P. 1 Cop14 Prop. 24 CONVENTION on INTERNATIONAL TRADE in ENDANGERED SPECIES of WILD FAUNA and FLORA
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What Did the First Cacti Look Like
What Did the First Cactus Look like? An Attempt to Reconcile the Morphological and Molecular Evidence Author(s): M. Patrick Griffith Source: Taxon, Vol. 53, No. 2 (May, 2004), pp. 493-499 Published by: International Association for Plant Taxonomy (IAPT) Stable URL: http://www.jstor.org/stable/4135628 . Accessed: 03/12/2014 10:33 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]. International Association for Plant Taxonomy (IAPT) is collaborating with JSTOR to digitize, preserve and extend access to Taxon. http://www.jstor.org This content downloaded from 192.135.179.249 on Wed, 3 Dec 2014 10:33:44 AM All use subject to JSTOR Terms and Conditions TAXON 53 (2) ' May 2004: 493-499 Griffith * The first cactus What did the first cactus look like? An attempt to reconcile the morpholog- ical and molecular evidence M. Patrick Griffith Rancho Santa Ana Botanic Garden, 1500 N. College Avenue, Claremont, California 91711, U.S.A. michael.patrick. [email protected] THE EXTANT DIVERSITYOF CAC- EARLYHYPOTHESES ON CACTUS TUS FORM EVOLUTION Cacti have fascinated students of naturalhistory for To estimate evolutionaryrelationships many authors many millennia. Evidence exists for use of cacti as food, determinewhich morphological features are primitive or medicine, and ornamentalplants by peoples of the New ancestral versus advanced or derived. -
Copyright Notice
Copyright Notice This electronic reprint is provided by the author(s) to be consulted by fellow scientists. It is not to be used for any purpose other than private study, scholarship, or research. Further reproduction or distribution of this reprint is restricted by copyright laws. If in doubt about fair use of reprints for research purposes, the user should review the copyright notice contained in the original journal from which this electronic reprint was made. Journal of Vegetation Science 7: 667-680, 1996 © IAVS; Opulus Press Uppsala. Printed in Sweden - Biogeographic patterns of Argentine cacti - 667 Species richness of Argentine cacti: A test of biogeographic hypotheses Mourelle, Cristina & Ezcurra, Exequiel Centro de Ecología, UNAM, Apartado Postal 70-275, 04510 - Mexico, D.F., Mexico; Fax +52 5 6228995; E-mail [email protected] Abstract. Patterns of species richness are described for 50 cacti and (e) pereskioid cacti. Columnar species have columnar, 109 globose and 50 opuntioid cacti species in 318 column-like stems with ribs, formed by an arrangement grid cells (1°×1°) covering Argentina. Biological richness of the areoles in longitudinal rows. These species have hypotheses were tested by regressing 15 environmental parallel vascular bundles, separated by succulent paren- descriptors against species richness in each group. We also chyma, sometimes fusing towards a woody base in the included the collection effort (estimated as the logarithm of the number of herbarium specimens collected in each cell) to adults. We broadly considered as columnar cacti: estimate the possible error induced by underrepresentation in candelabriform arborescent species, unbranched erect certain cells. -
Pereskia Aculeata Miller and Pereskia Grandifolia Haw) And
325 A publication of CHEMICAL ENGINEERING TRANSACTIONS VOL. 75, 2019 The Italian Association of Chemical Engineering Online at www.cetjournal.it Guest Editors: Sauro Pierucci, Laura Piazza Copyright © 2019, AIDIC Servizi S.r.l. ISBN 978-88-95608-72-3; ISSN 2283-9216 DOI: 10.3303/CET1975055 Centesimal Evaluation of Two Species of Ora-pro-nobis (Pereskia aculeata Miller and Pereskia grandifolia Haw) and Application in Extruded Product a a a b Maria F. F. Carvalho , Leonardo M. M , Maiara P. Mendes , Vanesa Gesser , Claudia C. F. monteirod, Rosane M. Peraltab, Antonio R. G. Monteiroc* a Centre of Agriculture Science, Food Science division. State University of Maringá, 5790, Colombo Av., CEP: 87020-900, Maringá-PR, Brazil. b Biochemistry Department, State University of Maringá, 5790, Colombo Av., CEP: 87020-900, Maringá-PR, Brazil. c Food Engineer Department, State University of Maringá, 5790, Colombo Av., CEP: 87020-900, Maringá-PR, Brazil. d Department of Design, State University of Maringá, 5790, Colombo Av., CEP: 87020-900, Maringá-PR, Brazil. [email protected] Some vegetables that are rarely used and/or unknown in daily menu, can represent great sources of vital nutrients to maintain the metabolic health of their consumers. Among them is Pereskia spp family, commonly known as ora-pro-nobis, "the flesh of the poor". According to RDC No. 54/2012 (BRASIL, 2012), Ora-pro- nobis can be considered a functional food due to its high protein content (approximately 25%), with high digestibility (80%), 3.35g/100g of calcium, 2.42g/100g of potassium, 1.13g/100g of phosphorus, 0.45g/100g of magnesium and 0.98g/100g of sulphur, leaf (140.36 ppm) and stem (88.75 ppm) iron. -
Taxonomy and Distribution of Opuntia and Related Plants
Taxonomy and Distribution of Opuntia and Related Genera Raul Puente Desert Botanical Garden Donald Pinkava Arizona State University Subfamily Opuntioideae Ca. 350 spp. 13-18 genera Very wide distribution (Canada to Patagonia) Morphological consistency Glochids Bony arils Generic Boundaries Britton and Rose, 1919 Anderson, 2001 Hunt, 2006 -- Seven genera -- 15 genera --18 genera Austrocylindropuntia Austrocylindropuntia Grusonia Brasiliopuntia Brasiliopuntia Maihuenia Consolea Consolea Nopalea Cumulopuntia Cumulopuntia Opuntia Cylindropuntia Cylindropuntia Pereskiopsis Grusonia Grusonia Pterocactus Maihueniopsis Corynopuntia Tacinga Miqueliopuntia Micropuntia Opuntia Maihueniopsis Nopalea Miqueliopuntia Pereskiopsis Opuntia Pterocactus Nopalea Quiabentia Pereskiopsis Tacinga Pterocactus Tephrocactus Quiabentia Tunilla Tacinga Tephrocactus Tunilla Classification: Family: Cactaceae Subfamily: Maihuenioideae Pereskioideae Cactoideae Opuntioideae Wallace, 2002 Opuntia Griffith, P. 2002 Nopalea nrITS Consolea Tacinga Brasiliopuntia Tunilla Miqueliopuntia Cylindropuntia Grusonia Opuntioideae Grusonia pulchella Pereskiopsis Austrocylindropuntia Quiabentia 95 Cumulopuntia Tephrocactus Pterocactus Maihueniopsis Cactoideae Maihuenioideae Pereskia aculeata Pereskiodeae Pereskia grandiflora Talinum Portulacaceae Origin and Dispersal Andean Region (Wallace and Dickie, 2002) Cylindropuntia Cylindropuntia tesajo Cylindropuntia thurberi (Engelmann) F. M. Knuth Cylindropuntia cholla (Weber) F. M. Knuth Potential overlapping areas between the Opuntia -
The New York Botanical Garden
Vol. XV DECEMBER, 1914 No. 180 JOURNAL The New York Botanical Garden EDITOR ARLOW BURDETTE STOUT Director of the Laboratories CONTENTS PAGE Index to Volumes I-XV »33 PUBLISHED FOR THE GARDEN AT 41 NORTH QUBKN STRHBT, LANCASTER, PA. THI NEW ERA PRINTING COMPANY OFFICERS 1914 PRESIDENT—W. GILMAN THOMPSON „ „ _ i ANDREW CARNEGIE VICE PRESIDENTS J FRANCIS LYNDE STETSON TREASURER—JAMES A. SCRYMSER SECRETARY—N. L. BRITTON BOARD OF- MANAGERS 1. ELECTED MANAGERS Term expires January, 1915 N. L. BRITTON W. J. MATHESON ANDREW CARNEGIE W GILMAN THOMPSON LEWIS RUTHERFORD MORRIS Term expire January. 1916 THOMAS H. HUBBARD FRANCIS LYNDE STETSON GEORGE W. PERKINS MVLES TIERNEY LOUIS C. TIFFANY Term expire* January, 1917 EDWARD D. ADAMS JAMES A. SCRYMSER ROBERT W. DE FOREST HENRY W. DE FOREST J. P. MORGAN DANIEL GUGGENHEIM 2. EX-OFFICIO MANAGERS THE MAYOR OP THE CITY OF NEW YORK HON. JOHN PURROY MITCHEL THE PRESIDENT OP THE DEPARTMENT OP PUBLIC PARES HON. GEORGE CABOT WARD 3. SCIENTIFIC DIRECTORS PROF. H. H. RUSBY. Chairman EUGENE P. BICKNELL PROF. WILLIAM J. GIES DR. NICHOLAS MURRAY BUTLER PROF. R. A. HARPER THOMAS W. CHURCHILL PROF. JAMES F. KEMP PROF. FREDERIC S. LEE GARDEN STAFF DR. N. L. BRITTON, Director-in-Chief (Development, Administration) DR. W. A. MURRILL, Assistant Director (Administration) DR. JOHN K. SMALL, Head Curator of the Museums (Flowering Plants) DR. P. A. RYDBERG, Curator (Flowering Plants) DR. MARSHALL A. HOWE, Curator (Flowerless Plants) DR. FRED J. SEAVER, Curator (Flowerless Plants) ROBERT S. WILLIAMS, Administrative Assistant PERCY WILSON, Associate Curator DR. FRANCIS W. PENNELL, Associate Curator GEORGE V. -
Crop Ecology, Cultivation and Uses of Cactus Pear
CROP ECOLOGY, CULTIVATION AND USES OF CACTUS PEAR Advance draft prepared for the IX INTERNATIONAL CONGRESS ON CACTUS PEAR AND COCHINEAL CAM crops for a hotter and drier world Coquimbo, Chile, 26-30 March 2017 CROP ECOLOGY, CULTIVATION AND USES OF CACTUS PEAR Editorial team Prof. Paolo Inglese, Università degli Studi di Palermo, Italy; General Coordinator Of the Cactusnet Dr. Candelario Mondragon, INIFAP, Mexico Dr. Ali Nefzaoui, ICARDA, Tunisia Prof. Carmen Sáenz, Universidad de Chile, Chile Coordination team Makiko Taguchi, FAO Harinder Makkar, FAO Mounir Louhaichi, ICARDA Editorial support Ruth Duffy Book design and layout Davide Moretti, Art&Design − Rome Published by the Food and Agriculture Organization of the United Nations and the International Center for Agricultural Research in the Dry Areas Rome, 2017 The designations employed and the FAO encourages the use, reproduction and presentation of material in this information dissemination of material in this information product do not imply the expression of any product. Except where otherwise indicated, opinion whatsoever on the part of the Food material may be copied, downloaded and Agriculture Organization of the United and printed for private study, research Nations (FAO), or of the International Center and teaching purposes, or for use in non- for Agricultural Research in the Dry Areas commercial products or services, provided (ICARDA) concerning the legal or development that appropriate acknowledgement of FAO status of any country, territory, city or area as the source and copyright holder is given or of its authorities, or concerning the and that FAO’s endorsement of users’ views, delimitation of its frontiers or boundaries. -
The Wonderful World of Cacti. July 7, 2020
OHIO STATE UNIVERSITY EXTENSION Succulents part 1: The wonderful world of cacti. July 7, 2020 Betzy Rivera. Master Gardener Volunteer OSU Extension – Franklin County OHIO STATE UNIVERSITY EXTENSION Succulent plants Are plants with parts that are thickened and fleshy, capacity that helps to retain water in arid climates. Over 25 families have species of succulents. The most representative families are: Crassulaceae, Agavaceae, Aizoaceae, Euphorbiacea and Cactaceae. 2 OHIO STATE UNIVERSITY EXTENSION The Cactaceae family is endemic to America and the distribution extends throughout the continent from Canada to Argentina, in addition to the Galapagos Islands and Antilles Most important centers of diversification (Bravo-Hollis & Sánchez-Mejorada, 1978; Hernández & Godínez, 1994; Arias-Montes, 1993; Anderson, 2001; Guzmán et al., 2003; Ortega- Baes & Godínez-Alvarez, 2006 3 OHIO STATE UNIVERSITY EXTENSION There is an exception — one of the 1,800 species occurs naturally in Africa, Sri Lanka, and Madagascar Rhipsalis baccifera 4 OHIO STATE UNIVERSITY EXTENSION The Cactaceae family includes between ~ 1,800 and 2,000 species whose life forms include climbing, epiphytic, shrubby, upright, creeping or decumbent plants, globose, cylindrical or columnar in shape (Bravo-Hollis & Sánchez-Mejorada, 1978; Hernández & Godínez, 1994; Guzmán et al., 2003). 5 OHIO STATE UNIVERSITY EXTENSION Cacti are found in a wide variety of environments, however the greatest diversity of forms is found in arid and semi-arid areas, where they play an important role in maintaining the stability of ecosystems (Bravo-Hollis & Sánchez-Mejorada, 1978; Hernández & Godínez, 1994; Guzmán et al., 2003). 6 OHIO STATE UNIVERSITY EXTENSION The Cactaceae family are dicotyledonous plants 2 cotyledons Astrophytum myriostigma (common names: Bishop´s cap cactus, bishop’s hat or miter cactus) 7 OHIO STATE UNIVERSITY EXTENSION General Anatomy of a Cactus Cactus spines are produced from specialized structures called areoles, a kind of highly reduced branch. -
L'intégration Du Genre Leuenbergeria Lodé Dans Sa Propre Sous-Famille : Leuenbergerioideae Mayta & Mol
L'intégration du genre Leuenbergeria Lodé dans sa propre sous-famille : Leuenbergerioideae Mayta & Mol. Nov., 2021/09/30 11:03 1/4 subfam. nov. L'intégration du genre Leuenbergeria Lodé dans sa propre sous-famille : Leuenbergerioideae Mayta & Mol. Nov., subfam. nov. par Luis Mayta 1) et EA Molinari-Novoa 2) Cet article a été initialement publié dans Succulentopi@ n°12 p.6-7, le 3 janvier 2015. Pendant longtemps (Butterworth & Wallace, 2005 ; Edwards et al., 2005 ; Butterworth & Edwards, 2008 ; Bárcenas et al., 2011), a été reconnue la paraphylie 3) de Pereskia Mill., l’un des genres les plus primitifs des cactées (Edwards & Donoghue, 2006). Actuellement, les Pereskiae «véritables» ont été délimitées par Nyffeler & Eggli (2010). Stevens (2014) propose dans son APWeb le nom Rhodocactus (A. Berger) F.M. Knuth (in Backeberg & Knuth, 1935) comme une alternative possible pour les espèces qui en sont exclues (également connues collectivement comme “clade du Nord”, qui est plus ancien que tout autre dans les cactées, cf. Arakaki et al., 2011). Ce nom a été établi originalement comme un sous-genre de Pereskia. Cependant, cette alternative n'est pas acceptable, car Berger (1926, 1929) a choisi un “véritable” Pereskia comme type de ce sous-genre, et de ce fait, il s’agit d’un synonyme (Backeberg, 1958 ; Leuenberg 1986, 2007). Lodé (2013) a reconnu cette situation et a transféré toutes les espèces concernées dans son nouveau genre, Leuenbergeria, mais ce changement qui était correct, a été ignoré par la plupart des cactologistes, qui maintiennent la paraphylie de Pereskia et donc, la paraphylie de toute la sous-famille. -
Gooseberry Flyer.Pub
ST PE T Barbados Gooseberry ER Please Call AL 553-5236 Photo by ARC-PPRI. Photographs by TNC Hawaii What is it? Why is it a What is MoMISC What can you do? • Barbados gooseberry problem in doing? • Do not grow Barbados (Pereskia aculeata) is gooseberry. Hawaii? • The Molokai/Maui a cactus from the West Invasive Species • If left unchecked, Indies that is invading Committee is a multi- • Learn to identify invasive Barbados gooseberry Hawaii. sector partnership species in the MoMISC can form a dense fighting to protect brochure. canopy that quickly • Gooseberry appears Molokai from invasive smothers out native as an erect woody plants and animals that • Call MoMISC at 553-5236 vegetation under a liana when young, and threaten our if you see Barbados solid blanket of later a thorny vine that environment, economy, gooseberry anywhere on vines. can climb up trees. and quality of life. Molokai. • It forms dense, spiny • The 2-4 inch long, eye- • MoMISC prevents new • Grow native plants thickets and litter shaped leaves are a invasive species from instead of non-native which are miserable dark glossy green. becoming established on plants. Encourage your for hikers and Molokai through friends to do the same. hunters. • It is covered in clusters education and outreach. of long slender spines • Before purchasing a (1-2 inches long). • Plants can spread • MoMISC works with the plant, check if it is through seeds or community to control invasive. You can ask • The flowers are white, various plant parts invasive species on your nursery, call yellowish or pinkish. (leaves, stems, etc). -
CACTACEAE 1. PERESKIA Miller, Gard. Dict. Abr., Ed. 4. 1754
CACTACEAE 仙人掌科 xian ren zhang ke Li Zhenyu (李振宇)1; Nigel P. Taylor2 Fleshy perennials, shrubs, trees or vines, terrestrial or epiphytic. Stems jointed, terete, globose, flattened, or fluted, mostly leafless and variously spiny. Leaves alternate, flat or subulate to terete, vestigial, or entirely absent; spines, glochids (easily detached, small, bristlelike spines), and flowers always arising from cushionlike, axillary areoles (modified short shoots). Flowers solitary, sessile, rarely clustered and stalked (in Pereskia), bisexual, rarely unisexual, actinomorphic or occasionally zygomorphic. Receptacle tube (hypanthium or perianth tube) absent or short to elongate, naked or invested with leaflike bracts, scales, areoles, and hairs, bristles, or spines; perianth segments usually numerous, in a sepaloid to petaloid series. Stamens numerous, variously inserted in throat and tube; anthers 2-loculed, dehiscing longitudinally. Ovary (pericarpel) inferior, rarely superior, 1-loculed, with 3 to many parietal (rarely basal) placentas; ovules usually numerous; style 1; stigmas 2 to numerous, papillate, rarely 2-fid. Fruit juicy or dry, naked, scaly, hairy, bristly, or spiny, indehiscent or dehiscent, when juicy then pulp derived from often deliquescent funicles (except in Pereskia). Seeds usually numerous, often arillate or strophiolate; embryo curved or rarely straight; endosperm present or absent; cotyledons reduced or vestigial, rarely leaflike. About 110 genera and more than 1000 species: temperate and tropical America; Rhipsalis baccifera (J. S. Mueller) Stearn native in tropical Africa, Madagascar, Comoros, Mascarenes, and Sri Lanka; some species of other genera now extensively naturalized in the Old World through human agency; more than 60 genera and 600 species cultivated as ornamentals or hedges in China, of which four genera and seven species more or less naturalized. -
Perennial Edible Fruits of the Tropics: an and Taxonomists Throughout the World Who Have Left Inventory
United States Department of Agriculture Perennial Edible Fruits Agricultural Research Service of the Tropics Agriculture Handbook No. 642 An Inventory t Abstract Acknowledgments Martin, Franklin W., Carl W. Cannpbell, Ruth M. Puberté. We owe first thanks to the botanists, horticulturists 1987 Perennial Edible Fruits of the Tropics: An and taxonomists throughout the world who have left Inventory. U.S. Department of Agriculture, written records of the fruits they encountered. Agriculture Handbook No. 642, 252 p., illus. Second, we thank Richard A. Hamilton, who read and The edible fruits of the Tropics are nnany in number, criticized the major part of the manuscript. His help varied in form, and irregular in distribution. They can be was invaluable. categorized as major or minor. Only about 300 Tropical fruits can be considered great. These are outstanding We also thank the many individuals who read, criti- in one or more of the following: Size, beauty, flavor, and cized, or contributed to various parts of the book. In nutritional value. In contrast are the more than 3,000 alphabetical order, they are Susan Abraham (Indian fruits that can be considered minor, limited severely by fruits), Herbert Barrett (citrus fruits), Jose Calzada one or more defects, such as very small size, poor taste Benza (fruits of Peru), Clarkson (South African fruits), or appeal, limited adaptability, or limited distribution. William 0. Cooper (citrus fruits), Derek Cormack The major fruits are not all well known. Some excellent (arrangements for review in Africa), Milton de Albu- fruits which rival the commercialized greatest are still querque (Brazilian fruits), Enriquito D. -
Rethinking Phylogenetics Using Caryophyllales (Angiosperms), Matk Gene and Trnk Intron As Experimental Platform
Rethinking phylogenetics using Caryophyllales (angiosperms), matK gene and trnK intron as experimental platform Sunny Sheliese Crawley Dissertation submitted to the faculty of the Virginia Polytechnic Institute and State University in partial fulfillment of the requirements for the degree of Doctor of Philosophy In Biological Sciences Khidir W. Hilu Eric P. Beers Carla V. Finkielstein Jill C. Sible December 2, 2011 Blacksburg, Virginia Keywords: (phylogeny, missing data, caryophyllids, trnK intron, matK, RNA editing, gnetophytes) Copyright 2011, Sunny Sheliese Crawley Rethinking phylogenetics using Caryophyllales (angiosperms), matK gene and trnK intron as experimental platform Sunny Sheliese Crawley ABSTRACT The recent call to reconstruct a detailed picture of the tree of life for all organisms has forever changed the field of molecular phylogenetics. Sequencing technology has improved to the point that scientists can now routinely sequence complete plastid/mitochondrial genomes and thus, vast amounts of data can be used to reconstruct phylogenies. These data are accumulating in DNA sequence repositories, such as GenBank, where everyone can benefit from the vast growth of information. The trend of generating genomic-region rich datasets has far outpaced the expasion of datasets by sampling a broader array of taxa. We show here that expanding a dataset both by increasing genomic regions and species sampled using GenBank data, despite the inherent missing DNA that comes with GenBank data, can provide a robust phylogeny for the plant order Caryophyllales (angiosperms). We also investigate the utility of trnK intron in phylogeny reconstruction at relativley deep evolutionary history (the caryophyllid order) by comparing it with rapidly evolving matK. We show that trnK intron is comparable to matK in terms of the proportion of variable sites, parsimony informative sites, the distribution of those sites among rate classes, and phylogenetic informativness across the history of the order.