Pilosocereus Robinii) Using New Genetic Tools Tonya D
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Caryophyllales 2018 Instituto De Biología, UNAM September 17-23
Caryophyllales 2018 Instituto de Biología, UNAM September 17-23 LOCAL ORGANIZERS Hilda Flores-Olvera, Salvador Arias and Helga Ochoterena, IBUNAM ORGANIZING COMMITTEE Walter G. Berendsohn and Sabine von Mering, BGBM, Berlin, Germany Patricia Hernández-Ledesma, INECOL-Unidad Pátzcuaro, México Gilberto Ocampo, Universidad Autónoma de Aguascalientes, México Ivonne Sánchez del Pino, CICY, Centro de Investigación Científica de Yucatán, Mérida, Yucatán, México SCIENTIFIC COMMITTEE Thomas Borsch, BGBM, Germany Fernando O. Zuloaga, Instituto de Botánica Darwinion, Argentina Victor Sánchez Cordero, IBUNAM, México Cornelia Klak, Bolus Herbarium, Department of Biological Sciences, University of Cape Town, South Africa Hossein Akhani, Department of Plant Sciences, School of Biology, College of Science, University of Tehran, Iran Alexander P. Sukhorukov, Moscow State University, Russia Michael J. Moore, Oberlin College, USA Compilation: Helga Ochoterena / Graphic Design: Julio C. Montero, Diana Martínez GENERAL PROGRAM . 4 MONDAY Monday’s Program . 7 Monday’s Abstracts . 9 TUESDAY Tuesday ‘s Program . 16 Tuesday’s Abstracts . 19 WEDNESDAY Wednesday’s Program . 32 Wednesday’s Abstracs . 35 POSTERS Posters’ Abstracts . 47 WORKSHOPS Workshop 1 . 61 Workshop 2 . 62 PARTICIPANTS . 63 GENERAL INFORMATION . 66 4 Caryophyllales 2018 Caryophyllales General program Monday 17 Tuesday 18 Wednesday 19 Thursday 20 Friday 21 Saturday 22 Sunday 23 Workshop 1 Workshop 2 9:00-10:00 Key note talks Walter G. Michael J. Moore, Berendsohn, Sabine Ya Yang, Diego F. Registration -
Phylogenetic Analyses of Pilosocereus (Cactaceae) Inferred from Plastid and Nuclear Sequences
Botanical Journal of the Linnean Linnean Society Society,, 2017,2016. 183 With, 25–38. 2 figures With 2 figures Phylogenetic analyses of Pilosocereus (Cactaceae) inferred from plastid and nuclear sequences ALICE CALVENTE1*, EVANDRO M. MORAES2,PAMELA^ LAVOR1, ISABEL A. S. BONATELLI2, PAMELA NACAGUMA2, LEONARDO M. VERSIEUX1, NIGEL P. TAYLOR3 and DANIELA C. ZAPPI4 1Laboratorio� de Botanica^ Sistematica,� Departamento de Botanica^ e Zoologia, Centro de Biociencias,^ Universidade Federal do Rio Grande do Norte, Campus Central, Lagoa Nova, Natal, CEP 59078-970, RN, Brazil 2 Laboratorio� de Diversidade Genetica� e Evolucßao,~ Departamento de Biologia, Centro de Ciencias^ Humanas e Biologicas,� Universidade Federal de Sao~ Carlos, Sorocaba, Sao~ Paulo, CEP 18052-780, Brazil 3Singapore Botanic Gardens, 1 Cluny Road 259569, Singapore 4Jardim Botanico^ do Rio de Janeiro, Rua Pacheco Leao~ 915, Rio de Janeiro, CEP 22460-030 RJ, Brazil Received 1 March 2016; revised 1 June 2016; accepted for publication 29 August 2016 Pilosocereus is a large genus of Cactaceae with 42 species of columnar cacti distributed in the Americas. In this work we investigate the phylogenetics and evolutionary history of Pilosocereus based in plastid and nuclear DNA sequences. We use phylogenetic trees obtained as a basis to analyse infrageneric relationships and to study the evolution of selected morphological characters and geographical distribution in the group. Thirty-three species of the genus were sampled and five molecular regions were selected, four non-coding intergenic spacers of plastid DNA (trnS-trnG, psbD-trnT, trnL-trnT, petL-psbE) and one nuclear low-copy gene (phytochrome C). The phylogenetic analyses obtained point to a paraphyletic Pilosocereus, with P. -
Florida Keys Terrestrial Adaptation Planning (Keystap) Species
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/330842954 FLORIDA KEYS TERRESTRIAL ADAPTATION PROJECT: Florida Keys Case Study on Incorporating Climate Change Considerations into Conservation Planning and Actions for Threatened and Endang... Technical Report · January 2018 CITATION READS 1 438 6 authors, including: Logan Benedict Jason M. Evans Florida Fish and Wildlife Conservation Commission Stetson University 2 PUBLICATIONS 1 CITATION 87 PUBLICATIONS 983 CITATIONS SEE PROFILE SEE PROFILE Some of the authors of this publication are also working on these related projects: Conservation Clinic View project Vinson Institute Policy Papers View project All content following this page was uploaded by Jason M. Evans on 27 April 2020. The user has requested enhancement of the downloaded file. USFWS Cooperative Agreement F16AC01213 Florida Keys Case Study on Incorporating Climate Change Considerations into Conservation Planning and Actions for Threatened and Endangered Species Project Coordinator: Logan Benedict, Florida Fish and Wildlife Conservation Commission Project Team: Bob Glazer, Florida Fish and Wildlife Conservation Commission Chris Bergh, The Nature Conservancy Steve Traxler, US Fish and Wildlife Service Beth Stys, Florida Fish and Wildlife Conservation Commission Jason Evans, Stetson University Project Report Photo by Logan Benedict Cover Photo by Ricardo Zambrano 1 | Page USFWS Cooperative Agreement F16AC01213 TABLE OF CONTENTS 1. ABSTRACT ............................................................................................................................................................... -
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. -
Espostoa Br.& R
2021/09/25 08:03 1/10 Espostoa Br.& R. Espostoa Br.& R. Cet article est basé sur l'original écrit par Graham Charles et publié dans le British Cactus and Succulent Journal 17(2): 69-79 (1999). Vous en trouverez une traduction sur le Cactus Francophone : Espostoa Br.& R. Il est ici modifié et corrigé à la lumière de nouvelles découvertes. Notez que dans l'article original, la fig 1. à la page 68 a été incorrectement légendée. On doit lire “Espostoa melanostele dans le Canyon Tinajas, près de Lima GC157.04” Although cerei are not the most popular cacti for growers restricted by cultivation in glasshouses, almost all collections have at least one representative of this beautiful genus. Most species are easy to cultivate and the hairy stems of many species make them an attractive addition to any collection, even in a small glasshouse. In pots, they are slower growing than many cerei, a factor which also makes them good show plants, frequently seen winning the Cereus class. For exhibitors, those species with stems covered with white hair catch the judge's eye. The hair can also hide minor blemishes on the stem which would more likely get spotted and count against other less covered species! In keeping with the fashionable trend towards the broader concept of genera, Espostoa has been expanded in recent years to include species previously included in the separate genera Pseudoespostoa Backbg., Thrixanthocereus Backbg. and Vatricania Backbg. Recent molecular studies have shown that Vatricania is not an Espostoa and so it will be excluded from this revised article. -
Tropical Garden Summer 2016
SUMMER 2016 Summer’s bounty in the tropics published by fairchild tropical botanic garden The Shop AT FAIRCHILD GARDENING SUPPLIES | UNIQUE TROPICAL GIFTS | APPAREL HOME DÉCOR | BOOKS | ECO-FRIENDLY AND FAIR-TraDE PRODUCTS ACCESSORIES | TROPICAL GOURMET FOODS | ORCHIDS AND MUCH MORE @ShopatFairchild SHOP HOURS: 9:00 A.M. - 5:30 P.M. SHOP ONLINE AT STORE.FAIRCHILDONLINE.COM contents FEATURES THE WORK OF CONSERVATION 18 37 THE FIGS OF FAIRCHILD DEPARTMENTS 4 FROM THE DIRECTOR 5 FROM THE CHIEF OPERATING OFFICER 7 SCHEDULE OF EVENTS 9 GET IN ON THE CONSERVATION 11 EXPLAINING 14 VIS-A-VIS VOLUNTEERS 17 THE ART IN GARTEN 18 CONSERVING 21 what’s in a name 28 what’s blooming 30 EXPLORING 37 PLANT COLLECTIONS 41 what’s in store 43 PLANT SOCIETIES EXPLORING THE WINDSWEPT 49 EDIBLE GARDENING ISLAND OF GREAT INAGUA 30 50 SOUTH FLORIDA GARDENING 53 BUG BEAT 59 BOOK REVIEW 60 FROM THE ARCHIVES 63 VISTAS 64 GARDEN VIEWS SUMMER 2016 3 from the director ummer at Fairchild is a time when we think about the future, a time for setting plans into motion for the years ahead. It’s when we add new plants to our landscape, launch research projects and develop training programs for our new recruits in botany. Summertime is when our best ideas begin to take shape. SSummertime is also when we keep an extra-vigilant eye on the warm Atlantic tropical waters. During hurricane season, we are constantly aware that everything we do, all of our dreams and hard work, are at risk of being knocked out whenever a storm spins toward South Florida. -
Cactus Explorers Journal
Bradleya 34/2016 pages 100–124 What is a cephalium? Root Gorelick Department of Biology and School of Mathematics & Statistics and Institute of Interdisciplinary Studies, Carleton University, 1125 Raven Road, Ottawa, Ontario K1S 5B6 Canada (e-mail: [email protected]) Photographs by the author unless otherwise stated. Summary : There are problems with previous at - gibt meist einen abgrenzbaren Übergang vom tempts to define ‘cephalium’, such as via produc - photosynthetisch aktiven Gewebe zum nicht pho - tion of more hairs and spines, confluence of tosynthetisch aktiven und blütentragenden areoles, or periderm development at or under - Cephalium, die beide vom gleichen Triebspitzen - neath each areole after flowering. I propose using meristem abstammen. Cephalien haben eine an - the term ‘cephalium’ only for a combination of dere Phyllotaxis als die vegetativen these criteria, i.e. flowering parts of cacti that Sprossabschnitte und sitzen der vorhandenen have confluent hairy or spiny areoles exterior to a vegetativen Phyllotaxis auf. Wenn blühende Ab - thick periderm, where these hairs, spines, and schnitte nur einen Teil der oben genannten Merk - periderms arise almost immediately below the male aufweisen, schlage ich vor, diese Strukturen shoot apical meristem, and with more hairs and als „Pseudocephalien“ zu bezeichnen. spines on reproductive parts than on photosyn - thetic parts of the shoot. Periderm development Introduction and confluent areoles preclude photosynthesis of Most cacti (Cactaceae) are peculiar plants, cephalia, which therefore lack or mostly lack even for angiosperms, with highly succulent stomata. There is almost always a discrete tran - stems, numerous highly lignified leaves aka sition from photosynthetic vegetative tissues to a spines, lack of functional photosynthetic leaves, non-photosynthetic flower-bearing cephalium, CAM photosynthesis, huge sunken shoot apical both of which arise from the same shoot apical meristems, and fantastic stem architectures meristem. -
Genetic Structure of the Florida Key Tree Cactus, Pilosocereus Robinii, Using Restriction Site Associated DNA (RAD) Markers Tonya D
Florida International University FIU Digital Commons FIU Electronic Theses and Dissertations University Graduate School 7-3-2013 Genetic Structure of the Florida Key Tree Cactus, Pilosocereus robinii, using Restriction Site associated DNA (RAD) markers Tonya D. Fotinos [email protected] DOI: 10.25148/etd.FI13080703 Follow this and additional works at: https://digitalcommons.fiu.edu/etd Part of the Genomics Commons, Plant Breeding and Genetics Commons, and the Population Biology Commons Recommended Citation Fotinos, Tonya D., "Genetic Structure of the Florida Key Tree Cactus, Pilosocereus robinii, using Restriction Site associated DNA (RAD) markers" (2013). FIU Electronic Theses and Dissertations. 914. https://digitalcommons.fiu.edu/etd/914 This work is brought to you for free and open access by the University Graduate School at FIU Digital Commons. It has been accepted for inclusion in FIU Electronic Theses and Dissertations by an authorized administrator of FIU Digital Commons. For more information, please contact [email protected]. FLORIDA INTERNATIONAL UNIVERSITY Miami, Florida GENETIC STRUCTURE OF THE FLORIDA KEY TREE CACTUS, Pilosocereus robinii, USING RESTRICTION SITE ASSOCIATED DNA (RAD) MARKERS . A thesis submitted in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE in BIOLOGY By Tonya Dee René Simons Fotinos 2013 To: Dean Kenneth G. Furton College of Arts and Sciences This thesis, written by Tonya Dee René Simons Fotinos, and entitled Genetic Structure of the Florida Key Tree Cactus, Pilosocereus robinii, using Restriction Site associated DNA (RAD) markers, having been approved in respect to style and intellectual content, is referred to you for judgment. We have read this thesis and recommend that it be approved. -
Brasilicereus, Cipocereus, and Pilosocereus in Eastern Brazil
Special Issue: Eastern Brazil ROOT GORELICK Brasilicereus, Cipocereus, and Pilosocereus in eastern Brazil obody goes to Brazil to see Bra- Minas Gerais. These are thin-stemmed, slightly silicereus or Cipocereus. Pilosocer- branched columns covered in short, straight spines. eus is hardly any more popular. Considering how thin the stems are, they remain Indeed, the only species in these remarkably upright, although they may occasion- three genera that most of my ally flop over and rest on rocks or other vegeta- cohorts were anxious to see on tion for support. B. markgrafii is the more dimin- the CSSA field trip was Piloso- utive of the two, with virtually unbranched two- cereus fulvilanatus. Yet plants in meter-tall stems just 1–2 cm in diameter. While all three of these genera are often statuesque and the spines are short and very light brown, they easy to cultivate, and Cipocereus and Pilosocereus can briefly sport a lovely shade of red on new plants often have waxy cuticles in various shades of growth. Closed flower buds are usually green blue and green, large bat-pollinated flowers, and big and have few petals, but the petal tips are red or, fruits that split open to yield brightly colored pulp. rarely, bluish, which seems to hint at the rela- N tionship with Cipocereus. Brasilicereus The more robust species, B. phaeacanthus, usu- ally has chocolate brown spines, from which the Brasilicereus is a genus of two species, B. phaea- name is derived (phaea = brown; canthus = spine). canthus and B. markgrafii, endemic to Bahía and This species branches more, forming plants to L LEFT Brasilicereus markgrafii; these typically upright stems are only 1–2 cm diameter. -
Bradleya 31/2013 Pages 142-149
Bradleya 31/2013 pages 142-149 Coleocephalocereus purpureus has a cephalium; Micrantho - cereus streckeri has a pseudocephalium (Cereeae, Cactoideae, Cactaceae) Root Gorelick Department of Biology, School of Mathematics & Statistics, and Institute of Interdisciplinary Studies Carleton University, 1125 Colonel By Drive, Ottawa, Ontario K1S 5B6 Canada. (email: [email protected]). Photographs by the author Summary : The putatively closely related cactus Introduction genera of Coleocephalocereus , Micranthocereus , Cactaceae (cacti) in the tribe Cactoideae have Cereus , Monvillea , and Stetsonia have a wide a wide range of reproductive anatomies ranging range in specialization of reproductive portions of from cephalia to pseudocephalia to forms where the shoot, from cephalium to pseudocephalium to reproductive and vegetative structures are indis - no specialization. After briefly summarizing the tinguishable (Buxbaum, 1964, 1975; Mauseth, shifting uses of the terms ‘cephalium’ and ‘pseudo - 2006). cephalium’, I provide gross morphological evi - For instance, Melocactus Link & Otto, Disco - dence that Coleocephalocereus purpureus has a cactus Pfeiffer, and Espostoa Britton & Rose have true cephalium that is formed of a continuous true cephalia in which the flowering parts are not swath of bristles and hairs, with its underlying photosynthetic because every epidermal cell con - thick cortex of parenchyma replaced by a narrow tains a modified leaf that is a hair, bristle, or layer of cork. By contrast, Micranthocereus streck - spine, with no stomata amongst the epidermal eri has a pseudocephalium composed of nothing cells (Mauseth, 2006). Furthermore, there are more than larger hairier areoles in which the un - changes to the internal anatomy of cephalia, derlying epidermis is still photosynthetic and the where the underlying cortex is not a wide swath of underlying cortex is still a thick layer of highly succulent parenchyma, but instead a thin parenchyma without any noticeable cork. -
Notes on Florida's Endangered and Threatened Plants 1
NOTES ON FLORIDA'S ENDANGERED AND THREATENED PLANTS 1 Nancy C. Coile2 The Regulated Plant Index is based on information provided by the Endangered Plant Advisory Council (EPAC), a group of seven individuals who represent academic, industry, and environmental interests (Dr. Loran C. Anderson, Dr. Daniel F. Austin,. Mr. Charles D. D aniel III, Mr. David M . Drylie, Jr., Ms. Eve R. Hannahs, Mr. Richard L. Moyroud, and Dr. Daniel B. Ward). Rule Chap. 5B-40, Florida Administrative Code, contains the "Regulated Plant Index" (5B-40.0055) and lists endangered, threatened, and commercially exploited plant species for Florida; defines the categories; lists instances where permits may be issued; and describes penalties for vio lations. Copies of this Rule may be obtained from Florida Department of Agriculture and Consumer Services, Division of Plant Industry, P. O. Box 147100, Gainesville, Fl 32614-7100. Amended 20 September 2000, the "Regulated Plant Index" contains 415 endangered species, 113 threatened species, and eight commercially exploited species. Descriptions of these rare species are often difficult to locate. Florida does not have a single manual covering the flora of the entire state. Long and Lakela s manual (1971) focuses on the area south of Glades County; Clewell (1985) is a guide for the Panhandle; and Wunderlin (1998) is a guide for the entire state of Florida but lacks descriptions. Small (1933) is an excellent resource, but must be used with great care since the nomenclature is outdated and frequently disputed. Clewell (1985) and Wunderlin (1998 ) are guides with keys to the flora, but lack species descriptions. Distribution maps (Wund erlin and Hansen, 200 0) are available over the Internet through the University of South Florida Herbarium [www.plantatlas.usf.edu/]. -
Chapter 14. Wildlife and Forest Communities 341
chapteR 14. Wildlife and Forest Communities 341 Chapter 14. Wildlife and Forest communities Margaret Trani Griep and Beverly Collins1 key FindingS • Hotspot areas for plants of concern are Big Bend National Park; the Apalachicola area of the Southern Gulf Coast; • The South has 1,076 native terrestrial vertebrates: 179 Lake Wales Ridge and the area south of Lake Okeechobee amphibians, 525 birds, 176 mammals, and 196 reptiles. in Peninsular Florida; and coastal counties of North Species richness is highest in the Mid-South (856) and Carolina in the Atlantic Coastal Plain. The Appalachian- Coastal Plain (733), reflecting both the large area of these Cumberland highlands also contain plants identified by subregions and the diversity of habitats within them. States as species of concern. • The geography of species richness varies by taxa. • Species, including those of conservation concern, are Amphibians flourish in portions of the Piedmont and imperiled by habitat alteration, isolation, introduction of Appalachian-Cumberland highlands and across the Coastal invasive species, environmental pollutants, commercial Plain. Bird richness is highest along the coastal wetlands of development, human disturbance, and exploitation. the Atlantic Ocean and Gulf of Mexico, mammal richness Conditions predicted by the forecasts will magnify these is highest in the Mid-South and Appalachian-Cumberland stressors. Each species varies in its vulnerability to highlands, and reptile richness is highest across the forecasted threats, and these threats vary by subregion. Key southern portion of the region. areas of concern arise where hotspots of vulnerable species • The South has 142 terrestrial vertebrate species coincide with forecasted stressors. considered to be of conservation concern (e.g., global • There are 614 species that are presumed extirpated from conservation status rank of critically imperiled, imperiled, selected States in the South; 64 are terrestrial vertebrates or vulnerable), 77 of which are listed as threatened or and 550 are vascular plants.