Abstract

BackgroundAdaptive radiation theory posits that ecological opportunity promotes rapid proliferation of phylogenetic and ecological diversity. Given that adaptive radiation proceeds via occupation of available niche space in newly accessed ecological zones, theory predicts that: (i) evolutionary diversification follows an ‘early-burst’ process, i.e., it accelerates early in the history of a clade (when available niche space facilitates speciation), and subsequently slows down as niche space becomes saturated by new species; and (ii) phylogenetic branching is accompanied by diversification of ecologically relevant phenotypic traits among newly evolving species. Here, we employ macroevolutionary phylogenetic model-selection analyses to address these two predictions about evolutionary diversification using one of the most exceptionally species-rich and ecologically diverse lineages of living vertebrates, the South American lizard genus Liolaemus.ResultsOur phylogenetic analyses lend support to a density-dependent lineage diversification model. However, the lineage through-time diversification curve does not provide strong support for an early burst. In contrast, the evolution of phenotypic (body size) relative disparity is high, significantly different from a Brownian model during approximately the last 5 million years of Liolaemus evolution. Model-fitting analyses also reject the ‘early-burst’ model of phenotypic evolution, and instead favour stabilizing selection (Ornstein-Uhlenbeck, with three peaks identified) as the best model for body size diversification. Finally, diversification rates tend to increase with smaller body size.ConclusionsLiolaemus have diversified under a density-dependent process with slightly pronounced apparent episodic pulses of lineage accumulation, which are compatible with the expected episodic ecological opportunity created by gradual uplifts of the Andes over the last ~25My. We argue that ecological opportunity can be strong and a crucial driver of adaptive radiations in continents, but may emerge less frequently (compared to islands) when major events (e.g., climatic, geographic) significantly modify environments. In contrast, body size diversification conforms to an Ornstein-Uhlenbeck model with multiple trait optima. Despite this asymmetric diversification between both lineages and phenotype, links are expected to exist between the two processes, as shown by our trait-dependent analyses of diversification. We finally suggest that the definition of adaptive radiation should not be conditioned by the existence of early-bursts of diversification, and should instead be generalized to lineages in which species and ecological diversity have evolved from a single ancestor.Electronic supplementary materialThe online version of this article (doi:10.1186/s12862-015-0435-9) contains supplementary material, which is available to authorized users.

Highlights

  • Adaptive radiation theory posits that ecological opportunity promotes rapid proliferation of phylogenetic and ecological diversity

  • Diversification rates and evolutionary models The results from the Monte Carlo Constant Rate (MCCR) analysis, as shown by the lineage through-time plot (Fig. 2), suggest that lineage accumulation over time in Liolaemus differs from the pattern expected under the null pure-birth model of constant rate diversification (γ = −3.84), but not significantly so (P = 0.13)

  • Our analyses investigating the tempo and mode of evolutionary diversification of one of Earth’s most prolific vertebrate radiations (Liolaemus lizards) reveals a density-dependent pattern of lineage accumulation over time (Fig. 2), while in contrast, the evolution of body size does not follow a traditional pattern of adaptive radiation mode of diversification

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Summary

Introduction

Adaptive radiation theory posits that ecological opportunity promotes rapid proliferation of phylogenetic and ecological diversity. Given that adaptive radiation proceeds via occupation of available niche space in newly accessed ecological zones, theory predicts that: (i) evolutionary diversification follows an ‘early-burst’ process, i.e., it accelerates early in the history of a clade (when available niche space facilitates speciation), and subsequently slows down as niche space becomes saturated by new species; and (ii) phylogenetic branching is accompanied by diversification of ecologically relevant phenotypic traits among newly evolving species. Ecological opportunity arises when spatial and/or ecological dispersal (i.e., access to novel niche dimensions facilitated by adaptive innovations) expose a species to a new set of abundant ecological resources [2,3,4,5,6,7]. A core prediction based on the above scenario is that adaptively radiating lineages will show early bursts of rapid diversification followed by asymptotic decreases in diversification rates over time [2, 8,9,10]

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