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1.
X‐ray composition maps and quantitative analyses for Mn, Ca and Cr have been made for six pelitic and calc‐pelitic garnet crystals and Al, Fe and Cr analyses maps have been made for two kyanite crystals, from lower and mid/upper amphibolite facies rocks from the Grenville Province of western Labrador, using an electron microprobe analyser and a laser ablation ICP‐MS. Garnet with spiral (‘snowball’) internal fabrics (Si) has spiral zoning in major elements, implying that growth was concentrated in discrete regions of the crystal at any one time (spiral zoning). Cr zoning is parallel to Si in low amphibolite facies garnet with both straight and spiral internal fabrics, indicating that the garnet overprinted a fabric defined by Cr‐rich (mica±chlorite±epidote) and Cr‐poor (quartz±plagioclase) layers during growth (overprint zoning) and that Cr was effectively immobile. In contrast, in mid/upper amphibolite facies garnet porphyroblasts lacking Si, Cr zoning is concentric, implying that Cr diffusion occurred. Cr zoning in kyanite porphyroblasts appears superficially similar to oscillatory zoning, with up to three or four annuli of Cr enrichment and/or depletion present in a single grain. However, the variable width, continuity, Cr concentration and local bifurcation of individual annuli suggest that an origin by overprint zoning may be more likely. The results of this study explain previously observed nonsystematic Cr zoning in garnet and irregular partitioning of Cr between coexisting metamorphic mineral pairs. In addition, this study points to the important role of crystal growth rate in determining the presence or absence of inclusions and the type of zoning exhibited by both major and trace elements. During fast growth, inclusions are preferentially incorporated into the growing porphyroblast and slow diffusing elements such as Cr are effectively immobile, whereas during slow growth, inclusions are not generally included in the porphyroblast and Cr zoning is concentric.  相似文献   

2.
Metamorphic equilibration requires chemical communication between minerals and may be inhibited through sluggish volume diffusion and or slow rates of dissolution in a fluid phase. Relatively slow diffusion and the perceived robust nature of chemical growth zoning may preclude garnet porphyroblasts from readily participating in low‐temperature amphibolite facies metamorphic reactions. Garnet is widely assumed to be a reactant in staurolite‐isograd reactions, and the evidence for this has been assessed in the Late Proterozoic Dalradian pelitic schists of the Scottish Highlands. The 3D imaging of garnet porphyroblasts in staurolite‐bearing schists reveals a good crystal shape and little evidence of marginal dissolution; however, there is also lack of evidence for the involvement of either chlorite or chloritoid in the reaction. Staurolite forms directly adjacent to the garnet, and its nucleation is strongly associated with deformation of the muscovite‐rich fabrics around the porphyroblasts. “Cloudy” fluid inclusion‐rich garnet forms in both marginal and internal parts of the garnet porphyroblast and is linked both to the production of staurolite and to the introduction of abundant quartz inclusions within the garnet. Such cloudy garnet typically has a Mg‐rich, Mn‐poor composition and is interpreted to have formed during a coupled dissolution–reprecipitation process, triggered by a local influx of fluid. All garnet in the muscovite‐bearing schists present in this area is potentially reactive, irrespective of the garnet composition, but very few of the schists contain staurolite. The staurolite‐producing reaction appears to be substantially overstepped during the relatively high‐pressure Barrovian regional metamorphism reflecting the limited permeability of the schists in peak metamorphic conditions. Fluid influx and hence reaction progress appear to be strongly controlled by subtle differences in deformation history. The remaining garnet fails to achieve chemical equilibrium during the reaction creating distinctive patchy compositional zoning. Such zoning in metamorphic garnet created during coupled dissolution–reprecipitation reactions may be difficult to recognize in higher grade pelites due to subsequent diffusive re‐equilibration. Fundamental assumptions about metamorphic processes are questioned by the lack of chemical equilibrium during this reaction and the restricted permeability of the regional metamorphic pelitic schists. In addition, the partial loss of prograde chemical and textural information from the garnet porphyroblasts cautions against their routine use as a reliable monitor of metamorphic history. However, the partial re‐equilibration of the porphyroblasts during coupled dissolution–reprecipitation opens possibilities of mapping reaction progress in garnet as a means of assessing fluid access during peak metamorphic conditions.  相似文献   

3.
Garnet grains from an intensely metasomatized mid‐crustal shear zone in the Reynolds Range, central Australia, exhibit a diverse assortment of textural and compositional characteristics that provide important insights into the geochemical effects of fluid–rock interaction. Electron microprobe X‐ray maps and major element profiles, in situ secondary ion mass spectrometry oxygen isotope analyses, and U–Pb and Sm–Nd geochronology are used to reconstruct their thermal, temporal and fluid evolution. These techniques reveal a detailed sequence of garnet growth, re‐equilibration and dissolution during intracontinental reworking associated with the Ordovician–Carboniferous (450–300 Ma) Alice Springs Orogeny. A euhedral garnet porphyroblast displays bell‐shaped major element profiles diagnostic of prograde growth zoning during shear zone burial. Coexisting granulitic garnet porphyroclasts inherited from precursor wall rocks show extensive cation re‐equilibration assisted by fracturing and fragmentation. Oxygen isotope variations in the former are inversely correlated with the molar proportion of grossular, suggesting that isotopic fractionation is linked to Ca substitution. The latter generally show close correspondence to the isotopic composition of their precursor, indicating slow intergranular diffusion of O relative to Fe2+, Mg and Mn. Peak metamorphism associated with shearing (～550 °C; 5.0–6.5 kbar) occurred at c. 360 Ma, followed by rapid exhumation and cooling. Progressive Mn enrichment in rim domains indicates that the retrograde evolution caused partial garnet dissolution. Accompanying intra‐mineral porosity production then stimulated limited oxygen isotope exchange between relict granulitic garnet grains and adjacent metasomatic biotite, resulting in increased garnet δ18O values over length scales <200 μm. Spatially restricted oxygen interdiffusion was thus facilitated by increased fluid access to reaction interfaces. The concentration of Ca in channelled fracture networks suggests that its mobility was enhanced by a similar mechanism. In contrast, the intergranular diffusion of Fe2+, Mg and Mn was rock‐wide under the same P–T regime, as demonstrated by a lack of local spatial variations in the re‐equilibration of these components. The extraction of detailed reaction histories from garnet must therefore take into account the variable length‐ and time‐scales of elemental and isotopic exchange, particularly where the involvement of a fluid phase enhances the possibility of measureable resetting profiles being generated for slowly diffusing components such as Ca and O, even at low ambient temperatures and relatively fast cooling rates.  相似文献   

4.
Highly variable distributions of yttrium and rare earth elements (Y+REEs) are documented in pelitic garnet from the Picuris Mountains, New Mexico, and from Passo del Sole, Switzerland, and in mafic garnet from the Franciscan Complex, California. The wide variety of these Y+REE zoning patterns, and those described previously in other occurrences, imply diverse origins linked to differing degrees of mobility of these elements through the intergranular medium during garnet growth. In the Picuris Mountains, large, early‐nucleating crystals have radial profiles of Y+REE dominated by central peaks and annular maxima, in patterns that vary systematically with atomic number. Superimposed on these features are narrow spikes in HREEs and MREEs, located progressively rimward with decreasing atomic number. In contrast, profiles in small, late‐nucleating crystals contain only broad central maxima for all Y+REEs. In garnet from Passo del Sole, Y+REE zoning varies radically from sample to sample: in some rocks, crystals of all sizes display only central peaks for all Y+REEs; in others, profiles exhibit irregular fluctuations in Y+REE contents that match up with small‐scale patchy zoning in Y and Ca X‐ray maps. In the Franciscan Complex, Y+REE in garnet cores fluctuate unsystematically, but mantles and rims display concentric oscillatory zoning for both major elements and Y+REEs. Our interpretation of the complexity of Y+REE distributions in metamorphic garnet centres on the concept that these distributions vary primarily in response to the length scales over which these elements can equilibrate during garnet growth. Very short length scales of equilibration, due to low intergranular mobility, produce overprint zoning characterized by small‐scale irregularities. Higher but still restricted mobility yields diffusion‐controlled uptake, characterized by patterns of central peaks and annular maxima that vary with atomic number and are strongly influenced by T–t paths during garnet growth. Still greater mobility permits progressively greater, potentially rock‐wide, equilibration with major‐ and accessory‐phase assemblages, leading to mineralogical controls: an unchanging mineral assemblage during garnet growth produces bell‐shaped profiles resembling those produced by Rayleigh fractionation, whereas changes in major‐ and/or accessory‐phase assemblages produce profiles with distinct annuli and sharp discontinuities in concentration. The very high mobility associated with influxes of Y+REE‐bearing fluids can cause these element distributions to be dominated by factors external to the rock, yielding profiles characterized by abrupt shifts or oscillations that are not correlated to changes in mineral assemblages.  相似文献   

5.
Disequilibrium for Ca during growth of pelitic garnet   总被引：14，自引：1，他引：14  
Compositional zoning in hundreds of almandine-rich garnets in amphibolite by facies micaceous quartzites from the Picuris Range, north-central New Mexico USA, indicates that although Mn, Mg and Fe achieve chemical equilibrium at hand-sample scale during garnet growth, Ca does not. Instead, Ca concentrations at the surface of growing garnets appear to depend strongly on kinetic factors that govern the local chemical environment, yielding disequilibrium for Ca at scales larger than the region immediately surrounding an individual porphyroblast. Detailed zoning profiles were obtained for 371 garnet crystals in a small volume of a single sample of garnetiferous quartzite, and core analyses were made of 97 additional crystals. Each analysis was made on a section that passed precisely through the morphological centre of the crystal, located by means of 3-D imagery from computed X-ray tomography. The data reveal strong correlations between crystal size and concentrations of Mn, Mg and Fe (but not Ca) in garnet cores; a relationship between crystal size and isolation; rigorous cross-correlations among concentrations of Mn, Mg and Fe (but not Ca); and systematic variations in Ca concentrations as a function of crystal size and core composition that are anomalous in comparison to the behaviour of the other divalent cations. We interpret these observations as the result of thermally accelerated diffusion-controlled garnet growth, in circumstances that promoted rapid intergranular diffusion and thus rock-wide equilibration of Mn, Mg and Fe, but that prevented equilibration at similar scale for Ca because of its more sluggish intergranular diffusion. The anomalous behaviour of Ca is made evident in these garnets by the presence of sharp spikes in Ca concentration, which are demonstrably not a consequence of any simultaneous rock-wide event, such as a change in pressure, temperature, or some other intensive parameter. Instead, Ca concentrations probably reflect the local extent of reaction in the immediate vicinity of each porphyroblast. To the degree that such kinetic factors introduce departures from chemical equilibrium for Ca, thermobarometric estimates that involve grossular contents of pelitic garnet will be in error.  相似文献   

6.
A detailed analysis of chemical zoning in two garnet crystals from Harpswell Neck, Maine, forms the basis of an interpretation of garnet nucleation and growth mechanisms. Garnet apparently nucleates initially on crenulations of mica and chlorite and quickly overgrows the entire crenulation, giving rise to complex two‐dimensional zoning patterns depending on the orientation of the thin section cut. Contours of Ca zoning cross those of Mn, Fe and Mg, indicating a lack of equilibrium among these major garnet constituents. Zoning of Fe, Mg and Mn is interpreted to reflect equilibrium with the rock matrix, whereas Ca zoning is interpreted to be controlled by diffusive transport between the matrix and the growing crystal. Image analysis reveals that the growth of garnet is more rapid along triple‐grain intersections than along double‐grain boundaries. Moreover, different minerals are replaced by garnet at different rates. The relative rate of replacement by garnet along double‐grain boundaries is ordered as muscovite > chlorite > plagioclase > quartz. Flux calculations reveal that replacement is limited by diffusion of Si along double‐grain boundaries to or from the local reaction site. It is concluded that multiple diffusive pathways control the bulk replacement of the rock matrix by garnet, with Si and Al transport being rate limiting in these samples.  相似文献   

7.
Static heating during intrusion of the Makhavinekh Lake Pluton (MLP) caused replacement of garnet in the adjacent country rocks (Tasiuyak Gneiss) by coronal assemblages of orthopyroxene + cordierite. Thermometry based on Al solubility in orthopyroxene, applied to relict garnet and neighbouring orthopyroxene, preserves a temperature gradient from 700 to 900 °C at distances between 5750 and 20 m from the intrusion, reaffirming the robustness of this thermometry technique. Intracrystalline and intergranular variations of Al zoning in orthopyroxene are well‐preserved, suggesting that little diffusional modification of Al growth zoning occurred. Maximum Al2O3 in orthopyroxene ranges from c. 2.0 wt% at 5750 m from the intrusion to a maximum of 4.3 wt% at the contact. Individual orthopyroxene grains show decreasing Al from core to rim in samples < 500 m from the intrusion, while those at greater distances show an increase from core to rim. These features are interpreted with the aid of numerical models for conductive heat flow in the aureole. Coronas in samples close to the intrusion grew at high temperatures and along T‐t paths dominated by cooling, so maximum Al content in orthopyroxene in these samples occurs in the cores of grains that grew during the earliest stages of garnet consumption. In contrast, the corona‐forming reactions in rocks further from the contact proceeded along prograde heating paths, so maximum Al content in orthopyroxene occurs in the rims of grains that grew during the final stages of garnet consumption. These results document the ability of Al‐in‐orthopyroxene thermometry to preserve a detailed record of thermal histories in contact‐metamorphic granulites; they suggest that similar intracrystalline and intergranular variations of Al zoning in orthopyroxene in regional granulites may also preserve portions of both the prograde and peak‐T evolution.  相似文献   

8.
A new discovery of lawsonite eclogite is presented from the Lancône glaucophanites within the Schistes Lustrés nappe at Défilé du Lancône in Alpine Corsica. The fine‐grained eclogitized pillow lava and inter‐pillow matrix are extremely fresh, showing very little evidence of retrograde alteration. Peak assemblages in both the massive pillows and weakly foliated inter‐pillow matrix consist of zoned idiomorphic Mg‐poor (<0.8 wt% MgO) garnet + omphacite + lawsonite + chlorite + titanite. A local overprint by the lower grade assemblage glaucophane + albite with partial resorption of omphacite and garnet is locally observed. Garnet porphyroblasts in the massive pillows are Mn rich, and show a regular prograde growth‐type zoning with a Mn‐rich core. In the inter‐pillow matrix garnet is less manganiferous, and shows a mutual variation in Ca and Fe with Fe enrichment toward the rim. Some garnet from this rock type shows complex zoning patterns indicating a coalescence of several smaller crystallites. Matrix omphacite in both rock types is zoned with a rimward increase in XJd, locally with cores of relict augite. Numerous inclusions of clinopyroxene, lawsonite, chlorite and titanite are encapsulated within garnet in both rock types, and albite, quartz and hornblende are also found included in garnet from the inter‐pillow matrix. Inclusions of clinopyroxene commonly have augitic cores and omphacitic rims. The inter‐pillow matrix contains cross‐cutting omphacite‐rich veinlets with zoned omphacite, Si‐rich phengite (Si = 3.54 apfu), ferroglaucophane, actinolite and hematite. These veinlets are seen fracturing idiomorphic garnet, apparently without any secondary effects. Pseudosections of matrix compositions for the massive pillows, the inter‐pillow matrix and the cross‐cutting veinlets indicate similar P–T conditions with maximum pressures of 1.9–2.6 GPa at temperatures of 335–420 °C. The inclusion suite found in garnet from the inter‐pillow matrix apparently formed at pressures below 0.6–0.7 GPa. Retrogression during initial decompression of the studied rocks is only very local. Late veinlets of albite + glaucophane, without breakdown of lawsonite, indicate that the rocks remained in a cold environment during exhumation, resulting in a hairpin‐shaped P–T path.  相似文献   

9.
The growth history of two populations of snowball garnet from the Lukmanier Pass area (central Swiss Alps) was examined through a detailed analysis of three-dimensional geometry, chemical zoning and crystallographic orientation. The first population, collected in the hinge of a chevron-type fold, shows an apparent rotation of 360°. The first 270° are characterized by spiral-shaped inclusion trails, gradual and concentric Mn zoning and a single crystallographic orientation, whereas in the last 90°, crenulated inclusion trails and secondary Mn maxima centred on distinct crystallographic garnet domains are observed. Microstructural, geochemical and textural data indicate a radical change in growth regime between the two growth sequences. In the first 270°, growth occurred under rotational non-coaxial flow, whereas in the last 90°, garnet grew under a non-rotational shortening regime. The second population, collected in the limb of the same chevron-type fold structure, is characterized by a spiral geometry that does not exceed 270° of apparent rotation. These garnet microstructures do not record any evidence for a modification of the stress field during garnet growth. Concentric Mn zoning as well as a single crystallographic orientation are observed for the entire spiral. Electron backscatter diffraction data indicate that nearly all central domains in the snowball garnet are characterized by one [001] axis oriented (sub-)parallel to the symmetry axis and by another [001] axis oriented (sub-)parallel to the orientation of the internal foliation. These features suggest that the crystallographic orientation across the garnet spiral is not random and that a relation exists among the symmetry axis, the internal foliation and the crystallographic orientation.  相似文献   

10.
The relative timing of two discrete pulses of metamorphic fluid flow is constrained based on chemical zoning in several garnet crystals from Kvaløya, Troms, northern Norway. The garnet crystals measured 1–2 cm in diameter and were contained within c. 1.6 Ga, staurolite grade metasediments. Major element zoning indicates that garnet grew under normal prograde conditions in the garnet and/or staurolite zones. Timing constraints are based on comparisons between major and trace element chemical zoning, oxygen isotope (δ18O) zoning and deformational (inclusion trail) zoning in one of the garnet. We interpret at least two pulses of metamorphic fluid flow. The first pulse occurred during the syn‐tectonic growth interval. The δ18O zoning was reversed relative to ‘normal’ prograde zoning and the δ18O maximum was located within the syn‐tectonic growth zone, displaced 3–4 mm from the garnet core. The fluid might have been sourced in neighbouring calcareous pelites and may also have caused formation of an Y ring. The second (and subsequent) pulse(s) occurred during/after the post‐tectonic growth interval. δ18O was locally increased at the garnet rim, particularly where the rim was sheared. The incomplete rim was also enriched in calcium. Transport of oxygen and calcium by metamorphic fluids is well documented. Transport of Y is both problematic and poorly understood, but might have been facilitated by complexing with F and/or CO2.  相似文献   

11.
It is generally thought that garnet in metapelites is produced by continuous reactions involving chlorite or chloritoid. Recent publications have suggested that the equilibrium temperatures of garnet‐in reactions may be significantly overstepped in regionally metamorphosed terranes. The growth of small spessartine–almandine garnet crystals on Mn‐siderite at the garnet isograd in graphitic metapelites in the Proterozoic Black Hills orogen, South Dakota, demonstrates that Mn‐siderite was the principal reactant that produced the initial garnet in the schists. Moreover, the positions of garnet compositions in isobaric, T–(C/H) pseudosections for the schists show that the temperature of the garnet‐in reaction from Mn‐siderite was overstepped minimally at the most. In the Black Hills, garnet was initially produced during regional metamorphism beginning at c. 1755 Ma due to the collision of Wyoming and Superior cratons, and was subsequently partially or fully re‐equilibrated at more elevated temperatures and pressures during intrusion of the Harney Peak Granite (HPG) at c. 1715 Ma. Garnet occurs in graphitic schists in garnet, staurolite and sillimanite zones, the latter being a product of contact metamorphism by HPG. During metamorphism, coexisting fluid contained both CO2 and CH4. In the garnet zone, garnet crystals contain petrographically distinct cores with inclusions of quartz, graphite and other minerals. Centres of the cores have distinctly elevated Y concentrations that mark the positions of garnet nucleation. The elevated Y is thought to have come from the Mn‐siderite onto which Y was probably absorbed during precipitation in an ocean. In the upper garnet and staurolite zones, the cores were overgrown by inclusion‐poor mantles. Mantles are highly zoned and have more elevated Fe and Mg and lower Mn and Ca than cores. The growth of mantles is attributed to late‐orogenic heating by leucogranite magmas and attendant influx of H2O that caused consumption of graphite in rock matrices. A portion of the Proterozoic terrane that includes the HPG is surrounded by four large faults. In this ‘HPG block’, garnet is inclusion‐poor and its composition does not preserve its early growth history. This garnet appears to have re‐equilibrated by internal diffusion of its major components and/or recrystallization of an earlier inclusion‐rich garnet. It has equilibrated within the kyanite stability range, and together with remnant kyanite in the high‐strain aureole of the HPG, indicates that the HPG block had a ≥6 kbar history. The HPG block has undergone decompression during emplacement of the HPG. The decompression is evident in occurrences of retrograde andalusite and cordierite in the thermal aureole of the HPG. The data support a polybaric metamorphic history of the Black Hills orogen with different segments of the orogen having their own clockwise P–T–t paths.  相似文献   

12.
During prograde metamorphism garnet and, in some higher grade samples, staurolite were produced in a chlorite-chloritoid schist, part of the Precambrian Z to Cambrian Hoosac Formation near Jamaica, VT. Garnet grew during two prograde events separated by a retrogression. This sequence resulted in distinctive inclusion textures and zoning anomalies in garnet produced by diffusive alteration. Textures, reaction space analysis, and mineral compositional variations constrain the possible sequence of reactions in these rocks. Below the staurolite isograd, and to some unknown extent above it, garnet grew by the reaction chloritoid+chlorite+quartz→garnet+H2O. With increasing grade the mineral compositions are displaced towards lower Mn/Fe and higher Mg/Fe ratios. The data are compatible with equilibrium with respect to exchange reactions for the matrix assemblages on a thin section scale and with minerals having closely followed equilibrium paths during reaction. The staurolite isograd coincides with the reaction chloritoid+quartz→garnet+staurolite+chlorite+H2O. This reaction is continuous and trivariant with ZnO becoming an additional component concentrated in staurolite. During this reaction both the Mn/Fe and Mg/Fe ratios of the phases appear to have decreased. This new chemical trend is recorded by garnet zoning profiles and is compatible with trends predicted from phase diagrams. Thus there are two distinct types of garnet zoning reversals in these samples. One is near the textural unconformity and is best explained by diffusive alteration during partial resorption of first stage garnet. The other occurs near the outer rim of garnet in staurolite zone samples and marks the onset of a new prograde garnet producing reaction.  相似文献   

13.
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.  相似文献   

14.
Quantitative strain rates at outcrop scale are very difficult to obtain, but they may be estimated from crystals with curved inclusion trails by calculating rotation rates from growth rates and corresponding deflections of the internal foliation. Garnet in a quartzose pelite at Passo del Sole in the central Swiss Alps is extraordinarily valuable for calculation of strain rates during Alpine orogenesis, because the unusual zoning patterns clearly define the kinetics of its nucleation and growth. Complex concentric zoning patterns can be correlated from one crystal to another in a hand sample, based on compositional and microstructural similarities; the ubiquity of these features demonstrates that all garnet crystals nucleated at nearly the same time. Compositional bands whose radial widths are proportional to crystal size provide evidence for growth governed by the kinetics of intergranular diffusion of locally sourced nutrients. Together, these constraints increase the reliability of estimates of rates of garnet growth, and the strain‐rate calculations that depend on them. To obtain growth rates, P–T conditions during garnet crystallization were modelled in a series of pseudosections, and compositional evolution was connected to rates of garnet growth by means of an independently determined heating rate. These growth rates, combined with measured amounts of curvature of inclusion trails, indicate that the time‐averaged strain rate at Passo del Sole during Alpine metamorphism was on the order of 10?14 s?1. Strain rates calculated using rotational v. non‐rotational models are similar in magnitude. The constraints on crystallization kinetics also allow direct calculation of strain rates during individual stages of garnet growth, revealing short‐term increases to values on the order of 10?13 s?1. These higher strain rates are correlated with the growth of concentric high‐Ca or high‐Mn zones in garnet, which implies that strain softening associated with the transient passage of fluids is responsible for acceleration of deformation during these intervals.  相似文献   

15.
A combined study of major and trace elements, fluid inclusions and oxygen isotopes has been carried out on garnet pyroxenite from the Raobazhai complex in the North Dabie Terrane (NDT). Well‐preserved compositional zoning with Na decreasing and Ca and Mg increasing from the core to rim of pyroxene in the garnet pyroxenite indicates eclogite facies metamorphism at the peak metamorphic stage and subsequent granulite facies metamorphism during uplift. A P–T path with substantial heating (from c. 750 to 900 °C) after the maximum pressure reveals a different uplift history compared with most other eclogites in the South Dabie Terrane (SDT). Fluid inclusion data can be correlated with the metamorphic grade: the fluid regime during the peak metamorphism (eclogite facies) was dominated by N2‐bearing NaCl‐rich solutions, whereas it changed into CO2‐dominated fluids during the granulite facies retrograde metamorphism. At a late retrograde metamorphic stage, probably after amphibolite facies metamorphism, some external low‐salinity fluids were involved. In situ UV‐laser oxygen isotope analysis was undertaken on a 7 mm garnet, and impure pyroxene, amphibole and plagioclase. The nearly homogeneous oxygen isotopic composition (δ18OVSMOW = c. 6.7‰) in the garnet porphyroblast indicates closed fluid system conditions during garnet growth. However, isotopic fractionations between retrograde phases (amphibole and plagioclase) and garnet show an oxygen isotopic disequilibrium, indicating retrograde fluid–rock interactions. Unusual MORB‐like rare earth element (REE) patterns for whole rock of the garnet pyroxenite contrast with most ultra‐high‐pressure (UHP) eclogites in the Dabie‐Sulu area. However, the age‐corrected initial εNd(t) is ? 2.9, which indicates that the protolith of the garnet pyroxenite was derived from an enriched mantle rather than from a MORB source. Combined with the present data of oxygen isotopic compositions and the characteristic N2 content in the fluid inclusions, we suggest that the protolith of the garnet pyroxenite from Raobazhai formed in an enriched mantle fragment, which has been exposed to the surface prior to the Triassic metamorphism.  相似文献   

16.
Abstract An analytical electron microscope study of almandine garnet from a metamorphosed Al–Fe‐rich rock revealed detailed composition profiles and defect microstructures of resorption zoning along fluid‐infiltrated veins and even into the garnet/ilmenite (inclusion) interface. This indicates a limited volume diffusion for the cations in substitution (mainly Ca and Fe) and an interface‐controlled partition for the extension of a composition‐invariant margin. A corrugated interface between the Ca‐rich margin/zone and the almandine garnet core is characterized by dislocation arrays and recovery texture further suggesting a resorption process facilitated by diffusion‐induced recrystallization, diffusion‐induced dislocation migration and diffusion–induced grain boundary migration. Integrated microstructural and chemical studies are essential for understanding the underlying mechanisms of processes such as garnet zoning and its modification. Without this understanding, it will not be possible to reliably use garnet compositions for thermobarometry and other applications that rely on garnet chemical information.  相似文献   

17.
This study presents Lu–Hf geochronology of zoned garnet in high‐P eclogites from the North Qilian orogenic belt. Selected samples have ~mm‐sized garnet grains that have been sampled with a micro‐drill and analysed for dating. The Lu–Hf dates of bulk garnet separates, micro‐drilled garnet cores and the remnant, rim‐enriched garnet were determined by two‐point isochrons, with cores being consistently older than the bulk‐ and rim‐enriched garnet. The bulk garnet separates of each sample define identical garnet–whole rock isochron date of c. 457 Ma. Consistent U–Pb zircon dates of 455 ± 8 Ma were obtained from the eclogite. The Lu–Hf dates of the drilled cores and rim‐rich separates suggest a minimum garnet growth interval of 468.9 ± 2.4 and 452.1 ± 1.6 Ma. Major and Lu element profiles in the majority of garnet grains show well‐preserved Rayleigh‐style fractionated bell‐shaped Mn and Lu zoning profiles, and increasing Mg from core to rim. Pseudosection modelling indicates that garnet grew along a P–T path from ~470–525°C and ~2.4–2.6 GPa. The exceptional high‐Mn garnet core in one sample indicates an early growth during epidote–blueschist facies metamorphism at <460°C and <0.8 GPa. Therefore, the Lu–Hf dates of drilled cores record the early prograde garnet growth, whereas the Lu–Hf dates of rim‐rich fractions provide a maximum age for the end of garnet growth. The microsampling approach applied in this study can be broadly used in garnet‐bearing rocks, even those without extremely large garnet crystals, in an attempt to retrieve the early metamorphic timing recorded in older garnet cores. Given a proper selection of the drill bit size and a detailed crystal size distribution analysis, the cores of the mm‐sized garnet in most metamorphic rocks can be dated to yield critical constraints on the early timing of metamorphism. This study provides new crucial constraints on the timing of the initial subduction (before c. 469 Ma) and the ultimate closure (earlier than c. 452 Ma) of the fossil Qilian oceanic basin.  相似文献   

18.
Quantitative constraints on the accelerative effects of H2O on the kinetics of metamorphic reactions arise from a comparison of rates of intergranular diffusion of Al in natural systems that are fluid‐saturated, hydrous but fluid‐undersaturated, and nearly anhydrous. Widths of symplectitic reaction coronas around partially resorbed garnet crystals in the contact aureole of the Makhavinekh Lake Pluton, northern Labrador, combined with time–temperature histories from conductive thermal models, yield intergranular diffusivities for Al from ～700–900 °C under nearly anhydrous conditions. Those rates, when extrapolated down temperature, are approximately three orders of magnitude slower than rates derived from re‐analysis of garnet resorption coronas formed under hydrous but fluid‐undersaturated conditions near 575 °C in rocks of the Llano Uplift of central Texas, which are in turn approximately four orders of magnitude slower than rates at comparable temperatures derived from numerical simulations of prograde garnet growth in fluid‐saturated conditions in rocks from the Picuris Range of north‐central New Mexico. Thus, even at constant temperature, rates of intergranular diffusion of Al – and corresponding length scales and timescales of metamorphic reaction and equilibration – may vary by as much as seven orders of magnitude across the range of H2O activities found in nature.  相似文献   

19.
Metapelitic residual enclaves in the Neogene Volcanic Province of SE Spain are residues left after melt extraction. Glass (quenched melt) of granitic composition occurs as inclusions in most minerals and as intergranular pockets. The most common enclave types show one stage of garnet growth that is interpreted to have occurred at the same time as glass production. Some of these show a well‐developed foliation outlined by fibrolite, biotite, graphite and glass, which wraps around elongate garnet crystals that have aspect ratios up to 10:1. Based on microstructures and chemistry, the garnet within these rocks shows clear core and mantle structure. The core has an average composition of Alm76–Prp08–Sps14–Grs03 and contains primary inclusions of biotite and melt, trapped during garnet growth. A thin (c. 100 μm), irregular mantle overgrows the garnet core, enclosing oriented fibrolite inclusions in strain caps, and biotite in strain shadows. In places, the overgrowths form skeletal elongated arms, which extend parallel to the foliation. The garnet mantle contains less Mn and higher XMg, but both core and mantle display flat Mn profiles, the contact being a sharp break. Ternary feldspar and Grt–Bt thermometry yield temperatures in the range 800–900 °C, with no systematic differences among the different microstructural domains of elliptical garnet. Based on the observed intracrystalline microstructures, the high amount of melt extraction in the rock by flattening component strain and the chemical zoning of garnet, the formation of elliptical garnet is modelled by a multistage sequence. This involves pressure solution and reprecipitation of the core, followed by post‐kinematic, partly mimetic growth of the garnet mantle.  相似文献   

20.
An analytical study to evaluate quantitatively weak zoning of a garnet from a high-grade kinzigite has been performed with an electron microprobe. The technique consists of the reconstruction of a profile step-by-step by successive analyses performed during relatively long counting times (30 s), along a radial profile of 2,500 μm length. The successive analytical data along this profile are statistically treated by Fisher's test and compared with the χ2 values (Pearson's law). These statistical tests were applied to assess microprobe stability and analysis homogeneity, and as a consequence to assure high credibility of the radial variations of the garnet. From core to rim, and for each element, zoning appears as the radial juxtaposition of stationary Poissonian samples. These samples being associated, the garnet appears to be constituted of successive concentric domains with stationary compositions. Different substitutions between Mg, Fe, Mn and Ca are evidenced. Such an analytical approach to chemical zoning can be useful for understanding growth mechanisms, and the possible diffusion reactions with the environment at each growth step. In addition, such a procedure can be used to evaluate accurately the fluid content of cordierite, and to appreciate the nature of the fluids concerned. As an example, the fluid content of a cordierite from a similar high-grade kinzigite has been evaluated.  相似文献   

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