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Vergara - 1976 - Physiological and morphological adaptability of ri

Vergara - 1976 - Physiological and morphological adaptability of ri

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RESPONSE TO DEEP WATER STRESS 309<br />

no explanation is given for this basic requirement before elongation <strong>of</strong> internodes<br />

can oecur Age is more important than height <strong>of</strong> seedlings. according to<br />

Borthakur (1971). The ability‘ to elongate apparently’ increases with age so that<br />

early sowing has a better effect on the yield as it provides better seedling resistance<br />

to flood.<br />

The emergence <strong>of</strong> paniele marks the end <strong>of</strong> internode elongation <strong>and</strong> that <strong>of</strong><br />

flood resistance. At this stage the <strong>ri</strong>ce plant can no longer elongate. <strong>and</strong> heavyi<br />

flood will mean total damage (Chou/dhury’ <strong>and</strong> Zaman, I970).<br />

Stage<br />

<strong>of</strong> leal‘ development<br />

Sato (1952) observed that the internode which is supposed to elongate as a result<br />

<strong>of</strong> submergence did so only after the leaf attached to that plant unit had ceased to<br />

elongate. This is also the sequence <strong>of</strong>devclopment under ordinary conditions. A<br />

<strong>ri</strong>ce plant unit consists <strong>of</strong> the lamina which is attached to the leaf sheath which<br />

in turn is attached on the upper end <strong>of</strong> the intcmode. The unit also includes the<br />

lateral bud located on the basal part <strong>of</strong> the internode, opposite the leaf sheath.<br />

If the energy" for elongation <strong>of</strong> a particular internode comes mainly from the<br />

leaf composing its unit. then the photosynthetic activity <strong>of</strong> that leaf is important<br />

in the elongation <strong>of</strong> the intemode—<strong>and</strong> in the survival <strong>of</strong> the plant. What then<br />

would be the effect <strong>of</strong> leaf size <strong>and</strong> leaf pruning on internode elongation‘? For a<br />

floating va<strong>ri</strong>ety’. is large leaf necessary?<br />

Temperature <strong>of</strong> water<br />

Under laboratory conditions. Kondo <strong>and</strong> Okamura (1932) reported that elongation<br />

is greatest at 25° to 30°C. At 35° to 40°C. it is retarded <strong>and</strong> the plant dies if<br />

submcrgencc is prolonged. 'l'hey noted that branching 0f the <strong>ri</strong>ce plant occurs<br />

more frequently} the higher the water temperature.<br />

Since the water temperature in the floating-<strong>ri</strong>ce areas was not reported, one<br />

cannot even estimate the natural conditions.<br />

Light <strong>and</strong> turbidity<br />

Although darkness results in internode elongation in <strong>ri</strong>ce (Takahashi <strong>and</strong><br />

Wada, 1972), the elongation when the plant is submerged is apparently limited<br />

by a factor greater than light. Elongation is more extensive in clear water than<br />

in muddy water: damage is more <strong>and</strong> sun-‘ival is less in muddy water. According<br />

to Kondo <strong>and</strong> Okamura (l934a). plants in muddy water for l0 days died. while<br />

those in elear water regained their vitality‘ when water was removed.<br />

Possibly the light received by the plant for photosynthesis is the limiting<br />

factor. This reernphasizcs the importance ot‘ the photosynthetic activity" <strong>of</strong> the<br />

leaf in the elongation <strong>of</strong> the intcmode.<br />

Duration <strong>of</strong> submergence<br />

Elongation is greater the longer the flooding time (Kondo <strong>and</strong> Okamura. 1932).<br />

Hoxvever, elongation per day is less the longer the plant remains under water.

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