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81.
Ocean Dynamics - Long-lived and large-scale anticyclonic Aleutian eddies (AEs), detaching from the Alaskan Stream to the west of 180∘ and propagating southwestward or almost zonally in the...  相似文献   
82.
In this paper we summarise the photo-physiological responses of phytoplankton to upwelling of macronutrients in mesoscale eddies in the subtropical North Atlantic (EDDIES project, Sargasso Sea) and subtropical North Pacific (E-FLUX project, Hawaii). The observations, obtained on two sets of cruises over 2 years, occupied six cyclonic eddies and two mode-water eddies. The photosynthetic physiological parameters were measured using a bench-top fluorescence induction and relaxation (FIRe) system and a submersible in situ fast repetition rate fluorometer (FRRF) deployed on an undulating towed vehicle. Both of these instruments were used to provide highly sensitive and well-resolved data on community responses. The responses are dependent on both the type of eddy and its stage of development. Our results indicate that, while cyclonic eddies in the Atlantic and Pacific can increase primary photosynthetic production early in their development, mode-water eddies in the subtropical North Atlantic can support patchy blooms of large diatoms for long periods of time (more than 3 months).  相似文献   
83.
The southward near-surface transport of transformed subarctic water across the Subpolar Front in the Japan Sea is simulated and analyzed based on altimeter data from January 1, 1993 to December 31, 2017. Computing Lagrangian indicators for a large number of synthetic particles, advected by the AVISO velocity field, we find preferred transport pathways across the Subpolar Front. The southward transport occurs mainly in the central part of the frontal zone due to suitable dispositions of mesoscale eddies promoting propagation of subarctic water to the south. It is documented with the help of Lagrangian origin and L-maps and verified by the tracks of available drifters. The transport of transformed subarctic water to the south is compared with the transport of transformed subtropical water to the north simulated by Prants et al. (Nonlinear Process Geophys 24(1):89–99, 2017c).  相似文献   
84.
Zhang  Yihuai  Lebedev  Maxim  Smith  Gregory  Jing  Yu  Busch  Andreas  Iglauer  Stefan 《Natural Resources Research》2020,29(3):1787-1800

Characterization of coal micro-structure and the associated rock mechanical properties are of key importance for coal seam exploration, coal bed methane development, enhanced coal bed methane production and CO2 storage in deep coal seams. Considerable knowledge exists about coal chemical properties, but less is known about the nanoscale to the micro-scale structure of coals and how they change with coal strength across coal ranks. Thus, in this study, 3D X-ray micro-computed tomography (with a voxel size of 3.43 µm) and nano-indentation tests were conducted on coal samples of different ranks from peat to anthracite. The micro-structure of peats showed a well-developed pore system with meso- and micro-pores. The meso-pores essentially disappear with increasing rank, whereas the micro-pores persist and then increase past the bituminous rank. The micro-fracture system develops past the peat stage and by sub-bituminous ranks and changes into larger and mature fracture systems at higher ranks. The nano-indentation modulus showed the increasing trend from low- to high-rank coal with a perfect linear relationship with vitrinite reflectance and is highly correlated with carbon content as expected.

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85.
The nature and abundance of dislocations in quartz surrounding fluid inclusions were studied to obtain a better understanding of processes associated with fluid inclusion reequilibration. Synthetic fluid inclusions containing 10 wt% NaCl aqueous solution were formed in three samples at 700 °C and 5 kbar. One of the samples was quenched along an isochore to serve as a reference sample. The other two samples were quenched along a P-T path that generated internal pressures in excess of the confining pressure. The two samples were held at the final reequilibration P-T conditions of 625 °C and 2 kbar for 30 and 180 days, respectively. Following the experiments, microstructures associated with fluid inclusions were examined with the TEM. Quartz in healed fractures in the reference sample that was quenched isochorically shows a moderate dislocation activity. Quartz adjacent to reequilibrated fluid inclusions in the other two samples, however, showed a marked increase in dislocation activity compared to the un-reequilibrated sample. Deformation of the inclusion walls occurred anisotropically by expansion of mobile dislocations in their slip systems. Dislocation expansion was controlled by glide in the rhombohedral planes {1 0 1 1} that was restricted to narrow zones (≤3 μm) in the immediate vicinity of the fluid inclusion walls outside of the healed fracture plane. These plastic zones were observed after both short term (30 days) and long term (180 days) experiments and are attributed to hydrolytic weakening of quartz around fluid inclusions owing to diffusion of water into the quartz matrix during the experiment. The close spatial association of submicroscopic water bubbles with dislocations, and the rarity of water bubbles in the reference sample, show clearly that in both the 30 and 180 day experiments reequilibration involves water loss from the fluid inclusions. Our results indicate that synthetic fluid inclusions in this study recover (chemically and volumetrically), even at relatively fast experimental loading rates, such that internal stresses never reach the point of brittle failure. The driving force for fluid inclusion deformation involves two related mechanisms: plastic deformation of hydrolytically weakened wet quartz in the healed fracture, and water leakage associated with preexisting and strain-induced dislocations. Received: 5 May 1998 / Accepted: 10 February 2000  相似文献   
86.
87.
 We present a method for studying local stability of a solution to an inverse problem and evaluate the uncertainty in determining true values of particular observables. The investigation is done under the assumption that only the Gaussian part of fluctuations about the local minimum of the cost (likelihood) function is essential. Our approach is based on the spectral analysis of the Hessian operator associated with the cost function at its extremal point, and we put forward an effective iterative algorithm suitable for numerical implementation in the case of a computationally large problem. Received: 16 May 2001 / Accepted: 22 October 2001  相似文献   
88.
The chemical reduction of U(VI) by Fe(II) is a potentially important pathway for immobilization of uranium in subsurface environments. Although the presence of surfaces has been shown to catalyze the reaction between Fe(II) and U(VI) aqueous species, the mechanism(s) responsible for the enhanced reactivity remain ambiguous. To gain further insight into the U-Fe redox process at a complexing, non-conducting surface that is relevant to common organic phases in the environment, we studied suspensions containing combinations of 0.1 mM U(VI), 1.0 mM Fe(II), and 4.2 g/L carboxyl-functionalized polystyrene microspheres. Acid-base titrations were used to monitor protolytic reactions, and Fe K-edge and U L-edge X-ray absorption fine structure spectroscopy was used to determine the valence and atomic environment of the adsorbed Fe and U species. In the Fe + surface carboxyl system, a transition from monomeric to oligomeric Fe(II) surface species was observed between pH 7.5 and pH 8.4. In the U + surface carboxyl system, the U(VI) cation was adsorbed as a mononuclear uranyl-carboxyl complex at both pH 7.5 and 8.4. In the ternary U + Fe + surface carboxyl system, U(VI) was not reduced by the solvated or adsorbed Fe(II) at pH 7.5 over a 4-month period, whereas complete and rapid reduction to U(IV) nanoparticles occurred at pH 8.4. The U(IV) product reoxidized rapidly upon exposure to air, but it was stable over a 4-month period under anoxic conditions. Fe atoms were found in the local environment of the reduced U(IV) atoms at a distance of 3.56 Å. The U(IV)-Fe coordination is consistent with an inner-sphere electron transfer mechanism between the redox centers and involvement of Fe(II) atoms in both steps of the reduction from U(VI) to U(IV). The inability of Fe(II) to reduce U(VI) in solution and at pH 7.5 in the U + Fe + carboxyl system is explained by the formation of a transient, “dead-end” U(V)-Fe(III) complex that blocks the U(V) disproportionation pathway after the first electron transfer. The increased reactivity at pH 8.4 relative to pH 7.5 is explained by the reaction of U(VI) with an Fe(II) oligomer, whereby the bonds between Fe atoms facilitate the transfer of a second electron to the hypothetical U(V)-Fe(III) intermediate. We discuss how this mechanism may explain the commonly observed higher efficiency of uranyl reduction by adsorbed or structural Fe(II) relative to aqueous Fe(II).  相似文献   
89.
Petrophysical properties of carbonate reservoirs are less predictable than that of siliciclastic reservoirs. One of the main reasons for this is the physical and chemical interactions of carbonate rocks with pore fluids. Such interactions can significantly change the elastic properties of the rock matrix and grains, making the applicability of Gassmann's fluid substitution procedure debatable. This study is an attempt to understand the mechanisms of fluid‐rock interactions and the influence of these interactions on elastic parameters of carbonates. We performed precise indentation tests on Savonnières limestone at a microscale level under dry, distilled water, and n‐Decane saturated conditions. Our experiments display softening of the rock matrix after water saturation. We have found that mainly the ooid cortices, peloid nuclei and prismatic intergranular cement are affected by water flooding. We also observed a shear modulus reduction in Savonnières limestone in an experiment performed at ultrasonic frequencies. One of the most important results obtained in our experimental study is that the Gassmann fluid substitution theory might not always be applicable to predict the elastic moduli of fluid‐saturated limestones.  相似文献   
90.
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