An Analysis of Species Conservation Action Plans in Guinea
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A Casual Cantharophily: the Meeting Between Astylus
Journal of Pollination Ecology, 5(12), 2011, pp 86-89 — Short Communication — A CASUAL CANTHAROPHILY : THE MEETING BETWEEN ASTYLUS VARIEGATUS (C OLEOPTERA : MYLERIDAE ) AND OXYPETALUM BANKSII (A POCYNACEAE : ASCLEPIADOIDEAE ) Milene Faria Vieira* and Rúbia Santos Fonseca Departamento de Biologia Vegetal, Universidade Federal de Viçosa, 36570-000 Viçosa, Minas Gerais, Brazil Abstract —Cantharophily is reported for the first time in a Brazilian asclepiad, involving the mylerid Astylus variegatus and the nectariferous flowers of Oxypetalum banksii , a plant mainly pollinated by wasps. The use of nectar as food by A. variegatus , considered pollinivorous and granivorous, is also novel. The mutual interaction described here is an example of a plant-pollinator interaction with generalist insects visiting a plant with a specialized pollination system. It’s also temporary and occasional and, therefore, is often overlooked in studies of plant-pollinator interactions. In this study, we found that the casual meeting between O. banksii and A. variegatus was a key event for the reproduction of both. Key words: Asclepiad, Atlantic Forest, Brazil, beetles, specialized pollination, wasps The asclepiads (Apocynaceae: Asclepiadoideae, sensu (Asclepias woodii , Sisyranthus trichostomus and Endress & Bruyns 2000) have highly elaborate and Xysmalobium involucratum ) and chafer beetles (Scarabaeidae: complicated flowers. There is an unusual synorganization Cetoniini). Shuttleworth and Johnson (2008) described, also between parts and also between organs of different categories in South Africa, a bimodal pollination system in the asclepiad (Endress 1994). This has led to the evolutionary origin of Xysmalobium undulatum ; its pollination is performed by two new organs that are not present in other angiosperm groups in unrelated species (or functional groups) of pollinators: chafer this combination: corona (more or less well developed beetles and pompilid wasps (Hymenoptera: Pompilidae). -
Challenges of Conservation and Sustainable Management of African Rosewood (Pterocarpus Erinaceus) in West Africa
Chapter Challenges of Conservation and Sustainable Management of African Rosewood (Pterocarpus erinaceus) in West Africa Adjonou Kossi, Houetchegnon Towanou, Rabiou Habou, Segla Kossi Novinyo, Abotsi Komla Elikplim, Johnson Benziwa Nathalie, Alaba Pyoabalo, Ouinsavi Christine A.I. Nougbodé, Quashie Akossiwoa Marie-Luce, Kokutse Adzo Dzifa, Mahamane Ali and Kokou Kouami Abstract Pterocarpus erinaceus is an endemic and threatened plant species in arid and semiarid zones of West Africa and is highly exploited for timber, animal feeding, and various medicinal uses. The species is currently native to the Guinean forest- savannah mosaic ecoregion and reported from Senegal to Cameroon. The values of the main characteristics of the P. erinaceus forest stands (density, average diameter, À average height and average stem height) vary significantly (P < 10 3) from the Guinean zone to the Sahelian zone. It has high technological performance and can be classified as heavy and very hard wood with a density of the order of 0.80 Æ 0.07 g/cm3 and an average hardness of 12 Æ 3.7 g/cm3. The species is the subject of large-scale international traffic between West Africa and Asia, which is by far the greatest threat to the species. The various uses induce repeated mutilation and increase pressures on the species resulting in a significant reduction in its natural populations. In response to this situation, measures are proposed, including large-scale plant production strategies, the definition of minimum felling diameters, policy measures, etc., to meet the restoration needs of natural stands of P. erinaceus and the fight against climate change. Keywords: Pterocarpus erinaceus, socioeconomic services, wood properties, uncontrolled logging, sustainable management, West Africa 1. -
Apocynaceae: Asclepiadoideae)
The pollination and scent ecology of selected Cape milkweeds (Apocynaceae: Asclepiadoideae) Yolanda Tendai Chirango THESIS Submitted in fulfillment of the requirements of the degree of Master of Sciences (Biological Sciences) March 2017 University of Cape Town Supervised by: J. J. Midgely, S-L. Steenhuisen and A. Shuttleworth The copyright of this thesis vests in the author. No quotation from it or information derived from it is to be published without full acknowledgement of the source. The thesis is to be used for private study or non- commercial research purposes only. Published by the University of Cape Town (UCT) in terms of the non-exclusive license granted to UCT by the author. University of Cape Town !!! Name:!Yolanda!Tendai!Chirango! Student!Number:!CHRYOL001! Course:!BIO5010W! !!! !!! Declaration!! !!! I!know!that!plagiarism!is!wrong.!Plagiarism!is!to!use!another’s!work!and!pretend! that!it!is!one’s!own.!! Each!contribution!to,!and!quotation!in,!this!Master’s!Thesis!from!the!work(s)!of! other!people!has!been!attributed,!and!has!been!cited!and!referenced.!! !!! This!thesis!is!my!own!work.!! ! I!have!not!allowed,!and!will!not!allow,!anyone!to!copy!my!work!with!the!intention!of! passing!it!off!as!his!or!her!own!work.!! !!! !!! Signature!______________________________!! Date!___________________13!March!2017_______________!! ! ! 2! ! Acknowledgments ......................................................................................................... 5 Dedication ..................................................................................................................... -
The Evolution of Pollinator–Plant Interaction Types in the Araceae
BRIEF COMMUNICATION doi:10.1111/evo.12318 THE EVOLUTION OF POLLINATOR–PLANT INTERACTION TYPES IN THE ARACEAE Marion Chartier,1,2 Marc Gibernau,3 and Susanne S. Renner4 1Department of Structural and Functional Botany, University of Vienna, 1030 Vienna, Austria 2E-mail: [email protected] 3Centre National de Recherche Scientifique, Ecologie des Foretsˆ de Guyane, 97379 Kourou, France 4Department of Biology, University of Munich, 80638 Munich, Germany Received August 6, 2013 Accepted November 17, 2013 Most plant–pollinator interactions are mutualistic, involving rewards provided by flowers or inflorescences to pollinators. An- tagonistic plant–pollinator interactions, in which flowers offer no rewards, are rare and concentrated in a few families including Araceae. In the latter, they involve trapping of pollinators, which are released loaded with pollen but unrewarded. To understand the evolution of such systems, we compiled data on the pollinators and types of interactions, and coded 21 characters, including interaction type, pollinator order, and 19 floral traits. A phylogenetic framework comes from a matrix of plastid and new nuclear DNA sequences for 135 species from 119 genera (5342 nucleotides). The ancestral pollination interaction in Araceae was recon- structed as probably rewarding albeit with low confidence because information is available for only 56 of the 120–130 genera. Bayesian stochastic trait mapping showed that spadix zonation, presence of an appendix, and flower sexuality were correlated with pollination interaction type. In the Araceae, having unisexual flowers appears to have provided the morphological precon- dition for the evolution of traps. Compared with the frequency of shifts between deceptive and rewarding pollination systems in orchids, our results indicate less lability in the Araceae, probably because of morphologically and sexually more specialized inflorescences. -
Okoubaka Aubrevillei (Pelleg & Norman): a Synthesis of Existing Knowledge for Research and Conservation in West and Central Africa
Journal of Biology and Life Science ISSN 2157-6076 2015, Vol. 6, No. 1 Okoubaka Aubrevillei (Pelleg & Norman): A Synthesis of Existing Knowledge for Research and Conservation in West and Central Africa Temitope Israel Borokini1,2 1Plant Genetic Resources Unit, National Center for Genetic Resources and Biotechnology (NACGRAB), Ibadan, Nigeria 2Program in Ecology, Evolution and Conservation Biology, College of Science, University of Nevada Reno, Reno NV 89557-0314. E-mail: [email protected] Received: October 4, 2014 Accepted: October 21, 2014 doi:10.5296/jbls.v6i1.6399 URL: http://dx.doi.org/10.5296/jbls.v6i1.6399 Abstract Okoubaka aubrevillei is the largest parasitic plant known to man. It is a tropical tree species distributed within West and Central Africa. Concerns were drawn to the tree because of its rarity, disjunct distribution in all its native range, paucity of published scientific information and its hemi-parasitic potentials. This article gathered and synthesized all existing scientific information on the tree to provide a solid foundation for further research on the tree. This article provided detailed information on its name etymology, taxonomic history, and geographical distribution including new locations for the tree, ecological significance and behaviour within its range, supported with an updated map illustrating its distribution within West and Central Africa. The possible causes of its rarity in its range were identified and its hemi-parasitic behaviour was hypothesized. In addition, ethnobotanical uses of the tree, symbolism and dendrolatry, and its significance in modern medicine were extensively discussed. The paper concluded with highlights on prospects for immediate conservation, management and research focus areas for the tree species. -
Foraging Ecology and Conservation Biology of African Elephants: Ecological and Evolutionary Perspectives on Elephant-Woody Plant Interactions in African Landscapes
Foraging ecology and conservation biology of African elephants: Ecological and evolutionary perspectives on elephant-woody plant interactions in African landscapes Item Type Thesis Authors Dudley, Joseph Paine Download date 27/09/2021 15:01:40 Link to Item http://hdl.handle.net/11122/9523 INFORMATION TO USERS This manuscript has been reproduced from the microfilm master. UMI films the text directly from the original or copy submitted. Thus, some thesis and dissertation copies are in typewriter free, while others may be from any type of computer printer. The quality of this reproduction is dependent upon the quality of the copy submitted. Broken or indistinct print, colored or poor quality illustrations and photographs, print bleedthrough, substandard margins, and improper alignment can adversely affect reproduction. In the unlikely event that the author did not send UMI a complete manuscript and there are missing pages, these will be noted. Also, if unauthorized copyright material had to be removed, a note will indicate the deletion. Oversize materials (e.g., maps, drawings, charts) are reproduced by sectioning the original, beginning at the upper left-hand comer and continuing from left to right in equal sections with small overlaps. Each original is also photographed in one exposure and is included in reduced form at the back o f the book. Photographs included in the original manuscript have been reproduced xerographically in this copy. Higher quality 6” x 9” black and white photographic prints are available for any photographs or illustrations appearing in this copy for an additional charge. Contact UMI directly to order. UMI A Bell & Howell Information Company 300 North Zed) Road, Ann Arbor MI 48106-1346 USA 313/761-4700 800/521-0600 Reproduced with permission of the copyright owner. -
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. -
Albuca Spiralis
Flowering Plants of Africa A magazine containing colour plates with descriptions of flowering plants of Africa and neighbouring islands Edited by G. Germishuizen with assistance of E. du Plessis and G.S. Condy Volume 62 Pretoria 2011 Editorial Board A. Nicholas University of KwaZulu-Natal, Durban, RSA D.A. Snijman South African National Biodiversity Institute, Cape Town, RSA Referees and other co-workers on this volume H.J. Beentje, Royal Botanic Gardens, Kew, UK D. Bridson, Royal Botanic Gardens, Kew, UK P. Burgoyne, South African National Biodiversity Institute, Pretoria, RSA J.E. Burrows, Buffelskloof Nature Reserve & Herbarium, Lydenburg, RSA C.L. Craib, Bryanston, RSA G.D. Duncan, South African National Biodiversity Institute, Cape Town, RSA E. Figueiredo, Department of Plant Science, University of Pretoria, Pretoria, RSA H.F. Glen, South African National Biodiversity Institute, Durban, RSA P. Goldblatt, Missouri Botanical Garden, St Louis, Missouri, USA G. Goodman-Cron, School of Animal, Plant and Environmental Sciences, University of the Witwatersrand, Johannesburg, RSA D.J. Goyder, Royal Botanic Gardens, Kew, UK A. Grobler, South African National Biodiversity Institute, Pretoria, RSA R.R. Klopper, South African National Biodiversity Institute, Pretoria, RSA J. Lavranos, Loulé, Portugal S. Liede-Schumann, Department of Plant Systematics, University of Bayreuth, Bayreuth, Germany J.C. Manning, South African National Biodiversity Institute, Cape Town, RSA A. Nicholas, University of KwaZulu-Natal, Durban, RSA R.B. Nordenstam, Swedish Museum of Natural History, Stockholm, Sweden B.D. Schrire, Royal Botanic Gardens, Kew, UK P. Silveira, University of Aveiro, Aveiro, Portugal H. Steyn, South African National Biodiversity Institute, Pretoria, RSA P. Tilney, University of Johannesburg, Johannesburg, RSA E.J. -
Anatomy of the Floral Scape of Bromeliaceae1 SUZANA LÚCIA PROENÇA2,3 and MARIA DAS GRAÇAS SAJO2
Revista Brasil. Bot., V.31, n.3, p.399-408, jul.-set. 2008 Anatomy of the floral scape of Bromeliaceae1 SUZANA LÚCIA PROENÇA2,3 and MARIA DAS GRAÇAS SAJO2 (received: July 04, 2007; accepted: June 05, 2008) ABSTRACT – (Anatomy of the floral scape of Bromeliaceae). This paper describes the anatomy of the floral scape for 12 species of Bromeliaceae, belonging to the subfamilies Bromelioideae, Tillandsioideae and Pitcairnioideae. Although all the scapes have a similar organization, there are variations in the structure of the epidermis, cortex and vascular cylinder. Such variations are described for the studied scapes and, when considered together they can help to identify the species. These aspects are described for each scape and discussed under a taxonomic point of view. Key words - anatomy, Bromeliaceae, floral scape RESUMO – (Anatomia do escapo floral de Bromeliaceae). Este trabalho descreve a anatomia do escapo floral de doze espécies de Bromeliaceae pertencentes às subfamílias Bromelioideae, Tillandsioideae e Pitcairnioideae e tem como objetivo ampliar o conhecimento anatômico da família e desse órgão em particular. Embora todos os escapos apresentem uma organização similar, observam-se variações na estrutura da epiderme, do córtex e do cilindro vascular. Tais variações são descritas para os escapos estudados e, quando são analisadas em conjunto, podem auxiliar na identificação das espécies. Esses aspectos são descritos para cada um dos escapos e discutidos dentro de um contexto taxonômico. Palavras-chave - anatomia, Bromeliaceae, escapo floral Introduction There are few studies on the floral scape anatomy of Bromeliaceae, the more important is Tomlinson’s revision Bromeliaceae comprises about 2,600 Neotropical (1969) of the results of Mez (1896 apud Tomlinson 1969), species, except for Pitcairnia feliciana (A. -
Phylogeny, Adaptive Radiation, and Historical Biogeography in Bromeliaceae: Insights from an Eight-Locus
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/51165827 Phylogeny, Adaptive Radiation, and Historical Biogeography in Bromeliaceae: Insights from an Eight-Locus... Article in American Journal of Botany · May 2011 DOI: 10.3732/ajb.1000059 · Source: PubMed CITATIONS READS 183 290 19 authors, including: Michael H J Barfuss Ralf Horres University of Vienna GenXPro GmbH 37 PUBLICATIONS 1,137 CITATIONS 40 PUBLICATIONS 1,175 CITATIONS SEE PROFILE SEE PROFILE Timothy M. Evans Georg Zizka Grand Valley State University Goethe-Universität Frankfurt am Main and Sen… 27 PUBLICATIONS 1,270 CITATIONS 271 PUBLICATIONS 1,798 CITATIONS SEE PROFILE SEE PROFILE Some of the authors of this publication are also working on these related projects: Genetic Analysis of The Coffea Family View project Phylojive View project All content following this page was uploaded by Thomas J Givnish on 02 June 2014. The user has requested enhancement of the downloaded file. American Journal of Botany 98(5): 872–895. 2011. PHYLOGENY, ADAPTIVE RADIATION, AND HISTORICAL BIOGEOGRAPHY IN BROMELIACEAE: INSIGHTS FROM AN EIGHT-LOCUS PLASTID PHYLOGENY 1 Thomas J. Givnish 2,15 , Michael H. J. Barfuss 3 , Benjamin Van Ee 2,4 , Ricarda Riina 2,5 , Katharina Schulte 6,7 , Ralf Horres 8 , Philip A. Gonsiska 2 , Rachel S. Jabaily 2,9 , Darren M. Crayn 7 , J. Andrew C. Smith 10 , Klaus Winter 11 , Gregory K. Brown 12 , Timothy M. Evans 13 , Bruce K. Holst 14 , Harry Luther 14 , Walter Till 3 , Georg Zizka 6 , Paul E. Berry 5 , and Kenneth J. Sytsma 2 2 Department of Botany, University of Wisconsin-Madison, Madison, Wisconsin 53706 USA; 3 Department of Systematic and Evolutionary Botany, Faculty of Life Sciences, University of Vienna, Vienna A-1030, Austria; 4 Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, Massachusetts 02183 USA; 5 Department of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, Michigan 48109 USA; 6 Department of Botany and Molecular Evolution, Research Institute Senckenberg and J. -
History and Current Status of Systematic Research with Araceae
HISTORY AND CURRENT STATUS OF SYSTEMATIC RESEARCH WITH ARACEAE Thomas B. Croat Missouri Botanical Garden P. O. Box 299 St. Louis, MO 63166 U.S.A. Note: This paper, originally published in Aroideana Vol. 21, pp. 26–145 in 1998, is periodically updated onto the IAS web page with current additions. Any mistakes, proposed changes, or new publications that deal with the systematics of Araceae should be brought to my attention. Mail to me at the address listed above, or e-mail me at [email protected]. Last revised November 2004 INTRODUCTION The history of systematic work with Araceae has been previously covered by Nicolson (1987b), and was the subject of a chapter in the Genera of Araceae by Mayo, Bogner & Boyce (1997) and in Curtis's Botanical Magazine new series (Mayo et al., 1995). In addition to covering many of the principal players in the field of aroid research, Nicolson's paper dealt with the evolution of family concepts and gave a comparison of the then current modern systems of classification. The papers by Mayo, Bogner and Boyce were more comprehensive in scope than that of Nicolson, but still did not cover in great detail many of the participants in Araceae research. In contrast, this paper will cover all systematic and floristic work that deals with Araceae, which is known to me. It will not, in general, deal with agronomic papers on Araceae such as the rich literature on taro and its cultivation, nor will it deal with smaller papers of a technical nature or those dealing with pollination biology. -
Adaptive Radiation, Correlated and Contingent Evolution, and Net Species Diversification in Bromeliaceae
Molecular Phylogenetics and Evolution 71 (2014) 55–78 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Adaptive radiation, correlated and contingent evolution, and net species diversification in Bromeliaceae Thomas J. Givnish a,*, Michael H.J. Barfuss b, Benjamin Van Ee c, Ricarda Riina d, Katharina Schulte e,f, Ralf Horres g, Philip A. Gonsiska a, Rachel S. Jabaily h, Darren M. Crayn f, J. Andrew C. Smith i, Klaus Winter j, Gregory K. Brown k, Timothy M. Evans l, Bruce K. Holst m, Harry Luther n, Walter Till b, Georg Zizka e, Paul E. Berry o, Kenneth J. Sytsma a a Department of Botany, University of Wisconsin-Madison, Madison, WI 53706, USA b Department of Systematic and Evolutionary Botany, Faculty of Life Sciences, University of Vienna, Vienna A-1030, Austria c School of Natural Sciences, Black Hills State University, Spearfish, SD 57799, USA d Real Jardín Botánico, CSIC, Plaza de Murillo 2, Madrid 28014, Spain e Department of Botany and Molecular Evolution, Research Institute Senckenberg and J.W. Goethe University, Frankfurt am Main D-60325, Germany f Australian Tropical Herbarium, James Cook University, Cairns, QLD 4878, Australia g GenXPro, Frankfurt am Main 60438, Germany h Department of Biology, Rhodes College, Memphis, TN 38112, USA i Department of Plant Sciences, University of Oxford, Oxford OX1 3RB, United Kingdom j Smithsonian Tropical Research Institute, Balboa, Ancon, Republic of Panama k Department of Botany, University of Wyoming, Laramie, WY 82071, USA l Department of Biology, Grand Valley State University, Allendale, MI 49401, USA m Marie Selby Botanical Gardens, Sarasota, FL 34236, USA n Gardens By The Bay, National Parks Board Headquarters, Singapore 259569, Singapore o Department of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, MI 48109, USA article info abstract Article history: We present an integrative model predicting associations among epiphytism, the tank habit, entangling Received 22 May 2013 seeds, C3 vs.