Polyphase Inclusions Research Articles

A rapid transition from subduction to Barrovian metamorphism: geochronology of mafic–ultramafic relicts of oceanic crust in the Central Alps, Switzerland

Relicts of subducted oceanic lithosphere provide key information for the tectonic reconstructions of convergent margins. In the Central Alps, such relicts occur as isolated mafic–ultramafic lenses within the migmatites of the southern Adula nappe and Cima-Lunga unit. Analysis of the major-, minor-, and accessory minerals of these ophiolitic relicts, combined with zircon and rutile U–Pb ages and zircon oxygen isotopes, allows the reconstruction of different stages of their complex evolution. The mafic–ultramafic suite in Valle di Moleno consists of chlorite-harzburgites associated with metarodingites and retrogressed eclogites. Relic omphacite and kyanite in retrogressed eclogites provide evidence for subduction-related metamorphism. Increasing XPrp in the garnet mantle towards the rim documents heating during high-pressure metamorphism up to 800–850 °C. Polyphase inclusions and chemical zoning in garnet suggest fluid-assisted melting during high-pressure metamorphism dated at 31.0 ± 0.9 Ma. In Val Cama, chlorite-harzburgites, metarodingites and calcsilicate-metasediments occur. Detrital zircon ages in the metasediment suggest a Mesozoic deposition. The metarodingite-metaperidotite-metasediment association and the low δ18O signatures of zircon (δ18O 3.0–3.7‰), inherited from seafloor metasomatism of the protoliths, show that the rocks are derived from former altered oceanic crust. Amphibolite facies metamorphism related to the Central Alps Barrovian evolution in Val Cama occurred at 28.8 ± 1.5 Ma. The combined data from Moleno and Cama indicate a rapid transition (~ 2 Ma) from subduction to collisional metamorphism with corresponding exhumation rates of 3–6 cm/year. Fast exhumation tectonics may have been favored by slab break-off or slab extraction. U–Pb dating of rutile from both localities yields ages of ~ 20 Ma, suggesting that these rocks remained at amphibolite-facies conditions for about 10 Ma and underwent a second fast exhumation of 3 cm/year associated with vertical movements along the Insubric line.

Carbon-rich polyphasic inclusions in postcollisional mafic magmatic rocks from the Dabie Shan, China: Implications for the carbon cycle in continental subduction zones

Subduction is a fundamental geodynamic process that transfers carbon from Earth’s surface into the mantle. However, current understanding of the migration mechanisms, final storage region, and species involved in carbon recycling from continental crust remains limited. Here, we investigated the compositions of polyphasic inclusions and Mg isotopes in postcollisional mafic magmatic rocks from the Dabie Shan region of China. The main rock-forming minerals contained two distinct types of polyphasic inclusions, which displayed systematic differences in daughter mineral/gaseous phase assemblages, including host-like silicates ± carbonates (magnesite, dolomite, and calcite) + CH4 and carbonates + talc ± SiO2 (aqueous) + CH4, respectively. These inclusions indicate that carbon-rich silicate melts and carbon-rich magmatic fluids were trapped by host minerals during magmatic processes. The abundant carbonates and CH4 in both types of inclusions suggest that the mantle source of these postcollisional mafic magmatic rocks was rich in carbon, most likely existing in the forms of CO2 and CH4. Moreover, the studied postcollisional mafic magmatic rocks have mantle-like Mg isotope compositions, with δ26Mg values ranging from −0.23‰ to −0.16‰. The combined observations of polyphase inclusions and Mg isotopes indicate that a substantial carbon-rich mantle domain arose from the metasomatism of silicate melts derived from subducted continental slabs that had dissolved a certain quantity of CO2 and CH4. We proposed that continental subduction is an efficient pathway for transporting crustal carbon into an orogenic subcontinental lithospheric mantle wedge, where the recycled carbon can be stored for >100 m.y. and eventually released to the surface during postcollisional magmatism.

Mineral assemblages from chromitites of the Alapaevsk dunite-harzburgite massif (Middle Urals)

Research subject. Minerals and mineral assemblages of noble elements in chromitites of the Alapaevsk massif. Aim. A systematic mineralogical study of high-chromium (Cr) and alumina-rich (Al) chromitites with the development of a sequence scheme for mineral formation, including platinum-group minerals (PGMs) and gold alloys. Materials and Methods. Samples of high-Cr and Al chromitites from chromite deposits in various parts of the Alapaevsk massif. Scanning electron microscopy (Tescan VEGAII XMU and JSM-6390LV Jeol with EDX INCA Energy 450 X-Max 80 spectrometers) and electron microprobe analysis (Cameca SX 100 with five wave spectrometers) were used. Results. A diagram showing the sequence of mineral formation in chromitites was designed; primary and secondary mineral assemblages were distinguished, with the latter assemblage being divided into early and late mineral associations. Primary assemblages of high-Cr (Cr2O3 > 50 wt %) and Al (Cr2O3 < 50 wt %) ores are represented by similar minerals, including chromespinel, clinopyroxene, and olivine, with characteristically distinct compositions of these minerals in each type of ores. Minerals of the primary assemblage are synchronous with chrome-spinel and are represented by pentlandite, Cu-bearing pentlandite, chalcopyrite, pyrrhotite, bornite, as well as PGMs (laurite RuS2, erlichmanite OsS2, native osmium) and Cu-rich gold. Minerals of the secondary early association occur in the form of polyphase inclusions within chrome-spinel. Polyphase inclusions are composed of Cr-bearing chlorite, amphibole, garnet, sulfides (millerite, heazlewoodite) and minerals of native elements, including (Ni, Cr)-bearing copper, nickel-bearing copper, (Cu, Fe, Cr)-bearing nickel, awaruite. Noble metal minerals from the secondary early association were found only in Al chromitites and are represented by laurite, Pt- and Pd arsenides and stibnides, Ru-bearing pentlandite, and high-grade native gold. The secondary late mineral association consists of native copper and awaruite, which are intergrown with serpentine in high-Cr ore. The temperature conditions for the formation of secondary assemblages were estimated using a chlorite geothermometer. The formation temperatures of the studied chlorites from chromitites fall within the range of 250–284°C. Conclusions. Noble metal minerals from secondary associations were formed at temperatures below 350°C together with garnet, amphibole, chlorite, and nickel sulfides. Grains of primary Os–Ir–Ru alloys during epigenetic processes underwent sulfurization with the formation of a fine-grained porous mixture of native and sulfide (sometimes with As) phases, and replacement by Ru-pentlandite. The presence of awaruite and native Cu and Ni in both primary and secondary assemblages of chromotites indicates the reducing conditions for the formation of noble metal minerals. The limited occurrence of high-Cr ores, along with the manifested processes of sulfurization for primary grains of Os–Ir–Ru alloys, led to the scarcity of detrital PGM in the area of the Alapaevsk massif.

Genesis of Magmatic Albitite Related Hydrothermal Uranium Mineralisation in Geratiyon-ki-Dhani, Sikar District, Rajasthan: Evidences from Fluid Inclusion Studies

Abstract Geratiyon-ki-Dhani (GKD) area is located in Khetri sub-basin of North Delhi Fold Belt and exposes metasediments of Ajabgarh Group. The Ajabgarh Group comprises quartz-biotite schist which is intruded by albitite and granite. The primary uranium phases viz. davidite and brannerite occurring with calcite and /or quartz veins are common in albitite. Quartz and calcite from mineralised albitite have been selected for characterization of the ore-forming fluid, which makes a promising uranium deposit. Fluid inclusion petrography indicated presence of three (03) types of fluid inclusions (FIs) based on phases present at room temperature and mode of occurrence; polyphase (type 1a & 1b) and biphase (type 2) inclusions. Type 1a FIs are primary in nature and are composed of vapour bubble, salt crystals with <50% liquid phase and are irregular or negative crystal in shape varying in size between 12–23μm and occasionally contain hematite grain. The type 1a inclusions homogenised mostly by dissolution of salt crystal between 243-382°C (mode=340°C, n=30) corresponding to salinity of 34.32–46.13 wt% NaCl-eq (mode=42wt% NaCl-eq, n=30). Type 1b FIs have vapour bubble, salt crystal with > 50% liquid phase, occur as trans-granular trails and in clusters, having irregular shapes with size varying from <5–12μm. The inclusions homogenised by disappearance of salt crystals at 209 to 294°C (mode= 280°C, n=35) corresponding to salinity range from 29.03–38.59 wt% NaCl-eq (mode=36wt% NaCl-eq, n=35). A wide range of overlap is noted in salinity (34.32–38.59 wt% NaCl-eq) and homogenization temperature (243 – 294°C), histograms of type 1a & 1b inclusions suggest them to be part of a common fluid activity. Polyphase inclusions show simple cooling and follow halite saturation curve in salinity-temperature diagram. Biphase inclusions are invariably associated with type 1b and also show a cooling trend. On the basis of fluid characteristics, it is concluded that magmatic albitite has provided single mineralising solution resulting in davidite enriched mineralisation. The gradual cooling of high temperature (243- 382°C), high saline (34.32– 46.13 wt% NaC-leq) hydrothermal fluids has ensued U-mineralisation in GKD. The evidences presented here are significant as magmatic albitite hosted mineralisation is found for the first time in North Delhi Fold Belt of Khetri sub-basin of northwest India. It has opened a new concept for exploration which will help more resource addition.

Late Miocene magmatic‐hydrothermal system and related Cu mineralization of the Arakawa area, Akita, Japan

AbstractThe Northeast Japan arc hosts a number of hydrothermal vein‐type copper deposits associated with Neogene felsic intrusions. The Arakawa area is underlain by Cretaceous granites and Tertiary sedimentary rocks, which were intruded by the Miocene Ushizawamata dacite. Zircon grains from the dacite intrusion yield a 206Pb/238U intercept age (laser ablation inductively coupled plasma mass spectrometry) of 8.10 ± 0.30 Ma, consistent with a previously reported K‐Ar illite age (8.1 ± 0.4 Ma) of the Ushizawamata lead and zinc prospect in the Arakawa area. The dacite intrusion and the surrounding Miocene sedimentary rocks were altered by hydrothermal activity on the surface, classified into four alteration zones: (1) biotite‐chlorite, (2) illite, (3) chlorite and (4) smectite, centered on the intrusion. About 20 major vertical sub‐parallel copper‐bearing quartz veins occur in the chlorite alteration zone on the west side of the dacite. The first vein stage is composed of chalcopyrite and chamosite with a minor amount of quartz in brecciated wall rocks, and the second‐stage is characterized by the presence of hematite in addition to the first‐stage mineral assemblage. The third‐stage consists of comb‐shaped quartz veins with a minor amount of chalcopyrite, sphalerite, galena and pyrite, and the fourth‐stage of barite and apatite present in druse in the third‐stage veins. Primary fluid inclusions in quartz of the first‐ and third‐stages are all liquid‐rich and two‐phase. Homogenization temperature and salinity of first‐stage quartz are 263–277°C and 5.7–7.5 wt% NaCl equivalent (eq.); in quartz of the third‐stage, 251–270°C and 2.7–4.2 wt% in the inner zone and 207–250°C and 2.7–3.7 wt% in comb‐shaped quartz on the vein margin. The fluid inclusions in quartz phenocrysts of the Ushizawamata dacite show two distinct assemblages, halite‐bearing polyphase inclusions that coexist with vapor‐phase inclusions and/or vapor‐rich two‐phase inclusions, and liquid‐rich two‐phase inclusions. Homogenization temperature and salinity of the polyphase inclusions are higher than 401°C and 46.7 wt%, respectively, and those of the vapor‐rich two‐phase inclusions report 393–419°C and 2.6–3.7 wt% NaCl, whereas the liquid‐rich two‐phase inclusions returned 344–403°C and 8.0–9.3 wt%, respectively. These results indicate that the ore forming fluid was slightly cooler and lower in salinity than the late‐stage hydrothermal fluid in the Ushizawamata intrusion. The spatial and temporal proximity between the Ushizawamata dacite and the hydrothermal veins indicates that the dacitic magma was genetically related to the vein copper mineralization in the Arakawa area.

Melt- to Shear-Controlled Exhumation of Granulites in Granite–Gneiss Domes: Petrological Perspectives from Metapelite of the Neoarchean Ha-Tshanzi Structure, Central Zone, Limpopo Complex, South Africa

Abstract Gneiss domes cored by migmatites and granites represent the principal role of anatectic melts during the exhumation of high-grade metamorphic complexes. This study explores the exhumation history of a metapelitic granulite within the Ha-Tshanzi structure from the Central Zone of the Neoarchean–Paleoproterozoic Limpopo high-grade Complex, South Africa. Quartzofeldspathic garnet-bearing coarse-grained leucosomes in the rock alternate with attenuated shear bands consisting of biotite, cordierite, sillimanite and quartz that prominently modified the earlier garnet porphyroblasts. Cores of garnet porphyroblasts contain various polyphase inclusions that are interpreted as crystallized inclusions of melt. The phase equilibria modeling and regular zoning of garnet with respect to major (Mg, Fe, Ca) and some trace (P, Cr, Sc) elements reveals that a garnet + biotite + plagioclase + quartz ± sillimanite assemblage in the rock coexisted with the melt during the sub-isothermal (810–830 °C) exhumation from pressure of 10·0–10·2 kbar to 7·5–7·0 kbar during the Neoarchean event (2·68–2·62 Ga). The exhumation mediated by anatectic melt supports interpretation of the Ha-Tshanzi structure as a diapir-related granite–gneiss dome. During upwelling of the dome, the melt segregated into leucosome, while growth of cordierite sequestered water from the melt, assisting its crystallization at the end of the sub-isothermal decompression stage. As the rheology of the rock changed, melt-dominated deformation was transformed to solid-dominated ductile shear deformation. In contrast to the earlier sub-isothermal decompression P–T path, the gentler slope of ~75 °C kbar–1 of the decompression-cooling path marks the exhumation from pressures of ~7 kbar to pressures of 5–4·5 kbar and cooling to 600–550 °C. Dating of zircon, monazite and rutile shows that the Neoarchean evolution of the metapelite was strongly overprinted by the Paleoproterozoic event at c. 2·01 Ga. The results of the study highlight the significance of domed structures related to granitic diapirs in the exhumation of the Central Zone of the Limpopo Complex.

Redox-controlled chalcophile element geochemistry of the Polaris Alaskan-type mafic-ultramafic complex, British Columbia, Canada

ABSTRACT The Early Jurassic Polaris Alaskan-type intrusion in the Quesnel accreted arc terrane of the North American Cordillera is a zoned, mafic-ultramafic intrusive body that contains two main styles of magmatic mineralization of petrologic and potential economic significance: (1) chromitite-associated platinum group element (PGE) mineralization hosted by dunite (±wehrlite); and (2) sulfide-associated Cu-PGE-Au mineralization hosted by olivine (±magnetite) clinopyroxenite, hornblendite, and gabbro-diorite. Dunite-hosted PGE mineralization is spatially associated with thin discontinuous layers and schlieren of chromitite and chromitiferous dunite and is characterized by marked enrichments in iridium-subgroup PGE (IPGE) relative to palladium-subgroup PGE (PPGE). Discrete grains of platinum group minerals (PGM) are exceedingly rare, and the bulk of the PGE are inferred to reside in solid solution within chromite±olivine. The absence of Pt-Fe alloys in dunite of the Polaris intrusion is atypical, as Pt-enrichment of dunite-hosted chromitite is widely regarded as a characteristic feature of Alaskan-type intrusions. This discrepancy appears to be consistent with the strong positive dependence of Pt solubility on the oxidation state of sulfide-undersaturated magmas. Through comparison with experimentally determined PGE solubilities, we infer that the earliest (highest temperature) olivine-chromite cumulates of the Polaris intrusion crystallized from a strongly oxidized ultramafic parental magma with an estimated log f(O2) > FMQ+2. Parental magmas with oxygen fugacities more typical of volcanic arc settings [log f(O2) ∼ FMQ to ∼ FMQ+2] are, in turn, considered more favorable for co-precipitation of Pt-Fe alloys with olivine and chromite. More evolved clinopyroxene- and hornblende-rich cumulates of the Polaris intrusion contain low abundances of disseminated magmatic sulfides, consisting of pyrrhotite and chalcopyrite with minor pentlandite, pyrite, and rare bornite (≤12 wt.% total sulfides), which occur interstitially or as polyphase inclusions in silicates and oxides. The sulfide-bearing rocks are characterized by strong primitive mantle-normalized depletions in IPGE and enrichments in Cu-PPGE-Au, patterns that resemble those of other Alaskan-type intrusions and primitive arc lavas. The absolute abundances and sulfur-normalized whole-rock concentrations (Ci/S, serving as proxy for sulfide metal tenor) of chalcophile elements, including Cu/S, in sulfide-bearing rocks are highest in olivine clinopyroxenite. Sulfide saturation in the relatively evolved magmas of the Polaris intrusion, and Alaskan-type intrusions in general, appears to be intimately tied to the appearance of magnetite. Fractional crystallization of magnetite during the formation of olivine clinopyroxenite at Polaris resulted in reduction of the residual magma to log f(O2) ≤ FMQ+2, leading to segregation of an immiscible sulfide melt with high Cu/Fe and Cu/S, and high PGE and Au tenors. Continued fractionation resulted in sulfide melts that were progressively more depleted in precious and base chalcophile metals. The two styles of PGE mineralization in the Polaris Alaskan-type intrusion are interpreted to reflect the evolution of strongly oxidized, hydrous ultramafic parental magma(s) through intrinsic magmatic fractionation processes that potentially promote sulfide saturation in the absence of wallrock assimilation.

Intracrystalline melt migration in deformed olivine revealed by trace element compositions and polyphase solid inclusions

Abstract. Melt transport mechanisms have an important impact on the chemical composition of the percolated host rock and the migrating melts. Melt migration is usually assumed to occur at grain boundaries. However, microstructural studies revealed the occurrence of polyphase inclusions along dislocations, subgrain boundaries and microcracks in single mineral grains. The inclusions are interpreted as crystallized melt pockets suggesting that melts can migrate within deformed crystals. Intracrystalline melt migration and diffusive re-equilibration can lead to significant mineral trace element enrichments when associated with dissolution–precipitation reactions. In this contribution, we study a body of replacive troctolites associated with the Erro-Tobbio ophiolitic mantle peridotites (Ligurian Alps, Italy). The replacive formation of the olivine-rich troctolite involved extensive impregnation of a dunitic matrix, i.e. partial dissolution of olivine and concomitant crystallization of interstitial phases. The olivine matrix is characterized by two distinct olivine textures: (i) coarse deformed olivine, representing relicts of the pre-existing mantle dunite matrix (olivine1), and (ii) fine-grained undeformed olivine, a product of the melt–rock interaction process (olivine2). Previous studies documented a decoupling between olivine texture and trace element composition, namely enriched trace element compositions in olivine1 rather than in olivine2, as would be expected from the dissolution–precipitation process. Notably, the trace element enrichments in deformed olivines are correlated with the occurrence of elongated 10 µm size polyphase inclusions (clinopyroxene, Ti-pargasite, chromite) preferentially oriented along olivine crystallographic axes. These inclusions show irregular contacts and have no crystallographic preferred orientation with the host olivine, and the phases composing the inclusions show similar chemical compositions to the vermicular phases formed at the grain boundaries during late-stage reactive crystallization of the troctolite. This suggests that the investigated inclusions did not form as exsolutions of the host olivine but rather by input of metasomatic fluids percolating through the deformed olivine grains during closure of the magmatic system. We infer that strongly fractionated volatile-rich melts were incorporated in oriented microfractures within olivine1 and led to the crystallization of the polyphase inclusions. The presence of intracrystalline melt greatly enhanced diffusive re-equilibration between the evolved melt and the percolated olivine1, in turn acquiring the enriched character expected in neoformed olivine crystals. Intracrystalline melt percolation can have strong geochemical implications and can lead to efficient re-equilibration of percolated minerals and rocks.

Mineralogy and Fluid Inclusions of the Cunas Emerald Mine, Maripí, Boyacá, Colombia

The Cunas mine is currently one of the major producers of fine emeralds in Colombia; its emeralds typically display a magnificent green hue, which is highly appreciated in the world market. The mineralization is found in vanadium-rich black shales of the Muzo formation; emeralds occur in pockets within hydrothermal veins and breccias, consisting mostly of calcite, dolomite, albite, quartz, and minor pyrite, parisite-(Ce), and fluorite; hydrothermal alteration is pervasive and dominated by albitization and carbonatization. Emerald-hosted fluid inclusions are highly abundant and remarkably large and complex. Poly-phase inclusions are ubiquitous, occur both in emeralds and gangue minerals, and consist of two daughter crystals (typically halite and calcite or siderite; exceptionally parisite-(Ce)), a liquid brine, a CO2-N2-CH4-rich gas bubble, and occasionally minor liquid CO2. Vapor-rich inclusions were observed in quartz, and two-phase inclusions were identified in calcite and dolomite, thus suggesting a complex fluid evolution. Microthermometry analysis indicates the emerald-forming fluids were trapped at relatively low temperature ≈ 260-340°C and pressure ≈ 875-2400 kbar, with relatively high density —1.03 g/cm³—, and elevated salinity 39% NaCl eq. Wt.; other aqueous components detected include CaCl2, KCl, and FeCl2. Based on these data, we propose the emerald mineralization at the Cunas mine was originated by the mixing of two hydrothermal fluids of different sources; one fluid with high salinity derived from evaporite dissolution, responsible for the albitization of the host rocks; the second is a calcium-rich fluid evolved from connate waters, which was equilibrated by the interaction with calcareous and organic-rich wall rocks. As a result, emerald mineralization took place at structurally favorable sites where fluid mixing was promoted. The described geological and physicochemical features for the Cunas mine, are in agreement with an epigenetic sediment-hosted mineralization —Colombian-type— formed by the circulation and mixing of relatively low-temperature non-magmatic fluids.

A siliceous komatiitic source of Bushveld magmas revealed by primary melt inclusions in olivine

Our experimental thermobarogeochemical study of the primary melt inclusions in olivine (Fo91) from poikilitic harzburgite to dunite of the Uitkomst Complex in the Bushveld Igneous Province revealed a series of melt compositions that are the result of combined fractional crystallization and assimilation. The primary melt inclusions up to 50 μm in size are fully crystallized and composed of predominantly olivine and orthopyroxene with highly subordinate chromite, sulfide, amphibole and plagioclase accompanied by a fluid phase in shrinkage voids. The most primitive melt within the series has a re-homogenization temperature of >1450 °C and contains 22.47 wt% MgO, 12.57 wt% FeO, 51.90 wt% SiO2, 2.50 wt% CaO, 8.27 wt% Al2O3 and 1.69 wt% Na2O recalculated to equilibrium with the host olivine. This is the first direct measurement of the komatiitic parental magma of the Bushveld magmas, inferred in previous studies. The estimated maximum PT parameters of the melt corresponds to 2.5 GPa and 1590 °C implying that the primitive melt inclusions in the olivine were trapped while still in the upper mantle and before further crustal assimilation. This primitive melt shows the steepest slope (La/Yb)PM, the highest Ni and is depleted in volatile components (168 ppm H2O, 264 ppm Cl, 258 ppm F and 114 ppm S according to secondary ion mass spectrometry measurements) compared to more evolved compositions, which were progressively enriched in volatiles up to 7665 ppm Н2О, 1728 ppm Cl, 2288 ppm S, and 549 ppm F as the rehomogenization temperature fell to 1335 °C. The progressive assimilation of crustal material responsible for magma modification is also manifested by the occurrence of CaNa volatile-rich minerals (such as amphibole, phlogopite, albite, sodalite, natrolite, pectolite, Cl-apatite and carbonate) in the interstitial assemblage and in “exotic” polyphase inclusions in cumulus olivine.The concentrations and ratios of the incompatible elements in the melt inclusions in Uitkomst olivine are similar to those in the model compositions of the ultramafic Bushveld parental magma and support a common source of ultramafic melts in the Bushveld Province. The main components of the melts, however, are not in accord with either boninitic or komatiitic lineages indicating a unique nature for the Bushveld magmas.

Garnet sand reveals rock recycling processes in the youngest exhumed high- and ultrahigh-pressure terrane on Earth

Rock recycling within the forearcs of subduction zones involves subduction of sediments and hydrated lithosphere into the upper mantle, exhumation of rocks to the surface, and erosion to form new sediment. The compositions of, and inclusions within detrital minerals revealed by electron microprobe analysis and Raman spectroscopy preserve petrogenetic clues that can be related to transit through the rock cycle. We report the discovery of the ultrahigh-pressure (UHP) indicator mineral coesite as inclusions in detrital garnet from a modern placer deposit in the actively exhuming Late Miocene-Recent high- and ultrahigh-pressure ((U)HP) metamorphic terrane of eastern Papua New Guinea. Garnet compositions indicate the coesite-bearing detrital garnets are sourced from felsic protoliths. Carbonate, graphite, and CO2 inclusions also provide observational constraints for geochemical cycling of carbon and volatiles during subduction. Additional discoveries include polyphase inclusions of metastable polymorphs of SiO2 (cristobalite) and K-feldspar (kokchetavite) that we interpret as rapidly cooled former melt inclusions. Application of elastic thermobarometry on coexisting quartz and zircon inclusions in six detrital garnets indicates elastic equilibration during exhumation at granulite and amphibolite facies conditions. The garnet placer deposit preserves a record of the complete rock cycle, operative on <10-My geologic timescales, including subduction of sedimentary protoliths to UHP conditions, rapid exhumation, surface uplift, and erosion. Detrital garnet geochemistry and inclusion suites from both modern sediments and stratigraphic sections can be used to decipher the petrologic evolution of plate boundary zones and reveal recycling processes throughout Earth's history.

Formation of Chromitite Seams and Associated Anorthosites in Layered Intrusion by Reactive Volatile-rich Fluid Infiltration

Abstract Drilling related to development of the platinum-group element deposit of the J-M Reef of the Stillwater Complex returned samples of a rare chromitite seam between anorthosite and norite in a discordant anorthositic body. Plagioclase core An concentrations are marginally higher and modestly reversely zoned on the norite side (average Ancore = 83·8; average Ancore – Anrim = –1·1) as compared with the anorthosite side (average Ancore 82·5; average Ancore – Anrim = +1·0). The anorthosites are also characterized by a slightly smaller average plagioclase grain size than plagioclase in the norite (1·41 mm and 1·54 mm, respectively). The chromite can contain single and polyphase inclusions of orthopyroxene, plagioclase, amphibole, biotite and Cl-rich apatite. These and other compositional and textural features, as well as inference from other discordant anorthositic bodies in the Banded series, are all consistent with a chromatographic model of chromite precipitation at a reaction front as a norite protolith reacts with a Cl-rich aqueous fluid saturated in plagioclase alone. Chromitite seam formation is modeled using an infiltration metasomatic model, in which a fluid becomes progressively undersaturated in pyroxene as it rises into the hotter part of the crystal pile. As this pyroxene-undersaturated fluid moves through a noritic protolith, it dissolves the Cr-bearing orthopyroxene to produce an anorthosite. Chromite precipitates at the reaction front between the anorthosite and the norite owing to liberation of Mg and Cr from pyroxene. Continuous redissolution and reprecipitation of chromite occurs as the pyroxene dissolution front moves in the direction of fluid flow, collecting the Cr lost from the anorthosite. Owing to Cr dissolved mainly as a neutral divalent cation complex, CrCl(OH)0, in the solution, but incorporated as a trivalent cation in chromite, the required redox reaction can involve concurrent precipitation of sulfide with chromite. This mechanism differs from some recent models in that the anorthosites are themselves replacement bodies and are not original precipitates from a magma nor formed by loss of mafic material by partial melting. The results show the need for experimental mineral solubility data at T and P conditions appropriate to upper crustal mafic–ultramafic intrusions.

Brittle Deformation During Eclogitization of Early Paleozoic Blueschist

The Tsäkkok Lens of the Scandinavian Caledonides represents the outermost Baltican margin that was subducted in late Cambrian/Early Ordovician time during closure of the Iapetus Ocean. The lens predominantly consists of metasedimentary rocks hosting eclogite bodies that preserve brittle deformation on the μm-to-m scale. Here, we present a multidisciplinary approach that reveals fracturing related to dehydration and eclogitization of blueschists. Evidence for dehydration is provided by relic glaucophane and polyphase inclusions in garnet consisting of clinozoisite + quartz ± kyanite ± paragonite that are interpreted as lawsonite pseudomorphs. X-Ray chemical mapping of garnet shows a network of microchannels that propagate outward from polyphase inclusions. These microchannels are healed by garnet with elevated Mg relative to the surrounding garnet. Electron backscatter diffraction mapping revealed that Mg-rich microchannels are also delimited by low angle (&amp;lt;3°) boundaries. X-ray computed microtomography demonstrates that some garnet is transected by up to 300 μm wide microfractures that are sealed by omphacite ± quartz ± phengite. Locally, mesofractures sealed either by garnet- or omphacite-dominated veins transect through the eclogites. The interstices within the garnet veins are filled with omphacite + quartz + rutile + glaucophane ± phengite. In contrast, omphacite veins are predominantly composed of omphacite with minor apatite + quartz. Omphacite grains are elongated along [001] crystal axis and are preferably oriented orthogonal to the vein walls, indicating crystallization during fracture dilation. Conventional geothermobarometry using omphacite, phengite and garnet adjacent to fractures, provides pressure-temperature conditions of 2.47 ± 0.32 GPa and 620 ± 60°C for eclogites. The same method applied to a mesoscale garnet vein yields 2.42 ± 0.32 GPa at 635 ± 60°C. Zirconium-in-rutile thermometry applied to the same garnet vein provides a temperature of ∼620°C. Altogether, the microchannels, microfractures and mesofractures represent migration pathways for fluids that were produced during glaucophane and lawsonite breakdown. The microfractures are likely precursors of the mesoscale fractures. These dehydration reactions indicate that high pore-fluid pressure was a crucial factor for fracturing. Brittle failure of the eclogites thus represents a mechanism for fluid-escape in high-pressure conditions. These features may be directly associated with seismic events in a cold subduction regime.

Fluid Evolution of the Čukaru Peki Cu-Au Porphyry System (East Serbia) inferred from a fluid inclusion study

Čukaru Peki is a recently discovered copper-gold deposit in the Bor metallogenic zone in east Serbia. Three types of mineralization can be distinguished in this ore deposit: porphyry, high-sulphidation, and transitional epithermal type. This research was focused on fluid inclusion analysis of genetically different veins from the porphyry and the transitional zones of Čukaru Peki with an aim of better understanding the fluid evolution and mineralization processes in this system. Seven types of veins were identified in the porphyry zone of Čukaru Peki and four of these veins contained transparent minerals which were suitable for fluid inclusion analysis. Eight types of inclusion assemblages were distinguished in these veins: type 1 – primary inclusions with homogenization temperatures above 550°C and high salinity, type 2a- scattered polyphase inclusions two salt crystals, type 2b-polyphase inclusions with two salt crystals in crystal growth zones, type 3- brine inclusions with one salt crystal in crystal growth zones, type 4- vapour-rich inclusions, type 5- primary inclusions in anhydrite, and types 6 and 7- secondary low-temperature inclusions This research suggests that saline fluids (30-40% wt.% NaCl eq.) were the most important ones for the formation of porphyry-type mineralization and that the mineralization was formed at temperatures between 350 and 450°C and pressures between 100 and 500 bars. The epithermal stage was characterized by cooler low-salinity fluids with temperatures between 150-350°C, and salinity between 0 and 7 wt.% NaCl eq.

Evolution of a gneiss in the Seve nappe complex of central Sweden – Hints at an early Caledonian, medium-pressure metamorphism

Ultrahigh-pressure (UHP) metamorphism has recently been reported from various crustal rocks in the Seve nappe complex (SNC) in which microdiamonds were found. We studied a gneiss from the Åreskutan Nappe in central Sweden. This nappe of the SNC was recently interpreted to have experienced UHP metamorphism. The studied medium-grained and well foliated gneiss contains quartz, biotite, garnet, K-feldspar, plagioclase, and potassic white mica with accessory kyanite, sillimanite, rutile, ilmenite, and monazite. Pressure (P) – temperature (T) pseudosections were mainly used to decipher the metamorphic evolution of the gneiss. According to polyphase inclusions such as biotite + chlorite + potassic white mica in the garnet core, the prograde P-T conditions were approximately 600 °C and 8–8.5 kbar. An isobaric heating to 700 °C followed, constrained by homogenous garnet with XCa = 0.03 and XMg = 0.295, the highest Si content of 3.15 per formula unit in potassic white mica, and Zr-in-rutile thermometry. A late migmatitic stage occurred at about 725 °C and 6.5 kbar. U-Th-Pb dating of monazite, included in garnet, with the electron microprobe yielded two populations at 463 ± 12(2σ) Ma (Y2O3 > 2.0 wt%) and 458 ± 7(2σ) Ma (Y2O3 < 0.5 wt%) that were assigned to the prograde evolution before and during/after garnet growth. A matrix population gave 448 ± 12(2σ) Ma (Y2O3 < 0.5 wt%) which we relate to the late migmatitic stage. We hypothesize that the studied rock experienced prograde metamorphism in the uppermost portion of a downgoing continental plate (Baltoscandia) by thrusting under an island arc/microcontinent. Afterwards, the rock was exhumed by mass flow in an exhumation channel during the early Caledonian orogeny.

Quantitative PIXE analyses of trace Ti in single fluid inclusions in quartz from Tsushima granite

The trace element content of single fluid inclusions in quartz from Tsushima granite in Japan was determined with particle-induced X-ray emission (PIXE) to investigate the chemical features of Ti in hydrothermal fluids derived from granites. Most of the fluid inclusions were polyphase and vapor-rich fluid inclusions, and both types contained Cl, K, Ca, Ti, Mn, Fe, Ni, Cu, Zn, Ge, Br, Rb, Sr, Ba, and Pb. Concentrations of Ti were of up to a few tens ppm wt Ti for polyphase inclusions and up to one hundred ppm for vapor-rich fluid inclusions. The Ti content indicated the possibility of transportation of a certain amount of Ti by granitic hydrothermal fluids.

Monazite behaviour during metamorphic evolution of a diamond-bearing gneiss: a case study from the Seve Nappe Complex, Scandinavian Caledonides

Abstract Monazite is a common mineral in metapelitic rocks including those which underwent ultra-high pressure (UHP) metamorphism. During metamorphic evolution monazite adapts its composition to the changing mineral assemblage, especially in its heavy rare earth element contents. We studied this process in diamond-bearing gneiss containing monazite, from Saxnäs in the Seve Nappe Complex of the Scandinavian Caledonides. Although the rock has been re-equilibrated under granulite facies and partial melting conditions, it still preserves minerals from the UHP stage: garnet, kyanite, rutile, and especially diamond. Microdiamonds occur in situ as inclusions in garnet, kyanite and zircon, either as single-crystals or polyphase inclusions with Fe-Mg carbonates, rutile and CO2. Both monazite and diamond occur in the rims of garnet showing the highest pyrope content and a secondary peak of yttrium. Such a position indicates thermally activated diffusion under high temperature at the end of prograde metamorphism. Monazite compositions show negative Eu anomalies, which we interpret to be inherited from the source rock, not reflecting the coexistence with plagioclase and/or K-feldspar which are unstable at UHP conditions. Our results suggest that the effect of whole-rock composition may be more important than that of coexisting phases. The UHP monazite was most likely formed from allanite during subduction and prograde metamorphism. The monazites included in garnet and kyanite are mostly unaltered, whereas those in the matrix show breakdown coronas consisting of apatite, REE-epidote/allanite and REE carbonate, likely formed due to pressure decrease and cooling. U-Th-Pb chemical age dating of monazites yields an isochron centroid age of 472 ±3 Ma. We interpret this age as monazite growth under UHP conditions related to subduction of the Baltica continental margin in Early Ordovician time.

Carbonate-silicate inclusions in garnet as evidence for a carbonate-bearing source for fluids in leucocratic granitoids associated with granulites of the Southern Marginal Zone, Limpopo Complex, South Africa

We present a study of carbonate-bearing polyphase inclusions in garnets from leucocratic granitoids intruding metapelitic granulites of the Southern Marginal Zone (SMZ) of the Neoarchean Limpopo high-grade complex, South Africa, during the post-peak stage (2710–2650 Ma; U-Pb ages for zircons and monazites). Ternary feldspar thermometry suggests that the granitoid magma cooled from temperatures 800–900 °C at a pressure of ca. 6.5 kbar. Abundant CO2 fluid inclusions in quartz and T-XCO2 phase equilibria modeling via PERPLE_X imply action of an essentially carbonic fluid in the granitoids. Cores of almandine-rich garnet grains from the granitoids contain polyphase carbonate-bearing inclusions with a distinct negative crystal shape. The major carbonate in the inclusions is a strongly zoned magnesite-siderite variety, whereas pyrophyllite is the predominant silicate phase. Raman spectra of unexposed inclusions revealed a presence of CO2, as well as CH4 and H2O. The carbonate-bearing inclusions coexist with larger polyphase inclusions composed of biotite, quartz, K-feldspar, plagioclase, sillimanite, which are interpreted as relics of granitic melts. Modeling the mineral assemblage preserved within the carbonate-bearing inclusions shows that their present mineral and chemical compositions are a product of interaction of the trapped aqueous‑carbonic fluid with host garnet during cooling below 400 °C. Despite strong modifications, the inclusions bear evidence for initial saturation of the fluid with Mg‑carbonate. This is taken as an evidence for an origin of the fluids by devolatilization of the Mg-rich carbonate-bearing ultrabasic greenstone rocks of the Kaapvaal Craton that were buried under the SMZ. Being generated at temperatures between 650 and 700 °C, the fluid subsequently participated in anatexis and coexisted with the granite magma during exhumation and interaction of the SMZ granulites with cratonic rocks.

Cr-spinel assemblage from the Upper Triassic gritstones of the northeastern Siberian Platform

An assemblage of Cr-spinels widespread in Carnian (Upper Triassic) diamondiferous deposits in the northeastern Siberian Platform is studied. Analysis of their morphology and chemical composition has revealed two dominant varieties of Cr-spinels and has demonstrated certain regularities in their distribution in the study area. Correlations have been established between the areal distribution of the recognized types of Cr-spinels and diamond varieties typical of kimberlite sources and between the distribution of Cr-spinels and rounded diamond dodecahedrons. The phase and chemical compositions of polyphase inclusions in the Cr-spinels are studied. The spatial arrangement of inclusions along the crystal growth zones indicates their primary genesis and trapping from the melt during crystallization. Compositional features of some minerals in the inclusions—SiO2 impurity in apatite and high CaO contents (0.2-0.8 wt.%) in olivines—point to a nonkimberlite source of these Cr-spinels. The presence of K- and Na-containing phases and calcite in the inclusions indicates saturation of the initial melt with alkalies, Ca, and CO2. The data obtained suggest that the numerous Late Vendian diatremes in K-rich alkaline basites of the Olenek Uplift area are the source of the dominant Cr-spinel variety.

Solid solutions in the system acanthite (Ag2S)–naumannite (Ag2Se) and the relationships between Ag-sulfoselenides and Se-bearing polybasite from the Kongsberg silver district, Norway, with implications for sulfur–selenium fractionation

Sulfoselenides [Ag2(S,Se)] and Se-bearing polybasite have been discovered at the Kongsberg silver district. The selenium-bearing minerals occur in two samples from the northern part of the district, forming either single or polyphase inclusions together with chalcopyrite within native silver. The Ag-sulfoselenides show large chemical variations, covering nearly the complete compositional range between acanthite (Ag2S) and naumannite (Ag2Se). For the data presented here, there is no local maximum at the composition Ag4SSe attributed to the distinct phase called aguilarite, suggesting that this composition can be considered as one of many possible along the monoclinic Ag2S–Ag2S0.4Se0.6 solid solution series rather than a specific mineral phase. We present a model explaining the variations in the Se-content of Ag2(S,Se) as a result of gradual de-sulfidization of the rock under oxidizing conditions. During this process, sulfur from the Ag2S-component of Ag2(S,Se) oxidized and dissolved in the fluid phase as SO42−, resulting in the formation of native silver. The activity ratio $${a_{{{\text{S}}^{2 - }}}}/{a_{{\text{S}}{{\text{e}}^{2 - }}}}$$ of the system gradually decreased due to the removal of SO42−, which resulted in the stabilization of a sulfoselenide with higher selenium content. As a result of reaction progress, grains of Ag2(S,Se) became gradually enclosed in newly formed native silver, and therefore isolated from further reactions with the grain-boundary fluid. Grains isolated early during the process show low content of Se reflecting high $${a_{{{\text{S}}^{2 - }}}}/{a_{{\text{S}}{{\text{e}}^{2 - }}}}$$ of the equilibrium fluid, while grains showing high Se reflect the composition of late low $${a_{{{\text{S}}^{2 - }}}}/{a_{{\text{S}}{{\text{e}}^{2 - }}}}$$ fluids. Analyses of Se-bearing polybasite show that selenium is preferentially partitioned into Ag2(S,Se) compared to polybasite. The model presented here demonstrates how oxidation of sulfoselenides leads to fractionation of sulfur and selenium.