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1.
晋西北地区表层土壤粒度与地球化学元素组成   总被引:1,自引:1,他引:0  
对晋西北地区表层土壤的物质组成进行研究,可以明确其物质来源、沉积环境及化学风化特征。选择区内表层土壤(深度0、10、20 cm)及其附近的河流沉积物,进行粒度和化学元素组成测试。结果表明:(1)晋西北地区表层土壤粒度组成以黏土和粉沙为主,且有自地表向下粗颗粒组分含量增加的趋势。(2)常量化学元素组成以SiO2、Al2O3、CaO、Fe2O3为主,其余元素含量均较低。化学元素组成模式表明研究区内表层土壤物质与黄土高原腹地黄土有相同的物质源区,黄河河流沉积物对其贡献不大。(3)晋西北表层土壤的CIA值为52.70~57.89,平均54.06,说明它们的化学风化程度较低,处于早期的脱Na、Ca阶段。这是由于研究区地理位置比洛川更靠北,气温和降水量均低于洛川,降水量与兰州相差不大,但是年平均气温和年温差比兰州低。该研究明确了晋西北地区表层土壤的物质组成特征,为区域潜在沙漠化危害防治提供了数据支撑。  相似文献   
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The soil factor is crucial in controlling and properly modeling the initiation and development of ephemeral gullies (EGs). Usually, EG initiation has been related to various soil properties (i.e. sealing, critical shear stress, moisture, texture, etc.); meanwhile, the total growth of each EG (erosion rate) has been linked with proper soil erodibility. But, despite the studies to determine the influence of soil erodibility on (ephemeral) gully erosion, a universal approach is still lacking. This is due to the complex relationship and interactions between soil properties and the erosive process. A feasible soil characterization of EG erosion prediction on a large scale should be based on simple, quick and inexpensive tests to perform. The objective of this study was to identify and assess the soil properties – easily and quickly to determine – which best reflect soil erodibility on EG erosion. Forty‐nine different physical–chemical soil properties that may participate in establishing soil erodibility were determined on agricultural soils affected by the formation of EGs in Spain and Italy. Experiments were conducted in the laboratory and in the field (in the vicinity of the erosion paths). Because of its importance in controlling EG erosion, five variables related to antecedent moisture prior to the event that generated the gullies and two properties related to landscape topography were obtained for each situation. The most relevant variables were detected using multivariate analysis. The results defined 13 key variables: water content before the initiation of EGs, organic matter content, cation exchange capacity, relative sealing index, two granulometric and organic matter indices, seal permeability, aggregates stability (three index), crust penetration resistance, shear strength and an erodibility index obtained from the Jet Test erosion apparatus. The latter is proposed as a useful technique to evaluate and predict soil loss caused by EG erosion. Copyright © 2018 John Wiley & Sons, Ltd.  相似文献   
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本文以全国化工产业密集区——长三角地区为例,基于规模以上中国工业企业详细数据,从化工企业入园率的视角出发,综合运用均值中心、标准差椭圆、核密度分析及空间自相关等分析方法,分析并揭示了1998—2013年长三角地区化工产业时空格局演化规律及影响因素。研究结果表明:1998—2013年长三角地区化工企业总体上呈现不断增长趋势,入园率由6.19%提升到36.98%;化工企业“西北-东南”方向分布明显,且近似呈“先东南,后西北”的路径迁移规律,较之全部企业,入园企业具有更高的离散度、更大的迁移幅度,入园企业与全部企业逐步由空间失配演变为空间匹配;中心集聚与外围扩散态势并存,发育并逐渐形成了环太湖集聚区、沿杭州湾集聚区、沿长江密集带及沿海密集带四大化工产业集聚片区,化工产业的区域空间结构趋于复杂化、有序化与稳定化;地级尺度上化工企业入园率不断提升,2003年与2013年呈显著的空间正相关,热点区逐渐由浙江东南转移到苏皖北部,冷点区从安徽北部迁移到浙江西北,基本完成了空间格局上的对称反转变换,但化工企业入园率与空间密度分布一直处于错配失衡状态。通过结合化工产业特性与长三角区域特征,定性探讨了长三角地区化工产业时空格局演化的影响因素,特别是阐述了化工产业“园区化”进程的作用机制。  相似文献   
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钟翼  许建新  韩积斌  徐凯 《盐湖研究》2020,28(1):112-122
为了解阿拉尔河悬浮物对铀的吸附特性,通过静态吸附实验,研究了吸附时间、pH值、温度和铀初始浓度等因素对模拟含铀水中U(VI)去除率的影响,并从热力学和动力学方面对吸附过程进行了分析。结果表明,在T=25℃,溶液初始pH=7,接触时间为16 h时,悬浮物对铀的平衡吸附率最佳,为95.48%。随着铀初始浓度的增加,吸附量增加,但吸附率随之下降,升高温度有利于铀的吸附。铀在悬浮物上的吸附过程符合Langmuir等温吸附方程,说明悬浮物对铀为单分子层吸附,且化学吸附占主导地位。吸附动力学过程可用准二级吸附动力学模型描述,表明吸附主要受动力学控制,由两个以上步骤共同控制。FTIR和EDS分析结果表明,吸附过程中铀主要与悬浮物表面活性基团螯合并以表面络合吸附为主。吸附前后的能谱对比分析表明,吸附过程中存在离子交换行为。因此,悬浮物对铀的吸附机理是以表面络合吸附和离子交换为主、物理吸附为辅的混合吸附过程。  相似文献   
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The size distributions of sediment delivered from hillslopes to rivers profoundly influence river morphodynamics, including river incision into bedrock and the quality of aquatic habitat. Yet little is known about the factors that influence size distributions of sediment produced by weathering on hillslopes. We present results of a field study of hillslope sediment size distributions at Inyo Creek, a steep catchment in granitic bedrock of the Sierra Nevada, USA. Particles sampled near the base of hillslopes, adjacent to the trunk stream, show a pronounced decrease in sediment size with decreasing sample elevation across all but the coarsest size classes. Measured size distributions become increasingly bimodal with decreasing elevation, exhibiting a coarse, bouldery mode that does not change with elevation and a more abundant finer mode that shifts from cobbles at the highest elevations to gravel at mid elevations and finally to sand at low elevations. We interpret these altitudinal variations in hillslope sediment size to reflect changes in physical, chemical, and biological weathering that can be explained by the catchment's strong altitudinal gradients in topography, climate, and vegetation cover. Because elevation and travel distance to the outlet are closely coupled, the altitudinal trends in sediment size produce a systematic decrease in sediment size along hillslopes parallel to the trunk stream. We refer to this phenomenon as ‘downvalley fining.’ Forward modeling shows that downvalley fining of hillslope sediment is necessary for downstream fining of the long-term average flux of coarse sediment in mountain landscapes where hillslopes and channels are coupled and long-term net sediment deposition is negligible. The model also shows that abrasion plays a secondary role in downstream fining of coarse sediment flux but plays a dominant role in partitioning between the bedload and suspended load. Patterns observed at Inyo Creek may be widespread in mountain ranges around the world. © 2020 The Authors. Earth Surface Processes and Landforms published by John Wiley & Sons Ltd.  相似文献   
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Rhenium–osmium geochronometry for samples with low Re and complex matrices requires improved Re extraction methods. Here, we investigate plausible controls on efficiency and efficacy of Re extraction during our anion resin bead purification. Four different protocols are compared, each isolating a single variable to test. Rhenium concentrations for solutions at each step of each protocol document differences in chemical recovery/yield. The negative‐thermal ionisation mass spectrometry (N‐TIMS) signal intensity serves as a proxy for Re yield and purity. These data document correlations between the N‐TIMS signal intensity and (a) the duration of anion resin bead conditioning prior to loading with Re‐bearing solution, and (b) both duration and strength of nitric acid used during rinsing of the Re‐loaded anion resin bead. The optimal protocol improved Re signal intensity around fourteen times compared with our current Re extraction protocol, an aggregate of 2.4 times improvement in chemical recovery (yield) and 5.8 times improvement in emission efficiency (purity). Repeated N‐TIMS isotopic measurements on our in‐house Re standard solution (1407) verify that our optimal protocol‐3 does not fractionate Re isotopes. The improved anion resin bead method considerably lowers the Re detection limit and allows Re‐Os isotopic analysis of picogram‐level Re hosted in geological samples with complex matrices.  相似文献   
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增强型地热系统(EGS)用于通过人工形成地热储层的方法从深部低渗透性岩体中开采地热能;国际上常采用水力压裂辅以化学刺激的方法改造EGS 储层以提高其渗透率。本文以采自青海共和盆地的花岗闪长岩样品为对象,选用3种不同化学刺激剂(氢氧化钠、盐酸和土酸),在3组不同注入流速条件下开展了系统化学刺激实验。结果表明:注入盐酸和土酸后样品渗透率均有提高,且采用土酸时渗透率提高幅度明显大于盐酸;但注入氢氧化钠后,样品渗透率反而降低。在3类化学刺激剂中,土酸对长石类矿物的溶蚀能力最强,而氢氧化钠溶液对石英的溶蚀能力最强,但氢氧化钠溶液在溶解岩石样品裂隙表面矿物后极易形成非定形态二氧化硅或非定形态铝硅酸盐蚀变矿物并阻塞裂隙,反而对化学刺激效果造成负面影响。总体来看,土酸是青海共和盆地干热岩体的最佳化学刺激剂。在中等注入速度(3 mL·min-1)条件下,土酸对岩石样品的溶蚀程度就可达到最高;在此基础上进一步降低流速,则可能使溶解组分更易从液相中沉淀而充填于样品裂隙,导致样品渗透率有所下降。  相似文献   
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Exploring the chemical characterization of dissolved organic matter (DOM) is important for understanding the fate of laterally transported organic matter in watersheds. We hypothesized that differences in water-extractable organic matter (WEOM) in soils of varying land uses and rainfall events may significantly affect the quality and the quantity of stream DOM. To test our hypotheses, characteristics of rainfall-runoff DOM and WEOM of source materials (topsoil from different land uses and gullies, as well as typical vegetation) were investigated at two adjacent catchments in the Loess Plateau of China, using ultraviolet–visible absorbance and excitation emission matrix fluorescence with parallel factor analysis (PARAFAC). Results indicated that land-use types may significantly affect the chemical composition of soil WEOM, including its aromaticity, molecular weight, and degree of humification. The PARAFAC analysis demonstrated that the soils and stream water were dominated by terrestrial/allochthonous humic-like substances and microbial transformable humic-like fluorophores. Shifts in the fluorescence properties of stream DOM suggested a pronounced change in the relative proportion of allochthonous versus autochthonous material under different rainfall patterns and land uses. For example, high proportions of forestland could provide more allochthonous DOM input. This study highlights the relevance of soils and hydrological dynamics on the composition and fluxes of DOM issuing from watersheds. The composition of DOM in soils was influenced by land-use type. Precipitation patterns influenced the proportion of terrestrial versus microbial origins of DOM in surface runoff. Contributions of allochthonous, terrestrially derived DOM inputs were highest from forested landscapes.  相似文献   
10.
To better understand the mechanisms relating to hydrological regulations of chemical weathering processes and dissolved inorganic carbon (DIC) behaviours, high-frequency sampling campaigns and associated analyses were conducted in the Yu River, South China. Hydrological variability modifies the biogeochemical processes of dissolved solutes, so major ions display different behaviours in response to discharge change. Most ions become diluted with increasing discharge because of the shortened reactive time between rock and water under high-flow conditions. Carbonate weathering is the main source of major ions, which shows strong chemostatic behaviour in response to changes in discharge. Ions from silicate weathering exhibit a significant dilution effect relative to the carbonate-sourced ions. Under high temperatures, the increased soil CO2 influx from the mineralisation of organic material shifts the negative carbon isotope ratios of DIC (δ13CDIC) during the high-flow season. The δ13CDIC values show a higher sensitivity than DIC contents in response to various hydrological conditions. Results from a modified isotope-mixing model (IsoSource) demonstrate that biological carbon is a dominant source of DIC and plays an important role in temporal carbon dynamics. Furthermore, this study provides insights into chemical weathering processes and carbon dynamics, highlighting the significant influence of hydrological variability to aid understanding of the global carbon cycle.  相似文献   
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