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1

Anand, Abhishek, Sahendra Singh, Arindam Gantait, Amit Srivastava, Girish Kumar Mayachar, and Manoj Kumar. "Geological Constraints on the Genesis of Jagpura Au-Cu Deposit NW India: Implications from Magnetite-Apatite Mineral Chemistry, Fluid Inclusion and Sulfur Isotope Study." Minerals 12, no. 11 (October 24, 2022): 1345. http://dx.doi.org/10.3390/min12111345.

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The Jagpura Au-Cu deposit is situated within the Aravalli craton in the northwestern part of India. In the present work, petrography, mineral chemistry, fluid inclusion and sulfur isotopic compositions were used to study the Jagpura Au-Cu deposit. The ore mineral association of the deposit is arsenopyrite, loellingite, chalcopyrite, pyrrhotite and pyrite, along with native gold, magnetite and apatite. The gold fineness ranges from 914–937‰ (avg. 927‰). The presence of Au-Bi-Te phases, pyrite (>1 Co/Ni ratio), magnetite (≥1 Ni/Cr ratio, <1 Co/Ni ratio) and apatite (>1 F/Cl ratio) suggest the hydrothermal origin Au-Cu mineralization. A fluid inclusion study indicates the different episodes of fluid immiscibility with the homogenization temperatures varying between 120–258 °C and salinities range within the 8.86–28.15 wt% NaCl eq. The sulfur isotopic composition of sulfides varies from 8.98 to 14.58‰ (avg. 11.16‰). It is inferred that the variation in the sulfur isotopic compositions of sulfides is due to the cooling and dilution of the metalliferous fluid of mixed origin, derived from the basement meta-sedimentary rocks and the high saline basinal fluid. The iron oxide-copper-gold-apatite associations, structural control of mineralization, pervasive hydrothermal alteration, fluid salinity and sulfur isotope compositions indicate that the Jagpura Au-Cu deposit is similar to the iron oxide-copper-gold (IOCG)-iron oxide-apatite (IOA)types of deposits. Based on the ore geochemistry and the trace elements systematic of magnetite, the deposit is further classified as an IOCG-IOA type: IOCG-Co (reduced) subtype.
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2

Reid, Anthony. "The Olympic Cu-Au Province, Gawler Craton: A Review of the Lithospheric Architecture, Geodynamic Setting, Alteration Systems, Cover Successions and Prospectivity." Minerals 9, no. 6 (June 20, 2019): 371. http://dx.doi.org/10.3390/min9060371.

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The Olympic Cu-Au Province is a metallogenic province in South Australia that contains one of the world’s most significant Cu-Au-U resources in the Olympic Dam deposit. The Olympic Cu-Au Province also hosts a range of other iron oxide-copper-gold (IOCG) deposits including Prominent Hill and Carrapateena. This paper reviews the geology of the Olympic Cu-Au Province by investigating the lithospheric architecture, geodynamic setting and alteration systematics. In addition, since the province is almost entirely buried by post-mineral cover, the sedimentary cover sequences are also reviewed. The Olympic Cu-Au Province formed during the early Mesoproterozoic, ca. 1.6 Ga and is co-located with a fundamental lithospheric boundary in the eastern Gawler Craton. This metallogenic event was driven in part by melting of a fertile, metasomatized sub-continental lithospheric mantle during a major regional tectonothermal event. Fluid evolution and multiple fluid mixing resulted in alteration assemblages that range from albite, magnetite and other higher temperature minerals to lower temperature assemblages such as hematite, sericite and chlorite. IOCG mineralisation is associated with both high and low temperature assemblages, however, hematite-rich IOCGs are the most economically significant. Burial by Mesoproterzoic and Neoproterozoic-Cambrian sedimentary successions preserved the Olympic Cu-Au Province from erosion, while also providing a challenge for mineral exploration in the region. Mineral potential modelling identifies regions within the Olympic Cu-Au Province and adjacent Curnamona Province that have high prospects for future IOCG discoveries. Exploration success will rely on improvements in existing potential field and geochemical data, and be bolstered by new 3D magnetotelluric surveys. However, drilling remains the final method for discovery of new mineral resources.
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3

Rodriguez-Mustafa, Maria A., Adam C. Simon, Irene del Real, John F. H. Thompson, Laura D. Bilenker, Fernando Barra, Ilya Bindeman, and David Cadwell. "A Continuum from Iron Oxide Copper-Gold to Iron Oxide-Apatite Deposits: Evidence from Fe and O Stable Isotopes and Trace Element Chemistry of Magnetite." Economic Geology 115, no. 7 (November 1, 2020): 1443–59. http://dx.doi.org/10.5382/econgeo.4752.

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Abstract Iron oxide copper-gold (IOCG) and iron oxide-apatite (IOA) deposits are major sources of Fe, Cu, and Au. Magnetite is the modally dominant and commodity mineral in IOA deposits, whereas magnetite and hematite are predominant in IOCG deposits, with copper sulfides being the primary commodity minerals. It is generally accepted that IOCG deposits formed by hydrothermal processes, but there is a lack of consensus for the source of the ore fluid(s). There are multiple competing hypotheses for the formation of IOA deposits, with models that range from purely magmatic to purely hydrothermal. In the Chilean iron belt, the spatial and temporal association of IOCG and IOA deposits has led to the hypothesis that IOA and IOCG deposits are genetically connected, where S-Cu-Au–poor magnetite-dominated IOA deposits represent the stratigraphically deeper levels of S-Cu-Au–rich magnetite- and hematite-dominated IOCG deposits. Here we report minor element and Fe and O stable isotope abundances for magnetite and H stable isotope abundances for actinolite from the Candelaria IOCG deposit and Quince IOA prospect in the Chilean iron belt. Backscattered electron imaging reveals textures of igneous and magmatic-hydrothermal affinities and the exsolution of Mn-rich ilmenite from magnetite in Quince and deep levels of Candelaria (&gt;500 m below the bottom of the open pit). Trace element concentrations in magnetite systematically increase with depth in both deposits and decrease from core to rim within magnetite grains in shallow samples from Candelaria. These results are consistent with a cooling trend for magnetite growth from deep to shallow levels in both systems. Iron isotope compositions of magnetite range from δ56Fe values of 0.11 ± 0.07 to 0.16 ± 0.05‰ for Quince and between 0.16 ± 0.03 and 0.42 ± 0.04‰ for Candelaria. Oxygen isotope compositions of magnetite range from δ18O values of 2.65 ± 0.07 to 3.33 ± 0.07‰ for Quince and between 1.16 ± 0.07 and 7.80 ± 0.07‰ for Candelaria. For cogenetic actinolite, δD values range from –41.7 ± 2.10 to –39.0 ± 2.10‰ for Quince and from –93.9 ± 2.10 to –54.0 ± 2.10‰ for Candelaria, and δ18O values range between 5.89 ± 0.23 and 6.02 ± 0.23‰ for Quince and between 7.50 ± 0.23 and 7.69 ± 0.23‰ for Candelaria. The paired Fe and O isotope compositions of magnetite and the H isotope signature of actinolite fingerprint a magmatic source reservoir for ore fluids at Candelaria and Quince. Temperature estimates from O isotope thermometry and Fe# of actinolite (Fe# = [molar Fe]/([molar Fe] + [molar Mg])) are consistent with high-temperature mineralization (600°–860°C). The reintegrated composition of primary Ti-rich magnetite is consistent with igneous magnetite and supports magmatic conditions for the formation of magnetite in the Quince prospect and the deep portion of the Candelaria deposit. The trace element variations and zonation in magnetite from shallower levels of Candelaria are consistent with magnetite growth from a cooling magmatic-hydrothermal fluid. The combined chemical and textural data are consistent with a combined igneous and magmatic-hydrothermal origin for Quince and Candelaria, where the deeper portion of Candelaria corresponds to a transitional phase between the shallower IOCG deposit and a deeper IOA system analogous to the Quince IOA prospect, providing evidence for a continuum between both deposit types.
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4

Kostin, Aleksey. "Iron Oxide Cu-Au (IOCG) Mineralizing Systems: The Eastern Yakutia (Russia) Perspective." IOP Conference Series: Earth and Environmental Science 609 (December 16, 2020): 012005. http://dx.doi.org/10.1088/1755-1315/609/1/012005.

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5

Sillitoe, Richard H., Georgi Magaranov, Veselin Mladenov, and Robert A. Creaser. "ROSEN, BULGARIA: A NEWLY RECOGNIZED IRON OXIDE-COPPER-GOLD DISTRICT." Economic Geology 115, no. 3 (May 1, 2020): 481–88. http://dx.doi.org/10.5382/econgeo.4731.

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Abstract The Rosen copper veins in southeastern Bulgaria are recognized for the first time as an iron oxide-copper-gold (IOCG) district. The veins are located in the East Srednogorie segment of the Carpathian-Balkan calc-alkaline volcano-plutonic arc and were formed during an end-stage interval of extreme slab rollback and intra-arc rifting, which gave rise farther east to seafloor spreading in the Western Black Sea basin. The resulting submarine volcano-sedimentary rift basin is dominated by intermediate to mafic shoshonitic to ultrapotassic volcanism and subsidiary gabbro to syenite intrusion. The E- to NE-striking veins define a NW-striking alignment along the western contact of the syenite-dominated Rosen pluton, inferred to be part of a large ring dike. More than 40 veins, the most important formerly mined to depths as great as 1,000 m, contain an early, pegmatoidal, calcic-potassic assemblage followed by predominant magnetite (including the mushketovite variety), chlorite, and carbonates but also quartz, chalcopyrite, pyrite, and numerous other metallic minerals, which combine to give an unusual Fe-Cu-Au-Mo-Co-Ni-U-light rare earth element (LREE)-W-Bi-Zn-Pb geochemical signature. The close correlation between Fe, Cu, U, and LREEs is evident even in the flotation tailings. Vein molybdenite was dated during this study at 80.6 ± 0.4 Ma, which is similar to a U-Pb zircon age for monzosyenite from the Rosen pluton. The mineralogic and compositional features of the Rosen district are comparable to those of well-known IOCG deposits worldwide and geometrically similar to the vertically extensive IOCG veins in the Coastal Cordillera province of northern Chile. The subsidiary granitophile signature that accompanies the characteristic siderophile IOCG suite was also recognized recently at the giant Olympic Dam deposit in South Australia and elsewhere. Although no exposed intrusion is definitively implicated in the genesis of the Rosen veins, coexisting gabbro and syenite fluid sources may be hypothesized at depth in or beneath the coeval ring dike.
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6

Kostin, Aleksey. "A new mineral assemblage from the diorite complex in the Fe-Oxide-Cu-Au ores of the Kis-Kuel deposit (Eastern Yakutia, Russia)." IOP Conference Series: Earth and Environmental Science 906, no. 1 (November 1, 2021): 012007. http://dx.doi.org/10.1088/1755-1315/906/1/012007.

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Abstract This research continues our investigations of the iron-oxide copper-gold deposits in the Western Verkhoyansk region, where recent years efforts of the IGABM SB RAS led to the discovery of a new gold Kiskuel deposit. The Kis-Kuel intrusion-related IOCG deposit in Eastern Yakutia (Russia) with a wide range of mineral styles has a direct genetic link with a cooling intrusion during its formation. The IOCG worldwide and the Kis-Kuel deposit have common features for this style - the abundance of iron oxides and low of sulfides. Magmatic contribution to the Kis-Kuel deposit is significant. Intrusive rocks range from diorite to granodiorite in composition. The Kiskuel deposit hosted in diorites and granodiorites; xenoliths confirming deep mineralization represented by pyrrhotite (main), pyrite, chalcopyrite, and clinosafflorite (Co, Fe, Ni)As2, chromite, pentlandite. Clinosafflorite localized at the contact of pyrrhotite and chalcopyrite and at the contact of pyrrhotite and biotite. Chalcopyrite is found in intergrowth with pyrrhotite, were it forms bands and lenses. Parallel to the biotite cleavage, the thinnest layers of chalcopyrite are common. Clinosafflorite is rare and discovered in hydrothermal cobalt-nickel ores of the Bou-Azzer (Morocco), Cobalt (Canada), Glassberg (Germany), Silver Mine (England) and several others. Mineralization of rich mica processes occur in connection with the chromite, pentlandite, chalcopyrite, pyrite, and pyrrhotite; a common feature of the mineralized dark-colored rock is phlogopite abundance, ilmenite, potassium feldspar, calcite, rarely quartz; clinoenstatite metasomaticaly replaced with phlogopite and dolomite. This new evidence supports a magmatic-hydrothermal model for the formation of IOCG deposit in the Kis-Kuel, where iron-oxide mineralization sourced from intermediate magmas. The deep complex predominantly composed of chromite, ilmenite, magnetite, pentlandite, and clinocafflorite; less of galena and sphalerite. Many diverse mineraization systems from Kis-Kuel classified together as iron oxide copper-gold (IOCG) deposits. The obtained data suggest deep ore-bearing structure of the Kis-Kuel ore-magmatic cluster with the potential for discovering of a new mineral ores style. All of this help in developing a new robust prospecting model.
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7

Austin, James R., Phillip W. Schmidt, and Clive A. Foss. "Magnetic modeling of iron oxide copper-gold mineralization constrained by 3D multiscale integration of petrophysical and geochemical data: Cloncurry District, Australia." Interpretation 1, no. 1 (August 1, 2013): T63—T84. http://dx.doi.org/10.1190/int-2013-0005.1.

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Magnetite-rich iron oxide copper-gold deposits (IOCGs) are geologically and geochemically complex and present major challenges to geophysical investigation. They often sit beneath significant cover, exhibit magnetic remanence, and suffer from self-demagnetization effects. Because remanence in magnetite-bearing drill core samples is commonly overprinted by drilling, in situ natural remanent magnetization is difficult to measure accurately, and thus IOCGs cannot be modeled definitively using geophysics alone. We examined structural controls on a magnetite-rich IOCG in northwest Queensland and the relationships between structure, alteration, Fe oxides, and mineralization at core to deposit scale. Magnetite within the deposit has a multidomain structure, and thus it would commonly have an in situ magnetization parallel to the earth’s field. In contrast, pyrrhotite has a pseudosingle-domain structure and so it is the predominant carrier of stable remanence within the ore system. Geophysical lineament analyses are used to determine structural controls on mineralization, geophysical filters (e.g., analytic signal amplitude) are used to help define structural extent of the deposit, and basement geochemistry is used to map mineral footprints beneath cover. These techniques identified coincident anomalies at the intersection of north and northwest lineaments. Leapfrog™ interpolations of downhole magnetic susceptibility and Cu, Au, and Fe assay data were used to map the distribution of magnetite, copper, gold, and sulfur in 3D. The analysis revealed that Cu and Au mineralization were coupled with the magnetite net-vein architecture, but that Cu was locally enriched in the east–northeast-trending demagnetized zone. The results from this suite of geophysical, petrophysical, and geochemical techniques were integrated to constrain modeling of the Brumby IOCG. Brumby can be described as a breccia pipe sitting at the intersection of north-striking, east-dipping, and northwest-striking, southeast-dipping structures that plunges moderately to the south–southeast. The breccia pipe was overprinted by a relatively late net-vein magnetite breccia and crosscut by a later, magnetite-destructive, east–northeast-striking fault.
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8

Berdnikov, Nikolai, Victor Nevstruev, Pavel Kepezhinskas, Ivan Astapov, and Natalia Konovalova. "Gold in Mineralized Volcanic Systems from the Lesser Khingan Range (Russian Far East): Textural Types, Composition and Possible Origins." Geosciences 11, no. 2 (February 20, 2021): 103. http://dx.doi.org/10.3390/geosciences11020103.

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While gold partitioning into hydrothermal fluids responsible for the formation of porphyry and epithermal deposits is currently well understood, its behavior during the differentiation of metal-rich silicate melts is still subject of an intense scientific debate. Typically, gold is scavenged into sulfides during crustal fractionation of sulfur-rich mafic to intermediate magmas and development of native forms and alloys of this important precious metal in igneous rocks and associated ores are still poorly documented. We present new data on gold (Cu-Ag-Au, Ni-Cu-Zn-Ag-Au, Ti-Cu-Ag-Au, Ag-Au) alloys from iron oxide deposits in the Lesser Khingan Range (LKR) of the Russian Far East. Gold alloy particles are from 10 to 100 µm in size and irregular to spherical in shape. Gold spherules were formed through silicate-metal liquid immiscibility and then injected into fissures surrounding the ascending melt column, or emplaced through a volcanic eruption. Presence of globular (occasionally with meniscus-like textures) Cu-O micro-inclusions in Cu-Ag-Au spherules confirms their crystallization from a metal melt via extremely fast cooling. Irregularly shaped Cu-Ag-Au particles were formed through hydrothermal alteration of gold-bearing volcanic rocks and ores. Association of primarily liquid Cu-Ag-Au spherules with iron-oxide mineralization in the LKR indicates possible involvement of silicate-metallic immiscibility and explosive volcanism in the formation of the Andean-type iron oxide gold-copper (IOCG) and related copper-gold porphyry deposits in the deeper parts of sub-volcanic epithermal systems. Thus, formation of gold alloys in deep roots of arc volcanoes may serve as a precursor and an exploration guide for high-grade epithermal gold mineralization at shallow structural levels of hydrothermal-volcanic environments in subduction zones.
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9

Rodriguez-Mustafa, Maria A., Adam C. Simon, Laura D. Bilenker, Ilya Bindeman, Ryan Mathur, and Edson L. B. Machado. "The Mina Justa Iron Oxide Copper-Gold (IOCG) Deposit, Peru: Constraints on Metal and Ore Fluid Sources." Economic Geology 117, no. 3 (May 1, 2022): 645–66. http://dx.doi.org/10.5382/econgeo.4875.

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Abstract Iron oxide copper-gold (IOCG) deposits are major sources of Cu, contain abundant Fe oxides, and may contain Au, Ag, Co, rare earth elements (REEs), U, and other metals as economically important byproducts in some deposits. They form by hydrothermal processes, but the source of the metals and ore fluid(s) is still debated. We investigated the geochemistry of magnetite from the hydrothermal unit and manto orebodies at the Mina Justa IOCG deposit in Peru to assess the source of the iron oxides and their relationship with the economic Cu mineralization. We identified three types of magnetite: magnetite with inclusions (type I) is only found in the manto, is the richest in trace elements, and crystallized between 459° and 707°C; type Dark (D) has no visible inclusions and formed at around 543°C; and type Bright (B) has no inclusions, has the highest Fe content, and formed at around 443°C. Temperatures were estimated using the Mg content in magnetite. Magnetite samples from Mina Justa yielded an average δ56Fe ± 2σ value of 0.28 ± 0.05‰ (n = 9), an average δ18O ± 2σ value of 2.19 ± 0.45‰ (n = 9), and Δ’17O values that range between –0.075 and –0.047‰. Sulfide separates yielded δ65Cu values that range from –0.32 to –0.09‰. The trace element compositions and textures of magnetite, along with temperature estimations for magnetite crystallization, are consistent with the manto magnetite belonging to an iron oxide-apatite (IOA) style mineralization that was overprinted by a younger, structurally controlled IOCG event that formed the hydrothermal unit orebody. Altogether, the stable isotopic data fingerprint a magmatic-hydrothermal source for the ore fluids carrying the Fe and Cu at Mina Justa and preclude significant input from meteoric water and basinal brines.
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10

Logan, Leslie, Joel B. H. Andersson, Martin J. Whitehouse, Olof Martinsson, and Tobias E. Bauer. "Energy Drive for the Kiruna Mining District Mineral System(s): Insights from U-Pb Zircon Geochronology." Minerals 12, no. 7 (July 11, 2022): 875. http://dx.doi.org/10.3390/min12070875.

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The Kiruna mining district, Sweden, known for the type locality of Kiruna-type iron oxide–apatite (IOA) deposits, also hosts several Cu-mineralized deposits including iron oxide–copper–gold (IOCG), exhalative stratiform Cu-(Fe-Zn), and structurally controlled to stratabound Cu ± Au. However the relationship between the IOA and Cu-systems has not been contextualized within the regional tectonic evolution. A broader mineral systems approach is taken to assess the timing of energy drive(s) within a regional tectonic framework by conducting U-Pb zircon geochronology on intrusions from areas where Cu-mineralization is spatially proximal. Results unanimously yield U-Pb ages from the early Svecokarelian orogeny (ca. 1923–1867 Ma including age uncertainties), except one sample from the Archean basement (2698 ± 3 Ma), indicating that a distinct thermal drive from magmatic activity was prominent for the early orogenic phase. A weighted average 207Pb/206Pb age of 1877 ± 10 Ma of an iron-oxide-enriched gabbroic pluton overlaps in age with the Kiirunavaara IOA deposit and is suggested as a candidate for contributing mafic signatures to the IOA ore. The results leave the role of a late energy drive (and subsequent late Cu-mineralization and/or remobilization) ambiguous, despite evidence showing a late regional magmatic-style hydrothermal alteration is present in the district.
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11

Mehrabi, Behzad, Behrouz Karimishahraki, David Banks, Adrian Boyce, and Bruce W. D. Yardley. "Hydrothermal iron oxide-Cu-Au (IOCG) mineralization at the Jalal-Abad deposit, northwestern Zarand, Iran." Ore Geology Reviews 106 (March 2019): 300–317. http://dx.doi.org/10.1016/j.oregeorev.2019.01.019.

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12

Pollard, Peter J. "An intrusion-related origin for Cu–Au mineralization in iron oxide–copper–gold (IOCG) provinces." Mineralium Deposita 41, no. 2 (March 28, 2006): 179–87. http://dx.doi.org/10.1007/s00126-006-0054-x.

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13

Melo, Aline Tavares, Mônica Giannoccaro Von Huelsen, Umberto José Travaglia Filho, and Reinhardt Fuck. "A COMPARISON BETWEEN 1D ELECTROMAGNETIC MODELING PROGRAMS: A CASE HISTORY FOR CRISTALINO IRON OXIDE COPPER GOLD DEPOSIT, CARAJÁS MINERAL PROVINCE, BRAZIL." Revista Brasileira de Geofísica 32, no. 3 (September 1, 2014): 433. http://dx.doi.org/10.22564/rbgf.v32i3.501.

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ABSTRACT. Cristalino (482 Mt @ 0.65% Cu and 0.06 g/t Au) is a world class Cu-Au IOCG deposit located in the Carajás Mineral Province, Brazil. As extensiveoverburden cover makes exposure of the bedrock limited in Carajás region, geophysics plays a fundamental role in exploration. Detailed understanding of the geophysicalsignature of the known deposits is the key for future exploration as the targets are getting deeper. Two methods were applied to the 1D electromagnetic inversion (ImagEMand EM1DTM programs) and 2.5D plate modeling (Maxwell program). The inversion results for Cristalino show that even if the deposit is not massive sulfide, it waseffectively modeled and the methods respond very well to the ore body. The electromagnetic signature of the deposit obtained by the plate modeling is of 21S for thehigh-grade ore and 15S for the low-grade ore, and a new target was identified to the south of the main deposit. The anomalous body obtained by EM1DTM has theresistivity of 660 Ohm.m. Even though ImagEM is not quantitatively accurate, it can map the resistivity contrast with good precision.Keywords: electromagnetic modeling, Carajás, mineral exploration.RESUMO. Cristalino (482 Mt @ 0,65% Cu e 0,06 g/t Au), localizado na Província Mineral de Carajás, Brasil, é um depósito IOCG de Cu-Au de classe mundial.Como a extensa cobertura de solo limita a exposição de rocha não-intemperizada na região de Carajás, a geofísica se torna fundamental na exploração mineral. A compreensão detalhada da assinatura geofísica de depósitos conhecidos é a chave para o futuro da exploração, pois os alvos estão ficando cada vez mais profundos. Para este trabalho, dois métodos foram aplicados para a inversão eletromagnética 1D (programas ImagEM e EM1DTM) e modelo de placas 2,5D (programa Maxwell).Os resultados das inversões para Cristalino mostram que mesmo não sendo de sulfeto maciço, o depósito foi modelado de forma eficiente e que o método responde muito bem ao corpo de minério. A assinatura eletromagnética do depósito, obtida pelo modelo de placas, é de 21S para o minério de alto teor e 15S para o minério debaixo teor, e um novo alvo foi identificado a sul do depósito principal. O corpo anômalo obtido pelo EM1DTM tem resistividade de 660 Ohm.m. Mesmo que ImagEM não tenha acurácia quantitativa, pode mapear o contraste de resistividade com precisão muito boa.Palavras-chave: modelagem eletromagnética, Carajás, exploração mineral.
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14

Escolme, Angela, David R. Cooke, Julie Hunt, Ron F. Berry, Roland Maas, and Robert A. Creaser. "The Productora Cu-Au-Mo Deposit, Chile: A Mesozoic Magmatic-Hydrothermal Breccia Complex with Both Porphyry and Iron Oxide Cu-Au Affinities." Economic Geology 115, no. 3 (May 1, 2020): 543–80. http://dx.doi.org/10.5382/econgeo.4718.

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Abstract The Productora Cu-Au-Mo deposit is hosted by a Cretaceous hydrothermal breccia complex in the Coastal Cordillera of northern Chile. The current resource, which includes the neighboring Alice Cu-Mo porphyry deposit, is estimated at 236.6 Mt grading 0.48% Cu, 0.10 g/t Au, and 135 ppm Mo. Local wall rocks consist of a thick sequence of broadly coeval rhyolite to rhyodacite lapilli tuffs (128.7 ± 1.3 Ma; U-Pbzircon) and two major intrusions: the Cachiyuyito tonalite and Ruta Cinco granodiorite batholith (92.0 ± 1.0 Ma; U-Pbzircon). Previous studies at Productora concluded the deposit had strong affinities with the iron oxide copper-gold (IOCG) clan and likened the deposit to Candelaria. Based on new information, we document the deposit geology in detail and propose a new genetic model and alternative classification as a magmatic-hydrothermal breccia complex with closer affinities to porphyry systems. Hydrothermal and tectonic breccias, veins, and alteration assemblages at Productora define five paragenetic stages: stage 1 quartz-pyrite–cemented breccias associated with muscovite alteration, stage 2 chaotic matrix-supported tectonic-hydrothermal breccia with kaolinite-muscovite-pyrite alteration, stage 3 tourmaline-pyrite-chalcopyrite ± magnetite ± biotite-cemented breccias and associated K-feldspar ± albite alteration, stage 4 chalcopyrite ± pyrite ± muscovite, illite, epidote, and chlorite veins, and stage 5 calcite veins. The Productora hydrothermal system crosscuts earlier-formed sodic-calcic alteration and magnetite-apatite mineralization associated with the Cachiyuyito stock. Main-stage mineralization at Productora was associated with formation of the stage 3 hydrothermal breccia. Chalcopyrite is the dominant hypogene Cu mineral and occurs predominantly as breccia cement and synbreccia veins with pyrite. The Alice Cu-Mo porphyry deposit is characterized by disseminated chalcopyrite and quartz-pyrite-chalcopyrite ± molybdenite vein stockworks hosted by a granodiorite porphyry stock. Alice is spatially associated with the Silica Ridge lithocap, which is characterized by massive, fine-grained, quartz-altered rock above domains of alunite, pyrophyllite, and dickite. Rhenium-Os dating of molybdenite indicates that main-stage mineralization at Productora occurred at 130.1 ± 0.6 Ma, and at 124.1 ± 0.6 Ma in the Alice porphyry. Chalcopyrite and pyrite from Productora have δ34Ssulfide values from –8.5 to +2.2‰, consistent with a magmatic sulfur source and fluids evolving under oxidizing conditions. No significant input from evaporite- or seawater-sourced fluids was detected. Stage 3 tourmalines have average initial Sr of 0.70397, consistent with an igneous-derived Sr source. The Productora magmatic-hydrothermal breccia complex formed as a result of explosive volatile fluid release from a hydrous intrusive complex. Metal-bearing fluids were of magmatic affinity and evolved under oxidizing conditions. Despite sharing many similarities with the Andean IOCG clan (strong structural control, regional sodic-calcic alteration, locally anomalous U), fluid evolution at the Productora Cu-Au-Mo deposit is more consistent with that of a porphyry-related magmatic hydrothermal breccia (sulfur-rich, acid alteration assemblages and relatively low magnetite contents, &lt;5 vol %). The Productora camp is an excellent example of the close spatial association of Mesozoic magnetite-apatite, porphyry, and magmatic-hydrothermal breccia mineralization styles, a relationship seen throughout the Coastal Cordillera of northern Chile.
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15

Schlegel, Tobias U., Renee Birchall, Tina D. Shelton, and James R. Austin. "MAPPING THE MINERAL ZONATION AT THE ERNEST HENRY IRON OXIDE COPPER-GOLD DEPOSIT: VECTORING TO Cu-Au MINERALIZATION USING MODAL MINERALOGY." Economic Geology 117, no. 2 (March 1, 2022): 485–94. http://dx.doi.org/10.5382/econgeo.4915.

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Abstract Iron oxide copper-gold (IOCG) deposits form in spatial and genetic relation to hydrothermal iron oxide-alkali-calcic-hydrolytic alteration and thus show a mappable zonation of mineral assemblages toward the orebody. The mineral zonation of a breccia matrix-hosted orebody is efficiently mapped by regularly spaced samples analyzed by the scanning electron microscopy-integrated mineral analyzer technique. The method results in quantitative estimates of the mineralogy and allows the reliable recognition of characteristic alteration as well as mineralization-related mineral assemblages from detailed mineral maps. The Ernest Henry deposit is located in the Cloncurry district of Queensland and is one of Australia’s significant IOCG deposits. It is known for its association of K-feldspar altered clasts with iron oxides and chalcopyrite in the breccia matrix. Our mineral mapping approach shows that the hydrothermal alteration resulted in a characteristic zonation of minerals radiating outward from the pipe-shaped orebody. The mineral zonation is the result of a sequence of sodic alteration followed by potassic alteration, brecciation, and, finally, by hydrolytic (acid) alteration. The hydrolytic alteration primarily affected the breccia matrix and was related to economic mineralization. Alteration halos of individual minerals such as pyrite and apatite extend dozens to hundreds of meters beyond the limits of the orebody into the host rocks. Likewise, the Fe-Mg ratio in hydrothermal chlorites changes systematically with respect to their distance from the orebody. Geochemical data obtained from portable X-ray fluorescence (p-XRF) and petrophysical data acquired from a magnetic susceptibility meter and a gamma-ray spectrometer support the mineralogical data and help to accurately identify mineral halos in rocks surrounding the ore zone. Specifically, the combination of mineralogical data with multielement data such as P, Mn, As, P, and U obtained from p-XRF and positive U anomalies from radiometric measurements has potential to direct an exploration program toward higher Cu-Au grades.
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16

Courtney-Davies, Liam, Cristiana L. Ciobanu, Simon R. Tapster, Nigel J. Cook, Kathy Ehrig, James L. Crowley, Max R. Verdugo-Ihl, Benjamin P. Wade, and Daniel J. Condon. "OPENING THE MAGMATIC-HYDROTHERMAL WINDOW: HIGH-PRECISION U-Pb GEOCHRONOLOGY OF THE MESOPROTEROZOIC OLYMPIC DAM Cu-U-Au-Ag DEPOSIT, SOUTH AUSTRALIA." Economic Geology 115, no. 8 (August 27, 2020): 1855–70. http://dx.doi.org/10.5382/econgeo.4772.

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Abstract Establishing timescales for iron oxide copper-gold (IOCG) deposit formation and the temporal relationships between ores and the magmatic rocks from which hydrothermal, metal-rich fluids are sourced is often dependent on low-precision data, particularly for deposits that formed during the Proterozoic. Unlike accessory minerals routinely used to track hydrothermal mineralization, iron oxides are dominant components of IOCG systems and are therefore pivotal to understanding deposit evolution. The presence of ubiquitous, magmatic-hydrothermal U-(Pb)-W-Sn-Mo–bearing zoned hematite resolves a range of geochronological issues concerning formation of the ~1.6 Ga Olympic Dam IOCG deposit, South Australia, at up to ~0.05% precision (207Pb/206Pb weighted mean; 2σ) using isotope dilution-thermal ionization mass spectrometry (ID-TIMS). Coupled with chemical abrasion-ID-TIMS zircon dates from host granite and volcanic rocks within and enclosing the ore-body, a confident magmatic-hydrothermal chronology is defined. The youngest zircon date from the granite intrusion hosting Olympic Dam indicates magmatism was occurring up until 1593.28 ± 0.26 Ma. The orebody was principally formed during a major mineralizing event following granite uplift and during cupola collapse, whereby the hematite with the oldest age is recorded in the outer shell of the deposit at 1591.27 ± 0.89 Ma, ~2 m.y. later than the youngest documented magmatic zircon. Hematite dates captured throughout major lithologies, different ore zones, and the ~2-km vertical extent of the deposit support ~2 m.y. of hydrothermal activity. New age constraints on the spatial-temporal evolution of the formation of Olympic Dam are considered with respect to a mantle to crustal continuum model. Cyclical tapping of magma reservoirs to maintain crystal mushes for extended time periods and incremental building of batholiths on the million-year scale prior to main mineralization pulses can explain the ~2-m.y. temporal window temporal window inferred from the data. Despite the challenge of reconciling such an extended window with contemporary models for porphyry deposits (≤1 m.y.), formation of Proterozoic ore deposits has been addressed at high-precision and supports the case that giant IOCG deposits may form over millions of years.
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17

Huang, Xiao-Wen, Anne-Aurélie Sappin, Émilie Boutroy, Georges Beaudoin, and Sheida Makvandi. "Trace Element Composition of Igneous and Hydrothermal Magnetite from Porphyry Deposits: Relationship to Deposit Subtypes and Magmatic Affinity." Economic Geology 114, no. 5 (August 1, 2019): 917–52. http://dx.doi.org/10.5382/econgeo.4648.

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Abstract The trace element composition of igneous and hydrothermal magnetite from 19 well-studied porphyry Cu ± Au ± Mo, Mo, and W-Mo deposits was measured by laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) and then classified by partial least squares-discriminant analysis (PLS-DA) to constrain the factors explaining the relationships between the chemical composition of magnetite and the magmatic affinity and porphyry deposit subtypes. Igneous magnetite can be discriminated by relatively high P, Ti, V, Mn, Zr, Nb, Hf, and Ta contents but low Mg, Si, Co, Ni, Ge, Sb, W, and Pb contents, in contrast to hydrothermal magnetite. Compositional differences between igneous and hydrothermal magnetite are mainly controlled by the temperature, oxygen fugacity, cocrystallized sulfides, and element solubility/mobility that significantly affect the partition coefficients between magnetite and melt/fluids. Binary diagrams based on Ti, V, and Cr contents are not enough to discriminate igneous and hydrothermal magnetite in porphyry deposits. Relatively high Si and Al contents discriminate porphyry W-Mo hydrothermal magnetite, probably reflecting the control by high-Si, highly differentiated, granitic intrusions for this deposit type. Relatively high Mg, Mn, Zr, Nb, Sn, and Hf but low Ti and V contents discriminate porphyry Au-Cu hydrothermal magnetite, most likely resulting from a combination of mafic to intermediate intrusion composition, high chlorine in fluids, relatively high oxygen fugacity, and low-temperature conditions. Igneous or hydrothermal magnetite from Cu-Mo, Cu-Au, and Cu-Mo-Au deposits cannot be discriminated from each other, probably due to similar intermediate to felsic intrusion composition, melt/fluid composition, and conditions such as temperature and oxygen fugacity for the formation of these deposits. The magmatic affinity of porphyritic intrusions exerts some control on the chemical composition of igneous and hydrothermal magnetite in porphyry systems. Igneous and hydrothermal magnetite related to alkaline magma is relatively rich in Mg, Mn, Co, Mo, Sn, and high field strength elements (HFSEs), perhaps due to high concentrations of chlorine and fluorine in magma and exsolved fluids, whereas those related to calc-alkaline magma are relatively rich in Ca but depleted in HFSEs, consistent with the high Ca but low HFSE magma composition. Igneous and hydrothermal magnetite related to high-K calc-alkaline magma is relatively rich in Al, Ti, Sc, and Ta, due to a higher temperature of formation or enrichment of these elements in melt/fluids. Partial least squares-discriminant analysis on hydrothermal magnetite compositions from porphyry Cu, iron oxide copper-gold (IOCG), Kiruna-type iron oxide-apatite (IOA), and skarn deposits around the world identify important discriminant elements for these deposit types. Magnetite from porphyry Cu deposits is characterized by relatively high Ti, V, Zn, and Al contents, whereas that from IOCG deposits can be discriminated from other types of magnetite by its relatively high V, Ni, Ti, and Al contents. IOA magnetite is discriminated by higher V, Ti, and Mg but lower Al contents, whereas skarn magnetite can be separated from magnetite from other deposit types by higher Mn, Mg, Ca, and Zn contents. Decreased Ti and V contents in hydrothermal magnetite from porphyry Cu and IOA, to IOCG, and to skarn deposits may be related to decreasing temperature and increasing oxygen fugacity. The relative depletion of Al in IOA magnetite is due to its low magnetite-silicate melt partition coefficient, immobility of Al in fluids, and earlier, higher-temperature magmatic or magmatic-hydrothermal formation of IOA deposits. The relative enrichment of Ni in IOCG magnetite reflects more mafic magmatic composition and less competition with sulfide, whereas elevated Mn, Mg, Ca, and Zn in skarn magnetite results from enrichment of these elements in fluids via more intensive fluid-carbonate rock interaction.
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18

Skirrow, Roger G., James Murr, Anthony Schofield, David L. Huston, Simon van der Wielen, Karol Czarnota, Rohan Coghlan, et al. "Mapping iron oxide Cu-Au (IOCG) mineral potential in Australia using a knowledge-driven mineral systems-based approach." Ore Geology Reviews 113 (October 2019): 103011. http://dx.doi.org/10.1016/j.oregeorev.2019.103011.

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19

Kontonikas-Charos, Alkis, Cristiana L. Ciobanu, Nigel J. Cook, Kathy Ehrig, Roniza Ismail, Sasha Krneta, and Animesh Basak. "Feldspar mineralogy and rare-earth element (re)mobilization in iron-oxide copper gold systems from South Australia: a nanoscale study." Mineralogical Magazine 82, S1 (February 28, 2018): S173—S197. http://dx.doi.org/10.1180/minmag.2017.081.040.

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ABSTRACTNanoscale characterization (TEM on FIB-SEM-prepared foils) was undertaken on feldspars undergoing transformation from early post-magmatic (deuteric) to hydrothermal stages in granites hosting the Olympic Dam Cu-U-Au-Ag deposit, and from the Cu-Au skarn at Hillside within the same iron-oxide copper-gold (IOCG) province, South Australia. These include complex perthitic textures, anomalously Ba-, Fe-, or REE-rich compositions, and REE-flourocarbonate + molybdenite assemblages which pseudomorph pre-existing feldspars. Epitaxial orientations between cryptoperthite (magmatic), patch perthite (dueteric) and replacive albite (hydrothermal) within vein perthite support interface-mediated reactions between pre-existing alkali-feldspars and pervading fluid, irrespective of micro-scale crystal morphology. Such observations are consistent with a coupled dissolution-reprecipitation reaction mechanism, which assists in grain-scale element remobilization via the generation of transient interconnected microporosity. Micro-scale aggregates of hydrothermal hyalophane (Ba-rich K-feldspar), crystallizing within previously albitized areas of andesine, reveal a complex assemblage of calc-silicate, As-bearing fluorapatite and Fe oxides along reaction boundaries in the enclosing albite-sericite assemblage typical of deuteric alteration. Such inclusions are good REE repositories and their presence supports REE remobilization at the grain-scale during early hydrothermal alteration. Iron-metasomatism is recognized by nanoscale maghemite inclusions within ‘red-stained’ orthoclase, as well as by hematite in REE-fluorocarbonates, which reflect broader-scale zonation patterns typical for IOCG systems. Potassium-feldspar from the contact between alkali-granite and skarn at Hillside is characterized by 100–1000 ppm REE, attributable to pervasive nanoscale inclusions of calc-silicates, concentrated along microfractures, or pore-attached. Feldspar replacement by REE-fluorcarbonates at Olympic Dam and nanoscale calc-silicate inclusions in feldspar at Hillside are both strong evidence for the role of feldspars in concentrating REE during intense metasomatism. Differences in mineralogical expression are due to the availability of associated elements. Lattice-scale intergrowths of assemblages indicative of Fe-metasomatism, REE-enrichment and sulfide deposition at Olympic Dam are evidence for a spatial and temporal relationship between these processes.
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20

Bauer, Tobias E., Edward P. Lynch, Zmar Sarlus, David Drejing-Carroll, Olof Martinsson, Nicolai Metzger, and Christina Wanhainen. "Structural Controls on Iron Oxide Copper-Gold Mineralization and Related Alteration in a Paleoproterozoic Supracrustal Belt: Insights from the Nautanen Deformation Zone and Surroundings, Northern Sweden." Economic Geology 117, no. 2 (March 1, 2022): 327–59. http://dx.doi.org/10.5382/econgeo.4862.

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Abstract The Nautanen deformation zone in the Gällivare area of northern Sweden is a highly Cu-mineralized, magnetite-rich, large-scale shear zone with a long-lived (~100 m.y.) deformation, hydrothermal alteration, and mineralization history. This composite structure hosts the Aitik porphyry Cu-Au-Ag ± Mo deposit and several Cu-Au ± Fe ± Ag ± Mo occurrences assigned to the iron oxide copper-gold (IOCG) deposit class. The Nautanen deformation zone was a locus for polyphase deformation and intermittent metasomatic-hydrothermal activity that overprinted middle Orosirian (ca. 1.90–1.88 Ga) continental arc-related volcanic-plutonic rocks. The deformation zone is characterized by intense shearing fabrics that form a series of subvertical to moderately W-dipping, NNW-SSE–trending, first-order shear zones with oblique reverse kinematics and related NNE-SSW–oriented second-order shear zones that control hydrothermal alteration patterns and Cu-Au mineralization. Hydrothermal alteration in the study area formed during several phases. Volcanic-volcaniclastic rocks to the east and west of the Nautanen deformation zone display low to moderately intense, pervasive to selectively pervasive (i.e., patchy zones or bands, disseminations) sericite ± feldspar, amphibole + biotite + magnetite ± tourmaline, and K-feldspar + hematite alteration. Both the amphibole + biotite and K-feldspar + hematite associations occur adjacent to NNW- and NE-oriented deformation zones and are locally associated with minor sulfide. Within the deformation zone, a moderate to intense biotite + amphibole + garnet + magnetite + tourmaline + sericite alteration assemblage is typically associated with chalcopyrite + pyrrhotite + pyrite and forms linear and subparallel, mainly NNW-oriented seams, bands, and zones that locally appear to overprint possibly earlier scapolite + sericite ± feldspar alteration. Late-stage epidote ± quartz ± feldspar alteration (retrograde saussuritization) forms selectively pervasive zones and epidote veinlets across the area and is partly related to brittle faulting. A magnetite-amphibole-biotite–rich, penetrative S1 foliation records shortening during early Svecokarelian-related deformation (D1) and can be related to ca. 1.88 to 1.87 Ga arc accretion processes and basin inversion that overlaps with regional peak metamorphism to near mid-amphibolite facies conditions and a potential initial Cu mineralization event. Folding and repeated shearing along the Nautanen deformation zone can be assigned to a second, late-Svecokarelian deformation event (D2 stage, ca. 1.82–1.79 Ga) taking place at a higher crustal level. This D2 deformation phase is related to late-stage accretionary processes active during a transition to a stage of postorogenic collapse, and it was accompanied by abundant, syntectonic intrusions. D2-related magmatism produced high-temperature and low-pressure conditions and represents a regional magmatic-hydrothermal event that controlled the recrystallization/remobilization of magnetite, biotite, and amphibole. Associated shear zone reactivation during D2 favors the utilization of the Nautanen deformation zone as a fluid conduit, which preferentially controlled the siting and formation of epigenetic Cu-Au mineralization with distinctive IOCG characteristics within second-order shear zones.
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21

Kostin, Aleksey. "Mineralization in the andesitic lava from Kildyam volcanic complex, central Yakutia, Russia." IOP Conference Series: Earth and Environmental Science 906, no. 1 (November 1, 2021): 012006. http://dx.doi.org/10.1088/1755-1315/906/1/012006.

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Abstract This contribution presents the first detailed analysis of a new volcanic succession of olivine-pyroxenites, andesite, and dacite discovered in the Kildyam Late Jurassic complex in Central Yakutia. Petrographic and microprobe studies confirmed the liquid immiscibility in silicate melts during crystallization. Immiscible liquids are preserved as globules of one glass in another in andesites and as melted inclusions of native iron in matrix, clinopyroxene and plagioclase phenocrysts. Our analyses reveal the complex textural relationships between silicates and Fe-oxides, native iron and (Cu, Pb, Ag and Au)-rich phases, and provide unequivocal textural evidences, not observed previously. Purpose of this research is to preserve a very important data on IO (Iron Oxide) or IOCG (Iron Oxide Copper Gold) mineralization. Obtained results support occurrence and diverse of gold, silver, copper and lead minerals in magnetite lavas. During the early stage of fine-grained subvolcanic olivine-clinopyroxenite end pyrrhotite, globular igneous sulfides is a first proposed style of economic deposit formation. The second proposed style of economic mineralization in Kildyam is to be a magnetite-bearing lava; iron enrichment of the melilitic melt phase, followed by iron depletion and silica enrichment. The vesicle-hosted alloys and sulfides provide significant new data on metal transport and precipitation from high-temperature magmatic vapors. During syneruptive vapor phase exsolution, volatile metals (Cu-Zn, Fe-Al-Cu, Ni-Fe-Cu-Sn) and Ag-Cu-sulfides contribute to the formation of economic concentrations. Major conclusions contribute to 3-step genetic model. (1) Early-formed magmatic minerals led to partial dissolution of olivine-clinopyroxenite and their enrichment in Cu, Co and Ni relative to other metals, while troilite globules droplets grew.(2) First stage of division into two immiscible silicate and sulfide melt liquids (a) K-rich dacitic and rhyolithic glass, and (b) vesicles of heavy sulfide minerals with a large segregations and drops of native iron. (3) Lava of fused magnetite crystals and voids enriched in silver and gold, and (b) globular disseminated chalcopyrite in mineralized melilitic rocks.
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22

Courtney-Davies, Ciobanu, Verdugo-Ihl, Slattery, Cook, Dmitrijeva, Keyser, et al. "Zircon at the Nanoscale Records Metasomatic Processes Leading to Large Magmatic–Hydrothermal Ore Systems." Minerals 9, no. 6 (June 16, 2019): 364. http://dx.doi.org/10.3390/min9060364.

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The petrography and geochemistry of zircon offers an exciting opportunity to better understand the genesis of, as well as identify pathfinders for, large magmatic–hydrothermal ore systems. Electron probe microanalysis, laser ablation inductively coupled plasma mass spectrometry, high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) imaging, and energy-dispersive X-ray spectrometry STEM mapping/spot analysis were combined to characterize Proterozoic granitic zircon in the eastern Gawler Craton, South Australia. Granites from the ~1.85 Ga Donington Suite and ~1.6 Ga Hiltaba Suite were selected from locations that are either mineralized or not, with the same style of iron-oxide copper gold (IOCG) mineralization. Although Donington Suite granites are host to mineralization in several prospects, only Hiltaba Suite granites are considered “fertile” in that their emplacement at ~1.6 Ga is associated with generation of one of the best metal-endowed IOCG provinces on Earth. Crystal oscillatory zoning with respect to non-formula elements, notably Fe and Cl, are textural and chemical features preserved in zircon, with no evidence for U or Pb accumulation relating to amorphization effects. Bands with Fe and Ca show mottling with respect to chloro–hydroxy–zircon nanoprecipitates. Lattice defects occur along fractures crosscutting such nanoprecipitates indicating fluid infiltration post-mottling. Lattice stretching and screw dislocations leading to expansion of the zircon structure are the only nanoscale structures attributable to self-induced irradiation damage. These features increase in abundance in zircons from granites hosting IOCG mineralization, including from the world-class Olympic Dam Cu–U–Au–Ag deposit. The nano- to micron-scale features documented reflect interaction between magmatic zircon and corrosive Fe–Cl-bearing fluids in an initial metasomatic event that follows magmatic crystallization and immediately precedes deposition of IOCG mineralization. Quantification of α-decay damage that could relate zircon alteration to the first percolation point in zircon gives ~100 Ma, a time interval that cannot be reconciled with the 2–4 Ma period between magmatic crystallization and onset of hydrothermal fluid flow. Crystal oscillatory zoning and nanoprecipitate mottling in zircon intensify with proximity to mineralization and represent a potential pathfinder to locate fertile granites associated with Cu–Au mineralization.
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23

Hunt, Julie A., Tim Baker, James Cleverley, Garry J. Davidson, Anthony E. Fallick, and Derek J. Thorkelson. "Fluid inclusion and stable isotope constraints on the origin of Wernecke Breccia and associated iron oxide – copper – gold mineralization, Yukon." Canadian Journal of Earth Sciences 48, no. 10 (October 2011): 1425–45. http://dx.doi.org/10.1139/e11-044.

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Iron oxide – Cu ± Au ± U ± Co (IOCG) mineralization is associated with numerous Proterozoic breccia bodies, collectively known as Wernecke Breccia, in Yukon Territory, Canada. Multiphase breccia zones occur in areas underlain by Paleoproterozoic Wernecke Supergroup metasedimentary rocks and are associated with widespread sodic, potassic, and carbonate alteration assemblages. Fluid inclusion data indicate syn-breccia fluids were hot (185–350 °C) saline (24–42 wt.% NaCl equivalent) NaCl–CaCl2–H2O brines. Estimates of fluid pressure vary from 0.4 to 2.4 kbar (1 kbar = 100 MPa). Carbon and oxygen isotopic compositions of breccia-related carbonates range from ~–11‰ to +1.5‰ (Pee Dee belemnite (PDB)) and –2‰ to 20‰ (Vienna standard mean ocean water (V-SMOW); δ18Owater ~–8‰ to +15‰), respectively. δ13C and δ18O values for host Wernecke Supergroup limestone/dolostone vary from ~–2‰ to 1.6‰ and 12‰ to 25‰, respectively. Sulfur isotopic compositions of hydrothermal sulfides and sulfate vary from ~–12‰ to +13‰ and +8‰ to +17‰ (Cañon Diablo Troilite (CDT)), respectively. Syn-breccia biotite, muscovite, and actinolite have δD and δ18O values of ~–141‰ to –18‰ and +7‰ to +12‰ (V-SMOW; δ18Owater ~7‰ to 11‰), respectively. The Wernecke Breccias and the associated IOCG mineralization appear to have formed from largely nonmagmatic fluids — based on isotopic, fluid inclusion, and geological data. The emerging hypothesis is that periodic overpressuring of dominantly formational/metamorphic water led to repeated brecciation and mineral precipitation. The weight of overlying sedimentary rocks led to elevated fluid temperatures and pressures; fluid flow may have been driven by tectonics and (or) gravity with metals scavenged from host strata.
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24

Groves, David I., Liang Zhang, and M. Santosh. "Subduction, mantle metasomatism, and gold: A dynamic and genetic conjunction." GSA Bulletin 132, no. 7-8 (November 4, 2019): 1419–26. http://dx.doi.org/10.1130/b35379.1.

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Abstract Global gold deposit classes are enigmatic in relation to first-order tectonic scale, leading to controversial genetic models and exploration strategies. Traditionally, hydrothermal gold deposits that formed through transport and deposition from auriferous ore fluids are grouped into specific deposit types such as porphyry, skarn, high- and low-sulfidation–type epithermal, gold-rich volcanogenic massive sulfide (VMS), Carlin-type, orogenic, and iron-oxide copper-gold (IOCG), and intrusion-related gold deposits (IRGDs). District-scale mineral system approaches propose interrelated groups such as porphyry Cu-Au, skarn Cu-Au-Ag, and high-sulfidation Au-Ag. In this study, the temporal evolution of subduction-related processes in convergent margins was evaluated to propose a continuum of genetic models that unify the various types of gold deposits. At the tectonic scale of mineral systems, all hydrothermal gold deposits are interrelated in that they formed progressively during the evolution of direct or indirect subduction-related processes along convergent margins. Porphyry-related systems formed initially from magmatic-hydrothermal fluids related to melting of fertile mantle to initiate calc-alkaline to high-K felsic magmatism in volcanic arcs directly related to subduction. Formation of gold-rich VMS systems was related to hydrothermal circulation driven by magmatic activity during rifting of oceanic arcs. Orogenic gold deposits formed largely through fluids derived from devolatilization of the downgoing slab and overlying sediment wedge during late transpression in the orogenic cycle. Carlin-type deposits, IRGDs, and some continental-arc porphyry systems formed during the early stages of orogenic collapse via fluids directly or indirectly related to hybrid magmatism from melting of lithosphere that was metasomatized and gold-fertilized by earlier fluid release from subduction zones near margins of continental blocks. The IOCGs were formed during postorogenic asthenosphere upwelling beneath such subduction-related metasomatized and fertilized lithospheric blocks via fluid release and explosive emplacement of volatile-rich melts. Thus, importantly, subduction is clearly recognized as the key unifying dynamic factor in gold metallogenesis, with subduction-related fluids or melts providing the critical ore components for a wide variety of gold-rich deposit types.
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25

Gauthier, Michel, and Francis Chartrand. "Metallogeny of the Grenville Province revisited." Canadian Journal of Earth Sciences 42, no. 10 (October 1, 2005): 1719–34. http://dx.doi.org/10.1139/e05-051.

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Four new petrogenetic and metallogenic models are proposed herein to explain the formation of important mineral deposits in the Grenville Province, providing a framework from which to reappraise Grenvillian mineral potential. Recognition of a high-pressure metamorphic belt within the Grenville Province suggests a potential for eclogite-hosted rutile deposits, an important and much-sought commodity. A recently developed Norwegian model proposes that anorthosite genesis occurred through lower crust underplating and coeval partial melting, rather than by plume magmatism. Applied to the Grenville Province, the new petrogenetic model may provide insight into the widespread occurrence of platinum group element (PGE) poor nickel showings and the distribution of chromite, Ti-rich, and low-Ti iron-oxide deposits within the Grenville and adjacent terranes. A new type of sedimentary–exhalative (SEDEX) mineralization formed by oxidized brines has been defined following the discovery of new deposits in Australia. Applied to the Grenville Province, it provides a possible explanation for two long-recognized features of marble-hosted zinc deposits: (i) the presence of meta-siderite beds occurring as distal haloes around SEDEX zinc deposits, and (ii) the mutually exclusive division of these SEDEX deposits into massive sulphide and nonsulphide groups. The discovery of the giant Olympic Dam iron-oxide copper–gold (IOCG) deposit in Australia renewed the interest in magmatic low-Ti iron-oxide deposits in the Grenville Province that have been known and mined since early colonial times. Subsequent exploration in the northeastern part of the Grenville Province revealed the presence of breccia-hosted Cu–Au–U – rare-earth element (REE)-bearing iron-oxide mineralization. This deposit and other low-Ti iron-oxide deposits in the southwestern Grenville Province have a previously undocumented close spatial and temporal association with Ti-rich iron-oxide deposits. These examples demonstrate how new petrogenetic, tectonic, and ore deposit models developed in unmetamorphosed rocks can be successfully adapted to high-grade terranes, where they stimulate mineral exploration in these challenging conditions. Furthermore, by tracking the formation of ore deposits in the lower crust, the existence of unsuspected metallogenic associations in the higher crust, such as the low-Ti and high-Ti iron-oxide association observed in the Grenville Province, may be revealed.
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26

Campos, Daniela Schievano de, Adalene Moreira Silva, Catarina Laboure Bemfica Toledo, Marcelo Juliano de Carvalho, Vinícius Gomes Rodrigues, and Kawinã Araujo. "Prospectivity analysis of gold and iron oxide copper-gold-(silver) mineralizations from the Faina Greenstone Belt, Brazil, using multiple data sets." Brazilian Journal of Geology 47, no. 4 (December 2017): 561–90. http://dx.doi.org/10.1590/2317-4889201720170012.

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ABSTRACT: The Faina Greenstone Belt is located in the southern sector of the Goiás Archean Block and has been investigated since the 18th century because of its gold deposits. Recent studies have revealed the polymetallic potential of the belt, which is indicated by anomalous levels of Ag, Cu, Fe and Co in addition to Mn, Ba, Li, Ni, Cr and Zn. This study was developed based on a detailed analysis of two selected target sites, Cascavel and Tinteiro, and multiple data sets, such as airborne geophysics, geochemistry and geological information. These datasets were used to create a final prospectivity map using the fuzzy logic technique. The gold mineralization of Cascavel target is inserted in an orogenic system and occurs in two overlapping quartz veins systems, called Mestre-Cascavel and Cuca, embedded in quartzite with an average thickness 50 cm and guidance N45º-60ºW/25ºSW with free coarse gold in grains 2-3 mm to 3 cm. The prospectivity map created for this prospect generated four first-order favorable areas for mineralization and new medium-favorability foci. The Tinteiro area, derived from studies conducted by Orinoco do Brasil Mineração Ltda., shows polymetallic mineralization associated with an iron oxide-copper-gold ore deposit (IOCG) system posterior to Cascavel target mineralization. Its prospectivity map generated 19 new target sites with the potential for Au, Cu and Ag mineralization, suggesting new directions for future prospecting programs.
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27

del Real, I., J. F. H. Thompson, A. C. Simon, and M. Reich. "Geochemical and Isotopic Signature of Pyrite as a Proxy for Fluid Source and Evolution in the Candelaria-Punta del Cobre Iron Oxide Copper-Gold District, Chile." Economic Geology 115, no. 7 (November 1, 2020): 1493–518. http://dx.doi.org/10.5382/econgeo.4765.

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Abstract Pyrite is ubiquitous in the world-class iron oxide copper-gold (IOCG) deposits of the Candelaria-Punta del Cobre district, documented from early to late stages of mineralization and observed in deep and shallow levels of mineralized bodies. Despite its abundance, the chemical and isotopic signature of pyrite from the Candelaria-Punta del Cobre district, and most IOCG deposits worldwide, remains poorly understood. We evaluated in situ chemical and isotopic variations at the grain scale in a set of pyrite-bearing samples collected throughout the district in order to characterize and further understand the nature of mineralization in this IOCG system. Our multianalytical approach integrated synchrotron micro-X-ray fluorescence (μ-XRF) mapping of pyrite grains with electron probe microanalysis and laser ablation-inductively coupled plasma-mass spectrometry data, and sulfur isotope determinations using secondary ion mass spectrometry (SIMS) complemented with bulk sulfur isotope analyses of coeval pyrite, chalcopyrite, and anhydrite. Synchrotron μ-XRF elemental concentration maps of individual pyrite grains reveal a strong zonation of Co, Ni, As, and Se. The observed relationships between Ni and Se are interpreted to reflect changes in temperature and redox conditions during ore formation and provide constraints on fluid evolution. Co and Ni concentrations and ratios suggest contributions from magmas of mafic-intermediate composition. Pyrite chemical concentrations reflect potential stratigraphic controls, where the sample from the upper part of the stratigraphy diverges from trends formed by the rest of the sample set from lower stratigraphic levels. The SIMS δ34S values of pyrite (and chalcopyrite) range between –2 up to 10‰, and bulk δ34S values of pyrite range between 4 up to 12‰. The majority of the δ34S analyses, falling between –1 and 2‰, indicate a magmatic source for sulfur and, by inference, for the hydrothermal ore fluid(s). Variation in the δ34S signature can be explained by changes in the redox conditions, fluid sources, and/or the temperature of the hydrothermal fluid. The Se/S ratio combined with δ34S values in pyrite is consistent with mixing between a magmatic-hydrothermal fluid and a fluid with a probable basinal signature. The results of this study are consistent with the hydrothermal fluids responsible for mineralization in the Candelaria-Punta del Cobre district being predominantly of magmatic origin, plausibly from mafic-intermediate magmas based on the Ni-Co content in pyrite. External fluid incursion, potentially from a basinal sedimentary source, occurred late in the evolution of the system, adding additional reduced sulfur as pyrite. There is no evidence to suggest that the late fluid added significant Cu-Au mineralization, but this cannot be ruled out. Finally, the data reveal that trace element ratios coupled with spatially resolved sulfur isotope data in pyrite are powerful proxies to track the magmatic-hydrothermal evolution of IOCG systems and help constrain the source of their contained metals.
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28

Wang, Tianguo, Chunkit Lai, and Huan Li. "Geology and Genesis of Xianglushan Fe-Cu Orefield in Sichuan (SW China): Evidence from C-O-S-Pb Isotopes." Minerals 9, no. 6 (June 1, 2019): 338. http://dx.doi.org/10.3390/min9060338.

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The Proterozoic Xianglushan Fe-Cu orefield (western Sichuan) is located in the Huili–Dongchuan ore belt on the southwestern margin of the Yangtze Block in SW China. The orefield has experienced complex magmatotectonic activities, and hosts a wide variety of Fe oxide-(Cu-Au) deposits. At Xianglushan, the orebodies are made of stratabound magnetite–hematite orebodies superimposed by vein-type chalcopyrite mineralization. The stratabound Fe orebodies are hosted mainly in the Proterozoic volcanic-sedimentary rocks of the lower Yinmin Formation, whilst the Cu vein or stockwork ores were mainly emplaced into the upper part of the footwall volcanic rocks and the lower part of the Fe orebodies. We divided the alteration/mineralization and their fluid inclusions (FIs) into the (I) sodic-calcic alteration, (II) potassic-silicic-sericite alteration and Fe-(Cu) mineralization, and (III) carbonate alteration and Cu mineralization stages. Stage II FIs are mainly two-phase (vapor-liquid), and are featured by medium temperature (348 to 379 °C) and high salinity (21.8 to 22.9 wt % NaCl eqv). Their generally negative calcite δ13C (−4.1‰ to −3.1‰) and δ18OH2O (12.2‰ to 15.3‰) values reveal that the Stage II ore fluids have had a seawater-magmatic fluid mixed source. Late Stage II pyrite has δ34S (−3.3‰ to 13.7‰), 206Pb/204Pb (17.663 to 18.982), 207Pb/204Pb (15.498 to 15.824) and 208Pb/204Pb (37.784 to 38.985), suggesting that the ore-forming materials were derived from dominantly upper crustal source. Stage III FIs are also mainly two-phase (vapor-liquid), and are featured by lower temperature (206 to 267 °C) and salinity (19.0 to 22.5 wt % NaCl eqv) than their Stage II counterparts. The Stage III ore fluids were also likely derived from a meteoric–magmatic mixed source with greater magmatic influence, as indicated by the generally negative calcite δ13C (−6.9‰ to −4.6‰) and δ18OH2O (6.3‰ to 9.2‰) values. Similar to the late Stage II pyrite, the Stage III chalcopyrite δ34S (−4.6‰ to 5.2‰) and Pb isotopes (206Pb/204Pb = 18.198 to 18.987; 207Pb/204Pb = 15.534 to 15.876; and 208Pb/204Pb = 37.685 to 39.476) also suggest a crustal ore-forming material source. Therefore, we suggest that the Fe-(Cu) and Cu mineralization at Xianglushan had similar ore fluid and material sources, although the magmatic influence increased in the later stage. This resembles many Fe-(Cu) deposits in the Huili–Dongchuan ore belt. We conclude that the Xianglushan Fe-Cu deposits are both similar to and different from typical iron-oxide copper gold (IOCG) deposits in terms of alteration styles and hydrothermal mineral assemblages, and are thus best classified as IOCG-like deposits hosted in submarine volcanic-sedimentary rocks. Considering the Mesoproterozoic regional tectonics in the southwestern Yangtze Block, we propose that the Xianglushan ore formation occurred in an intra-/back-arc inversion setting, possibly related to the closure of the Anning ocean basin.
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29

Clark, T., A. Gobeil, and J. David. "Iron oxide - copper - gold-type and related deposits in the Manitou Lake area, eastern Grenville Province, Quebec: variations in setting, composition, and style." Canadian Journal of Earth Sciences 42, no. 10 (October 1, 2005): 1829–47. http://dx.doi.org/10.1139/e05-048.

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The Manitou Lake area (Kwyjibo and Lac Marmont sectors), located in Quebec's eastern Grenville Province, contains magnetite-rich deposits with variable morphological, mineralogical, and chemical characteristics. Most Kwyjibo sector deposits are rich in Cu, rare-earth elements (REE), Y, P, F, and Ag and are anomalous in Th, U, Mo, W, Zr, and Au, and Lac Marmont sector deposits are commonly poor in these elements. Deposits occur in or are closely associated with 1175–1168 Ma leucogranite. They contain combinations of magnetite, clinopyroxene, blue–green hornblende, titanite, apatite, fluorite, quartz, biotite, andradite, epidote, albite, hematite, sulfides (chalcopyrite, pyrite, pyrrhotite, molybdenite, sphalerite), ilmenite, allanite, and other REE-bearing minerals. Veins and breccias are common. Most of the magnetite mineralization was preceded by potassic metasomatism (microcline) and was followed by most of the sulfides and radioactive minerals. Nearby sulfide-dominant deposits may be related. The deposits were formed by metasomatic replacement and fracture filling from hydrothermal fluids of variable composition, which were probably channeled in major, active faults. Oxygen-isotope data from magnetite-rich rocks suggest that fluids were predominantly magmatic and (or) metamorphic and that, locally, mixing with cooler meteoric water may have facilitated precipitation of sulfides and rare-metal minerals. Titanites in mineralized rock have been dated at 972 ± 5 Ma, but most magnetite may be older. Mineralization was syn- to post-tectonic and occurred in an orogenic to orogenic-collapse setting. The Cu–REE–Y-rich deposits are similar to iron oxide – copper – gold (IOCG) Olympic Dam type deposits, and copper- and rare-metals-poor occurrences resemble magnetite ± apatite Kiruna-type deposits.
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30

Soloviev, Serguei G., Sergey G. Kryazhev, Vadim S. Kamenetsky, Vasily N. Shapovalenko, Svetlana S. Dvurechenskaya, Alexei V. Okulov, and Konstantin I. Voskresensky. "The Ulandryk and related iron oxide-Cu-REE(-Au-U) prospects in the Russian Altai: A large emerging IOCG-type system in a Phanerozoic continental setting." Ore Geology Reviews 146 (July 2022): 104961. http://dx.doi.org/10.1016/j.oregeorev.2022.104961.

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31

Baidya, Abu Saeed, Dipak Chandra Pal, and Dewashish Upadhyay. "Biotite chemistry and mineral association as an indicator of redox conditions in the iron oxide Cu-Au (IOCG) system: Constraints from the Khetri Copper Belt, western India." Ore Geology Reviews 139 (December 2021): 104544. http://dx.doi.org/10.1016/j.oregeorev.2021.104544.

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32

SARLUS, ZMAR, ULF B. ANDERSSON, TOBIAS E. BAUER, CHRISTINA WANHAINEN, OLOF MARTINSSON, ROGER NORDIN, and JOEL B. H. ANDERSSON. "Timing of plutonism in the Gällivare area: implications for Proterozoic crustal development in the northern Norrbotten ore district, Sweden." Geological Magazine 155, no. 6 (April 27, 2017): 1351–76. http://dx.doi.org/10.1017/s0016756817000280.

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AbstractZircon ion probe (secondary-ion mass spectrometry or SIMS) data from a set of intrusive rocks emplaced in the vicinity of major ore bodies, as well as from large igneous intrusions in the Gällivare area, gave the following results: (1) the Dundret ultramafic–mafic layered complex (1883±5 Ma), the Aitik granite (1883±5 Ma), the Nautanen diorite (1870±12 Ma), the Vassaravaara ultramafic–mafic layered complex (1798±4 Ma), the Aitik dolerite (1813±9 Ma), the Bergmästergruvan and Sikträsk syenites (1795±4 Ma and 1801±3 Ma, respectively) and the Naalojärvi granite (1782±5 Ma). These data broadly fall within the ranges 1.89–1.87 Ga (early Svecofennian) and 1.80–1.78 Ga (late Svecofennian), but geochronologically allow further subdivision into pulses at 1885–1880, 1875–1870, 1800 and 1780 Ma. During these events, large layered ultramafic–mafic and felsic plutonic rocks were generated with distinct overlap in time suggesting coeval felsic–mafic magmatism. Results also indicate the presence of inheritedc.1.87 Ga zircon crystals in the plutonic rocks at 1.78 Ga, supporting reworking of the previous crust. These data indicate the importance of mantle-derived mafic underplating in the process of crustal magma generation in the region. Thec.1.88 Ga event that generated ultramafic–mafic layered complexes is tentatively suggested to have played an important role in the formation of the Aitik Cu–Au porphyry system. The later event atc.1.80 Ga, generating voluminous mafic–felsic units, is suggested to be coupled to the regional iron-oxide-copper-gold (IOCG) overprint.
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33

Liang, Pei, Yu Zhang, and Yuling Xie. "Chemical Composition and Genesis Implication of Garnet from the Laoshankou Fe-Cu-Au Deposit, the Northern Margin of East Junggar, NW China." Minerals 11, no. 3 (March 23, 2021): 334. http://dx.doi.org/10.3390/min11030334.

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In order to reveal the formation mechanism of different garnets and its implications for the fluid evolution in the Laoshankou Fe-Cu-Au deposit in the northern margin of East Junggar (NW China), three types of garnet have been investigated in detail in this study. (1) Type 1 grossular, formed at Ca-silicate stage (stage I, the pre-mineralization stage), was replaced by Type 2 garnet and magnetite, and displays a compositional range of Grs44–53Adr44–53, which has relatively lower total REE (rare earth elements) contents (8.14–32.8 ppm) and markedly depleted LREE (light rare earth elements) with distinctive positive Eu anomaly (1.36–9.61). (2) Type 2 Al-rich andradite, formed at the early sub-stage of amphibole-epidote-magnetite stage (stage II, the main magnetite mineralization stage), can be divided into two sub-types, i.e., Type 2a and Type 2b. Type 2a garnets exhibit polysynthetic twinning and relatively narrow compositional variations of Adr63–66Grs31–34 with HREE-(heavy rare-earth elements) enrichment and positive Eu anomalies (3.22–3.69). Type 2b garnets own wide compositional variations of Adr55–77Grs21–43 with relatively higher REE contents (49.1–124 ppm), markedly depleted LREE and a distinctive positive Eu anomaly (2.11–4.61). (3) Type 3 andradite (Adr>91) associated with sulfide stage (stage III, the main copper-gold mineralization stage) is different from other types of garnets in Laoshankou, which are characterized by lowest total REE contents (1.66–91.1 ppm), flat HREE patterns, LREE-enrichment and the strongest positive Eu anomalies (3.31–45.48). Incorporation of REE into garnet is largely controlled by external factors, such as fluid chemistry, pH, ƒO2 and water-rock ratios as well as its crystal chemistry. Type 1 and 2 garnets mainly follow the creation of X2+ (e.g., Ca2+) site vacancy, e.g., [X2+]−3VIII[]+1VIII[REE3+]+2VIII. The REE3+ substitution mechanism for Type 3 garnet is the Na+-REE3+ coupled substitutions, e.g., [X2+]−2VIII[X+]+1VIII[REE3+]+1VIII, without the evaluation of the creation of site vacancy. The compositional variations from Type 1 to Type 3 garnet indicate significant differences of fluid compositions and physicochemical conditions, and can be used to trace the fluid–rock interaction and hydrothermal evolution of garnet. Type 1 grossular was formed by magmatic fluid under low water–rock ratios and ƒO2, and neutral pH environment by diffusion metasomatism in a nearly closed system with the preferential incorporation into the grossular of HREE. As the long fluid pore residence and continuing infiltration metasomatism under nearly closed-system conditions, fluids with high water/rock ratios were characterized by increased ƒO2, more active incorporation of Fe3+ and REE, and formed Type 2 Al-rich andradite. In contrast, Type 3 garnet formed by oxidizing magmatic fluid under a mildly acidic environment with highest ƒO2 and water–rock ratios, and was influenced by externally derived high salinity and Ca-rich fluids in an open system. Thus, the geochemical features of different types and generations of garnets in the Laoshankou deposit can provide important information of fluid evolution, revealing a transition from neutral magmatic fluid to oxidizing magmatic fluid with addition of external non-magmatic Ca-rich fluid from the Ca-silicate stage to the sulfide stage. The above proved the fluid evolution process further indicates that the Laoshankou deposit prefers to be an IOCG-like (iron oxide-copper-gold) deposit rather than a typical skarn deposit.
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34

Van, H. Duong, C. Nguyen Dinh, A. Piestrzyński, and J. Pieczonka. "Relationship between Selected Major, Minor, and Trace Elements in Iron Oxide–Copper–Gold Deposits, an Example from the Unique Sin Quyen Deposit (Lào Cai Province, North Vietnam)." Russian Geology and Geophysics, May 5, 2021. http://dx.doi.org/10.2113/rgg20194156.

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Abstract —We study the relations between several selected elements present in the Sin Quyen IOCG deposit, Lào Cai, North Vietnam, and interpret the obtained correlations, especially with a coefficient higher than 0.7. The correlations with high coefficients are mainly observed for the elements belonging to the chalcophile group (Cu, Ag, Au, Te, and Bi) and for the relation between uranium and Ag, Au, Cu, Pb, and Bi. Although the S-, Fe-, and REE-bearing minerals are predominant in the studied deposit, no strong correlation between them and the other elements was observed, even with Cu. The phenomena are primarily explained based on the geochemical properties of the mentioned elements and the characteristics of IOCG deposits.
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35

Li, Jianping, Huayong Chen, Weihua Liu, Xing Ding, Richen Zhong, and Chang Yu. "Copper mobilization via seawater-volcanic rock interactions: new experimental constraints for the formation of the iron oxide Cu-Au (IOCG) mineralization." Geochimica et Cosmochimica Acta, June 2022. http://dx.doi.org/10.1016/j.gca.2022.06.004.

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36

Steadman, Jeffrey A., Karsten Goemann, Jay M. Thompson, Colin M. MacRae, Ivan Belousov, and Max Hohl. "Hyperspectral cathodoluminescence, trace element, and U-Pb geochronological characterization of apatite from the Ernest Henry iron oxide copper-gold (IOCG) deposit, Cloncurry district, Queensland." Frontiers in Earth Science 10 (October 4, 2022). http://dx.doi.org/10.3389/feart.2022.926114.

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Hyperspectral cathodoluminescence (CL), geochemical, and geochronological characterization of a series of apatite-bearing samples from within and around the Ernest Henry IOCG deposit, NW Queensland, Australia, have revealed complex mineral parageneses and a spectrum of U-Pb ages that point to the effects of multiple geological processes. No two samples are identical, either in geochemistry or texture, despite their relative proximity to one another (all samples within 5 km from Ernest Henry). Hyperspectral CL maps reveal diverse internal textures and emissions ranging from near infrared (NIR) to near ultraviolet (UV) with a complex series of spectra in all samples, requiring the fitting more than 40 individual peaks (both sharp and broad) to capture the observed variability. Imaging analyses via LA-ICPMS show that apatite from the Ernest Henry district is enriched above background in a variety of trace elements, including Na, Mg, Al, Si, V, Mn, As, Sr, Y, the rare Earth elements (REEs), Pb, Th, and U. Samples outside the ore zone display chondrite-normalized REE profiles that are consistent with either a magmatic or hydrothermal origin, whereas ore zone apatite exhibits profiles that are decidedly hydrothermal in nature. Moreover, specific zones within ore zone apatite grains are very As-rich (up to 7 wt% As2O5), and the effect of such high As on the hyperspectral CL signature of these zones is a pronounced dampening of CL emission, regardless of REE concentrations. Uranium-Pb dating of the same samples (via LA-ICPMS) has yielded a diverse array of overlapping Mesoproterozoic ages ranging from 1,580 ± 34 Ma to 1,533 ± 61 Ma. These results correlate to published ages that constrain hydrothermal alteration in the Ernest Henry area, both before and during Cu-Au mineralization. Collectively, these data highlight the complexity of apatite studies at Ernest Henry, the broader Cloncurry district, and probably analogous terranes elsewhere. A combination of micro-scale methods such as those used in this study are shown to be essential for accurately deciphering geological information contained within petrogenetic indicator minerals.
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