Agapanthus Praecox Subsp. Orientalis African Lily, Blue Lily, Lily of the Nile

Total Page:16

File Type:pdf, Size:1020Kb

Agapanthus Praecox Subsp. Orientalis African Lily, Blue Lily, Lily of the Nile Agapanthus praecox subsp. orientalis African Lily, Blue Lily, Lily of the Nile There is some controversy about the number of species of Agapanthus, depending on the source this can vary from six to ten. And in spite of the various common names (African Lily, Lily of the Nile, Blue Lily), Agapanthus isn’t a lily at all, that is, not in the family Liliaceae, nor does it come from anywhere near the Nile. In fact, all Agapanthus species come from South Africa, between the Limpopo River (‘all set about with Fever Trees’) and the Cape of Good Hope. Agapanthus praecox subsp. orientalis, the most commonly grown species, comes from the Eastern Cape and southern KwaZulu-Natal1. Amaryllidaceae – Liliaceae Ovary sits below the petals Ovary sits above the petals The genus Agapanthus has been placed in the Amaryllidaceae family which includes Daffodils, Nerines and Naked Ladies, although some consider it may sit better in its own family, the Agapanthaceae, or even with garlic and onions in the Alliaceae2. Flowers of Amaryllidaceae typically have the petals attached above the ovary; those of lilies (Liliaceae) have the petals attached below the ovary. In Sydney the blue and white flowers of Agapanthus signal the approach of summer and Christmas festivities. Agapanthus flowers are loved by some, loathed by others. In recent years, Agapanthus has yet again become a fashionable garden plant. Agapanthus sets seed readily and is an invasive weed in the Blue Mountains, on Lord Howe Island and in parts of Victoria and Western Australia. If you live near bushland and grow Agapanthus in your garden, local councils and bushland regenerators will be appreciative if you remove old flower heads before they have a chance to set seed. 1Alice Notten, Kirstenbosch National Botanic Gardens, 2004. South African National Biodiversity Institute, South Africa. http://www.plantzafrica.com/plantab/agapanpraecox.htm 2Wikipedia: http://en.wikipedia.org/wiki/Agapanthus Map showing distribution in South Africa modified from Red List of South African Plants: http://redlist.sanbi.org/species.php?species=481-18 Alison Downing, Kevin Downing & Brian Atwell, 9.12.2013 Department of Biological Sciences Beware of the Agapanthus! Do Not Run! .
Recommended publications
  • Summer Bulbs
    Garden Mastery Tips June 2008 from Clark County Master Gardeners Summer Bulbs Wasn't it easy to get that wonderful spring color? You dug a hole last fall and dropped in crocus, daffodil, hyacinth or tulip bulbs. Covered them up and went back inside to wait until spring. The hardest part was probably choosing which bulbs and colors to plant. Wouldn't it be nice to take care of your summer garden color the same way? Well, you can. There are summer bulbs, corms and rhizomes that need the same amount of care. You dig a hole, drop them in and voila!, in a few weeks, you have summer color. Again, the hardest part will be choosing what to plant. Here are some suggestions for you. Agapanthus – Agreeable Agapanthus, Love Flower Amaryllis Belladonna – What Do You Say to a Naked Lady? (Amaryllis belladonna) Calla Lilies – Supercalifragilisticexpialidocious "Lilies" Canna flowers are similar to Gladiolus, large clusters of flowers. But think steroids. These plants are big, brash and bold. Canna rhizomes should be planted in loose, fertile, well-drained soil. They don't have a top or bottom so just lay them in the ground and cover with about two inches of soil after all danger of hard frost has passed. For a really showy statement in your garden, plant a group. Again, the lazy gardener can mulch over the cannas and take a chance on their coming up the next year. A website full of information on Cannas can be found at Horn Canna Farm’s site. Croscosmia – Crocosmia Dahlias – Dahlia Success Eucomis – Eucomis Gladiolus is native to sub-Saharan Africa and contains about 260 species.
    [Show full text]
  • Success with Herbaceous Perennials
    Landscape Basics: Success with Herbaceous Perennials Bodie Pennisi, Paul Thomas and Sheri Dorn Department of Horticulture hether in a commercial installation or residen- fewer pest problems, require less water and pruning, Wtial garden, perennial plants can be successfully and have an extended flowering time. This information used to offer more landscaping choices, distinguish can be acquired from books, annual trade confer- your firm from the competition and create a niche for ences and Extension publications (refer to “Additional your landscape business. Perennial plants are complex, Resources” at the end of this publication). An excellent and it is best to contract or hire a professional land- way to see how new selections perform is to visit the scape architect for the design phase and train knowl- University of Georgia Trial Gardens located on campus edgeable staff in proper maintenance later on. in Athens (http://ugatrial.hort.uga.edu/). With a rich history of plant introductions, hybridiza- This publication is intended to provide the basics of tion and selection, we can now enjoy plants in Georgia perennial plant biology, ideas on design and installa- that until recently were once found only on a remote tion, and information on cultivation and maintenance mountain slope in Asia or a tropical rainforest in South of perennial beds. It should also serve as a quick guide America. The perennial plant trade offers more than for the most common and recommended perennials 3,600 species and cultivated varieties, and more are for Georgia. Common-sense tips from a professional added each year. With such an extensive palette, how landscaper’s perspective are also included.
    [Show full text]
  • 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
    [Show full text]
  • The Fairchild Tropical Garden NIXON SMILEY ______1
    ~GAZ.NE AMERICAN HORTI CULTURAL SOCIETY A vnion of the Ame'rican Horticultuml Society and the American Ho·rticultural Council 1600 BLADENSB URG ROAD, NORTHEAST . WASHINGTON 2, D. C. For Un ited H mticulture *** to accumulate, increase, and disseminate horticultuml infmmation B. Y. MORRISON, Editor Di?-ec to?'S T enns Expiring 1960 J AMES R. H ARLOW, Managing Editor D ONOVAN S. CORRELL T exas CARL "V. F ENN I NGER Editorial Committee Pennsylvania W. H . HODGE W'. H . HODGE, Chainnan Pen nS)1 Ivan i(~ ] OHN L. CREECH A. J. IRVI NG Yo?'k FREDElRI C P. L EE New "VILLIAM C. STEERE CONRAD B. LI NK New York CURTIS MAY FREDERICK G. MEYER T erms Ex1Jil'ing 1961 STUART M. ARMSTRONG 'WILBUR H. YOUNGMAN Maryland J OHN L. CREECH Maryland Officers 'WILLIAM H . FREDERICK, JR. DelawQ.j·e PR ES IDENT FRANCIS PATTESON-KNIGHT RICHARD P . 'WHITE V il'ginia Washington, D. C. DONALD WYMAN 111 assachv.setts FIRST VICE·PRESIDENT Tenns Expiring 1962 DONALD W YMAN Jamaica Plain, Massachusetts FREDERIC P. LEE Maryland HENRY T. SKINNER SECOND VICE- PRESIDENT Distl'ict of Columba STUART M. ARMSTRONG CEORGE H. SPALDING Silvel' Spring, Mal'yland California RICHARD P. WHITE SECRETARY-TREASURER District of Columbia OLIVE E. WEATHERELL AN NE " VERTSNER WOOD Washington, D. C. Pennsylvania The Amel'ican Ho'yticvltw'al Magazine is the official publication of the American Horticultural Society and is issued fo ur times a year during the q uarters commencing with January, April , July and October. It is devoted to the dissemination of knowledge in the science and art of growing ornamental plants, fruits, vegetables, and related subjects.
    [Show full text]
  • Complete Chloroplast Genomes Shed Light on Phylogenetic
    www.nature.com/scientificreports OPEN Complete chloroplast genomes shed light on phylogenetic relationships, divergence time, and biogeography of Allioideae (Amaryllidaceae) Ju Namgung1,4, Hoang Dang Khoa Do1,2,4, Changkyun Kim1, Hyeok Jae Choi3 & Joo‑Hwan Kim1* Allioideae includes economically important bulb crops such as garlic, onion, leeks, and some ornamental plants in Amaryllidaceae. Here, we reported the complete chloroplast genome (cpDNA) sequences of 17 species of Allioideae, fve of Amaryllidoideae, and one of Agapanthoideae. These cpDNA sequences represent 80 protein‑coding, 30 tRNA, and four rRNA genes, and range from 151,808 to 159,998 bp in length. Loss and pseudogenization of multiple genes (i.e., rps2, infA, and rpl22) appear to have occurred multiple times during the evolution of Alloideae. Additionally, eight mutation hotspots, including rps15-ycf1, rps16-trnQ-UUG, petG-trnW-CCA , psbA upstream, rpl32- trnL-UAG , ycf1, rpl22, matK, and ndhF, were identifed in the studied Allium species. Additionally, we present the frst phylogenomic analysis among the four tribes of Allioideae based on 74 cpDNA coding regions of 21 species of Allioideae, fve species of Amaryllidoideae, one species of Agapanthoideae, and fve species representing selected members of Asparagales. Our molecular phylogenomic results strongly support the monophyly of Allioideae, which is sister to Amaryllioideae. Within Allioideae, Tulbaghieae was sister to Gilliesieae‑Leucocoryneae whereas Allieae was sister to the clade of Tulbaghieae‑ Gilliesieae‑Leucocoryneae. Molecular dating analyses revealed the crown age of Allioideae in the Eocene (40.1 mya) followed by diferentiation of Allieae in the early Miocene (21.3 mya). The split of Gilliesieae from Leucocoryneae was estimated at 16.5 mya.
    [Show full text]
  • 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.
    [Show full text]
  • Atoll Research Bulletin No. 503 the Vascular Plants Of
    ATOLL RESEARCH BULLETIN NO. 503 THE VASCULAR PLANTS OF MAJURO ATOLL, REPUBLIC OF THE MARSHALL ISLANDS BY NANCY VANDER VELDE ISSUED BY NATIONAL MUSEUM OF NATURAL HISTORY SMITHSONIAN INSTITUTION WASHINGTON, D.C., U.S.A. AUGUST 2003 Uliga Figure 1. Majuro Atoll THE VASCULAR PLANTS OF MAJURO ATOLL, REPUBLIC OF THE MARSHALL ISLANDS ABSTRACT Majuro Atoll has been a center of activity for the Marshall Islands since 1944 and is now the major population center and port of entry for the country. Previous to the accompanying study, no thorough documentation has been made of the vascular plants of Majuro Atoll. There were only reports that were either part of much larger discussions on the entire Micronesian region or the Marshall Islands as a whole, and were of a very limited scope. Previous reports by Fosberg, Sachet & Oliver (1979, 1982, 1987) presented only 115 vascular plants on Majuro Atoll. In this study, 563 vascular plants have been recorded on Majuro. INTRODUCTION The accompanying report presents a complete flora of Majuro Atoll, which has never been done before. It includes a listing of all species, notation as to origin (i.e. indigenous, aboriginal introduction, recent introduction), as well as the original range of each. The major synonyms are also listed. For almost all, English common names are presented. Marshallese names are given, where these were found, and spelled according to the current spelling system, aside from limitations in diacritic markings. A brief notation of location is given for many of the species. The entire list of 563 plants is provided to give the people a means of gaining a better understanding of the nature of the plants of Majuro Atoll.
    [Show full text]
  • Rapid in Vitro Micropropagation of Agapanthus Praecox
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector South African Journal of Botany 86 (2013) 46–50 Contents lists available at SciVerse ScienceDirect South African Journal of Botany journal homepage: www.elsevier.com/locate/sajb Rapid in vitro micropropagation of Agapanthus praecox Ponnusamy Baskaran, Johannes Van Staden ⁎ Research Centre for Plant Growth and Development, School of Life Sciences, University of KwaZulu-Natal Pietermaritzburg, Scottsville 3209, South Africa article info abstract Article history: In vitro micropropagation and acclimatization for the ornamental Agapanthus praecox, are reported. The influ- Received 6 March 2012 ence of different growth regulators on shoot multiplication from shoot-tip explants of A. praecox was inves- Received in revised form 19 November 2012 tigated. Prolific shoot multiplication (47.3±1.96 shoots per explant) was achieved on Murashige and Skoog Accepted 28 January 2013 (MS) medium supplemented with 22.2 μM benzyladenine (BA), 2.9 μM indole-3-acetic acid (IAA), and Available online 6 March 2013 4.5 μM thidiazuron (TDZ). Shoots were rooted on half-strength MS basal medium supplemented with μ μ Edited by NJ Taylor 5.7 M IAA and 2.5 M 2-isopentenyladenine (2iP) with 11.3±0.78 roots per shoot. The in vitro-raised plants were established successfully in a 1:1 (v/v) vermiculite:sand mixture when maintained in a greenhouse with Keywords: 100% survival. The elongated shoots (more than 5 cm in length) were treated for rooting and acclimatization Agapanthus praecox in a moistened (5.7 μM IAA and 2.5 μM 2iP) vermiculite:sand (1:1 v/v) mixture, first in the misthouse and In vitro regeneration then in the greenhouse.
    [Show full text]
  • Algorithms of Embryo Morphogenesis in Agapanthus Praecox Willd. (Alliaceae) in Monocotyly, Dicotyly and Transitional Forms
    ACTA BIOLOGICA CRACOVIENSIA Series Botanica 45/1: 161–165, 2003 ALGORITHMS OF EMBRYO MORPHOGENESIS IN AGAPANTHUS PRAECOX WILLD. (ALLIACEAE) IN MONOCOTYLY, DICOTYLY AND TRANSITIONAL FORMS GALINA E. TITOVA* Department of Embryology and Reproductive Biology, Komarov Botanical Institute, Prof. Popov Str. 2, 197376 St. Petersburg, Russia Received October 9, 2002; revision accepted February 21, 2003 The study found that the monocot Agapanthus praecox from different cultivation localities has a stable tendency to develop dicotyledonous together with monocotyledonous and transitional forms, with various degrees of cotyledonary fusion. The morphogenetic events during embryogenesis leading to this diversity are presented and analyzed. Key words: Agapanthus praecox, Alliaceae, embryogenesis, monocotyly. INTRODUCTION MATERIALS AND METHODS The ability of monocot plants to form dicotyledon- Mature seeds of A. praecox were collected from the ous embryos is a question of great theoretical Royal Botanical Gardens of Sydney, Australia significance in connection with the problem of the (1998) and the greenhouses of the Komarov Botani- origin of monocotyly. Earlier authors gave data on cal Institute, St. Petersburg, Russia (2000, 2001); the spontaneous formation of typical dicotyledon- material for study of embryogenesis was fixed at the ous embryos in some Alliaceae (Agapanthus umbel- Komarov Botanical Institute. Seed germination was latus – Coulter and Land, 1914), Amaryllidaceae monitored under laboratory conditions (18–20˚C, (Cyrthanthus sanguineus – Farrell, 1914) and natural illumination) in no less than 500 seeds from Araceae (Colocasia antiquorum – Suessenguth, each locality of cultivation. For study of embryogen- 1921). For a long time these data have been criticized esis, flowers were artificially pollinated and the em- but never reinvestigated. A single work on the em- bryos were fixed.
    [Show full text]
  • Lesson 3 RECOGNISING PLANT FAMILIES and IDENTIFYING PLANTS Aim Distinguish Between Different Plant Families and to Become Profi
    Lesson 3 RECOGNISING PLANT FAMILIES AND IDENTIFYING PLANTS Aim Distinguish between different plant families and to become proficient at identifying plants. The best way to build your ability to identify plants is by working with or handling a variety of different plants on a daily basis. The first ten plant names you learn are always much more difficult than the next ninety. Similarly, the first 100 names are always much more difficult than the next 900. If you plan to be a skilled gardener, landscape designer, or horticulturist: you need to learn to identify hundreds of different plants. As you have seen earlier; there is a system in identifying plant names. BECOME FAMILIAR WITH PLANT FAMILIES If you can get to know the way the system works, and the broad categories, the whole thing starts to make a great deal more sense. Each new name you confront is able to be associated with things and remembered more easily. FOR EXAMPLE: “When I see a plant with a daisy flower, I immediately know that it is in the Asteraceae family. Even if the genus is new to me, I will be more likely to remember it because I’m not only thinking: This is the genus of this new plant , but I am also thinking: This new genus is in the Asteraceae family. In essence, my brain is registering two pieces of information instead of one and that doubles the likelihood of me remembering the plant. BECOME FAMILIAR WITH LATIN Plant naming is based on the ancient Roman language of Latin.
    [Show full text]
  • Assembling the Tree of the Monocotyledons: Plastome Sequence Phylogeny and Evolution of Poales Author(S) :Thomas J
    Assembling the Tree of the Monocotyledons: Plastome Sequence Phylogeny and Evolution of Poales Author(s) :Thomas J. Givnish, Mercedes Ames, Joel R. McNeal, Michael R. McKain, P. Roxanne Steele, Claude W. dePamphilis, Sean W. Graham, J. Chris Pires, Dennis W. Stevenson, Wendy B. Zomlefer, Barbara G. Briggs, Melvin R. Duvall, Michael J. Moore, J. Michael Heaney, Douglas E. Soltis, Pamela S. Soltis, Kevin Thiele, and James H. Leebens-Mack Source: Annals of the Missouri Botanical Garden, 97(4):584-616. 2010. Published By: Missouri Botanical Garden DOI: URL: http://www.bioone.org/doi/full/10.3417/2010023 BioOne (www.bioone.org) is a a nonprofit, online aggregation of core research in the biological, ecological, and environmental sciences. BioOne provides a sustainable online platform for over 170 journals and books published by nonprofit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Web site, and all posted and associated content indicates your acceptance of BioOne’s Terms of Use, available at www.bioone.org/ page/terms_of_use. Usage of BioOne content is strictly limited to personal, educational, and non- commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research. ASSEMBLING THE TREE OF THE Thomas J. Givnish,2 Mercedes Ames,2 Joel R. MONOCOTYLEDONS: PLASTOME McNeal,3 Michael R. McKain,3 P. Roxanne Steele,4 Claude W. dePamphilis,5 Sean W.
    [Show full text]
  • FULL ACCOUNT FOR: Agapanthus Praecox Global Invasive Species Database (GISD) 2021. Species Profile Agapanthus Praecox. Available
    FULL ACCOUNT FOR: Agapanthus praecox Agapanthus praecox System: Terrestrial Kingdom Phylum Class Order Family Plantae Magnoliophyta Liliopsida Liliales Liliaceae Common name African-lily (English), lirio africano (Spanish, Argentina), agapanthus (English), bloulelie (Afrikaans), lily-of-the-Nile (English), agapanto (Spanish, Argentina), common agapanthus (English), flor de Navidad (Spanish, Argentina), blue lily (English) Synonym Tulbaghia praecox , (Willd.) Kuntze Similar species Agapanthus africanus, Arthropodium cirratum Summary Agapanthus praecox is a rhizomatous herb that is native to South Africa, along with its subspecies, A. praecox subsp. minimus, A. praecox subsp. orientalis and A. praecox subsp. praecox. Most cultivated agapanthus are cultivars or hybrids of A. praecox, and the subspecies readily hybridise. Agapanthus has characteristic composite florescences that are white or blue and tubular and is commonly planted as an ornamental. view this species on IUCN Red List Species Description Agapanthus praecox is a rhizomatous, perennial herb. Its leaves are robust, strap-like and evergreen and there are 6 - 20 leaves per individual plant. The leaves grow in dense clumps from bulb up to 60 cm high. The composite inflorescences are large and round, made up of tubular flowers. These are either coloured white or light blue. Inflorescences can grow up to 1.2 m in summer. (ARC 2009; FloraBase 2010; Notten 2004; Weeds of Blue Mountains Bushland 2010). \n Notes Known subspecies of Agapanthus praecox include A. praecox ssp. minimus, A. praecox ssp. orientalis and A. praecox ssp. praecox. Subspecies readily hybridise, especially when grown in close proximity. In the Auckland region of New Zealand, the sale, propogation, planting and distribution of A. praecox is prohibited.
    [Show full text]