Environmental and Anthropogenic Pressures on Geophytes of Iran and the Possible Protection Strategies: a Review
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Liliaceae S.L. (Lily Family)
Liliaceae s.l. (Lily family) Photo: Ben Legler Photo: Hannah Marx Photo: Hannah Marx Lilium columbianum Xerophyllum tenax Trillium ovatum Liliaceae s.l. (Lily family) Photo: Yaowu Yuan Fritillaria lanceolata Ref.1 Textbook DVD KRR&DLN Erythronium americanum Allium vineale Liliaceae s.l. (Lily family) Herbs; Ref.2 Stems often modified as underground rhizomes, corms, or bulbs; Flowers actinomorphic; 3 sepals and 3 petals or 6 tepals, 6 stamens, 3 carpels, ovary superior (or inferior). Tulipa gesneriana Liliaceae s.l. (Lily family) “Liliaceae” s.l. (sensu lato: “in the broad sense”) - Lily family; 288 genera/4950 species, including Lilium, Allium, Trillium, Tulipa; This family is treated in a very broad sense in this class, as in the Flora of the Pacific Northwest. The “Liliaceae” s.l. taught in this class is not monophyletic. It is apparent now that the family should be treated in a narrower sense and some of the members should form their own families. Judd et al. recognize 15+ families: Agavaceae, Alliaceae, Amarylidaceae, Asparagaceae, Asphodelaceae, Colchicaceae, Dracaenaceae (Nolinaceae), Hyacinthaceae, Liliaceae, Melanthiaceae, Ruscaceae, Smilacaceae, Themidaceae, Trilliaceae, Uvulariaceae and more!!! (see web reading “Consider the Lilies”) Iridaceae (Iris family) Photo: Hannah Marx Photo: Hannah Marx Iris pseudacorus Iridaceae (Iris family) Photo: Yaowu Yuan Photo: Yaowu Yuan Sisyrinchium douglasii Sisyrinchium sp. Iridaceae (Iris family) Iridaceae - 78 genera/1750 species, Including Iris, Gladiolus, Sisyrinchium. Herbs, aquatic or terrestrial; Underground stems as rhizomes, bulbs, or corms; Leaves alternate, 2-ranked and equitant Ref.3 (oriented edgewise to the stem; Gladiolus italicus Flowers actinomorphic or zygomorphic; 3 sepals and 3 petals or 6 tepals; Stamens 3; Ovary of 3 fused carpels, inferior. -
Bulb Dormancy in Vitro—Fritillaria Meleagris: Initiation, Release and Physiological Parameters
plants Review Bulb Dormancy In Vitro—Fritillaria meleagris: Initiation, Release and Physiological Parameters Marija Markovi´c*, Milana Trifunovi´cMomˇcilov , Branka Uzelac , Sladana¯ Jevremovi´c and Angelina Suboti´c Department of Plant Physiology, Institute for Biological Research “Siniša Stankovi´c“—NationalInstitute of the Republic of Serbia, University of Belgrade, Bulevar Despota Stefana 142, 11060 Belgrade, Serbia; [email protected] (M.T.M.); [email protected] (B.U.); [email protected] (S.J.); [email protected] (A.S.) * Correspondence: [email protected] Abstract: In ornamental geophytes, conventional vegetative propagation is not economically feasible due to very slow development and ineffective methods. It can take several years until a new plant is formed and commercial profitability is achieved. Therefore, micropropagation techniques have been developed to increase the multiplication rate and thus shorten the multiplication and regeneration period. The majority of these techniques rely on the formation of new bulbs and their sprouting. Dormancy is one of the main limiting factors to speed up multiplication in vitro. Bulbous species have a period of bulb dormancy which enables them to survive unfavorable natural conditions. Bulbs grown in vitro also exhibit dormancy, which has to be overcome in order to allow sprouting of bulbs in the next vegetation period. During the period of dormancy, numerous physiological processes occur, many of which have not been elucidated yet. Understanding the process of dormancy will allow us to speed up and improve breeding of geophytes and thereby achieve economic profitability, which is very important for horticulture. This review focuses on recent findings in the area of Citation: Markovi´c,M.; Momˇcilov, bulb dormancy initiation and release in fritillaries, with particular emphasis on the effect of plant M.T.; Uzelac, B.; Jevremovi´c,S.; growth regulators and low-temperature pretreatment on dormancy release in relation to induction of Suboti´c,A. -
FLOWER DEVELOPMENT and SENESCENCE in Ranunculus Asiaticus L
Journal of Fruit and Ornamental Plant Research Vol. 19(2) 2011: 123-131 FLOWER DEVELOPMENT AND SENESCENCE IN Ranunculus asiaticus L. Waseem Shahri and Inayatullah Tahir Department of Botany, University of Kashmir, Srinagar- 190006, INDIA Running title: Petal Senescence e-mail: [email protected] (Received November 24, 2010/Accepted July 7, 2011) ABSTRACT Flower development of Ranunculus asiaticus L. growing in the University Bo- tanic Garden was divided into six stages (I – VI): tight bud stage (I), loose bud stage (II), half open stage (III), open flower stage (IV), partially senescent stage (V) and senescent stage (VI). The average life span of an individual flower after it is fully open is about 5 days. Membrane permeability of sepal tissues estimated as electrical conductivity of ion leachates (µS), increased as the development proceeded through various stages. The content of sugars in the petal tissues increased during the flower opening period and then declined during senescence. The soluble proteins registered a consistent decrease with the simultaneous increase in specific protease activity and α-amino acid content during different stages of flower development and senescence. The content of total phenols registered an initial increase as the flowers opened, and then declined during senescence. Keywords: α-amino acids, flower senescence, membrane permeability, protease ac- tivity, soluble proteins, Ranunculus asiaticus, tissue constituents INTRODUCTION in gene expression and requires ac- tive gene transcription and protein Senescence comprises those proc- translation (Yamada et al., 2003; esses that follow physiological matur- Hoeberichts et al., 2005; Jones, ity leading to the death of a whole 2008). Flower petals are ideal tissues plant, organ or tissue, at the macro- for cell death studies as they are scopic level as well as microscopic short lived. -
Karyological Studies of Fritillaria (Liliaceae) Species from Iran
© 2016 The Japan Mendel Society Cytologia 81(2): 133–141 Karyological Studies of Fritillaria (Liliaceae) Species from Iran Marzieh Ahmadi-Roshan1, Ghasem Karimzadeh1*, Alireza Babaei2 and Hadi Jafari2 1 Department of Plant Breeding and Biotechnology, Faculty of Agriculture, Tarbiat Modares University, Tehran P. O. Box 14115–336, Iran 2 Department of Horticultural Sciences, Faculty of Agriculture, Tarbiat Modares University, Tehran, Iran Received September 26, 2015; accepted March 14, 2016 Summary Five species (13 ecotypes) belonging to three subgenera of ornamental-medicinal Iranian Fritillaria were karyotypically studied, using a standard squash technique. All species were diploid (2n=2x=24) having mean chromosome lengths of 15.8 µm (15.2–16.7 µm). Their satellites varied in number (1–3 pairs) and in size (1.2–2.6 µm), mostly being located on long arms. Four chromosome types (“m”, “sm”, “st”, “T”) formed 10 dif- ferent karyotype formulas: “T” type chromosome is reported for the first time in most species (with the exception of S4, Fritillaria. reuteri Boissi). ANOVA confirmed significant intra- and inter-specific chromosomal variation across the Iranian Fritillaria species. Twelve different methods were used to assess the degree of karyotype asymmetry. Among those, one qualitative parameter (Stebbins classification) and eight quantitative (CVTL, DI, A1 & A2, AI, A, AsK%, MCA, CVCI) parameters verified that S2 (F. gibbosa Boiss.) and S5 (F. zagrica Stapf.) species represented the most asymmetrical and symmetrical karyotypes, respectively. Key words Fritillaria, Cytogenetics, New chromosome type, Karyotype, Iran. The name Fritillaria is likely based on the word “fri- Fritillaria subgenus is morphologically classified into six tullus” which means a cup in Latin (Ulug et al. -
Postharvest Storage and Handling of Ranunculus Asiaticus Dried Tuberous Roots
POSTHARVEST STORAGE AND HANDLING OF RANUNCULUS ASIATICUS DRIED TUBEROUS ROOTS A Dissertation Presented to the Faculty of the Graduate School of Cornell University In Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy by Christopher Brian Cerveny January 2011 © 2011 Christopher Brian Cerveny POSTHARVEST STORAGE AND HANDLING OF RANUNCULUS ASIATICUS DRIED TUBEROUS ROOTS Christopher B. Cerveny, Ph. D. Cornell University 2011 Ranunculus asiaticus is an ornamental flowering plant with potential to be more widely used by the floriculture industry. Unfortunately, growers are faced with many challenges when producing these plants from their dry tuberous roots following storage; including poor sprouting, non-uniform growth, disease issues upon planting, as well as inconsistent cultural recommendations and lack of proper storage and handling protocols. Several experiments were conducted to determine the influence of temperature and relative humidity during storage on growth and quality of R. asiaticus plants. From our experiments it can be concluded that R. asiaticus tubers store best under low relative humidity and cool temperatures (above freezing). Also important from a storage perspective, unlike other flower bulbs, we show that R. asiaticus tuberous roots are not susceptible to ethylene damage while in the dry state. Prior to planting, tubers should be submerged in room-temperature water at around 20 oC, for 24 h, and then provided a fungicide treatment. We have shown that proper hydration temperature for R. asiaticus tuberous roots is critical for optimal growth. By following the protocol generated from our experiments, many of the production challenges associated with R. asiaticus tuberous roots may be avoided. -
Verticillium Wilt of Vegetables and Herbaceous Ornamentals
Dr. Sharon M. Douglas Department of Plant Pathology and Ecology The Connecticut Agricultural Experiment Station 123 Huntington Street, P. O. Box 1106 New Haven, CT 06504 Phone: (203) 974-8601 Fax: (203) 974-8502 Founded in 1875 Email: [email protected] Putting science to work for society Website: www.ct.gov/caes VERTICILLIUM WILT OF VEGETABLES AND HERBACEOUS ORNAMENTALS Verticillium wilt is a disease of over 300 SYMPTOMS AND DISEASE species throughout the United States. This DEVELOPMENT: includes a wide variety of vegetables and Symptoms of Verticillium wilt vary by host herbaceous ornamentals. Tomatoes, and environmental conditions. In many eggplants, peppers, potatoes, dahlia, cases, symptoms do not develop until the impatiens, and snapdragon are among the plant is bearing flowers or fruit or after hosts of this disease. Plants weakened by periods of stressful hot, dry weather. Older root damage from drought, waterlogged leaves are usually the first to develop soils, and other environmental stresses are symptoms, which include yellowing, thought to be more prone to infection. wilting, and eventually dying and dropping from the plant. Infected leaves can also Since Verticillium wilt is a common disease, develop pale yellow blotches on the lower breeding programs have contributed many leaves (Figure 1) and necrotic, V-shaped varieties or cultivars of plants with genetic lesions at the tips of the leaves. resistance—this has significantly reduced the prevalence of this disease on many plants, especially on vegetables. However, the recent interest in planting “heirloom” varieties, which do not carry resistance genes, has resulted in increased incidence of Verticillium wilt on these hosts. -
Introduction to Common Native & Invasive Freshwater Plants in Alaska
Introduction to Common Native & Potential Invasive Freshwater Plants in Alaska Cover photographs by (top to bottom, left to right): Tara Chestnut/Hannah E. Anderson, Jamie Fenneman, Vanessa Morgan, Dana Visalli, Jamie Fenneman, Lynda K. Moore and Denny Lassuy. Introduction to Common Native & Potential Invasive Freshwater Plants in Alaska This document is based on An Aquatic Plant Identification Manual for Washington’s Freshwater Plants, which was modified with permission from the Washington State Department of Ecology, by the Center for Lakes and Reservoirs at Portland State University for Alaska Department of Fish and Game US Fish & Wildlife Service - Coastal Program US Fish & Wildlife Service - Aquatic Invasive Species Program December 2009 TABLE OF CONTENTS TABLE OF CONTENTS Acknowledgments ............................................................................ x Introduction Overview ............................................................................. xvi How to Use This Manual .................................................... xvi Categories of Special Interest Imperiled, Rare and Uncommon Aquatic Species ..................... xx Indigenous Peoples Use of Aquatic Plants .............................. xxi Invasive Aquatic Plants Impacts ................................................................................. xxi Vectors ................................................................................. xxii Prevention Tips .................................................... xxii Early Detection and Reporting -
Fall 2013 NARGS
Rock Garden uar terly � Fall 2013 NARGS to ADVERtISE IN thE QuARtERly CoNtACt [email protected] Let me know what yo think A recent issue of a chapter newsletter had an item entitled “News from NARGS”. There were comments on various issues related to the new NARGS website, not all complimentary, and then it turned to the Quarterly online and raised some points about which I would be very pleased to have your views. “The good news is that all the Quarterlies are online and can easily be dowloaded. The older issues are easy to read except for some rather pale type but this may be the result of scanning. There is amazing information in these older issues. The last three years of the Quarterly are also online but you must be a member to read them. These last issues are on Allen Press’s BrightCopy and I find them harder to read than a pdf file. Also the last issue of the Quarterly has 60 extra pages only available online. Personally I find this objectionable as I prefer all my content in a printed bulletin.” This raises two points: Readability of BrightCopy issues versus PDF issues Do you find the BrightCopy issues as good as the PDF issues? Inclusion of extra material in online editions only. Do you object to having extra material in the online edition which can not be included in the printed edition? Please take a moment to email me with your views Malcolm McGregor <[email protected]> CONTRIBUTORS All illustrations are by the authors of articles unless otherwise stated. -
Asiatischer Hahnenfuß
Asiatischer Hahnenfuß Der Asiatische Hahnenfuß (Ranunculus asiaticus), dessen Gartenformen auch Floristen-Ranunkel, Riesenranunkel Asiatischer Hahnenfuß oder Topfranunkel genannt werden, ist eine Pflanzenart aus der Gattung Hahnenfuß (Ranunculus) in der Familie der Hahnenfußgewächse (Ranunculaceae). Sie wird als Zierpflanze in Parks und Gärten sowie als Schnittblume verwendet. Inhaltsverzeichnis Beschreibung Systematik und Verbreitung Kultivierung Einzelnachweise Weblinks Beschreibung Der Asiatische Hahnenfuß wächst als ausdauernde krautige Pflanze, die Wuchshöhen von bis zu 30 Zentimetern erreicht. Dieser Geophyt bildet Speicherwurzeln als Ranunculus asiaticus Überdauerungsorgane und Rhizome.[1] Der Stängel ist nur Wildform am Naturstandort spärlich verzweigt.[2] Die wechselständigen[1] Laubblätter sind unterschiedlich geformt: Die grundständigen Systematik Laubblätter sind oft ungeteilt, doch die meisten Laubblätter Ordnung: Hahnenfußartige sind geteilt, je weiter oben im Stängel, umso schmäler.[2] (Ranunculales) Der Blattrand ist gezähnt bis gesägt.[1] Familie: Hahnenfußgewächse (Ranunculaceae) Die Blütezeit liegt im Frühling. Die zwittrigen Blüten sind Unterfamilie: Ranunculoideae [1] radiärsymmetrisch. Es sind fünf bis sieben leuchtend Tribus: Ranunculeae gefärbte Blütenhüllblätter vorhanden. Die Blütenfarben Gattung: Hahnenfuß (Ranunculus) reichen von weiß über cremefarben bis gelb, orange bis lachsfarben nach karminrot und von rosafarben bis Art: Asiatischer Hahnenfuß purpurrot; sie können einfarbig oder mehrfarbig sein. Die Wissenschaftlicher -
Size Variations of Flowering Characters in Arum Italicum (Araceae)
M. GIBERNAU,]. ALBRE, 2008 101 Size Variations of Flowering Characters in Arum italicum (Araceae) Marc Gibernau· and Jerome Albre Universite Paul Sabatier Laboratoire d'Evolution & Diversite Biologique (UMR 5174) Bat.4R3-B2 31062 Toulouse cedex 9 France *e-mail: [email protected] ABSTRACT INTRODUCTION In Arum, bigger individuals should An extreme form of flowering character proportionally invest more in the female variations according to the size is gender function (number or weight of female modification, which occurs in several flowers) than the male. The aim of this species of Arisaema (Clay, 1993). Individ paper is to quantify variations in repro ual plant gender changes from pure male, ductive characters (size of the spadix when small, to monoecious (A. dracon parts, number of inflorescences) in rela tium) or pure female (A. ringens) when tion to plant and inflorescence sizes. The large (Gusman & Gusman, 2003). This appendix represents 44% of the spadix gender change is reversible, damaged length. The female zone length represents female individuals will flower as male the 16.5% of the spadix length and is much following year (Lovett Doust & Cavers, longer than the male zone (6%). Moreover 1982). These changes are related to change these three spadix zones increase with in plant size and are explained by the plant vigour indicating an increasing size-advantage model. The size-advantage investment into reproduction and pollina model postulates a sex change when an tor attraction. It appears that the length of increase in body size is related to differen appendix increased proportionally more tial abilities to produce or sire offspring than the lengths of the fertile zones. -
Indigenous Plants of Bendigo
Produced by Indigenous Plants of Bendigo Indigenous Plants of Bendigo PMS 1807 RED PMS 432 GREY PMS 142 GOLD A Gardener’s Guide to Growing and Protecting Local Plants 3rd Edition 9 © Copyright City of Greater Bendigo and Bendigo Native Plant Group Inc. This work is Copyright. Apart from any use permitted under the Copyright Act 1968, no part may be reproduced by any process without prior written permission from the City of Greater Bendigo. First Published 2004 Second Edition 2007 Third Edition 2013 Printed by Bendigo Modern Press: www.bmp.com.au This book is also available on the City of Greater Bendigo website: www.bendigo.vic.gov.au Printed on 100% recycled paper. Disclaimer “The information contained in this publication is of a general nature only. This publication is not intended to provide a definitive analysis, or discussion, on each issue canvassed. While the Committee/Council believes the information contained herein is correct, it does not accept any liability whatsoever/howsoever arising from reliance on this publication. Therefore, readers should make their own enquiries, and conduct their own investigations, concerning every issue canvassed herein.” Front cover - Clockwise from centre top: Bendigo Wax-flower (Pam Sheean), Hoary Sunray (Marilyn Sprague), Red Ironbark (Pam Sheean), Green Mallee (Anthony Sheean), Whirrakee Wattle (Anthony Sheean). Table of contents Acknowledgements ...............................................2 Foreword..........................................................3 Introduction.......................................................4 -
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.