呼伦湖流域氢氧稳定同位素特征及其对水体蒸发的指示作用

以呼伦湖流域为例研究该区域氢氧稳定同位素在不同水体中的分布特征,并探讨氢氧稳定同位素对在该区域水文过程的指示作用.流域湖水、入湖河水、周边地下水水样的氢氧稳定同位素分析结果表明,夏季8月份湖水中的重氢氧稳定同位素比7月份的更加富集.而河水中氢氧稳定同位素在同一时间内的河流沿程上存在明显的差异,下游水体中的氢氧稳定同位素要比上游更加富集.研究区的河水和湖水的δ~(18)O-δD关系特征显示,河水和湖水的δ~(18)O-δD的关系点全部位于当地降水线的右下方,说明流域河水和湖水水体受到明显的蒸发作用.而井水的δ~(18)O-δD的关系点大都靠近当地大气降水线,说明这一区域的地下水主要是大气降水渗入地下形成.利用氢氧稳定同位素分馏过程中的氢氧稳定同位素的比率与剩余水体的关系,并在考虑湿度因子的动力分馏模拟下,计算出河水的剩余水体比例在0.85~0.96之间,而湖水的剩余水体比例在0.71~0.77之间.最后,利用氢氧稳定同位素质量平衡法对呼伦湖多年平均蒸发量进行了估算,估算的湖泊蒸发量结果与实测值相近,相对误差为5.4%,说明方法可靠.氢氧稳定同位素对于研究区域水文过程有着重要的作用,在今后呼伦湖流域水文研究中有着更加广泛的应用空间.     

Subterranean microorganisms and radioactive waste disposal in Sweden

In 1987, microbiology became a part of the Swedish scientific program for the safe disposal of high level nuclear waste (HLW). The goal of the microbiology program is to understand how subterranean microorganisms will interact with the performance of a future HLW repository. The Swedish research program on subterranean microbiology has mainly been performed at two sites in granitic rock aquifers at depths ranging from 70 m down to 1240 m, the Stripa research mine in the middle of Sweden and the Äspö Hard Rock Laboratory (HRL) situated on the south eastern coast of Sweden. Some work has also been performed in cooperation with other national or international research groups in Sweden, Canada and at the natural analogue sites Oklo in Gabon and Maqarin in Jordan. The following conclusions are drawn. There is a very high probability of the existence of a deep subterranean biosphere in granitic rock. The documented presence of a deep biosphere implies that relevant microbial reactions should be included in the performance assessment for a HLW repository. A HLW repository will be situated in a subterranean biosphere that is independent of solar energy and photosynthetically produced organic carbon. The ultimate limitation for an active microbial life will be the availability of hydrogen as energy source over time, and hydrogen has indeed been found in most deep groundwaters. Sulphide producing microorganisms are active in environments typical for a Swedish HLW repository, and the potential for microbial corrosion of the copper canisters must be considered. The bentonite buffer around the copper canisters will be a hostile environment for most microbes due to the combination of radiation, heat and low water availability. Discrete microbial species can cope with each of these constraints, and it is theoretically possible that sulphide producing microbes may be active inside a buffer, although the experiments conducted thus far have shown the opposite. Microorganisms have the capability to enzymatically recombine radiolysis oxidants formed by radiation of water. It has earlier been concluded that the migration of radionuclides due to sorption on microorganisms can be neglected. The influence of microbially produced complexing agents remains to be studied at realistic conditions in deep groundwater. Microorganisms have been found in natural alkaline groundwaters, but it could not be conclusively demonstrated that they were in situ viable and growing, rather than just transported there from neutral groundwater. A possible hypothesis based on the obtained results from investigations of natural alkaline groundwaters is that fresh concrete may be a bit too extreme for active life even for the most adaptable microbe – but this remains to be demonstrated.     

生物制氢:Ⅰ.理论研究进展

对生物制氢的理论研究进行了评论性的回顾。讨论了光合成生物制氢系统、光分解生物制氢系统、水气交换反应生物制氢系统、光合—发酵杂交生物制氢系统和厌氧发酵生物制氢系统、离体氢酶生物制氢系统等6个生物制氢系统。乙醇型发酵生物制氢理论(双碳发酵产氢学说或理论)是生物制氢理论的新发展。     

河北平原地下水氘过量参数特征

氘过量参数是由Dansg aar d提出的一个新概念,它被定义为:d= δD-8δ18O。河北平原地下水氘过量参数有三个特征: ( 1)地下热水的氢和氧同位素组成显示出热交换的态势,d 值随地下水年龄增大而减少。( 2)在同一地区,d 值随着地下水埋深加大而增大。( 3)在同一含水层内,沿着地下水的路径,从补给区到承压区, d 值随着地下水年龄增大而增大。我们认为, d 值虽然是地下水年龄的函数,但最好和3 H、3H- 3He、14 C、36 Cl和4 He测年结果结合使用。      

Mercury in the Tinto-Odiel Estuarine System (Gulf of Cádiz, Spain): Sources and Dispersion

The Tinto and Odiel are small rivers draining one of the largest sulphide deposits in the world. As a result of these deposits and a large industrial complex, the adjacent marine area receives a high amount of metal input. Mercury distribution in the Tinto-Odiel estuary, the Huelva Ría and the Gulf of Cádiz was assessed in water and suspended particulatematter (SPM) and sediments. In the rivers and estuaries, dissolved (HgD)and particulate (HgP) mercury showed wide variations (13 to 200 pM and0.3 to 330 nmol g^-1 respectively) depending on the presence or notof sulphidic waters, phosphogypsum deposits, detrital pyrite and oxyhydroxides.In the Ría, concentrations were lower than 10 pM and 4.5 nmol g^-1 for HgD and HgP respectively. In surface waters of the Gulf of Cádiz, the average HgD concentration (pm standard deviation) was 2.9 pm 0.9 pM, which is similar to that of North Atlantic Central Waters. The surface sediments collected in the rivers, the Ría and the Gulf showed systematically enriched mercury compared to pre-industrial levels. Vertical mercury profiles in dated sediment cores were typical of anthropogenically influenced environments starting in the early Roman age. These distribution features suggest that most of the Hg discharged by the Huelva Ría is trapped in the sediments of the Gulf of Cádiz.     

An infrared and <Superscript>1</Superscript>H MAS NMR investigation of strong hydrogen bonding in ussingite,Na<Subscript>2</Subscript>AlSi<Subscript>3</Subscript>O<Subscript>8</Subscript>(OH)

The mineral ussingite, Na₂AlSi₃O₈(OH), an interrupted tectosilicate, has strong hydrogen bonding between OH and the other nonbridging oxygen atom in the structure. Infrared spectra contain a strongly polarized, very broad OH-stretching band with an ill-defined maximum between 1500 and 1800 cm^–1, and a possible OH librational bending mode at 1295 cm^–1. The IR spectra confirm the orientation of the OH vector within the triclinic unit cell as determined from X-ray refinement (Rossi et al. 1974). There are three distinct bands in the ¹H NMR spectrum of ussingite: a predominant band at 13.5 ppm (TMS) representing 90% of the structural hydrogen, a second band at 15.9 ppm corresponding to 8% of the protons, and a third band at 11.0 ppm accounting for the remaining 2% of structural hydrogen. From the correlation between hydrogen bond length and ¹H NMR chemical shift (Sternberg and Brunner 1994), the predominant hydrogen bond length (H...O) was calculated to be 1.49 Å, in comparison to the hydrogen bond length determined from X-ray refinement (1.54 Å). The population of protons at 15.9 ppm is consistent with 5–8% Al–Si disorder. Although the ussingite crystal structure and composition are similar to those of low albite, the bonding environment of OH in low albite and other feldspars, as characterized through IR and ¹H NMR, is fundamentally different from the strong hydrogen bonding found in ussingite.     

块状硫化物矿石中硫化物的压溶和增生及成矿意义——以加拿大西部矿床为例

加拿大西部块状硫化物矿石普遍地发生过硫化物的压溶和增生。增生作用根据增生体的成分可以分为同质增生和异质增生，根据动力环境可以分为静态增生和动态增生。三晶嵌接结构可以是静态增生的产物。压溶和增生是块状硫化物矿床成岩和变质过程中的重要作用。脉石矿物的压溶可使原生矿石就地加富，硫化物的压溶可使成矿物质发生再活化。增生可促进矿质沉淀。富含硫化物的地层之所以能成为地球化学障而有利于后期热液叠加和层控矿床的形成，硫化物晶芽的增生是一种重要机制。     

滇东南安那金矿床成矿流体地球化学研究

云南安那金矿床位于右江盆地南缘,产于二叠纪辉绿岩侵入体之中,广泛发育乳白色石英网脉,蚀变辉绿岩体即为金矿体。与右江盆地以沉积岩为容矿岩石的卡林型金矿床类似,具有硅化、粘土化、碳酸盐化和硫化物化等热液蚀变特征。本文对安那金矿床石英中的流体包裹体岩相学、显微测温学、激光拉曼光谱以及氢氧同位素组成进行了分析,发现成矿期石英中的流体包裹体主要为富含CO_2气-液两相或三相流体包裹体,其均一温度范围为208~312℃(平均254℃),盐度很低,变化范围为0~2%Na Cleqv,成矿溶液的密度为0.88~0.98g/cm~3,表明形成安那金矿床的成矿流体属于中温、低盐度、中-低密度的流体。激光拉曼光谱分析显示,石英中包裹体的气相成分富含CO_2、N_2以及微量CH_4等挥发分。成矿流体的氢氧同位素组成显示变质流体成因,结合矿石显微岩相学结构,认为流体溶蚀交代辉绿岩中的含Ti-Fe辉石或者钛铁矿,溶解Fe的硫化作用过程是含Au黄铁矿和毒砂沉淀富集的重要机制。成矿作用可能与右江盆地南缘印支期造山事件有关。     

EPR investigation of the methyl radical,the hydrogen atom and carbon oxide radicals in Maxixe-type beryl

The EPR spectra of Maxixe-type beryl contain a large number of overlapping signals. The angular dependence of the 1:3:3:1 signal typical for the CH₃ radical shows that this radical is located at the center of the channel cavity with its symmetry axis parallel to the crystal c-axis and is rotating around this axis. Its EPR spectrum is axially symmetric with g _// = 2.00263, g _⊥ = 2.00249 and A_// = 2.288 mT, A_⊥ = 2.256 mT. These anisotropies have the opposite signs of those found for surface-adsorbed methyl radicals. Hydrogen atoms are located at position 2a at the center of the beryl cavity and the EPR parameters of the narrow doublet signal are A ₀ = 1,407 MHz and g = 2.00230. Another doublet signal, which is broader and has axial symmetry with g _// = 2.00265, g _⊥ = 2.00625 and A_// = 0.895 mT, A_⊥ = 0.885 mT, could come from a HCO₃ radical. One narrow and easily saturated signal with g _// = 2.00227 and g _⊥ = 2.00386 is interpreted to arise from a carbon monoxide radical in the beryl channel, oriented with its axis parallel to the crystal c-axis. Additional weak doublet lines, which have similar g values as the carbon monoxide radical, are created by nearby hydrogens. A powder spectrum with g _// = 2.0017 and g _⊥ = 2.0004 appears upon UV irradiation of the single crystal and is easily saturated. This spectrum is interpreted to arise from a carbon dioxide radical, which rotates around its symmetry axis.