Descriptions in the Literature of the Colour in Trees from Southwest Australia
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Banksia Vincentia (Proteaceae), a New Species Known from Fourteen Plants from South-Eastern New South Wales, Australia
Phytotaxa 163 (5): 269–286 ISSN 1179-3155 (print edition) www.mapress.com/phytotaxa/ Article PHYTOTAXA Copyright © 2014 Magnolia Press ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.163.5.3 Could this be Australia’s rarest Banksia? Banksia vincentia (Proteaceae), a new species known from fourteen plants from south-eastern New South Wales, Australia MARGARET L. STIMPSON1, JEREMY J. BRUHL1 & PETER H. WESTON2 1 Botany, School of Environmental and Rural Science, University of New England, Armidale NSW 2351 Australia Corresponding Author Email: [email protected] 2 National Herbarium of New South Wales, Royal Botanic Garden Sydney, Mrs Macquaries Road, Sydney, NSW 2000, Australia Abstract Possession of hooked, distinctively discolorous styles, a broadly flabellate common bract subtending each flower pair, and a lignotuber place a putative new species, Banksia sp. Jervis Bay, in the B. spinulosa complex. Phenetic analysis of individuals from all named taxa in the B. spinulosa complex, including B. sp. Jervis Bay, based on leaf, floral, seed and bract characters support recognition of this species, which is described here as Banksia vincentia M.L.Stimpson & P.H.Weston. Known only from fourteen individuals, B. vincentia is distinguished by its semi-prostrate habit, with basally prostrate, distally ascending branches from the lignotuber, and distinctive perianth colouring. Its geographical location and ecological niche also separate it from its most similar congeners. Introduction The Banksia spinulosa complex has a complicated taxonomic history (Table 1). Smith (1793) first described and named B. spinulosa Sm., and subsequent botanists named two close relatives, B. collina R.Br. and B. -
List of Plants Used by Carnaby's Black Cockatoo
Plants Used by Carnaby's Black Cockatoo List prepared by Christine Groom, Department of Environment and Conservation 15 April 2011 For more information on plant selection or references used to produce this list please visit the Plants for Carnaby's Search Tool webpage at www.dec.wa.gov.au/plantsforcarnabys Used for Soil type Soil drainage Priority for planting Sun Species Growth form Flower colour Origin for exposure Carnaby's Feeding Nesting Roosting Clayey Gravelly Loamy Sandy drained Well drained Poorly Waterlogged affected Salt Acacia baileyana (Cootamundra wattle)* Low Tree Yellow Australian native Acacia pentadenia (Karri Wattle) Low Tree Cream WA native Acacia saligna (Orange Wattle) Low Tree Yellow WA native Agonis flexuosa (Peppermint Tree) Low Tree White WA native Araucaria heterophylla (Norfolk Island Pine) Low Tree Green Exotic to Australia Banksia ashbyi (Ashby's Banksia) Medium Tree or Tall shrub Yellow, Orange WA native Banksia attenuata (Slender Banksia) High Tree Yellow WA native Banksia baxteri (Baxter's Banksia) Medium Tall shrub Yellow WA native Banksia carlinoides (Pink Dryandra) Medium Medium or small shrub White, cream, pink WA native Banksia coccinea (Scarlet Banksia) Medium Tree Red WA native Banksia dallanneyi (Couch Honeypot Dryandra) Low Medium or small shrub Orange, brown WA native Banksia ericifolia (Heath-leaved Banksia) Medium Tall shrub Orange Australian native Banksia fraseri (Dryandra) Medium Medium or small shrub Orange WA native Banksia gardneri (Prostrate Banksia) Low Medium -
Proteaceae (Banksia Species)
Proteaceae (Banksia Species) Information: 90% of all Banksia species occur in South Western Australia. The two most com- mon Banksia species in the Perth region are the Firewood Banksia (Banksia menziesii) and the Slender or Candle Banksia (Banksia attenuata). These two species each flower throughout the two halves of the year and are an important source of food for countless animals. Large Banksias such as these as well as B. grandis, B. ilicifolia B. Prionotes and B. littoralis produce an abun- dance of nectar from their large flower spikes that sustain countless species and have traditionally been used as a source of food and drink by indigenous Australians. Banksias are highly adapted to a nutrient poor environment with harsh, dry climate having sunken stomata to preserve water and cluster roots to enhance nutrient uptake in Phosphorus deficient soils. Firewood Banksia (Banksia menziesii) with parasitic ’witches broom’ (insert) Pictures by A. Price Candle Banksia (Banksia attenuata) feeding a Honey Possum (Tarsipes rostratus) Picture courtesy of Kwongan Foundation Associated Life: Many animals drink nectar from Banksia flower heads including Perching birds such as Honeyeaters, Spinebills, robins and Wagtails as well as the Honey Possum, the worlds only nectarvorious marsupial. Bull Banksia European Honeybees are commonly (Banksia Grandis) found in or near flower spikes as are wee- vils and jewel beetles. Picture courtesy of Friends of Queens Park Bushland The seeds of the B.grandis are eaten by Carnaby’s black-cockatoo and the red- capped parrot. The Twig-mound ant builds its nest at the base of B. ilicifolia. Some moth species larvae burrow into Banksia cones and leaves. -
Fungal Planet Description Sheets: 558–624
Persoonia 38, 2017: 240–384 ISSN (Online) 1878-9080 www.ingentaconnect.com/content/nhn/pimj RESEARCH ARTICLE https://doi.org/10.3767/003158517X698941 Fungal Planet description sheets: 558–624 P.W. Crous1, M.J. Wingfield 2, T.I. Burgess3, G.E.St.J. Hardy3, P.A. Barber 4, P. Alvarado5, C.W. Barnes 6, P.K. Buchanan7, M. Heykoop8, G. Moreno8, R. Thangavel 9, S. van der Spuy10, A. Barili11, S. Barrett12, S.O. Cacciola13, J.F. Cano-Lira14, C. Crane15, C. Decock16, T.B. Gibertoni17, J. Guarro14, M. Guevara-Suarez14, V. Hubka18, M. Kolařík19, C.R.S. Lira17, M.E. Ordoñez11, M. Padamsee7, L. Ryvarden 20, A.M. Soares17, A.M. Stchigel14, D.A. Sutton21, A. Vizzini 22, B.S. Weir7, K. Acharya 23, F. Aloi13, I.G. Baseia 24, R.A. Blanchette 25, J.J. Bordallo 26, Z. Bratek 27, T. Butler 28, J. Cano-Canals 29, J.R. Carlavilla8, J. Chander 30, R. Cheewangkoon31, R.H.S.F. Cruz 32, M. da Silva 33, A.K. Dutta 23, E. Ercole 34, V. Escobio 35, F. Esteve-Raventós 8, J.A. Flores11, J. Gené14, J.S. Góis24, L. Haines28, B.W. Held 25, M. Horta Jung 36, K. Hosaka 37, T. Jung 36, Ž. Jurjević 38, V. Kautman 39, I. Kautmanova 40, A.A. Kiyashko 41, M. Kozanek 42, A. Kubátová18, M. Lafourcade 43, F. La Spada13, K.P.D. Latha 44, H. Madrid 45, E.F. Malysheva 41, P. Manimohan 44, J.L. Manjón 8, M.P. Martín 46, M. Mata 47, Z. Merényi 27, A. Morte 26, I. -
Registeredqyaustralia Post" . . .• ·.· .. ทท
RegisteredqyAustralia Post" . .• ·.· .. ·· . .·Pr!~tJ>ost Publication Number: PP 545~4.!i - ()005 ISSN 10:,34~121.& .Guymer :.;,· .·:.: .". ·,· . ·.. - '~> _. ·,-· The Society . ~The A:usitalian Syste~atic Botany Soci~ty:isan inc0rpbtated asso~lation ·ofover300peopk~itl} pr9fe.ssi~nal··· . or amateur interest.inl)otany. The !lim ofthe Society is toprcnnoi:e the study of plant systernatics, . - . " . ' ·.~. - : . .. ~ ' . ·Membership. ···Member~hip .is .open to·ailthose intere~ted·in ,plantsysJep1atics, · Membershii)"entitles. tb~.·lllember i:o'attend . ·.. general meetings and:ch:;lptel" meetiugs,ahdto recdve theNewsieiter, Any person may apply formembetshjpby filii rig if1'iln .• ~'Meflibersh1p'Appli~atioi!"forrn an(jfonyfln;iiJ1g: itr.withthe api:n;opriate. subscription, to the treas- .. '.uret .Subsciiptioris becomed~e onJanuary{ea~hyear. · ·. · · · ·· · · · · .-·-- ., ,-_ ·-· -- ··-· ·-- -· -. ·_·.. ·. : ,-. ' The Newsletter '!ppears qlial:tedY ,)eepsmen1l;lers infmrneci of Society events 'and: news' and pr()~ides a ..... ., vehiCle f6r.del:l.ate ancl'discussiori. In addition; origiqal' articles, iroteS arid letters (nOLex'ceedi~gten'publisbed. >pagesil1 Jengt\1) wili be cbrisidere~> .·. .. ' . Gqntribtltions .. sh~uld be. ~ent t~ bne .of the edirod at the address gi v~n ]Jelow, They shovld pref~rably be .. · · submitted.as:~an tli1f()rinah:ed w.orq-pi·ocessor orASCII file on.anMS-D,OS 'or Macinwsli diskette,.accompimied ·. bya printed. topy;:as: an unfonnatted word-proc~ssor or ASCII em::t!L}ile, .atc.on\panied by a·. fax ineSsij.gt; .. ·..• rep,orii~g' tn~. sending of the, file; •or as t~o typed c(ipies=wjth double~spacing 'iflessth<lil one page.' . _:· - ·.,. _-,. - -.. _. ' •. - -.- - . '. .. .. i•. .- ,; ' ---.- " ~- " '.Th~deacihne f6n:ontfibuti6~~ .is the~lqs,t day.'cl.fFebruary, May, Aug~st, ~ndNovehib:er. -
Australian Native Plants Society Australia Hakea
AUSTRALIAN NATIVE PLANTS SOCIETY AUSTRALIA HAKEA STUDY GROUP NEWSLETTER No. 59 OCTOBER 2015 ISSN0727-7008 Leader Paul Kennedy OAM 210 Aireys St. Elliminyt 3250 Tel. 03-52315569 Internet [email protected] Dear members, I apologise for being late with this newsletter, however, my modem ceased operating and it took six weeks to fix. Two of the new modems they sent out did not work and each took eight days to arrive by post. It was very frustrating just when I needed the computer to be operational. The weather here has been very erratic. There was no rain in October until the last day when 18mm fell. There were numerous warm days well above the average and I had to water the smaller plants that had just gone in the ground. Normally we would receive about 100mm for the month. The inland members gardens have been experiencing very dry conditions and the possibility of a very hot summer will see many plants needing the addition of moisture. Outback Queensland in particular is in the throes of a severe drought and the Hakeas from that region such as maconochieana, collina and ivoryi will be greatly stressed as well as being prone to damage from goats. Along the east coast from Gippsland to northern NSW there has been plenty of rain and gardens have been subject to very wet conditions. In Western Australia Jennifer Young has reported that good winter rains have transformed the northern sand plains into a blaze of flowering plants from Exmouth to Kalbarri. Our garden in Colac continues to thrive. -
Seedling Water Stress Response of Two Sandplain Banksia Speciesdiffering
JournalJournal of Mediterranean of Mediterranean Ecology Ecology vol.3, vol.3, No. 4No. 2002: 4 2002 3-9 © Firma Effe Publisher, Reggio Emilia, I Seedling water stress response of two sandplain Banksia species differing in ability to tolerate drought Philip K. Groom Centre for Ecosystem Management, School of Natural Sciences, Edith Cowan University, 100 Joondalup Drive, Joondalup 6027, Western Australia Current contact details: Centre for Horticulture and Plant Sciences, University of Western Sydney, Locked Bag 1797, Penrith South DC, NSW 1797, Australia - Fax: + 61 2 4570 1314 - E-mail: [email protected] Keywords: Banksia, drought tolerance, sandplain, soil moisture content, stomatal conductance, water stress Abstract Effects of water stress on xylem water potential, stomatal conductance and growth were assessed experimentally on 7- month-old seedlings of Banksia menziesii R.Br. (Firewood Banksia) and Banksia littoralis R.Br. (Swamp Banksia) (Pro- teaceae) grown in 1 m deep tubes filled with course sand and subjected to 140 days of drought. Both are tree species of the sandplains of mediterranean southwestern Australia. B. littoralis is restricted to low-lying, winter damp areas, inclu- ding the fringe of seasonal and permanent wetlands, whereas B. menziesii inhabits a range of habitats ranging from mid- upper slopes of deep, sandy dunes to dune crests. It was hypothesised that differences in their water relations and growth responses would reveal drought adaptation attributes that relates to their contrasting habitat preferences. For both spe- cies drought caused significant decreases in stomatal conductance and predawn xylem water potential. B. menziesii seedlings had a low stomatal conductance (< 0.1 mol m-2 s-1) and exhibited a desiccation avoidance response to drought by maintaining relatively higher water potential. -
Sample Chapter
wildflower country DISCOVERING BIODIVERSITY IN AUSTRALIA’S SOUTHWEST wildflower country DISCOVERING BIODIVERSITY IN AUSTRALIA’S SOUTHWEST STANLEY and KAISA BREEDEN fine independent publishing ENDPAPERS: Weathered banksia seed cones on a woodland floor. following pages: White Plume Grevillea, Grevillea leucopteris, is a tall shrub that rises majestically out of low scrubby HALF TITLE: Wreath Flower, Lechenaultia macrantha. heath known as kwongan. The flower spikes grow at the end of PRECEDING PAGE: One-sided Bottlebrush of the genus long slender stems. Calothamnus. Most of the 45 described species of this genus are pages 8–9: Giant Red Tingle, Eucalyptus jacksonii, is one of unique to the Southwest Botanical Province. several forest giants growing in the high rainfall areas of the OPPOSITE: Golden Dryandra, Banksia (Dryandra) nobilis. southwest coast. The dryandras are emblematic of the Province. With nearly 100 Page 11: Fuchsia Grevillea, Grevillea bipinnatifida. species it has great diversity and each one is unique to the region. Mostly an understorey shrub in woodland and forest. The genus Dryandra was merged with Banksia in 2007 (see page 124). First published in 2010 by Fremantle Press 25 Quarry Street, Fremantle, Western Australia 6160 (PO Box 158, North Fremantle, Western Australia 6159) www.fremantlepress.com.au Copyright text © Stan and Kaisa Breeden 2010 Copyright photographs © Stan and Kaisa Breeden 2010 Copyright map © Kaisa Breeden 2010 Copyright foreword © Stephen D. Hopper 2010 This book is copyright. Apart from any fair dealing for the purpose of private study, research, criticism or review, as permitted under the Copyright Act, no part may be reproduced by any process without written permission. -
Flora and Vegetation Of
__________________________________________________________________________________________ FLORA AND VEGETATION OF AVIVA LEASE AREA Prepared for: URS Australia Pty Ltd on behalf of Aviva Corporation Ltd Prepared by: Mattiske Consulting Pty Ltd February 2009 MATTISKE CONSULTING PTY LTD URS0808/195/08 MATTISKE CONSULTING PTY LTD __________________________________________________________________________________________ TABLE OF CONTENTS Page 1. SUMMARY ................................................................................................................................................ 1 2. INTRODUCTION ...................................................................................................................................... 3 2.1 Location .............................................................................................................................................. 3 2.2 Climate ................................................................................................................................................ 3 2.3 Landforms and Soils ........................................................................................................................... 4 2.4 Vegetation ........................................................................................................................................... 4 2.5 Declared Rare, Priority and Threatened Species ................................................................................. 4 2.6 Threatened Ecological Communities (TEC’s) ................................................................................... -
Literaturverzeichnis
Literaturverzeichnis Abaimov, A.P., 2010: Geographical Distribution and Ackerly, D.D., 2009: Evolution, origin and age of Genetics of Siberian Larch Species. In Osawa, A., line ages in the Californian and Mediterranean flo- Zyryanova, O.A., Matsuura, Y., Kajimoto, T. & ras. Journal of Biogeography 36, 1221–1233. Wein, R.W. (eds.), Permafrost Ecosystems. Sibe- Acocks, J.P.H., 1988: Veld Types of South Africa. 3rd rian Larch Forests. Ecological Studies 209, 41–58. Edition. Botanical Research Institute, Pretoria, Abbadie, L., Gignoux, J., Le Roux, X. & Lepage, M. 146 pp. (eds.), 2006: Lamto. Structure, Functioning, and Adam, P., 1990: Saltmarsh Ecology. Cambridge Uni- Dynamics of a Savanna Ecosystem. Ecological Stu- versity Press. Cambridge, 461 pp. dies 179, 415 pp. Adam, P., 1994: Australian Rainforests. Oxford Bio- Abbott, R.J. & Brochmann, C., 2003: History and geography Series No. 6 (Oxford University Press), evolution of the arctic flora: in the footsteps of Eric 308 pp. Hultén. Molecular Ecology 12, 299–313. Adam, P., 1994: Saltmarsh and mangrove. In Groves, Abbott, R.J. & Comes, H.P., 2004: Evolution in the R.H. (ed.), Australian Vegetation. 2nd Edition. Arctic: a phylogeographic analysis of the circu- Cambridge University Press, Melbourne, pp. marctic plant Saxifraga oppositifolia (Purple Saxi- 395–435. frage). New Phytologist 161, 211–224. Adame, M.F., Neil, D., Wright, S.F. & Lovelock, C.E., Abbott, R.J., Chapman, H.M., Crawford, R.M.M. & 2010: Sedimentation within and among mangrove Forbes, D.G., 1995: Molecular diversity and deri- forests along a gradient of geomorphological set- vations of populations of Silene acaulis and Saxi- tings. -
Foliar Nutrient-Allocation Patterns in Banksia Attenuata and Banksia
Foliar nutrient-allocation patterns in Banksia attenuata and Banksia sessilis differing in growth rate and adaptation to low-phosphorus habitats Zhongming Han1, Jianmin Shi2, Jiayin Pang3, Li Yan4, Patrick Finnegan4, and Hans Lambers3 1Jilin Agricultural University 2Jiangxi Agricultural University 3The University of Western Australia 4University of Western Australia June 24, 2020 Abstract We compared the use of phosphorus (P) and nitrogen (N) in slow-growing Banksia attenuata (Proteaceae), which resprouts after fire and naturally occurs on deep sand, with faster-growing opportunistic B. sessilis, which is killed by fire and occurs on shallow sand over laterite or limestone. We carried out pot experiments with plants on substrates with different P availability. We measured foliar nutrient concentrations, and P allocated to major biochemical fractions. The two species had similar foliar total P concentrations, but distinct patterns of P allocation to P-containing fractions. The foliar total N concentration of B. sessilis was greater than that of B. attenuata on all substrates. The foliar total P and N concentrations in both species decreased with decreasing P availability. The relative growth rate of both species was positively correlated with both foliar nucleic acid P and total N concentrations, but there was no correlation with other P and N fractions. Faster-growing B. sessilis allocated more P to nucleic acids than B. attenuata did, but other fractions were similar. We conclude that the nutrient-allocation patterns in faster-growing opportunistic B. sessilis and slower-growing B. attenuata revealed different strategies in response to soil P availability, which matched their contrasting growth strategy. INTRODUCTION Understanding strategies of nutrient allocation and their underlying mechanisms in plants adapted to phos- phorus (P)-impoverished soils is an important topic in plant physiological ecology (Lambers et al. -
Floristics of the Banksia Woodlands on the Wallingup Plain in Relation to Environmental Parameters
Edith Cowan University Research Online Theses : Honours Theses 2003 Floristics of the banksia woodlands on the Wallingup Plain in relation to environmental parameters Claire McCamish Edith Cowan University Follow this and additional works at: https://ro.ecu.edu.au/theses_hons Part of the Environmental Monitoring Commons Recommended Citation McCamish, C. (2003). Floristics of the banksia woodlands on the Wallingup Plain in relation to environmental parameters. https://ro.ecu.edu.au/theses_hons/359 This Thesis is posted at Research Online. https://ro.ecu.edu.au/theses_hons/359 Edith Cowan University Copyright Warning You may print or download ONE copy of this document for the purpose of your own research or study. The University does not authorize you to copy, communicate or otherwise make available electronically to any other person any copyright material contained on this site. You are reminded of the following: Copyright owners are entitled to take legal action against persons who infringe their copyright. A reproduction of material that is protected by copyright may be a copyright infringement. Where the reproduction of such material is done without attribution of authorship, with false attribution of authorship or the authorship is treated in a derogatory manner, this may be a breach of the author’s moral rights contained in Part IX of the Copyright Act 1968 (Cth). Courts have the power to impose a wide range of civil and criminal sanctions for infringement of copyright, infringement of moral rights and other offences under the Copyright Act 1968 (Cth). Higher penalties may apply, and higher damages may be awarded, for offences and infringements involving the conversion of material into digital or electronic form.