Acacia Bartlei 5 Much As They Should Be
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Pollination Ecology, Nectar Secretion Dynamics, and Honey Production
Tropical Ecology 57(3): 429-444, 2016 ISSN 0564-3295 © International Society for Tropical Ecology www.tropecol.com Pollination ecology, nectar secretion dynamics, and honey production potentials of Acacia ehrenbergiana (Hayne) and Acacia tortilis (Forsk.) Hayne, Leguminosae (Mimosoideae), in an arid region of Saudi Arabia NURU ADGABA1*, AL-GHAMDI A. AHMED1, SHENKUTE G. AWRARIS1, MOHAMMED AL-MADANI1, MOHAMMED J. ANSARI1, RACHID SAMMOUDA2 & SARAH E. RADLOFF3 1Chair of Eng. Abdullah Baqshan for Bee Research, Department of Plant Protection, Faculty of Food and Agricultural Science, King Saud University, P.O. Box, 2460, Riyadh 11451KSA 2Department of Computer Science, King Saud University, Riyadh, Saudi Arabia 3 Department of Statistics, Rhodes University, P.O. Box 94, Grahamstown 6140, South Africa Abstract: This study was conducted to investigate the structuring of two sympatric and co- flowering acacia species - Acacia ehrenbergiana (Hayne) and Acacia tortilis (Forsk.) - in relation to their flowering period distribution, floral reward partitioning, nectar secretion dynamics, and visitor assemblages. This research was performed in an arid climatic zone of the Arabian Peninsula (Saudi Arabia). To determine if there is partitioning of pollinators between the two species their peak flowering periods were monitored and the peak time of pollen release through the day was quantified as the ratio of polyads to anthers. The nectar sugar secretion dynamics were estimated following nectar sugar washing techniques. The types and frequency of visitors were recorded and correlated. The two species varied in their peak flowering time within a season and peak pollen release time within a day. Moreover, both species secreted significant amounts of nectar sugar. The sharing of pollinators and the partial monopoly of certain visitors were observed. -
Botanical Name: Acacia Common Name: Wattle Family: Fabaceae Origin: Australia and Africa Habit: Various Habitats Author: Diana Hughes, Mullumbimby
Botanical Name: Acacia Common Name: Wattle Family: Fabaceae Origin: Australia and Africa Habit: various habitats Author: Diana Hughes, Mullumbimby I like to turn to PlantNET-FloraOnline to learn more about plants. Here you will find a wealth of information about plants, their growing habits and distribution. Much can be learnt from Latin names given, plus the variety of common names attributed to each plant. A more familiar name for Acacia is Wattle - Australia's floral emblem, in this case Acacia pycantha, Golden Wattle, which is native to South Eastern Australia. We have beautiful wattles in our region, most of which are coming into flower now. Mullumbimby is famous for the rare Acacia bakeri, (Marblewood), a rainforest species. It is found on the banks of the Brunswick River, with insignificant white flowers, hidden in glossy leaves. Searches through several websites confirm my fears that many Acacias are considered as needing 'environmental management' - meaning they have weed potential. But who could find a field of beautiful Queensland Silver Wattle an unpleasant sight? Negatively they are 'seeders', and positively, they are nitrogen fixers. Managing the four species in my garden is a pleasure. My pride and joy is an Acacia macradenia, or Zig Zag wattle because its phyllodes (leaves) are arranged in that manner along weeping branches. It's about to flower for the 6th year. Motorists stop to photograph it as it is such a sight. I prune it hard each year. My rear raised garden bed holds 3 different species. The well-known Queensland Silver Wattle, or Mt Morgan wattle (Acacia podalyriifolia) is now flowering. -
Acacia Suaveolens
Plants of South Eastern New South Wales Flowering stems and 'leaves'. Australian Plant Image Flower heads, pods, and 'leaves'. Australian Plant Index, photographer Murray Fagg, Australian National Image Index, photographer Murray Fagg, near Forster Botanic Gardens, Canberra, ACT Shrub. Australian Plant Image Index, photographer Line drawing. d. flowering branch showing bracts. M Murray Fagg, Australian National Botanic Gardens, Moir, National Herbarium of Victoria, © 2021 Royal Canberra, ACT Botanic Gardens Board Common name Sweet wattle, Sweet-scented wattle Family Fabaceae Where found Dry forest, woodland, and heath. Coast and ranges. Sightings on the tablelands. Notes Shrub to 3 m tall. Bark smooth. Fleshy seed stalks/arils. Branchlets angled to flattened, hairless, sometimes glaucous. 'Leaves' alternating up the stems, 5-15 cm long, 2-10 mm wide, hairless, more or less glaucous, midvein prominent, margins more or less prominent, tips pointed with a mucro. Flower heads pale yellow to white, globular, 3-10 flowered (easiest seen in late buds), 4-7 mm in diameter, enclosed when young by conspicuous, overlapping bracts, in elongated clusters of 5-12 flower heads. Flowers Autumn to Spring. Family was Mimosaceae. PlantNET description: http://plantnet.rbgsyd.nsw.gov.au/cgi-bin/NSWfl.pl? page=nswfl&lvl=sp&name=Acacia~suaveolens (accessed 28 April 2021) World Wide Wattle photos, line drawings and description: http://www.worldwidewattle.com/imagegallery/image.php? p=0&l=s&id=20591&o=1 Author: Betty Wood. This identification key and fact sheets are available as a free mobile application: Android edition iOS edition Creative Commons Attribution 3.0 Australia (CC BY). -
Human-Mediated Introductions of Australian Acacias
Diversity and Distributions, (Diversity Distrib.) (2011) 17, 771–787 S EDITORIAL Human-mediated introductions of PECIAL ISSUE Australian acacias – a global experiment in biogeography 1 2 1 3,4 David M. Richardson *, Jane Carruthers , Cang Hui , Fiona A. C. Impson , :H Joseph T. Miller5, Mark P. Robertson1,6, Mathieu Rouget7, Johannes J. Le Roux1 and John R. U. Wilson1,8 UMAN 1 Centre for Invasion Biology, Department of ABSTRACT - Botany and Zoology, Stellenbosch University, MEDIATED INTRODUCTIONS OF Aim Australian acacias (1012 recognized species native to Australia, which were Matieland 7602, South Africa, 2Department of History, University of South Africa, PO Box previously grouped in Acacia subgenus Phyllodineae) have been moved extensively 392, Unisa 0003, South Africa, 3Department around the world by humans over the past 250 years. This has created the of Zoology, University of Cape Town, opportunity to explore how evolutionary, ecological, historical and sociological Rondebosch 7701, South Africa, 4Plant factors interact to affect the distribution, usage, invasiveness and perceptions of a Protection Research Institute, Private Bag globally important group of plants. This editorial provides the background for the X5017, Stellenbosch 7599, South Africa, 20 papers in this special issue of Diversity and Distributions that focusses on the 5Centre for Australian National Biodiversity global cross-disciplinary experiment of introduced Australian acacias. A Journal of Conservation Biogeography Research, CSIRO Plant Industry, GPO Box Location Australia and global. 1600, Canberra, ACT, Australia, 6Department of Zoology and Entomology, University of Methods The papers of the special issue are discussed in the context of a unified Pretoria, Pretoria 0002, South Africa, framework for biological invasions. -
Jervis Bay Territory Page 1 of 50 21-Jan-11 Species List for NRM Region (Blank), Jervis Bay Territory
Biodiversity Summary for NRM Regions Species List What is the summary for and where does it come from? This list has been produced by the Department of Sustainability, Environment, Water, Population and Communities (SEWPC) for the Natural Resource Management Spatial Information System. The list was produced using the AustralianAustralian Natural Natural Heritage Heritage Assessment Assessment Tool Tool (ANHAT), which analyses data from a range of plant and animal surveys and collections from across Australia to automatically generate a report for each NRM region. Data sources (Appendix 2) include national and state herbaria, museums, state governments, CSIRO, Birds Australia and a range of surveys conducted by or for DEWHA. For each family of plant and animal covered by ANHAT (Appendix 1), this document gives the number of species in the country and how many of them are found in the region. It also identifies species listed as Vulnerable, Critically Endangered, Endangered or Conservation Dependent under the EPBC Act. A biodiversity summary for this region is also available. For more information please see: www.environment.gov.au/heritage/anhat/index.html Limitations • ANHAT currently contains information on the distribution of over 30,000 Australian taxa. This includes all mammals, birds, reptiles, frogs and fish, 137 families of vascular plants (over 15,000 species) and a range of invertebrate groups. Groups notnot yet yet covered covered in inANHAT ANHAT are notnot included included in in the the list. list. • The data used come from authoritative sources, but they are not perfect. All species names have been confirmed as valid species names, but it is not possible to confirm all species locations. -
Vertebrate Fauna in the Southern Forests of Western Australia
tssN 0085-8129 ODC151:146 VertebrateFauna in The SouthernForests of WesternAustralia A Survey P. CHRISTENSEN,A. ANNELS, G. LIDDELOW AND P. SKINNER FORESTS DEPARTMENT OF WESTERN AUSTRALIA BULLETIN94, 1985 T:- VertebrateFauna in The SouthernForests of WesternAustralia A Survey By P. CHRISTENSEN, A. ANNELS, G. LIDDELOW AND P. SKINNER Edited by Liana ChristensenM.A. (w.A.I.T.) Preparedfor Publicationby Andrew C.A. Cribb B.A. (U.W.A.) P.J. McNamara Acting Conservator of Forcsts 1985 I I r FRONT COVER The Bush R.at (Rattus fuscipes): the most abundantof the native mammals recordedby the surueyteams in WesternAustralia's southernforests. Coverphotograph: B. A. & A. C. WELLS Printed in WesternAustralia Publishedby the ForestsDepartmeDt of WesternAustralia Editor MarianneR.L. Lewis AssistantEditor Andrew C.A. Cribb DesignTrish Ryder CPl9425/7/85- Bf Atthority WILLIAM BENBOW,Aciing Cov€mmenaPrinter, Wesrern Ausrralia + Contents Page SUMMARY SECTION I-INTRODUCTION HistoricalBackground. Recent Perspectives SECTION II-DESCRIPTION OF SURVEY AREA Boundariesand PhysicalFeatures 3 Geology 3 Soils 3 Climate 6 Vegetation 6 VegetationTypes. 8 SECTION III-SURVEY METHODS 13 SECTION IV-SURVEY RESULTSAND LIST OF SPECIES. l6 (A) MAMMALS Discussionof Findings. l6 List of Species (i) IndigenousSpecies .17 (ii) IntroducedSpecies .30 (B) BIRDS Discussionof Findings List of Species .34 (C) REPTILES Discussionof Findings. List of Species. .49 (D) AMPHIBIANS Discussionof Findings. 55 List of Species. 55 (E) FRESHWATER FISH Discussionof Findings. .59 List of Species (i) IndigenousSpecies 59 (ii) IntroducedSpecies 6l SECTION V-GENERALDISCUSSION 63 ACKNOWLEDGEMENTS 68 REFERENCES 69 APPENDICES I-Results from Fauna Surveys 1912-t982 72 II-Results from Other ResearchStudies '74 Within The SurveyArea 1970-1982. -
Acacia Terminalis Subsp
National Recovery Plan Acacia terminalis subsp. terminalis (Sunshine Wattle) Authors: Martin Bremner and Ann Goeth April 2010 © Department of Environment, Climate Change and Water (NSW), 2010 This work is copyright. However, material presented in this plan may be copied for personal use or published for educational purposes, providing that any extracts are fully acknowledged. Apart from this and any other use as permitted under the Copyright Act 1968, no part may be reproduced without prior written permission from the Department of Environment, Climate Change and Water (NSW). Department of Environment, Climate Change and Water (NSW) 59-61 Goulburn Street (PO Box A290) Sydney South NSW 1232 Phone: (02) 9995 5000 (switchboard) Phone: 131 555 (information & publications requests) TTY: (02) 9211 4723 Fax: (02) 9995 5999 Email: [email protected] Website: www.environment.nsw.gov.au Note: This recovery plan sets out the actions necessary to stop the decline of, and support the recovery of, the listed threatened subspecies. The plan has been developed with the involvement and cooperation of a broad range of stakeholders, but individual stakeholders have not necessarily committed to undertaking specific actions. The attainment of objectives and the provision of funds may be subject to budgetary and other constraints affecting the parties involved. Proposed actions may be subject to modification over the life of the plan due to changes in knowledge. Requests for information or comments regarding the recovery program for Acacia terminalis subsp. terminalis are best directed to: The Acacia terminalis subsp. terminalis Recovery Plan Coordinator Biodiversity Conservation Section, Metro Branch Department of Environment, Climate Change and Water (NSW) PO Box 1967 Hurstville NSW 2220 Phone: 02 9585 6678 Cover photo: Martin Bremner This plan should be cited as follows: Department of Environment, Climate Change and Water (NSW) (2010), Recovery Plan for Acacia terminalis terminalis (Sunshine Wattle), Department of Environment, Climate Change and Water (NSW), Sydney. -
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’. -
Post-Fire Recovery of Woody Plants in the New England Tableland Bioregion
Post-fire recovery of woody plants in the New England Tableland Bioregion Peter J. ClarkeA, Kirsten J. E. Knox, Monica L. Campbell and Lachlan M. Copeland Botany, School of Environmental and Rural Sciences, University of New England, Armidale, NSW 2351, AUSTRALIA. ACorresponding author; email: [email protected] Abstract: The resprouting response of plant species to fire is a key life history trait that has profound effects on post-fire population dynamics and community composition. This study documents the post-fire response (resprouting and maturation times) of woody species in six contrasting formations in the New England Tableland Bioregion of eastern Australia. Rainforest had the highest proportion of resprouting woody taxa and rocky outcrops had the lowest. Surprisingly, no significant difference in the median maturation length was found among habitats, but the communities varied in the range of maturation times. Within these communities, seedlings of species killed by fire, mature faster than seedlings of species that resprout. The slowest maturing species were those that have canopy held seed banks and were killed by fire, and these were used as indicator species to examine fire immaturity risk. Finally, we examine whether current fire management immaturity thresholds appear to be appropriate for these communities and find they need to be amended. Cunninghamia (2009) 11(2): 221–239 Introduction Maturation times of new recruits for those plants killed by fire is also a critical biological variable in the context of fire Fire is a pervasive ecological factor that influences the regimes because this time sets the lower limit for fire intervals evolution, distribution and abundance of woody plants that can cause local population decline or extirpation (Keith (Whelan 1995; Bond & van Wilgen 1996; Bradstock et al. -
Adoption, Use and Perception of Australian Acacias Around the World
Diversity and Distributions, (Diversity Distrib.) (2011) 17, 822–836 S BIODIVERSITY Adoption, use and perception of PECIAL ISSUE RESEARCH Australian acacias around the world Christian A. Kull1*, Charlie M. Shackleton2, Peter J. Cunningham3, Catherine Ducatillon4, Jean-Marc Dufour-Dror5, Karen J. Esler6, James B. Friday7, Anto´nio C. Gouveia8, A. R. Griffin9, Elizabete Marchante8, Stephen J. :H Midgley10, Anı´bal Pauchard11, Haripriya Rangan1, David M. Richardson12, Tony Rinaudo13, Jacques Tassin14, Lauren S. Urgenson15, Graham P. von Maltitz16, Rafael D. Zenni17 and Matthew J. Zylstra6 UMAN - MEDIATED INTRODUCTIONS OF 1School of Geography and Environmental Science, ABSTRACT Monash University, Melbourne, Australia, 2Department of Environmental Science, Rhodes Aim To examine the different uses and perceptions of introduced Australian University, Grahamstown, South Africa, 3Sowing acacias (wattles; Acacia subgenus Phyllodineae) by rural households and Seeds of Change in the Sahel Project, SIM, communities. Maradi, Niger Republic, 4INRA, Jardin Thuret, Antibes, France, 5Environmental Policy Center, Location Eighteen landscape-scale case studies around the world, in Vietnam, Jerusalem Institute for Israel Studies, Jerusalem, India, Re´union, Madagascar, South Africa, Congo, Niger, Ethiopia, Israel, France, Israel, 6Department of Conservation Ecology and Portugal, Brazil, Chile, Dominican Republic and Hawai‘i. A Journal of Conservation Biogeography Entomology and Centre for Invasion Biology, Stellenbosch University, South Africa, 7University -
Synoptic Overview of Exotic Acacia, Senegalia and Vachellia (Caesalpinioideae, Mimosoid Clade, Fabaceae) in Egypt
plants Article Synoptic Overview of Exotic Acacia, Senegalia and Vachellia (Caesalpinioideae, Mimosoid Clade, Fabaceae) in Egypt Rania A. Hassan * and Rim S. Hamdy Botany and Microbiology Department, Faculty of Science, Cairo University, Giza 12613, Egypt; [email protected] * Correspondence: [email protected] Abstract: For the first time, an updated checklist of Acacia, Senegalia and Vachellia species in Egypt is provided, focusing on the exotic species. Taking into consideration the retypification of genus Acacia ratified at the Melbourne International Botanical Congress (IBC, 2011), a process of reclassification has taken place worldwide in recent years. The review of Acacia and its segregates in Egypt became necessary in light of the available information cited in classical works during the last century. In Egypt, various taxa formerly placed in Acacia s.l., have been transferred to Acacia s.s., Acaciella, Senegalia, Parasenegalia and Vachellia. The present study is a contribution towards clarifying the nomenclatural status of all recorded species of Acacia and its segregate genera. This study recorded 144 taxa (125 species and 19 infraspecific taxa). Only 14 taxa (four species and 10 infraspecific taxa) are indigenous to Egypt (included now under Senegalia and Vachellia). The other 130 taxa had been introduced to Egypt during the last century. Out of the 130 taxa, 79 taxa have been recorded in literature. The focus of this study is the remaining 51 exotic taxa that have been traced as living species in Egyptian gardens or as herbarium specimens in Egyptian herbaria. The studied exotic taxa are accommodated under Acacia s.s. (24 taxa), Senegalia (14 taxa) and Vachellia (13 taxa). -
Distribution, Ecology and Conservation of the Endangered Shrub, Acacia Meiantha (Fabaceae) in Central West New South Wales
Cunninghamia Date of Publication: September 2020 A journal of plant ecology for eastern Australia ISSN 0727- 9620 (print) • ISSN 2200 - 405X (Online) Distribution, ecology and conservation of the endangered shrub, Acacia meiantha (Fabaceae) in Central West New South Wales Richard W. Medd 593 Cargo Road, Orange NSW 2800, AUSTRALIA. [email protected] Abstract: Acacia meiantha Tindale & Herscovitch, (Fabaceae) a low to medium shrub with root suckering, is only known to occur at three locations, Clarence, Carcalgong and Mullion Creek in Central West New South Wales. These disjunct populations each separated by >60 km, are considered as isolated subpopulations. A compilation of recent field surveys shows that of the 42,000 stem clusters/aggregates of Acacia meiantha estimated across the three geographic locations, the majority, 39,900 (96%) occur in the Mullions Range State Forest subpopulation, where 61% of clusters occur in the remnant native forest areas and 39% in the plantation forestry compartments. At Carcalgong 1,566 stem clusters were recorded along narrow roadside reserves. The Clarence subpopulation consists of < 400 stem clusters precariously situated among a confluence of road, railway and electricity power-line easements. Ecological observations of habitat are presented; information relating to genetic diversity, seed biology, reproductive biology and response to fire is found to be Data Deficient. The threatened species listing as Endangered under both State and Commonwealth legislation is warranted; the species does not occur on any conservation lands, has restricted distribution and abundance, and is vulnerable to ongoing threats. The area (AOO) and extent of occupancy (EOO) are calculated. It occurs at three locations (< 5), has an estimated EOO of 2,900 km2 (< 5,000 km2) and an AOO of 80 km2 (< 500 km2) (IUCN (2019) thresholds in brackets); there are significant threats to the extent and quality of habitats.