Phylocode: a Phylogenetic Code of Biological Nomenclature Version 2B
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Dieter Thomas Tietze Editor How They Arise, Modify and Vanish
Fascinating Life Sciences Dieter Thomas Tietze Editor Bird Species How They Arise, Modify and Vanish Fascinating Life Sciences This interdisciplinary series brings together the most essential and captivating topics in the life sciences. They range from the plant sciences to zoology, from the microbiome to macrobiome, and from basic biology to biotechnology. The series not only highlights fascinating research; it also discusses major challenges associated with the life sciences and related disciplines and outlines future research directions. Individual volumes provide in-depth information, are richly illustrated with photographs, illustrations, and maps, and feature suggestions for further reading or glossaries where appropriate. Interested researchers in all areas of the life sciences, as well as biology enthusiasts, will find the series’ interdisciplinary focus and highly readable volumes especially appealing. More information about this series at http://www.springer.com/series/15408 Dieter Thomas Tietze Editor Bird Species How They Arise, Modify and Vanish Editor Dieter Thomas Tietze Natural History Museum Basel Basel, Switzerland ISSN 2509-6745 ISSN 2509-6753 (electronic) Fascinating Life Sciences ISBN 978-3-319-91688-0 ISBN 978-3-319-91689-7 (eBook) https://doi.org/10.1007/978-3-319-91689-7 Library of Congress Control Number: 2018948152 © The Editor(s) (if applicable) and The Author(s) 2018. This book is an open access publication. Open Access This book is licensed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license and indicate if changes were made. -
Species Names in Phylogenetic Nomenclature
Syst. Biol. 48(4):790–807, 1999 Species Names in Phylogenetic Nomenclature PHILIP D. CANTINO,1* HAROLD N. BRYANT,2 KEVIN DE QUEIROZ,3 MICHAEL J. DONOGHUE,4 TORSTEN ERIKSSON,5 DAVID M. HILLIS,6 AND MICHAEL S. Y. LEE7 1Department of Environmental and Plant Biology, Ohio University, Athens, Ohio 45701, USA; E-mail: [email protected] 2Royal Saskatchewan Museum, 2340 Albert Street, Regina, Saskatchewan S4P 3V7, Canada; E-mail: [email protected] 3Department of Vertebrate Zoology, National Museum of Natural History, Smithsonian Institution, Washington, DC 20560, USA; E-mail: [email protected] 4Harvard University Herbaria, 22 Divinity Ave., Cambridge, Massachusetts 02138, USA; E-mail: [email protected] 5Bergius Foundation, Royal Swedish Academy of Sciences, Box 50017, 104 05 Stockholm, Sweden; E-mail: [email protected] 6Section of Integrative Biology, School of Biological Sciences, University of Texas, Austin, Texas 78712, USA; E-mail: [email protected] 7Department of Zoology, University of Queensland, Brisbane, Queensland 4072, Australia; E-mail: [email protected] Abstract.—Linnaean binomial nomenclature is logically incompatible with the phylogenetic nomenclature of de Queiroz and Gauthier (1992, Annu. Rev. Ecol. Syst. 23:449–480): The former is based on the concept of genus, thus making this rank mandatory, while the latter is based on phylo- genetic definitions and requires the abandonment of mandatory ranks. Thus, if species are to re- ceive names under phylogenetic nomenclature, a different method must be devised to name them. Here, 13 methods for naming species in the context of phylogenetic nomenclature are contrasted with each other and with Linnaean binomials. -
Towards Resolving Lamiales Relationships
Schäferhoff et al. BMC Evolutionary Biology 2010, 10:352 http://www.biomedcentral.com/1471-2148/10/352 RESEARCH ARTICLE Open Access Towards resolving Lamiales relationships: insights from rapidly evolving chloroplast sequences Bastian Schäferhoff1*, Andreas Fleischmann2, Eberhard Fischer3, Dirk C Albach4, Thomas Borsch5, Günther Heubl2, Kai F Müller1 Abstract Background: In the large angiosperm order Lamiales, a diverse array of highly specialized life strategies such as carnivory, parasitism, epiphytism, and desiccation tolerance occur, and some lineages possess drastically accelerated DNA substitutional rates or miniaturized genomes. However, understanding the evolution of these phenomena in the order, and clarifying borders of and relationships among lamialean families, has been hindered by largely unresolved trees in the past. Results: Our analysis of the rapidly evolving trnK/matK, trnL-F and rps16 chloroplast regions enabled us to infer more precise phylogenetic hypotheses for the Lamiales. Relationships among the nine first-branching families in the Lamiales tree are now resolved with very strong support. Subsequent to Plocospermataceae, a clade consisting of Carlemanniaceae plus Oleaceae branches, followed by Tetrachondraceae and a newly inferred clade composed of Gesneriaceae plus Calceolariaceae, which is also supported by morphological characters. Plantaginaceae (incl. Gratioleae) and Scrophulariaceae are well separated in the backbone grade; Lamiaceae and Verbenaceae appear in distant clades, while the recently described Linderniaceae are confirmed to be monophyletic and in an isolated position. Conclusions: Confidence about deep nodes of the Lamiales tree is an important step towards understanding the evolutionary diversification of a major clade of flowering plants. The degree of resolution obtained here now provides a first opportunity to discuss the evolution of morphological and biochemical traits in Lamiales. -
Ornamental Garden Plants of the Guianas, Part 3
; Fig. 170. Solandra longiflora (Solanaceae). 7. Solanum Linnaeus Annual or perennial, armed or unarmed herbs, shrubs, vines or trees. Leaves alternate, simple or compound, sessile or petiolate. Inflorescence an axillary, extra-axillary or terminal raceme, cyme, corymb or panicle. Flowers regular, or sometimes irregular; calyx (4-) 5 (-10)- toothed; corolla rotate, 5 (-6)-lobed. Stamens 5, exserted; anthers united over the style, dehiscing by 2 apical pores. Fruit a 2-celled berry; seeds numerous, reniform. Key to Species 1. Trees or shrubs; stems armed with spines; leaves simple or lobed, not pinnately compound; inflorescence a raceme 1. S. macranthum 1. Vines; stems unarmed; leaves pinnately compound; inflorescence a panicle 2. S. seaforthianum 1. Solanum macranthum Dunal, Solanorum Generumque Affinium Synopsis 43 (1816). AARDAPPELBOOM (Surinam); POTATO TREE. Shrub or tree to 9 m; stems and leaves spiny, pubescent. Leaves simple, toothed or up to 10-lobed, to 40 cm. Inflorescence a 7- to 12-flowered raceme. Corolla 5- or 6-lobed, bluish-purple, to 6.3 cm wide. Range: Brazil. Grown as an ornamental in Surinam (Ostendorf, 1962). 2. Solanum seaforthianum Andrews, Botanists Repository 8(104): t.504 (1808). POTATO CREEPER. Vine to 6 m, with petiole-tendrils; stems and leaves unarmed, glabrous. Leaves pinnately compound with 3-9 leaflets, to 20 cm. Inflorescence a many- flowered panicle. Corolla 5-lobed, blue, purple or pinkish, to 5 cm wide. Range:South America. Grown as an ornamental in Surinam (Ostendorf, 1962). Sterculiaceae Monoecious, dioecious or polygamous trees and shrubs. Leaves alternate, simple to palmately compound, petiolate. Inflorescence an axillary panicle, raceme, cyme or thyrse. -
Phylocode: a Phylogenetic Code of Biological Nomenclature
PhyloCode: A Phylogenetic Code of Biological Nomenclature Philip D. Cantino and Kevin de Queiroz (equal contributors; names listed alphabetically) Advisory Group: William S. Alverson, David A. Baum, Harold N. Bryant, David C. Cannatella, Peter R. Crane, Michael J. Donoghue, Torsten Eriksson*, Jacques Gauthier, Kenneth Halanych, David S. Hibbett, David M. Hillis, Kathleen A. Kron, Michael S. Y. Lee, Alessandro Minelli, Richard G. Olmstead, Fredrik Pleijel*, J. Mark Porter, Heidi E. Robeck, Greg W. Rouse, Timothy Rowe*, Christoffer Schander, Per Sundberg, Mikael Thollesson, and Andre R. Wyss. *Chaired a committee that authored a portion of the current draft. Most recent revision: April 8, 2000 1 Table of Contents Preface Preamble Division I. Principles Division II. Rules Chapter I. Taxa Article 1. The Nature of Taxa Article 2. Clades Article 3. Hierarchy and Rank Chapter II. Publication Article 4. Publication Requirements Article 5. Publication Date Chapter III. Names Section 1. Status Article 6 Section 2. Establishment Article 7. General Requirements Article 8. Registration Chapter IV. Clade Names Article 9. General Requirements for Establishment of Clade Names Article 10. Selection of Clade Names for Establishment Article 11. Specifiers and Qualifying Clauses Chapter V. Selection of Accepted Names Article 12. Precedence Article 13. Homonymy Article 14. Synonymy Article 15. Conservation Chapter VI. Provisions for Hybrids Article 16. Chapter VII. Orthography Article 17. Orthographic Requirements for Establishment Article 18. Subsequent Use and Correction of Established Names Chapter VIII. Authorship of Names Article 19. Chapter IX. Citation of Authors and Registration Numbers Article 20. Chapter X. Governance Article 21. Glossary Table 1. Equivalence of Nomenclatural Terms Appendix A. -
BIOLOGICAL SYSTEMATICS and EVOLUTIONARY THEORY By
BIOLOGICAL SYSTEMATICS AND EVOLUTIONARY THEORY by Aleta Quinn BA, University of Maryland, 2005 BS, University of Maryland, 2005 Submitted to the Graduate Faculty of The Kenneth P. Dietrich School of Arts and Sciences in partial fulfillment of the requirements for the degree of Doctor of Philosophy University of Pittsburgh 2015 UNIVERSITY OF PITTSBURGH KENNETH P. DIETRICH SCHOOL OF ARTS AND SCIENCES This dissertation was presented by Aleta Quinn It was defended on July 1, 2015 and approved by James Lennox, PhD, History & Philosophy of Science Sandra Mitchell, PhD, History & Philosophy of Science Kenneth Schaffner, PhD, History & Philosophy of Science Jeffrey Schwartz, PhD, Anthropology Dissertation Director: James Lennox, PhD, History & Philosophy of Science ii Copyright © by Aleta Quinn 2015 iii BIOLOGICAL SYSTEMATICS AND EVOLUTIONARY THEORY Aleta Quinn, PhD University of Pittsburgh, 2015 In this dissertation I examine the role of evolutionary theory in systematics (the science that discovers biodiversity). Following Darwin’s revolution, systematists have aimed to reconstruct the past. My dissertation analyzes common but mistaken assumptions about sciences that reconstruct the past by tracing the assumptions to J.S. Mill. Drawing on Mill’s contemporary, William Whewell, I critique Mill’s assumptions and develop an alternative and more complete account of systematic inference as inference to the best explanation. First, I analyze the inadequate view: that scientists use causal theories to hypothesize what past chains of events must have been, and then form hypotheses that identify segments of a network of events and causal transactions between events. This model assumes that scientists can identify events in the world by reference to neatly delineated properties, and that discovering causal laws is simply a matter of testing what regularities hold between events so delineated. -
1992 New Zealand Botanical Society President: Dr Eric Godley Secretary/Treasurer: Anthony Wright
NEW ZEALAND BOTANICAL SOCIETY NEWSLETTER NUMBER 28 JUNE 1992 New Zealand Botanical Society President: Dr Eric Godley Secretary/Treasurer: Anthony Wright Committee: Sarah Beadel, Ewen Cameron, Colin Webb, Carol West Address: New Zealand Botanical Society C/- Auckland Institute & Museum Private Bag 92018 AUCKLAND Subscriptions The 1992 ordinary and institutional subs are $14 (reduced to $10 if paid by the due date on the subscription invoice). The 1992 student sub, available to full-time students, is $7 (reduced to $5 if paid by the due date on the subscription invoice). Back issues of the Newsletter are available at $2.50 each - from Number 1 (August 1985) to Number 28 (June 1992). Since 1986 the Newsletter has appeared quarterly in March, June, September and December. New subscriptions are always welcome and these, together with back issue orders, should be sent to the Secretary/Treasurer (address above). Subscriptions are due by 28 February of each year for that calendar year. Existing subscribers are sent an invoice with the December Newsletter for the next year's subscription which offers a reduction if this is paid by the due date. If you are in arrears with your subscription a reminder notice comes attached to each issue of the Newsletter. Deadline for next issue The deadline for the September 1992 issue (Number 29) is 28 August 1992. Please forward contributions to: Ewen Cameron, Editor NZ Botanical Society Newsletter C/- Auckland Institute & Museum Private Bag 92018 AUCKLAND Cover illustration Mawhai (Sicyos australis) in the Cucurbitaceae. Drawn by Joanna Liddiard from a fresh vegetative specimen from Mangere, Auckland; flowering material from Cuvier Island herbarium specimen (AK 153760) and the close-up of the spine from West Island, Three Kings Islands herbarium specimen (AK 162592). -
Phylogenetic Analyses of Rates of Body Size Evolution Should Show
SSStttooonnnyyy BBBrrrooooookkk UUUnnniiivvveeerrrsssiiitttyyy The official electronic file of this thesis or dissertation is maintained by the University Libraries on behalf of The Graduate School at Stony Brook University. ©©© AAAllllll RRRiiiggghhhtttsss RRReeessseeerrrvvveeeddd bbbyyy AAAuuuttthhhooorrr... The origins of diversity in frog communities: phylogeny, morphology, performance, and dispersal A Dissertation Presented by Daniel Steven Moen to The Graduate School in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy in Ecology and Evolution Stony Brook University August 2012 Stony Brook University The Graduate School Daniel Steven Moen We, the dissertation committee for the above candidate for the Doctor of Philosophy degree, hereby recommend acceptance of this dissertation. John J. Wiens – Dissertation Advisor Associate Professor, Ecology and Evolution Douglas J. Futuyma – Chairperson of Defense Distinguished Professor, Ecology and Evolution Stephan B. Munch – Ecology & Evolution Graduate Program Faculty Adjunct Associate Professor, Marine Sciences Research Center Duncan J. Irschick – Outside Committee Member Professor, Biology Department University of Massachusetts at Amherst This dissertation is accepted by the Graduate School Charles Taber Interim Dean of the Graduate School ii Abstract of the Dissertation The origins of diversity in frog communities: phylogeny, morphology, performance, and dispersal by Daniel Steven Moen Doctor of Philosophy in Ecology and Evolution Stony Brook University 2012 In this dissertation, I combine phylogenetics, comparative methods, and studies of morphology and ecological performance to understand the evolutionary and biogeographical factors that lead to the community structure we see today in frogs. In Chapter 1, I first summarize the conceptual background of the entire dissertation. In Chapter 2, I address the historical processes influencing body-size evolution in treefrogs by studying body-size diversification within Caribbean treefrogs (Hylidae: Osteopilus ). -
Tetrachondraceae Carlos Durán-Espinosa
ISSN 0187-425X Flora de Veracruz Tetrachondraceae Carlos Durán-Espinosa Fascículo Instituto de Ecología, A.C., Xalapa, Ver. Centro de Investigaciones Tropicales 140 2 0 0 6 CONSEJO EDITORIAL Gonzalo Castillo-Campos EDITOR EN JEFE Miguel Cházaro Adolfo Espejo-Serna María Teresa Mejía-Saulés Antonio Lott Michael Nee Jerzy Rzedowski Victoria Sosa Arturo Gómez-Pompa Lorin I. Nevling ASESORES DEL COMITÉ EDITORIAL Manuel Escamilla PRODUCCION EDITORIAL Flora de Veracruz es un proyecto conjunto del Instituto de Ecología, A.C., Xalapa, Veracruz y el Centro de Investigaciones Tropicales. Flora of Veracruz is a collaborative project between the Instituto de Ecología, A. C. and the Centro de Investigaciones Tropicales. D.R. © Arturo Gómez-Pompa Flora de Veracruz Impreso y hecho en México ISSN 0187-425X ISBN 970-709-061-8 Flora de Veracruz es una publicación irregular, octubre 2006. Editor Responsable: Gonzalo Castillo-Campos. No. de Certificado de Reserva otorgado por el Instituto Nacional del Derecho de Autor: 04-2004-071919273100-102. Número de Certificado de Licitud de Título: 13456. Número de certificado de Licitudde Contenido: 11029. Domicilio de la publicación: km 2.5 carretera antigua a Coatepec No. 351, Congregación El Haya, C.P. 91070, Xalapa,Veracruz, México. Imprenta: Editorial Cromo Color S.A. de C.V. Miravalle No.703, Portales, C.P. 03570 México, D.F. Distribuidor: Instituto de Ecología, A.C. km2.5 carretera antigua a Coatepec No. 351, Congregación El Haya, C.P. 91070 Flora de Veracruz Publicada por el Instituto de Ecología A. C. Xalapa, Veracruz, México Fascículo 140 Octubre 2006 TETRACHONDRACEAE Carlos Durán-Espinosa Instituto de Ecología, A.C. -
The Vascular Flora of the Red Hills Forever Wild Tract, Monroe County, Alabama
The Vascular Flora of the Red Hills Forever Wild Tract, Monroe County, Alabama T. Wayne Barger1* and Brian D. Holt1 1Alabama State Lands Division, Natural Heritage Section, Department of Conservation and Natural Resources, Montgomery, AL 36130 *Correspondence: wayne [email protected] Abstract provides public lands for recreational use along with con- servation of vital habitat. Since its inception, the Forever The Red Hills Forever Wild Tract (RHFWT) is a 1785 ha Wild Program, managed by the Alabama Department of property that was acquired in two purchases by the State of Conservation and Natural Resources (AL-DCNR), has pur- Alabama Forever Wild Program in February and Septem- chased approximately 97 500 ha (241 000 acres) of land for ber 2010. The RHFWT is characterized by undulating general recreation, nature preserves, additions to wildlife terrain with steep slopes, loblolly pine plantations, and management areas and state parks. For each Forever Wild mixed hardwood floodplain forests. The property lies tract purchased, a management plan providing guidelines 125 km southwest of Montgomery, AL and is managed by and recommendations for the tract must be in place within the Alabama Department of Conservation and Natural a year of acquisition. The 1785 ha (4412 acre) Red Hills Resources with an emphasis on recreational use and habi- Forever Wild Tract (RHFWT) was acquired in two sepa- tat management. An intensive floristic study of this area rate purchases in February and September 2010, in part was conducted from January 2011 through June 2015. A to provide protected habitat for the federally listed Red total of 533 taxa (527 species) from 323 genera and 120 Hills Salamander (Phaeognathus hubrichti Highton). -
Lamiales – Synoptical Classification Vers
Lamiales – Synoptical classification vers. 2.6.2 (in prog.) Updated: 12 April, 2016 A Synoptical Classification of the Lamiales Version 2.6.2 (This is a working document) Compiled by Richard Olmstead With the help of: D. Albach, P. Beardsley, D. Bedigian, B. Bremer, P. Cantino, J. Chau, J. L. Clark, B. Drew, P. Garnock- Jones, S. Grose (Heydler), R. Harley, H.-D. Ihlenfeldt, B. Li, L. Lohmann, S. Mathews, L. McDade, K. Müller, E. Norman, N. O’Leary, B. Oxelman, J. Reveal, R. Scotland, J. Smith, D. Tank, E. Tripp, S. Wagstaff, E. Wallander, A. Weber, A. Wolfe, A. Wortley, N. Young, M. Zjhra, and many others [estimated 25 families, 1041 genera, and ca. 21,878 species in Lamiales] The goal of this project is to produce a working infraordinal classification of the Lamiales to genus with information on distribution and species richness. All recognized taxa will be clades; adherence to Linnaean ranks is optional. Synonymy is very incomplete (comprehensive synonymy is not a goal of the project, but could be incorporated). Although I anticipate producing a publishable version of this classification at a future date, my near- term goal is to produce a web-accessible version, which will be available to the public and which will be updated regularly through input from systematists familiar with taxa within the Lamiales. For further information on the project and to provide information for future versions, please contact R. Olmstead via email at [email protected], or by regular mail at: Department of Biology, Box 355325, University of Washington, Seattle WA 98195, USA. -
The Species Problem: a Conceptual Problem?
Chapter 2 The Species Problem: A Conceptual Problem? Richard A. Richards Additional information is available at the end of the chapter http://dx.doi.org/10.5772/54134 1. Introduction There have long been multiple ways of conceiving species that divide up biodiversity in dif‐ ferent and inconsistent ways. This “species problem” goes back at least to Aristotle, who used the Greek term eidos (translated as the Latin species) in at least three different ways. [1] Two thousand years later, Darwin confronted the species problem, listing some of the differ‐ ent ways species were conceived. How various are the ideas, that enter into the minds of naturalists when speaking of species. With some, resemblance is the reigning idea & descent goes for little; with others descent is the infallible criterion; with others resemblance goes for almost nothing, & Creation is everything; with other sterility in crossed forms is an unfailing test, whilst with oth‐ ers it is regarded of no value. [2] And one hundred years after Darwin, Ernst Mayr worried about this same problem in a book he edited, titled The Species Problem. Few biological problems have remained as consistently challenging through the past two centuries as the species prob‐ lem. Time after time attempts were made to cut the Gordian knot and declare the species problem solved either by asserting dogmatically that species did not exist or by defining, equally dogmatically, the precise characteristics of spe‐ cies. Alas, these pseudosolutions were obviously unsatisfactory. One might ask: “Why not simply ignore the species © 2013 Richards; licensee InTech. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.