Abstract

A striking characteristic of the Western North American flora is the repeated evolution of hummingbird pollination from insect‐pollinated ancestors. This pattern has received extensive attention as an opportunity to study repeated trait evolution as well as potential constraints on evolutionary reversibility, with little attention focused on the impact of these transitions on species diversification rates. Yet traits conferring adaptation to divergent pollinators potentially impact speciation and extinction rates, because pollinators facilitate plant reproduction and specify mating patterns between flowering plants. Here, we examine macroevolutionary processes affecting floral pollination syndrome diversity in the largest North American genus of flowering plants, Penstemon. Within Penstemon, transitions from ancestral bee‐adapted flowers to hummingbird‐adapted flowers have frequently occurred, although hummingbird‐adapted species are rare overall within the genus. We inferred macroevolutionary transition and state‐dependent diversification rates and found that transitions from ancestral bee‐adapted flowers to hummingbird‐adapted flowers are associated with reduced net diversification rate, a finding based on an estimated 17 origins of hummingbird pollination in our sample. Although this finding is congruent with hypotheses that hummingbird adaptation in North American Flora is associated with reduced species diversification rates, it contrasts with studies of neotropical plant families where hummingbird pollination has been associated with increased species diversification. We further used the estimated macroevolutionary rates to predict the expected pattern of floral diversity within Penstemon over time, assuming stable diversification and transition rates. Under these assumptions, we find that hummingbird‐adapted species are expected to remain rare due to their reduced diversification rates. In fact, current floral diversity in the sampled Penstemon lineage, where less than one‐fifth of species are hummingbird adapted, is consistent with predicted levels of diversity under stable macroevolutionary rates.

Highlights

  • An important goal of evolutionary biology is to understand processes that determine trait diversity within groups of related species

  • The FiSSE analysis on this dataset corroborates this conclusion: the inverse equal splits speciation rate for bee syndrome species is greater than that for hummingbird syndrome species ( 0 = 2.56, 1 = 2.06), a difference that is significantly larger than expected if diversification rate is not associated with pollination syndrome (P = .018)

  • Our study necessarily simplifies over this complexity to examine how pollination syndrome in particular impacts diversification

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Summary

Introduction

An important goal of evolutionary biology is to understand processes that determine trait diversity within groups of related species. Flowers adapted to hummingbird pollinators have evolved many independent times in North American flowering plants from insectpollinated ancestors, providing an excellent example of convergent evolution. This pattern suggests the evolution of hummingbird-adapted flowers has often been favored. Other examples include the evolution of host specialization in bark beetles, the evolution of sociality in spiders, and the evolution of asexuality (Kelley and Farrell 1998; Agnarsson et al 2006; Schwander and Crespi 2009) This pattern of rarity despite high rates of transition to the derived state can lead to a phylogenetic pattern of “tippiness,” as well documented for certain transitions in flower color (Ng and Smith 2018)

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