Plant List 2011
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Molecular Phylogenetic Analysis of Japanese Miscanthus (Poaceae)
ISSN 1346-7565 Acta Phytotax. Geobot. 68 (2): 83–92 (2017) doi: 10.18942/apg.201703 Molecular Phylogenetic Analysis of Japanese Miscanthus (Poaceae) 1 2 3,† 2 HIDENORI NAKAMORI , MIKI TOMITA , HIROSHI AZUMA , TAKEHIRO MASUZAWA 2,* AND TORU TOKUOKA 1Graduate School of Integrated Science and Technology, Shizuoka University, Ohya, Suruga-ku, Shizuoka, 422-8529, Japan; 2Department of Biological Science, Faculty of Science, Shizuoka University, Ohya, Suruga-ku, Shizuoka, 422-8529, Japan. *[email protected] (author for corresponding); 3Department of Botany, Graduate School of Science, Kyoto University, Kitashirakawa-oiwake-cho, Sakyo-ku, Kyoto 606-8502, Japan; †Present Name & address: HIROSHI SUZUKI; Liberal arts and Sciences, Faculty of Engineering, Toyama Prefectural University, 5180 Kurokawa, Imizu-shi, Toyama 939-0398, Japan Miscanthus (Poaceae) comprises about 20 species, of which seven species and two forms occur in Japan. There is controversy whether M. condensatus is a separate species or a variety or subspecies of M. sinen- sis. To determine its taxonomic status, we conducted a molecular phylogenetic analysis using DNA se- quences of the atpB-rbcL, psbC-trnS(UGA), rpl20-rps12, trnL(UAA)-trnF(GAA), trnS(GGA)- trnT(UGU), and nuclear ITS regions, and the Adh1 gene from 31 samples of the seven Japanese species of Miscanthus. The neighbor-joining (NJ) tree based on the cpDNA sequences shows that M. condensa- tus and M. sinensis share two haplotypes, and that the nuclear ITS and Adh1 sequences of the two species are identical, making it difficult to distinguishM. condensatus from M. sinensis based on DNA sequenc- es. The evidence indicates that hybridization between the two species has proceeded rapidly, or that M. -
State of New York City's Plants 2018
STATE OF NEW YORK CITY’S PLANTS 2018 Daniel Atha & Brian Boom © 2018 The New York Botanical Garden All rights reserved ISBN 978-0-89327-955-4 Center for Conservation Strategy The New York Botanical Garden 2900 Southern Boulevard Bronx, NY 10458 All photos NYBG staff Citation: Atha, D. and B. Boom. 2018. State of New York City’s Plants 2018. Center for Conservation Strategy. The New York Botanical Garden, Bronx, NY. 132 pp. STATE OF NEW YORK CITY’S PLANTS 2018 4 EXECUTIVE SUMMARY 6 INTRODUCTION 10 DOCUMENTING THE CITY’S PLANTS 10 The Flora of New York City 11 Rare Species 14 Focus on Specific Area 16 Botanical Spectacle: Summer Snow 18 CITIZEN SCIENCE 20 THREATS TO THE CITY’S PLANTS 24 NEW YORK STATE PROHIBITED AND REGULATED INVASIVE SPECIES FOUND IN NEW YORK CITY 26 LOOKING AHEAD 27 CONTRIBUTORS AND ACKNOWLEGMENTS 30 LITERATURE CITED 31 APPENDIX Checklist of the Spontaneous Vascular Plants of New York City 32 Ferns and Fern Allies 35 Gymnosperms 36 Nymphaeales and Magnoliids 37 Monocots 67 Dicots 3 EXECUTIVE SUMMARY This report, State of New York City’s Plants 2018, is the first rankings of rare, threatened, endangered, and extinct species of what is envisioned by the Center for Conservation Strategy known from New York City, and based on this compilation of The New York Botanical Garden as annual updates thirteen percent of the City’s flora is imperiled or extinct in New summarizing the status of the spontaneous plant species of the York City. five boroughs of New York City. This year’s report deals with the City’s vascular plants (ferns and fern allies, gymnosperms, We have begun the process of assessing conservation status and flowering plants), but in the future it is planned to phase in at the local level for all species. -
Extended Phylogeny of Aquilegia: the Biogeographical and Ecological Patterns of Two Simultaneous but Contrasting Radiations
Plant Syst Evol (2010) 284:171–185 DOI 10.1007/s00606-009-0243-z ORIGINAL ARTICLE Extended phylogeny of Aquilegia: the biogeographical and ecological patterns of two simultaneous but contrasting radiations Jesu´s M. Bastida • Julio M. Alca´ntara • Pedro J. Rey • Pablo Vargas • Carlos M. Herrera Received: 29 April 2009 / Accepted: 25 October 2009 / Published online: 4 December 2009 Ó Springer-Verlag 2009 Abstract Studies of the North American columbines respective lineages. The genus originated between 6.18 (Aquilegia, Ranunculaceae) have supported the view that and 6.57 million years (Myr) ago, with the main pulses of adaptive radiations in animal-pollinated plants proceed diversification starting around 3 Myr ago both in Europe through pollinator specialisation and floral differentiation. (1.25–3.96 Myr ago) and North America (1.42–5.01 Myr However, although the diversity of pollinators and floral ago). The type of habitat occupied shifted more often in morphology is much lower in Europe and Asia than in the Euroasiatic lineage, while pollination vectors shifted North America, the number of columbine species is more often in the Asiatic-North American lineage. similar in the three continents. This supports the Moreover, while allopatric speciation predominated in the hypothesis that habitat and pollinator specialisation have European lineage, sympatric speciation acted in the North contributed differently to the radiation of columbines in American one. In conclusion, the radiation of columbines different continents. To establish the basic background to in Europe and North America involved similar rates of test this hypothesis, we expanded the molecular phylog- diversification and took place simultaneously and inde- eny of the genus to include a representative set of species pendently. -
Ornamental Grasses for Kentucky Landscapes Lenore J
HO-79 Ornamental Grasses for Kentucky Landscapes Lenore J. Nash, Mary L. Witt, Linda Tapp, and A. J. Powell Jr. any ornamental grasses are available for use in resi- Grasses can be purchased in containers or bare-root Mdential and commercial landscapes and gardens. This (without soil). If you purchase plants from a mail-order publication will help you select grasses that fit different nursery, they will be shipped bare-root. Some plants may landscape needs and grasses that are hardy in Kentucky not bloom until the second season, so buying a larger plant (USDA Zone 6). Grasses are selected for their attractive foli- with an established root system is a good idea if you want age, distinctive form, and/or showy flowers and seedheads. landscape value the first year. If you order from a mail- All but one of the grasses mentioned in this publication are order nursery, plants will be shipped in spring with limited perennial types (see Glossary). shipping in summer and fall. Grasses can be used as ground covers, specimen plants, in or near water, perennial borders, rock gardens, or natu- Planting ralized areas. Annual grasses and many perennial grasses When: The best time to plant grasses is spring, so they have attractive flowers and seedheads and are suitable for will be established by the time hot summer months arrive. fresh and dried arrangements. Container-grown grasses can be planted during the sum- mer as long as adequate moisture is supplied. Cool-season Selecting and Buying grasses can be planted in early fall, but plenty of mulch Select a grass that is right for your climate. -
Ornamental Grasses for the Midsouth Landscape
Ornamental Grasses for the Midsouth Landscape Ornamental grasses with their variety of form, may seem similar, grasses vary greatly, ranging from cool color, texture, and size add diversity and dimension to season to warm season grasses, from woody to herbaceous, a landscape. Not many other groups of plants can boast and from annuals to long-lived perennials. attractiveness during practically all seasons. The only time This variation has resulted in five recognized they could be considered not to contribute to the beauty of subfamilies within Poaceae. They are Arundinoideae, the landscape is the few weeks in the early spring between a unique mix of woody and herbaceous grass species; cutting back the old growth of the warm-season grasses Bambusoideae, the bamboos; Chloridoideae, warm- until the sprouting of new growth. From their emergence season herbaceous grasses; Panicoideae, also warm-season in the spring through winter, warm-season ornamental herbaceous grasses; and Pooideae, a cool-season subfamily. grasses add drama, grace, and motion to the landscape Their habitats also vary. Grasses are found across the unlike any other plants. globe, including in Antarctica. They have a strong presence One of the unique and desirable contributions in prairies, like those in the Great Plains, and savannas, like ornamental grasses make to the landscape is their sound. those in southern Africa. It is important to recognize these Anyone who has ever been in a pine forest on a windy day natural characteristics when using grasses for ornament, is aware of the ethereal music of wind against pine foliage. since they determine adaptability and management within The effect varies with the strength of the wind and the a landscape or region, as well as invasive potential. -
Exotic Plants in the Australian Alps Including a Case Study of the Ecology of Achillea Millefolium, in Kosciuszko National Park
Exotic Plants in the Australian Alps Including a Case Study of the Ecology of Achillea Millefolium, in Kosciuszko National Park Author Johnston, Frances Mary Published 2006 Thesis Type Thesis (PhD Doctorate) School School of Environmental and Applied Science DOI https://doi.org/10.25904/1912/3730 Copyright Statement The author owns the copyright in this thesis, unless stated otherwise. Downloaded from http://hdl.handle.net/10072/365860 Griffith Research Online https://research-repository.griffith.edu.au EXOTIC PLANTS IN THE AUSTRALIAN ALPS INCLUDING A CASE STUDY OF THE ECOLOGY OF ACHILLEA MILLEFOLIUM, IN KOSCIUSZKO NATIONAL PARK Frances Mary Johnston B.Sc. (Hons) A thesis submitted in fulfilment of the requirements of the Degree of Doctor of Philosophy School of Environmental and Applied Sciences Faculty of Environmental Sciences Griffith University Gold Coast August 2005 DECLARATION OF ORIGINALITY This work has not previously been submitted for a degree or diploma in any university. To the best of my knowledge and belief, this thesis represents my original research except where otherwise acknowledged in the text. Frances Johnston August 2005 FORWARD “In a small section of the garden a tiny weed spoke to the blooms that grew there. ‘Why,’ he asked, ‘does the gardener seek to kill me? Do I not have a right to life? Are my leaves not green, as yours are? Is it too much to ask that I be allowed to grow and see the sun?’ The blooms pondered on this, and decided to ask the gardener to spare the weed. He did so. Day by day the weed grew, stronger and stronger, taller and taller, its leaves covering the other plants, its roots spreading. -
Miscanthus Sinensis Sacchariflorus X Giganteus STERILE + =
Miscanthus: biofuels, invaders or both? Emily Heaton1, Allison Snow2, Maria Mariti2 and Catherine Bonin1 1Dept. Of Agronomy, Iowa State University 2Dept. of Evolution, Ecology, and Organismal Biology, The Ohio State University 2 36 Billion Gallons of Alternative Fuel… 2007 Energy Independ ence and Security Act What makes a good biomass crop? C4 photosynthesis Mobile Long canopy duration nutrients High water use efficiency & carbs to shoot Recycles nutrients to roots in spring Low input Clean burning translocated Sterile – non-invasive below ground as Winter standing shoot Easily removed senesces No known pests/diseases Easily managed Fig 1: Translocation increases nutrient use efficiency in perennial grasses What Are “The Canes”? - multiple interbreeding genera and species Examples include: SUGAR FIBER COLD/DISEASE Saccharum spp. Erianthus spp. Miscanthus spp. M. × giganteus: Naturally Occurring Hybrid Miscanthus Miscanthus Miscanthus sinensis sacchariflorus x giganteus STERILE + = Diploid Tetraploid Triploid 2n=2x=38 2n=4x=76 2n=3x=57 Distribution of three Asian Miscanthus species Original M. x giganteus hybrid collected in 1935 in Yokohama, Japan, cultivated in Denmark, then distributed throughout Europe and U.S. as an ornamental plant. Slide courtesy of Tom Voigt, UIUC. Giant Miscanthus (Miscanthus × 7 High Yielding (6-15 t/acre) giganteus) Sterile clone A higher Must be planted from yielding rhizomes alternative to New to US: 10’s to 100’s of switchgrass acres in some Widely planted in Europe: areas, especially thousands of acres the Used for heat and power Midwest with coal From Heaton et al. (2010) Advances in Botanical Research, 56, 76-137. First US field trial results in Illinois Field Bical Ltd. -
Ranunculaceae – Buttercup Family
RANUNCULACEAE – BUTTERCUP FAMILY Plant: mostly herbs, some woody vines or shrubs Stem: Root: Leaves: mostly alternate, sometimes opposite or whorled or basal; lobed or not lobed; if lobed then most often palmately, but occasionally pinnately, sometimes finely dissected – highly variable, sometimes even on the same plant; with or without stipules Flowers: mostly perfect, some dioecious; sepals 3-6, commonly 5; petals vary in number (3-23) but often 5, petals may be lacking and sepals are showy; stamens few to many; ovary superior, carpels few to very many, pistils one to many Fruit: mostly a dry capsule, seeds small, may be oily; rarely a berry Other: large family, sometimes confused with members of the Rose family (5 petals); Dicotyledons Group Genera: 60+ genera; locally Actaea (baneberry), Anemone (anemone or windflower), Aquilegia (columbine), Clematis, Isopyrum, Hepatica, Hydrastis, Ranunuculus (buttercup or crowfoot), Thalictrum (meadow-rue) WARNING – family descriptions are only a layman’s guide and should not be used as definitive Flower Morphology in the This is a large family often based on 5’s but Ranunculaceae (Buttercup Family) exceptions occur Examples of common genera White Baneberry [Doll’s-Eyes] Yellow Marsh Marigold [Cowslip] Goldenseal [Yellowroot] Actaea pachypoda Ell. Carolina [Wild Blue] Larkspur Caltha palustris L. var. palustris Delphinium carolinianum Walter Hydrastis canadensis L. Swamp Leather Flower [Eastern] False Rue Anemone Clematis crispa L. Devil-In-The-Bush [Love American Wood Anemone Enemion biternatum Raf. -In-A-Mist] Anemone quinquefolia L. [Isopyrum biternatum] Nigella damascena L. (Introduced) Doubtful [Rocket; Garden] Knight's-Spur [Larkspur] Round-lobed Hepatica [Liverleaf] Tall Buttercup Hepatica nobilis Schreber var. -
The Crowfoot Family in Ohio
THE CROWFOOT FAMILY IN OHIO. NELLIE F. HENDERSON. Ranunculaceae, Crowfoot Family. Perennial or annual herbs, or woody climbers, with acrid sap. Leaves usually alternate, sometimes opposite; simple or compound, with clasping or dilated base; stipules none. Flowers hypogynous, actinomorphic or sometimes zygomorphic, bispor- angiate or occasionally monosporangiate; perianth of similar segments or differentiated into calyx and corolla; capels usually separate; stamens numerous. Fruit an achene, follicle or berry. SYNOPSIS. I. Petals or sepals with a nectariferous pit, spur or tube. 1. Petals broad with a nectariferous pit; sepals not spurred. (I) Ranunculus; (2) Ficaria; (3) Batrichium. 2. Petals cup-shaped or narrow; sepals not spurred. (a) Pods sessile; leaves not trifoliate. (4) Trollius; (5) Helleborus; (6) Nigella. (b) Pods long stalked; leaves trifoliate. (7) Coptis. 3. Either petals or sepals spurred, or hooded; actinomorphic or zygomorphic. (8) Aquilegia; (9) Aconitum; (10) Delphinium. II. Sepals and petals without a nectar pit or spur; sepals usually petal-like. 1. Styles usually elongated, often very prominent in fruit; fruit an achene. (a) Sepals imbricated in the bud. (II) Anemone; (12) Hepatica. (b) Sepals valvate in the bud; leaves opposite. (13) Clematis; (14) yiorna. 2. Style short in fruit; fruit a many-seeded follicle, or a berry. (a) Flowers usually solitary, not racemose. (15) Caltha; (16) Hydrastis. (b) Flowers racemose. (17) Actaea; (18) Cimicifuga. 3. Style short in fruit; fruit an achene or a few-seeded follicle; leaves ternately compound or decompound. (19) Syndesmon; (20) Isopyrum; (21) Thalictrum. KEY TO THE GENERA. 1. Petals or sepals or both with a nectariferous cup, or spur; flowers frequently yellow. -
Non-Native Invasive Plants of the City of Alexandria, Virginia
March 1, 2019 Non-Native Invasive Plants of the City of Alexandria, Virginia Non-native invasive plants have increasingly become a major threat to natural areas, parks, forests, and wetlands by displacing native species and wildlife and significantly degrading habitats. Today, they are considered the greatest threat to natural areas and global biodiversity, second only to habitat loss resulting from development and urbanization (Vitousek et al. 1996, Pimentel et al. 2005). The Virginia Department of Conservation and Recreation has identified 90 non-native invasive plants that threaten natural areas and lands in Virginia (Heffernan et al. 2014) and Swearingen et al. (2010) include 80 plants from a list of nearly 280 non-native invasive plant species documented within the mid- Atlantic region. Largely overlapping with these and other regional lists are 116 species that were documented in the City of Alexandria, Virginia during vegetation surveys and natural resource assessments by the City of Alexandria Dept. of Recreation, Parks, and Cultural Activities (RPCA), Natural Lands Management Section. This list is not regulatory but serves as an educational reference informing those with concerns about non-native invasive plants in the City of Alexandria and vicinity, including taking action to prevent the further spread of these species by not planting them. Exotic species are those that are not native to a particular place or habitat as a result of human intervention. A non-native invasive plant is here defined as one that exhibits some degree of invasiveness, whether dominant and widespread in a particular habitat or landscape or much less common but long-lived and extremely persistent in places where it occurs. -
Response of Some Ornamental Flowers of Family Ranunculaceae to Sucrose Feeding
African Journal of Plant Science Vol. 4(9), pp. 346-352, September 2010 Available online at http://www.academicjournals.org/ajps ISSN 1996-0824 ©2010 Academic Journals Full Length Research Paper Response of some ornamental flowers of family Ranunculaceae to sucrose feeding Waseem Shahri*, Inayatullah Tahir, Sheikh Tajamul Islam and Mushtaq Ahmad Department of Botany, Plant Physiology and Biochemistry Research Laboratory, University of Kashmir, Srinagar- 190006, India. Accepted 30 July, 2010 The effect of different concentrations of sucrose on some ornamental flowers of family Ranunculaceae was examined. Sucrose was found to enhance vase life in cut spikes of Aquilegia vulgaris and Consolida ajacis cv. Violet blue; besides it improves blooming, fresh and dry mass of flowers. A. vulgaris and C. ajacis exhibits abscission type of flower senescence, while senescence in Ranunculus asiaticus cultivars is characterized by initial wilting followed by abscission at later stage. In isolated flowers of R. asiaticus cultivars, sucrose was found to be ineffective in delaying senescence and improving post-harvest performance. The study reveals that sucrose treatment shows varied response in different flowers of the same family and its effect appears to be related to ethylene-sensitivity of these flower systems. The paper recommends that more elaborate studies need to be conducted on other ethylene-sensitive flowers to make a generalized argument on relationship between sucrose and ethylene sensitivity. Key words: Aquilegia vulgaris, Consolida ajacis, Ranunculus asiaticus, abscission, wilting, sucrose, vase life, fresh mass, dry mass, senescence, Ranunculaceae. INTRODUCTION As long as a flowering shoot or an inflorescence is at the bud stage to open, which otherwise could not occur attached to a mother plant, nutrients are continuously naturally (Pun and Ichimura, 2003). -
Ranunculaceae Buttercup Family
Ranunculaceae buttercup family Larkspur, Columbine, Clematis and Anenome are common showy garden favourites belonging to this Page | 781 family. Mostly herbaceous, 2500 species have been described, organized in 51–88 genera. Flowers are regular, except in the Larkspur and Monkshood, where sepals resemble petals in form and colour. Petals may be present or absent. Stamens are numerous; pistils 1–many, developing fruit of various forms. The stamens may be modified into a staminode, producing nectar in some species. It may be large and showy as in the Columbine or inconspicuous. Leaves are alternate and compound, with some exceptions. Several are woody and some are even vines. Key to the species A. Plant a vine or climbing by clasping petioles. Clematis aa. Plant herbaceous, not climbing. B B. Leaves simple, shallowly lobed or serrate. C C. Leaves mostly 0.5–5cm wide; cauline leaves reduced; fruit an achene, Ranunculus many per plant. (Buttercups, in part). cc. Leaves kidney-shaped, 5–20cm wide; fruit a follicle, with many Caltha seeds. bb. Leaves compound, or deeply lobed. D D. Leaves all basal; plant <10cm tall. E E. Leaves trilobed, cut half or two-thirds to their bases, Hepatica margins smooth; flowers blue; sepals minute; rare species. ee. Leaves with 3 leaflets, toothed; flowers white, sepals Coptis absent; common in a variety of habitats. dd. Leaves both basal and cauline, or merely cauline; plant >10cm F tall. F. Cauline leaves 2–3, opposite or whorled; flowers 1– Anemone several, white; pedicels long; sepals petaloid. ff. Cauline leaves alternate, >3; flowers many, panicle; G yellow, pink, or purple; petals present.