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101.
This study presents a new experimental approach for determining H2O solubility in basaltic melt at upper mantle conditions. Traditional solubility experiments are limited to pressures of ~600 MPa or less because it is difficult to reliably quench silicate melts containing greater than ~10 wt% dissolved H2O. To overcome this limitation, our approach relies on the use of secondary ion mass spectrometry to measure the concentration of H dissolved in olivine and on using the measured H in olivine as a proxy for the concentration of H2O in the co-existing basaltic melt. The solubility of H2O in the melt is determined by performing a series of experiments at a single pressure and temperature with increasing amounts of liquid H2O added to each charge. The point at which the concentration of H in the olivine first becomes independent of the amount of initial H2O content of the charge (added + adsorbed H2O) indicates its solubility in the melt. Experiments were conducted by packing basalt powder into a capsule fabricated from San Carlos olivine, which was then pressure-sealed inside a Ni outer capsule. Our experimental results indicate that at 1000 MPa and 1200 °C, the solubility of H2O in basaltic melt is 20.6 ± 0.9 wt% (2 × standard deviation). This concentration is considerably higher than predicted by most solubility models but defines a linear relationship between H2O fugacity and the square of molar H2O solubility when combined with solubility data from lower pressure experiments. Further, our solubility determination agrees with melting point depression determined experimentally by Grove et al. (2006) for the H2O-saturated peridotite solidus at 1000 MPa. Melting point depression calculations were used to estimate H2O solubility in basalt along the experimentally determined H2O-saturated peridotite solidus. The results suggest that a linear relationship between H2O fugacity and the square of molar solubility exists up to ~1300 MPa, where there is an inflection point and solubility begins to increase less strongly with increasing H2O fugacity.  相似文献   
102.
Since the 1960s, an early explosive activity in the Mont-Dore Massif is associated with a major pyroclastic rhyolitic eruption (5–7 km3) known as the “Grande Nappe” (GN). This event, linked to the formation of a 6-km-diameter cryptic caldera named “Haute Dordogne”, was before our investigation dated by 40Ar/39Ar at 3.07 ± 0.04 Ma. Our new single-crystal laser fusion 40Ar/39Ar dates obtained on two outcrops of the GN (Rochefort-Montagne and Ludières) questioned several hypotheses made concerning this “landmark” event of the Mont-Dore Massif history. We demonstrate that: (1) the GN rhyolitic eruption has occurred much later than previously estimated (i.e. 2.77 ± 0.02–0.07 Ma full external uncertainties); (2) the correlation made between the Vendeix rhyolitic complexes (intra-caldera position) dated back to 2.74 ± 0.04 Ma and the GN is proposed; (3) xenocryst contamination could be very high (i.e. 70% for the Rochefort-Montagne GN outcrop) and explains the noticeable older age obtained previously; (4) a link between the GN eruption and the formation of a caldera is questionable; the hypothesis of a northward-oriented blast channeled eastward toward the paleo-Allier River is thus proposed.  相似文献   
103.
Nitrogen isotope values (δ15N) of surface sediments in the German Bight of the North Sea exhibit a significant gradient from values of 5–6‰ of the open shelf sea to values above 11‰ in the German Bight. This signal has been attributed to high reactive N (Nr) loading enriched in 15N from rivers and the atmosphere. To better understand the processes that determine the intensity and spatial distribution of δ15N anomalies in surface sediments, and to explore their usefulness for reconstructions of pristine N-input from rivers, we modeled the cycling of the stable isotopes 14N and 15N in reactive nitrogen through the ecosystem of the central and southern North Sea (50.9–57.3°N, 3.4°W−9.2°E) for the year 1995. The 3D-ecosystem model ECOHAM amended with an isotope-tracking module was validated by δ15N data of surface sediments within the model domain. A typical marine value (δ15Nnitrate=5‰) was prescribed for nitrate advected into the model domain at the seaside boundaries, whereas δ15Nnitrate of river inputs were those measured bi-monthly over 1 year; δ15N values of atmospheric deposition were set to 6‰ and 7‰ for NOx and NHy, respectively. The simulated δ15N values of different nitrogen compounds in the German Bight strongly depend on the mass transfers in the ecosystem. These fluxes, summarized in a nitrogen budget for 1995, give an estimate of the impacts of hydrodynamical and hydrological boundary conditions, and internal biogeochemical transformations on the nitrogen budget of the bight.  相似文献   
104.
A synthetic composition representing the Yamato 980459 martian basalt (shergottite) has been used to carry out phase relation, and rare earth element (REE) olivine and pyroxene partitioning experiments. Yamato 980459 is a sample of primitive basalt derived from a reduced end-member among martian mantle sources. Experiments carried out between 1-2 GPa and 1350-1650 °C simulate the estimated pressure-temperature conditions of basaltic melt generation in the martian mantle. Olivine-melt and orthopyroxene-melt partition coefficients for La, Nd, Sm, Eu, Gd and Yb (DREE values) were determined by LA-ICPMS, and are similar to the published values for terrestrial basaltic systems. We have not detected significant variation in D-values with pressure over the range investigated, and by comparison with previous studies carried out at lower pressure.We apply the experimentally obtained olivine-melt and orthopyroxene-melt DREE values to fractional crystallization and partial melting models to develop a three-stage geochemical model for the evolution of martian meteorites. In our model we propose two ancient (∼4.535 Ga) sources: the Nakhlite Source, located in the shallow mantle, and the Deep Mantle Source, located close to the martian core-mantle boundary. These two sources evolved distinctly on the ε143Nd evolution curve due to their different Sm/Nd ratios. By partially melting the Nakhlite Source at ∼1.3 Ga, we are able to produce a slightly depleted residue (Nakhlite Residue). The Nakhlite Residue is left undisturbed until ∼500 Ma, at which point the depleted Deep Mantle Source is brought up by a plume mechanism carrying with it high heat flow, melts and isotopic signatures of the deep mantle (e.g., ε182W, ε142Nd, etc.). The plume-derived Deep Mantle Source combines with the Nakhlite Residue producing a mixture that becomes a mantle source (herein referred to as “the Y98 source”) for Yamato 980459 and the other depleted shergottites with the characteristic range of Sm/Nd ratios of these meteorites. The same hot plume provides a heat source for the formation of enriched and intermediate shergottites. Our model reproduces the REE patterns of nakhlites and depleted shergottites and can explain high ε143Nd in depleted shergottites. Furthermore, the model results can be used to interpret whole rock Rb-Sr and Sm-Nd ages of shergottites.  相似文献   
105.
The Mesoscale Alpine Programme’s Riviera project investigated the turbulence structure and related exchange processes in an Alpine valley by combining a detailed experimental campaign with high-resolution numerical modelling. The present contribution reviews published material on the Riviera Valley’s boundary layer structure and discusses new material on the near-surface turbulence structure. The general conclusion of the project is that despite the large spatial variability of turbulence characteristics and the crucial influence of topography at all scales, the physical processes can accurately be understood and modelled. Nevertheless, many of the “text book characteristics” like the interaction between the valley and slope wind systems or the erosion of the nocturnal valley inversion need reconsideration, at least for small non-ideal valleys like the Riviera Valley. The project has identified new areas of research such as post-processing methods for turbulence variables in complex terrain and new approaches for the surface energy balance when advection is non-negligible. The exchange of moisture and heat between the valley atmosphere and the free troposphere is dominated by local “secondary” circulations due to the curvature of the valley axis. Because many curved valleys exist, and operational models still have rather poor resolution, parameterization of these processes may be required.  相似文献   
106.
We determined 15N/14N ratios of total nitrogen in surface sediments and dated sediment cores to reconstruct the history of N-loading of the North Sea. The isotopic N composition in modern surface sediments is equivalent to and reflects the isotopic mixture of oceanic nitrate on the one hand (δ15N = 5‰) and the imprint of river-borne nitrogen input into the SE North Sea (δ15N up to 12‰ in estuaries of the SE North Sea) on the other hand. We compare the results with δ15N records from pre-industrial sediment intervals in cores from the Skagerrak and Kattegat areas, which both constitute significant depositional centres for N in the North Sea and the Baltic Sea/North Sea transition. As expected, isotopically enriched anthropogenic nitrogen was found in the two records from the Kattegat area, which is close to eutrophication sources on land. Enrichment of δ15N in cores from the Skagerrak – the largest sediment sink for nitrogen in the entire North Sea – was not significant and values were similar to those found in sediment layers representing pre-industrial conditions. We interpret this isotopic uniformity as an indication that most riverine reactive nitrogen with its characteristic isotopic signature is removed by denitrification in shallow shallow-water sediments before reaching the main sedimentary basin of the North Sea.  相似文献   
107.
The structure, symmetry and origin of the incommensurately modulated OS phase of tridymite (SiO2) and its lock-in to the OP three-fold superlattice structure are discussed in a computational study. The structure of the OS phase (which has not been determined experimentally) is deduced as the only geometrically possible structure derived from the parent OC phase by rotation and translation of the SiO4 tetrahedra without significant distortion of these units. It can be visualised conveniently in terms of the McConnell formalism of two component difference structures C1 and C2 whose space group symmetries are derived. The results are in accordance with the known lock-in structure at wave vector Q= a *. In the latter, the ±C1 regions expand and the structure can square up in a very general way to take advantage of the lost symmetries (lost compared with the OC phase). Received: 4 August 1997 / Revised, accepted 24 November 1997  相似文献   
108.
The distribution of Mg, Mn, Fe, Co and Ni among olivine, orthopyroxene, calcic clinopyroxene and liquid can be described by exchange reactions of the form: M (phase A) + Mg (phase B) = M (phase B) + Mg (phase A). The thermochemical data predict the observed partitioning within the limits of error of both sets of data when assumptions of ideal solid solution are used, except for Mn-Mg exchange. Because ΔS and ΔV for these exchange reactions are generally small, KD varies relatively little with temperature and pressure, although individual ion distribution coefficients (D values) are more sensitive to these variables and to changing liquid composition.Trace elements present at the ppm level can enter crystals in normal lattice sites, can participate in point defect equilibria and can enter various defect sites present metastably in the crystal as a result of its P,T history. Metastable defect equilibria, in which the number of sites (grain boundaries, surfaces, intergrowths, etc.) is fixed, can lead to enhanced trace element solubility in the crystal at very low concentrations and thus to apparent deviations from Henry's law.  相似文献   
109.
110.
Nutrient and oxygen data collected in the southern Aegean Sea (Cretan Sea) and the straits of the Cretan Arc, during the four seasonal PELAGOS cruises in 1994–1995, are investigated and compared with data collected from 1987 to 1992 within the same area. During the cruises of the PELAGOS Project, nutrient enrichment of the intermediate layers of the Cretan Sea was observed, as a result of intrusion of ‘nutrient-rich, oxygen-poor’ Transition Mediterranean Water (TMW) compensating the Cretan Deep Water (CDW) outflow. TMW occupied the intermediate layers of the entire Cretan Sea. The concentrations of nutrients within this layer were often two times higher than those observed in the same area during previous studies undertaken before 1992 (increase 2.5 μmol/l of nitrate, 0.05 μmol/l of phosphate and 2.5μmol/l of silicate). The decrease of oxygen in this layer is about 0.8ml/l (35 μmol/l). Outflow of CDW occurs principally through the Antikithira and Kassos Straits (the two deeper straits of the Cretan Arc); it results in an increase of oxygen content but a decrease in the nutrient content of water in the deep and bottom layers outside the Cretan Sea. The major mesoscale features in the area have a major influence of the distributions and exchanges of nutrients and oxygen through the straits of the Cretan Arc. The surface and the intermediate layers were richer in nutrients and poorer in oxygen in spring (March 1994), than in autumn (September 1994).  相似文献   
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