Yoshida - 1981 - Fundamentals of Rice Crop Science
Yoshida - 1981 - Fundamentals of Rice Crop Science
Yoshida - 1981 - Fundamentals of Rice Crop Science
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132 FUNDAMENTALS OF RICE CROP SCIENCE<br />
where N is number <strong>of</strong> tillers, t is time, and r is a constant. The solution for the<br />
equation 3.14 is:<br />
r = log e N 2 – log e N 1 2.303 (log 10 N 2 – log 10 N 1 )<br />
=<br />
t 2 – t 1 t 2 – t 1<br />
(3.15)<br />
The constant r is called the relative tillering rate (RTR) on the analogy <strong>of</strong> the<br />
relative growth rate. Equation 3.14 can be rewritten as:<br />
dN 1<br />
RTR = × (3.16)<br />
dt N<br />
Thus, RTR can be considered the mean tillering rate per tiller and used as a<br />
quantitative measure for the relationship between mineral nutrition and tillering.<br />
As shown in Figure 3.8a and b, the RTR is closely correlated with nitrogen,<br />
phosphorus, and potassium content in the leaf blades. Tillering stops when<br />
nitrogen content in the blade becomes 2.0%, phosphorus 0.03%, and potassium<br />
0.5%.<br />
The tillering rate increases linearly with an increasing nitrogen content <strong>of</strong> up to<br />
5%. With phosphorus, the tillering rate increases up to about 0.2%, above which<br />
an increase in phosphorus has no effect on tillering. Similarly, potassium content<br />
as high as 1.5% increases the tillering rate.<br />
The critical phosphorus concentration for tillering appears to be affected by<br />
temperature. Tiller number per square meter increases with an increasing phosphorus<br />
content <strong>of</strong> up to 0.35% in rice crops grown in Hokkaido, Japan, where low<br />
temperatures prevail (Shiga et al 1976). Such a high phosphorus requirement can<br />
be a reason why phosphate applications are particularly beneficial in cool years in<br />
Hokkaido.<br />
An examination <strong>of</strong> tillering is one useful way to examine the growth status <strong>of</strong> a<br />
rice crop. When tillering is retarded by a nutrient shortage, growth parameters<br />
such as leaf area and dry weight also decrease (Table 3.13). The table also<br />
illustrates that any nutrient whose content is below optimum level limits overall<br />
growth even though other nutrients are present in sufficient quantities.<br />
3.6 MINERAL NUTRITION AND PHOTOSYNTHESIS<br />
Nutrient content is related to the photosynthetic activity <strong>of</strong> leaves because essential<br />
nutrients are directly or indirectly involved in photosynthesis and respiration. For<br />
example, nitrogen is a constituent <strong>of</strong> proteins which, in turn, are constituents <strong>of</strong><br />
protoplasm, chloroplasts, and enzymes. Phosphorus as inorganic phosphate, an<br />
energy-rich phosphate compound, and a coenzyme, is directly involved in photosynthesis.<br />
Potassium is involved in opening and closing the stomata that control<br />
carbon dioxide diffusion into green tissues, a first step in photosynthesis (Fujino<br />
1967, Fischer and Hsiao 1968). Potassium is also essential in activating enzymes<br />
such as starch synthetase (Nitsos and Evans 1969).<br />
The relative photosynthetic rate <strong>of</strong> leaf blades is positively correlated with their<br />
nutrient content (Fig. 3.9). The critical nutrient contents for a high leaf photo-