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Unfertilized ovary pushes wheat flower open for cross-pollination.

ABSTRACT: Bread wheat is strongly autogamous; however, an opportunity for outcrossing occurs when self-pollination fails and florets open. The first phase of floret opening at anthesis is short and induced by lodicule turgidity. Some wheat florets re-open post-anthesis for several days, known as the 'second opening', for which the underlying mechanisms are largely unknown. We performed detailed physiological, anatomical, and histological investigations to understand the biological basis of the flower opening process. Wheat florets were observed open when the ovary was unfertilized. Unfertilized ovaries significantly increased in radial size post-anthesis, pushing the lemma and palea apart to open the florets. The absence of fertile pollen was not directly linked to this, but anther filament elongation coincided with initiation of ovary swelling. The pericarp of unfertilized ovaries did not undergo degeneration as normally seen in developing grains, instead pericarp cells remained intact and enlarged, leading to increased ovary radial size. This is a novel role for the ovary pericarp in wheat flower opening, and the knowledge is useful for facilitating cross-pollination in hybrid breeding. Ovary swelling may represent a survival mechanism in autogamous cereals such as wheat and barley, ensuring seed set in the absence of self-fertilization and increasing genetic diversity through cross-pollination.

SUBMITTER: Okada T

PROVIDER: S-EPMC5853862 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Project description:Flower signals of bee- and bird-pollinated plants have converged via pollinator-mediated evolution, driven by the visual system of their respective pollinators. For bird flowers, sensory exclusion of less effective bees is also important and such exclusion is also mediated by floral morphological filters. Likewise, other systems based on pollination by red-sensitive insects are also associated with red flowers displaying lower short-wavelength secondary peaks of reflectance, which decreases detectability to animals that are less sensitive to red, such as bees. These flowers often also present long tubes. Here, we tested a generalization of the bee-avoidance hypothesis in order to assess if it holds only for bird flowers or for other non-bee pollination systems as well. For this, we compared flower contrasts and spectral purity in bee visual systems as proxies for conspicuousness among four kinds of pollination systems: bee-visited flowers, insect-visited flowers (including bees and other insects), non-bee insect flowers (flowers visited by red-sensitive insects such as flies, butterflies and beetles, but not bees), and bird-visited flowers. We also assessed the association between conspicuousness to bees and flower depth, used as a proxy for morphological exclusion of bees. Overall, flower conspicuousness to bees differed only between insect (all three groups) and bird flowers, due to lower visual signals for the latter. This suggests that bee sensory exclusion via color signals is exclusive to bird flowers, while non-bee insect flowers might use other sensory channels to exclude bees, such as olfactory signals. Visual bee avoidance might be a mechanism exclusive to plants pollinated by specific guilds of red-sensitive insects not well represented in our sample. We also found a negative association between flower conspicuousness to bees and flower depth, suggesting an interplay of morphological and spectral traits in discouraging bee visits. Our results support the bee-avoidance hypothesis exclusively for bird flowers and an overall association between lower visual signals to bees and long tubes.

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Unfertilized ovary pushes wheat flower open for cross-pollination.

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