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1.
Three groups of spinels have been identified in dredged basalts from the Mid-Atlantic Ridge in the Azores region (30–40°N): (1) magnesiochromites with 0.4–0.5 Cr/(Cr + Al) are most common and characteristic of olivine tholeiites of the region; (2) titaniferous magnesiochromites are found in an olivine basalt with alkali affinities, of local occurrence and evolved in relatively high fugacity of oxygen; (3) chromian spinels with 0.23 Cr/(Cr + Al) occur in unusual high-Al picrites of local occurrence and possible high-pressure origin. Spinels are restricted in occurrence to the least fractionated lavas, with FeO*/FeO* + MgO ratio less than 0.575 and with Cr content greater than 350 ppm. A close relationship between Al content of liquidus spinel and Al content of magma has been observed for basaltic types. High-Al spinels deviating from this relationship, such as those found in picritic lavas from the Mid-Atlantic Ridge, may have crystallized at high pressure. The use of spinels as geobarometers in magmas of a restricted compositional range seems a promising prospect. There is no evidence of systematic variation in spinel chemistry of occurrence along the Mid-Atlantic Ridge, such as could be related to different mantle sources of the basalts, plume versus non-plume or binary mantle mixing.  相似文献   

2.
The electrical conductivity of a single crystal of San Carlos olivine (Fo92, 0.16 wt.% Fe2O3) has been measured as a function of temperature and oxygen fugacity (fO2). After heating to 1338°C at fO2 = 10?12 atm., the conductivity at 950°C was 10?5 (ohm-m)?1, almost 3 orders of magnitude less than that measured in air. This decrease is due to the reduction of Fe3+ to Fe2+. Further heating to 1500°C at fO2 = 10?14 atm., decreased the electrical conductivity at 950°C to 10?6 (ohm-m)?1. When recovered at room temperature, the speciment had Fo96 composition and contained small, opaque blebs distributed throughout the crystal. Derivations of temperature profiles for the earth's mantle from conductivity-depth models must take account of the important role played by iron oxidation state in the electrical conductivity of olivine.  相似文献   

3.
The textures of chondrules have been reproduced by crystallizing melts of three different compositions at 1 atm with cooling rates ranging from 400 to 20°C/min under 10?9 to 10?12 atmPO2. A porphyritic olivine texture has been formed from a melt of olivine-rich composition (SiO2 = 45 wt.%), a barred-olivine texture from melt of intermediate composition (SiO2 = 47 wt.%), and radial-olivine texture from melt of pyroxene-rich composition (SiO2 = 57 wt.%). The cooling rate for producing barred olivine is most restricted; the rate ranges from 120 to 50°C/min. Other textures can be formed with wider ranges of cooling rate. The results of the experiments indicate that some of the major types of textures of chondrules can be formed with cooling rate of about 100°C/min. With this cooling rate, the texture varies depending on the composition of melt.  相似文献   

4.
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   

5.
Chemical studies of two ophiolite suites and of selected mid-oceanic rift (MOR) regions indicate the presence of certain magmatic compositions: basalt, Fe-enriched basalt, and sodium granite (plagiogranite). There is a notable lack of evidence for melts of intermediate composition (i.e. 50–60 wt.% SiO2). To determine possible relationships between basic rocks (basalts and gabbros) and acidic rocks (plagiogranites) a primitive basalt was fractionated at low pressure, under anhydrous conditions, and at different oxygen fugacities near the iron-wustite buffer and slightly above the quartz-fayalite-magnetite buffer. Samples of this basalt were taken to slightly above liquidus temperatures and then cooled at rates ranging from 1 to 2°C/hr. A liquid line of descent characterized by an Fe enrichment was delineated by quenching these experiments from a final temperature in the range of 1200 to 1000°C and analyzing the residual liquid (glass). After 95% crystallization of olivine, plagioclase, calcium pyroxene, and ilmenite, the residual liquid was an Fe-enriched basalt. This Fe-enriched basalt became immiscible at a temperature of about 1010°C. The immiscible phases produced were a more Fe-enriched basaltic liquid and a granitic liquid. The granitic liquid is similar in composition to the naturally occurring plagiogranites found in small volumes in ophiolites and in certain MOR regions. It is therefore concluded that silicate liquid immiscibility could be the petrogenetic process responsible for producing plagiogranite in some MOR regions and in some ophiolites. On the other hand, plagiogranites in ophiolites and MOR rock suites having andesitic and dacitic composition rocks may have evolved under conditions more closely approximating equilibrium crystallization and/or they may have evolved at high water pressures. The available experimental data suggest that amphibole would crystallize early and yield SiO2-enriched liquids at depths greater than 4.5 km for PH2O's in the range 0.6–1.0 Ptotal.The major problem in interpreting any of the natural plagiogranites as products of silicate liquid immiscibility is the fact that neither the Fe-enriched conjugate liquid or its crystalline equivalent has been described in the ophiolite or MOR literature. The identification of this Fe-rich conjugate magma is essential in any rock suite if a completely convincing case for silicate liquid immiscibility is to be made.  相似文献   

6.
At moderate temperatures, the elastic properties of natural MgAl2O4 spinel differ in several significant ways from properties of synthetic spinels. Below 1000 K, the ultrasonic resonant frequencies of an ordered natural spinel change significantly after heat treatment; at higher temperatures, both types of spinels have similar resonant responses. The temperature derivatives of the elastic constants of an ordered spinel also differ from those of disordered spinels at moderate temperatures; again, at higher temperatures, both types of spinels have similar behaviors. The Raman spectra also differ below 1000 K for ordered natural and disordered spinels and are similar at higher temperatures and after cooling to ambient temperature. We associate these changes in ultrasonic resonance and Raman spectra of spinel with cation disordering at high temperature which may be quenched by cooling. We deduce estimates of the inversion parameter from the relative intensities of the two A1g Raman modes in very good agreement with estimates made from other measurements. We find thatC 11 andC 12 decrease by 4 and 8%, respectively, with 20% inversion in spinel;C 44 is less sensitive to cation order. These results imply that previous measurements of the adiabatic elastic constants of spinels at ambient conditions have been affected by the state of cation disorder of the specimen.  相似文献   

7.
Plagioclases in the 1974 high-Al basalt from Fuego Volcano have δO18 values of +6.0 to +8.5 per mil. Meteoric water cannot have played a significant role in Fuego’s magma. Large, weakly zone clear phenocrysts had δO18 values in the accepted mantle range, while patchyzoned and oscillatory-zoned plagioclases inferred to have formed later and shallower levels have slightly heavier oxygen isotopic ratios.  相似文献   

8.
The matrix of 77135 would not be a liquid at less than 1280°C, 1 atm pressure. The petrography and lack of evidence of crystallization in the 1280-1150°C interval suggest that the matrix is either a devitrified, shock-melted and supercooled glass, or a devitrified, depressurised liquid whose liquidus temperature had been depressed by the presence of a small amount of water at pressures attainable in the upper part of the lunar crust. Devitrification fronts would have advanced faster than 1 mm min?1 in 77135 glass at 1050°C under lunar surface conditions.  相似文献   

9.
Experimental study of the phase boundary for the disproportionation of the inverse spinel Mg2SnO4 into its isochemical mixed oxides indicates a slope dP/dT = 40 ± 10bars/°K. This positive slope is consistent with the large entropies of inverse (relative to normal) spinels predicted from high-temperature entropy-molar volume systematics. Thermodynamic data do not support the existence of a distinctly negative slope for the proposed disproportionation of Mg2SiO4 normal spinel. Evidence from X-ray and phase equilibria studies suggests the possibility that Si4+, Mg2+, and Fe2+ share the octahedral sites in silicate spinels under mantle conditions. The consequences of this partial inverse character are a positive slope for the postulated spinel-mixed oxide phase boundary near 650 km depth, removal of a widely accepted constraint on mantle-wide convection, and anomalous elasticity-density behaviour within the transition zone.  相似文献   

10.
Reaction coronas of pyroxene ± ilmenite occur around clasts of olivine in Apollo 14 high-grade metamorphic breccias. In experiments of several months duration, there was no evidence of corona formation at 1000°C, but at 1050°, withfO2 at or above Ilm-Ru-Fe and below Fe-Fe1?x O, incipient coronas formed around Fo50–70 in synthetic 14311 matrix. In addition, withfO2 controlled by Ilm-Ru-Fe at 1050°C, the olivines reduced to Fo68, En69 + Fe. Reduction of olivine under these conditions is inconsistent with the calculated stability relations and is attributed to uncertainties in the activity coefficient for olivine or pyroxene. The experiments also suggest that vesicularity in the Apollo 14 high-grade breccias may correlate with the amount of glassy material in their unmetamorphosed precursors. The metamorphic event is attributed to burial in a hot ejecta blanket, such as that of the Imbrium event.  相似文献   

11.
High-temperature experiments on ferromagnesian compositions have been hampered by the rapid absorption of up to 95% of the original iron by platinum and 40% by silver-palladium capsules. Molybdenum or iron capsule materials can decrease or alleviate iron loss, but restrict oxygen fugacities to values near the iron-wustite buffer. Because Co2+ is stable at fO2 =HM and because the solubility of Co in platinum in this range of fO2 is ～0.05% at temperatures to 1350°C, its use as an analogue for Fe2+ is possible. In addition, experiments simulating various Fe2+ ratios can be easily performed by choosing appropriate Co2+/Fe3+ ratios. The cobalt phases produced possess brilliant and distinctive colors which are valuable aids in optical identification of minute phases. The cobalt analogue hypothesis was tested with atmospheric pressure experiments in air on the cobalt analogue of the 1921 Kilauea basalt at three simulated Fe2+/Fe3+ ratios. The results were compared with those of R.E.T. Hill (1969) for the natural 1921 basalt. The phase relations were the same, with the cobalt system stability fields systematically shifted by about +50°C. Microprobe analysis of olivines and the coexisting glasses indicate that the distribution of Co2+ between olivine and melt is independent of temperature and liquid composition. Although the analogue liquid composition differs from the equilibrium composition of the natural system, it may be corrected be employing distribution coefficients (KD = 0.61 for the Co system; KD = 0.33 for the Fe system) to closely approximate what the natural system would yield if iron loss did not occur.  相似文献   

12.
Melting relations of a glassy magnesian olivine tholeiite from the FAMOUS area have been studied within the pressure range 1 atm to 15 kbar. From 1 atm to 10 kbar, olivine is the liquidus phase, followed by plagioclase and Ca-rich clinopyroxene. Above 10 kbar, Ca-rich clinopyroxene appears on the liquidus, followed by orthopyroxene and spinel. Near 10 kbar, olivine, orthopyroxene, clinopyroxene, spinel and plagioclase crystallize within 10°C of the liquidus. This indicates that a liquid of this magnesian olivine tholeiite composition could coexist with mantle peridotite at about 10 kbar. This result is in agreement with the geochemistry of Ni; the Ni concentration of the studied sample corresponds to the theoretical concentration in a primary magma [14,15].These data suggest that at least some magnesian mid-oceanic ridge basalts (MORBs) could be primary melts segregated from the mantle at depths near the transition zone between plagioclase lherzolite and spinel lherzolite (about 10 kbar). Based on this model, the residual mantle after extraction of MORBs should be lherzolite, not harzburgite.High-pressure (7–10 kbar) fractionation models involving olivine, plagioclase and clinopyroxene, which have been proposed by several workers (e.g. [36]) to explain the varieties of MORBs, were re-emphasized based on this melting study. The rare occurrence of clinopyroxene as a phenocryst phase in MORBs is explained by precipitation in a magma chamber at high pressure, or by dissolution of clinopyroxene formed earlier at high pressure.  相似文献   

13.
Ultrasonic compressional wave velocity Vp and quality factor Qp have been measured in alkali basalt, olivine basalt and basic andesite melts in the frequency range of 3.4–22 MHz and in the temperature range of 1100–1400°C. Velocity and attenuation of the melts depend on frequency and temperature, showing that there are relaxation mechanisms in the melts. Complex moduli are calculated from the ultrasonic data. The results fit well a complex modulus of Arrhenius temperature dependence with log-normal Gaussian distribution in relaxation times of attenuation. The analysis yields average relaxation time, its activation energy, relaxed modulus, unrelaxed modulus and width of Gaussian distribution in relaxation times. Relaxed modulus is smaller (17.5 GPa) for basic andesite melt of high silica and high alumina contents than for the other two basalt melts (18.1–18.4 GPa). The most probable relaxation times decrease from ～ 3 × 10?10 s for basic andesite to ～ 10?11 s for alkali basalt at 1400°C. Activation energies of attenuation, ranging from 270 to 340 kJ mol?1 in the three melts, are highest in basic andesite. Longitudinal viscosity values and their temperature dependences are also calculated from Vp and Qp data. The volume viscosity values are estimated from the data using the shear viscosity values. Longitudinal, volume and shear viscosities and their activation energies are highest in the basic andesite melt of the most polymerized structure.  相似文献   

14.
Inclusions consisting of clinopyroxene, amphibole, Fe-Ti oxides and apatitc are abundant in the Roque Nublo volcanics, a unit of Late Tertiary age that is widespread on Gran Canaria Island. The unit includes alkalic basalts and breccias. Mafic minerals in several inclusions and in one basalt host have been analysed with the electron microprobe. Although the inclusions vary in size, texture and mineralogy, they show certain common teatures. The pyroxenes analyzed are all salites-augites and their position in the Ca-Fe Mg quadrilateral suggests that they are early formed representatives of the pyroxene crystallization trend characteristic of alkaliolivine basalt. The amphibole is invariably kaersutite. A common variety of inclusion is composed largely of kaersutite and titaniferous clinopyroxene. The kaersutite (TiO2 5.27%, K2O 1.58%) is homogeneous, except for slight iron enrichment in the margins of crystals. The clinopyroxene is an hourglass-zoned, brownish titansalite, Ca 50 Mg 35 Fe 15, TiO2 3.08%, with a green core of Ca 49 Mg 38 Fe 13, TiO2 2.15%. Compositions of coexisting titanilerous magnetite and ilmenite, Usp 44 Mt 56 and Ilm 85 Hem 15, respectively, indicate they formed at approximately 975°C and pO, 10?10.5 atm. In another type of inclusion and its host basalt, pyroxene relations are more complex. Inclusion pyroxene is markedly but diffusely zoned. Predominant is a green salite, Ca 47 Mg 38 Fe 15, TiO2 1.11%, which has small, patchy core zones of brownish. Ti-rich salite. Ca 48 Mg 35 Fe 17, TiO2 1.94%. Cores of crystals in the host basalt are Ca 47 Mg 41 Fe 12, TiO2 2.23%; rims are pale green, Cr-rich diopsidic augite, Ca 44 Mg 45 Fe 11, TiO2 1.32%, Cr2O3 0.48%. This «reverse» Fe-Mg zoning is attributed to increasing partial pressure of oxygen as crystallization proceeded. Kaersutite similar to that mentioned above occurs in both the inclusion and its host, in which it is highly resorbed. The available field and analytical evidence strongly suggests that the inclusions and the associated basalts are genetically related. Resorption of the kaersutite at depth may have given rise to the alkalic basalts of the Roque Nublo series.  相似文献   

15.
Magnesium orthosilicate with spinel structure (γ-Mg2SiO4) was synthesized at about 250 kbar and 1000°C. Unit cell dimension was established to be 8.076 ± 0.001Å. X-ray powder diffraction pattern revealed a significant difference between γ-Mg2SiO4 and other γ-M2SiO4 spinels (M = Fe, Co, and Ni) in the intensities of (111) and (331) reflections, both of which are virtually absent in the Mg2SiO4 spinel. This feature could be thoroughly understood by the calculation of the intensities for several silicate spinels.  相似文献   

16.
The trajectory of the North Atlantic Deep Water is traced from 65°N to 20°N latitude. Along this track the dissolved O2 decreases, theδ18O of the dissolved O2 increases, and the14C content of the water decreases. From these observations the rate of in-situ O2 utilization in the deep water is calculated to be 0.10 μmol kg?1 yr?1. As was observed previously in the Pacific, theδ18O data presented here indicate that the utilization is probably caused by bacterial respiration. Carbon dioxide is being added to the water at the rate of 0.07 μmol kg?1 yr?1 from the oxidation of this organic matter. An additional 0.12 μmol kg?1 yr?1 of CO2 is derived from the dissolution of particles of CaCO3.  相似文献   

17.
Interstitial waters were extracted from cores at three locations in the eastern equatorial Pacific and analyzed for nutrients, dissolved carbonate species, Mn and Fe. From the depth variation in pore water chemistry, we infer that organic matter oxidation reactions occur with depth in the following sequence: O2 reduction, NO3? and MnO2 reduction, and then ferric iron reduction. From NO3? results we infer that O2 is largely or totally consumed within the top few centimeters of sediment. NO3? is completely reduced at a sediment depth of 20 cm at a site near the crest of the East Pacific Rise, but is preserved at levels of 20–30 μmol/kg at 40 cm depth at a Guatemala Basin site.We have calculated the alkalinity for pore water samples assuming ions diffuse according to relative ionic diffusion coefficients, that the stoichiometry of organic matter oxidation reactions is that of “Redfield” organic matter, and that the pore waters are saturated throughout with respect to CaCO3. The measured alkalinity increase is only about half of the predicted value. The difference is probably a result of either enhanced mixing of the pore water in the top few centimeters of sediments by biological or physical processes, or the occurrence of an inorganic reaction which consumes alkalinity.At depths of oxygen and nitrate reduction in the sediments, the ion concentration product of CaCO3 is the same, within the analytical error, as the solubility product of Ingle et al. [34] at 1 atm and 4°C. This result indicates CaCO3 resaturation on pressure change during coring. Where pore water Mn concentrations become measurable, the ion concentration product increases, indicating either supersaturation with respect to calcite or that another phase is controlling the carbonate solubility.  相似文献   

18.
Along the east coast of the Andaman Islands, abundant detrital chromian spinels frequently occur in black sands at the confluence of streams meeting the Andaman Sea. The mineral chemistry of these detrital chromian spinels has been used in reconstructing the evolutionary history of the Andaman ophiolite. The chromian spinels show wide variation in compositional parameters such as Cr# [= Cr/(Cr + A1) atomic ratio] (0.13–0.91), Mg# [= Mg/(Mg + Fe2+) atomic ratio] (0.23–0.76), and TiO2 (<0.05–3.9 wt%). The YFe3+[= 100Fe3+/(Cr + A1 + Fe3+) atomic ratio] is remarkably low (usually <10 except for south Andaman). The ranges of chemical composition of chromian spinels are different in each locality. The spinel compositions show very depleted signatures over the entire island, which suggests that all massifs in the Andaman ophiolite were affected under island‐arc conditions. Although the degree of depletion varies in different parts of the island, a directional change in composition of the detrital chromian spinels from south to north is evident. Towards the north the detrital chromian spinels point to less‐depleted source rocks in contrast to relatively more depleted towards the south. The possibilities to explain this directional change are critically discussed in the context of the evolution of Andaman ophiolite.  相似文献   

19.
The Sindong Group was deposited in the north–south trending half‐graben Nakdong Trough, southern Korean peninsula. The occurrence of detrital chromian spinels from the Jinju Formation of the Sindong Group in the Gyeongsang Basin means that the mafic to ultramafic rocks were exposed in its provenance. The chromian spinels from the Jinju Formation are characterized by extremely low TiO2 and Fe3+. Moreover, their range of Cr# is from 0.45 to 0.80 and makes a single trend with Mg#. The chemistry of chromian spinels implies that the source rocks for chromian spinels were peridotites or serpentinites, which originated in the mantle wedge. To more narrowly constrain their source rocks, the Ulsan and Andong serpentinites exposed in the Gyeongsang Basin were examined petrographically. Chromian spinels in the Andong serpentinite differ from those of the Jinju Formation and those in the Ulsan serpentinite partly resemble them. Furthermore, the Jinju chromian spinel suite is similar to the detrital chromian spinels from the Mesozoic sediments in the Circum‐Hida Tectonic zone, which includes the Nagato Tectonic zone in Southwest Japan and the Joetsu Belt in Northeast Japan. This suggests that the basement rocks, which were located along the main fault bounding the eastern edge of the Nakdong Trough, had exposures of peridotite or serpentinite. It is possible that the Nakdong Trough was directly adjacent to the Circum‐Hida Tectonic zone before the opening of the Sea of Japan (East Sea).  相似文献   

20.
Summary The photolysis of ozone in the u.v. Hartley Band produces metastable oxygen atoms and molecules. At wavelengths shorter than 3100 Å the primary quantum yield is probably unity but greater uncertainty exists about its value at longer wavelengths. At 2500 Å, O2(1g) is produced with near unit efficiency and there is some evidence that singlet O2 is also a primary prduct at the short wavelenght end of the Huggins band. O2(1 g + ) is not a primary photolytic product at 2500 Å but is produced as a secondary product from the rapid reaction of O(1D) with ground state O2. O(1D) reacts rapidly with O3 although the nature of the products of this reaction has not been unequivocally established and there is now strong evidence against the occurrence of energy chains in dry ozone. The reaction of O(3P) atoms with O3 has been found to have an activation energy of 4.4 kcal mole–1.  相似文献   

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