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1.
Investigations in quarry exposures in the Asheldham Gravel and related deposits of southeast Essex are described. Section logging, mapping and borehole investigations are supported by clast lithological, heavy and clay mineralogical determinations. The sediments are derived from reworking of local Thames basin materials, fine sediment being predominantly from the London Clay. The sequence is shown to represent an aggradation that began as the fluvial infilling of the River Medway valley. The River Thames, diverted into this valley by glaciation further west, overwhelmed the Medway, reworking the deposits. The valley was subsequently drowned and fine laminated lake sediment was initially deposited. This was during a period when the valley was drowned by the glacial lake ponded in the southern North Sea basin by the Anglian/Elsterian ice sheet. Progradation by a braid-delta complex advanced along the valley and subsequently fluvial deposition returned. Valley widening and straightening accompanied the delta progradation. The deposits were dissected by deep fluvial valleys infilled by Hoxnian interglacial sediments. The Asheldham Gravel is therefore placed in the Anglian/Elsterian Stage.  相似文献   
2.
HEINZ LANGE 《Sedimentology》1982,29(3):427-431
Chlorite in the Atlantic sediments is predominantly derived from the Atlas Mountains, kaolinite originates in the southern Sahara and Sahel zone. These minerals may be used to reconstruct the tracks of two superimposed wind systems (Trade Winds and Harmattan Wind). A modified method for determining relative abundances of chlorite and kaolinite is presented.  相似文献   
3.
Chemical, spectrographic, and isotopic analyses are presentedfor the Franzfontein alkali granite and constituent minerals.This rock has the chemical character of granties produced byliquid crystal equilibrium. Dated at 1, 700?70m.y. by the constituentzircon, its crystallization formed part of a major period (theHuabian episode) of batholithic granite emplacement in northernSouth-West Africa. The occurrence of these crystalline rocksin the core of the Huab anticline defines the maximum possibleage of the overlying Otavi Facies sediments, precluding theircorrelation with the Transvaal System of South Africa. The imprint of the Damara metamorphism (Damaran episode) isreflected in the Sr/Rb age (560?30 m.y.) obtained for the biotite:the inversion of biotite to stilpnomelane and chlorite probablyrepresents the mineralogical effects of that metamorphis. Isotopicdata indicate that changes in the relative concentrations ofRb and Sr differed significantly in plagioclase and microcline;such data from feldspars in metamorphic rocks should, therefore,be interpreted with caution.  相似文献   
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Abstract— We report the elemental and isotopic composition of the noble gases as well as the chemical abundances in pyroxene, maskelynite/mesostasis glass, and bulk material of Shergotty and of bulk samples from Chassigny and Yamato 793605. The 40K-40Ar isochron for the Shergotty minerals yields a gas retention age of 196 Ma, which is, within errors, in agreement with previously determined Rb-Sr internal isochron ages. Argon that was trapped at this time has a 40Ar/36Ar ratio of 1100. For Chassigny and Y-793605, we obtain trapped 40Ar/36Ar ratios of 1380 and 950, respectively. Using these results and literature data, we show that the three shergottites, Shergotty, Zagami, and QUE 94001; the lherzolites ALH 77005, LEW 88516, and Y-793605; as well as Chassigny and ALH 84001 contain a mixture of Martian mantle and atmospheric Ar; whereas, the trapped 40Ar/36Ar ratio of the nakhlites, Nakhla, Lafayette, and Governador Valadares cannot be determined with the present data. We show that Martian atmospheric trapped Ar in Martian meteorites is correlated with the shock pressure that they experienced. Hence, we conclude that the Martian atmospheric gases were introduced by shock into the meteoritic material. For the Shergotty minerals, we obtain 3He-, 21Ne-, and 38Ar-based cosmic-ray exposure ages of 3.0 Ma, and for the lherzolite Y-793605, 4.0 Ma, which confirms our earlier conclusion that the lherzolites were ejected from Mars ~1 Ma before the shergottites. Chassigny yields the previously known ejection age of 11.6 Ma.  相似文献   
6.
Abstract— Experiments on a Martian basalt composition show that Dv augite/melt is greater than Dv pigeonite/melt in samples equilibrated under the same fO2 conditions. This increase is due to the increased availability of elements for coupled substitution with the V3+ or V4+ ions, namely A1 and Na. For this bulk composition, both A1 and Na are higher in concentration in augite compared with pigeonite; therefore more V can enter augite than pigeonite. Direct valence state determination by XANES shows that the V3+ and V4+ are the main V species in the melt at fO2 conditions of IW‐1 to IW+3.5, whereas pyroxene grains at IW‐1, IW, and IW+1 contain mostly V3+. This confirms the idea that V3+ is more compatible in pyroxene than V4+. The XANES data also indicates that a small percentage of V2+ may exist in melt and pyroxene at IW‐1. The similar valence of V in glass and pyroxene at IW‐1 suggests that V2+ and V3+ may have similar compatibilities in pyroxene.  相似文献   
7.
Numerous minette dykes intersect the Precambrian crystallinebasement of Schirmacher Oasis, East Antarctica. This study presentsnew Sr, Nd, Pb and O isotope data for 11 minette samples fromfour different dykes. The samples are characterized by relativelyhigh 87Sr/86Sr (0·7077–0·7134), 207Pb/204Pb(15·45–15·55) and 208Pb/204Pb (37·8–39·8),combined with low 143Nd/144Nd (  相似文献   
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9.
Abstract– Paired meteorites Graves Nunatak 06128 and 06129 (GRA) represent an ancient cumulate lithology (4565.9 Ma ± 0.3) containing high abundances of sodic plagioclase. Textures and stable isotope compositions of GRA indicate that superimposed on the igneous lithology is a complex history of subsolidus reequilibration and low‐temperature alteration that may have extended over a period of 150 Myr. In GRA, apatite is halogen‐rich with Cl between 4.5 and 5.5 wt% and F between 0.3 and 0.9 wt%. The Cl/(Cl+F+OH) ratio of the apatite is between 0.65 and 0.82. The Cl and F are negatively correlated and are heterogeneously distributed in the apatite. Merrillite is low in halogens with substantial Na in the 6‐fold coordinated Na‐site (≈2.5%) and Mg in the smaller octahedral site. The merrillite has a negative Eu anomaly, whereas the apatite has a positive Eu anomaly. The chlorine isotope composition of the bulk GRA leachate is +1.2‰ relative to standard mean ocean chloride (SMOC). Ion microprobe chlorine isotope analyses of the apatite range between ?0.5 and +1.2‰. Textural relationships between the merrillite and apatite, and the high‐Cl content of the apatite, suggest that the merrillite is magmatic in origin, whereas the apatite is a product of the interaction between merrillite and a Cl‐rich fluid. If the replacement of merrillite by apatite occurred at approximately 800 °C, the fluid composition is f(HCl)/f(H2O) = 0.0383 and a HCl molality of 2.13 and f(HCl)/f(HF) = 50–100. It is anticipated that the calculated f(HCl)/f(H2O) and a HCl molality are minimum values due to assumptions made on the OH component in apatite and basing the calculations on the apatite with the lowest XCl. The bulk δ37Cl of GRA is a >2σ outlier from chondritic meteorites and suggests that parent body processes resulted in fractionation of the Cl isotopes.  相似文献   
10.
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