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  • 1
    Publication Date: 2012-12-20
    Description: The ~3240 Ma Panorama volcanic-hosted massive sulfide (VHMS) district is unusual for its high degree of exposure and low degree of postdepositional modification. In addition to typical seafloor VHMS deposits, this district contains greisen- and vein-hosted Mo-Cu-Zn-Sn mineral occurrences that are contemporaneous with VHMS orebodies and are hosted by the Strelley granite complex, which also drove VHMS circulation. Hence the Panorama district is a natural laboratory to investigate the role of magmatic-hydrothermal fluids in VHMS hydrothermal systems. Regional and proximal high-temperature alteration zones in volcanic rocks underlying the VHMS deposits are dominated by chlorite-quartz ± albite assemblages, with lesser low-temperature sericite-quartz ± K-feldspar assemblages. These assemblages are typical of VHMS hydrothermal systems. In contrast, the alteration assemblages associated with granite-hosted greisens and veins include quartz-topaz-muscovite-fluorite and quartz-muscovite (sericite)-chlorite-ankerite. These vein systems generally do not extend into the overlying volcanic pile. Fluid inclusion and stable isotope studies suggest that the greisens were produced by high-temperature (~590°C), high-salinity (38–56 wt % NaCl equiv) fluids with high densities (〉1.3 g/cm 3 ) and high 18 O (9.3 ± 0.6 ). These fluids are compatible with the measured characteristics of magmatic fluids evolved from the Strelley granite complex. In contrast, fluids in the volcanic pile (including the VHMS ore-forming fluids) were of lower temperature (90°–270°C), lower salinity (5.0–11.2 wt % NaCl equiv), with lower densities (0.88–1.01 g/cm 3 ) and lower 18 O (–0.8 ± 2.6 ). These fluids are compatible with evolved Paleoarchean seawater. Fluids that formed the quartz-chalcopyrite-sphalerite-cassiterite veins, which are present within the granite complex near the contact with the volcanic pile, were intermediate in temperature and isotopic composition between the greisen and volcanic pile fluids (T = 240°–315°C; 18 O = 4.3 ± 1.5 ) and are interpreted to indicate mixing between the two end-member fluids. Evidence of mixing between evolved seawater and magmatic-hydrothermal fluid within the granite complex, together with the lack of evidence for a magmatic component in fluids from the volcanic pile, suggest partitioning of magmatic-hydrothermal from evolved seawater hydrothermal systems in the Panorama VHMS system. This separation is interpreted to result from either the swamping of a relatively small magmatic-hydro-thermal system by evolved seawater or density contrasts precluding movement of magmatic-hydrothermal fluids into the volcanic pile. Variability in the salinity of fluids in the volcanic pile, combined with evidence for mixing of low- and high-salinity fluids in the massive sulfide lens, is interpreted to indicate that phase separation occurred within the Panorama hydrothermal system. Although we consider this phase separation to have most likely occurred at depth within the system, as has been documented in modern VHMS systems, the data do not allow the location of the inferred phase separation to be determined.
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  • 2
    Publication Date: 2016-02-23
    Description: Gold production from the northern Pataz district in the eastern Andean Cordillera of Peru has been sourced mainly from mesothermal quartz-carbonate-sulfide veins hosted by the Mississippian Pataz batholith. Gold is also found in basement-hosted veins underlying the batholith, in the Vijus-Santa Filomena area of the district. Both are located within a central horst; similar vein mineralogy and proximal phengitic white mica alteration are common to both. However, comb-textured quartz, the chemical compositions of bulk ore and sulfide minerals, and the presence of barite and siderite veins suggest that the basement-hosted veins formed at a shallower crustal level. Similar expressions of hydrothermal alteration associated with anomalous gold, As, Sb, and Tl are also present in the adjacent Lavasen graben, where alteration is intimately associated with volcanic processes that deposited the Mississippian Lavasen Volcanics. K-Ar and 40 Ar- 39 Ar ages for hydrothermal illite from all three locations range between Mississippian and Late Triassic but are consistent with a single Mississippian hydrothermal event, if the data record a minimum age for original illite formation. The geologic setting, mineralization styles, and chemical data suggest a range of crustal depths, ranging from mesothermal batholith-hosted veins through shallow to intermediate depths for the Vijus-Santa Filomena area to a near-surface epithermal setting for the Misquichilca area. Telescoping of this 10- to 13-km crustal range into a 3-km topographic section of the Andes is attributed to syn- and postmineralization uplift and erosion. Sulfide-rich high-grade ore shoots and moderately saline fluid inclusions in the batholith-hosted veins are inconsistent with the original orogenic gold model and suggest a magmatic source component for the ore fluid, consistent with stable isotope (O, H, C, and S) compositions of quartz, illite, carbonates, and sulfides. The isotopic data suggest a mixed magmatic-meteoric ore fluid in the basement-hosted deposits of the Vijus-Santa Filomena area and the volcanic-hosted Misquichilca area. Both the Pataz batholith and the Esperanza Subvolcanic Complex are of the same Mississippian age as the hydrothermal alteration and mineralization. The Esperanza Subvolcanic Complex, comagmatic with the Lavasen Volcanics, contains cognate mineral clots from which a subjacent magma chamber can be inferred. It exhibits potassic, calc-silicate, and argillic alteration, and evidence for the evolution of an Fe-rich volatile phase. The Lavasen-Esperanza magma suite is ferroan and weakly alkaline, with A-type affinities. These features provide a conceptual genetic link with hydrothermal alteration associated with gold mineralization, including Fe (±As) sulfides, phengitic white mica, celadonite, Fe-rich carbonates, and less common Fe oxides. An oxidized intrusion-related model is proposed for gold and hydrothermal alteration in the northern Pataz district.
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  • 3
    Publication Date: 2012-06-01
    Description: The banded iron formation (BIF)-hosted iron ore deposits in the lower greenstone succession of the Koolyanobbing greenstone belt, 50 km north of Southern Cross in Western Australia, are a ~200 Mt high-grade Fe (〉58%) pre-mining resource and represents one of the most important iron ore districts in the Yilgarn craton. Four hypogene alteration (ore-forming) stages and one supergene upgrading event took place: (1) During ore stage 1, LREE-depleted, transition metal-enriched, Mg-Fe (±Ca) carbonates replaced quartz in BIFs. The deposit-scale alteration was most likely induced by devolatilization of sea-floor–altered, Ca-Si–depleted mafic rocks in the vicinity of the BIF during early regional (syn-D1), very low to low-grade metamorphism and was most strongly developed on reactivated BIF-basalt contacts. (2) Ore stage 2 involved the formation of patchy magnetite ore by a syn-D2 to -D4 dissolution of early carbonate. Enrichment of Fe2O3total in magnetite iron ore was by a factor of 2 to 2.4, and compatible trace elements in magnetite, such as Ga, V, and Al, were immobile. A subdeposit-scale ferroan talc-footprint proximal to magnetite iron ore in the largest deposit (K deposit) was associated with ore stage 2 and resulted from dissolution of magnesite due to reaction with silica in the BIF under greenschist facies conditions and potentially high fluid/rock ratio. (3) Magnetite growth, during ore stage 3, forming granular magnetite-martite ore is related to a subsequent hydrothermal event, occurring locally throughout the belt, especially in D2b faults. (4) Ore stage 4 was associated with Fe-Ca-P-(L)REE-Y–enriched hydrothermal fluids, possibly from a magmatic source such as the postmetamorphic Lake Seabrook granite that crops out about 10 km west of the Koolyanobbing deposits and at the southern margin of the greenstone belt. These Ca-enriched fluids interacted with distal metamorphosed mafic rock and influenced the BIF-ore system in a small number of deposits. They were channelled through regional D4 faults and caused specularite-dolomite-quartz alteration, resulting in Fe grades of up to 68%. (5) Supergene upgrade (ore stage 5) by (further) gangue leaching in the weathering zone was most effective in carbonate-altered BIFs and magnetite ore. This process, together with supergene martitization and goethite replacement of magnetite, led to the formation of high-grade, locally (at K deposit) high P goethite-martite ore. At Koolyanobbing, the two geochemically distinct stages of Archean carbonate alteration clearly controlled the formation of hypogene magnetite-specularite-martite–rich ore and recent supergene modification, including the further upgrade of Fe ore.
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  • 4
    Publication Date: 2012-06-01
    Description: Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) image analysis is a proven method for mapping mineral and geochemical zonation associated with a variety of ore types, including orogenic Au, porphyry Cu-(Mo), porphyry-skarn, Pb-Zn-Au, and Mn systems. Only recently has this technique been applied, in a general sense, to mineral alteration mapping and exploration for Fe ore deposits hosted by banded iron formations (BIFs). For this reason, the Archean Weld Range greenstone belt that hosts the Beebyn and Madoonga Fe ore deposits has been chosen as a case study area to test the effectiveness of ASTER imaging techniques for the identification of Fe orebodies. Banded iron formations in the Weld Range district crop out as a series of parallel, 10- to 500-m-wide, 55 wt % Fe) iron ore deposits host Archean hypogene magnetite and specular hematite orebodies that are locally replaced by more recently formed, supergene goethite-hematite ore within several hundred meters of the present erosion surface. A common feature of all ore types hosted by BIFs is a high Fe content relative to SiO2. Consequently, all types of Fe ore in the Weld Range district are best identified by the ferric iron to silica index and the opaques to silica index, for the reason that these ASTER image products detect surfaces that are rich in (opaque) Fe oxide minerals and have a low silica abundance. Gabbro, dolerite, and basalt country rocks located within 20 m of high-grade Fe ore zones in BIFs are altered to hypogene Fe-rich chlorite and, more rarely, are altered by Fe-rich talc. These hypogene alteration zones are best detected by the ferrous iron content in MgOH minerals and carbonates and the FeOH group abundance products, which identify hypogene Fe chlorite and Fe talc. This study demonstrates that integrated remote spectral sensing techniques (ASTER, airborne hyperspectral, and radiometric) used in conjunction with geophysical surveys (aeromagnetic and gravity) are useful for district-scale exploration for Fe orebodies hosted by BIFs. The spectral sensing techniques are a rapid, cost-effective, and efficient means for generating and ranking exploration targets that are located in areas with restricted physical access.
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  • 5
    Publication Date: 2018
    Description: 〈span〉〈div〉Abstract〈/div〉The Karouni orogenic gold deposits are located in north-central Guyana 35 km to the west of the 5 Moz Omai gold deposit. They are hosted in a 2200 to 2100 Ma greenstone belt within the Paleo- to Neoproterozoic Guiana Shield. Karouni consists of two deposits, Smarts and Hicks, located 2 km apart along the NW-striking Smarts-Hicks shear zone. Both deposits are hosted within a sequence of greenschist facies mafic volcanic rocks and felsic intrusions. The hydrothermal alteration mineral assemblages vary according to lithology and are characterized by narrow selvages (〈1–4 m in width). A chlorite-talc-calcite assemblage dominates in high MgO basalt, whereas in high TiO〈sub〉2〈/sub〉 dolerite a progression toward the vein is seen from chlorite-calcite-rutile- to albite-dominated mineralogy. Karouni is anomalous among orogenic gold deposits for its dominant sodic alteration and distinct lack of potassic alteration. Gold is located within inclusions in coarse, disseminated pyrite associated with the proximal alteration zones and as coarse native gold within the quartz-carbonate veins. Minor gold is also located within Au-bearing telluride minerals. The high TiO〈sub〉2〈/sub〉 dolerites formed a favorable chemical trap due to their high magnetite content, suggesting sulfidation via redox reaction as a possible mechanism of gold deposition. Mass balance modeling of the hydrothermal alteration indicates a wall rock-dominated system with limited addition or subtraction of major elements with the exception of C, S, and Na. Modeling of the proximal alteration has also shown strong trace element enrichment of W-Bi-Ag-Te-Mo-Pb, all of which are correlative with gold. In situ laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) trace element geochemistry and secondary ion mass spectrometry (SIMS) S isotope analyses of pyrite from the gold-bearing hydrothermal system within the deposit indicate a geochemically and isotopically homogeneous system with only minor trace element variation due to differences in host rock, suggesting a single hydrothermal pulse correlative with the late stages of the Trans-Amazonian orogeny.〈/span〉
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  • 6
    Publication Date: 2018
    Description: 〈span〉〈div〉Abstract〈/div〉The Karouni orogenic gold deposit is located in north-central Guyana, 35 km to the west of the 5 Moz Omai gold mine. The deposit is hosted within 2.2 to 2.1 Ga volcano-sedimentary rocks of the Barama-Mazaruni Supergroup, part of the Paleo- to Neoproterozoic Guiana Shield. Karouni consists of two zones, Smarts and Hicks, located 2 km apart along the NW-striking Smarts-Hicks shear zone, a second-order splay of the regional-scale Makapa-Kuribrong shear zone. The Karouni camp is composed of a lower sequence of mafic volcanic rocks, overlain by a lower sequence of immature sandstone and conglomerate, and an upper sequence of sandstone and laminated carbonaceous siltstone, intruded by several generations of felsic plutons and dikes. Whole-rock geochemical analysis indicates their formation in oceanic island-arc environment, and mantle-like characteristics of the high MgO basalts may indicate the presence of deep-seated structures during the early history of the camp. Regional-scale deformation during the Trans-Amazonian orogeny led to tectonic inversion of the volcano-sedimentary basins, greenschist facies metamorphism, and the development of strike-slip shear zones. Late movement on these shear zones is interpreted to be responsible for hydrothermal fluid flow, alteration, and gold mineralization within the Karouni gold camp. The Smarts and Hicks orebodies are localized within dilatational bends formed at changes in strike of the Smarts-Hicks shear zone during late dextral transcurrent movement. Rheological contrast played a dominant role in the formation of the deposits with shear-hosted, NW-striking, and steeply dipping quartz-carbonate-chlorite ± tourmaline-pyrite-gold (V〈sub〉2a〈/sub〉) veins preferentially hosted in ductilely deformed, high MgO basalts, whereas mineralized N-S, quartz-carbonate-chlorite ± tourma-line-pyrite-gold (V〈sub〉2b〈/sub〉) veins are hosted within rheologically competent high TiO〈sub〉2〈/sub〉 dolerite sills and granodiorite dikes. The interaction of these structures with favorable lithology is key for localizing high-grade orebodies.〈/span〉
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  • 7
    Publication Date: 2016-05-24
    Description: The Neoproterozoic Telfer deposit, one of Australia’s largest gold-copper deposits, is located in the Paterson orogen. Several highly differentiated calc-alkaline to alkali-calcic peraluminous granites intruded the metasedimentary rocks near (5–20 km) Telfer contemporaneously with structurally controlled gold-copper mineralization. Fluid inclusion assemblages with different fluid inclusion types were identified in samples from a range of different vein types. These inclusion types range from three-phase aqueous L aq + V aq + S halite , high-salinity (≤50 wt % NaCl equiv), high-temperature (≤460°C) inclusions to two-phase aqueous or two-phase aqueous carbonic, low- to moderate-salinity (2–22 wt % NaCl equiv), moderate- to high-temperature (≤480°C) fluid inclusions. Fluid inclusion trapping mechanisms and interpreted precipitation mechanisms for gold and copper include (1) adiabatic cooling between 450° and 200°C in all veins and, (2) locally, fluid phase separation at about 300°C. The trapping pressure of fluid inclusion assemblages trapped during phase immiscibility was calculated to be approximately 1.5 kbar. For fluid inclusion assemblages that lack evidence for phase immiscibility, a pressure at the temperature of final homogenization of up to 3 kbar was calculated. This high pressure value is interpreted to be related to local fluid overpressure, as a consequence of fault zone movement, in faults and fractures that localized gold at Telfer. Phase immiscibility and gold precipitation were induced during sharp pressure decrease accompanying fault zone movement. In situ laser inductively coupled plasma-mass spectrometry (ICP-MS) analyses of fluid inclusions revealed high trace element contents in all fluid inclusion assemblages. Manganese/Fe ratios of 〈0.24 in all vein types suggest that reduced fluids dominated the system, but, locally, a switch to more oxidized conditions with Mn/Fe ratios 〉0.24 is observed. Given the high temperatures and salinities of up to 480°C and 42 wt % NaCl equiv, Au and Cu were likely transported as chloride complexes. This interpretation is supported by the observation that the highest base metal contents occur in the highest-salinity fluid inclusion. Potassium/Ca ratios of 〉1 in most assemblages, the high homogenization temperatures (≤480°C) in many fluid inclusion assemblages, and the high trace element contents (e.g., Fe, Mg, K, Na) in most of the fluid inclusion assemblages are compatible with involvement of a magmatic hydrothermal fluid during gold-copper mineralization. This fluid was probably derived from the coeval granites in the Telfer area and, thus, Telfer is interpreted to be a distal, intrusion-related, metasedimentary rock-hosted, gold-copper deposit type.
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  • 8
    Publication Date: 2013-05-03
    Description: The Serra Norte Carajás banded iron-formation (BIF)-hosted iron ore deposits are located in the Carajás mineral province. The deposits are hosted in the ca. 2.7 Ga Grão Pará Group, a metamorphosed volcanic-sedimentary sequence where jaspilites are under- and overlain by basalts, both at greenschist facies conditions. They represent one of the largest high-grade (〉60 wt % Fe) BIF iron ore deposits and resources in the world, with hypogene iron mineralization considered to be Paleoproterozoic. Four main open pits have, to date, produced about 1.2 billion metric tons (Bt) of high-grade iron ore with additional resources of 10 Bt. Ore types at the Serra Norte deposits include soft and hard ore; the latter consists of banded, massive and/or brecciated ores and is mainly localized along the contact with the surrounding hydrothermally altered basalts. Distinct hydrothermal alteration zones consist of veins and breccias that surround the hard ores, including: (1) an early alteration zone (distal portion of orebodies), characterized by recrystallization of jasper, formation of magnetite (± martite), and the local introduction of quartz and carbonate-sulfide (±quartz) veins; (2) intermediate alteration, synchronous with the main iron ore-forming event, which is accompanied by widespread development of martite, quartz-hematite and hematite-quartz veins, and dissolution of carbonate; and (3) proximal alteration zone having various types of hard and hard-porous hematite ores containing microplaty, anhedral, euhedral, and tabular hematite species. Locally, high-grade breccia ores contain dolomite and kutnahorite matrices indicating carbonate introduction. High-grade ore zones contain quartz ± carbonate-hematite veins and breccias. Combined microthermometry, iron chromatography, and in situ laser ablation ICP-MS analyses on fluid inclusion assemblages from five vein types reveal that (1) early alteration vein-breccia quartz-carbonate contains high-salinity (up to 30 equiv wt % NaCl) fluid inclusions, with Ca, besides Na, K, and Mg, which were trapped at temperatures of 220° to 320°C. The quartz-hosted fluid inclusions have a wide range of Cl/Br ratios, presence of Li, base metals Cu-Pb-Zn, and Fe; (2) intermediate alteration vein quartz contains both low-salinity (Na-Fe-Mg-rich) and high-salinity (Ca-Mg-Fe-rich) fluid inclusions, with trapping temperatures of 210° to 290°C; (3) advanced alteration vein and breccia quartz-carbonate has low- to high-salinity fluid inclusions and trapping temperatures between 240° to 310°C, with the low-salinity inclusions being much more abundant in quartz. There is a gradual dilution of the metals signature in fluid inclusions from early to late- and/or advanced-stage veins and breccias. The large amount of Ca in the fluid inclusions is compatible with extensive exchange of the hydrothermal fluids with the surrounding chloritized-hematitized metabasaltic wall rock. Oxygen isotope analyses on different oxide species reveal that the heaviest 18 O SMOW values, up to 15.2, are recorded for jaspilites, followed by magnetite, between –0.4 to +4.3, and then by different hematite species such as microplaty, anhedral and tabular, which fall in the range of –9.5 to –2.4. These results show a progressive depletion in 18 O values from the earliest introduced hydrothermal oxide magnetite toward the latest tabular hematite. The advanced alteration stage in high-grade ore displays the most depleted 18 O values and represents the highest fluid/rock ratio during hydrothermal alteration. This depletion is interpreted to result from the progressive mixture of descending, heated meteoric water with ascending modified magmatic fluids. Sulfides from the distal zone of metabasaltic rocks have 34 S values close to 0, consistent with a magmatic origin for the sulfur. Heavier 34 S values, of up to 10.8, in vein sulfides hosted in jaspilite, may reflect interaction with meteoric waters or, alternatively, variations in f O 2 and pH conditions during evolution of the hydrothermal fluid. Calcite-kutnahorite 13 C and 18 O values from the distal alteration zones show a large 13 C range of –5.5 to –2.4 and a relatively narrow 18 O range of 9.3 to 11.7. However, dolomite matrix breccias from the advanced hydrothermal zone, i.e., ore, exhibit a wider 18 O range from 15.1 to 21.8 and a more restricted 13 C range from –5.0 to –3.9. This latter range points to a single carbon source, of possible magmatic nature, whereas the larger 18 O range suggests multiple carbon and oxygen sources. The 87 Sr/ 86 Sr ratios for carbonates from the distal and advanced hydrothermal zones range between 0.7116 to 0.7460, suggesting incorporation of strontium from multiple crustal sources, including magmatic-hydrothermal fluids. A dual magmatic-meteoric hydrothermal fluid-flow model is proposed for the hematite ores in which an early, low Cl/Br ratio, saline, ascending modified magmatic fluid, caused widespread oxidation of magnetite to hematite. Progressive influx of light 18 O meteoric water, mixing with the ascending magmatic fluids, is interpreted to have been initiated during the intermediate stage of alteration. The advanced and final hydrothermal stage was dominated by a massive influx of low-salinity meteoric water, which maintained intermediate temperatures of 240° to 310°C, and concomitant formation of the paragenetically latest tabular hematite. The giant Carajás iron deposits are unique in their setting within an Archean granite-greenstone belt and their modified magmatic-meteoric hydrothermal system, compared to the other two end-member BIF iron deposit types, namely the basin-related Hamersley type and the metamorphosed metasedimentary- basin-related Iron-Quadrangle-type. The distinct hydrothermal alteration signature present in both wall-rock basalts and jaspilites, in combination with distinct fluid chemistry signatures, particularly the low 18 O values of paragenetically late oxides indicative of massive influx of meteoric water into the high-grade orebodies, provide distinctive parameters for defining the Carajás end-member type BIF deposit class.
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  • 9
    Publication Date: 2014-07-10
    Description: High-grade iron ore of the 4EE orebody of the 4E deposit (〉200 Mt at 63.5 wt % Fe) occurs as a southerly dipping sheet within banded iron formation (BIF) of the Paleoproterozoic Dales Gorge and Joffre members of the Brockman Iron Formation. Structural reconstruction of the 4E deposit shows that reactivation of the 18E fault and development of the NW-striking, steeply SW dipping 4E and 4EE normal faults resulted in preservation of the 4EE orebody below the 4E deposit, and 400 m below the modern topographic surface. Three hypogene alteration zones between low-grade BIF and high-grade iron ore are observed: (1) distal magnetite-quartz-dolomite-stilpnomelane-hematite ± pyrite, (2) intermediate magnetite-dolomite-hematite-chlorite-quartz-stilpnomelane, and (3) proximal hematite-dolomite-chlorite ± pyrite ± magnetite. Hydrothermal alteration is temporally and spatially constrained by NW-trending dolerite dikes that intruded the 4E and 4EE faults prior to hypogene alteration. Six vein types (V 1 –V 6 ) are recognized at the 4E deposit. The veins both cut and parallel the primary BIF layers and were emplaced contemporaneously with the hydrothermal alteration zones that record the transformation of low-grade BIF to high-grade iron ore. Our integrated structural-hydrothermal alteration and fluid flow model proposes that during early stage 1a, hypogene fluid flow in the 4E orebody occurred during a period of continental extension and enhanced heat flow within sedimentary basins to the south of the Paraburdoo Range. Heated basinal brines were focused by the NW-striking, steeply SW dipping 4E and 4EE normal faults and reacted with BIF of the Dales Gorge and Joffre members. The warm to hot (160°–255°C), Ca-rich (26.6–31.9 equiv wt % CaCl 2 ) basinal brine interacted with magnetite-chert layers, transforming them into magnetite-quartz-dolomite-stilpnomelane-hematite-pyrite BIF. The iron-rich brine (up to 2.8 wt % Fe) likely originated from evaporated seawater that had lost Mg and Na and gained Li and Ca through fluid-rock reactions with volcaniclastic rocks and carbonate successions within the Wittenoom Formation. The first incursion of deeply circulating, low-salinity (5.8–9.5 wt % NaCl equiv), heated (106°–201°C) modified meteoric water is recorded in late stage 1a minerals. This modified meteoric water had lost some of its Na through wall rock interaction with plagioclase, possibly by interaction with dolerite of the Weeli Wooli Formation that directly overlies the Joffre and Dales Gorge members. Stage 1b involved continuing reactions between the hydrothermal fluids and the magnetite-quartz-dolomite-stilpnomelane-hematite-pyrite BIF, and produced both the intermediate magnetite-dolomite-hematite-chlorite-pyrite and the proximal hematite-dolomite-magnetite-stilpnomelane alteration assemblages. Microplaty (10–80 μ m), platy (100–250 μ m), and anhedral hematite increasingly replace magnetite in the intermediate alteration zone, forming the proximal alteration zones that consist of microplaty, platy, anhedral hematite and magnetite. The intermediate and proximal alteration zones represent the mixing of a hot (250°–400°C), high-salinity, Ca-rich (30–40 wt % CaCl 2 equiv), Sr-rich basinal brine with low-temperature and low-salinity (~5 wt % NaCl equiv) modified meteoric water that was heated (~100°–200°C) during its descent into the upper crust. Heterogeneous mixing of the two end-member fluids resulted in the trapping of primary fluid inclusion assemblages containing a wide range of trapping temperatures (up to 200°C) and salinities (up to 25 wt % NaCl equiv). Stage 1c of the hypogene hydrothermal fluid is characterized by low-temperature (〈110°C), low-salinity (~5 wt % NaCl) meteoric water that interacted with the proximal hematite-dolomite-magnetite-stilpnomelane–altered BIF, leaving a porous, hematite-apatite high-grade ore. Supergene alteration affected the orebody since the Cretaceous and produced a hematite-goethite alteration assemblage, resulting in destruction of the hypogene alteration zones that are only preserved below the depth of modern weathering. Discovery of the concealed 4EE orebody of the 4E deposit demonstrates that structural geology plays a critical role in the exploration for high-grade iron orebodies. Structural reconstruction should be considered a critical exploration activity in structurally complex terranes where concealed orebodies may exist.
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  • 10
    Publication Date: 2012-08-01
    Description: The high-grade Flying Fox komatiite-hosted Ni sulfide deposit, located in the Forrestania greenstone belt of the Archean Yilgarn Craton, Western Australia, is hosted in a deformed and metamorphosed volcano-metasedimentary succession. Postmineralization events have sheared and modified the texture and composition of the original massive sulfide ore, creating up to 11 distinct ore shoots including massive, stringer/vein, and breccia sulfides composed of pyrrhotite, pentlandite, chalcopyrite, and variable abundances of pyrite ranging up to 40 vol %. Nickel and platinum group elements (PGE) tenor variations were investigated in two ore shoots, T4 and T5. All mineralization styles show considerable variability in Ni tenor. PGEs show strong linear correlations between Ir, Os, Ru, and Rh, but poor correlation between Pt, Pd, and Cu. The normalized molar proportions of Fe, Ni, and S, projected into the Fe-Ni-S ternary system, show a distinct linear trend of pyrite addition to a typical primary magmatic composition and no correlation with mineralization style. The high pyrite content present throughout the Flying Fox ore is also associated with elevated Cu and As contents and is interpreted to be primarily due to the addition of pyrite from circulating Fe-, S-, Cu-, and As-enriched fluids creating pyrite-pentlandite intergrowths. Localized mechanical segregation of pyrite, sulfidation of pyrrhotite to pyrite, and oxidation of pyrrhotite to pyrite + magnetite has also contributed to these increased pyrite contents, although to a lesser extent. The addition and segregation of pyrite has diluted the Ni tenor, with no evidence to suggest chemical mobilization of Ni.
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