Rhamnaceae Study Group
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Seed Ecology Iii
SEED ECOLOGY III The Third International Society for Seed Science Meeting on Seeds and the Environment “Seeds and Change” Conference Proceedings June 20 to June 24, 2010 Salt Lake City, Utah, USA Editors: R. Pendleton, S. Meyer, B. Schultz Proceedings of the Seed Ecology III Conference Preface Extended abstracts included in this proceedings will be made available online. Enquiries and requests for hardcopies of this volume should be sent to: Dr. Rosemary Pendleton USFS Rocky Mountain Research Station Albuquerque Forestry Sciences Laboratory 333 Broadway SE Suite 115 Albuquerque, New Mexico, USA 87102-3497 The extended abstracts in this proceedings were edited for clarity. Seed Ecology III logo designed by Bitsy Schultz. i June 2010, Salt Lake City, Utah Proceedings of the Seed Ecology III Conference Table of Contents Germination Ecology of Dry Sandy Grassland Species along a pH-Gradient Simulated by Different Aluminium Concentrations.....................................................................................................................1 M Abedi, M Bartelheimer, Ralph Krall and Peter Poschlod Induction and Release of Secondary Dormancy under Field Conditions in Bromus tectorum.......................2 PS Allen, SE Meyer, and K Foote Seedling Production for Purposes of Biodiversity Restoration in the Brazilian Cerrado Region Can Be Greatly Enhanced by Seed Pretreatments Derived from Seed Technology......................................................4 S Anese, GCM Soares, ACB Matos, DAB Pinto, EAA da Silva, and HWM Hilhorst -
Rhamnaceae) Using Scanning Electron Microscopy Jürgen Kellermanna,B
Swainsona 33: 75–102 (2020) © 2020 Board of the Botanic Gardens & State Herbarium (Adelaide, South Australia) A preliminary survey of the leaf-indumentum in the Australian Pomaderreae (Rhamnaceae) using Scanning Electron Microscopy Jürgen Kellermanna,b a State Herbarium of South Australia, GPO Box 1047, Adelaide, South Australia 5001 Email: [email protected] b School of Biological Sciences, Adelaide, The University of Adelaide, South Australia 5005 Abstract: The tribe Pomaderreae (10 genera, c. 240 species) is almost endemic to Australia and defined within Rhamnaceae by the presence of ‘stellate hairs’. This paper is the first to report observations on the leaf-indumentum of 33 species of the tribe with Scanning Electron Microscopy. Apart from simple hairs and papillae, three types of stellate trichomes were observed: fasciculate hairs, appressed stellate hairs and multiradiate hairs (sessile or stalked). The existence of stellate trichomes on the examined species of Pomaderreae was confirmed. Trichomes and indumenta are often variable within genera, as the type of indumentum may be more related to its function. Some groups of species in the genera Cryptandra Sm., Pomaderris Labill. and Stenanthemum Reissek have indumentum characters that seem to be more consistent and might be of value to elucidate relationships between taxa. Keywords: Rhamnaceae, Pomaderreae, leaf morphology, trichomes, hairs, leaf surface, SEM Introduction xeromorphic adaptations, such as small, hard, revolute or conduplicate leaves, a dense indumentum or spines. Pomaderreae Reissek ex Endl. is the second largest tribe of Rhamnaceae. It was first described by Reissek On-going molecular and morphological studies in (1840), but not accepted by subsequent botanists (e.g. -
Pomaderris Amoena
Pomaderris amoena COMMON NAME Tauhinu SYNONYMS Pomaderris phylicifolia var. ericifolia (Hook.) L.B.Moore, P. ericifolia Hook. FAMILY Rhamnaceae AUTHORITY Pomaderris amoena Colenso FLORA CATEGORY Vascular – Native ENDEMIC TAXON Yes ENDEMIC GENUS Pomaderris amoena close up of flowers and No foliage. Photographer: John Smith-Dodsworth ENDEMIC FAMILY No STRUCTURAL CLASS Trees & Shrubs - Dicotyledons NVS CODE POMAMO CHROMOSOME NUMBER 2n = 36 Pomaderris amoena plant. Photographer: John Smith-Dodsworth CURRENT CONSERVATION STATUS 2012 | Not Threatened PREVIOUS CONSERVATION STATUSES 2009 | Not Threatened 2004 | Not Threatened BRIEF DESCRIPTION Locally very common small shrub to 1m tall with hairy twigs bearing masses of small narrow wrinkled leaves and clusters of white flowers. Leaves 5-10mm long by 1-2mm wide, margins inrolled to almost cover the underside. Fruit dry, small. DISTRIBUTION Endemic. Three Kings, North and South Islands. In the South Island generally scarce reaching its southern limit at Eyrewell Forest, Canterbury; south of Auckland it is mainly east of main ranges in North Island. HABITAT Usually coastal and lowland open shrublands, gumland scrub and in sand country. Also in rocky headlands, gravel river terraces. Occasionally found well inland in montane situations. A species virtually confined to successional vegetation types FLOWER COLOURS White, Yellow PROPAGATION TECHNIQUE Difficult. Can be grown from semi-hardwood cuttings and seed but seed is hard to germinate. The best results seem to be from cuttings rooted in untreated sawdust. Once plants are established they grow very well and make an attractive flowering shrub for an open, sunny post. It does best in nutrient-poor, well-drained soil ETYMOLOGY pomaderris: Lid skin amoena: Beautiful, pleasing TAXONOMIC NOTES The New Zealand plant has been treated as P. -
VINEYARD BIODIVERSITY and INSECT INTERACTIONS! ! - Establishing and Monitoring Insectariums! !
! VINEYARD BIODIVERSITY AND INSECT INTERACTIONS! ! - Establishing and monitoring insectariums! ! Prepared for : GWRDC Regional - SA Central (Adelaide Hills, Currency Creek, Kangaroo Island, Langhorne Creek, McLaren Vale and Southern Fleurieu Wine Regions) By : Mary Retallack Date : August 2011 ! ! ! !"#$%&'(&)'*!%*!+& ,- .*!/'01)!.'*&----------------------------------------------------------------------------------------------------------------&2 3-! "&(')1+&'*&4.*%5"/0&#.'0.4%/+.!5&-----------------------------------------------------------------------------&6! ! &ABA <%5%+3!C0-72D0E2!AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA!F! &A&A! ;D,!*2!G*0.*1%-2*3,!*HE0-3#+3I!AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA!J! &AKA! ;#,2!0L!%+D#+5*+$!G*0.*1%-2*3,!*+!3D%!1*+%,#-.!AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA!B&! 7- .*+%)!"/.18+&--------------------------------------------------------------------------------------------------------------&,2! ! ! KABA ;D#3!#-%!*+2%53#-*MH2I!AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA!BN! KA&A! O3D%-!C#,2!0L!L0-H*+$!#!2M*3#G8%!D#G*3#3!L0-!G%+%L*5*#82!AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA!&P! KAKA! ?%8%53*+$!3D%!-*$D3!2E%5*%2!30!E8#+3!AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA!&B! 9- :$"*!.*;&5'1/&.*+%)!"/.18&-------------------------------------------------------------------------------------&3<! -
A Phylogenetic Analysis of Rhamnaceae Using Rbcl and Trnl-F Plastid DNA Sequences James E. Richardson
A Phylogenetic Analysis of Rhamnaceae using rbcL and trnL-F Plastid DNA Sequences James E. Richardson; Michael F. Fay; Quentin C. B. Cronk; Diane Bowman; Mark W. Chase American Journal of Botany, Vol. 87, No. 9. (Sep., 2000), pp. 1309-1324. Stable URL: http://links.jstor.org/sici?sici=0002-9122%28200009%2987%3A9%3C1309%3AAPAORU%3E2.0.CO%3B2-5 American Journal of Botany is currently published by Botanical Society of America. Your use of the JSTOR archive indicates your acceptance of JSTOR's Terms and Conditions of Use, available at http://www.jstor.org/about/terms.html. JSTOR's Terms and Conditions of Use provides, in part, that unless you have obtained prior permission, you may not download an entire issue of a journal or multiple copies of articles, and you may use content in the JSTOR archive only for your personal, non-commercial use. Please contact the publisher regarding any further use of this work. Publisher contact information may be obtained at http://www.jstor.org/journals/botsam.html. Each copy of any part of a JSTOR transmission must contain the same copyright notice that appears on the screen or printed page of such transmission. The JSTOR Archive is a trusted digital repository providing for long-term preservation and access to leading academic journals and scholarly literature from around the world. The Archive is supported by libraries, scholarly societies, publishers, and foundations. It is an initiative of JSTOR, a not-for-profit organization with a mission to help the scholarly community take advantage of advances in technology. -
Notes on Stenanthemum Reissek (Rhamnaceae: Pomaderreae) and a Key to the Genus in Australia Jürgen Kellermanna,B & Kevin R
Swainsona 35: 11–22 (2021) © 2021 Board of the Botanic Gardens & State Herbarium (Adelaide, South Australia) The other ‘propeller plant’ – Notes on Stenanthemum Reissek (Rhamnaceae: Pomaderreae) and a key to the genus in Australia Jürgen Kellermanna,b & Kevin R. Thielec a State Herbarium of South Australia, Botanic Gardens and State Herbarium, Hackney Road, Adelaide, South Australia 5000 Email: [email protected] b The University of Adelaide, School of Biological Sciences, Adelaide, South Australia 5005 c School of Biological Sciences, University of Western Australia, 35 Stirling Hwy, Crawley (Perth), Western Australia 6009 Email: [email protected] Abstract: Descriptions are provided for ten taxa of Stenanthemum Reissek published in the 19th century and their typification is clarified. Lectotypes are chosen for St. divaricatum (Benth.) Rye, St. humile Benth., St. leucophractum (Schltdl.) Reissek, St. pimeleoides (Hook.f.) Benth., St. pumilum (F.Muell.) Diels and Cryptandra subgen. Solenandra Reissek (a synonym of Stenanthemum). A key to all species and subspecies of the genus, which is endemic in Australia, is provided. Keywords: Nomenclature, typification, identification key, Rhamnaceae, Pomaderreae, Stenanthemum, Australia Introduction The concept of Hooker (1862) and Bentham (1863) was generally followed by subsequent authors, but Stenanthemum Reissek contains c. 30 species, most Mueller (1875) still included the genus in Spyridium endemic to Western Australia (Rye 1995, 2001, 2007), when describing Sp. pumilum F.Muell., a species that but eight species occur in other States, as outlined in Diels & Pritzl (1904) transferred to Stenanthemum as Thiele (2007). The taxonomic history of the genus was St. pumilum (F.Muell) Diels. discussed in Kellermann (2007) and Thiele (2007). -
Fire Retardant Plants for the Urban Fringe and Rural Areas
Flammability Groups Leptospermum scoparium TN Pittosporum undulatum AN X Cucurbita maxima E Pumpkin Morus sp. E Mulberry Manuka, Teatree Sweet Pittosporum Cymbopogon citratus E Lemon Grass Myoporum insulare AN Boobyalla In the following list E denotes an exotic plant, TN a plant Lomandra longifolia TN Saggs Platanus x acerifolia E Plane Tree Cyphomandra betacea E Tamarillo Nerium oleander E Oleander native to Tasmania, AN a plant native to mainland Australia Melaleuca alternifolia AN Paperbark Poa sp. AN Poa Grass Delonix regia E Poinciana Olearia argophylla TN Musk Monstera deliciosa E Monstera Populas sp. E Poplar and X a known environmental weed. Dicksonia antarctica TN Man Fern Photinia glabra var. rubens E Nadina domestica E Sacred Bamboo Quercus robur E English oak Diospryros sp. E Persimmon Chinese Fire Bush or Red-leafed Photinia High Flammability Nicotiana glauca AN Tobacco Bush Spiraea catoniensis E May Eriobotrya japonica E Loquat Pittosporum bicolor TN Cheesewood Pinus elliottii E Tasmannia lanceolata TN Escallonia macrantha E Escallonia These plants have been shown to be highly flammable and Slash or Elliott’s Pine Native Pepper Pteridium esculentum TN Euryops pectinatus E Bracken Fern should not be planted or allowed to remain inside your house’s Pinus patula E Ulex europaeus E X Gorse Yellow Daisy Bush Mexican or Weeping Pine Rhododendron sp. E Rhododendron Building Protection Zone. They should also be avoided in the Viburnum opulus E Guelder Rose Genista monspessulana E X Montpellier Broom Rosa sp. E X Roses, Briars Fuel Modified Zone. Move these plants away from your house Moderate Flammability Koelreuteria paniculata E Salix babylonica E Weeping Willow and replace them with less flammable plants. -
Tribe Species Secretory Structure Compounds Organ References Incerteae Sedis Alphitonia Sp. Epidermis, Idioblasts, Cavities
Table S1. List of secretory structures found in Rhamanaceae (excluding the nectaries), showing the compounds and organ of occurrence. Data extracted from the literature and from the present study (species in bold). * The mucilaginous ducts, when present in the leaves, always occur in the collenchyma of the veins, except in Maesopsis, where they also occur in the phloem. Tribe Species Secretory structure Compounds Organ References Epidermis, idioblasts, Alphitonia sp. Mucilage Leaf (blade, petiole) 12, 13 cavities, ducts Epidermis, ducts, Alphitonia excelsa Mucilage, terpenes Flower, leaf (blade) 10, 24 osmophores Glandular leaf-teeth, Flower, leaf (blade, Ceanothus sp. Epidermis, hypodermis, Mucilage, tannins 12, 13, 46, 73 petiole) idioblasts, colleters Ceanothus americanus Idioblasts Mucilage Leaf (blade, petiole), stem 74 Ceanothus buxifolius Epidermis, idioblasts Mucilage, tannins Leaf (blade) 10 Ceanothus caeruleus Idioblasts Tannins Leaf (blade) 10 Incerteae sedis Ceanothus cordulatus Epidermis, idioblasts Mucilage, tannins Leaf (blade) 10 Ceanothus crassifolius Epidermis; hypodermis Mucilage, tannins Leaf (blade) 10, 12 Ceanothus cuneatus Epidermis Mucilage Leaf (blade) 10 Glandular leaf-teeth Ceanothus dentatus Lipids, flavonoids Leaf (blade) (trichomes) 60 Glandular leaf-teeth Ceanothus foliosus Lipids, flavonoids Leaf (blade) (trichomes) 60 Glandular leaf-teeth Ceanothus hearstiorum Lipids, flavonoids Leaf (blade) (trichomes) 60 Ceanothus herbaceus Idioblasts Mucilage Leaf (blade, petiole), stem 74 Glandular leaf-teeth Ceanothus -
Three Species of Cryptandra (Rhamnaceae: Pomaderreae) from Southern Australia Allied to C
Swainsona 33: 125–134 (2020) © 2020 Board of the Botanic Gardens & State Herbarium (Adelaide, South Australia) Three species of Cryptandra (Rhamnaceae: Pomaderreae) from southern Australia allied to C. tomentosa Jürgen Kellermanna,b a State Herbarium of South Australia, Botanic Gardens and State Herbarium, Hackney Road, Adelaide, South Australia 5001 Email: [email protected] b The University of Adelaide, School of Biological Sciences, Adelaide, South Australia 5005 Abstract: Two species of Cryptandra are described as new, C. setifera Kellermann and C. sabulicola Kellermann, and C. campanulata Schltdl. is formally reinstated. The species are described and illustrated, synonymies are provided, as well as an identification key for the C. amara-tomentosa complex in Victoria and South Australia. Specimens of all three taxa have formerly been identified as C. amara Sm. or C. tomentosa Lindl., but are clearly separate from them. Keywords: New species, Rhamnaceae, Cryptandra, South Australia, Victoria Introduction Kellermann, is native to deep sands in northern Eyre Peninsula and on both sides of the South Australian- Cryptandra Sm. is a genus of about 60 species, mainly Victorian border, especially in and around Billiat distributed in southern Western Australia and south- Conservation Park (C.P.), Murray-Sunset National Park eastern Australia, with a few species occurring in the (N.P.) and the Big Desert. Cryptandra campanulata north of the continent. During the last 25 years, research Schltdl. grows in rocky habitats of the northern Mount on the genus was undertaken in Western Australia Lofty Ranges and southern Flinders Ranges. (Rye 1995, 2007; Rye & Trudgen 1995), Queensland (Bean 2004) and Victoria (Walsh & Udovicic 1999). -
Research Indicators – Herbarium
State Herbarium of South Australia Research Prospectus 2008–09 The State’s key institution for advancing and disseminating knowledge of plants, algae and fungi Table of Contents Overview..............................................................................................................................3 Background .........................................................................................................................3 Reporting .........................................................................................................................3 History..............................................................................................................................3 Vision & Mission ..................................................................................................................5 Research expertise, strengths and opportunities.................................................................6 Background......................................................................................................................6 Current strengths .............................................................................................................7 Taxonomic expertise ........................................................................................................8 Key groups.......................................................................................................................9 Opportunities .....................................................................................................................10 -
Pomaderris Sericea
Plants of South Eastern New South Wales Line drawings. b. leaf outline; leaf lower surface detail; flower. A. Barley, National Herbarium of Victoria, © 2021 Royal Botanic Gardens Board Common name Silky pomaderris, Bent pomaderris Family Rhamnaceae Where found Open forest, shrubland, rocky areas, and along streams. Morton National Park and Wollemi National Park. Notes Shrub to about 2 m high. Branchlets shining golden-brown with short appressed simple hairs. Leaves alternating up the stems, 0.6–3 cm long, 2–10 mm wide, upper surface hairless; lower surface with appressed shining golden-brown simple hairs, entirely obscuring the underlying stellate hairs (needs a hand lens or a macro app on your phone/tablet to see), lateral veins obscure, tips blunt, margins curved down. Flowers cream to yellow, with 5 sepals each 1.7–2.1 mm long, falling early, and 0 petals, in branched clusters 10–30 mm long and wide. Flowers Oct. Vulnerable Australia. Endangered NSW. Provisions of the NSW Biodiversity Conservation Act 2016 No 63 relating to the protection of protected plants generally also apply to plants that are a threatened species. Vulnerable Vic. Listed in the Flora and Fauna Guarantee Act, Vic. NSW Threatened Species profile: http://www.environment.nsw.gov.au/threatenedspeciesapp/profile.aspx?id=10658 (accessed 7 January 2021) PlantNET description: http://plantnet.rbgsyd.nsw.gov.au/cgi-bin/NSWfl.pl?page=nswfl&lvl=sp&name=Pomaderris~sericea (accessed 7 January 2021) Author: Betty Wood. This identification key and fact sheets are available as a free mobile application: Android edition iOS edition Creative Commons Attribution 3.0 Australia (CC BY). -
Robert Brown's Contributions to Rhamnaceae Systematics
515 Robert Brown‘s contributions to Rhamnaceae systematics Jürgen Kellermann Abstract Kellermann, Jürgen (School of Botany, The University of Melbourne, Vic 3010, Australia. Email: [email protected]) 2004. Robert Brown ‘s contributions to Rhamnaceae systematics. Telopea 10(2): 515–524. This paper outlines the taxonomic history of Rhamnaceae Juss. during the first half of the 19th century, with a focus on Robert Brown’s contributions. Brown advanced Rhamnaceae systematics in two ways. Firstly, he collected 31 species of the family during his time in Australia (1801–1805); nearly all of them were new to science. Although he did not publish any taxa from these collections himself, they were instrumental for his second contribution. In 1814, Robert Brown gave the family a definition that is still valid today. Brown split Rhamnaceae sensu Juss. into Celastraceae R.Br. and Rhamnaceae s.str. (i.e. sensu R.Br.). Some remaining genera had to be dispersed into a number of other families, such as Aquifoliaceae, Oleaceae or Staphyleaceae. Introduction The Rhamnaceae Juss. is a medium sized plant family, with 900–1000 species worldwide. The taxon was established by Michel Adanson in the Familles des plantes as ‘Ziziphi’ (Adanson 1763), followed by Antoine-Laurent de Jussieu, who treated it as ‘Rhamni’ in his Genera plantarum (Jussieu 1789). Both authors included a variety of genera in their treatments, many of which are now attributed to other families, for example Celastraceae R.Br., Oleaceae Hoffsgg. & Link or Staphyleaceae Martinov (see Table 2 for a detailed analysis of Jussieu’s genera). Jussieu seems also to have had doubts about the uniformity of his ‘Rhamni’ (Harms 1953), since he asks himself: “An indè dividendus ordo?” (Jussieu 1789: 383).