Tectonic Dynamic Metallization of Silver-GoldHydrothermal Fluids in Proterozoic GneissTerrene Shear Zones, Suichang, Zhejiang, China

-,The well-known Suichang silvengold field is located inZhejiang Province of SOutheast China. It is the largest silver-gold deposit associated with copper and zinc in the Cathaysianmetallogenic province.There are a series of silver-gold dePOsits in the shear zonesof Proterozoic gneiss terrene, Suichang region. The volcanicapparatus at Mesozoic has complicated rpineralization. Respectively, there are two pieces of understanding on the origin ofore-formigg nuid: (l ) metamorphic fluid (Lia…     

北部湾地震的动力学参数与应力场

从震源机制和动力学参数方面讨论了北部湾地震的震源应力场，结果表明，主震是在北东东向构造的作用下发生的，同时计算了动力学参数如破裂长度，地震矩，应力降，破裂面积和平均位错等，并探讨了非线性地震与较大余震的关系。     

随机地震动场激励下拱坝多点输入的抗震可靠度分析

本文首次将空间随机地震场输入用于拱坝随机振动分析之中，与拱坝三维动力学有限元法结合，完成了三维拱坝在空间随机地震动场作用下的随机振动分析方法及算法的研究，另外考虑动力和静力的叠加，提出了三维空间随机地震动场的拱坝抗震可靠度分析方法，最后编制了相应的程序，对小湾拱坝进行了抗震可靠度分析，并与随机变量的结果进行了比较。     

地震灾场的模拟与模拟控制问题研究（Ⅰ）地震灾场模拟

本文将离散事件系统仿真的方法引入到地震工程研究之中．在论述地震灾场模拟与离散事件系统仿真的共性与差异的基础上，以城市地震次生火灾的发生与扑救过程为背景，发展了场、时域复合仿真模型，提出了城市地震灾场的综合模拟算法．实例研究表明，本文建议的地震灾场模拟算法可以揭示复合型工程系统地震反应的一系列特征参数。     

澜沧-耿马等强震迁移活动与地电前兆场时空关系

研究1988年11月至1990年10月近2a时间内,在22°～36°N,98°～104°E地区连发性的5次6级以上迁移地震与地电前兆的时空关系。结果表明,这组连发性迁移强震发生之前,地电前兆在南北两地区观测到两个应力相对集中区。随着南部系统内应力不断向北调整,发生了多次强震。这组连发性的强震孕育,包括它们各自前兆场分布和发育,彼此并不是孤立的,而是彼此呼应的。     

1945－1995地磁场功率谱及其长期变化

本文根据最新修正的国际地磁参考场模型，研究了１９４５－１９９５地磁场中心偶极矩变化，地磁总场及其分量Ｘ、Ｙ、Ｚ的空间功率谱，地磁场长期变化谱的经向漂移和纬向漂移的功率谱和西向漂移速度。研究中发现最近５０年偶极矩仍在继续衰减，空间功率谱的变化也呈减小趋势。在经向谱的漂移中观察到１９７０年出现最小值，而在纬向漂移变化中１９７０年出现最大值，西向漂移速度的变化也在１９７０年出现最大值，这种现象正是１９７０年发生的地磁长期变化的突变，称作地磁＂Ｊｅｒｋ＂。     

太阳宇宙线高能电子能谱的形成

提出了一个太阳脉冲和经变耀斑中高能太阳宇宙线电子能谱的形成模型，探讨了高能电子通过日冕捕获区的库仑损失、轫致辐射和同步辐射等物理过程，首次研究了日冕等离子体尾场对太阳宇宙线电子的加速及其能谱的形成．所得结果和观测谱能很好地符合，从而较合理地阐明了脉冲耀斑和经变耀斑两类太阳宇宙线高能电子谱的结构．     

非单一电离层扰动场的台阵探测分析

真实的ＴＩＤ一类大尺度电离层扰动是非平稳和色散的，而且是统计非单一的．本文首先给出了描述这种真实扰动场的数学模型，进而导出了联系台阵探测可测量与扰动场传播参量的观测方程，在此基础上提出了求解观测方程的时频分析方法．这一台阵探测数据分析的新方法，既能分离出非单一电离层扰动场中各种准单一扰动成分，又能获得准单一扰动成分传播参量随时间的演变和随频率的色散．分析实例表明，本文方法分辨率好，精度高，结果可靠，是适用于ＴＩＤ一类大尺度电离层扰动台阵探测数据分析的有效方法．     

Processing of oxidised nitrogen compounds by passage through winter-time orographic cloud

Four case studies are described, from a three-site field experiment in October/November 1991 using the Great Dun Fell flow-through reactor hill cap cloud in rural Northern England. Measurements of total odd-nitrogen nitrogen oxides (NO _y ) made on either side of the hill, before and after the air flowed through the cloud, showed that 10 to 50% of the NO _y , called NO _z , was neither NO nor NO₂. This NO _z failed to exhibit a diurnal variation and was often higher after passage through cloud than before. No evidence of conversion of NO _z to NO₃ ^- in cloud was found. A simple box model of gas-phase chemistry in air before it reached the cloud, including scavenging of NO₃ and N₂O₅ by aerosol of surface area proportional to the NO₂ mixing ratio, shows that NO₃ and N₂O₅ may build up in the boundary layer by night only if stable stratification insulates the air from emissions of NO. This may explain the lack of evidence for N₂O₅ forming NO₃ ^- in cloud under well-mixed conditions in 1991, in contrast with observations under stably stratified conditions during previous experiments when evidence of N₂O₅ was found. Inside the cloud, some variations in the calculated total atmospheric loading of HNO₂ and the cloud liquid water content were related to each other. Also, indications of conversion of NO _x to NO _z were found. To explain these observations, scavenging of NO _x and HNO₂ by cloud droplets and/or aqueous-phase oxidation of NO₂ ^- by nitrate radicals are considered. When cloud acidity was being produced by aqueous-phase oxidation of NO _x or SO₂, NO₃ ^- which had entered the cloud as aerosol particles was liberated as HNO₃ vapour. When no aqueous-phase production of acidity was occurring, the reverse, conversion of scavenged HNO₃ to particulate NO₃ ^-, was observed.     

Natural and anthropogenic C2 to C6 hydrocarbons in the central-eastern Venezuelan atmosphere during the rainy season

The levels of low molecular weight hydrocarbons were measured at pristine sites and rural locations affected by hydrocarbon emissions from oil and gas producing fields in Venezuela. At the clean sites, lower concentrations of C₂ to C₆ alkanes were observed, whereas, in comparison with remotes sites, very much higher levels were measured at the polluted sites. Alkenes present relatively high concentrations, with isoprene being the most abundant, all over the study region. The main sources of alkenes are likely to be natural, mainly from vegetation. The levels of alkanes recorded at the clean sites and the alkene levels found everywhere in the region are in agreement with the values reported for other clean sites in the tropics. The increase of ozone production capacity due to the anthropogenic emissions of alkanes from oil and gas fields was estimated. Due to the presence in the atmosphere of important amounts of naturally emitted isoprene, ethene and propene, which makes a substantial contribution to the reactivity of the hydrocarbon mixture, a small increase (<5%) was estimated to occur in the capacity of the ozone production at a regional scale during the rainy season.