Conservation Advice Eucalyptus Morrisbyi Morrisby's
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A New Leaf-Mining Moth from New Zealand, Sabulopteryx Botanica Sp
A peer-reviewed open-access journal ZooKeys 865: 39–65A new (2019) leaf-mining moth from New Zealand, Sabulopteryx botanica sp. nov. 39 doi: 10.3897/zookeys.865.34265 MONOGRAPH http://zookeys.pensoft.net Launched to accelerate biodiversity research A new leaf-mining moth from New Zealand, Sabulopteryx botanica sp. nov. (Lepidoptera, Gracillariidae, Gracillariinae), feeding on the rare endemic shrub Teucrium parvifolium (Lamiaceae), with a revised checklist of New Zealand Gracillariidae Robert J.B. Hoare1, Brian H. Patrick2, Thomas R. Buckley1,3 1 New Zealand Arthropod Collection (NZAC), Manaaki Whenua–Landcare Research, Private Bag 92170, Auc- kland, New Zealand 2 Wildlands Consultants Ltd, PO Box 9276, Tower Junction, Christchurch 8149, New Ze- aland 3 School of Biological Sciences, The University of Auckland, Private Bag 92019, Auckland, New Zealand Corresponding author: Robert J.B. Hoare ([email protected]) Academic editor: E. van Nieukerken | Received 4 March 2019 | Accepted 3 May 2019 | Published 22 Jul 2019 http://zoobank.org/C1E51F7F-B5DF-4808-9C80-73A10D5746CD Citation: Hoare RJB, Patrick BH, Buckley TR (2019) A new leaf-mining moth from New Zealand, Sabulopteryx botanica sp. nov. (Lepidoptera, Gracillariidae, Gracillariinae), feeding on the rare endemic shrub Teucrium parvifolium (Lamiaceae), with a revised checklist of New Zealand Gracillariidae. ZooKeys 965: 39–65. https://doi.org/10.3897/ zookeys.865.34265 Abstract Sabulopteryx botanica Hoare & Patrick, sp. nov. (Lepidoptera, Gracillariidae, Gracillariinae) is described as a new species from New Zealand. It is regarded as endemic, and represents the first record of its genus from the southern hemisphere. Though diverging in some morphological features from previously de- scribed species, it is placed in genus Sabulopteryx Triberti, based on wing venation, abdominal characters, male and female genitalia and hostplant choice; this placement is supported by phylogenetic analysis based on the COI mitochondrial gene. -
CBD Sixth National Report
Australia’s Sixth National Report to the Convention on Biological Diversity 2014 2018 ‒ 24 March 2020 © Commonwealth of Australia 2020 Ownership of intellectual property rights Unless otherwise noted, copyright (and any other intellectual property rights) in this publication is owned by the Commonwealth of Australia (referred to as the Commonwealth). Creative Commons licence All material in this publication is licensed under a Creative Commons Attribution 4.0 International Licence except content supplied by third parties, logos and the Commonwealth Coat of Arms. Inquiries about the licence and any use of this document should be emailed to [email protected]. Cataloguing data This report should be attributed as: Australia’s Sixth National Report to the Convention on Biological Diversity 2014‒2018, Commonwealth of Australia, Canberra, 2020 CC BY 4.0. ISBN 978-1-76003-255-5 This publication is available at http://www.environment.gov.au/biodiversity/international/un-convention-biological-diversity. Department of Agriculture, Water and the Environment GPO Box 858 Canberra ACT 2601 Telephone 1800 900 090 Web awe.gov.au The Australian Government acting through the Department of Agriculture, Water and the Environment has exercised due care and skill in preparing and compiling the information and data in this publication. Notwithstanding, the Department of Agriculture, Water and the Environment, its employees and advisers disclaim all liability, including liability for negligence and for any loss, damage, injury, expense or cost incurred by any person as a result of accessing, using or relying on any of the information or data in this publication to the maximum extent permitted by law. -
The Taxonomy, Phylogeny and Impact of Mycosphaerella Species on Eucalypts in South-Western Australia
The Taxonomy, Phylogeny and Impact of Mycosphaerella species on Eucalypts in South-Western Australia By Aaron Maxwell BSc (Hons) Murdoch University Thesis submitted in fulfilment of the requirements for the degree of Doctor of Philosophy School of Biological Sciences and Biotechnology Murdoch University Perth, Western Australia April 2004 Declaration I declare that the work in this thesis is of my own research, except where reference is made, and has not previously been submitted for a degree at any institution Aaron Maxwell April 2004 II Acknowledgements This work forms part of a PhD project, which is funded by an Australian Postgraduate Award (Industry) grant. Integrated Tree Cropping Pty is the industry partner involved and their financial and in kind support is gratefully received. I am indebted to my supervisors Associate Professor Bernie Dell and Dr Giles Hardy for their advice and inspiration. Also, Professor Mike Wingfield for his generosity in funding and supporting my research visit to South Africa. Dr Hardy played a great role in getting me started on this road and I cannot thank him enough for opening my eyes to the wonders of mycology and plant pathology. Professor Dell’s great wit has been a welcome addition to his wealth of knowledge. A long list of people, have helped me along the way. I thank Sarah Jackson for reviewing chapters and papers, and for extensive help with lab work and the thinking through of vexing issues. Tania Jackson for lab, field, accommodation and writing expertise. Kar-Chun Tan helped greatly with the RAPD’s research. Chris Dunne and Sarah Collins for writing advice. -
Phenetic Affinities, Variability and Conservation Status of a Rare Tasmanian Endemic, Eucalyptus Morrisbyi R.G
213 PHENETIC AFFINITIES, VARIABILITY AND CONSERVATION STATUS OF A RARE TASMANIAN ENDEMIC, EUCALYPTUS MORRISBYI R.G. BRETT by R.J.E. Wiltshire, B.M. Potts and J.B. Reid (with seven tables and six text-figures) Eucalyptus morrisbyi is a rare Tasmanian endemic confined to one larger population (c. 2000 mature individuals) and two smaller populations (c. 15 and 16 mature individuals) in southeastern Tasmania. Morphological studies within the informal superspecies "Gunnii" reveal Eucalyptus morrisbyi has closest affinities to low altitude populations of E. gunnii in southeastern Tasmania and yet has distinct, phenetic differences from that species. Levels of variation in E. morrisbyi populations appear comparable to other species despite their small population size. A low frequency of hybridisation occurs with E. viminalis in natural stands but is unlikely to have affected the level of variability in the Calverts Hill and Risdon Hill natural populations. In contrast, it is shown that a high frequency of seedlings grown from a planted and a remnant stand of E. morrisbyi have affinities with E. viminalis. Several of the planted trees appeared to be hybrids and some progeny from phenotypically normal trees also appeared to be of hybrid origin. These results suggest that the genetic integrity of the species may be compromised by injudicious selection of seed for propagation from plantings and could be a major problem for the ex situ conservation of this and other rare and endangered species. Recommendations are given to enhance the conservation of this endangered Tasmanian endemic. Key Words: rare endemic, endangered species, conservation, Eucalyptus morrisbyi, Tasmania. In BANKS, M.R. -
Lepidoptera: Geometridae), a Defoliator of Eucalyptus Martin J
Research Collection Journal Article Identification, synthesis and activity of sex pheromonegland components of the autumn gum moth (Lepidoptera:Geometridae), a defoliator of Eucalyptus Author(s): Steinbauer, Martin J.; Östrand, Fredrik; Bellas, Tom E.; Nilson, Anna; Andersson, Fredrik; Hedenström, Erik; Lacey, Michael J.; Schiestl, P. Florian Publication Date: 2004 Permanent Link: https://doi.org/10.3929/ethz-b-000422591 Originally published in: Chemoecology 14(3-4), http://doi.org/10.1007/s00049-004-0281-5 Rights / License: In Copyright - Non-Commercial Use Permitted This page was generated automatically upon download from the ETH Zurich Research Collection. For more information please consult the Terms of use. ETH Library Chemoecology14:217–223 (2004) 0937–7409/04/040217–7 CHEMOECOLOGY © Birkhäuser Verlag, Basel, 2004 DOI 10.1007/s00049-004-0281-5 Identification, synthesis and activity of sex pheromone gland components of the autumn gum moth (Lepidoptera: Geometridae), a defoliator of Eucalyptus Martin J. Steinbauer1, Fredrik Östrand2, Tom E. Bellas3, Anna Nilsson4, Fredrik Andersson4, Erik Hedenström4, Michael J. Lacey3 and Florian P. Schiestl5,6 1Co-operative Research Centre (CRC) for Sustainable Production Forestry and CSIRO Entomology, GPO Box 1700, Canberra, ACT 2601, Australia 2Chemical Ecology and Ecotoxicology, Department of Ecology, Lund University, SE-223 62 Lund, Sweden 3CSIRO Entomology, GPO Box 1700, Canberra, ACT 2601, Australia 4Department of Natural and Environmental Sciences, Mid Sweden University, SE-851 70 Sundsvall, Sweden 5Department of Evolutionary Biology, University of Vienna and School of Botany and Zoology, Australian National University, Canberra, ACT 0200, Australia 6Present address: Geobotanical Institute ETH, 107 Zollikerstrasse, CH-8008 Zürich, Switzerland Summary. The autumn gum moth, Mnesampela privata Introduction (Guenée) (Lepidoptera: Geometridae), is native to Australia and can be a pest of plantation eucalypts. -
Genetic Diversity and Adaptation in Eucalyptus Pauciflora
Genetic diversity and adaptation in Eucalyptus pauciflora Archana Gauli (M.Sc.) A thesis submitted in fulfilment of the requirements for the Degree of Doctor of Philosophy School of Biological Sciences, University of Tasmania June, 2014 Declarations This thesis contains no material which has been accepted for a degree or diploma by the University or any other institution, except by way of background information and duly acknowledged in the thesis, and to the best of the my knowledge and belief no material previously published or written by another person except where due acknowledgement is made in the text of the thesis, nor does the thesis contain any material that infringes copyright. Archana Gauli Date Authority of access This thesis may be made available for loan and limited copying and communication in accordance with the Copyright Act 1968. Archana Gauli Date Statement regarding published work contained in thesis The publishers of the paper comprising Chapter 2 and Chapter 3 hold the copyright for that content, and access to the material should be sought from the respective journals. The remaining non-published content of the thesis may be made available for loan and limited copying and communication in accordance with the Copyright Act 1968. Archana Gauli Date i Statement of publication Chapter 2 has been published as: Gauli A, Vaillancourt RE, Steane DA, Bailey TG, Potts BM (2014) The effect of forest fragmentation and altitude on the mating system of Eucalyptus pauciflora (Myrtaceae). Australian Journal of Botany 61, 622-632. Chapter 3 has been accepted for publication as: Gauli A, Steane DA, Vaillancourt RE, Potts BM (in press) Molecular genetic diversity and population structure in Eucalyptus pauciflora subsp. -
Forest Health News No
forest health news No. 181, February 2008 ISSN 1175-9755 BUDDLEIA LEAF WEEVIL UPDATE indicate weevils become inactive and hide at high temperatures. However, large numbers of very small larvae and eggs were found As reported in an earlier FH News (FH News 169, January 2007) in mid-February at all sites. the buddleia leaf weevil, Cleopus japonicus, was released by Scion staff at five sites in North Island plantations from October 2006 to The weevil can be considered established at all sites as more than January 2007. Release sites were established in Whakarewarewa, two generations have been recorded, weevils were found after Kinleith, Lake Taupo, Esk, and Rawhiti Forests. These forests winter, and numbers have increased. Buddleia leaf weevil feeding were selected because they represent a range of different climatic has been found 145 m from the release plants at Kinleith and conditions. The sites have since been monitored closely for weevil 200 m from them at Lake Taupo. It is only early days, but feeding establishment, dispersal, and feeding damage to buddleia. Despite damage to some plants is impressive. Very heavy defoliation will many years of research in quarantine, how well the weevil would be needed, however, to reduce the vigorous growth of buddleia. do in New Zealand forests was uncertain. Further releases have been made in the Kaikoura area, Whanganui, In particular, we were interested to see if cleopus would survive Masterton, and Bay of Plenty between November 2007 and winter as adult weevils and/or pupae, and would larvae be found February 2008. in the cooler months. -
E.Quadrangulata
Durable Eucalypt Leaflet Series Eucalyptus quadrangulata Ian Nicholas and Paul Millen December 2012 Why grow durable eucalypts? New Zealand’s agricultural landscapes need sustainable land use options adapted to droughts and floods which complement pastoral farming while reducing soil erosion, improving water quality and habitat for native biodiversity. Eucalypts are renowned for their adaptability to droughty and eroding landscapes. They also provide excellent habitat for nectar-feeding birds and insects. With over 400 eucalypt species to select from there is a great opportunity to select appropriate species for the planting objective. With CCA (copper chrome arsenic)-treated wood now banned for many uses by the USA and several European countries, there are significant international and domestic markets for naturally-durable hardwoods. The wood properties of New Zealand grown durable eucalypts ensure they can replace CCA treated material for many uses and are also ideal for a wide range of agricultural and land-based industrial applications, particularly for posts, poles and utility cross-arms as well as heavy structural timbers. NZDFI (New Zealand Dryland Forests Initiative) has selected eucalypt species which can be sawn to produce durable hardwood. Using these species, NZDFI is committed to developing viable best-practice forest management systems to complement livestock farming. NZDFI wants to encourage planting durable hardwood forests and woodlots to protect steeplands and waterways, for shade and shelter, and to generate income from carbon credits and sustainable timber harvesting. Why NZDFI have selected E. quadrangulata? NZDFI have selected species that: • Produce highly durable timber (Class 1 and 2 Australian Standard, AS5606-2005) • Are drought tolerant • Coppice vigorously after fire and harvesting • Do not appear to spread as wildings • Have the potential to sequester carbon faster than pine on drylands • Provide nectar/pollen for native biodiversity. -
01/02 Annual Report (PDF, 6741KB)
M 56 CBC for Sustarnable Production Forestry — Annual Report 2001/02 Publications Genetic Improvement Program McGowen MH, Wiltshire RJ, Potts BM, Vaillancourt RE (2001). The origin of Eucalyptus vernicosa, a Books and book chapters unique shrub eucalypt. Biological Journal of the Auckland LD, Bui T, Zhou Y, Shepherd M, Williams CG Linnean Society 74, 397-405. (2002). Transpecific recovery of pine microsatellite. In ‘Conifer Microsatellite Handbook’. (Eds CG Williams McKinnon GE, Vaillancourt RE, Tilyard PA, Potts BM and LD Auckland) pp. 27-28. (Texas A & M University: (2001). Maternal inheritance of the chloroplast genome College Station, Texas, USA) in Eucalyptus globulus and interspecific hybrids, Genome 44, 831-835. Refereed publications Costa e Silva J, Dutkowski GW, Gilmour AR (2001). Patterson B, Vaillancourt RE, Potts BM (2001). Analysis of early tree height in forest genetic trials is Eucalypt seed collectors: beware of sampling seedlots enhanced by including a spatially correlated residual. from low in the canopy! Australian Forestry 64, 139- Canadian Journal of Forest Research 31, 1887-1893. 142. Dungey HS, Potts BM (2002). Susceptibility of Potts BM, Potts WC, Kantvilas G (2001). The Miena some Eucalyptus species and their hybrids to possum cider gum, Eucalyptus gunnii subsp. (livaricata damage. Australian Forestry 65, 16-23. (Myrtaceae): a taxon in rapid decline. Proceedings of the Royal Society of Tasmania 135, 57-6l. Freeman JS, Jackson HD, Steane DA, McKinnon GE, Dutkowski GW, Potts BM, Vaillancourt RE (2001). Pound LM, Wallwork MAB, Potts BM, Sedgley M _iii_.-_,_ Chloroplast DNA phylogeography of Eucalyptus (2002). Self-incompatibility in Eucalyptus globulus globulus. Australian Journal ofBotany 49, 585-589. -
ARTHROPODA Subphylum Hexapoda Protura, Springtails, Diplura, and Insects
NINE Phylum ARTHROPODA SUBPHYLUM HEXAPODA Protura, springtails, Diplura, and insects ROD P. MACFARLANE, PETER A. MADDISON, IAN G. ANDREW, JOCELYN A. BERRY, PETER M. JOHNS, ROBERT J. B. HOARE, MARIE-CLAUDE LARIVIÈRE, PENELOPE GREENSLADE, ROSA C. HENDERSON, COURTenaY N. SMITHERS, RicarDO L. PALMA, JOHN B. WARD, ROBERT L. C. PILGRIM, DaVID R. TOWNS, IAN McLELLAN, DAVID A. J. TEULON, TERRY R. HITCHINGS, VICTOR F. EASTOP, NICHOLAS A. MARTIN, MURRAY J. FLETCHER, MARLON A. W. STUFKENS, PAMELA J. DALE, Daniel BURCKHARDT, THOMAS R. BUCKLEY, STEVEN A. TREWICK defining feature of the Hexapoda, as the name suggests, is six legs. Also, the body comprises a head, thorax, and abdomen. The number A of abdominal segments varies, however; there are only six in the Collembola (springtails), 9–12 in the Protura, and 10 in the Diplura, whereas in all other hexapods there are strictly 11. Insects are now regarded as comprising only those hexapods with 11 abdominal segments. Whereas crustaceans are the dominant group of arthropods in the sea, hexapods prevail on land, in numbers and biomass. Altogether, the Hexapoda constitutes the most diverse group of animals – the estimated number of described species worldwide is just over 900,000, with the beetles (order Coleoptera) comprising more than a third of these. Today, the Hexapoda is considered to contain four classes – the Insecta, and the Protura, Collembola, and Diplura. The latter three classes were formerly allied with the insect orders Archaeognatha (jumping bristletails) and Thysanura (silverfish) as the insect subclass Apterygota (‘wingless’). The Apterygota is now regarded as an artificial assemblage (Bitsch & Bitsch 2000). -
Genetic Variability and Leaf Waxes of Some Eucalyptus Species with Horticultural Potential
29. *t Genetic Variability and Leaf Waxes of some Eucalyptus Species with Horticultural Potential Michelle Gabrielle Wirthensohn B.Ag.Sc. (Hons) Submitted in fulfîllment of the requirements for the degree of Doctor of Philosophy Department of Horticulture, Viticulture and Oenology Waite Agricultural Research Institute University of Adelaide September 1998 Eucalyptus macrocarpa Anne.ndix Table of Contents Abstract I Declaration iv Acknowledgements v List of Tables vi List of Figures viii Glossary xi Chapter 1 General lntroduction I The genus EucalYPtus 2 Lignotubers and mallee 3 Leaf phases 4 Leaf waxes 5 Wax structure 5 Wax chemistry 5 Ontogenetic variation 8 Wax extraction and seParation t0 Functions of epicuticular wax l0 Glaucousness 10 Environmental adaPtations 11 Influencing factors on epicuticular wax t2 Light t2 Temperature and other environmental effects 12 Etfect of agricultural chemicals on leaf waxes 13 Taxonomic significance of wax structure and composition 13 Thesis aims I4 Chapter 2 Plant Material t6 Species Descriptions and Taxonomy l9 Ghapter 3 Species Evaluation and Pruning lntroduction 25 Materials and Methods Species evaluation 26 Pruning trial on E. globulus 26 Pruning trial on 16 species ol Eucalyptus 27 Pruning trial on E. gunnii 27 Results Species evaluation 28 Pruning trial on E. globulus 28 Pruning trial on 16 species ol Eucalyptus 28 Pruning trial on E. gunnii 30 Discussion 47 Chapter 4 Postharvest Treatment of Gut Stems lntroduction 51 Materials and Methods Plant material 5l Vase life 52 Pulsing 52 Pulsing and -
CHAPTER 5 Molecular Genetic Diversity of E. Urophylla
ABSTRACT PAYN, KITT GARNET. Molecular Genetic Diversity and Population Genetic Structure of the Commercially Important Tropical Forest Tree Species Eucalyptus urophylla. (Under the direction of William S. Dvorak.) Eucalyptus urophylla is an economically important plantation tree species in countries with tropical and subtropical climates. Its natural distribution is limited to a series of populations on seven islands of the Sunda archipelago in eastern Indonesia. The largest populations are found on the islands of Timor and Wetar, whereas smaller populations occur on the islands of Alor, Pantar, Lomblen, Adonara and Flores. Of concern is the depletion in the species’ genetic resource, primarily on the latter five islands, as a consequence of land conversion to agriculture. Proficient management of the E. urophylla genetic resource, with respect to both conservation and breeding programs, requires a good understanding of the level of genetic diversity and population genetic structure across the species’ native range. This may be achieved through the application of DNA marker techniques that measure genetic diversity at different levels (e.g. organellar vs. nuclear, or genome-wide vs. gene locus). Historical events such as range expansion and genetic bottlenecks can leave an imprint on contemporary levels of genetic diversity. Therefore, the geographical distribution of chloroplast DNA sequence variation in E. urophylla was studied to gain insight into its historical seed migration routes along the island archipelago. Chloroplast DNA sequence data were obtained from 198 plants broadly representing the native range of the species. Twenty haplotypes were identified. A moderate to high level of chloroplast genetic differentiation (GST = 0.581, NST = 0.724) and significant phylogeographic structure (NST > GST; P < 0.01) were observed, suggesting low levels of recurrent seed-mediated gene flow among the islands.