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851.
Charophytes are very common in Australian modern and Quaternary waterbodies, and are quite commonly incorrectly reported as “Chara” sp. or Lamprothamnium papulosum (Wallroth) Groves. This paper is the first attempt at the identification of the widespread euryhaline genus Lamprothamnium in Australia, and its use as a paleoenvironmental indicator. Lamprothamnium is distributed worldwide in all continents, except north and central America. The Australian environment, characterized by increasing aridity during the last 500 ka, has an abundance of saline lakes. We sampled 30 modern lakes and identified extant Lamprothamnium macropogon (A. Braun) Ophel and Lamprothamnium succinctum (A. Braun in Ascherson) Wood. Fossil gyrogonites, from lacustrine sediments ∼65 ka old from Madigan Gulf, Lake Eyre, were identified as Lamprothamnium williamsii sp. nov. We applied statistical analysis (analysis of variance, ANOVA) to the morphometry of the gyrogonites from one fossil and three living Lamprothamnium populations. The ANOVA test suggests all the populations are different, including two separate populations of extant L. macropogon, interpreted in this case as the expression of ecophenotypic variability. Lamprothamnium is a useful paleoenvironmental indicator because it indicates a non-marine environment with varying salinity ranging from fresh (usually 2–3 g l−1) to 70 g l−1, and water bodies holding water for at least 70 consecutive days. Collectively, these parameters provide important information in the study of ephemeral habitats.  相似文献   
852.
Major- and trace-element compositions of zircons and whole rocks from 14 barren and seven ore-bearing calc-alkaline intrusions from the Chuquicamata-El Abra porphyry copper belt of northern Chile have been measured in situ by excimer laser ablation (ELA) ICP-MS. These data permit the Ce(IV)/Ce(III) ratio within zircon to be calculated using a lattice-strain model for mineral-melt partitioning of Ce(IV) and Ce(III). Zircon Ce(IV)/Ce(III) and EuN/EuN* ratios, and by inference magmatic oxidation states, generally increase from older, mafic to younger, felsic units. Within this sequence, porphyry copper mineralization is directly associated only with intrusions with zircon Ce(IV)/Ce(III)>300 and EuN/EuN*>0.4. Such trends can be understood in terms of interdependent relations between oxygen fugacity, sulfur speciation and solubility, and chalcophile element partitioning in silicate magmas. Because zircon occurs in most calc-alkaline intrusions and is resistant to subsolidus alteration, zircon Ce(IV)/Ce(III) ratios provide a useful tool for evaluating the economic potential of such rocks for magmatic-hydrothermal Cu-Au mineralization. The approach is general and may provide a means to infer relative oxidation state in a wide range of intermediate to felsic igneous rocks.  相似文献   
853.
Large-scale column experiments were undertaken to evaluate the potential of polymer mats to remove selected volatile organic compounds, polycyclic aromatic hydrocarbons, and pesticides (atrazine and fenamiphos) from ground water and potentially to act as permeable reactive barriers in contaminated ground water environments. The polymer mats, composed of interwoven silicone (dimethylsiloxane) tubes and purged with air, were installed in 2 m long flow-through columns. The polymer mats proved efficient in physically removing (stripping) benzene and naphthalene from contaminated water. Removal efficiencies for both these compounds from an aqueous phase flowing past a polymer mat were 75% or greater. However, for atrazine and fenamiphos, removal efficiencies were 5% or less, probably as a result of their lower Henry's law constants and possibly lower polymer diffusion coefficients.
These experiments indicate that, at least for relatively volatile compounds, polymer mats can provide a remediation technique for the removal of organic compounds from contaminated water. Application of this technique may be well suited as a longer-term, semipassive strategy to remediate contaminated ground water, using natural ground water flow to deliver contaminated ground water to polymer mats engineered as sorption-stripping barriers.
Additional benefits of this technique may include targeted delivery of gaseous chemical amendments, such as oxygen, to enhance aerobic biodegradation and to further reduce any residual concentrations of contaminants.  相似文献   
854.
855.
Hydrothermally altered andesites in the upper member of the Amulet formation at Buttercup Hill, Noranda, Quebec represent part of the aquifer and cap of a self-sealing geothermal system that focussed the discharge of hydrothermal fluids during the formation of massive Cu-Zn sulfide deposits. Five alteration facies are recognized

1. 1) pervasive greenschist faciés regional metamorphism (least-altered andesite)

2. 2) epidotization-silicification

3. 3) albitization-silicification

4. 4) chloritization

5. 5) sericitization-silicification. Alteration is localized on permeable zones such as amygdules, fractures, flow tops, discordant breccia dikes, and conformable breccia horizons.

Epidotized-silicified andesite is enriched in Ca-Sr-Eu and depleted in Mg and first transition series metals (FTSM) relative to least-altered andesite. Albitized-silicified andesite is significantly enriched in Na and depleted in most FTSM relative to least-altered andesite. The abundances and inter-element ratios of the rare-earth elements (REE) and most high field-strength elements (HFS: Y, Zr, Th, U, Hf, Ta) are similar in least-altered, epidotized-silicified and albitized-silicified andesites. The most silicified andesites are strongly enriched in Na-Si, strongly depleted in Mg and divalent FTSM and slightly but systematically depleted in REE and most HFS elements. Serialized andesites were previously silicified; they are very strongly enriched in K-Rb-Cs-Ba, very strongly depleted in Na-Ca-Sr-Eu and slightly depleted in light REE relative to silicified andesite. Chloritized andesitic rocks exhibit heavy REE and HFS element ratios similar to those of leastaltered andesite, but are relatively strongly enriched in Mg and divalent FTSM, strongly depleted in Si and large ion lithophile (LIL) elements and slightly depleted in light REE.

The coupled behavior of the heavy REE and most HFS elements during epidotization, albitization, silicification, chloritization and serialization suggests that they were inert during hydrothermal modification of the andesite. Mass balance calculations suggest that volume was conserved during epidotization-silicification and albitization-silicification, but that intense silicification was accompanied by volume increases up to 30 percent.  相似文献   

856.
857.
Constant-temperature laboratory culture experiments of the planktonic foraminiferal species Globigerinoides sacculifer (Brady) suggest that the ratios of Li and Sr to Ca in the shells are a function of these ratios in the culture solutions. MgCa and NaCa in the shells did not vary with changes of these ratios in the culture solution. These are the first direct determinations of the relationship between foraminiferal shell chemistry and solution composition.The possibility of temperature dependence for the minor elemental composition of foraminiferal shells was also investigated in the laboratory and by analysis of several planktonic and one benthic foraminiferal species from sediment trap and sediment core samples. The SrCa, MgCa, and NaCa ratios in the natural samples roughly correlate with calcification temperature, whereas differences in the Li/Ca ratios are small and not systematically related to temperature. However, laboratory culture experiments at 20°C and 30°C showed no variation in the LiCa, SrCa, MgCa, and NaCa ratios with calcification temperature for the planktonic foraminifera G. sacculifer and Orbulina universa. Therefore, observed differences in the SrCa, MgCa, and NaCa ratios for the sediment trap and core foraminiferal samples cannot be ascribed to direct effects of calcification temperature, but may be due to some other environmental factor which is correlated with temperature.  相似文献   
858.
Thin (0.5–4 mm), contorted stringers of talc, associated with apatite and minor pyrite, are containdy Formation in eastern Alabama. The form, position and lithologic distribed within generally saccharoidal dolomite-quartz marbles of the Cambrian Shaution of the stringers strongly suggest an algalstromatolitic origin, with interlaminar trapped dolomitic muds. Metamorphic formation of talc plus apatite proceeded only within the stringers, whereas surrounding marble remained as unreacted dolomite plus quartz. Talc generation is best explained by the reaction $${\text{dolomite}} + {\text{silica}} + {\text{water}} + {\text{P}}_{\text{2}} {\text{O}}_{\text{5}} = {\text{talc}} + {\text{apatite}} + {\text{CO}}_{\text{2}}$$ in which the phosphate was supplied to the reaction from organic matter contained within the stromatolitic layers. The system was probably open to CO2 during metamorphism, and \(P_{{\text{CO}}_{\text{2}} }\) remained relatively low.  相似文献   
859.
860.
A seasonal reconstruction of the Indian Ocean during the last glacial maximum (18,000 yr B.P.) reveals that its surface circulation and sea surface temperature patterns were significantly different from the modern Indian Ocean. This reconstruction is based on the planktonic foraminiferal biogeography and estimated sea surface temperatures in 42 Indian Ocean samples. Compared to modern conditions, the polar front was 5° to 10° latitude further north during the last glacial maximum; the Subtropical Convergence was 2° to 5° latitude further north. The West Australian Current was more intense as part of the West Wind Drift was deflected northward along the coast of Australia. The Agulhas Current was cooler and weaker during the summer and more saline and subtropical during the winter. In general, the low latitudes underwent little temperature change. The western Arabian Sea was warmer which implies less upwelling and a weaker Southwest Monsoon. On the average, the Indian Ocean was 1.9°C cooler in February and 1.7°C cooler in August during the last glacial maximum.  相似文献   
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