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21.
He diffusion in olivine   总被引:1,自引:0,他引:1  
Helium diffusion in olivine (dunite xenolith) has been measured in the temperature range 1180–1460°C; a linear Arrhenius function was obtained with an activation energy of 120−27+32 kcal/mole, and a pre-exponential factor (D0) = 2.2 × 108 cm2/s.

Diffusion mechanisms are not a viable means of degassing He from the mantle. Olivine phenocrysts can be expected to retain previously trapped He, during cooling in extrusive basalts, provided the flow units are thinner than 50 m; xenoliths will retain mantle He signatures only if magma transport times are less than 50 years, or if the He fugacity in the magma is high enough to prevent xenolith degassing. The lower oceanic crust is probably substantially degassed of He. Trapped He will be qualitatively retained in quenched submarine basalt glass only if the cooling rate is faster than 5 × 1014°C/m.y.; glass at several centimeters depth in a basalt flow (near the spherulite zone) will have cooling rates lower than this, so He loss may be significant in many basalt glass samples.  相似文献   

22.
Cation exchange experiments (ammonium acetate and cation resin) on celadonite-smectite vein minerals from three DSDP holes demonstrate selective removal of common Sr relative to Rb and radiogenic Sr. This technique increases the Rb/Sr ratio by factors of 2.3 to 22 without significantly altering the age of the minerals, allowing easier and more precise dating of such vein minerals. The ages determined by this technique (site 261—121.4 ±1.6 m.y.; site 462A—105.1 ±2.8 m.y.; site 516F—69.9 ±2.4 m.y.) are 34, 54 and 18 m.y. younger, respectively, than the age of crust formation at the site; in the case of site 462A, the young age is clearly related to off-ridge emplacement of a massive sill/flow complex. At the other sites, either the hydrothermal circulation systems persisted longer than for normal crust (10–15 m.y.), or were reactivated by off-ridge igneous activity.

Celadonites show U and Pb contents and Pb isotopic compositions little changed from their basalt precursors, while Th contents are significantly lower. Celadonites thus have unusually high alkali/U,Th ratios and low Th/U ratios. If this celadonite alteration signature is significantly imprinted on oceanic crust as a whole, it will lead to very distinctive Pb isotope signatures for any hot spot magmas which contain a component of aged subducted recycled oceanic crust.

Initial Sr isotope ratios of ocean crust vein minerals (smectite, celadonite, zeolite, calcite) are intermediate between primary basalt values and contemporary sea water values and indicate formation under seawaterdominated systems with effective water/rock ratios of 20–200.  相似文献   

23.
Flourescence spectral analysis indicates that resinite macerals from Tertiary Hanna Formation coals (Hanna Coal Field, southcentral Wyoming, U.S.A.) can be separated into five distinct groups. The first resinite group fluoresces a a medium green (in blue light); its average spectral maximum occurs at or below 440 mm with a red/green quotient of 0.22. The second resinite group fluoresces yellow-green with an average spectral maximum of 500 nm and a red/green quotient of 0.53. The third resinite group displays a yellow fluorescence having an average spectral maximum of 580 nm and a red/green quotient of 0.86. The fourth resinite group fluorescence orange-brown having an average spectral maximum of 610 nm and a red/green quotient of 1.20. These four groups mostly occur as primary globular resinites exhibiting scratches and fractures, indicating that they are brittle, solid substances. Primary cell-filling and secondary fracture-filling resinites also occur in these four groups. The fifth group only occurs as a secondary void-filling material and lacks evidence of br of brittle properties. It fluoresces a reddish-brown, has a spectral maximum at 690 nm, and a red/green quotient of 1.54. The fifth group has properties resembling exsudatinite. The five resinite groups can be separated on the basis of their nine spectral properties alone, without qualitative petrographic interpretation.The relative quantities of the five resinite groups vary among Hanna Formation coals. The origins of these five resinite groups are probably related to their botanical properties and pre- and post-depossitional conditions. Overall, Hanna Formation resinites have petrographic characteristics similar to other North American resinites; however, only four resinite groups have been distinguished in in certain coals from Utah and New Mexico (U.S.A.), and western Canada.  相似文献   
24.
While the chemical structure of the earth's mantle is probably rather complex, multi-box models have been used as a first approximation to evaluate this structure. Most commonly, a three-box model is used, involving the continental crust, the upper mantle and the lower mantle. The depleted upper mantle and the continental crust are assumed to represe1nt complementary reservoirs, related by crust formation processes occurring during geologic history.Here we investigate the Rb/Sr and Sm/Nd isotopic systematics of several three-box models, using mass balance equations and the definition of the mean age of the reservoirs. The geochemical uniqueness of the models, chosen from a large family of possible models, is evaluated from elementary graph theory, and these models are then solved using a total inversion approach. This paper (Part I) describes the methodology of the procedure; the companion paper (Part II) discusses the application of this approach to multi-box mantle models.  相似文献   
25.
It is suggested that leakage currents flow across Devon, north of Exeter, from large-scale electric-current systems induced in the Atlantic Ocean by the geomagnetic variations incident on the Atlantic Ocean from the ionosphere. This model can account for the variation with period of the contribution of induced current flow to the differences in the magnetic H variations of period > 30 s observed at Exeter and Sidmouth.  相似文献   
26.
Alteration of basaltic glass to palagonite is characterized by a nearly isomolar exchange of SiO2, Al2O3, MnO, MgO, CaO, Na2O, P2O5, Zn, Cu, Ni, Cr, Hf, Sc, Co and REE for H2O and K2O, whilst TiO2 and FeO are passively accumulated during removal of the remaining cations. The network forming cations Al and Si are removed from the glass in proportion to the gain in Ti and Fe, whilst the other cations do not show a significant relationship to the amount of Ti and Fe accumulation. Sr isotopic data show that during palagonite formation approximately 85% of the basaltic Sr is lost to the hydrous solutions and 40% of seawater Sr is added to the glass, yielding an average loss of the same order of magnitude as of the network forming cations. Losses and gains of oxides yield an average increase of +105% TiO2.K, Rb, and Cs show high increases, but KRb and KCs ratios indicate two different alteration processes: (1) formation of palagonite involves a drastic decrease in these ratios, indicating structural similarities between palagonite and smectite; (2) surface alteration of glass is characterized by an increase in KRb and KCs ratios, probably best interpreted as sorption of alkalies in ratios approximating those of seawater.The total fluxes involved in alteration of glass in the upper portion of the oceanic crust are estimated from the modal abundance of palagonite in the oceanic crust and the abundance of the vein materials smectite and carbonate. Smectite and carbonates act as a sink for a significant portion of the elements liberated up during alteration of basaltic glass except for Na and Al, which are probably taken up by zeolites and/or albite, possibly hidden in the macroscopic estimate of carbonate. Formation of the observed quantity of secondary phases requires additional sources for Si, Fe. Ca and K. K is provided in excess from the inflowing seawater at reasonable water/rock ratios. The remaining excess Ca, Si and Fe required may be derived by alteration of interstitial glass and breakdown of anorthite rich plagioclase and titano-magnetite, and/or by supply of deeper seated metamorphic reactions.  相似文献   
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Large, recreationally or commercially important populations of Atlantic sturgeon (Acipenser oxyrinchus), American shad (Alosa sapidissima), and striped bass (Morone saxatilis) occur in the Hudson River. Members of the Hudson River populations of these fishes also occur over a broad range along the Atlantic coast where they mix with conspecifics from other anadromous populations. For management purposes, it is imperative to be able to discriminate among individual stocks so that weak stocks may be protected and harvest may be allocated equitably. Because of their sensitivity and resistance to environmentally-induced temporal variation, molecular approaches have been increasingly employed in stock identification studies. However, post-Pleistocene recolonization of the Hudson River must have occurred less than 10,000 years ago—a relatively brief period for genetic divergence among populations. We tested whether various measures of DNA variation between Hudson River populations and adjacent populations of Atlantic sturgeon, American shad, and striped bass were sufficient to discriminate among their conspecific populations. American shad populations surveyed for mtDNA variation were highly diverse genotypically, but genotypic frequencies among the populations of the Connecticut, Hudson, and Delaware rivers were statistically homogenous (p>0.05). In contrast, Atlantic sturgeon (surveyed for mtDNA variation) and striped bass (surveyed for mtDNA and nuclear DNA variation) populations of the Hudson River were not genotypically diverse, but they were differentiated from northern and southern populations. Our results suggest higher gene flow (and lesser homing fidelity) among American shad populations in comparison with the two other species.  相似文献   
30.
From mica fission-track maps the serpentinized and weathered portions of four ultramafic rocks from oceanic ridge systems contained 0.5 to 2.4 ppm U compared to only 2.5 ppb in clinopyroxene, 0.6 ppb in chromite and less than 7.0 ppb in olivine. Orthopyroxene grains contained 0.4 ppb U which is three orders of magnitude lower than had previously been reported.Long thin tracks from (n, α) reactions with boron were recorded in cellulose nitrate plastic and were counted like fission tracks. The track density from boron was 2×104 times higher than that from uranium fission alone. Boron in serpentine was variable on a 50-μm scale attaining 155 ppm concentrations. Orthopyroxene grains, in contrast, had maximum concentrations of 0.8 ppm.Most of the uranium and boron in the rocks is believed to have been introduced during serpentinization. From known crystal-melt partitioning ratios the uranium and boron distributions are consistent with the ultramafic rocks being cumulates or residues from partial melting events.  相似文献   
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