现阶段地表油气化探技术难题与发展对策

虽然地表油气化探方法技术已取得显著的应用效果, 但是由于成功率计算标准不同及方法技术本身的缺陷, 导致人们对方法的认同度较低。当前, 地表油气化探技术的发展, 一方面要以可靠的实验依据、严谨的数理推导及理论模型应对来自方法技术本身的挑战, 另一方面也要利用其快速、廉价和直接的优势, 加强与地质、遥感、非震物探等方法综合应用。     

地球化学异常再现性与可对比性

不同密度采样是否可以获得稳定的和可追索的地球化学模式是检验采样是否具有代表性，分析技术是否成熟的重要依据。笔者选择新疆哈密大南湖地区约6400km^2面积，进行了从超低密度(1个样／100km^2)，甚低密度(1个样／25km^2)直到低密度(1个样／4km^2)地球化学采样，对比了3种密度地球化学采样所获得的地球化学数据和异常分布模式。得出如下结论：超低密度、甚低密度、低密度地球化学调查获得的元素含量平均值和背景值非常接近；超低密度、甚低密度、低密度调查所圈定的地球化学省在形态上和变化趋势上非常相似，浓集中心的位置重合，表明不同调查阶段可获得稳定的和可追索的地球化学模式；采样密度越大数据离散程度越高，即最小值更小，最大值更大，表明元素分布的局部不均匀性，正是这种局部的不均匀性才能通过加密采样刻画出地球化学模式的细节变化，为逐步追踪矿化体奠定了基础；超低密度和甚低密度采样可以有效圈定矿集区所形成的大规模地球化学异常，低密度地球化学调查不仅可以圈定矿集区异常，同时可以圈定分散矿化的小规模局部异常。     

西昆仑山东段库牙克断裂与康西瓦断裂、阿尔金断裂关系的地球化学证据

新疆昆仑山中部库牙克地区，处于不同大地构造单元的结合部位，一些重要构造线均交会于此，确定它们之间的关系，关键在于库牙克断裂。1：20万区域化探最新成果显示，库牙克地区绝大多数元素两分性特征突出、南北差异明显，北部整体富集MgO、K2O、Na2O、Al2O3、CaO、Cr、Ni、Co、V、Ti、Au、La、Be，而贫Hg、As、Sb、B、Li，南部正好相反。两者之间的分界线从东向西依次对应于阿尔金断裂西段、库牙克断裂、阿什库勒断裂和康西瓦断裂东端。因此，从地球化学角度对库牙克断裂的延伸进行了推断，提出库牙克断裂东连阿尔金、西经阿什库勒与康西瓦断裂相接的新认识。     

热液矿床成矿元素地球化学异常探讨

为什么有些热液矿床矿体周围蚀变岩中出现明显的成矿元素负异常，而有些热液矿床矿体周围蚀变岩中出现明显的成矿元素正异常？以湘中地区锑（金）矿床为例，探讨了热液矿床成矿元素异常的形成机理，研究表明，热液矿床成矿物质来源的差异是导致成矿元素正异常或负异常的根本原因。     

非常规综合物化探油气预测研究

非常规综合物化探方法油气预测研究中存在的主要问题为：缺乏系统与综合的基础性理论研究，异常形成的机理还不十分清楚，在参数的优化组合及异常的求取上尚有诸多不足。针对后一种情况，选择松辽盆地东岭构造作为实验区进行了有益的探索。选取低能吸附烃、放射性测氡及土壤热释光三类参数进行了优化组合，分别计算了综合指标MAE与MAC及组合熵，然后对各值采用泛克里格法求取异常，取得了良好的效果。下一步研究应从异常形成的机理入手，建立三维非常规综合物化探油气预测模式，以提高油气预测成功率。     

熊耳山地区太古宙超镁铁质岩的地球化学特征及成因探讨

熊耳山地区太古宙超镁铁质岩在空间分布上具有不均一性、成带性和多方向性特征 ,岩石以橄榄岩、辉石岩、角闪石岩为主 ,蚀变强烈。岩石贫钙、镁 ,低铝、K2 O Na2 O,稀土总量较高 ,轻重稀土分馏显著。地球化学特征表明大部分超镁铁质岩体为岩浆侵入成因     

川滇黔桂76种元素地球化学图编制中分析方法与分析质量研究(一) 不同实验室产生地球化学图的相似性——以Ag、Cs、Ga、Ge为例

编制中国76种元素地球化学图将使我们首次了解元素周期表上除氢、氧及惰性气体之外所有元素在中国大陆表层的分布,川滇黔桂76种元素地球化学图的编制是这一研究项目的试点。本文以不同实验室取得的Ag、Cs、Ga、Ge分析数据为例,探索、衡量不同实验室地球化学图相似性的方法,以优选实验室进行川滇黔桂4省区约4000件组合样76种元素的大规模分析工作。     

Hydrothermal Redistribution of Rare—Earth Elements in Pingxiang Dacite,Guangxi

Distribution of the rare-earth elements (REE) in dacite has been studied so as to get a better understanding of the migration behavior of REE during alteration. Both unaltered and altered samples were collected in an unpolluted area of Guangxi Zhuang Autonomous Region, southwest China. The REE concentrations were analyzed by ICP-MS. It is concluded that the REE were enriched during dacite alteration in varying degrees. The chondrite-normalized REE patterns of altered samples approximately maintain the characteristics of unaltered samples. However, if we normalize the REE concentrations of altered samples with unaltered dacite, fractionation of REE will appear. The LREE are more enriched than HREE in all altered samples with the LREE possibly precipitated as carbonate minerals. Both positive and negative Eu anomalies exist. Enrichment, immobility and depletion are noticed for the element Lu. Heavy mineral alteration, difference in stability constant between carbonate LREE and HREE complexes, downward migration of weathering fluid and microenvironment change may be responsible for the fractionation of REE in the altered dacite.     

Fitness-for-Purpose of Reference Material Reference Values in Relation to Traceability of Measurement, as Illustrated by USGS BCR-1, NIST SRM 610 and IAEA NBS28

As in all fields of sample analysis, reference materials play a large role in supporting measurements in the geosciences. While a rather large number of materials are in distribution (> 380), not all are equally effective or fit-for-purpose in supporting laboratory data quality and thereby assuring the desired comparability of measurements between laboratories. Equally important, reference values that are not fit-for-purpose cannot be used effectively to establish traceability links between laboratory measurements and national and international standards. The needed fitness-for-purpose is not achieved for reference values either when more than one reference value has been proposed and a consensus does not exist among users as to which should be used by all, or when reference value uncertainties are too large in comparison to those of routine laboratory measurements. The focus of this review will be, first to outline the current reality, and second to suggest ways in which certifications of RMs can be improved to provide reference values that are universally accepted and more fit-for-purpose in general laboratory use. The discussion will be illustrated largely by current uses of USGS BCR-1, NIST SRM 610 and IAEA NBS28, as these three materials are those for which the largest body of newly published data exists, according to recent bibliographies of the geoanalytical literature published annually in Geostandards Newsletter: The Journal of Geostandards and Geoanalysis.     

Gold Mineralization and Occurrence of Sinter in the Hoshino Area, Fukuoka Prefecture, Japan

Abstract. Several epithermal gold deposits occur in the Hoshino area, which is located in the western end of the late Cenozoic Hohi volcanic zone, north‐central Kyushu, Japan. The area is characterized by intermediate to felsic extrusive rocks of Pliocene age. In the Hoshino area, the shallow manifestation of the hydrothermal activity is exposed on the surface. Several outcrops of sinter are still preserved on the top of hydro thermally altered volcanic rocks, and high‐grade gold‐bearing quartz veins occur on the surface at lower levels. The hydrothermal alteration resulted into well‐developed alteration zones. The zonal alteration pattern, primarily of near‐neutral pH type, is characterized by the outer smectite zone of a lower temperature, and the inner mixed layer minerals zone of a higher temperature. Quartz vein‐related or fracture‐controlled alteration, is represented by the occurrence of interstratified illite/smectite and K‐feldspar, suggesting a potassium‐enriched alteration. The mineralization in the Hoshino area is recognized on the surface by the occurrence of gold‐bearing quartz veins distributed mainly in the mixed layer minerals zone. The fracture system related to the gold mineralization is mainly characterized by NW‐SE trend. The alteration pattern and the mineralogical composition of the veins suggest that the mineralizing fluids had near‐neutral pH and the mineralization is of low‐sulfidation‐type. Fluid inclusion data and textures observed in quartz veins indicate that gold precipitated during boiling. The chemical composition of quartz veins shows that high‐grade gold‐bearing quartz veins are characterized by higher content of Al₂O₃, K₂O and Rb. Several outcrops of silica‐sinters are distributed on the top of the mixed layer minerals zone. Although their structures are not very well preserved, because of later silicification, the Hoshino sinters still show characteristic textures identical to those observed in modern sinters, such as the presence of plant fossil incorporated into the sinters, the strongly developed depositional laminations and the columnar structures perpendicular to the depositional surfaces. Quartz is the only silica mineral constituting the Hoshino sinters presently. The conversion of amorphous silica into quartz was probably governed by higher temperatures resulting from later hydrothermal activity. This later hydrothermal activity is reflected by the intense silicification affecting mainly the lower parts of the sinters and also by the presence of quartz veins cutting the sinters. The distribution of sinters in the Hoshino area is very significant. The presence beneath the sinters of concealed high‐grade gold‐bearing quartz veins should be highly considered and exploration work is strongly suggested.