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141.
打水沟为宝兴河右岸的一级支流,位于宝兴县城城区,流域面积1.01 km2,主沟长度1.85 km,主沟比降640‰.受芦山“4·20”地震的影响,流域中下游直接引发了大量的崩滑体,加之地形陡峻,且位于青衣江-鹿头山暴雨区边缘,极容易发生泥石流.一旦发生泥石流,将会对沟口建筑和人员的安全造成巨大危害.通过对打水沟地震前后遥感影像的解译,结合野外考察,综合判定该沟为地震触发的潜在性泥石流沟.进一步分析估算,由于地震震动导致流域内发育6处崩塌体,总面积20375 m2,松散固体物质总量为15.20×l04m3.在分析泥石流形成条件与发展趋势的基础上,提出了打水沟泥石流减灾方案,并对泥石流排导槽梯形最佳过流横断面进行了设计.通过计算分析得到,在排泄设计标准的泥石流时,排导槽的最佳过流断面宽度为2.38 m,深度为2.23 m. 相似文献
142.
An Investigation of Digestion Methods for Trace Elements in Bauxite and Their Determination in Ten Bauxite Reference Materials Using Inductively Coupled Plasma‐Mass Spectrometry 下载免费PDF全文
Wen Zhang Liang Qi Zhaochu Hu Cunjiang Zheng Yongsheng Liu Haihong Chen Shan Gao Shenghong Hu 《Geostandards and Geoanalytical Research》2016,40(2):195-216
Trace elements from samples of bauxite deposits can provide useful information relevant to the exploration of the ore‐forming process. Sample digestion is a fundamental and critical stage in the process of geochemical analysis, which enables the acquisition of accurate trace element data by ICP‐MS. However, the conventional bomb digestion method with HF/HNO3 results in a significant loss of rare earth elements (REEs) due to the formation of insoluble AlF3 precipitates during the digestion of bauxite samples. In this study, the digestion capability of the following methods was investigated: (a) ‘Mg‐addition’ bomb digestion, (b) NH4HF2 open vessel digestion and (c) NH4F open vessel digestion. ‘Mg‐addition’ bomb digestion can effectively suppress the formation of AlF3 and simultaneously ensure the complete decomposition of resistant minerals in bauxite samples. The addition of MgO to the bauxite samples resulted in (Mg + Ca)/Al ratios ≥ 1. However, adding a large amount of MgO leads to significant blank contamination for some transition elements (V, Cr, Ni and Zn). The NH4HF2 or NH4F open vessel digestion methods can also completely digest resistant minerals in bauxite samples in a short period of time (5 hr). Unlike conventional bomb digestion with HF/HNO3, the white precipitates and the semi‐transparent gels present in the NH4HF2 and NH4F digestion methods could be efficiently dissolved by evaporation with HClO4. Based on these three optimised digestion methods, thirty‐seven trace elements including REEs in ten bauxite reference materials (RMs) were determined by ICP‐MS. The data obtained showed excellent inter‐method reproducibility (agreement within 5% for REEs). The relative standard deviation (% RSD) for most elements was < 6%. The concentrations of trace elements in the ten bauxite RMs showed agreement with the limited certified (Li, V, Cr, Cu, Zn, Ga, Sr, Zr and Pb) and information values (Co, Ba, Ce and Hf) available. New trace element data for the ten RMs are provided, some of which for the first time. 相似文献
143.
Sarah Gilbert Leonid Danyushevsky Philip Robinson Cora Wohlgemuth‐Ueberwasser Norman Pearson Dany Savard Marc Norman Jacob Hanley 《Geostandards and Geoanalytical Research》2013,37(1):51-64
A range of independently characterised reference materials (RMs) for LA‐ICP‐MS, used for the determination of the platinum‐group elements (PGE) and Au in a sulfide matrix, were analysed and compared: 8b, PGE‐A, NiS‐3, Po727‐T1, Po724‐T and the Lombard meteorite. The newly developed RM NiS‐3 was used as the RM for the calibration of all LA‐ICP‐MS analyses and the measured concentrations of the other RMs compared against their published concentrations. This data were also used to assess the consistency of concentrations calibrated against the different RMs. It was found that Po727‐T1 and 8b produced results that were comparable, within uncertainty, for all elements. Po727‐T1 also produced consistent results with NiS‐3 for all elements. All other RMs showed differences for some elements, especially Ru in Po724‐T, and Os, Ir and Au in PGE‐A. The homogeneity of the PGE and Au in each RM was assessed, by comparing the precision of multiple LA‐ICP‐MS spot analyses with the average uncertainty of the signal. Po724‐T, Po727‐T1 and the Lombard meteorite were found to be homogeneous for all elements, but 8b, PGE‐A and NiS‐3 were heterogeneous for some elements. This is the first direct comparison between a range of independently characterised PGE and Au LA‐ICP‐MS RMs. 相似文献
144.
煤的成因类型通过煤的有机显微组成、矿物成分等来体现。从微观研究的角度出发,以各子样的显微煤岩组分统计值、镜惰比(V/I)、骨基比(F/M)、矿物质含量为依据,对西山煤田屯兰煤矿7号煤进行成因类型划分,分为4类6型,即Ⅰ-①、Ⅲ-①、Ⅲ-②、Ⅳ-①、Ⅳ-②、Ⅴ-①。自下而上对煤层划分了23个成因分层。7煤层以Ⅳ类成因类型为主,沉积了覆水森林沼泽环境。 相似文献
145.
"4·20"芦山地震发生后,作为进出地震灾区的生命线工程省道S210芦山-宝兴段多处发生崩塌滚石等次生地质灾害,堵断交通,威胁来往群众的生命安全,严重影响了抗震救灾和灾后的恢复重建。通过对此路段进行崩塌灾害现场考察,得出此路段的崩塌灾害多发生在大于40°的坡体上,坡向为SW、W和NW,易发岩性为灰岩、砂岩、白云岩和砾岩,切割深度多大于16m。通过GIS进行因子叠加分析,将此路段划分为3级危险度区域,并根据芦山地震灾区崩塌滚石灾害成因机制、分布与活动特征、成灾方式与危害对象,提出了相应的防治对策与建议。 相似文献
146.
以冈底斯中段曲水县西南方向卡热乡一带出露的辉长岩为研究对象,进行了LA-ICP-MS锆石UPb测年以及全岩地球化学的系统测定,据此讨论岩石的成因及其构造意义。该辉长岩主要由单斜辉石和斜长石组成,辉长岩具有低硅、贫碱、富铝,中等富集轻稀土,富集大离子亲石元素,亏损高场强元素的地球化学特征,与岛弧和大陆边缘地区产出的高铝玄武岩化学组成十分相似,表明辉长岩原生岩浆为被俯冲改造的岩石圈幔源岩浆,在演化过程中受到了上地壳物质的混染。锆石LA-ICP-MS U-Pb年龄为49.01±0.51Ma(MSWD=0.41),指示岩体形成时代为始新世。卡热辉长岩具有显著亏损的锆石Hf同位素组成,εHf(t)值均为正值,分布在+10.88~+13.71之间,综合分析表明卡热辉长质侵入体可能为近期遭受俯冲板片析出流体交代作用的亏损地幔部分熔融的产物。结合区域构造演化史认为该岩体在冈底斯南缘的始新世期间存在着强烈的岩浆底侵和壳幔岩浆混合作用。 相似文献
147.
Ablation Characteristic of Ilmenite using UV Nanosecond and Femtosecond Lasers: Implications for Non‐Matrix‐Matched Quantification 下载免费PDF全文
Zhen Li Zhaochu Hu Detlef Günther Keqing Zong Yongsheng Liu Tao Luo Wen Zhang Shan Gao Shenghong Hu 《Geostandards and Geoanalytical Research》2016,40(4):477-491
Ilmenite (FeTiO3) is a common accessory mineral and has been used as a powerful petrogenetic indicator in many geological settings. Elemental fractionation and matrix effects in ilmenite (CRN63E‐K) and silicate glass (NIST SRM 610) were investigated using 193 nm ArF excimer nanosecond (ns) laser and 257 nm femtosecond (fs) laser ablation systems coupled to an inductively coupled plasma‐mass spectrometer. The concentration‐normalised 57Fe and 49Ti responses in ilmenite were higher than those in NIST SRM 610 by a factor of 1.8 using fs‐LA. Compared with the 193 nm excimer laser, smaller elemental fractionation was observed using the 257 nm fs laser. When using 193 nm excimer laser ablation, the selected range of the laser energy density had a significant effect on the elemental fractionation in ilmenite. Scanning electron microscopy images of ablation craters and the morphologies of the deposited aerosol materials showed more melting effects and an enlarged particle deposition area around the ablation site of the ns‐LA‐generated crater when compared with those using fs‐LA. The ejected material around the ns crater predominantly consisted of large droplets of resolidified molten material; however, the ejected material around the fs crater consisted of agglomerates of fine particles with ‘rough' shapes. These observations are a result of the different ablation mechanisms for ns‐ and fs‐LAs. Non‐matrix‐matched calibration was applied for the analysis of ilmenite samples using NIST SRM 610 as a reference material for both 193 nm excimer LA‐ICP‐MS and fs‐LA‐ICP‐MS. Similar analytical results for most elements in ilmenite samples were obtained using both 193 nm excimer LA‐ICP‐MS at a high laser energy density of 12.7 J cm?2 and fs‐LA‐ICP‐MS. 相似文献
148.
Weihan Li Jian‐Ming Zhu Decan Tan Guilin Han Zhouqiao Zhao Guangliang Wu 《Geostandards and Geoanalytical Research》2020,44(3):523-535
The high‐precision δ60/58Ni values of twenty‐six geological reference materials, including igneous rocks, sedimentary rocks, stream sediments, soils and plants are reported. The δ60/58Ni values of all samples were determined by double‐spike MC‐ICP‐MS (Nu Plasma III). Isotope standard solution (NIST SRM 986) and geological reference materials (BHVO‐2, BCR‐2, JP‐1, PCC‐1, etc.) were used to evaluate the measurement bias and intermediate precision over a period of six months. Our results show that the intermediate precision of Ni isotope determination was 0.05‰ (2s, n = 69) for spiked NIST SRM 986 and typically 0.06‰ for actual samples, and the δ60/58Ni NIST SRM 986 values were in excellent agreement with previous studies. Eighteen high‐precision Ni isotope ratios of geological reference materials are first reported here, and their δ60/58Ni values varied from ?0.27‰ to 0.52‰, with a mean of 0.13 ± 0.34‰ (2s, n = 18). Additionally, SGR‐1b (0.56 ± 0.04‰, 2s), GSS‐1 (?0.27 ± 0.06‰, 2s), GSS‐7 (?0.11 ± 0.01‰, 2s), GSD‐10 (0.46 ± 0.06‰, 2s) and GSB‐12 (0.52 ± 0.06‰, 2s) could potentially serve as candidate reference materials for Ni isotope fractionation and comparison of Ni isotopic compositions among different laboratories. 相似文献
149.
殷允强 《华东地质学院学报》2013,(4):442-448
把模糊集理论应用到n-序超群,在交换n-序超群中引入了(∈y,∈yVqδ)模糊n-序子超群和(∈y,∈yVqδ)模糊n-序可逆子超群的概念,并研究了其性质。 相似文献
150.
Wei‐Xin Lv Hao‐Ming Yin Meng‐Shu Liu Fang Huang Hui‐Min Yu 《Geostandards and Geoanalytical Research》2021,45(1):245-256
A dry ashing method is commonly used to remove organic material from samples prior to geochemical analysis. In the course of this study, the Cd isotope ratios of a series of soil and plant reference materials and samples were studied to evaluate the effect of the dry ashing method on measurement results of Cd isotope ratios. The samples were pre‐treated using the dry ashing method and high‐pressure bomb for comparison. The results show that the digestion using high‐pressure bombs did not lead to Cd loss, but using the dry ashing method would cause different proportions of Cd loss. The whole range of Cd isotope difference between two methods was from ?0.07‰ to 3.01‰. There was also an obvious difference in measured Cd isotope ratios from the same leaf sample pre‐treated independently by the dry ashing method, indicating that the amount of Cd loss and the effect on Cd isotope measurement during dry ashing is related to the properties of the samples. Therefore, dry ashing may not be appropriate for the removal of organic material in Cd isotope ratio measurement, especially for samples with high organic contents. The δ114/110Cd values of reference materials NIST SRM 1573a and GSD‐30 are reported for the first time in this study. 相似文献