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Petal formation in steel targets was observed at 60° obliquity.
The sepal petal formation stage was an important stage which regulated endogenous hormones in the ovary locule formation.
The axial fibres placed nearer to outer surface leads to more number of petal formation, leading to a stable crushing mechanism.
The correlation showed that, during sepal petal formation stage, the ovary locule numbers were positively correlated with GA3, GA3/IAA, and GA3/ABA, and were negatively correlated with IAA and ABA.
This paper investigates the influence of fibre orientation and stacking sequence on the petal formation and specific energy absorption (SEA) of four and six-ply, 0°/90° glass/polyester composite cylindrical shells under axial compression.
Petal formation occurred in the aluminum targets and four petals were generally formed in each plate, however, the size of the upper two petals decreased and that of the lower two petals increased with increase in target obliquity.
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In Iberis amara, unequal petal pair formation correlates with a stronger expression of the CYC2 clade gene IaTCP1 in the smaller, adaxial petals.
However, in model plants, typical B gene loss of function mutants display a second whorl of sepals instead of petals and the formation of carpeloid stamens.
A significantly enhanced occurrence of genes involved in cell wall organization and modification processes in adaxial petals implies that the formation of smaller, adaxial petals is a result of an earlier onset of cell expansion, compared to the large, abaxial petals.
The identity of other genes involved in this process, especially those related to petal and stamen primordia formation, is an interesting subject for future research.
Gene categories associated with 'Molecular Function' were also found to be highly represented during flower formation and petal senescence in safflower, carnation, orchids and wallflower [ 41, 51– 51].
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