[Correlations between gynoecium morphology and ovary position in angiosperm flowers: roles of developmental and terminological constraints].

Pub Date : 2015-03-01
D D Sokoloff
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Abstract

Angiosperm gynoecium consists of elementary units, called carpels. These can be free (apocarpy) or united (coenocarpy, or syncarpy in a wide sense). One of the most complicate problems of evolutionary morphology of angiosperms is distinguishing monomerous and pseudomonomerous gynoecia. The former are assumed to be derived by reduction of carpel number in apocarpous gynoecia, the latter by reduction of gynoecia with united carpels. Pseudomonomerous gynoecia have one fertile carpel and more or less prominent traces of sterile carpel(s). In extreme cases of reduction, pseudomonomerous gynoecia are very similar to monomerous, even though the two types have completely different evolutionary histories. G.B. Kedrov (1969) proposed a new approach to resolving the issue. Using the fact of absence of polymerous free-carpellate gynoecia with inferior ovaries, he suggested that there is a constraint against epigyny in plants with free carpels. Therefore, in taxa with disputable morphological interpretations, the gynoecium should be treated as pseudomonomerous (and not monomerous) if the ovary is inferior. A critical review of the concept of G.B. Kedrov showed that his ideas would suggest re-interpretation of widely accepted views on gynoecium morphology in several key families of basal angiosperms. An alternative view is proposed, that for most important types of epigyny in angiosperms, a "constraint" for a combination of inferior ovary and apocarpy is due to definition of the term "apocarpy" only. There is no biological sense in this "constraint". Existence of two other morphogenetic constraints is proposed: (1) against development of a typical inferior ovary in monomerous gynoecia with conduplicate carpel and (2) against a radial (sectorial) fusion of individual carpels with stamens or perianth members without fusion of these groups into an entire structure. Possible biological nature of these constraints is discussed.

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被子植物花中雌蕊形态与子房位置的相关性:发育和术语限制的作用。
被子植物雌蕊由称为心皮的基本单位组成。它们可以是自由的(虚构的),也可以是联合的(共同的),或者广义上的syncarpy。被子植物进化形态学中最复杂的问题之一是区分单株和假单株雌蕊。前者被认为是由离生雌蕊的心皮数减少而得出的,后者是由心皮统一的雌蕊数减少而得出的。假单雌雌蕊有一个可育心皮和或多或少明显的不育心皮痕迹。在减少的极端情况下,假单雌体与单雌体非常相似,尽管这两种类型具有完全不同的进化历史。G.B. Kedrov(1969)提出了解决这一问题的新方法。利用下子房不存在聚合无心皮雌蕊的事实,他认为在有游离心皮的植物中存在对附着蕊的限制。因此,在形态学解释有争议的分类群中,如果子房较低,雌蕊应被视为假单体(而不是单体)。对G.B. Kedrov概念的批判性回顾表明,他的观点可能会重新解释被广泛接受的关于基生被子植物几个关键科的雌蕊形态的观点。另一种观点认为,对于被子植物中最重要的附着体类型,下子房和旁室结合的“限制”仅仅是由于术语“旁室”的定义。这种“约束”没有生物学意义。存在另外两种形态发生限制:(1)在单雌心蕊中发育典型的下位子房,具有共重的心皮;(2)单个心皮与雄蕊或花被成员呈放射状(扇形)融合,而这些群体没有融合成一个完整的结构。讨论了这些约束的可能的生物学性质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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