Sokoloff D D
Zh Obshch Biol. 2015 Mar-Apr;76(2):146-60.
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.
被子植物的雌蕊群由基本单位心皮组成。心皮可以是离生的(离生心皮雌蕊群)或合生的(合生心皮雌蕊群,广义上也称为合心皮雌蕊群)。被子植物进化形态学中最复杂的问题之一是区分单雌蕊和假单雌蕊。前者被认为是由离生心皮雌蕊群中心皮数量减少衍生而来,后者是由合生心皮雌蕊群减少而来。假单雌蕊有一个可育心皮和或多或少明显的不育心皮痕迹。在极端简化的情况下,假单雌蕊与单雌蕊非常相似,尽管这两种类型有着完全不同的进化历史。G.B. 凯德罗夫(1969年)提出了一种解决该问题的新方法。基于不存在具下位子房的多心皮离生心皮雌蕊群这一事实,他认为对于具离生心皮的植物,存在一种阻止子房上位的限制因素。因此,在形态解释存在争议的分类群中,如果子房是下位的,雌蕊群应被视为假单雌蕊(而非单雌蕊)。对G.B. 凯德罗夫概念的批判性审视表明,他的观点将意味着重新解释基部被子植物几个关键科中关于雌蕊群形态的广泛接受的观点。本文提出了另一种观点,即对于被子植物中最重要的子房上位类型,子房下位与离生心皮组合的“限制因素”仅仅是由于“离生心皮”这一术语的定义。这种“限制因素”没有生物学意义。本文提出了另外两种形态发生限制因素:(1)阻止具对折心皮的单雌蕊中典型下位子房的发育;(2)阻止单个心皮与雄蕊或花被片进行辐射状(扇形)融合而这些组不融合成一个整体结构。本文讨论了这些限制因素可能的生物学本质。