一种斜长石地质温度计的改进

鲍温(N. L. Bowen)在他的关于斜长石熔融特性的经典论述中曾证明,钠长石(NaAlSi₃O₈)和钙长石(CaAl₂Si₂O₈)在高温下形成一个连续的固溶体系列,他按照理想溶液的模式对其试验资料进行了解释。许多年来,岩石、矿物学工作者一直试图以鲍温1913年的斜长石系统的实验研究为基础,找出岩浆岩中斜长石结晶温度与平衡共存的斜长石晶体和液体成分间的关系。库多和韦尔(A.M. Kudo和D.F. Weill)首次获得成功,他们于1970年,主要根据花岗岩和钠长石-钙长石二元系的实验资料,用一种经验的方法建立起一个地质温度计,目前已被通称为Kudo-weill斜长石地质温度计。     

A regular solution model for met-aluminous silicate liquids: Applications to geothermometry,immiscibility, and the source regions of basic magmas

Adopting a set of multioxide components and using published compositional data on olivineand plagioclase-liquid equilibria we have developed a 17 component regular solution model for met-aluminous silicate liquids. The partial molar excess free energies predicted from this model can be used together with phenocryst compositions as an effective geothermometer, with an approximate error of 20 °C (30 °C for olivine, 12 °C for plagioclase). The regular solution formulation is also successful in predicting liquid immiscibility at (1) high mole fractions of silica commonly observed in phase diagrams, and at (2) lower temperatures in lunar basalts and intermediate lavas. The model yields activities of silica which are consistent with those obtained from solid-liquid silica buffers in rocks which contain olivine and enstatite or quartz. From predicted activities of KAlSi₃O₈ in liquids coexisting with plagioclase a value is obtained for the limiting Henry's law activity coefficient of KAlSi₃O₈ in the solid. This coefficient agrees well with that inferred from plagioclase-sanidine equilibrium phenocryst assemblages in rhyolites. The activities of silica obtained from this model are used to place constraints on the pressure-temperature regions where various types of basic magmas are generated. In conjunction with plagioclase geothermometry an application is given where the pressure, temperature, and water content of an olivine andesite is predicted from the activity of silica.     

The Kudo-Weill plagioclase geothermometer and porphyritic acid glasses

The compositions of the cores and margins of the plagioclase phenocrysts in glassy acid rocks have been used to derive equilibration temperatures with their enclosing liquids using the Kudo-Weill geothermometer. The equilibration temperatures inferred from the compositions of the feldspar margins at 0.5 kilobars water pressure, or less, agree well with the temperatures obtained from the coexisting iron-titanium oxide microphenocrysts. These low water pressures are supported by the water fugacities deduced from the coexisting biotitemagnetite-sanidine assemblages. Acid magma represented by these rocks has a crystallization interval in excess of 100° C and liquidus temperatures above 900° C.     

An empirical model for plagioclase equilibrium in hydrous melts

Heat capacity models for anorthite (An) and albite (Ab) crystal and supercooled liquid, together with the assumption of ideal mixing of these components were used to derive average values of enthalpy and volume of melting from phase equilibrium data that are in significant disagreement with some recently published thermodynamic data. In an effort to find a means of calculating both liquidus temperature and crystal composition of plagioclase for a given hydrous melt composition, the activity models for feldspar components in hydrous melts and solubility calculations suggested by Burnham (1975) and the enthalpy data above were tested by comparing predicted and observed liquidi. These assumptions lead to satisfactory agreement in the systems Ab-An-H₂O and Ab-Si₄O₈-H₂O but liquidi in the system An-Si₄O₈-H₂O and complex systems differ radically from those calculated. For hydrous complex melts an empirical model using the above solubility and activity assumptions was fit to experimental data on coexisting melt and plagioclase compositions. Despite the demonstrable theoretical limitations of the assumptions involved, this empirical model apparently balances inaccuracies and reproduces the original data with absolute mean errors for 66 experiments of 17°C and 5 mol% An. It is sufficiently precise for use in kinetic crystallization models and may be useful as a geothermometer in some applications; it is probably not sufficiently accurate to be used as a geobarometer.     

Ancient conglomerates of the Kursk Magnetic Anomaly

Two of the most well-preserved igneous bodies in the early Preeambrian White Sea complex— the Severnyy and Yuzhnyy massifs on Pezhostrov Island—have been studied in order to gain a better understanding of ultramafic-mafic magmatism in the Belomorian tectonic block. These massifs represent portions of a single, differentiated pluton, ranging in composition from lherzolite to gabbronorite to anorthosite.

Mineral-chemical and trace-element compositions of chill margins from this pluton were used to model the differentiation in this ancient magma chamber. Major-element compositions of minerals suggest that plagioclase in these rocks is not in equilibrium with the mafic minerals. This possibly is the result of suspension of less dense, early-formed plagioclase in more dense, early residual liquids. Later, as the liquid density decreased because of precipitation of mafic phases, plagioclase began to precipitate. We speculate that the liquid density did not decrease to a point where plagioclase would settle, until after 15 to 30% crystallization of the parent magma. However, this early-formed plagioclase would not have been in chemical equilibrium with the later-forming mafic silicates. Toward the end of crystallization in the chamber, plagioclase precipitated in equilibrium with the mafic minerals. Trace-element modeling indicates that the rocks that form the pluton originally were precipitated as liquid-dominated cumulates.

The trace-element and mineral-chemical compositions of the parent liquid (s) of the Pezhostrov pluton were enriched in the LILE (Sr, Rb, Ba, La) and depleted in the HFSE (Zr, Ti, Y) relative to present-day MORB. These magmas are suggested to be roughly boninitic in composition, and are similar to those parental to other mafic plutons of similar age worldwide, including the Stillwater intrusion, Montana, USA. Thus, this character of magmatism may represent an important episode of mantle melting worldwide during the late Archean and early Proterozoic.     

A REE-in-plagioclase–clinopyroxene thermometer for crustal rocks

A REE-in-plagioclase-clinopyroxene thermometer has been developed on the basis of the temperature- and composition-dependent rare-earth element (REE) partitioning between coexisting plagioclase and clinopyroxene. This two-mineral exchange thermobarometer is constructed using parameters from lattice strain models for REE?+?Y partitioning in plagioclase and in clinopyroxene that were independently calibrated against experimentally determined mineral-melt partitioning data. An important advantage of this REE-based thermometer is that it can provide accurate temperatures through linear least-squares analysis of REE?+?Y as a group. Applications of the REE-in-plagioclase-clinopyroxene thermometer to volcanic and cumulate rocks show that temperatures derived from the new thermometer agree well with independently constrained magma crystallization temperatures, which adds confidence to applications of the REE-exchange thermometer to natural rocks with a wide spectrum of composition (i.e., from basalt to rhyolite). However, systematic temperature differences appear between the REE- and Mg-exchange thermometers for the volcanic and cumulate rocks. Through numerical simulations of diffusion in plagioclase-clinopyroxene systems, we demonstrate that (1) due to their slower diffusion rates, REE in minerals preferentially records crystallization or near-crystallization temperatures of the rock, and that (2) Mg is readily rest to lower temperatures for rocks from intermediately or slowly cooled magma bodies but records the initial crystallization temperatures of rocks from rapidly cooled magmas. Given their distinct diffusive responses to temperature changes, REE and Mg closure temperatures recorded by the two thermometers can be used in concert to study thermal and magmatic histories of plagioclase- and clinopyroxene-bearing rocks.     

Thermodynamic analysis of Fe and Mg partitioning between plagioclase and silicate liquid

 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     

Multiphase inclusions in plagioclase from anorthosites in the Stillwater Complex,Montana: implications for the origin of the anorthosites

Multiphase inclusions, consisting of clinopyroxene+ilmenite+apatite, occur within cumulus plagioclase grains from anorthosites in the Stillwater Complex, Montana, and in other rocks from the Middle Banded series of the intrusion. The textures and constant modal mineralogy of the inclusions indicate that they were incorporated in the plagioclase as liquid droplets that later crystallized rather than as solid aggregates. Their unusual assemblage, including a distinctive manganiferous ilmenite and the presence of baddeleyite (ZrO₂), indicates formation from an unusual liquid. A process involving silicater liquid immiscibility is proposed, whereby small globules of a liquid enriched in Mg, Fe, Ca, Ti, P, REE, Zr and Mn exsolved from the main liquid that gave rise to the anorthosites, became trapped in the plagioclase, and later crystallized to form the inclusions. The immiscibility could have occurred locally within compositional boundaries around crystallizing plagioclase grains or it could have occurred pervasively throughout the liquid. It is proposed that the two immiscible liquids were analogous, n terms of their melt structures, to immiscible liquid pairs reported in the literature both in experiments and in natural basalts. For the previously reported pairs, immiscibility is between a highly polymerized liquid, typically granitic in composition, and a depolymerized liquid, typically ferrobasaltic in composition. In the case of the anorthosites, the depolymerized liquid is represented by the inclusions, and the other liquid was a highly polymerized aluminosilicate melt with a high normative plagioclase content from which the bulk of the anorthosites crystallized. Crystallization of the anorthosites from this highly polymerized liquid accounts for various distinctive textural and chemical features of the anorthosites compared to other rocks in the Stillwater Complex. A lack of correlation between P contents and chondrite-normalized rare earth element (REE) ratios of plagioclase separates indicates that the amount of apatite in the inclusions is too low to affect the REE signature of the plagioclase separates. Nevertheless, workers should use caution when attempting REE modelling studies of cumulates having low REE contents, because apatite-bearing inclusions can potentially cause problems.     

Distribution of elements in coexisting minerals and the problem of chemical disequilibrium in metamorphosed basic rocks

Distribution of elements in coexisting minerals—biotite, hornblende, augite, hypersthene and plagioclase in charnockitic rocks of West Uusimaa Complex, Finland, is mostly orderly indicating a close approach to chemical equilibrium. The distribution of iron and magnesium in coexisting hornblende and pyroxenes of basic charnockites and other rocks of granulite facies from several different areas is also orderly but the variation in the fugacities of H₂O and H₂ may cause a disorderly distribution locally in some rocks. The probable oxidation or reduction reactions are discussed on the basis of thermochemical and mineralchemical data.     

The role of H2O during crystallization of primitive arc magmas under uppermost mantle conditions and genesis of igneous pyroxenites: an experimental study

Exposed, subduction-related magmatic arcs commonly include sections of ultramafic plutonic rocks that are composed of dunite, wehrlite, and pyroxenite. In this experimental study we examined the effects of variable H₂O concentration on the phase proportions and compositions of igneous pyroxenites and related ultramafic plutonic rocks. Igneous crystallization experiments simulated natural, arc magma compositions at 1.2 GPa, corresponding to conditions of the arc lower crust. Increasing H₂O concentration in the liquid changes the crystallization sequence. Low H₂O concentration in the liquid stabilizes plagioclase earlier than garnet and amphibole while derivative liquids remain quartz normative. Higher H₂O contents (>3%) suppress plagioclase and lead to crystallization of amphibole and garnet thereby producing derivative corundum normative andesite liquids. The experiments show that alumina in the liquid correlates positively with Al in pyroxene, as long as no major aluminous phase crystallizes. Extrapolation of this correlation to natural pyroxenites in the Talkeetna and Kohistan arc sections indicates that clinopyroxenes with low Ca-Tschermaks component represent near-liquidus phases of primitive, Si-rich hydrous magmas. Density calculations on the residual solid assemblages indicate that ultramafic plutonic rocks are always denser than upper mantle rocks in the order of 0.05 to 0.20 g/cm³. The combination of high pressure and high H₂O concentration in the liquid suppresses plagioclase crystallization, so that ultramafic plutonic rocks form over a significant proportion of the crystallization interval (up to 50% crystallization of ultramafic rocks from initial, mantle-derived liquids). This suggests that in subduction-related magmatic arcs the seismic Moho might be shallower than the petrologic crust/mantle transition. It is therefore possible that calculations based on seismic data have overestimated the normative plagioclase content (e.g., SiO₂, Al₂O₃) of igneous crust in arcs.     

Possible role of amphibole in the origin of andesite: some experimental and natural evidence

Experiments in the system high-A1 basalt (HAB)-water have been conducted in the melting range at pressures between 1 atm. and 10 kbar, defining the amphibole stability field and the composition of liquids which coexist with this amphibole. Plagioclase is the anhydrous liquidus phase between 1 atm. and 10 kbar but in the hydrous runs this role is taken by olivine at <7 kbar and then by clinopyroxene at higher pressures. Because amphibole is never on the high-A1 basalt liquidus it is not likely that andesite is derived from primary basalt by pure fractional crystallisation, although as we discuss, other mechanisms including equilibrium crystallisation might implicate amphibole. If primary basaltic magma undergoes closed-system equilibrium crystallisation, then the amphibole field will be intersected at between 50 and 100°C below the liquidus. The compositions of melts coexisting with amphibole alone do not match those of any of the natural andesite or dacitic lavas associated with the particular high-A1 basalt investigated. Like natural andesites, they become rapidly silica enriched, but they also become far more depleted in TiO₂ and MgO. However, the compositions of liquids lying directly on the divariant amphibole-out reaction zone, where amphibole +liquid coexist with clinopyroxene or olivine (±plagioclase), do resemble those of naturally occurring low-silica andesites. With increasing temperature pargasitic amphibole breaks down via incongruent melting reactions over a narrow temperature range to form a large volume of relatively low-silica basaltic andesite liquid and a crystalline assemblage dominated by either clinopyroxene or olivine. Our important conclusion is that basaltic andesite liquid will be the product of reaction between cooling, hydrous mafic liquid and anhydrous ferromagnesian phases. The solid reactants could represent earlier cumulates from the same or different magma batches, or they could be peridotite wall-rock material. Because the amphibole-out boundary coexisting with liquid is one of reaction, it will not be traversed so long as the phases on the high temperature side remain. Thus, the assemblage amphibole+clinopyroxene±olivine±plagioclase+liquid is one in which the liquid is buffered (within limits), and results reported here indicate that this buffering generates melts of low-silica andesite composition. When tapped to lower pressures these liquids will rise, eventually to fractionate plagioclase-rich assemblages yielding silicarich andesite and dacite melts. Conversely, the partial melting of hornblende pyroxenite, hornblende peridotite or hornblende gabbro can also yield basaltic andesite liquids. The phase relationships suggested by these experiments are discussed in the light of naturally occurring phenocryst and xenolith assemblages from the east Sunda Arc. Primary magmatic additions to the lithosphere of volcanic arcs are basaltic and voluminous upper crustal andesite in these terranes, complemented by mafic and ultramafic crystalline deposits emplaced in the lower crust or close to the Moho. Together these components constitute total arc growth with a basaltic composition and represent the net accreted contribution to continental growth.     

Two-feldspar geothermometry in granulite facies metamorphic rocks

A geothermometric technique based on equilibria between coexisting plagioclase and alkali feldspar was applied to quartzo-feldspathic granulites from Salvador, BA, Brazil. The conditions of metamorphism were determined to be in the range 750 ° C–800 ° C, 4–8 Kb, by comparison with experimental data on the stabilities of sapphirine, phlogopite and other minerals occurring in the associated rocks. Selected feldspar data gives temperatures near, but slightly below, this range. Several variants of the Wood and Banno model, as well as an empirical two-pyroxene geothermometer, were also tested and found to give temperatures which were apparently 50 °–100 ° high. The solubility of Al₂O₃ in orthopyroxene indicates temperatures which are about 200 ° to high, suggesting that Fe in the natural assemblages significantly changes relationships observed experimentally in MgO-Al₂O₃-SiO₂ systems.     

Age and Thermal History of the East Ore Section,Bayan,Obo Deposit—A Fission Track Study

Considerable attention has been paid in recent years to the study of geothermal history by using spontaneous fission tracks of 238U recorded in minerals.Apatite and zircon were used for fission track study in this paper because apatitie has been widely used as a natural geothermometer(Wang Shicheng et al., 1994) to reveal the thermal evolution of sedimentary rocks based on its low annealing temperature of fission tracks and zircon is characterized by a closing temperature above 700℃,The samples were collected from ferruginous,siliceous slate wall rock at the upper levels of the orebody and Nb-REE-Fe ores from deep tunnels.The age and thermal evolution of the orebody were discussed in terms of fission track characters and their length variations observed in the coexisting apatite and zircon in the same specimen.     

Spinel-olivine geothermometry in peridotites from ultramafic complexes

An empirical calibration of the spinel-olivine geothermometer (Evans and Frost, 1975) is attempted and applied to parageneses of lherzolitic rocks. In ultramafic complexes, most of the derived temperature estimates range between 700 ° and 850 °C, and appear generally lower than those given by other geothermometers, based upon Ca or Al contents of coexisting pyroxenes. A comparison of the different thermometric data in two well studied occurrences, the Ronda ultramafic complex and the San Carlos xenolith field, suggests that differential rates of diffusion and recrystalization may account for the large range of temperatures (between 700 ° and 1200 °C) determined by various mineral geothermometers in peridotites. The equilibrium exchange of Mg and Fe between spinel and olivine would be the fastest one and would continue effectively during the cooling down to relatively low temperatures, while other exchange reactions used as geothermometers in peridotites, like partitioning of Ca and Al in coexisting pyroxenes, are blocked at higher temperatures.     

Melting and phase relations in the plane tholeiite-lherzolite-nepheline basanite to 40 kilobars with geological implications

Six crystalline mixtures, picrite, olivine-rich tholeiite, nepheline basanite, alkali picrite, olivine-rich basanite, and olivine-rich alkali basalt were recrystallized at pressures to 40 kb, and the phase equilibria and sequences of phases in natural basaltic and peridotitic rocks were investigated.The picrite was recrystallized along the solidus to the assemblages (1) olivine+orthopyroxene+ clinopyroxene +plagioclase+spinel below 13 kb, (2) olivine+orthopyroxene+clinopyroxene+spinel between 13 kb and 18 kb, (3) olivine+orthopyroxene+clinopyroxene+ garnet+spinel between 18 kb and 26 kb, and (4) olivine+clinopyroxene+garnet above 26 kb. The solidus temperature at 1 atm is slightly below 1,100° and rises to 1,320° at 20 kb and 1,570° at 40 kb. Olivine is the primary phase crystallizing from the melt at all pressures to 40 kb.The olivine-rich tholeiite was recrystallized along the solidus into the assemblages (1) olivine+ clinopyroxene+plagioclase+spinel below 13 kb, (2) clinopyroxene+orthopyroxene+ spinel between 13 kb and 18 kb, (3) clinopyroxene+garnet+spinel above 18 kb. The solidus temperature is slightly below 1,100° at 1 atm, 1,370° at 20 kb, and 1,590° at 40 kb. The primary phase is olivine below 20 kb but is orthopyroxene at 40 kb.In the nepheline basanite, olivine is the primary phase below 14 kb, but clinopyroxene is the first phase to appear above 14 kb. In the alkali-picrite the primary phase is olivine to 40 kb. In the olivine-rich basanite, olivine is the primary phase below 35 kb and garnet is the primary phase above 35 kb. In the olivine-rich alkali basalt the primary phase is olivine below 20 kb and is garnet at 40 kb.Mineral assemblages in a granite-basalt-peridotite join are summarized according to reported experimental data on natural rocks. The solidus of mafic rock is approximately given by T=12.5 P _Kb+1,050°. With increasing pressure along the solidus, olivine disappears by reaction with plagioclase at 9 kb in mafic rocks and plagioclase disappears by reaction with olivine at 13 kb in ultramafic rocks. Plagioclase disappears at around 22 kb in mafic rocks, but it persists to higher pressure in acidic rocks. Garnet appears at somewhat above 18 kb in acidic rocks, at 17 kb in mafic rocks, and at 22 kb in ultramafic rocks.The subsolidus equilibrium curves of the reactions are extrapolated according to equilibrium curves of related reactions in simple systems. The pyroxene-hornfels and sanidinite facies is the lowest pressure mineral facies. The pyroxene-granulite facies is an intermediate low pressure mineral facies in which olivine and plagioclase are incompatible and garnet is absent in mafic rocks. The low pressure boundary is at 7.5 kb at 750° C and at 9.5 kb at 1,150° C. The high pressure boundary is 8.0 kb at 750° C and 15.0 kb at 1,150° C. The garnet-granulite facies is an intermediate high pressure facies and is characterized by coexisting garnet and plagioclase in mafic rocks. The upper boundary is at 10.3 kb at 750° C and 18.0 kb at 1,150° C. The eclogite facies is the highest pressure mineral facies, in which jadeite-rich clinopyroxene is stable.Compositions of minerals in natural rocks of the granulite facies and the eclogite facies are considered. Clinopyroxenes in the granulite-facies rocks have smaller jadeite-Tschermak's molecule ratios and higher amounts of Tschermak's molecule than clinopyroxenes in the eclogite-facies rocks. The distribution coefficients of Mg between orthopyroxene and clinopyroxene are normally in the range of 0.5–0.6 in metamorphic rocks in the granulite facies. The distribution coefficients of Mg between garnet and clinopyroxene suggest increasing crystallization temperature of the rocks in the following order: eclogite in glaucophane schist, eclogite and granulite in gneissic terrain, garnet peridotite, and peridotite nodules in kimberlite.Temperatures near the bottom of the crust in orogenic zones characterized by kyanitesillimanite metamorpbism are estimated from the mineral assemblages of metamorphic rocks in Precambrian shields to be about 700° C at 7 kb and 800° C at 9 kb, although heat-flow data suggest that the bottom of Precambrian shield areas is about 400° C and the eclogite facies is stable.The composition of liquid which is in equilibrium with peridotite is estimated to be close to tholeiite basalt at the surface pressure and to be picrite at around 30 kb. The liquid composition becomes poorer in normative olivine with decreasing pressure and temperature.During crystallization at high pressure, olivine and orthopyroxene react with liquid to form clinopyroxene, and a discontinuous reaction series, olivine orthopyroxene clinopyroxene is suggested. By fractional crystallization of pyroxenes the liquid will become poorer in SiO₂. Therefore, if liquid formed by partial melting of peridotite in the mantle slowly rises maintaining equilibrium with the surrounding peridotite, the liquid will become poorer in MgO by crystallization of olivine, and tholeiite basalt magma will arrive at the surface. On the other hand, if the liquid undergoes fractional crystallization in the mantle, the liquid may change in composition to alkali-basalt magma and alkali-basalt volcanism may be seen at a late stage of volcanic activity.Publication No. 681, Institute of Geophysics and Planetary Physics, University of California, Los Angeles.     

Compatible P-T conditions for eclogites and surrounding gneisses in the Kristiansund area,western Norway

Analyses of coexisting garnets, clinopyroxenes and plagioclases from eclogites and high pressure granulitic gneisses in the Kristiansund area within the west Norwegian basal gneiss region are used to establish the P-T conditions for the metamorphic peak for these rocks. Based on the distribution of Fe and Mg between coexisting garnet and clinopyroxene in both eclogite and granulites, equilibrium temperatures are estimated to 750 °±50 ° C. Pressures are derived from the absence of orthopyroxenes in the granulites, and from the assemblage clinopyroxene +plagioclase+quartz present in the gneisses. Equilibrium pressures are estimated to 18.5±3.0 kilobars, and these equilibrium conditions are thus compatible with equilibrium conditions derived for both orthopyroxene-free and most orthopyroxene-bearing country-rock eclogites from adjacent areas.     

Calibration of the garnet–biotite–Al2SiO5–quartz geobarometer for metapelites

A garnet–biotite–Al₂SiO₅–quartz (GBAQ) geobarometer was empirically calibrated using more than 700 natural metapelites with a broad compositional range of garnet and biotite under P–T conditions of 450–950°C and 1–17 kbar. In the calibration, activity models of garnet and biotite identical to those in the garnet–biotite (GB) geothermometer of Holdaway [American Mineralogist 2000, 85: 881–892] were used. Therefore, the GBAQ geobarometer and the GB geothermometer can be simultaneously applied to iteratively estimate metamorphic P–T conditions. Successful applications of the GBAQ geobarometer to natural metapelites certify its validity. Most importantly, when plagioclase is absent or CaO components in garnet and/or plagioclase are deficient, this geobarometer may prove useful for estimating metamorphic pressures. The random error of the present GBAQ geobarometer is inferred to be around ±1.8 kbar. An electronic spreadsheet is available as Table S4 to apply the GBAQ geobarometer in combination with the GB geothermometer.     

高温变泥质岩石中石榴石-黑云母地质温度计的应用——以胶北荆山群富铝岩石为例

在对胶北荆山群麻粒岩相富铝岩石中石榴石、黑云母的成分环带进行深入研究基础上,选取不同粒径、与不同矿物相邻的石榴石、黑云母各微区点成分,利用石榴石-黑云母温度计分别进行了温度估算。确定在黑云母含量较高的岩石(V_(Grt)/V_(Bt)≤1)中,利用大颗粒石榴石(d≥1500μm)晶体核部(或靠近长英质矿物一侧的晶体幔部)成分与基质中远离石榴石等镁铁矿物处于长英质矿物之间的黑云母核部成分配合。通过石榴石-黑云母温度计可以获得相当可信的变质峰期温度。但是对于黑云母含量极低的岩石(V_(Grt)/V_(Bt)≥6),由于黑云母的成分普遍遭到了强烈改造。使得温度估算结果异常偏低,因此不适合采用石榴石-黑云母温度计估算峰期温度。同一岩石中,采用不同的相邻石榴石-黑云母矿物对晶体边缘成分获得的温度值差异较大,反映它们在峰期后发生Fe-Mg交换反应并达到封闭温度平衡状态的程度不同,因此利用石榴石-黑云母温度计难以获得准确的封闭温度。通过热力学计算,建立了一个新的石榴石-黑云母温度计公式。确定胶北荆山群所经历的变质峰期温度为720～770℃,峰期后最低相对封闭温度为480～500℃。     

Temperature and pressure dependence of Fe-Mg partitioning between garnet and phengite,with particular reference to eclogites

Experimental data combined with data from natural rocks have been used to calibrate a geothermometer based on the distribution of Fe²⁺ and Mg between coexisting garnets and phengites. The pressure effect on the K _D -value appears to be considerable. The calculated thermometer is expressed as $$T(K) = \frac{{3685 + 77.1P(kb)}}{{InK_D + 3.52}}.$$ The use of this \(K_{D_{(FeO/MgO)} }^{ga + ph}\) geothermometer on eclogites with low Fe₂O₃ content, gives P-T values which are in good accordance with those obtained by other methods. The problems that arise when Fe³⁺ is present in larger amounts, are discussed.     

Peralkaline silicic melts of island arcs, active continental margins, and intraplate continental settings: Evidence from the investigation of melt inclusions in minerals and quenched glasses of rocks

Based on the analysis of data on the composition of melt inclusions in minerals and quenched glasses of igneous rocks, we considered the problems of the formation of peralkaline silicic magmas (i.e., whose agpaitic index, the molar ratio AI = (Na₂O + K₂O)/Al₂O₃, is higher than one). The mean compositions of peralkaline silicic melts are reported for island arcs and active continental margins and compared with the compositions of melts from other settings, primarily, intraplate continental areas. Peralkaline silicic rocks are rather common in the latter. Such rocks are rare in island arcs and active continental margins, but agpaitic melts were observed in inclusions in phenocrysts of plagioclase, quartz, pyroxene, and other minerals. Plagioclase fractionation from an alkali-rich melt with AI < 1 is considered as a possible mechanism for the formation of peralkaline silicic melts (Bowen’s plagioclase effect). However, the analysis of available experimental data on plagioclase-melt equilibria showed that natural peralkaline melts are almost never in equilibrium with plagioclase. For the same reason, the melting of the majority of crustal rocks, which usually contain plagioclase, does not produce peralkaline melts. The existence of peralkaline silicic melt inclusions in plagioclase phenocrysts suggests that plagioclase can crystallize from peralkaline melts, and the plagioclase effect may play a certain role. Another mechanism for the formation of peralkaline silicic magmas is the melting of alkali-rich basic and intermediate rocks, including the spilitized varieties of subalkali basalts.