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101.
In Sconser quarry, Isle of Skye, a thin Tertiary basic sill is cut by vertical veins which formed fluid conduits in a major meteoric-hydrothermal system. In order to study the relative mobility of different elements during hydrothermal metamorphism, sill material adjacent to a large (6 mm wide) vein was cut into slices and subjected to geochemical and isotopic analysis. Isotopic evidence indicates that the basic magma which formed the sill was contaminated by Lewisian (Archaean) gneisses at depth, while material from Torridonian (Proterozoic) sandstone country rocks was introduced by hydrothermal fluids after crystallisation. The behaviour of the different elements during hydrothermal metamorphism divides them into 4 groups.
  1. Large-ion low-charge elements Ba, K, Rb and Cs were strongly leached from the wall rock in the vicinity of the vein.
  2. Other elements including Sr and Pb were depleted near the vein, but isotopic evidence indicates addition of some material from the fluids. This two-way nuclide transport forms an exchange process.
  3. Many high-field-strength elements including the REE are slightly enriched near the vein, but Nd isotope evidence reveals no addition of material from fluids. These elements must have been relatively enriched by the removal of other elements (mainly Si and Al).
  4. Ca and Na were added to the wall rock from fluid. The variable mobility of these elements is explained by the differing ease with which they could be incorporated into a new albite-calcite-chlorite-epidote mineralogy. The constitution of this hydrothermal mineralogy was largely determined by the primary igneous mineralogy, though the composition of hydrothermal fluids had a subordinate influence.
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102.
We have investigated the partitioning of Ir. Ge, Ga, W, Cr, Au, P, and Ni between solid metal and metallic liquid as a function of temperature and S-concentration of the metallic liquid. Partition coefficients for siderophile elements such as Ir, W, Ga and Ge increase by factors of 10–100 as the Sconcentration of the metallic liquid increases from 0–30 wt%. Partition coefficients for other siderophile elements such as Ni, Au and P increase by only factors of 2–3. In contrast, partition coefficients for the more chalcophile element Cr decrease. These experimentally-determined partition coefficients have been used in conjunction with a fractional crystallization model to reproduce the geochemical behavior of Ni, P, Au and Ir during the magmatic evolution of groups IIAB, IIIAB, IVA and IVB iron meteorites. The mean S-concentration for each group increases in the order IVB, IVA, IIIAB, IIAB, in accord with cosmochemical prediction. However, we are unable to reproduce the geochemical behavior of Ge, Ga, W and Cr in an internally consistent way. We conclude that the magmatic histories of these iron meteorite groups are more complex than has been generally assumed.  相似文献   
103.
Alkyl dixanthogens, (ROCSS)2, decompose in aqueous solution in the presence of nucleophiles in many ways.It is proposed here that in alkaline solution the principal methods of decomposition of ethyl dixanthogen are by simultaneous attack of OH? ions on the sulphur-sulphur bond to give products which include xanthate ion (ROCSS?) and peroxide (H2O2) and on the carbon-sulphur bond to give products which include monothiocarbonate ion (ROSCO?), sulphide ion (S2?), and sulphur (S0). Above pH 12 reaction is complete in a few minutes, and more monothiocarbonate than xanthate is formed. At pH 9 the reaction takes over 20 h and more xanthate than monothiocarbonate is formed.The primary products react further to give various ions which depend in part on the pH of the system. In alkaline solution some of the xanthate and peroxide react to give perxanthate (ROCSSO?). In acid solution both xanthate and monothiocarbonate decompose rapidly; CS2 is formed from xanthate and OCS from monothiocarbonate.In the presence of other nucleophiles at pH 9.2, dissolved dixanthogen decomposes much more quickly than with OH? alone, and other reactions occur. With thiosulphate a higher proportion of xanthate is formed together with some xanthyl thiosulphate and monothiocarbonate but no perxanthate. With sulphite (in the absence of oxygen) or cyanide the products include xanthate and monothiocarbonate but no perxanthate. With sulphite in the presence of oxygen, perxanthate is also formed.Suspensions of dixanthogens react slowly but in a similar fashion to dissolved dixanthogens.Longer-chain dixanthogens are much less soluble than ethyl dixanthogen but, in general, react in a similar way. Higher temperatures increase the rate of decomposition by OH?.This work has various implications in operating plants.  相似文献   
104.
The "Little Ice Age": Local and Global Perspectives   总被引:3,自引:0,他引:3  
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105.
Coral reef degradation resulting from nutrient enrichment of coastal waters is of increasing global concern. Although effects of nutrients on coral reef organisms have been demonstrated in the laboratory, there is little direct evidence of nutrient effects on coral reef biota in situ. The ENCORE experiment investigated responses of coral reef organisms and processes to controlled additions of dissolved inorganic nitrogen (N) and/or phosphorus (P) on an offshore reef (One Tree Island) at the southern end of the Great Barrier Reef, Australia. A multi-disciplinary team assessed a variety of factors focusing on nutrient dynamics and biotic responses. A controlled and replicated experiment was conducted over two years using twelve small patch reefs ponded at low tide by a coral rim. Treatments included three control reefs (no nutrient addition) and three + N reefs (NH4Cl added), three + P reefs (KH2PO4 added), and three + N + P reefs. Nutrients were added as pulses at each low tide (ca twice per day) by remotely operated units. There were two phases of nutrient additions. During the initial, low-loading phase of the experiment nutrient pulses (mean dose = 11.5 microM NH4+; 2.3 microM PO4(-3)) rapidly declined, reaching near-background levels (mean = 0.9 microM NH4+; 0.5 microM PO4(-3)) within 2-3 h. A variety of biotic processes, assessed over a year during this initial nutrient loading phase, were not significantly affected, with the exception of coral reproduction, which was affected in all nutrient treatments. In Acropora longicyathus and A. aspera, fewer successfully developed embryos were formed, and in A. longicyathus fertilization rates and lipid levels decreased. In the second, high-loading, phase of ENCORE an increased nutrient dosage (mean dose = 36.2 microM NH4+; 5.1 microM PO4(-3)) declining to means of 11.3 microM NH4+ and 2.4 microM PO4(-3) at the end of low tide) was used for a further year, and a variety of significant biotic responses occurred. Encrusting algae incorporated virtually none of the added nutrients. Organisms containing endosymbiotic zooxanthellae (corals and giant clams) assimilated dissolved nutrients rapidly and were responsive to added nutrients. Coral mortality, not detected during the initial low-loading phase, became evident with increased nutrient dosage, particularly in Pocillopora damicornis. Nitrogen additions stunted coral growth, and phosphorus additions had a variable effect. Coral calcification rate and linear extension increased in the presence of added phosphorus but skeletal density was reduced, making corals more susceptible to breakage. Settlement of all coral larvae was reduced in nitrogen treatments, yet settlement of larvae from brooded species was enhanced in phosphorus treatments. Recruitment of stomatopods, benthic crustaceans living in coral rubble, was reduced in nitrogen and nitrogen plus phosphorus treatments. Grazing rates and reproductive effort of various fish species were not affected by the nutrient treatments. Microbial nitrogen transformations in sediments were responsive to nutrient loading with nitrogen fixation significantly increased in phosphorus treatments and denitrification increased in all treatments to which nitrogen had been added. Rates of bioerosion and grazing showed no significant effects of added nutrients. ENCORE has shown that reef organisms and processes investigated in situ were impacted by elevated nutrients. Impacts were dependent on dose level, whether nitrogen and/or phosphorus were elevated and were often species-specific. The impacts were generally sub-lethal and subtle and the treated reefs at the end of the experiment were visually similar to control reefs. Rapid nutrient uptake indicates that nutrient concentrations alone are not adequate to assess nutrient condition of reefs. Sensitive and quantifiable biological indicators need to be developed for coral reef ecosystems. The potential bioindicators identified in ENCORE should be tested in future research on coral reef/nutrient interactions. Synergistic and cumulative effects of elevated nutrients and other environmental parameters, comparative studies of intact vs. disturbed reefs, offshore vs. inshore reefs, or the ability of a nutrient-stressed reef to respond to natural disturbances require elucidation. An expanded understanding of coral reef responses to anthropogenic impacts is necessary, particularly regarding the subtle, sub-lethal effects detected in the ENCORE studies.  相似文献   
106.
107.
Four high resolution atmospheric general circulation models (GCMs) have been integrated with the standard forcings of the PRUDENCE experiment: IPCC-SRES A2 radiative forcing and Hadley Centre sea surface temperature and sea-ice extent. The response over Europe, calculated as the difference between the 2071–2100 and the 1961–1990 means is compared with the same diagnostic obtained with nine Regional Climate Models (RCM) all driven by the Hadley Centre atmospheric GCM. The seasonal mean response for 2m temperature and precipitation is investigated. For temperature, GCMs and RCMs behave similarly, except that GCMs exhibit a larger spread. However, during summer, the spread of the RCMs—in particular in terms of precipitation—is larger than that of the GCMs. This indicates that the European summer climate is strongly controlled by parameterized physics and/or high-resolution processes. The temperature response is larger than the systematic error. The situation is different for precipitation. The model bias is twice as large as the climate response. The confidence in PRUDENCE results comes from the fact that the models have a similar response to the IPCC-SRES A2 forcing, whereas their systematic errors are more spread. In addition, GCM precipitation response is slightly but significantly different from that of the RCMs.  相似文献   
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