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Toward a Resolution of Campanulid Phylogeny, with Special Reference to the Placement of Dipsacales
TAXON 57 (1) • February 2008: 53–65 Winkworth & al. • Campanulid phylogeny MOLECULAR PHYLOGENETICS Toward a resolution of Campanulid phylogeny, with special reference to the placement of Dipsacales Richard C. Winkworth1,2, Johannes Lundberg3 & Michael J. Donoghue4 1 Departamento de Botânica, Instituto de Biociências, Universidade de São Paulo, Caixa Postal 11461–CEP 05422-970, São Paulo, SP, Brazil. [email protected] (author for correspondence) 2 Current address: School of Biology, Chemistry, and Environmental Sciences, University of the South Pacific, Private Bag, Laucala Campus, Suva, Fiji 3 Department of Phanerogamic Botany, The Swedish Museum of Natural History, Box 50007, 104 05 Stockholm, Sweden 4 Department of Ecology & Evolutionary Biology and Peabody Museum of Natural History, Yale University, P.O. Box 208106, New Haven, Connecticut 06520-8106, U.S.A. Broad-scale phylogenetic analyses of the angiosperms and of the Asteridae have failed to confidently resolve relationships among the major lineages of the campanulid Asteridae (i.e., the euasterid II of APG II, 2003). To address this problem we assembled presently available sequences for a core set of 50 taxa, representing the diver- sity of the four largest lineages (Apiales, Aquifoliales, Asterales, Dipsacales) as well as the smaller “unplaced” groups (e.g., Bruniaceae, Paracryphiaceae, Columelliaceae). We constructed four data matrices for phylogenetic analysis: a chloroplast coding matrix (atpB, matK, ndhF, rbcL), a chloroplast non-coding matrix (rps16 intron, trnT-F region, trnV-atpE IGS), a combined chloroplast dataset (all seven chloroplast regions), and a combined genome matrix (seven chloroplast regions plus 18S and 26S rDNA). Bayesian analyses of these datasets using mixed substitution models produced often well-resolved and supported trees. -
The Vegetation of Robinson Crusoe Island (Isla Masatierra), Juan
The Vegetation ofRobinson Crusoe Island (Isla Masatierra), Juan Fernandez Archipelago, Chile1 Josef Greimler,2,3 Patricio Lopez 5., 4 Tod F. Stuessy, 2and Thomas Dirnbiick5 Abstract: Robinson Crusoe Island of the Juan Fernandez Archipelago, as is the case with many oceanic islands, has experienced strong human disturbances through exploitation ofresources and introduction of alien biota. To understand these impacts and for purposes of diversity and resource management, an accu rate assessment of the composition and structure of plant communities was made. We analyzed the vegetation with 106 releves (vegetation records) and subsequent Twinspan ordination and produced a detailed colored map at 1: 30,000. The resultant map units are (1) endemic upper montane forest, (2) endemic lower montane forest, (3) Ugni molinae shrubland, (4) Rubus ulmifolius Aristotelia chilensis shrubland, (5) fern assemblages, (6) Libertia chilensis assem blage, (7) Acaena argentea assemblage, (8) native grassland, (9) weed assemblages, (10) tall ruderals, and (11) cultivated Eucalyptus, Cupressus, and Pinus. Mosaic patterns consisting of several communities are recognized as mixed units: (12) combined upper and lower montane endemic forest with aliens, (13) scattered native vegetation among rocks at higher elevations, (14) scattered grassland and weeds among rocks at lower elevations, and (15) grassland with Acaena argentea. Two categories are included that are not vegetation units: (16) rocks and eroded areas, and (17) settlement and airfield. Endemic forests at lower elevations and in drier zones of the island are under strong pressure from three woody species, Aristotelia chilensis, Rubus ulmifolius, and Ugni molinae. The latter invades native forests by ascending dry slopes and ridges. -
Fair Use of This PDF File of Herbaceous
Fair Use of this PDF file of Herbaceous Perennials Production: A Guide from Propagation to Marketing, NRAES-93 By Leonard P. Perry Published by NRAES, July 1998 This PDF file is for viewing only. If a paper copy is needed, we encourage you to purchase a copy as described below. Be aware that practices, recommendations, and economic data may have changed since this book was published. Text can be copied. The book, authors, and NRAES should be acknowledged. Here is a sample acknowledgement: ----From Herbaceous Perennials Production: A Guide from Propagation to Marketing, NRAES- 93, by Leonard P. Perry, and published by NRAES (1998).---- No use of the PDF should diminish the marketability of the printed version. This PDF should not be used to make copies of the book for sale or distribution. If you have questions about fair use of this PDF, contact NRAES. Purchasing the Book You can purchase printed copies on NRAES’ secure web site, www.nraes.org, or by calling (607) 255-7654. Quantity discounts are available. NRAES PO Box 4557 Ithaca, NY 14852-4557 Phone: (607) 255-7654 Fax: (607) 254-8770 Email: [email protected] Web: www.nraes.org More information on NRAES is included at the end of this PDF. Acknowledgments This publication is an update and expansion of the 1987 Cornell Guidelines on Perennial Production. Informa- tion in chapter 3 was adapted from a presentation given in March 1996 by John Bartok, professor emeritus of agricultural engineering at the University of Connecticut, at the Connecticut Perennials Shortcourse, and from articles in the Connecticut Greenhouse Newsletter, a publication put out by the Department of Plant Science at the University of Connecticut. -
Evaluation of a Proposed Significant Natural Area at Mt Iron, Wanaka
EVALUATION OF A PROPOSED SIGNIFICANT NATURAL AREA AT MT IRON, WANAKA R3762 EVALUATION OF A PROPOSED SIGNIFICANT NATURAL AREA AT MT IRON, WANAKA Coprosma shrubland on the southwest faces at the Allenby Farms site, Mt Iron. Contract Report No. 3762 March 2017 (Revised and updated) Project Team: Kelvin Lloyd - Report author: vegetation and flora Mandy Tocher - Report author: herpetofauna Brian Patrick - Report author: invertebrates Prepared for: Allenby Farms Ltd P.O. Box 196 Wanaka 9343 DUNEDIN OFFICE: 764 CUMBERLAND STREET, DUNEDIN 9016 Ph 03-477-2096, 03-477-2095 HEAD OFFICE: 99 SALA STREET, P.O. BOX 7137, TE NGAE, ROTORUA Ph 07-343-9017, 07-343-9018; email [email protected], www.wildlands.co.nz CONTENTS 1. INTRODUCTION 1 2. SITE CONTEXT 1 3. METHODS 1 4. ECOLOGICAL CONTEXT 4 5. INDIGENOUS VEGETATION AND HABITATS 5 5.1 Kānuka scrub and shrubland 5 5.2 Coprosma scrub and shrubland 6 5.3 Exotic grassland and herbfield 7 5.4 Swale turf 8 5.5 Cushionfield 8 6. FLORA 8 6.1 Species richness 8 6.2 Threatened and At Risk plant species 12 6.3 Pest plants 12 7. BIRDS 13 8. LIZARDS 14 8.1 Overview 14 8.2 “Remove from SNA” zone 14 8.3 Alternate SNA 18 9. INVERTEBRATES 18 9.1 Overview 18 9.2 Mixed Coprosma-dominant shrubland 18 9.3 Kānuka scrub and shrubland 19 9.4 Rock outcrop habitats 19 9.5 Open grassland and turf 19 10. PEST ANIMALS 20 11. ECOLOGICAL VALUES 20 11.1 District Plan (2009) - Section 6c Significance 20 11.2 Proposed District Plan - Section 6c Significance from Policy 33.2.1.9 22 11.3 Significance summary 23 12. -
Metrosideros Carminea
Metrosideros carminea COMMON NAME Carmine rata SYNONYMS Metrosideros diffusa Hook.f. FAMILY Myrtaceae AUTHORITY Metrosideros carminea W.R.B.Oliv. FLORA CATEGORY Vascular – Native ENDEMIC TAXON Yes ENDEMIC GENUS Carmine rata. Photographer: DoC No ENDEMIC FAMILY No STRUCTURAL CLASS Lianes & Related Trailing Plants - Dicotyledons NVS CODE METCAR CHROMOSOME NUMBER 2n = 22 CURRENT CONSERVATION STATUS 2018 | Threatened – Nationally Vulnerable PREVIOUS CONSERVATION STATUSES 2012 | Not Threatened 2009 | Not Threatened 2004 | Not Threatened Metrosideros carminea. Photographer: Peter de BRIEF DESCRIPTION Lange Woody long-climbing vine. Mature plants only reproductive. Juvenile foliage hairy, with young growth often pinkish. Adult leaves more or less circular, dark glossy green above, pale green below, surfaces without any obvious glandular spotting. Flowers carmine borne in dense, terminal, fluffy, clusters. DISTRIBUTION Endemic. New Zealand: North Island (from Te Paki south to Taranaki in the west and Mahia Peninsula in the east) HABITAT Coastal to montane (mainly coastal to lowland). A vine of closed forest and forest margins (often along water ways and on ridge lines, especially on rock outcrops and cliff faces). FEATURES Vine up to 15 m (usually less). Bark dark brown to grey, ± tessellated, and flaking in tabular shards. Growth dimorphic, juvenile and climbing vines sparingly branched, mature (adult - reproductive state) heavily branched. Branchlets terete, finely pubescent. Leaves, close-set, coriaceous, petiolate; petioles 1-3 mm. long; lamina of juveniles 10-20 × 8-18 mm, suborbicular, orbicular to broadly ovate, apices obtuse to subacute; adaxially green to dark green, abaxially paler (young foliage (and branchlet growing points) usually pink-tinged), both surfaces finely to distinctly pubescent, hairs pinkish, oil glands conspicuous abaxially not punctate,; adult lamina 15-35 × 7-30 mm, elliptic-oblong, ovate-oblong to broad ovate, apices obtuse to subacute, adaxially dark green and glossy, adaxially paler, ± glossy, ± glabrous. -
Environmental Weeds of Coastal Plains and Heathy Forests Bioregions of Victoria Heading in Band
Advisory list of environmental weeds of coastal plains and heathy forests bioregions of Victoria Heading in band b Advisory list of environmental weeds of coastal plains and heathy forests bioregions of Victoria Heading in band Advisory list of environmental weeds of coastal plains and heathy forests bioregions of Victoria Contents Introduction 1 Purpose of the list 1 Limitations 1 Relationship to statutory lists 1 Composition of the list and assessment of taxa 2 Categories of environmental weeds 5 Arrangement of the list 5 Column 1: Botanical Name 5 Column 2: Common Name 5 Column 3: Ranking Score 5 Column 4: Listed in the CALP Act 1994 5 Column 5: Victorian Alert Weed 5 Column 6: National Alert Weed 5 Column 7: Weed of National Significance 5 Statistics 5 Further information & feedback 6 Your involvement 6 Links 6 Weed identification texts 6 Citation 6 Acknowledgments 6 Bibliography 6 Census reference 6 Appendix 1 Environmental weeds of coastal plains and heathy forests bioregions of Victoria listed alphabetically within risk categories. 7 Appendix 2 Environmental weeds of coastal plains and heathy forests bioregions of Victoria listed by botanical name. 19 Appendix 3 Environmental weeds of coastal plains and heathy forests bioregions of Victoria listed by common name. 31 Advisory list of environmental weeds of coastal plains and heathy forests bioregions of Victoria i Published by the Victorian Government Department of Sustainability and Environment Melbourne, March2008 © The State of Victoria Department of Sustainability and Environment 2009 This publication is copyright. No part may be reproduced by any process except in accordance with the provisions of the Copyright Act 1968. -
(A) Journals with the Largest Number of Papers Reporting Estimates Of
Supplementary Materials Figure S1. (a) Journals with the largest number of papers reporting estimates of genetic diversity derived from cpDNA markers; (b) Variation in the diversity (Shannon-Wiener index) of the journals publishing studies on cpDNA markers over time. Figure S2. (a) The number of publications containing estimates of genetic diversity obtained using cpDNA markers, in relation to the nationality of the corresponding author; (b) The number of publications on genetic diversity based on cpDNA markers, according to the geographic region focused on by the study. Figure S3. Classification of the angiosperm species investigated in the papers that analyzed genetic diversity using cpDNA markers: (a) Life mode; (b) Habitat specialization; (c) Geographic distribution; (d) Reproductive cycle; (e) Type of flower, and (f) Type of pollinator. Table S1. Plant species identified in the publications containing estimates of genetic diversity obtained from the use of cpDNA sequences as molecular markers. Group Family Species Algae Gigartinaceae Mazzaella laminarioides Angiospermae Typhaceae Typha laxmannii Angiospermae Typhaceae Typha orientalis Angiospermae Typhaceae Typha angustifolia Angiospermae Typhaceae Typha latifolia Angiospermae Araliaceae Eleutherococcus sessiliflowerus Angiospermae Polygonaceae Atraphaxis bracteata Angiospermae Plumbaginaceae Armeria pungens Angiospermae Aristolochiaceae Aristolochia kaempferi Angiospermae Polygonaceae Atraphaxis compacta Angiospermae Apocynaceae Lagochilus macrodontus Angiospermae Polygonaceae Atraphaxis -
Passiflora Tarminiana, a New Cultivated Species of Passiflora Subgenus
Novon 11(1): 8–15. 2001 Passiflora tarminiana, a new cultivated species of Passiflora subgenus Tacsonia. Geo Coppens d'Eeckenbrugge1, Victoria E. Barney1, Peter Møller Jørgensen2, John M. MacDougal2 1CIRAD-FLHOR/IPGRI Project for Neotropical Fruits, c/o CIAT, A.A. 6713, Cali Colombia 2Missouri Botanical Garden, P.O. Box 299, St Louis, Missouri 63166-0299, U.S.A. Abstract The new species Passiflora tarminiana differs from its closes relative by the character combination of very small acicular stipules and large almost reflexed petals and sepals. This species has escaped detection despite being widely cultivated. Naturalized populations, particularly on Hawa'ii, have created problems for conservation of the native flora. In Colombia it is more frequently adopted in industrial cultivation because of its rusticity and resistance to fungal diseases. Introduction Passifloras of the subgenus Tacsonia are cultivated by many small farmers, from Venezuela to Bolivia. Some species are cultivated in New Zealand. The main cultivated species is Passiflora mollissima (Kunth) Bailey (Escobar, 1980 & 1988), also called P. Coppens et al. 2000 Passiflora tarminiana 2 tripartita var. mollissima (Kunth) Holm-Nielsen & P. Jørgensen (Holm-Nielsen et al., 1988). It is called "curuba de Castilla" in Colombia, "tacso de Castilla" in Ecuador, and “banana passionfruit” in English-speaking countries.. The second species of importance in the Andes is "curuba india," "curuba ecuatoriana," or "curuba quiteña" in Colombia, called "tacso amarillo" in Ecuador (Pérez Arbeláez, 1978; A.A.A., 1992; Campos, 1992). It is most frequently found in private gardens, but some commercial growers have, because of its rusticity, started to grow it instead of the "curuba de Castilla." We describe this overlooked cultigen as a new species under the name Passiflora tarminiana, in recognition of Tarmín Campos, a Colombian agronomist who contributed with enthusiasm to the development of banana passion fruit cultivation and introduced the first author to the cultivated passifloras of the central Colombian highlands. -
RHS the Garden Magazine Index 2020
GardenThe INDEX 2020 Volume 145, Parts 1–12 Index 2020 January 2020 February 2020 March 2020 April 2020 May 2020 June 2020 1 2 3 4 5 6 Coloured numbers campestre ‘William ‘Voodoo’ 9: 78 ‘Kaleidoscope’ lauterbachiana Plas Brondanw, North in bold before the page Caldwell’ 3: 32, 32 ‘Zwartkop’ 7: 22, 22; 11: 46, 46 1: 56, 57 Wales 12: 38–42, 38–42 number(s) denote the x freemanii Autumn 8: 54, 54 ‘Lavender Lady’ 6: 12, macrorrhizos 11: 33, 33 Andrews, Susyn, on: part number (month). Blaze (‘Jeffersred’) Aeschynanthus 3: 138 12; 11: 46–47, 47 micholitziana 2: 78 hollies, AGM cultivars Each part is paginated 10: 14, 14–15 Aesculus ‘Macho Mocha’ Aloe Safari Sunrise (‘X5’) 12: 31, 31 separately. griseum 1: 49; 2: 14, 14– hippocastanum 11: 46, 47 6: 12, 12 Anemone: 15; 11: 34, 35; 12: 10, 10; ‘Hampton Court ‘Mayan Queen’ 11: 46 Aloysia: ‘Frilly Knickers’ 9: 7, 7 Numbers in italics 12: 83 Gold’ 3: 89, 89 ‘Pineapple Express’ citrodora (lemon Wild Swan denote an image. micrantham 10: 80 ‘Wisselink’ 3: 89, 89 11: 47 verbena) 6: 87, 87, 88; (‘Macane001’) 5: 74, palmatum 4: 74–75; x neglecta ‘Silver Fox’ 11: 47 to infuse gin 4: 82, 83 74, 76 Where a plant has a 12: 65, 65 ‘Erythroblastos’ Aglaonema (Chinese gratissima angelica root to infuse Trade Designation ‘Garnet’ 10: 27, 27 3: 88, 88 evergreen): 1: 57; 7: 34, (whitebrush or gin 4: 82, 82 (also known as a selling platanoides Agapanthus: 5: 82, 83 34; 12: 32, 32 spearmint verbena) Angelonia Serena Series name) it is typeset in ‘Walderseei’ 3: 87, 87 ‘Blue Dot 9: 109 ‘King of Siam’ 1: 56, 57 6: 86, 88 8: 16, 17 a different font to pseudoplatanus ‘Bressingham Blue’ pictum ‘Tricolor’ Alstroemeria: angel’s trumpet (see distinguish it from the ‘Brilliantissimum’ 9: 109 1: 44, 45 Indian Summer Brugmansia) cultivar name (shown 3: 86, 86–87 ‘Cally Blue 9: 109 Agrostis nebulosa (‘Tesronto’) 8: 16, 16 Angwin, Kirsty, on: in ‘Single Quotes’). -
H. Kiyosumiensis F
Hosta Species Update●The Hosta Library © W. George Schmid 2006 H. kiyosumiensis F. Maekawa 1935 Jornal of Japanese Botany 11:689; ic. f. 15 1935 キヨスミギボウシ = Kyosumi Giboshi H. kiyosumiensis var. petrophila F. Maekawa 1938 Divisiones et Plantae Novae Generis Hostae (2). J. Japanese Botany, 14:1:45–49. イワマ ギボウシ = Iwama Giboshi History and Nomenclature: In Japan this species is called Kyiosumi Giboshi, the “Kiyosumi (Mountain) Hosta.” The species epithet stems from the Latinized name of Kiyosumiyama (清澄山), a small mountain (380 m/about 1250 feet AMSL with a great view of Tokyo Bay) located on Boso Peninsula (Bōsō-hantō; 房総半島), which is located in south Chiba Prefecture (Chiba-ken; 千葉県) forming the eastern edge of Tokyo Bay. Maekawa established H. kiyosumiensis in 1935 and published further on the species in 1938, when he also described a new variety of the species as H. (kiyosumiensis var.) petrophila. This varietal epithet is derived from the Latin “liking (or) growing on rocks.” The Japanese name Iwama Giboshi (イワマ ギボウシ) has the same meaning. The latter is differentiated by minor morphological details caused by its different, rocky habitat in Yamashiro province (山城国; Yamashiro-no kuni), H. kiyosumiensis Maekawa 1935 (in situ) Otogawa (男川) River; Okazaki-shi (岡崎市; formerly Nukata-cho) Aichi Prefecture (愛知県; Aichi-ken) 1 an old province of Japan (today the southern part of Kyoto Prefecture). Maekawa (1938) gave a much abbreviated Latin description and the variety is here considered synonymous with the species. In fact, Maekawa (1969) no longer supported the varietal rank. N. Fujita (1976) confirmed H. kiyosumiensis as a species and added two morphs previously described by Maekawa (1940), i.e., H. -
Introduction Methods Results
Papers and Proceedings Royal Society ofTasmania, Volume 1999 103 THE CHARACTERISTICS AND MANAGEMENT PROBLEMS OF THE VEGETATION AND FLORA OF THE HUNTINGFIELD AREA, SOUTHERN TASMANIA by J.B. Kirkpatrick (with two tables, four text-figures and one appendix) KIRKPATRICK, J.B., 1999 (31:x): The characteristics and management problems of the vegetation and flora of the Huntingfield area, southern Tasmania. Pap. Proc. R. Soc. Tasm. 133(1): 103-113. ISSN 0080-4703. School of Geography and Environmental Studies, University ofTasmania, GPO Box 252-78, Hobart, Tasmania, Australia 7001. The Huntingfield area has a varied vegetation, including substantial areas ofEucalyptus amygdalina heathy woodland, heath, buttongrass moorland and E. amygdalina shrubbyforest, with smaller areas ofwetland, grassland and E. ovata shrubbyforest. Six floristic communities are described for the area. Two hundred and one native vascular plant taxa, 26 moss species and ten liverworts are known from the area, which is particularly rich in orchids, two ofwhich are rare in Tasmania. Four other plant species are known to be rare and/or unreserved inTasmania. Sixty-four exotic plantspecies have been observed in the area, most ofwhich do not threaten the native biodiversity. However, a group offire-adapted shrubs are potentially serious invaders. Management problems in the area include the maintenance ofopen areas, weed invasion, pathogen invasion, introduced animals, fire, mechanised recreation, drainage from houses and roads, rubbish dumping and the gathering offirewood, sand and plants. Key Words: flora, forest, heath, Huntingfield, management, Tasmania, vegetation, wetland, woodland. INTRODUCTION species with the most cover in the shrub stratum (dominant species) was noted. If another species had more than half The Huntingfield Estate, approximately 400 ha of forest, the cover ofthe dominant one it was noted as a codominant. -
Novel Habitats, Rare Plants and Root Traits
Lincoln University Digital Thesis Copyright Statement The digital copy of this thesis is protected by the Copyright Act 1994 (New Zealand). This thesis may be consulted by you, provided you comply with the provisions of the Act and the following conditions of use: you will use the copy only for the purposes of research or private study you will recognise the author's right to be identified as the author of the thesis and due acknowledgement will be made to the author where appropriate you will obtain the author's permission before publishing any material from the thesis. Novel Habitats, Rare Plants and Roots Traits A thesis submitted in partial fulfilment of the requirements for the Degree of Master of Applied Science at Lincoln University by Paula Ann Greer Lincoln University 2017 Abstract of a thesis submitted in partial fulfilment of the requirements for the Degree of Master of Applied Science. Abstract Novel habitats, rare plants and root traits. by Paula Ann Greer The loss of native plant species through habitat loss has been happening in NZ since the arrival of humans. This is especially true in Canterbury where less than 1% of the lowland plains are believed to be covered in remnant native vegetation. Rural land uses are changing and farm intensification is creating novel habitats, including farm irrigation earth dams. Dam engineers prefer not to have plants growing on dams. Earth dams are consented for 100 years, they could be used to support threatened native plants. Within the farm conversion of the present study dams have created an average of 1.7 hectares of ‘new land’ on their outside slope alone, which is the area of my research.