The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.
Extant timetrees are consistent with a myriad of diversification histories
Open accessAbstract
Time-calibrated phylogenies of extant species (referred to here as ‘extant timetrees’) are widely used for estimating diversification dynamics1. However, there has been considerable debate surrounding the reliability of these inferences2–5 and, to date, this critical question remains unresolved. Here we clarify the precise information that can be extracted from extant timetrees under the generalized birth–death model, which underlies most existing methods of estimation. We prove that, for any diversification scenario, there exists an infinite number of alternative diversification scenarios that are equally likely to have generated any given extant timetree. These ‘congruent’ scenarios cannot possibly be distinguished using extant timetrees alone, even in the presence of infinite data. Importantly, congruent diversification scenarios can exhibit markedly different and yet similarly plausible dynamics, which suggests that many previous studies may have over-interpreted phylogenetic evidence. We introduce identifiable and easily interpretable variables that contain all available information about past diversification dynamics, and demonstrate that these can be estimated from extant timetrees. We suggest that measuring and modelling these identifiable variables offers a more robust way to study historical diversification dynamics. Our findings also make it clear that palaeontological data will continue to be crucial for answering some macroevolutionary questions. An infinite number of alternative diversification scenarios—which may have markedly different, but equally plausible, dynamics—can underpin a given time-calibrated phylogeny of extant species, suggesting many previous studies have over-interpreted phylogenetic evidence.
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Cites
The biodiversity of species and their rates of extinction, distribution, and protection
Pimm, S. L., Jenkins, C. N., Abell, R., Brooks, T. M., Gittleman, J. L., Joppa, L. N., Raven, P. H., Roberts, C. M., & Sexton, J. O. (2014) · Science · doi:10.1126/science.1246752 · Cited by 3,542
Impacts of the Cretaceous Terrestrial Revolution and KPg extinction on mammal diversification
Meredith, R. W., Janečka, J. E., Gatesy, J., Ryder, O. A., Fisher, C. A., Teeling, E. C., Goodbla, A., Eizirik, E., Simão, T. L. L., Stadler, T., et al. (2011) · Science · doi:10.1126/science.1211028 · Cited by 1,464
A Selected Core Microbiome Drives the Early Stages of Three Popular Italian Cheese Manufactures
De Filippis, F., La Storia, A., Stellato, G., Gatti, M., & Ercolini, D. (2014) · PLoS ONE · doi:10.1371/journal.pone.0089680 · Cited by 1,398
The fossilized birth-death process for coherent calibration of divergence-time estimates
Heath, T. A., Huelsenbeck, J. P., & Stadler, T. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1319091111 · Cited by 834
Efficient comparative phylogenetics on large trees
Louca, S., & Doebeli, M. (2018) · Bioinformatics · doi:10.1093/bioinformatics/btx701 · Cited by 564
Self-citationMass extinctions and macroevolution
Jablonski, D. (2005) · Paleobiology · doi:10.1666/0094-8373(2005)031[0192:meam]2.0.co;2 · Cited by 317
Five palaeobiological laws needed to understand the evolution of the living biota
Marshall, C. R. (2017) · Nature Ecology & Evolution · doi:10.1038/s41559-017-0165 · Cited by 231
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Gardner, J. D., & Organ, C. L. (2021) · Systematic Biology · doi:10.1093/sysbio/syab017 · Cited by 21
Metadata
- Authors
- Louca, S., & Pennell, M. W.
- Venue
- Nature
- Published
- 2020-04-15
- Volume
- 580
- Issue
- 7804
- Pages
- 502-505
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W3016352084
- Cited by
- 502
- References
- 7
- FWCI
- 48.53
- Type
- journal article
- Language
- en
- Open access
- green
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