Regulation of gynophore elongation and fructification in the peanut arachis hypogaea L.

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Date

2001

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Uniiversity of California

Abstract

The regulation of peanut gynophore elongation and the fructification process were studied using Spanish bunch variety grown under constant temperature (26.5°C), photoperiod (12 hr) and relative humidity (ca 90%) in a growth chamber. The experimental material consisted of tagged flowers or gynophores continuously made available by replanting. A technique utilizing the floral morphology was devised to study effects of exogenous growth substances applied independently or in combinations on the induction of IM activity (gynophore initiation) in the absence of fertilization and syngamy. Growth substances are able to evoke IM activity thus substituting for the syngamic stimulus. The effect of GA was dose-dependent suggesting that it may be a critical factor in gynophore initiation, however, a mixture of GA, IAA and BA was more effective than individual or combined effects of BA and IAA. Morphactin showed stimulatory effect on IM activity. When applied to fertilized flowers, CEPA and Ag+ ions inhibited IM activity, the latter by postponing hypantha abscission. In the absence of exogenous auxin, gynophores initiated without fertilization failed to show geotropic curvatures denoting the role of auxin in mediating normal geotropism. Growth substance initiated gynophores were incapable of fructification and their limited elongation was suggestive of the necessity of proembryonic secondary stimuli for these processes. Gibberellic acid promoted while other tested growth substances i.e. IAA, BA, CEPA, TIBA, CCC and morphactin inhibited intact gynophore elongation. Ovule removal stagnated elongation partially overcome by GA confirming the role of the proembryos for sustained IM activity. Auxin or BA inhibited GA- promoted intact gynophore elongation depending on gynophore age auxin being more inhibitory on the younger gynophores being least responsive irrespective of concentration. When applied to flowers at anthesis, morphactin transiently inhibited geotropic curvature development but copiously altered gynophore trajectory.94. The size and activity of the IM zone decreases towards the ovule base with progressive gynophore lengthening. Gibberellic acid affects elongation by increasing length of IM cells whose elongation is basipetally polarized. inverse The relationship between fructification depth and gynophore length is attributed the to decreasing size and activity together with internal differentiation of the IM zone with age. A definition of peanut 'fruit-set' is suggested as being at time of IM induction (i.e. gynophore initiation phase of fruit development) and the gynophore as a physiologically unique young fruit. The observation that ovule removal delayed but did not prevent curvature development ot excised gynophores suggested the perceptive and responsive nature of the IM to geotropic stimulus. Morphactin enhanced elongation of excised gynophores for all concentrations with optima at 0.1 and 10 ppm and effectively altered geotropic curvature even at 0.1 to I ppm. Higher morphactin concentrations relationship rendered between gynophores the ageotropic. anti-geotropic effect There and was an inverse growth stimulation. Morphactin, however, failed to stimulate growth in the presence of auxin which partially reversed its effects on geotropism. Auxin inhibited excised gynophore elongation for all concentrations but progressively reduced the degree of curvature. The effect of morphactin and auxin on elongation are further evidence on gynophore physiological similarity to roots and the regulation of geotropic curvature by auxin. Tri-iodobenzoic acid (TIBA) and BA inhibited elongation and curvature with increasing concentration, TIBA more drastically than BA. While GA stimulated growth without appreciable effects on curvature, it partially reversed concentration dependent ancymidol-induced inhibition of these parameters. The fructification process, characterized as simultaneous cessation of gynophore elongation and ovule enlargement is enhanced by growth inhibitors,95. morphactin, IAA and CEPA while GA postponed it by perpetuating IM activity with resultant greater fructification depths. The inhibitory effects of Ag+ions, an anti-ethylene agent on fructification suggest the involvement of ethylene in regulating this process. Depth perception by gynophores is attributed to endogenous hormones acting on the IM. Pericarp growth which is mainly by water retention by the tissue precedes that of the seed but the latter accumulates most of the dry weight in the course of growth. Benzyladenine (BA) enhances fruit growth by increasing water content and kernel dry matter. Distal seed growth was greatly improved by BA treatment by increasing its sink strength which resulted in the reduction of pops and single seededness.

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Keywords

Gynophore, Elongation, Peanut Arachis, Hypogaea L.

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