Abstract

The interaction between floral traits and reproductive isolation is crucial to explaining the extraordinary diversity of angiosperms. Heterostyly, a complex floral polymorphism that optimizes outcrossing, evolved repeatedly and has been shown to accelerate diversification in primroses, yet its potential influence on isolating mechanisms remains unexplored. Furthermore, the relative contribution of pre‐ versus postmating barriers to reproductive isolation is still debated. No experimental study has yet evaluated the possible effects of heterostyly on pre‐ and postmating reproductive mechanisms. We quantify multiple reproductive barriers between the heterostylous Primula elatior (oxlip) and P. vulgaris (primrose), which readily hybridize when co‐occurring, and test whether traits of heterostyly contribute to reproductive barriers in unique ways. We find that premating isolation is key for both species, while postmating isolation is considerable only for P. vulgaris; ecogeographic isolation is crucial for both species, while phenological, seed developmental, and hybrid sterility barriers are also important in P. vulgaris, implicating sympatrically higher gene flow into P. elatior. We document for the first time that, in addition to the aforementioned species‐dependent asymmetries, morph‐dependent asymmetries affect reproductive barriers between heterostylous species. Indeed, the interspecific decrease of reciprocity between high sexual organs of complementary floral morphs limits interspecific pollen transfer from anthers of short‐styled flowers to stigmas of long‐styled flowers, while higher reciprocity between low sexual organs favors introgression over isolation from anthers of long‐styled flowers to stigmas of short‐styled flowers. Finally, intramorph incompatibility persists across species boundaries, but is weakened in long‐styled flowers of P. elatior, opening a possible backdoor to gene flow through intramorph pollen transfer between species. Therefore, patterns of gene flow across species boundaries are likely affected by floral morph composition of adjacent populations. To summarize, our study highlights the general importance of premating isolation and newly illustrates that both morph‐ and species‐dependent asymmetries shape boundaries between heterostylous species.

Highlights

  • The interaction between floral traits and reproductive isolation is crucial to explaining angiosperm diversity

  • We find that premating isolation is key for both species, while postmating isolation is considerable only for P. vulgaris; ecogeographic isolation is crucial for both species, while phenological, seed developmental, and hybrid sterility barriers are important in P. vulgaris, implicating sympatrically higher gene flow into P. elatior

  • Ecology and Evolution published by John Wiley & Sons Ltd

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Summary

Introduction

The interaction between floral traits and reproductive isolation is crucial to explaining angiosperm diversity. A decrease of sexual organ reciprocity (as observed in Primula; Keller et al 2012) might restrict interspecific pollen movement between reciprocal morphs, hypothetically contributing to mechanical isolation (Haller et al 2014). If the difference of pollen exchange between exposed and sunken organs is maintained interspecifically and the significantly lower number of ovules than pollen grains in angiosperms is considered (e.g., in distylous primroses: Ornduff 1979; Schou 1983; Piper and Charlesworth 1986), selection to restrict access of interspecific pollen to ovules might be stronger on the L- than S-morph, increasing mechanical isolation in the former over the latter, a prediction tested in this study. In order to examine the specific contributions of heterostyly to reproductive isolation, we assess a series of preand postmating barriers between P. elatior and P. vulgaris at different stages of the life cycle, including ecogeographic characteristics, flowering phenology, and pollen transfer between parental species, as well as formation, survivorship, and reproduction of hybrids. This study represents the first, in-depth analysis of the special means by which heteromorphy in hermaphroditic flowers might modulate gene flow between species

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