Swainsona Murrayana

Total Page:16

File Type:pdf, Size:1020Kb

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.). Grows in a variety of vegetation types including bladder saltbush, black box and grassland communities. The species may require some disturbance, plants have been found in remnant native grasslands or grassy woodlands that have been intermittently grazed or cultivated. Plants produce winter-spring growth, flower in spring to early summer and then die back after flowering. They re-shoot readily and often carpet the landscape after good cool-season rains. Swainsona species contain a poisoning principle, swainsonine, which affects the nervous system and is toxic to stock (Department of Environment and Conservation 2005). System Movement pattern Crop Wild Relative Terrestrial Freshwater Nomadic Congregatory/Dispersive Is the species a wild relative of a crop? Marine Migratory Altitudinally migrant Life History Age at Maturity Female: Units for Age: Male: Size at Maturity (in cm) Female: Male: Longevity: Units for Longevity: Averate Reproductive Age: Units for Reproductive Age: Maximum Size (in cm): Size at Birth (in cm): Gestation Time: Units for Gestation: Generation Length: Justification: Reproductive Periodicity: Average Annual Fecundity or Litter Size: Annual Rate of Population Increase: Annual Rate of Population Increase: Natural Mortality: Growth From Definition Forb or Herb Biennial or perennial herbacaeous plant, also termed a Hemicryptophyte Threats The main identified threats to Slender Darling-pea include: grazing from domestic stock and rabbits especially in the flowering season when grazing could influence the soil seed bank and hence future abundance of the species; loss of habitat to cultivation particularly rice crops, weed invasion, increased salination, frequency of fires and urban development (Department of Environment and Conservation 2005). This species should not be burnt more frequently than once every ten years (NSW RFS 2004; Threatened Species Scientific Committee 2008). Past Present Future 1 Habitat Loss/Degradation (human induced) 1.1 Agriculture 1.1.1 Crops 1.1.4 Livestock 1.4 Infrastructure development 1.4.2 Human settlement 1.5 Invasive alien species (directly impacting habitat) 1.7 Fires 2 Invasive alien species (directly affecting the species) 2.2 Predators 7 Natural disasters 7.4 Wildfire 8 Changes in native species dynamics 8.1 Competitors 8.3 Prey/food base 10 Human disturbance 10.5 Fire Conservation Measures It is known to occur within several protected areas, most notably in Victoria it occurs in the James Barret Flora and Fauna Reserve and the Terrick Terrick National Park (with ~42,000 known individuals) (DSE 2003). This species is eligible for listing as Vulnerable under the Environment Protection and Biodiversity Conservation Act 1999 (EPBC Act). Also listed as 3VCi (Briggs and Leigh 1996), a vulnerable species with a geographic range more than 100 km2 with less than 1,000 plants known to occur within a protected area. Slender Darling-pea is also listed as threatened under the Flora and Fauna Guarantee Act 1998 (Victoria) and Vulnerable under the Threatened Species Conservation Act 1995 (NSW), the Nature Conservation Act 1992 (Queensland), 1997 IUCN red list of threatened plants and the National Parks and Wildlife Act 1972 (South Australia). The seeds for this species have been collected as part of the Millennium Seed Bank project. Seeds are located at: Wakehurst Place, Royal Botanic Gardens, Kew (UK) and the Seed Conservation Centre, Adelaide Botanic Garden, South Australia (Australia). The distribution of this species overlaps with several EPBC Act-listed threatened ecological communities. Management actions to protect this species include: control of herbivorous pests and grazing pressure, protection of the species from further urban/agricultural development, further research on its ecology, population size and impacts from threats (Threatened Species Scientific Committee 2008; Department of Environment and Conservation 2005). In Place Needed 1 Policy-based actions 1.1 Management plans 1.1.1 Development 1.1.2 Implementation 1.2 Legislation 1.2.1 Development 1.2.1.2 National level 1.2.1.3 Sub-national level 3 Research actions 3.3 Biology and Ecology 3.4 Habitat status 3.5 Threats 4 Habitat and site-based actions 4.4 Protected areas 5 Species-based actions 5.7 Ex situ conservation actions 5.7.2 Genome resource bank Countries of Occurrence PRESENCE ORIGIN Year Breeding Non- Passage Possibly ExtinctPresence Native Introduced Re- Vagrant Origin Round Season breeding migrant extinct uncertain Introduced uncertain only season only Australia New South Wales Queensland South Australia Victoria General Habitats Score Description Major Importance 2 Savanna 1UnsetSuitable 2.1 Savanna - Dry1Unset Suitable 3 Shrubland 1UnsetSuitable 3.4 Shrubland - Temperate1Unset Suitable 4 Grassland 1UnsetSuitable 4.4 Grassland - Temperate1Unset Suitable 5 Wetlands (inland)1Unset Suitable 5.3 Wetlands (inland) - Shrub Dominated Wetlands1Unset Suitable 5.4 Wetlands (inland) - Bogs, Marshes, Swamps, Fens, Peatlands1Unset Suitable 14 Artificial/Terrestrial1Unset Suitable 15 Artificial/Aquatic & Marine1Unset Suitable 15.7 Artificial/Aquatic - Irrigated Land (includes irrigation channels)1Unset Suitable 15.8 Artificial/Aquatic - Seasonally Flooded Agricultural Land1Unset Suitable Species Utilisation Species is not utilised at all Trend in the level of wild offtake/harvest in relation to total wild population numbers over the last five years: Trend in the amount of offtake/harvest produced through domestication/cultivation over the last five years: CITES status: Not listed IUCN Red Listing Red List Assessment:(using 2001 IUCN system) Vulnerable (VU) Red List Criteria: A3c Date Last Seen (only for EX, EW or Possibly EX species): Is the species Possibly Extinct? Possibly Extinct Candidate? Rationale for the Red List Assessment S. murrayana is a herb that is scattered in grassy ecosystems in seasonally inundated sites in Victoria, New South Wales, South Australia and Queensland. Its distribution and abundance has been much depleted by loss of habitat, in New South Wales most communities where it occurs are listed as threatened with more than a 50% of population reduction and in Victoria its total area of occupancy is 1.64 km2. The main identified threats to Slender Darling-pea include: grazing pressure, loss of habitat, weed invasion, increased salination, frequency of fires and urban development. According to the NSW Scientific Committee (2009) this species meets the IUCN criteria A3c for Vulnerable. Further research is recommended to determine total population size and impacts from threats. Recent unreported sightings suggest that this species might be relatively common especially after rain (Benson 2010 pers. comm.). Reason(s) for Change in Red List Category from the Previous Assessment: Genuine Change Nongenuine Change No Change Genuine (recent) New information Taxonomy Same category Genuine (since first assessment) Knowledge of Criteria Criteria Revisio and criteria Incorrect data used Other Same category but previously change in criteria Current Population Trend: Decreasing Date of Assessment: 31/08/2010 Name(s) of the Assessor(s): Malcolm, P. Evaluator(s): Notes: % population decline in the past: Time period over which the past decline has been measured for applying Criterion A or C1 (in years or generations): % population decline in the future: Time period over which the future decline has been measured for applying Criterion A or C1 (in years or generations): Number of Locations: Severely Fragmented: Number of Mature Individuals:
Recommended publications
  • 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.
    [Show full text]
  • 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.
    [Show full text]
  • 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.
    [Show full text]
  • 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.
    [Show full text]
  • 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.
    [Show full text]
  • 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.
    [Show full text]
  • Nuytsia the Journal of the Western Australian Herbarium 23: 1–4 Published Online 8 February 2013
    R.W. Davis & P.J.H. Hurter, Swainsona thompsoniana (Fabaceae), a new species from the Pilbara 1 Nuytsia The journal of the Western Australian Herbarium 23: 1–4 Published online 8 February 2013 Swainsona thompsoniana (Fabaceae: Faboideae: Galegeae), a new species endemic to the Pilbara bioregion of Western Australia Robert W. Davis1 and P. Johan H. Hurter2 1Western Australian Herbarium, Department of Environment and Conservation, Locked Bag 104, Bentley Delivery Centre, Western Australia 6983 2GHD, 239 Adelaide Terrace, Perth, Western Australia 6004 1Corresponding author, email: [email protected] Abstract Davis, R.W. & Hurter, P.J.H. Swainsona thompsoniana (Fabaceae: Faboideae: Galegeae), a new species endemic to the Pilbara bioregion of Western Australia. Nuytsia 23: 1–4 (2013). Swainsona thompsoniana R.W.Davis & P.J.H.Hurter is described here as new. An amendment to an existing key for Swainsona Salisb. is provided to account for S. thompsoniana. Swainsona thompsoniana occurs on cracking clay soils from east of Pannawonica to Mount Florence Station and south-east to Tom Price and Wittenoom; a distribution map is included. Introduction Swainsona Salisb. is a relatively large genus of approximately 70 taxa endemic to Australia, 47 of which occur in Western Australia. The genus consists mostly of annual and perennial herbs which are predominately found in the drier regions of central Australia. The last revision of the genus was carried out by Joy Thompson (1993), wherein she described 16 new taxa. Although the new species described herein—S. thompsoniana R.W.Davis & P.J.H.Hurter—was informally named in 1996 as Swainsona sp.
    [Show full text]
  • Fabaceae) Inferred from Nrdna ITS and Two Cpdnas, Matk and Rpl32-Trnl(UAG) Sequences Data
    Plant Biosystems - An International Journal Dealing with all Aspects of Plant Biology Official Journal of the Societa Botanica Italiana ISSN: 1126-3504 (Print) 1724-5575 (Online) Journal homepage: http://www.tandfonline.com/loi/tplb20 Phylogeny and divergence times of the Coluteoid clade with special reference to Colutea (Fabaceae) inferred from nrDNA ITS and two cpDNAs, matK and rpl32-trnL(UAG) sequences data M. Moghaddam, S. Kazempour Osaloo, H. Hosseiny & F. Azimi To cite this article: M. Moghaddam, S. Kazempour Osaloo, H. Hosseiny & F. Azimi (2016): Phylogeny and divergence times of the Coluteoid clade with special reference to Colutea (Fabaceae) inferred from nrDNA ITS and two cpDNAs, matK and rpl32-trnL(UAG) sequences data, Plant Biosystems - An International Journal Dealing with all Aspects of Plant Biology, DOI: 10.1080/11263504.2016.1244120 To link to this article: http://dx.doi.org/10.1080/11263504.2016.1244120 Published online: 19 Oct 2016. Submit your article to this journal Article views: 7 View related articles View Crossmark data Full Terms & Conditions of access and use can be found at http://www.tandfonline.com/action/journalInformation?journalCode=tplb20 Download by: [Cornell University Library] Date: 30 October 2016, At: 10:43 Plant Biosystems, 2016 http://dx.doi.org/10.1080/11263504.2016.1244120 Phylogeny and divergence times of the Coluteoid clade with special reference to Colutea (Fabaceae) inferred from nrDNA ITS and two cpDNAs, matK and rpl32-trnL(UAG) sequences data M. MOGHADDAM1, S. KAZEMPOUR OSALOO1, H. HOSSEINY1, & F. AZIMI2 1Department of Plant Biology, Faculty of Biological Sciences, Tarbiat Modares University, Iran and 2Natural Resource Research Center of Ardabil Province, Iran Abstract This study reconstructed the phylogeny of the Coluteoid clade using nrDNA ITS and plastid matK and rpl32-trnL(UAG) sequences data.
    [Show full text]
  • Silky Swainson-Pea
    NSW SCIENTIFIC COMMITTEE Swainsona sericea (A.T. Lee) J.M. Black ex H. Eichler (Fabaceae-Faboideae) Review of Current Information in NSW June 2008 Current status: Swainsona sericea (Silky Swainson-pea) is currently listed as Threatened in Victoria under the Flora & Fauna Guarantee Act 1988 (FFG Act) and Endangered in South Australia under the National Parks and Wildlife Act 1972 (NPW Act), but is not listed under Commonwealth legislation. The NSW Scientific Committee recently determined that Swainsona sericea meets criteria for listing as Vulnerable in NSW under the Threatened Species Conservation Act 1995 (TSC Act), based on information contained in this report and other information available for the species. Species description: Thompson and James (2002, p. 604) describe Swainsona sericea as follows: “Prostrate or low- growing perennial to about 10 cm high; stems densely pubescent with medifixed hairs, hairs appressed or with both ends raised. Leaves mostly 2-7 cm long; leaflets 5-13, narrow-elliptic, lateral leaflets mostly 5-15 mm long, 1-3 mm wide; terminal leaflets distinctly longer than laterals, apex acute, both surfaces ± pubescent; stipules 3-7 mm long. Racemes mostly 2-8- flowered; flowers 7-11 mm long. Calyx pubescent often with dark hairs, teeth ± equal to the tube. Corolla purple; keel apex obtuse with swellings behind tip, slightly twisted. Style tip geniculate. Pod obovate, usually 10-17 mm long, pubescent; style 6-7 mm long; stipe minute.” Taxonomy: Swainsona sericea was originally described as Swainsona oroboides F. Muell. ex Benth. subsp. sericea A.T. Lee (Eichler 1965). The taxon is now recognised as a true species in all the taxonomic literature.
    [Show full text]
  • Coast Or Purple Swainson-Pea Swainsona Lessertiifolia
    Plant of the month: Coast or Purple Swainson-pea Swainsona lessertiifolia Coast Swainson-pea Swainsona lessertiifolia is a sprawling or scrambling perennial herb growing 10- 50 cm high and up to 1 m wide. The dark green pinnate or divided leaves have 13-21 oblong leaflets that are notched at the tip, smooth above and softly hairy below. The spikes of rich purple (a rare white-flowered form has been found at Venus Bay) pea flowers have a whitish mark at the base and occur mainly from June to January. The oblong pod contains up to 20 seeds. As indicated by its name, Coast Swainson-pea is found in coastal dune communities and tolerates calcareous (lime) soils, drought and salt spray, making it a useful ground cover for Venus Bay gardens. It needs to be hard pruned in winter to encourage vigorous new growth and flowering. Propagation is from scarified or heat treated seed, as for most plants in the pea family. The plant can be distinguished from the similar weed species Vetch by the lack of a tendril at the end of the leaflets. Coast Swainson-pea belongs to the Fabaceae or pea family; the five-petalled flowers are readily identifiable with their large upright standard, two wings and a central keel which is actually two petals fused on the upper edge. The genus Swainsona is named after English botanist Isaac Swainson and the species name lessertiifolia is named for its similarity to the South African species Lessertia perennans. For further information please visit FVBP website above. Photo: Lorraine Norden.
    [Show full text]
  • Wojciechowski Quark
    Wojciechowski, M.F. (2003). Reconstructing the phylogeny of legumes (Leguminosae): an early 21st century perspective In: B.B. Klitgaard and A. Bruneau (editors). Advances in Legume Systematics, part 10, Higher Level Systematics, pp. 5–35. Royal Botanic Gardens, Kew. RECONSTRUCTING THE PHYLOGENY OF LEGUMES (LEGUMINOSAE): AN EARLY 21ST CENTURY PERSPECTIVE MARTIN F. WOJCIECHOWSKI Department of Plant Biology, Arizona State University, Tempe, Arizona 85287 USA Abstract Elucidating the phylogenetic relationships of the legumes is essential for understanding the evolutionary history of events that underlie the origin and diversification of this family of ecologically and economically important flowering plants. In the ten years since the Third International Legume Conference (1992), the study of legume phylogeny using molecular data has advanced from a few tentative inferences based on relatively few, small datasets into an era of large, increasingly multiple gene analyses that provide greater resolution and confidence, as well as a few surprises. Reconstructing the phylogeny of the Leguminosae and its close relatives will further advance our knowledge of legume biology and facilitate comparative studies of plant structure and development, plant-animal interactions, plant-microbial symbiosis, and genome structure and dynamics. Phylogenetic relationships of Leguminosae — what has been accomplished since ILC-3? The Leguminosae (Fabaceae), with approximately 720 genera and more than 18,000 species worldwide (Lewis et al., in press) is the third largest family of flowering plants (Mabberley, 1997). Although greater in terms of the diversity of forms and number of habitats in which they reside, the family is second only perhaps to Poaceae (the grasses) in its agricultural and economic importance, and includes species used for foods, oils, fibre, fuel, timber, medicinals, numerous chemicals, cultivated horticultural varieties, and soil enrichment.
    [Show full text]
  • Floral Development and Breeding System of Swainsona Formosa
    HORTSCIENCE 29(2):117–119. 1994. was horizontal; G = the flag had fully reflexed and the flower was open. Flowers at each developmental stage were harvested and dis- Floral Development and Breeding sected to relate the development of internal System of Swainsona formosa parts to that of the whole flower. (Leguminosae) Results and Discussion Because of the difficulty of finding flowers Manfred Jusaitis developing in synchrony, floral stage and pe- Black Hill Flora Centre, Botanic Gardens of Adelaide, Maryvale Road, duncle length for asynchronous flowers were plotted such that onset of stage G for each Athelstone, South Australia, 5076 flower coincided. This enabled means of syn- Additional index words. Sturt’s desert pea, Clianthus formosus, stigma, pollen germination, chronized floral stages (mean of five flowers) and peduncle lengths (mean of 12 flowers) to be pollination graphed. Peduncle length followed a sigmoidal Abstract. Flowers of Swainsona formosa (G. Don) J. Thompson (syn. Clianthus formosus) growth pattern over the period of floral devel- developed through seven floral stages from buds to open flowers in 17 days. Floral stages opment, with maximal length being attained by were correlated with the sigmoidal growth pattern of the peduncle. Self-pollination was 19 to 20 days (Fig. 2). Flowers remained at prevented in the species by the presence of a stigmatic cuticle that precluded pollen stage A during the first half of this period, but germination until ruptured, exposing the receptive surface below. Cuticular rupture when peduncle growth became linear (day 9), occurred in nature during bird-pollination and was emulated manually by lightly rubbing floral development accelerated quickly through a pollen-covered finger across the stigma.
    [Show full text]