Impact of Ethnobotanical Utilization on the Population Structure of Androstachys Johnsonii Prain
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Pollen Ultrastructure of the Biovulate Euphorbiaceae Author(S): Michael G
Pollen Ultrastructure of the Biovulate Euphorbiaceae Author(s): Michael G. Simpson and Geoffrey A. Levin Reviewed work(s): Source: International Journal of Plant Sciences, Vol. 155, No. 3 (May, 1994), pp. 313-341 Published by: The University of Chicago Press Stable URL: http://www.jstor.org/stable/2475184 . Accessed: 26/07/2012 14:35 Your use of the JSTOR archive indicates your acceptance of the Terms & Conditions of Use, available at . http://www.jstor.org/page/info/about/policies/terms.jsp . JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact [email protected]. The University of Chicago Press is collaborating with JSTOR to digitize, preserve and extend access to International Journal of Plant Sciences. http://www.jstor.org Int.J. Plant Sci. 155(3):313-341.1994. ? 1994by The Universityof Chicago. All rightsreserved. 1058-5893/94/5503-0008$02.00 POLLENULTRASTRUCTURE OF THE BIOVULATE EUPHORBIACEAE MICHAEL G. SIMPSON AND GEOFFREY A. LEVIN' Departmentof Biology,San Diego StateUniversity, San Diego,California 92182-0057; and BotanyDepartment, San Diego NaturalHistory Museum, P.O. Box 1390,San Diego,California 92112 Pollenultrastructure of the biovulate Euphorbiaceae, including the subfamilies Phyllanthoideae and Oldfieldioideae,was investigatedwith light, scanning electron, and transmissionelectron microscopy. Pollenof Phyllanthoideae, represented by 12 speciesin ninegenera, was prolateto oblate,almost always 3-colporate,rarely 3-porate or pantoporate,and mostlywith reticulate, rarely baculate, echinate, or scabrate,sculpturing. -
Picrodendraceae1
Flora of South Australia 5th Edition | Edited by Jürgen Kellermann PICRODENDRACEAE1 T.M. Spokes2 & J.Z. Weber3 Shrubs, much branched subshrubs (or trees); latex absent; monoecious (in S.A.) or dioecious; indumentum simple; stipules present or absent; leaves shortly petiolate, alternate, opposite or whorled, simple (in S.A.) or palmate, entire (in S.A.) or toothed. Flowers usually small, unisexual, axillary or subterminal, solitary or in few-flowered fascicles, sessile or shortly pedicellate, apetalous; sepals (2) 4–6 (10+); male flowers with 3, 4, 6 (9–40) stamens, often with a small lobed disc within the staminate whorl, interspersed between it, or stamens inserted in cavities of the disc (or disc absent); filaments free or variously united, anthers dorsifixed, basifixed or sessile, longitudinally dehiscent; female flowers 2- or 3-, rarely up to 5-celled, ovary superior with 2 ovules per cell, styles 2 or 3 (–5), variously united either basally or to half way, disc annular and shallowly lobed or absent. Fruit a capsule, dehiscent (in S.A.), rarely indehiscent; seeds 2 per locule or 1 per locule by abortion; caruncle present (in S.A.) or absent; endosperm usually copious. A small pantropical family especially in the SW Pacific, extending N to the southern United States and S to southern Australia. The family contains 26 genera and c. 80 species worldwide, 9 genera and 34 species in Australia, 2 genera and 2 species in S.A. Picrodendraceae contains some species of economic use for timber (Androstachys Prain, Piranhea Baill.); Aboriginal Australians use the bitter bark of Petalostigma F.Muell. spp. -
Flora of South Australia 5Th Edition | Edited by Jürgen Kellermann
Flora of South Australia 5th Edition | Edited by Jürgen Kellermann PICRODENDRACEAE1 T.M. Spokes2 & J.Z. Weber3 Shrubs, much branched subshrubs (or trees); latex absent; monoecious (in S.A.) or dioecious; indumentum simple; stipules present or absent; leaves shortly petiolate, alternate, opposite or whorled, simple (in S.A.) or palmate, entire (in S.A.) or toothed. Flowers usually small, unisexual, axillary or subterminal, solitary or in few-flowered fascicles, sessile or shortly pedicellate, apetalous; sepals (2) 4–6 (10+); male flowers with 3, 4, 6 (9–40) stamens, often with a small lobed disc within the staminate whorl, interspersed between it, or stamens inserted in cavities of the disc (or disc absent); filaments free or variously united, anthers dorsifixed, basifixed or sessile, longitudinally dehiscent; female flowers 2- or 3-, rarely up to 5-celled, ovary superior with 2 ovules per cell, styles 2 or 3 (–5), variously united either basally or to half way, disc annular and shallowly lobed or absent. Fruit a capsule, dehiscent (in S.A.), rarely indehiscent; seeds 2 per locule or 1 per locule by abortion; caruncle present (in S.A.) or absent; endosperm usually copious. A small pantropical family especially in the SW Pacific, extending N to the southern United States and S to southern Australia. The family contains 26 genera and c. 80 species worldwide, 9 genera and 34 species in Australia, 2 genera and 2 species in S.A. Picrodendraceae contains some species of economic use for timber (Androstachys Prain, Piranhea Baill.); Aboriginal Australians use the bitter bark of Petalostigma F.Muell. spp. -
Journal Arnold Arboretum
JOURNAL OF THE ARNOLD ARBORETUM HARVARD UNIVERSITY G. SCHUBERT T. G. HARTLEY PUBLISHED BY THE ARNOLD ARBORETUM OF HARVARD UNIVERSITY CAMBRIDGE, MASSACHUSETTS DATES OF ISSUE No. 1 (pp. 1-104) issued January 13, 1967. No. 2 (pp. 105-202) issued April 16, 1967. No. 3 (pp. 203-361) issued July 18, 1967. No. 4 (pp. 363-588) issued October 14, 1967. TABLE OF CONTENTS COMPARATIVE MORPHOLOGICAL STUDIES IN DILLENL ANATOMY. William C. Dickison A SYNOPSIS OF AFRICAN SPECIES OF DELPHINIUM J Philip A. Munz FLORAL BIOLOGY AND SYSTEMATICA OF EUCNIDE Henry J. Thompson and Wallace R. Ernst .... THE GENUS DUABANGA. Don M. A. Jayaweera .... STUDIES IX SWIFTENIA I MKUACKAE) : OBSERVATION UALITY OF THE FLOWERS. Hsueh-yung Lee .. SOME PROBLEMS OF TROPICAL PLANT ECOLOGY, I Pompa RHIZOME. Martin H. Zimmermann and P. B Two NEW AMERICAN- PALMS. Harold E. Moure, Jr NOMENCLATURE NOTES ON GOSSYPIUM IMALVACE* Brizicky A SYNOPSIS OF THE ASIAN SPECIES OF CONSOLIDA CEAE). Philip A. Munz RESIN PRODUCER. Jean H. Langenheim COMPARATIVE MORPHOLOGICAL STUDIES IN DILLKNI POLLEN. William C. Dickison THE CHROMOSOMES OF AUSTROBAILLVA. Lily Eudi THE SOLOMON ISLANDS. George W. G'dUtt A SYNOPSIS OF THE ASIAN SPECIES OF DELPII STRICTO. Philip A. Munz STATES. Grady L. Webster THE GENERA OF EUPIIORBIACEAE IN THE SOT TUFA OF 1806, AN OVERLOOI EST. C. V. Morton REVISION OF THE GENI Hartley JOURNAL OF THE ARNOLD ARBORETUM HARVARD UNIVERSITY T. G. HARTLEY C. E. WOOD, JR. LAZELLA SCHWARTEN Q9 ^ JANUARY, 1967 THE JOURNAL OF THE ARNOLD ARBORETUM Published quarterly by the Arnold Arboretum of Harvard University. Subscription price $10.00 per year. -
Using the Checklist N W C
Using the checklist • The arrangement of the checklist is alphabetical by family followed by genus, grouped under Pteridophyta, Gymnosperms, Monocotyledons and Dicotyledons. • All species and synonyms are arranged alphabetically under genus. • Accepted names are in bold print while synonyms or previously-used names are in italics. • In the case of synonyms, the currently used name follows the equals sign (=), and only refers to usage in Zimbabwe. • Distribution information is included under the current name. • The letters N, W, C, E, and S, following each listed taxon, indicate the known distribution of species within Zimbabwe as reflected by specimens in SRGH or cited in the literature. Where the distribution is unknown, we have inserted Distr.? after the taxon name. • All species known or suspected to be fully naturalised in Zimbabwe are included in the list. They are preceded by an asterisk (*). Species only known from planted or garden specimens were not included. Mozambique Zambia Kariba Mt. Darwin Lake Kariba N Victoria Falls Harare C Nyanga Mts. W Mutare Gweru E Bulawayo GREAT DYKEMasvingo Plumtree S Chimanimani Mts. Botswana N Beit Bridge South Africa The floristic regions of Zimbabwe: Central, East, North, South, West. A checklist of Zimbabwean vascular plants A checklist of Zimbabwean vascular plants edited by Anthony Mapaura & Jonathan Timberlake Southern African Botanical Diversity Network Report No. 33 • 2004 • Recommended citation format MAPAURA, A. & TIMBERLAKE, J. (eds). 2004. A checklist of Zimbabwean vascular plants. -
Albany Thicket Biome
% S % 19 (2006) Albany Thicket Biome 10 David B. Hoare, Ladislav Mucina, Michael C. Rutherford, Jan H.J. Vlok, Doug I.W. Euston-Brown, Anthony R. Palmer, Leslie W. Powrie, Richard G. Lechmere-Oertel, Şerban M. Procheş, Anthony P. Dold and Robert A. Ward Table of Contents 1 Introduction: Delimitation and Global Perspective 542 2 Major Vegetation Patterns 544 3 Ecology: Climate, Geology, Soils and Natural Processes 544 3.1 Climate 544 3.2 Geology and Soils 545 3.3 Natural Processes 546 4 Origins and Biogeography 547 4.1 Origins of the Albany Thicket Biome 547 4.2 Biogeography 548 5 Land Use History 548 6 Current Status, Threats and Actions 549 7 Further Research 550 8 Descriptions of Vegetation Units 550 9 Credits 565 10 References 565 List of Vegetation Units AT 1 Southern Cape Valley Thicket 550 AT 2 Gamka Thicket 551 AT 3 Groot Thicket 552 AT 4 Gamtoos Thicket 553 AT 5 Sundays Noorsveld 555 AT 6 Sundays Thicket 556 AT 7 Coega Bontveld 557 AT 8 Kowie Thicket 558 AT 9 Albany Coastal Belt 559 AT 10 Great Fish Noorsveld 560 AT 11 Great Fish Thicket 561 AT 12 Buffels Thicket 562 AT 13 Eastern Cape Escarpment Thicket 563 AT 14 Camdebo Escarpment Thicket 563 Figure 10.1 AT 8 Kowie Thicket: Kowie River meandering in the Waters Meeting Nature Reserve near Bathurst (Eastern Cape), surrounded by dense thickets dominated by succulent Euphorbia trees (on steep slopes and subkrantz positions) and by dry-forest habitats housing patches of FOz 6 Southern Coastal Forest lower down close to the river. -
Gene Tree Estimation Error, Incomplete Lineage Sorting, and Ancient Gene
bioRxiv preprint doi: https://doi.org/10.1101/2020.05.26.112318; this version posted May 27, 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. 1 The Perfect Storm: 2 Gene Tree Estimation Error, Incomplete Lineage Sorting, and Ancient Gene 3 Flow Explain the Most Recalcitrant Ancient Angiosperm Clade, Malpighiales 4 5 Liming Cai1, Zhenxiang Xi1,2, Emily Moriarty Lemmon3, Alan R. Lemmon4, Austin Mast3, 6 Christopher E. Buddenhagen3,5, Liang Liu6, Charles C. Davis1 7 8 1 Department of Organismic and Evolutionary Biology, Harvard University Herbaria, 9 Cambridge, MA 02138, USA; 10 2 Key Laboratory of Bio-Resource and Eco-Environment of Ministry of Education, College of 11 Life Sciences, Sichuan University, Chengdu 610065, China; 12 3 Department of Biological Sciences, 319 Stadium Dr., Florida State University, Tallahassee, 13 FL 32306, USA; 14 4 Department of Scientific Computing, Florida State University, Tallahassee, FL 32306, USA; 15 5 AgResearch, 10 Bisley Road, Hamilton 3214, New Zealand 16 6 Department of Statistics and Institute of Bioinformatics, University of Georgia, Athens, GA 17 30602, USA; 18 19 Corresponding author: 20 Liming Cai, Department of Organismic and Evolutionary Biology, Harvard University 21 Herbaria, Cambridge, MA 02138, USA; E-mail: [email protected] bioRxiv preprint doi: https://doi.org/10.1101/2020.05.26.112318; this version posted May 27, 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. -
Euphorbiaceae Sl, Malpighiales
Pl. Syst. Evol. 261: 187–215 (2006) DOI 10.1007/s00606-006-0414-0 Female flowers and systematic position of Picrodendraceae (Euphorbiaceae s.l., Malpighiales) D. Merino Sutter1, P. I. Forster2, and P. K. Endress1 1Institute of Systematic Botany, University of Zurich, Zurich, Switzerland 2Queensland Herbarium, Environmental Protection Agency, Brisbane Botanic Gardens, Toowong, Queensland, Australia Received December 2, 2005; accepted January 5, 2006 Published online: May 9, 2006 Ó Springer-Verlag 2006 Abstract. This is the first comparative study of large obturator, and (4) explosive fruits with floral structure of the recently established new carunculate seeds. family Picrodendraceae (part of Euphorbiaceae s.l.) in Malpighiales. Nine species of eight (out of Key words: Picrodendraceae, Euphorbiaceae, ca. 28) genera were studied. Female flowers are Phyllanthaceae, Malpighiales, floral structure, mainly completely trimerous, and in such flowers perianth, gynoecium, ovules. the perianth consists of one or two whorls of sepals. A floral disc (which probably functions as a nectary) is mostly present. The free parts of the Introduction carpels are simple (unbranched) in all ten species Euphorbiaceae in the broad, classical sense studied. Each carpel contains two crassinucellar, anatropous or hemitropous, epitropous (antitro- (here referred to as ‘Euphorbiaceae s.l.’) are a pous) ovules, which are covered by a large greatly diverse group, comprising over 300 obturator. The inner integument is thicker than genera and about 8000 species (Webster 1994a, the outer (equally thick in two species studied), b; Radcliffe-Smith 2001). Various classification and commonly both integuments form the micro- systems have been proposed by different pyle. In mature ovules the vascular bundle authors. -
Wood Atlas of the Euphorbiaceae Sl
1 Author – Title 1 Westra & Koek-Noorman — Wood Atlas of the Euphorbiaceae s. l. 1 Wood Atlas of the Euphorbiaceae s.l. by Lubbert Y. Th. Westra and Jifke Koek-Noorman Nationaal Herbarium Nederland, Utrecht University branch Heidelberglaan 2, 3584 CS Utrecht, The Netherlands IAWA Journal Supplement 4 — 2004 Published for the International Association of Wood Anatomists at the Nationaal Herbarium Nederland, The Netherlands ISSN 0928-1541 ISBN 90-71236-60-9 Lubbert Y.Th. Westra and Jifke Koek-Noorman Wood Atlas of the Euphorbiaceae s.l. IAWA Journal Supplement 4 — 2004 Published for he International Association of Wood Anatomists at the Nationaal Herbarium Nederland P.O. Box 9514 – 2300 RA Leiden – The Netherlands Cover: Aleurites moluccana (L.) Willd. (Uw 24065), see Figure 7d. Contents Introduction ........................................................................................................... 4 About the book ..................................................................................................... 4 Materials and methods ....................................................................................... 5 What information can be retrieved from the pictures? .......................... 5 Growth rings ..................................................................................................... 6 Vessels ................................................................................................................ 6 Axial parenchyma .......................................................................................... -
Phylogenetic Implications of Pollen Ultrastructure in the Oldfieldioideae (Euphorbiaceae) Author(S): Geoffrey A
Phylogenetic Implications of Pollen Ultrastructure in the Oldfieldioideae (Euphorbiaceae) Author(s): Geoffrey A. Levin and Michael G. Simpson Source: Annals of the Missouri Botanical Garden, Vol. 81, No. 2 (1994), pp. 203-238 Published by: Missouri Botanical Garden Press Stable URL: http://www.jstor.org/stable/2992094 Accessed: 13-04-2015 18:50 UTC Your use of the JSTOR archive indicates your acceptance of the Terms & Conditions of Use, available at http://www.jstor.org/page/info/about/policies/terms.jsp JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact [email protected]. Missouri Botanical Garden Press is collaborating with JSTOR to digitize, preserve and extend access to Annals of the Missouri Botanical Garden. http://www.jstor.org This content downloaded from 146.244.235.206 on Mon, 13 Apr 2015 18:50:29 UTC All use subject to JSTOR Terms and Conditions PHYLOGENETIC GeoffreyA. Levin2 and Michael G. Simpson3 IMPLICATIONSOF POLLEN ULTRASTRUCTUREIN THE OLDFIELDIOIDEAE (EUPHORBIACEAE)1 ABSTRACT The pollen structure of members of Euphorbiaceae subfamilies Oldfieldioideaeand Phyllanthoideae was studied using scanning and transmission electron microscopy in order to assess taxonomic relationships. We identified 10 palynological characters that appear to have systematic significance. We also identified 37 characters of vegetative morphology and anatomy, mostly based on data obtained by Hayden, and five characters of reproductive morphology, based on data in the literature. -
Long-Term Morphological Stasis Maintained by a Plant–Pollinator Mutualism
Long-term morphological stasis maintained by a plant–pollinator mutualism Charles C. Davisa,1, Hanno Schaefera,b, Zhenxiang Xia, David A. Baumc, Michael J. Donoghued,1, and Luke J. Harmone aDepartment of Organismic and Evolutionary Biology, Harvard University Herbaria, Harvard University, Cambridge, MA 02138; bDepartment of Ecology and Ecosystem Management, Technische Universitaet Muenchen, D-85354 Freising, Germany; cDepartment of Botany, University of Wisconsin–Madison, Madison, WI 53706; dDepartment of Ecology and Evolutionary Biology, Yale University, New Haven, CT 06520; and eDepartment of Biological Sciences, University of Idaho, Moscow, ID 83844 Contributed by Michael J. Donoghue, February 27, 2014 (sent for review April 28, 2012) Many major branches in the Tree of Life are marked by stereotyped Neotropical representatives that produce floral oils and are vis- body plans that have been maintained over long periods of time. ited by these three oil-collecting bee tribes. None of them, One possible explanation for this stasis is that there are genetic or however, are as diverse as Malpighiaceae, which are also the developmental constraints that restrict the origin of novel body oldest of the seven oil-bee–pollinated clades (17). plans. An alternative is that basic body plans are potentially quite Malpighiaceae provide a natural test of the role of intrinsic labile, but are actively maintained by natural selection. We present versus extrinsic factors in generating morphological stasis; this is evidence that the conserved floral morphology of a species-rich particularly relevant in the context of Anderson’s earlier hy- flowering plant clade, Malpighiaceae, has been actively main- pothesis outlined above, but also more generally in the context of tained for tens of millions of years via stabilizing selection imposed developmental constraints that have been hypothesized to limit by their specialist New World oil-bee pollinators. -
Systematic Anatomy of Euphorbiaceae Subfamily Oldfieldioideae I
University of Richmond UR Scholarship Repository Biology Faculty Publications Biology 1994 Systematic Anatomy of Euphorbiaceae Subfamily Oldfieldioideae I. Overview W. John Hayden University of Richmond, [email protected] Follow this and additional works at: http://scholarship.richmond.edu/biology-faculty-publications Part of the Botany Commons, Other Plant Sciences Commons, and the Plant Biology Commons Recommended Citation Hayden, W. John. "Systematic Anatomy of Euphorbiaceae Subfamily Oldfieldioideae I. Overview." Annals of the Missouri Botanical Garden 81, no. 2 (1994): 180-202. This Article is brought to you for free and open access by the Biology at UR Scholarship Repository. It has been accepted for inclusion in Biology Faculty Publications by an authorized administrator of UR Scholarship Repository. For more information, please contact [email protected]. SYSTEMATIC ANATOMY OF W.John Hayden2 EUPHORBIACEAE SUBFAMILY OLDFIELDIOIDEAE. I. OVERVIEW' ABSTRACT The biovulate subfamily Oldfieldioideaeof Euphorbiaceae, characterized by spiny pollen, is an otherwise apparently diverse assemblage of mostly Southern Hemisphere trees and shrubs that traditionally have been allied with genera of Phyllanthoideae and Porantheroideae sensu Pax and Hoffmann. Although fairly diverse anatomically, the following structures characterize the subfamily with only a few exceptions: pinnate brochidodromousvenation with generally randomly organized tertiary and higher order venation; foliar and petiolar glands absent; unicellular or unbranched