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The Linderniaceae and Gratiolaceae Are Further Lineages Distinct from the Scrophulariaceae (Lamiales)
Research Paper 1 The Linderniaceae and Gratiolaceae are further Lineages Distinct from the Scrophulariaceae (Lamiales) R. Rahmanzadeh1, K. Müller2, E. Fischer3, D. Bartels1, and T. Borsch2 1 Institut für Molekulare Physiologie und Biotechnologie der Pflanzen, Universität Bonn, Kirschallee 1, 53115 Bonn, Germany 2 Nees-Institut für Biodiversität der Pflanzen, Universität Bonn, Meckenheimer Allee 170, 53115 Bonn, Germany 3 Institut für Integrierte Naturwissenschaften ± Biologie, Universität Koblenz-Landau, Universitätsstraûe 1, 56070 Koblenz, Germany Received: July 14, 2004; Accepted: September 22, 2004 Abstract: The Lamiales are one of the largest orders of angio- Traditionally, Craterostigma, Lindernia and their relatives have sperms, with about 22000 species. The Scrophulariaceae, as been treated as members of the family Scrophulariaceae in the one of their most important families, has recently been shown order Lamiales (e.g., Takhtajan,1997). Although it is well estab- to be polyphyletic. As a consequence, this family was re-classi- lished that the Plocospermataceae and Oleaceae are their first fied and several groups of former scrophulariaceous genera branching families (Bremer et al., 2002; Hilu et al., 2003; Soltis now belong to different families, such as the Calceolariaceae, et al., 2000), little is known about the evolutionary diversifica- Plantaginaceae, or Phrymaceae. In the present study, relation- tion of most of the orders diversity. The Lamiales branching ships of the genera Craterostigma, Lindernia and its allies, hith- above the Plocospermataceae and Oleaceae are called ªcore erto classified within the Scrophulariaceae, were analyzed. Se- Lamialesº in the following text. The most recent classification quences of the chloroplast trnK intron and the matK gene by the Angiosperm Phylogeny Group (APG2, 2003) recognizes (~ 2.5 kb) were generated for representatives of all major line- 20 families. -
Evo-Devo and the Search for Homology
Available online at www.sciencedirect.com SCIENCE @DIRECT Theory in Bi0sciences ELSEVIER Theory in Biosciences 124 (2005) 213-241 www.elsevier.de/thbio Evo-devo and the search for homology ("sameness") in biological systems Rolf Rutishauser*, Philip Moline Institut fffr Systematische Botanik der Universitdt Zffrich, Zollikerstr. 107, CH-8008 Zffrich, Switzerland Received 14 May 2005; accepted 8 September 2005 Abstract Developmental biology and evolutionary studies have merged into evolutionary develop- mental biology ("evo-devo"). This synthesis already influenced and still continues to change the conceptual framework of structural biology. One of the cornerstones of structural biology is the concept of homology. But the search for homology ("sameness") of biological structures depends on our favourite perspectives (axioms, paradigms). Five levels of homology ("sameness") can be identified in the literature, although they overlap to some degree: (i) serial homology (homonomy) within modular organisms, (ii) historical homology (synapo- morphy), which is taken as the only acceptable homology by many biologists, (iii) underlying homology (i.e., parallelism) in closely related taxa, (iv) deep evolutionary homology due to the "same" master genes in distantly related phyla, and (v) molecular homology exclusively at gene level. The following essay gives emphasis on the heuristic advantages of seemingly opposing perspectives in structural biology, with examples mainly from comparative plant morphology. The organization of the plant body in the majority of angiosperms led to the recognition of the classical root-shoot model. In some lineages bauplan rules were transcended during evolution and development. This resulted in morphological misfits such as the Podostemaceae, peculiar eudicots adapted to submerged river rocks. -
Molecular Phylogenetic Analysis of Podostemaceae: Implications for Taxonomy of Major Groups
bs_bs_banner Botanical Journal of the Linnean Society, 2012, 169, 461–492. With 2 figures Molecular phylogenetic analysis of Podostemaceae: implications for taxonomy of major groups SATOSHI KOI1*, YOKO KITA2, YUMIKO HIRAYAMA1, ROLF RUTISHAUSER3, KONRAD A. HUBER3 and MASAHIRO KATO1 1Department of Botany, National Museum of Nature and Science, Tsukuba 305-0005, Japan 2Department of Biological Sciences, University of Tokyo, Hongo, Tokyo 113-0033, Japan 3Institute for Systematic Botany, University of Zurich, CH-8008 Zurich, Switzerland Received 23 August 2011; revised 15 January 2012; accepted for publication 27 March 2012 The river-weed family Podostemaceae (c. 300 species in c. 54 genera) shows a number of morphological innovations to be adapted to its unusual aquatic habitat, and its unique or rare bauplan features have been reflected in the traditional (i.e. non-molecular) classification recognizing numerous monotypic or oligospecific genera. The infra- subfamilial relationships of many genera remained unclear. The present study used molecular phylogenetic analysis of matK sequences for 657 samples (c. 132 species/c. 43 genera). The family was traditionally divided into three subfamilies (Podostemoideae, Tristichoideae and Weddellinoideae). American Podostemoideae were shown to be polyphyletic and divided into four clades, i.e. Ceratolacis, Diamantina, Podostemum and all other genera. Among the podostemoid clades, Diamantina was the first branching clade and a clade comprising Mourera and the Apinagia subclade was then sister to the remainder of the New World and Old World Podostemoideae with low statistic supports. The Old World Podostemoideae comprised four monophyletic clades, i.e. two African clades, one Madagascan clade and one Asian clade, although the relationships among these clades and American Ceratolacis and Podostemum were poorly resolved. -
A Phylogenetic Approach
20 Tulane Undergraduate Research Journal | 2015 Floral Character Evolution in Response to an Aquatic Environment in Podostemaceae: A Phylogenetic Approach Rachel Herschlag, Tulane University Abstract Habitat transition is a common driving force for change in morphological characters. One of the most dramatic habitat transitions is that between terrestrial and aquatic ecosystems, which has occurred numerous times in both directions throughout the evolutionary history of flowering plants. Podostemaceae, more commonly known as the riverweeds, evolved from terrestrial to freshwater ecosystems and subsequently experienced an overall reduction in number of floral characters. Taking a phylogenetic approach, this study served as a preliminary investigation into evolutionary trends of four floral characters: 1) stamen number, 2) tepal number, 3) stigma number and 4) locule number. Mapped on a phylogeny based upon Maximum Likelihood, all four characters show overall reduction but characters became reduced at different rates. Stamen and tepal numbers showed a rapid initial decrease followed by a gradual increase, stigma number showed a rapid initial decrease then stabilization, and locule number showed a gradual persistent decrease. The difference in trends among the four floral characters is likely due to differences in habitat, but further research is needed. It may seem surprising that organisms so well adapted Podostemaceae, commonly known as the riverweed to survive and reproduce in their environments evolve family, are the largest strictly aquatic flowering plant into new habitats, yet habitat transitions have occurred family (approximately 280 species, 49 genera) and numerous times throughout the history of life. one of the best examples of reduced morphological Transitions into new habitats are often accompanied by features associated with colonization into aquatic changes in species morphology, as natural selection acts habitats (Cook and Rutishauser, 2007). -
Phylogeny of Lamiidae Reveals Increased Resolution and Support for Internal Relationships That Have Remained Elusive
American Journal of Botany 101(2): 287–299. 2014. P HYLOGENY OF LAMIIDAE 1 N ANCY F . R EFULIO-RODRIGUEZ 2 AND R ICHARD G. OLMSTEAD 2,3 2 Department of Biology, Box 355325, University of Washington, Seattle, Washington 98195 USA • Premise of the study: The Lamiidae, a clade composed of approximately 15% of all fl owering plants, consists of fi ve orders: Boraginales, Gentianales, Garryales, Lamiales, and Solanales; and four families unplaced in an order: Icacinaceae, Metteniusi- aceae, Oncothecaceae, and Vahliaceae. Our understanding of the phylogenetic relationships of Lamiidae has improved signifi - cantly in recent years, however, relationships among the orders and unplaced families of the clade remain partly unresolved. Here, we present a phylogenetic analysis of the Lamiidae based on an expanded sampling, including all families together, for the fi rst time, in a single phylogenetic analyses. • Methods: Phylogenetic analyses were conducted using maximum parsimony, maximum likelihood, and Bayesian approaches. Analyses included nine plastid regions ( atpB , matK , ndhF , psbBTNH , rbcL , rps4 , rps16 , trnL - F , and trnV - atpE ) and the mitochondrial rps3 region, and 129 samples representing all orders and unplaced families of Lamiidae. • Key results: Maximum Likelihood (ML) and Bayesian trees provide good support for Boraginales sister to Lamiales, with successive outgroups (Solanales + Vahlia) and Gentianales, together comprising the core Lamiidae. Early branching patterns are less well supported, with Garryales only poorly supported as sister to the above ‘core’ and a weakly supported clade composed of Icacinaceae, Metteniusaceae, and Oncothecaceae sister to all other Lamiidae. • Conclusions: Our phylogeny of Lamiidae reveals increased resolution and support for internal relationships that have remained elusive. -
Free-Sample-Pages.Pdf
Published by Plant Gateway Ltd., Hertford, SG13 7BX, United Kingdom © Plant Gateway 2014 This book is in copyright. Subject to statutory exception and to the provision of relevant col- lective licensing agreements, no reproduction of any part may take place without the written permission of Plant Gateway Ltd. ISBN 978-0-9929993-0-8 eISBN 978-0-9929993-1-5 Plant Gateway Ltd. has no responsibility for the persistence or accuracy of URLS for external or third-party internet websites referred to in this book, and does not guarantee that any content on such websites is, or will remain, accurate or appropriate. Additional information on the book can be found at: www.plantgateway.com An appropriate citation for this eBook is: Byng JW. 2014. The Flowering Plants Handbook: A practical guide to families and genera of the world. Plant Gateway Ltd., Hertford, UK. eBook available from: www.plantgateway.com From the war of nature, from famine and death, the most exalted object which we are capable of conceiving, namely, the production of the higher animals, directly follows. There is grandeur in this view of life, with its several powers, having been originally breathed into a few forms or into one; and that, whilst this planet has gone cycling on according to the fixed law of gravity, from so simple a beginning endless forms most beautiful and most wonderful have been, and are being, evolved. Charles Darwin On The Origin of Species (1859) CONTENTS The Flowering Plants Handbook A practical guide to families and genera of the world James W. Byng eBook version CONTENTS DEDICATION This work is a dwarf standing on the shoulders of giants and is dedicated to the many botanists, both past and present, for the huge body of knowledge that exists today. -
Succulent Plants
This guide covers the main succulent species, other than cacti, Sajeva Maurizio and Groves , Madeleine Catherine Rutherford Plants Succulent regulated by the Convention on International Trade in Endangered Succulent Plants Species (CITES). It provides information on the implementation of the Convention for these species with details on their A guide to CITES-listed species distribution, uses, traded parts and derivatives, and scientific names. It is written for the non-expert and additional sections cover identification, guidance on CITES documentation and key resources. ISBN 9781999896201 Catherine Rutherford Madeleine Groves 7819999 896201 Maurizio Sajeva Succulent Plants A guide to CITES-listed species Catherine Rutherford Madeleine Groves Maurizio Sajeva © Rutherford Groves Publishing, London 2018 The authors have asserted their rights to be identified as the authors of this work in accordance with the Copyright, Designs and Patents Act 1988. All rights reserved. No part of this publication may be reproduced, stored in a retrieval system, or transmitted, in any form, or by any means, electronic, mechanical, photocopying, recording or otherwise, without written permission of the publisher unless in accordance with the provisions of the Copyright Designs and Patents Act 1988. Great care has been taken to maintain the accuracy of the information contained in this work. However, neither the publisher, the editors nor the authors can be held responsible for any consequences arising from use of the information contained herein. First published in 2018 by Rutherford Groves Publishing London, UK ISBN 978-1-9998962-0-1 Design and page layout: Trockenbrot Published with the support of the Swedish Environmental Protection Agency Printed in the UK by Blissetts The paper used for this publication is FSC certified Contents Introduction ..................................... -
Reconstructing Deep‐Time Palaeoclimate Legacies in The
Received: 25 October 2016 | Revised: 23 December 2017 | Accepted: 4 January 2018 DOI: 10.1111/geb.12724 RESEARCH PAPER Reconstructing deep-time palaeoclimate legacies in the clusioid Malpighiales unveils their role in the evolution and extinction of the boreotropical flora Andrea S. Meseguer1,2,3 | Jorge M. Lobo4 | Josselin Cornuault1 | David Beerling5 | Brad R. Ruhfel6,7 | Charles C. Davis7 | Emmanuelle Jousselin2 | Isabel Sanmartín1 1Department of Biodiversity and Conservation, Real Jardín Botanico, Abstract RJB-CSIC, Madrid, Spain Aim: During its entire history, the Earth has gone through periods of climate change similar in scale 2 INRA, UMR 1062 CBGP (INRA, IRD, and pace to the warming trend observed today in the Anthropocene. The impact of these ancient CIRAD, Montpellier SupAgro), The Center for Biology and Management of Populations climatic events on the evolutionary trajectories of organisms provides clues on the organismal (CBGP), Montferrier-sur-Lez, France response to climate change, including extinction, migration and persistence. Here, we examine the 3CNRS, UMR 5554 Institut des Sciences de evolutionary response to climate cooling/warming events of the clusioid families Calophyllaceae, l’Evolution (Universite de Montpellier), Podostemaceae and Hypericaceae (CPH clade) and the genus Hypericum as test cases. Montpellier, France 4Department of Biogeography and Global Location: Holarctic. Change, Museo Nacional Ciencias Naturales, Time period: Late Cretaceous–Cenozoic. MNCN-CSIC, Madrid, Spain 5Department of Animal and Plant Sciences, Major taxa studied: Angiosperms. University of Sheffield, Sheffield, United Kingdom Methods: We use palaeoclimate simulations, species distribution models and phylogenetic com- 6Department of Biological Sciences, Eastern parative approaches calibrated with fossils. Kentucky University, Richmond, Kentucky Results: Ancestral CPH lineages could have been distributed in the Holarctic 100 Ma, occupying 7 Department of Organismic and tropical subhumid assemblages, a finding supported by the fossil record. -
Alternative Approaches for Resolving the Phylogeny of Lamiaceae
OUT OF THE BUSHES AND INTO THE TREES: ALTERNATIVE APPROACHES FOR RESOLVING THE PHYLOGENY OF LAMIACEAE By GRANT THOMAS GODDEN A DISSERTATION PRESENTED TO THE GRADUATE SCHOOL OF THE UNIVERSITY OF FLORIDA IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY UNIVERSITY OF FLORIDA 2014 © 2014 Grant Thomas Godden To my father, Clesson Dale Godden Jr., who would have been proud to see me complete this journey, and to Mr. Tea and Skippyjon Jones, who sat patiently by my side and offered friendship along the way ACKNOWLEDGMENTS I would like to express my deepest gratitude for the consistent support of my advisor, Dr. Pamela Soltis, whose generous allocation of time, innovative advice, encouragement, and mentorship positively shaped my research and professional development. I also offer my thanks to Dr. J. Gordon Burleigh, Dr. Bryan Drew, Dr. Ingrid Jordon-Thaden, Dr. Stephen Smith, and the members of my committee—Dr. Nicoletta Cellinese, Dr. Walter Judd, Dr. Matias Kirst, and Dr. Douglas Soltis—for their helpful advice, guidance, and research support. I also acknowledge the many individuals who helped make possible my field research activities in the United States and abroad. I wish to extend a special thank you to Dr. Angelica Cibrian Jaramillo, who kindly hosted me in her laboratory at the National Laboratory of Genomics for Biodiversity (Langebio) and helped me acquire collecting permits and resources in Mexico. Additional thanks belong to Francisco Mancilla Barboza, Gerardo Balandran, and Praxaedis (Adan) Sinaca for their field assistance in Northeastern Mexico; my collecting trip was a great success thanks to your resourcefulness and on-site support. -
Podostemaceae)
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Phyton, Annales Rei Botanicae, Horn Jahr/Year: 2007 Band/Volume: 47_1_2 Autor(en)/Author(s): Grob Valentin, Pfeifer Evelin, Rutishauser Rolf Artikel/Article: Morphology, Development and Regeneration of Thelethylax minutiflora, a Madagascar River-weed (Podostemaceae). 205-229 ©Verlag Ferdinand Berger & Söhne Ges.m.b.H., Horn, Austria, download unter www.biologiezentrum.at Phyton (Horn, Austria) Vol. 47 Fasc. 1-2 205-229 19. 12. 2007 Morphology, Development and Regeneration of Thelethylax minutiflora, a Madagascan River-weed (Podostemaceae) By Valentin GROB, Evelin PFEIFER and Rolf RUTISHAUSER*) With 34 Figures Received November 14, 2007 Keywords: Podostemaceae, Thelethylax minutiflora. - Anatomy, aquatic plants, character evolution, comparative morphology, dedifferentiation, develop- ment, regeneration, root-ribbons, shoot dimorphism. - Flora of Africa, Madagascar. Summary GROB V., PFEIFER E. & RUTISHAUSER R. 2007. Morphology, development and re- generation of Thelethylax minutiflora, a Madagascan river-weed {Podostemaceae). - Phyton (Horn, Austria) 47(1-2): 205-229, with 34 figures. - English with German summary. Thelethylax (2 species) is one of three podostemoid genera, which are endemic to Madagascar. This paper deals with the structure and development of T. minutiflora. Characters typical for this species include: green ribbon-like roots have exogenous finger-like holdfasts; root tips are covered with prominent dorsiventral caps; shoots arise mainly from endogenous buds along roots; shoots are dimorphic: vegetative shoots have repeatedly forked leaves, reproductive shoots are reduced to 2-4 scales and a terminal flower. Thelethylax also shows endogenous flower formation along old stem portions, due to dedifferentiation of cortex tissue. -
Cactus and Succulent Plants: Status Survey and Conservation Action Plan
Donors to the SSC Conservation Communications Programme and Cactus and Succulent Plants: Status Survey and Conservation Action Plan The IUCN/Species Survival Commission is committed to communicate important species conservation information to natural resource managers, decision-makers and others whose actions affect the conservation of biodiversity. The SSC’s Action Plans, Occasional Papers, news magazine (Species), Membership Directory and other publications are supported by a wide variety of generous donors including: The Sultanate of Oman established the Peter Scott IUCN/SSC Action Plan Fund in 1990. The Fund supports Action Plan development and implementation; to date, more than 80 grants have been made from the Fund to Specialist Groups. As a result, the Action Plan Programme has progressed at an accelerated level and the network has grown and matured significantly. The SSC is grateful to the Sultanate of Oman for its confidence in and support for species conservation worldwide. The Chicago Zoological Society (CZS] provides significant in-kind and cash support to the SSC, including grants for special projects, editorial and design services, staff secondments and related support services. The mission of CZS is to help people develop a sustainable and harmonious relationship with nature. The Zoo carries out its mission by informing and inspiring 2,000,OOO annual visitors, serving as a refuge for species threatened with extinction, developing scientific approaches to manage species successfully in zoos and the wild, and working with other zoos, agencies, and protected areas around the world to conserve habitats and wildlife. The Council ofAgriculture (CO&, Taiwan has awarded major grants to the SSC’s Wildlife Trade Programme and Conservation Communications Programme. -
Brad R. Ruhfel 2,8 , Volker Bittrich 3 , Claudia P. Bove 4 , Mats H. G
American Journal of Botany 98(2): 306–325. 2011. P HYLOGENY OF THE CLUSIOID CLADE (MALPIGHIALES): E VIDENCE FROM THE PLASTID AND MITOCHONDRIAL GENOMES 1 Brad R. Ruhfel 2,8 , Volker Bittrich 3 , Claudia P. Bove 4 , Mats H. G. Gustafsson 5 , C. Thomas Philbrick 6 , Rolf Rutishauser 7 , Zhenxiang Xi 2 , and Charles C. Davis 2,8 2 Department of Organismic and Evolutionary Biology, Harvard University Herbaria, 22 Divinity Avenue, Cambridge, Massachusetts 02138 USA; 3 Rua Dr. M á rio de Nucci, 500, Cidade Universit á ria 13083-290, Campinas, Brazil; 4 Departamento de Bot â nica, Museu Nacional, Universidade Federal do Rio de Janeiro, Quinta da Boa Vista, Rio de Janeiro 20940-040, Brazil; 5 Ecoinformatics and Biodiversity, Department of Biological Sciences, Aarhus University, Ole Worms All é , Building 1137, 8000 Å rhus C, Denmark; 6 Western Connecticut State University, Biological & Environmental Sciences, 181 White Street, Danbury, Connecticut 06810 USA; and 7 University of Zurich, Institute of Systematic Botany, Zollikerstrasse 107, CH-8008 Zurich, Switzerland • Premise of the study : The clusioid clade includes fi ve families (i.e., Bonnetiaceae, Calophyllaceae, Clusiaceae s.s., Hyperi- caceae, and Podostemaceae) represented by 94 genera and ~1900 species. Species in this clade form a conspicuous element of tropical forests worldwide and are important in horticulture, timber production, and pharmacology. We conducted a taxon-rich multigene phylogenetic analysis of the clusioids to clarify phylogenetic relationships in this clade. • Methods : We analyzed plastid ( matK , ndhF , and rbcL ) and mitochondrial (matR ) nucleotide sequence data using parsimony, maximum likelihood, and Bayesian inference. Our combined data set included 194 species representing all major clusioid subclades, plus numerous species spanning the taxonomic, morphological, and biogeographic breadth of the clusioid clade.