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71.
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Iodine-129:iodine-127 ratios were determined using accelerator mass spectrometry in 34 Arctic marine algae collected between 1930 and 1993. A smaller set (5) of marine algae were also analyzed mass spectrometrically to determine plutonium-isotope ratios. The 129I:127I ratio increased as much as three orders of magnitude from a mean of <1×10−11 (atom/atom) in the pre-nuclear era (before 1945) to nearly 1000×10−11 in 1993 for marine algae collected from the Novaya Zemlya archipelago separating the Barents and Kara Seas. The predominant basis for the higher ratios in the Novaya Zemlya kelps appears to be upcurrent sources of 129I from nuclear fuel-reprocessing facilities at Sellafield (UK) and La Hague (France). Relatively high 241Pu:239Pu ratios (compared to observed bomb fallout at boreal latitudes, decay corrected to the date of collection) also corroborate the influence of non-fallout sources. The small size of the data set precludes determining if there are significant contributions of 129I and other radionuclides from Russian sources. In contrast, marine algae collected between 1969 and 1993 in the Bering, Beaufort and East Siberian Seas had much lower 129I:127I ratios (mean=14.04×10−11±3.15 SD) than those observed in the European Arctic. The narrow range of ratios in Ameriasian Arctic kelps, and the modest change over that time period, indicate that there were no major contributions of non-fallout 129I to North American Arctic surface waters at the time that the algae were collected. The potential for timing the transport of fuel-reprocessed 129I through analysis of additional archived samples is outlined. Received: 10 November 1997 / Accepted: 24 February 1998  相似文献   
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Nalli S  Cooper DG  Nicell JA 《Chemosphere》2006,65(9):1510-1517
The commonly used plasticizers di-ethylhexyl phthalate (DEHP) and di-ethylhexyl adipate (DEHA) are known to partially degrade in the presence of soil microorganisms, such as Rhodococcus rhodochrous, releasing persistent and toxic metabolites. The metabolites adipic acid and 2-ethylhexanol were both shown to inhibit growth of the degrading microbe. 2-Ethylhexanol enhanced the activity of ethanol dehydrogenase - an enzyme involved in its metabolism - but the activity of this enzyme was inhibited by adipic acid. The metabolite usually seen in the highest concentrations - 2-ethylhexanoic acid - did not exhibit any evidence of inhibition. It was shown that the high concentration of this metabolite was due to the inability of R. rhodochrous to degrade it. Comparisons with other small carboxylic acids supported the argument that the ethyl branch was the reason for the resistance of 2-ethylhexanoic acid to degradation. The hydrophobicity of the cell surface was shown to be a factor in plasticizer degradation. The primary carbon source could be either water-soluble or hydrophobic and a hydrophobic substrate led to a cell surface that attracted the plasticizer and facilitated degradation. The most hydrophobic of the plasticizers, DEHP, was particularly sensitive to this effect.  相似文献   
76.
The relative accuracy (RA) of a newly developed mercury continuous emissions monitor, based on X-ray fluorescence, was determined by comparing analysis results at coal-fired plants with two certified reference methods (American Society for Testing and Materials [ASTM] Method D6784-02 and U.S. Environment Protection Agency [EPA] Method 29). During the first determination, the monitor had an RA of 25% compared with ASTM Method D6784-02 (Ontario Hydro Method). However, the Ontario Hydro Method performed poorly, because the mercury concentrations were near the detection limit of the reference method. The mercury in this exhaust stream was primarily elemental. The second test was performed at a U.S. Army boiler against EPA Reference Method 29. Mercury and arsenic were spiked because of expected low mercury concentrations. The monitor had an RA of 16% for arsenic and 17% for mercury, meeting RA requirements of EPA Performance Specification 12a. The results suggest that the sampling stream contained significant percentages of both elemental and oxidized mercury. The monitor was successful at measuring total mercury in particulate and vapor forms.  相似文献   
77.
The first nuclear explosion test, named the Trinity test, was conducted on July 16, 1945 near Alamogordo, New Mexico. In the tremendous heat of the explosion, the radioactive debris fused with the local soil into a glassy material named Trinitite. Selected Trinitite samples from ground zero (GZ) of the test site were investigated in detail for radioactivity. The techniques used included alpha spectrometry, high-efficiency gamma-ray spectrometry, and low-background beta counting, following the radiochemistry for selected radionuclides. Specific activities were determined for fission products (90Sr, 137Cs), activation products (60Co, 133Ba, 152Eu, 154Eu, 238Pu, 241Pu), and the remnants of the nuclear fuel (239Pu, 240Pu). Additionally, specific activities of three natural radionuclides (40K, 232Th, 238U) and their progeny were measured. The determined specific activities of radionuclides and their relationships are interpreted in the context of the fission process, chemical behavior of the elements, as well as the nuclear explosion phenomenology.  相似文献   
78.
Wildlife resource selection studies typically compare used to available resources; selection or avoidance occurs when use is disproportionately greater or less than availability. Comparing used to available resources is problematic because results are often greatly influenced by what is considered available to the animal. Moreover, placing relocation points within resource units is often difficult due to radiotelemetry and mapping errors. Given these problems, we suggest that an animal’s resource use be summarized at the scale of the home range (i.e., the spatial distribution of all point locations of an animal) rather than by individual points that are considered used or available. To account for differences in use-intensity throughout an animal’s home range, we model resource selection using kernel density estimates and polytomous logistic regression. We present a case study of elk (Cervus elaphus) resource selection in South Dakota to illustrate the procedure. There are several advantages of our proposed approach. First, resource availability goes undefined by the investigator, which is a difficult and often arbitrary decision. Instead, the technique compares the intensity of animal use throughout the home range. This technique also avoids problems with classifying locations rigidly as used or unused. Second, location coordinates do not need to be placed within mapped resource units, which is problematic given mapping and telemetry error. Finally, resource use is considered at an appropriate scale for management because most wildlife resource decisions are made at the level of the patch. Despite the advantages of this use-intensity procedure, future research should address spatial autocorrelation and develop spatial models for ordered categorical variables.  相似文献   
79.
A toxicological evaluation was conducted on wetland habitats created as a result of run-off from agricultural areas. These temporary wetlands were created by using drop pipes as a means of reducing erosional cutting in agricultural fields. Toxicity bioassays utilizing bacterial bioluminescence and Hyalella azteca were used to assess sediment pore water and whole sediment, respectively. Inhibition of bacterial bioluminescence was initially used to determine relative toxicities of pore water from ten wetland sites. Constructed wetland sites were compared to the University of Mississippi Biological Field Station, a relatively pristine reference site. The H. azteca ten day sediment toxicity test was utilized to assess sediment from four selected sites using survival and growth as toxicological endpoints. Results from the toxicological evaluation, along with extensive ecological evaluations, were used to assess the best approach for implementation of temporary wetland habitats with existing agricultural practices.  相似文献   
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Significant amounts of chromated copper arsenate (CCA) treated wood products, such as utility poles and residential construction wood, remain in service. There is increasing public concern about environmental contamination from CCA-treated wood when it is removed from service for reuse or recycling, placed in landfills or burned in commercial incinerators. In this paper, we investigated the effects of time, temperature and sodium hypochlorite concentration on chromium oxidation and extraction of chromated copper arsenate from CCA-treated wood (Type C) removed from service. Of the conditions evaluated, reaction of milled wood with sodium hypochlorite for one hour at room temperature followed by heating at 75 °C for two hours gave the highest extraction efficiency. An average of 95% Cr, 99% Cu and 96% As could be removed from CCA-treated, milled wood by this process. Most of the extracted chromium was oxidized to the hexavalent state and could therefore be recycled in a CCA treating solution. Sodium hypochlorite extracting solutions could be reused several times to extract CCA components from additional treated wood samples.  相似文献   
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