Rytidosperma Popinensis (Blue Wallabygrass) Rytidosperma Popinensis
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Seed Ecology Iii
SEED ECOLOGY III The Third International Society for Seed Science Meeting on Seeds and the Environment “Seeds and Change” Conference Proceedings June 20 to June 24, 2010 Salt Lake City, Utah, USA Editors: R. Pendleton, S. Meyer, B. Schultz Proceedings of the Seed Ecology III Conference Preface Extended abstracts included in this proceedings will be made available online. Enquiries and requests for hardcopies of this volume should be sent to: Dr. Rosemary Pendleton USFS Rocky Mountain Research Station Albuquerque Forestry Sciences Laboratory 333 Broadway SE Suite 115 Albuquerque, New Mexico, USA 87102-3497 The extended abstracts in this proceedings were edited for clarity. Seed Ecology III logo designed by Bitsy Schultz. i June 2010, Salt Lake City, Utah Proceedings of the Seed Ecology III Conference Table of Contents Germination Ecology of Dry Sandy Grassland Species along a pH-Gradient Simulated by Different Aluminium Concentrations.....................................................................................................................1 M Abedi, M Bartelheimer, Ralph Krall and Peter Poschlod Induction and Release of Secondary Dormancy under Field Conditions in Bromus tectorum.......................2 PS Allen, SE Meyer, and K Foote Seedling Production for Purposes of Biodiversity Restoration in the Brazilian Cerrado Region Can Be Greatly Enhanced by Seed Pretreatments Derived from Seed Technology......................................................4 S Anese, GCM Soares, ACB Matos, DAB Pinto, EAA da Silva, and HWM Hilhorst -
Species of the Box-Gum Woodlands and Derived Native Grasslands
White Box-Yellow Box-Blakely’s Red Gum Grassy Woodland and Derived Native Grassland Ecological Community Species List White Box-Yellow Box-Blakely’s Red Gum Grassy Woodland and Derived Native Grassland Ecological Community Species List This species list is designed to provide information about plant species that can be found in the White Box-Yellow Box-Blakely’s Red Gum Grassy Woodland and Derived Native Grassland ecological community listed under the Environment Protection and Biodiversity Conservation Act 1999. The species list was developed to complement the Listing Information Guide, and should be read in that context. It provides information on scientific and common names of the species, the kind of plant the species is, whether it is an ‘important’ species for the purposes of this ecological community and whether it is exotic or native, perennial or annual. The list is not exhaustive and not all of the species listed will occur in every patch of White Box-Yellow Box-Blakely’s Red Gum Grassy Woodland and Derived Native Grassland. If there are any species that you think should be added to the list, removed from the list, or that are categorised incorrectly, please contact [email protected]. As such, this document may change over time and you should check that you are referring to the most recent version of the list. Caveat: This list has been compiled from a range of sources. While reasonable efforts have been made to ensure the accuracy of the information, no guarantee is given, nor responsibility taken, by the Commonwealth for its accuracy, currency or completeness. -
Full Article
Volume 3(4): 599 TELOPEA Publication Date: 12 April 1990 Til. Ro)'al BOTANIC GARDENS dx.doi.org/10.7751/telopea19904909 Journal of Plant Systematics 6 DOPII(liPi Tm st plantnet.rbgsyd.nsw.gov.au/Telopea • escholarship.usyd.edu.au/journals/index.php/TEL· ISSN 0312-9764 (Print) • ISSN 2200-4025 (Online) Telopea Vol. 3(4): 599 (1990) 599 SHORT COMMUNICATION Amphibromus nervosus (Poaceae), an earlier combination and further synonyms Arthur Chapman, Bureau of Flora & Fauna, Canberra, has kindly pointed out to me that the combination Amphibromus nervosus (J. D. Hook.) Baillon had been made in 1893, earlier than the combination made by G. C. Druce re ported in our revision of the genus Amphibromus in Australia (Jacobs and Lapinpuro 1986). Baillon's combination had been overlooked by Index Kewensis and by the Chase Index (Chase and Niles 1962). The full citation is: Amphibromus nervosus (J. D. Hook.) Baillon, Histoire des Plantes 12: 203 (1893). BASIONYM: Danthonia nervosa J. D. Hook., Fl.FI. Tasm. 2: 121, pI.pl. 163A (1858). Hooker based his combination on the illegitimate Avena nervosa R. Br. (see Jacobs and Lapinpuro 1986 for further comment). Amphibromus nervosus (1. D. Hook.) G. C. Druce then becomes a superfluous combina tion and is added to the synonymy. Arthur Chapman also kindly pointed out a synonym that to the best of my knowledge has not been used beyond its initial publication. This synonym is: Avenastrum nervosum Vierh., Verhandlungen der Gesellschaft Deutscher Naturforscher und Artze 85. Versammlung zu Wien (Leipzig) 1: 672 (1913). This name was based on the illegitimate Avena nervosa R. -
Phylogeny and Subfamilial Classification of the Grasses (Poaceae) Author(S): Grass Phylogeny Working Group, Nigel P
Phylogeny and Subfamilial Classification of the Grasses (Poaceae) Author(s): Grass Phylogeny Working Group, Nigel P. Barker, Lynn G. Clark, Jerrold I. Davis, Melvin R. Duvall, Gerald F. Guala, Catherine Hsiao, Elizabeth A. Kellogg, H. Peter Linder Source: Annals of the Missouri Botanical Garden, Vol. 88, No. 3 (Summer, 2001), pp. 373-457 Published by: Missouri Botanical Garden Press Stable URL: http://www.jstor.org/stable/3298585 Accessed: 06/10/2008 11:05 Your use of the JSTOR archive indicates your acceptance of JSTOR's Terms and Conditions of Use, available at http://www.jstor.org/page/info/about/policies/terms.jsp. JSTOR's Terms and Conditions of Use provides, in part, that unless you have obtained prior permission, you may not download an entire issue of a journal or multiple copies of articles, and you may use content in the JSTOR archive only for your personal, non-commercial use. Please contact the publisher regarding any further use of this work. Publisher contact information may be obtained at http://www.jstor.org/action/showPublisher?publisherCode=mobot. Each copy of any part of a JSTOR transmission must contain the same copyright notice that appears on the screen or printed page of such transmission. JSTOR is a not-for-profit organization founded in 1995 to build trusted digital archives for scholarship. We work with the scholarly community to preserve their work and the materials they rely upon, and to build a common research platform that promotes the discovery and use of these resources. For more information about JSTOR, please contact [email protected]. -
Edible Seeds and Grains of California Tribes
National Plant Data Team August 2012 Edible Seeds and Grains of California Tribes and the Klamath Tribe of Oregon in the Phoebe Apperson Hearst Museum of Anthropology Collections, University of California, Berkeley August 2012 Cover photos: Left: Maidu woman harvesting tarweed seeds. Courtesy, The Field Museum, CSA1835 Right: Thick patch of elegant madia (Madia elegans) in a blue oak woodland in the Sierra foothills The U.S. Department of Agriculture (USDA) prohibits discrimination in all its pro- grams and activities on the basis of race, color, national origin, age, disability, and where applicable, sex, marital status, familial status, parental status, religion, sex- ual orientation, genetic information, political beliefs, reprisal, or because all or a part of an individual’s income is derived from any public assistance program. (Not all prohibited bases apply to all programs.) Persons with disabilities who require alternative means for communication of program information (Braille, large print, audiotape, etc.) should contact USDA’s TARGET Center at (202) 720-2600 (voice and TDD). To file a complaint of discrimination, write to USDA, Director, Office of Civil Rights, 1400 Independence Avenue, SW., Washington, DC 20250–9410, or call (800) 795-3272 (voice) or (202) 720-6382 (TDD). USDA is an equal opportunity provider and employer. Acknowledgments This report was authored by M. Kat Anderson, ethnoecologist, U.S. Department of Agriculture, Natural Resources Conservation Service (NRCS) and Jim Effenberger, Don Joley, and Deborah J. Lionakis Meyer, senior seed bota- nists, California Department of Food and Agriculture Plant Pest Diagnostics Center. Special thanks to the Phoebe Apperson Hearst Museum staff, especially Joan Knudsen, Natasha Johnson, Ira Jacknis, and Thusa Chu for approving the project, helping to locate catalogue cards, and lending us seed samples from their collections. -
Ecological Ranges of Plant Species in the Monsoon Zone of the Russian Far East
In: Horizons in Earth Science Research, Volume 3 ISBN: 978-1-61122-197-8 Editors: Benjamin Veress and Jozsi Szigethy © 2011 Nova Science Publishers, Inc. The exclusive license for this PDF is limited to personal website use only. No part of this digital document may be reproduced, stored in a retrieval system or transmitted commercially in any form or by any means. The publisher has taken reasonable care in the preparation of this digital document, but makes no expressed or implied warranty of any kind and assumes no responsibility for any errors or omissions. No liability is assumed for incidental or consequential damages in connection with or arising out of information contained herein. This digital document is sold with the clear understanding that the publisher is not engaged in rendering legal, medical or any other professional services. Chapter 2 ECOLOGICAL RANGES OF PLANT SPECIES IN THE MONSOON ZONE OF THE RUSSIAN FAR EAST Vitaly P. Seledets1* and Nina S. Probatova2 1Pacific Institute of Geography FEB RAS, 690041 Vladivostok, Russia 2Institute of Biology and Soil Science FEB RAS, 690022 Vladivostok, Russia ABSTRACT The monsoon zone covers a considerable part of the Russian Far East (RFE), which includes the Kamchatka Peninsula, Sakhalin, the Kurile Islands, the continental coasts and islands of the Bering Sea, the Sea of Okhotsk, the Sea of Japan, and the Amur River basin. The problem of biodiversity in the monsoon zone is connected to species adaptations, speciation and florogenesis, the formation of plant communities, vegetation dynamics, and population structure. Our concept of the ecological range (ecorange, ER) of plant species (Seledets & Probatova 2007b) is aimed at adaptive strategies in the RFE monsoon zone compared with Inner Asia. -
Mitteilungen Der Botanischen Staatssammlung München
© Biodiversity Heritage Library, http://www.biodiversitylibrary.org/; www.biologiezentrum.at Mitt. Bot. Staatssamml. München © Biodiversity Heritage Library, http://www.biodiversitylibrary.org/; www.biologiezentrum.at well within their lowermost leaf-sheaths. Besides these characters another can be observed in South American species, namely tufts of hairs in a trans- verse line across the back of the lemma just beneath the Insertion of the cen- tral awn. Species, which exhibit this character, are, however, not confined to South America but occur also in the Easter-Island, in New Zealand, Austra- lia, Tasmania, Indonesia and in the Himalayas. ZoTOV has based his genus Notodanthonia on species from New Zealand. It remains to be decided whether or not this genus should be retained. Only the study of the South American species can elucidate this problem. None of the groups mentioned so far occurs in southern Africa. None- theless, not fewer than 121 Danthonia species have been described from the- re. It goes without saying that many of these names are synonyms. More- over, over the years, quite a number of these species have been separated into different genera which have been recognized by most students of African Gramineae. These include well-known generic names such as Pentameris, Pentaschistis, Strehlochaete, Chaetohromus, Alloeochaete as well as Phacnan- thoecium. But, even so, 36 species remain in Danthonia as can be seen in C. E. Hubbard's treatment of this group in the Flora of Tropical Africa and in Miss Chippindall's cursory guide to South African grasses. In the following account these remaining species of Danthonia will be considered: The first 4 taxa described as Danthonia can be distinguished from typical Danthonia at a first glance by having a long pungent callus at the base of each floret. -
Native Grasses Make New Products – a Review of Current and Past Uses and Assessment of Potential
Native grasses make new products – a review of current and past uses and assessment of potential JUNE 2015 RIRDC Publication No. 15/056 Native grasses make new products A review of current and past uses and assessment of potential by Ian Chivers, Richard Warrick, Janet Bornman and Chris Evans June 2015 RIRDC Publication No 15/056 RIRDC Project No PRJ-009569 © 2015 Rural Industries Research and Development Corporation. All rights reserved. ISBN 978-1-74254-802-9 ISSN 1440-6845 Native grasses make new products: a review of current and past uses and assessment of potential Publication No. 15/056 Project No. PRJ-009569 The information contained in this publication is intended for general use to assist public knowledge and discussion and to help improve the development of sustainable regions. You must not rely on any information contained in this publication without taking specialist advice relevant to your particular circumstances. While reasonable care has been taken in preparing this publication to ensure that information is true and correct, the Commonwealth of Australia gives no assurance as to the accuracy of any information in this publication. The Commonwealth of Australia, the Rural Industries Research and Development Corporation (RIRDC), the authors or contributors expressly disclaim, to the maximum extent permitted by law, all responsibility and liability to any person, arising directly or indirectly from any act or omission, or for any consequences of any such act or omission, made in reliance on the contents of this publication, whether or not caused by any negligence on the part of the Commonwealth of Australia, RIRDC, the authors or contributors. -
REVIEW ARTICLE Fire, Grazing and the Evolution of New Zealand Grasses
AvailableMcGlone on-lineet al.: Evolution at: http://www.newzealandecology.org/nzje/ of New Zealand grasses 1 REVIEW ARTICLE Fire, grazing and the evolution of New Zealand grasses Matt S. McGlone1*, George L. W. Perry2,3, Gary J. Houliston1 and Henry E. Connor4 1Landcare Research, PO Box 69040, Lincoln 7640, New Zealand 2School of Environment, University of Auckland, Private Bag 92019, Auckland 1142, New Zealand 3School of Biological Sciences, University of Auckland, Private Bag 92019, Auckland 1142, New Zealand 4Department of Geography, University of Canterbury, Private Bag 4800, Christchurch 8140, New Zealand *Author for correspondence (Email: [email protected]) Published online: 7 November 2013 Abstract: Less than 4% of the non-bamboo grasses worldwide abscise old leaves, whereas some 18% of New Zealand native grasses do so. Retention of dead or senescing leaves within grass canopies reduces biomass production and encourages fire but also protects against mammalian herbivory. Recently it has been argued that elevated rates of leaf abscission in New Zealand’s native grasses are an evolutionary response to the absence of indigenous herbivorous mammals. That is, grass lineages migrating to New Zealand may have increased biomass production through leaf-shedding without suffering the penalty of increased herbivory. We show here for the Danthonioideae grasses, to which the majority (c. 74%) of New Zealand leaf-abscising species belong, that leaf abscission outside of New Zealand is almost exclusively a feature of taxa of montane and alpine environments. We suggest that the reduced frequency of fire in wet, upland areas is the key factor as montane/alpine regions also experience heavy mammalian grazing. -
Classification of the Vegetation Alliances and Associations of Sonoma County, California
Classification of the Vegetation Alliances and Associations of Sonoma County, California Volume 1 of 2 – Introduction, Methods, and Results Prepared by: California Department of Fish and Wildlife Vegetation Classification and Mapping Program California Native Plant Society Vegetation Program For: The Sonoma County Agricultural Preservation and Open Space District The Sonoma County Water Agency Authors: Anne Klein, Todd Keeler-Wolf, and Julie Evens December 2015 ABSTRACT This report describes 118 alliances and 212 associations that are found in Sonoma County, California, comprising the most comprehensive local vegetation classification to date. The vegetation types were defined using a standardized classification approach consistent with the Survey of California Vegetation (SCV) and the United States National Vegetation Classification (USNVC) system. This floristic classification is the basis for an integrated, countywide vegetation map that the Sonoma County Vegetation Mapping and Lidar Program expects to complete in 2017. Ecologists with the California Department of Fish and Wildlife and the California Native Plant Society analyzed species data from 1149 field surveys collected in Sonoma County between 2001 and 2014. The data include 851 surveys collected in 2013 and 2014 through funding provided specifically for this classification effort. An additional 283 surveys that were conducted in adjacent counties are included in the analysis to provide a broader, regional understanding. A total of 34 tree-overstory, 28 shrubland, and 56 herbaceous alliances are described, with 69 tree-overstory, 51 shrubland, and 92 herbaceous associations. This report is divided into two volumes. Volume 1 (this volume) is composed of the project introduction, methods, and results. It includes a floristic key to all vegetation types, a table showing the full local classification nested within the USNVC hierarchy, and a crosswalk showing the relationship between this and other classification systems. -
Literaturverzeichnis
Literaturverzeichnis Abaimov, A.P., 2010: Geographical Distribution and Ackerly, D.D., 2009: Evolution, origin and age of Genetics of Siberian Larch Species. In Osawa, A., line ages in the Californian and Mediterranean flo- Zyryanova, O.A., Matsuura, Y., Kajimoto, T. & ras. Journal of Biogeography 36, 1221–1233. Wein, R.W. (eds.), Permafrost Ecosystems. Sibe- Acocks, J.P.H., 1988: Veld Types of South Africa. 3rd rian Larch Forests. Ecological Studies 209, 41–58. Edition. Botanical Research Institute, Pretoria, Abbadie, L., Gignoux, J., Le Roux, X. & Lepage, M. 146 pp. (eds.), 2006: Lamto. Structure, Functioning, and Adam, P., 1990: Saltmarsh Ecology. Cambridge Uni- Dynamics of a Savanna Ecosystem. Ecological Stu- versity Press. Cambridge, 461 pp. dies 179, 415 pp. Adam, P., 1994: Australian Rainforests. Oxford Bio- Abbott, R.J. & Brochmann, C., 2003: History and geography Series No. 6 (Oxford University Press), evolution of the arctic flora: in the footsteps of Eric 308 pp. Hultén. Molecular Ecology 12, 299–313. Adam, P., 1994: Saltmarsh and mangrove. In Groves, Abbott, R.J. & Comes, H.P., 2004: Evolution in the R.H. (ed.), Australian Vegetation. 2nd Edition. Arctic: a phylogeographic analysis of the circu- Cambridge University Press, Melbourne, pp. marctic plant Saxifraga oppositifolia (Purple Saxi- 395–435. frage). New Phytologist 161, 211–224. Adame, M.F., Neil, D., Wright, S.F. & Lovelock, C.E., Abbott, R.J., Chapman, H.M., Crawford, R.M.M. & 2010: Sedimentation within and among mangrove Forbes, D.G., 1995: Molecular diversity and deri- forests along a gradient of geomorphological set- vations of populations of Silene acaulis and Saxi- tings. -
INVASIVE SPECIES Grass Family (Poaceae) Wild Oats Are Annuals
A PROJECT OF THE SONOMA-MARIN COASTAL PRAIRIE WORKING GROUP INVASIVE SPECIES I NVASIVE A NNUAL P LANTS WILD OATS (AVENA FATUA) AND SLENDER WILD OATS (AVENA BARBATA) - NON-NATIVE Grass Family (Poaceae) Wild oats are annuals. WILD OATS: Are native to Eurasia and North Africa. WILD OAT ECOLOGY Is often dominant or co-dominant in coastal prairie (Ford and Hayes 2007; Sawyer, et al. 2009), Occurs in moist lowland prairies, drier upland prairies and open woodlands (Darris and Gonzalves 2008), Species Interactions: The success of Avena lies in its superior competitive ability: o It has a dense root system. The total root length of a single Avena plant can be from 54.3 miles long (Pavlychenko 1937) to, most likely, twice that long (Dittmer 1937). Wild oats (Avena) in Marin coastal grassland. o It produces allelopathic compounds, Photo by D. (Immel) Jeffery, 2010. chemicals that inhibit the growth of other adjacent plant species. o It has long-lived seeds that can survive for as long as 10 years in the soil (Whitson 2002). Citation: Jeffery (Immel), D., C. Luke, K. Kraft. Last modified February 2020. California’s Coastal Prairie. A project of the Sonoma Marin Coastal Grasslands Working Group, California. Website: www.cnga.org/prairie. Coastal Prairie Described > Species: Invasives: Page 1 of 18 o Pavlychenko (1937) found that, although Avena is a superior competitor when established, it is relatively slow (as compared to cultivated cereal crops wheat, rye and barley) to develop seminal roots in the early growth stages. MORE FUN FACTS ABOUT WILD OATS Avena is Latin for “oat.” The cultivated oat (Avena sativa), also naturalized in California) is thought to be derived from wild oats (Avena fatua) by early humans (Baum and Smith [2011]).