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111.
Boron samples from 40 fumarolic condensates from volcanoes in the Ryukyu arc (Satsuma Iwo-jima and Shiratori Iwo-yama) and the North-east Japan arc (Usu-shinzan, Showa-shinzan, Esan and Issaikyo-yama) all have 11B10B ratios close to 4.07. Higher values, from 4.09 to 4.13, were only observed in condensates from volcanoes in the southernmost end of the North-east Japan arc (Nasu-dake), the northern part of the Izu-Bonin arc (Hakone), and the North Mariana arc (Ogasawara Iwo-jima). These higher values suggest geological interaction of the magmas with sea-water enriched in 11B.  相似文献   
112.
In Funka Bay of Hokkaido, Japan, seawater, suspended matter and settling matter were collected once every month in the summer of 1974. These samples were analyzed for234Th, a short-lived daughter of dissolved238U. A pronounced disequilibrium between234Th and238U, and a highly variable concentration of234Th were found. Positive correlation, however, exist among the deficiency of234Th relative to238U in seawater, the concentration of particulate234Th, the fraction of particulate234Th to total234Th in seawater, the total dry weight of suspended matter, and the primary productivity during the month previous to sampling. The specific activity of234Th for the settling particles (620 ± 170 dpm/g) was nearly equal to that for suspended particles (720 ± 600 dpm/g) but much greater than that for plankton (47 ± 24 dpm/g). These facts suggest that suspended particles are somehow closely related to the removal of heavy metals from seawater, in spite of the negligibly small settling flux of suspended matter. The residence time of thorium in Funka Bay (mean depth: 60 m) is found to be about 60 days, which is nearly equal to those of210Pb and210Po.  相似文献   
113.
Bulletin of Volcanology -  相似文献   
114.
Micro‐X‐ray fluorescence scanning spectroscopy of marine and lake sedimentary sequences can provide detailed palaeoenvironmental records through element intensity proxy data. However, problems with the effects of interstitial pore water on the micro‐X‐ray fluorescence intensities have been pointed out. This is because the X‐ray fluorescence intensities are measured directly at the surfaces of split wet sediment core samples. This study developed a new method for correcting X‐ray fluorescence data to compensate for the effects of pore water using a scanning X‐ray analytical microscope. This involved simultaneous use of micro‐X‐ray fluorescence scanning spectroscopy and an X‐ray transmission detector. To evaluate the interstitial pore water content from the X‐ray transmission intensities, a fine‐grained sediment core retrieved from Lake Baikal (VER99‐G12) was used to prepare resin‐embedded samples with smooth surfaces and uniform thickness. Simple linear regression between the linear absorption coefficients of the samples and their porosity, based on the Lambert–Beer law, enabled calculation of the interstitial pore spaces and their resin content with high reproducibility. The X‐ray fluorescence intensities of resin‐embedded samples were reduced compared with those of dry sediment samples because of: (i) the X‐ray fluorescence absorption of resin within sediment; and (ii) the sediment dilution effects by resin. An improved micro‐X‐ray fluorescence correction equation based on X‐ray fluorescence emission theory considers the instrument's sensitivity to each element, which provides a reasonable explanation of these two effects. The resin‐corrected X‐ray fluorescence intensity was then successfully converted to elemental concentrations using simple linear regression between the data from micro‐X‐ray fluorescence scanning spectroscopy and from the conventional analyzer. In particular, the calculated concentration of SiO2 over the depth of the core, reflecting diatom/biogenic silica concentration, was significantly changed by the calibrations, from a progressively decreasing trend to an increasing trend towards the top of the core.  相似文献   
115.
Geochemistry of a sediment core from Lake Hovsgol, northwest Mongolia provides a continuous, 27-kyr history of the response of the lake and the surrounding catchment to climate change. Principle component (PC) analysis of 19 major and trace elements, total inorganic carbon (TIC), and total organic carbon (TOC) in the bulk sediment samples revealed that the 21 chemical components can be grouped into four assemblages—group-1: Na, Mg, Ca, Sr, and TIC, hosted in carbonate minerals (calcite, dolomite, and magnesian calcite); group-2: Ni, Cu, and Zn, recognized as biophilic trace metals, and TOC; group-3: Al, K, Ti, V, Fe, Rb, Cs, Ba, and Pb, composed of rock-forming minerals; and group-4: Cr, Mn, and As, sensitive to the redox condition of the sediment. The four element assemblages originated from three relevant processes. Group-1 and group-2 components are authigenic products and comprise the end member on the PC-1 score, whose variation reflects changes in the water volume, i.e. the balance between precipitation and evaporation (P/E). Group-3 components from detrital materials of the catchment contribute to the PC-2 score, whose variability indicates erosion/weathering intensity in the drainage basin, which might be controlled by the amount of vegetation cover associated with moisture change. The group-4 components of redox-sensitive elements contribute to the PC-3 score and are not an end member because of their small amount. The first two PC scores suggest a sequential record of paleo-moisture evolution in central Asia. The P/E balance in the Lake Hovsgol region, inferred from the PC-1 score, gradually increased during the glacial/interglacial transition. This resembles climate change of the North Atlantic region on the glacial–interglacial scale, but does not reflect the abrupt climate shifts such as the warm Bølling-Allerød and the cold Younger Dryas of the North Atlantic on the millennial scale. A periodic variation of ~8.7 kyr was observed in the PC-2 score profile of detrital input to Lake Hovsgol over the last glacial and Holocene. The decrease in detrital input coincided with the copious supply of moisture from the Asian monsoon regime and the North Atlantic westerly winds to the Baikal drainage basin, which includes Lake Hovsgol. Our geochemical records from Lake Hovsgol demonstrate that the climate system of interior continental Asia was strongly influenced by change on both Milankovitch and sub-Milankovitch scales.  相似文献   
116.
The response of a viscoelastic Earth to the melting of the Late Pleistocene ice sheets has been the subject of a number of investigations employing PREM. In PREM, a non-adiabatic density gradient (NADG) exists in the upper mantle, and to understand the implications of this model it is thus important to examine the effects of this NADG on the Earth's response to surface loads. This paper is based on the assumption that the contribution to the depth dependence of the density that is not due to self-compression is due to compositional change. This contribution is referred to as 'non-adiabatic'. We evaluate the effects of a non-adiabatic density jump (NADJ) for the 670  km discontinuity and the NADG in the upper mantle by adopting a compressible earth model with both a compositional density gradient and a density jump. Numerical calculations based on these models indicate that the magnitude of the Earth's response associated with the NADG is much smaller than that associated with the NADJ at 670  km depth. It is also confirmed that the higher modes associated with the NADJ and the NADG are much more sensitive to the existence of an elastic lithosphere than the fundamental modes associated with the density jumps at the surface and core–mantle boundary.  相似文献   
117.
In order to examine the transportation and deposition mechanisms of Hg, we investigated the ore and hydrothermal alteration minerals and solid organic matters from Itomuka mercury mine located in the eastern part of central Hokkaido. In addition to the ore minerals, native mercury and cinnabar, quartz, marcasite, alunite, kaolinite, and minor amounts of pyrite and smectite were identified in the Hg ore by powder X‐ray diffraction (XRD) analysis. This mineral assemblage of acid sulfate alteration was likely developed under the conditions of low temperature (≤100°C) and low pH (≤2) in the steam‐heated environment. The H2SO4 was produced above the water table by the oxidation of H2S separated from deep, near‐neutral fluids by boiling. The dominance of native mercury over cinnabar in Hg ore indicates that the greater part of mineralized Hg was transported as Hg0 in aqueous solution and vapor with low sulfur fugacity. The solid organic matters found in the Hg ore were analyzed with SEM‐EDS, micro‐XRD, and micro‐Fourier transform infrared (FTIR) spectroscopy, and these results suggest that the organic matters contributed to keeping the low fO2 of the Hg‐bearing fluid and transportation of Hg as Hg0 in S‐poor condition. Because the solubility of Hg in acidic fluid is low, neutral to alkaline fluid seems to have leached Hg from the basement sedimentary rocks of Hidaka Group which also supplied the organic matters to the fluid. The oxidation and cooling of Hg‐bearing solution and vapor triggered the deposition of liquid Hg as a primary phase.  相似文献   
118.
The Ocean Color and Temperature Scanner (OCTS) aboard the Advanced Earth Observing Satellite (ADEOS) can observe ocean color and sea surface temperature (SST) simultaneously. This paper explains the algorithm for the OCTS SST product in the NASDA OCTS mission. In the development of the latest, third version (V3) algorithm, the OCTS match-up dataset plays an important role, especially when the coefficients required in the MCSST equation are derived and the equation form is adjusted. As a result of the validation using the OCTS match-up dataset, the algorithm has improved the root mean square (rms) error of the OCTS SST up to 0.698°C although some problems remain in the match-up dataset used in the present study.  相似文献   
119.
The ‘International Intercomparison Exercise of fCO2 Systems’ was carried out in 1996 during the R/V Meteor Cruise 36/1 from Bermuda/UK to Gran Canaria/Spain. Nine groups from six countries (Australia, Denmark, France, Germany, Japan, USA) participated in this exercise, bringing together 15 participants with seven underway fugacity of carbon dioxide (fCO2) systems, one discrete fCO2 system, and two underway pH systems, as well as systems for discrete measurement of total alkalinity and total dissolved inorganic carbon. Here, we compare surface seawater fCO2 measured synchronously by all participating instruments. A common infrastructure (seawater and calibration gas supply), different quality checks (performance of calibration procedures for CO2, temperature measurements) and a common procedure for calculation of final fCO2 were provided to reduce the largest possible amount of controllable sources of error. The results show that under such conditions underway measurements of the fCO2 in surface seawater and overlying air can be made to a high degree of agreement (±1 μatm) with a variety of possible equilibrator and system designs. Also, discrete fCO2 measurements can be made in good agreement (±3 μatm) with underway fCO2 data sets. However, even well-designed systems, which are operated without any obvious sign of malfunction, can show significant differences of the order of 10 μatm. Based on our results, no “best choice” for the type of the equilibrator nor specifics on its dimensions and flow rates of seawater and air can be made in regard to the achievable accuracy of the fCO2 system. Measurements of equilibrator temperature do not seem to be made with the required accuracy resulting in significant errors in fCO2 results. Calculation of fCO2 from high-quality total dissolved inorganic carbon (CT) and total alkalinity (AT) measurements does not yield results comparable in accuracy and precision to fCO2 measurements.  相似文献   
120.
High-resolution geochemical, isotope and elemental data from core PC23A in the northern margin of the Aleutian Basin (Bering Sea) were used to reconstruct distinct paleoceanographic features of the last deglaciation (pre-Boreal[PB], Bølling-Allerød[BA], Younger Dryas[YD]). The PB and BA intervals are characterized by increased siliceous (diatom) and calcareous (coccolithophores and foraminifers) productivity represented by high biogenic opal and CaCO3 contents, respectively. The enhanced productivity can plausibly be attributed to an elevated sea-surface nutrient supply from increased melt-water input and enhanced Alaskan Stream injection under warm, restricted sea-ice conditions. High Corg/N ratios and low δ13C values of sediment organic matter during the PB and BA intervals reflect the contribution of terrestrial organic matters. The PB and BA intervals were also identified by laminated sediment layers of core PC23A, characterized by high Mo/Al and Cd/Al ratios, indicating that the bottom water condition remained anoxic. High δ15N values during the same period were attributed mainly to the increased nutrient utilization and subsequent denitrification of seawater nitrate. Part of high δ15N values may also be due to incorporation of inorganic nitrogen in the clay minerals. It is worthy of note that high total organic carbon (TOC) deposition occurred approximately 3,000 years before onset of the last deglaciation. Simultaneous high Corg/N ratios and low δ13C values clearly suggest that the high TOC content should be related to terrestrial organic carbon input. Low δ15N values during the high TOC interval also confirm the contribution of terrigenous organic matter. Although abundant calcareous phytoplankton production under cold, nutrient-poor conditions represented by Baex data was reported for high TOC deposition preceding the last deglaciation in an earlier study of the Okhotsk Sea, the main reason for the enhanced TOC deposition in the Bering Sea is an increased terrigenous input from the submerged continental shelves (Beringia) with a sea-level rise; this is further supported by Al enrichment of bulk sediments during the high TOC deposition.  相似文献   
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