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111.
This work restored the erosion thickness of the top surface of each Cretaceous formations penetrated by the typical well in the Hari sag, and simulated the subsidence burial history of this well with software BasinMod. It is firstly pointed out that the tectonic subsidence evolution of the Hari sag since the Cretaceous can be divided into four phases: initial subsidence phase, rapid subsidence phase,uplift and erosion phase, and stable slow subsidence phase. A detailed reconstruction of the tectonothermal evolution and hydrocarbon generation histories of typical well was undertaken using the EASY R_0% model, which is constrained by vitrinite reflectance(R_0) and homogenization temperatures of fluid inclusions. In the rapid subsidence phase, the peak period of hydrocarbon generation was reached at c.a.105.59 Ma with the increasing thermal evolution degree. A concomitant rapid increase in paleotemperatures occurred and reached a maximum geothermal gradient of about 43-45℃/km. The main hydrocarbon generation period ensued around 105.59-80.00 Ma and the greatest buried depth of the Hari sag was reached at c.a. 80.00 Ma, when the maximum paleo-temperature was over 180℃.Subsequently, the sag entered an uplift and erosion phase followed by a stable slow subsidence phase during which the temperature gradient, thermal evolution, and hydrocarbon generation decreased gradually. The hydrocarbon accumulation period was discussed based on homogenization temperatures of inclusions and it is believed that two periods of rapid hydrocarbon accumulation events occurred during the Cretaceous rapid subsidence phase. The first accumulation period observed in the Bayingebi Formation(K_1 b) occurred primarily around 105.59-103.50 Ma with temperatures of 125-150℃. The second accumulation period observed in the Suhongtu Formation(K_1 s) occurred primarily around84.00-80.00 Ma with temperatures of 120-130℃. The second is the major accumulation period, and the accumulation mainly occurred in the Late Cretaceous. The hydrocarbon accumulation process was comprehensively controlled by tectono-thermal evolution and hydrocarbon generation history. During the rapid subsidence phase, the paleo temperature and geothermal gradient increased rapidly and resulted in increasing thermal evolution extending into the peak period of hydrocarbon generation,which is the key reason for hydrocarbon filling and accumulation.  相似文献   
112.
柴达木盆地上石炭统克鲁克组是该区重要的古生界勘探层位,组内发育多套良好的碎屑岩层。为探究其岩石物性特征及控制因素,本次以野外露头调查为基础,利用普通薄片、铸体薄片鉴定及扫描电镜等手段,结合物性测试和压汞资料,对克鲁克组碎屑岩纵向分布规律,储层岩性、物性、孔喉特征及孔隙类型进行分析。认为克鲁克地层中克2段发育的三角洲前缘亚相和克3段的具障壁海岸潮坪相的大套含砾粗砂岩、粗砂岩砂体原生、次生孔洞发育,孔喉大、分布集中、分选好,为有利的碎屑岩储层。早成岩期压实作用、重结晶及胶结作用对克鲁克组砂岩的原生孔隙破坏严重,晚成岩期储层改造形成的溶孔、裂缝—溶孔是油气成藏的主要储存空间。该研究为预测柴东石炭系克鲁克组油气有利区域提供依据,为今后该地区的油气勘探提供理论支撑。  相似文献   
113.
糜棱岩韧性变形发生的应变局部化过程,尤其是多相糜棱岩第二相对基质相变形的影响一直是显微构造研究难点.研究表明糜棱岩借助颗粒边界滑移实现多相混合,形成多矿物相集合体.在多相糜棱岩内,第二相在基质相颗粒边界施加齐纳阻力,牵制基质相颗粒边界的迁移速率,破坏基质相颗粒的动态平衡过程,使基质相颗粒位于古应力计对应的颗粒粒度以下,导致基质相整体的表面积增大,促进扩散交换过程,提高了扩散蠕变,降低了基质相位错蠕变和结晶学优选方位(CPO)形成的效率,使变形机制从颗粒粒径不敏感蠕变机制(GSI)过渡为颗粒粒径敏感蠕变机制(GSS).另外,多相糜棱岩内的第二相具有诱导应变局部化的效应,使塑性应变局部化更为强烈,引起物质强度的变化,进而引起岩石变形过程和岩石圈流变行为的改变.选取秦岭群花岗质糜棱岩进行多相矿物糜棱岩定量化研究,结果显示花岗质糜棱岩伴随着云母含量的增多以及各相混合程度的增大,石英的颗粒粒度明显减小,CPO强度显著降低,基质相显微变形受第二相控制逐渐增强.  相似文献   
114.
全风化花岗岩地层稳定性差、遇水易发生崩解,工程上使用常规材料防渗加固注浆时效果较差。针对这一情况,依托湖南省郴州市莽山水库防渗加固灌浆项目,通过自主设计的全风化花岗岩地层注浆室内模拟试验装置,进行模拟注浆试验,实现了浆液在整个注浆过程中的扩散情况模拟,对不同注浆压力、不同位置点所取试样开展单轴抗压、抗剪强度及渗透率测试试验,对不同注浆压力下完整结石体取样观察,研究以全风化花岗岩颗粒为配方主体材料的高固相离析浆液在全风化花岗岩地层的防渗加固效果及浆液扩散模式。结果表明:该浆液在全风化花岗岩地层扩散过程中经历了渗透扩散、挤密压缩、劈裂扩展三个阶段,是一种复合注浆形式;以全风化花岗岩颗粒为主体的高固相离析浆液在全风化花岗岩地层注浆中效果显著,随着注浆压力提升,单轴抗压强度显著提升为原土体的3.25~13.67倍,抗剪强度在不同法向压力情况下提升为原土体的1.63~2.69倍,渗透系数从10?4 cm/s下降至10?5 cm/s甚至10?6 cm/s。  相似文献   
115.
当深海固井遇到天然气水合物地层时,由于水泥浆水化放热,导致水合物的相变平衡条件发生改变,诱发水合物分解,引起二界面胶结质量下降等问题。为提高水合物地层固井质量,可向水泥浆中添加具有吸热控温作用的相变微胶囊,可有效降低固井水泥浆的水化升温。基于此,以配比石蜡为控温芯材、碳酸钙为壁材,利用自组装法制备了一种使用于深水水合物地层固井水泥浆控温微胶囊。由于固井水泥浆在达到水合物地层的过程中,外界温度环境复杂,单一相变温度的控温芯材极易失效。为扩展控温区间,选用切片石蜡与白油作为混合芯材,控温区间达到14.8~39.8 ℃。研究表明,该微胶囊表观形态良好、彼此无团聚,在热循环过程中,不易发生泄漏。与水泥浆复配后,对水泥浆流变性能无明显影响。在低掺加量时,微胶囊主要起降低水泥浆峰值温度的效果,并提升水泥石整体力学强度;高掺加量时,微胶囊既可以有效降低水泥浆峰值温度,也可以明显地延缓水泥浆放热速率。  相似文献   
116.
CINRAD-SA双偏振雷达资料在降水估测中的应用初探   总被引:2,自引:0,他引:2  
陈超  胡志群  胡胜  张扬  李珊珊 《气象》2019,45(1):113-125
对基于水平反射率ZH和差分传播相移率K_(DP)的降水估测综合法R(C)进行了改进,并对广州S波段双偏振雷达2016年2次飑线和2次台风降水过程的Φ_(DP)使用小波分析进行滤波处理,在此基础上使用变距最小二乘法拟合得到K_(DP)的值。分别使用R(C)和R(Z_H)法对2次飑线和2次台风降水过程进行降水估算,将估算结果和雨量计小时雨量进行了对比,并将两种方法的评估结果进行了对比。结果表明:(1)对于飑线类型降水,R(C)法对5 mm·h~(-1)以上的降水估测精度要好于R(Z_H)法,且降水率越大,R(C)法优势越明显,当降水率≥20 mm·h~(-1)时,两次过程R(C)法比R(Z_H)法的平均相对误差(RE)降低了17. 2%,平均绝对误差(AE)减少了1.89 mm,平均均方根误差(RMSE)减少了1.66 mm;(2)对于台风类型降水,R(C)法对5 mm·h~(-1)以上的降水估测精度也好于R(Z_H)法,当降水率≥20 mm·h~(-1)时,两次过程R(C)法比R(Z_H)法的平均RE降低了33. 19%,平均AE减少了3. 95 mm,平均RMSE减少了4.05 mm;(3)对于飑线和台风两种类型降水R(C)法都明显改善了降水率较大时的R(Z_H)法低估问题,但R(C)法在降水率10 mm·h~(-1)时也存在低估,可能是由雨滴谱资料观测误差导致拟合的系数偏小或雷达硬件造成的观测偏差等造成的。  相似文献   
117.
Eclogites from the Kebuerte Valley, Chinese South Tianshan, consist of garnet, omphacite, phengite, paragonite, glaucophane, hornblendic amphibole, epidote, quartz and accessory rutile, titanite, apatite and carbonate minerals with occasional presence of coesite or quartz pseudomorphs after coesite. The eclogites are grouped into two: type I contains porphyroblastic garnet, epidote, paragonite and glaucophane in a matrix dominated by omphacite where the proportion of omphacite and garnet is >50 vol.%; and type II contains porphyroblastic epidote in a matrix consisting mainly of fine‐grained garnet, omphacite and glaucophane where the proportion of omphacite and garnet is <50 vol.%. Garnet in both types of eclogites mostly exhibits core–rim zoning with increasing grossular (Xgr) and pyrope (Xpy) contents, but a few porphyroblastic garnet grains in type I eclogite shows core–mantle zoning with increasing Xpy and a slight decrease in Xgr, and mantle–rim zoning with increases in both Xgr and Xpy. Garnet rims in type I eclogite have higher Xpy than in type II. Petrographic observations and phase equilibria modelling with pseudosections calculated using thermocalc in the NCKMnFMASHO system for three representative samples suggest that the eclogites have experienced four stages of metamorphism: stage I is the pre‐peak temperature prograde heating to the pressure peak (Pmax) which was recognized by the garnet core–mantle zoning with increasing Xpy and decreasing Xgr. The PT conditions at Pmax constrained from garnet mantle or core compositions with minimum Xgr content are 29–30 kbar at 526–540 °C for type I and 28.2 kbar at 518 °C for type II, suggesting an apparent thermal gradient of ~5.5 °C km?1. Stage II is the post‐Pmax decompression and heating to the temperature peak (Tmax), which was modelled from the garnet zoning with increasing Xgr and Xpy contents. The PT conditions at Tmax, defined using the garnet rim compositions with maximum Xpy content and the Si content in phengite, are 24–27 kbar at 590 °C for type I and 22 kbar at 540 °C for type II. Stage III is the post‐Tmax isothermal decompression characterized by the decomposition of lawsonite, which may have resulted in the release of a large amount of fluid bound in the rocks, leading to the formation of epidote, paragonite and glaucophane porphyroblasts. Stage IV is the late retrograde evolution characterized by the overprint of hornblendic amphibole in eclogite and the occurrence of epidote–amphibole facies mineral assemblages in the margins or in the strongly foliated domains of eclogite blocks due to fluid infiltration. The PT estimates obtained from conventional garnet–clinopyroxene–phengite thermobarometry for the Tianshan eclogites are roughly consistent with the P–T conditions of stage II at Tmax, but with large uncertainties in temperature. On the basis of these metamorphic stages or P–T paths, we reinterpreted that the recently reported zircon U–Pb ages for eclogite may date the Tmax stage or the later decompression stage, and the widely distributed (rutile‐bearing) quartz veins in the eclogite terrane may have originated from the lawsonite decomposition during the decompression stage rather than from the transition from blueschist to eclogite as previously proposed.  相似文献   
118.
Monthly sediment load and streamflow series spanning 1963–2004 from four hydrological stations situation in the main stem of the Yangtze River, China, are analysed using scanning t‐test and the simple two‐phase linear regression scheme. Results indicate significant changes in the sediment load and streamflow from the upper reach to the lower reach of the Yangtze River. Relatively consistent positive coherency relations can be detected between streamflow and sediment load in the upper reach and negative coherency in the middle and lower reaches. Interestingly, negative coherency is found mainly for larger time scales. Changes in sediment load are the result mainly of human influence; specifically, the construction of water reservoirs may be the major cause of negative coherency. Accentuating the human influence from the upper to the lower reach results in inconsistent correlations between sediment load and streamflow. Decreasing sediment load being observed in recent years has the potential to alter the topographical properties of the river channel and the consequent development and recession of the Yangtze Delta. Results of this study are of practical significance for river channel management and evaluation of the influence of human activities on the hydrological regimes of large rivers. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   
119.
Experimental study on metallation of tetrapyrroles in biphasic systems showed that complexation with metal cations of the first transition series is a feasible under chemical environments similar to the naturally occurring ones. The metal transport from the aqueous media to the organic, which is a novel approach using naturally occurring fatty acids hydroxy aromatic compounds and thiols, is demonstrated. Selectivity between Ni2+ and VO2+ complexation is achieved under sulfurous rich conditions. The kinetic implications are discussed in view of their geoenvironmental applicability.  相似文献   
120.
对Li_2O-(Mg、Zn、Ni)O-V_2O_5三元体系在500—800℃相图的研究表明,在每个系统内部都出现了一个依端员组分摩尔比为1:2:1的化合物。即橄榄石型的LiMgVO_4,硅铍石型的LiZnVO_4和尖晶石型的LiNiVO_4。不同的是,Li_2O-MgO-V_2O_5中发现了第二个三元相和一个固溶体。LiO_2-NiO-V_2O_6中得出一个固溶体,而LiZnNO_4中未得固溶体。  相似文献   
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