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111.
The distribution of chlorophyll a(Chl a) and its relationships with physical and chemical parameters in different regions of the Bering Sea were discussed in July 2010. The results showed the seawater column Chl a concentrations were 13.41–553.89 mg/m2 and the average value was 118.15 mg/m2 in the study areas. The horizontal distribution of Chl a varied remarkably from basin to shelf in the Bering Sea. The regional order of Chl a concentrations from low to high was basin, slope, outer shelf, inner shelf, and middle shelf. The vertical distribution of Chl a was grouped mainly from single-peak type in basin, slope, outer shelf, and middle shelf, where the deep Chl a maxima(DCM) layer was observed at 25–50 m, 30–35 m, 36–44 m, and 37–47 m, respectively. The vertical distribution of Chl a mainly had three basic patterns: standard single-peak type, surface maximum type, and bottom maximum type in the inner shelf. The analysis also showed that the transportation of ocean currents may control the distribution of Chl a, and the effects were not simple in the basin of the Bering Sea. There was a positive correlation between Chl a and temperature, but no significant correlation between Chl a and nutrients. The Bering Sea slope was an area deeply influenced by slope current. Silicate was the factor that controlled the distribution of Chl a within parts of the water in the slope. Light intensity was an important environmental factor in controlling seawater column Chl a in the shelf, where Chl a was limited by nitrate rather than phosphate within the upper water. Meanwhile, there was a positive relationship between Chl a and salinity. Algal blooms broke out at Sta. B6 of the southwestern St. Lawrence Island and Stas F6 and F11 in the middle of the Bering Strait.  相似文献   
112.
An in vivo three-dimensional fluorescence method for the determination of algae community structure was developed by parallel factor analysis(PARAFAC) and CHEMTAX. The PARAFAC model was applied to fluorescence excitation-emission matrix(EEM) of 60 algae species belonging to five divisions and 11 fluorescent components were identified according to the residual sum of squares and specificity of the composition profiles of fluorescent. By the 11 fluorescent components, the algae species at different growth stages were classified correctly at the division level using Bayesian discriminant analysis(BDA). Then the reference fluorescent component ratio matrix was constructed for CHEMTAX, and the EEM–PARAFAC–CHEMTAX method was developed to differentiate algae taxonomic groups. The correct discrimination ratios(CDRs) when the fluorometric method was used for single-species samples were 100% at the division level, except for Bacillariophyta with a CDR of 95.6%. The CDRs for the mixtures were above 94.0% for the dominant algae species and above 87.0% for the subdominant algae species. However, the CDRs of the subdominant algae species were too low to be unreliable when the relative abundance estimated was less than 15.0%. The fluorometric method was tested using the samples from the Jiaozhou Bay and the mesocosm experiments in the Xiaomai Island Bay in August 2007. The discrimination results of the dominant algae groups agreed with microscopy cell counts, as well as the subdominant algae groups of which the estimated relative abundance was above 15.0%. This technique would be of great aid when low-cost and rapid analysis is needed for samples in a large batch. The fluorometric technique has the ability to correctly identify dominant species with proper abundance both in vivo and in situ.  相似文献   
113.
陈海杰  于兆水  邢夏 《物探与化探》2014,(2):393-395,401
为了简化测量植物中汞含量的方法,提高灵敏度及结果的可信度,实验采用微波消解植物样品的办法,使样品经氯化亚锡还原,再用冷原子荧光测定出植物样品中汞的含量。确定了消解样品的方法和微波消解样品的条件,优化了仪器的最佳工作参数。方法检出限0.30×10-9(稀释因子100倍),精密度(n=12)在2.09%~6.05%,加标回收率94.1%~105.5%,方法经生物国家一级标准物质验证方法准确可靠。  相似文献   
114.
正1 Introduction Annually laminated(varve)sedimentary deposits are considered as one of the most important archives,since they offer precise temporal information(years)in combination with high time resolutions.Bottom sediments of the lakes contain detailed geochemical information on  相似文献   
115.
氯化亚锡还原冷蒸汽无色散原子荧光光谱法测定痕量汞,采用硫酸、双氧水、王水逐次加入低温分析样品,可以保证样品分解完全又可避免汞的损失。汞的检出限为6.0×10~(-10)g,精密度RSD%=4.1。该方法操作简便,快速、准确、费用低,可应用于大批量地球化学样品的分析。  相似文献   
116.
Continuous monitoring of dissolved organic matter (DOM) character and concentration at hourly resolution is rare, despite the importance of analysing organic matter variability at high‐temporal resolution to evaluate river carbon budgeting, river water health by detecting episodic pollution and to determine short‐term variations in chemical and ecological function. The authors report a 2‐week experiment performed on DOM sampled from Bournbrook, Birmingham, UK, an urban river for which spectrophotometric (fluorescence, absorbance), physiochemical (dissolved organic carbon [DOC], electrical conductivity, pH) and isotopic (D/H) parameters have been measured at hourly frequency. Our results show that the river had sub‐daily variations in both organic matter concentration and characteristics. In particular, after relatively high‐magnitude precipitation events, organic carbon concentration increased, with an associated increase in intensity of both humic‐like and tryptophan‐like fluorescence. D/H isotopic ratio demonstrates different hydrological responses to different rainfall events, and organic matter character reflects this difference. Events with precipitation < 2 mm typically yielded isotopically heavy water with relatively hydrophilic DOM and relatively low specific absorbance. Events with precipitation > 2 mm had isotopically lighter water with higher specific absorbance and a decrease in the proportion of microbially derived to humic‐like fluorescence. In our heavily urbanized catchment, we interpret these signals as one where riverine DOM is dominated by storm sewer‐derived ‘old’ organic matter at low‐rainfall amounts and a mixed signal at high‐precipitation amounts where ‘event’ surface runoff‐derived organic matter dominate during storm sewer and combined sewer overflow routed DOM. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   
117.
Fluorescence lifetime provides a third independent dimension of information for the resolution of totalluminescence spectra of multicomponent mixtures.The incorporation of this parameter into theexcitation-emission matrix(EEM)by the phase modulation technique results in a three-dimensionalexcitation-emission-frequency array (EEFA).Multicomponent analysis based on the three-dimensionalEEFA brings a qualitative change for the resolved spectra,i.e.individual spectra can be uniquely resolved,which is impossible with any two-dimensional analysis.In this paper we present a method for analyzingthe EEFA.We show mathematically that with the three-dimensional analysis of the EEFA individualspectra and lifetimes can be obtained.Our algorithm is developed in mathematical detail and isdemonstrated by its application to a two-component mixture.  相似文献   
118.
叶绿素荧光是光合作用的有效探针,可用于海洋浮游植物的监测与定量评估。太阳诱导叶绿素荧光覆盖可见光—近红外650—800 nm,在~685 nm与~740 nm表现出两个形态不同的荧光峰特征。基于~685 nm荧光峰的叶绿素浓度反演算法较为成熟,但在高悬浮物和高叶绿素浓度的水体中,算法的有效性不足。基于叶绿素荧光在氧气吸收谱段(O2-A)的填充作用,水体遥感反射率光谱~761 nm峰值中包含有太阳诱导叶绿素荧光信号,能用于水体叶绿素浓度的估算,但该反射峰形态特征还取决于传感器的光谱分辨率。本研究基于不同光谱分辨率的大气吸收谱线特征,模拟了水体遥感反射率光谱(750—775 nm)上太阳诱导叶绿素荧光的信号响应特征;分析了利用遥感反射率(~761 nm)计算叶绿素荧光的原理,阐明了不同光谱分辨率条件下水体叶绿素荧光信号在反射光谱上的形态变化规律。采用水面以上测量法获取的离水光谱辐亮度,包含了水面的菲涅尔反射信号,由于真实的菲涅尔系数难以准确测量,这给基于~761 nm处遥感反射率峰值的荧光信号估算带来不确定性影响。研究表明,假定菲涅尔系数为0时,虽然~761 nm叶绿素荧光信号与其浓度具有较好的线性统计关系,但却带来较大的不确定性;这种不确定的影响,在低浓度叶绿素水体中表现明显,在高浓度叶绿素水体中,影响相对较小;准确估算菲涅尔系数,有助于减少这种不确定性影响。对基于遥感反射率~761 nm叶绿素荧光信号的深入探讨,将能推动未来水体叶绿素荧光的识别与利用。  相似文献   
119.
硒元素是人体必需的微量元素之一,食用富硒农产品是人体获取和补充硒元素的主要途径,调查区域硒地球化学特征是有效地利用富硒土地资源以及开发富硒农副产品的重要依据。本文选择四川省昭觉县域内较为重要的农耕乡镇采集表层土壤样品,采用原子荧光光谱法、X射线荧光光谱法、电感耦合等离子体质谱/发射光谱法等方法测定1328件土壤、19件玉米及20件土豆中硒等地球化学指标含量,利用相关分析与统计学等方法,结合距离加权反比插值法,探讨研究区硒含量、分布和影响因素等地球化学特征,评价土壤与作物的富硒情况及安全性。结果表明:(1)研究区表层土壤硒含量范围为0.04~1.50mg/kg,平均值为0.33mg/kg,划定富硒土壤面积为7.23km~2,占全区土壤面积的30.31%,玄武岩发育的土壤硒含量最高,平均值为0.4mg/kg,表明区内地质背景与土壤硒含量密切相关,区内富硒土壤主要受含玄武岩夹苦橄岩、凝灰质砂泥岩的峨眉山玄武岩组地层控制;(2)不同的用地类型和土壤类型对硒元素的富集能力不同,人为农业活动导致土壤对硒的吸附能力下降,黄棕壤土层中黏粒或铁氧化物等易与硒结合富集;酸性土壤中硒含量与pH值成反比;土壤...  相似文献   
120.
Cd Te量子点具有荧光强度高和稳定性好的优点,应用Cd Te量子点荧光猝灭法分析基体复杂的样品,需要有效分离对测定干扰的金属元素和高效富集待测元素。本文以巯基乙酸(TGA)作稳定剂,采用水相合成法制备了巯基乙酸修饰的Cd Te量子点,基于镍离子在p H=10.0硼砂缓冲溶液中对Cd Te量子点的荧光具有较强猝灭作用,建立了一种测定赤泥中痕量镍的荧光光度方法。荧光猝灭反应的最佳实验条件为:Cd Te量子点的浓度3.0×10-4mol/L,反应温度为室温,反应时间10 min,在此条件下镍离子浓度在2.0×10-7~7.8×10-5mol/L范围内与Cd Te量子点的相对荧光强度呈良好的线性关系;方法检出限为1.5×10-7mol/L。本方法针对Fe3+、Co2+、Cu2+等主要基体金属元素允许量低的问题,采用25%的2-羟基-4-仲辛氧基二苯甲酮肟(N530)磺化煤油萃取回收滤液中的Ni2+,镍回收率达到99%以上;赤泥中痕量镍的测定结果与催化光度法相符,加标回收率为98.3%-104.2%。  相似文献   
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