金在表生条件下溶解,迁移和沉淀的探讨

金矿物在表生条件下溶解为离子金.离子金与表生络合剂结合成金络离子团迁移.在物化条件改变时,由于有机炭、粘土矿物及带异性电荷胶体吸附,使金络离子团分解成原子金沉淀.     

1991年北半球夏季风及江淮流域降雨量的低频振荡

根据１９９１年５－８月江淮特大暴雨资料，使用功率谱和带通滤波结合的方法，研究了１９９１年夏季风和江淮梅雨的准周期振荡，探索季风对异常梅雨的影响。分析指出，１９９１年北半球夏季风活动，江淮流域湿度场和降雨量变化均存在显著的准２４天周期振荡，夏季风的周期振荡，主要表现在西南季风（东南季风不明显），它的位相比降雨量提前２－４左右，其振幅大小较好地反映了降雨量的大小。     

第四纪盐湖型钾盐矿床的航空γ能谱异常特征及找矿模式

本文以航空γ能谱测量资料为依据，简述了与找钾有关的部分科研成果，建立了第四纪盐湖型钾盐矿床的找矿模式，进而通过对别勒滩、马海等钾盐矿例剖析，说明航空γ能潜测量在寻找第四纪盐湖型钾盐矿床方面确有明显效果。     

极隙区粒子和电流的观测和研究

处于高纬向日面的极隙区是太阳风能量、动量和质量可以直接进入地球磁场并到达地球的近地空间的区域。本文简要介绍了极隙区的观测和研究，综述了极隙区的粒子沉降、场向电流、等离子体对流和电离层电流的特征。     

Lower Tropospheric Warm Air Advection Patterns Associated with Heavy Rainfall over the Appalachian Region*

A synoptic climatology of warm season heavy rainfall is developed from patterns of 850 mb thermal advection over the Appalachian region. Heavy rain events are categorized according to the position and orientation of a warm air advection (WAA) ridge, a feature found in nearly two-thirds of the events. Numerous study events occur within the conditionally unstable region of the WAA ridge. In fact, numerous occurrences of heavy rainfall are tied to a superpositioning of a WAA and air mass instability ridge in the vicinity or upstream of the heavy rain area.     

Symplectitic augite: evidence for discontinuous precipitation as an exsolution mechanism in Ca-rich clinopyroxene

Abstract Part of the augite in the Artfjället gabbro consists of symplectitic intergrowths between augite and blebs or lamellae of orthopyroxene. Mineral compositions are consistent with formation of these symplectites by exsolution of orthopyroxene from magmatic augite at a temperature of ca . 900–1000°C. The microstructures indicate that the exsolution mechanism is discontinuous precipitation, whereby the boundary of an augite grain sweeps through a neighbouring augite, leaving the symplectite in its wake. The formation of this symplectitic augite is catalysed by the presence of an intergranular water-rich fluid phase, which promotes grain boundary mobility.     

Nonequilibrium thermodynamics of pressure solution

This paper is concerned with the thermodynamic theory of solution and precipitation processes in wet crustal rocks and with the mechanism of steady pressure-solution slip in contact zones, such as grain-to-grain contacts, fracture surfaces, and permeable gouge layers, that are infiltrated by a mobile aqueous solution phase. A local dissipation jump condition at the phase boundary is fundamental to identifying the thermodynamic force driving the solution and precipitation process and is used here in setting up linear phenomenological relations to model near-equilibrium phase transformation kinetics. The local thermodynamic equilibrium of a stressed pure solid in contact with its melt or solution phase is governed by Gibbs's relation, which is rederived here, in a manner emphasizing its independence of constitutive assumptions for the solid while neglecting surface tension and diffusion in the solid. Fluid-infiltrated contact zones, such as those formed by rough surfaces, cannot generally be in thermodynamic equilibrium, especially during an ongoing process of pressure-solution slip, and the existing equilibrium formulations are incorrect in overlooking dissipative processes tending to eliminate fluctuations in superficial free energies due to stress concentrations near asperities, defects, or impurities. Steady pressure-solution slip is likely to exhibit a nonlinear dependence of slip rate on shear stress and effective normal stress, due to a dependence of the contact-zone state on the latter. Given that this dependence is negligible within some range, linear relations for pressure-solution slip can be derived for the limiting cases of diffusion-controlled and interface-reaction-controlled rates. A criterion for rate control by one of these mechanisms is set by the magnitude of the dimensionless quantityk/2C _pD, wherek is the interfacial transfer coefficient, is the mean diffusion path length,C _p is the solubility at pressurep, andD is the mass diffusivity.     

The Chemical Composition of Global Subducting Sediments and Its Geological Significance

Subducted sediments play an important role in crust-mantle interaction and deep mantle processes, especially for subduction zone magmatism and mantle geochemistry. The current rate of Global Subducting Sediments (GLOSS) is 0.5~0.7 km³/a. The GLOSS are composed of terrigenous material(76 wt.%), calcium carbonate(7 wt.%), opal(10 wt.%) and mineral-bound H₂O⁺(7 wt.%). The chemical compositions of GLOSS are similar to those of upper continental crust which is mainly controlled by the terrigenous materials, and yet the materials formed by marine processes will dilute the terrigenous materials. The components of subducted sediments are different among trenches. In the accretionary margin, the components of subducted sediments are similar to those of the upper crust, while in the non-accretionary margin the components are terrigenous materials plus those produced by marine processes. During subduction, subducted sediments will released fluids, melt or supercritical fluid to affect island arc/back-arc basin magmatism by means of aqueous fluid or sediment melt. In addition, a part of subducted sediments, together with underlying altered oceanic crust/lithosphere, recycle into the mantle and contribute to the mantle heterogeneity. Geochemical tracers indicate that subducted sediments play variable contributions to the magmatic processes in different tectonic setting. Thus, subducted sediments play an important role in two relatively independent dynamics systems (plate tectonics and mantle plume), as well as related mantle evolution models. As a result, by accurately calculating the compositions of subduction sediments and using various geochemical indicators, we can further limit the input and output fluxes of various elements or isotopes, and then obtain more accurately residual subducted components, which can provide us some important clues for geodynamic process.