Statistical map analysis of regional stream-sediment data from Australia

In a regional stream-sediment survey of the Seigal and Hedleys Creek areas, covering approximately 6000 km², in all 2508 stream-sediment samples were collected with an overall sample density of 1 per 2–3 km². The minus 180 μm fraction of the samples was analyzed for up to 25 elements including As, Ba, Be, Bi, Ce, Co, Cr, Cu, F, Fe, Li, Mn, Mo, Nb, Ni, Pb, Rb, S, Sn, Th, Ti, U, W, Y and Zn.Selected elements were processed by a statistical map-analysis technique to: (a) display the broad-scale regional distribution patterns of the elements using a cell-average gap-fill mapping technique followed by low-pass filtering (LPF); and (b) delineate anomalous areas using the picture frame filter (PFF) and the Kolmogorov-Smirnov filter (KSF).The regional distribution patterns of elements clearly relate to geologic belts, plutons and stratigraphic units. Anomaly filtering clearly identifies the various known mineral occurrences including U, U-Cu-Sn, and Pb-Zn. The technique also delineated several anomalies, unrelated to known mineral occurrences, having similar anomalous element combinations and occurring in similar geological settings as those related to known mineral occurrences. Some of these filter-enhanced anomalies are too subtle to be immediately apparent in the unprocessed data.     

Geochemical patterns from local to global

The historical development of geochemical exploration is, in a sense, a process of progressive enlargement of areal coverage by exploration projects and progressive widening of sampling space. Along with this process, a hierarchy of geochemical patterns from small to large is gradually discovered and understood. In this paper, we try to summarize systematically the whole hierarchy of geochemical patterns from local, regional, provincial, megaprovincial to global, using examples obtained in China.Local anomalies (various types of dispersion halos, trains and fans) within areas not exceeding a few km², can be delineated when sampling is done with very close intervals in limited areas. Regional anomalies within areas of tens to hundreds km² and threshold values lower than local anomalies can be identified only when large areas of more than thousands of km² are mapped with wider space sampling. Geochemical provinces with areas of thousands or tens of thousands of km² can be discovered if even larger areas, of more than tens or hundreds of thousands of km², are covered with very low density sampling. More than millions of km² should be covered in order to discover geochemical megaprovinces somewhere in the world. Such megaprovinces are often associated with extraordinarily large mineral resources. If ultra-low density geochemical mapping can be carried out across national boundaries on a continental or global scale, we could find even broader geochemical patterns which will reflect the global tectonic features.The classification of geochemical patterns according to their sizes is necessary because it will be extremely useful in planning sampling layout in order to hit targets of certain size ranges. This in turn is arranged in different geochemical projects for achieving specific aims.     

Hydrogeochemical methods for base metal exploration in the northern Canadian shield

The use of lake waters for base metal exploration has been studied in the northern part of the Slave Geological Province of the Canadian Shield. The area is north of the treeline, within the zone of continuous permafrost, and, like most other regions of the Shield, has a high density of small lakes.A regional sampling of 1218 lakes established that less than 2 ppb (μg/l) Zn or Cu is typical of waters from unmineralized terrane. These samples had a median pH of 6.8 and a median specific conductivity of 19.5 μmhos. Lake waters were also taken from the areas surrounding five massive sulphide occurrences: High Lake, Canoe Lake, Takiyuak Lake, Hackett River and Agricola Lake. In all cases there are unambiguous anomalies for Zn. Anomalies are also present for Cu, but are less intense and extensive. This difference between the two elements is related to the superior mobility of Zn in surface waters and its more consistent presence as a major constituent of massive sulphides.A water sampling apparatus has been developed and tested on a light turbine helicopter. Using this, thirty sites may be sampled each hour when sampling at a density of 1 site per 2.8 km². Measurement of pH, conductivity and water temperature are recorded in the helicopter during sampling.A number of factors have been investigated that may influence the utility of lake water sampling for base metal exploration:

1. (1) Seasonal variability, while present to moderate degree, is unlikely to hinder application of the method.

2. (2) For the size of lakes sampled (2 km² or less), elements are homogeneously distributed across the lake surface during the ice-free season. During the initial period of break-up there are marked variations in element content around the ice-free lake margin. Sampling during this period may help define the source of metals for anomalous lakes.

3. (3) Study of sample preservation suggests that mobile elements, such as Zn, that are stable in solution within lakes, are also relatively stable when untreated water is stored in plastic bottles.

4. (4) Care must be taken to avoid contamination of the samples, particularly from the bottle.

The areal extent of lake water base metal anomalies appears to be less than equivalent lake sediment anomalies. Thus for wide-interval, regional geochemical reconnaissance, lake sediment sampling is the method of choice. Lake waters are an appropriate medium for detailed exploration of areas of interest, such as volcanic belts. For this application, the principal attractions are rapid sampling rates, and hence low costs, high contrast anomalies, and a uniform sampling medium.     

Regional reconnaissance exploration rock geochemistry for massive sulphides, New Brunswick, Canada

In the Bathurst District of New Brunswick there are more than 50 known occurrences of base metal sulphide mineralization within an area of Palaeozoic volcanic-sedimentary rocks approximately bounded by the Rocky Turn deposit in the north, the Key Anacon deposit in the east, the Heath Steele deposit in the south, and the Devil's Elbow deposit in the west. Only four of these occurrences are, or have been, producing mines; 19 are classed as “major occurrences”. The area is highly prospective for massive sulphide deposits of the Brunswick Mining and Smelting and Heath Steele type; it would obviously be of considerable importance to define the zones within the sequence where major occurrences should be sought.To determine whether exploration rock geochemistry could be used on a regional reconnaissance scale, 419 samples of rhyolite from an area of 2000 km² (at an average density of one sample per 5 km²) were analyzed for total content of Cu, Pb, Zn, Ca, Mg, K, Na, Fe, and Mn. The data were processed by calculating the geometric mean of all samples in cells of approximately 10 km². Contrary to the relations documented on a mine scale (within one kilometre of major deposits), where the clearest halos are given by major elements, it is the ore elements that give the best regional patterns.The producing mines and the most important of the known occurrences all lie in zones where rhyolite contains less than 10 ppm Cu. Element ratios considerably enhance anomalous relations. The Zn:Pb ratio of the sulphides in the main deposits is 2.4–2.8, regardless of grade. It is demonstrated that all present and past producing mines and the most important known major occurrences lie within well-defined zones of Zn:Pb ratios of 2.4–2.8. Similarly, zones where the Pb:Cu ratio is > 3.0 and the Zn:Cu ratio is > 7.0 also define the most important deposits. These ore-element relations derived from a low sample-density survey define priority zones for detailed exploration for significant major massive sulphide deposits.     

The use of “loam” concentrates in geochemical exploration in deeply weathered arid terrains

This paper reviews some aspects of the use of “loam” (soil) concentrates in geochemical surveys in arid, deeply weathered environments.An orientation survey at a small Ni-Cu-Co prospect in Western Australia has shown that discrimination between mineralized and unmineralized samples could be achieved using Ni, Cu, Co, Cr, Zn, As, Sn, Sc, Ti, Yb and Y in the coarse fraction of heavy concentrates. However, at the same prospect the best contrast for Ni, Cu and Co in surface samples was provided by analysis of the same fraction following a cold ammonium citrate/hydroxylamine hydrochloride digestion.At a nearby, larger prospect, some 54 km² in area, concentrates were separated, by jigging, from bulk soil samples, themselves composites of representative subsamples. Sampling at a density of 4 samples per km² revealed 1–2 km² size anomalies of Cu, Ni, Co, Cr, As and Au which could be related, variously, to known Ni-Cu and Au mineralization.In Botswana, analysis of concentrates, separated by tabling from samples collected at a density of 1 sample per 7.5 km² over an area of 5400 km², identified distinctive geochemical districts. Enhanced values of Au and of Cu-Ni in the concentrates were relatable to known mineralization and the results suggested that there were also Sn-W-Mo-Bi (granitoid) and Au-Pb-Zn-Bi-Sn (volcanogenic) associations which could lead to new prospecting targets. Anomalies of certain elements (for example, Cu in an ultramafic environment) may be more readily detected in surface material by “enrichment indexing” the concentrate data.     

National-Scale Geochemical Mapping Projects in China

Regional, national and global scale geochemical mapping projects have been carried out in China since the late 1970s, due to the development of cost‐effective, low detection limit analytical methods. These projects have provided a huge mass of high‐quality, informative and comparable data for mineral resource exploration and are now making contributions to environmental assessment. In this paper, four national‐scale geochemical mapping projects are described. (1) The Regional Geochemistry‐National Reconnaissance Project (RGNR project), which is China's largest national geochemical mapping project, has covered 6 million km² of upland regions since 1978. Generally, stream sediment samples were collected at a density of 1/km² and four samples were composited into one sample and analysed for thirty‐nine elements. (2) The deep‐penetrating geochemical mapping project (DEEPMAP Project) has been conducted since 1994 in covered terrains, including sedimentary basins, at a density of 1 sample per 100 km² with thirty to seventy elements determined per sample. In the past 10 years, an area of approximately 800 000 km² has been covered and this project has played an important role in finding sandstone‐type uranium deposits in basins. (3) The seventy‐six geochemical element mapping project (76 GEM project) has been carried out since 1999 and involved the collection of stream sediment samples from the RGNR project targets which were analysed for seventy‐six elements. Samples from each 1:50 000 map sheet were composited into one analytical sample (approximately one composite sample per 400 km²). Approximately 1 million km² have been surveyed to date. (4) The multi‐purpose eco‐geochemical mapping project has been conducted since 1999 in Quaternary plain areas for environmental and agricultural applications. Surface soils (depths from 0–20 cm) were collected at a density of one sample per km², and four samples were composited into one for analysis. Deep soils (from a depth of 150 to 200 cm) were collected at a density of one sample per 4 km² and four samples were composited into one analytical sample. All the composite samples were analysed for fifty‐four elements.     

Pathfinder applications of arsenic, antimony and bismuth in geochemical exploration

The potential applications of As, Sb and Bi as pathfinder elements in geochemical exploration have been researched using a new, rapid technique for the simultaneous determination of the three elements. Following a warm hydrochloric acid sample leach, the volatile hydrides of the elements are generated and flushed into an inductively-coupled plasma linked to an emission spectrometer. The technique offers a combination of good analytical precision and detection limits of 100 ppb for each of the elements.The principal sulphide ore minerals commonly contain traces of As, Sb and Bi, and concentrations of more than 1% of any one of these have been found in some sulphide specimens. During sub-aerial oxidation of sulphides, any As, Sb and Bi present is released and forms dispersion patterns in the surficial environment. Geochemical surveys of localities in the United Kingdom have demonstrated that anomalous dispersion trains of these elements can be detected in the sediments of streams draining the mineralized localities. In a geochemical mapping programme covering 16,000 km² of central Nepal, over 3500 stream sediment samples were analyzed for As, Sb and Bi, and many known occurrences of Cu, Pb and Zn mineralization are reflected by As, Sb and Bi anomalies. However, bedrock lithology appears to be an important factor influencing Sb and Bi dispersion patterns.In the areas studied, some or all of the elements As, Sb and Bi produce stream sediment anomalies that compare favourably in terms of contrast and extent with the heavy metal expressions, even though none of the three elements have been reported as important constituents of the mineralization with which they occur.     

Deep-penetrating geochemistry for sandstone-type uranium deposits in the Turpan–Hami basin, north-western China

The Turpan–Hami basin, covering an area of approximately 50,000 km² in NW China, contains concealed sandstone-type U deposits in a Jurassic sequence of sandstone, mudstone and coal beds. Sampling of soil profiles over the Shihongtan concealed U deposit in this basin shows that fine-grained soil collected from the clay-rich horizon contains U concentrations three times higher than similar soils at background areas. Selective leaching studies of these soils show that U is mainly associated with clay minerals, which comprise from 17.9% to 40% (average 30.4%) of the total mineral content. This may indicate that U is converted to uranyl ions [UO₂]²⁺ under oxidizing conditions and is sorbed on clay minerals to accumulate in anomalous concentrations. Fine-grained soil (<120 mesh, <0.125 mm) from the clay-rich horizon, generally occurring at a depth of 0–40 cm, is shown to be an effective sampling medium for deep-penetrating geochemical surveys. A wide-spaced geochemical survey at a density of approximately 1 site per 100 km² was carried out throughout the whole basin using this sampling medium. Samples were analyzed for 30 elements by ICP-MS following a 4-acid extraction. Three large-scale geochemical anomalies of U and Mo were delineated over the whole basin. One of the anomalies is consistent with the known U deposit at Shihongtan in the western part of the basin. A new potential target in the eastern part of the basin was selected for a follow-up survey at a density of 1 sample per 4 km². A drilling exploration programme at the center of the geochemical anomaly delineated by this follow-up survey discovered a new U deposit.     

Orientation studies for gold in the central pediplain of the Saudi Arabian shield

Orientation studies were carried out by the BRGM mission in Saudi Arabia between 1982–1986 to investigate the dispersion of gold in soils and wadi sediments and to define the optimum sample medium around eight prospects in the central Arabian pediplain. A comparison of gold distribution in several sieved fractions with various pedologic horizons shows that the distribution of gold changes abruptly from the coarser sizes near the source to the finest sizes 150 m downstream.The coarse fraction recommended by previous workers is not representative and yields erratic results in the specific environment of the pediplain. Gold is enriched and more homogeneously distributed in the minus 80 μm fraction of the skeletal soils and wadi sediments.Regional geochemical survey can be effective using a sensitive analytical method for gold and the minus 80 μm fraction of the brown gravelly sediment with a minimum density of 2 samples per km². Geochemical halos in the 30–50 ppb range indicate gold mineralization 500 to 1000 m upstream, depending on relief.In a first follow-up stage, continued use of the same size of the upper argillaceous layer with a regular reg sampling grid gives more contrasted and more extensive anomalies than using a coarse material. These anomalies may be slightly offset by the present arid erosion. A second follow-up stage is then recommended at a closer grid and sampling the brown blocky layer below the surficial reg pavement. Again, the use of the finest fraction at this exploration stage has given the best probability of finding a blind gold target.Optical determination of gold on a nonmagnetic fraction of heavy panconcentrate is not recommended, because nugget growth is practically absent in the present arid conditions and flour-sized gold particles are lost in desliming samples.     

1:50 000山东毕郭幅地球化学数据集

该数据集依托中国地质调查局“山东莱州-招远地区金矿整装勘查区矿产调查与找矿预测”项目,在充分收集地质、物探、化探、遥感及矿产等资料基础上,开展毕郭幅矿产地质调查。项目共采集1 875件水系沉积物样品,采样粒级为-10～+80目,平均采样密度4.5个/km²。采用电感耦合等离子质谱法（ICP-MS）、原子荧光光谱法（AFS）、粉末发射光谱法（ES）和石墨炉原子吸收光谱法（GF-AAS）分析了16种元素,最终形成1：50 000山东毕郭幅地球化学数据集,数据集包含有1 875件样品×16种元素的原始分析数据表格一个,图集一套（含有1张矿产地质图、一张采样点位图和16张元素地球化学图）。区内共新发现单元素地球化学异常149处,综合异常10处,结合地质、矿产、物探、化探、遥感等信息并圈出金矿找矿靶区5处。     

Cryptic sediment-hosted critical element mineralization from eastern Yunnan Province,southwestern China: Mineralogy,geochemistry, relationship to Emeishan alkaline magmatism and possible origin

A previous study briefly described the occurrence of a new type of Nb(Ta)-Zr(Hf)-REY-Ga (REY: rare earth elements and yttrium) polymetallic mineralization in eastern Yunnan, southwest China. In this paper, the mineralogical and geochemical features have been further advanced through a study of two regionally extensive and relatively flat-lying mineralized layers from No. XW drill core. The layers are clay-altered volcanic ash and tuffaceous clay, and are dominated by clay minerals (mixed layer illite/smectite, kaolinite, berthierine, and chamosite); with lesser amounts of quartz and variable amounts of anatase, siderite and calcite; along with trace pyrite, barite, zircon, ilmenite, galena, chalcopyrite, and REE-bearing minerals. The mineralized samples have higher Al₂O₃/TiO₂ values (13.7–41.4) and abundant rare metal elements (Nb, Ta, Zr, Hf, REE, Ga, Th, and U) whereas less mineralized samples are rich in V, Cr, Co, and Ni and have lower Al₂O₃/TiO₂ values (2.32–7.67). The mineralized samples also have strong negative δEu in chondrite-normalized REE patterns. Two processes are most likely responsible for the geochemical and mineralogical anomalies of the mineralized samples: airborne volcanic ash and multi-stage injection of low-temperature hydrothermal fluids. Based on paragenetic analysis, this polymetallic mineralization is derived from the interaction between alkaline volcanic ashes and subsequent percolation of low-temperature fluids. The intense and extensive alkaline volcanism of the early Late Permian inferred from this study possibly originated from the coeval Emeishan large igneous province (ELIP). This unique Nb(Ta)-Zr(Hf)-REE-Ga mineralization style has significant economic and geological potential for the study of mineralization of the lowest Xuanwei Formation.     

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.     

Regional geochemical reconnaissance of the Cordillera Occidental of Ecuador: economic and environmental applications

A regional geochemical reconnaissance survey of the Cordillera Occidental of Ecuador was initiated in 1995 as a sub-component of a wider Mining Development and Environmental Control Technical Assistance Project (PRODEMINCA) in Ecuador. The 36,000 km² survey area encompasses oceanic and continental-margin volcano-sedimentary terranes with known occurrences of porphyry-style Cu-Mo, exhalative massive sulphide, epithermal Au and mesothermal polymetallic mineralisation. A survey sample medium of <177 μm stream sediments was selected following an orientation study in the vicinity of known porphyry Cu mineralisation. In the 2–4°S sector of the Cordillera Occidental for which data are presented, 4850 drainage samples were collected at an average density of 1 per 2.57 km². All were analysed for 36 major and trace elements (Au, Ag, Cu, Pb, Zn, Mo, Ni, Co, Cd, Bi, As, Sb, Fe, Hg, Mn, Te, Ba, Cr, V, Sn, W, La, Al, Mg, Ca, Na, K, Sr, Y, Ga, Li, Nb, Sc, Ta, Ti, Zr). A stringent quality-control procedure included the systematic analysis of certified reference samples, field duplicates and replicates, data for which were used to calculate analytical precision, temporal drift and practical detection limits. Results for this part of the cordillera highlight the contrasting lithogeochemical signatures of the ocean-floor basalt terrane (Pallatanga Unit), the island-arc terrane of the Macuchi Unit, the continental volcanics of the Saraguro Group and the acid and intermediate lavas extruded from the Late Miocene to the Quaternary. Regional geochemical images for Au and associated pathfinder elements are dominated by anomalies relating to known mines and prospects. New exploration targets, often inconspicuous at the regional scale, have however been identified through the normalisation of data for individual lithological units against their respective geochemical backgrounds. In addition to mineral exploration, the drainage geochemical dataset for the Cordillera Occidental provides an unparalleled environmental baseline against which the impacts of future anthropogenic activities (including mining) may be assessed. A basis for the formulation of pragmatic sediment quality criteria and for the identification of natural geochemical hazards is also provided.     

Elemental Concentrations of Stream Sediments in Southern China

Over 3 million samples were collected from southern China at a density of 1–2 stream sediment samples per square kilometre as part of the Regional Geochemistry National Reconnaissance (RGNR) programme of China initiated in the late 1970s. Approximately 5244 composite samples of stream sediments from twelve provinces of southern China were prepared from the original RGNR samples collected from a territory with an area of 2300000 km² at a density of one composite sample per 1:50000 map sheet (about 400 km²). Seventy‐six elements were determined by the geoanalysis laboratory of Henan Province (platinum‐group elements) and by the Institute of Geophysical and Geochemical Exploration (IGGE) laboratory for the remainder. Internal quality and external quality control methods were applied to ensure that the analytical data were comparable. Statistics were used to derive the mean and background values and indicate the average concentrations of the seventy‐six elements. Comparisons were made against the mean values obtained from stream sediments, floodplain sediments, overall sediments and overall soils of the entire territory of China. The concentrations of Hg, Cd, rare earth elements and 24 other elements were higher than their background for the whole of China. In contrast, the concentration of Na₂O, CaO, Ba and Sr were lower in the stream sediments in southern China than their whole China background.     

Geochemical exploration in China

Geochemical exploration in China was commenced in the early 1950's. In 1951, the first experimental work was carried out in Yeshan, and a geochemical exploration section was set up in the Ministry of Geology in 1953.Regional geochemical reconnaissance (metallometric surveying) was initiated in 1956 on a nation-wide scale. Soil samples have been collected, and analyzed by semiquantitative spectrography. The results were heavily biased and were not adequately processed and utilized. Renewed efforts have been made to reprocess the vast amount of data accumulated and to utilize them more fully in mineral exploration.Meanwhile, another nation-wide project of regional geochemistry using more refined techniques is in its preparatory stage. It is the Regional Geochemistry-National Reconnaissance Project. In this project stream sediment sampling with a density of one per km² will be used in China Proper, and low-density sampling of various kinds of media in different environments will be used in remote areas. Pilot surveys covering areas of several thousand square kilometers are being undertaken in several provinces.Beside regional reconnaissance, geochemical prospecting has been carried out at virtually all phases of mineral prospecting in China.A brief summary of current research in exploration geochemistry taken by research institutes and universities is given, including studies on the methodology of regional geochemical surveys, primary halos around various types of ore deposits, mercury vapor survey techniques, refinement of analytical methods and instrumentation, and computerized data processing and plotting techniques.Several case histories are described where geochemical exploration techniques have led to successful ore discoveries in China.     

固体矿产地球化学勘查进展与成果

为庆祝第三十届国际地质大会在北京召开,让世界各国地质同行们了解中国地矿部门固体矿产地球化学勘查工作的进展,本文主要介绍我国地球化学勘查的成果。近十五年来已完成区域化探覆盖面积517万km2,中比例尺化探普查面积约90万km2,发现各类化探异常约4.3万处,通过检查化探异常和工程验证发现具工业价值的大、中、小型矿床569处,找矿效果非常显着,特别是化探找金、银矿方面取得突破性成果,化探方法技术不断提高和广泛推广。特殊景观区的野外工作方法、化探样品微量、痕量元素测试方法技术、化探异常的查证方法及化探数据处理与成图等方面均接近或达到国际水平。回顾过去,地球化学勘查进展迅速,成果丰硕,技术水平不断提高。展望未来,地球化学勘查目标明确,任务繁重,地质找矿潜力巨大。     

Geochemical exploration of a Precambrian Batholith, source of a Cu-W mineralization of the tourmaline breccia in Southern Finland

The Hämeenkyrö batholith is a round-shaped plutonic body of an areal size of 147 km². It is composed of calc-alkaline to alkaline rocks that intruded previously metamorphosed Svecofennian volcanogenic and sedimentary schists 1860 Ma ago. The Cu-W bearing tourmaline breccia of the Ylörvi deposit occurs in metavolcanic rocks close to the eastern contact of the batholith.The average sampling density in the batholith was 1 sample per km², and 175 samples were analyzed for Cu, Au, Ag, Ni, Pb, Co, Zn, S by AAS for SiO₂, TiO₂, Al₂O₃, FeO, MnO, MgO, CaO, Na₂O, K₂O, As, Sn and P by X-ray fluorescence. Mo and W were determined colorimetrically. Barth mesonorms were calculated for each sample and the rock type was determined according to Streckeisen's classification. Element distributions are displayed on contour maps.The rock types of the batholith exhibit an asymmetric concentric arrangement, the order from the center towards the margin being alkali-feldspar granite, syenogranite, monzogranite, quartz monzonite, quartz syenite, alkali-feldspar, quartz syenite, syenite and alkali-feldspar syenite. Anomalously high Cu, As, Sn, S, K₂O and Na₂O contents have been found at the eastern margin of the batholith in a N—S-trending zone, which is characterized by hydrothermal alteration phenomena, propylitization, tourmalinization and scapolitization. Three anomalous areas have been defined within this zone, one of them is associated with the Ylöjärvi deposit and the other two are regarded as exploration targets.     

Ground-water geochemistry of uranium and other elements, Monticello area, New York

About 500 well and spring waters were collected on an approximately 1-km spacing in an area centered on six small U and Cu-U occurrences near Monticello, N.Y., as an orientation survey in the NURE program. Rocks of the area belong to the Devonian Catskill Group and are predominantly red sandstones and shales of fluvial origin. The sediments dip 0–5° in the main part of the area, but steepen to 45° in the east. The ground waters were analyzed for 46 elements plus several other water properties.An R-mode factor analysis extracted 10 factors. The strongest factor, termed “Dissolved solids”, has heavy loadings on most major elements, plus U, B, Li, Sr, and Zn. This factor is attributed to varying degrees of interaction between original rainwater and rocks. Recognition of anomalies for elements loaded on this factor is aided by evaluation of ratios or plots against total dissolved solids or conductivity. Three weaker factors apparently represent admixtures with two types of deep brine and with waters of enhanced Fe-Mn resulting from reducing conditions. Other factors include an assemblage of insoluble trace metals and a Zn-Cu-P factor, both possibly related to contamination and/or analytical problems, a rare earth group, and an Se-As-Ag factor. The waters are clearly complex mixtures of effects.The geographic distribution of high U values shows some correlation with the distribution of U occurrences, but many equally high values occur outside the known mineralized area. When the data are projected to a vertical section normal to the strike, high U values define two gently dipping aquifers. The upper anomalous aquifer contains the known occurrences but extends downdip. Samples within this aquifer show patterns in U, dissolved O₂, and conductivity, apparently related to influx of fresh water from updip, along major rivers, and along possible fractured zones. High He values are also most numerous near the occurrences and define the deeper U-rich aquifer. The interpretation of the data is greatly clarified by separation of individual aquifers.Saturation indices are generally −3.4 to −5 and show patterns similar to dissolved U, except for values of −6 to −9 in a few samples with high phosphate. Predominant U species are usually UO₂(CO₃)₂²⁻, or less commonly UO₂CO₃⁰ or UO₂(HPO₄)₂²⁻.