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Vergara - 1976 - Physiological and morphological adaptability of ri

Vergara - 1976 - Physiological and morphological adaptability of ri

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168 CLINLATE AND RICE<br />

Top growth<br />

Top growth <strong>of</strong> <strong>ri</strong>ce plants after transplanting is, in general. linearly accelerated by<br />

raising average temperature from approximately 18°C to 33°C (Ueki, 1966;<br />

Place et al.. 1971'. Sato. 1972a; Chamura <strong>and</strong> Honma, 1973; Osada. Takahashi.<br />

Dhammanuvong, Sasiprapa. <strong>and</strong> Guntharatom. 1973; Yoshida. 1973). Above<br />

<strong>and</strong> below this range. the growth notably decreases. Water temperature is<br />

much more significant than air temperature for early growth <strong>and</strong> development<br />

<strong>of</strong> lowl<strong>and</strong> <strong>ri</strong>ce (Matsushima et al., 1964b. 1966. 1968a. 1968b; Hoshino et a1..<br />

1969). This is because the growing points <strong>of</strong> the plants are under ivater. The<br />

effects <strong>of</strong> water temperature on the early growth <strong>of</strong> <strong>ri</strong>ce plants are basically the<br />

same as those mentioned above (Matsushima et a1, 1964b, 1968b). Sato (l972a)<br />

found that dry matter production was the largest under a day-night temperature<br />

regime <strong>of</strong> 30°—25°C for No<strong>ri</strong>n l7. <strong>and</strong> at 25°-20°C for 1R8; leaf area per plant<br />

was the largest at 30°—25°C for both va<strong>ri</strong>eties; thus. the temperature <strong>of</strong> 35°—30°C<br />

was overly high for the growth <strong>of</strong>either japonica or indica va<strong>ri</strong>eties.<br />

Sasaki (1927) reported that the elongation <strong>of</strong> <strong>ri</strong>ee leaves increased with <strong>ri</strong>sing<br />

temperature from 17° to 31°C; thence it tended to decrease <strong>and</strong> practically<br />

ceased at 45°C. The lower limit <strong>of</strong> temperature for <strong>ri</strong>ce leaf elongation was<br />

estimated at 7°—8°C (Sasaki. 1927). at 10°C (Aimi. 1965) <strong>and</strong> at 12°C (Tanaka<br />

<strong>and</strong> Munakata, 1974). Oda <strong>and</strong> Honma (1963) reported that the velocity <strong>of</strong> leaf<br />

emergence was greater at ivanner conditions. <strong>and</strong> this hastened heading accompanying<br />

the decrease in leaf number.<br />

Kaneda <strong>and</strong> Beachell (1974) surveyed the types <strong>of</strong> cold injury <strong>of</strong> <strong>ri</strong>ce plants in<br />

more than 10 count<strong>ri</strong>es. For cold inju<strong>ri</strong>es at vegetative growth stages, failure in<br />

germination <strong>and</strong> slow seedling growth were observed in almost all count<strong>ri</strong>es<br />

surveyed; stunting <strong>and</strong> discoloration <strong>of</strong> leaves ivere reported in more than half<br />

<strong>of</strong> them. Crennination <strong>and</strong> early seedling growth have been discussed earlier in<br />

this review Seedling discoloration is commonly seen in indica va<strong>ri</strong>eties grown<br />

under low temperatures. The discoloration is tisually va<strong>ri</strong>ous degrees <strong>of</strong> yellmving<br />

<strong>of</strong> leaves; sometimes white specks on leaves <strong>and</strong> white b<strong>and</strong>s on sheaths, or<br />

whitening <strong>of</strong> entire leaves are observed. At tille<strong>ri</strong>ng stage. the yellotving occurs<br />

on lower leaves. Stunting occurs at tille<strong>ri</strong>ng stage in boro crops. Yellowing <strong>of</strong><br />

leaves was observed also in japoniea va<strong>ri</strong>eties grown at 9° <strong>and</strong> 13°C (Chamura<br />

<strong>and</strong> Honma. 1973).<br />

Tille<strong>ri</strong>ng<br />

There is disagreement among reported data about the effect <strong>of</strong> temperature on<br />

tille<strong>ri</strong>ng. First, a number <strong>of</strong> researchers (Oka. 1955; lakahashi et al._ 1955;<br />

llasegawa. 1959'. Nagai <strong>and</strong> Matsushita. 1963; Matsushima et a1. 1964b‘.<br />

Kakizaki. 1965; Charnura <strong>and</strong> Honma, 1973; Yoshida. 1973) reported that<br />

tille<strong>ri</strong>ng increased with <strong>ri</strong>sing temperature in a range from approximately 15° to<br />

33°C. Among them, Oka <strong>and</strong> Takahashi et a1. indicated that the tille<strong>ri</strong>ng pe<strong>ri</strong>od<br />

was shortened by the optimal temperatures for tille<strong>ri</strong>ng differentiation. <strong>and</strong><br />

thence the final number <strong>of</strong>tillers decreased with <strong>ri</strong>sing temperature. Matsnshima

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