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101.
Beaver dam analogs (BDAs) are a stream restoration technique that is rapidly gaining popularity in the western United States. These low-cost, stream-spanning structures, designed after natural beaver dams, are being installed to confer the ecologic, hydrologic, and geomorphic benefits of beaver dams in streams that are often too degraded to provide suitable beaver habitat. BDAs are intended to slow streamflow, reduce the erosive power of the stream, and promote aggradation, making them attractive restoration tools in incised channels. Despite increasing adoption of BDAs, few studies to date have monitored the impacts of BDAs on channel form. Here, we examine the geomorphic changes that occurred within the first year of restoration efforts in Wyoming using high-resolution visible light orthomosaics and elevation data collected with unoccupied aerial vehicles (UAVs). By leveraging the advantages of rapidly acquired images from UAV surveys with recent advancements in structure-from-motion photogrammetry, we constructed centimeter-scale digital elevation models (DEMs) of the restoration reach and an upstream control reach. Through DEM differencing, we identified areas of enhanced erosion and deposition near the BDAs, suggesting BDA installation initiated a unique geomorphic response in the channel. Both reaches were characterized by net erosion during the first year of restoration efforts. While erosion around the BDAs may seem counter to the long-term goal of BDA-induced aggradation, short-term net erosion is consistent with high precipitation during the study and with theoretical channel evolution models of beaver-related stream restoration that predict initial channel widening and erosion before net deposition. To better understand the impacts of BDAs on channel morphology and restoration efforts in the western United States, it is imperative that we consistently assess the effects of beaver-inspired restoration projects across a range of hydrologic and geomorphic settings and that we continue this monitoring in the future.  相似文献   
102.
Nonpoint sources of nitrogen (N) and other nutrients are a major source of water pollution within the Chesapeake Bay watershed and other basins around the world. Human activities associated with agricultural practices can account for a large percentage of N loadings delivered to streams and rivers. This work aims to improve understanding of N transport from groundwater to surface waters, quantifying the principal hydrological processes driving water and N fluxes into and out of a headwater agricultural stream reach. The study site is a 175-m stream reach in a heavily cultivated 40-ha watershed in east-central Pennsylvania. This subwatershed is underlain by fractured shale bedrock, and receives most of its baseflow from groundwater, either by diffuse matrix discharge through the streambed or by localized discharge through riparian seeps. Samples of stream, seep, and shallow groundwater were collected approximately monthly under steady hydrologic conditions in 2017. Calculated matrix flow from hydraulic head and conductivity measurements paired with differential stream gauging was used to solve for the riparian seep flux using a mass balance approach. Riparian seep fluxes ranged from 45 to 217 m3/d, transporting 0.6–4.2 kg N d−1 of nitrate-N from the fractured bedrock aquifer to the stream. Hydrochemical data suggest that the stream is mainly disconnected from the underlying aquifer and that seeps supply essentially all water and N to the system. Seeps are likely sourced with N in nearby agricultural fields and accelerated through the system with shorter residence times than shallow groundwater. Water isotope data reinforced this notion. This study underscores the importance of agriculture as a source of N to ground and surface waters. Identifying source areas that are causing groundwater enrichment of N and seep areas where N discharges to streams is beneficial for developing N pollution mitigation strategies and implementing management practices that aim to reduce nutrient loads to the Chesapeake Bay.  相似文献   
103.
Issues concerning the structure and evolution of core collapse progenitor stars, and stellar evolution in general, are discussed with an emphasis on interior evolution. We discuss some recent results that address quantifying the uncertainties inherent in modern stellar evolution calculations, and we describe a research effort aimed at investigating the transport and mixing processes associated with stellar turbulence, which is arguably the greatest source of uncertainty in supernova progenitor structure, besides mass loss, at the time of core collapse. We highlight the important role played by precision observations of stellar parameters in constraining theoretical models, as well as the physical insight that can be garnered from three-dimensional hydrodynamic simulation.  相似文献   
104.
Sulfate-reducing bacteria (SRB) are ubiquitous in anoxic environments where they couple the oxidation of organic compounds to the production of hydrogen sulfide. This can be problematic for various industries including oil production where reservoir “souring” (the generation of H2S) requires corrective actions. Nitrate or nitrite injection into sour oil fields can promote SRB control by stimulating organotrophic nitrate- or nitrite-reducing bacteria (O-NRB) that out-compete SRB for electron donors (biocompetitive exclusion), and/or by lithotrophic nitrate- or nitrite-reducing sulfide oxidizing bacteria (NR-SOB) that remove H2S directly. Sulfur and oxygen isotope ratios of sulfide and sulfate were monitored in batch cultures and sulfidic bioreactors to evaluate mitigation of SRB activities by nitrate or nitrite injection. Sulfate reduction in batch cultures of Desulfovibrio sp. strain Lac15 indicated typical Rayleigh-type fractionation of sulfur isotopes during bacterial sulfate reduction (BSR) with lactate, whereas oxygen isotope ratios in unreacted sulfate remained constant. Sulfur isotope fractionation in batch cultures of the NR-SOB Thiomicrospira sp. strain CVO was minimal during the oxidation of sulfide to sulfate, which had δ18OSO4 values similar to that of the water-oxygen. Treating an up-flow bioreactor with increasing doses of nitrate to eliminate sulfide resulted in changes in sulfur isotope ratios of sulfate and sulfide but very little variation in oxygen isotope ratios of sulfate. These observations were similar to results obtained from SRB-only, but different from those of NR-SOB-only pure culture control experiments. This suggests that biocompetitive exclusion of SRB took place in the nitrate-injected bioreactor. In two replicate bioreactors treated with nitrite, less pronounced sulfur isotope fractionation and a slight decrease in δ18OSO4 were observed. This indicated that NR-SOB played a minor role during dosing with low nitrite and that biocompetitive exclusion was the major process. The results demonstrate that stable isotope data can contribute unique information for understanding complex microbial processes in nitrate- and sulfate-reducing systems, and offer important information for the management of H2S problems in oil reservoirs and elsewhere.  相似文献   
105.
We report rates of oxygen exchange with bulk solution for an aqueous complex, IVGeO4Al12(OH)24(OH2)128+(aq) (GeAl12), that is similar in structure to both the IVAlO4Al12(OH)24(OH2)127+(aq) (Al13) and IVGaO4Al12(OH)24(OH2)127+(aq) (GaAl12) molecules studied previously. All of these molecules have ε-Keggin-like structures, but in the GeAl12 molecule, occupancy of the central tetrahedral metal site by Ge(IV) results in a molecular charge of +8, rather than +7, as in the Al13 and GaAl12. Rates of exchange between oxygen sites in this molecule and bulk solution were measured over a temperature range of 274.5 to 289.5 K and 2.95 < pH < 4.58 using 17O-NMR.Apparent rate parameters for exchange of the bound water molecules (η-OH2) are kex298 = 200 (±100) s−1, ΔH = 46 (±8) kJ · mol−1, and ΔS = −46 (±24) J · mol−1 K−1 and are similar to those we measured previously for the GaAl12 and Al13 complexes. In contrast to the Al13 and GaAl12 molecules, we observe a small but significant pH dependence on rates of solvolysis that is not yet fully constrained and that indicates a contribution from the partly deprotonated GeAl12 species.The two topologically distinct μ2-OH sites in the GeAl12 molecule exchange at greatly differing rates. The more labile set of μ2-OH sites in the GeAl12 molecule exchange at a rate that is faster than can be measured by the 17O-NMR isotopic-equilibration technique. The second set of μ2-OH sites have rate parameters of kex298 = 6.6 (±0.2) · 10−4 s−1, ΔH = 82 (±2) kJ · mol−1, and ΔS = −29 (±7) J · mol−1 · K−1, corresponding to exchanges ≈40 and ≈1550 times, respectively, more rapid than the less labile μ2-OH sites in the Al13 and GaAl12 molecules. We find evidence of nearly first-order pH dependence on the rate of exchange of this μ2-OH site with bulk solution for the GeAl12 molecule, which contrasts with Al13 and GaAl12 molecules.  相似文献   
106.
Seven dives in the submersible ALVIN and four deep-towed (ANGUS) camera lowerings have been made at the eastern ridge-transform intersection of the Oceanographer Transform with the axis of the Mid-Atlantic Ridge. These data constrain our understanding of the processes that create and shape the distinctive morphology that is characteristic of slowly-slipping ridge-transform-ridge plate boundaries. Although the geological relationships observed in the rift valley floor in the study area are similar to those reported for the FAMOUS area, we observe a distinct change in the character of the rift valley floor with increasing proximity to the transform. Over a distance of approximately ten kilometers the volcanic constructional terrain becomes increasingly more disrupted by faulting and degraded by mass wasting. Moreover, proximal to the transform boundary, faults with orientations oblique to the trend of the rift valley are recognized. The morphology of the eastern rift valley wall is characterized by inward-facing scarps that are ridge-axis parallel, but the western rift valley wall, adjacent to the active transform zone, is characterized by a complex fault pattern defined by faults exhibiting a wide range of orientations. However, even for transform parallel faults no evidence for strike-slip displacement is observed throughout the study area and evidence for normal (dip-slip) displacement is ubiquitous. Basalts, semi-consolidated sediments (chalks, debris slide deposits) and serpentinized ultramafic rocks are recovered from localities within or proximal to the rift valley. The axis of accretion-principal transform displacement zone intersection is not clearly established, but appears to be located along the E-W trending, southern flank of the deep nodal basin that defines the intersection of the transform valley with the rift floor.  相似文献   
107.
Many mid-ocean ridge basalts (MORBs) might be ultimately derived from primary magmas that are very depleted in Na2O and TiO2. These very depleted primary magmas have 0.60 to 1.50 wt.% Na2O and 0.10 to 0.50 wt.% TiO2 compared to MORBs, which typically have > 1.90% Na2O and >0.60% TiO2. Evidence for these depleted primary magma compositions is obtained from megacrysts in MORBs, from glass inclusions within these megacrysts, and from the highly calcic plagioclases (An91–96) and depleted clinopyroxenes (Na2O mostly between 0.10 and 0.35) in certain abyssal peridotites.Cumulate ultramanfi and gabbroic rocks from the North Arm Mountain Massif of the Bay of Islands ophiolite complex show a progressive increase in the Na2O and TiO2 abundances in clinopyroxene crystals with stratigraphic height in the ophiolite. The use of mineral-liquid distribution coefficients and cumulate mineral compositions indicate that the liquids from which these minerals crystallized had 0.10 to 0.20 wt.% TiO2 and 0.60 to 0.80 wt.% Na2O for the lowermost cumulate ultramafic rocks, with TiO2 and Na2O abundances of liquids increasing progressively to normal MORB abundances during crystallization of higher-level gabbroic cumulates. These data clearly demonstrate that primary basalts that are very depleted in Na2O and TiO2 can differentiate to form residual magmas that are indistinguishable from MORBs.  相似文献   
108.
Partially serpentinized dunites and wehrlites comprise the bulk of the cumulate ultramafic unit at the North Arm Mountain massif of the Bay of Islands ophiolite complex, Newfoundland. In a suite of 59 dunites and werhlites from the base of the unit, the serpentinized portions consist of lizardite + chrysotile + brucite + (accessory) magnetite. The ratio of (lizardite + chrysotile) to brucite = ~8:2 (weight percent). Petrographic observations show that most serpentinization occurred at the expense of olivine; only limited amounts of clinopyroxene were serpentized. An estimated volume increase of 32% accompanied serpentinization of the peridotites. Reconstructions of the primary modal proportions of wehrlites (made taking this volume increase into account) contain an average of 6% more clinopyroxene and 6% less olivine than do modal reconstructions that ignore the volume increase. Mass balance calculations provide no clear evidence for appreciable metasomatism of Al2O3, CaO, FeO, MgO, or SiO2 during Serpentinization. The presence of brucite, the evidence that most serpentinization occurred at the expense of olivine, and the lack of appreciable metasomatism, suggest that the primary reaction that controlled serpentinization of the peridotites is: 2Mg2SiO2 + 3H2O ? Mg3Si2O5(OH)4 + Mg(OH)2. olivine added serpentine brucite  相似文献   
109.
The empirical rate laws formulated to describe the dissolution rates of oxide minerals include the surface charge concentration that results from the protonation and deprotonation of surface functional groups. Previous experiments on quartz and silica have shown that dissolution rates vary as a function of different background electrolyte solutions, however, such experiments are often conducted at elevated temperatures where it is difficult to estimate surface charge along with the dissolution rates. In the present study we measuresurface charge concentrations for silica in different electrolyte solutions at 298 K in order to quantify the extent to which the different counterions could affect the dissolution rates through their influence on the surface charge concentrations. The experimental solutions in the electrolyte series: LiCl, NaCl, KCl, RbCl, CaCl2, SrCl2 and BaCl2 were prepared to maintain a constant metal concentration of 1.0 M. For the alkali-metal chlorides, the surface charge concentrations correlate with the size of the hydrated alkali metal, consistent with the idea that these counterions affect charge via outer-sphere coordination that shield proton surface complexes from one another. The reactivity trend for alkaline-earth cations is less clear, but the data demonstrate distinct differences in the acid-base propertiesof the silica surface in these different electrolytes. We then discuss how these trends are manifested in the rate equations used to interpret dissolution experiments.  相似文献   
110.
This work examines future flood risk within the context of integrated climate and hydrologic modelling uncertainty. The research questions investigated are (1) whether hydrologic uncertainties are a significant source of uncertainty relative to other sources such as climate variability and change and (2) whether a statistical characterization of uncertainty from a lumped, conceptual hydrologic model is sufficient to account for hydrologic uncertainties in the modelling process. To investigate these questions, an ensemble of climate simulations are propagated through hydrologic models and then through a reservoir simulation model to delimit the range of flood protection under a wide array of climate conditions. Uncertainty in mean climate changes and internal climate variability are framed using a risk‐based methodology and are explored using a stochastic weather generator. To account for hydrologic uncertainty, two hydrologic models are considered, a conceptual, lumped parameter model and a distributed, physically based model. In the conceptual model, parameter and residual error uncertainties are quantified and propagated through the analysis using a Bayesian modelling framework. The approach is demonstrated in a case study for the Coralville Dam on the Iowa River, where recent, intense flooding has raised questions about potential impacts of climate change on flood protection adequacy. Results indicate that the uncertainty surrounding future flood risk from hydrologic modelling and internal climate variability can be of the same order of magnitude as climate change. Furthermore, statistical uncertainty in the conceptual hydrological model can capture the primary structural differences that emerge in flood damage estimates between the two hydrologic models. Copyright © 2014 John Wiley & Sons, Ltd.  相似文献   
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