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Crop yield response to water - Cra

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selected with a tendency <strong>to</strong> set more fruit than can be filled with the available pho<strong>to</strong>syntheticassimilates, leading <strong>to</strong> the abortion of a portion of the set fruit early in their development.So reduction of fruit set by <strong>water</strong> stress may or may not reduce HI, depending on the exten<strong>to</strong>f the reduction and the extent of the excessive fruit setting. Aqua<strong>Crop</strong> simulates this alsowith the Ks approach, <strong>to</strong> reduce pollination (hence fruit set) each day according <strong>to</strong> the exten<strong>to</strong>f <strong>water</strong> depletion. The effect on HI is adjusted for tendency <strong>to</strong> set excess fruit by providingcategories differing in excessiveness.Another negative impact on HI is the underfilling and abortion of younger fruits resultingfrom a lack of pho<strong>to</strong>synthetic assimilates. Pho<strong>to</strong>synthesis is tightly correlated with s<strong>to</strong>matalconductance. Water stress, by reducing s<strong>to</strong>matal opening, diminishes the amount of assimilatesavailable <strong>to</strong> fill all developing fruit. The youngest fruit are then the most likely <strong>to</strong> be abortedand only the older fruit mature, but likely underfilled. This occurs during the grain filling andmaturing period, when most of the vegetative growth has already taken place and most ofthe assimilates go <strong>to</strong> the grain. Aqua<strong>Crop</strong> simulates this in two ways, one is simply by reducingHI with a coefficient that is a function of Ks for s<strong>to</strong>mata. S<strong>to</strong>matal closure may often be onlythe minor cause, however, because <strong>water</strong> stress at this growth stage commonly acceleratescanopy senescence, resulting in an early decline in pho<strong>to</strong>synthetic surface area and shortensthe duration of the canopy. As programmed in Aqua<strong>Crop</strong>, HI increases continuously up <strong>to</strong>the time of normal maturity (Figure 6), but only if a portion of the green canopy remains. AsCC declines <strong>to</strong> some low limit value, HI is considered <strong>to</strong> have reached its final value. With CCreaching this low limit earlier because of stress induced early senescence, HI is au<strong>to</strong>maticallyreduced. This effect can be dramatic if canopy duration is shortened substantially.The last of the negative impacts on HI has <strong>to</strong> do with not having sufficient <strong>water</strong> stress. Thiscentres on the competition between vegetative and reproductive growth, which also accountsfor the positive impact of <strong>water</strong> stress on HI. As demonstrated for cot<strong>to</strong>n and some other crops,HI can be reduced by overly luxurious vegetative (leaf) growth during the reproductive phasewhen <strong>water</strong> is fully available, while restricting vegetative growth by mild <strong>water</strong> (and nitrogen)stress is known <strong>to</strong> enhance HI. The cause is apparently the competition for assimilates. Negativeeffect on HI comes about when high <strong>water</strong> availability stimulates fast leaf growth, with <strong>to</strong>omany assimilates diverted <strong>to</strong> the vegetative organs, depriving the younger potential flowers ornascent fruits so they drop off the crop. The end result is that <strong>to</strong>o few fruits mature, reducingHI. On the other hand, mild <strong>water</strong> stress would reduce leaf growth substantially because it ismost sensitive <strong>to</strong> <strong>water</strong> stress, while s<strong>to</strong>mata, being substantially less sensitive, would remainopen <strong>to</strong> maintain pho<strong>to</strong>synthesis. Consequently, without the excessive diversion <strong>to</strong> vegetativeorgans, an ample amount of assimilates are available <strong>to</strong> enhance fruit retention and growth,leading <strong>to</strong> higher HI. Aqua<strong>Crop</strong> simulates this behaviour relying on the Ks functions for leafgrowth (Ks exp,w ) and for s<strong>to</strong>mata closure (Ks s<strong>to</strong> ), with HI being enhanced as Ks exp,w declines,and being reduced as Ks s<strong>to</strong> declines. In the adjustment, HI is first enhanced as stress developsand vegetative growth is inhibited, then is more enhanced as stress intensifies, until s<strong>to</strong>matabegin <strong>to</strong> close restricting pho<strong>to</strong>synthesis, at which point the HI does not change. At some levelof stress severity HI is reduced <strong>to</strong> the normal value because the positive effect of leaf growthinhibition is counterbalanced by the negative effect of s<strong>to</strong>mata closure. As stress intensifiesbeyond this level, the overall effects would switch <strong>to</strong> negative with proper programme settingparameters (Figure 13).36crop <strong>yield</strong> <strong>response</strong> <strong>to</strong> <strong>water</strong>

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