Watsonia Workshop Proceedings of a Workshop Held at the Department of Conservation and Land Management (CALM) on August 4 1993
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Flowering of Watsonia Laccata As Influenced by Corm Storage and Forcing Temperatures ⁎ J.K
Available online at www.sciencedirect.com South African Journal of Botany 77 (2011) 631–637 www.elsevier.com/locate/sajb Flowering of Watsonia laccata as influenced by corm storage and forcing temperatures ⁎ J.K. Suh a, , J.H. Kim a, A.K. Lee a, M.S. Roh b a Dankook University, College of Bio-Resources Science, Department of Environmental Horticulture, Cheonan, Chungnam 330-714, Republic of Korea b US Department of Agriculture, Agricultural Research Service, National Arboretum, Floral and Nursery Plants Research Unit, Beltsville MD 20705, USA Received 24 March 2010; received in revised form 28 November 2010; accepted 22 December 2010 Abstract The genus Watsonia, belonging to the family Iridaceae, is comprised of about 50 species including W. laccata (Jacquin) Ker Gawler that flowers from September to November following low temperature and winter rainfall. Therefore, we hypothesized that flowering would be favored by forcing at low greenhouse temperatures. Using clonal W. laccata corms, four experiments were designed to investigate the effect of temperatures during corm storage, forcing, and their interaction on growth and flowering. Corm formation is favored by growing plants at 18°– 20°/15°–17 °C and 21°–23°/18°–20 °C, day/night temperatures. Flowering was earliest with corms produced at 24°–26°/18°–20 °C and forced at 18°–20/15°–17 °C, and was significantly delayed when forced at 27°–29°/24°–26 °C. Flowering was, however, favored by 2 or 4 weeks of high temperatures (27°–29°/24°–26 °C) prior to forcing at low temperatures (18°–20°/15°–17 °C). The number of florets was not significantly affected by corm storage, forcing temperatures, or their interaction, although forcing at high temperatures tends to reduce the floret number. -
Managing Watsonia Invasion in the Threatened Plant Communities of South-West Australia’S Clay-Based Wetlands
Managing Watsonia invasion in the threatened plant communities of south-west Australia’s clay-based wetlands. K. Brown, G. Paczkowska, B. Huston and N. Withnell. Department of Environment and Conservation, W.A. Email: [email protected] The Seasonal Clay-based Wetlands of South-west Australia While the majority of seasonal wetlands in south-west Australia are connected to the regional ground water, there are a series of wetlands found on clay substrates that rely solely on rainwater to fill. These wetlands are characterised by temporally overlapping suites of annual herbs that flower and set seed as the wetlands dry through spring. Over summer the clay substrates dry to impervious pans. The plant communities of clay-based wetlands comprise a flora of over 600. At least 50% are annual or perennial herbs, 16 occur only on the clay-pans and many are rare or restricted (Figure 1). The seasonally inundated clays that support these communities are relatively productive agricultural soils and many were cleared soon after settlement. Those that remained intact were largely located on the Swan Coastal Plain in close proximity to metropolitan Perth. In more recent years large areas have disappeared under urban development and today the plant communities of seasonal clay-based wetlands are amongst the most threatened in Western Australia. The small and fragmented nature of these remaining wetlands leaves them vulnerable to a range of threatening processes. In particular weed invasion, specifically by the South African geophyte Watsonia (Watsonia meriana var. bulbillifera), is a major threat. Watsonia can disperse via cormels (tiny corms that develop along the flowering stem at the end of the flowering season), into relatively undisturbed bushland remnants, forming dense stands that effectively displace the diverse herbaceous understorey (Figure 2). -
The Effect of Slashing on the Growth of Watsonia Meriana (L.) Mill. Cv Bulbillifera in the Adelaide Hills
Plant Protection Quarterly Vol.8(3) 1993 85 ment of Conservation and Land Manage- ment and Mr. B. Lord of the Charles Sturt University, is gratefully acknowledged. The effect of slashing on the growth of Watsonia meriana (L.) Mill. cv bulbillifera in the Adelaide Hills References Australian Institute of Environmental Studies (1976). ‘The Threat of Weeds to P.A. Wilson and J.G. Conran, Department of Botany, University of Ad- Bushland, a Victorian Study’. (Inkata elaide, SA 5006, Australia. Press, Melbourne, Australia). Gillison, A.N. (1984). Gradient oriented sampling for resource surveys. In ‘Sur- Summary vey Methods for Nature Conservation’, In order to control Watsonia meriana cv suggested that it is merely a local sport ed. K. Myers and D.R. Margules. Vol 2. bulbillifera by slashing, it is necessary to which has been introduced into cultiva- Proceedings of Workshop 1983. prevent flowering and bulbil produc- tion. Currently Watsonia meriana cv Heddle, E.M. (1980). Effects of Changes in tion, as well as reduce the strength of the bulbillifera is considered a weed in Aus- Soil Moisture on the Nature Vegetation corm. The effects of slashing at a tralia, Mauritius, Réunion (Goldblatt of the Northern Swan Coastal Plain, number of heights, and at a range of 1989) and New Zealand (Parsons and Western Australia. Bulletin 92, Forests times throughout the plant’s life-history Cuthbertson 1992). The earliest record in Department of Western Australia. were investigated both for mature South Australia dates from 1842 at Lamont, D. A. (1987). Vegetation Survey plants and those derived from bulbils. Camden Park, Adelaide (Parsons and of Serpentine National Park, Map Plants derived from bulbils require Cuthbertson 1992). -
Wild Watsonia (DPI Vic)
May 2000 Wild watsonia LC0251 Keith Turnbull Research Institute, Frankston ISSN 1329-833X This Landcare Note describes the weed Wild watsonia, West Gippsland, the central highlands and the Geelong Watsonia meriana var. bulbillifera, and related species region. and outlines options for its management. Description Common Name An erect perennial herb forming large clumps; similar to Wild watsonia, bulbil watsonia gladiolus, with strap-like leaves, slender reddish flowering stems 0.5 to 2 m high, pink, orange or red flowers, Botanical Name underground corms and clusters of small corms (known as Watsonia meriana (L.) Miller var. bulbillifera (J.W. bulbils or cormils) on the stems. Leaves and flowering Matthews & L. Bolus) D.A. Cooke heads are produced annually. Family Iridaceae (Iris family) Status Under the Catchment and Land Protection Act, wild watsonia is a Regionally Controlled Weed in the Glenelg, Corangamite, Port Phillip West, Port Phillip East, North East, East Gippsland and West Gippsland Regions. Land owners in areas where wild watsonia is Regionally Controlled must take all reasonable steps to control it and prevent its spread on their land and the roadsides which adjoin their land. Wild watsonia is mainly a weed of roadsides, railway reserves, the edges of water courses, open woodland, unimproved pastures and neglected areas. Origin and Distribution Native to South Africa, wild watsonia was originally introduced to Australia as a garden ornamental. It was considered naturalised in Victoria by 1907 and was spread widely in the 1940s as a fashionable garden plant. It is also a weed in New Zealand and on the Indian Ocean islands of Mauritius and Reunion. -
Bulletin of the UC Santa Cruz Arboretum & Botanic Garden
Bulletin of the UC Santa Cruz Arboretum & Botanic Garden South African Australian New Zealand California Native Aroma/Succulent Butterfly Garden Garden Garden Garden Gardens Garden Contents A day in the gardens this time of year is full of surprises, sometimes Message from the Staff …………………. 1 sunny and hot like a summer day, other times cool and cloudy. No Arboretum News …………………………… 2 matter the weather, the mornings are full of birdsong, fresh air, and calm energy, all Staff & Board Updates ………………….. 2 great for exploring what's blooming—and, if you Watsonia Hybrids ……………………….. 5 find a bench in the gardens and sit still for a few moments, the resident animals will start to Plant Q & A ….......................................... 7 emerge. It’s also a great time to put on your gardening gloves and volunteer to help keep our Gallery of Photos ………………………… 8 gardens gorgeous and thriving. If interested in UCSC Plant Research …………………… 9 joining us, visit the Volunteer webpage to view opportunities available and send in the online Buy Local / Calendar of Events ………… 10 application. —Katie Cordes, Staff & Board Members / Contacts ……. 11 Volunteer Program Coordinator 12 SPRING 2019 BULLETIN 2 Work has already begun on extending the plant sales area behind Norrie’s Gift & Garden Shop, which will enable us to display a much larger quantity of plants year round. The new plant display will add about 800 square feet of area, and plants will all be kept on new nursery tables, rather than on the ground. There will be a railing on the driveway side, partially replacing the large and rotting timber planters now being used to display the plant pots. -
Networks in a Large-Scale Phylogenetic Analysis: Reconstructing Evolutionary History of Asparagales (Lilianae) Based on Four Plastid Genes
Networks in a Large-Scale Phylogenetic Analysis: Reconstructing Evolutionary History of Asparagales (Lilianae) Based on Four Plastid Genes Shichao Chen1., Dong-Kap Kim2., Mark W. Chase3, Joo-Hwan Kim4* 1 College of Life Science and Technology, Tongji University, Shanghai, China, 2 Division of Forest Resource Conservation, Korea National Arboretum, Pocheon, Gyeonggi- do, Korea, 3 Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, United Kingdom, 4 Department of Life Science, Gachon University, Seongnam, Gyeonggi-do, Korea Abstract Phylogenetic analysis aims to produce a bifurcating tree, which disregards conflicting signals and displays only those that are present in a large proportion of the data. However, any character (or tree) conflict in a dataset allows the exploration of support for various evolutionary hypotheses. Although data-display network approaches exist, biologists cannot easily and routinely use them to compute rooted phylogenetic networks on real datasets containing hundreds of taxa. Here, we constructed an original neighbour-net for a large dataset of Asparagales to highlight the aspects of the resulting network that will be important for interpreting phylogeny. The analyses were largely conducted with new data collected for the same loci as in previous studies, but from different species accessions and greater sampling in many cases than in published analyses. The network tree summarised the majority data pattern in the characters of plastid sequences before tree building, which largely confirmed the currently recognised phylogenetic relationships. Most conflicting signals are at the base of each group along the Asparagales backbone, which helps us to establish the expectancy and advance our understanding of some difficult taxa relationships and their phylogeny. -
Phylogeny of Iridaceae Subfamily Crocoideae Based on a Combined Multigene Plastid DNA Analysis Peter Goldblatt Missouri Botanical Garden
Aliso: A Journal of Systematic and Evolutionary Botany Volume 22 | Issue 1 Article 32 2006 Phylogeny of Iridaceae Subfamily Crocoideae Based on a Combined Multigene Plastid DNA Analysis Peter Goldblatt Missouri Botanical Garden T. Jonathan Davies Royal Botanic Gardens, Kew John C. Manning National Botanical Institute Kirstenbosch Michelle van der Bank Rand Afrikaans University Vincent Savolainen Royal Botanic Gardens, Kew Follow this and additional works at: http://scholarship.claremont.edu/aliso Part of the Botany Commons Recommended Citation Goldblatt, Peter; Davies, T. Jonathan; Manning, John C.; van der Bank, Michelle; and Savolainen, Vincent (2006) "Phylogeny of Iridaceae Subfamily Crocoideae Based on a Combined Multigene Plastid DNA Analysis," Aliso: A Journal of Systematic and Evolutionary Botany: Vol. 22: Iss. 1, Article 32. Available at: http://scholarship.claremont.edu/aliso/vol22/iss1/32 MONOCOTS Comparative Biology and Evolution Excluding Poales Aliso 22, pp. 399-41 I © 2006, Rancho Santa Ana Botanic Garden PHYLOGENY OF IRIDACEAE SUBFAMILY CROCOIDEAE BASED ON A COMBINED MULTIGENE PLASTID DNA ANALYSIS 1 5 2 PETER GOLDBLATT, · T. JONATHAN DAVIES, JOHN C. MANNING,:l MICHELLE VANDER BANK,4 AND VINCENT SAVOLAINEN2 'B. A. Krukoff Curator of African Botany, Missouri Botanical Garden, St. Louis, Missouri 63166, USA; 2Molecular Systematics Section, Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3DS, UK; 3National Botanical Institute, Kirstenbosch, Private Bag X7, Cape Town, South Africa; 4 Botany Department, Rand Afrikaans University, Johannesburg, South Africa 5 Corresponding author ([email protected]) ABSTRACT The phylogeny of Crocoideae, the largest of four subfamilies currently recognized in Tridaceae, has eluded resolution until sequences of two more plastid DNA regions were added here to a previously published matrix containing sequences from four DNA plastid regions. -
Wild Watsonia Common and Scientific Names
Source: http://agriculture.vic.gov.au/agriculture/pests-diseases-and-weeds/weeds/a-z-of- weeds/wild-watsonia Downloaded 15/12/2015. Wild Watsonia Common and scientific names Wild watsonia, bulbil watsonia Watsonia meriana (L.) Miller var. bulbillifera (J.W. Matthews & L. Bolus) D.A. Cooke Family Iridaceae (Iris family) Origin and distribution Native to South Africa, wild watsonia was originally introduced to Australia as a garden ornamental. It was considered naturalised in Victoria by 1907 and was spread widely in the 1940s as a fashionable garden plant. It is also a weed in New Zealand and on the Indian Ocean islands of Mauritius and Reunion. It has a number of undesirable horticultural features and may best be classified as a variety that evolved naturally in an environment subject to human disturbance rather than a cultivar. Fertile plants producing seed are rare in Australia and some authors consider bulbil watsonia to be sterile. Wild watsonia is found through most of the State except for the north-west, but mainly occurs as an environmental weed in depressions and swampy areas on heavier soils in southern Victoria, particularly in the Melbourne area, Dandenong Ranges, Mornington Peninsula, South and West Gippsland, the central highlands and the Geelong region. Description An erect perennial herb forming large clumps; similar to gladiolus, with strap-like leaves, slender reddish flowering stems 0.5 to 2 m high, pink, orange or red flowers, underground corms and clusters of small corms (known as bulbils or cormils) on the stems. Leaves and flowering heads are produced annually. Corms and cormils start to grow in late autumn and foliage is produced during the winter. -
Prospects for Biological Control of Watsonia Species Species (Table 1)
90 Plant Protection Quarterly Vol.8(3) 1993 Kloot, P.M. (1987c). The naturalized flora of South Australia. 3. Its origin, intro- duction, distribution, growth forms and significance. Journal of the Adelaide Botanic Gardens 10, 99-111. Menz, K.M. and Auld, B.A. (1977). Gal- vanized burr control and public policy toward weeds. Search 8, 281-7. Pate, J.S. and Dixon, K.W. (1982). ‘Tuber- ous, cormous and bulbous plants’. (University of Western Australia Press, Nedlands). Parsons, W.T. and Cuthbertson, E.G. (1992). ‘Noxious weeds of Australia’. (Inkata Press, Melbourne, Australia). Phillips, R. and Rix, M. (1989). ‘Bulbs’. 2nd edition. (Pan Books, London, UK). Wilkinson, L. (1990). Systat, the system for statistics, version 5.0. Systat Inc., Champaign, Illinois, USA. Zar, J.H. (1986). ‘Biostatistical analysis’. 2nd edition. (Prentice-Hall, New Jer- sey, USA). Figure 6. The response of corm production to slashing at selected intervals. The time interval between 1, 2 and 3 is two weeks; the remaining intervals one week. Labels indicate those points which are significantly different: Gumeracha (g), Balhannah (b), both of the other sites (*). erences to organisms attacking Watsonia Prospects for biological control of Watsonia species species (Table 1). Most records are of polyphagous or pest organisms and need not be considered further. Le Maitre John K. Scott, CSIRO Division of Entomology, Private Bag, PO Wembley, (1984) observed that up to 78.1% of ova- WA 6014, Australia. ries had been bored or partly eaten by in- sects in a study of seed predation of Summary concern with the invasion of Watsonia Watsonia borbonica (Pourret) Goldblatt in Watsonia species are suitable targets for species into native vegetation has lead to South Africa. -
Plant Nomenclature - Flowers Common Name: Botanical Latin Name: Family Name Amaryllis Hippeastrum (Amaryllidaceae) Apple; Flowering Apple, Crab Apple Malus Spp
Plant Nomenclature - Flowers Common Name: Botanical Latin Name: Family Name Amaryllis Hippeastrum (Amaryllidaceae) Apple; Flowering Apple, Crab Apple Malus spp. (Rosaceae) Autumn Joy Sedum Sedum ‘Autumn Joy’ (Crassulaceae) Baby’s Breath Gypsophila paniculata (Caryophyllaceae) Bachelor's buttons, Cornflower Centaurea cyannus (Asteraceae – Compositae) Balloon Flower Platycodon grandiflorus (Campanulaceae – Lobeliaceae) Banana Shrub Michelia fuscata; M. figo (Magnoliaceae) Banksia Banksia spp. (Proteaceae) Begonia Begonia (Begoniaceae) Bellflower Campanula spp. (Campanulaceae – Lobeliaceae) Bells of Ireland Moluccella laevis (Lamiaceae- Labiatae) Billy Balls or Billy Buttons Craspedia globosa (Asteraceae - Compositae) Bird of Paradise Strelitzia reginae (Streliziaceae) Black-Eyed Susan Rudbekia spp. (Asteraceae- Compositae) Blanket Flower Gaillardia spp. (Asteraceae – Compositae) Blue Mist Flower, Hardy ageratum Eupatorium coelestinum syn. (Asteraceae – Compositae) Conoclinium coelestinum Blue Throatwort Trachelium caeruleum (Campanulaceae – Lobeliaceae) Bouvardia Bouvardia spp. (Rubiaceae) Breath of Heaven Coleonema pulchrum(Diosma) (Rutaceae) Brodiaea; also Triteleia Brodiaea spp . (Liliaceae) Broom Genista spp. (Fabaceae – Leguminosae) Buttercup; Ranunculus Ranunuclus spp. (Ranunculaceae) Butterfly Bush Buddleia davidii (Buddlejaceae) Butterfly Weed Asclepias tuberose (Asclepiadaceae) Calla Lily Zantedeschia spp. (Araceae) Camellia Camellia spp. (Theaceae) Candytuft Iberis spp. (Brassicaceae – Cruciferae) Chinese Lantern Lily Sandersonia -
Genetics of White-Flowered Cultivars Derived from Watsonia Borbonica (Iridaceae) D.A
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 © 2010 Board of the Botanic Gardens & State Herbarium, Government of South Australia J. Adelaide Bot. Gard. 24 (2010) 33–38 © 2010 Department of Environment and Natural Resources, Government of South Australia Genetics of white-flowered cultivars derived from Watsonia borbonica (Iridaceae) D.A. Cooke 58 Gardiner Avenue, Warradale, South Australia 5046 Email: [email protected] Abstract Breeding experiments suggest that the occurrence of white (acyanic) flowers in several cultivars derived from Watsonia borbonica (Pourr.) Goldblatt is determined by a single recessive allele. Many Watsonia cultivars have been characterised simply as ‘white-flowered’; but descriptions based on several characters are necessary if cultivars with unique genotypes are to be differentiated without ambiguity. Keywords: Watsonia, Iridaceae, cultivated plants Introduction Plants with anthocyanin-pigmented flowers normally The chemical pathways by which flavonoids, produce at least traces of red-purple pigmentation in including the red to blue coloured anthocyanins, are the leaves and stems, particularly under conditions of synthesised in plants have been thoroughly documented stress. However, acyanic variants typically have pure (Winkel-Shirley 2001). As these pathways are similar green leaves and stems as these also lack anthocyanins. -
Flora of Australia, Volume 46, Iridaceae to Dioscoreaceae
FLORA OF AUSTRALIA Volume 46 Iridaceae to Dioscoreaceae This volume was published before the Commonwealth Government moved to Creative Commons Licensing. © Commonwealth of Australia 1986. 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, no part may be reproduced or distributed by any process or stored in any retrieval system or data base without prior written permission from the copyright holder. Requests and inquiries concerning reproduction and rights should be addressed to: [email protected] FLORA OF AUSTRALIA The nine families in this volume of the Flora of Australia are Iridaceae, Aloeaceae, Agavaceae, Xanthorrhoeaceae, Hanguan- aceae, Taccaceae, Stemonaceae, Smilacaceae and Dioscoreaceae. The Xanthorrhoeaceae has the largest representation with 10 genera and 99 species. Most are endemic with a few species of Lomandra and Romnalda extending to neighbouring islands. The family includes the spectacular blackboys and grass-trees. The Iridaceae is largely represented by naturalised species with 52 of the 78 species being introduced. Many of the introductions are ornamentals and several have become serious weeds. Patersonia is the largest genus with all 17 species endemic. Some of these are cultivated as ornamentals. The Dioscoreaccae is a family of economic significance, particularly in the old world tropics where some species are cultivated or collected for their tubers and bulbils. In Australia there are 5 species, one of which is a recent introduction. The endemic and native species, commonly known as yams, are traditionally eaten by the Aborigines.