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BIOL/APBI 324 – Introduction to Seed Plant Taxonomy
This syllabus is a general representation of the course as previously offered and is subject to change. BIOL/APBI 324 – Introduction to Seed Plant Taxonomy General Course Syllabus (as of September 2019) About the Course: Course Description: An introduction to seed plant taxonomy emphasizing descriptive morphology and identification. Each student will be required to submit a plant collection. Correct understanding of the actual relationships between plants, rather than superficial resemblance, is the basis of comparative biology required to analyze the diversity of plant forms. The species diversity of plants is considerable, and this course will pay particular attention to very diverse and important groups such as the grasses and the orchids, focusing on reasons for their evolutionary success. Identification skills will be inculcated by the lectures working in tandem with the laboratory sessions. This course aims to give students a good working knowledge of plant taxonomy as a preparation for work in any biological discipline. Course Format: Lecture and Laboratory Credits: 3 Pre-requisites: BIOL 121 Course Learning Objectives: By the end of this course, students will be able to: • Achieve a good working knowledge of concepts, principles, and recent discoveries in plant taxonomy. • Gain an overview of seed plant diversity, including the most species-rich plant families and so be able to place any botanical information in the overall context of plant diversity. • Learn ways in which their knowledge can be applied to ecology and evolutionary biology. • Gain an appreciation of how current research in the field is being done by reading recent research papers. Textbooks and Additional Resources: Laboratory fee: $25; please bring to first lab. -
Principles of Plant Taxonomy, V.*
THE OHIO JOURNAL OF SCIENCE VOL. XXVIII MARCH, 1928 No. 2 PRINCIPLES OF PLANT TAXONOMY, V.* JOHN H. SCHAFFNER, Ohio State University. After studying the taxonomy of plants for twenty-five years the very remarkable fact became evident that there is no general correspondence of the taxonomic system with the environment, but as the great paleontologist, Williams, said in 1895: "environmental conditions are but the medium through which organic evolution has been determinately ploughing its way." Of course, the very fact that there is a system of phylogenetic relationships of classes, orders, families, and genera and that these commonly have no general correspondence to environment shows that, in classifying the plant material, we must discard all notions of teleological, utilitarian, and selective factors as causative agents of evolution. The general progressive movement has been carried on along quite definite lines. The broader and more fundamental changes appeared first and are practically constant, and on top of these, .potentialities or properties of smaller and smaller value have been introduced, until at the end new factors of little general importance alone are evolved. These small potentialities are commonly much less stable than the more fundamental ones and thus great variability in subordinate characters is often present in the highest groups. We must then think of the highest groups as being full of hereditary potentialities while the lower groups have comparatively few. As stated above, there is a profound non-correspondence of the .taxonomic system and the various orthogenetic series with the environment. The system of plants, from the taxonomic point of view, is non-utilitarian. -
Ecology and Management of Larix Forests: a Look Ahead Proceedings of an International Symposium
Ecology and Management of Larix Forests: A Look Ahead Proceedings of an International Symposium Whitefish, Montana, U.S.A. October 5-9, 1992 Compilers: Wyman C. Schmidt Kathy J. McDonald Duchesne, L. C.; Lelu, M. A; von Aderkas, P.; Charest, Klimaszewska, K 1989. Plantlet development from imma P. J. 1992. Microprojectile-mediated DNA delivery in ture zygotic embryos of hybrid larch through somatic haploid and diploid embryogenic cells of Larix spp. embryogenesis. Plant Science. 63: 95-103. Canadian Journal of Forest Research. [In press]. Klimaszewska, K; Ward, C.; Cheliak, W. M. 1992. Cryo Ellis, D. D.; McCabe, D.; McInnis, S.; Martinell, B.; preservation and plant regeneration from embryogenic Roberts, D.; McCown, B. 1991. Transformation of white cultures oflarch (Larix x eurolepis) and black spruce spruce by electrical discharge particle acceleration. In: (Picea mariana). Journal of Expermental Botany. 43: Haissing, B. E.; Kirk, T. K; Olsen, W. L.; Raffa, K F.; 73-79. Slavicek, J. M., eds. Applications of biotechnology-to Lelu, M. A; Klimaszewska, K K; Jones, C.; Ward, C.; tree culture, protection and utilization. United States von Aderkas, P.; Charest, P. J. 1992. A laboratory guide Department of Agriculture, Forest Service, Columbus, to somatic embryogenesis in spruce and larch. Petawawa OH:I02. National Forestry Institute. Information Report. Huang, Y.; Diner, AM.; Karnosky, D. F. 1991. Agrobacter PI-X-Ul (submitted for publication). ium rhizogenes-mediated genetic transformation and von Aderkas, P.; Klimaszewska, K K; Bonga, J . M. 1990. regeneration of a conifer: oorix decidua. In: Vitro Cell. Diploid and haploid embryogenesis in Larix leptolepis, Dev. BioI. 27P: 201-207. -
Principles of Plant Taxonomy Bot
PRINCIPLES OF PLANT TAXONOMY BOT 222 Dr. M. Ajmal Ali, PhD 1 What is Taxonomy / Systematics ? Animal group No. of species Amphibians 6,199 Birds 9,956 Fish 30,000 Mammals 5,416 Tundra Reptiles 8,240 Subtotal 59,811 Grassland Forest Insects 950,000 Molluscs 81,000 Q: Why we keep the stuffs of our home Crustaceans 40,000 at the fixed place or arrange into some Corals 2,175 kinds of system? Desert Others 130,200 Rain forest Total 1,203,375 • Every Human being is a Taxonomist Plants No. of species Mosses 15,000 Ferns and allies 13,025 Gymnosperms 980 Dicotyledons 199,350 Monocotyledons 59,300 Green Algae 3,715 Red Algae 5,956 Lichens 10,000 Mushrooms 16,000 Brown Algae 2,849 Subtotal 28,849 Total 1,589,361 • We have millions of different kind of plants, animals and microorganism. We need to scientifically identify, name and classify all the living organism. • Taxonomy / Systematics is the branch of science deals with classification of organism. 2 • Q. What is Plant Taxonomy / Plant systematics We study plants because: Plants convert Carbon dioxide gas into Every things we eat comes Plants produce oxygen. We breathe sugars through the process of directly or indirectly from oxygen. We cannot live without photosynthesis. plants. oxygen. Many chemicals produced by the Study of plants science helps to Study of plants science helps plants used as learn more about the natural Plants provide fibres for paper or fabric. to conserve endangered medicine. world plants. We have millions of different kind of plants, animals and microorganism. -
Complete Chloroplast Genome of Japanese Larch (Larix Kaempferi): Insights Into Intraspecific Variation with an Isolated Northern Limit Population
Article Complete Chloroplast Genome of Japanese Larch (Larix kaempferi): Insights into Intraspecific Variation with an Isolated Northern Limit Population Shufen Chen 1, Wataru Ishizuka 2, Toshihiko Hara 3 and Susumu Goto 1,* 1 Education and Research Center, The University of Tokyo Forests, Graduate School of Agricultural and Life Sciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-8657, Japan; [email protected] 2 Forestry Research Institute, Hokkaido Research Organization, Koushunai, Bibai, Hokkaido 079-0166, Japan; [email protected] 3 Institute of Low Temperature Science, Hokkaido University, Sapporo-city, Hokkaido 060-0819, Japan; [email protected] * Correspondence: [email protected]; Tel.: +81-3-5841-5493 Received: 25 July 2020; Accepted: 11 August 2020; Published: 14 August 2020 Abstract: Research Highlights: The complete chloroplast genome for eight individuals of Japanese larch, including from the isolated population at the northern limit of the range (Manokami larch), revealed that Japanese larch forms a monophyletic group, within which Manokami larch can be phylogenetically placed in Japanese larch. We detected intraspecific variation for possible candidate cpDNA markers in Japanese larch. Background and Objectives: The natural distribution of Japanese larch is limited to the mountainous range in the central part of Honshu Island, Japan, with an isolated northern limit population (Manokami larch). In this study, we determined the phylogenetic position of Manokami larch within Japanese larch, characterized the chloroplast genome of Japanese larch, detected intraspecific variation, and determined candidate cpDNA markers. Materials and Methods: The complete genome sequence was determined for eight individuals, including Manokami larch, in this study. -
Cupressaceae Et Taxodiaceae
AVERTISSEMENT Ce document est le fruit d'un long travail approuvé par le jury de soutenance et mis à disposition de l'ensemble de la communauté universitaire élargie. Il est soumis à la propriété intellectuelle de l'auteur. Ceci implique une obligation de citation et de référencement lors de l’utilisation de ce document. D'autre part, toute contrefaçon, plagiat, reproduction illicite encourt une poursuite pénale. Contact : [email protected] LIENS Code de la Propriété Intellectuelle. articles L 122. 4 Code de la Propriété Intellectuelle. articles L 335.2- L 335.10 http://www.cfcopies.com/V2/leg/leg_droi.php http://www.culture.gouv.fr/culture/infos-pratiques/droits/protection.htm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
7. PSEUDOLARIX Gordon, Pinetum 292. 1858, Nom. Cons. 金钱松属 Jin Qian Song Shu Chrysolarix H
Flora of China 4: 41–42. 1999. 7. PSEUDOLARIX Gordon, Pinetum 292. 1858, nom. cons. 金钱松属 jin qian song shu Chrysolarix H. E. Moore; Laricopsis Kent. Trees deciduous; trunk monopodial, straight, terete; branches irregularly whorled; branchlets strongly dimorphic: long branchlets with leaves spirally arranged and radially spreading; short branchlets with leaves radially arranged in false whorls of 10–30 (often spirally spread like a discoid star). Leaves green, turning golden yellow before falling in autumn, narrowly oblanceolate-linear, flattened, 1.5–4 mm wide, flexible, stomatal lines abaxial, in 2 bands, separated by midvein, vascular bundle 1, resin canals 2 or 3 (–7), marginal. Pollen cones terminal on short branchlets, borne in umbellate clusters of 10–25, pendulous at maturity; pollen 2-saccate. Seed cones solitary, shortly pedunculate, erect or ± spreading, ovoid-globose, 2-seeded, maturing in 1st year. Seed scales thick, woody, deciduous at maturity. Bracts adnate to seed scales at base and shed together with them at maturity. Seeds with large, backward projecting wing extending beyond scale margin at maturity. Cotyledons 4–7. 2n = 44*. • One species: China. 1. Pseudolarix amabilis (J. Nelson) Rehder, J. Arnold Arbor. 1: 53. 1919. 金钱松 jin qian song Larix amabilis J. Nelson, Pinaceae 84. 1866; Abies kaempferi Lindley; Chrysolarix amabilis (J. Nelson) H. E. Moore; Laricopsis kaempferi (Lindley) Kent; Pseudolarix fortunei Mayr; P. kaempferi Gordon; P. pourtetii Ferré. Trees to 40 m tall; trunk to 3 m d.b.h.; bark gray-brown, rough, scaly, flaking; crown broadly conical; long branchlets initially reddish brown or reddish yellow, glossy, glabrous, becoming yellowish gray, brownish gray, or rarely purplish brown in 2nd or 3rd year, finally gray or dark gray; short branchlets slow growing, bearing dense rings of leaf cushions; winter buds ovoid, scales free at apex. -
Biodiversity Conservation in Botanical Gardens
AgroSMART 2019 International scientific and practical conference ``AgroSMART - Smart solutions for agriculture'' Volume 2019 Conference Paper Biodiversity Conservation in Botanical Gardens: The Collection of Pinaceae Representatives in the Greenhouses of Peter the Great Botanical Garden (BIN RAN) E M Arnautova and M A Yaroslavceva Department of Botanical garden, BIN RAN, Saint-Petersburg, Russia Abstract The work researches the role of botanical gardens in biodiversity conservation. It cites the total number of rare and endangered plants in the greenhouse collection of Peter the Great Botanical garden (BIN RAN). The greenhouse collection of Pinaceae representatives has been analysed, provided with a short description of family, genus and certain species, presented in the collection. The article highlights the importance of Pinaceae for various industries, decorative value of plants of this group, the worth of the pinaceous as having environment-improving properties. In Corresponding Author: the greenhouses there are 37 species of Pinaceae, of 7 geni, all species have a E M Arnautova conservation status: CR -- 2 species, EN -- 3 species, VU- 3 species, NT -- 4 species, LC [email protected] -- 25 species. For most species it is indicated what causes depletion. Most often it is Received: 25 October 2019 the destruction of natural habitats, uncontrolled clearance, insect invasion and diseases. Accepted: 15 November 2019 Published: 25 November 2019 Keywords: biodiversity, botanical gardens, collections of tropical and subtropical plants, Pinaceae plants, conservation status Publishing services provided by Knowledge E E M Arnautova and M A Yaroslavceva. This article is distributed under the terms of the Creative Commons 1. Introduction Attribution License, which permits unrestricted use and Nowadays research of biodiversity is believed to be one of the overarching goals for redistribution provided that the original author and source are the modern world. -
Open As a Single Document
ILLUSTRATIONS Professor Charles Sprague Sargent in the Arnold Arboretum Library -1904, Plate I, opposite p. 30 Flowers and fruits of the hardy orange, Porrcirus tr;f’oliata. Plate II, p. 35 Map showing absolute minimum temperatures in the Northeastern states from 1926-1940. Plate III, p. 47 Map showing an average length for growing season in the Northeast- ern states. Plate IV, p. 49 Map showing the average July temperature in the Northeastern states for the years 1926 to 1940. Plate V, p. 511 Black walnuts. Plate VI, p. 33 Hickory nuts of various types. Plate VII, p. 57 The native rock elm, Ulmu.r thomasi. Plate VIII, p. 69 The European white elm or Russian elm, Lllmus laenis. Plate IX, p.711 Two varieties of the smoothleaf elm, L’lmus carpinjfolia. Plate X, p. 755 Leaf specimens of various elm species. Plate XI, p. 79 111 . ARNOLDIA A continuation of the BULLETIN OF POPULAR INFORMATION of the Arnold Arboretum, Harvard University VOLUME 1 MARCH 14, 1941 NUMBER I A SIMPLE CHANGE IN NAME "Bulletin of Popular Information" has always been an un- OURsatisfactory periodical to cite, because of the form of its title, which reads: "Arnold Arboretum, Harvard University, Bulletin of Popular Information." Moreover, for no very obvious reason, in the twenty-nine years of its publication it has attamed four series, and for clarity it is necessary to cite the series as well as the volume. In- itiated in May, 1911, sixty-three unpaged numbers form the first series, this run closing in November, 1914. In 1915, a new series was commenced with volume one and was continued for twelve years, closing with volume twelve in December, 1926. -
Bgci's Plant Conservation Programme in China
SAFEGUARDING A NATION’S BOTANICAL HERITAGE – BGCI’S PLANT CONSERVATION PROGRAMME IN CHINA Images: Front cover: Rhododendron yunnanense , Jian Chuan, Yunnan province (Image: Joachim Gratzfeld) Inside front cover: Shibao, Jian Chuan, Yunnan province (Image: Joachim Gratzfeld) Title page: Davidia involucrata , Daxiangling Nature Reserve, Yingjing, Sichuan province (Image: Xiangying Wen) Inside back cover: Bretschneidera sinensis , Shimen National Forest Park, Guangdong province (Image: Xie Zuozhang) SAFEGUARDING A NATION’S BOTANICAL HERITAGE – BGCI’S PLANT CONSERVATION PROGRAMME IN CHINA Joachim Gratzfeld and Xiangying Wen June 2010 Botanic Gardens Conservation International One in every five people on the planet is a resident of China But China is not only the world’s most populous country – it is also a nation of superlatives when it comes to floral diversity: with more than 33,000 native, higher plant species, China is thought to be home to about 10% of our planet’s known vascular flora. This botanical treasure trove is under growing pressure from a complex chain of cause and effect of unprecedented magnitude: demographic, socio-economic and climatic changes, habitat conversion and loss, unsustainable use of native species and introduction of exotic ones, together with environmental contamination are rapidly transforming China’s ecosystems. There is a steady rise in the number of plant species that are on the verge of extinction. Great Wall, Badaling, Beijing (Image: Zhang Qingyuan) Botanic Gardens Conservation International (BGCI) therefore seeks to assist China in its endeavours to maintain and conserve the country’s extraordinary botanical heritage and the benefits that this biological diversity provides for human well-being. It is a challenging venture and represents one of BGCI’s core practical conservation programmes. -
Phylogeny and Biogeography of Tsuga (Pinaceae)
Systematic Botany (2008), 33(3): pp. 478–489 © Copyright 2008 by the American Society of Plant Taxonomists Phylogeny and Biogeography of Tsuga (Pinaceae) Inferred from Nuclear Ribosomal ITS and Chloroplast DNA Sequence Data Nathan P. Havill1,6, Christopher S. Campbell2, Thomas F. Vining2,5, Ben LePage3, Randall J. Bayer4, and Michael J. Donoghue1 1Department of Ecology and Evolutionary Biology, Yale University, New Haven, Connecticut 06520-8106 U.S.A 2School of Biology and Ecology, University of Maine, Orono, Maine 04469-5735 U.S.A. 3The Academy of Natural Sciences, 1900 Benjamin Franklin Parkway, Philadelphia, Pennsylvania 19103 U.S.A. 4CSIRO – Division of Plant Industry, Center for Plant Biodiversity Research, GPO 1600, Canberra, ACT 2601 Australia; present address: Department of Biology, University of Memphis, Memphis, Tennesee 38152 U.S.A. 5Present address: Delta Institute of Natural History, 219 Dead River Road, Bowdoin, Maine 04287 U.S.A. 6Author for correspondence ([email protected]) Communicating Editor: Matt Lavin Abstract—Hemlock, Tsuga (Pinaceae), has a disjunct distribution in North America and Asia. To examine the biogeographic history of Tsuga, phylogenetic relationships among multiple accessions of all nine species were inferred using chloroplast DNA sequences and multiple cloned sequences of the nuclear ribosomal ITS region. Analysis of chloroplast and ITS sequences resolve a clade that includes the two western North American species, T. heterophylla and T. mertensiana, and a clade of Asian species within which one of the eastern North American species, T. caroliniana, is nested. The other eastern North American species, T. canadensis, is sister to the Asian clade. Tsuga chinensis from Taiwan did not group with T. -
Cedrus, Keteleeria, Pseudolarix, and Pseudo- Key Words: Abies, Larix
IAWA Journal, Vol. 15 (4), 1994: 399-406 FUSIFORM PARENCHYMA CELLS IN THE YOUNG WOOD OF PINACEAE, AND THEIR DISTINCTION FROM MARGINAL PARENCHYMA by Shuichi Noshiro and Tomoyuki Fujii Wood Anatomy Laboratory, Forestry and Forest Products Research Institute, Tsukuba Norin, P. O. Box 16, Ibaraki 305, Japan Summary Fusiform parenchyma cells found in sev ray tracheids, and the proportion of ray tra eral genera of Pinaceae are described and cheid pit border types. Recently, Anagnost compared with marginal parenchyma. Fusi et al. (1994) restudied all these features using form parenchyma cells are mostly fusiform world-wide sam pIes of Picea and Larix, and in shape, with occasional smooth horizontal confirmed the results of Bartholin (1979) that walls. They form discontinuous tangential ray tracheid pit border types were the most bands in complete or incomplete circ1es in the reliable characteristic. However, because of innermost growth rings of Larix, Abies, and restricted growth in branches, it was difficult Tsuga. Fusiform parenchyma always con to use these stemwood characteristics in iden tains resinous material, and is more conspic tifying branchwoods. uous in branchwoods than in stern woods. Modern branchwood materials gathered Marginal parenchyma cells were observed in for comparative purposes, however, revealed Cedrus, Keteleeria, Pseudolarix, and Pseudo the conspicuous occurrence of resinous paren tsuga as weIl as in Larix, Abies, and Tsuga, chyma cells in the inner growth rings of Larix and very rarely in Picea. Marginal paren and their absence in Picea. Occurrence of chyma cells are scattered along growth ring resinous parenchyma ceHs was also observed boundaries. They are always in strands with in the Quaternary branchwoods, and was used nodular horizontal walls with conspicuous to distinguish Larix branchwoods from Picea simple pits.