青铜文物腐蚀过程中的次生矿物

产于不同环境不同地方的青铜文物经矿相显微镜观察、电子探针成分分析和X射线衍射研究表明，在青铜文物腐蚀层中观察到次生矿物——赤铜矿、孔雀石、蓝铜矿、白铅矿和锡石。由上述矿物组成的腐蚀层在青铜器表面形成保护层。腐蚀层细分为红色赤铜矿层、绿色碳酸盐矿物层和黄色锡石层组成，其厚度小于1mm。青铜合金在潮湿条件下的腐蚀比在干旱条件下要严重，另外青铜合金是适用于作高放废物地质处置系统中的废物罐的候选材质。     

碳酸岩Sr、Nd、Pb 同位素地球化学研究评述

碳酸岩是出露相对较少的幔源岩石，其中Sr与Nd是研究地幔物质组成的主要对象之一。本文统计了世界上主要碳酸岩的锶、钕、铅同位素组成特征；研究显示，碳酸岩源区主要是洋岛玄武岩高U／Pb的HIMU端员和富集端员(EM1或EM2)的混合作用；此外大部分碳酸岩的锶、钕同位素落在大洋玄武岩范围内；这些均表明其成因与地慢柱有密切联系。碳酸岩及与之共生的硅酸岩的同源或独立源区模式部很难充分解释两者同位素组成特征，逭反映碳酸岩的演化模式涉及更复杂的过程。可能是俯冲作用使碳酸岩源区经历不同时间和程度的富集、亏损过程导致地幔源区成分不均一。     

P–T–fO2 controls on a partly inverse chromite-bearing ultramafic intrusive: an evaluation from the Sukinda Massif, India

The chromites from the alpine type ultramafic intrusive of Sukinda, India, display a typical partly inverse spinel form and occur in two distinct zones: Brown Ore Zone (BOZ) and Grey Ore Zone (GOZ). The host ultramafites are mostly altered and are represented by the serpentinite, tremolite-talc(chlorite) schist, talc-serpentine schist and chlorite rock. The less altered variants are dunite, harzburgite and websterite. A dyke of orthopyroxenite runs through the main ultramafic body.The composition of olivine (Fo₉₂), orthopyroxene (En_92–89) and Al₂O₃ contents of the parental liquid (10.40–11.45%) determined from chromites, suggest that the parent melt is of boninitic affinity. The chemical plot of TiO₂ content against cr# of chromites corroborates a boninitic parental melt. The Fe–Mg partitioning in olivine and chromite depicts the temperature for chromitites as 1200 °C. A compositional plot of mg# and cr# suggests crystallization at high pressure conditions, corresponding to the kimberlite xenolith field. From the P–T diagram of pyrolite melting and mineral assemblage, the pressure of crystallization is stipulated to be ≥1.2 GPa. The f_O2 values estimated from Fe³⁺/Cr+Al+Fe³⁺ ratios range from 10^−8.3 to 10^−9.3 for the GOZ and 10^−7.1 to 10^−7.3 for the BOZ. The f_O2 values together with the pressure range suggest crystallization at upper mantle conditions. The heterogeneity in chemical composition and f_O2 conditions for the GOZ and BOZ could be linked to heterogeneity in the upper mantle.     

Mantle Xenoliths from the Southeastern Slave Craton: Evidence for Chemical Zonation in a Thick, Cold Lithosphere

We present the first data on the petrology of the mantle lithosphereof the Southeastern (SE) Slave craton, Canada. These are basedon petrographic, mineralogical and geochemical studies of mantlexenoliths in Pipe 5034 of the Cambrian Gahcho Kué kimberlitecluster. Major types of mantle xenoliths include altered eclogite,coarse garnet or spinel peridotite, and deformed garnet peridotite.The peridotites belong to the low-temperature suite and formedat T=600–1300°C and P= 25–80 kbar in a thick(at least 220–250 km), cool lithosphere. The SE Slavemantle is cooler than the mantle of other Archaean cratons andthat below other terranes of the Slave craton. The thick lithosphereand the relatively cool thermal regime provide favourable conditionsfor formation and preservation of diamonds beneath the SE Slaveterrane. Similar to average Archaean mantle worldwide, the SESlave peridotite is depleted in magmaphile major elements andcontains olivine with forsterite content of 91–93·5.With respect to olivine composition and mode, all terranes ofthe Slave mantle show broadly similar compositions and are relativelyorthopyroxene-poor compared with those of the Kaapvaal and Siberiancratons. The SE Slave spinel peridotite is poorer in Al, Caand Fe, and richer in Mg than deeper garnet peridotite. Thegreater chemical depletion of the shallow upper mantle is typicalof all terranes of the Slave craton and may be common for thesubcontinental lithospheric peridotitic mantle in general. Peridotiticxenoliths of the SE Slave craton were impregnated by kimberliticfluids that caused late-stage recrystallization of primary clinopyroxene,spinel, olivine and spinel-facies orthopyroxene, and formationof interstitial clinopyroxene. This kimberlite-related recrystallizationdepleted primary pyroxenes and spinel in Al. The kimberliticfluid was oxidizing, Ti-, Fe- and K-rich, and Na-poor, and introducedserpentine, chlorite, phlogopite and spinel into peridotitesat P < 35 kbar. KEY WORDS: kimberlite xenolith; lithosphere; mantle terrane; chemical zoning; thermobarometry; Slave craton     

Mafic Pegmatites Intruding Oceanic Plateau Gabbros and Ultramafic Cumulates from Bolivar, Colombia: Evidence for a 'Wet' Mantle Plume?

The fault-bounded Bolívar Ultramafic Complex (BUC) onthe eastern fringes of the Western Cordillera of Colombia wastectonically accreted onto the western coast of South Americain the late Cretaceous–early Tertiary, along with pillowbasalts of the Caribbean–Colombian Oceanic Plateau (CCOP).The complex consists of a lower sequence of ultramafic cumulates,successively overlain by layered and isotropic gabbroic rocks.The gabbros grade into, and are intruded by, mafic pegmatitesthat consist of large magnesiohornblende and plagioclase crystals.These pegmatites yield a weighted mean ⁴⁰Ar–³⁹Ar step-heatingage of 90·5 ± 0·9 Ma and thus coincidewith the timing of peak CCOP volcanism. The chemistry of theBUC is not consistent with a subduction-related origin. However,the similarity in Sr–Nd–Pb–Hf isotopes betweenthe CCOP and the BUC, in conjunction with their indistinguishableages, suggests that the BUC is an integral part of the plume-derivedCCOP. The parental magmas of the Bolívar complex wereprobably hydrous picrites that underwent 20–30% crystallization.The residual magmas from this fractionation contained     

A method for calculating effective bulk composition modification due to crystal fractionation in garnet-bearing schist: implications for isopleth thermobarometry

Quantitative P–T path determination in metamorphic rocks is commonly based on the variation in composition of growth‐zoned garnet. However, some component of growth zoning in garnet is necessarily the result of an effective bulk composition change within the rock that has been generated by crystal fractionation of components into the core of garnet. Therefore, any quantitative calculation of the P–T regime of garnet growth should be completed using an accurate assessment of the composition of the chemical system from which garnet is growing. Consequently, a method for calculating the extent of crystal fractionation that provides a means of estimating the composition of the unfractionated rock at any stage during garnet growth is developed. The method presented here applies a Rayleigh fractionation model based on measured Mn content of garnet to generate composition v. modal proportion curves for garnet, and uses those curves to estimate the vectors of crystal fractionation. The technique is tested by calculating the precision of the equilibrium between three garnet compositional variables within the chemical system determined to be appropriate for each of a series of microprobe analyses from garnet. Application of the fractionation calculations in conjunction with the P–T estimates based on intersecting compositional isopleths provides a means of calculating P–T conditions of garnet growth that is based on individual point‐analyses on a garnet grain. Such spatially precise and easily obtainable P–T data allow for detailed parallel studies of the microstructural, the P–T, and the chemical evolution of metamorphosed pelites. This method provides a means of studying the dynamics of orogenic systems at a resolution that was previously unattainable.     

“Three-Component” Digital Prospecting Method：A New Approach for Mineral Resources Quantitative Prediction and Assessment

“Three-component” method consists of three clase-connected aspects: geological anomaly,diversity of mineralization and mineral deposit spectrum. All these three concepts are not new separately, but it is a new approach to combine these three aspects in one single concept for quantitative mineral resources prediction and assessment and it is also the first time to conduct a more detailed study in each aspect. Investigation and clarification of geological anomalies, diversity of mineralization and spectrum of mineral deposits are realized by digitization and quantification of ore forming controlling factors, oreexisting symbols or marks, characteristics of mineralization and regulation of ore-genesis and laws of distribution. These procedures lead to construction of a “digital model“ for mineral resources prediction andassessment.     

Statewide Estimates of Undiscovered Deposits of Gold,Silver, Copper,Lead, and Zinc

Estimates of the number of undiscovered deposits on a statewide basis offer a different perspective on the nation's undiscovered resources of gold, silver, copper, lead, and zinc. Mean estimates of the number of undiscovered deposits statewide were extracted from the estimates of undiscovered deposits nationwide. More than 50 undiscovered deposits are estimated to occur in Alaska, Arizona, Nevada, and Wisconsin. Estimating the number of undiscovered deposits statewide serves as a measure of a state's total remaining mineral resources in known conventional deposit types.