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Plant Species and Functional Diversity Along Altitudinal Gradients, Southwest Ethiopian Highlands
Plant Species and Functional Diversity along Altitudinal Gradients, Southwest Ethiopian Highlands Dissertation Zur Erlangung des akademischen Grades Dr. rer. nat. Vorgelegt der Fakultät für Biologie, Chemie und Geowissenschaften der Universität Bayreuth von Herrn Desalegn Wana Dalacho geb. am 08. 08. 1973, Äthiopien Bayreuth, den 27. October 2009 Die vorliegende Arbeit wurde in dem Zeitraum von April 2006 bis October 2009 an der Universität Bayreuth unter der Leitung von Professor Dr. Carl Beierkuhnlein erstellt. Vollständiger Abdruck der von der Fakultät für Biologie, Chemie und Geowissenschaften der Universität Bayreuth zur Erlangung des akademischen Grades eines Doktors der Naturwissenschaften genehmigten Dissertation. Prüfungsausschuss 1. Prof. Dr. Carl Beierkuhnlein (1. Gutachter) 2. Prof. Dr. Sigrid Liede-Schumann (2. Gutachter) 3. PD. Dr. Gregor Aas (Vorsitz) 4. Prof. Dr. Ludwig Zöller 5. Prof. Dr. Björn Reineking Datum der Einreichung der Dissertation: 27. 10. 2009 Datum des wissenschaftlichen Kolloquiums: 21. 12. 2009 Contents Summary 1 Zusammenfassung 3 Introduction 5 Drivers of Diversity Patterns 5 Deconstruction of Diversity Patterns 9 Threats of Biodiversity Loss in the Ttropics 10 Objectives, Research Questions and Hypotheses 12 Synopsis 15 Thesis Outline 15 Synthesis and Conclusions 17 References 21 Acknowledgments 27 List of Manuscripts and Specification of Own Contribution 30 Manuscript 1 Plant Species and Growth Form Richness along Altitudinal Gradients in the Southwest Ethiopian Highlands 32 Manuscript 2 The Relative Abundance of Plant Functional Types along Environmental Gradients in the Southwest Ethiopian highlands 54 Manuscript 3 Land Use/Land Cover Change in the Southwestern Ethiopian Highlands 84 Manuscript 4 Climate Warming and Tropical Plant Species – Consequences of a Potential Upslope Shift of Isotherms in Southern Ethiopia 102 List of Publications 135 Declaration/Erklärung 136 Summary Summary Understanding how biodiversity is organized across space and time has long been a central focus of ecologists and biogeographers. -
ISSN: 2230-9926 International Journal of Development Research Vol
Available online at http://www.journalijdr.com s ISSN: 2230-9926 International Journal of Development Research Vol. 10, Issue, 11, pp. 41819-41827, November, 2020 https://doi.org/10.37118/ijdr.20410.11.2020 RESEARCH ARTICLE OPEN ACCESS MELLIFEROUS PLANT DIVERSITY IN THE FOREST-SAVANNA TRANSITION ZONE IN CÔTE D’IVOIRE: CASE OF TOUMODI DEPARTMENT ASSI KAUDJHIS Chimène*1, KOUADIO Kouassi1, AKÉ ASSI Emma1,2,3, et N'GUESSAN Koffi1,2 1Université Félix Houphouët-Boigny (Côte d’Ivoire), U.F.R. Biosciences, 22 BP 582 Abidjan 22 (Côte d’Ivoire), Laboratoire des Milieux Naturels et Conservation de la Biodiversité 2Institut Botanique Aké-Assi d’Andokoi (IBAAN) 3Centre National de Floristique (CNF) de l’Université Félix Houphouët-Boigny (Côte d’Ivoire) ARTICLE INFO ABSTRACT Article History: The melliferous flora around three apiaries of 6 to 10 hives in the Department of Toumodi (Côte Received 18th August, 2020 d’Ivoire) was studied with the help of floristic inventories in the plant formations of the study Received in revised form area. Observations were made within a radius of 1 km around each apiary in 3 villages of 22nd September, 2020 Toumodi Department (Akakro-Nzikpli, Bédressou and N'Guessankro). The melliferous flora is Accepted 11th October, 2020 composed of 157 species in 127 genera and 42 families. The Fabaceae, with 38 species (24.20%) th Published online 24 November, 2020 is the best represented. Lianas with 40 species (25.48%) and Microphanerophytes (52.23%) are the most predominant melliferous plants in the study area. They contain plants that flower during Key Words: the rainy season (87 species, i.e. -
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. -
Plastid and Nuclear DNA Markers.Pdf
Molecular Phylogenetics and Evolution 51 (2009) 238–258 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Plastid and nuclear DNA markers reveal intricate relationships at subfamilial and tribal levels in the soapberry family (Sapindaceae) Sven Buerki a,*, Félix Forest b, Pedro Acevedo-Rodríguez c, Martin W. Callmander d,e, Johan A.A. Nylander f, Mark Harrington g, Isabel Sanmartín h, Philippe Küpfer a, Nadir Alvarez a a Institute of Biology, University of Neuchâtel, Rue Emile-Argand 11, CH-2009 Neuchâtel, Switzerland b Molecular Systematics Section, Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3DS, United Kingdom c Department of Botany, Smithsonian Institution, National Museum of Natural History, NHB-166, Washington, DC 20560, USA d Missouri Botanical Garden, PO Box 299, 63166-0299, St. Louis, MO, USA e Conservatoire et Jardin botaniques de la ville de Genève, ch. de l’Impératrice 1, CH-1292 Chambésy, Switzerland f Department of Botany, Stockholm University, SE-10691, Stockholm, Sweden g School of Marine and Tropical Biology, James Cook University, PO Box 6811, Cairns, Qld 4870, Australia h Department of Biodiversity and Conservation, Real Jardin Botanico – CSIC, Plaza de Murillo 2, 28014 Madrid, Spain article info abstract Article history: The economically important soapberry family (Sapindaceae) comprises about 1900 species mainly found Received 21 May 2008 in the tropical regions of the world, with only a few genera being restricted to temperate areas. The inf- Revised 27 November 2008 rafamilial classification of the Sapindaceae and its relationships to the closely related Aceraceae and Hip- Accepted 23 January 2009 pocastanaceae – which have now been included in an expanded definition of Sapindaceae (i.e., subfamily Available online 30 January 2009 Hippocastanoideae) – have been debated for decades. -
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. -
Sapindaceae): Evidence from Molecular Sequence Data
Philippine Journal of Systematic Biology Vol. V (June 2011) SEARCHING FOR THE RELATIVES OF THE PHILIPPINE ENDEMIC Gloeocarpus Radlk. (SAPINDACEAE): EVIDENCE FROM MOLECULAR SEQUENCE DATA AXEL H. ARRIOLA1,3 and GRECEBIO JONATHAN D. ALEJANDRO2,3 1Department of Biological Sciences, College of Arts and Sciences, University of the East, 2219 C.M. Recto Ave, Manila, Philippines, 2College of Science and Research Center for Natural Sciences, and 3The Graduate School, University of Santo Tomas, Espana, Manila, 1015 Philippines ABSTRACT Gloeocarpus is a monotypic genus and is endemic to the Philippines. There are no available molecular data for Gloeocarpus, and its generic status as well as its position within the Sapindaceae has never been challenged, hence, it was not included in any molecular phylogenetic study within the family. Therefore, to determine its phylogenetic position and to evaluate its monophyly, the ITS (nrDNA) regions were sequenced and analyzed together with the previously published sequences of closely related genera. The aligned ITS dataset contained a total of 694 positions, 239 of which are parsimony informative. The strict consensus tree confirmed the phylogenetic position of Gloeocarpus within the tribe Cupanieae with strong support (BS=100) and the monophyly of the genus is highly supported (BS=100). Molecular results support morphological evidences characterizing the genus by having the sinuous branchlets and hairy petals with folded margin. INTRODUCTION Sapindaceae s.l. (soapberry family) is a cosmopolitan family with c.142 genera and 1900 species of trees, shrubs and lianas that are widely distributed within the tropical region but with some temperate representatives (Acer L. and Aesculus L.) (Buerki et al., 2010). -
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.