水分亏缺对珍珠粟对氮的响应

Agronomie Pub Date : 2004-03-01 DOI:10.1051/AGRO:2004001
O. Diouf, Y. C. Brou, Mayécor M. Diouf, B. Sarr, M. Eyletters, H. Roy-Macauley, J. Delhaye
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引用次数: 25

摘要

在萨赫勒地区,土壤氮含量低可能与干旱一样限制珍珠粟的生产。尽管谷子的生长和产量依赖于几种生化反应,其中氮代谢起着重要作用,但氮水互作对谷子氮吸收和关键酶硝还原酶和谷氨酰胺合成酶的影响尚不清楚。为此,谷子品种cv。旱季采用分畦试验设计,在3个氮肥水平(NO = 0.0, N1 = 17.13, N2 = 68.50 kg N ha -1)和不同水分状况(丰水和缺水)的条件下进行田间种植。在分蘖、籽粒形成和灌浆阶段,对缺水植物停止灌溉,从而产生两个亏水循环。各施氮处理在开花前吸收了大量的调动态氮(79% ~ 100%)。氮素吸收量仅在第二次亏水循环中显著下降。在第一个水分亏缺循环中,地上生物量减少,维持氮素吸收导致氮和硝酸盐浓度增加。水分亏缺降低了所有处理的硝酸还原酶活性,在高氮条件下效果更大。水分亏缺条件下硝酸盐浓度的增加表明硝酸还原酶活性的降低可能不是由于限制硝酸盐。低氮、N1和N0处理下谷氨酰胺合成酶活性较高,说明硝态氮和铵态氮对谷氨酰胺合成酶活性没有刺激作用。根据这些结果对籽粒氮和籽粒产量的影响进行了讨论。
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Response of Pearl Millet to nitrogen as affected by water deficit
In the Sahelian zone, low soil N could be as limiting as drought in pearl millet production. Although growth and crop productivity depend on several biochemical reactions in which the nitrogen metabolism plays a great role, there is little information available on how N uptake and key enzymes, nitrate reductase and glutamine synthetase, are affected by nitrogen and water interaction in millet. For this purpose, the millet variety cv. Souna III was grown in the field during the dry season under three levels of nitrogen fertilization (NO = 0.0, N1 = 17.13, and N2 = 68.50 kg N ha -1 ) and different water regimes (well-watered and water-stressed) in a split-plot experimental design. Irrigation was stopped for water-stressed plants during tillering, and the grain formation and filling phases, thereby giving rise to two water deficit cycles. A major quantity of mobilized N (79-100%) was taken up before flowering in all N treatments. Nitrogen uptake declined significantly only during the second water deficit cycle. During the first water deficit cycle, aboveground biomass was reduced and the maintenance of the N uptake resulted in increased N and nitrate concentrations. The water deficit reduced nitrate reductase activity in all treatments and the effect was greater under high N. The increase in nitrate concentration under water deficit conditions showed that the reduction in nitrate reductase activity was probably not due to limiting nitrates. Glutamine synthetase activity was higher under the low N treatments, N1 and N0, showing the absence of a stimulating effect of glutamine synthetase activity by nitrate or ammonium. These results are discussed on the basis of their effect on grain N and grain yield.
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