Washington Geology, V, 22, No. 3, September 1994
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A New Species from Southern Namibia ⁎ W
Available online at www.sciencedirect.com South African Journal of Botany 77 (2011) 608–612 www.elsevier.com/locate/sajb Commiphora buruxa (Burseraceae), a new species from southern Namibia ⁎ W. Swanepoel H.G.W.J. Schweickerdt Herbarium, Department of Plant Science, University of Pretoria, Pretoria 0002, South Africa Received 16 August 2010; received in revised form 23 November 2010; accepted 7 December 2010 Abstract Commiphora buruxa Swanepoel, described here as a new species, is known only from the Gariep Centre of Endemism, southwestern Namibia. It appears to be most closely related to C. cervifolia Van der Walt. Diagnostic morphological characters of C. buruxa include a viscous, cream-coloured exudate, variably simple to trifoliolate leaves, and a putamen covered by a small cupular pseudo-aril. Illustrations of the plant and a distribution map are provided. The species is known from less than 20 plants. © 2011 SAAB. Published by Elsevier B.V. All rights reserved. Keywords: Burseraceae; Commiphora; Gariep Centre; New species; Southern Africa; Taxonomy 1. Introduction molecular evidence subsequently confirmed that they represent an undescribed species of Commiphora. In November 2006, At present thirty-eight described species of Commiphora during a botanical expedition to the Huns Mountains about Jacq. are known from the Flora of southern Africa region, no 100 km further to the north–northwest, another population of less than thirty of which occur in Namibia (Craven, 1999; the same species was found on the lower slopes of these Germishuizen and Meyer, 2003; Swanepoel, 2005, 2006, 2007, mountains, growing in a valley leading to the Konkiep River. 2008). Five of these species are endemic or near-endemic to the Apparently no other collections of the new species exist, as no Gariep Centre of Endemism, a biogeographical region along the herbarium specimens could be found in either PRE or WIND. -
Amelanchierspp. Family: Rosaceae Serviceberry
Amelanchier spp. Family: Rosaceae Serviceberry The genus Amelanchier contains about 16 species native to North America [5], Mexico [2], and Eurasia to northern Africa [4]. The word amelanchier is derived from the French common name amelanche of the European serviceberry, Amelanchier ovalis. Amelanchier alnifolia-juneberry, Pacific serviceberry, pigeonberry, rocky mountain servicetree, sarvice, sarviceberry, saskatoon, saskatoon serviceberry, western service, western serviceberry , western shadbush Amelanchier arborea-Allegheny serviceberry, apple shadbush, downy serviceberry , northern smooth shadbush, shadblow, shadblown serviceberry, shadbush, shadbush serviceberry Amelanchier bartramiana-Bartram serviceberry Amelanchier canadensis-American lancewood, currant-tree, downy serviceberry, Indian cherry, Indian pear, Indian wild pear, juice plum, juneberry, may cherry, sugar plum, sarvice, servicetree, shadberry, shadblow, shadbush, shadbush serviceberry, shadflower, thicket serviceberry Amelanchier florida-Pacific serviceberry Amelanchier interior-inland serviceberry Amelanchier sanguinea-Huron serviceberry, roundleaf juneberry, roundleaf serviceberry , shore shadbush Amelanchier utahensis-Utah serviceberry Distribution In North America throughout upper elevations and temperate forests. The Tree Serviceberry is a shrub or tree that reaches a height of 40 ft (12 m) and a diameter of 2 ft (0.6 m). It grows in many soil types and occurs from swamps to mountainous hillsides. It flowers in early spring, producing delicate white flowers, making -
Cephalotaxus
Reprinted from the Winter 1970 issue of t'he THE AMERICA HORTICULTURAL \t{AGAZIl\'E Copyright 1970 by The American Horticultural Society, Inc. Cephalotaxus Source of Harringtonine, A Promising New Anti..Cancer Alkaloid ROBERT E. PERDUE, JR.,l LLOYD A. SPETZMAN,l and RICHARD G. POWELL2 The plumyews (Cephalotaxus) are yew-like evergreen trees and shrubs. The genus includes seven species native to southeastern Asia from Japan and Korea to Taiwan and Hainan, and west through China to northeastern India. Two species are in cultivation in the United States, C. harringtoniaJ (Fig. 1 & 2) of which there are several varieties (one often listed as C. drupacea) , and C. fortunii (Fig. 3). The cultivars are shrubs up to about 20 feet in height; most have broad crowns. The linear and pointed leaves are spirally arranged or in two opposite ranks. The upper sur Fig. 1. Japanese plumyew (Cephalo face is dark shiny green with a conspicu taxus harringtonia var. drupacea), an ous mid-rib; the lower surface has a evergreen shrub about 6 ft. high, at broad silvery band on either side of the the USDA Plant Introduction Station, mid-rib. These bands are made up of Glenn Dale, Maryland. This photo conspicuous white stomata arranged in graph was made in 1955. The plant is numerous distinct lines. Leaf length is now about 7 ft. high, but the lower variable, from about one inch in varie branches have been severely pruned ties of C. harringtonia to three or four to provide material for chemical re inches in C. fortunii. The leaves are search. -
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 -
Outline of Angiosperm Phylogeny
Outline of angiosperm phylogeny: orders, families, and representative genera with emphasis on Oregon native plants Priscilla Spears December 2013 The following listing gives an introduction to the phylogenetic classification of the flowering plants that has emerged in recent decades, and which is based on nucleic acid sequences as well as morphological and developmental data. This listing emphasizes temperate families of the Northern Hemisphere and is meant as an overview with examples of Oregon native plants. It includes many exotic genera that are grown in Oregon as ornamentals plus other plants of interest worldwide. The genera that are Oregon natives are printed in a blue font. Genera that are exotics are shown in black, however genera in blue may also contain non-native species. Names separated by a slash are alternatives or else the nomenclature is in flux. When several genera have the same common name, the names are separated by commas. The order of the family names is from the linear listing of families in the APG III report. For further information, see the references on the last page. Basal Angiosperms (ANITA grade) Amborellales Amborellaceae, sole family, the earliest branch of flowering plants, a shrub native to New Caledonia – Amborella Nymphaeales Hydatellaceae – aquatics from Australasia, previously classified as a grass Cabombaceae (water shield – Brasenia, fanwort – Cabomba) Nymphaeaceae (water lilies – Nymphaea; pond lilies – Nuphar) Austrobaileyales Schisandraceae (wild sarsaparilla, star vine – Schisandra; Japanese -
Section 2. Jack Pine (Pinus Banksiana)
SECTION 2. JACK PINE - 57 Section 2. Jack pine (Pinus banksiana) 1. Taxonomy and use 1.1. Taxonomy The largest genus in the family Pinaceae, Pinus L., which consists of about 110 pine species, occurs naturally through much of the Northern Hemisphere, from the far north to the cooler montane tropics (Peterson, 1980; Richardson, 1998). Two subgenera are usually recognised: hard pines (generally with much resin, wood close-grained, sheath of a leaf fascicle persistent, two fibrovascular bundles per needle — the diploxylon pines); and soft, or white pines (generally little resin, wood coarse-grained, sheath sheds early, one fibrovascular bundle in a needle — the haploxylon pines). These subgenera are called respectively subg. Pinus and subg. Strobus (Little and Critchfield, 1969; Price et al., 1998). Occasionally, one to about half the species (20 spp.) in subg. Strobus are classified instead in a variable subg. Ducampopinus. Jack pine (Pinus banksiana Lamb.) and its close relative lodgepole pine (Pinus contorta Dougl. Ex Loud.) are in subg. Pinus, subsection Contortae, which is classified either in section Trifoliis or a larger section Pinus (Little and Critchfield, 1969; Price et al., 1998). Additionally, subsect. Contortae usually includes Virginia pine (P. virginiana) and sand pine (P. clausa), which are in southeastern USA. Jack pine has two quite short (2-5 cm) stiff needles per fascicle (cluster) and lopsided (asymmetric) cones that curve toward the branch tip, and the cone scales often have a tiny prickle at each tip (Kral, 1993). Non-taxonomic ecological or biological variants of jack pine have been described, including dwarf, pendulous, and prostrate forms, having variegated needle colouration, and with unusual branching habits (Rudolph and Yeatman, 1982). -
Torreya Taxifolia
photograph © Abraham Rammeloo Torreya taxifolia produces seeds in 40 Kalmthout Arboretum ABRAHAM RAMMELOO, Curator of the Kalmthout Arboretum, writes about this rare conifer that recently produced seed for the first time. Torreya is a genus of conifers that comprises four to six species that are native to North America and Asia. It is closely related to Taxus and Cephalotaxus and is easily confused with the latter. However, it is relatively easy to distinguish them apart by their leaves. Torreya has needles with, on the underside, two small edges with stomas giving it a green appearance; Cephalotaxus has different rows of stomas, and for this reason the underside is more of a white colour. It is very rare to find Torreya taxifolia in the wild; it is native to a small area in Florida and Georgia. It grows in steep limestone cliffs along the Apalachicola River. These trees come from a warm and humid climate where the temperature in winter occasionally falls below freezing. They grow mainly on north-facing slopes between Fagus grandifolia, Liriodendron tulipifera, Acer barbatum, Liquidambar styraciflua and Quercus alba. They can grow up to 15 to 20 m high. The needles are sharp and pointed and grow in a whorled pattern along the branches. They are 25 to 35 mm long and stay on the tree for three to four years. If you crush them, they give off a strong, sharp odour. The health and reproduction of the adult population of this species suffered INTERNATIONAL DENDROLOGY SOCIETY TREES Opposite Torreya taxifolia ‘Argentea’ growing at Kalmthout Arboretum in Belgium. -
Amelanchier Canadensis
AmelanchierAmelanchier canadensiscanadensis ShadblowShadblow serviceberry,serviceberry, CanadianCanadian serviceberry,serviceberry, DownyDowny serviceberry,serviceberry, Shadbush,Shadbush, Juneberry,Juneberry, ChuckleberryChuckleberry Amelanchier canadensis(Shadblow serviceberry) is native to South Canada and the eastern United States. The shrub was introduced in Europe in 1746. The Shadblow serviceberry grows up to 5 to 6 metres tall and wide with a finely branched, wide vase-shaped crown. Before the leaves start to sprout, the Amelanchier canadensisblooms bountifully racemes of white flowers that hang over slightly. In late July, it bears red-violet to blue-black fruits that are edible. The leaves are relatively large and bud in a lovely bronze-red. In the summer, the Shadblow serviceberry has green leaves with a grey-green underside. The autumn colours are yellow-orange to brown and less striking than those of other serviceberry shrubs. The species has a preference for sunlight and moist, humous, slightly acidic soil. It will tolerate a temporarily dry environment, as well as strong wind. That makes Amelanchier canadensis very suitable for use in containers and roof gardens. SEASONAL COLOURS jan feb mar apr mei jun jul aug sep okt nov dec TYPES OF PLANTING Tree types: fruit trees, solitary shrubs | Topiary on stem: multi-stem umbrella USE Location: park, central reservation, in containers, roof garden, large garden, small garden, patio, cemetery, countryside, ecological zone | Pavement: none, open | Planting concepts: Eco planting, -
Plant Collecting Expedition for Berry Crop Species Through Southeastern
Plant Collecting Expedition for Berry Crop Species through Southeastern and Midwestern United States June and July 2007 Glassy Mountain, South Carolina Participants: Kim E. Hummer, Research Leader, Curator, USDA ARS NCGR 33447 Peoria Road, Corvallis, Oregon 97333-2521 phone 541.738.4201 [email protected] Chad E. Finn, Research Geneticist, USDA ARS HCRL, 3420 NW Orchard Ave., Corvallis, Oregon 97330 phone 541.738.4037 [email protected] Michael Dossett Graduate Student, Oregon State University, Department of Horticulture, Corvallis, OR 97330 phone 541.738.4038 [email protected] Plant Collecting Expedition for Berry Crops through the Southeastern and Midwestern United States, June and July 2007 Table of Contents Table of Contents.................................................................................................................... 2 Acknowledgements:................................................................................................................ 3 Executive Summary................................................................................................................ 4 Part I – Southeastern United States ...................................................................................... 5 Summary.............................................................................................................................. 5 Travelog May-June 2007.................................................................................................... 6 Conclusions for part 1 ..................................................................................................... -
A Sibling Species of the Persian Parrotia
The Chinese Parrotia: A Sibling Species of the Persian Parrotia Jianhua Li and Peter Del Tredici he Persian ironwood (Parrotia persica) The Persian and Chinese ironwoods are has a well-deserved reputation as a beau- members of the witch hazel family (Hama- Ttiful garden plant—mainly because of its melidaceae), and in order to appreciate their exfoliating bark and gorgeous fall color—but uniqueness and evolutionary history we need also as a tough species that tolerates drought, to first examine one of their more familiar rela- heat, wind, and cold (Dirr 1998). Less well tives, the witch hazels (Hamamelis). There are known is the fact that Persian ironwood has five species of witch hazel distributed through- a sister species, the Chinese ironwood (Parro- out the temperate regions: H. mollis in eastern tia subaequalis) (Figure 1), growing about 5600 China, H. japonica in Japan, and H. virginiana, kilometers (3500 miles) away in eastern China. H. vernalis, H. mexicana in North America. Remarkably, this species was correctly identi- The genus shows the intercontinental disjunct fied only sixteen years ago (Deng et al. 1992a). distribution between eastern Asia and North Figure 1. Geographic distribution of Parrotia persica (in green) and P. subaequalis (in red). Note that the scale bar is 400 kilometers. Parrotia 3 Hamamelis virginiana ..... Distyliopsis tutcheri 55 84 Distylium racemosum UBC Botanical Garden Sycopsis sinensis ................... 100 ➙ MOBOT Parrotia persica ........... 91 7.8±3.8 mya Parrotia subaequalis ................................. 50 mya Parrotiopsis jacquemontana ......... Fothergilla major .... 10 changes Figure 2. Evolutionary relationships of Hamamelis and petalless genera, showing shift (the arrow) from insect to wind pollination. -
Post-Wildfire Response of Shasta Snow-Wreath
California Fish and Wildlife, Fire Special Issue; 92-98; 2020 RESEARCH NOTE Post-wildfire response of Shasta snow-wreath LEN LINDSTRAND III1*, JULIE A. KIERSTEAD2, AND DEAN W. TAYLOR3 † 1Sierra Pacific Industries,P .O. Box 496014, Redding, CA 96049-6014, USA 2P. O. Box 491536, Redding CA, 96049, USA 33212 Redwood Drive, Aptos, CA, 95003, USA † Deceased *Corresponding Author: [email protected] Key words: Hirz fire, Neviusia cliftonii, post-wildfire response, Shasta snow-wreath, vegetative reproduction __________________________________________________________________________ Shasta snow-wreath (Neviusia cliftonii) is a rare shrub of the Rosaceae: tribe Kerrieae endemic to the southeastern Klamath Mountains in the general vicinity of Shasta Lake, Shasta County, California. The species was discovered less than 30 years ago (Shevock et al. 1992; Taylor 1993) and initially considered a limestone obligate. Subsequent occurrences have also been found on various non-limestone substrates (Lindstrand and Nelson 2005a, b, 2006; DeWoody et al. 2012; Jules et al. 2017). The only congener, Alabama snow-wreath (Neviusia alabamensis), also has a limited range restricted to several disjunct populations in the southeastern United States and occurs on limestone and non-limestone sedimentary substrates (Long 1989; Freiley 1994). Shasta snow-wreath is deciduous and produces flowers with showy white stamens, five toothed green sepals, and rarely, one to three narrow white petals. Based on our observations since its discovery, the species reproduces vegetatively, forming thickets of stems from the root system. Despite observations of developing achenes, no viable seed nor seedlings have been collected or observed. We are not aware of any pollinators and the blooms lack detect- able scent. -
Medicinal Plant Conservation
MEDICINAL Medicinal Plant PLANT SPECIALIST GROUP Conservation Silphion Volume 11 Newsletter of the Medicinal Plant Specialist Group of the IUCN Species Survival Commission Chaired by Danna J. Leaman Chair’s note . 2 Sustainable sourcing of Arnica montana in the International Standard for Sustainable Wild Col- Apuseni Mountains (Romania): A field project lection of Medicinal and Aromatic Plants – Wolfgang Kathe . 27 (ISSC-MAP) – Danna Leaman . 4 Rhodiola rosea L., from wild collection to field production – Bertalan Galambosi . 31 Regional File Conservation data sheet Ginseng – Dagmar Iracambi Medicinal Plants Project in Minas Gerais Lange . 35 (Brazil) and the International Standard for Sus- tainable Wild Collection of Medicinal and Aro- Conferences and Meetings matic Plants (ISSC-MAP) – Eleanor Coming up – Natalie Hofbauer. 38 Gallia & Karen Franz . 6 CITES News – Uwe Schippmann . 38 Conservation aspects of Aconitum species in the Himalayas with special reference to Uttaran- Recent Events chal (India) – Niranjan Chandra Shah . 9 Conservation Assessment and Management Prior- Promoting the cultivation of medicinal plants in itisation (CAMP) for wild medicinal plants of Uttaranchal, India – Ghayur Alam & Petra North-East India – D.K. Ved, G.A. Kinhal, K. van de Kop . 15 Ravikumar, R. Vijaya Sankar & K. Haridasan . 40 Taxon File Notices of Publication . 45 Trade in East African Aloes – Sara Oldfield . 19 Towards a standardization of biological sustain- List of Members. 48 ability: Wildcrafting Rhatany (Krameria lap- pacea) in Peru – Maximilian