Phylogenetic comparative methods

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Phylogenetic comparative methods Will Cornwell, Shinichi Nakagawa  Current Biology  Volume 27, Issue 9, Pages R333-R336 (May 2017) DOI: 10.1016/j.cub.2017.03.049 Copyright © 2017 Elsevier Ltd Terms and Conditions

Figure 1 An example use of a PCM for understanding trait evolution. Werner and colleagues were interested in the evolution of the ability to form nitrogen-fixing symbioses among angiosperms. The symbionts of the individual plant taxa differ, and are traditionally grouped into two types: rhizobial and actinorhizal associations. The ability to form such symbioses is only found is a small set of species, which are located within the ‘nitrogen-fixing clade’. The authors reconstructed the evolution of the trait using a PCM that included the possibility of the evolution of an unknown precursor to the actual trait; the red arrows connect the precusor to the places in the phylogeny where PCMs infer the final evolution of the symbioses. The PCM used strongly supports a pathway to nitrogen fixation via a single precursor that evolved only once in the history of angiosperm evolution. They estimated when this precursor evolved (about 100 million years ago) and which extant clades should still have the precursor but not the ability to form a nitrogen-fixing symbiosis. The identity of this precursor is still unknown and is an area of active research. Figures modified and adopted from Werner et al. (2014). Current Biology 2017 27, R333-R336DOI: (10.1016/j.cub.2017.03.049) Copyright © 2017 Elsevier Ltd Terms and Conditions

Figure 2 An example of lineage-diversification PCMs. Lineage-diversification PCMs can simultaneously estimate the rates of transition among different groups, speciation, and extinction. In an analysis of bird-feeding guilds, Burin and colleagues used a PCM that found omnivores to be an ‘evolutionary sink’ — that is, there are significant transitions into that class from many others, but relatively infrequent transitions out of that class. The rates of transitions are represented by the thickness of lines. Within omnivores, the PCM also reconstructed a relatively high rate of extinction. Simultaneously understanding trait evolution, speciation, and extinction is one of the keys to understanding adaptive radiations across all taxa. Figure modified and adopted from Burin et al. (2016). Current Biology 2017 27, R333-R336DOI: (10.1016/j.cub.2017.03.049) Copyright © 2017 Elsevier Ltd Terms and Conditions

Figure 3 Applications of PCMs to anthropological questions. (A) Transitions between different political states, with thick solid arrows indicating high transition rates, narrow solid arrows indicating moderate to low rates, and thin dotted arrows representing extremely low rates (or virtually zero transition). (B) Correlated evolution between ritual human sacrifice and social stratification with pie charts at nodes representing probabilities of different states at these ancestral nodes. Figures simplified and adapted from Currie et al. (2010) and Watts et al. (2016). Current Biology 2017 27, R333-R336DOI: (10.1016/j.cub.2017.03.049) Copyright © 2017 Elsevier Ltd Terms and Conditions