2021
DOI: 10.1016/j.cub.2021.05.050
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Pollen transport: Illuminating a key mechanism of disassortative pollination

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Cited by 3 publications
(2 citation statements)
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“…On the other hand, ovules are protected within the ovary and, excepting cases of flower predation or abiotic stresses, their fate is mainly determined by the quantity and quality of the pollen received on a flower's stigma and available resources to mature seeds and fruits (Harder and Routley, 2006). Because of such disparate uncertainties (Wilson et al, 1994), pollen grains frequently outnumber ovules by several orders of magnitude, and different flower traits can be subjected to strong male‐biased selection for increasing pollen export (Minnaar et al, 2019; Karron et al, 2021), including floral display size (Sutherland and Delph, 1984; Sutherland, 1987; Campbell, 1989) and pollen production itself (Cruden, 2000; Cunha et al, 2022).…”
Section: Discussionmentioning
confidence: 99%
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“…On the other hand, ovules are protected within the ovary and, excepting cases of flower predation or abiotic stresses, their fate is mainly determined by the quantity and quality of the pollen received on a flower's stigma and available resources to mature seeds and fruits (Harder and Routley, 2006). Because of such disparate uncertainties (Wilson et al, 1994), pollen grains frequently outnumber ovules by several orders of magnitude, and different flower traits can be subjected to strong male‐biased selection for increasing pollen export (Minnaar et al, 2019; Karron et al, 2021), including floral display size (Sutherland and Delph, 1984; Sutherland, 1987; Campbell, 1989) and pollen production itself (Cruden, 2000; Cunha et al, 2022).…”
Section: Discussionmentioning
confidence: 99%
“…Our results suggest a link between floral display size and per‐flower pollen production that can be interpreted within the framework of massive pollen losses occurring during the transport of pollen from anthers to stigmas, which in animal‐pollinated flowering plants averages 98.4%, ranging between 51.65 and 99.99% (N. L. da Cunha and M. A. Aizen, unpublished data). Also, the evolutionary effect on pollen production of these pollen transfer losses (Morgan, 1992; Harder and Wilson, 1998; Karron et al, 2021) and post‐pollination pollen mortality due to pistil rejection (Swanson et al, 2004; Broz and Bedinger, 2021) can be observed in the average 20% difference in the number of pollen grains produced by the flowers of self‐compatible vs. self‐incompatible species (Appendix S1, Figure S2B), which can be attributed to differences in self‐pollination and selfing capacity (Hirayama et al, 2005; Brys et al, 2016; Harder and Johnson, 2023 [this issue]). While plants with larger floral displays may benefit from increasing pollinator attraction, they pay the cost of increasing geitonogamous pollination and thus increasing pollen discounting (Barrett et al, 1996; Harder and Wilson, 1998).…”
Section: Discussionmentioning
confidence: 99%