The DOI matches its Crossref record; 12 of the 12 references it cites were found in a registry or an index.
Land plant evolutionary timeline: Gene effects are secondary to fossil constraints in relaxed clock estimation of age and substitution rates
Abstract
• Premise of the study: Land plants play an essential role in the evolution of terrestrial life. Their time of origin and diversification is fundamental to understanding the evolution of life on land. We investigated the timing and the rate of molecular evolution of land plants, evaluating the effects of different types of molecular data, including temporal information from fossils, and using different molecular clock methods. • Methods: Ages and absolute rates were estimated independently with two substitutionally different data sets: a highly conserved 4‐gene data set and matK, a fast‐evolving gene. The vascular plant backbone and the crown nodes of all major lineages were calibrated with fossil‐derived ages. Dates and absolute rates were estimated while including or excluding the calibrations and using two relaxed clocks that differ in their implementation of temporal autocorrelation. • Key results: Land plants diverged from streptophyte alga 912 (870–962) million years ago (Mya) but diversified into living lineages 475 (471–480) Mya. Ages estimated for all major land‐plant lineages agree with their fossil record, except for angiosperms. Different genes estimated very similar ages and correlated absolute rates across the tree. Excluding calibrations resulted in the greatest age differences. Different relaxed clocks provided similar ages, but different and uncorrelated absolute rates. • Conclusions: Whole‐genome rate accelerations or decelerations may underlie the similar ages and correlated absolute rates estimated with different genes. We suggest that pronounced substitution rate changes around the angiosperm crown node may represent a challenge for relaxed clocks to model adequately.
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Cites
RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models
Stamatakis, A. (2006) · Bioinformatics · doi:10.1093/bioinformatics/btl446 · Cited by 15,582
Relaxed Phylogenetics and Dating with Confidence
Drummond, A. J., Ho, S. Y. W., Phillips, M. J., & Rambaut, A. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040088 · Cited by 6,463
Sanderson, M. J. (2002) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a003974 · Cited by 1,977
Sanderson, M. J. (2003) · Bioinformatics · doi:10.1093/bioinformatics/19.2.301 · Cited by 1,906
Paleontological Evidence to Date the Tree of Life
Benton, M. J., & Donoghue, P. C. J. (2006) · Molecular Biology and Evolution · doi:10.1093/molbev/msl150 · Cited by 916
A molecular timescale of eukaryote evolution and the rise of complex multicellular life
Hedges, S. B., Blair, J. E., Venturi, M. L., & Shoe, J. L. (2004) · BMC Evolutionary Biology · doi:10.1186/1471-2148-4-2 · Cited by 578
A general comparison of relaxed molecular clock models
Lepage, T., Bryant, D., Philippe, H., & Lartillot, N. (2007) · Molecular Biology and Evolution · doi:10.1093/molbev/msm193 · Cited by 546
Inferring speciation times under an episodic molecular clock
Rannala, B., & Yang, Z. (2007) · Systematic Biology · doi:10.1080/10635150701420643 · Cited by 475
Rocks and clocks: calibrating the Tree of Life using fossils and molecules
Donoghue, P. C. J., & Benton, M. J. (2007) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2007.05.005 · Cited by 413
Molecular and fossil evidence on the origin of angiosperms
Doyle, J. A. (2012) · Annual Review of Earth and Planetary Sciences · doi:10.1146/annurev-earth-042711-105313 · Cited by 239
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Self-citationThe Interrelationships of Land Plants and the Nature of the Ancestral Embryophyte
Puttick, M. N., Morris, J. L., Williams, T. A., Cox, C. J., Edwards, D., Kenrick, P., Pressel, S., Wellman, C. H., Schneider, H., Pisani, D., et al. (2018) · Current Biology · doi:10.1016/j.cub.2018.01.063 · Cited by 498
Vanneste, K., Baele, G., Maere, S., & Van de Peer, Y. (2014) · Genome Research · doi:10.1101/gr.168997.113 · Cited by 444
Revisiting Criteria for Plant MicroRNA Annotation in the Era of Big Data
Axtell, M. J., & Meyers, B. C. (2018) · The Plant Cell · doi:10.1105/tpc.17.00851 · Cited by 429
The Apostasia genome and the evolution of orchids
Zhang, G.-Q., Liu, K.-W., Li, Z., Lohaus, R., Hsiao, Y.-Y., Niu, S.-C., Wang, J.-Y., Lin, Y.-C., Xu, Q., Chen, L.-J., et al. (2017) · Nature · doi:10.1038/nature23897 · Cited by 408
Metadata
- Authors
- Magallón, S., Hilu, K. W., & Quandt, D.
- Venue
- American Journal of Botany
- Publisher
- Wiley
- Published
- 2013-03
- Volume
- 100
- Issue
- 3
- Pages
- 556-573
- ISSN
- 0002-9122 (ISSN-L)
- 1537-2197
- OpenAlex
- W2145697624
- Cited by
- 318
- References
- 12
- FWCI
- 41.28
- Type
- journal article
- Language
- en
- Open access
- closed
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- Magallón, S., Hilu, K. W., & Quandt, D. (2013). Land plant evolutionary timeline: Gene effects are secondary to fossil constraints in relaxed clock estimation of age and substitution rates. American Journal of Botany. https://doi.org/10.3732/ajb.1200416
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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