The Typification of Cotoneaster Symondsii (Rosaceae)
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Shrub List for Brighton 2010
Shrub List For Brighton 2010 Large Shrubs 10’ -20’ Tall by 6’ – 25’ wide Acer ginnala Amur Maple Acer tataricum Tatarian Maple (better than Amur Maple) Acer grandidentatum Bigtooth Maple Amelanchier alnifolia Saskatoon Serviceberry Amelanchier canadensis Shadblow Serviceberry Caragana arborescens Siberian Peashrub Cercocarpus ledifolius Mountain Mahogany Cotoneaster lucidus Peking Cotoneaster Cowania mexicana Quince Bush, Cliffrose Crataefus ambigua Russian Hawthorn Forestiera neomexicana New Mexican Privet Hippophae rhamnoides Sea Buckthorn Juniperus species Juniper Kolkwitzia amabilis Beauty Bush Pinus mugo Mugo Pine species Prunus americana American Plum Prunus virginiana ‘Shubert’ Canada Red Chokecherry Ptelea trifoliata Wafer Ash or Hop tree Quercus gambelii Gambel Oak Rhus typhina Staghorn Sumac Robinia neomexicana New Mexico Locust Sambucus species Elders Shepherdia argentea Buffaloberry Syringa vulgaris Common Lilac Viburnum lantana Wayfaring Tree, Viburnum Medium Size Shrubs >10’ high by >8’ wide Amorpha fruticosa False Indigo Atriplex canescens Fourwing Saltbush Buddleia davidii Butterfly Bush Cercocarpus montanus Mountain Mahogany Chamaebatiaria millefolium Fernbush Chrysothamnus nauseosus Rubber Rabbitbrush Cornus sericea Redtwig Dogwood Cotinus coggygria Smoke Tree Cotoneaster species Cotoneaster Cytisus scoparius ‘Moonlight’ Moonlight Broom Euonymus alatus Burning Bush Forsythia x intermedia Forsythia Hibiscus syriacus Rose-of-Sharon Juniperus species Juniper Ligustrum vulgare Privet Lonicera species Honeysuckle Mahonia aquifolium Oregon Grape Holly Philadelphus species Mockorange Pyracantha coccinea Firethorn Physocarpus opulifolius Common Ninebark Prunus besseyi Western Sand Cherry Pyracantha coccinea species Firethorn Rhamnus frangula Glossy Buckthorn Ribes species Currant Sambucus species Elder Spiraea x vanhouttei Vanhouttei Spirea Symphoricarpos albus Snowberry Syringa meyeri „Palibin‟ Dwarf Korean Lilac Syringa patula „Miss Kim‟ Dwarf Lilac Viburnum species (dozens of different types) Small Size Shrubs > 5’ tall by >6. -
Conserving Europe's Threatened Plants
Conserving Europe’s threatened plants Progress towards Target 8 of the Global Strategy for Plant Conservation Conserving Europe’s threatened plants Progress towards Target 8 of the Global Strategy for Plant Conservation By Suzanne Sharrock and Meirion Jones May 2009 Recommended citation: Sharrock, S. and Jones, M., 2009. Conserving Europe’s threatened plants: Progress towards Target 8 of the Global Strategy for Plant Conservation Botanic Gardens Conservation International, Richmond, UK ISBN 978-1-905164-30-1 Published by Botanic Gardens Conservation International Descanso House, 199 Kew Road, Richmond, Surrey, TW9 3BW, UK Design: John Morgan, [email protected] Acknowledgements The work of establishing a consolidated list of threatened Photo credits European plants was first initiated by Hugh Synge who developed the original database on which this report is based. All images are credited to BGCI with the exceptions of: We are most grateful to Hugh for providing this database to page 5, Nikos Krigas; page 8. Christophe Libert; page 10, BGCI and advising on further development of the list. The Pawel Kos; page 12 (upper), Nikos Krigas; page 14: James exacting task of inputting data from national Red Lists was Hitchmough; page 16 (lower), Jože Bavcon; page 17 (upper), carried out by Chris Cockel and without his dedicated work, the Nkos Krigas; page 20 (upper), Anca Sarbu; page 21, Nikos list would not have been completed. Thank you for your efforts Krigas; page 22 (upper) Simon Williams; page 22 (lower), RBG Chris. We are grateful to all the members of the European Kew; page 23 (upper), Jo Packet; page 23 (lower), Sandrine Botanic Gardens Consortium and other colleagues from Europe Godefroid; page 24 (upper) Jože Bavcon; page 24 (lower), Frank who provided essential advice, guidance and supplementary Scumacher; page 25 (upper) Michael Burkart; page 25, (lower) information on the species included in the database. -
Cotoneaster Apiculatus
Cotoneaster apiculatus - Cranberry Cotoneaster (Rosaceae) ------------------------------------------------------------------------------------------------------- Cotoneaster apiculatus is a low arching to mounding Fruits shrub, with glossy small leaves and prominent -red, maturing in late Aug. and a very effective globular red fruits. Cranberry Cotoneaster is often contrast in late summer and early autumn while the utilized as an edging or facer shrub or as a tall foliage is still a glossy dark green groundcover. -0.25" diameter and persistent into early winter -effective display when in mass plantings FEATURES Twigs Form -red-purple with persistent pubescence -low sprawling -older stems olive-brown and lenticeled deciduous shrub or -branches continuously arching with numerous side moderately tall branchlets woody groundcover -buds very small -maturing at 1.5' tall Trunk x 5' wide -not applicable -arching mound and spreading mound USAGE growth habit, with Function branches sometimes -shrub or groundcover effective as an edging, facer, rooting as they touch the ground embankment, mass planting, low barrier, foundation, wall, or -slow growth rate raised planter (short cascading effect) woody plant Culture Texture -full sun to partial shade -fine texture in foliage but medium when bare -prefers moist, well-drained soils but is very urban -open density in foliage and when bare stress tolerant, including poor soils, soil pHs, drought, Assets pruning, salt spray, and some soil compaction -lustrous dark green foliage -propagated by rooted cuttings -
Ultra Competitive Plants
Ultra Competitive Plants Data Sheet No 2: Cotoneaster species Cotoneaster species are widely used by landscape architects as both trees and shrubs. Whilst most of these species are useful and attractive plants, there are however, five species that pose significant problems for designed and ‘natural’ environments throughout the UK. The chief problem is that they have the potential to spread widely and outcompete native flora in areas such as heaths, exposed hillsides and dune systems. As such their use should be carefully considered and actions prescribed in management plans to ensure that they do not escape the designed environment. Relevant legislation All five invasive species of Cotoneaster are listed on Schedule 9 of the Wildlife and Countryside Act in England and Wales and it is therefore an offence to plant or otherwise cause to grow these species in the wild. However, some Schedule 9 plants are widely available in nurseries but are rarely advertised as such and landscape architects should ensure that they are aware of the implications of using these plants inappropriately or without understanding the risks. In addition, many Cotoneaster species in addition to the five species identified here are monitored by the Non Native Species Secretariat, whilst many species meet the criteria for being listed as an Article 4 species in the EU Invasive Alien Species Regulation and as such, may soon be subject to these conditions. In any case, as a signatory to the Convention on Biological Diversity, the UK has a duty to manage pathways to prevent the introduction and establishment of alien invasive species under Article 9 of the Aichi Biodiversity Targets. -
Alien Flora of Europe: Species Diversity, Temporal Trends, Geographical Patterns and Research Needs
Preslia 80: 101–149, 2008 101 Alien flora of Europe: species diversity, temporal trends, geographical patterns and research needs Zavlečená flóra Evropy: druhová diverzita, časové trendy, zákonitosti geografického rozšíření a oblasti budoucího výzkumu Philip W. L a m b d o n1,2#, Petr P y š e k3,4*, Corina B a s n o u5, Martin H e j d a3,4, Margari- taArianoutsou6, Franz E s s l7, Vojtěch J a r o š í k4,3, Jan P e r g l3, Marten W i n t e r8, Paulina A n a s t a s i u9, Pavlos A n d r i opoulos6, Ioannis B a z o s6, Giuseppe Brundu10, Laura C e l e s t i - G r a p o w11, Philippe C h a s s o t12, Pinelopi D e l i p e t - rou13, Melanie J o s e f s s o n14, Salit K a r k15, Stefan K l o t z8, Yannis K o k k o r i s6, Ingolf K ü h n8, Hélia M a r c h a n t e16, Irena P e r g l o v á3, Joan P i n o5, Montserrat Vilà17, Andreas Z i k o s6, David R o y1 & Philip E. H u l m e18 1Centre for Ecology and Hydrology, Hill of Brathens, Banchory, Aberdeenshire AB31 4BW, Scotland, e-mail; [email protected], [email protected]; 2Kew Herbarium, Royal Botanic Gardens Kew, Richmond, Surrey, TW9 3AB, United Kingdom; 3Institute of Bot- any, Academy of Sciences of the Czech Republic, CZ-252 43 Průhonice, Czech Republic, e-mail: [email protected], [email protected], [email protected], [email protected]; 4Department of Ecology, Faculty of Science, Charles University, Viničná 7, CZ-128 01 Praha 2, Czech Republic; e-mail: [email protected]; 5Center for Ecological Research and Forestry Applications, Universitat Autònoma de Barcelona, 08193 Bellaterra, Spain, e-mail: [email protected], [email protected]; 6University of Athens, Faculty of Biology, Department of Ecology & Systematics, 15784 Athens, Greece, e-mail: [email protected], [email protected], [email protected], [email protected], [email protected]; 7Federal Environment Agency, Department of Nature Conservation, Spittelauer Lände 5, 1090 Vienna, Austria, e-mail: [email protected]; 8Helmholtz Centre for Environmental Research – UFZ, Department of Community Ecology, Theodor-Lieser- Str. -
15. PHOTINIA Lindley, Trans. Linn. Soc. London 13: 96, 103. 1821.1 石楠属 Shi Nan Shu Lu Lingdi (陆玲娣 Lu Ling-Ti); Stephen A
Flora of China 9: 121–137. 2003. 15. PHOTINIA Lindley, Trans. Linn. Soc. London 13: 96, 103. 1821.1 石楠属 shi nan shu Lu Lingdi (陆玲娣 Lu Ling-ti); Stephen A. Spongberg Pourthiaea Decaisne. Trees or shrubs, deciduous or evergreen. Winter buds small; scales imbricate, few. Leaves alternate, simple, papery or leathery, venation camptodromous, margin serrate, rarely entire, shortly petiolate; stipules present, usually subulate. Inflorescences terminal, umbellate or corymbose, rarely shortly paniculate, many flowered, sometimes flowers 2- or 3-clustered or solitary. Hypanthium cupular or campanulate to cylindric, adnate to ovary or free near apex. Sepals 5, persistent, short. Petals 5, contorted or imbricate in bud, base clawed. Stamens usually ca. 20. Carpels 2–5, rarely 1; ovary semi-inferior, (1 or)2–5-loculed, in fruit free apically or to 1/3 length; styles (1 or)2–5, free or ± connate, short, dilated apically; stigmas truncate; ovules 2 per locule, erect. Fruit a pome, globose, ovoid, or ellipsoid, somewhat fleshy, (1- or)2–5-loculed, free from calyx only near apex or to 1/3 length, with persistent, incurved sepals; carpel crustaceous or membranous, each locule 1- or 2-seeded; seeds erect, testa leathery; cotyledons plano-convex. About 60 species: E, S, and SE Asia, also in Mexico; 43 species (32 endemic) in China. Wu Zhengyi (editor’s note) believes that Pourthiaea is morphologically distinct from Photinia and should be treated as a separate genus. Many species of Photinia are ornamental trees and shrubs with large lustrous leaves and attractive white flowers in the spring followed by red fruits in the autumn. -
Relative Ranking of Ornamental Flower Plants to Foraging Honey Bees (With Notes on Favorability to Bumble Bees)
Relative Ranking of Ornamental Flower Plants to Foraging Honey Bees (With Notes on Favorability to Bumble Bees) Whitney Cranshaw Colorado State University Observations were made during the 2007-2009 growing seasons on the relative attractiveness of various flowering ornamental plants to honey bees (Apis mellifera). This information was collected so that honey bee favorability - or lack of favorability - may be considered in plant selection. The study was conducted by repeated visits to public garden plantings in Larimer, Denver, Adams, and Cheyenne counties. Gardens were chosen that had large mass plantings of numerous flowering plants so that comparisons could be made and included the Denver Botanic Garden, gardens at Colorado State University (PERC, Flower Demonstration Planting), Welby Gardens, and Cheyenne Botanic Garden. These sites also were chosen because plantings had identification labeling. Plantings were visited between 2 and 12 times between mid-June and mid-September. Evaluations were made by examining plants that were in flower for the presence of honey bees. A planting was then given a relative ranking based on honey bee numbers. A 0-3 scale was used: 3 - Heavily visited by foraging honey bees 2 - Moderately visited by honey bees and foraged 1 - Honey bees seen occasionally visiting flowers 0 - Honey bees do not forage at these flowers Data were collected from a total of 319 different plant entries durig this study. Variation in rankings between dates did occur; where this occurred from multiple ratings the final ranking was rounded up to a whole number. Numerous other bees and other insects were commonly seen on many plants. -
Distribution of Amelanchier Ovalis Medik. in the Romanian Carpathians – a Critical Overview
STUDIA UNIVERSITATIS BABEù-BOLYAI BIOLOGIA, LXI, 2, 2016 (p. 81-94) Distribution of Amelanchier ovalis Medik. in the Romanian Carpathians – a critical overview Adrian Indreica1, Mihai Pu܈ca܈2 and Attila Bartók3 SUMMARY. This study proposes a critical analysis of the distribution of the rare plant species Amelanchier ovalis Medik. in the Romanian Carpathians.The species was mentioned as sporadically distributed in this part of Carpathians, but we found no evidence that the plant was ever collected and deposited in public herbaria. Besides herbarium material, a critical analysis of available botanical literature concurred to the same conclusion: the presence of Amelanchier ovalis in all previously mentioned localities in the Romanian Carpathians can not be supported by any concrete data and, therefore, can be considered as doubtful. The paper reports the recent discovery of Amelanchier ovalis in a new area in the Eastern Carpathians (Vrancea Mountains, Putna-Vrancea Natural Park). A detailed description of plant communities in which the species grows is also provided. Additionally, new sites with Hieracium telekianum Boros & Lengyel (Eastern Carpathian endemic and rare species) are also reported in Vrancea Mountains. Keywords: Amelanchier ovalis, Chorology, Red Book, Romanian Carpathians, threatened species Introduction Romanian flora includes many species whose presence is uncertain and should be reconfirmed (e.g. Dianthus diutinus Kit., Euphorbia paralias L., Thesium ebracteatum Hayne, Ledum palustre L., Ophrys fusca Link, Osmunda regalis L., etc.) (Sârbu et al. 2013). Two of these species (Saussurea porcii Degen and Jasione orbiculata Griseb. ex Velen.) have been recently reconfirmed in Rodna (Eastern Carpathians) and, respectively, in Retezat Mountains (Southern Carpathians) (Mátis et al., 2014; Bartók 2014). -
Cotoneaster Franchetii
Cotoneaster franchetii COMMON NAME Cotoneaster, Franchet’s Cotoneaster FAMILY Rosaceae FLORA CATEGORY Vascular – Exotic STRUCTURAL CLASS Trees & Shrubs - Dicotyledons BRIEF DESCRIPTION Widely branched shrub with arching branchlets, foliage conspicuously grey from a distance (young leaves densely hairy on both surfaces and remaining white-felted below when mature). Flowers with pink erect petals. Fruit orange with 3-5 pyrenes. HABITAT Cotoneaster franchetii. Photographer: Nic Terrestrial. Outcompetes native shrub species in a wide variety of Singers habitats. Usually dry forest and shrubland up to 300 m, forest margins, dry rangeland, bluffs, rocky sites, slips, riverbeds. FEATURES Evergreen shrub up to c. 3 m high; stems spreading and often somewhat arching; young shoots pale buff-tomentose, later becoming dark reddish brown. Leaves up to 35 x 18 mm, more or less shining and finely pilose with impressed veins above, usually with white to grey woolly tomentum (rarely pale buff) below. Flowers in clusters of 7-15 scattered along branches, Petals erect and pink. Fruit ellipsoid, oblong-obovoid, obovoid, or subglobose, 5-9 mm long, scarlet or orange scarlet. SIMILAR TAXA Cotoneaster franchetii. Photographer: Colin Has been confused with C. pannosus, but that species has flowers with Ogle spreading petals and almost always has 2 pyrenes (‘seeds’) per fruit, whereas C. franchetii has flowers with erect petals and mostly has 3 (up to 5) pyrenes per fruit. FLOWERING November, December, January FLOWER COLOURS Red/Pink LIFE CYCLE Perennial. Very long lived. Large numbers of viable seed are produced in each fruit. Fruit are readily dispersed by birds. YEAR NATURALISED 1958 ORIGIN China REASON FOR INTRODUCTION Ornamental TOLERANCES Very tolerant of damp and drought, hot and cold, salt, and a range of soils. -
Cotoneaster Franchetii Boiss.; Orange Cotoneaster Cotoneaster Lacteus W.W
A WEED REPORT from the book Weed Control in Natural Areas in the Western United States This WEED REPORT does not constitute a formal recommendation. When using herbicides always read the label, and when in doubt consult your farm advisor or county agent. This WEED REPORT is an excerpt from the book Weed Control in Natural Areas in the Western United States and is available wholesale through the UC Weed Research & Information Center (wric.ucdavis.edu) or retail through the Western Society of Weed Science (wsweedscience.org) or the California Invasive Species Council (cal-ipc.org). Cotoneaster franchetii Boiss.; orange cotoneaster Cotoneaster lacteus W.W. Smith; Parney’s cotoneaster Cotoneaster pannosus Franch.; silverleaf cotoneaster Cotoneasters Family: Rosaceae C. franchetii Range: Coastal areas of California, Oregon, and Washington. Habitat: Disturbed places, mixed evergreen forest, coastal scrub, and grassland, often near residential areas. Origin: Introduced as ornamental plants from China and escaped to become invasive in coastal regions. Impacts: On occasion, populations can become dense and crowd out native species. However, fruit likely provide a food source for some bird species. California Invasive Plant Council (Cal-IPC) Inventory: All three species are Moderate Invasiveness C. lacteus Cotoneasters are evergreen to semi-evergreen shrubs usually C. pannosus less than 10 ft tall, but occasionally taller. All species have simple alternate leaves and distinctive orange or red berry-like fruits. The upper surfaces of the leaves are generally dull with few or no hairs. The lower surface is usually covered with woolly hairs, but can lack hairs. Flowers are white in both Parney’s and silverleaf cotoneaster, but pink to rose in orange cotoneaster. -
Crataegus (Hawthorn)
nysipm.cornell.edu 2019 Search for this title at the NYSIPM Publications collection: ecommons.cornell.edu/handle/1813/41246 Disease and Insect Resistant Ornamental Plants Mary Thurn, Elizabeth Lamb, and Brian Eshenaur New York State Integrated Pest Management Program, Cornell University CRATAEGUS Hawthorn pixabay.com Crataegus is a large genus of shrubs and small trees in the rose family commonly known as hawthorn. This popular ornamental has showy pink or white flowers in spring and colorful berry-like fruit. Some species also have long thorns that provide protection for wildlife but may be a hazard in the landscape–thornless cultivars are available. Like other rosaceous plants, hawthorns are sus- ceptible to a number of diseases including fire blight, scab, leaf spot and several types of rust. Insect pests include lace bugs and leaf miners. DISEASES Cedar Rust diseases on hawthorn, which include hawthorn rust and quince rust, are caused by sev- eral fungi in the genus Gymnosporangium that spend part of their life cycle on Eastern red cedar (Juni- perus virginiana) and other susceptible junipers, and another part of their life cycle on plants in the rose family, especially Malus and Crataegus. Since two hosts are required for these fungi to complete their life cycle, one way to reduce disease problems is to avoid planting alternate hosts near each other. Hawthorn Rust, caused by Gymnosporangium globosum, is a significant concern for Crataegus spp. in the Northeast (7). Hawthorns are the main broadleaved host for this rust, and yellow-orange leaf spots are the most common symptom. (8). With severe infections, foliage may turn bright yellow and drop prematurely (15). -
An Overview of the Genus Cotoneaster (Rosaceae): Phytochemistry, Biological Activity, and Toxicology
antioxidants Review An Overview of the Genus Cotoneaster (Rosaceae): Phytochemistry, Biological Activity, and Toxicology Agnieszka Kicel Department of Pharmacognosy, Faculty of Pharmacy, Medical University of Lodz, 1 Muszynskiego, 90-151 Lodz, Poland; [email protected] Received: 18 September 2020; Accepted: 13 October 2020; Published: 16 October 2020 Abstract: Traditional herbal medicines have become a subject of global importance with both medical and economic implications. The regular consumption of herbal drugs has led to serious concerns regarding their quality, effectiveness, and safety. Thus, relevant scientific evidence has become an important criterion for the acceptance of traditional health claims. The genus Cotoneaster Medikus provides numerous species traditionally used in Asian medicine for the treatment of haemorrhoids, diabetes, and cardiovascular diseases. This review summarises the achievements of modern research on the Cotoneaster taxa, including ethnobotany, phytochemistry, pharmacology, and toxicology. To date, more than 90 compounds have been isolated or analytically identified in Cotoneaster leaves, fruits, flowers or twigs. These phytochemicals are categorised into flavonoids, procyanidins, phenolic acids, cotonefurans, cyanogenic glycosides, triterpenes, sterols, fatty acids, volatile compounds, and carbohydrates, and many of them are responsible for Cotoneaster pharmacological properties including antioxidant, anti-inflammatory, antimicrobial, antiparasitic, hepatoprotective, anti-diabetic or anti-dyslipidaemic