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81.
The two drill holes, which penetrated sub‐horizontal rare earth element (REE) ore units at the Nechalacho REE in the Proterozoic Thor Lake syenite, Canada, were studied in order to clarify the enrichment mechanism of the high‐field‐strength elements (HFSE: Zr, Nb and REE). The REE ore units occur in the albitized and potassic altered miaskitic syenite. Zircon is the most common REE mineral in the REE ore units, and is divided into five types as follows: Type‐1 zircon occurs as discrete grains in phlogopite, and has a chemical character similar to igneous zircon. Type‐2 zircon consists of a porous HREE‐rich core and LREE–Nb–F‐rich rim. Enrichment of F in the rim of type‐2 zircon suggests that F was related to the enrichment of HFSE. The core of type‐2 zircon is regarded to be magmatic and the rim to be hydrothermal in origin. Type‐3 zircon is characterized by euhedral to anhedral crystals, which occur in a complex intergrowth with REE fluorocarbonates. Type‐3 zircon has high REE, Nb and F contents. Type‐4 zircon consists of porous‐core and ‐rim, but their chemical compositions are similar to each other. This zircon is a subhedral crystal rimmed by fergusonite. Type‐5 zircon is characterized by smaller, porous and subhedral to anhedral crystals. The interstices between small zircon grains are filled by fergusonite. Type‐4 and type‐5 zircon grains have low REE, Nb and F contents. Type‐1 zircon is only included in one unit, which is less hydrothermally altered and mineralized. Type‐2 and type‐3 zircon grains mainly occur in the shallow units, while those of type‐4 and type‐5 are found in the deep units. The deep units have high HFSE contents and strongly altered mineral textures (type‐4 and type‐5) compared to the shallow units. Occurrences of these five types of zircon are different according to the depth and degree of the hydrothermal alteration by solutions rich in F and CO3, which permit a model for the evolution of the zircon crystallization in the Nechalacho REE deposit as follows: (i) type‐1 (discrete magmatic zircon) is formed in miaskitic syenite. (ii) LREE–Nb–F‐rich hydrothermal zircon formed around HREE‐rich magmatic zircon (type‐2). (iii) type‐3 zircon crystallized through the F and CO3‐rich hydrothermal alteration of type‐2 zircon which formed the complex intergrowth with REE fluorocarbonates; (iv) the CO3‐rich hydrothermal fluid corroded type‐3, forming REE–Nb‐poor zircon (type‐4). Niobium and REE were no longer stable in the zircon structure and crystallized as fergusonite around the REE–Nb‐leached zircon (type‐4); (v) type‐5 zircon is formed by the more CO3‐rich hydrothermal alteration of type‐4 zircon, suggested by the fact that type‐4 and type‐5 zircon grains are often included in ankerite. Type‐3 to type‐5 zircon grains at the Nechalacho REE deposit were continuously formed by leaching and/or dissolution of type‐2 zircon in the presence of F‐ and/or CO3‐rich hydrothermal fluid. These mineral associations indicate that three representative hydrothermal stages were present and related to HFSE enrichment in the Nechalacho REE deposit: (i) F‐rich hydrothermal stage caused the crystallization of REE–Nb‐rich zircon (type‐2 rim and type‐3), with abundant formation of phlogopite and fluorite; (ii) F‐ and CO3‐rich hydrothermal stage led to the replacement of a part of REE–Nb–F‐rich zircon by REE fluorocarbonate; and (iii) CO3‐rich hydrothermal stage resulted in crystallization of the REE–Nb–F‐poor zircon and fergusonite, with ankerite. REE and Nb in hydrothermal fluid at the Nechalacho REE deposit were finally concentrated into fergusonite by way of REE–Nb–F‐rich zircon in the hydrothermally altered units.  相似文献   
82.
The aim of this study was to evaluate total mercury concentration and its lithogenic and exogenic fractions in some calcareous soils of western Iran, where water contamination and bioaccumulation of mercury have been reported in the bottomland’s reservoir. In particular, we investigated soil physico-chemical properties and weathering conditions related to lithogenic and exogenic fractions of mercury for two groups of calcareous soils with a known comparative pedological evolution and weathering condition that was evident in the presence or absence of underlying layers of accumulated clay. Our results showed that the total mercury content of the studied soils ranged from 45.40 to 830.36 with a mean of 486.81 μg kg?1. Furthermore, calculation of mercury fractions revealed that lithogenic and exogenic fractions vary slightly according to the three reference elements (Fe, U and Nb) used in the calculations for the two groups of studied soils. The results also illustrated that most of the mercury content is of exogenic origin; therefore, total mercury variations are closely related to the content of exogenic mercury, while the lithogenic fraction exhibited no relationship with total mercury concentration. Moreover, application of the weathering indexes of Parker and the CaO/ZrO2 molar ratio supported the dependence of lithogenic mercury accumulation on weathering intensity in the studied calcareous soils. However, the significance of this relationship is stronger for more weathered calcareous soils; in such cases, fine-particle fractions are more developed, which encourages carrier phases such as organic materials and iron oxyhydroxides to become involved in more efficient fixation of mercury. Nevertheless, the formation of underlying layers of accumulated clay, i.e. argillic horizons, may restrain fixation of exogenic mercury by limiting its atmospheric input.  相似文献   
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86.
The SOLAR-A spacecraft has spectroscopic capabilities in a wide energy band from soft X-rays to gamma-rays. The Wide Band Spectrometer (WBS), consisting of three kinds of spectrometers, soft X-ray spectrometer (SXS), hard X-ray spectrometer (HXS) and gamma-ray spectrometer (GRS), is installed on SOLAR-A to investigate plasma heating, high-energy particle acceleration, and interaction processes. SXS has two proportional counters and each counter provides 128-channel pulse height data in the 2–30 keV range every 2 s and 2-channel pulse count data every 0.25 s. HXS has a NaI scintillation detector and provides 32-channel pulse height data in the 20–400 keV range every 1 s and 2-channel pulse count data every 0.125 s. GRS has two identical BGO scintillation detectors and each detector provides 128-channel pulse height data in the 0.2–10 MeV range every 4 s and 4-channel pulse count data (0.2–0.7, 0.7–4, 4–7, and 7–10 MeV) every 0.25–0.5 s. In addition, each of the BGO scintillation detectors provides 16-channel pulse height data in the 8–100 MeV range every 4 s and 2-channel pulse count data (8–30 and 30–100 MeV) every 0.5 s. The SXS observations enable one to study the thermal evolution of flare plasma by obtaining time series of electron temperatures and emission measures of hot plasma; the HXS observations enable one to study the electron acceleration and heating mechanisms by obtaining time series of the electron spectrum; and the GRS observations enable one to study the high-energy electron and ion acceleration and interaction processes by obtaining time series of electron and ion spectra.After the launch the name of SOLAR-A has been changed to YOHKOH.  相似文献   
87.
A balloon-borne gemanium spectrometer was flown in an attempt to detect line-emission from Cyg X-1 and the Crab nebula in the energy range 30–270 keV. The experiment was carried out on 29–30 September, 1982. A line feature at 145 keV was observed from Cyg X-1. The intensity is (1.34±0.31)×10–2 photons cm–2 s–1 and the width is 14.3 keV FWHM. From the Crab nebula, a weak line feature with 1.8 excess was found around 78 keV.  相似文献   
88.
Measurements of the concentrations of H2O2 and methyl hydroperoxide (MHP), O3, and SO2 over Imizu City, Toyama Prefecture, Japan were performed in March using a helicopter. H2O2 concentrations were higher at an altitude of approximately 2,400 m (8,000 ft). The H2O2 concentrations (< 0.8 ppb) in the spring were much lower than those observed during the summer observations. MHP was also higher in the high-altitude atmosphere. Lower concentrations of H2O2 were observed when high air pollutants were actively transported from Asian continent. The concentrations of H2O2 were mostly lower than those of SO2; this condition is called oxidant limitation. If H2O2 concentration rises in cold months, the acidification of cloud water may be accelerated at high elevations in central Japan where air pollution is actively transported.  相似文献   
89.
Chemical and isotopic compositions of the Acropora nobilis skeleton were analyzed at various spatial resolutions to investigate the mechanism by which elements are incorporated into the skeleton. Chemical and isotopic profiles along growth axes of axial and radial corallites did not show seasonal variation, with the exception of the δ18O profile of the axial corallite. Detailed observations of the skeletal structure revealed that the skeletal density increased with distance from the tip because secondarily precipitated aragonite (here called the “infilling” skeleton) filled pore spaces in the “framework” skeleton. Microscale element analyses revealed that main part of the infilling skeleton had lower Mg/Ca and higher Sr/Ca and U/Ca than the framework skeleton. At microscale, Sr/Ca and U/Ca were positively correlated with each other, and negatively correlated with Mg/Ca but only weakly. The results showed that the infilling skeleton differed significantly from the adjacent framework skeleton in terms of not only formation chronology but also chemical composition, and that the bulk composition was influenced by the infilling/framework skeletal ratio. In order to use the Acropora skeleton as a paleoclimate archive, the relationship between environmental factors and the chemical composition of each skeletal component needs to be established.  相似文献   
90.
华南地区是我国重要的金属矿产资源产地,除了发育大量的钨锡钼铋和稀土等金属矿产外,还有铜金矿床分布。本文通过对华南地区29个典型CuMoWSn矿床的时空分布及其与之有关的花岗质岩体的侵位年龄分析,探讨了与不同成矿类型有关的花岗质岩石的地球化学特征。本文认为华南地区10个典型的与Cu有关的矿床主要发生在180~170Ma、160~150Ma以及105~90Ma三个时期,而10个钨矿床主要集中于170~130Ma;4个WSn矿床集中于170~130Ma和120~110Ma;而5个Sn矿床则发育于170~150Ma、130~110Ma以及100~90Ma三个时期。Cu矿床主要与同熔型花岗岩有关,而Mo、WSn既与同熔型花岗岩有关,又与改造型花岗岩有关。在岩石地球化学上,与Cu(Mo)WSn成矿作用有关的花岗质岩石也表现出不同的地球化学特点,如,从Cu(Mo)矿床到WSn矿床SiO2含量有逐渐增大、氧化性逐渐降低、还原性逐渐增加以及分异演化程度有逐渐增高的趋势。与Cu(Mo)Au矿床有关的花岗质岩石具有较低的SiO2(60.3%~68.1%),氧化性较高(Fe2O3/FeO=0.31~1.81),分异演化程度较低(Rb/Sr=0.05~3.3)的特点;与Cu(Pb)(Zn)矿床有关的花岗质岩石具有相对较高的SiO2(73.3%~75.2%),氧化性稍高(Fe2O3/FeO=0.68~1.74),分异程度稍低(Rb/Sr=10.8~57.8)的特点;而与Mo矿床有关的花岗质岩石具有较宽的SiO2(67.3%~76.2%)变化范围,氧化性稍低(Fe2O3/FeO=0.68~1.74),分异演化程度稍低(Rb/Sr=0.6~9.29);与W矿有关的花岗质岩石的SiO2含量为69.9%~80.1%,还原性稍低(Fe2O3/FeO=0.19~0.76),分异演化程度稍高(Rb/Sr=21.9~61.7);与WSn矿床有关的SiO2为74.8%~78.7%,还原性较低(Fe2O3/FeO=0.08~0.59),分异程度较高(Rb/Sr=10.8~139);与Sn矿床有关的花岗质岩石的SiO2为64.8%~76.9%,还原性高(Fe2O3/FeO=0.01~0.58),分异演化程度高(Rb/Sr=1~530)。在结合华南地区花岗岩类岩石的分布特征以及盆岭构造的特点,本文提出华南地区CuMoWSn矿床的成矿作用是不同时期大洋板块或者洋岭多阶段俯冲结果的新成因模型,即早侏罗世休眠的FarallonIzanagi洋岭俯冲导致早—中侏罗世Cu成矿作用;中—晚侏罗世活动的FarallonIzanagi洋岭和转换断层俯冲是中晚侏罗世Cu(Mo)(W)成矿作用以及多阶段WSn成矿作用的触发动力,而白垩纪Izanagi大洋板块俯冲则是白垩纪斑岩型CuWSn成矿作用的诱因。该模型的提出较好地解释了华南中生代大规模岩石圈拆沉—减薄—伸展的机制及其大规模成矿作用的动力。  相似文献   
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