福建上杭紫金山高硫化型铜矿床矿化分带特征

通过矿相学,系统分析铜硫化物以及脉石矿物的结构构造、形态特征以及嵌布特征,主要铜硫化物为铜蓝、斜方蓝辉铜矿;通过电子探针,分析铜硫化物各种元素含量,尤其是主量元素Cu/S比值垂向变化规律在钻孔浅部无明显规律,随着深度增加Cu/S比值逐渐减小,最后趋近于一个常数约为1.3。铜矿成矿影响因素:(1)火山机构的温度影响范围有限,并未改变铜硫化物的矿物组合特征,只是影响铜硫化物Cu/S比值分配,表现为越远离火山机构Cu/S比值越高;(2)高氧逸度条件是形成稳定铜硫化物的重要条件。氧逸度垂向由上至下先是具有高氧逸度,随着深度增加氧逸度逐渐减小,最后增加为高氧逸度。Cu/S比值变化规律为今后紫金山铜矿深部找矿提供重要的矿化信息。     

Lead isotopes in sulfides from the Stillwater Complex, Montana: evidence for subsolidus remobilization

Isotopic ratios of Pb in sulfide minerals (primarily pyrrhotite, chalcopyrite, and pentlandite) from a suite of samples from the platiniferous J-M Reef of the Stillwater Complex were measured to elucidate the temporal and genetic relationship between sulfides and host silicate minerals. Results indicate that sulfides and coexisting plagioclases are generally not in isotopic equilibrium, that both sulfides and feldspars record highly radiogenic initial ratios at 2.7 Ga, and that a component of “post-emplacement” radiogenic Pb has mixed with common Pb in the sulfides. A model involving introduction of radiogenic Pb carried by fluids derived from sources external to the complex is favored. Analyses of the lead isotopic composition of sulfides in veins which cut the complex indicate that a significant fraction of the radiogenic lead which was added to the sulfides was externally derived during an extensive hydrothermal episode, associated with Proterozoic regional metamorphism around 1.7 Ga. The possibility that some fractions of the radiogenic Pb may have been derived from primary minerals altered during the low-grade metamorphism cannot be discounted. The amount of radiogenic lead added is variable and in some cases negligible. There is a good correlation between the lead isotope composition and the nature of the secondary mineral assemblage. Sulfides and plagioclases in samples that show little or no alteration of the primary minerals are generally in isotopic equilibrium and preserve isotope ratios consistent with magmatic crystallization at 2.7 Ga. Samples with the most radiogenic sulfides contain abundant secondary minerals (serpentine, talc, actinolite, chlorite and zoisite) associated with greenschist facies metamorphism. Some of the radiogenic Pb in the sulfides can be removed by progressive stepwise leaching. However, in most samples recrystallization of sulfides during metamorphism has mixed common Pb and radiogenic Pb throughout the crystal structure such that, in these samples, stepwise leaching does not recover initial Pb isotopic ratios. Plagioclases are much more resistant to low temperature recrystallization and in almost all cases, stepwise leaching reveals the initial lead isotopic composition. The reactivity of sulfides over a wide temperature range enhances their utility in understanding not only the processes involved in their formation at the time of magmatic emplacement but also postmagmatic processes which were important in the redistribution and enrichment of platinum group elements (PGE) within the ore zone. Received: 30 December 1998 / Accepted: 16 June 1999     

Sulfur isotope study of a modern intertidal environment,and the interpretation of ancient sulfides

Extensive sulfur isotope distribution data for sulfides precipitated in an intertidal environment show no distinctive features when compared with isotope values for other marine, sedimentary sulfides. The fractionation ranges from α = 1.030 to α = 1.048. The pattern is characteristic for a system essentially open to sulfate, and isotope analyses of interstitial sulfates are corroborative. A population of sulfate-reducing bacteria of the order of 10⁹ organisms per cc of interstitial water is indicated. Seasonal variation of the isotope distribution reflects a transient sulfide composition and a bacterial population in which the fractionation effect is indirectly controlled by temperature. The data presented for this modern shallow water environment are at variance with an earlier assessment of isotopic distributions in ancient sulfides which linked shallow water environments with limited fractionation (α ? 1.025) in a closed system.     

Sulfide evolution in high-temperature to ultrahigh-temperature metamorphic rocks from Lützow–Holm Complex, East Antarctica

The high-temperature (HT) to ultrahigh-temperature (UHT) metamorphic rocks from Lützow–Holm Complex, East Antarctica show a systematic difference between sulfide assemblages in the rock matrix and those found as inclusions in the silicates stable in high-temperatures. Matrix sulfides are commonly pyrite with or without pentlandite and chalcopyrite. On the other hand, inclusion sulfides are pyrrhotite with or without pentlandite and chalcopyrite lamellae. When recalculated into integrated single-phase sulfide compositions, inclusion sulfides from the UHT region showed a wider range of solid–solution composition than the inclusion sulfides from the HT region. The host minerals of the sulfides with extreme solid–solution compositions are those stable at the peak of metamorphism such as orthopyroxene and garnet. One of the most extreme ones is included in orthopyroxene coexisting with sillimanite ± quartz, which is the diagnostic mineral assemblage of UHT metamorphism. These observations suggest that sulfide inclusions preserve their peak metamorphic compositions. Pyrrhotite did not revert to pyrite because of the closed system behavior of sulfur in inclusion sulfides. On the other hand, in the rock matrix where the open system behavior of sulfur is permitted, original sulfides were partly to completely altered by the later fluid activity.     

东沙海域浅层沉积物硫化物分布特征及其与天然气水合物的关系

对南海东沙海域浅层沉积物中硫化物的含量进行了分析,结果表明,沉积物中硫化物的含量与沉积物顶空气甲烷含量有密切的关系,在存在顶空气甲烷高异常的沉积物岩心中,沉积物中硫化物含量明显高于无甲烷异常的沉积物岩心,且随层位深度的增加,其含量明显增大,存在显著的变化梯度带。碎屑矿物鉴定结果表明,沉积物中硫化物主要以黄铁矿的形式存在。浅层沉积物中高含量的硫化物与天然气水合物分解形成的甲烷流有直接的关系,反映了下部沉积物中可能存在天然气水合物。     

Phosphorus-bearing sulfides and their associations in CM chondrites

Phosphorus-bearing Fe and Ni sulfides represent a new type of phosphorus compounds and are characteristic accessory phases of CM chondrites. The proportions of atoms in the sulfides can be approximated by the equation (Fe + Ni)/P = 0.965 ± 0.003 (1σ) · S/P + 1.255 ± 0.036 (1σ). Sulfides with high S/P ratios are systematically richer in Fe and poorer in Ni compared with low-S/P sulfides. Their characteristic minor elements are Cr, Ca, Co, K, and Na. The contents of Cr and Ca may reach several weight percent, but their incorporation does not affect the relation between (Fe + Ni)/P and S/P. This is also true of light elements (O and H), which probably occur in the P-bearing sulfides in certain amounts. The sulfides are usually associated with schreibersite, barringerite, eskolaite, and daubreelite. A negative correlation was observed between the Fe/Ni ratios of coexisting P-bearing sulfides and phosphides. Metallic iron was never found in association with the sulfides. It can be suggested that P-bearing sulfide is a primary phase rather than a secondary alteration product formed under the conditions of the CM chondrite parent body. This phase had to be stable in the solar nebula after the formation of Ca-Al inclusions and before the condensation of Fe-Ni metal. At high temperatures, P-bearing sulfide with low Fe/Ni and S/P ratios coexists with schreibersite in the solar gas. During condensation schreibersite is replaced by barringerite, which is accompanied by a decrease in the Fe/Ni ratio of phosphides and an increase in the S/P and Fe/Ni ratios of P-bearing sulfides. Trace element data suggest that the P-bearing sulfides could be formed in the solar nebula by the sulfidization of a precursor phase of extrasolar origin.     

柿竹园和香炉山W多金属矿床中硫化物微量元素特征:来自原位LA-ICP-MS分析

华南包括两个世界级的W矿带,分别是南岭和江南造山带W成矿带。柿竹园W多金属矿床位于南岭地区,香炉山W矿床位于江南造山带东北部。两个矽卡岩W矿床都发育硫化物成矿阶段。但硫化物和成矿元素组成存在显著的差异。前者由含Pb、Zn、Ag硫化物和黝铜矿、银黝铜矿、含Ag斜方辉铅铋矿和铁硫锡铜矿硫盐组成;后者主要为磁黄铁矿。柿竹园远接触带Pb-Zn-Ag矿脉中硫化物(闪锌矿、黄铜矿、方铅矿和磁黄铁矿)较富集B、Mn、Cr、Sb、Sn和Hg,香炉山似层状矽卡岩和硫化物-白钨矿矿体中硫化物(磁黄铁矿、黄铜矿和闪锌矿)较富集W、Se和Bi。两个矿床中黄铜矿、闪锌矿和方铅矿较富集Ag,黄铜矿、闪锌矿富集In和Sn,闪锌矿还富集Cd。两个矿床中的硫化物微量元素分析表明与矽卡岩W矿成矿相关的硫化物可载有多种微量元素。这些元素参与到硫化物中程度由多种因素控制。具体如下,硫化物中B含量高低与成矿相关岩体中B含量相关;在相对高温和还原条件下,硫化物中W含量较高;闪锌矿中Mn和Cd与Zn发生取代作用; Cr可以一定程度进入到硫化物中,并受成矿流体中Cr含量影响; Se与S发生了一定程度的取代进入硫化物,并受流体中它的含量控制; Bi在闪锌矿与黄铜矿易形成固溶体;硫化物中Sb含量受初始流体中它的含量影响,方铅矿中易包裹一定的辉锑矿(Sb_2S_3)或含Sb的硫盐矿物; Ag是否形成独立的矿物相和进入哪些硫化物中,取决于流体中Ag的初始含量和硫化物的沉淀次序;硫化物中Hg的含量受温度影响。     

The mercury in sulfide deposits emplaced in volcanic suites

Massive sulfide deposits in the Pacific and Ural provinces have varying mercury contents. The latter is lower in metamorphosed ores than in unmetamorphosed or in young ones. Two varieties of cenozoic sulfide ores are distinguished: 1) products of subcontinental solfataric action with high mercury content in pyrites, accompanied by cinnabar, 2) products of postvolcanic activity in submarine suites with low mercury content in sulfides (Kurokotype). A distribution of mercury between coexisting sulfides (in descending rank) corresponds to the sequence: sphalerite-chalcopyrite-pyrite. During metamorphism, sulfides loose their mercury (pyrite in higher degree than chalcopyrite). It is possible that mercury vaporised from sulfides has some influence on the formation of mercury ores at some distance from metamorphosed sulfide bodies within the same region.     

Sulfides in petroleum

The homologous series of terpenoid sulfides previously reported to be present in Athabasca bitumen have been detected in a variety of petroleums from the Western Hemisphere. All 22 samples examined, ranging in age from Devonoan to Cretaceous, contained the terpenoid sulfides. A method is described for the isolation of sulfides from petroleums based on the selective oxidation of sulfides to more polar sulfoxides which are easily removed from the mixture and their subsequent reduction to sulfides. The sulfide content in the petroleum maltenes examined ranged from 0.3 to 16.1% w/w. In addition to the bicyclic and tetracyclic terpenoid sulfides a new series of tricyclic terpenoid sulfides has been identified, and the details of the isoprenoid side chain have been elucidated for all three homologous series. The distributions by carbon number of the bicyclic and tetracyclic homologous series of terpenoid sulfides show pronounced variations which are attributed to thermal maturity and degree of water washing of the petroleum, thus the ability to identify terpenoid sulfides should provide a useful tool for oil-oil and oil-source rock correlation studies. The bicyclic and tricyclic terpenoid sulfides have the same carbon framework as the carotenoids which suggest that these sulfides were accessory pigments in photosynthesis.     

A Study of the Strathcona Mine and Its Bearing on the Origin of the Nickel-Copper Ores of the Sudbury District, Ontario

The Strathcona iron-nickel-copper sulfide ore deposit lies atthe base of the Sudbury Nickel Irruptive along the north rimof the Sudbury basin. In the vicinity of the deposit the mainbody of the Nickel Irruptive consists of an upper unit of 3700ft (1200 m) of granophyre (the ‘micropegmatite’)and a lower unit of 1500 ft (500 m) of augite norite (the ‘felsicnorite’) separated by 300 ft (100 m) of transitional rock(the ‘transition zone’). Two augite norite intrusions(the ‘mafic norite’ and the ‘xenolithic norite’)that are younger than the felsic norite occur along its lowercontact. The xenolithic norite is relatively rich in xenolithsand grades downwards into a unit known as the ‘hanging-wallbreccia’. The breccia resembles the xenolithic noritebut contains a higher proportion of xenoliths. A quartz-plagioclase-augite gneiss (the ‘footwall gneiss’)underlies all units of the Nickel Irruptive. A cataclastic breccia(the ‘footwall breccia’) which formed as a resultof comminution of both gneiss and overlying Irruptive rocksis present in most areas between the gneiss and the Nickel Irruptive.The ore body occurs partly as a dissemination of sulfides inthe matrix of the hanging-wall breccia (‘hanging-wallore’), partly as a fine dissemination and massive stringersof sulfide in the footwall breccia matrix (‘main-zoneore’), and partly as massive stringers of sulfide in thefootwall gneiss (‘deep-zone ore’). Xenoliths in the xenolithic norite and hanging-wall brecciarange from dunite to olivine gabbro. Olivine in the xenoliths(composition estimated by an X-ray method) varies from Fo73to Fo85, and hypersthene and augite (composition estimated byelectron microprobe analysis) vary from Fs25 to Fsi3, and Fsi3to Fs5, respectively. The iron content of the mafic mineralsshows a positive correlation with the proportion of felsic mineralsin the xenoliths, suggesting that the xenoliths have been derivedfrom a cryptically layered body of mafic and ultramafic rock.The wide distribution of xenoliths around the margin of theNickel Irruptive coupled with the absence of any obvious externalsource is strong evidence that the xenoliths are cognate, supportingWilson's (1956) proposal that the Irruptive is a funnel-shapedintrusion with a zone of ultramafic rocks towards its base. Hypersthene ranges from Fs33 to Fs28 in the felsic norite, fromFs28 to Fs22 in the mafic norite, and from Fs28 to Fs20 in thexenolithic norite. Augite ranges from Fsl6 to Fs14 in the felsicnorite and from Fs14 to Fsn in both the mafic and xenolithicnorites. The distribution coefficient for iron and magnesiumbetween coexisting augite and hypersthene ranges from 1-0 insome of the xenoliths to 1-5 in some samples of felsic norite,indicating that the two pyroxenes equilibrated at, or near,magmatic temperature. The composition of plagioclase in thefelsic norite, mafic norite, and xenolithic norite is aroundAn65-70 but decreases to An44 in those Irruptive rocks closestto the footwall breccia. The composition of plagioclase withinthe breccia varies between An32 and An43. Sodium metasomatismappears to have affected the breccia and to have spread outto affect adjacent rocks. The concentration of nickel and copper in the sulfides variessystematically across the ore deposit. The nickel content ofiron-nickel sulfides varies between 2-5 and 3 per cent in thehanging-wall ore but increases regularly from 3 per cent to5 or 5-5 per cent from hanging wall to footwall across the main-zoneore. Copper concentration shows a similar but more erratic variation.The variation is attributed to thermal diffusion of nickel andcopper within the main-zone ore along a gradient induced bythe overlying, hot, Nickel Irruptive. The principal opaque minerals in the ore body are, in the orderof their abundance, pyrrho-tite of at least two types, magnetite,pentlandite, chalcopyrite, and pyrite. All of the sulfides inthe hanging-wall ore are the result of exsolution from a high-temperature,pyrrhotite solid solution. Pyrite started to exsolve below 700C, chalcopyrite below 450 C, and pentlandite below 300 C.Monoclinic pyrrhotite formed from the host hexagonal pyrrhotiteprobably between 300 and 250 C. The temperature of formationof the sulfides in the main-zone ore has been obscured by reworkingof the ore after its first emplacement. The principal ore sulfides, pyrrhotite and pentlandite, arecommon throughout the mafic norite, xenolithic norite, and hanging-wallbreccia, occurring in amounts around 5 per cent in most samples.Pyrrhotite and pentlandite are extremely rare in the overlyingfelsic norite where pyrite is the most common sulfide. It occursin amounts between 01 and 0-5 per cent, commonly together withsecondary amphibole after pyroxene. The sulfides in the maficand xenolithic norites and in the hanging-wall breccia occupyspaces interstitial to the silicates, and little or no replacementof silicates by sulfides has occurred. In the main-zone ore,evidence of small-scale replacement of silicates by sulfidesis common. The high percentage of pyrrhotite and pentlandite in the maficand xenolithic norites in contrast to the felsic norite, texturalrelations between sulfides and silicates, and the high temperaturesindicated by the pyroxene distribution coefficients lead tothe conclusion that the hanging-wall sulfides (including thehanging-wall ore) at Strathcona were introduced with these youngernoritic intrusions. Data on the solubility of sulfides in silicatemagmas rule out the possibility that the bulk of the sulfideswere in solution in the noritic magmas; the data support thehypothesis that during intrusion the sulfides were held in suspensionin the in the magmas as droplets of immiscible sulfide-oxideliquid. Calculations on the rate of settling to be expectedfor such sulfide droplets are consistent with this hypothesis.The manner of emplacement of the main-zone ore is less certain;our explanation is that this ore consists of sulfides that originallysettled out of, or collected along, the base of the hanging-wallbreccia zone and were subsequently incorporated in the brecciationthat gave rise to the footwall breccia. The origin of the sulfides at Strathcona is clearly connectedclosely with the origin of the younger noritic intrusions. Asimilar connexion exists between sulfides and young marginalintrusions at many other Sudbury deposits. Jt is possible thatboth sulfides and intrusions are portions of the Nickel Irruptivemagma that lagged behind the main body of magma and were intrudedat a later stage. Alternatively, the young intrusions may haveassimilated sulfides from a sulfide-rich zone within or at themargin of the deeper layers of the Irruptive.     

Occurrences of iron sulfides in Ohio coals

The iron sulfides in seven different Ohio coals have been studied by polished-section ore microscopy, scanning electron microscopy augmented with EDS analyses, and secondary ion mass spectrometry. The iron sulfides in the coals exhibit a large array of textures and interrelationships which reflect site-specific environmental changes that occurred during the deposition of the sulfides. Sulfide deposition occurred principally during the depositional and diagenetic phases of the formation of the precursor peats. Pyrite and marcasite are present in most of the samples examined. Pyrite occurs as isolated and clustered euhedra, isolated and clustered framboids and spheres, cell-fillings, cleat- and fracture-fillings, replacements of plant debris, and as a porous or spongy-textured variety deposited within and around sulfide masses and grains. Marcasite occurs as polycrystalline spheres, polycrystalline rims and bands within and around clusters of pyrite spheres and framboids, as cell-fillings, and as replacements of plant debris. A typical sequence of iron sulfide deposition in texturally complex sulfide grains and masses is: (1) pyrite framboids or spheres; (2) deposition of marcasite around the relict framboids and clusters of framboids; and (3) spongy pyrite deposited as an outer fringe around sulfide masses and as infillings within the masses. The sulfides exhibit a persistent, although not universal, association with clays, and it is likely that much of the iron now present as sulfides was delivered to the depositional environment adsorbed on clay minerals. The iron sulfides tend to be localized in zones parallel to the banding in the coals. Such localization is most pronounced with respect to specific varieties of iron sulfides such as marcasite spheres, pyrite framboids, zones of pyrite euhedra, and occurrences of texturally complex grains and masses. Such zones are believed to represent depositional environments favorable for the precipitation of specific types of iron sulfides. These stratigraphic microenvironments changed during the times of deposition and diagenesis of the precursor peats and resulted in sequential deposition of the different forms of iron sulfides particularly evident in texturally complex sulfide grains. Chemically significant variables most likely were pH and availability of certain trace elements. The factors favoring precipitation of marcasite rather than pyrite are not clearly understood.The textures of the iron sulfides will prove to be important in understanding the reactivity of pyrite and marcasite in causing acid mine drainage and possibly spontaneous combustion of coal and mine waste, and will be important in the continuing development of effective methods of coal cleaning.     

冲绳海槽Jade热液活动区块状硫化物的铅同位素组成及其地质意义

新测行Ｊａｄｅ热液活动区中５件块状硫化物样品的铅同位素组成,具有较小的变化范围,表现出较均一的铅同位素组成特征。在Ｐｂ－Ｐｂ图解上,块状硫化物的铅同位素数据构成线形排列,与该区沉积物和蚀变火山岩的铅同位素组成一致,而与该区新鲜火山岩相比具较高的放射成因铅,证实了该区海底块状硫化物中的铅是由沉积物长英质火山岩来源铅共同构成的混合铅。不同热液活动区铅同位素组成对比研究表明,地质－构造环境的不同是导致各     

滇中播卡铜矿床硫、铅同位素组成及其地质意义

滇中播卡铜矿床是著名“东川式”铜矿床的典型代表,但对其成矿物质来源和矿床成因认识存在争议。对矿区典型铜矿发育的金属硫化物进行硫和铅同位素组成分析,探讨其成矿物质来源。硫同位素测试结果表明,人占石铜矿金属硫化物的δ³⁴S值为1.6‰~10.7‰,指示硫以岩浆(火山喷发)作用为主要来源,并受到沉积作用影响。铅同位素测试结果则表明人占石铜矿、天生塘铜矿、竹箐凹子铜矿和白石岩铜矿中的铅主要来源于壳幔混合物质。综合前人研究和本次硫、铅同位素分析结果,认为播卡铜矿床成矿物质主要来自地幔,且受到地壳物质的混染。     

Ore petrology of chromite-PGE mineralization in the Kempirsai ophiolite complex

Summary The platinum group minerals (PGM) in chromite ores of the Kempirsai ophiolite massif, located south of the Ural Mountains, are extremely varied in composition and represented predominantly by alloys, sulfides, arsenides, and sulfosalts of the iridium-group PGE (IPGE). The earlier Ir-Os-Ru alloys prevail over the later Cu-Os-Ru, Cu-Ir, Ni-Ir, Ni-Os-Ir-Ru, and Ni-Ru-Os-Fe alloys rich in base metals (BM). The earlier Ru-Os disulfides crystallize coevally with Ir-Os-Ru alloys, whereas the later sulfides are represented by compounds with a variable stoichiometry and a wide miscibility of Ni, Cu, Ir, Rh, Os, and Fe. Phase relations of PGE alloys with PGE-BM alloys, sulfides and sulfoarsenides confirm that deposition of these minerals was defined by a general evolution of PGE fractionation in the mineral-forming system but not by a super-imposed process. The leading mechanism of PGM crystallization is thought to be their dendritic growth during gas-transport reactions from low-density gaseous fluid enriched in PGE. The representative technological sampling of 0.5 million tons of an ore showed that the average PGE content in chromite ore is 0.71 ppm which leads to an evaluation of the PGE resources to be no less than 250 tons. Hence, the Kempirsai deposit is not only a giant chromium deposit, but also a giant deposit of IPGE: Ir, Ru, and Os. The size parameters of PGM and their aggregates suggests that the PGE may be recoverable in separate concentrates. Author’s address: Vadim Vadimovich Distler, Institute of Geology of Ore Deposits, Mineralogy, Petrography and Geochemistry Russian Academy of Sciences (IGEM RAS), Staromonetny 35, 119017 Moscow, Russia     

Geological context,mineralization, and timing of the Juramento sediment-hosted stratiform copper–silver deposit,Salta district,northwestern Argentina

The Juramento deposit in northwestern Argentina exhibits several readily visible general characteristics of sediment-hosted stratiform copper (SSC) mineralization. It consists of fine-grained disseminated base-metal sulfides within marine to lacustrine graybeds (the basal whitish Late Cretaceous Lecho Sandstone and shallow-water carbonates of the overlying Maastrichtian Yacoraite Formation) that overlie a thick sequence of redbeds (the Pirgua Subgroup). The property has been examined and drilled in three successive exploration programs as a possible analog of world-class mineralization in the copperbelts of central Africa and the Kupferschiefer. The present report provides specific field and laboratory results that confirm the classification as SSC-type mineralization. The host graybeds are the basal sandstone and overlying oolitic and stromatolitic units of the Yacoraite Formation, which are shown from textural studies to be carbonaceous and to have initially contained very fine-grained, disseminated, syndiagenetic pyrite. These sediments would have been sufficiently porous and permeable in early diagenetic time to allow an infiltration of metalliferous fluids from the underlying redbeds, resulting in the observed progressive replacement of in situ pyrite by common base-metal sulfides (sphalerite, galena, argentiferous tetrahedrite, and copper-rich sulfides: first chalcopyrite, then bornite, and finally chalcocite). Sulfur isotope analyses indicate that a portion of the sulfur of ore-stage sulfides is isotopically heavier than that of pyrite, possibly due to a contribution from associated gypsum. Ore-stage sulfides are zoned vertically and obliquely through the mineralized zones, from cupriferous sulfides at low stratigraphic levels to lead- and zinc-rich mineralization above, with unreplaced pyrite remaining within upper Yacoraite strata. The zoned sulfides and their replacement textures, the peneconformable configuration of the mineralized zones, and the position of ore-stage mineralization adjacent to a stratigraphically defined redox transition from redbeds upward into graybeds indicate an overprint of copper (and accompanying ore-stage metals) on originally pyritic graybeds. The influx of ore-stage metals, presumably in an oxidized low-temperature brine, terminated with a silicification event that effectively sealed the host carbonates. These observations and the overall genetic interpretation are consistent with the general deposit-scale genetic model for early diagenetic SSC mineralization. The regional geologic context is also consistent with its classification as a SSC deposit: It is hosted by post-oxyatmoversion sediments and was formed in association with evaporites at a low paleolatitude in a major intracontinental rift system.     

A tale of elemental accumulation and recycling in the metamorphosed Keketale VMS-type Pb-Zn deposit,Altai Mountains

The elemental accumulation and recycling in the metamorphosed Keketale VMS-type Pb-Zn deposit of the Altai Mountains are presented in this study. Based on detailed fieldwork and microscopic observation, the formation of the deposit involved syngenetic massive sulfide mineralization and epigenetic superimposed mineralization. Different generations of iron sulfides (i.e., pyrite and pyrrhotite) with contrasting textural, elemental, and sulfur isotopic features were generated in primary mineralization (including hydrothermal iron sulfides, colloform pyrite) and secondary modification (including annealed iron sulfides, oriented iron sulfides, and vein-pyrite). It is revealed that the spatial variation in textures and elements of hydrothermal iron sulfides depends on the inhomogeneous fluid compositions and varied environment in VMS hydrothermal system. Both leached sulfur from the footwall volcanic rocks and reduced sulfur by the TSR process are regarded as important sulfur sources. Furthermore, large sulfur isotopic fractionation and negative δ³⁴S values were mainly caused by varied oxygen fugacity, and to a lesser extent, temperature fluctuation. The epigenetic polymetallic veins that contain sulfides and sulfosalts (e.g., jordanite-geocronite, bournonite-seligmannite, boulangerite) were considered as the products of metamorphic fluid scavenged the metal-rich strata. All things considered, it is indicated that two episodes of fluid with distinct origins were essential for the formation of the deposit. The predominant evolved seawater along with subordinate magmatic fluid mobilized metals from volcanic rocks and precipitated massive sulfides near the seafloor are vital for primary mineralization. The metamorphic fluid remobilized metals (i.e., FMEs: fluid mobile elements, e.g., Pb, As, Sb) from neighboring volcanic and pyroclastic rocks and destabilized them within the fractured zone are responsible for secondary mineralization, which enhances the economic value of the deposit. Accordingly, metal-rich Devonian strata had been successively swept by different origins of fluid, leading to progressively elemental enrichment and the formation of a large deposit. Furthermore, the current study enlightens that FME-bearing veins with economic benefits can be discovered near the metamorphosed VMS deposits.     

Structure and age of the Cerro de Pasco Cu-Zn-Pb-Ag deposit,Peru

The world-famous Cu-Zn-Pb-Ag deposit at Cerro de Pasco, Peru, consists of texturally massive pyrite, texturally massive sphalerite-galena-pyrite, and veins containing pyrite and enargite. Historically the deposit has been considered to be the hydrothermal product of the adjacent Miocene volcanic and intrusive complex (locally known as the Vent). However, both the texturally massive sulfides of the deposit and the pre-Miocene strata are cut by the Longitudinal fault, one of the largest faults in the district, but the Vent is not. Imbrication by the Longitudinal fault zone (duplex structures) has thickened the deposit so that it is amenable to open-pit mining. Dikes and pyrite-enargite veins pass from the Vent into the massive sulfides; fragments of massive pyrite occur in the Vent. Thus, no matter what their origin, the texturally massive sulfides are older and, therefore, genetically unrelated to the Vent.     

高镍铜镍矿床的特征、形成机制与勘查展望

岩浆铜镍矿床100%硫化物中的Ni含量与赋矿岩石和成矿过程紧密相关,记录岩浆成分、分异程度与硫化物演化过程。硫化物异常高镍(高镍硫化物)往往被认为与科马提质岩浆或者后期热液作用密切相关。近年研究结合勘查证实,赋含高镍硫化物的矿床(高镍铜镍矿床)不仅限于科马提岩,还与苦橄质、玄武质岩浆有关,另外,热液富集作用并不是必要因素。本文总结了世界上高镍铜镍矿床的基本特征和形成机制,分析提出了不同机制的判别标志,并展望了其勘查前景。详细对比高镍铜镍矿床的产出环境、赋矿岩相、矿石特征、矿物组合等特征,该类矿床往往产于大陆裂谷和造山带环境,与基性程度较高的岩浆有关,以橄榄岩赋矿为主,含镍硫化物组合主要为镍黄铁矿-磁黄铁矿-黄铜矿组合,少数为针镍矿-镍黄铁矿-黄铁矿组合。科马提岩相关矿床可将Ni含量大于16%的硫化物定义为高镍硫化物,苦橄质-玄武质岩浆相关矿床的硫化物可分为高镍硫化物(Ni10%)、中镍硫化物(5%～10%)和富铜硫化物(Ni5%,CuNi)。原生高镍硫化物可由富镍岩浆熔离、硫化物从橄榄石中吸取Ni、硫化物结晶分异、硫化物与硫不饱和岩浆反应等机制形成。苦橄质-玄武质岩浆相关的矿床,硫化物与橄榄石的Fe-Ni交换反应是高镍硫化物形成的重要机制。辉石岩源区地幔部分熔融形成富镍岩浆是否为高镍硫化物形成的必要条件尚存争议。不同机制形成的高镍硫化物具有迥异的岩石-矿物组合和地化特征。硫化物矿物组合、橄榄石成分(Fo值、Ni含量、Fo值-Ni含量的相关性)、伴生元素(铜、铂族元素)丰度-配分模式等特征可作为区分不同高镍硫化物形成机制的有效指标。我国新疆黄山南、坡一和青海夏日哈木矿床(部分浸染状矿化橄榄岩)以赋含高镍硫化物为特征,新疆喀拉通克矿床的硫化物则以富铜为特征,中国其余矿床的硫化物均属中镍硫化物。目前研究指示中国的高镍铜镍矿床与母岩浆相对富镍、硫化物与橄榄石Fe-Ni交换作用密切相关,后者可使硫化物Ni含量提升3%～5%。在铜镍矿床勘查方面,稀疏-中等浸染状高镍硫化物矿石即可达到工业品位,稠密浸染状-块状高镍硫化物矿石可达到很高的Ni品位(10%),是高品位镍矿勘查的一个重要方向。造山带环境富水、相对高氧逸度(可高达QFM+1)的岩浆可能是形成高镍硫化物的有利条件,该环境橄榄石Fo值较高(87mol%)的岩体有利于形成高镍硫化物。     

贵州丹寨老东寨铅锌矿床稀土元素和硫同位素地球化学特征

老东寨铅锌矿床是黔东南地区近年来新发现的中型铅锌矿床,主矿体赋存于震旦系陡山沱组中,该矿床尚未有地球化学等方面的研究报道,导致对其成因机制知之甚少.本研究在系统分析矿床地质的基础上,对该矿床开展硫化物和围岩稀土元素及硫化物S同位素地球化学研究,为厘清其成因机制提供地球化学依据.结果表明硫化物稀土元素含量较低(∑REE=...     

Sulfides in mantle peridotites from Penghu Islands, Taiwan: Melt percolation, PGE fractionation, and the lithospheric evolution of the South China block

Major elements, highly siderophile elements (HSE) and Re-Os isotope ratios were analysed in situ on individual sulfide grains in spinel peridotite xenoliths hosted by Miocene intraplate basalts from the Penghu Islands, Taiwan. The xenoliths represent texturally and compositionally different mantle domains, and the geochemical characteristics of the sulfides show changes in HSE distribution and Re-Os isotope systematics, produced as their host rocks were metasomatised by percolating fluids/melts. In prophyroclastic and partly metasomatised peridotites from the Kueipi (KP) locality, the sulfides have subchondritic to superchondritic ¹⁸⁷Re/¹⁸⁸Os and ¹⁸⁷Os/¹⁸⁸Os ratios. Many of these sulfides reflect fluid/melt interaction with residual MSS and/or crystallization of fractionated sulfide melts, which produced high contents of Cu and PPGEs and high Re/Os; inferred melt/rock ratios are low. In contrast, sulfides in equigranular and extensively metasomatised peridotites from the Tungchiyu (TCY) locality are mainly more sulfur-rich Ni-(Co)-rich MSS, with subchondritic to chondritic ¹⁸⁷Os/¹⁸⁸Os and subchondritic ¹⁸⁷Re/¹⁸⁸Os. These sulfides are interpreted as products of interaction between pre-existing MSS and percolating silicate melts. Melt/rock ratios were high and the percolating melt was less differentiated than the melt that percolated the KP peridotites. Sulfides in a TCY pyroxenite are mainly MSS; they have the lowest HSE contents, subchondritic to superchondritic ¹⁸⁷Os/¹⁸⁸Os and subchondritic ¹⁸⁷Re/¹⁸⁸Os, and may have precipitated from sulfide melts that segregated from basaltic melts under S-saturated conditions. In most sulfides melt percolation appears to have induced fractionation among the HSEs and disturbed Re-Os isotope compositions. Despite the metasomatic effects, rare residual MSS, sulfides that from crystallised sulfide melts and sulfides modified by addition of Re (with no evidence for Os addition) can still provide useful chronological information. Such sulfides yield T_RD age peaks of 1.9, 1.7-1.6, 1.4-1.3 and 0.9-0.8 Ga, which may record the timing of melt extraction and/or metasomatic events in the mantle. These periods are contemporaneous with the major crustal events recorded by U-Pb dates and Nd and Hf model ages in the overlying crust. This close correspondence indicates that the sulfide T_RD ages reflect the timing of lithosphere-scale tectonothermal events (such as melting and metasomatism) that affected both the lithospheric mantle and the overlying crust. The sulfide T_RD ages, taken together with the crustal data, suggest that most of the Cathaysia block had formed at least by Paleo-Proterozoic time, and that some domains are Archean in age.