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Physiological, biochemical, and fluorescence parameters of senescing sugar beet leaves in the vegetative phase of growth

机译:营养生长阶段甜菜叶片衰老的生理,生化和荧光参数

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The phase of vegetative growth of sugar beet (Beta vulgaris L., single-sprout form) was conditionally subdivided into four periods according to leaf number and size (including already withered leaves): (A) 8 pl 1 weeks after seedling emergence (wase) (5-7 leaves); (B) 11 pl 1 wase (10-12 leaves); (C) 14 wase (13-15 leaves); (D) 15 wase (15-18 leaves). It took each next leaf about 1 week to come into view. In the course of leaf senescence, palisade parenchyma became less ordered; cells, vacuoles, and intercellular spaces expanded; leaf area and thickness increased. Chloroplasts became swollen, starch grains (and later osmiophilic globules) accumulated and degraded. In every growth period, the highest levels of soluble carbohydrates (sCH), chlorophyll (Chl (a + b)), soluble protein, and the highest activities of rubisco and soluble carboanhydrase usually preceded the full leaf expansion. In unfolded leaves at the growth period B, the maximum values of biochemical characteristics were as a rule higher than at the growth periods A and C and especially D. The only exception was Chl (a + b) with its peak level somewhat increased with plant age. Occurrence of peak values of individual characteristics depended on plant growth period. These characteristics started diminishing asynchronously, with a minimum in old operational leaves. Only the sCH content in the leaves at the periods C and D was stable. Changes in quantum yield at PSII and nonphotochemical fluorescence quenching reflected the age-associated differences in biochemical characteristics. The results are discussed in the light of the idea that leaf senescence is a normal stage of development directly related to the changes in source-sink relations. Biochemically, this stage comprises the degradation of temporarily stored products and partial utilization of the breakdown products for maintenance of the growth of newly formed leaves and root.
机译:根据叶的数量和大小(包括已经枯萎的叶子),将甜菜(单子叶形式的Beta)的营养生长阶段有条件地分为四个时期:(A)幼苗出苗后1周(收获)8 pl )(5-7片叶子); (B)11 pl 1麦子(10-12片叶子); (C)14块(13-15片叶子); (D)15块(15-18片叶子)。接下来的每一片叶子花了大约1周的时间才出现。在叶片衰老的过程中,栅栏薄壁组织变得不规则。细胞,液泡和细胞间空间扩大;叶面积和厚度增加。叶绿体变得肿胀,淀粉颗粒(以及后来的同渗性小球)积累并降解。在每个生长期,通常在叶片完全膨胀之前,可溶性碳水化合物(sCH),叶绿素(Chl(a + b)),可溶性蛋白以及活性最高的Rubisco和可溶性碳酸酐酶含量最高。在生长期B的未折叠叶片中,生化特性的最大值通常高于生长期A和C,尤其是生长期D。唯一的例外是Chl(a + b),其峰值水平随植物而有所增加年龄。各个特征的峰值的出现取决于植物的生长期。这些特性开始异步减少,而旧的运行时间最少。在C和D期,只有叶片中的sCH含量稳定。 PSII处量子产率的变化和非光化学荧光猝灭反应反映了与年龄相关的生化特征差异。根据认为叶衰老是发育的正常阶段这一思想进行了讨论,该衰老与源库关系的变化直接相关。生化阶段,此阶段包括暂时存储产品的降解和分解产品的部分利用,以维持新形成的叶和根的生长。

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