Foliage Insect Diversity in Dry Eucalypt Forests in Eastern Tasmania
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Wildlife Trade Operation Proposal – Queen of Ants
Wildlife Trade Operation Proposal – Queen of Ants 1. Title and Introduction 1.1/1.2 Scientific and Common Names Please refer to Attachment A, outlining the ant species subject to harvest and the expected annual harvest quota, which will not be exceeded. 1.3 Location of harvest Harvest will be conducted on privately owned land, non-protected public spaces such as footpaths, roads and parks in Victoria and from other approved Wildlife Trade Operations. Taxa not found in Victoria will be legally sourced from other approved WTOs or collected by Queen of Ants’ representatives from unprotected areas. This may include public spaces such as roadsides and unprotected council parks, and other property privately owned by the representatives. 1.4 Description of what is being harvested Please refer to Attachment A for an outline of the taxa to be harvested. The harvest is of live adult queen ants which are newly mated. 1.5 Is the species protected under State or Federal legislation Ants are non-listed invertebrates and are as such unprotected under Victorian and other State Legislation. Under Federal legislation the only protection to these species relates to the export of native wildlife, which this application seeks to satisfy. No species listed under the EPBC Act as threatened (excluding the conservation dependent category) or listed as endangered, vulnerable or least concern under Victorian legislation will be harvested. 2. Statement of general goal/aims The applicant has recently begun trading queen ants throughout Victoria as a personal hobby and has received strong overseas interest for the species of ants found. -
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. -
Dr. Sci. Roman Viktorovich Yakovlev Date Of
Dr. Sci. Roman Viktorovich Yakovlev Date of birth: November 30, 1974 Key words: fauna, entomology, systematics, Altai, Mongolia, Lepidoptera, Cossidae, Papilionoidea. Short biography Born in the city of Barnaul in the family of doctors. Graduated from school with a silver medal. 1996 - graduated from Altai State Medical Institute with the qualification "doctor". Worked as a child psychiatrist in the Altai Regional Psychoneurological Clinic. At the same time worked as a research associate in the South-Siberian Botanical Garden of Altai State University. Since 2014 - Doctor of Biological Sciences (specialty "Entomology", the theme of the dissertation: "Carpenter-Moths (Lepidoptera, Cossidae) of the Old World”); place of defense: Saint-Petersburg State University. 2008−2012 — Head of the Department at the Altai Regional Institute of Advanced Teachers Training. 2013−2014 − the vice-rector for the development of international activities of Altai State University. At present – senior researcher of Laboratory of Biodiversity and Ecology and assistant professor of the Department of Ecology, Biochemistry and Biotechnology at the Altai State University. Scientific specialization: systematics, faunistics and biogeography. Specialist in the following groups of Insecta: Papilionoidea, Sphingidae, Cossidae. Author of over 170 scientific papers (more than 30 of them indexed in Web of Science and Scopus. Described over 250 biological species as new for science. The first to have described the fauna of Cossidae of the following regions of the Earth: Russia, Vietnam, Mongolia, the Andaman Islands, the Korean Peninsula, Thailand, the Canary Islands, the island of Socotra, Zambia, Zimbabave, Malawi. Author of essays in the Red Book of the Altai Territory, the Altai Republic and the Republic of Khakassia. -
Microsoft Photo Editor
Environmental research on the impact of bumblebees in Australia and facilitation of national communication for and against further introductions Kaye Hergstrom Tasmanian Museum & Art Gallery Project Number: VG99033 VG99033 This report is published by Horticulture Australia Ltd to pass on information concerning horticultural research and development undertaken for the vegetable industry. The research contained in this report was funded by Horticulture Australia Ltd with the financial support of the vegetable industry and Hydroponic Farmers Federation. All expressions of opinion are not to be regarded as expressing the opinion of Horticulture Australia Ltd or any authority of the Australian Government. The Company and the Australian Government accept no responsibility for any of the opinions or the accuracy of the information contained in this report and readers should rely upon their own enquiries in making decisions concerning their own interests. ISBN 0 7341 0532 0 Published and distributed by: Horticulture Australia Ltd Level 1 50 Carrington Street Sydney NSW 2000 Telephone: (02) 8295 2300 Fax: (02) 8295 2399 E-Mail: [email protected] © Copyright 2002 Environmental Research on the Impact of Bumblebees in Australia and Facilitation of National Communication for/against Further Introduction Prepared by Kaye Hergstrom1, Roger Buttermore1, Owen Seeman2 and Bruce McCorkell2 1Tasmanian Museum and Art Gallery, 40 Macquarie St, Hobart Tas., 2Department of Primary Industries, Water and the Environment, Tas. 13 St Johns Ave, New Town, Tas. Horticulture Australia Project No: VG99033 The authors gratefully acknowledge the funding support provided by: Horticulture Australia Additional support in kind has been provided by: The Tasmanian Museum and Art Gallery Front cover illustration by Mike Tobias; design by Lexi Clark Any recommendations contained in this publication do not necessarily represent current HRDC policy. -
The Mcguire Center for Lepidoptera and Biodiversity
Supplemental Information All specimens used within this study are housed in: the McGuire Center for Lepidoptera and Biodiversity (MGCL) at the Florida Museum of Natural History, Gainesville, USA (FLMNH); the University of Maryland, College Park, USA (UMD); the Muséum national d’Histoire naturelle in Paris, France (MNHN); and the Australian National Insect Collection in Canberra, Australia (ANIC). Methods DNA extraction protocol of dried museum specimens (detailed instructions) Prior to tissue sampling, dried (pinned or papered) specimens were assigned MGCL barcodes, photographed, and their labels digitized. Abdomens were then removed using sterile forceps, cleaned with 100% ethanol between each sample, and the remaining specimens were returned to their respective trays within the MGCL collections. Abdomens were placed in 1.5 mL microcentrifuge tubes with the apex of the abdomen in the conical end of the tube. For larger abdomens, 5 mL microcentrifuge tubes or larger were utilized. A solution of proteinase K (Qiagen Cat #19133) and genomic lysis buffer (OmniPrep Genomic DNA Extraction Kit) in a 1:50 ratio was added to each abdomen containing tube, sufficient to cover the abdomen (typically either 300 µL or 500 µL) - similar to the concept used in Hundsdoerfer & Kitching (1). Ratios of 1:10 and 1:25 were utilized for low quality or rare specimens. Low quality specimens were defined as having little visible tissue inside of the abdomen, mold/fungi growth, or smell of bacterial decay. Samples were incubated overnight (12-18 hours) in a dry air oven at 56°C. Importantly, we also adjusted the ratio depending on the tissue type, i.e., increasing the ratio for particularly large or egg-containing abdomens. -
1 General Introduction
1 General Introduction If the karate-ka (student) shall walk the true path, first he will cast aside all preference. Tatsuo Shimabuku, Grand Master of Isshin-ryu Karate 1.1 The Importance of Insects ~30% of the plants we grow for food and materials. Because of their great numbers and diversity, insects Insects transmit some of these pathogens. While have a considerable impact on human life and indus- weeds can often reduce pest attack, they can also try, particularly away from cities and in the tropics. harbour the pest’s enemies or provide alternative On the positive side they form a large and irreplace- resources for the pest itself. Then in storage, insects, able part of the ecosystem, especially as pollinators mites, rodents and fungi cause a further 30% loss. of fruit and vegetable crops and, of course, many Apart from such biotic damage, severe physical con- wild plants (Section 8.2.1). They also have a place ditions such as drought, storms and flooding cause in soil formation (Section 8.2.4) and are being used additional losses. For example, under ideal field increasingly in ‘greener’ methods of pest control. conditions new wheat varieties (e.g. Agnote and Biological control using insects as predators and Humber) would give yields of ~16 tonnes/ha, but parasites of pest insects has been developed in the produce typically about half this under good hus- West for over a century, and much longer in China. bandry. Pre-harvest destruction due only to insects More recently integrated pest management (IPM) is 10–13% (Pimentel et al., 1984; Thacker, 2002). -
Report-VIC-Croajingolong National Park-Appendix A
Croajingolong National Park, Victoria, 2016 Appendix A: Fauna species lists Family Species Common name Mammals Acrobatidae Acrobates pygmaeus Feathertail Glider Balaenopteriae Megaptera novaeangliae # ~ Humpback Whale Burramyidae Cercartetus nanus ~ Eastern Pygmy Possum Canidae Vulpes vulpes ^ Fox Cervidae Cervus unicolor ^ Sambar Deer Dasyuridae Antechinus agilis Agile Antechinus Dasyuridae Antechinus mimetes Dusky Antechinus Dasyuridae Sminthopsis leucopus White-footed Dunnart Felidae Felis catus ^ Cat Leporidae Oryctolagus cuniculus ^ Rabbit Macropodidae Macropus giganteus Eastern Grey Kangaroo Macropodidae Macropus rufogriseus Red Necked Wallaby Macropodidae Wallabia bicolor Swamp Wallaby Miniopteridae Miniopterus schreibersii oceanensis ~ Eastern Bent-wing Bat Muridae Hydromys chrysogaster Water Rat Muridae Mus musculus ^ House Mouse Muridae Rattus fuscipes Bush Rat Muridae Rattus lutreolus Swamp Rat Otariidae Arctocephalus pusillus doriferus ~ Australian Fur-seal Otariidae Arctocephalus forsteri ~ New Zealand Fur Seal Peramelidae Isoodon obesulus Southern Brown Bandicoot Peramelidae Perameles nasuta Long-nosed Bandicoot Petauridae Petaurus australis Yellow Bellied Glider Petauridae Petaurus breviceps Sugar Glider Phalangeridae Trichosurus cunninghami Mountain Brushtail Possum Phalangeridae Trichosurus vulpecula Common Brushtail Possum Phascolarctidae Phascolarctos cinereus Koala Potoroidae Potorous sp. # ~ Long-nosed or Long-footed Potoroo Pseudocheiridae Petauroides volans Greater Glider Pseudocheiridae Pseudocheirus peregrinus -
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. -
Lepidoptera: Tortricidae: Tortricinae) and Evolutionary Correlates of Novel Secondary Sexual Structures
Zootaxa 3729 (1): 001–062 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Monograph ZOOTAXA Copyright © 2013 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3729.1.1 http://zoobank.org/urn:lsid:zoobank.org:pub:CA0C1355-FF3E-4C67-8F48-544B2166AF2A ZOOTAXA 3729 Phylogeny of the tribe Archipini (Lepidoptera: Tortricidae: Tortricinae) and evolutionary correlates of novel secondary sexual structures JASON J. DOMBROSKIE1,2,3 & FELIX A. H. SPERLING2 1Cornell University, Comstock Hall, Department of Entomology, Ithaca, NY, USA, 14853-2601. E-mail: [email protected] 2Department of Biological Sciences, University of Alberta, Edmonton, Canada, T6G 2E9 3Corresponding author Magnolia Press Auckland, New Zealand Accepted by J. Brown: 2 Sept. 2013; published: 25 Oct. 2013 Licensed under a Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0 JASON J. DOMBROSKIE & FELIX A. H. SPERLING Phylogeny of the tribe Archipini (Lepidoptera: Tortricidae: Tortricinae) and evolutionary correlates of novel secondary sexual structures (Zootaxa 3729) 62 pp.; 30 cm. 25 Oct. 2013 ISBN 978-1-77557-288-6 (paperback) ISBN 978-1-77557-289-3 (Online edition) FIRST PUBLISHED IN 2013 BY Magnolia Press P.O. Box 41-383 Auckland 1346 New Zealand e-mail: [email protected] http://www.mapress.com/zootaxa/ © 2013 Magnolia Press 2 · Zootaxa 3729 (1) © 2013 Magnolia Press DOMBROSKIE & SPERLING Table of contents Abstract . 3 Material and methods . 6 Results . 18 Discussion . 23 Conclusions . 33 Acknowledgements . 33 Literature cited . 34 APPENDIX 1. 38 APPENDIX 2. 44 Additional References for Appendices 1 & 2 . 49 APPENDIX 3. 51 APPENDIX 4. 52 APPENDIX 5. -
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. -
The Radiation of Satyrini Butterflies (Nymphalidae: Satyrinae): A
Zoological Journal of the Linnean Society, 2011, 161, 64–87. With 8 figures The radiation of Satyrini butterflies (Nymphalidae: Satyrinae): a challenge for phylogenetic methods CARLOS PEÑA1,2*, SÖREN NYLIN1 and NIKLAS WAHLBERG1,3 1Department of Zoology, Stockholm University, 106 91 Stockholm, Sweden 2Museo de Historia Natural, Universidad Nacional Mayor de San Marcos, Av. Arenales 1256, Apartado 14-0434, Lima-14, Peru 3Laboratory of Genetics, Department of Biology, University of Turku, 20014 Turku, Finland Received 24 February 2009; accepted for publication 1 September 2009 We have inferred the most comprehensive phylogenetic hypothesis to date of butterflies in the tribe Satyrini. In order to obtain a hypothesis of relationships, we used maximum parsimony and model-based methods with 4435 bp of DNA sequences from mitochondrial and nuclear genes for 179 taxa (130 genera and eight out-groups). We estimated dates of origin and diversification for major clades, and performed a biogeographic analysis using a dispersal–vicariance framework, in order to infer a scenario of the biogeographical history of the group. We found long-branch taxa that affected the accuracy of all three methods. Moreover, different methods produced incongruent phylogenies. We found that Satyrini appeared around 42 Mya in either the Neotropical or the Eastern Palaearctic, Oriental, and/or Indo-Australian regions, and underwent a quick radiation between 32 and 24 Mya, during which time most of its component subtribes originated. Several factors might have been important for the diversification of Satyrini: the ability to feed on grasses; early habitat shift into open, non-forest habitats; and geographic bridges, which permitted dispersal over marine barriers, enabling the geographic expansions of ancestors to new environ- ments that provided opportunities for geographic differentiation, and diversification. -
List of Moth Species April Lightsheet
Moth species recorded during April 2019 lightsheet Abantiades aphenges Glyphidoptera polymita Pernattia pusilla Abantiades hyalinatus Halone sejuncta Plesanemma fucata Abantiades labyrinthicus Halone sejuncta Poecilasthena pulchraria Achyra affinitalis Hednota sp. Pollanisus sp. Agriophara sp. Hellula hydralis Proteuxoa sp. Alapadna pauropis Hypobapta tachyhalotaria Proteuxoa tortisigna Anthela varia Idea costaria Pseudanapaea transvestita Arrade leucocosmalis Labdia chryselectra Psilosticha sp. Asura lydia Lecithocera imprudens Pterolocera leucocera Capusa sp. Lepidoscia characota Rhuma sp. Catoryctis subparallela Lepidoscia sp. Scioglyptis chionomera Chenuala heliapsis Lichenaula tholodes Scoliacma nana Chiriphe dichotoma Limnaecia camptosema Scoparia exhibitalis Chloroclystis metallospora Limnaecia sp. Softa concavata Chlorocoma dichloraria Lychnographa agaura Stathmopoda sp. Chlorocoma sp. Macrobathra chrysotoxa Stibaroma sp. Chlorocoma stereota Macrobathra desmotoma Syneora euboliaria Circopetes obtusata Metasia capnochroa Termessa gratiosa Cosmodes elegans Microdes squamulata Thalaina clara Crocanthes micradelpha Mimaglossa nauplialis Thalaina selenaea Crypsiphona ocultaria Mnesampela lenae Thallarcha phalarota Cryptoptila australana Monoctenia smerintharia Threnosia heminephes Culladia cuneiferellus Monoctenia sp. Thrincophora lignigerana Detounda leptoplasta Monopis crocicapitella Tigrioides alterna Discophlebia sp. Munychryia senicula Tortricinae sp. Dissomorphia australiaria Musotima nitidalis Trichiocercus sparshalli Epidesmia