Geology,alteration, age,and origin of iron oxide–apatite deposits in Upper Eocene quartz monzonite,Zanjan district,NW Iran

Iron oxide–apatite deposits are present in Upper Eocene pyroxene-quartz monzonitic rocks of the Zanjan district, northwestern Iran. Mineralization occurred in five stages: (1) deposition of disseminated magnetite and apatite in the host rock; (2) mineralization of massive and banded magnetite ores in veins and stockwork associated with minor brecciation and calcic alteration of host rocks; (3) deposition of sulfide ores together with potassic alteration; (4) formation of quartz and carbonate veins and sericite, chlorite, epidote, silica, carbonate, and tourmaline alteration; and (5) supergene alteration and weathering. U–Pb dating of monazite inclusions in the apatite indicates an age of 39.99?±?0.24 Ma, which is nearly coeval with the time of emplacement of the host quartz monzonite, supporting the genetic connection. Fluid inclusions in the apatite have homogenization temperatures of about 300 °C and oxygen isotopic compositions of the magnetite support precipitation from magmatic fluids. Late-stage quartz resulted from the introduction of a cooler, less saline, and isotopically depleted fluid. The iron oxide–apatite deposits in the Tarom area of the Zanjan district are typical of a magmatic–hydrothermal origin and are similar to the Kiruna-type deposits with respect to mineral assemblages, fabric and structure of the iron ores, occurrence of the ore bodies, and wall rock alteration.     

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.     

Geochemistry and Genesis of Iron-apatite Ore in the Khanlogh Deposit, Eastern Cenozoic Quchan-Sabzevar Magmatic Arc, NE Iran

The Khanlogh deposit in the Cenozoic Quchan-Sabzevar magmatic belt, NE Iran, is hosted by Oligocene granodioritic rock. The Khanlogh intrusive body is I-type granitoid of the calc-alkaline series. The orebodies are vein, veinlet, massive, and breccia in shape and occur along the fault zones and fractures within the host rock. Ore minerals dominantly comprise magnetite and apatite associated with epidote, clinopyroxene, calcite, quartz, and chlorite. Apatites of the Khanlogh deposit have a high concentration of REE, and show a strong LREE/HREE ratio with a pronounced negative Eu anomaly. Magnetites have a high concentration of REE and show weak to moderate LREE/HREE fractionation. They are comparable to the REE patterns in Kiruna-type iron ores and show an affinity to calc-alkaline magmas. The Khanlogh deposit is similar in the aspects of host rock lithology, alteration, mineralogy, and mineral chemistry to the Kiruna-type deposits. Field observations, hydrothermal alteration halos, style of mineralization, and the geochemical characteristics of apatite, magnetite, and host rock indicate that these magnetite veins have hydrothermal origin similar to Cenozoic Kiruna-type deposits within the Tarom subzone, NW Iran, and are not related to silica-iron oxide immiscibility, as are the major Precambrian magnetite deposits in central Iran.     

Geochronology and Ore‐Forming Fluids of the Baizhangyan W–Mo Deposit in the Chizhou Area,Middle‐Lower Yangtze Valley,SE‐China

The Baizhangyan skarn‐porphyry type W–Mo deposit is located in a newly defined Mo–W–Pb–Zn metallogenic belt, which is in the south of Middle‐Lower Yangtze Valley Cu–Fe–Au polymetallic metallogenic belt in SE China. The W–Mo orebodies occur mainly within the contact zone between fine‐grained granite and Sinian limestone strata. There are two types of W–Mo mineralization: major skarn W–Mo mineralization and minor granite‐hosted disseminated Mo mineralization which was traced by drilling at depth. Eight molybdenite samples from Mo‐bearing ores yield Re–Os dates that overlap within analytical error, with a weighted average age of 134.1 ± 2.2 Ma. These dates are in close agreement with SIMS U–Pb concordant zircon age for fine‐grained granite at 133.3 ± 1.3 Ma, indicating that crystallization of the granite and hydrothermal molybdenite formation were coeval and likely cogenetic. The Baizhangyan W–Mo deposit formed in the Early Cretaceous extensional tectonic setting at the Middle‐Lower Yangtze Valley metallogenic belt and the Jaingnan Ancient Continent. Based on mineral compositions and crosscutting relationships of veinlets, hydrothermal alteration and mineralization, the ore mineral paragenesis of the Baizhangyan deposit is divided into four stages: skarn stage (I), oxide stage (II), sulfide stage (III), and carbonate stage (IV). Fluid inclusions in garnet, scheelite, quartz and calcite from W–Mo ores are mainly aqueous‐rich (L + V) type inclusions. Following garnet deposition at stage I, the high‐temperature fluids gave way to progressively cooler, more dilute fluids associated with tungsten–molybdenite–base metal sulfide deposition (stage II and stage III) (162–360°C, 2.7–13.2 wt % NaCl equivalent) and carbonate deposition (stage IV) (137–190°C, 0.9–5 wt % NaCl equiv.). Hydrogen‐oxygen isotope data from minerals of different stages suggest that the ore‐forming fluids consisted of magmatic water, mixed in various proportions with meteoric water. From stage I to stage IV, there is a systematic decrease in the homogenization temperature of the fluid‐inclusion fluids and calculated δ¹⁸O values of the fluids. These suggest that increasing involvement of formation water or meteoric water during the fluid ascent resulted in successive deposition of scheelite and molybdenite at Baizhangyan.     

Implication of Apatite and Anhydrite for Formation of an Iron‐Oxide‐Apatite (IOA) Rare Earth Element Prospect,Benjamin River,Canada

The Benjamin River apatite prospect in northern New Brunswick, Canada, is hosted by the Late Silurian Dickie Brook plutonic complex, which is made up of intrusive units represented by monzogranite, diorite and gabbro. The IOA ores, composed mainly of apatite, augite, and magnetite at Benjamin River form pegmatitic pods and lenses in the host igneous rocks, the largest of which is 100 m long and 10–20 m wide in the diorite and gabbro units. In this study, 28 IOA ore and rock samples were collected from the diorite and gabbro units. Mineralogical observations show that the apatite–augite–magnetite ores are variable in the amounts of apatite, augite, and magnetite and are associated with minor amounts of epidote‐group minerals (allanite, REE‐rich epidote and epidte) and trace amounts of albite, titanite, ilmenite, titanomagnetite, pyrite, chlorite, calcite, and quartz. Apatite and augite grains contain small anhydrite inclusions. This suggests that the magma that crystallized apatite and augite had high oxygen fugacity. In back scattered electron (BSE) images, apatite grains in the ores have two zones of different appearance: (i) primary REE‐rich zone; and (ii) porous REE‐poor zone. The porous REE‐poor zones mainly appear in rims and/or inside of the apatite grains, in addition to the presence of apatite grains which totally consist of a porous REE‐poor apatite. This porous REE‐poor apatite is characterized by low REE (<0.84 wt%), Si (<0.28 wt%), and Cl (<0.17 wt%) contents. Epidote‐group minerals mainly occur in grain boundary between the porous REE‐poor apatite and augite. These indicate that REE leached from primary REE‐rich apatite crystallized as allanite and REE‐rich epidote. Magnetite in the ores often occurs as veinlets that cut apatite grains or as anhedral grains that replace a part of augite. These textures suggest that magnetite crystallized in the late stage. Pyrite veins occur in the ores, including a large amount of quartz and calcite veins. Pyrite veins mainly occur with quartz veins in augite. These textures indicate pyrite veins are the latest phase. Apatite–augite–magnetite ore, gabbro–quartz diorite and feldspar dike collected from the Benjamin River prospect contain dirty pure albite (Ab₉₈Or₂–Ab₁₀₀) under the microscope. The feldspar dikes mainly consist of dirty pure albite. Occurrences of the dirty pure albite suggest remarkable albitization (sodic alteration) of original plagioclase (An_25.3–An₆₀ in Pilote et al., 2012) associating with intrusion of monzogranite into gabbro and diorite. SO₄^2? bearing magma crystallized primary REE‐rich apatite, augite and anhydrite reacted with Fe in the sodic fluids, which result in oxidation of Fe²⁺ and release of S^2? into the sodic fluids. REE, Ca and Fe from primary REE‐rich apatite, augite and plagioclase altered by the sodic fluids were released into the fluids. Then Fe³⁺ in the sodic fluids precipitated as Fe oxides and epidote‐group minerals in apatite–augite–magnetite ores. Finally, residual S^2? in sodic fluids crystallized as latest pyrite veins. In conclusion, mineralization in Benjamin River IOA prospect are divided into four stages: (1) oxidized magmatic stage that crystallized apatite, augite and anhydrite; (2) sodic metasomatic stage accompanying alteration of magmatic minerals; (3) oxidized fluid stage (magnetite–epidote group minerals mineralization); and (4) reduced fluid stage (pyrite mineralization).     

Hydrothermal alteration and K–Ar ages of Neogene‐Quaternary magmatic‐hydrothermal systems at Toyoha‐Muine area in southwest Hokkaido,Japan

This paper presents a review of hydrothermal alteration and K–Ar age data from the Toyoha‐Muine area (TMA), where the Toyoha polymetallic (Ag–Pb–Zn–Cu–In) deposit is located near the Pliocene andesitic volcano that formed Mt Muine. Systematic prospect‐scale mapping, sampling, X‐ray analysis and microscopic observation show that hydrothermal alteration is divided into two groups: acid‐pH and neutral‐pH alteration types. The former is further divided into mineral assemblages I, II and III, while the latter into mineral assemblages IV and V. Different mineralogical features in five mineral assemblages are summarized as follows: (I) Quartz (silicified rock); (II) Pyrophyllite or dickite; (III) Kaolinite or halloysite ± alunite; (IV) Sericite or K‐feldspar; and (V) Interstratified minerals (illite/smectite and chlorite/smectite) and/or smectite. K–Ar radiometric ages determined on twenty‐eight K‐bearing samples (whole volcanic rocks and separated hydrothermal minerals) mainly fall into one of three periods: Early Miocene (24.6–21.4 Ma), Middle–Late Miocene (12.5–8.4 Ma) and Pliocene–Pleistocene (3.2–0 Ma). These three periods are characterized as follows. Early Miocene: A minor hydrothermal activity, which might be genetically related to the intermediate or felsic magmatic activities, formed mineral assemblage IV at 24.6 Ma in the northern part of the TMA. Middle to Late Miocene: The basaltic intrusion, andesitic eruption, and granodiorite intrusions induced hydrothermal activities between 12.5 and 8.4 Ma, resulting in the formation of a mineral assemblage IV with some base metal mineralization. Pliocene–Pleistocene: An andesitic eruption formed Mt Muine between 3.2 and 2.9 Ma. The andesitic activity was associated with acid‐pH mineral assemblages I, II and III locally around the volcano. Latent magmatic intrusions subsequent to the andesitic eruption generated hydrothermal activities that formed mineral assemblages IV and V between 1.9 and 0 Ma in the southern and southeastern parts of Toyoha deposit at depth, overprinting the Middle to Late Miocene alteration. The hydrothermal activities also formed mineral assemblages I, II and III along the Yunosawa fault (east of the Toyoha deposit) and assemblage III in the south and southeast of the Toyoha deposit near the surface.     

富碱侵入岩与金成矿关系：云南省姚安金矿床 成矿流体形成演化的微量元素和同位素证据

以产在姚安富碱侵入岩体内外接触带上的姚安金矿床为对象，对成矿流体形成演化过程中的微量元素和S、C同位素地球化学进行了综合研究。研究结果表明，富碱侵入岩成岩过程中分异出的岩浆流体提供了姚安金矿床早期成矿作用所必需的成矿流体；从早期成矿阶段至晚期成矿,民矿流体经历了从以岩浆流体为主的流体体系至以大气降水为主的流体体系的转变。因此，钙碱性侵入岩成岩过程中可分异出成矿流体的过程，也存在于富碱浸入岩的成岩过程中。     

Geology and Re-Os Geochronology of Mineralization of the Miduk Porphyry Copper Deposit, Iran

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.     

Cenozoic magmatism in Kalimantan and its related geodynamic evolution

The NE–SW Tertiary magmatic belt of central Kalimantan is related to two separate periods of subduction; during the Eocene–Oligocene and Late Oligocene–Miocene. The younger magmatic belt is superimposed upon the earlier belt. This magmatic belt is characterized chiefly by Late Oligocene–Miocene volcanic products, among which limited exposures of the Eocene volcanics have also been mapped by previous investigators. This calc-alkaline magmatic belt has become known as the ‘gold belt’ of Central West Kalimantan on account of a number of discoveries of Neogene epithermal gold mineralization. This mineralization is found in central to proximal volcanic settings and occurred at relatively shallow depths. The earliest known subduction-related magmatism took place in the Eocene–Early Oligocene with the emplacement of calc-alkaline silicic pyroclastics, followed by a period of continental collision. Subsequent subduction-related magmatism continued from Late Oligocene–Pleistocene, during which time the magma evolved from calc-alkaline to potassic calc-alkaline. Plio-Pleistocene magmatism resulted in the formation of basalt flows. The present available K–Ar ages of the Cenozoic volcanics range from 51 to 1 Ma.     

Geology and Geochemistry of the Bianbianshan Au‐Ag‐Cu‐Pb‐Zn Deposit,Southern Da Hinggan Mountains,Northeastern China

The Bianbianshan deposit, the unique gold-polymetal (Au-Ag-Cu-Pb-Zn) veined deposit of the polymetal metallogenic belt of the southern segment of Da Hinggan Mountains mineral province, is located at the southern part of the Hercynian fold belt of the south segment of Da Hinggan Mountains mineral province, NE China. Ores at the Bianbianshan deposit occur within Cretaceous andesite and rhyolite in the form of gold-bearing quartz veins and veinlet groups containing native gold, electrum, pyrite, chalcopyrite, galena and sphalerite. The deposit is hosted by structurally controlled faults associated with intense hydrothermal alteration. The typical alteration assemblage is sericite + chlorite + calcite + quartz, with an inner pyrite - sericite - quartz zone and an outer seicite - chlorite - calcite - epidote zone between orebodies and wall rocks. δ34 S values of 17 sulfides from ores changing from –1.67 to +0.49‰ with average of –0.49‰, are similar to δ34 S values of magmatic or igneous sulfide sulfur. 206Pb/204Pb, 207Pb/204Pb and 208Pb/ 204Pb data of sulfide from ores range within 17.66–17.75, 15.50–15.60, and 37.64–38.00, respectively. These sulfur and lead isotope compositions imply that ore-forming materials might mainly originate from deep sources. H and O isotope study of quartz from ore-bearing veins indicate a mixed source of deep-seated magmatic water and shallower meteoric water. The ore formations resulted from a combination of hydrothermal fluid mixing and a structural setting favoring gold-polymetal deposition. Fluid mixing was possibly the key factor resulting in Au-Ag-Cu-Pb-Zn deposition in the deposit. The metallogenesis of the Bianbianshan deposit may have a relationship with the Cretaceous volcanic-subvolcanic magmatic activity, and formed during the late stage of the crust thinning of North China.     

Magmatic‐Hydrothermal Mineralization Sequence in Xinlu Ore Field,Guangxi, South China: Constraints from Zircon U‐Pb,Molybdenite Re‐Os,and Muscovite Ar‐Ar Dating

The Xinlu Sn‐polymetallic ore field is located in the western Nanling Polymetallic Belt in northeastern Guangxi, South China, where a number of typical skarn‐, hydrothermal vein‐type tin deposits have developed. There are two types of Sn deposits: skarn‐type and sulfide‐quartz vein‐type. The tin mineralizations mainly occur on the south side of the Guposhan granitic complex pluton and within its outer contact zone. To constrain the Sn mineralization age and further understand its genetic links to the Guposhan granitic complex, a series of geochronological works has been conducted at the Liuheao deposit of the ore field using high‐precision zircon SHRIMP U‐Pb, molybdenite Re‐Os, and muscovite Ar‐Ar dating methods. The results show that the biotite‐monzogranite, which is part of the Xinlu intrusive unit of the Guposhan complex pluton, has a SHRIMP U‐Pb zircon age of 161.0 ± 1.5 Ma. The skarn‐type ore has a ⁴⁰Ar‐³⁹Ar muscovite plateau age of 160 ± 2 Ma (same as its isochron age), and the sulfide‐quartz vein‐type ore yields an Re‐Os molybdenite isochron age of 154.4 ± 3.5 Ma. The magmatic‐hydrothermal geochronological sequence demonstrated that the hydrothermal mineralization took place immediately following the emplacement of the monzogranite, with the skarn metasomatic mineralization stage predating the sulfide mineralization stage. Geochronologically, we have compared this ore field with 26 typical Sn deposits distributed along the Nanling Polymetallic Belt, leading to the suggestion of the magmatic‐metallogenic processes in the Xinlu ore field (ca. 161–154 Ma) as a component of the Early Yanshanian large‐scale Sn‐polymetallic mineralization event (peaked at 160–150 Ma) in the Nanling Range of South China. Petrogenesis of Sn‐producing granite and Sn‐polymetallic mineralization were probably caused by crust–mantle interaction as a result of significant lithospheric extension and thinning in South China in the Late Jurassic.     

Overprinting porphyry‐type veinlets on the intrusive rocks and phreatomagmatic breccias in the Southwest prospect,southwestern Sto. Tomas II (Philex), Baguio District,Philippines

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 X_Mg 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.     

安徽庐枞沙溪斑岩铜矿蚀变及矿化特征研究

沙溪斑岩铜矿是长江中下游成矿带中部庐枞火山岩盆地外围的一个大型铜矿床.本文在前人工作基础上,基于详细的野外观察和系统的岩相学、矿相学工作,详细研究了矿床的蚀变特征及分带.结果表明,矿床的蚀变类型有钾硅酸盐化、青磐岩化、长石分解蚀变和高岭土化,从深到浅依次发育有钾硅酸盐化、长石分解蚀变叠加钾硅酸盐化、长石分解蚀变和高岭土化等蚀变.确定了矿化特征、矿物生成顺序并划分了成矿阶段,即:钾硅酸盐阶段、石英硫化物阶段和石英碳酸盐阶段,其中,石英硫化物阶段又可进一步分为石英硫化物亚阶段和绿帘石-绿泥石亚阶段.基于蚀变及矿化特征认为,沙溪铜矿床的矿化始于钾硅酸盐阶段的晚期,石英硫化物亚阶段是黄铜矿主要的沉淀阶段,石英碳酸盐阶段也对成矿贡献了部分铜质.与世界上不同构造环境的典型斑岩铜矿床对比认为,沙溪矿床总体上与这些矿床的蚀变、矿化特征类似;与陆缘弧、岛弧、陆内碰撞造山后伸展环境矿床在矿体产出位置、蚀变分带方面相似;而由于围岩性质的差异,与板内环境的德兴矿床在矿体位置、蚀变分带方面存在差异,但是二者在脉体类型特别是与矿化关系密切的脉体特征上较为一致.因此,对于斑岩型矿床而言,构造背景可能控制了其岩浆的形成、演化以及含矿性,而岩浆岩最终定位的深度、围岩等条件则控制了其蚀变、矿化特征.     

Fluid Inclusions and Hydrogen,Oxygen, Sulfur Isotopes of Nuri Cu‐W‐Mo Deposit in the Southern Gangdese,Tibet

The Nuri Cu‐W‐Mo deposit is located in the southern subzone of the Cenozoic Gangdese Cu‐Mo metallogenic belt. The intrusive rocks exposed in the Nuri ore district consist of quartz diorite, granodiorite, monzogranite, granite porphyry, quartz diorite porphyrite and granodiorite porphyry, all of which intrude in the Cretaceous strata of the Bima Group. Owing to the intense metasomatism and hydrothermal alteration, carbonate rocks of the Bima Group form stratiform skarn and hornfels. The mineralization at the Nuri deposit is dominated by skarn, quartz vein and porphyry type. Ore minerals are chalcopyrite, pyrite, molybdenite, scheelite, bornite and tetrahedrite, etc. The oxidized orebodies contain malachite and covellite on the surface. The mineralization of the Nuri deposit is divided into skarn stage, retrograde stage, oxide stage, quartz‐polymetallic sulfide stage and quartz‐carbonate stage. Detailed petrographic observation on the fluid inclusions in garnet, scheelite and quartz from the different stages shows that there are four types of primary fluid inclusions: two‐phase aqueous inclusions, daughter mineral‐bearing multiphase inclusions, CO₂‐rich inclusions and single‐phase inclusions. The homogenization temperature of the fluid inclusions are 280°C–386°C (skarn stage), 200°C–340°C (oxide stage), 140°C–375°C (quartz‐polymetallic sulfide stage) and 160°C–280°C (quartz‐carbonate stage), showing a temperature decreasing trend from the skarn stage to the quartz‐carbonate stage. The salinity of the corresponding stages are 2.9%–49.7 wt% (NaCl) equiv., 2.1%–7.2 wt% (NaCl) equiv._, 2.6%–55.8 wt% (NaCl) equiv. and 1.2%–15.3 wt% (NaCl) equiv., respectively. The analyses of CO₂‐rich inclusions suggest that the ore‐forming pressures are 22.1 M Pa–50.4 M Pa, corresponding to the depth of 0.9 km–2.2 km. The Laser Raman spectrum of the inclusions shows the fluid compositions are dominated in H₂O, with some CO₂ and very little CH₄, N₂, etc. δD values of garnet are between ?114.4‰ and ?108.7‰ and δ¹⁸O_H2O between 5.9‰ and 6.7‰; δD of scheelite range from ?103.2‰ to ?101.29‰ and δ¹⁸O_H2O values between 2.17‰ and 4.09‰; δD of quartz between ?110.2‰ and ?92.5‰ and δ¹⁸O_H2O between ?3.5‰ and 4.3‰. The results indicate that the fluid came from a deep magmatic hydrothermal system, and the proportion of meteoric water increased during the migration of original fluid. The δ³⁴S values of sulfides, concentrated in a rage between ?0.32‰ to 2.5‰, show that the sulfur has a homogeneous source with characteristics of magmatic sulfur. The characters of fluid inclusions, combined with hydrogen‐oxygen and sulfur isotopes data, show that the ore‐forming fluids of the Nuri deposit formed by a relatively high temperature, high salinity fluid originated from magma, which mixed with low temperature, low salinity meteoric water during the evolution. The fluid flow through wall carbonate rocks resulted in the formation of layered skarn and generated CO₂ or other gases. During the reaction, the ore‐forming fluid boiled and produced fractures when the pressure exceeded the overburden pressure. Themeteoric water mixed with the ore‐forming fluid along the fractures. The boiling changed the pressure and temperature, oxygen fugacity, physical and chemical conditions of the whole mineralization system. The escape of CO₂ from the fluid by boiling resulted in scheelite precipitation. The fluid mixing and boiling reduced the solubility of metal sulfides and led the precipitation of chalcopyrite, molybdenite, pyrite and other sulfide.     

西藏驱龙巨型斑岩Cu Mo矿床的富S、高氧化性含矿岩浆——来自岩浆成因硬石膏的证据

西藏冈底斯成矿带上的驱龙巨型斑岩Cu-Mo矿床以发育大量的硬石膏为特征.详细的岩相学研究发现:驱龙矿床不仅发育热液脉状的硬石膏,含矿斑岩中还产出岩浆成因硬石膏,这在国内系首次报道.观察表明,在岩浆演化早期的花岗闪长岩、黑云母二长花岗岩中,岩浆硬石膏以矿物包体的形式产于斜长石、石英中;在主成矿期的二长花岗斑岩、花岗闪长斑岩中,岩浆硬石膏以矿物包体产于斜长石斑晶中,局部以斑晶形式产出,并伴有富S的磷灰石(SO_3含量为0.11%～0.44%)、磁铁矿发育.后期热液活动也形成了大量的硬石膏±石英+硫化物脉,是矿区主要的矿化类型之一.电子探针分析结果显示,后期的热液硬石膏与岩浆硬石膏相比,在微量成分上明显富集Sr(分别为0.24%和0.03%),可能是由于在岩浆-热液演化过程中,Sr的不相容性或者/以及粘土化蚀变造成的.岩浆硬石膏以及与之共生的富S磷灰石的出现,明确指示驱龙矿床成矿岩浆具有富S、高氧逸度的特征;同时也为研究S在斑岩型矿床岩浆演化过程中的状态、行为,提供了很好的研究对象.     

辽宁刘屯金矿床地质特征及成因

刘屯金矿床为含金硫化物石英脉型,矿体直接围岩为晚太古代混合花岗岩。区域上建平群大营子组为金的矿源层,金成矿与中生代构造岩浆活动密切相关。含金石英脉(矿脉)严格地受近东西向断裂构造控制。据硫同位素组成证明矿石、围岩、中生代侵入岩具有同一性,为幔源硫。氢氧同位素组成则显示了成矿溶液的多成因特征。矿石中铅同位素为古老的铅体系,与中生代岩体的长石铅属同一源地。通过时矿床成因的探讨,认为是"岩浆热源-混合热液"型复成因金矿床,成矿时代为燕山期。     

山东大张矽卡岩型铁矿床中铁的富集机制 ——来自流体包裹体和氢、氧同位素的证据

大张铁矿是鲁西地区近年来新发现的一个重要的矽卡岩型矿床.矿体主要赋存于石英二长闪长岩与奥陶系马家沟组灰岩接触带及其附近.根据脉体穿插关系和交代蚀变特征,将大张矽卡岩型铁矿床成矿过程划分为矽卡岩阶段、氧化物阶段、硫化物阶段和碳酸盐阶段.通过对透辉石、绿帘石、石英和方解石等透明矿物显微观察发现,大张铁矿中流体包裹体类型主要...     

Highly Oxidized Magma and Fluid Evolution of Miocene Qulong Giant Porphyry Cu‐Mo Deposit,Southern Tibet,China

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.     

庐枞盆地大倪庄铜矿床地质特征、成岩时代及成因探讨

大倪庄铜矿是庐枞盆地内部近年来发现的一处小型斑岩型矿床。本次工作以大倪庄铜矿为研究对象,基于详细的野外观察和系统的岩相学、矿相学工作,总结了矿床的蚀变特征,即主要发育:钾硅酸盐化、黄铁绢英岩化、青磐岩化、碳酸盐化蚀变;确定了矿化特征、矿物生成顺序并划分了成矿阶段,即:钾硅酸盐化阶段、硫化物阶段、碳酸盐化阶段,其中硫化物阶段可进一步划分为石英硫化物亚阶段、绿帘石-绿泥石亚阶段。通过对与成矿有关的侵入岩体(正长斑岩)采用LA-ICP-MS锆石U-Pb定年,获得正长斑岩LA-ICP-MS锆石U-Pb年龄为(126.6±1.8)Ma,形成时代为早白垩世,对应于盆地内双庙旋回岩浆侵入活动。通过与其他区域相似矿床对比分析,探究了此类矿床控矿因素,为该地区斑岩型铜矿找矿勘查提供参考。     

The Crater Mountain Deposit,Papua New Guinea: Porphyry‐related Au–Te System

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.