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1.
An alkali basalt near Glen Innes, northeastern New South Wales, contains a suite of Cr-diopside group ultramafic xenoliths which includes some spinel peridotites but which is dominated by a diverse spinel pyroxenite assemblage. Pyroxenite xenoliths range from subcalcic clinopyroxenites (composed largely of unmixed prismatic subcalcic clinopyroxene megacrystals and lesser orthopyroxene megacrystals) to equant mosaic textured websterites (orthopyroxene and Ca-rich clinopyroxene ± spinel). Rare orthopyroxenite xenoliths also occur. The pyroxenite xenoliths are characterised by high 100Mg/(Mg + Fe2+) ratios (M˜ 90) and low concentrations of Ti, K, P, La, Ce and Zr. The websterites are mineralogically and chemically similar to many spinel pyroxenites occurring as layers or dykes in peridotite massifs such as those at Ronda in southern Spain and at Ariège (French Pyrénées). T / P estimates indicate crystallization temperatures of 1250–1350 °C for subcalcic clinopyroxene-orthopyroxene megacrystal pairs and 900–1000 °C for the equilibrated mosaic textured websterites and associated peridotites at pressures of 9–13 kbar. Subcalcic clinopyroxene megacrystals, websterites and orthopyroxenites have LREE-depleted chondrite-normalised REE abundances with (La/Yb)CN < 1 and their convex-upwards REE patterns are typical of subcalcic clinopyroxene-dominated cumulates. The pyroxenites are not residua from partially melted pyroxenite layers or dykes in mantle peridotites nor are they completely crystallized protobasaltic or protopicritic magmas. They are interpreted as high-pressure crystal segregations from basaltic magmas (probably mildly alkaline or transitional) flowing within narrow mantle conduits (the flow crystallization model of Irving, 1980). The parental magma(s) was Ti-poor (0.6–0.7% TiO2) and relatively Mg-rich (M˜ 74 − 70). Pyroxenite genesis was a two-stage process involving crystallization of tschermakitic subcalcic clinopyroxenes and orthopyroxenes  ±spinel as liquidus or near-liquidus phases at 1250–1350 °C and 9–13 kbar to yield “primary” subcalcic clinopyroxenites which then re-equilibrated at 900–1000 °C and similar pressures to produce the mosaic textured “secondary” websterites. The pyroxenites show a wide range of 143Nd/144Nd and 87Sr/86Sr values (0.513298–0.512473 and 0.702689–0.704659, respectively). Their isotopic ratios appear to have been variably modified by exchange with adjacent mantle peridotites or migrating basaltic melts. Received: 11 December 1995 / Accepted: 3 December 1996  相似文献   

2.
 A pronounced negative correlation between the yttrium concentration in garnet ([Y]Grt) and temperature has been observed in xenotime (YPO4)-bearing metapelites from central New England, USA. The [Y]Grt decreases roughly two orders of magnitude (∼5500 to less than 100 ppm Y) over a 150 °C interval. A regression of ln([Y]Grt) against estimated reciprocal temperature yields the following relationship:
with R2 = 0.97. The decrease in garnet Y content is most rapid over garnet- to staurolite-zone conditions (450–550 °C) and the thermometer has a precision of a few degrees in this range. Received: 21 January 1999 / Accepted: 13 September 1999  相似文献   

3.
The near-solidus transition from garnet lherzolite to spinel lherzolite   总被引：20，自引：1，他引：19  
The position of the transition from spinel lherzolite to garnet lherzolite in the system CaO-MgO-Al2O3-SiO2 (CMAS) has been determined experimentally at near-solidus temperatures. In reversed experiments, the transition occurs between 18 and 20 kbar at 1200 °C and between 26 and 27 kbar at 1500 °C, corresponding to higher pressures than previously envisaged. A position for the transition deeper within the Earth further complicates the explanation of the so-called garnet signatures in the trace element and isotope patterns of mid-ocean ridge basalts. If melting during adiabatic upwelling beneath a mid-ocean ridge begins at the depth required for the stability of garnet in peridotitic compositions, simple melting models predict that the amount of melt produced should be much greater than the observed thickness of the oceanic crust. A partial solution to the apparent conflict might be that (1) the rather simplistic melting models are in error, (2) that melting begins in garnet pyroxenite veins that are believed to be stable at lower pressures than garnet lherzolite or (3) that melting does not involve garnet at all, but it is clinopyroxene causing the trace element patterns observed in basalts erupted at mid-ocean ridges. A second set of reversal experiments were conducted to investigate the solubility of alumina in both orthopyroxenes and clinopyroxenes at the high temperatures near the solidus in the system CMAS. The results are compatible with most previous studies, and may be used as a starting point to calibrate thermodynamic models for pyroxenes in chemical systems, approximating upper mantle chemistry. Received: 9 August 1999 / Accepted: 29 October 1999  相似文献   

4.
Diamonds and their syngenetic mineral inclusions from placer deposits (Akwatia mine) along the Birim River, Ghana were studied, thus providing the first detailed data collection for the West African Craton. Inclusion contents indicate an almost exclusively peridotitic diamond suite, with the vast majority being part of the harzburgitic paragenesis. Chemically the Akwatian diamond inclusions differ from those in our 1100 sample world-wide data base mainly by shifts towards lower Mg/Fe ratios for harzburgitic olivines and orthopyroxenes, extremely high Ni contents in both harzburgitic and lherzolitic olivines, and a higher mean Cr content in chromites. The inconsistency between the low Mg/Fe ratios and the highly refractory compatible trace element signature seems best to be explained by re-fertilisation of a previously depleted source, similar to the metasomatic re-enrichment of deformed, Fe-Ti-rich and hot peridotites discussed by Harte (1983). Geothermometry shows Akwatian inclusions to be 140–190 °C hotter than the peridotitic average (1050 °C) given by Harris (1992). Since garnet-opx equilibria (1100 °C/50 kbar to 1370 °C/67 kbar) indicate a typical shield geotherm (40–42 mW/m2), these elevated temperatures imply an origin of the Akwatian diamonds unusually deep for a peridotitic suite. This is consistent with the presence of extraordinary amounts of silicate spinel component in chromite inclusions, indicative of crystallisation under higher pressures than recorded for most peridotitic suites. In addition, one garnet showed the highest knorringite component (66.4 mol%) so far observed in an inclusion in diamond. The same garnet also contained a minor enstatite solid-solution component, which indicates crystallisation at pressures just below 80 kbar. Akwatian diamond inclusions, therefore, represent the most complete cross-section through peridotitic subcontinental lithospheric upper mantle so far observed, down to a maximum depth between 200–240 km. Received: 1 November 1995 / Accepted 5 January 1997  相似文献   

5.
An eclogite barometer has profound importance in the study of upper mantle processes and potential application to diamond prospecting. Studies on the partitioning of Li between clinopyroxene (cpx) and garnet (grt) in natural samples have shown that this particular element is very sensitive to changes in pressure and could be calibrated as the barometer demanded for bimineralic eclogites. Experiments were performed from 4 to 13 GPa and 1,100–1,400°C in the CMAS (CaO, MgO, Al2O3, SiO2) system with Li added as Li3PO4 to quantify this pressure dependence into a barometer expressed in the following equation: P = (0.00255T – ln K d)/0.2351 where P is in GPa, T is in °C and K d is defined as the partition coefficient of Li (in ppm) between clinopyroxene and garnet. The experimental pressures are reproduced to ±0.38 GPa (1σ) by this equation. This barometer is strictly applicable only to CMAS. Experiments at 1,300°C, 8–12 GPa showed that Henry’s Law is fulfilled for Li partitioning between cpx and grt in the concentration range of approximately 0.01–1 wt% Li. Direct application of the equation to experiments in natural systems performed at 1,300°C from 4 to 13 GPa consistently overestimates pressures by approximately 2 GPa. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

6.
An experimental study of Ca-(Fe,Mg) interdiffusion in silicate garnets   总被引：1，自引：0，他引：1  
Ca-(Fe,Mg) interdiffusion experiments between natural single crystals of grossular (Ca2.74Mg0.15 Fe0.23Al1.76Cr0.04Si3.05O12) and almandine (Ca0.21Mg0.40 Fe2.23Mn0.13Al2.00Cr0.08Si2.99O12 or Ca0.43Mg0.36Fe2.11 Al1.95Si3.04O12), were undertaken at 900–1100 °C and 30 kbar, and pressures of 15.0–32.5 kbar at 1000 °C. Samples were buffered by Fe/FeO in most cases. Diffusion profiles were determined by electron microprobe. Across the experimental couples the interdiffusion coefficients (D˜) were almost independent of composition. The diffusion rates in an unbuffered sample were significantly faster than in buffered samples. The temperature dependence of the D˜ (Ca-Fe,Mg) interdiffusion coefficients may be described by
at 30 kbar and 900–1100 °C. This activation energy is marginally higher than previous experimental studies involving Ca-free garnets; the interdiffusion coefficients are higher than previous studies for Fe-Mg and Fe-Mn exchange in garnet. The pressure dependence of D˜ (Ca-Fe,Mg) at 1000 °C yielded an activation volume of 11.2 cm3 mol−1, which is higher than previous results from studies involving garnet and olivine. Comparison with simulation studies suggests a vacancy mechanism for divalent ion migration in garnet, with extrinsic processes being dominant up to very high temperatures. Received: 15 December 1996 / Accepted: 3 November 1998  相似文献   

7.
Quantitative thermobarometry of inclusions in zoned garnet from a Franciscan eclogite block record a counter-clockwise P–T path from blueschist to eclogite and back. Garnet retains prograde zoning from inclusion-rich Alm52Grs30Pyp6Sps12 cores to inclusion-poor Alm62Grs25Pyp12Sps1 mantles, with overgrowths of highly variable composition. Barometry using the Waters–Martin version of the garnet–phengite–omphacite thermobarometer yields conditions of 7–15 kbar, 400–500°C (garnet cores), 18–22 kbar, ∼550°C (mantles), and 10–14 kbar, 350–450°C (overgrowths), in agreement with clinozoisite–sphene–rutile–garnet–quartz barometry. These pressures are ∼10–15 kbar less than those obtained using more recent, fully thermodynamic calibrations of the phengite–omphacite–garnet thermobarometer. Low early temperatures suggest that the block was subducted in a thermally mature subduction zone and not at the inception of subduction when prograde temperature is expected to be higher. Franciscan high-grade blocks likely represent crust subducted throughout the history of this convergent margin, rather than only at the inception of the subduction zone.  相似文献   

8.
The garnet–biotite–muscovite–plagioclase (GBMP) barometer was empirically revised for P–T conditions of 1–14 kbar and 450–840 °C, using 263 metapelitic rock samples from all over the world. This barometer is based on activity models for garnet, biotite and plagioclase identical to those of the well‐calibrated garnet–biotite thermometer and the garnet–aluminosilicate–plagioclase–quartz (GASP) barometer. The GBMP barometer is less temperature dependent than the GASP barometer and can be applied to either Al2SiO5‐absent or Al2SiO5‐bearing metapelites. The total error of the GBMP barometer is estimated to be about ±1.2 kbar on considering input temperature error and analytical errors of chemical compositions of the phases involved. The random error of the GBMP barometer is evenly distributed with respect to pressure, temperature and mineral composition. Simultaneous application of the GBMP barometer and the garnet–biotite thermometer identifies the correct stability field for Al2SiO5‐bearing metapelites. Application of the GBMP barometer to metapelitic rocks within the same geological terranes or thermal contact aureoles yielded similar pressures within error. A spreadsheet for implementing the proposed GBMP geobarometer is supplied on the journal's website.  相似文献   

9.
The Lherz orogenic lherzolite massif (Eastern French Pyrenees) displays one of the best exposures of subcontinental lithospheric mantle containing veins of amphibole pyroxenites and hornblendites. A reappraisal of the petrogenesis of these rocks has been attempted from a comprehensive study of their mutual structural relationships, their petrography and their mineral compositions. Amphibole pyroxenites comprise clinopyroxene, orthopyroxene and spinel as early cumulus phases, with garnet and late-magmatic K2O-poor pargasite replacing clinopyroxene, and subsolidus exsolution products (olivine, spinel II, garnet II, plagioclase). The original magmatic mineralogy and rock compositions were partly obscured by late-intrusive hornblendites and over a few centimetres by vein–wallrock exchange reactions which continued down to subsolidus temperatures for Mg–Fe. Thermobarometric data and liquidus parageneses indicate that amphibole pyroxenites started to crystallize at P ≥ 13 kbar and recrystallized at P < 12 kbar. The high AlVI/AlIV ratio (>1) of clinopyroxenes, the early precipitation of orthopyroxene and the late-magmatic amphibole are arguments for parental melts richer in silica but poorer in water than alkali basalts. Their modelled major element compositions are similar to transitional alkali basalt with about 1–3 wt% H2O. In contrast to amphibole pyroxenites, hornblendites only show kaersutite as liquidus phase, and phlogopite as intercumulus phase. They are interpreted as crystalline segregates from primary basanitic magmas (mg=0.6; 4–6 wt% H2O). These latter cannot be related to the parental liquids of amphibole pyroxenites by a fractional crystallization process. Rather, basanitic liquids mostly reused pre-existing pyroxenite vein conduits at a higher structural level (P ≤ 10 kbar). A continuous process of redox melting and/or alkali melt/peridotite interaction in a veined lithospheric mantle is proposed to account for the origin of the Lherz hydrous veins. The transitional basalt composition is interpreted in terms of extensive dissolution of olivine and orthopyroxene from wallrock peridotite by alkaline melts produced at the mechanical boundary layer/thermal boundary layer transition (about 45–50 km deep). Continuous fluid ingress allowed remelting of the deeper veined mantle to produce the basanitic, strongly volatiles enriched, melts that precipitated hornblendites. A similar model could be valid for the few orthopyroxene-rich hydrous pyroxenites described in basalt-hosted mantle xenoliths. Received: 15 September 1999 / Accepted: 31 January 2000  相似文献   

10.
The crystal structures of 212 experimentally synthesized, igneous clinopyroxenes were modeled from electronprobe chemical data. The coexisting melts span a wide range of petrologically relevant, dry and hydrous compositions, characterized by variable enrichment in silica and alkalis. Experimental conditions pertain to Earth's crust and uppermost mantle (P = 0–24 kbar; garnet absent) and a variety of f O2 values (from CCO-buffered to air-buffered) and mineral assemblages (Cpx ± Opx ± Pig ± Ol ± Plag ± Spl ± Mt ± Amp ± Ilm). Unit-cell volume (Vcell) versus M1-polyhedron volume (VM1) relations were investigated over a range of pressures and temperatures using data derived from structure modeling and corrected for thermal expansivity and compressibility. The relationships between pressure and clinopyroxene structural parameters were found to be dependent on the nature of the coexisting melt. To reduce compositional effects, only clinopyroxenes belonging to mildly alkaline (MA) and tholeiitic (TH) series were considered. Pressure was modeled as a linear function of Vcell, VM1, and Mg/(Mg + Fe2+)Cpx ratio. A calibration based on the whole data set (MA + TH) reproduced the experimental pressures within 1.4 kbar at the 1-σ level. The maximum residuals were 3.5 kbar and 3.9 kbar for MA- and TH-clinopyroxenes, respectively. Better statistics were obtained by considering MA- and TH-clinopyroxenes separately. A calibration based on the 69 MA-clinopyroxenes reproduced the experimental pressures within 1.1 kbar (1σ) and with a maximum residual of 2.7 kbar. A calibration based on the 143 TH-clinopyroxenes reproduced the experimental pressures within 1.0 kbar (1σ) and with a maximum residual of 3.4 kbar. When these geobarometers are applied to natural samples for which P is unknown, the correction for compressibility is necessarily made through a trial-and-error procedure. This expedient propagates an additional error that increases the above uncertainties and residuals by a factor of about 2. Applications to natural, igneous rocks for which the pressures of crystallization could be constrained based on experimental, petrological or geological evidence yielded pressure estimates that reproduced the expected values to within ca. 2 kbar. Compared to the MA-formulation, the TH-formulation appears to be less robust to variations in magma composition. When applied to high-pressure (>10 kbar) clinopyroxenes synthesized from very low Na (Na2O < 1.5%) melts, the latter geobarometer can underestimate P by as much as 6 kbar. Calculation of P through the present geobarometers requires clinopyroxene major-element composition and an independent, accurate estimate of crystallization T. Underestimating T by 20 °C propagates into a 1-kbar increase in calculated P. The proposed geobarometers are incorporated in the CpxBar software program, which is designed to retrieve the pressure of crystallization from a clinopyroxene chemical analysis. Received: 11 June 1998 / Accepted: 12 November 1998  相似文献   

11.
The Bleikvassli massive sulfide ore deposit is hosted by Proterozoic pelitic, quartzofeldspathic, and amphibolitic rocks of the Uppermost Allochthon of the Scandinavian Caledonides. Staurolite-garnet-biotite and kyanite-staurolite-biotite assemblages indicate that metamorphism reached the kyanite zone of the amphibolite facies. Geothermobarometry was conducted on rocks in and around the deposit using a variety of silicate and sulfide calibrations. Temperature determinations are most reliant on the garnet-biotite exchange reaction, with analyses obtained from 259 garnet rims and adjacent biotite. Results from nine calibrations of the garnet-biotite geothermometer are considered, but compositional limitations of many calibrations involving high Ca and Mn contents in garnet and AlVI and Ti in biotite make many of the coexisting mineral pairs unsuitable. Average temperatures calculated from the two calibrations that most closely address the garnet-biotite compositions observed at Bleikvassli are 584 °C ± 49 °C and 570 °C ± 40 °C. The application of two calibrations of the garnet-staurolite geothermometer on a limited number of samples yields 581 °C ± 2 °C and 589 °C ± 12 °C, assuming a H2O=0.84, based upon calculations of the modal proportions of gaseous species. Pressure determinations are less constrained. Phengite and plagioclase-biotite-garnet-muscovite geobarometers give average pressures of approximately 5.0 kbar and 8.5 ± 1.2 kbar, respectively. Pressures obtained from the sphalerite-hexagonal pyrrhotite-pyrite barometer average 7.7 ± 1.0 kbar. In consideration of these results, the peak metamorphic conditions at the Bleikvassli deposit are estimated to be 580 °C and 8 kbar. Received: 18 June 1997 / Accepted: 14 May 1998  相似文献   

12.
Calibrations are presented for an independent set of four equilibria between end-members of garnet, hornblende, plagioclase and quartz. Thermodynamic data from a large internally-consistent thermodynamic dataset are used to determine the ΔG° of the equilibria. Then, with the known mixing properties of garnet and plagioclase, the non-ideal mixing in amphibole is derived from a set of 74 natural garnet–amphibole–plagioclase–quartz assemblages crystallised in the range 4–13 kbar and 500–800 °C. The advantage of using known thermodynamic data to calculate ΔG° is that correlated variations of composition with temperature and pressure are not manifested in fictive derived entropies and volumes, but are accounted for with non-ideal mixing terms. The amphibole is modelled using a set of ten independent end-members whose mixing parameters are in good agreement with the small amount of data available in the literature. The equilibria used to calibrate the amphibole non-ideal mixing reproduce pressures and temperatures with average absolute deviations of 1.1 kbar and 35 °C using an average pressure–temperature approach, and 0.8 kbar with an average pressure approach. The mixing data provide not only a basis for thermobarometry involving additional phases, but also for calculation of phase diagrams in complex amphibole-bearing systems. Received: 8 November 1999 / Accepted: 7 July 2000  相似文献   

13.
 Melting relations on the enstatite−diopside (En, Mg2Si2O6−Di, CaMgSi2O6) join, including the compositions of crystalline phases and melts coexisting along the solidi, were experimentally determined in the pressure range 70–224 kbar with a split-sphere anvil apparatus (USSA-2000). Melting is peritectic in enstatite-rich compositions at 70–124 kbar (1840–2100° C) and eutectic at higher pressures, while the diopside-rich clinopyroxene melts azeotropically at 70–165 kbar and up to 300° C lower temperatures than the eutectic. Orthopyroxene is replaced with enstatite-rich clinopyroxene at 120 kbar and 2090°C. First garnet with 17 mol% Di forms on the solidus at 158 kbar and 2100° C. Two garnets coexist on the solidus at 165–183 kbar and 2100° C, garnet coexists with CaSiO3 perovskite at 183–224 kbar (2100–2230° C) and two coexisting perovskites are stable at higher pressures. The melting curve of diopside was determined at 80–170 kbar; the slope becomes negative at 140 kbar and 2155° C. At 170 kbar and 2100° C, diopside with 96% Di breaks down to garnet with 89% Di and CaSiO3 perovskite. The new data were used to calculate an improved temperature-pressure phase diagram for the CMAS system, which can be useful for estimating the mineralogy of the Earth's upper mantle. Received: 15 October 1994 / Accepted: 15 October 1995  相似文献   

14.
Dehydration melting of tonalites. Part II. Composition of melts and solids   总被引：6，自引：0，他引：6  
 Dehydration melting of tonalitic compositions (phlogopite or biotite-plagioclase-quartz assemblages) is investigated within a temperature range of 700–1000°C and pressure range of 2–15 kbar. The solid reaction products in the case of the phlogopite-plagioclase(An45)-quartz starting material are enstatite, clinopyroxene and potassium feldspar, with amphiboles occurring occasionally. At 12 kbar, zoisite is observed below 800°C, and garnet at 900°C. The reaction products of dehydration melting of the biotite (Ann50)-plagioclase (An45)-quartz assemblage are melt, orthopyroxene, clinopyroxene, amphibole and potassium feldspar. At pressures > 8 kbar and temperatures below 800°C, epidote is also formed. Almandine-rich garnet appears above 10 kbar at temperatures ≥ 750°C. The composition of melts is granitic to granodioritic, hence showing the importance of dehydration melting of tonalites for the formation of granitic melts and granulitic restites at pressure-temperature conditions within the continental crust. The melt compositions plot close to the cotectic line dividing the liquidus surfaces between quartz and potassium feldspar in the haplogranite system at 5 kbar and a H 2O = 1. The composition of the melts changes with the composition of the starting material, temperature and pressure. With increasing temperature, the melt becomes enriched in Al2O3 and FeO+MgO. Potash in the melt is highest just when biotite disappears. The amount of CaO decreases up to 900°C at 5 kbar whereas at higher temperatures it increases as amphibole, clinopyroxene and more An-component dissolve in the melt. The Na2O content of the melt increases slightly with increase in temperature. The composition of the melt at temperatures > 900°C approaches that of the starting assemblage. The melt fraction varies with composition and proportion of hydrous phases in the starting composition as well as temperature and pressure. With increasing modal biotite from 20 to 30 wt%, the melt proportion increases from 19.8 to 22.3 vol.% (850°C and 5 kbar). With increasing temperature from 800 to 950°C (at 5 kbar), the increase in melt fraction is from 11 to 25.8 vol.%. The effect of pressure on the melt fraction is observed to be relatively small and the melt proportion in the same assemblage decreases at 850°C from 19.8 vol.% at 5 kbar to 15.3 vol.% at 15 kbar. Selected experiments were reversed at 2 and 5 kbar to demonstrate that near equilibrium compositions were obtained in runs of longer duration. Received: 27 December 1995 / Accepted: 7 May 1996  相似文献   

15.
Trace element distribution in Central Dabie eclogites   总被引：16，自引：0，他引：16  
Coesite-bearing eclogites from Dabieshan (central China) have been studied by ion microprobe to provide information on trace element distributions in meta-basaltic mineral assemblages during high-pressure metamorphism. The primary mineralogy (eclogite facies) appears to have been garnet and omphacite, usually with coesite, phengite and dolomite, together with high-alumina titanite or rutile, or both titanite and rutile; kyanite also occurs occasionally as an apparently primary phase. It is probable that there was some development of quartz, epidote and apatite whilst the rock remained in the eclogite facies. A later amphibolite facies overprint led to partial replacement of some minerals and particularly symplectitic development after omphacite. They vary from very fine-grained dusty-looking to coarser grained Am + Di + Pl symplectites. The eclogite facies minerals show consistent trace element compositions and partition coefficients indicative of mutual equilibrium. Titanite, epidote and apatite all show high concentrations of REE relative to clinopyroxene. The compositions of secondary (amphibolite facies) minerals are clearly controlled by local rather than whole-rock equilibrium, with the composition of amphibole in particular depending on whether it is replacing clinopyroxene or garnet. REE partition coefficients for Cpx/Grt show a dependence on the Ca content of the host phases, with D REE Cpx/Grt decreasing with decreasing D Ca . This behaviour is very similar to that seen in mantle eclogites, despite differences in estimated temperatures of formation of 650–850 °C (Dabieshan) and 1000–1200 °C (mantle eclogites). With the exception of HREE in garnet, trace elements in the eclogites are strongly distributed in favour of minor or accessory phases. In particular, titanite and rutile strongly concentrate Nb and Zr, whilst LREE–MREE go largely into epidote, titanite and apatite. If these minor/accessory minerals behave in a refractory manner during melting or fluid mobilisation events and do not contribute to the melt/fluid, then the resultant melts and fluids will be strongly depleted in LREE–MREE. Received: 11 February 1999 / Accepted: 31 January 2000  相似文献   

16.
More than 99% of mineral inclusions in diamonds from the River Ranch pipe in the Late Archean Limpopo Mobile Belt (Zimbabwe), are phases of harzburgitic paragenesis, namely olivine (Fo92–93), orthopyroxene (Mg# = 93), G10 garnets and chromites. The diamond inclusion (DI) chemistry demonstrates a limited overlap with River Ranch kimberlite macrocrysts: the DI garnets are more Ca-undersaturated, and DI spinel and garnet are more Mg-rich. Most River Ranch diamond inclusions were equilibrated at T = 1080–1320 °C, P = 47–61 kbar, and f O2 between IW and WM buffers. The P/T profile beneath the Limpopo Mobile Belt (LMB) is consistent with a paleo-heat flow of 41–42 mW/m2, similar to calculations for Roberts Victor, but hotter than for the Finsch, Kimberley, Koffiefontein and Premier Mines. This is ascribed to the younger tectonothermal age of the LMB and its proximity to Late Archean oceans. Like diamond inclusions from all other kimberlites studied, the River Ranch DI have a lithospheric affinity and therefore indicate that an ancient, chemically depleted, thick (at least 200 km) mantle root existed beneath the Limpopo Mobile Belt 530–540 Ma ago. The mantle root might have developed beneath the continental Central Zone of the LMB as early as the Archean, and could be alien to the overthrust allochthonous sheet of the Limpopo Belt. Oxygen fugacity estimates for diamond inclusions at River Ranch are similar to other diamondiferous harzburgites beneath the Kaapvaal craton, indicating that the Kaapvaal mantle as a whole was well buffered and homogeneous with respect to f O2 at the time of peridotitic diamond crystallization. Received: 11 January 1995 / Accepted: 10 June 1997  相似文献   

17.
 The interpretation of metamorphically induced U-Pb isotopic discordance requires a thorough understanding of zircon-fluid interactions. With this aim we have studied the behaviour of metamict and crystalline zircon phases and their U-Pb systems by cathodoluminescence after treatment by 2M Na2CO3 solution at T = 200–800 °C and P = 1–5 kbar for 3–14 days, X-ray diffraction, microprobe and isotope dilution analysis. The data indicate that zircon transformation under hydrothermal conditions depends on the experimental conditions and the degree of structural damage. Reconstitution of defective and impurity-enriched zones of metamict zircon (homogenization of impure element concentrations and increase of crystallinity) was observed at 400 °C and P = 1 kbar. Considerable lead and uranium loss occurred under these conditions. As a result of zircon dissolution, newly formed baddeleyite accommodating U from 2M Na2CO3 solution and Zr-Na-silicate were recognized. This process intensified with increasing pressure. Study of crystalline zircon indicates that migration of U and Pb took place only during dissolution of zircon at T above 650 °C. In the presence of carbonate-ions essential U and Pb amounts are lost from metamict zircon at a lower P-T than is typical for greenschist facies metamorphism. Received: 4 October 1997 / Accepted: 6 December 1999  相似文献   

18.
 Picritic units of the Miocene shield volcanics on Gran Canaria, Canary Islands, contain olivine and clinopyroxene phenocrysts with abundant primary melt, crystal and fluid inclusions. Composition and crystallization conditions of primary magmas in equilibrium with olivine Fo90-92 were inferred from high-temperature microthermometric quench experiments, low-temperature microthermometry of fluid inclusions and simulation of the reverse path of olivine fractional crystallization based on major element composition of melt inclusions. Primary magmas parental for the Miocene shield basalts range from transitional to alkaline picrites (14.7–19.3 wt% MgO, 43.2–45.7 wt% SiO2). Crystallization of these primary magmas is believed to have occurred over the temperature range 1490–1150° C at pressures ≈5 kbar producing olivine of Fo80.6-90.2, high-Ti chrome spinel [Mg/ (Mg+Fe2+)=0.32–0.56, Cr/(Cr+Al)=0.50–0.78, 2.52–8.58 wt% TiO2], and clinopyroxene [Mg/(Mg+Fe)=0.79–0.88, Wo44.1-45.3, En43.9-48.0, Fs6.8-11.0] which appeared on the liquidus together with olivine≈Fo86. Redox conditions evolved from intermediate between the QFM and WM buffers to late-stage conditions of NNO+1 to NNO+2. The primary magmas crystallized in the presence of an essentially pure CO2 fluid. The primary magmas originated at pressures >30 kbar and temperatures of 1500–1600° C, assuming equilibrium with mantle peridotite. This implies melting of the mantle source at a depth of ≈100 km within the garnet stability field followed by migration of melts into magma reservoirs located at the boundary between the upper mantle and lower crust. The temperatures and pressures of primary magma generation suggest that the Canarian plume originated in the lower mantle at depth ≈900 km that supports the plume concept of origin of the Canary Islands. Received: 23 October 1995/Accepted: 21 February 1996  相似文献   

19.
Summary In the Kutná Hora Complex, the Běstvina Formation, which is similar to Gf?hl granulite, contains eclogite that has escaped widespread retrograde recrystallization. The eclogite assemblage, garnet + omphacite + quartz + rutile ± plagioclase, yields an estimate for peak metamorphic conditions of 18–20 kbar and 835–935 °C, which is comparable to that determined from felsic granulite, 14–20 kbar and 900–1000 °C. Garnet in eclogite exhibits both prograde and retrograde compositional zoning, from which constraints on thermal history of the Gf?hl terrane can be derived by diffusion modelling. At 900 °C, a garnet grain of 800–1000 μm radius would homogenize in 7.5–11.7 million years, but the existence of compositional gradients on a length scale of 100–200 μm suggests that the duration of peak metamorphism may have been limited to ∼500,000 years. Diffusion modelling of retrograde zoning in garnet yields a cooling rate of 150–100 °C/m.y. for a radius of 800–1000 μm and initial temperature of 900 °C. The relatively brief duration of high-pressure/high-temperature metamorphism and rapid cooling and exhumation of the Gf?hl terrane may be a consequence of lithospheric delamination during Early Carboniferous collision of Bohemia (Teplá-Barrandia) and Moldanubia (Franke, 2000).  相似文献   

20.
The expansivity of supercooled diopside liquid has been determined using techniques of container-based dilatometry. Two thermal strategies have been employed, one in which the sample is brought to volumetric equilibrium by long-duration dwells at low temperatures (817 °C) and one in which scanning dilatometry of the sample has been performed at somewhat higher temperatures (890–913 °C). The results of both experiments yield a supercooled liquid expansivity for diopside liquid in the temperature range of 817–913 °C of 84.4 ± 2.8 × 10−4 cm3/mol K. The expansivity is 65% higher than that obtained for diopside melt obtained at superliquidus temperatures using the double bob Archimedean method. Combined fitting of the new low temperature, volume–temperature data from the present study and the superliquidus data from the literature has been performed. The combined fit yields the following equations for the volume–temperature relationship of diopside liquid (T=temperature in °C):
The standard error of the fit using both equations reproduces the volume–temperature data for diopside liquid within experimental error. This result reconciles the disparate values of expansivity measured at low temperatures in the supercooled state and at superliquidus temperatures and confirms the temperature-dependence of the expansivity of diopside liquid. Comparison with previous low temperature estimates of melt volume and expansivity are discussed in light of these new results. Received: 18 November 1999 / Accepted: 24 January 2000  相似文献   

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