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1.
W. Johannes 《Contributions to Mineralogy and Petrology》1979,68(2):221-230
The ternary feldspar system KAlSi3O8 - NaAlSi3O8 - CaAl2Si2O8 was reinvestigated at 650 ° C and 800 ° C (P H2O = 1 kb) using mixtures of crystalline plagioclases and alkali feldspars as starting materials. The compositions of plagioclases and alkali feldspars of the run products were determined by X-ray means. The Or-content of the feldspar phases was determined by measuring the position of the (201) X-ray peak of the unexchanged feldspars, whereas the An-content was determined by measuring the same X-ray peak of the K-exchanged feldspars. The reaction rate of a reaction leading to a more An-rich plagioclase (type II reaction) is much faster than a reaction producing a more Ab-rich plagioclase (type I). In a type II reaction run times of approximately 20 days are needed to reach new constant plagioclase and alkali feldspar compositions at 650 ° C, and 10 days are needed to reach constant compositions at 800 ° C. In a reaction of type I only the outer zone of the plagioclases reacts to more Abrich compositions. A diffuse zone with a wide range of compositions was observed in 650 ° C runs. Equilibrium could not be reached in these experiments within 45 days. At 800 ° C a new zone having a specific composition develops in 42 days. This new zone is believed to be in equilibrium with the coexisting alkali feldspar. The depth of reaction is calculated as 0.03 μm after 42 days (800 ° C, P f= 1 kb). The reaction between the two feldspar phases could be reversed at 800 ° C. The following compositions are considered to represent equilibrium data at 800 ° C and P t = 1 kb: An 43 Ab 51 Or 6 coexisting with Or 79 Ab 20 An 1, and An 40 Ab 54 Or 6 coexisting with Or 75 Ab 24 An 1. Recent data obtained with gels of ternary feldspar composition as starting materials do not agree with the results presented in this paper. Gels obviously crystallize spontaneously forming coexisting feldspars of non - equilibrium composition - alkali feldspars too rich in Ab and plagioclases too rich in An. 相似文献
2.
Mark S. Ghiorso 《Contributions to Mineralogy and Petrology》1987,96(3):291-313
Lasaga's (1982) Master Equation for crystal growth is solved for multicomponent systems in situations which allow for coupled diffusion of melt species. The structure of the solution is explored in some detail for the case of a constant diffusion coefficient matrix. Incorporating these results, the growth of plagioclase is modeled in undercooled tholeiitic melts by approximating interface growth rates with (1) a reduced growth rate function and with (2) calculated solid-liquid solution properties obtained from the silicate liquid solution model of Ghiorso et al. (1983; appendix of Ghiorso 1985). For this purpose algorithms are provided for estimating the liquidus temperature or the chemical affinity of a multicomponent solid solution precipitating from a complex melt of specified bulk composition. Compositional trends in initial solids produced by successive degrees of undercooling are opposite to those predicted in the binary system NaAlSi3O8-CaAl2Si2O8. Calculations suggest that the solid phase and interface melt compositions rapidly approach a steady state for a given degree of undercooling. Consequently, the overall isothermal growth rate of plagioclase forming from tholeiitic melts appears to be entirely diffusion controlled. In magmatic systems the multicomponent growth equations allow for the formation of oscillatory zoned crystals as a consequence of the couplingr between interface reaction kinetics and melt diffusion. The magnitude of this effect is largely dependent upon the asymmetry of the diffusion coefficient matrix. Methods are described to facilitate the calibration of diffusion matrices from experimental data on multicomponent penetration curves.Experimental results (Lesher and Walker 1986) on steady state Soret concentration profiles resulting from thermal diffusion in MORB and andesitic liquids are analyzed using the theory of multicomponent linear irreversible thermodynamics. Under conditions where the entropy production is minimized, a linear relationship is derived between liquid chemical potentials and temperature. This relationship is utilized to evaluate the validity of the solution model of Ghiorso et al. (1983) in melts up to 300° C above their liquidus. The results indicate that configurational entropies are accurately modeled for MORB and andesite bulk compositions. The modeling fails in two four-component systems tested. Equations are derived which allow the calibration of multicomponent regular solution parameters from steady state Soret arrays. An algorithm is demonstrated which permits the calculation of steady state Soret concentration profiles, given an overall bulk melt composition and temperature gradient. This algorithm uses the liquid solution properties of Ghiorso et al. (1983) and constants obtained from the experimental measurements of Lesher and Walker (1986). 相似文献
3.
Garnet and plagioclase pairs from fourteen selected samples, from garnet to sillimanite zones, collected along a NS traverse throughout the metamorphic basement of NE Sardinia, have been analyzed by microprobe.Beyond the garnet isograd, plagioclase has albitic composition and the garnet (a Ca-rich almandine) shows Ca/ Ca+Mg+Fe ratios of about 0.35–0.30, fairly constant from core to rim.Towards the North, still in the garnet zone, when on the large albitic core of plagioclase a thin and discontinuous oligoclasic rim (An22–An18) formed, we observe in the garnet edge an abrupt decrease of the Ca/Ca+Mg+Fe ratio (0.27–0.16).In the staurolite and sillimanite zones garnet does not show significant Ca-zoning and it is characterized by low Ca content (Ca/Ca+Mg+Fe<0.1); the coexisting plagioclase has oligoclasic (An16–An27) composition.The chemical data and the microstructural evidence on growth time indicate that the garnet and plagioclase had a strong mutual interference in determining the relative Ca distribution.The most relevant reactions are discussed and, in particular, the antipathetical Ca-zoning, recorded by garnet and plagioclase in the garnet zone, is considered as the evidence of temperature increase during growth of the two minerals. It is also suggested that the sharp variation of Ca content at the garnet edge was controlled by the discontinuous nature of plagioclase solid solution in the peristeritic range.The order of appearance of garnet and oligoclase in the basement of NE Sardinia is also discussed in comparison with other well known metamorphic sequence (Vermont, New Zealand and Dalradian). It is concluded that the different order of appearance is controlled other than the different nature of the calcic phases in the lower grade zones also by the
in the fluid phase. 相似文献
4.
Feldspar chemical variations in representative leucite-bearing and related rocks from well-known localities in Italy, Germany, Uganda and Australia demonstrate that phenocrystal core to rim variations may not represent the feldspar crystallization trend in the host lava and only the groundmass feldspar zoning trend is a reliable indicator of crystal-liquid relationships. Textural relationships indicate that coexisting plagioclase and alkali feldspar crystallized sequentially, the latter after the former, rather than cotectically.Groundmass alkali feldspar show Ca-, Na-depletion and K-enrichment zoning trends. Plagioclase crystallization follows Ca-depletion, Na and K-enrichment trends. Typically, Sr and Ba solid solubility is significant, particularly in groundmass feldspar.The alkali feldspar variation trend from groundmass assemblages is not consistent with the theoretical phase relationships in the system NaAlSiO4-KAlSiO4 CaAl2Si2O8-SiO2 (The phonolite pentahedron) proposed by Carmichael et al. (1974).Factors believed to be important in controlling feldspar crystallization trends are the Sr-Ba feldspar components, the role of the coexisting pyroxene and the presence of F, Cl and/or their alkali compounds. 相似文献
5.
Feldspathic hornblende and garnet granulites and associated anorthosite pegmatites from Doubtful Sound,Fiordland, New Zealand 总被引：3，自引：0，他引：3
G. J. H. Oliver 《Contributions to Mineralogy and Petrology》1977,65(2):111-121
Feldspathic hornblende granulites from Doubtful Sound, New Zealand with the assemblage plagioclase+hornblende+clinopyroxene+orthopy-roxene +oxide+apatite are criss-crossed by a network of garnetiferous anorthosite veins and pegmatites. The feldspathic gneiss in contact with anorthosite has a reaction zone containing the assemblage plagioclase +garnet+clinopyroxene+quartz+rutile+apatite. The garnet forms distinctive coronas around clinopyroxene. The origin of these rocks is discussed in the light of mineral and whole rock chemical analyses and published experimental work.It is thought that under conditions leading up to 750 °C, 8 kb load pressure and 5 kb H2O pressure, partial melting occured in feldspathic hornblende granulites. The melt migrated into extensional fractures and eventually crystallised as anorthosite pegmatites and veins. The gneisses adjacent to the pegmatites from which the melt was extracted changed composition slightly, by the loss of H2O and Na2O, so that plagioclase reacted simultaneously with hornblende, orthopyroxene, and oxide to form garnet, clinopyroxene, quartz and rutile. 相似文献
6.
Partition of Fe2+ and Mg between coexisting (Mg, Fe)2SiO4 spinel and (Mg, Fe)SiO3 pyroxene was investigated at pressures 80 and 90 kbar and at temperatures 840 and 1050° C, using tetrahedral-anvil type of high pressure apparatus. Olivine-spinel solid solution equilibria in the system Mg2SiO4-Fe2SiO4 were discussed in the light of the partition reaction. Partition of Fe2+ and Mg in both olivine-spinel and pyroxene-spinel systems can not be regarded as that between ideal solid solutions. By applying the simple solution model for the partition of Fe2+ and Mg, sign of the heat of mixing was estimated to be positive for all olivine, spinel and pyroxene. Relative concentration of Fe2+ in spinel in the pyroxene-spinel system is likely to cause some change in the chemical composition of modified spinel () or spinel () in the transition zone of the mantle. A considerable change is also expected in the transition pressure of to ( + ) and ( + ) to .Presented at the symposium Recent Advances in the Studies of Rocks and Minerals at High Pressures and Temperatures held in Montreal, 1972. Jointly sponsored by the International Mineralogical Association and the Commission on Experimental Petrology. 相似文献
7.
Dr. K. Mereiter 《Mineralogy and Petrology》1979,26(4):279-292
Summary The crystal structure of curite, of which until now only the arrangement of the U and Pb atoms was known, has been redetermined with a synthetic crystal using three-dimensional X-ray techniques.R=0.043 for 1270 observed reflections. Curite is orthorhombic, space groupPnam-D
2h
16
,a=12.513,b=13.002,c=8.373 ,Z=6.56 PbO·16UO3·9.44H2O. The structure consists of a novel type of washboard like puckered layers
2
[(UO2)8O8 (OH)6]6– formed by tetragonal bipyramidal [(UO2)O3(OH)] and pentagonal bipyramidal [(UO2)O3 (OH)2] polyhedra. The layers are parallel to {100} and are directly connected by hydrogen bonds. Lead atoms and oxygen atoms (H2O+OH) are located in folds between the layers, helping to connect them. The interlayer atomic positions are slightly disordered and one of them is partially occupied. The variable concentrations of the interlayer atoms are responsible for the changes in chemical composition.The structural formula [Pb8–x
(OH)4–2x
(H2O)2x
] [(UO2)8(OH)6]2 is suggested for curite;x=1.44 for the investigated synthetic curite. Within the three different U–O polyhedra the axial U–O distances are 1.81–1.88 , the equatorial 2.14–2.57 . The two different Pb atoms have ionic coordinations, each by ten oxygens with Pb–O distances of 2.46–3.32 , on the average 2.82 .
With 3 Figures 相似文献
Die Kristallstruktur von Curit, [Pb 6,56 (H 2 O, OH) 4 ] [(UO 2)8 O 8(OH)6]2
Zusammenfassung Die Kristallstruktur von Curit, von der bisher nur die Lagen der Uran- und Bleiatome bekannt waren, wurde anhand eines künstlichen Kristalls mit dreidimensionalen Röntgendaten neu bearbeitet und für 1270 Reflexe aufR=0,043 verfeinert. Curit kristallisiert rhombisch, RaumgruppePnam-D 2h 16 ,a=12,513,b=13,002,c=8,373 ,Z=6,56 PbO·16 UO3·9,44 H2O. Die Struktur enthält gewellte Schichten eines neuen Typs, 2 [(UO2)8O8(OH)6]6–, die sich aus tetragonal bipyramidalen [(UO2)O3(OH)]- und pentagonal-bipyramidalen [(UO2)O3(OH)2]-Polyedern zusammensetzen. Die Schichten verlaufen parallel {100} und sind über Wasserstoffbrücken miteinander unmittelbar verknüpft. Zwischen den Schichten befinden sich Bleiatome und zusätzliche Sauerstoffatome (H2O+OH). Diese Atome weisen zum Teil Fehlordnung auf; eine der beiden Pb-Lagen ist nur partiell besetzt. Für Schwankungen in der chemischen Zusammensetzung von Curit ist der unterschiedliche Gehalt an Zwischenschichtatomen verantwortlich. Aufgrund dieser Untersuchung wird die Strukturformel [Pb8–x (OH)4–2x (H2O)2x ] [(UO2)8O8(OH)6]2 vorgeschlagen; für den untersuchten Curit istx=1,44. Die drei verschiedenen U–O-Polyeder der Struktur besitzen axiale bzw. äquatoriale U–O-Abstände von 1,81–1,88 bzw. 2,14–2,57 . Die zwei Arten von Bleiatomen besitzen eine ionische Koordination; beide sind von 10 Sauerstoffatomen in Abständen von 2,46–3,32 (Mittelwert 2,82 ) umgeben.
With 3 Figures 相似文献
8.
The syenitic layered series in the Klokken intrusion is surrounded by a zone (500 m thick) of nearly structureless unlaminated syenite followed outwards by a zone of vertically banded gabbro (200 m thick) at the outer rim. The unlaminated syenite is intrusive into the gabbro and develops a thin (2 m) transition zone of syenodiorite at the contact. A traverse across the vertical transition zone and inwards towards the layered series was sampled with a portable drill. Mafic silicates (olivine, clinopyroxene, biotite) show inward evolution in Fe/(Fe+Mg) across the syenodiorite-unlaminated syenite zones. Feldspars change rapidly across the syenodiorite zone from rocks dominated by plagioclase, in some cases together with two alkali feldspars, one a mesoperthite or cryptomesoperthite, the other a cryptoperthite, to rocks in which plagioclase is seen only rarely as cores to cryptomesoperthitic alkali feldspar crystals. Plagioclase is absent from the layered series.Alkali feldspars occurring in pairs have bulk compositions on solvus isotherms in the Or-Ab-An ternary system, estimated at 950° C in a syenogabbro and 910° C in a syenodiorite, at 1 kbar. The more calcic liquids from which they crystallized fractionated on paths that intersected the two- feldspar surface, whereas the more syenitic members crystallized from liquids which terminated crystallization in the one- feldspar field at 900° C. Plagioclases evolve from calcic andesine in syenodiorites, to very rare sodic oligoclase in the most evolved unlaminated syenites. The boundaries between plagioclase cores and alkali feldspar rims, which are usually optically abrupt, involve complex mixed zones on the m -scale, consistent with arrested reaction between plagioclase primocrysts and crystallizing syenitic liquid. Ternary liquidus-solidus relationships are in qualitative agreement with this interpretation. The syenodiorites are cumulates produced during sidewall crystallization of a trachytic magma against a gabbroic chamberlining. This magma changed little in bulk composition as it evolved, giving rise to the unlaminated syenites by further sidewall crystallization. Water build- up in this liquid probably caused a change in style of chamber filling, giving rise to the layered series by bottom accumulation. Microtextures in the zoned feldspars are described in an accompanying paper.CRPG contribution 729 相似文献
9.
Mark S. Ghiorso 《Contributions to Mineralogy and Petrology》1990,104(6):645-667
A solution model is developed for rhombohedral oxide solid solutions having compositions within the ternary system ilmenite [(Fe
2+
s
Ti
4+
1–s
)
A
(Fe
2+
1–s
Ti
4+
s
)
B
O3]-geikielite [(Mg
2+
t
Ti
4+
1–t
)
A
(Mg
2+
1–t
Ti
4+
t
)
B
O3]-hematite [(Fe3+)
A
(Fe3+)
B
O3]. The model incorporates an expression for the configurational entropy of solution, which accounts for varying degrees of structural long-range order (0s, t1) and utilizes simple regular solution theory to characterize the excess Gibbs free energy of mixing within the five-dimensional composition-ordering space. The 13 model parameters are calibrated from available data on: (1) the degree of long-range order and the composition-temperature dependence of the
transition along the ilmenite-hematite binary join; (2) the compositions of coexisting olivine and rhombohedral oxide solid solutions close to the Mg–Fe2+ join; (3) the shape of the miscibility gap along the ilmenite-hematite join; (4) the compositions of coexisting spinel and rhombohedral oxide solid solutions along the Fe2+–Fe3+ join. In the course of calibration, estimates are obtained for the reference state enthalpy of formation of ulvöspinel and stoichiometric hematite (–1488.5 and –822.0 kJ/mol at 298 K and 1 bar, respectively). The model involves no excess entropies of mixing nor does it incorporate ternary interaction parameters. The formulation fits the available data and represents an internally consistent energetic model when used in conjuction with the standard state thermodynamic data set of Berman (1988) and the solution theory for orthopyroxenes, olivines and Fe–Mg titanomagnetite-aluminate-chromate spinels developed by Sack and Ghiorso (1989, 1990a, b). Calculated activity-composition relations for the end-members of the series, demonstrate the substantial degree of nonideality associated with interactions between the ordered and disordered structures and the dominant influence of the miscibility gap across much of the ternary system. The predicted shape of the miscibility gap, and the orientation of tie-lines relating the compositions of coexisting phases, display the effects of coupling between the excess enthalpy of solution and the degree of long-range order. One limb of the miscibility gap follows the composititiontemperature surface corresponding to the ternary
second-order transition. 相似文献
10.
Myrmekite, as defined here, is the microscopic intergrowth between vermicular quartz and modestly anorthitic plagioclase (calcic albite-oligoclase), intimately associated with potassium feldspar in plutonic rocks of granitic composition. Hypotheses previously invoked in explanation of myrmekite include: (1) direct crystallization; (2) replacement; (3) exsolution. The occurrence of myrmekite in paragneisses and its absence in rocks devold of discrete grains of potassium feldspar challenge those hypotheses based on direct crystallization or replacement. However, several lines of evidence indicate that myrmekite may in fact originate in response to kinetic effects associated with the exsolution of calcic alkali feldspar into discrete potassium feldspar and plagioclase phases. Exsolution of potassium feldspar system projected from [AlSi2O8] involves the exchange CaAlK-1Si-1, in which the AlSi-1 tetrahedral couple is resistant to intracrystalline diffusion. By contrast, diffusion of octahedral K proceeds relatively easily where it remains uncoupled to the tetrahedral exchange. We suggest here that where the ternary feldspar system is open to excess silica, the exchange reaction that produces potassium feldspar in the ternary plane is aided by the net-transfer reaction K+Si=Orthoclase, leaving behind indigenous Si that reports as modal quartz in the evolving plagioclase as the CaAl component is concomitantly incorporated in this same phase. Thus silica is pumped into the reaction volume from a silica reservoir, a process that enhances redistribution of both Si and Al through the exsolving ternary feldspar. 相似文献
11.
Thermodynamic analysis of Fe and Mg partitioning between plagioclase and silicate liquid 总被引：4，自引：0，他引：4
Toru Sugawara 《Contributions to Mineralogy and Petrology》2000,138(2):101-113
Thermodynamic analysis of Fe- and Mg-bearing plagioclase and silicate liquid was carried out based on reported element partitioning
data between plagioclase and silicate liquid in reduced conditions, solution properties of ternary feldspar, standard state
properties of plagioclase endmembers and solution properties of multicomponent silicate liquid. Derived mixing properties
of Fe- and Mg-bearing plagioclase are in harmony with estimated results from synthetic experiments in the systems CaAl2Si2O8-CaFeSi3O8 and CaAl2Si2O8-CaMgSi3O8. Based on the determined solution properties of the plagioclase, a computer program to calculate the element partition relationships
between Fe- and Mg-bearing plagioclase and multicomponent silicate liquid was developed. The FeO, MgO and MgO/(MgO + FeO)
in plagioclase predicted from known liquid compositions and pressure are in agreement with measurements within 0.2 wt%, 0.1 wt%
and 0.1 (mol ratio), respectively. The Fe3+ content in plagioclase crystallized at high oxygen fugacity can be estimated with this program. The Fe3+/total Fe ratio in plagioclase crystallized near the quartz-fayalite-magnetite buffer ranges from 0 to 0.5, which is consistent
with previous study on natural plagioclase in submarine basalt. Derived solution properties of the Fe- and Mg-bearing plagioclase
are also used to calculate equilibrium composition relationship between olivine and plagioclase. Change of X
Fo in olivine coexisting with plagioclase affects MgO and FeO contents in plagioclase greatly. The present model predicts X
Fo of coexisting olivine from the chemical composition of plagioclase to ±0.1 accuracy at given pressure and temperature.
Received: 27 March 1998 / Accepted: 30 September 1999 相似文献
12.
Ferric iron contents of coexisting ortho- and clinopyroxene from spinel lherzolite xenoliths were measured with Mössbauer spectroscopy and found to be significant. In orthopyroxene, the range in Fe3+/Fe is from 0.04 to 0.14; in clinopyroxene, the range is from 0.12 to 0.24. Reactions involving coexisting olivine, orthopyroxene, and clinopyroxene, where either the esseneite (CaFe3+ AlSiO6) or the acmite (NaFe3+Si2O6) component in the clinopyroxene is considered, are used to calculate oxygen fugacities. These oxygen fugacities agree well with those calculated with the olivine-orthopyroxene-spinel oxybarometer. Because these reactions do not involve garnet, spinel, or plagioclase, they may be applied to lherzolites to give internally-consistent oxygen fugacities across the pressure-dependent facies boundaries between plagioclase, spinel, and garnet lherzolite. Another application of this method is to predict the Fe3+/Fe in clinopyroxene coexisting with olivine and orthopyroxene given pressure, temperature,
, and the compositions of the coexisting phases in either experimental or natural assemblages. At values of
equal to those of the synthetic fayalite-magnetite-quartz buffer, for example, 15–35% of the iron in the clinopyroxenes from these xenoliths would be ferric. The simplifying assumption that all Fe is divalent in silicate phases at geologically — reasonable oxygen fugacities must be re-evaluated. 相似文献
13.
The Blosseville Coast basalts of East Greenland: Their occurrence,composition and temporal variations 总被引：1，自引：0，他引：1
C. K. Brooks T. F. D. Nielsen T. S. Petersen 《Contributions to Mineralogy and Petrology》1976,58(3):279-292
In the system CaO-MgO-A12O3-SiO2 the tie lines connecting anorthite with other phases are sequentially broken down with increasing pressure according to the following univariant reactions: anorthite+ enstatitess+sillimanite pyrope-grossularss+quartz (3), anorthite+enstatitess pyrope-grossularss+diopsidess+quartz (2), anorthite+pyrope-grossularss+ quartz diopsidess+kyanite (4) and anorthite+diopsidess grossular-pyropess +kyanite+quartz (8). At 1,200 ° C these reactions occur at 14.5± 0.5, 15.5±0.5, 19.5±0.5 and 26.4±1 kilobar and have positive slopes (dP/dT) of 1±0.5, 2.8±0.5, 13.3±0.5 and 24±2bars/°C respectively. An invariant point involving kyanite rather than sillimanite, occurs at 850 °C±25 °C and 14.5±0.5kbar at the intersection of reactions (3), (2) and (4). Reaction(4) exhibits significant curvature with an increase in dP/dT from 13.3±0.5 to 18.5± 0.5 bars/°C between 1,050° and 850° C. The pressure at which the complete grossular-pyrope join is stable with quartz is estimated at 41 ± 1 kbar at 1,200 ° C. The pressure at which garnet appears according to reaction (2) is lowered by 5 kbar for a composition with anorthite and orthopyroxene (En0.5Fs0.5). Enstatite and plagioclase (An0.5Ab0.5) first produce garnet at 2 kbar higher pressure than enstatite and pure anorthite (reaction (2)). The calcium content of garnet in various divariant assemblages is relatively insensitive to temperature but very sensitive to pressure, it is therefore a useful geobarometer. At metamorphic temperatures of 700–850 °C pressures of 8–10 kbar are required for the formation of quartz-bearing garnet granulites containing calcic plagioclase and with (Mg/Mg+Fe) bulk = 0.5. 相似文献
14.
Values of silica activity have been calculated for Bushveld rocks from an extension of the mafic layered sequence north of the town of Bethal in the south-eastern Transvaal as well as the Roossenekal area in the eastern limb of the Complex. The samples examined contain the coexisting assemblage olivine, Ca-poor pyroxene, Ca-rich pyroxene and plagioclase. This enabled silica activities to be calculated from the following reactions: (Mg, Fe)2SiO4+SiO22(Mg, Fe)SiO3, CaAl2SiO6+SiO2CaAl2Si2O8. Parallel curves of increasing silica activity with fractionation were established 0.20 log units apart. This represented a pressure of emplacement for the top of the layered zone in the Bethal area of 2.72±0.79 kbars. A value of 1.47±0.62 kbars was obtained for the Roossenekal area. These values are equivalent to 9.1±2.6 km and 4.9±2.1 km respectively, the latter figure being consistent with the minimum thickness of 4550 m of felsite and granophyre originally overlying the layered sequence and still preserved in the area west of Roossenekal. 相似文献
15.
Seck's (1971a) compositional data on coexisting feldspars in the Or-Ab-An ternary at 650° C and 1 kb were used to calculate the activity-composition relations in binary alkali feldspar and binary plagioclase. The energy constants in Guggenheim's expression for excess free energy of mixing are A
0=3920 and A
1=657 cal/mole for alkali feldspar, in excellent agreement with values obtained by Thompson and Waldbaum (1969), and 1320 and 373 cal/ mole for plagioclase. Using Orville's (1972) data from ion-exchange experiments between plagioclase and Na—Ca chloride solutions at 700° C and 2 kb, we obtained 967 cal/mole for A
0 and 715 cal/mole for A
1 in the plagioclase crystalline solution.Activity-composition relations for plagioclase are interpreted in terms of a continuous, random substitution of CaAl for NaSi across the high structural state plagioclase series. This interpretation is consistent with that obtained from a consideration of lattice parameters. 相似文献
16.
The pseudo-binary system CaMgSi2O6-KAlSi2O6, modeling the potassium-bearing clinopyroxene (KCpx) solid solution, has been studied at 7 GPa and 1,100–1,650 °C. The KCpx is a liquidus phase of the system up to 60 mol% of KAlSi2O6. At higher content of KAlSi2O6 in the system, grossular-rich garnet becomes a liquidus phase. Above 75 mol% of KAlSi2O6 in the system, KCpx is unstable at the solidus as well, and garnet coexists with kalsilite, Si-wadeite and kyanite. No coexistence of KCpx with kyanite was observed. Above the solidus, KAlSi2O6 content of the KCpx coexisting with melt increases with decreasing temperature. Near the solidus of the system (about 1,250 °C) KCpx contains up to 5.6 wt% of K2O, i.e. about 22–26 mol% of KAlSi2O6. Such high concentration of potassium in KCpx is presumably the maximal content of KAlSi2O6 in the Fe-free clinopyroxene at 7 GPa. In addition to the major substitution MgM1C2Al1K2, the KCpx solid solution contains Ca-Eskola and only minor Ca-Tschermack components. Our experimental results indicate that the natural assemblage KCpx+grossular-rich garnet might be a product of crystallization of the ultra-potassic SiO2-rich alumino-silicate mantle melts (>200 km).Editorial responsibility: J. Hoefs 相似文献
17.
R. Kerrich W. S. Fyfe R. L. Barnett B. B. Blair L. M. Willmore 《Contributions to Mineralogy and Petrology》1987,95(4):481-498
Monomineralic domains of chlorite, corundum and Cr muscovite coexist over a kilometer scale within ultramafic schists of the Harare greenstone belt (2.73 Ga). This exotic lithological association includes the conjunction of some of the most aluminous (Al2O388 wt%) and potassic (K2O10 wt%) rocks known. The paragenetic sequence developed from chloritecorundumcorundum+ diaspore: Cr muscovite variably overprinted both the corundum and chloritite domains. Terminal stages were marked by sporadic production of andalusite+quartz, and finally margarite.Chlorite (Cr2O3=0.31–2.65 wt%), corundum (0.79–2.66 wt%), and diaspore are all Cr-rich varieties. The chromian (Cr2O33.86 wt%) paragonitic muscovite incorporates up to 17% of the paragonite molecule, and significant Mg and Fe substitutions.The suite of rocks are characterized by chondritic Ti/Zr ratios (–x=107), systematically enhanced Cr (up to 14000 ppm) and Ni (up to 1200 ppm) abundances, low levels of the alteration-insensitive incompatible elements Th, Ta, Nb. Chlorite, corundum and Cr muscovite represent progressive stages in the incremental metasomatic alteration of a komatiite precursor. Mass balance calculations, constrained by the isochemical behaviour of Ti, Zr and Hf reveal that the komatiite chloritite transformation involved volumetric contractions of 60% by hydrothermal leaching of Si, Fe, Mn, Ca and Na. Reaction of chloritite to corundum involved further volumetric reductions of 50% due to essentially quantitative loss of Si, Fe, Mn, Mg, K and Ca. Conversion of corundum to muscovite required additions of Si, K, Fe, Mn, Mg, Rb and Ba at 50–200% dilation. K, Rb, Ba, Li and Cs are enriched by up to 2×103 over background abundances in ultramafic rocks, and the suite is also enriched in B, Se, Te, Bi, As, Sb and Au. REE were extensively leached during chloritite-corundum stages, whereas LREE additions accompany development of muscovite. Ti, Zr, Hf and Al were all concentrated by selective leaching of mobile components, but absolute additions of Al accompanied development of the corundum domains due to Al precipitation in response to depressurization.Corundum (
18O=3.5–4.8), muscovite (
18O=6.7–7.5) and chlorite (4.5–5.6) are isotopically uniform and formed at 380–520° C from a fluid where
18O=5.6–6.9. The corundum is 18O depleted relative to either igneous or anatectic counterparts (Ocor=7.6–8.2), or to gibbsitic laterites (
18O=12–17).Previous genetic schemes involving metamorphism of exhalites or bauxite, or Si-undersaturation of magmas, can all be ruled out from the data. The chloritite, corundum, Cr-muscovite association represents sequential alteration products of ultramafic rocks by high temperature, low pH hydrothermal solutions carrying LIL-elements, and in which excursions of pH and/or degree of quartz undersaturation account for the mineralogical transitions. A deep level acid epithermal system, or fluid advection across steep inverted thermal gradients in a thrust regime could account for required hydrothermal conditions. 相似文献
18.
Amphibole-plagioclase equilibria: An empirical model for the relation albite+tremolite=edenite+4 quartz 总被引：2，自引：0，他引：2
Frank S. Spear 《Contributions to Mineralogy and Petrology》1981,77(4):355-364
Equilibria between plagioclase, calcic amphibole and quartz can be described, in part, by the relation among mineral components: NaAlSi3O8+Ca2Mg5Si8O22(OH)2 = NaCa2Mg5AlSi7O22(OH)2+4SiO2; this relation governs the partitioning of Na between plagioclase and the A-site of coexisting amphibole. Data from natural amphibolites reveal that this partitioning is systematic and sensitive to metamorphic grade. The ideal portion of the equilibrium constant (K
id = X
Na, A/X, A · X
Ab) derived from natural samples is sensitive to bulk composition, inasmuch as both plagioclase and amphibole are highly non-ideal. Samples from a single outcrop have values ranging from 0.5 (X
Ab=0.74) to 4.1 (X
Ab=0.10). The continuous reaction, NaAlSi3O8+Ca2Mg5Si8O22(OH)2 = NaCa2Mg5AlSi7O22(OH)2+4SiO2, proceeds to the right with increasing grade of metamorphism and for a given bulk composition, K
id increases with increasing temperature. Two related discontinuous reactions, actinolite+albite=hornblende+oligoclase+quartz and actinolite+oligoclase=hornblende+anorthite+quartz, also proceed to the right with increasing metamorphic grade and result in changes in the topology of a phase diagram that describes the partitioning of Na between plagioclase and amphibole A-site. A Schreinemakers' net is presented that is consistent with natural occurrences. The results of this study should aid in the delineation of metamorphic facies within amphibolites. 相似文献
19.
Iron- and vanadium-bearing kyanites have been synthesized at 900 and 1100° C/20 kb in a piston-cylinder apparatus using Mn2O3/Mn3O4- and MnO/Mn-mixtures, respectively, as oxygen buffers. Solid solubility on the pseudobinary section Al2SiO5-Fe2SiO5(-V2SiO5) of the system Al2O3-Fe2O3(V2O3)-SiO2 extends up to 6.5 mole% (14mole %) of the theoretical end member FeSiO5(V2SiO5) at 900°C/20 kb. For bulk compositions with higher Fe2SiO5 (V2SiO5) contents the corundum type phases M2O3(M = Fe3+, V3+) are found to coexist with the Fe3+(V3+)-saturated kyanite solid solution plus quartz. The extent of solid solubility on the join Al2SiO5-Fe2SiO5 at 1 100°C was not found to be significantly higher than at 900° C. Microprobe analyses of iron bearing kyanites gave no significant indication of ternary solid solubility in these mixed crystals. Lattice constants a
0, b
0, c
0, and V0 of the kyanite solid solutions increase with increasing Fe2SiO5- and V2SiO5-contents proportionally to the ionic radii of Fe3+ and V3+, respectively, the triclinic angles ,, remain constant. Iron kyanites are light yellowish-green, vanadium kyanites are light green. Iron kyanites, (Al1.87 Fe
0.13
3+
)SiO5, were obtained as crystals up to 700 m in length. 相似文献
20.
Coexisting feldspars from across 2,000 km2 of the granulite facies Oaxacan Complex, southern Mexico exhibit variable amounts of solid solution from nearly binary (Ab-An and Ab-Or) to substantially ternary (Ab-An-Or). Reintegrated analyses of 21 coarsely exsolved perthite (AF)-plagioclase (PL) pairs yield AF=Or30–63 Ab30–56An2–15 and PL=Or1–2Ab70–84An11–28. These data have been used to test existing two feldspar geothermometers for this extended composition range.For all compositions, temperature estimates show relatively little spread in value (660° to 795° C, 7 kbar) using the Haselton et al. (1983) calibration (HHHR). These temperatures are in fair agreement with estimates of 750±40° C for feldspar pairs with nearly binary compositions using the Stormer (1975) thermometer (STO). However, STO temperatures increase significantly (to 990° C) with increasing ternary solid solution in AF, suggesting that thermometers derived for binary systems are inaccurate for ternary compositions. Isotherms drawn from HHHR which take into account variable anorthite solution in alkali feldspar show that estimated temperature decreased by 50–100° C for each 5 mole percent anorthite in alkali feldspar.Experimentally determined solvus relations (Seck 1971) require feldspars with significant ternary solid solution to have crystallized or to have equilibrated at higher temperature than feldspars with more binary compositions. However, petrographic and field relations of ternary and binary feldspars in the Oaxacan Complex suggest they were all equilibrated at similar metamorphic pressures and temperatures and do not support a model where ternary feldspars have preserved higher premetamorphic temperatures. The composition of coexisting feldspars from other Precambrian granulite-facies terranes are also inconsistent with Seck's (1971) results. Hence, thermometers which fit Seck's solvus relations may not yield accurate temperatures in high grade metamorphic terranes. Parallel tie-lines for ternary and binary feldspars in the Oaxacan Complex and the consistency of inferred temperatures (HHHR) for many granulite terranes suggest that estimation of temperature using tie-line slopes rather than solvus width may yield more accurate results for these samples.Peak metamorphic conditions in the Oaxacan Complex are inferred to have been 730±50° C, 7±1 kbar. Pressure estimates from four garnet-plagioclase barometers show good agreement. Results of feldspar thermometry are consistent with diopside-forsterite equilibria in marbles which restrict T=720–765° C at P=7 kbar. 相似文献