Geology,geochemistry, sulfur isotope composition,and fluid inclusion data of Farsesh barite deposit,Lorestan Province,Iran

Farsesh barite in the central part of Iranian Sanandaj-Sirjan zone is a sample of epigenetic hydrothermal mineralization in dolomitized limestone, which provides appropriate chemicophysical conditions making the passage of mineral-bearing fluids possible. Barite veins may range from a few centimeters to 2 m in thickness that increases downward. The microthermometry measurements obtained from more than 30 fluid inclusions show relative homogenization temperatures ranging from 125 to 200 °C with an average of 110 °C for Farsesh barite deposits. The mean salinity measured proves 16 times as much as weight percentage of NaCl for barite. Coexistence of liquid- and vapor-rich fluid inclusions in barite minerals may provide an evidence of boiling in ore veins. Moreover, occurrence of bladed calcite, high-grade ore zones, and presence of hydrothermal breccia are all consistent with boiling. Thermometric studies indicate that homogenization temperatures (Th) for primary and pseudosecondary fluid inclusions in barite range from 125 to 200 °C with an average of 1,100 °C. The δ³⁴S values of barite also lie between 8.88 and 16.6 %. The relatively narrow spread in δ³⁴S values may suggest uniform environmental conditions throughout the mineralization field. Thus, δ³⁴S values are lower than those of contemporaneous seawater, which indicates a contribution of magmatic sulfur to the ore-forming solution. Barite is marked by total amounts of rare Earth elements (REEs) (6.25–17.39 ppm). Moreover, chondrite-normalized REE patterns of barite indicate a fractionation of light REEs (i.e., LREEs) from La to Sm, similar to those for barite from different origins. The La_CN/Lu_CN ratios and chondrite-normalized REE patterns reveal that barite in Farsesh deposit is enriched in LREEs compared with heavy rare Earth elements (HREEs). Similarity between Ce/La ratios in barite samples and those found in deep-sea barite supports its marine origin. Lanthanum and Gd exhibit positive anomalies, which are common features of chemical marine sediments. Cerium shows a negative anomaly in most samples inherited from the negative Ce anomaly of hydrothermal fluid that is mixed with seawater at barite precipitation. The available data including tectonic setting, host rock characteristics, REE geochemistry, and sulfur isotopic compositions may support a hydrothermal submarine origin for Farsesh barite deposit.     

Rare earths in barites: distribution and effects on aqueous partitioning

A large variety of barites collected from marine and continental environments was analyzed by neutron activation for the rare-earth elements (REE) La, Ce, Sm, Eu and Dy. Relative to chondrites, all barites show a decrease of the lighter REE from La toward Eu. The abundance and distribution of rare earths in barites show a distinction of barite types. Deep-sea barites have large REE concentrations as do other authigenic deep-sea minerals and display the chondrite normalized Eu minimum, but not the negative Ce anomaly, of sea water. Other barites, mostly on land, some hydrothermal, and others of shallow marine origin, display lower total Ree concentrations. Chondrite normalized positive Eu anomalies are displayed by those varieties of reducing sedimentary and metamorphic origin.Distribution of REE in barite can be attributed both to crystallographic constraints of substitution, and to solution complexing of REE in the precipitating medium. Plots of rare earth partitioning versus effective ion size suggest that the decreasing enrichment toward Eu for all barite types is caused by crystallographic constraints due to contraction of the substituting REE ion sizes relative to the size of the host Ba ion. Solution effects on REE substitution in barite can be evaluated by writing solid solution distribution equations based on mass action of REE and Ba sulfates and the lanthanide (Ln) solution species Ln (CO₃)^?5₄), LnSO⁺₄, LnCl⁺² and LnF⁺². Under normal sea water conditions, solution complexing plays a minor role. However, increased alkalinities of reducing sediments and increased brine chlorinities could cause significant complexing and deplete REE heavier than Eu. Besides Dy in barites, this could be true for aqueous precipitation of REE in general.     

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     

Barite in the ocean – occurrence,geochemistry and palaeoceanographic applications

The mineral barite (BaSO₄) can precipitate in a variety of oceanic settings: in the water column, on the sea floor and within marine sediments. The geological setting where barite forms ultimately determines the geochemistry of the precipitated mineral and its usefulness for various applications. Specifically, the isotopic and elemental composition of major and trace elements in barite carry information about the solution(s) from which it precipitated. Barite precipitated in the water column (marine or pelagic barite) can be used as a recorder of changes in sea water chemistry through time. Barite formed within sediments or at the sea floor from pore water fluids (diagenetic or cold seeps barite) can aid in understanding fluid flow and sedimentary redox processes, and barite formed in association with hydrothermal activity (hydrothermal barite) provides information about conditions of crust alteration around hydrothermal vents. The accumulation rate of marine barite in oxic‐pelagic sediments can also be used to reconstruct past changes in ocean productivity. Some key areas for future work on the occurrence and origin of barite include: fully characterizing the mechanisms of precipitation of marine barite in the water column; understanding the role and potential significance of bacteria in barite precipitation; quantifying parameters controlling barite preservation in sediments; determining the influence of diagenesis on barite geochemistry; and investigating the utility of additional trace components in barite.     

Genesis of the Jinding Zn-Pb deposit,northwest Yunnan Province,China: Constraints from rare earth elements and noble gas isotopes

The giant sediment-hosted Jinding zinc-lead deposit is located in the Lanping Basin, northwestern Yunnan Province, China. The genesis of the deposit has long been debated and the sources of the ore-forming fluids and metals are controversial. This study presents rare earth element (REE) and noble gas isotope data that constrain the origins of the ore fluids and the heat source driving the hydrothermal circulation. The early-stage sulfides are enriched in light REEs and have high ∑REE values (30.8–94.8 ppm) and weakly negative Eu (δEu 0.85–0.89) and Ce anomalies (δCe 0.84–0.95), suggesting that the fluids were likely derived from dissolution of Upper Triassic marine carbonates with input of REEs from aluminosilicate rocks in the basin. In contrast, the late-stage sulfides have irregular REE patterns, generally low ∑REE values (0.24–10.8 ppm) and positive Eu (δEu 1.22–10.9) and weakly negative Ce anomalies (δCe 0.53–0.90), which suggest that the ore-forming fluids interacted with evaporite minerals. The ³He/⁴He (0.01–0.04 R_a) and ⁴⁰Ar/³⁶Ar values (301–340) of the ore-forming fluids indicate crustal and atmospheric origins for these noble gases. These findings are in agreement with the published fluid inclusion microthermometry data and the results of H, O, C, S, Pb and Sr isotope studies. Our data, in combination with published results, support a two-stage hydrothermal mineralization model, involving early-stage basinal brines and late-stage meteoric water that acquired metals and heat from crustal sources.     

四川冕宁稀土矿床脉石矿物的微量及稀土元素地球化学特征

包裹体地球化学研究表明，四川冕宁稀土矿床中存在着岩浆成因的萤石、重晶石和方解石，它们的微量元素地球化学特征与热液成因对应矿物有明显差别：岩浆成因重晶石相对富集亲石元素，贫亲硫元素；无论是岩浆成因重晶石，还是萤石均明显富集挥发分。稀土元素地球化学研究显示，不同成因萤石、重晶石在稀土元素总量、ＬＲＥＥ／ＨＲＥＥ、（Ｌａ／Ｙｂ）Ｎ、δＥｕ及δＣｅ等一系列稀土元素地球化学参数上都存在明显的差异。该项研究还揭示了岩浆成因萤石、重晶石是在相对还原和酸性体系内结晶而成的。     

重晶石沉积类型及成因评述--兼论扬子地区下寒武统重晶石的富集机制

重晶石沉积类型丰富,具有多种成因过程。通常,沉积型重晶石可分为生物、热液、成岩和冷泉重晶石四种类型。富钡与富硫酸盐的流体（海水、早成岩孔隙水或热液流体）及其相互作用过程（水柱、热液系统、沉积柱、沉积物-水界面附近）决定了重晶石的沉积环境、宏微观产出方式、同位素组成及相应的地质意义。另外,根据扬子地区下寒武统富重晶石沉积的地质特征,简述了其各种富集机制的适用性及争论。据此建议,结合埃迪卡拉纪-寒武纪转折时期的古海洋背景,对其进行详细的沉积学及地球化学分析,有助于深化成因认识,弥合分歧。     

The vein-type barite mineralization of the Draïssa ore field,Ougarta; SW- Algeria: mineralogy,trace elements and halogens

The Draïssa barite vein system in the Ougarta district is located in southwestern Algeria. It is the principal mineral deposit of economic interest of the area. The mineralization is hosted by Cambrian sedimentary rocks that unconformably overlie Precambrian formations. The mineralized structures consist mostly of barite and quartz with minor sulfide minerals and trend dominantly NE-SW, NW-SE, and E-W. Siliceous alteration zones are associated with the vein system. Samples of barite ore are characterized by low total REE contents ranging from 9 to 50 ppm and positive Eu (2–2.15 ppm) and Y (1.2–11.1 ppm) anomalies, indicating hydrothermal activity during mineralization. Halogen data of the barite show that the Cl/Br molar ratio is 189:571 and the Na/Br ratio is 34:376, indicating that the sulfur was derived from seawater. The Ba-enrichment trend in the volcanic rocks of Draïssa is interpreted as possible probable source of the Ba (424–3039 ppm Ba). It appears that the barite-quartz deposits were formed in two stages. Endogenous fluids deposited the primary vein materials, consisting of quartz associated with copper sulfides. Exogenous fluids (cold seawater) became heated during ascendant fluid movement. Mineralization was governed by convective motions and the barite and galena fillings were deposited in openings created by normal faulting.     

湖南应溪重晶石矿床地球化学特征及矿床成因

湖南新晃县应溪重晶石矿床赋存于贡溪复式向斜的早寒武世牛蹄塘组黑色页岩中，该向斜断层复杂．电子探针分析表明：矿石与围岩都含有钡长石．矿石与围岩的微量元素研究表明：Mo、V、Pb等微量元素强烈富集而大离子与高场强元素含量很低；矿石样品中U/Th比值大于1；矿床围岩稀土元素具有明显的正Eu异常．这些特征揭示该矿床是热水沉积型矿床．研究结果表明：断层为成矿热液提供了上涌通道；上升热液为矿床提供了钡离子，海水提供了硫酸根离子．在氧化条件下，钡离子与硫酸盐离子结合形成了重晶石矿床．     

Geochemistry of a sediment push-core from the Lucky Strike hydrothermal field,Mid-Atlantic Ridge

Hydrothermal sediment mineralogy and geochemistry can provide insights into seafloor mineralization processes and changes through time. We report a geochemical investigation of a short (22 cm) near-vent hydrothermal metalliferous sediment core from the Lucky Strike site (LS), on the Mid-Atlantic Ridge (MAR). The sediment was collected from the base of an active white smoker vent and comprises pure hydrothermal precipitates, mainly chalcopyrite, sphalerite, pyrite and barite, with negligible detrital and biogenic inputs. Geochemically, the core is enriched in elements derived from high-temperature hydrothermalism (Fe, Cu, Zn and Ba) and depleted in elements derived from low-temperature hydrothermalism (Mn), and metasomatism (Mg). The U/Fe content ratio is elevated, particularly in the deeper parts of the core, consistent with uptake from seawater associated with sulphide alteration. Rare earth elements (REE) concentrations are low and chondrite-normalized patterns are characteristic of high-temperature vent fluids with an enrichment in light REE and a pronounced positive Eu anomaly. A stronger positive Eu anomaly associated with higher La_n/Sm_n at the core top is controlled by barite precipitation. The hydrothermal influence on the REE decreases downcore with some evidence for a stronger seawater influence at depth. Nd isotopes also exhibit an increased detrital/seawater influence downcore. Pb isotope ratios are uniform and plot on the Northern Hemisphere Reference Line in a small domain defined by LS basalts and exhibit no detrital or seawater influence. Lucky Strike sediments are derived from high-temperature mineralization and are overprinted by a weak seawater–sediment interaction when compared with other Atlantic hydrothermal sites such as TAG. The larger seawater input and/or a larger detrital contribution in deeper layers can be explained by variable hydrothermal activity during sediment formation, suggesting different pulses in activity of the LS hydrothermal system.     

Rare earth element abundances in hydrothermal fluids from the Manus Basin, Papua New Guinea: Indicators of sub-seafloor hydrothermal processes in back-arc basins

Rare earth element (REE) concentrations are reported for a large suite of seafloor vent fluids from four hydrothermal systems in the Manus back-arc basin (Vienna Woods, PACMANUS, DESMOS and SuSu Knolls vent areas). Sampled vent fluids show a wide range of absolute REE concentrations and chondrite-normalized (REE_N) distribution patterns (La_N/Sm_N ∼ 0.6-11; La_N/Yb_N ∼ 0.6 - 71; ). REE_N distribution patterns in different vent fluids range from light-REE enriched, to mid- and heavy-REE enriched, to flat, and have a range of positive Eu-anomalies. This heterogeneity contrasts markedly with relatively uniform REE_N distribution patterns of mid-ocean ridge hydrothermal fluids. In Manus Basin fluids, aqueous REE compositions do not inherit directly or show a clear relationship with the REE compositions of primary crustal rocks with which hydrothermal fluids interact. These results suggest that the REEs are less sensitive indicators of primary crustal rock composition despite crustal rocks being the dominant source of REEs in submarine hydrothermal fluids. In contrast, differences in aqueous REE compositions are consistently correlated with differences in fluid pH and ligand (chloride, fluoride and sulfate) concentrations. Our results suggest that the REEs can be used as an indicator of the type of magmatic acid volatile (i.e., presence of HF, SO₂) degassing in submarine hydrothermal systems. Additional fluid data suggest that near-seafloor mixing between high-temperature hydrothermal fluid and locally entrained seawater at many vent areas in the Manus Basin causes anhydrite precipitation. Anhydrite effectively incorporates REE and likely affects measured fluid REE concentrations, but does not affect their relative distributions.     

S, C, O, H Isotope Data and Noble Gas Studies of the Maoniuping LREE Deposit, Sichuan Province, China： A Mantle Connection for Mineralization

The Maoniuping REE deposit, located about 22 km to the southwest of Mianning, Sichuan Province, is the second largest light REE deposit in China, subsequent to the Bayan Obo Fe-Nb-REE deposit in the Inner Mongolia Autonomous Region. Tectonically, it is located in the transitional zone between the Panxi rift and the Longmenshan-Jinpingshan orogenic zone. It is a carbonatite vein-type deposit hosted in alkaline complex rocks. The bastnaesite-barite, bastnaesite-calcite, and bastnaesite-microcline lodes are the main three types of REE ore lodes. Among these, the first lode is distributed most extensively and its REE mineralization is the strongest. Theδ34Sv-CDT values of the barites in the ore of the deposit vary in a narrow range of +5.0 to +5.1‰in the bastnaesite-calcite lode and +3.3 to +5.9‰in the bastnaesite-barite lode, showing the isotopic characteristics of magma-derived sulfur. Theδ13Cv-PDB values and theδ518OV-SMOW values in the bastnaesite-calcite lode range from -3.9 to -6.9‰and from +7.3 to +9.7‰, respectively, which fall into the range of "primary carbonatites", showing that carbon and oxygen in the ores of the Maoniuping deposit were derived mainly from a deep source. Theδ13Cv-PDB values of fluid inclusions vary from -3.0 to -5.6‰, with -3.0 to -4.0‰in the bastnaesite-calcite lode and -3.0 to -5.6‰in the bastnaesite-barite lode, which show characteristics of mantle-derived carbon. TheδDv-SMOW values of fluid inclusions range from -57 to -88‰, with -63 to -86‰in the bastnaesite-calcite lode and -57 to -88‰in the bastnaesite-barite lode, which show characteristics of mantle-derived hydrogen. Theδ18OH2OV-SMOW values vary from +7.4 to +8.6‰in the bastnaesite calcite lode, and +6.7 to +7.8‰in the bastnaesite-barite lode, almost overlapping the range of +5.5 to +9.5‰for magmatic water. The 4He content, R/Ra ratios are (13.95 to 119.58×10-6 (cm3/g)STP and 0.02 to 0.11, respectively, and 40Ar/36Ar is 313±1 to 437±2. Considering the 4He increase caused by high contents of radioactive elements, a mantle-derived fluid probably exists in the inclusions in the fluorite, calcite and bastnaesite samples. The Maoniuping deposit and its associated carbonatite-alkaline complex were formed in 40.3 to 12.2 Ma according to K-Ar and U-Pb data. All these data suggest that large quantities of mantle fluids were involved in the metallogenic process of the Maoniuping REE deposit through a fault system.     

贵州天柱大河边铅锌矿床的发现及其意义

大河边重晶石矿床是一个世界级的超大型重晶石矿床。最近在该区重晶石矿床下部的震旦系陡山沱组碳酸盐岩(白云岩)和碎屑岩中,新发现一套规模较大、层位产出稳定的铅锌矿化。铅锌矿体和重晶石矿床具有"上部为重晶矿,下部为铅锌硫化物矿床"的矿化特征。铅锌矿段矿石矿物主要为闪锌矿、黄铁矿及方铅矿,含少量白铁矿、黄铜矿及磁黄铁矿;脉石矿物主要为石英和重晶石,少量白云石、热液磷灰石、炭沥青及钡冰长石。成矿流体特征类似于形成沉积喷流型铅锌矿床的流体特征。铅锌矿化中的硫源自局限海盆内早寒武世海水经硫酸盐还原作用提供。此种类似于喷流沉积型铅锌矿床在南华裂谷盆地一带矿化层位稳定、分布范围较广泛,体现早寒武世时在裂谷盆地内存在一次大规模的热液事件。天柱大河边铅锌矿床的发现具有重要的资源意义及区内该种矿床的勘查意义。     

Origin of natural sulfur-metal chimney in the Tangyin hydrothermal field,Okinawa Trough: constraints from rare earth element and sulfur isotopic compositions

For the first time, we present the rare earth element (REE) and sulfur isotopic composition of hydrothermal precipitates recovered from the Tangyin hydrothermal field (THF), Okinawa Trough at a water depth of 1206 m. The natural sulfur samples exhibit the lowest ΣREE concentrations (ΣREE= 0.65×10^–6–4.580×10^–6) followed by metal sulfides (ΣREE=1.71×10^–6–11.63×10^–6). By contrast, the natural sulfur-sediment samples have maximum ΣREE concentrations (ΣREE=11.54×10^–6–33.06×10^–6), significantly lower than those of the volcanic and sediment samples. Nevertheless, the δEu, δCe, (La/Yb)_N, La/Sm, (Gd/Yb)_N and normalized patterns of the natural sulfur and metal sulfide show the most similarity to the sediment. Most hydrothermal precipitate samples are characterized by enrichments of LREE (LREE/HREE=10.09–24.53) and slightly negative Eu anomalies or no anomaly (δEu=0.48–0.99), which are different from the hydrothermal fluid from sediment-free mid-oceanic ridges and back-arc basins, but identical to the sulfides from the Jade hydrothermal field. The lower temperature and more oxidizing conditions produced by the mixing between seawater and hydrothermal fluids further attenuate the leaching ability of hydrothermal fluid, inducing lower REE concentrations for natural sulfur compared with metal sulfide; meanwhile, the negative Eu anomaly is also weakened or almost absent. The sulfur isotopic compositions of the natural sulfur (δ³⁴S=3.20‰–5.01‰, mean 4.23‰) and metal sulfide samples (δ³⁴S=0.82‰–0.89‰, mean 0.85‰) reveal that the sulfur of the chimney is sourced from magmatic degassing.     

Genesis for Rare Earth Elements Enrichment in the Permian Manganese Deposits in Zunyi,Guizhou Province,SW China

The Zunyi manganese deposits, which formed during the Middle to Late Permian period and are located in northern Guizhou and adjacent areas, are the core area of a series of large-medium scale manganese enrichment minerogenesis in the southern margin and interior of the Yangtze platform, Southern China. This study reports the universal enrichment of rare earth elements(REEs) in Zunyi manganese deposits and examines the enrichment characteristics, metallogenic environment and genesis of REEs. The manganese ore bodies present stratiform or stratoid in shape, hosted in the silicon–mud–limestones of the Late Permian Maokou Formation. The manganese ores generally present lamellar, massive, banded and brecciated structures, and mainly consist of rhodochrosite, ropperite, tetalite, capillitite, as well as contains paragenetic gangue minerals including pyrite, chalcopyrite, rutile, barite, tuffaceous clay rock, etc. The manganese ores have higher ΣREE contents range from 158 to 1138.9 ppm(average 509.54 ppm). In addition, the ΣREE contents of tuffaceous clay rock in ore beds vary from 1032.2 to 1824.5 ppm(average 1396.42 ppm). The REEs from manganese deposits are characterized by La, Ce, Nd and Y enriched, and existing in the form of independent minerals(e.g., monazite and xenotime), indicating Zunyi manganese deposits enriched in light rare earth elements(LREE). The Ce_(anom) ratios(average-0.13) and lithofacies and paleogeography characteristics indicate that Zunyi manganese deposits were formed in a weak oxidation-reduction environment. The(La/Yb)_(ch), Y/Ho,(La/Nd)_N,(Dy/Yb)_N, Ce/Ce* and Eu/Eu* values of samples from the Zunyi manganese deposits are 5.53–56.92, 18–39, 1.42–3.15, 0.55–2.20, 0.21–1.76 and 0.48–0.86, respectively, indicating a hydrothermal origin for the manganese mineralization and REEs enrichment. The δ~(13) C_(V-PDB)(-0.54 to-18.1‰) and δ~(18) O_(SMOW)(21.6 to 26.0‰) characteristics of manganese ores reveal a mixed source of magmatic and organic matter. Moreover, the manganese ore, tuffaceous clay rock and Emeishan basalt have extremely similar REE fractionation characteristic, suggesting REEs enrichment and manganese mineralization have been mainly origin from hydrothermal fluids.     

豫西嵩县上庄坪铅锌银矿床地球化学特征及地质意义

上庄坪铅锌银矿床是新一轮国土资源大调查中在北秦岭二郎坪群发现的硫化物矿床。笔者通过对矿床矿石、容矿同岩、重晶石岩的微量、稀土元素地球化学特征分析和地质特征研究,探讨成矿构造环境、成矿物质来源及矿床成因问题。研究表明.矿石和容矿围岩稀土元素球粒陨石标准化组成模式均为右倾型.矿石与围岩在Cu-Pb-Zn判别图解中投点区域一致.矿石Zn/(Zn Pb)与冲绳海槽和上向黑矿矿石特征相似、与TAG和EPR13°N区硫化物存在差异.矿石具较高As、Sb和Pb与低Cu、Cd和Se元素特征.认为该矿床成矿元素来源于壳幔混合、但以壳源为主的围岩变(石英)角斑岩和变细碧岩。矿石稀土元素、微量元素地球化学特征、矿床地质特征及与热水沉积重晶石岩和硅质岩的紧密共生关系说明,上庄坪矿床是弧后盆地构造环境海底热液喷流成岩成矿作用的产物。重晶石岩、硅质岩、矿床纵向和横向分带是寻找和勘探该类矿床的重要标志和依据。     

Geology, geochemistry and sulfur isotope composition of the Late Proterozoic Jingtieshan (Superior-type) hematite-jasper-barite iron ore deposits associated with stratabound Cu mineralization in the Gansu Province, China

The Jingtieshan deposit occurs in a Precambrian tectonic-stratigraphic terrane within the Northern Qilian Caledonian Orogen, and is generally considered as a Superior-type iron formation. The deposit is characterized by Fe-Si-Ba and Cu mineralization and consists of two types of orebodies, an upper jasper-barite-iron deposit and a lower copper sulfide deposit. The iron orebodies occur as independent stratigraphic layers concordant within a thick argillaceous succession, and exhibit fine-grained textures and well-developed sedimentary layering. The ores are predominantly composed of specularite and jasper with lesser amounts of magnetite, hematite, siderite, and barite. The presence of barite, hematite and jasper as major components shows that the iron ores were precipitated in a relatively oxidized ocean floor environment. The Cu orebody directly underlies the iron ore and is hosted by chlorite-sericite-quartz phyllite. The Cu mineralization is composed of pyrite and chalcopyrite and is characterized by stockwork. The disseminated and stockwork Cu mineralization is metamorphosed and concordant with respect to foliation, indicating pre-fabric development, i.e. pre-metamorphism, and was probably originally formed by reduced fluids reacting at the base of and within the oxide iron formation. Geochemical data show that the jasper-barite-iron ores, which resemble Superior-type iron formations, have a high input of hydrothermal-hydrogeneous elements (SiO₂, av.=56%; Fe₂O_3t, av.=30%; Mn, av.=0.45%; BaO, av.=16.7%) with minimal terrigeneous input (<15% combined Al₂O₃, TiO₂, K₂O, MgO, etc.). The δ³⁴S of exhalative barite varies from 28 to 34‰, which is very heavy with respect to other Late Proterozoic sulfate-bearing deposits, except those of circa 600 Ma in which the sulfides range from 8 to 20‰. The sulfur isotope data indicate that the barite was formed by the mixing of a Ba-rich hydrothermal fluid with sulfate-rich ambient seawater and that the sulfides ores were most probably derived from the reduction of seawater sulfate during subsurface reaction with ferrous iron-bearing minerals. These data are consistent with the jasper-barite-iron deposit forming by hydrothermal exhalative and chemical sedimentary processes on the floor of an ocean basin, and with the Cu mineralization forming by hydrothermal filling and replacement in base of and within the iron formation. Received: 19 March 1997 / Accepted: 14 May 1998     

Thermodynamic modeling of REE behavior in oxidized hydrothermal fluids of high sulfate sulfur concentrations

Thermodynamic calculations using the HCh software were made for mineral equilibriums including REEs in the fluoride–sulfide–chloride–carbonate–sulfate–system in the presence of Na, Ca, and P with fluids of various acidities–alkalinities [11]. The obtained thermodynamic characteristics of thenardite allowed us to carry out the calculations for this phase under complicated hydrothermal conditions simulating the presence of oxidized fluids at 500–100°C and 2000–125 bar. Among other solid phases, REEs–fluorite, monazite, and REE–F–apatite were formed as CaF₂–(Ln,Y)F₃, LnPO₄, and Ca₅(PO₄)₃F–(Ln,Y)₃(PO₄)₃ ideal solid solutions, respectively, where Ln is La, Ce, Pr, Nd, Sm, Eu, and Gd. Xenotime, anhydrite, elemental sulfur, and calcite were found as well.     

扬子板块北缘马元铅锌矿床两类矿石地球化学特征及其对成矿作用的制约

对马元铅锌矿白云石-硫化物型和重晶石-硫化物型矿石中的热液矿物白云石和重晶石的同位素和稀土元素地球化学特征对比研究表明,白云石的δ~(13)CPDB为-2.51×10-3~0.93×10-3,δ18OSMOW为17.55×10~(-3)~23.24×10~(-3),说明成矿流体中碳、氧来源于震旦系碳酸盐岩的溶解;锶同位素组成(0.711 46)表明Sr来源以壳源锶为主,可能与富放射性锶的上覆碎屑岩或下伏基底变质火山岩有关;稀土元素具有明显的正Eu异常(δEu平均为1.415),表明白云石-硫化物型矿化流体具有盆地中循环热卤水特点。重晶石的硫同位素(平均为33×10~(-3))具有富重硫且分布均一的特点,暗示硫可能来源于富集重硫的单一海相硫酸盐;Sr同位素(0.709 18~0.709 71)特征表明其来源以海水锶为主,有少量壳源锶加入;稀土元素具有明显负Ce异常(δCe平均为0.255)和正Eu异常(δEu平均为1.43),表明重晶石--硫化物型矿化有关的流体可能是海水(或大气降水)与盆地循环热流体混合的结果。白云石--硫化物型矿石和重晶石-硫化物型矿石的沉淀可能是盆地中循环热卤水与海水(或大气降水)两种端元组分以不同比例混合的结果。     

In-situ LA-ICP-MS trace elemental analyses of magnetite: The Bayan Obo Fe-REE-Nb deposit,North China

The Bayan Obo Fe-REE-Nb deposit in northern China is the world's largest light REE deposit, and also contains considerable amounts of iron and niobium metals. Although there are numerous studies on the REE mineralization, the origin of the Fe mineralization is not well known. Laser ablation (LA) ICP-MS is used to obtain trace elements of Fe oxides in order to better understand the process involved in the formation of magnetite and hematite associated with the formation of the giant REE deposit. There are banded, disseminated and massive Fe ores with variable amounts of magnetite and hematite at Bayan Obo. Magnetite and hematite from the same ores show similar REE patterns and have similar Mg, Ti, V, Mn, Co, Ni, Zn, Ga, Sn, and Ba contents, indicating a similar origin. Magnetite grains from the banded ores have Al + Mn and Ti + V contents similar to those of banded iron formations (BIF), whereas those from the disseminated and massive ores have Al + Mn and Ti + V contents similar to those of skarn deposits and other types of magmatic-hydrothermal deposits. Magnetite grains from the banded ores with a major gangue mineral of barite have the highest REE contents and show slight moderate REE enrichment, whereas those from other types of ores show light REE enrichment, indicating two stages of REE mineralization associated with Fe mineralization. The Bayan Obo deposit had multiple sources for Fe and REEs. It is likely that sedimentary carbonates provided original REEs and were metasomatized by REE-rich hydrothermal fluids to form the giant REE deposit.