地气法－找深部金矿的新方法

介绍一种八十年代发展起来的找深部金矿的新方法一地气法。文中讨论了地气法的找矿机理，认为是地壳中上升气流将成矿元素微粒携带至地表而造成多元素异常。对工作方法着重讨论了地气采样与测试的系统，以及比较了积累式取样的效果。最后列出山东招远地区大尹格庄金矿８０号勘探线的地气测量多元素异常图。     

Green synthesis of magnetic mesoporous silica nanocomposite and its adsorptive performance against organochlorine pesticides

Green synthesis of nanomaterials has received increasing attention as an eco-friendly technology in materials science. Here, we have used two types of extractions from green tea leaf (i.e., total extraction and tannin extraction) as reducing agents for a rapid, simple and one-step synthesis method of mesoporous silica nanoparticles/iron oxide nanocomposite based on deposition of iron oxide onto mesoporous silica nanoparticles. Mesoporous silica nanoparticles/iron oxide nanocomposite were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, energy-dispersive X-ray, vibrating sample magnetometer, N₂ adsorption and high-resolution transmission electron microscopy. Mesoporous silica nanoparticles/iron oxide nanocomposite was used as a solid adsorbent for removal of lindane pesticide from aqueous solutions. The developed system possesses the advantages of silica as core that include large surface area and advantages of iron oxide (shell) that include the capability to interact with chlorinated compounds and ability to release by using external magnetic field. UV-Vis technique was used as a simple and easy method for monitoring the removal of lindane. Effects of pH and temperature on the removal efficiency of the developed mesoporous silica nanoparticles/iron oxide nanocomposite toward lindane pesticide were also investigated. Fourier transform infrared spectroscopy, high-performance liquid chromatography and gas chromatography techniques were used to confirm the high ability of mesoporous silica nanoparticles/iron oxide nanocomposite for sensing and the capture of lindane molecules with high sorption capacity (about 99%) that could develop a new eco-friendly strategy for detection and removal of pesticide and as a promising material for water treatment.     

Quaternary Antarctic Bottom-Water history: Deep-sea benthonic foraminiferal evidence from the southeast Indian Ocean

Distinct assemblages of Recent deep-sea benthonic foraminifera from the southeast Indian Ocean have been shown to be associated with Antarctic Bottom Water (AABW) and Indian Bottom Water (IBW). The AABW assemblage is divided into two groups. One is dominated by Epistominella umbonifera and is associated with AABW having temperatures between ?0.2° and 0.4°C. The second group is dominated by Globocassidulina subglobosa and is associated with AABW having temperatures between 0.6° and 0.8°C. The IBW assemblage is marked by the strong dominance of Uvigerina spp. and Epistominella exigua. The faunal-water-mass relationships have been used to infer the history of bottom-water circulation over the last 500,000 yr in this region using faunal data from four Eltanin cores. One core was taken from the Southeast Indian Ridge in association with IBW, and three were taken from the flank of the ridge associated with AABW flowing within a western boundary contour current in the South Australian Basin. Little faunal variation exists in the core beneath IBW (E48-22), indicating that IBW was present on the Southeast Indian Ridge during the last 300,000 yr. A record of the intensity of AABW circulation during the last 500,000 yr is inferred from the benthonic foraminiferal data in the three cores located within the western boundary contour current. Marked oscillations in the relative proportions of AABW and IBW faunal assemblages are found in one core, E48-03. The faunal variations are inferred to have resulted from variation in intensity of AABW circulation between 500,000 and 195,000 yr B.P. In E48-03, the AABW assemblage was present most of the time between 500,000 and 195,000 yr B.P., with low intensity of AABW circulation occurring primarily during the equivalent of stages 8 and 7 (t = 305,000 to 195,000 yr B.P.). The intensity of AABW circulation varied, with a maximum occurring during the equivalent of stage 11 (t = 420,000 yr B.P.). Two additional cores, E45-27 and E45–74, show relatively constant intensity of AABW circulation from 195,000 yr B.P. to the present. The intensity of AABW circulation at the present appears to be intermediate between a maximum during the equivalent of stage 11 (t = 420,000 yr B.P.) and the minimum during the equivalent of stage 8 (t = 275,000 yr B.P.). AABW production has occurred during both glacial and interglacial episodes. Bottom-water productivity has been suggested to play an important role in glacial/interglacial oscillations during the late Quaternary (Weyl, 1968; Newell, 1974). In this study, the relationship between bottom-water circulation and climatic fluctuations appears to be more complex than had been previously suggested, since a simple relationship between Quaternary bottom-water circulation and paleoclimatic fluctuations is not shown.     

Phase relations of pyroxene and amphibole in greenstone,blueschist and eclogite of the Franciscan Complex,California

The phase relations of pyroxenes, amphiboles and associated minerals in metamorphic rocks of the Franciscan Complex can be graphically depicted on a ternary diagram which has at its apices the metamorphic clinopyroxene end members, viz NaAl-NaFe³⁺-Ca(Fe²⁺, Mg). Phases are plotted by projection from a constant subassemblage of minerals. This analysis allows interpretation of the effects of pressure, temperature, bulk rock composition and fluid composition on stability of minerals within the Franciscan.Pyroxenes in meta-igneous rocks and metagraywackes have a limited compositional range and fall into two groups: the omphacites, with 50±5% diopside +hedenbergite component; and the jadeitic pyroxenes with 10±5% diopside+hedenbergite. Pyroxenes intermediate between these two groups are unstable relative to assemblages containing Na-amphibole+other minerals.Coexisting pyroxenes and amphiboles in eclogites and associated coarse blueschists comprise equilibrium assemblages, and the proportion of pyroxene to amphibole is a function of rock composition. Eclogites are stable at higher temperature than regionally developed fine-grained greenstones and blueschists in the Franciscan, and at higher pressure than amphibolites. X _H2O ^fluid is not an important factor in the stability of Franciscan eclogite relative to amphibolite.     

Petrogenesis and chronology of lunar meteorite Northwest Africa 4472: A KREEPy regolith breccia from the Moon

Northwest Africa (NWA) 4472 is a polymict lunar regolith meteorite. The sample is KREEP-rich (high concentrations of potassium, rare earth elements and phosphorus) and comprises a heterogeneous array of lithic and mineral fragments. These clasts and mineral fragments were sourced from a range of lunar rock types including the lunar High Magnesian Suite, the High Alkali Suite, KREEP basalts, mare basalts and a variety of impact crater environments. The KREEP-rich nature of NWA 4472 indicates that the sample was ejected from regolith on the nearside of the Moon in the Procellarum KREEP Terrane and we have used Lunar Prospector gamma-ray remote sensing data to show that the meteorite is most similar to (and most likely sourced from) regoliths adjacent to the Imbrium impact basin.U-Pb and Pb-Pb age dates of NWA 4472 phosphate phases reveal that the breccia has sampled Pre-Nectarian (4.35 Ga) rocks related to early episodes of KREEP driven magmatism. Some younger phosphate U-Pb and Pb-Pb age dates are likely indicative of impact resetting events at 3.9-4 Ga, consistent with the suggested timing of basin formation on the Moon. Our study also shows that NWA 4472 has sampled impact melts and glass with an alkali-depleted, incompatible trace element-rich (high Sc, low Rb/Th ratios, low K) compositional signature not related to typical Apollo high-K KREEP, or that sampled by KREEPy lunar meteorite Sayh al Uhaymir (SaU) 169. This provides evidence that there are numerous sources of KREEP-rich protoliths on the Moon.     

The Late Cretaceous Impact of the Trindade Mantle Plume: Evidence from Large-volume, Mafic, Potassic Magmatism in SE Brazil

When the subcontinental lithospheric mantle undergoes heatingand/or extension, some of the earliest mafic melts to be generatedare those rich in volatUes and potassium. In some cases, e.g.when a plume impinges on thick cratonic lithosphere or whenthe amount of extension is very small, K-rich mafic igneousrocks may be the only surface expression of mantle melting.The Alto Paranaiba Igneous Province, in SE Brazil, is one ofthe world's most voluminous mafic potassic provinces (>15000km³),which until recently was relatively unknown. The magmas wereemplaced into a narrow Proterozoic mobile belt close to thesurface margin of the Sao Francisco craton, and it is one ofseveral Cretaceous alkaline igneous provinces that are locatedaround the margin of the Parana sedimentary basin in Braziland Paraguay.Detailed geochemical analyses of samples from throughoutthe Alto Paranaiba Igneous Province show that it is composedof a relatively diverse suite of ultrapotassic-potassic, ultramaficmqfic,silica-undersaturated lavas and hypabyssal intrusions, i.e.kimberlites, madupitic olivine lamproites and kamafugitic rocks.These all have very high concentrations of incompatible traceelements and are all strongly enriched in light rare earth relativeto heavy rare earth elements (e.g. La/Yb=50-230). Wide variationsin major element ratios, which are unrelated to the effectsof crystal fractionation in these magmas (e.g. CaO/Al₂O₃), suggestthat the mafic potassic rocks were derived from a heterogeneousmantle source. They show relatively restricted ranges of initial⁸⁷Sr/⁸⁶Sr (070436-070588) and Nd₂₅ values of -4 to -8, intermediatebetween Group I and II South African kimberlites. T_DM Nd isotopemodel ages of 900 Ma suggest that the magmas were derived bythe remobilization of subcontinental lithospheric mantle thathad been enriched by small-volume K-rich melt fractions sincethe Late Proterozoic.New K/Ar ages for mica separates show thatthe kimberlites, madupitic olivine lamproites and kamafugiticrocks were emplaced together with large carbonatite-bearingplutonic complexes at 85 Ma. Reconstructions of plate motionsshow that, at this time, the location of the Alto ParanaibaIgneous Province coincided with the postulated position of thepresent-day Trindade(or Martin Vaz) plume. We propose that thewidespread Late Cretaceous alkaline magmatism in SE Brazil mayhave been caused by impingement of this plume on the base ofthe subcontinental lithosphere. Heat penetrating the lithosphere,both by conduction and advection by asthenospheric-source decompressionmelts, may have caused melting of the readily fusible partsof the lithospheric mantle and the genesis of mafic potassicand (after fractionation) carbonatite magmas. The Proterozoicmobile belt (the Brasilia Belt) appears to have acted as a Hhinspofrelative to the adjacent Sao Francisco craton, allowing greaterupwelling and melting of the asthenosphere. Subsequently, asthe craton passed over the plume, volcanism was switched off'until the Early Tertiary when the plume reemerged from beneaththe westward drifting South America continent and was the magmasource for oceanic-islands and seamounts of the Trindade-Vitriachain. Corresponding author     

Importance of heavy metal-organic matter interactions in natural waters

The role of organic ligands in metal complexing in natural waters has received little attention because of uncertainties regarding both the abundance and nature of dissolved organic carbon compounds. Recent data show that the bulk of dissolved organic matter in natural waters consists of highly oxidized and chemically and biologically stable polymeric compounds closely resembling soil humic substances. Average molar concentrations of these aquatic humics in major U.S. rivers range from 5 × 10^?6to 3 × 10^?5 moles 1^?1. Fractional elution of soil organic matter by meteoric waters may be considered to be the main process contributing to the presence of humic matter in rivers. The aquatic humic polymers participate in complex formation through ionizable functional groups with a range of differential acidities. The stabilities of metal-humic complexes in natural waters are higher than those of the corresponding inorganic metal complexes. Quantitative evaluation of the metal-organic interactions can be approached by applying variable equilibrium functions which take into account the differential physico-chemical characteristics of the active complexing sites on the polymer molecule. Assuming an average humic concentration of 10 mg 1^?1, complexation of trace metals can be significant even in the presence of excess concentrations of major cations.     

Effect of nano-hematite morphology on photocatalytic activity

Nano-hematites, i.e., hematites with nanoparticle-, nanorod-, and nanotube-like morphologies, were synthesized via the hydrothermal method by controlling the reaction time, temperature, and reactant concentration. The nano-hematites of different crystal shapes all exhibited band gaps within the visible-light region (1.56–2.1 eV). Further, they showed weak ferromagnetic behavior, and their coercive magnetic field was larger than that of the bulk hematite. Moreover, all the nano-hematites also exhibited high photocatalytic activities during the degradation of methylene blue under visible-light irradiation. The experimental data fitted the Langmuir–Hinshelwood kinetics model very well. The nanorods had the highest photocatalytic rate constant per unit surface area, possibly owing to a higher aspect ratios; this lowers the electron–hole recombination rate. These results suggest that the crystal morphology of hematites has a significant effect on their physical and photocatalytic properties. Therefore, controlling the morphology of the materials is essential for obtaining well-tailored photocatalysts.     

An infrared spectroscopic study of lawsonite to 20 GPa

The infrared spectrum of CaAl₂Si₂O₇ · H₂O-lawsonite, has been characterized to pressures of 20 GPa at 300 K. Our results constrain the response to compression of the silicate tetrahedra, hydroxyl units, and water molecules in this material. The asymmetric and symmetric stretching and bending vibrations of the Si₂O₇ groups (at zero pressure frequencies between 600 and 1000 cm⁻¹) increase in frequency with pressure at rates between 3.6 and 5.9 cm⁻¹/GPa. All silicate modes appear to shift continuously with pressure to 20 GPa, although the lowest frequency stretching vibration becomes unresolvable above 18 GPa, and a splitting of the main bending vibration is observed near this pressure. The O-H stretches of the hydroxyl units exhibit a discontinuity in their mode shifts at ∼8–9 GPa, which we interpret to be produced by a pressure-induced change in hydrogen bonding. The stretching and bending vibrations of the water molecule are relatively unaffected by compression to 20 GPa, thus demonstrating that the structural cavities in which water molecules reside are relatively rigid. Significant changes in the amplitude of the O-H stretches of the hydroxyl and water units are observed at this pressure as well; nevertheless, our results demonstrate that the dominant structural units in lawsonite persist metastably at 300 K with only modest structural modifications well beyond the known stability field of this phase. Received: 10 July 1998 / Revised, accepted: 23 October 1998     

Groundwater contamination with arsenic and other trace elements in an area of the pampa,province of Córdoba,Argentina

A geochemical study of groundwater of the pampa in the province of Córdoba, Argentina, was performed; the area covered approximately 10,000 km².Physical-chemical parameters, dissolved solids, and seven trace elements were determined in 60 selected water samples. Systematic and accurate measurements of arsenic, flourine, and vanadium were performed for the first time. Three trace element contaminants not reported earlier were found: an important one, selenium, and two others of less known effects, uranium and molybdenum.Eighty-four percent of the water analyzed showed arsenic contents over 0.05 mg/L, maximum contaminant level established by the U.S. Environmental Protection Agency (1982). The frequency distribution of trace elements was analyzed, and its fit to the lognormal distribution was proved by means of the Pearson and Kolmogorov-Smirnov test; the geographic distribution of the seven trace elements was mapped and its correlation with the anion-cation composition of the water was studied.The maximum arsenic, fluorine, vanadium, and uranium contents were found in the western part of the area under study, in waters containing dominant alkali metals in the cation composition. Maximum selenium and antimony contents were found in the eastern part of the area, while molybdenum distribution does not show any relationship with the other two groups. In addition, the geographic distribution of the trace elements seems to be related to the subsurface structure, which has been inferred using interactive digital analysis of Landsat imagery. The movements of the subsoil have disturbed surface and subsurface drainage influencing the water salinity and trace element contents.In order to investigate the origin of the contamination, 54 loess samples were collected in wells at depths ranging from the surface down to the water table. This loess, which has a high proportion of volcanic components, mainly rhyolitic glass, exhibits a chemical composition corresponding to that of a dacite.The loess and the volcanic glass show anomalous contents of all contaminant trace elements, mainly arsenic and selenium. For this reason loess is considered the most important contamination source in the groundwater under study.