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1.
The nature of Re-platinum-group element (PGE; Pt, Pd, Ir, Os, Ru) transport in the marine environment was investigated by means of marine sediments at and across the Cretaceous-Tertiary boundary (KTB) at two hemipelagic sites in Europe and two pelagic sites in the North and South Pacific. A traverse across the KTB in the South Pacific pelagic clay core found elevated levels of Re, Pt, Ir, Os, and Ru, each of which is approximately symmetrically distributed over a distance of ∼1.8 m across the KTB. The Re-PGE abundance patterns are fractionated from chondritic relative abundances: Ru, Pt, Pd, and Re contents are slightly subchondritic relative to Ir, and Os is depleted by ∼95% relative to chondritic Ir proportions. A similar depletion in Os (∼90%) was found in a sample of the pelagic KTB in the North Pacific, but it is enriched in Ru, Pt, Pd, and Re relative to Ir. The two hemipelagic KTB clays have near-chondritic abundance patterns. The ∼1.8-m-wide Re-PGE peak in the pelagic South Pacific section cannot be reconciled with the fallout of a single impactor, indicating that postdepositional redistribution has occurred. The elemental profiles appear to fit diffusion profiles, although bioturbation could have also played a role. If diffusion had occurred over ∼65 Ma, the effective diffusivities are ∼10−13 cm2/s, much smaller than that of soluble cations in pore waters (∼10−6 cm2/s). The coupling of Re and the PGEs during redistribution indicates that postdepositional processes did not significantly fractionate their relative abundances. If redistribution was caused by diffusion, then the effective diffusivities are the same. Fractionation of Os from Ir during the KTB interval must therefore have occurred during aqueous transport in the marine environment. Distinctly subchondritic Os/Ir ratios throughout the Cenozoic in the South Pacific core further suggest that fractionation of Os from Ir in the marine environment is a general process throughout geologic time because most of the inputs of Os and Ir into the ocean have Os/Ir ratios ≥1. Mass balance calculations show that Os and Re burial fluxes in pelagic sediments account for only a small fraction of the riverine Os (<10%) and Re (<0.1%) inputs into the oceans. In contrast, burial of Ir in pelagic sediments is similar to the riverine Ir input, indicating that pelagic sediments are a much larger repository for Ir than for Os and Re. If all of the missing Os and Re is assumed to reside in anoxic sediments in oceanic margins, the calculated burial fluxes in anoxic sediments are similar to observed burial fluxes. However, putting all of the missing Os and Re into estuarine sediments would require high concentrations to balance the riverine input and would also fail to explain the depletion of Os at pelagic KTB sites, where at most ∼25% of the K-T impactor’s Os could have passed through estuaries. If Os is preferentially sequestered in anoxic marine environments, it follows that the Os/Ir ratio of pelagic sediments should be sensitive to changes in the rates of anoxic sediment deposition. There is thus a clear fractionation of Os and Re from Ir in precipitation out of sea water in pelagic sections. Accordingly, it is inferred here that Re and Os are removed from sea water in anoxic marine depositional regimes.  相似文献   
2.
This study explores the possibility of establishing Nd isotopic variations in seawater over geologic time. Calcite, aragonite and apatite are examined as possible phases recording seawater values of ?Nd. Modern, biogenic and inorganically precipitated calcite and aragonite from marine environments were found to have Nd concentrations of from 0.2 to 70 ppb, showing that primary marine CaCO3 contains little REE and that Nd/Ca is not greatly enhanced relative to seawater during carbonate precipitation. Very young marine limestone and dolomite containing no continental detritus have ~200 ppb Nd. All the carbonates are LREE enriched (?0.16 ≤fSmNd≤?0.45). Modern and very young Atlantic and Pacific carbonates have ?Nd in the range of shallow Atlantic and Pacific seawater respectively, implying that they derive their REE from local seawater. The Nd in well preserved carbonate fossils is ≤4 × 104 ppb, much greater than in their modern counterparts but like the high values found for carbonates in other studies. We believe the high REE contents (at the 500 ppb level) in some detritusfree carbonates are due to REE-rich Fe-hydroxide in/on the carbonate. In favorable cases, such material may record seawater ?Nd values, however introduction of extraneous REE may obscure the original isotopic composition of pure CaCO3 because of its very low intrinsic primary REE abundance.Modern biogenic apatite is also shown to have very low REE content (<150 ppb Nd) but appears to quickly scavenge REE from seawater. Inorganically precipitated apatite from phosphorites has high concentrations of seawater-derived REE. Young phosphorite apatite from the Atlantic and Pacific oceans has ?Nd in the range of the seawater from these oceans. Older apatite samples of similar age from different localities bordering common oceans record similar values of ?Nd(T). Sedimentary apatite has ?Sr(T) values in good agreement with the curves for 87Sr86Sr of seawater as a function of time. Individual conodonts from a single formation yield the same ?Sr(T) and ?Nd(T). Other workers have shown that sedimentary apatite preserves seawater REE patterns. These characteristics suggest that sedimentary apatite can be used to determine ?Nd(T) in ancient seawater. The seawater values so inferred range between ?1.7 and ?8.9 over the last 700 my and lie in the range of modern seawater, showing no evidence for drastic changes. High values of seawater ?Nd(T) in the Triassic and latest Precambrian may correlate with the breakup of large continental landmasses. The initial ?Nd(T) =?15.0 of a 2 AE old phosphorite implies the presence of ~ 1.5 AE old continental crust at 2 AE ago. The approach outlined here can be used to constrain the age of the exposed crust as a function of time.  相似文献   
3.
The absolute isotope abundance of Ti has been determined in Ca-Al-rich inclusions from the Allende and Leoville meteorites and in samples of whole meteorites. The absolute Ti isotope abundances differ by a significant mass dependent isotope fractionation transformation from the previously reported abundances, which were normalized for fractionation using 46Ti48Ti. Therefore, the absolute compositions define distinct nucleosynthetic components from those previously identified or reflect the existence of significant mass dependent isotope fractionation in nature. We provide a general formalism for determining the possible isotope compositions of the exotic Ti from the measured composition, for different values of isotope fractionation in nature and for different mixing ratios of the exotic and normal components. The absolute Ti and Ca isotopic compositions still support the correlation of 50Ti and 48Ca effects in the FUN inclusions and imply contributions from neutron-rich equilibrium or quasi-equilibrium nucleosynthesis. The present identification of endemic effects at 46Ti, for the absolute composition, implies a shortfall of an explosive-oxygen component or reflects significant isotope fractionation. Additional nucleosynthetic components are required by 47Ti and 49Ti effects. Components are also defined in which 48Ti is enhanced.Bulk samples of carbonaceous meteorites (C2 and C3 types) show distinct excesses at 50Ti but no nonlinear effects at the other Ti isotopes. Other chondrites, including Orgueil (Cl), show no nonlinear effects. Relative to terrestrial Ti, a small isotope fractionation is found for only an enstatite chondrite. The Ti absolute compositions in Ca-Al-rich inclusions show significant isotope fractionation effects corresponding to an enhancement in the heavier isotopes relative to the lighter isotopes as compared to Ti in a TiO2 standard and in chondrites. The absence of a correlation of Ti isotope fractionation effects with those for Ca and Mg is indicative of multiple processes of condensation, volatilization and recondensation; however, the mechanisms causing the isotope fractionation are not well understood.  相似文献   
4.
5.
Field evidence indicates that the Trinity peridotite was partially melted during its rise as a part of the upwelling convecting mantle at a spreading center. A SmNd mineral isochron for a plagioclase lherzolite yields an age,T = 427 ± 32 Ma and initialεNd = + 10.4 ? 0.4 which is distinctly higher than that expected for typical depleted mantle at this time. This age is interpreted as the time of crystallization of trapped melt in the plagioclase lherzoliteP-T field. This time of crystallization probably represents the time when the massif was incorporated as a part of the oceanic lithosphere. The SmNd model age of the plagioclase lherzolite totalrock isTCHURNd = 3.4 AE. This suggests that the Trinity peridotite was derived from a mantle that was depleted rather early in earth history. The peridotite contains many generations of pyroxenite dikes and some microgabbro dikes. We report data for two dikes that clearly crosscut the main metamorphic fabric of the peridotite. A microgabbro dike yields a SmNd mineral isochron age ofT = 435 ± 21 Ma andεNd = + 6.7 ? 0.3. A pyroxenite dike yields an initialεNd = + 7.3 ± 0.4. The initialεNd values for the pyroxenite and gabbro dikes are fairly similar to those for the depleted mantle at this time and are distinct from the lherzolite—demonstrating that they are not genetically related. RbSr data do not give any coherent pattern. However, some bounds can be put on initial Sr values ofεSr ? ?21 for the plagioclase lherzolite andεSr ? ?8.7 for the microgabbro dike. It is plausible that the dikes represent cumulates left behind from island arc magmas that rose through the the oceanic lithosphere within the vicinity of a subduction zone. Major and trace elements and SmNd isotopic data indicate a multiple stage history for the Trinity peridotite; a small melt fraction was extracted from an undepleted source ~ 3.4 AE or more ago to produce the proto-lherzolite; a large fraction of melt (~ 12 to 23%) was extracted from the proto-lherzolite to produce the present rock; the lherzolite was then crosscut by dikes from average depleted mantle ~ 0.44 AE ago. The data are compatible with the depleted mantle source being formed very early in earth history. Although most available data indicate that the depleted upper mantle has been relatively well stirred through time, the Trinity data suggest that very ancient Nd isotopic values are preserved and thus chemical and physical heteorgeneities are sometimes preserved in the depleted source of mid-ocean ridge basalts as well as the oceanic lithosphere which they intrude.  相似文献   
6.
7.
Ar analyses are reported for five coarse-grained, Ca-Al-rich inclusions from the Allende meteorite. The samples were neutron-irradiated in individual evacuated ampoules, and the Ar gas in the ampoules as well as the samples was analyzed. A large fraction (up to 60%) of the39Ar from39K (n, p) reactions was lost out of the inclusions into the ampoules. The39Ar losses resulted in substantial increases in the apparent40Ar-39Ar ages of the samples.39Ar recoil loss during neutron-irradiation is a major effect and must be accounted for in40Ar-39Ar dating. All of the Allende inclusions studied contained substantial trapped36Ar. The origin of the trapped36Ar is unknown, and the possible presence of trapped40Ar cannot be excluded. Ar measurements on Allende inclusions which have yielded anomalously old ages must be re-examined in the context of39Ar recoil loss and possible contributions of trapped40Ar. Allende inclusions appear on both accounts to be poor candidates to search for relicts of presolar materials with well-defined K/Ar ages.  相似文献   
8.
The isotopic composition of Ag and the concentration of Ag and Pd have been determined in Canyon Diablo (IA), Grant (IIIB), Hoba, Santa Clara, Tlacotepec and Warburton Range (IVB), Piñon and Deep Springs (anom.). Troilite from Grant and Santa Clara have also been analyzed. All of these meteorites, with the exception of Canyon Diablo, give 107Ag109Ag in the metal phase that is greater than the terrestrial value with the enrichments of 107Ag ranging from ~2% to 212%. These data show that Ag of anomalous isotopic composition is common to all IVB and anomalous meteorites. The results on Grant suggest that the anomalies may be widespread including more common meteorite groups. There is a general correlation of 107Ag109Ag with PdAg except for the data from FeS of Santa Clara. It is concluded that the excess 107Ag is the result of decay of 107Pd, a nuclide that is extinct at present with an abundance of 107Pd108Pd of about 3 × 10?5. The troilite in Grant exhibits normal 107Ag109Ag to within errors, a high Ag concentration and a low ratio of 108Pd109Ag ~0.17. Grant metal has 107Ag109Ag that is ~2% greater than normal and a high ratio of 108Pd109Ag ~ 103. The data from Grant appear to represent a 107Pd-107Ag isochron and indicate that the cooling rate at elevated temperatures was sufficiently rapid to preserve substantial isotopic differences between metal and troilite. Troilite in Santa Clara was found to contain Ag with a very high 107Ag109Ag ratio (108% above normal), an Ag concentration only a factor of three above the metal and a high value of 108Pd109Ag ~1.3 × 104. The troilite has a higher 107Ag109Ag than the metal. These data are not compatible with a simple model of in situ decay and subsequent local Ag redistribution between metal and troilite during cooling. These data suggest that Ag in Santa Clara and possibly other IVB meteorites is made up of almost pure 107Ag produced from 107Pd decay and 109Ag produced by nuclear reactions with only a small amount of “normal” Ag. This indicates an intense energetic particle bombardment history in the early solar system (~1020 p/m2) which occurred after the formation of small planetary bodies. We infer that a T-Tauri activity by the early sun contributed to some late stage “nucleosynthesis” and the heating of a dust cloud. In addition, implications on the early thermal evolution of iron meteorites are presented based on 107Pd decay and models of the cooling history.  相似文献   
9.
Luna 16 sample B-1 was the largest fragment (62 mg) obtained in the sample exchange with the USSR. Petrologic, mineralogic, and chemical investigations have been made on this fragment in conjunction with Rb-Sr and40Ar/39Ar investigations by our colleagues. Sample B-1 is a fine-grained ophitic basalt but is distinguished from the Apollo samples by containing a single pyroxene, predominantly pigeonitic, an ilmenite content (7%) intermediate to that of the Apollo 11 and 12 samples, and subequal amounts of pyroxene (50%) and plagioclase (40%). Chemically it is distinguished by a high Sr content (437 ppm) and a high K/U value (4700). The K-content (1396 ppm) is higher than that of Luna 16 soil sample A-2.  相似文献   
10.
Ages were determined by the 40Ar-39Ar method on two metaclastic rocks returned from the lunar highlands north of Mare Fecunditatis by the Luna 20 probe. Both samples gave very well-defined argon retention ages of 3.90 ± 0.04 AE which are indistinguishable from each other within a resolution of 0.02 AE. Both fragments, 22006 and 22007, are highly recrystallized polymict breccias; there is no evidence for loss of radiogenic 40Ar, and the age almost surely dates the time of recrystallization. The cosmic ray exposure ages of these fragments are similar and high: 900 million years for 22006, 1300 million years for 22007. 22007 also contains substantial trapped argon with a high 40Ar36Ar ratio.The Luna 20 results greatly extend the area of the Moon's surface exhibiting a well-defined record of metamorphism at 3.9 AE. So far, lunar history in the interval 4.6?3.9 AE is not preserved in the ages of surface rocks. This obliteration suggests lunar-wide metamorphic conditions occurring or terminating at this time as a result of major impacts.  相似文献   
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