Anderson Gregory J, Symon David E
Department of Ecology and Evolutionary Biology U-43, The University of Connecticut, Storrs, CT, 06268.
The State Herbarium of South Australia, North Terrace, Adelaide, South Australia, 5000, AUSTRALIA.
Evolution. 1989 Jan;43(1):204-219. doi: 10.1111/j.1558-5646.1989.tb04218.x.
Field and laboratory studies of 19 diclinous species endemic to Australia help to clarify the nature and evolution of andromonoecy, androdioecy, and dioecy in the genus Solanum. Ten species are andromonoecious; typically these species bear inflorescences with a single, large basal hermaphroditic flower and 12-60 distal, smaller staminate flowers. We suggest that the andromonoecious condition was derived from hermaphroditic-flowered ancestors in part by hemisterilization of flowers but largely by addition of staminate flowers. The resultant larger inflorescences are hypothesized to serve both to attract and to entrain pollinators, yielding more or higher-quality seed set in hermaphroditic flowers and/or greater dispersion of pollen from staminate flowers. We suggest that andromonoecy may also serve to reduce selling. Nine other species are morphologically androdioecious but functionally dioecious. In these species, staminate flowers, like those of the andromonoecious species, bear anthers with copious tricolporate pollen and a highly reduced gynoecium. The morphologically hermaphroditic flowers are functionally pistillate and borne singly in inflorescences, and they bear anthers with inaperturate pollen. The inaperturate pollen, although viable, never germinates and is hypothesized to be retained in pistillate flowers as a reward to pollinators in the nectarless Solanum flowers. All other species of Solanum studied with pollen dimorphism in which one pollen morph is inaperturate are also best treated as functionally dioecious. We conclude that there is no evidence for androdioecy in Solanum. A review of other families suggests that there is little support for this unusual breeding system in any other angiosperm group either. Preliminary analyses suggest that andromonoecy and dioecy are polyphyletic in Solanum. Furthermore, dioecy is as likely to have arisen from hermaphroditic as from andromonoecious ancestors.
对澳大利亚特有的19种雌雄异花植物进行的野外和实验室研究,有助于阐明茄属植物中雄花两性花同株、雄花两性花异株和雌雄异株的本质及进化过程。有10个物种是雄花两性花同株的;通常这些物种的花序带有一朵单生的、位于基部的大型两性花以及12 - 60朵位于远端的、较小的雄花。我们认为,雄花两性花同株的情况部分是由两性花的半不育产生的,但主要是通过添加雄花从两性花的祖先演化而来。据推测,由此产生的较大花序既能吸引传粉者,又能引导传粉者,从而使两性花产生更多或更高质量的种子,和/或使雄花的花粉得到更广泛的传播。我们认为雄花两性花同株也可能有助于减少自交。另外9个物种在形态上是雄花两性花异株,但功能上是雌雄异株。在这些物种中,雄花与雄花两性花同株的物种一样,花药带有大量三沟孔花粉且雌蕊高度退化。形态上为两性花的花朵在功能上是雌蕊花,单生于花序中,其花药带有无萌发孔的花粉。这种无萌发孔的花粉虽然有活力,但从不萌发,据推测它保留在雌蕊花中,作为对无花蜜的茄属花朵传粉者的一种回报。所有其他研究过的具有花粉二态性(其中一种花粉形态无萌发孔)的茄属物种在功能上也最好被视为雌雄异株。我们得出结论,茄属中没有雄花两性花异株的证据。对其他科的综述表明,在任何其他被子植物类群中,对这种不寻常的繁殖系统也几乎没有支持。初步分析表明,雄花两性花同株和雌雄异株在茄属中是多系的。此外,雌雄异株从两性花祖先演化而来的可能性与从雄花两性花同株祖先演化而来的可能性一样大。