Plastome data reveal multiple geographic origins of Quercus Group Ilex

Department of Agricultural and Forestry Science (DAFNE), Università degli Studi della Tuscia, 01100 Viterbo, Italy
Department of Palaeontology, University of Wien, 1090 Wien, Austria
Dipartimento di Biologia, Università degli studi di Firenze, 50121 Firenze, Italy
Department of Life Science, Università degli studi di Trieste, 34127 Trieste, Italy
Stazione Zoologica Anton Dohrn, 8012 Napoli, Italy
INRA, UMR BIOGECO-1202, F-33612 Cestas, France
UMR BIOGECO-1202, Université Bordeaux, F-33405 Talence, France
Department of Palaeobiology, Swedish Museum of Natural History, 10405 Stockholm, Sweden
DOI
10.7287/peerj.preprints.1615v1
Subject Areas
Biogeography, Ecology, Evolutionary Studies, Plant Science
Keywords
Fagaceae, Mediterranean, Plastome polyphyly, Ancient introgression, Incomplete lineage sorting, Decoupled phylogenies
Copyright
© 2015 Simeone et al.
Licence
This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ PrePrints) and either DOI or URL of the article must be cited.
Cite this article
Simeone MC, Grimm GW, Papini A, Vessella F, Cardoni S, Tordoni E, Piredda R, Franc A, Denk T. 2015. Plastome data reveal multiple geographic origins of Quercus Group Ilex. PeerJ PrePrints 3:e1615v1

Abstract

Nucleotide sequences from the plastome are currently the main source for assessing taxonomic and phylogenetic relationships in flowering plants and their historical biogeography at all hierarchical levels. One exception is the large and economically important genus Quercus (oaks). Whereas differentiation patterns of the nuclear genome are in agreement with morphology and the fossil record, diversity patterns in the plastome are at odds with established taxonomic and phylogenetic relationships. However, the extent and evolutionary implications of this incongruence has yet to be fully uncovered. The DNA sequence divergence of four Euro-Mediterranean Group Ilex oak species (Quercus ilex L., Q. coccifera L., Q. aucheri Jaub. & Spach., Q. alnifolia Poech.) was explored at three chloroplast markers (rbcL, trnK-matK, trnH-psbA). Phylogenetic relationships were reconstructed including worldwide members of additional 55 species representing all Quercus subgeneric groups. Family and order sequence data were harvested from gene banks to better frame the observed divergence in larger taxonomic contexts. We found a strong geographic sorting in the focal group and the genus in general that is entirely decoupled from species boundaries. Main plastid haplotypes shared by distinct oak lineages from the same geographic region and high plastid diversity in members of Group Ilex are indicative for a polyphyletic origin of their plastomes. The results suggest that incomplete lineage sorting and repeated phases of unidirectional introgression among ancestral lineages of Group Ilex and two other main Groups of Eurasian oaks (Cyclobalanopsis and Cerris) caused this complex pattern. Comparison with the current phylogenetic synthesis also suggests an initial high- versus mid-latitude biogeographic split within Quercus. High plastome plasticity of Group Ilex reflects geographic area disruptions, possibly linked with high tectonic activity of past and modern distribution ranges, that did not leave imprints in the nuclear genome of modern species and infrageneric lineages.

Author Comment

This is a submission to PeerJ for review.

Supplemental Information

List of specimens investigated

DOI: 10.7287/peerj.preprints.1615v1/supp-1

Plastome divergence in Fagales

Intra- and intertaxonomic minimum and maximum pairwise genetic distances in Fagales based on the used plastid markers

DOI: 10.7287/peerj.preprints.1615v1/supp-2

RbcL and trnK-matK haplotype networks

haplotype networks of the investigated dataset based on rbcL and trnK-matK markers

DOI: 10.7287/peerj.preprints.1615v1/supp-3