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Products based on different strains of entomopathogenic fungi are now being used in Integrated Pest Management (IPM) programs. Compatibility studies of chemical and biological control agents are necessary to be able to give proper recommendations for their integrated use. The effect of three insecticides based on imidacloprid, spinosad and abamectin, and three fungicides based on chlorothalonil, azoxystrobin and thiophanate-methyl on the activity of the following entomopathogenic fungi: Metarhizium anisopliae (Metschn.) sensu lato, Beauveria bassiana (Bals.-Criv.) Vuill., Acremonium sp. was tested under laboratory conditions. Tests of the influence of the pesticides on growth and production of conidia were performed. From this study, we concluded that all tested insecticides can be applied together with fungus B. bassiana products in IPM programs. They even stimulate sporulation of this fungus at the recommended dose, 0.5 of the recommended dose and 1.5 times the recommended dose. In the case of fungicides we observed inhibition of growth and sporulation of B. bassiana and reduction of growth and sporulation of other species of fungi.
The present paper presents the results of long-term observations of differences in growth and morphology of colonies of C. fraxinea isolated from ash stems with symptoms of dieback and the results of studies on effects of temperature on growth and morphology of colonies in vitro. Thirty randomly chosen C. fraxinea cultures, originating from six Forest Districts in southern and northern Poland, viz. Andrychów, Gryfice, Kańczuga, Lębork, Miechów and Mircze, were included in the temperature assay. Colony growth and morphology were evaluated in vitro, on malt extract agar. Two replicates of each isolate were incubated at 5, 10, 15, 20, 25 and 30oC in darkness. Colonies of C. fraxinea isolated from necrotic stem tissues of diseased ash trees differed greatly in colour, structure, growth rate, presence of sectors and stromata as well as the intensity of conidial sporulation. Colony characters were often lost in further sub-cultures grown on the same medium. Colonies of C. fraxinea grew at 5-25oC in vitro. Three isolates still grew, though slowly, at 30oC. The optimum temperature for growth was 20oC. Among 30 isolates tested, five grew most quickly at 25oC and four at 15oC. Differences among colony diameters recorded at 5, 10, 15, 20 and 30oC were statistically significant, while differences at 15 and 25oC were not. At some temperatures, statistically significant differences in growth rate were related to the origin of the isolates. There were three main colony colour types. Temperature was the main factor affecting colony morphology in vitro. The formation of sectors was observed in 36% of colonies, pseudoparenchymatous stromata in 10.4% of colonies, and white crystalline substances in 53.3% of colonies. The results of in vitro observations were used for discussion of the effects of temperature on growth and activity of C. fraxinea in vivo.
New biological properties of selected insect peptides are presented. The subjects of the investigation included insect oostatic peptides, like Neb-colloostatin (I) and Neb-TMOF(II), and/or insect peptides with antiviral or antitumor activity, such as alloferon (III) and its analogues modified at position 1 of the peptide chain. In the study was also included the oligopeptide Any-GS (VII) and its truncated analogues. The peptides were tested for antimicrobial activity on a series of bacterial species, antiviral activity against Human Herpes Virus type 1 (HHV-1) in vitro using a Vero cell line, and the growth and development of plant pathogens Phoma narcissi and Botrytis tulipae. The results of the biological investigations indicate that among the peptides investigated, compounds VII and IX inhibit the growth of plant pathogens P. narcissi and B. tulipae, whereas compounds I and II stimulate the mycelium growth of the aforementioned pathogens. Other peptides show slow antimicrobial activity but do not inhibit the replication of HHV-1 in Vero cells.
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