Granite-hosted gold mineralization at Timbarra, northern New South Wales, Australia

The Timbarra gold deposits, located in the southern New England Fold Belt of New South Wales, Australia, represent an economically significant and distinctive member of the intrusion-related class of gold deposits. The five known deposits possess a total identified mineral resource of 16.8 Mt at 0.73 g/t gold, for a total of 396,800 contained ounces. The granites in the Timbarra region form a texturally complex, zoned pluton. The gold deposits are found within the Stanthorpe leucomonzogranite (242 to 238 Ma), which intrudes and forms a core to the more mafic, barren, Bungulla monzogranite (248 to 243 Ma). Gold is disseminated in the roof zone (upper 240 m) of a fractionated, magnetite- and ilmenite-bearing, I-type leucomonzogranite phase of the Stanthorpe body. The entire gold resource occurs in the areally extensive main leucomonzogranite pluton and is hosted by a medium- to coarse-grained granite. Disseminated ore is present in all five deposits, comprises >95% of the overall resource at Timbarra, and occurs predominantly as gently dipping, tabular to lenticular bodies that are conformably constrained beneath a fine-grained aplite carapace and internal aplite layers. The disseminated ore consists of gold-bearing muscovite-chlorite-carbonate alteration and infill of primary miarolitic cavities within massive leucomonzogranite or microgranite, and contains no discernable vein, joint, or fracture control at the outcrop or hand specimen scale. Structurally controlled mineralization forms the remaining 5% of the Timbarra resource, and comprises minor, low-density (0.02 to 0.25 per meter), vein-dikes and quartz-molybdenite veins emplaced along steeply dipping east-southeast, east-northeast, and north-northeast striking cooling joints. Both mineralization styles and alteration share a common paragenetic sequence of mineral precipitation. Quartz, perthitic K-feldspar, minor biotite, and albite are the earliest and most abundant infill minerals and commonly line primary cavities and vein-dikes. Subsequent minerals include coeval arsenopyrite, pyrite, fluorite, and molybdenite. The latest minerals include muscovite, chlorite, gold, calcite, silver-bismuth telluride, lead-bismuth telluride, and rare galena and chalcopyrite. The gold ore has a low total sulfide mineral concentration (Б%). Ore contains elevated concentrations of Bi, Ag, Te, As, Mo, and Sb; gold is strongly correlated with Bi, Ag, and Te, but only weakly with Mo, As, and Sb. Gold grains are generally <1 to 50 µm in size, but rarer grains as large as 1 mm in diameter have been observed. Gold fineness ranges from 950 to 600, and varies both within and between individual grains for a given deposit. The moderately oxidized I-type host granite, low-sulfide (Б%) ores, Au-Bi-Ag-Te geochemical signature, muscovite-chlorite-carbonate alteration assemblage, and low-salinity aqueous and carbonic fluids suggest that Timbarra is part of the newly recognized intrusion-related gold deposit class. Timbarra is distinguished from other intrusion-related gold deposits by the disseminated mineralization style within pervasively altered granite, forming gently dipping, tabular to lenticular ore zones.     

Application of CCSEM to heavy mineral deposits: Source of high-Ti ilmenite sand deposits of South Kerala beaches, SW India

For the characterization of sediments, Computer Controlled Scanning Electron Microscopy (CCSEM) is a powerful method in obtaining chemical data on individual mineral grains and modal analysis of the heavy mineral fraction of sediment samples. Here we show how the CCSEM method can be used to evaluate ilmenite ore grade as well as a tool to investigate the source of heavy mineral deposits.The heavy mineral rich deposits in beach sands around the town of Chavara in SW India are characterized by ilmenite with elevated TiO₂ contents, often exceeding 60 wt.%. In order to determine the origin of these high-TiO₂ ilmenite deposits, we collected a series of beach sediment samples (22) from a c. 800 km long stretch of coastline from northern Kerala state to well within the Tamil Nadu state. A set (7) of river sediments was also taken, roughly covering the catchment area to the beach samples. The data show that the sediments in the Chavara high-Ti ilmenite deposit are distinguished by minor elements in ilmenite, garnet chemistry and heavy mineral assemblage: Chavara ilmenite has high MgO and low MnO contents; garnets have low grossular components and the heavy mineral assemblage is dominated by sillimanite–kyanite in addition to ilmenite. These features correlate with basement geology in the hinterland, and with sediments from rivers, draining the basement. Based on these observations we conclude that high-Ti ilmenite from Chavara beaches originates in the khondalite belt of high-grade metasediments. Our study demonstrates rapid mineral analyses in sediments by CCSEM to be efficient in the characterization of mineral compositions and assemblages in sediments, in the identification of possible source regions and thus ultimately in exploration for industrial mineral resources.     

The partitioning of trace transition elements in crystal structures: a provocative review with applications to mantle geochemistry

Interrelationships between chemical compositions and crystal structures of minerals pioneered by Goldschmidt have been overlooked by modern geochemists. While analytical techniques and data for trace elements have become more sophisticated, progress has been slow in relating abundance data of individual elements to their relative enrichments in specific sites in mineral structures. The concept of diadochy has degenerated into an analytical relationship between major and trace elements, instead of its original crystallographic basis of replacement of one atom by another at a specific site in a crystal structure. Future interpretations of trace element data must consider the partitioning of atoms between different coordination sites in multisite mineral structures.The well-known partitioning of nickel and chromium into the earliest minerals during magmatic crystallization is extended to magma evolution in the mantle. The strong preference of Ni²⁺ and Cr³⁺ for octahedral sites in minerals leads to their enrichment in certain Iherzolites which are refractory residua during partial fusion of the mantle.     

NEW SET OF LOW CONCENTRATION STANDARDS FOR LA, CE, SM, YB, LU, Y, SC, V, NB AND TA IN SILICATES

We have developed a set of four synthetic standards for the rare earth and high field strength elements designed for use in the determination of those elements in silicates. The base material is a glass nominally at the eutectic of the MgO-Al₂O₃-SiO₂ ternary system. The nominal doping level was 2 wt% of the elements as oxides. To avoid problems associated with peak interference, the elements were doped in four separate glasses.     

Geochemical controls on a calcite precipitating spring

A small spring fed stream was found to precipitate calcite by mainly inorganic processes and in a nonuniform manner. The spring water originated by rainwater falling in a 0.8 km² basin, infiltrating, and dissolving calcite and dolomite followed by dissolution of gypsum or anhydrite. The Ca²⁺/Mg²⁺ indicates that calcite is probably precipitated in the subsurface from a supersaturated solution. This water emerges from the spring still about 5 times supersaturated with respect to calcite and continues calcite precipitation. When 10 times supersaturation is reached, due to CO₂ degassing the precipitation is more rapid. The calcite accumulation from the stream with a flow of 5 l/s is calculated to be 12600 kg/yr with the highest rates in areas where CO₂ degassing is the greatest. The non-equilibrium, as shown by the high calcite supersaturation, is also reflected in a variable partitioning pattern for Sr²⁺ between the water and calcite.     

Petrological and trace element geochemical features of the Okete Volcanics,western North Island,New Zealand

The Okete Volcanics form small volume monogenetic volcanoes situated around the flanks of larger tholeiitic cones of the Plio-Pleistocene Alexandra Volcanics, in the back-arc tectonic environment of western North Island, New Zealand. The lavas and tuffs of the Okete Volcanics have compositions which include basanites, alkali olivine basalts, olivine tholeiites, and hawaiites. Most rocks have Mg numbers >66, >250 p.p.m. Ni, >500 p.p.m. Cr, and often contain ultramafic xenoliths, which indicate that they are very close to being primary magmas. The Okete Volcanics show geochemical trends, from basanite to hawaiite, of progressive depletion of both compatible and incompatible trace elements, progressive increase in Al₂O₃, and heavy REE and Y enrichment with crossingover REE patterns in the hawaiites. These geochemical trends can be accounted for by varying degrees of partial melting of a light REE enriched garnet peridotite with subsequent modification of the melts near source or during ascent by fractional crystallization of olivine and minor clinopyroxene. Mass balance calculations cannot quantitatively constrain the degree of partial melting or fractional crystallization, but nevertheless indicate that the Okete alkali olivine basalts, olivine tholeiites, and hawaiites have been derived by successively larger degrees of partial melting relative to basanites, and have also been progressively more modified by fractional crystallization than have the basanites. Sources of the alkalic melts lay at depths corresponding to >20 kb, and most of the ultramafic xenoliths, apart from some which may be cognate cumulates, are unrelated to the magmas that brought them to the surface. Magmas have changed in composition with time from older smaller-volume volcanoes of basanite or alkali olivine basalt compositions, to younger and more voluminous volcanoes which contain hawaiites. The geochemical trends shown by the Okete Volcanics and their spatial association with voluminous tholeiitic volcanism, are features which are different from those observed elsewhere in the Pliocene to Recent basaltic fields of northern North Island, and may be related to their unique tectonic setting, situated in a distinct structural domain.     

Experimental studies At 5–12 GPa of the Ondermatjie hypabyssal kimberlite

Liquidus and sub-liquidus phase relationships are reported for melts formed from an aphanitic kimberlite composition crystallized at 5–12 GPa and 900–1400 °C. The liquidus phase over the pressure range investigated is forsteritic olivine. This is followed with decreasing temperature by olivine plus garnet as the initial sub-liquidus solid phase assemblage. Supra-solidus assemblages consist of olivine+garnet+clinopyroxene+Mg-ilmenite+liquid at 5–7 GPa or olivine+garnet+clinopyroxene+hematite–ilmenite solid solutions (+/−perovskite)+liquid at 8–12 GPa. Phlogopite forms as a near-solidus phase only at 900 °C and 6 GPa. Orthopyroxene does not form at any temperature and pressure. All garnets formed at 6–7 GPa are Ti-rich almandine–grossular–pyrope solid solutions and not Cr-pyrope, whereas garnets formed above 8 GPa are Ti- and Fe³⁺-rich and have no natural counterparts. Quenched liquids are represented by magnesite at 10–12 GPa and Mg–Ca-carbonates at lower pressures. In addition to forming discrete crystals, Mg-ilmenite and hematite–ilmenite solid solutions occur as lamellar intergrowths that are identical in texture to naturally occurring intergrowths. Mg-ilmenite compositions at 6–7 GPa are similar to those of the natural occurrences, whereas clinopyroxenes are richer in Ca. The effects of graphite versus platinum capsules on the oxygen fugacity of the experimental charges and the composition of the olivine, clinopyroxene, Fe–Ti-oxides and garnets formed are described. These experimental data are interpreted to indicate that kimberlite magmas are unlikely to be formed by very small degrees of partial melting of a simple homogeneous carbonated garnet lherzolite mantle. It is proposed that kimberlite magmas form by extensive partial melting of metasomatized mantle, i.e. mineralogically complex carbonate-bearing veins in a lherzolitic/harzburgitic substrate, and that lamellar ilmenite–clinopyroxene intergrowths represent the products of non-equilibrium growth in kimberlite magma.     

Measurements of coupled fluid and sediment motion over mobile sand dunes in a laboratory flume

The relationship between turbulent fluid motions and sediment particle motions over mobile sand dunes was investigated by using a laser Doppler velocimeter and an acoustic backscatter system in laboratory experiments performed at the USDA-ARS-National Sedimentation Laboratory. Profiles of acoustic backscatter from particles and at-a-point turbulence data were collected while translating both measurement devices downstream at the speed of mobile dune bedforms. The resulting data set was used to examine the frequency （recurrence frequency） at which the fluctuating backscatter and fluid velocity signals exceeded magnitude thresholds based on the standard deviation （σ） of the local velocity and the magnitude the acoustic signal resulting from backscatter from suspended particles. The slope of the downstream and vertical velocity recurrence frequencies generally indicated a gradually increasing recurrence time with increasing elevation. The recurrence frequency for acoustic backscatter data was not strongly variable with elevation. The closest correspondence between the recurrence frequencies of sediment backscatter and vertical velocities at the 1σ magnitude threshold was in a region defined by X/L〈0.4 and y〈6 cm. The downstream velocity was most closely related to backscatter in a small region at 0.4〈X/L〈0.8 and less than 3-4 cm from the bed.     

中国大中城市流动人口迁移规律研究

本文在对西方国家人口流动研究进行综述的基础上,通过北京,天津,南京,廓坊,唐山和昆山等大中城市流动人口问卷调查,首次对大中城市流动人口迁移和流动特征,从业结构,迁移原因与途径进行了系统的研究。中国现在正在经历大规模的农村流动人口向城市迁移的过程。     

Three-Dimensional Scalar Microfront Systems in a Large-Eddy Simulation of Vegetation Canopy Flow

Large-eddy simulation is used to reproduce neutrallystratified airflow inside and immediately above a vegetation canopy. A passive scalaris released from the canopy and the evolution of scalar concentration above the canopyis studied. The most significant characteristic of the scalar concentration is the repeatedformation and dissipation of scalar microfronts, a phenomenon that has been observedin nature. These scalar microfronts consist of downstream-tilted regions of highscalar concentration gradients. Computer visualization tools and a conditional samplingand compositing technique are utilized to analyze these microfronts. Peaks in positivepressure perturbation exceeding an experimental threshold are found to be effectiveindicators of scalar microfronts. Convergence of the streamwise velocity componentand divergence of the cross-stream velocity component are observed in the immediatevicinity of scalar microfronts, which helps explain their relatively longlifetimes. Many of these three-dimensional features have been observedin previous field studies of canopy flow.