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1.
Samples from the surface of lava flows discharged by the 2012–2013 Tolbachik Fissure Eruption were found to contain oxysulfates of copper, sodium, and potassium: K2Cu3O(SO4)2 (fedotovite), NaKCu2O(SO4)2, and Na3K5Cu8O4(SO4)8. The last two phases have no naturally occurring or synthetic analogues that we are aware of. They form flattened crystals of prismatic to long-prismatic habits. The crystals of Na3K5Cu8O4(SO4)8 have a chemical composition corresponding to the empirical formula Na2.22K5.47Cu8.02S8.05O36. An X-ray analysis of this compound showed that it has a monoclinic symmetry, P2/c, a = 13.909(4), b = 4.977(1), c = 23.525(6) Å, β = 90.021(5)°, V = 1628.3(7) Å3. The crystal structure was determined by direct techniques and refined to yield R 1 for 3955 reflexes//web// with F 2 > 4σF. The compound NaKCu2O(SO4)2 also belongs to the monoclinic system, P2/c, a = 14.111(4), b = 4.946(1), c = 23.673(6) Å, β = 92.052(6)°, V = 1651.1(8) Å3. The structure was determined by direct techniques to yield a tentative structural model that has been refined up to R 1 = 0.135 for 4088 reflexes with F 2 > 4σF. The crystal structure of Na3K5Cu8O4(SO4)8 is based on chains of [O2Cu4]4+ consisting of rib-coupled oxy-centered tetrahedrons of (OCu4)6+. The chains are surrounded by sulfate radicals, resulting in columns of {[O2Cu4](SO4)4}4? aligned along the b axis. The interchain space contains completely ordered positions of Na+ and K+ cations. The principle underlying the connection of NaKCu2O(SO4)2 columns in the crystal structure of {[O2Cu4](SO4)4}4? is different, in view of the relation Na:K = 1 as contrasted with 3:5 for the compound Na3K5Cu8O4(SO4)8. The presence of oxy-centered tetrahedrons in the structure of these new compounds furnishes an indirect hint at the importance of polynuclear copper-oxygen radicals with centering oxygen atoms as forms of transport of copper by volcanic gases.  相似文献   

2.
Inclusions of ferropericlase and former (Mg,Fe)(Si,Al)O3 perovskite in diamonds from Kankan, Guinea believed to originate in the lower mantle were studied using Mössbauer spectroscopy to determine Fe3+/ΣFe. Fe3+ concentration in the (Mg,Fe)(Si,Al)O3 inclusion is consistent with empirical relations relating Fe3+/ΣFe to Al concentration, supporting the inference that it crystallised in the perovskite structure at lower mantle conditions. In ferropericlase there is a nearly linear variation of trivalent cation abundance with monovalent cation abundance, suggesting a substitution of the form Na0.5M0.53+O (M=Fe3+, Cr3+, Al3+). Excess positive charge is likely balanced by cation vacancies, where their abundance is observed to increase with increasing iron concentration, consistent with high-pressure experiments. The abundance of cation vacancies is related to oxygen fugacity, where ferropericlase inclusions from Kankan and São Luiz (Brazil) are inferred to have formed at conditions more oxidising than Fe-(Mg,Fe)O equilibrium, but more reducing than Re-ReO2 equilibrium. Fe2+/Mg partition coefficients between (Mg,Fe)(Si,Al)O3 and ferropericlase were calculated for inclusions co-existing in the same diamond using Mössbauer data and empirical relations based on high-pressure experimental work. Most values are consistent with high-pressure experiments, suggesting that these inclusions equilibrated at lower mantle conditions. The measured ferropericlase Fe3+ concentrations are consistent with diamond formation in a region of redox gradients, possibly arising from the subduction of oxidised material into reduced lower mantle. Reduction of carbonate to form ferropericlase and diamond is consistent with a slight shift of Kankan δ13C values to isotopically heavy compositions compared to the worldwide dataset, and could supply the oxygen necessary to satisfy the high Fe3+ concentration in (Mg,Fe)(Si,Al)O3 perovskite, as well as account for the high proportion of ferropericlase in the lower mantle paragenesis. The heterogeneity of lower mantle diamond sources indicates that the composition of lower mantle diamonds do not necessarily reflect those of the bulk mantle.  相似文献   

3.
A new phase which is much denser than the component oxides of spinel (MgAl2O4) was synthesised at loading pressures greater than 250 kbar and at about 1000°C in a diamond-anvil press coupled with laser heating. The new phase (ε-MgAl2O4) was indexed on the basis of an orthorhombic cell with a = 8.507 ± 0.004, b = 2.740 ± 0.003, c = 9.407 ± 0.005Å, and Z = 4 at room temperature and 1 bar pressure. Thus the molar volume for ε-MgAl2O4 at the above conditions was calculated to be 33.01 ± 0.07 cm3, which is 10.3% less than that of the mixture corundum plus periclase. The dense phase of spinel found in shock-wave experiments can be reasonably interpreted as ε-MgAl2O4, and this may be a potentially important mineral component of the earth's lower mantle. The new structure may also provide a possible candidate for the dense phases of Fe3O4 and Mg2SiO4 which were found by shock experiments.  相似文献   

4.
Magnetic properties and crystal structure parameters of synthetic solid solutions Fe3O4Fe3TiO4, Fe2O4MgFe2O4 and Fe3O4Mg2TiO4 have been studied. Basic regularities in the behaviour of saturation magnetisation (Is), Curie temperature (TC) and cubic lattice parameter a during the substitution of Ti and Mg ions for Fe ions have been found. As the concentration of Ti ions increases, Is reduces from 70 Gs·cm3 g?1 to 0, TC changes from 580 to 130°C and a from 8.391 to 8.520 Å. Growth of the Mg concentration leads to changes in Is to 19.8 Gs·cm3, g?1, TC, to 440°C and a, to 8.360 Å. The full Fe ions substitution gives “a”=8.440 A?.Chemical compositions of the samples, in which the valency variation of Fe ions at oxidation leads to an increase in susceptibility and TC, have been determined.  相似文献   

5.
Single-crystal spectra of pyropes, synthesized on the 3:1:3 composition of the system MgO-Al2O3-SiO2 atpH2O = ptotal = 25kbar and 1000°C, show a broad band centered at around 3400 cm?1 due toνH2O of (H2O)n aggregates in fluid inclusions and a sharp intense band near 3600 cm?1 due toνOH of (HO)44? clusters introduced by the hydrogarnet substitutionSi4+ = 4H+. The water contents in the synthetic pyrope, due to (HO)44? clusters are estimated near 0.05 wt.% H2O from spectroscopic data. Si deficits in microprobe analyses of the pyropes studied support the hydrogarnet substitution. These results show that the hydrogarnet substitution in pyrope may contribute to water contents in the mantle.  相似文献   

6.
The oxidation state of iron can significantly influence the physical and chemical properties of lower mantle minerals. To improve methods for estimation of Fe3+/∑Fe, synthetic assemblages of (Mg,Fe)(Si,Al)O3 perovskite and (Mg,Fe)O ferropericlase were synthesised from oxide starting mixtures in Re or Fe capsules at 26 GPa and 1650-1850 °C using a multianvil press. (Mg,Fe)(Si,Al)O3 majorite was also present in some of the run products. Both electron energy loss spectra (EELS) and Mössbauer spectra were measured for each run product, and a robust fitting method was developed for Mössbauer spectra using EELS results as a standard that enabled Fe3+/∑Fe of (Mg,Fe)(Si,Al)O3 perovskite to be determined from Mössbauer spectra of multiphase assemblages. There is a close to linear variation between Fe3+/∑Fe and Al concentration in (Mg,Fe)(Si,Al)O3 perovskite, independent of oxygen fugacity. The concentration of Fe3+ in (Mg,Fe)O increases with increasing iron concentration along curves of constant oxygen fugacity, where higher oxygen fugacity stabilises greater Fe3+ concentrations. Fe2+/Mg partition coefficients calculated from chemical composition data corrected for measured Fe3+/∑Fe showed values nearly identical within experimental error for all samples, and independent of Al concentration and oxygen fugacity. Simple empirical relations were derived to calculate Fe3+/∑Fe in (Mg,Fe)(Si,Al)O3 perovskite and (Mg,Fe)O ferropericlase samples for which no Mössbauer or EELS data were available, and tested by applying them to calculation of Fe2+/Mg partition coefficients from literature data for (Mg,Fe)(Si,Al)O3 perovskite-(Mg,Fe)O assemblages where only total iron concentrations had been measured. Results showed Fe2+/Mg partition coefficients that were equal to existing values within experimental error, hence confirming the validity of the empirical relations.  相似文献   

7.
The orthorhombic MgSiO3 perovskite has been synthesized with the aid of a double-stage split-sphere-type high-pressure apparatus at about 280 kbar and 1000°C. The unit cell dimensions are: a = 4.7754(3)Å, b = 4.9292(4)Å and c = 6.8969(5)Å with the probable space group Pbnm. Calculated density is 4.108 g cm?3. Crystal structure determination has been carried out by means of both the geometrical simulation (DLS) technique and the ordinary powder X-ray analysis. The results indicate that the MgSiO3 perovskite is closer to the ideal perovskite than ScAlO3 perovskite.  相似文献   

8.
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   

9.
Hydrothermal experiments in the temperature range 750–1020°C have defined the saturation behavior of zircon in crustal anatectic melts as a function of both temperature and composition. The results provide a model of zircon solubility given by: In DZrzircon/melt= ?3.80?[0.85(M?1)]+12900/T where DZrzircon/melt is the concentration ratio of Zr in the stoichiometric zircon to that in the melt, T is the absolute temperature, and M is the cation ratio (Na + K + 2Ca)/(Al · Si). This solubility model is based principally upon experiments at 860°, 930°, and 1020°C, but has also been confirmed at temperatures up to 1500°C for M = 1.3. The lowest temperature experiments (750° and 800°C) yielded relatively imprecise, low solubilities, but the measured values (with assigned errors) are nevertheless in agreement with the predictions of the model.For M = 1.3 (a normal peraluminous granite), these results predict zircon solubilities ranging from ～ 100 ppm dissolved Zr at 750°C to 1330 ppm at 1020°C. Thus, in view of the substantial range of bulk Zr concentrations observed in crustal granitoids (～ 50–350 ppm), it is clear that anatectic magmas can show contrasting behavior toward zircon in the source rock. Those melts containing insufficient Zr for saturation in zircon during melting can have achieved that condition only by consuming all zircon in the source. On the other hand, melts with higher Zr contents (appropriate to saturation in zircon) must be regarded as incapable of dissolving additional zircon, whether it be located in the residual rocks or as crystals entrained in the departing melt fraction. This latter possibility is particularly interesting, inasmuch as the inability of a melt to consume zircon means that critical geochemical “indicators” contained in the undissolved zircon (e.g. heavy rare earths, Hf, U, Th, and radiogenic Pb) can equilibrate with the contacting melt only by solid-state diffusion, which may be slow relative to the time scale of the melting event.  相似文献   

10.
Structure refinement of astrophyllite   总被引：1，自引：0，他引：1  
The crystal structure of astrophyllite K2Na(Fe, Mn, Mg,□)7[Ti2(Si4O12)2|O3](OH, F)4 has been refined. The dimensions of the triclinic unit cell are: a = 0.5359(2) nm,b = 1.1614(4) nm, c = 1.1861(4) nm, α= 113.16(2)°, β= 103.04(2)°,γ= 94.56(2)°,V = 0.6495(5) nm3, Z= 1, space group P1, R=0.057 for 5308 reflections |Fo|>3σ|Fo|. According to structural and compositional differences the monoclinic astrophyllite K2NaNa(Fe, Mn)4Mg2Ti2[Si4O12]2(OH)4(OH, F)2 and astrophyllite should be considered as two different mineral species. Astrophyllite, monoclinic astrophyllite, bafertisite and lamprophyllite contain heteropolyhedral sheets which topologically are related with Si, O sheets of mica where one or several SiO4 tetrahedra are replaced by TiO n polyhedra. Therefore this heterophyllotitanosilicate series represents a kind of functional substitution in inorganic crystals.  相似文献   

11.
Studies of the sulphur hydrolysis reaction, 4S + 4H2O /ag 3H2S + HSO4? + H+, were conducted between 200 and 320°C in sealed silica glass tubes. The isotope exchange reaction: H218O + HS16O4? /ag H216O + HS18O4? is so rapid at the low pH (1.5–3) as to be unquenchable. However, the sulphur isotope exchange reaction: H234S+ H32SO4? /ag H232S + H34SO4? gave t12 values of 0.1, 0.3 and 1.7 days at 320, 260 and 200°C respectively and equilibrium H2S - HSO4? sulphur isotope fractionation values of 20.9, 22.4, 24.8, 26.7 and 29.3‰ at 320, 290, 260, 230 and 200°C respectively. This latter data is represented by: 1000lnα(HSO4??H2S) = 5.07 (106T?2) + 6.33, and has valuable applications in geothermal and ore deposit studies.  相似文献   

12.
The effect of patchy colonies of the invasive zebra mussel (Dreissena polymorpha) on sedimentary processes was investigated in a mesotrophic lake (Plateliai Lake, Lithuania). Benthic fluxes of O2, TCO2, CH4, Mn2+, Fe2+, N2, the inorganic forms of N, Si and P and dissolved organic C and N were quantified by dark incubations of sediments cores, with and without D. polymorpha. Individual mussels also were incubated for metabolic measurements. Sediments with D. polymorpha had significantly higher O2 and TCO2 fluxes and displayed higher rates of denitrification. The presence of mussels also resulted in higher regeneration of P and N (mostly as ammonium) while the effect on Si was not significant. However, likely due to the low zebra mussel biomass (57.2 ± 25.3 gSFDW m?2), biodeposition has not changed the ratio between anaerobic and total respiration. Methane and reduced metals fluxes were in fact similar in the presence and absence of D. polymorpha. Incubations of mussels without sediments confirmed that bivalve metabolism was the main driver of benthic respiration and nutrient recycling. Nitrate production suggested the presence of nitrifiers associated with the molluscs. The main outcome of this study was that zebra mussels alter the quantity and the stoichiometry of nutrients regenerated by the benthic compartment. The enhancement of nitrogen loss via denitrification, by a factor of 1.5, was much less pronounced than the increase in ammonium recycling rate, stimulated by a factor of 33. Negligible PO4 3? fluxes in bare sediments (?3.4 ± 6.8 μmol m?2 h?1) increased in the presence of mussels and considerable amounts of this nutrient (69.6 ± 29.4 μmol m?2 h?1) were mobilized to the water column. Further research should address other nutrient sources to the lake to verify whether altered rates and stoichiometry of benthic regeneration can affect primary producer community composition and activity.  相似文献   

13.
A single crystal of untwinned orthopyroxene from lunar anorthosite sample 15415, with composition (Mg1.14Fe0.80Mn0.02Ca0.04)(Si1.97Al0.03)O6, has a unit cell in space groupPbca witha = 18.310(15)Å,b = 8.904(10)Å,c = 5.214(7)Å, containing 2 formula units. A set of 742 counter-measured intensity data made with MoKα radiation has been used to refine the crystal structure in isotropic thermal mode toR = 0.116. Anisotropic refinement led toR = 0.092, but thermal parameters are distorted by non-random errors resulting from poor crystal texture. The resulting structure is in close agreement with that obtained by Ghose [9] for a hypersthene from Greenland. A parameterq, which gives (MgqFe1?q) for cation siteM(1) and (Mg1.14?qFeq?0.18Ca0.04) for siteM(2), was included in the least-squares analysis, yieldingq = 0.90(1).This orthopyroxene has the high degree of cation order expected of pyroxenes subjected to Apollonian metamorphism at lower than 500–600°C. No evidence exists for a subsequent thermal event of sufficient intensity to disorder the pyroxene. On the basis of previous laboratory studies of argon-release patterns of lunar plagioclase and order-disorder kinetics of terrestrial pyroxenes, we attribute the reported isotopic age (3.9–4.1 AE) to cessation of metamorphism, perhaps caused by impact excavation.  相似文献   

14.
FAMOUS basalt 527-1-1 (a high-Mg oceanic pillow basalt) has three generations of spinel which can be distinguished petrographically and chemically. The first generation (Group I) have reaction coronas and are high in Al2O3. The second generation (Group II) have no reaction coronas and are high in Cr2O3 and the third generation (Group III) are small, late-stage spinels with intermediate Al2O3 and Cr2O3. Experimental synthesis of spinels from fused rock powder of this basalt was carried out at temperatures of 1175–1270°C and oxygen fugacities of 10?5.5 to 10?10 atm at 1 atm pressure. Spinel is the liquidus phase at oxygen fugacities of 10?8.5 atm and higher but it does not crystallize at any temperature at oxygen fugacities less than 10?9.5. The composition of our spinels synthesized at 1230–1250°C and 10?9 atmfO2 are most similar to the high-Cr spinels (Group II) found in the rock. Spinels synthesized at 1200°C and 10?8.5 atmO2 are chemically similar to the Group III spinels in 527-1-1. We did not synthesize spinel at any temperature or oxygen fugacity that are similar to the high-Al (Group I) spinel found in 527-1-1. These results indicate that the high-Cr (Group II) spinel is the liquidus phase in 527-1-1 at low pressure and Group III spinel crystallize below the liquidus (～1200°C) after eruption of the basalt on the sea floor. The high-Al spinel (Group I) could have crystallized at high pressure or from a magma enriched in Al and perhaps Mg compared to 527-1-1.  相似文献   

15.
The sorption of Eu species onto nano-size silica-water interfaces is investigated at pH range of 1―8.5 and the initial Eu concentrations (CEu) of 2×10−5, 2×10−4 and 2×10−3 M using fluorescence spectroscopy. The sorption rate of Eu is initially low, but significantly increases at pH > 4. For the initial CEu of 2×10−5, 2×10−4 and 2×10−3 M, the dissolved Eu species are completely sorbed onto silica-water interfaces at pH = 4.75, −5.8 and 6.6, respectively, with the respective sorption densities of −1.58×10−8, 1.58×10−7 and 1.58×10−6 mol/m2. The sorbed Eu species at pH < 6 is aquo Eu3+, which is sorbed onto silica-water interfaces as an outer-sphere complex at pH < 5, but may be sorbed as an inner-sphere bidentate complex at 5 < pH < 6, due to the decrease of the NH2O to −6 at pH = 6. At pH = 6 – 8, Eu(OH)2+, Eu(CO3)+and Eu(CO3)2 − form in the solutions, and Eu(CO3)+is dominant at pH = −7.5. These ions may be sorbed onto silica-water interfaces as inner-sphere bidentate complexes or multi-nuclear pre-cipitates.  相似文献   

16.
The Queershan composite granitic pluton is located in the north of the late Paleozoic Yidun arc collision-orogenic belt, eastern Tibetan Plateau. The main rock types are coarse-grained porphyritic alkalic-monzonite granite with minor fine-grained porphyritic monzogranite and granodiorite distributed in the eastern and southwestern regions. Here we report their zircon U-Pb ages and geo- chemical data. The intrusive contact relations indicate that granodiorite was formed earlier than the alkalic-monzonite granite(105.9±1.3 Ma) and monzogranite(102.6±1.1 Ma). These suggest that the Queershan composite granitic pluton was formed through three-stage magmatic events. The alkalic-monzonite granite(105.9±1.3 Ma) and monzogranite(102.6±1.1 Ma) are characterized by high SiO2(73.5%–77.7%), K2O+Na2O(6.9%–8.5%), Ga/Al ratios(2.6–3.4) and low Al2O3(11.8%–14.5%), CaO(0.25%–1.5%), MgO(0.18%–0.69%), negative Ba, Sr and Eu anomalies, showing A-type granite affinities. The granodiorite exhibits lower SiO2, P2O5 and K2O+Na2O contents, but higher Al2O3, CaO and MgO contents than alkalic-monzonite granite and monzogranite, showing I-type granite affinity. 176Hf/177 Hf ratios of the alkalic-monzonite granite and the monzogranite are 0.282692–0.282749 and 0.282685–0.282765, respectively, and with similar ?Hf(t) values(?0.56 to 1.43 and ?0.87 to 1.90 respectively). They also present similar TDM2 model ages(1.04–1.22 and 1.07–1.2 Ga respectively), indicating they may be sourced from a similar rock source, mostly like Kangding Complex. The homogeneity of the Hf isotopic compositions and the absence of the MMEs demonstrate that little depleted mantle materials have contributed to the source. We propose that the Mesoproterozoic crust materials of the Yangtze Craton exist beneath the Yidun arc terrane and support it was a dismembered part of the Yangtze Craton. The A-type granites of Queershan composite granitic pluton are most probably related to the closure of the Bangong-Nujiang Tethys ocean.  相似文献   

17.
We present the main seismological results of our study of the Campania-Lucania earthquake of 23 November 1980. A complete set of far field and local data has been analysed. From long-period body waves data we determine the fault plane solution (φ1 = 140°,δ1 = 60°,φ2 = 75°,δ2 = 54°), a depth of 15 km and calculate a seismic moment of 6 × 1025 dyne cm and a source duration of 6 s. From data of a local network deployed immediately after the event we determine aftershock locations: they are aligned in a direction NW-SE that fit extremely well with the focal solution determined above. We can choose as fault plane the plane striking 140° and dipping at 60° and the event is a normal event with a large component of left-lateral strike slip. The source area evaluated from this aftershock distribution 14 km × 40 km is quite suitable for an earthquake of a seismic moment of 6 × 1025 dyne cm.  相似文献   

18.
The high pressure spinel polymorph of Ni2SiO4 persists metastably at 713°C and atmospheric pressure. The enthalpy of the olivine-spinel transition was obtained by measuring the heats of solution of both polymorphs in a molten oxide solvent, 2PbO · B2O3, at that temperature. For Ni2SiO4(ol)→Ni2SiO4, ΔH9860 = +1.4 ± 0.7kcal/mol. The heat content increments, H986 ? H297, were found to be: olivine, 25.73 ± 0.42kcal/mol, and spinel, 25.39 ± 0.20kcal/mol. The measured enthalpy of the transformation is consistent with the low slope of the phase boundary, ?P/?T = ～ 12b/deg, observed by Akimoto and others. The entropy of the olivine-spinel transition in Ni2SiO4 is accordingly about a factor of three smaller in magnitude (ΔS = ～ ?1cal/deg mol) than that for Co2SiO4,Fe2SiO4,Mg2SiO4or Mg2GeO4 (ΔS = ?3to?3.5cal/deg mol).  相似文献   

19.
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   

20.
Four pyroxenes with compositions En48Fs48Wo4, En47·5Fs47·5Wo5, En45Fs45Wo10 and En40Fs40Wo20, synthesized at 1200°C at atmospheric pressure, were heat-treated at 500, 600, 700, and 800°C for various lengths of time. These pyroxenes are variously ordered with respect to Fe2+ and Mg2+ without unmixing. The Fe2+-Mg2+ distribution over the two nonequivalent sites M1 and M2, determined through Mössbauer spectroscopy, is found to be a function of both temperature and concentration of Ca2+ at the M2 site. The preference of Fe2+ for the M2 site increases with decreasing temperature and increasing Ca2+. These data can be used to determine cation equilibration temperatures of lunar and terrestrial pigeonites. The lunar pigeonites usually indicate equilibration temperatures of 700–860°C, except the pigeonite from rock 14053, which may have been subjected to shock heating due to meteoritic impact.  相似文献   

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