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891.
The southern Changjiang River Estuary has attracted considerable attention from marine scientists because it is a highly biologically active area and is biogeochemically significant.Moreover,land-ocean interactions strongly impact the estuary,and harmful algal blooms(HABs) frequently occur in the area.In October 2010 and May 2011,water samples of chromophoric dissolved organic matter(CDOM) were collected from the southern Changjiang River Estuary.Parallel factor analysis(PARAFAC) was used to assess the samples' CDOM composition using excitation-emission matrix(EEM) spectroscopy.Four components were identified:three were humic-like(C1,C2 and C3) and one was protein-like(C4).Analysis based on spatial and seasonal distributions,as well as relationships with salinity,Chl a and apparent oxygen utilization(AOU),revealed that terrestrial inputs had the most significant effect on the three humic-like Components C1,C2 and C3 in autumn.In spring,microbial processes and phytoplankton blooms were also important factors that impacted the three components.The protein-like Component C4 had autochthonous and allochthonous origins and likely represented a biologically labile component.CDOM in the southern Changjiang River Estuary was mostly affected by terrestrial inputs.Microbial processes and phytoplankton blooms were also important sources of CDOM,especially in spring.The fluorescence intensities of the four components were significantly higher in spring than in autumn.On average,C1,C2,C3,C4 and the total fluorescence intensity(TFI) in the surface,middle and bottom layers increased by123%–242%,105%–195%,167%–665%,483%–567% and 184%–245% in spring than in autumn,respectively.This finding corresponded with a Chl a concentration that was 16–20 times higher in spring than in autumn and an AOU that was two to four times lower in spring than in autumn.The humification index(HIX) was lower in spring that in autumn,and the fluorescence index(FI) was higher in spring than in autumn.This result indicated that the CDOM was labile and the biological activity was intense in spring. 相似文献
892.
为降低孕镶金刚石复合材料的烧结温度,采用脉冲电流烧结法,对纳米Cu粉末、纳米WC-12%Co粉末及常规的63^#配方胎体进行了烧结实验。结果表明,纳米Cu粉在700℃可实现致密化,纳米WC-12%Co粉末、63^#配方胎体可分别在1100℃、850℃实现致密化,均大大低于常规烧结方法的烧结温度,还起到保护金刚石、降低能耗、增加石墨模具寿命的作用。 相似文献
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894.
Atsushi Okamoto Shuhei Tanaka Masaoki Uno Otgonbayar Dandar Kazuki Yoshida 《Island Arc》2024,33(1):e12519
Thermogravimetric (TG) analyses were used to characterize the products and quantify the extent of serpentinization as a stepwise weight loss during heating (TG loss) or its derivative (DTG). Multivariate analyses are powerful tools for extracting information from complicated spectrum data; however, no studies have applied them to characterize serpentinites. In this study, hydrothermal experiments of olivine-H2O, olivine–orthopyroxene-H2O and orthopyroxene-H2O were conducted at 250–400°C and under vapor-saturated pressure. The product minerals observed were serpentine+brucite+magnetite in the olivine-H2O experiments and serpentine±talc in the orthoyroxene-H2O and olivine-orthopyroxene-H2O experiments. These results are consistent with those of previous studies; however, the positions and width of DTG peaks for individual minerals were varied depending on the experimental conditions. To extract systematics from the TG spectra, non-negative matrix factorization (NMF), an unsupervised machine learning technique, was applied to the DTG spectra of the experimental products. NMF revealed that the DTG profiles were explained by a linear combination of six basis spectra, which corresponded to the characteristic products, including three types of serpentine minerals (low-, medium-, and high-T), two types of brucite (low-and high-T), two type of talc (talc+serpentine mixture, well-crystallized talc) with different crystallinity, and noise during the TG measurement. Systematic changes in the factor loading revealed that, in the olivine-H2O systems, the products changed from medium-T serpentine+low-T brucite to high-T serpentine+high-T brucite as serpentinization progressed. In the olivine-orthopyroxene system, low-T serpentine or poorly crystallized talc+serpentine mixture was initially formed, followed by the formation of well-crystallized talc, resulting in dehydration. Applying NMF to DTG showed the mineralogical differences between olivine and orthopyroxene systems and increases of the crystallinity during the progress of serpentinization, suggesting its potential for characterizing various serpentinites within oceanic lithospheres that suffer from several stages of alteration and weathering at different temperatures. 相似文献
895.
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897.
利用小波包分析在时域和频域同时具有良好的局部化特性,对信号进行小波包变换后,用谱矩阵法计算质点的空间运动特性,构造相应的滤波函数,对分解后的信号进行滤波,将滤波结果用逆小波包变换进行重构,实现了滤除干扰、保留有用信号的目的,取得了非常满意的效果。 相似文献
898.
矩阵分解是矩阵计算的重要工具。针对整体最小二乘、子集选择、子空间计算等实际问题,通过比较应用RRURVD和SVD两种分解方法得到的结果,说明RRURVD是SVD的良好替代方法。 相似文献
899.
Aaron M. Jubb Mark A. Engle Jessica M. Chenault Madalyn S. Blondes Cloelle G. Danforth Colin Doolan Tanya J. Gallegos Dan Mueller Jenna L. Shelton 《Geostandards and Geoanalytical Research》2020,44(2):385-397
Waters co‐produced during petroleum extraction are the largest waste streams from oil and gas development. Reuse or disposal of these waters is difficult due to their high salinities and the sheer volumes generated. Produced waters (PWs) may also contain valuable mineral commodities. While an understanding of produced water trace element composition is required for evaluating the associated resource and waste potential of these materials, measuring trace elements in brines is challenging due to the dilution requirements of typical methods. Alternatively, inductively coupled plasma‐optical emission spectrometry (ICP‐OES) has shown promise as being capable of direct measurements of trace elements within PWs with minimal dilution. Here, we evaluate direct ICP‐OES trace element quantification in PWs for seventeen trace elements (As, Al, Ba, Be, Cd, Cr, Co, Cu, Hg, Mo, Ni, Pb, Rb, Sb, U, V and Zn) within fifteen PWs from five U.S. continuous reservoirs. The total analytical uncertainties associated with the trace element levels determined using ICP‐OES were estimated to be better than ± 30% (2s) except for Rb, which could not be determined due to ionisation interferences. The ICP‐OES results are compared with trace element levels determined using inductively coupled plasma‐mass spectrometry from the same samples. Our results demonstrate the potential for direct analysis of high‐salinity waters using ICP‐OES with minimal dilution and provide trace element concentrations in waters from several important U.S. petroleum‐generating reservoirs where available data are sparse. 相似文献
900.