Hepburn Heights Conservation Area Management Plan
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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 -
Tracing History
Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology 911 Tracing History Phylogenetic, Taxonomic, and Biogeographic Research in the Colchicum Family BY ANNIKA VINNERSTEN ACTA UNIVERSITATIS UPSALIENSIS UPPSALA 2003 Dissertation presented at Uppsala University to be publicly examined in Lindahlsalen, EBC, Uppsala, Friday, December 12, 2003 at 10:00 for the degree of Doctor of Philosophy. The examination will be conducted in English. Abstract Vinnersten, A. 2003. Tracing History. Phylogenetic, Taxonomic and Biogeographic Research in the Colchicum Family. Acta Universitatis Upsaliensis. Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology 911. 33 pp. Uppsala. ISBN 91-554-5814-9 This thesis concerns the history and the intrafamilial delimitations of the plant family Colchicaceae. A phylogeny of 73 taxa representing all genera of Colchicaceae, except the monotypic Kuntheria, is presented. The molecular analysis based on three plastid regions—the rps16 intron, the atpB- rbcL intergenic spacer, and the trnL-F region—reveal the intrafamilial classification to be in need of revision. The two tribes Iphigenieae and Uvularieae are demonstrated to be paraphyletic. The well-known genus Colchicum is shown to be nested within Androcymbium, Onixotis constitutes a grade between Neodregea and Wurmbea, and Gloriosa is intermixed with species of Littonia. Two new tribes are described, Burchardieae and Tripladenieae, and the two tribes Colchiceae and Uvularieae are emended, leaving four tribes in the family. At generic level new combinations are made in Wurmbea and Gloriosa in order to render them monophyletic. The genus Androcymbium is paraphyletic in relation to Colchicum and the latter genus is therefore expanded. -
Evolution of Angiosperm Pollen. 7. Nitrogen-Fixing Clade1
Evolution of Angiosperm Pollen. 7. Nitrogen-Fixing Clade1 Authors: Jiang, Wei, He, Hua-Jie, Lu, Lu, Burgess, Kevin S., Wang, Hong, et. al. Source: Annals of the Missouri Botanical Garden, 104(2) : 171-229 Published By: Missouri Botanical Garden Press URL: https://doi.org/10.3417/2019337 BioOne Complete (complete.BioOne.org) is a full-text database of 200 subscribed and open-access titles in the biological, ecological, and environmental sciences published by nonprofit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Complete website, and all posted and associated content indicates your acceptance of BioOne’s Terms of Use, available at www.bioone.org/terms-of-use. Usage of BioOne Complete content is strictly limited to personal, educational, and non - commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research. Downloaded From: https://bioone.org/journals/Annals-of-the-Missouri-Botanical-Garden on 01 Apr 2020 Terms of Use: https://bioone.org/terms-of-use Access provided by Kunming Institute of Botany, CAS Volume 104 Annals Number 2 of the R 2019 Missouri Botanical Garden EVOLUTION OF ANGIOSPERM Wei Jiang,2,3,7 Hua-Jie He,4,7 Lu Lu,2,5 POLLEN. 7. NITROGEN-FIXING Kevin S. Burgess,6 Hong Wang,2* and 2,4 CLADE1 De-Zhu Li * ABSTRACT Nitrogen-fixing symbiosis in root nodules is known in only 10 families, which are distributed among a clade of four orders and delimited as the nitrogen-fixing clade. -
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. -
Reptiles in and Around the House Identification and Distribution Reptiles Inhabit Every Environment in Australia
Reptiles in and around the house Identification and Distribution Reptiles inhabit every environment in Australia. Common reptiles found in Western Australian backyards include: Tiger snakes Notechis scutatus occur in southwest WA, and are often seen near water, including rivers, dams, drains and wetlands. Unlike most other Australian elapids, tiger snakes climb well. They can range from grey, olive, brown to black in colour and often have yellow and black cross-bands, but not all have this pattern. Venomous Dugite. Photo: R. Lloyd/Fauna Track Dugites Pseudonaja affinis occur in southwest WA and Gwarda Pseudonaja nuchalis occur from Perth northwards. They live in a wide variety of habitats including coastal dunes, heathlands, shrublands, woodlands and forests. They are long and slender, with relatively large scales that have a semi-glossy appearance. They can range from brown, olive to grey in colour, and can have irregular black/dark grey spotting, but patterning varies. Venomous Mulga snakes Pseudechis australis occur in a wide variety of habitats, northwards from Perth and Narrogin. They are quite robust, with a broad, deep head and bulbous cheeks. They can range from pale brown, dark olive to reddish-brown in colour, and darker snakes often have two-toned scales with a lighter colour that contrasts with the darker colour to produce a reticulated effect. The belly is cream to salmon-coloured. Venomous There are two subspecies of carpet pythons found in a large variety of habitats in WA: Morelia spilota imbricata occurs in the southwest and Morelia spilota variegata occurs in the Kimberley. They are 1-4m in length, tend to be pale to dark brown with black blotches that sometimes have a Carpet python. -
Venemous Snakes
WASAH WESTERN AUSTRALIAN SOCIETY of AMATEUR HERPETOLOGISTS (Inc) K E E P I N G A D V I C E S H E E T Venomous Snakes Southern Death Adder (Acanthophis Southern Death antarcticus) – Maximum length 100 cm. Adder Category 5. Desert Death Adder (Acanthophis pyrrhus) – Acanthophis antarcticus Maximum length 75 cm. Category 5. Pilbara Death Adder (Acanthophis wellsi) – Maximum length 70 cm. Category 5. Western Tiger Snake (Notechis scutatus) - Maximum length 160 cm. Category 5. Mulga Snake (Pseudechis australis) – Maximum length 300 cm. Category 5. Spotted Mulga Snake (Pseudechis butleri) – Maximum length 180 cm. Category 5. Dugite (Pseudonaja affinis affinis) – Maximum Desert Death Adder length 180 cm. Category 5. Acanthophis pyrrhus Gwardar (Pseudonaja nuchalis) – Maximum length 100 cm. Category 5. NOTE: All species listed here are dangerously venomous and are listed as Category 5. Only the experienced herpetoculturalist should consider keeping any of them. One must be over 18 years of age to hold a category 5 license. Maintaining a large elapid carries with 1 it a considerable responsibility. Unless you are Pilbara Death Adder confident that you can comply with all your obligations and licence requirements when Acanthophis wellsi keeping dangerous animals, then look to obtaining a non-venomous species instead. NATURAL HABITS: Venomous snakes occur in a wide variety of habitats and, apart from death adders, are highly mobile. All species are active day and night. HOUSING: In all species listed except death adders, one adult (to 150 cm total length) can be kept indoors in a lockable, top-ventilated, all glass or glass-fronted wooden vivarium of Western Tiger Snake at least 90 x 45 cm floor area. -
Newsletter Number 29 September 1992 New Zealand Botanical Society Newsletter Number 29 September 1992
NEW ZEALAND BOTANICAL SOCIETY NEWSLETTER NUMBER 29 SEPTEMBER 1992 NEW ZEALAND BOTANICAL SOCIETY NEWSLETTER NUMBER 29 SEPTEMBER 1992 CONTENTS News NZ Bot Soc News Call for nominations 2 New Zealand Threatened Indigenous Vascular Plant List .2 Regional Bot Soc News Auckland 5 Canterbury 6 Nelson 6 Rotorua 7 Waikato 7 Wellington 8 Obituary Margot Forde 8 Other News Distinguished New Zealand Scientist turns 100 9 Government Science structures reorganised 10 New Department consolidates Marine Science strengths 10 Notes and Reports Plant records Conservation status of titirangi (Hebe speciosa) 11 Senecio sterquilinus Ornduff in the Wellington Ecological District ....... 16 Trip reports Ecological Forum Excursion to South Patagonia and Tierra del Fuego (2) .... 17 Tangihua Fungal Foray, 20-24 May 1992 19 Biography/Bibliography Biographical Notes (6) Peter Goyen, an addition 20 Biographical Notes (7) Joshua Rutland 20 New Zealand Botanists and Fellowships of the Royal Society 22 Forthcoming Meetings/Conferences Lichen Techniques Workshop 22 Forthcoming Trips/Tours Seventh New Zealand Fungal Foray 22 Publications Checklist of New Zealand lichens 23 The mosses of New Zealand, special offer 24 Book review An illustrated guide to fungi on wood in New Zealand 25 Letters to the Editor New Zealand Botanical Society President: Dr Eric Godley Secretary/Treasurer: Anthony Wright Committee: Sarah Beadel, Ewen Cameron, Colin Webb, Carol West Address: New Zealand Botanical Society C/- Auckland Institute & Museum Private Bag 92018 AUCKLAND Subscriptions The 1992 ordinary and institutional subs are $14 (reduced to $10 if paid by the due date on the subscription invoice). The 1992 student sub, available to full-time students, is $7 (reduced to $5 if paid by the due date on the subscription invoice). -
10 Seed Release and Dispersal Mechanisms
10 Seed Release and Dispersal Mechanisms For seedling recruitment to occur seeds need to be dispersed into an environment that promotes germination and seedling survival. Dispersal consists of two phases. Primary dispersal is defined as the initial transport of seeds or seed-bearing fruits (collectively seeds and fruits are called diaspores) to the ground or water body, or for aerial parasites, a host branch. Secondary dispersal relates to any subsequent movement to the seed’s final resting place. Primary dispersal may be active (e.g. seeds released explosively from the fruit, e.g. dehiscence (opening) of Hardenbergia pods), passive (e.g. seeds fall out when the capsules of Eucalyptus open), or require a vector to aid in seed removal (e.g. wind uplift of winged seeds of Hakea or winged fruits of Nuytsia; Amyema berries consumed by mistletoe birds). Secondary dispersal involves either a biotic (e.g. ants) or environmental (e.g. wind, water) vector, and it is usually a different mechanism than that involved in primary dispersal. While primary dispersal is usually only for a few metres, secondary dispersal may cover several kilometres, and sometimes thousands for tiny seeds. This chapter covers some of the dispersal mechanisms exhibited by the SouthWest flora following their release. Terminology used to describe seed dispersal mechanisms is provided in Table 10.1. Table 10.1: Seed dispersal terminology. Term Definition Anemochory Wind dispersed Chamaechory Dispersal by rolling along the ground (wind assisted) Zoochory Animal dispersed (general) Myrmecochory Ant dispersed Ornithochory Bird dispersed Mammalochory Mammal dispersed Hydrochory Water dispersed Barochory Unassisted (gravity causes seeds to drop to the ground) Autochory Dispersal assisted by the actions of the parent plant (e.g. -
Vegetaton and Flora of Lot 9503 Wedgetail Circle Parkerville
VEGETATON AND FLORA OF LOT 9503 WEDGETAIL CIRCLE PARKERVILLE Prepared for: COTERRA ENVIRONMENT 19/336 Churchill Avenue, SUBIACO WA 6008 Prepared by: Bennett Environmental Consulting Pty Ltd Sollya heterophylla PO Box 341 KALAMUNDA 6926 December 2012 STATEMENT OF LIMITATIONS Scope of Services This report (“the report”) has been prepared in accordance with the scope of services set out in the contract, or as otherwise agreed, between the Client and Eleanor Bennett (“the Author”). In some circumstances a range of factors such as time, budget, access and/or site disturbance constraints may have limited the scope of services. Reliance on Data In preparing the report, the Author has relied upon data, surveys, analyses, designs, plans and other information provided by the Client and other individuals and organisations, most of which are referred to in the report (“the data”). Except as otherwise stated in the report, the Author has not verified the accuracy or completeness of the data. To the extent that the statements, opinions, facts, information, conclusions and/or recommendations in the report (“conclusions”) are based in whole or part on the data, those conclusions are contingent upon the accuracy and completeness of the data. The Author will not be liable in relation to incorrect conclusions should any data, information or condition be incorrect or have been concealed, withheld, misrepresented or otherwise not fully disclosed to the Author. Environmental Conclusions In accordance with the scope of services, the Author has relied upon the data and has conducted environmental field monitoring and/or testing in the preparation of the report. The nature and extent of monitoring and/or testing conducted is described in the report. -
GENOME EVOLUTION in MONOCOTS a Dissertation
GENOME EVOLUTION IN MONOCOTS A Dissertation Presented to The Faculty of the Graduate School At the University of Missouri In Partial Fulfillment Of the Requirements for the Degree Doctor of Philosophy By Kate L. Hertweck Dr. J. Chris Pires, Dissertation Advisor JULY 2011 The undersigned, appointed by the dean of the Graduate School, have examined the dissertation entitled GENOME EVOLUTION IN MONOCOTS Presented by Kate L. Hertweck A candidate for the degree of Doctor of Philosophy And hereby certify that, in their opinion, it is worthy of acceptance. Dr. J. Chris Pires Dr. Lori Eggert Dr. Candace Galen Dr. Rose‐Marie Muzika ACKNOWLEDGEMENTS I am indebted to many people for their assistance during the course of my graduate education. I would not have derived such a keen understanding of the learning process without the tutelage of Dr. Sandi Abell. Members of the Pires lab provided prolific support in improving lab techniques, computational analysis, greenhouse maintenance, and writing support. Team Monocot, including Dr. Mike Kinney, Dr. Roxi Steele, and Erica Wheeler were particularly helpful, but other lab members working on Brassicaceae (Dr. Zhiyong Xiong, Dr. Maqsood Rehman, Pat Edger, Tatiana Arias, Dustin Mayfield) all provided vital support as well. I am also grateful for the support of a high school student, Cady Anderson, and an undergraduate, Tori Docktor, for their assistance in laboratory procedures. Many people, scientist and otherwise, helped with field collections: Dr. Travis Columbus, Hester Bell, Doug and Judy McGoon, Julie Ketner, Katy Klymus, and William Alexander. Many thanks to Barb Sonderman for taking care of my greenhouse collection of many odd plants brought back from the field. -
Vicariance, Climate Change, Anatomy and Phylogeny of Restionaceae
Botanical Journal of the Linnean Society (2000), 134: 159–177. With 12 figures doi:10.1006/bojl.2000.0368, available online at http://www.idealibrary.com on Under the microscope: plant anatomy and systematics. Edited by P. J. Rudall and P. Gasson Vicariance, climate change, anatomy and phylogeny of Restionaceae H. P. LINDER FLS Bolus Herbarium, University of Cape Town, Rondebosch 7701, South Africa Cutler suggested almost 30 years ago that there was convergent evolution between African and Australian Restionaceae in the distinctive culm anatomical features of Restionaceae. This was based on his interpretation of the homologies of the anatomical features, and these are here tested against a ‘supertree’ phylogeny, based on three separate phylogenies. The first is based on morphology and includes all genera; the other two are based on molecular sequences from the chloroplast genome; one covers the African genera, and the other the Australian genera. This analysis corroborates Cutler’s interpretation of convergent evolution between African and Australian Restionaceae. However, it indicates that for the Australian genera, the evolutionary pathway of the culm anatomy is much more complex than originally thought. In the most likely scenario, the ancestral Restionaceae have protective cells derived from the chlorenchyma. These persist in African Restionaceae, but are soon lost in Australian Restionaceae. Pillar cells and sclerenchyma ribs evolve early in the diversification of Australian Restionaceae, but are secondarily lost numerous times. In some of the reduction cases, the result is a very simple culm anatomy, which Cutler had interpreted as a primitively simple culm type, while in other cases it appears as if the functions of the ribs and pillars may have been taken over by a new structure, protective cells developed from epidermal, rather than chlorenchyma, cells. -
Jan Dvorak (As Quickly Written Down by a Person with Poor Hearing…Me)
1/22/2018 The Impact of Polyploidy on Genome Evolution in Poales and Other Monocots “I don’t have to emphasize that gene duplications are the fabric of evolution in plants.” -Jan Dvorak (as quickly written down by a person with poor hearing…me) Michael R. McKain The University of Alabama @mrmckain @mrmckain Poales Diversity Grass genomes: the choose your own adventure of genome evolution • ~22,800 species • ~11,088 species in Poaceae • Transposons (McClintock, Wessler) • GC content bias (Carels and Bernardi 2000) • Three WGD events 0 0 4 0 0 • rho (Peterson et al. 2004) 3 y c n 0 e 0 u 2 q e r F • 0 sigma (Tang et al. 2010) 0 1 • tau (Tang et al. 2010, Jiao et al. 2014) 0 %GC Givnish et al. 2010 @mrmckain Schnable et al., 2009 Zeroing in on WGD placement Banana genome Pineapple genome How has ancient polyploidy altered the genomic landscape in grasses and other Poales? D’Hont et al. 2012 Ming, VanBuren et al. 2015 Recovered sigma after grass divergence from commelinids Recovered sigma after grass+pineapple divergence from commelinids @mrmckain @mrmckain 1 1/22/2018 Phylotranscriptomic approach Coalescence-based Phylogeny of 234 Single-copy genes • Sampling 27 transcriptomes and 7 genomes • Phylogeny consistent with previous • Representation for all families (except Thurniaceae) in nuclear gene results Poales • Conflicting topology with • RNA from young leaf or apical meristem, a combination of chloroplast genome tree: Moncot Tree of Life and 1KP • Ecdeiocolea/Joinvillea sister instead of • General steps: a grade • Trinity assembly • Typha