China: a Rich Flora Needed of Urgent Conservationprovided by Digital.CSIC
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Alternanthera Philoxeroides (Mart.) Griseb
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). Alternanthera philoxeroides (Mart.) Griseb. Alligatorweed Family: Amaranthaceae Range: Mainly in the southeastern states, but also in California. Habitat: Shallow water in ditches, marshes, pond margins, and slow- moving waterways. May also be found terrestrially in wet soils. It can tolerate saline conditions up to 10% salt by volume. Alligatorweed requires a warm summer growing condition but can survive cold winters provided there are no prolonged periods of freezing temperatures. Origin: Native to South America. Impact: Alligatorweed forms dense floating mats on the surface of water Photo courtesy of Richard Old that decrease light penetration and change the natural ecology at the site. It also competes with native vegetation, can cause flooding, and has the potential to create anoxic conditions, increase mosquito breeding, and harbor diseases. Western states listed as Noxious Weed: Arizona, California California Invasive Plant Council (Cal-IPC) Inventory: High Invasiveness (Alert) Alligatorweed is an aquatic perennial that also has a terrestrial form. The aquatic form roots in shallow water and rarely grows in water deeper than 6 ft. -
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THE SPECIES Clerodendrum myricoides (Rotheca myricoides) Verbenaceae Indigenous STANDARDlTRADE NAME: Butterfly bush. COMMON NAMES: Boran: Mara sisa; Kamba: Kiteangwai, Muvweia; Kikuyu: Munjugu; Kipsigis: Chesamisiet, Obetiot; Luhya (Bukusu): Kumusilangokho; Luhya: Shisilangokho; Luo: Kurgweno, Okwergweno, Okwero, Okworo, Oseke, Sangla; Maasai: Olmakutukut; Marakwet: Chebobet, Chesagon; Samburu: Makutukuti; Tugen: Gobetie. DESCRIPTION: A small shrub up to 3.5 m, much branched from the base and often with some branches scrambling through other plants. The leaves and stem have a distinctive smell when crushed. LEA VES: Opposite or in whods, simple, ovate, margin toothed or, rarely, entire, up to 12 cm long but usually smaller, without hairs and almost stalkless. FLOWERS: Blue or purple, sweetly scented, conspicuous, irregular, 2 petals shaped like butterfly wings. FRUIT: Small rounded berry, black when ripe. ECOLOGY: Found from Sudan and Ethiopia south to Zimba bwe. A common shrub in forest edges, bushland, moun tain scrub, wooded grassland and in secondary vegeta tion, 1,500-2,400 m. Common in rocky places. Agroclimatic Zone Ill. Flowers may occur any time of the year. USES: Arrows, medicine (leaves, stem, roots), bee forage, ornamental, ceremonial. PROPAGATION: Propagation is easy. Cuttings and seedlings can be used, as well as root cuttings or root suckers produced from exposed or injured roots. REMARKS: There are close to two dozen Clerodendrum species in Kenya. C. myricoides is the commonest. Other common species are C. johnstonii (Kamba: Muteangwai; Kikuyu: Muringo; Luhya; Lusala; Marakwet: Jersegao; Meru: Kiankware), which can be a shrub or liana that climbs with the remains of leaf petioles. Flowers are white and the usually galled fruits orange to black. -
Chamaecyparis Lawsoniana: Lawson Falsecypress1 Edward F
ENH313 Chamaecyparis lawsoniana: Lawson Falsecypress1 Edward F. Gilman and Dennis G. Watson2 Introduction General Information Often seen at 40 to 60 feet tall by 15 feet wide in its culti- Scientific name: Chamaecyparis lawsoniana vated form, this North American native can soar to heights Pronunciation: kam-eh-SIP-uh-riss law-so-nee-AY-nuh of 100 to 150 feet in the wild. The massive, thick trunk and Common name(s): Lawson falsecypress, Port Orford cedar formal, upright, conical silhouette is softened by the gently Family: Cupressaceae weeping tips of the short, upright branches. The flattened, USDA hardiness zones: 5B through 7B (Fig. 2) dark blue-green branchlets have a delicate, almost fern-like Origin: native to North America appearance, and are nicely complemented by the rough, Invasive potential: little invasive potential deeply furrowed, reddish-brown bark. Available in a wide Uses: specimen; screen; bonsai variety of forms and bluish foliage colors, Lawson falsecy- Availability: not native to North America press still remains today an important timber trees from the Pacific Northwest. But it is rare in the nursery trade and probably not well adapted to most landscapes. Figure 2. Range Description Height: 40 to 60 feet Spread: 15 to 25 feet Crown uniformity: symmetrical Figure 1. Mature Chamaecyparis lawsoniana: Lawson Falsecypress 1. This document is ENH313, one of a series of the Environmental Horticulture, UF/IFAS Extension. Original publication date November 1993. Reviewed May 2014. Visit the EDIS website at http://edis.ifas.ufl.edu. 2. Edward F. Gilman, professor, Environmental Horticulture Department; Dennis G. Watson, former associate professor, Agricultural Engineering Department, UF/IFAS Extension, Gainesville FL 32611. -
Non-Native Trees and Large Shrubs for the Washington, D.C. Area
Green Spring Gardens 4603 Green Spring Rd ● Alexandria ● VA 22312 Phone: 703-642-5173 ● TTY: 703-803-3354 www.fairfaxcounty.gov/parks/greenspring NON - NATIVE TREES AND LARGE SHRUBS FOR THE WASHINGTON, D.C. AREA Non-native trees are some of the most beloved plants in the landscape due to their beauty. In addition, these trees are grown for the shade, screening, structure, and landscape benefits they provide. Deciduous trees, whose leaves die and fall off in the autumn, are valuable additions to landscapes because of their changing interest throughout the year. Evergreen trees are valued for their year-round beauty and shelter for wildlife. Evergreens are often grouped into two categories, broadleaf evergreens and conifers. Broadleaf evergreens have broad, flat leaves. They also may have showy flowers, such as Camellia oleifera (a large shrub), or colorful fruits, such as Nellie R. Stevens holly. Coniferous evergreens either have needle-like foliage, such as the lacebark pine, or scale-like foliage, such as the green giant arborvitae. Conifers do not have true flowers or fruits but bear cones. Though most conifers are evergreen, exceptions exist. Dawn redwood, for example, loses its needles each fall. The following are useful definitions: Cultivar (cv.) - a cultivated variety designated by single quotes, such as ‘Autumn Gold’. A variety (var.) or subspecies (subsp.), in contrast, is found in nature and is a subdivision of a species (a variety of Cedar of Lebanon is listed). Full Shade - the amount of light under a dense deciduous tree canopy or beneath evergreens. Full Sun - at least 6 hours of sun daily. -
Chloroplast in Plant-Virus Interaction
REVIEW published: 04 October 2016 doi: 10.3389/fmicb.2016.01565 Chloroplast in Plant-Virus Interaction Jinping Zhao 1, 2, Xian Zhang 3, Yiguo Hong 3 and Yule Liu 1* 1 MOE Key Laboratory of Bioinformatics, Center for Plant Biology, Tsinghua-Peking Joint Center for Life Sciences, School of Life Sciences, Tsinghua University, Beijing, China, 2 State Key Laboratory Breeding Base for Sustainable Control of Pest and Disease, Key Laboratory of Biotechnology in Plant Protection, Institute of Virology and Biotechnology, Zhejiang Academy of Agricultural Sciences, Hangzhou, China, 3 Research Centre for Plant RNA Signaling, School of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou, China In plants, the chloroplast is the organelle that conducts photosynthesis. It has been known that chloroplast is involved in virus infection of plants for approximate 70 years. Recently, the subject of chloroplast-virus interplay is getting more and more attention. In this article we discuss the different aspects of chloroplast-virus interaction into three sections: the effect of virus infection on the structure and function of chloroplast, the role of chloroplast in virus infection cycle, and the function of chloroplast in host defense against viruses. In particular, we focus on the characterization of chloroplast protein-viral protein interactions that underlie the interplay between chloroplast and virus. It can be summarized that chloroplast is a common target of plant viruses for viral pathogenesis or propagation; and conversely, chloroplast and its components also can play active Edited by: Nobuhiro Suzuki, roles in plant defense against viruses. Chloroplast photosynthesis-related genes/proteins Okayama University, Japan (CPRGs/CPRPs) are suggested to play a central role during the complex chloroplast-virus Reviewed by: interaction. -
Haloxylon Ammodendron (Chenopodiaceae)
Complete Chloroplast Genome Sequence of Holoparasite Cistanche deserticola (Orobanchaceae) Reveals Gene Loss and Horizontal Gene Transfer from Its Host Haloxylon ammodendron (Chenopodiaceae) Xi Li1., Ti-Cao Zhang1., Qin Qiao1, Zhumei Ren2, Jiayuan Zhao1, Takahiro Yonezawa1, Masami Hasegawa1, M. James C Crabbe3, Jianqiang Li4*, Yang Zhong1,5* 1 Ministry of Education Key Laboratory for Biodiversity Science and Ecological Engineering, School of Life Sciences, Fudan University, Shanghai, China, 2 College of Life Science and Technology, Shanxi University, Taiyuan, China, 3 Faculty of Creative Arts, Technologies and Science, Institute of Biomedical, Environmental Science and Technology, University of Bedfordshire, Luton, United Kingdom, 4 Wuhan Botanical Garden, Chinese Academy of Sciences, Wuhan, China, 5 Institute of Biodiversity Science and Geobiology, Tibet University, Lhasa, China Abstract Background: The central function of chloroplasts is to carry out photosynthesis, and its gene content and structure are highly conserved across land plants. Parasitic plants, which have reduced photosynthetic ability, suffer gene losses from the chloroplast (cp) genome accompanied by the relaxation of selective constraints. Compared with the rapid rise in the number of cp genome sequences of photosynthetic organisms, there are limited data sets from parasitic plants. Principal Findings/Significance: Here we report the complete sequence of the cp genome of Cistanche deserticola,a holoparasitic desert species belonging to the family Orobanchaceae. The cp genome of C. deserticola is greatly reduced both in size (102,657 bp) and in gene content, indicating that all genes required for photosynthesis suffer from gene loss and pseudogenization, except for psbM. The striking difference from other holoparasitic plants is that it retains almost a full set of tRNA genes, and it has lower dN/dS for most genes than another close holoparasitic plant, E. -
Catalogue of Conifers
Archived Document Corporate Services, University of Exeter Welcome to the Index of Coniferaes Foreword The University is fortunate in possessing a valuable collection of trees on its main estate. The trees are planted in the grounds of Streatham Hall which was presented in 1922 to the then University college of the South West by the late Alderman W. H. Reed of Exeter. The Arboretum was begun by the original owner of Streatham Hall, R. Thornton West, who employed the firm of Veitches of Exeter and London to plant a very remarkable collection of trees. The collection is being added to as suitable material becomes available and the development of the Estate is being so planned as not to destroy the existing trees. The present document deals with the Conifer species in the collection and gives brief notes which may be of interest to visitors. It makes no pretence of being more than a catalogue. The University welcomes interested visitors and a plan of the relevant portion of the Estate is given to indicate the location of the specimens. From an original printed by James Townsend and Sons Ltd, Price 1/- Date unknown Page 1 of 34 www.exeter.ac.uk/corporateservices Archived Document Corporate Services, University of Exeter Table of Contents The letters P, S, etc., refer to the section of the Estate in which the trees are growing. (Bot. indicates that the specimens are in the garden of the Department of Botany.) Here's a plan of the estate. The Coniferaes are divided into five families - each of which is represented by one or more genera in the collection. -
Wood Anatomy of Calycanthaceae Sherwin Carlquist
Aliso: A Journal of Systematic and Evolutionary Botany Volume 10 | Issue 3 Article 6 1983 Wood Anatomy of Calycanthaceae Sherwin Carlquist Follow this and additional works at: http://scholarship.claremont.edu/aliso Part of the Botany Commons Recommended Citation Carlquist, Sherwin (1983) "Wood Anatomy of Calycanthaceae," Aliso: A Journal of Systematic and Evolutionary Botany: Vol. 10: Iss. 3, Article 6. Available at: http://scholarship.claremont.edu/aliso/vol10/iss3/6 ALISO 10(3), 1983, pp. 427-441 WOOD ANATOMY OF CALYCANTHACEAE: ECOLOGICAL AND SYSTEMATIC IMPLICATIONS Sherwin Carlquist INTRODUCTION Wood anatomy of Calycanthaceae has not been studied as a unit. Wood features ofthe family have been summarized by Metcalfe and Chalk (1950); various authors have mentioned one or more traits in studies dealing with Calycanthaceae (e.g., Wilson 1979) or other families (e.g., Garratt 1934). In view of recent interest in Idiospermum australiense (Diels) Blake, a new comparative study is needed. One goal of the present study is clarification of relationships of Idiospermum to Calycanthus and Chimonanthus. Wood anatomy of Idiospermum was described by Blake ( 1972) and Wilson ( 1979); a new description is offered here to provide more quantitative data. De scriptions of the wood of Calycanthus and Chimonanthus provided here incorporate such quantitative data, but also modify earlier descriptions with respect to some important qualitative features. Material of the recently de scribed genus Sinocalycanthus (Cheng and Chan 1964) was not available, although the description of that genus suggests it is not strongly different from Calycanthus or Chimonanthus. The present study incorporates material of Calycanthus floridus L. var. floridus, C. -
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 -
Determination of Bergenin in Different Parts of Bergenia Ciliata Using a Validated RP-HPLC Method
Natural Product Sciences 27(1) : 54-59 (2021) https://doi.org/10.20307/nps.2021.27.1.54 Determination of Bergenin in Different Parts of Bergenia ciliata using a Validated RP-HPLC Method Ejaz Ali1,*, Khalid Hussain1, Nadeem Irfan Bukhari1, Najma Arshad2, Amjad Hussain1, Nasir Abbas1, Sohail Arshad3, Sajida Parveen1, Naureen Shehzadi1, Shaista Qamar4, and Abida Qamar1 1Punjab University College of Pharmacy, University of the Punjab, Lahore, Pakistan 2Institute of Molecular Biology and Biotechnology, Centre for Research in Molecular Medicine, University of Lahore, Lahore, Pakistan 3Faculty of Pharmacy, Baha Uddin Zakariya University, Multan, Pakistan 4Institute of Pharmaceutical Sciences, University of Veterinary and Animal Sciences, Lahore, Pakistan Abstract Bergenia ciliata (Family: Saxifragaceae) is a folklore remedy for the treatment of various ailments in Asian countries. Bergenin (1) has been isolated as an active constituent in many studies, however, the amount of bergenin has not been determined in all parts of the plant. A simple RP-HPLC method was developed to determine the amount of bergenin in methanol extracts of leaves, rhizomes and roots of the plant. Separation was achieved on an Agilent Eclipse XDB-C18 column maintained at 25 oC using isocratic solvent system (water: methanol: acetic acid; 62.5:37:0.5 v/v/v) adjusted at pH 2 0 at a flow rate of 1.0 mL/min. and detected at 275 nm. Correlation coefficient (0.9952) showed linearity of concentration (5-200 μg/mL) and response. The values of LOD (0.00947 μg/mL) and LOQ (0.02869 μg/mL) indicated that method was sensitive. The recovery of bergenin was 99.99-100% indicating accuracy of method. -
PHYLOGENETIC RELATIONSHIPS of TORREYA (TAXACEAE) INFERRED from SEQUENCES of NUCLEAR RIBOSOMAL DNA ITS REGION Author(S): Jianhua Li, Charles C
PHYLOGENETIC RELATIONSHIPS OF TORREYA (TAXACEAE) INFERRED FROM SEQUENCES OF NUCLEAR RIBOSOMAL DNA ITS REGION Author(s): Jianhua Li, Charles C. Davis, Michael J. Donoghue, Susan Kelley and Peter Del Tredici Source: Harvard Papers in Botany, Vol. 6, No. 1 (July 2001), pp. 275-281 Published by: Harvard University Herbaria Stable URL: http://www.jstor.org/stable/41761652 Accessed: 14-06-2016 15:35 UTC REFERENCES Linked references are available on JSTOR for this article: http://www.jstor.org/stable/41761652?seq=1&cid=pdf-reference#references_tab_contents You may need to log in to JSTOR to access the linked references. Your use of the JSTOR archive indicates your acceptance of the Terms & Conditions of Use, available at http://about.jstor.org/terms JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact [email protected]. Harvard University Herbaria is collaborating with JSTOR to digitize, preserve and extend access to Harvard Papers in Botany This content downloaded from 128.103.224.4 on Tue, 14 Jun 2016 15:35:14 UTC All use subject to http://about.jstor.org/terms PHYLOGENETIC RELATIONSHIPS OF TORREYA (TAXACEAE) INFERRED FROM SEQUENCES OF NUCLEAR RIBOSOMAL DNA ITS REGION Jianhua Li,1 Charles C. Davis,2 Michael J. Donoghue,3 Susan Kelley,1 And Peter Del Tredici1 Abstract. Torreya, composed of five to seven species, is distributed disjunctly in eastern Asia and the eastern and western United States. -
Alligatorweed Scientific Name: Alternanthera Philoxeroides Order
Common Name: Alligatorweed Scientific Name: Alternanthera philoxeroides Order: Caryophyllales Family: Amaranthaceae Wetland Plant Status: Obligatory Ecology & Description The stems of alligatorweed are long (up to 4 ft), hollow, and branched to allow the plant to float. The leaves are opposite, elongated, and elliptical with smooth edges. Leaves have a defined midrib with small pinnate veins. The plant produces a small cluster of white flowers during the warm parts of the year. The flowers are fragrant and consist of 6-10 florets and produce one small seed. Habitat The plant roots in shallow water (less than 6 ½ ft) and then begins to grow out from the anchor. This can be problematic as it can choke off entire waterways. The plant grows in segments and can grow roots or stems out of the nodes that separate each segmented piece. Distribution In the United States, alligatorweed is found from the southern marshes of Virginia to southern Florida and westward to Texas and is found in some parts of California. Native/Invasive Status Alligatorweed is a perennial non-native species of plant from South America that was accidentally introduced in the state of Florida. It is considered invasive in the United States, New Zealand, China, Australia, and Thailand. Alligatorweed is also considered to be a noxious plant because it disrupts water flow and aeration when it becomes thick. In times of high rain fall it can lead to flooding due to its clogging of the waterways. Wildlife Uses Mats of alligatorweed can be good habitat for many aquatic invertebrates and small fish that may serve as a food source for wildlife.