Northern Willowherb Control in Nursery Containers James Altland
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WRITTEN FINDINGS of the WASHINGTON STATE NOXIOUS WEED CONTROL BOARD 2018 Noxious Weed List Proposal
DRAFT: WRITTEN FINDINGS OF THE WASHINGTON STATE NOXIOUS WEED CONTROL BOARD 2018 Noxious Weed List Proposal Scientific Name: Tussilago farfara L. Synonyms: Cineraria farfara Bernh., Farfara radiata Gilib., Tussilago alpestris Hegetschw., Tussilago umbertina Borbás Common Name: European coltsfoot, coltsfoot, bullsfoot, coughwort, butterbur, horsehoof, foalswort, fieldhove, English tobacco, hallfoot Family: Asteraceae Legal Status: Proposed as a Class B noxious weed for 2018, to be designated for control throughout Washington, except for in Grant, Lincoln, Adams, Benton, and Franklin counties. Images: left, blooming flowerheads of Tussilago farfara, image by Caleb Slemmons, National Ecological Observatory Network, Bugwood.org; center, leaves of T. farfara growing with ferns, grasses and other groundcover species; right, mature seedheads of T. farfara before seeds have been dispersed, center and right images by Leslie J. Mehrhoff, University of Connecticut, Bugwood.org. Description and Variation: The common name of Tussilago farfara, coltsfoot, refers to the outline of the basal leaf being that of a colt’s footprint. Overall habit: Tussilago farfara is a rhizomatous perennial, growing up to 19.7 inches (50 cm tall), which can form extensive colonies. Plants first send up flowering stems in the spring, each with a single yellow flowerhead. Just before or after flowers have formed seeds, basal leaves on long petioles grow from the rhizomes, with somewhat roundish leaf blades that are more or less white-woolly on the undersides. Roots: Plants have long creeping, white scaly rhizomes (Griffiths 1994, Chen and Nordenstam 2011). Rhizomes are branching and have fibrous roots (Barkley 2006). They are also brittle and can break easily (Pfeiffer et al. -
Appendix C. Plant Species Observed at the Yolo Grasslands Regional Park (2009-2010)
Appendix C. Plant Species Observed at the Yolo Grasslands Regional Park (2009-2010) Plant Species Observed at the Yolo Grassland Regional Park (2009-2010) Wetland Growth Indicator Scientific Name Common Name Habitat Occurrence Habit Status Family Achyrachaena mollis Blow wives AG, VP, VS AH FAC* Asteraceae Aegilops cylinricia* Jointed goatgrass AG AG NL Poaceae Aegilops triuncialis* Barbed goat grass AG AG NL Poaceae Aesculus californica California buckeye D T NL Hippocastanaceae Aira caryophyllea * [Aspris c.] Silver hairgrass AG AG NL Poaceae Alchemilla arvensis Lady's mantle AG AH NL Rosaceae Alopecurus saccatus Pacific foxtail VP, SW AG OBL Poaceae Amaranthus albus * Pigweed amaranth AG, D AH FACU Amaranthaceae Amsinckia menziesii var. intermedia [A. i.] Rancher's fire AG AH NL Boraginaceae Amsinckia menziesii var. menziesii Common fiddleneck AG AH NL Boraginaceae Amsinckia sp. Fiddleneck AG, D AH NL Boraginaceae Anagallis arvensis * Scarlet pimpernel SW, D, SS AH FAC Primulaceae Anthemis cotula * Mayweed AG AH FACU Asteraceae Anthoxanthum odoratum ssp. odoratum * Sweet vernal grass AG PG FACU Poaceae Aphanes occidentalis [Alchemilla occidentalis] Dew-cup AG, F AH NL Rosaceae Asclepias fascicularis Narrow-leaved milkweed AG PH FAC Ascepiadaceae Atriplex sp. Saltbush VP, SW AH ? Chenopodiaceae Avena barbata * Slender wild oat AG AG NL Poaceae Avena fatua * [A. f. var. glabrata, A. f. var. vilis] Wild oat AG AG NL Poaceae Brassica nigra * Black mustard AG, D AH NL Brassicaceae Brassica rapa field mustard AG, D AH NL Brassicaceae Briza minor * Little quakinggrass AG, SW, SS, VP AG FACW Poaceae Brodiaea californica California brodiaea AG PH NL Amaryllidaceae Brodiaea coronaria ssp. coronaria [B. -
Vestured Pits in Wood of Onagraceae: Correlations with Ecology, Habit, and Phylogeny1
VESTURED PITS IN WOOD OF Sherwin Carlquist2 and Peter H. Raven3 ONAGRACEAE: CORRELATIONS WITH ECOLOGY, HABIT, AND PHYLOGENY1 ABSTRACT All Onagraceae for which data are available have vestured pits on vessel-to-vessel pit pairs. Vestures may also be present in some species on the vessel side of vessel-to-ray pit pairs. Herbaceous Onagraceae do not have fewer vestures, although woods with lower density (Circaea L. and Oenothera L.) have fewer vestures. Some Onagraceae from drier areas tend to have smaller vessel pits, and on that account may have fewer vestures (Epilobium L. and Megacorax S. Gonz´alez & W. L. Wagner). Pit apertures as seen on the lumen side of vessel walls are elliptical, occasionally oval, throughout the family. Vestures are predominantly attached to pit aperture margins. As seen from the outer surfaces of vessels, vestures may extend across the pit cavities. Vestures are usually absent or smaller on the distal portions of pit borders (except for Ludwigia L., which grows consistently in wet areas). Distinctive vesture patterns were observed in the several species of Lopezia Cav. and in Xylonagra Donn. Sm. & Rose. Vestures spread onto the lumen-facing vessel walls of Ludwigia octovalvis (Jacq.) P. H. Raven. Although the genera are presented here in the sequence of a recent molecular phylogeny of Onagraceae, ecology and growth forms are more important than evolutionary relationships with respect to abundance, degree of grouping, and morphology of vestured pits. Designation of vesture types is not warranted based on the distribution of named types in Onagraceae and descriptive adjectives seem more useful, although more data on vesturing in the family are needed before patterns of diversity and their extent can be fully ascertained. -
MONITORING REPORT 2020 BILL BUDD It Is with Great Sadness That We Must Report the Death of Bull Budd in Autumn 2020
Wimbledon and Putney Commons ECOLOGICAL AND ENVIRONMENTAL MONITORING REPORT 2020 BILL BUDD It is with great sadness that we must report the death of Bull Budd in autumn 2020. Bill was our much respected, dragonfly and damselfly recorder and a member of the Wildlife and Conservation Forum. As well as recording on the Commons, Bill also worked as a volunteer at the London Natural History Museum for many years and was the Surrey Vice County Dragonfly Recorder. Bill supported our BioBlitz activities and, with others from the Forum, led dedicated walks raising public awareness of the dragonfly and damselfly populations on the Commons. In September 2020 in recognition of his outstanding contributions to the recording and conservation of Odonata, a newly identified dragonfly species found in the Bornean rainforest* was named Megalogomphus buddi. His contributions will be very much missed. * For further information see: https://british-dragonflies.org.uk/dragonfly-named-after-bds-county-dragonfly-recorder-bill-budd/ Dow, R.A. and Price, B.W. (2020) A review of Megalogomphus sumatranus (Krüger, 1899) and its allies in Sundaland with a description of a new species from Borneo (Odonata: Anisoptera: Gomphidae). Zootaxa 4845 (4): 487–508. https://www.mapress.com/j/zt/article/view/zootaxa.4845.4.2 Accessed 24.02.2021 Thanks are due to everyone who has contributed records and photographs for this report; to the willing volunteers; for the support of Wildlife and Conservation Forum members; and for the reciprocal enthusiasm of Wimbledon and Putney Commons’ staff. A special thank you goes to Angela Evans-Hill for her help with proof reading, chasing missing data and assistance with the final formatting, compilation and printing of this report. -
Diversification in the Microlepidopteran Genus Mompha (Lepidoptera: Gelechioidea
bioRxiv preprint doi: https://doi.org/10.1101/466052; this version posted November 8, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. 1 Diversification in the microlepidopteran genus Mompha (Lepidoptera: Gelechioidea: 2 Momphidae) is explained more by tissue specificity than host plant family. 3 4 5 Authors: Daniel J. Bruzzese1,2,#b,*, David L. Wagner3, Terry Harrison4, Tania Jogesh2, Rick P. 6 Overson2, 5, Norman J. Wickett1,2, Robert A. Raguso6, and Krissa A. Skogen1,2 7 8 9 10 1 Department of Plant Biology and Conservation, Northwestern University, Evanston, IL, USA. 11 2 Division of Plant Science and Conservation, Chicago Botanic Garden, Glencoe, IL, USA. 12 3 Department of Ecology and Evolutionary Biology, University of Connecticut, Storrs, CT, USA. 13 4 345 N. 7th St., Charleston, IL USA. 14 5 Global Institute of Sustainability, Arizona State University, Tempe, AZ, USA. 15 6 Department of Neurobiology and Behavior, Cornell University, Ithaca, NY, USA. 16 #b Current Address: Department of Biological Sciences, University of Notre Dame, South Bend, 17 IN, USA. 18 19 20 *Corresponding author 21 E-mail: [email protected] (DJB) 22 23 24 1 bioRxiv preprint doi: https://doi.org/10.1101/466052; this version posted November 8, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. -
Skokholm Annual Report 2017
Wardens’ Report iii Introduction to the Skokholm Island Annual Report 2017 iii The 2017 Season and Weather Summary v Spring Work Parties vii Spring Long-term Volunteers viii Spring Migration Highlights viii The Breeding Season x Autumn Migration Highlights xi Autumn Long-term Volunteers xii Autumn Work Party xii Skokholm Bird Observatory xiii Digitisation of the Paper Logs xiii Ringing Projects xiii Visiting Ringers xiv Birds Ringed in 2017 xv Catching Methods xv Arrival and Departure Dates xvii 2016 Rarity Decisions and DNA Results xvii Bird Observatory Fundraising xviii Acknowledgments and Thanks xviii Definitions and Terminology 1 The Systematic List of Birds 1 Anatidae Geese and Ducks 1 Phasianidae Quail 7 Gaviidae Divers 7 Hydrobatidae Storm Petrel 7 Procellariidae Fulmar and Shearwaters 17 Podicipedidae Grebes 31 Threskiornithidae Spoonbill 31 Ardeidae Bittern, Grey Heron and Egrets 32 Sulidae Gannet 33 Phalacrocoracidae Shag and Cormorant 34 Accipitridae Hawks, Hen Harrier, Red Kite & Buzzard 36 Rallidae Water Rail, Moorhen and Coot 39 Gruidae Crane 41 Haematopodidae Oystercatcher 42 Recurvirostridae Avocet 43 Charadriidae Plovers 44 Scolopacidae Sandpipers and allies 45 Laridae Gulls 57 Sternidae Terns 75 Stercorariidae Skuas 76 Alcidae Auks 77 Columbidae Pigeons and Doves 94 Cuculidae Cuckoo 95 Strigidae Short-eared Owl 96 Apodidae Swift 97 Upupidae Hoopoe 97 Picidae Wryneck 98 Falconidae Kestrel, Merlin and Peregrine 98 Corvidae Crows 100 ii | Skokholm Annual Report 2017 Paridae Blue Tit 106 Alaudidae Skylark 107 Hirundinidae -
Plants and Plant Parts
BVL-Report · 8.8 List of Substances of the Competent Federal Government and Federal State Authorities Category “Plants and plant parts” List of Substances of the Competent Federal Government and Federal State Authorities Category “Plants and plant parts” List of Substances of the Competent Federal Government and Federal State Authorities Category “Plants and plant parts” BVL-Reporte IMPRINT ISBN 978-3-319-10731-8 ISBN 978-3-319-10732-5 (eBook) DOI 10.1007/978-3-319-10732-5 Springer Cham Heidelberg New York Dordrecht London This work is subject to copyright. All rights are reserved, whether the whole or part of the material is concerned, specifically the rights of translation, reprinting, reuse of illustrations, recitation, broad- casting, reproduction on microfilm or in any other way, and storage in data banks. Duplication of this publication or parts thereof is permitted only under the provisions of the German Copyright Law of September 9, 1965, in its current version, and permission for use must always be obtained from Springer. Violations are liable to prosecution under the German Copyright Law. The use of general descriptive names, registered names, trademarks, etc. in this publication does not imply, even in the absence of a specific statement, that such names are exempt from the relevant protective laws and regulations and therefore free for general use. While the advice and information in this book are believed to be true and accurate at the date of publication, neither the authors nor the editors nor the publisher can accept any legal responsibility for any errors or omissions that may be made. -
Royal Military Canal Management Plan 2021 - 2025 1
Folkestone & Hythe District Council Royal Military Canal Management Plan 2021 – 2025 Folkestone & Hythe District Council Royal Military Canal Management Plan 2021 - 2025 1 Contents 1 Introduction 4 2 Site Details 5 2.1 Population Distribution 5 2.2 Diverse Countryside 5 2.3 Transport Links 5 2.4 Directions 6 2.5 Site Description 6 2.6 Public Rights of Way Map 8 3 Site History 9 4 Maintenance Plan 10 4.1 Grounds Maintenance Maps 11 4.2 Grounds Maintenance Specification Table 17 4.3 Water Management 19 4.4 Interpretation and Signage 20 4.5 Seabrook Play Area 21 4.6 Management Action Plan 22 5 Health and Safety 30 5.1 Introduction 30 5.2 Security 30 5.3 Equipment and Facilities 31 5.4 Chemical Use 31 5.5 Vehicles and Machinery 31 5.6 Personal Protective Equipment and Signage 32 6 Facilities 33 6.1 Boat Hire 33 6.2 Canoeing and Boating 33 6.3 Seabrook Play Area 34 6.4 Fishing 35 6.5 Public Rights of Way 35 6.6 Picnic Sites 36 6.7 Nearby Facilities 37 7 Nature Conservation and Heritage 38 7.1 Nature Conservation 38 7.2 Habitat Management 42 7.3 Tree Management 42 7.4 Heritage 43 8 Sustainability 45 8.1 Biodiversity 45 8.2 Green Waste and Composting 45 8.3 Peat 46 8.4 Waste Management 46 8.5 Tree Stock 46 Folkestone & Hythe District Council Royal Military Canal Management Plan 2021 - 2025 2 8.6 Grass Cutting 46 8.7 Furniture and Equipment 46 8.8 Chemical Use 47 8.9 Vehicles and Machinery 48 8.10 Recycling 49 8.11 Horticulture 49 9 Marketing 50 9.1 Leaflet and Self-guided Walks 50 9.2 Events 50 9.3 Interpretation and Signage 50 9.4 Social Media and Web Advertising 51 10 Community Involvement 52 10.1 Events 52 10.2 Community Groups 52 10.3 Volunteers 53 11 Species Lists 2010-2020 collected by local enthusiasts 55 12 List of Appendices 72 Folkestone & Hythe District Council Royal Military Canal Management Plan 2021 - 2025 3 Introduction The Royal Military Canal (RMC) was constructed between 1804 and 1809 as a defensive structure against Napoleonic invasion. -
Fireweed (Epilobium Angustifolium L.): Botany, Phytochemistry and Traditional Uses
DOI: 10.2478/hepo-2018-000 International journal edited by the Institute of Natural Fibres and Medicinal Plants Vol. 65 No. 3 2019 Received: 2019-08-01 DOI: 10.2478/hepo-2019-0018 DOI: 10.2478/hepo-2018-000 Accepted: 2019-09-20 Available online: 2019-09-30 REVIEW PAPER Fireweed (Epilobium angustifolium L.): botany, phytochemistry and traditional uses. A review ARTUR ADAMCZAK1*, MARIOLA DREGER2, KATARZYNA SEIDLER-ŁOŻYKOWSKA1, KAROLINA WIELGUS2 1Department of Botany, Breeding and Agricultural Technology of Medicinal Plants Institute of Natural Fibres and Medicinal Plants Kolejowa 2 62-064 Plewiska, Poland 2Department of Biotechnology Institute of Natural Fibres and Medicinal Plants Wojska Polskiego 71B 60-630 Poznań, Poland *corresponding author: phone: +48 (61) 665-95-50, e-mail: [email protected] Summary Fireweed (Epilobium angustifolium L., Onagraceae) is one of important medicinal plants used especially in the treatment of urogenital disorders, including benign prostatic hyperplasia (BPH) and prostatitis. The therapeutic effects of E. angustifolium extracts comprise antiproliferative, anti-inflammatory, immunomod- ulatory, antioxidant, and also antimicrobial activities. The aim of the present review was to provide the in- formation on the botany, phytochemistry and traditional uses of E. angustifolium. This plant is a widespread circumboreal species of North America and Eurasia, tolerant in terms of habitat conditions, and often oc- cupying man-made open habitats. Phytochemical studies on E. angustifolium resulted in the identification of about 250 different metabolites, including about 170 substances found for the first time in this plant in the last six years (2014–2019). Fireweed has an abundance of polyphenolic compounds, particularly ellagi- tannins. -
Flora of China 13: 409–411. 2007. 3. CHAMERION (Rafinesque
Flora of China 13: 409–411. 2007. 3. CHAMERION (Rafinesque) Rafinesque ex Holub, Folia Geobot. Phytotax. 7: 85. 1972. 柳兰属 liu lan shu Chen Jiarui (陈家瑞 Chen Chia-jui); Peter C. Hoch, Peter H. Raven Epilobium subg. Chamerion Rafinesque, Amer. Monthly Mag. & Crit. Rev. 2: 266. 1818. Herbs perennial, erect, usually clumped, with shoots from woody caudex or spreading lateral roots. Stems simple or rarely branched, pubescent to subglabrous, hairs always eglandular. Leaves spirally arranged, rarely subopposite or subverticillate, sublea- thery, basal ones sessile, upper ones usually petiolate; stipules absent; bracteoles absent. Inflorescence a simple raceme or spike, rarely branched. Flowers 4-merous, slightly zygomorphic, strongly protandrous, lacking a floral tube, producing nectar from raised disk at base of style and stamens. Petals pink to rose-purple, rarely white, obcordate or obtrullate, entire. Stamens 8, subequal in single whorl, erect at onset of anthesis, later reflexed; pollen blue or yellow, shed in monads. Style initially deflexed, becoming erect as stigma deflexes; stigma deeply 4-lobed and revolute, receptive on inner surfaces. Fruit an elongate capsule, slender, 4-loculed, loculidical. Seeds many, with terminal coma of silky hairs. 2n = 36, 72, 108. Eight species: montane to arctic N hemisphere, widespread in Asia and Europe, barely reaching N Africa, and in North America south to the high mountains of C Mexico; four species in China. The species occur primarily in moist, rocky areas in high-montane regions, with one species (Chamerion angustifolium) more widespread in dis- turbed, temperate habitats. Raven (Ann. Missouri Bot. Gard. 63: 326–340. 1977 [“1976”]) divided this group into two subsections under Epilobium sect. -
Macro-Moths As Possible Assessment Endpoints for Non-Target Effects of Bt-Maize Pollen: a Faunistic Study in Three Italian Protected Areas
Bulletin of Insectology 70 (2): 307-314, 2017 ISSN 1721-8861 Macro-moths as possible assessment endpoints for non-target effects of Bt-maize pollen: a faunistic study in three Italian protected areas 1 2 3 1 2 Antonio MASETTI , Salvatore ARPAIA , Silvia GHESINI , Serena MAGAGNOLI , Ferdinando BALDACCHINO , 2 4 5 5 Rosaria Alessandra MAGARELLI , Ulderico NERI , Matteo LENER , Valentina RASTELLI , Giovanni 5 6 3 1 STAIANO , Andreas LANG , Mario MARINI , Giovanni BURGIO 1Dipartimento di Scienze Agrarie - Entomologia, Università di Bologna, Italy 2ENEA, Agenzia Nazionale per le Nuove Tecnologie, l’Energia e lo Sviluppo Economico Sostenibile, Centro Ricer- che Trisaia, Rotondella, Matera, Italy 3Dipartimento di Scienze Biologiche, Geologiche e Ambientali, Università di Bologna, Italy 4Consiglio per la ricerca in agricoltura e l’analisi dell’economia agraria - Centro di ricerca per lo studio delle re- lazioni tra pianta e suolo - (CREA-RPS), Rome, Italy 5Istituto Superiore per la Protezione e la Ricerca Ambientale, Rome, Italy 6Environmental Geosciences, University of Basel, Switzerland Abstract Lepidoptera are the phytophagous group most at risk of impact by insect-resistant genetically modified (GM) plants since most of these crops have been developed to express toxins to specifically target lepidopteran pests. In the case of Bt-maize cultivation, pollen grains released by GM plants could dust larval host plants growing inside or nearby maize fields, thus leading to the expo- sure of caterpillars to the Cry toxins. This way of exposure has been studied mainly for butterflies, whereas moths, in spite of their great diversity and abundance, were rarely considered. To evaluate the potential exposure of moth species to maize pollen in ab- sence of Cry-expressing plants, macro-moths were sampled by means of light traps in three protected areas of Northern, Central and Southern Italy where conventional maize is among the main crops. -
Plant Invaders of Mid-Atlantic Natural Areas Revised & Updated – with More Species and Expanded Control Guidance
Plant Invaders of Mid-Atlantic Natural Areas Revised & Updated – with More Species and Expanded Control Guidance National Park Service U.S. Fish and Wildlife Service 1 I N C H E S 2 Plant Invaders of Mid-Atlantic Natural Areas, 4th ed. Authors Jil Swearingen National Park Service National Capital Region Center for Urban Ecology 4598 MacArthur Blvd., N.W. Washington, DC 20007 Britt Slattery, Kathryn Reshetiloff and Susan Zwicker U.S. Fish and Wildlife Service Chesapeake Bay Field Office 177 Admiral Cochrane Dr. Annapolis, MD 21401 Citation Swearingen, J., B. Slattery, K. Reshetiloff, and S. Zwicker. 2010. Plant Invaders of Mid-Atlantic Natural Areas, 4th ed. National Park Service and U.S. Fish and Wildlife Service. Washington, DC. 168pp. 1st edition, 2002 2nd edition, 2004 3rd edition, 2006 4th edition, 2010 1 Acknowledgements Graphic Design and Layout Olivia Kwong, Plant Conservation Alliance & Center for Plant Conservation, Washington, DC Laurie Hewitt, U.S. Fish & Wildlife Service, Chesapeake Bay Field Office, Annapolis, MD Acknowledgements Funding provided by the National Fish and Wildlife Foundation with matching contributions by: Chesapeake Bay Foundation Chesapeake Bay Trust City of Bowie, Maryland Maryland Department of Natural Resources Mid-Atlantic Invasive Plant Council National Capital Area Garden Clubs Plant Conservation Alliance The Nature Conservancy, Maryland–DC Chapter Worcester County, Maryland, Department of Comprehensive Planning Additional Fact Sheet Contributors Laurie Anne Albrecht (jetbead) Peter Bergstrom (European