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The development of inflorescences and flowers of three species of Ranunculus and three allied genera ( Ceratocephala, Halerpestes, and Oxygraphis) (Ranunculeae, Ranunculaceae) was studied comparatively using scanning electron microscopy (SEM). Our results showed that both the inflorescence branching patterns and the floral morphogenesis in Ranunculeae are extremely labile. Inflorescences range from a thyrsoid to a solitary flower, with intermediate branching patterns in which sometimes only the terminal flower of the inflorescence main axis fully develops, such as in Ceratocephala and Halerpestes. Only in Oxygraphis is the flower truly solitary. In all species, sepal primordia are broad, crescent-shaped, and truncate, and the primordia of petals, stamens, and carpels are rather small and hemispherical, and very similar to each other. The plastochron between the last sepal and the first petal is relatively long. At the onset of androecium or gynoecium development, the regular spiral pattern of the perianth may become irregular in Ceratocephala and Oxygraphis, whereas spiral and whorled patterns may co-occur in Ranunculus and Halerpestes. The development of the petals is delayed with regard to that of the other floral organs in all species studied here, except for Oxygraphis. Our study confirms that, for solitary flowers, increased number of petals and the shape of the ventral nectary may have evolved independently many times, as suggested by earlier molecular phylogenetic studies and ancestral character reconstructions. With respect to the remainder of the tribe, Oxygraphis displays several autapomorphies, such as nondelayed development and increased number of petals, which will be of interest for comparative molecular developmental studies. [ABSTRACT FROM AUTHOR]

We examined the floral development of Dichocarpum fargesii, Thalictrum fargesii, Thalictrum przewalskii, and Aquilegia yabeana in Thalictroideae, Ranunculaceae, by scanning electron microscope. The sepals are initiated spirally in D. fargesii and A. yabeana, and in two pairs (with four sepals) or spirally (with five sepals) in T. fargesii and T. przewalskii. The petals in D. fargesii and A. yabeana and the stamens and carpels are initiated in a whorled pattern in all three genera. The floral phyllotaxis is whorled in these genera. The primordia of sepals are lunular and truncate, but that of petals and/or stamens are hemispherical, rounded, and much smaller than the sepal primordia. A relatively long plastochron exists between the last sepal and the first petal in D. fargesii and A. yabeana or the first stamen in T. fargesii and T. przewalskii. The similarity between the primordia of petals and stamens may indicate an evolutionary relationship between petals and stamens. The petals develop slower than the stamens in D. fargesii, but faster than stamens in A. yabeana. The early developmental stages of the staminodes in A. yabeana are similar to that of stamens, so they may be phylogenetically homologous organs. The carpel primordia are initiated in a single whorl; are lunular in shape and plicate in A. yabeana and D. fargesii; and are initiated spirally and hemispheric in shape and ascidiate in T. fargesii and T. przewlaskii. The stigma is everted and decurrent with unicellular papillae in T. fargesii and T. przewalskii; the head has unicellular papillae in D. fargesii and is smooth in A. yabeana. The floral development features of Aquilegia are unique in Thalictroideae. [ABSTRACT FROM AUTHOR]