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991.
M. Palos Ladeiro A. Bigot D. Aubert J. Hohweyer L. Favennec I. Villena A. Geffard 《Environmental science and pollution research international》2013,20(2):778-789
Toxoplasma gondii, Cryptosporidium parvum, and Giardia duodenalis are human waterborne protozoa. These worldwide parasites had been detected in various watercourses as recreational, surface, drinking, river, and seawater. As of today, water protozoa detection was based on large water filtration and on sample concentration. Another tool like aquatic invertebrate parasitism could be used for sanitary and environmental biomonitoring. In fact, organisms like filter feeders could already filtrate and concentrate protozoa directly in their tissues in proportion to ambient concentration. So molluscan shellfish can be used as a bioindicator of protozoa contamination level in a site since they were sedentary. Nevertheless, only a few researches had focused on nonspecific parasitism like protozoa infection on aquatic invertebrates. Objectives of this review are twofold: Firstly, an overview of protozoa in worldwide water was presented. Secondly, current knowledge of protozoa parasitism on aquatic invertebrates was detailed and the lack of data of their biological impact was pointed out. 相似文献
992.
A. Durán J.M. Monteagudo I. San Martín M. Aguirre 《Journal of environmental management》2010,91(9):1840-1846
The aim of this work was to study the mineralization of wastewater effluent from an integrated-gasification combined-cycle (IGCC) power station sited in Spain to meet the requirements of future environmental legislation. This study was done in a pilot plant using a homogeneous photo-Fenton oxidation process with continuous addition of H2O2 and air to the system.The mineralization process was found to follow pseudo-first-order kinetics. Experimental kinetic constants were fitted using neural networks (NNs). The NNs model reproduced the experimental data to within a 90% confidence level and allowed the simulation of the process for any values of the parameters within the experimental range studied. At the optimum conditions (H2O2 flow rate = 120 mL/h, [Fe(II)] = 7.6 mg/L, pH = 3.75 and air flow rate = 1 m3/h), a 90% mineralization was achieved in 150 min.Determination of the hydrogen peroxide consumed and remaining in the water revealed that 1.2 mol of H2O2 was consumed per each mol of total organic carbon removed from solution. This result confirmed that an excess of dissolved H2O2 was needed to achieve high mineralization rates, so continuous addition of peroxide is recommended for industrial application of this process.Air flow slightly improved the mineralization rate due to the formation of peroxo-organic radicals which enhanced the oxidation process. 相似文献
993.
Jürgen Warrelmann Hartmut Kochler Tobias Frische Ingo Dobner Ulrich Walter Wolfgang Heyser 《Environmental Sciences Europe》2000,12(6):351-357
On the area of a former ordnance plant (‘Werk Tanne’, Clausthal-Zellerfeld, Germany), a field experiment for phytoremediation of TNT-contaminated soils has been carried out since May 1999. The concept is based on a stepwise degradation of TNT by white-rot fungi and mycorrhiza within the rhizosphere of site-specific seedlings. An appropiate site with contaminants in the surface-soil was prepared with a large-scale soil grader and subsequently divided into different experimental plots, including an uncontaminated control as well as a contaminated plot without treatment. Planting of the selected trees and shrubs (infected with mycorrhiza during nursery) and inoculation with wood chips (inoculated with white-rot fungi) is followed by a detailed monitoring of the experimental plots (chemical analyses, biotest-battery, ecological field indicators). For the evaluation of the results, multivariate methods are applied. 相似文献
994.
995.
996.
Heinz Rüdel Winfried Schröder Karl Theo von der Trenck Gerhard Andreas Wiesmüller 《Environmental science and pollution research international》2009,16(5):486-498
Background Due to the requirements of the EU Water Framework Directive and other legal regulations (e.g., national laws like the German
Federal Soil Protection Act), but also due to the implementation of the new EU chemicals management system REACH, environmental
monitoring will gain increasing importance for the surveillance of environmental quality as well as for the assessment of
chemicals. Against this background, the Work Group on ‘Environmental Monitoring’ of the Division of ‘Environmental Chemistry
and Ecotoxicology’ within the German Chemical Society has compiled a position paper on substance-related environmental monitoring.
Scope Core elements of this position paper are the definitions of important terms like monitoring, exposure monitoring, effect monitoring,
and integrated monitoring. Moreover, temporal and spatial aspects (monitoring of spatial distributions, trend monitoring,
and retrospective monitoring) and their applications are discussed. The main focus of this position paper is the coverage
of aspects which have to be observed for the preparation and implementation of a monitoring program. Essential is the clear
specification of the targets of the monitoring which determine the development of the monitoring concept and its realization,
e.g., if environmental media (compartments) or organisms are most appropriate as samples for the aim of the study. Of course,
also the properties of the target substances are important (e.g., lipophilicity/bioaccumulation as pre-requisite for an exposure
monitoring with organisms). Finally, the monitoring phases of sample planning, sampling, storage and transport of samples,
selection of analytical methods, quality assurance measures as well as reporting are discussed.
Perspectives An important issue for the future is to link the quantification of chemicals in environmental compartments (exposure and pollution
monitoring) more closely to the study of biological effects (effect monitoring) than has been the case up to now. Furthermore,
by inclusion of a spatial differentiation, a comprehensive evaluation of the state of an ecosystem can be obtained and the
relevance of the results improved. Practical examples of monitoring studies which illustrate various aspects covered in this
position paper will be presented in a series of publications by members of the Work Group in the following issues of this
journal.
相似文献
Gerhard Andreas WiesmüllerEmail: |
997.
Benzyl-penicillin (Penicillin G) transformation in aqueous solution at low temperature under controlled laboratory conditions 总被引:1,自引:0,他引:1
Antibiotics are released into the environment in a variety of ways: via wastewater effluent as a result of incomplete metabolism in the body after use in human therapy, as runoff after use in agriculture, through improper disposal by private households or hospitals or through insufficient removal by water treatment plants. Unlike in most European countries, in Arctic regions effluents are not suitably treated prior to their release into the aquatic environment. Also, many of the scattered human settlements in remote regions of the Arctic do not possess sewage treatment facilities and pharmaceutical residues therefore enter the aqueous environment untreated. Only limited data are available on the biodegradation of antibiotics under Arctic conditions. However, such information is needed to estimate the potential harm of antibiotics for the environment. Pen-G is used in this study since it is a widely prescribed antibiotic compound whose environmental properties have not yet been investigated in detail. Thus, for a very first assessment, the OECD approved biodegradation Zahn-Wellens test (ZWT, OECD 302 B) was used to study biodegradation and non-biotic elimination of the antibiotic Benzyl-penicillin (Pen-G) at different temperatures (5°C, 12.5°C and 20°C). The testing period was extended from the OECD standard of 28-42d. In addition to dissolved organic carbon (DOC), Pen-G levels and major transformation products were recorded continuously by LC-ion-trap-MS/MS. DOC monitoring revealed considerable temperature dependence for the degradation process of Pen-G. DOC loss was slowest at 5°C and considerably faster at 12.5°C and 20°C. In the initial step of degradation it was found that Pen-G was hydrolyzed. This hydrolyzed Pen-G was subsequently further degraded by decarboxylation, the result of which was 2-(5,5-dimethyl-1,3-thiazolidin-2-yl)-2-(2-phenylacetamido)acetic acid. Furthermore, direct elimination of 2-phenyl-acetaldehyde from the hydrolyzed and decarboxylated Pen-G also led to the formation of 2-[amino(carboxy)methyl]-5,5-dimethyl-1,3-thiazolidone-4-carboxylic acid. Since biodegradation slows down considerably at a low temperature, the resulting transformation products had considerably longer residence times at 5°C compared to higher temperature conditions within the 42-d experiment. The results presented here clearly demonstrate that a risk assessment for pharmaceuticals present in low ambient temperature environments (i.e. the Arctic) cannot be based on test results obtained under standard laboratory conditions (i.e. 20°C ambient temperatures). 相似文献
998.
D. Martin C.S. Price I.R. White G. Nickless K.F. Petersson R.E. Britter A.G. Robins S.E. Belcher J.F. Barlow M. Neophytou S.J. Arnold A.S. Tomlin R.J. Smalley D.E. Shallcross 《Atmospheric environment (Oxford, England : 1994)》2010,44(25):3043-3052
As part of the DAPPLE programme two large scale urban tracer experiments using multiple simultaneous releases of cyclic perfluoroalkanes from fixed location point sources was performed. The receptor concentrations along with relevant meteorological parameters measured are compared with a three screening dispersion models in order to best predict the decay of pollution sources with respect to distance. It is shown here that the simple dispersion models tested here can provide a reasonable upper bound estimate of the maximum concentrations measured with an empirical model derived from field observations and wind tunnel studies providing the best estimate. An indoor receptor was also used to assess indoor concentrations and their pertinence to commonly used evacuation procedures. 相似文献
999.
X. Q. Liang Z. Y. Nie M. M. He R. Guo C. Y. Zhu Y. X. Chen Küppers Stephan 《Environmental science and pollution research international》2013,20(10):6972-6979
One strategy to combat nitrate (NO3-N) contamination in rivers is to understand its sources. NO3-N sources in the East Tiaoxi River of the Yangtze Delta Region were investigated by applying a 15N–18O dual isotope approach. Water samples were collected from the main channel and from the tributaries. Results show that high total N and NO3-N are present in both the main channel and the major tributaries, and NO3-N was one of the most important N forms in water. Analysis of isotopic compositions (δ 18O, δD) of water suggests that the river water mainly originated from three tributaries during the sampling period. There was a wide range of δ 15N-NO3 (?1.4 to 12.4 ‰) and a narrow range of δ 18O-NO3 (3.7 to 9.0 ‰) in the main channel waters. The δ 15N and δ 18O-NO3 values in the upper, middle, and lower channels along the river were shifted as 8.2, 3.5, and 9.5 ‰, and 9.0, 4.2, and 6.0 ‰, respectively. In the tributary South Tiao, the δ 15N and δ 18O-NO3 values were as high as 9.5 and 7.0 ‰, while in the tributaries Mid Tiao and North Tiao, NO3-N in most of the samples had relatively low δ 15N and δ 18O-NO3 values from 2.3 to 7.5 ‰ and 4.7 to 7.0 ‰, separately. Our results also suggest that the dual isotope approach can help us develop the best management practice for relieving NO3-N pollution in the rivers at the tributary scale. 相似文献
1000.
A. Camacho R. Devesa I. Serrano S. Blázquez L. Matia 《Journal of environmental radioactivity》2010,101(12):1048-1054
A study is presented on the distribution of 234U, 238U, 235U isotopes in surface water of the Llobregat river basin (Northeast Spain), from 2001 to 2006. Sixty-six superficial water samples were collected at 16 points distributed throughout the Llobregat river basin. Uranium isotopes were measured by alpha spectrometry (PIPS detectors). The test procedure was validated according to the quality requirements of the ISO17025 standard. The activity concentration for the total dissolved uranium ranges from 20 to 261 mBq L−1. The highest concentrations of uranium were detected in an area with formations of sedimentary rock, limestone and lignite. A high degree of radioactive disequilibrium was noted among the uranium isotopes. The 234U/238U activity ratio varied between 1.1 and 1.9 and the waters with the lowest uranium activity registered the highest level of 234U/238U activity ratio. Correlations between uranium activity in the tested water and chemical and physical characteristics of the aquifer were found. 相似文献