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1.
Processes involved in uptake and release of nitrogen dioxide from soil and building stones into the atmosphere 总被引:1,自引:0,他引:1
Atmospheric NO2 was taken up by samples of various soils and building stones. The NO2 uptake rate constants were highest in soil samples taken during the summer months. However, the NO2 uptake rate constants of the soils and building stones were not significantly correlated with any of the following variables: moisture, pH, ammonium, nitrite, or nitrate. NO2 uptake by soil and stone was not abolished by autoclaving indicating a chemical uptake process. NO2 uptake by acidic and air-dry soils and stones resulted in nearly stoichiometric reduction of NO2 to NO. This reduction was enhanced by the addition of ferrous iron and was further enhanced by incubation under 1 ppmv SO2. The results suggest that NO2 reduction may be coupled to oxidation of ferrous to ferric iron which may be reduced again by atmospheric SO2 thus regenerating the ferrous iron content of the soil or stone. Conversion of NO2 to NO was not observed in neutral or/and moist soils and stones. NO2 was also taken up by purified and sterilized quartz sand moistend with water. This uptake was enhanced by addition of humic material but not by addition of bacteria which both had been extracted from genuine soil. Under most conditions, only uptake but no release of NO2 was observed. However, NO2 was released in air-dry soils that were heated to 45–65°C, or in ammonium-fertilized soil or stone that was drying up at room temperature. Under the latter conditions mimicking field practice, the NO2 release reached rates that were similar to the NO release rates. 相似文献
2.
Rudolf Reuther 《Environmental monitoring and assessment》1994,32(3):239-258
The degree and distribution of mercury (Hg) accumulation in sediment and fish from a tributary affected by alluvial small-scale gold mining in the Madeira River/Amazon is studied, in relation to a reference site. The results obtained so far agree well with previous studies and confirm that a tremendous contamination of main food web compartments occurs in these highly exposed, but vulnerable tropical waters. An essential part of the released metallic Hg may still exist as macroscopic liquid Hg drops in the sediment. Both global (0.4 mg/kg of Hg) and local (0.1 mg/kg of Hg) background sediment values as well as safety levels for fish (0.5 mg/kg of Hg) are considerably exceeded by a factor of up to 25, 100, and 4, respectively, and give rise to serious concern, not least with regard to the formation of the very toxic monomethyl-Hg. It is further discussed that atmospheric transport and deposition of Hg in water reservoirs built for hydroelectric power generation may act as critical pathways for longterm Hg accumulation, even in unexposed riverine systems. 相似文献
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