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11.
Measurements of nitrogen dioxide, nitrous and nitric acids as well as ozone were made using newly developed instrumentation onboard the research vessel Aegeon in the Aegean Sea between 25th–29th July 2000. Typical nitrogen dioxide concentrations observed aboard the boat were 4–6 ppb (v/v) with a broad maximum of 20–30 ppb (v/v). Ozone concentrations typically ranged between 40 and 80 ppb (v/v). Mixing ratios of both nitric and nitrous acids in the ambient air of the Aegean Sea were mainly below 50 ppt (v/v). The data also showed a number of short pollution episodes with rapid changes in the concentration of reactive nitrogen compounds [nitrogen dioxide maximum up to 164 ppb (v/v), nitric acid maximum up to 12 ppb (v/v), nitrous acid maximum up to 2.7 ppb (v/v)] and ozone [maximum up to 88 ppb (v/v)]. These episodes were correlated with pollution plumes originating from boats upwind, at short distance, from the R/V Aegeon. The measurements revealed the importance of nitrous and nitric acids for the transport of nitrogen to marine biota in busy ship lanes.  相似文献   
12.
Nitrous oxide emission from some English and Welsh rivers and estuaries   总被引:4,自引:0,他引:4  
Nutrient and N2O concentrations in the water columns were measured seasonally over a full salinity range in the nutrified rivers Colne, Stour, Orwell, Deben, Trent, Ouse and Humber and their estuaries on the east coast of England between August 2001 and May 2002, and in the oligotrophic rivers Conwy, Dovey and Mawddach in North and West Wales between August 2002 and May 2003. Nutrient and N2O concentrations in the nutrified English rivers and estuaries were much higher than those in the Welsh rivers. N2O concentrations and % saturation in the estuaries were significantly correlated with nitrate, nitrite and ammonium concentrations in the water. The strongest correlation was with nitrite (r2 = 0.56, p < 0.01), suggesting that nitrite was the most significant factor among the different nutrients in regulating N2O concentration in the estuaries. N2O concentrations in the English rivers and estuaries were supersaturated throughout the year with annual averages from 186.9 to 992.9%, indicating that these rivers and estuaries were sources of atmospheric N2O, whereas in the Welsh rivers N2O concentrations were much lower with annual averages from 113.6 to 137.4% saturation. Although the estuarine area in the Colne was almost the same as that in the Conwy, the annual N2O emission from the Colne was much higher (937498 mol N yr–1) than in the Conwy (23020 mol N yr–1). On the east coast, riverine emissions of N2O were only 0.5–12.5% of the total emission from rivers and estuaries. Thus rivers were negligible, but estuaries were significant contributors to the UK N2O inventory.  相似文献   
13.
The short- and long-term fixation of 14CO2 by Phaeodactylum tricornutum was studied using methods of fractionation that allowed examination of all the products labelled with 14C. There was no doubt that the major pathway of CO2 fixation was into 3-phosphoglycerate, but there was also significant incorporation by -carboxylation by means of phosphoenol-pyruvate carboxylase and transamination into aspartate. At short time intervals (10 sec), 90% of the radioactive products found were accounted for by 3-phosphoglycerate and aspartate. The lipids associated with the photosynthetic apparatus contained a high proportion of the 14C fixed, which at 60 sec was located mainly in the carbohydrate portion of the lipids. At 30 and 300 min, the chlorophylls, carotenoids and the long-chain fatty acids were heavily labelled with 14C. The monogalacto-diglycerides, the digalacto-diglycerides and the sulpholipids each had a characteristic long-chain fatty acid composition. The cell proteins and a reserve polysaccharide were also labelled with 14C at short time intervals and increased their radioactivity in a linear fashion up to the longest period studied, 300 min. The activity of the enzymes ribulose diphosphate carboxylase and phosphoenolpyruvate carboxylase was sufficient to account for the pattern of fixation found.  相似文献   
14.
Background arctic aerosol properties generally observed during the summer were studied at Ny-Ålesund, Svalbard in a six-week campaign where the aerosol size distribution and chemical composition were measured. The results presented here demonstrate the marked difference between the background arctic aerosol composition in comparison to the aged aerosol arriving in the area by long-range transport from southern latitudes. It is found that sulphate is the major water-soluble component of background aerosol followed by sea salt. Aged aerosol arriving in the Arctic from polluted areas is recognised by an increase in black carbon and in the refractory aerosol fraction.  相似文献   
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