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1.
Los Angeles is often described as the epitome of urban fragmentation, a notion which in this context is frequently connected to, or even conflated with urban sprawl. At the same time, the city features integrated water and power networks which have been under public ownership for over 70 years. We thus have an apparent paradox in the context of the debate on ‘splintering urbanism’, between socio-spatial fragmentation and the integration of networks. In discussing the idea that deregulation of infrastructural networks exacerbates urban fragmentation, the authors use the case of Los Angeles in order to highlight the central role of private interests in management decisions concerning infrastructure networks. The authors carry out their analysis in an historical perspective, revealing that network integration and universal access can often serve private interests more than the public good. Urban fragmentation in Los Angeles, they conclude, is the result of a complex process of instrumentalisation of network development and management.  相似文献   
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 Apatite is a relatively common accessory mineral in the olivine-bearing zones (OB-III and OB-IV) of the Middle Banded series of the Stillwater complex, occurring interstitial to cumulus grains, as monomineralic inclusions in cumulus grains, and in polymineralic clusters which may or may not be included in the cumulus grains. Eighty-nine of 185 samples examined were found to contain some apatite. The F-Cl-OH content of the apatite show distinct stratigraphic variations. XClAp (mole fraction Cl in apatite) of interstitial apatite increases upsection in both OB-III and OB-IV with average values ranging from 0.15 to 0.85 in OB-III and from 0.03 to 0.60 in OB-IV. XFAp varies inversely with XClApwith average values ranging from 0.00 to 0.70, while XOHAp remains relatively constant near 0.40 or decreases slightly with height. These variations are remarkable given that no appreciable stratigraphic variations in either the major or trace element compositions of any of the cumulus minerals are found in the 800 m of section that comprise OB-III and OB-IV. Within-sample variation of XClAp for samples containing Cl-rich apatite is substantially larger (up to 0.65 XClAp) than for samples with more F-rich apatite (XClAp varies by approximately 0.15). Although interstitial apatite is found throughout OB-III and OB-IV, apatite occurring as monomineralic inclusion in cumulus grains or in polymineralic clusters is almost exclusively found in samples with Cl-rich apatite. The data are best explained by a model involving the degassing of a Cl-rich volatile phase from the crystallizing interstitial liquid. The up-section migration of this fluid resulted in the crystallization of F-rich apatite in the lower portion and progressive Cl-enrichment in the apatite with height. The presence of hornblende-bearing dikes, veins and pegmatoids at the level of maximum Cl-enrichment is consistent with a fluid migration model. Received: 5 October 1995 / Accepted: 19 March 1996  相似文献   
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The diffusion of an ion in porewaters cannot occur independently of the other ions in solution as a result of Coulombic coupling, as well as from other effects not considered here. Unfortunately, a longstanding disagreement exists about the correct form and meaning of the equations that describe Coulombic coupling in porewaters, i.e., Ben-Yaakov [Am. J. Sci. 281 (1981) 974] vs. Lasaga [Am. J. Sci. 281 (1981) 981]. This paper re-examines this controversy by reformulating the problem starting from fundamental concepts of mass and charge conservation. We show that these antagonistic formulations are both valid and, in fact, equivalent, when the different interpretations of charge balance are resolved. Most of the disagreements between Ben-Yaakov and Lasaga are then shown to result from differing methods of solution, not fundamental disparities in their models. We note, however, that the explanation for the concept of “stationary” gradients of nonreacting ions as given Ben-Yaakov is inaccurate, and such gradients do lead to diffusive fluxes that are counterbalanced by electrochemical migrational fluxes to produce no net flux (excluding advective flux). We further find that the bicarbonate diffusive flux will not balance the diffusional charge flux of sulfate during its reduction if advection is present. This latter imbalance generates compensating fluxes in the other nonreacting ions. We have applied our theory to a simplified case of sulfate reduction in a marine sediment. The results show that nonreacting ions do diffuse and that with normally expected values of porewater advection, the ratio of the bicarbonate to the sulfate flux can be far different than the ideal value of −2.  相似文献   
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Bubble-induced porewater mixing: A 3-D model for deep porewater irrigation   总被引:1,自引:0,他引:1  
Porewater data from vent sites of the northeastern shelf off Sakhalin Island, Sea of Okhotsk, exhibit bottom-water concentrations down to a sediment depth of up to 300 cm. Below this depth, solute concentrations rapidly change due to methanogenesis and anaerobic methane oxidation (AMO). The profile shapes suggest an irrigation-like process that mixes on a meter scale. At these sites active gas emanation into the overlying water column and near-surface gas hydrates are commonly observed. We propose that methane gas bubbles rise through the soft surface sediments and cause mixing of the porewater.Mathematically, the bubble-induced irrigation can be described by eddy diffusion enhancing the diffusive transport of solutes by several orders of magnitude. A 3-D numerical transport-reaction model was developed to investigate the parameters defining the mixing process, such as bubble rise velocity, tube size, tube distribution in the sediment, and ebullition frequency.Model consistency with the field data requires eddy diffusivities ?1 × 105 cm2/a, tube densities of >4 tubes/m2 (equivalent to a tube spacing of <40 cm), active gas seepage for more than a few weeks or months, and moderate to low diagenetic reaction rates of solutes. The corresponding methane gas fluxes that are predicted from the results of the model realizations range from 1 × 103-5 × 105 L/(m2 a). Due to bubble mixing, solute fluxes in these sediments are increased by a factor of 3 and the maximum AMO rate by a factor of 7.  相似文献   
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Poisson’s ratio (static) appears as a parameter in models of soft-sediment geomechanical processes such as gas bubble formation and bioturbation, and in a number of practical applications, including acoustic imaging, but is rarely measured in soft near-surface (upper 20 cm) marine sediments. A new uniaxial apparatus was developed to assess Poisson’s ratios of cylindrical samples of soft cohesive sediments under finite-strain, unconfined, undrained conditions. No constraining membrane around the sample is necessary in the instrument. By monitoring the fluid level in a capillary, changes in sample volume can be determined to high precision (reproducibility). Measurements on reference materials, i.e., gelatine and polyurethane, also indicate high accuracy (veracity). For natural sediments from Nova Scotia, Canada, Poisson’s ratios range from 0.4951 to 0.5 with no indication of anisotropy; therefore, such sediments act as incompressible solids to short-term/small-magnitude stresses, as occur during bubble formation and infaunal movement.  相似文献   
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In situ tensile fracture toughness of surficial cohesive marine sediments   总被引:1,自引:1,他引:0  
This study reports the first in situ measurements of tensile fracture toughness, K IC, of soft, surficial, cohesive marine sediments. A newly developed probe continuously measures the stress required to cause tensile failure in sediments to depths of up to 1 m. Probe measurements are in agreement with standard laboratory methods of K IC measurements in both potter’s clay and natural sediments. The data comprise in situ depth profiles from three field sites in Nova Scotia, Canada. Measured K IC at two muddy sites (median grain size of 23–50 μm) range from near zero at the sediment surface to >1,800 Pa m1/2 at 0.2 m depth. These profiles also appear to identify the bioturbated/mixed depth. K IC for a sandy site (>90% sand) is an order of magnitude lower than for the muddy sediments, and reflects the lack of cohesion/adhesion. A comparison of K IC, median grain size, and porosity in muddy sediments indicates that consolidation increases fracture strength, whereas inclusion of sand causes weakening; thus, sand-bearing layers can be easily identified in K IC profiles. K IC and vane-measured shear strength correlate strongly, which suggests that the vane measurements should perhaps be interpreted as shear fracture toughness, rather than shear strength. Comparison of in situ probe-measured values with K IC of soils and gelatin shows that sediments have a K IC range intermediate between denser compacted soils and softer, elastic gelatin.  相似文献   
9.
Progressive leaching of plagioclase for Sr isotopes and microdrilling for Sr and Pb isotopes from grains of plagioclase and orthopyroxene from the Critical Zone and the Lower Zone indicates that these minerals are not in isotopic equilibrium. Leaching suggests Critical Zone plagioclase either lost Rb or had a more radiogenic Sri rim relative to the core, whereas plagioclase from an Upper Zone sample is isotopically homogeneous for Sri. Microdrilling analyses of plagioclase from the Lower and Critical Zones consistently have a higher initial 87Sr/86Sr (Sri) and a less radiogenic modeled 238U/204Pb composition (μ2) than coexisting orthopyroxene. The range of calculated Sri for plagioclase and orthopyroxene is 0.70506–0.70662(34) and 0.70290–0.70654(36), respectively. The average difference in Sri between mineral pairs was 0.00095. The range of calculated μ2 for plagioclase and orthopyroxene is 9.42–10.30 (average 9.7) and 9.83–15.75 (average 10.1), respectively. The range of measured 208Pb/206Pb for plagioclase and orthopyroxene is 34.757–36.439(33) and 36.669–41.845(85), respectively. One orthopyroxenite without evidence for more than one population of crystal size distribution, nonetheless had Sri = 0.70654 (36) with calculated μ2 of 10.32 for larger grains as compared with Sri = 0.70290 (32) and calculated μ2 of 9.97 for smaller grain-size fractions. Isotopic results from this study demonstrate that whole-rock isotopic data may not provide the appropriate level of detail necessary to address some processes in the Bushveld Complex. However, systematic changes have the potential to elucidate the timing of contamination with regard to other processes (crystal aging, compaction-driven recrystallization, and mineral exsolution) occurring within a slowly cooled crystal–liquid–vapor mush system.  相似文献   
10.
The use of chemical oil dispersants to minimize spill impacts causes a transient increase in hydrocarbon concentrations in water, which increases the risk to aquatic species if toxic components become more bioavailable. The risk of effects depends on the extent to which dispersants enhance the exposure to toxic components, such as polycyclic aromatic hydrocarbons (PAH). Increased salinities can reduce the solubility of PAH and the efficiency of oil dispersants. This study measured changes in the induction of CYP1A enzymes of fish to demonstrate the effect of salinity on PAH availability. Freshwater rainbow trout and euryhaline mummichog were exposed to water accommodated fractions (WAF), and chemically-enhanced water accommodated fractions (CEWAF) at 0 per thousand, 15 per thousand, and 30 per thousand salinity. For both species, PAH exposure decreased as salinity increased whereas dispersant effectiveness decreased only at the highest salinity. Hence, risks to fish of PAH from dispersed oil will be greatest in coastal waters where salinities are low.  相似文献   
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