Abstract

Phenotypic traits are often integrated into evolutionary modules: sets of organismal parts that evolve together. In social insect colonies, the concepts of integration and modularity apply to sets of traits both within and among functionally and phenotypically differentiated castes. On macroevolutionary timescales, patterns of integration and modularity within and across castes can be clues to the selective and ecological factors shaping their evolution and diversification. We develop a set of hypotheses describing contrasting patterns of worker integration and apply this framework in a broad (246 species) comparative analysis of major and minor worker evolution in the hyperdiverse ant genus Pheidole. Using geometric morphometrics in a phylogenetic framework, we inferred fast and tightly integrated evolution of mesosoma shape between major and minor workers, but slower and more independent evolution of head shape between the two worker castes. Thus, Pheidole workers are evolving as a mixture of intracaste and intercaste integration and rate heterogeneity. The decoupling of homologous traits across worker castes may represent an important process facilitating the rise of social complexity.

Highlights

  • The increase of morphological complexity following divergence in cellular function is a repeating theme in the evolution of multicellular organisms (Wagner and Altenberg 1996)

  • In comparisons of similar traits between worker castes, we observed no significant differences in evolutionary rate for head shape or mesosoma shape

  • Patterns of macroevolutionary integration and modularity within and among castes may provide clues to the selective forces shaping diversification in ants, and the developmental biases and constraints involved in trait divergence (West-Eberhard 1979)

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Summary

Introduction

The increase of morphological complexity following divergence in cellular function is a repeating theme in the evolution of multicellular organisms (Wagner and Altenberg 1996). Given cues regarding their developmental fate, cells and tissues express their identical genomes in different ways to produce different traits and allow functional specialization. Eusocial insects reflect a major evolutionary transition whereby a unit of selection is comprised of different individuals working together as part of an integrated colony-level phenotype (Wheeler 1911; Hölldobler and Wilson 1990; Szathmáry and Smith 1995) and understanding the evolution and function of these “superorganisms” is a major and enduring interest of evolutionary biology

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