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1.
OBS’s were deployed for 26 to 29 days in the eastern Bismarck Sea to investigate the back-arc spreading. Hypocenters of 186 shallow earthquakes were determined using P- and S-waves from at least five stations. In the western survey area, a transform fault zone is marked by a linear micro-earthquake activity striking N65°W and less than 5 km wide. The predominant type of their focal mechanisms is strike-slip. In the eastern area, several intermittent zones of micro-earthquakes and their strike-slip type focal mechanisms suggest the location of short-length transform faults separating en-echelon spreading ridges.  相似文献   
2.
Poisson's ratios of the upper and lower crust and the sub-Moho mantle beneath central Honshu, Japan, are investigated using three independent methods that are based on S to P ratios of apparent velocities, the Wadati diagrams and an inversion of P and S arrivals. Shallow earthquakes at distances of 200—500 km from the Nagoya University Telemeter Network are used for the apparent velocity ratio method. Crustal and subcrustal earth-quakes under the network are used for the other two methods. The network consists of wide-band seismometers with three components which are particularly suitable for detecting S waves. The three different methods give a consistent result for Poisson's ratio σ, that is, (1) σ = 0.23 ± 0.01 in the upper crust, (2) σ = 0.26−0.28 in both the lower crust and in the sub-Moho mantle. The result indicates a sharp contrast in σ between the upper and the lower crust rather than at the Moho. The low σ in the upper crust can only be explained by the presence of a substantial amount of free quartz, indicating granitic rocks. A higher σ in the lower crust suggests that this portion is presumably less saturated in silica and may be even undersaturated, pointing to intermediate to mafic rocks. The sub-Moho σ is almost equal to the σ averaged over the entire upper mantle that has been estimated from the Wadati diagrams of deep shocks beneath Japan but is higher than those calculated from Pn and Sn velocities in oceanic and stable continental regions.  相似文献   
3.
Abstract– We have developed new sample preparation and analytical techniques tailored for entire aerogel tracks of Wild 2 sample analyses both on “carrot” and “bulbous” tracks. We have successfully ultramicrotomed an entire track along its axis while preserving its original shape. This innovation allowed us to examine the distribution of fragments along the entire track from the entrance hole all the way to the terminal particle. The crystalline silicates we measured have Mg‐rich compositions and O isotopic compositions in the range of meteoritic materials, implying that they originated in the inner solar system. The terminal particle of the carrot track is a 16O‐rich forsteritic grain that may have formed in a similar environment as Ca‐, Al‐rich inclusions and amoeboid olivine aggregates in primitive carbonaceous chondrites. The track also contains submicron‐sized diamond grains likely formed in the solar system. Complex aromatic hydrocarbons distributed along aerogel tracks and in terminal particles. These organics are likely cometary but affected by shock heating.  相似文献   
4.
Abstract— The measurements of magnesium and potassium isotopic compositions of refractory minerals in Allende calcium‐aluminum‐rich inclusions (CAIs), 7R‐19–1, HN3–1, and EGG3 were taken by secondary ion mass spectrometry (SIMS). The 7R‐19–1 contains 16O‐rich and 16O‐poor melilite grains and define a single isochron corresponding to an initial 26Al/27Al ratio of (6.6 ± 1.3) × 10?5. The Al‐Mg isochron, O isotope measurements and petrography of melilite in 7R‐19–1 indicate that 16O‐poor melilite crystallized within 0.4 Myr after crystallization of 16O‐rich melilite, suggesting that oxygen isotopic composition of the CAI‐forming region changed from 16O‐rich to 16O‐poor within this time interval. The 16O‐poor melilite is highly depleted in K compared to the adjacent 16O‐rich melilite, indicating evaporation during remelting of 7R‐19–1. We determined the isochron for 41Ca‐41K isotopic systematics in EGG3 pyroxene with (4.1 ± 2.0) × 10?9 (2s?) as an initial ratio of 41Ca/40Ca, which is at least two times smaller than the previous result (Sahijipal et al. 2000). The ratio of 41Ca/40Ca in the EGG3 pyroxene grain agrees within error with the value obtained by Hutcheon et al. (1984). No evidence for the presence of 41K excess (decay product of a short‐lived radionuclide 41Ca) was found in 7R‐19–1 and HN3–1. We infer that the CAI had at least an order of magnitude lower than canonical 41Ca/40Ca ratio at the time of the CAI formation.  相似文献   
5.
Chemical compositions of materials used for new sample holders (vertically aligned carbon nanotubes [VACNTs] and polyimide film), which were developed for the analysis of Hayabusa2‐return samples, were determined by instrumental neutron activation analysis and/or instrumental photon activation analysis, to estimate contamination effects from the sample holders. The synthetic quartz plate used for the sample holders was also analyzed. Ten elements (Na, Al, Cr, Mn, Fe, Ni, Eu, W, Au, and Th) and 14 elements (Na, Al, K, Sc, Ti, Cr, Zn, Ga, Br, Sb, La, Eu, Ir, and Au) could be detected in the VACNTs and polyimide film, respectively. The VACNT data show that contamination by this material with respect to the Murchison meteorite is negligible in terms of the elemental ratios (e.g., Fe/Mn, Na/Al, and Mn/Cr) used for the classification of meteorites due to the extremely low density of VACNTs. However, for the Au/Cr ratio, even small degrees (1.7 wt%) of contamination by VACNTs will change the Au/Cr ratio. Elemental ratios used for the classification of meteorites are only influenced by large amounts of contamination (>60 wt%) of polyimide film, which is unlikely to occur. In contrast, detectable effects on Ti isotopic compositions are caused by >0.1 and >0.3 wt% contamination by VACNTs and polyimide film, respectively, and Hf isotopic changes are caused by >0.1 wt% contamination by VACNTs. The new sample holders (VACNTs and polyimide film) are suitable for chemical classification of Hayabusa2‐return samples, because of their ease of use, applicability to multiple analytical instruments, and low contamination levels for most elements.  相似文献   
6.
7.
We observed metamorphosed clasts in the CV3 chondrite breccias Graves Nunataks 06101, Vigarano, Roberts Massif 04143, and Yamato‐86009. These clasts are coarse‐grained polymineralic rocks composed of Ca‐bearing ferroan olivine (Fa24–40, up to 0.6 wt% CaO), diopside (Fs7–12Wo44–50), plagioclase (An52–75), Cr‐spinel (Cr/[Cr + Al] = 0.4, Fe/[Fe + Mg] = 0.7), sulfide and rare grains of Fe‐Ni metal, phosphate, and Ca‐poor pyroxene (Fs24Wo4). Most clasts have triple junctions between silicate grains. The rare earth element (REE) abundances are high in diopside (REE ~3.80–13.83 × CI) and plagioclase (Eu ~12.31–14.67 × CI) but are low in olivine (REE ~0.01–1.44 × CI) and spinel (REE ~0.25–0.49 × CI). These REE abundances are different from those of metamorphosed chondrites, primitive achondrites, and achondrites, suggesting that the clasts are not fragments of these meteorites. Similar mineralogical characteristics of the clasts with those in the Mokoia and Yamato‐86009 breccias (Jogo et al. 2012 ) suggest that the clasts observed in this study would also form inside the CV3 chondrite parent body. Thermal modeling suggests that in order to reach the metamorphosed temperatures of the clasts of >800 °C, the clast parent body should have accreted by ~2.5–2.6 Ma after CAIs formation. The consistency of the accretion age of the clast parent body and the CV3 chondrule formation age suggests that the clasts and CV3 chondrites could be originated from the same parent body with a peak temperature of 800–1100 °C. If the body has a peak temperature of >1100 °C, the accretion age of the body becomes older than the CV3 chondrule formation age and multiple CV3 parent bodies are likely.  相似文献   
8.
We have experimentally determined the tracer diffusion coefficients (D*) of 44Ca and 26Mg in a natural diopside (~Di96) as function of crystallographic direction and temperature in the range of 950–1,150 °C at 1 bar and f(O2) corresponding to those of the WI buffer. The experimental data parallel to the a*, b, and c crystallographic directions show significant diffusion anisotropy in the a–c and b–c planes, with the fastest diffusion being parallel to the c axis. With the exception of logD*(26Mg) parallel to the a* axis, the experimental data conform to the empirical diffusion “compensation relation”, converging to logD ~ −19.3 m2/s and T ~ 1,155 °C. Our data do not show any change of diffusion mechanism within the temperature range of the experiments. Assuming that D* varies roughly linearly as a function of angle with respect to the c axis in the a–c plane, at least within a limited domain of ~20° from the c-axis, our data do not suggest any significant difference between D*(//c) and D*(⊥(001)), the latter being the diffusion data required to model compositional zoning in the (001) augite exsolution lamellae in natural clinopyroxenes. Since the thermodynamic mixing property of Ca and Mg is highly nonideal, calculation of chemical diffusion coefficient of Ca and Mg must take into account the effect of thermodynamic factor (TF) on diffusion coefficient. We calculate the dependence of the TF and the chemical interdiffusion coefficient, D(Ca–Mg), on composition in the diopside–clinoenstatite mixture, using the available data on mixing property in this binary system. Our D*(Ca) values parallel to the c axis are about 1–1.5 log units larger than those Dimanov et al. (1996). Incorporating the effect of TF, the D(Ca–Mg) values calculated from our data at 1,100–1,200 °C is ~0.6–0.7 log unit greater than the experimental quasibinary D((Ca–Mg + Fe)) data of Fujino et al. (1990) at 1 bar, and ~0.6 log unit smaller than that of Brady and McCallister (1983) at 25 kb, 1,150 °C, if our data are normalized to 25 kb using activation volume (~4 and ~6 cm3/mol for Mg and Ca diffusion, respectively) calculated from theoretical considerations.  相似文献   
9.
Composite P-wave seismograms are constructed for intermediate earthquakes in the Kurile region using seismic stations in central and western Japan. Ray paths are approximately parallel to the intermediate seismic zone along the Kurile-Japan arc. A compressional velocity structure model is constructed from the travel time and relative amplitude data for the upper mantle involving this intermediate seismic zone. The absence of any significant low-velocity layer below the descending slab of lithosphere can be shown from the data. Instead, the model consistent with the observed data has a non-velocity gradient layer of about 30 km thickness beneath the descending slab. The result suggests that the low-velocity layer beneath the Pacific plate thins landward across the Kurile-Japan trench and does not descend along the base of the descending slab.  相似文献   
10.
The oxygen isotopic micro-distributions within and among minerals in a coarse-grained Ca, Al-rich inclusion (CAI), 7R-19-1 from the Allende meteorite, were measured by in situ using secondary ion mass spectrometry (SIMS). All values of O isotopic ratios in 7R-19-1 minerals fall along the carbonaceous chondrite anhydrous mineral mixing (CCAM) line on a δ17OSMOW vs. δ18OSMOW plot. Major refractory minerals (spinel, fassaite and melilite) in 7R-19-1 showed large negative anomalies of Δ17O in the order, spinel (−21‰) > 16O-rich melilite (∼−18‰) > fassaite (−15 to +1‰) > 16O-poor melilite (−8 to +2‰). However, the lower limit values of Δ17O are similar at about −21‰, a value commonly observed in CAIs. The similarity in the extreme values of the isotope anomaly anomalies suggests that crystallization of all CAIs started from an 16O enrichment of 21‰ (Δ17O) relative to terrestrial values. The order of the O isotopic anomalies observed for 7R-19-1, except for 16O-poor melilite, is parallel to the crystallization sequence determined by experiment from CAI liquid (Stolper, 1982), indicating that the O isotopic exchange in 7R-19-1 occurred between CAI melt and surrounding gas while 7R-19-1 was crystallizing from the 16O enriched CAI liquid (∼−21‰ in Δ17O) in the 16O-poor solar nebula. However, the a single crystallization sequence during the cooling stage cannot explain the existence of 16O-poor melilite. The presence of 16O-poor melilite suggests that multiple heating events occurred during CAI formation. The sharp contact between 16O-rich and 16O-poor melilite crystals and within 16O-rich melilite indicates that these multiple heatings occurred quickly. Based on the O isotopic and chemical compositions, fassaite crystals were aggregates of relic crystals formed from CAI melt whichthat have had various O isotopic compositions from the remelting processes. The results of intra-mineral distributions of O isotopes also support multiple heating events during CAI formation.  相似文献   
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