Seed-Set in Some Native Legumes
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Apoidea (Insecta: Hymenoptera). Fauna of New Zealand 57, 295 Pp. Donovan, B. J. 2007
Donovan, B. J. 2007: Apoidea (Insecta: Hymenoptera). Fauna of New Zealand 57, 295 pp. EDITORIAL BOARD REPRESENTATIVES OF L ANDCARE R ESEARCH Dr D. Choquenot Landcare Research Private Bag 92170, Auckland, New Zealand Dr R. J. B. Hoare Landcare Research Private Bag 92170, Auckland, New Zealand REPRESENTATIVE OF UNIVERSITIES Dr R.M. Emberson c/- Bio-Protection and Ecology Division P.O. Box 84, Lincoln University, New Zealand REPRESENTATIVE OF M USEUMS Mr R.L. Palma Natural Environment Department Museum of New Zealand Te Papa Tongarewa P.O. Box 467, Wellington, New Zealand REPRESENTATIVE OF OVERSEAS I NSTITUTIONS Dr M. J. Fletcher Director of the Collections NSW Agricultural Scientific Collections Unit Forest Road, Orange NSW 2800, Australia * * * SERIES EDITOR Dr T. K. Crosby Landcare Research Private Bag 92170, Auckland, New Zealand Fauna of New Zealand Ko te Aitanga Pepeke o Aotearoa Number / Nama 57 Apoidea (Insecta: Hymenoptera) B. J. Donovan Donovan Scientific Insect Research, Canterbury Agriculture and Science Centre, Lincoln, New Zealand [email protected] Manaaki W h e n u a P R E S S Lincoln, Canterbury, New Zealand 2007 4 Donovan (2007): Apoidea (Insecta: Hymenoptera) Copyright © Landcare Research New Zealand Ltd 2007 No part of this work covered by copyright may be reproduced or copied in any form or by any means (graphic, electronic, or mechanical, including photocopying, recording, taping information retrieval systems, or otherwise) without the written permission of the publisher. Cataloguing in publication Donovan, B. J. (Barry James), 1941– Apoidea (Insecta: Hymenoptera) / B. J. Donovan – Lincoln, N.Z. : Manaaki Whenua Press, Landcare Research, 2007. (Fauna of New Zealand, ISSN 0111–5383 ; no. -
A Molecular Phylogenetic Perspective
Astragalus (Fabaceae): A molecular phylogenetic perspective MARTIN F. WOJCIECHOWSKI Wojciechowski, M. E (School of Life Sciences, Arizona State University, Tem- pe, AZ, 85287-4501, U.S.A.; e-mail: [email protected]). Astragalus (Fa- baceae): A molecular phylogenetic perspective. Brittonia 57: 382-396. 2005.-- Nucleotide sequences of the plastid mark gene and nuclear rDNA internal tran- scribed spacer region were sampled from Astragalus L. (Fabaceae), and its closest relatives within tribe Galegeae, to infer phylogenetic relationships and estimate ages of diversification. Consistent with previous studies that emphasized sampling for nrDNA ITS primarily within either New World or Old World species groups, Astragalus, with the exception of a few morphologically distinct species, is strongly supported as monophyletic based on maximum parsimony and Bayesian analyses of matK sequences as well as a combined sequence dataset. The matK data provides better resolution and stronger clade support for relationships among Astragalus and traditionally related genera than nrDNA ITS. Astragalus sensu stricto plus the genus Oxytropis are strongly supported as sister to a clade com- posed of strictly Old World (African, Australasian) genera such as Colutea, Suth- erlandia, Lessertia, Swainsona, and Carrnichaelia, plus several morphologically distinct segregates of Eurasian Astragalus. Ages of these clades and rates of nucleotide substitution estimated from a fossil-constrained, rate-smoothed, Bayes- ian analysis of matK sequences sampled from Hologalegina indicate Astragalus diverged from its sister group, Oxytropis, 12-16 Ma, with divergence of Neo- Astragalus beginning ca. 4.4 Ma. Estimates of absolute rates of nucleotide sub- stitution for Astragalus and sister groups, which range from 8.9 to 10.2 x 10 -~0 substitutions per site per year, are not unusual when compared to those estimated for other, mainly temperate groups of papilionoid legumes. -
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Liversidge Research Lecture No. 6 1946 PLANT PRODUCTS OF NEW ZEALAND LINDSAY H. BRIGGS The Royal Society of New South Wales Liversidge Research Lecture No. 6, 1946 Royal Society of NSW 1 Lindsay Heathcote Briggs This photograph is reproduced from Proceedings of the Royal Society of New Zealand, 1974-5, 103, pp. 100-110, by permission of the Royal Society of New Zealand, and SIR Publishing, Wellington, New Zealand 162 2 Royal Society of NSW Liversidge Research Lecture No. 6, 1946 Liversidge Research Lecturer No. 6, 1946 LINDSAY HEATHCOTE BRIGGS 1905-1975 Lindsay Heathcote Briggs was born on 3 January 1905 in Hastings, New Zealand. His secondary education was at Hastings District High School where he was Dux in 1919 and 1920, and was awarded a Senior National Scholarship in 1919; from 1921 to 1923 he attended Auckland Grammar School where he won a Williamson Scholarship in 1922 and a University Entrance Scholarship in 1923. He then studied science at Auckland University, winning a Sir George Grey Scholarship in 1926, and graduated M.Sc. with Honours in 1928 while holding a Duffus Lubecki Research Scholarship. In 1929 he was awarded a New Zealand National Research Scholarship, but he relinquished this to take up a Sir James Gunson Scholarship for research in Dairy Science at Massey Agricultural College. In 1931 he proceeded to Oxford where he worked under Professor (later Sir) Robert Robinson; he was awarded an Oxford Exhibition Scholarship of the British Association for the Advancement of Science, and in 1933 he graduated D.Phil. with a thesis entitled "The Molecular Structure of Strychnine". -
Bio 308-Course Guide
COURSE GUIDE BIO 308 BIOGEOGRAPHY Course Team Dr. Kelechi L. Njoku (Course Developer/Writer) Professor A. Adebanjo (Programme Leader)- NOUN Abiodun E. Adams (Course Coordinator)-NOUN NATIONAL OPEN UNIVERSITY OF NIGERIA BIO 308 COURSE GUIDE National Open University of Nigeria Headquarters 14/16 Ahmadu Bello Way Victoria Island Lagos Abuja Office No. 5 Dar es Salaam Street Off Aminu Kano Crescent Wuse II, Abuja e-mail: [email protected] URL: www.nou.edu.ng Published by National Open University of Nigeria Printed 2013 ISBN: 978-058-434-X All Rights Reserved Printed by: ii BIO 308 COURSE GUIDE CONTENTS PAGE Introduction ……………………………………......................... iv What you will Learn from this Course …………………............ iv Course Aims ……………………………………………............ iv Course Objectives …………………………………………....... iv Working through this Course …………………………….......... v Course Materials ………………………………………….......... v Study Units ………………………………………………......... v Textbooks and References ………………………………........... vi Assessment ……………………………………………….......... vi End of Course Examination and Grading..................................... vi Course Marking Scheme................................................................ vii Presentation Schedule.................................................................... vii Tutor-Marked Assignment ……………………………….......... vii Tutors and Tutorials....................................................................... viii iii BIO 308 COURSE GUIDE INTRODUCTION BIO 308: Biogeography is a one-semester, 2 credit- hour course in Biology. It is a 300 level, second semester undergraduate course offered to students admitted in the School of Science and Technology, School of Education who are offering Biology or related programmes. The course guide tells you briefly what the course is all about, what course materials you will be using and how you can work your way through these materials. It gives you some guidance on your Tutor- Marked Assignments. There are Self-Assessment Exercises within the body of a unit and/or at the end of each unit. -
Swainsona Murrayana
Swainsona murrayana VU Taxonomic Authority: Wawra Global Assessment Regional Assessment Region: Global Endemic to region Synonyms Common Names Swainsona morrisian J.M.Black SLENDER DARLING-PEA English (Primary) Swainsona murrayan A.T.Lee MURRAY SWAINSON-PE English SLENDER SWAINSON English Upper Level Taxonomy Kingdom: PLANTAE Phylum: TRACHEOPHYTA Class: MAGNOLIOPSIDA Order: FABALES Family: LEGUMINOSAE Lower Level Taxonomy Rank: Infra- rank name: Plant Hybrid Subpopulation: Authority: General Information Distribution Swainsona murrayana is endemic to Australia, distributed on the western slopes and plains of New South Wales and in equivalent areas of northern and western Victoria and southern Queensland, and with an outlying population in South Australia west of Broken Hill (Thompson 1993). Range Size Elevation Biogeographic Realm Area of Occupancy: Upper limit: 450 Afrotropical Extent of Occurrence: Lower limit: 60 Antarctic Map Status: Depth Australasian Upper limit: Neotropical Lower limit: Oceanian Depth Zones Palearctic Shallow photic Bathyl Hadal Indomalayan Photic Abyssal Nearctic Population Total population size is not known. A recent survey suggests ~100 mature individuals in a population in South Australia population (MSBP 2010). In Victoria there are 28 known populations with a total with a total of 94,000 individuals occupaying 164 hectares (DSE 2003). In New South Wales, this species has been recorded in 23 separate plant communities, 16 of which have been classified as threatened, with most communities having experienced more than 50% decline and 13 communities still experiencing continuing decline (Benson 2006). Total Population Size Minimum Population Size: Maximum Population Size: Habitat and Ecology This herb often grows on heavy soils, especially in depressions associated with chenopod shrubs (Maireana spp.), wallaby-grass (Austrodanthonia spp.), and spear grass (Austrostipa spp.). -
Fruits and Seeds of Genera in the Subfamily Faboideae (Fabaceae)
Fruits and Seeds of United States Department of Genera in the Subfamily Agriculture Agricultural Faboideae (Fabaceae) Research Service Technical Bulletin Number 1890 Volume I December 2003 United States Department of Agriculture Fruits and Seeds of Agricultural Research Genera in the Subfamily Service Technical Bulletin Faboideae (Fabaceae) Number 1890 Volume I Joseph H. Kirkbride, Jr., Charles R. Gunn, and Anna L. Weitzman Fruits of A, Centrolobium paraense E.L.R. Tulasne. B, Laburnum anagyroides F.K. Medikus. C, Adesmia boronoides J.D. Hooker. D, Hippocrepis comosa, C. Linnaeus. E, Campylotropis macrocarpa (A.A. von Bunge) A. Rehder. F, Mucuna urens (C. Linnaeus) F.K. Medikus. G, Phaseolus polystachios (C. Linnaeus) N.L. Britton, E.E. Stern, & F. Poggenburg. H, Medicago orbicularis (C. Linnaeus) B. Bartalini. I, Riedeliella graciliflora H.A.T. Harms. J, Medicago arabica (C. Linnaeus) W. Hudson. Kirkbride is a research botanist, U.S. Department of Agriculture, Agricultural Research Service, Systematic Botany and Mycology Laboratory, BARC West Room 304, Building 011A, Beltsville, MD, 20705-2350 (email = [email protected]). Gunn is a botanist (retired) from Brevard, NC (email = [email protected]). Weitzman is a botanist with the Smithsonian Institution, Department of Botany, Washington, DC. Abstract Kirkbride, Joseph H., Jr., Charles R. Gunn, and Anna L radicle junction, Crotalarieae, cuticle, Cytiseae, Weitzman. 2003. Fruits and seeds of genera in the subfamily Dalbergieae, Daleeae, dehiscence, DELTA, Desmodieae, Faboideae (Fabaceae). U. S. Department of Agriculture, Dipteryxeae, distribution, embryo, embryonic axis, en- Technical Bulletin No. 1890, 1,212 pp. docarp, endosperm, epicarp, epicotyl, Euchresteae, Fabeae, fracture line, follicle, funiculus, Galegeae, Genisteae, Technical identification of fruits and seeds of the economi- gynophore, halo, Hedysareae, hilar groove, hilar groove cally important legume plant family (Fabaceae or lips, hilum, Hypocalypteae, hypocotyl, indehiscent, Leguminosae) is often required of U.S. -
Montigena Novae-Zelandiae
Montigena novae-zelandiae COMMON NAME Scree pea SYNONYMS Swainsona novae-zelandiae Hook.f. var. novae-zelandiae, Swainsona novae-zelandiae var. glabra G.Simpson FAMILY Fabaceae AUTHORITY Montigena novae-zelandiaev (Hook.f.) Heenan FLORA CATEGORY Vascular – Native ENDEMIC TAXON Yes ENDEMIC GENUS Hawkdun Range. Photographer: John Barkla Yes ENDEMIC FAMILY No STRUCTURAL CLASS Herbs - Dicotyledons other than Composites NVS CODE MONNOV CHROMOSOME NUMBER Close up of Montigena. Photographer: Shannel 2n = 32 Courtney CURRENT CONSERVATION STATUS 2012 | At Risk – Declining | Qualifiers: RF, Sp PREVIOUS CONSERVATION STATUSES 2009 | At Risk – Declining | Qualifiers: RF, Sp 2004 | Gradual Decline DISTRIBUTION South Island, east of Southern Alps. HABITAT Subalpine to low alpine, on fine-grained, partially stable and moist greywacke scree, rock debris and gravel slopes. Sometimes in depleted tussock grasslands. FEATURES Small woody sub-shrub arising from thin, branched stems that extend to the surface from a deeply buried root stock. Foliage a dull green, leafy tufts, 30-70mm long, 10-60mm wide. Leaves divided, 20-35mm long. Leaflets in 6-10 pairs per leaf, usually folded along the mid-rib; fleshy, grey-green or grey-blue and sometimes flushed red. Flowers in bunches, purplish, clover-pink or golden-brown, arising from axils of older leaves. Seed pods swollen, darkening to orange-red at maturity, grey brown when open. Seeds 10 per pod, 3.5mm long, 3mm wide, brown. SIMILAR TAXA None. Large bloated sausage-shaped seed pods, fern-like leaf form. FLOWERING December - February FLOWER COLOURS Red/Pink, Violet/Purple FRUITING January - April PROPAGATION TECHNIQUE Difficult and should not be removed from the wild. -
Dessication Response of Seed of Clianthus Spp., Carmichaelia Muritai, Pittosporum Crassifolium and Pittosporum Eugenoides
Copyright is owned by the Author of the thesis. Permission is given for a copy to be downloaded by an individual for the purpose of research and private study only. The thesis may not be reproduced elsewhere without the permission of the Author. Desiccation response of seed of Clianthus spp., Carmichaelia muritai, Pittosporum crassifolium and Pittosporum eugenioides A thesis presented in partial fulfilment of the requirements for the degree of Master of AgriScience in Horticulture at Massey University, Palmerston North, New Zealand Kai Yu 2015 ABSTRACT New Zealand has a rich, diverse and unique of plant life. However, the conservation status of the New Zealand indigenous vascular flora is deteriorating, with 7.6% of this flora regarded as threatened with extinction. A series of conservation approaches are required to protect species against further loss. Developing ex-situ conservation of these species requires basic information such as seed storage behaviour and seed germination requirements to be determined. However, for many species this information is missing or incomplete. The objective of this study was to determine seed storage behaviour (response to desiccation), and/or seed coat characteristics in selected New Zealand native species. Five native tree and shrub species were studied: Carmichaelia muritai, Clianthus puniceus, Clianthus maximus, Pittosporum eugenioides, and Pittosporum crassifolium. Seeds of Clianthus maximus, Clianthus puniceus, and Carmichaelia muritai were found desiccation tolerant at low moisture content (down to ~2.5%), suggesting the storage behaviour is orthodox; storage trials need to be conducted to confirm this. In contrast, the storage behaviour of Pittosporum eugenioides and Pittosporum crassifolium appears to be non-orthodox since there was some loss of viability upon drying to low moisture contents. -
Native Plant Identification CONTACT in the Northern and Yorke Region
Government of South Australia Northern and Yorke Natural FACT SHEET NO 2.018 Resources Management Board September 2011 NRM Plan Native plant identification CONTACT In the Northern and Yorke Region Main Office Basic plant identification is a vital skill for Northern and Yorke NRM Board land managers. It assists in appreciating PO Box 175 the vegetation around you and managing 41-49 Eyre Road that vegetation. Does a plant belong on a Crystal Brook SA 5523 site or is it a weed? Ph: (08) 8636 2361 Fx: (08) 8636 2371 This fact sheet introduces some of the www.nynrm.sa.gov.au common plant groups of the Northern and Yorke Region and how to identify them. All living things have been categorized into what is known as the Linnaean System of classification. Plants are grouped using common attributes until each plant is given a unique Classification. The steps of Classification are: • Kingdom • Division • Class • Order • Family • Subfamily • Genus • Species This results in a unique Botanical or Scientific name consisting of Genus and Species. Some plants are further split into sub species. Most plants have at least one common name. These are non scientific and often vary from region to region. Some plants may have the same common name, this often causes confusion so it is important to use the Botanical name. The plants right would be referred to as Eucalyptus leucoxylon subspecies leucoxylon or the South Australian Blue Gum. This plant is known as Yellow Gum in Victoria. Glossary of common botanical terms Annual A plant that completes its life within one year. -
Peas (Swainsona Species)
Action Statement Flora and Fauna Guarantee Act 1988 No. 126 Twelve threatened Swainson-peas and Darling- peas (Swainsona species) Description and distribution The genus Swainsona is represented in Victoria by Distribution maps of each species can be found at 18 species, of which all but four are considered to the end of this Action Statement. be threatened in the wild. This Action Statement Habitat addresses 12 threatened (vulnerable or endangered) taxa of Swainsona listed below. Swainsona species are confined to specific Detailed survey and monitoring of all known grassland and woodland habitats found in south- populations was undertaken between September west Victoria, the Mallee, native grasslands of the 1997 and September 1999. The information northern plains, and riverine habitats along the presented in this Action Statement is based on Murray River. results of these surveys which are stored on the Department of Sustainability and Environment Life history and ecology threatened plant population monitoring database, Swainsona species are largely renascent perennials, VROTPop. Of the two remaining threatened resprouting in suitable conditions from a Swainsona species, Swainsona galegifolia already persistent rootstock. This gives individual plants has a published Action Statement, while Swainsona the capacity to persist between years given suitable recta is presumed extinct in Victoria. conditions. Walsh et al. (1996) also comment that Swainsona species are small to medium annuals or Swainsona purpurea can behave as an annual. renascent perennials, with hairy to glabrous, Growth and flowering among most species of pinnate foliage with 3 - 7 linear leaflets, and Swainsona species appears to be stimulated by flowers arranged in racemes (on lateral stalks) available moisture, thus plants are most frequently varying from yellow to red, pink, purple or violet in observable following adequate Spring rainfall. -
The Island Rule and Its Application to Multiple Plant Traits
The island rule and its application to multiple plant traits Annemieke Lona Hedi Hendriks A thesis submitted to the Victoria University of Wellington in partial fulfilment of the requirements for the degree of Master of Science in Ecology and Biodiversity Victoria University of Wellington, New Zealand 2019 ii “The larger the island of knowledge, the longer the shoreline of wonder” Ralph W. Sockman. iii iv General Abstract Aim The Island Rule refers to a continuum of body size changes where large mainland species evolve to become smaller and small species evolve to become larger on islands. Previous work focuses almost solely on animals, with virtually no previous tests of its predictions on plants. I tested for (1) reduced floral size diversity on islands, a logical corollary of the island rule and (2) evidence of the Island Rule in plant stature, leaf size and petiole length. Location Small islands surrounding New Zealand; Antipodes, Auckland, Bounty, Campbell, Chatham, Kermadec, Lord Howe, Macquarie, Norfolk, Snares, Stewart and the Three Kings. Methods I compared the morphology of 65 island endemics and their closest ‘mainland’ relative. Species pairs were identified. Differences between archipelagos located at various latitudes were also assessed. Results Floral sizes were reduced on islands relative to the ‘mainland’, consistent with predictions of the Island Rule. Plant stature, leaf size and petiole length conformed to the Island Rule, with smaller plants increasing in size, and larger plants decreasing in size. Main conclusions Results indicate that the conceptual umbrella of the Island Rule can be expanded to plants, accelerating understanding of how plant traits evolve on isolated islands. -
Carmichaelia Torulosa
Carmichaelia torulosa COMMON NAME Canterbury Pink Broom SYNONYMS Notospartium torulosum Kirk FAMILY Fabaceae AUTHORITY Carmichaelia torulosa (Kirk) Heenan FLORA CATEGORY Vascular – Native ENDEMIC TAXON Yes ENDEMIC GENUS No Snowdon Station, Canterbury. Photographer: Roy Veronese ENDEMIC FAMILY No STRUCTURAL CLASS Trees & Shrubs - Dicotyledons NVS CODE CARTOR CHROMOSOME NUMBER 2n = 32 CURRENT CONSERVATION STATUS Washpen Creek, Malvern Hills (January). 2018 | Threatened – Nationally Critical Photographer: John Smith-Dodsworth PREVIOUS CONSERVATION STATUSES 2012 | Threatened – Nationally Endangered | Qualifiers: DP, RF 2009 | Threatened – Nationally Endangered | Qualifiers: DP, RF 2004 | Range Restricted BRIEF DESCRIPTION Rare small tree or large shrub with erect leafless twigs inhabiting inland Canterbury. Trunk very short. Twigs 1.2-2.5mm wide, rounded. Flowers lavender-pink with darker veins. Fruit a dry pod containing up to 15 hard seeds and which widens where a seed is present giving a distinctive horizontally ribbed appearance. DISTRIBUTION Endemic. New Zealand: South Island (Canterbury (Amuri Range (North Canterbury) to Te Ngawai River (South Canterbury)) HABITAT A plant of forest margins, especially riparian shrubland and low forest, and on rock bluffs. It has also been found within a wetland. Plants grow in a range of vegetation types from grassland and open shrubland to closed shrubland and low forest, though it is most commonly an emergent within open to dense shrubland. FEATURES Shrub or small tree up to 5 m tall. Trunk slender, brittle, usually branching close to base; branches slender, suberect to erect, leafless, initially red-green maturing grey to grey-green; branchlets numerous, suberect to erect, terete, dark green, 1.2-2.5 mm diameter. Inflorescences racemose, 1(-2) per node, up to c.50 mm long, slender, 1-10 flowered, flowers not crowded.