112 – April 2009 Newsletter
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Plant List 2016
Established 1990 PLANT LIST 2016 European mail order website www.crug-farm.co.uk CRÛG FARM PLANTS • 2016 Welcome to our 2016 list hope we can tempt you with plenty of our old favourites as well as some exciting new plants that we have searched out on our travels. There has been little chance of us standing still with what has been going on here in 2015. The year started well with the birth of our sixth grandchild. January into February had Sue and I in Colombia for our first winter/early spring expedition. It was exhilarating, we were able to travel much further afield than we had previously, as the mountainous areas become safer to travel. We are looking forward to working ever closer with the Colombian institutes, such as the Medellin Botanic Gardens whom we met up with. Consequently we were absent from the RHS February Show at Vincent Square. We are finding it increasingly expensive participating in the London shows, while re-branding the RHS February Show as a potato event hardly encourages our type of customer base to visit. A long standing speaking engagement and a last minute change of date, meant that we missed going to Fota near Cork last spring, no such problem this coming year. We were pleasantly surprised at the level of interest at the Trgrehan Garden Rare Plant Fair, in Cornwall. Hopefully this will become an annual event for us, as well as the Cornwall Garden Society show in April. Poor Sue went through the wars having to have a rush hysterectomy in June, after some timely results revealed future risks. -
New Plantings in the Arboretum the YEAR in REVIEW
Four new have been Four new Yoshino cherry trees have Yoshinobeen planted along planted Azalea Way. cherry trees along Azalea New Plantings in the Arboretum THE YEAR IN REVIEW T EX T B Y R AY L A R SON P HO T OS B Y N IA ll D UNNE n the five years that I have been curator, 2018 was the most active in terms of new plantings in the Arboretum. A majority of these centered around the new Arboretum Loop Trail and adjacent areas, many of which were enhanced, rehabilitated and Iaugmented. We also made improvements to a few other collection and garden areas with individual and smaller plantings. Following is a summary of some of the more noticeable new plantings you might encounter during your next visit. Winter 2019 v 3 Arboretum Entrance Perhaps the most obvious major planting occurred in March, just north of the Graham Visitors Center, with the creation of a new, large bed at the southeast corner of the intersection of Arboretum Drive and Foster Island Road. This intersection changed a lot as part of the Loop Trail construction—with the addition of new curbs and crosswalks—and we wanted to create a fitting entrance to the Arboretum at its north end. The new planting was also intended to alleviate some of the soil compaction and social trails that had developed on the east side of Arboretum Drive during trail construction. What’s more, we wanted to encourage pedes- trians to use the new gravel trail on the west side of the Drive to connect from the lower parking lots to the Visitors Center—rather than walk in the road. -
Well-Known Plants in Each Angiosperm Order
Well-known plants in each angiosperm order This list is generally from least evolved (most ancient) to most evolved (most modern). (I’m not sure if this applies for Eudicots; I’m listing them in the same order as APG II.) The first few plants are mostly primitive pond and aquarium plants. Next is Illicium (anise tree) from Austrobaileyales, then the magnoliids (Canellales thru Piperales), then monocots (Acorales through Zingiberales), and finally eudicots (Buxales through Dipsacales). The plants before the eudicots in this list are considered basal angiosperms. This list focuses only on angiosperms and does not look at earlier plants such as mosses, ferns, and conifers. Basal angiosperms – mostly aquatic plants Unplaced in order, placed in Amborellaceae family • Amborella trichopoda – one of the most ancient flowering plants Unplaced in order, placed in Nymphaeaceae family • Water lily • Cabomba (fanwort) • Brasenia (watershield) Ceratophyllales • Hornwort Austrobaileyales • Illicium (anise tree, star anise) Basal angiosperms - magnoliids Canellales • Drimys (winter's bark) • Tasmanian pepper Laurales • Bay laurel • Cinnamon • Avocado • Sassafras • Camphor tree • Calycanthus (sweetshrub, spicebush) • Lindera (spicebush, Benjamin bush) Magnoliales • Custard-apple • Pawpaw • guanábana (soursop) • Sugar-apple or sweetsop • Cherimoya • Magnolia • Tuliptree • Michelia • Nutmeg • Clove Piperales • Black pepper • Kava • Lizard’s tail • Aristolochia (birthwort, pipevine, Dutchman's pipe) • Asarum (wild ginger) Basal angiosperms - monocots Acorales -
BEDRI KARAKAS the Role of Sorbitol Synthesis in Photosynthesis of Peach (Prunus Persica) (Under the Direction of MARK W
BEDRI KARAKAS The role of sorbitol synthesis in photosynthesis of peach (Prunus persica) (Under the Direction of MARK W. RIEGER) This dissertation examines the hypothesis that polyol synthesis enhances photosynthetic capacity in peach and related species. Members of Prunus synthesize, translocate, and utilize sorbitol as their main photosynthetic end product whereas most other plants utilize sucrose for those purposes. First, I approached this hypothesis by examining eight genetically diverse Prunus species with various sorbitol: sucrose ratios and activities of sorbitol-6-phosphate dehydrogenase (S6PDH), principal sorbitol synthesis enzyme. Leaf photosynthetic capabilities (A), in vitro activity of the S6PDH and sorbitol contents of greenhouse grown plants were measured. I found an inverse relation between A and S6PDH activity of the species. This observation does not support the working hypothesis and that sorbitol synthesis enhances A. Second, I used two peach varieties (i.e., Encore and Nemaguard) to examine the same hypothesis within a single species by source/sink manipulations (i.e., fruiting versus non-fruiting, fruit present versus fruit removed, and shoot tip removal) and existing natural variation (i.e., leaf node position). In all cases, except fruiting versus non-fruiting and fruit present, photosynthesis and S6PDH enzyme activity showed positive correlations. Finally, I analyzed the response of S6PDH gene to shoot tip removal treatment in connection with S6PDH activity and A in potted Nemaguard peach plants. To document hourly changes, leaves were sampled three times during the day (i.e., sunrise, midday, and sunset) and analyzed for S6PDH gene expression and S6PDH activity. Sorbitol-6-phosphate dehydrogenase mRNA transcript levels significantly increased while S6PDH activity decreased 24-hour following shoot tip removal. -
Appendix 1: Maps and Plans Appendix184 Map 1: Conservation Categories for the Nominated Property
Appendix 1: Maps and Plans Appendix184 Map 1: Conservation Categories for the Nominated Property. Los Alerces National Park, Argentina 185 Map 2: Andean-North Patagonian Biosphere Reserve: Context for the Nominated Proprty. Los Alerces National Park, Argentina 186 Map 3: Vegetation of the Valdivian Ecoregion 187 Map 4: Vegetation Communities in Los Alerces National Park 188 Map 5: Strict Nature and Wildlife Reserve 189 Map 6: Usage Zoning, Los Alerces National Park 190 Map 7: Human Settlements and Infrastructure 191 Appendix 2: Species Lists Ap9n192 Appendix 2.1 List of Plant Species Recorded at PNLA 193 Appendix 2.2: List of Animal Species: Mammals 212 Appendix 2.3: List of Animal Species: Birds 214 Appendix 2.4: List of Animal Species: Reptiles 219 Appendix 2.5: List of Animal Species: Amphibians 220 Appendix 2.6: List of Animal Species: Fish 221 Appendix 2.7: List of Animal Species and Threat Status 222 Appendix 3: Law No. 19,292 Append228 Appendix 4: PNLA Management Plan Approval and Contents Appendi242 Appendix 5: Participative Process for Writing the Nomination Form Appendi252 Synthesis 252 Management Plan UpdateWorkshop 253 Annex A: Interview Guide 256 Annex B: Meetings and Interviews Held 257 Annex C: Self-Administered Survey 261 Annex D: ExternalWorkshop Participants 262 Annex E: Promotional Leaflet 264 Annex F: Interview Results Summary 267 Annex G: Survey Results Summary 272 Annex H: Esquel Declaration of Interest 274 Annex I: Trevelin Declaration of Interest 276 Annex J: Chubut Tourism Secretariat Declaration of Interest 278 -
Lamiaceae), with Emphasis on Taxonomic Implications
Biologia 67/5: 867—874, 2012 Section Botany DOI: 10.2478/s11756-012-0076-z Trichome micromorphology of the Chinese-Himalayan genus Colquhounia (Lamiaceae), with emphasis on taxonomic implications Guo-Xiong Hu1,3,TeodoraD.Balangcod2 & Chun-Lei Xiang1* 1Key Laboratory of Biodiversity and Biogeography, Kunming Institute of Botany, Chinese Academy of Sciences, 132 Lanhei Road, Heilongtan, Kunming 650201, Yunnan, P. R. China; e-mail: [email protected] 2Department of Biology, College of Science, University of the Philippines Baguio, 2600 Baguio City, Philippines 3Graduate School of Chinese Academy of Sciences, Beijing 100039,P.R.China Abstract: Trichome micromorphology of leaves and young stems of nine taxa (including four varieties) of Colquhounia were examined using light and scanning microscopy. Two basic types of trichomes were recognized: eglandular and glandular. Eglandular trichomes are subdivided into simple and branched trichomes. Based on the number of cells and trichome configuration, simple eglandular trichomes are further divided into four forms: unicellular, two-celled, three-celled and more than three-celled trichomes. Based on branching configuration, the branched eglandular trichomes can be separated into three forms: biramous, stellate and dendroid. Glandular trichomes can be divided into two subtypes: capitate and peltate glandular trichomes. Results from this study of morphological diversity of trichomes within Colquhounia lend insight into infrageneric classification and species relationships. Based on the presence of branched trichomes in C. elegans,thisspecies should be transferred from Colquhounia sect. Simplicipili to sect. Colquhounia. We provide a taxonomic key to species of Chinese Colquhounia based on trichome morphology and other important morphological traits. Key words: Colquhounia; glandular hairs; leaf anatomy; Lamioideae; Yunnan Introduction in spikes or capitula; equally 5–toothed calyces; and nutlets winged at apex (Li & Hedge 1994). -
Chile: a Journey to the End of the World in Search of Temperate Rainforest Giants
Eliot Barden Kew Diploma Course 53 July 2017 Chile: A Journey to the end of the world in search of Temperate Rainforest Giants Valdivian Rainforest at Alerce Andino Author May 2017 1 Eliot Barden Kew Diploma Course 53 July 2017 Table of Contents 1. Title Page 2. Contents 3. Table of Figures/Introduction 4. Introduction Continued 5. Introduction Continued 6. Aims 7. Aims Continued / Itinerary 8. Itinerary Continued / Objective / the Santiago Metropolitan Park 9. The Santiago Metropolitan Park Continued 10. The Santiago Metropolitan Park Continued 11. Jardín Botánico Chagual / Jardin Botanico Nacional, Viña del Mar 12. Jardin Botanico Nacional Viña del Mar Continued 13. Jardin Botanico Nacional Viña del Mar Continued 14. Jardin Botanico Nacional Viña del Mar Continued / La Campana National Park 15. La Campana National Park Continued / Huilo Huilo Biological Reserve Valdivian Temperate Rainforest 16. Huilo Huilo Biological Reserve Valdivian Temperate Rainforest Continued 17. Huilo Huilo Biological Reserve Valdivian Temperate Rainforest Continued 18. Huilo Huilo Biological Reserve Valdivian Temperate Rainforest Continued / Volcano Osorno 19. Volcano Osorno Continued / Vicente Perez Rosales National Park 20. Vicente Perez Rosales National Park Continued / Alerce Andino National Park 21. Alerce Andino National Park Continued 22. Francisco Coloane Marine Park 23. Francisco Coloane Marine Park Continued 24. Francisco Coloane Marine Park Continued / Outcomes 25. Expenditure / Thank you 2 Eliot Barden Kew Diploma Course 53 July 2017 Table of Figures Figure 1.) Valdivian Temperate Rainforest Alerce Andino [Photograph; Author] May (2017) Figure 2. Map of National parks of Chile Figure 3. Map of Chile Figure 4. Santiago Metropolitan Park [Photograph; Author] May (2017) Figure 5. -
M. C. Liberato, M. L. Caixinhas, M. Lousa & T. Vasconcelos
M. C. Liberato, M. L. Caixinhas, M. Lousa & T. Vasconcelos Mediterranean flora in some botanic gardens and parks in Portugal Abstract Liberato, M. C., Caixinhas, M. L., Lousà, M. & Vasconcelos, T.: Mediterranean flora in some botanic gardens and parks in Portugal. - Bocconea 16(2): 1123-1130.2003. - ISSN 1120-4060. In Portugal there are several remarkable botanic gardens and parks. The aim of this communi cation is to present some of the taxonomic studies don e by the authors in "Jardim-Museu Agricola Tropical" (Tropical Agricultural Museum-Garden), "Tapada da Ajuda" (Royal Park of Ajuda), "Parque da Pena" (Pena Park) and "Estufa Fria de Lisboa" (Cold Greenhouse of Lisbon). These spaces are located in Lisbon, except the Pena Park that is located in Sintra, near Lisbon. Ali these places have historical value. Plant collections of Mediterranean Region are kept in the above mentioned spaces. Species and the infraspecific taxa are indicated, as well their wild, some of their uses and their location in the mentioned areas. These Botanic Gardens and Parks are privileged spaces for the preservation of biodiversity ex sifu and in situo The potentiality to conserve species from several regions of the world, namely from the Mediterranean Region, makes these green spaces very important for research, as well as for didactic and educational programmes. Introduction In Portugal there are several botanic gardens and parks. This paper only concerns some Mediterranean species which grow in: "Jardim-Museu Agricola Tropical", "Tapada da Ajuda" and "Estufa Fria de Lisboa", these in Lisbon, and "Parque da Pena", in Sintra. Ali these spaces have historical value, and severa I research projects, inc\uding the phytotaxo nomic study of the above mentioned green areas, have been developed by the authors (Caixinhas 1994; Liberato 1994; Liberato & al. -
Preparing the Shaanxi-Qinling Mountains Integrated Ecosystem Management Project (Cofinanced by the Global Environment Facility)
Technical Assistance Consultant’s Report Project Number: 39321 June 2008 PRC: Preparing the Shaanxi-Qinling Mountains Integrated Ecosystem Management Project (Cofinanced by the Global Environment Facility) Prepared by: ANZDEC Limited Australia For Shaanxi Province Development and Reform Commission This consultant’s report does not necessarily reflect the views of ADB or the Government concerned, and ADB and the Government cannot be held liable for its contents. (For project preparatory technical assistance: All the views expressed herein may not be incorporated into the proposed project’s design. FINAL REPORT SHAANXI QINLING BIODIVERSITY CONSERVATION AND DEMONSTRATION PROJECT PREPARED FOR Shaanxi Provincial Government And the Asian Development Bank ANZDEC LIMITED September 2007 CURRENCY EQUIVALENTS (as at 1 June 2007) Currency Unit – Chinese Yuan {CNY}1.00 = US $0.1308 $1.00 = CNY 7.64 ABBREVIATIONS ADB – Asian Development Bank BAP – Biodiversity Action Plan (of the PRC Government) CAS – Chinese Academy of Sciences CASS – Chinese Academy of Social Sciences CBD – Convention on Biological Diversity CBRC – China Bank Regulatory Commission CDA - Conservation Demonstration Area CNY – Chinese Yuan CO – company CPF – country programming framework CTF – Conservation Trust Fund EA – Executing Agency EFCAs – Ecosystem Function Conservation Areas EIRR – economic internal rate of return EPB – Environmental Protection Bureau EU – European Union FIRR – financial internal rate of return FDI – Foreign Direct Investment FYP – Five-Year Plan FS – Feasibility -
Number 3, Spring 1998 Director’S Letter
Planning and planting for a better world Friends of the JC Raulston Arboretum Newsletter Number 3, Spring 1998 Director’s Letter Spring greetings from the JC Raulston Arboretum! This garden- ing season is in full swing, and the Arboretum is the place to be. Emergence is the word! Flowers and foliage are emerging every- where. We had a magnificent late winter and early spring. The Cornus mas ‘Spring Glow’ located in the paradise garden was exquisite this year. The bright yellow flowers are bright and persistent, and the Students from a Wake Tech Community College Photography Class find exfoliating bark and attractive habit plenty to photograph on a February day in the Arboretum. make it a winner. It’s no wonder that JC was so excited about this done soon. Make sure you check of themselves than is expected to seedling selection from the field out many of the special gardens in keep things moving forward. I, for nursery. We are looking to propa- the Arboretum. Our volunteer one, am thankful for each and every gate numerous plants this spring in curators are busy planting and one of them. hopes of getting it into the trade. preparing those gardens for The magnolias were looking another season. Many thanks to all Lastly, when you visit the garden I fantastic until we had three days in our volunteers who work so very would challenge you to find the a row of temperatures in the low hard in the garden. It shows! Euscaphis japonicus. We had a twenties. There was plenty of Another reminder — from April to beautiful seven-foot specimen tree damage to open flowers, but the October, on Sunday’s at 2:00 p.m. -
Newsletter No
The Irish Garden Plant Society Newsletter No. 133 September 2015 In this issue 1 Editorial 2 A word from the Chair 3 Myddelton House, the garden of E.A. Bowles by Dr. Mary Forrest 6 My memories of the Irish Gardeners’ Association by Thomas Byrne 13 The 34 th Annual General Meeting May 2015 18 Worth a read by Paddy Tobin 21 Notes on some Irish Plants by Paddy Tobin 24 Memories are made of plants by Carmel Duignan 26 Irish heritage plants update by Stephen Butler 27 Seed Distribution Scheme 2015/16 by Stephen Butler 28 Regional reports 34 A Wonderful Project – Plandaí Oidhreachta by Paddy Tobin 36 Aubrieta 'Shangarry' by Edel McDonald and Brendan Sayers 38 Details of upcoming events organised by the regional committees Front cover photograph of Escallonia ‘Glasnevin Hybrid’ courtesy of Pearse Rowe. This is one of a number of Escallonia cultivars raised by Charles Frederick Ball at Glasnevin where he worked as Assistant Keeper before joining the 7th Royal Dublin Fusiliers in World War l. Escallonia ‘Alice’ was named by Ball for his wife, he married in December 1914. The more widely available E. ‘C.F. Ball’ was named in his honour after his death; he died aged 36 years from shrapnel wounds at Gallipoli on 13 th September 1915. In his obituary he was described as “a delightful companion, unassuming, sincere and a most lovable man”. Editorial Dr. Mary Forrest on page 3 writes of a visit to Myddelton House London, the home of E. A. Bowles. In Moorea volume 15 Mary included in a list of horticultural trade organisations of the early 20 th century the Irish Gardeners’ Association. -
Gymnaconitum, a New Genus of Ranunculaceae Endemic to the Qinghai-Tibetan Plateau
TAXON 62 (4) • August 2013: 713–722 Wang & al. • Gymnaconitum, a new genus of Ranunculaceae Gymnaconitum, a new genus of Ranunculaceae endemic to the Qinghai-Tibetan Plateau Wei Wang,1 Yang Liu,2 Sheng-Xiang Yu,1 Tian-Gang Gao1 & Zhi-Duan Chen1 1 State Key Laboratory of Systematic and Evolutionary Botany, Institute of Botany, Chinese Academy of Sciences, Beijing 100093, P.R. China 2 Department of Ecology and Evolutionary Biology, University of Connecticut, Storrs, Connecticut 06269-3043, U.S.A. Author for correspondence: Wei Wang, [email protected] Abstract The monophyly of traditional Aconitum remains unresolved, owing to the controversial systematic position and taxonomic treatment of the monotypic, Qinghai-Tibetan Plateau endemic A. subg. Gymnaconitum. In this study, we analyzed two datasets using maximum likelihood and Bayesian inference methods: (1) two markers (ITS, trnL-F) of 285 Delphinieae species, and (2) six markers (ITS, trnL-F, trnH-psbA, trnK-matK, trnS-trnG, rbcL) of 32 Delphinieae species. All our analyses show that traditional Aconitum is not monophyletic and that subgenus Gymnaconitum and a broadly defined Delphinium form a clade. The SOWH tests also reject the inclusion of subgenus Gymnaconitum in traditional Aconitum. Subgenus Gymnaconitum markedly differs from other species of Aconitum and other genera of tribe Delphinieae in many non-molecular characters. By integrating lines of evidence from molecular phylogeny, divergence times, morphology, and karyology, we raise the mono- typic A. subg. Gymnaconitum to generic status. Keywords Aconitum; Delphinieae; Gymnaconitum; monophyly; phylogeny; Qinghai-Tibetan Plateau; Ranunculaceae; SOWH test Supplementary Material The Electronic Supplement (Figs. S1–S8; Appendices S1, S2) and the alignment files are available in the Supplementary Data section of the online version of this article (http://www.ingentaconnect.com/content/iapt/tax).