Endress P K
Institute of Systematic Botany, University of Zurich, Zollikerstrasse 107, 8008 Zurich, Switzerland.
J Exp Zool. 2001 Aug 15;291(2):105-15. doi: 10.1002/jez.1063.
Flowers evolved in many steps, probably starting long before flowering plants (angiophytes) originated. Certain parts of flowers are conservative and have not changed much during evolution; others are evolutionarily highly plastic. Here conservative features are discussed and an attempt is made to trace them back through their evolutionary history. Microsporangia and ovules (which develop into seeds) are preangiophyte floral elements. Angiospermy, combined with postgenital fusion, was the most prominent key innovation in angiophytes. Angiospermy and thecal organization of stamens originated earlier than all clades of extant angiosperms (the crown group of angiophytes). Differentiation of a perianth into calyx and corolla and syncarpy appeared after the first branching of the basalmost clades of extant angiosperms. Sympetaly and floral tubes as well as tenuinucellar, unitegmic ovules originated as major innovations in the clade that led to asterids. An obvious trend in flower evolution is increased synorganisation of parts, which led to new structures. Fixation of floral organ number and position was a precondition for synorganization. Concomitantly, plasticity changed from number and position of organs to shape of the new structures. Character distribution mapped onto cladograms indicates that key innovations do not appear suddenly, but start with trials and only later become deeply rooted genetically in the organization. This is implied from the common occurrence of reversals in the early history of an innovation. J. Exp. Zool. (Mol. Dev. Evol.) 291:105-115, 2001.
花的进化经历了许多阶段,可能早在开花植物(被子植物)起源之前就开始了。花的某些部分较为保守,在进化过程中变化不大;而其他部分则具有高度的进化可塑性。本文将讨论花的保守特征,并尝试追溯其进化历史。小孢子囊和胚珠(发育成种子)是被子植物出现之前的花部结构。被子植物状态与后生融合相结合,是被子植物中最显著的关键创新。被子植物状态和雄蕊的花药结构起源早于所有现存被子植物类群(被子植物的冠群)。花被分化为花萼和花冠以及合心皮现象出现在现存被子植物最基部类群的首次分支之后。花瓣联合和花管以及薄珠心、单珠被胚珠是在导致菊类植物的分支中作为主要创新出现的。花进化的一个明显趋势是各部分的协同组织增加,这导致了新结构的出现。花器官数量和位置的固定是协同组织的前提条件。与此同时,可塑性从器官的数量和位置转变为新结构的形状。将特征分布映射到系统发育树上表明,关键创新并非突然出现,而是始于尝试,之后才在组织中通过基因深深扎根。这一点从创新早期历史中常见的逆转现象可以推断出来。《实验动物学杂志(分子发育与进化)》291:105 - 115,2001年。