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Vergara - 1976 - Physiological and morphological adaptability of ri

Vergara - 1976 - Physiological and morphological adaptability of ri

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238 ensure AND rues<br />

tial response <strong>of</strong> photosynthesis between C, <strong>and</strong> C, species to CO, concentration<br />

was mainly att<strong>ri</strong>buted to the difference in the photorespiration <strong>and</strong> diffusion<br />

resistance <strong>of</strong> stomata.<br />

The effect <strong>of</strong> CO, en<strong>ri</strong>chment <strong>of</strong> the air on growth differs with C, <strong>and</strong> C,<br />

species. Akita <strong>and</strong> Tanaka (l973b). using l6 C, species (summer plants <strong>and</strong><br />

whiter plants) <strong>and</strong> 15 C, species (summer plants). measured the effect <strong>of</strong> CO,<br />

en<strong>ri</strong>chment. These plants were treated with CO, concentration <strong>of</strong> 300 ppm.<br />

1.000 ppm. <strong>and</strong> 2,000 ppm (or 2.500 ppm) in the assimilation chambers for l8-<br />

30 days in summer. In C, species. the total dry weights in 1.000 ppm <strong>and</strong> 2.000<br />

ppm (or 2.500 ppm) xvere 1.4-4.7 times those in 300 ppm. while there were little<br />

differences among the CO, treatments in C, species. Among C, species. the<br />

effect <strong>of</strong> CO, en<strong>ri</strong>chment was greater in winter plants than in summer plants.<br />

Also, the effect <strong>of</strong> CO, en<strong>ri</strong>chment in <strong>ri</strong>ce va<strong>ri</strong>eties was 1.8-2.6 times greater<br />

than in the control. Such a remarkable difference in the CO, response between<br />

C, <strong>and</strong> C, species would p<strong>ri</strong>ma<strong>ri</strong>ly be att<strong>ri</strong>butable to the differences in the CO,<br />

response <strong>of</strong> photosynthesis between the two. The secondary cause for such a<br />

difference seems to be temperature. Lundegardh (1927) indicated that the effect<br />

<strong>of</strong> atmosphe<strong>ri</strong>c CO, en<strong>ri</strong>chment on photosynthesis <strong>of</strong> potato (C, species) was<br />

greater at a higher temperature, because the optimum temperature for photosynthesis<br />

was raised by the increase <strong>of</strong> CO, concentration. Akita et al. (1969)<br />

found that the optimum temperature for photosynthesis <strong>of</strong> C, species was<br />

scarcely affected by CO, concentration. The difference in CO, response <strong>of</strong><br />

growth between C, <strong>and</strong> C, species may be att<strong>ri</strong>buted to these CQ-tcmperaturephotosynthesis<br />

relations.<br />

Oxygen response <strong>of</strong> photosytnthesis <strong>and</strong> growth <strong>of</strong> <strong>ri</strong>ce<br />

C, species such as <strong>ri</strong>ce <strong>and</strong> wheat have a CO, release in light, that is photorespiration.<br />

which has been linked to glycolate metabolism (Zelitch. 1966) <strong>and</strong> with the<br />

presence <strong>of</strong> cell organelles called peroxisomcs (Tolbcrt ct all. 1969). C, species<br />

such as maize <strong>and</strong> sugarcane do not photorespire. Photorespiration increased<br />

proportionally to the increase <strong>of</strong> oxygen. <strong>and</strong> consequently the CO, uptake <strong>of</strong><br />

C, species was greatly influenced by oxygen concentration (Forrester et al.,<br />

1966). There is much evidence that photosynthesis <strong>and</strong> dry matter production <strong>of</strong><br />

C, species are increased remarkably by low tixygen concentration in the air.<br />

However. the drastic change in tixygen concentration from 21% to a very low<br />

level may inhibit some <strong>of</strong> the physiological functions <strong>of</strong> higher plants which have<br />

adapted to the present atmosphere.<br />

The effect <strong>of</strong> low oxygen concentration for a long pe<strong>ri</strong>od on dry matter production<br />

<strong>and</strong> growth <strong>of</strong> <strong>ri</strong>ce was reported by Akita <strong>and</strong> Tanaka (1973b). The<br />

plants were treated in assimilation chambers aerated with oxygen concentration<br />

<strong>of</strong>2l% <strong>and</strong> 3% only in daytime for 20 days from heading time to milky-dough<br />

stage. The increased dry weight in 3% taxygen was 54% greater than in 21%<br />

orwgen. This increase was mainly’ due to reduced pliotorespiration through lob<br />

oxygen concentration, because the photosynthetic capacity in a normal air just

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