Macadam J W, Volenec J J, Nelson C J
Department of Agronomy, University of Missouri, Columbia, Missouri 65211.
Plant Physiol. 1989 Feb;89(2):549-56. doi: 10.1104/pp.89.2.549.
Leaf elongation rate (LER) in grasses is dependent on epidermal cell supply (number) and on rate and duration of epidermal cell elongation. Nitrogen (N) fertilization increases LER. Longitudinal sections from two genotypes of tall fescue (Festuca arundinacea Schreb.), which differ by 50% in LER, were used to quantify the effects of N on the components of epidermal cell elongation and on mesophyll cell division. Rate and duration of epidermal cell elongation were determined by using a relationship between cell length and displacement velocity derived from the continuity equation. Rate of epidermal cell elongation was exponential. Relative rates of epidermal cell elongation increased by 9% with high N, even though high N increased LER by 89%. Duration of cell elongation was approximately 20 h longer in the high- than in the low-LER genotype regardless of N treatment. The percentage of mesophyll cells in division was greater in the high- than in the low-LER genotype. This increased with high N in both genotypes, indicating that LER increased with cell supply. Division of mesophyll cells adjacent to abaxial epidermal cells continued after epidermal cell division stopped, until epidermal cells had elongated to a mean length of 40 micrometers in the high-LER and a mean length of 50 micrometers in the low-LER genotype. The cell cycle length for mesophyll cells was calculated to be 12 to 13 hours. Nitrogen increased mesophyll cell number more than epidermal cell number: in both genotypes, the final number of mesophyll cells adjacent to each abaxial epidermal cell was 10 with low N and 14 with high N. A spatial model is used to describe three cell development processes relevant to leaf growth. It illustrates the overlap of mesophyll cell division and epidermal cell elongation, and the transition from epidermal cell elongation to secondary cell wall deposition.
禾本科植物的叶片伸长率(LER)取决于表皮细胞供应(数量)以及表皮细胞伸长的速率和持续时间。施氮会提高LER。利用两种高羊茅(Festuca arundinacea Schreb.)基因型的纵切片来量化氮对表皮细胞伸长成分和叶肉细胞分裂的影响,这两种基因型的LER相差50%。表皮细胞伸长的速率和持续时间是通过利用从连续性方程推导出来的细胞长度与位移速度之间的关系来确定的。表皮细胞伸长速率呈指数关系。即使高氮使LER提高了89%,高氮条件下表皮细胞伸长的相对速率仍提高了9%。无论氮处理如何,高LER基因型的细胞伸长持续时间比低LER基因型大约长20小时。高LER基因型中处于分裂状态的叶肉细胞百分比高于低LER基因型。在两种基因型中,这一比例都随着高氮处理而增加,表明LER随着细胞供应的增加而提高。在表皮细胞分裂停止后,与远轴表皮细胞相邻的叶肉细胞仍继续分裂,直到高LER基因型中的表皮细胞伸长到平均长度40微米,低LER基因型中的表皮细胞伸长到平均长度50微米。叶肉细胞的细胞周期长度经计算为12至13小时。氮增加的叶肉细胞数量多于表皮细胞数量:在两种基因型中,每个远轴表皮细胞相邻的叶肉细胞最终数量在低氮条件下为10个,在高氮条件下为14个。一个空间模型被用来描述与叶片生长相关的三个细胞发育过程。它说明了叶肉细胞分裂和表皮细胞伸长的重叠,以及从表皮细胞伸长到次生细胞壁沉积的转变。