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81.
《International Geology Review》2012,54(18):2249-2275
ABSTRACT

The Piqiang intrusion is one of the two important ma?c-ultrama?c layered intrusions that host giant Fe-Ti-V oxide deposits in the Permian Tarim Large Igneous Province, NW China. The intrusion mainly consists of gabbro, anorthosite and minor plagioclase-bearing clinopyroxenite in the marginal zone. Disseminated to massive Fe-Ti oxide ores occur as layers and lenses within the gabbro. SHRIMP zircon U-Pb results from both a gabbro from the Piqiang intrusion and a granite from the surrounding granitic dyke yield ages of ~270 Ma. Geochemically, the Piqiang silicate rocks are enriched in light rare earth elements (LREE) and large ion lithophile elements (LILE), moderately depleted in high ?eld strength elements (HFSE), and have a limited range of Sr-Nd-Hf isotopic compositions. The similar mineralogy, mineral compositions, and trace element characteristics of the layered units suggest that all the rocks are co-magmatic. The parental magma is Fe-Ti-rich and is akin to the most primitive diabasic dyke which is associated with the Piqiang intrusion. Partial melting of the Tarim mantle plume with involvement of a subduction-metasomatized lithospheric mantle source best explains the geochemistry and petrogenesis of the parental magmas of the Piqiang intrusion. We propose that the lithospheric mantle source may have been metasomatized by subduction-related materials and the metasomatic enrichment of this source region which may be correlated with oceanic sediment recycling during southward subduction of the South Tianshan oceanic slab during the Early-Middle Paleozoic. Crystal settling and mechanical sorting is the predominant process responsible for the formation of the massive Fe-Ti oxide ores in the Piqiang intrusion. Central to ore formation is a combination of the protracted differentiation history of a Fe-Ti-enriched parental magma and the later addition of external H2O from the country rocks to the slowly cooling magma chamber.  相似文献   
82.
为了考察铁锰氧化物对酚类污染物的氧化降解能力,采用天然以及合成的铁锰氧化物对苯酚的氧化降解进行对比实验研究。土壤中铁锰氧化物样品分别为天然针铁矿及氧化锰,合成铁锰氧化物样品分别为合成针铁矿及软锰矿。结果表明:苯酚与铁锰氧化物发生氧化还原作用时,还可能与土壤中杂质发生吸附等作用;铁锰氧化物还原反应强度随着反应介质pH值的升高而迅速下降;可用零级反应动力学方程拟合铁氧化物还原溶解反应,针铁矿溶解反应的强度与介质的pH值呈负相关关系;天然针铁矿对酚类污染物的氧化降解能力明显高于合成针铁矿,pH值对天然针铁矿溶解反应影响较大;可用一级指数衰减方程拟合锰氧化物还原溶解反应,锰氧化物溶解反应的强度与介质的pH值呈指数衰减关系;pH值对软锰矿还原溶解反应的影响大于对土壤中氧化锰的影响,pH值越小,影响越显著;对比pH值对铁和锰还原作用的影响发现,在pH=6.5时,锰氧化物仍有较强的氧化性能。  相似文献   
83.
铁锰氧化物对苯酚氧化降解的实验研究   总被引:1,自引:0,他引:1  
为了考察铁锰氧化物对酚类污染物的氧化降解能力,采用天然以及合成的铁锰氧化物对苯酚的氧化降解进行对比实验研究.土壤中铁锰氧化物样品分别为天然针铁矿及氧化锰,合成铁锰氧化物样品分别为合成针铁矿及软锰矿.结果表明:苯酚与铁锰氧化物发生氧化还原作用时,还可能与土壤中杂质发生吸附等作用;铁锰氧化物还原反应强度随着反应介质pH值的...  相似文献   
84.
用WB和JC标准水合法测定轻烧MgO粉的活性MgO含量,对测定结果进行方差和误差分析,并研究了水化时间对测定结果的影响。结果表明,两种方法存在显著性差异,WB和JC水合法的平均相对误差分别为1.31%和-19.85%,WB水合法精密度远高于JC水合法。以WB水合法为基准,JC水合法的平均相对误差大于-20%,远远超过行业标准中规定的±3%。因此,对于镁水泥原料MgO中活性含量的定量分析,不能采用JC方法,必须采用WB方法。此外,发现水化3 h已经接近活性氧化镁的水化平衡,为修订WB标准方法提供了参考依据。  相似文献   
85.
氧化亚氮(N2O)是大气中重要和微量的温室气体,且在平流层N2O形成NO自由基与O3发生反应破坏臭氧层.海洋是大气中N2O净源,但由于海洋中生物化学过程的复杂性,有关N2O形成机制至今是人们研究的重点和难点.应用稳定同位素分馏原理对海洋中N2O形成机制的研究,区分海洋中通过硝化和反硝化过程不同途径产生的N2O过程,为深入研究海洋中N2O循环、估算将来大气中N2O浓度变化提供有用工具.  相似文献   
86.
以铸态Ni-Cr-Fe合金为试样,于1 050℃湿氢气氛下恒温氧化20 h。通过氧化增重、SEM/EDS以及薄膜X-射线衍射等方法研究了氧分压对该合金在弱氧化性气氛下氧化成膜特性的影响。结果表明:表面氧化膜从外到内氧化物组成依次为:MnCr2O4、Cr2O3以及SiO2。氧化膜的厚度、组成及形貌与体系的氧分压密切相关,中等氧分压(15.9×10-18atm)有利于表面尖晶石的形成;较低氧分压有利于形成厚而多孔的氧化膜,而高氧分压则趋向于形成薄而致密的氧化膜。  相似文献   
87.
In the Segura area, Variscan S-type granites, aplite veins and lepidolite-subtype granitic aplite-pegmatite veins intruded the Cambrian schist-metagraywacke complex. The granites are syn D3. Aplite veins also intruded the granites. Two-mica granite and muscovite granite have similar ages of 311.0 ± 0.5 Ma and 312.9 ± 2.0 Ma but are not genetically related, as indicated by their geochemical characteristics and (87Sr/86Sr)311 values. They correspond to distinct pulses of magma derived by partial melting of heterogeneous metapelitic rocks. Major and trace elements suggest fractionation trends for: (a) muscovite granite and aplite veins; (b) two-mica granite and lepidolite-subtype aplite-pegmatite veins, but with a gap in most of these trends. Least square analysis for major elements, and modeling of trace elements, indicate that the aplite veins were derived from the muscovite granite magma by fractional crystallization of quartz, plagioclase, K-feldspar and ilmenite. This is supported by the similar (87Sr/86Sr)311 and δ18O values and the behavior of P2O5 in K-feldspar and albite. The decrease in (87Sr/86Sr)311 and strong increase (1.6‰) in δ18O from two-mica granite to lepidolite-subtype aplite-pegmatite veins, and the behaviors of Ca, Mn and F of hydroxylapatite indicate that these veins are not related to the two-mica granite.  相似文献   
88.
http://www.sciencedirect.com/science/article/pii/S1674987113000595   总被引:11,自引:0,他引:11  
Magmatic oxide deposits in the~260 Ma Emeishan Large Igneous Province(ELIP),SW China and northern Vietnam,are important sources of Fe,Ti and V.Some giant magmatic Fe-Ti-V oxide deposits, such as the Panzhihua,Hongge,and Baima deposits,are well described in the literature and are hosted in layered mafic-ultramafic intrusions in the Panxi region,the central ELIP.The same type of ELIP- related deposits also occur far to the south and include the Anyi deposit,about 130 km south of Panzhihua,and the Mianhuadi deposit in the Red River fault zone.The Anyi deposit is relatively small but is similarly hosted in a layered mafic intrusion.The Mianhuadi deposit has a zircon U-Pb age of~260 Ma and is thus contemporaneous with the ELIP.This deposit was variably metamorphosed during the Indosinian orogeny and Red River faulting.Compositionally,magnetite of the Mianhuadi deposit contains smaller amounts of Ti and V than that of the other deposits,possibly attributable to the later metamorphism.The distribution of the oxide ore deposits is not related to the domal structure of the ELIP.One major feature of all the oxide deposits in the ELIP is the spatial association of oxide-bearing gabbroic intrusions,syenitic plutons and high-Ti flood basalts.Thus,we propose that magmas from a mantle plume were emplaced into a shallow magma chamber where they were evolved into a field of liquid immiscibility to form two silicate liquids,one with an extremely Fe-Ti-rich gabbroic composition and the other syenitic.An immiscible Fe-Ti-(P) oxide melt may then separate from the mafic magmas to form oxide deposits.The parental magmas from which these deposits formed were likely Fe-Ti-rich picritic in composition and were derived from enriched asthenospheric mantle at a greater depth than the magmas that produced sulfide-bearing intrusions of the ELIP.  相似文献   
89.
Recent work on the Panzhihua intrusion has produced two separate models for the crystallisation of the intrusion:(1) low-Ti,high CaO and low H2O(0.5 wt.%) parent magma(equivalent to Emeishan low-Ti basalt) at FMQ;and(2) high-Ti,low CaO and higher H2O(>1.5 wt.%) parent magma(equivalent to Emeishan high-Ti basalt) at FMQ + 1.5.Modelling of these parent magma compositions produces significantly different results. We present here detailed f(O2) and H2O modelling for average compositions of both Emeishan high-Ti and low-Ti ferrobasalts in order to constrain the effects on crystallisation sequences for Emeishan ultra-mafic -mafic layered intrusions.Modelling is consistent with numerous experimental studies on ferro-basaltic magmas from other localities(e.g.Skaergaard intrusion).Modelling is compared with the geology of the Panzhihua intrusion in order to constrain the crystallisation of the gabbroic rocks and the Fe-Ti oxides ore layers.We suggest that the gabbroic rocks at the Panzhihua intrusion can be best explained by crystallisation from a parent magma similar to that of the high-Ti Emeishan basalt at moderate H2O contents(0.5-1 wt.%) but at the lower end of TiO2 content for typical high-Ti basalts(2.5 wt.%TiO2). Distinct silicate disequilibrium textures in the Fe-Ti oxide ore layers suggest that an influx of H2O may be responsible for changing the crystallisation path.An increase in H2O during crystallisation of gabbroic rocks will result in the depression of silicate liquidus temperatures and resultant disequilibrium with the liquid.Continued cooling of the magma with high H2O then results in precipitation of Mt-Uv alone. The H2O content of parent magmas for mafic layered intrusions associated with the ELIP is an important variable.H2O alters the crystallisation sequence of the basaltic magmas so that at high H2O and f(O2) Mt -Uv crystallises earlier than plagioclase and clinopyroxene.Furthermore,the addition of H2O to an anhydrous magma can explain silicate disequilibrium texture observed in the Fe-Ti oxide ore layers.  相似文献   
90.
东天山香山铜镍-钛铁成矿与两类岩浆演化关系探讨   总被引:1,自引:0,他引:1  
香山矿床是东天山唯一一个铜镍矿体与钛铁矿体共存的复合型矿床,目前普遍被认为是同源岩浆高度演化的产物。但为何区内众多同时代镁铁-超镁铁质岩体中只有香山岩体产出有大型钛铁矿床?这一问题仍有待进一步探讨。本文通过系统对比香山与其相邻的黄山东、黄山和黄山南等典型铜镍矿的地球化学特征、母岩浆性质及岩浆演化过程,认为香山岩体母岩浆相对其相邻典型铜镍矿床并不富集Fe和Ti,且其母岩浆早期演化过程及分异演化程度相似。模拟计算表明:岩浆体系早期都处于较还原的环境(f_(O_2)QFM+1),而且都发生了大量橄榄石、斜方辉石和单斜辉石的分离结晶和硫化物的熔离,由此消耗了岩浆体系中大量的Fe,导致残余岩浆中Fe含量降低;另外在岩浆演化的各阶段,尤其到岩浆演化后期,大量角闪石的结晶进一步降低了残余岩浆中的Fe和Ti的含量,不能造成Fe和Ti的逐渐富集,据此我们认为同源岩浆演化不具备形成钛铁矿床的物质基础。通过初步对比东天山地区典型铜镍矿床和钛铁矿床与该地区早二叠世两类玄武岩的地球化学特征及演化趋势,我们初步推测东天山地区铜镍成矿与钛铁成矿是两类不同性质岩浆独立演化的产物,铜镍成矿可能与拉斑玄武质岩浆演化密切相关,而钛铁矿则可能与碱性玄武岩演化密切相关。  相似文献   
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