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African Boxthorn (Lycium Ferocissimum)
Managing weeds for biodiversity ● Recorded distribution African boxthorn (Lycium ferocissimum) The problem the original native vegetation cover has The leaves are generally 10–40 mm been removed, boxthorn’s dense foliage long, 4–10 mm wide, bright green, African boxthorn (commonly known may be used as habitat by native fauna smooth and rather fleshy. They are oval as boxthorn) is a widespread weed in such as fairy wrens and the fruit may in shape with a rounded tip and occur African boxthorn regional Australia. It is considered a be a food source for native animals. in clusters along branchlets and at the major problem because it invades native base of thorns. Many agencies, community groups and vegetation, alters habitat and overruns individuals expend considerable resources Boxthorn mainly flowers in spring and pastures and other areas. It forms dense, each year on planning and undertaking summer but flowers may be present any impenetrable thickets that exclude other boxthorn control. While not among time of year. Flowers hang on stalks, plants, can provide shelter and food the 20 Weeds of National Significance, singly or in pairs. They are white to for feral animals such as foxes, rabbits, ferocissimum – Lycium boxthorn was ranked a close 24th in the mauve with a tubular base, usually five- starlings and sparrows and reduce assessment of Australia’s worst weeds. lobed and about 12 mm in diameter. access for stock, native animals, people However, very little research has been Fruit is a smooth round berry, 5–12 mm and vehicles. Its large thorns can also done on its ecology. -
A Framework for Mapping Vegetation Over Broad Spatial Extents: a Technique to Aid Land Management Across Jurisdictional Boundaries
Landscape and Urban Planning 97 (2010) 296–305 Contents lists available at ScienceDirect Landscape and Urban Planning journal homepage: www.elsevier.com/locate/landurbplan A framework for mapping vegetation over broad spatial extents: A technique to aid land management across jurisdictional boundaries Angie Haslem a,b,∗, Kate E. Callister a, Sarah C. Avitabile a, Peter A. Griffioen c, Luke T. Kelly b, Dale G. Nimmo b, Lisa M. Spence-Bailey a, Rick S. Taylor a, Simon J. Watson b, Lauren Brown a, Andrew F. Bennett b, Michael F. Clarke a a Department of Zoology, La Trobe University, Bundoora, Victoria 3086, Australia b School of Life and Environmental Sciences, Deakin University, Burwood, Victoria 3125, Australia c Peter Griffioen Consulting, Ivanhoe, Victoria 3079, Australia article info abstract Article history: Mismatches in boundaries between natural ecosystems and land governance units often complicate an Received 2 October 2009 ecosystem approach to management and conservation. For example, information used to guide man- Received in revised form 25 June 2010 agement, such as vegetation maps, may not be available or consistent across entire ecosystems. This Accepted 5 July 2010 study was undertaken within a single biogeographic region (the Murray Mallee) spanning three Aus- Available online 7 August 2010 tralian states. Existing vegetation maps could not be used as vegetation classifications differed between states. Our aim was to describe and map ‘tree mallee’ vegetation consistently across a 104 000 km2 area Keywords: of this region. Hierarchical cluster analyses, incorporating floristic data from 713 sites, were employed Semi-arid ecosystems Mallee vegetation to identify distinct vegetation types. Neural network classification models were used to map these veg- Remote sensing etation types across the region, with additional data from 634 validation sites providing a measure of Neural network classification models map accuracy. -
Vegetation Patterns of Eastern South Australia : Edaphic Control and Effects of Herbivory
ì ,>3.tr .qF VEGETATION PATTERNS OF EASTERN SOUTH AUSTRALIA: EDAPHIC CONTROL &. EFFECTS OF HERBIVORY by Fleur Tiver Department of Botany The University of Adelaide A thesis submitted to the University of Adelaide for the degree of Doctor of Philosophy ar. The University of Adelaide (Faculty of Science) March 1994 dlq f 5 þø,.^roÅe*l *' -f; ri:.f.1 Frontispiece The Otary Ranges in eastern und is near the Grampus Range, and the the torvn of Yunta. The Pho TABLE OF CONTENTS Page: Title & Frontispiece i Table of Contents 11 List of Figures vll List of Tables ix Abstract x Declaration xüi Acknowledgements xiv Abbreviations & Acronyms xvü CHAPTER 1: INTRODUCTION & SCOPE OF THE STUDY INTRODUCTION 1 VEGETATION AS NATURAL HERITAGE 1 ARID VEGETATION ) RANGELANDS 3 TTTE STUDY AREA 4 A FRAMEWORK FOR THIS STUDY 4 CONCLUSION 5 CHAPTER 2: THE THEORY OF VEGETATION SCIENCE INTRODUCTION 6 INDUCTTVE, HOLIS TIC, OB S ERVATIONAL & S YNECOLOGICAL VERSUS DEDU CTIVE, EXPERIMENTAL, REDUCTIONI S T & AUTECOLOGICAL RESEARCH METHODS 7 TT{E ORGANISMIC (ECOSYSTEM) AND INDIVIDUALISTIC (CONTINUUM) CONCEPTS OF VEGETATION 9 EQUILIBRruM & NON-EQUILIBRruM CONTROL OF VEGETATON PATTERNS T3 EQUILIBRruM VS STATE-AND-TRANSITON MODELS OF VEGETATON DYNAMICS 15 CONCLUSIONS 16 11 CHAPTER 3: METHODS IN VEGETATION SCIENCE INTRODUCTION t7 ASPECT & SCALE OF VEGETATION STUDIES t7 AUTECOT-OGY Crr-rE STUDY OF POPULATTONS) & SYNEC:OLOGY (TI{E STUDY OF CTfMML'NTTTES) - A QUESTION OF SCALE l8 AGE-CLASS & STAGE-CLASS DISTRIBUTIONS IN POPULATION STUDIES t9 NUMERICAL (OBJECTIVE) VS DES CRIPTIVE (SUBJECTTVE) TECHNIQUES 20 PHYSIOGNOMIC & FLORISTIC METHODS OF VEGETATION CLASSIFICATON 22 SCALE OF CLASSIFICATION 24 TYPES OF ORDINATON 26 CIOMBINATION OF CLASSIFICATION & ORDINATION (COMPLEMENTARY ANALY SIS ) 27 CONCLUSIONS 28 CHAPTER 4: STUDY AREA . -
A Molecular Phylogeny of the Solanaceae
TAXON 57 (4) • November 2008: 1159–1181 Olmstead & al. • Molecular phylogeny of Solanaceae MOLECULAR PHYLOGENETICS A molecular phylogeny of the Solanaceae Richard G. Olmstead1*, Lynn Bohs2, Hala Abdel Migid1,3, Eugenio Santiago-Valentin1,4, Vicente F. Garcia1,5 & Sarah M. Collier1,6 1 Department of Biology, University of Washington, Seattle, Washington 98195, U.S.A. *olmstead@ u.washington.edu (author for correspondence) 2 Department of Biology, University of Utah, Salt Lake City, Utah 84112, U.S.A. 3 Present address: Botany Department, Faculty of Science, Mansoura University, Mansoura, Egypt 4 Present address: Jardin Botanico de Puerto Rico, Universidad de Puerto Rico, Apartado Postal 364984, San Juan 00936, Puerto Rico 5 Present address: Department of Integrative Biology, 3060 Valley Life Sciences Building, University of California, Berkeley, California 94720, U.S.A. 6 Present address: Department of Plant Breeding and Genetics, Cornell University, Ithaca, New York 14853, U.S.A. A phylogeny of Solanaceae is presented based on the chloroplast DNA regions ndhF and trnLF. With 89 genera and 190 species included, this represents a nearly comprehensive genus-level sampling and provides a framework phylogeny for the entire family that helps integrate many previously-published phylogenetic studies within So- lanaceae. The four genera comprising the family Goetzeaceae and the monotypic families Duckeodendraceae, Nolanaceae, and Sclerophylaceae, often recognized in traditional classifications, are shown to be included in Solanaceae. The current results corroborate previous studies that identify a monophyletic subfamily Solanoideae and the more inclusive “x = 12” clade, which includes Nicotiana and the Australian tribe Anthocercideae. These results also provide greater resolution among lineages within Solanoideae, confirming Jaltomata as sister to Solanum and identifying a clade comprised primarily of tribes Capsiceae (Capsicum and Lycianthes) and Physaleae. -
Gene Duplications and Genomic Conflict Underlie Major Pulses of Phenotypic 2 Evolution in Gymnosperms 3 4 Gregory W
bioRxiv preprint doi: https://doi.org/10.1101/2021.03.13.435279; this version posted March 15, 2021. 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-NC-ND 4.0 International license. 1 1 Gene duplications and genomic conflict underlie major pulses of phenotypic 2 evolution in gymnosperms 3 4 Gregory W. Stull1,2,†, Xiao-Jian Qu3,†, Caroline Parins-Fukuchi4, Ying-Ying Yang1, Jun-Bo 5 Yang2, Zhi-Yun Yang2, Yi Hu5, Hong Ma5, Pamela S. Soltis6, Douglas E. Soltis6,7, De-Zhu Li1,2,*, 6 Stephen A. Smith8,*, Ting-Shuang Yi1,2,*. 7 8 1Germplasm Bank of Wild Species, Kunming Institute of Botany, Chinese Academy of Sciences, 9 Kunming, Yunnan, China. 10 2CAS Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of 11 Botany, Chinese Academy of Sciences, Kunming, China. 12 3Shandong Provincial Key Laboratory of Plant Stress Research, College of Life Sciences, 13 Shandong Normal University, Jinan, Shandong, China. 14 4Department of Geophysical Sciences, University of Chicago, Chicago, IL, USA. 15 5Department of Biology, Huck Institutes of the Life Sciences, Pennsylvania State University, 16 University Park, PA, USA. 17 6Florida Museum of Natural History, University of Florida, Gainesville, FL, USA. 18 7Department of Biology, University of Florida, Gainesville, FL, USA. 19 8Department of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, 20 MI, USA. 21 †Co-first author. 22 *Correspondence to: [email protected]; [email protected]; [email protected]. -
Native Species
Birdlife Australia Gluepot Reserve PLANT SPECIES LIST These are species recorded by various observers. Species in bold have been vouchered. The list is being continually updated NATIVE SPECIES Species name Common name Acacia acanthoclada Harrow Wattle Acacia aneura Mulga Acacia brachybotrya Grey Mulga Acacia colletioides Wait a While Acacia hakeoides Hakea leaved Wattle Acacia halliana Hall’s Wattle Acacia ligulata Sandhill Wattle Acacia nyssophylla Prickly Wattle Acacia oswaldii Boomerang Bush Acacia rigens Needle Wattle Acacia sclerophylla var. sclerophylla Hard Leaved Wattle Acacia wilhelmiana Wilhelm’s Wattle Actinobole uliginosum Flannel Cudweed Alectryon oleifolius ssp. canescens Bullock Bush Amphipogon caricinus Long Grey Beard Grass Amyema miquelii Box Mistletoe Amyema miraculosa ssp. boormanii Fleshy Mistletoe Amyema preissii Wire Leaved Acacia Mistletoe Angianthus tomentosus Hairy Cup Flower Atriplex acutibractea Pointed Salt Bush Atriplex rhagodioides Spade Leaved Salt Bush Atriplex stipitata Bitter Salt Bush Atriplex vesicaria Bladder Salt Bush Austrodanthonia caespitosa Wallaby Grass Austrodanthonia pilosa Wallaby Grass Austrostipa elegantissima Elegant Spear Grass Austrostipa hemipogon Half Beard Spear grass Austrostipa nitida Balcarra Spear grass Austrostipa scabra ssp. falcata Rough Spear Grass Austrostipa scabra ssp. scabra Rough Spear Grass Austrostipa tuckeri Tucker’s Spear grass Baeckea crassifolia Desert Baeckea Baeckea ericaea Mat baeckea Bertya tasmanica ssp vestita Mitchell’s Bertya Beyeria lechenaultii Mallefowl -
Nanya Station, Western New South Wales Vegetation, Flora and Fauna
NANYA STATION, WESTERN NEW SOUTH WALES VEGETATION, FLORA AND FAUNA Prepared by Martin E. Westbrooke, Centre for Environmental Management, University of Ballarat Nanya Station, owned and managed by the University of Ballarat was purchased with assistance from the Department of Environment and Heritage. Ongoing management is supported by the Lower Murray Darling Catchment Management Authority FOREWORD 1 FOREWORD This booklet has been prepared as an introduction for visitors to Nanya. Nanya is managed for conservation, research and teaching and affords protection to highly significant environments including two endangered communities and seventeen endangered or vulnerable species. On your visit, please respect these values. NANYA STATION Nanya Station is located in the Scotia country of far western New South Wales and consists of the Nanya Western Lands Pastoral Lease 3281 – Perpetual Leasehold Lot 1244 in Deposited Plan 762778, Parish of Winnebaga, County of Tara. Nanya Homestead complex 2 BACKGROUND The Scotia region has one of the shortest stock grazing histories of western NSW. Along with five other properties, Nanya was created as a pastoral lease in 1927. Previously the area was part of the large Lake Victoria lease and stock grazing occurred only in wet years (Withers 1989). The original lease was taken up by Gordon Cummings in 1927. He first dug a dam near the southeast corner of the property. A larger ground tank and homestead at the site of the present complex was later established. An area around the homestead was cleared and cropped to provide feed for the horses used in digging the earth tanks. The ruins of the original building are located between the shearing shed and Homestead Tank. -
Eyre Peninsula NRM Board PEST SPECIES REGIONAL MANAGEMENT PLAN Lycium Ferocissimum African Boxthorn
Eyre Peninsula NRM Board PEST SPECIES REGIONAL MANAGEMENT PLAN Lycium ferocissimum African Boxthorn INTRODUCTION Synonym(s) Origin Lycium macrocalyx Domin., Lycium europaeum L. Lycium ferocissimum is native to the western and eastern (misapplied by Bailey, F.M. 1901, The Queensland Flora. 4: Cape Provinces of South Africa and the adjoining country of 1094.), Lycium chinense auct. non Mill.:Benth., partly. Lesotho [3]. Worldwide the introduced range includes Boksdorn, boxthorn. Morocco and Tunisia, south west Spain and Cyprus, Massachusetts, North Carolina and Florida in the USA, and Biology New Zealand [4]. In 1858 African boxthorn was established at the Adelaide African boxthorn Lycium ferocissimum Miers (Family Botanic Gardens, and was planted extensively as a Solanaceae) is an erect, intricately branched, semi- windbreak [5]. deciduous, perennial shrub up to five metres high, with rigid branches [1, 2]. Spines up to 15 cm long occur on the main stems, with smaller spines on the branchlets, which Distribution terminate in a spine [2]. African boxthorn has an extensive, In Australia, Lycium ferocissimum is a widespread introduced deep, root system [2]. Established plants produce suckers or weed in all but the driest and tropical regions, being found shoots from roots, including root fragments. African in all states and mainland territories [6] (Figure 1). It can boxthorn reproduces from seed. One or two flowers grow occur where the average annual rainfall is greater than 200 from leaf axils [2]. Flowering and fruiting occur mainly in mm and can be particularly abundant in wetter areas [7]. spring and summer (Table 1) [2], but are sporadic throughout the year [1]. -
Aridity Drove the Evolution of Extreme Embolism Resistance and The
Aridity drove the evolution of extreme embolism resistance and the radiation of conifer genus Callitris Maximilian Larter, Sebastian Pfautsch, Jean-Christophe Domec, Santiago Trueba, Nathalie Nagalingum, Sylvain Delzon To cite this version: Maximilian Larter, Sebastian Pfautsch, Jean-Christophe Domec, Santiago Trueba, Nathalie Na- galingum, et al.. Aridity drove the evolution of extreme embolism resistance and the radiation of conifer genus Callitris. New Phytologist, Wiley, 2017, 215 (1), pp.97-112. 10.1111/nph.14545. hal-01606790 HAL Id: hal-01606790 https://hal.archives-ouvertes.fr/hal-01606790 Submitted on 19 Nov 2019 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Distributed under a Creative Commons Attribution - ShareAlike| 4.0 International License Research Aridity drove the evolution of extreme embolism resistance and the radiation of conifer genus Callitris Maximilian Larter1, Sebastian Pfautsch2, Jean-Christophe Domec3,4, Santiago Trueba5,6, Nathalie Nagalingum7 and Sylvain Delzon1 1BIOGECO, INRA, Univ. Bordeaux, Pessac 33610, France; 2Hawkesbury Institute for the Environment, Western Sydney University, Locked Bag 1797, Penrith, NSW 2751, Australia; 3Bordeaux Sciences AGRO, UMR 1391 ISPA INRA, 1 Cours du General de Gaulle, Gradignan Cedex 33175, France; 4Nicholas School of the Environment, Duke University, Durham, NC 27708, USA; 5Department of Ecology and Evolutionary Biology, University of California, Los Angeles, UCLA, 621 Charles E. -
Images from the Outback
Images from the Outback Item Type Article Authors Johnson, Matthew B. Publisher University of Arizona (Tucson, AZ) Journal Desert Plants Rights Copyright © Arizona Board of Regents. The University of Arizona. Download date 26/09/2021 00:25:31 Link to Item http://hdl.handle.net/10150/555917 Outback Johnson 21 species of Acacia are found in Australia (Orchard and Images from the Outback - Wilson, 200 I ), though only a relatively small percentage of Notes on Plants of the Australian these occur in desert habitats. Acacia woodlands can be dense or open, and are sometimes mixed with grasses including Dry Zone spinifex. Spinifex grasslands, dominated by species of Plectraclme and Triodia (p. 27) are widespread on sandy plains as well as rocky slopes and sand dunes. These grasses, Matthew B. Johnson many with stiff, rolled leaves that end in a sharp point, form Desert Legume Program clumps or tussocks. Fires are frequent in some spinifex The University of Arizona communities and the woody plants that grow there are 2120 East Allen Road necessarily fire-adapted. Chenopod shrublands are low stature communities composed of numerous shrubs and Tucson, AZ 85719 herbaceous plants in the Chenopodiaceae. Less widespread [email protected] than acacia woodland and spinifex grassland, this type of Yegetation is found mostly in the southern parts ofAustralia's A visit to the Sydney area of Australia in 1987 tirst sparked arid zone (Van Oosterzee, 1991 ). Beyond the deserts lie my interest in seeing more of the Island Continent and in semi-arid woodlands dominated by species of Euca~vptus particular, the extensive dry regions of the country. -
The Evolution of Cavitation Resistance in Conifers Maximilian Larter
The evolution of cavitation resistance in conifers Maximilian Larter To cite this version: Maximilian Larter. The evolution of cavitation resistance in conifers. Bioclimatology. Univer- sit´ede Bordeaux, 2016. English. <NNT : 2016BORD0103>. <tel-01375936> HAL Id: tel-01375936 https://tel.archives-ouvertes.fr/tel-01375936 Submitted on 3 Oct 2016 HAL is a multi-disciplinary open access L'archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destin´eeau d´ep^otet `ala diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publi´esou non, lished or not. The documents may come from ´emanant des ´etablissements d'enseignement et de teaching and research institutions in France or recherche fran¸caisou ´etrangers,des laboratoires abroad, or from public or private research centers. publics ou priv´es. THESE Pour obtenir le grade de DOCTEUR DE L’UNIVERSITE DE BORDEAUX Spécialité : Ecologie évolutive, fonctionnelle et des communautés Ecole doctorale: Sciences et Environnements Evolution de la résistance à la cavitation chez les conifères The evolution of cavitation resistance in conifers Maximilian LARTER Directeur : Sylvain DELZON (DR INRA) Co-Directeur : Jean-Christophe DOMEC (Professeur, BSA) Soutenue le 22/07/2016 Devant le jury composé de : Rapporteurs : Mme Amy ZANNE, Prof., George Washington University Mr Jordi MARTINEZ VILALTA, Prof., Universitat Autonoma de Barcelona Examinateurs : Mme Lisa WINGATE, CR INRA, UMR ISPA, Bordeaux Mr Jérôme CHAVE, DR CNRS, UMR EDB, Toulouse i ii Abstract Title: The evolution of cavitation resistance in conifers Abstract Forests worldwide are at increased risk of widespread mortality due to intense drought under current and future climate change. -
Rangelands, Western Australia
Biodiversity Summary for NRM Regions Species List What is the summary for and where does it come from? This list has been produced by the Department of Sustainability, Environment, Water, Population and Communities (SEWPC) for the Natural Resource Management Spatial Information System. The list was produced using the AustralianAustralian Natural Natural Heritage Heritage Assessment Assessment Tool Tool (ANHAT), which analyses data from a range of plant and animal surveys and collections from across Australia to automatically generate a report for each NRM region. Data sources (Appendix 2) include national and state herbaria, museums, state governments, CSIRO, Birds Australia and a range of surveys conducted by or for DEWHA. For each family of plant and animal covered by ANHAT (Appendix 1), this document gives the number of species in the country and how many of them are found in the region. It also identifies species listed as Vulnerable, Critically Endangered, Endangered or Conservation Dependent under the EPBC Act. A biodiversity summary for this region is also available. For more information please see: www.environment.gov.au/heritage/anhat/index.html Limitations • ANHAT currently contains information on the distribution of over 30,000 Australian taxa. This includes all mammals, birds, reptiles, frogs and fish, 137 families of vascular plants (over 15,000 species) and a range of invertebrate groups. Groups notnot yet yet covered covered in inANHAT ANHAT are notnot included included in in the the list. list. • The data used come from authoritative sources, but they are not perfect. All species names have been confirmed as valid species names, but it is not possible to confirm all species locations.