Libuše Pavlová

Auxin in flowering of short-pay and long-dayChenopodium species

The fluctuation of free IAA under 16 h dark period in shoots (receptor organs of photoperiodic induction) and roots of the short-day plant (SDP)Chenopodium rubrum and in shoots of the long-day plant (LDP)Chenopodium murale is very similar. The data reflect the general adjustment of auxin level to day-length rather than changes due to floral induction. However, the shift in phasing of the circadian rhythm of flowering was accompanied by a change in the position of the’ troughs’ of free IAA levels indicating a possible relationship between the two processes. Periods of higher sensitivity to application of IAA (3. 10-4M) inhibitory to flowering have been observed both during the endogenous rhythm of flowering in the SDPC. rubrum and during induction by days of continuous illumination in the LDPC. murale. There exist common traits in the response of LDP and of SDPChenopodium to auxin treatment. Aminoethoxyvinylglycine (AVG), an inhibitor of ethylene biosynthesis, counteracted some flowering inhibitory effects of IAA when applied simultaneously with it. This suggests that auxin effects in modifying flowering might in fact be due to ethylene.

Changes in organ growth ofChenopodium rubrum due to suboptimal and multiple photoperiodic cycles with and without flowering effect

The growth changes of cotyledons, leaves, hypocotyls and roots due to photoperiodic induction in short day plantChenopodium rubrum were investigated in relation to flowering. Six-day old plants were induced by photoperiods with a different number of dark hours. We found that the degree of inhibition which occurred during induction in the growth of leaves, cotyledons and roots similarly as the stimulation of hypocotyl is proportional to the length of dark period. The photoperiods with 12, 16 and 20 dark hours bring about marked inhibition of growth and at the same time induce flowering in terminal and axillary meristems. The inhibitory effect of critical period for flowering,i.e. 8 dark hours, is not apparent in all criteria used and even the flower differentiation is retarded. The photoperiods of 4 and 6 dark hours did not affect growth and were ineffective in inducing flowering even if their number has been increased. The experiments with inductive photoperiod interrupted by light break have clearly shown that growth pattern characteristic for induced plants can be evoked in purely vegetative ones. Such statement did not exclude the possible importance of growth inhibition as a modifying factor of flower differentiation. We demonstrated that the early events of flower bud differentiation are accompanied by stimulation of leaf growth. The evaluation of growth and development of axillary buds at different nodes of insertion enabled us to quantify the photoperiodic effect and to detect the effects due to differences in dark period length not exceeding 2 hours.

The changes in the growth pattern of organs ofChenopodium rubrum photoperiodically induced to flowering

The relationship between photoperiodically changed growth of leaves, cotyledons, hypocotyl, roots and flowering has been investigated inChenopodium rubrum. It was found that all the growth characteristics recorded in leaves and cotyledons,i.e. length, area, dry weight and chlorophyll content, were inhibited during three inductive photoperiods (16 h darkness, 8 h light-SD) as compared with control plants grown under continuous illumination. Similarly, the cessation of root elongation and a decrease in root dry weight were observed. On the contrary, the elongation and dry weight of hypocotyl are stimulated by SD. The degree of the effect exerted by SD on the growth of different organs depends both on actual growth stage and the number of SD photoperiods. Increased relative rate of growth of roots and cotyledons was recorded in plants transferred after SD treatment to continuous illumination. However, this rise possesses only transitional character and the relative growth rate of treated plants equals that of control ones afterwards. The above growth changes are discussed as a possible modifying factor of floral differentiation.

Root-shoot correlation linked with photoperiodic floral induction inChenopodium rubrum L.

Inhibition of root growth was observed inChenopodium rubrum under photoperiodic conditions inducing flowering. That this inhibition is mediated by the cotyledons was shown directly by the effect of their excision, which changes the responsiveness of the roots to photoperiodic treatment. On the other hand, decapitation did not lead to such an effect. Some evidence is put forward suggesting that changes in IAA may be involved in these correlations. The existence of two different mechanisms of photoperiodic action in flowering and in root growth is proposed to explain these differences.

The effect of IAA application on endogenous rhythm of flowering in Chenopodium rubrum L.

The study deals with the effect of indol-3-ylacetic acid (IAA) on endogenous rhythm of flowering inChenopodium rubrum L. ecotype 374. Phase setting of the rhythm and length of its period were not affected, its amplitude decreased or changed insignificantly depending on the time and the site of IAA application. The intervals of significant inhibitory effect of IAA applied to apical buds terminated later than after IAA application to photoreceptive organs. The inhibitory effect did not correlate with the level of IAA uptake. Results obtained support the hypothesis that both photoreceptive organs and apical buds are the sites of inhibitory effect of applied IAA.

The transition to reproductive phase inchenopodium murale L. ecotype 197 - Early flowering long-day plant

Five days of suitable continuous light induced flowering in the majority ofChenopodium murale L. ecotype 197 plants as early as at the phase of the first pair of leaves. At the time of initiation of the 2nd to 4th pairs of leaves the capacity of plants to flower was reduced, the number of flowering plants being significantly lower under the same inductive light treatment. The capacity to flower increased again at the phase of the 5th and the 6th pairs of leaves. Inductive light treatment brought about a marked growth activation of organs present before induction, shoot apex elongation, precocious formation of new leaves and activation of axillary meristems. The course of these changes in plants of different age is demonstrated. The terminal flower developed during 5 short days following inductive light treatment. The paper shows similarities and differences between long-daymutale L. ecotype 197 and short-day C.rubrum L. ecotype 374 grown under practically uniform conditions.

Higher flower bud formation in haploid tobacco is connected with higher peroxidase/IAA-oxidase activity, lower IAA content and ethylene production

Haploid tobacco plants (cv. Samsun) form inflorescences with a larger number of flowers than diploid plants. Leaves of haploid plants were shown to have lower free IAA level (by 40 %), higher peroxidase (by 160 %) and IAA-oxidase (by 70 %) activities and produce less ethylene (by 25 %) than leaves of corresponding diploid plants. The increase of peroxidase activity in haploids was due to the increase in the activity of the cathodic isozyme which is known to have high IAA-oxidase activity. It is proposed that higher peroxidase/IAA-oxidase activity in haploid plants may take part in IAA catabolism, at least duringin vitro culture of haploid explants. Lowered IAA level and ethylene production may then be directly correlated with a larger number of flower buds; as a higher IAA level is generally considered to act as a background inhibitor of flowering.

Effect of two-or three-component PGR solution on the flowering of short-day plantChenopodium rubrum

The effect of GA3, IAA and kinetin in concentration range from 5.10-4 to 5. 10-8M, single or in combination, was tested on the flowering of short-day plant (SDP)Chenopodium rubrum (selection 374). All substances were applied as a droplet (3 (μl) of water solution before the onset of inductive photoperiod which brought about a threshold level of induction. Flowering was enhanced only in the presence of GA3 and the other two PGR decreased its effective concentration by one or two orders of magnitude. It is likely that the morphogenesis of the apical meristem was directly affected by such treatment. There is no need to assume that the ratio of employed plant growth regulators is important for the observed morphogenetic effects, but rather the actual concentrations are involved.

Organ correlations and flowering in chenopodium rubrum L.

Correlations within a shoot ofChenopodium rubrum L. ecotype 374 grown under continuous light or photoperiodic flower induction were studied using surgical treatments. Removal of a single pair of shoot organs had a variety of effects depending on position: significant changes in the number of leaf pair on the main axis or in axillary buds and in the height of shoot apices; or no effect on the parameters scored. Flowering was not affected by any of the treatments carried out. Decapitation brought about a significant increase in the number of leaf pairs in axillary buds and flowering was inhibited in 8- and 9-d old plants. Flowering was not affected in 21-d old plants. The role of shoot organ correlations, especially that of apical dominance, in regulation of flowering inC.rubrum is discussed.

Organ correlations inchenopodium rabrum l. shoots studied by Means of32P Distribution

Abstract21-day old plants ofChenopodium rubrum L. ecotype 374 were used. Organ relationships in the shoots were investigated by32P distribution, which indicated different organ correlations in plants grown in continuous light and in plants treated with flower-inducing and non-inducing dark periods. Dark periods were associated with a low32P distribution in young leaves and a high one in axillary buds. In the following light period the high32P distribution in axillary buds continued whereas the32P distribution in the leaves on the main axis increased and was similar to that in plants grown in continuous light. The high32P distribution in axillary buds was brought about by both, flower-inducing and non-inducing dark treatments. Decapitation resulted in a high32P distribution in buds, in continuous light an increased32P distribution was also found in leaves. These effects were not fully cancelled by IAA application.The results are discussed with respect to an assumption that decrease of apical dominance represents a step in a sequence of events leading to flowering.