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EN
Samples of five species of wild edible mushrooms, growing in the vicinity of Warsaw, were analyzed in order to determine discrimination factors (DF) for 137Cs and 40K in their caps and stipes. The obtained DF values range from 0.80 to 2.87, and seem to be characteristic of each species. A brief discussion of the observed phenomenon is presented.
EN
As a result of the rapid development of nanotechnology and increasing application of nanoproducts in many areas of everyday life, there is a growing risk of production of nanowastes potentially dangerous for the environment. This makes it necessary to investigate the accumulation and toxicity of nanoparticles (NPs) at different trophic levels. In the studies neutron activation was applied for the investigation of iron (II,III) oxide nanoparticle (Fe3O4-NPs) accumulation by Lepidium sativum and Pisum sativum L. Plants were cultivated on growth medium contaminated with different concentrations (0.01-10 mmolźL-1) of Fe3O4-NPs. For the identification of the presence of Fe3O4-NPs in plant tissues gamma spectrometry following iron oxide (II,III) nanoparticles irradiation was applied. Both plant species were found to accumulate iron (II,III) oxide nanoparticles. The highest content of NPs was found in plant roots, reaching 40 g/kg for Pisum sativum L. More than 90% of accumulated NPs were found in roots. Accumulation of Fe3O4-NPs was found to depend on the concentration of nanostructures in the growth medium. The transfer factor for Lepidium sativum roots and shoots and Pisum sativum L. shoots decreased with increasing NP concentration in the medium; for Pisum sativum L. roots the tendency was reversed. Neutron activation of nanoparticles was shown to be a powerful tool for tracing the environmental fate of NPs and their uptake and accumulation in organisms.
EN
A model species of saprophytic fungus, king oyster mushroom (Pleurotus eryngii), was cultivated on barley substrate supplied with [Pt(NH3)4](NO3)2, under well defined conditions. The samples of the collected fruiting bodies were digested and analyzed for total platinum content by means of ICP-MS. The results proved that platinum is not accumulated in the fruitbodies of Pleurotus eryngii for a wide range of Pt concentrations in the culture substrate (100 1000 ppb Pt in 50 ml of water solution added to ca. 450 g of hydrated barley seeds per container). Observable levels of Pt were only found in the fruitbodies obtained from the medium contaminated with 10000 ppb (10 ppm) platinum solution. This demonstrates significant difference in the effectiveness of platinum extraction in fungi and plants, which are capable to accumulate platinum even when supplied at lower concentration (<500 ppb). It also shows different physiological pathways of platinum and other elements which are easily accumulated in the fruitbodies of the same species.
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