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1.
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. 相似文献
2.
3.
Overbank and medium-order stream sediment samples were collected in Belgium and Luxembourg from 66 sampling locations (area of about 33,000 km2) and analysed for major and trace elements among which Zn, Pb, Cu and As. At each sampling location large bulk samples were taken, namely in the lower (normally at ≥1.5 m depth, over an interval of about 20–40 cm) and upper (normally upper 5–25 cm) parts of the overbank profiles and from the stream sediments. Furthermore, at a number of these sites, a detailed geochemical analysis of vertical overbank sediment profiles (sampling intervals of 10–20 cm) was subsequently carried out to unravel element variations through time and to help in the overall evaluation. For most sampled sections evidences such as 14C-dating and the absence of anthropogenic particles point towards a pre-industrial and often pristine origin of the lower overbank sediment samples. From the latter bulk samples, mean background concentrations were deduced. They reveal the existence of significant differences between the northern and southern part of Belgium (incl. Luxembourg) which relate to the difference in geological substrate. In the north dominantly non-lithified Quaternary and Tertiary sands, marls and clays occur while in the south Palaeozoic sandstones, shales and carbonate rocks outcrop. Consequently separate mean background values were calculated for the two areas. In the southern study area, some anomalous metal concentrations have been recorded in pre-industrial sediments. They are derived from mineralised Palaeozoic rocks, a feature which could be of interest for base metal exploration. In the upper overbank and stream sediments, in general, higher heavy metal and As contents were recorded with highest values in areas with metal mining, metal melting and cokes treatment industries. By comparing the trace element concentrations of the upper overbank or stream sediment samples with the concentrations detected in the lower overbank samples at each of the sampling locations, and by evaluating the vertical distribution patterns where available, the degree of pollution of the alluvial plain and the present-day stream sediments can be assessed. From this exercise, it is clear that highest pollution occurs in the northern part of Belgium, which relates to its high population density and industrial development. 相似文献
4.
Mercury was determined in thirty‐three international stream sediment and soil reference samples (eleven Chinese soils, GSS‐1 to GSS‐11; twelve Chinese stream sediments, GSD‐1A to GSD‐12; four Canadian stream sediments STSD‐1 to STSD‐4; South African stream sediments, SARM‐42, SARM‐46 and SARM‐47; Japanese stream sediments, JSd‐1 to JSd‐3) by direct mercury analyser. Samples were taken in 500 μl quartz boats, placed in an auto sampler and processed (drying time 60 s at 300 °C; decomposition time 120 s at 850 °C; waiting time 45 s). The instrument was calibrated in the low (0‐50 ng) and high ranges (50‐500 ng) with two reference materials GSS‐5 and GXR‐2 (USGS). Using the calibration line, reference samples were analysed for Hg. The results of the determinations agreed with the recommended values of RMs in all cases except JSd‐1. The RSD calculated for the RMs was found to be within 20%. The detection limit was 1 ng g?1. 相似文献
5.
The suitability of floodplain sediment as a global sampling medium: evidence from China 总被引：2，自引：0，他引：2
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. 相似文献
6.
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. 相似文献
7.
R. Swennen J. van der Sluys R. Hindel A. Brusselmans 《Journal of Geochemical Exploration》1998,62(1-3)
A geochemical survey of Belgium and Luxembourg was carried out as part of an international research project entitled ‘Regional geochemical mapping of Western Europe towards the year 2000'. The aim of this research was to map regional background geochemical patterns based on pristine or at least pre-industrial overbank samples and to deduce regional information on the degree of environmental pollution of floodplain and present-day river sediments. Over the entire study area (about 33,000 km2), 66 overbank sites have been sampled. Catchment areas range between 60 and 600 km2. At each site an overbank profile has been dug out in the immediate vicinity of the river and described in detail. A first composite sample was taken 5–25 cm below the surface. This sample is supposed to represent deposition over the last centuries. Human interferences in this interval are often inferable based on changed sedimentary characteristics and the presence of anthropogenic particles such as charcoal, slags and brick fragments. A second composite sample was taken at depth, usually >1.5 m below the surface over an interval of about 20 cm. In most sites, the profile characteristics allowed to assume pre-industrial or even pristine conditions for this lower overbank sample. In some profiles this was confirmed by 14C-dating and/or by the absence of anthropogenic particles. Finally, a present-day stream sediment was sampled on the site to infer the actual pollution status. After drying at 80°C, disaggregation and sieving, the <125 μm fractions of the three sediment samples were analysed by XRF for major elements and several trace elements. Lower overbank samples generally show a direct link with the geological substrate and allow to assess natural background concentrations. Results from the mapping exercise as well as from the statistical analyses display a clear contrast between the northern part of Belgium where Cenozoic unconsolidated sandy and silty formations dominate which are especially vulnerable for erosion, and the southern part of Belgium and Luxembourg where Paleozoic and Mesozoic sandstones, carbonates, marls and shales are the prevalent lithologies. Here the shales are the most intensively eroded lithologies. This is especially reflected in the element patterns of Al2O3, MgO, K2O, Ga, Ni, Rb, Sc and V which negatively correlate with SiO2. Despite the human related pollution, the geological contrast between north and south Belgium is still recognisable in the geochemical pattern of the upper overbank and present-day stream sediment samples for the above-mentioned elements. Furthermore there is a clear increase in heavy metal contents (Zn, Cd, Pb, Cu), As and in certain locations in Ba from the lower to the upper overbank sediment, as well as to the present-day stream sediment. The relative increase in element content allows to assess the degree of pollution and helps to define those drainage areas where more detailed research is needed. 相似文献
8.
《Applied Geochemistry》2003,18(2):283-309
International agreements (e.g. OSPAR) on the release of hazardous substances into the marine environment and environmental assessments of shelf seas require that concentrations and bioavailability of metals from anthropogenic sources can be distinguished from those originating as a result of natural geological processes. The development of a methodology for distinguishing between anthropogenic and natural sources of metals entering the Irish Sea through river inputs is described. The geochemistry of stream, river and estuarine sediments has been used to identify background geochemical signatures, related to geology, and modifications to these signatures by anthropogenic activities. The British Geological Survey (BGS) geochemical database, based on stream sediments from 1 to 2 km2 catchments, was used to derive the background signatures. Where mining activity was present, the impact on the signature was estimated by comparison with the geochemistry of sediments from a geologically similar, but mining free, area. River sediment samples taken upstream and downstream of major towns were used respectively to test the validity of using stream sediments to estimate the chemistry of the major river sediment and to provide an indication of the anthropogenic impact related to urban and industrial development. The geochemistry of estuarine sediments from surface samples and cores was then compared with river and offshore sediment chemistry to assess the importance of riverine inputs to the Irish Sea. Studies were undertaken in the Solway, Ribble, Wyre and Mersey estuaries. The results verify that catchment averages of stream sediments and major river samples have comparable chemistry where anthropogenic influences are small. Major urban and industrial (including mining) development causes easily recognised departures from the natural multi-element geochemical signature in river sediment samples downstream of the development and enhanced metal levels are observed in sediments from estuaries with industrial catchments. Stream sediment chemistry coupled with limited river and estuarine sampling provides a cost-effective means of identifying anthropogenic metal inputs to the marine environment. Investigations of field and laboratory protocols to characterise biological impact (bioaccumulation) of metals in sediments of the Irish Sea and its estuaries show that useful assessments can be made by a combination of surveys with bioindicator species such as clams Scrobicularia plana, selective sediment measurements that mimic the ‘biologically available’ fractions, and laboratory (mesocosm) studies. 相似文献
9.
Kamil Vrana Stanislav Rapant Dušan Bodiš Karol Marsina Blanka Maňkovská Ján ?urlík Peter Šef?ík Jozef Daniel Ladislav Lu?ivjanský Jaroslav Lexa Silvester Pramuka 《Journal of Geochemical Exploration》1997,60(1):7-37
The Geochemical Atlas of Slovak Republic (49,036 km2) at a scale of 1 : 1,000,000 was compiled during 1991–1995 together with maps of associated geochemical and ecological features at a scale of 1 :200,000. Investigations were aimed at the evaluation of concentrations and distributions of Al, As, Ba, Be, Ca, Ce, Co, Cd, Cs, Cr, Cu, Fe, Ga, Hg, K, La, Li, Mg, Mn, Mo, Na, Ni, P, Pb, Rb, Sb, Se, Sn, Sr, Th, U, V, W, Y, Zn, Zr in groundwater (16,359 samples), stream sediments (24,422 samples), rocks (3839 samples), soils (9892 samples from 4946 profiles; A and C horizons of each profile were sampled) and forest biomass (the foliage of the forest tree species from 3063 plots was sampled). In groundwater field measurements of temperature, pH, conductivity, dissolved O2, acidity, alkalinity were done. The evaluation was oriented to the natural radioactivity of the Slovak territory as follows: rocks (K, U, Th, Utot and dose rate, 15,573 reference spectrometric points), radon risk and water (Unat, 226Ra, 222Rn; 5271 samples). The main objective of the Geochemical Atlas was to construct single-component maps showing concentrations of chemical elements, compounds and measured parameters in the researched media of Slovakia at a scale of 1 : 1,000.000 and to create interactive databases of chemical composition and/or measured parameters of groundwater, biomass, rocks, soils, stream sediments and natural radioactivity, for the entire territory of the Slovak Republic. The single-component maps are not constructed in the part ‘Rocks’, where all the main rocks types of Slovakia are presented in the ‘Map of lithogeochemical rock types of Slovakia at a scale of 1: 500,000’. The edition of six atlases has been planned. In 1997 the first three atlases will appear (Groundwater, Biomass, Natural Radioactivity). Publishing of last three atlases (Rocks, Soils, Stream Sediments) is planned for 1998. Since the analytical works on stream sediments were finished during 1997, it was not possible to present here the results of that part of the Geochemical Atlas. 相似文献
10.
High‐Precision Iron Isotope Analysis of Geological Reference Materials by High‐Resolution MC‐ICP‐MS 
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下载免费PDF全文 Yongsheng He Shan Ke Fang‐Zhen Teng Tiantian Wang Hongjie Wu Yinhuai Lu Shuguang Li 《Geostandards and Geoanalytical Research》2015,39(3):341-356
We report high‐precision iron isotopic data for twenty‐two commercially available geological reference materials, including silicates, carbonatite, shale, carbonate and clay. Accuracy was checked by analyses of synthetic solutions with known Fe isotopic compositions but different matrices ranging from felsic to ultramafic igneous rocks, high Ca and low Fe limestone, to samples enriched in transition group elements (e.g., Cu, Co and Ni). Analyses over a 2‐year period of these synthetic samples and pure Fe solutions that were processed through the whole chemistry procedure yielded an average δ56Fe value of ?0.001 ± 0.025‰ (2s, n = 74), identical to the expected true value of 0. This demonstrates a long‐term reproducibility and accuracy of < 0.03‰ for determination of 56Fe/54Fe ratios. Reproducibility and accuracy were further confirmed by replicate measurements of the twenty‐two RMs, which yielded results that perfectly match the mean values of published data within quoted uncertainties. New recommended values and associated uncertainties are presented for interlaboratory calibration in the future. 相似文献
11.
《Applied Geochemistry》2001,16(11-12):1323-1331
This paper reports the first results of a low-density geochemical survey covering the whole continental area of Portugal, taking both topsoils and active stream sediments as the sampling media. The data were obtained in a consistent way from 653 sites at a sampling density of 1 site/135 km2. The samples were analysed for 31 elements by ICP-AES and after quality control the following 19 were selected: Al, As, Ba, Ca, Co, Cr, Cu, Fe, K, La, Mg, Mn, Ni, P, Pb, Sr, Th, V and Zn. The baseline levels for these elements are presented. The first geochemical maps of Portugal were prepared and the geochemical patterns are generally well correlated to geological factors sometimes combined with anthropogenic influences. Some general trends can be observed between geochemical patterns and soils distribution. 相似文献
12.
Comparison of stream sediment and soil sampling for regional exploration in the eastern Alps,Austria
《Journal of Geochemical Exploration》1988,31(1):75-85
Tests in three different areas of the Austrian Alps showed that in mountainous areas, soil samples taken at the break of slope are an alternative sampling medium to stream sediments for regional geochemical exploration even if taken at the unusually low density of 1 sample/km2. B-horizon soil samples from the nearest break of slope were collected in conjunction with stream sediment orientation studies. The minus 0.2 mm fraction of all samples was routinely analyzed for the total contents of 36 elements. The results for the indicator elements in the three test areas (Area 1: Cu; Area 2: Ag, As, Cu, Pb, Sb, Sn, Zn; Area 3: As, Cu) showed that break-of-slope soil samples more clearly indicate known mineralization than drainage geochemistry. In the soils, almost all elements showed a higher natural variability of the data with considerably higher metal contents. In mountaineous regions, each soil sample will have a clearly defined area of influence. The break of slope represents a site where clastically and hydromorphically dispersed elements are concentrated. It is concluded that soil samples can be used for regional exploration using low sampling densities in mountaineous areas. At the same time they will provide valuable information for other fields of science (e.g. agriculture, forestry, environmental sciences) and are thus superior to stream sediments. 相似文献
13.
Zhizhong Cheng Hongku Huang Mei Liu Tiexin Gu Weidong Yan Mingcai Yan 《Geostandards and Geoanalytical Research》2013,37(1):95-101
The preparation and characterisation of four chromium ore reference materials are described in this paper. The sample material for GCr‐1, GCr‐3 and GCr‐4 was collected from chromite deposits in Tibet, Qinghai province and Inner Mongolia. GCr‐2 is a composite sample from GCr‐1 and GCr‐4. Sample homogeneity was tested by WD‐XRF and the relative standard deviations were < 1.0%. An F‐test showed that all four materials were homogeneous. Thirteen laboratories involved in the inter‐laboratory programme provided 672 determinations (eighteen oxides and elements). Sixteen components were characterised as certified values, of which Cr2O3 ranged from 17.59 to 57.80% m/m. The contents of FeO and CO2 were taken as reference values. 相似文献
14.
《Applied Geochemistry》2006,21(3):492-514
Geochemical mapping of northern Honshu in the Northeast Japan Arc was carried out using stream sediments at a sampling density of one sample per 130 km2. More than 50 elements were determined in 395 stream sediment samples (<0.18 mm fraction). In geochemical maps, areas with especially low concentrations of large ion lithophile elements (LILE), Be and Li widely overlap with the distribution of Quaternary volcanic rocks along the volcanic front. The areas rich in mafic elements are associated with mafic rocks in many cases. On a regional scale, Ni, Cr and Cu contents are higher in the eastern Paleozoic–Mesozoic basement zone, Pb and Tl tend to be higher on the western zones, and Zn and Cd are high in the western back-arc zone. The areas especially rich in Cu, Zn, Cd, Pb, Bi and Tl coincide with the distribution of large mineral deposits. High concentrations related to Kuroko, hydrothermal-vein, and skarn-type deposits are recognized. High values of As and Sb are related to active geothermal areas near volcanoes and ore deposits. Chemical variations of K, Ce, Th and Sn in the stream sediments are concordant with chemical variations in major rocks. The median and mean concentrations for the stream sediments in northern Honshu, showing arc signatures, are lower in Rb, Cs, Th, Li, K, Be, Ta, LREE, Ni, Hg and Sn, and higher in Sc, Ca and Cd relative to the whole area of Japan, largely because of the contribution of Cenozoic island-arc volcanic rocks that are generally poor in incompatible elements. The averaged chemical compositions of the stream sediments for the geologic zones show systematic variations of many elements. The contrasting variations of LREE and Th contents, which are lower in the zones of Cenozoic rocks relative to the zones of pre-Neogene basements, reflect the regional variations in the main rocks, and also reflect the change of geological settings of the studied area from the continental margin to an island arc during the Cenozoic. 相似文献
15.
Compared with solution ICP‐MS, LA‐ICP‐MS studies have thus far reported comparatively few external reference data for accuracy estimates of experiments. This is largely the result of a paucity of available reference materials of natural composition. Here, we report an evaluation of natural glass (obsidian) as an inexpensive and widely available external reference material. The homogeneity of over forty elements in six different obsidian samples was assessed by LA‐ICP‐MS. Accuracy was tested with two obsidian samples that were fully characterised by electron probe microanalysis and solution ICP‐MS. Laser ablation experiments were performed with a variety of ablation parameters (fluence, spot sizes, ablation repetition rates) and calibration approaches (natural vs. synthetic reference materials, and different internal standard elements) to determine the best practice for obsidian analysis. Furthermore, the samples were analysed using two different laser wavelengths (193 nm and 213 nm) to compare the effect of potential ablation‐related phenomena (e.g., fractionation). Our data indicate that ablation with fluences larger than 6 J cm?2 and repetition rates of 5 or 10 Hz resulted in the most accurate results. Furthermore, synthetic NIST SRM 611 and 612 glasses worked better as reference materials compared with lower SiO2 content reference materials (e.g., BHVO‐2G or GOR128‐G). The very similar SiO2 content of the NIST SRM glasses and obsidian (i.e., matrix and compositional match) seems to be the first‐order control on the ablation behaviour and, hence, the accuracy of the data. The use of different internal standard elements for the quantification of the obsidian data showed that Si and Na yielded accurate results for most elements. Nevertheless, for the analysis of samples with high SiO2 concentrations, it is recommended to use Si as the internal standard because it can be more precisely determined by electron probe microanalysis. At the scale of typical LA analyses, the six obsidian samples proved to be surprisingly homogenous. Analyses with a spot size of 80 μm resulted in relative standard deviations (% RSD) better than 8% for all but the most depleted elements (e.g., Sc, V, Ni, Cr, Cu, Cd) in these evolved glasses. The combined characteristics render obsidian a suitable, inexpensive and widely available, external quality‐control material in LA‐ICP‐MS analysis for many applications. Moreover, obsidian glass is suited for tuning purposes, and well‐characterised obsidian could even be used as a matrix‐matched reference material for a considerable number of elements in studies of samples with high SiO2 contents. 相似文献
16.
Hélène Balcone‐Boissard Agnès Michel Benoît Villemant 《Geostandards and Geoanalytical Research》2009,33(4):477-485
Concentrations of halogens (fluorine, chlorine, bromine and iodine) were determined in six geochemical reference materials (BHVO‐2, GS‐N, JG‐1, JR‐1, JB‐1b, JB‐2). Halogens were first extracted from powdered samples using a pyrohydrolysis technique, then hydrolysis solutions were analysed by ion chromatography for F and Cl and inductively coupled plasma‐mass spectrometry for Br and I. The detection limits in solutions were 100 μg l?1 for both F and Cl and 10 ng l?1 for Br and I. Considering the extraction procedure, performed on a maximum of 500 mg of sample and producing 100 ml of pyrohydrolysis solution, detection limits in rock samples were 20 mg kg?1 for F and Cl and 2 μg kg?1 for Br and I. The mean analytical errors on the studied composition ranges were estimated at 10 mg kg?1 for F and Cl, 100 μg kg?1 for Br and 25 μg kg?1 for I. The concentration values, based on repeated (generally > 10) sample analysis, were in good agreement generally with published values and narrowed the mean dispersion around mean values. Large dispersions are discussed in terms of samples heterogeneity and contaminations during sample preparation. Basaltic RMs were found to be more suitable for studies of halogen compositions than differentiated rock material, especially granites – the powders of which were heterogeneous in halogens at the 500 mg level. 相似文献
17.
Geochemical mapping of Shikoku in the SW Japan Arc was conducted using stream sediments (<0.18 mm fraction) with sample densities of 1 site per 106 km2. Concentrations of 51 elements in 173 stream sediments were determined. Areas with especially high Cr, Ni, Mg and Co concentrations run intermittently and linearly through Shikoku, and coincide with exposures of the Mikabu greenstone complex composed of oceanic basaltic and gabbroic rocks with minor ultramafic bodies. Areas with higher concentrations of Fe, V, Sc, Ti, Mn, Cr, Ni, Mg, Co and Eu are distributed widely along the Shikoku Island axis; they mainly overlap with the zones of the high-pressure type metamorphic rocks (Sanbagawa Belt) and of the Jurassic accretionary complexes with sedimentary rocks (Chichibu Belt): in contrast, areas with lower concentrations spread over the northern coastal zone of Cretaceous granitoids (Ryoke Belt) and in the southern coastal zone of Cretaceous-Paleogene accretionary complexes (Shimanto Belt). Distribution patterns of these elements reflect that various amounts of mafic and ultramafic materials, possibly of oceanic origin, are associated with the rocks in the Sanbagawa and Chichibu Belts, although such components occur sparsely in the Shimanto and Ryoke Belts. Calcium, Sr, Na, Nb, Sm and Gd contents are lower along the southern coastal zone. High values of Th, U, La, Ce and Ba are associated with granitic rocks. The positive anomalies of Cu and Cd coincide with the distribution of stratabound Cu deposits in the Sanbagawa Belt. Positive anomalies of Sb in the northern area are associated with Sb deposits near the large Median Tectonic Line fault zone. A high-Hg zone is present in the southern fore-arc area. The median concentrations for stream sediments in Shikoku are higher in Hg, Cu, Ni, Cr, Rb, Li, Cs, K, slightly higher in Nb, Ta, La, Ce, Sn and lower in Ca than those for average Japanese stream sediments. The median concentrations for the four geologic zones show systematic wide variations of mafic associated elements, and narrow variations of lithophile elements generally more abundant in felsic rocks. The chemical compositions of the stream sediments in Shikoku largely reflect the concentrations in the pre-Neogene accretionary complexes and in the high-P metamorphic rocks mainly formed from clastic materials derived from continental margins, and ratios of mafic and ultramafic materials within surface rocks; they are partly influenced by sulfide mineralization and fluid migration. 相似文献
18.
文章以浙江省平湖市为典型三角洲平原区,开展了多种尺度、不同采样方法的对比试验。结果表明,田块内土壤元素分布较为均匀,小范围内元素的空间分异性较小,而田块之间土壤元素含量差异性明显增加;Hg,Cd等典型污染元素空间分异性较强,而人为污染扰动较弱的元素的空间分布较为均一;不同采样方法取得的区域性资料,其统计值接近,空间分布模式也相似,但有些元素仍有较明显差异。因此,中大比例尺地球化学调查时,应根据调查研究的目标任务,充分考虑地块分布、土壤类型和土地利用方式,选择合理的采样点。土壤样品可采取多坑点采集、多子样组合的方式,以保证样品的代表性,同时减少分析测试工作量。 相似文献
19.
Ali Pourmand François L. H. Tissot Monica Arienzo Arash Sharifi 《Geostandards and Geoanalytical Research》2014,38(2):129-148
We present an open‐source algorithm in Mathematica application (Wolfram Research) with a transparent data reduction and Monte Carlo simulation of systematic and random uncertainties for U‐Th geochronometry by multi‐collector ICP‐MS. Uranium and thorium were quantitatively separated from matrix elements through a single U/TEVA extraction chromatography step. A rigorous calibrator‐sample bracketing routine was adopted using CRM‐112A and IRMM‐035 standard solutions, doped with an IRMM‐3636a 233U/236U ‘double‐spike’ to account for instrumental mass bias and deviations of measured isotope ratios from certified values. The mean of 234U/238U and 230Th/232Th in the standard solutions varied within 0.42 and 0.25‰ (permil) of certified ratios, respectively, and were consistent with literature values within uncertainties. Based on multiple dissolutions with lithium metaborate flux fusion, U and Th concentrations in USGS BCR‐2 CRM were updated to 1739 ± 2 and 5987 ± 50 ng g?1 (95% CI), respectively. The measurement reproducibility of our analytical technique was evaluated by analysing six aliquots of an in‐house reference material, prepared by homogenising a piece of speleothem (CC3A) from Cathedral Cave, Utah, which returned a mean age of 21483 ± 63 years (95% CI, 2.9‰). Replicate analysis of ten samples from CC3A was consistent with ages previously measured at the University of Minnesota by single‐collector ICP‐MS within uncertainties. 相似文献
20.
1:20万区域化探方法核心技术"取样粒级"的讨论 总被引：2，自引：0，他引：2
内蒙古区域化探扫面采用水系沉积物测量(或土壤测量),取粗粒级样品,取得了较好的地质找矿效果,但局部景观区找矿效果受到了一些影响.我国南北方水系沉积物中元素含量呈"U"形分布,反映了南北方不同的风化类型,以及所取不同粒级样品的物质成分也不同;取粗粒级和细粒级样品均可能有化探异常显示,采用-5～+20目(0.9 mm≤A＜4 mm)和-120目(A＜-0.125 mm)组合粒级作为采样粒级.为提高工效,取样时可以采用-5目(或-20目)全粒级物质,也能获取更多的找矿信息.这种取样粒级技术,也适宜于全国各种不同的景观区的不同尺度的水系沉积物测量和土壤测量的化探工作. 相似文献