Gladiolus Rust: a New Threat
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Summary of Offerings in the PBS Bulb Exchange, Dec 2012- Nov 2019
Summary of offerings in the PBS Bulb Exchange, Dec 2012- Nov 2019 3841 Number of items in BX 301 thru BX 463 1815 Number of unique text strings used as taxa 990 Taxa offered as bulbs 1056 Taxa offered as seeds 308 Number of genera This does not include the SXs. Top 20 Most Oft Listed: BULBS Times listed SEEDS Times listed Oxalis obtusa 53 Zephyranthes primulina 20 Oxalis flava 36 Rhodophiala bifida 14 Oxalis hirta 25 Habranthus tubispathus 13 Oxalis bowiei 22 Moraea villosa 13 Ferraria crispa 20 Veltheimia bracteata 13 Oxalis sp. 20 Clivia miniata 12 Oxalis purpurea 18 Zephyranthes drummondii 12 Lachenalia mutabilis 17 Zephyranthes reginae 11 Moraea sp. 17 Amaryllis belladonna 10 Amaryllis belladonna 14 Calochortus venustus 10 Oxalis luteola 14 Zephyranthes fosteri 10 Albuca sp. 13 Calochortus luteus 9 Moraea villosa 13 Crinum bulbispermum 9 Oxalis caprina 13 Habranthus robustus 9 Oxalis imbricata 12 Haemanthus albiflos 9 Oxalis namaquana 12 Nerine bowdenii 9 Oxalis engleriana 11 Cyclamen graecum 8 Oxalis melanosticta 'Ken Aslet'11 Fritillaria affinis 8 Moraea ciliata 10 Habranthus brachyandrus 8 Oxalis commutata 10 Zephyranthes 'Pink Beauty' 8 Summary of offerings in the PBS Bulb Exchange, Dec 2012- Nov 2019 Most taxa specify to species level. 34 taxa were listed as Genus sp. for bulbs 23 taxa were listed as Genus sp. for seeds 141 taxa were listed with quoted 'Variety' Top 20 Most often listed Genera BULBS SEEDS Genus N items BXs Genus N items BXs Oxalis 450 64 Zephyranthes 202 35 Lachenalia 125 47 Calochortus 94 15 Moraea 99 31 Moraea -
The Taxonomic Status of Gladiolus Illyricus (Iridaceae) in Britain
The Taxonomic Status of Gladiolus illyricus (Iridaceae) in Britain Aeron Buchanan Supervisor: Fred Rumsey, Natural History Museum, London A thesis submitted in partial fulfilment of the requirements for the degree of Master of Science of Imperial College, London Abstract First noticed officially in Britain in 1855, Gladiolus illyricus (Koch) presents an interesting taxonomic and biogeographical challenge: whether or not this isolated northern population should be recognized as a separate sub-species. Fundamental conservation issues rest on the outcome. Here, the investigation into the relationship of the G. illyricus plants of the New Forest, Hampshire, to Gladiolus species across Europe, northern Africa and the middle east is initiated. Two chloroplast regions, one in trnL–trnF and the other across psbA–trnH have been sequenced for 42 speci- mens of G. illyricus, G. communis, G. italicus, G. atroviolaceus, G. triphyllos and G. anatolicus. Phylogenetic and biogeographical treatments support the notion of an east–west genetic gradation along the Mediterranean. Iberia particularly appears as a zone of high hybridization potential and the source of the New Forest population. Alignment with sequences obtained from GenBank give strong support to the classic taxonomy of Gladiolus being monophyletic in its sub-family, Ixioideae. Comments on these chloroplast regions for barcoding are also given. In conclusion, the genetic localization of Britain’s G. illyricus population as an extremity haplotype suggests that it could well deserve sub-species status. Contents 1 Introduction 2 2 Background 4 3 Materials and Methods 8 4 Results and Discussion 15 5 Conclusions 26 Appendices 28 References 56 1. Introduction G. illyricus in Britain Figure 1: G. -
Flowering of Watsonia Laccata As Influenced by Corm Storage and Forcing Temperatures ⁎ J.K
Available online at www.sciencedirect.com South African Journal of Botany 77 (2011) 631–637 www.elsevier.com/locate/sajb Flowering of Watsonia laccata as influenced by corm storage and forcing temperatures ⁎ J.K. Suh a, , J.H. Kim a, A.K. Lee a, M.S. Roh b a Dankook University, College of Bio-Resources Science, Department of Environmental Horticulture, Cheonan, Chungnam 330-714, Republic of Korea b US Department of Agriculture, Agricultural Research Service, National Arboretum, Floral and Nursery Plants Research Unit, Beltsville MD 20705, USA Received 24 March 2010; received in revised form 28 November 2010; accepted 22 December 2010 Abstract The genus Watsonia, belonging to the family Iridaceae, is comprised of about 50 species including W. laccata (Jacquin) Ker Gawler that flowers from September to November following low temperature and winter rainfall. Therefore, we hypothesized that flowering would be favored by forcing at low greenhouse temperatures. Using clonal W. laccata corms, four experiments were designed to investigate the effect of temperatures during corm storage, forcing, and their interaction on growth and flowering. Corm formation is favored by growing plants at 18°– 20°/15°–17 °C and 21°–23°/18°–20 °C, day/night temperatures. Flowering was earliest with corms produced at 24°–26°/18°–20 °C and forced at 18°–20/15°–17 °C, and was significantly delayed when forced at 27°–29°/24°–26 °C. Flowering was, however, favored by 2 or 4 weeks of high temperatures (27°–29°/24°–26 °C) prior to forcing at low temperatures (18°–20°/15°–17 °C). The number of florets was not significantly affected by corm storage, forcing temperatures, or their interaction, although forcing at high temperatures tends to reduce the floret number. -
Outline of Angiosperm Phylogeny
Outline of angiosperm phylogeny: orders, families, and representative genera with emphasis on Oregon native plants Priscilla Spears December 2013 The following listing gives an introduction to the phylogenetic classification of the flowering plants that has emerged in recent decades, and which is based on nucleic acid sequences as well as morphological and developmental data. This listing emphasizes temperate families of the Northern Hemisphere and is meant as an overview with examples of Oregon native plants. It includes many exotic genera that are grown in Oregon as ornamentals plus other plants of interest worldwide. The genera that are Oregon natives are printed in a blue font. Genera that are exotics are shown in black, however genera in blue may also contain non-native species. Names separated by a slash are alternatives or else the nomenclature is in flux. When several genera have the same common name, the names are separated by commas. The order of the family names is from the linear listing of families in the APG III report. For further information, see the references on the last page. Basal Angiosperms (ANITA grade) Amborellales Amborellaceae, sole family, the earliest branch of flowering plants, a shrub native to New Caledonia – Amborella Nymphaeales Hydatellaceae – aquatics from Australasia, previously classified as a grass Cabombaceae (water shield – Brasenia, fanwort – Cabomba) Nymphaeaceae (water lilies – Nymphaea; pond lilies – Nuphar) Austrobaileyales Schisandraceae (wild sarsaparilla, star vine – Schisandra; Japanese -
Growing the Gladiolus
Volume 3 Article 1 Bulletin P85 Growing the Gladiolus 7-1-1947 Growing the Gladiolus L. C. Grove Iowa State College Follow this and additional works at: http://lib.dr.iastate.edu/bulletinp Part of the Agriculture Commons, and the Plant Sciences Commons Recommended Citation Grove, L. C. (1947) "Growing the Gladiolus," Bulletin P: Vol. 3 : Bulletin P85 , Article 1. Available at: http://lib.dr.iastate.edu/bulletinp/vol3/iss85/1 This Article is brought to you for free and open access by the Iowa Agricultural and Home Economics Experiment Station Publications at Iowa State University Digital Repository. It has been accepted for inclusion in Bulletin P by an authorized editor of Iowa State University Digital Repository. For more information, please contact [email protected]. Grove: Growing the Gladiolus g N SIO N SER V IC E, Cooperating Published by Iowa State University Digital Repository, 1947 AMES, IOWA 1 Bulletin P, Vol. 3, No. 85 [1947], Art. 1 CONTENTS Page Growth development ....................................................................,807 Propagation ................................ .. ........................................... 809 Methods ..................................................... 809 Bulbs . , .......................................................... 810 Sizes ......................................•.....................................................810 Bulb shape ............................................................. 810 Varieties .............................. 811 Flower uses ................. ...................................................................811 -
GENOME EVOLUTION in MONOCOTS a Dissertation
GENOME EVOLUTION IN MONOCOTS A Dissertation Presented to The Faculty of the Graduate School At the University of Missouri In Partial Fulfillment Of the Requirements for the Degree Doctor of Philosophy By Kate L. Hertweck Dr. J. Chris Pires, Dissertation Advisor JULY 2011 The undersigned, appointed by the dean of the Graduate School, have examined the dissertation entitled GENOME EVOLUTION IN MONOCOTS Presented by Kate L. Hertweck A candidate for the degree of Doctor of Philosophy And hereby certify that, in their opinion, it is worthy of acceptance. Dr. J. Chris Pires Dr. Lori Eggert Dr. Candace Galen Dr. Rose‐Marie Muzika ACKNOWLEDGEMENTS I am indebted to many people for their assistance during the course of my graduate education. I would not have derived such a keen understanding of the learning process without the tutelage of Dr. Sandi Abell. Members of the Pires lab provided prolific support in improving lab techniques, computational analysis, greenhouse maintenance, and writing support. Team Monocot, including Dr. Mike Kinney, Dr. Roxi Steele, and Erica Wheeler were particularly helpful, but other lab members working on Brassicaceae (Dr. Zhiyong Xiong, Dr. Maqsood Rehman, Pat Edger, Tatiana Arias, Dustin Mayfield) all provided vital support as well. I am also grateful for the support of a high school student, Cady Anderson, and an undergraduate, Tori Docktor, for their assistance in laboratory procedures. Many people, scientist and otherwise, helped with field collections: Dr. Travis Columbus, Hester Bell, Doug and Judy McGoon, Julie Ketner, Katy Klymus, and William Alexander. Many thanks to Barb Sonderman for taking care of my greenhouse collection of many odd plants brought back from the field. -
Managing Watsonia Invasion in the Threatened Plant Communities of South-West Australia’S Clay-Based Wetlands
Managing Watsonia invasion in the threatened plant communities of south-west Australia’s clay-based wetlands. K. Brown, G. Paczkowska, B. Huston and N. Withnell. Department of Environment and Conservation, W.A. Email: [email protected] The Seasonal Clay-based Wetlands of South-west Australia While the majority of seasonal wetlands in south-west Australia are connected to the regional ground water, there are a series of wetlands found on clay substrates that rely solely on rainwater to fill. These wetlands are characterised by temporally overlapping suites of annual herbs that flower and set seed as the wetlands dry through spring. Over summer the clay substrates dry to impervious pans. The plant communities of clay-based wetlands comprise a flora of over 600. At least 50% are annual or perennial herbs, 16 occur only on the clay-pans and many are rare or restricted (Figure 1). The seasonally inundated clays that support these communities are relatively productive agricultural soils and many were cleared soon after settlement. Those that remained intact were largely located on the Swan Coastal Plain in close proximity to metropolitan Perth. In more recent years large areas have disappeared under urban development and today the plant communities of seasonal clay-based wetlands are amongst the most threatened in Western Australia. The small and fragmented nature of these remaining wetlands leaves them vulnerable to a range of threatening processes. In particular weed invasion, specifically by the South African geophyte Watsonia (Watsonia meriana var. bulbillifera), is a major threat. Watsonia can disperse via cormels (tiny corms that develop along the flowering stem at the end of the flowering season), into relatively undisturbed bushland remnants, forming dense stands that effectively displace the diverse herbaceous understorey (Figure 2). -
Watsonia Workshop Proceedings of a Workshop Held at the Department of Conservation and Land Management (CALM) on August 4 1993
Plant Protection Quarterly Vol.8(3) 1993 77 Watsonia Workshop Proceedings of a workshop held at the Department of Conservation and Land Management (CALM) on August 4 1993. Organized by CALMs Science and Information Division and funded by the WA Roadside Conservation Committee. Editors: J. Patrick Pigott, WA Herbarium, Science and Information Division, Department of Conservation and Land Management, PO Box 104, Como, WA 6152, Australia. C. Mary Gray, Environmental Scientist, 24 Hillview Road, Mt Lawley, WA 6050, Australia. Western Australian species of Watsonia Neville Marchant, Acting Director, WA Herbarium, Science and Information Division, Department of Conservation and Land Management, PO Box 104, Como, WA 6152, Australia. Introduction How and when did watsonias come with settlers who arrived in Western Aus- Watsonia in Western Australia is an unu- to WA? tralia well after Georgiana Molloy. sual weed group in that there are about The characteristic of Watsonia which There are 52 species of Watsonia recog- eight species of the one genus in the State. brought so many species to this State is nized in a comprehensive treatment pub- A whole suite of species and their vari- that they have very attractive flowers. In lished in 1989 by Peter Goldblatt who has ants were introduced as garden plants in January 1830, en route to Fremantle, when reviewed all of the species described since the early days of the Swan River Colony. travellers to Western Australia called into the first one was published in 1754. The In their native habitats in southern Af- Cape Town, Georgiana Molloy spent £7 type of study made by Goldblatt, system- rica there are about 52 species of Watsonia, 17s 6d on seeds from the Cape, among atic research, entails the detailed exami- 34 of them occurring in the Cape area them oleanders, Cape gooseberries and a nation of herbarium material and litera- which has a similar climate to that of pink lily, the Watsonia. -
Insights from Microsporogenesis in Asparagales
EVOLUTION & DEVELOPMENT 9:5, 460–471 (2007) Constraints and selection: insights from microsporogenesis in Asparagales Laurent Penet,a,1,Ã Michel Laurin,b Pierre-Henri Gouyon,a,c and Sophie Nadota aLaboratoire Ecologie, Syste´matique et Evolution, Batiment 360, Universite´ Paris-Sud, 91405 Orsay Ce´dex, France bUMR CNRS 7179, Universite´ Paris 6FPierre & Marie Curie, 2 place Jussieu, Case 7077, 75005 Paris, France cMuse´um National d’Histoire Naturelle, De´partement de Syste´matique et Evolution Botanique, 12 rue Buffon, 75005 Paris CP 39, France ÃAuthor for correspondence (email: [email protected]) 1Current address: Department of Biological Sciences, University of Pittsburgh, 4249 Fifth & Ruskin, Pittsburgh, PA 15260, USA. SUMMARY Developmental constraints have been proposed different characteristics of microsporogenesis, only cell to interfere with natural selection in limiting the available wall formation appeared as constrained. We show that set of potential adaptations. Whereas this concept has constraints may also result from biases in the correlated long been debated on theoretical grounds, it has been occurrence of developmental steps (e.g., lack of successive investigated empirically only in a few studies. In this article, cytokinesis when wall formation is centripetal). We document we evaluate the importance of developmental constraints such biases and their potential outcomes, notably the during microsporogenesis (male meiosis in plants), with an establishment of intermediate stages, which allow emphasis on phylogenetic patterns in Asparagales. Different development to bypass such constraints. These insights are developmental constraints were tested by character discussed with regard to potential selection on pollen reshuffling or by simulated distributions. Among the morphology. INTRODUCTION 1991) also hindered tests using the concept (Pigliucci and Kaplan 2000). -
The Effect of Slashing on the Growth of Watsonia Meriana (L.) Mill. Cv Bulbillifera in the Adelaide Hills
Plant Protection Quarterly Vol.8(3) 1993 85 ment of Conservation and Land Manage- ment and Mr. B. Lord of the Charles Sturt University, is gratefully acknowledged. The effect of slashing on the growth of Watsonia meriana (L.) Mill. cv bulbillifera in the Adelaide Hills References Australian Institute of Environmental Studies (1976). ‘The Threat of Weeds to P.A. Wilson and J.G. Conran, Department of Botany, University of Ad- Bushland, a Victorian Study’. (Inkata elaide, SA 5006, Australia. Press, Melbourne, Australia). Gillison, A.N. (1984). Gradient oriented sampling for resource surveys. In ‘Sur- Summary vey Methods for Nature Conservation’, In order to control Watsonia meriana cv suggested that it is merely a local sport ed. K. Myers and D.R. Margules. Vol 2. bulbillifera by slashing, it is necessary to which has been introduced into cultiva- Proceedings of Workshop 1983. prevent flowering and bulbil produc- tion. Currently Watsonia meriana cv Heddle, E.M. (1980). Effects of Changes in tion, as well as reduce the strength of the bulbillifera is considered a weed in Aus- Soil Moisture on the Nature Vegetation corm. The effects of slashing at a tralia, Mauritius, Réunion (Goldblatt of the Northern Swan Coastal Plain, number of heights, and at a range of 1989) and New Zealand (Parsons and Western Australia. Bulletin 92, Forests times throughout the plant’s life-history Cuthbertson 1992). The earliest record in Department of Western Australia. were investigated both for mature South Australia dates from 1842 at Lamont, D. A. (1987). Vegetation Survey plants and those derived from bulbils. Camden Park, Adelaide (Parsons and of Serpentine National Park, Map Plants derived from bulbils require Cuthbertson 1992). -
Mullins Hankins 2906-1331
ADDING CUT FLOWERS MAY INCREASE PROFITS Andy Hankins, Extension Specialist-Alternative Agriculture - Virginia State University Reviewed by Chris Mullins, Virginia State University 2018 Vegetable growers who sell produce at farmers' markets, at roadside stands, to restaurants and to local supermarkets may find that they can bring in additional income by adding fresh cut flowers to the inventory of products they sell. A number of benefits can be gained from adding cut flowers to a vegetable marketing operation. Cut flowers add diversity. Customers at roadside stands and at farmers markets like to have many choices. The brilliant colors of a 1/4-acre plot of cut flowers growing beside a roadside stand certainly add visual appeal to potential customers coming down the highway. Restaurant managers need fresh cut flowers for table arrangements. They may be just as interested in buying flowers as they are in buying vegetables. All supermarkets now offer sleeved bunches of fresh cut flowers in glass front coolers in their produce sections. Those store managers need flower growers who can deliver sleeved bunches ready for sale. Many growers who interplant rows of cut flowers among rows of vegetables have noticed a reduction in damage to their vegetable crops by pest insects. The flower crops often harbor populations of beneficial predatory and parasitic insects that control the pest species. Production of cut flowers requires many of the same resources as production of vegetables such as irrigation, transplanting equipment, cultivators, etc. The greatest conflict between these two enterprises occurs in the walk-in cooler. Vegetables like broccoli give off ethylene gas, which can cause severe damage to blooming flowers. -
Wild Watsonia (DPI Vic)
May 2000 Wild watsonia LC0251 Keith Turnbull Research Institute, Frankston ISSN 1329-833X This Landcare Note describes the weed Wild watsonia, West Gippsland, the central highlands and the Geelong Watsonia meriana var. bulbillifera, and related species region. and outlines options for its management. Description Common Name An erect perennial herb forming large clumps; similar to Wild watsonia, bulbil watsonia gladiolus, with strap-like leaves, slender reddish flowering stems 0.5 to 2 m high, pink, orange or red flowers, Botanical Name underground corms and clusters of small corms (known as Watsonia meriana (L.) Miller var. bulbillifera (J.W. bulbils or cormils) on the stems. Leaves and flowering Matthews & L. Bolus) D.A. Cooke heads are produced annually. Family Iridaceae (Iris family) Status Under the Catchment and Land Protection Act, wild watsonia is a Regionally Controlled Weed in the Glenelg, Corangamite, Port Phillip West, Port Phillip East, North East, East Gippsland and West Gippsland Regions. Land owners in areas where wild watsonia is Regionally Controlled must take all reasonable steps to control it and prevent its spread on their land and the roadsides which adjoin their land. Wild watsonia is mainly a weed of roadsides, railway reserves, the edges of water courses, open woodland, unimproved pastures and neglected areas. Origin and Distribution Native to South Africa, wild watsonia was originally introduced to Australia as a garden ornamental. It was considered naturalised in Victoria by 1907 and was spread widely in the 1940s as a fashionable garden plant. It is also a weed in New Zealand and on the Indian Ocean islands of Mauritius and Reunion.