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ABSTRACT Thirty clay-rich horizons from the Wenlock and Ludlow Series of the Welsh Borderland were analysed to investigate their mineralogy and possible origins. Two mineralogical assemblages were determined: an assemblage of illite-smectite and kaolinite of volcanic origin which was associated in many samples with an assemblage of illite and chlorite of detrital origin. Immobile chemical discriminants (Zr/TiO2 versus Nb/Y) infer an originally rhyolitic ash composition with a possible temporal progression, from the Wenlock to Ludlow, to more differentiated compositions. The thin nature of the bentonites and lack of juxtaposed subduction related calc-alkaline magmatism suggests that the tuffs were derived from distant explosive eruptions from volcanic centres, possibly in NE Europe. 相似文献
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A combined petrographical and geochemical study has been made on a per- sistent carbonate horizon from the Mansfield Marine Band, an important marker horizon in the Westphalian Coal Measures of the east Pennines. The composition of this carbonate is unusual for it normally consists of ankerite, but in some localities the carbonate is siderite and not ankerite. The position of the carbonate in the sedimentary cycle is discussed and the conclusion drawn that physicochemical conditions were suitable for the precipitation of CaC03 to occur. Furthermore the detrital material in the carbonate band continued to accumulate at a similar rate to the shales above and below the carbonate. The alteration of the CaC03 is thought to have been a diagenetic effect and the result of a change in the physicochemical environment. Variations in the concentration of dissolved sulphur species and their effect on the solubilities of iron and manganese provide an adequate mechanism to explain how CaC03 may alter to siderite on the one hand or ankerite on the other. 相似文献
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D. A. SPEARS 《Sedimentology》1976,23(5):721-725
Laminations control the fissility of a sequence of shales and mudstones from the Upper Carboniferous Coal Measures in Britain. This was established by measuring the thickness of pairs of laminations in unweathered borehole material and comparing with the thickness of shale fragments at the outcrop of the same sequence. The parallel orientation of the clay minerals is not responsible for the fissility and it could be that its importance has been overestimated. The processes responsible for the formation and preservation of the laminations will also produce a well orientated clay fabric and hence fissility and clay orientation may be indirectly related. 相似文献
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The volcanic origin of a number of major tonstein horizons has been established from mineralogical compositions and from trace elements that are quantitatively retained during diagenesis. Discriminant function analysis using the variables Ti/Al, Cr/Al, Zr/Al and Ni/Al allows the tonsteins to be classified according to original composition. Two main groups are recognized amongst the British tonsteins. Those formed from acid volcanic ash are comparable in composition with French and German tonsteins and a common source is postulated, whereas tonsteins formed from basic volcanic ash contain variable amounts of detrital sediment and are thought to originate from local eruptions. Possible lateral equivalents between tonstein horizons in Britain and elsewhere in Europe are suggested. 相似文献
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Nine Namurian clay bands retrieved from boreholes in the northern part of the Pennine Basin are, on the basis of their petrography, mineralogy and geochemistry, shown to be volcanic in origin and are therefore bentonites. The bentonites, which have a fragmental texture, are normally graded and show rare preservation of shard textures, representing vitric tuff deposits that have been altered subsequently to clay-dominated horizons. Crystals are a minor component of the bentonites, but biotite, in particular, is concentrated at the base of the beds. A clay mineral assemblage of mixed-layer illite–smectite with subordinate kaolinite identifies most of the samples as K-bentonites, but kaolinite dominates two samples that can be classed as tonsteins. Temporal variation of salinity within the depositional basin is suggested to explain these different clay assemblages. The major element geochemistry of the bentonites reflects their clay mineralogy and the compositions of diagenetic minerals present, the latter including pyrite, carbonates and hydroxyapatite. Enrichment of the bentonites in some trace elements (including Ba, Sr, Pb, Cu and Ni) can be related to the presence of the diagenetic minerals, but the extent to which the elements are added from external sources as opposed to being redistributed within the ash is unclear. Immobile trace element systematics suggest a rhyodacite/dacite composition for the original ash and derivation from the collision of plates, this being supported by evidence provided by the rare earth elements (REE) in one group of samples. However, in another group of samples, variations in REE concentrations may be caused by mobility of these elements during alteration. The chemistry of the Namurian bentonites contrasts markedly with that of the local Carboniferous volcanics but is comparable, in some respects, with one group of Westphalian tonsteins, although the latter are more rhyolitic in character. It is suggested that the Namurian bentonites and the Westphalian tonsteins of acid affinities originated from volcanic activity associated with a destructive plate margin in the Variscan externides and that the observed compositional trend may reflect magma evolution possibly related to the progressive east–west closure. 相似文献
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The Namurian black shales studied have a good palaeontological control. Pyrite, illite and organic matter are higher in the marine shales, and siderite and kaolinite are higher in the non-marine shales. The distribution of the diagenetic iron minerals is attributed to anionic activities controlled by salinity. The same control could account for the observed clay-mineral distribution by differential flocculation. The major element geochemistry closely reflects the above mineral variation. Mn and Zr are higher in the non-marine shales due to siderite and zircon respectively. Co, Cr, Rb, Y and Ba are not significantly different and a detrital source, mainly clay minerals, is suggested. In the marine shales the elements Pb, Cu, V, Ni, Sr and Zn are significantly higher. Using a discriminant function analysis the palaeosalinity groups are separated and the contribution of each element to the separation is calculated. The present element locations are thought, from correlation analysis, to be pyrite and organic matter. By analogy with experimental work and modern environments, the element enrichment is mainly attributed to reactions involving organic matter and oxyhydroxide material in environments in which salinity and slow rates of sedimentation were important factors. The element enrichment cannot be related directly to seawater concentrations, unlike some black shales, and the accumulation rates for Pb and Cu are thought to be unusually high. 相似文献
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Previous work on the mineralogy of the volcanic supra-Wyrley Yard tonstein is extended to include the opaque minerals. This has led to a better understanding of the major and trace element geochemistry of the tonstein. The complete mineral assemblage is kaolinite (dominant) with minor quartz, K-mica, zircon, apatite, pyrite, sphalerite, galena, rutile, dolomite, barytes, goethite and organic matter. Information on element location in the tonstein has been obtained by using autoradiography and fission track radiography, the electron probe and by analysing separated fractions with an optical spectrograph. This has enabled the diagenetic history of individual elements to be determined, and the composition of the tonstein to be compared with igneous material. The high concentration of Th, U, Pb, Sn, Bi, Y, Be and B in the tonstein, and the low concentration of Ti, Cr, V, Ni, Cu and Co is indicative of an acidic ash. A source in the Armorican orogenic belt is postulated, based on the contrast with the basaltic Carboniferous volcanism and also the high concentrations of Sn, Pb and Zn. 相似文献
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