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In incubation experiments the microbiological equilibrium of two sandy soils was unsettled using captan in a dose which considerably influenced fungi. The reduction of the fungal community contributed to an intensive multiplication of the bacteria detectable by the cultural method, particularly of the number of their eutrophic forms. However, the changes in the discussed ecotrophic group of bacteria were not accompanied by an increase in the total number of the soil bacteria community detectable with the help of the microscope and consisted for the most part from oligotrophic bacteria. Moreover, there was a continous declining tendency and overall microbial activity of the soil was in most instances reduced. All the described effects were intensified by the addition of fresh organic matter.
The paper describes a field experiment with the application of two biocides: oxytetracycline that reduced bacteria and captan that reduced soil fungi. The purpose of the experiment was to investigate the response of enchytraeid species to the changes of the abundance and activity of the microbial community as part of their food resources. The following variables were recorded: the biomass of microorganisms by the PLFA method, the rate of cellulose decomposition and the numbers and species composition of enchytraeids. No relationship was found between enchytraeids and abundance of microorganisms, but numbers of animals were correlated with changes in soil cellulolytic activity. Both biocides, even the non toxic oxytetracycline, reduced the diversity (H’) of enchytraeid community by increasing the proportion of dominant species. It is suggested that biocides reduced the functional diversity of microorganisms, and this factor had an effect on the enchytraeid populations. The animals responded to the treatment and their community became predominated by the species probably with a broad food spectrum.
The mutagenic activity of captan and captafol was tested using Ames stzaiiis and strains showing an SOS response. Captafol was mutagenic in S. typhimurium strain TA102 (uvr+) and captan in strain TA104 (uvrB). Both captan and captafol elicit damages in DNA recognized by correndonuclease U, as shown by the repair teat, and induced the SOS repair system in E. coli PQ37 (uvrA) strain. Only captafol induced the SOS system in PQ35 (uvr+). The lack of induction of p-galactesidaac at nonpermissive temperature in E. coli MD332 (dnaCs uvrA) strain showed that neither chemical was able to produce DNA breaks. In V79 Chinese hamster fibroblasts higher induction of c-mitosis by captafol than by captan (22% and 15% over th* control, respectively) was accompanied by a higher decrease in nonprotein sulfhydryl groups, mainly GSH (41% and 77%, respectively). The content of protein sulfhydryl groups was decreased by either fungicide to a similar extent.
Studies on disappearance of captan, trifloxistrobin, cyprodinil and fludioxonil residues in fruits and leaves after their application against diseases were carried out. The initial deposits of cyprodinil and fludioxonil in fruits were on the levels 0.236±0.064 and 0.294±0.039 mg/kg, respectively, and disappeared more quickly than those of captan. However their residues during harvest were still significantly higher than 0.01 mg/kg. Quite similar behaviour was found to be in the case of trifloxistrobin initial deposits. Results of the studies indicated that the apples could not be used for baby food production.
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