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Polyacrylamide gel electrophoresis (PAGE) was used to study the polymorphism of esterases in Allium cepa L. and A. fistulosum L. Two varieties of each species, an A. fistulosum × A. cepa interspecific F1 hybrid, and (A. fistulosum × A. cepa) hybrid derivatives were analyzed for determination of banding patterns upon staining with α- and β-napthyl acetate substrates of esterase. Complex band patterns were observed. In total, 10 bands were detected between A. cepa and A. fistulosum — five inA. cepa, six in A. fistulosum with only one band common to both species. With the exception of one band unique to A. fistulosum which appeared only when stained with α-substrate, extracts of both A. cepa and A. fistulosum leaf tissue exhibited the same bands when stained with both α- and β-substrates. Bands stained with the different systems are distinguished by color: α-substrate always appeared black, while bands stained to β-substrate are always red. Esterase bands were assigned into 5 presumptive loci of four zones of activity with according to the migration distance of the bands from the front, color of each band upon staining with α- and β-substrates, and segregation observed in crosses and hybrid derivatives. Esterase enzymes detected in this study appear to be monomeric. Polymorphisms were identified between A. cepa and A. fistulosum by esterase banding patterns. Esterase enzymes provide an additional marker in monitoring introgression of foreign germplasm in interspecific onion breeding.

Onion varieties from Northern-Europe, Eastern-Europe, Southern-Europe and the U.S. including populations, inbreds, synthetics and clones were tested for their gynogenesis ability for three years: 1993-1995. Embryos were induced in Petri dishes using in vitro culture of flower buds. Embryo rate, regeneration rate, survival rate, embryo quality and ploidy level of regenerants are described. Important genotype and variety effects are pointed out; embryo production and plant regeneration ranged from 0 to 17% and from 0 to 11% of inoculated flowers, respectively. Highest results were obtained with inbreds and synthetics for embryo production as well as for plant regeneration. Populations expressed various responses which were generally low. Geographic origin and year effects were covered by the effects of genetic structure of varieties and specific genotype of donor plant. Among regenerants, 80% were haploid and 13% were spontaneous diploid. No relation has been found between general quality and ploidy level of regenerants. The choice of plant material for successful gynogenesis in onion is discussed.

The morphological variation and the isozymic polymorphism in 19 asparagus accessions currently used in cultivation and breeding are described. Moreover 2 wild populations from Turkey were added in the isozymic study. Characters of ramification height permit to separate accessions usually cultivated for white asparagus and accessions usually cultivated for green asparagus. Starch and polyacrylamide gel electrophoresis was realized to assay 7 enzyme systems. 29 polymorphic bands were taken into account in the study. Four accessions show specific bands for glutamate oxaloacetate transaminase, shikimate dehydrogenase and alcohol dehydrogenase. In particular, the two populations from Turkey and one population traditionally cultivated in local area of Spain are well differentiated from the remaining accessions. Accessions from the United States representing different selections are relatively well separated from each other.