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Vergara - 1976 - Physiological and morphological adaptability of ri

Vergara - 1976 - Physiological and morphological adaptability of ri

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116 CLIMATE AND RICE<br />

about the microclirnatc <strong>of</strong> the <strong>ri</strong>ce crop has been obtained for lovrl<strong>and</strong> than for<br />

upl<strong>and</strong> <strong>ri</strong>ce. Since the physical p<strong>ri</strong>nciples governing the exchange <strong>of</strong> atmosphe<strong>ri</strong>c<br />

constituents between vegetative surfaces <strong>and</strong> the air are identical for the two<br />

ecotypes, the characte<strong>ri</strong>stics <strong>of</strong>microclimate desc<strong>ri</strong>bed here can be also applied<br />

to the microclimate <strong>of</strong> upl<strong>and</strong> <strong>ri</strong>ce.<br />

CANOPY STRUCTURE<br />

Since Murata (1961) <strong>and</strong> Tsunoda (1964) pointed out the importance <strong>of</strong>canopy'<br />

structure for increasing <strong>ri</strong>ce yield. a number <strong>of</strong> ag<strong>ri</strong>cultural techniques have<br />

been used in attempts to manipulate the display <strong>of</strong> leaves in the <strong>ri</strong>ce canopy<br />

(e.g. Tsunoda. 1964; Tanaka, 1W2; Matsushima. 1973). More recently. Tanaka<br />

et al. (1968) compared values <strong>of</strong> the light-extinction coefficient among <strong>ri</strong>ce<br />

cultivars with different yielding capacities, <strong>and</strong> found that the extinction coefficient<br />

was smaller for modern high-yielding va<strong>ri</strong>eties than for old loiv-y<strong>ri</strong>elding<br />

va<strong>ri</strong>eties.<br />

Although research led to the “plant type concept" as a guide for breeding<br />

high-yielding va<strong>ri</strong>eties <strong>of</strong> <strong>ri</strong>ce, relatively! few studies have been made <strong>of</strong> the<br />

geomet<strong>ri</strong>cal structure (architecture) <strong>of</strong> the <strong>ri</strong>ce crop. The geomet<strong>ri</strong>cal structure<br />

<strong>of</strong> plant canopies can be specified collectively by the leafarea-density’ function<br />

a(z). the leaf-inclination-density function aUBL). <strong>and</strong> the leaf-azimuth-densityr<br />

function a(j L), where z is the height above the ground or water surface, 15L. is<br />

the inclination angle <strong>of</strong>a leaf. <strong>and</strong> j L is the azimuth angle <strong>of</strong>a normal leaf.<br />

The leaf-area-density function <strong>of</strong> well-grown <strong>ri</strong>ce canopies is characte<strong>ri</strong>stic<br />

<strong>of</strong> grasses <strong>and</strong> may be represented by a curve with its maximum in the middle<br />

layer <strong>of</strong> the canopy. Figure 1 shows the change in leaf-inclination-density function<br />

<strong>of</strong> <strong>ri</strong>ce crops ivith plant development. Before heading time. most leaves are<br />

arranged in the inclination angle intewal 60°—90°. implying that <strong>ri</strong>ce crops<br />

behave like an erectophile canopy (defined by de Wit, 1965). Although cultivar<br />

1R8 retained an erectophile structure throughout the whole grov<strong>ri</strong>ng season, the<br />

canopy structure <strong>of</strong> the cultivar Manryo clearly changed from an erectophile to<br />

a plagiophile type Willi the development <strong>of</strong> flag leaves <strong>and</strong> ears. A similar trend<br />

<strong>of</strong> the leaf arrangement with the growth <strong>of</strong> plant was also observed with cultivar<br />

Hone<strong>ri</strong>ivase (Ito, 1969).<br />

In Fig. l, X represents the “leaf-area inclination index" de<strong>ri</strong>ved by Ross <strong>and</strong><br />

Ross (1969) to characte<strong>ri</strong>ze the canopy structure <strong>of</strong> plants. 1t is defined by<br />

x = 0.5[|0.|3 - g,*| + |0.3? - g2*| + |0.50 - g,,*|] (1)<br />

where g,*, g,*. <strong>and</strong> g3‘ are the leaf area fractions in each <strong>of</strong> the inclination angle<br />

intervals U°—30°, 30°—60°, <strong>and</strong> 60°—90°. respectively. Values <strong>of</strong> X in Fig. 1 clearly’<br />

denote that the IRS canopy is more erectophile than the Mamyo canopy<br />

throughout the groiving season. Stratum-bjr-stratum treatments made before<br />

<strong>and</strong> after heading revealed that the canopy structure <strong>of</strong> the cultivar Manryo

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