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1.
《International Geology Review》2012,54(13):1443-1463
Fluid inclusions hosted by quartz veins in high-pressure to ultrahigh-pressure (HP-UHP) metamorphic rocks from the Chinese Continental Scientific Drilling (CCSD) Project main drillhole have low, varied hydrogen isotopic compositions (δD?=??97‰ to??69‰). Quartz δ18O values range from??2.5‰ to 9.6‰; fluid inclusions hosted in quartz have correspondingly low δ18O values of??11.66‰ to 0.93‰ (T h?=?171.2～318.8°C). The low δD and δ18O isotopic data indicate that protoliths of some CCSD HP-UHP metamorphic rocks reacted with meteoric water at high latitude near the surface before being subducted to great depth. In addition, the δ18O of the quartz veins and fluid inclusions vary greatly with the drillhole depth. Lower δ18O values occur at depths of ～900–1000 m and ～2700 m, whereas higher values characterize rocks at depths of about 1770 m and 4000 m, correlating roughly with those of wall-rock minerals. Given that the peak metamorphic temperature of the Dabie-Sulu UHP metamorphic rocks was about 800°C or higher, much higher than the closure temperature of oxygen isotopes in quartz under wet conditions, such synchronous variations can be explained by re-equilibration. In contrast, δD values of fluid inclusions show a different relationship with depth. This is probably because oxygen is a major element of both fluids and silicates and is much more abundant in the quartz veins and silicate minerals than is hydrogen. The oxygen isotope composition of fluid inclusions is evidently more susceptible to late-stage re-equilibration with silicate minerals than is the hydrogen isotope composition. Therefore, different δD and δ18O patterns imply that dramatic fluid migration occurred, whereas the co-variation of oxygen isotopes in fluid inclusions, quartz veins, and wall-rock minerals can be better interpreted by re-equilibration during exhumation.

Quartz veins in the Dabie-Sulu UHP metamorphic terrane are the product of high-Si fluids. Given that channelized fluid migration is much faster than pervasive flow, and that the veins formed through precipitation of quartz from high-Si fluids, the abundant veins indicate significant fluid mobilization and migration within this subducted continental slab. Many mineral reactions can produce high-Si fluids. For UHP metamorphic rocks, major dehydration during subduction occurred when pressure–temperature conditions exceeded the stability of lawsonite. In contrast, for low-temperature eclogites and other HP metamorphic rocks with peak metamorphic P–T conditions within the stability field of lawsonite, dehydration and associated high-Si fluid release may have occurred as hydrous minerals were destabilized at lower pressure during exhumation. Because subduction is a continuous process whereas only a minor fraction of the subducted slabs returns to the surface, dehydration during underflow is more prevalent than exhumation even in subducted continental crust, which is considerably drier than altered oceanic crust.  相似文献   

2.
Analyses of trace elements in the mineral phases of granulites provide important information about the trace element distribution in the lower crust. Since granulites are often considered residues of partial melting processes, trace element characteristics of their mineral phases may record mineral/melt equilibria thus giving an opportunity to understand the nature and composition of melts in the lower continental crust. This study provides an extensive set of mineral trace element data obtained by LA-ICP-MS analyses of mafic and intermediate granulites from Central Finland. Mass balance calculations using the analytical data indicate a pronounced contribution of the accessory minerals apatite for the REE and ilmenite for the HFSE. Coherent mineral/mineral ratios between samples point to a close approach to equilibrium except for minerals intergrown with garnet porphyroblasts. Mineral trace element data were used for the formulation of a set of D mineral/melt partition coefficients that is applicable for trace element modelling under lower crustal conditions. D mineral/melt were derived by the application of predictive models and using observed constant mineral/mineral ratios. The comparison of the calculated D mineral/melt with experimental data as well as the relationship between mineral trace element contents and a leucosome with a composition close to an equilibrium melt provides additional constraints on mineral/melt partitioning. The D values derived in this study are broadly similar to magmatic partition coefficients for intermediate melt compositions. They provide a first coherent set of D values for Sc, V, Cr and Ni between clinopyroxene, amphibole, garnet, orthopyroxene, ilmenite and melt. In addition, they emphasize the strong impact that ilmenite exerts on the distribution of Nb and Ta.  相似文献   

3.
道地药材生长与生态地球化学研究对实现中医药科学化和标准化具有重要意义。从承德市滦河流域与金沟屯和五道岭典型研究区阐明区域尺度和不同地质建造区Ge元素地球化学背景特征，结合多元统计采用基于Nb元素的质量迁移系数、化学蚀变指数CIA和残积系数RF、生物富集系数论述Ge元素在基岩-风化壳-土壤-黄芩系统中的迁移聚集规律，探讨Ge元素生态地球化学特征与道地药材黄芩的适生关系。结果表明：滦河流域表层土壤Ge元素平均含量为1.336 mg·kg-1，43.54%土壤样品Ge元素含量属丰富—较丰富水平；金沟屯和五道岭区表层土壤Ge元素平均含量分别为1.352 mg·kg-1和1.268 mg·kg-1。不同地质建造和表层土壤Ge元素含量与TFe2O3含量显著相关，土壤含铁矿物对Ge元素具有吸附作用。Ge元素含量随岩土风化程度升高而增大，金沟屯区土壤风化程度高于五道岭区，土壤成熟度相对较高，Ge元素富集程度相对较高。岩石风化过程中Ge元素与TFe2O3、V、Ti、Co、P、Pb、Cu、Zn、Al2O3、SiO2、K2O、Na2O质量迁移系数值相近，风化土壤与新鲜基岩Si和Ge含量发生明显分异，Ge元素主要来源于硅酸盐矿物风化过程中晶格破裂和金属硫化物矿物风化释放。金沟屯和五道岭黄芩Ge元素BCF平均值分别为0.014和0.020，黄芩根部对土壤Fe与Ge的吸收表现出明显的协同作用，土壤pH影响着Ge元素形态和生物有效性。区域土壤丰富的Fe、P和Sr元素含量为优质黄芩生长提供了有利条件；Fe族元素含量丰富，pH呈微碱性的沙壤质土壤为道地药材黄芩适宜生长和定向栽培种植区。  相似文献   

4.
Pyrite and arsenopyrite are the predominant ore minerals in the Korean Au-Ag deposits of this study. The X Ni py , X Co py , X Ni apy , and X Co apy values range between 100 and 3,000 ppm, 200 and 6,000 ppm, 200 and 8,200 ppm, and 100 and 10,200 ppm, respectively. Most X Ni py /X Co py values fall in the field lower than values varying 0.16–1.30. Arsenopyrite also tends to prefer cobalt rather than nickel showing X Ni apy /X Co apy values between 0.20 and 1.40. The concentrations of minor elements in ores and gangue minerals vary 1–55 ppm Au and 1–1,120 ppm Ag for the former and 4–57 ppm Ni and 2–45 ppm Co for the latter. The Au/Ag ratio in ore has a good correlation to the Ni/Co ratio of arsenopyrite to gangue. The (Ni/Co)py-(Ni/Co)gangue and (Ni/Co)apy-(Ni/Co)gangue diagrams revealed that the values from the Korean Au-Ag deposits plot in the field lower than 900 °C which is the lowermost temperature determined by previous partitioning experiments.  相似文献   

5.
Iron-magnesium distribution coefficients for coexisting ortho- and clinopyroxene in 22 amphibolites from the New Jersey Precambrian Highlands range from 1.40 to 1.90. No systematic areal variation of the distribution coefficient is discernable within a 700 mi2 area. The distribution coefficient is, however, systematically related to pyroxene composition. The distribution coefficient tends to increase with increasing pyroxene weight % FeO (Fe as FeO) and decrease with increasing MgO and Al2O3. Data from other workers indicates that the distribution coefficient versus pyroxene composition trends found in the Highlands amphibolites are also present in both igneous and metamorphic rock suites from several other areas. Possible influence of pyroxene CaO on the distribution coefficient is also indicated. The Highlands amphibolite type trends are, however, directly opposite to those previously reported for Australian granulites. Both types of trends are apparently valid since both are present in at least one instance in metamorphic rocks from a relatively small area. The causes for the development of the two types of trends are imperfectly understood. Data presented indicates, however, that the New Jersey amphibolite type trends are apparently more characteristic of Fe-poor pyroxenes, whereas, the Australian granulite type trends are more characteristic of Fe-rich pyroxenes.The distribution coefficient in the Highlands amphibolites is also systematically related to bulk-rock composition due to the sympathetic variation of pyroxene Fe-Mg content with total rock MgO/FeO(Fe as FeO). The observed range of the distribution coefficient in the Highlands amphibolites may, consequently, mostly reflect variation in bulk-rock composition and not variation in crystallization temperature.  相似文献   

6.
The partitioning of Sr between calcite, dolomite and liquids is essentially independent of temperature between 150° and 350° C. The partition coefficients corrected for number of cation sites are b calc=0.096 and b dol= 0.048 for 1 mol cations/6 mol H2O liquid. Upon dilution the partition coefficients increase, but their ratio stays constant at about 2∶1. This ratio is due to the fact that calcite has twice as many Ca-sites for Sr-substitution as dolomite. The 2∶1 relationship is also observed in natural calcite and dolomite which have undergone diagenesis. The temperature independence of partitioning is caused by the relatively small thermal expansion of calcite and dolomite. Thermal expansion between 25° and 400° C was found to follow the equations V calc=7.0·10−4 T(°C)+36.95 and V dol=6.9·10−4 T(°C)+32.24, V: cm3/mol. Therefore calcite and dolomite cannot serve as a temperature indicator. To have an ideal geothermometer a mineral pair with high and low thermal expansion is required. Literature date demonstrate that wurtzite, sphalerite, and galena are such minerals.  相似文献   

7.
The oxygen and carbon isotopic compositions of Upper Cretaceous chalk have been studied from a large number of outcrops and boreholes in the Danish sub-basin and the North Sea Central Graben. The carbon isotopic compositions vary from +0.50%o to +3.00%oδ13C which correspond to the expected carbon isotopic composition of carbonate precipitated from normal sea water. The oxygen isotopic compositions of samples from outcrops and near-surface drilled sections fall in the range from —0.50%o to — 2.00%oδ18O, which is close to the expected values for carbonate produced by coccoliths in the Late Cretaceous sea. A geographic distribution exists in the Danish sub-basin showing relatively heavy oxygen isotope values in the centre of the basin and slightly more negative values in the eastern part of the basin. Primarily the phenomenon is thought to reflect minor variations in the oceanographic parameters in the Late Cretaceous sea. The deep subsurface sections represent a depth interval of 0–3100 m. Mechanical compaction in the uppermost part of the sequences apparently has no influence on the isotopic composition. Chemical compaction dominates at greater depth, leading to temperature-induced isotopic re-equilibration in the water-rock system. In these sequences the oxygen isotope values range from ? 1.50%o to — 7.50%oδ18O and are significantly correlated with depth of burial, cementation and porosity. The data indicate that pressure-dissolution, recrystallization, reprecipitation and ion-exchange between solid carbonate phase and pore water, are all actively involved in the oxygen isotope re-equilibration process. This process is believed to take place in a diagenetically closed system and is tentatively divided into two phases: 1) an early diagenetic phase which takes place at porosities down to approximately 20% in which the chalk possesses a pore-water controlled isotopic re-equilibration system and 2) a late diagenetic phase at porosities below 20% in which the re-equilibration process increasingly becomes influenced by the rock-introduced isotopic change in the composition of the formation water.  相似文献   

8.
The mobility of strontium in subsurface is largely influenced by sorption on to clay minerals. In the present study, kaolinite clay samples collected from the Kalpakkam nuclear plant site were employed to understand the sorption characteristics of strontium by batch method. The effect of several parameters such as time, strontium ion concentration, pH, temperature and ionic strength was investigated. The kinetic studies suggested pseudo-second-order mechanism. The experimental sorption data was fitted to Langmuir adsorption model for obtaining the sorption capacity of the sorbent. The maximum sorption capacity was 5.77 mg/g at 298 K and was found to increase with an increase in temperature. It was observed that the distribution coefficient (K d) of strontium on clay increased as the pH of the solution increased. The distribution coefficient was found to decrease with an increase in concentration of Na+ and Ca2+ ions. This variation of K d suggests that cation exchange is the predominant sorption process. It was also observed that sorption process is endothermic. The thermodynamic parameters such as ∆G 0, ∆H 0 and ∆S 0 were calculated. The negative values obtained for ∆G 0 indicated that the sorption of strontium on clay was spontaneous at all studied concentrations. ∆G 0 becomes more negative with an increase in temperature, suggests that the sorption process is more favorable at higher temperatures.  相似文献   

9.
The effect of silicate liquid structure upon mineral-liquid partitioning has been investigated by determining element partitioning data for coexisting immiscible granitic and ferrobasaltic magmas. The resulting elemental distribution patterns may be interpreted in terms of the relative states of polymerization of the coexisting magmas. Highly charged cations (REE, Ti, Fe, Mn, etc.) are enriched in the ferrobasaltic melt. The ferrobasaltic melt is relatively depolymerized due to its low SiO ratio. This allows highly charged cations to obtain stable coordination polyhedra of oxygen within the ferrobasaltic melt. The granitic melt is a highly polymerized network structure in which Al can occupy tetrahedral sites in copolymerization with Si. The substitution of Al+3 for Si+4 produces a local charge imbalance in the granitic melt which is satisfied by a coupled substitution of alkalis, thus explaining the enrichment of low charge density cations, the alkalis, in the granitic melt. P2O5 increases the width of the solvus and, therefore, the values of the distribution coefficients of the trace elements. This effect is attributed to complexing of metal cations with PO4?3 groups in the ferrobasaltic melt.The values of ferrobasalt-granite liquid distribution coefficients are reflected in distribution coefficients for a mineral and melts of different compositions. The mineral-liquid distribution coefficient for a highly charged cation is greater for a mineral coexisting with a highly polymerized melt (granite) than it is for that same mineral and a depolymerized melt (ferrobasalt). The opposite is true for low charge density cations. Mineralliquid and liquid-liquid distribution coefficients determined for the REE's indicate that fractionated REE patterns are due to mineral selectivity and not the state of polymerization of the melt.  相似文献   

10.
Distribution coefficients (K D·Fe ++ –Mg) calculated for orthopyroxene-clinopyroxene pairs from 12 basic granulites of the Quairading district, Western Australia, range from 1.87 for magnesian pyroxenes (Opx Mg value=78.1) to 1.70 for iron-rich varieties (Opx Mg value 37.7). Field and petrographic evidence indicates that these pyroxenes have probably reached equilibrium within a narrow temperature range. In order to account for the observed variation of K D values it is suggested that one (or both) of the pyroxene structures is not the ideal Fe++-Mg solution proposed in the thermodynamic model of the pyroxene equilibrium exchange. After consideration of the geometry of the pyroxene cation sites, the relative bond energies of each site (especially crystal field stabilization energy) and structural ordering a model is proposed to explain the non-ideal behaviour of Fe++-Mg in the pyroxene system. The distribution pattern in low-iron pyroxenes will probably show Fe++ favouring the M 2·Opx site; competing unfavourably with Mg++ for the M 1·Cpxsite; and probably excluded by Mg++ from the M 1·Opxsite. As the iron content of the system increases the M 2·Opxsite will begin to become saturated with Fe++ and this ion will enter the M 1·Opx site. Further increases in the iron content of the system will cause the Fe++-Mg distribution to depend increasingly on the relative attraction of the M 1 sites of both pyroxenes. Of these sites Fe++ should show preference to the more distorted M 1·Cpxsite. The distribution coefficient reflects this swing towards a relative enrichment of Fe++ in the clinopyroxene by decreasing regularly with increasing iron content. It is likely that this downward trend will not become evident until the iron content of the M 2·Opx site reaches saturation. This would explain why the K D values for the magnesian pyroxenes remain practically unchanged until the orthopyroxene Mg value is approximately 60; from here on the iron-rich pyroxenes show a rapid decrease in K D value with increasing iron content.The Ca content of the pyroxenes is also significant since the Quairading pyroxenes show a marked increase in mutual solubility with increasing iron content. Calcium taken into the orthopyroxene structure will enter the M 2 site ahead of Fe++ so that this site will reach Fe++ saturation at a lower iron content than when the orthopyroxene is Ca-free.The application of K D values to the regional study of basic granulites, particularly when establishing relative temperature zones on the basis of K D variation, should only be attempted when pyroxenes which extend over a wide range of Fe-Mg content are available.  相似文献   

11.
Hercynian S-type granites from the southeastern Schwarzwald granite series represent cogenetic biotite-and two-mica granites. Oxygen- and hydrogen-isotope data show that hydrothermal alteration invoking isotopically light surface waters resulted in a drastic reduction in 18O and D and pronounced disequilibrium between the minerals. Effective water-rock ratios are calculated to be high, about 0.8 vol units. A shift in the18O/16O and the chemical composition of the fluid due to water-rock interaction is continuously traced from pure H2O with meteoric isotopic character in the deep-seated biotite granites to slightly saline water with rock-equilibrated isotopic composition in the two-mica granites at a shallower level. Substantial retrograde hydrometamorphism in the temperature range 500° to 200° C resulted mineralogically in high-temperature chloritization of biotite, and low-temperature muscovitization as well as feldspar alteration, respectively. Another result of the re-equilibration of cations is strong disturbance of the Rb–Sr system which affects measured ages and initial87Sr/86Sr values. Hydrothermal differentiation and alteration probably overlap to a very large extent magmatic differentiation processes.  相似文献   

12.
1 Introduction It has been understood in the study of terrestrial heat flow that the distribution of heat flow in the interior of continent is influenced by a large number of factors, involving heat sources (e.g. mantle heat flow, heat production of radioactive elements in the crust, magmatic activity, and heat production of tectonic deformation), heat transfercondition (e.g. thermal conductivity and thickness of media), groundwater circulation, etc. On the background of these factors it is pa…  相似文献   

13.
Optical constituents as suspended particulate matter (SPM), chlorophyll (Chl-a), colored dissolved organic matter (CDOM), and grain sizes were obtained on a transect in the arctic fjord-type estuary Kangerlussuaq (66°) in August 2007 along with optical properties. These comprised diffuse attenuation coefficient of downwelling PAR (K d(PAR)), upwelling PAR (K u(PAR)), particle beam attenuation coefficient (c p), and irradiance reflectance R(−0, PAR). PAR is white light between 400 and 700 nm. The estuary receives melt water from the Greenland Inland Ice and stations covered a transect from the very high turbid melt water outlet to clear marine waters. Results showed a strong spatial variation with high values as for suspended matter concentrations, CDOM, diffuse attenuation coefficient K d(PAR), particle beam attenuation coefficients (c p), and reflectance R(−0, PAR) at the melt water outlet. Values of optical constituents and properties decreased with distance from the melt water outlet to a more or less constant level in central and outer part of the estuary. There was a strong correlation between inorganic suspended matter (SPMI) and diffuse attenuation coefficient K d(PAR) (r 2 = 0.92) and also for particle beam attenuation coefficient (c p; r 2 = 0.93). The obtained SPMI specific attenuation—K d*(PAR) = 0.13 m2 g−1 SPMI—and the SPMI specific particle beam attenuation—c p* = 0.72 m2 g−1—coefficients were about two times higher than average literature values. Irradiance reflectance R(−0, PAR) was comparatively high (0.09−0.20) and showed a high (r 2 = 0.80) correlation with K u(PAR). Scattering dominated relative to absorption—b(PAR)/a(PAR) = 12.3. Results strongly indicated that the high values in the optical properties were related to the very fine particle sizes (mean = 2–6 μm) of the suspended sediment. Data and results are discussed and compared to similar studies from both temperate and tropical estuaries.  相似文献   

14.
Studies of the compositions of coexisting sulphide assemblages from certain Zambian Copperbelt deposits and of their textural relations and host rock environments have been undertaken by routine microscopy and using electron microprobe analysis. Special attention has been paid to sulphide assemblages containing cobalt. Using experimental data on the systems Cu-Co-S, Cu-Fe-Co-S and on sulphidation equilibria, together with the available information on equilibria involving gangue minerals and some new calculations, an attempt has been made to define the chemical conditions of ore formation and/or re-equilibration in several deposits (Baluba, Chibuluma West and Chibuluma, Chambeshi S.E.). If a re-equilibration temperature of 300°C is assumed the range of aS2 prevailing during final formation of the assemblages was of the order 10–7 – 10–9 atm, more rarely dropping to 10–11 – 10–12 atm. If magnetite is present, and this is considered very unlikely in most cases, aO2 may have reached as high as 10–35 atm but it is generally likely to have been around 10–50 atm or even lower. Values of aCO2 are assumed to have been of the order of 10–0.5 atm. Detailed studies of drill hole samples from the Chambeshi S.E. deposit suggest an important link between the petrology of the host rocks and the sulphide mineral chemistry. In particular, the control exerted on sulphide composition by aS2 may have been related to the availability of sulphate in the form of diagenetic anhydrite or in sulphate-rich interstitial waters. The distinctive distribution of cobalt in the ores appears related to the distribution of amphibolite bodies and in turn to rift fault systems in the Basement which allowed upward movement of fluids enriched in magmatically derived cobalt.  相似文献   

15.
To assist in the assignment and interpretation of 23Na NMR spectra in silicate and aluminosilicate minerals and glasses we have calculated the 23Na NMR shieldings and the electric field gradients (EFG) at the Na for a number of Na-containing species. Included are Na(OH2) n +, n = 1, 2, 4, 5, 6 and 8, and Na+ complexes with SiH3OH, SiH3ONa and O(SiH3)2. We have also evaluated shieldings and EFGs for Na-centered clusters extracted from crystalline Na2SiO3 and anhydrous sodalite, Na6[AlSiO4]6. Using 6-31G* SCF optimized geometries and the GIAO method with a 6-31G* basis set [and 6-311(2d,p) bases for the smaller clusters] we find a calculated increase in shielding with coordination number (CN) for the Na(OH2) n +, n = 4, 6, 8 series that agrees reasonably well with experimental trends. Calculated changes in the Na shielding as water is replaced by bridging or nonbridging silicate O atoms are also consistent with experimental observations. The deshielding of Na (with respect to gas-phase Na+) which is produced by an O-containing ligand is a strongly decreasing function of the R(Na–O) and a weakly decreasing function of the underbonding or free valence of the O. Deshielding contributions to the isotropic shielding from different ligands are additive to good approximation for low CN species, so that the total deshielding can be calculated accurately by summing the contributions from the individual ligands. However for the larger CN species the directly calculated deshieldings are substantially smaller than those obtained using such an additivity approximation. We further test this approximation by calculating the deshieldings for Na in 12 different sites in silicate and aluminosilicate minerals which have recently been studied experimentally, using our calculated deshielding contributions for individual O-containing ligands and experimental values for the Na–O distances. Correlation coefficients between the experimental shifts and the calculated deshieldings are around 0.9 and the slope of the correlation is almost 1.0 . Calculations on large Na-centered clusters extracted from the crystal structures of Na2SiO3 and anhydrous sodalite reproduce the experimental values for both NMR shieldings and electric field gradients but at considerable computational cost. Comparison with recent 23Na NMR studies on hydrous albite glasses indicates that coordination of either H2O or OH− to the Na could give the magnitude of deshielding observed, depending upon the detailed Na–O distances within the hydrous glass. Received: 31 December 1998 / Revised, accepted: 11 May 1999  相似文献   

16.
A method is proposed for adjusting the mass balance to characterize quantitatively the behaviour of minerals in anatexis. The method is based on an unconstrained simple mixing model that can be expressed as: where B , A 0, and A 1-n, are compositional vectors of segregate, source rock and source minerals, respectively. The most important concepts are: (1) degree of partial fusion: FMM= 1/a0; (2) mineral fractionation index: and (3) plagioclase differentiation index: . For a given mineral, the MFI values have the following meaning: (a) MFI <0: residual phase originated, at least partly, as a product of incongruent melting; (b) 0 > MFI <1: preferential retention in the residue; (c) MFI= 1: identical modal fraction in source and melt; (d) a0 > MFI > 1: preferential incorporation into the segregate, and (e) MFI > a0: external contribution to the anatectic system defined by a0 A 0. To test the method and illustrate its use, it was applied to two real problems of partial melting in the Peña Negra Anatectic Complex (Central Spain). The first is a very simple case of segregation of a diktyonitic neosome from an orthogneiss through partial melting located in vertical shear zones. This process is characterized by: (1) FMM= 0.51; (2) active incorporation of K-feldspar, plagioclase and biotite into the segregate; (3) disequilibrium melting of plagioclase; (4) residual behaviour of quartz and ilmenite. The second case concerns the formation of a cordierite-bearing granite from granodioritoid diatexites through an anatectic process, whose most salient characteristics are: (1) FMM= 0.45; (2) incongruent melting of biotite; (3) residual behaviour of plagioclase, which melted with a PDI of 1.22; (4) preferential incorporation of quartz into the segregate; (5) total extraction of K-feldspar from the residue.  相似文献   

17.
The distribution of rare earth elements (REE) between clinopyroxene (cpx) and basaltic melt is important in deciphering the processes of mantle melting. REE and Y partition coefficients from a given cpx-melt partitioning experiment can be quantitatively described by the lattice strain model. We analyzed published REE and Y partitioning data between cpx and basaltic melts using the nonlinear regression method and parameterized key partitioning parameters in the lattice strain model (D 0, r 0 and E) as functions of pressure, temperature, and compositions of cpx and melt. D 0 is found to positively correlate with Al in tetrahedral site (Al T ) and Mg in the M2 site (MgM2) of cpx and negatively correlate with temperature and water content in the melt. r 0 is negatively correlated with Al in M1 site (AlM1) and MgM2 in cpx. And E is positively correlated with r 0. During adiabatic melting of spinel lherzolite, temperature, Al T , and MgM2 in cpx all decrease systematically as a function of pressure or degree of melting. The competing effects between temperature and cpx composition result in very small variations in REE partition coefficients along a mantle adiabat. A higher potential temperature (1,400°C) gives rise to REE partition coefficients slightly lower than those at a lower potential temperature (1,300°C) because the temperature effect overwhelms the compositional effect. A set of constant REE partition coefficients therefore may be used to accurately model REE fractionation during partial melting of spinel lherzolite along a mantle adiabat. As cpx has low Al and Mg abundances at high temperature during melting in the garnet stability field, REE are more incompatible in cpx. Heavy REE depletion in the melt may imply deep melting of a hydrous garnet lherzolite. Water-dependent cpx partition coefficients need to be considered for modeling low-degree hydrous melting.  相似文献   

18.
The Yandangshan syenite is a representative Late Cretaceous igneous pluton cropping out in SE China. U–Pb zircon dating using LA‐ICP‐MS yielded a crystallization age of 98±1 Ma for the syenite. Petrographically and geochemically of shoshonitic affinity, it is enriched in LREE and LILE, and has a pronounced Nb–Ta trough in the primitive mantle‐normalized trace element spider diagram. Zircon ?Hf(t) values vary from ?3.04 to ?7.71, displaying a unimodal distribution. The syenite also has high Sr [(87Sr/86Sr) i  = 0.7086–0.7089], low Nd [?Nd(t) = ?6.57 to ?7.64] isotopic ratios, plotting in the enriched mantle field on an ?Nd(t) versus (87Sr/86Sr) i diagram. We propose that the Yandangshan syenite was generated by pyroxene‐dominated high‐pressure fractional crystallization from basaltic magma that was derived from an enriched mantle source. Although coexisting Yandangshan rhyolites have Sr–Nd isotopic compositions similar to the Yandangshan syenite, they were not derived from the same source. Instead, the rhyolitic magma was produced by partial melting of crustal materials as a result of the underplating of basaltic magma. The crust‐like Sr–Nd–Hf isotopic signature of the Yandangshan syenite is ascribed to mantle sources that were enriched by subducted sediments. Formation of Yandangshan syenite may represent roll‐back of the subducting palaeo‐Pacific plate and migration of the arc front to the Yandangshan area at ～98 Ma.  相似文献   

19.
Grandite garnet-rich calcsilicate rocks from the Lower Calcsilicate Unit of the regionally metamorphosed Reynolds Range Group (central Australia) crop out along a strike-parallel section in which a transition zone from M22 amphibolite to granulite facies rocks is exposed. Across this transition the grandite-rich layers do not show systematic changes in mineral assemblages, compositions and modes, or stable isotope compositions. These layers are deformed by F22 folds that are associated with the peak of regional low-pressure/high-temperature metamorphism. Therefore, the grandite-rich layers appear to pre-date regional metamorphism and to have acted as closed chemical systems during prograde M22 metamorphism. Mineral assemblages in the grandite-rich layers are consistent with their formation through the infiltration of oxidized, water-rich fluids (Xco2 < 0.1–0.3; log fo2 -16 to -14). The stable isotope values of calcite (Δ13C=-4.2 to -0.8%0 PDB; Δ18O = 10.5–14.0%0 V-SMOW) and bulk-silicate fractions (Δ18O = 6.1 to 10.8%) of the grandite-rich layers are most consistent with the infiltrating fluid being from a magmatic source. It is most likely that fluid infiltration occurred during the pre-M22 contact metamorphism (M21) that affected much of the Reynolds Range Group. The preservation of these assemblages is probably due to their high variance and little pervasive fluid-rock interaction having occurred during M22. The clinopyroxene- and feldspar-rich calcsilicate rocks that host the grandite-rich layers contain poikiloblastic grandite garnet that formed during prograde M22 metamorphism. Thin marbles that locally occur with the grandite-rich layers contain a third garnet generation that is post- or late M22. This grossular-rich garnet occurs in coronas around calcite, plagioclase, clinopyroxene, wollastonite and scapolite. These coronas are consistent with cooling and/or compression. However, because the marble assemblages are themselves overprinted by M21 grandite-rich layers the development of coronal garnet does not reflect a continuous P-T-t path. Rather, it more probably reflects the partial re-equilibration of M21 contact metamorphic assemblages to post-M22 conditions.  相似文献   

20.
Photoabsorption by systems of hydrogen atoms and protons in the solar photosphere is studied. Analytical formulas for the partial cross sections for photodissociation of the H 2 + molecular ion are derived for the cases of fixed vibrational-rotational energy levels and averaging over a Boltzmann distribution for a given temperature. The photoabsorption coefficients for bound-free and free-free transitions of H-H+ in the solar photosphere are calculated. These are compared with the absorption coefficients for photo-ejection of an electron from a negative hydrogen ion H? and free-free transitions of an electron in the field of a hydrogen atom H. Results can be applied to the Sun and hotter stars.  相似文献   

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