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1.
碎屑金红石:沉积物源的一种指针   总被引:3,自引:2,他引:1  
简星  关平  张巍 《地球科学进展》2012,27(8):828-846
近年来,碎屑金红石的研究已成为沉积物源区分析的一个新前沿。金红石的地球化学组成,尤其是Cr,Nb,Zr等微量元素的含量,对其母岩的形成条件和所经历的地质过程都具有重要的指示意义,同时,碎屑金红石在沉积、成岩过程中表现出极高的稳定性,因而是物源分析的理想指针矿物。首先介绍金红石的矿物学和地球化学基本性质,分析不同来源的金红石典型特征,重点阐述碎屑金红石在物源分析中运用的5个方面:①金红石重矿物比值;②金红石矿物化学成分Cr-Nb判别图解;③金红石Zr含量温度计;④金红石的U-Pb和(U-Th)/He定年;⑤金红石Lu-Hf同位素。综合上述5个方面的物源分析研究,可以获取金红石的母岩类型、形成温度及后期所经历的热演化史等信息。碎屑金红石的物源研究处于起步和探索阶段,仍存在一些亟需解决的问题。  相似文献   
2.
Ilmenite in coronitic gabbros from the Bamble and Kongsberg sectors, southern Norway, is surrounded by zircons ranging in diameters from a fraction of a micrometer to 10 μm across. The zircons are inert during subsequent metamorphism (amphibolite- to pumpellyite–prehnite facies) and metasomatism (scapolitization and albitization) and can be found as trails in silicates (phlogopite, talc, chlorite, amphibole, albite, and tourmaline) in the altered rocks. The trails link up to form polygons outlining the former oxide grain boundary. This 3-dimensional framework of zircons is used to (a) recognize metasomatic origin of rocks, (b) quantify the mobility of elements during mineral replacement, (c) establish the growth direction of reaction fronts and to identify the reaction mechanism as dissolution–reprecipitation. Zircon coronas on Fe–Ti oxides have been described from a number of terrains and appear to be common in mafic rocks (gabbros and granulites) providing a tool for a better understanding of metasomatic and metamorphic reactions.  相似文献   
3.
苏北榴辉岩中金红石的微量元素地球化学特征   总被引:5,自引:7,他引:5  
本文利用电子探针分析了苏北地区三类榴辉岩中金红石的Nb、Cr和Zr含量,在Zaek et al.(2002)的金红石Nb-Cr图解中,三类榴辉岩的原岩均为镁铁质岩,但它们具有不同的地球化学特征,即(1)小焦G类金红石榴辉岩中金红石的Nb含量最低,平均值为68ppm,而其它两类榴辉岩中金红石的Nb含量较高,平均值介于192~255ppm;(2)蓝晶石榴辉岩具有极高Cr含量,均值6106ppm,而许沟P类榴辉岩中金红石的Cr含量也较高,均值1233ppm,金红石榴辉岩中金红石Cr含量最低,均值为183ppm。利用Zaek et al.(2004)提出的金红石地质温度计,计算得出许沟P类榴辉岩的金红石形成温度介于600~751℃,平均温度689℃;演马厂M类榴辉岩的金红石温度介于507~641℃,平均温度557℃;小焦G类金红石榴辉岩金红石的形成温度介于541~673℃,平均温度613℃;新扬昌G类蓝晶石榴辉岩的金红石形成温度介于541~655℃,平均温度603℃。一种可能的解释是,榴辉岩在拆返过程中退变质作用明显,流体活动强烈,导致金红石中Zr扩散丢失,金红石中Zr含量不同程度地受到角闪岩相退变质过程中再平衡作用的影响,致使计算的温度偏低。  相似文献   
4.
Neutron irradiation and post-irradiation annealing under oxidising and reducing conditions have been used to investigate H incorporation in, and the optical properties of, reduced (TiO2−x ) rutile. Optical absorption in rutile is mainly due to a Ti3+ Ti4+ intervalence charge transfer effect. The main mechanism for H incorporation in rutile involves interstitial H not coupled to other defects, which has important implications for the rate of H diffusion, and possibly also on the electrical properties of rutile. Additional minor OH absorption bands in IR spectra indicate that a small amount of interstitial H is coupled to defects such as Ti3+ on the main octahedral site, and indicates that more than one H incorporation mechanism may operate. Concentration of oxygen vacancies has a controlling influence on the H affinity of rutile.  相似文献   
5.
Zr-in-rutile thermometry in blueschists from Sifnos, Greece   总被引:1,自引:0,他引:1  
Zr-in-rutile thermometry on samples of blueschist from Sifnos, Greece, yields temperatures that reflect progressive crystallization of rutile from ca. 445 to 505°C with an analytical precision of + 18/−27 and ± 10°C using the electron microprobe and ± 1.5–3.5°C using the ion microprobe. Individual grains are generally homogeneous within analytical uncertainty. Different grains within a single sample record temperature differences as large 55°, although in most samples the range of temperatures is on the order of 25°. In several samples, Zr-in-rutile temperatures from grains within garnet are lower than temperatures from matrix grains, reflecting growth of rutile with increasing temperature of metamorphism. Although the specific rutile-producing reactions have not been identified, it is inferred that rutile grows from either continuous reaction involving the breakdown of lower grade phases (possibly ilmenite), or from pseudomorph reactions involving the breakdown of relic igneous precursors at blueschist-facies conditions. No systematic variation in rutile temperatures was observed across the blueschist belt of northern Sifnos, consistent with the belt having behaved as a coherent block during subduction.  相似文献   
6.
This paper first reports a high precision U–Pb age of 218±1.2 Ma for rutile in coesite-bearing eclogite from Jinheqiao in the Dabie Mounteins, east–central China. This work shows that the U–Pb mineral (rutile+omphacite) isochron age of 218±2.5 Ma and conventional rutile U–Pb concordia age of 218±1.2 Ma obtained by common Pb correction based on the Pb isotopic composition of omphacite in the same eclogite sample are consistent, proving that the omphacite with low U/Pb ratio (μ=2.8) can be used for common Pb correction in U–Pb dating of rutile. Oxygen isotope analysis of rutile aliquots gave the consistent δ18O values of −6.1±0.1%, demonstrating oxygen isotope homogenization in the rutile of different grains as inclusion in garnet and grain in matrix. Oxygen isotope thermometry yields temperatures of 695±35 and 460±15 °C for quartz–garnet and quartz–rutile pairs, respectively. These oxygen isotopic observations suggest that the diffusion of oxygen in rutile as inclusion in garnet is not controlled by garnet. According to field-based thermochronological studies of rutile, an estimate of the Tc of about 460 °C for U–Pb system in rutile under rapid cooling conditions (20 °C/Ma) was advised. Based on this U–Pb age as well as the reported chronological data with their corresponding metamorphic and/or closure temperature, an improved Tt path has been constructed. The Tt path confirms that the UHPM rocks in South Dabie experienced a rapid cooling following the peak metamorphism before 220 Ma and a long isothermal stage from 213 to 180 Ma around 425 °C.  相似文献   
7.
Robert L. Linnen   《Lithos》2005,80(1-4):267-280
The solubilities of columbite, tantalite, wolframite, rutile, zircon and hafnon were determined as a function of the water contents in peralkaline and subaluminous granite melts. All experiments were conducted at 1035 °C and 2 kbar and the water contents of the melts ranged from nominally dry to approximately 6 wt.% H2O. Accessory phase solubilities are not affected by the water content of the peralkaline melt. By contrast, solubilities are affected by the water content of the subaluminous melt, where the solubilities of all the accessory phases examined increase with the water content of the melt, up to 2 wt.% H2O. At higher water contents, solubilities are nearly constant. It can be concluded that water is not an important control of accessory phase solubility, although the water content will affect diffusivities of components in the melt, thus whether or not accessory phases will be present as restite material. The solubility behaviour in the subaluminous and peralkaline melts supports previous spectroscopic studies, which have observed differences in the coordination of high field strength elements in dry vs. wet subaluminous granitic glasses, but not for peralkaline granitic glasses. Lastly, the fact that wolframite solubility increases with increasing water content in the subaluminous melt suggests that tungsten dissolved as a hexavalent species.  相似文献   
8.
中国大陆科学钻探主孔100~2000米超高压变质岩中的钛矿化   总被引:14,自引:12,他引:14  
中国大陆科学钻探工程100~2000m的岩心、矿心的观察、编录揭示主要有经济价值的舍钛相是金红石.其次是钛磁铁矿。主要含矿岩石是普通金红石榴辉岩和石英金红石榴辉岩,其次有多硅白云母金红石榴辉岩,蓝晶石金红石榴辉岩,金红石黑云绿帘纤闪石岩(退变的石榴辉石岩)和金红石-含钒钛磁铁矿榴辉岩。划分了四个矿化层位。金红石在矿层中的含量一般为2%~5%(体积),多高达8%~10%。金红石的TiO2含量在95%(重量)以上,多产于石英榴辉岩、多硅白云母榴辉岩中。钛磁铁矿的TiO2含量在49%~55%(重量),钛磁铁矿多见于黄铁矿-金红石-钛磁铁矿榴辉岩(546~608m岩性段)中,含钛磁铁矿5%~25%,石榴单辉橄榄岩(608~683m岩性段),含钛磁铁矿达5%~10%和第三含矿层中局部黑云绿帘角闪岩夹层内,舍钛磁铁矿可达6%。30个榴辉岩和超铁镁质岩中8种主要造岩矿物148个点的电子探针分析结果揭示:榴辉岩可分为壳源和幔源两大类,钛磁铁矿富含V、Ni、Cr说明来自幔源,大部分金红石则来自壳源榴辉岩,它们的原岩是曾经居留地表的基性火成岩,在深俯冲的过程中经超高压变质成为含柯石英的榴辉岩。岩石薄片中金红石和柯石英的假像共存于同一石榴石或绿辉石晶粒中,也见金红石粒内有“柯石英”假象,这清楚说明金红石结晶于超高压的峰期变质阶段,在后继的变质地体隆升过程中,钛磁铁矿和金红石都有退变质成为钛铁矿和榍石的种种岩石记录,因此,退变质作用势必导致钛矿品位的降低。  相似文献   
9.
八庙-青山金红石矿床地球化学特征   总被引:6,自引:0,他引:6  
徐少康 《矿产与地质》1999,13(5):293-298
金红石矿床含矿岩石常量元素总体上与玄武岩接近,但以低硅,高钛,高CO2,高碱度为特征。矿床微量元素与地壳的差别显著,稀土元素较高,分布模式呈轻稀土富集型,Eu一般为正常型与碧玄岩最接近,Ti与Ba,Co,Pb,Sr,Th,V,Y及稀土元素呈正相关与Cr和Ni呈负相关,δ^34S多数与(超)铁镁质岩石接近,最大值小于且靠近现代海水。  相似文献   
10.
Trevor H. Green  John Adam 《Lithos》2002,61(3-4):271-282
The solubility of Ti- and P-rich accessory minerals has been examined as a function of pressure and K2O/Na2O ratio in two series of highly evolved silicate systems. These systems correspond to (a) alkaline, varying from alkaline to peralkaline with increasing K2O/Na2O ratio; and (b) strongly metaluminous (essentially trondhjemitic at the lowest K2O/Na2O ratio) and remaining metaluminous with increasing K2O/Na2O ratio (to 3). The experiments were conducted at a fixed temperature of 1000 °C, with water contents varying from 5 wt.% at low pressure (0.5 GPa), increasing through 5–10 wt.% at 1.5–2.5 GPa to 10 wt.% at 3.5 GPa. Pressure was extended outside the normal crustal range, so that the results may also be applied to derivation of hydrous silicic melts from subducted oceanic crust.

For the alkaline composition series, the TiO2 content of the melt at Ti-rich mineral saturation decreases with increasing pressure but is unchanged with increasing K content (at fixed pressure). The P2O5 content of the alkaline melts at apatite saturation increases with increased pressure at 3.5 GPa only, but decreases with increasing K content (and peralkalinity). For the metaluminous composition series (termed as “trondhjemite-based series” (T series)), the TiO2 content of the melt at Ti-rich mineral saturation decreases with increasing pressure and with increasing K content (at fixed pressure). The P2O5 content of the T series melts at apatite saturation is unchanged with increasing pressure, but decreases with increasing K content. The contrasting results for P and Ti saturation levels, as a function of pressure in both compositions, point to contrasting behaviour of Ti and P in the structure of evolved silicate melts. Ti content at Ti-rich mineral saturation is lower in the alkaline compared with the T series at 0.5 GPa, but is similar at higher pressures, whereas P content at apatite saturation is lower in the T series at all pressures studied. The results have application to A-type granite suites that are alkaline to peralkaline, and to I-type metaluminous suites that frequently exhibit differing K2O/Na2O ratios from one suite to another.  相似文献   

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