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1.
Cu-rich massive sulfide deposits associated with mafic–ultramafic rocks in the southern portion of the Main Urals Fault (MUF) are characterized by variable enrichments in Ni (up to 0.45 wt.%), Co (up to 10 wt.%) and Au (up to 16 ppm in individual hand-specimens). The Cu (Ni–Co)-rich composition of MUF deposits, as opposed to the Cu (Zn)-rich composition of more eastward massive sulfide deposits of broadly similar age along the western flank of the Magnitogorsk arc, reflects the abundance of seafloor-exposed, Ni–Co-rich ultramafic rocks in the most external portion of the Early-Devonian Magnitogorsk forearc. Morphological, textural, and compositional differences between individual deposits are interpreted to be the result of the sulfide deposition style and, in part, of the original subseafloor lithology. One deposit produced by dominantly on-seafloor hydrothermal processes is characterized by pyrite–marcasite ≫ pyrrhotite, not so low Zn grades (occasionally up to 2 wt.%), abundant clastic facies and periodical superficial oxidation. Deposits produced by dominantly subseafloor hydrothermal processes are characterized by pyrrhotite > pyrite, very low Zn (generally < to ≪ 0.1 wt.%), volumetrically minor clastic facies, and multi-layer deposit morphology. Very low Ni/Co ratios in the on-seafloor deposit may indicate a dominant metal contribution from a mafic rather than ultramafic source. The sulfide mineralization was associated with extensive hydrothermal alteration of the host ultramafic and mafic rocks, leading to formation of abundant talc, talc–carbonate and chlorite rocks. Occurrence of large volumes of such altered lithotypes in ophiolitic belts may be considered as a potential searching criteria for MUF-type (Cu, Co, Ni)-deposits. In spite of the contrasting geodynamic environment, geological, geochemical, textural and mineralogical peculiarities of the MUF deposits in many respects are similar to those of ultramafic-hosted massive sulfide deposits along the Mid-Atlantic Ridge. In geological time, supra subduction-zone settings appear to have been more effective than mid-ocean ridge settings for preservation of ultramafic-hosted massive sulfide deposits. 相似文献
2.
The recently discovered Longtougang skarn and hydrothermal vein Cu–Zn deposit is located in the North Wuyi area, southeastern China. The intrusions in the ore district comprise several small porphyritic biotite monzonite, porphyritic monzonite, and porphyritic granite plutons and dikes. The mineralization is zoned from a lower zone of Cu-rich veins and Cu–Zn skarns to an upper zone of banded Zn–Pb mineralization in massive epidote altered rocks. The deposit is associated with skarn, potassic, epidote, greisen, siliceous, and carbonate alteration. Molybdenite from the Cu-rich veins yielded a Re–Os isochron age of 153.6 ± 3.9 Ma, which is consistent with U–Pb zircon ages of 154.0 ± 1.3 Ma for porphyritic monzonite, 154.0 ± 0.8 Ma for porphyritic biotite monzonite, and 152.0 ± 0.8 Ma for porphyritic granite. Geological observations suggest that the Cu mineralization is genetically related to the porphyritic biotite monzonite and porphyritic monzonite. All the zircons from intrusive rocks in the ore district are characterized by εHf(t) values between − 13.41 and − 4.38 and Hf model ages (TDM2) between 2054 and 1482 Ma, reflecting magmas derived mainly from a Proterozoic crustal source. Molybdenite grains from the deposit have Re values of 14.6–27.7 ppm, indicative of a mixed mantle–crust source. The porphyry–skarn abundant Cu and hydrothermal vein type Pb–Zn–Ag deposits in the North Wuyi area are related to the Late Jurassic porphyritic granites and Early Cretaceous volcanism, respectively. The Late Jurassic mineralization-related granites were derived from the crustal anatexis with some mantle input, which was triggered by asthenospheric upwelling induced by slab tearing during oblique subduction of the paleo-Pacific plate beneath the South China block, and the Early Cretaceous mineralization-related granitoids mainly from crust material formed within a series of NNE-trending basins during margin-parallel movement of the plate. 相似文献
3.
4.
The Archaean Yilgarn Craton (Western Australia) is a world-class metallogenic province, hosting considerable resources of Au, Ag, Ni, Cu, Zn and Fe. Here we present trace element compositions of pyrite from > 30 orogenic Au and 5 volcanic hosted massive sulphide (VHMS) deposits across the Yilgarn. Pyrites from VHMS deposits tend to have higher Sn, Se, Cu, Pb, Bi and lower Ni relative to orogenic deposits. VHMS deposit pyrites commonly have Co > Ni, As > 100Au, Te > Au, Se > Te. Orogenic gold deposits could be subdivided based on association of Au with As or Te. Pyrites from AuAs ores generally have Pb/Bi > 5, Se/Te > 5, Pb/Sb < 5 and Tl/Te > 100 and the majority of Au is refractory (in pyrite structure). At the same time AuTe association pyrites are characterised by lower values of Pb/Bi, Se/Te and Tl/Te, higher values of Ag/Au, Pb/Sb and Au generally resides in inclusions of different compositions. Our data can be used at the exploration stage to distinguish between VHMS vs Orogenic Au signatures. For all studied deposits inclusion populations are summarised with implications for Au and Ag deportment. Orogenic Au deposits from the Yilgarn mostly have multistage formation histories reflected in the presence of multiple generations of pyrites. However, only some deposits record multiple high Au mineralisation events. 相似文献
5.
The Hongtoushan volcanogenic massive sulfide (VMS) deposit is the largest Archean Cu–Zn deposit in China, located in the Qingyuan greenstone belt on the northern margin of the North China Craton. The Cu–Zn mineralization was stratigraphically controlled by the interbeds (~ 100 m in thickness) of mafic–felsic volcanic sets and overlain by banded iron layers. However, the relationship between VMS deposits and associated volcanics has not been examined. This study ultimately clarifies the times and sources of the volcanics and mineralization. Based on in situ zircon U–Pb and O isotope on VMS-hosting mafic, felsic volcanic rocks, banded and massive sulfide ores and postmineralization pegmatite vein, we considered that there were two main formation stages for the Qingyuan Cu–Zn deposits; one was exhalative-hydrothermal sedimentation and another was further Cu–Zn enriched by later hydrothermal processes. The timing of the first stage occurred at 2571 ± 6 Ma based on the magmatic zircons in the VMS-hosting mafic volcanic rocks, from which the inherited zircons also indicate the existence of 2.65–3.12 Ga ancient supercrustal rocks in the Qingyuan district. A modern mantle-like δ18Ozircon value of 5.5 ± 0.1‰ (2SD) for this volcanism was well preserved in the inherited core domains of ore samples. It suggests that the mafic volcanics was most likely sourced from partial melting of juvenile crust, e.g., TTG granites. A large-scale metamorphic or hydrothermal event is documented by the recrystallized zircons in sulfide ores. The timing is tightly constrained by the hydrothermal zircon U–Pb ages. They are 2508 ± 4 Ma for the banded ore, 2507 ± 4 Ma for the massive ore and 2508 ± 2 Ma for the postmineralization pegmatite vein. These indistinguishable ages indicate that the 2507 Ma hydrothermal systems played a significant role in the upgrading of the VMS Cu–Zn orebodies. The weighted δ18O values of hydrothermal zircons show a successively increasing trend from 6.0 ± 0.1‰ (2σ) for the banded ore, 6.6 ± 0.2‰ (2σ) for the massive ore to 7.3 ± 0.2‰ (2σ) for the later pegmatite vein. This variation might be induced by gradual inputting of the δ18O-rich oceanic crust and/or oceanic sediment during the hydrothermal cycling system. Considering its modern mantle-like oxygen isotope composition of 2571 Ma volcanism, a submarine volcanic hydrothermal system involving mantle plumes is a preferred setting for the Neoarchean VMS Cu–Zn deposits in the Qingyuan greenstone belt. 相似文献
6.
Vein-type gold deposits in the Atud area are related to the metagabbro–diorite complex that occurred in Gabal Atud in the Central Eastern Desert of Egypt. This gold mineralization is located within quartz veins and intense hydrothermal alteration haloes along the NW–SE brittle–ductile shear zone, as well as along the contacts between them. By using the mass balance calculations, this work is to determine the mass/volume gains and losses of the chemical components during the hydrothermal alteration processes in the studied deposits. In addition, we report new data on the mineral chemistry of the alteration minerals to define the condition of the gold deposition and the mineralizing fluid based on the convenient geothermometers. Two generations of quartz veins include the mineralized grayish-to-white old vein (trending NW–SE), and the younger, non-mineralized milky white vein (trending NE–SW). The ore minerals associated with gold are essentially arsenopyrite and pyrite, with chalcopyrite, sphalerite, enargite, and goethite forming during three phases of mineralization; first, second (main ore), and third (supergene) phases. Three main hydrothermal alteration zones of mineral assemblages were identified (zones 1–3), placed around mineralized and non-mineralized quartz veins in the underground levels. The concentrations of Au, Ag, and Cu are different from zone to zone having 25–790 ppb, 0.7–69.6 ppm, and 6–93.8 ppm; 48.6–176.1 ppb, 0.9–12.3 ppm, and 39.6–118.2 ppm; and 53.9–155.4 ppb, 0.7–3.4 ppm, and 0.2–79 ppm for zones 1, 2, and 3, respectively.The mass balance calculations and isocon diagrams (calculated using the GEOISO-Windows program) revealed the gold to be highly associated with the main mineralized zone as well as sericitization/kaolinitization and muscovitization in zone 1 more than in zones 2 and 3. The sericite had a higher muscovite component in all analyzed flakes (average XMs = 0.89), with 0.10%–0.55% phengite content in wall rocks and 0.13%–0.29% phengite content in mineralized quartz veins. Wall rocks had higher calcite (CaCO3) contents and lower MgCO3 and FeCO3 contents than the quartz veins. The chlorite flakes in the altered wall rocks were composed of pycnochlorite and ripidolite, with estimated formation temperatures of 289–295 °C and 301–312 °C, respectively. Albite has higher albite content (95.08%–99.20%) which occurs with chlorite in zone 3. 相似文献
7.
Formation of the Urals Volcanic-Hosted Massive Sulphide (VHMS) deposits is considered to be related with the intra-oceanic stage of the island arc(s) development in Late Ordovician – Middle Devonian time (ca. 460–385 Ma) based on the biostratigraphic record of ore-hosting sedimentary rocks. However, the known radiometric ages of ore hosting volcanics are very limited. Here we present direct dating results of sulphide mineralisation from the Yaman-Kasy and Kul-Yurt-Tau VHMS deposits using Re-Os isotope systematics showing similar mineralisation ages of 362 ± 9 Ma and 363 ± 1 Ma. These ages coincide with the previous Re-Os dating of the Alexandrinskoe (355 ± 15 Ma) and Dergamysh (366 ± 2 Ma) VHMS deposits. This Late Devonian (Famennian) age corresponds to the late stage of the ‘Magnitogorsk arc – Laurussia continent’ collision event and coincides with a beginning of large scale subduction-related granitoid magmatism. The younger mineralisation age relative to the biostratigraphic ages of host rocks is interpreted as one of the latest episodes of the multi-stage history of VHMS deposits development. Ar-Ar ages of sericites from metasomatic rocks of Barsuchi Log and Babaryk deposits show even younger ages clustering around 345 Ma, and testify another late hydrothermal event in the history of the Urals VHMS deposits. 相似文献
8.
The Tianhu Fe deposit (> 104 Mt at 42% TFe) in the Eastern Tianshan (NW China) is hosted in the schist, quartzite, marble, and amphibolite of the Neoproterozoic Tianhu Group. The deposit consists of disseminated, banded and massive ores. Metallic minerals are dominantly magnetite and pyrite, with minor titanite, pyrrhotite, chalcopyrite, and sphalerite. Gangue minerals include dolomite with minor forsterite, diopside, apatite, biotite, chlorite, tourmaline, tremolite, talc, calcite, and magnesite. Pyrite separates from ores have 10.7 to 54.7 ppb Re and 0.033 to 0.175 ppb common Os. Those from the massive ores have a model 1 isochron age of 535 ± 36 Ma (2σ), in agreement with the isochron age (528 ± 18 Ma) of pyrite from the banded ores by regression of seven Re–Os analyses. The Re–Os age of ~ 530 Ma reflects the timing of a hydrothermal event that remobilized the Tianhu deposit. Magnetite has Mg, Al, Ti, V, Mn, Zn, and Ga contents ranging from ~ 5 to 3500 ppm and Cr, Co, Ni, and Sn contents ranging from ~ 1 to 200 ppm. Most magnetite grains have Ca + Al + Mn and Ti + V contents similar to those of the banded iron formation (BIF). Some grains have elevated Ti and V contents, indicating that that magnetite was formed by sedimentary process and overprinted by hydrothermal activity. Pyrite has δ34SCDT values from − 9.23 to 10.96‰, indicating that the sulfur was reduced from the marine sulfates either by bacterial or thermochemical processes. Pyrite has relatively high Co (~ 346 to 3274 ppm) but low Ni (~ 5.6 to 35.4 ppm) with Co/Ni ratios ranging from ~ 10 to 270, indicating remobilization from a volcanic–hydrothermal fluid. Therefore, the Tianhu Fe deposit was originally a sedimentary type deposit but was overprinted by a hydrothermal event related to volcanic activity. 相似文献
9.
《Chemie der Erde / Geochemistry》2014,74(4):557-570
The Matomb region constitutes an important deposit of detrital rutile. The rutile grains are essentially coarse (> 3 mm), tabular and elongated, due to the short sorting of highly weathered detritus. This study reports the major, trace, and rare-earth element distribution in the bulk and rutile concentrated fractions. The bulk sediments contain minor TiO2 concentrations (1–2 wt%), high SiO2 contents (∼77–95 wt%) and variable contents in Al2O3, Fe2O3, Zr, Y, Ba, Nb, Cr, V, and Zn. The total REE content is low to moderate (86–372 ppm) marked by high LREE-enrichment (LREE/HREE ∼5–25.72) and negative Eu anomalies (Eu/Eu* ∼0.51–0.69). The chemical index of alteration (CIA) shows that the source rocks are highly weathered, characteristic of humid tropical zone with the development of ferrallitic soils. In the concentrated fractions, TiO2 abundances exceed 94 wt%. Trace elements with high contents include V, Nb, Cr, Sn, and W. These data associated with several binary diagrams show that rutile is the main carrier of Ti, V, Nb, Cr, Sn, and W in the alluvia. The REE content is very low (1–9 ppm) in spite of the LREE-abundance (LREE/HREE ∼4–40). The rutile concentrated fractions exhibit anomalies in Ce (Ce/Ce* ∼0.58 to 0.83; ∼1.41–2.50) and Eu (Eu/Eu* ∼0.42; 1.20–1.64). The high (La/Sm)N, (La/Yb)N and (Gd/Yb)N ratios indicate high REE fractionation. 相似文献
10.
The Bianjiadayuan Pb–Zn–Ag deposit in the Southern Great Xing'an Range consists of quartz-sulfide vein-type and breccia-type mineralization related to granite. Vein orebodies are localized in NW-trending extensional faults. Hydrothermal alteration is well developed and includes silicification, potassic alteration, chloritization and sericitization. Three stages of mineralization are recognized based on field evidence and petrographic observation and are marked by assemblages of quartz–arsenopyrite–pyrite (stage I), quartz–pyrrhotite–chalcopyrite–sphalerite (stage II) and quartz–galena–silver minerals (stage III). The granite, with a zircon age of 143.2 ± 1.5 Ma (n = 14, MSWD = 0.93), is subalkaline, peraluminous and is classified as A2-type granite originating in a post-orogenic extensional setting during the opening of suture zone between the North China Craton and the Siberia Craton from the Late Jurassic to the Early Cretaceous. The δ34SCDT values of sulfides, ranging from 3.19 to 10.65‰, are not consistent with the majority of magmatic hydrothermal deposits in the SGXR, possibly implying accessory source in addition to magmatic source. Microthermometric measurements show that ore minerals were deposited at intermediate temperatures (347.8–136.4 °C) with moderate salinities (2.9–14.4 wt.% NaCl). Ore-forming fluids were derived largely from magmatic hydrothermal processes, with the addition of meteoric water in late stage. Successive precipitation of Pb, Zn and Ag occurred with changes of physicochemical conditions. Overall considering mineralization features, ore-forming fluids and materials and tectonic setting and comparing with adjacent deposits, the Bianjiadayuan deposit is a mesothermal magmatic hydrothermal vein-type Pb–Zn–Ag deposit controlled by fractures and related to A2-type granite in response to the tectonic/magmatic/hydrothermal activity in late Jurassic. Besides, the explosive breccias in the west area require more attention in future exploration. 相似文献
11.
《Chemie der Erde / Geochemistry》2017,77(1):81-93
The fresh and weathered garnet amphibolites, from the Akom II area in the Archaean Congo Craton, were investigated to determine the S, Cu, Ni, Cr, and Au-PGE values. The garnet amphibolites are composed of amphibole, plagioclase, garnet, quartz, and accessory apatite, spinel, sericite, pyrite, chalcopyrite and non-identified opaque minerals. The presence of apatite, sericite, and two generations of opaque minerals suggests that they might be affected by hydrothermal alteration. They are characterized by moderate Al2O3, Fe2O3, CaO, V, Zn, and Co contents with negative Eu- and Ce-anomalies. The sulfur concentrations are variable (380–1710 ppm). According to the sulfur contents, amphibolites can be grouped into two: amphibolites with low contents, ranging between 380 and 520 ppm (av. = 457 ppm); and amphibolites with elevated contents, varying from 1140 to 1710 ppm (av. = 1370 ppm). Amphibolites contain contrast amounts of Cu (∼ 1800 to 5350 ppm) while nickel contents attain 121 ppm. Chromium contents vary from 43 to 194 ppm. Sulfur correlates positively with Cu and Cr, but negatively with Ni and Ni/Cr ratio. The total Au-PGE contents attain 59 ppb.The presence of amphibole and feldspars confirms the low degree of amphibolite weathering. The secondary minerals are constituted of kaolinite, gibbsite, goethite and hematite. Despite the accumulation of some elements, the major and trace element distribution is quite similar to that of fresh amphibolites. Nevertheless, the weathering processes lead to the depletion of several elements such as S (239–902 ppm), Cu (520–2082 ppm), and Ni (20–114 ppm). Chromium and Au-PGE show an opposite trend marked by a slight enrichment in the weathered amphibolites. Amidst the Au-PGE, Pd (60 ppb) and Pt (23 ppb) have elevated contents in the fresh rocks as well as in the weathered materials. The PPGE contents are much higher than IPGE contents in both types of materials. The Pd/Pt, Pd/Rh, Pd/Ru, Pd/Ir, Pd/Os, and Pd/Au values indicate that Pt, Rh, Ru, Ir, Os and Au are more mobile than Pd. Chondrite-normalized base metal patterns confirm the abundance of Pd and the slight enrichment of Au-PGE in weathered rocks. Palladium, Rh and Ir are positively correlated with S. Conversely Pt and Ru are negatively correlated with S and Au is not correlated with S. Despite the high and variable S and Cu contents, the garnet amphibolites possess low Au-PGE and other base metals contents. 相似文献
12.
Modern massive sulfide deposits are known to occur in diverse tectonic settings and it is generally expected that hydrothermal deposits of similar geological settings shall have more or less similar mineralogical and geochemical signatures. However, the Mount Jourdanne sulfide deposits along the super-slow spreading Southwest Indian Ridge deviate from this common concept. These sulfide precipitates are Zn-rich (up to 35 wt.%) and are characterized by high concentrations of Pb (≤ 3.5 wt.%), As (≤ 1.1 wt.%), Ag (≤ 0.12 wt.%), Au (≤ 11 ppm), Sb (≤ 967 ppm), and Cd (≤ 0.2 wt.%) which are unusual for a modern sediment-free mid-oceanic ridge system. Therefore, we have reinvestigated the sulfide samples collected during the INDOYO cruise in 1998, in order to explain their unusual mineralogy and geochemical composition. The sulfide samples are polymetallic and are classified as: a) chimneys, b) mounds, and c) hydrothermal breccias. The chimneys are small tube-like symmetrical bodies (30–40 cm high; ~ 10 cm diameter) and consist mainly of sphalerite and less chalcopyrite, set in a matrix of late amorphous silica. The inner wall shows a late-stage colloform sphalerite containing co-precipitates of galena and/or Pb–As sulfosalts. In contrast, the mound samples are dominated either by Fe-sulfides (pyrite) or by a mixture of pyrite and chalcopyrite with less sphalerite, pyrrhotite, amorphous silica and barite. Both, the chimney and mound samples, are characterized by layering and mineral zonation. The hydrothermal breccias are highly altered and mineralogically heterogeneous. They consist of silicified basaltic material that are impregnated with sulfides and contain cm-sized chimney fragments within a matrix of low-temperature minerals such as sphalerite and pyrite. The latter fragments mainly consist of chalcopyrite with isocubanite lamellae. In addition, these breccias contain late-stage realgar, boulangerite, galena, Pb–As sulfosalts and barite that are mostly confined to vugs or fractures. At least five mineralogical associations are distinguished that indicate different thermal episodes ranging from black smoker mineralization conditions to cessation of the hydrothermal activity. Based on the mineralogical associations and established literature in this regard, it is inferred that the mineralization at Mt. Jourdanne occurred mainly in three temperature domains. Above 300 °C, the chalcopyrite (with isocubanite)–pyrrhotite association formed whereas the sphalerite dominated assemblage with much less chalcopyrite and pyrite formed around and below 300 °C. The late-stage mineralization (below 200 °C) contains colloform sphalerite, galena, Pb–As sulfosalts, realgar and barite. The unusual mineralogy and trace element chemistry for this modern VHMS deposit could be explained assuming hydrothermal leaching of some felsic differentiates underneath the basaltic cover and subsequent zone refining processes. 相似文献
13.
The Arroyo Rojo deposit, located in Tierra del Fuego, is the most important polymetallic, volcanic-hosted massive sulphide in the rhyolitic belt of the Fuegian Andes. The best intercepts in drill holes indicate a true thickness of 18.6 m and concentrations of 2.2% Cu, 3.9% Pb, 14.5% Zn, 140 g/t Ag, 1.1 g/t Au). This deposit, located near the town of Ushuaia, is hosted in a Middle Jurassic volcanic and volcanoclastic sequence. Massive and semimassive bodies display stacked lenticular morphologies with disseminated mineralization in both the footwall and hanging wall. The associated hydrothermal alteration system is partially conformable with the layering of the volcanic rocks. The ores and host rocks display a penetrative tectonic foliation and were metamorphosed to greenschist facies.Previous studies have not resulted in a consensus regarding the nature and the source of ore-forming fluids and the style of deposition of the sulphides at Arroyo Rojo. In this study, both stable and radiogenic isotopes were used develop a better understanding of these aspects of the deposit.Hydrogen and oxygen isotopes indicate that an evolved seawater mixed with significant contributions from other fluid reservoirs such as magmatic and/or metamorphic waters was the most likely source of the ore-forming fluids. These fluids underwent significant interaction with the underlying volcanic and sedimentary rocks, which promoted partial (Sr isotopes) or full (Pb isotopes) homogenization of radiogenic isotopes. δ34SCDT values suggest that the sulphur was derived from several sources: biogenic reduction of seawater sulphate (BSR) in a restricted to closed basin was mixed with a heavier component derived from inorganic reduction of seawater sulphate (TRS) and possibly from sulphur leached from igneous footwall rocks and/or direct contribution from magmatic fluids.Lateral infiltration of hydrothermal fluids resulted in the formation of a halo of semimassive to disseminated ore due to the replacement of porous, reactive glassy and breccia tuffs.As a result of the hydrothermal circulation, two styles of mineralization are observed in the Arroyo Rojo deposit: a stringer zone and a halo of semimassive to disseminated ore corresponding to sub-seafloor replacement, and syn-sedimentary mineralization consisting of massive sulphides.This model is consistent with the geodynamic context of the study area: a narrow, deep-marine volcano-tectonic rift parallel to the Andean side of South America and related to the initial break-up of Gondwana (ca. 145 Ma). 相似文献
14.
The Ranger 1 unconformity-related uranium deposit in the Northern Territory of Australia is one of the world's largest uranium deposits and has ranked in the top two Australian producers of uranium in recent years. Mineralisation at the Ranger, Jabiluka and other major unconformity-related deposits in the Alligator Rivers Uranium Field (ARUF) occurs in Paleoproterozoic metamorphic basement rocks immediately beneath the unconformity with the Paleo- to Mesoproterozoic McArthur Basin.The sites of uranium mineralisation and associated alteration at the Ranger 1 deposit (Number 3 orebody) were fundamentally controlled by reactivated shear zones that were initiated during the regional Nimbuwah tectonothermal event. The timing of shearing at medium metamorphic grade was constrained by ion microprobe U–Pb dating of zircons in two pegmatites, one weakly foliated (1867.0 ± 3.5 Ma) and another that is unfoliated and cuts the shear fabric (1862.8 ± 3.4 Ma). The younger age of ~ 1863 Ma represents the minimum age of D1 shearing during the Nimbuwah event at the Ranger 1 deposit (Number 3 orebody). Titanite within veins of amphibole-plagioclase-apatite yielded an ion microprobe U–Pb age of 1845.4 ± 4.2 Ma, which represents a previously unrecognised hydrothermal event in the ARUF. Based on previous data, retrograde hydrothermal alteration during D2 reactivation of D1 shear zones is interpreted to have occurred at ~ 1800 Ma during the regional Shoobridge tectonothermal event.Detailed paragenetic observations supported by whole-rock geochemical data from the Ranger 1 deposit (Number 3 orebody) reveal a sequence of post-D2 hydrothermal events, as follows. (1) Intense magnesium-rich chlorite alteration and brecciation, focussed within schists of the Upper Mine Sequence in the Cahill Formation. (2) Silicification of Lower Mine Sequence carbonate rock units and overlying schist units, comprising quartz ± Mg-foitite (tourmaline) ± muscovite ± pyrite ± marcasite, and rare uraninite (early U1). (3) Formation of main stage uranium ore and heterolithic breccias including clasts of olivine–phyric dolerite, with breccia matrix composed of uraninite (U1), Mg-chlorite ± Mg-foitite and minor pyrite and chalcopyrite. (4) A second generation of uraninite (U2) veinlets with disordered graphitic carbon and quartz of hydrothermal origin. (5) Late-stage veinlets of massive uraninite (U3). As inferred in a previous study and confirmed herein, olivine–phyric dolerite dykes at Ranger are mineralised and chloritised, and are geochemically similar to the regional Oenpelli Dolerite. A maximum age for uranium mineralisation at the Ranger 1 deposit is therefore set by the age of the Oenpelli Dolerite (~ 1723 Ma).In-situ ion microprobe U–Pb analysis of texturally oldest U1 uraninite yielded a discordia array with a 206Pb/238U-207Pb/235U upper intercept age of 1688 ± 46 Ma. The oldest individual ion microprobe 207Pb–206Pb age is 1684 ± 7 Ma whereas the oldest age determined by in-situ electron microprobe chemical dating of U1 uraninite is ~ 1646 Ma. Another sample containing both U1 and U2 uraninite yielded discordant data with a 206Pb/238U–207Pb/235U upper intercept age of 1421 ± 68 Ma. When the 207Pb/206Pb ages are considered the data are suggestive of U2 uraninite formation and possible resetting of the U1 age between ~ 1420 Ma and ~ 1040 Ma. All ion microprobe analyses of U1 and U2 uraninite indicate variable and possibly repeated lead loss. In contrast ion microprobe U–Pb dating of the third generation of uraninite (U3) yielded several near-concordant analyses and a 206Pb/238U–207Pb/235U upper intercept age of 474 ± 6 Ma. This age is supported by electron microprobe chemical ages of U3 uraninite between 515 Ma and 385 Ma.The new results constrain the timing of initial uranium mineralisation at the Ranger 1 deposit (Number 3 orebody) to the period ~ 1720 Ma to ~ 1680 Ma, which just overlaps with a previous U–Pb age of 1737 ± 20 Ma for uraninite-rich whole-rock samples. Our results are consistent with individual laser-ICPMS 207Pb/206Pb and chemical ages of uraninite as old as 1690–1680 Ma reported from other deposits and prospects in the ARUF.Whole-rock geochemical data in this study of the Ranger 1 deposit (Number 3 orebody) and in other studies in the ARUF demonstrate that zones of intense chloritisation associated with uranium mineralisation experienced large metasomatic gains of Mg, U, Co, Ni, Cu and S and losses of Si, Na, Ca, Sr, Ba, K, Rb, Y and the light REE. More broadly in the ARUF, a regionally extensive illite–hematite ± kaolinite-bearing ‘paleoregolith’ zone in basement beneath the McArthur Basin exhibits depletion of about half of its uranium as well as major losses in Na, Sr, Pb, Ba and minor losses of Mg. These features together with new petrographic observations suggest this zone is a regional sub-McArthur Basin alteration zone produced by interaction with diagenetic or hydrothermal fluids of primary basinal origin, rather than representing a low-temperature paleo-weathering zone before the deposition of the McArthur Basin, as previously suggested.Based on these results and a synthesis of previous work, a new multi-stage model is proposed for the Ranger 1 ore-forming mineral system that may apply to other major unconformity-related uranium deposits in the ARUF and which may be used for targeting new deposits in the region. As in most recent models, oxidised diagenetic brines within the McArthur Basin are envisaged as crucial in mobilising uranium. However, a different architecture of fluid flow is proposed involving the sub-unconformity regional basement alteration zone as a preferential source of leached uranium. Possibly driven by convection during regional magmatism at ~ 1725–1705 Ma, oxidised basinal brines were drawn downwards and laterally through fault networks and fractures in the regional sub-unconformity alteration zone, leaching uranium from hematite-altered basement rocks. Simultaneously within deeper and lateral parts of the hydrothermal system, Mg-metasomatism produced chloritic alteration and brines with increased acidity and silica content (from the desilicification of the basement rock), analogous to processes described in sub-seafloor hydrothermal systems. Silicification occurred locally (e.g., Ranger deposit) within upflow zones of convective systems due to decreases in temperature and/or pressure of the brines and/or CO2 generation during carbonate dissolution. Interruptions to convection during transient regional extensional or strike-slip tectonic events resulted in generalised lateral and downwards flow of fluids from the McArthur Basin through deepened zones of sub-unconformity alteration, transferring leached uranium into reactivated shear zones within the basement. The main stage of uraninite precipitation at the Ranger deposit and elsewhere in the ARUF is proposed to have occurred between ~ 1720 Ma and ~ 1680 Ma as a result of reduction of oxidised and evolved basin-derived ore fluids during reaction with pre-existing Fe2 +-bearing minerals and/or mixing of the ore fluids with basement-reacted silica-rich brines.A second, volumetrically minor but locally high-grade, stage of uraninite mineralisation was associated with hydrothermal disordered carbon and quartz of presently unknown origin. Available data suggest formation between ~ 1420 Ma and ~ 1040 Ma. Almost a billion years later at ~ 475 Ma, fluids capable of mobilising uranium again resulted in uraninite (U3) deposition as sparse veinlets in the Ranger deposit, representing the first documentation of uranium mineralisation of this age in the region. 相似文献
15.
Variable intensity of hydrothermal alteration of the Veia Alta basalt flow, Ametista do Sul, Brazil, exerted the fundamental control on the shape and size of the amethyst geodes. The loss on ignition (LOI) of the host basalt is used as a proxy for intensity of alteration and has direct relationship with the height of the geodes (up to 150 cm in the three study mines) and with the prolaticity of geodes. All rocks with LOI > 5 wt.% host prolate geodes and all oblate geodes are hosted in rocks with LOI < 5 wt.%. An additional observation is the extensive mobility of several elements during hydrothermal alteration (variable LOI), including SiO2, K2O and Rb. The hydrothermal origin of the geodic cavities is thus established and their shapes explained by the empirical observation of the results from a previous numerical simulation experiment. 相似文献
16.
In-situ laser ablation ICP-MS analyses on iron oxides in itabirite and iron ore from the Quadrilátero Ferrífero (Brazil) reveal a wide range in trace element abundances (e.g., average concentrations in hematite: Al = 40–2200 ppm, Mg = 1–930 ppm, Mn = 5–540 ppm, Ti = 3–500 ppm, V = 2–390 ppm, Cr = 1–98 ppm, As = 0.5–60 ppm). The chemistry of early hematite stages is mostly inherited from host rock and precursor magnetite, e.g., Mn concentrations correlate with bulk Mn content in itabirite. With progressive iron ore formation and modification, external fluids play a more prominent role. This is reflected by REE-Y switching from seawater-like Y/Ho ratios (> 44) in early-, to more chondrite-like Y/Ho ratios (< 34), in late-hematite stages, likely due to fluid–rock reactions with country rocks (e.g., phyllites) or exchange with magmatic hydrothermal fluids.The following ore formation stages and key processes, supported by mineral scale mass balance calculations, are constrained: (1) martitisation, cogenetic with gangue leaching, is driven by large volumes of oxidising, Si-undersaturated fluids resulting in an absolute depletion of Mg, Mn, Al, Ti, Ni and Zn, and enrichment of Pb, As, LREE and Y; (2) the formation of granoblastic hematite and locally microplaty hematite represents a largely isochemical recrystallisation of magnetite and/or martite accompanied by a depletion of Mg and Y and an elevated Ti mobility at the mineral scale; and (3) precipitation of schistose and vein-hosted specular hematite along shear and fracture zones is driven by an external Fe–Si-rich hydrothermal fluid likely under high fluid/rock ratios. 相似文献
17.
《Chemie der Erde / Geochemistry》2016,76(4):659-676
The Hercynian late-orogenic granites from the Gerês massif, northern Portugal, underwent intense hydrothermal activity along tectonic structures striking N-S and NE-SW. The first hydrothermal stage is characterized by the albitization of feldspars (primary K-feldspar and plagioclase) followed by the dissolution of magmatic quartz, the chloritization of biotite, and the muscovitization of magmatic biotite and feldspars and occasionally of authigenic albite. Whole-rock geochemistry shows a decrease of SiO2, K2O and Rb and an increase of Na2O, Al2O3 and Sr amounts during the albitization. The second hydrothermal stage is characterized by a mineral assemblage consisting of secondary quartz, albite, chlorite, hematite, apatite, muscovite, epidote, sphene and carbonates, which infilled the cavities produced by the early quartz leaching.Mass balance calculations demonstrate a noticeable element mobilization during the granite alteration. The average ∑REE of the Gerês granite is nearly constant at 154 ppm, but ranges from 91 to 163 ppm in the altered rocks. A relative LREE depletion and a slight HREE enrichment associated with a negative Eu anomaly characterize the feldspathization process of Gerês granite. The average ∑REE of the Carris granite is at 159 ppm but in the altered epidote + chlorite + hematite assemblage it reaches about 201 ppm with a slight HREE increase.Two different fluids were involved in the hydrothermal alteration. A first aqueous fluid (Lw1), with a low to intermediate salinity (<10 wt.% eq. NaCl) circulated along the main structures (N-S, NE-SW and NW-SE), characterized by entrapment temperature lower than 350 °C and maximum pressure of 115 MPa followed by a later colder and more saline fluid (Lw2) under a temperature of 220 °C and a pressure of about 27 MPa.Oxygen isotope data obtained on magmatic quartz indicate δ18Oquartz of + 9.3 and + 11.0‰, pointing to an interaction of magmatic fluids with others of meteoric origin. For the secondary quartz, δ18Owater of +0.5 and +0.7‰ were calculated for a temperature of 250 °C, suggesting a meteoric fluid with a possible seawater signature.The K-Ar data of K-feldspar from the altered rocks confirm an age of 273.6 ± 11.7 Ma, attributed to the first alteration process. Younger K-Ar ages between 155.8 ± 6.7 Ma and 124 ± 5.3 Ma were also obtained in the feldspathized rocks, confirming the late hydrothermal activity.Albitization and quartz dissolution of granitic rocks from the Gerês massif occurred at depths shallower than 5 km, induced by the circulation of fluids along brittle structures, during the orogenic uplift and extensional tectonics which affected the Iberian Massif in the Early Permian. A second major event is attributed to late hydrothermal circulations of aqueous brines until a depth of about 3 km, presumably derived from interaction with sub-surface evaporites throughout Late Jurassic to Early Cretaceous. These late hydrothermal events probably reflect the rifting episodes and the rising of geothermal gradient, associated with the opening of the Atlantic Ocean and Gulf of Biscay, respectively. 相似文献
18.
The Doriri Creek (DC) Ni–Pd–Pt prospect was discovered in 1966 in the Papuan Ultramafic Belt (PUB) in PNG. The DC was interpreted as a hydrothermal Ni accumulation. The DC is located in the southern proximity of Mt Suckling (~ 180 km SE of Port Moresby), where local intrusive rocks are intermediate to acid dykes and small stocks, within the tec tonized contact zone of the Australian and Woodlark Plates. The active volcanoes of Mount Victory and Waiowa indicate recent thermal activity in the area.The Doriri Creek prospect is the result of episodic hydrothermal fluid flow running through the Doriri prospect, that resulted in Ni concentration of up to 1.55 wt.%, formed by alteration of an ultramafic unit of peridotites/pyroxenites within a Mg-rich gabbronorite envelope. Ni was concentrated in chlorite and serpentine group minerals in addition to Fe oxides, with a minor amount in pentlandite in locally sulfidic samples. Ore mineralogy is also associated with a high phosphorous content as apatite, that concentrates LREE (light rare earth elements). Palladium concentrations are up to 0.37 ppm. Platinum is present in concentrations up to 0.06 ppm within the ore.The alteration halo associated with Doriri Creek mineralization is ~ 100 m in width. Primary mineralogy comprises pyroxene, olivine and plagioclase, which have been altered extensively to amphibole and chlorite–serpentine group minerals. This halo is characterized by enrichments of U, K and W over background values.Local magnetite concentration is up to ~ 35% of whole rock, which is very pronounced in the sulfide rich area of the system. The top part of the DC system is overprinted by tropical weathering at metric scale, which displays LREE enrichment and positive Ce anomalies.The Papuan Ultramafic Belt is described as a highly prospective ground for hydrothermal Ni systems based on its availability of Ni, active thermal flow engines, and the geologic regional context dominated by mafic rock suites and the presence of carbonate/siliciclastic units. 相似文献
19.
Trace element geochemistry was studied in geothermal fluids in Iceland. The major and trace element compositions of hot springs, sub-boiling, and two-phase (liquid and vapor) wells from 10 geothermal areas were used to reconstruct the fluid composition in the aquifers at depth. Aquifer fluid temperatures ranged from 4 to 300 °C, pH values between 4.5 and 9.3, and fluids typically contained total dissolved solids <1000 ppm, except in geothermal areas that have seawater and seawater-meteoric water mixtures. Trace alkali elements Li, Rb and Cs are among the most mobile elements in aquifer fluids, with concentrations in the range of <1 ppb to 3.49 ppm Li, <0.01 to 57 ppb Cs, and <1 ppb to 3.77 ppm Rb. Their chemistry is thought to be dominated by rock leaching and partitioning into Na- and K-containing major alteration minerals. Arsenic, Sb, Mo and W are typically present in concentrations in the range of 1–100 ppb. They are relatively mobile, yet Mo may be limited by molybdenite solubility. The alkaline earth elements Ba and Sr are quite immobile with concentrations in the range of <0.1–10 ppb Ba and <1–100 ppb Sr in the dilute fluids, but up to 5.9 ppm Ba and 8.2 ppm Sr in saline fluids. These elements show a systematic relationship with Ca, possibly due to substitution for Ca in Ca-containing major alteration minerals like calcite, epidote and anhydrite. Incorporation into major Ca-minerals may also be important for Mn. Many metals including Fe, Cr, Ni, Zn, Cu, Co, Pb and Ag have low mobility and concentrations, typically <1 ppb for Ag, Cd, Co, Cr, Cu, Ni, and Pb, <10 ppb for Zn and < 100 ppb for Fe, although for some metals higher concentrations are associated with saline fluids. Based on the metals assessed, saturation is approached with respect to many sulfide minerals and in some cases oxide minerals but Cu, Ni and Pb minerals are slightly but systematically undersaturated, and Ag phases significantly undersaturated. Evaluation of mineral-fluid equilibria for these metals is problematic due to their low concentrations, problems associated with assessing the aqueous species distribution by thermodynamic calculations, and uncertainties concerning the exact minerals possibly involved in such reactions. Reaction path calculations, poor comparison of concentrations measured in the samples collected at the wellhead and published downhole data as well as boiling, cooling and mass precipitation calculations suggest removal of many metals due to changes upon depressurization boiling and conductive cooling of the aquifer fluids as they ascend in wells. These results imply that processes such as mass precipitation upon fluid ascent may be highly important and emphasize the importance of considering mass movement in geothermal systems. 相似文献
20.
The Yangyang iron-oxide–apatite deposit in South Korea has undergone multiple episodes of igneous activity, deformation, hydrothermal alteration, and iron-oxide–apatite (IOA) mineralization. The iron orebodies occur as concordant- to discordant-layered lenticular or massive magnetite and/or magnetite–pyrite ores. The iron mineralization occurs along a N–S-trending shear zone within the Yangyang syenite, which experienced both early ductile and later brittle deformations. Alteration was caused mainly by the injection of hydrothermal fluid through the shear zone, leading to Fe–P mineralization. We recognize multiple stages of alteration in the Yangyang deposit, based on a paragenesis that is defined by distinct mineral assemblages including Na–Ca–K alteration phases (e.g., albite, diopside, actinolite, and biotite) and accessory minerals containing high field strength elements (e.g., apatite, sphene, allanite, and monazite). The alteration around the magnetite ore body shows an evolutionary trend from Ca (–Na) alteration, through K to phyllic alterations. The Fe–P mineralization is associated with the Ca–K and K alteration products. The iron orebodies are hosted by deformed and altered syenite, which intruded the Paleoproterozoic gneiss complexes at 233 ± 1 Ma (SHRIMP U–Pb zircon age) in a post-collisional tectonic setting. LA-ICP-MS U–Pb dating of REE-rich sphene and apatite from the iron ores and alteration products yields Fe mineralization ages of 216 ± 3 Ma (sphene) and 212 ± 13 Ma (apatite). This is the first time, which IOA-type mineralization in the Korean Peninsula was dated as Triassic age related to post-collisional magmatism within the Gyeonggi Massif, South Korea. The U–Pb system was subsequently reset (208 ± 3 Ma–sphene and 151 ± 13 Ma–apatite) by Jurassic and Cretaceous magmatism. This unique geological evolution was responsible for Mesozoic metal enrichment and remobilization into suitable structural traps in the Yangyang district. 相似文献