山丘平原过渡区土壤重金属污染特征及评价——以四川省五通桥区为例

采集和分析了五通桥区不同功能区和乡镇73个土壤样品，以了解山丘平原过渡区土壤重金属的含量和污染特征。结果表明，重金属的平均含量为Pb32．18mg／kg、Cd0．82mg／kg、Cu28．61mg／kg、Zn108．08mg／kg、Ni32．66mg／kg、Cr72．44mg／kg；与四川土壤背景值相比，Cu、Ni、Cr的含量与之持平，Pb增加了0．11倍，Zn增加了0．32倍，Cd的积累较为严重，比背景值增加了10倍。污染评价结果显示该过渡区存在一定程度的重金属污染问题，不同功能区的污染程度排序为工业区〉生活区〉农业区。Cd在六种元素的土壤污染分担率中占55．46％，是最主要的污染元素；土壤Cd含量与Pb和Zn存在较高的相关性（相关系数为0．525和0．500），表明存在Pb—Cd和Zn—Cd的复合污染。     

Petrology, geochemistry and the mechanisms determining the distribution of platinum-group element and base metal sulphide mineralisation in the Platreef at Overysel, northern Bushveld Complex, South Africa

Platinum-group element (PGE) mineralisation within the Platreef at Overysel is controlled by the presence of base metal sulphides (BMS). The floor rocks at Overysel are Archean basement gneisses, and unlike other localities along the strike of the Platreef where the floor is comprised of Transvaal Supergroup sediments, the intimate PGE–BMS relationship holds strong into the footwall rocks. Decoupling of PGE from BMS is rare and the BMS and platinum-group mineral assemblages in the Platreef and the footwall are almost identical. There is minimal overprinting by hydrothermal fluids; therefore, the mineralisation style present at Overysel may represent the most ‘primary’ style of Platreef mineralisation preserved anywhere along the strike. Chondrite-normalised PGE profiles reveal a progressive fractionation of the PGE with depth into the footwall, with Ir, Ru and Rh dramatically depleted with depth compared to Pt, Pd and Au. This feature is not observed at Sandsloot and Zwartfontein, to the south of Overysel, where the footwall rocks are carbonates. There is evidence from rare earth element abundances and the amount of interstitial quartz towards the base of the Platreef pyroxenites that contamination by a felsic melt derived from partial melting of the gneissic footwall has taken place. Textural evidence in the gneisses suggests that a sulphide liquid percolated down into the footwall through a permeable, inter-granular network that was produced by partial melting around grain boundaries in the gneisses that was induced by the intrusion of the Platreef magma. PGE were originally concentrated within a sulphide liquid in the Platreef magma, and the crystallisation of monosulphide solid solution from the sulphide liquid removed the majority of the IPGE and Rh from it whilst still within the mafic Platreef. Transport of PGE into the gneisses, via downward migration of the residual sulphide liquid, fractionated out the remaining IPGE and Rh in the upper parts of the gneisses leaving a ‘slick’ of disseminated sulphides in the gneiss, with the residual liquid becoming progressively more depleted in these elements relative to Pt, Pd and Au. Highly sulphide-rich zones with massive sulphides formed where ponding of the sulphide liquid occurred due to permeability contrasts in the footwall. This study highlights the fact that there is a fundamental floor rock control on the mechanism of distribution of PGE from the Platreef into the footwall rocks. Where the floor rocks are sediments, fluid activity related to metamorphism, assimilation and later serpentinisation has decoupled PGE from BMS in places, and transport of PGE into the footwall is via hydrothermal fluids. In contrast, where the floor is comprised of anhydrous gneiss, such as at Overysel, there is limited fluid activity and PGE behaviour is controlled by the behaviour of sulphide liquids, producing an intimate PGE–BMS association. Xenoliths and irregular bands of chromitite within the Platreef are described in detail for the first time. These are rich in the IPGE and Rh, and evidence from laurite inclusions indicates they must have crystallised from a PGE-saturated magma. The disturbed and xenolithic nature of the chromitites would suggest they are rip-up clasts, either disturbed by later pulses of Platreef magma in a multi-phase emplacement or transported into the Platreef from a pre-existing source in a deeper staging chamber or conduit.     

The Removal of Dissolved Metals by Hydroxysulphate Precipitates during Oxidation and Neutralization of Acid Mine Waters, Iberian Pyrite Belt

This study examines the removal of dissolved metals during the oxidation and neutralization of five acid mine drainage (AMD) waters from La Zarza, Lomero, Esperanza, Corta Atalaya and Poderosa mines (Iberian Pyrite Belt, Huelva, Spain). These waters were selected to cover the spectrum of pH (2.2–3.5) and chemical composition (e.g., 319–2,103 mg/L Fe; 2.85–33.3 g/L SO₄⁼) of the IPB mine waters. The experiments were conducted in the laboratory to simulate the geochemical evolution previously recognized in the field. This evolution includes two stages: (1) oxidation of dissolved Fe(II) followed by hydrolysis and precipitation of Fe(III), and (2) progressive pH increase during mixing with fresh waters. Fe(III) precipitates at pH < 3.5 (stages 1 and 2) in the form of schwertmannite, whereas Al precipitates during stage 2 at pH 5.0 in the form of several hydroxysulphates of variable composition (hydrobasaluminite, basaluminite, aluminite). During these stages, trace elements are totally or partially sorbed and/or coprecipitated at different rates depending basically on pH, as well as on the activity of the SO₄⁼ anion (which determines the speciation of metals). The general trend for the metals which are chiefly present as aqueous free cations (Pb²⁺, Zn²⁺, Cu²⁺, Cd²⁺, Mn²⁺, Co²⁺, Ni²⁺) is a progressive sorption at increasing pH. On the other hand, As and V (mainly present as anionic species) are completely scavenged during the oxidation stage at pH < 3.5. In waters with high activities (> 10⁻¹) of the SO ₄⁼ ion, some elements like Al, Zn, Cd, Pb and U can also form anionic bisulphate complexes and be significantly sorbed at pH < 5. The removal rates at pH 7.0 range from around 100% for As, V, Cu and U, and 60–80% for Pb, to less than 20% for Zn, Co, Ni and Mn. These processes of metal removal represent a significant mechanism of natural attenuation in the IPB.     

探测地雷技术研究综述

高敏感度、高可靠度、低花费传感器是全自动或半自动探雷机器人的首要和绝对的选择。当前,有许多技术能够被选来综合使用以满足上述的要求。金属探测器是一种传统的、成熟可靠的探测技术。但是,现在多种地雷含有少量的金属或者不包含任何金属,造成了用金属探测器探雷的困难。目前迫切需要研究发展新颖的探测技术以消除100万颗地雷对许多国家的影响。     

自适应网格技术在MM5中的应用研究

结合一次暴雨过程，将自适应网格技术应用于中尺度模式MM5中进行数值试验，同时对比自适应网格方案和固定网格方案的优劣，对模拟结果作了诊断分析。结果表明：对于此次降水过程，自适应网格模拟的效果取决于一些参数的选择。     

长江下游一次大暴雨的中尺度模拟分析

运用中尺度数值模式（MM5V3.6）对2004年6月25日长江下游地区一次大暴雨天气过程进行了数值模拟,结合天气形势和卫星云图对此次过程进行了分析.结果表明：在东北冷涡和西太平洋副热带高压两大天气尺度系统的作用下,西南低空急流的再次加强和中低层切变线共同作用是此次大暴雨过程的主要原因.螺旋度分析表明,在不均匀的强上升气流的作用下,涡旋的水平分量向垂直分量转化是此次强降水的可能机制之一.     

一次诱发山地灾害突发性暴雨数值模拟及诊断分析

应用MM5V3.5中尺度非静力数值模式对2003年7月14～15日发生在陕西省一次区域性暴雨过程进行数值模拟和诊断分析,结果发现,西太平洋副热带高压西侧的暖湿气流和新疆冷空气是这次暴雨的主要影响系统,充沛的水汽输送、能量的积聚和强烈的上升运动为暴雨的发生提供了充分的条件,700hPa低涡、切变线是暴雨形成的触发机制.模拟结果表明：涡度场和散度场及垂直上升运动互耦;特强辐合辐散柱的出现早于强涡度柱,而深厚的强气旋性涡柱则几乎与暴雨最强盛时期同时出现.     

一次秋季局地强降水过程分析

对常规气象要素、卫星云图和T106物理量诊断产品进行分析,得出2001年10月2～3日发生在桂东南局地强降水成因及中尺度系统特征。     

南疆西部山区一次特大暴雨特征分析

通过对2001年9月22－23日南疆西北部山区特大暴雨的环流背景、物理量场、卫星云图分析，揭示了这场特大暴雨的物理机制和各要素场特征。     

1999年杭嘉湖平原一次连续暴雨过程诊断分析

用新的曲面拟合法(NMOCSF)对江淮和杭嘉湖平原一次连续暴雨过程作物理诊断，结合天气形势讨论了准静止华北高压的形成及其对江淮和杭嘉湖平原连续暴雨的贡献。指出，当江淮和杭嘉湖平原处在梅雨期时，应特别注意华北高压的强度和位置，一旦构成阻塞形势，就极可能发生大范围、持续性的强降水过程。