   

8.
At the Kingking porphyry copper-gold deposit, Compostela Valley, south-eastern Mindanao, Philippines, bornite pods occur in the brecciated parts in the biotite diorite porphyry, together with the volcanic rock and diorite fragments without associated stockworks of quartz veinlets. These pods are generally elongated in shape and measure several centimeters across their longest axes. They are composed of bornite and chalcopyrite with traces of calaverite. The δ34S of bornite and subordinate chalcopyrite of bornite pods ranging from −2.2‰ to +0.1‰ are similar to the δ34S of sulfides associated with quartz veinlets such as bornite and chalcopyrite ranging from −4.7‰ to ±0.0‰. This suggests that the ultimate source of sulfur is identical for bornite pods and sulfides associated with quartz veinlets. Bornite pods are associated with volcanic rock and dioritic fragments in the brecciated portion of the biotite diorite porphyry. It was observed that some dioritic fragments contain quartz veinlets, which may indicate an earlier episode of mineralization. Fragments of the earlier dioritic intrusive rocks and the volcanic rocks, together with the sulfides were incorporated into the biotite diorite porphyry magma. A molten sulfide is possible for the composition between bornite and intermediate solid solution at ∼800°C. The sulfides from the earlier dioritic intrusive rocks in the molten state were segregated and then eventually coalesce to form the bornite pods in the brecciated section of the biotite diorite porphyry.  相似文献   

9.
Mineralized quartz diorites of the Santo Tomas II porphyry copper-gold deposit, carry high Au contents (average: 1.8 ppm) as well as 160 ppb Pd and 38 ppb Pt. Values of other platinum-group elements (PGE) and rhenium are below the analytical detection limits. There is a significant positive correlation between Au and Cu. The highest Pd values were detected in the most Au- and Cu-rich rocks. Platinum-group minerals (PGM) occur exclusively as inclusions in chalcopyrite and bornite. Potential Pd and Pt contents in sulphide concentrates are estimated at 1.5 g/t and 0.4 g/t, respectively. The precious metal assemblages consist of merenskyite (main PGM), kotulskite, moncheite, native gold, electrum, hessite and petzite. Polyphase fluid inclusions in quartz veinlets, associated with a PGM-bearing bornite-chalcopyrite-magnetite assemblage, are characterized by high salinity (35 to > 60 eq. wt% NaCl) and high trapping temperatures (between 380 and 520 °C). They may represent primary magmatic-hydrothermal fluids, which have been responsible for the transport of Pd, Pt and Au as chloride complexes.  相似文献   

10.
Abstract: The Mamut deposit of Sabah, East Malaysia, is a porphyry type Cu‐Au deposit genetically related to a quartz monzonite (“adamellite”) porphyry stock associated with upper Miocene Mount Kinabalu plutonism. The genesis of the Mamut deposit is discussed based on petrology of the intrusives in the Mount Kinabalu area combined with ore– and alteration–petrography, fluid inclusion and sulfur isotope studies. Groundmass of the adamellite porphyry at Mamut is rich in K which suggests vapor transport of alkaline elements during the mineralizing magmatic process, while the groundmass of the post‐ore “granodiorite” porphyry at Mamut contains small amounts of normative corundum suggesting depletion in alkaline elements at the root zone of the magma column. Sub‐dendritic tremolitic amphibole rims on hornblende phenocrysts in the Mamut adamellite porphyry suggest interaction between the mineralizing magma and the exsolved fluids. Occurrences of clinopyroxene microphenocrysts and pseudomor‐phic aggregates of shredded biotite and clinopyroxene after hornblende phenocrysts in the barren intrusives imply lower water fugacity and decreasing in water fugacity, respectively. Compositional gap between the core of hornblende phenocrysts and the tremolitic amphibole rims and those in the groundmass of the Mamut adamellite porphyry suggests a decrease in pressure. Higher XMg (=Mg/(Mg+Fe) atomic ratio) in the tremolitic amphibole rims in the Mamut adamellite porphyry compared to those of the barren intrusions suggests high oxygen fugacity. High halogen contents of igneous hydrous minerals such as amphiboles, biotite and apatite in the Mamut adamellite porphyry suggest the existence of highly saline fluids during the intrusion and solidification of the mineralizing magma. Fluid inclusions found in quartz veinlet stockworks are characterized by abundant hypersaline polyphase inclusions associated with subordinate amounts of immiscible gaseous vapor. Both Cu and Au are dispersed in disseminated and quartz stockwork ores. Chalcopyrite and pyrrhotite as well as magnetite are the principal ore minerals in the biotitized disseminated ores. Primary assemblage of intermediate solid solution (iss) and pyrrhotite converted to the present assemblage of chalcopyrite and pyrrhotite during cooling. Subsequent to biotitization, quartz veinlet stockworks formed associated with retrograde chlorite alteration. The Cu‐Fe sul–fides associated with stockwork quartz veinlet are chalcopyrite and pyrite. Overlapping Pb and Zn and subsequent Sb mineralizations were spatially controlled by NNE‐trending fractures accompanying the phyllic and advanced argillic alteration envelope. Sulfur isotopic composition of ore sulfides are homogeneous (about +2%) throughout the mineralization stages. These are identical to those of the magmatic sulfides of Mount Kinabalu adamellitic rocks.  相似文献   

11.
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.  相似文献   

12.
Ore mineralization and wall rock alteration of Crater Mountain gold deposit, Papua New Guinea, were investigated using ore and host rock samples from drill holes for ore and alteration mineralogical study. The host rocks of the deposit are quartz‐feldspar porphyry, feldspar‐hornblende porphyry, andesitic volcanics and pyroclastics, and basaltic‐andesitic tuff. The main ore minerals are pyrite, sphalerite, galena, chalcopyrite and moderate amounts of tetrahedrite, tennantite, pyrrhotite, bornite and enargite. Small amounts of enargite, tetradymite, altaite, heyrovskyite, bismuthinite, bornite, idaite, cubanite, native gold, CuPbS2, an unidentified Bi‐Te‐S mineral and argentopyrite occur as inclusions mainly in pyrite veins and grains. Native gold occurs significantly in the As‐rich pyrite veins in volcanic units, and coexists with Bi‐Te‐S mineral species and rarely with chalcopyrite and cubanite relics. Four mineralization stages were recognized based on the observations of ore textures. Stage I is characterized by quartz‐sericite‐calcite alteration with trace pyrite and chalcopyrite in the monomict diatreme breccias; Stage II is defined by the crystallization of pyrite and by weak quartz‐chlorite‐sericite‐calcite alteration; Stage III is a major ore formation episode where sulfides deposited as disseminated grains and veins that host native gold, and is divided into three sub‐stages; Stage IV is characterized by predominant carbonitization. Gold mineralization occurred in the sub‐stages 2 and 3 in Stage III. The fS2 is considered to have decreased from ～10?2 to 10?14 atm with decreasing temperature of fluid.  相似文献   

13.
Dalli Cu–Au porphyry deposit was occurred in the igneous diorite, quartz diorite porphyry (QDP), and volcanic rocks such as porphyritic amphibole andesite, andesite (AND), dacite, and pyroclastics during the late Miocene to Pliocene. Regolith investigations and Advanced Spaceborne Thermal Emission and Reflection Radiometer images were used to identify the anomalous areas. According to lithogeochemical survey (from boreholes and trenches) in Northern Dalli Cu–Au porphyry, the potassic, chlorite, sericite, propylitic, and argillic alterations have been found and mineralization was basically associated with potassic and quartz–sericite alterations. The alteration is dominantly moderate quartz chlorite?±?sericite magnetite with 1–10 mm wide quartz?±?magnetite veinlets. The elevated copper–gold values are correlated with density of stockworking and mineralization. The intensity of the mineralization is high in the contact of QDP and AND with increases in pyrite and chalcopyrite values. Malachite, native Cu, and bornite were used to identify supergene, transition, and hypogene zone. In addition, molybdenum increased near to the center of granodiorite intrusion. And besides, from depth to surface in DDH03 and wall rock to mineralization zones, a sequence of Mo→Cu (Au)→Au (Cu) was recorded and the mineralization temperature cooled down (from high to low). The alteration is characterized by specific pattern and structure in Dalli Cu–Au porphyry deposit. The alteration model was followed from the modified Lowell and Gilbert model. The porphyry is stockworked by quartz veins and by quartz magnetite veins. Vein distribution and ore mineralogy vary between the different alteration zones. Due to the formation of an iron cap in the supergene, especially in the southern hills, supergene grade was higher than hypogene zone. Also, hematite, as a dominant Fe oxide in DDH03 borehole with minor limonite, jarosite, and goethite created thickness about 150–270 m in supergene zone; finally, this finding show a possibility of an extensive mineralization.  相似文献   

14.
The Miocene Qulong porphyry Cu‐Mo deposit, which is located at the Gangdese orogenic belt of Southern Tibet, is the largest porphyry‐type deposit in China, with confirmed Cu ～10 Mt and Mo ～0.5 Mt. It is spatially and temporally associated with multiphase granitic intrusions, which is accompanied by large‐scale hydrothermal alteration and mineralization zones, including abundant hydrothermal anhydrite. In addition to hydrothermal anhydrite, magmatic anhydrite is present as inclusions in plagioclase, interstitial minerals between plagioclase and quartz, and phenocrysts in unaltered granodiorite porphyry, usually in association with clusters of sulfur‐rich apatite in the Qulong deposit. These observations indicate that the Qulong magma‐hydrothermal system was highly oxidized and sulfur‐rich. Three main types of fluid inclusions are observed in the quartz phenocrysts and veins in the porphyry: (i) liquid‐rich; (ii) polyphase high‐salinity; and (iii) vapor‐rich inclusions. Homogenization temperatures and salinities of all type inclusions decrease from the quartz phenocrysts in the porphyry to hydrothermal veins (A, B, D veins). Microthermometric study suggests copper‐bearing sulfides precipitated at about 320–400°C in A and B veins. Fluid boiling is assumed for the early stage of mineralization, and these fluids may have been trapped at about 35–60 Mpa at 460–510°C and 28–42 Mpa at 400–450°C, corresponding to trapping depths of 1.4–2.4 km and 1.1–1.7 km, respectively.  相似文献   

15.
Copper–gold mineralization at the world‐class Batu Hijau porphyry deposit, Sumbawa Island, Indonesia, is closely related to the emplacement of multiple stages of tonalite porphyries. Petrographic examination indicates that at least two texturally distinct types of tonalite porphyries are currently recognized in the deposit, which are designated as “intermediate tonalite” and “young tonalite”. They are mineralogically identical, consisting of phenocrysts of plagioclase, hornblende, quartz, biotite and magnetite ± ilmenite, which are set in a medium‐coarse grained groundmass of plagioclase and quartz. The chemical composition of the rock‐forming minerals, including plagioclase, hornblende, biotite, magnetite and ilmenite in the tonalite porphyries was systematically analyzed by electron microprobe. The chemical data of these minerals were used to constrain the crystallization conditions and fluorine–chlorine fugacity of the corresponding tonalitic magma during its emplacement and crystallization. The crystallization conditions, including temperature (T), pressure (P) and oxygen fugacity (fO2), were calculated by applying the hornblende–plagioclase and magnetite–ilmenite thermometers and the Al‐in‐hornblende barometer. The thermobarometric data indicate that the tonalite porphyries were emplaced at 764 ± 22°C and 1.5 ± 0.3 × 105 kPa. If the pressure is assumed to be lithostatic, it is interpreted that the rim of hornblende and plagioclase phenocrysts crystallized at depths of approximately 5.5 km. As estimated from magnetite–ilmenite thermometry, the subsolidus conditions of the tonalite intrusion occurred at temperatures of 540–590°C and log fO2 ranging from ?20 to ?15 (between Ni‐NiO and hematite–magnetite buffers). This occurred at relatively high fO2 (oxidizing) condition. The fluorine–chlorine fugacity in the magma during crystallization was determined on the basis of the chemical composition of magmatic biotite. The calculation indicates that the fluorine–chlorine fugacity, represented by log (fH2O)/(fHF) and (fH2O)/(fHCl) in the corresponding tonalitic magma range from 4.31 to 4.63 and 3.62 to 3.79, respectively. The chlorine fugacity (HCl) to water (H2O) is relatively higher than the fluorine fugacity (HF to water), reflecting a high activity of chlorine in the tonalitic magma during crystallization. The relatively higher activity of chlorine (rather than fluorine) may indicate the significant role of chloride complexes (CuCl2? and AuCl2?) in transporting and precipitating copper and gold at the Batu Hijau deposit.  相似文献   

16.
Hydrogen‐ and oxygen‐isotope analyses of biotite (19), sericite (8), chlorite (2), quartz (27), and total rocks (37) from the Panguna porphyry‐copper deposit on Bougainville Island, place important constraints on the origin of the hydrothermal fluids responsible for mineralization and alteration in the mine region. Early high‐temperature amphibole‐magnetite alteration resulted from magmatic‐hydrothermal fluids. Several lines of evidence indicate 500°C as a realistic average temperature for mineralization, development of quartz veins, and biotitization processes. On the basis of mineral isotope data, responsible fluids could represent either 18O‐shifted ground‐waters or magmatic‐hydrothermal fluids at submagmatic temperatures. Independent evidence, as well as total‐rock 18O data, support the magmatic‐hydrothermal model.

Late‐stage sericitization processes probably resulted from fluids produced by 18O shifting of groundwaters during the evolution of the propylitic zone. Outermost quartz veins and biotitization conceivably resulted from fluids similar to those that caused sericitization, indicating that some interaction between relatively cool, 18O‐poor meteoric waters and the ore fluids occurred near the margins of the deposit. The origin of the chlorite‐sericite alteration cannot be resolved solely by isotope studies.  相似文献   

17.
Abstract: Ore specimens collected by the late Professor Takeo Watanabe from the Hol Kol and the Tul Mi Chung deposits, Suan mining district, Korean peninsula, were examined. In addition, measurements of sulfur isotopic ratio of ores and preliminary fluid inclusion microthermometry were carried out. Ores from the New orebody of the Hol Kol deposit consist mainly of bornite, wittichenite and chalcopyrite presently, which exhibit lamellae intergrowth texture, associated with native bismuth and electrum. Bismuthian bornite solid solution is considered to be a principal initial phases, while native bismuth was nucleated as molten bismuth melt initially. The occurrence of cubanite, miharaite, carrollite, siegenite, hessite and geikielite are recognized from the New orebody. Ores from the Eastern orebody of the Hol Kol deposit consist chiefly of chalcopyrite, occasionally associated with trace amounts of pyrrhotite, pyrite, bismuthinite and rare tellurobismuthite, while an ore specimen from the Western orebody consists mainly of sphalerite associated with chalcopyrite, pyrite and galena. Ores from the Tul Mi Chung deposit consist mainly of chalcopyrite and pyrite, occasionally associated with magnetite, sphalerite, galena and rare molybdenite. Some portions of magnetite are revealed to be silician magnetite. Sulfur fugacity is supposed to be below the stability field of bismuthinite in the New orebody. A reducing condition is suggested by the occurrence of geikielite without Fe3+ content. The sulfur and oxygen fugacities for the Eastern and Western orebodies of the Hol Kol deposit and for the Tul Mi Chung deposit were higher than the New orebody of the Hol Kol deposit. On the other hand, the Suan granite (porphyritic granodiorite) and the Chil Sing Dai granite (biotite granite porphyry) from the Hol Kol area can be classified as weakly magnetic magnetite‐series. Polyphase fluid inclusions are observed in gangue diopside associated with Cu ore of two specimens. The dissolution temperatures of daughter crystals are 394±26°C and 442±45°C, while the disappearing temperatures of vapor bubble were 475±25°C and > 500°C. Highly saline fluids were responsible for the mineralization at the Hol Kol deposit. The δ34S values of ore sulfides of the Hol Kol and the Tul Mi Chung deposit range from +11. 5% to +16. 1%, having anomalous lower values mainly from the Tul Mi Chung deposit. Such anomalous lower 634S values can be caused by isotopic fractionation against oxidized sulfur species. The δ34S value of bulk sulfur in the ore solutions responsible for the Hol Kol and the Tul Mi Chung deposit is estimated to be +13.5±2.5‰.  相似文献   

18.
Abstract. Determinations of SO3 and Cl contents of igneous accessory apatite were carried out on Late Cenozoic intermediate to silicic intrusive and volcanic rocks in the Japanese island arcs of the western Pacific rim including the southwestern Kuril arc (eastern Hokkaido), Northeast Japan arc (southwestern Hokkaido through northeastern Honshu to central Honshu), Izu‐Bonin arc, Kyushu‐Palau ridge, Southwest Japan arc (northern Kyushu) and northern Ryukyu arc (southern Kyushu). These were compared to those from the Western Luzon arc, Philippines, to better understand the metallogenesis of porphyry Cu deposits in the western Pacific island arcs. In addition, SO3 and Cl contents of accessory apatite in the Cretaceous magnetite‐series granitic rocks in the Kitakami belt (northeastern Honshu) and the Miocene ilmenite‐series granitic rocks in the Outer Zone of Southwest Japan (southern Kyushu) were also examined. Microphenocrystic apatites in shallow intrusions associated with porphyry Cu deposits in the Western Luzon arc contain >0.1 wt% S as SO3. Such high SO3 contents of microphenocrystic apatite are a common characteristic of hydrous mag‐matism in the Western Luzon arc, from 15 Ma old tonalitic plutonic rocks of the Luzon Central Cordillera to present‐day volcanism at Mount Pinatubo. The accessory apatite in intrusive rocks associated with porphyry Cu deposits, especially those at the Santo Tomas II deposit, show significantly high Cl contents (>2 wt%). The SO3 contents of microphenocrystic apatite in most of the hydrous silicic rocks along the volcanic front, in andesites related to native sulfur deposits, and in Miocene and younger shallow granitic intrusions in northeastern Honshu, are generally <0.1 wt%. On the other hand, the SO3 contents of apatite in such rocks from eastern Hokkaido, southwestern Hokkaido, Izu, northern Kyushu and southern Kyushu are similar to those from the Western Luzon arc. The SO3 contents of accessory apatite in the Cretaceous magnetite‐series granitic rocks in the Kitakami belt are variable, whereas those of the Miocene ilmenite‐series granitic rocks in southern Kyushu are extremely low. The Cl contents of accessory apatite in some rocks of the Northeast Japan arc, Izu‐Bonin arc and Southwest Japan arc are significantly high. In terms of the Cl and SO3 contents of microphenocrystic apatite, Cenozoic Japanese arc magmatism show similarities with arc magmatism associated elsewhere with porphyry Cu mineralization, except for the most of northeastern Honshu of the Northeast Japan arc. Apatite commonly occurs as inclusions in other phenocrystic phases. Thus the variation in SO3 contents of apatite is a feature of early stage magmatic differentiation. The SO3 contents of microphenocrystic apatite are considered to reflect the redox state of the magma source region or fluids encountered during magma generation.  相似文献   

19.
Akira Imai    Yuki Nagai 《Resource Geology》2009,59(3):231-243
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.  相似文献   

20.
中国还原性斑岩矿床研究进展及判别标志   总被引：1，自引：1，他引：0  
申萍  潘鸿迪 《岩石学报》2020,36(4):967-994
世界上大多数斑岩矿床的成矿流体为氧化流体(CO_2 CH_4)。然而,Rowins(2000)提出一些斑岩Cu-Au矿床的成矿流体为富含CH_4的还原流体,矿床缺乏磁铁矿、赤铁矿和硬石膏等表征高氧逸度的矿物,而发育大量的磁黄铁矿,矿床规模小,矿床形成与含钛铁矿的还原性的Ⅰ型花岗岩类有关,并将其称之为还原性斑岩Cu-Au矿床。我国学者研究发现,中国不但发育还原性斑岩铜矿床,还发育还原性斑岩-矽卡岩铜矿床和还原性斑岩钼矿床,我们建议将这三种矿床统称为还原性斑岩矿床。本文基于课题组近十年来的研究工作,并结合前人的研究成果,综合分析了中国发育的大中型还原性斑岩矿床的典型实例,在此基础上,重点阐明中国大型还原性斑岩矿床的特点、流体中CH_4来源及其有关的成矿作用、容矿围岩特点、成矿岩浆氧化还原状态及其成因、矿床形成的构造背景等。与Rowins(2000)提出的还原性斑岩铜矿床规模小的特点不同,中国发育的一些还原性斑岩矿床规模大;我们研究还识别出该类矿床发育独特的热液矿物和矿石矿物,比如,还原性斑岩铜矿发育热液钛铁矿,矿石矿物以黄铜矿为主,罕见斑铜矿、辉铜矿等矿物;还原性斑岩钼矿床出现热液钛铁矿,矿石矿物以辉钼矿为主,罕见黑钨矿和锡石等矿物;还原性斑岩-矽卡岩铜矿床的矽卡岩期发育钙铝榴石、钙铁辉石等还原性矽卡岩矿物和大量的磁黄铁矿,热液期以发育黄铜矿而非斑铜矿和辉铜矿等矿石矿物为特征。因此,还原性斑岩矿床除了Rowins(2000)提出的发育富CH_4还原流体和磁黄铁矿等识别标志之外,还可辅以独特的脉石矿物(如钛铁矿、钙铝榴石、钙铁辉石等)和简单的矿石矿物(如黄铜矿、辉钼矿等)这两个标志进行识别。中国还原性斑岩矿床含矿岩体的围岩中普遍发育还原性岩石(如含碳质沉积岩或火山沉积岩、含亚铁的火山岩或火山沉积岩等);对于成矿流体中CH_4、C_2H_6等还原性气体的来源,多数学者认为CH_4、C_2H_6等还原性气体主要源于还原性围岩,部分源于岩浆。关于还原性斑岩矿床的成矿岩体是否为含钛铁矿的、还原性的花岗岩类,目前研究较少且存在争议,多数学者认为成矿原始岩浆为氧化性岩浆,但其氧逸度偏低,少数学者认为成矿岩浆始终为还原岩浆。还原性斑岩矿床与经典的斑岩矿床的成矿构造背景类似,二者没有明显区别。还原性斑岩矿床显示的还原性热液蚀变和成矿特点均与成矿流体富含CH_4还原气体密切相关,因此,富含CH_4还原流体是还原性斑岩矿床形成的关键。  相似文献   

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