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1.
Garnet peridotites from the southern Su‐Lu ultra‐high‐pressure metamorphic (UHPM) terrane, eastern China, contain porphyroblastic garnet with aligned inclusions comprising a low‐P–T mineral assemblage (chlorite, hornblende, Na‐gedrite, Na‐phlogopite, talc, spinel and pyrite). Orthopyroxene porphyroblasts show fine exsolution lamellae of clinopyroxene and minor chromite. A clinopyroxene inclusion in garnet shows some orthopyroxene exsolution lamellae. Both the rims of porphyroblastic pyroxene and garnet and the matrix pyroxene and garnet crystallized at the expense of olivine. This is interpreted as a result of metasomatism of the peridotites by an SiO2‐rich melt at UHP conditions. A chromian garnet further overgrew on the rims of the garnet. The XMg values (Mg/(Mg+Fe)) of porphyroblastic garnet decrease from core to rim and vary in different peridotite samples, while the compositions of both the porphyroblastic and the matrix pyroxene are similar in terms of Ca–Mg–Fe. The Mg‐rich cores of porphyroblastic garnet and orthopyroxene record high temperatures and pressures (c. 1000 °C, ≥5.1 GPa), whereas the matrix minerals, including the rims of porphyroblasts, record much lower P–T (c. 4.2 GPa, c. 760 °C). Sm–Nd data give apparent isochron ages of c. 380 Ma and negative εNd(0) values (c.?9). These dates are considered meaningless due to isotopic disequilibrium between garnet cores and the rest of the rocks. The isotopic disequilibrium was probably caused by metasomatism of the peridotites by melt/fluids derived from the coevally subducted crustal materials. On the other hand, the Rb–Sr isotopic systems of phlogopite and clinopyroxene appear to have reached equilibrium and record a cooling age of c. 205 Ma. It is suggested that the garnet peridotites were originally emplaced into a low‐P–T environment prior to the c. 220 Ma continental collision, during which they were subducted together with crustal rocks to mantle depth and subjected to UHP metamorphism. An important corollary is that at least some of the coevally subducted crustal rocks in the Su‐Lu terrane have been subjected to peak metamorphism at P–T conditions much higher than presently estimated (≥2.7 GPa, ≤800 °C).  相似文献   

2.
In the Western Gneiss Region of Norway are found numerous peridotite lenses which have been extensively recrystallized under amphibolite fades conditions during the Caledonian Orogeny. However, evidence for an earlier Caledonian high-pressure metamorphism has been recorded by abundant eclogite and granulite relicts within gneiss and by the presence of at least ten garnet perioditite bodies preserved within chlorite peridotites. Two garnet-bearing ultramafic assemblages have been recognized: olivine-orthopyroxene-clinopyroxene-garnet and olivine-ortho-pyroxene-pargasitic-amphibole-garnet.Except for olivine, minerals in the garnet peridotites are compositionally zoned, with relatively uniform cores and compositional gradients generally confined to the outer 200 micrometers, or less, of grains. The most common zoning patterns at grain margins are an increase in Fe/Mg in garnet, an increase in Al2O3 in orthopyroxene, and a decrease in Na2O and Al2O3 in clinopyroxene, although there are exceptions to these patterns at two localities. These zoning patterns have developed mainly in response to cooling and decompression of the garnet peridotites.Application of geothermometers and barometers to the garnet peridotites has yielded temperatures of 770–860° C and pressures of 30–43 kb for cores of grains and consistently lower temperatures and pressures for rims, except for peridotites on Oterøy, where there is an apparent temperature increase from cores to rims.The petrologic and geothermobarometric evidence for most of the investigated garnet peridotites is compatible with their tectonic emplacement from the upper mantle into thickened continental crust during Caledonian collision of the Baltic and Greenland plates.  相似文献   

3.
ABSTRACT Ion probe traverses across garnets from peridotites of the Caledonides of Norway and the Variscides of Poland show zoning patterns for Y, V, Zr, Cr, Ti and the REE. The complexly zoned patterns of garnets from the Bystrzyca Górna peridotite, Poland, are interpreted in terms of a changing P–T history (isobaric cooling followed by decompression and cooling). Weak rimward gradients in REE concentrations in garnets from the Almklovdalen and Sandvika peridotites, Norway, may be relicts of the original growth history of the garnets, but the nearly flat Y, V, Zr, Cr and Ti profiles from the same garnets imply a later period of near-homogenization at uniform P–T. Crushed garnet separates from each body were separated into three or more fractions on the assumption that density and magnetic susceptibility vary with Fe/Mg ratio, and Fe/Mg ratios change from garnet core to rim. Sm-Nd garnet–clinopyroxene ‘ages’ were determined for each fraction to determine whether they are also zoned. Four garnet fractions from the Góry Sowie peridotite give nearly the same ages (397–412 Ma) that are believed to span the interval of garnet growth. Garnet fractions from the Norwegian peridotites define scattered ages (816–1350 Ma) that are suspect, but hint at a Sveconorwegian equilibration event. The data indicate the Variscan and Norwegian peridotites had different histories, despite superficial mineralogical and tectonic similarities. Norwegian garnet peridotites had a long pre-Caledonian history and were extracted from a relatively cold mantle whereas the Variscan garnet peridotites had a comparatively short pre- or Eo-Variscan history and were extracted from a hot mantle.  相似文献   

4.
Eclogite inclusions from kimberlitic diatremes on the Colorado Plateau contain intricately zoned garnet and pyroxene and unusual textures. Detailed electron microprobe traverses for a clinopyroxene-garnet-phengite-lawsonite-rutile assemblage show garnet zoning from Alm69Gr21Py10 (core) to Alm61Gr13Py26 (rim) and pyroxene zoning from Jd50 (core) through Jd77 to Jd55 (rim). Pyroxene cores are Cr-rich in another rock. Sharp compositional discontinuities and zoning reversals are preserved in garnet and pyroxene. Oscillatory zoning occurs in both phases on a 10–20 m scale, with variations of up to 6% Py in garnet and 15% Jd in pyroxene. Phengite is unzoned and contains 74% celadonite endmember.Skeletal, pyroxene-filled garnet crystals are common in some rocks, and garnets in other rocks clearly began growth as shell-like crystals. Some rocks contain domains of coarse, prismatic pyroxene with very fine-grained, interstitial magnesium silicates. The texture appears to have resulted from crystallization in the presence of a fluid phase, and water pressure is inferred to have equalled total pressure during crystallization. Eclogite formation at high water pressure may reflect subcrustal crystallization.An analysis of error propagation shows that ferrous iron calculations from electron probe data are not meaningful for these jadeitic pyroxenes, and temperature differences between core and rim crystallization cannot be documented. The garnet textures and oscillatory zoning are unusual for metamorphic rocks, and they suggest disequilibrium crystallization after overstepping of reaction boundaries. All data fit a model of eclogite formation during cooling and metasomatism of basaltic dikes intruded into a cool upper mantle, but the results here do not preclude other origins, such as subduction zone metamorphism.  相似文献   

5.
The chemical composition of the pyroxenes and olivines of 12 basaltic rocks and 5 lherzolite nodules was determined quantitatively by electron micro-probe analysis. The composition of the pyroxenes depends on the type of basalt in which they occur. Tholeiitic basalts with normative quartz contain three pyroxenes: orthorombic pyroxenes, pigeonites and augites. All pyroxene phases are zoned and do not show any exsolution. Their Ti and Al contents (Ca-Tschermaks and Ti-augite molecules) are small. All pyroxene phases were formed under disequilibrium with each other and with the melt because of rapid quenching. The sequence of crystallization: orthopyroxene—pigeonite—augite could be established by their Cr content.The alkali olivine basalts undersatured in SiO2 and the olivine nephelinites are characterized by Ti and Al-rich clinopyroxenes. The distribution of Ti and Al in the pyroxenes of the alkali olivine basalts shows a differentiation trend from the cores of the phenocrysts to their outer zones and to the crystals of the ground mass. Thereby the Ca-Tschermaks molecule is being replaced more and more by the Ti-augite molecule. The Ti content of the pyroxenes of the olivine nephelinites decreases in the last stage of differentiation because simultaneously increasing amounts of titaniferous magnetite crystallize.The pyroxenes of lherzolite peridotite nodules are characterized by high Al and low Ti contents which differ according to the type of basalt (alkali olivine basalt or olivine nephelinite) in which the nodules occur. The homogeneous distribution of the elements within the single grains indicates crystallization under equlibrium conditions. The conditions of their formation are comparable to those of Al-pyroxene peridotites in the upper mantle. The composition of pyroxenes of early accumulates of alkali basaltic melts differ from those of peridotite nodules. Therefore lherzolite nodules can be taken as residues of deeper peridotite masses.  相似文献   

6.
Garnet Iherzolite and megacrystalline nodules from The Thumbcomprise the deepest mantle sample recovered from the diatremesand intrusions of the Four Corners area. Discrepancies betweenvarious geothermometers applied to these nodules are believedto reflect zoning of Fe in garnets as well as problems in calibrationof the geothermometers. Because the pyroxenes are not zoned,the pyroxene solvus method probably provides more reliable temperatureestimates for this nodule suite than methods based on partitioningof Fe and Mg with garnet. The preferred T-P range of the nodules,950–1230 °C and 32–40 kb, is thought to reflecta localized perturbation of the ambient geotherm by a diapiricor igneous intrusion. Garnet Iherzolites with coarse texture show a trend from fertileto refractory compositions consistent with variable depletionby partial melting. These nodules are interpreted as previouslydepleted mantle rocks, most of which were relatively littleaffected by the thermal perturbation. Garnet Iherzolites withsheared texture are enriched in Fe and Ti relative to the coarseIherzolites and are suggested to have formed by deformationand metasomatism of the coarse lherzolites during intrusionof magma related to the thermal perturbation. The texturallydiverse ‘megacrystalline’ nodules are interpretedas precipitates from this liquid. They are similar to discretenodules from kimberlite pipes, but have unique characteristicsof their own. The above relationships are thought to recordthe process of deep-seated intrusion and partial crystallizationof evolved liquids, possibly related to the host lamprophyre,shortly before the time of eruption.  相似文献   

7.
Peridotite xenoliths from the Pello tuff cone in the Rift Valley of northern Tanzania, bear witness to upper mantle veining and metasomatism. Veins of katungite composition, with an asthenospheric signature, have imposed K, Fe, Ti, OH and REE metasomatism upon previously depleted peridotite. Chemical and mineralogical gradients are present in the peridotite wall rocks, and hydrous phases developed in the peridotite are generally lower in Ti and Fe, but higher in Mg and Cr, than those in the veins. The metasomatism has reduced the density of affected peridotite by up to 4.5%, supporting earlier geophysical models for low-density mantle beneath the Rift Valley. Age constraints for the metasomatically-induced density decrease permit correlation with Recent faulting in the Rift Valley, but not with the major upwarp of the Kenya Dome in the late Tertiary.  相似文献   

8.
We present petrography and mineral chemistry for both phlogopite,from mantle-derived xenoliths(garnet peridotite,eclogite and clinopyroxene-phlogopite rocks)and for megacryst,macrocryst and groundmass flakes from the Grib kimberlite in the Arkhangelsk diamond province of Russia to provide new insights into multi-stage metasomatism in the subcratonic lithospheric mantle(SCLM)and the origin of phlogopite in kimberlite.Based on the analysed xenoliths,phlogopite is characterized by several generations.The first generation(Phil)occurs as coarse,discrete grains within garnet peridotite and eclogite xenoliths and as a rock-forming mineral within clinopyroxene-phlogopite xenoliths.The second phlogopite generation(Phl2)occurs as rims and outer zones that surround the Phil grains and as fine flakes within kimberlite-related veinlets filled with carbonate,serpentine,chlorite and spinel.In garnet peridotite xenoliths,phlogopite occurs as overgrowths surrounding garnet porphyroblasts,within which phlogopite is associated with Cr-spinel and minor carbonate.In eclogite xenoliths,phlogopite occasionally associates with carbonate bearing veinlet networks.Phlogopite,from the kimberlite,occurs as megacrysts,macrocrysts,microcrysts and fine flakes in the groundmass and matrix of kimberlitic pyroclasts.Most phlogopite grains within the kimberlite are characterised by signs of deformation and form partly fragmented grains,which indicates that they are the disintegrated fragments of previously larger grains.Phil,within the garnet peridotite and clinopyroxene-phlogopite xenoliths,is characterised by low Ti and Cr contents(TiO_21 wt.%,Cr_2 O_31 wt.% and Mg# = 100 × Mg/(Mg+ Fe)92)typical of primary peridotite phlogopite in mantle peridotite xenoliths from global kimberlite occurrences.They formed during SCLM metasomatism that led to a transformation from garnet peridotite to clinopyroxene-phlogopite rocks and the crystallisation of phlogopite and high-Cr clinopyroxene megacrysts before the generation of host-kimberlite magmas.One of the possible processes to generate low-Ti-Cr phlogopite is via the replacement of garnet during its interaction with a metasomatic agent enriched in K and H_2O.Rb-Sr isotopic data indicates that the metasomatic agent had a contribution of more radiogenic source than the host-kimberlite magma.Compared with peridotite xenoliths,eclogite xenoliths feature low-Ti phlogopites that are depleted in Cr_2O_3 despite a wider range of TiO_2 concentrations.The presence of phlogopite in eclogite xenoliths indicates that metasomatic processes affected peridotite as well as eclogite within the SCLM beneath the Grib kimberlite.Phl2 has high Ti and Cr concentrations(TiO_22 wt.%,Cr_2O_31 wt.% and Mg# = 100× Mg/(Mg + Fe)92)and compositionally overlaps with phlogopite from polymict brecc:ia xenoliths that occur in global kimberlite formations.These phlogopites are the product of kimberlitic magma and mantle rock interaction at mantle depths where Phl2 overgrew Phil grains or crystallized directly from stalled batches of kimberlitic magmas.Megacrysts,most macrocrysts and microcrysts are disintegrated phlogopite fragments from metasomatised peridotite and eclogite xenoliths.Fine phlogopite flakes within kimberlite groundmass represent mixing of high-Ti-Cr phlogopite antecrysts and high-Ti and low-Cr kimberlitic phlogopite with high Al and Ba contents that may have formed individual grains or overgrown antecrysts.Based on the results of this study,we propose a schematic model of SCLM metasomatism involving phlogopite crystallization,megacryst formation,and genesis of kimberlite magmas as recorded by the Grib pipe.  相似文献   

9.
Garnets from phlogopite harzburgite xenoliths from the Wesselton kimberlite show zoning from low-Ca harzburgitic cores to rims with lherzolitic Ca-Cr relations. Garnet cores are depleted in Y and HREE, but have sinuous REE patterns enriched in the MREE. Rimwards increase in Ca and decrease in Cr and Mg is accompanied by increases in Zr, Y, Ti and HREE. Secondary replacement rims on some garnets consist of garnet with low Ca and Cr, but high Mg, Ti and HREE. The zoning, and the secondary replacement rims, are attributed to different stages of a metasomatic process that has converted harzburgite to lherzolite, at temperatures near 1000 °C. Modelling of zoning profiles suggests that the process can be divided into three parts: (a) Inwards diffusion of Ca, Zr and Y over periods of 10,000–30,000 years, from a fluid depleted in Ti, Ga and Y; (b) formation of overgrowths high in Ca, Zr, Y and Ti, followed by annealing over periods of several thousand years; (c) formation of secondary reaction rims of low-Ca garnet, on very short timescales prior to eruption. The sinuous REE patterns of the garnet cores are regarded as “primary” features reflecting an ancient metasomatic event superimposed on a depleted protolith. The high Zr/Y, Zr/Ti and Zr/Ca of the fluids corresponding to stage (a) are ascribed to the presence of phlogopite and garnet in the matrix near the fluid source (presumed to be a melt, possibly a kimberlite precursor), leading to the development of concentration fronts in the percolating fluid. The overgrowths of stage (b) appear to coincide with the precipitation of phlogopite in the rock. The low Ca of the fluid responsible for the secondary replacement rims of stage (c) may reflect the late precipitation of clinopyroxene or Ca-carbonate as part of the metasomatic assemblage. These processes have significantly modified the modal, major- and trace-element composition of the mantle volume sampled by the Wesselton kimberlite, within <1 Ma of eruption. Recognition of such effects and their distribution in time and space is essential to understanding of the evolution of the subcontinental lithospheric mantle. Received: 11 February 1998 / Accepted: 24 June 1998  相似文献   

10.
Summary Garnet occurs as a significant mineral constituent of felsic garnet-biotite granite in the southern edge of the Třebíč pluton. Two textural groups of garnet were recognized on the basis of their shape and relationship to biotite. Group I garnets are 1.5–2.5 mm, euhedral grains which have no reaction relationship with biotite. They are zoned having high XMn at the rims and are considered as magmatic. Group II garnets form grain aggregates up to 2.5 cm in size, with anhedral shape of individual grains. The individual garnet II grains are usually rimmed by biotite and have no compositional zoning. The core of group I garnets and group II garnets contains 67–80 mol% of almandine, 5–19 mol% of pyrope, 7–17 mol% of spessartine and 2–4 mol% of grossular. Biotite occurs in two generations; both are magnesian siderophyllites with Fe/(Fe + Mg) = 0.50–0.69. The matrix biotite in granites (biotite I) has high Ti content (0.09–0.31 apfu) and Fe/(Fe + Mg) ratio between 0.50 and 0.59. Biotite II forms reaction rims around garnet, is poor in Ti (0.00–0.06 apfu) and has a Fe/(Fe + Mg) ratio between 0.61 and 0.69. The textural relationship between biotite and garnet indicates that garnet reacted with granitic melt to form Ti-poor biotite and a new granitic melt, depleted in Ti and Mg and enriched in Fe and Al. In contrast to the host durbachites (hornblende-biotite melagranites), which originated by mixing of crustal melts and upper mantle melts, the origin of garnet-bearing granites is related to partial melting of the aluminium-rich metamorphic series of the Moldanubian Zone.  相似文献   

11.
Garnet of eclogite (formerly termed garnet clinopyroxenite) hosted in lenses of orogenic garnet peridotite from the Granulitgebirge, NW Bohemian Massif, contains unique inclusions of granitic melt, now either glassy or crystallized. Analysed glasses and re-homogenized inclusions are hydrous, peraluminous, and enriched in highly incompatible elements characteristic of the continental crust such as Cs, Li, B, Pb, Rb, Th, and U. The original melt thus represents a pristine, chemically evolved metasomatic agent, which infiltrated the mantle via deep continental subduction during the Variscan orogeny. The bulk chemical composition of the studied eclogites is similar to that of Fe-rich basalt and the enrichment in LILE and U suggest a subduction-related component. All these geochemical features confirm metasomatism. In comparison with many other garnet+clinopyroxene-bearing lenses in peridotites of the Bohemian Massif, the studied samples from Rubinberg and Klatschmühle are more akin to eclogite than pyroxenites, as reflected in high jadeite content in clinopyroxene, relatively low Mg, Cr, and Ni but relatively high Ti. However, trace elements of both bulk rock and individual mineral phases show also important differences making these samples rather unique. Metasomatism involving a melt requiring a trace element pattern very similar to the composition reported here has been suggested for the source region of rocks of the so-called durbachite suite, that is, ultrapotassic melanosyenites, which are found throughout the high-grade Variscan basement. Moreover, the Th, U, Pb, Nb, Ta, and Ti patterns of these newly studied melt inclusions (MI) strongly resemble those observed for peridotite and its enclosed pyroxenite from the T-7 borehole (Staré, České Středhoři Mountains) in N Bohemia. This suggests that a similar kind of crustal-derived melt also occurred here. This study of granitic MI in eclogites from peridotites has provided the first direct characterization of a preserved metasomatic melt, possibly responsible for the metasomatism of several parts of the mantle in the Variscides.  相似文献   

12.
Cathodoluminescence (CL) of quartz from metamorphic rocks representing a range of conditions from the garnet grade to the migmatite grade reveals a variety of textures, that is, a function of metamorphic grade and deformation history. Ti concentrations, determined by electron microprobe and ion microprobe, generally correlate with CL intensity (blue wavelengths), and application of the Ti‐in‐quartz thermometer (TitaniQ) reflects the temperature of quartz growth or recrystallization, and, in some settings, modification by diffusion. Quartz from garnet grade samples is not visibly zoned, records temperatures of 425–475 °C, and is interpreted to have recrystallized during fabric formation. Quartz grains from staurolite grade samples are zoned in CL with markedly darker cores and brighter rims, some of which are interpreted to have been produced by the dominant staurolite‐producing reaction, whereas others are interpreted as having formed by diffusion of Ti into quartz rims. Quartz from the matrix of kyanite and sillimanite grade samples are generally unzoned, although locally displays slightly brighter rims (higher Ti); quartz inclusions within garnet and staurolite have distinctly brighter rims, which are interpreted as having been produced by diffusive exchange with the host mineral. Quartz from migmatite grade samples displays highly variable CL intensity, which is dependent on the location of the grain. Matrix grains in melanosomes are largely unzoned or rarely zoned with darker cores. Leucosome quartz is strongly zoned with bright cores and dark rims and is interpreted as having formed during crystallization of the melt. Locally within the leucosome is observed oscillatory‐zoned quartz, which is interpreted as a subsolidus recrystallization to achieve strain relaxation. Quartz inclusions within garnet or plagioclase crystals often show bright domains separated by zones of dark CL. These enigmatic textures possibly reflect local melting fluxed by fluid inclusions. Temperatures calculated from the Ti–in–quartz thermometer are a function of the metamorphic grade of the sample, the textural setting of the quartz, the reaction history and the deformation history of the rock. The TitaniQ temperatures can be used to constrain the conditions at which various metamorphic processes have occurred.  相似文献   

13.
Compositional zonation in garnets in peridotite xenoliths   总被引：1，自引：0，他引：1  
Garnets in 42 peridotite xenoliths, most from southern Africa, have been analyzed by electron probe to seek correlations between compositional zonation and rock history. Xenoliths have been placed into the following 6 groups, based primarily upon zonation in garnet: I (12 rocks)-zonation dominated by enrichment of Ti and other incompatible elements in garnet rims; II (10 rocks)-garnet nearly homogeneous; III (8 rocks)-rims depleted in Cr, with little or no related zonation of Ti; IV (3 rocks)-slight Ti zonation sympathetic to that of Cr; V (3 rocks)-garnet rims depleted or enriched in Cr, and chromite included in garnet; VI (6 rocks)-garnets with other characteristics. Element partitioning between olivine, pyroxene, and garnet rims generally is consistent with the assumption of equilibrium before eruption. Although one analyzed rock contains olivine and pyroxene that may have non-equilibrated oxygen isotopes, no corresponding departures from chemical equilibrium were noted. Causes of zoning include melt infiltration and changes in temperature and pressure. Zonation was caused or heavily influenced by melt infiltration in garnets of Group I. In Groups III, IV, and V, most compositional gradients in garnets are attributed to changes in temperature, pressure, or both, and gradients of Cr are characteristic. There are no simple relationships among wt% Cr2O3 in garnet, calculated temperature, and the presence of compositional gradients. Rather, garnets nearly homogeneous in Cr are present in rocks with calculated equilibration temperatures that span the range 800–1500 °C. Although the most prominent Cr gradients are found in relatively Cr-rich garnets of rocks for which calculated temperatures are below 1050 °C, gradients are well-defined in a Group IV rock with T1300 °C. The variety of Cr gradients in garnets erupted from a range of temperatures indicates that the zonations record diverse histories. Petrologic histories have been investigated by simulated cooling of model rock compositions in the system CaO–MgO–Al2O3–SiO2–Cr2O3. Proportions and compositions of pyroxene and garnet were calculated as functions of P and T. The most common pattern of zonation in Groups III and IV, a decrease of less than 1 wt% Cr2O3 core-to-rim, can be simulated by cooling of less than 200 °C or pressure decreases of less than 1 GPa. The preservation of growth zonation in garnets with calculated temperatures near 1300 °C implies that these garnets grew within a geologically short time before eruption, probably in response to fast cooling after crystallization of a small intrusion nearby. Progress in interpreting garnet zonations in part will depend upon determinations of diffusion rates for Cr. Zonation formed by diffusion within garnet cannot always be distinguished from that formed by growth, but Ca–Cr correlations unlike those typical of peridotite suite garnets may document diffusion.  相似文献   

14.
The Quaternary foidites and basanites of the West Eifel (Germany) contain optically and chemically heterogeneous clinopyroxenes, some of which occur as discrete zones within individual crystals: Most clinopyroxene phenocrysts are made up of a core and a normally zoned comagmatic titanaugite mantle. Most cores are greenish pleochroic and moderately resorbed (fassaitic augite). Some are pale green and strongly resorbed (acmitic augite). Cores of Al-augite composition and of Cr-diopside derived from peridotite xenoliths are rare. The fassaitic augites are similar in trace element distribution pattern to the titanaugites, but are more enriched in incompatible elements. The acmitic augites, in contrast, are clearly different in their trace element composition and are enriched in Na, Mn, Fe and depleted in Al, Ti, Sr, Zr. A model for polybaric magma evolution in the West Eifel is proposed: Primitive alkali basaltic magma rises through the upper mantle precipitating Al-augite en route. It stagnates and differentiates near the crust/mantle boundary crystallizing Fe-rich fassaitic augites. The magma differentiated at high pressure is subsequently mixed with new pulses of primitive magma from which the rims of pyroxene are crystallized. Sporadic alkali pyroxenite xenoliths are interpreted to represent cumulates of cognate phases formed within the crust and not metasomatized upper mantle material (Lloyd and Bailey 1975).  相似文献   

15.
We report the field, petrographic and mineral chemical characteristics of relict super‐silicic (=majoritic) garnet microstructures from the Otrøy peridotites in the Western Gneiss Region, Norway. The evidence for the former existence of super‐silicic garnet consists of two‐pyroxene exsolution microstructures from garnet. Estimates of the initial composition of the super‐silicic garnet imply pressures of 6–6.5 GPa, indicating that the Otrøy garnet peridotites were derived from depths >185 km. The garnet peridotites consist of inter‐banded variable compositions with c. 50% garnet peridotite and 50% garnet‐free peridotite. Two distinct garnet types were identified: (a) normal matrix garnet, grain‐size ≤4 mm, and (b) large isolated single garnet crystals and/or (polycrystalline) garnet nodules up to 10 cm in size. Large garnet nodules occur only within limited bands within the garnet peridotites. The relicts of super‐silicic garnet were exclusively found in some (not all) of the larger garnet nodules. Petrographic observations revealed that the microstructure of nodular garnet consists of the following four characteristic elements. (1) Individual garnet nodules are polycrystalline, with grain sizes of 2–8 mm. Garnet grain boundaries are straight with well‐defined triple junctions. (2) Some garnet triple junctions and garnet grain boundaries are decorated by interstitial orthopyroxene. (3) Cores of larger polycrystalline garnet contain two‐pyroxene exsolution microstructures. (4) Precipitation‐free rims (2 mm thick) surround garnet cores containing the exsolved pyroxene microstructure. Pyroxene exsolution from super‐silicic garnet was subsequently followed by brittle–ductile deformation of garnet. Both exsolved pyroxene needles and laths become undulous or truncated by fractures. Simultaneous garnet plasticity is indicated by the occurrence of high densities of naturally decorated dislocations. Transmission electron microscopy observations indicate that decoration is due to Ti‐oxide precipitation. Estimates of the P–T conditions for mineral chemical equilibration were obtained from geothermobarometry. The mineral compositions equilibrated at mantle conditions around 805±40 °C and 3.2±0.2 GPa. These P–T estimates correspond to cold continental lithosphere conditions at depths of around 105 km. From a combination of both depth estimates it can be concluded that the microstructural memory of the rock extends backwards to twice as great a depth range as obtained by thermobarometric methods. Available geochronological and geochemical data of Norwegian garnet peridotites suggest a multi‐stage, multi‐orogenic exhumation history.  相似文献   

16.
Crystal fragments of pyrope from diatremes of ultramafic microbreccia in the Navajo Province of the Colorado Plateau contain inclusions of olivine, pyroxene, spinel, chlorite, amphibole, chlorapatite, and dolomite. The included suite supports earlier hypotheses that hydrous phases and carbonates were primary parts of some garnet peridotite assemblages in the Plateau lithosphere. Garnets with spinel and orthopyroxene inclusions likely all were sampled at pressures less than 36 kb and perhaps as low as 15–20 kb; no evidence was found for inclusions from greater depths. Temperature estimates are 800°–900° C for garnet-clinopyroxene equilibration, but only 500°–700° C for garnetolivine equilibration. Inherent differences between geothermometry methods account for only part of the discrepancy. Pronounced Fe-Mg zoning in garnet at olivine contacts and the lack of such zoning at clinopyroxene contacts are evidence that the difference in part relates to relative reequilibration rates with cooling. The garnet-olivine temperature estimates may be the best approximations to mantle temperatures before eruption. Our data are compatible both with the hypothesis that the garnet peridotite was emplaced in the mantle by large-scale, horizontal transport in the lithosphere and with the hypothesis that rocks were sampled from Precambrian lithosphere cooled to temperatures like those along a low heat flow geotherm. Discordances between the geothermometers here and in other lherzolite localities may be keys to evaluating tectonic histories of lherzolite masses.  相似文献   

17.
《International Geology Review》2012,54(12):1506-1522
Garnet orthopyroxenites from Maowu (Dabieshan orogen, eastern China) were formed from a refractory harzburgite/dunite protolith. They preserve mineralogical and geochemical evidence of hydration/metasomatism and dehydration at the lower edge of a cold mantle wedge. Abundant polyphase inclusions in the cores of garnet porphyroblasts record the earliest metamorphism and metasomatism in garnet orthopyroxenites. They are mainly composed of pargasitic amphibole, gedrite, chlorite, talc, phlogopite, and Cl-apatite, with minor anhydrous minerals such as orthopyroxene, sapphirine, spinel, and rutile. Most of these phases have high XMg, NiO, and Ni/Mg values, implying that they probably inherited the chemistry of pre-existing olivine. Trace element analyses indicate that polyphase inclusions are enriched in large ion lithophile elements (LILE), light rare earth elements (LREE), and high field strength elements (HFSE), with spikes of Ba, Pb, U, and high U/Th. Based on the P–T conditions of formation for the polyphase inclusions (?1.4 GPa, 720–850°C), we suggest that the protolith likely underwent significant hydration/metasomatism by slab-derived fluid under shallow–wet–cold mantle wedge corner conditions beneath the forearc. When the hydrated rocks were subducted into a deep–cold mantle wedge zone and underwent high-pressure–ultrahigh-pressure (HP–UHP) metamorphism, amphibole, talc, and chlorite dehydrated and garnet, orthopyroxene, Ti-chondrodite, and Ti-clinohumite formed during prograde metamorphism. The majority of LILE (e.g. Ba, U, Pb, Sr, and Th) and LREE were released into the fluid formed by dehydration reactions, whereas HFSE (e.g. Ti, Nb, and Ta) remained in the cold mantle wedge lower margin. Such fluid resembling the trace element characteristics of arc magmas evidently migrates into the overlying, internal, hotter part of the mantle wedge, thus resulting in a high degree of partial melting and the formation of arc magmas.  相似文献   

18.
碳酸盐熔体交代作用是指在地幔碳酸盐熔体与橄榄岩之间的相互作用,是改造地幔的重要方式之一.碳酸盐熔体交代会显著改变地幔橄榄岩的岩石学和地球化学特征.首先,碳酸盐熔体交代作用会改变地幔橄榄岩中的矿物组成和比例.尽管碳酸盐熔体与橄榄岩的反应结果受控于初始反应物成分和反应的温压条件,但多数反应会导致橄榄岩中辉石的比例增加,而且有时还会出现磷灰石、独居石等副矿物.另外,在有些受碳酸盐熔体交代显著的橄榄岩的矿物中不仅可发现大量CO2流体包裹体和碳酸盐熔体包裹体,也会出现特殊的反应边结构和熔体囊.其次,碳酸盐熔体在改造地幔橄榄岩过程中,会在地幔矿物中留下明显的地球化学指纹.在主量元素特征上,受到碳酸盐熔体交代的橄榄岩中的单斜辉石往往具有偏高的Mg#和Ca/Al比值（>5）;而在微量元素组成特征上的变化更为显著,包括单斜辉石具有高的（La/Yb）N、Eu/Ti、Zr/Hf、Y/Ho比值,并显著亏损HFSE等.另外,值得注意的是,碳酸盐熔体与地幔橄榄岩反应的程度不同也会导致这些地球化学特征存在差异,因此在判别碳酸盐熔体交代作用时要采用岩石学和地球化学特征相结合,多方面对比分析.对于引起地幔碳酸盐熔体交代作用的交代介质来源的识别主要用Mg-Zn-Ca-Sr等多种同位素体系进行示踪研究,尤其是近年来微区Sr同位素分析方法的建立为地幔碳酸盐熔体交代作用研究提供了重要手段.   相似文献   

19.
Proton microprobe (PIXE) analysis of garnet, pyroxene, and olivine for Zr, Y, Ga, Ge, Sr, Ni, Mn and Zn has been combined with electron-probe and petrographic analysis to interpret the histories of garnetperidotite xenoliths from the minette neck at The Thumb on the Colorado Plateau. Garnet in seven rocks contains 10–110 ppm Zr and 25–95 ppm Ni. Substantial parts of these ranges are preserved in single, zoned garnets (Zr, 25–90 ppm; Ni, 25–60 ppm). Pyroxene and olivine are more homogeneous and equilibrated more quickly than granet to changing temperatures and metasomatic fluxes. The distribution coefficient of Ti between pyroxene and garnet rims may be sufficiently sensitive to pressure to be used as a geobarometer. Zirconium and Ti appear to have behaved similarly during melt infiltration and diffusion within garnet. Nickel in garnet is a sensitive recorder of temperature. A temperature of 900° C or less calculated from Ni in the cores of large garnets in one rock is at least as cool as that calculated for the Archaean Kaapvaal craton at similar depth, and the low temperature may be due to cooling of the Plateau lithosphere by the subducted Farallon plate. The zonation of these garnets to Ni-enriched rims has been simulated numerically by heating 260° C at 0.02°/year, followed by overgrowth of a rim and short annealing. Garnet in another rock records a temperature decrease of about 70° C, but Ni is more homogeneous in garnets in the other five rocks. The diverse temperature histories are attributed to local melt-mantle interactions. Calculated pressures and temperatures of xenoliths from The Thumb form a grouping similar to those for high-temperature parts of inflected geotherms in other xenolith suites, and the similarity is evidence for both the reality and the transients nature of the calculated inflections. Garnet that is zoned in Zr, Y, Ti and other elements preserves evidences for grain growth in response to melt infiltration in four of seven rocks. The ranges of both major and trace elements in the xenolith suite may be due largely to enrichment processes following earlier depletion.  相似文献   

20.
Electron microprobe analyses sensitive to 20ppmw (2σ) were made for Na, P, K and Ti in garnet, pyroxenes and olivine from peridotite and eclogite xenoliths from African kimberlites and volcanic rocks in Tanzania. Average concentrations (ppmw) in peridotite (mostly garnet lherzolite) are: Na2O gt 340 ol 90 opx 1070 cpx 2.1 (wt.%); P2O5 gt 460 ol 130 opx 50 cpx 350; K2O gt <20 ol <20 opx 30 cpx 170; TiO2 gt 1470 ol 130 opx 480 cpx 1630. For eclogites and a cpx megacryst with gt inclusions: Na2O gt 610 cpx 4.3 (wt.%); P2O5 gt 530 cpx 300; K2O gt <20 cpx 370; TiO2 gt 1990 cpx 1980.In garnet, Na can be explained by coupled substitution with P and Ti, and there is no need to invoke six-coordinated silicon. The Na distribution between garnet and clinopyroxene correlates with the Fe/Mg distribution for both eclogites and peridotites, and for the peridotites correlates with estimates of pressure and temperature from pyroxene composition. When calibrated experimentally, the Na distribution may be a useful indicator of physical conditions at depths for which the Fe/Mg distribution is insensitive; furthermore the Na distribution may be less sensitive to oxidation state.  相似文献   

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