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21.
This paper describes simulation experiments in which glucose and cellulose were reacted with polysulphide and hydrogen sulphide at ambient temperatures in an aqueous environment. Organic sulphur containing compounds were formed that yield several thiophenes upon pyrolysis/evaporation. The experiments show that interaction of carbohydrates with hydrogen sulphide or polysulphides is a possible way for carbohydrates to react in very recent sediments. From the results of this study it can be concluded that carbohydrate carbon can be preserved in sediments in a form that is resistant to microbial attack and that will have a greater potential for survival during diagenesis than the carbohydrate precursor. 相似文献
22.
A series of novel long-chain 3,4-dialkylthiophenes (C36–C54) was identified in a number of sediments ranging from Pleistocene to Cretaceous. The identifications were based on mass spectral characterisation, desulphurisation and mass spectral data of synthesised model compounds. These organic sulphur compounds are probably formed by sulphur incorporation into mid-chain dimethylalkadienes with two methylenic double bonds. These putative precursor lipids are unprecedented and may be considered rather unusual. The distribution of 3,4-dialkylthiophenes in sediments varies considerably with the depositional palaeoenvironment, indicating that these compounds have a potential as molecular markers reflecting changes in palaeoenvironment. 相似文献
23.
A statistically relevant correlation between the reaction rate coefficient, k
OH, for the OH radical reaction with 161 organic compounds in the gas phase at 300 K, and the corresponding vertical ionisation energies E
i,v, reveals two classes of compounds: aromatics where –log(k
OH/cm3s-1)3/2E
i,v(eV)–2 and aliphatics where –log(k
OH/cm3s-1)4/5E
i,v(eV)+3. The prediction of the rate coefficient, k
OH, for the reaction of OH with organic molecules from the above equations has a probability of about 90%. Assuming a global diurnal mean of the OH radical concentration of 5×105 cm3, the upper limit of the tropospheric half-life of organic compounds and their persistence can be estimated. 相似文献
24.
Air was injected through a well in a thin transparent tank filled with saturated glass beads to study how the size and air
saturation of air sparging plumes are affected by particle size and gradation; operational parameters such as injection pressure,
well depth, injection pressure pulsing; and well outlet configuration. V-shaped air plumes with an apex between 40° and 60°
were obtained for all tests. The air pressure required to initiate sparging agreed closely with the sum of the air entry pressure
and the hydrostatic pressure, with higher initiation pressures required in the fine and well-graded beads. Higher air flow
rates and air saturations were obtained in coarser beads at a given pressure, and the variation in flow rate was consistent
with estimated air permeabilities. Peak average air saturations were 28–56% for the coarse-medium beads, 10% for the well-graded
beads, and 8% for the fine beads. Air saturation and the radius of influence increased modestly (<40%) as the normalized injection
pressure exceeded 0.1. Radius of influence increased by approximately a factor of two as the well depth increased, but leveled
off once the ratio of radius of influence to well depth reached 0.60–1.05. Pulsing of injection pressure had no effect on
the initiation pressure, air flow rate, or air saturation, but increased the size of the air plume and the radius of influence
slightly (<15%). Well outlet configuration had only a slight affect the radius of influence (<10%), air saturation (<10%),
or air flow rate (<12%). Dye testing showed that water surrounding the air plume circulated during continuous and pulsed sparging.
However, pulsed sparging resulted in greater and more defined circulation of water within and adjacent to the air plume, which
should reduce mass transfer limitations during sparging. 相似文献
25.
水资源中氯代烃污染物的去除方法 总被引:3,自引:0,他引:3
随着工业化的发展。氯代有机溶剂使用越来越广泛。并且难于去除。在20世纪90年代初期,人们就已认识到用Fe^0恢复污染的地下水的潜力。国外正在研究帮使用扔几种还原挥发性氯代烃的还原反应介质,尤其要提高的是双金属反应系统,反应速度快,而且脱Cl中国难解产物少,目前国也只停留在实验室研究阶段,个别做了地上反应器的验证实验,它的脱Cl机理、介质钝化和完全脱Cl问题还有待于进一步研究。 相似文献
26.
Victor B. MAGLAMBAYAN Daizo ISHIYAMA Toshio MIZUTA Osamu MATSUBAYA Yohei ISHIKAWA 《Resource Geology》2001,51(2):107-116
Abstract: The disseminated Au‐Ag telluride Bulawan deposit, Negros island, Philippines, is hosted by dacite porphyry breccia pipes which formed in a Middle Miocene dacite porphyry stock. Electrum and Au‐Ag tellurides occur mostly as grains intergrown with or filling voids between sphalerite, pyrite, chalcopyrite, galena and tennantite. Calcite, quartz and rare dolomite are the principal gangue minerals. Four types of alteration were recognized in the deposit, namely; propylitic, K‐feldspar‐sericitic, sericitic and carbonate alteration. Carbonate alteration is correlatable to the gold deposition stage and occurs mostly along fault zones. The δ18O and δ13C compositions of calcite and dolomite in propylite zone and ore‐stage dacite porphyry breccia were determined. The δ18O values of calcite in propylitized andesite range from +12.2 to +14.7%, and their δ13C values range from ‐6.1 to ‐1.0%. The δ18O values of calcite and dolomite in sericite‐ and carbonate‐altered, mineralized dacite porphyry breccia and dacite porphyry rocks range from +15.1 to +23.1%, and the δ13C values of calcite and dolomite range from ‐3.9 to +0.9%. The δ18O and δ13C values of the hydrothermal fluids were estimated from inferred temperatures of formation on the basis of fluid inclusion microthermometry. The δ18O values of hydrothermal fluid for the propylitic alteration were calculated to be +8.5 ‐ +9.5%, assuming 375°C. On the other hand, the δ18O values of ore solutions for base metal and Au mineralization were computed to be +13.6 ‐ +14.6%, assuming 270°C. The hydrothermal fluids that formed the Bulawan deposit are dilute and 18O‐enriched fluids which reacted with 18O‐ and 13C‐rich wallrocks such as limestone. 相似文献
27.
28.
A total of 11 earthquakes with 15 Rayleigh wave paths, recorded at 11 broadband digital PASSCAL seismometers installed in
the Tibet Plateau by the Sino-U.S. joint research group, were used to determine the phase velocity and attenuation coefficient
of surface waves in periods of 10–130 s. The average shear wave velocity and quality factor {ie271-1} structures in the crust
and upper mantle were obtained in this region. The result shows the average {ie271-2} is low and there exists a high attenuation
({ie271-3}=93–141) layer in the crust. The depth range of the low {ie271-4} value layer (16–42 km) is consistent with the
range of low velocity layer (21–51 km) in the crust. Below 63 km in the lower crust, {ie271-5} decreases with depth from 114
to 34 at depth of 180 km. The low shear wave velocity and low value of {ie271-6} at the same depth range in the crust indicate
that the rocks in the range is probably melted or partially melted. According to the shear wave velocity structure, the average
thickness of the crust is about 71 km and a clear velocity discontiniuty appears at the depth of 51 km. The low-velocity zone
(4. 26 km/s) at depth of 96–180 km may be corresponding to the asthenosphere.
Contribution No. 96A0047, Institute of Geophysics, SSB, China.
This study was supported by the National Natural Science Foundation of China. 相似文献
29.
R. N. Colvile T. W. Choularton J. N. Cape B. J. Bandy K. N. Bower R. A. Burgess T. J. Davies G. J. Dollard M. W. Gallagher K. J. Hargreaves B. M. R. Jones S. A. Penkett R. L. Storeton-West 《Journal of Atmospheric Chemistry》1996,24(3):211-239
Four case studies are described, from a three-site field experiment in October/November 1991 using the Great Dun Fell flow-through reactor hill cap cloud in rural Northern England. Measurements of total odd-nitrogen nitrogen oxides (NO
y
) made on either side of the hill, before and after the air flowed through the cloud, showed that 10 to 50% of the NO
y
, called NO
z
, was neither NO nor NO2. This NO
z
failed to exhibit a diurnal variation and was often higher after passage through cloud than before. No evidence of conversion of NO
z
to NO3
- in cloud was found. A simple box model of gas-phase chemistry in air before it reached the cloud, including scavenging of NO3 and N2O5 by aerosol of surface area proportional to the NO2 mixing ratio, shows that NO3 and N2O5 may build up in the boundary layer by night only if stable stratification insulates the air from emissions of NO. This may explain the lack of evidence for N2O5 forming NO3
- in cloud under well-mixed conditions in 1991, in contrast with observations under stably stratified conditions during previous experiments when evidence of N2O5 was found. Inside the cloud, some variations in the calculated total atmospheric loading of HNO2 and the cloud liquid water content were related to each other. Also, indications of conversion of NO
x
to NO
z
were found. To explain these observations, scavenging of NO
x
and HNO2 by cloud droplets and/or aqueous-phase oxidation of NO2
- by nitrate radicals are considered. When cloud acidity was being produced by aqueous-phase oxidation of NO
x
or SO2, NO3
- which had entered the cloud as aerosol particles was liberated as HNO3 vapour. When no aqueous-phase production of acidity was occurring, the reverse, conversion of scavenged HNO3 to particulate NO3
-, was observed. 相似文献
30.
Oliver Wild Oliver V. Rattigan Roderic L. Jones John A. Pyle R. Anthony Cox 《Journal of Atmospheric Chemistry》1996,25(2):167-199
The Cambridge 2-D Eulerian model has been used to study the potential atmospheric distributions and lifetimes of a number of CFC replacement compounds and their degradation products. The study has focused on HFC 134a and HCFCs 123, 141b and 142b and the major products formed by their atmospheric degradation. The loss of these compounds and their products by hydroxyl radical attack, photolysis and in-cloud hydrolysis have been investigated. The study has shown that HCFCs 141b and 142b have sufficiently long lifetimes to enter the stratosphere in significant quantities, where degradation leads to an increase in the total stratospheric chlorine concentration. The study has also highlighted areas where further experimental work would be valuable, in particular characterisation of the product channels for the degradation reactions and determination of the removal rates of the products in the aqueous phase. 相似文献