The effects of chitin and chitosan on disease incidence and severity of Fusarium yellows of celery and on populations of Fusarium oxysporum were investigated between 1994 and 1996. Field experiments were conducted at two locations with a history of severe Fusarium yellows. Disease incidence and severity were significantly reduced by pre-plant chitin amendments to soil. Chitosan applied as a root dip alone did not reduce disease incidence but significantly (P < 0.05) reduced disease severity when used with a tolerant celery cultivar. Standard soil dilution methods were used to enumerate populations of soil microflora. Chitin increased bacterial and actinomycete populations in soil in 2 of the 3 years of study. The effects of potential biocontrol agents recovered from chitin-treated plots in 1995 were studied in 1996; enriching the transplant medium with isolates of bacteria and actinomycetes 4 weeks and 1 week prior to transplanting did not alter the established equilibrium in the field, and no biocontrol effect was observed. Chitin amendments to soil or chitosan treatment of transplants did not reduce soil populations of F. oxysporum. Whether these treatments affected the F. oxysporum f. sp. apii subpopulation within the F. oxysporum population could not be determined.
Hemigossypol (HG) and 6-methoxyhemigossypol (MHG) were the major terpenoid aldehydes isolated from stem stele tissue of 6-week-old verticillium-wilt-susceptible Rowden and verticillium-wilt-resistant Seabrook Sea Island 12B2 (SBSI) cotton plants infected for 14 days with Verticillium dahliae. HG constituted 90 and 45 mol % and MHG 6 and 41 mol % of the induced terpenoid in the steles of Rowden and SBSI, respectively. No terpenoids were detected in extracts of noninfected steles.The cellular localization of terpenoids in infected and noninfected stems was studied histochemically with a SbCl3 reagent. Terpenoids first occurred in both SBSI and Rowden in scattered, usually solitary, paratracheal parenchyma cells appressed to infected xylem vessels. After extensive fungal colonization, diffusion of induced terpenoids obscured the initial, discrete sites of localization.
Subsurface drip irrigation and associated mandatory minimum tillage practices significantly reduced the incidence of lettuce drop (Sclerotinia minor) and the severity of corky root on lettuce compared with furrow irrigation and conventional tillage. Three possible mechanisms for the drip irrigation-mediated disease suppression were examined in this study: qualitative and quantitative differences in the soil microflora under furrow and subsurface drip irrigation; their antagonism and potential bio-control effects on S. minor; and the physical distribution of soil moisture and temperature relative to the two irrigation methods. To determine if the suppressive effects under subsurface drip irrigation were related to changes in soil microflora, soils were assayed for actinomycetes, bacteria, and fungi during the spring and fall seasons. The effects of the irrigation methods on microbial populations were nearly identical during both seasons. In the spring season, the total number of fungal colonies recovered on potato dextrose agar amended with rose Bengal generally was greater in soils under drip irrigation than under furrow irrigation, but no such differences were observed during the fall. Numbers of actinomycetes and bacteria were not significantly different between irrigation methods during either season. No interaction between sampling time and irrigation methods was observed for any of the microbial populations during both seasons. Thus, the significant effect of sampling time observed for actinomycete and bacterial populations during the spring was most likely not caused by the irrigation treatments. There were also no qualitative differences in the three groups of soil microflora between the irrigation treatments. Even though some fungal, actinomycete, and bacterial isolates suppressed mycelial growth of S. minor in in vitro assays, the isolates came from both subsurface drip- and furrow-irrigated soils. In in planta assays, selected isolates failed to reduce the incidence of drop in lettuce plants. The soil moisture under subsurface drip irrigation was significantly lower at all depths and distances from the bed center after an irrigation event than under furrow irrigation. The soil temperature, in contrast, was significantly higher at both 5 and 15 cm depths under drip irrigation than under furrow irrigation. The suppression of lettuce drop under subsurface drip irrigation compared with furrow irrigation is attributed to differential moisture and temperature effects rather than to changes in the soil microflora or their inhibitory effects on S. minor.
Four Verticillium dahliae isolates (V76, TS-2, PH, and V44) were used in screening four cotton cultivars (Pima S-7, Acala Prema, M-315 and Acala 44). Pima S-7 and Acala Prema gave the highest resistance reactions and Acala 44 was the most susceptible. Isolate V76 of V. dahliae was the most virulent. An interspecific cross between the resistant cv Pima S-7 (Gossypium barbadense) and the susceptible cv. Acala 44 (G. hirsutum) was made and the F 2 population phenotyped for Verticillium wilt effect. Phenotyping of plant reaction to the disease was quantified by using a set of six growth parameters (number of healthy leaves, number of nodes, leaf weight, stem weight, leaf to stem ratio, and total shoot weight) measured 3 weeks after inoculation. The F 2 phenotypic distribution of these parameters suggests that distribution is towards resistance and polygenic. Transgressive segregation also was observed. The number of healthy leaves and total shoot weight were found to be the best indicators of resistance. Results obtained in this study will be useful to quantify resistance to V. dahliae and identify the best parameters to phenotype in genetic studies.
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