Abstract
Reticulate evolution often leads to incongruence between nuclear and plastid phylogenies, and comparisons between them have been used as a first approximation to disentangle patterns of hybridization. Because other processes like incomplete lineage sorting and phylogenetic error also produce similar incongruence patterns, additional sources of evidence must be incorporated. Here we focus on reconstructing the phylogeny of Lachemilla (Rosaceae) using nuclear ribosomal ITS and plastid trnL-FDNAsequences, and explore widespread patterns of cytonuclear discordance in this group. Lachemilla is a highly morphologically variable group of perennial herbs and shrubs, and a nearly ubiquitous member of the diverse Neotropical high-altitude grasslands. Our analyses identified four major clades within Lachemilla that are in part congruent with previous morphological classifications of the group. Furthermore, using multiple sources of evidence, including a procrustean approach to cophylogeny estimation, coalescent-based simulations, phylogenetic networks, chromosome counts, and genome size estimations, we also revealed a large-scale pattern of incongruence between the plastid and nuclear phylogenies in Lachemilla, which is mainly the result of widespread hybridization and polyploidy.We also estimated that the origin of Lachemilla in South America (;14.5 MYA) predates the "rapid-uplift" diversification model that has been suggested for other high species-richness Andean plant clades, but following the formation of the high-elevation Andean grasslands during the last 5 MYA, a rapid accumulation of particular nested lineages has contributed to the ubiquitous presence of Lachemilla in these biomes.
Original language | English |
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Pages (from-to) | 17-34 |
Number of pages | 18 |
Journal | Systematic Botany |
Volume | 43 |
Issue number | 1 |
DOIs | |
State | Published - Apr 2018 |
Bibliographical note
Publisher Copyright:© 2018 by the American Society of Plant Taxonomists.
Funding
Acknowledgments. We are grateful to the curators of ANDES, CR, HAO, LPB, MEXU, and QCA for local assistance. We would like to thank Simon Uribe-Convers and Pedro Tenorio-Lezama for assistance during fieldwork. We are indebted to Petr Sklenárˇ for assistance with the flow cytometry. We would like to thank Ya Yang, two anonymous reviewers, and members of the Tank Lab at the University of Idaho for providing helpful comments on earlier versions of the manuscript. This work was funded in part by the Pontificia Universidad Católica del Ecuador, a Secretaría de Educación Superior, Ciencia, Tecnología e Innovación del Ecuador (SENESCYT) Doctoral scholarship to DFM-B, Graduate Student Research Grants from the Botanical Society of America, American Society of Plant Taxonomists, International Association of Plant Taxonomists, and the University of Idaho Stillinger Herbarium Expedition Funds to DFM-B, and a National Science Foundation Doctoral Dissertation Improvement Grant to DCT for DFM-B (DEB-1502049).
Funders | Funder number |
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International Association of Plant Taxonomists | |
National Science Foundation | DEB-1502049 |
American Society of Plant Taxonomists | |
Botanical Society of America | |
Secretaría de Educación Superior, Ciencia, Tecnología e Innovación | |
Pontifical Catholic University of Ecuador |
Keywords
- Andes
- cpDNA
- hybridization
- nrDNA
- paramo
- polyploidy