Low Risk, Unarmed, Tropical Palm, Ornamental, Slow-Growing, Bird-Dispersed
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Biodiversity in Forests of the Ancient Maya Lowlands and Genetic
Biodiversity in Forests of the Ancient Maya Lowlands and Genetic Variation in a Dominant Tree, Manilkara zapota (Sapotaceae): Ecological and Anthropogenic Implications by Kim M. Thompson B.A. Thomas More College M.Ed. University of Cincinnati A Dissertation submitted to the University of Cincinnati, Department of Biological Sciences McMicken College of Arts and Sciences for the degree of Doctor of Philosophy October 25, 2013 Committee Chair: David L. Lentz ABSTRACT The overall goal of this study was to determine if there are associations between silviculture practices of the ancient Maya and the biodiversity of the modern forest. This was accomplished by conducting paleoethnobotanical, ecological and genetic investigations at reforested but historically urbanized ancient Maya ceremonial centers. The first part of our investigation was conducted at Tikal National Park, where we surveyed the tree community of the modern forest and recovered preserved plant remains from ancient Maya archaeological contexts. The second set of investigations focused on genetic variation and structure in Manilkara zapota (L.) P. Royen, one of the dominant trees in both the modern forest and the paleoethnobotanical remains at Tikal. We hypothesized that the dominant trees at Tikal would be positively correlated with the most abundant ancient plant remains recovered from the site and that these trees would have higher economic value for contemporary Maya cultures than trees that were not dominant. We identified 124 species of trees and vines in 43 families. Moderate levels of evenness (J=0.69-0.80) were observed among tree species with shared levels of dominance (1-D=0.94). From the paleoethnobotanical remains, we identified a total of 77 morphospecies of woods representing at least 31 plant families with 38 identified to the species level. -
Samara English Edition 28 (PDF)
ISSUE 28 JANUARy – December 2015 ISSN 1475-8245 saThe Internationalma Newsletter of the Millennium Seedr Banka Partnership www.kew.org/msbp/samara The Australian effort Australia’s large land mass means field experts often work in remote locations. The team at the as part of the MSBP Botanic Gardens and Parks Authority (BGPA) are well By Dr Lucy A. Sutherland set up for long field trips (Australian Seed Bank Partnership, Australian National Botanic Gardens) PHOTO: LUKE SWEEDMAN, BOTANIC GARDENS AND PARKS AUTHORITY Australia was one of the first countries to join the Millennium Seed were commonly for the purpose of supporting the development and Bank Partnership (MSBP). As highlighted by the Global Strategy maintenance of living collections for display and horticulture. Through for Plant Conservation (GSPC 2012) targets, there was a clear need the efforts in Australia, guided by the MSBP, we have seen an expansion for conservation seed banks that provided a safety net for plant of the role of these seed banks into plant conservation. The associated diversity, as well as providing a resource for much needed research on institutions have also increased their conservation efforts, which have often Australia’s native flora. More specifically, the work of seed banking involved greater collaborations with community groups and non-government was needed to enhance knowledge around methods for successful organisations, and the formation of long-term conservation partnerships. species recovery and restoration of plant communities. Reflections by some Australian Partners highlight other aspects of MSBP’s More than three quarters of Australia’s 18,500 flowering plant species are legacy including: endemic and Australia’s dedicated efforts towards in situ conservation are • improving the quality of collections and storage in Australia well recognised. -
Common PALMS of BELIZE Samuel Bridgewater (Natural History Museum, London), Nancy C
1 Common PALMS of BELIZE Samuel Bridgewater (Natural History Museum, London), Nancy C. Garwood (Southern Illinois University, USA) & Steven Brewer (University of North Carolina at Wilmington, USA) Photos by S.G.M Bridgewater, N.C. Garwood, B. Adams (Belize Botanic Gardens) & D. Harris (Royal Botanic Garden Edinburgh). Produced by S.G.M. Bridgewater, N.C. Garwood, with assistance of R.B. Foster, T.S. Wachter, & The Field Museum, Chicago. Support from the UK Darwin Initiative. © Natural History Museum, London: S. Bridgewater [[email protected]] , N.C. Garwood [[email protected]] & S. Brewer [[email protected]] 02/2007 This photoguide covers 25 native species, and 3 Steven Brewer’s Field Key to the Palms of Belize cultivated species of palm commonly provides a complete technical key to all Belizean palms encountered in Belize. It excludes all (41 spp.): Chamaedorea species. These are covered separately in http://www.plantapalm.com/vpe/palmkey/belizekey/bel Rapid Color Guide 195 available from the website: izekey.htm [www.fmnh.org/plantguides]. This photoguide is meant as a field companion to that Useful ID notes and further info. are provided at the work. Another useful source of information is: end of this guide (Sheet 8). Species are presented in Henderson, A. H., G. Galeano & R. Bernal. 1995. Field six major morphological groups (A-F). Guide to the palms of the Americas. Princeton University Press. 1 2 3 4 5 A. PALMS WITH Cryosophila stauracantha PALMATELY (Give-and-take palm) COMPOUND LEAVES Habitat: forest Habit: solitary; tall understorey palm. Stem width: to 10 cm Distribution: widespread ID tip: stems covered in long, branched, often downward pointing spines 6 7 8 C. -
Current Trends and Future Directions in Flower Development Research
Annals of Botany 114: 1399–1406, 2014 doi:10.1093/aob/mcu224, available online at www.aob.oxfordjournals.org VIEWPOINT: PART OF A SPECIAL ISSUE ON FLOWER DEVELOPMENT Current trends and future directions in flower development research Charlie P. Scutt* and Michiel Vandenbussche Laboratoire de Reproduction et De´veloppement des Plantes, (Unite´ mixte de recherche 5667: CNRS-INRA-Universite´ de Lyon), Ecole Normale Supe´rieure de Lyon, 46 alle´e d’Italie, 69364 Lyon Cedex 07, France * For correspondence: E-mail [email protected] Received: 18 September 2014 Accepted: 24 September 2014 Downloaded from Flowers, the reproductive structures of the approximately 400 000 extant species of flowering plants, exist in a tre- mendous range of forms and sizes, mainly due to developmental differences involving the number, arrangement, size and form of the floral organs of which they consist. However, this tremendous diversity is underpinned by a sur- prisingly robust basic floral structure in which a central group of carpels forms on an axis of determinate growth, almost invariably surrounded by two successive zones containing stamens and perianth organs, respectively. Over the last 25 years, remarkable progress has been achieved in describing the molecular mechanisms that control http://aob.oxfordjournals.org/ almost all aspects of flower development, from the phase change that initiates flowering to the final production of fruits and seeds. However, this work has been performed almost exclusively in a small number of eudicot model species, chief among which is Arabidopsis thaliana. Studies of flower development must now be extended to a much wider phylogenetic range of flowering plants and, indeed, to their closest living relatives, the gymnosperms. -
Floral Structure in the Neotropical Palm Genus Chamaedorea (Arecoideae, Arecaceae)
Anales del Jardín Botánico de Madrid Vol. 65(2): 197-210 julio-diciembre 2008 ISSN: 0211-1322 Floral structure in the neotropical palm genus Chamaedorea (Arecoideae, Arecaceae) by Aino Askgaard1, Fred W. Stauffer1, Donald R. Hodel 2, Anders S. Barfod 3 1 Conservatoire et Jardin botaniques, Ch. de l’Impératrice 1, CP 60, CH-1292 Chambésy, Genève, Switzerland [email protected], [email protected] 2 University of California, 4800 E. César E. Chávez Avenue, Los Angeles, CA 90022, USA. [email protected] 3 Department of Biological Sciences, University of Aarhus, Ny Munkegade bygn. 1540, DK-8000 Århus C., Denmark [email protected] (corresponding author) Abstract Resumen Askgaard, A., Stauffer, F.W., Hodel, D.R. &. Barfod, A.S. 2008. Askgaard, A., Stauffer, F.W., Hodel, D.R. &. Barfod, A.S. 2008. Floral structure in the neotropical palm genus Chamaedorea Estructura floral de la palma neotropical del género Chamae- (Arecoideae, Arecaceae). Anales Jard. Bot. Madrid 65(2): 197- dorea (Arecoideae, Arecaceae). Anales Jard. Bot. Madrid 65(2): 210. 197-210 (en inglés). Male and female floral structure has been studied in 28 species Se ha estudiado la estructura de las flores masculinas y femeni- of Chamaedorea, the largest palm genus present in the Neo- nas en 28 especies de Chamaedorea, el género de palmas con tropics. The taxa investigated represent all subgenera according mayor número de especies en la región neotropical. Los táxones to the most recent taxonomic revision of the group. Morpho- investigados representan a todos los subgéneros contemplados logical, histological and cytological features that are known to en la más reciente revisión taxonómica del grupo. -
Complete Inventory
Maya Ethnobotany Complete Inventory of plants 1 Tenth edition, Christmas week December 2011 Maya Ethnobotany Complete Inventory:: fruits,nuts, root crops, grains,construction materials, utilitarian uses, sacred plants, sacred flowers Guatemala, Mexico, Belize, Honduras Nicholas M. Hellmuth Maya Ethnobotany Complete Inventory of plants 2 Introduction This opus is a progress report on over thirty years of studying plants and agriculture of the present-day Maya with the goal of understanding plant usage by the Classic Maya. As a progress report it still has a long way to go before being finished. But even in its unfinished state, this report provides abundant listings of plants in a useful thematic arrangement. The only other publication that I am familiar with which lists even close to most of the plants utilized by the Maya is in an article by Cyrus Lundell (1938). • Obviously books on Mayan agriculture should have informative lists of all Maya agricultural crops, but these do not tend to include plants used for house construction. • There are monumental monographs, such as all the trees of Guatemala (Parker 2008) but they are botanical works, not ethnobotanical, and there is no cross-reference by kind of use. You have to go through over one thousand pages and several thousand tree species to find what you are looking for. • There are even important monographs on Maya ethnobotany, but they are usually limited to one country, or one theme, often medicinal plants. • There are even nice monographs on edible plants of Central America (Chízmar 2009), but these do not include every local edible plant, and their focus is not utilitarian plants at all, nor sacred plants. -
Summary of Plant Protection Regulations Texas Department of Agriculture P.O
TX - 1 of 21 TEXAS (UPDATED AUGUST 2015) SUMMARY OF PLANT PROTECTION REGULATIONS TEXAS DEPARTMENT OF AGRICULTURE P.O. BOX 12847, AUSTIN, TX 78711 (512) 463-7476 For The Hearing Impaired: 1-800-735-2988 (VOICE) or 1-800-735-2989 (TTY) Awinash Bhatkar, Ph.D. .............................. ........................ Coordinator for Biosecurity Programs Phone: (512) 463-5025 Fax: (888) 215-5385 Email: [email protected] Robert Crocker, Ph.D. …………………….Cotton & Citrus Pest Management, and Biotechnology Phone: (512) 463-6332 Email: [email protected] Allison Olofson...……………………………………………………………………. Pest Surveys Phone: (512) 463-7884 Email: [email protected] The information, as provided, is for informational purposes only and should not be interpreted as complete and sufficient to meet regulatory requirements. Coordination with both your state and the destination state plant regulatory agency listed above may be necessary to stay up-to-date on r evised r equir ements. Updated information on the Texas quarantine laws and regulations can be found at www.TexasAgriculture.gov. T he department may perform a quarantine inspection for regulated articles, including plants, vegetables, other agricultural products, or equipment, considered as hosts or carriers of pest s or di seases. NURSERY PRODUCTS AND FLORAL ITEMS Nursery or floral shipments of plant material originating outside of the state must be accompanied by a phytosanitary document applicable to the commodity from the origin state's department of agriculture stating that the plants are free of insect pests and plant diseases. Phytosanitary certification requirements for agricultural commodities and other quarantined arti cl es are provi ded i n speci f i c Texas quaranti nes. -
Potassium (K) Deficiency of Palms
POTASSIUM DEFICIENCY OF PALMS Joe Garofalo*, and Alan Fehrman* Potassium (K) deficiency is a common disorder of growing in clay. K is retained against leaching in those of Mn deficiency (frizzle top) leaf nutrient Table III. Palm disorders/diseases often confused palms in S. Florida. It may be the most widespread & clays & other soils having good cation exchange analysis may be required to distinguish between the with K deficiency. (Compare with Table I.) serious of the non-contagious diseases of palms. capacity, but is readily leached from sands or other two (see Table III.) Most plants that suffer nutrient deficiencies exhibit soils having little cation exchange capacity. It can 1. Disease: various leafspots. Compare to types 1 & 2. various symptoms, some seriously affecting growth; also be induced by a high Nitrogen (N) to K ratio in species: many. but it is rare that a nutrient deficiency kills a plant. the soil. Table I. The 3 types of K deficiency symptoms, & distinction: K deficiency spots appear only on older Among palms, however, some species are very representative species. leaves, whereas disease spots are distributed sensitive to K deficiency, & they will die if it is not Palms growing in containers tend to be susceptible to type of symptom throughout the canopy; nutrient analysis or disease regularly supplied as fertilizer. Manganese (Mn) different deficiencies than landscape palms, & their l. Yellow spots. translucent yellow or orange spots on the lab report may be required. deficiency (“frizzletop”) also will kill palms, & often causes are different. K deficiency can occur in leaflets, which may or may not have small, necrotic 2. -
Pseudophoenix 2021-08: 1–38
PALMARBOR ISSN 2690-3245 Moya López: Pseudophoenix 2021-08: 1–38 A Review of the Nomenclature and Types of Pseudophoenix (Arecaceae) Una Revisión de la Nomenclatura y los Tipos de Pseudophoenix (Arecaceae) CELIO E. MOYA LÓPEZ Abstract The nomenclature and typification of Pseudophoenix, a neotropical genus of four species, are reviewed and updated. Plumier's involvement in the description of P. vinifera is reported and discussed, and unpublished Plumier illustrations of the species present at the National Museum of Natural History in Paris are published. Resumen Se revisa y actualizan la nomenclatura y los tipos de Pseudophoenix, un género neotropical de cuatro especies. Se informa y discute la participación de Plumier en la descripción de P. vinifera, y se publican las ilustraciones inéditas de Plumier de las especies presentes en el Museo Nacional de Historia Natural de París. Introduction Pseudophoenix consists of four species of mostly insular distribution in the Caribbean basin. They are known for their handsome trunks, these often swollen, white, and with attractive, dark, ring- like leaf scars; plumose, pinnate leaves; and infructescences with showy, reddish fruits (Fig. 1). Three species are restricted to the island of Hispaniola, P. ekmanii (southwestern Dominican Republic), P. lediniana (southern Haiti), and P. vinifera (Haiti and Dominican Republic), while the fourth, P. sargentii, the most widely distributed of the four species, occurs in Belize, Cuba, Dominica, Dominican Republic, Haiti, Mexico (Yucatán Peninsula), Puerto Rico, The Bahamas, Turks and Caicos Islands, and U. S . A. (South Florida) (Read 1968, Zona 2020). _____________________________________________________________________________________ 1 PALMARBOR ISSN 2690-3245 Moya López: Pseudophoenix 2021-08: 1–38 1. -
Notes on Cuban Native Palms
Willdenowia 36 – 2006 507 ANGELA LEIVA SÁNCHEZ Notes on Cuban native palms Abstract Leiva Sánchez, A.: Notes on Cuban native palms. – Willdenowia 36 (Special Issue): 507-513. – ISSN 0511-9618; © 2006 BGBM Berlin-Dahlem. doi:10.3372/wi.36.36148 (available via http://dx.doi.org/) A brief, updated account on the taxonomic history of Cuban palms is provided, together with a key for the field identification of the 14 currently recognized native genera. Four of the most interesting genera of Cuban native palms (Thrinax, Coccothrinax, Copernicia and Roystonea) are commented. The name Coccothrinax crinita is lectotypified. Key words: Cuba, Arecaceae, taxonomic history, lectotypification. Introduction Palms are ubiquitous in the Cuban landscape. It is almost impossible to spend a day in this coun- try without seeing at least one palm species. As an indicator of the frequency of palms, 206 geo- graphical localities are named after palms (Leiva 1999). About 81 indigenous palm species in 14 genera are known from the various ecosystems of the island. Since many years Cuban palms have drawn the attention of Cuban scientists as well as those from foreign countries. A brief historical overview The scientific knowledge of Cuban palms began with the discovery and collection of the first palms by Alexander von Humboldt and Aimé Bonpland. They were described and published by Kunth (1815): Cocos crispa Kunth (today: Acrocomia crispa (Kunth) Becc.), Corypha mira- guama Kunth (today: Coccothrinax miraguama (Kunth) Becc.), Oreodoxa regia Kunth (today: Roystonea regia (Kunth) O. F. Cook). These are very common palms in Cuba. Botanists such as C. F. P. -
Pintaud 2015
Université de Montpellier École Doctorale SIBAGHE MÉMOIRE présenté en vue d’obtenir : L’HABILITATION A DIRIGER DES RECHERCHES 2015 Jean-Christophe Pintaud IRD, UMR DIADE/DYNADIV Phylogénie et diversité génétique des palmiers : de la signature du forçage paléoclimatique et géologique à l’empreinte de l’Homme Soutenu le 3 Juillet 2015, Devant le jury composé de : François Bonhomme, Directeur de Recherche CNRS, rapporteur Jérôme Chave, Directeur de Recherche CNRS, rapporteur Dario De Franceschi, Maître de Conférences MNHN, rapporteur Sophie Nadot, Professeur Université de Paris Sud, examinatrice Joëlle Ronfort, chercheur INRA, examinatrice James Tregear, Directeur de Recherche IRD, examinanteur RÉSUMÉ Phylogénie et diversité génétique des palmiers : de la signature du forçage paléoclimatique et géologique à l’empreinte de l’Homme. La famille des palmiers compte 187 genres et environ 2600 espèces, distribués dans toutes les régions chaudes du monde. Les analyses phylogénétiques conduites dans la famille, incorporant des schémas de datation moléculaire calibrés à l’aide de fossiles, montrent de nettes discontinuités dans l’histoire évolutive de ce groupe de plantes au cours du Cénozoïque, coïncidant clairement avec des phénomènes paléoclimatiques et géologiques majeurs. En particulier, un ensemble de phylogénies moléculaires conduites à divers niveaux sur un groupe pris comme modèle, la sous-tribu néotropicale des Bactridinae, nous a permis d’identifier quatre signaux de diversification dans la structure phylogénétique, particulièrement significatifs -
Checklist of the Palms of CELIO E. MOYA López Cuba, with Notes On
PALMS Moya and Leiva: Checklist of Cuban palms Volume 44(2) 2000 Checklist of CELIO E. MOYA LóPEZ Jardín Botánico Sancti Spiritus the Palms of Ministerio de Ciencia, Tecnología y Medio Ambiente Apdo. 52, CP 60200 Cuba, with Sancti Spiritus, Cuba Notes on their [email protected] AND Ecology, ANGELA T. LEIVA SÁNCHEZ Jardín Botánico Nacional Carr. El Rocío, km 3 1/2 Distribution Calabazar, CP 19230 Ciudad de La Habana, Cuba and [email protected] Conservation Cuba has a rich palm flora despite its relatively small territory. The palms play an important role in Cuba's landscape and vegetation and in the everyday life of Cuban people, who have multiple uses for these plants (Muñiz & Borhidi 1982). The goal of this study is to up-date the list of Roystonea (Zona 1996), Sabal (Zona 1990) and Cuban palms given by León (1946), taking into Thrinax (Read 1975), as well as the revision of consideration the revisions of several palm Bactris for the Caribbean (Salzman & Judd 1995). genera from the new world and the new species The most recent additions to the list of palms reported for Cuba. This new checklist will allow from Cuba by Moya et al. (1991), Zona (1992) future publications to use the correct and Borhidi and Hernández (1993) were also nomenclature. included. In preparing this checklist, we reviewed the The family Palmae in Cuba is represented by 15 following lists of Cuban species: Grisebach (1866), genera, two subgenera and 81 species, six hybrids Sauvalle (1868), Beccari (1912, 1913), Dahlgren and nine infraspecific taxa for a total of 96 (1936), León (1946), Alain (1969), Muñiz and indigenous palms (Table 1).