Abeywardena, V.

De Silva, M.A.T.

George, G.D.

Coconut Research Institute Repository

Ceylon Cocon. Q. (1973) 24> 107-113 Printed in Sri Lanka NUTRITIONAL STUDIES ON INITIAL FLOWERING OF COCONUT (VAR. TYPICA). I. EFFECT OF MAGNESIUM DEFICIENCY AND Mg-P RELATIONSHIP By M. A. T. D E SILVA, V . ABEYWARDENA, G . D . GEORGE Coconut Research Institute, Lunuwila, Sri Lanka AND K . BALASUBRAMANIAM Department of Biochemistry, University of Sri Lanka, Colombo SUMMARY Analyses of fronds from bearing and non bearing adult coconut palms of identical age, showed that the latter had significantly lower levels of N,P and Mg. The relatively higher density of tender primary roots in non bearing palms has been considered to be a compensatory mechanism to absorb more magnesium from a soil known to have a marginal magnesium status. However the observed deficiency of both magnesium and phosphorus in fronds of non bearing palms, viewed in relation to the observed accumulation of phosphorus in their roots, seems to indicate that the translocation of phosphorus from root to shoot could be adversely affected when the supply level of magnesium is low. P has been shown to have a profound influence on initial flowering of coconuts. Delayed flowering in these coconut palms at Bandirippuwa, Sri Lanka is thus attributed to an induced lower­ing of P in fronds, caused by a lower uptake of magnesium by roots. Coconut palms (var. typica) are known to flower in about five to eight years after trans­planting in the field. A delay in initial flowering is often observed in poorly managed planta­tions where palms may take as much as twelve years to commence flowering. Abeywardena (1961) found that the frequency of initial flowering in coconut (var. typica) did not follow the normal distribution, ft was suggested that the positive skewness in the dis­tribution curve of initial flowering was an inherent feature in a coconut plantation grown under sub-optimal conditions, caused probably by competition for nutrients. The present work was initiated to examine some of the nutritional factors which may affect initial flowering in coconut. MATERIALS AND METHODS Materials for this investigation were taken in August 1971 from an eleven year old coconut plantation at Bandirippuwa Estate, Lunuwila, Sri Lanka. The plantation which covered about 8 hectares, received annually a fertilizer mixture containing 2.3 kg of ammonium sulphate, 0.9 kg of saphos phosphate and 1.4 kg of muriate of potash in a dosage of 4.5 kg per palm. At the time of the investigation approximately 20 percent of the palms of this block had not commenced flowering. 107 108 M. A. T. DE SILVA V. ABEYWARDENA G. D. GEORGE AND K. BALASUBRAMANIAM The soil in this area is known to have a marginal magnesium status ,since extracts of the soil with 10-2 molar solutions of calcium chloride gave values less than 20 x 10-3 for the molar .Mg : Ca ratio suggested as critical by Nethsinghe (1963). However, striking foliar symptoms were not evident. Leaf samples The 14th frond counting basipetally from the youngest fully opened leaf (1st leaf) was sampled from 10 bearing and 10 non bearing palms for the determination of major mineral nutrients. Twenty leaflets from the mid region of each frond were removed, and after separating the midribs, the middle third of the laminae were prepared for analysis. Root counts and root samples. The bases of 10 bearing and 10 non bearing palms were excavated to expose the rooting zone. The mature (lignified) and tender primary roots in the top 5.0 cm strip of the rooting zone on the bole of each palm were counted. Samples of root tips 2.0 cm in length, were also taken from the tender roots of these palms, and analysed for calcium, magnesium and phosphorus. Earlier studies on the distribution of mineral nutrients in young roots showed that the highest concentration of each nutrient was present in the 2.0 cm length from the tip, indicating that this was the region of highest absorption (De Silva, unpublished). Analytical methods. Nitrogen was determined by Kjeldhal's method, phosphorus by the vanado—molybdate colorimetric method and potassium by flame photometry. Calcium and magnesium were esti­mated in ashed extracts with-EDTA after separating phosphorus with zirconyl chloride (Der-derian, 1961). RESULTS Nitrogen, phosphorus, potassium, calcium and magnesium in the laminae (14th frond) of bearing and non bearing coconut palms are expressed as percentages in Table I (a), and as total amounts in Table I (b). The data in Table I (a) show that the percentages of magnesium and phosphorus in non bearing palms were significantly lower than in bearing palms, while there were no significant differences in nitrogen, potassium and calcium percentages between the two groups. It may also be noted that the magnesium levels in leaves of non bearing palms are well below the "critical level" of 0.300 per cent suggested by Fremond et al. (1966), while phosphorus concentrations lie in the neighbourhood of the suggested critical level of 0.120 percent. On the other hand, in leaves of bearing palms, magnesium concentrations are marginal, while phosphorus concentra­tions may be considered to be optimal. The same data when expressed as the total amounts present in laminae (Table 1 (b), showed that in addition to magnesium and phosphorus, nitrogen was also significantly low (P—0.05) in the non bearing palms. In Table 2 is summarised the distribution of mature and tender primary roots in the top 5.0 cm of the rooting zone on the bole of bearing and non bearing palms. A distinct feature of non bearing palms is the presence of fewer mature roots and a significantly greater number of tender primaries. The ratio of mature to tender roots is significantly higher in the bearing th*n in the non bearing trees. The analytical data of root tips (Table 3) sampled from tender primary roots of the two categories of plants show that in non bearing palms, phosphorus and calcium were significantly higher than in those of the bearing palms. Therefore in these plants the phosphate status in roots was the reverse of that found in leaves. Although the magnesium contents in the root tips of bearing palms were generally higher than in those of non bearing palms, the differences were not statistically significant. Table 1 (a) N,P,K, Ca and Mg in laminae of the 14th frond of bearing and nan bearing coconut palms (percentage oven—dry natter). N P K Ca Mg Mean (%) 2.657 0.1736*** 1.678 0.2540 0.1695** Bearing Range* 2 .28— 0.1569- 1 .08- 0 .1158- 0 .1166-3 .00 0.1889 2 .09 0.3297 0.3276 Mean(%) 2.462 0.1461 1.566 0.2601 0.0973 Non' bearing Range 1 .69- 0 .1159- 1 .23- 0 .1788- 0 .0259-3.05 0.1739 1.99 0.3491 0.1774 **—Significant at P—0.01 ***—Significant at P--0.001 TaMe 1 (b). Total amount in grams of the various elements present in the laminae of the 14th frond of bearing and non-bearing coconut palms. N P K Ca Mg Bearing 36.969* 2.428*** 23.830 3.535 2.326*** Non bearing 29.330 1.734 18.250 3.081 1.1338 •Significant at P=0.05 "Significant at P=0.01 ***Significant at P = 0 . 0 0 l Table 2. Distribution of mature and tender primary roots on the top 5.0 cm. of flic rooting zone or bole in beariog and nonbearing coconut palms. {Mean ofW palms in each category) Tender roots Mature roots Mature/Tender ratio Bearing palms 48.7*** 186.7 5.45** Non bearing palms 81.9 148.4 1.78 ** Significant at P=0 .01 *** Significant at P=0.001 Table 3. Phosphorus, calcium and magnesium contents in root tips of bearing and nonbearing palms expressed as contents per 100 g of the oven dry sample. P Ca Mg * Bearing palms Mean : 0.5533** 0.0862*** 0.1462 Range : 0 .5028- 0 .0583- 0 .1089-0.6922 0.1071 0.2194 Non bearing palms Mean : 0.6579 0.0918 0.1299 Range : 0 .5407- 0 .0625- 0 .0853-0.7770 0.1323 0.2498 ** Significant at P=0 .01 *** Significant at P=0 .001 Fig. I. Effects of N, P and K. on initial flowering of coconut palms(var. typica), at Ratmalagara Research Station, Madampe. Data extracted partly from unpublished records and partly from 'Reports of the Soil Chemist' appearing in Annual Reports of the Coconut Research Institute of Ceylon, for years 1954—59. mt* * N - P K ^ E x p t - ' P o t t u k u l a i f l t t R i u i a T c f t Station Fig. 2. Effects of N and P on initial flowering of coconut palms (var. typica), at Pottukulama Research Station. Data extracted partly from unpublished records and partly from 'Reports of the Soil Chemist' appearing in Annual Reports of the Coconut Research Institute of Ceylon, for years 1965 and 1966. NUTRITIONAL STUDIES ON INITIAL FLOWERING OF COCONUT 113 The results presented in Figs. 1 and 2 are from long term fertilizer experiments carried out by the Coconut Research Institute of Sri Lanka. Fig. I depicts the influence of nitrogen, phosphorus and potassium fertilizerson initial flowering in coconut growing ona phosphate de­ficient soil (bicarbonate extractable P—4.6 ppm) at Madampe in north—west of Sri Lanka. Fig. 2 shows the influence of phosphorus on initial flowering of coconut growing on a soil at Pottukulama in north—west of Sri Lanka whose bicarbonate extractable phosphorus was 8.8 ppm. Fig. 1 clearly shows the stimulation of initial flowering of coconut palms by phosphorus. DISCUSSION In the present study it is noted that magnesium is relatively low in the fronds as well as in the roots of non bearing palms when compared with those of bearing palms. On the other hand phosphorus has been shown to be low in the fronds and high in the roots in non bearing palms when compared to those of bearing palms. It was likely therefore that due to a deficiency of magnesium (probably on account of low availability), movement of absorbed phosphorus from root to shoot in coconut palms was adversely affected causing in effect a "physiological" lowering of phosphorus in leaves and its accumulation in the roots. Such an inference would lend support to the "Carrier Theory" of Truog et al. (1947). They found that when the supply of magnesium to pea plants grown in water culture experiments was increased, a corresponding increase was observed of both magnesium and phosphorus in pea seeds; and this occurred re­gardless of the change in the supply level of phosphorus. Such observations led them to believe that magnesium could function as a "carrier" for phosphorus. However, Hewitt (1962) con­tended that this behaviour was due mainly to the almost universal importance of magnesium in the enzyme systems which are involved in all aspects of phosphorus metabolism. As mentioned earlier, the bearing and non bearing palms selected for this study were from the same plot and received the identical fertilizer mixture containing N, P and K. Although these palms had a comparable background, the two categories behaved differently in respect of magnesium nutrition. The reason for this is not clear, but it is likely that a genetic factor was involved in which the non bearing palm behaved as a "magnesium—susceptible" genotype. The ratio of mature to tender roots was higher in bearing than in non bearing palms. The greater number of tender primary roots on non bearing palms was probably a compensatory mechanism to absorb more magnesium from a soil which was known tohave a marginal magnesium status. Apparently this adaptation did not have the desired effect, since magnesium levels in fronds on non bearing palms remained low. This decrease in magnesium resulted in the lower­ing of phosphorus in leaves of non bearing palms. The information obtained from Figs. I and 2 clearly demonstrate the signal importance of phosphorus for the production of flowers in coconut palms. It may thus be concluded that a secondary deficiency of phosphorus in leaves induced by a primary deficiency of magnesium was a factor responsible for delayed production of reproductive structures in the plants under investi­gation. As referred to earlier, apart from magnesium and phosphorus, the total nitrogen content in leaves of non bearing palms was also low. In collateral investigations, Balasubramaniam et al. (1974) have shown that a derangement in carbohydrate metabolism probably leads to this low nitrogen content in leaves of non bearing palms. REFERENCES Abcywardena, V. 1961 Ceylon Cocon. Q 12,132. Balasubramaniam, K., Sothary, R.D. & De Silva, M.A.T. 1974 Ceylon Cocon. Q. (To be published) Dc Silva, M.A.T. (Unpublished). Dcrderian, M.D. 1961 Analyl. Chem. 33, 1796. Fremond, Y., Ziller, R. & De Nuce De Lamothe, M. 1966 The Coconut Palm. International Potash Institute. Berne, Switzerland. Hewitt, E.J. 1963. Plant Physiology ed.F.C. Steward, Vol. 3, p. 175 London: Academic Press. Nethsinghe, D.A. 1963. Ceylon Cocon. Q. 14, 8. Truog E.. Goates R.J., Gerjoff, G.L. & Berger, K.C. 1947. Soil Sci. 63,19. 

Nutritional studies on initial flowering of coconut (Var. Typica) i effect of magnesium deficiency and Mg-P relationship

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Nutritional studies on initial flowering of coconut (Var. Typica) i effect of magnesium deficiency and Mg-P relationship

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