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首页> 外文期刊>Philosophical Transactions of the Royal Society of London, Series B. Biological Sciences >Defining the limits of flowers: the challenge of distinguishing between the evolutionary products of simple versus compound strobili
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Defining the limits of flowers: the challenge of distinguishing between the evolutionary products of simple versus compound strobili

机译:定义花朵的界限:区分简单与复合可塑性的进化产物的挑战

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Recent phylogenetic reconstructions suggest that axially condensed flower-like structures evolved iteratively in seed plants from either simple or compound strobili. The simple-strobilus model of flower evolution, widely applied to the angiosperm flower, interprets the inflorescence as a compound strobilus. The conifer cone and the gnetalean ‘flower’ are commonly interpreted as having evolved from a compound strobilus by extreme condensation and (at least in the case of male conifer cones) elimination of some structures present in the presumed ancestral compound strobilus. These two hypotheses have profoundly different implications for reconstructing the evolution of developmental genetic mechanisms in seed plants. If different flower-like structures evolved independently, there should intuitively be little commonality of patterning genes. However, reproductive units of some early-divergent angiosperms, including the extant genus Trithuria (Hydatellaceae) and the extinct genus Archaefructus (Archaefructaceae), apparently combine features considered typical of flowers and inflorescences.We re-evaluate several disparate strands of comparative data to explore whether flower-like structures could have arisen by co-option of flower-expressed patterning genes into independently evolved condensed inflorescences, or vice versa. We discuss the evolution of the inflorescence in both gymnosperms and angiosperms, emphasising the roles of heterotopy in dictating gender expression and heterochrony in permitting internodal compression.
机译:最近的系统发育重建表明,轴向浓缩的花状结构在种子植物中从简单或复合可塑性开始迭代地进化。花进化的简单球茎模型被广泛应用于被子植物花,将花序解释为复合球茎。针叶树锥和gnetalean的“花”通常被解释为是由于极端凝结和(至少在雄性针叶树锥的情况下)消除了假定的祖先复合体中存在的某些结构而从复合体中演化而来的。这两个假设对于重构种子植物发育遗传机制的进化具有深远的不同含义。如果不同的花朵状结构独立地进化,则直观地讲,模式基因的共同性应该很小。但是,一些早散的被子植物的生殖单位,包括现存的Trithuria(Hydatellaceae)和已灭绝的Archaefructus(Archaefructaceae)属,显然结合了花和花序的典型特征。我们重新评估了几条不同的比较数据来探索是否可以通过将表达花的图案基因共同选择为独立进化的浓缩花序而出现类似花的结构,反之亦然。我们讨论裸子植物和被子植物花序的演变,强调异位在指示性别表达和异时性在允许节间压迫中的作用。

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