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1.
When melts of Ca–Al inclusions in chondrites, which are dominated by the oxides SiO2, MgO, CaO, and Al2O3, evaporate at high temperatures, the SiO2 and MgO fugacities are inverted: SiO2, which is more volatile than MgO, becomes less volatile when melts rich in refractory CaO and Al2O3 evaporate. This fugacity inversion can be realistically explained within the framework of D.S. Korzhinskii’s theory of acid–base interaction between components in silicate melts. According to this theory, an increase in CaO concentration in the melt increases its basicity, and this, in turn, increases the activity (and hence, also fugacity) of MgO and decreases those of SiO2. In the real compositions of the Ca–Al inclusions in chondrites, the MgO/SiO2 ratio systematically decreases with an increase in the CaO concentration under the effect of acid–base interaction.  相似文献   

2.
Melt and fluid inclusions have been studied in olivine phenocrysts (Fo 81–79) from trachybasalts of the Southern Baikal volcanic area, Dzhida field. The melt inclusions were homogenized, quenched, and analyzed on an electron and ion microprobe. The study of homogenized glasses of nine inclusions showed that basaltic melts (SiO2 = 47.1–50.3 wt %, MgO = 5.0–7.7 wt %, CaO = 7.1–11.1 wt %) have high contents of Al2O3 (17.1–19.6 wt %), Na2O (4.1–6.2 wt %), K2O (2.2–3.3 wt %), and P2O5 (0.6–1.1 wt %). The volatile contents are low (in wt %): 0.24–0.31 H2O, 0.08 F, 0.03 Cl, and 0.02 S. Primary fluid inclusions in olivines from four trachybasalt samples contain high-density CO2 (0.73–0.87 g/cm3), indicating a CO2 fluid pressure of 4.3–6.6 kbar at 1200–1300°C and olivine crystallization depths of 16–24 km. Ion microprobe analyses of 20 glasses from melt inclusions for trace elements showed that the magmas of the Baikal rift were enriched in incompatible elements, thus differing from oceanic rift basalts and resembling oceanic island basalts. A comparison of our data on melt and fluid inclusions in olivine from trachybasalts of the Dzhida field with preexisting data on the Eastern Tuva volcanic highland in the Southern Baikal volcanic area showed that they had similar contents of volatiles, major, and trace elements.  相似文献   

3.
High‐pressure granulites are generally characterized by the absence of orthopyroxene. However, orthopyroxene is reported in a few high‐pressure, felsic–metapelitic granulites, such as the Huangtuling felsic high‐pressure granulite in the North Dabie metamorphic core complex in east‐central China, which rarely preserves the high‐pressure granulite facies assemblage of garnet + orthopyroxene + biotite + plagioclase + K‐feldspar + quartz. To investigate the effects of bulk‐rock composition on the stability of orthopyroxene‐bearing, high‐pressure granulite facies assemblages in the NCKFMASHTO (Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–H2O–TiO2–Fe2O3) system, a series of P–T–X pseudosections based on the melt‐reintegrated composition of the Huangtuling felsic high‐pressure granulite were constructed. Calculations demonstrate that the orthopyroxene‐bearing, high‐pressure granulite facies assemblages are restricted to low XAl [Al2O3/(Na2O + CaO + K2O + FeO + MgO + Al2O3) < 0.35, mole proportion] or high XMg [MgO/(MgO + FeO) > 0.85] felsic–metapelitic rock types. This study also reveals that the XAl values in the residual felsic–metapelitic, high‐pressure granulites could be significantly reduced by a high proportion of melt loss. We suggest that orthopyroxene‐bearing, high‐pressure granulites occur in residual overthickened crustal basement under continental subduction–collision zones and arc–continent collision belts.  相似文献   

4.
The influence of melt composition and structure on the oxygen isotope fractionation was studied for the multicomponent (SiO2 ± TiO2 + Al2O3 ± Fe2O3 + MgO ± CaO) system at 1500°C and 1 atm. The experiments show that significant oxygen isotope effects can be observed in silicate melts even at such high temperature. It is shown that the ability of silicate melt to concentrate 18O isotope is mainly determined by its structure. In particular, an increase of the NBO/T ratio in the experimental glasses from 0.11 to 1.34 is accompanied by a systematic change of oxygen isotope difference between melt and internal standard by values from–0.85 to +1.29‰. The obtained data are described by the model based on mass-balance equations and the inferred existence of O0, O–, and O2– (bridging, non-bridging, and free oxygen) ions in the melts. An application of the model requires the intra-structure isotope fractionation between bridging and non-bridging oxygens. Calculations show that the intra-structure isotope fractionation in our experiments is equal to 4.2 ± 1.0‰. To describe the obtained oxygen isotope effects at the melts relatively to temperature and fraction of non-bridging oxygen a general equation was proposed.  相似文献   

5.
Stromatic metatexites occurring structurally below the contact with the Ronda peridotite (Ojén nappe, Betic Cordillera, S Spain) are characterized by the mineral assemblage Qtz+Pl+Kfs+Bt+Sil+Grt+Ap+Gr+Ilm. Garnet occurs in low modal amount (2–5 vol.%). Very rare muscovite is present as armoured inclusions, indicating prograde exhaustion. Microstructural evidence of melting in the migmatites includes pseudomorphs after melt films and nanogranite and glassy inclusions hosted in garnet cores. The latter microstructure demonstrates that garnet crystallized in the presence of melt. Re‐melted nanogranites and preserved glassy inclusions show leucogranitic compositions. Phase equilibria modelling of the stromatic migmatite in the MnO–Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–H2–O2–C (MnNCaKFMASHOC) system with graphite‐saturated fluid shows P–T conditions of equilibration of 4.5–5 kbar, 660–700 °C. These results are consistent with the complete experimental re‐melting of nanogranites at 700 °C and indicate that nanogranites represent the anatectic melt generated immediately after entering supersolidus conditions. The P–T estimate for garnet and melt development does not, however, overlap with the low‐temperature tip of the pure melt field in the phase diagram calculated for the composition of preserved glassy inclusions in garnet in the Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–H2O (NCKFMASH) system. A comparison of measured melt compositions formed immediately beyond the solidus with results of phase equilibria modelling points to the systematic underestimation of FeO, MgO and CaO in the calculated melt. These discrepancies are present also when calculated melts are compared with low‐T natural and experimental melts from the literature. Under such conditions, the available melt model does not perform well. Given the presence of melt inclusions in garnet cores and the P–T estimates for their formation, we argue that small amounts (<5 vol.%) of peritectic garnet may grow at low temperatures (≤700 °C), as a result of continuous melting reactions consuming biotite.  相似文献   

6.
Cordierite–orthoamphibole gneisses and rocks of similar composition commonly contain low‐variance mineral assemblages that can provide useful information about the metamorphic evolution of a terrane. New calculated petrogenetic grids and pseudosections are presented in the FeO–MgO–Al2O3–SiO2–H2O (FMASH), Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–H2O (NCKFMASH) and Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–H2O–TiO2–Fe2O3 (NCKFMASHTO) chemical systems to investigate quantitatively the phase relations in these rocks. Although the bulk compositions of cordierite–orthoamphibole gneisses are close to FMASH, calculations in this system do not adequately account for the observed range of mineral assemblages. Calculations in NCKFMASH and NCKFMASHTO highlight the role of minor constituents such as Ca, Na and Fe3+ in the mineral assemblage evolution of such rocks and these systems are more appropriate for interpreting the evolution of natural examples.  相似文献   

7.
Significant zonation in major, minor, trace, and volatile elements has been documented in naturally glassy olivine-hosted melt inclusions from the Siqueiros Fracture Zone and the Galapagos Islands. Components with a higher concentration in the host olivine than in the melt (e.g., MgO, FeO, Cr2O3, and MnO) are depleted at the edges of the zoned melt inclusions relative to their centers, whereas except for CaO, H2O, and F, components with a lower concentration in the host olivine than in the melt (e.g., Al2O3, SiO2, Na2O, K2O, TiO2, S, and Cl) are enriched near the melt inclusion edges. This zonation is due to formation of an olivine-depleted boundary layer in the adjacent melt in response to cooling and crystallization of olivine on the walls of the melt inclusions, concurrent with diffusive propagation of the boundary layer toward the inclusion center. Concentration profiles of some components in the melt inclusions exhibit multicomponent diffusion effects such as uphill diffusion (CaO, FeO) or slowing of the diffusion of typically rapidly diffusing components (Na2O, K2O) by coupling to slow diffusing components such as SiO2 and Al2O3. Concentrations of H2O and F decrease toward the edges of some of the Siqueiros melt inclusions, suggesting either that these components have been lost from the inclusions into the host olivine late in their cooling histories and/or that these components are exhibiting multicomponent diffusion effects. A model has been developed of the time-dependent evolution of MgO concentration profiles in melt inclusions due to simultaneous depletion of MgO at the inclusion walls due to olivine growth and diffusion of MgO in the melt inclusions in response to this depletion. Observed concentration profiles were fit to this model to constrain their thermal histories. Cooling rates determined by a single-stage linear cooling model are 150–13,000 °C h?1 from the liquidus down to ~1,000 °C, consistent with previously determined cooling rates for basaltic glasses; compositional trends with melt inclusion size observed in the Siqueiros melt inclusions are described well by this simple single-stage linear cooling model. Despite the overall success of the modeling of MgO concentration profiles using a single-stage cooling history, MgO concentration profiles in some melt inclusions are better fit by a two-stage cooling history with a slower-cooling first stage followed by a faster-cooling second stage; the inferred total duration of cooling from the liquidus down to ~1,000 °C ranges from 40 s to just over 1 h. Based on our observations and models, compositions of zoned melt inclusions (even if measured at the centers of the inclusions) will typically have been diffusively fractionated relative to the initially trapped melt; for such inclusions, the initial composition cannot be simply reconstructed based on olivine-addition calculations, so caution should be exercised in application of such reconstructions to correct for post-entrapment crystallization of olivine on inclusion walls. Off-center analyses of a melt inclusion can also give results significantly fractionated relative to simple olivine crystallization. All melt inclusions from the Siqueiros and Galapagos sample suites exhibit zoning profiles, and this feature may be nearly universal in glassy, olivine-hosted inclusions. If so, zoning profiles in melt inclusions could be widely useful to constrain late-stage syneruptive processes and as natural diffusion experiments.  相似文献   

8.
ABSTRACT

Silicate melt inclusions (SMIs) are small droplets of magma that become trapped in minerals during crystal growth. SMIs in olivine crystals can provide critical information on the range of melt compositions and processes that occur during melt generation, evolution, transport, and eruption. The Pliocene–Quaternary volcanic rocks in the Qorveh–Bijar volcanic belt of western Iran show porphyritic and microlithic textures, with olivine and clinopyroxene being the dominant minerals. Magnesian olivines in these volcanic rocks contain primary SMIs. The composition and characteristic of olivine-hosted SMI of these rocks are investigated to constrain the source lithology for mafic volcanism. Bulk compositions of the SMIs overlap those of their host rocks and extend to higher CaO/Al2O3 values. The estimated entrapment pressures and temperatures of the studied SMIs are 9.1–10.3 kbar and 1220–1355°C. The calculated mafic parental melt contains 42.36 wt.% SiO2, low total alkalis (3.22 wt.%), and high MgO (16.1 wt.%). Exploratory calculations using pMELTS show that this parental composition underwent variable degrees of fractional crystallization, as reflected by the variable compositions of the SMIs. Several lines of evidence including pyroxene xenocrysts and high FeO/MnO, FC3MS (FeO/CaO – 3*MgO/SiO2), and Zn/Fe ratios (14–21), suggest that a metasomatized pyroxenitic source contributed to the genesis of the parental melt. Amphibole in the SMIs indicates a high volatile content in the parental melt, which we conclude was generated from a metasomatized lithospheric mantle source. The pyroxenite source also contained garnet. Our geochemical results lead us to propose a new petrogenetic model. Specifically, we infer that a dense and unstable portion of the lithosphere underwent localized laminar detachment and downward flow, i.e. lithospheric drip. This drip underwent volatile-enhanced partial melting during descent through the underlying hot asthenosphere and generated the studied volcanic rocks.  相似文献   

9.
The equilibrium coexistence of sapphirine + quartz is inferred to record temperatures in excess of 980 °C, based on the stability of this assemblage in the simplified chemical system FeO–MgO–Al2O3–SiO2 (FMAS) system. However, the potential for sapphirine to contain significant Fe3+ suggests that the stability of sapphirine + quartz could extend to lower temperatures than those constrained in this ideal system. The Wilson Lake terrane in the Grenville Province of central Labrador preserves sapphirine + quartz‐bearing assemblages in highly oxidized bulk compositions, and provides an opportunity to explore the stability of sapphirine + quartz in such rock compositions within the Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–H2O–TiO2–O (NCKFMASHTO) chemical system. Starting with the phase equilibria in FeO–MgO–Al2O3–SiO2–TiO2–O (FMASTO), expansion into K2O–FeO–MgO–Al2O3–SiO2–H2O–TiO2–O (KFMASHTO) allows the effect of the stability of the additional phases, biotite, K‐feldspar and melt, on the stability of sapphirine + quartz to be assessed. These phase relations are evaluated generally using P–T projections, and the ultimate extension into NCKFMASHTO is done with pseudosections. Conditions of peak metamorphism in the Wilson Lake terrane are constrained using P–T pseudosections, and the appropriate H2O and O contents to use in the modelled compositions are investigated using T–MH2O and T–MO pseudosections. The peak P–T estimates from a sapphirine + quartz‐bearing sample are ～960 to 935 °C at ～10 to 8.6 kbar, similar to estimates from orthopyroxene + sillimanite + quartz ± garnet‐bearing samples. Whereas the sapphirine + quartz‐bearing sample is more Fe‐rich than the orthopyroxene + sillimanite‐bearing sample on an all‐Fe‐as‐FeO basis, once the oxidation state is taken into account, the former is effectively more magnesian than the latter, accounting for the sapphirine occurrence.  相似文献   

10.
Principal components analysis is used to study the chemical compositions of pyroxenes of five Apollo 12 specimens. Important correlations recognized in the variation of oxide weight per cent are: MGO, Al2O3, SiO2| CaO, TiO2, FeO MgO, Al2O3, SiO2| FeO MgO, SiO2, FeO | Al2O3, CaO, TiO2 where the oxides on one side of the bar are correlated positively with each other and negatively with the oxides on the other side. Several other similarly distinct relationships with significantly less variance could be noted. These correlations indicating substitutional relationships can be interpreted as representative of stable and metastable trends of crystallization by using crystal-chemical and thermodynamic information. The per cent variance of pyroxene groups with characteristic trends in each specimen can be evaluated and interpreted in terms of history of crystallization. Distribution of Fe and Mg in certain pairs of olivine and pyroxene, which are found in contact in the rock and which may have crystallized simultaneously, is useful in recognizing the tendency towards chemical equilibrium in FeMg distribution during a limited interval in the liquidus or subsolidus stages.  相似文献   

11.
Mid-ocean ridge basalts (MORBs) from East Pacific Rise (EPR) 13°N are analysed for major and trace elements, both of which show a continuous evolving trend. Positive MgO–Al2O3 and negative MgO–Sc relationships manifest the cotectic crystallization of plagioclase and olivine, which exist with the presence of plagioclase and olivine phenocrysts and the absence of clinopyroxene phenocrysts. However, the fractionation of clinopyroxene is proven by the positive correlation of MgO and CaO. Thus, MORB samples are believed to show a “clinopyroxene paradox”. The highest magnesium-bearing MORB sample E13-3B (MgO=9.52%) is modelled for isobaric crystallization with COMAGMAT at different pressures. Observed CaO/Al2O3 ratios can be derived from E13-3B only by fractional crystallization at pressure >4 ±1 kbar, which necessitates clinopyroxene crystallization and is not consistent with cotectic crystallization of olivine plus plagioclase in the magma chamber (at pressure ~1 kbar). The initial compositions of the melt inclusions, which could represent potential parental magmas, are reconstructed by correcting for post-entrapment crystallization (PEC). The simulated crystallization of initial melt inclusions also produce observed CaO/Al2O3 ratios only at >4±1 kbar, in which clinopyroxene takes part in crystallization. It is suggested that MORB magmas have experienced clinopyroxene fractionation in the lower crust, in and below the Moho transition zone. The MORB magmas have experienced transition from clinopyroxene+plagioclase+olivine crystallization at >4±1 kbar to mainly olivine+plagioclase crystallization at <1 kbar, which contributes to the explanation of the “clinopyroxene paradox”.  相似文献   

12.
Stability of phengite and biotite in eclogite is discussed using petrological data of natural eclogites, and the observational data are examined by thermodynamic calculations. Generally, phengite is a major K phase in natural eclogite and is stable in wide range of bulk composition. However, in eclogites from several localities of the Caledonides, biotite occurs as a stable eclogite-facies mineral, and is often associated with orthopyroxene. Bulk compositions of such biotite- or orthopyroxene-bearing eclogites are compared with those of eclogites from the Dabie–Sulu region, China, where phengite is a major K phase in eclogite. The biotite- or orthopyroxene-bearing eclogites from the Western Gneiss Region of the Caledonides are rich in MgO (10–15 wt%) and relatively poor in CaO (7–8 wt%) and Al2O3 (12–16 wt%). The CaO/MgO ratios of the biotite- or orthopyroxene-bearing eclogites are clearly lower than those of eclogites from the Dabie–Sulu region, indicating that MgO-rich and CaO-poor environments should be important for stabilizing of biotite and orthopyroxene in eclogite. Biotite-bearing eclogite from the North-East Greenland Eclogite Province is rich in MgO (≈16 wt%) and CaO (≈15.5 wt%) and extremely poor in Al2O3 (≈8 wt%). To stabilize biotite in eclogite, Al2O3-poor environments are also important. Bulk compositions of these biotite- or orthopyroxene-bearing eclogites are similar to picrite basaltic compositions. To examine these observational data, thermodynamic calculations were carried out in a seven-component system KH2O1.5–Na2O–CaO–FeO–MgO–Al2O3–SiO2, which includes garnet, kyanite, phengite, biotite, quartz, omphacite, orthopyroxene and olivine in conjunction with mass-balance calculations. Firstly, calculations were performed on the average bulk composition of eclogites from the Dabie–Sulu region to lherzolite (KLB-1). The calculation results confirmed that phengite should be stable in eclogite with 'ordinary' basaltic composition, whereas biotite and orthopyroxene should be stable in picrite basaltic compositions (e.g. MgO >11.0 wt%, CaO <9.8 wt%, Al2O3 <15.2 wt% at 700 °C, 2.5 GPa). Further calculations in basaltic system confirmed that increase of MgO content and decrease of CaO and Al2O3 contents were important to stabilize biotite and orthopyroxene in eclogite. Thus, mineral assemblage in picrite basalt system should be completely different from that in normal basaltic system.  相似文献   

13.
A new zonation type of W–Mo-bearing altered biotite hornfels at the Tyrnyauz deposit is reported. The review of zonation indicates a subsequent transition into the mobile state of CaO, MgO, FeO, and Al2O3 and retention of volume owing to dissolution or deposition of quartz as an excess mobile mineral. The main features of zonation are similar to those in acid leaching columns; the input of strong CaO base into the outer zone is unusual.  相似文献   

14.
The Neoarchean Bundelkhand greenstone sequences at Mauranipur and Babina areas within the Bundelkhand Gneissic Complex preserve a variety of magmatic rocks such as komatiitic basalts, basalts,felsic volcanic rocks and high-Mg andesites belonging to the Baragaon, Raspahari and Koti Formations.The intrusive and extrusive komatiitic basalts are characterized by low SiO_2(39-53 wt.%), high MgO(18-25 wt.%).moderately high Fe_2O_3(7.1-11.6 wt.%), Al_2O_3(4.5-12.0 wt.%), and TiO_2(0.4-1.23 wt.%)with super to subchondritic(Gd/Yb)N ratios indicating garnet control on the melts. The intrusive komatiitic suite of Ti-enriched and Al-depleted type possesses predominant negative Eu and positive Nb, Ti and Y anomalies. The chemical composition of basalts classifies them into three types with varying SiO_2, TiO_2, MgO, Fe_2O_3, Al_2O_3 and CaO. At similar SiO_2 content of type Ⅰ and Ⅲ basalts, the type II basalts show slightly high Al_2O_3 and Fe_2O_3 contents. Significant negative anomalies of Nb, Zr, Hf and Ti, slightly enriched LREE with relatively flat HREE and low ∑REE contents are observed in type Ⅰ and Ⅱ basalts. TypeⅢ basalts show high Zr/Nb ratios(9.8-10.4), TiO_2(1.97-2.04 wt.%), but possess strikingly flat Zr, Hf, Y and Yb and are uncontaminated. Andesites from Agar and Koti have high SiO_2(55-64 wt.%), moderate TiO_2(0.4-0.7 wt.%), slightly low Al_2O_3(7-11.9 wt.%), medium to high MgO(3-8 wt.%) and CaO contents(10-17 wt.%). Anomalously high Cr, Co and Ni contents are observed in the Koti rhyolites. Tholeiitic to calc alkaline affinity of mafic-felsic volcanic rocks and basalt-andesite dacite-rhyolite differentiation indicate a mature arc and thickened crust during the advanced stage of the evolution of Neoarchean Bundelkhand greenstone belt in a convergent tectonic setting where the melts were derived from partial melting of thick basaltic crust metamorphosed to amphibolite-eclogite facies. The trace element systematics suggest the presence of arc-back arc association with varying magnitudes of crust-mantle interaction. La/Sm, La/Ta,Nb/Th, high MgO contents(20 wt.%), CaO/Al_2O_3 and(Gd/Yb)_N 1 along with the positive Nb anomalies of the komatiite basalts reflect a mantle plume source for their origin contaminated by subductionmetasomatized mantle lithosphere. The overall geochemical signatures of the ultramafic-mafic and felsic volcanic rocks endorse the Neoarchean plume-arc accretion tectonics in the Bundelkhand greenstone belt.  相似文献   

15.
The chemical compositions of tephra shards are widely utilised in a myriad of disciplines, including volcanology, petrology, tephrochronology, palaeoecology and climate studies. Previous research has raised concerns over the possible chemical alteration of microscopic (<100 µm) volcanic glass shards through standard extraction procedures, such as the widely used acid digestion method. This study subjects 10 samples of well‐characterised volcanic glasses ranging from basalt to rhyolite to three common methods used in the extraction of volcanic material from lake sediments and peats. The major element geochemistry of each sample was analysed and compared with a control group. The results of this test indicate that basaltic and andesitic glasses are highly susceptible to chemical alteration, particularly to the concentrated corrosive materials used in acid and base digestion techniques. PERMANOVA analysis of the variation within groups suggests that the oxides most susceptible to variation are alkalis from groups I and II (K2O, Na2O, CaO, MgO) and SiO2, and the most stable oxides are Al2O3 and FeO. Felsic glasses are considerably less susceptible to alteration by both acidic (HCl, HNO3, H2SO4) and alkaline (KOH) digestions. Our findings have important implications for interpreting the geochemistry of volcanic glasses. Copyright © 2019 John Wiley & Sons, Ltd.  相似文献   

16.
Progress relating to calculation of partial melting equilibria for metapelites   总被引：36，自引：4，他引：32  
Improved activity–composition relationships for biotite, garnet and silicate liquid are used to construct updated P–T grids and pseudosections for high‐grade metapelites. The biotite model involves Ti charge‐balanced by hydrogen deprotonation on the hydroxyl site, following the substitution , where HD represents the hydroxyl site. Relative to equivalent biotite‐breakdown melting reactions in P–T grids in K2O–FeO–MgO–Al2O3–SiO2–H2O (KFMASH), those in K2O–FeO–MgO–Al2O3–SiO2–H2O–TiO2–O2 (KFMASHTO) occur at temperatures close to 50 °C higher. A further consequence of the updated activity models is that spinel‐bearing equilibria occur to higher temperature and higher pressure. In contrast, the addition of Na2O and CaO to KFMASH to make the Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–H2O (NCKFMASH) system lowers key biotite‐breakdown melting reactions in P–T space relative to KFMASH. Combination of the KFMASHTO and NCKFMASH systems to make Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–H2O–TiO2–O2 (NCKFMASHTO) results in key biotite‐breakdown melting reactions occurring at temperatures intermediate between those in KFMASHTO and those in NCKFMASH. Given such differences, the choice of model system will be critical to inferred P–T conditions in the application of mineral equilibria modelling to rocks. Further, pseudosections constructed in KFMASH, NCKFMASH and NCKFMASHTO for several representative rock compositions show substantial differences not only in the P–T conditions of key metamorphic assemblages but also overall topology, with the calculations in NCKFMASHTO more reliably reflecting equilibria in rocks. Application of mineral equilibria modelling to rocks should be undertaken in the most comprehensive system possible, if reliable quantitative P–T information is to be derived.  相似文献   

17.
A. A. Borisov 《Petrology》2009,17(6):579-590
The simultaneous saturation of silicate melts with variable Al2O3 and SiO2 contents in sodium, potassium, and rubidium was investigated at a total pressure of 1 atm and temperatures of 1300–1470°C using the crucible supported loop technique. It was shown that an increase in both SiO2 and Al2O3 contents in the melt results in a significant decrease in the activity coefficients of the alkalis, and the effect of Al2O3 is especially pronounced in silicic compositions. The extrapolation of the experimental data allowed us to estimate the influence of SiO2 and Al2O3 contents in the melt on the behavior of Li and Cs. Using a numerical experiment, it was shown how the inert and perfectly mobile behavior of alkalis in magmatic processes can be discriminated. A methodic investigation was performed on the loss of Na, K, and Rb from silicic glasses during microprobe analysis depending on beam diameter.  相似文献   

18.
黔北务川瓦厂坪铝土矿床元素迁移规律研究   总被引：6，自引：0，他引：6  
金中国 《地质与勘探》2011,47(6):957-966
黔北务正道地区铝土矿矿床属古风化壳沉积型,成矿母岩具多源性,但主要来源于下覆的中下志留统韩家店组。本文依据Grant提出的质量平衡方程和图解法,对瓦厂坪矿床在成矿过程中元素迁移的富集、贫化（亏损）规律进行了定量研究。结果表明,主要成矿母岩韩家店组砂、页岩一中间产物铝土质页岩、粘土岩是主要元素A12O3、TiO2显著富集...  相似文献   

19.
The present study attempted to evaluate the influence of human activity on major elements (Na2O, MgO, Al2O3, SiO2, K2O, CaO, Fe2O3), and to find a method to explore correlations between major elements and human disturbances, according to geospatial theories and methods. The study results indicate that landscapes influence major elements in diverse ways: Al2O3 is closely related to road and mine landscapes; strong relationships exist between MgO, Fe2O3, CaO, and SiO2 and roads; Na2O, SiO2, and Fe2O3 are unrelated to city landscapes; and Na2O is unrelated to road and mine landscapes.  相似文献   

20.
Crystalline and melt inclusions were studied in large (up to 2 cm across) dipyramidal quartz phenocrysts from Miocene dacites in the area of the Rosia Montana Au-Ag deposit in Romania. Data were obtained on the homogenization of fluid inclusions and the composition of crystalline inclusions and glasses in more than 40 melt inclusions, which were analyzed on a electron microprobe. The minerals identified in the crystalline inclusions are plagioclase (An 51–62), orthoclase, micas (biotite and phengite), zircon, magnetite (TiO2 = 2.8 wt %), and Fe sulfide. Two types of the melts were distinguished when studying the glasses of the melt inclusions. Type 1 of the melts is unusual in composition. The average composition of 20 inclusions is as follows (wt %): 76.1 SiO2, 0.39 TiO2, 6.23 Al2O3, 4.61 FeO, 0.09 MnO, 1.64 MgO, 3.04 CaO, 2.79 Na2O, 3.79 K2O (Na2O/K2O = 0.74), 0.07 P2O5, 0.02 Cl. The composition of type 2 of the melts is typical of acid magmas. The average of 23 inclusion analyses is (wt %) 79.3 SiO2, 0.16 TiO2, 10.27 Al2O3, 0.63 FeO, 0.08 MnO, 0.29 MgO, 1.83 CaO, 3.56 Na2O, 2.79 K2O (Na2O/K2O = 1.28), 0.08 P2O5, 0.05 Cl. The compositions of these melts significantly differ in concentrations of Ti, Al, Fe, Mg, Ca, Na, and K. The high analytical totals of the analyses (close to 100 wt %, more specifically 98.9 and 99.0 wt %, respectively) testify that the melts were generally poor in water. Two inclusions of type 1 and two inclusions of type 2 were analyzed on an ion probe, and their analyses show remarkable differences in the concentrations of certain trace elements. These concentrations (in ppm) are for the melts of types 1 and 2, respectively, as follows: 10.0 and 0.69 for Be, 29.3 and 5.7 for B, 6.4 and 1.4 for Cr, 146 and 6.9 for V, 74 and 18 for Cu, 92 and 29 for Rb, 45 and 15 for Zr, 1.7 and 0.6 for Hf, 10.3 and 2.3 for Pb, and 52 and 1.3 for U. The Th/U ratio of these two melt types are also notably different: 0.04 and 0.19 for type 1 and 2.0 and 2.9 for type 2. These data led us to conclude that the magmatic melts were derived from two different sources. Our data on the melts of type 1 testify that the magmatic chamber was contaminated with compositionally unusual crustal rocks (perhaps, sedimentary, metamorphic, or hydrothermal rocks enriched in Si, Fe, Mg, U, and some other components). This can explain the ore-forming specifics of magmatic chambers in the area.  相似文献   

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