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1.
Marine ferromanganese nodules and crusts containing Mn, Cu, Ni and Co in the most promising resource-grade concentrations and quantities, together with Fe and Zn (all elements of biogeochemical importance) are found far from land on the deep seafloor of the Pacific Ocean. The biogeochemical, chemical and physical mechanisms contributing to their formation, distribution, abundance and – for these six elements – variability in their concentrations in these deposits, are the main focus of the present review. The mechanisms addressed include biological productivity, sedimentation types and rates, bottom water characteristics, the Calcium Carbonate Compensation Depth, the depth and intensity of the oxygen minimum zone, and biogeochemical characteristics of the six focal elements. Particular attention is given to comparisons between the deposits found in the north and the south Pacific, in order to present an overarching view of our current understanding of the mechanisms that apply to both nodules and crusts in both oceanic hemispheres, including examination of the possible existence of a marine ferromanganese oxide continuum. The renewed interest in the commercial exploitation of these deposits has stimulated a welcome increase in scientific research that is essential to informing the public discourse on seabed mining. We briefly reflect on the work addressed in this review in that context.  相似文献   
2.
The time it takes water to travel through a catchment, from when it enters as rain and snow to when it leaves as streamflow, may influence stream water quality and catchment sensitivity to environmental change. Most studies that estimate travel times do so for only a few, often rain-dominated, catchments in a region and use relatively short data records (<10 years). A better understanding of how catchment travel times vary across a landscape may help diagnose inter-catchment differences in water quality and response to environmental change. We used comprehensive and long-term observations from the Turkey Lakes Watershed Study in central Ontario to estimate water travel times for 12 snowmelt-dominated headwater catchments, three of which were impacted by forest harvesting. Chloride, a commonly used water tracer, was measured in streams, rain, snowfall and as dry atmospheric deposition over a 31 year period. These data were used with a lumped convolution integral approach to estimate mean water travel times. We explored relationships between travel times and catchment characteristics such as catchment area, slope angle, flowpath length, runoff ratio and wetland coverage, as well as the impact of harvesting. Travel time estimates were then used to compare differences in stream water quality between catchments. Our results show that mean travel times can be variable for small geographic areas and are related to catchment characteristics, in particular flowpath length and wetland cover. In addition, forest harvesting appeared to decrease mean travel times. Estimated mean travel times had complex relationships with water quality patterns. Results suggest that biogeochemical processes, particularly those present in wetlands, may have a greater influence on water quality than catchment travel times.  相似文献   
3.
针对银量法测定化学试剂氯化钠中氯化钠纯度,讨论了氯化钠纯度测定结果的测量不确定度的来源及评定方法,当K=2,氯化钠纯度测定结果的扩展不确定度为(99.70±0.64)%。  相似文献   
4.
在生产碳酸锂的工艺中,尤其除硫过程中,锂会伴随其它盐类析出,造成锂的大量夹带损失。因此盐湖高锂卤水中硫酸根的脱除对锂的高效富集,提高锂的收率有重大意义。研究以盐湖高锂卤水为原料,通过加入氯化钡,采用化学沉淀法除去卤水中的SO_4~(2-)。详细考察了原料配比(SO_4~(2-)与Ba~(2+)的摩尔比)、加料方式、加料时间、反应时间、搅拌速度和反应温度等操作条件对除硫率的影响;同时,重点研究了不同操作条件下锂的夹带损失率。结果表明:除硫的适宜条件为,原料配比1.3,并流加料,反应温度25℃,加料时间18 min,搅拌速度250 r/min,反应时间40 min;最终SO_4~(2-)的脱除率可达99.98%,锂的夹带损失率为17.77%。  相似文献   
5.
正1 Introduction Lithium resources are widely distributed in the oilfield brine from the Nanyishan district in the Qaidam Basin(Fan et al.,2007).The investigation of the thermodynamics and phase diagram of the brine system is valuable in providing the theoretic foundation and scientific guidance in the comprehensive exploitation of the mixture salts effectively.Comprehensive  相似文献   
6.
Isotope data of precipitation and groundwater in parts of the Voltaian Basin in Northern Ghana were used to explain the groundwater recharge regime in the area. Groundwater recharge is an important parameter in the development of a decision support system for the management and efficient utilization of groundwater resources in the area. It is therefore important to establish the processes and sources of groundwater recharge. δ18O and δ2H data for local precipitation suggest enrichment relative to the Global Meteoric Water Line (GMWL) and indicate that precipitation takes place at a relative humidity less than 100%. The groundwater data plot on an evaporation line with a slope of 5, suggesting a high degree of evaporative enrichment of the precipitation in the process of vertical infiltration and percolation through the unsaturated zone into the saturated zone. This finding is consistent with the observation of high evapotranspiration rates in the area and ties in with the fact that significant clay fraction in the unsaturated zone limits vertical percolation and thus exposes the percolating rainwater to the effects of high temperatures and low humidities resulting in high evapotranspiration rates. Groundwater recharge estimates from the chloride mass balance, CMB, method suggest recharge in the range of 1.8–32% of the annual average precipitation in the form of rainfall. The highest rates are associated with areas where open wells encourage significant amount of groundwater recharge from precipitation in the area. In the northern parts of the study area, groundwater recharge is lower than 12%. The recharge so computed through the application of the CMB methodology takes on a spatial distribution akin to the converse of the spatial pattern of both δ18O and δ2H in the area. As such, the locations of the highest recharge are associated with the most depleted values of the two isotopes. This observation is consistent with the assertion that low vertical hydraulic conductivities slow down vertical percolation of precipitation down to the groundwater water. The percolating precipitation water thus gets enriched in the heavier isotopes through high evapotranspiration rates. At the same time, the amount of water that finally reaches the water table is considerably reduced. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   
7.
农用地土壤中7种重金属可提取态的测定   总被引:1,自引:0,他引:1  
该文以氯化钙溶液进行提取,采用电感耦合等离子体质谱法和原子荧光光谱法,测定农用地土壤中Cd,As,Pb,Cr,Cu,Zn,Ni等7种重金属可提取态,检出限在0.003~0.06 mg/kg之间。该方法用于4个可提取态质控样品的测定,测定值与推荐值基本相符,测定的相对标准偏差(n=8)在3.3%~9.1%之间。基于800余件农用地土壤样品的测定数据,对7种重金属可提取态与土壤pH值及重金属总量之间的关系进行了初步考察。结果表明,7个重金属可提取态和总量关系无明显相关性,仅在土壤酸性条件下可提取态Cd与总量Cd呈正相关性。7种重金属提取率大小顺序为Cd>Zn>Ni>Cu,As>Pb>Cr,其中Cd,Zn,Ni,Cu,Pb的提取率随土壤pH值的增大而迅速下降,而As,Cr在土壤碱性条件下的提取率略高于中酸性条件下的提取率。  相似文献   
8.
某生产CaCl_2化工厂因环境问题被停止生产,厂区周边土壤和地下水受到不同程度的污染。为掌握污染土壤中污染因子的含量和地下水受污染情况,布置了土壤采样点和地下水监测点,利用厂区周边已有机民井进行水样采集,通过室内检测、分析研究等工作,得出在厂区周边土壤60~300cm深度范围内存在Ca~(2+),Cl~-富集,鉴于土壤的天然吸附和自净能力,目前条件下,厂区及周边地下水污染状况受影响较小。通过抽水试验、渗水试验和弥散试验,圈定了污染物的影响范围,查明了污染物的影响程度,并在此基础上进行了污染物影响变化情况的预测分析,为后续区域污染地块的风险评估和修复治理工作提供了数据支持。  相似文献   
9.
石天阳  余红发  麻海燕  李颖 《盐湖研究》2021,29(3):38-46, 55
氯氧镁水泥(Magnesium oxychloride cement, MOC)具有快凝、早强、高强、防火和不腐蚀玻璃纤维等优点,非常适合于制作玻璃纤维增强薄壁制品,在农业灌溉工程中具有良好的应用前景。采用XRD和TOPAS分析了新型抗水氯氧镁水泥制成内蒙古防渗渠的物相组成,探讨了氯氧镁水泥制品在自然环境的水化产物与相转变规律、以及相组成对强度的影响。结果表明,在水分缺少的条件下,氯氧镁水泥的水化产物主要为5Mg(OH)_2·MgCl_2·8H_2O(5·1·8)和Mg(OH)_2;在水分充足的条件下,水化产物主要为Mg(OH)_2和5·1·8,碳化产物为碳化氯氧化镁Mg(OH)_2·MgCl_2·2MgCO_3·6H_2O(1·1·2·6)和水菱镁矿4MgCO_3·Mg(OH)_2·4H_2O(4·1·4)。水化产物对强度有促进作用,而碳化产物会降低强度。通过10年的工程环境考验,证明新型氯氧镁水泥制品在环境中能够保持主要强度相5·1·8的稳定性,具有良好的长期力学性能。  相似文献   
10.
氯离子和硫酸根离子是海水中重要的无机阴离子,在研究海洋生态变化、海洋循环作用过程与海洋全球气候变化等领域具有重要的指示意义。其测定方法较多,但缺少相应的测试方法。本文对测定海水中Cl-,SO42-的离子色谱方法进行了优化,选用IonPacAS14碳酸盐选择性离子色谱柱,以3.5 mmol/L Na2CO3+1 mmol/L NaHCO3为流动相,可消除海水样品中碳酸盐及其他阴离子的干扰。该方法对Cl-检出限为0.29 mg/L,线性相关系数r2=0.999 2,对SO42-检出限为0.42 mg/L,线性相关系数r2=0.997 9。样品的加标回收率在95%~102%,Cl-和SO42-的相对标准偏差分别为1.92%和4.18%。该方法简便、迅速、灵敏、准确度高,可满足批量海水样品中Cl-与SO42-的准确测试。  相似文献   
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