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101.
The determination of the ephemeris of the Martian moons has benefited from observations of their plane-of-sky positions derived from images taken by cameras onboard spacecraft orbiting Mars. Images obtained by the Super Resolution Camera (SRC) onboard Mars Express (MEX) have been used to derive moon positions relative to Mars on the basis of a fit of a complete dynamical model of their motion around Mars. Since, these positions are computed from the relative position of the spacecraft when the images are taken, those positions need to be known as accurately as possible. An accurate MEX orbit is obtained by fitting two years of tracking data of the Mars Express Radio Science (MaRS) experiment onboard MEX. The average accuracy of the orbits has been estimated to be around 20–25 m. From these orbits, we have re-derived the positions of Phobos and Deimos at the epoch of the SRC observations and compared them with the positions derived by using the MEX orbits provided by the ESOC navigation team. After fit of the orbital model of Phobos and Deimos, the gain in precision in the Phobos position is roughly 30 m, corresponding to the estimated gain of accuracy of the MEX orbits. A new solution of the GM of the Martian moons has also been obtained from the accurate MEX orbits, which is consistent with previous solutions and, for Phobos, is more precise than the solution from the Mars Global Surveyor (MGS) and Mars Odyssey (ODY) tracking data. It will be further improved with data from MEX-Phobos closer encounters (at a distance less than 300 km). This study also demonstrates the advantage of combining observations of the moon positions from a spacecraft and from the Earth to assess the real accuracy of the spacecraft orbit. In turn, the natural satellite ephemerides can be improved and participate to a better knowledge of the origin and evolution of the Martian moons.  相似文献   
102.
Environmental concerns regarding the potential for drinking water contamination in shallow aquifers have accompanied unconventional energy development in the northern Appalachian Basin. These activities have also raised several critical questions about the hydrogeological parameters that control the naturally occurring presence and migration of hydrocarbon gases in shallow aquifers within petroliferous basins. To interrogate these factors, we analyzed the noble gas, dissolved ion, and hydrocarbon gas (molecular and isotopic composition) geochemistry of 98 groundwater samples from south‐central New York. All samples were collected ?1km from unconventional drilling activities and sample locations were intentionally targeted based on their proximity to various types of documented fault systems. In agreement with studies from other petroliferous basins, our results show significant correlations between elevated levels of radiogenic [4He], thermogenic [CH4], and dissolved ions (e.g., Cl, Br, Sr, Ba). In combination, our data suggest that faults have facilitated the transport of exogenous hydrocarbon‐rich brines from Devonian source rocks into overlying Upper Devonian aquifer lithologies over geologic time. These data conflict with previous reports, which conclude that hydrodynamic focusing regulates the occurrence of methane and salt in shallow aquifers and leads to elevated levels of these species in restricted flow zones within valley bottoms. Instead, our data suggest that faults in Paleozoic rocks play a fundamental role in gas and brine transport from depth, regulate the distribution of their occurrence in shallow aquifers, and influence the geochemistry of shallow groundwater in this petroliferous basin.  相似文献   
103.
104.
We use the results of elevated pressure melting experiments to constrain the role of melt/mantle reaction in the formation of tholeiitic magma from Kilauea volcano, Hawaii. Trace element abundance data is commonly interpreted as evidence that Kilauea tholeiite is produced by partial melting of garnet lherzolite. We experimentally determine the liquidus relations of a tightly constrained estimate of primary tholeiite composition, and find that it is not in equilibrium on its liquidus with a garnet lherzolite assemblage at any pressure. The composition is, however, cosaturated on its liquidus with olivine and orthopyroxene at 1.4 GPa and 1425 °C, from which we infer that primary tholeiite is in equilibrium with harzburgite at lithospheric depths beneath Kilauea. These results are consistent with our observation that tholeiite primary magmas have higher normative silica contents than experimentally produced melts of garnet lherzolite. A model is presented whereby primary tholeiite forms via a two-stage process. In the first stage, magmas are generated by melting of garnet lherzolite in a mantle plume. In the second stage, the ascent and decompression of magmas causes them to react with harzburgite in the mantle by assimilating orthopyroxene and crystallizing olivine. This reaction can produce typical tholeiite primary magmas from significantly less siliceous garnet lherzolite melts, and is consistent with the shift in liquidus boundaries that accompanies decompression of an ascending magma. We determine the proportion of reactants by major element mass balance. The ratio of mass assimilated to mass crystallized (Ma/Mc) varies from 2.7 to 1.4, depending on the primary magma composition. We use an AFC calculation to model the effect of melt/harzburgite reaction on melt rare earth and high field strength element abundances, and find that reaction dilutes, but does not significantly fractionate, the abundances of these elements. Assuming olivine and orthopyroxene have similar heats of fusion, the Ma/Mc ratio indicates that reaction is endothermic. The additional thermal energy is supplied by the melt, which becomes superheated during adiabatic ascent and can provide more thermal energy than required. Melt/harzburgite reaction likely occurs over a range of depths, and we infer a mean depth of 42 km from our experimental results. This depth is well within the lithosphere beneath Kilauea. Since geochemical evidence indicates that melt/harzburgite reaction likely occurs in the top of the Hawaiian plume, the plume must be able to thin a significant portion of the lithosphere. Received: 4 February 1997 / Accepted: 27 August 1997  相似文献   
105.
The development of effective environmental management plans and policies requires a sound understanding of the driving forces involved in shaping and altering the structure and function of ecosystems. However, driving forces, especially anthropogenic ones, are defined and operate at multiple administrative levels, which do not always match ecological scales. This paper presents an innovative methodology of analysing drivers of change by developing a typology of scale sensitivity of drivers that classifies and describes the way they operate across multiple administrative levels. Scale sensitivity varies considerably among drivers, which can be classified into five broad categories depending on the response of ‘evenness’ and ‘intensity change’ when moving across administrative levels. Indirect drivers tend to show low scale sensitivity, whereas direct drivers show high scale sensitivity, as they operate in a non-linear way across the administrative scale. Thus policies addressing direct drivers of change, in particular, need to take scale into consideration during their formulation. Moreover, such policies must have a strong spatial focus, which can be achieved either by encouraging local–regional policy making or by introducing high flexibility in (inter)national policies to accommodate increased differentiation at lower administrative levels. High quality data is available for several drivers, however, the availability of consistent data at all levels for non-anthropogenic drivers is a major constraint to mapping and assessing their scale sensitivity. This lack of data may hinder effective policy making for environmental management, since it restricts the ability to fully account for scale sensitivity of natural drivers in policy design.  相似文献   
106.
The closure of the Hawaiian longline swordfish fishery over the period 2001–2004, which was motivated by the protection of endangered sea turtles, created the elements of a natural experiment that allows identification of the market transfer of catch (and sea turtle bycatch) to other regions. This paper exploits the fact that the vessels in the Hawaiian longline fishery sell their catch in the US fresh swordfish market to analyze the pattern of changes in US fresh and frozen swordfish consumption both before and after the closure regulation was imposed. The mechanisms by which any unintended consequences on endangered sea turtles in other fishery locations in the world are shown to take place through the US swordfish market. At the estimated annual market transfer, a bootstrap analysis of the probability distribution of bycatch rates indicates that the regulation led to an additional 2882 sea turtle interactions at the sample means.  相似文献   
107.
The beginnings of hydrous mantle wedge melting   总被引:5,自引:3,他引:2  
This study presents new phase equilibrium data on primitive mantle peridotite (0.33 wt% Na2O, 0.03 wt% K2O) in the presence of excess H2O (14.5 wt% H2O) from 740 to 1,200°C at 3.2–6 GPa. Based on textural and chemical evidence, we find that the H2O-saturated peridotite solidus remains isothermal between 800 and 820°C at 3–6 GPa. We identify both quenched solute from the H2O-rich fluid phase and quenched silicate melt in supersolidus experiments. Chlorite is stable on and above the H2O-saturated solidus from 2 to 3.6 GPa, and chlorite peridotite melting experiments (containing ~6 wt% chlorite) show that melting occurs at the chlorite-out boundary over this pressure range, which is within 20°C of the H2O-saturated melting curve. Chlorite can therefore provide sufficient H2O upon breakdown to trigger dehydration melting in the mantle wedge or perpetuate ongoing H2O-saturated melting. Constraints from recent geodynamic models of hot subduction zones like Cascadia suggest that significantly more H2O is fluxed from the subducting slab near 100 km depth than can be bound in a layer of chloritized peridotite ~ 1 km thick at the base of the mantle wedge. Therefore, the dehydration of serpentinized mantle in the subducted lithosphere supplies free H2O to trigger melting at the H2O-saturated solidus in the lowermost mantle wedge. Alternatively, in cool subduction zones like the Northern Marianas, a layer of chloritized peridotite up to 1.5 km thick could contain all the H2O fluxed from the slab every million years near 100 km depth, which suggests that the dominant form of melting below arcs in cool subduction zones is chlorite dehydration melting. Slab PT paths from recent geodynamic models also allow for melts of subducted sediment, oceanic crust, and/or sediment diapirs to interact with hydrous mantle melts within the mantle wedge at intermediate to hot subduction zones.  相似文献   
108.
The comment of Stalder raises three main concerns regarding the interpretation of the experiments presented by Till et al. (2012): (1) our inability to uniquely distinguish between high-pressure hydrous silicate melt and solute-rich aqueous fluid leads to the incorrect interpretation of phase relations, (2) the temperature interval over which hydrous melting takes places is inordinately large and contrary to expectations, and/or (3) the possibility that the system may be above the second critical end point (SCEP) in this H2O-rich silicate system has been insufficiently discussed. In this reply, we provide clarification on these concerns and argue that with the extent of knowledge available today, the chemical characteristics of our experimental products at 3.2 and 4?GPa evince the presence of a silicate melt at temperatures <1,000?°C and we are below the SCEP in the peridotite–H2O system at the P–T conditions of our experiments. If in fact the quench observed in our experiments does represent that of a supercritical (SC) fluid, then our data suggest Mg and Fe are highly soluble in SC fluids at the P–T conditions of the base of the mantle wedge below arc volcanoes. Therefore, our results would require a significant change in thinking about the chemical compositional characteristics of SC fluids.  相似文献   
109.
Abstract— Phase equilibrium experiments on the most magnesian Apollo 15C green picritic glass composition indicate a multiple saturation point with olivine and orthopyroxene at 1520°C and 1.3 GPa (about 260 km depth in the moon). This composition has the highest Mg# of any lunar picritic glass and the shallowest multiple saturation point. Experiments on an Apollo 15A composition indicate a multiple saturation point with olivine and orthopyroxene at 1520°C and 2.2 GPa (about 440 km depth in the moon). The importance of the distinctive compositional trends of the Apollo 15 groups A, B, and C picritic glasses merits the reanalysis of NASA slide 15426,72 with modern electron microprobe techniques. We confirm the compositional trends reported by Delano (1979, 1986) in the major element oxides SiO2, TiO2, Al2O3, Cr2O3, FeO, MnO, MgO, and CaO, and we also obtained data for the trace elements P2O5, K2O, Na2O, NiO, S, Cu, Cl, Zn, and F. Petrogenetic modeling demonstrates that the Apollo 15 A‐B‐C glass trends could not have been formed by fractional crystallization or any continuous assimilation/fractional crystallization (AFC) process. The B and C glass compositional trends could not have been formed by batch or incremental melting of an olivine + orthopyroxene source or any other homogeneous source, though the A glasses may have been formed by congruent melting over a small pressure range at depth. The B compositional trend is well modeled by starting with an intermediate A composition and assimilating a shallower, melted cumulate, and the C compositional trend is well modeled by a second assimilation event. The assimilation process envisioned is one in which heat and mass transfer were separated in space and time. In an initial intrusive event, a picritic magma crystallized and provided heat to melt magma ocean cumulates. In a later replenishment event, the picritic magma incrementally mixed with the melted cumulate (creating the compositional trends in the green glass data set), ascended to the lunar surface, and erupted as a fire fountain. A barometer created from multiple saturation points provides a depth estimate of other glasses in the A‐B‐C trend and of the depths of assimilation. This barometer demonstrates that the Apollo 15 A‐B‐C trend originated over a depth range of ?460 km to ?260 km within the moon.  相似文献   
110.
We report results from multiwavelength observations of the microquasarGRS 1915+105 performed during the 2000 April campaign. This is one ofthe biggest campaigns ever made for this source covering the broadband from radio to γ-rays. Multiwavelength light curves compiledfrom all the data reduced up to date and broad band spectra obtainedwith ASCA and RXTE are presented.  相似文献   
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