早期矿业发展与地质学的诞生

石头是人类由蒙昧走向智慧的启蒙，彩石和矿物颜料开启了人类对美的认识和追求。人类在使用矿物岩石中相继出现的武器、农耕时代、陶器、金属冶炼、人类聚落和城邦，标志着人类智慧的爆发和文明根基的建立。遍布全球的规模性采掘和矿业活动为早期人类社会的发展奠定了工业和经济基础，给人类认识矿物岩石和探索地球的奥秘打开了大门。东西方先哲们最早观察和思索天地万物、物质组成和变化、探索石头和金属的形成，炼丹术和炼金术、早期博物学、早期医学对金属、矿物和岩石的进一步探索与实践，孕育了现代矿物学和地质学。中世纪矿业的繁荣带动了地质科学研究的复兴，矿床学和矿物学的确立、化石研究与地层层序的确立、岩石成因的水火之争、山脉成因的垂向升降和水平挤压之争导致了地质学的诞生和确立。     

中国南方离子吸附型稀土矿床成矿类型及其母岩控矿因素探讨

传统认为中国南方的离子吸附型稀土矿床可划分为以“足洞式”为代表的重稀土型和以“河岭式”(或“花山式”)为代表的轻稀土型两种矿化类型。然而，近年来发现的许多矿床(如清溪、寨背和馒头山等)的赋矿风化壳中出现了轻稀土矿与重稀土矿并存现象，表现出特殊的“上轻下重”双层矿体结构。这指示了除重稀土型和轻稀土型之外，还存在着轻重稀土共生型的过渡类型。本研究通过对三种不同成矿类型的若干典型矿床系统对比，指出成矿类型的多样性与母岩性质密切相关，尤其是母岩的稀土元素地球化学和稀土载体矿物属性是制约成矿类型变化的关键因素。统计数据表明，从重稀土型→轻重稀土共生型→轻稀土型，成矿母岩的全岩稀土总量变化不大(ΣREY: 200×10-6~450×10-6→200×10-6~500×10-6→200×10-6~800×10-6)，但轻重稀土配分值出现较显著的区间性差异(ΣLREE/ΣHREY: 02~1→1~5→2~10)。与之同时，母岩中能为离子相稀土提供物源且具有重稀土配分属性的稀土副矿物类型和数量明显减少，这与全岩稀土元素地球化学特征中重稀土分量占比的降低趋势也互相匹配。该结果指示，以往认为重稀土配分母岩形成重稀土矿床、轻稀土配分母岩形成轻稀土矿床的传统观点需要外延，即一部分具有低度轻稀土配分属性(1＜ΣLREE/ΣHREY＜5)且含有丰富易风化稀土副矿物的母岩还可能形成轻重稀土共生型矿床，该认识可为今后离子吸附型稀土矿床勘查工作提供新的找矿依据。     

高分遥感影像城市绿地自动提取方法

城市绿地作为城市生态系统中不可缺少的一部分,也是城市建设中必须考虑的因素之一,如何更有效地得到城市绿地的分布状况对城市的建设有着深刻的意义.高分辨率遥感影像如今已经成为城市绿地调查的重要数据.为了探究最适用于高分影像中城市绿地自动提取的方法,以南京市某区域为例,以高分二号高分辨率影像为数据源,分别使用了监督分类、利用归一化植被指数(NDVI)分类和基于规则的面向对象分类这三种信息自动提取方法,并将得到的分类结果与精度评价进行了对比分析,结果表明,基于规则的面向对象分类方法的精度明显高于其他两种方法.     

参数的期望估计及其在形变分析中的应用

利用“参数的期望估计”能准确定位、定量粗差及参数的期望估计不受粗差影响折特殊性质,寻找地壳变形区域和不变形区域,以确定拟稳点,进而进行拟稳变换,分析地菜变,将是一种有效方法。     

重视和加强岩矿物性的测量研究

本文从物探科学技术的进步,勘查任务的发展变化、物探方法应用范畴的扩大和物性勘探等几个方面,论述了岩石和矿物物理性质测量、研究的重要性,指出：物性工作不可能毕其功于一役,并提出了五点建议：１．深入研究各类矿藏及其围岩（直至地面）物性的空间变化规律,为选择、研究合适的物探方法,提高物探效果,进一步探讨“直接”找矿问题,提供依据;２．这项工作可专门进行,但最好尽可能利用为其他目的而设计的钻井进行;３．物     

湘中“桃江式”锰矿含锰岩系的定量研究及其找矿意义

本文从分析地质体数学特征的思想出发,来研究“桃江式”锰矿的含矿母岩－“含锰岩系”的数学特征。含锰岩系主要由五种岩石组成：粘土岩、黑色页岩、条带状页岩、含锰灰岩和碳酸锰矿层,其数学特征研究包括其统计特征分析、结构特征分析和空间特征分析。文最后讨论了这些数学特征在寻找同类锰矿中的意义。     

基于GIS的TM数据分类及辅助制图研究

本文初步研究了遥感、GIS和制图一体化实用技术方法。对黄土丘陵区和沙漠地区TM数据进行了特征信息分析;给出了分层分类和GIS辅助分类结果;经模糊推理和人机交互修改,将提“纯”的遥感专题数据作为GIS的动态信息源,对GIS进行扩充与更新;最后在GIS支持下分层提取专题图并进行辅助制图。     

Catalytic ozonation of phenol in water with natural brucite and magnesia

Catalytic ozonation has attracted much attention in treatment of wastewater for its mild conditions. Phenol and its ramifications are common components in a wide variety of wastewaters including those from coal conversion processes, coking plants, petroleum refineries and several chemical industries. In this paper, natural brucite and magnesia have been successfully used in catalytic ozonation of phenol. And the mechanisms of catalysis were also investigated. From Figs. 1 and 2, it can be found that both brucite and magnesia have remarkable catalysis on degradation of phenol and removal of Chemical Oxygen Demand （COD）. The pH of solutions on the process of ozonation alone, catalytic ozonation with brucites and with magnesia were 6.35-2.76, 10.18-8.52 and 10.58-10.83, respectively. It can be concluded that alkali environment plays a critical role for catalytic ozonation of phenol. We also found that the alkaline minerals reacted on the surface with oxalic acid and other low molecular-weight acids which are intermediate products in ozonation, but those intermediate products could be mineralized into carbon dioxide completely with enough ozonation time.     

Hydrogeochemical controls on surface and groundwater chemistry in naturally acidic, porphyry-related mineralized areas, southern Rocky Mountains

In southern Rocky Mountains, catchments characterized by acidic, metalliferous waters that are relatively unaffected by human activity usually occur within areas that have active or historical mining activity. The US Geological Survey has utilized these mineralized but unmined catchments to constrain geochemical processes that control the surface- and ground-water chemistry associated with near surface acid weathering as well as to estimate premining conditions. Study areas include the upper Animas River watershed, Lake City, Mt. Emmons, and Montezuma in Colorado and Questa in New Mexico. Although host-rock lithologies range from Precambrian gneisses to Cretaceous sedimentary units to Tertiary volcanic complexes, mineralization is Tertiary in age and associated with intermediate to felsic composition, porphyritic plutons. Pyrite is ubiquitous. Variability of metal concentrations in water is caused by two main factors： mineralogy and hydrology. Parameters that potentially affect water chemistry include： host-rock lithology, intensity of hydrothermal alteration, sulfide mineralogy and chemistry, gangue mineralogy, length of flow path, precipitation, evaporation, and redox conditions. Springs and headwater streams have pH values as low as 2.5, sulfate up to 3700 mg/L and high dissolved metal concentrations （for example： Al up to 170 mg/L; Fe up to 250 mg/L; Cu up to 3.5 mg/L and Zn up to 14 mg/L）. With the exception of evaporative waters, the lowest pH values and highest Fe and Al concentrations occur in water draining the most intense hydrothermally altered areas consisting of the mineral assemblage quartz-sericite-pyrite. Stream beds tend to be coated with iron floc, and some reaches are underlain by ferricrete. When iron-rich ground water interacts with oxygenated waters in the stream or hyporheic zone, ferrous iron is oxidized to ferric iron, which is less soluble, leading to the precipitation of iron oxyhydroxides.