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Cactus (Opuntia Spp.) As Forage 169
Cactus (Opuntia spp.) as forage 169 Food •••A.gricultv,.. Org•nU.taon or United -N••lon• FAO Cactus (Opuntiaspp.) PLANT PRODUCTION as forage AND PROTECTlON PAPER 169 Ed~ed by Candelario Mondragon-Jacobo lnstituto Nacional de Investigaciones Forestales y Agropecuarias (INIFAP) Mexico and Salvador Perez-Gonzalez Universidad Aut6noma de Queretaro Mexico Coordinated for FAD by Enrique Arias Horticultural Crops Group Stephen G. Reynolds Grassland and Pasture Crops Group FAO Plant Production and Protection Division and Manuel D. sanchez Feed Resources Group FAO Animal Production and HeaHh Division Produced within the frameworl< of the FAO International Technical Cooperation Networl< ot on Cactus Pear ••u nttttd• NaUon• Rome,2001 Reprinted 2002 The designations “developed” and “developing” economies are intended for statistical convenience and do not necessarily express a judgement about the stage reached by a particular country, country territory or area in the development process. The views expressed herein are those of the authors and do not necessarily represent those of the Food and Agriculture Organization of the United Nations or of their affiliated organization(s). The designations employed and the presentation of material in this information product do not imply the expression of any opinion whatsoever on the part of the Food and Agriculture Organization of the United Nations concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. ISBN 92-5-104705-7 All rights reserved. Reproduction and dissemination of material in this information product for educational or other non-commercial purposes are authorized without any prior written permission from the copyright holders provided the source is fully acknowledged. -
Plant Associations and Descriptions for American Memorial Park, Commonwealth of the Northern Mariana Islands, Saipan
National Park Service U.S. Department of the Interior Natural Resource Stewardship and Science Vegetation Inventory Project American Memorial Park Natural Resource Report NPS/PACN/NRR—2013/744 ON THE COVER Coastal shoreline at American Memorial Park Photograph by: David Benitez Vegetation Inventory Project American Memorial Park Natural Resource Report NPS/PACN/NRR—2013/744 Dan Cogan1, Gwen Kittel2, Meagan Selvig3, Alison Ainsworth4, David Benitez5 1Cogan Technology, Inc. 21 Valley Road Galena, IL 61036 2NatureServe 2108 55th Street, Suite 220 Boulder, CO 80301 3Hawaii-Pacific Islands Cooperative Ecosystem Studies Unit (HPI-CESU) University of Hawaii at Hilo 200 W. Kawili St. Hilo, HI 96720 4National Park Service Pacific Island Network – Inventory and Monitoring PO Box 52 Hawaii National Park, HI 96718 5National Park Service Hawaii Volcanoes National Park – Resources Management PO Box 52 Hawaii National Park, HI 96718 December 2013 U.S. Department of the Interior National Park Service Natural Resource Stewardship and Science Fort Collins, Colorado The National Park Service, Natural Resource Stewardship and Science office in Fort Collins, Colorado, publishes a range of reports that address natural resource topics. These reports are of interest and applicability to a broad audience in the National Park Service and others in natural resource management, including scientists, conservation and environmental constituencies, and the public. The Natural Resource Report Series is used to disseminate high-priority, current natural resource management information with managerial application. The series targets a general, diverse audience, and may contain NPS policy considerations or address sensitive issues of management applicability. All manuscripts in the series receive the appropriate level of peer review to ensure that the information is scientifically credible, technically accurate, appropriately written for the intended audience, and designed and published in a professional manner. -
Carbon and Water Balances for Young Fruits of Platyopuntias
PHYSIOLOGIA PLANTARUM 109: 160–166. 2000 Copyright © Physiologia Plantarum 2000 Printed in Ireland—all rights reser6ed ISSN 0031-9317 Carbon and water balances for young fruits of platyopuntias Park S. Nobel* and Erick De la Barrera Department of Organismic Biology, Ecology, and E6olution, Uni6ersity of California, Los Angeles, CA 90095-1606, USA *Corresponding author, e-mail: [email protected] Received 27 July 1999; revised 13 December 1999 Questions relating to transpired versus retained water for pected for CAM plants. The water potential of the young fruits, the xylem versus the phloem as water supplier to the fruits (average of −0.41 MPa) was higher than that of the fruits, and the importance of fruit photosynthesis for fruit cladodes (average of −0.60 MPa), indicating that water dry mass gain were examined in the field for 6 species of entered the fruits via the phloem rather than via the xylem. platyopuntias (Nopalea cochenillifera, Opuntia ficus-indica, Solution entry into the fruits via the phloem supplied the O. megacantha, O. robusta, O. streptacantha and O. undu- water lost by transpiration and allowed for increases in fruit lata), cacti with flattened stem segments (cladodes). For fresh mass (daily transpiration averaged 3.2-fold higher than plants with fruits midway between floral bud appearance and daily water content increases), while the accumulating so- fruit maturation, transpiration was greater at night for the lutes were apparently polymerized to account for the higher cladodes, as expected for Crassulacean acid metabolism water potentials of the fruits compared with the cladodes. (CAM) plants, but greater during the daytime for the fruits The phloem thus acts as the sole supplier of water and the of all 6 species. -
Botany for the Herbalist Common Plant Families 7Song, Director Northeast School of Botanical Medicine 7Song.Com
Botany for the Herbalist Common Plant Families 7Song, Director Northeast School of Botanical Medicine 7Song.com This handout describes common plant families in the US and Canada. Each family segment contains general characteristics of the family as well as some of the more commonly known species within. In some families such as the Liliaceae, the genera of the plants are still in transition and being placed in newly created families. In other families such as the Scrophulariaceae, some of the former genera have been placed into different already existing families. Within this handout they are generally kept in the older family grouping with the new family identified next to the genus. Field botany is the study of identifying plants and grouping them into categories based on shared anatomical characteristics. Much of this is based on their reproductive parts, especially their flowers. One of the most useful starting points to identify specific plants in the field is by knowing their plant families. Families are a useful category to understand, as plants within them may share obvious traits both botanical (anatomical similarities) and other qualities such as aromatics. As far as medicinal characteristics within a family, there are generally more exceptions to shared traits than similarities in uses. An example showing both sides this is the Apiaceae. This family includes many aromatic, flavorful plants such as Dill, Fennel, and Angelica but also Poison hemlock (Conium), a notoriously poisonous plant. Another example is the Liliaceae with edible foods such as garlic, onion and asparagus but also the toxic Veratrum and Lily-of-the-valley (Convallaria). -
Mission to the Caribbean-Final Report
THE STATUS OF CACTOBLASTIS CACTORUM (LEPIDOPTERA: PYRALIDAE) IN THE CARIBBEAN AND THE LIKELIHOOD OF ITS SPREAD TO MEXICO Report* to the International Atomic Energy Agency (IAEA), Joint FAO/IAEA Division of Nuclear Techniques in Food and Agriculture and the Plant Health General Directorate, Mexico (DGSVB/SAGARPA) as part of the TC Project MEX/5/029 Helmuth G. Zimmermann¹, Mayra Pérez Sandi y Cuen² and Arturo Bello Rivera³ ¹Helmuth Zimmermann & Associates, Pretoria, South Africa. ² Consultant to SAGARPA, Mexico D.F. ³SAGARPA, Plant Health, Mexico D.F. © IAEA 2005 The islands surveyed during this mission included: Puerto Rico, Dominican Republic, Antigua, Montserrat, St. Kitts, Jamaica and Grand Cayman (funded by the IAEA). *This report also includes information and conclusions by the second author (Mayra Perez Sandi) who visited and surveyed the following islands in the Lesser Antilles: Guadeloupe, Dominique, Trinidad and Tobago, Chacachacare, Grenada, St. Vicent, Bequia, Barbados, St. Lucia, Martinique and Chevalier. This part of the survey was funded by PRONATURA NORESTE, FMCN Y USAID. 1 EXECUTIVE SUMMARY The cactus moth, Cactoblastis cactorum (Berg) , which has become the textbook example of successful biological weed control of invasive Opuntia species in many countries, including some Caribbean islands, is now threatening not only the lucrative cactus pear industry in Mexico, but also the rich diversity of all Opuntia species in most of the North American mainland. Already threatened species in Mexico could go extinct. The moth is now present on most Caribbean islands as a consequence of mostly deliberate or accidental introductions by man, or through natural spread. Although there is convincing evidence that Cactoblastis reached Florida inadvertently conveyed by the nursery trade, there also exists the slight possibility of natural spread and by means of cyclonic weather events. -
North American Botanic Garden Strategy for Plant Conservation 2016-2020 Botanic Gardens Conservation International
Nova Southeastern University NSUWorks Marine & Environmental Sciences Faculty Reports Department of Marine and Environmental Sciences 1-1-2016 North American Botanic Garden Strategy for Plant Conservation 2016-2020 Botanic Gardens Conservation International American Public Gardens Association Asociacion Mexicana de Jardines Center for Plant Conservation Plant Conservation Alliance See next page for additional authors Find out more information about Nova Southeastern University and the Halmos College of Natural Sciences and Oceanography. Follow this and additional works at: https://nsuworks.nova.edu/occ_facreports Part of the Plant Sciences Commons Authors Botanic Gardens Conservation International, American Public Gardens Association, Asociacion Mexicana de Jardines, Center for Plant Conservation, Plant Conservation Alliance, Pam Allenstein, Robert Bye, Jennifer Ceska, John Clark, Jenny Cruse-Sanders, Gerard Donnelly, Christopher Dunn, Anne Frances, David Galbraith, Jordan Golubov, Gennadyi Gurman, Kayri Havens, Abby Hird Meyer, Douglas Justice, Edelmira Linares, Maria Magdalena Hernandez, Beatriz Maruri Aguilar, Mike Maunder, Ray Mims, Greg Mueller, Jennifer Ramp Neale, Martin Nicholson, Ari Novy, Susan Pell, John J. Pipoly III, Diane Ragone, Peter Raven, Erin Riggs, Kate Sackman, Emiliano Sanchez Martinez, Suzanne Sharrock, Casey Sclar, Paul Smith, Murphy Westwood, Rebecca Wolf, and Peter Wyse Jackson North American Botanic Garden Strategy For Plant Conservation 2016-2020 North American Botanic Garden Strategy For Plant Conservation 2016-2020 Acknowledgements Published January 2016 by Botanic Gardens Conservation International. Support from the United States Botanic Garden, the American Public Gardens Association, and the Center for Plant Conservation helped make this publication possible. The 2016-2020 North American Botanic Garden Strategy for Plant Conservation is dedicated to the late Steven E. Clemants, who so diligently and ably led the creation of the original North American Strategy published in 2006. -
Research Notes
Research Notes GEOGRAPHICAL DISTRIBUTION AND HOST PLANTS OF THE CACTUS MOTH, CACTOBLASTIS CACTORUM (BERG) IN PUERTO RICO AND THE UNITED STATES VIRGIN ISLANDS The cactus moth, Caddblastis cadorum (Berg)1, was described from Argentina in 1885 in the genus Zophodia. Ragonot2 transferred the species to the genus Caddblastis in his 1901 monograph. C. cadorum occurs endemically in the more northern provinces of Argen tina: Entre Ríos, Corrientes, Santa Fe, the northern part of Córdoba, Santiago del Estero, Tucumán, Salta, Juyuy and the Chaco. In Uruguay, it has been recorded along the Uruguay and Plata Rivers from Piriápolis in the south, northward to Salta. The distribution extends from Corrientes in northeastern Argentina northward through Paraguay, where the insect has been observed at Villa de la Concepción and in the vicinity of Asunción, into the Brazilian province of Matto Grosso, where the larva has been recorded at Corumba on the Paraguay River. Heinrich3'4 discussed this species taxonomically in his 1939 and 1956 revisions of the moths belonging to the Phycitinae (Lepidoptera). The most complete account on the biological control of this species was given by Dodd6 in 1940, while Mann6 in 1969 furnished an excellent account of the distribution, host plants and biology of C. cadorum. Simmonds and Bennett7 in 1966 discussed the introduction and host plants of the moth into the Leeward Islands of the West Indies (Nevis, Montserrat, Antigua, St. Kitts). The eggs of Caddblastis cadorum are laid in chains or egg sticks generally at the end of a cactus spine (fig. 1, A). It is well known that larvae (fig. -
Section 1. Western White Pine (Pinus Monticola)
40 - PART 1. CONSENSUS DOCUMENTS ON BIOLOGY OF TREES Section 1. Western white pine (Pinus monticola) 1. Taxonomy The largest genus in the family Pinaceae, Pinus L., which consists of about 110 pine species, occurs naturally through much of the Northern Hemisphere, from the far north to the cooler montane tropics (Peterson, 1980; Richardson, 1998). Two subgenera are usually recognised: hard pines (generally with much resin, wood close-grained, leaf fascicle sheath persistent, two fibrovascular bundles per needle — the diploxylon pines); and soft, or white pines (generally little resin, wood coarse-grained, sheath sheds early, one fibrovascular bundle in a needle — the haploxylon pines). These subgenera are called respectively subgenus Pinus and subgenus Strobus (Little and Critchfield, 1969; Price et al., 1998; Gernandt et al., 2005). Occasionally, one to about half the species (20 spp.) in subgenus Strobus have been classified instead in a variable subgenus Ducampopinus. Western white pine (Pinus monticola Dougl. ex D. Don) belongs to subgenus Strobus (Syring et al., 2007). Pinus monticola was classified by Critchfield and Little (1966) as one of 14 white pines in section Strobus, subsection Strobi, now call section Ouinquefoliae and subsection Strobus, respectively. Earlier classifications have varied in the number of species assigned to subsection Strobus, but P. monticola has consistently been grouped with the New World species P. ayacahuite, P. lambertiana, and P. strobus and the Old World species P. wallichiana (synonym P. griffithii) and P. peuce (Critchfield, 1986). A molecular phylogeny of the genus Pinus, based on the nuclear ribosomal DNA internal transcribed spacer (nrITS), did not support separation of subsection Strobus from either subsection Cembrae or subsection Krempfianae (Liston et al., 1999). -
Quarantine Host Range and Natural History of Gadirtha Fusca, a Potential Biological Control Agent of Chinese Tallowtree (Triadica Sebifera) in North America
DOI: 10.1111/eea.12737 Quarantine host range and natural history of Gadirtha fusca, a potential biological control agent of Chinese tallowtree (Triadica sebifera) in North America Gregory S. Wheeler1* , Emily Jones1, Kirsten Dyer1, Nick Silverson1 & Susan A. Wright2 1USDA/ARS Invasive Plant Research Laboratory, 3225 College Ave., Ft Lauderdale, FL 33314, USA, and 2USDA/ARS Invasive Plant Research Laboratory, Gainesville, FL 32608, USA Accepted: 23 August 2018 Key words: biocontrol, classical biological control, weed control, Euphorbiaceae, defoliating caterpillar, host range tests, invasive weeds, Sapium, Lepidoptera, Nolidae, integrated pest management, IPM Abstract Classical biological control can provide an ecologically sound, cost-effective, and sustainable manage- ment solution to protect diverse habitats. These natural and managed ecosystems are being invaded and transformed by invasive species. Chinese tallowtree, Triadica sebifera (L.) Small (Euphorbiaceae), is one of the most damaging invasive weeds in the southeastern USA, impacting wetlands, forests, and natural areas. A defoliating moth, Gadirtha fusca Pogue (Lepidoptera: Nolidae), was discovered feeding on Chinese tallowtree leaves in the weed’s native range and has been tested for its suitability as a biological control agent. Natural history studies of G. fusca indicated that the neonates have five instars and require 15.4 days to reach pupation. Complete development from egg hatch to adult emergence required 25.8 days. No differences were found between males and females in terms of life history and nutritional indices measured. Testing of the host range of G. fusca larvae was conducted with no-choice, dual-choice, and multigeneration tests and the results indicated that this species has a very narrow host range. -
Insights Into Chloroplast Genome Variation Across Opuntioideae (Cactaceae)
bioRxiv preprint doi: https://doi.org/10.1101/2020.03.06.981183; this version posted March 8, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Insights into chloroplast genome variation across Opuntioideae (Cactaceae) Matias Köhler1,2, Marcelo Reginato1, Tatiana T. Souza-Chies1, Lucas C. Majure2,3 1 – Programa de Pós-Graduação em Botânica, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil. 2 – University of Florida Herbarium (FLAS), Florida Museum of Natural History, Gainesville, Florida, United States. 3 – Department of Research, Conservation and Collections, Desert Botanical Garden, Phoenix, Arizona, United States. Abstract Chloroplast genomes (plastomes) are frequently treated as highly conserved among land plants. However, many lineages of vascular plants have experienced extensive structural rearrangements, including inversions and modifications to the size and content of genes. Cacti are one of these lineages, containing the smallest plastome known for an obligately photosynthetic angiosperm, including the loss of one copy of the inverted repeat (~25 kb) and the ndh genes suite, but only a few cacti from the subfamily Cactoideae have been sufficiently characterized. Here, we investigated the variation of plastome sequences across the second-major lineage of the Cactaceae, the subfamily Opuntioideae, to address 1) how variable is the content and arrangement of chloroplast genome sequences across the subfamily, and 2) how phylogenetically informative are the plastome sequences for resolving major relationships among the clades of Opuntioideae. -
Crafting and Consuming an American Sonoran Desert: Global Visions, Regional Nature and National Meaning
Crafting and Consuming an American Sonoran Desert: Global Visions, Regional Nature and National Meaning Item Type text; Electronic Dissertation Authors Burtner, Marcus Publisher The University of Arizona. Rights Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author. Download date 02/10/2021 04:13:17 Link to Item http://hdl.handle.net/10150/268613 CRAFTING AND CONSUMING AN AMERICAN SONORAN DESERT: GLOBAL VISIONS, REGIONAL NATURE AND NATIONAL MEANING by Marcus Alexander Burtner ____________________________________ copyright © Marcus Alexander Burtner 2012 A Dissertation Submitted to the Faculty of the DEPARTMENT OF HISTORY In Partial Fulfillment of the Requirements for the degree of DOCTOR OF PHILOSOPHY In the Graduate College THE UNIVERSITY OF ARIZONA 2012 2 THE UNIVERSITY OF ARIZONA GRADUATE COLLEGE As members of the Dissertation Committee, we certify that we have read the dissertation prepared by Marcus A. Burtner entitled “Crafting and Consuming an American Sonoran Desert: Global Visions, Regional Nature, and National Meaning.” and recommend that it be accepted as fulfilling the dissertation requirement for the Degree of Doctor of Philosophy ____________________________________________________________Date: 1/7/13 Katherine Morrissey ____________________________________________________________Date: 1/7/13 Douglas Weiner ____________________________________________________________Date: 1/7/13 Jeremy Vetter ____________________________________________________________Date: 1/7/13 Jack C. Mutchler Final approval and acceptance of this dissertation is contingent upon the candidate's submission of the final copies of the dissertation to the Graduate College. I hereby certify that I have read this dissertation prepared under my direction and recommend that it be accepted as fulfilling the dissertation requirement. -
From Cacti to Carnivores: Improved Phylotranscriptomic Sampling And
Article Type: Special Issue Article RESEARCH ARTICLE INVITED SPECIAL ARTICLE For the Special Issue: Using and Navigating the Plant Tree of Life Short Title: Walker et al.—Phylotranscriptomic analysis of Caryophyllales From cacti to carnivores: Improved phylotranscriptomic sampling and hierarchical homology inference provide further insight into the evolution of Caryophyllales Joseph F. Walker1,13, Ya Yang2, Tao Feng3, Alfonso Timoneda3, Jessica Mikenas4,5, Vera Hutchison4, Caroline Edwards4, Ning Wang1, Sonia Ahluwalia1, Julia Olivieri4,6, Nathanael Walker-Hale7, Lucas C. Majure8, Raúl Puente8, Gudrun Kadereit9,10, Maximilian Lauterbach9,10, Urs Eggli11, Hilda Flores-Olvera12, Helga Ochoterena12, Samuel F. Brockington3, Michael J. Moore,4 and Stephen A. Smith1,13 Manuscript received 13 October 2017; revision accepted 4 January 2018. 1 Department of Ecology & Evolutionary Biology, University of Michigan, 830 North University Avenue, Ann Arbor, MI 48109-1048 USA 2 Department of Plant and Microbial Biology, University of Minnesota-Twin Cities, 1445 Gortner Avenue, St. Paul, MN 55108 USA 3 Department of Plant Sciences, University of Cambridge, Cambridge CB2 3EA, UK 4 Department of Biology, Oberlin College, Science Center K111, 119 Woodland Street, Oberlin, OH 44074-1097 USA 5 Current address: USGS Canyonlands Research Station, Southwest Biological Science Center, 2290 S West Resource Blvd, Moab, UT 84532 USA 6 Institute of Computational and Mathematical Engineering (ICME), Stanford University, 475 Author Manuscript Via Ortega, Suite B060, Stanford, CA, 94305-4042 USA This is the author manuscript accepted for publication and has undergone full peer review but has not been through the copyediting, typesetting, pagination and proofreading process, which may lead to differences between this version and the Version of Record.