Native Vascular Plant Taxa SWAFR
Total Page：16
File Type：pdf, Size：1020Kb
Load more
Recommended publications
-
Proteaceae Conospermum Caeruleum Subsp. Caeruleum Adj Adj Proteaceae Conospermum Petiolare Proteaceae Conospermum Sericeum
Proteaceae Conospermum caeruleum subsp. Adj Adj caeruleum Proteaceae Conospermum petiolare Proteaceae Conospermum sericeum Haemodoraceae Conostylis setigera X X X X X X X X X Cyperaceae Cyathochaeta avenacea Adj Adj X Cyperaceae Cyathochaeta equitans Goodeniaceae Dampiera juncea X X X X X X Goodeniaceae Dampiera linearis Adj X X X Myrtaceae Darwinia vestita Adj Dasypogonaceae Dasypogon bromeliifolius X X X Fabaceae Daviesia incrassata X X Fabaceae Daviesia alternifolia Fabaceae Daviesia flexuosa Fabaceae Daviesia spinosissima Restionaceae Desmocladus fascicularis X X X X X Restionaceae Desmocladus flexuosus X X Droseraceae Drosera scorpioides X Droseraceae Drosera ? Subhirtella X X Droseraceae Drosera erythrorhiza Droseraceae Drosera ramellosa Droseraceae Drosera sp. (insufficient material) X Droseraceae Drosera stolonifera X X X X Poaceae Eragrostis curvula * Myrtaceae Eucalyptus staeri X X X X Adj X X X X Myrtaceae Eucalyptus decurva Myrtaceae Eucalyptus marginata intergrades with E. staeri Cyperaceae Ficinia nodosa Adj Fabaceae Gastrolobium bracteolosum Adj X X X X Fabaceae Gastrolobium retusum X X Iridaceae Gladiolus sp. * Adj Fabaceae Gompholobium knightianum Adj X Fabaceae Gompholobium marginatum X Fabaceae Gompholobium ovatum Adj Fabaceae Gompholobium polymorphum X X X Fabaceae Gompholobium burtonioides Fabaceae Gompholobium confertum Fabaceae Gompholobium venustum Fabaceae Gompholobium villosum Haloragaceae Gonocarpus trichostachyus P3 Proteaceae Grevillea fasciculata Adj X X Adj X X Haemodoraceae Haemodorum spicatum X Haemodoraceae -
FINAL REPORT 2019 Canna Reserve
FINAL REPORT 2019 Canna Reserve This project was supported by NACC NRM and the Shire of Morawa through funding from the Australian Government’s National Landcare Program Canna Reserve BioBlitz 2019 Weaving and wonder in the wilderness! The weather may have been hot and dry, but that didn’t stop everyone having fun and learning about the rich biodiversity and conservation value of the wonderful Canna Reserve during the highly successful 2019 BioBlitz. On the 14 - 15 September 2019, NACC NRM together with support from Department of Biodiversity Conservation and Attractions and the Shire of Morawa, hosted their third BioBlitz at the Canna Reserve in the Shire of Morawa. Fifty professional biologists and citizen scientists attended the event with people travelling from near and far including Morawa, Perenjori, Geraldton and Perth. After an introduction and Acknowledgement of Country from organisers Jessica Stingemore and Jarna Kendle, the BioBlitz kicked off with participants separating into four teams and heading out to explore Canna Reserve with the goal of identifying as many plants, birds, invertebrates, and vertebrates as possible in a 24 hr period. David Knowles of Spineless Wonders led the invertebrate survey with assistance from, OAM recipient Allen Sundholm, Jenny Borger of Jenny Borger Botanical Consultancy led the plant team, BirdLife Midwest member Alice Bishop guided the bird survey team and David Pongracz from Department of Biodiversity Conservation and Attractions ran the vertebrate surveys with assistance from volunteer Corin Desmond. The BioBlitz got off to a great start identifying 80 plant species during the first survey with many more species to come and even a new orchid find for the reserve. -
Download a Brochure on Eco Trails Walks in the Shire of Moora
Walks in the Shire of Moora Eco Trails Come Explore Moore Front cover: Moora Carnaby’s Black Cockatoo walk trail Inside front: Wheatbin Road Reserve/Old Reserve, Moora Inside back: Candy’s Bush Reserve, Moora Back cover: Price’s Road wildflowers Welcome to Walks When exploring the bush remember to: in the Shire of Moora Be sun smart. Cover up, wear a hat, and take plenty of water. The Shire of Moora is situated This differing geology has led to two Wear good shoes which enclose feet. approximately 2hrs north of Perth very different botanical districts with and features a wonderful array of the Shire of Moora being home to 2364 remnant native vegetation amongst species of plants and animals. The the Wheatbelt arable landscape. Stay towering Salmon Gums and Wandoo a-while and explore Moore ! trees are iconic of the eastern Shire Watch for snakes Leave only footprints, Geologically, the Shire features two whilst heading west takes you in to the colourful Banksia woodland and (Dugites & Western take only photographs. main distinct soil types separated by the Browns especially) and It is illegal to remove any Kwongan heathlands. The endangered Darling Fault. This fault runs north-south other potentially harmful native flora and fauna. through Moora and is marked by the Carnaby’s Black Cockatoo can be seen in animals. Watch out for course of the Moore River. To the east the western half of the Shire utilising the broken glass and dumped lies very ancient (over 2 billion years remaining native vegetation as breeding rubbish. Carry a 1st aid kit. -
Origin and Age of Australian Chenopodiaceae
ARTICLE IN PRESS Organisms, Diversity & Evolution 5 (2005) 59–80 www.elsevier.de/ode Origin and age of Australian Chenopodiaceae Gudrun Kadereita,Ã, DietrichGotzek b, Surrey Jacobsc, Helmut Freitagd aInstitut fu¨r Spezielle Botanik und Botanischer Garten, Johannes Gutenberg-Universita¨t Mainz, D-55099 Mainz, Germany bDepartment of Genetics, University of Georgia, Athens, GA 30602, USA cRoyal Botanic Gardens, Sydney, Australia dArbeitsgruppe Systematik und Morphologie der Pflanzen, Universita¨t Kassel, D-34109 Kassel, Germany Received 20 May 2004; accepted 31 July 2004 Abstract We studied the age, origins, and possible routes of colonization of the Australian Chenopodiaceae. Using a previously published rbcL phylogeny of the Amaranthaceae–Chenopodiaceae alliance (Kadereit et al. 2003) and new ITS phylogenies of the Camphorosmeae and Salicornieae, we conclude that Australia has been reached in at least nine independent colonization events: four in the Chenopodioideae, two in the Salicornieae, and one each in the Camphorosmeae, Suaedeae, and Salsoleae. Where feasible, we used molecular clock estimates to date the ages of the respective lineages. The two oldest lineages both belong to the Chenopodioideae (Scleroblitum and Chenopodium sect. Orthosporum/Dysphania) and date to 42.2–26.0 and 16.1–9.9 Mya, respectively. Most lineages (Australian Camphorosmeae, the Halosarcia lineage in the Salicornieae, Sarcocornia, Chenopodium subg. Chenopodium/Rhagodia, and Atriplex) arrived in Australia during the late Miocene to Pliocene when aridification and increasing salinity changed the landscape of many parts of the continent. The Australian Camphorosmeae and Salicornieae diversified rapidly after their arrival. The molecular-clock results clearly reject the hypothesis of an autochthonous stock of Chenopodiaceae dating back to Gondwanan times. -
Structural Botany / Botánica Estructural
Botanical Sciences 99(3): 588-598. 2021 Received: October 15, 2020, Accepted: December 1, 2020 DOI: 10.17129/botsci.2776 AcaciaOn linecornigera first: April 15, 2021 Structural Botany / Botánica Estructural FLORAL DEVELOPMENT OF THE MYRMECOPHYTIC ACACIA CORNIGERA (LEGUMINOSAE) DESARROLLO FLORAL DE LA MIRMECÓFITA ACACIA CORNIGERA (LEGUMINOSAE) SANDRA LUZ GÓMEZ-ACEVEDO1,2 1 Unidad de Morfología y Función. Facultad de Estudios Superiores Iztacala, Universidad Nacional Autónoma de México, Tlalnepantla, Estado de México, México. 2 Departamento de Ecología Evolutiva, Instituto de Ecología, Universidad Nacional Autónoma de México, CDMX, México. Author for correspondence: [email protected] Abstract Background: The Neotropical ant-acacias show morphological variations in their vegetative characteristics as a consequence of their relation- ship with ants. However, there is no information regarding whether floral organs have also undergone any modification that prevents resident ants from approaching the inflorescences in anthesis. Questions: Are the patterns of floral development affected by the relationship with ants? Is there any floral organ or structure involved in avoid- ing the presence of ants during the flowering period? At what stage of development do these modifications arise, if at all? Studied species: Acacia cornigera (L.) Willd. Study site: Santiago Pinotepa Nacional, Oaxaca and Los Tuxtlas, Veracruz. March and May 2015. Methods: Dissections of inflorescences in every developmental stage from two populations, were examined using scanning electron micros- copy. Results: The inception patterns of the calyx (irregular), corolla (simultaneous), androecium (acropetally in alternate sectors) and gynoecium (precocious) agree with previous reports for non-myrmecophyic species of the Acacia genus. In mature stages, the presence of stomata is char- acteristic of bracts and petals. -
Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- BIBLIOGRAPHY
Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- BIBLIOGRAPHY BIBLIOGRAPHY Ackerfield, J., and J. Wen. 2002. A morphometric analysis of Hedera L. (the ivy genus, Araliaceae) and its taxonomic implications. Adansonia 24: 197-212. Adams, P. 1961. Observations on the Sagittaria subulata complex. Rhodora 63: 247-265. Adams, R.M. II, and W.J. Dress. 1982. Nodding Lilium species of eastern North America (Liliaceae). Baileya 21: 165-188. Adams, R.P. 1986. Geographic variation in Juniperus silicicola and J. virginiana of the Southeastern United States: multivariant analyses of morphology and terpenoids. Taxon 35: 31-75. ------. 1995. Revisionary study of Caribbean species of Juniperus (Cupressaceae). Phytologia 78: 134-150. ------, and T. Demeke. 1993. Systematic relationships in Juniperus based on random amplified polymorphic DNAs (RAPDs). Taxon 42: 553-571. Adams, W.P. 1957. A revision of the genus Ascyrum (Hypericaceae). Rhodora 59: 73-95. ------. 1962. Studies in the Guttiferae. I. A synopsis of Hypericum section Myriandra. Contr. Gray Herbarium Harv. 182: 1-51. ------, and N.K.B. Robson. 1961. A re-evaluation of the generic status of Ascyrum and Crookea (Guttiferae). Rhodora 63: 10-16. Adams, W.P. 1973. Clusiaceae of the southeastern United States. J. Elisha Mitchell Sci. Soc. 89: 62-71. Adler, L. 1999. Polygonum perfoliatum (mile-a-minute weed). Chinquapin 7: 4. Aedo, C., J.J. Aldasoro, and C. Navarro. 1998. Taxonomic revision of Geranium sections Batrachioidea and Divaricata (Geraniaceae). Ann. Missouri Bot. Gard. 85: 594-630. Affolter, J.M. 1985. A monograph of the genus Lilaeopsis (Umbelliferae). Systematic Bot. Monographs 6. Ahles, H.E., and A.E. -
Acacia in THIS ISSUE Dacacia the Name Acacia Comes This Issue of Seed Notes from the Greek Acacia, Ace Will Cover the Genus Or Acis Meaning a Point Or Acacia
No. 9 Acacia IN THIS ISSUE DAcacia The name Acacia comes This issue of Seed Notes from the Greek acacia, ace will cover the genus or acis meaning a point or Acacia. thorn, or from acazo, to D Description sharpen, although this name applies more to African than D Geographic Australian species (Australian distribution and Acacia have no thorns or habitat larger prickles, unlike those D Reproductive biology that are native to Africa). D Seed collection Many species of Acacia, or wattles as they are commonly D Phyllodes and flowers of Acacia aprica. Photo – Andrew Crawford Seed quality called in Australia, are valuable assessment for a range of uses, in D Seed germination particular as garden plants. Description In Australia, Acacia (family is modified to form a leaf- D Recommended reading They are also used for amenity plantings, windbreaks, shade DMimosaceae) are woody like structure or phyllode. trees, groundcovers, erosion plants that range from These phyllodes may be flat and salinity control. The timber prostrate under-shrubs to or terete. Some species do of some Acacia is very hard tall trees. Acacia flowers are not have phyllodes and the and is ideal for fence posts small, regular and usually flattened stems or cladodes (e.g. A. saligna or jam). Other bisexual. They occur in spikes act as leaves. Foliage can Acacia species are used to or in globular heads and vary from blueish to dark make furniture and ornaments. range in colour from cream green to silvery grey. Most The seed of some wattles is to intense yellow. The leaves species of Acacia have glands a good food source for birds, of Acacia may be bipinnate on the axis of the phyllodes, other animals and humans (the primary leaflets being although in Australian as ‘bush tucker’. -
Acacia Bifaria Maslin
WATTLE Acacias of Australia Acacia bifaria Maslin Source: Australian Plant Image Index Source: Australian Plant Image Index (dig.949). Source: Australian Plant Image Index (dig.950). (dig.16967). ANBG © M. Fagg, 2005 ANBG © M. Fagg, 2005 ANBG © M. Fagg, 2010 Source: Australian Plant Image Index (a.30952). ANBG © M. Fagg, 2002 Source: W orldW ideW attle ver. 2. Published at: w w w .w orldw idew attle.com Acacia bifaria occurrence map. O ccurrence map generated via Atlas of Living Australia (https://w w w .ala.org.au). Family Fabaceae Distribution Occurs from Ravensthorpe WSW to the Fitzgerald R. (c. 30 km due E of Jerramungup), south-western W.A. Description Prostrate or semi-prostrate shrub to 0.5 m high and 2 m across. Branchlets slightly to prominently flexuose, glabrous. Stipules persistent. Phyllodes continuous with branchlets, bifariously decurrent and forming opposite wings with each one extending to the next below, 1–3.5 cm long, 4–10 mm wide, coriaceous, green to subglaucous, glabrous except axils densely and minutely resin-haired; margins occasionally undulate; free portion of phyllode with obviously rounded adaxial margin, 5–15 mm long, excentrically mucronate, with main nerve ±obscure or superficially absent; gland not prominent. Inflorescences rudimentary, 1-headed racemes with axes 0.5–1.5 mm long; peduncles 2–12 mm long, glabrous, sometimes descending in fruit; heads globular, 16–23-flowered, light golden. Flowers 5-merous; sepals ±free; petals nerveless. Pods strongly curved to twice-coiled, ±terete, to 2 cm long, 2–3 mm wide, thinly crustaceous, black, ±glabrous. Seeds longitudinal, oblong, c. -
Conservation Advice Acacia Subflexuosa Subsp. Capillata
THREATENED SPECIES SCIENTIFIC COMMITTEE Established under the Environment Protection and Biodiversity Conservation Act 1999 The Minister’s delegate approved this conservation advice on 01/10/2015 Conservation Advice Acacia subflexuosa subsp. capillata hairy-stemmed zig-zag wattle Conservation Status Acacia subflexuosa subsp. capillata (hairy-stemmed zig-zag wattle) is listed as Endangered under the Environment Protection and Biodiversity Conservation Act 1999 (Cwlth) (EPBC Act). The species is eligible for listing as endangered as, prior to the commencement of the EPBC Act, it was listed as endangered under Schedule 1 of the Endangered Species Protection Act 1992 (Cwlth). The main factors that are the cause of the species being eligible for listing in the endangered category are a restricted extent of occurrence and a low number of mature individuals (Harris and Brown, 2003). In 1998, the subspecies was listed as Rare Flora and Critically Endangered in Western Australia (Wildlife Conservation Act 1950). Description The hairy-stemmed zig-zag wattle is a rounded shrub (Brown et al., 1998) to 1 m tall with thickened, sharply-pointed phyllodes, 3 to 4 cm long and 1 to 1.5 mm wide (Harris and Brown, 2003). Flowers are in yellow globular heads (Orchard and Wilson, 2001), on 4 to 6 mm long stalks and appear from August to November (Brown et al., 1998; Cowan & Maslin 1999). Pods are narrow and coiled, 4 cm long and 2 mm wide. Distribution The hairy-stemmed zig-zag wattle is endemic to the Cunderdin-Tammin area of Western Australia where it occurs over a range of less than 5 km (Orchard and Wilson, 2001). -
State-Wide Seed Conservation Strategy for Threatened Species, Threatened Communities and Biodiversity Hotspots
State-wide seed conservation strategy for threatened species, threatened communities and biodiversity hotspots Project 033146a Final Report South Coast Natural Resource Management Inc. and Australian Government Natural Heritage Trust July 2008 Prepared by Anne Cochrane Threatened Flora Seed Centre Department of Environment and Conservation Western Australian Herbarium Kensington Western Australia 6983 Summary In 2005 the South Coast Natural Resource Management Inc. secured regional competitive component funding from the Australian Government’s Natural Heritage Trust for a three-year project for the Western Australian Department of Environment and Conservation (DEC) to coordinate seed conservation activities for listed threatened species and ecological communities and for Commonwealth identified national biodiversity hotspots in Western Australia (Project 033146). This project implemented an integrated and consistent approach to collecting seeds of threatened and other flora across all regions in Western Australia. The project expanded existing seed conservation activities thereby contributing to Western Australian plant conservation and recovery programs. The primary goal of the project was to increase the level of protection of native flora by obtaining seeds for long term conservation of 300 species. The project was successful and 571 collections were made. The project achieved its goals by using existing skills, data, centralised seed banking facilities and international partnerships that the DEC’s Threatened Flora Seed Centre already had in place. In addition to storage of seeds at the Threatened Flora Seed Centre, 199 duplicate samples were dispatched under a global seed conservation partnership to the Millennium Seed Bank in the UK for further safe-keeping. Herbarium voucher specimens for each collection have been lodged with the State herbarium in Perth, Western Australia. -
Kalannie Region
Botanical name Acacia daphnifolia Meisn. Synonym: microbotrya var. borealis E. Pritzel, Bot. Jahrb. Syst. 35: 300 (1904). Common name Northern Manna Wattle. Characteristic features Bushy shrubs or small trees, often forming dense clonal clumps by root suckers. Phyllodes normally oblanceolate, straight to shallowly falcately recurved, widely spreading, glaucous to sub-glaucous, with one longitudinal nerve on each face, apices obtuse to acute (sometimes acuminate); glands normally single (rarely 2). Heads globular, showy, arranged in short racemes, the raceme axes and peduncles appressed hairy. Pods moniliform to sub-moniliform, 7-8 mm wide. Seeds large; funicle encircling seeds in a single fold and drying red- brown. Flowering around autumn. Description Note. Acacia microbotyra is a somewhat variable species and is in need of critical revision. The description here applies only to plants occurring within the Kalannie region. Habit. Bushy, +/- rounded shrubs or +/- obconic small trees mostly 2-4 m tall with crowns 2-5 m across, often forming dense clonal clumps by root suckers, dividing at ground level into 2-4 main trunks (6-9 cm in diameter at breast height) or with a single trunk (about 11 cm diameter at ground level) to about 1 m before branching, crowns on oldest plants occupying 20-30% of the total plant height, Bark. Grey, thin and hard, shallowly longitudinally fissured with fine transverse fractures, exfoliating in short strips on oldest trunks, smooth on upper branches. Gum. Sometimes exuded from the trunks and/or branches. Branchlets. -
Report Nnual
DEPARTMENT OF CONSERVATION AND LAND MANAGEMENT nnual eport A R 2002-2003 HIGHLIGHTS OF THE YEAR Our Vision Our Principles Our Responsibilities A natural environment In making decisions we will be guided The Department of Conservation and in Western Australia that by the following principles: Land Management is part of a greater retains its biodiversity and • The diversity and health of ecological conservation community and has enriches people’s lives. communities and native species distinct State Government throughout WA will be maintained responsibilities for implementing and restored. Government policy within that • Where there are threats of serious or community. Conservation is a irreversible damage, the lack of full collective role. scientific certainty shall not be used Our Mission as a reason for postponing measures We have the lead responsibility for which seek to prevent loss of conserving the State’s rich diversity of In partnership with the community, biodiversity. native plants, animals and natural we conserve Western Australia’s • Users of the environment and ecosystems, and many of its unique biodiversity, and manage the lands resources will pay fair value for that landscapes. On behalf of the people of use. and waters entrusted to us, for their Western Australia, we manage more • Use of wildlife will be on the basis of than 24 million hectares, including intrinsic values and for the ecological sustainability. more than 9 per cent of WA’s land area: appreciation and benefit of present • Outcomes will be delivered in the most its national parks, marine parks, and future generations. effective and efficient way. conservation parks, regional parks, • Cooperation, sharing and integration State forests and timber reserves, of resources and knowledge within the nature reserves, and marine nature Department and between reserves.