Hydrothermal evolution of the Sar-Cheshmeh porphyry Cu–Mo deposit, Iran: Evidence from fluid inclusions

The Sar-Cheshmeh porphyry Cu–Mo deposit is located in Southwestern Iran (65 km southwest of Kerman City) and is associated with a composite Miocene stock, ranging in composition from diorite through granodiorite to quartz-monzonite. Field observations and petrographic studies demonstrate that the emplacement of the Sar-Cheshmeh stock took place in several pulses, each with associated hydrothermal activity. Molybdenum was concentrated at a very early stage in the evolution of the hydrothermal system and copper was concentrated later. Four main vein Groups have been identified: (I) quartz+molybdenite+anhydrite±K-feldspar with minor pyrite, chalcopyrite and bornite; (II) quartz+chalcopyrite+pyrite±molybdenite±calcite; (III) quartz+pyrite+calcite±chalcopyrite±anhydrite (gypsum)±molybdenite; (IV) quartz±calcite±gypsum±pyrite±dolomite. Early hydrothermal alteration produced a potassic assemblage (orthoclase-biotite) in the central part of the stock, propylitic alteration occurred in the peripheral parts of the stock, contemporaneously with potassic alteration, and phyllic alteration occurred later, overprinting earlier alteration. The early hydrothermal fluids are represented by high temperature (350–520 °C), high salinity (up to 61 wt% NaCl equivalent) liquid-rich fluid inclusions, and high temperature (340–570 °C), low-salinity, vapor-rich inclusions. These fluids are interpreted to represent an orthomagmatic fluid, which cooled episodically; the brines are interpreted to have caused potassic alteration and deposition of Group I and II quartz veins containing molybdenite and chalcopyrite. Propylitic alteration is attributed to a liquid-rich, lower temperature (220–310 °C), Ca-rich, evolved meteoric fluid. Influx of meteoric water into the central part of the system and mixing with magmatic fluid produced albitization at depth and shallow phyllic alteration. This influx also caused the dissolution of early-formed copper sulphides and the remobilization of Cu into the sericitic zone, the main zone of the copper deposition in Sar-Cheshmeh, where it was redeposited in response to a decrease in temperature.     

赤峰敖仑花钼铜矿床地质特征及找矿标志

敖仑花斑岩钼铜矿床位于大兴安岭南段,是西拉木伦河断裂北侧成矿带新发现的大型斑岩型钼铜矿床,敖仑花铜钼矿主要赋存于斜长花岗斑岩中,硅化、钾长石化、黄铁矿化等蚀变发育,并具有明显的分带特征,石英网脉极为发育,网脉的密度可指示矿化作用的强度。本文在分析矿床的成矿地质背景、矿床的地质、地球物理和地球化学特征,从横向和垂向上测量石英网脉密度的变化规律以及蚀变分带规律的基础上,总结矿床的找矿标志,指导成矿预测。     

Origin of the Matauri Bay halloysite deposit, Northland, New Zealand

At the Matauri Bay halloysite deposit, economically valuable halloysite-rich clays are hosted by a sanidine rhyolite dome (Ar–Ar dated at 10.1?±?0.03?Ma). The rhyolite dome intrudes an older basalt and is overlain by alluvial sediments and a younger basalt (4.0?±?0.7?Ma). A blanket-like, halloysite-rich zone is restricted to depths of 10–30?m from the present day erosion surface. Primary sanidine and plagioclase phenocrysts in rhyolite are completely leached out in the halloysite-rich zone but are only partially leached out at greater depth. Halloysite was formed by hydrolysis and cation leaching of sanidine and plagioclase phenocrysts and groundmass glass in the rhyolite, resulting in loss of K, Ca, Na and Si and enrichment in OH (LOI 6–10%) and Al₂O₃ (20–30%) relative to least-altered rhyolite with 1.8% LOI and 14.5% Al₂O₃. Oxygen and hydrogen isotope data indicate the halloysite is supergene rather than hydrothermal in origin, which is consistent with the absence of pyrite, alunite and other acid-sulphate type hydrothermal minerals, and with the blanket-like alteration profile. The dominance of halloysite over kaolinite was favoured by water-saturated weathering conditions during the late Miocene-Pliocene subtropical weathering regime in Northland.     

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

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

湖北铜绿山矽卡岩型铜铁矿床中隐爆角砾岩型金（铜）矿体的发现及其找矿前景

经研究确认鄂东南铜绿山矿床为隐爆角砾岩型金(铜)矿。这一新类型的金(铜)矿体受NWW向断裂、隐爆角砾岩带、接触带复合构造的控制,产于矽卡岩型矿体上盘大理岩残留体的边部,走向上大致与NNE向矽卡岩型主矿带垂直。矿石呈角砾状构造,角砾成分为大理岩、斜长石岩,含少量块状磁铁矿矿石角砾和高岭石化花岗岩角砾。胶结物主要为细碎屑物及微细粒状石英、玉髓、高岭石、黄铜矿和黄铁矿等中低温热液矿物。矿石平均wCu2.54%,wAu3.44×10-6。隐爆角砾岩型矿化是在岩浆侵入作用下成矿热液演化晚期阶段形成的,时间上晚于矽卡岩型,但可叠加其上,常形成富铜金矿体,也可形成独立金矿体。隐爆角砾岩型金(铜)矿体的发现为大幅度增加铜绿山矿床的储量指明了方向,对认识铜绿山矿田的成矿系列具有重要意义。     

Lewis Ponds, a hybrid carbonate and volcanic-hosted polymetallic massive sulphide deposit, New South Wales, Australia

The Lewis Ponds Zn–Pb–Cu–Ag–Au deposit, located in the eastern Lachlan Fold Belt, central western New South Wales, exhibits the characteristics of both volcanic-hosted massive sulphide and carbonate-hosted replacement deposits. Two stratabound massive to disseminated sulphide zones, Main and Toms, occur in a tightly folded Upper Silurian sequence of marine felsic volcanic and sedimentary rocks. They have a combined indicated resource of 5.7 Mt grading 3.5% Zn, 2.0% Pb, 0.19% Cu, 97 g/t Ag and 1.9 g/t Au. Main Zone is hosted by a thick unit of poorly sorted mixed provenance breccia, limestone-clast breccia and quartz crystal-rich sandstone, whereas Toms Zone occurs in the overlying siltstone. Pretectonic carbonate–chalcopyrite–pyrite and quartz–pyrite stringer veins occur in the footwall porphyritic dacite, south of Toms Zone. Strongly sheared dolomite–chalcopyrite–pyrrhotite veins directly underlie the Toms massive sulphide lens. The mineralized zones consist predominantly of pyrite, sphalerite and galena. Paragenetically early framboidal, dendritic and botryoidal pyrite aggregates and tabular pyrrhotite pseudomorphs of sulphate occur throughout the breccia and sandstone beds that host Main Zone, but are rarely preserved in the annealed massive sulphide in Toms Zone. Main and Toms zones are associated with a semi-conformable hydrothermal alteration envelope, characterized by texturally destructive chlorite-, dolomite- and quartz-rich assemblages. Dolomite, chlorite, quartz, calcite and sulphides have selectively replaced breccia and sandstone beds in the Main Zone host sequence, whereas the underlying porphyritic dacite is weakly sericite altered. Vuggy and botryoidal textures resulted from partial dissolution of the dolomite-altered sedimentary rocks and unimpeded growth of base metal sulphides, carbonate and quartz into open cavities. The intense chlorite-rich alteration assemblage, underlying Toms Zone, grades outward into a weak pervasive sericite–quartz assemblage with distance from the massive sulphide lens. Limestone clasts and hydrothermal dolomite at Lewis Ponds are enriched in light carbon and oxygen isotopes. The dolomite yielded ¹³C_VPDB values of –11 to +1 and ¹⁸O_VSMOW values of 6 to 16. Liquid–vapour fluid inclusions in the dolomite have low salinities (1.4–7.7 equiv. wt% NaCl) and homogenization temperatures (166–232°C for 1,000 m water depth). Dolomitization probably involved fluid mixing or fluid–rock interactions between evolved heated seawater and the limestone-bearing facies, prior to and during mineralization. ³⁴S_VCDT values range from 2.0 to 5.0 in the massive sulphide and 3.9 to 7.4 in the footwall carbonate–chalcopyrite–pyrite stringer veins, indicating that the hydrothermal fluid may have contained mamgatic sulphur and a component of partially reduced seawater. The sulphide mineral assemblages at Lewis Ponds are consistent with moderate to strongly reduced conditions during diagenesis and mineralization. Low temperature dolomitization of limestone-bearing facies in the Main Zone host sequence created secondary porosity and provided a reactive host for fluid-rock interactions. Main Zone formed by lateral fluid flow and sub-seafloor replacement of the poorly sorted breccia and sandstone beds. Base metal sulphide deposition probably resulted from dissolution of dolomite, fluid mixing and increased fluid pH. Pyrite, sphalerite and galena precipitated from a relatively low temperature, 150–250°C hydrothermal fluid. In contrast, Toms Zone was emplaced into fine-grained sediment at or near the seafloor, above a zone of focused up-flowing hydrothermal fluids. Copper-rich assemblages were deposited in the Toms Zone footwall and massive sulphide lenses in Main and Toms zones as the hydrothermal system intensified. During the D₁ deformation, fracture-controlled fluids within the Lewis Ponds fault zone and adjacent footwall volcanic succession remobilized sulphides into syntectonic quartz veins. Lewis Ponds is a rare example of a synvolcanic sub-seafloor hydrothermal system developed within fossiliferous limestone-bearing facies. The close spatial association between limestone, hydrothermal dolomite, massive sulphide and dacite provides a basis for new exploration targets elsewhere in New South Wales.Editorial handling: D. Lentz     

Mineral-chemistry and stable-isotope constraints on the magmatism, hydrothermal alteration, and related PGE–(base-metal sulphide) mineralisation of the Mesoarchaean Baula-Nuasahi Complex, India

The Baula-Nuasahi Complex, on the southern flank of the Singhbhum Archaean nucleus in north-eastern India, exposes a series of Mesoarchaean igneous suites. These are (1) a gabbro–anorthosite unit, which is petrographically homogeneous, although mineral-chemistry data hint at a subtle eastward differentiation; (2) a peridotite unit (with three chromitite layers) together with (3) a pyroxenite unit which display cumulate textures, modal layering, and (for the peridotite unit) differentiation trends in both mineralogy and mineral chemistry; and (4) the Bangur gabbro (~3.1 Ga), which defines an oblong intrusion, crosscutting the older igneous suites in the southern part of the complex, with a curvilinear NW-trending apophysis, 2 km long and up to 40 m wide. Magmatic breccia comprising ultramafic and chromitite wall-rock clasts in a gabbro matrix is exposed at the contact of the main Bangur gabbro body and also forms the entire Bangur gabbro apophysis. Concentrations of platinum-group minerals (PGMs) are found where the breccia contains abundant chromitite clasts, and two types of platinum-group-element (PGE) mineralisation are recognised. Type 1 (Pt 1.1–14.2, Pd 0.1–2.1 ppm, with an average Pt/Pd=8–9) is a contact-type mineralisation which occurs in the breccia at the contact between the Bangur intrusion and its ultramafic host. The PGMs—Pt alloys (isoferroplatinum) and sulphides (braggite, malanite)—are enclosed by pyroxene and plagioclase, reflecting a magmatic origin. Significant wall-rock assimilation by the magma (giving rise to the Bangur gabbro) is indicated by changes in pyroxene composition and by the presence of relicts of chromite (from the host) now altered to secondary ferritchromite in the contact zone. Type 2 PGE mineralisation (Pt 0.3–1.6, Pd 1.8–6.0 ppm, with Pt/Pd~0.5–3.0) is restricted to the breccia apophysis of the Bangur gabbro where it occurs in the breccia matrix, associated with an intense hydrothermal alteration which does not exist in the contact zone. PGMs (PGE arsenides, tellurides, bismuthides and antimonides) and, where present, base-metal sulphides (BMSs) form intergrowths with hydrous silicates, reflecting a hydrothermal origin. Oxygen isotope geothermometry documents the main stages of hydrothermal alteration within a decreasing temperature range between 700–1,000 and 500–600 °C, and oxygen, hydrogen and sulphur isotopes show that the hydrothermal fluids were derived from the magma rather than an external source. Pervasive hydrothermal alteration in the breccia apophysis likely represents upward channelling of late-magmatic fluids along a narrow, near-vertical, subplanar conduit which led away from the main magma chamber. We suggest that Type 2 mineralisation was produced by late-magmatic hydrothermal remobilisation and reconcentration of Type 1 PGE mineralisation, and that the composition of the hydrothermal fluids controlled whether BMSs were enriched along with the PGMs.Editorial handling: P. Lightfoot     

Geology of the mineralized zone of the Wanapitei complex,Grenville Front,Ontario

The Wanapitei Complex (6 km×2.5 km), lying 0.4 km southeast of the Grenville Front, consists of a northwestern zone of gabbro and folded injection breccia and a southeastern layer of intensely folded hornblendeplagioclase gneiss. Disseminated Ni-Cu sulphides are unevenly distributed in a zone between the injection breccia and the folded gneiss.Rocks of the mineralized zone occur in southeastern and northeastern areas. The former area consists of hornblende norite, the major host rock of the sulphides, and olivine norite. Steeply-dipping cross-bedded primary layers and chemical trends indicate the top faces southeast. In the latter area olivine norite, hornblende norite, and hornblende gabbro grade eastward into recrystallized rocks and breccia. The olivine norites are characterized by corona reaction rims. Reactions are: olivine+plagioclase bronzite+diopside-spinel; olivine+pyroxene bronzite; and pyroxene+plagioclase diopside-spinel. Molecular proportion ratio variation diagrams suggest that rocks evolved from a common parent magma that underwent fractionation dominated by olivine and plagioclase. Sulphide mineralization (pyrrhotite, chalcopyrite, pentlandite, pyrite) is interstitial to the silicates and appears to be of primary magmatic origin.Northeasterly-trending shear zones, felsic dikes, and matic dikes are metamorphosed to the same degree as the rocks they cut (amphibolite facies). The sequence of events for the mineralized zone are: intrusion deep in the crust; tilting; brecciation; shearing; felsic and mafic dike emplacement; metamorphism; and injection of granite pegmatite dikes.Deceased (8-16-1986)     

Geology and geochemistry of the Changba SEDEX Pb-Zn deposit,Qinling orogenic belt,China

The Changba Pb-Zn SEDEX deposit occurs in the Middle Devonian sequence of the Anjiaca Formation of the Western Qinling Hercynian Orogen in the Gansu Province, China. The Changba-II orebody is hosted in biotite quartz schist and is the largest of 143 stratiform orebodies that are hosted either in biotite quartz schist or marble. The Changba-II comprises two types of mineralization: a bedded facies and an underlying breccia lens. The bedded section exhibits three sulfide sub-facies zoned from bottom to top: 1) banded sphalerite intercalated with quartz albitite; 2) interbedded massive pyrite and sphalerite ore; and 3) banded sphalerite ore intercalated with banded baritite. Major metallic minerals are sphalerite, pyrite, galena, with minor arsenopyrite, pyrrhotite, boulangerite, and rare chalcopyrite. The bedded sulfides are underlain by a lens of brecciated and albitized biotite-quartz schists cemented by sulfides and tourmaline.Massive and bedded sulfide ³⁴S values range from 8.1 to 29.3, whereas barite ³⁴S values range from 20.8 to 31.5. Disseminated pyrite in footwall schists has ³⁴S values ranging from 8.1 to 10.6, and increase to values ranging from 11.1 to 14.7 in the hangingwall. The lower ³⁴S values for massive and bedded sulfides are interpreted to be derived from progressive bacterial sulfate reduction (BSR) of Devonian seawater in a sulfate-restricted sub-basin. The higher ³⁴S values for massive and bedded sulfides could be a product of quantitative BSR but this is incompatible with barite being more abundant above the bedded sulfides. Instead, it is more likely that thermochemical sulfate reduction of seawater sulfate or of evaporite was the source of heavy hydrothermal sulfur. Heavy hydrothermal sulfur was injected into a sulfate-restricted sub-basin where it mixed with low ³⁴S BSR sulfide to form the massive and bedded sulfides. The REE patterns of sulfide layers and associated quartz albitite and baritite are similar to those of the host biotite quartz schists, suggesting that the hydrothermal fluids leached REE from the underlying rocks. Pb isotope ratios in galena form an array between the Upper Crust and the Mantle reservoir curves, which indicates that the lead is derived from upper crustal rocks comprising mafic igneous units. The Sr⁸⁷/Sr⁸⁶ ratio of 0.7101 for carbonate within the sulfide layers also suggests that Sr is derived from the mixing of Sr leached from upper crustal rocks with Middle Devonian seawater Sr. A Rb-Sr isochron age of 389.4 ± 6.4 Ma for sulfide layers and the interbedded hydrothermal sediments is consistent with the age of host Mid-Devonian strata. Ar³⁹/Ar⁴⁰ plateau age at 352.8 ± 3.5 Ma and Ar³⁹-Ar⁴⁰ isochron age of 346.6 ± 6.4 Ma for albite in the quartz albitite intercalated with sulfide layers indicate either albite formation after the sulfides or thermal resetting of the Rb-Sr system at about 350 Ma, the age of collision between the North China and Yangtze cratons.Editorial handling: E. Frimmel     

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

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

福建武夷山坪地钼矿辉钼矿铼-锇同位素定年及其地质意义

福建武夷山坪地钼矿为中高温热液型钼矿,产于晚侏罗世钾长花岗岩岩体"层节理"及岩体与下元古界大金山组接触带的南北向断裂中。矿石自然类型主要为硅化岩型(石英脉型)、黄铁绢英岩型、花岗岩型、蚀变构造岩型。矿石构造主要有条带状、浸染状、角砾状、细脉状等构造类型。矿石结构以中粗-中细粒鳞片结构为主,局部呈现厚板状、带状(常常弯曲)。辉钼矿是唯一的矿石矿物。本研究采集坪地钼矿不同矿体、不同产状、不同标高的辉钼矿进行Re-Os同位素测年,得到等时线年龄为(102.9±1.8)Ma,MSWD=2.1,Re-Os模式年龄为(103.70±1.7)Ma～(111.6±1.6)Ma,加权平均值为(107.4±3.3)Ma,MSWD=16。MSWD均较大,说明坪地辉钼矿的成矿具有多阶段性,钾长花岗岩中细脉状、岩体"层节理"中粗脉状和断裂角砾岩带中团块状三种类型的辉钼矿分别是在(111.20±1.7)Ma～(111.60±1.6)Ma、(105.60±1.6)Ma～(107.40±1.6)Ma和(103.70±1.7)Ma三个不同的成矿阶段形成的,成矿时代属早白垩世晚期。这一同位素年龄资料为福建东南沿海浦城—宁德北西向中生代构造-岩浆带中同类矿床的形成演化与指导区域找矿提供了新的地球化学依据。     

Silikatische Kupferlagerstätten in Nordchile

The formation of isolated silicateous copper deposits is controlled by two main conditions:

1. oversaturation of groundwaters in silica
2. lateral inflow of copper bearing and slightly acid solutions originating from the oxidation of primary sulfide deposits.

The basic copper silicate chrysocolla is formed by chemisorption of copper ions by disilicic acid with a net-like structure. Under favourable conditions copper silicate deposits are formed which contain up to several million tons of copper as for example the La Exotica deposit in Northern Chile. The copper values of these deposits sometimes exceed those of the primary sulfide deposits. Thus, the oxidation of sulfide deposits, the migration of copper bearing solutions and the chemisorption of copper ions by the disilicic acid can result in workable new copper concentrations originating from sulfide protores. High concentrations of silica in groundwaters and thus the chemisorption of copper ions by the disilicic acid as an ore forming process is restricted to arid or semiarid regions. Therefore it is proposed to call such deposits arid silicateous infiltration deposits. Infiltration deposits are related to weathering processes. “They comprise products of weathering by which valuable substances were leached from the host rocks, migrated in groundwaters and were redeposited in other neighbouring rocks” (Smirnov, 1970, p. 324).     

小秦岭地区大湖-秦南钼矿床矿化类型、Re-Os定年及找矿方向

小秦岭地区大湖—秦南钼矿床位于华北地台南缘,属于小秦岭-外方山成矿亚带。矿化类型可分为含钼次生石英岩型和细脉浸染型。含钼次生石英岩型矿石构造有角砾状构造、团块状构造、蜂窝状构造、细脉网脉状构造和块状构造;蚀变以细脉浸染状钾化、硅化、碳酸盐化、高岭土化、硬石膏化为特征。细脉浸染型矿化通常与花岗质岩石关系密切,偶尔也见于含钼次生石英脉边部的片麻岩中;蚀变通常为钾化、硅化、绢云母化和少量的黄铁矿化、高岭土化、碳酸盐化等。含钼次生石英岩型含有含钼花岗质岩石角砾。野外证据表明,含钼花岗质岩石向含钼次生石英岩内部表现为,含钼花岗质岩石角砾逐渐变小,并逐渐被含钼次生石英岩包裹,含钼石英脉增厚,高岭土化、硬石膏化增强。这一特征反映了二者之间的成因联系。两种矿化类型中获得的12件辉钼矿Re-Os模式年龄分别为（223.6±4.1）~（196.1±3.0）Ma以及（197.8±3.2）和（196.1±3.3）Ma,Re-Os同位素等时线年龄为（199+14/-25）Ma。这些年龄数据表明,该区的成矿作用发生于印支期或早燕山期。钼矿化时空上与花岗斑岩脉和正长斑岩一致,含钼花岗质岩石的矿化和蚀变样式与斑岩型矿床类似。辉钼矿中w（Re）为0.894×10^-6~2.964×10^-6,反映钼成矿物质来源于地壳。这一时期,区域上以碱性岩岩脉产出为特征,因此本区成矿作用形成于陆内伸展环境下,应注意找寻与印支期花岗质岩石有关的斑岩型钼矿床。     

The high-pressure assemblages at Milos,Greece

Metamorphic rocks at Milos are known in small outcrops beneath the volcanic formations, as xenoliths in the Traphores volcanic breccia and as pebbles in the Paleochora Quaternary deposits. These rocks seem to belong to three different metamorphic units which probably have intricate relationships in the basement: — the eclogites unit shows garnetjadeite or garnet-omphacite primary associations, with apparently late crystallization of lawsonite phenoblasts an recrystallization features at relatively low temperatures; — the glaucophane schist unit exhibits Jadeite+quartz or glaucophane+lawsonite primary mineralogy; — the greenschist facies unit shows low-pressure main assemblages, most generally developed after high-pressure events. The two former units involve tholeiitic meta-igneous rocks, having been spilitized before metamorphism; they generally suffered more or less advanced recrystallization features in the low-pressure field of the greenschist facies. The third unit shows only meta-sedimentary rocks, with the sole exception of one single meta-doleritic pebble having calk-alkaline affinities.Petrological and mineralogical studies, based upon 15 bulk-rock compositions and 178 probe-analysed data points, lead to suspect at least 2, perhaps 3, different metamorphic events rather than one single metamorphic evolution, to account for the 3 U distinguished. From the observation of the mineralogical assemblages and their evolution, the former events (stages 1 and 2) could be related to rapid subduction of ocean-floor or back-arc basalts, whereas, during the latter event (stage 3), the rocks experienced crystallization conditions involving both decreasing pressures and increasing temperatures.     

Stable isotope (C,O, S) systematics of the mercury mineralization at Idrija,Slovenia: constraints on fluid source and alteration processes

The world-class Idrija mercury deposit (western Slovenia) is hosted by highly deformed Permocarboniferous to Middle Triassic sedimentary rocks within a complex tectonic structure at the transition between the External Dinarides and the Southern Alps. Concordant and discordant mineralization formed concomitant with Middle Triassic bimodal volcanism in an aborted rift. A multiple isotopic (C, O, S) investigation of host rocks and ore minerals was performed to put constraints on the source and composition of the fluid, and the hydrothermal alteration. The distributions of the ¹³C and ¹⁸O values of host and gangue carbonates are indicative of a fracture-controlled hydrothermal system, with locally high fluid-rock ratios. Quantitative modeling of the ¹³C and ¹⁸O covariation for host carbonates during temperature dependent fluid-rock interaction, and concomitant precipitation of void-filling dolomites points to a slightly acidic hydrothermal fluid (¹³C–4 and ¹⁸O+10), which most likely evolved during isotopic exchange with carbonates under low fluid/rock ratios. The ³⁴S values of hydrothermal and sedimentary sulfur minerals were used to re-evaluate the previously proposed magmatic and evaporitic sulfur sources for the mineralization, and to assess the importance of other possible sulfur sources such as the contemporaneous seawater sulfate, sedimentary pyrite, and organic sulfur compounds. The ³⁴S values of the sulfides show a large variation at deposit down to hand-specimen scale. They range for cinnabar and pyrite from –19.1 to +22.8, and from –22.4 to +59.6, respectively, suggesting mixing of sulfur from different sources. The peak of ³⁴S values of cinnabar and pyrite close to 0 is compatible with ore sulfur derived dominantly from a magmatic fluid and/or from hydrothermal leaching of basement rocks. The similar stratigraphic trends of the ³⁴S values of both cinnabar and pyrite suggest a minor contribution of sedimentary sulfur (pyrite and organic sulfur) to the ore formation. Some of the positive ³⁴S values are probably derived from thermochemical reduction of evaporitic and contemporaneous seawater sulfates.Editorial handling: P. Lattanzi     

西藏沙让钼矿首采地段地质特征研究

沙让钼矿是近年来新发现的斑岩型辉钼矿床,于斜长花岗斑岩体的构造破碎带中形成细脉状、网脉状矿脉,后期热液作用明显,矿体总体呈近东西走向。矿石工业类型属原生硫化钼矿,金属矿物主要为辉钼矿、黄铁矿、钛铁矿。辉钼矿呈片状、粒状、粉末状分布于矿石中,其单晶粒度≤0.1 mm～2 mm,矿体Mo平均含量为0.038×10-2～0.222×10-2,单样最高含量为3.35×10-2。依据含矿岩体岩石化学分析,这里指出在碰撞过程和后造山过程中,由于重熔岩浆与地壳物质混染程度不同,以及重熔岩浆分异程度差异较大,因此形成了矿区含矿岩体既不同于典型的S型,也不同于典型I型岩浆岩的特征。     

Geology and geochemistry of the Mendejin plutonicrocks, Mianeh, Iran

The Mendejin pluton is located in the Mianeh area, NW Iran, 550 km from Tehran. This pluton is probably of Oligo-Miocene age and is the result of extensive magmatism which occurred during and after the Alpine Orogeny. Similar plutons are common in the Alborz–Azarbaijan structural zone of Iran, and it is likely that there are concealed plutons related to this extensive Cenozoic magmatism, but due to their youth and low rates of erosion they have not yet been exposed. The Mendejin pluton is a composite body made up of four types of plutonic rocks: pink tonalite, grey tonalite, diorite and aplite. The pink tonalite is porphyritic and contains phenocrysts of plagioclase, K-feldspar and hornblende in a groundmass consisting of quartz, plagioclase, K-feldspar, hornblende, zircon, monazite, leucoxene, apatite and hematite. The grey porphyritic tonalite has more biotite, pyroxene and pyrite and less accessory phases compared with the pink tonalite. The diorite has a microporphyritic texture with phenocrysts of plagioclase, hornblende and augite. This rock also occurs as xenoliths in the Mendejin pluton. The aplitic dykes are the youngest magmatic products at Mendejin. The Mendejin tonalite contains more Cl, As, S, Cu, Ni and Zn than the global granite. These rocks are of I-type, peraluminous and calc-alkaline, with medium to high potassium, and were formed as part of a volcanic arc. The Mendejin pluton contains up to 8 ppb gold and could potentially have been the source of an economic gold deposit by leaching of Au from wall rocks and deposition in extensive hydrothermally altered marginal zones.     

铁米尔特——恰夏——萨热阔布多金属金矿床系列矿床地质地球化学研究

铁米尔特－－恰夏－－萨热阔布多金属金矿田已发现铁米尔特铜铅锌矿床、恰夏铜矿床、萨热阔布金矿床，组成了矿田的矿床系列。早泥盆世火山活动于近火山口附近形成了与火山喷气热液有关的恰夏黄铁矿型铜矿床；于火山洼地中形成与火山沉积作用有关的铁米尔特铜铅锌多金属矿床，褶皱期构造破碎带中形成构造蚀变岩型萨热阔布金矿床。     

Genesis of the Precambrian copper-rich Caraiba hypersthenite-norite complex,Brazil

Caraiba, the largest Brazilian copper deposit under exploitation, consists mostly of disseminated and remobilised bornite and chalcopyrite hosted in early Proterozoic norite and hypersthenite. The mafic igneous complex comprises multiple intrusions of dykes, veins and breccias of norites and hypersthenites, with minor proportions of amphibolised gabbronorite and peridotite xenoliths transported by the magma from deeper levels in the lithosphere. The country rocks are high-grade gneisses, granulites and metasediments. Compositions of plagioclase(An_60-40) and orthopyroxene(En_70-60) fall in a narrow range similar to the Koperberg Suite from the Okiep copper district, South Africa, and to that in many massif-type anorthosites. Whole-rock major and trace element geochemistry indicate a parental magma enriched in Fe, LREE, P, K, and Cu. Negative Nb anomalies on multi-element plots and fractionated REE patterns, along with sulphide sulphur isotopes in the range ³⁴S = –1.495 to + 0.643, suggest a primary mantle lithosphere source, although a lower crustal source for the gabbronorite and peridotite xenoliths cannot be excluded. Geochronological and field evidence indicate that both norite and hypersthenite are likely to have been emplaced during a major sinistral transcurrent (partly transpressional) shearing event associated with the waning stage of evolution of the early Proterozoic Salvador-Curaçá orogen.     

Geology of the High Sulfidation Copper Deposits,Monywa Mine,Myanmar

The 50 km² Monywa copper district lies near the Chindwin River within the northward continuation of the Sunda‐Andaman magmatic arc through western Myanmar. There are four deposits; Sabetaung, Sabetaung South, Kyisintaung, and the much larger Letpadaung 7 km to the southeast. Following exploration drilling which began in 1959, production of copper concentrates from a small open pit started at Sabetaung in 1983. Since 1997, when resources totaled 7 million tonnes contained copper in 2 billion tonnes ore, a heap leach–electro‐winning operation has produced over 400,000 t copper cathode from Sabetaung and Sabetaung South. Ore is hosted by mid‐Miocene andesite or dacite porphyry intrusions, and by early mid‐Miocene sandstone and overlying volcaniclastics including eruptive diatreme facies which the porphyries intrude. District‐wide rhyolite dykes and domes with marginal breccias probably post‐date andesite porphyries in the mine area and lack ore‐grade copper. Host rocks to mineralization are altered to phyllic and advanced argillic hydrothermal assemblages within an outer chlorite zone; hypogene alunite is most abundant at Letpadaung and Kyisintaung. Most mineralization is structurally‐controlled with digenite‐chalcocite in breccia dykes, in steeply dipping NE‐trending sheeted veins, and in stockwork and low‐angle sulfide veins. A high‐grade pipe at Sabetaung grades up to 30% Cu, and much of the ore at Sabetaung South is in a NE‐trending zone of mega‐breccia and stockworked sandstone. The hydrothermal alteration, together with replacement quartz, alunite and barite in breccia dykes and veins, the virtual absence of vein quartz, and the presence of chalcopyrite and bornite only as rare veins and as inclusions within the abundant pyrite, indicate that the deposits are high sulfidation. Regional uplift, resistance to erosion and leaching of the altered and mineralized rocks have resulted in porous limonite‐stained leached caps over 200 m thick forming the Letpadaung and Kyisintaung hills. The barren caps pass abruptly downwards at the water table into the highest grade ore at the top of the supergene enrichment zone, within which copper grade, supergene kaolinite and cubic alunite decrease, and pyrite increases with depth; in contrast, marcasite is mostly shallow. Much of the copper to depths exceeding 200 m below the water table occurs as supergene digenite‐chalcocite and minor covellite. Disseminated chalcocite is mostly near‐surface and hence almost certainly supergene. We infer that during prolonged uplift at all four deposits, oxidation of residual pyrite at the water table generated enough acid to leach all the copper from earlier supergene‐enriched ore; below the water table the resulting acid sulfate solutions partly replaced enargite, covellite, chalcopyrite, bornite and pyrite with supergene chalcocite. Undeformed upward‐fining cross‐bedded conglomerates and sands of the ancestral Chindwin River floodplain overlie the margins of the Sabetaung deposits, form a major aquifer up to 40 m thick, and are a potential host for exotic copper mineralization. A mid‐Miocene pluton is inferred to underlie the Monywa deposits, but the possibility of porphyry‐type mineralization within the district is at best highly speculative.