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221.
New insights into the origin of perylene in geological samples   总被引:1,自引:0,他引:1  
The origin of the polycyclic aromatic hydrocarbon (PAH) perylene in sediments and petroleum has been a matter of continued debate. Reported to occur in Phanerozoic organic matter (OM), fossil crinoids and tropical termite mounds, its mechanism of formation remains unclear. While a combustion source can be excluded, structural similarities to perylene quinone-like components present in e.g. fungi, plants, crinoids and insects, potentially suggest a product-precursor relationship. Here, we report perylene concentrations, 13C/12C, and D/H ratios from a Holocene sediment profile from the Qingpu trench, Yangtze Delta region, China. Perylene concentrations differ from those of pyrogenic PAHs, and rise to prominence in a stratigraphic interval that was dominated by woody vegetation as determined by palynology including fungal spores. In this zone, perylene concentrations exhibit an inverse relationship to the lignin marker guaiacol, D/H ratios between −284‰ and −317‰, similar to the methoxy groups in lignin, as well as co-variation with spores from wood-degrading fungi. 13C/12C of perylene differs from that of land plant wax alkanes and falls in the fractionation range expected for saprophytic fungi that utilise lignin, which is isotopically lighter than cellulose and whole wood. During progressive lignin degradation, the relative carbon isotopic ratio of the perylene decreases. We therefore hypothesise a relationship of perylene to the activity of wood-degrading fungi. To support our hypothesis, we analysed a wide range of Phanerozoic sediments and oils, and found perylene to generally be present in subordinate amounts before the evolutionary rise of vascular plants, and to be generally absent from marine-sourced oils, few exceptions being attributed perhaps to a contribution of marine and/or terrestrial-derived fungi, anoxia (especially under marine conditions) and/or contamination of core material by fungi. A series of low-molecular-weight aromatic quinones bearing the perylene-backbone were detected in Devonian and Cretaceous sediments, potentially representing precursor components to perylene.  相似文献   
222.
Abstract Thickness variations across‐levee and downchannel in acoustically defined depositional sequences from six submarine channel‐levee systems show consistent and quantifiable patterns. The thickness of depositional sequences perpendicular to the channel trend, i.e. across the levee, decreases exponentially, as characterized by a spatial decay constant, k. Similarly, the thickness of sediment at the levee crest decreases exponentially down the upper reaches of submarine channels and can be characterized by a second spatial decay constant, λ. The inverse of these decay constants has units of length and defines depositional length scales such that k?1 is a measure of levee width and λ?1 is a measure of levee length. Quantification of levee architecture in this way allowed investigation of relationships between levee architecture and channel dimensions. It was found that these measures of levee e‐folding width and levee e‐folding length are directly related to channel width and relief. The dimensions of channels and levees are thus intimately related, thereby limiting the range of potential channel‐levee morphologies, regardless of allocyclic forcing. A simple sediment budget model relates the product of the levee e‐folding width and e‐folding length to through‐channel volume discharge. A classification system based on the quantitative downchannel behaviour of levee architecture allows identification of a ‘mid‐channel’ reach, where sediment is passively transferred from the through‐channel flow to the levees as an overspilling flow. Downstream from this reach, the channel gradually looses its control on guiding turbidity currents, and the resulting flow can be considered as an unconfined or spreading flow.  相似文献   
223.
Coesite was discovered as inclusions in zircon separates from pelitic gneiss associated with a large eclogite body in the North Qaidam ultrahigh-pressure (UHP) terrane. Some graphite inclusions were also found. This finding suggested the occurrence of in-situ UHP metamorphism and that the terrane was most likely recrystallized at pressures below the diamond stability field. It supported other previous indirect UHP evidence, such as polycrystalline quartz inclusions in eclogitic garnet, quartz lamellae in omphacite and P-T estimates for both eclogite and garnet peridotite. The U-Pb and Sm-Nd ages of the North Qaidam eclogite indicated that subduction of continental crust occurred in the Early Palaeozoic, which probably recorded a collision between the Sino-Korean and Yangtze plates.  相似文献   
224.
The Valhalla uranium deposit, located 40 km north of Mount Isa, Queensland, Australia, is an albitite-hosted, Mesoproterozoic U deposit similar to albitite-hosted uranium deposits in the Ukraine, Sweden, Brazil and Guyana. Uranium mineralisation is hosted by a thick package of interbedded fine-grained sandstones, arkoses and gritty siltstones that are bound by metabasalts belonging to the ca. 1,780 Ma Eastern Creek Volcanics in the Western Succession of the Mount Isa basin. Alteration associated with U mineralisation can be divided into an early, main and late stage. The early stage is dominated by laminated and intensely altered rock comprising albite, reibeckite, calcite, (titano)magnetite ± brannerite. The main stage of mineralisation is dominated by brecciated and intensely altered rocks that comprise laminated and intensely altered rock cemented by brannerite, apatite, (uranoan)-zircon, uraninite, anatase, albite, reibeckite, calcite and hematite. The late stage of mineralisation comprises uraninite, red hematite, dolomite, calcite, chlorite, quartz and Pb-, Fe-, Cu-sulfides. Brannerite has U–Pb and Pb–Pb ages that indicate formation between 1,555 and 1,510 Ma, with significant Pb loss evident at ca. 1,200 Ma, coincident with the assemblage of Rodinia. The oldest ages of the brannerite overlap with 40Ar/39Ar ages of 1,533 ± 9 Ma and 1,551 ± 7 Ma from early and main-stage reibeckite and are interpreted to represent the timing of formation of the deposit. These ages coincide with the timing of peak metamorphism in the Mount Isa area during the Isan Orogeny. Lithogeochemical assessment of whole rock data that includes mineralised and unmineralised samples from the greater Mount Isa district reveals that mineralisation involved the removal of K, Ba and Si and the addition of Na, Ca, U, V, Zr, P, Sr, F and Y. U/Th ratios indicate that the ore-forming fluid was oxidised, whereas the crystal chemistry of apatite and reibeckite within the ore zone suggests that F and were important ore-transporting complexes. δ18O values of co-existing calcite and reibeckite indicate that mineralisation occurred between 340 and 380°C and involved a fluid having δ18Ofluid values between 6.5 and 8.6‰. Reibeckite δD values reveal that the ore fluid had a δDfluid value between −98 and −54‰. The mineral assemblages associated with early and main stages of alteration, plus δ18Ofluid and δDfluid values, and timing of the U mineralisation are all very similar to those associated with Na–Ca alteration in the Eastern Succession of the Mount Isa basin, where a magmatic fluid is favoured for this style of alteration. However, isotopic data from Valhalla is also consistent with that from the nearby Mount Isa Cu deposit where a basinal brine is proposed for the transport of metals to the deposit. Based on the evidence to hand, the source fluids could have been derived from either or both the metasediments that underlie the Eastern Creek Volcanics or magmatism that is manifest in the Mount Isa area as small pegmatite dykes that intruded during the Isan Orogeny.  相似文献   
225.
新疆准噶尔盆地北部中-新生代地层分布广,化石类型多样,成为古生物、古气候、古环境研究理想地区.乌伦古河组和依希白拉组分别发现恐龙与哺乳动物等脊椎动物化石,证实它们不存在混生现象,对恐龙是否延续至新生代提出初步意见.  相似文献   
226.
The behaviour of subaerial particle-laden gravity currents (e.g. pyroclastic flows, lahars, debris flows, sediment-bearing floods and jökulhlaups) flowing into the sea has been simulated with analogue experiments. Flows of either saline solution, simple suspensions of silicon carbide (SiC) in water or complex suspensions of SiC and plastic particles in methanol were released down a slope into a tank of water. The excess momentum between subaerial and subaqueous flow is dissipated by a surface wave. At relatively low density contrasts between the tank water and the saline or simple suspensions, the flow mixture enters the water and forms a turbulent cloud involving extensive entrainment of water. The cloud then collapses gravitationally to form an underwater gravity current, which progresses along the tank floor. At higher density contrasts, the subaerial flow develops directly into a subaqueous flow. The flow slows and thickens in response to the reduced density contrast, which is driving motion, and then continues in the typical gravity current manner. Complex suspensions become dense flows along the tank floor or buoyant flows along the water surface, if the mixtures are sufficiently denser or lighter than water respectively. Flows of initially intermediate density are strongly influenced by the internal stratification of the subaerial flow. Material from the particulate-depleted upper sections of the subaerial flow becomes a buoyant gravity current along the water surface, whereas material from the particulate-enriched lower sections forms a dense flow along the tank floor. Sedimentation from the dense flow results in a reduction in bulk density until the mixture attains buoyancy, lifts off and becomes a secondary buoyant flow along the water surface. Jökulhlaups, lahars and debris flows are typically much denser than seawater and, thus, will usually form dense flows along the seabed. After sufficient sedimentation, the freshwater particulate mixture can lift off to form a buoyant flow at the sea surface, leading to a decoupling of the fine and coarse particles. Flood waters with low particulate concentrations (<2%) may form buoyant flows immediately upon entering the ocean. Subaerial pyroclastic flows develop a pronounced internal stratification during subaerial run-out and, thus, a flow-splitting behaviour is probable, which agrees with evidence for sea surface and underwater flows from historic eruptions of Krakatau and Mont Pelée. A pyroclastic flow with a bulk density closer to that of sea water may form a turbulent cloud, resulting in the deposition of much of the pyroclasts close to the shore. Dense subaqueous pyroclastic flows will eventually lift off and form secondary buoyant flows, either before or after the transformation to a water-supported nature.  相似文献   
227.
The leaching of coal and coal/asphaltite/wood-ashes in sulfuric acid (pH 1.0, 25 °C, S/L, 1:10) was studied as a function of time; acid consumption and extracted metal concentrations are presented. Whole coals consumed acid rapidly during the first few minutes, followed by slow acid consumption. Wood-, lignite-, and asphaltite-ashes consumed acid in two stages, the rapid phase extending < 30 min and the slow phase extended up to 10 days. The rapid phase was dominated by the dissolution of Ca, K and Mg ions for wood-ash, by Ca, Al and Mg ions for lignite-ash and Ca and Mg ions for asphaltite-ash. The sulfur concentration in solution and the concentrations of Ca, Fe, K, Mg, Na, P, Al and Mn in the aqueous phase verified the neutralizing capacity of the untreated ashes as well as the formation of insoluble sulfates in the residues. The slow phase kinetics differed for different fuels and exhibited leaching of several abundant elements—Fe, Al, K, Na and Mn. Trace elements (Ba, Cd, Co, Cr, Cu, Mo, Ni, Pb, Th, U, V, Zn) sometimes required up to 32 h for maximal extraction from ashes. Suggestions are presented regarding the chemical nature of trace elements in the untreated coals and ashes and suitable residence times for economical industrial processes. We think it possible to combine bacteriological oxidation of sulfidic concentrates of acid leaching from ash of various qualities or even whole coals.  相似文献   
228.
Compositions of chrome-spinels in peridotites from the layered igneous rocks of Rhum and of the Ben Buie intrusion, Mull, show evidence of post-depositional reaction relationships with the cumulus olivine and/or the intercumulus liquid. Some seam-forming spinels in the Ben Buie intrusion are highly aluminous, more so than those in the Rhum intrusion. Occasional zoned spinels, in both intrusions, show enrichment in Al towards their rims. The evidence suggests that the spinel reaction trend involving Cr-Al exchange proceeds in the direction of Al-enrichment. Equilibrium between chrome-spinel and cumulus olivine appears to have been attained rarely, thus limiting the application of the olivine-spinel geothermometer.  相似文献   
229.
Industrial decentralisation (ID) has been a central component of South Africa's regional strategy for over twenty years. Until recently, though, the programme has evinced little interest amongst industrialists. The fact that ID policy has been premised upon political rather than economic considerations has been thought to lie at the root of this failure. Following recent developments, however, this view is being reassessed. The reorganisation of ID policy in 1982 and the dramatic acceleration in the rate of industrial relocations that this reorganisation appears to have induced, has led theorists to revise their thinking on both the economic and political imperatives underpinning the programme. The purpose of this paper is to review the debates that are now developing concerning ID in South Africa, and to suggest where further research and analysis might be most profitably directed.  相似文献   
230.
The distribution of macroinvertebrates on Connecticut tidal marshes corresponds well with that reported for other marshes along the Atlantic and Gulf coasts of the United States. The greatest densities and biomass of the ribbed mussel,Geukensia demissa, were found on marshes in the central and western part of the state where both the annual production ofSpartina alterniflora and tidal range are large. *** DIRECT SUPPORT *** A01BY019 00011  相似文献   
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