Hydrogen Isotope Study of Fluid Inclusions in Vein Quartz of the Hishikari Gold Deposits, Japan

Abstract: The origin of mineralizing fluids responsible for the Hishikari vein-type epithermal Au deposits was studied on the basis of the hydrogen isotopic ratio (δD) of the inclusion fluid from vein quartz and adularia. The origin of hydrothermal fluids was estimated by combination of the present δ values and the oxygen isotopic ratios (δ¹⁸O) previously reported by Shikazono and Nagayama (1993). The water in the fluid inclusions was extracted by means of decrepitation of quartz at 500°C. Hydrogen was obtained by reduction of the collected water with Zn shot at 450°C. The δD values were determined by mass spectrometer. The δD values of inclusion fluid obtained from quartz range from –61 to –114%. These are significantly lower than the δD value of the thermal water presently venting from the Hishikari deposits and that of local meteoric water. Hydrogen isotopic fractionation between water and amorphous silica, which might have initially precipitated from the hydrothermal fluids at least partly, is not a probable cause of this isotopic depletion, while some water might have been released from the initial hydrous amorphous silica during recrystallization to quartz observed presently. Thus, a part of ore fluids for the Hishikari deposits is supposed to have been originated from the water having anomalous δD values of lower than –100%. Such D depletion cannot be caused by simple oxygen-shift of meteoric water or by contribution of magmatic volatiles. The δD values of water released from the shale samples of the Shimanto–Supergroup, a major host to the Hishikari veins range from –132 to –148%. Therefore, the anomalous δD values of inclusion fluids from some vein quartz and adularia suggest that the water released from hydrous minerals of the sedimentary basement rocks by dehydration or the groundwater isotopically exchanged with sedimentary rocks at elevated temperatures during circulation, partly contributed to the hydrothermal fluids responsible for the Hishikari deposits.     

橄榄石热解氢释放过程的分析

采用分步法热法分析了不同粒度的橄榄石的Ｈ２的质量体系,实验表明,不同粒度的橄榄石释放出的Ｈ２的质量体积不同,随着温度或粒度的变化,Ｈ２的质量体积呈现出规律性的变化,进一步探讨了氢在橄榄石中的赋存状态。     

轻烃及硫化物气体测量找寻多金属隐伏矿方法试验

挥发性有机化合物及硫化物气体作指标勘查金属矿床的工作国内外均处于初试阶段。近几年我们用硫化氢、二氧化硫及轻烃气体(C₁—C₄烷烃和烯烃)作指标对十个不同景观条件不同地区的铅锌矿、铜钼矿、金矿、铜镍等多金属矿床进行了土壤及地表岩石测量勘查隐伏矿的方法试验,取得很好的结果。表明该方法是寻找多金属隐伏矿的一种有效的气体测量方法,它可用于寻找覆盖厚度几米到400多米运积物覆盖区隐伏矿及基岩面下埋藏400多米盲矿的地表土壤和岩石测量以及岩体评价找矿工作。试验结果还表明该方法用于岩石测量的效果优于土壤测量。     

The annual cycle of peroxides and ozone in marine air at Cape Grim, Tasmania

The concentration of gas-phase peroxides has been measured almost continuously at the Cape Grim baseline station (41° S) over a period of 393 days (7702 h of on-line measurements) between February 1991 and March 1992. In unpolluted marine air a distinct seasonal cycle in concentration was evident, from a monthly mean value of>1.4 ppbv in summer (December) to <0.2 ppbv in winter (July). In the summer months a distinct diurnal cycle in peroxides was also observed in clean marine air, with a daytime build-up in concentration and decay overnight. Both the seasonal and diurnal cycles of peroxides concentration were anticorrelated with ozone concentration, and were largely explicable using a simple photochemical box model of the marine boundary layer in which the central processes were daytime photolytic destruction of ozone, transfer of reactive oxygen into the peroxides under the low-NO_x ambient conditions that favour self-reaction between peroxy radicals, and continuous heterogeneous removal of peroxides at the ocean surface. Additional factors affecting peroxides concentrations at intermediate timescales (days to a week) were a dependence on air mass origin, with air masses arriving at Cape Grim from higher latitudes having lower peroxides concentrations, a dependence on local wind speed, with higher peroxides concentrations at lower wind speeds, and a systematic decrease in peroxides concentration during periods of rainfall. Possible physical mechanisms for these synoptic scale dependencies are discussed.     

Laboratory studies of some environmental variables controlling sulfur emissions from plants

Several trace sulfur gases that can have a significant influence on atmospheric chemistry are emitted from biological systems. In order to begin to address biological questions on the mechnisms of production of such gases, laboratory-scale experiments have been developed that reproduce such emissions under controlled conditions. Using a flux chamber technique, flats containing soil, or soil plus plants were sampled for the net fluxes of sulfur gases. The major sulfur gas emitted from all the plants tested (corn, alfalfa, and wheat) was dimethyl sulfide (DMS). Alfalfa and wheat also emitted lesser amounts of methanethiol, variable amounls of hydrogen sulfide, and in some experiments wheat emitted carbon disulfide. The use of a plant incubator allowed a systematic study of the effects of variables such as temperature, photon flux, and carbon dioxide levels, on these emissions. Fluxes of all the emitted sulfur gases increased exponentially with increasing air temperature, and increased with increasing photon flux up to a saturation level of \~300 E/m^–2 sec^-1. Three to four-fold changes in DMS flux were observed during light to dark or dark to light transitions. By varying the CO₂ content of the chamber flush gas, it was shown that the observed sulfur fluxes from corn and alfalfa were not related to the CO₂ concentration. Growing these crop plants through holes in a Teflon soil-covering film allowed a separate determination of soil and foliage emissions and substantiation of the light dependent uptake of COS by growing vegetation observed in previous field studies.     

Study of metal aerosol systems as a sink for atmospheric SO2

The chemical removal of SO₂ in the presence of different aerosol systems has been investigated in laboratory experiments using a dynamic flow reactor. The aerosols consisted of wetted particles containing one of the following substances: MnCl₂, Mn(NO₃)₂, MnSO₄, CuCl₂, Cu(NO₃)₂, CuSO₄, FeCl₃, NaCl. The SO₂ removal rate R was measured as a function of the SO₂ gas phase concentration (SO₂)_g, the spatial metal concentration C_Me, and the relative humidity rH in the reactor. A first-order dependence with regard to (SO₂)_g was observed for each type of aerosol. For the Mn(II) and Cu(II) aerosols R was found to be a non-linear function of C_Me except for MnSO₄ and Cu(NO₃)₂ particles. The removal rate showed a significant increase with the relative humidity particularly when rH was close to the deliquescence point of the wetted particles. Among the Mn(II) and Cu(II) aerosols investigated Mn(NO₃)₂ was found to be most efficient for the chemical removal of SO₂ at atmospheric background conditions, especially in haze and fog droplets. The results further indicate that the catalytic oxidation of S(IV) in such aerosol systems may be as efficient as its oxidation by H₂O₂ in cloud water.     

SOHM-4型氢原子钟的设计改进与初步性能

氢原子钟是一种最稳定的 (除极短测量时间间隔之外 )频率标准 ,但是环境温度变化及微波谐振腔老化会引起原子钟输出频率的变化 ,从而导致氢原子钟长期性能变差。为了减小这些影响 ,可借助一种自动调谐器来确保谐振腔的频率始终工作在所需的频率上 ,并采用新的温度控制系统来改善氢原子钟的长期性能。针对这些年来许多氢钟出现的有关问题 ,上海天文台在借鉴国外氢钟实验室经验的基础之上 ,对原有氢钟进行了技术改造 ,并为国家授时中心研制了SOHM - 4型氢原子钟。对该型氢原子钟技术改造特点作了介绍 ,并给出了期望的性能指标及初步的测试结果     

Water organisation at the solid–aqueous solution interfaceOrganisation de l'eau à l'interface solide–solution aqueuse

The aim of this review is to examine the present knowledge about water structure close to an interface or confined in porous spaces. First, the structure of liquid water is briefly described. Though its understanding remains incomplete, it appears that it is largely dominated by the hydrogen bond network and its dynamical evolution. The presence of any ‘foreign’ substance in water perturbs such a structure by changing at least locally the hydrogen bond network. For this reason, the presence of a solid interface significantly modifies the structure of the first adsorbed layers. Whatever the support, it is now clearly evidenced that structural perturbations are limited to distances lower than 10–15 Å from the interface. The nature, energetic heterogeneity and hydrophilicility/hydrophobicity of the solid surface influence the arrangement of water molecules. This surface organisation must definitely be considered when studying adsorption phenomena at the solid–aqueous solution interface. The relevance of such problems to geosciences is illustrated by a few situations in which water structure plays a prominent role. To cite this article: L.J. Michot et al., C. R. Geoscience 334 (2002) 611–631.     

热解色谱分析技术在伊犁盆地 铀矿床干酪根地球化学研究中的应用

利用伊利盆地砂岩型铀矿床干酪根热解色谱数据,计算获得氢指数、氧指数等重要指标,在此基础上,应用氢指数、氧指数划分了伊犁盆地铀矿床干酪根类型,再依据烃指数和产率指数对伊犁盆地铀矿床干酪根的成熟度进行了初步评价。     

Using stable isotopes to quantify water sources for trees and shrubs in a riparian cottonwood ecosystem in flood and drought years

Riparian cottonwood forests in dry regions of western North America do not typically receive sufficient growing season precipitation to completely support their relatively high transpiration requirements. Water used in transpiration by riparian ecosystems must include alluvial groundwater or water stored in the potentially large reservoir of the unsaturated soil zone. We used the stable oxygen and hydrogen isotope composition of stem xylem water to evaluate water sources used by the dominant riparian cottonwood (Populus spp.) trees and shrubs (Shepherdia argentea and Symphoricarpos occidentalis) in Lethbridge, Alberta, during 3 years of contrasting environmental conditions. Cottonwoods did not exclusively take up alluvial groundwater but made extensive use of water sourced from the unsaturated soil zone. The oxygen and hydrogen isotope compositions of cottonwood stem water did not strongly overlap with those of alluvial groundwater, which were closely associated with the local meteoric water line. Instead, cottonwood stem water δ¹⁸O and δ²H values were located below the local meteoric water line, forming a line with a low slope that was indicative of water exposed to evaporative enrichment of heavy isotopes. In addition, cottonwood xylem water isotope compositions had negative values of deuterium excess (d‐excess) and line‐conditioned (deuterium) excess (lc‐excess), both of which provided evidence that water taken up by the cottonwoods had been exposed to fractionation during evaporation. The shrub species had lower values of d‐excess and lc‐excess than had the cottonwood trees due to shallower rooting depths, and the d‐excess values declined during the growing season, as shallow soil water that was taken up by the plants was exposed to increasing, cumulative evaporative enrichment. The apparent differences in functional rooting pattern between cottonwoods and the shrub species, strongly influenced the ratio of net photosynthesis to stomatal conductance (intrinsic water‐use efficiency), as shown by variation among species in the δ¹³C values of leaf tissue.