Hymenocallis Littoralis
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Boophone Disticha
Micropropagation and pharmacological evaluation of Boophone disticha Lee Cheesman Submitted in fulfilment of the academic requirements for the degree of Doctor of Philosophy Research Centre for Plant Growth and Development School of Life Sciences University of KwaZulu-Natal, Pietermaritzburg April 2013 COLLEGE OF AGRICULTURE, ENGINEERING AND SCIENCES DECLARATION 1 – PLAGIARISM I, LEE CHEESMAN Student Number: 203502173 declare that: 1. The research contained in this thesis, except where otherwise indicated, is my original research. 2. This thesis has not been submitted for any degree or examination at any other University. 3. This thesis does not contain other persons’ data, pictures, graphs or other information, unless specifically acknowledged as being sourced from other persons. 4. This thesis does not contain other persons’ writing, unless specifically acknowledged as being sourced from other researchers. Where other written sources have been quoted, then: a. Their words have been re-written but the general information attributed to them has been referenced. b. Where their exact words have been used, then their writing has been placed in italics and inside quotation marks, and referenced. 5. This thesis does not contain text, graphics or tables copied and pasted from the internet, unless specifically acknowledged, and the source being detailed in the thesis and in the reference section. Signed at………………………………....on the.....….. day of ……......……….2013 ______________________________ SIGNATURE i STUDENT DECLARATION Micropropagation and pharmacological evaluation of Boophone disticha I, LEE CHEESMAN Student Number: 203502173 declare that: 1. The research reported in this dissertation, except where otherwise indicated is the result of my own endeavours in the Research Centre for Plant Growth and Development, School of Life Sciences, University of KwaZulu-Natal, Pietermaritzburg. -
Guide to the Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- LILIACEAE
Guide to the Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- LILIACEAE LILIACEAE de Jussieu 1789 (Lily Family) (also see AGAVACEAE, ALLIACEAE, ALSTROEMERIACEAE, AMARYLLIDACEAE, ASPARAGACEAE, COLCHICACEAE, HEMEROCALLIDACEAE, HOSTACEAE, HYACINTHACEAE, HYPOXIDACEAE, MELANTHIACEAE, NARTHECIACEAE, RUSCACEAE, SMILACACEAE, THEMIDACEAE, TOFIELDIACEAE) As here interpreted narrowly, the Liliaceae constitutes about 11 genera and 550 species, of the Northern Hemisphere. There has been much recent investigation and re-interpretation of evidence regarding the upper-level taxonomy of the Liliales, with strong suggestions that the broad Liliaceae recognized by Cronquist (1981) is artificial and polyphyletic. Cronquist (1993) himself concurs, at least to a degree: "we still await a comprehensive reorganization of the lilies into several families more comparable to other recognized families of angiosperms." Dahlgren & Clifford (1982) and Dahlgren, Clifford, & Yeo (1985) synthesized an early phase in the modern revolution of monocot taxonomy. Since then, additional research, especially molecular (Duvall et al. 1993, Chase et al. 1993, Bogler & Simpson 1995, and many others), has strongly validated the general lines (and many details) of Dahlgren's arrangement. The most recent synthesis (Kubitzki 1998a) is followed as the basis for familial and generic taxonomy of the lilies and their relatives (see summary below). References: Angiosperm Phylogeny Group (1998, 2003); Tamura in Kubitzki (1998a). Our “liliaceous” genera (members of orders placed in the Lilianae) are therefore divided as shown below, largely following Kubitzki (1998a) and some more recent molecular analyses. ALISMATALES TOFIELDIACEAE: Pleea, Tofieldia. LILIALES ALSTROEMERIACEAE: Alstroemeria COLCHICACEAE: Colchicum, Uvularia. LILIACEAE: Clintonia, Erythronium, Lilium, Medeola, Prosartes, Streptopus, Tricyrtis, Tulipa. MELANTHIACEAE: Amianthium, Anticlea, Chamaelirium, Helonias, Melanthium, Schoenocaulon, Stenanthium, Veratrum, Toxicoscordion, Trillium, Xerophyllum, Zigadenus. -
– the 2020 Horticulture Guide –
– THE 2020 HORTICULTURE GUIDE – THE 2020 BULB & PLANT MART IS BEING HELD ONLINE ONLY AT WWW.GCHOUSTON.ORG THE DEADLINE FOR ORDERING YOUR FAVORITE BULBS AND SELECTED PLANTS IS OCTOBER 5, 2020 PICK UP YOUR ORDER OCTOBER 16-17 AT SILVER STREET STUDIOS AT SAWYER YARDS, 2000 EDWARDS STREET FRIDAY, OCTOBER 16, 2020 SATURDAY, OCTOBER 17, 2020 9:00am - 5:00pm 9:00am - 2:00pm The 2020 Horticulture Guide was generously underwritten by DEAR FELLOW GARDENERS, I am excited to welcome you to The Garden Club of Houston’s 78th Annual Bulb and Plant Mart. Although this year has thrown many obstacles our way, we feel that the “show must go on.” In response to the COVID-19 situation, this year will look a little different. For the safety of our members and our customers, this year will be an online pre-order only sale. Our mission stays the same: to support our community’s green spaces, and to educate our community in the areas of gardening, horticulture, conservation, and related topics. GCH members serve as volunteers, and our profits from the Bulb Mart are given back to WELCOME the community in support of our mission. In the last fifteen years, we have given back over $3.5 million in grants to the community! The Garden Club of Houston’s first Plant Sale was held in 1942, on the steps of The Museum of Fine Arts, Houston, with plants dug from members’ gardens. Plants propagated from our own members’ yards will be available again this year as well as plants and bulbs sourced from near and far that are unique, interesting, and well suited for area gardens. -
Scaevola Taccada (Gaertn.) Roxb
BioInvasions Records (2021) Volume 10, Issue 2: 425–435 CORRECTED PROOF Rapid Communication First record of naturalization of Scaevola taccada (Gaertn.) Roxb. (Goodeniaceae) in southeastern Mexico Gonzalo Castillo-Campos1,*, José G. García-Franco2 and M. Luisa Martínez2 1Red de Biodiversidad y Sistemática, Instituto de Ecología, A.C., Xalapa, Veracruz, 91073, México 2Red de Ecología Funcional, Instituto de Ecología, A.C. Xalapa, Veracruz, 91073, México Author e-mails: [email protected] (GCC), [email protected] (JGGF), [email protected] (MLM) *Corresponding author Citation: Castillo-Campos G, García- Franco JG, Martínez ML (2021) First Abstract record of naturalization of Scaevola taccada (Gaertn.) Roxb. (Goodeniaceae) Scaevola taccada (Gaertn.) Roxb. is native of Asia and eastern Africa but has been in southeastern Mexico. BioInvasions introduced into the Americas as an ornamental urban plant. This paper reports, for Records 10(2): 425–435, https://doi.org/10. the first time, the presence of Scaevola taccada in natural environments from 3391/bir.2021.10.2.21 southeastern Mexico. Several populations of S. taccada were identified during a Received: 23 July 2020 botanical survey of the coastal dunes of the Cozumel Island Biosphere Reserve Accepted: 22 October 2020 (State of Quintana Roo, Mexico) aimed at recording the most common plant Published: 22 January 2021 species. Scaevola taccada is considered as an invasive species of coastal areas in this region. Evidence of its invasiveness is suggested by the fact that populations Handling editor: Oliver Pescott consisting of individuals of different size classes are found distributed throughout Thematic editor: Stelios Katsanevakis the island. Furthermore, they appear to belong to different generations since we Copyright: © Castillo-Campos et al. -
Phyllosticta Hymenocallidicola Fungal Planet Description Sheets 139
138 Persoonia – Volume 27, 2011 Phyllosticta hymenocallidicola Fungal Planet description sheets 139 Fungal Planet 95 – 6 December 2011 Phyllosticta hymenocallidicola Crous, Summerell & Romberg, sp. nov. Phyllostictae citricarpae similis, sed conidiis minoribus, (8–)9–10(–11) × Typus. AUSTRALIA, Northern Territory, Darwin, Charles Darwin University, (6–)6.5–7 µm, discernitur. S 12°22'25.2" E 130°52'07.4" on leaves of Hymenocallis littoralis (Amaryl lidaceae), 1 May 2011, P.W. Crous & M. Romberg, holotype CBS H-20759, Etymology. Named after the host genus from which it was isolated, cultures ex-type CPC 19332, 19331 = CBS 131309, ITS sequence GenBank Hymenocallis. JQ044423 and LSU sequence GenBank JQ044443, MycoBank MB560699; Associated with brown leaf spots and leaf tip blight. Conidio Darwin, in front of Vibe Hotel, Kitchener Drive, Darwin Conference Centre, on leaves of Hymenocallis littoralis, 27 Apr. 2011, P.W. Crous & B.A. Summerell, mata pycnidial, solitary, black, erumpent, globose, exuding CBS H-20760, cultures CPC 19330, 19329 = CBS 131310, ITS sequence colourless to opaque conidial masses; pycnidia up to 200 µm GenBank JQ044424. diam; pycnidial wall of several layers of brown textura angula ris, up to 30 µm thick; inner layer of hyaline textura angularis. Notes — During a meeting of the Australasian Society for Ostiole central, up to 20 µm diam, rim lined with darker brown Plant Pathology in Darwin (April 2011), a serious leaf spot and cells. Conidiophores subcylindrical to ampulliform, reduced tip blight disease was noticed on the Hymenocallis littoralis to conidiogenous cells, or with 1–2 supporting cells, at times plants growing in front of the conference centre. -
Figure 1. Bird Island: Physical Map, with Position of Tern Colony and Location of Vegetation Plots
Approximate of Sooty Ter~ Leqend (XI Vegetat~onplots 9 Building 6 Beach 200 metres Figure 1. Bird Island: Physical map, with position of tern colony and location of vegetation plots. BIRD MICHAEL J. HILL', TERENCE M. VEL', KATHRYN J. HOLM^, STEVEN J. PARR~ and NIRMAL J. SHAH' GEOLOGY, TOPOGRAPHY AND CLIMATE Bird is the northernmost island of the Seychelles, lying around 90 km north of Mahe, the largest of the granitic Seychelles, at the northern edge of the Seychelles bank. Different published sources vary in the estimated area of Bird Island with figures of c. 70 ha given by Feare (1979), 82 ha in Stoddart and Fosberg (1981), 101 ha in Skerrett et al. (2001), and 120.7 ha from recent aerial photographs (Ministry of Land Use and Habitat, Seychelles, unpublished data). In part, this variation may be explained by seasonal or longer-term variations in the vegetated area of the island; Bird Island is relatively dynamic, experiencing considerable coastal changes over time (Feare, 1979). The maximum elevation is less than 4 m above sea level. Unlike the majority of islands on the Seychelles Bank, Bird has no exposed granite and it is entirely formed of reef-derived sands. The accumulation of guano on sand deposits has led to the formation of phosphatic sandstone over 26% of the island's surface (Baker, 1963). Phosphatic sandstone is concentrated in a central band; the island's coastal zone is entirely sandy. Most of the original guano has now been removed for export. The soils of Bird Island are of two main series; over the central phosphatic sandstone area, Jemo series soils (missing their upper layer of guano) occur. -
Fleurs Et Arbres Des Seychelles
fleurs et arbres r~ des c§l#-~ SEYCHELLES OUVRAGE EDITE POUR LE COMPTE DU DEPARTEMENT DES FINANCES DES SEYCHELLES © 1986 Francis Friedmann et Département des Finances des Seychelles Toute reproduction, même partielle, par quelque procédé que ce soit, est rigoureusement interdite sans accord préalable de "Auteur et du Département des Finances des Seychelles, 2 fleurs et arbres r"~ des @/?-.... SEYCHELLES Texte et photos FRANCIS FRIEDMANN Office de la Recherche Scientifique et Technique Outre-Mer. (Pari~RSTOM Fonds Ducumt:llt ire N° ~ ~ O~ g rz. .0 o9 NOV. 1990 Cote e .-""----........... KENYA ,'" ...... " " .. " " .. 1" . 1 •• e. 1 1 ... 1 • • 1 ... 1 • 1 1 •• 1 • • MAHE " :. .,-.,-----.. ... " " • • L.LI ,'" ---- • Z " • « ZONE MARITIME ECONOMIQUE • N <," EXCLUSIVE DES SEYCHELLES Z \ « \\ 1- \\,.ALDABRA .. (",-------- "'" ••• 1 ,",. 1 , ...... " " 1 .. ',_--- --.... , ", :1 ~ ......... 1 ...... 1 4:) 0 ...... ) L.LI ...................' ::::l COMORES 0 o al ::E« No ::E REPUBLIQUE DES SEYCHELLES 4 .... ......, " \ "\ \ 1 1 1 1 ,1 , . ,, \ \ \ \ ,,\ ,, --------' OCEAN INDIEN Archipel central <:> ILE AUX VACHES DENIS ARIDE PETITE c::a SOEUR GRANDE SOEUR CURIEUSE ~ C> 0 ~ OFELICITE PRASLlN~ D tJMARIANNE ILE NORD ~ LA DIGUE <)SILHOUETTE ~FREGATE 5 PREFACE Les mers ~haudes, les plages dorées de sable fin, les récifs de coraux se retrouvent dans de nombreux pays sous les tropiques. Mais aucun d'entre eux ne peut se prévaloir à la fois d'une aussi grande richesse en plantes. oiseaux et animaux d'espèces rares, et d'un accueil aussi chaleureux que les Seychelles. Cet accueil se traduit tout aussi bien par la flore et la faune; le gouverne ment a fait preuve d'une initiative de pionnier en déclarant l'Océan Indien Zone Protégée en ce qui concerne les baleines et les dauphins. -
TELOPEA Publication Date: 13 October 1983 Til
Volume 2(4): 425–452 TELOPEA Publication Date: 13 October 1983 Til. Ro)'al BOTANIC GARDENS dx.doi.org/10.7751/telopea19834408 Journal of Plant Systematics 6 DOPII(liPi Tmst plantnet.rbgsyd.nsw.gov.au/Telopea • escholarship.usyd.edu.au/journals/index.php/TEL· ISSN 0312-9764 (Print) • ISSN 2200-4025 (Online) Telopea 2(4): 425-452, Fig. 1 (1983) 425 CURRENT ANATOMICAL RESEARCH IN LILIACEAE, AMARYLLIDACEAE AND IRIDACEAE* D.F. CUTLER AND MARY GREGORY (Accepted for publication 20.9.1982) ABSTRACT Cutler, D.F. and Gregory, Mary (Jodrell(Jodrel/ Laboratory, Royal Botanic Gardens, Kew, Richmond, Surrey, England) 1983. Current anatomical research in Liliaceae, Amaryllidaceae and Iridaceae. Telopea 2(4): 425-452, Fig.1-An annotated bibliography is presented covering literature over the period 1968 to date. Recent research is described and areas of future work are discussed. INTRODUCTION In this article, the literature for the past twelve or so years is recorded on the anatomy of Liliaceae, AmarylIidaceae and Iridaceae and the smaller, related families, Alliaceae, Haemodoraceae, Hypoxidaceae, Ruscaceae, Smilacaceae and Trilliaceae. Subjects covered range from embryology, vegetative and floral anatomy to seed anatomy. A format is used in which references are arranged alphabetically, numbered and annotated, so that the reader can rapidly obtain an idea of the range and contents of papers on subjects of particular interest to him. The main research trends have been identified, classified, and check lists compiled for the major headings. Current systematic anatomy on the 'Anatomy of the Monocotyledons' series is reported. Comment is made on areas of research which might prove to be of future significance. -
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. -
Identification and Characterization of Macrophomina Phaseolina Causing Leaf Blight on White Spider Lilies (Crinum Asiaticum and Hymenocallis Littoralis) in Malaysia
MYCOBIOLOGY 2019, VOL. 47, NO. 4, 408–414 https://doi.org/10.1080/12298093.2019.1682448 RESEARCH ARTICLE Identification and Characterization of Macrophomina phaseolina Causing Leaf Blight on White Spider Lilies (Crinum asiaticum and Hymenocallis littoralis) in Malaysia Abd Rahim Huda-Shakirah , Yee Jia Kee , Abu Bakar Mohd Hafifi , Nurul Nadiah Mohamad Azni, Latiffah Zakaria and Masratul Hawa Mohd School of Biological Sciences, Universiti Sains Malaysia, Penang, Malaysia ABSTRACT ARTICLE HISTORY Crinum asiaticum and Hymenocallis littoralis, commonly known as spider lilies are bulbous Received 11 March 2019 perennial and herbaceous plants that widely planted in Malaysia as ornamental. During Revised 3 August 2019 2015–2016, symptom of leaf blight was noticed on the hosts from several locations in Accepted 15 October 2019 Penang. The symptom appeared as irregular brown to reddish lesions surrounded by yellow KEYWORDS halos. As the disease progressed, the infected leaves became blighted, dried, and fell off Macrophomina phaseolina; with the presence of black microsclerotia and pycnidia on the lesions parts. The present leaf blight; Crinum study was conducted to investigate the causal pathogen of leaf blight on C. asiaticum and asiaticum; H. littoralis. Based on morphological characteristics and DNA sequences of internal tran- Hymenocallis littoralis scribed spacer (ITS) region and translation elongation factor 1-alpha (TEF1-a) gene, the causal pathogen was identified as Macrophomina phaseolina. Phylogenetic analysis of com- bined dataset of ITS and TEF1-a grouped the isolates studied with other isolates of M. pha- seolina from GenBank. The grouping of the isolates was supported by 96% bootstrap value. Pathogenicity test proved the role of the fungus in causing leaf blight on both hosts. -
Class Monocotyledonae
ACORUS/ACORACEAE 1077 CLASS MONOCOTYLEDONAE Plants usually herbaceous—in other words, lacking regular secondary thickening (except Palmaceae, Smilacaceae, most Agavaceae, and a few Poaceae); seedlings usually with 1 seed leaf or cotyledon; stems or branches elongating by apical growth and also by growth of basal por- tion of internodes; leaves when present alternate, whorled, basal, or rarely opposite, elongating by basal growth (readily seen on spring-flowering bulbs whose leaf-tips have been frozen back); leaf blades usually with parallel or concentrically curved veins, these unbranched or with inconspicuous, short, transverse connectives (leaves net-veined or with prominent midrib and spreading side-veins parallel with each other in Alismataceae, Araceae, Smilacaceae, Marantaceae, and some Orchidaceae); perianth with dissimilar inner and outer whorls (petals and sepals), or all parts about alike (tepals), the parianth parts separate or united, commonly in 3s, less often in 2s, rarely in 5s, or perianth of scales or bristles, or entirely absent. AWorldwide, the Monocotyledonae is a group composed of ca. 55,800 species in 2,652 genera arranged in 84 families (Mabberley 1997); 25 of these families occur in nc TX. The monocots appear to be a well-supported monophyletic group derived from within the monosulcate Magnoliidae group of dicots (Chase et al. 1993; Duvall et al. 1993; Qiu et al. 1993). From the cla- distic standpoint, the dicots are therefore paraphyletic and thus inappropriate for formal recog- nition (see explantion and Fig. 41 in Apendix 6). Within the monocots, Acorus appears to be the sister group to all other monocots, with the Alismataceae (and Potamogeton) being the next most basal group (Duvall et al. -
Networks in a Large-Scale Phylogenetic Analysis: Reconstructing Evolutionary History of Asparagales (Lilianae) Based on Four Plastid Genes
Networks in a Large-Scale Phylogenetic Analysis: Reconstructing Evolutionary History of Asparagales (Lilianae) Based on Four Plastid Genes Shichao Chen1., Dong-Kap Kim2., Mark W. Chase3, Joo-Hwan Kim4* 1 College of Life Science and Technology, Tongji University, Shanghai, China, 2 Division of Forest Resource Conservation, Korea National Arboretum, Pocheon, Gyeonggi- do, Korea, 3 Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, United Kingdom, 4 Department of Life Science, Gachon University, Seongnam, Gyeonggi-do, Korea Abstract Phylogenetic analysis aims to produce a bifurcating tree, which disregards conflicting signals and displays only those that are present in a large proportion of the data. However, any character (or tree) conflict in a dataset allows the exploration of support for various evolutionary hypotheses. Although data-display network approaches exist, biologists cannot easily and routinely use them to compute rooted phylogenetic networks on real datasets containing hundreds of taxa. Here, we constructed an original neighbour-net for a large dataset of Asparagales to highlight the aspects of the resulting network that will be important for interpreting phylogeny. The analyses were largely conducted with new data collected for the same loci as in previous studies, but from different species accessions and greater sampling in many cases than in published analyses. The network tree summarised the majority data pattern in the characters of plastid sequences before tree building, which largely confirmed the currently recognised phylogenetic relationships. Most conflicting signals are at the base of each group along the Asparagales backbone, which helps us to establish the expectancy and advance our understanding of some difficult taxa relationships and their phylogeny.