Volume 22, Issue 12
Letter

Understanding the effect of competition during evolutionary radiations: an integrated model of phenotypic and species diversification

Leandro Aristide

Corresponding Author

E-mail address: leandroaristi@gmail.com

École Normale Supérieure, Paris Sciences et Lettres (PSL) Research University, Institut de Biologie de l’École Normale Supérieure (IBENS), CNRS, UMR 8197, INSERM U1024, 46 rue d’Ulm, F‐75005 Paris, France

Correspondence: E‐mail: leandroaristi@gmail.com

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Hélène Morlon

École Normale Supérieure, Paris Sciences et Lettres (PSL) Research University, Institut de Biologie de l’École Normale Supérieure (IBENS), CNRS, UMR 8197, INSERM U1024, 46 rue d’Ulm, F‐75005 Paris, France

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First published: 10 September 2019
Citations: 9

Abstract

Competition can drive macroevolutionary change, for example during adaptive radiations. However, we still lack a clear understanding of how it shapes diversification processes and patterns. To better understand the macroevolutionary consequences of competition, as well as the signal left on phylogenetic data, we developed a model linking trait evolution and species diversification in an ecological context. We find four main results: first, competition spurs trait diversity but not necessarily species richness; second, competition produces slowdowns in species diversification even in the absence of explicit ecological limits, but not in phenotypic diversification even in the presence of such limits; third, early burst patterns do not provide a reliable way of testing for adaptive radiations; and fourth, looking for phylogenetic signal in trait data and support for phenotypic models incorporating competition is a better alternative. Our results clarify the macroevolutionary consequences of competition and could help design more powerful tests of adaptive radiations in nature.

Number of times cited according to CrossRef: 9

  • Inhibition of p62/SQSTM1 sensitizes small‐cell lung cancer cells to cisplatin‐induced cytotoxicity by targeting NEDD9 expression, Molecular Carcinogenesis, 10.1002/mc.23215, 59, 8, (967-979), (2020).
  • Dietary morphology of two island-endemic murid rodent clades is consistent with persistent, incumbent-imposed competitive interactions, Proceedings of the Royal Society B: Biological Sciences, 10.1098/rspb.2019.2746, 287, 1921, (20192746), (2020).
  • Diversification in evolutionary arenas—Assessment and synthesis, Ecology and Evolution, 10.1002/ece3.6313, 10, 12, (6163-6182), (2020).
  • Angiosperms at the edge: Extremity, diversity, and phylogeny, Plant, Cell & Environment, 10.1111/pce.13887, 0, 0, (2020).
  • High-throughput sequencing for community analysis: the promise of DNA barcoding to uncover diversity, relatedness, abundances and interactions in spider communities, Development Genes and Evolution, 10.1007/s00427-020-00652-x, (2020).
  • Assessing the causes of diversification slowdowns: temperature‐dependent and diversity‐dependent models receive equivalent support, Ecology Letters, 10.1111/ele.13382, 22, 11, (1900-1912), (2019).
  • Estimating Diversity Through Time Using Molecular Phylogenies: Old and Species-Poor Frog Families are the Remnants of a Diverse Past, Systematic Biology, 10.1093/sysbio/syz057, (2019).
  • Nitrate Concentration Trends in Iowa's Rivers, 1998 to 2012: What Challenges Await Nutrient Reduction Initiatives?, Journal of Environmental Quality, 10.2134/jeq2013.03.0111, 42, 6, (1822-1828), (2013).
  • Science, Policy, and Management of Irrigation‐Induced Selenium Contamination in California, Journal of Environmental Quality, 10.2134/jeq2013.04.0154, 42, 6, (1605-1614), (2013).

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