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Yoshida - 1981 - Fundamentals of Rice Crop Science

Yoshida - 1981 - Fundamentals of Rice Crop Science

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198 FUNDAMENTALS OF RICE CROP SCIENCE<br />

change is expressed as (McCree 1974):<br />

dW/dt = D – N, (5.7)<br />

where D = daytime net total <strong>of</strong> CO 2 taken up by the plant and<br />

N = night total <strong>of</strong> CO 2 evolved by the plant.<br />

When dW/dt is expressed per unit <strong>of</strong> ground area (g dry matter/m 2 per day or<br />

week), it is called crop growth rate (CGR). The crop growth rate is used as a<br />

measure <strong>of</strong> primary productivity <strong>of</strong> crops in the field.<br />

5.1.2. Characteristics <strong>of</strong> rice photosynthesis<br />

<strong>Rice</strong> is generally believed to have a C-3 photosynthetic pathway (Ishii et al 1977b).<br />

There is, however, a report that suggests the operation <strong>of</strong> both C-3 and C-4<br />

pathways in a salt-tolerant indica variety (Hegde and Joshi 1974).<br />

As a C-3 plant, rice has a high CO 2 compensation point, exhibits photorespiration,<br />

and lacks bundle sheath chloroplasts (Table 5.2). Compared with other C-3<br />

species, however, rice has a relatively higher net photosynthetic rate per unit <strong>of</strong><br />

leaf area. Within Oryza sativa, indica rices have a higher optimum temperature<br />

than japonica rices. Early papers on rice photosynthesis reported a leaf photosynthetic<br />

rate <strong>of</strong> 10–20 mg CO 2 /dm 2 per hour, while recent papers indicate a rate<br />

<strong>of</strong> 40–50 mg CO 2 /dm 2 per hour. This difference could be attributed primarily to<br />

improvements in the measuring technique (<strong>Yoshida</strong> and Shioya 1976). In early<br />

studies on rice photosynthesis, the CO 2 exchange rate was measured by enclosing<br />

several cut leaves in aplastic chamber. Later studies, however, use an intact leaf.<br />

The photorespiration rate increases with increasing light intensity, but the rate<br />

<strong>of</strong> photorespiration relative to the rate <strong>of</strong> CO 2 fixation is higher at lower light<br />

intensities. At light intensities lower than 10 klx, photorespiration accounts for<br />

70–90% <strong>of</strong> CO 2 fixation. At 40 klx, it accounts for 40% (Ishii et al 1977c).<br />

At the moment, lowering the oxygen concentration in air is the most convenient<br />

means <strong>of</strong> reducing photorespiration. A group <strong>of</strong> plant growth regulators can also<br />

reduce photorespiration and increase photosynthetic activity (Zelitch 1979).<br />

When rice was grown in a low-oxygen atmosphere, both photosynthesis and dry<br />

matter production increased; grain yield decreased due to an increased percentage<br />

<strong>of</strong> unfertile grains. The percentage spikelet fertility <strong>of</strong> Tangin Bozu and Hoyoku<br />

varieties decreased from 86 and 74% in the 21% O 2 atmosphere to 22 and 46% in<br />

the 3% O 2 atmosphere, respectively (Akita and Tanaka 1973). Thus, inhibiting<br />

photorespiration by lowering the oxygen concentration did not increase the grain<br />

yield.<br />

5.1.3. <strong>Crop</strong> photosynthesis<br />

<strong>Crop</strong> photosynthesis in the field is primarily determined by incident solar radiation,<br />

photosynthetic rate per unit leaf area, leaf area index, and leaf orientation.

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