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1.
Adopting a set of multioxide components and using published compositional data on olivineand plagioclase-liquid equilibria we have developed a 17 component regular solution model for met-aluminous silicate liquids. The partial molar excess free energies predicted from this model can be used together with phenocryst compositions as an effective geothermometer, with an approximate error of 20 °C (30 °C for olivine, 12 °C for plagioclase). The regular solution formulation is also successful in predicting liquid immiscibility at (1) high mole fractions of silica commonly observed in phase diagrams, and at (2) lower temperatures in lunar basalts and intermediate lavas. The model yields activities of silica which are consistent with those obtained from solid-liquid silica buffers in rocks which contain olivine and enstatite or quartz. From predicted activities of KAlSi3O8 in liquids coexisting with plagioclase a value is obtained for the limiting Henry's law activity coefficient of KAlSi3O8 in the solid. This coefficient agrees well with that inferred from plagioclase-sanidine equilibrium phenocryst assemblages in rhyolites. The activities of silica obtained from this model are used to place constraints on the pressure-temperature regions where various types of basic magmas are generated. In conjunction with plagioclase geothermometry an application is given where the pressure, temperature, and water content of an olivine andesite is predicted from the activity of silica.  相似文献   

2.
Experimental Petrology of Melilite Nephelinites   总被引：3，自引：1，他引：3  
Experimental study of natural melilite nephelinite lavas ofintermediate K/Na ratio at low pressure (fo2 reveals the presenceof a peritectic ‘point’ of distributary type (1090?C)for liquids saturated with leucite, nepheline, and spinel. Withdecreasing temperature on the olivine + melilite cotectic, botholivine and melilite react with such liquids to produce high-calciumpyroxene at the peritectic. Both the olivine + high-calciumpyroxene and melilite + high-calcium pyroxene cotectics arestable at temperatures below the peritectic. Olivines coexistingwith such liquids are much more magnesian than those in comparabletholeiitic liquids. The olivine-liquid Fe-Mg distribution coefficient is a monotonically increasing function of silica activity over the composition range spannedby melilite nephelinite, ugandite, alkali basalt, and tholeiitebasalt liquids. The analogous Fe-Mg distribution coefficientfor melilite and liquid is effectively constant , while that for high-calcium pyroxene and liquidis highly dependent on the chemistry of high-calcium pyroxene(cf., Sack & Carmichael, 1984). Pseudoternary liquidus projectionsof multiply saturated liquids coexisting with nepheline, leucite,and spinel (?olivine?high-calcium pyroxene?melilite) have beenprepared to facilitate graphical analysis of the evolution oflava compositions during hypabyssal cooling. Major element chemicalanalyses and petrographic features of lavas from Mt. Nyiragongo,East Africa and Oahu, Hawaii (e.g., Denaeyer et al., 1965; Wilkinson& Stolz, 1983) confirm the validity of these diagrams andthe systematics established from the experimental data. *Reprint requests to R.O. Sack  相似文献   

3.
A thermodynamic model for the Gibbs free energy of igneous pyroxenes with the general formula [Na, Ca, Fe2+, Mg]M2[Fe2+, Mg, Ti, Al, Fe3+]M1[Al, Fe3+, Si]TetSiO6 is calibrated from experimentally determined compositions of coexisting pyroxene and silicate melt. The model is based upon the general formulation, and relies upon the calibration of the “quadrilateral” subsystem, previously published by the present authors. The calibration database of pyroxene-liquid equilibria spans a broad spectrum of temperature, pressure and oxygen fugacity conditions, ranging from 1000°–1600°C, 0.001–30 kbar and iron-wüstite to air. Chemical potentials of endmember pyroxene components as well as exchange potentials between pyroxenes and coexisting liquids are defined utilizing the present authors' thermodynamic melt model. Model parameters are extracted from these relations by regression analysis. The resulting model and derivative endmember properties are internally consistent with an existing standard state thermodynamic database. The success of the model and its applicability to igneous petrogenesis are demonstrated by comparing calculated and experimentally determined liquidus compositions, temperatures and symmetry states for pyroxenes crystallizing from a variety of silicate melts, ranging in composition from tholeiites and angrites through rhyolites to potash ankaratrites.  相似文献   

4.
We report results of anhydrous 1 atm and piston-cylinder experiments on ID16, an Aleutian high-magnesia basalt (HMB), designed to investigate potential petrogenetic links between arc high-alumina basalts (HABs) and less common HMBs. ID16 is multiply saturated with a plagioclase/spinel iherzolite mineral assemblage (olivine, plagioclase, clinopyroxene, orthopyroxene, spinel) immediately beneath the 12 kbar liquidus. Derivative liquids produced at high temperatures in the 10–20 kbar melting interval of ID16 have compositions resembling those published of many moderate-CaO HABs, although lower-temperature liquids are poorer in CaO and richer in alkalies than are typical HABs. Isomolar pseudoternary projections and numerical mass-balance modeling suggest that derivative melts of ID16 enter into a complex reaction relationship with olivine at 10 kbar and 1,200° C–1,150° C. We sought to test such a mechanism to explain the lack of liquidus olivine in anhydrous experiments on mafic high-alumina basalts such as SSS. 1.4 (Johnston 1986). These derivative liquids, however, do not resemble typical arc high-alumina basalts, suggesting that olivine-liquid reaction does not account for Johnston's (1986) observations. Instead, we suggest that olivine can be brought onto the liquidus of such compositions only through the involvement of H2O, which will affect the influence of bulk CaO, MgO, and Al2O3 contents on the identity of HAB liquidus phases (olivine or plagioclase) at pressures less than 12 kbar.  相似文献   

5.
P. Thy 《Lithos》1991,26(3-4):223-243
Melting experiments have been performed on a primitive, mildly alkalic glassy lava (10 wt.% MgO) from the 1965 eruption of the Surtsey volcano located at the tip of the south-eastern propagating rift zone of Iceland. At atmospheric pressure, approximately on the FMQ oxygen buffer, olivine (Fo81) crystallizes from 1240°C, followed by plagioclase (An70) from 1180°C and augite from 1140°C. The experimental glasses coexisting with olivine, plagioclase and augite are ferrobasaltic enriched in FeO (13.6–14.2 wt.%) and TiO2 (4.0–4.4 wt.%). In high pressure, piston-cylinder, graphite-controlled runs, olivine occurs as the liquidus phase until 14 kbar, above which augite is the liquidus phase. Low-Ca pyroxene is not a liquidus phase at any pressure. The high pressure liquids are, relative to the one atmosphere liquids, significantly enriched in Al2O3 and Na2O and depleted in CaO as a result of changes in the crystallizing assemblages. Furthermore, liquidus augite is dominantly subcalcic and shows significant enrichment in Al and depletion in Ti. Subliquidus plagioclase is enriched in sodium relative to low pressure phase compositions. Evaluated in normative projections, contrasting liquid lines of descent are revealed as a function of pressure. At one atmosphere, the multisaturated liquids are located close to the thermal divide defined by the plane olivine-plagioclase-augite, but appear, with advanced degrees of crystallization, to be moving away from the thermal divide toward normative quartz. The augites crystallizing in the one atmosphere experiments are calcic and slightly nepheline normative. In the 10 and 12.5 kbar experiments, the augites become subcalcic and dominantly hypersthene normative. Because of this shift in augite compositions, transitional basaltic liquids may at high pressure evolve from the tholeiitic side of the olivine-plagioclase-diopside normative divide onto the alkalic side. With increasing pressure above 15 kbar, the liquidus augite compositions move back toward the olivine-plagioclase-diopside normative divide.  相似文献   

6.
Experiments in the system high-A1 basalt (HAB)-water have been conducted in the melting range at pressures between 1 atm. and 10 kbar, defining the amphibole stability field and the composition of liquids which coexist with this amphibole. Plagioclase is the anhydrous liquidus phase between 1 atm. and 10 kbar but in the hydrous runs this role is taken by olivine at <7 kbar and then by clinopyroxene at higher pressures. Because amphibole is never on the high-A1 basalt liquidus it is not likely that andesite is derived from primary basalt by pure fractional crystallisation, although as we discuss, other mechanisms including equilibrium crystallisation might implicate amphibole. If primary basaltic magma undergoes closed-system equilibrium crystallisation, then the amphibole field will be intersected at between 50 and 100°C below the liquidus. The compositions of melts coexisting with amphibole alone do not match those of any of the natural andesite or dacitic lavas associated with the particular high-A1 basalt investigated. Like natural andesites, they become rapidly silica enriched, but they also become far more depleted in TiO2 and MgO. However, the compositions of liquids lying directly on the divariant amphibole-out reaction zone, where amphibole +liquid coexist with clinopyroxene or olivine (±plagioclase), do resemble those of naturally occurring low-silica andesites. With increasing temperature pargasitic amphibole breaks down via incongruent melting reactions over a narrow temperature range to form a large volume of relatively low-silica basaltic andesite liquid and a crystalline assemblage dominated by either clinopyroxene or olivine. Our important conclusion is that basaltic andesite liquid will be the product of reaction between cooling, hydrous mafic liquid and anhydrous ferromagnesian phases. The solid reactants could represent earlier cumulates from the same or different magma batches, or they could be peridotite wall-rock material. Because the amphibole-out boundary coexisting with liquid is one of reaction, it will not be traversed so long as the phases on the high temperature side remain. Thus, the assemblage amphibole+clinopyroxene±olivine±plagioclase+liquid is one in which the liquid is buffered (within limits), and results reported here indicate that this buffering generates melts of low-silica andesite composition. When tapped to lower pressures these liquids will rise, eventually to fractionate plagioclase-rich assemblages yielding silicarich andesite and dacite melts. Conversely, the partial melting of hornblende pyroxenite, hornblende peridotite or hornblende gabbro can also yield basaltic andesite liquids. The phase relationships suggested by these experiments are discussed in the light of naturally occurring phenocryst and xenolith assemblages from the east Sunda Arc. Primary magmatic additions to the lithosphere of volcanic arcs are basaltic and voluminous upper crustal andesite in these terranes, complemented by mafic and ultramafic crystalline deposits emplaced in the lower crust or close to the Moho. Together these components constitute total arc growth with a basaltic composition and represent the net accreted contribution to continental growth.  相似文献   

7.
The Howqua Olivine Pyroxenite of eastern Victoria, Australia, intrudes a metamorphosed sequence of Cambrian high-Mg lavas. It crystallized an unusual mineral assemblage: Cr-rich magnesiochromite, olivine (Fo94), and protoenstatite (now inverted to polysynthetically-twinned clinoenstatite). Residual liquid crystallized strongly-zoned interstitial pyroxenes followed by pargasite. Pargasite, often showing quench habit, crystallized in interstitial glass which is now altered to serpentine.The extremely refractory nature of the cumulus phases indicates a very high temperature of crystallization for liquidus olivine and chromite from a high-MgO, low-Al2O3 parent liquid similar in some respects to Archaean peridotitic komatiites. The suggested origin by hydrous melting of depleted mantle peridotite, plus other compositional and mineralogical similarities (especially the olivine-liquid reaction producing protoenstatite) indicate that the parent magma of the Howqua Olivine Pyroxenite had many features in common with the high-SiO2, high-MgO clinoenstatite-bearing boninitic lavas of the Western Pacific. It is interpreted as a more extreme melt with affinities to boninite and it demonstrates that ultramafic magmas existed in the Cambrian.  相似文献   

8.
Basaltic liquids, saturated at one-atmosphere in augite, olivine, and plagioclase, show a strong linear trend in pseudo-quaternary projections from nepheline to slightly quartz normative compositions. Coexisting augites show a corresponding variation from slightly nepheline to hypersthene normative compositions. Consequently, alkalic and mildly alkalic liquids coexist with nepheline normative augites; tholeiitic liquids coexist with hypersthene normative augites; and transitional liquids coexist with augites compositionally intermediate between those crystallizing in alkalic and tholeciitic melts. The variation in augite composition is due to a decrease in wollastonite and non-quadrilateral components, going from mildly alkalic, to transitional, and tholeiitic augites. The observed liquid and augite trends lack correlations between normative composition and crstallization temperature. This is an artifact of plotting unrelated liquid lines of descent. Individual liquid lines of descent, in contrast, display good correlation between normative composition and crystllization temperature, which, for both liquids and coexisting augites, are highly oblique to nearly perpendicular to the general trend. Because the composition of the first augite to appear on the liquidus varies as a function of the bulk system, the location of the thermal divide shows corresponding variations. As a consequence, unifying cotectics and pseudo-quaternary normative projections should not, without specific experimental knowledge, be used to address liquid lines of descent and common magmatic parentages.  相似文献   

9.
Activity/composition relations in the ternary feldspars   总被引：6，自引：0，他引：6  
Activity/composition relations are presented for high-structural state feldspars whose bulk compositions lie within the ternary system NaAlSi3O8 CaAl2Si2O8-KAlSi3O8. The expressions are parameterized from the data for coexisting feldspars of Seck (1971a) using an asymmetric regular solution approximation for the excess Gibbs free energy of mixing and an Al-avoidance model for the configurational entropy of solution. The solution properties of the plagioclase and alkali-feldspar binaries have been made to conform to the recent work of Thompson and Hovis (1979) and Newton et al. (1980). Using the proposed model the ternary feldspar solvus is extrapolated in temperature (up to 1,500° C) and pressure (up to 5kbars). A new two-feldspar geothermometer is presented which provides somewhat more reasonable estimates of crystallization temperatures than the equations and graphs of Stornier (1975), Powell and Powell (1977), Brown and Parsons (1981) and Haselton et al. (1983). In conjunction, some criteria are suggested for establishing the existence of equilibrium tie-lines between coexisting ternary feldspars in rhyolites and trachytes. Calculated values of the activity of KAlSi3O8 in plagioclase are examined in some detail. These compare favorably with independent estimates obtained from experimentally grown plagioclases precipitating at liquidus temperatures from igneous rocks of widely varying alkali contents.  相似文献   

10.
A major question concerning the Bushveld Complex is the relationship between the layered mafic rocks and the overlying Rooiberg Group felsites and related granophyres. Here, we assemble bulk-rock analyses to gain insight into this question and investigate the petrogenesis of the felsic rocks. The data indicate that the Rooiberg Group consists of distinctive magnesian and ferroan lavas. The former dominates the basalts to rhyolites of the basal Dullstroom Formation, while nearly all the dacites to rhyolites of the overlying Damwal, Kwaggasnek, and Schrikkloof Formations are ferroan. The ferroan rocks also include the Stavoren Granophyre, which exists regionally as a several-hundred-meter-thick concordant sheet between the Bushveld Complex and Rooiberg lavas. The compositions of the magnesian lavas are similar to calc-alkaline granitoids found in convergent margins, suggesting that the lavas could have originated in a mantle affected by previous Archean subduction events that are recorded by xenoliths and inclusions in diamonds from most Kaapvaal kimberlites. In contrast, the compositions of the ferroan lavas indicate formation by fractional crystallization of basaltic liquids and are essentially identical to ferroan rhyolites associated with mafic rocks from other settings. The hypothesis that these rocks are fractional crystallization products of Bushveld mafic liquids is consistent with published radiogenic and stable isotope data and known age relations. Based on compositional characteristics and geologic relations, the Stavoren Granophyre is the most likely candidate for the residual liquid that escaped from the top of the Bushveld Complex. Whether the bulk of the Bushveld Province ferroan rhyolites formed in the chamber of the extant layered mafic sequence or in a deeper, hidden crustal magma reservoir remains unclear.  相似文献   

11.
The Baffin Bay picrites have been the focal point of a controversy concerning the MgO content of primary magmas derived from the upper mantle. A sample population of 48 lava chilled margins collected across the Baffin Bay volcanic succession at the northeastern tip of Padloping Island exhibits a prominent compositional mode between 14 and 16 weight percent MgO (19–22 Mg, cation units = Mg/100 cations). The petrography of these samples, however, requires that the Padloping magmas were mixtures of olivine crystals and liquid at their eruption. Olivine phenocrysts constituted 15 to 30 volume percent of these magmas and retain compositions requiring coexisting liquid compositions with only 10 to 13.5 weight percent MgO (14–18.5 Mg). However, highly magnesian, olivine xenocrysts (up to Fo 93) found in the most magnesian lavas require the former existence of liquids with at least 18 weight percent MgO (24 Mg). If these xenocrysts represent early cumulates, then the primary liquids of the Padloping suite must have been at least this MgO rich with temperatures greater than 1,425° C. Such primary liquids could have evolved by olivine crystallization to a steady state, equilibrated crystal — liquid mixtures in a shallow reservoir system prior to eruption. The compositions of the liquids of these mixtures appear to have been perched at the point of plagioclase saturation at approximately 1,275° C.Despite the complications of mechanical sorting of olivine crystals, the virtual compositional reciprocity of olivine addition and olivine fractionation requires that the bulk compositions of picritic lavas provide compositional analogues of their primary magmas. A comparison of Phanerozoic picrite suites indicates that the Fe contents of terrestrial primary magmas of tholeiitic affinity have a restricted range from 6–9 Fe. Primary magmas associated with intra-plate volcanism appear to be distinctly more Fe-rich than those associated with inter-plate volcanism. The Al/Si ratios of Phanerozoic picrite suites could suggest that the primary magmas of MORB volcanism have equilibrated with relatively Fe-poor source regions at deeper levels in the Earth's mantle than those of other tholeiitic primary magmas.  相似文献   

12.
A thermodynamic model is proposed for calculation of liquidus relations in multicomponent systems of geologic interest. In this formulation of mineral-melt equilibria, reactions are written in terms of the liquid oxide components, and balanced on the stoichiometry of liquidus phases. In order to account for non-ideality in the liquid, a ‘Margules solution’ is derived in a generalized form which can be extended to systems of any number of components and for polynomials of any degree. Equations are presented for calculation of both the excess Gibbs free energy of a solution and the component activity coefficients.Application to the system CaO-Al2O3-SiO2 at one atmosphere pressure is achieved using linear programming. Thermodynamic properties of liquidus minerals and the melt are determined which are consistent with adopted error brackets for available calorimetric and phase equilibrium data. Constraints are derived from liquidus relations, the CaO-SiO2 binary liquid immiscibility gap, solid-solid P-T reactions, and measured standard state entropies, enthalpies, and volumes of minerals in this system.Binary and ternary liquidus diagrams are recalculated by computer programs which trace cotectic boundaries and isothermal sections while checking each point on a curve for metastability. The maximum differences between calculated and experimentally determined invariant points involving stoichiometric minerals are 17°C and 1.5 oxide weight per cent. Because no solid solution models have been incorporated, deviations are larger for invariant points which involve non-stoichiometric minerals.Calculated heats of fusion, silica activities in the melt, and heats of mixing of liquids compare favorably with experimental data, and suggest that this model can be used to supplement the limited amount of available data on melt properties.  相似文献   

13.
Ultramafic inclusions and megacrysts are unusually abundant in a nephelinite sill in the Nandewar Mountains in north-eastern New South Wales. The inclusions are divisible into a Cr-diopside group and a Ti-augite group, the former being dominated by Cr-spinel Iherzolites of restricted modal composition, the latter by olivine and titaniferous Al-rich clinopyroxene assemblages which vary widely in their modal proportions. The principal megacryst species are olivine and black, titaniferous Al-rich clinopyroxene; additional but comparatively rare megacrysts include titanphlogopite, kaersutitic amphibole, and deep green, relatively Fe-rich clinopyroxene. The Cr-spinel Iherzolites conform closely in mineralogy and chemistry with the spinel lherzolites which dominate upper mantle xenolith assemblages in alkaline mafic volcanic rocks from other provinces. Megacrysts and Ti-augite inclusion mineral assemblages are consistently more Fe-rich than analogous phases in the Cr-diopside xenoliths and also display more extensive cryptic variation. The available experimental data on the high pressure liquidus or near-liquidus phases in olivine nephelinite and related compositions indicate that the olivine and black clinopyroxene megacrysts were precipitated at pressures in the vicinity of 15–20 kb. The similarity in the nature and compositions of the principal megacryst species to analogous phases in the Tiaugite group of inclusions indicates that the latter also represent cognate cumulates derived from the olivine nephelinite at broadly comparable pressures. High pressure fractionation of the host olivine nephelinite liquid, controlled mainly by the separation of olivine and aluminous clinopyroxene, produced only comparatively minor compositional changes in the derivative liquid. The hiatus in olivine compositions at approximately Fo86–88, apparently characteristic of the olivines in coexisting Cr-diopside and Ti-augite inclusions, is assessed in terms of the compositions of olivine in equilibrium with alkali basaltic liquids at high pressures.  相似文献   

14.
The activity-composition relations for calcium-rich and calcium-poor amphiboles are calculated from the composition of coexisting cummingtonite-hornblende pairs from a suite of New Zealand rhyolites. The activities are formulated in terms of site occupancies and the regular solution model is used to represent non-ideal mixing of the cations on each site. The regular solution parameters for each site are calculated from the compositions of the coexisting amphiboles. The resulting activity-composition relations are used to calibrate the standard Gibbs energy change for the reaction $${\text{7MgSiO}}_{\text{3}} {\text{ + SiO}}_{\text{2}} {\text{ + H}}_{\text{2}} {\text{O = Mg}}_{\text{7}} {\text{Si}}_{\text{8}} {\text{O}}_{{\text{22}}} {\text{(OH)}}_{\text{2}} $$ assuming that the lowest temperature rhyolites in this suite crystallised at \(P_{{\text{H}}_2 {\text{O}}} = P_{{\text{total}}} \)   相似文献   

15.
An olivine basalt, a tonalite (andesite), a granite (rhyolite), and a red clay (pelagic sediment) were reacted, with known quantities of water in sealed noble metal capsules, in a piston-cylinder apparatus at 30 kb pressure. For the pelagic sediment, with H2O+=7.8% and no additional water, the liquidus temperature is 1240°C, the primary phases are garnet and kyanite. The subsolidus phase assemblage is phengite mica+garnet+clinopyroxene+coesite+kyanite. With 5 wt.% water added, the liquidus temperatures and primary phases for the calc-alkaline rocks are 1280°-1180°-1080°, garnet+clinopyroxene, garnet, and quartz respectively. Garnet and clinopyroxene occur throughout the melting interval of the olivine tholeiite for all water contents. Garnet is joined by clinopyroxene 80° below the andesite plus 5% H2O liquidus, quartz is joined by clinopyroxene 180° below the rhyolite plus 5% H2O liquidus. The subsolidus phase assemblage is garnet+clinopyroxene+coesite+minor kyanite for all the calc-alkaline compositions. We conclude that calc-alkaline andesites and rhyolites are not equilibrium partial melting pruducts of subducted oceanic crust consisting of olivine tholeiite basalt and siliceous sediments. Partial melting in subduction zones produces broadly acid and intermediate liquids, but these liquids lie off the calc-alkaline basalt-andesite-rhyolite join and must undergo modification at lower pressures to produce calcalkaline magmas erupted in overlying island arcs.  相似文献   

16.
 Thermodynamic analysis of Fe- and Mg-bearing plagioclase and silicate liquid was carried out based on reported element partitioning data between plagioclase and silicate liquid in reduced conditions, solution properties of ternary feldspar, standard state properties of plagioclase endmembers and solution properties of multicomponent silicate liquid. Derived mixing properties of Fe- and Mg-bearing plagioclase are in harmony with estimated results from synthetic experiments in the systems CaAl2Si2O8-CaFeSi3O8 and CaAl2Si2O8-CaMgSi3O8. Based on the determined solution properties of the plagioclase, a computer program to calculate the element partition relationships between Fe- and Mg-bearing plagioclase and multicomponent silicate liquid was developed. The FeO, MgO and MgO/(MgO + FeO) in plagioclase predicted from known liquid compositions and pressure are in agreement with measurements within 0.2 wt%, 0.1 wt% and 0.1 (mol ratio), respectively. The Fe3+ content in plagioclase crystallized at high oxygen fugacity can be estimated with this program. The Fe3+/total Fe ratio in plagioclase crystallized near the quartz-fayalite-magnetite buffer ranges from 0 to 0.5, which is consistent with previous study on natural plagioclase in submarine basalt. Derived solution properties of the Fe- and Mg-bearing plagioclase are also used to calculate equilibrium composition relationship between olivine and plagioclase. Change of X Fo in olivine coexisting with plagioclase affects MgO and FeO contents in plagioclase greatly. The present model predicts X Fo of coexisting olivine from the chemical composition of plagioclase to ±0.1 accuracy at given pressure and temperature. Received: 27 March 1998 / Accepted: 30 September 1999  相似文献   

17.
Lavas from Medicine Lake volcano, Northern California have been examined for evidence of magma mixing. Mixing of magmas has produced basaltic andesite, andesite, dacite and rhyolite lavas at the volcano. We are able to identify the compositional characteristics of the components that were mixed and to estimate the time lag between the mixing event and eruption of the mixed magma. Compositional data from pairs of phenocrysts identify a high alumina basalt (HAB) and a silicic rhyolite as endmembers of mixing. Mg-rich olivine or augite and Ca-rich plagioclase are associated with the HAB component, and Fe-rich orthopyroxene and Na-rich plagioclase are associated with the rhyolitic component. Some lavas contain multiple phenocryst assemblages suggesting the incorporation of several magmas intermediate between the HAB and silicic components. Glass inclusions trapped in Mg-rich olivine and Na-rich plagioclase are similar in composition to the proposed HAB and rhyolite end members and provide supportive evidence for mixing. Textural criteria are also consistent with magma mixing. Thermal curvature of the liquidus surfaces in the basalt-andesite-rhyolite system allows magmas produced by mixing to be either supercooled or superheated. Intergranular textures of basaltic andesites and andesites result from cooling initiated below the liquidus. The trachytic textures of silicic andesites form from cooling initiated above the liquidus. Reversed compositional zoning profiles in olivine crystals were produced by the mixing event, and the homogenization of the compositional zoning has been used to estimate the time interval between magma mixing and eruption. Time estimates are on the order of 80 to 90 h, suggesting that the mixing event triggered eruption.  相似文献   

18.
The Saurashtra region in the northwestern Deccan continental flood basalt province (India) is notable for compositionally diverse volcano-plutonic complexes and abundant rhyolites and granophyres. A lava flow sequence of rhyolite-pitchstone-basaltic andesite is exposed in Osham Hill in western Saurashtra. The Osham silicic lavas are Ba-poor and with intermediate Zr contents compared to other Deccan rhyolites. The Osham silicic lavas are enriched in the light rare earth elements, and have εNd (t = 65 Ma) values between −3.1 and −6.5 and initial 87Sr/86Sr ratios of 0.70709-0.70927. The Osham basaltic andesites have initial εNd values between +2.2 and −1.3, and initial 87Sr/86Sr ratios of 0.70729-0.70887. Large-ion-lithophile element concentrations and Sr isotopic ratios may have been affected somewhat by weathering; notably, the Sr isotopic ratios of the silicic and mafic rocks overlap. However, the Nd isotopic data indicate that the silicic lavas are significantly more contaminated by continental lithosphere than the mafic lavas. We suggest that the Osham basaltic andesites were derived by olivine gabbro fractionation from low-Ti picritic rocks of the type found throughout Saurashtra. The isotopic compositions, and the similar Al2O3 contents of the Osham silicic and mafic lavas, rule out an origin of the silicic lavas by fractional crystallization of mafic liquids, with or without crustal assimilation. As previously proposed for some Icelandic rhyolites, and supported here by MELTS modelling, the Osham silicic lavas may have been derived by partial melting of hot mafic intrusions emplaced at various crustal depths, due to heating by repetitively injected basalts. The absence of mixing or mingling between the rhyolitic and basaltic andesite lavas of Osham Hill suggests that they reached the surface via separate pathways.  相似文献   

19.
Magmatic Ni-Cu-PGE sulfide mineralization occurs within olivine clinopyroxenite, hornblende-bearing clinopyroxenite, and magnetite-hornblende-rich rocks in the Ural-Alaskan-Type Duke Island Complex in Southeast Alaska. The addition of large amounts of sulfur from country rocks occurred during fractional crystallization of the parental magma when clinopyroxene was becoming a liquidus mineral. Textural interfaces between sulfide and silicate minerals are strongly interlobate, and differ significantly from net-textures that are developed in many Ni-Cu-PGE deposits. Sulfide-free olivine clinopyroxenite is an adcumulate; residual liquid was efficiently expelled from the accumulating crystal pile. A significant interstitial liquid component is observable only in the form of interstitial sulfide in the S-rich rocks. Rounded sulfide inclusions and blebby to vermicular sulfide-silicate intergrowths indicate that silicate crystallization occurred under conditions of sulfide saturation. The presence of dense sulfide liquid inhibited the growth of silicate minerals and led to the development of interlobate grain boundaries. Strong, localized wetting of sulfide liquids on crystallizing silicates, and downward percolation of sulfide liquid through a crystallizing mush may have contributed to the evolution of these textures. Residual silicate liquid was removed from the system due to a combination of buoyant advection and compaction, but dense sulfide liquid remained.  相似文献   

20.
Pressure-temperature conditions for which “andesitic” liquids (～60% SiO2) may coexist with mineral assemblages of the type magnesian olivine + orthopyroxene + clinopyroxene±amphibole±phlogopite have been investigated, both by means of partial melting experiments on the pyrolite model composition, and by experiments involving addition of olivine to andesite or basaltic andesite compositions at or near their liquidus temperatures. In the latter experiments, reaction relationships between quartz-normative liquid and olivine were made to proceed until olivine persisted. The composition of the final liquid in equilibrium with olivine (plus pyroxenes etc.) was then estimated by microprobe analysis of its quench products (glass, quench crystals). The inferred liquid compositions were tested for equilibrium with coexisting crystals using criteria based on mass balance within the total assemblage, equilibrium element partition relationships, and the requirement that the liquidus temperatures and near-liquidus crystalline phases of these compositions should closely match the temperature of the original olivine-addition experiment and the crystalline phases developed during it. At 1000° C–1050° C, liquids which satisfy these criteria for equilibrium with assemblages which include olivine are “andesitic” (58–60% SiO2, 5–12% normative Qz) only at water pressures ≤ 10kb. At 15 kb, liquids in equilibrium with olivine at 1000° C and 980° C have ～56% SiO2, high alkali contents, and 5–10% normative olivine. Similar compositions are in equilibrium with orthopyroxene and garnet alone at 20 kb. These results show that andesitic magmas are unlikely to be produced by melting of a peridotitic mantle at pressures >10 kb (depths>35 km). If hydrous, but otherwise geochemically primitive peridotitic compositions are partially melted at pressures<10 kb, then “andesitic” products will be much more magnesian and poorer in alkalies than typical natural andesites. These conclusions raise serious difficulties for models of andesite genesis by the melting of hydrous peridotitic mantle immediately overlying Benioff zones.  相似文献   

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