Department of Life Sciences, National Chung Hsing University, 250, Kuo Kuang Rd, Taichung 402, Taiwan.
Ann Bot. 2012 May;109(6):1065-74. doi: 10.1093/aob/mcs025. Epub 2012 Feb 23.
Foliar variegation is recognized as arising from two major mechanisms: leaf structure and pigment-related variegation. Begonia has species with a variety of natural foliar variegation patterns, providing diverse examples of this phenomenon. The aims of this work are to elucidate the mechanisms underlying different foliar variegation patterns in Begonia and to determine their physiological consequences.
Six species and one cultivar of Begonia were investigated. Light and electron microscopy revealed the leaf structure and ultrastructure of chloroplasts in green and light areas of variegated leaves. Maximum quantum yields of photosystem II were measured by chlorophyll fluorescence. Comparison with a cultivar of Ficus revealed key features distinguishing variegation mechanisms.
Intercellular space above the chlorenchyma is the mechanism of variegation in these Begonia. This intercellular space can be located (a) below the adaxial epidermis or (b) below the adaxial water storage tissue (the first report for any taxa), creating light areas on a leaf. In addition, chlorenchyma cell shape and chloroplast distribution within chlorenchyma cells differ between light and green areas. Chloroplasts from both areas showed dense stacking of grana and stroma thylakoid membranes. The maximum quantum yield did not differ significantly between these areas, suggesting minimal loss of function with variegation. However, the absence of chloroplasts in light areas of leaves in the Ficus cultivar led to an extremely low quantum yield.
Variegation in these Begonia is structural, where light areas are created by internal reflection between air spaces and cells in a leaf. Two forms of air space structural variegation occur, distinguished by the location of the air spaces. Both forms may have a common origin in development where dermal tissue becomes loosely connected to mesophyll. Photosynthetic functioning is retained in light areas, and these areas do not include primary veins, potentially limiting the costs of variegation.
叶斑是由两种主要机制引起的:叶片结构和与色素有关的叶斑。秋海棠属植物具有多种天然叶斑图案,为这一现象提供了多种示例。本工作的目的是阐明秋海棠不同叶斑图案的形成机制,并确定其生理后果。
研究了秋海棠属的 6 个种和 1 个品种。光镜和电镜揭示了绿色和斑驳叶片浅色区叶结构和叶绿体超微结构。通过叶绿素荧光测量最大光化学量子产量。与榕属品种的比较揭示了区分叶斑机制的关键特征。
叶肉上方的细胞间隙是这些秋海棠属叶斑的形成机制。这个细胞间隙可以位于(a)上表皮下方或(b)上表皮下的水储存组织下方(这是任何分类群的首次报道),在叶片上形成浅色区。此外,浅色区和绿色区的叶肉细胞形状和叶绿体在叶肉细胞内的分布不同。来自这两个区域的叶绿体都显示出类囊体垛叠和基质类囊体膜的密集堆积。这些区域的最大量子产量没有显著差异,表明叶斑形成时功能损失最小。然而,榕属品种叶片浅色区缺乏叶绿体导致量子产量极低。
这些秋海棠属植物的叶斑是结构性的,通过叶片内空气间隙和细胞之间的内部反射形成浅色区。两种形式的空气空间结构叶斑通过空气间隙的位置来区分。这两种形式可能在发育过程中有共同的起源,其中表皮组织与叶肉组织变得松散连接。浅色区保留了光合作用功能,且这些区域不包括主叶脉,可能限制了叶斑形成的成本。