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91.
线翼截断方式对大气辐射计算的影响 总被引:2,自引:0,他引:2
在大气辐射传输计算方法中,有3种基本方法,即,逐线积分方法,k-分布方法和带模式方法。其中,逐线积分方法是最精确的计算大气透过率的方法,本文根据透过率计算方式的不同,将逐线积分方法分为追线积分法和追点积分法。由于逐线积分计算需要耗费大量的计算时间,在大气遥感和大气探测业务中使用时,必须减少计算成本,提高计算速度。本文在追线积分法的基础上,给出了简化的逐线积分的基本方法,在保证同样计算精度的同时,大大提高了计算速度。对在精确的和简化的逐线积分下,不同线翼截断方式(CUTOFF)对吸收系数、大气透过率和冷却率的影响进行了更详细的探讨。通过数值试验发现,对谱线线翼的截断方式是影响辐射计算精度和计算速度的重要因子。在不同压力下,用CUTOFF=2计算的吸收系数误差最大;对CUTOFF=1,在大多数取样点上误差都小于2%;对CUTOFF=3或4,对绝大多数取样点上计算的吸收系数误差都在5%以内,但所用的计算时间却明显减少。大气低层的透过率对不同的计算方法和不同的线翼截断方式不敏感;对大气高层,无论是对精确的还是简化的逐线积分方法,当CUTOFF=2时的透过率结果与其他线翼截断方式的结果差别较大。通过比较,本文给出线翼截断的优选方案。 相似文献
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B. Smodiš M. L. Pignata M. Saiki E. CortÉs N. Bangfa B. Markert B. Nyarko J. Arunachalam J. Garty M. Vutchkov H. Th. Wolterbeek E. Steinnes M. C. Freitas A. Lucaciu M. Frontasyeva 《Journal of Atmospheric Chemistry》2004,49(1-3):3-13
The International Atomic Energy Agency (IAEA) organized a co-ordinated research project (CRP) on Validation and application of plants as biomonitors of trace element atmospheric pollution analysed by nuclear and related techniques involving 14 participating countries. The CRPs objective was to identify appropriate bioindicators for local and/or regional application and validate them for general air pollution monitoring. Activities included quantification studies, research into spatial and time resolution for particular organisms, and physiological studies. A number of suitable bioindicators were identified in different parts of the globe and tested during the CRP. Sampling strategies were reviewed and the recommended approach adopted by the group. Appropriate sample preparation procedures were assessed and harmonised to the degree allowed by different geographic and climatic conditions in the participating countries. Two interlaboratory comparison exercises were carried out on lichen and moss materials. Results confirmed definite improvement in analytical performance of the participating laboratories, but also revealed possible inconsistencies due to different sample processing procedures. Several monitoring surveys were carried out and consequently pollution maps drawn for extended areas or countries. Overall results confirmed applicability of lower plants for assessing the degree of atmospheric pollution and provided several countries with effective monitoring tools not used before. 相似文献
94.
Variation in the concentrations of iodine-129 (129I, T1/2=15.7 Myr), a low-level radioactive component of nuclear fuel waste, is documented in surface waters and depth profiles collected during 2001 along a transect from the Norwegian Coastal Current to the North Pole. The surface waters near the Norwegian coast are found to have 20 times higher 129I concentration than the surface waters of the Arctic Ocean. The depth profiles of 129I taken in the Arctic Ocean reveal a sharp decline in the concentration to a depth of about 300-500 m followed by a weaker gradient extending down to the bottom. A twofold increase in the 129I concentration is observed in the upper 1000 m since 1996. Based on known estimates of marine transient time from the release sources (the nuclear reprocessing facilities at La Hague, France, and Sellafield, UK), a doubling in the 129I inventory of the top 1000 m of the Arctic Ocean is expected to occur between the years 2001 and 2006. As 129I of polar mixed layer and Atlantic layer of the Arctic Ocean is ventilated by the East Greenland Current into the Nordic Seas and North Atlantic Ocean, further dispersal and increase of the isotope concentration in these regions will be encountered in the near future. 相似文献
95.
The annual and semi-annual variations of the ionosphere are investigated in the present paper by using the daytime F2 layer peak electron concentration (NmF2) observed at a global ionosonde network with 104 stations. The main features are outlined as follows. (1) The annual variations are most pronounced at magnetic latitudes of 40–60° in both hemispheres, and usually manifest as winter anomalies; Below magnetic latitude of 40° as well as in the tropical region they are much weaker and winter anomalies that are not obvious. (2) The semi-annual variations, which are usually peak in March or April in most regions, are generally weak in the near-pole regions and strong in the far-pole regions of both hemispheres. (3) Compared with their annual components, the semi-annual variations in the tropical region are more significant.In order to explain the above results, we particularly analyze the global atomic/molecular ratio of [O/N2] at the F2 layer peak height by the MSIS90 model. The results show that the annual variation of [O/N2] is closely related with that of NmF2 prevailing in mid-latitudes and [O/N2] annual variation usually may lead to the winter anomalies of NmF2 occurring in the near-pole region. Moreover, NmF2 semi-annual variations appearing in the tropical region also have a close relationship with the variation of [O/N2]. On the other hand, the semi-annual variations of NmF2 in the far-pole region cannot be simply explained by that of [O/N2], but the variation of the solar zenith angle may also have a significant contribution. 相似文献
96.
石墨炉原子吸收分光光度法测定土壤样品中痕量镉 总被引:2,自引:0,他引:2
研究了土壤样品中痕量镉的石墨炉原子吸收分光光度法测定最佳条件以及磷酸二氢铵与硝酸镁作基体改进剂对测定镉的基体改进效应,并比较了两种试样分解体系。方法检出限为0.01pg/L,精密度(RSD,n=8)为3.29%-7.69%,经国家一级标准物质分析验证,结果与标准值符合。 相似文献
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98.
高压密闭消解-电感耦合等离子体质谱法测定海洋沉积物中稀土元素 总被引:6,自引:3,他引:3
样品用HNO3-HF高压密闭消解,电感耦合等离子体质谱测定海洋沉积物中15种稀土元素。研究了消解方法、酸体系和质谱干扰对稀土元素测定的影响。结果表明,相比于电热板消解和微波消解,高压密闭消解具有酸用量少、消解完全、消解过程损失少等优点;HNO3-HF体系能有效地分解海洋沉积物样品;利用干扰离子校正方程,能有效地校正Ba和轻稀土元素所形成的多原子离子干扰。15种稀土元素的方法检出限为3~15 ng/g。使用水系沉积物标准物质GBW 07309和GBW 07311、海底沉积物标准物质GBW 07313进行验证,测定值与标准值基本吻合,相对标准偏差和相对误差均低于5%。方法用于长江口沉积物样品的测定,精密度(RSD,n=6)小于5%,加标回收率为95.8%~104%。该方法检出限低,精密度和准确度高,适用于大批海洋沉积物样品的分析。 相似文献
99.
在计算电感耦合等离子体质谱法测定饮用水中锶的浓度(x)时,由于标准系列配制和仪器检测过程中信号(y)漂移产生的不确定度会传递给最终的计算结果。普通的一次或多次线性拟合结果不能真实地反映对于x、y值都含误差的数据拟合情况。文章对标准曲线进行了双误差回归计算,从双误差回归线性方程推导出校准曲线拟合过程产生不确定度的计算公式,建立了方法检出限与曲线拟合参数(x、y、曲线截距和斜率)及其相关不确定度之间的关系式,依据误差连续传递公式及不确定度分量计算公式简化了合成不确定度的表达式。从合成不确定度计算公式中可得出,水样中锶含量的浓度越低,其对应的不确定度越大;标准系列配制过程不细致、仪器灵敏度低,方法检出限越差,与实际测试情况符合。 相似文献
100.
四种前处理方法对电感耦合等离子体质谱测定植物样品中27种微量元素的影响 总被引:6,自引:4,他引:2
采用HNO3-HClO4-HF常压消解、HNO3-H2O2-HF高压密闭消解、HNO3-H2O2微波消解,干法灰化后残渣用HNO3-HF-HClO4溶解等四种方法对植物样品进行前处理,使用电感耦合等离子体质谱(ICP-MS)对植物样品中的27种元素进行定量分析,探讨了不同前处理方法对ICP-MS测定植物样品中微量元素的影响。分析结果表明: HNO3-HClO4-HF常压消解使用大量试剂,污染环境,造成空白值高;在常压体系中HClO4的加入能提高样品的消解效率,但赶酸不完全,会造成复合离子对钒和砷的干扰;干法灰化过程中某些元素(硼、汞等)会损失;常压消解和高压密闭消解中加入HF能有效地提高铍、稀土、钇、钛、锑、铀等元素的回收率,但在蒸干赶HF的过程中,会造成硼和汞的损失,并且钢套的生锈会造成铬、镍空白值高。尽管没有一种方法能适用于所有元素的分析,但相比较而言,HNO3-H2O2微波消解体系操作简单,大部分元素(除铍、钛、锑、铋、稀土)能得到满意的结果,精密度(RSD)均小于10%(n=10),相对误差(RE)为-4.6%~13.6%。 相似文献