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Postanthesis Nitrate Assimilation in Winter Wheat 1: In Situ Flag Leaf Reduction

机译:冬小麦花后硝酸盐吸收同化1:原位旗叶减少

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摘要

When adequate levels of soil NO3− are available, concurrent NO3− absorption and assimilation, and mobilization of vegetative N reserves accumulated prior to anthesis, may be used to supply N to developing wheat (Triticum aestivum L.) kernels. Vegetative wheat components (stems, leaves, spike) are known to possess NO3− reductase activity, but the in situ utilization of NO3− translocated to the shoot has not been studied. Assimilation and partitioning of 15N was determined in winter wheat `Doublecrop.' At 7 days after anthesis, the stem immediately above the peduncle node was heat girdled to block phloem export from the flag leaf. Control plants were not girdled. One day later, 50 micromoles of 15NO3− (98 atom percent 15N) was injected into the penultimate internodal lacuna, after which 15NO3− utilization was determined sequentially over a 5 day period. Based on differences in spike accumulation of reduced 15N excess between treatments and the amount of reduced 15N excess remaining in the flag leaf, it was estimated that the flag leaf contributed 37% of the total reduced 15N excess in the injected shoot. The lower shoot contribution was 18% and that of the peduncle plus spike was 45%.
机译:当有足够水平的土壤NO3-可用时,同时使用NO3-吸收和同化以及动植物前积累的植物性N储备可用于向发育中的小麦(Triticum aestivum L.)籽粒供应N。已知营养小麦成分(茎,叶,穗)具有NO3-还原酶活性,但尚未研究将NO3-转移到芽上的原位利用。在冬小麦“ Doublecrop”中确定了15N的吸收和分配。花后7天,对刚好位于花梗节上方的茎进行热喷磨处理,以阻止韧皮部从旗叶中导出。对照植物没有环带。一天后,将50微摩尔的15NO3-(98%原子百分比的15N)注入倒数第二个节间空隙,然后在5天的时间内顺序确定15NO3-的利用率。根据处理之间减少的15N过量的穗累积的累积差异和旗叶中剩余的减少的15N过量的数量的差异,估计在注射的新梢中,旗叶贡献了减少的15N过量总量的37%。较低的嫩芽贡献率为18%,而花梗加穗的嫩芽贡献率为45%。

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