流体包裹体方法在油气源追踪对比中的应用——以四川盆地碳酸盐岩大型气田为例

本文运用流体包裹体方法，基于薄片观察和岩矿学研究，探讨了四川盆地碳酸盐岩大型气田的气源。首先对包裹体的生源属性、多期捕获和后生变化进行了精细的鉴别分析。在此基础上，通过成岩自生矿物微量元素、包裹体相组成、均一温度、初熔温度等参数鉴别多期演化的油气充注。通过烃类包裹体化学成分初步鉴别出煤成气和油型气。根据烃类包裹体的相组成鉴别有机质可能来源于腐泥型源岩还是腐殖型源岩。最后根据同期包裹体生物标志物确定某一期次的油气所对应的烃源层。结果表明研究成果符合地质实际，为传统的油气源追踪对比研究提供了一个重要有效的辅助方法。     

Hydrochemical and isotopic characteristics of groundwater in the Souss Upstream Basin, southwestern Morocco

Heterogeneous shallow Plio-Quaternary formations of the Souss Plain represent the most important aquifer in southern High Atlas Mountains in Morocco. The present work was conducted in the Souss Upstream Basin to identify the chemical characteristics and the origin of groundwater in an aquifer under semi-arid climate. Isotopic and hydrochemical compositions combined with geological and hydrogeological data were used for this purpose. The total dissolved solids vary from 239 to 997 mg l⁻¹, and the following groundwater types are recognized: Ca²⁺–Mg²⁺–HCO₃⁻, Ca²⁺–Mg²⁺–SO₄²⁻ and Ca²⁺–Mg²⁺–Cl⁻. The groundwater is saturated and slightly supersaturated with respect to carbonate minerals and undersaturated with respect to evaporite minerals, which means that the groundwater composition is largely controlled by the dissolution of carbonate rocks known in the basin. The isotopic contents of groundwaters ranged from −8‰ to −5.2‰ for δ¹⁸O, from −52‰ to −34‰ for δD, and from 0 to 5.5 TU for tritium. The hydrogen (δD) and oxygen (δ¹⁸O) isotope signatures reveal a significant infiltration before evaporation takes place, indicating a major recharge directly from fractures in the crystalline and limestone formations of Atlas Mountains (above 800 m a.s.l.) and infiltration of surface water in the alluvial cones at the border of the Atlas basins. The very low tritium values suggest that the groundwater recharge follows a long flow path and a mixing between old and modern water is shown. However, a slight evaporation effect is noted in the southern part of the basin close to the Anti-Atlas Mountains.     

Porewater pressure increases in soil and rock from underground chemical and nuclear explosions

A review and analysis of chemical and nuclear explosive-induced porewater pressure increases and induced rise in groundwater table elevations (groundwater mounding) is presented. Our analysis indicates that residual pore pressure increases and groundwater mounding can be induced by underground chemical and nuclear explosions to scaled distances of 879 m/(kt)^1/3. This relationship is linear over seven orders of magnitude of explosive energy ranging from a 0.01 kg chemical explosion to a 100 kt nuclear explosion and is valid for a wide variety of saturated geological profiles. Underground chemical explosions, and probably underground nuclear explosions have the potential to induce liquefaction of water-saturated soils to scaled distances of about 260 m/(kt)^1/3.     

滇西南澜沧群多硅白云母的多型和化学成分特征及其意义

从理论、实验及实际观察的结果都表明，随着压力的增加白云母中绿鳞石的含量显著地增加，可以认为在多期变质作用过程中，尤其是在变质压力不同的多期变质作用下，形成的多硅白云母，其化学成分就会打上不同的烙印。７７个多硅白云母化学成分的统计结果表明，澜沧群低级变质岩中的多硅白云母有两种成因。在Ｎａ－Ｍｇ相关图上，反映了高压和中压变质特征，高压变质的多硅白云母约占７０％。这与用多硅白云母ｂ０值鉴别的高压和中压变质是相吻合的。多硅白云母的多型为３Ｔ和２Ｍ１型，以２Ｍ１型为主     

黑龙江省东部跃进山群中绿片岩的地球化学特征及地质意义

跃进山群出露位于佳木斯地块和那丹哈达地体之间，是完达山造山带的组成部分。它由大陆斜坡相沉积物、大洋中脊型玄武岩和洋岛型玄武岩组成，其中有镁铁－超镁铁质岩块体。它不是一个地层单位，而是与活动大陆边缘板块俯冲作用有关的蛇绿混杂岩     

Qualitätsanforderungen an Oberflächengewässer: Zielvorgaben,Qualitätsziele und chemische Gewässergüteklassifizierung

Quality Requirements for Fresh Waters: Water Quality Targets, Water Quality Objectives, and Chemical Water Quality Classification In the Federal Republic of Germany, water quality requirements for the protection of inland surface waters against hazardous substances are formulated on the basis of a quality targets derivation concept developed jointly by the Federal Government and the Federal States. The quality requirements were termed “water quality targets” in order to make it clear that the values derived are orientational values rather than legally binding limit values. The international comparison of quality requirements for surface waters shows that, on the whole, the national quality targets ensure a high level of protection. According to present scientific knowledge, impairments of uses, such as supply of drinking water, or risks to aquatic communities need not to be expected if the quality targets are complied with. A comparison of water quality data with the water quality targets makes it possible, on the one hand, to identify those substances whose inputs must be further reduced; on the other hand, it also shows that, for a number of substances, there is no need at present for concern over their adversely water quality. A further differentiation of the aquatic hazard potential of pollutants allows a water quality classification system to be developed on the basis of the quality targets derivation concept. The basic elements of this water quality classification system are presented, and its application is explained by way of examples.     

榴辉岩的化学分类

以山东荣成地区的榴辉岩为例,把榴辉岩分为镁一榴辉岩、铁一榴辉岩和钙一榴辉岩三类。三类榴辉岩的岩石化学,主要造岩矿物成分都有明显差别,石榴石分别是镁铝榴石、铁铝榴石和钙铝榴石。绿辉石的硬玉分子也有不同。三类榴辉岩的化学成分限制是Mg-榴辉岩MgO>10%,石榴石以镁铝榴分子占优势,Fe-榴辉岩的MgO<10,石榴石以铁铝榴石分子占优势。Ca-榴辉岩CaO>19%,石榴石以钙铝榴石分子优势。     

西太平洋暖池热盐结构盐度场变异的主模态

基于1950~2011年间的月平均温、盐度资料,以28℃等温线作为西太平洋暖池的定义标准,并取ΔT=-0.4℃,分别计算了暖池区(20°N~15°S,120°E~140°W)各格点混合层、障碍层和深层的平均盐度,构成了暖池热盐结构的盐度场.据此,运用EOF分解法分析了暖池热盐结构盐度距平场主要模态的变化特征及其与ENSO间的关系,并探讨了主要模态的年际变异机理.结果表明,暖池热盐结构盐度场第一模态揭示了盐度场变异的关键区位于暖池中部;该模态具有2~4a的年际变化和准10a的年代际变化,并在1977年前后经历了一次气候跃变(此外,深层盐度场第一模态还在1999年前后发生了一次气候跃变),且在跃变前后与不同类型的ENSO事件有较密切的联系.暖池中部混合层和障碍层盐度的变化比较一致,即在跃变前盐度为偏高期,而在跃变后则变为偏低期.暖池中部深层盐度在1977年以前和1999年之后皆处于偏高期,而在1978~1999年间则处于偏低期.而且,从混合层至深层,盐度的变化幅度逐渐变小.进一步分析表明,暖池中部混合层和障碍层盐度的年际变化主要是由纬向风、南赤道流(SEC)和降水共同引起的,即当东风增强(减弱)时,强(弱)SEC将携带更多(少)的高盐水进入混合层或潜沉至障碍层,同时局地降水的减少(增多),也使得混合层和障碍层的盐度增加(减少);深层盐度的年际变化主要是由SEC和赤道潜流(EUC)导致的,即当SEC增强(减弱)时,将有更多(少)的高盐水进入暖池,而当EUC增强(减弱)时则有更多(少)的低盐水流出暖池,从而使得暖池的深层盐度升高(降低).     

Whole-rock chemistry of the Gameleira I uranium deposit,Lagoa Real,Brazil

The Lagoa Real uranium (U) province, referred to as Lagoa Real, is located in the state of Bahia, north-eastern Brazil. Lagoa Real has ∼112,000 metric tonnes and average grade of 2700 ppm of U₃O₈, being one of the largest U deposits in the world and the largest in Brazil. Despite its economic and strategic importance, there are gaps in the geological knowledge of the Lagoa Real U deposits. One of them is the lack of extensive whole-rock chemical data sets. Here, we present whole-rock chemical analyses for major and trace elements, including the rare-earth elements (REE), from barren country rocks to uraniferous ore shoot, systematically sampled from an exploratory drill hole. The chemical data indicate that albitite rocks, with and without uraniferous mineralisation, cannot result from sodic syenitic magmatism, as proposed by recent studies. Petrographical and geochemical evidence supports the previously suggested concept that the Lagoa Real albitite rocks resulted from sodic metasomatism of the granitic country rock, known as the São Timóteo granite. Their ore-mineral assemblages and geochemical characteristics are similar to albitite-hosted U deposits worldwide.     

Formation and stability of mixed Mg/Ca/phytate species in synthetic seawater media: Consequences on ligand speciation

The results of a potentiometric investigation (by ISE-H⁺, glass electrode) on the speciation of phytate ion (Phy¹²⁻) in an ionic medium simulating the major components (Na⁺, K⁺, Ca²⁺, Mg²⁺, Cl⁻ and SO₄²⁻) of natural seawater, at different salinities and t = 25 °C, are reported. The work was particularly aimed at determining the possible formation of mixed Ca²⁺–Mg²⁺–phytate ion pairs, and to establish how including the formation of these mixed species would affect the speciation modeling in seawater media. After testing various speciation models, that considering the formation of the MgCaH₃Phy⁵⁻, MgCaH₄Phy⁴⁻, Mg₂CaH₃Phy³⁻ and Mg₂CaH₄Phy²⁻ species was accepted, and corresponding stability constants were determined at two salinities (S = 5, 10). A discussion is reported both on the choice of the experimental conditions and on the possibility to extend these results to those typical of real seawater. A detailed procedure is also described to demonstrate that the stability of these species is higher than that statistically predicted. As reported in literature, a parameter, namely log X, has been determined in order to quantify this extra stability for the formation of each mixed species at various salinities. For example, at S = 10, log X₁₁₃ = 2.67 and log X₁₁₄ = 1.37 for MgCaH₃Phy⁵⁻ and MgCaH₄Phy⁴⁻ (statistical value is log X_stat = 0.60), and log X₂₁₃ = 6.11 and log X₂₁₄ = 2.15 for Mg₂CaH₃Phy³⁻ and Mg₂CaH₄Phy²⁻ (log X_stat = 1.43), respectively. Results obtained also showed that the formation of these species may occur even in conditions of low salinity (i.e. low concentration of alkaline earth cations) and low pH (i.e., more protonated ligand).