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Guide to the Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- LILIACEAE
Guide to the Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- LILIACEAE LILIACEAE de Jussieu 1789 (Lily Family) (also see AGAVACEAE, ALLIACEAE, ALSTROEMERIACEAE, AMARYLLIDACEAE, ASPARAGACEAE, COLCHICACEAE, HEMEROCALLIDACEAE, HOSTACEAE, HYACINTHACEAE, HYPOXIDACEAE, MELANTHIACEAE, NARTHECIACEAE, RUSCACEAE, SMILACACEAE, THEMIDACEAE, TOFIELDIACEAE) As here interpreted narrowly, the Liliaceae constitutes about 11 genera and 550 species, of the Northern Hemisphere. There has been much recent investigation and re-interpretation of evidence regarding the upper-level taxonomy of the Liliales, with strong suggestions that the broad Liliaceae recognized by Cronquist (1981) is artificial and polyphyletic. Cronquist (1993) himself concurs, at least to a degree: "we still await a comprehensive reorganization of the lilies into several families more comparable to other recognized families of angiosperms." Dahlgren & Clifford (1982) and Dahlgren, Clifford, & Yeo (1985) synthesized an early phase in the modern revolution of monocot taxonomy. Since then, additional research, especially molecular (Duvall et al. 1993, Chase et al. 1993, Bogler & Simpson 1995, and many others), has strongly validated the general lines (and many details) of Dahlgren's arrangement. The most recent synthesis (Kubitzki 1998a) is followed as the basis for familial and generic taxonomy of the lilies and their relatives (see summary below). References: Angiosperm Phylogeny Group (1998, 2003); Tamura in Kubitzki (1998a). Our “liliaceous” genera (members of orders placed in the Lilianae) are therefore divided as shown below, largely following Kubitzki (1998a) and some more recent molecular analyses. ALISMATALES TOFIELDIACEAE: Pleea, Tofieldia. LILIALES ALSTROEMERIACEAE: Alstroemeria COLCHICACEAE: Colchicum, Uvularia. LILIACEAE: Clintonia, Erythronium, Lilium, Medeola, Prosartes, Streptopus, Tricyrtis, Tulipa. MELANTHIACEAE: Amianthium, Anticlea, Chamaelirium, Helonias, Melanthium, Schoenocaulon, Stenanthium, Veratrum, Toxicoscordion, Trillium, Xerophyllum, Zigadenus. -
Coreopsideae Daniel J
Chapter42 Coreopsideae Daniel J. Crawford, Mes! n Tadesse, Mark E. Mort, "ebecca T. Kimball and Christopher P. "andle HISTORICAL OVERVIEW AND PHYLOGENY In a cladistic analysis of morphological features of Heliantheae by Karis (1993), Coreopsidinae were reported Morphological data to be an ingroup within Heliantheae s.l. The group was A synthesis and analysis of the systematic information on represented in the analysis by Isostigma, Chrysanthellum, tribe Heliantheae was provided by Stuessy (1977a) with Cosmos, and Coreopsis. In a subsequent paper (Karis and indications of “three main evolutionary lines” within "yding 1994), the treatment of Coreopsidinae was the the tribe. He recognized ! fteen subtribes and, of these, same as the one provided above except for the follow- Coreopsidinae along with Fitchiinae, are considered ing: Diodontium, which was placed in synonymy with as constituting the third and smallest natural grouping Glossocardia by "obinson (1981), was reinstated following within the tribe. Coreopsidinae, including 31 genera, the work of Veldkamp and Kre# er (1991), who also rele- were divided into seven informal groups. Turner and gated Glossogyne and Guerreroia as synonyms of Glossocardia, Powell (1977), in the same work, proposed the new tribe but raised Glossogyne sect. Trionicinia to generic rank; Coreopsideae Turner & Powell but did not describe it. Eryngiophyllum was placed as a synonym of Chrysanthellum Their basis for the new tribe appears to be ! nding a suit- following the work of Turner (1988); Fitchia, which was able place for subtribe Jaumeinae. They suggested that the placed in Fitchiinae by "obinson (1981), was returned previously recognized genera of Jaumeinae ( Jaumea and to Coreopsidinae; Guardiola was left as an unassigned Venegasia) could be related to Coreopsidinae or to some Heliantheae; Guizotia and Staurochlamys were placed in members of Senecioneae. -
Outline of Angiosperm Phylogeny
Outline of angiosperm phylogeny: orders, families, and representative genera with emphasis on Oregon native plants Priscilla Spears December 2013 The following listing gives an introduction to the phylogenetic classification of the flowering plants that has emerged in recent decades, and which is based on nucleic acid sequences as well as morphological and developmental data. This listing emphasizes temperate families of the Northern Hemisphere and is meant as an overview with examples of Oregon native plants. It includes many exotic genera that are grown in Oregon as ornamentals plus other plants of interest worldwide. The genera that are Oregon natives are printed in a blue font. Genera that are exotics are shown in black, however genera in blue may also contain non-native species. Names separated by a slash are alternatives or else the nomenclature is in flux. When several genera have the same common name, the names are separated by commas. The order of the family names is from the linear listing of families in the APG III report. For further information, see the references on the last page. Basal Angiosperms (ANITA grade) Amborellales Amborellaceae, sole family, the earliest branch of flowering plants, a shrub native to New Caledonia – Amborella Nymphaeales Hydatellaceae – aquatics from Australasia, previously classified as a grass Cabombaceae (water shield – Brasenia, fanwort – Cabomba) Nymphaeaceae (water lilies – Nymphaea; pond lilies – Nuphar) Austrobaileyales Schisandraceae (wild sarsaparilla, star vine – Schisandra; Japanese -
ASTERACEAE José Ángel Villarreal-Quintanilla* José Luis Villaseñor-Ríos** Rosalinda Medina-Lemos**
FLORA DEL VALLE DE TEHUACÁN-CUICATLÁN Fascículo 62. ASTERACEAE José Ángel Villarreal-Quintanilla* José Luis Villaseñor-Ríos** Rosalinda Medina-Lemos** *Departamento de Botánica Universidad Autónoma Agraria Antonio Narro **Departamento de Botánica Instituto de Biología, UNAM INSTITUTO DE BIOLOGÍA UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO 2008 Primera edición: octubre de 2008 D.R. © Universidad Nacional Autónoma de México Instituto de Biología. Departamento de Botánica ISBN 968-36-3108-8 Flora del Valle de Tehuacán-Cuicatlán ISBN 970-32-5084-4 Fascículo 62 Dirección de los autores: Departamento de Botánica Universidad Autónoma Agraria Antonio Narro Buenavista, Saltillo C.P. 25315 Coahuila, México Universidad Nacional Autónoma de México Instituto de Biología. Departamento de Botánica. 3er. Circuito de Ciudad Universitaria Coyoacán, 04510. México, D.F. 1 En la portada: 2 1. Mitrocereus fulviceps (cardón) 2. Beaucarnea purpusii (soyate) 3 4 3. Agave peacockii (maguey fibroso) 4. Agave stricta (gallinita) Dibujo de Elvia Esparza FLORA DEL VALLE DE TEHUACÁN-CUICATLÁN 62: 1-59. 2008 ASTERACEAE1 Bercht. & J.Presl Tribu Tageteae José Ángel Villarreal-Quintanilla José Luis Villaseñor-Ríos Rosalinda Medina-Lemos Bibliografía. Bremer, K. 1994. Asteraceae. Cladistics & Classification. Timber Press. Portland, Oregon. 752 p. McVaugh, R. 1984. Compositae. In: W.R. Anderson (ed.). Flora Novo-Galiciana. Ann Arbor The University of Michi- gan Press 12: 40-42. Panero, J.L. & V.A. Funk. 2002. Toward a phylogene- tic subfamily classification for the Compositae (Asteraceae). Proc. Biol. Soc. Washington 115: 909-922. Villaseñor Ríos, J.L. 1993. La familia Asteraceae en México. Rev. Soc. Mex. Hist. Nat. 44: 117-124. Villaseñor Ríos, J.L. 2003. Diversidad y distribución de las Magnoliophyta de México. -
The Flora of Guadalupe Island, Mexico
qQ 11 C17X NH THE FLORA OF GUADALUPE ISLAND, MEXICO By Reid Moran Published by the California Academy of Sciences San Francisco, California Memoirs of the California Academy of Sciences, Number 19 The pride of Guadalupe Island, the endemic Cisfuiillw giiailulupensis. flowering on a small islet off the southwest coast, with cliffs of the main island as a background; 19 April 1957. This plant is rare on the main island, surviving only on cliffs out of reach of goats, but common here on sjoatless Islote Nccro. THE FLORA OF GUADALUPE ISLAND, MEXICO Q ^ THE FLORA OF GUADALUPE ISLAND, MEXICO By Reid Moran y Published by the California Academy of Sciences San Francisco, California Memoirs of the California Academy of Sciences, Number 19 San Francisco July 26, 1996 SCIENTIFIC PUBLICATIONS COMMITTEE: Alan E. Lcviton. Ediinr Katie Martin, Managing Editor Thomas F. Daniel Michael Ghiselin Robert C. Diewes Wojciech .1. Pulawski Adam Schift" Gary C. Williams © 1906 by the California Academy of Sciences, Golden (iate Park. San Francisco, California 94118 All rights reserved. No part of this publication may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopying, recording, or any infcMination storage or retrieval system, without permission in writing from the publisher. Library of Congress Catalog Card Number: 96-084362 ISBN 0-940228-40-8 TABLE OF CONTENTS Abstract vii Resumen viii Introduction 1 Guadalupe Island Description I Place names 9 Climate 13 History 15 Other Biota 15 The Vascular Plants Native -
Chromosome Numbers in Compositae, XII: Heliantheae
SMITHSONIAN CONTRIBUTIONS TO BOTANY 0 NCTMBER 52 Chromosome Numbers in Compositae, XII: Heliantheae Harold Robinson, A. Michael Powell, Robert M. King, andJames F. Weedin SMITHSONIAN INSTITUTION PRESS City of Washington 1981 ABSTRACT Robinson, Harold, A. Michael Powell, Robert M. King, and James F. Weedin. Chromosome Numbers in Compositae, XII: Heliantheae. Smithsonian Contri- butions to Botany, number 52, 28 pages, 3 tables, 1981.-Chromosome reports are provided for 145 populations, including first reports for 33 species and three genera, Garcilassa, Riencourtia, and Helianthopsis. Chromosome numbers are arranged according to Robinson’s recently broadened concept of the Heliantheae, with citations for 212 of the ca. 265 genera and 32 of the 35 subtribes. Diverse elements, including the Ambrosieae, typical Heliantheae, most Helenieae, the Tegeteae, and genera such as Arnica from the Senecioneae, are seen to share a specialized cytological history involving polyploid ancestry. The authors disagree with one another regarding the point at which such polyploidy occurred and on whether subtribes lacking higher numbers, such as the Galinsoginae, share the polyploid ancestry. Numerous examples of aneuploid decrease, secondary polyploidy, and some secondary aneuploid decreases are cited. The Marshalliinae are considered remote from other subtribes and close to the Inuleae. Evidence from related tribes favors an ultimate base of X = 10 for the Heliantheae and at least the subfamily As teroideae. OFFICIALPUBLICATION DATE is handstamped in a limited number of initial copies and is recorded in the Institution’s annual report, Smithsonian Year. SERIESCOVER DESIGN: Leaf clearing from the katsura tree Cercidiphyllumjaponicum Siebold and Zuccarini. Library of Congress Cataloging in Publication Data Main entry under title: Chromosome numbers in Compositae, XII. -
Rinconada Checklist-02Jun19
Checklist1 of Vascular Flora of Rinconada Mine and Rinconada Trail San Luis Obispo County, California (2 June 2019) David J. Keil Robert F. Hoover Herbarium Biological Sciences Department California Polytechnic State University San Luis Obispo, California Scientific Name Common Name Family Rare n ❀ Achyrachaena mollis blow wives ASTERACEAE o n ❀ Acmispon americanus var. americanus Spanish-clover FABACEAE o n Acmispon brachycarpus shortpod deervetch FABACEAE v n ❀ Acmispon glaber var. glaber common deerweed FABACEAE o n Acmispon parviflorus miniature deervetch FABACEAE o n ❀ Acmispon strigosus strigose deer-vetch FABACEAE o 1 Please notify the author of additions or corrections to this list ([email protected]). ❀ — See Wildflowers of San Luis Obispo, California, second edition (2018) for photograph. Most are illustrated in the first edition as well; old names for some species in square brackets. n — California native i — exotic species, introduced to California, naturalized or waif. v — documented by one or more specimens (Consortium of California Herbaria record; specimen in OBI; or collection that has not yet been accessioned) o — observed during field surveys; no voucher specimen known Rare—California Rare Plant Rank Scientific Name Common Name Family Rare n Acmispon wrangelianus California deervetch FABACEAE v n ❀ Acourtia microcephala sacapelote ASTERACEAE o n ❀ Adelinia grandis Pacific hound's tongue BORAGINACEAE v n ❀ Adenostoma fasciculatum var. chamise ROSACEAE o fasciculatum n Adiantum jordanii California maidenhair fern PTERIDACEAE o n Agastache urticifolia nettle-leaved horsemint LAMIACEAE v n ❀ Agoseris grandiflora var. grandiflora large-flowered mountain-dandelion ASTERACEAE v n Agoseris heterophylla var. cryptopleura annual mountain-dandelion ASTERACEAE v n Agoseris heterophylla var. heterophylla annual mountain-dandelion ASTERACEAE o i Aira caryophyllea silver hairgrass POACEAE o n Allium fimbriatum var. -
Ndhf Sequence Evolution and the Major Clades in the Sunflower Family KI-JOONG KIM* and ROBERT K
Proc. Natl. Acad. Sci. USA Vol. 92, pp. 10379-10383, October 1995 Evolution ndhF sequence evolution and the major clades in the sunflower family KI-JOONG KIM* AND ROBERT K. JANSENt Department of Botany, University of Texas, Austin, TX 78713-7640 Communicated by Peter H. Raven, Missouri Botanical Garden, St. Louis, MO, June 21, 1995 ABSTRACT An extensive sequence comparison of the either too short or too conserved to provide adequate numbers chloroplast ndhF gene from all major clades of the largest of characters in recently evolved families. A number of alter- flowering plant family (Asteraceae) shows that this gene native genes have been suggested as potential candidates for provides -3 times more phylogenetic information than rbcL. phylogenetic comparisons at lower taxonomic levels (9). The This is because it is substantially longer and evolves twice as phylogenetic utility of one of these, matK, has been recently fast. The 5' region (1380 bp) ofndhF is very different from the demonstrated (10). Comparison of sequences of two chloro- 3' region (855 bp) and is similar to rbcL in both the rate and plast genomes (rice and tobacco), however, revealed only two the pattern of sequence change. The 3' region is more A+T- genes, rpoCl and ndhF, that are considerably longer and evolve rich, has higher levels of nonsynonymous base substitution, faster than rbcL (9, 11). We selected ndhF because it is longer and shows greater transversion bias at all codon positions. and evolves slightly faster than rpoCl (11), because rpoCl has These differences probably reflect different functional con- an intron that may require additional effort in DNA amplifi- straints on the 5' and 3' regions of nduhF. -
GENOME EVOLUTION in MONOCOTS a Dissertation
GENOME EVOLUTION IN MONOCOTS A Dissertation Presented to The Faculty of the Graduate School At the University of Missouri In Partial Fulfillment Of the Requirements for the Degree Doctor of Philosophy By Kate L. Hertweck Dr. J. Chris Pires, Dissertation Advisor JULY 2011 The undersigned, appointed by the dean of the Graduate School, have examined the dissertation entitled GENOME EVOLUTION IN MONOCOTS Presented by Kate L. Hertweck A candidate for the degree of Doctor of Philosophy And hereby certify that, in their opinion, it is worthy of acceptance. Dr. J. Chris Pires Dr. Lori Eggert Dr. Candace Galen Dr. Rose‐Marie Muzika ACKNOWLEDGEMENTS I am indebted to many people for their assistance during the course of my graduate education. I would not have derived such a keen understanding of the learning process without the tutelage of Dr. Sandi Abell. Members of the Pires lab provided prolific support in improving lab techniques, computational analysis, greenhouse maintenance, and writing support. Team Monocot, including Dr. Mike Kinney, Dr. Roxi Steele, and Erica Wheeler were particularly helpful, but other lab members working on Brassicaceae (Dr. Zhiyong Xiong, Dr. Maqsood Rehman, Pat Edger, Tatiana Arias, Dustin Mayfield) all provided vital support as well. I am also grateful for the support of a high school student, Cady Anderson, and an undergraduate, Tori Docktor, for their assistance in laboratory procedures. Many people, scientist and otherwise, helped with field collections: Dr. Travis Columbus, Hester Bell, Doug and Judy McGoon, Julie Ketner, Katy Klymus, and William Alexander. Many thanks to Barb Sonderman for taking care of my greenhouse collection of many odd plants brought back from the field. -
ASHY DOGWEED (Thymophylla [=Dyssodia] Tephroleuca)
ASHY DOGWEED (Thymophylla [=Dyssodia] tephroleuca) 5-Year Review: Summary and Evaluation Photograph: Chris Best, USFWS U.S. Fish and Wildlife Service Corpus Christi Ecological Services Field Office Corpus Christi, Texas September 2011 1 FIVE YEAR REVIEW Ashy dogweed/Thymophylla tephroleuca Blake 1.0 GENERAL INFORMATION 1.1 Reviewers Lead Regional Office: Southwest Regional Office, Region 2 Susan Jacobsen, Chief, Threatened and Endangered Species, 505-248-6641 Wendy Brown, Endangered Species Recovery Coordinator, 505-248-6664 Julie McIntyre, Recovery Biologist, 505-248-6507 Lead Field Office: Corpus Christi Ecological Services Field Office Robyn Cobb, Fish and Wildlife Biologist, 361- 994-9005, ext. 241 Amber Miller, Fish and Wildlife Biologist, 361-994-9005, ext. 247 Cooperating Field Office: Austin Ecological Services Field Office Chris Best, Texas State Botanist, 512- 490-0057, ext. 225 1.2 Purpose of 5-Year Reviews: The U.S. Fish and Wildlife Service (Service or USFWS) is required by section 4(c)(2) of the Endangered Species Act (Act) to conduct a status review of each listed species once every five years. The purpose of a 5-year review is to evaluate whether or not the species’ status has changed since it was listed (or since the most recent 5-year review). Based on the 5-year review, we recommend whether the species should be removed from the list of endangered and threatened species, be changed in status from endangered to threatened, or be changed in status from threatened to endangered. Our original listing as endangered or threatened is based on the species’ status considering the five threat factors described in section 4(a)(1) of the Act. -
Dichelostemma Capitatum Alph. Wood Subsp. Capitatum, BLUE DICKS
Dichelostemma capitatum Alph. Wood subsp. capitatum, BLUE DICKS. Perennial herb, geophytic, corm-bearing, fibrous-rooted, rosetted with 1−3 leaves, acaulous, 1−several- stemmed at base, scabose, 25–100+ cm tall; shoots with only basal leaves, 1 leaf per peduncle (scape), with leaves arched-spreading or laying on ground to ascending through branches of protective shrub, glabrous, slightly glaucous; corm covered with 1−5 fibrous, brown layers, spheroid to top-shaped, 4−16 mm diameter, whitish beneath splitting layers, cormlet fusiform to narrowly ovoid, sessile or on short stolon (< 10 mm long). Stems (peduncles): cylindric, 2−4 mm diameter, white belowground and green turning purplish near ground level. Leaves: alternate, simple with sheath; sheath closed, belowground, white; blade long-linear becoming as long as scape but dying from tip backward, 3.5–20 mm wide, dark green, keeled with a thickened, angular midrib, folded upward from midrib, minutely serrate with backward-pointing teeth on margins, initially long-tapered at tip, parallel-veined, slightly glaucous. Inflorescence: umbel-like, terminal on peduncle, dense and headlike, 15−37 mm across, 6−19(–30+)-flowered, of mixed bud sizes with several flowers opening each day, bracteate, glabrous; peduncle ascending, cylindric, to 1000 mm long, green turning purple to pale lavender near inflorescence, tough due to presence of a cylinder of fiber cells beneath green tissue; bractlet subtending each pedicel; involucre of 4−5 helically alternate bractlets of the outermost flowers, at least -
Cibulnaté a Hlíznaté Rostliny
Cibulnaté a hlíznaté rostliny Přehled druhů 2: Asparagales Řád Asparagales rozsáhlý řád, 14 čeledí, některé obrovské semena rostlin obsahují černé barvivo melanin (některé druhy ho druhotně ztratily) Hosta PREZENTACE © JN Iridaceae (kosatcovité) Řád Asparagales Čeleď Iridaceae (kosatcovité) vytrvalé byliny s oddenky, hlízami, nebo cibulemi stonek přímý nevětvený, někdy zkrácený listy mečovité nebo čárkovité, dvouřadé se souběžnou žilnatinou květy jednotlivé nebo v chudých květenstvích (vějířek nebo srpek) – významné druhy okrasného zahradnictví subtropy až mírné pásmo 70/1750, ČR 3/12 PREZENTACE © JN Iridaceae (kosatcovité) Řád Asparagales Čeleď Iridaceae (kosatcovité) Zahradnicky významné jsou: mečíky (Gladiolus), frézie (Freesia), kosatce (Iris), šafrány (Crocus) Mezi další zahradnicky významné Iridaceae patří např. Crocosmia, Ixia, Tigridia © Saxifraga-Dirk Hilbers © Saxifraga-Inigo Sanchez Iris xiphium http://www.freenatureimages.eu/Plants/Flora%20D-I/Iris%20xiphium/slides/Iris%20xiphium%201,%20Saxifraga-Dirk%20Hilbers.jpg http://www.freenatureimages.eu/Plants/Flora%20D-I/Iris%20xiphium/slides/Iris%20xiphium%202,%20Saxifraga-Inigo%20Sanchez.jpg Iridaceae (kosatcovité) Iris (kosatec) zahrnuje i množství druhů které se neřadí mezi cibuloviny. Do cibulovin patří kosatce sekce Xiphium a Reticulata Sekce Xiphium - původní druhy pocházejí ze středomoří, hlavně Pyrenejí, zde rostou v 1500 m na mořem Cibule se 3-5 masitými šupinami, žlábkovité listy , stvol s 2-3 tuhými zelenými listeny a 2-3 květy, jsou modré se žlutým středem na vnějších okvětních lístcích, v přírodě kvetou koncem června Křížením původních druh této sekce hlavně Iris xiphium a I. tingitana vzniklo velké množství kutivarů – označované jako Dutch iris (holandské kosatce), pěstují se tržně v mnoha barvách (od bílé, žluté, modré až po fialovou) a prodávají jako řezané květiny např.