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RA 00110.pdf - OAR@ICRISAT

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The conservative nature of qD is extremely valuable<br />

for modeling productivity in dry areas.<br />

Synthesis<br />

Whereas temperature and solar radiation set the<br />

upper limit for productivity of a given cultivar in wet<br />

climates, extractable water and saturation deficit set<br />

this limit in dry environments. Relations have been<br />

calculated between W and D for pearl millet at two<br />

extreme values of extractable water corresponding<br />

to the range defined by Russell (1978) for soils at<br />

Hyderabad (Fig. 6). The total mass of pearl millet in<br />

postrainy seasons is unlikely to rise above 10 t ha -1<br />

and will generally be much smaller.<br />

Table 3 . M a i n factors d e t e r m i n i n g f i n a l standing d r y<br />

weight.<br />

(a) S o i l water n o t l i m i t i n g<br />

Stand<br />

I I<br />

I I I<br />

(b) S o i l water l i m i t i n g<br />

Stand<br />

I V<br />

V<br />

0.50<br />

0.42<br />

W<br />

0.22<br />

0.12<br />

P<br />

0.83<br />

0.80<br />

E 4<br />

0.31<br />

0.36<br />

e 3<br />

0.61<br />

0.56<br />

0.60<br />

0.35<br />

1. W = dry matter production.<br />

2. f = fraction of mean daily insolation intercepted by the canopy.<br />

3. e = amount of dry matter formed per unit radiation intercepted<br />

(conversion coefficient).<br />

4. E = amount of water that the crop extracts from the soil.<br />

5. D = saturation vapor pressure deficit.<br />

Limitations to<br />

Productivity—Summary<br />

Productivity and its causative factors, for the stands<br />

in Table 1, are expressed as a fraction of stand I, the<br />

most productive (Table 3). For the two stands for<br />

which water was not limiting, W was reduced mainly<br />

through effects on the conversion coefficient (e);<br />

mean fractional interception was reduced by only<br />

20%, a consequence of unknown factors mainly<br />

20<br />

affecting maximum leaf area. The reduction in e<br />

(0.61) for stand I I , which grew in a similar atmospheric<br />

environment to stand I, was entirely related to<br />

senescence after anthesis. This effect was by far the<br />

largest limiting productivity in moist conditions.<br />

The additional reduction in e (0.56) for stand I I I may<br />

have been caused by the effect of D on photosynthesis<br />

referred to earlier.<br />

For the two stands, IV and V, for which water was<br />

limiting, W was reduced through effects both of<br />

extracted water (E) and of D operating via qD. In<br />

the extreme case of stand V for which productivity<br />

was reduced by a factor of about 8, both E and q in<br />

Equation 3 were reduced by factors of about 2.8. The<br />

difference in W (a factor of almost 2) between stands<br />

IV and V growing in very different environments but<br />

extracting a similar amount of water was predominantly<br />

caused by a difference in D.<br />

10<br />

200 mm<br />

95 mm<br />

0<br />

0 2.0 4.0<br />

S a t u r a t i o n d e f i c i t (kPa)<br />

Figure 6. Modeled relation between final dry mass of<br />

pearl millet and saturation deficit for representative<br />

soils. Numbers by curves show volumes of extractable<br />

water in the top 1.5 m of soil.<br />

Partition of Assimilate<br />

In wet climates, the amount of dry matter allocated<br />

to the organs that constitute yield can be considered<br />

in terms of the factors in Equation 1, with the addition<br />

of a fraction (p) defined as the fraction of total<br />

dry matter ( T D M ) allocated to the relevant organ.<br />

As the process of allocation usually coincides with<br />

an associated developmental phase, its duration is<br />

strongly governed by temperature above a base and<br />

can be defined as a thermal duration (Ong 1983b,<br />

1984; G.R. Squire, personal communication). In<br />

controlled environments at Nottingham, the partition<br />

fraction changed little (about 0.4) over the<br />

226

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