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1.
From a mineralogical point of view the La Unión ore field (SE Spain) can be regarded as an oddity as some of its hydrothermal, stratabound type deposits display an extremely unusual paragenesis comprising magnetite ± greenalite ± minnesotaite ± siderite and galena ± sphalerite (IOSC – LZS). Recent mineralogical studies have shown that this paragenesis is also present at the neighboring Mazarrón ore field. These ore fields share a similar geologic setting, involving metamorphic and sedimentary rocks (Paleozoic s.l. to Permian) hosting late Miocene high‐K calc‐alkaline volcanic and subvolcanic rocks. The latter have andesitic to dacitic composition, and triggered hydrothermal activity and ore deposition. This study discusses the detailed mineral chemistry of magnetite samples from Mazarrón and La Unión and provides some hints for the origin of the IOSC – LZS paragenesis. We performed electron microprobe (EPMA) analyses in magnetite samples from La Unión and Mazarrón to determine the contents of minor and trace elements (Zn, Ni, Mn, Cr, V, K, Ca, Ti, Al, Si, Mg). Given that some results fell below the detection limit for the EPMA instrumental conditions we used robust regression on order statistics (robust ROS), with the NADA package in R to deal with these data sets. The Ca + Al + Mn contents in magnetites from San Cristóbal and Emilia are equivalent to the mean contents of those of IOCG, Kiruna, BIF, Cu porphyry, skarn, VMS, hydrothermal and clastic Pb–Zn deposits, but they are low in Ti + V and Ni + Cr. The principal components analysis indicates that Zn, Ni, Cr, V, K, Ca, Ti, and Mg are roughly collinear, therefore correlated, being also independent from Fe. Besides, the function discriminant analysis of data shows that the magnetites from Emilia and San Cristóbal cluster in differentiated groups, thus probably reflecting some differences related to the distance to the magmatic source that triggered the hydrothermal system: proximal in the case of San Cristóbal and distal in Emilia.  相似文献   

2.
The petrography and mineral chemistry of magnetite from fifteen volcanogenic massive sulfide (VMS) deposits in Canada, and the Lasail VMS deposit in Oman, as well as from two VMS-associated banded iron formations (BIF), Austin Brook (New Brunswick, Canada) and Izok Lake (Nunavut, Canada), were investigated using optical microscopy, electron probe micro-analyzer (EPMA), and laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS). The method of robust estimation for compositional data (robCompositions) was applied to investigate geochemical censored data. Among thirty-seven elements analyzed by EPMA and/or LA-ICP-MS in magnetite from the studied deposits/bedrock lithologies, only the results for Si, Ca, Zr, Al, Mg, Ti, Zn, Co and Ni contain < 40% censored values, and thus could be imputed using robCompositions. Imputed censored data were transformed using centered log-ratios to overcome the closure effect on compositional data. Transformed data were classified by partial least squares-discriminant analysis (PLS-DA) to identify different compositional characteristics of magnetite from VMS deposits and BIFs. The integration of petrography and mineral chemistry identifies three types of magnetite in VMS settings: magmatic, hydrothermal, and metamorphic. Magmatic magnetite in VMS deposit host bedrocks is characterized by ilmenite exsolution and may be overprinted by metamorphism. Some VMS deposits contain hydrothermal magnetite, which is intergrown with sulfides, and shows a metamorphic overprint as it is partly replaced by common metamorphic minerals including chlorite, sericite, anthophyllite, and/or actinolite, whereas the majority of the deposits are characterized by metamorphic magnetite formed by replacing pre-existing sulfides and/or silicates, and is intergrown with metamorphic minerals. Among VMS deposits of the Noranda mining district, the West Ansil deposit is characterized by hydrothermal-metamorphic magnetite zoned by inclusion-free cores and Si- and Mg-rich rims. Magnetite from the studied VMS-associated BIFs is also metamorphic in origin. Aluminum, Ti and Zn contents of magnetite can separate BIF from the other mineralized and un-mineralized bedrock lithologies in the studied VMS settings.PLS-DA shows that variable compositions of magnetite slightly discriminate different studied deposits/bedrock lithologies. The geochemical observations suggest that the variation in magnetite chemistry from different VMS settings might be sourced from differences in: 1) the composition and temperature of parental magmas or hydrothermal fluids, 2) the composition of host bedrocks, 3) the composition of co-forming minerals, and 4) oxygen fugacity. PLS-DA distinguishes magnetite compositions from the studied VMS deposits and BIFs from that of the other ore deposit types including Ni–Cu, porphyry Cu-Mo-Au, iron oxide-copper- gold, iron oxide-apatite, and the Bayan Obo REE-Fe-Nb deposit. Magnetite from the VMS settings on average contains lower concentrations of Si, Zr, Al, Mg, Ti, Zn, Co and Ni relative to that from the other mineral deposit types. PLS-DA of magnetite data from VMS deposits and BIFs of the Bathurst mining camp as well as PLS-DA of magnetite compositions from various mineral deposit types yield discrimination models for application to mineral exploration for VMS deposits using indicator minerals in Quaternary lithified sedimentary rocks.  相似文献   

3.
玻利维亚的铜矿规模以中小型为主,主要成矿类型为红层型(砂岩层)、沉积相关脉状型、VMS型和IOCG型等。金矿规模以中小型为主,主要成矿类型有火山成因浅成热液型、与深成岩相关的脉状矿床、造山型矿床和砂金矿。锡矿发育众多大型、超大型矿床,成矿类型以玻利维亚型多金属脉状矿床和与长英质深成岩相关的脉状矿床为主,少量砂锡矿。铁矿以El Mutún超大型BIF型铁锰矿著称。西科迪勒拉和玻利维亚高原有重要的浅成低温热液贵金属资源潜力;东科迪勒拉北部主要为钨、锡、金、锑资源,中部为锡、银、金、锑资源,南部有金、锑、银、铅、锌潜力;次安第斯带南部有银-锌资源潜力;查科-贝尼平原带有广泛的砂金矿资源;前寒武纪克拉通内金、铂、镍、钽、铜和铁锰资源潜力丰富。  相似文献   

4.
The Bhukia gold (+copper) deposit hosted by albitite and carbonates that occur within the Paleoproterozoic Aravalli-Delhi Fold Belt (ADFB) in western India consists of magnetite, graphite, apatite and tourmaline along with sulfide mineralization. Ubiquitous presence of magnetite and apatite in gold-sulfide association, alteration patterns and shear controlled mineralization suggest it to be IOCG (Iron-oxide copper gold) type deposits. The detailed mineral chemistry of magnetite and apatite are generated and interpreted in terms of their genetic significance, hydrothermal and magmatic origin vis-à-vis their affiliation with IOCG deposition. The data suggest that the magnetite has hydrothermal affiliation. The Ni/Cr ratio is greater than 1, which is explained by differences in solubility and mobility of Ni and Cr in hydrothermal fluids and is corroborated with other key evidences including that of wide ranging Mg concentration further supports a strong hydrothermal input that is envisaged for the deposition of magnetite. Concentration of vanadium in magnetite is generally <1000 ppm in case of barren hydrothermal occurrences while in the study area, it is relatively higher as it is attributed to the gold-sulfide-Cu mineralization. Ti vs Ni/Cr, Ni/(Cr+Mn) vs Ti+V, Ca+Al+Mn vs Ti+V and Al+Mn vs Ti+V variations are interpreted in terms of magnetite genesis. EPMA data suggests that apatite present in Bhukia is of fluorapatite variety with F content >1 wt% and F/Cl >1. Higher concentration of F and moderate Mn along with lower concentration of Cl attests their magmatic hydrothermal character and its derivation from meta-volcano sedimentary source. REE patterns obtained from LA-ICP-MS analysis suggest enrichment of LREE relative to MREE and HREE with negative Eu anomaly. Y/∑REE, La/Sm, Ce/Th and Eu/Eu1 vs Ce/Ce1 values of apatite is indicative of their origin in a highly oxidized environment. Presence of magnetite along with apatite is a common feature in IOCG-IOA (Iron-Oxide Apatite) association. Bhukia Gold Deposit has many similarities with Kiruna type Iron-Oxide Apatite (IOA) deposits particularly with respect to their similar tectonic setting, alteration patterns, mineral assemblages such as abundance of magnetite, apatite and presence of late stage sulfides based on EPMA and Laser ablation ICP-MS (LA-ICP-MS) studies. Lithological, petro-mineralogical and geochemical signatures of magnetite and apatite infer that the Bhukia is a possible IOCG-IOA type gold deposit typically associated with sulfides and graphite which may be used as petrogenetic indicators and pathfinders for exploration.  相似文献   

5.
The origin of the hypersaline fluids (magmatic or basinal brine?), associated with iron oxide (Cu–U–Au–REE) deposits, is controversial. We report the first chlorine and strontium isotope data combined with Cl/Br ratios of fluid inclusions from selected iron oxide–copper–gold (IOCG) deposits (Candelaria, Raúl–Condestable, Sossego), a deposit considered to represent a magmatic end member of the IOCG class of deposit (Gameleira), and a magnetite–apatite deposit (El Romeral) from South America. Our data indicate mixing of a high δ 37Cl magmatic fluid with near 0‰ δ 37Cl basinal brines in the Candelaria, Raúl–Condestable, and Sossego IOCG deposits and leaching of a few weight percent of evaporites by magmatic-hydrothermal (?) fluids at Gameleira and El Romeral. The Sr isotopic composition of the inclusion fluids of Candelaria, Raúl–Condestable, and El Romeral confirms the presence of a non-magmatic fluid component in these deposits. The heavy chlorine isotope signatures of fluids from the IOCG deposits (Candelaria, Raúl–Condestable, Sossego), reflecting the magmatic-hydrothermal component of these fluids, contrast with the near 0‰ δ 37Cl values of porphyry copper fluids known from the literature. The heavy chlorine isotope compositions of fluids of the investigated IOCG deposits may indicate a prevailing mantle Cl component in contrast to porphyry copper fluids, an argument also supported by Os isotopes, or could result from differential Cl isotope fractionation processes (e.g. phase separation) in fluids of IOCG and porphyry Cu deposits.  相似文献   

6.
Magnetite is a common mineral in many ore deposits and their host rocks, and contains a wide range of trace elements (e.g., Ti, V, Mg, Cr, Mn, Ca, Al, Ni, Ga, Sn) that can be used for deposit type fingerprinting. In this study, we present new magnetite geochemical data for the Longqiao Fe deposit (Luzong ore district) and Tieshan Fe–(Cu) deposit (Edong ore district), which are important magmatic-hydrothermal deposits in eastern China.Textural features, mineral assemblages and paragenesis of the Longqiao and Tieshan ore samples have suggested the presence of two main mineralization periods (sedimentary and hydrothermal) at Longqiao, among which the hydrothermal period comprises four stages (skarn, magnetite, sulfide and carbonate); whilst the Tieshan Fe–(Cu) deposit comprises four mineralization stages (skarn, magnetite, quartz-sulfide and carbonate).Magnetite from the Longqiao and Tieshan deposits has different geochemistry, and can be clearly discriminated by the Sn vs. Ga, Ni vs. Cr, Ga vs. Al, Ni vs. Al, V vs. Ti, and Al vs. Mg diagrams. Such difference may be applied to distinguish other typical skarn (Tieshan) and multi-origin hydrothermal (Longqiao) deposits in the MLYRB. The fluid–rock interactions, influence of the co-crystallizing minerals and other physicochemical parameters, such as temperature and fO2, may have altogether controlled the magnetite trace element contents of both deposits. The Tieshan deposit may have had higher degree of fO2, but lower fluid–rock interactions and ore-forming temperature than the Longqiao deposit. The TiO2–Al2O3–(MgO + MnO) and (Ca + Al + Mn) vs. (Ti + V) magnetite discrimination diagrams show that the Longqiao Fe deposit has both sedimentary and hydrothermal features, whereas the Tieshan Fe–(Cu) deposit is skarn-type and was likely formed via hydrothermal metasomatism, consistent with the ore characteristics observed.  相似文献   

7.
The Marcona–Mina Justa deposit cluster, hosted by Lower Paleozoic metaclastic rocks and Middle Jurassic shallow marine andesites, incorporates the most important known magnetite mineralization in the Andes at Marcona (1.9 Gt at 55.4% Fe and 0.12% Cu) and one of the few major iron oxide–copper–gold (IOCG) deposits with economic Cu grades (346.6 Mt at 0.71% Cu, 3.8 g/t Ag and 0.03 g/t Au) at Mina Justa. The Middle Jurassic Marcona deposit is centred in Ica Department, Perú, and the Lower Cretaceous Mina Justa Cu (Ag, Au) prospect is located 3–4 km to the northeast. New fluid inclusion studies, including laser ablation time-of-flight inductively coupled plasma mass spectrometry (LA-TOF-ICPMS) analysis, integrated with sulphur, oxygen, hydrogen and carbon isotope analyses of minerals with well-defined paragenetic relationships, clarify the nature and origin of the hydrothermal fluid responsible for these contiguous but genetically contrasted deposits. At Marcona, early, sulphide-free stage M-III magnetite–biotite–calcic amphibole assemblages are inferred to have crystallized from a 700–800°C Fe oxide melt with a δ18O value from +5.2‰ to +7.7‰. Stage M-IV magnetite–phlogopite–calcic amphibole–sulphide assemblages were subsequently precipitated from 430–600°C aqueous fluids with dominantly magmatic isotopic compositions (δ34S = +0.8‰ to +5.9‰; δ18O = +9.6‰ to +12.2‰; δD = −73‰ to −43‰; and δ13C = −3.3‰). Stages M-III and M-IV account for over 95% of the magnetite mineralization at Marcona. Subsequent non-economic, lower temperature sulphide–calcite–amphibole assemblages (stage M-V) were deposited from fluids with similar δ34S (+1.8‰ to +5.0‰), δ18O (+10.1‰ to +12.5‰) and δ13C (−3.4‰), but higher δD values (average −8‰). Several groups of lower (<200°C, with a mode at 120°C) and higher temperature (>200°C) fluids can be recognized in the main polymetallic (Cu, Zn, Pb) sulphide stage M-V and may record the involvement of modified seawater. At Mina Justa, early magnetite–pyrite assemblages precipitated from a magmatic fluid (δ34S = +0.8‰ to +3.9‰; δ18O = +9.5‰ to +11.5‰) at 540–600°C, whereas ensuing chalcopyrite–bornite–digenite–chalcocite–hematite–calcite mineralization was the product of non-magmatic, probably evaporite-sourced, brines with δ34S ≥ +29‰, δ18O = 0.1‰ and δ13C = −8.3‰. Two groups of fluids were involved in the Cu mineralization stage: (1) Ca-rich, low-temperature (approx. 140°C) and high-salinity, plausibly a basinal brine and (2) Na (–K)-dominant with a low-temperature (approx. 140°C) and low-salinity probably meteoric water. LA-TOF-ICPMS analyses show that fluids at the magnetite–pyrite stage were Cu-barren, but that those associated with external fluids in later stages were enriched in Cu and Zn, suggesting such fluids could have been critical for the economic Cu mineralization in Andean IOCG deposits.  相似文献   

8.
Major Cu–Au deposits of iron oxide–copper–gold (IOCG) style are temporally associated with oxidized, potassic granitoids similar to those linked to major porphyry Cu–Au deposits. Stable and radiogenic isotope evidence indicates fluids and ore components were likely sourced from the intrusions. IOCG deposits form over a range of crustal levels because CO2-rich fluids separate from the magmas at higher pressures than in CO2-poor systems, thereby, promoting partitioning of H2O, Cl and metals to the fluid phase. At deep levels, the magma–fluid system cannot generate sufficient mechanical energy to fracture the host rocks as in porphyry systems and the IOCG deposits therefore form in a variety of fault-related structural traps where the magmatic fluids may mix with other fluids to promote ore formation. At shallow levels, the IOCG deposits form breccia and fracture-hosted mineralization styles similar to the hydrothermal intrusive breccias and sulphide vein systems that characterize many porphyry Cu–Au deposits. The fluids associated with IOCG deposits are typically H2O–CO2–salt fluids that evolve by unmixing of the carbonic phase and by mixing with fluids from other sources. In contrast, fluids in porphyry systems typically evolve by boiling of moderate salinity fluid to produce high salinity brine and a vapor phase commonly with input of externally derived fluids. These different fluid compositions and mechanisms of evolution lead to different alteration types and parageneses in porphyry and IOCG deposits. Porphyry Cu–Au deposits typically evolve through potassic, sericitic and (intermediate and/or advanced) argillic stages, while IOCG deposits typically evolve through sodic(–calcic), potassic and carbonate-rich stages, and at deeper levels, generally lack sericitic and argillic alteration. The common association of porphyry and IOCG Cu–Au deposits with potassic, oxidized intermediate to felsic granitoids, together with their contrasting fluid compositions, alteration styles and parageneses suggest that they should be considered as part of the broad family of intrusion-related systems but that they are typically not directly related to each other.  相似文献   

9.
Numerous Fe–Cu deposits are hosted in the late Paleoproterozoic Dongchuan and Dahongshan Groups in the Kangdian region, SW China. The Dongchuan Group is composed of siltstone, slate, and dolostone with minor volcanic rocks, whereas the Dahongshan Group has undergone lower amphibolite facies metamorphism and consists of quartz mica-schist, albitite, quartzite, marble and amphibolite with local migmatite. Deposits in the Dongchuan Group are commonly localized in the cores of anticlines, in fault bends and intersections, and at lithological contacts. Orebodies are closely associated with breccias, which are locally derived from the host rocks. Fe-oxides (magnetite and/or hematite) and Cu-sulfides (chalcopyrite, bornite) form disseminated, vein-like and massive ores, and typically fill open spaces in the host rocks. The deposits have extensive albite alteration and local K-feldspar alteration overprinted by quartz, carbonate, sericite and chlorite. Deposits in the Dahongshan Group have orebodies sub-parellel to stratification and show crude stratal partitioning of metals. Fe-oxide ores occur as massive and/or banded replacements within the breccia pipes, whereas Cu-sulfide ores occur predominantly as disseminations and veinlets within mica schists and massive magnetite ores. Ore textures suggest that Cu-sulfides formed somewhat later than Fe-oxides, but are possibly within the same mineralization event. Both ore minerals predated regional Neoproterozoic metamorphism. Both orebodies and host rocks have undergone extensive alteration of albite, scapolite, amphibole, biotite, sericite and chlorite. Silica and carbonate alterations are also widespread. Ore-hosting strata have a LA-ICP-MS zircon U–Pb age of 1681 ± 13 Ma, and a dolerite dyke cutting the Fe-oxide orebodies has an age of 1659 ± 16 Ma. Thus, the mineralization age of the Dahongshan deposit is constrained at between the two. All ores from the two groups have high Fe and low Ti, with variable Cu contents. Locally they are rich in Mo, Co, V, and REE, but all are poor in Pb and Zn. Sulfides from the Fe–Cu deposits have δ34S values mostly in the range of +2 to +6 per mil, suggesting a mix of several sources due to large-scale leaching of the strata with the involvement of evaporites. Isotopic dating and field relationships suggest that these deposits formed in the late Paleoproterozoic. Ore textures, mineralogy and alteration characteristics are typical of IOCG-type deposits and thus define a major IOCG metallogenic province with significant implications for future exploration.  相似文献   

10.
The Igarapé Bahia Cu–Au deposit in the Carajás Province, Brazil, is hosted by steeply dipping metavolcano-sedimentary rocks of the Igarapé Bahia Group. This group consists of a low greenschist grade unit of the Archean (∼2,750 Ma) Itacaiúnas Supergroup, in which other important Cu–Au and iron ore deposits of the Carajás region are also hosted. The orebody at Igarapé Bahia is a fragmental rock unit situated between chloritized basalt, with associated hyaloclastite, banded iron formation (BIF), and chert in the footwall and mainly coarse- to fine-grained turbidites in the hanging wall. The fragmental rock unit is a nearly concordant, 2 km long and 30–250 m thick orebody made up of heterolithic, usually matrix-supported rocks composed mainly of coarse basalt, BIF, and chert clasts derived from the footwall unit. Mineralization is confined to the fine-grained matrix and comprises disseminated to massive chalcopyrite accompanied by magnetite, gold, U- and light rare earth element (LREE)-minerals, and minor other sulfides like bornite, molybdenite, cobaltite, digenite, and pyrite. Gangue minerals include siderite, chlorite, amphibole, tourmaline, quartz, stilpnomelane, epidote, and apatite. A less important mineralization style at Igarapé Bahia is represented by late quartz–chalcopyrite–calcite veins that crosscut all rocks in the deposit area. Fluid inclusions trapped in a quartz cavity in the ore unit indicate that saline aqueous fluids (5 to 45 wt% NaCl + CaCl2 equiv), together with carbonic (CO2 ± CH4) and low-salinity aqueous carbonic (6 wt% NaCl equiv) fluids, were involved in the mineralization process. Carbonates from the fragmental layer have δ13C values from −6.7 to −13.4 per mil that indicate their origin from organic and possibly also from magmatic carbon. The δ34S values for chalcopyrite range from −1.1 to 5.6 per mil with an outlier at −10.8 per mil, implying that most sulfur is magmatic or leached from magmatic rocks, whereas a limited contribution of reduced and oxydized sulfur is also evident. Oxygen isotopic ratios in magnetite, quartz, and siderite yield calculated temperatures of ∼400°C and δ18O-enriched compositions (5 to 16.5 per mil) for the ore-forming fluids that suggest a magmatic input and/or an interaction with 18O-rich, probably sedimentary rocks. The late veins of the Igarapé Bahia deposit area were formed from saline aqueous fluids (2 to 60 wt% NaCl + CaCl2 equiv) with δ18Ofluid compositions around 0 per mil that indicate contribution from meteoric fluids. With respect to geological features, Igarapé Bahia bears similarity with syngenetic, volcanic-hosted massive sulfide (VHMS)-type deposits, as indicated by the volcano-sedimentary geological context, stratabound character, and association with submarine volcanic flows, hyaloclastite, and exhalative beds such as BIF and chert. On the other hand, the highly saline ore fluids and the mineral assemblage, dominated by magnetite and chalcopyrite, with associated gold, U- and LREE-minerals and scarce pyrite, indicate that Igarapé Bahia belongs to the Fe oxide Cu–Au (IOCG) group of deposits. The available geochronologic data used to attest syngenetic or epigenetic origins for the mineralization are either imprecise or may not represent the main mineralization episode but a later, superimposed event. The C, S, and O isotopic results obtained in this study do not clearly discriminate between fluid sources. However, recent B isotope data obtained on tourmaline from the matrix of the fragmental rock ore unit (Xavier, Wiedenbeck, Dreher, Rhede, Monteiro, Araújo, Chemical and boron isotopic composition of tourmaline from Archean and Paleoproterozoic Cu–Au deposits in the Carajás Mineral Province, 1° Simpósio Brasileiro de Metalogenia, Gramado, Brazil, extended abstracts, CD-ROM, 2005) provide strong evidence of the involvement of a marine evaporitic source in the hydrothermal system of Igarapé Bahia. Evaporite-derived fluids may explain the high salinities and the low reduced sulfur mineral paragenesis observed in the deposit. Evaporite-derived fluids also exclude a significant participation of magmatic or mantle-derived fluids, reinforcing the role of nonmagmatic brines in the genesis of Igarapé Bahia. Considering this aspect and the geological features, the possibility that the deposit was generated by a hydrothermal submarine system whose elevated salinity was acquired by leaching of ancient evaporite beds should be evaluated.  相似文献   

11.
The Beiya gold–polymetallic deposit is one of the largest gold deposits in China and is considered to be a typical porphyry-skarn system located in the middle of the Jinshajiang–Ailaoshan alkaline porphyry metallogenic belt. Massive magnetite is widespread in the Beiya ore district but its genesis is still the subject of debate. Five representative magnetite types are present in the Beiya deposit, namely magmatic magnetite (M1) from the ore-related porphyry, disseminated magnetite (M2) from the early retrograde alteration, massive magnetite (M3) from the early quartz-magnetite stage, massive magnetite (M4) from the middle quartz-magnetite stage and magnetite (M5) from the late quartz-magnetite stage. Compared with the M1 magnetite, the magnetites from stages M2 to M5 are depleted in Ti, Al and high field strength elements, implying a hydrothermal origin, distinct from the magmatic accessory magnetite in the ore-related porphyry (M1). The concentrations of cobalt in the hydrothermal magnetites decrease gradually from M2 to M5, and can be used to discriminate the magnetite types. The Al + Mn and Ti + V contents of the successively precipitated magnetite grains (M2–M5) suggests that the ore forming temperature decreased from M2 to M4, but increased from M4 to M5, possibly as the result of a new pulse of magma entering the chamber, which may have triggered the gold mineralization. The V content in the hydrothermal magnetite suggests that the oxygen fugacity increased from M2 to M4 but decreased as soon as the sulfides entered the system (M5).  相似文献   

12.
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.  相似文献   

13.
The Lamandau region of Kalimantan Island, Indonesia is located in Sandaland, in the southern part of the Kuching tectonic belt. A series of Cenozoic epithermal gold deposits and Fe–Cu–Au deposits are located in the Kuching belt. The Lamandau Fe–Cu–Au deposit is hosted by diorite porphyry. In-situ zircon U–Pb dating of the diorite porphyry shows that it formed between 82.1 ± 1.7 Ma and 78.7 ± 2.3 Ma. Geochemical data indicate a depletion of high field strength elements (HFSE) in the diorite porphyry and related basalt is similar to that of arc-related igneous rocks. The diorite porphyry and basalt were probably derived from typical arc magmas related to continental margin subduction and thus are characterized by light rare earth element (REE) enrichment and HFSE depletion. The sub-chondritic Nb/Ta ratios for the basalt in the Lamandau region indicate that the subducted Pacific slab began partial melting at depths where amphibole was the major residual phase, with some residual rutile. The basalt was derived from a depleted mantle source. The composition of apatite and zircon in the diorite porphyry indicates that the dioritic magma was produced from the subcontinental mantle after it was metasomatized by slab-derived fluids. The magma had a high oxygen fugacity, thus and therefore it was particularly conducive to the precipitation of Cu, Au and other ore-forming elements. The composition of magnetite indicates that it was of volcanic origin. The magnetite has a low REE content, and a high Cu–Au content. The deposit may be classified as an IOCG mineral system. In summary, the ore-related diorite porphyry in the Lamandau region might have formed in an extensional environment during rollback of the subducting western Pacific plate. The convergent velocity between the Philippine Sea and Eurasian plates was at a minimum during the rollback, so that the margin of East Asian began to undergo rifting with associated magmatism.  相似文献   

14.
“Magmato-Hydrothermal Space” is a new mathematical construct where 24 ore and pathfinder elements are used to quantify ore-element signatures. Quantification allows relationships between ore deposit samples to be mapped. The broad-scale view of Magmato-Hydrothermal Space reveals three important trends: (1) Zn-Pb sediment-hosted mineralisation to igneous-associated Cu-Au mineralisation, (2) Cu-Au mineralisation to Au-only mineralisation, and (3) ultramafic associated magmatic Ni-Cu-PGE mineralisation through Cu-Au mineralisation to granitoid-associated Mo, W and Sn mineralisation. The view provided by Magmato-Hydrothermal Space reveals that there is a spectrum of ore element signatures that mirrors the spectrum of ore deposit classes described in the literature.Geochemical variations within individual ore deposit classes are examined for orogenic-Au, VHMS, epithermal and sediment-hosted Cu samples. Sub-groups within each of these classes are compared on element enrichment diagrams and described in the context of Magmato-Hydrothermal Space. Orogenic Au samples are divided into two sub-groups of As-Sb rich mineralisation and four sub-groups of relatively As-Sb poor mineralisation. The As-Sb poor sub-groups include a Te-Cu-Ag rich sub-group that overlaps with the porphyry Cu class and a Te-W-(Bi-Mo) rich class dominated by granitoid hosted deposits. The VHMS class ranges from a Cu-rich sub-group that overlaps with porphyry Cu and IOCG classes through a Cu-Zn sub-group to two Zn-Cu sub-groups, one of which overlaps with the SHMS class. The epithermal class is divided into Zn-rich, Cu-rich and base metal – poor sub-groups.  相似文献   

15.
http://www.sciencedirect.com/science/article/pii/S1674987114000711   总被引:1,自引:0,他引:1  
The West Junggar region,located in the loci of the Central Asian Orogenic Belt,is a highly endowed metallogenic province with >100 tonnes Au,>0.7 Mt Cu,>0.3 Mt Mo,and >2.3 Mt chromite as well as significant amounts of Be and U.The West Junggar region has three metallogenic belts distributed systematically from north to south:(1) late Paleozoic Saur Au-Cu belt;(2) early Paleozoic XiemisitaiSharburt Be-U-Cu-Zn belt;(3) late Paleozoic Barluk-Kelamay Au-Cu-Mo-Cr belt.These belts host a number of deposits belonging to at least eight economically important styles,including epithermal Au,granite-related Be-U,volcanogenic massive sulfide(VMS) Cu-Zn,podiform chromite,porphyry Cu,hydrothermal quartz vein Au,porphyry-greisen Mo(-W),and orogenic Au.These deposit styles are associated with the tectonics prevalent during their formation.Five tectonic-mineralized epochs can be recognized:(1) Ordovician subduction-related VMS Cu-Zn deposit;(2) Devonian ophiolite-related podiform chromite deposit;(3) early Carboniferous subduction-related epithermal Au and porphyry Cu deposits;(4) late Carboniferous subduction-related granite-related Be-U,porphyry Cu,and hydrothermal quartz vein Au deposits;and(5) late Carboniferous to early Permian subduction-related porphyry-greisen Mo(-W) and orogenic Au deposits.  相似文献   

16.
In southwestern China, several large magmatic Fe–Ti–V oxide ore deposits are hosted by gabbroic intrusions associated with the Emeishan flood basalts. The Panzhihua gabbroic intrusion, a little deformed sill that contains a large titanomagnetite deposit at its base, concordantly intrudes late-Proterozoic dolostones. Mineralogical and chemical studies of the contact aureole in the footwall dolostones demonstrate that the metamorphism was largely isochemical but released large quantities of CO2 as the rocks were converted to marble and skarns during intrusion of the gabbroic magma. Petrological modelling of the crystallization of the intrusion, using H2O-poor Emeishan basalt as parent magma, shows that under normal conditions, Fe–Ti oxides crystallize at a late stage, after the crystallization of abundant olivine, clinopyroxene and plagioclase. In order for titanomagnetite to separate efficiently to form the ore deposit, this mineral must have crystallized earlier and close to the liquidus. We propose that CO2-rich fluids released during decarbonatization of sedimentary floor rocks passed up through the magma. Redox equilibria calculations show that when magma with the composition of Emeishan basalt is fluxed by a CO2-rich gas phase, its equilibrium oxygen fugacity (fO2) increases from the fayalite–magnetite–quartz buffer (FMQ) to FMQ + 1.5. From experimental constraints on magnetite saturation in basaltic magma under controlled fO2, such an oxidizing event would allow magnetite to crystallize near to the liquidus, leading to the formation of the deposit.  相似文献   

17.
智利科皮亚波GV地区侵入岩地球化学及年代学研究   总被引:3,自引:2,他引:1  
智利北中部科皮亚波GV地区位于中生代铁氧化物铜金(IOCG)矿床与斑岩铜矿过渡带。侵入岩体主要为辉长闪长岩、闪长岩、闪长斑岩、黑云母花岗岩、斑状花岗岩和二长岩。岩石地球化学特征说明该侵入岩体属于钙碱性、I型或磁铁矿系列,来源于深部上地幔。推测这些岩浆岩岩石组合形成于洋壳俯冲带,局部扩张与挤压转换导致弧后盆地萎缩封闭并快速抬升。岩浆侵入具有多期次活动,形成了多期次热液活动中心,并发育面型与脉带型蚀变矿化分带,地表具有寻找大型IOCG矿床前景。地表泥化-绿泥石-多孔状硅化网脉和含金银多金属铁锰碳酸盐化网脉发育,含金银多金属网脉状-带状和面型蚀变区揭示地表有浅成低温热液型金银多金属矿床;深部具有寻找隐伏斑岩型铜金矿床前景。今后需在该区加强蚀变矿化分带规律研究,进行深部找矿预测。  相似文献   

18.
前寒武纪VMS与BIF铁矿床共生组合研究进展   总被引:1,自引:1,他引:0  
VMS和BIF铁矿作为两种重要的矿床类型,在前寒武纪常常以共生组合方式赋存于古老克拉通内的表壳岩系中,是早期地球构造和环境演化耦合作用的产物。该组合不仅记录了当时特定的构造及大气和海洋环境,而且两者也是全球铜、铁、铅、锌等金属的重要来源,因此,开展VMS与BIF共生组合的研究具有重大科学价值和经济意义。前人研究表明,前寒武纪VMS与BIF集中出现于~2.7 Ga和~1.9 Ga,与同时期地幔柱活动和地壳增生的高峰相对应,两者共生时BIF通常产出于VMS外围或上盘,但在矿体空间展布上具有此消彼长的关系;研究还认为,前寒武纪地幔柱活动诱发的海底扩张、海底和地表强烈的火山活动形成的多重热液系统,可同时为VMS和BIF提供物质来源,海水的硫逸度、氧逸度及大气的氧含量是影响VMS与BIF空间分布及VMS硫同位素组成的重要因素。目前,VMS与BIF共生组合研究取得了较大进展,但仍存在一些问题:缺乏典型共生实例的精细解剖,已有共生模型缺乏详细的矿床成因机制研究支撑,对两者共生组合产出的构造背景和古海洋环境仍存在不同认识。华北克拉通的清原和五台新太古代绿岩带发育有较大规模的VMS与BIF铁矿共生现象,对其开展详细研究工作将为解决上述问题提供借鉴。  相似文献   

19.
In western Peru kaolin-alunite deposits occur in Lower Cretaceous and Tertiary clastic, volcaniclastic and volcanic, mostly rhyolitic, rocks. Alunites from␣hypogene kaolin deposits yield  K /Ar ages of 11.5 ±␣0.7␣Ma and 13.3 ± 0.4 Ma. In addition to kaolin and alunite, the following minerals are present: white mica, smectite, barite, pyrophyllite, tridymite, cristobalite, α- and β-quartz, chamosite, gibbsite, and aluminum-phosphate-sulphate minerals (APS). APS mineralizations with REE-bearing svanbergite and florencite originate from supergene alteration. Woodhouseite, goyazite, crandallite and pure svanbergite develop in hypogene and supergene kaolin deposits. The distinction between hypogene and supergene kaolinization can be made using various element ratios in kaolin (P vs. S, Zr vs. Ti, Cr + Nb vs. Ti + Fe, and Ce + Y + La vs. Ba + Sr). S,␣Ba, and Sr are considerably enriched in kaolin during hydrothermal alteration, whereas Cr, Nb, Ti and lanthanide elements are concentrated mainly during weathering. Au and Ag become enriched during hypogene kaolinization (advanced argillitization). Kaolinization is associated with the evolution of the Central Andes as follows: (1) during the Lower Cretaceous kaolinization characterizes phases of relative tectonic quiescence during mountain building and took place in a miogeosynclinal back-arc basin. The kaolin-bearing sediments were laid down in flood plain to delta plain environments; (2) in the magmatic arc/back-arc basin (eugeosyncline) kaolinization was mainly associated with uplift and peneplanation; (3) in the magmatic arc proper, late Miocene kaolinization of volcanic and volcaniclastic rocks has many features in common with the high sulphidation epithermal Au deposits. Received: 11 August 1995 / Accepted: 8 May 1996  相似文献   

20.
The Antucoya porphyry copper deposit (300 Mt at 0.45% total Cu) is one of the largest deposits of a poorly known Early Cretaceous porphyry belt in the Coastal Cordillera of northern Chile. It is related to a succession of granodioritic and tonalitic porphyritic stocks and dikes that were emplaced within Jurassic andesitic rocks of the La Negra Formation immediately west of the N–S trending sinistral strike-slip Atacama Fault Zone. New zircon SHRIMP U–Pb data indicate that the porphyries of Antucoya crystallized within the time span from 142.7 ± 1.6 to 140.6 ± 1.5 Ma (±2 σ), and late, unmineralized, NW–SE trending dacite dikes with potassic alteration and internal deformation crystallized at 141.9 ± 1.4 Ma. The Antucoya porphyry copper system appears to be formed after a change of stress conditions along the magmatic arc from extensional in the Late Jurassic to transpressive during the Early Cretaceous and provides support for an Early Cretaceous metallogenic episode of porphyry-type mineralization along the Coastal Cordillera of northern Chile.  相似文献   

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