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1.
Heterogeneous layers of granulite facies metamorphic basites of the Proterozoic supracrustal Faurefjell Formation in Rogaland, S.W. Norway, display an extreme chemical variation. Within a single layer the bulk chemical composition gradually changes from approximately basaltic in basic granulites to alumina-iron-rich in granofelses. Component-ratios and composition-volume relations indicate open-system chemical reactions mainly involving the extraction of silica. Apparent enrichment in Fe, Ti, P, Al, Zr, Ni, Co, Zn, Y, Nb, Hf and REE and variations in resulting metamorphic mineral assemblages are related to premetamorphic progressive lateritisation of a basaltic protolith. The weathering generated a continuous chemical suite from SiO2=48 wt%, Fe2O3=10 wt% and Al2O3=19 wt% in the basic granulites to 14 wt%, 40 wt% and 25 wt% in the Fe-Al granofelses. Metasomatism during diagenesis and during (very) high-grade metamorphism (1200–900 Ma) further perturbed the concentrations of relatively mobile elements Ca, Mg, K, Rb, Sr, Ba, Na and Li in the laterites without affecting the transition metal ratios. In particular, the REE did not fractionate differentially during the supracrustal and metasomatic alteration.  相似文献   

2.
大黑山铝土矿赋存于上二叠统宣威组底部,下伏地层为峨眉山玄武岩。矿石结构主要以泥晶结构为主,具有少量鲕状、粒屑结构。矿石构造以致密块状构造为主,局部呈层状、似层状。铝土矿石中Al2O3与Fe2O3、Si O2呈现较好的负相关关系,Ti O2与Zr、Hf、Nb、Ta相关性较好,Zr-Hf、Nb-Ta的相关性拟合度很高。铝土矿与峨眉山玄武岩样品具有相似的稀土元素配分模式。综合稳定元素相关性、微量元素及稀土元素标准化图解、lg Ni和lg Cr二元图解等分析方法对大黑山铝土矿的成矿物质来源进行探讨,研究结果表明铝土矿的成矿物质来源主要来自峨眉山玄武岩。  相似文献   

3.
This paper reports a geochemical study on the major and trace elements and Pb–Sr isotopes of a weathering profile developed in the Lower Cambrian black shales in central Hunan (China). Six weathering horizons were identified and sampled vertically throughout the profile. The chemical composition of the profile consists of variable concentrations of the major elements Fe2O3, FeO, MnO, MgO, CaO, Na2O, and P2O5 and of less variable concentrations of SiO2, TiO2, Al2O3, and K2O. The chemical change caused by weathering is estimated by mass-balance calculations, and the results show that the element mobility is characterised by substantial loss of SiO2, FeO, CaO, K2O, Na2O, LOI, Cr, V, Ba, Cs, Rb, Sr, U, and Th, and moderate loss of Al2O3, MgO, Fe2O3, Ni, Cu, Pb, Tl, Sn, Sc, Ge and REE (Y). The high field strength elements TiO2, Sn, Sc, U, Ga, Ge, Zr, Hf, Nb, and Ta were immobile during weathering. The chemical changes and the Pb–Sr isotopic data suggest that four types of chemical reactions occurred: the oxidation of sulphide minerals (e.g., pyrite) and organic carbon (OS), the dissolution of less resistant clinochlore-Ia, calcite, and P-bearing minerals (DL), the dissolution of detrital albite and microcline (DA), and the transformation of clay (TC) minerals (e.g., muscovite and illite–smectite). These chemical reactions then led to two stages of geochemical processes, an early stage of chemical differentiation and a later stage of chemical homogenisation. The chemical differentiation dominated by the OS, DL, and DA reactions, led to the leaching of mobile elements (e.g., MgO, Na2O, K2O, P2O5, Sr, and REE) and the redistribution of some less mobile elements (e.g., SiO2 and Al2O3). In contrast, the chemical homogenisation, which was caused by TC reactions, led to the leaching of both mobile and less mobile elements from the system and ultimately transformed the weathered black shales into soil. Soils derived from black shales in South China might result from the above two geochemical processes.  相似文献   

4.
The Minim-Martap plateau bauxite deposit, located between the Minim and the Martap villages, is one of the 11 plateaus within the Minim-Martap bauxite region. The plateau has an elevation of 1294 m above sea level, with three to more 30 m thickness of bauxite horizon. These plateaus were formed as result of supergene weathering of volcanic rocks occurring as dissected flow basalt landscapes that form relatively flat plateau rising steeply from the surrounding granites. The bauxite deposit of the plateau is lateritic, with the surface of the plateau been completely covered by indurated caps. Seventeen bauxite samples were collected from the plateau and prepared for geochemical analysis. Whole rock analysis was carried out using the X-ray Fluorescence technique and ICP-MS was used for trace elements investigation. Statistical analysis reveals that average values of Al2O3 (54.87%), Fe2O3 (7.17%), SiO2 (2.44%), and TiO2 (4.54%) indicate the plateau bauxite deposit is an of a world class standard with very little impurities compared to the standard major element contents of bauxite (>?40% A12O3, less than <?20% Fe2O3, and less than <?8% combined SiO2). Abundant trace elements include Zr, Ce, Sr, V, Ba, La, Nd, Ga, and Nb. Weathering due to chemical alteration indices using the Ruxton ratio and CIA approaches revealed the plateau have undergone intense weathering process that formed the bauxite deposit. Three different classification systems indicate it as a low iron-rich bauxite deposit. Precursor rock investigation indicates the origin of the bauxite is mafic, basaltic andesite igneous rocks with intermediate pH (basic–acidic characteristic).  相似文献   

5.
This present study describes the geochemistry of fluvial sediments of the Palar river (lower reaches), Southern Peninsular India, with an aim to evaluate their provenance, weathering and tectonic setting. The bulk sediment chemistry is influenced by grain size. The river sediments are enriched with SiO2 and depleted in Al2O3, K2O, CaO, Na2O, MgO, P2O5, MnO, Fe2O3 as compared with UCC values. Geochemical classification indicate that the sediments are mainly arkose, wacke and shale in composition. Discriminant diagrams together with immobile element ratio plots reveal that, the Palar river sediments are mostly derived from rocks formed in an active continental margin. Additionally, the rare earth element ratios as well as chondrite-normalized REE patterns with flat HREE, LREE enrichment, and negative Eu anomalies indicate felsic rock sources. The chemical indices of alteration suggest that Palar river sediments are chemically immature and have experienced low chemical weathering effects. This is further supported by the Th/U Rb/Sr ratio and A-CN-K ternary diagram, with most of the sample data points falling close to the plagioclase-smectite line. The bivariate plot of Th/Sc versus Zr/Sc suggest a moderate recycled origin of the sediments.  相似文献   

6.
This present study describes the elemental geochemistry of fluvial sediments in the Kurigram (upstream) to Sirajganj–Tangail (downstream) section of the Brahmaputra–Jamuna River, Bangladesh, with the aim of evaluating their provenance, weathering and tectonic setting. Petrographically, the sediments are rich in quartz (68%), followed by feldspars (8.5%) and lithic grains (7%). The bulk sediment chemistry is influenced by grain size. Concentrations of TiO2, Fe2O3, MgO, K2O, P2O5, Rb, Nb, Cr, V, Y, and, Ce, Th and Ga slightly decrease with increasing SiO2/Al2O3 and grain size, suggesting clay matrix control. In contrast, concentrations of CaO, Na2O, Sr and Pb increase with increasing SiO2/Al2O3 and grain size, suggesting residence of these substances in feldspar. Decrease in Zr as grain size increases is likely controlled both by clay matrix and heavy minerals. In addition, heavy minerals' sorting also influences Ce, Th, Y and Cr abundances in some samples. The sediments are predominantly quartzose in composition with abundant low-grade metamorphic and sedimentary lithics, low feldspars and trace volcanic detritus, indicating a quartzose recycled orogen province as a source of the sediments. Discriminant diagrams together with immobile element ratio plots show that, the Brahmaputra–Jamuna River sediments are mostly derived from rocks formed in an active continental margin. Moreover, the rare earth element ratios as well as chondrite-normalized REE patterns with flat HREE, LREE enrichment, and negative Eu anomalies indicate derivation of the sediments of Brahmaputra–Jamuna River from felsic rock sources of upper continental crust (UCC). The chemical indices of alteration suggest that Brahmaputra–Jamuna River sediments are chemically immature and experienced low chemical weathering effects. In the A–CN–K ternary diagram, most of the samples close to the plagioclase–K-feldspar join line and to the UCC plot, and in the field of various lithologies of Higher Himalayan Crystalline Series, suggesting that rocks in these series are likely source rocks. Therefore, the elemental geochemistry of the Brahmaputra–Jamuna River sediments is controlled mostly by mechanical breakdown of lithic fragments and subsequent preferential attrition of muscovite > albite > quartz.  相似文献   

7.
《Geodinamica Acta》2013,26(5):343-362
The Mendejin area, NW Iran, is part of the western Alborz-Azarbaijan zone which is one of the most structurally—and magmatically-active zones of Iran. Volcanic rocks with calc-alkaline and, locally, alkaline features cover an extensive part of this zone. The Mendejin volcanic rocks, Eocene-Oligocene in age, include tuffs and volcanoclastic rocks of dacite, andesite, basaltic andesite, and basalt composition. Felsic (andesite, dacite, and rhyodacite) and basic rocks (basalt, basaltic andesite and andesite) commonly occur in successive layers. This alternation along with multiple occurrences of various types of tuffs suggests prolonged and successive magmatic activity during Eocene-Oligocene in NW Iran. Fractional crystallization has been the most important factor controlling geochemical characteristics of the magma. However, absence of linear correlations on variation diagrams of some immobile elements (such as Al2O3, TiO2, P2O5 and Ga) and poorly-developed trends on variation diagrams of Na2O, MgO, MnO, CaO, Fe2O3, Nb, Nd, Y, La, Ce, Th, Hf, Sc, Zn, V, Ni and Co versus SiO2 indicate that, other than crystal (olivine, pyroxene, plagioclase, biotite, hornblende, zircon, monazite and apatite) fractionation, crustal processes (such as assimilation) have also affected the chemistry of the Mendejin magma. It appears that the basic magma has originated from the mantle whereas the felsic magma resulted from modification in the mantle-derived magma by assimilation in an active continental margin.  相似文献   

8.
《International Geology Review》2012,54(12):1445-1461
We present zircon U–Pb ages, Hf isotopes, and whole-rock geochemistry of the Xiaochuan gneissic granite intrusion, SE China, to constrain its petrogenesis and provide insights into early crustal evolution of the Cathaysia Block. LA-ICP-MS zircon U–Pb dating of a representative sample yields a weighted mean 206Pb/207Pb age of 1839 ±16 Ma, interpreted as the emplacement age of the Xiaochuan granite. Zircons have ?Hf(t) values ranging from –8.1 to 2.7 and T DM2 model ages from 2.23 to 3.03 Ga. The granites are strongly peraluminious (A/CNK = 1.14–1.41), with relatively high FeOt, TiO2, and CaO/Na2O, and low CaO, Al2O3/TiO2, and Rb/Sr values. In addition, they show strongly negative Ba, Sr, Nb, and Ta and positive Th and Pb anomalies in the primitive mantle-normalized spider diagram, similar to other Cathaysia Palaeoproterozoic S-type granites. The geochemical and Hf isotopic signatures suggest that the Xiaochuan gneissic granites were generated by partial melting of Archaean crustal materials in an intraplate extensional setting. Our results, combined with existing geochronological data, further demonstrate that the Wuyishan terrane is underlain by Palaeoproterozoic crystalline basement.  相似文献   

9.
Major element, Sr isotope and trace element data for 16 elements are reported for various weathered zones in three submarine basalt pillows. During the initial stages of alteration, it appears that SiO2, Al2O3, CaO, S, and Ga are lost from the basalt, whereas Fe2O3, total Fe, MnO, K2O, H2O, Cl, B, Rb, and Cs increase. Sr87/Sr86 ratios also increase during weathering. MgO, Na2O, P2O5, Ba, Ni and Cu show significant (10–50%) but less consistent changes. TiO2, Zr, Sr and V show only minor changes (<7%). Zn, Cr, Co, Y and Nb show no changes outside experimental error.  相似文献   

10.
<正>REE fractionation during the weathering of dolomite has been recognized for decades.A regolith profile on dolomite in southwest Yunnan of China was selected to investigate the behaviors of REE during weathering.The weathering of dolomite is divided into two stages:the pedogenesis stage and soil evolution stage,corresponding to the saprolites and soils respectively in the regolith profile. SiO_2,TiO_2,P_2O_5,Zr,Hf,Nb and Ta were immobile components during the weathering by and large, while Al_2O_3,K_2O and Fe_2O_3 were lost during the soil evolution stage in the physical form(clay minerals probably).REE were fractionated during the whole weathering of dolomite.The field weathering profile and the lab acid-leaching experiments on dolomite indicate that MREE were enriched clearly relative to other REE during the pedogenesis stage in a "capillary ascending-adsorption" mechanism, but they did not fractionate clearly in the soil evolution stage.REE were lost and accumulated in the weathering front of dolomite during the soil evolution stage in a "physical-chemical leaching" mechanism.  相似文献   

11.
丹池成矿带是我国重要锡多金属成矿带,过去对丹池成矿带成岩成矿研究主要集中在大厂矿田及五圩矿田,而对丹池成矿带北部的芒场矿田岩浆作用时代、源区特征及其成矿性缺少分析。芒场矿田岩浆活动强烈,发育隐伏斑状花岗岩及有关的花岗斑岩脉和隐伏细粒花岗斑岩及有关的白云母花岗斑岩脉。本文分析花岗斑岩脉U-Pb年龄及花岗斑岩脉和白云母花岗斑岩脉主、微量元素组成,以探讨岩浆活动时代、岩浆源区特征及其成矿潜力。芒场矿田花岗斑岩脉锆石U-Pb年龄为89.1±0.9Ma (MSWD=0.9),和丹池成矿带内大厂矿田岩浆活动时代相近,表明丹池成矿带岩浆活动时代都发生于90Ma左右。白云母花岗斑岩脉具高A/CNK比值(2.69～2.88),含高铝硅酸盐矿物白云母及在Th-Rb图上沿S型花岗岩趋势线分布,和大厂矿田S型黑云母花岗岩的特征基本一致,表明其主要为S型花岗岩。花岗斑岩脉形成时代晚于白云母花岗斑岩脉,但其具有更低的SiO_2含量和更高的MgO、Fe_2O_3~T、CaO和TiO_2含量,且在SiO_2与TiO_2、Fe_2O_3~T、Al_2O_3和P_2O_5关系图中分布于不同区域,没有线性变化关系,显示两者不是同一岩浆结晶分异演化形成的,而为不同沉积变质岩部分熔融形成的。白云母花岗斑岩脉富Al_2O_3、K_2O、Rb、Cs、Sn、W、Nb和Ta,在Rb/Ba-Rb/Sr图上位于富粘土源区,为强风化作用形成的富粘土质富稀有金属源区部分熔融形成的产物。华南西部基底发育经强风化作用形成的富粘土质富稀有金属元素沉积变质源区,为华南西南缘大规模锡矿床的形成提供了物质基础。  相似文献   

12.
Geological, petrological and geochemical studies indicated that there are two distinct types of granitoid rocks: older quartz diorites to granodiorite assemblage and younger granitoids, the latter occurring in two phases. The older granitoids have a meta-aluminous chemistry and a calc-alkaline character, with high MgO, Fe2O3, TiO2, CaO, P2O5, Sr and low SiO2, K2O, and Rb. Their major and trace elements data, together with low 87Sr/ 86Sr ratios (0.7029±0.0008) are indicative of I-type affinities. The second-...  相似文献   

13.
Sandstones and shales from the Upper Neoproterozoic (UN) succession in the Central Iberian Zone (CIZ) show parallel REE patterns and relatively restricted and similar ranges and average values of some element ratios such as Al2O3/TiO2, Ti/Nb, Eu/Eu*, (La/Yb)n, (Gd/Yb)n and Th/U. This remarkable geochemical homogeneity for related medium- and fine-grained rocks is unusual, and strongly suggests a recycled source area. However, the Lower Cambrian (LC) equivalent rocks are, in general terms, geochemically less mature, more heterogeneous and more fractionated. Their average REE patterns are practically coincident, probably as a consequence of REE redistribution related to the reworking of sediments during a stage of sea level fall in Lower Cambrian times. Ti and Zr abundances, chemical index of alteration (CIA) values and element ratios such as Al2O3/TiO2, K/Rb, Ti/Nb and Rb/Zr can be used for discriminating purposes between the UN and LC siliciclastic rocks. Detrital zircons from a UN and a LC sandstone display morphological differences. However, U-Pb data are discordant and cannot be interpreted in a straightforward manner. Nevertheless, age data are compatible with a model in which the continent of Gondwana would have supplied zircons, showing a bimodal age distribution, in variable proportions to the respective sandstone units.  相似文献   

14.
Extremely fractionated basaltic to ferrobasaltic amphibolites and granulites comprise two spatially associated mafic tholeiitic suites (?deformed sills) within the Early Proterozoic Oonagalabi basement gneiss complex, Harts Range, Central Australia. The metatholeiites are characterised by high to very high FeO, TiO2 and P2O5 contents, and variable depletion in CaO and Al2O3. Despite similar Zr/Nb ratios, the rocks from the two suites show different degrees of enrichment in LREE and other “immobile” incompatible elements. The basaltic melts which were parental to the two mafic suites were not comagmatic and the rocks cannot be related simply by fractionation of realistic assemblages of low-pressure fractionating phases. The data suggest that primary basaltic liquids for the two suites were derived by different degrees of partial melting from essentially similar undepleted mantle source regions. Clinopyroxene in the residual mantle assemblage controlled the composition of the segregating melt at lower degrees of melting. The ferrobasaltic compositions imply long residence times for the basaltic magmas in shallow-level differentiating tholeiitic sills and/or magma chambers in a mature propagating rift environment. High-grade (granulite facies) metamorphism, and subsequent restricted metasomatic reequilibration of the mafic rocks with interlayered migmatitic and quartzofeldspathic gneisses, have affected only abundances of certain highly-smobile elements (e.g. K2O and Rb), resulting in the partial disruption of inter-element correlations. However, the geochemical data do not indicate any large-scale depletion of large ion lithophile elements (LILE) in the Oonagalabi gneiss complex.  相似文献   

15.
Sixteen alluvial and terrace soils from Japan and Thailand were separated into six fractions ; an amorphous sesquioxide and combined organic matter fraction, crystalline sesquioxides, clay, silt, fine sand and coarse sand. Content of ten major and minor elements in these six fractions was analyzed; SiO2, A12O3, Fe2O3, MgO, CaO, K2O, TiO2, Rb2O and SrO were determined by X-ray fluorescence spectrometry, and Na2O was determined by neutron activation analysis. The clay, silt, fine sand and coarse sand mineralogy were estimated semi-quantitatively by X-ray diffraction methods.We propose three indices of geochemical maturity for the soils and test their usefulness as measures of the degree of weathering. Three concomitant factors are proposed to measure the relative resistate, hydrolyzate and oxidate nature of the major elements in the soils.  相似文献   

16.
The Upper Neoproterozoic-Lower Cambrian sedimentary succession in the Central Iberian Zone has recently been divided into 12 sedimentary units (I to XII). Units I to IV are of Late Neoproterozoic age, and units V to XII are Early Cambrian.Throughout the stratigraphic section, shales with similar ranges of SiO2 and Al2O3 have TiO2 and Zr contents that are coupled and vary gradually from the bottom (unit I, TiO2 = 1.0-1.1%, Zr = 245-287 ppm) to the top (unit XII, TiO2 = 0.74-0.86%, Zr = 141-192 ppm). These two parameters clearly distinguish Upper Neoproterozoic from Lower Cambrian compositions, as do certain elemental ratios (Al2O3/TiO2, Rb/Zr, Nb/Ti), which vary from low values at the bottom of the section to high at the top. However, other elements (the rare earth elements [REEs], Y) do not fit this general trend, with heavy REEs and Y showing extreme concentrations in some Lower Cambrian units, which also have negative Ce anomalies.Units I to III and units XI to XII have uniform TDM neodymium model ages (∼1.1 and 1.7 Ga, respectively), but the units between these two groups have erratic values between 1.4 Ga (unit VII) and 3.4 Ga (unit VIII). Thus, the bottom and top units have neodymium isotope ratios that indicate the presence of two source compositions: a composition that records a juvenile contribution younger than 1.1 Ga and a composition mainly derived from an old basement. Some samples from Lower Cambrian units have disturbed REE abundances and neodymium isotope ratios that are attributed to extensive chemical alteration that resulted in REE and Y redistribution. This alteration probably affected the material now preserved as unit IV during a period of relative sea level fall at the end of the Late Neoproterozoic. Both elemental and isotopic results support the suggestion that the Upper Neoproterozoic-Lower Cambrian stratigraphic section records an inverse stratigraphy of a source hinterland composed of a cover sequence of relatively juvenile crustal materials underlain by an older basement. Through time, the deeper crust gradually increased its contribution to the sediments in the basin from Late Neoproterozoic to Lower Cambrian times. These results are compatible with data from many other European zones.  相似文献   

17.
Recently measured high gamma ray values in the Yanchang Formation of the Upper Triassic in the Ordos Basin have added an interesting and controversial twist to the study of the formation’s uranium enrichment and genesis. High uranium and thorium contents in the tuffaceous layer cause high gamma ray values in the Yanchang Formation. Petrographic studies, major elements, rare earth elements (REEs), and trace elements have been systematically analyzed to determine the composition, geochemical environment, and diagenetic processes of the layer. The observed color of the tuffaceous layer in the study area varies from yellow to yellowish brown. The tuff consists of matrix supported with sub-rounded to sub-angular lithic fragments. These lithic fragments probably derived from pre-existing rocks and incorporated into the tuffaceous layer during volcanic eruption. Quartz, plagioclase, and biotite were observed in well to poorly sorted form, in addition to framboidal pyrite and organic laminae. Measured ratios of SiO2/Al2O3 ranged from 3.277 to 6.105 with an average of 3.738. The ratio of TiO2/Al2O3 varied from 0.037 to 0.201 with an average of 0.061, indicating that the sediments of the tuffaceous layer originated from an intermediate magma. REE distribution patterns show sharp negative Eu anomalies, indicating a reducing environment, which is suitable for uranium deposition. A reducing environment was confirmed by black shale in the base of the Yanchang Formation. Such black shale has high organic matter content that can take kerogene from mudstone and provide a reducing environment for uranium enrichment in the tuffaceous layer. Moreover, negative Eu anomalies and the REE patterns indicate a subduction-related volcanic arc environment as the magma source of the tuffaceous layers. High values of Rb, Ba, and Sr might be the result of fluid phase activities; low values of Hf and Eu indicate the involvement of crustal material during diagenesis of the tuff. Discrimination diagrams (Th/Yb vs Ta/Yb, Th/Hf vs Ta/Hf) suggest an active continental margin as the tectonic setting of source volcanoes. Plots of Nb versus Y, Rb versus Y + Nb, TiO2 versus Zr, and Th/Yb versus Nb/Yb of the tuffaceous content point to calc-alkaline continental arc-related magmatism. We concluded that uranium enrichment in the tuffaceous layer was supported by oxidation–reduction.  相似文献   

18.
Discrimination diagrams have been developed that source Egyptian basaltic artefacts using whole‐rock major element geochemistry. These include K2O versus SiO2, TiO2 and P2O5 against MgO/Fe2O3t (total Fe as Fe2O3), and a discriminant analysis diagram using SiO2, Fe2O3t, CaO, and MnO. A complementary set of diagrams uses easily obtained trace element data (Nb/Y versus Zr/Nb; Zr [ppm] versus Rb/Sr; TiO2 [wt % volatile free] versus V; and Cr [ppm] versus Zr/Y) to determine the bedrock sources. These diagrams have been applied to seven First Dynasty basalt vessels (Abydos), two Fourth Dynasty basalt paving stones (Khufu's funerary temple, Giza), and two Fifth Dynasty paving stones (Sahure's complex, Abu Sir). They show that the bedrock source for all the artefacts was the Haddadin flow in northern Egypt. Multidimensional scaling and cluster analysis applied to the whole‐rock data (major elements and trace elements together) and previously published mineral fingerprinting studies confirm these results. Comparing mineral versus whole‐rock fingerprinting techniques, a major advantage of the former is the small sample size required (0.001 g compared to ≥ 0.1 g). Analytical costs are similar for both methods assuming that a comparison (bedrock) database can be assembled from the literature. For most archaeological problems, a whole‐rock bedrock database is more likely to exist than a mineral database, and whole‐rock analyses on artefacts will generally be easier to obtain than mineral analyses. Whole‐rock fingerprinting may be more sensitive than mineral‐based fingerprinting. Thus, if sample quantity is not an issue, whole‐rock analysis may have a slight cost, convenience, and technical advantage over mineral‐based methods. Our results also emphasize that the Egyptians cherished their Haddadin basalt flow and used it extensively and exclusively for manufacturing basalt vessels and paving stones for at least 600 years (∼3150 B.C. to 2500 B.C., approximate ages of the vessels and Abu Sir paving stones, respectively). © 2001 John Wiley & Sons, Inc.  相似文献   

19.
The Dajia Salento-type bauxite deposit in western Guangxi is hosted within the Quaternary ferrallitic soil profile, and it formed via breaking up, weathering and oxidizing of Permian bauxite orebodies occurring as a semi-continuous layer in the upper Permian. Mineralogical analyses reveal that diaspore, hematite and kaolinite are the major minerals in bauxite ores with small amounts of anatase, chamosite, gibbsite, goethite, illite, zircon, quartz and pyrite. The ore texture and mineral assemblage reveal that the depositional/diagenetic environment of the Dajia bauxite was much close to phreatic environment. Both the ore texture and the morphology of zircon grains also indicate that most of the bauxitic soils were transported a short distance. Diaspore is suggested to be non-metamorphic in origin and mainly formed in a reducing condition of diagenetic environment, while kaolinite is the product of the in situ epigenetic replacement of alumina in diaspore by dissolved silica. Geochemical analyses indicate that Al2O3, Fe2O3, SiO2 and TiO2 are the main components of the bauxite ores and trace elements such as Zr, Hf, Nb, Ta, Th and U were enriched during the bauxitization process. Simultaneously, Zr vs. Hf and Nb vs. Ta show a high correlation. Geochemical indices such as Zr/Hf, Nb/Ta and Eu/Eu* (among others) denote that the magmatic rocks related to the Emeishan plume in western Guangxi and the carbonates in the underlying Maokou Formation provided the main sources of material for the bauxite ores.  相似文献   

20.
Granitoid rocks of the compositionally zoned Late Cretaceous Toulumne Intrusive Suite in the central Sierra Nevada, California, have initial87Sr/86Sr values (Sri) and143Nd/144Nd values (Ndi) that vary from 0.7057 to 0.7067 and from 0.51239 to 0.51211 respectively. The observed variation of both Sri and Ndi and of chemical composition in rocks of the suite cannot be due to crystal fractionation of magma solely under closed system conditons. The largest variation in chemistry, Ndi, and Sri is present in the outer-most equigranular units of the Tuolumne Intrusive Suite. Sri varies positively with SiO2, Na2O, K2O, and Rb concentrations, and negatively with Ndi, Al2O3, Fe2O3, MgO, FeO, CaO, MnO, P2O5, TiO2, and Sr concentrations. This covariation of Sri, Ndi and chemistry can be modeled by a process of simple mixing of basaltic and granitic magmas having weight percent SiO2 of 48.0 and 73.3 respectively. Isotopic characteristic of the mafic magma are Sri=0.7047, Ndi=0.51269 and 18O=6.0, and of the felsic magma are Sri=0.7068, Ndi=0.51212 and 18O=8.9. The rocks sampled contain from 50 to 80% of the felsic component. An aplite in the outer equigranular unit of the Tuolumne Intrusive Suite apparently was derived by fractional crystallization of plagioclase and hornblende from magma with granudiorite composition that was a product of mixing of the magmas described above. Siliceous magmas derived from the lower crust, having a maximum of 15 percent mantle-derived mafic component, are represented by the inner prophyritic units of the Tuolumne Intrusive Suite.  相似文献   

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