Male flower buds were differentiated in mid-July 2007; the first flowers opened in early August and by 28 August most of the male flowers were senescent.
Different species of flowers are differentiated enough that, like faces, they can be told apart by running them through a series of filters made to highlight certain features.
Once all female flowers are differentiated, and there is no flower drop, we assume that their numbers will remain stable until the onset of flower drop, with possible record variations due to sampling.
The expression level reached a peak at stage 3 in O. barthii and remained at the same level at stage 4 (young flowers with differentiated organs).
Stage 1, Inflorescence meristem stage, after initiation of primary branch (i.e. rachis and primary branch meristems); stage 2, early branching stage (panicle with elongated primary and higher order branch development); stage 3, late branching stage (i.e. panicle with elongated primary and secondary branches); stage 4, young flowers with differentiated organs.
In phase D (Fig. 4e-h) the most intense fluorescence signal was mostly localized in the differentiated parts of the flower: sepals, petals and surrounding tissues, all of them also intensely stained with DAPI (Fig. 4f and 4g).
A consistently differentiated trait between these populations is flowering time saline origin genotypes flower earlier in non-saline field conditions, on all field-collected soils, and under both saline and non-saline treatments.
We show that flowering time is differentiated between saline and non-saline populations and may allow salt stress escape.
The other cluster was formed by roots and flowers, which were differentiated in 28% of the comparisons and were both highly differentiated from shoot apex and pollen.
The post-hoc tests revealed that some periods (325 362 ms and 476 498 ms) at T6 were indeed differentiated significantly in both comparisons of faces vs. flowers and faces vs. cars.
