We investigated floral initiation in the long-day monocot Lolium temulentum, strain Ceres, by culturing apices explanted from photoperiodically induced plants at various times after one inductive long day onto medium with, and without, gibberellin. Apices cultured on the first day after the inductive long day usually required gibberellin in the medium to initiate floral morphogenesis while apic...

Floral induction in litchi is influenced by multiple environment cues including temperature and soil water condition. In the present study, we determined that a combined treatment consisting of 14-day drought imposed prior to exposure to 35-day low temperature (T3) significantly promoted litchi flowering relative to the low temperature alone (T2), suggesting an integrative effect of drought and...

In Arabidopsis thaliana, the initiation of flowering is carried out by four genetic pathways: gibberellin, autonomous, vernalization, and light-dependent pathways. These processes are integrated by the function of the genes FD, FE, FWA, PDF2, SOC1, and FT at the integration pathway. The integrated signal of the floral induction is transmitted to the floral meristem identity genes LFY and AP1, a...

Eucalyptus nitens (Deane & Maiden) Maiden takes at least five years to initiate flower buds from seed and is an infrequent and light flowerer. Because this behavior constitutes a major impediment to breeding programs, we examined the mechanisms controlling floral induction in E. nitens, with the long-term aim of reducing generation time and increasing seed yield. Application of paclobutrazol re...

Flowering is controlled by a variety of interrelated mechanisms. In many plants, the environment controls the production of a floral stimulus, which moves from the leaves to the shoot apex. Apices can become committed to the continuous production of flowers after the receipt of sufficient amounts of floral stimulus. However, in some plants, the commitment to continued flower production is evide...

The switch from vegetative to reproductive growth is extremely stable even if plants are only transiently exposed to environmental stimuli that trigger flowering. In the photoperiodic pathway, a mobile signal, florigen, encoded by FLOWERING LOCUS T (FT) in Arabidopsis thaliana, induces flowering. Because FT activity in leaves is not maintained after transient photoperiodic induction, the molecu...

In the last two decades the genetic and molecular research on floral development has advanced tremendously. Initially the research focused mostly on the two species of which the homeotic floral development mutants formed the basis for the ABC‐model: Arabidopsis and Antirrhinum. In recent years the importance of studying a wider range of species, especially in an ‘‘evo‐devo’’ context, has become...

In the last 15 years, knowledge of the molecular and genetic mechanisms that underlie floral induction, floral patterning, and floral organ identity has exploded. Elucidation of basic mechanisms has derived primarily from work in three dicot species: Antirrhinum majus, Arabidopsis thaliana, and Petunia hybrida. Although Antirrhinum and petunia have contributed fundamental breakthroughs to our u...

Lynn S. Adler,* Michael Wink, Melanie Distl and Amanda J. Lentz Abstract Baldwin’s critique raises some valid points. However, none invalidates our main findings of correlations between leaf and floral defences, and induction of nectar alkaloids. We believe our study successfully demonstrated linkages between leaf and floral traits, and we hope it inspires further research in multiple systems a...