In Spathiphyllum wallisii the production of doubled haploids was attempted.
Different combinations of growth regulators were tested, as well as differ
ent cultivars. The use of TDZ (0.25-1 muM) in ovary cultures of Spathiphyll
um was required. On the contrary, cytokinins were not crucial during ovule
culture; in fact, the use of a too high TDZ concentration induced diploid p
arthenogenesis in ovules of `Alfa'. The use of the imidazole fungicides IMA
, PRO or TRI during ovary culture was not critical, though they enhanced th
e swelling of ovules during ovary culture, making the isolation of the ovul
es easier. The ovule cultures yielded different plantlets. Flow cytometry a
nd AFLP-patterns showed that two doubled haploid genotypes could be obtaine
d from `Stefanie'. These plants showed a normal phenotype. We concluded tha
t the induction of homozygous Spathiphyllum through gynogenesis is possible
and is genotype dependent.