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131.
The effects of food web structure on the quantity and biochemical composition of seston, zooplankton and recently deposited sediment in experimental freshwater mesocosms were examined. Food web structure was manipulated by addition of zooplanktivorous fish. Biochemical characterisations were carried out using lipid biomarkers (sterols, fatty acids, chlorophyll-derived compounds and long-chain alkanediols). Fish addition decreased zooplankton biomass and increased seston biomass and deposited sediment through a trophic cascade. Fish presence strongly influenced the biochemical characteristics of seston and sediment. In contrast, food web structure had a minor impact on the lipid biomarker composition of zooplankton. Although the relative abundance of sterols in the different compartments did not differ strongly between treatments, sterol profiles in seston and sediment depended on food web structure. The predominance of Δ7-sterols in seston and sediment in the fish treatment indicated a major contribution of Chlorophyceae. In contrast, the distribution of sterols in seston and sediment in the fishless treatment, dominated by cholesterol, indicated a major zooplanktonic input. The distribution of fatty acids and the relative abundance of chlorophyll-derived compounds and long-chain alkanediols agreed with the predominant contribution of phytoplankton or zooplankton to seston and sediment in the two treatments. The relative abundance of bacterial biomarkers suggested that the contribution of bacteria was rather low. The high relative abundance of polyunsaturated fatty acids (PUFAs) and the absence of stanols in sediments suggested low microbial reworking of organic matter in the recently accumulated sediments. The trophic cascade, generated by the addition of fish, increased the relative abundance of PUFAs in deposited organic matter, thus enhancing sediment quality and potential degradability.  相似文献   
132.
133.
Summary M?ller's assumptions for the carbon dioxide-water vapor overlap region, which lead to the construction of his radiation chart, are reinvestigated in the light of modern theory. A new radiation chart, taking into account the carbon dioxide-water vapor overlap, is constructed using water vapor and carbon dioxide absorption data as furnished byM?ller andElsasser respectively. The results of the radiative fluxes computed from the new chart are compared with equivalent results using the original M?ller and the revised Elsasser radiation diagrams, as well as with measurements.
Zusammenfassung Die Berechtigung derM?llerschen Annahme zur getrennten Behandlung von Kohlens?ure- und Wasserdampfabsorption zwecks Konstruktion eines atmosph?rischen Strahlungsdiagrammes wird im Lichte der modernen Theorie diskutiert. Ein neues Strahlungspapier wird vorgelegt, das die gleichzeitige Anwesenheit von Kohlens?ure und Wasserdampf im gleichen Spektralbereich berücksichtigt. Dieses beruht auf Wasserdampf- und Kohlens?uredaten, die vonM?ller undElsasser vorgegeben wurden. Nach dem neuen Strahlungsdiagramm berechnete Werte werden mit Me?werten und theoretischen Werten verglichen, die mit dem ursprünglichen M?llerschen und mit dem verbesserten Elsasserschen Strahlungspapier ermittelt wurden.

Résumé Au vu des théories modernes, on discute l'hypothèse formulée parM?ller et sa justification, hypothèse selon laquelle il est nécessaire de traiter séparément l'absorption du dioxyde de carbone et celle de la vapeur d'eau lors de l'établissement d'un diagramme du rayonnement atmosphérique. On propose alors un nouvel abaque qui tient compte de la présence simultanée du dioxyde de carbone et de la vapeur d'eau dans la même région spectrale. Cet abaque s'appuie sur les valeurs données parM?ller et parElsasser, valeurs valables pour ces deux gaz. On compare le résultat de calculs effectués avec ce nouvel abaque à des mesures et à des valeurs théoriques ces dernières étant basées tant sur les travaux originaux deM?ller que sur l'abaque amélioré deElsasser.


With 4 Figures  相似文献   
134.
A Kalman filter-based method combining the energy of both L1 C/A and L2C GPS signals in a combined tracking loop method to enhance performance under adverse conditions is developed. Standard tracking methods and the ionospheric effect on GPS signals are reviewed and compared to a new Kalman filter that simultaneously estimates delay, phase and total electron content by combining L1 C/A and L2C code and phase discriminator outputs. The new filter is tested and compared to standard methods for tracking L1 C/A and L2C using both simulated and real data. The new method is found to have improved sensitivity of 3 dB compared to standard L1 tracking and 4.5 dB compared to standard L2C tracking while at the same time providing an accurate estimate of the total electron content along the signal path.  相似文献   
135.
Using surface charts at 0330GMT, the movement of the monsoon trough during the months June to September 1990 at two fixed longitudes, namely 79°E and 85°E, is studied. The probability distribution of trough position shows that the median, mean and mode occur at progressively more northern latitudes, especially at 85°E, with a pronounced mode that is close to the northern-most limit reached by the trough. A spectral analysis of the fluctuating latitudinal position of the trough is carried out using FFT and the Maximum Entropy Method (MEM). Both methods show significant peaks around 7.5 and 2.6 days, and a less significant one around 40–50 days. The two peaks at the shorter period are more prominent at the eastern longitude. MEM shows an additional peak around 15 days. A study of the weather systems that occurred during the season shows them to have a duration around 3 days and an interval between systems of around 9 days, suggesting a possible correlation with the dominant short periods observed in the spectrum of trough position.  相似文献   
136.
Abstract: The solubility of gold was studied in water and aqueous NaCl (1– 5 m) solutions under oxygen and sulfur buffered conditions between 300–500C at a constant pressure 1 kb. Two buffer assemblages HMP and PPM were used. Analysis of the scatter in measured values in log mAu–mNaCl–T frame fixed linear dependence between log mAu and T at any studied iso‐pleth (mNaCl) in the form of log mAu = a. T(C) + b. Coefficients of the equation were calculated for water and NaCl (1, 3, 5 m) solutions. The maximum solubility characterizes the NaCl‐free system in the presence of HMP. In the case, Au solubility increases from (log mAu) –6. 72 to –5. 04 at 300 and 500C, respectively. In the presence of PPM, maximum of Au solubility was obtained for the 5 mNaCl solution. In a similar manner solubility rises from –6. 54 to –5. 77 at 300 and 500C, accordingly. In studied fO2/fS2 area the behavior of Au solubility testified that: (i) – a composite interaction between chloride and hydrosulfide speciation of gold affects its total solubility; (ii) – in addition of NaCl up to about 1. 5 m the solubility decreases, more pronounced in the presence of HMP; (iii) – the contribution of chloride in total Au solubility is more for PPM despite of lower fO2value, than for HMP. The solubility of platinum was studied in the Pt–Cl–S–H2O system between 300 and 500C, 1 kb. PPM solid buffer controlled oxidation state, pH and sulfur activity of solutions (H2O, 1 mNaCl and 0. 1 mHCl). Under the conditions, PtS precipitated from the solutions with increasing temperature and acidity. The PtS solubility in the 0. 1 mHCl solutions lowers slightly in the range of 300–500C from –5. 30 to –5. 60 (in log mPt) that is typical to the hydrosulfide species. It was deduced that reducing media, regulated by the PPM assemblage, suppress activity of chloride species of Pt. More oxidizing conditions were modeled in runs using mixtures of Mn(II), Mn(III) and Mn(IV) oxides to buffer the aqueous‐chloride solutions between 300 and 500C, 1 kb. It was found that MnO tends to oxidize at T below 400C forming intermediate Mn‐hydroxides (β–MnOOH, Mn (OH)2 and Mn2(OH)3Cl). These phases are metastable and transfer to Mn3O4 with increasing duration. Generation of the Mn‐hydroxides leads to a change of physical‐chemical parameters of the solutions, such as water activity, pH and Eh. The last results in abrupt increase in the noble metals dissolution. At stable existence of only Mn3O4, the solubility of both Pt and Au lowers to equilibrium values. Essential catalysis effect of Pt on intensity and rate of Mn(II) oxidation was found. The dominant role of chloride of Pt and Au was defined under most oxidized conditions, specified by Mn2O3–MnO2 buffer. So at 400C, dissolved Au (log mAu) increases from –4. 40 in water to –1. 00 in 0. 1 mHCl, and ones of Pt (log mPt) from –4. 80 to –2. 90 accordingly. Thus, mixing of hydrosulfide and chloride solutions, as well as transformation of the systems to the stable state act upon total solubility of the noble metals.  相似文献   
137.
In this study, a method is proposed for estimating the uncertainty of a Lagrangian pathway calculated from an undersampled ocean surface velocity field. The primary motivation and application for this method is the differentiation between active and passive movements for sea turtles whose trajectories are observed with satellite telemetry. Synthetic trajectories are launched within a reconstructed surface velocity field and integrated forward in time to produce likely trajectories of an actual turtle or drifter. Uncertainties in both the initial conditions at launch and the velocity field along the trajectory are used to yield an envelope of possible synthetic trajectories for each actual trajectory. The juxtaposition of the actual trajectory with the resulting cloud of synthetic trajectories provides a means to distinguish between active and passive movements of the turtle. The uncertainty estimates provided by this model may lead to improvements in our understanding of where and when turtles are engaged in specific behaviors (i.e. migration vs. foraging)—for which potential management efforts may vary accordingly.  相似文献   
138.
The 2006 western Java tsunami deposited a discontinuous sheet of sand up to 20 cm thick, flooded coastal southern Java to a depth of at least 8 m and inundated up to 1 km inland. In most places the primarily heavy mineral sand sheet is normally graded, and in some it contains complex internal stratigraphy. Structures within the sand sheet probably record the passage of up to two individual waves, a point noted in eyewitness accounts. We studied the 2006 tsunami deposits in detail along a flow parallel transect about 750 m long, 15 km east of Cilacap. The tsunami deposit first becomes discernable from the underlying sediment 70 m from the shoreline. From 75 to 300 m inland the deposit has been laid down in rice paddies, and maintains a thickness of 10–20 cm. Landward of 300 m the deposit thins dramatically, reaching 1 mm by 450 m inland. From 450 m to the edge of deposition (around 700 m inland) the deposit remains <1 mm thick. Deposition generally attended inundation—along the transect, the tsunami deposited sand to within about 40 m of the inundation limit. The thicker part of the deposit contains primarily sand indistinguishable from that found on the beach 3 weeks after the event, but after about 450 m (and roughly coinciding with the decrease in thickness) the tsunami sediment shifts to become more like the underlying paddy soil than the beach sand. Grain sizes within the deposit tend to fine upward and landward, although overall upward fining takes place in two discrete pulses, with an initial section of inverse grading followed by a section of normal grading. The two inversely graded sections are also density graded, with denser grains at the base, and less dense grains at the top. The two normally graded sections show no trends in density. The inversely graded sections show high density sediment to the base and become less dense upward and represents traction carpet flows at the base of the tsunami. These are suggestive of high shear rates in the flow. Because of the grain sorting in the traction carpet, the landward-fining trends usually seen in tsunami deposits are masked, although lateral changes of mean sediment grain size along the transect do show overall landward fining, with more variation as the deposit tapers off. The deposit is also thicker in the more seaward portions than would be produced by tsunamis lacking traction carpets.  相似文献   
139.
The Golden Pride gold deposit (∼3 Moz) is located in the central part of the Nzega Greenstone Belt at the southern margin of the Lake Victoria Goldfields in Tanzania. It represents an inferred Late Archaean, orogenic gold deposit and is hosted in intensely deformed meta-sedimentary rocks in the hanging wall of the approximately E–W striking Golden Pride Shear Zone. The hanging-wall sequence also includes felsic (quartz porphyritic) to mafic (lamprophyric) intrusions, as well as banded iron formations. Hydrothermal alteration phases associated with mineralisation are dominated by sericite and chlorite. Two main ore types can be distinguished, chlorite and silica ore, both occupying dilational sites and structural intersections in the hanging wall of the main shear zone. Sulphide minerals in both ore types include pyrrhotite, arsenopyrite, pyrite and accessory sphalerite, galena, sulphosalts and Ni–Co–Bi sulphides. Gold and tellurides are late in the paragenetic sequence and associated with a secondary phase of pyrrhotite deposition. Sulphur isotope compositions range from −6 to 7 per mil and are interpreted to reflect contributions from two distinct sources to the mineralising fluids in the Golden Pride gold deposit. A redox change, potentially induced by the intrusion of mafic melts, together with structural elements in the hanging wall of the Golden Pride Shear Zone, are interpreted to be the main controls on gold mineralisation in this deposit.  相似文献   
140.
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