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RODRIGUEZ Rafael Lucas

  • , University of Wisconsin-Milwaukee, Milwaukee, United States of America
  • Adaptation, Behavior & Social Evolution, Phenotypic Plasticity, Sexual Selection, Speciation
  • recommender

Recommendations:  0

Review:  1

Areas of expertise
2013 – present Associate Professor (tenured) Univ. of Wisconsin–Milwaukee 2007 – 2012 Assistant Professor Univ. of Wisconsin–Milwaukee 2002 – 2006 Post–doctoral Fellow Univ. of Missouri PhD, 2002 Univ. of Kansas Ecology & Evolutionary Biology, Entomology MS, 1996 Univ. of Costa Rica Biology BS, 1991 Univ. of Costa Rica Biology

Review:  1

29 Nov 2023
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Does sociality affect evolutionary speed?

On the evolutionary implications of being a social animal

Recommended by based on reviews by Rafael Lucas Rodriguez and 1 anonymous reviewer

What does it mean to be highly social?  Considering the so-called four ‘pinnacles’ of animal society (Wilson, 1975) – humans, cooperative breeding as found in some non-human mammals and birds, the social insects, and colonial marine invertebrates – having inter-individual relations extending beyond the sexual pair and the parent-offspring interaction is foremost.  In many cases being social implies a high local population density, interaction with the same group of individuals over an extended time period, and an overlapping of generations.  Additional features of social species may be a wide geographical range, perhaps associated with ecological and behavioral plasticity, the latter often facilitated by cultural transmission of traditions.  

Narrowing our perspective to the domain of PCI Evolutionary Biology, we might continue our question by asking whether being social predisposes one to a special evolutionary path toward the future.  Do social species evolve faster (or slower) than their more solitary relatives such that over time they are more unlike (or similar to) those relatives (anagenesis)?  And are evolutionary changes in social species more or less likely to be accompanied by lineage splitting (cladogenesis) and ultimately speciation?  The latter question is parallel to one first posed over 40 years ago (West-Eberhard, 1979; Lande, 1981) for sexually selected traits:  Do strong mating preferences and conspicuous courtship signals generate speciation via the Fisherian process or ecological divergence?  An extensive survey of birds had found little supporting evidence (Price, 1998), but a recent one that focused on plumage complexity in tanagers did reveal a relationship, albeit a weak one (Price-Waldman et al., 2020).  Because sexual selection has been viewed as a part of the broader process of social selection (West-Eberhard, 1979), it is thus fitting to extend our surveys to the evolutionary implications of being social.

Unlike the inquiry for a sexual selection - evolutionary change connection, a social behavior counterpart has remained relatively untreated.  Diverse logistical problems might account for this oversight.  What objective proxies can be used for social behavior, and for the rate of evolutionary change within a lineage?  How many empirical studies have generated data from which appropriate proxies could be extracted?  More intractable is the conundrum arising from the connectedness between socially- and sexually-selected traits.  For example, the elevated population density found in highly social species can greatly increase the mating advantage enjoyed by an attractive male.  If anagenesis is detected, did it result from social behavior or sexual selection?  And if social behavior leads to a group structure in which male-male competition is reduced, would a modest rate of evolutionary change be support for the sexual selection - evolutionary speed connection or evidence opposing the sociality - evolution one?

Against the above odds, several biologists have begun to explore the notion that social behavior just might favor evolutionary speed in either anagenesis or cladogenesis.  In a recent analysis relying on the comparative method, Lluís Socias-Martínez and Louise Rachel Peckre (2023) combed the scientific literature archives and identified those studies with specific data on the relationships between sexual selection or social behavior and evolutionary change, either anagenesis or cladogenesis.  The authors were careful to employ fairly conservative criteria for including studies, and the number eventually retained was small.  Nonetheless, some patterns emerge:  Many more studies report anagenesis than cladogenesis, and many more report correlations with sexually-selected traits than with non-sexual social behavior ones.  And, no study indicates a potential effect of social behavior on cladogenesis.  Is this latter observation authentic or an artifact of a paucity of data?  There are some a priori reasons why cladogenesis may seldom arise.  Whereas highly social behavior could lead to fission encompassing mutually isolated population clusters within a species, social behavior may also engender counterbalancing plasticity that allows and even promotes inter-cluster migration and fusion.  And briefly – and non-systematically, as the rate of lineage splitting would need to be measured – looking at one of the pinnacles of animal social behavior, the social insects, there is little indication that diversification has been accelerated.  There are fewer than 3000 described species of termites, only ca. 16,000 ants, and the vast majority of bees and wasps are solitary.                            

Lluís Socias-Martínez and Louise Rachel Peckre provide us with a very detailed discussion of these and a myriad of other complications.  I end with a common refrain, we need more consideration of the authors’ interesting question, and much more data and analysis.  One can thank Socias-Martínez and Peckre for pointing us in that direction.

References

Lande, R. (1981). Models of speciation by sexual selection on polygenic traits. Proc. Natn. Acad. Sci. USA 78, 3721-3725. https://doi.org/10.1073/pnas.78.6.3721

Price, T. (1998). Sexual selection and natural selection in bird speciation. Phil. Trans. Roy. Soc. B, 353, 251-260.  https://doi.org/10.1098/rstb.1998.0207  

Price‐Waldman, R. M., Shultz, A. J., & Burns, K. J. (2020). Speciation rates are correlated with changes in plumage color complexity in the largest family of songbirds. Evolution, 74(6), 1155–1169. https://doi.org/10.1111/evo.13982

Socias-Martínez and Peckre. (2023). Does sociality affect evolutionary speed? Zenodo, ver. 3 peer-reviewed and recommended by Peer Community in Evolutionary Biology. https://doi.org/10.5281/zenodo.10086186

West-Eberhard, M. J. (1979). Sexual selection, social competition, and evolution. Proceedings of the American Philosophical Society, 123(4), 222–234. http://www.jstor.org/stable/2828804

Wilson, E. O. (1975). Sociobiology. The New Synthesis. Cambridge, Mass., The Belknap Press of Harvard University

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RODRIGUEZ Rafael Lucas

  • , University of Wisconsin-Milwaukee, Milwaukee, United States of America
  • Adaptation, Behavior & Social Evolution, Phenotypic Plasticity, Sexual Selection, Speciation
  • recommender

Recommendations:  0

Review:  1

Areas of expertise
2013 – present Associate Professor (tenured) Univ. of Wisconsin–Milwaukee 2007 – 2012 Assistant Professor Univ. of Wisconsin–Milwaukee 2002 – 2006 Post–doctoral Fellow Univ. of Missouri PhD, 2002 Univ. of Kansas Ecology & Evolutionary Biology, Entomology MS, 1996 Univ. of Costa Rica Biology BS, 1991 Univ. of Costa Rica Biology