Abstract

Adaptive radiation is a common mode of speciation among plants endemic to oceanic islands. This pattern is one of cladogenesis, or splitting of the founder population, into diverse lineages in divergent habitats. In contrast, endemic species have also evolved primarily by simple transformations from progenitors in source regions. This is anagenesis, whereby the founding population changes genetically and morphologically over time primarily through mutation and recombination. Gene flow among populations is maintained in a homogeneous environment with no splitting events. Genetic consequences of these modes of speciation have been examined in the Juan Fernández Archipelago, which contains two principal islands of differing geological ages. This article summarizes population genetic results (nearly 4000 analyses) from examination of 15 endemic species, involving 1716 and 1870 individuals in 162 and 163 populations (with amplified fragment length polymorphisms and simple sequence repeats, respectively) in the following genera: Drimys (Winteraceae), Myrceugenia (Myrtaceae), Rhaphithamnus (Verbenaceae), Robinsonia (Asteraceae, Senecioneae) and Erigeron (Asteraceae, Astereae). The results indicate that species originating anagenetically show high levels of genetic variation within the island population and no geographic genetic partitioning. This contrasts with cladogenetic species that show less genetic diversity within and among populations. Species that have been derived anagenetically on the younger island (1-2 Ma) contain less genetic variation than those that have anagenetically speciated on the older island (4 Ma). Genetic distinctness among cladogenetically derived species on the older island is greater than among similarly derived species on the younger island. An important point is that the total genetic variation within each genus analysed is comparable, regardless of whether adaptive divergence occurs.

Highlights

  • Oceanic islands have long stimulated biologists to investigate patterns and processes of evolution (e.g. Darwin 1842; Wallace 1881; Whittaker and Fernandez-Palacios 2007; Bramwell and Caujape -Castells 2011)

  • The results from analysis of species that have evolved anagenetically include those from Myrceugenia fernandeziana, M. schulzei, Robinsonia masafuerae, D. confertifolia and R. venustus

  • In D. confertifolia, and R. venustus, which occur on both islands, one sees in both cases more genetic diversity (SDI) in populations on the older island than on the younger island except for estimates of simple sequence repeats (SSRs) in R. venustus (Table 1)

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Summary

Introduction

Oceanic islands have long stimulated biologists to investigate patterns and processes of evolution (e.g. Darwin 1842; Wallace 1881; Whittaker and Fernandez-Palacios 2007; Bramwell and Caujape -Castells 2011). One dimension of speciation in island plants that has received considerable attention is adaptive radiation (Carlquist 1974; Whittaker and Fernandez-Palacios 2007; Rundell and Price 2009) This is a process that begins with dispersal from the original immigrant population into different habitats on the same or neighbouring island. This isolation leads to divergence of the new segregate populations, each becoming rapidly adapted to divergent habitats (Schluter 2001), such that eventually new species are recognized taxonomically. A number of dramatic species complexes have developed in oceanic islands through adaptive radiation, such as illustrated by the lobelioids (Givnish et al 2009) and silverswords (Carlquist et al 2003) in Hawaii, Aeonium (Liu 1989; Jorgensen and Olesen 2001) and Echium (Bohle et al 1996) in the Canary Islands and Scalesia (Eliasson 1974) in the Galapagos archipelago

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