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Ontogenetic changes in the scaling of cellular respiration with respect to size among sunflower seedlings

机译:向日葵幼苗中细胞呼吸的尺度相对于大小的个体发育变化

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摘要

The respiration rates R (oxygen uptake per min) and body mass M (mg per individual) of sunflower (Helianthus annuus L.) seedlings were measured for populations raised in the dark (scotomorphogenesis) and for plants subsequently grown in white light (photomorphogenesis) to determine the allometric (scaling) relationship for R vs. M. Based on ordinary least squares and reduced major axis regression protocols, cellular respiration rates were found to increase non-linearly as a ‘broken-stick’ curve of increasing M. During germination, the scaling was ca. 7.5-fold higher than after the emergence of the cotyledons from the seed coat, which can be attributed to the hypoxic conditions of the enclosed embryo. During seedling development, R was found to scale roughly as the 3/7 power of body mass (i.e., R ∼ M−3/7), regardless of whether plants were grown in the dark or subsequently in white light. The numerical value of 3/7 statistically significantly differs from that reported across small field- or laboratory-grown plants (i.e., R ∼ M−1.0). It also differs from the expectations of recent allometric theory (i.e., R ∼ M−0.75 to M−1.0). This difference is interpreted to be the result of species-specific tissue-compositions that affect the volume fractions of metabolically active and less active cells. These findings, which are supported by cytological and ultrastructural observations (i.e., scanning- and transmission electron micrographs), draw attention to the need to measure R of developing plants in a tissue- or organ-specific context.
机译:测量了在黑暗中生长的种群(scotomorphogenesis)和随后在白光下生长的植物(光形态发生)的向日葵(Helianthus annuus L.)幼苗的呼吸速率R(每分钟吸氧量)和体重M(每人毫克)。以确定R与M的异速关系(缩放)。基于普通最小二乘和减小的主轴回归协议,发现细胞呼吸速率随着M的“折断”曲线非线性增加。 ,缩放比例约为。比从种皮中出现子叶后高7.5倍,这可以归因于封闭胚胎的低氧条件。在幼苗发育过程中,无论植物是在黑暗中生长还是随后在黑暗中生长,都发现R的大小大致是其3/7体重的幂(即R〜M −3/7 )。白光。 3/7的数值在统计上与在田间或实验室种植的小型植物中报告的数值显着不同(即R〜M -1.0 )。它也不同于最近的变构理论的期望(即,R〜M -0.75 到M -1.0 )。该差异被解释为是物种特异性组织组成的结果,该组织组成影响代谢活性和活性较低的细胞的体积分数。这些发现得到细胞学和超微结构观察(即扫描和透射电子显微照片)的支持,使人们注意到对在组织或器官特异性背景下测量发育中植物的R的需要。

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