澜沧江云南德钦古水一带第四纪堰塞湖的沉积特征及其环境意义

在云南省西北部德钦县古水一带深切的澜沧江河谷中,发现了一套第四纪湖相沉积物,以纹层状粘土、粉砂质粘土和粉砂的互层组合为特征,构成了第三和第四级阶地的基座.笔者对该湖相剖面进行了U系、孢粉和若干地球化学指标的分析测试,并以这些结果讨论了古湖的形成时代和成因,以及古湖堆积时期的古植被和古气候.剖面顶部、中部和中下部粘土的U系法年龄测定结果分别为52.3±3.4 ka、64.2±5.6 ka和81.9±6.5 ka,说明古水古湖形成于晚更新世早中期的末次间冰期晚期和末次冰期的早冰阶与间冰阶早期,很可能是大型冰川(如下游的明永冰川等)或巨量的冰水沉积物堰塞了澜沧江河谷而造成的结果.     

柴达木盆地北缘侏罗系不同沉积环境烃源岩生物标志物特征及其应用

柴达木盆地北缘地区侏罗系(中下侏罗统)的优质烃源岩主要发育于湖相与三角洲相环境。研究了不同时代、不同沉积环境中烃源岩的生物标志物组成特征,结果发现,有3类化合物的分布与组成差异显著,包括三环萜烷(C19、C20、C21)的分布型式、重排藿烷的丰度以及规则甾烷的相对组成。其中,不同时代的差异主要体现在规则甾烷组成上;而不同沉积环境的差异主要体现为三环萜烷(C19、C20、C21)的分布型式及重排藿烷的丰度。分析认为,这些差异与烃源岩的沉积环境及其生源组成有密切关系。据此,初步将这些参数应用于两方面研究,一是为划分地层沉积环境提供“生物标志物相标志”,二是研究油源对比,取得良好效果。因此,本文研究结果具有重要实用价值与参考意义。     

An experimental study of the grain-scale processes of peridotite melting: implications for major and trace element distribution during equilibrium and disequilibrium melting

The grain-scale processes of peridotite melting were examined at 1,340°C and 1.5 GPa using reaction couples formed by juxtaposing pre-synthesized clinopyroxenite against pre-synthesized orthopyroxenite or harzburgite in graphite and platinum-lined molybdenum capsules. Reaction between the clinopyroxene and orthopyroxene-rich aggregates produces a melt-enriched, orthopyroxene-free, olivine + clinopyroxene reactive boundary layer. Major and trace element abundance in clinopyroxene vary systematically across the reactive boundary layer with compositional trends similar to the published clinopyroxene core-to-rim compositional variations in the bulk lherzolite partial melting studies conducted at similar P–T conditions. The growth of the reactive boundary layer takes place at the expense of the orthopyroxenite or harzburgite and is consistent with grain-scale processes that involve dissolution, precipitation, reprecipitation, and diffusive exchange between the interstitial melt and surrounding crystals. An important consequence of dissolution–reprecipitation during crystal-melt interaction is the dramatic decrease in diffusive reequilibration time between coexisting minerals and melt. This effect is especially important for high charged, slow diffusing cations during peridotite melting and melt-rock reaction. Apparent clinopyroxene-melt partition coefficients for REE, Sr, Y, Ti, and Zr, measured from reprecipitated clinopyroxene and coexisting melt in the reactive boundary layer, approach their equilibrium values reported in the literature. Disequilibrium melting models based on volume diffusion in solid limited mechanism are likely to significantly underestimate the rates at which major and trace elements in residual minerals reequilibrate with their surrounding melt. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Simple models for dynamic melting in an upwelling heterogeneous mantle column: Analytical solutions

Several lines of evidence suggest that the melt generation and segregation regions of the mantle are heterogeneous, consisting of chemically and lithologically distinct domains of variable size and dimension. Partial melting of such heterogeneous mantle source regions gives rise to a diverse range of basaltic magmas. In order to better assess the role of source heterogeneity during mantle melting, we have undertaken a theoretical study of trace element distribution and fractionation during concurrent melting and melt migration in an upwelling, chemically heterogeneous, two-porosity double lithology melting column. Analytical solutions for the abundance of a trace element in the matrix and channel were obtained under the assumptions that the porosity, melt and solid velocities, and solid-melt partition coefficients are constant and uniform. For simplicity, we neglected diffusion and dispersion in the melt. Chemical source heterogeneities of arbitrary size and shape were integrated into the simple melting models by allowing trace element abundance in the source region to vary as a function of time and space. Concurrent melting and melt migration in an upwelling heterogeneous mantle may be approximated as a quasi-steady state problem in which time-dependent concentration patterns produced by melting of heterogeneous source regions are superimposed on a reference steady-state concentration distribution established by melting of the ambient or background mantle. Chromatographic fractionation is especially important for the matrix melt and solid when chemical heterogeneities are involved during melting and melt migration in the mantle, giving rise to significant phase-shift between two incompatible trace elements in the matrix melt and scattered correlations among incompatible trace elements in residual peridotites. Mixing is the chief mass transfer process in the dunite channel where the chromatographic effect is negligible for most of the incompatible trace elements. The lack of chromatographic fractionation among incompatible trace elements and isotopic ratios in MORB suggests either most MORB are channel melts or mixing in magma conduit and chamber is very efficient such that the phase-shift is averaged out during magma transport and storage processes. Advection brings melt produced by smaller-degree of melting in the deeper part of the melting column to the overlying melting region, increasing the incompatible trace element abundance in the matrix and the channel. This advection-induced self-enrichment is especially important when heterogeneous sources are involved and may account for some of the enriched incompatible trace element patterns observed in residual peridotite that were previously interpreted to be a result of mantle metasomatism. Systematic studies of high-resolution spatially correlated mantle samples may help to constrain the melting history and the size and nature of chemical heterogeneities in the mantle.     

Considerations for conducting incubations to study the mechanisms of As release in reducing groundwater aquifers

Microbial Fe reduction is widely believed to be the primary mechanism of As release from aquifer sands in Bangladesh, but alternative explanations have been proposed. Long-term incubation studies using natural aquifer material are one way to address such divergent views. This study addresses two issues related to this approach: (1) the need for suitable abiotic controls and (2) the spatial variability of the composition of aquifer sands. Four sterilization techniques were examined using orange-colored Pleistocene sediment from Bangladesh and artificial groundwater over 8 months. Acetate (10 mM) was added to sacrificial vials before sterilization using either (1) 25 kGy of gamma irradiation, (2) three 1-h autoclave cycles, (3) a single addition of an antibiotic mixture at 1× or (4) 10× the typical dose, and (5) a 10 mM addition of azide. The effectiveness of sterilization was evaluated using two indicators of microbial Fe reduction, changes in diffuse spectral reflectance and leachable Fe(II)/Fe ratios, as well as changes in P-extractable As concentrations in the solid phase. A low dose of antibiotics was ineffective after 70 days, whereas autoclaving significantly altered groundwater composition. Gamma irradiation, a high dose of antibiotics, and azide were effective for the duration of the experiment.     

黔东震旦系—下寒武统黑色岩系稀土元素地球化学特征

：通过对黔东丹寨南皋剖面和三都渣拉沟剖面的稀土元素分析发现：两条剖面的梅树村期与筇竹寺期 分界处大量稀土元素明显富集,黑色页岩中存在明显的Ｃｅ负异常和Ｅｕ、Ｙ 正异常,表明为缺氧和热水沉积的产物。 这套黑色岩系总体沉积于缺氧和具热水注入的环境中,但发生缺氧和热水注入的时间和强度在不同地方会有不同 的表现。     

利用MC-ICPMS对水样中硼同位素比值的测定

采用Amberlite IRA-743硼特效树脂进行水溶液中硼的分离,对洗脱液温度、体积以及树脂动态交换容量等进行了实验.它的动态交换容量为4.2 mg/g,在室温条件下,用5 mL 2%HNO3可定量从树脂柱上洗脱被吸附的硼.采用Neptune型MC-ICPMS进行硼同位素组成的测定,1 μg/g浓度的硼标准溶液获得放大的信号强度约为0.7V,硼的化学分离过程有效避免了质量歧视效应.实验结果表明,MC-ICPMS对硼存在严重的记忆效应,通过采用5%HNO3-(1%HNO3 0.1%HF)-H2O-20%NH3H2O-H2O的交替清洗方法,可在约1 h内消除硼的记忆效应.在最佳仪器条件下,对含有250 ng硼的水样,可以快速测定硼的同位素组成,占δ11B测定的绝对偏差为0.4‰-0.5‰(SD).     

广州大气降水中δ^18O与气象要素及季风活动之间的关系

根据2004年5月至2005年6月广州日大气降水中δ18O资料和GNIP提供的广州、香港多年月平均降水中δ D、δ18O资料, 研究了天气尺度下广州大气降水中δ18O与降水量、水汽压、气温和露点温度等气象要素之间的关系, 并就季风活动对本地降水中δ18O的影响作了初步分析. 结果表明: 在天气尺度下, 广州大气降水中δ18O与降水量、水汽压、气温和露点温度均存在显著的负相关关系, 同温度露点差存在显著的正相关关系, 表明广州大气降水中δ18O变化具有显著的降水量效应和湿度效应. 夏季风期间季风活动对天气尺度下降水中δ18O的变化具有显著影响, 使得天气尺度下大气降水中δ18O变化有时并不遵循降水量效应. 从多年气候平均状况来看, 广州、香港降水中δ18O的季节变化同亚洲夏季风的爆发和推进演变过程较为相似, 在夏季风活跃的时期, 大气降水中δ18O值也较低, 反映了季风降水再循环活动对降水中稳定同位素含量具有显著影响.     

西宁地区大气中黑碳气溶胶浓度的观测研究

对2005年9月至2007年7月在西宁获得的黑碳气溶胶(BC)浓度观测资料及气象观测资料进行了分析. 结果表明, 受当地冬季取暖和冬季逆温出现频率高的影响, BC浓度的月际变化规律明显, 且变化幅度大, BC浓度高值出现在每年10月至次年1月;低值出现在5-8月;日平均浓度为4 240.1 ng·m-3, 其变化范围为957.5～11 045.5 ng·m-3. 受局地人为活动和大气垂直对流扩散等影响, BC浓度日变化表现出明显的双峰值特征, BC高浓度出现在7:00～12:00和18:00～24:00, 而低浓度一般出现在14:00～17:00和02:00～05:00时段. 与相距90 km的瓦里关全球本底站相比, 西宁BC日平均浓度偏高约13倍, 且月际变化差异大, 但与国内部分城市相比还是较低(除西藏拉萨外).     

中国-俄罗斯原油管道工程(漠河-大庆段)冻土工程地质考察与研究进展

在2005-2007年期间,先后3次对中国-俄罗斯原油管道漠河-大庆段沿线的冻土工程地质条件等进行科学考察,开展了冻土工程地质条件及其在气候变化和人类活动作用下的评价和预测研究.考察研究结果表明:管道沿线多年冻土在各类融区、季节冻土和水系等分隔作用下呈片状或岛状分布,沿线岛状、稀疏岛状及零星岛状占多年冻土区段的40%左右;管道沿线多年冻土随着气候的转暖和人类活动的影响不断退化.地形地貌单元、植被分布、地表水分条件的变化等局部因素对多年冻土的分布和地下冰的赋存产生重要的影响,管道沿线大约分布有50 km左右的沼泽湿地,其表层为腐殖质土及泥炭层,泥炭层下面分布着含土冰层或地下冰,是管道沿线最差的冻土工程地质地段;由于中俄原油管道沿线水系发育多,冻胀丘、冰椎和冰幔等不良冻土现象广泛分布.科学考察的成果为管道沿线冻土工程地质条件评价和预测、管道的稳定性影响分析以及后期的长期检测系统设置等研究奠定坚实的基础,进一步为即将开工的中俄原油管道漠河-大庆段工程的设计、施工提供科学依据.