Stackhousia Subterranea (Grassland Candles) Grassland Candles
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Approved Conservation Advice for Stackhousia Annua (Annual Stackhousia)
This Conservation Advice was approved by the Minister / Delegate of the Minister on: 1/10/2008 Approved Conservation Advice (s266B of the Environment Protection and Biodiversity Conservation Act 1999) Approved Conservation Advice for Stackhousia annua (Annual Stackhousia) This Conservation Advice has been developed based on the best available information at the time this conservation advice was approved; this includes existing plans, records or management prescriptions for this species. Description Stackhousia annua, Family Stackhousiaceae, also known as Annual Stackhousia or Annual Candles, is a slender, erect, hairless annual growing to 19 cm (Barker, 1984). Leaves are 7– 25 mm long; basal leaves are narrowly spatulate and upper leaves are obovate (egg-shaped) to linear. Flowering occurs from September to October. The cream coloured flowers grow at the ends of stems in a dense, cylindrical floral spike (State Herbarium of South Australia, 2007). Conservation Status Annual Stackhousia is listed as vulnerable. This species is eligible for listing as vulnerable under the Environment Protection and Biodiversity Conservation Act 1999 (Cwlth) (EPBC Act) as, prior to the commencement of the EPBC Act, it was listed as vulnerable under Schedule 1 of the Endangered Species Protection Act 1992 (Cwlth). This species is also listed as vulnerable on the National Parks and Wildlife Act 1972 (South Australia). Distribution and Habitat Annual Stackhousia is endemic to near-coastal areas of south-west Yorke Peninsula and south-east Eyre Peninsula, South Australia (Barker, 1977; Barker, 1984; Pobke, 2007). This species was thought to occur in north-west Victoria and the South Australian mallee region (Walsh & Entwisle, 1999), but these records are now called a subspecies of Stackhousia aspericocca (Ross & Walsh, 2003). -
CANDOLLE, Prodr., XV, (1864)
The Genus Stackhousia in the Malay Archipelago by F.I. Brouwer (Botanical Laboratory of the University, Groningen, Netherlands). This publication is based on herbarium, materials which were kindly placed at the author’s disposal by the Directors of the Herbarium of the Buitenzorg Botanic Garden (B), the Leiden National Herbarium (L), the Herbarium of the Utrecht University (U), and the Herbarium of the Berlin-Dahlem Botanical Museum (BD), for whose kind help the author wishes to render his best thanks. Stackhousia SMITH, in Transact. Linn. Soc. London, IV (1798) 298. Most important literature: BENTHAM & HOOKER FIL., Gen. pi., I, 1 (1862) 371; BENTILAM, PL austr., I (1863) 404; in DE CANDOLLE, Prodr., XV, 1 (1864) 499; PAX, in ENGL. & PR., Nat. Pflanzenfam., ILL, 5 (1896) 233; BAILEY, Queensl. PL, I (1899) 263; PAMPANINI, in Bull. Herb. Boiss., ser. 2, V (1905) 912; VI (1906) tab. 13. Flowers regular, hermaphrodite. Calyx 5-merous, sepals usually more or less connate, rarely free. Corolla 5-merous, perigynous or nearly hypogynous; petals with long claws, rarely entirely free, usually free in the lower portion, connate in the upper portion of the claws; lobes 5, spreading, imbricate. Stamens 5, inserted on the margin of the calyx tube, free, usually different in length, included in the corolla tube. Ovary 2—5-, but usually 3-celled, each cell with one erect ana- tropous ovule; style with 2—5, usually 3, stigmatic lobes. Fruit with seed with 2—5, usually 3, one-seeded cocci and a central columella; membranous testa, fleshy albumen, straight embryo, short cotyledons, and inferior radicle. -
First Steps Towards a Floral Structural Characterization of the Major Rosid Subclades
Zurich Open Repository and Archive University of Zurich Main Library Strickhofstrasse 39 CH-8057 Zurich www.zora.uzh.ch Year: 2006 First steps towards a floral structural characterization of the major rosid subclades Endress, P K ; Matthews, M L Abstract: A survey of our own comparative studies on several larger clades of rosids and over 1400 original publications on rosid flowers shows that floral structural features support to various degrees the supraordinal relationships in rosids proposed by molecular phylogenetic studies. However, as many apparent relationships are not yet well resolved, the structural support also remains tentative. Some of the features that turned out to be of interest in the present study had not previously been considered in earlier supraordinal studies. The strongest floral structural support is for malvids (Brassicales, Malvales, Sapindales), which reflects the strong support of phylogenetic analyses. Somewhat less structurally supported are the COM (Celastrales, Oxalidales, Malpighiales) and the nitrogen-fixing (Cucurbitales, Fagales, Fabales, Rosales) clades of fabids, which are both also only weakly supported in phylogenetic analyses. The sister pairs, Cucurbitales plus Fagales, and Malvales plus Sapindales, are structurally only weakly supported, and for the entire fabids there is no clear support by the present floral structural data. However, an additional grouping, the COM clade plus malvids, shares some interesting features but does not appear as a clade in phylogenetic analyses. Thus it appears that the deepest split within eurosids- that between fabids and malvids - in molecular phylogenetic analyses (however weakly supported) is not matched by the present structural data. Features of ovules including thickness of integuments, thickness of nucellus, and degree of ovular curvature, appear to be especially interesting for higher level relationships and should be further explored. -
Taxonomic and Phylogenetic Census of the Celastrales: a Synthetic Review Shisode S.B.1 and D.A
Curr. Bot. 2(4): 36-43, 2011 REVIEW ARTICLE Taxonomic and phylogenetic census of the Celastrales: A synthetic review Shisode S.B.1 and D.A. Patil2 1 Department of Botany L. V. H. College, Panchavati, Nashik–422003 (M.S.) India 2 Post-Graduate Department of Botany S.S.V.P. Sanstha’s L.K.Dr.P.R.Ghogrey Science College, Dhule – 424 005, India K EYWORDS A BSTRACT Taxonomy, Phylogeny, Celastrales A comprehensive assessment of the taxonomic and phylogenetic status of the celeastralean plexus is presented. An attempt has been made to review synthetically C ORRESPONDENCE based on the data from different disciplines divulged by earlier authors and from present author’s study on the alliance. The taxonomic literature indicated that the D.A. Patil, Post-Graduate Department of Botany Celeastrales (sensu lato) are a loose-knit assemblage. The tribal, subfamilial, familial S.S.V.P. Sanstha’s L.K.Dr.P.R.Ghogrey Science and even ordinal boundaries are uncertain and even criss-cross each other. It College , Dhule – 424 005, India appeared that the alliance can be grouped under two taxonomic entities viz., the Celastrales and the Rhamnales which appear evolved convergently. E-mail: [email protected] E DITOR Datta Dhale CB Volume 2, Year 2011, Pages 36-43 Introduction Hipporcrateaceae are accorded an independent familial status. The order Celastrales (sensu lato) is a loose - knit The family Rhamnaceae is included under the Rhamnales assemblage. The taxonomic history clearly reflected that this alongwith the Vitaceae only. In the latest Engler's syllabus, alliance is not restricted to any taxonomic entity. -
On the Flora of Australia
L'IBRARY'OF THE GRAY HERBARIUM HARVARD UNIVERSITY. BOUGHT. THE FLORA OF AUSTRALIA, ITS ORIGIN, AFFINITIES, AND DISTRIBUTION; BEING AN TO THE FLORA OF TASMANIA. BY JOSEPH DALTON HOOKER, M.D., F.R.S., L.S., & G.S.; LATE BOTANIST TO THE ANTARCTIC EXPEDITION. LONDON : LOVELL REEVE, HENRIETTA STREET, COVENT GARDEN. r^/f'ORElGN&ENGLISH' <^ . 1859. i^\BOOKSELLERS^.- PR 2G 1.912 Gray Herbarium Harvard University ON THE FLORA OF AUSTRALIA ITS ORIGIN, AFFINITIES, AND DISTRIBUTION. I I / ON THE FLORA OF AUSTRALIA, ITS ORIGIN, AFFINITIES, AND DISTRIBUTION; BEIKG AN TO THE FLORA OF TASMANIA. BY JOSEPH DALTON HOOKER, M.D., F.R.S., L.S., & G.S.; LATE BOTANIST TO THE ANTARCTIC EXPEDITION. Reprinted from the JJotany of the Antarctic Expedition, Part III., Flora of Tasmania, Vol. I. LONDON : LOVELL REEVE, HENRIETTA STREET, COVENT GARDEN. 1859. PRINTED BY JOHN EDWARD TAYLOR, LITTLE QUEEN STREET, LINCOLN'S INN FIELDS. CONTENTS OF THE INTRODUCTORY ESSAY. § i. Preliminary Remarks. PAGE Sources of Information, published and unpublished, materials, collections, etc i Object of arranging them to discuss the Origin, Peculiarities, and Distribution of the Vegetation of Australia, and to regard them in relation to the views of Darwin and others, on the Creation of Species .... iii^ § 2. On the General Phenomena of Variation in the Vegetable Kingdom. All plants more or less variable ; rate, extent, and nature of variability ; differences of amount and degree in different natural groups of plants v Parallelism of features of variability in different groups of individuals (varieties, species, genera, etc.), and in wild and cultivated plants vii Variation a centrifugal force ; the tendency in the progeny of varieties being to depart further from their original types, not to revert to them viii Effects of cross-impregnation and hybridization ultimately favourable to permanence of specific character x Darwin's Theory of Natural Selection ; — its effects on variable organisms under varying conditions is to give a temporary stability to races, species, genera, etc xi § 3. -
John Stackhouse (1742-1819) and the Linnean Society
NEWSLETTER AND PROCEEDINGS OF THE LINNEAN SOCIETY OF LONDON VOLUME 24 • NUMBER 1 • JANUARY 2008 THE LINNEAN SOCIETY OF LONDON Registered Charity Number 220509 Burlington House, Piccadilly, London W1J 0BF Tel. (+44) (0)20 7434 4479; Fax: (+44) (0)20 7287 9364 e-mail: [email protected]; internet: www.linnean.org President Secretaries Council Professor David F Cutler BOTANICAL The Officers and Dr Sandra D Knapp Dr Pieter Baas Vice-Presidents Dr Andy Brown Professor Richard M Bateman ZOOLOGICAL Dr Joe Cain Dr Jenny M Edmonds Dr Vaughan R Southgate Dr John David Dr Sandy D Knapp Prof Peter S Davis Dr Vaughan R Southgate EDITORIAL Dr Shahina Ghazanfar Dr John R Edmondson Dr D J Nicholas Hind Treasurer Mr W M Alastair Land Professor Gren Ll Lucas OBE COLLECTIONS Dr D Tim J Littlewood Mrs Susan Gove Dr George McGavin Acting Executive Secretary Dr Malcolm Scoble Miss Gina Douglas Librarian & Archivist Prof Mark Seaward Miss Gina Douglas Dr Max Telford Head of Development Ms Elaine Shaughnessy Deputy Librarian Conservator Mrs Lynda Brooks Ms Janet Ashdown Financial Controller/Membership Mr Priya Nithianandan Assistant Librarian Special Publications Mr Ben Sherwood Manager Building and Office Manager Ms Leonie Berwick Ms Victoria Smith Communications Manager Ms Kate Longhurst THE LINNEAN Newsletter and Proceedings of the Linnean Society of London ISSN 0950-1096 Edited by Brian G Gardiner Editorial .......................................................................................................................2 Society News.............................................................................................................. -
BMC Evolutionary Biology Biomed Central
BMC Evolutionary Biology BioMed Central Research article Open Access Mitochondrial matR sequences help to resolve deep phylogenetic relationships in rosids Xin-Yu Zhu1,2, Mark W Chase3, Yin-Long Qiu4, Hong-Zhi Kong1, David L Dilcher5, Jian-Hua Li6 and Zhi-Duan Chen*1 Address: 1State Key Laboratory of Systematic and Evolutionary Botany, Institute of Botany, the Chinese Academy of Sciences, Beijing 100093, China, 2Graduate University of the Chinese Academy of Sciences, Beijing 100039, China, 3Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3DS, UK, 4Department of Ecology & Evolutionary Biology, The University Herbarium, University of Michigan, Ann Arbor, MI 48108-1048, USA, 5Florida Museum of Natural History, University of Florida, Gainesville, FL 32611-7800, USA and 6Arnold Arboretum of Harvard University, 125 Arborway, Jamaica Plain, MA 02130, USA Email: Xin-Yu Zhu - [email protected]; Mark W Chase - [email protected]; Yin-Long Qiu - [email protected]; Hong- Zhi Kong - [email protected]; David L Dilcher - [email protected]; Jian-Hua Li - [email protected]; Zhi- Duan Chen* - [email protected] * Corresponding author Published: 10 November 2007 Received: 19 June 2007 Accepted: 10 November 2007 BMC Evolutionary Biology 2007, 7:217 doi:10.1186/1471-2148-7-217 This article is available from: http://www.biomedcentral.com/1471-2148/7/217 © 2007 Zhu et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. -
Phylogenetic Distribution and Identification of Fin-Winged Fruits
Bot. Rev. (2010) 76:1–82 DOI 10.1007/s12229-010-9041-0 Phylogenetic Distribution and Identification of Fin-winged Fruits Steven R. Manchester1,2 & Elizabeth L. O’Leary1 1 Florida Museum of Natural History, University of Florida, Gainesville, FL 32611-7800, USA 2 Author for Correspondence; e-mail: [email protected] Published online: 9 March 2010 # The New York Botanical Garden 2010 Abstract Fin-winged fruits have two or more wings aligned with the longitudinal axis like the feathers of an arrow, as exemplified by Combretum, Halesia,andPtelea. Such fruits vary in dispersal mode from those in which the fruit itself is the ultimate disseminule, to schizocarps dispersing two or more mericarps, to capsules releasing multiple seeds. At least 45 families and more than 140 genera are known to possess fin-winged fruits. We present an inventory of these taxa and describe their morphological characters as an aid for the identification and phylogenetic assessment of fossil and extant genera. Such fruits are most prevalent among Eudicots, but occur occasionally in Magnoliids (Hernandiaceae: Illigera) and Monocots (Burmannia, Dioscorea, Herreria). Although convergent in general form, fin-winged fruits of different genera can be distinguished by details of the wing number, texture, shape and venation, along with characters of persistent floral parts and dehiscence mode. Families having genera with fin-winged fruits and epigynous perianth include Aizoaceae, Apiaceae, Araliaceae, Asteraceae, Begoniaceae, Burmanniaceae, Combre- taceae, Cucurbitaceae, Dioscoreaceae, Haloragaceae, Lecythidiaceae, Lophopyxida- ceae, Loranthaceae, and Styracaceae. Families with genera having fin-winged fruits and hypogynous perianth include Achariaceae, Brassicaceae, Burseraceae, Celastra- ceae, Cunoniaceae, Cyrillaceae, Fabaceae, Malvaceae, Melianthaceae, Nyctaginaceae, Pedaliaceae, Polygalaceae, Phyllanthaceae, Polygonaceae, Rhamnaceae, Salicaceae sl, Sapindaceae, Simaroubaceae, Trigoniaceae, and Zygophyllaceae. -
Floral Structure and Systematics in Four Orders of Rosids, Including a Broad Survey of floral Mucilage Cells
Pl. Syst. Evol. 260: 199–221 (2006) DOI 10.1007/s00606-006-0443-8 Floral structure and systematics in four orders of rosids, including a broad survey of floral mucilage cells M. L. Matthews and P. K. Endress Institute of Systematic Botany, University of Zurich, Switzerland Received November 11, 2005; accepted February 5, 2006 Published online: July 20, 2006 Ó Springer-Verlag 2006 Abstract. Phylogenetic studies have greatly ened mucilaginous inner cell wall and a distinct, impacted upon the circumscription of taxa within remaining cytoplasm is surveyed in 88 families the rosid clade, resulting in novel relationships at and 321 genera (349 species) of basal angiosperms all systematic levels. In many cases the floral and eudicots. These cells were found to be most structure of these taxa has never been compared, common in rosids, particulary fabids (Malpighi- and in some families, even studies of their floral ales, Oxalidales, Fabales, Rosales, Fagales, Cuc- structure are lacking. Over the past five years we urbitales), but were also found in some malvids have compared floral structure in both new and (Malvales). They are notably absent or rare in novel orders of rosids. Four orders have been asterids (present in campanulids: Aquifoliales, investigated including Celastrales, Oxalidales, Stemonuraceae) and do not appear to occur in Cucurbitales and Crossosomatales, and in this other eudicot clades or in basal angiosperms. paper we attempt to summarize the salient results Within the flower they are primarily found in the from these studies. The clades best supported by abaxial epidermis of sepals. floral structure are: in Celastrales, the enlarged Celastraceae and the sister relationship between Celastraceae and Parnassiaceae; in Oxalidales, the Key words: androecium, Celastrales, Crossoso- sister relationship between Oxalidaceae and Con- matales, Cucurbitales, gynoecium, Oxalidales. -
Stackhousia Stratfordii (Celastraceae: Stackhousioideae), a Remarkable New Species from a Remote Location Near Norseman, South-West Western Australia
W.R.Nuytsia Barker, 21(2): Stackhousia 69–74 (2011) stratfordii (Celastraceae), a new species 69 Stackhousia stratfordii (Celastraceae: Stackhousioideae), a remarkable new species from a remote location near Norseman, south-west Western Australia W.R. (Bill) Barker1 and Geoff T. B. Cockerton2 1State Herbarium of South Australia Hackney Road, Adelaide, South Australia 5000 Australian Centre for Evolutionary Biology and Biodiversity, The University of Adelaide, South Australia 5005 2Western Botanical, PO Box 3393, Bassendean Delivery Centre, Western Australia 6942 Email: [email protected]; [email protected] Abstract Barker W.R. & Cockerton G.T.B. Stackhousia stratfordii (Celastraceae: Stackhousioideae), a remarkable new species from a remote location near Norseman, south-west Western Australia. Nuytsia 21(2): 69–74 (2011). Stackhousia stratfordii W.R.Barker & Cockerton sp. nov. possesses attributes unique to its genus and subfamily of opposite sub-radical leaves and flowers borne in scapes and containing three stamens. Morphological evidence is summarised arguing its placement within Stackhousia. Introduction The Stackhousioideae Burnett are a subfamily distinctive in Celastraceae R.Br. for their herbaceous life-form, mainly moth-pollinated, tubular flowers, and fruits that are single-seeded indehiscent mericarps (cocci) (Barker 1983, 1984, in press); in terms of diversity they are centred in Australia, occurring in much of the continent, in temperate, arid, semi-arid and sub-tropical regions. Until recently a separate family (Stackhousiaceae R.Br.), the subfamily has morphological and geographic features unique in the family Celastraceae, in which they have been placed in the last decade (Kubitzki 2004a, b; Simmons 2004 a, b). It comprises three genera: Tripterococcus Endl. -
Diversity and Evolution of Inflorescences in Celastrales
Feb. 2013, Vol. 7, No. 2, pp. 145-152 Journal of Life Sciences, ISSN 1934-7391, USA Diversity and Evolution of Inflorescences in Celastrales Ivan A. Savinov Department of Microbiology, virology and genetic engineering, Moscow State University of Food Production, Moscow 109316, Russia Received: October 28, 2012 / Accepted: December 21, 2012 / Published: February 28, 2013. Abstract: Inflorescences structures in context of their evolution have been conducted for 60 genera and 170 species of Celastrales (according to APG (Angiosperm Phylogeny Group) III 2009, almost 60% of genera and 15% of species from this taxon of the world flora). There are two big groups of inflorescences in Celastrales-intercalary (more often) and terminal. For many genera of Celastrales both types of inflorescences can be observed, although the frequency of their occurrence varies. There is an important difference between two types of inflorescences: character of completion of the main axis (the terminal flower present or absent). Flower opening can be in basipetal (Celastraceae, Brexia) or acropetal (Stackhousiaceae) order. Partial inflorescence types included: simple, compound or umbrellate dichasia, spike, raceme, thyrse. Simple flowers of Parnassia are large, nested on long reproductive shoots, emerging from a rosette, with amplexicaule leaf. Key words: Celastrales, Celastraceae, Brexia, Parnassia, Stackhousiaceae, inflorescences, structure and development of inflorescences, molecular data. 1. Introduction Following the terminology of Troll [8] and Weberling [9], the inflorescence of Celastrales is In recent times the taxonomic relationship of termed a monotelic synflorescence (rarely polytelic). Celastrales was revised in regards to molecular data As per Kuznetsova [10] and according to the [1-5]. Together with Celastraceae s.str., the genera typological approach of Troll, under inflorescence Parnassia and Brexia and the family Stackhousiaceae (synflorescence) here a system of flowering shoots of were also included in Celastrales. -
Flora.Sa.Gov.Au/Jabg
JOURNAL of the ADELAIDE BOTANIC GARDENS AN OPEN ACCESS JOURNAL FOR AUSTRALIAN SYSTEMATIC BOTANY flora.sa.gov.au/jabg Published by the STATE HERBARIUM OF SOUTH AUSTRALIA on behalf of the BOARD OF THE BOTANIC GARDENS AND STATE HERBARIUM © Board of the Botanic Gardens and State Herbarium, Adelaide, South Australia © Department of Environment, Water and Natural Resources, Government of South Australia All rights reserved State Herbarium of South Australia PO Box 2732 Kent Town SA 5071 Australia J. Adelaide Bot. Gard. 1(2): 69-82 (1977) TAXONOMIC STUDIES IN STACKHOUSIA SM. (STACKHOUSIACEAE) IN SOUTH AUSTRALIA W. R. Barker State Herbarium, Botanic Gardens, North Terrace, Adelaide, South Australia, 5000 Abstract A key to the South Australian species of Stackhousia is presented. S. monogyna Labill., S. aspericocca Schuch. (typified and reinstated as a distinct species although possibly better treated in a future revisionas a race of S. monogyna), S. annua (a new species). S. spathulata Sieb. ex Spreng., and S. megaloptera FvM. (a probablenew record for South Australia) and several other probably undescribed taxa of Sect. Stackhousia Subsect. Cincinniferae Mattf. are recognized as occurring in South Australia. Subsect. Cincinniferae and the polymorphic S. aspericocca require taxonomic study in the context of a revision of the wholegenus. The family Stackhousiaceae is predominantly Australian, with single species in New Zealand and Malesia. The family has been divided by various taxonomists intotwo or three genera, with Stackhousia Sm. the largest and distributed throughout therange of the family. Macgregoria FvM., monotypic and occurring in central Australia,differs markedly from the rest of the family. The monotypic genus Tripterococcus Endl., confined to Western Australia, has flowers similar to Stackhousia and the twogenera are often combined; they differ, however, in gynoecial and fruit characters.