Plant Morphology Booklet
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Technical Note 37: Identification, Ecology, Use, and Culture of Sitka
TECHNICAL NOTES _____________________________________________________________________________________________ US DEPT. OF AGRICULTURE NATURAL RESOURCES CONSERVATION SERVICE Portland, OR April 2005 PLANT MATERIALS No. 37 Identification, Ecology, Use and Culture of Sitka Alder Dale C. Darris, Conservation Agronomist, Corvallis Plant Materials Center Introduction Sitka alder [Alnus viridis (Vill.) Lam. & DC. subsp. sinuata (Regel) A.& D. Löve] is a native deciduous shrub or small tree that grows to height of 20 ft, occasionally taller. Although a non-crop species, it has several characteristics useful for reclamation, forestry, and erosion control. The species is known for abundant leaf litter production, the fixation of atmospheric nitrogen in association with Frankia bacteria, and a strong fibrous root system. Where locally abundant, it naturally colonizes landslide chutes, areas of stream scour and deposition, soil slumps, and other drastic disturbances resulting in exposed minerals soils. These characteristics make Sitka alder particularly useful for streambank stabilization and soil building on impoverished sites. In addition, its low height and early slowdown in growth rate makes it potentially more desirable than red alder (Alnus rubra) to interplant with conifers such as Douglas fir (Pseudotsuga menzieii) and lodgepole pine (Pinus contorta) where soil fertility is moderate to low. However, high densities can hinder forest regeneration efforts. The species may also be useful as a fast growing shrub row in field windbreaks. Sitka alder is most abundant at mid to subalpine elevations. Low elevation seed sources (below 100 m) are uncommon but probably provide the best material for reclamation and erosion control projects on valley floors and terraces. Distribution and Identification Sitka alder (Alnus viridis subsp. sinuata) is a native deciduous shrub or small tree that grows to a height of 1-6 m (3-19 ft) in the mountains and 6-12 m (19-37ft) at low elevations. -
The Prosopis Juliflora - Prosopis Pallida Complex: a Monograph
DFID DFID Natural Resources Systems Programme The Prosopis juliflora - Prosopis pallida Complex: A Monograph NM Pasiecznik With contributions from P Felker, PJC Harris, LN Harsh, G Cruz JC Tewari, K Cadoret and LJ Maldonado HDRA - the organic organisation The Prosopis juliflora - Prosopis pallida Complex: A Monograph NM Pasiecznik With contributions from P Felker, PJC Harris, LN Harsh, G Cruz JC Tewari, K Cadoret and LJ Maldonado HDRA Coventry UK 2001 organic organisation i The Prosopis juliflora - Prosopis pallida Complex: A Monograph Correct citation Pasiecznik, N.M., Felker, P., Harris, P.J.C., Harsh, L.N., Cruz, G., Tewari, J.C., Cadoret, K. and Maldonado, L.J. (2001) The Prosopis juliflora - Prosopis pallida Complex: A Monograph. HDRA, Coventry, UK. pp.172. ISBN: 0 905343 30 1 Associated publications Cadoret, K., Pasiecznik, N.M. and Harris, P.J.C. (2000) The Genus Prosopis: A Reference Database (Version 1.0): CD ROM. HDRA, Coventry, UK. ISBN 0 905343 28 X. Tewari, J.C., Harris, P.J.C, Harsh, L.N., Cadoret, K. and Pasiecznik, N.M. (2000) Managing Prosopis juliflora (Vilayati babul): A Technical Manual. CAZRI, Jodhpur, India and HDRA, Coventry, UK. 96p. ISBN 0 905343 27 1. This publication is an output from a research project funded by the United Kingdom Department for International Development (DFID) for the benefit of developing countries. The views expressed are not necessarily those of DFID. (R7295) Forestry Research Programme. Copies of this, and associated publications are available free to people and organisations in countries eligible for UK aid, and at cost price to others. Copyright restrictions exist on the reproduction of all or part of the monograph. -
Invasive Weeds of the Appalachian Region
$10 $10 PB1785 PB1785 Invasive Weeds Invasive Weeds of the of the Appalachian Appalachian Region Region i TABLE OF CONTENTS Acknowledgments……………………………………...i How to use this guide…………………………………ii IPM decision aid………………………………………..1 Invasive weeds Grasses …………………………………………..5 Broadleaves…………………………………….18 Vines………………………………………………35 Shrubs/trees……………………………………48 Parasitic plants………………………………..70 Herbicide chart………………………………………….72 Bibliography……………………………………………..73 Index………………………………………………………..76 AUTHORS Rebecca M. Koepke-Hill, Extension Assistant, The University of Tennessee Gregory R. Armel, Assistant Professor, Extension Specialist for Invasive Weeds, The University of Tennessee Robert J. Richardson, Assistant Professor and Extension Weed Specialist, North Caro- lina State University G. Neil Rhodes, Jr., Professor and Extension Weed Specialist, The University of Ten- nessee ACKNOWLEDGEMENTS The authors would like to thank all the individuals and organizations who have contributed their time, advice, financial support, and photos to the crea- tion of this guide. We would like to specifically thank the USDA, CSREES, and The Southern Region IPM Center for their extensive support of this pro- ject. COVER PHOTO CREDITS ii 1. Wavyleaf basketgrass - Geoffery Mason 2. Bamboo - Shawn Askew 3. Giant hogweed - Antonio DiTommaso 4. Japanese barberry - Leslie Merhoff 5. Mimosa - Becky Koepke-Hill 6. Periwinkle - Dan Tenaglia 7. Porcelainberry - Randy Prostak 8. Cogongrass - James Miller 9. Kudzu - Shawn Askew Photo credit note: Numbers in parenthesis following photo captions refer to the num- bered photographer list on the back cover. HOW TO USE THIS GUIDE Tabs: Blank tabs can be found at the top of each page. These can be custom- ized with pen or marker to best suit your method of organization. Examples: Infestation present On bordering land No concern Uncontrolled Treatment initiated Controlled Large infestation Medium infestation Small infestation Control Methods: Each mechanical control method is represented by an icon. -
Goethe's Plant Morphology: the Seeds of Evolution
JIDRJournalofInterdisciplinaryResearch Goethe’s Plant Morphology: The Seeds of Evolution TANYA KELLEY It has long been debated whether botanist Carl Linnaeus (1707-1778), and the scientific writing of Johann the continuous view of nature, as Wolfgang von Goethe (1749-1832) exemplified in the work of the English provided the seeds for the theory of naturalist Charles Darwin (1809-1882). evolution. Scholars have argued both Although best known for his sides with equal passion. German literary works, such as Faust, Die Leiden biologist and philosopher, Ernst Haeckel des jungen Werther, and Wilhelm (1834-1919) wrote, “Jean and Lamarck Meister, Goethe was also deeply and Wolfgang Goethe stand at the head involved with the sciences. Some of his of all the great philosophers of nature biographers lament that Goethe’s literary who first established a theory of organic productivity was impeded by all the time development, and who are the illustrious he spent pursuing his interests in fellow workers of Darwin.”1 Taking the comparative anatomy, metallurgy, opposite stance was Chancellor of Berlin meteorology, color theory and botany.3 University, Emil du Bois Reymond Goethe himself said that he valued his (1818-1896). Du Bois was embarrassed work as a scientist more than his poetic by Goethe’s forays into science. He work.4 He pursued a wide range of wrote, “Beside the poet, the scientist interests over the course of his 83 years Goethe fades into the background. Let of life. Until the very end of his life he us at long last put him to rest.”2 I argue was vitally interested in science. -
Alnus Glutinosa Common Name
Plant Profiles: HORT 2242 Landscape Plants II Botanical Name: Alnus glutinosa Common Name: European alder, common alder, black alder Family Name: Betulaceae - birch family General Description: Alnus glutinosa is an intermediate size tree that can be grown single stem or clump. It has been a popular plant in the landscape due to its size, shape, winter texture and ability to grow in diverse landscape settings. European black alder is especially useful for wet sites and poor infertile sites as it has the ability to fix nitrogen in nodules on its root system. However, it is a non-native tree that has escaped cultivation and can now be found along rivers and other natural habitats in the Chicago area. According to The Morton Arboretum, this plant is invasive and should not be planted. Zone: 3-7 Resources Consulted: "Black alder." Trees & Plants. Morton Arboretum, 2013. Web. 26 Feb. 2014. Dirr, Michael A. Manual of Woody Landscape Plants: Their Identification, Ornamental Characteristics, Culture, Propagation and Uses. Champaign: Stipes, 2009. Print. "The PLANTS Database." USDA, NRCS. National Plant Data Team, Greensboro, NC 27401-4901 USA, 2014. Web. 17 Mar. 2014. Swink, Floyd, and Gerould Wilhelm. Plants of the Chicago Region. Indianapolis: Indiana Academy of Science, 1994. Print. Creator: Julia Fitzpatrick-Cooper, Professor, College of DuPage Creation Date: 2014 Keywords/Tags: Alnus glutinosa, European alder, black alder, deciduous, tree Whole plant/Habit: Description: Alnus glutinosa is a pyramidal tree. When grown single stem it has an almost formal pyramidal shape. However, it is frequently multi- stemmed (clump-form) with a less formal, weak, narrow, pyramidal shape. -
100 Cold Hardy Trees, Perennials, and Shrubs for Kittitas County
100 Cold Hardy Trees, Perennials, and Shrubs for Kittitas County Prepared By Hilary Foss, Master Gardener Coordinator Patrice Andersen, Master Gardener Mary Vathauer, Master Gardener 100 Cold Hardy Trees, Perennials, and Shrubs for Kittitas County Gardeners in Kittitas County face unique challenges. Cold winters and hot, dry summers, and lots of wind create a tough gardening climate. Additionally, our county contains a wide range of eco-systems, with varying soils, soil pH, rainfall, and plant communities. At higher elevations such as Cle Elum (1,930 feet), the average growing season is 90 to 120 days with last frosts in late May (approximately May 24 th ) and first frosts in the middle of September (approximately September 11th ). Cle Elum receives about 22” of rain on average. At lower elevations such as Ellensburg, conditions are much drier and frost-free days are longer. The average growing season in Ellensburg is about 120 days with last frosts in early May (May 11 th ) and first frosts around the end of September (approximately September 25 th ). Kittitas County is rated at USDA Zone 5 (-20 °F. minimum). Our tough climate with varying conditions can be baffling to first time gardeners, who are new to the area. A frequent question at our Master Gardener plant diagnostic clinic is “What can I grow here in Kittitas County?” This brochure is designed to help answer that question, listing trees, shrubs, and perennials that are suitable for this area. Table of Contents 10 Hardy Shade Trees .............................................................................................................................................................................................................................2-3 -
Synthetic Conversion of Leaf Chloroplasts Into Carotenoid-Rich Plastids Reveals Mechanistic Basis of Natural Chromoplast Development
Synthetic conversion of leaf chloroplasts into carotenoid-rich plastids reveals mechanistic basis of natural chromoplast development Briardo Llorentea,b,c,1, Salvador Torres-Montillaa, Luca Morellia, Igor Florez-Sarasaa, José Tomás Matusa,d, Miguel Ezquerroa, Lucio D’Andreaa,e, Fakhreddine Houhouf, Eszter Majerf, Belén Picóg, Jaime Cebollag, Adrian Troncosoh, Alisdair R. Ferniee, José-Antonio Daròsf, and Manuel Rodriguez-Concepciona,f,1 aCentre for Research in Agricultural Genomics (CRAG) CSIC-IRTA-UAB-UB, Campus UAB Bellaterra, 08193 Barcelona, Spain; bARC Center of Excellence in Synthetic Biology, Department of Molecular Sciences, Macquarie University, Sydney NSW 2109, Australia; cCSIRO Synthetic Biology Future Science Platform, Sydney NSW 2109, Australia; dInstitute for Integrative Systems Biology (I2SysBio), Universitat de Valencia-CSIC, 46908 Paterna, Valencia, Spain; eMax-Planck-Institut für Molekulare Pflanzenphysiologie, 14476 Potsdam-Golm, Germany; fInstituto de Biología Molecular y Celular de Plantas, CSIC-Universitat Politècnica de València, 46022 Valencia, Spain; gInstituto de Conservación y Mejora de la Agrodiversidad, Universitat Politècnica de València, 46022 Valencia, Spain; and hSorbonne Universités, Université de Technologie de Compiègne, Génie Enzymatique et Cellulaire, UMR-CNRS 7025, CS 60319, 60203 Compiègne Cedex, France Edited by Krishna K. Niyogi, University of California, Berkeley, CA, and approved July 29, 2020 (received for review March 9, 2020) Plastids, the defining organelles of plant cells, undergo physiological chromoplasts but into a completely different type of plastids and morphological changes to fulfill distinct biological functions. In named gerontoplasts (1, 2). particular, the differentiation of chloroplasts into chromoplasts The most prominent changes during chloroplast-to-chromo- results in an enhanced storage capacity for carotenoids with indus- plast differentiation are the reorganization of the internal plastid trial and nutritional value such as beta-carotene (provitamin A). -
Alnus P. Mill
A Betulaceae—Birch family Alnus P. Mill. alder Constance A. Harrington, Leslie Chandler Brodie, Dean S. DeBell, and C. S. Schopmeyer Dr. Harrington and Ms. Brodie are foresters on the silviculture research team at the USDA Forest Service’s Pacific Northwest Research Station, Olympia,Washington; Dr. DeBell retired from the USDA Forest Service’s Pacific Northwest Research Station; Dr. Schopmeyer (deceased) was the technical coordinator of the previous manual Growth habit and occurrence. Alder—the genus (Tarrant and Trappe 1971). Alders also have been planted for Alnus—includes about 30 species of deciduous trees and wildlife food and cover (Liscinsky 1965) and for ornamental shrubs occurring in North America, Europe, and Asia and in use. European and red alders have been considered for use the Andes Mountains of Peru and Bolivia. Most alders are in biomass plantings for energy (Gillespie and Pope 1994) tolerant of moist sites and thus are commonly found along and are considered excellent firewood. In recent years, har streams, rivers, and lakes and on poorly drained soils; in vest and utilization of red alder has expanded greatly on the addition, some species occur on steep slopes and at high ele Pacific Coast of North America, where the species is used vations. The principal species found in North America are for paper products, pallets, plywood, paneling, furniture, listed in table 1. Many changes in the taxonomy of alder veneer, and cabinetry (Harrington 1984; Plank and Willits have been made over the years; in this summary, species are 1994). Red alder is also used as a fuel for smoking or curing referred to by their currently accepted names although in salmon and other seafood and its bark is used to make a red many cases the information was published originally under or orange dye (Pojar and MacKinnon 1994). -
Research Advances on Leaf and Wood Anatomy of Woody Species
rch: O ea pe es n A R t c s c Rodriguez et al., Forest Res 2016, 5:3 e e r s o s Forest Research F DOI: 10.4172/2168-9776.1000183 Open Access ISSN: 2168-9776 Research Article Open Access Research Advances on Leaf and Wood Anatomy of Woody Species of a Tamaulipan Thorn Scrub Forest and its Significance in Taxonomy and Drought Resistance Rodriguez HG1*, Maiti R1 and Kumari A2 1Universidad Autónoma de Nuevo León, Facultad de Ciencias Forestales, Carr. Nac. No. 85 Km. 45, Linares, Nuevo León 67700, México 2Plant Physiology, Agricultural College, Professor Jaya Shankar Telangana State Agricultural University, Polasa, Jagtial, Karimnagar, Telangana, India Abstract The present paper make a synthesis of a comparative leaf anatomy including leaf surface, leaf lamina, petiole and venation as well as wood anatomy of 30 woody species of a Tamaulipan Thorn Scrub, Northeastern Mexico. The results showed a large variability in anatomical traits of both leaf and wood anatomy. The variations of these anatomical traits could be effectively used in taxonomic delimitation of the species and adaptation of the species to xeric environments. For example the absence or low frequency of stomata on leaf surface, the presence of long palisade cells, and presence of narrow xylem vessels in the wood could be related to adaptation of the species to drought. Besides the species with dense venation and petiole with thick collenchyma and sclerenchyma and large vascular bundle could be well adapted to xeric environments. It is suggested that a comprehensive consideration of leaf anatomy (leaf surface, lamina, petiole and venation) and wood anatomy should be used as a basis of taxonomy and drought resistance. -
Effects of Nitrogen Dioxide on Biochemical Responses in 41 Garden Plants
plants Article Effects of Nitrogen Dioxide on Biochemical Responses in 41 Garden Plants Qianqian Sheng 1 and Zunling Zhu 1,2,* 1 College of Landscape Architecture, Nanjing Forestry University, Nanjing 210037, China; [email protected] 2 College of Art & Design, Nanjing Forestry University, Nanjing 210037, China * Correspondence: [email protected]; Tel.: +86-25-6822-4603 Received: 11 December 2018; Accepted: 12 February 2019; Published: 16 February 2019 Abstract: Nitrogen dioxide (NO2) at a high concentration is among the most common and harmful air pollutants. The present study aimed to explore the physiological responses of plants exposed to NO2. A total of 41 plants were classified into 13 functional groups according to the Angiosperm Phylogeny Group classification system. The plants were exposed to 6 µL/L NO2 in an open-top glass chamber. The physiological parameters (chlorophyll (Chl) content, peroxidase (POD) activity, and soluble protein and malondialdehyde (MDA) concentrations) and leaf mineral ion contents (nitrogen (N+), phosphorus (P+), potassium (K+), calcium (Ca2+), magnesium (Mg2+), manganese 2+ 2+ (Mn ), and zinc (Zn )) of 41 garden plants were measured. After NO2 exposure, the plants were subsequently transferred to a natural environment for a 30-d recovery to determine whether they could recover naturally and resume normal growth. The results showed that NO2 polluted the plants and that NO2 exposure affected leaf Chl contents in most functional groups. Increases in both POD activity and soluble protein and MDA concentrations as well as changes in mineral ion concentrations could act as signals for inducing defense responses. Furthermore, antioxidant status played an important role in plant protection against NO2-induced oxidative damage. -
Ferns of the National Forests in Alaska
Ferns of the National Forests in Alaska United States Forest Service R10-RG-182 Department of Alaska Region June 2010 Agriculture Ferns abound in Alaska’s two national forests, the Chugach and the Tongass, which are situated on the southcentral and southeastern coast respectively. These forests contain myriad habitats where ferns thrive. Most showy are the ferns occupying the forest floor of temperate rainforest habitats. However, ferns grow in nearly all non-forested habitats such as beach meadows, wet meadows, alpine meadows, high alpine, and talus slopes. The cool, wet climate highly influenced by the Pacific Ocean creates ideal growing conditions for ferns. In the past, ferns had been loosely grouped with other spore-bearing vascular plants, often called “fern allies.” Recent genetic studies reveal surprises about the relationships among ferns and fern allies. First, ferns appear to be closely related to horsetails; in fact these plants are now grouped as ferns. Second, plants commonly called fern allies (club-mosses, spike-mosses and quillworts) are not at all related to the ferns. General relationships among members of the plant kingdom are shown in the diagram below. Ferns & Horsetails Flowering Plants Conifers Club-mosses, Spike-mosses & Quillworts Mosses & Liverworts Thirty of the fifty-four ferns and horsetails known to grow in Alaska’s national forests are described and pictured in this brochure. They are arranged in the same order as listed in the fern checklist presented on pages 26 and 27. 2 Midrib Blade Pinnule(s) Frond (leaf) Pinna Petiole (leaf stalk) Parts of a fern frond, northern wood fern (p. -
The Vascular System of Monocotyledonous Stems Author(S): Martin H
The Vascular System of Monocotyledonous Stems Author(s): Martin H. Zimmermann and P. B. Tomlinson Source: Botanical Gazette, Vol. 133, No. 2 (Jun., 1972), pp. 141-155 Published by: The University of Chicago Press Stable URL: http://www.jstor.org/stable/2473813 . Accessed: 30/08/2011 15:50 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 Botanical Gazette. http://www.jstor.org 1972] McCONNELL& STRUCKMEYER ALAR AND BORON-DEFICIENTTAGETES 141 tomato, turnip and cotton to variations in boron nutri- Further investigationson the relation of photoperiodto tion. II. Anatomical responses. BOT.GAZ. 118:53-71. the boron requirementsof plants. BOT.GAZ. 109:237-249. REED, D. J., T. C. MOORE, and J. D. ANDERSON. 1965. Plant WATANABE,R., W. CHORNEY,J. SKOK,and S. H. WENDER growth retardant B-995: a possible mode of action. 1964. Effect of boron deficiency on polyphenol produc- Science 148: 1469-1471. tion in the sunflower.Phytochemistry 3:391-393. SKOK, J. 1957. Relationships of boron nutrition to radio- ZEEVAART,J. A. D. 1966. Inhibition of stem growth and sensitivity of sunflower plants.