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91.
    
The application of trichloroacetic acid (TCA) as a shell extractant for preparation of soft body parts with reference to tissue metal concentrations (Cd, Cu, Pb, Zn) in shellfish has been evaluated on the example of the mud snail Hydrobia ulvae, a small marine prosobranch densely present in rocky and soft-bottom habitats of the eastern Atlantic. A solution of 0.1 M TCA was tested on individuals treated according to two different protocols: (1) thawed after freezing (\"non-dried\") and (2) thawed and air-dried to a constant weight (\"dried\"). Two points were investigated in detail to improve the method: individual soft tissue dry weight and tissue metal concentration following a standard digestion method. In both instances, the results were compared with those from manually dissected snails. Conditions for total shell decalcification of 60 individuals (3-4 mm long) were 5.5 h in 20 ml of 0.1 M TCA.No differences in individual soft tissue weight were observed between the treatments, indicating good efficiency of the TCA extraction with respect to weight of soft body parts. In contrast, tissue metal concentrations varied among treatments. The TCA extraction of the dried animals had a good recovery for Cd, most likely due to the lower solubility of Cd vital cellular components (proteins and mineral concretions) from the dried tissue. Satisfactory recoveries of the tissue concentrations of Cu and Pb were obtained for the non-dried individuals. This might be related to the specific distribution of metals in the organism (namely in the digestive glands and gonads) and their different chemical reactivity with TCA after the tissue was dried. Limited susceptibility of Zn-bearing protein bindings to complexing with TCA also accounts for significantly lower concentrations of Zn in the mud snail's soft tissue that was extracted. The 0.1 M TCA solution is therefore recommended for extraction of the shells of Hydrobia ulvae for tissue determination of Cd, Cu and Pb; however the treatment protocol does affect metal recovery and thus a consistent procedure should be followed.The extracted metals from the soft tissues and shells of the mud snails (on the basis of both metal concentrations and contents) were ranked in order of increasing contribution of soft body parts to the total (shell+tissue): Pb相似文献   
92.
Ground pressure observations made at Macao (22N, 113E) from 1953 to 1991 are analyzed and compared with the stratospheric quasi-biennial oscillation (QBO) data obtained during the same interval. The periods of the two phenomena and their time evolution are found to be close to each other. Furthermore, the time series of the stratospheric winds and the S2(p) QBO signature are highly correlated, thus confirming earlier analysis. On this basis, pressure measurements obtained at Batavia (now Djakarta: 6S, 107E) from 1870 to 1944 are used to trace back the QBO phenomenon before the advent of systematic stratospheric balloon measurements. The inferred period, which varies between 25 and 32 months, suggests that the QBO has been present in the atmosphere at least since 1870.  相似文献   
93.
    
We present the results of a detailed petrological study of a sparsely phyric basalt (MAPCO CH98-DR11) dredged along the Mid-Atlantic Ridge (30°41′N). The sample contains microphenocrysts of olivine that display four different rapid-growth morphologies. Comparison of these morphologies with those obtained in dynamic crystallization experiments allows us to constrain the thermal history of the sample. The dendritic morphology (swallowtail, chain and lattice olivine) is directly related to the final quenching during magma–seawater interaction. In contrast, the three other morphologies, namely the complex polyhedral crystal, the closed hopper and the complex swallowtail morphology result from several cycles of cooling–heating (corresponding to a maximum degree of undercooling of 20–25°C) during crystal growth. These thermal variations occurred before eruption and are interpreted to be the result of turbulent convection in a small magmatic body beneath the ridge. The results suggest that the Mid-Atlantic Ridge is underlain by a mush zone that releases batches of liquid during tectonic segregation. Aphyric basalts are emitted during eruptions controlled by the tectonic activity, whereas phyric basalts correspond to small fractions of magma from the mush zone mobilized by reinjections of primitive magmas.  相似文献   
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Radiocarbon measurements performed on seawater samples by means of accelerator mass spectrometry (AMS) enable to reduce by a factor of 2000 the water sample size needed for the14C measurements. Therefore no chemical treatment on board the oceanographic vessel is required. Seventy-four AMS14C determinations on samples collected in the tropical-equatorial Indian Ocean during the second leg of the INDIGO program (1986) are presented and compared with the β-counting results obtained during the same campaign and the GEOSECS program (1978). A pronounced reduction of the equatorial14C deficit suggests that substantial amounts of bomb-14C are associated with the westward flowing Pacific water which enters the Indian Ocean via passages through the Indonesia archipelago and/or to meridional mixing with14C-rich water of the southern subtropical gyre.  相似文献   
96.
    
The neodymium-strontium isotopic correlation observed in most of the Earth mantle materials is evaluated by means of direct modelling. Several geochemical models are quantitatively developed to explain the observations. The main results of this modelling are that such a correlation is not geochemically trivial and that it corresponds to specific conditions in chemical fractionation. These specific conditions seem to be satisfied by solid-liquid partitioning in magmatic conditions. The discussion of the experimental data supports a continuous convecting-magmatic fractionation model for a large proportion of the mantle.  相似文献   
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99.
The study of glass inclusions inside mantle minerals provides direct information about the chemistry of naturally occurring mantle-derived melts and the fine-scale complexity of the melting process responsible for their genesis. Minerals in a spinel lherzolite nodule from Grande Comore island contain glass inclusions which, after homogenization by heating, exhibit a continuous suite of chemical compositions clearly distinct from that of the host basanitic lava. The compositions range from silicic, with nepheline–olivine normative, 64 wt% SiO2 and 11 wt% alkali oxides, to almost basaltic, with quartz normative, 50 wt% SiO2 and 1–2 wt% alkali oxides. Within a single mineral phase, olivine, the inferred primary melt composition varies from 54 to 64 wt% SiO2 for MgO content ranging from 8 to 0.8 wt%. An experimental study of the glass and fluid inclusions indicates that trapped melts represent liquids that are in equilibrium with their host phases at moderate temperature and pressure (T≈1230°C and P≈1.0 Gpa for melts trapped in olivine). Quantitative modelling of the compositional trends defined in the suite shows that all of the glasses are part of a cogenetic set of melts formed by fractional melting of spinel lherzolite, with F varying between 0.2 and 5%. The initial highly silicic, alkali-rich melts preserved in Mg-rich olivine become richer in FeO, MgO, CaO and Cr2O3 and poorer in SiO2, K2O, Na2O, Al2O3 and Cl with increasing melt fractions, evolving toward the basaltic melts found in clinopyroxene. These results confirm the connection between glass inclusions inside mantle minerals and partial mantle melts, and indicate that primary melts with SiO2 >60 wt%, alkali oxides >11%, FeO <1 wt% and MgO <1 wt% are generated during incipient melting of spinel peridotite. The composition of the primary melts is inferred to be dependent on pressure, and to reflect both the speciation of dissolved CO2 and the effect of alkali oxides on the silica activity coefficient in the melt. At pressures around 1 GPa, low-degree melts are characterized by alkali and silica-rich compositions, with a limited effect of dissolved CO2 and a decreased silica activity coefficient caused by the presence of alkali oxides, whereas at higher pressures alkali oxides form complexes with carbonates and, consequently, alkali-rich silica-poor melts will be generated.  相似文献   
100.
    
Linear Alkylbenzene Sulfonates (LAS) are ubiquitous surfactants. Traces can be found in coastal environments. Sorption and toxicity of C12-LAS congeners were studied in controlled conditions (2-3500 μg C12LAS/L) in five marine phytoplanktonic species, using standardized methods. IC50 values ranged from 0.5 to 2 mg LAS/L. Sorption of 14C12-6 LAS isomer was measured at environmentally relevant trace levels (4 μg/L) using liquid scintillation counting. Steady-state sorption on algae was reached within 5 h in the order dinoflagellate > diatoms > green algae. The sorption data, fitted a L-type Freundlich isotherm, indicating saturation. Desorption was rapid but a low LAS fraction was still sorbed after 24 h. Toxic cell concentration was 0.38 ± 0.09 mg/g for the studied species. LAS toxicity results from sorption on biological membranes leading to non-specific disturbance of algal growth. Results indicate that LAS concentrations in coastal environments do not represent a risk for these organisms.  相似文献   
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