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31.
32.
Actinolite, anthophyllite, amosite, chrysotile and tremolite varieties of asbestos from Indian mines were analysed for their chemical composition. Significant differences were found as compared with the composition of corresponding foreign varieties. The significance of this in relation to their possible toxic effects and the need for toxicological work with Indian varieties are discussed.  相似文献   
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The monthly concentrations of NO2, NOx, SO2 and O3 measured by a passive sampler from February 2003 to January 2004 showed that the air pollution during the winter season in Kathmandu valley was higher than the summer season. The O3 level was found the highest during April, May and June due to strong radiation. The hourly concentrations of NO2, NOx, O3 and suspended particulate matter(SPM) were also measured by automatic instruments on December 2003. Temperature at the height of 60 m and 400 m at Raniban Mountain in the northwest of Kathmandu valley was measured on February 2001 in the winter season and the average potential temperature gradient was estimated from observed temperature. Wind speed was also measured at the department of hydrology, airport section, from 18 February to 6 March 2001. It was found that the stable layer and the calm condition in the atmosphere strongly affected the appearance of the maximum concentrations of NO2 and SPM in the morning, and that the unstable layer and the windy condition in the atmosphere was considerably relevant to the decrease of air pollution concentrations at daytime. The emission amounts of NOx, HCs and total suspended particle(TSP) from transport sector in 2003 were estimated from the increasing rate of vehicles on the basis of the emission amounts in 1993 to be 3751 t/a, 30570 t/a and 1317 t/a, respectively. The diurnal concentrations in 2003 calculated by the two-layers box model reproduced the characteristics of air pollution in Kathmandu valley such as the maximum value of O3 and its time, the maximum value of NO in the morning, and the decrease of NO and NO2 at daytime. The comparison with the concentrations in 1993 calculated suggested that the main cause of air pollution was the emission from transport sector.  相似文献   
35.
Carbon Management in Agricultural Soils   总被引:11,自引:0,他引:11  
World soils have been a major source of enrichment of atmospheric concentration of CO2 ever since the dawn of settled agriculture, about 10,000 years ago. Historic emission of soil C is estimated at 78 ± 12 Pg out of the total terrestrial emission of 136 ± 55 Pg, and post-industrial fossil fuel emission of 270 ± 30 Pg. Most soils in agricultural ecosystems have lost 50 to 75% of their antecedent soil C pool, with the magnitude of loss ranging from 30 to 60 Mg C/ha. The depletion of soil organic carbon (SOC) pool is exacerbated by soil drainage, plowing, removal of crop residue, biomass burning, subsistence or low-input agriculture, and soil degradation by erosion and other processes. The magnitude of soil C depletion is high in coarse-textured soils (e.g., sandy texture, excessive internal drainage, low activity clays and poor aggregation), prone to soil erosion and other degradative processes. Thus, most agricultural soils contain soil C pool below their ecological potential. Adoption of recommend management practices (e.g., no-till farming with crop residue mulch, incorporation of forages in the rotation cycle, maintaining a positive nutrient balance, use of manure and other biosolids), conversion of agriculturally marginal soils to a perennial land use, and restoration of degraded soils and wetlands can enhance the SOC pool. Cultivation of peatlands and harvesting of peatland moss must be strongly discouraged, and restoration of degraded soils and ecosystems encouraged especially in developing countries. The rate of SOC sequestration is 300 to 500 Kg C/ha/yr under intensive agricultural practices, and 0.8 to 1.0 Mg/ha/yr through restoration of wetlands. In soils with severe depletion of SOC pool, the rate of SOC sequestration with adoption of restorative measures which add a considerable amount of biomass to the soil, and irrigated farming may be 1.0 to 1.5 Mg/ha/yr. Principal mechanisms of soil C sequestration include aggregation, high humification rate of biosolids applied to soil, deep transfer into the sub-soil horizons, formation of secondary carbonates and leaching of bicarbonates into the ground water. The rate of formation of secondary carbonates may be 10 to 15 Kg/ha/yr, and the rate of leaching of bicarbonates with good quality irrigation water may be 0.25 to 1.0 Mg C/ha/yr. The global potential of soil C sequestration is 0.6 to 1.2 Pg C/yr which can off-set about 15% of the fossil fuel emissions.  相似文献   
36.
The hepatoprotective potential of a herbal mixture was evaluated against CCl4 induced liver injury in Swiss albino mice. Liv 52, a commercially available polyherbal hepatoprotective drug was evaluated for comparison. The potential toxicity of the above herbal hepatoprotective agents was also compared. It was observed that there was a reduction in the enzyme biomarkers (Aspartate and Alanine Transaminase) of liver injury in the herbal mixture treated groups, which was similar to the reduction initiated by Liv 52. An increase in glutathione was observed in the herbal mixture treated groups and it was assumed that the herbal mixture protects the liver by virtue of its antioxidant nature along with high regeneration initiation potential. From the study it is also concluded that the herbal mixture is safer than Liv 52.  相似文献   
37.

Background, aim, and scope

Primitive wax refining techniques had resulted in almost 50,000 tonnes of acidic oily sludge (pH 1–3) being accumulated inside the Digboi refinery premises in Assam state, northeast India. A novel yeast species Candida digboiensis TERI ASN6 was obtained that could degrade the acidic petroleum hydrocarbons at pH 3 under laboratory conditions. The aim of this study was to evaluate the degradation potential of this strain under laboratory and field conditions.

Materials and methods

The ability of TERI ASN6 to degrade the hydrocarbons found in the acidic oily sludge was established by gravimetry and gas chromatography–mass spectroscopy. Following this, a feasibility study was done, on site, to study various treatments for the remediation of the acidic sludge. Among the treatments, the application of C. digboiensis TERI ASN6 with nutrients showed the highest degradation of the acidic oily sludge. This treatment was then selected for the full-scale bioremediation study conducted on site, inside the refinery premises.

Results

The novel yeast strain TERI ASN6 could degrade 40 mg of eicosane in 50 ml of minimal salts medium in 10 days and 72% of heneicosane in 192 h at pH 3. The degradation of alkanes yielded monocarboxylic acid intermediates while the polycyclic aromatic hydrocarbon pyrene found in the acidic oily sludge yielded the oxygenated intermediate pyrenol. In the feasibility study, the application of TERI ASN6 with nutrients showed a reduction of solvent extractable total petroleum hydrocarbon (TPH) from 160 to 28.81 g kg?1 soil as compared to a TPH reduction from 183.85 to 151.10 g kg?1 soil in the untreated control in 135 days. The full-scale bioremediation study in a 3,280-m2 area in the refinery showed a reduction of TPH from 184.06 to 7.96 g kg?1 soil in 175 days.

Discussion

Degradation of petroleum hydrocarbons by microbes is a well-known phenomenon, but most microbes are unable to withstand the low pH conditions found in Digboi refinery. The strain C. digboiensis could efficiently degrade the acidic oily sludge on site because of its robust nature, probably acquired by prolonged exposure to the contaminants.

Conclusions

This study establishes the potential of novel yeast strain to bioremediate hydrocarbons at low pH under field conditions.

Recommendations and perspectives

Acidic oily sludge is a potential environmental hazard. The components of the oily sludge are toxic and carcinogenic, and the acidity of the sludge further increases this problem. These results establish that the novel yeast strain C. digboiensis was able to degrade hydrocarbons at low pH and can therefore be used for bioremediating soils that have been contaminated by acidic hydrocarbon wastes generated by other methods as well.  相似文献   
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Environmental Science and Pollution Research - Mining and extraction of stones and minerals play a significant role in many countries economic growth in the world. The production of dolomite...  相似文献   
40.
Soil analyses were conducted on home lawns across diverse ecoregions of the U.S. to determine the soil organic carbon (SOC) sink capacity of turfgrass soils. Establishment of lawns sequestered SOC over time. Due to variations in ecoregions, sequestration rates varied among sites from 0.9 Mg carbon (C) ha?1 year?1 to 5.4 Mg C ha?1 year?1. Potential SOC sink capacity also varied among sites ranging from 20.8 ± 1.0–96.3 ± 6.0 Mg C ha?1. Average sequestration rate and sink capacity for all sites sampled were 2.8 ± 0.3 Mg C ha?1 year?1 and 45.8 ± 3.5 Mg C ha?1, respectively. Additionally, the hidden carbon costs (HCC) due to lawn mowing (189.7 kg Ce (carbon equivalent) ha?1 year?1) and fertilizer use (63.6 kg Ce ha?1 year?1) for all sites totaled 254.3 kg Ce ha?1 year?1. Considering home lawn SOC sink capacity and HCC, mean home lawn sequestration was completely negated 184 years post establishment. The potential SOC sink capacity of home lawns in the U.S. was estimated at 496.3 Tg C, with HCC of between 2,504.1 Gg Ce year?1 under low management regimes and 7551.4 Gg Ce year?1 under high management. This leads to a carbon-positive system for between 66 and 199 years in U.S. home lawns. More efficient and reduction of C-intensive maintenance practices could increase the overall sequestration longevity of home lawns and improve their climate change mitigation potential.  相似文献   
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