Department of Botany, University of California, Davis, California 95616.
Plant Physiol. 1988 Mar;86(3):782-5. doi: 10.1104/pp.86.3.782.
When leaves of Alocasia macrorrhiza adapted to 10 micromole quanta per square meter per second were transferred to 500 micromole quanta per square meter per second, the rate of photosynthetic CO(2) assimilation increased for over 45 minutes. For the first 10 to 15 minutes, increases in both stomatal conductance and the leaf's photosynthetic capacity were responsible for the increase in assimilation rate. Thereafter, continuing increases in stomatal conductance were almost entirely responsible for further increases in assimilation rate. When conductances were initially high, assimilation rates 1 minute after the increase in photon flux density could be more than six times as high as for similar leaves with initially low conductance. Further increases in assimilation rate in these leaves with high conductance were predominantly due to increases in the induction state at the biochemical level and followed an exponential time course. When stomatal conductances were initially low, then increases in conductance were predominantly responsible for the increases in assimilation rate, with both following a sigmoidal time course. In these leaves, it was important to also consider the effect of cuticular water loss on the calculation of the intracellular partial pressure of CO(2), and an assessment of the relative importance of stomatal conductance differed considerably from one that did not include cuticular water loss.
当适应于每平方米每秒 10 微摩尔量子的 Alocasia macrorrhiza 叶片被转移到每平方米每秒 500 微摩尔量子时,光合作用 CO2 同化的速率增加了超过 45 分钟。在最初的 10 到 15 分钟内,气孔导度和叶片光合作用能力的增加共同导致了同化速率的增加。此后,气孔导度的持续增加几乎完全负责进一步提高同化速率。当导度最初较高时,在光量子通量密度增加 1 分钟后,同化速率可能比初始导度较低的类似叶片高六倍以上。在这些高导度叶片中,同化速率的进一步增加主要归因于生物化学水平上诱导状态的增加,并遵循指数时间过程。当气孔导度最初较低时,导度的增加主要负责提高同化速率,两者都遵循双曲线时间过程。在这些叶片中,还必须考虑表皮水分损失对细胞内 CO2 分压计算的影响,并且不包括表皮水分损失的评估对气孔导度相对重要性的评估有很大的不同。