M. Anzidei et al., Organogenesis and somatic embryogenesis in Foeniculum vulgare: histological observations of developing embryogenic callus, PL CELL TIS, 61(1), 2000, pp. 69-79
Different NAA plus kinetin or BA combinations were tested on Francia Pernod
fennel seedlings for callus induction and plant regeneration. Callogenesis
from hypocotyls was obtained in all auxin/cytokinin-containing media. The
organogenic response was observed especially in presence of NAA plus kineti
n. The highest frequency of shoot regeneration was found when the auxin and
kinetin were used at a 1:1 ratio. Moreover, a prolonged culture period inc
reased shoot formation. Somatic embryogenesis was tested on several fennel
populations. The results gave evidence of the genotypic importance. Two dif
ferent protocols were used for somatic embryo induction. Using the first pr
otocol among the different fennel genotypes tested, only Francia Pernod sho
wed embryogenic capacity. In this case, from a primary non-embryogenic call
us cultured for 12 months in presence of 2,4-D, an embryogenic secondary ca
llus was produced. When transferred to the medium without 2,4-D (agarized o
r liquid), this gave embryogenic plants in high frequency. As far as the se
cond embryogenic method is concerned, secondary embryogenic callus develope
d only in the presence of 2,4-D plus kinetin in Francia Pernod genotype. Th
ereafter, the replacement of those growth regulators by GA(3) into the medi
um greatly increased the somatic embryo development, especially in 'Francia
Pernod', but also in 'Aboca erbe' callus, a population with a very poor em
bryogenic capacity. In Francia Pernod, the primary and secondary (embryogen
ic) calli showed different morphological and histological responses, either
when the secondary callus was induced by 2,4-D alone or by 2,4-D plus kine
tin. Ontogenetic processes leading to somatic embryo formation are describe
d in this context.