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161.
An important topic in the registration of pesticides and the interpretation of monitoring data is the estimation of the consequences of a certain concentration of a pesticide for the ecology of aquatic ecosystems. Solving these problems requires predictions of the expected response of the ecosystem to chemical stress. Up until now, a dominant approach to come up with such a prediction is the use of simulation models or safety factors. The disadvantage of the use of safety factors is a crude method that does not provide any insight into the concentration–response relationships at the ecosystem level. On the other hand, simulation models also have serious drawbacks like that they are often very complex, lack transparency, their implementation is expensive and there may be a compilation of errors, due to uncertainties in parameters and processes. In this paper, we present the expert model prediction of the ecological risks of pesticides (PERPEST) that overcomes these problems. It predicts the effects of a given concentration of a pesticide based on the outcome of already performed experiments using experimental ecosystems. This has the great advantage that the outcome is more realistic. The paper especially discusses how this model can be used to translate measured and predicted concentrations of pesticides into ecological risks, by taking data on measured and predicted concentrations of atrazine as an example. It is argued that this model can be of great use to evaluate the outcome of chemical monitoring programmes (e.g. performed in the light of the Water Framework Directive) and can even be used to evaluate the effects of mixtures.  相似文献   
162.
Congenital hypophosphatasia is an autosomal recessive disorder, which usually has a fatal outcome during the neonatal period. This report presents the prenatal diagnosis of hypophosphatasia at 16 weeks of gestation. The characteristic ultrasonic findings in this abnormality demonstrate the superiority of ultrasound as compared with radiography.  相似文献   
163.
A deterministic model for long-term behaviour of contaminants in the rootzone is developed that includes sorption, leaching, and plant uptake. The model is applied to cadmium accumulation in a sandy soil and uptake of cadmium by barley. Sensitivity analysis showed that the sensitivity of the leaching rate to changes in soil chemical and soil physical parameters decreases as a function of time, and becomes zero when steady state is reached. In contrast, accumulation of cadmium in soil and the plant uptake rate of barley are increasingly sensitive to soil chemical and soil physical parameters as time preceeds. To analyse cadmium behaviour in a field that is heterogeneous with respect to soil physical properties, the interstitial flow velocity was assumed to be a random, lognormally distributed variate. Using Monte Carlo simulation, the average plant uptake rate appeared to be much higher in the stochastic analysis than in the deterministic approach. Steady state is reached after a very long period of time. For a lognormally distributed proton activity, causing heterogeneity with respect to the sorption capacity of the soil, the model predicted similar deviations from the deterministic approach. It is concluded that reference values for groundwater and crop quality are exceeded earlier in a heterogeneous field than in a homogenous soil profile. Moreover, when average values suggest an acceptable situation, variability of the leaching rate and the plant uptake rate can still cause exceedance of reference values in part of the field. Therefore, it is reasoned that environmental quality standards should take soil heterogeneity into account.  相似文献   
164.
165.
The Aerosol Research and Inhalation Epidemiology Study (ARIES) was designed to provide high-quality measurements of PM2.5, its components, and co-varying pollutants for an air pollution epidemiology study in Atlanta, GA. Air pollution epidemiology studies have typically relied on available data on particle mass often collected using filter-based methods. Filter-based PM2.5 sampling is susceptible to both positive and negative errors in the measurement of aerosol mass and particle-phase component concentrations in the undisturbed atmosphere. These biases are introduced by collection of gas-phase aerosol components on the filter media or by volatilization of particle phase components from collected particles. As part of the ARIES, we collected daily 24-hr PM2.5 mass and speciation samples and continuous PM2.5 data at a mixed residential-light industrial site in Atlanta. These data facilitate analysis of the effects of a wide variety of factors on sampler performance. We assess the relative importance of PM2.5 components and consider associations and potential mechanistic linkages of PM2.5 mass concentrations with several PM2.5 components. For the 12 months of validated data collected to date (August 1, 1998-July 31, 1999), the monthly average Federal Reference Method (FRM) PM2.5 mass always exceeded the proposed annual average standard (12-month average = 20.3 +/- 9.5 micrograms/m3). The particulate SO4(2-) fraction (as (NH4)2SO4) was largest in the summer and exceeded 50% of the FRM mass. The contribution of (NH4)2SO4 to FRM PM2.5 mass dropped to less than 30% in winter. Particulate NO3- collected on a denuded nylon filter averaged 1.1 +/- 0.9 micrograms/m3. Particle-phase organic compounds (as organic carbon x 1.4) measured on a denuded quartz filter sampler averaged 6.4 +/- 3.1 micrograms/m3 (32% of FRM PM2.5 mass) with less seasonal variability than SO4(2-).  相似文献   
166.
Chemo-denitrification of nitrate-polluted water   总被引:1,自引:0,他引:1  
Nitrate-nitrogen reduction was studied in the presence of ferrous iron and a copper catalyst. In a batch system, it was found that the reduction was very fast at pH 8.1 and slow at pH 7.5. A temporary accumulation of nitrate and hydroxylamine was noted. It was found that the reduction of nitrite-nitrogen in the presence of ferrous iron partly continued to ammonium. Decreasing the amount of reagents led to a slower reduction rate but a lower accumulation of nitrite and hydroxylamine. A continuous system was described whereby more than 50% of the initial nitrate could be removed.  相似文献   
167.
The adsorption data of the pesticides have been correlated with several molecular parameters. The most significant relation was obtained with a multilinear combination of the hydrophobicity constant π and the Hildebrand's constant δ which is influenced by the molecular interactions properties of the aromatic ring of the solutes.  相似文献   
168.
Laboratory and modeling studies were conducted to assess the potential performance of a permeable reactive barrier constructed of a natural zeolite material at the West Valley Demonstration Project in western New York State. The results of laboratory column tests indicated that the barrier material would be effective at removing strontium from groundwater under natural gradient conditions. Two one-dimensional contaminant transport models were developed to interpret the data. A single-solute retardation factor model provided good agreement with the column test data, but time-consuming extraction and analysis of the zeolite material was required to parameterize the model. A preliminary six-solute model was also developed based on the assumption of competitive cation exchange as the primary removal mechanism. Both models yielded similar predictions of the long-term performance of the barrier, but the cation exchange model predicted higher effluent concentrations during the first 1000 pore volumes of operation. The cation exchange framework has several advantages, including the ability to calibrate the model using only data from column effluent samples, and the ability to account for site-specific differences in the groundwater cation composition. However, additional laboratory work is needed to develop a suitably robust model.  相似文献   
169.
Thermophilic-anaerobic digestion in a single-stage, mixed, continuous-flow reactor is not approved in the United States as a process capable of producing Class A biosolids for land application. This study was designed to evaluate the inactivation of pathogens and indicator organisms in such a reactor followed by batch treatment in a smaller reactor. The combined process was evaluated at 53 degrees C with sludges from three different sources and at 51 and 55 degrees C with sludge from one of the sources. Feed sludge to the continuous-flow reactor was spiked with the pathogen surrogates Ascaris suum and vaccine-strain poliovirus. Feed and effluent were analyzed for these organisms and for indigenous Salmonella spp., fecal coliforms, Clostridium perfringens spores, and somatic and male-specific coliphages. No viable Ascaris eggs were observed in the effluent from the continuous reactor at 53 or 55 degrees C, with greater than 2-log removals across the digester in all cases. Approximately 2-log removal was observed at 51 degrees C, but all samples of effluent biosolids contained at least one viable Ascaris egg at 51 degrees C. No viable poliovirus was found in the digester effluent at any of the operating conditions, and viable Salmonella spp. were measured in the digester effluent in only one sample throughout the study. The ability of the continuous reactor to remove fecal coliforms to below the Class A monitoring limit depended on the concentration in the feed sludge. There was no significant removal of Clostridium perfringens across the continuous reactor under any condition, and there also was limited removal of somatic coliphages. The removal of male-specific coliphages across the continuous reactor appeared to be related to temperature. Overall, at least one of the Class A pathogen criteria or the fecal coliform limit was exceeded in at least one sample in the continuous-reactor effluent at each temperature. Over the range of temperatures evaluated, the maximum time required to meet the Class A criteria by batch treatment of the continuous-reactor effluent was 1 hour for Ascaris suum and Salmonella spp. and 2 hours for fecal coliforms.  相似文献   
170.
Gaseous elemental and total (elemental + oxidized) mercury (Hg) in the flue gas from a coal-fired boiler was measured by a modified ultraviolet (UV) spectrometer. Challenges to Hg measurement were the spectral interferences from other flue gas components and that UV measures only elemental Hg. To eliminate interference from flue gas components, a cartridge filled with gold-coated sand removed elemental Hg from a flue gas sample. The Hg-free flue gas was the reference gas, eliminating the spectral interferences. To measure total Hg by UV, oxidized Hg underwent a gas-phase, thermal-reduction in a quartz cell heated to 750 degrees C. Simultaneously, hydrogen was added to flash react with the oxygen present forming water vapor and preventing Hg re-oxidation as it exits the cell. Hg concentration results are in parts per billion by volume Hg at the flue gas oxygen concentration. The modified Hg analyzer and the Ontario Hydro method concurrently measured Hg at a field test site. Measurements were made at a 700-MW steam turbine plant with scrubber units and selective catalytic reduction. The flue gas sampled downstream of the selective catalytic reduction contained 2100 ppm SO2 and 75 ppm NOx. Total Hg measured by the Hg analyzer was within 20% of the Ontario Hydro results.  相似文献   
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