A TEM Study on Fluid Inclusions in Coesite-bearing Jadeite Quartzite in Shuanghe in the Dabie Mountains

Fluid inclusions at a nano to sub-micron scale in quartz from jadeite quartzite at Shuanghe, Dabie Mountains, have been investigated by using the transmission electron microscopy (TEM). Most fluid inclusions are spherical or negative crystal shaped, forming wide swarm-like trails. The TEM reveals that the relationship between coesite and the host quartz is syntaxic and provides strong evidence of the occurrence of high-salty fluids at peak metamorphic conditions. The fluid inclusions are often connected to dislocations, which are undetected at the scale of optical microscopy. Non-decrepitation leakage of fluid inclusions may occur by pipe diffusion of molecule H2O or CO2 along dislocations from the inclusions into the host quartz, thus leading to original inclusion density and composition changes. It should be taken into full account for the correct petrological interpretation of micro-thermometric results.     

大别山双河硬玉石英岩石英中的纳米-亚微米级流体包裹体

用透射电子显微镜(TEM)观察产于大剐山双河地区含柯石英硬玉石英岩矿物石英中纳米级至亚微米级的流体包裹体超微观结构特征发现：大多数包裹体呈圆形或负晶形(粒径大多为10nm～350nm),构成宽的密集的包裹体串。TEM揭示了柯石英和寄主矿物石英之间为共晶格取向连生关系,并寻找到在峰期变质条件下高盐流体存在的有力证据。流体包裹体经常伴随着许多相互连接的位错,并且与位错和位错壁等交生在一起,形成网络分布,这是在光学显微镜尺度下所不能探测到的。非爆裂的流体渗漏可能通过H2O或CO2分子沿位错的管道扩散,从包裹体进入寄主矿物石英,因而导致原来包裹体密度和成分的变化。     

Chemical and isotopic effects of retrogression in metamorphic fluid inclusions

Fluid inclusions may provide compositional and isotopic information about fluids from which the host mineral precipitated as long as the host mineral does not react with the fluid. Our transmission electron microscope (TEM) investigation of grain boundaries and of fluid inclusions in zoisite and quartz of high-pressure metamorphic rocks from Dabie Shan (eastern China) demonstrates daughter minerals, such as margarite, muscovite, calcite, and anhydrite. Their precipitation changes (1) the composition of the fluid by selective and mineral-specific removal of CO₂ (carbonates), H₂O (sheet silicates, hydration of the walls), or S (gypsum, anhydrite, sulfides), (2) the concentrations and proportions of ions dissolved in the fluid, and (3) the isotopic composition of the fluid because of isotopic fractionation between mineral precipitate and fluid and between unmixed fluids. Fluid leakage from overpressurized fluid inclusions with daughter minerals changes the overall chemical and isotopic composition of the inclusion irreversibly, even when the daughter crystals later redissolve. Such fluid loss yields a wide range of compositionally and isotopically different fluids from a single starting fluid. Depending on the relation between mineral reactions in and fluid loss from the inclusion, the fluid remaining in the inclusion and the fluid lost from the inclusion may appear entirely unrelated.     

Crystallization and resorption in plutonic plagioclase: Implications on the evolution of granodiorite magma (Gęsiniec granodiorite, Strzelin Crystalline Massif, SW Poland)

Granodiorite from the Gęsiniec Intrusion, Strzelin Crystalline Massif, SW Poland contains complexly zoned plagioclases. Five chemically and structurally distinct zones can be correlated among crystals: ‘cores’ (25–35% An), inner mantles (40–45% An), outer mantles (40–25% An), resorption zones (35–50% An) and rims (35–30% An). Good structural and chemical (major and trace elements) correlation of zones between crystals indicates that zonation was produced by changes in conditions of crystallization on a magma chamber scale. Plagioclase, being the liquidus phase, records a time span from the beginning of crystallization to emplacement and rapid cooling of granodiorite as thin dykes.

Crystallization began with the formation of inner mantles. The paucity and different sizes of inner mantles suggests slow crystallization in high temperature magma. Normally zoned inner mantles were formed under increasing undercooling. Compositional trends in mantles suggest closed system crystallization.

The major resorption zones were caused by injection of less evolved magma as indicated by the strontium increase in plagioclase. The injection triggered a rapid rise of magma and plagioclase crystals facilitating mixing but also inducing fast, kinetically controlled growth of complex multiple, oscillatory zonation within resorption zones. The ascent of magma caused decompression melting of plagioclase and produced melt inclusions within inner mantles—the ‘cores’. The decompression range is estimated at a minimum of 2 kbar. Emplacement of granodiorite as thin dykes allow rapid cooling and preservation of magmatic zonation in plagioclases. Melt inclusions crystallized completely during post-magmatic cooling.

The zonation styles of plutonic plagioclase differ markedly from volcanic ones suggesting different magma evolution. Zones in plutonic plagioclase are well correlated indicating crystallization in quiescent magma where crystals accumulation and compositional magma stratification may occur. Crystals probably did not travel between different regimes. Resorption occurred but as single albeit complex episodes. Good correlation of zones in plutonic plagioclases allows a distinction between the main processes controlling zonation and superimposed kinetic effects.     

Submicron-sized fluid inclusions and distribution of hydrous components in jadeite,quartz and symplectite-forming minerals from UHP jadeite–quartzite in the Dabie Mountains,China: TEM and FTIR investigation

Fluid inclusions and clusters of water molecules at nanometer-to submicron-scale in size have been investigated using transmission electron microscopy (TEM) and Fourier transform infrared spectroscopy (FTIR) in jadeite, quartz and symplectite aegirine–augite, albite, taramite and magnetite corona minerals from ultrahigh-pressure (UHP) jadeite–quartzite at Shuanghe, the Dabie Mountains, China. Fluid inclusions from 0.003 μm to 0.78 μm in size occur in jadeite and quartz crystals, and a small number of fluid inclusions from 0.001 μm to 0.25 μm have also been detected in symplectite-forming minerals. Most of the fluid inclusions have round or negative crystal morphology and contain aqueous fluids, but some contain CO₂-rich fluids. They are usually connected to dislocations undetectable at an optical scale. The dislocations represent favorable paths for fluid leakage, accounting for non-decrepitation of most fluid inclusions when external pressure decreased at later stages, although there was partial decrepitation of some fluid inclusions unconnected to defect microstructures resulting from internal overpressure. Non-decrepitation and partial decrepitation of fluid inclusions resulted in changes of original composition and/or density. It is clear that identification of hidden re-equilibration features has significant implications for the petrological interpretation of post-peak metamorphic processes. Micro-FTIR results show that all jadeite and quartz samples contain structural water occurring as hydroxyl ions (OH⁻) and free water (H₂O) in the form of clusters of water molecules. The H₂O transformed from OH⁻ during exhumation and could have triggered and enhanced early retrograde metamorphism of the host rocks and facilitated plastic deformation of jadeite and quartz grains by dislocation movement, and thus the H₂O released during decompression might represent early-stage retrograde metamorphic fluid. The nominally anhydrous mineral (NAM) jadeite is able to transport aqueous fluids in concentrations of at least several hundred ppm water along a subduction zone to mantle depths in the form of clusters of water molecules and hydroxyl ions within crystals.     

Carbonatite melt–CO2 fluid inclusions in mantle xenoliths from Tenerife, Canary Islands: a story of trapping, immiscibility and fluid–rock interaction in the upper mantle

Three types of fluid inclusions have been identified in olivine porphyroclasts in the spinel harzburgite and lherzolite xenoliths from Tenerife: pure CO₂ (Type A); carbonate-rich CO₂–SO₂ mixtures (Type B); and polyphase inclusions dominated by silicate glass±fluid±sp±silicate±sulfide±carbonate (Type C). Type A inclusions commonly exhibit a “coating” (a few microns thick) consisting of an aggregate of a platy, hydrous Mg–Fe–Si phase, most likely talc, together with very small amounts of halite, dolomite and other phases. Larger crystals (e.g. (Na,K)Cl, dolomite, spinel, sulfide and phlogopite) may be found on either side of the “coating”, towards the wall of the host mineral or towards the inclusion center. These different fluids were formed through the immiscible separations and fluid–wall-rock reactions from a common, volatile-rich, siliceous, alkaline carbonatite melt infiltrating the upper mantle beneath the Tenerife. First, the original siliceous carbonatite melt is separated from a mixed CO₂–H₂O–NaCl fluid and a silicate/silicocarbonatite melt (preserved in Type A inclusions). The reaction of the carbonaceous silicate melt with the wall-rock minerals gave rise to large poikilitic orthopyroxene and clinopyroxene grains, and smaller neoblasts. During the metasomatic processes, the consumption of the silicate part of the melt produced carbonate-enriched Type B CO₂–SO₂ fluids which were trapped in exsolved orthopyroxene porphyroclasts. At the later stages, the interstitial silicate/silicocarbonatite fluids were trapped as Type C inclusions. At a temperature above 650 °C, the mixed CO₂–H₂O–NaCl fluid inside the Type A inclusions were separated into CO₂-rich fluid and H₂O–NaCl brine. At T<650 °C, the residual silicate melt reacted with the host olivine, forming a reaction rim or “coating” along the inclusion walls consisting of talc (or possibly serpentine) together with minute crystals of NaCl, KCl, carbonates and sulfides, leaving a residual CO₂ fluid. The homogenization temperatures of +2 to +25 °C obtained from the Type A CO₂ inclusions reflect the densities of the residual CO₂ after its reactions with the olivine host, and are unrelated to the initial fluid density or the external pressure at the time of trapping. The latter are restricted by the estimated crystallization temperatures of 1000–1200 °C, and the spinel lherzolite phase assemblage of the xenolith, which is 0.7–1.7 GPa.     

Evolution of metamorphic fluids in shear zones: The record from the emeralds of Habachtal, Tauern Window, Austria

Fluid inclusions in emeralds from the Habachtal, Central Tauern Window, have been studied by microthermometry. Results allow a detailed reconstruction of trapping history and evolution of the metamorphic fluids during the Middle Alpine Tauernkristallisation metamorphic event and some of the subsequent cooling period. Five different types of fluid inclusions, corresponding to at least five trapping periods, have been distinguished. In general, the earliest primary (type 1) inclusions, which occur as negative crystals or thin long tubes, are represented by low salinity ( < 10 wt. % NaCl equivalent) aqueous fluids with or without CO₂ with up to X_CO2 ≈ 0.04. Later primary type 2 inclusions are distinguished by different morphologies and distribution patterns. Lower salinity CO₂-free brines and CO₂-bearing denser inclusions with higher CO₂ contents (up to X_CO2 ≈ 0.11) are characteristic of this stage. The type 2 inclusions may also occur as pseudosecondary arrays. The effects of necking have been studied, and found to be considerable in the type 1 primary inclusions. This mechanism has occasionally resulted in the appearance of almost pure CO₂ fluids. The possibility of fluid immiscibility has been examined, and rejected, for the apparent “coexistence” of primary brine and CO₂-bearing inclusions. Instead, mixing of fluids which fluctuated between two different compositions is proposed. The fluctuation was probably due to the sequence of hydration reactions during the Tauernkristallisation. Maximum trapping pressures (3.6 kbar) obtained for stage 1 of the Tauernkristallisation are thought to represent a situation where sublithostatic fluid pressures exested in shear zones during the crystallisation period of many of the emerald cores and coexisting biotite and actinolite. Maximum fluid pressures of 7 kbar were obtained from the type 2 inclusions. This is similar to pressure estimates obtained from mineral equilibria. At least four phases of deformation are indicated by the trapping history. A pressure-temperature-time path for the Tauernkristallisation and the subsequent cooling/uplift period has been constructed for the Habachtal area, using the maximum pressure estimates obtained in this work together with previously existing data. In the cooling period, fluid pressures lower than the lithostatic load again prevailed. This difference, about 1–2 kbar, was probably due to late stage fracturing and/or the development of an open system. At least two more phases of minor deformation and three more stages of entrapment have been defined for this period. During this time, fluids gradually evolved towards more CO₂-poor, and less saline compositions. The present work shows that the possibility of fluctuations in fluid pressures must be considered seriously when attempting to define the PT cooling path from fluid inclusions in metamorphic rocks, especially those in shear zones. Postulations of retrograde PT paths based on fluid inclusions alone may result in pressure estimates which are too low.     

A possible UHP-eclogite in the Leaota Mts. (South Carpathians) and its history from high-pressure melting to retrograde inclusion in a subduction melange

An unusual eclogite pod containing impure jadeite to omphacite pyroxene with anti-phase domain (APD) visible under the optical microscope is hosted in a medium-grade matrix in the Leaota Massif. Textural relationships support the hypothesis of garnet formation by peritectic reactions involving high-jadeite clinopyroxene, while inclusions entrapped in garnet, mainly a wide range of amphibole compositions, seemingly crystallised from a fluid phase in disequilibrium with the garnet host. Thermobarometric estimates indicate UHP, HT peak conditions (2.8–3.2 GPa, 780–840°C) inconsistent with those of the associated rocks, followed by a complicated exhumation path. The P–T-array of the retrograde path suggests syn-subduction exhumation and tectonic inclusion in a melange with a matrix derived from the accretionary wedge. Partial melting of the subducting slab, which induces tectonic weakening, may be an effective mechanism in detaching and enclosing small eclogite pods in metamorphic terrains.     

阿尔泰伟晶岩中流体熔融包裹体成分的研究

对阿尔泰可可托海、柯鲁木特和库威伟晶岩锂辉石及绿柱石中单个流体熔融包裹体各相成分，借助激光拉曼探针进行分析，鉴定出固体相为不同硅酸盐子晶矿物，定量给出了流体相成分。根据子晶矿物和流体相成分估算了整个流体熔融包裹体的成分，并据此进一步讨论了熔体中流体的溶解度问题。流体熔融包裹体成分研究表明熔体中流体已达饱和或过饱和，流体相与熔体相发生分离，相应残余伟晶岩浆体系进入晶体＋熔体＋流体三相共存的岩浆－热液     

A reassessment of models for hydrocarbon generation in the Khibiny nepheline syenite complex, Kola Peninsula, Russia

Although hydrocarbon-bearing fluids have been known from the alkaline igneous rocks of the Khibiny intrusion for many years, their origin remains enigmatic. A recently proposed model of post-magmatic hydrocarbon (HC) generation through Fischer-Tropsch (FT) type reactions suggests the hydration of Fe-bearing phases and release of H₂ which reacts with magmatically derived CO₂ to form CH₄ and higher HCs. However, new petrographic, microthermometric, laser Raman, bulk gas and isotope data are presented and discussed in the context of previously published work in order to reassess models of HC generation. The gas phase is dominated by CH₄ with only minor proportions of higher hydrocarbons. No remnants of the proposed primary CO₂-rich fluid are found in the complex. The majority of the fluid inclusions are of secondary nature and trapped in healed microfractures. This indicates a high fluid flux after magma crystallisation. Entrapment conditions for fluid inclusions are 450–550 °C at 2.8–4.5 kbar. These temperatures are too high for hydrocarbon gas generation through the FT reaction. Chemical analyses of rims of Fe-rich phases suggest that they are not the result of alteration but instead represent changes in magma composition during crystallisation. Furthermore, there is no clear relationship between the presence of Fe-rich minerals and the abundance of fluid inclusion planes (FIPs) as reported elsewhere. δ¹³C values for methane range from − 22.4‰ to − 5.4‰, confirming a largely abiogenic origin for the gas. The presence of primary CH₄-dominated fluid inclusions and melt inclusions, which contain a methane-rich gas phase, indicates a magmatic origin of the HCs. An increase in methane content, together with a decrease in δ¹³C isotope values towards the intrusion margin suggests that magmatically derived abiogenic hydrocarbons may have mixed with biogenic hydrocarbons derived from the surrounding country rocks.     

Methane-bearing,aqueous, saline solutions in the Skaergaard intrusion,east Greenland

Solutions of H₂O–NaCl–CH₄ occur in fluid inclusions enclosed by quartz, apatite and feldspar from gabbroic pegmatitites, anorthositic structures and intercumulus minerals within the Skaergaard intrusion. The majority of the fluid inclusions resemble 10 m diameter sub-to euhedral negative crystals. A vapour phase and a liquid phase are visible at room temperature, solids are normally absent. The salinity of the fluids ranges from 17.5 to 22.8 wt.% NaCl. CH₄, which comprises less than six mole percent of the solution, was detected in the vapour phase of the fluid inclusions with Raman microprobe analysis. Homogenization of the fluid inclusions occurred in the liquid phase in the majority of the fluid inclusions, though 10% of the inclusions homogenized in the gas phase. Thermodynamic consideration of the stability of feldspars + quartz, and the C–O–H system, indicates that the solutions were trapped at temperatures between 655 and 770°C, at oxygen fugacities between 1.5 and 2.0 log units below the QFM oxygen buffer. Textural evidence and the composition of the solutions suggest that the fluids coexisted with late-magmatic intercumulus melts and the melts which formed gabbroic pegmatites. These solutions are thought to have contributed to late-magmatic metasomatism of the primocryst assemblages of the Skaergaard intrusion.     

Fluid inclusions in Scourian granulites from the Lewisian complex of NW Scotland: evidence for CO2-rich fluid in Late Archaean high-grade metamorphism

In this paper the first fluid-inclusion data are presented from Late Archaean Scourian granulites of the Lewisian complex of mainland northwest Scotland. Pure CO₂ or CO₂-dominated fluid inclusions are moderately abundant in pristine granulites. These inclusions show homogenization temperatures ranging from − 54 to + 10 °C with a very prominent histogram peak at − 16 to − 32 °C. Isochores corresponding to this main histogram peak agree with P-T estimates for granulite-facies recrystallization during the Badcallian (750–800 °C, 7–8 kbar) as well as with Inverian P-T conditions (550–600 °C, 5 kbar). The maximum densities encountered could correspond to fluids trapped during an early, higher P-T phase of the Badcallian metamorphism (900–1000 °C, 11–12 kbar). Homogenization temperatures substantially higher than the main histogram peak may represent Laxfordian reworking (≤ 500 °C, < 4 kbar). In the pristine granulites, aqueous fluid inclusions are of very subordinate importance and occur only along late secondary healed fractures. In rocks which have been retrograded to amphibolite facies from Inverian and/or Laxfordian shear zones, CO₂ inclusions are conspicuously absent; only secondary aqueous inclusions are present, presumably related to post-granulite hydration processes. These data illustrate the importance of CO₂-rich fluids for the petrogenesis of Late Archaean granulites, and demonstrate that early fluid inclusions may survive subsequent metamorphic processes as long as no new fluid is introduced into the system.     

Zircon in gabbroids from the axial zone of the Mid-Atlantic ridge, Markov Deep, 6° N: Correlation of geochemical features with petrogenetic processes

This paper reports the results of detailed petrological-geochemical study of zircons and host rocks that were dredged from the Markov Deep area in the slow-spreading Mid-Atlantic ridge. The rocks are represented by variably cataclased gabbronorite with veinlets of oceanic plagiogranite (OPG) as well as leucocratic gabbro (primitive gabbro) and hornblende Fe-Ti oxide gabbronorite (ferrogabbro) without OPG. The studied zircons differ in morphology, inner structure, set of mineral inclusions (ingrowths), and content of trace elements. Compositional heterogeneity is also observed within individual grains. The REE distribution patterns in zircons are characterized by gentle growth from LREE to HREE, with prominent positive Ce anomaly and negative Eu anomaly, and in general fall in the range of zircons from magmatic rocks. Oceanic zircons clearly differ from continental populations in the U/Yb-Y and U/Yb-Hf discrimination diagrams, primarily, due to their lower U/Yb ratio at wide variations of Y and Hf contents. Zircons that contain inclusions of acid glass and hence, crystallized from OPG melt are relatively depleted in REE, especially HREE. This indicates that OPG was formed by partial melting of gabbro in the presence of concentrated water-salt fluid, which extracted REE from the plagiogranite melt. Zircons from gabbroids devoid of OPG inclusions have higher total REE contents than zircons from OPG. Late hydrothermal alterations of zircon are distinctly established by the formation of neogenic collomorphic (porous) texture and/or by composition of mineral inclusions and accompanied by significant enrichment in La. Heterogeneous distribution of Ti in zircon may be caused not only by a change in its crystallization temperature, but also variations in silica to titanium oxide activity ratios in the rocks during interaction with hydrothermal solution of variable acidity. A complex study of structural-morphological and geochemical features of oceanic zircons and phase composition of host rocks and inclusions provides insight into processes leading to the crystallization and subsequent evolution of this mineral in the rocks of oceanic lithosphere.     

Fluid inclusions in chromite from a pyroxenite dike of the Pindos ophiolite complex

Chromitite occurrences in the Pindos ophiolite complex are located in elongated dunite bodies hosted in harzburgite of the mantle sequence, and show a compositional variation from high-Al to high-Cr type. Although the majority of the chromite ores is characterized by paucity in fluid inclusions, abundant fluid inclusions were found in chromite hosted by a coarse-grained pyroxenite dike at the Spanos Valley, Pindos complex. Chromite occurs in highly variable proportion in an orthopyroxene matrix or as inclusions in orthopyroxenes. Its composition is homogeneous and has an average Cr/(Cr+Al) ratio 0.73.The investigation of chromitites revealed the presence of primary and secondary fluid inclusions. The primary inclusions are of following types: Three-phase solid-liquid-gas, three-phase liquid-liquid-gas, two-phase liquid-gas and one-phase octahedron crystal-shaped. The secondary fluid inclusions are two-phase liquid-gas and mono-phase fluid inclusions.The presence of fluid inclusions in chromite aggregates hosted in orthopyroxenite dikes, in combination with the trace element contents in chromite concentrates and the mineralogical composition of the dikes may indicate that an aqueous phase separated from the magma.     

大冶铁矿床夕卡岩矿物中熔融包裹体的发现及其地质地球化学意义

以显微照片方式报道了对大冶铁矿床夕卡岩矿物中熔融包裹体、熔－流包裹体和流体包裹体的观察结果和对包裹体相态特征的研究结果。结果表明,在所研究的包裹体中,矿物熔融包裹体最为常见,偶见熔－流包裹体和流体包裹体。熔融包裹体在大冶铁矿床夕卡岩矿物中不仅存在而且广泛分布,在偏光显微镜下很容易找到。熔融包裹体的存在对夕卡岩传统的接触交代成因观点具有挑战性,有助于夕卡岩和夕卡岩矿床成因理论研究水平的提高。     

Fluid and melt inclusion evidence for the origin of idiomorphic quartz crystals in topaz-bearing granite from the Salmi batholith, Karelia, Russia

Idiomorphic quartz crystals in topaz-bearing granite from the Salmi batholith contain primary inclusions of silicate melt and abundant mostly secondary aqueous fluid inclusions. Microthermometric measurements on melt inclusions give estimates for the granite solidus and liquidus of 640–680°C and 770–830°C, respectively. Using published solubility models for H₂O in granitic melts and the obtained solidus/liquidus temperatures from melt inclusions, the initial water concentration of the magma is deduced to have been approximately 3 wt.% and the minimum pressure about 2 kbar. At this initial stage, volatile-undersaturation conditions of magma were assumed. These results indicate that the idiomorphic quartz crystals are magmatic in origin and thus real phenocrysts. During subsolidus cooling and fracturing of the granite, several generations of aqueous fluid inclusions were trapped into the quartz phenocrysts. The H₂O inclusions have salinities and densities of 1–41 wt.% NaCl eq. and 0.53–1.18 g/cm³, respectively.     

Garnet re‐equilibration by coupled dissolution–reprecipitation: evidence from textural,major element and oxygen isotope zoning of ‘cloudy’ garnet

The analysis of texture, major element and oxygen isotope compositions of cloudy garnet crystals from a metapelite sampled on Ikaria Island (Greece) is used to assess the model of growth and re‐equilibration of these garnet crystals and to reconstruct the pressure–temperature–fluid history of the sample. Garnet crystals show complex textural and chemical zoning. Garnet cores (100–200 μm) are devoid of fluid inclusions. They are characterized by growth zoning demonstrated by a bell‐shaped profile of spessartine component (7–3 mol.%), an increase in grossular from 14 to 22 mol.% and δ¹⁸O values between 9.5 ± 0.3‰ and 10.4 ± 0.2‰. Garnet inner rims (90–130 μm) are fluid inclusion‐rich and show a decreasing grossular component from 22 to 5 mol.%. The trend of the spessartine component observed in the inner rim allows two domains to be distinguished. In contrast to domain I, where the spessartine content shows the same trend as in the core, the spessartine content of domain II increases outwards from 2 to 14 mol.%. The δ¹⁸O values decrease towards the margins of the crystals to a lowest value of 7.4 ± 0.2‰. The outer rims (<10 μm) are devoid of fluid inclusions and have the same chemical composition as the outermost part of domain II of the inner rim. Garnet crystals underwent a four‐stage history. Stage 1: garnet growth during the prograde path in a closed system for oxygen. Garnet cores are remnants of this growth stage. Stage 2: garnet re‐equilibration by coupled dissolution–reprecipitation at the temperature peak (630 < T < 650 °C). This causes the creation of porosity as the coupled dissolution–reprecipitation process allows chemical (Ca) and isotopic (O) exchange between garnet inner rims and the matrix. The formation of the outer rim is related to the closure of porosity. Stage 3: garnet mode decreases during the early retrograde path, but garnet is still a stable phase. The resulting garnet composition is characterized by an increasing Mn content in the inner rim’s domain II caused by intracrystalline diffusion. Stage 4: dissolution of garnet during the late retrograde path as garnet is not a stable phase anymore. This last stage forms corroded garnet. This study shows that coupled dissolution–reprecipitation is a possible re‐equilibration process for garnet in metamorphic rocks and that intra‐mineral porosity is an efficient pathway for chemical and isotopic exchange between garnet and the matrix, even for otherwise slow diffusing elements.     

Fluid inclusions in apatite from Jacupiranga calcite carbonatites: Evidence for a fluid-stratified carbonatite magma chamber

Carbonatites of the Jacupiranga alkaline–carbonatite complex in São Paulo State, Brazil, were used to investigate mineral–fluid interaction in a carbonatite magma chamber because apatite showed a marked discontinuity between primary fluid inclusion-rich cores and fluid inclusion-poor rims. Sylvite and burbankite, apatite, pyrite, chalcopyrite and ilmenite are the common phases occurring as trapped solids within primary fluid inclusions and reflect the general assemblage of the carbonatite. The apatite cores had higher Sr and REE concentrations than apatite rims, due to the presence of fluid inclusions into which these elements partitioned. A positive cerium anomaly was observed in both the core and rim of apatite crystals because oxidised Ce⁴⁺ partitioned into the magma. The combined evidence from apatite chemistry, fluid inclusion distribution and fluid composition was used to test the hypotheses that the limit of fluid inclusion occurrence within apatite crystals arises from: (1) generation of a separate fluid phase; (2) utilization of all available fluid during the first stage of crystallization; (3) removal of crystals from fluid-rich magma to fluid-poor magma; (4) an increase in the growth rate of apatite; or (5) escape of the fluids from the rim of the apatite after crystallization. The findings are consistent with fractionation and crystal settling of a carbonatite assemblage in a fluid-stratified magma chamber. Secondary fluid inclusions were trapped during a hydrothermal event that precipitated an assemblage of anhedral crystals: strontianite, carbocernaite, barytocalcite, barite and norsethite, pyrophanite, magnesian siderite and baddeleyite, ancylite-(Ce), monazite-(Ce) and allanite. The Sr- and REE-rich nature of the secondary assemblage, and lack of a positive cerium anomaly indicate that hydrothermal fluids have a similar source to the primary magma and are related to a later carbonatite intrusion.     

Petrogenetic significance of solid carbonate inclusions in apatite of the Sukulu carbonatite, Uganda

Many solid inclusions occur in apatite of the Sukulu carbonatite, Uganda, of which the most abundant are carbonate, which can be classified into clear (Mg-calcite) and pitted (calcite) inclusions based on their morphology, texture and chemical composition. Although such solid inclusions are ubiquitous in carbonatite apatite and have been described by many workers, this study provides new insight into their genesis and petrogenetic significance.

The pitted inclusions commonly have elongate or spherical shapes and are spatially related to microfractures in the apatite host. They probably developed from early primary aqueous or Mg-calcite solid inclusions by infiltration of post-magmatic fluids through the microfractures. The clear inclusions generally have spheroidal shapes and are thought to represent an early magmatic phase and to be typically magmatic in origin.

Electron microprobe analysis indicates that the clear inclusions contain > 1.6 wt.% MgO and the pitted ones <0.5 wt.% MgO. The FeO content also differs, the clear inclusions containing about twice as much FeO as the pitted ones. Heating experiments suggest that some of the clear inclusions must be representative of crystals precipitated at high temperature ( > 1100°C) prior to apatite formation. In contrast, other clear inclusions became dark or brownish and remarkably homogeneous on heating at relatively moderate temperatures (740–912°C) indicating that they may represent true melt inclusions trapped as melts during apatite growth.

The present findings clearly illustrate the importance of both magmatic and post-magmatic processes in the genesis of the carbonate of the Sukulu carbonatite complex. They also suggest that extensive post-magmatic processes are likely to have been responsible for development of the low Mg-calcite and associated dolomite which dominate the sovites of this complex.