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1.
The ~750 km2 Dayman dome of the Late Cretaceous Suckling‐Dayman massif, eastern Papua New Guinea, is a domed landform that rises to an elevation of 2850 m. The northern edge of the dome is a fault scarp >1000 m high that is now part of an active microplate boundary separating continental crust of the New Guinea highlands from continental and oceanic crust of the Woodlark microplate. Previous work has shown that a parallel belt of eclogite‐bearing core complexes north‐east of the Dayman dome were exhumed from up to 24–28 kbar in the last few millions of years. The remarkably fresh and lightly eroded scarp of the Dayman dome exposes shallowly‐dipping mylonitic (S1) metabasite rocks (500 m thick) on the northern flank of Mount Dayman. Field relationships near the base of this scarp show a cross cutting suite of ductile and brittle meso‐structures that includes: (i) rare ductile S2 folia with a shallowly ESE‐plunging mineral elongation lineation defined by sodic‐calcic blue amphibole; (ii) narrow steeply‐dipping ductile D2 shear zones; and (iii) semi‐brittle to brittle fault zones. Pumpellyite‐actinolite facies assemblages reported by previous workers to contain local aragonite, lawsonite and/or glaucophane are found in the core of the complex at elevations greater than 2000 m. These assemblages indicate peak metamorphic pressures of 6–9.5 kbar, demonstrating exhumation of the core of the Dayman dome from depths of 20–30 km. The S1 metamorphic mineral assemblage in metabasite includes actinolite‐chlorite‐epidote‐albite‐quartz‐calcite‐titanite, indicative of greenschist facies conditions for the main deformation. New mineral equilibria modelling suggests that this S1 assemblage evolved at 5.9–7.2 kbar at ~425 °C. Modelling variable Fe3+ indicates that the sodic‐calcic blue amphibole (D2) formed under a higher oxidation state compared with the S1 assemblage, probably at <4.5 kbar. A SE‐dipping, Mio‐Pliocene sedimentary sequence (Gwoira Conglomerate) forms a hangingwall block juxtaposed by low‐angle fault contact with the metabasite footwall. Prehnite‐bearing D3 brittle fault zones separate the two blocks and likely accommodated the final exhumation of the S1 greenschist facies assemblage in the footwall. These results indicate that the extensive Mt Dayman fault surface coincides with a domed S1 greenschist facies foliation that was last active at >20 km depth. Exhumation of this foliation must therefore be controlled by brittle faults of the active microplate boundary that are largely not observed in the study area. The structural record of the final exhumation of the Dayman dome to the surface was likely lost as a result of erosion, poor exposure or wide spacing of semi‐brittle to brittle fault zones.  相似文献   
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山东沂水太古宙麻粒岩区年代学研究成果简介   总被引:2,自引:0,他引:2  
本文以详细研究本区麻粒岩-斜长角闪岩等表壳岩的岩石学、地球化学和 Sm-Nd 同位素定年为重点。所取得的成果,对华北陆台古老地层的分布和古构造格局的探索提供了实际资料。  相似文献   
4.
元素地球化学研究结果表明,苍山变质带内发育两类正变质基性岩:一类为形成于富集型MORB构造环境的变拉斑玄武岩,另一类为形成于板内构造环境的变碱性玄武质岩墙,Sm-Nd同位素体系研究表明,变拉斑玄武岩形成于晚古元古代至中元古代(2.0-1.4G a );变碱性玄武质岩墙形成于中新元古代(1.3-0.8Ga),已发表的Sm-Nd等时线年龄(2408Ma)其Sm/Nd比植变化很小,故没有实际的地质意义。  相似文献   
5.
在山东太古宙沂水杂岩的变基性岩类中首次获得的Sm-Nd全岩等时线同位素年龄为2997Ma,证实了山东中部的郯庐断裂带中有中太古代麻粒岩相表壳岩存在。沂水杂岩的岩石组合主要有二辉斜长麻粒岩、二辉斜长片麻岩、二辉铁英岩(少量)、二辉斜长角闪岩和紫苏花岗岩类等,它们组成了山东最老的汞丹山地块,其时代大致相当于胶东群,但层位可能更为偏下。沂水杂岩为高角闪岩相至麻粒岩相。变基性岩的原岩相当低钾拉斑玄武岩,稀土配分具有较平坦型和轻稀土富集型两种模式。岩石的ε_(Nd)(t)值为+3.8±0.3,物源来自亏损(上)地幔。它与华北陆台北缘麻粒岩相中部分岩石的岩性十分相似,表明其源区的化学特征相似,但主体的稀土模式有所不同,说明太古宙不同地区相似岩石地球化学的不均匀性。  相似文献   
6.
保山地体寒武纪基性火山岩及其大地构造意义   总被引:2,自引:1,他引:1  
保山地体位于青藏高原东南缘。有关保山地体的岩浆作用研究大多集中在中生代及新生代,针对古生代岩浆作用的讨论较少。对云南省保山邦迈地区蒲满哨群中变质基性岩的锆石U-Pb年代学、地球化学及Sm-Nd同位素组成进行了研究。这些变质基性岩可分为2组:一组为斜长角闪岩,另一组为黑云斜长角闪岩。锆石U-Pb测年结果表明,斜长角闪岩的形成时代为536.7Ma,黑云斜长角闪岩的形成时代为532.0Ma。地球化学特征显示,斜长角闪岩的原岩为玄武安山岩,黑云斜长角闪岩的原岩为碱性玄武岩。稀土和微量元素配分曲线及多种构造环境判别图解显示,二者分别具有富集型大洋中脊玄武岩和洋岛玄武岩的地球化学特征。结合区域大地构造背景认为,保山地体邦迈变质基性岩为洋脊俯冲的产物。在新元古末期—早古生代,保山地体与拉萨地体、喜马拉雅地体等类似,皆位于冈瓦纳大陆边缘,且共同经历了增生造山过程。  相似文献   
7.
Chlorite is a common sheet silicate that occurs in various lithologies over a wide grade range involving diagenesis and low‐grade metamorphism. Thus, the reaction progress of chlorite offers a unique opportunity for direct correlation of zonal classification of metasedimentary rocks based on illite crystallinity with metabasite mineral facies. To provide such correlation, chlorite crystallinity indices, apparent mean crystallite sizes and lattice strains, crystallite size distributions and compositions of chlorite from coexisting metapelites and metabasites were determined by X‐ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), analytical electron microscopy (AEM) and electron microprobe (EMP) methods. Samples were from Palaeozoic and Mesozoic formations of the Bükkium (innermost Western Carpathians, Hungary) that underwent Alpine (Cretaceous) orogenic metamorphism. Metapelites range in grade from late diagenesis to epizone, whereas metabasites vary from prehnite–pumpellyite through pumpellyite–actinolite to greenschist facies. Despite significant differences in composition, mineral assemblages and textures, reaction progress, as measured in part by chlorite crystallinity, in metapelites paralleled that in metabasites. Chlorite crystallinity and mean crystallite size increase and the proportion of mixed layers in chlorite decreases, whereas the calculated lattice strain does not change significantly with increasing metamorphic grade. Similar trends, but (especially at higher grades) significant differences, were found in mean crystallite size values using various methods for XRD line profile analyses. The increase in crystallite size with increasing grade was demonstrated also by direct TEM measurements on ion‐milled whole‐rock samples, but with a larger scatter of data at higher grades. In spite of the different kinds of mixed layering in chlorite (Mg‐rich smectitic, mostly random, local corrensite‐like units in metabasites, and Fe‐rich berthierine and dioctahedral smectite in metapelites), XRD‐calculated and TEM‐measured parameters were found to be reliable tools for measuring reaction progress and metamorphic grade of the same degree in both lithotypes.  相似文献   
8.
Recently published activity–composition (ax) relations for minerals in upper amphibolite‐ and granulite facies intermediate and basic rocks have expanded our ability to interpret the petrological evolution of these important components of the lower continental crust. If such petrological modelling is to be reliable, the abundances and compositions of phases calculated at the interpreted conditions of metamorphic equilibration should resemble those in the sample under study. Here, petrological modelling was applied to six granulite facies rocks that formed in different tectonic environments and reached different peak metamorphic pressure–temperature (PT) conditions. While phase assemblages matching those observed in each sample can generally be calculated at PT conditions that approximate those of peak metamorphism, a consistent discrepancy was found between the calculated and observed compositions of amphibole and clinopyroxene. In amphibole, Si, Ca and A‐site K are underestimated by the model, while Al and A‐site Na are overestimated; comparatively, in clinopyroxene, Mg and Si are generally underestimated, while Fe2+ and Al are typically overestimated, compared to observed values. One consequence is a reversal in the Fe–Mg distribution coefficient (KD) between amphibole and clinopyroxene compared to observations. Some of these mismatches are attributed to the incorrect partitioning of elements between the predicted amphibole and clinopyroxene compositions; however, other discrepancies are the result of the incorrect prediction of major substitution vectors in amphibole and clinopyroxene. These compositional irregularities affect mineral modal abundance estimates and in turn the position and size (in PT space) of mineral assemblage fields, the effect becoming progressively more marked as the modal abundance of hornblende increases; hence, this study carries implications for estimating PT conditions of high‐temperature metabasites using these new ax relations.  相似文献   
9.
The geochemistry of two deerite‐bearing meta‐ironstones from the Emo Metamorphics of Papua New Guinea suggests that they were deposited as metalliferous cherts enriched in manganese and iron by hydrothermal exhalative activity in an ocean ridge system. Subsequent blueschist facies metamorphism resulted in the formation of the assemblage deerite‐quartz‐albite‐iron oxides‐alkali amphiboles‐spessar‐tine‐stilpnomelane‐apatite, with calcium‐manganese carbonates in one specimen. Assemblages in associated metabasites suggest P‐T conditions of 7 kb at 320°C, which overlap with the P‐T field defined by one of the meta‐ironstones. Oxygen fugacity was probably an important control in determining variations in mineralogy and mineral chemistry. Preliminary data on the trace element geochemistry of associated metabasites are consistent with an ocean ridge environment for the formation of the meta‐ironstones.  相似文献   
10.
Orthopyroxene‐free garnet + clinopyroxene + plagioclase ± quartz‐bearing mineral assemblages represent the paragenetic link between plagioclase‐free eclogite facies metabasites and orthopyroxene‐bearing granulite facies metabasites. Although these assemblages are most commonly developed under P–T conditions consistent with high pressure granulite facies, they sometimes occur at lower grade in the amphibolite facies. Thus, these assemblages are characteristic but not definitive of high pressure granulite facies. Compositional factors favouring their development at amphibolite grade include Fe‐rich mineral compositions, Ca‐rich garnet and plagioclase, and Ti‐poor hornblende. The generalized reaction that accounts for the prograde development of garnet + clinopyroxene + plagioclase ± quartz from a hornblende + plagioclase + quartz‐bearing (amphibolite) precursor is Hbl + Pl + Qtz=Grt + Cpx + liquid or vapour, depending on whether the reaction occurs above or below the solidus. There are significant discrepancies between experimental and natural constraints on the P–T conditions of orthopyroxene‐free garnet + clinopyroxene + plagioclase ± quartz‐bearing mineral assemblages and therefore on the P–T position of this reaction. Semi‐quantitative thermodynamic modelling of this reaction is hampered by the lack of a melt model and gives results that are only moderately successful in rationalizing the natural and experimental data.  相似文献   
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