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      The Origin of the Legumes is a Complex Paleopolyploid Phylogenomic Tangle Closely Associated with the Cretaceous–Paleogene (K–Pg) Mass Extinction Event

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          Abstract

          The consequences of the Cretaceous–Paleogene (K–Pg) boundary (KPB) mass extinction for the evolution of plant diversity remain poorly understood, even though evolutionary turnover of plant lineages at the KPB is central to understanding assembly of the Cenozoic biota. The apparent concentration of whole genome duplication (WGD) events around the KPB may have played a role in survival and subsequent diversification of plant lineages. To gain new insights into the origins of Cenozoic biodiversity, we examine the origin and early evolution of the globally diverse legume family (Leguminosae or Fabaceae). Legumes are ecologically (co-)dominant across many vegetation types, and the fossil record suggests that they rose to such prominence after the KPB in parallel with several well-studied animal clades including Placentalia and Neoaves. Furthermore, multiple WGD events are hypothesized to have occurred early in legume evolution. Using a recently inferred phylogenomic framework, we investigate the placement of WGDs during early legume evolution using gene tree reconciliation methods, gene count data and phylogenetic supernetwork reconstruction. Using 20 fossil calibrations we estimate a revised timeline of legume evolution based on 36 nuclear genes selected as informative and evolving in an approximately clock-like fashion. To establish the timing of WGDs we also date duplication nodes in gene trees. Results suggest either a pan-legume WGD event on the stem lineage of the family, or an allopolyploid event involving (some of) the earliest lineages within the crown group, with additional nested WGDs subtending subfamilies Papilionoideae and Detarioideae. Gene tree reconciliation methods that do not account for allopolyploidy may be misleading in inferring an earlier WGD event at the time of divergence of the two parental lineages of the polyploid, suggesting that the allopolyploid scenario is more likely. We show that the crown age of the legumes dates to the Maastrichtian or early Paleocene and that, apart from the Detarioideae WGD, paleopolyploidy occurred close to the KPB. We conclude that the early evolution of the legumes followed a complex history, in which multiple auto- and/or allopolyploidy events coincided with rapid diversification and in association with the mass extinction event at the KPB, ultimately underpinning the evolutionary success of the Leguminosae in the Cenozoic. [Allopolyploidy; Cretaceous–Paleogene (K–Pg) boundary; Fabaceae, Leguminosae; paleopolyploidy; phylogenomics; whole genome duplication events]

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          MAFFT Multiple Sequence Alignment Software Version 7: Improvements in Performance and Usability

          We report a major update of the MAFFT multiple sequence alignment program. This version has several new features, including options for adding unaligned sequences into an existing alignment, adjustment of direction in nucleotide alignment, constrained alignment and parallel processing, which were implemented after the previous major update. This report shows actual examples to explain how these features work, alone and in combination. Some examples incorrectly aligned by MAFFT are also shown to clarify its limitations. We discuss how to avoid misalignments, and our ongoing efforts to overcome such limitations.
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            RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies

            Motivation: Phylogenies are increasingly used in all fields of medical and biological research. Moreover, because of the next-generation sequencing revolution, datasets used for conducting phylogenetic analyses grow at an unprecedented pace. RAxML (Randomized Axelerated Maximum Likelihood) is a popular program for phylogenetic analyses of large datasets under maximum likelihood. Since the last RAxML paper in 2006, it has been continuously maintained and extended to accommodate the increasingly growing input datasets and to serve the needs of the user community. Results: I present some of the most notable new features and extensions of RAxML, such as a substantial extension of substitution models and supported data types, the introduction of SSE3, AVX and AVX2 vector intrinsics, techniques for reducing the memory requirements of the code and a plethora of operations for conducting post-analyses on sets of trees. In addition, an up-to-date 50-page user manual covering all new RAxML options is available. Availability and implementation: The code is available under GNU GPL at https://github.com/stamatak/standard-RAxML. Contact: alexandros.stamatakis@h-its.org Supplementary information: Supplementary data are available at Bioinformatics online.
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              Posterior Summarization in Bayesian Phylogenetics Using Tracer 1.7

              Abstract Bayesian inference of phylogeny using Markov chain Monte Carlo (MCMC) plays a central role in understanding evolutionary history from molecular sequence data. Visualizing and analyzing the MCMC-generated samples from the posterior distribution is a key step in any non-trivial Bayesian inference. We present the software package Tracer (version 1.7) for visualizing and analyzing the MCMC trace files generated through Bayesian phylogenetic inference. Tracer provides kernel density estimation, multivariate visualization, demographic trajectory reconstruction, conditional posterior distribution summary, and more. Tracer is open-source and available at http://beast.community/tracer.
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                Author and article information

                Contributors
                Role: Associate Editor
                Journal
                Syst Biol
                Syst Biol
                sysbio
                Systematic Biology
                Oxford University Press
                1063-5157
                1076-836X
                May 2021
                31 August 2020
                31 August 2020
                : 70
                : 3
                : 508-526
                Affiliations
                [1 ] Department of Systematic and Evolutionary Botany, University of Zurich , Zollikerstrasse 107, CH-8008, Zurich, Switzerland
                [2 ] Service Évolution Biologique et Écologie , Faculté des Sciences, Université Libre de Bruxelles, Avenue Franklin Roosevelt 50, 1050, Brussels, Belgium
                [3 ] Norwegian Institute of Bioeconomy Research, Høgskoleveien 8 , 1433 Ås, Norway
                [4 ] Biosystematics Group, Wageningen University & Research , Droevendaalsesteeg 1, 6708 PB, Wageningen, The Netherlands
                [5 ] Naturalis Biodiversity Center , Darwinweg 2, 2333 CR, Leiden, The Netherlands
                [6 ] Royal Botanic Gardens Edinburgh , 20a Inverleith Row, Edinburgh EH3 5LR, UK
                [7 ] School of Biological Sciences, University of Edinburgh, King’s Buildings , Mayfield Rd, Edinburgh, EH9 3JU, UK
                [8 ] Geography, University of Exeter, Amory Building, Rennes Drive , Exeter, EX4 4RJ, UK
                [9 ] Chicago Botanic Garden , 1000 Lake Cook Rd, Glencoe, IL 60022, USA
                [10 ] Institut de Recherche en Biologie Végétale and Département de Sciences Biologiques, Université de Montréal , 4101 Sherbrooke St E, Montreal, QC H1X 2B2, Canada
                Author notes
                Correspondence to be sent to: Department of Systematic and Evolutionary Botany, University of Zurich, Zollikerstrasse 107, CH-8008, Zurich, Switzerland; E-mail: erik.koenen@ 123456systbot.uzh.ch .
                Article
                syaa041
                10.1093/sysbio/syaa041
                8048389
                32483631
                e2f8747d-c3e7-4ddc-b073-cf2f04be5310
                © The Author(s) 2020. Published by Oxford University Press, on behalf of the Society of Systematic Biologists.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contactjournals.permissions@ 123456oup.com

                History
                : 14 February 2020
                : 06 May 2020
                : 25 May 2020
                Page count
                Pages: 24
                Funding
                Funded by: Swiss National Science Foundation, DOI 10.13039/501100001711;
                Award ID: 31003A_135522
                Award ID: 31003A_182453
                Funded by: Department of Systematic & Evolutionary Botany, University of Zurich;
                Funded by: Natural Sciences and Engineering Research Council of Canada, DOI 10.13039/501100000038;
                Funded by: U.K. National Environment Research Council;
                Award ID: NE/I027797/1
                Funded by: Fonds de la Recherche Scientifique of Belgium;
                Award ID: J.0292.17
                Categories
                Regular Articles
                AcademicSubjects/SCI01130

                Animal science & Zoology
                Animal science & Zoology

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