Goldstein G, Sharifi M R, Kohorn L U, Lighton J R B, Shultz L, Rundel P W
Laboratory of Biomedical and Environmental Sciences, University of California, 900 Veteran Ave., 90024, Los Angeles, CA, USA.
Oecologia. 1991 Jan;85(3):396-402. doi: 10.1007/BF00320616.
The photosynthetic capacity and carbon metabolism of the fruits of Isomeris arborea (Capparidaceae), an evergreen shrub endemic to the desert and coastal habitats of Southern California and Baja California, are described. The inflated structure of the pods of I. arborea provides a model system for experimental studies of fruit photosynthesis in native plants since the gas concentration of the internal space can be manipulated and monitored separately from the external pod environment. CO released by seed respiration is partially contained in the inner gas space of the pods, resulting in an elevated CO environment inside the fruit (500 to 4000 μmol mol depending on the stage of fruit development). A portion of this CO is assimilated by the inner layers of the pericarp, but a larger fraction leaks out. The photosynthetic layers of the pericarp use two different sources of CO: the exocarp fixes exogenous CO while the endocarp fixes CO released by seed respiration into the pod cavity. Even though the total weight of the fruit increases during development, the combined rates of fixation of externally and internally supplied CO remained constant (10-11 μmol CO pod h). After the pods attain maximum volume, the major change in gas exchange that takes place during fruit growth is a gradual increase in the amount of respiratory CO released by the seeds. This shifts the CO balance of the fruit from positive, in young fruits, to negative in mature fruits. Pericarp photosynthesis helped support not only the cost of fruit maintenance, but also the cost of fruit growth, particularly during the first stages of fruit development. During later fruiting stages insufficient carbon is fixed to fully supply either respiration or growth.
描述了南加州和下加利福尼亚沙漠及沿海栖息地特有的常绿灌木乔木异叶木(Capparidaceae)果实的光合能力和碳代谢。乔木异叶木豆荚的膨胀结构为本地植物果实光合作用的实验研究提供了一个模型系统,因为内部空间的气体浓度可以与豆荚外部环境分开进行控制和监测。种子呼吸释放的二氧化碳部分包含在豆荚的内部气体空间中,导致果实内部的二氧化碳环境升高(根据果实发育阶段,为500至4000μmol mol)。其中一部分二氧化碳被果皮内层同化,但较大一部分会泄漏出去。果皮的光合层利用两种不同的二氧化碳来源:外果皮固定外源二氧化碳,而内果皮将种子呼吸释放到豆荚腔中的二氧化碳固定下来。尽管果实重量在发育过程中增加,但外部和内部供应的二氧化碳的固定总速率保持恒定(10 - 11μmol CO 豆荚 h)。在豆荚达到最大体积后,果实生长过程中气体交换的主要变化是种子释放的呼吸二氧化碳量逐渐增加。这使得果实的二氧化碳平衡从幼果期的正值转变为成熟期的负值。果皮光合作用不仅有助于维持果实的成本,还有助于果实生长的成本,特别是在果实发育的最初阶段。在后期结果阶段,固定的碳不足以完全满足呼吸或生长的需求。