鄂东南铜山口铜(钼)矿床黑云母矿物化学特征及其对岩石成因与成矿的指示

在鄂东南铜山口铜(钼)矿床存在着3种产状的黑云母,分别是赋存于花岗闪长斑岩矿物颗粒间的黑云母、钾长石斑晶内的黑云母以及蚀变带内的黑云母。本文运用电子探针(EMPA)和激光剥蚀-等离子体质谱(LA-ICP-MS)技术,对这3种不同产状的黑云母进行了原位成分分析。结果表明,3种产状的黑云母Ti的含量介于0.38～0.45之间,且Mg/(Mg+Fe)介于0.53～0.72之间,类似于岩浆成因黑云母的成分特征。3种产状的黑云母MgO和FeOT值差别较大,但Al2O3、TiO2、SiO2、Na2O和K2O值差别不明显。作为花岗闪长斑岩质熔体中Rb、Ba、Nb、Ta等不相容元素及Sc、V、Co、Ni、Cr等相容元素的主要载体,黑云母的U、Th、Pb、Sr、Zr、Hf、Y等元素含量显著低于主岩,而且高场强元素Nb、Ta受后期岩浆热液作用的影响较弱。黑云母并不是影响全岩稀土特征的主要矿物相。铜山口花岗闪长斑岩的形成与幔源岩浆作用关系密切,并可能与板块俯冲作用相关。黑云母含Cu量的高低并不是衡量侵入体是否成矿的有效指标,但体系中高的氧逸度(logfO2NiNiO+1),有利于斑岩铜矿的形成。与Cu成矿有关的黑云母具有高镁低铁的特征,与Sn成矿有关的黑云母则具有高铁低镁的特征。     

Minor element- and carbonaceous material thermometry of high-grade metapelites from the Sauwald Zone, Southern Bohemian Massif (Upper Austria)

The Sauwald area is located at the southern rim of the Bohemian Massif and contains migmatites and high-grade metapelitic and granitic gneisses. These rocks were metamorphosed during the post-collisional high-T/low-P stage of the Variscan metamorphic event (~330 Ma). Metapelitic samples were taken from two localities near Kössldorf and Pyret in Upper Austria and the investigated samples contain the mineral assemblage garnet + cordierite + spinel + sillimanite + K-feldspar + quartz + biotite + muscovite + magnetite + graphite. An important aspect of this study is the evaluation of previously published P-T estimates for these high-grade metapelites (Knop et al. 1995; Tropper et al. 2006) involving Ti-in-biotite, Na-in-cordierite thermometry and the micro-Raman thermometer based upon the degree of crystallization of carbonaceous material. In the two samples studied three texturally and chemically different biotites are distinguished. Biotite inclusions in garnet have the highest Ti contents of 5–6 wt.% TiO₂. Matrix biotites contain 2–4 wt.% TiO₂ and biotites from late-stage muscovite-biotite symplectites contain <2 wt.% TiO₂. This corresponds to temperatures of 730–760°C (stage 1), 600–700°C (stage 2), and 550–610°C (stage 3). Since the Ti-in-biotite thermometer strongly depends on X _Mg of biotite, which is susceptible to changes during retrogression the calculated temperatures for stage 1 are interpreted as minimum temperatures of the peak metamorphic stage. The Na contents of the studied cordierites vary from 0.1 to 0.2 wt.% Na₂O. Application of the Na-in-cordierite thermometer yields temperatures in the range of 770–900°C; they are strongly dependent on the bulk Na₂O content of the samples. The micro-Raman geothermometer of graphite was applied to carbonaceous material, which occurs as inclusions in garnet and cordierite. It yielded a maximum temperature >650°C, i.e. above the calibration limit of this method. This study shows that the obtained temperature estimates agree well with the P-T estimates based on phase equilibrium thermobarometry (Knop et al. 1995; Tropper et al. 2006), thus illustrating the validity of these thermometers. Nevertheless in order to more precisely constrain the metamorphic evolution of these high-grade rocks, better constrained experimental calibrations of, for instance the Na-in-cordierite thermometer, are clearly needed.     

A Report on a Biotite-Calcic Hornblende Geothermometer

This paper presents a biotite-calcic hornblende geothermometer which was empirically calibrated based on the gamet-biotite geothermometer and the gamet-plagioclase-hornblende-quartz geobarometer, in the ranges of 560-800℃ (T) and 0.26-1.4 GPa (P) using the data of metadolerite, amphibolite, metagabbro, and metapelite collected from the literature. Biotite was treated as symmetric Fe-Mg-AlVI-Ti quaternary solid solution, and calcic hornblende was simplified as symmetric Fe-Mg binary solid solution. The resulting thermometer may rebuild the input garnet-biotite temperatures well within an uncertainty of ±50℃. Errors of ±0.2 GPa for input pressure, along with analytical errors of ?% for the relevant mineral compositions, may lead to a random error of ±16℃ for this thermometer, so that the thermometer is almost independent of pressure estimates. The thermometer may clearly discriminate different rocks of lower amphibolite, upper amphibolite and granulite facies on a high confidence level. It is assume     

Calibration of the garnet–biotite–Al2SiO5–quartz geobarometer for metapelites

A garnet–biotite–Al₂SiO₅–quartz (GBAQ) geobarometer was empirically calibrated using more than 700 natural metapelites with a broad compositional range of garnet and biotite under P–T conditions of 450–950°C and 1–17 kbar. In the calibration, activity models of garnet and biotite identical to those in the garnet–biotite (GB) geothermometer of Holdaway [American Mineralogist 2000, 85: 881–892] were used. Therefore, the GBAQ geobarometer and the GB geothermometer can be simultaneously applied to iteratively estimate metamorphic P–T conditions. Successful applications of the GBAQ geobarometer to natural metapelites certify its validity. Most importantly, when plagioclase is absent or CaO components in garnet and/or plagioclase are deficient, this geobarometer may prove useful for estimating metamorphic pressures. The random error of the present GBAQ geobarometer is inferred to be around ±1.8 kbar. An electronic spreadsheet is available as Table S4 to apply the GBAQ geobarometer in combination with the GB geothermometer.     

Occurrences of Ore Minerals and Fluid Inclusion Study on the Kingking Porphyry Copper–Gold Deposit, Eastern Mindanao, Philippines

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 (T_H) and the dissolution temperature of halite daughter crystals (T_M) from the polyphase hypersaline inclusions predominantly range from 400°C up to >500°C. The wide range of T_H and T_M may be due to heterogeneous trapping of variable ratios of vapor and brine. For some inclusions, T_H > T_M and in some cases, T_H < T_M, 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.     

高温变泥质岩石中石榴石-黑云母地质温度计的应用——以胶北荆山群富铝岩石为例

在对胶北荆山群麻粒岩相富铝岩石中石榴石、黑云母的成分环带进行深入研究基础上,选取不同粒径、与不同矿物相邻的石榴石、黑云母各微区点成分,利用石榴石-黑云母温度计分别进行了温度估算。确定在黑云母含量较高的岩石(V_(Grt)/V_(Bt)≤1)中,利用大颗粒石榴石(d≥1500μm)晶体核部(或靠近长英质矿物一侧的晶体幔部)成分与基质中远离石榴石等镁铁矿物处于长英质矿物之间的黑云母核部成分配合。通过石榴石-黑云母温度计可以获得相当可信的变质峰期温度。但是对于黑云母含量极低的岩石(V_(Grt)/V_(Bt)≥6),由于黑云母的成分普遍遭到了强烈改造。使得温度估算结果异常偏低,因此不适合采用石榴石-黑云母温度计估算峰期温度。同一岩石中,采用不同的相邻石榴石-黑云母矿物对晶体边缘成分获得的温度值差异较大,反映它们在峰期后发生Fe-Mg交换反应并达到封闭温度平衡状态的程度不同,因此利用石榴石-黑云母温度计难以获得准确的封闭温度。通过热力学计算,建立了一个新的石榴石-黑云母温度计公式。确定胶北荆山群所经历的变质峰期温度为720～770℃,峰期后最低相对封闭温度为480～500℃。     

Mineralogy and Mineral Chemistry of the Cretaceous Duolong Gold‐Rich Porphyry Copper Deposit in the Bangongco Arc,Northern Tibet

The Early Cretaceous Duolong gold‐rich porphyry copper deposit is a newly discovered deposit with proven 5.38 Mt Cu resources of 0.72% Cu and 41 t gold of 0.23 g t^?1 in northern Tibet. Granodiorite porphyry and quartz diorite porphyrite are the main ore‐bearing porphyries. A wide range of hydrothermal alteration associated with these porphyries is divided into potassic, argillic and propylitic zones from the ore‐bearing porphyry center outward and upward. In the hydrothermal alteration zones, secondary albite (91.5–99.7% Ab) occurs along the rim of plagioclase phenocryst and fissures. Secondary K‐feldspar (75.1–96.9% Or) replaces plagioclase phenocryst and matrix or occurs in veinlets. Biotite occurs mainly as matrix and veinlet in addition to phenocryst in the potassic zone. The biotite are Mg‐rich and formed under a highly oxidized condition at temperatures ranging from 400°C to 430°C. All the biotites are absent in F, and have high Cl content (0.19–0.26%), with log (X_Cl/X_OH) values of ?2.74 to ?2.88 and IV (Cl) values of ?3.48 to ?3.35, suggesting a significant role of chloride complexes (CuCl₂^‐ and AuCl₂^‐) in transporting and precipitating copper and gold. Chlorites are present in all alteration zones and correspond mainly to pycnochlorite. They have similar Fe/(Fe+Mg), Mn/(Mn+Mg) ratios, and a formation temperature range of 280–360°C. However, the formation temperature of chlorite in the quartz‐gypsum‐carbonate‐chlorite vein is between 190°C and 220°C, indicating that it may have resulted from a later stage of hydrothermal activity. Fe³⁺/Fe²⁺ ratios of chlorites have negative correlation with Al^IV, suggesting oxygen fugacity of fluids increases with decreasing temperature. Apatite mineral inclusions in the biotite phenocrysts show high SO₃ content (0.44–0.82%) and high Cl content (1–1.37%), indicating the host magma had a high oxidation state and was enriched in S and Cl. The highest Cl content of apatite in the propylitic zone may have resulted from pressure decrease, and the lowest Cl content of apatite in the argillic zone may have been caused by a low Cl content in the fluids. The low concentration of SO₃ content in the hydrothermal apatite compared to the magmatic one may have resulted from the decrease of oxygen fugacity and S content in the hydrothermal fluid, which are caused by the abundant precipitation of magnetite.     

湘南宝山矿床花岗闪长斑岩中黑云母的矿物学特征及其指示意义

湖南宝山矿床处于坪宝矿带的北端,是湘南地区最大的铜多金属矿床。为了进一步探讨矿区内花岗质岩石的形成条件及成矿潜力,文章在详细的野外地质和岩相学观察的基础上,对与成矿密切相关的花岗闪长斑岩中的黑云母进行了详细的矿物化学分析。电子探针分析结果表明:宝山花岗闪长斑岩中的黑云母为铁质黑云母和镁质黑云母,其中,Ti介于0.18~0.30,且Mg/(Mg+Fe2+)值介于0.42~0.58,属于典型的岩浆成因黑云母;黑云母的氧化系数为0.16~0.26,w(Mg O)为8.17%~11.72%,平均9.3%,MF值范围为0.38~0.50,指示其岩体属于壳幔混源型的I型花岗岩;岩体中以黑云母的全铝含量计算的结晶压力为97~174 MPa,相应的结晶深度为3.67~6.57 km,平均深度为5.12 km。其log f(O2)变化范围为-14.5~-12.8,表明黑云母是在较高氧逸度条件下结晶形成的,有利于铜矿的形成。     

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.     

陕西华阳川铀多金属矿床黑云母~(40)Ar/~(39)Ar年龄及其地质意义

笔者采用Ar-Ar测年技术,获得华阳川铀多金属矿床碳酸岩中黑云母~(40)Ar/~(39)Ar坪年龄132.58±0.70 Ma,等时线年龄133.01±0.74 Ma,含黑云母闪石硫化物伟晶岩中黑云母的~(40)Ar/~(39)Ar坪年龄93.72±2.38 Ma,等时线年龄91.49±1.97 Ma。镜下特征显示,铌钛铀矿的形成晚于碳酸岩中的黑云母及含黑云母闪石硫化物伟晶岩中的黑云母。因此,铌钛铀矿的形成时间应晚于93.72±2.38 Ma。这表明成矿带内除了已知存在三叠纪碳酸岩型Mo-Pb矿和白垩纪斑岩型Mo矿的成矿过程之外,还存在早白垩世之后的岩浆热液型U-Nb-Ti成矿过程。     

云南因民铁铜矿区辉长岩类中黑云母-金红石化特征及其指示意义

对云南因民铁铜矿区深部辉长岩类中金红石、黑云母、碳酸盐和绿泥石的矿物地球化学特征进行研究,以探讨赋存于辉长岩类中的铁氧化物铜金型矿(化)体的成岩成矿环境。金红石由岩浆结晶和多期蚀变作用形成,其结晶温度为820~1 082 ℃,多期蚀变温度为444~730 ℃,金红石与黑云母密切共生;黑云母可划分为原生高钛镁质黑云母、热液蚀变镁质黑云母和铁质黑云母,形成温度分别为653~750 ℃、525~619 ℃和551~577 ℃,氧逸度均位于Ni NiO缓冲剂附近,表明黑云母形成于高温强氧化环境,有利于金红石化;铁白云石-菱铁矿化揭示了强还原环境,交代蚀变金红石;绿泥石多由铁镁矿物蚀变形成,形成于中低温(174~243 ℃)、低氧逸度(-4468~-5142)和高硫逸度(-1442~-1976)的强还原环境,有利于金属硫化物形成。本区岩浆结晶演化和黑云母-金红石化蚀变具有高温强氧化地球化学岩相学特征,有利于钛、铁矿化,后期叠加中低温强还原地球化学岩相,为IOCG矿床成矿的有利地球化学岩相学类型。     

Empirical garnet–muscovite geothermometry in low-grade metapelites, Selwyn Range (Canadian Rockies)

Abstract Partitioning of Fe and Mg between garnet and phengitic muscovite was calibrated as a geothermometer by Green & Hellman (1982) using experimental data at 25–30 kbar. When the thermometer is applied to pelites regionally metamorphosed at pressures of between 3 and 7 kbar it yields temperatures much higher than those from the garnet–biotite thermometer. A new empirical calibration is proposed for use with such rocks, with particular application where garnet occurs at lower grades than biotite. The new calibration is where K is given by: In K = In K _d and X _ii are mole fractions in the garnets.
The calibration was derived from comparison with the garnet–biotite thermometer of Ferry & Spear (1978), assuming no pressure-dependence for the partitioning between garnet and muscovite, no ferric iron partitioning, ideal mixing in muscovite, and the garnet mixing model of Ganguly & Saxena (1984) modified for a non-linear Ca effect. This latter garnet mixing model was selected because it gave the geologically most reasonable results. It has not proved possible to distinguish a pressure effect from a ferric-iron effect.
Despite the simplifying assumptions used to derive the calibration, it yields temperatures generally within 15°C of those given by the garnet–biotite thermometer, and has been used to supply thermometric data in a low-grade region of the Canadian Rockies.     

Fluid inclusion studies of a new type of ore deposit: Porphyry tungsten occurrence in China

Lianhuashan mine in South China represents a new type of tungsten ore which can be described as a porphyry tungsten deposit. It is associated with a quartz porphyry stock of Yenshanian age (about 70–135 m. y.). The ore occurs in zone surrounding the contact of the quartz porphyry with Jurassic sandstone and extends into both rock bodies. The ore occurs either as the matrix of breccia or in the form of a very fine network of cross cutting veinlets. The major tungsten minerals are wolframite and scheelite associated with sulfide minerals of Mo, Fe, Cu, Pb and cassiterite. The minerals are fine-grained. There is zoned alteration in the wall rocks. From the center of the quartz porphyry toward the wall rocks one finds: potassic alteration, silicification-sericitization, and chloritization. All these features are similar to those of porphyry copper mineralization. Fluid inclusion studies show three types of inclusion: liquid-rich (Type I), gas-rich (Type II), and polyphase with daughter minerals (Type III) fluid inclusions. The homogenization temperatures of Type I range from 210° to 380°C, with a salinity of 2–15 wt.% NaCl equiv., those of Type II from 270° to 420°C, and those of Type III from 240° to 400°C with a salinity of 31–33 wt.% NaCl equiv. The closely associated group of gas-rich and daughter mineral-bearing fluid inclusions homogenized at almost the same temperatures. Such results indicate boiling of oreforming fluids. These fluid inclusion data indicate that low salinity (Type I) and high salinity fluids (Type III) responsible for porpb yry copper deposits are the same as those for porphyry tungsten ore deposits. These observations suggest that the Lianhuashan tungsten ore deposit is a porphyry tungsten deposit and was formed by hydrothermal fluids similar to those responsible for the well-known porphyry copper deposits.     

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.     

Characteristic Features of REE and Pb–Zn–Ag Mineralizations in the Na Son Deposit,Northeastern Vietnam

The Na Son deposit is a small‐scale Pb–ZnPb–Zn–Ag deposit in northeast Vietnam and consists of biotite–chlorite schist, reddish altered rocks, quartz veins and syenite. The biotite–chlorite schist is intruded by syenite. Reddish altered rocks occur as an alteration halo between the biotite–allanite‐bearing quartz veins and the biotite–chlorite schist. Allanite occurs in the biotite–allanite‐bearing quartz veins and in the proximal reddish altered rocks. Rare earth element (REE) fluorocarbonate minerals occur along fractures or at rim of allanite crystals. The later horizontal aggregates of sulfide veins and veinlets cut the earlier reddish altered rocks. The earlier Pb–Zn veins consist of a large amount of galena and lesser amounts of sphalerite, pyrite and molybdenite. The later Cu veins cutting the Pb–Zn veins include chalcopyrite and lesser amounts of tetrahedrite and pyrite. The occurrences of two‐phase H₂O–CO₂ fluid inclusions in quartz from biotite–allanite‐bearing quartz veins and REE‐bearing fluorocarbonate minerals in allanite suggest the presence of CO₂ and F in the hydrothermal fluid. The oxygen isotopic ratios of the reddish altered rocks, biotite–chlorite schist, and syenite range from +13.9 to +14.9 ‰, +11.5 to +13.3 ‰, and +10.1 to +11.6 ‰, respectively. Assuming an isotopic equilibrium between quartz (+14.6 to +15.8 ‰) and biotite (+8.6 ‰) in the biotite–allanite‐bearing quartz vein, formation temperature was estimated to be 400°C. At 400°C, δ¹⁸O values of the hydrothermal fluid in equilibrium with quartz and biotite range from +10.5 to +11.7 ‰. These δ¹⁸O values are consistent with fluid that is derived from metamorphism. Assuming an isotopic equilibrium between galena (+1.5 to +1.7 ‰) and chalcopyrite (+3.4 ‰), the formation temperature was estimated to be approximately 300°C. The formation temperature of the Na Son deposit decreased with the progress of mineralization. Based on the geological data, occurrence of REE‐bearing minerals and oxygen isotopic ratios, the REE mineralization is thought to result from interaction between biotite–chlorite schist and REE‐, CO₂‐ and F‐bearing metamorphic fluid at 400°C under a rock‐dominant condition.     

新疆玉海-三岔口铜矿黑云母矿物化学特征及成岩成矿意义

黑云母的化学成分对于揭示结晶条件、岩石成因、成矿演化以及含矿性评价等具有重要的指示意义.利用电子探针（EPMA）对新疆玉海和三岔口铜矿中的黑云母进行成分分析,结果表明与成矿相关岩体的黑云母具有富镁贫铁的特征,而无矿化岩体中的黑云母则呈现富铁贫镁的特征.分析结果显示矿化岩体中黑云母为再平衡镁质黑云母,而无矿化岩体中黑云母为原生铁质黑云母;它们的寄主岩石均属于I型花岗岩,形成于与俯冲相关的构造背景,但是与矿化相关岩体的岩浆源区为壳幔混合来源,而无矿岩体的源区为地壳来源,形成过程中有新生地壳组分的混染;两类黑云母的结晶温度为529~677 ℃,寄主岩体的固结压力为1.1~2.8 kbar,均形成于高氧逸度条件;此外,黑云母的Mg/Fe和Fe2+/（Fe2++Mg2+）还可以区分斑岩型铜矿的含矿性.      

Advances in Research of Mineral Chemistry of Magmatic and Hydrothermal Biotites

Biotite is an important hydrated ferromagnesian silicate mineral in igneous rocks and porphyry deposits. The determination of chemical compositions of biotite plays an important role in both igneous petrology and ore forming processes. This paper summarizes research results of magmatic and hydrothermal biotites exemplified by the Lakange porphyry Cu–Mo deposit and the Qulong porphyry Cu deposit in the Gangdese porphyry–skarn metallogenic belt, Tibet. Biotite mineral chemistry can provide critical insights into classification, geothermometer, geothermobarometry, oxygen fugacity, petrogenesis and tectonic setting, evaluating magmatic-hydrothermal process by halogen and halogen fugacity ratios, and distinguishing between barren and mineralized rocks. Biotite provides the latest mineralogical evidence on metallogenic prognosis and prospecting evaluation for porphyry Cu polymetallic deposits or magmatic hydrothermal deposits.     

Rb–Sr Dating of Gold‐Bearing Pyrite in the Jinchang Porphyry Cu–Au Deposit,Heilongjiang Province,NE China

The Jinchang Cu–Au deposit in Heilongjiang Province, NE China, is located in the easternmost part of the Central Asian Orogenic Belt. Rb–Sr analyses of auriferous pyrite from the deposit yielded an isochron age of 113.7 ±2.5 Ma, consistent with previously reported Re–Os ages. Both sets of ages represent the timing of Cu–Au mineralization because (i) the pyrite was separated from quartz–sulfide veins of the mineralization stage in granite porphyry; (ii) fluid inclusions have relatively high Rb, Sr, and Os content, allowing precise measurement; (iii) there are no other mineral inclusions or secondary fluids in pyrite to disturb the Rb–Sr or Re–Os decay systems; and (iv) the closure temperatures of the two decay systems are ≥500°C (compared with the homogenization temperatures of fluid inclusions of 230–510°C). It is proposed that ore‐forming components were derived from mantle–crust mixing, with ore‐forming fluids being mainly exsolved from magmas with minor amounts of meteoric water. The age of mineralization at Jinchang and in the adjacent regions, combined with the tectonic evolution of the northeast China epicontinental region, indicates that the formation of the Jinchang porphyry Cu–Au deposit was associated with Early Cretaceous subduction of the paleo‐Pacific Plate.     

Constraining the timing of porphyry mineralization in northwest Iran in relation to Lesser Caucasus and Central Iran; Re–Os age data for Sungun porphyry Cu–Mo deposit

The Neo-Tethyan subduction in Iran is characterized by the Urumieh–Dokhtar magmatic arc (UDMA), formed by northeast-ward subduction of the oceanic crust beneath the central Iran. This belt coincides with the porphyry copper metallogenic belt that comprises several metallogenic zones, including Ahar–Jolfa in northwest Iran. The Ahar–Jolfa metallogenic zone encompasses two main batholiths of Qaradagh and Sheyvardagh and numerous intrusive bodies of Cenozoic, which have produced many base and precious metal deposits and prospects. The former is considered as continuation of the Meghri–Ordubad pluton in South Armenian Block (SAB), which also hosts porphyry copper deposits (PCDs). The Sungun PCD is the largest occurrence in northwest Iran. Rhenium-Osmium ages of Sungun molybdenites are early Miocene and range between 22.9 ± 0.2 and 21.7 ± 0.2 Ma. Comparison of the ages obtained here with published ages for mineralization across the region suggests the following sequence. The earliest porphyry Cu–Mo mineralization event in northwest Iran is represented by Saheb Divan PCD of late Eocene age, which is followed by the second epoch of middle Oligocene, including the Cu–Mo–Au mineralization at Qarachilar and the Haftcheshmeh PCD. Mineralization in Sungun, Masjed Daghi, Kighal and Niaz deposits corresponds to the third mineralization event in northwest Iran. The first epoch in northwest Iran postdates all Eocene mineralizations in SAB, while the second epoch is coeval with Paragachay and the first-stage of Kadjaran PCDs. Its third epoch is younger than all mineralizations in SAB, except the second stage in Kadjaran PCD. Finally, the Cu mineralization epochs in northwest Iran are older than nearly all PCDs and prospects in Central Iran (except the Bondar Hanza PCD), altogether revealing an old to young trend along the UDMA and the porphyry Cu belt towards southeast, resulted from diachronous, later closure of the Neo-Tethyan oceanic basin in central and SE Iran.     

Recalibration of mutually consistent garnet–biotite and garnet–cordierite geothermometers

Garnet–biotite and garnet–cordierite geothermometers have been consistently calibrated, using the results of Fe²⁺–Mg cation exchange experiments and utilizing recently evaluated nonideal mixing properties of garnet. Nonideal mixing parameters of biotite (including Fe, Mg, Al^VI, and Ti) and of cordierite (involving Fe and Mg) are evaluated in terms of iterative multiple least-square regressions of the experimental results. Assuming the presence of ferric Fe in biotite in relation to the coexisting Fe-oxide phases (Case A), and assuming the absence of ferric Fe in biotite (Case B), two formulae of garnet–biotite thermometer have been derived. The garnet–cordierite geothermometer was constructed using Margules parameters of garnet adopted in the garnet–biotite geothermometers. The newly calibrated garnet–biotite and garnet–cordierite thermometers clearly show improved conformity in the calculated temperatures. The thermometers give temperatures that are consistent with each other using natural garnet–biotite–cordierite assemblages within ±50 °C. The effects of ferric Fe in biotite on garnet–biotite thermometry have been evaluated comparing the two calibrations of the thermometer. The effects are significant; it is clarified that taking ferric Fe content in biotite into account leads to less dispersion of thermometric results.