Oxidized sulfur-rich arc magmas formed porphyry Cu deposits by 1.88 Ga.
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ABSTRACT:
SUBMITTER: Meng X
PROVIDER: S-EPMC8044198 | biostudies-literature |
REPOSITORIES: biostudies-literature
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Project description:Porphyry systems supply most copper and significant gold to our economy. Recent studies indicate that they are frequently associated with high Sr/Y magmatic rocks, but the meaning of this association remains elusive. Understanding the association between high Sr/Y magmatic rocks and porphyry-type deposits is essential to develop genetic models that can be used for exploration purposes. Here we present results on a Pleistocene volcano of Ecuador that highlight the behaviour of copper in magmas with variable (but generally high) Sr/Y values. We provide indirect evidence for Cu partitioning into a fluid phase exsolved at depths of ~15 km from high Sr/Y (>70) andesitic magmas before sulphide saturation. This lends support to the hypothesis that large amounts of Cu- and S-bearing fluids can be accumulated into and released from a long-lived high Sr/Y deep andesitic reservoir to a shallower magmatic-hydrothermal system with the potential of generating large porphyry-type deposits.
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Project description:Hydrothermal fluid is essential for transporting metals in the crust and mantle. To explore the potential of Cu isotopes as a tracer of hydrothermal-fluid activity, Cu-isotope fractionation factors between Cl-bearing aqueous fluids and silicate magmas (andesite, dacite, rhyolite dacite, rhyolite and haplogranite) were experimentally calibrated. Fluids containing 1.75-14 wt.% Cl were mixed together with rock powders in Au95Cu5 alloy capsules, which were equilibrated in cold-seal pressure vessels for 5-13 days at 800-850°C and 2 kbar. The elemental and Cu-isotopic compositions of the recovered aqueous fluid and solid phases were analyzed by (LA-) ICP-MS and multi-collector inductively coupled plasma mass spectrometry, respectively. Our experimental results show that the fluid phases are consistently enriched in heavy Cu isotope (65Cu) relative to the coexisting silicates. The Cu-isotope fractionation factor (Δ65CuFLUID-MELT) ranges from 0.08 ± 0.01‰ to 0.69 ± 0.02‰. The experimental results show that the Cu-isotopic fractionation factors between aqueous fluids and silicates strongly depend on the Cu speciation in the fluids (e.g. CuCl(H2O), CuCl2 - and CuCl3 2-) and silicate melts (CuO1/2), suggesting that the exsolved fluids may have higher δ65Cu than the residual magmas. Our results suggest the elevated δ65Cu values in Cu-enriched rocks could be produced by addition of aqueous fluids exsolved from magmas. Together with previous studies on Cu isotopes in the brine and vapor phases of porphyry deposits, our results are helpful for better understanding Cu-mineralization processes.
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Project description:Felsic magmatic systems represent the vast majority of volcanic activity that poses a threat to human life. The tempo and magnitude of these eruptions depends on the physical conditions under which magmas are retained within the crust. Recently the case has been made that volcanic reservoirs are rarely molten and only capable of eruption for durations as brief as 1,000 years following magma recharge. If the "cold storage" model is generally applicable, then geophysical detection of melt beneath volcanoes is likely a sign of imminent eruption. However, some arc volcanic centers have been active for tens of thousands of years and show evidence for the continual presence of melt. To address this seeming paradox, zircon geochronology and geochemistry from both the frozen lava and the cogenetic enclaves they host from the Soufrière Volcanic Center (SVC), a long-lived volcanic complex in the Lesser Antilles arc, were integrated to track the preeruptive thermal and chemical history of the magma reservoir. Our results show that the SVC reservoir was likely eruptible for periods of several tens of thousands of years or more with punctuated eruptions during these periods. These conclusions are consistent with results from other arc volcanic reservoirs and suggest that arc magmas are generally stored warm. Thus, the presence of intracrustal melt alone is insufficient as an indicator of imminent eruption, but instead represents the normal state of magma storage underneath dormant volcanoes.
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Project description:Porphyry-type deposits are a vital source of green technology metals such as copper and molybdenum. They typically form in subduction-related settings from large, long-lived magmatic systems. The most widely accepted model for their formation requires that mantle-derived magmas undergo an increase in volatiles and ore-forming constituents in mid- to lower crustal reservoirs over millions of years, however, this is mostly based on observations from shallow, sporadically exposed parts of porphyry systems. To examine this paradigm, we have evaluated the timeframe and geochemical signatures of magmatism in a ~ 8 km palaeodepth cross-section through plutonic and volcanic rocks of the classic Yerington magmatic system, Nevada. We show that the magmas in the upper parts of the system (< 8 km) underwent a major and rapid change in chemistry over a period of < 200 kyrs that is coincident with the initiation of ore formation. We attribute this change to a shift from extraction of quartz monzodiorite and quartz monzonite magmas evolving in mid-crustal reservoirs, and that had relatively poor ore-forming potential, to extraction of volatile-rich granitic magmas from greater (~ 30 km) depths. As the granites crystallised, late stage melts were intruded through the carapace as aplite dykes which contain traceable expressions of the porphyry deposit-forming fluids. The rapid nature of the shift in ore-forming potential narrows the temporal-geochemical footprint of magmas associated with porphyry mineralisation and provides new constraints for exploration models.
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Project description:Porphyry deposits are natural suppliers of most copper and significant gold to our society. Whereas the Cu-richest (Au-poor) porphyries are related to Andean-type subduction and typical calc-alkaline magmatism, the Au-richest porphyries are associated with high-K calc-alkaline to alkaline magmatism in late to post-subduction or post-collision and extensional settings, and subordinately with calc-alkaline magmatism. The reasons behind these associations and the large variations in metal endowments of porphyry Cu-Au deposits remain obscure. Here, I show that porphyry Cu-Au deposits define two distinct trends in Au vs. Cu tonnage plots (Cu-rich and Au-rich). Metal endowments for both trends grow larger the longer the mineralization process. However, Au is precipitated at much higher rates in Au-rich than in Cu-rich porphyry deposits. Using Monte Carlo simulations of petrologic processes, I show that whereas Cu-rich porphyries require large amounts of magma and water to be formed, Au-rich porphyries are the result of a better efficiency of Au precipitation.
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Project description:Subduction zone magmas are more oxidised on eruption than those at mid-ocean ridges. This is attributed either to oxidising components, derived from subducted lithosphere (slab) and added to the mantle wedge, or to oxidation processes occurring during magma ascent via differentiation. Here we provide direct evidence for contributions of oxidising slab agents to melts trapped in the sub-arc mantle. Measurements of sulfur (S) valence state in sub-arc mantle peridotites identify sulfate, both as crystalline anhydrite (CaSO4) and dissolved SO42- in spinel-hosted glass (formerly melt) inclusions. Copper-rich sulfide precipitates in the inclusions and increased Fe3+/?Fe in spinel record a S6+-Fe2+ redox coupling during melt percolation through the sub-arc mantle. Sulfate-rich glass inclusions exhibit high U/Th, Pb/Ce, Sr/Nd and ?34S (+?7 to +?11‰), indicating the involvement of dehydration products of serpentinised slab rocks in their parental melt sources. These observations provide a link between liberated slab components and oxidised arc magmas.
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Project description:Porphyry deposits are copper-rich orebodies formed by precipitation of metal sulphides from hydrothermal fluids released from magmatic intrusions that cooled at depth within the Earth's crust. Finding new porphyry deposits is essential because they are our largest source of copper and they also contain other strategic metals including gold and molybdenum. However, the discovery of giant porphyry deposits is hindered by a lack of understanding of the factors governing their size. Here, we use thermal modelling and statistical simulations to quantify the tempo and the chemistry of fluids released from cooling magmatic systems. We confirm that typical arc magmas produce fluids similar in composition to those that form porphyry deposits and conclude that the volume and duration of magmatic activity exert a first order control on the endowment (total mass of deposited copper) of economic porphyry copper deposits. Therefore, initial magma enrichment in copper and sulphur, although adding to the metallogenic potential, is not necessary to form a giant deposit. Our results link the respective durations of magmatic and hydrothermal activity from well-known large to supergiant deposits to their metal endowment. This novel approach can readily be implemented as an additional exploration tool that can help assess the economic potential of magmatic-hydrothermal systems.
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Project description:Elevated H2O concentrations and oxygen fugacities are two fundamental properties that distinguish magmas formed in subduction zones from new crust generated at mid ocean ridges. However, the mechanism of magma oxidation, and how it relates to the increase in H2O remains unclear. In this study, we use infrared spectroscopy of mantle wedge orthopyroxene to trace the temporal and spatial evolution of oxygen fugacity during transport of hydrous arc melts towards the crust. A positive correlation between equilibrium oxygen fugacity and orthopyroxene H2O concentrations for the peridotite samples studied allowed the assignment of specific, commonly-observed absorption bands to redox-sensitive crystallographic defects. H2O content associated with these redox-sensitive defects increases in concentration across individual crystals, uniquely preserving the time-dependent transition from reduced to oxidised conditions during the migration of hydrous melts through the mantle wedge. A separate, but related process of reaction with H2 occurring primarily during the earliest stages of melt-mantle reaction may be fundamental in generating the oxidised nature of hydrous melts. Our study proposes that the oxidised nature of arc magmas may not be a primary feature, but is instead acquired progressively as hydrous primary melts react with the surrounding mantle.
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Project description:The mechanisms of transfer of crustal material from the subducting slab to the overlying mantle wedge are still debated. Mélange rocks, formed by mixing of sediments, oceanic crust, and ultramafics along the slab-mantle interface, are predicted to ascend as diapirs from the slab-top and transfer their compositional signatures to the source region of arc magmas. However, the compositions of melts that result from the interaction of mélanges with a peridotite wedge remain unknown. Here we present experimental evidence that melting of peridotite hybridized by mélanges produces melts that carry the major and trace element abundances observed in natural arc magmas. We propose that differences in nature and relative contributions of mélanges hybridizing the mantle produce a range of primary arc magmas, from tholeiitic to calc-alkaline. Thus, assimilation of mélanges into the wedge may play a key role in transferring subduction signatures from the slab to the source of arc magmas.
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Project description:Understanding the processes leading to the broad chemical variability of arc magmas is an essential, yet not fully elucidated, issue in Earth Sciences. Here, I show that Zn-MgO-SiO2 systematics of magmatic arc rocks correlate significantly with arc thickness. Because Zn-MgO-SiO2 systematics are mostly controlled by fractionation of different mineral phases, this suggests a systematic change in the proportions of fractionating mineral assemblages depending on arc thickness. Using a mass balance model with a Monte Carlo approach, I show that Zn-MgO-SiO2 systematics can be quantitatively explained by a continuous transition from plagioclase-dominated fractionating assemblages in thin arcs to amphibole-garnet-magnetite-dominated assemblages in increasingly thicker arcs. Most likely, such a systematic change results from the increase of average depth of magma differentiation that is ultimately controlled by arc thickness. Results presented have implications on the causes of different geochemical trends in arcs, the role of arcs as H2O filters, and their association with porphyry deposits.
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