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Dracaena leaf proliferosis is a newly reported disease affecting Dracaena sanderiana in Egypt. A cause and effect relationship between this disease and the fungus,Fusarium proliferatum var. minus has been established. In addition to D. sanderiana the fungus was found to be pathogenic, when tested in the laboratory, to several other members of the family Liliaceae. While the in vitro growth of the fungus is optimum at 25 °C, symptom expression is best at 30°C. Twelve fungicides were tested for their in vitro effect on fungal growth. Benlate, Rubigan, Saprol, Cercobin and Vitavax‐200 came first on the list and inhibited growth at 2.5, 12.0, 55.0, 75.0, and 94.0 μg/ml, respectively. Although, Benlate was the most effective fungicide in this respect it failed to demonstrate similar effect on disease development when applied to plants artificially inoculated with the fungus. Fungal growth was completely inhibited on PDA medium by a bacterium belonging to Bacillus sp. but when the bacterium at a concentration of 1 × 1011 cell/ml was applied 24 h before, at the same time with, or 24 h after inoculation no control of the disease was achieved. Naturally‐infected plants could, however, be freed from infection when subjected to a hot air treatment at 35 ± 5 °C during day time and 25 ± 5° C at night for 3 months.

Rubigan (a systemic fungicide) inhibited the growth of Rhizoctonia solani in vitro when used at concentrations of 6, 12 and 24 μg/ml respectively. Application of Rubigan as a soil drench significantly reduced the damping‐off incidence on cowpea (Vigna sinensis) plants. Symptoms of growth retardation appearing on cowpea plants treated with Rubigan could be mimiced using an ethylene releasing compound (Ethrel). Ethrel at 10 and 20 μl/ml added to the soil around the seeds induced severe dwarfing as evidenced from measurements of plant length, dry weight and leaf area. Gas chromatographic analysis revealed that ethylene was released either from Rubigan mixed or not with the soil. Rates of ethylene production from soils drenched with Rubigan were relatively inferiorto those produced by authentic Rubigan solutions not added to the soil. Moreover, in all cases ethylene was released at rates proportional to the Rubigan concentrations applied. Factors involved in growth retardation of Rubigan‐treated cowpea plants were discussed in the light of the possible interaction between ethylene and endogenous gibberellin levels.

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