共查询到20条相似文献，搜索用时 31 毫秒
1.
Major and trace elemental compositions of loess samples collected from the Jingyuan section in the northwestern Chinese Loess Plateau (CLP) were analyzed to investigate the potential impacts of grain size sorting and chemical weathering on the loess geochemistry and to extract appropriate geochemical indices for better evaluating the East Asian monsoon variability. Based on variations of major and trace elements in different grain size fractions, seventeen elements were classified into three types: (1) Si and Na display higher contents with the increased particle sizes; (2) Al, Fe, Mg, K, Mn, Zn, Rb, Cr, V are mainly enriched in fine size fractions; (3) Ti, Ba, Zr, P, Ca and Sr show irregular variations among different size fractions. Comparison of Al-normalized elemental ratios with Zr/Rb and Rb/Sr ratios (two commonly employed indicators for grain size sorting and pedogenic weathering) indicates that Si/Al, Zr/Al, Ti/Al variations match well with Zr/Rb and grain size results, whilst Ca/Al, Sr/Al, P/Al ratios display similar variability as that of Rb/Sr ratio. Comparison of loess based proxies (e.g., elemental ratios, magnetic susceptibility, grain size) of Jingyuan section with speleothem and ice-core records confirms that elemental ratios of high-resolution loess sequences developed in the northwestern CLP can be employed to address fluctuations of the winter monsoon-induced grain size sorting and summer monsoon-related weathering and pedogenesis at glacial–interglacial and millennial timescales. 相似文献
2.
沉积物的元素地球化学特征是对沉积盆地水体环境以及古气候条件变化的响应。本文根据元素（Al、Fe、Mg、Ca、K、Na、P、V、Ni、Co、Cr、Cu、Zn、Sr、Ba、Cd、Li、Mn、Pb、Ti）的含量及其比值（Al/Ti、Fe/Mn、Sr/Ba、Mg/Ca、Sr/Ca、Na/Ca、V/Cr、Ni/Co、Ni/V）的变化，对三水盆地古近系心组红岗段生油层的沉积条件进行了系统分析。心组红岗段下部（亚段A）表现为较稳定的地球化学特征。各元素丰度及其比值指示这一时期陆源输入持续较高、且物源组成变化不大。由于海水入侵的影响，湖盆水体盐度相对较高，底部水体以弱氧化条件为主，O2-H2S界面位于水/沉积物界面附近。红岗段中上部（亚段B、C）的元素地球化学特征变化较为频繁且幅度很大，反映古气候和湖盆沉积条件的迅速变迁。在潮湿气候条件下，沉积物的地球化学特征表现为以Al、Ti为代表的外源元素含量及其比值较高，而Mg、Ca等盆内化学沉积元素含量较低。古氧气指标指示底部水体为还原环境，有利于有机质保存。因而，相应于较高的有机碳含量。在间歇性干旱时期，陆源输入减少，外源元素含量及其比值显著降低。随着蒸发作用的加强，水体盐度加大，内源元素丰度以及Mg/Ca、Sr/Ba、Sr/Ca和Na/Ca比值大幅度上升。底部水体为氧化环境，O2-H2S界面多位于水/沉积物界面或沉积物中。上述两种气候条件在红岗段中上部沉积时期交替出现。红岗段沉积后期由于淡水的长期输入，湖水出现逐渐淡化趋势。 相似文献
3.
Based on 225 analyses of quartzites, siliceous granoblastites,calc silicate rocks, calcite and dolomite marbles, including120 analyses of pelites and semipelites, sedimentary trendsof chemical variation are identified in staurolite and sillimanitegrade rocks. The correlation of original clay mineral contentwith Ti, Fe, K, Rb, Y, Nb, Ca, Ni, Ga, Zn and probably Ba andMn is shown. A similar clay mineral (whose composition is calculated)was added to all the sediments except the quartz-rich sandstones,now quartzites. This pattern appears to be general for mostsediments, based on crustal averages. The form of the originaladdition of Sr in the sediments might be identified as eithercarbonate or feldspar by a Ca vs. Sr plot. The southern pelites in a 2–4 km peripheral zone to theConnemara orthogneisses and migmatites have been metasomatized.The crude order of elemental enrichment from the elements increasedthe most to those increased the least relative to the same stratigraphicalhorizons in the north is: Mn, Ba, Th, Cu, Ca, Sr, Y, Pb, Zn,Pr, Ge, Nd, La, Mg, S, Ce, Rb, Sm, Ti, Na, K and Ga while Si,Al, Cr, Ni, Co, Fe and P are unchanged or removed. The sourceof the material added is postulated to be the water-rich residualfraction of the migmatitic quartz diorite gneiss, the transportbeing by movement of a water-rich fluid out of the migmatites,the fixation being mainly in biotite and new, more calcic, plagioclaseporphyroblasts, there being a positive correlation between elementenrichment and ionic radius. 相似文献
4.
Four overbank profiles from the three terraces of different age were sampled in 10 to 20 cm intervals for the bulk content of major and minor (Ca, Mg, Fe, Ti, Al, Na, K and P) and trace (Mo, Cu, Pb, Zn, Ni, Co, Mn, As, U, Th, Sr, Cd, Sb, V, La, Cr, Ba, W, Zr, Ce, Sn, Y, Nb, Ta, Sc, Li, Rb and Hf) elements in the minus 0.125 mm fraction. Univariate statistics together with analysis of variance discriminated between the lower-lying carbonate (CA) population dominantly composed of carbonates and the overlying silicate (SI) population being dominantly of silicate mineralogy. This stratified pattern resulted from the intensive erosive action of melting glaciers exerted on limestones and dolomites in the alpine region, followed by local inputs mainly of silicate composition. Elements exhibiting the greatest between-population variability are Ca and Mg being enriched in the CA population and Fe, Mn, P, Sr, Al, Na, K, Li, Rb, Y, Zr, Ni, Cr and Ti being enriched in the SI population. Anomalously high Hg, Pb and Ba concentrations (maximum values: 6,500±2,860 ppb, 225±13 ppm and 1,519±91 ppm, respectively) in the lowermost part of the profile S7, which is nearest to the Croatian-Slovenian border, derive from the mineralized Slovenian catchment area. This profile also contains trimodal frequency distributions of Fe, Mn and P whose highest concentrations coincide with increased values of Zn and Cu which are bimodally distributed. Geochemical patterns of majority of elements in all four profiles consistently reflect the average compositions of the upstream drainage basins. 相似文献
5.
山东招远前孙家金矿床地质和元素地球化学研究 总被引：6，自引：1，他引：5
对矿区地表和井下四个中段共采集地层、岩体、蚀变岩、石英脉和矿体样品503件,测试了Au、Ag、As、Sb、Cu、Pb、Zn、Sn、Bi、Mo、Co、Ni、Mn、Cr、V、Ti、Ba、Rb和Sr等19种元素的含量,运用Suffer软件编制了19种元素的矿脉地球化学纵剖面图,根据格里戈良分带指数法计算了元素的地球化学分带,建立了原生晕地球化学立体分带模式。综合地质地球化学资料分析得出以下认识：由花岗岩→钾长石化花岗岩→绢英岩化花岗岩→绢英岩→石英脉或硅化带→金矿石,随着蚀变作用增强,成矿元素Au、Ag、As、Cu、Pb、Bi、Mo、Sb增加,然而成矿作用主要发生在绢英岩化后的硅化阶段。矿区成矿元素Au、Ag、As、Cu、Pb、Sn、Bi、Mo、Co．Ni含量呈多峰分布,分布范围大,离散度大,其中Au、Ag高含量峰值区峰型突出,成矿富集趋势强烈。矿区成矿阶段可分为：石英-金-黄铁矿阶段、石英-金-多金属硫化物阶段和石英-碳酸盐阶段。F1因子（Au、Ag、As、Co、Ni、Sn、Bi）为主成矿阶段的元素组合,F3因子（Mo、Sb）和F5因子（Cu、Zn）反映了成矿热液活动的多期叠加。F4因子Rb、Sr、Ba组合在本区最具典型意义,Rb与Sr、Ba为对抗性元素,Sr、Ba、Ca低值带,Rb、K高值带恰好与Au、矩高值带吻合,显示花岗岩长石类矿物的钾长石化和绢云母化与成矿关系密切。与矿体的侧伏方向一致,总体上矿脉纵剖面地球化学高值带均向SW侧伏。其中Au、Ag高值带宽且比较连续,上下均未封闭,结合金矿体虽已出露地表但规模不大和原生晕分带特征,推测为一浅剥蚀矿床,向SW深部仍有一定延深。矿区原生晕分带序列自上而下为（Hg2、Sr、Ba、Rb）→（矩、Au、Sn、Mo、Cu→（Zn、Pb）→（Sb、Mn）→（Ni、V、Co、As、Hg1、Bi）。As、Sb、Hg高值带偏于中下部,可能指示下部隐伏矿体的存在。 相似文献
6.
太平洋北部铁锰结核富集区沉积物的元素地球化学特征 总被引：2，自引：1，他引：2
本文对太平洋北部铁锰结核富集区沉积物的元素地球化学作了较为详细的研究。因子分析提供的信息表明,元素的分布主要受三个因子控制:（1）粘土及Fe、Mn氧化物水化物胶体的吸附作用;（2）生物化学作用过程有关的自生沉积作用;（3）海底页岩风化及附近海区的火山喷发作用。元素的来源:（1）Fe、Mn、Cu、Co、Ni、Zn、Cr、Cr、Mg、Al、Ti、K共生,主要来自粘土吸附;（2）C有机、N、Sr、Na及Si、Ca、Sr主要来自生物化学过程沉积;（3）Pb主要来源于岩石碎屑（火山喷发碎屑）。 相似文献
7.
Granulometric and chemical composition of the Sava River sediments upstream and downstream of the Krsko nuclear power plant 总被引：2，自引：2，他引：0
Total concentrations of 13 elements (K, Ca, Ti, Cr, Mn, Fe, Cu, Zn, Rb, Sr, Y, Zr, Pb) in the size-fractionated Sava River sediments upstream and downstream of the Krsko nuclear power plant together with metal speciation within bulk sediment have been investigated. Trace metals generally increase with decreasing particle size, however, because of entrapment of organic matter in the 0.63–1 mm fraction, concentrations in the coarser sediment fraction are higher than expected. Exchangeable Pb, Zn, Cu, Mn, Cr and Fe are generally found to represent a negligible fraction of the total metal concentration of the bulk sediment. Seasonal variations of the Pb, Zn and Cu concentrations in the <0.5 mm fraction reflect decreased values during the spring period. Heavy metal concentrations in the 2003 waste water discharges from the Krsko nuclear power plant released into the Sava River were much lower than their maximum allowed values. Combined rubidium and organic matter normalization of the Zn, Pb and Cu concentrations, which was applied on the minus 0.063 mm fraction, indicated three potential sources of contaminants. 相似文献
8.
First experiences with a tube-excited energy-dispersive X-ray fluorescence in field laboratories 总被引：1，自引：0，他引：1
U. Kramar 《Journal of Geochemical Exploration》1984,21(1-3)
An energy-dispersive X-ray fluorescence system, equipped with air-cooled X-ray tube, Si(Li)-detector, a 20-sample changer, and a minicomputer was adapted to a mobile laboratory, installed in a Landrover 109. With this system different conditions for the excitation of characteristic lines of trace elements were tested and compared with the qualities of a previously used radionuclide-excited system. Up to 18 elements can be determined simultaneously in the course of one measurement (K, Ca, Ti, Mn, Fe, Ni, Cu, Zn, Ga, As, Rb, Sr, Y, Zr, Nb, W, Pb, and Th). For most elements concentrations in common rocks are clearly above the detection limits (e.g., Ni to Pb, 5 ppm; Th, 10 ppm).Two case histories (Kaiserstuhl, F.R.G. and Bastnäs, Central Sweden) demonstrate the applicability of the mobile tube XRF. 相似文献
9.
A new method of simultaneous multi-elemental analysis, Proton Induced X-ray Emission (PIXE), was used to detect trace elements in waters associated with a coal strip-mining operation in southern Indiana. Stream, pond, and ground water samples were collected and analyzed monthly from, or near, Sulphur Creek in Sullivan County. The concentrations of 26 major and trace elements were determined in samples from eleven locations: K, Ca, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, As, Se, Br, Rb, Sr, Mo, Cd, Sn, Sb, I, Ba, Hg, Pb, and U. Elemental concentrations fluctuated considerably throughout the 13-month sampling period and also among sampling sites. Nickel, Zn, As, Cd, Mn, Fe, and Ca were highest in the upstream water which was most acidic (pH = 2.9–4.0) because of old unreclaimed mining operations. The highest values recorded were Ni = 1662 ppb, Zn = 4953 ppb, As = 26 ppb, Cd = 93 ppb, Mn = 5063 ppb, Fe = 63 ppm, and Ca = 325 ppm. The concentrations of these elements decreased downstream as the pH of Sulphur Creek increased which was likely due to the influence of the calcareous glacial till cover in the area and the recent mining activity which disturbed overburden containing a high percentage of calcareous materials. Lead, I, Br, and Ti values were highest (661 ppb, 86 ppb, 70 ppb, and 45 ppb, respectively) in the ground water from the coal seam (pH approximately 7). Other elements which were relatively high in the pH 7 waters closest to the current mining operations (pond, stream, and groundwater) included K (17 ppm), Sr (3408 ppb), Ba (173 ppb), As (14 ppb), Rb (16 ppb), Sn (14 ppb), and Cu (3840 ppb). The highest Cu concentration was recorded at the point where drainage water from the mine entered Sulphur Creek. Gallium, U, Hg, and Mo were found in low (< 13 ppb for Ga and Hg; < 205 ppb for Mo and U) concentrations and only in the ponds within the mine. 相似文献
10.
位于特提斯成矿域西段塞尔维亚Bor成矿带内的Mali Krivelj铜矿床是一大型斑岩型矿床。为揭示该矿床热液蚀变作用过程及元素迁移规律,文章对新鲜安山岩及不同蚀变带典型样品进行了微量元素分析及元素迁移质量平衡计算。研究结果表明,绢英岩化带及绿泥石-绢云母化带显示类似元素迁移规律,REE、Sr、Ba、Zr、Th、U、Ti、Co、Ni等元素显示一定程度迁出,而Rb、Cs等元素显示一定程度迁入,绿泥石-绢云母化带发育大量磁铁矿,而绢英岩化带则大量出现石英+绢云母+黄铁矿组合,这表明随着流体的持续演化,流体的还原性逐渐增强。青磐岩化带蚀变较弱,其元素迁移程度较低。研究区Cu与Cr、Rb、Ti/Sr、Rb/Ba、Cr/Zn比值等具较好的正相关性,Cu与REE、Ba、Zn、Mn、Sr等元素具有一定的负相关性,表明该矿床全岩元素迁移规律在一定程度上也能作为地球化学勘查指标为寻找斑岩矿化中心提供依据。 相似文献
11.
Significant differences are noticed in major and trace element compositions between the Yangtze River and the Yellow River surface sediments.The former sediments are rich in some major elements such as K,Fe,Mg,Al,and most of the trace elements which show wide variations in element concentrations,whereas the Yellow River sediments only have higher Ca,Na,Sr,Ba,Th,Ga,Zr,Hf contents and show slight variations in element contents.In the Yangtze River Basin are widely distributed intermediate-acid igneous rocks and complicated source rocks together with strong chemical weathering which determine the elemental compositions of the Yangtze River sediments,while the elemental compositions of the Yellow River sediments are decided by the chemical composition of loess from the Loess Plateau and intense physical weatering.Cu,Zn,Sc,Ti,Fe,V,Ni,Cr,Co,Li and Be can be used to distinguish the Yangtze River sediments from te Yellow River sediments and be treated as tracers for both the sediments to study the processes of their mixing and diffusion in the coastal zones of China. 相似文献
12.
用X-荧光光谱测定岩石中低量稀土元素的仪器参数和测定条件,文[1]已作过讨论。本文介绍样品分析所采用的基本校正,谱线重叠校正和背景处理方法,并将这些方法应用于其他少量和痕量元素的测定。基体的吸收校正岩石样品中最重的主元素是铁,镧系元素La～Er的La线和Ti,Sc,Cr,Mn,Fe, 相似文献
13.
Sujatha Dantu 《Environmental Earth Sciences》2014,72(4):955-981
Regional-scale variations in soil geochemistry were investigated with special reference to differences among soil groups and lithology in an area of 9,699 km2 in Medak district, Andhra Pradesh, India. The concentrations of 29 elements (major: Si, Al, Fe, Mn, Mg, Ca, Na, K, Ti, P and trace: As, Ba, Cd, Co, Cr, Cu, F, Mo, Ni, Pb, Rb, Se, Sr, Th, U, V, Y, Zn, Zr) in 878 soil samples collected (557-topsoil, 321-subsoil) at a sampling density of 1 site/17 km2 from 557 sites representative of all the soil types present in studied area were determined, and their elemental composition are discussed. The baseline levels of these elements in soils are determined over different lithological units for the identification of anomalous values relative to these. For the first time, geochemical maps for Medak district are prepared on 1:50,000 scale and the lithogeochemical database generated provides information on the lateral and vertical distribution of elements in soil. The spatial variations in the distribution of elements reflect underlying geologic characteristics. Box-plots reveal that the concentration of most of the elements in soils were not strongly dependent on the soil group but the soil-geochemistry abruptly changes with the change in the soil parent materials indicating that the distribution of elements is mostly influenced by the bedrock lithology and other natural processes acting on them. For instance, the concentrations of Co, Cu, Fe, Mn, Ti, V and Zn are high in soils developed on basaltic terrain while the soils developed on granitic and gneissic terrain exhibit high elemental concentrations of K, Pb, Rb, Si, Th and Y. Alfisols had relatively high contents of elements while entisols had lower concentrations of most of the elements. The database can be used in the chemical characterisation of different geological units as well as applications in various environmental and agricultural fields. The results indicate that regional geology is an important determinant of soil geochemical baselines for soil pollution assessment and further emphasizes the importance of determining background levels locally. The defined baselines can be used to establish background values for future soil surveys. 相似文献
14.
Sixty-five samples of rocks, soils, plants and well waters in the Mamandur area have been analysed for Cu, Zn, Pb, Sr, K, Na, and Mn by atomic absorption spectrophotometry. Among the plants, Waltheria indica Sterculiaceae is confined to mineralised ground in the area. This plant is characterised by maximum concentration of Zn, Cu, Mn, Rb, Sr, Na and K, and is to that extent, a valuable (though not an infallible) indicator of base-metal mineralisation. It is shown that there is considerable difference in the intake of elements by plants in relation to the concentration of the same elements in the soils and well waters of the area. 相似文献
15.
Factors affecting the distribution of potentially toxic elements in surface soils around an industrialized area of northwestern Greece 总被引：2，自引：0，他引：2
Alexandra Petrotou Konstantinos Skordas Georgios Papastergios Anestis Filippidis 《Environmental Earth Sciences》2012,65(3):823-833
In order to investigate the factors influencing the distribution of 32 potentially toxic elements in the Ptolemais–Kozani
basin, northwestern Greece, 38 soil samples were collected and analyzed. Concentrations of Al, Ca, Fe, K, Mg, Mn, Na, P, Ti,
Ba, Co, Cr, Cu, La, Li, Ni, Pb, Sc, Sr, V, Y, and Zn were determined by ICP-AES and concentrations of As, Bi, Cd, Cs, Mo,
Rb, Sb, Th, Tl, and U by ICP-MS. Bivariate analysis, principal component analysis, and geostatistical analysis were employed
to investigate the factors influencing the distribution of the elements determined in the study area. The results indicate
that the distribution of the majority of elements determined, especially for Cr, Ni, and associated elements, is greatly influenced
by the geology and geomorphology of the study area. Principal component analysis has yielded four factors that explain over
77% of the total variance in the data. These factors are as follows: lithophilic elements that are associated with Al silicates
minerals of K (factor I: 29.4%), ultramafic rocks (factor II: 20.5%), elements that are coprecipitated with Fe and Mn oxides
(factor III: 18.0%), and anthropogenic activities (factor IV: 9.3%). The anthropogenic activities that influence the distribution
of several potentially toxic elements (i.e., Cd, Cu, Pb, Zn) are agricultural practices and the deposition of fly ash in the
vicinity of the local power stations. 相似文献
16.
The primary halos of porphyry copper deposits are characterized by compositional zoning in three dimensions. Two ideal zoning patterns can be divided in accordance with the shape of primary halos in space: bell-shaped and anticline-shaped. In the process of alteration-mineralization, K, Si, (OH), Fe, Cu, Mo, Ag, S, Ba, Rb, Pb, Zn, As, etc. were imported, while Na, Ca, Mg, Fe, Al, Ti, Mn, V, Co, Sr, Pb, Zn, etc. were exported or became activated, and then transported and reprecipitated. Both import and export of Fe, Pb and Zn may have taken place. The fundamental factors controlling the zoning of primary halos are: the stability of complexes and the activity of elements; pH, Eh, the behaviour of sulfur and the sulphophile character of elements; the concentration of components and the regularities of isomorphism; temperature and pressure; and tectonic setting and lithological characters of wallrocks. The authors consider that the zoning patterns of primary halos in porphyry copper deposits are the outcome of integrated effects of various factors. 相似文献
17.
Bo Peng Adam Piestrzynski Jadwiga Pieczonka Meilian Xiao Yaozhu Wang Shurong Xie Xiaoyan Tang Changxun Yu Zhi Song 《Environmental Geology》2007,52(7):1277-1296
The mineralogy and geochemistry of the waste rocks distributed at Taojiang Mn-ore deposit, central Hunan province, China,
were studied using X-ray powder diffraction (XRD), electron microprobe analysis (EMPA) fitted with energy dispersive spectrometer
(EDS) and inductively coupled plasma mass spectrum (atomic emission spectra) ICP-MS (AES), with the aim of predicting the
environmental impacts of weathering of the waste rocks. The mineralogical results from microscope observation and XRD and
EMPA studies show that the waste rock is composed of black shale and minor Mn carbonates. The oxidation of sulfide minerals
such as galena, pyrite and chalcopyrite is accompanied by decomposition of Mn carbonates and K-feldspar during exposure to
atmospheric O2. The geochemical characteristics of major, rare earth elements (REE) and trace elements of the waste rocks also show that
the waste rock can be divided into black shale and Mn carbonate, and both of them are currently under chemical weathering.
The major alkalies and alkaline elements (Ca, Mg, Na, K, Rb, Sr and Cs) and major elements (Fe, S and P) and heavy metals
(Sc, V, Cr, Th, U, Sn, Co, Ni, Cu, Zn, Pb, Mo, Cd, Sb, an Tl) are being released during weathering. The mobility of alkalis
and alkaline elements Ca, Mg, Na, K, Rb, Sr and Cs is controlled by decomposition of Mn carbonates. The dispersion of Cr,
Sc and Th (U) might be related to weathering of K-feldspar, and the release of the heavy metals Co, Ni, Cu, Zn, Pb, Mo, Cd
Sb and Tl is dominated by the breaking of sulfide minerals. The REE of the waste rocks and surrounding soils and the spidery
distribution patterns of heavy metals in the waste rocks, the surrounding soils and the surface waters show that weathering
of the waste rocks and bedrock might be the sources of heavy metal contamination for the surrounding soils and surface water
system for the mining area. This is predicted by the mass-balance calculation by using Zr as an immobile element. Therefore,
it is urgently necessary take measures to treat the waste rocks distributed throughout the area for the local environmental
protection. 相似文献
18.
Eighteen Chinese geologic reference samples (stream sediments GSD 9–12, soils GSS 1–8, and rocks GSR 1–6) were analyzed by wavelength-dispersive X-ray fluorescence spectrometry (XRFS) for major elements Si, Ti, Al, Fe, Mn, Mg, Ca, Na, K, and P, and by energy-dispersive XRFS for trace elements Ba, Ce, Cr, Cu, La, Nb, Ni, Rb, Sr, Y, Zn, and Zr. Major element analysis followed gravimetric determination of loss on ignition, and samples were prepared by fusion with Li2 B4 O7 . A loose-powder sample preparation was used for trace element analysis. The results reported in this study are, generally, in good agreement with concentrations compiled by X. Xie of the Geochemical Standard Reference Group and the Institute of Geophysical and Geochemical Exploration (People's Republic of China). 相似文献
19.
Helmut Grohmann 《Mineralogy and Petrology》1965,10(1-4):436-474
Zusammenfassung Es wurden 122 Proben granitoider Gesteine, die größtenteils aus dem Bereiche der Alpen und der südlichen Böhmischen Masse stammen, mit Hilfe instrumenteller Methoden auf die Elemente Be, Ca, Co, Cr, Cu, Fe, Ga, K, Li, Ni, Pb, Rb, Sc, Sn, Sr, Ti, Tl, V, Y, Zn und Zr analysiert. Dabei fanden die Emissionsspektral-analyse und die Röntgenfluoreszenzanalyse Anwendung. Für die Bestimmung sehr geringer Konzentrationen der Elemente Pb, Sn, Tl und Zn in sauren Silikatgesteinen wurde eine spezielle Doppelbogenmethode ausgearbeitet.Aus den Analysendaten wurden die Durchschnittsgehalte der einzelnen Elemente errechnet und mit Literaturwerten über die Gehalte von seltenen Elementen in Granitoiden verglichen. Bei den meisten Daten wurde Übereinstimmung gefunden, bei einigen anderen (Be, Co, Ni, Rb, Sc) Korrekturvorschläge gemacht.Die Variationsbreiten der Konzentrationen der einzelnen Elemente wurden an Hand von Histogrammen beschrieben und kurz diskutiert.
Mit 4 Textabbildungen
Herrn Professor Dr.F. Machatschki zum 70. Geburtstag gewidmet. 相似文献
Summary 122 samples of granitoidic rocks from the Alps and the southern part of the Bohemian Massif were analysed for the elements Be, Ca, Co, Cr, Cu, Fe, Ga, K, Li, Ni, Pb, Rb, Sc, Sn, Sr, Ti, Tl, V, Y, Zn, and Zr by means of emission-spectrochemical analysis and X-ray fluorescence analysis. A special method employing a double arc was developped for determining very small concentrations of the elements Pb, Sn, Tl, and Zn in acid silicate rocks.The average contents of the individual elements were calculated from the data of analysis and compared with the data on the contents of rare elements in granitoidic rocks, as quoted in literature. In most cases the data were conformable, however, in some other cases (Be, Co, Ni, Rb, Sc) corrections were suggested.The ranges of the concentrations of the individual elements were described by means of histograms and were discussed briefly.
Mit 4 Textabbildungen
Herrn Professor Dr.F. Machatschki zum 70. Geburtstag gewidmet. 相似文献
20.
新疆霍什布拉克铅锌矿床地质、地球化学特征研究 总被引：3，自引：3，他引：3
新疆霍什布拉克铅锌矿床的矿体和含矿地层的产状一致,主矿体的矿石具有条带状、纹层状构造,矿石中大量发育霉球状、管状和环带状生物结构,显示出层控、热水沉积成因的特点。含矿地层和矿石样品的主量元素PER图解显示含矿碳酸盐岩以含石膏的灰岩为主,围岩的白云岩化微弱,矿化与硅化关系密切。矿石、含矿碳酸盐岩和页岩、粉砂质灰岩和泥质粉砂岩等碎屑岩具有各自鲜明的微量元素分布特征,上层矿体矿石中较强的富集过渡族元素Ti、V、Cr、Mn、Co、Ni、非活动性元素Zr、Hf及大离子亲石元素Sr和Pb,亏损活动性元素Na、K、Rb、Ba和非活动性元素Nb、Th。其围岩重结晶泥晶灰岩富集Ti、Mn、Ni、Sr和Pb,亏损Na、K、V、Fe、Rb、Ba、Zr、Hf、Nb和Th。下层矿体的围岩页岩和泥质、粉砂质灰岩样品的微量元素分布在平均上地壳线附近,部分样品较明显的富集Ti、V、Cr、Mn、Co、Ni、Rb、Y、Zr和Hf,亏损Na、Fe、Sr、Nb。上层矿体矿石和下层矿体围岩中的部分碎屑岩富集强亲岩浆元素Cr、Co、Ni,且上层矿体矿石的稀土元素分布模式具有强的正Eu异常,部分下层矿体围岩具有较明显的正Eu异常。地质和地球化学特征显示该矿床属于热水沉积矿床中的SEDEX型矿床。 相似文献