Three New Species of Markea (Solanaceae, Juanulloeae) from Colombia
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Bulletin of Natural History ®
FLORI'IDA MUSEUM BULLETIN OF NATURAL HISTORY ® A MIDDLE EOCENE FOSSIL PLANT ASSEMBLAGE (POWERS CLAY PIT) FROM WESTERN TENNESSEE DavidL. Dilcher and Terry A. Lott Vol. 45, No. 1, pp. 1-43 2005 UNIVERSITY OF FLORIDA GAINESVILLE - The FLORIDA MUSEUM OF NATURAL HiSTORY is Florida«'s state museum of natural history, dedicated to understanding, preser¥ingrand interpreting].biologica[1 diversity and culturafheritage. The BULLETIN OF THE FLORIDA- MUSEUM OF NATURAL HISTORY is a peer-reviewed publication thatpziblishes.the result5 of origifial reseafchin zodlogy, botany, paleontology, and archaeology. Address all inquiries t6 the Managing Editor ofthe Bulletin. Numbers,ofthe Bulletin,afe,published,at itregular intervals. Specific volumes are not'necessarily completed in anyone year. The end of a volume willl·be noted at the foot of the first page ofthe last issue in that volume. Richard Franz, Managing Editor Erika H. Simons, Production BulletinCommittee Richard Franz,,Chairperson Ann Cordell Sarah Fazenbaker Richard Hulbert WilliamMarquardt Susan Milbrath Irvy R. Quitmyer - Scott Robinson, Ex 01#cio Afember ISSN: 0071-6154 Publication Date: October 31,2005 Send communications concerning purchase or exchange of the publication and manustfipt queries to: Managing Editor of the BULLETIN Florida MuseumofNatural-History University offlorida PO Box 117800 Gainesville, FL 32611 -7800 U.S.A. Phone: 352-392-1721 Fax: 352-846-0287 e-mail: [email protected] A MIDDLE EOCENE FOSSIL PLANT ASSEMBLAGE (POWERS CLAY PIT) FROM WESTERN TENNESSEE David L. Dilcher and Terry A. Lottl ABSTRACT Plant megafossils are described, illustrated and discussed from Powers Clay Pit, occurring in the middle Eocene, Claiborne Group of the Mississippi Embayment in western Tennessee. -
Evolutionary Consequences of Dioecy in Angiosperms: the Effects of Breeding System on Speciation and Extinction Rates
EVOLUTIONARY CONSEQUENCES OF DIOECY IN ANGIOSPERMS: THE EFFECTS OF BREEDING SYSTEM ON SPECIATION AND EXTINCTION RATES by JANA C. HEILBUTH B.Sc, Simon Fraser University, 1996 A THESIS SUBMITTED IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY in THE FACULTY OF GRADUATE STUDIES (Department of Zoology) We accept this thesis as conforming to the required standard THE UNIVERSITY OF BRITISH COLUMBIA July 2001 © Jana Heilbuth, 2001 Wednesday, April 25, 2001 UBC Special Collections - Thesis Authorisation Form Page: 1 In presenting this thesis in partial fulfilment of the requirements for an advanced degree at the University of British Columbia, I agree that the Library shall make it freely available for reference and study. I further agree that permission for extensive copying of this thesis for scholarly purposes may be granted by the head of my department or by his or her representatives. It is understood that copying or publication of this thesis for financial gain shall not be allowed without my written permission. The University of British Columbia Vancouver, Canada http://www.library.ubc.ca/spcoll/thesauth.html ABSTRACT Dioecy, the breeding system with male and female function on separate individuals, may affect the ability of a lineage to avoid extinction or speciate. Dioecy is a rare breeding system among the angiosperms (approximately 6% of all flowering plants) while hermaphroditism (having male and female function present within each flower) is predominant. Dioecious angiosperms may be rare because the transitions to dioecy have been recent or because dioecious angiosperms experience decreased diversification rates (speciation minus extinction) compared to plants with other breeding systems. -
A Molecular Phylogeny of the Solanaceae
TAXON 57 (4) • November 2008: 1159–1181 Olmstead & al. • Molecular phylogeny of Solanaceae MOLECULAR PHYLOGENETICS A molecular phylogeny of the Solanaceae Richard G. Olmstead1*, Lynn Bohs2, Hala Abdel Migid1,3, Eugenio Santiago-Valentin1,4, Vicente F. Garcia1,5 & Sarah M. Collier1,6 1 Department of Biology, University of Washington, Seattle, Washington 98195, U.S.A. *olmstead@ u.washington.edu (author for correspondence) 2 Department of Biology, University of Utah, Salt Lake City, Utah 84112, U.S.A. 3 Present address: Botany Department, Faculty of Science, Mansoura University, Mansoura, Egypt 4 Present address: Jardin Botanico de Puerto Rico, Universidad de Puerto Rico, Apartado Postal 364984, San Juan 00936, Puerto Rico 5 Present address: Department of Integrative Biology, 3060 Valley Life Sciences Building, University of California, Berkeley, California 94720, U.S.A. 6 Present address: Department of Plant Breeding and Genetics, Cornell University, Ithaca, New York 14853, U.S.A. A phylogeny of Solanaceae is presented based on the chloroplast DNA regions ndhF and trnLF. With 89 genera and 190 species included, this represents a nearly comprehensive genus-level sampling and provides a framework phylogeny for the entire family that helps integrate many previously-published phylogenetic studies within So- lanaceae. The four genera comprising the family Goetzeaceae and the monotypic families Duckeodendraceae, Nolanaceae, and Sclerophylaceae, often recognized in traditional classifications, are shown to be included in Solanaceae. The current results corroborate previous studies that identify a monophyletic subfamily Solanoideae and the more inclusive “x = 12” clade, which includes Nicotiana and the Australian tribe Anthocercideae. These results also provide greater resolution among lineages within Solanoideae, confirming Jaltomata as sister to Solanum and identifying a clade comprised primarily of tribes Capsiceae (Capsicum and Lycianthes) and Physaleae. -
Solanaceae and Convolvulaceae: Secondary Metabolites Eckart Eich
Solanaceae and Convolvulaceae: Secondary Metabolites Eckart Eich Solanaceae and Convolvulaceae: Secondary Metabolites Biosynthesis, Chemotaxonomy, Biological and Economic Significance (A Handbook) Prof. Dr. Eckart Eich Freie Universität Berlin Institut für Pharmazie - Pharmazeutische Biologie - Königin-Luise-Str. 2 + 4 14195 Berlin Germany E-mail: [email protected] Cover illustration: Flowers of Ipomoea purpurea (L.) Roth [cultivar; Convolvulaceae] (left) and Solandra maxima (Sessé & Mocino) P.S. Green [Solanaceae] (right). Plotted on the photographs are corresponding constituents: the major anthocyanin pigment and the major alkaloid hyoscyamine, respectively. ISBN 978-3-540-74540-2 e-ISBN 978-3-540-74541-9 The Library of Congress Control Number: 2007933490 © 2008 Springer-Verlag Berlin Heidelberg This work is subject to copyright. All rights reserved, whether the whole or part of the material is concerned, specifi cally the rights of translation, reprinting, reuse of illustrations, recitation, broad- casting, reproduction on microfi lm or in any other way, and storage in data banks. Duplication of this publication or parts thereof is permitted only under the provisions of the German Copyright Law of September 9, 1965, in its current version, and permission for use must always be obtained from Springer. Violations are liable for prosecution under the German Copyright Law. The use of registered names, trademarks, etc. in this publication does not imply, even in the absence of a specifi c statement, that such names are exempt from the relevant protective laws and regulations and therefore free for general use. Product liability: The publishers cannot guarantee the accuracy of any information about dosage and application contained in this book. -
Species Selection Maintains Self-Incompatibility E
REPORTS reduction in chemical potential by forming the are already in positions similar to those in the un- 25. The reaction volume was calculated by assuming a ring crystalline phase. In the second scenario, we derlying bulk sapphire. The oxygen collected of triangular cross section. Calculation of the volume yields ~1.7 × 10−20 cm3. Given that the number of assume that oxygen has first adsorbed to the on the LV surface is used to eradicate the facets 22 oxygen atoms per unit volume of a-Al2O3 is 8.63 × 10 LS interface, driven by the reduction in inter- at the outer, top rim of the nanowires once a atoms cm−3, the number of oxygen atoms contained face energy (24, 28), having diffused along the complete (0006) layer is formed. It is this process within the reaction volume is ~1.46 × 103 atoms. The interface from the triple junction. Once oxygen that is the rate-limiting step. number of oxygen atoms needed to deposit a monolayer of close-packed oxygen at the LS (0001) interface was adsorbs, a critical-size nucleus (in the form of calculated by assuming a square and a circular shape a step) forms at the triple junction and sweeps of the interfaces. The area density of a hexagonal close- References and Notes − across the LS (0001) interface, forming a new packed oxygen layer is 1.6 × 1015 atoms cm 2. The 1. E. I. Givargizov, J. Cryst. Growth 31, 20 (1975). a amount of oxygen needed to deposit a monolayer of (0006) layer of -Al2O3 in its wake. -
Filogenia De Markea Rich. (Solanaceae: Juanulloeae) Con Base En Datos De Secuencias De ADN Nuclear Y Del Cloroplasto
Filogenia de Markea Rich. (Solanaceae: Juanulloeae) con base en datos de secuencias de ADN nuclear y del cloroplasto Andrés Orejuela Ramírez Universidad Nacional de Colombia Facultad de Ciencias, Departamento de Biología Bogotá D.C., Colombia Marzo 2016 Filogenia de Markea Rich. (Solanaceae: Juanulloeae) con base en datos de secuencias de ADN nuclear y del cloroplasto Andrés Orejuela Ramírez Tesis presentada como requisito parcial para optar al título de: Magister en Ciencias-Biología Directora: Dra. Clara Inés Orozco Línea de Investigación: Sistemática Universidad Nacional de Colombia Facultad de Ciencias, Departamento de Biología Bogotá D.C., Colombia Marzo 2016 A la memoria de mi padre. A mi madre y mi hijo. Agradecimientos Agradezco muy especialmente a la profesora Clara Inés Orozco por sus enseñanzas, apoyo y constante guía durante todos mis años como estudiante, su paciencia y confianza a pesar de los altibajos me han permitido mejorar cada vez y aprender de errores y problemas. Quiero agradecer a la Universidad Nacional de Colombia y especialmente al Instituto de Ciencias Naturales y a todos sus profesores por el apoyo brindado. A la dirección de investigación, sede Bogotá de la Universidad Nacional (DIB), proyecto 13574, al programa Jóvenes investigadores e innovadores de COLCIENCIAS y al programa de estímulos a la investigación Thomas van der Hammen del Jardín Botánico de Bogotá por la financiación. A los curadores de los herbarios visitados, a las personas que me acompañaron en campo y a quienes facilitaron sus valiosas muestras para los estudios moleculares y fotografías en vivo de las especies que acompañan este documento. Agradezco especialmente a la Dra. -
Logical Species ARG BOL BRA CHI COL ECU GUI PAR PER URU VEN Athenaea Angustifolia (Alm.-Lafetá) I.M.C.Rodrigues & Stehmann E Sciences Athenaea Anonacea Sendtn
MARÍA VIRGINIA PALCHETTI, JUAN JOSÉ CANTERO & GLORIA ESTELA BARBOZA SOUTH AMERICAN SOLANACEAE SUPPLEMENTARY MATERIAL MARÍA VIRGINIA PALCHETTI, JUAN JOSÉ CANTERO & GLORIA Running title: SOUTH Table SI. Checklist of Solanaceae species in South American countries.References. Countries: ARG (Argentina), BOL (Bolivia), BRA (Brazil), CHI (Chile), COL (Colombia), ECU (Ecuador), GUI (Guianas), PAR ESTELA BARBOZA AMERICAN SOLANACEAE (Paraguay), PER (Peru), URU (Uruguay), VEN (Venezuela). Distribution: E (endemic), I (introduced), N (native). 1: introduced species in South America. Academy Section: Biological Species ARG BOL BRA CHI COL ECU GUI PAR PER URU VEN Athenaea angustifolia (Alm.-Lafetá) I.M.C.Rodrigues & Stehmann E Sciences Athenaea anonacea Sendtn. E Athenaea brasiliana Hunz. E e20190017 Athenaea cuspidata Witasek E Athenaea fasciculata (Vell.) I.M.C.Rodrigues & Stehmann N N N N N 92 Athenaea martiana Sendtn. E (2) 92(2) Athenaea picta (Mart.) Sendtn. E Athenaea pogogena (Moric.) Sendtn. E Athenaea sellowiana (Sendtn.) I.M.Rodrigues & Stehmann E Athenaea tomentosa (Sendtn.) I.M.C Rodrigues & Stehmann E Athenaea velutina (Sendtn.) D’Arcy E Athenaea wettsteiniana (Witasek) I.M.C.Rodrigues & Stehmann E Benthamiella azorella (Skottsb.) A.Soriano N N Benthamiella azorelloides Speg. E Benthamiella chubutensis A. Soriano E Benthamiella graminifolia Skottsb. E Benthamiella lanata A. Soriano N N Benthamiella longifolia Speg. E Benthamiella nordenskioldii Dusén ex N.E. Br. N N Benthamiella patagonica Speg. N N Benthamiella pycnophylloides Speg. E Benthamiella skottsbergii A. Soriano E Benthamiella sorianoi S. Arroyo E Benthamiella spegazziniana A. Soriano E Bouchetia anomala (Miers) Britton & Rusby N N N N Browallia abbreviata Benth. E Browallia acutiloba Sagást. & O.D.Carranza N N Browallia albiantha S.Leiva & Tantalean E Browallia americana L. -
Ecology of Plant Hummingbird Interactions in Sachatamia, Ecuador
ECOLOGY OF PLANT HUMMINGBIRD INTERACTIONS IN SACHATAMIA, ECUADOR Tatiana Santander, Esteban Guevara, Francisco Tobar, Holger Beck, Nicole Büttner, Andrea Nieto, Andrés Marcayata, Friederike Richter, María José Gavilanes, Cristian Poveda, Bryan Rojas, Rafael Wüest, Carolina Bello and Catherine H. Graham October 22, 2020 Contents 1. Introduction and project overview 1 2. Methodological Approach 2 Field transects ................................ 2 Timelapse cameras .............................. 5 3. Resulting patterns 5 Planthummingbird interactions ........................ 5 Plants information and phenology ....................... 9 The Network of Interactions .......................... 13 4. Conclusions: 19 Acknowledgements 19 1. Introduction and project overview One of the main hypotheses for how so many related species can cooccur is resource partitioning where species use different resources, which limits competition among species and allows them to coexist. In the case of hummingbirds and plants, each hummingbird species forages on a distinct set of flowers and each flowering plant species is visited by a subset of hummingbirds. Interactions between plants and hummingbirds are mutually beneficial. These mutualistic hummingbirdplant interactions are important from a hummingbird perspective because hummingbirds require nectar to fuel their highenergy lifestyles where they often hover – an energetically costly behavior – to take nectar. From a plant perspective most hummingbirds pollinate flowers as they forage on nectar, though some hummingbirds take nectar from the base of the flower, cheating the flower from this service of pollination. The intricate web of interactions between hummingbirds and their food plants evolved over millennia as a result of diffuse coevolution which yielded a remarkable array of morphological forms and functions. Ongoing human activities, such as deforestation and climate change threaten these interaction webs, yet little is known as to how hummingbirds and their food plants will respond. -
Biodiversity of Food Species of the Solanaceae Family: a Preliminary Taxonomic Inventory of Subfamily Solanoideae
Resources 2015, 4, 277-322; doi:10.3390/resources4020277 OPEN ACCESS resources ISSN 2079-9276 www.mdpi.com/journal/resources Article Biodiversity of Food Species of the Solanaceae Family: A Preliminary Taxonomic Inventory of Subfamily Solanoideae John Samuels Novel Solanaceae Crops Project, Penzance TR20 8XD, UK; E-Mail: [email protected]; Tel.: +44-1736-333773 Academic Editor: Yong-Bi Fu Received: 31 December 2014 / Accepted: 20 April 2015 / Published: 12 May 2015 Abstract: Over the last fifty years there has been a continual reduction in horticultural and agricultural biodiversity of nutritionally important plants, including those of the Solanaceae family. To add to this, the broad range of traditional crops, previously grown on a sustainable scale in some parts of the world, has been replaced by a narrow range of major crops grown as large-scale monocultures. In order to counteract this trend, and to help maintain a broad wealth of genetic resources, conservation is essential. This, in turn, helps to safeguard food security. A taxonomic inventory, covering the diversity of species in a plant group, is an important first step in conservation. The Solanaceae is one of the major plant families providing food species. A survey of the biodiversity, ethnobotany and taxonomy of subfamily Solanoideae was undertaken and is presented here as an inventory of food species. Fifteen genera provide species that are utilised for food across the world. Of these, only four genera contain economically significant cultivated food cropspecies. The majority of these are in the genus Solanum, whilst Capsicum, Physalis and Lycium contribute the remainder of cultivated crop species.