Various aspects of the integration of genotype resistance and chemical control of Ascochyta blight (caused by Didymella rabiei) in chickpea were examined in field experiments from 1993 to 1999 and in greenhouse experiments. Four commercially available chickpea cultivars representing a range of resistance to D. rabiei were used. The efficacy of chemical control in a highly susceptible cultivar was significantly (P < 0.01) related to the conduciveness of the environment to the pathogen. Adequate disease suppression (>80% control) was achieved when weather supported mild epidemics, but insufficient control (<20%) was achieved when weather supported severe epidemics. The contribution of genotype resistance to disease suppression in a moderately susceptible cultivar varied from <10% when weather supported severe epidemics to approximately 60% when weather supported mild epidemics. Spraying a moderately resistant cultivar resulted in 95% control when weather supported mild epidemics, but only 65% control was achieved when weather supported severe epidemics. The existing level of resistance in a moderately resistant cultivar resulted in 70% control when weather supported severe epidemics; fungicides improved control efficacy significantly to >95%. Under mild epidemics, moderate resistance alone provided >95% control. The level of genotype resistance available in a highly resistant cultivar was sufficient to suppress the disease under all weather conditions, even without application of fungicides. The possibility of relying on postinfection rather than prophylactic application of fungicides was tested in the greenhouse and in four field experiments. Activity of the systemic fungicide tebuconazole was detected when the fungicide was applied up to 3 days postinfection, and application of tebuconazole or difenoconazole in the field as a postinfection treatment (i.e., after rain or overhead irrigation) suppressed the disease as effectively as preventive applications and required fewer sprays. In two experiments, the interaction between genotype resistance and chemical control at various amounts of irrigation applied via overhead sprinklers (as a simulation of rain) was tested. The results show that both the level of genotype resistance and the quantity of water should be taken into account in deciding whether to apply a postinfection spray.

Two nonpathogenic mutant strains 4/4 and 15/15 of Fusarium oxysporum f. sp. melonis (race 1,2) were isolated by a continuous dipinoculation technique following UV mutagenesis of the virulent wild-type isolate FOM1.2. No disease symptoms or detrimental effects were observed following inoculation of muskmelon seedlings by strain 4/4. In contrast, strain 15/15 caused mortality of susceptible cultivars although to a lesser extent than the wild-type isolate. Strain 4/4 colonized a variety of muskmelon and watermelon cultivars. In muskmelon cv. Ein Dor, seedlings were dipped in a conidial suspension of strain 4/4 and planted in medium amended with the mutant to achieve 100% colonization of roots and between 30 to 70% of the lower stem tissues 7 days after planting. Similar percent colonization of watermelon seedlings by strain 4/4 was recorded. In cross-protection experiments with muskmelon cultivars, significant reduction in seedling mortality was observed between 4/4-colonized FOM1.2. challenged plants compared with that of wild-type challenged plants alone. Similarly, strain 4/4 was able to significantly reduce mortality of watermelon seedlings caused by F. oxysporum f. sp. niveum race 2. This novel approach of generating nonpathogenic mutants for biological control in Fusarium spp. and other fungal pathogens from virulent wild-type isolates may be beneficial for control, because the mutant strains, lacking only in pathogenicity, may compete more efficiently than other biocontrol organisms against the pathogen of origin.

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Conditions affecting germination and growth of Fusarium mangiferae, causal agent of mango malformation disease, were studied in vitro. Both conidial germination and colony growth required temperatures >5 degrees C and reached a peak at 28 and 25 degrees C, respectively. A minimum 2-h wetness period was required for conidial germination, reaching a peak after 8 h of wetness. High incidence of fungal colonization in buds, predominantly the apical buds, was detected compared with inoculated leaves. The pathogen was detected in the roots of inoculated soil 19 weeks postinoculation but not in aboveground parts of the plants, and symptoms of the disease were not observed, either. Dry, malformed inflorescence debris serving as a source of inoculum caused significantly higher colonization (52 and 20%) of inoculated buds, compared with that (0%) of the untreated controls. Incidence of sampled leaf disks bearing propagules of F. mangiferae from an infected orchard peaked in June and July and decreased during the following months, whereas airborne infections on 1-month-old branches was the highest in May and June, corresponding with inoculum availability released from infected inflorescences. Colonization pattern, determined in naturally infected vegetative and woody branches, was significantly higher in node sections than in the internode sections. This study sheds light on infection dynamics, colonization patters, and the disease cycle of F. mangiferae in mango.

Alternaria leaf blight, caused by Alternaria dauci, is a major constraint to carrot production in Israel. Israeli carrot growers apply prophylactic sprays at 3- to 10-day intervals throughout the season until harvest, up to 30 sprays in a growing season. In this study, we attempted to optimize the chemical suppression of the disease, in order to reduce fungicide use. The efficacy of nine fungicides was determined in two field experiments. All fungicides reduced disease severity, but there were significant differences in efficacy among them. The most effective were difenoconazole and chlorothalonil; less effective were copper hydroxide, tebuconazole, trifloxystrobin, and mancozeb; the least effective in our experiments were flutrifol, propineb, and iprodione. The effect of the time of spray initiation on fungicide efficacy was determined in three field experiments. Qualitative (analysis of variance) and quantitative (regression) analyses of the data revealed that initiating sprays after disease onset reduced control efficacy. Thus, an action threshold model could not be developed for A. dauci in carrots. The time before harvest at which sprays could be terminated was tested in two field experiments and it was found that terminating sprays 14 days before harvest did not significantly affect the overall control efficacy. The main conclusions derived from these experiments were tested and corroborated in two additional field experiments.