Haploid induction in onion can, to date, be induced only via gynogenesis by
culturing unfertilized flowers, ovaries or ovules. The process of haploid
embryo induction has been macroscopically well studied, but only limited da
ta exist from microscopic examination of ovule development status at the in
oculation stage and of the origin of gynogenic embryos. Microscopic studies
were carried out using individual donor plants with relatively high embryo
induction frequencies (45.9 embryos formed per 100 flowers, on average, fo
r 2 years). Ovaries from flower bud culture were fixed at 1 week intervals
up to the 7th week of culture. These were compared with pollinated ovaries
at 1 or 2 weeks after pollination. In total, 1428 unfertilized embryo sacs
were examined. The results indicate that, at the time of inoculation, ovule
s within ovaries 2.0-3.0 mm. in diameter contained two- or four-nucleate em
bryo sacs in the smallest ovaries to mature embryo sacs in the largest ovar
ies. It seems likely that the embryos are actually induced from ovaries cul
tured at the immature stage. After 1 or 2 weeks in culture, the egg apparat
us primarily consisted of distinctly enlarged synergids and the egg cell, w
hich was often detached from the micropylar pole. But free nuclear endosper
m was also formed. From the 2nd to 7th week in culture, formation of haploi
d embryos (from globular to the almost mature cylindrical stage) was detect
ed in 5.7% of the ovules. Their origin, for several reasons, was most likel
y the egg cell. In addition, ovules containing endosperm only (3.6%) and ov
ules containing the egg apparatus (0.5%) or both endosperm and embryo (0.4%
) were detected. This observation is probably unique and has not yet been r
eported in other species studied.