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441.
Meretrix meretrix Linnaeus has long been used as traditional Chinese medicine in oriental medicine.The angiogentic activity of the extract of M.meretrix was investigated in this study,using human umbilical vein endothelial cells(HUVECs).Extract of M.meretrix Linnaeus(AFG-25) was prepared with acetone and ethanol precipitation,and further separated by Sephadex G-25 column.The results show that AFG-25 promoted proliferation,migration,and capillary-like tube formation in HUVECs,and in the presence of eNOS inhibitor NMA,the tube formation induced by AFG-25 is inhibited significantly.Moreover,AFG25 could also promote the activation of endothelial nitric oxide synthase(eNOS) and the resultant elevation of nitric oxide(NO) production.The results suggested that M.meretrix contains active ingredients with angiogentic activity and eNOS/NO signal pathway is in part involved in the proangiogenesis effect induced by AFG-25.  相似文献   
442.
锰银氧化矿选冶工艺的研究现状及进展   总被引:1,自引:0,他引:1  
锰银氧化矿在中国是一种重要的矿床类型 ,但在目前经济技术条件下仍属于难选冶和无商业价值的矿石类型。文章对国内外锰银氧化矿选冶技术的研究现状和进展进行了比较全面的评述  相似文献   
443.
We observed a direct reaction of metallic iron with water to form iron hydride and iron oxide, 3Fe + H2O–>2FeHx + FeO, at pressures from 6 GPa to 84 GPa and temperatures above 1,000 K in diamond anvil cell (DAC). Iron hydride is dhcpFeHx or -FeHx, and iron oxide has the rhombohedral or B1 structure at pressures at least up to 37 GPa. The formation of an assembly composed of dhcpFeHx and FeO with the B8 structure was observed at 84 GPa. In primordial Earth, water formed by dehydration of the low temperature primitive materials reacts with metallic iron in the high temperature component to form iron hydride FeHx and iron oxide FeO. The former would be incorporated in the iron forming the core. Thus hydrogen could be an important element of the Earths core. This reaction would be essential for transport of hydrogen into the core in the accretion stage of the Earth.  相似文献   
444.
对一氧化氮在浮游植物中的研究进展进行了归纳,总结了一氧化氮对浮游植物生长的影响,探讨了浮游植物中一氧化氮的产生机制,并对今后的研究重点提出展望。  相似文献   
445.
本文综述了 NO在生物体和大气中的作用 ,重点阐述了 NO的各种测定方法 ,尤其是电化学法 ,并对今后的发展提出展望  相似文献   
446.
Chemical amplification, CA, a method commonly used for the detection of peroxy radicals, HO2 and RO2, was found to be sensitive towards ClOx (Cl+ClO+OClO) as well. ClOx is reduced by NO to Cl atoms which react with carbon monoxide in the presence of O2. The reaction sequence thus initiated oxidizes CO to CO2 and NO to NO2, with a chain length of 300 ± 60. This allows the atmospheric ClOx content to be measured under ambient conditions with a detection limit of better than 1 ppt. In parallel peroxy radicals are indicated with a chain length of 160 ± 15. Chemical amplification is not specific and does not indicate which radical chain it is seeing. Identification relies solely on plausibility. During the ARCtic Tropospheric Ozone Chemistry (ARCTOC) campaign in spring 1995 and 1996 the CA technique was used at Ny-Ålesund. ClOx at mixing ratios of up to 2 ppt were found in the boundary layer under certain conditions. The low concentrations of ClOx indicate that the arctic boundary ozone depletion is mainly driven by bromine.  相似文献   
447.
现代黄河三角洲ZK226孔岩心的~(210)Pb、Al、Fe、Mn和Cu的地球化学表明,沉积物的粒度是控制上述元素的主要因素,这些元素与粒度的相关性是~(210)Pb>Fe>Al>Mn>Cu。粘土和Fe的水合氧化物是吸附~(210)Pb的主要组分。标准化后的~(210)Pb_ex,与Al、Fe,Mn和Cu的比值对黄河中上游流域的土壤侵蚀情况具有良好的指示意义,这为建立黄河中上游流域的土壤侵蚀模式打下了必要的基础。  相似文献   
448.
以共和盆地东部风成沉积剖面(MS剖面)磁化率为依据,运用四次回归方程重建了剖面形成时的年均气温和降水量,确定近12 ka以来共和盆地年均温度–0.37℃~5.09℃,多年平均温度为2.5℃,降水量267.91~550.77 mm,多年平均降水量为418.62 mm。对常量元素氧化物(SiO_2、Al_2O_3和Fe_2O_3)含量进行分析,结果表明:1)古土壤层SiO_2含量均低于风成砂层, Al_2O_3和Fe_2O_3含量均高于风成砂层; 2)风成砂层SiO_2含量S3>S5>S1,Al_2O_3和Fe_2O_3含量S5>S3>S1,揭示S3层形成时期冷干, S5层次之, S1层干旱程度较弱;土壤层SiO_2含量S4>S2>S6, Al_2O_3和Fe_2O_3含量为S6>S2>S4,表明S6形成时期气候温湿, S2层次之, S4层温湿程度较低; 3)分层氧化物变异系数大小表明S2和S6层形成时气候波动剧烈, S1和S3层形成时期气候较稳定。以常量元素氧化物含量、温度和降水为依据,结合14C测年,重建了近12 ka以来共和盆地环境演变过程:11.9 ka BP以前为凉干期,11.9~9.7 ka BP为温湿期, 9.7~8.0 ka BP为冷干期, 8.0~4.8 ka BP为暖湿期, 4.8~2.9 ka BP为凉干期, 2.9 ka BP以来为温润期。马四剖面记录的环境演变过程与青藏高原其他区域环境演变过程具有相似性,表明共和盆地环境演变与区域环境变化具有同步性。  相似文献   
449.
海洋沉积物中氧化亚铁的分析测定   总被引:2,自引:0,他引:2  
郑凯清  张仲平 《岩矿测试》1999,18(3):198-200
海洋沉积物试样用H2O2-HAc浸取,用以除去干扰测定FeO的锰化合物和硫化珠,并以H2SO3-Na2SO3混合溶液破坏过乘的H2O2,不需过滤分离,即可用HF-H2SO4分解试样,K2Cr2O7标准溶液滴定FeO。方法经海洋沉积物国家标准物质分析验证,结果与参考值相符,RSD为6.33%。  相似文献   
450.
Nutrient-rich exfiltrating groundwater may impose a heavy phosphate load on surface water systems. However, iron oxides that bind PO4 precipitate fast upon oxygenation at neutral pH and PO4 may also become bound in Ca precipitates following upon pH increase, so load estimates based on conservative behaviour during exfiltration will be overestimates. Aeration experiments using natural groundwater were performed to characterise the immobilisation of PO4 within one day after aeration started. Groundwaters having a wide variety in composition, were sampled in the coastal lowlands of the Western Netherlands. Three models were considered to describe the fast binding of PO4 by Fe oxide type phases that form upon the oxygenation of dissolved Fe(II), each based on a different concept. The concepts were surface complexation, solid-solution precipitation and two-mineral precipitation. When the experimental data were compared with model results, all three models were found to be inadequate. Frequently, more immobilisation of PO4 occurred than could be explained by binding to a Fe oxide type of phase alone. Uptake by Ca phosphates and/or Ca carbonates must additionally have played a role; alternatively, a non-ideal phase consisting of Ca, Fe and PO4 precipitated upon oxygenation and CO2 degassing. A predictive multiple regression model with two primary variables that reflect the driving forces for PO4 immobilisation was deduced that describes immobilisation of phosphate after aeration of anoxic groundwater. The two primary variables are the log value of the groundwater Fe to PO4 molar ratio and the saturation state for hydroxyapatite after the CO2 degassing of groundwater. The model is useful for calculating the PO4 load of surface water from exfiltration groundwater, taking into account fast immobilisation (<1 day) during exfiltration.  相似文献   
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