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1.
Layered sills and flows are conspicuous in the komatiitic volcanics of the Chukotat Group of the Aphebian Cape Smith fold belt in New Quebec. These bodies consist of a lower ultramafic member with an overlying gabbroic complex and are bound by margins of quench-textured, pyroxene-rich melanogabbro. Features such as cyclic layering of pyroxenite and peridotite, successive appearance of euhedral olivine, clinopyroxene, and plagioclase, and polarized compositional variation indicate that the ultramafic member and lower gabbro are crystal cumulates. The uppermost gabbros, however, appear to represent liquids derived by removal of these cumulates. The significance of these bodies is that their initial liquids were at least as basic as pyroxenitic komatiites (14 wt.% MgO) while the residual liquids are Fe-Ti-rich tholeiites. Similarity between the liquid line of descent within these differentiated bodies and the spectrum of volcanic composition of the Chukotat Group as a whole suggests that the komatiites and tholeiites of the latter may constitute a single magmatic suite whose chemical diversity is a function of low-pressure, crystal fractionation.  相似文献   

2.
A new version of COMAGMAT-3.5 model designed for computer simulations of equilibrium and fractional crystallization of basaltic magmas at low to high pressures is presented. The most important modifications of COMAGMAT include an ability to calculate more accurately the crystallization of magnetite and ilmenite, allowing the user to study numerically the effect of oxygen fugacity on basalt magma fractionation trends. Methodological principles of the use of COMAGMAT were discussed based on its thermodynamical and empirical basis, including specific details of the model calibration. Using COMAGMAT-3.5 a set of phase equilibria calculations (called Geochemical Thermometry) has been conducted for six cumulative rocks from the Marginal Border Series of the Skaergaard intrusion. As a result, initial magma temperature (1165±10°C) and trapped melt composition proposed to be parental magma to the Skaergaard intrusion were determined. Computer simulations of perfect fractionation of this composition as well as another proposed parent produced petrochemical trends opposite to those followed from natural observations. This is interpreted as evidence for an initial Skaergaard magma containing a large amount of olivine and plagioclase crystals (about 40–45%), so that the proposed and calculated parents are related through the melt trapped in the crystal–liquid mixture. This promotes the conclusion that the Skaergaard magma fractionation process was intermediate between equilibrium and fractional crystallization. In this case the classic Wager's trend should be considered an exception rather than a rule for the differentiation of ferro-basaltic magmas. A polybaric version of COMAGMAT has been applied for the genetic interpretation of a volcanic suite from the Klyuchevskoi volcano, Kamchatka, Russia. To identify petrological processes responsible for the observed suite ranging from high-magnesia to high-alumina basalts, we used the model to simulate the Klyuchevskoi suite assuming isobaric crystallization of a parental HMB magma at a variety of pressures and a separate set of simulations assuming fractionation during continuous magma ascent from a depth of 60 km. These results indicate that the Klyuchevskoi trend can be produced by 40% fractionation of Ol–Aug–Sp±Opx assemblages during ascent of the parental HMB magma over the pressure range 19–7 kbar with the rate of decompression being 0.33 kbar/% crystallized (at 1350–1110°C), with 2 wt.% of H2O in the initial melt and 3 wt.% of H2O in the resultant high-Al basalt.  相似文献   

3.
A surprisingly simple and precise major element mass balance is consistent with derivation of average upper mantle peridotite from a partially molten chondritic Earth by subtraction of perovskite and addition of olivine. Majorite involvement is precluded unless some as yet unidentified components play a role. Perovskite subtraction during a primordial melting event is expected to occur by crystal fractionation at depth, while olivine addition is accomplished by a combination of buoyancy mechanisms: crystal flotation from a deep layer of melt buried by its own compressibility to the base of the solidifying upper mantle and subsequent solid state convection of this buoyant magnesian olivine upward. These processes are consistent with known density relations of crystals and liquid at very high pressure. Mass balance predicts that the residual magma body at depth after supplying olivine by flotation upward can be komatiitic. Distribution of originally C1 chrondritic bulk Earth material a few 100 m.y. after primordial differentiation is solid peridotite upper mantle, perovskite lower mantle, and a komatiitic liquid sandwich horizon.  相似文献   

4.
The existence of Archaean komatiites with eruption temperatures greater than 1650°C requires that the mantle be vertically differentiated by the time of komatiite eruption. If in the unlikely event that undifferentiated mantle had survived primordial planetary differentiation and had been hot enough to deliver 1650°C komatiite, it would have been extensively molten to depths of ～250 km, resulting in rapid, profound, vertical differentiation anyway. During primordial differentiation (or Archaean komatiite petrogenesis) the high density and compressibility of ultrabasic melt allowed storage of a global melt layer beneath a buoyant residue of dunite and/or harzburgite. This refractory cap segregated by extraction of melt both upwards and downwards from the depth at which the density contrast between crystals and liquid vanishes. Eruption of komatiite from the melt layer by corrosion of the cap was the Archaean earth's principal means of dissipating excess heat. This subterranean magma ocean precluded vertical homogenization of the Archaean mantle by convection but effectively absorbed lateral mantle heterogeneities and imposed the relative uniformity of maximum eruption temperature and MgO contents (～32%) seen in primitive Archaean komatiites on all continents.Verification of the postulated density relations of liquids and crystals to 100 kbar becomes a pressing concern in view of the expected consequences these relations may have had.  相似文献   

5.
Spinifex-textured sills (i.e., veins) characterized by komatiitic magmas that have intruded their own volcanic-piles have long been recognized. For instance, in the early 1970s, Pyke and coworkers, in their classic work at Pyke Hill in Munro Township, noted that not all spinifex-bearing ultramafic rocks formed as lava flows, rather some were clearly emplaced as small dikes and sills. Several hypotheses have been proposed to explain spinifex-textured sills: intrusion into a cold host, filter pressing, or drainage of residual liquid. However, these do not satisfactorily explain the phenomenon. Field and petrographic observations at Pyke Hill and Serpentine Mountain demonstrate that spinifex-bearing komatiite sills and dikes were emplaced during channel inflation processes when new magma was intruded into a cooler, semi-consolidated but permeable cumulate material. Komatiitic liquids were intruded into the olivine cumulate rocks near the boundary between the spinifex and the cumulate zones of well-organized to organized komatiite flows. Spinifex-textured sills are generally tabular in morphology, stacked one above another, with curviplanar contacts sub-parallel to stratigraphy. Some sills exhibit complex digitated apophyses. Thinner sills typically have a random olivine spinifex texture similar, though generally composed of coarser crystals, to that of komatiite lava flows. Thicker sills exhibit more complex organization of their constituent crystals characterized by zones of random olivine spinifex, overlying zones of organized coarse spinifex crystals similar to those found in lava flows. They have striking coarse dendritic spinifex zones composed of very large olivine crystals, up to several centimetres long and up to 1 cm wide that are not observed in lava flows. Typically, at the sill margins, the cumulate material of the host flow is composed of euhedral to subhedral olivine crystals that are larger than those distal to the contact. Many of these margin-crystals have either concentric overgrowth shells or dendritic olivine overgrowths that grew from the cumulate-sill contact toward the sill interior. The dendrites grew on pre-existing olivine cumulate at the contact in response to a sharp temperature gradient imposed by the intrusion of hot material, whereas the concentric overgrowths formed as new melt percolated into the unconsolidated groundmass of the host-flow cumulate material. Spinifex-textured sills and dikes occur in well-organized to organized flows that are interpreted to have formed by “breakouts” above and peripheral to lava pathways (channels/conduits) as a result of inflation that accompanied voluminous komatiitic eruptions responsible for the construction and channelization of komatiitic flow fields. The spinifex-textured dikes and sills represent komatiitic lava that was originally emplaced into the channel roof during periods of episodic inflation that resulted in lava breakouts and was subsequently trapped in the “roof rocks” during periods of channel deflation. Accordingly, the occurrence of spinifex-textured sills and dikes may indicate proximity to, and aid in the identification and delineation of lava channel-ways that could potentially host Ni–Cu–(PGE) mineralization within komatiitic lava flow-fields.  相似文献   

6.
Rare earth element abundances have been measured in pyroxenitic (19.6% MgO) to gabbroic (7.7% MgO) rocks from the upper part of a thick, layered komatiite lava flow (Fred's Flow) in Munro Township, Ontario. This flow apparently erupted as a highly basic liquid which subsequently differentiated into layers of ultramafic cumulate rocks and a basaltic residual liquid. The analyzed rocks have compositions and spinifex or equigranular textures interpreted to indicate that they represent the complete range of liquids that were present during the differentiation of the lava.All the analyzed rocks are depleted in light REE, and also exhibit a slight depletion of Yb and Er relative to Gd and Dy. Chondrite-normalized Ce and Yb abundances range from 3.2 to 7.8 and 5.1 to 9.7 respectively. Proportions of fractionating minerals were estimated using a major element petrological mixing program and petrographic data. REE modeling based on these results indicates that the dominant process relating the samples is low-pressure fractional crystallization of olivine, followed at lower temperatures by clinopyroxene and plagioclase. Except for Eu, correspondence between observed and calculated REE abundances obviates any need to appeal to processes of major REE redistribution during diagenesis and low-grade metamorphism. Major differences in REE patterns of other ultramafic and mafic komatiitic lava flows [6,11], therefore, probably reflect different episodes of partial melting and/or differences in mantle source composition. The consistency of the REE in the layered flow, however, supports the concept that mafic komatiites can also be derived from ultrabasic parental magmas by low-pressure fractional crystallization. The light-REE-depleted patterns of these komatiites resemble those of modern MORB, suggesting that the mantle source of the komatiites had undergone a previous melting episode.  相似文献   

7.
Late Cenozoic alkali basalts in the Ganseong area of South Korea contain abundant ultramafic xenoliths and clinopyroxene megacrysts. Anhydrous clinopyroxene‐rich wehrlite–clinopyroxenites make up the majority of the xenolith population and range from wehrlite through olivine clinopyroxenite to clinopyroxenite. This study investigates the petrogenesis of wehrlite–clinopyroxenite xenoliths and clinopyroxene megacrysts on the basis of petrography and mineral and whole‐rock chemistry. Observations such as an absence of carbonate or apatite, high Ti/Eu ratio, and clinopyroxene‐dominated mineralogy lead us to rule out peridotite–melt reactions as the origin of the Ganseong wehrlites– olivine clinopyroxenites. The whole‐rock compositions (e.g. high abundance of CaO at a given MgO content and low abundance of incompatible elements, such as U, K, P, and Ti compared with mafic melts) indicate that the pyroxenites do not represent crystallized magma itself, but are rather cumulates with a small amount of residual liquid. Anhydrous and orthopyroxene‐free mineral assemblages, crystallization sequence of olivine→clinopyroxene→plagioclase, and mineral chemistries (e.g. low Cr# and high TiO2 abundances in spinels and high TiO2 and Na2O abundances in clinopyroxenes at a given Mg#) suggest that relatively anhydrous intraplate alkaline basalt is the most likely candidate for the parent magma. Texture and compositions of the clinopyroxene megacrysts preclude a cognate origin via high‐pressure crystallization of the host magma. The clinopyroxene megacrysts occupy the Fe‐rich end of the compositional trends defined by wehrlite–pyroxenite clinopyroxenes. Progressive decreases in Mg# and an absence of significant compositional gaps between pyroxenite xenoliths and clinopyroxene megacrysts indicate fractionation and differentiation of a similar parental magma. We suggest that the clinopyroxene megacrysts represent fragments of pegmatitic clinopyroxenites crystallized from more advanced fractionation stages of the evolution of a series of magmatic liquids formed Ganseong wehrlite–clinopyroxenites.  相似文献   

8.
Layered ultramafic-gabbro bodies occur widely in the Archaean of northwest Scotland. They were metamorphosed at granulite or high amphibolite facies and were tectonically thinned and broken up during deformation. They comprise repeated ultramafic-gabbro layers, locally with Ni-poor sulphide-rich tops, each rhythmic unit showing decreasing MgO, Ni and normative anorthite with stratigraphic height. Major, trace and rare earth element data are presented for the range of rock types. In ultramafic rocks, MgO varies from 22 to 37 wt.%, Ni from 1000 to 2500 ppm and TiO2 from 0.08 to 0.40 wt.%, while the MgO content of the gabbros ranges from 14 to 6 wt.%. The REE patterns are flat to LREE enriched with no significant Eu anomalies. In ultramafic rocks REE are from 4 to 10 times chondrite, and in the gabbros LREE range from 8 to 30 times chondrite and HREE from 6 to 15 times chondrite. Study of incompatible elements (Ti, Zr, Y) which are relatively immobile during metamorphism shows that neither garnet nor hornblende were involved in fractionation. Trace element modelling shows it is improbable that the ultramafic rocks represent primary MgO-rich liquids even though their incompatible element contents are quite high. The chemical trends are interpreted in terms of olivine and pyroxene settling from a tholeiitic high-Mg magma with 15–20 wt.% MgO derived by 30–40% partial melting of an undepleted mantle. The ultramafic rocks are the cumulates and the gabbros the derived liquids.  相似文献   

9.
The south flank of Kilauea Volcano is unstable and has the structure of a huge landslide; it is one of at least 17 enormous catastrophic landslides shed from the Hawaiian Islands. Mechanisms previously proposed for movement of the south flank invoke slip of the volcanic pile over seafloor sediments. Slip on a low friction décollement alone cannot explain why the thickest and widest sector of the flank moves more rapidly than the rest, or why this section contains a 300 km3 aseismic volume above the seismically defined décollement. It is proposed that this aseismic volume, adjacent to the caldera in the direction of flank slip, consists of olivine cumulates that creep outward, pushing the south flank seawards. Average primary Kilauea tholeiitic magma contains about 16.5 wt.% MgO compared with an average 10 wt.% MgO for erupted subaerial and submarine basalts. This difference requires fractionation of 17 wt.% (14 vol.%) olivine phenocrysts that accumulate near the base of the magma reservoir where they form cumulates. Submarine-erupted Kilauea lavas contain abundant deformed olivine xenocrysts derived from these cumulates. Deformed dunite formed during the tholeiitic shield stage is also erupted as xenoliths in subsequent alkalic lavas. The deformation structures in olivine xenocrysts suggest that the cumulus olivine was densely packed, probably with as little as 5–10 vol.% intercumulus liquid, before entrainment of the xenocrysts. The olivine cumulates were at magmatic temperatures (>1100°C) when the xenocrysts were entrained. Olivine at 1100°C has a rheology similar to ice, and the olivine cumulates should flow down and away from the summit of the volcano. Flow of the olivine cumulates places constant pressure on the unbuttressed seaward flank, leading to an extensional region that localizes deep intrusions behind the flank; these intrusions add to the seaward push. This mechanism ties the source of gravitational instability to the caldera complex and deep rift systems and, therefore, limits catastrophic sector failure of Hawaiian volcanoes to their active growth phase, when the core of olivine cumulates is still hot enough to flow.  相似文献   

10.
Volcanological and petrological data suggest that the Phlegraean Fields volcanic activity has been fed, at least in the last 10,500 years, by a not-refilled magma chamber where trachytic residual liquids were produced by fractionation of a trachybasaltic magma. Using estimated volumes of the erupted products andP–T data obtained through petrological studies, a conductive thermal model of the chamber was built up in order to estimate its past and present size. Results suggest a volume decrease from approximately 14 to 1.4 km3 of the trachybasaltic magma in 10,500 years. Trachytic liquid would also be present in the chamber in a minimum amount of 0.4 km3. The model allowed some insights on the petrogenesis of the Phlegraean trachytes, suggesting that they were erupted as liquids because thermally buffered within the magma chamber.  相似文献   

11.
This paper provides new constraints on the crystallization conditions of the 3.49 Ga Barberton komatiites. The compositional evidence from igneous pyroxene in the olivine spinifex komatiite units indicates that the magma contained significant quantities of dissolved H2O. Estimates are made from comparisons of the compositions of pyroxene preserved in Barberton komatiites with pyroxene produced in laboratory experiments at 0.1 MPa (1 bar) under anhydrous conditions and at 100 and 200 MPa (1 and 2 kbar) under H2O-saturated conditions on an analog Barberton composition. Pyroxene thermobarometry on high-Ca clinopyroxene compositions from ten samples requires a range of minimum magmatic water contents of 6 wt.% or greater at the time of pyroxene crystallization and minimum emplacement pressures of 190 MPa (6 km depth). Since high-Ca pyroxene appears after 30% crystallization of olivine and spinel, the liquidus H2O contents could be 4 to 6 wt.% H2O. The liquidus temperature of the Barberton komatiite composition studied is between 1370 and 1400°C at 200 MPa under H2O-saturated conditions. When compared to the temperature-depth regime of modern melt generation environments, the komatiite mantle source temperatures are 200°C higher than the hydrous mantle melting temperatures inferred in modern subduction zone environments and 100°C higher than mean mantle melting temperatures estimated at mid-ocean ridges. When compared to previous estimates of komatiite liquidus temperatures, melting under hydrous conditions occurs at temperatures that are 250°C lower than previous estimates for anhydrous komatiite. Mantle melting by near-fractional, adiabatic decompression takes place in a melting column that spans 38 km depth range under hydrous conditions. This depth interval for melting is only slightly greater than that observed in modern mid-ocean ridge environments. In contrast, anhydrous fractional melting models of komatiite occur over a larger depth range ( 130 km) and place the base of the melting column into the transition zone.  相似文献   

12.
Tholeiitic basalt glasses from the FAMOUS area of the Mid-Atlantic Ridge are among the most primitive basaltic liquids reported from the ocean basins. One of the more primitive of these[Mg/(Mg+Fe2+) = 0.68;Ni= 232ppm;TiO2 = 0.61] glasses (572-1-1) was selected for an experimental investigation. This study found olivine to be the liquidus phase from 1 atm to 10.5 kbar where it is replaced by clinopyroxene. The sequence of appearance of phases at 1 atm pressure is olivine (1268°C), plagioclase (1235°C) and clinopyroxene (1135°C). The sample is multiply saturated at 10.5 kbar with olivine (Fo88), clinopyroxene (Wo32En60Fs9), and orthopyroxene (Wo5En83Fs12). From the 1-atm data we have measured (FeO/MgO) olivine/(FeO*/MgO) liquid (K′D) for olivine-melt pairs equilibrated at 12 temperatures in the range 1268–1205°C.K′D varies from 0.30 at 1205°C to 0.27 at 1268°C. Analysis of high-pressure olivine melt pairs indicates a systematic increase inK′D with pressure.Evaluation of the 1-atm experiments reveals that fractionation of olivine followed by olivine + plagioclase can generate much of the variation in major element chemistry observed in the FAMOUS basalt glasses. However, it cannot account for the entire spectrum of glass compositions — particularly with respect to TiO2 and Na2O. The variations in these components are such as to require different primary liquids.Comparison of clinopyroxene microphenocrysts/xenocrysts found in oceanic tholeiites with experimental clinopyroxenes reveal that the majority of those in the tholeiites may have crystallized from the magma at pressures greater than ～ 10 kbar and are not accidental xenocrysts. Clinopyroxene fractionation at high pressures may be a viable mechanism for fractionating basaltic magmas.The major and minor element mineral/meltK′d's from our experiments have been used to model the source region residual mineralogy for given percentages of partial melting. These data suggest that ～20% partial melting of a lherzolite source containing 0–10% clinopyroxene can generate the major and minor element concentrations in the parental magmas of the Project FAMOUS basalt glasses.  相似文献   

13.
The volcanic history of Somma-Vesuvius indicates that salic products compatible with an origin by fractionation within a shallow magma chamber have been repeatedly erupted («Plinian» pumice deposits). The last two of these eruptions, (79 A.D. and 3500 B.P.) were carefully studied. Interaction with calcareous country rocks had limited importance, and all data indicate that differentiated magmas were produced by crystal-liquid fractionation within the undersaturated part of petrogeny’s residua system at about 1 kb water pressure. The solid-liquid trend indicates that the derivative magmas originated by fractionation of slightly but significantly different parental liquids. Some lavas of appropriate composition were selected as parental liquids to compute the entity of the fractionation. Results suggest that in both bases a fractionation of about 70 weight % was needed to produce liquids with the composition of the pumice. The combination of all data indicates that the two Plinian eruptions were fed by a magma chamber (3–4 km deep) having a volume of approx. 2.0–2.5 km3. The temperature of the magma that initially entered the chamber was about 1100°C, whereas the temperature of the residual liquids erupted was Plinian pumice was 800° and 850°C respectively. There is no evidence that such a magma chamber existed at Vesuvius after the 79 A.D. eruption. These results have relevant practical implications for volcanic hazard and monitoring and for geothermal energy.  相似文献   

14.
Major, minor and trace element abundances were determined in seven Angra dos Reis samples including whole rocks, fassaite (clinopyroxene), olivine and whitlockite separates via sequential instrumental neutron activation analysis. The chondritic normalized rare earth element (REE) abundance pattern for the Angra dos Reis clinopyroxene separates shows a concave downward shape with a small negative Eu anomaly. The strong fractionation between the light and the heavy REE in olivine separates could be attributed to the presence of islands of kirschsteinite in the olivines. The large-ion lithophile trace elements were highly enriched in the whitlockite separate as expected (e.g. La ≈ 370 ppm). The lower Hf and Sc abundances in whitlockite compared to that in the equilibrium “magma” could be the result of favorable partitioning of Hf and Sc in baddeleyite, which may have crystallized prior to or with whitlockite in the interstitial liquid. Comparison of whole rock with mineral separate data shows the presence of ～3% olivine, ～2.6% spinel and small amounts of metallic Ni-Fe and troilite in the whole rock.The trace element abundances in the derivative magma from which the Angra dos Reis clinopyroxene crystallized were estimated from the clinopyroxene data and the clinopyroxene mineral-liquid partition coefficients. From the derivative magma, the trace element abundances in the possible parent magmas were calculated by assuming that these parent magmas have undergone different degrees of clinopyroxene fractional crystallization to yield the Angra dos Reis derivative magma. Using the trace element abundances in these possible parent magmas, a two-stage crystal-liquid fractionation model with source material containing olivine, orthopyroxene and clinopyroxene is presented for the genesis of Angra dos Reis. Possible combinations of the degree of equilibrium non-modal partial melting, the source mineral composition and the initial element abundances required to generate possible Angra dos Reis parent magmas are calculated by the multilinear regression analysis method. Favorable solutions for this two-stage crystal-liquid fractionation model could be that Angra dos Reis crystallized at ～70% fractional crystallization of clinopyroxene from magmas generated by reasonable degrees of equilibrium partial melting (～7–10%) of deep-seated primitive source materials (olivine ～54–30%, orthopyroxene ～33–53%, and clinopyroxene ～13–17%) with trace element (Ba, Sr, REE and Sc) abundances ～3.5–4.7 × chondrites. These calculated REE abundances in the Angra dos Reis parent body are very similar to those suggested for the primordial moon (～3–5 × chondrites).Possible genetic relationships between Angra dos Reis and other achondrites, especially cumulate eucrites and nakhlites, are studied. Apparently, the unique Angra dos Reis could not be related to those achondrites by crystal-liquid fractionation of the same parent body.  相似文献   

15.
High pressure experiments using the sink/float method have bracketed the density of hydrous iron-rich ultrabasic silicate melt from 1.35 to 10.0 GPa at temperatures from 1400 to 1860 °C. The silicate melt composition was a 50–50 mixture of natural komatiite and synthetic fayalite. Water was added in the form of brucite Mg(OH)2 and was present in the experimental run products at 2 wt.% and 5 wt.% levels as confirmed by microprobe analyses of total oxygen. Buoyancy marker spheres were olivines and garnets of known composition and density. The density of the silicate melt with 5 wt.% water at 2 GPa and 1500 °C is 0.192 g cm? 3 less than the anhydrous form of this melt at the same P and T. This density difference gives a partial molar volume of water in silicate melt of ～ 7 cm3 mol? 1, which is similar to previous studies at high pressure. The komatiite–fayalite liquids with 0 and 2 wt.% H2O, have extrapolated density crossovers with equilibrium liquidus olivine at 8 and 9 GPa respectively, but there is no crossover for the liquid with 5 wt.% H2O. These results are consistent with the hypothesis that dense hydrous melts could be gravitationally stable atop the 410 km discontinuity in the Earth. The results also support the notion that equilibrium liquidus olivine could float in an FeO-rich hydrous martian magma ocean. Extrapolation of the data suggests that FeO-rich hydrous melt could be negatively buoyant in the Earth's D″-region or atop the core–mantle-boundary (CMB), although experiments at higher pressure are needed to confirm this prediction.  相似文献   

16.
Nickel partitioning between olivine and silicate melt   总被引：1，自引：0，他引：1  
Partitioning of Ni between olivine and silicate melt has been determined for compositions in the system Fo-Ab-An (1 atm) for temperatures ranging from 1250°C to 1450°C. Nickel concentrations were determined by electron microprobe; concentration levels in the liquids ranged from 0.1% to 0.5%. Platinum capsules or Pt wire loops were used as containers. Equilibrium was evaluated from kinetic considerations and by variation of run parameters; it was documented in one case by a bracketed reversal. No evidence was found for a dependence of the partition coefficient D (Ni in olivine/Ni in liquid) on Ni concentration. D is strongly dependent on melt composition, varying linearly with (1/MgO) at constant temperature. The intrinsic temperature dependence of D is small; the apparent temperature dependence reported in previous studies is largely related to the variation of melt composition with temperature. Our D values determined in the simple system Fo-An-Ab agree well with those reported by Leeman for natural (Fe-bearing) basalt systems. Overall variation of D in our system (and in natural basalts) can be expressed by the regression: D = (124/MgO) ? 0.9Our data are used to evaluate published Ni-MgO relationships in natural basalt series from Kilauea, Crozet, Cape Verde and Baffin Bay. A combination of olivine accumulation and fractional crystallization processes are sufficient to model these series. Using our data, unique “parental” liquids can be specified for each of these series; the MgO content of these liquids varies from 6% to 13%. Basalts with MgO contents greater than these “parental” liquids must be accumulative. The linear Ni-MgO trends, high absolute Ni concentrations, and large spread of Ni contents for the high-MgO basalts argue convincingly against their being “primary” liquids. Models such as those of O'Hara [6,13] and Clarke [24], based on the assertion of primary high-MgO liquids, must therefore be re-evaluated.Because of the high Si/O ratio and low MgO content of island arc andesites, the Ni partition coefficient D may be quite high. Therefore, the relatively low Ni content of such andesites may not be an argument against their derivation as direct partial melts of the mantle.  相似文献   

17.
Silicate melt inclusions in phenocrysts are not directly representative of trapped magmatic liquid because chemical interaction between inclusions and host crystals usually occurs after melt entrapment. However, if more than one phenocryst type in a suite of rocks contains melt inclusions, the original trapped-liquid composition can be accurately fixed by the intersection of host-mineral fractionation lines in a triangular oxide plot of inclusion analyses. When plotted on a CaO—MgO—Al2O3 triangular diagram, analyses of inclusions in plagioclase, olivine, and clinopyroxene from a basalt dredged off Bouvet Island fall along crystal fractionation lines that intersect at a single point. This point represents an initial trapped liquid composition rich in CaO and MgO, and low in TiO2 and total alkalies. The composition is transitional between tholeiite and basaltic komatiite, and may be indicative of extensive melting of clinopyroxene in the mantle.  相似文献   

18.
The lunar crust at the Apollo 16 landing site contains substantial amounts of a “primitive component” in which the ferromagnesian group of elements is concentrated. The composition of this component can be retrieved via an analysis of mixing relationships displayed by lunar breccias. It is found to be a komatiite which is compositionally similar to terrestrial komatiites both in major and minor elements. The komatiite component of the lunar crust is believed to have formed by extensive degrees of melting of the lunar interior at depths greater than were involved in the formation of the lunar magma ocean which was parental to the crust. After formation of the anorthositic crust, it was invaded by extensive flows and intrusions of komatiite magma from these deeper source regions. The komatiites became intimately mixed with the anorthosite by intensive meteoroid impacts about 4.5 b.y. ago, thereby accounting for the observed mixing relationships displayed by the crust. The compositional similarity between lunar and terrestrial komatiites strongly implies a corresponding similarity between the compositions of their source regions in the lunar interior and the Earth's upper mantle. The composition of the lunar interior can be modelled more specifically by combining the komatiite composition with its liquidus olivine composition (as determined experimentally) in proportions chosen so as to produce a cosmochemically acceptable range of Mg/Si ratios for the bulk Moon. Except for higher FeO and lower Na2O, the range of compositions thereby obtained for the bulk moon is very similar to the composition of the Earth's upper mantle.The effects of meteoritic contamination on the abundances of cobalt and nickel in lunar highland breccias were subtracted on the assumption that the contaminating projectiles were chondritic. The cobalt and nickel residuals thereby obtained were found to correlate strongly with the (Mg + Fe) content of the breccias, demonstrating that the Co and Ni are associated with the ferromagnesian component of the breccias and are genuinely indigenous to the Moon. The lunar highland Co and Ni residuals also display striking Ni/Co versus Ni correlations which follow a similar trend to those displayed by terrestrial basalts, picrites and komatiites. The lunar trends provide further decisive evidence of the indigenous nature of the Co and Ni residuals and suggest the operation of extensive fractionation controlled by olivine-liquid equilibria in producing the primitive component of the lunar breccias. Indigenous nickel abundances at the Apollo 14, 15 and 17 sites are much lower than at the Apollo 16 site, although rocks from all sites follow the same Ni/Co versus Ni trends. It is suggested that the primitive component at the Apollo 14, 15 and 17 sites was generally of basaltic composition, in contrast to the komatiitic nature of the Apollo 16 primitive component.  相似文献   

19.
The lavas of the 1955 east rift eruption of Kilauea Volcano have been the object of considerable petrologic interest for two reasons. First, the early 1955 lavas are among the most differentiated ever erupted at Kilauea, and second, the petrographic character and chemical composition of the lava being erupted changed significantly during the eruption. This shift, from more differentiated (MgO=5.0–5.7%) to more magnesian (MgO=6.2–6.8%) lava, has been variously interpreted, as either due to systematic excavation of a zoned, differentiated magma body, or to invasion of the differentiated magma by more primitive magma, followed by rapid mixing and eruption of the resulting hybrid magmas. Petrologic examination of several nearvent spatter samples of the late 1955 lavas shows abundant evidence for magma mixing, including resorbed and/or reversely zoned crystals of olivine, augite and plagioclase. In addition, the compositional ranges of olivine, plagioclase and groundmass sulfide are very large, implying that the assemblages are hybrid. Core compositions of olivine phenocrysts range from Fo85 to Fo77. The most magnesian olivines in these samples must have originally crystallized from a melt containing 8.0–8.5% MgO, which is distinctly more magnesian than the bulk composition of the late 1955 lavas. The majorelement and trace-element data are either permissive or supportive of a hybrid origin for the late 1955 lavas. In particular, the compositional trends of the 1955 lavas on plots of CaO vs MgO, and the virtual invariance of Al2O3 and Sr in these plagioclase-phyric lavas are more easily explained by magma mixing than by fractionation. The pattern of internal disequilibrium/re-equilibration in the late 1955 spatter samples is consistent with reintrusion and mixing having occurred at least twice, during the latter part of the 1955 eruption. Plagioclase zonation preserves possible evidence for additional, earlier reintrusion events. Least-squares modelling the mixing of early 1955 bulk compositions with various summit lavas±olivine pick the 1952 summit lava as most like the primitive component. The results also indicate the primitive component had MgO=7.5–8.0%, corresponding to liquidus temperatures of 1165–1175°C. The absence of Fe-Ti oxide phenocrysts in the late 1955 lavas implies that the cooler component of the hybrid had T>1110°C. Thus the thermal contrast between the two components may have been as much as 55–65°C, sufficient to produce the conspicuous disequilibrium effects visible in the spatter samples.  相似文献   

20.
 The Puu Oo eruption has been remarkable in the historical record of Kilauea Volcano for its duration (over 13 years), volume (>1 km3) and compositional variation (5.7–10 wt.% MgO). During the summer of 1986, the main vent for lava production moved 3 km down the east rift zone and the eruption style changed from episodic geyser-like fountaining at Puu Oo to virtually continuous, relatively quiescent effusion at the Kupaianaha vent. This paper examines this next chapter in the Puu Oo eruption, episodes 48 and 49, and presents new ICP-MS trace element and Pb-, Sr-, and Nd-isotope data for the entire eruption (1983–1994). Nearly aphyric to weakly olivine-phyric lavas were erupted during episodes 48 and 49. The variation in MgO content of Kupaianaha lavas erupted before 1990 correlates with changes in tilt at the summit of Kilauea, both of which probably were controlled by variations in Kilauea's magma supply rate. These lavas contain euhedral olivines which generally are in equilibrium with whole-rock compositions, although some of the more mafic lavas which erupted during 1990, a period of frequent pauses in the eruption, accumulated 2–4 vol.% olivine. The highest forsterite content of olivines (∼85%) in Kupaianaha lavas indicates that the parental magmas for these lavas had MgO contents of ∼10 wt.%, which equals the highest observed value for lavas during this eruption. The composition of the Puu Oo lavas has progressively changed during the eruption. Since early 1985 (episode 30), when mixing between an evolved rift zone magma and a more mafic summit reservoir-derived magma ended, the normalized (to 10 wt.% MgO) abundances of highly incompatible elements and CaO have systematically decreased with time, whereas ratios of these trace elements and Pb, Sr, and Nd isotopes, and the abundances of Y and Yb, have remained relatively unchanged. These results indicate that the Hawaiian plume source for Puu Oo magmas must be relatively homogeneous on a scale of 10–20 km3 (assuming 5–10% partial melting), and that localized melting within the plume has apparently progressively depleted its incompatible elements and clinopyroxene component as the eruption continued. The rate of variation of highly incompatible elements in Puu Oo lavas is much greater than that observed for Kilauea historical summit lavas (e.g., Ba/Y 0.09 a–1 vs ∼0.03 a–1). This rapid change indicates that Puu Oo magmas did not mix thoroughly with magma in the summit reservoir. Thus, except for variable amounts of olivine fractionation, the geochemical variation in these lavas is predominantly controlled by mantle processes. Received: 8 March 1996 / Accepted: 30 April 1996  相似文献   

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