Effect of Bavistin,Cotoran and Curacron on Egyptian soil fungi

Tests were conducted to determine the effects of the fungicide Bavistin (Carbendazim), the herbicide Cotoran (Fluometuron) and the insecticide Curacron on Egyptian soil fungi when applied at the recommended field dose, and four and eightfold field doses.Bavistin when added to the soil induced a regular significant inhibition of the total count of fungi by the 3 doses after 5 and 40 days and by the higher doses after 80 days. The response ofAspergillus to this fungicide was almost similar to that of the total count.Cotoran was of no significant effect on the total count of fungi after 2 days at all doses, but after 5 days the herbicide was significantly depressive at the medium and the high doses. After 80 days the effect changed into significant promotion at the field dose only.Curacron was significantly toxic to the total count of soil fungi, after the shorter and longer periods at the 3 doses.     

Selective effects of two systemic fungicides on soil fungi

BAS 317 00F was not toxic to the total count of fungi after 2 days but was regularly significantly toxic at the three doses after 5, 20 and 40 days and toxic at the low and the high doses after 80 days. In the agar medium, it was toxic to the counts of total fungi, Aspergillus, A. terreus, Rhizopus oryzae and Mucor racemosus at the high dose. Only the mycelial growth of Trichoderma viride which was significantly inhibited by the three doses when this fungicide was added to the liquid medium.Polyram-Combi induced two effects on the total population of soil fungi. One inhibitory and this was demonstrated almost regularly after 2, 10 and 40 days and the other stimulatory after 80 days of treatment with the low and the high doses. In the agar medium, this fungicide was very toxic to total fungi and to almost all fungal genera and species at the three doses. Several fungi could survive the high dose. In liquid medium, the test fungi showed variable degree of sensitivity and the most sensitive was Gliocladium roseum which was completely eradicated by the three doses.     

Effect of dithane M-45 on cellulose-decomposing fungi in Egyptian soil

The fungicide Dithane M-45 when applied to the soil was regularly and significantly toxic to the total count of fungi at all doses used (4·48, 22·4 and 44·8 mg active ingredient per kg dry soil). The toxicity was regularly increased with dose and persisted till the end of the experiment (15 weeks). When Dithane M-45 was incorporated into the agar medium all test fungi were eliminated by the high dose (24·0 ppm). The low and medium doses were tolerated by some fungi. The decay of filter paper buried in the fungicide-treated soil was significantly reduced by the high dose after 1 and 3 weeks of incubation, while the decay of filter paper treated with this fungicide and buried in untreated soil was significantly retarded by the high dose only after all experimental periods of incubation (up to 15 weeks). The growth and sporulation of nine test fungi were eliminated by the three doses of Dithane M-45 except Chaetomium globosum, Fusarium moniliforme and Trichoderma viride which could grow restrictedly at the low dose only. Production of endo-1,4β-d-glucanase and mycelial dry weight were not significantly affected by the three doses in the case of Aspergillus niger, and by the low dose in the case of Alternaria alternata, Fusarium solani and Myrothecium verrucaria. In the case of other test fungi and other doses, endo-1,4β-glucanase production and mecelial dry weight were significantly inhibited.     

Selective effects of three herbicides on the fungus flora of egyptian soil

2,4-D (2,4-dichlorophenoxyacetio acid) when applied to the soil at three doses (1.9, 7.6 and 15.2 mg per kg dry soil) had a stimulating effect on the total count of soil fungi and on several fungal species especially between 5 and 20 d after treatment. When the herbicide was incorporated in the agar medium it had a stimulating effect on the counts of total fungi, Aspergillus sp., A. niger, A.fumigatus and Fusarium app. at the low dose (6.3 ppm), but wag toxic at this dose toward Humicola grisea and Myrothecium verrucaria at the medium and high doses (25.2 and 50.4 ppm), it was toxic to the total count of fungi and to the majority of fungal species. VCS-438 [2-(3,4-dichlorophenyl)-4-methyl-l,2,4-oxadiazolidine-3,5-dione] was beneficial to the total count of fungi 2 and 5 d after soil treatment with the medium dose (8.0 mg per kg dry soil). Some fungal species could benefit from the low and the high doses (2.0 and 16.0 mg per kg dry soil) after these experimental periods. In the agar medium the counts of total fungi, Aspergillus sp., A. niger and A.fumigatus were almost significantly reduced by the three doses (6.8, 27.2 and 54.8 ppm). Planavin (4-methylsulphonyl-2,6-dinitro-N,N-dipropylaniline) was stimulating for the total count of fungi, Aspergillus, A.niger and A.ochraceus 2 and 5 d after treatment with the medium dose (8.0 mg per kg dry soil), and was also stimulating to Fusarium population at the medium dose after 2 d and at the high dose (16 mg per kg dry soil) after 20 d. In the agar medium Planavin at the low dose (6.8 ppm) was stimulating to A.terreus and inhibitory to A.nidulans and A.fumigatus. The medium and high doses (27.2 and 54.8 ppm) were generally toxic to the total count of fungi.     

Selective effect of the systemic insecticide Phosphamidon on soil,root-surface and leaf-surface fungi

Results of the effect of Phosphamidon on soil, root- and leaf-surface fungi of Vigna sinensis var. azmerly were generally inconsistent. However, there were some consistent ones. Its effect on soil, root- and leaf-surface fungi persisted till after 40 days. In soil the total count was regularly increased after 20 days by the low and medium doses and after 40 days by the high dose. In the rhizosphere, Fusarium was almost consistently activated by the three doses after 5 days of treatment and by the low dose after 20 days. In the rhizoplane, the total count of fungi was lowered by the three doses after 40 days in the two sowings. Alternaria alternata was toxicated by the three doses after several experimental periods of the two sowings in the phyllosphere and phylloplane. When this insecticide was incorporated with the agar medium, it was of no significant effect on the total count of fungi at the low and medium doses but abnormally increased the total count at the high dose. In the liquid medium, the mycelia of the test fungi were not significantly affected except that of Penicillium corylophilum which was significantly retarded by the three doses and Rhizopus stolonifer which was significantly activated by the high dose.     

Selective effects of five pesticides on soil and cotton-rhizosphere and-rhizoplane fungus flora

In two field sowings, the effect of five pesticides on soil, rhizosphere and rhizoplane fungi was tested. Ceresan and Orthocid (fungicides used as seed dressing) after 3 days were very toxic to the total count of soil fungi and to almost all fungal genera and species. After 40 days their toxicity was almost alleviated in the soil, but persisted in the rhizosphere. The herbicide VCS 438 did not significantly affect the total count of soil fungi but was initiative to the total rhizosphere fungi. Some fungal species were significantly promoted in the soil and rhizosphere and others were depressed. Dipterex (Insecticide) was promotive to the total count of soil fungi after 3 days and to some fungal species but this effect was almost alleviated after 40 days. In the rhizosphere, it exerted a promotive effect on the total count of fungi and on some fungal genera and species. Dursban (Insecticide) was of no significant effect on the total count of soil and rhizosphere fungi, but few species were significantly promoted.The rhizoplane fungi were the least sensitive, and none of the five pesticides induced a significant effect on the total count, but some species responded significantly, being either promoted or inhibited.     

Effect of the herbicide ametryn on cellulose-deeomposing fungi in Egyptian soil

Ametryn exerted a depressive effect on the total count of cellulose-decomposing fungi after 1 and 3 weeks of treatment with a high dose (54 mg active ingredient per kg dry soil), and 5 weeks after treatment with medium (27 mg) and high doses. This inhibitory effect was alleviated after 8 weeks, while after 12 weeks it was changed into promotion by a low dose (5.4 mg). When incorporated in the agar medium, this herbicide was toxic to the total count and to the counts of almost all fungal genera and species at the three doses (25, 125, 250 ppm). The decomposition of ametryn-treated calico buried in untreated soil was significantly and regularly inhibited by medium and high doses after all experimental periods. The growth and sporulation of test fungal species were partially or completely inhibited by the three doses, except,Aspergillus niger, Chaetomium globosum, andGliocladium roseum which were not affected by the low dose     

Effect of pesticides on ectomycorrhizae ofPinus sylvestris seedlings

Summary Knowledge of the effect of pesticides on the formation of forest tree mycorrhizae is important as pesticides are nowadays used in forestry. The effect of the fungicide Dithane M-45 and the herbicide Gramoxone on the growth ofPinus sylvestris L. seedlings and on the development of their mycorrhizae was studied. Investigations involved seedlings inoculated with pure cultures of mycorrhizal fungi in flasks with perlite under aseptic conditions, in Mitscherlich pots filled with perlite under semi-aseptic conditions, and on peat substrate in outdoor beds. No change in seedling growth and the mycorrhiza formation occurred when water suspension of the fungicide Dithane M-45 was used at the recommended dose. The highest rates of this fungicide had no phytotoxic effect although the growth of treated seedlings was reduced due to complete or partial inhibition of mycorrhizal formation. In contrast, even low doses of Gramoxone reduced the growth of the inoculated and non-inoculated seedlings which were more sensitive than their mycorrhizal fungi. The soil sterilization of outdoor beds with an application of a water suspension of Dithane M-45 at recommended doses reduced mycorrhizal development and seedling growth. Seedlings inoculated simultaneously with pure cultures ofSuillus granulatus showed a slightly better growth than untreated controls.     

Chromosome aberrations in spermatogonia and sperm abnormalities in Curacron-treated mice

Curacron is an organophosphorus pesticide widely used in cotton fields. In order to assay its mutagenic potential in mammalian germ cells chromosomal aberrations in spermatogonial cells and sperm abnormalities were examined in mice after Curacron treatment. For studying chromosomal aberrations mice were treated both acutely (single treatment) and subacutely (for 5 consecutive days) with 3 dose levels of Curacron, 12, 36 and 72 mg/kg. Curacron was found to produce a significant increase in structural chromosomal aberrations after acute and subacute treatments. This increase was dose-dependent. A dose-dependent inhibition in mitotic activity in spermatogonia was also found. For studying sperm abnormalities mice were treated for 5 consecutive days with 20, 40 and 60 mg/kg. Morphological sperm abnormalities increased significantly after treatment with Curacron. The increase was dose-dependent. An inhibition of 40.2% in sperm count and of 74.5% in sperm motility occurred after treatment with 60 mg/kg Curacron. These results show that Curacron has a damaging effect on spermatogonial cells as well as on sperm morphology.     

Effects of nicosulfuron on the abundance and diversity of arbuscular mycorrhizal fungi used as indicators of pesticide soil microbial toxicity

The key role of arbuscular mycorrhizal (AM) fungi in maintaining soil fertility and ecosystem functioning and their general sensitivity to pesticides make them good candidate bioindicators in pesticide soil microbial toxicity assessment. We investigated the impact of the herbicide nicosulfuron on mycorrhizal colonization and community structure of AM fungi via a pot-to-field experimental approach. This allowed the assessment of nicosulfuron toxicity (i) at extreme exposure schemes (pot experiment, Tier I) invoked by the repeated application of a range of dose rates (x0, x10, x100, x1000 the recommended dose) and (ii) under realistic exposure scenarios (x0, x1, x2, x5 the recommended dose) in the field (Tier II). In the pot experiment, the x100 and x1000 dose rates significantly reduced plant biomass, mycorrhizal colonization and AM fungal richness as determined by DGGE. This coincided with the progressive accumulation of herbicide concentrations in soil. In contrast, no effects on AM fungi were observed at the nicosulfuron dose rates tested in the field. Clone libraries showed that the majority of AM fungi belonged to the Glomus group and were sensitive to the high levels of nicosulfuron accumulated in soil at the latter culture cycles. In contrast, a Paraglomeraceae and a Glomus etunicatum ribotype were present in maize roots in all cycles and dose rates implying a tolerance to nicosulfuron-induced stress. Overall, the deleterious effects of nicosulfuron on AM fungi induced by the highest dose rates in the pot experiment could be attributed either to fungal-driven toxicity or to plant-driven effects which have subsequent implications for mycorrhizal symbiosis. We suggest that the tiered pot-to-field experimental approach followed in our study combined with classic and standardized molecular tools could provide a realistic assessment of the toxicity of pesticides onto AM fungi as potential bioindicators.     

Field and laboratory studies for evaluating the toxicity of the insecticide Reldan on soil fungi

The response of soil fungi to the insecticide Reldan (chlorpyrifos-methyl) was studied under field and laboratory conditions. The colony forming units (CFU) of fungi were determined by means of serial dilution technique after 1 day, 7, 14, and 28 days of the insecticide application in soil. The plate count data indicated that the insecticide affected the number of fungi in treated soil compared with the untreated soil; the developed colonies decreased after 1–7 days of insecticide application and then increased with increasing application time. The effect of different concentrations of insecticide on the morphological features and sporogenesis of Aspergillus flavus, Fusarium culumorum, and Drechslera biseptata was studied. Relative conidiospore formation was sharply decreased and the conidiophores were deformed in A. flavus, while F. culumorum and D. biseptata failed to produce conidiospores, although chlamydospores were formed in large numbers when cultivated on the growth medium containing insecticide.     

Time dependence of chromosomal aberrations induced in human and monkey lymphocytes by acute and fractionated exposure to 60Co

Changes in the numbers of peripheral lymphocytes with chromosome aberrations were observed in cynomolgus monkeys after fractionated or acute 60Co irradiation at the same total doses. Immediately after irradiation, the yield of dicentrics decreased when the dose was fractionated but remained constant for 20 to 80 days, depending on the dose, when irradiation was acute. Lymphopenia was greater than expected when the dose was fractionated. The kinetics of the loss of chromosome aberrations and the changes in peripheral lymphocyte count occurring in monkeys after acute irradiation were compared to those observed in accidentally irradiated men.     

Azoxystrobin and soil interactions: degradation and impact on soil bacterial and fungal communities

Aims: To provide an independent assessment of azoxystrobin effects on nontarget soil bacteria and fungi and generate some baseline information on azoxystrobin’s persistence in soil. Methods and Results: Plate based assay showed that azoxystrobin exhibited differential toxicity upon cultured fungi at different application rates. While ¹⁴C labelled isotopes experiments showed that less than 1% of azoxystrobin was mineralized, degradation studies revealed over 60% azoxystrobin breakdown over 21 days. PCR DGGE analysis of 16S and 18S rRNA genes from different soil microcosms showed that azoxystrobin had some effects on fungal community after 21 days (up to 84 days) of incubation in either light or dark soil microcosms. Light incubations increased fungal diversity while dark incubations reduced fungal diversity. Bacterial diversity was unaffected. Conclusions: Significant biotic breakdown of parent azoxystrobin occurred within 21 days even in the absence of light. Azoxystrobin under certain conditions can reduce fungal soil diversity. Significance and Impact of the Study: One of the few independent assessments of azoxystrobin (a widely used strobilurins fungicide) effects on soil fungi when used at the recommended rate. Azoxystrobin and metabolites may persist after 21 days and affect soil fungi.     

Direct application of carbendazim and propiconazole at field rates to the external mycelium of three arbuscular mycorrhizal fungi species: effect on 32P transport and succinate dehydrogenase activity

 The influence of the systemic fungicides propiconazole (Tilt 250E) and carbendazim (Bavistin) at field application rates on the functioning of three arbuscular mycorrhizal fungi was studied. Short-term fungal ³²P transport and succinate dehydrogenase (SDH) activity in external hyphae of Glomus intraradices Schenck and Smith, G. claroideum Schenck and Smith and G. invermaium Hall in symbiosis with pea (Pisum sativum L.) were measured. In the experimental system used, the hyphae grew into two root-free hyphal compartments (HCs). The fungicides were applied to each HC 24 days after sowing and ³²P was added to one HC of each pot. Four days later, the fungicide effect on fungal P transport was measured as the difference in ³²P content of treated and untreated plants. SDH activity in fungal hyphae was determined in the HCs given no ³²P. Carbendazim severely inhibited ³²P transport and SDH activity in external hyphae at an application rate of 0.5 μg g^–1 soil. The ergosterol inhibitor propiconazole affected none of these parameters. The fungicides had similar effects on all three fungal species, although P transport efficiency and SDH activity differed markedly between the fungi. Accepted: 12 December 1996     

Persistence and phytotoxicity of napropamide residues in soil

The time for 50% loss of napropamide following incorporation into a sandy loam soil in the field varied from about 130 days when applied in spring or early summer to over 200 days when applied later in the year. When left on the soil surface, up to 75% of the applied dose was lost during the first 28 days after application in June or July, whereas losses following application in November, December or January represented less than 25% of the amounts applied. These losses following surface application were closely correlated with the amounts of incoming solar radiation. First-order half-lives for degradation in nine soils incubated moist at 20°C in the laboratory varied from 72 to 150 days. They were positively correlated with the extent of herbicide adsorption by the soils and with their clay content, and negatively correlated with soil pH. Phytotoxicity to wheat and barley in the same soils in glasshouse experiments was inversely related to their organic matter content and to the extent of herbicide adsorption. Wheat was more tolerant of the herbicide than was barley. The results are discussed in terms of possible carryover problems with napropamide in some crop rotations.     

Individual and Combined Effects of Certain Pesticides on Rhizoctonia solani, Sheath Blight Pathogen of Rice

The effect of different pesticides (fungicide, herbicide and insecticide) on the mycelial growth and formation and germination of sclerotia of sheath blight pathogen of rice, Rhizoctonia solani Kühn was studied in nutrient medium and in natural soil. Among the herbicides and insecticides, fenitrothion (insecticide) and thiobencarb (herbicide) were the most effective in inhibiting the mycelial growth and sclerotial formation. These pesticides effected significant inhibition of both mycelialgrowth and sclerotial formation at 7.5 to 10μg/ml concentration while fungicides carbendazim and tolclofosmethyl effected almost complete inhibition at 2.5 μg/ml. Interestingly, a synergistic increase in the toxicity to mycelial growth, sclerotial formation and sclerotial germination was noticed when the fungicide, mancozeb and the herbicide, thiobencarb were applied at subtoxic concentration in combination. Such synergistic interactions between pesticides in a combination leading to increased toxicity suggest that under the current practice of applying fungicides, herbicides and insecticides either simultaneously or in rotation, certain combinations may help in reducing the dose of a fungicide in disease control.     

Side-Effects of Field Applications of 'Propiconazol' and 'Captafol' on the Composition of Non-target Soil Fungi in Spring Barley

The results show great seasonal variation in number and composition of the fungi isolated from the upper soil layer, especially owing to an increased isolation of primary saprophytic fungi during the late growing season. Before fungicide treatment no statistically significant difference was measured between the number of isolated fungi from the examined soils. During the treatment period significantly fewer fungi were isolated from plots treated with ‘captafol’ or ‘propiconazol’ than from the untreated plots. The differences between untreated and treated plots were not statistically significant 30 days after the last treatment. The ecotoxicological effect on the total isolated fungal flora thus seems negligible. However the fungi responded differen, tly to treatment with ‘captafol’ and ‘propiconazol’. None of the fungi were significantly affected for more than a month when treated with ‘propiconazol’. The number of primary saprophytic fungi (Cladosporium spp., Alternaria spp., Epicoccum purpurascens, and Stemphylium sp.) and Sphaeropsidales, however, was significantly reduced for more than a month when treated with ‘captafol’.     

Compensatory growth and competitive ability of an invasive weed are enhanced by soil fungi and native neighbours

Compensatory responses to herbivory by invasive weeds may foil attempts to arrest their spread with biological controls. We conducted an experiment to study the effects of defoliation and soil fungi on interactions between Centaurea melitensis , an invasive annual from Eurasia, and Nassella pulchra , a native Californian bunchgrass. Defoliation of C. melitensis reduced its final biomass in all species–fungicide treatments, except when C. melitensis was grown with both Nassella and non-treated soil fungi at the same time. In this treatment, the biomass of clipped C. melitensis plants was equal to that of unclipped plants, indicating that soil fungi and Nassella promoted a compensatory response in the weed. Overall, the biomass of C. melitensis was 44% lower when soil fungi were reduced. However, in soil not treated with fungicide, the total biomass of C. melitensis increased in the presence of Nassella , but decreased when it was grown alone. When stressed by defoliation, C. melitensis may benefit from a form of mycorrhizae-mediated parasitism through a common mycorrhizal network, or Nassella may alter the fungal community in a way that enhances the positive direct effects of soil fungi on Centaurea .     

Influence of Pesticide Use on the Natural Occurrence of Entomopathogenic Fungi in Arable Soils in the UK: Field and Laboratory Comparisons

The spectrum and abundance of entomopathogenic fungi in agricultural soil receiving different pesticide applications were evaluated . Seven small field plots within a barley crop were selected . Each plot had received a different pesticide treatment at slightly higher than the field rate each year for the previous 12-19 years . The field plots received either benomyl (fungicide) , triadimefon (fungicide) , aldicarb (insecticide) , chlorfenvinphos (insecticide) , glyphosate (herbicide) , all five of these pesticides or no pesticides at all (control) . Soil sampled from each plot was baited with Galleria mellonella larvae at either 18 or 26 C . Five species of entomopathogenic fungi infected these larvae . Beauveria bassiana was the dominant species , and the only species for which infection levels were high enough to be analyzed statistically . Significantly fewer G. mellonella larvae became infected with B. bassiana in soil treated with benomyl than in other treatments . This deleterious effect was confirmed in in vitro experiments where benomyl inhibited fungal growth significantly . Chlorfenvinphos also reduced the proportion of G. mellonella becoming infected with B. bassiana slightly (although not statistically significantly) . This effect was much greater in in vitro experiments in which chlorfenvinphos inhibited fungal growth significantly . B. bassiana- induced mortality was significantly greater in G. mellonella larvae placed in soil treated with triadimefon than in other treatments . In vitro studies , however , demonstrated that triadimefon inhibited rather than stimulated growth . A similar anomaly between field and laboratory observations was seen in the case of aldicarb . There was no significant difference in the number of G. mellonella larvae found infected with B. bassiana in soil treated with aldicarb than in the control soil . However , in the in vitro studies , aldicarb stimulated fungal growth at all concentrations except 10 times the field rate . In general , significantly fewer larvae became infected with B. bassiana at 26 C than at 18 C in all treatments . Pesticides may have a direct impact on the natural occurrence , infectivity and population dynamics of entomopathogenic fungi . They also affect other macro - and microorganisms in the soil which may interact with the ento mopathogenic fungi . In combination with climate and soil variables , these effects are difficult to separate . Although any suppression of these fungi may be detrimental to their capacity as natural enemies , this study has demonstrated that pesticides used under field conditions are unlikely either to kill all the entomopathogenic fungi present in the treated area or to limit their recolonization . It seems likely , therefore , that pesticides have the potential to be used in conjunction with mycoinsecticides in integrated pest management systems .     

水分胁迫和杀真菌剂对黄顶菊生长和抗旱性的影响

利用盆栽试验研究水分胁迫下AM真菌对黄顶菊生长和抗旱性的影响,揭示黄顶菊入侵过程中的微生物学机制。以苯菌灵为杀真菌剂,在土壤相对含水量为120%、80%、40%和20%条件下,分别设灭菌和不灭菌两种处理。结果表明,水分胁迫显著降低了黄顶菊株高、干重和主根长,而对AM真菌侵染率无显著影响。施用苯菌灵显著降低了菌根侵染率、叶片保水力、保护酶活性、可溶性糖和可溶性蛋白含量,提高了MDA含量。不灭菌处理下黄顶菊植株对土壤有效N和有效P的利用率较高,且植株全N、P含量显著高于灭菌处理,菌根贡献率随土壤相对含水量降低而逐渐提高,重度胁迫分别是渍水条件下的1.84和1.88倍。土壤水分状况和AM真菌的交互作用对黄顶菊生物量和生理指标影响显著。AM真菌共生能够促进黄顶菊根系对土壤水分和矿质营养吸收,改善植物代谢活动,提高抗旱性。实验结果为黄顶菊合理防控措施的制定提供了依据,同时作为丛枝菌根的基础性研究也具有重要的意义。