1 a Simple and Efficient Method of Germinating Cycad Seeds Bart Schutzman Environmental Horticulture Department, University of F
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Approved Plant List 10/04/12
FLORIDA The best time to plant a tree is 20 years ago, the second best time to plant a tree is today. City of Sunrise Approved Plant List 10/04/12 Appendix A 10/4/12 APPROVED PLANT LIST FOR SINGLE FAMILY HOMES SG xx Slow Growing “xx” = minimum height in Small Mature tree height of less than 20 feet at time of planting feet OH Trees adjacent to overhead power lines Medium Mature tree height of between 21 – 40 feet U Trees within Utility Easements Large Mature tree height greater than 41 N Not acceptable for use as a replacement feet * Native Florida Species Varies Mature tree height depends on variety Mature size information based on Betrock’s Florida Landscape Plants Published 2001 GROUP “A” TREES Common Name Botanical Name Uses Mature Tree Size Avocado Persea Americana L Bahama Strongbark Bourreria orata * U, SG 6 S Bald Cypress Taxodium distichum * L Black Olive Shady Bucida buceras ‘Shady Lady’ L Lady Black Olive Bucida buceras L Brazil Beautyleaf Calophyllum brasiliense L Blolly Guapira discolor* M Bridalveil Tree Caesalpinia granadillo M Bulnesia Bulnesia arboria M Cinnecord Acacia choriophylla * U, SG 6 S Group ‘A’ Plant List for Single Family Homes Common Name Botanical Name Uses Mature Tree Size Citrus: Lemon, Citrus spp. OH S (except orange, Lime ect. Grapefruit) Citrus: Grapefruit Citrus paradisi M Trees Copperpod Peltophorum pterocarpum L Fiddlewood Citharexylum fruticosum * U, SG 8 S Floss Silk Tree Chorisia speciosa L Golden – Shower Cassia fistula L Green Buttonwood Conocarpus erectus * L Gumbo Limbo Bursera simaruba * L -
Chemical Element Concentrations of Cycad Leaves: Do We Know Enough?
horticulturae Review Chemical Element Concentrations of Cycad Leaves: Do We Know Enough? Benjamin E. Deloso 1 , Murukesan V. Krishnapillai 2 , Ulysses F. Ferreras 3, Anders J. Lindström 4, Michael Calonje 5 and Thomas E. Marler 6,* 1 College of Natural and Applied Sciences, University of Guam, Mangilao, GU 96923, USA; [email protected] 2 Cooperative Research and Extension, Yap Campus, College of Micronesia-FSM, Colonia, Yap 96943, Micronesia; [email protected] 3 Philippine Native Plants Conservation Society Inc., Ninoy Aquino Parks and Wildlife Center, Quezon City 1101, Philippines; [email protected] 4 Plant Collections Department, Nong Nooch Tropical Botanical Garden, 34/1 Sukhumvit Highway, Najomtien, Sattahip, Chonburi 20250, Thailand; [email protected] 5 Montgomery Botanical Center, 11901 Old Cutler Road, Coral Gables, FL 33156, USA; [email protected] 6 Western Pacific Tropical Research Center, University of Guam, Mangilao, GU 96923, USA * Correspondence: [email protected] Received: 13 October 2020; Accepted: 16 November 2020; Published: 19 November 2020 Abstract: The literature containing which chemical elements are found in cycad leaves was reviewed to determine the range in values of concentrations reported for essential and beneficial elements. We found 46 of the 358 described cycad species had at least one element reported to date. The only genus that was missing from the data was Microcycas. Many of the species reports contained concentrations of one to several macronutrients and no other elements. The cycad leaves contained greater nitrogen and phosphorus concentrations than the reported means for plants throughout the world. Magnesium was identified as the macronutrient that has been least studied. -
The Supramolecular Organization of Self-Assembling Chlorosomal Bacteriochlorophyll C, D,Ore Mimics
The supramolecular organization of self-assembling chlorosomal bacteriochlorophyll c, d,ore mimics Tobias Jochum*†, Chilla Malla Reddy†‡, Andreas Eichho¨ fer‡, Gernot Buth*, Je¸drzej Szmytkowski§¶, Heinz Kalt§¶, David Moss*, and Teodor Silviu Balaban‡¶ʈ *Institute for Synchrotron Radiation, Karlsruhe Institute of Technology, Forschungszentrum Karlsruhe, Postfach 3640, D-76021 Karlsruhe, Germany; ‡Institute for Nanotechnology, Karlsruhe Institute of Technology, Forschungszentrum Karlsruhe, Postfach 3640, D-76021 Karlsruhe, Germany; §Institute of Applied Physics, Karlsruhe Institute of Technology, Universita¨t Karlsruhe (TH), D-76131 Karslruhe, Germany; and ¶Center for Functional Nanostructures, Universita¨t Karlsruhe (TH), D-76131 Karslruhe, Germany Edited by James R. Norris, University of Chicago, Chicago, IL, and accepted by the Editorial Board July 18, 2008 (received for review March 22, 2008) Bacteriochlorophylls (BChls) c, d, and e are the main light-harvesting direct structural evidence from x-ray single crystal structures, the pigments of green photosynthetic bacteria that self-assemble into exact nature of BChl superstructures remain elusive and these nanostructures within the chlorosomes forming the most efficient have been controversially discussed in the literature (1–3, 7, antennas of photosynthetic organisms. All previous models of the 11–17). It is now generally accepted that the main feature of chlorosomal antennae, which are quite controversially discussed chlorosomes is the self-assembly of BChls and that these pig- because no single crystals could be grown so far from these or- ments are not bound by a rigid protein matrix as is the case of ganelles, involve a strong hydrogen-bonding interaction between the other, well characterized light-harvesting systems (1). Small- 31 hydroxyl group and the 131 carbonyl group. -
Cycad Forensics: Tracing the Origin of Poached Cycads Using Stable Isotopes, Trace Element Concentrations and Radiocarbon Dating Techniques
Cycad forensics: Tracing the origin of poached cycads using stable isotopes, trace element concentrations and radiocarbon dating techniques by Kirsten Retief Supervisors: Dr Adam West (UCT) and Ms Michele Pfab (SANBI) Submitted in partial fulfillment of the requirements for the degree of Masters of Science in Conservation Biology 5 June 2013 Percy FitzPatrick Institution of African Ornithology, UniversityDepartment of Biologicalof Cape Sciences Town University of Cape Town, Rondebosch Cape Town South Africa 7701 i The copyright of this thesis vests in the author. No quotation from it or information derived from it is to be published without full acknowledgement of the source. The thesis is to be used for private study or non- commercial research purposes only. Published by the University of Cape Town (UCT) in terms of the non-exclusive license granted to UCT by the author. University of Cape Town Table of Contents Acknowledgements iii Plagiarism declaration iv Abstract v Chapter 1: Status of cycads and background to developing a forensic technique 1 1. Why are cycads threatened? 2 2. Importance of cycads 4 3. Current conservation strategies 5 4. Stable isotopes in forensic science 7 5. Trace element concentrations 15 6. Principles for using isotopes as a tracer 15 7. Radiocarbon dating 16 8. Cycad life history, anatomy and age of tissues 18 9. Recapitulation 22 Chapter 2: Applying stable isotope and radiocarbon dating techniques to cycads 23 1. Introduction 24 2. Methods 26 2.1 Sampling selection and sites 26 2.2 Sampling techniques 30 2.3 Processing samples 35 2.4 Cellulose extraction 37 2.5 Oxygen and sulphur stable isotopes 37 2.6 CarbonUniversity and nitrogen stable of isotopes Cape Town 38 2.7 Strontium, lead and elemental concentration analysis 39 2.8 Radiocarbon dating 41 2.9 Data analysis 42 3. -
Cycas Revoluta1
Fact Sheet FPS-162 October, 1999 Cycas revoluta1 Edward F. Gilman2 Introduction The palm-like King Sago has a short, dark brown, unbranching trunk topped with graceful, arching, dark green, feathery leaves, two to three feet long (Fig. 1). King Sago is not a palm tree. It will eventually reach to about eight feet tall, but grows about one or two inches per year. The individual leaflets each end in a sharp tip. Although very slow-growing, King Sago is much prized for its tropical effect and easy care and makes an excellent specimen or container plant. It is easy to grow as a house plant. General Information Scientific name: Cycas revoluta Pronunciation: SYE-kus rev-voe-LOO-tuh Common name(s): King Sago Family: Cycadaceae Plant type: shrub USDA hardiness zones: 8B through 11 (Fig. 2) Planting month for zone 8: year round Planting month for zone 9: year round Figure 1. King Sago. Planting month for zone 10 and 11: year round Origin: not native to North America Uses: container or above-ground planter; border; mass Description planting; accent; suitable for growing indoors Height: 3 to 10 feet Availablity: somewhat available, may have to go out of the Spread: 4 to 8 feet region to find the plant Plant habit: palm Plant density: moderate Growth rate: slow Texture: fine 1.This document is Fact Sheet FPS-162, one of a series of the Environmental Horticulture Department, Florida Cooperative Extension Service, Institute of Food and Agricultural Sciences, University of Florida. Publication date: October 1999. Please visit the EDIS web site at http://edis.ifas.ufl.edu. -
Comparative Biology of Cycad Pollen, Seed and Tissue - a Plant Conservation Perspective
Bot. Rev. (2018) 84:295–314 https://doi.org/10.1007/s12229-018-9203-z Comparative Biology of Cycad Pollen, Seed and Tissue - A Plant Conservation Perspective J. Nadarajan1,2 & E. E. Benson 3 & P. Xaba 4 & K. Harding3 & A. Lindstrom5 & J. Donaldson4 & C. E. Seal1 & D. Kamoga6 & E. M. G. Agoo7 & N. Li 8 & E. King9 & H. W. Pritchard1,10 1 Royal Botanic Gardens, Kew, Wakehurst Place, Ardingly, West Sussex RH17 6TN, UK; e-mail: [email protected] 2 The New Zealand Institute for Plant & Food Research Ltd, Private Bag 11600, Palmerston North 4442, New Zealand; e-mail [email protected] 3 Damar Research Scientists, Damar, Cuparmuir, Fife KY15 5RJ, UK; e-mail: [email protected]; [email protected] 4 South African National Biodiversity Institute, Kirstenbosch National Botanical Garden, Cape Town, Republic of South Africa; e-mail: [email protected]; [email protected] 5 Nong Nooch Tropical Botanical Garden, Chonburi 20250, Thailand; e-mail: [email protected] 6 Joint Ethnobotanical Research Advocacy, P.O.Box 27901, Kampala, Uganda; e-mail: [email protected] 7 De La Salle University, Manila, Philippines; e-mail: [email protected] 8 Fairy Lake Botanic Garden, Shenzhen, Guangdong, People’s Republic of China; e-mail: [email protected] 9 UNEP-World Conservation Monitoring Centre, Cambridge, UK; e-mail: [email protected] 10 Author for Correspondence; e-mail: [email protected] Published online: 5 July 2018 # The Author(s) 2018 Abstract Cycads are the most endangered of plant groups based on IUCN Red List assessments; all are in Appendix I or II of CITES, about 40% are within biodiversity ‘hotspots,’ and the call for action to improve their protection is long- standing. -
Part IX – Appendices
Monterey Bay National Marine Sanctuary – Proposed Action Plans Part IX – Appendices Monterey Bay Sanctuary Advisory Council Membership List of Acronyms 445 Monterey Bay National Marine Sanctuary – Proposed Action Plans Appendix 1 – Sanctuary Advisory Council Membership Non-Governmental Members ------------------------------------------------------------------------ Agriculture (Primary & SAC Vice Chair) Mr. Richard Nutter [email protected] ------------------------------------------------------------------------ Agriculture (Alternate) Mr. Kirk Schmidt Quail Mountain Herbs 831-722-8456 [email protected] ------------------------------------------------------------------------ Business/Industry (Primary) Mr. Dave Ebert, Ph.D. Project Manager, Pacific Shark Research Center 831-771-4427 [email protected] or [email protected] ------------------------------------------------------------------------ Business/Industry (Alternate) Mr. Tony Warman 831-462-4059 [email protected] ------------------------------------------------------------------------ Conservation (Primary) Ms. Vicki Nichols Director of Research & Policy Save Our Shores 831-462-5660 [email protected] ------------------------------------------------------------------------ Conservation (Alternate) Ms. Kaitilin Gaffney Central Coast Program Director The Ocean Conservancy 831-425-1363 [email protected] ------------------------------------------------------------------------ Diving (Primary) Mr. Frank Degnan CSUMB [email protected] ------------------------------------------------------------------------ -
Seedless Plants Key Concept Seedless Plants Do Not Produce Seeds 2 but Are Well Adapted for Reproduction and Survival
Seedless Plants Key Concept Seedless plants do not produce seeds 2 but are well adapted for reproduction and survival. What You Will Learn When you think of plants, you probably think of plants, • Nonvascular plants do not have such as trees and flowers, that make seeds. But two groups of specialized vascular tissues. plants don’t make seeds. The two groups of seedless plants are • Seedless vascular plants have specialized vascular tissues. nonvascular plants and seedless vascular plants. • Seedless plants reproduce sexually and asexually, but they need water Nonvascular Plants to reproduce. Mosses, liverworts, and hornworts do not have vascular • Seedless plants have two stages tissue to transport water and nutrients. Each cell of the plant in their life cycle. must get water from the environment or from a nearby cell. So, Why It Matters nonvascular plants usually live in places that are damp. Also, Seedless plants play many roles in nonvascular plants are small. They grow on soil, the bark of the environment, including helping to form soil and preventing erosion. trees, and rocks. Mosses, liverworts, and hornworts don’t have true stems, roots, or leaves. They do, however, have structures Vocabulary that carry out the activities of stems, roots, and leaves. • rhizoid • rhizome Mosses Large groups of mosses cover soil or rocks with a mat of Graphic Organizer In your Science tiny green plants. Mosses have leafy stalks and rhizoids. A Journal, create a Venn Diagram that rhizoid is a rootlike structure that holds nonvascular plants in compares vascular plants and nonvas- place. Rhizoids help the plants get water and nutrients. -
Proliferated Megasporangiate Strobili of Zamia Furfuracea (Zamiaceae, Cycadales) and Its Possible Evolutionary Implications for the Origin of Cycad-Megasporophylls
Palaeodiversity 6: 135–147; Stuttgart, 30 December 2013. 135 Proliferated megasporangiate strobili of Zamia furfuracea (Zamiaceae, Cycadales) and its possible evolutionary implications for the origin of cycad-megasporophylls VEIT MARTIN DÖRKEN & BRIGITTE ROZYNEK Abstract At a 30-years-old individual of Zamia furfuracea (Zamiaceae, Cycadales) cultivated in the Botanic Garden Bo- chum (Germany), several proliferated megasporangiate strobili were found. The morphology of normal and prolif- erated strobili was compared. Within the proliferated strobili the sequence of megasporophylls, cataphylls, tropho- phyll-like leaves, followed again by a flush of cataphylls, was similar to those developed at the stems of extant Cycas species. However, all proliferated megasporangiate strobili were sterile. Within the proliferated strobili the pinnate trophophyll-like leaves that were replacing the terminal megasporophylls can be regarded as an atavism possibly reflecting the primitive character of megasporophylls in cycads. Thus, the results of the morphological examinations and also the comparison with fossil taxa may deliver new data supporting the idea that pinnate cycad-megasporo- phylls are a plesiomorphic feature within cycads. Keywords: Zamia, Cycadales, strobilus, megasporophyll, proliferation. 1. Introduction often wedge-shaped with a hexagonal outer face. In some species they have one or two distal spine-like appendages. Due to the morphology of megasporangiate strobili, me- Each megasporophyll bears only two ovules, which are gasporophylls and the attachment of ovules, the systemat- developed deeply within the strobilus. The micropyles are ics among extant cycads is still debated. Some authors sug- pointing towards the axis of the strobilus. gest a concept composing of three families: Cycadaceae, In contrast with the Zamiaceae, among the Cycadaceae Stangeriaceae, and Zamiaceae (e.g. -
The Relationship Between Moss Growth and Treefall Gaps
The Relationship between Moss Growth and Treefall Gaps BIOS 35502-01 Practicum in Field Biology Leah Ellman Advisor: Dr. Walter Carson Abstract: Mosses are a rarely studied component of treefall gaps in forest ecosystems – and ought to receive more attention due to their potential to promote or deter vascular seedling germination and survival. The aim of this study, therefore, was to determine if there is a relationship between canopy gaps and moss growth along forest floors and to determine if there is a difference between the effect of canopy gaps on the depth and abundance of acrocarpous versus pleurocarpous mosses. The study took place in an eastern deciduous forest biome on the University of Notre Dame Environmental Research (UNDERC) property located between upper Michigan and Wisconsin. I paired treefall gap and closed canopy plots along bog border habitat and ran a single transect from east to west in all plots. I then recorded the number of moss beds, as well as bed depth(s), and moss type (acrocarpous/pleurocarpous) within a half meter of either side of the transects. Afterwards, I analyzed the data via regressions and paired t-tests, and found that while canopy gaps have no significant effect on moss depth, moss abundance was positively related to treefall gap presence. Introduction: Treefall gaps are key promoters of plant diversity in forest ecosystems. They are caused by disturbances such as windstorms and result in increased light availability on the forest floor which promotes the growth of shade intolerant plants and maintains forest diversity (Schnitzer and Carson, 2001; Spies and Franklin 1989; Brokaw, 1985; Brokaw, 1987; Abe et al. -
Strictly Dioecious Plant Vegetative
Bhagalpur National College, Bhagalpur ( A Constituent unit of Tilka Manjhi Bhagalpur University, Bhagalpur) PPT Presentation for B.Sc. I- CYCAS: Structure, Reproduction and Life cycle Presented by - Dr. Amit Kishore Singh Department of Botany B.N. College, Bhagalpur Distribution and Occurence . It includes 20 species. Occurs wild or cultivated in tropical and sub-tropical regions. South of Eastern Hemisphere • e.g. S. Japan, India, China, N. Australia, E. Coasts of Africa, Myanmar, Bangladesh, Mauritius, Nepal, etc. It is evergreen plant in India represented with 6 species- Cycas revoluta, C. pectinata, C. siamensis, C. beddomei, C. rumphi and C. Circinali. The plants grow in xerophytic conditions. It is cultivated as ornamental plant in the garden. Cycas is called a living fossil. Cycas revoluta (sago palm) Cycas rumphi (false sago) Cycas circinalis (queen sago) Cycas siamensis Cycas pectinata Cycas beddomei Morphology Sporophyte is dioecious i.e. male and female plants are separate. Plant body is differentiated into roots, stem and leaves. Roots • Roots are of two types – normal root Stem and coralloid roots. • Root hairs and rot cap are absent. Root • Normal roots helps in absorption and anchorage. • Coralloid roots helps in nitrogen fixation. Stem is erect, columnar, woody and unbranched, covered with alternate whorls of leaf bases of foliage and scaly leaves. Foliage or assimilatory leaves (1-3 mm, green, pinnately compund, photosynthetic Leaves are dimorphic – in nature) Scaly leaves or cataphylls (small, dry, brown, triangular leaves covered with ramenta, photosynthetic in nature, protect the stem apex) Cycas leaf Internal structure T. S of coralloid roots 1. It is circular in outline and the T. -
Elemental Profiles in Cycas Micronesica Stems
plants Article Elemental Profiles in Cycas micronesica Stems Thomas E. Marler College of Natural and Applied Sciences, University of Guam, UOG Station, Mangilao, Guam 96923, USA; [email protected]; Tel.: +1-671-735-2100 Received: 24 August 2018; Accepted: 30 October 2018; Published: 1 November 2018 Abstract: Essential nutrients and metals have been quantified in stems of many tree species to understand the role of stems as storage and source organs. Little is known about stored stem resources of cycad tree species. Cycas micronesica tissue was collected from apical and basal axial regions of stems; and pith, vascular, and cortex tissues were separated into three radial regions. Leaves were also sampled to provide a comparison to stems. Minerals and metals were quantified in all tissues. Minerals and metals varied greatly among the six stem sections. Phosphorus varied more among the three radial sections than the other macronutrients, and zinc and nickel varied more than the other micronutrients. Stem carbon was less than and stem calcium was greater than expected, based on what is currently known tree stem concentrations in the literature. Elemental concentrations were generally greater than those previously reported for coniferous gymnosperm trees. Moreover, the stem concentrations were high in relation to leaf concentrations, when compared to published angiosperm and conifer data. The results indicated that the addition of more cycad species to the literature will improve our understanding of gymnosperm versus angiosperm stem nutrient relations, and that the non-woody cycad stem contains copious essential plant nutrients that can be mobilized and deployed to sinks when needed.