The Victorian Naturalist
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Cravens Peak Scientific Study Report
Geography Monograph Series No. 13 Cravens Peak Scientific Study Report The Royal Geographical Society of Queensland Inc. Brisbane, 2009 The Royal Geographical Society of Queensland Inc. is a non-profit organization that promotes the study of Geography within educational, scientific, professional, commercial and broader general communities. Since its establishment in 1885, the Society has taken the lead in geo- graphical education, exploration and research in Queensland. Published by: The Royal Geographical Society of Queensland Inc. 237 Milton Road, Milton QLD 4064, Australia Phone: (07) 3368 2066; Fax: (07) 33671011 Email: [email protected] Website: www.rgsq.org.au ISBN 978 0 949286 16 8 ISSN 1037 7158 © 2009 Desktop Publishing: Kevin Long, Page People Pty Ltd (www.pagepeople.com.au) Printing: Snap Printing Milton (www.milton.snapprinting.com.au) Cover: Pemberton Design (www.pembertondesign.com.au) Cover photo: Cravens Peak. Photographer: Nick Rains 2007 State map and Topographic Map provided by: Richard MacNeill, Spatial Information Coordinator, Bush Heritage Australia (www.bushheritage.org.au) Other Titles in the Geography Monograph Series: No 1. Technology Education and Geography in Australia Higher Education No 2. Geography in Society: a Case for Geography in Australian Society No 3. Cape York Peninsula Scientific Study Report No 4. Musselbrook Reserve Scientific Study Report No 5. A Continent for a Nation; and, Dividing Societies No 6. Herald Cays Scientific Study Report No 7. Braving the Bull of Heaven; and, Societal Benefits from Seasonal Climate Forecasting No 8. Antarctica: a Conducted Tour from Ancient to Modern; and, Undara: the Longest Known Young Lava Flow No 9. White Mountains Scientific Study Report No 10. -
Entomology of the Aucklands and Other Islands South of New Zealand: Lepidoptera, Ex Cluding Non-Crambine Pyralidae
Pacific Insects Monograph 27: 55-172 10 November 1971 ENTOMOLOGY OF THE AUCKLANDS AND OTHER ISLANDS SOUTH OF NEW ZEALAND: LEPIDOPTERA, EX CLUDING NON-CRAMBINE PYRALIDAE By J. S. Dugdale1 CONTENTS Introduction 55 Acknowledgements 58 Faunal Composition and Relationships 58 Faunal List 59 Key to Families 68 1. Arctiidae 71 2. Carposinidae 73 Coleophoridae 76 Cosmopterygidae 77 3. Crambinae (pt Pyralidae) 77 4. Elachistidae 79 5. Geometridae 89 Hyponomeutidae 115 6. Nepticulidae 115 7. Noctuidae 117 8. Oecophoridae 131 9. Psychidae 137 10. Pterophoridae 145 11. Tineidae... 148 12. Tortricidae 156 References 169 Note 172 Abstract: This paper deals with all Lepidoptera, excluding the non-crambine Pyralidae, of Auckland, Campbell, Antipodes and Snares Is. The native resident fauna of these islands consists of 42 species of which 21 (50%) are endemic, in 27 genera, of which 3 (11%) are endemic, in 12 families. The endemic fauna is characterised by brachyptery (66%), body size under 10 mm (72%) and concealed, or strictly ground- dwelling larval life. All species can be related to mainland forms; there is a distinctive pre-Pleistocene element as well as some instances of possible Pleistocene introductions, as suggested by the presence of pairs of species, one member of which is endemic but fully winged. A graph and tables are given showing the composition of the fauna, its distribution, habits, and presumed derivations. Host plants or host niches are discussed. An additional 7 species are considered to be non-resident waifs. The taxonomic part includes keys to families (applicable only to the subantarctic fauna), and to genera and species. -
PROTEACEAE – It's All About Pollination
PROTEACEAE – it’s all about pollination …….Gail Slykhuis Illustration Philippa Hesterman, images Ellinor Campbell & Marg McDonald A predominantly southern hemisphere plant family, Proteaceae is well represented in Australia, particularly in the West, but we do have our own equally special local representatives, some of which are outlined below. A characteristic feature of many genera within this plant family is the ‘pollen presenter’, which is a fascinating mechanism by which the pollen, which would otherwise be difficult to access for potential pollination vectors such as bees, birds and nectarivorous mammals, is positioned on the extended style of the flower, facilitating cross- pollination. The stigma, which is part of the style, is not mature at this time, thus avoiding self-pollination. A hand lens would enable you to clearly see pollen presenters on the following local representatives: Banksia marginata, Grevillea infecunda, Hakea spp., Isopogon ceratophyllus and Lomatia illicifolia. It is interesting to note that both Victorian Smoke-bush Conospermum mitchellii and Prickly Geebung Persoonia juniperina, also found in our district, do not have pollen presenters. Silver Banksia Banksia marginata This shrub or small tree is readily recognisable when flowering (Feb – July) by the conspicuous yellow pollen presenters, which are an obvious floral part of the banksia flower. These flowers then slowly mature into our iconic woody banksia cones. It is interesting to observe the changes in the nature of the pollen presenters as the flower develops. The white undersides of the leathery leaves provide a clue to the choice of common name with their tip being characteristically blunt or truncate. Anglesea Grevillea Grevillea infecunda One of our endemic plants, the Anglesea Grevillea was first named in 1986 and is Anglesea Grevillea found in several locations north west of Anglesea. -
Rodondo Island
BIODIVERSITY & OIL SPILL RESPONSE SURVEY January 2015 NATURE CONSERVATION REPORT SERIES 15/04 RODONDO ISLAND BASS STRAIT NATURAL AND CULTURAL HERITAGE DIVISION DEPARTMENT OF PRIMARY INDUSTRIES, PARKS, WATER AND ENVIRONMENT RODONDO ISLAND – Oil Spill & Biodiversity Survey, January 2015 RODONDO ISLAND BASS STRAIT Biodiversity & Oil Spill Response Survey, January 2015 NATURE CONSERVATION REPORT SERIES 15/04 Natural and Cultural Heritage Division, DPIPWE, Tasmania. © Department of Primary Industries, Parks, Water and Environment ISBN: 978-1-74380-006-5 (Electronic publication only) ISSN: 1838-7403 Cite as: Carlyon, K., Visoiu, M., Hawkins, C., Richards, K. and Alderman, R. (2015) Rodondo Island, Bass Strait: Biodiversity & Oil Spill Response Survey, January 2015. Natural and Cultural Heritage Division, DPIPWE, Hobart. Nature Conservation Report Series 15/04. Main cover photo: Micah Visoiu Inside cover: Clare Hawkins Unless otherwise credited, the copyright of all images remains with the Department of Primary Industries, Parks, Water and Environment. This work is copyright. It may be reproduced for study, research or training purposes subject to an acknowledgement of the source and no commercial use or sale. Requests and enquiries concerning reproduction and rights should be addressed to the Branch Manager, Wildlife Management Branch, DPIPWE. Page | 2 RODONDO ISLAND – Oil Spill & Biodiversity Survey, January 2015 SUMMARY Rodondo Island was surveyed in January 2015 by staff from the Natural and Cultural Heritage Division of the Department of Primary Industries, Parks, Water and Environment (DPIPWE) to evaluate potential response and mitigation options should an oil spill occur in the region that had the potential to impact on the island’s natural values. Spatial information relevant to species that may be vulnerable in the event of an oil spill in the area has been added to the Australian Maritime Safety Authority’s Oil Spill Response Atlas and all species records added to the DPIPWE Natural Values Atlas. -
Archiv Für Naturgeschichte
© Biodiversity Heritage Library, http://www.biodiversitylibrary.org/; www.zobodat.at Bericht über die wissenschaftlichen Leistungen im Gebiete der Arthropoden während des Jahres 1883. Von Dr. Ph. Bertkaa in Bonn. Eingsley scheint geneigt zu sein, die von ihm aufgeworfene Frage: Is the group Arthropoda a valid one? zu ver- neinen, indem er auf die verschiedene Zahl der Fühler, Mundtheile, die verschiedene Entwickehmg, Beschaffenheit derVerdauungs- und Respirations- und Circulationsorgane der Crustaceen und Insekten hinweist; die Tardigraden, Pycnogoniden , Linguatulinen und Limulus sind vielleicht als Gruppen aequivalent den Insekten und Crustaceen, vielleicht auch als Zweige des Arachniden- stammes anzusehen; jedenfalls gehören sie nicht zum Phylum der Crustaceen; Americ. Naturalist 1883 S. 1034 ff. Packard in seinem Aufsatze: On the Morphology of the Myriapoda führt bei der Benennung der Kopftheile und ihrer Anhänge einige neue Bezeichnungen ein. Auf Grund der Embryonalentwicklung sieht er die Chilognatha als die ursprüng- lichere Ordnung an, die von einem „Leptus-ähnlichen" Vorfahr, d. h. einem Tracheaten, wie es der aus dem Ei schlüpfende junge Chilognath ist, mit 3 Paar Kopfgliedmassen und 3 Bein- paaren, abstammen. Diesem Vorfahr kommen Eurypauropus und Pauropus am nächsten, die nicht als eine besondere Ordnung, sondern als eine zweite Unterordnung der Chilognathen neben den Ch. genuina anzusehen sind, und zwar vermittelt Eurypauropus den üebergang zu Polyxenus. — Scolopendrella ist kein Myria- pode, sondern ein Thysanure. — Palaeocampa, die Scudder zu einem Chilognathen gemacht hatte, ist wahrscheinlich eine haarige Neuropterenlarve. Arcli. f. Natuigesch. L. Jahrg. 2. Bd. A 2 Bertkau: Bericht über die wissenschaftlichen © Biodiversity Heritage Library, http://www.biodiversitylibrary.org/; www.zobodat.at Die Myriapoden mit ihren sechsbeinigen Jugendstadien haben keinen gemeinsamen näheren Ursprung mit den Insekten und Arachniden, bei denen gerade in der Embryonalentwickelung vielfach Boiupaare auftreten, die hernach verschwinden. -
Muelleria : an Australian Journal of Botany
Muelleria Volume 5 Number 1 March, 1982 NATIONAL HERBARIUM OF VICTORIA DEPARTMENT OF CROWN LANDS AND SURVEY Muelleria Volume 5, Number 1 March, 1982 CONTENTS Page A revision of the genus Templelonia R.Br. (Papilionaceae) — J. H. Ross 1 The nomenclature of some Australian lichens described as Lecanora and Placodium by Miiller-Argoviensis — R. W. Rogers 31 New Australian species of Nymphoides Seguier (Menyanthaceae) — Helen 1. Aston 35 Vegetation of East Gippsland — S. J. Forbes, N. G. Walsh and P. K. Gullan 53 A new Australian lichen: Cladonia sulcata — A. W. Archer 115 Editor: Helen 1. Aston Published by the National Herbarium of Victoria (MEL). Royal Botanic Gardens, South Yarra, Victoria 3141, Australia. D. M. Churchill, Director and Government Botanist. 43346/81 The date of publication of Volume 4, number 4, was 20 May 1981. A REVISION OF THE GENUS TEMPLETONIA R.Br. (PAPILIONACEAE) by J. H. Ross* ABSTRACT The endemic Australian genus Templetonia is revised. Eleven species are recognized and the uncertainty concerning the application of the name T. sulcata (Meissn.) Benth. is discussed. This discussion includes the selection ol a lectotype for Bossiaea rossii F. Muell., a possible synonym. Descriptions, a key to the identification of species, illustrations, and distribution maps are provided, together with notes on ecology and relationships. Two previous papers describing T. incana (.Muelleria 4: 247-249 (1980)) and T. negketa (loc. cit. 390-393 (1981)) should be used in conjunction with the present revision. INTRODUCTION Templetonia, a small genus of 1 1 species described by R. Brown in Ait. f Hort. , Kew. ed. 2, 4: 269 (1812), was named in honour of the Irish botanist John Templeton (1776-1825) ot Orange Grove, Belfast. -
Pollination Ecology and Evolution of Epacrids
Pollination Ecology and Evolution of Epacrids by Karen A. Johnson BSc (Hons) Submitted in fulfilment of the requirements for the Degree of Doctor of Philosophy University of Tasmania February 2012 ii Declaration of originality This thesis contains no material which has been accepted for the award of any other 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 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. Karen A. Johnson Statement of authority of access This thesis may be made available for copying. Copying of any part of this thesis is prohibited for two years from the date this statement was signed; after that time limited copying is permitted in accordance with the Copyright Act 1968. Karen A. Johnson iii iv Abstract Relationships between plants and their pollinators are thought to have played a major role in the morphological diversification of angiosperms. The epacrids (subfamily Styphelioideae) comprise more than 550 species of woody plants ranging from small prostrate shrubs to temperate rainforest emergents. Their range extends from SE Asia through Oceania to Tierra del Fuego with their highest diversity in Australia. The overall aim of the thesis is to determine the relationships between epacrid floral features and potential pollinators, and assess the evolutionary status of any pollination syndromes. The main hypotheses were that flower characteristics relate to pollinators in predictable ways; and that there is convergent evolution in the development of pollination syndromes. -
Epacris Study Group
ASSOCIATION OF SOCIETIES FOR GROWING AUSTRALIAN PLANTS Inc. EPACRIS STUDY GROUP Group Leader: Gwen Elliot, P.O. Box 655 Heathmont Vic. 3135 NEWSLETTER No. XS (ISSN 103 8-6017) Qctaber zaQ4 Greetings as once again we begin to enjoy the longer days of spring-summer and the encouragement this provides for many of our flowering plants. Despite the generally dry conditions many Epacris species are putting on outstanding floral displays. How are you going with your recording of the flowering times of Epacris impressa in your garden, as well as in nearby bushland or in other areas as you travel within Australia? It really is quite an exciting project because together we, as Study Group members, can make a real contribution to the overall understanding of this species, adding to the knowledge and research of botanists who look in detail at the features of the plant under the microscope and in its natural habitat. It iis a species which occurs both atsea-level and at higher altitudes. How are the flowering times affected when highland plants are cultivated at lower altitudes? Are flowering times different when plants fiom New South Wales for example are gvown much further south in soulhern Victoria or Tasmania ? Epacris impressu seems like an excellent species for us to research in this way. If our project is successful we may perhaps be able to continue with looking at the flowering times of other Epacris which are relatively common in cultivation. In case you have misplaced the recording sheet from our October 2003 Newsletter, another is included in this issue. -
Kamilaroi and Kurnai : Group-Marriage and Relationship
^^!fvolume handle t^*^° BOOK 572.9g4.F54 c. 1 FISON # KAMILAROI AND KURNAI 3 T1S3 0013flTflb 7 |K, 64 2-^ KAMILAKOI AND KUENAI MANEROO TABLE LAND. BASS'S STRAITS KAIILAROI AID KFRIAI GROUP-MARRIAGE AND RELATIONSHIP, AND MARRIAGE BY ELOPEMENT Drawn chiefly from the usage of the Australian Aborigines THE KURNAI TRIBE Their customs in Peace and War BY LORIMER FISON, M.A., and A. W. HOWITT, F.G.S. WITH AN INTRODUCTION BY LEWIS H. MORGAN, LL.D. AUTHOR OP ''Systems of Consanguinity," "Ancient Society," &c. ' Imlkiis monstrare recentihus ahilita rpriim."—HOR. GEORGE ROBERTSON MELBOURNE, SYDNEY, ADELAIDE, AND BRISBANE MDCCCLXXX [All rights reserved.] TO THE HONOURABLE LEWIS H. MORGAN, LL.D., THIS VOLUME ©eUicatetr, AS A TOKEN OF ESTEEM, B Y THE A UTHORS. CONTENTS. PREFATORY NOTE ... ... 1 KAMILAROI MARRIAGE, DESCENT, AND RELATIONSHIP 21 GROUP MARRIAGE AND RELATIONSHIP 97 THE KURNAI, THEIR CUSTOMS IN PEACE AND WAR ... 177 THEORY OF THE KURNAI SYSTEM 293 SUMMARY AND GENERAL CONCLUSIONS 315 — — ERRATA. P. 4-}. The following statcmeut, which occurs here, requires correction : "The two sets of gentes are conterminous with the original classes; and, descent being through the mother, they alternate between those classes in alternate generations. Ipai-Kumbu CYuugaru') = Kangaroo-Opossum-Iguana. Muri-Kubi ( VVutaru) = Emu-Bandicoot- Blacksnake. In the next generation : Ipai-Kumbu = Emu-Bandicoot-Blacksnake. Muri-Kubi = Kangaroo-Opossum-Iguana." This is incorrect. Ipai-Kumbu always^ Emu-Bandicoot-Blacksnakc and Muri-Kubi always = Kangaroo- Opossum-Iguana. The gentes, there- fore, do not " alternate between the original classes in alternate genera- tions." P. 52, line 2 of Latin quotation from " Eyre's Discoveries,"/'"' ^'pvoeiet" read "^praek'^." P. -
Temporal Lags and Overlap in the Diversification of Weevils and Flowering Plants
Temporal lags and overlap in the diversification of weevils and flowering plants Duane D. McKennaa,1, Andrea S. Sequeirab, Adriana E. Marvaldic, and Brian D. Farrella aDepartment of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA 02138; bDepartment of Biological Sciences, Wellesley College, Wellesley, MA 02481; and cInstituto Argentino de Investigaciones de Zonas Aridas, Consejo Nacional de Investigaciones Científicas y Te´cnicas, C.C. 507, 5500 Mendoza, Argentina Edited by May R. Berenbaum, University of Illinois at Urbana-Champaign, Urbana, IL, and approved March 3, 2009 (received for review October 22, 2008) The extraordinary diversity of herbivorous beetles is usually at- tributed to coevolution with angiosperms. However, the degree and nature of contemporaneity in beetle and angiosperm diversi- fication remain unclear. Here we present a large-scale molecular phylogeny for weevils (herbivorous beetles in the superfamily Curculionoidea), one of the most diverse lineages of insects, based on Ϸ8 kilobases of DNA sequence data from a worldwide sample including all families and subfamilies. Estimated divergence times derived from the combined molecular and fossil data indicate diversification into most families occurred on gymnosperms in the Jurassic, beginning Ϸ166 Ma. Subsequent colonization of early crown-group angiosperms occurred during the Early Cretaceous, but this alone evidently did not lead to an immediate and ma- jor diversification event in weevils. Comparative trends in weevil diversification and angiosperm dominance reveal that massive EVOLUTION diversification began in the mid-Cretaceous (ca. 112.0 to 93.5 Ma), when angiosperms first rose to widespread floristic dominance. These and other evidence suggest a deep and complex history of coevolution between weevils and angiosperms, including codiver- sification, resource tracking, and sequential evolution. -
ACT, Australian Capital 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. -
Threatened Species Protection Act 1995
Contents (1995 - 83) Threatened Species Protection Act 1995 Long Title Part 1 - Preliminary 1. Short title 2. Commencement 3. Interpretation 4. Objectives to be furthered 5. Administration of public authorities 6. Crown to be bound Part 2 - Administration 7. Functions of Secretary 8. Scientific Advisory Committee 9. Community Review Committee Part 3 - Conservation of Threatened Species Division 1 - Threatened species strategy 10. Threatened species strategy 11. Procedure for making strategy 12. Amendment and revocation of strategy Division 2 - Listing of threatened flora and fauna 13. Lists of threatened flora and fauna 14. Notification by Minister and right of appeal 15. Eligibility for listing 16. Nomination for listing 17. Consideration of nomination by SAC 18. Preliminary recommendation by SAC 19. Final recommendation by SAC 20. CRC to be advised of public notification 21. Minister's decision Division 3 - Listing statements 22. Listing statements Division 4 - Critical habitats 23. Determination of critical habitats 24. Amendment and revocation of determinations Division 5 - Recovery plans for threatened species 25. Recovery plans 26. Amendment and revocation of recovery plans Division 6 - Threat abatement plans 27. Threat abatement plans 28. Amendment and revocation of threat abatement plans Division 7 - Land management plans and agreements 29. Land management plans 30. Agreements arising from land management plans 31. Public authority management agreements Part 4 - Interim Protection Orders 32. Power of Minister to make interim protection orders 33. Terms of interim protection orders 34. Notice of order to landholder 35. Recommendation by Resource Planning and Development Commission 36. Notice to comply 37. Notification to other Ministers 38. Limitation of licences, permits, &c., issued under other Acts 39.