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991.
Summary The major objective of the design of safe crowded transmitting antenna sites is not only to determine a safe zone around each individual antenna; rather, to establish safety areas at the antenna site itself, as well as, at the neighboring areas. The requirement is to ascertain the safety regions by considering the following parameters at each Test Point (TP) (or area segment): the contribution of N co-located radiating antennas to the total radiation incident at the TP, the radiation pattern of each antenna, the near/far field region of each antenna, and most importantly, the different Permissible Exposure Limits (PELs) associated with each operating frequency at the antenna site. Implementation of all the above-mentioned aspects in a suitable computer requires resources that only expert knowledgeable organizations possess. The graphically aided tool presented in this paper facilitates the calculation of a “safety zone” for RADHAZ around a crowded antenna site from the knowledge of the “safety ranges” which correspond to the individual transmitting antennas comprising it.  相似文献   
992.
People prone to the effects of river-bank erosion are well aware of the hazard they face, but see it as an unavoidable evil. Communities' lack of success in combating erosion can be attributed to their poverty and to their not knowing about any means to mitigate its effects. Households in safer areas have reduced their dependency on agriculture and developed more scope for non-farm activities, however, this is often difficult given the limited development of local enterprise. The major parameters that influence the adjustment measures after erosion are the education, skills, occupation and financial state of those affected. Those most vulnerable are households very much dependent on agriculture: for them resettlement to distant urban areas is not an option.  相似文献   
993.
994.
995.
A certain number of tagged fish is liberated and assumed to be distributed randomly among a natural fish population. The fish are subjected to a number of fishing experiments within relatively short periods, and lie between equal intervening periods of durationT. Untagged fish are retained, while tagged fish are released during the fishing experiments. Denoting the catchability of untagged fish byq u and that for tagged fish byq t , it is assumed that they are related by the equation “q u =cq t ” wherec is a constant. Denoting the survival rates of tagged fish and the effective fishing effort of commerical fisheries per unit time from the (k-1)th to thek th experiments by t S k andf k , respectively, it is assumed that they vary from period to period. Assuming that during thek th experiment, the number of untagged fish captured and the experimental fishing rate of tagged fish are denoted by u X k and t P k , respectively, then $$\begin{array}{*{20}c} {\frac{{(_u X_k )^2 }}{{[_u X_{(k - 1)} ][_u X_{(k + 1)} ]}} = \frac{{_t S_k }}{{_t S_{(k + 1)} }} \cdot \frac{{e^{ - (1 - c)q_t f_{(k + 1)} T} }}{{e^{ - (1 - c)q_t f_k T} }} \cdot } \\ {\frac{{1 - c_t P_{(k - 1)} }}{{1 - c_t P_k }} \cdot \frac{{(_t P_k )^2 }}{{[_t P_{(k - 1)} ][_t P_{(k + 1)} ]}}.} \\ \end{array}$$ The above equation containsc as a single unknown, while all other terms are supplied by the capture-recapture experiments, exceptf k andf (k+1) which may be obtained from fisheries statistics. A number of the above equations are obtained from several experiments and can be combined into a single equation to obtain an overall estimate forc which can be used to derive estimates for experimental fishing rates, abundance, and instantaneous natural and fishing mortality rates for natural fish populations. These estimates are free from type (A) tagging errors, and have the advantage of taking into consideration the probable different behaviour of tagged and untagged fish.  相似文献   
996.
997.
Evidence is presented that a simple power equation of the formX t X m b(|tt m|)B can describe growth in length and weight of fishes, whereX t denotes fish length or weight at aget, X m is length or weight (L m orW m ) at a reference aget m , andb andB are parameters to be estimated by the least squares. The optimum age of fish populations (t y ) may be estimated by the equationMW m /b=±y B (B/y-M) whereM denotes natural mortality and wherey=t y -t m .  相似文献   
998.
A field study on the removal of Se from agricultural subsurface drainage was conducted from May 1997 to February 2001 in the Tulare Lake Drainage District (TLDD) of San Joaquin Valley, California. A flow-through wetland system was constructed consisting of ten 15- x 76-m unlined cells that were continuously flooded and planted with either a monotype or combination of plants, including sturdy bulrush [Schoenoplectus robustus (Pursh) M.T. Strong], baltic rush (Juncus balticus Willd.), smooth cordgrass (Spartina alterniflora Loisel.), rabbitsfoot grass [Polypogon monspeliensis (L.) Desf.], salt-grass lDistichlis spicata (L.) Greene], cattail (Typha latifolia L.), tule [Schoenoplectus acutus (Muhl. ex Bigelow) A. L?ve & D. L?ve], and widgeon grass (Ruppia maritima L.). One cell had no vegetation planted. The objectives of this research were to evaluate Se removal efficiency of each wetland cell and to carry out a mass balance on Se. The inflow drainage water to the cells had average annual Se concentrations of 19 to 22 microg L(-1) dominated by selenate [Se(VI), 95%]. Average weekly water residence time varied from about 3 to 15 d for Cells 1 through 7 (target 7 d), 19 to 33 d for Cells 8 and 9 (target 21 d), and 13 to 18 d for Cell 10 (target 14 d). Average weekly Se concentration ratios of outflow to inflow ranged from 0.45 to 0.79 and mass ratio (concentration x water volume) from 0.24 to 0.52 for year 2000, that is, 21 to 55% reduction in Se concentration and 48 to 76% Se removal in mass by the wetland, respectively. The nonvegetated cell showed the least Se removal both in concentration and in mass. The global mass balance showed that on the average about 59% of the total inflow Se was retained within the cells and Se outputs were outflow (35%), seepage (4%), and volatilization (2%). Independent measurements of the Se retained in the cells totaled 53% of the total Se inflow: 33% in the surface (0-20 cm) sediment, 18% in the organic detrital layer above the sediment, 2% in the fallen litter, < 1% in the standing plants, and < 1% in the surface water. Thus, about 6% of the total Se inflow was unaccounted for in the internal compartments.  相似文献   
999.
Animal manures contain large amounts of soluble phosphorus (P), which is prone to runoff losses when manure is surface-applied. Here we report the efficacy of alum and three coal combustion by-products in reducing P solubility when added to dairy, swine, or broiler litter manures in a laboratory incubation study. Compared with unamended controls, alum effectively reduced readily soluble P, determined in water extracts of moist manure samples with 1 h of shaking, for all three manures. The reduction ranged from 80 to 99% at treatment rates of 100 to 250 g alum kg(-1) manure dry matter. The fluidized bed combustion fly ash (FBC) reduced readily soluble P by 50 to 60% at a rate of 400 g kg(-1) for all three manures. Flue gas desulfurization by-product (FGD) reduced readily soluble P by nearly 80% when added to swine manure and broiler litter at 150 and 250 g kg(-1). Another by-product, anthracite refuse fly ash (ANT), was ineffective for all three manures. In all cases, reduction in readily soluble P is primarily associated with inorganic phosphorus (P(i)) with little change in organic phosphorus (P(o)). Sequential extraction results indicate that the by-product treatments shifted manure P from H2O-P into a less vulnerable fraction, NaHCO3 - P, while the alum treatment shifted the P into even more stable forms, mostly NaOH-P. Such shifts in P fractions would have little influence on P availability for crops over the long-term but would retard and reduce potential losses of P following manure applications.  相似文献   
1000.
The potential of rhizosphere microbes isolated from common reed [Phragmites australis (Cav.) Trin. ex Steud] plants grown in a subsurface-flow constructed wetland to biomethylate selenate or selenite was studied in liquid cultures under controlled conditions. Total mean percentages of volatilized Se from half-strength Hoagland culture solutions (low C content) supplemented with selenate or selenite and inoculated with cultured rhizosphere microbes after 15 d of incubation were 7.9 and 49.1%, respectively. There was a relative best fit (r = 0.87) between total number of rhizosphere and cultured microbes and the percentage of volatilized Se in Hoagland solution after 15 d of incubation. However, when the same microbes were cultured in tryptic soybean broth (TSB) medium (high C content), the percentages of volatilized Se from selenate and selenite were 1.3 and 1.9%, respectively. The volatilization percentages of Se from selenate or selenite in culture solutions inoculated with rhizosphere suspension instead of cultured rhizosphere microbes were very low (1.2-3.0%) in both cultivation media. In all experiments, selenite was volatilized significantly (p < 0.05) in higher amounts by cultured rhizosphere microbes after 15 d of incubation compared with selenate. Dissolved biomethylated dimethylselenide (DMSe) in water samples taken from the subsurface-flow bed was determined by purging with helium. The DMSe in water samples was indirectly detected up to 2.4 microg Se L(-1), which indicates that part of the produced DMSe was dissolved in the matrix before being released into the atmosphere. Our results show that rhizosphere microbes isolated from common reed plants have a high potential of Se biomethylation and volatilization from selenate and selenite.  相似文献   
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