Oxygen isotope fractionation and disequilibrium displayed by some granulite facies rocks from the Fraser Range,Western Australia

The granulites of the Fraser Range are assumed to have formed in a carbon-rich fluid, and are generally devoid of hornblende, and lack obvious hydrous retrograde features. In these granulites, pyroxene, garnet, plagioclase and quartz are the minerals most likely to retain the oxygen isotope ratios fixed at an early stage of initial granulite metamorphism. Temperature estimates using these minerals commonly suggest that oxygen isotopic exchange ceased in the range 600 to 680°C. The peak metamorphic temperature was probably ～ 850°C as based on the stability fields of the coexisting minerals and some cation temperatures from coexisting pyroxenes in these rocks. Ilmenite may be slightly out of isotopic equilibrium with the other minerals. Thus, grains of quartz, feldspar, pyroxene and ilmenite have suffered considerable oxygen isotopic exchange during the retrogressive phase of the metamorphism, in spite of the fact that very little water was present in these granulites. The observed deviation from the peak metamorphic temperatures can be explained by essentially closed system solid-state diffusion (on at least a scale of centimetres) during slow cooling of the rocks from ~850 to 650°C, followed by more rapid cooling down to ～ 300°C. Such an explanation is not at variance with the radiometric data available for rocks from the area, which suggest that the latter phase could have involved uplift rates of ?0.5 mm/yr for a period of about 40 Ma. Wholerock δ¹⁸O values on non-quartzose mafic granulites, about 7.2%., fall within the range of basalts affected by seafloor weathering.     

四平山门银矿硫同位素地质特征

山门银矿的成矿热液体系中总硫同位素组成近于陨硫值与岩浆硫值相近,具深源硫特点。金属矿物硫同位素组成在同位素交换平衡条件下属中低温环境沉淀。同位素变异时间、空间上都有较明显的演化规律。     

Phase Equilibria in the Metamorphic Rocks of St. Paul Island and Cape North, Nova Scotia

A suite of schists—one from the garnet zone, 19 from thestaurolite zone, 2 from the kyanite isograd, and one from thekyanite zone—were separated into their constituent minerals.Chemical analyses of one chlorite and of 23 sets of coexistingbiotites and garnets were carried out by photometric and titrametricprocedures. Plots of garnet-biotite tie-lines from divariantassemblages on appropriate phase diagrams result in intersectingtie-lines which cannot be ascribed to experimental error. Theoreticalconsiderations argue that at equilibrium, at the same pressureand temperature or at constant pressure and varying temperature,tie-lines of divariant assemblages should not intersect. Possibleexplanations require that diffusion equilibrium of Fe and Mgbe restricted to volumes smaller than that of a hand specimenor that P as well as T varies considerably. Emission spectrographicdeterminations of Fe and Mg in biotite indicate that the Fe/Mgratio varies among biotites little more than a centimeter apart.Such a variation would argue more in favor of a lack of diffusionequilibrium.     

Diffusion control of garnet growth,Harpswell Neck,Maine, USA

A detailed analysis of chemical zoning in two garnet crystals from Harpswell Neck, Maine, forms the basis of an interpretation of garnet nucleation and growth mechanisms. Garnet apparently nucleates initially on crenulations of mica and chlorite and quickly overgrows the entire crenulation, giving rise to complex two‐dimensional zoning patterns depending on the orientation of the thin section cut. Contours of Ca zoning cross those of Mn, Fe and Mg, indicating a lack of equilibrium among these major garnet constituents. Zoning of Fe, Mg and Mn is interpreted to reflect equilibrium with the rock matrix, whereas Ca zoning is interpreted to be controlled by diffusive transport between the matrix and the growing crystal. Image analysis reveals that the growth of garnet is more rapid along triple‐grain intersections than along double‐grain boundaries. Moreover, different minerals are replaced by garnet at different rates. The relative rate of replacement by garnet along double‐grain boundaries is ordered as muscovite > chlorite > plagioclase > quartz. Flux calculations reveal that replacement is limited by diffusion of Si along double‐grain boundaries to or from the local reaction site. It is concluded that multiple diffusive pathways control the bulk replacement of the rock matrix by garnet, with Si and Al transport being rate limiting in these samples.     

Clinopyroxene-matrix partitioning of K,Rb, Cs,Sr and Ba

Extremely pure samples of clinopyroxene phenocrysts from two volcanic rocks have been analyzed for K, Rb, Cs, Sr and Ba. In conjunction with matrix concentrations, partition coefficients are obtained which are in the range 0.001–0.004 for K, Rb, Cs and Ba. These values are lower than those in the literature by factors of 6–100 but are in good agreement with values determined experimentally at pressures of 15–30 kb by Shimizu (Geochim. Cosmochim. Acta38, 1974). Values for partition coefficients measured on separates of impure or cloudy pyroxenes from these same rocks were higher and similar to those in the literature. We suggest this effect is related to ‘trapping,’ during crystal growth, of liquid which is enriched in the larger ions (such as Rb and Cs) due to lack of diffusion equilibrium in the liquid. Partition coefficient values for olivine and plagioclase from one of these same rocks were also determined.     

岩质滑坡稳定性有限元分析

目前国内外大多数规范中推荐或者强制性规定滑坡稳定性分析采用极限平衡法。由于极限平衡法本身的局限性,存在诸多不合理之处,如何对其进行改进使之更加合理已成为岩土工程中的重要课题之一。针对岩质滑坡存在明显的软弱滑动带的特点,提出了有限元计算过程中不同滑动带的处理方法,结合工程中常用的不平衡推力传递法,给出了滑坡稳定性的有限元分析方法,将其应用于芡草沱滑坡,并与基于刚体极限平衡原理的不平衡推力传递法的计算结果进行了比较,表明其计算方法可靠,可直接应用于实际工程。     

Yield design of dry‐stone masonry retaining structures—Comparisons with analytical,numerical, and experimental data

Over the past few years, there has been a steady increase in the interest in dry‐stone walling not only to preserve existing constructions but also to build new ones. Yet, dry masonry's expansion is slowed down by the lack of scientific knowledge to assess its reliability. This study aims at contributing to the construction of this scientific frame using a simplified model based on yield design and homogenization, which can be directly exploited for engineering purposes. A new analytical expression of the ultimate load is thus established. Then, the validity of the method is assessed by comparisons with limit equilibrium analysis, distinct element method, and field trials. Finally, possible improvements of the model are discussed. Copyright © 2008 John Wiley & Sons, Ltd.     

Correction to: Zeolite containing rocks of kudurs and reasons of geophagy within the territory of Sikhote-Alin Nature Zapovednik,Far East of Russia

This paper establishes a mechanical model of the stress distribution in front of the driving face during coal roadway excavation. Theoretical research shows that the stress state in the plastic zone of the driving face is consistent with the limit equilibrium equation, and the elastic zone is in accordance with the equilibrium equation based on elasticity mechanics. Based on this improved mechanical state solution model, different coal material constitutive hypotheses are used for the analysis. The width of the plastic zone calculated under the brittle-perfectly elastic model can reach 2–5 times the height of the roadway, and the stress concentration coefficient can reach two or more times. 3DEC numerical simulation software was used to simulate the stress distribution of the heading face. The results of the simulation are similar to those of the theoretical analysis. Compared with the elastic-perfectly plastic model, the calculated results of the brittle-perfectly elastic model are more consistent with the numerical simulation results. The heading face coal during roadway excavation shows obvious damage, and the strength characteristics of the coal decrease.     

Geochemistry of sodic waters in the Datong intermountain basin,Shanxi Province,northwestern China

The paper presents a critical analysis of current concepts of the origin of sodic waters. The example of the Datong Basin with widespread sodic waters is employed to demonstrate that these waters typically have salinities of 0.6–4.5 g/l at pH of 7.8–8.8. It was determined that sodic waters are in equilibrium with calcite and clay minerals (montmorillonite and kaolinite) and, sometimes, also with analcime but are never in equilibrium with anorthite, albite, forsterite, microcline, and muscovite; i.e., the water-rock system is in equilibrium-unequilibrium state. The degree of evaporation concentration of salts is in places as high as a few tens. The complex analyses of conditions under which sodic waters are formed indicates that these waters are produced during a certain weathering stage of aluminosilicates, after the groundwaters have reached equilibrium with calcite. The time when this equilibrium can be reached is controlled by the intensity of the water exchange. Original Russian Text ? S.L. Shvartsev, Yanxing Wang, 2006, published in Geokhimiya, 2006, No. 10, pp. 1097–1109.     

The behavior of Mg, Fe, and Ni during the replacement of olivine by orthopyroxene: experiments relevant to mantle metasomatism

Replacement of olivine by orthopyroxene is a frequently observed phenomenon in mantle metasomatism. In order to study element redistribution in SiO₂ metasomatism we synthesised orthopyroxene reaction rims at the contacts between forsterite-rich olivine and quartz. The orthopyroxene rims grew from the original quartz-olivine interface into both directions implying counterdiffusion of iron/magnesium and silicon. Following local equilibrium partitioning the X_Fe is lower in the orthopyroxene than in the reactant olivine at the olivine-orthopyroxene replacement front. The resulting local iron excess is compensated by formation of orthopyroxene with a higher X_Fe at the quartz-orthopyroxene interface, which is out of equilibrium with the reactant olivine. This is facilitated through short circuit diffusion along grain boundaries within the orthopyroxene rim. Due to the low capacity of orthopyroxene to accommodate Ni, this component is forced to diffuse back into the olivine producing a Ni enriched zone ahead of the replacement front. This leads to Ni contents in the orthopyroxene rim, which are higher than what is expected in equilibrium with the unaltered olivine. Taking quartz as a proxy for a silica rich fluid or liquid metasomatising agent, we conclude that the overall element fractionation between olivine and the silica rich phase may deviate from equilibrium partitioning so that the Fe and Ni concentrations in the orthopyroxene which is in contact with quartz are higher than in equilibrium with the reactant olivine. This indicates that kinetic fractionation is important for the chemical evolution of both the mantle rocks and the metasomatising agents.     

基于强度折减系数法的基坑数值仿真分析

研究表明,由极限平衡法确定的滑动面、安全系数存在一定误差,强度折减法以弹塑性力学为基础,能准确给出真实稳定系数的下限。本文以武汉某基坑为例,以强度折减法为基础,采用flac软件进行数值仿真分析,提出了基坑支护的方法,经过工程验证,达到了预期的支护效果。     

The partial equilibration of garnet porphyroblasts in pelitic schists and its control on prograde metamorphism,Glen Roy,Scotland

Garnet porphyroblasts in sillimanite‐bearing pelitic schists contain complex textural and compositional zoning, with considerable variation both within and between adjacent samples. The sillimanite‐bearing schists locally occur in regional Barrovian garnet zone assemblages and are indicative of a persistent lack of equilibrium during prograde metamorphism. Garnet in these Dalradian rocks from the Scottish Highlands preserves evidence of a range of metamorphic responses including initial growth and patchy coupled dissolution–reprecipitation followed by partial dissolution. Individual porphyroblasts each have a unique and variable response to prograde metamorphism and garnet with mainly flat compositional profiles co‐exists with those containing largely unmodified characteristic bell‐shaped Mn profiles. This highlights the need for caution in applying traditional interpretations of effective volume diffusion eliminating compositional variation. Cloudy garnet with abundant fluid inclusions is produced during incomplete modification of the initial porphyroblasts and these porous garnet are then particularly prone to partial replacement in sillimanite‐producing reactions. The modification of garnet via a dissolution–reprecipitation process releases Ca into the effective whole‐rock composition, displacing the pressure–temperature positions of subsequent isograd reactions. This represents the first report of internal metasomatism controlling reaction pathways. The behaviour of garnet highlights the importance of kinetic factors, especially deformation and fluids, in controlling reaction progress and how the resulting variability influences subsequent prograde history. The lack of a consistent metamorphic response, within and between adjacent schists, suggests that on both local and regional scales these rocks have largely not equilibrated at peak metamorphic conditions.     

Crystallization conditions of leucite-bearing magmas and their implications on the magmatological evolution of ultrapotassic magmas: the Vico Volcano, Central Italy

Summary Mineral compositions in leucite-bearing and leucite-free rocks from Vico volcano are reported. FeO/MgO partitioning (Kd_ol/liq) between olivine and latite (0.14–0.22), and between olivine and trachyte (0.06–0.10) indicates a lack of equilibrium between mineral and host rock. This suggests that mingling and/or mixing between magmas was a leading process during magmatic differentiation. In addition, a phono-tephrite olivine population with high (0.84) and equilibrium (0.23–0.29) Kd_ol/liq values has been produced by the interaction of differently evolved magmas. Zoning in clinopyroxene and plagioclase from these rocks recorded the same processes. In addition, resorbed quartz xenocrysts with coronas of clinopyroxene microlites indicate that digestion of crustal rocks occurred during the residence of magma in a shallow level reservoir. Increasing Fe coupled with decreasing Ca in diopside crystals from some phonolites, together with the petrographic and trace element data, indicate that polybaric fractional crystallisation also may be involved in the genesis of magmas of the second period of Vico activity. Leucite-free trachybasalts erupted in a late stage contain highly forsteritic olivine phenocrysts (forsterite 84–88 mol.%) in-equilibrium (Kd_ol/liq = 0.24–0.35) with the host rock, which indicate that they did not suffer chemical modification at low pressure. Received November 28, 2000; revised version accepted September 27, 2001     

初论铌、钽和钨的成矿作用：实验研究

针对目前没有关于Ｗ和Ｎｂ、Ｔａ的成矿作用与富氟钠长花岗岩成因关系的统一认识和实验证据的缺乏，我们完成了Ｗ、Ｎｂ、Ｔａ在流体和熔体中分配的一些实验。本研究旨在借助实验结果解释Ｗ、Ｎｂ、Ｔａ矿床的成因联系及它们成矿的可能机制。实验结果表明：在钠长石花岗岩熔体结晶过程中发生了Ｎｂ、Ｔａ和Ｗ的明显分离；钨倾向于在流体中分布，而Ｎｂ、Ｔａ则具有向硅酸盐熔体分配的趋势，在岩浆结晶晚期以独立矿物形式存在。这些实验结果与野外地质观察到的结果一致。     

The role of eclogites in the redistribution of water in the subcontinental mantle of the Siberian craton: results of determination of the water content in minerals from the Udachnaya pipe eclogites

A comprehensive study of 26 mafic mantle xenoliths from the Udachnaya kimberlite pipe was carried out. The contents of major and trace elements, equilibrium temperature parameters, and water content in the rock-forming minerals were determined. The temperatures of formation of the studied rocks are estimated at 800–1300 °C. According to IR spectroscopy data, the water content in clinopyroxenes from the studied eclogites varies from values below the detection limit to 99 ppm. The IR spectra of garnets lack bands of water. The water content in clinopyroxene and orthopyroxene from garnet websterite is 72 and 8 ppm, respectively. The water content in the average rock, calculated from the ratio of the rock-forming minerals, varies from a few to 55 ppm. No relationship among the water content, equilibrium temperatures, and rock composition is established. The low water contents in the eclogites are close to the earlier determined water contents in peridotites from the same pipe and are, most likely, due to the re-equilibration of the eclogites with the rocks of the peridotitic lithospheric mantle. The dehydration of the protolith during its subduction and the partial melting of eclogites before their removal by kimberlitic magma to the surface might be an additional cause of the low water contents in the mantle eclogite xenoliths.     

The Basil Cu–Co deposit,Eastern Arunta Region,Northern Territory,Australia: A metamorphosed volcanic-hosted massive sulphide deposit

The Basil Cu–Co deposit, Harts Range, central Australia, is hosted by the Riddock Amphibolite, a sequence that has been metamorphosed at upper-amphibolite- to granulite-facies conditions at 480–460 Ma (Larapinta Event), and subsequently reworked at amphibolite-facies conditions (450–300 Ma). As a result, many of the primary mineralization textures and other features that could characterise ore genesis have been obliterated. However, preserved textures and mineral relationships in the mineralized zone, allow some constraints to be placed on the genetic history of the deposit using mineralogical, petrographic and geochemical studies of host rocks and sulphides.Results of this study permit at least two genetic models to be ruled out. Firstly, whole rock geochemistry and garnet compositions suggest that the deposit is not a skarn system. Secondly, the lack of any significant Ni-signature, and the presence of abundant zircons in the host amphibolite (indicating that not all host rocks are mafic in composition and/or magmatic in character), make an orthomagmatic Ni–Cu–(PGE) system unlikely. Alternatively, Basil is assigned to a volcanic-hosted massive sulphide (VHMS)-style of mineralization, formed on the seafloor, within basaltic and sedimentary host rocks, typical of deposits occurring in such settings. The lack of a recognisable hydrothermal alteration zone is consistent with either destruction of the alteration zone during metamorphism or detachment of the ore from alteration during later deformation.The occurrence of sulphide inclusions within garnet and amphibole indicates that the sulphides must be syn-metamorphic or earlier. Partitioning of trace elements between pyrite and co-existing pyrrhotite suggests that (re)crystallization occurred under equilibrium conditions. The composition of sphalerite coexisting with pyrite and pyrrhotite indicates crystallization at pressures of at least 10 kbar, consistent with peak metamorphism during the Early Ordovician Larapinta Event. Zr-in-titanite geothermometry indicates peak temperatures of 730–745 °C.     

湖南金船塘锡铋矿床石榴子石原位LA-ICP-MS稀土元素分析及其意义

金船塘锡铋矿床是东坡矿田内一以锡铋为主的大型矽卡岩型多金属矿床。本文在详细野外地质考察、镜下观察以及电子探针分析的基础上,利用高精度LA-ICP-MS对该矿床的矽卡岩内石榴子石原位的微量元素进行了系统的分析。结果表明,金船塘锡铋矿床的钙铝榴石(Gro)大体上具重稀土(HREE)富集、轻稀土(LREE)亏损,负Eu异常的特征;而钙铁榴石(And)不同样品之间存在一定差异性,有的样品显示HREE富集、LREE亏损的特征,有的则轻重稀土分异不明显,除了多数呈Eu负异常外,还有部分表现为弱的正Eu异常,这可能是受钙铝-钙铁榴石混合物中的静电作用所导致。并且,上述不同石榴子石REE分配的差异还进一步指示,钙铝榴石(Gro)矿物生长速率较低,与孔隙流体之间基本保持动态平衡,水/岩(W/R)比值较低,其REE的化学行为主要受到晶体化学等机制的影响;钙铁榴石(And)矿物生长速率较高,具有较高的水/岩(W/R)比值,吸附作用在REE配分模式中起到重要作用。总体上,矽卡岩内的石榴子石的REE的分配呈HREE富集、LREE亏损,负Eu异常的特征,与千里山花岗岩REE分配模式一致,指示了金船塘锡铋矿床的成矿作用可能与千里山花岗岩体具有密切的成因联系。     

The Olivine--Orthopyroxene--Spinel Oxygen Geobarometer, the Nickel Precipitation Curve, and the Oxygen Fugacity of the Earth's Upper Mantle

The common upper mantle assemblage olivine-orthopyroxene-spinelmay be used to calculate the oxygen fugacity at which mantle-derivedperidotites have equilibrated. The equilibrium has been calibratedusing the large amount of existing data on the thermodynamicproperties of each phase in this assemblage. A by-product ofthis procedure is a new calibration of the olivine-spinel Mg-Fe²⁺exchange geothermometer. Application of the equilibrium to avariety of peridotite xenoliths indicates that the oxygen fugacityof the upper mantle lies between the quartz-fayalite-magnetite(QFM) and w?stite-magnetite (WM) oxygen buffers; the few apparentexceptions to this rule may be due to analytical error, particularlyin the Fe³⁺ content of the spinet phase. In fact, the determinationof Fe³⁺ in spinet is at present the limiting factor in the accurateapplication of the method: within this limitation, the presentlyavailable evidence suggests that the oxygen fugacity of themantle may be laterally homogeneous over wide regions, but mayalso show small differences between these regions. The fluidspecies in the system C-H-O at such oxygen fugacities are predominantlyCO₂ and/or H₂O, and not CH₄/H₂ The minimum possible oxygen fugacity of the mantle is givenby the nickel content of olivine in equilibrium with orthopyroxene;for typical mantle compositions this minimum curve is virtuallycoincident with the iron-w?stite (IW) oxygen buffer.     

全吸力范围南阳膨胀土的土-水特征曲线

膨胀土的失水收缩、吸水膨胀过程分别对应着土-水特征曲线的脱湿和吸湿阶段。土-水特征曲线对于研究非饱和土的水力与力学特性有着重要作用。用压力板法（吸力范围0～1.5 MPa）、滤纸法（吸力范围0～40 MPa）和蒸汽平衡法（吸力范围3～368 MPa）,分别对南阳膨胀土进行了土-水特性试验,得到全吸力范围内的土-水特征曲线。试验结果表明：初始孔隙比大致相同土样的土-水特征曲线,在低吸力范围内脱湿曲线与吸湿曲线具有明显的滞回现象。当吸力大于300 MPa时,土-水特征曲线的滞回效应基本消失,即脱湿曲线与吸湿曲线基本重合。滤纸法所测出的土-水特性落在主脱湿和主吸湿曲线的滞回圈内。当吸力等于367.54 MPa时,含水率仅为0.325%,几乎近于0。孔隙比随着吸力的变化规律中,不仅受到吸力大小的影响,还受到吸力历史和吸力路径影响;孔隙比与吸力关系中,相同吸力时吸湿路径的孔隙比要比脱湿路径的大;在吸力低范围,吸湿路径与脱湿路径的孔隙比相近。孔隙比与饱和度关系因吸力路径的不同也存在着明显的滞回效应,接近饱和时趋近一致。变吸力情况条件下,饱和度随着孔隙比的增加而增加,蒸汽平衡法得出的孔隙比与饱和度的关系具有明显的线性关系,而压力板法做出来的低吸力范围内的线性关系不明显。     

Oxygen isotope studies of the geothermal system at Wairakei,New Zealand

Volcanic rocks in the Wairakei geothermal field have undergone extensive oxygen isotope exchange with the thermal waters, resulting in an O¹⁸-depletion averaging about 4%. A lower limit on the ratio of the mass of water to rock in the exchange system is 4·3, at least ten times greater than the corresponding figure for the Salton Sea geothermal system. Carbonates, present as alteration products in most samples, are found to be in equilibrium with waters at present-day temperatures in some wells, and to record higher ‘fossil’ temperatures in others. Quartz phenocrysts and xenocrysts remain unexchanged, and only new hydrothermal quartz is in isotopic equilibrium with geothermal solutions.