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Vergara - 1976 - Physiological and morphological adaptability of ri

Vergara - 1976 - Physiological and morphological adaptability of ri

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RICE oaowrn m DIFFERENT ENVIRONMENTS 433<br />

The grains are the twerall results <strong>of</strong> the whole cycle <strong>of</strong> ontogenesis. llo\\=e\-'er,<br />

as the major constituents <strong>of</strong> grains are the photosynthetic products du<strong>ri</strong>ng the<br />

<strong>ri</strong>pening phase, there is no doubt that (lfjf-mflltfil‘ production du<strong>ri</strong>ng this phase is<br />

most important for grain production. It is controlled by two factors: (a) the<br />

potential ability <strong>of</strong> the population to photosynthesize (the source). <strong>and</strong> (b) the<br />

capacity <strong>of</strong> spikelets to accept the photosy/nthates (the sink) (Tanaka. 1972). The<br />

potential <strong>of</strong> the source is a function <strong>of</strong> <strong>morphological</strong> <strong>and</strong> phjvsioltigical status<br />

<strong>of</strong> the population. such as leaf area, arrangement <strong>of</strong> leaves. <strong>and</strong> their nut<strong>ri</strong>ent<br />

status. <strong>and</strong> also <strong>of</strong> the climatic condition. The status <strong>of</strong>plants can be modified by<br />

va<strong>ri</strong>etal improvements or cultural methods. but it is impossible to improve solar<br />

radiation or temperature. Thus. the climatic environment du<strong>ri</strong>ng the <strong>ri</strong>pening<br />

phase imposes the ceiling <strong>of</strong> potential <strong>of</strong> the source. The sink is composed <strong>of</strong> (a)<br />

the panicle number per unit field area, (b) the spikelct number per panic-le. (c)<br />

the field grain percentage, <strong>and</strong> (d) the siZe <strong>of</strong> individual spikelets. Among these,<br />

(a) is predominantly determined du<strong>ri</strong>ng the vegetative phase. (b) <strong>and</strong> (d) du<strong>ri</strong>ng<br />

the reproductive phase. <strong>and</strong> (c) du<strong>ri</strong>ng the reproductive phase <strong>and</strong> flowe<strong>ri</strong>ng.<br />

There are <strong>of</strong>ten negative correlations between paniele number <strong>and</strong> spikelet<br />

number per panicle. or between spikelet number per unit field area <strong>and</strong> filled<br />

grain percentage or IOOO-grain weight. due to compensation effects. Thus. the<br />

optimization <strong>of</strong> the balance among these yield components within the limit <strong>of</strong><br />

the ceiling <strong>of</strong> potential source through manipulations <strong>of</strong> the growth pattern is<br />

difficult. but indispensable in accomplishing a breakthrough in the ceiling <strong>of</strong><br />

grain yield in a given environmental condition.<br />

GROWTH<br />

PATTERNS<br />

The growth patteni is an imprecise term. but it is here taken to mean the relative<br />

strength <strong>and</strong> the sequence <strong>of</strong> the three growth phases.<br />

Types <strong>of</strong> growth patterns vary according to the combinations <strong>of</strong> va<strong>ri</strong>eties,<br />

environmental conditions. <strong>and</strong> cultural practices.<br />

The general pattern <strong>of</strong> the growth curve can be interpreted as follows: the<br />

leaf-area index (lAl) <strong>of</strong> a population <strong>of</strong> <strong>ri</strong>ce increases slowly at early grotvtlt<br />

stages, more rapidly in later stages. continues to increase until flou-‘e<strong>ri</strong>ng, <strong>and</strong><br />

then decreases due to the death <strong>of</strong> lower leaves. The crop growth rate (CGR)<br />

follows a pattern almost similar to that [)f].1AI until flowe<strong>ri</strong>ng, it is kept high<br />

even after the flowe<strong>ri</strong>ng stage because <strong>of</strong> increasing grain weight. <strong>and</strong> then it<br />

decreases. The relation between LAI <strong>and</strong> CGR is asymptotic. The CGR increases<br />

with an increase <strong>of</strong> LAI; the rate <strong>of</strong> increase <strong>of</strong> CGR decreases when<br />

LAT becomes large dtie to a decrease <strong>of</strong> the net assimilation rate (NAR) caused<br />

by the mutual shading among leaves; there is an optimum LA]. where CGR is<br />

at the maximum <strong>and</strong> above which it decreases (Tanaka et al.. 1966). An twerly<br />

vigorous increase in dry matter, consequently too fast an increase <strong>of</strong> LAI. at<br />

early growth stages is frequently’ associated with a low CGR du<strong>ri</strong>ng later growth<br />

stages, whereas a rather slow growth at early stages is associated with a high

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