Native Plant Species in Te Urewera National Park
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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. -
1 Retail Listings 2011 by USDA Zone, As of Sept 5 - Please Check for Current Availability
1 Retail listings 2011 by USDA zone, as of Sept 5 - please check for current availability USDA zone: 2 Alcea rosea 'Nigra' Classic hollyhock with dark maroon, nearly black flowers covering the 5-8 ft spires in July and August. They like well-drained soil and full to part sun with average summer water. Short-lived, they reseed easily establishing long-lived colonies. Frost hardy in USDA zone 2. 4in @ $3 Malvaceae Lindelofia longiflora Bright blue flowered cousin of a forget-me-not which blooms from late spring to frost. Long-live perennial, clumping to 2 ft by 2 ft in rich, moist soil in a half shady spot– think woodland. Great for a border that gets some water, but not much attention otherwise. Hardy to 25 below. 6in @ $12 Boraginaceae Physocarpus opulifolius 'Dart's Gold' golden ninebark Its golden foliage highlights the pure white, fragrant, summer flowers and brilliant red fruit in autumn. Peeling bark adds interest to this durable hedging plant or specimen, deciduous, to 5 ft tall and wide, smaller than the species. Out of the hottest afternoon sun seems to suit it best for foliage color. Can take a bit of drought, but best with a little summer water. Takes will to pruning. Frost hardy in USDA zone 2. 1g @ $12, 2g @ $22 Rosaceae Rosa glauca red leaf rose Grown as much for its foliage as its flowers this deciduous shrub, to 6 ft tall x 5 ft wide, has glaucous blue foliage and, in June, single pink flowers with white centers. Lovely rose hips follow and remain through the winter. -
Otanewainuku ED (Report Prepared on 13 August 2013)
1 NZFRI collection wish list for Otanewainuku ED (Report prepared on 13 August 2013) Fern Ally Isolepis cernua Lycopodiaceae Isolepis inundata Lycopodium fastigiatum Isolepis marginata Lycopodium scariosum Isolepis pottsii Psilotaceae Isolepis prolifera Tmesipteris lanceolata Lepidosperma australe Lepidosperma laterale Gymnosperm Schoenoplectus pungens Cupressaceae Schoenoplectus tabernaemontani Chamaecyparis lawsoniana Schoenus apogon Cupressus macrocarpa Schoenus tendo Pinaceae Uncinia filiformis Pinus contorta Uncinia gracilenta Pinus patula Uncinia rupestris Pinus pinaster Uncinia scabra Pinus ponderosa Hemerocallidaceae Pinus radiata Dianella nigra Pinus strobus Phormium cookianum subsp. hookeri Podocarpaceae Phormium tenax Podocarpus totara var. totara Iridaceae Prumnopitys taxifolia Crocosmia xcrocosmiiflora Libertia grandiflora Monocotyledon Libertia ixioides Agapanthaceae Watsonia bulbillifera Agapanthus praecox Juncaceae Alliaceae Juncus articulatus Allium triquetrum Juncus australis Araceae Juncus conglomeratus Alocasia brisbanensis Juncus distegus Arum italicum Juncus edgariae Lemna minor Juncus effusus var. effusus Zantedeschia aethiopica Juncus sarophorus Arecaceae Juncus tenuis var. tenuis Rhopalostylis sapida Luzula congesta Asparagaceae Luzula multiflora Asparagus aethiopicus Luzula picta var. limosa Asparagus asparagoides Orchidaceae Cordyline australis x banksii Acianthus sinclairii Cordyline banksii x pumilio Aporostylis bifolia Asteliaceae Corunastylis nuda Collospermum microspermum Diplodium alobulum Commelinaceae -
Visit to Adelaide Botanic Garden Adelaide, South Australia 23-24
Visit to Adelaide Botanic Garden Adelaide, South Australia 23-24 th September 2006 Laura Fagan, Brad Howlett, Corina Till, Melanie Walker (Crop & Food Research) Background A visit was made to Adelaide Botanic Garden as part of the B3 IO3.5 Expatriate Plant Communities project. John Sandham, Collections Development Officer (see site visit report 28 Sept 06_Barratt) organised a garden duty officer, Enzo Vidoni, to guide the visit by Laura Fagan. Figure 1. Main entrance to Adelaide Botanic Figure 2. Wollemia Garden off Botanic Road. nobilis The Adelaide Botanic Garden is an historic garden on the Adelaide Plains with a dry Mediterranean climate and alkaline soils. The original 16 hectare (41 acre) garden was first opened to the public in 1857. Acquired by the Adelaide Botanic Garden in 1866, the adjacent Botanic Park is a glorious 34 hectare green oasis within easy walking distance of the Adelaide CBD. It is flanked on the Botanic Garden side by a stately avenue of Plane trees which were planted in 1874, and on the northern side by the River Torrens and the Adelaide Zoo. Century old Moreton Bay Fig trees from Queensland with their huge trunks and gnarled buttress roots add to the special quality of Botanic Park. The garden contains the oldest Australian forest tree species in the country including a single specimen of Wollemia nobilis and the largest Plain tree. Native and exotic plant collections are displayed including palms, cycads, bromeliads and many spectacular mature trees and shrubs. Rainforest species are grown in the temperate Australian forest and the Bicentennial Conservatory for tropical plants. -
Plant Charts for Native to the West Booklet
26 Pohutukawa • Oi exposed coastal ecosystem KEY ♥ Nurse plant ■ Main component ✤ rare ✖ toxic to toddlers coastal sites For restoration, in this habitat: ••• plant liberally •• plant generally • plant sparingly Recommended planting sites Back Boggy Escarp- Sharp Steep Valley Broad Gentle Alluvial Dunes Area ment Ridge Slope Bottom Ridge Slope Flat/Tce Medium trees Beilschmiedia tarairi taraire ✤ ■ •• Corynocarpus laevigatus karaka ✖■ •••• Kunzea ericoides kanuka ♥■ •• ••• ••• ••• ••• ••• ••• Metrosideros excelsa pohutukawa ♥■ ••••• • •• •• Small trees, large shrubs Coprosma lucida shining karamu ♥ ■ •• ••• ••• •• •• Coprosma macrocarpa coastal karamu ♥ ■ •• •• •• •••• Coprosma robusta karamu ♥ ■ •••••• Cordyline australis ti kouka, cabbage tree ♥ ■ • •• •• • •• •••• Dodonaea viscosa akeake ■ •••• Entelea arborescens whau ♥ ■ ••••• Geniostoma rupestre hangehange ♥■ •• • •• •• •• •• •• Leptospermum scoparium manuka ♥■ •• •• • ••• ••• ••• ••• ••• ••• Leucopogon fasciculatus mingimingi • •• ••• ••• • •• •• • Macropiper excelsum kawakawa ♥■ •••• •••• ••• Melicope ternata wharangi ■ •••••• Melicytus ramiflorus mahoe • ••• •• • •• ••• Myoporum laetum ngaio ✖ ■ •••••• Olearia furfuracea akepiro • ••• ••• •• •• Pittosporum crassifolium karo ■ •• •••• ••• Pittosporum ellipticum •• •• Pseudopanax lessonii houpara ■ ecosystem one •••••• Rhopalostylis sapida nikau ■ • •• • •• Sophora fulvida west coast kowhai ✖■ •• •• Shrubs and flax-like plants Coprosma crassifolia stiff-stemmed coprosma ♥■ •• ••••• Coprosma repens taupata ♥ ■ •• •••• •• -
I UNIVERSIDADE ESTADUAL DE CAMPINAS INSTITUTO DE
UNIVERSIDADE ESTADUAL DE CAMPINAS INSTITUTO DE BIOLOGIA DEPARTAMENTO DE BOTÂNICA ANDRÉA MACÊDO CORRÊA CITOTAXONOMIA DE REPRESENTANTES DA SUBFAMÍLIA RUBIOIDEAE (RUBIACEAE) NOS CERRADOS DO ESTADO DE SÃO PAULO Tese apresentada ao Instituto de Biologia para obtenção do Título de Doutor em Biologia Vegetal Orientadora: Profª. Drª. Eliana Regina Forni-Martins Campinas 2007 i ii Campinas, 02 de Março de 2007 BANCA EXAMINADORA Drª. Eliana Regina Forni-Martins – Orientadora Drª. Maria Angélica Maciel Martinho Ferreira Drª. Sigrid Luiza Jung Mendaçolli Drª. Neiva Isabel Pierozzi Dr. João Semir Drª. Luiza Sumiko Kinoshita - Suplente ______________________________________ Dr. Ricardo Lombelo - Suplente ______________________________________ Drª. Júlia Yamagishi Costa - Suplente ______________________________________ iii À minha família, de valor inestimável. iv AGRADECIMENTOS Este trabalho foi concluído graças ao apoio e dedicação de várias pessoas, que contribuíram direta ou indiretamente para sua realização. Agradeço então: A Deus; À minha família, Agostinho e Aracilda, meus pais, Araceli e Junior, meus irmãos, Otávio Augusto, meu sobrinho, pelo apoio, mesmo à distância; Ao meu marido Emerson, pelo apoio, companheirismo e auxílio nas coletas no campo; À Drª. Eliana, minha orientadora, que novamente confiou no meu trabalho, ensinando e ajudando em diversos momentos; À Universidade Estadual de Campinas, Instituto de Biologia, Departamento de Botânica, Laboratório de Biossistemática, pela infra-estrutura que possibilitou a realização desse trabalho; Ao curso de Pós-graduação em Biologia Vegetal; À FAPESP (Fundação de Apoio à Pesquisa do Estado de São Paulo), pela bolsa de doutorado concedida e os auxílios fornecidos a Drª. Eliana, possibilitando a realização dessa pesquisa; Ao CNPq (Conselho Nacional de Pesquisa e Desenvolvimento Tecnológico) pelo auxílio concedido a Drª. -
Hidden in Plain Sight—A New Species of Lichen Strigula Oleistrata March 2020 (Strigulaceae) from New Zealand
TRILEPIDEA Newsletter of the New Zealand Plant Conservation Network NO. 196 Hidden in Plain sight—a new species of lichen Strigula oleistrata March 2020 (Strigulaceae) from New Zealand. Deadline for next issue: Marley Ford ([email protected]); Dan J. Blanchon ([email protected]), Friday 19 April 2020 School of Environmental & Animal Sciences, Unitec Institute of Technology, Auckland; SUBMIT AN ARTICLE Peter J. de Lange ([email protected]), School of Environmental & Animal TO THE NEWSLETTER Sciences, Unitec Institute of Technology, Auckland Contributions are welcome New Zealand has a surprising diversity of Strigula. 25 species of the genus are found to the newsletter at any here out of the c.70 species recognised; representing over a third of the known species time. The closing date for articles for each issue is (Galloway 2007, Lücking 2008, Hyde et al. 2013). Most of these species are foliicolous, approximately the 15th of meaning that they live on the surfaces of leaves. However, a few species do colonise each month. rocks and bark (Galloway 2007). Articles may be edited and used in the newsletter and/ Between 2016 and 2017 the senior author undertook a third year, level 7 School of or on the website news page. Environmental & Animal Sciences self-directed paper studying Strigula novae- The Network will publish zelandiae at the Unitec Institute of Technology Herbarium (UNITEC). Strigula novae- almost any article about zelandiae is a foliicolous species that is sometimes known as ‘silver paint lichen’, because plants and plant conservation with a particular focus on the when dead the thallus imparts a silvery patterning on the leaves it has colonised. -
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TRILEPIDEA Newsletter of the New Zealand Plant Conservation Network NO. 185 CONFERENCE REGISTRATION OPEN NOW! May 2019 We invite you to register for the 2019 Australasian Systematic Botany Society and New Deadline for next issue: Zealand Plant Conservation Network joint conference to be held at the Museum of New Monday 20 May 2019 Zealand Te Papa Tongarewa, Wellington, New Zealand in the last week of November. SUBMIT AN ARTICLE Start planning now! Spaces in workshops and fi eld trips are limited, so register early to TO THE NEWSLETTER get your top choices. Contributions are welcome Check out the recently updated conference website to get all the important details to the newsletter at any time. The closing date for about conference dates, venue, accommodation, programme, keynote speakers, fi eld articles for each issue is trips, workshops, silent auction, and more! approximately the 15th of each month. The conference theme, ‘Taxonomy for Plant Conservation – Ruia mai i Rangiātea’ aims to capitalise on the vast expertise of our two societies. There will be multiple upskilling Articles may be edited and used in the newsletter and/ workshops, three days of symposia, and a chance to explore Wellington’s forests and or on the website news page. rugged coastlines on our fi ve diff erent full-day fi eld trips. The Network will publish Feel free to contact the organising committee by email if you have any queries: almost any article about [email protected], otherwise go to the conference website (https://systematics. plants and plant conservation with a particular focus on the ourplants.org/) to keep up to date with developments, or follow us on Facebook or plant life of New Zealand and Twitter for announcements. -
Lankesteriana IV
LANKESTERIANA 7(1-2): 229-239. 2007. DENSITY INDUCED RATES OF POLLINARIA REMOVAL AND DEPOSITION IN THE PURPLE ENAMEL-ORCHID, ELYTHRANTHERA BRUNONIS (ENDL.) A.S. GEORGE 1,10 2 3 RAYMOND L. TREMBLAY , RICHARD M. BATEMAN , ANDREW P. B ROWN , 4 5 6 7 MARC HACHADOURIAN , MICHAEL J. HUTCHINGS , SHELAGH KELL , HAROLD KOOPOWITZ , 8 9 CARLOS LEHNEBACH & DENNIS WIGHAM 1 Department of Biology, 100 Carr. 908, University of Puerto Rico – Humacao campus, Humacao, Puerto Rico, 00791-4300, USA 2 Natural History Museum, Cromwell Road, London SW7 5BD, UK 3 Department of Environment and Conservation, Species and Communities Branch, Locked Bag 104 Bentley Delivery Centre WA 6893, Australia 4 New York Botanic Garden, 112 Alpine Terrace, Hilldale, NJ 00642, USA 5 School of Life Sciences, University of Sussex, Falmer, Brighton, Sussex, BN1 9QG, UK 6 IUCN/SSC Orchid Specialist Group Secretariat, 36 Broad Street, Lyme Regis, Dorset, DT7 3QF, UK 7 University of California, Ecology and Evolutionary Biology, Irvine, CA 92697, USA 8 Massey University, Allan Wilson Center for Molecular Ecology and Evolution 9 Smithsonian Institution, Smithsonian Environmental Research Center, Box 28, Edgewater, MD 21037, USA 10 Author for correspondence: [email protected] RESUMEN. La distribución y densidad de los individuos dentro de las poblaciones de plantas pueden afectar el éxito reproductivo de sus integrantes. Luego de describir la filogenia de las orquideas del grupo de las Caladeniideas y su biología reproductiva, evaluamos el efecto de la densidad en el éxito reproductivo de la orquídea terrestre Elythranthera brunonis, endémica de Australia del Oeste. El éxito reproductivo de esta orquídea, medido como la deposición y remoción de polinios, fue evaluado. -
INDEX for 2011 HERBALPEDIA Abelmoschus Moschatus—Ambrette Seed Abies Alba—Fir, Silver Abies Balsamea—Fir, Balsam Abies
INDEX FOR 2011 HERBALPEDIA Acer palmatum—Maple, Japanese Acer pensylvanicum- Moosewood Acer rubrum—Maple, Red Abelmoschus moschatus—Ambrette seed Acer saccharinum—Maple, Silver Abies alba—Fir, Silver Acer spicatum—Maple, Mountain Abies balsamea—Fir, Balsam Acer tataricum—Maple, Tatarian Abies cephalonica—Fir, Greek Achillea ageratum—Yarrow, Sweet Abies fraseri—Fir, Fraser Achillea coarctata—Yarrow, Yellow Abies magnifica—Fir, California Red Achillea millefolium--Yarrow Abies mariana – Spruce, Black Achillea erba-rotta moschata—Yarrow, Musk Abies religiosa—Fir, Sacred Achillea moschata—Yarrow, Musk Abies sachalinensis—Fir, Japanese Achillea ptarmica - Sneezewort Abies spectabilis—Fir, Himalayan Achyranthes aspera—Devil’s Horsewhip Abronia fragrans – Sand Verbena Achyranthes bidentata-- Huai Niu Xi Abronia latifolia –Sand Verbena, Yellow Achyrocline satureoides--Macela Abrus precatorius--Jequirity Acinos alpinus – Calamint, Mountain Abutilon indicum----Mallow, Indian Acinos arvensis – Basil Thyme Abutilon trisulcatum- Mallow, Anglestem Aconitum carmichaeli—Monkshood, Azure Indian Aconitum delphinifolium—Monkshood, Acacia aneura--Mulga Larkspur Leaf Acacia arabica—Acacia Bark Aconitum falconeri—Aconite, Indian Acacia armata –Kangaroo Thorn Aconitum heterophyllum—Indian Atees Acacia catechu—Black Catechu Aconitum napellus—Aconite Acacia caven –Roman Cassie Aconitum uncinatum - Monkshood Acacia cornigera--Cockspur Aconitum vulparia - Wolfsbane Acacia dealbata--Mimosa Acorus americanus--Calamus Acacia decurrens—Acacia Bark Acorus calamus--Calamus -
Orchid Historical Biogeography, Diversification, Antarctica and The
Journal of Biogeography (J. Biogeogr.) (2016) ORIGINAL Orchid historical biogeography, ARTICLE diversification, Antarctica and the paradox of orchid dispersal Thomas J. Givnish1*, Daniel Spalink1, Mercedes Ames1, Stephanie P. Lyon1, Steven J. Hunter1, Alejandro Zuluaga1,2, Alfonso Doucette1, Giovanny Giraldo Caro1, James McDaniel1, Mark A. Clements3, Mary T. K. Arroyo4, Lorena Endara5, Ricardo Kriebel1, Norris H. Williams5 and Kenneth M. Cameron1 1Department of Botany, University of ABSTRACT Wisconsin-Madison, Madison, WI 53706, Aim Orchidaceae is the most species-rich angiosperm family and has one of USA, 2Departamento de Biologıa, the broadest distributions. Until now, the lack of a well-resolved phylogeny has Universidad del Valle, Cali, Colombia, 3Centre for Australian National Biodiversity prevented analyses of orchid historical biogeography. In this study, we use such Research, Canberra, ACT 2601, Australia, a phylogeny to estimate the geographical spread of orchids, evaluate the impor- 4Institute of Ecology and Biodiversity, tance of different regions in their diversification and assess the role of long-dis- Facultad de Ciencias, Universidad de Chile, tance dispersal (LDD) in generating orchid diversity. 5 Santiago, Chile, Department of Biology, Location Global. University of Florida, Gainesville, FL 32611, USA Methods Analyses use a phylogeny including species representing all five orchid subfamilies and almost all tribes and subtribes, calibrated against 17 angiosperm fossils. We estimated historical biogeography and assessed the -
Indigenous Plant Naming and Experimentation Reveal a Plant–Insect Relationship in New Zealand Forests
Received: 23 February 2020 Revised: 10 August 2020 Accepted: 25 August 2020 DOI: 10.1111/csp2.282 CONTRIBUTED PAPER Indigenous plant naming and experimentation reveal a plant–insect relationship in New Zealand forests Priscilla M. Wehi1,2 | Gretchen Brownstein2 | Mary Morgan-Richards1 1School of Agriculture and Environment, Massey University, Palmerston North, Abstract New Zealand Drawing from both Indigenous and “Western” scientific knowledge offers the 2Manaaki Whenua Landcare Research, opportunity to better incorporate ecological systems knowledge into conserva- Dunedin, New Zealand tion science. Here, we demonstrate a “two-eyed” approach that weaves Indige- Correspondence nous ecological knowledge (IK) with experimental data to provide detailed and Priscilla M. Wehi, Manaaki Whenua comprehensive information about regional plant–insect interactions in Landcare Research, 764 Cumberland New Zealand forests. We first examined Maori names for a common forest Street, Dunedin 9053, New Zealand. Email: [email protected], tree, Carpodetus serratus, that suggest a close species interaction between an [email protected] herbivorous, hole-dwelling insect, and host trees. We detected consistent – Funding information regional variation in both Maori names for C. serratus and the plant insect Foundation for Research, Science and relationship that reflect Hemideina spp. abundances, mediated by the presence Technology; Royal Society of New Zealand of a wood-boring moth species. We found that in regions with moths C. serratus trees are home to more weta than adjacent forest species and that these weta readily ate C. serratus leaves, fruits and seeds. These findings con- firm that a joint IK—experimental approach can stimulate new hypotheses and reveal spatially important ecological patterns.