Abstract

SynopsisDespite longstanding interest in convergent evolution, factors that result in deviations from fully convergent phenotypes remain poorly understood. In birds, the evolution of flightless wing-propelled diving has emerged as a classic example of convergence, having arisen in disparate lineages including penguins (Sphenisciformes) and auks (Pan-Alcidae, Charadriiformes). Nevertheless, little is known about the functional anatomy of the wings of flightless auks because all such taxa are extinct, and their morphology is almost exclusively represented by skeletal remains. Here, in order to re-evaluate the extent of evolutionary convergence among flightless wing-propelled divers, wing muscles and ligaments were reconstructed in two extinct flightless auks, representing independent transitions to flightlessness: Pinguinus impennis (a crown-group alcid), and Mancalla (a stem-group alcid). Extensive anatomical data were gathered from dissections of 12 species of extant charadriiforms and 4 aequornithine waterbirds including a penguin. The results suggest that the wings of both flightless auk taxa were characterized by an increased mechanical advantage of wing elevator/retractor muscles, and decreased mobility of distal wing joints, both of which are likely advantageous for wing-propelled diving and parallel similar functional specializations in penguins. However, the conformations of individual muscles and ligaments underlying these specializations differ markedly between penguins and flightless auks, instead resembling those in each respective group’s close relatives. Thus, the wings of these flightless wing-propelled divers can be described as convergent as overall functional units, but are incompletely convergent at lower levels of anatomical organization—a result of retaining differing conditions from each group’s respective volant ancestors. Detailed investigations such as this one may indicate that, even in the face of similar functional demands, courses of phenotypic evolution are dictated to an important degree by ancestral starting points.

Highlights

  • Convergent evolution, defined as acquired similarity between distantly-related lineages, has been regarded as evidence for the predictability of organismal evolution under natural selection (e.g., Conway Morris 2003, 2010; Melville et al 2006; Mahler et al 2013)

  • The evolution of avian wing-propelled diving provides a classic example of convergent evolution

  • The extant charadriiform taxa used as the basis for reconstructing the musculature of the extinct flightless auks showed little variation in the positions of osteological correlates of major wing muscles and ligaments

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Summary

Introduction

Convergent evolution, defined as acquired similarity between distantly-related lineages, has been regarded as evidence for the predictability of organismal evolution under natural selection (e.g., Conway Morris 2003, 2010; Melville et al 2006; Mahler et al 2013). Convergence may arise as a result of a tight relationship between phenotype and functional performance, and/or evolutionary constraints or biases inherent to certain organismal designs that result in a limitation of possible phenotypic solutions (Wake 1991; Losos 2011; Wake et al 2011). These factors often operate simultaneously, and may lead to nonidentical outcomes because of differences in ancestral conditions and/or evolvability between lineages (historical contingency; e.g., Gould 2002; Agrawal 2017; Blount et al 2018). Some petrels and shearwaters (Procellariidae), gannets (Sulidae), and certain waterfowl (Anatidae) are known to use their wings, sometimes along with their feet, in underwater movement (e.g., Townsend 1909; Kuroda 1954; Storer 1960; Ashmole 1971)

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