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71.
新型电致冷半导体探测器的应用   总被引:1,自引:0,他引:1  
吕军  侯新生 《物探与化探》2006,30(4):374-376
用于探测X射线的锂漂移型硅探测器需在液氮条件下低温保存和使用,因此限制了其应用范围。介绍了一种采用电致冷方式的新型半导体探测器,并通过把液氮致冷的Si(Li)探测器与电致冷的Si-PIN探测器进行比较,论证了电致冷方法的可行性。  相似文献   
72.
Studies of modern cyanobacterial mats and biofilms show that they can precipitate minerals as a consequence of metabolic and degradational activities paired with ambient hydrochemical conditions. This study looked at modern microbial mats forming giant, tower‐like, groundwater‐fed, calcareous microbialites in the world's largest, highly alkaline lake; Van Gölü (Lake Van), East Turkey. Results show that microbial systems play a role not only in carbonate precipitation but also in the formation of siliceous mineral phases. Transmitted light microscopy, scanning electron microscopy and spectral observations revealed that, within the extracellular polymeric substances excreted by the mats abundant minute aragonite grains precipitated first in vivo. These minute grains were quickly succeeded and/or supplemented in the dead biomass of the cyanobacterial mat by authigenic Al–Mg–Fe siliceous phases. Silicon dioxide is available in large concentrations in the highly alkaline water of Lake Van. Divalent cations (Ca and Mg) are delivered to the microbialites mostly by groundwater springs. The precipitation of the fine‐grained siliceous phases is probably mediated by bacteria degrading the cyanobacterial biomass and complexing the excessive cations with their extracellular polymeric envelopes. The bacteria serve as nucleation centres for the subsequent precipitation of siliceous mineral phases. Generally, the biphasic (calcareous and siliceous) mineralization – characterizing Lake Van microbialites – is controlled by their interior highly dynamic hydrogeochemical situation. There, the dramatically different alkaline lake water and the Ca–Mg‐charged groundwater mix at various rates. The early diagenetic replacement of the in vivo aragonite by authigenic siliceous phases significantly increases the fossilization potential of the mat‐forming cyanobacteria. Lake Van and its giant microbialite tufa towers act as a model explaining the transformation of early diagenetic mineral phases observed in many modern and ancient carbonate marine deposits, particularly those influenced by diffusion of silica‐enriched and metal‐enriched pore waters from below the water–sediment interface.  相似文献   
73.
康欢  李大鹏  陈岳龙  鲁震 《现代地质》2016,30(5):1026-1037
对保山地块东缘高Si花岗岩开展矿物化学、岩石地球化学及锆石U Pb Hf系统研究,结果表明该高Si花岗岩为具钙碱性、强过铝质特征的S型花岗岩。锆石U Pb同位素分析表明,高Si花岗岩侵位于454 Ma,并含有800~1 100 Ma的继承锆石。锆石Hf同位素分析表明其岩浆锆石具有与青藏高原及东南缘同时代长英质侵入体相似的Hf同位素组成,暗示其相似的岩浆起源。矿物化学、同位素组成及Melts模拟计算结果表明,保山东缘高Si花岗岩为一系列复杂作用的结果:高硅花岗岩母岩浆起源于该区沉积岩部分熔融;熔体形成后经高度分异演化,在侵位过程中同化混染围岩;岩浆冷凝至固相线下部分矿物再平衡。保山东缘高Si花岗岩体与平河花岗岩体具相似年龄和地球化学特征,暗示它们之间可能存在类似的成因机制。  相似文献   
74.
拉萨地块南木林盆地林子宗群火山机构内发育有斯弄多隐爆角砾岩型、热液脉型Ag-Pb-Zn矿床,该矿床金属矿物为闪锌矿、方铅矿,少量黄铜矿和辉银矿,蚀变矿物为绢云母、伊利石、玉髓、蒙脱石、碧玉、方解石、菱锰矿和菱铁矿,符合低硫型浅成低温热液矿床的基本特征。本次研究对陆相火山岩中热泉喷口的硅质条带及穿切矿体石英脉进行了Si、H、O同位素测试,结果表明:(1)硅质条带的石英单矿物δ~(30)Si_(NBS-28)为-1.2‰~-0.4‰,记录有热水沉积Si同位素地球化学特征,为古热泉硅华成因;(2)受后期火山热液作用改造的热水沉积硅质条带全岩δ~(30)Si_(NBS-28)为-0.2‰~+0.3‰,显示火山岩与热水沉积岩混合特征;(3)穿切矿体石英脉δ~(30) Si_(NBS-28)值为-0.8‰~-0.1‰,与热水沉积硅质条带石英单矿物Si同位素组成一致,显示低温成因高Δ30Si同位素分馏值特征;(4)石英脉和硅质条带全岩的流体包裹体氢氧同位素特征显示大气水与火山岩发生了水-岩交换作用的"氧同位素漂移"现象,说明成矿流体在火山岩地层中经历了长期的循环作用。因此,Si-H-O稳定同位素指示:矿区内仍保留有古热泉喷口,表明矿区自古新世火山岩喷发和成矿后,剥蚀程度低,"缺位"寻找低硫化浅成低温热液型Au-Ag矿床的勘查潜力较大,低δ~(30)Si_(NBS-28)值石英脉和硅化是重要找矿标志。  相似文献   
75.
河北山前平原地下水^32Si年龄初探   总被引:6,自引:3,他引:3  
^32Si是放射性同位素,半衰期约140a可以测定50~1000a地下水的年龄,本文用Fe(OH)3共沉淀法从天然水中提取SiO2回收率可达30%~98%,然后提取和纯化^32P,将H3PO4溶液和Pico-flour^TMLLT混合制备计数溶液,用液体闪烁计数法测量中^32P的放射性,本底计数为4.80cph,仪器效率为45.34%,然后用公式计算样品的^32Si放射性浓度和地下水的^32Si年  相似文献   
76.
硅藻土的29Si魔角旋转核磁共振谱研究   总被引:2,自引:1,他引:1  
对广东,浙江,云南等不同矿床硅藻土的^29SiMASNMR谱进行了讨论,谱上出现了个不同化学位移及不同强度的信号,分别为-110.1*10^-6---112.1*10^-6,-91.1*10^-6--91.6*10^-6,-106.2*10^-6--107.1*10^-6,-100*10^-6--102.5*10^-6。这些信号分别属于硅藻硅质,高龄石和石英的^29Si共振。硅藻的硅质骨架与蛋白石  相似文献   
77.
Due to the major role played by diatoms in the biological pump of CO2, and to the presence of silica-rich sediments in areas that play a major role in air–sea CO2 exchange (e.g. the Southern Ocean and the Equatorial Pacific), opal has a strong potential as a proxy for paleoproductivity reconstructions. However, because of spatial variations in the biogenic silica preservation, and in the degree of coupling between the marine Si and C biogeochemical cycles, paleoreconstructions are not straitghtforward. A better calibration of this proxy in the modern ocean is required, which needs a good understanding of the mechanisms that control the Si cycle, in close relation to the carbon cycle.This review of the Si cycle in the modern ocean starts with the mechanisms that control the uptake of silicic acid (Si(OH)4) by diatoms and the subsequent silicification processes, the regulatory mechanisms of which are uncoupled. This has strong implications for the direct measurement in the field of the kinetics of Si(OH)4 uptake and diatom growth. It also strongly influences the Si:C ratio within diatoms, clearly linked to environmental conditions. Diatoms tend to dominate new production at marine ergoclines. At depth, they also succeed to form mats, which sedimentation is at the origin of laminated sediments and marine sapropels. The concentration of Si(OH)4 with respect to other macronutrients exerts a major influence on diatom dominance and on the rain ratio between siliceous and calcareous material, which severely impacts surface waters pCO2. A compilation of biogenic fluxes collected at about 40 sites by means of sediment traps also shows a remarkable pattern of increasing BSi:Corg ratio along the path of the “conveyor belt”, accompanying the relative enrichment of waters in Si compared to N and P. This observation suggests an extension of the Si pump model described by Dugdale and Wilkerson (Dugdale, R.C., Wilkerson, F.P., 1998. Understanding the eastern equatorial Pacific as a continuous new production system regulating on silicate. Nature 391, 270–273.), giving to Si(OH)4 a major role in the control of the rain ratio, which is of major importance in the global carbon cycle.The fate of the BSi produced in surface waters is then described, in relation to Corg, in terms of both dissolution and preservation mechanisms. Difficulties in quantifying the dissolution of biogenic silica in the water column as well as the sinking rates and forms of BSi to the deep, provide evidence for a major gap in our understanding of the mechanisms controlling the competition between retention in and export from surface waters. The relative influences of environmental conditions, seasonality, food web structure or aggregation are however explored. Quantitatively, assuming steady state, the measurements of the opal rain rate by means of sediment traps matches reasonably well those obtained by adding the recycling and burial fluxes in the underlying abyssal sediments, for most of the sites where such a comparison is possible. The major exception is the Southern Ocean where sediment focusing precludes the closing of mass balances. Focusing in fact is also an important aspect of the downward revision of the importance of Southern Ocean sediments in the global biogenic silica accumulation. Qualitatively, little is known about the duration of the transfer through the deep and the quality of the material that reaches the seabed, which is suggested to represent a major gap in our understanding of the processes governing the early diagenesis of BSi in sediments. The sediment composition (special emphasis on Al availability), the sedimentation rate or bioturbation are shown to exert an important control on the competition between dissolution and preservation of BSi in sediments. It is suggested that a primary control on the kinetic and thermodynamic properties of BSi dissolution, both in coastal and abyssal sediments, is exerted by water column processes, either occuring in surface waters during the formation of the frustules, or linked to the transfer of the particles through the water column, which duration may influence the quality of the biogenic rain. This highlights the importance of studying the factors controlling the degree of coupling between pelagic and benthic processes in various regions of the world ocean, and its consequences, not only in terms of benthic biology but also for the constitution of the sediment archive.The last section, first calls for the end of the “NPZD” models, and for the introduction of processes linked to the Si cycle, into models describing the phytoplankton cycles in surface waters and the early diagenesis of BSi in sediments. It also calls for the creation of an integrated 1-D diagnostic model of the Si:C coupling, for a better understanding of the interactions between surface waters, deep waters and the upper sedimentary column. The importance of Si(OH)4 in the control of the rain ratio and the improved parametrization of the Si cycle in the 1-D diagnostic models should lead to a reasonable incorporation of the Si cycle into 3-D regional circulation models and OGCMs, with important implications for climate change studies and paleoreconstructions at regional and global scale.  相似文献   
78.
2017年6月在珠江口及近岸海域61个站位采集了悬浮颗粒物生物硅(BSi,biogenic silica)和叶绿素a(Chl a)。利用RAGUENEAU et al(2005)提出的碱提取法测定了悬浮颗粒物生物硅,探讨不同环境条件下BSi浓度以及碱性提取液中岩源硅(LSi,lithogenic silica)的干扰程度。结果显示,Chl a质量浓度范围为0.06~8.64 μg·L-1,悬浮颗粒物BSi浓度从低于检测限到14.3 μmol·L-1,LSi浓度范围为0.00~9.56 μmol·L-1;LSi/(LSi+BSi)比均值为0.38 mol·mol-1。提取液中测得的Si/Al比均值为2.42 mol·mol-1,与RAGUENEAU et al(2005)报道值接近。研究区域内的表层BSi反映了硅藻的生物量,与Chl a存在显著线性相关。LSi对BSi测量的干扰程度存在明显的空间差异,总体上近岸BSi和LSi高,LSi/(LSi+BSi)比低;外海BSi和LSi低,LSi/(LSi+BSi)比高;河口内BSi低,LSi高,LSi/(LSi+BSi)比高;上升流区BSi和LSi高,LSi/(LSi+BSi)比高;底层较表层具有更高的LSi和LSi/(LSi+BSi)比。最后,对常用的几种碱提取法在应用时存在的问题作了探讨。  相似文献   
79.
[研究目的]西秦岭凤太矿集区是秦岭铅锌金多金属成矿带重要组成部分,但对矿集区铅锌矿的矿床类型和控矿因素一直存在争议.[研究方法]通过对凤太矿集区内具有代表性的铅硐山铅锌矿进行详细的野外调查和资料梳理,论述了该矿床的硅钙面控矿特征.[研究结果]认为作为凤太盆地铅锌矿底板的古道岭组灰岩,为偏碱性的Ca质岩石,顶板星红铺组千...  相似文献   
80.
Character of the Si and Al Phases in Coal Gangue and Its Ash   总被引:1,自引:0,他引:1  
Abstract: Analysis of the Si and Al phases in coal gangue fuel and its ash is important for use of coal gangue ashes. A comprehensive study by theoretical and experimental analyses with differential thermal analysis, X-ray diffraction and Infrared Spectroscopy has been made in the present article to explore the diagram of the Si and Al phases in coal gangue fuel and its ashes. It is found that kaolinite and quartz are the main phases in coal gangue fuel. The ratio of moles Al2O3 to SiO2 (i.e., Al2O3 (mole) /SiO2 (mole)) is usually no more than 0.5 in most coal gangue fuel and its ashes. The kaolinit at about 984°C releases a large quantity of SiO2, which makes calcine coal gangue more active than coal gangue itself. The relationship between the ratio Al2O3 (mole)/SiO2(mole) and the components of coal gangue ash is analyzed, resulting in a formula to calculate the quantity of each phase. Applying the formula to the testing samples from an electric plant in north China supports the above conclusions.  相似文献   
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