Lactoris Fernandeziana (Lactoridaceae)
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Reconstructing the Basal Angiosperm Phylogeny: Evaluating Information Content of Mitochondrial Genes
55 (4) • November 2006: 837–856 Qiu & al. • Basal angiosperm phylogeny Reconstructing the basal angiosperm phylogeny: evaluating information content of mitochondrial genes Yin-Long Qiu1, Libo Li, Tory A. Hendry, Ruiqi Li, David W. Taylor, Michael J. Issa, Alexander J. Ronen, Mona L. Vekaria & Adam M. White 1Department of Ecology & Evolutionary Biology, The University Herbarium, University of Michigan, Ann Arbor, Michigan 48109-1048, U.S.A. [email protected] (author for correspondence). Three mitochondrial (atp1, matR, nad5), four chloroplast (atpB, matK, rbcL, rpoC2), and one nuclear (18S) genes from 162 seed plants, representing all major lineages of gymnosperms and angiosperms, were analyzed together in a supermatrix or in various partitions using likelihood and parsimony methods. The results show that Amborella + Nymphaeales together constitute the first diverging lineage of angiosperms, and that the topology of Amborella alone being sister to all other angiosperms likely represents a local long branch attrac- tion artifact. The monophyly of magnoliids, as well as sister relationships between Magnoliales and Laurales, and between Canellales and Piperales, are all strongly supported. The sister relationship to eudicots of Ceratophyllum is not strongly supported by this study; instead a placement of the genus with Chloranthaceae receives moderate support in the mitochondrial gene analyses. Relationships among magnoliids, monocots, and eudicots remain unresolved. Direct comparisons of analytic results from several data partitions with or without RNA editing sites show that in multigene analyses, RNA editing has no effect on well supported rela- tionships, but minor effect on weakly supported ones. Finally, comparisons of results from separate analyses of mitochondrial and chloroplast genes demonstrate that mitochondrial genes, with overall slower rates of sub- stitution than chloroplast genes, are informative phylogenetic markers, and are particularly suitable for resolv- ing deep relationships. -
Piperaceae) Revealed by Molecules
Annals of Botany 99: 1231–1238, 2007 doi:10.1093/aob/mcm063, available online at www.aob.oxfordjournals.org From Forgotten Taxon to a Missing Link? The Position of the Genus Verhuellia (Piperaceae) Revealed by Molecules S. WANKE1 , L. VANDERSCHAEVE2 ,G.MATHIEU2 ,C.NEINHUIS1 , P. GOETGHEBEUR2 and M. S. SAMAIN2,* 1Technische Universita¨t Dresden, Institut fu¨r Botanik, D-01062 Dresden, Germany and 2Ghent University, Department of Biology, Research Group Spermatophytes, B-9000 Ghent, Belgium Downloaded from https://academic.oup.com/aob/article/99/6/1231/2769300 by guest on 28 September 2021 Received: 6 December 2006 Returned for revision: 22 January 2007 Accepted: 12 February 2007 † Background and Aims The species-poor and little-studied genus Verhuellia has often been treated as a synonym of the genus Peperomia, downplaying its significance in the relationships and evolutionary aspects in Piperaceae and Piperales. The lack of knowledge concerning Verhuellia is largely due to its restricted distribution, poorly known collection localities, limited availability in herbaria and absence in botanical gardens and lack of material suitable for molecular phylogenetic studies until recently. Because Verhuellia has some of the most reduced flowers in Piperales, the reconstruction of floral evolution which shows strong trends towards reduction in all lineages needs to be revised. † Methods Verhuellia is included in a molecular phylogenetic analysis of Piperales (trnT-trnL-trnF and trnK/matK), based on nearly 6000 aligned characters and more than 1400 potentially parsimony-informative sites which were partly generated for the present study. Character states for stamen and carpel number are mapped on the combined molecular tree to reconstruct the ancestral states. -
Phylogeny, Molecular Dating, and Floral Evolution of Magnoliidae (Angiospermae)
UNIVERSITÉ PARIS-SUD ÉCOLE DOCTORALE : SCIENCES DU VÉGÉTAL Laboratoire Ecologie, Systématique et Evolution DISCIPLINE : BIOLOGIE THÈSE DE DOCTORAT Soutenue le 11/04/2014 par Julien MASSONI Phylogeny, molecular dating, and floral evolution of Magnoliidae (Angiospermae) Composition du jury : Directeur de thèse : Hervé SAUQUET Maître de Conférences (Université Paris-Sud) Rapporteurs : Susanna MAGALLÓN Professeur (Universidad Nacional Autónoma de México) Thomas HAEVERMANS Maître de Conférences (Muséum national d’Histoire Naturelle) Examinateurs : Catherine DAMERVAL Directeur de Recherche (CNRS, INRA) Michel LAURIN Directeur de Recherche (CNRS, Muséum national d’Histoire Naturelle) Florian JABBOUR Maître de Conférences (Muséum national d’Histoire Naturelle) Michael PIRIE Maître de Conférences (Johannes Gutenberg Universität Mainz) Membres invités : Hervé SAUQUET Maître de Conférences (Université Paris-Sud) Remerciements Je tiens tout particulièrement à remercier mon directeur de thèse et ami Hervé Sauquet pour son encadrement, sa gentillesse, sa franchise et la confiance qu’il m’a accordée. Cette relation a immanquablement contribuée à ma progression humaine et scientifique. La pratique d’une science sans frontière est la plus belle chose qu’il m’ait apportée. Ce fut enthousiasmant, très fructueux, et au-delà de mes espérances. Ce mode de travail sera le mien pour la suite de ma carrière. Je tiens également à remercier ma copine Anne-Louise dont le soutien immense a contribué à la réalisation de ce travail. Elle a vécu avec patience et attention les moments d’enthousiasmes et de doutes. Par la même occasion, je remercie ma fille qui a eu l’heureuse idée de ne pas naître avant la fin de la rédaction de ce manuscrit. -
Wood Anatomy and Relationships of Lactoridaceae
WOOD ANATOMY AND RELATIONSHIPS OF LACTORIDACEAE SHERWIN CARLQUIST Made in United States of America Reprinted from AMERICAN JOURNAL OF BOTANY Vol. 77, No. 11. November 1990 Copyright 1990 by the Botanical Society of America, Inc. Amer. J. Bot. 77(11): 1498-1505. 1990. WOOD ANATOMY AND RELATIONSHIPS OF LACTORIDACEAE1 SHERWIN CARLQUIST1 Rancho Santa Ana Botanic Garden and Department of Biology-, Pomona College, Claremont, California 91711 Mature wood of Lactoris, not previously available for study, reveals ten distinctive characters: vessels with simple perforation plates; vessels in pore multiples; vessel-to-axial parenchyma pits scalariform or transitional, vessel-to-vessel pits alternate; fiber-tracheids with vestigial pits; fiber-tracheids, vessels, and axial parenchyma storied; axial parenchyma vasicentric scanty; axial parenchyma either not subdivided or, if subdivided, with thin nonlignified walls between the cells (like the septa in septate fibers); rays wide and tall, little altered during ontogeny; ray cells upright; and ray cells taller adjacent to fascicular areas. All of these features occur in woods of Piper and other Piperaceae. The systematic position of Lactoris is therefore reassessed. Evidence available to date is consonant with placement of Lactoridaceae in Piperales, in which it would be more primitive than Piperaceae or Saururaceae. Features cited as evidence for alternative placements of Lactoridaceae are reviewed. Earlier studies of anatomy of Lactoris fer- variously referred to each of the orders in the nandeziana Phil., sole species of Lactorida superorder Annonanae (for a detailed history ceae, were based on limited material (Carl see Lammers, Stuessy, and Silva O., 1986) quist, 1964). The stems used in that study were Magnoliales (Hutchinson, 1964; Cronquist only twigs, so that the mature wood pattern of 1981; Lammers, Stuessy, and Silva O., 1986) that plant could not be determined. -
Fossil Calibration of Magnoliidae, an Ancient Lineage of Angiosperms
Palaeontologia Electronica palaeo-electronica.org Fossil calibration of Magnoliidae, an ancient lineage of angiosperms Julien Massoni, James Doyle, and Hervé Sauquet ABSTRACT In order to investigate the diversification of angiosperms, an accurate temporal framework is needed. Molecular dating methods thoroughly calibrated with the fossil record can provide estimates of this evolutionary time scale. Because of their position in the phylogenetic tree of angiosperms, Magnoliidae (10,000 species) are of primary importance for the investigation of the evolutionary history of flowering plants. The rich fossil record of the group, beginning in the Cretaceous, has a global distribution. Among the hundred extinct species of Magnoliidae described, several have been included in phylogenetic analyses alongside extant species, providing reliable calibra- tion points for molecular dating studies. Until now, few fossils have been used as cali- bration points of Magnoliidae, and detailed justifications of their phylogenetic position and absolute age have been lacking. Here, we review the position and ages for 10 fos- sils of Magnoliidae, selected because of their previous inclusion in phylogenetic analy- ses of extant and fossil taxa. This study allows us to propose an updated calibration scheme for dating the evolutionary history of Magnoliidae. Julien Massoni. Laboratoire Ecologie, Systématique, Evolution, Université Paris-Sud, CNRS UMR 8079, 91405 Orsay, France. [email protected] James Doyle. Department of Evolution and Ecology, University of California, Davis, CA 95616, USA. [email protected] Hervé Sauquet. Laboratoire Ecologie, Systématique, Evolution, Université Paris-Sud, CNRS UMR 8079, 91405 Orsay, France. [email protected] Keywords: fossil calibration; Canellales; Laurales; Magnoliales; Magnoliidae; Piperales PE Article Number: 18.1.2FC Copyright: Palaeontological Association February 2015 Submission: 10 October 2013. -
Growth Form Evolution in Piperales and Its Relevance
Growth Form Evolution in Piperales and Its Relevance for Understanding Angiosperm Diversification: An Integrative Approach Combining Plant Architecture, Anatomy, and Biomechanics Author(s): Sandrine Isnard, Juliana Prosperi, Stefan Wanke, Sarah T. Wagner, Marie-Stéphanie Samain, Santiago Trueba, Lena Frenzke, Christoph Neinhuis, and Nick P. Rowe Reviewed work(s): Source: International Journal of Plant Sciences, Vol. 173, No. 6 (July/August 2012), pp. 610- 639 Published by: The University of Chicago Press Stable URL: http://www.jstor.org/stable/10.1086/665821 . Accessed: 14/08/2012 12:36 Your use of the JSTOR archive indicates your acceptance of the Terms & Conditions of Use, available at . http://www.jstor.org/page/info/about/policies/terms.jsp . JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact [email protected]. The University of Chicago Press is collaborating with JSTOR to digitize, preserve and extend access to International Journal of Plant Sciences. http://www.jstor.org Int. J. Plant Sci. 173(6):610–639. 2012. Ó 2012 by The University of Chicago. All rights reserved. 1058-5893/2012/17306-0006$15.00 DOI: 10.1086/665821 GROWTH FORM EVOLUTION IN PIPERALES AND ITS RELEVANCE FOR UNDERSTANDING ANGIOSPERM DIVERSIFICATION: AN INTEGRATIVE APPROACH COMBINING PLANT ARCHITECTURE, ANATOMY, AND BIOMECHANICS Sandrine Isnard,1;*,y Juliana Prosperi,z Stefan Wanke,y Sarah T. Wagner,y Marie-Ste´phanie Samain,§ Santiago Trueba,* Lena Frenzke,y Christoph Neinhuis,y and Nick P. -
Molecular Data Place Hydnoraceae with Aristolochiaceae1
American Journal of Botany 89(11): 1809±1817. 2002. MOLECULAR DATA PLACE HYDNORACEAE WITH ARISTOLOCHIACEAE1 DANIEL L. NICKRENT,2 ALBERT BLARER,3 YIN-LONG QIU,4 DOUGLAS E. SOLTIS,5 PAMELA S. SOLTIS,5 AND MICHAEL ZANIS6 2Department of Plant Biology and Center for Systematic Biology, Southern Illinois University, Carbondale, Illinois 62901-6509 USA; 3Institute of Systematic Botany, University of Zurich, Zollikerstrasse 107, 8008 Zurich, Switzerland; 4Department of Biology, Morrill Science Center, University of Massachusetts, Amherst, Massachusetts 01003-5810 USA; 5Department of Botany, University of Florida, Gainesville, Florida 32611-8526 USA; and 6Department of Biology, Washington State University, Pullman, Washington 99164-4236 USA Utilization of molecular phylogenetic information over the past decade has resulted in clari®cation of the position of most angio- sperms. In contrast, the position of the holoparasitic family Hydnoraceae has remained controversial. To address the question of phylogenetic position of Hydnoraceae among angiosperms, nuclear SSU and LSU rDNA and mitochondrial atp1 and matR sequences were obtained for Hydnora and Prosopanche. These sequences were used in combined analyses that included the above four genes as well as chloroplast rbcL and atpB (these plastid genes are missing in Hydnoraceae and were hence coded as missing). Three data sets were analyzed using maximum parsimony: (1) three genes with 461 taxa; (2) ®ve genes with 77 taxa; and (3) six genes with 38 taxa. Analyses of separate and combined data partitions support the monophyly of Hydnoraceae and the association of that clade with Aristolochiaceae sensu lato (s.l.) (including Lactoridaceae). The latter clade is sister to Piperaceae and Saururaceae. Despite over 11 kilobases (kb) of sequence data, relationships within Aristolochiaceae s.l. -
LETTER Doi:10.1038/Nature12872
LETTER doi:10.1038/nature12872 Three keys to the radiation of angiosperms into freezing environments Amy E. Zanne1,2, David C. Tank3,4, William K. Cornwell5,6, Jonathan M. Eastman3,4, Stephen A. Smith7, Richard G. FitzJohn8,9, Daniel J. McGlinn10, Brian C. O’Meara11, Angela T. Moles6, Peter B. Reich12,13, Dana L. Royer14, Douglas E. Soltis15,16,17, Peter F. Stevens18, Mark Westoby9, Ian J. Wright9, Lonnie Aarssen19, Robert I. Bertin20, Andre Calaminus15, Rafae¨l Govaerts21, Frank Hemmings6, Michelle R. Leishman9, Jacek Oleksyn12,22, Pamela S. Soltis16,17, Nathan G. Swenson23, Laura Warman6,24 & Jeremy M. Beaulieu25 Early flowering plants are thought to have been woody species to greater heights: as path lengths increase so too does resistance5. restricted to warm habitats1–3. This lineage has since radiated into Among extant strategies, the most efficient method of water delivery almost every climate, with manifold growth forms4. As angiosperms is through large-diameter water-conducting conduits (that is, vessels spread and climate changed, they evolved mechanisms to cope with and tracheids) within xylem5. episodic freezing. To explore the evolution of traits underpinning Early in angiosperm evolution they probably evolved larger conduits the ability to persist in freezing conditions, we assembled a large for water transport, especially compared with their gymnosperm cousins14. species-level database of growth habit (woody or herbaceous; 49,064 Although efficient in delivering water, these larger cells would have species), as well as leaf phenology (evergreen or deciduous), diameter impeded angiosperm colonization of regions characterized by episodic of hydraulic conduits (that is, xylem vessels and tracheids) and climate freezing14,15, as the propensity for freezing-induced embolisms (air bub- occupancies (exposure to freezing). -
Ancestral Traits and Specializations in the Flowers of the Basal Grade of Living Angiosperms
Zurich Open Repository and Archive University of Zurich Main Library Strickhofstrasse 39 CH-8057 Zurich www.zora.uzh.ch Year: 2015 Ancestral traits and specializations in the flowers of the basal grade of living angiosperms Endress, Peter K ; Doyle, James A DOI: https://doi.org/10.12705/646.1 Posted at the Zurich Open Repository and Archive, University of Zurich ZORA URL: https://doi.org/10.5167/uzh-119333 Journal Article Published Version Originally published at: Endress, Peter K; Doyle, James A (2015). Ancestral traits and specializations in the flowers of the basal grade of living angiosperms. Taxon, 64(6):1093-1116. DOI: https://doi.org/10.12705/646.1 TAXON 64 (6) • December 2015: 1093–1116 Endress & Doyle • Flowers of basal living angiosperms REVIEW Ancestral traits and specializations in the flowers of the basal grade of living angiosperms Peter K. Endress1 & James A. Doyle2 1 Department of Systematic Botany, University of Zurich, Zollikerstrasse 107, 8008 Zurich, Switzerland 2 Department of Evolution and Ecology, University of California, Davis, California 95616, U.S.A. Author for correspondence: Peter K. Endress, [email protected] ORCID: PKE, http://orcid.org/000166228196; JAD, http://orcid.org/000240838786 DOI http://dx.doi.org/10.12705/646.1 Abstract New morphological and phylogenetic data prompt us to present an updated review of floral morphology and its evolution in the basal ANITA grade of living angiosperms, Chloranthaceae, and Ceratophyllum. Floral phyllotaxis is complex whorled in Nymphaeales and spiral in Amborella and Austrobaileyales. It is unresolved whether phyllotaxis was ancestrally whorled or spiral, but if it was whorled, the whorls were trimerous. -
Placing the Monocots: Conflicting Signal from Trigenomic Analyses Melvin R
Aliso: A Journal of Systematic and Evolutionary Botany Volume 22 | Issue 1 Article 7 2006 Placing the Monocots: Conflicting Signal from Trigenomic Analyses Melvin R. Duvall Northern Illinois University Sarah Matthews Harvard University Neill Mohammad University of Michigan Tammy Russel Northern Illinois University Follow this and additional works at: http://scholarship.claremont.edu/aliso Part of the Botany Commons Recommended Citation Duvall, Melvin R.; Matthews, Sarah; Mohammad, Neill; and Russel, Tammy (2006) "Placing the Monocots: Conflicting Signal from Trigenomic Analyses," Aliso: A Journal of Systematic and Evolutionary Botany: Vol. 22: Iss. 1, Article 7. Available at: http://scholarship.claremont.edu/aliso/vol22/iss1/7 Basal Monocots ~£?t~QCOTSogy and Evolution Excluding Poales Aliso 22, pp. 79-90 © 2006, Rancho Santa Ana Botanic Garden PLACING THE MONOCOTS: CONFLICTING SIGNAL FROM TRIGENOMIC ANALYSES 1 3 MELVIN R. DUVALL, ,4 SARAH MATHEWS,2 NEILL MOHAMMAD, AND TAMMY RUSSELL 1 1Department of Biological Sciences, Northern Illinois University, DeKalb, Illinois 60115, USA; 2The Arnold Arboretum of Harvard University, 22 Divinity Avenue, Cambridge, Massachusetts 02138, USA; 3Department of Political Science, University of Michigan, Ann Arbor, Michigan 48109, USA 4Corresponding author ([email protected]) ABSTRACT Despite recent significant advances in understanding angiosperm phylogeny, the position of mono cots remains uncertain. We present here a phylogeny inferred from four genes that unambiguously unite monocots with eumagnoliids. A well-supported position for the monocots was obtained only after we replaced the available nuclear 18S rDNA sequence data with data from phytochrome C in a matrix that also included plastid rbcL and ndhF and mitochondrial atp 1. Over 5000 base pairs of sequence data from 42 taxa were analyzed using Bayesian inference. -
Phylogenetic Analysis of Magnoliales and Myristicaceae Based on Multiple Data Sets: Implications for Character Evolution
Blackwell Science, LtdOxford, UKBOJBotanical Journal of the Linnean Society0024-4074The Linnean Society of London, 2003? 2003 1422 125186 Original Article PHYLOGENETICS OF MAGNOLIALES H. SAUQUET ET AL Botanical Journal of the Linnean Society, 2003, 142, 125–186. With 14 figures Phylogenetic analysis of Magnoliales and Myristicaceae based on multiple data sets: implications for character evolution HERVÉ SAUQUET1*, JAMES A. DOYLE2, TANYA SCHARASCHKIN2, THOMAS BORSCH3, KHIDIR W. HILU4, LARS W. CHATROU5 and ANNICK LE THOMAS1 1Laboratoire de Biologie et Évolution des Plantes vasculaires EPHE, Muséum national d’Histoire naturelle, 16, rue Buffon, 75005 Paris, France 2Section of Evolution and Ecology, University of California, Davis, CA 95616, USA 3Abteilung Systematik und Biodiversität, Botanisches Institut und Botanischer Garten, Friedrich- Wilhelms-Universität Bonn, Meckenheimer Allee 170, 53115 Bonn, Germany 4Department of Biology, Virginia Tech, Blacksburg, VA 24061, USA 5National Herbarium of the Netherlands, Utrecht University branch, Heidelberglaan 2, 3584 CS Utrecht, The Netherlands Received September 2002; accepted for publication January 2003 Magnoliales, consisting of six families of tropical to warm-temperate woody angiosperms, were long considered the most archaic order of flowering plants, but molecular analyses nest them among other eumagnoliids. Based on sep- arate and combined analyses of a morphological matrix (115 characters) and multiple molecular data sets (seven variable chloroplast loci and five more conserved genes; 14 536 aligned nucleotides), phylogenetic relationships were investigated simultaneously within Magnoliales and Myristicaceae, using Laurales, Winterales, and Piperales as outgroups. Despite apparent conflicts among data sets, parsimony and maximum likelihood analyses of combined data converged towards a fully resolved and well-supported topology, consistent with higher-level molecular analyses except for the position of Magnoliaceae: Myristicaceae + (Magnoliaceae + ((Degeneria + Galbulimima) + (Eupomatia + Annonaceae))). -
Three Keys to the Radiation of Angiosperms Into Freezing Environments
LETTER doi:10.1038/nature12872 Three keys to the radiation of angiosperms into freezing environments Amy E. Zanne1,2, David C. Tank3,4, William K. Cornwell5,6, Jonathan M. Eastman3,4, Stephen A. Smith7, Richard G. FitzJohn8,9, Daniel J. McGlinn10, Brian C. O’Meara11, Angela T. Moles6, Peter B. Reich12,13, Dana L. Royer14, Douglas E. Soltis15,16,17, Peter F. Stevens18, Mark Westoby9, Ian J. Wright9, Lonnie Aarssen19, Robert I. Bertin20, Andre Calaminus15, Rafae¨l Govaerts21, Frank Hemmings6, Michelle R. Leishman9, Jacek Oleksyn12,22, Pamela S. Soltis16,17, Nathan G. Swenson23, Laura Warman6,24 & Jeremy M. Beaulieu25 Early flowering plants are thought to have been woody species to greater heights: as path lengths increase so too does resistance5. restricted to warm habitats1–3. This lineage has since radiated into Among extant strategies, the most efficient method of water delivery almost every climate, with manifold growth forms4. As angiosperms is through large-diameter water-conducting conduits (that is, vessels spread and climate changed, they evolved mechanisms to cope with and tracheids) within xylem5. episodic freezing. To explore the evolution of traits underpinning Early in angiosperm evolution they probably evolved larger conduits the ability to persist in freezing conditions, we assembled a large for water transport, especially compared with their gymnosperm cousins14. species-level database of growth habit (woody or herbaceous; 49,064 Although efficient in delivering water, these larger cells would have species), as well as leaf phenology (evergreen or deciduous), diameter impeded angiosperm colonization of regions characterized by episodic of hydraulic conduits (that is, xylem vessels and tracheids) and climate freezing14,15, as the propensity for freezing-induced embolisms (air bub- occupancies (exposure to freezing).