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91.
The spectrophotometric measurements of chloro complexes of lead in aqueous HCl, NaCl, MgCl2 and CaCl2 solutions at 25°C have been analyzed using Pitzer's specific interaction equations. Parameters for activity coefficients of the complexes PbCl+, PbCl20 and PbCl3? have been determined for the various media. Values of K1 = 30.0 ± 0.6, K2 = 106.7 ± 2.1 and K3 = 73.0 ± 1.5 were obtained for the cumulative formation constants. [Pb2+ + nCl? → PbCln2?n)]. These values are in reasonable agreement with literature data. The Pitzer parameters for the PbCl ion pairs in various media were used to calculate the speciation of Pb2+ in an artificial seawater solution.  相似文献   
92.
Ladakh (India) provides a complete geological section through the northwestern part of the Himalayas from Kashmir to Tibet. Within this section the magmatic, metamorphic and geotectonic evolution of the northern Himalayan orogeny has been studied using petrographic, geochemical and isotope analytical techniques.The beginning of the Himalayan cycle was marked by large basaltic extrusions (Panjal Trap) of Permian to Lower Triassic age at the “northern” margin of the Gondwana continent (Indian Shield). These continental type tholeiitic basalts were followed by a more alkaline volcanism within the Triassic to Jurassic Lamayuru unit of the Gondwana continental margin.Lower Jurassic to Cretaceous oceanic crust and sediments (ophiolitic mélange s.s.) accompany the Triassic to Cretaceous flysch deposits within the Indus-Tsangpo suture zone, the major structural divide between the Indian Shield (High Himalaya) and the Tibetan Platform. So far, no relic of Paleozoic oceanic crust has been found.Subduction of the Tethyan oceanic crust during Upper Jurassic and Cretaceous time produced an island arc represented by tholeiitic and calc-alkaline volcanic rock series (Dras volcanics) and related intrusives accompanied by volcaniclastic flysch deposits towards the Tibetan continental margin.Subsequent to the subduction of oceanic crust, large volumes of calc-alkaline plutons (Trans-Himalayan or Kangdese plutons) intruded the Tibetan continental margin over a distance of 2000 km and partly the Dras island arc in the Ladakh region.The collision of the Indian Shield and Tibetan Platform started during the middle to upper Eocene and caused large-scale, still active intracrustal thrusting as well as the piling up of the Himalayan nappes. The tectonically highest of these nappes is built up of oceanic crust and huge slices of peridotitic oceanic mantle (Spongtang klippe).In the High Himalayas the tectonic activity was accompanied and outlasted by a Barrovian-type metamorphism that affected Triassic sediments of the Kashmir-Nun-Kun synclinorium up to kyanite/staurolite grade and the deeper-seated units up to sillimanite grade. Cooling ages of micas are around 20 m.y. (muscovite) and 13 m.y. (biotite). Towards the Indus-Tsangpo suture zone metamorphism decreases with no obvious discontinuity through greenschist, prehnite-pumpellyite to zeolite grade. Remnants of possibly an Eo-Himalayan blueschist metamorphism have been found within thrust zones accompanying ophiolitic mélange in the suture zone.  相似文献   
93.
Any conductive sulphide ore body can generate electrical ore potentials and this can be regarded as a geobattery, with an upper positive cathode and a lower negative anode. Two mechanisms which can occur simultaneously and which appear to explain these potentials are the oxygen concentration cell (OCC) and the sulphide galvanic cell (SGC). When there is a difference of O2 concentration between the cathode and anode, the OCC operates by contributing oxygen to the anode, and ceases when the difference is diminished. However, gradients of pH, temperature or pressure can keep the cell operating. In the SGC the sulphides dissolve at the anode (producing metal ions, sulphur and electrons), while at the cathode, either sulphides dissolve producing metal and sulphur ions, or reaction is as in the OCC. The ore potential measured in the field is the sum of the oxygen concentration cell and at times locally dominant sulphide galvanic cells.  相似文献   
94.
The “anomalous” layer in the lowermost mantle, identified as D″ in the notation of K.E. Bullen, appears in the PREM Earth model as a 150 km-thick zone in which the gradient of incompressibility with pressure, dKdP, is almost 1.6, instead of 3.2 as in the overlying mantle. Since PREM shows no accompanying change in density or density gradient, we identify D″ as a thermal boundary layer and not as a chemically distinct zone. The anomaly in dKdP is related to the temperature gradient by the temperature dependence of Ks, for which we present a thermodynamic identity in terms of accessible quantities. This gives the numerical result (?Ks/?T)P=?1.6×107 Pa K?1 for D″ material. The corresponding temperature increment over the D″ range is 840 K. Such a layer cannot be a static feature, but must be maintained by a downward motion of the lower mantle toward the core-mantle boundary with a strong horizontal flow near the base of D″. Assuming a core heat flux of 1.6 × 1012 W, the downward speed is 0.07 mm y?1 and the temperature profile in D″, scaled to match PREM data, is approximately exponential with a scale height of 73 km. The inferred thermal conductivity is 1.2 W m?1 K?1. Using these values we develop a new analytical model of D″ which is dynamically and thermally consistent. In this model, the lower-mantle material is heated and softened as it moves down into D″ where the strong temperature dependence of viscosity concentrates the horizontal flow in a layer ~ 12 km thick and similarly ensures its removal via narrow plumes.  相似文献   
95.
96.
Adsorption and Desorption of Phosphate on Calcite and Aragonite in Seawater   总被引:3,自引:0,他引:3  
The adsorption and desorption of phosphate on calcite and aragonite were investigated as a function of temperature (5–45 °C)and salinity (0–40) in seawater pre-equilibrated with CaCO3. An increase in temperature increased the equilibrium adsorption; whereas an increase in salinity decreased the adsorption. Adsorption measurements made in NaCl were lower than the results in seawater. The higher values in seawater were due to the presence of Mg2+ and Ca2+ ions. The increase was 5 times greater for Ca2+ than Mg2+. The effects ofCa2+ and Mg2+ are diminished with the addition of SO4 2- apparently due to the formation of MgSO4 and CaSO4 complexes in solution and/or SO4 2- adsorption on the surface of CaCO3. The adsorbed Ca2+ and Mg2+ on CaCO3 (at carbonate sites) may act as bridges to PO4 3- ions. The bridging effect of Ca2+is greater than Mg2+ apparently due to the stronger interactions of Ca2+ with PO4 3-.The apparent effect of salinity on the adsorption of PO4 was largely due to changes in the concentration of HCO3 - in the solutions. An increase in the concentration of HCO3 - caused the adsorption of phosphate to decrease, especially at low salinities. The adsorption at the same level of HCO3 - (2 mM) was nearly independent of salinity. All of the adsorption measurements were modeled empirically using a Langmuir-type adsorption isotherm[ [PO4]ad = KmCm[PO4]T/(1 +Km [PO4]T) , ]where [PO4]ad and [PO4]T are the adsorbed and total dissolved phosphate concentrations, respectively. The values of Cm (the maximum monolayer adsorption capacity, (mol/g) and Km (the adsorption equilibrium constant, g/(mol) over the entire temperature (t, °C) and salinity (S) range were fitted to[ Cm = 17.067 + 0.1707t - 0.4693S + 0.0082S2 ( = 0.7) ][ ln Km = - 2.412 + 0.0165t - 0.0004St - 0.0008S2 ( = 0.1) ]These empirical equations reproduce all of our measurements of[PO4]ad up to 14 mol/g and within ±0.7 mol/g.The kinetic data showed that the phosphate uptake on carbonate minerals appears to be a multi-step process. Both the adsorption and desorption were quite fast in the first stage (less than 30 min) followed by a much slower process (lasting more than 1 week). Our results indicate that within 24 hours aragonite has a higher sorption capacity than calcite. The differences between calcite and aragonite become smaller with time. Consequently, the mineral composition of the sediments may affect the short-term phosphate adsorption and desorption on calcium carbonate. Up to 80 % of the adsorbed phosphate is released from calcium carbonate over one day. The amount of PO4 left on the CaCO3 is close to the equilibrium adsorption. The release of PO4 from calcite is faster than from aragonite. Measurements with Florida Bay sediments produced results between those for calcite and aragonite. Our results indicate that the calcium carbonate can be both a sink and source of phosphate in natural waters.  相似文献   
97.
The time-dependence of earthquake occurrence is mostly ignored in standard seismic hazard assessment even though earthquake clustering is well known. In this work, we attempt to quantify the impact of more realistic dynamics on the seismic hazard estimations. We include the time and space dependences between earthquakes into the hazard analysis via Monte Carlo simulations. Our target region is the Lower Rhine Embayment, a low seismicity area in Germany. Including aftershock sequences by using the epidemic type aftershock-sequence (ETAS) model, we find that on average the hypothesis of uncorrelated random earthquake activity underestimates the hazard by 5–10 per cent. Furthermore, we show that aftershock activity of past large earthquakes can locally increase the hazard even centuries later. We also analyse the impact of the so-called long-term behaviour, assuming a quasi-periodic occurrence of main events on a major fault in that region. We found that a significant impact on hazard is only expected for the special case of a very regular recurrence of the main shocks.  相似文献   
98.
    
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99.
Future mineral exploration within eastern Australia will be enhanced by resolving the tectonic evolution of the Lachlan Orogen to establish the spatial and temporal terrane distribution of the various mineral deposits. The Lachlan Orogen, from north-eastern Tasmania through to central and eastern New South Wales, is host to a number of major mineral deposit styles—including orogenic gold (e.g. Stawell, Ballarat, Bendigo), volcanic-hosted massive sulphide (e.g. Woodlawn, Currawong), sediment-hosted Cu–Au (e.g. Cobar Basin deposits), porphyry Au–Cu (e.g. Cadia, Parkes, Cowal) and granite-related Sn (e.g. Ardlethan, Beechworth). Each of these mineral deposit styles is a sensitive and diagnostic indicator of the prevalent tectonic environment during their formation. In this review, we briefly summarise the deposit- to large-scale factors that define the diverse metallogenic evolution of the Lachlan Orogen. This overview is intended to “set the scene” for subsequent specialist papers published in this thematic issue on the metallogeny and tectonics of the Lachlan Orogen in south-east Australia.  相似文献   
100.
In a recent paper, Nof et al. (J Paleolimnol 35:417–439, 2006) suggest a physical mechanism which could account for the formation of ice on Lake Kinneret (Sea of Galilee) in northern Israel. Based on the sea surface temperature record of sediment cores from the Mediterranean Sea the authors argue that centennial-scale cold events had the potential to trigger local ‘springs ice’ formation on the lake in the past. Here, we demonstrate that a closer inspection of the paleoceanographic record in combination with correlation and regression analyses of meteorological data provides no evidence for such cold events in the lake region during the last 10,000 years. Thus, the formation of ‘springs ice’ on Lake Kinneret was unlikely at least since the beginning of the Neolithic.  相似文献   
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