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No. 110 MARCH 2002 Price: $5.00
No. 110 MARCH 2002 Price: $5.00 AUSTRALIAN SYSTEMATIC BOTANY SOCIETY INCORPORATED Office Bearers President Vice President Barry Conn W.R.(Bill) Barker Royal Botanic Gardens Sydney Plant Biodiversity Centre Mrs Macquaries Road Hackney Road Sydney NSW 2000 Hackney SA 5069 tel: (02) 9231 8131 tel: (08) 82229303 email: [email protected] email: [email protected] Secretary Treasurer Brendan Lepschi Anthony Whalen Centre for Plant Biodiversity Research Centre for Plant Biodiversity Research Australian National Herbarium Australian National Herbarium GPO Box 1600, Canberra GPO Box 1600, Canberra ACT 2601 ACT 2601 tel: (02) 6246 5167 tel: (02) 6246 5175 email: [email protected] email: [email protected] Councillor Councillor Andrew Rozefelds R.O.(Bob) Makinson Tasmanian Herbarium Royal Botanic Gardens Sydney GPO Box 252-40 Mrs Macquaries Road Hobart, Tasmania 7001 Sydney NSW 2000 tel.: (03) 6226 2635 tel: (02) 9231 8111 email: [email protected] email: [email protected] Public Officer Annette Wilson Australian Biological Resources Study Environment Australia GPO Box 787 CANBERRA ACT 2601 tel: (02) 6250 9417 email: [email protected] Affiliate Society Papua New Guinea Botanical Society ASBS Web site http://www.anbg.gov.au/asbs Publication dates of previous issue Austral.Syst.Bot.Soc.Nsltr 109 (December 2001 issue) Hardcopy: 15th Jan 2002; ASBS Web site: 15th Jan 2002 Australian Systematic Botany Society Newsletter 110 (March 2002) ASBS Inc. Business Council elections with at the Annual General Meeting, which is more than four months after lodgement as A slip for nominations to the next Council is required by the Rules. -
Australia Lacks Stem Succulents but Is It Depauperate in Plants With
Available online at www.sciencedirect.com ScienceDirect Australia lacks stem succulents but is it depauperate in plants with crassulacean acid metabolism (CAM)? 1,2 3 3 Joseph AM Holtum , Lillian P Hancock , Erika J Edwards , 4 5 6 Michael D Crisp , Darren M Crayn , Rowan Sage and 2 Klaus Winter In the flora of Australia, the driest vegetated continent, [1,2,3]. Crassulacean acid metabolism (CAM), a water- crassulacean acid metabolism (CAM), the most water-use use efficient form of photosynthesis typically associated efficient form of photosynthesis, is documented in only 0.6% of with leaf and stem succulence, also appears poorly repre- native species. Most are epiphytes and only seven terrestrial. sented in Australia. If 6% of vascular plants worldwide However, much of Australia is unsurveyed, and carbon isotope exhibit CAM [4], Australia should host 1300 CAM signature, commonly used to assess photosynthetic pathway species [5]. At present CAM has been documented in diversity, does not distinguish between plants with low-levels of only 120 named species (Table 1). Most are epiphytes, a CAM and C3 plants. We provide the first census of CAM for the mere seven are terrestrial. Australian flora and suggest that the real frequency of CAM in the flora is double that currently known, with the number of Ellenberg [2] suggested that rainfall in arid Australia is too terrestrial CAM species probably 10-fold greater. Still unpredictable to support the massive water-storing suc- unresolved is the question why the large stem-succulent life — culent life-form found amongst cacti, agaves and form is absent from the native Australian flora even though euphorbs. -
Cairns Regional Council Water and Waste Report for Mulgrave River Aquifer Feasibility Study Flora and Fauna Report
Cairns Regional Council Water and Waste Report for Mulgrave River Aquifer Feasibility Study Flora and Fauna Report November 2009 Contents 1. Introduction 1 1.1 Background 1 1.2 Scope 1 1.3 Project Study Area 2 2. Methodology 4 2.1 Background and Approach 4 2.2 Demarcation of the Aquifer Study Area 4 2.3 Field Investigation of Proposed Bore Hole Sites 5 2.4 Overview of Ecological Values Descriptions 5 2.5 PER Guidelines 5 2.6 Desktop and Database Assessments 7 3. Database Searches and Survey Results 11 3.1 Information Sources 11 3.2 Species of National Environmental Significance 11 3.3 Queensland Species of Conservation Significance 18 3.4 Pest Species 22 3.5 Vegetation Communities 24 3.6 Regional Ecosystem Types and Integrity 28 3.7 Aquatic Values 31 3.8 World Heritage Values 53 3.9 Results of Field Investigation of Proposed Bore Hole Sites 54 4. References 61 Table Index Table 1: Summary of NES Matters Protected under Part 3 of the EPBC Act 5 Table 2 Summary of World Heritage Values within/adjacent Aquifer Area of Influence 6 Table 3: Species of NES Identified as Occurring within the Study Area 11 Table 4: Summary of Regional Ecosystems and Groundwater Dependencies 26 42/15610/100421 Mulgrave River Aquifer Feasibility Study Flora and Fauna Report Table 5: Freshwater Fish Species in the Mulgrave River 36 Table 6: Estuarine Fish Species in the Mulgrave River 50 Table 7: Description of potential borehole field in Aloomba as of 20th August, 2009. 55 Figure Index Figure 1: Regional Ecosystem Conservation Status and Protected Species Observation 21 Figure 2: Vegetation Communities and Groundwater Dependencies 30 Figure 3: Locations of Study Sites 54 Appendices A Database Searches 42/15610/100421 Mulgrave River Aquifer Feasibility Study Flora and Fauna Report 1. -
Native Plants Sixth Edition Sixth Edition AUSTRALIAN Native Plants Cultivation, Use in Landscaping and Propagation
AUSTRALIAN NATIVE PLANTS SIXTH EDITION SIXTH EDITION AUSTRALIAN NATIVE PLANTS Cultivation, Use in Landscaping and Propagation John W. Wrigley Murray Fagg Sixth Edition published in Australia in 2013 by ACKNOWLEDGEMENTS Reed New Holland an imprint of New Holland Publishers (Australia) Pty Ltd Sydney • Auckland • London • Cape Town Many people have helped us since 1977 when we began writing the first edition of Garfield House 86–88 Edgware Road London W2 2EA United Kingdom Australian Native Plants. Some of these folk have regrettably passed on, others have moved 1/66 Gibbes Street Chatswood NSW 2067 Australia to different areas. We endeavour here to acknowledge their assistance, without which the 218 Lake Road Northcote Auckland New Zealand Wembley Square First Floor Solan Road Gardens Cape Town 8001 South Africa various editions of this book would not have been as useful to so many gardeners and lovers of Australian plants. www.newhollandpublishers.com To the following people, our sincere thanks: Steve Adams, Ralph Bailey, Natalie Barnett, www.newholland.com.au Tony Bean, Lloyd Bird, John Birks, Mr and Mrs Blacklock, Don Blaxell, Jim Bourner, John Copyright © 2013 in text: John Wrigley Briggs, Colin Broadfoot, Dot Brown, the late George Brown, Ray Brown, Leslie Conway, Copyright © 2013 in map: Ian Faulkner Copyright © 2013 in photographs and illustrations: Murray Fagg Russell and Sharon Costin, Kirsten Cowley, Lyn Craven (Petraeomyrtus punicea photograph) Copyright © 2013 New Holland Publishers (Australia) Pty Ltd Richard Cummings, Bert -
Temperate and Tropical Podocarps: How Ecologically Alike Are They? David A
7 Temperate and Tropical Podocarps: How Ecologically Alike Are They? David A. Coomes and Peter J. Bellingham ABSTRACT. With few exceptions, podocarps are specialists of nutrient-poor soils within temperate and tropical rainforests. They are locally abundant in some tropical mountains, especially near the tree line, and in the lowland tropics most are confined to heathlands and impoverished habitats, although some can persist in forest understories. The ecology of tropical podocarps is not well understood, so here we draw on literature from temperate regions to help characterize their niches. Temperate podocarps are ef- fective at capturing and retaining nutrients at the expense of competitors. They are uni- versally slow growing, but this is not necessarily an encumbrance on poor soils because competition for light is relatively weak. Temperate podocarps are often outcompeted on richer soils because several factors stack against them: they are ill equipped to compete with angiosperms in the race to occupy canopy gaps, there may be few sites for their establishment on the forest floors, and continuous regeneration by podocarps is seldom found in the forest understory because their growth is severely hampered by shading. We suggest that competition excludes imbricate- leaved podocarps from most lowland tropi- cal forests, whereas broad- leaved species with anastomosing veins (Nageia and some Podocarpus) are so shade tolerant that they regenerate beneath closed canopies. INTRODUCTION In 1989, Bond revisited an old but unresolved question: why were coni- David A. Coomes, Forest Conservation and fers pushed out of the lowland tropics and mesic temperate regions by angio- Ecology Group, Department of Plant Sciences, sperms as they diversified and expanded in range during the Late Cretaceous? University of Cambridge, Cambridge CB2 3EA, UK. -
Rates of Molecular Evolution and Diversification in Plants: Chloroplast
Duchene and Bromham BMC Evolutionary Biology 2013, 13:65 http://www.biomedcentral.com/1471-2148/13/65 RESEARCH ARTICLE Open Access Rates of molecular evolution and diversification in plants: chloroplast substitution rates correlate with species-richness in the Proteaceae David Duchene* and Lindell Bromham Abstract Background: Many factors have been identified as correlates of the rate of molecular evolution, such as body size and generation length. Analysis of many molecular phylogenies has also revealed correlations between substitution rates and clade size, suggesting a link between rates of molecular evolution and the process of diversification. However, it is not known whether this relationship applies to all lineages and all sequences. Here, in order to investigate how widespread this phenomenon is, we investigate patterns of substitution in chloroplast genomes of the diverse angiosperm family Proteaceae. We used DNA sequences from six chloroplast genes (6278bp alignment with 62 taxa) to test for a correlation between diversification and the rate of substitutions. Results: Using phylogenetically-independent sister pairs, we show that species-rich lineages of Proteaceae tend to have significantly higher chloroplast substitution rates, for both synonymous and non-synonymous substitutions. Conclusions: We show that the rate of molecular evolution in chloroplast genomes is correlated with net diversification rates in this large plant family. We discuss the possible causes of this relationship, including molecular evolution driving diversification, speciation increasing the rate of substitutions, or a third factor causing an indirect link between molecular and diversification rates. The link between the synonymous substitution rate and clade size is consistent with a role for the mutation rate of chloroplasts driving the speed of reproductive isolation. -
Jones Cross 2006 Index
AN INDEX AND ORCHID SPECIES CROSS REFERENCE TO JONES, D.L. (2006) A Complete Guide to Native Orchids of Australia including the Island Territories Compiled by David Gillingham - A.N.O.S. (Qld) Kabi Group Inc. Contents: Page 1: Contents Explanations/Introduction References General Comments Page 2: The Jones "Dendrobium Alliance" - Comments, Notes, Cross Index Page 3: The Jones "Bulbophyllum Alliance" - Cross Index Page 4: The Jones "Vanda Alliance" - Notes, Cross Index Page 5: The Jones "Miscellaneous Epiphytes" - Notes, Cross Index Page 6: The Dendrobium speciosum/Thelychiton speciosus Complex Explanations/Introduction: There can be little doubt that David Jones's (2006) book A Complete Guide to Native Orchids of Australia including the Island Territories provides probably the most current and most comprehensive coverage of Australia's native orchids available between one set of covers. However whether, and to what extent, the very substantial taxonomic restructure presented in the book is accepted by the professional botanical community, only time will tell. In the meantime, while many orchid growers will enthusiastically embrace these new taxonomies, many others will exercise their valid right to continue labelling their orchids using the older taxa, waiting for the dust to settle on the scientific debate. In either regard there are difficulties for users of Jones's book, in their attempt to relate many of these new taxa to older species descriptors. The individual species entries in the text provide no prior taxonomic information whatever; and the index is of limited assistance, and far from complete regarding taxonomic descriptors commonly used over the past decade or so. -
WHO Country Cooperation Strategy for the Commonwealth of the Northern Mariana Islands 2013-2017
WHO Country Cooperation Strategy for the Commonwealth of the Northern Mariana Islands 2013-2017 WHO Country Cooperation Strategy for the Commonwealth of the Northern Mariana Islands 2013-2017 © World Health Organization 2012 All rights reserved. Publications of the World Health Organization can be obtained from WHO Press, World Health Organization, 20 Avenue Appia, 1211 Geneva 27, Switzerland (tel.: +41 22 791 3264; fax: +41 22 791 4857; e-mail: [email protected]). Requests for permission to reproduce or translate WHO publications – whether for sale or for noncommercial distribution – should be addressed to WHO Press, at the above address (fax: +41 22 791 4806; e-mail: [email protected]). For WHO Western Pacific Regional Publications, request for permission to reproduce should be addressed to the Publications Office, World Health Organization, Regional Office for the Western Pacific, P.O. Box 2932, 1000, Manila, Philippines, (fax: +632 521 1036, e-mail: [email protected]). The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the World Health Organization concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. Dotted lines on maps represent approximate border lines for which there may not yet be full agreement. The mention of specific companies or of certain manufacturers’ products does not imply that they are endorsed or recommended by the World Health Organization in preference to others of a similar nature that are not mentioned. Errors and omissions excepted, the names of proprietary products are distinguished by initial capital letters. -
(OUV) of the Wet Tropics of Queensland World Heritage Area
Handout 2 Natural Heritage Criteria and the Attributes of Outstanding Universal Value (OUV) of the Wet Tropics of Queensland World Heritage Area The notes that follow were derived by deconstructing the original 1988 nomination document to identify the specific themes and attributes which have been recognised as contributing to the Outstanding Universal Value of the Wet Tropics. The notes also provide brief statements of justification for the specific examples provided in the nomination documentation. Steve Goosem, December 2012 Natural Heritage Criteria: (1) Outstanding examples representing the major stages in the earth’s evolutionary history Values: refers to the surviving taxa that are representative of eight ‘stages’ in the evolutionary history of the earth. Relict species and lineages are the elements of this World Heritage value. Attribute of OUV (a) The Age of the Pteridophytes Significance One of the most significant evolutionary events on this planet was the adaptation in the Palaeozoic Era of plants to life on the land. The earliest known (plant) forms were from the Silurian Period more than 400 million years ago. These were spore-producing plants which reached their greatest development 100 million years later during the Carboniferous Period. This stage of the earth’s evolutionary history, involving the proliferation of club mosses (lycopods) and ferns is commonly described as the Age of the Pteridophytes. The range of primitive relict genera representative of the major and most ancient evolutionary groups of pteridophytes occurring in the Wet Tropics is equalled only in the more extensive New Guinea rainforests that were once continuous with those of the listed area. -
Epilist 1.0: a Global Checklist of Vascular Epiphytes
Zurich Open Repository and Archive University of Zurich Main Library Strickhofstrasse 39 CH-8057 Zurich www.zora.uzh.ch Year: 2021 EpiList 1.0: a global checklist of vascular epiphytes Zotz, Gerhard ; Weigelt, Patrick ; Kessler, Michael ; Kreft, Holger ; Taylor, Amanda Abstract: Epiphytes make up roughly 10% of all vascular plant species globally and play important functional roles, especially in tropical forests. However, to date, there is no comprehensive list of vas- cular epiphyte species. Here, we present EpiList 1.0, the first global list of vascular epiphytes based on standardized definitions and taxonomy. We include obligate epiphytes, facultative epiphytes, and hemiepiphytes, as the latter share the vulnerable epiphytic stage as juveniles. Based on 978 references, the checklist includes >31,000 species of 79 plant families. Species names were standardized against World Flora Online for seed plants and against the World Ferns database for lycophytes and ferns. In cases of species missing from these databases, we used other databases (mostly World Checklist of Selected Plant Families). For all species, author names and IDs for World Flora Online entries are provided to facilitate the alignment with other plant databases, and to avoid ambiguities. EpiList 1.0 will be a rich source for synthetic studies in ecology, biogeography, and evolutionary biology as it offers, for the first time, a species‐level overview over all currently known vascular epiphytes. At the same time, the list represents work in progress: species descriptions of epiphytic taxa are ongoing and published life form information in floristic inventories and trait and distribution databases is often incomplete and sometimes evenwrong. -
Rates of Molecular Evolution and Diversification in Plants: Chloroplast
Duchene and Bromham BMC Evolutionary Biology 2013, 13:65 http://www.biomedcentral.com/1471-2148/13/65 RESEARCH ARTICLE Open Access Rates of molecular evolution and diversification in plants: chloroplast substitution rates correlate with species-richness in the Proteaceae David Duchene* and Lindell Bromham Abstract Background: Many factors have been identified as correlates of the rate of molecular evolution, such as body size and generation length. Analysis of many molecular phylogenies has also revealed correlations between substitution rates and clade size, suggesting a link between rates of molecular evolution and the process of diversification. However, it is not known whether this relationship applies to all lineages and all sequences. Here, in order to investigate how widespread this phenomenon is, we investigate patterns of substitution in chloroplast genomes of the diverse angiosperm family Proteaceae. We used DNA sequences from six chloroplast genes (6278bp alignment with 62 taxa) to test for a correlation between diversification and the rate of substitutions. Results: Using phylogenetically-independent sister pairs, we show that species-rich lineages of Proteaceae tend to have significantly higher chloroplast substitution rates, for both synonymous and non-synonymous substitutions. Conclusions: We show that the rate of molecular evolution in chloroplast genomes is correlated with net diversification rates in this large plant family. We discuss the possible causes of this relationship, including molecular evolution driving diversification, speciation increasing the rate of substitutions, or a third factor causing an indirect link between molecular and diversification rates. The link between the synonymous substitution rate and clade size is consistent with a role for the mutation rate of chloroplasts driving the speed of reproductive isolation. -
Associations of Societies for Growing Australian Plants
Page 1 Associations of Societies for Growing Australian Plants – Rainforest Study Group – No.62 (7) June 2006 Associations of Societies for Growing Australian Plants ASGAP Rainforest Study Group NEWSLETTER No 62. (7) June 2006 ISSN 0729-5413 Annual Subscription $5, $10 overseas Photos: www.web-a-file.com Study Group Webpage (under construction): http://farrer.csu.edu.au/ASGAP/rainfor.html Email: [email protected] Address: Kris Kupsch, 28 Plumtree Pocket, Burringbar, Australia, 2483. Ph. (02) 66771466 Mob. 0439557438 Introduction ASGAP trip to Sydney Nov 2005 It has been a long while since I wrote a During my brief visit to Sydney in November newsletter, I apologise for taking so long. last year as part of an invitation to speak at a Since the last newsletter the family and I have SGAP meeting in Ermington, I got to do the moved back to the Wet Tropics. I now work following: as an Environmental Scientist undertaking 1. I was escorted by Cas Liber, ASGAP vegetation surveys and compiling Banksia Study Group leader. Cas environmental management plans for parts of toured me through the Botanic the Wet Tropics World Heritage Area. This Gardens, his garden, among others. has been a rather large transition, leaving Many thanks to Cas and his family. behind my garden and all of my immediate 2. I visited Betty Rymers garden at plans in NSW; the job was too good to refuse. Kenthurst. Betty has a notable I wish everyone the best with their rainforest garden including a large endeavours and hope this newsletter was Brachychiton discolor, Dianella worth the wait.