安徽铜陵冬瓜山铜矿床的叠加改造成矿机制：来自矿石结构的证据

长江中、下游地区块状硫化物矿床普遍受到燕山期岩浆及其热液的改造与叠加.本文以铜陵冬瓜山矿床为例,探讨这类矿床的成矿机制.该矿床主要由层状硫化物矿体组成,伴有矽卡岩型和斑岩型矿体.野外地质观察及室内矿相学的研究表明,冬瓜山层状矿体中矿石遭受了强烈的热变质作用及热液交代作用.进变质过程中形成的结构主要为黄铁矿受燕山期岩浆侵...     

Unique Origin of Skarn at the Ohori Base Metal Deposit,Yamagata Prefecture,NE Japan: C,O and S Isotopic Study

The Ohori ore deposit is one of the Cu–Pb–Zn deposits in the Green Tuff region, NE Japan, and consists of skarn‐type (Kaninomata) and vein‐type (Nakanomata) orebodies. The former has a unique origin because its original calcareous rocks were made by hydrothermal precipitation during Miocene submarine volcanism. Carbon and oxygen isotope ratios of skarn calcite and sulfur isotope ratios of sulfides were measured in and around the deposit. Carbon and oxygen isotope ratios of the skarn calcite are δ¹³C = ?15.51 to ?5.1‰, δ¹⁸O = +3.6 to +22.5‰. δ¹³C values are slightly lower than those of the Cretaceous skarn deposits in Japan. These isotope ratios of the Kaninomata skarn show that the original calcareous rocks resemble the present submarine hydrothermal carbonates at the CLAM Site, Okinawa Trough, than Cenozoic limestones, even though some isotopic shifts had occurred during later skarnization. δ³⁴S ratios of the sulfide minerals from the Kaninomata and Nakanomata orebodies are mostly in a narrow range of +4.0 to +7.0‰ and they resemble each other, suggesting the same sulfur origin for the both deposits. The magnetite‐series Tertiary Kaninomatasawa granite is distributed just beneath the skarn layer and has δ³⁴S ratios of +7.5 to 8.1‰. The heavy sulfur isotope ratio of the skarn sulfides may have been affected by the Kaninomatasawa granite.     

安徽铜陵冬瓜山矿床中磁黄铁矿矿石结构特征及其成因意义

安徽铜陵冬瓜山矿床是长江中下游地区具有代表性的大型层状硫化物矿床,磁黄铁矿为矿床中的主要硫化物矿物.该矿床主要由层状硫化物矿体组成,伴有矽卡岩型和斑岩型矿体.在层状矿体上部,磁黄铁矿主要为块状构造,而层状矿体下部,磁黄铁矿多为层纹状、条带状构造,具有显著的沉积结构构造特征.野外地质观察及室内矿相学研究表明,层状矿体中磁黄铁矿矿石遭受了强烈的变质作用及热液交代作用.进变质过程中形成的结构主要为胶黄铁矿转变为黄铁矿以及进一步变质转变为磁黄铁矿、磁铁矿时形成的交代残留结构.退变质过程则以磁黄铁矿的退火、黄铁矿变斑晶的生长和单纯六方磁黄铁矿的形成为特征.岩浆热液对单纯六方磁黄铁矿的交代作用形成了单斜和六方磁黄铁矿的交生结构.这些结构特征表明层状矿体中的磁黄铁矿并不是岩浆热液成因,而主要为石炭纪同生沉积胶黄铁矿、黄铁矿在燕山期岩浆侵入所引起的热变质作用下脱硫所形成,并在热变质作用之后又受到岩浆热液的叠加交代.磁黄铁矿的结构特征显示冬瓜山矿床的形成经历了同生沉积、热变质、热液交代等多个阶段,支持其为同生沉积-叠加改造型矿床.     

Erratum to: “Criteria for the detection of hydrothermal ecosystem faunas in ores of massive sulfide deposits in the Urals”

The ore-formational, ore-facies, lithological, and mineralogical-geochemical criteria are defined for the detection of hydrothermal ecosystem fauna in ores of the volcanic-hosted massive sulfide deposits in the Urals. Abundant mineralized microfauna is found mainly in massive sulfide mounds formed in the jasperous basalt (Buribai, Priorsk, Yubileinoe, Sultanov), rhyolite—basalt (Yaman-Kasy, Blyava, Komosomol’sk, Sibai, Molodezhnoe, Valentorsk), and the less common serpentinite (Dergamysh) formations of the Urals (O—D₂). In the ore-formational series of the massive sulfide deposits, probability of the detection of mineralized fauna correlates inversely with the relative abundance of felsic volcanic rocks underlying the ores. This series is also marked by a gradual disappearance of colloform pyrite, marcasite, isocubanite, pyrrhotite, and pyrite pseudomorphoses after pyrrhotite; increase of the amount of bornite, fahlores, and barite; decrease of contents of Se, Te, Co, and Sn in chalcopyrite and sphalerite; and inсrease of Tl, As, Sb, and Pb in the colloform pyrite. Probability of the detection of mineralized fauna in the morphogenetic series of massive sulfide deposits decreases from the weakly degraded sulfide mounds to the clastic stratiform deposits. The degradation degree of sulfide mounds and fauna preservation correlates with the attenuation of volcanic intensity, which is reflected in the abundance of sedimentary and volcanosedimentary rocks and the depletion of effusive rocks in the geological sections.     

Criteria for the detection of hydrothermal ecosystem faunas in ores of massive sulfide deposits in the Urals

The ore-formational, ore-facies, lithological, and mineralogical-geochemical criteria are defined for the detection of hydrothermal ecosystem fauna in ores of the volcanic-hosted massive sulfide deposits in the Urals. Abundant mineralized microfauna is found mainly in massive sulfide mounds formed in the jasperous basalt (Buribai, Priorsk, Yubileinoe, Sultanov), rhyolite–basalt (Yaman-Kasy, Blyava, Komosomol’sk, Sibai, Molodezhnoe, Valentorsk), and the less common serpentinite (Dergamysh) formations of the Urals (O–D2). In the ore-formational series of the massive sulfide deposits, probability of the detection of mineralized fauna correlates inversely with the relative abundance of felsic volcanic rocks underlying the ores. This series is also marked by a gradual disappearance of colloform pyrite, marcasite, isocubanite, pyrrhotite, and pyrite pseudomorphoses after pyrrhotite; increase of the amount of bornite, fahlores, and barite; decrease of contents of Se, Te, Co, and Sn in chalcopyrite and sphalerite; and decrease of Tl, As, Sb, and Pb in the colloform pyrite. Probability of the detection of mineralized fauna in the morphogenetic series of massive sulfide deposits decreases from the weakly degraded sulfide mounds to the clastic stratiform deposits. The degradation degree of sulfide mounds and fauna preservation correlates with the attenuation of volcanic intensity, which is reflected in the abundance of sedimentary and volcanosedimentary rocks and the depletion of effusive rocks in the geological sections.     

块状硫化物矿床的地球化学找矿标志

近年来国外发现了许多大型块状硫化物矿床，而我国进展还不大。原因之一是我们对这类矿床的地质特征，成矿条件尤其是找矿标志研究还不够。这是一类成矿物质通过热液作用在海底沉积而成的特殊矿床，故在找矿勘探讨既要研究沉积矿时形成的原生晕，又要研究热液经过围岩时蚀变而产生的次生晕?Ｍｎ晕，Ｔｌ，Ｈｇ，Ｂａ，Ａｓ和Ｚｎ等元素的异常，络合剂元素的富集，微量元素的分布，铅同位素，岩石化学异指数尤其是块状硫化物Ｃｕ矿中     

Sulfur and lead isotope geochemistry of hypogene mineralization at the Barite Hill Gold Deposit, Carolina Slate Belt, southeastern United States: a window into and through regional metamorphism

The Barite Hill gold deposit, at the southwestern end of the Carolina slate belt in the southeastern United States, is one of four gold deposits in the region that have a combined yield of 110 metric tons of gold over the past 10 years. At Barite Hill, production has dominantly come from oxidized ores. Sulfur isotope data from hypogene portions of the Barite Hill gold deposit vary systematically with pyrite–barite associations and provide insights into both the pre-metamorphic Late Proterozoic hydrothermal and the Paleozoic regional metamorphic histories of the deposit. The δ³⁴S values of massive barite cluster tightly between 25.0 and 28.0‰, which closely match the published values for Late Proterozoic seawater and thus support a seafloor hydrothermal origin. The δ³⁴S values of massive sulfide range from 1.0 to 5.3‰ and fall within the range of values observed for modern and ancient seafloor hydrothermal sulfide deposits. In contrast, δ³⁴S values for finer-grained, intergrown pyrite (5.1–6.8‰) and barite (21.0–23.9‰) are higher and lower than their massive counterparts, respectively. Calculated sulfur isotope temperatures for the latter barite–pyrite pairs (Δ=15.9–17.1‰) range from 332–355 °C and probably reflect post-depositional equilibration at greenschist-facies regional metamorphic conditions. Thus, pyrite and barite occurring separately from one another provide pre-metamorphic information about the hydrothermal origin of the deposit, whereas pyrite and barite occurring together equilibrated to record the metamorphic conditions. Preliminary fluid inclusion data from sphalerite are consistent with a modified seawater source for the mineralizing fluids, but data from quartz and barite may reflect later metamorphic and (or) more recent meteoric water input. Lead isotope values from pyrites range for ²⁰⁶Pb/²⁰⁴Pb from 18.005–18.294, for ²⁰⁷Pb/²⁰⁴Pb from 15.567–15.645, and for ²⁰⁸Pb/²⁰⁴Pb from 37.555–38.015. The data indicate derivation of the ore leads from the country rocks, which themselves show evidence for contributions from relatively unradiogenic, mantle-like lead, and more evolved or crustal lead. Geological relationships, and stable and radiogenic isotopic data, suggest that the Barite Hill gold deposit formed on the Late Proterozoic seafloor through exhalative hydrothermal processes similar to those that were responsible for the massive sulfide deposits of the Kuroko district, Japan. On the basis of similarities with other gold-rich massive sulfide deposits and modern seafloor hydrothermal systems, the gold at Barite Hill was probably introduced as an integral part of the formation of the massive sulfide deposit. Received: 17 August 1998 / Accepted: 12 October 2000     

Isotopes and Geochronology of the Meixian-type Pb-Zn-(Ag)Deposits,Central Fujian Rift,South China:Implications for Geological Events

Central Fujian Rift is another new and important volcanogenic massive sulfide Pb-Zn polymetallic metallogenetic belt. In order to find out the material genesis and mineralization period of Meixian-type Pb-Zn-Ag deposits, S and Pb isotope analysis and isotope geochronology of ores and wall rocks for five major deposits are discussed. It is concluded that the composition of sulfur isotope from sulfide ore vary slightly in different deposits and the mean value is close to zero with the 834S ranging from -3.5‰ to ＋5.6‰ averaging at ＋2.0‰, which indicates that the sulfur might originate from magma or possibly erupted directly from volcano or was leached from ore-hosted volcanic rock. The lead from ores in most deposits displays radioactive genesis character （206pb/204pb〉18.140, 207Pb/204pb〉15.584, 208pb/204pb〉38.569） and lead isotope values of ores are higher than those of wall rocks, which indicates that the lead was likely leached from the ore-hosted volcanic rocks. Based on isotope data, two significant Pb-Zn metallogenesis are delineated, which are Mid- and Late-Proterozoic sedimentary exhalative metailogenesis （The single zircon U-Pb, Sm-Nd isochronal and Ar-Ar dating ages of ore- hosted wall rocks are calculated to be among 933-1788 Ma.） and Yanshanian magmatic hydrothermal superimposed and alternated metallogenesis （intrusive SHRIMP zircon U-Pb and Rb-Sr isochronal ages between 127-154 Ma）.     

Geology and Geochemistry of the Buerkesidai and Kuoerzhenkuola Gold Deposits in the Sawuershan Region, Xinjiang Uigur Autonomous Region, Northwest China

The Sawuershan region, one of the important gold metallogenic belts of Xinjiang, is located in the western part of the Kalatongke island arc zone of north Xinjiang, NW China. There are two gold deposits in mining, namely the Kuoerzhenkuola and the Buerkesidai deposits. Gold ores at the Kuoerzhenkuola deposit occur within Carboniferous andesite and volcanic breccias in the form of gold‐bearing quartz–pyrite veins and veinlet groups containing native gold, electrum, pyrite, pyrrhotite and chalcopyrite. Gold ores at the Buerkesidai deposit occur within Carboniferous tuffaceous siltstones in the form of gold‐bearing quartz veinlet groups and altered rocks, with electrum, pyrite and arsenopyrite as major metallic minerals. Both gold deposits are hosted by structurally controlled faults associated with intense hydrothermal alteration. The typical alteration assemblage is sericite + chlorite + calcite + quartz, with an inner pyrite–sericite zone and an outer chlorite–calcite–epidote zone between orebodies and wall rocks. δ³⁴S values (0.3–1.3‰) of pyrite of ores from Kuoerzhenkuola deposit are similar to those (0.4–2.9‰) of pyrite of ores from Buerkesidai deposit. δ³⁴S values (1.1–2.8‰) of pyrite from altered rocks are similar to δ³⁴S values of magmatic or igneous sulfide sulfur, but higher than those from ores. ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb data of sulfide from ores range within 17.72–18.56, 15.34–15.61, and 37.21–38.28, respectively. These sulfur and lead isotope compositions imply that ore‐forming materials might originate from multiple, mainly deep sources. He and Ar isotope study on fluid inclusions of pyrites from ores of Kuoerzhenkuola and Buerkesidai gold deposits produces ⁴⁰Ar/³⁶Ar and ³He/⁴He ratios in the range of 282–525 and 0.6–9.4 R/Ra, respectively, indicating a mixed source of deep‐seated magmatic water (mantle fluid) and shallower meteoric water. In terms of tectonic setting, the gold deposits in the Sawuershan region can be interpreted as epithermal. These formations resulted from a combination of protracted volcanic activity, hydrothermal fluid mixing, and a structural setting favoring gold deposition. Fluid mixing was possibly the key factor resulting in Au deposition in the gold deposits in Sawuershan region.     

The source of sulfur in sulfide deposits in the Siberian Platform traps (from isotope data)

The source of sulfur in giant Norilsk-type sulfide deposits is discussed. A review of the state of the problem and a critical analysis of existing hypotheses are made. The distribution of δ³⁴S in sulfides of ore occurrences and small and large deposits and in normal sedimentary, metamorphogenic, and hypogene sulfates is considered. A large number of new δ³⁴S data for sulfides and sulfates in various deposits, volcanic and terrigenous rocks, coals, graphites, and metasomatites are presented. The main attention is focused on the objects of the Norilsk and Kureika ore districts. The δ³⁴S value varies from -14 to + 22.5‰ in sulfides of rocks and ores and from 15.3 to 33‰ in anhydrites. In sulfide-sulfate intergrowths and assemblages, δ³⁴S is within 4.2-14.6‰ in sulfides and within 15.3-21.3‰ in anhydrites. The most isotopically heavy sulfur was found in pyrrhotite veins in basalts (δ³⁴S = 21.6‰), in sulfate veins cutting dolomites (δ³⁴S = 33‰), and in subsidence caldera sulfates in basalts (δ³⁴S = 23.2-25.2‰). Sulfide ores of the Tsentral’naya Shilki intrusion have a heavy sulfur isotope composition (δ³⁴S = + 17.7‰ (n = 15)). Thermobarogeochemical studies of anhydrites have revealed inclusions of different types with homogenization temperatures ranging from 685 °C to 80 °C. Metamorphogenic and hypogene anhydrites are associated with a carbonaceous substance, and hypogene anhydrites have inclusions of chloride-containing salt melts. We assume that sulfur in the trap sulfide deposits was introduced with sulfates of sedimentary rocks (δ³⁴S = 22-24‰). No assimilation of sulfates by basaltic melt took place. The sedimentary anhydrites were “steamed” by hydrocarbons, which led to sulfate reduction and δ³⁴S fractionation. As a result, isotopically light sulfur accumulated in sulfides and hydrogen sulfide, isotopically heavy sulfur was removed by aqueous calcium sulfate solution, and “residual” metamorphogenic anhydrite acquired a lighter sulfur isotope composition as compared with the sedimentary one. The wide variations in δ³⁴S in sulfides and sulfates are due to changes in the physicochemical parameters of the ore-forming system (first of all, temperature and P_ch4) during the sulfate reduction. The regional hydrocarbon resources were sufficient for large-scale ore formation.     

Hydrothermal mineralization at seafloor spreading centers

The recent recognition that metallic mineral deposits are concentrated by hydrothermal processes at seafloor spreading centers constitutes a scientific breakthrough that opens active sites at seafloor spreading centers as natural laboratories to investigate ore-forming processes of such economically useful deposits as massive sulfides in volcanogenic rocks on land, and that enhances the metallic mineral potential of oceanic crust covering two-thirds of the Earth both beneath ocean basins and exposed on land in ophiolite belts. This paper reviews our knowledge of processes of hydrothermal mineralization and the occurrence and distribution of hydrothermal mineral deposits at the global oceanic ridge-rift system.Sub-seafloor hydrothermal convection involving circulation of seawater through fractured rocks of oceanic crust driven by heat supplied by generation of new lithosphere is nearly ubiquitous at seafloor spreading centers. However, ore-forming hydrothermal systems are extremely localized where conditions of anomalously high thermal gradients and permeability increase hydrothermal activity from the ubiquitous low-intensity background level (? 200°C) to high-intensity characterized by high temperatures ( > 200–c.400°C), and a rate and volume of flow sufficient to sustain chemical reactions that produce acid, reducing, metal-rich primary hydrothermal solutions. A series of mineral phases with sulfides and oxides as high- and low-temperature end members, respectively, are precipitated along the upwelling limb and in the discharge zone of single-phase systems as a function of increasing admixture of normal seawater.The occurrence of hydrothermal mineral deposits is considered in terms of spatial and temporal frames of reference. Spatial frames of reference comprise structural features along-axis (linear sections that are the loci of seafloor spreading alternating with transform faults) and perpendicular to axis (axial zone of volcanic extrusion and marginal zones of active extension) common to all spreading centers, regional tectonic setting determined by stage (early, advanced), and rate (slow, intermediate-to-fast) of opening of an ocean basin about a spreading center, and local tectonic sub-setting that incorporates anomalous structural and thermal conditions conducive to mineral concentration (thermal gradient, permeability, system geometry, leaky versus tight hydrothermal systems). Temporal frames of reference comprise the relation between mineral concentration and timing of regional plutonic, volcanic and tectonic cycles and of episodic local physical and chemical events (transient stress, fluctuating heat transfer, intrusion-extrusion, fracturing, sealing, etc.). Types of hydrothermal deposits are not uniquely associated with specific tectonic settings and subsettings. Similar types of hydrothermal deposits may occur in different tectonic settings as a consequence of convergence of physical and chemical processes of concentration.Local tectonic sub-settings with conditions conducive to hydrothermal mineralization at slow-spreading centers (half rate ≤ 2cm y^?1; length c. 28,000 km), characterized by an estimated average convective heat transfer of 15.1·10⁸ cal. cm^?2, deep-level ( > 3 km), relative narrow (< 5 km wide at base) magma chambers, and high topographic relief (1–5 km) are: (1) basins along linear sections of the axial zone of volcanic extrusion near transform faults at an early stage of opening, represented by a large stratiform sulfide deposit (estimated 32.5·10⁶ metric tons) of the Atlantis II Deep of the Red Sea; (2) the wall along linear sections of the rift valley in the marginal zone of active extension at an advanced stage of opening, represented by encrustations and layered deposits of manganese and iron oxides, hydroxides and silicates inferred to be underlain by stockwork sulfides at the TAG Hydrothermal Field at latitude 26°C on the Mid-Atlantic Ridge; (3) transform faults, especially those with large ridge-ridge offset ( > 30 km), at an advanced stage of opening, represented by stockwork sulfides exposed in the walls of equatorial fracture zones of the Atlantic Ocean and Indian Ocean; (4) the axial zone of volcanic extrusion at an advanced stage of opening.Local tectonic sub-settings with conditions conducive to hydrothermal mineralization at intermediate- to fast-spreading centers (half rate > 2cm y^?1; length c. 22,000 km) characterized by an estimated average convective heat transfer of 11.5·10⁸ cal. cm^?2, relatively wide (up to 20 km at base), shallow-level (c. 1–3 km) magma chambers, and low topographic relief (< 1 km), are: (1) basins along linear sections of the axial zone of volcanic extrusion at an early stage of opening, represented by massive sulfide deposits of the Guaymas Basin of the Gulf of California; (2) the axial zone of volcanic extrusion at an advanced stage of opening, represented by individually small (c. 1·10³ metric tons), massive sulfide mounds surmounted by chimneys of the East Pacific Rise at latitude 21°N; (3) the marginal zone of active extension at an advanced stage of opening represented by a large, massive sulfide deposit (preliminary tentative estimate c.10·10⁶ metric tons) at a double-rifted section of the Galapagos Spreading Center; (4) transform faults, especially those with large ridge-ridge offset ( > 50 km) represented by manganese encrustations in a transform fault at the Galapagos Spreading Center; (5) volcanic seamounts related to persistent hot spots at spreading centers, represented by oxide and sulfide deposits on seamounts off the axis of the East Pacific Rise; (6) portions of spreading centers with anomalous configurations such as multiple, bent or extended rifts, represented by massive sulfide deposits at a double-rifted section of the Galapagos Spreading Center, suggesting the operation of a thermal-structural feedback mechanism indicative of the presence of hydrothermal mineralization; (7) discrete spreading centers in back-arc basins represented by hydrothermal deposits at sites in marginal seas of the western Pacific.Ore-forming processes appear to be least efficient in the axial zone of volcanic extrusion of oceanic ridges at an advanced stage of opening irrespective of spreading rate, where tight hydrothermal systems dissipate a major portion of contained metals by precipitation and dispersion in particulate form from “black smokers” that discharge into the water column. Ore-forming processes appear to be most efficient at sites in basins at linear sections of the axial zone of volcanic extrusion near transform faults during an early stage of opening, and at marginal zones of active extension along linear sections of a spreading center during an advanced stage of opening, irrespective of spreading rate, where both tight and leaky hydrothermal systems may conserve their contained metals to concentrate large sulfide deposits. Resemblances in mineralization between stockwork sulfides at seafloor spreading centers and porphyry copper-type deposits in volcanogenic rocks on land suggest the possibility for the occurrence of large tonnage, low-grade porphyry copper-like deposits concentrated by leaky hydrothermal systems at spreading centers. Systematic application of composite exploration procedures is leading to the discovery of numerous additional deposits. It is inferred from the limited data base available that the occurrence of hydrothermal mineral deposits is more frequent at intermediate-to-fast-than at slow-spreading centers, but the potential for the accumulation of large hydrothermal mineral deposits is greater at slow-spreading centers.Current knowledge of the distribution of hydrothermal mineral deposits at seafloor spreading centers is limited to about 55 sites at this early stage of exploration. Estimates of the distribution of either fields of hydrothermal mineral deposits or high-intensity ore-forming hydrothermal systems at seafloor spreading centers, deduced from various considerations, range from one such occurrence between 15 and 265 km along slow-spreading centers, and 1 and 100 km along intermediate- to fast-spreading centers. However, the distribution of sizable deposits will remain sporadic owing to the special structural and thermal conditions necessary to sustain and to retain high-intensity ore-forming hydrothermal systems.     

Aperçu sur les amas sulfurés massifs des hercynides Marocaines

Massive sulfide deposits located on Hercynian islets of northwestern Morocco exhibit four main characteristics:

They are strata-bound massive pyrrhotite deposits mined for sulfur and/or base metals occasionally occurring as sulfides of workable grade.

Volcanic rocks with which these massive sulfide orebodies are associated are scarce, although always present as acid flows of submarine emissions of either rhyolitic or more often quartz-keratophyric nature. Later on, basic plutonics intruded the pelitic country rocks.

Stockworks underlying the massive sulfide orebodies are common, but not systematic. When present, they occur in siltite ± phyllite ± carbonate rocks at the wall of massive sulfide lenses. They consist of fissural disseminations transformed by epimetamorphic recrystallization and by one schistosity generally concordant with s₀.

Associated alterites and exhalites belong to three types, i.e., sericitite (or biotite-rich rock), chloritite, and/or chert (jasper).

Generally well located in a back-arc basin environment characterized by a two-phase geological history, i.e., “extension and volcanism, compression and metamorphism”, these volcano-sedimentary deposits exhibit distal features with regard to the volcanism coeval with their sedimentation. They are mostly linked with strongly reducing environmental properties entailing pyrrhotite and/or magnetite syngenetic deposition, whatever the iron activity.     

Geological and Geochemical Characteristics of the Huangshilao Stratabound Gold Deposit in the Tongguanshan Orefield,Tongling, East‐Central China

The Huangshilao gold deposit (>13.5 t Au) is comprised of stratabound pyrite‐dominant massive sulfide ores, and is distinguished from the skarn Cu, Au, and Cu–Au deposits that are dominant in the Tongguanshan orefield, Tongling, east‐central China. The stratabound orebodies are situated along flexural slip faults along the unconformity between the Upper Devonian Wutong and the Upper Carboniferous Huanglong Formations. The ores, dominated by crystallized pyrite, colloform pyrite, and pyrrhotite, are systematically sampled from the underground stopes along strike drifts. The δ³⁴S values of ore sulfides yield a wide variation from ?11.3 to 11.4‰, but mostly within 4–8‰, corresponding to the δ³⁴S range (3.4–8.7‰) of the Yanshanian Tongguanshan and Tianshan quartz diorite intrusions in the Tongguanshan orefield, suggesting a magmatic dominated sulfur source. Few obvious negative δ³⁴S values are induced by an involvement of sedimentation‐related biogenic sulfur. The wide δ³⁴S variation denotes an incongruent physical and chemical interaction of the two sources. Combined analysis of gold contents and sulfur isotopes of the sulfides show that the magmatic hydrothermal solution provides primary metals despite a small quantity that may have been contributed by the sedimentary pyrites. The hydrothermal alteration, thermal metamorphism, trace element concentration in pyrites, and existing aeromagnetic data jointly suggest that the hydrothermal fluid migrated vertically from an intrusion below, along the flexural slip faults, but not laterally from the nearby outcrop of Tianshan stock.     

Boron,sulphur and copper isotope systematics in the orogenic gold deposits of the Archaean Hattu schist belt,eastern Finland

The Hattu schist belt is located in the western part of the Archaean Karelian domain of the Fennoscandian Shield. The orogenic gold deposits with Au–Bi–Te geochemical signatures are hosted by NE–SW, N–S and NW–SE oriented shear zones that deform 2.76–2.73 Ga volcanic and sedimentary sequences, as well as 2.75–2.72 Ga tonalite–granodiorite intrusions and diverse felsic porphyry dykes. Mo–W mineralization is also present in some tonalite intrusions, both separate from, and associated with Au mineralization. Somewhat younger, unmineralized leucogranite intrusions (2.70 Ga) also intrude the belt. Lower amphibolite facies peak metamorphism at 3–5 kbar pressures and at 500–600 °C temperatures affected the belt at around 2.70 Ga and post-date hydrothermal alteration and ore formation. In this study, we investigated the potential influence of magmatic-hydrothermal processes on the formation of orogenic gold deposits on the basis of multiple stable isotope (B, S, Cu) studies of tourmaline and sulphide minerals by application of in situ SIMS and LA ICP MS analytical techniques.Crystal chemistry of tourmaline from a Mo–W mineralization hosted by a tonalite intrusion in the Hattu schist belt is characterized by Fe^3 +–Al^3 +-substitution indicating relatively oxidizing conditions of hydrothermal processes. The range of δ¹¹B data for this kind of tourmaline is from − 17.2‰ to − 12.2‰. The hydrothermal tourmaline from felsic porphyry dyke swith gold mineralization has similar crystal chemistry (e.g. dravite–povondraite compositional trend with Fe^3 +–Al^3 + substitution) and δ¹¹B values between − 19.0‰ and − 9.6‰. The uvite–foitite compositional trend and δ¹¹B ‰ values between − 24.1% and − 13.6% characterize metasomatic–hydrothermal tourmaline from the metasediment-hosted gold deposits. Composition of hydrothermal vein-filling and disseminated tourmaline from the gold-bearing shear zones in metavolcanic rocks is transitional between the felsic intrusion and metasedimentary rock hosted hydrothermal tourmaline but the range of average boron isotope data is essentially identical with that of the metasediment-hosted tourmaline. Rock-forming (magmatic) tourmaline from leucogranite has δ¹¹B values between − 14.5‰ and − 10.8‰ and the major element composition is similar to that of the metasediment-hosted tourmaline.The range of δ³⁴S_VCDT values measured in pyrite, chalcopyrite and pyrrhotite is from − 9.1 to + 8.5‰, which falls within the typical range of sulphur isotope data for Archaean orogenic gold deposits. In the Hattu schist belt, positive δ³⁴S_VCDT values characterize metasediment-hosted gold ores with sulphide parageneses dominated by pyrrhotite and arsenopyrite. The δ³⁴S_VCDT values are both positive and negative in ore mineral parageneses within felsic intrusive rocks in which variable amounts of pyrrhotite are associated with pyrite. Purely negative values were only recorded from the pyrite-dominated gold mineralization within metavolcanic units. Therefore the shift of δ³⁴S_VCDT values to the negative values reflects precipitation of sulphide minerals from relatively oxidizing fluids. The range of measured δ⁶⁵Cu_NBS978 values from chalcopyrite is from − 1.11 to 1.19‰. Positive values are common for mineralization in felsic intrusive rocks and negative values are more typical for deposits confined to metasedimentary rocks. Positive and negative δ⁶⁵Cu_NBS978 values occur in the ores hosted by metavolcanic rocks. There is no correlation between sulphur and copper isotope data obtained in the same chalcopyrite grains.Evaluation of sulphur and boron isotope data together and comparisons with other Archaean orogenic gold provinces supports the hypothesis that the metasedimentary rocks were the major sources of sulphur and boron in the orogenic gold deposits in the Hattu schist belt. Variations in major element and boron isotope compositions in tourmaline, as well as in the δ³⁴S_VCDT values in sulphide minerals are attributed to localized involvement of magmatic fluids in the hydrothermal processes. The results of copper isotope studies indicate that local sources of copper in orogenic gold deposits may potentially be recognized if the original, distinct signatures of the sources have not been homogenized by widespread interaction of fluids with a large variety of rocks and provided that local chemical variations have been too small to trigger changes in the oxidation state of copper during hydrothermal processes.     

A magmatic source of hydrothermal sulfur for the Prominent Hill deposit and associated prospects in the Olympic iron oxide copper-gold (IOCG) province of South Australia

The Prominent Hill deposit is a world-class iron oxide copper–gold (IOCG) deposit in South Australia, characterized by a high Cu/S ratio of the dominant Cu-(Fe) sulfides hosted by hematite breccias. It contains a total resource of 278 Mt of ore at 0.98% Cu and 0.75 g/t Au. Prominent Hill is one of several IOCG deposits and numerous prospects in the Olympic IOCG province that are temporally associated with the 1603–1575 Ma Gawler Range Volcanics, a large igneous province including co-magmatic granitoid intrusions of the Hiltaba Suite. Globally, IOCG deposits share many similar features in terms of their geological environment and mineral association. However, it is not yet clear whether sulfur and copper originate from the same source rocks and which hydrothermal redox processes created the characteristic iron oxide enrichment. Highly variable sulfur isotope compositions of sulfides and sulfates in IOCG deposits have previously been interpreted in terms of diverse sulfur sources that may include contributions from magmatic, sedimentary, seawater or evaporitic sulfur. In order to test these alternatives, we performed a detailed sulfur isotope study of Cu-(Fe) sulfides from Prominent Hill and IOCG prospects nearby. The Prominent Hill deposit shows a wide range in δ³⁴S_V-CDT between − 33.5‰ and 29.9‰ for Cu-(Fe) sulfides, and a narrower range of 4.3‰ to 15.8‰ for barite. Iron sulfides (pyrite, pyrrhotite) show a narrow range in sulfur isotope composition, whereas Cu-bearing sulfides show a much wider range, and more negative δ³⁴S_V-CDT values on average. We propose a two-stage sulfide mineralization model for the IOCG system in the Prominent Hill area, in which all hydrothermal sulfur is ultimately derived from a magmatic source that had a composition of 4.4 ± 2‰. The diversity in sulfur isotope composition can be produced by different fluid evolution pathways along reducing or oxidizing trajectories. A reduced sulfur evolution pathway is responsible for stage I mineralization, when intrusion-derived magmatic-hydrothermal fluids produced early pyrite and minor chalcopyrite at Prominent Hill, and iron ± copper sulfides in regional magnetite skarns and in some pervasively altered volcanic rocks of the Gawler Range Volcanics. Shallow-venting magmatic-hydrothermal fluids and subaerial volcanic gases that became completely oxidized by reaction with atmospheric oxygen produced sulfate and sulfuric acid with a sulfur isotope composition equal to their magmatic source. This highly oxidized ore fluid probably consisted dominantly of water from the hydrosphere, but contained magmatic solute components, notably sulfate, acidity and Cu. Sulfate reduction produced hydrothermal Cu sulfides with a wide range in sulfur isotope compositions from very negative to moderately positive values. Partial reaction of the Cu-rich stage II fluid with earlier stage I sulfides resulted in mixing of sulfur derived from sulfate reduction and from sulfides deposited during stage I. Modeling of the sulfur isotope fractionation processes in response to reducing and oxidizing pathways demonstrates that the entire spectrum of sulfur isotope data from stage I and stage II mineralization can be explained with a single, ultimately magmatic sulfur source. Such a magmatic sulfur source is also adequate to explain the complete spectrum of sulfur isotope data of other IOCG prospects and deposits in the Olympic province, including Olympic Dam. The results of our study challenge the conventional model that suggests the requirement of multiple and compositionally diverse sulfur sources in hematite-breccia hosted IOCG style mineralization.     

Seawater contribution to polymetallic Ni–Mo–PGE–Au mineralization in Early Cambrian black shales of South China: Evidence from Mo isotope,PGE, trace element,and REE geochemistry

The Early Cambrian black shale sequence of the Niutitang Formation in South China hosts a synsedimentary, organic carbon-rich, polymetallic sulfide layer with extreme metal concentrations, locally mined as polymetallic Ni–Mo–PGE–Au ore. In combination with previously reported data, we present Mo isotope, platinum-group element (PGE), and trace and rare-earth element (REE) data for the polymetallic sulfide ores and host black shales from four mine sites (Dazhuliushui and Maluhe in Guizhou Province, and Sancha and Cili in Hunan Province, respectively), several hundred kilometers apart. The polymetallic sulfide ores have consistently heavy δ^98/95Mo values of 0.94 to 1.38‰ (avg. 1.13 ± 0.14‰, 1σ, n = 11), and the host black shale and phosphorite have slightly more variable δ^98/95Mo values of 0.81‰ to 1.70‰ (n = 14). This latter variation is due to variable paleoenvironmental conditions from suboxic to euxinic, and partly closed-system fractionation in isolated marine sedimentary basins. Both the polymetallic sulfides and host black shales show PGE distribution patterns similar to that of present-day seawater, but different from those of ancient submarine-hydrothermal deposits and modern submarine hydrothermal fluids. The polymetallic sulfide bed has a generally consistent metal enrichment by a factor of 10⁷ compared to present-day seawater. PAAS-normalized REE + Y patterns of the polymetallic sulfide bed are characterized by a remarkably positive Y anomaly, consistent with an origin of the REE predominantly from seawater. Small positive Eu anomalies in some of the sulfide ores could reflect minor hydrothermal components involved. The Mo isotope, PGE, and trace and rare-earth element geochemical data suggest that metals in the polymetallic Ni–Mo–PGE–Au sulfide ore layer were scavenged mostly from Early Cambrian seawater, by both in-situ precipitation and local re-deposition of sulfide clasts.     

Mineralogical and sulfur isotopic characteristics of Archean greenstone belt-hosted gold mineralization at the Tau deposit of the Mupane gold mine,Botswana

The Mupane gold deposit, which is one of the numerous gold occurrences in the Tati Greenstone Belt in the northeastern part of Botswana, consists of four orebodies, namely Tau, Tawana, Kwena, and Tholo deposits. The present research, which focuses on the genesis of the Tau deposit, was based on ore petrography, mineral chemistry of sulfides, and sulfur isotope data. Mineralogical characteristics of the host rocks indicate that banded iron formation at the Tau deposit includes iron oxides (magnetite), carbonates (siderite and ankerite), silicates (chlorite and amphibole), and sulfides (arsenopyrite and pyrrhotite). The deposit features arsenopyrite-rich zones associated with biotite-chlorite veins, which are indicative of the precipitation of arsenopyrite concomitant with potassic alteration. The replacement of magnetite by pyrrhotite in some samples suggests that sulfidation was likely the dominant gold precipitation mechanism because it is considered to have destabilized gold-thiocomplexes in the ore-forming fluids. Based on textural relationships and chemical composition, arsenopyrite is interpreted to reflect two generations. Arsenopyrite 1 is possibly early in origin, sieve textured with abundant inclusions of pyrrhotite. Arsenopyrite 1 was then overgrown by late arsenopyrite 2 with no porous textures and rare inclusions of pyrrhotite. Gold mineralization was initiated by focused fluid flow and sulfidation of the oxide facies banded iron formation, leading to an epigenetic gold mineralization. The mineralogical assemblages, textures, and mineral chemistry data at the Tau gold deposit revealed two-stage gold mineralizations commencing with the deposition of invisible gold in arsenopyrite 1 followed by the later formation of native gold during hydrothermal alteration and post-depositional recrystallization of arsenopyrite 1. Laser ablation inductively coupled plasma mass spectrometric analysis of arsenopyrite from the Tau deposit revealed that the hydrothermal event responsible for the formation of late native gold also affected the distribution of other trace elements within the grains as evidenced by varying trace elements contents in arsenopyrite 1 and arsenopyrite 2. The range of δ³⁴S of gold-bearing assemblages from the Tau deposit is restricted from +1.6 to +3.9‰, which is typical of Archean orogenic gold deposits and indicates that overall reduced hydrothermal conditions prevailed during the gold mineralization process at the Tau deposit. The results from this study suggest that gold mineralization involved multi-processes such as sulfidation, metamorphism, deformation, hydrothermal alteration, and gold remobilization.     

还原性斑岩型Cu与Mo-Cu矿特征与形成机制

还原性斑岩型Cu矿是近年新识别的一类斑岩型矿床,以岩浆阶段发育大量磁黄铁矿和成矿流体富CH4为主要特征。成因上,还原性斑岩型Cu矿与钛铁矿系列I型花岗岩伴生,形成于俯冲环境或者后碰撞环境。成矿流体为岩浆流体。岩浆阶段磁黄铁矿的结晶沉淀将导致岩浆中成矿元素Cu进入硫化物相而贫化,不利于成矿元素在流体中富集,结果导致还原性斑岩型Cu矿的矿化和蚀变规模较小。对比研究发现西准噶尔宏远Mo-Cu矿也具有还原性斑岩型矿床的特征,可能为还原性斑岩型矿床的新类型。     

现代海底热液成矿作用研究现状及发展方向

现代海底热水成矿作用研究的重大进展表现在两个方面：（１）大批活动的和窒息的热液活动区和硫化物矿床在洋脊、岛弧、弧后盆地及板内火山活动中心等海底环境相继发现。在沉积物饥饿洋脊，矿床规模较小，Ｃｕ－Ｚｎ为主，沉积物覆盖洋脊，矿床规模巨大，Ｐｂ－Ｚｎ为主。弧后扩张或弧间裂陷盆地，形成Ｐｂ－Ｚｎ→Ｚｎ－Ｐｂ－Ｃｕ→Ｃｕ－Ｚｎ矿床谱系。岛弧环境硫化物矿床不具规模，板内火山活动中心以氧化物－硫化物矿化为特色。（２）现代海底热水成矿作用观察和研究为古代ＶＭＳ矿床成因研究提供了重要信息，对现有成矿理论产生重要影响。现代成矿观念强调：①海底成矿作用虽可产生于不同环境，但均与张裂断陷事件密切相关。矿床规模和分布特点受张裂速率制约；②成矿物质主体来源于热水循环的火山－沉积岩和下伏基底物质；③硫化物堆积发生于丘堤－烟囱联合构成的机构和结壳下部，通过开放空间的硫化物充填和先成矿石淋滤迁移来实现。④热液流体呈双扩散对流循环。现代海底热水成矿作用的未来研究方向可概括为强度方向和广度方向。广度研究将加大力度去发现新的矿床，强度研究将采用地球物理方法并配以必要的钻探，深入揭示矿床的三维结构和热液体系及成矿机制。     

Genetic Aspects of the Manto-type Copper Deposits Based on Geochemical Studies of North Chilean Deposits

Recent studies on mineralogy, geochronology, fluid inclusion and stable isotope (Pb, Os, S, C, O, Sr) characteristics were reviewed to determine constraints for genetic models of the Chilean manto‐type copper deposits. The Chilean manto‐type deposits are divided into the two geologic categories of the northern areas (Arica–Iquique, Tocopilla–Taltal) and the central areas (Copiapó, La Serena, Santiago). The former is distributed in the coastal range composed of Jurassic andesite‐dominated volcano‐sedimentary piles and younger plutonic intrusions, and yields chalcocite (‐digenite) and bornite as the principal hypogene copper sulfides. The latter is hosted mostly in Lower Cretaceous volcano‐sedimentary sequences, and has chalcopyrite‐rich mineral associations. The fluid inclusion data indicate that the primary copper mineralization was commonly generated in the temperature range 150–360°C under low‐pressure conditions near the boiling curve, mediated with relatively saline brines. Generally, homogeneous Pb and S isotope compositions for primary copper minerals imply direct magma source or leaching of igneous rocks. Pb and Os isotope data published for some deposits, however, suggest that ore‐forming metals were derived mainly from the volcano‐sedimentary host rocks. The noticeably negative isotope ratios of primary sulfide sulfur and hydrothermal calcite carbon of some central area deposits indicate influx of sedimentary rock components, and the high ⁸⁷Sr/⁸⁶Sr initial ratios of hydrothermal calcite from the Tocopilla–Taltal area deposits imply contribution of the contemporaneous seawater or marine carbonates. These isotopic constraints imply a formation mechanism in which the Chilean manto‐type copper deposits formed epigenetically in the process of hydrothermal interaction of non‐magmatic surface‐derived brine with the volcano‐sedimentary host rocks, which is inferred to have been induced by a deep‐seated plutonic complex as the possible heat source.