Is a new and general theory of molecular systematics emerging?
Open accessAbstract
The advent and maturation of algorithms for estimating species trees-phylogenetic trees that allow gene tree heterogeneity and whose tips represent lineages, populations and species, as opposed to genes-represent an exciting confluence of phylogenetics, phylogeography, and population genetics, and ushers in a new generation of concepts and challenges for the molecular systematist. In this essay I argue that to better deal with the large multilocus datasets brought on by phylogenomics, and to better align the fields of phylogeography and phylogenetics, we should embrace the primacy of species trees, not only as a new and useful practical tool for systematics, but also as a long-standing conceptual goal of systematics that, largely due to the lack of appropriate computational tools, has been eclipsed in the past few decades. I suggest that phylogenies as gene trees are a "local optimum" for systematics, and review recent advances that will bring us to the broader optimum inherent in species trees. In addition to adopting new methods of phylogenetic analysis (and ideally reserving the term "phylogeny" for species trees rather than gene trees), the new paradigm suggests shifts in a number of practices, such as sampling data to maximize not only the number of accumulated sites but also the number of independently segregating genes; routinely using coalescent or other models in computer simulations to allow gene tree heterogeneity; and understanding better the role of concatenation in influencing topologies and confidence in phylogenies. By building on the foundation laid by concepts of gene trees and coalescent theory, and by taking cues from recent trends in multilocus phylogeography, molecular systematics stands to be enriched. Many of the challenges and lessons learned for estimating gene trees will carry over to the challenge of estimating species trees, although adopting the species tree paradigm will clarify many issues (such as the nature of polytomies and the star tree paradox), raise conceptually new challenges, or provide new answers to old questions.
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Heterogeneity in the topology of gene trees is expected to occur, especially during rapid radiations.
“Heterogeneity in the topology of gene trees is expected to occur, especially during rapid radiations (Edwards 2009).”
From Bayesian Detection of Convergent Rate Changes of Conserved Noncoding Elements on Phylogenetic Trees (2019) · cites this paper as Edwards 2009
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Broad phylogenomic sampling improves resolution of the animal tree of life
Dunn, C. W., Hejnol, A., Matus, D. Q., Pang, K., Browne, W. E., Smith, S. A., Seaver, E., Rouse, G. W., Obst, M., Edgecombe, G. D., et al. (2008) · Nature · doi:10.1038/nature06614 · Cited by 1,921 · cited 1× · see citing works
“Recent phylogenomic analyses have begun to enshrine the concatenation paradigm by amassing hundreds of genes to unravel the Tree of Life (e.g., Rokas et al. 2003; Delsuc et al. 2006; Dunn et al. 2008; reviewed in Delsuc et al. 2005).”
BackgroundGenome-scale approaches to resolving incongruence in molecular phylogenies.
Rokas, A., Williams, B. L., King, N., & Carroll, S. B. (2003) · Nature · doi:10.1038/nature02053 · Cited by 1,512 · see citing works
Resolution of Phylogenetic Conflict in Large Data Sets by Increased Taxon Sampling
Hedtke, S. M., Townsend, T. M., & Hillis, D. M. (2006) · Systematic Biology · doi:10.1080/10635150600697358 · Cited by 303 · see citing works
Branch-length prior influences Bayesian posterior probability of phylogeny.
Yang, Z., & Rannala, B. (2005) · Systematic Biology · doi:10.1080/10635150590945313 · Cited by 228 · see citing works
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Research works printed but not linked: 26
- ---. 2000. Phylogeography: the history and formation of Species. Harvard Univ. Press, Cambridge, MA.
- Avise, J. C., and R. M. J. Ball. 1990. Principles of genealogical concordance in species concepts and biological taxonomy. Oxford Sur. Evol. Biol. 7:45-67.
- Avise, J. C., and K. Wollenberg. 1997. Phylogenetics and the origin of species. Proc. Natl. Acad. Sci. USA 94:7748-7755.
- Avise, J. C., J. Arnold, R. M. Ball, E. Bermingham, T. Lamb, J. E. Neigel, C. A. Reeb, and N. C. Saunders. 1987. Intraspecific phylogeography: the mi- tochondrial DNA bridge between population genetics and systematics. Ann. Rev. Ecol. Syst. 18:489-522.
- Brito, P., and S. Edwards. 2008. Multilocus phylogeography and phylogenet- ics using sequence-based markers. Genetica. doi: 10.1007/s10709-008- 9293-3. · DOI
- Cavalli-Sforza, L. L. 1964. Population structure and human evolution. Proc. R. Soc. Lond. B 164:362-379.
- ---. 2008. Gene tree discordance, phylogenetic inference, and the multi- species coalescent. Trends Ecol. Evol. in press.
- Degnan, J. H., M. DeGiorgio, D. Bryant, and N. A. Rosenberg. 2008. Coales- cent consequences for consensus cladograms. Syst. Biol. in press.
- de Queiroz, K. 2005. Ernst Mayr and the modern concept of species. Proc. Natl. Acad. Sci. USA 102:6600-6607.
- Doolittle, W. F., and E. Bapteste. 2007. Pattern pluralism and the Tree of Life hypothesis. Proc. Natl. Acad. Sci. USA 104:2043-2049.
- Edwards, S. V., S. B. Kingan, J. D. Calkins, C. N. Balakrishnan, W. B. Jennings, W. J. Swanson, and M. D. Sorenson. 2005. Speciation in birds: genes, geography, and sexual selection. Proc. Natl. Acad. Sci. USA 102(Supp 1):6550-6557.
- Edwards, S. V., L. Liu, and D. K. Pearl. 2007. High-resolution species trees without concatenation. Proc. Natl. Acad. Sci. USA 104:5936-5941.
- Janes, D. E., T. Ezaz, J. A. Marshall Graves, and S. V. Edwards. 2008. Re- combination and nucleotide diversity in the sex chromosomal pseudoau- tosomal region of the Emu, Dromaius novaehollandiae. J. Hered. doi: "10.1093/jhered/esn065". · DOI
- Kluge, A. G. 1983. Cladistics and the classification of great apes. Pp. 151-177
- Liu, L., and S. V. Edwards. 2008. Phylogenetic analysis in the anomaly zone. Manuscript, Cambridge, MA.
- Liu, L., and D. K. Pearl. 2006. Species trees from gene trees: reconstruct- ing posterior distributions of a species phylogeny using estimated gene tree distributions. Pp. 24. Mathematical Biosciences Institute Technical Report #53. Ohio State Univ., Columbus.
- Mossel, E., and S. Roch. 2007. Incomplete lineage sorting: con- sistent phylogeny estimation from multiple loci. Available at http://arxiv.org/abs/0710.0262. · arXiv
- Nei, M., and S. Kumar. 2000. Molecular evolution and phylogenetics. Oxford Univ. Press, New York.
- Neigel, J. E., and J. C. Avise. 1986. Phylogenetic relationships of mitochon- drial DNA under various demographic models of speciation. Pp. 515- 534 in S. Karlin, and E. Nevo, eds. Evolutionary processes and theory. Academic Press, New York.
- O'Meara, B. C. 2008. Using trees: myrmecocystus phylogeny and character evolution and new methods for investigating trait evolution and species delimitation (Ph.D. Dissertation). Available from Nature Proceedings http://dx.doi.org/10.1038/npre.2008.2261. · DOI
- Otto, S. P., M. P. Cummings, and J. Wakeley. 1996. Inferring phylogenies from DNA sequence data: the effects of sampling. Pp. 103-115 in P. H. Harvey, A. J. Leigh Brown, J. Maynard Smith, and S. Nee, eds. New Uses for new Phylogenies. Oxfore University Press, New York.
- Seo, T. K., H. Kishino, and J. L. Thorne. 2005. Incorporating gene-specific variation when inferring and evaluating optimal evolutionary tree topolo- gies from multilocus sequence data. Proc. Natl. Acad. Sci. USA 102:4436-4441.
- Suzuki, Y., G. V. Glazko, and M. Nei. 2002. Overcredibility of molecular phylogenies obtained by Bayesian phylogenetics. Proc. Natl. Acad. Sci. USA 99:16138-16143.
- Swofford, D. L., G. J. Olsen, P. J. Waddell, and D. M. Hillis. 1996. Phylo- genetic inference. Pp. 407-514 in D. M. Hillis, C. Moritz, and B. K. Mable, eds. Molecular Systematics, 2nd ed. Sinauer, Sunderland, MA.
- Thomson, R. C., A. M. Shedlock, S. V. Edwards, and H. B. Shaf- fer. 2008. Developing markers for multilocus phylogenetics in non- model organisms: a test case with turtles. Mol. Phylogenet. Evol. doi: 10.1016/j.ympev.2008.08.006. · DOI
- ---. 2002. MCMCcoal: Markov Chain Monte Carlo Coalescent Program, version 1.0. Pp. 8, Oxford.
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Shen, X.-X., Hittinger, C. T., & Rokas, A. (2017) · Nature Ecology & Evolution · doi:10.1038/s41559-017-0126 · Cited by 520 · see citing works
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- Authors
- Edwards, S. V.
- Affiliations
- Harvard University (US)
- Corresponding author
- Edwards, Scott V.
- ORCID
- Edwards, Scott V.
- Venue
- Evolution
- Publisher
- Oxford University Press (OUP)
- Published
- 2009-01
- Volume
- 63
- Issue
- 1
- Pages
- 1-19
- ISSN
- 0014-3820 (ISSN-L)
- 1558-5646
- OpenAlex
- W2037654474
- Cited by
- 1,040
- References
- 4
- Citations by year
- 2026: 26 · 2025: 39 · 2024: 30 · 2023: 42 · 2022: 44 · 2021: 54 · 2020: 52 · 2019: 65 · 2018: 63 · 2017: 67 · 2016: 56 · 2015: 81 · 2014: 90 · 2013: 100 · 2012: 81
- FWCI
- 19.00
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Evolution (publishedVersion)
- PubMed (publishedVersion)
- Digital Access to Scholarship at Harvard (DASH) (Harvard University) (submittedVersion, cc-by)
- BioOne Complete (BioOne) (submittedVersion)
- Funders
- National Science Foundation (0743616)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic diversity and population structure
- Physical Sciences › Earth and Planetary Sciences › Paleontology › Evolution and Paleontology Studies
- Keywords
- species tree, gene tree heterogeneity, molecular systematics, phylogenomics, coalescent theory, gene tree estimation, polytomies, phylogenetic systematics
- MeSH terms
- Classification, Genes, Models, Genetic, Phylogeny, Genetic Variation, Polymorphism, Single Nucleotide, Genetic Speciation
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