BFS346 Site Species List

Total Page:16

File Type:pdf, Size:1020Kb

BFS346 Site Species List Species lists based on plot records from DEP (1996), Gibson et al. (1994), Griffin (1993), Keighery (1996) and Weston et al. (1992). Taxonomy and species attributes according to Keighery et al. (2006) as of 16th May 2005. Species Name Common Name Family Wd? Major Plant Group Significant Species Endemic Growth Form Code Growth Form Life Form Life Form - aquatics Common SSCP Wetland Species No BFS MTB0y (FCT24) MTB02 (FCT24) MTB03 (FCT24) MTB04 (FCT24) MTB05 (FCT17) NAVB0y (FCT16) NAVB02 (FCT29a) NAVB03 (FCT24) NAVB04 (FCT24) Acacia cochlearis Rigid Wattle Mimosaceae Dicot WA 3 SH P 346 y Acacia lasiocarpa Panjang Mimosaceae Dicot WA 3 SH P 346 y Acacia rostellifera Summer-scented Wattle Mimosaceae Dicot WA 3 SH/T P 346 y y Acacia saligna Coojong Mimosaceae Dicot WA 3 SH P 346 y Acanthocarpus preissii Prickle Lily Dasypogonaceae Monocot WA 4 H-SH P 346 y y * Aira caryophyllea Silvery Hairgrass Poaceae Monocot 5 G A 346 y y y y * Anagallis arvensis Pimpernel Primulaceae Dicot 4 H A 346yyyy yyy Apium annuum Annual Apium Apiaceae Dicot 4 H A 346 y Apium prostratum var. prostratum Sea Celery Apiaceae Dicot 4 H P 346 y * Arenaria leptoclados Thyme-leaved Sandwort Caryophyllaceae Dicot 4 H A 346yyyy y Arthropodium capillipes Summer Lily Anthericaceae Monocot WA 4 H PAB 346 y Atriplex cinerea Grey Saltbush Chenopodiaceae Dicot AUST 3 SH P 346 y Austrostipa flavescens Tall Speargrass Poaceae Monocot AUST 5 G P 346 y y y y * Avellinia michelii Avellinia Poaceae Monocot 5 G A 346 y y y * Avena barbata Bearded Oat Poaceae Monocot 5 G A 346 y * Avena fatua Wild Oat Poaceae Monocot 5 G A 346 y y Banksia attenuata Candle Banksia Proteaceae Dicot WA 1 T P 346 y * Bartsia trixago Bartsia Scrophulariaceae Dicot 4 H A 346 y Baumea juncea Bare Twigrush Cyperaceae Monocot AUST 6 S-C P y 346 y y * Brassica tournefortii Prickly Turnip Brassicaceae Dicot 4 H A 346 y * Briza maxima Blowfly Grass Poaceae Monocot 5 G A 346 y y y y y * Briza minor Shivery Grass Poaceae Monocot 5 G A 346 y y * Bromus diandrus Great Brome Poaceae Monocot 5 G A 346 y y y y y * Bromus hordeaceus Soft Brome Poaceae Monocot 5 G A 346 y Burchardia congesta Kara Colchicaceae Monocot WA 4 H PAB 346 y Caladenia flava subsp. flava Cowslip Orchid Orchidaceae Monocot WA 4 H PAB 346 y Caladenia latifolia Pink Fairy Orchid Orchidaceae Monocot WA 4 H PAB 346 y y Calandrinia calyptrata Pink Purslane Portulacaceae Dicot AUST 4 H A 346 y Calandrinia corrigioloides Strap Purslane Portulacaceae Dicot AUST 4 H A 346 y * Carpobrotus edulis Hottentot Fig Aizoaceae Dicot 3 SH-H (PR) P 346 y Cassytha flava Dodder Laurel Lauraceae Dicot WA 4 H (CL) P-PAR 346 y y Cassytha racemosa Dodder Laurel Lauraceae Dicot AUST 4 H (CL) P-PAR 346 y y y * Centaurea melitensis Maltese Cockspur Asteraceae Dicot 4 H A 346 y * Centaurium erythraea Centaury Gentianaceae Dicot 4 H A 346 y y y Centrolepis drummondiana Sand Centrolepis Centrolepidaceae Monocot AUST 6 S-C A 346 y * Cerastium glomeratum Sticky Mouse-ear Chickweed Caryophyllaceae Dicot 4 H A 346yyyy yyy Chamaescilla corymbosa var. corymbosa Blue Squill Anthericaceae Monocot 4 H PAB 346 y Clematis pubescens Old Man's Beard Ranunculaceae Dicot WA 4 H-SH (CL) P 346 y Page 1 of 4 Species lists based on plot records from DEP (1996), Gibson et al. (1994), Griffin (1993), Keighery (1996) and Weston et al. (1992). Taxonomy and species attributes according to Keighery et al. (2006) as of 16th May 2005. Species Name Common Name Family Wd? Major Plant Group Significant Species Endemic Growth Form Code Growth Form Life Form Life Form - aquatics Common SSCP Wetland Species No BFS MTB0y (FCT24) MTB02 (FCT24) MTB03 (FCT24) MTB04 (FCT24) MTB05 (FCT17) NAVB0y (FCT16) NAVB02 (FCT29a) NAVB03 (FCT24) NAVB04 (FCT24) Comesperma confertum Coastal Comesperma Polygalaceae Dicot WA 3 SH-H P 346 y y Conostylis aculeata Prickly Conostylis Haemodoraceae Monocot WA 4 H P 346 y y Conostylis candicans subsp. candicans Grey Conostylis Haemodoraceae Monocot WA 4 H P 346 y * Conyza bonariensis Fleabane Asteraceae Dicot 4 H A 346 y y * Conyza sumatrensis Fleabane Asteraceae Dicot 4 H A 346 y y Crassula colorata var. colorata Dense Stonecrop Crassulaceae Dicot AUST 4 H A 346 y y y y y * Crassula glomerata Stonecrop Crassulaceae Dicot 4 H A 346 y y y y y Cryptandra mutila Cryptandra Rhamnaceae Dicot WA 3 SH P 346 y Daucus glochidiatus Australian Carrot Apiaceae Dicot 4 H A 346 y Daviesia triflora Three-flowered Daviesia Papilionaceae Dicot WA 3 SH P 346 y * Desmazeria rigida Rigid Fescue Poaceae Monocot 5 G A 346 y y Desmocladus flexuosus Desmocladus Restionaceae Monocot 6 S-R P 346 y y y * Disa bracteata South African Orchid Orchidaceae Monocot 4 H PAB 346 y * Dischisma arenarium Dischisma Scrophulariaceae Dicot 4 H A 346 y y Drosera erythrorhiza subsp. erythrorhiza Red Ink Sundew Droseraceae Dicot WA 4 H PAB 346 y y Drosera pallida Rainbow Droseraceae Dicot WA 4 H PAB 346 y y y Dryandra lindleyana Couch Honeypot Proteaceae Dicot WA 3 SH (PR) P 346yy yy Dryandra sessilis var. sessilis Hills Parrotbush Proteaceae Dicot WA 3 SH P 346 y * Ehrharta calycina Perennial Veldtgrass Poaceae Monocot 5 G P 346 y * Ehrharta longiflora Annual Veldtgrass Poaceae Monocot 5 G A 346 y y y Eremophila glabra subsp. albicans Eremophila Myoporaceae Dicot WA 3 SH P 346 y * Erodium cicutarium Common Storksbill Geraniaceae Dicot 4 H A 346 y Eucalyptus decipiens subsp. decipiens Limestone Marlock Myrtaceae Dicot WA 2 M P 346 y Eucalyptus gomphocephala var. gomphocephala Tuart Myrtaceae Dicot WA 1 T/M P 346 y Eucalyptus marginata subsp. marginata Jarrah Myrtaceae Dicot WA 1 T P 346 y * Euphorbia peplus Petty Spurge Euphorbiaceae Dicot 4 H A 346 y y y Ficinia nodosa Knotted Clubrush Cyperaceae Monocot AUST 6 S-C P 346 y Frankenia pauciflora Sea Heath Frankeniaceae Dicot AUST 3 SH P 346 y y Gahnia trifida Coast Sawsedge Cyperaceae Monocot AUST 6 S-C P y 346 y * Galium aparine Goosegrass Rubiaceae Dicot 4 H A 346 y y * Galium murale Bedstraw Rubiaceae Dicot 4 H A 346yyyy y Gastrolobium capitatum Common Nemcia Papilionaceae Dicot WA 3 SH P 346 y Gompholobium tomentosum Common Gompholobium Papilionaceae Dicot WA 3 SH P 346 y y Grevillea preissii subsp. preissii Limestone Spider-net Grevillea Proteaceae Dicot WA 3 SH P 346yy yyy Hakea prostrata Harsh Hakea Proteaceae Dicot WA 3 SH P 346 y Hardenbergia comptoniana Hardenbergia Papilionaceae Dicot WA 3 SH (CL) P 346yyyy yy * Heliophila pusilla Heliophila Brassicaceae Dicot 4 H A 346 y Hibbertia hypericoides Common Hibbertia Dilleniaceae Dicot WA 3 SH P 346 y y y Page 2 of 4 Species lists based on plot records from DEP (1996), Gibson et al. (1994), Griffin (1993), Keighery (1996) and Weston et al. (1992). Taxonomy and species attributes according to Keighery et al. (2006) as of 16th May 2005. Species Name Common Name Family Wd? Major Plant Group Significant Species Endemic Growth Form Code Growth Form Life Form Life Form - aquatics Common SSCP Wetland Species No BFS MTB0y (FCT24) MTB02 (FCT24) MTB03 (FCT24) MTB04 (FCT24) MTB05 (FCT17) NAVB0y (FCT16) NAVB02 (FCT29a) NAVB03 (FCT24) NAVB04 (FCT24) Hibbertia racemosa Stalked Hibbertia Dilleniaceae Dicot WA 3 SH P 346 y y Hibbertia spicata subsp. leptotheca Limestone Hibbertia Dilleniaceae Dicot P3/p,s,e WA 3 SH P 346 y Homalosciadium homalocarpum Homahoma Apiaceae Dicot WA 4 H A 346 y Hyalosperma cotula Hyalosperma Asteraceae Dicot WA 4 H A 346 y Hybanthus calycinus Native Violet Violaceae Dicot WA 4 H-SH P 346 y y Hydrocotyle diantha Pennywort Apiaceae Dicot WA 4 H A 346 y * Hypochaeris glabra Flatweed Asteraceae Dicot 4 H A 346yyyy yy Isolepis cernua Nodding Clubrush Cyperaceae Monocot AUST 6 S-C A 346 y y y y y y Kennedia coccinea Coral Kennedia Papilionaceae Dicot s WA 4 H (PR) P 346 y * Lagurus ovatus Hare's Tail Grass Poaceae Monocot 5 G A 346yy yy 231) Lepidosperma Cyperaceae Monocot WA 6 S-C P 346 y Lepidosperma squamatum Common Lepidosperma Cyperaceae Monocot WA 6 S-C P 346 y y y y Leucopogon parviflorus Beard Heath Epacridaceae Dicot WA 3 SH P 346 y y y * Lolium rigidum Annual Ryegrass Poaceae Monocot 5 G A 346 y y Lomandra maritima Coast Lomandra Dasypogonaceae Monocot WA 4 H P 346 y y y y Lyginia barbata Lyginia Restionaceae Monocot 6 S-R P 346 y y Macrozamia riedlei Riedlé's Zamia Zamiaceae Cycad WA 3 SH-H P 346 y y Meeboldina coangustata Meeboldina Restionaceae Monocot 6 S-R P y 346 y Melaleuca huegelii subsp. huegelii Chenille Honeymyrtle Myrtaceae Dicot WA 3 SH P 346 y y Melaleuca rhaphiophylla Freshwater Paperbark Myrtaceae Dicot WA 3 SH P y 346 y Melaleuca systena Yellow Honeymyrtle Myrtaceae Dicot WA 3 SH P 346yy yy Melaleuca teretifolia Swamp Honeymyrtle Myrtaceae Dicot WA 3 SH P y 346 y * Melilotus indicus Common Melilot Papilionaceae Dicot 4 H A 346 y y Mesomelaena pseudostygia Semaphore Sedge Cyperaceae Monocot WA 6 S-C P 346 y Microlaena stipoides Weeping Grass Poaceae Monocot AUST 5 G P 346 y Millotia tenuifolia var. tenuifolia Soft Millotia Asteraceae Dicot AUST 4 H A 346 y y * Minuartia mediterranea Sandwort Caryophyllaceae Dicot 4 H A 346 y y * Moraea flaccida One-leaf Cape Tulip Iridaceae Monocot 4 H PAB 346 y y Nemcia reticulata Reticulate Nemcia Papilionaceae Dicot WA 3 SH P 346 y Olearia axillaris Coastal Daisybush Asteraceae Dicot AUST 3 SH P 346 y Opercularia vaginata Opercularia Rubiaceae Dicot WA 3 SH-H P 346 y * Orobanche minor Broom Rape Orobanchaceae Dicot 4 H A-PAR 346 y * Parentucellia viscosa Sticky Bartsia Scrophulariaceae Dicot 4 H A 346 y * Pelargonium capitatum Rose Pelargonium Geraniaceae Dicot 4 H-SH P 346 y Pelargonium littorale subsp.
Recommended publications
  • The Vascular Plants of Massachusetts
    The Vascular Plants of Massachusetts: The Vascular Plants of Massachusetts: A County Checklist • First Revision Melissa Dow Cullina, Bryan Connolly, Bruce Sorrie and Paul Somers Somers Bruce Sorrie and Paul Connolly, Bryan Cullina, Melissa Dow Revision • First A County Checklist Plants of Massachusetts: Vascular The A County Checklist First Revision Melissa Dow Cullina, Bryan Connolly, Bruce Sorrie and Paul Somers Massachusetts Natural Heritage & Endangered Species Program Massachusetts Division of Fisheries and Wildlife Natural Heritage & Endangered Species Program The Natural Heritage & Endangered Species Program (NHESP), part of the Massachusetts Division of Fisheries and Wildlife, is one of the programs forming the Natural Heritage network. NHESP is responsible for the conservation and protection of hundreds of species that are not hunted, fished, trapped, or commercially harvested in the state. The Program's highest priority is protecting the 176 species of vertebrate and invertebrate animals and 259 species of native plants that are officially listed as Endangered, Threatened or of Special Concern in Massachusetts. Endangered species conservation in Massachusetts depends on you! A major source of funding for the protection of rare and endangered species comes from voluntary donations on state income tax forms. Contributions go to the Natural Heritage & Endangered Species Fund, which provides a portion of the operating budget for the Natural Heritage & Endangered Species Program. NHESP protects rare species through biological inventory,
    [Show full text]
  • Partial Flora Survey Rottnest Island Golf Course
    PARTIAL FLORA SURVEY ROTTNEST ISLAND GOLF COURSE Prepared by Marion Timms Commencing 1 st Fairway travelling to 2 nd – 11 th left hand side Family Botanical Name Common Name Mimosaceae Acacia rostellifera Summer scented wattle Dasypogonaceae Acanthocarpus preissii Prickle lily Apocynaceae Alyxia Buxifolia Dysentry bush Casuarinacea Casuarina obesa Swamp sheoak Cupressaceae Callitris preissii Rottnest Is. Pine Chenopodiaceae Halosarcia indica supsp. Bidens Chenopodiaceae Sarcocornia blackiana Samphire Chenopodiaceae Threlkeldia diffusa Coast bonefruit Chenopodiaceae Sarcocornia quinqueflora Beaded samphire Chenopodiaceae Suada australis Seablite Chenopodiaceae Atriplex isatidea Coast saltbush Poaceae Sporabolis virginicus Marine couch Myrtaceae Melaleuca lanceolata Rottnest Is. Teatree Pittosporaceae Pittosporum phylliraeoides Weeping pittosporum Poaceae Stipa flavescens Tussock grass 2nd – 11 th Fairway Family Botanical Name Common Name Chenopodiaceae Sarcocornia quinqueflora Beaded samphire Chenopodiaceae Atriplex isatidea Coast saltbush Cyperaceae Gahnia trifida Coast sword sedge Pittosporaceae Pittosporum phyliraeoides Weeping pittosporum Myrtaceae Melaleuca lanceolata Rottnest Is. Teatree Chenopodiaceae Sarcocornia blackiana Samphire Central drainage wetland commencing at Vietnam sign Family Botanical Name Common Name Chenopodiaceae Halosarcia halecnomoides Chenopodiaceae Sarcocornia quinqueflora Beaded samphire Chenopodiaceae Sarcocornia blackiana Samphire Poaceae Sporobolis virginicus Cyperaceae Gahnia Trifida Coast sword sedge
    [Show full text]
  • Restoration After Removal of Pines at Gnangara Final
    RESTORATION OF BANKSIA WOODLAND AFTER THE REMOVAL OF PINES AT GNANGARA: SEED SPECIES REQUIREMENTS AND PRESCRIPTIONS FOR RESTORATION A report prepared on behalf of the Department of Environment and Conservation for the Gnangara Sustainability Strategy Kellie Maher University of Western Australia May 2009 Restoration of Banksia woodland after the removal of pines at Gnangara: seed species requirements and prescriptions for restoration Report for the Department of Environment and Conservation Kellie Maher University of Western Australia Gnangara Sustainability Strategy Taskforce Department of Water 168 St Georges Terrace Perth Western Australia 6000 Telephone +61 8 6364 7600 Facsimile +61 8 6364 7601 www.gnangara.water.wa.gov.au © Government of Western Australia 2009 May 2009 This work is copyright. You may download, display, print and reproduce this material in unaltered form only (retaining this notice) for your personal, non-commercial use or use within your organisation. Apart from any use as permitted under the Copyright Act 1968 , all other rights are reserved. Requests and inquiries concerning reproduction and rights should be addressed to the Department of Conservation and Environment. This document has been commissioned/produced as part of the Gnangara Sustainability Strategy (GSS). The GSS is a State Government initiative which aims to provide a framework for a whole of government approach to address land use and water planning issues associated with the Gnangara groundwater system. For more information go to www.gnangara.water.wa.gov.au 1 Restoration of Banksia woodland after the removal of pines at Gnangara: seed species requirements and prescriptions for restoration A report to the Department of Environment and Conservation Kellie Maher University of Western Australia May 2009 2 Table of Contents List of Tables ....................................................................................................................
    [Show full text]
  • Native Orchid Society South Australia
    Journal of the Native Orchid Society of South Australia Inc Print Post Approved .Volume 37 Nº 8 PP 543662/00018 September 2013 NATIVE ORCHID SOCIETY OF SOUTH AUSTRALIA PO BOX 565 UNLEY SA 5061 www.nossa.org.au. The Native Orchid Society of South Australia promotes the conservation of orchids through the preservation of natural habitat and through cultivation. Except with the documented official representation of the management committee, no person may represent the Society on any matter. All native orchids are protected in the wild; their collection without written Government permit is illegal. PRESIDENT SECRETARY Geoffrey Borg: John Bartram Email. [email protected] Email: [email protected] VICE PRESIDENT Kris Kopicki COMMITTEE Jan Adams Bob Bates Robert Lawrence Rosalie Lawrence EDITOR TREASURER David Hirst Gordon Ninnes 14 Beaverdale Avenue Telephone Windsor Gardens SA 5087 mob. Telephone 8261 7998 Email: [email protected] Email: [email protected] or [email protected] LIFE MEMBERS Mr R. Hargreaves† Mr. L. Nesbitt Mr H. Goldsack† Mr G. Carne Mr R. Robjohns† Mr R Bates Mr J. Simmons† Mr R Shooter Mr D. Wells† Mr W Dear Mrs C Houston Conservation Officer: Thelma Bridle / Bob Bates Field Trips Coordinator: Wendy Hudson. Ph: 8251 2762, Email: [email protected] Trading Table: Judy Penney Show Marshall: vacant Registrar of Judges: Les Nesbitt Tuber bank Coordinator: Jane Higgs ph. 8558 6247; email: [email protected] New Members Coordinator: Vacant PATRON Mr L. Nesbitt The Native Orchid Society of South Australia, while taking all due care, take no responsibility for loss or damage to any plants whether at shows, meetings or exhibits.
    [Show full text]
  • Their Botany, Essential Oils and Uses 6.86 MB
    MELALEUCAS THEIR BOTANY, ESSENTIAL OILS AND USES Joseph J. Brophy, Lyndley A. Craven and John C. Doran MELALEUCAS THEIR BOTANY, ESSENTIAL OILS AND USES Joseph J. Brophy School of Chemistry, University of New South Wales Lyndley A. Craven Australian National Herbarium, CSIRO Plant Industry John C. Doran Australian Tree Seed Centre, CSIRO Plant Industry 2013 The Australian Centre for International Agricultural Research (ACIAR) was established in June 1982 by an Act of the Australian Parliament. ACIAR operates as part of Australia's international development cooperation program, with a mission to achieve more productive and sustainable agricultural systems, for the benefit of developing countries and Australia. It commissions collaborative research between Australian and developing-country researchers in areas where Australia has special research competence. It also administers Australia's contribution to the International Agricultural Research Centres. Where trade names are used this constitutes neither endorsement of nor discrimination against any product by ACIAR. ACIAR MONOGRAPH SERIES This series contains the results of original research supported by ACIAR, or material deemed relevant to ACIAR’s research and development objectives. The series is distributed internationally, with an emphasis on developing countries. © Australian Centre for International Agricultural Research (ACIAR) 2013 This work is copyright. Apart from any use as permitted under the Copyright Act 1968, no part may be reproduced by any process without prior written permission from ACIAR, GPO Box 1571, Canberra ACT 2601, Australia, [email protected] Brophy J.J., Craven L.A. and Doran J.C. 2013. Melaleucas: their botany, essential oils and uses. ACIAR Monograph No. 156. Australian Centre for International Agricultural Research: Canberra.
    [Show full text]
  • BFS048 Site Species List
    Species lists based on plot records from DEP (1996), Gibson et al. (1994), Griffin (1993), Keighery (1996) and Weston et al. (1992). Taxonomy and species attributes according to Keighery et al. (2006) as of 16th May 2005. Species Name Common Name Family Major Plant Group Significant Species Endemic Growth Form Code Growth Form Life Form Life Form - aquatics Common SSCP Wetland Species BFS No kens01 (FCT23a) Wd? Acacia sessilis Wattle Mimosaceae Dicot WA 3 SH P 48 y Acacia stenoptera Narrow-winged Wattle Mimosaceae Dicot WA 3 SH P 48 y * Aira caryophyllea Silvery Hairgrass Poaceae Monocot 5 G A 48 y Alexgeorgea nitens Alexgeorgea Restionaceae Monocot WA 6 S-R P 48 y Allocasuarina humilis Dwarf Sheoak Casuarinaceae Dicot WA 3 SH P 48 y Amphipogon turbinatus Amphipogon Poaceae Monocot WA 5 G P 48 y * Anagallis arvensis Pimpernel Primulaceae Dicot 4 H A 48 y Austrostipa compressa Golden Speargrass Poaceae Monocot WA 5 G P 48 y Banksia menziesii Firewood Banksia Proteaceae Dicot WA 1 T P 48 y Bossiaea eriocarpa Common Bossiaea Papilionaceae Dicot WA 3 SH P 48 y * Briza maxima Blowfly Grass Poaceae Monocot 5 G A 48 y Burchardia congesta Kara Colchicaceae Monocot WA 4 H PAB 48 y Calectasia narragara Blue Tinsel Lily Dasypogonaceae Monocot WA 4 H-SH P 48 y Calytrix angulata Yellow Starflower Myrtaceae Dicot WA 3 SH P 48 y Centrolepis drummondiana Sand Centrolepis Centrolepidaceae Monocot AUST 6 S-C A 48 y Conostephium pendulum Pearlflower Epacridaceae Dicot WA 3 SH P 48 y Conostylis aculeata Prickly Conostylis Haemodoraceae Monocot WA 4 H P 48 y Conostylis juncea Conostylis Haemodoraceae Monocot WA 4 H P 48 y Conostylis setigera subsp.
    [Show full text]
  • Widespread Paleopolyploidy, Gene Tree Conflict, and Recalcitrant Relationships Among the 3 Carnivorous Caryophyllales1 4 5 Joseph F
    bioRxiv preprint doi: https://doi.org/10.1101/115741; this version posted March 10, 2017. 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 4.0 International license. 1 2 Widespread paleopolyploidy, gene tree conflict, and recalcitrant relationships among the 3 carnivorous Caryophyllales1 4 5 Joseph F. Walker*,2, Ya Yang2,5, Michael J. Moore3, Jessica Mikenas3, Alfonso Timoneda4, Samuel F. 6 Brockington4 and Stephen A. Smith*,2 7 8 2Department of Ecology & Evolutionary Biology, University of Michigan, 830 North University Avenue, 9 Ann Arbor, MI 48109-1048, USA 10 3Department of Biology, Oberlin College, Science Center K111, 119 Woodland St., Oberlin, Ohio 44074- 11 1097 USA 12 4Department of Plant Sciences, University of Cambridge, Cambridge CB2 3EA, United Kingdom 13 5 Department of Plant Biology, University of Minnesota-Twin Cities. 1445 Gortner Avenue, St. Paul, MN 14 55108 15 CORRESPONDING AUTHORS: Joseph F. Walker; [email protected] and Stephen A. Smith; 16 [email protected] 17 18 1Manuscript received ____; revision accepted ______. bioRxiv preprint doi: https://doi.org/10.1101/115741; this version posted March 10, 2017. 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 4.0 International license. 19 ABSTRACT 20 • The carnivorous members of the large, hyperdiverse Caryophyllales (e.g.
    [Show full text]
  • Molecular Phylogenetic Analysis Resolves Trisetum
    Journal of Systematics JSE and Evolution doi: 10.1111/jse.12523 Research Article Molecular phylogenetic analysis resolves Trisetum (Poaceae: Pooideae: Koeleriinae) polyphyletic: Evidence for a new genus, Sibirotrisetum and resurrection of Acrospelion Patricia Barberá1,3*,RobertJ.Soreng2 , Paul M. Peterson2* , Konstantin Romaschenko2 , Alejandro Quintanar1, and Carlos Aedo1 1Department of Biodiversity and Conservation, Real Jardín Botánico, CSIC, Madrid 28014, Spain 2Department of Botany, National Museum of Natural History, Smithsonian Institution, Washington DC 20013‐7012, USA 3Department of Africa and Madagascar, Missouri Botanical Garden, St. Louis, MO 63110, USA *Authors for correspondence. Patricia Barberá. E‐mail: [email protected]; Paul M. Peterson. E‐mail: [email protected] Received 4 March 2019; Accepted 5 May 2019; Article first published online 22 June 2019 Abstract To investigate the evolutionary relationships among the species of Trisetum and other members of subtribe Koeleriinae, a phylogeny based on DNA sequences from four gene regions (ITS, rpl32‐trnL spacer, rps16‐trnK spacer, and rps16 intron) is presented. The analyses, including type species of all genera in Koeleriinae (Acrospelion, Avellinia, Cinnagrostis, Gaudinia, Koeleria, Leptophyllochloa, Limnodea, Peyritschia, Rostraria, Sphenopholis, Trisetaria, Trisetopsis, Trisetum), along with three outgroups, confirm previous indications of extensive polyphyly of Trisetum. We focus on the monophyletic Trisetum sect. Sibirica cladethatweinterprethereasadistinctgenus,Sibirotrisetum gen. nov. We include adescriptionofSibirotrisetum with the following seven new combinations: Sibirotrisetum aeneum, S. bifidum, S. henryi, S. scitulum, S. sibiricum, S. sibiricum subsp. litorale,andS. turcicum; and a single new combination in Acrospelion: A. distichophyllum. Trisetum s.s. is limited to one, two or three species, pending further study. Key words: Acrospelion, Aveneae, grasses, molecular systematics, Poeae, Sibirotrisetum, taxonomy, Trisetum.
    [Show full text]
  • ALINTA DBNGP LOOPING 10 Rehabilitation Management Plan
    DBNGP (WA) Nominees Pty Ltd DBNGP LOOPING 10 Rehabilitation Management Plan ALINTA DBNGP LOOPING 10 Rehabilitation Management Plan November 2005 Ecos Consulting (Aust) Pty Ltd CONTENTS 1 INTRODUCTION ................................................................................ 1 2 REHABILITATION REVIEW............................................................ 1 2.1 REHABILITATION OBJECTIVES ............................................................... 2 3 EXISTING VEGETATION ................................................................. 2 3.1 FLORA AND VEGETATION...................................................................... 2 3.2 VEGETATION STUDIES ........................................................................... 4 3.2.1 Study Method ............................................................................... 4 3.2.2 Study Results ................................................................................ 7 3.3 OTHER ENVIRONMENTAL VALUES ...................................................... 10 4 REHABILITATION STRATEGY..................................................... 11 5 REHABILITATION METHODS ..................................................... 11 5.1 WEED MANAGEMENT.......................................................................... 11 5.2 DIEBACK (PHYTOPHTHORA CINNAMOMI) MANAGEMENT .................... 11 5.3 PRIORITY AND RARE FLORA MANAGEMENT ........................................ 12 5.4 RESOURCE MANAGEMENT ................................................................... 13 5.5
    [Show full text]
  • Special Issue3.7 MB
    Volume Eleven Conservation Science 2016 Western Australia Review and synthesis of knowledge of insular ecology, with emphasis on the islands of Western Australia IAN ABBOTT and ALLAN WILLS i TABLE OF CONTENTS Page ABSTRACT 1 INTRODUCTION 2 METHODS 17 Data sources 17 Personal knowledge 17 Assumptions 17 Nomenclatural conventions 17 PRELIMINARY 18 Concepts and definitions 18 Island nomenclature 18 Scope 20 INSULAR FEATURES AND THE ISLAND SYNDROME 20 Physical description 20 Biological description 23 Reduced species richness 23 Occurrence of endemic species or subspecies 23 Occurrence of unique ecosystems 27 Species characteristic of WA islands 27 Hyperabundance 30 Habitat changes 31 Behavioural changes 32 Morphological changes 33 Changes in niches 35 Genetic changes 35 CONCEPTUAL FRAMEWORK 36 Degree of exposure to wave action and salt spray 36 Normal exposure 36 Extreme exposure and tidal surge 40 Substrate 41 Topographic variation 42 Maximum elevation 43 Climate 44 Number and extent of vegetation and other types of habitat present 45 Degree of isolation from the nearest source area 49 History: Time since separation (or formation) 52 Planar area 54 Presence of breeding seals, seabirds, and turtles 59 Presence of Indigenous people 60 Activities of Europeans 63 Sampling completeness and comparability 81 Ecological interactions 83 Coups de foudres 94 LINKAGES BETWEEN THE 15 FACTORS 94 ii THE TRANSITION FROM MAINLAND TO ISLAND: KNOWNS; KNOWN UNKNOWNS; AND UNKNOWN UNKNOWNS 96 SPECIES TURNOVER 99 Landbird species 100 Seabird species 108 Waterbird
    [Show full text]
  • Draft Survey Guidelines for Australia's Threatened Orchids
    SURVEY GUIDELINES FOR AUSTRALIA’S THREATENED ORCHIDS GUIDELINES FOR DETECTING ORCHIDS LISTED AS ‘THREATENED’ UNDER THE ENVIRONMENT PROTECTION AND BIODIVERSITY CONSERVATION ACT 1999 0 Authorship and acknowledgements A number of experts have shared their knowledge and experience for the purpose of preparing these guidelines, including Allanna Chant (Western Australian Department of Parks and Wildlife), Allison Woolley (Tasmanian Department of Primary Industry, Parks, Water and Environment), Andrew Brown (Western Australian Department of Environment and Conservation), Annabel Wheeler (Australian Biological Resources Study, Australian Department of the Environment), Anne Harris (Western Australian Department of Parks and Wildlife), David T. Liddle (Northern Territory Department of Land Resource Management, and Top End Native Plant Society), Doug Bickerton (South Australian Department of Environment, Water and Natural Resources), John Briggs (New South Wales Office of Environment and Heritage), Luke Johnston (Australian Capital Territory Environment and Sustainable Development Directorate), Sophie Petit (School of Natural and Built Environments, University of South Australia), Melanie Smith (Western Australian Department of Parks and Wildlife), Oisín Sweeney (South Australian Department of Environment, Water and Natural Resources), Richard Schahinger (Tasmanian Department of Primary Industry, Parks, Water and Environment). Disclaimer The views and opinions contained in this document are not necessarily those of the Australian Government. The contents of this document have been compiled using a range of source materials and while reasonable care has been taken in its compilation, the Australian Government does not accept responsibility for the accuracy or completeness of the contents of this document and shall not be liable for any loss or damage that may be occasioned directly or indirectly through the use of or reliance on the contents of the document.
    [Show full text]
  • Supporting Information Appendix Pliocene Reversal of Late Neogene
    1 Supporting Information Appendix 2 Pliocene reversal of late Neogene aridification 3 4 J.M.K. Sniderman, J. Woodhead, J. Hellstrom, G.J. Jordan, R.N. Drysdale, J.J. Tyler, N. 5 Porch 6 7 8 SUPPLEMENTARY MATERIALS AND METHODS 9 10 Pollen analysis. We attempted to extract fossil pollen from 81 speleothems collected from 11 16 caves from the Western Australian portion of the Nullarbor Plain. Nullarbor speleothems 12 and caves are essentially “fossil” features that appear to have been preserved by very slow 13 rates of landscape change in a semi-arid landscape. Sample collection targeted fallen, well 14 preserved speleothems in multiple caves. U-Pb dates of these speleothems (Table S3) 15 ranged from late Miocene (8.19 Ma) to Middle Pleistocene (0.41 Ma), with an average age 16 of 4.11 Ma. 17 Fossil pollen typically is present in speleothems in very low concentrations, so pollen 18 processing techniques were developed to minimize contamination by modern pollen (1), but 19 also to maximize recovery, to accommodate the highly variable organic matter content of the 20 speleothems, and to remove a clay- to fine silt-sized mineral fraction present in many 21 samples, which was resistant to cold HF and which can become electrostatically attracted to 22 pollen grains, inhibiting their identification. Stalagmite and flowstone samples of 30-200 g 23 mass were first cut on a diamond rock saw in order to remove any obviously porous material. 24 All subsequent physical and chemical processes were carried out within a HEPA-filtered 25 exhausting clean air cabinet in an ISO Class 7 clean room.
    [Show full text]