Pseudothecia containing abundant ascospores of Mycosphaerella brassicicola were produced in vitro on Brussels sprout decoction agar at 15ЊC under a 16-hour photoperiod of different light regimes. Spermogonia containing spermatia were also produced on the decoction agar. Ascospores were released when cultures were misted with SDW and placed under continuous light. Germination of ascospores was highest between 20ЊC and 25ЊC and spores remained viable at relative humidities above 93·5%. Exposure of ascospores to 55% relative humidity for 24 h reduced their germination to 75%. A polyclonal antiserum raised against whole ascospores was used to detect, by immunofluorescence, the ascospore and mycelial wall of M. brassicicola, following reaction with anti-rabbit IgG FITC conjugate. Autofluorescence of spore and mycelial components of other fungal species could be eliminated using the counterstains Evan's blue and eriochrome black at 0·2% and 0·5%, respectively, in phosphate buffered saline (pH 7·2). A procedure was developed to detect, by immunofluorescence, ascospores of M. brassicicola on artificially inoculated Melinex spore tape. Coating of the spore tape with bovine serum albumin provided a suitable support medium and blocking agent for detection of ascospores in the field. The potential use of the system for selective detection of ascospores of M. brassicicola in infected crops of vegetable brassicas in the presence of other ascosporic fungi is discussed.

During March and April of 1993 and 1994, surveys on the incidence and severity of cashew powdery mildew (Oidium anacardii) were conducted in the Newala, Mtwara, Nachingwea and Tunduru areas of southern Tanzania to determine the variation in perennation between localities. Only immature cashew shoots, panicles and fruit can be infected by O. anacardii conidia. Cashew trees at sites in each district were assessed for shoot and panicle production and cashew powdery mildew. Survival of O. anacardii between seasons, in any area, was determined by the degree of production of shoots that were within the canopy and by the incidence of infection. Immature shoots produced from the main branches within the tree canopy were the main source of active powdery mildew in all districts; trees in the Newala district had the highest numbers of infected immature shoots in comparison with survey sites in the other areas. During the 1994 cashew‐growing season (June–August), powdery mildew developed more rapidly and affected more shoots on the inside of the tree canopy than on the outside. Germination of conidia was reduced after aqueous suspension for 3 h. Germination on cashew leaves submerged under 2 mm of water was not affected. Appressorial and hyphal formation by germinating conidia on leaves decreased with increasing duration under water. Germination of conidia on glass slides at 100% r.h. was higher at 25 and 30°C than at 15°C and there was no germination at 35°C.