Partial resistance to downy mildew ( Plasmopara halstedii) and to black stem (Phoma macdonaldii) in sunflower were investigated under natural field infection and a controlled growth chamber respectively. Genetic control for resistance to the diseases was determined in recombinant inbred lines (RILs) and their two parents, 'PAC-2' and 'RHA-266.' The experiments were undertaken in a randomized complete block design with two replications, in a field severely infected by downy mildew and in a controlled growth chamber with plants inoculated with an agressive French isolate of P. macdonaldii. Each replication consisted of three rows, 4.6-m long, giving 48 plants per RIL or parent in the field and 15 plants in the growth chamber. Genetic variability was observed among the RILs for resistance to both diseases. When 10% of the selected RILs were compared with the mean of the two parents genetic gain was significant for partial resistance to the diseases. Four putative QTLs for resistance to downy mildew on linkage groups 1, 9 and 17 were detected using composite interval mapping. The QTLs explained 54.9% of the total phenotypic variance. Major QTLs ( dmr1-1 and dmr1-2) for resistance were found on linkage group 1 with up to 31% of the phenotypic variability explained by two peaks. QTL analysis of resistance to black stem showed seven QTLs on linkage groups 3, 6, 8, 9, 11, 15 and 17. The detected QTLs together explain 92% of the phenotypic variation of the trait. Crosses between RILs contrasted for their resistance to downy mildew and black stem, and exhibiting molecular polymorphism in detected QTLs, will be made in order to focus more-precisely on the genomic region of interest.

Two programmes to investigate the inheritance of resistance to black stem in sunflowers were undertaken in a controlled-environment growth chamber. In the first, an experiment was performed using a randomized complete block design with 24 lines, six male-sterile (A lines), six maintainers (B lines), six restorers (R lines) and their six F 1 hybrids in six replications. Each treatment consisted of 12 seedlings. Twelve-day-old seedlings were inoculated with a suspension of pycniospores, and 7 days later the two cotyledon petioles of each seedling were scored on a 1±9 scale for the percentage of necrotic area. Some alloplasmic lines (which have the same nucleus and different cytoplasms) gave a significant cytoplasmic effect for improved partial resistance to the disease. Deviation of F 1 hybrids from the mean of the parent values was significant for partial resistance to Phoma macdonaldii in three of the six F 1 hybrids. Two further experiments with eight lines (resistant and susceptible) at the fifth leaf-pair and flowering stages were carried out under the same conditions. At both growth stages the previous classification of lines at the seedling stage was confirmed. In the second programme, five male-sterile sunflower lines were crossed with five fertility-restorers in a factorial mating design. The 10 inbred lines and their 25 F 1 hybrids were studied in two successive experiments under the same conditions and with the same experimental design and isolate of Phoma as in the seedling-stage experiment in the first programme. Analysis of variance showed that male-sterile and restorer lines possessed general combining abilities, and also that specific combining abilities of F 1 hybrids were significant. The estimates of general combining ability for partial resistance were significant in AS617A, AS618A and AS614R inbred lines. These lines are available for developing F 1 hybrids with improved resistance to Phoma in sunflower-breeding programmes.

Isolates of Drechslera teres that cause net or spot-type symptoms on barley {Hordeum vulgare) were collected in 1986 and 1987 from fields in different regions of France. Variations in pathogenicity were to all isolates except R5 and S5. The Ethiopian cultivar Cl 5791, previously reported to be resistant, was susceptible to the R5 and S5 biotypes. There was a high correlation coefficient between the classification of cultivars for resistance to D. teres f. sp. teres and D. teres f. sp. maeulata. A method for conserving the virulence of the isolates on straw is evaluated. The virulence level of the isolates was the same after 4 years of storage using this method.