Rapid Assessment of the Need for a Detailed Pest Risk Analysis for Musotima Nitidalis
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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. -
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 -
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). -
Monitoring Report Spring/Summer 2015 Contents
Wimbledon and Putney Commons Monitoring Report Spring/Summer 2015 Contents CONTEXT 1 A. SYSTEMATIC RECORDING 3 METHODS 3 OUTCOMES 6 REFLECTIONS AND RECOMMENDATIONS 18 B. BIOBLITZ 19 REFLECTIONS AND LESSONS LEARNT 21 C. REFERENCES 22 LIST OF FIGURES Figure 1 Location of The Plain on Wimbledon and Putney Commons 2 Figure 2 Experimental Reptile Refuge near the Junction of Centre Path and Somerset Ride 5 Figure 3 Contrasting Cut and Uncut Areas in the Conservation Zone of The Plain, Spring 2015 6/7 Figure 4 Notable Plant Species Recorded on The Plain, Summer 2015 8 Figure 5 Meadow Brown and white Admiral Butterflies 14 Figure 6 Hairy Dragonfly and Willow Emerald Damselfly 14 Figure 7 The BioBlitz Route 15 Figure 8 Vestal and European Corn-borer moths 16 LIST OF TABLES Table 1 Mowing Dates for the Conservation Area of The Plain 3 Table 2 Dates for General Observational Records of The Plain, 2015 10 Table 3 Birds of The Plain, Spring - Summer 2015 11 Table 4 Summary of Insect Recording in 2015 12/13 Table 5 Rare Beetles Living in the Vicinity of The Plain 15 LIST OF APPENDICES A1 The Wildlife and Conservation Forum and Volunteer Recorders 23 A2 Sward Height Data Spring 2015 24 A3 Floral Records for The Plain : Wimbledon and Putney Commons 2015 26 A4 The Plain Spring and Summer 2015 – John Weir’s General Reports 30 A5 a Birds on The Plain March to September 2015; 41 B Birds on The Plain - summary of frequencies 42 A6 ai Butterflies on The Plain (DW) 43 aii Butterfly long-term transect including The Plain (SR) 44 aiii New woodland butterfly transect -
Crambidae Biosecurity Occurrence Background Subfamilies Short Description Diagnosis
Diaphania nitidalis Chilo infuscatellus Crambidae Webworms, Grass Moths, Shoot Borers Biosecurity BIOSECURITY ALERT This Family is of Biosecurity Concern Occurrence This family occurs in Australia. Background The Crambidae is a large, diverse and ubiquitous family of moths that currently comprises 11,500 species globally, with at least half that number again undescribed. The Crambidae and the Pyralidae constitute the superfamily Pyraloidea. Crambid larvae are concealed feeders with a great diversity in feeding habits, shelter building and hosts, such as: leaf rollers, shoot borers, grass borers, leaf webbers, moss feeders, root feeders that shelter in soil tunnels, and solely aquatic life habits. Many species are economically important pests in crops and stored food products. Subfamilies Until recently, the Crambidae was treated as a subfamily under the Pyralidae (snout moths or grass moths). Now they form the superfamily Pyraloidea with the Pyralidae. The Crambidae currently consists of the following 14 subfamilies: Acentropinae Crambinae Cybalomiinae Glaphyriinae Heliothelinae Lathrotelinae Linostinae Midilinae Musotiminae Odontiinae Pyraustinae Schoenobiinae Scopariinae Spilomelinae Short Description Crambid caterpillars are generally cylindrical, with a semiprognathous head and only primary setae (Fig 1). They are often plainly coloured (Fig. 16, Fig. 19), but can be patterned with longitudinal stripes and pinacula that may give them a spotted appearance (Fig. 10, Fig. 11, Fig. 14, Fig. 22). Prolegs may be reduced in borers (Fig. 16). More detailed descriptions are provided below. This factsheet presents, firstly, diagnostic features for the Pyraloidea (Pyralidae and Crambidae) and then the Crambidae. Information and diagnostic features are then provided for crambids listed as priority biosecurity threats for northern Australia. -
Home Pre-Fire Moth Species List by Species
Species present before fire - by species Scientific Name Common Name Family Abantiades aphenges Hepialidae Abantiades hyalinatus Mustard Ghost Moth Hepialidae Abantiades labyrinthicus Hepialidae Acanthodela erythrosema Oecophoridae Acantholena siccella Oecophoridae Acatapaustus leucospila Nolidae Achyra affinitalis Cotton Web Spinner Crambidae Aeolochroma mniaria Geometridae Ageletha hemiteles Oecophoridae Aglaosoma variegata Notodontidae Agriophara discobola Depressariidae Agrotis munda Brown Cutworm Noctuidae Alapadna pauropis Erebidae Alophosoma emmelopis Erebidae Amata nigriceps Erebidae Amelora demistis Pointed Cape Moth Geometridae Amelora sp. Cape Moths Geometridae Antasia flavicapitata Geometridae Anthela acuta Common Anthelid Moth Anthelidae Anthela ferruginosa Anthelidae Anthela repleta Anthelidae Anthela sp. Anthelidae Anthela varia Variable Anthelid Anthelidae Antipterna sp. Oecophoridae Ardozyga mesochra Gelechiidae Ardozyga sp. Gelechiidae Ardozyga xuthias Gelechiidae Arhodia lasiocamparia Pink Arhodia Geometridae Arrade destituta Erebidae Arrade leucocosmalis Erebidae Asthenoptycha iriodes Tortricidae Asura lydia Erebidae Azelina biplaga Geometridae Barea codrella Oecophoridae Calathusa basicunea Nolidae Calathusa hypotherma Nolidae Capusa graodes Geometridae Capusa sp. Geometridae Carposina sp. Carposinidae Casbia farinalis Geometridae Casbia sp. Geometridae Casbia tanaoctena Geometridae Catacometes phanozona Oecophoridae Catoryctis subparallela Xyloryctidae Cernia amyclaria Geometridae Chaetolopha oxyntis Geometridae Chelepteryx -
Phytochemical Constituents and Pharmacological Activities of Plants from the Genus Adiantum : a Review
Pan et al Tropical Journal of Pharmaceutical Research October 2011; 10 (5): 681-692 © Pharmacotherapy Group, Faculty of Pharmacy, University of Benin, Benin City, 300001 Nigeria. All rights reserved . Available online at http://www.tjpr.org http://dx.doi.org/10.4314/tjpr.v10i5.18 Review Article Phytochemical Constituents and Pharmacological Activities of Plants from the Genus Adiantum : A Review 1 1 1 1 1 2 C Pan , YG Chen *, XY Ma , JH Jiang , F He and Y Zhang 1Department of Chemistry, Yunnan Normal University, Kunming 650500, 2School of Pharmacy, Kunming Medical College, Kunming 650031, China. Abstract Adiantum is a genus of ca. 200 species in the family Adiantaceae, distributed extensively across the world from cool temperate zones to hot tropical regions. A lot of Adiantum species have been used in traditional Chinese medicine to cure human and animal diseases including relief of internal heat or fever, enhancement of urination, removal of urinary calculus, and sundry other curative claims. Chemical studies have shown the presence of various classes of compounds, the main ones being triterpenoids, flavonoids, phenyl propanoids, steroids, alicyclic acids, lipids and long-chain compounds. The extract of this genus as well as pure compounds isolated from it have been demonstrated to possess multiple pharmacological activities such as analgesic, antinociceptive, anti-implantation, and antimicrobial activities. In this review, we have addressed the phytochemistry and pharmacological activities of the Adiantum species in order to collate existing information on this plant as well as highlight its multi-activity properties as a medicinal agent. Keywords: Adiantum species, Adiantaceae, Phytochemical constituents, Pharmacological activities. -
A. Whitei (Kenmore, May 19 15, White A424496 (BRI)
ASSOCIATION OF w.D- "REGISTERm BY AUSTRALIA POST - PUBLICATIOR NUMBER NBH 380gmU I LEADER : Peter Hind, 41 Miller Street, Mount Druitt, 2770. SECRETARY: Moreen Woollett, 3 Currawang Place, Como West, 2226. TREASURER: Joan Moore, 2 Gannett Street, Gladesville,2111. SPORE BANK: Jenny Thompson, 2 Albion Place, Engadine, 2233. Another year draws rapidily to an end and its time to remind members that fees fall due in January for the 1389 year. It is perhaps timely too to reflect on our Group's activities and to make a plea for more contributions from members, on this occasion not in a direct financial sense. There is benefit for most of us in knowing morer%' about the practicalities of propagating and cultivating our native ferns. All members have experienced successes and failures, please wr' so those experiences can be passed on to others through this Newsletter. Later in this issue there is a request -directed to members wha bought ferns at the recent Wildflower Exhibition iH Sydney ta report the results achieved. If you purchased ferns bcught-in at the time of the Exhibition we would greatly appreciate your help. This issue we welcome a new member-Ian Higgfins from Victoria. Ian has written and said that the following ferns are native to the Castlemaine area: Adiantum aethiopicum, Blechnum minus, B. nudum, Cheilanthes austrotenuifolia, Lastriopsis acuminata, W%~~OS~TQS rutifolius, Doodia media, Marsilea drumondiiMarsilea "(2lI'khtS foregoing are being grown by Ian- how many members wead lik% *Q bear from Ian about the conditions under which the CheilaSEbe~ Plurosorus rutifolius in particular are growing ),CkwbBX~~&&& sfaberi, L Pellaea falcata, Pteris tremula, Polystichum prolif&&.Ul As&enium r flabellafolium, Azolla filiculaides, Blechum chamber&,i, CakcAZa dubia,Cyathea australis, Pteridium esculentum and ~phioqlossum lusitanicum. -
Forest Health Technology Enterprise Team Biological Control of Invasive
Forest Health Technology Enterprise Team TECHNOLOGY TRANSFER Biological Control Biological Control of Invasive Plants in the Eastern United States Roy Van Driesche Bernd Blossey Mark Hoddle Suzanne Lyon Richard Reardon Forest Health Technology Enterprise Team—Morgantown, West Virginia United States Forest FHTET-2002-04 Department of Service August 2002 Agriculture BIOLOGICAL CONTROL OF INVASIVE PLANTS IN THE EASTERN UNITED STATES BIOLOGICAL CONTROL OF INVASIVE PLANTS IN THE EASTERN UNITED STATES Technical Coordinators Roy Van Driesche and Suzanne Lyon Department of Entomology, University of Massachusets, Amherst, MA Bernd Blossey Department of Natural Resources, Cornell University, Ithaca, NY Mark Hoddle Department of Entomology, University of California, Riverside, CA Richard Reardon Forest Health Technology Enterprise Team, USDA, Forest Service, Morgantown, WV USDA Forest Service Publication FHTET-2002-04 ACKNOWLEDGMENTS We thank the authors of the individual chap- We would also like to thank the U.S. Depart- ters for their expertise in reviewing and summariz- ment of Agriculture–Forest Service, Forest Health ing the literature and providing current information Technology Enterprise Team, Morgantown, West on biological control of the major invasive plants in Virginia, for providing funding for the preparation the Eastern United States. and printing of this publication. G. Keith Douce, David Moorhead, and Charles Additional copies of this publication can be or- Bargeron of the Bugwood Network, University of dered from the Bulletin Distribution Center, Uni- Georgia (Tifton, Ga.), managed and digitized the pho- versity of Massachusetts, Amherst, MA 01003, (413) tographs and illustrations used in this publication and 545-2717; or Mark Hoddle, Department of Entomol- produced the CD-ROM accompanying this book. -
PTERIDOLOGIST 2012 Contents: Volume 5 Part 5, 2012 Scale Insect Pests of Ornamental Ferns Grown Indoors in Britain
PTERIDOLOGIST 2012 Contents: Volume 5 Part 5, 2012 Scale insect pests of ornamental ferns grown indoors in Britain. Dr. Chris Malumphy 306 Familiar Ferns in a Far Flung Paradise. Georgina A.Snelling 313 Book Review: A Field Guide to the Flora of South Georgia. Graham Ackers 318 Survivors. Neill Timm 320 The Dead of Winter? Keeping Tree Ferns Alive in the U.K. Mike Fletcher 322 Samuel Salt. Snapshots of a Victorian Fern Enthusiast. Nigel Gilligan 327 New faces at the Spore Exchange. Brian and Sue Dockerill 331 Footnote: Musotima nitidalis - a fern-feeding moth new to Britain. Chris Malumphy 331 Leaf-mining moths in Britain. Roger Golding 332 Book Review: Ferns of Southern Africa. A Comprehensive Guide. Tim Pyner 335 Stem dichotomy in Cyathea australis. Peter Bostock and Laurence Knight 336 Mrs Puffer’s Marsh Fern. Graham Ackers 340 Young Ponga Frond. Guenther K. Machol 343 Polypodium Species and Hybrids in the Yorkshire Dales. Ken Trewren 344 A Challenge to all Fern Lovers! Jennifer M. Ide 348 Lycopodiums: Trials in Pot Cultivation. Jerry Copeland 349 Book Review: Fern Fever. Alec Greening 359 Fern hunting in China, 2010. Yvonne Golding 360 Stamp collecting. Martin Rickard 365 Dreaming of Ferns. Tim Penrose 366 Variation in Asplenium scolopendrium. John Fielding 368 The Case for Filmy Ferns. Kylie Stocks 370 Polystichum setiferum ‘Cristato-gracile’. Julian Reed 372 Why is Chris Page’s “Ferns” So Expensive? Graham Ackers 374 A Magificent Housefern - Goniophlebium Subauriculatum. Bryan Smith 377 A Bolton Collection. Jack Bouckley 378 360 Snails, Slugs, Grasshoppers and Caterpillars. Steve Lamont 379 Sphenomeris chinensis. -
Biosearch 2004 Report
Biosearch Nyika: Malawi 2004 Edited by Marianne J Overton FOREWORD Peter Overton It is ten years since the Biosearch Nyika project was first mooted and agreement with the Director of National Parks and Wildlife obtained for our exploration of the remoter parts of the Nyika National Park. Over this period the teams have focused mainly on the northern part of the park where patrolling has been very limited and our gathering of intelligence has been most helpful to the Nyika management. In 2004 we undertook the most challenging expedition to date, launched from the extreme north of the park at Uledi, a four-hour drive from Thazima. The team‟s first challenge was to cross the unbridged North Rukuru River with all their supplies. They then had to climb up the western escarpment of the Mpanda ridge to a point on the Mpero River, where they set up a Base Camp, from which to launch out on their surveys. The greatest achievement was to climb both Mpanda and Kawozya and discover the remote Bleak House, now derelict but offering stunning views over Lake Malawi and far beyond. At this point they could certainly claim to be in remote country since this old site is much talked about but very rarely seen by visitors. We have yet to have clear information about who built it, when and why. Perhaps it was a holiday „retreat‟ for Livingstonia or a staging post for missionaries who conducted business on the west of the Nyika National Park and into Zambia. In many ways this expedition was the pinnacle of logistical achievement. -
Spillover and Species Interactions Across Habitat Edges Between Managed and Natural Forests
SPILLOVER AND SPECIES INTERACTIONS ACROSS HABITAT EDGES BETWEEN MANAGED AND NATURAL FORESTS ____________________________________________________ A thesis submitted in partial fulfilment of the requirements for the Degree of Doctor of Philosophy at the University of Canterbury by Carol M. Frost ____________________________________________________ School of Biological Sciences University of Canterbury 2013 Table of Contents Table of Contents………………………………………………………………………...ii List of Tables………………………………………………………………………...…..vi List of Figures…………………………………………………………………………..vii Abstract………………………………………………………………………………...viii Acknowledgements……………………………………………………………………....x Chapter I: Introduction………………………………………………………………….1 1.1 Land-use change as the leading cause of biodiversity loss………………………….1 1.2 Biodiversity conservation versus agricultural production…………………………..2 1.3 Spillover edge effects as a mechanism of change in remnant natural ecosystems….3 1.4 Measuring ecological change: species interactions underlie ecosystem function…..5 1.5 Predicting indirect interactions……………………………………………………...6 1.6 Thesis objectives, study system, and outline………………………………………..9 Chapter II: Community-level spillover of natural enemies.........................................14 2.1 Abstract…………………………………………………………………………….14 2.2 Introduction………………………………………………………………………...15 2.3 Methods…………………………………………………………………………….18 2.3.1 Study system…………………………………………………………………...18 2.3.2 Sampling herbivore abundance and parasitism levels…………………………20 2.3.3 Measuring spillover of natural