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101.
102.
Luiz Francisco Fontana João Graciano Mendonça Filho 《Marine pollution bulletin》2010,60(10):1674-1681
The aim of this work was to quantify the biopolymers associated to esterase enzymes and identify bacterial respiratory activity in four cores collected in Suruí Mangrove, Guanabara Bay - RJ. Biopolymer concentration was 1000 times lower than previously reported in the literature, indicating the need for creating and establishing eutrophication indicative rates and records compatible with tropical coastal systems. The biochemical representative relationships in the cores were equivalent to those from studies on coastal marine environments made in the Northern Hemisphere. The esterase enzymes in the sediment proved efficient in the mineralization of biopolymers, even with preferentially anaerobic metabolic physiology. Despite the lack of incipient geomicrobiological studies, the results highlighted the possible application of microbiology to a better understanding of geological processes. 相似文献
103.
The main removal mechanisms for the degradations of seven pollutants in wastewater treatment wetlands were analysed, and a mathematical model was established to quantify the removal of each pollutant, based on its main removal mechanisms. Subsurface horizontal flow wetlands were treated as a series of continuous stirred - tank reactors (CSTRs). Kinetic models for the removal of biochemical oxygen demand, chemical oxygen demand, ammonia, total nitrogen and faecal coliforms were established by combining Monod or first - order kinetics with CSTR assumptions. These tentative models account for a wide range of factors that affect wetland performance, but the models have not been proven by ex periment data. Depending on the derivation of various coefficients in the models and verification by actual performance data, this study may provide a starting point for an integrated pollutant removal model to be developed, and experimen tally verified, thereby making a step forward from the current greenbox' approach of wetland design. 相似文献
104.
105.
The adsorption behaviors of Cr(VI) on laterite from Guizhou Province were studied in this paper, and the adsorption mechanism
was discussed as well. Results showed that different mineral compositions in the laterite would cause differences in the capacity
of laterite to absorb Cr(VI). Gibbsite, iron oxide minerals and non-crystalloids are the main contributors to enhancing the
capacity of laterite to absorb Cr(VI). The pH of the solution is an important factor affecting the adsorption of Cr(VI) on
laterite. Acidic environment (pH=2–5) is favorable to the adsorption of Cr(VI). The amount of adsorbed Cr(VI) decreases with
increasing pH of the solution. With increasing initial concentrations of Cr(VI), the amount of adsorbed Cr(VI) increases first,
and then decreases. The optimal adsorption concentration of Cr(VI) on laterite is 250 μg/mL. The adsorption of Cr(VI) on laterite
is a rapid process, about 80% Cr(VI) will be adsorbed within 2 hours. And the adsorption of Cr(VI) on kaolinite is a slow
process. 相似文献
106.
Soil contamination by radioactive Cs from Fukushima Daiichi Nuclear Power Plant accident was investigated. Absorption and desorption experiments of Cs were conducted for several phyllosillicates (kaolinite, sericite, montmorillonite, vermiculite, chrysotile and biotite), zeolite and solid organic matter (dead and green leaves). The results confirmed the characteristic sorption and desorption of Cs by these materials. The 2:1 type phyllosilicate, especially, vermiculite and montmorillonite absorbed Cs well. Heated vermiculite for agricultural use and weathered montmorillonite also adsorbed Cs. Leaves also absorbed Cs considerably but easily desorbed it. In summary, the relative capacity and strength of different materials for sorption of Cs followed the order: zeolite (clinoptilolite) > 2:1 type clay mineral > 1:1 type clay mineral > dead and green leaves. Culture experiments using bacteria of both naturally living on dead leaves in Iitate village, Fukushima Pref. and bacterial strains of Bacillus subtillis, Rhodococus erythropolis, Streptomyces aomiensis and Actinomycetospora chlora were carried out. Non-radioactive 1% Cs solution (CsCl) was added to the culture media. Two types of strong or considerable bacterial uptakes of Cs were found in bacterial cells. One is that Cs was contained mainly as globules inside bacteria and the other is that Cs was absorbed in the whole bacterial cells. The globules consisted mainly of Cs and P. Based on all these results, future diffusion and re-circulation behavior of Cs in the surface environment was discussed. 相似文献
107.
Enhanced coagulation treatment of bacteria‐containing raw water was studied by using three series of composite coagulants, that were prepared by combining polydiallyldimethylammonium chloride (PDADMAC) with different intrinsic viscosity values (0.55–2.47 dL/g) and mass percentages (5–20%) with polyaluminum chloride (PAC), aluminum sulfate (AS), and the composite of aluminum sulfate and ferric chloride (A‐F), respectively. The coagulants were tested by jar tests for the efficiencies to remove bacteria in raw water and to kill bacteria in settled sludge. It was found that when the residual turbidity of supernatant after sedimentation reached the control standard of 2 NTU in drinking water plant, the bacteria‐removing rates of PAC, AS, and A‐F were 92.22, 92.60, and 94.99%, respectively, and the bactericidal rates were 2.52, 1.22, and 2.94%, respectively. Contrastively, the bacteria‐removing rates of PAC/PDADMAC, AS/PDADMAC, and A‐F/PDADMAC could reach 95.45, 96.90, and 98.89%, respectively, and the bactericidal rates could reach 86.60, 91.81, and 96.98%, respectively. It could be deduced from the results that the bactericidal efficiencies of composite coagulants stemmed from the bactericidal action of PDADMAC, and the inorganic coagulants had little bactericidal function. 相似文献
108.
Mounds that have formed around spring vents occur in a variety of environmental settings, many at sites generally difficult or inaccessible for sampling. In contrast, over 500 tufa mounds occur in the dry bed of Searles Lake, California. The mounds range from minor features to 45 m in height; most are 5 to 12 m high. These mounds, composed of calcite and aragonite, formed associated with spring vents in the Pleistocene lake bottom. Thus, analyses of these mounds in Searles Lake provide a model with regard to the origin and architecture of tufa mounds. The mounds consist of four distinctive tufa facies. The initial deposits consist of porous tufa, including the innermost (porous 1) and the outermost (porous 2) deposits, followed by nodular tufa, then columnar tufa, and laminated crusts. There are two simple sequences of tufa deposition. The first sequence is from porous 1 to nodular to laminated crusts and, finally, to porous 2. A second sequence consists of: porous 1 to columnar to laminated crusts and, lastly, to porous 2. Facies changes are a response to changes in environmental conditions from deep water (porous 1 facies) to an essentially dry lake phase (during and after the formation of laminated crusts facies), to deep water (porous 2 facies) and, at the present time, totally dry. The primary constituents that comprise the tufa deposits include thin laminae, pisoids, spherulites, peloids and stromatolite‐like crusts. On the microscopic scale, these constituents dominantly make up nano‐spheres, micro‐rods and rod‐like crystals, as well as other calcified bodies. These constituents are interpreted to be the calcified remains of bacterial bodies. These findings suggest that microbial participation in the construct of other mounds should be a major concern of investigation, both for terrestrial and extraterrestrial spring‐fed mounds. 相似文献
109.
The sphalerite oxidative kinetics under hypergene condition was simulated and studied by means of a mixed flow reactor over a pH range of 1.0 7.8,and at dissolution temperatures from 20 to 55℃,ferric ion concentrations from 1.0×10-5 to 1.0×10-2 mol/L,O 2 flux of 0.5 L/min,and oxidants of ferric ion and O 2.It is indicated that with ferric ion as oxidant,the oxidation rate of sphalerite increases with increasing ferric ion concentration,temperature and decreasing pH value,and under the studied conditions,the dissolution rates of Zn and Cd are approximately identical,with the values of activation energy being 41.75 and 42.51 kJ·mol-1,respectively,suggesting that the oxidation rate of sphalerite is controlled by chemical reactions on mineral surface.However,with O 2 as oxidant,the oxidation mechanism of sphalerite varies with pH value.Oxidation rate decreases with increasing pH value when pH is lower than 5.95,whereas the increase of pH value results in an increase in oxidation rate when pH value is higher than 7.The oxidation rate of sphalerite can be expressed as:R Zn =10 1.1663 [Fe3+] 0 0.154 ·[H+] 0.2659 ·e-41.75/RT or R Cd =10 1.7292 [Fe3+] 0 0.170 ·[H+] 0.2637 ·e-42.51/RT 相似文献
110.
通过对水中含有微量氯苯的吸附特性研究,考察β-环糊精交联聚合物吸附氯苯的动力学、热力学及连续运行条件下的稳定性和再生性能。实验结果表明:β-环糊精交联聚合物吸附氯苯的过程符合准二级动力学模型,即化学吸附是吸附过程的控制步骤;β-环糊精交联聚合物上的等温吸附符合Langmuir吸附等温模型。在15、25、35℃时最大吸附量分别为23.36、28.17、27.85mg/g;动态模拟实验中,当氯苯质量浓度为10mg/L时,氯苯的去除率大于80%。乙醇作为溶剂可以使吸附饱和的β-环糊精交联聚合物再生。 相似文献