The suitability of floodplain sediment as a global sampling medium: evidence from China

Research undertaken by IGCP 259 (International Geochemical Mapping) indicates that wide-spaced sampling is a fundamental concept of international geochemical mapping as it appears to provide the only practical way to obtain a relative rapid (10–20 years) overview of global geochemistry. The main aim of this study is to test the suitability of floodplain sediment as a global sampling medium.Thirteen floodplain sediment samples and 13 stream sediment samples were taken at the exit of 13 super large drainage basins (SCB). The areal extents of these basins are in the order of 1000–10,000 km². Within each SCB, 3–11 stream sediment samples each representing a component catchment basin (CCB) of 100–1000 km² were also taken. Fourty nine elements were analyzed. The results were compared with the average values derived from calculating thousands of stream sediment data available from China's National Geochemical Mapping (RGNG) program. Strong similiarities were demonstrated in distribution and trends among the three levels of data. The set of floodplain sediment data shows great coincidence with RGNR stream sediment data.     

Representativity of wide-spaced lower-layer overbank sediment geochemical sampling

To develop a technique of implementing global ultra-low density geochemical sampling and as a contribution to the International Geochemical Mapping Program (IGCP Project No. 259), an orientation study in the use of deep (lower-layer) overbank sediments was conducted in Jiangxi Province of Southeast China in 1989–1990. Ninety-four samples were collected at depths of 50 to 120 cm from overbank terraces at an average density of 1 site per 1800 km². The total area of sampled catchment basins is approximately equivalent to 18% of Jiangxi Province. Most of the samples were collected at outflow sites of catchment basins with areas of 100 to 800 km². The samples were analyzed for 39 elements.The representativity of wide-spaced lower-layer overbank sediment sampling is discussed from various perspectives; the following features have been observed: (1) Widespaced lower-layer overbank sediment data and the data from China's national geochemical mapping (RGNR) project show similar geochemical patterns for W, Sn, Pb, Cu and Zn. (2) The results of wide-spaced lower-layer overbank sediment sampling demonstrate that catchment basins with areas of 100 to 800 km² are suitable sample site locations for the global geochemical reference network. (3) Wide-spaced lower-layer overbank sediment sampling is a fast and cost-effective way to identify geochemical provinces and has strategic significance in mineral exploration. (4) There is a significant correlation between the W content of wide-spaced lower-layer overbank sediment samples and the presence of W mineralizations within the catchment basins. (5) The distributions of Ni, Cr and V in wide-spaced lower-layer overbank sediment samples distinctly reveals the boundary between the Yangtze sedimentary platform and the South China Caledonian fold system in Jiangxi Province. (6) Distributions of Rb and Be coincide with the Yanshan granites, which are closely related to the major ore-forming episodes in Jiangxi Province.     

Geochemistry of stream water in a catchment in Finland affected by sulphidic fine sediments

The impact of sediment type on stream water geochemistry was studied in a catchment in Finland affected by sulphidic fine-grained sediments. Stream water samples for general characterisation of water quality (pH, electrical conductivity) were taken at the basin outlet during various hydrological conditions, while samples for detailed geochemical analysis were collected at 119 sites in the catchment on one single occasion during high-water flow in autumn. The occurrence of sulphidic fine sediments was estimated based on data from an airborne electromagnetic survey carried out by the Geological Survey of Finland.Growing-symbol maps, which were prepared for each of the studied variables in water, and statistical calculations including factor analysis and Spearman correlations show that the concentrations of Al, Ga, U and Tl, all the lanthanides and several alkali and alkaline earth metals (K, Mg, Na, Li, Ca, Rb, Sr), transition metals (Cd, Co, Cu, Zn, Sc, Mn, Ni, Y, Hf) and non-metals (S, Br, I, Si) increase in water when the proportion of the catchment cover of sulphidic fine sediments increases. It is therefore argued that these elements are released and mobilised in considerable amounts by the oxidation and subsequent acidification and weathering of this type of sediment. Other elements are either slightly depleted in streams in areas of sulphidic fine sediments (V, Nb, Pb, Zr), have a distribution unrelated to sediment type (Fe, Cr, Cs, Mo), or are only weakly impacted by the occurrence of sulphidic sediments in the catchment (As, Ti, Ba). It is argued that these elements are not leached extensively from the oxidising sulphidic sediments, and that their distributions at least partly may be controlled by the contents of dissolved humic material and/or suspended organic and inorganic phases in the water.     

A catchment basin approach to the analysis of reconnaissance geochemical-geological data from Albay Province,Philippines

A systematic approach for identifying mineral exploration target areas from reconnaissance stream sediment data without sufficient a-priori control information has been demonstrated in a portion of western Albay Province in the southern Bicol Peninsula of the Philippines. The approach involved devising a rapid method of catchment basin mapping using a geographic information system (GIS) so that the areal influence of the catchment basins may be incorporated in the geochemical data analysis. Areal proportions of mapped rock units occurring in the sample catchment basins and observed Mn and Fe contents in stream sediments are used as independent variables in multiple regression analysis to predict element contents in stream sediments related to lithologic and chemical controls. The predicted element contents are filtered-out from the original data to leave residuals in which the effects of other factors (e.g., mineralization) may be seen. A simple correction for the effects of downstream dilution is applied; this allows for the different sizes of the sample catchment basins so that positive geochemical residuals are enhanced. The inter-relationship of the different positive residuals in ‘highly enriched’ samples are investigated through principal components analysis to determine and quantify an ‘anomalous geochemical signature’. Lastly, the ‘anomalous geochemical signature’ is integrated with ‘proximity’ to faults/fractures to determine favourable target areas. For the test region, the lithologic controls explain between 80% and 100% of the variability in most of the elements studied. Chemical controls account for generally less than 5% of the variability in the data. Most of the dilution-corrected residuals reveal high relative enrichment in certain areas underlain by andesite and/or diorite. An anomalous Cu-Mg-Fe-Zn geochemical signature is disclosed by the principal components analysis of the dilution-corrected residuals in ‘highly enriched’ samples. Most sample catchment basins defined by this ‘anomalous geochemical signature’ pertain to areas underlain by andesitic rocks. Integration of the ‘anomalous geochemical signature’ and ‘proximity’ to faults/fractures reveals that some of these anomalous sample catchment basins are favourable target areas. These areas are interpreted to contain andesite-hosted stockwork or stringer zones that once formed part of a complete stratigraphic sequence of a volcanogenic massive sulphide occurrence. The results demonstrate the usefulness and ability of the procedures followed to extract significant anomalies from the reconnaissance geochemical data without the benefit of sufficient a-priori control data to aid in anomaly recognition. Similar procedures could also be applied elsewhere.     

Assessment of trace metals contamination in stream sediments and soils in Abuja leather mining,southwestern Nigeria

This study is aimed at determining the level of environmental degradation as well as the concentration of trace elements in soil and stream sediments in order to evaluate the environmental impact of the mining operation. Twenty-five (25) soils and ten (10) stream sediment samples were collected from the study area. The physicochemical parameters were determined using appropriate instrumentation with the aid of a digital pH meter (Milwaukee meter) to measure the pH and electrical conductivity, total dissolved solids, moisture content and loss on ignition of the soil and stream sediment samples. The pH of the soil sample ranged from (6.10 to 7.19); Electrical conductivity ranged from (21.3 to 279.4 µS/cm), moisture content varied from (0.60% to 7.20%), and the LOI ranged from (2.03% to 18.62%). The results of the analysis showed that the concentrations of the trace elements in the soils and stream sediment samples were slightly higher than the background values. Plots of the trace elements in stream sediment samples show moderate, consistent decrease downstream except at points where there was mine water discharge into the main river. The pollution levels of heavy metals were examined in stream sediment and soil samples using different assessable indices, such as the enrichment factor, which showed significant-moderate enrichment for Cr, Th, Nb, Zn, Pb, Y and Zr and the geo-accumulation index, which showed practically moderate contamination with Cr, Ni and Sr based on regional background reference values. Geo-accumulation index and contamination index for soils and stream sediment revealed uncontaminated to moderate contamination. Likewise, elements with moderate contamination were Cr, Ni and Sr. The Pearson correlation showed that there were significant positive associations among selected metals in soil and stream sediment samples.     

Gold enrichment characteristics and exploration prospects in Zambia: Based on 1∶1000000 geochemical mapping

The 1∶1000000 geochemical mapping of Zambia provides catchment sediment geochemical data for 58elements including Au from 746 sediment samples at 736 sampling sites,corresponding to a sampling density of about one site per 1000 km2.Under strict quality control using field duplicates,certified reference materials,and analytical replicate samples,the Au was determined by Inductively Coupled Plasma Mass Spectrometry(ICP-MS).The detection limit of Au was 0.20×10^-9.The 95%range(2.5%–97.5%)of Au concentrations was from 0.24×10^-9 to 1.36×10^-9,and the median value was 0.40×10^-9.The most noticeable Au distribution patterns shown on the map are mainly located between Lusaka and Ndola(Lufilian Arc Belt).In addition,several high Au value areas occurred in Mansa,Muyombe,Chipata,and Livingstone.The spatial distribution patterns of Au in tectonic units,drainage basins,and geomorphological landscapes could be related to the Lufilian Arc Belt and Bangweulu Block.The Au concentrations show metallogenic belts between Muyombe and Mbala areas,between Mansa and Ndola areas,and between Lusaka and Kasempa areas.     

依据化探成果对东昆仑地质背景的讨论

在东昆仑地区 6 0 0 0 0多km2 的地域内 ,按照 4km2 的采样单元 ,共采集了 15 0 0 0多件水系沉积物样品。按照 16km2 的网格加工成 4 0 0 0多件组合样后 ,定量分析了 4 0种微量元素的含量。在对这些数据进行数学处理的基础上 ,利用斜交因子的分析结果 ,讨论了东昆仑地区的区域地层、断裂构造和中酸性岩浆岩的特征。根据区域地球化学成果 ,进一步明确了昆中、昆南断裂对本区地层和侵入岩分布的控制作用。基于元素区域地球化学背景的对比 ,提出了昆中断裂应向东延伸的证据 ,并指出了东大滩、布青山两个地区经历了相似的地质 地球化学作用     

Introducing a new approach of geochemical anomaly intensity index (GAII) for increasing the probability of exploration of shear zone gold mineralization

Increasing the prediction rate in the identification of mineralization zones using the stream sediment geochemical data is an essential issue in the regional exploration stage. The various univariate (such as fractal and probability plot (PP) methods) and multivariate methods (such as principal component analysis (PCA)) have been performed for interpreting the geochemical data and detecting the mineralization areas. In this study, a new geochemical criterion named geochemical anomaly intensity index (GAII) was proposed for geochemical anomaly mapping. This approach was developed based on the PCA method and the catchment basin coefficient (CBC). The GAII as a weighted geochemical index is calculated using the mineralization principal component (MPC) scores and CBC. GAII can be mapped and utilized for geochemical anomaly mapping and detecting the mineralization areas. Besides, GAII can identify paragenesis elements better than the current methods. In this research, GAII was successfully used to generate geochemical anomaly maps on shear zone gold mineralization in the southwest of Saqqez, NW Iran. The geochemical data have been divided into three groups based on catchment basins and the host rock type. Then the MPCs and paragenesis elements of Au mineralization have been obtained individually using PCA. Three mineralization paragenesis groups consisting of (Au, Sn), (Au, W), and (Au, As, Sb and Ba) have been recognized for different catchment basins of the southwest of Saqqez district using PCA. GAII was calculated and mapped based on the CBC_{(Au, Sn)}, CBC_{(Au, W)}, CBC_{(Au, As, Sb, Ba)}, and their MPC scores. GAII accurately detected the Au mineralization zones and improved the geochemical anomaly map in this area compared to the PP method, concentration-area fractal model, and U-spatial statistics method. The results demonstrated that GAII was successfully used for (a) identifying the mineralization paragenesis elements, (b) intensifying the geochemical anomaly, and (c) increasing the prediction rate of mineralization zones. The shear zone gold mineralization areas in the southwest of Saqqez district were effectively detected using this new data analysis approach. GAII has provided better results than the current PP method, concentration-area fractal model, and U-spatial statistics method.     

Calcium distribution in soils and stream sediments in Istria (Croatia) and the Slovenian littoral

For experimental geochemical mapping soil was sampled in 5×5 km regular grid in Istria and the Slovenian littoral (Croatia and Slovenia). The territory consists predominantly of karstified limestones and dolomites, and of flysch beds exposed in two basins, Istrian and Brkini. In addition to soil, stream sediment was also collected in the flysh area. Sampling was performed according to an analysis of variance design that permitted one to estimate the effects of the sample medium, geographic position, sampling error and analytical error. The analysis of variance of chemical variables indicated that soil and stream sediment as sampling media lead to similar results in producing geochemical maps. The largest differences with respect to the lithologic substrate of soil is indicated by calcium. As shown by the geochemical map, calcium in soil is high on the Istrian flysch beds, and low on limestones as well as on the flysch beds of the Brkini basin. The two soils also differ in mineralogy. The reason for this difference seems to lie in soil genesis on limestone and on flysch, and in the variable calcium content of flysch beds. The results of Q-mode factor analysis confirmed the adherence of soil and stream sediment of the two flysch basins to two differing groups. This difference was discovered by geochemical mapping. The hypothesis of differing calcium content in the rocks of the two basins was confirmed by the investigation of fresh and weathered rocks and soils in eight profiles sampled in the Brkini and Istrian flysch basin. It was found that the sandstone and calcarenitic samples from the Istrian basin contain an average factor of 3.5 more Ca than those of the investigated Brkini basin, and the samples of Istrian marls 4 times more Ca than those of the Brkini siltstones. Furthermore, the investigated weathered rocks and soils that originated from these rocks in the Istrian basin contain considerably more Ca than in the Brkini basin. In comparison with sandstone and siltstone samples of the Brkini basin, sandstone, calcarenite and marl samples of the Istrian flysch basin contain less clay minerals, quartz and feldspars and more calcite.     

A comparison of regional geochemical data from lakes and streams in northern Labrador; implications for mixed-media geochemical mapping

Labrador has been covered by reconnaissance-scale geochemical surveys under the National Geochemical Reconnaissance program. Lake sediment and water were the chief sample media, but stream sediment and water were employed in the mountainous terrain of northern Labrador. The main objective of these surveys was mineral resource assessment, but the data are also relevant to geological and environmental studies, and would be most useful to the non-specialist if the data from the two drainage types could be combined to produce unified element distribution maps for the whole region.A comparison of stream and lake data for a 5,700-km² area where both drainage types were sampled suggests that only the pH of the lake and stream waters are directly comparable, showing a common range and similar spatial distribution. Comparing the two types of sediment, most elements show obvious differences in either median content or range or both, indicating that stream and lake sediment are geochemically distinct media, and their element contents cannot be compared directly. The distribution patterns of Cu, Ni and U reflect similar bedrock features in both sediment types. In contrast, Co, F, Fe, Hg, Mn, V and Zn show little or no spatial correlation between stream and lake sediment, but are strongly intercorrelated in the stream sediment data set.The sediments collected from lakes in Labrador represent disturbed column, about 40 cm in length, of organic debris that accumulated over the past several hundred years. Metal accumulation in the sediment is largely through fixation from inflowing surface and groundwater by microorganisms, coprecipitation with hydrous Fe and Mn oxides, sorption by clay minerals and chemical and biochemical processes at and just below the sediment/water interface. The stream sediments in this study were collected from active sediment, and represent principally the mechanical-weathering products of bedrock, with variable amounts of organic matter and hydrous Fe and Mn oxides. Considering the difference in the two sediment types, it is probably not surprising that there is rather limited spatial correlation between the geochemistry of the two sediment types indicating that to a large extent each medium reflects a different facet of the bedrock geochemistry. Only for a few elements should the data sets be merged. The degree of spatial correlation for U, Ni and Cu increases as the data are generalized by averaging into larger blocks, suggesting that the combined data sets will be more successful in defining broad crustal geochemical features rather than local details. The implication of this study for international geochemical mapping is that geochemical patterns for many elements are strongly dependent on the sample medium chosen. Therefore, when it is necessary to change sample media in passing from one terrain type to another, a comparative study must be carried out to determine how the geochemistry of the different sample media compare spatially.     

High resolution regional hydrogeochemical baseline mapping of stream water of Wales,the Welsh borders and West Midlands region

The stream water hydrogeochemical database, produced by the Geochemical Baseline Survey (GBASE) of the British Geological Survey, has recently been enhanced in the light of experimental pilot studies in North Wales, to meet a wider range of economic and environmental objectives which require modern, integrated and strategic geochemical surveys for their implementation. Hydrogeochemical data are therefore now collected, in conjunction with geochemical data for stream sediments, soil samples and mineral concentrates. The density of sampling, based on the collection of stream water at near-baseflow conditions during the late summer period each year, has been increased to one site per 1.75 km² and a broader spectrum of geochemical determinants introduced. Provisional regional datasets are being prepared for an extensive region covering Wales, the Welsh Borders, and part of the West Midlands representing over 17 000 sample sites. Bedrock geology and base metal sulphide mineralisation are particularly well reflected in the stream water chemistry at the regional scale. The influence of secondary factors, such as geomorphology, atmospheric controls, and anthropogenic contamination due to agriculture, urban, industrial and military developments, can also be readily distinguished.The data obtained by systematic high resolution sampling of first and second order streams, vary in concentration over three or four orders of magnitude for many of the analytes studied here. This compares with a range of only one or two orders of magnitude for many of the analytes in stream sediment samples. The extended range in values for stream water is an important factor in the gridding, plotting and production of relatively stable maps. They are relatively unaffected either by short temporal changes in stream water flow, which are attributable either to storm events noted during the sampling campaign, or by annual differences between wet and dry summers in different years. This has enabled a series of robust surface hydrogeochemical maps to be prepared for analytical data collected during the summer sampling campaigns conducted annually from 1989 to 1994. These maps provide a unique source of synoptic baseline information for a wide range of economic and environmental applications especially, when combined with other geoscience datasets in a GIS environment.     

Geochemical mapping using stream sediments in west-central Nigeria: Implications for environmental studies and mineral exploration in West Africa

This paper provides an overview of regional geochemical mapping using stream sediments from central and south-western Nigeria. A total of 1569 stream sediment samples were collected and 54 major and trace elements determined by ICP-MS and Au, Pd and Pt by fire assay. Multivariate statistical techniques (e.g., correlation analysis and principal factor analysis) were used to explore the data, following appropriate data transformation, to understand the data structure, investigate underlying processes controlling spatial geochemical variability and identify element associations. Major geochemical variations are controlled by source geology and provenance, as well as chemical weathering and winnowing processes, more subtle variations are a result of land use and contamination from anthropogenic activity.     

贵州西部龙场地区水系沉积物Pt、Pd异常源地球化学示踪的初步研究

以贵州龙场地区水系沉积物中的Pt、Pd异常为研究对象，选择相容性接近的7对元素比值Cr/Ni、Nb/Ta、Pd/Pt、Rb/Cs、Sr/Ba、Th/U和Zr/Hf以及CaO、TFe2O3作为地球化学示踪指标，对龙场地区水系沉积物的物质来源组成进行了示踪探讨。结果表明：（1）龙场地区水系沉积物的物质来源主要为玄武岩风化产物，其中的高含量Pt、Pd是对玄武岩层中Pt、Pd高背景的继承和进一步浓缩富集；（2）根据对分布在灰岩区的水系沉积物物质来源的地球化学示踪研究，推测部分样品的物质来源应为玄武岩和灰岩风化产物；（3）根据对红岩村的水系沉积物物质来源的示踪研究，推断有热液活动和基性－超基性侵入体的物质成分，预测该地区具有一定的找矿远景。     

印度尼西亚苏门答腊岛低密度地球化学填图

为了快速获取印度尼西亚苏门答腊岛元素分布的详细情况,根据苏门答腊岛的地形及景观特征,以水系沉积物和土壤为采样介质,实施了覆盖全岛的1：100万低密度地球化学填图。详细介绍了1：100万低密度地球化学填图的野外工作方法、测试的元素及分析技术,根据测试结果制作了苏门答腊岛69种元素地球化学图,计算和分析了苏门答腊岛地球化学背景的特征参数。总结了苏门答腊岛不同成因类型组合元素的分布特征及规律,圈定了16处地球化学综合异常。结合主因子综合异常特征以及区内典型矿床(点)空间分布、规模,对苏门答腊岛主成矿元素综合异常进行了甲、乙、丙分类,包括6个甲级综合异常、4个乙级综合异常和6个丙级综合异常,并优选3处具有较好找矿潜力的甲级综合异常进行异常解释和讨论,认为HS7综合异常具有寻找SEDEX型铅锌矿的潜力,HS8和HS11综合异常具有寻找浅成低温热液型金银矿和矽卡岩型铜铅锌矿床的潜力,为苏门答腊岛深入开展矿产勘查提供参考和依据。     

Stream sediment geochemical exploration for gold in Central Eastern Desert,Egypt: Application of the concentration-number fractal model,factor analysis,and geochemical mineralization probability index

Geochemical exploration by stream sediment sampling using bulk leach extractable gold (BLEG) technique and applying concentration-number (C-N) fractal model, factor analysis (FA), and geochemical mineralization probability index (GMPI) resulted in the recognition of new Au occurrences around the Sukari gold mine in the central Eastern Desert of Egypt. The geochemical data of 128 stream sediment samples collected from the study area was used for delineating the geochemical anomalies and characterizing the dispersion trains of ore and associated elements (Au, Ag, As, Sb, Cu, Pb, Zn, Mo). Statistical analysis of the geochemical data applying the C-N fractal modeling enabled us to identify significant anomaly and background populations of the investigated elements and to construct reliable geochemical anomaly maps. Factor analysis using centered log-ratios (CLR), to address the problem of closed compositional data, revealed significant element associations for mineralization (Au, As, Mo, Zn, Ba), country rock compositions (Rb, Li, Be, Sn, Bi for granite, and Co, Cr, Ni for mafic rocks), and element mobility (e.g. Sb, Zr, and Ag). Weak and moderate Au anomalies that cannot be detected by factor score maps can be delineated clearly by using the C-N fractal method and GMPI distribution map. Our study revealed that Ag, As, and Sb are the main pathfinder elements for gold mineralization in arid to semiarid regions exemplified by the Sukari gold district. Silver can be used as a “direct” pathfinder, whereas As and Sb are “indirect” pathfinders for Au in such regions. The spatial distribution of Au and Ag anomalies indicate that gold mineralization in the Sukari district is structurally controlled. However, the spatial distribution of Cu, Pb, Zn, and Mo is controlled by mineralogical and lithological factors and is not related to any significant base metal deposits.     

Effects of pH fluctuations on potentially toxic metals in the water and sediment of the Dillon Reservoir,Summit County,Colorado

Potentially toxic metals exist in many reservoirs of surface water and therefore require an understanding of their occurrence, distribution, and mobility. The sediment accumulating at the bottom of the Dillon Reservoir, Colorado is contaminated with metals (Cu, Pb, Zn, Cd, Mo, etc.) that are primarily sorbed to Fe and Al hydroxides present in the sediment. The metals are derived from weathering of mineralized bedrock and mine tailings in the surrounding drainage basins. Sediment samples from the Dillon Reservoir were analyzed for major and trace elements and acidification experiments were performed to quantify the fraction of metals released from the sediment as a function of changes in pH. The highest percentages of metals are released from the sediment at low pH with the exception of Mo which has the highest percent released at near neutral pH. In addition, seasonal fluctuations in the concentrations of metals in the water of the Dillon Reservoir can be explained by changes in pH of as low as 0.2 pH units.     

Tectonic terranes, metallogeny and regional geochemical surveys: an example from northern British Columbia

This study utilizes three major data sources: distribution of geological units; density, type, age and distribution of mineral deposits; and elemental analyses from regional geochemical stream sediment surveys to define parameters that ‘characterize’ tectonic terranes in northern British Columbia. A similar approach could be applied anywhere in the Canadian Cordillera.This area, NTS map sheets 104N, 104O and 104P along the British Columbia-Yukon border, forms a transect through allochthonous terranes into North American rocks. These are: the allochthonous island-arc Stikine, oceanic Cache Creek, cataclastic Yukon/Tanana, and island-arc Quensel terranes, the pericratonic Dorsey terrane; the parautochthonous oceanic Sylvester allochthon; and the autochthonous miogeoclinal North American Cassiar terrane. Plutonic rocks of Jurassic-Cretaceous to Tertiary age intrude all terranes.Data sources used in the study are geological base maps and reports, the Ministry of Energy Mines and Petroleum Resources' mineral deposit database (MINFILE) and analytical data from the National Regional Geochemical Survey stream sediment and water sampling program.Geological maps were compiled from various sources and plotted to act as bases for geochemical and mineral deposit overlays for analysis and interpretation.Geochemical samples were separated into background and anomalous populations and compared according to their source terranes. We found that mean concentrations from background sample populations for some elements are statistically distinctive for different terranes. Unfortunately, elemental correlation coefficients for the terranes are similar so cannot be used to characterize each terrane.Data on mineral deposits and occurrences were compiled from minfile and other sources. Particular attention was paid to deposits with histories of production or significant reported reserves. Deposits were sorted by type and commodity to produce synoptic metallogenic maps.The combined data from geological, geochemical and mineral deposit databases form a strong tool for interpreting and predicting patterns of mineralization.     

基于元素含量和空间变异系数的化探异常信息识别

化探异常信息识别是化探数据分析最重要的任务之一, 也是化探数据在资源勘查领域受到广泛关注的最重要原因, 前人对化探异常信息识别做过大量研究, 这些研究中的大多数主要关注化探示踪元素的含量, 近而根据含量指标计算异常阈值, 而对示踪元素在空间中的分布特征关注较少。本文选择 1: 20万比例尺的克拉玛依幅为研究区, 根据区内金矿的矿床地球化学特征选择Ag、As、Au和Sb等4种元素为本区内金矿的示踪元素, 以地球化学元素分散晕形成理论为依据, 使用GIS技术和Matlab软件绘制研究区内4种金矿示踪元素的综合地球化学异常图。结果表明, 与传统阈值方法得到的化探异常图相比, 本文得到的化探异常图能够更好地指示研究区内已知金矿。     

Baseline geochemical mapping of Sardinia (Italy)

A total of about 20,000 stream sediment samples from about 13,000 km² were collected in Sardinia and analysed for eleven elements (Ag, Co, Cr, Cu, F, Hg, Mn, Mo, Ni, Pb, Sb and Zn) by Ente Minerario Sardo (EMS), aimed at mineral exploration. We have reutilized 16,890 samples (covering an area of 7987 km²) of the above data to compile geochemical baseline maps for all single elements as well as maps showing the regional variability of factor scores resulting from R-mode factor analysis. This type of maps has a particular relevance to environmental issues, especially in a region such as Sardinia which has been mined since pre-Roman times.