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1.
Rock Maker is a simple software tool that computes bulk rock compositions resulting from mixing or unmixing of rocks or minerals. The calculations describe the chemical expression of processes such as magma mixing, fractional crystallization, assimilation, residual melt extraction, or formation of solid solutions. Rock Maker can also be used for the elimination of thermodynamically inactive or unwanted chemical components from the whole rock composition, such as cores of porphyroblasts that are considered not to be in equilibrium with the matrix. The calculation of the resulting rock composition is essentially based on modal proportions and compositions of different components in rocks, which may include specific portions of the rock or individual mineral phases. Compositional data, obtained using XRF, ICPMS, EDS, or EPMA, may include major and trace element concentrations. Depending upon the nature of the problem to be solved, the concentrations of oxidic and elemental components can be added to, or subtracted from, each other, producing the calculated normalized whole rock composition after completion of the investigated process (mixing, unmixing, depletion, enrichment, etc.). Furthermore, the software allows the calculation of whole rock compositions from ideal mineral compositions, for which modal proportions can be chosen from pre-defined mineral compositions. The data set includes the most common rock forming minerals and allows the addition of further phases. This section can be used to calculate the approximate whole rock compositions from petrographic modal analysis. This part of Rock Maker is specifically suitable as a teaching tool that illustrates the interrelationship between mineral compositions, modes, and the corresponding whole rock compositions.  相似文献   

2.
High‐pressure granulites are an important record of geodynamic processes in overthickened or subducted continental crust. Orthopyroxene‐free assemblages in granitic (ternary feldspar(s) + quartz + garnet + kyanite + rutile), intermediate (ternary feldspar(s) + quartz + garnet + clinopyroxene ± kyanite ±rutile ± titanite) and basic (garnet + clinopyroxene + plagioclase ± quartz + rutile) compositions indicate formation conditions at mantle depths. Clinopyroxene compositions in Variscan high‐pressure granulites are unusual in that they include omphacite (in plagioclase‐bearing rocks thus not eclogite) and Al‐rich diopside (i.e. indicating high Ca‐Tschermak content), with both yielding temperatures above 900 °C. Problems such as compositional zoning, multiple generations of key phases in reaction domains and unmixing of high‐temperature solid‐solution phases during cooling (ternary feldspars, omphacite) clearly indicate disequilibrium and require very careful interpretation as to which phases and compositions possibly represent a former equilibrium association. Pressure–temperature (P–T) determination by the pseudosection method, although allowing prediction of mineral assemblages, compositions and molar proportions for a fixed bulk composition for modelled P–T conditions, still requires reliable activity–composition information for the key phases feldspar and clinopyroxene as well as an interpretation of former equilibrium compositions in the investigated samples, i.e. the same restrictions applying to conventional thermobarometry. The interpretations of some recently determined pseudosections for the composition of Variscan clinopyroxene‐bearing high‐pressure granulites contradict numerous published P–T paths. However, quantitative information from thermobarometry or pseudosections must be integrated with key petrographic observations. In the case of the Variscan example, it is argued that petrographic observations and published P–T paths are consistent with mineral assemblages predicted in pseudosections and support existing tectonometamorphic models.  相似文献   

3.
硅酸盐体系的化学平衡:(1)物质平衡原理   总被引：6，自引：5，他引：6  
通过具体应用实例,系统介绍了在硅酸盐体系的化学平衡研究中,依据物质平衡原理,求解“相混合方程”(PME)而进行物相定量分析的“相混合计算”(PMC)方法。应用实例包括矿物原料和结晶岩物相的定量分析,复杂固溶体矿物的端员组分计算,多组分硅酸盐陶瓷的配料比例计算,以及硅酸盐陶瓷制品物相的定量分析。物相定量分析结果是结晶岩和工业岩石原料分类命名的基础,可以为改进矿物原料预处理工艺提供依据,也是研究硅酸盐体系的化学平衡、对材料制备过程进行热力学分析的基础。实际计算中必须合理估计各种分析数据的累积误差。优化计算结果的理论依据主要有矿物晶体化学原理、矿物共生组合规律和次要组分分配的固溶体矿物相优先原则。  相似文献   

4.
Chemically zoned porphyroblasts in metamorphic rocks indicate that diffusional processes could not maintain equilibrium conditions on a grain scale during porphyroblast growth or establish it afterwards. An effect of this inability to maintain equilibrium is the progressive removal of elements forming garnet cores from any metamorphic reaction that occurs at the porphyroblast boundaries or in the matrix of the rock. To examine this effect on mineral assemblages, the Bence–Albee matrix correction was applied to X‐ray intensity maps collected using eclogite samples from northern New Caledonia in order to determine the chemical composition of all parts of the sample. The manipulation of these element maps allows a quantitative analysis of the fractionation of the bulk rock composition between garnet cores and the matrix. A series of calculated equilibrium‐volume compositions represents the change in matrix chemistry with progressive elemental fractionation as a consequence of prograde garnet growth under high‐P conditions. Pressure–temperature pseudosections are calculated for these compositions, in the CaO–Na2O–FeO–MgO–Al2O3–SiO2–H2O system. Assemblages, modal proportions and mineral textures observed in the New Caledonian eclogites can be closely modelled by progressively ‘removing’ elements forming garnet cores from the bulk rock composition. The pseudosections demonstrate how chemical fractionation effects the peak metamorphic assemblage, prograde textures and the development of retrograde assemblages.  相似文献   

5.
Chemical analyses are given for Na, K, and trace elements of muscovite and potassium feldspar of granitic rocks. The distribution of trace elements in co-existing minerals suggests that equilibrium was attained and that muscovite is a primary mineral. These observations and the comparison of the trace-element chemistry of megacrysts and groundmass potassium feldspars of porphyritic rock types lead to the conclusion that the megacrysts are in face phenocrysts which crystallized in equilibrium with the other minerals of the rock.The ranges of values of the distribution coefficients KD(Rb/K) and KD(Cs/K) in mineral pairs confirm other observations on the equilibrium among various minerals. However, application of experimental data on the temperature effect on KD leads to results conflicting with the petrologic observations. The possible influence of other factors on KD is analyzed and among these factors the composition of the feldspar and the solidus-liquidus temperature interval may play a dominant role.  相似文献   

6.
发育完整的灰岩风化壳及其矿物学和地球化学特征   总被引：25，自引：5，他引：20  
对于碳酸盐岩土覆土壤成因、尽管碳酸盐岩风化残积成土说被多数学者认同,但由于碳酸盐岩中酸不溶物含量极低,在风化成土过程中会伴随着巨大的体积缩小变化,原岩结构和半风化带无法保留,从而缺失了探索上覆土壤物质来源的重要中间环节,使得这种观点缺乏野外宏观证据的支持。最近,我们在贵州、湖南等地发现了数个以泥质灰岩和泥质白云岩为基岩的碳酸盐岩风化壳剖面,尚保留有较好的原岩结构,具有明显的风化壳分带和过渡现象。这些风化壳剖面的发现为深入研究碳酸盐岩风化成土过程提供了良好的研究场所。本文选取了较为典型的吉首泥灰岩风化壳剖面,从矿物学地球化学的角度来探讨碳酸盐岩风化壳的形成过程和发育特征,结果表明该风化壳既遵循非碳酸盐岩（主要是结晶岩类）风化壳的发育特征,也具有自己独特的地球化学演化规律。风化壳总体特点受碳酸盐中的酸不溶物矿物组合及化学成分的影响甚至控制,风化非碳酸盐风壳相似的发育特征。吉首泥灰岩风化壳剖面的发育特征和作者早先提出 的碳酸盐岩风化成土的两阶段模式是一致的,即以碳酸盐矿物大量淋失、酸不溶物逐渐堆积或残积为特征的早期阶段和残积物进一步风化成土的阶段,后一阶段的演化类似非碳酸盐岩类的风化过程。  相似文献   

7.
Pumpellyite from four-phase assemblages (pumpellyite + epidote + prehnite + chlorite; pumpellyite + epidote + actinolite + chlorite; pumpellyite + epidote + Na-amphibole + chlorite, together with common excess phases), considered to be low variance in a CaO-(MgO + FeO)-Al2O3-Fe2O3 (+Na2O + SiO2+ H2O) system, have been examined in areas which underwent metamorphism in the prehnite-pumpellyite, pumpellyite-actinolite and low-temperature blueschist facies respectively. The analysed mineral assemblages are compared for nearly constant (basaltic) chemical composition at varying metamorphic grade and for varying chemical composition (basic, intermediate, acidic) at constant metamorphic conditions (low-temperature blueschist facies). In the studied mineral assemblages, coexisting phases approached near chemical equilibrium. At constant (basaltic) bulk rock composition the MgO content of pumpellyite increases, and the XFe3+ of both pumpellyite and epidote decreases with increasing metamorphic grade, the Fe3+ being preferentially concentrated in epidote. Both pumpellyite and epidote compositions vary with the bulk rock composition at isofacial conditions; pumpellyite becomes progressively enriched in Fe and depleted in Mg from basic to intermediate and acidic bulk rock compositions. The compositional comparison of pumpellyites from high-variance (1–3 phases) assemblages in various bulk rock compositions (basic, intermediate, acidic rocks, greywackes, gabbros) shows that the compositional fields of both pumpellyite and epidote are wide and variable, broadly overlapping the compositional effects observed at varying metamorphic grade in low-variance assemblages. The intrinsic stability of both Fe- and Al-rich pumpellyites extends across the complete range of the considered metamorphic conditions. Element partitioning between coexisting phases is the main control on the mineral composition at different P-T conditions.  相似文献   

8.
Palaeoproterozoic metasedimentary migmatite reflects the highest temperature parts of a regional aureole at Mt Stafford, central Australia, comprising rocks that experienced 500–800 °C at ≈3 kbar. Whole‐rock major element concentrations are correlated with Zr content, psammitic compositions having nearly twice the Zr content of pelitic compositions. Zirconium is concentrated in mesosome compared with leucosome. Zircon is largely detrital, mostly lacking any overgrowth contemporary with migmatite formation. Comparatively small proportions of micro‐zircon (<10 μm) in sub‐solidus rocks are mostly hosted by quartz and plagioclase. Much higher proportions (three to five times) of micro‐zircon in migmatite are hosted by prograde K‐feldspar, cordierite and biotite. T–X and P–T NCKFMASHTZr pseudosections constructed using thermocalc model the distribution of Zr between solid and silicate liquid phases. Half of the detrital zircon (~100 ppm Zr) is predicted to be dissolved into silicate liquid at ≈800 °C and all dissolved by 850 °C, if all zircon is involved in the equilibration volume. Melt segregation at relatively low temperature is predicted to enrich the residuum in Zr, consistent with the observed distribution of Zr between mesosome and leucosome. The limited development of metamorphic zircon rims or overgrowths at Mt Stafford is explained by three concurrent processes: (i) Zr liberated during prograde metamorphism formed micro‐zircon, rather than following the prediction that Zr will partition into silicate liquid; (ii) some detrital zircon was probably armoured by other rock‐forming minerals, reducing Zr content in the effective bulk rock composition; and (iii) small proportions of melt loss during migmatization removed Zr that otherwise would have been available to form metamorphic rims.  相似文献   

9.
Much of the exposed Archean crust is composed of composite gneiss which includes a large proportion of intermediate to tonalitic material. These gneiss terranes were typically metamorphosed to amphibolite to granulite facies conditions, with evidence for substantial partial melting at higher grade. Recently published activity–composition (a?x) models for partial melting of metabasic to intermediate compositions allows calculation of the stable metamorphic minerals, melt production and melt composition in such rocks for the first time. Calculated P?T pseudosections are presented for six bulk rock compositions taken from the literature, comprising two metabasic compositions, two intermediate/dioritic compositions and two tonalitic compositions. This range of bulk compositions captures much of the diversity of rock types found in Archean banded gneiss terranes, enabling us to present an overview of metamorphism and partial melting in such terranes. If such rocks are fluid saturated at the solidus, they first begin to melt in the upper amphibolite facies. However, at such conditions, very little (< 5%) melt is produced and this melt is granitic in composition for all rocks. The production of greater proportions of melt requires temperatures ～800–850 °C and is associated with the first appearance of orthopyroxene at pressures below 8–9 kbar or with the appearance and growth of garnet at higher pressures. The temperature at which orthopyroxene appears varies little with composition providing a robust estimate of the amphibolite–granulite facies boundary. Across this boundary, melt production is coincident with the breakdown of hornblende and/or biotite. Melts produced at granulite facies range from tonalite–trondhjemite–granodiorite for the metabasic protoliths, granodiorite to granite for the intermediate protoliths and granite for the tonalitic protoliths. Under fluid‐absent conditions the melt fertility of the different protoliths is largely controlled by the relative proportions of hornblende and quartz at high grade, with the intermediate compositions being the most fertile. The least fertile rocks are the most leucocratic tonalites due to their relatively small proportions of hydrous mafic phases such as hornblende or biotite. In the metabasic rocks, melt production becomes limited by the complete consumption of quartz to higher temperatures. The use of phase equilibrium forward‐modelling provides a thermodynamic framework for understanding melt production, melt loss and intracrustal differentiation during the Archean.  相似文献   

10.
Using continental-margin volcanic belts of East Asia as an example, the petrography and geochemistry of acid volcanic and subvolcanic rocks are considered. Cotectoid and eutectoid types are distinguished among them. The eutectoid type is characterized by a disequilibrium mineralogical composition, which includes phenocrysts of early “gabbro” paragenesis (pyroxenes, calcic plagioclase, occasional olivine and amphibole) and “granite” paragenesis (K-Na feldspar, quartz, biotite) and groundmass corresponding to dry quartz-feldspathic eutectics. A linear correlation is noted between the amount of phenocrysts of gabbro paragenesis and SiO2 content. The entire petrochemical diversity of the eutectoid-type rocks is determined by the quantitative proportions between the gabbro paragenesis and bulk composition. The cotectoid rocks are dominated by sparsely-phyric and aphyric rocks lacking melanocratic inclusions and xenogenic minerals. In the cotectoid-type rocks, the compositions of the phenocrysts and groundmass are complementary with the bulk rocks composition, indicating their equilibrium cotectic crystallization.  相似文献   

11.
The Thompson projection traditionally used by metamorphic petrologists is modified and used to study mineral equilibrium and mass balance relations of igneous rocks. Proportions of minerals in rocks and equilibrium minerals assemblages are predictable from bulk rock compositional data, consequently the projection simplifies chemical studies of plutonic and volcanic rock suites, and mixed plutonic-volcanic suites particularly, because bulk rock compositions can be directly compared with mineral compositions. As an example, changes to bulk magma compositions resulting from differentiation by crystal fractionation (Thingmuli Volcano; Red Hill Dyke) are immediately discernible and tholeiitic calc-alkaline and alkaline differentiation trends are quite distinct on the diagram. As well, minerals which have been removed from a magma during crystal fractionation generally can be identified and their compositions estimated. Magmas the compositions of which result from the mixing of two components (Kilauea Volcano) are easily identified as are the end-member mixing components of the mixed magmas.The diagram is applicable to both igneous and metamorphic rock suites, consequently it should be of particular use to those studying anataxis and granite genesis.  相似文献   

12.
Major, minor and trace element concentrations have been measured in all the volumetrically significant minerals from the L-6 chondrites Alfianello, Colby (WI) and Leedey. Most of the elements show the compositional uniformity observed in other studies. However, REE, Co and Ni are distinctly different in their abundances and their phase distributions in each of the three meteorites. Such differences must manifest differing physical and chemical conditions involved in the formation of each of the three rocks. The distributions of REE and Ni between various phases are compatible with models which assume equilibrium between presently coexisting minerals. Such a model demonstrates how plausible differences in temperature and Ni content of metallic minerals could produce the observed differences in Ni abundances in olivine and clinopyroxene from each of the three chondrites.REE are too abundant in the minerals to have been produced by crystal-liquid fractionation from a magma of whole rock composition.Alkali element abundances are incompatible with a model of closed system equilibration of the meteorites. Rb is underabundant in feldspar relative to Na when compared to the equilibrium model predictions. A portion of the Cs seems to be included in feldspar by diadochic substitution, however, significant amounts are randomly associated with other minerals, perhaps by incorporation into lattice defects and at interstices. Partial loss of this nonfeldspathic Cs may be responsible for the large range of Cs abundances observed in chondrites.  相似文献   

13.
Biotite‐muscovite‐garnet gneisses at Einasleigh contain quartz‐feldspar veins composed of the same minerals as found in the enclosing rock. The vein‐gneiss boundaries are commonly irregular and on a microscopic scale, gradational.

Certain amphibolite layers contain quartz‐feldspar veins composed of the same minerals as found in the amphibolite. Hornblende‐rich extraction zones surround these veins, and material balance calculations show that all or nearly all of the vein‐forming matter was locally derived. Variation in the abundance of hornblende and plagioclase in the amphibolite as a function of distance from a quartz‐feldspar vein can be expressed by error‐function curves, thus suggesting that the mineral‐segregation process was diffusion‐controlled. During the mineral rearrangement, the Na and Ca contents of plagioclase have evidently remained unchanged, but the vein hornblende has become slightly richer in Fe+3, Mg, and Ca, and poorer in Si and Al relative to hornblende in the adjacent amphibolite.

A certain biotite‐plagioclase rock forms layers and boudins in the gneisses and contains pegmatite veins composed of the same minerals as found in the host rock. The plagioclase in these veins is more sodic than that in the host rock while the biotite contains slightly more Ti and Fe+2 and less Si and Mg than the biotite of the enclosing rock.

The data indicate that significant portions of the vein‐forming matter at Einasleigh were locally derived. The chemistry of some minerals has changed slightly during the segregation process, resulting possibly from different diffusion rates for the different mineral‐forming constituents.  相似文献   

14.
Sapphirine, coexisting with quartz, is an indicator mineral for ultrahigh‐temperature metamorphism in aluminous rock compositions. Here a new activity‐composition model for sapphirine is combined with the internally consistent thermodynamic dataset used by THERMOCALC, for calculations primarily in K2O‐FeO‐MgO‐Al2O3‐SiO2‐H2O (KFMASH). A discrepancy between published experimentally derived FMAS grids and our calculations is understood with reference to H2O. Published FMAS grids effectively represent constant aH2O sections, thereby limiting their detailed use for the interpretation of mineral reaction textures in compositions with differing H2O. For the calculated KFMASH univariant reaction grid, sapphirine + quartz assemblages occur at P–T in excess of 6–7 kbar and 1005 °C. Sapphirine compositions and composition ranges are consistent with natural examples. However, as many univariant equilibria are typically not ‘seen’ by a specific bulk composition, the univariant reaction grid may reveal little about the detailed topology of multi‐variant equilibria, and therefore is of limited use for interpreting the P–T evolution of mineral assemblages and reaction sequences. Calculated pseudosections, which quantify bulk composition and multi‐variant equilibria, predict experimentally determined KFMASH mineral assemblages with consistent topology, and also indicate that sapphirine stabilizes at increasingly higher pressure and temperature as XMg increases. Although coexisting sapphirine and quartz can occur in relatively iron‐rich rocks if the bulk chemistry is sufficiently aluminous, the P–T window of stability shrinks with decreasing XMg. An array of mineral assemblages and mineral reaction sequences from natural sapphirine + quartz and other rocks from Enderby Land, Antarctica, are reproducible with calculated pseudosections. That consistent phase diagram calculations involving sapphirine can be performed allows for a more thorough assessment of the metamorphic evolution of high‐temperature granulite facies terranes than was previously possible. The establishment of a a‐x model for sapphirine provides the basis for expansion to larger, more geologically realistic chemical systems (e.g. involving Fe3+).  相似文献   

15.
Metamorphic fractional crystallization involves fractionation of material into the interior of a crystallizing mineral such as garnet with consequent change in the effective bulk composition. In assemblages with thermodynamic variance of 3 or greater, the mineral assemblage, compositions of coexisting phases and the zoning profile preserved in the garnet are a function of the amount of material that is fractionated. Homogenization of zoned garnet by intracrystalline diffusion at elevated temperatures operates on a time scale of millions to tens of millions of years depending on the temperature-time path and radius of the garnet. One effect of homogenization is to drive chemical reactions by a metasomatic mechanism (internal metasomatism), even in the absence of changes in pressure or temperature. This process may affect the appearance or disappearance of minerals, and may, in some rocks, be responsible for the first appearance of kyanite or the disappearance of staurolite in Barrovian terranes.  相似文献   

16.
The basement of the central Qilian fold belt exposed along the Minhe-Ledu highway consists of psammitic schists, metabasitic rocks, and crystalline limestone. Migmatitic rocks occur sporadically among psammitic schist and metabasitic rocks. The mineral assemblage of psammitic schist is muscovite + biotite + feldspar + quartz ± tourmaline ± titanite ± sillimanite and that of metabasitic rocks is amphibole + plagioclase + biotite ± apatite ± magnetite ± pyroxene ± garnet ± quartz. The migmatitic rock consists of leucosome and restite of various volume proportions; the former consists of muscovite + alkaline feldspar + quartz ± garnet ± plagioclase while the latter is either fragments of psammitic schist or those of metabasitic rock. The crystalline limestone consists of calcite that has been partly replaced by olivine. The olivine was subsequently altered to serpentine. Weak deformations as indicated by cleavages and fractures were imposed prominently on the psammitic schists, occasionally on me  相似文献   

17.
On thermobarometry   总被引：15，自引：2，他引：13  
Thermobarometry, the estimation of the pressure–temperature ( P – T ) conditions of metamorphism, can be undertaken by using pseudosection calculations as well as by conventional methods. Conventional thermobarometry uses only the equilibrium thermodynamics of balanced reactions between end-members of minerals, combined with the observed compositions of minerals. In contrast, pseudosections involve a forward calculation of mineral equilibria for a given rock composition. When related to observed rock data such as mineral assemblages, mineral proportions and mineral compositions, pseudosections have the power to provide valuable additional thermobarometric information. This is because the rock composition provides added constraints on P – T , unavailable in conventional thermobarometry, such as when minerals in the mineral assemblage are no longer stable, or when additional minerals join the mineral assemblage. Considering both conventional and pseudosection thermobarometry, a minimum requirement is that they use the same thermodynamic data and activity–composition models for the minerals involved. A new thermocalc facility is introduced that allows pseudosection datafile coding to be used for conventional thermobarometry. Guidelines are given and pitfalls discussed relating to pseudosection modelling and conventional thermobarometry. We argue that, commonly, pseudosection modelling provides the most powerful thermobarometric tools.  相似文献   

18.
Eclogites within exhumed continental collision zones indicate regional burial to depths of at least 60 km, and often more than 100 km in the coesite‐stable, ultra‐high pressure (UHP) eclogite facies. Garnet, omphacitic pyroxene, high‐Si mica, kyanite ± coesite should grow at the expense of low‐P minerals in most felsic compositions, if equilibrium obtained at these conditions. The quartzofeldspathic rocks that comprise the bulk of eclogite facies terranes, however, contain mainly amphibolite facies, plagioclase‐bearing assemblages. To what extent these lower‐P minerals persisted metastably during (U)HP metamorphism, or whether they grew afterwards, reflects closely upon crustal parameters such as density, strength and seismic character. The Nordfjord area in western Norway offers a detailed view into a large crustal section that was subducted into the eclogite facies. The degree of transformation in typical pelite, paragneiss, granitic and granodioritic gneiss was assessed by modelling the equilibrium assemblage, comparing it with existing parageneses in these rocks and using U/Th–Pb zircon geochronology from laser ablation ICPMS to establish the history of mineral growth. U–Pb dates define a period of zircon recrystallization and new growth accompanying burial and metamorphism lasting from 430 to 400 Ma. Eclogite facies mafic rock (~2 vol.% of crust) is the most transformed composition and records the ambient peak conditions. Rare garnet‐bearing pelitic rocks (<10 vol.% of crust) preserve a mostly prograde mineral evolution to near‐peak conditions; REE concentrations in zircon indicate that garnet was present after 425 Ma and feldspar broke down after 410 Ma. Felsic gneiss – by far the most abundant rock type – is dominated by quartz + biotite + feldspar, but minor zoisite/epidote, phengitic white mica, garnet and rutile point to a prograde HP overprint. Relict textures indicate that much of the microstructural framework of plagioclase, K‐feldspar, and perhaps biotite, persisted through at least 25 Ma of burial, and ultimately UHP metamorphism. The signature reaction of the eclogite facies in felsic rocks – jadeite/omphacite growth from plagioclase – cannot be deduced from the presence of pyroxene or its breakdown products. We conclude that prograde dehydration in orthogneiss leads to fluid absent conditions, impeding equilibration beyond ~high‐P amphibolite facies.  相似文献   

19.
Phase relations have been determined at 20 kbar and primarily under suprasolidus conditions in the Fe−Ti-free F-bearing K-richterite—phlogopite and K-richterite—apatite systems in order to assess the partitioning of F among phlogopite, K-richterite, apatite, and melt under upper-mantle conditions. Both systems are pseudoternary because they contain forsterite, enstatite and a diopside-rich clinopyroxene from the breakdown of the mica and K-richterite. The F-bearing K-richterite systems have lower minimum melting temperatures than the F-bearing phlogopite —apatite system at the same pressure. However in the systems studied, F in phlogopite appears the most effective component in altering minimum liquid compositions whereas comparison between the present study and previous systems suggests that the presence of P2O5 during melting may result in more K-enriched melts. Variations in the compositions of the F-bearing phases are primarily controlled by the bulk compositions of the end-member minerals and by temperature, although buffering by non-F bearing minerals (e.g. clinopyroxene) may be effective. Distribution coefficients (as wt% ratios) between F-bearing minerals and coexisting liquids have been determined as functions of bulk composition and temperature for products of experiments. Distribution coefficients between K-richterite—liquid, apatite—liquid, and phlogopite—liquid are ≥1 to slightly <1 for most bulk compositions, indicating thatF is generally a compatible element. This conclusion is in agreement with the sequence ofF distribution for similar phases in ultrapotassic rocks. These results preclude F-bearing mineral reservoirs in the mantle, at depths corresponding to 20 kbar, being capable of producing F-enrichment in ultrapotassic magmas, or being effective in redox melting processes. Editorial responsibility: K. Hodges  相似文献   

20.
REE partition data between solid phases in nine spinel peridotite xenoliths from Assab (Ethiopia) are presented together with bulk-rock REE composition. REE partitioning between clinopyroxene and other coexisting solid phases varies over a relatively wide range. The largest ranges are for LREE in clinopyroxene/orthopyroxene and clinopyroxene/olivine pairs, while clinopyroxene/spinel partitioning of REE is more restricted. The range of REE partition values between coexisting phases is due to compositional dependency effects and is correlated with systematic variations in major element composition of the bulk rocks. The measured REE concentration in the Assab mantle harzburgites do not match with the compositions calculated by mass balance from the modal proportions and REE analyses in individual phases. Inconsistencies for HREE may be due to variable HREE amounts in the clinopyroxene, orthopyroxene phases within a single specimen, while the high LREE contents in the whole rocks are due to contamination during transport to the surface. A geochemical model based on theoretical treatment of the REE partition data suggests that the Assab harzburgites acquired their residual character during a batch melting episode in the upper mantle under the Afar region.  相似文献   

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