4.6 Article

Diversity and evolution of a trait mediating ant-plant interactions: insights from extrafloral nectaries in Senna (Leguminosae)

Journal

ANNALS OF BOTANY
Volume 111, Issue 6, Pages 1263-1275

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/aob/mcs226

Keywords

Antplant mutualism; ant protection; extrafloral nectaries; Senna; Fabaceae; functional morphology; homology; key innovation; morphological evolution; ontogeny; phylogeny

Categories

Funding

  1. Swiss National Science Foundation [PA00P3-126248]
  2. National Geographic Research Program [8775-10]
  3. Swiss National Science Foundation (SNF) [PA00P3_126248] Funding Source: Swiss National Science Foundation (SNF)

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Plants display a wide range of traits that allow them to use animals for vital tasks. To attract and reward aggressive ants that protect developing leaves and flowers from consumers, many plants bear extrafloral nectaries (EFNs). EFNs are exceptionally diverse in morphology and locations on a plant. In this study the evolution of EFN diversity is explored by focusing on the legume genus Senna, in which EFNs underwent remarkable morphological diversification and occur in over 80 of the approx. 350 species. EFN diversity in location, morphology and plant ontogeny was characterized in wild and cultivated plants, using scanning electron microscopy and microtome sectioning. From these data EFN evolution was reconstructed in a phylogenetic framework comprising 83 Senna species. Two distinct kinds of EFNs exist in two unrelated clades within Senna. Individualized EFNs (iEFNs), located on the compound leaves and sometimes at the base of pedicels, display a conspicuous, gland-like nectary structure, are highly diverse in shape and characterize the species-rich EFN clade. Previously overlooked non-individualized EFNs (non-iEFNs) embedded within stipules, bracts, and sepals are cryptic and may represent a new synapomorphy for clade II. Leaves bear EFNs consistently throughout plant ontogeny. In one species, however, early seedlings develop iEFNs between the first pair of leaflets, but later leaves produce them at the leaf base. This ontogenetic shift reflects our inferred diversification history of iEFN location: ancestral leaves bore EFNs between the first pair of leaflets, while leaves derived from them bore EFNs either between multiple pairs of leaflets or at the leaf base. EFNs are more diverse than previously thought. EFN-bearing plant parts provide different opportunities for EFN presentation (i.e. location) and individualization (i.e. morphology), with implications for EFN morphological evolution, EFNant protective mutualisms and the evolutionary role of EFNs in plant diversification.

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