Abstract
Hybridization in flowering plants depends, in the first place, on the delivery of pollen to a receptive stigma and the subsequent growth of pollen tubes through the style to the ovary, where the sperm nucleus of the pollen grain can ultimately fertilize the egg cell. However, reproductive failure is often observed in distant crosses and is caused by pre- and/or post-zygotic barriers. In this study, the reproductive pre-fertilization barriers of intertribal crosses between Anemone coronaria L. and Ranunculus asiaticus L., both belonging to the Ranunculaceae, were investigated. Despite the incongruity of intertribal crosses between A. coronaria and R. asiaticus having been of low intensity at the stigmatic level, interstylar obstructions of the pollen tube growth occurred, which confirmed the presence of pre-fertilization barriers. We show that these barriers could be partially bypassed by combining pollination with a stigma treatment. More specifically, a significantly higher ratio of the pollen tube length to the total style length and a better seed set were observed when the stigma was treated with the auxin 2,4-dichlorophenoxyacetic acid (2,4-D, 1 mg·mL−1) together with the cytokinin kinetin (KIN, 0.5 mg·mL−1) 24 h after pollination, irrespective of the cross direction. More specifically, the stigma treatments with any form of auxin (combined or not combined with cytokinin) resulted in a full seed set, assuming an apomictic fruit set, because no pollination was needed to obtain these seeds.
Highlights
Plant variation is the driving force in ornamental plant cultivation
Using Anemone as a mother plant resulted in higher ratios of the pollen tube length to the total style length compared with the reciprocal crosses, except for R
In the intertribal crosses between A. coronaria and R. asiaticus, the Anemone × Ranunculus cross clearly resulted in higher ratios of pollen tube lengths to total style lengths than had the reciprocal cross
Summary
Plant variation is the driving force in ornamental plant cultivation. Crosses between partners with a high genetic distance are important inducers of variation, provided they produce viable seeds. Often incongruity occurs, which can be defined as a mechanism for the common phenomenon of non-functioning of pollen–pistil relationships in interpopulational matings [1] This is not the same as incompatibility, which is based on a non-recognition system between a male and female determinant (S-locus) [2]. These interpopulational reproductive barriers occur in and can be divided into pre-zygotic (or pre-fertilization) and post-zygotic (or post-fertilization) barriers, depending on the time and place of occurrence [3,4,5,6,7]. Stigmas are divided in dry and wet stigmas depending on the occurrence
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