The Victorian Naturalist Is Published Six Times Per Year by The

Total Page:16

File Type:pdf, Size:1020Kb

The Victorian Naturalist Is Published Six Times Per Year by The Published by The Field Naturalists Club of Victoria since 1884 From the Editors Of all living things, invertebrates make up by far the largest group. In the state of Victoria alone, there are estimated to be 50 000 to 80 000 species of invertebrates; this can be compared to only about 670 vertebrates in the same region. Ironically, this disparity in numerical representation is paralleled inversely by our level of knowledge—in general terms, we know considerably less about the more-numerous invertebrates than about vertebrates. This issue of 'Ihe Victorian Naturalist goes a little way toward redressing that imbalance, reporting work on a variety of invertebrate species. The issue is perhaps timely in another respect, in coming at the time of year that sees the greatest activity by many invertebrate species. Lack ot space has precluded the inclusion in this issue of ‘Guidelines for authors’ usually a feature of the December issue of this journal. It is intended that the Guidelines will be published in Febru- ary 2010. The Guidelines are available from the website at <www.fncv.org.au/vicnat.htm>. The Victorian Naturalist is published six times per year by the Field Naturalists Club of Victoria Inc Registered Office: FNCV, 1 Gardenia Street, Blackburn, Victoria 3130, Australia. Postal Address: FNCV, Locked Bag 3, Blackburn, Victoria 3130, Australia. Phone/Fax (03) 9877 9860; International Phone/Fax 61 3 9877 9860. email: [email protected] www.fncv.org.au Address correspondence to: The Editors, The Victorian Naturalist , Locked Bag 3, Blackburn, Victoria, Australia 3130. Phone: (03) 9877 9860. Email: [email protected] The opinions expressed in papers and book reviews published in The Victorian Naturalist are those of the authors and do not necessarily represent the views oi the FNCV. Copyright ot all original material published in 7he Victorian Naturalist remains with the author. Yearly Subscription Rates - The Field Naturalists Club of Victoria Inc Membership category Institutional Single $65 Libraries and Institutions Concessional (pensioner/Senior) $50 - within Australia $120 Family (at same address) $85 - overseas AUDI 30 Junior $18 Additional junior (same family) $6 Schools/Clubs $65 Student $25 (These rates apply as of 1 October 2008) All subscription enquiries should be sent to FNCV, Locked Bag 3, Blackburn, Victoria, Australia 3130. Phone/Fax 61 3 9877 9860. Email: [email protected] Front cover: St Andrews Cross Spider Argiope keyserlingii. Photo by Dan Carey Photography. Back cover: Ornate Ochre Trapezites genevieveae. Photo by Dan Carey Photography. Victorian Naturalist Volume 126 (6) 2009 December Editors: Anne Morton, Gary Presland, Maria Gibson Editorial Assistant: Virgil Hubregtse From the Editors 190 Research Report The Heath Sand-skipper Antipodia chaostola (Meyrick, 1888) (Lepidoptera: Hesperiidae) in Central Gippsland, Victoria, by John Wainer and Alan Yen 192 Contributions Some records of non -marine molluscs for Banks and eastern Bass Straits, Tasmania, by John Whinray 203 A flight and new distribution record of Antitrogus carnei Britton (Coleoptera: Scarabaeidae: Melolonthinae), by Ian Faithfull 207 Naturalist Note Silent lodgers and uninvited guests: arthropods found in a suburban house, by Virgil Hubregtse 210 Book Review Bugs Alive! A Guide to Keeping Australian Invertebrates by Alan Henderson , Deanna Henderson and Jessie Sinclair, reviewed by Alan Yen 214 Spiders: Learning to Love them, by Lynne Kelly, reviewed by Jian Yen 216 The Complete Field Guide to Stick and Leaf Insects of Australia, by Paul D Brock and Jack W Hasenpusch, reviewed by Melanie Archer 217 Moths of Victorian Part 1: Silk Moths and Allies - Bombycoidea by Peter Marriot, reviewed by Lucy Gibson 218 Floodplain Woodland Plants of North East Victoria: Identification of natives and weeds and practical weed management for bush regeneration projects, by Helen Curtis and Peter Curtis, reviewed by Angus Martin 219 ISSN 0042-5184 Research Reports The Heath Sand-skipper Antipodia chaostola (Meyrick, 1888) (Lepidoptera: Hesperiidae) in Central Gippsland, Victoria John Wainer and Alan Yen Invertebrate Survey Section, Museum Victoria, GPO Box 666E, Melbourne, Victoria 3001 Current address: Department of Primary Industries, Knoxfield Centre, Private Mail Bag 15, Fei ntree Gully Delivery Centre, Victoria 3156 Email: [email protected]; [email protected] Abstract Specimens of the Heath Sand-skipper butterfly Antipodia chaostola were found from only three locations in a survey in Central Gippsland in 1998. The preferred larval food plant, Thatch Saw-sedge Gahnia radula , is com- mon and widespread but the butterfly appears restricted to areas of Heathy Woodland, which is a very uncom- vegetation mon community generally occurring on gentle, north-facing lower slopes. The dominant eucalypt species are stringybarks and peppermints, which commonly are stunted and sparse due to the very infertile, yellowish, gradational soils. Female Heath Sand-skippers appear to favour small young plants or regrowth of Saw-sedge, following bushfires, for oviposit ion. As fire may be important or necessary for new growth of Saw- sedge, it consequently may be important or necessary for the persistence of the Heath Sand -skipper. Using a 9-12 year fuel reduction burn cycle, and staggering the burning of patches of the habitat in a mosaic pattern, seem necessary to provide a constant availability of appropriate habitat for the Heath Sand-skipper. (7 he Victo- rian Naturalist 1 26 (6), 2009, 1 92-202) Keywords: Thatch Saw-sedge, Gahnia radula , habitat, Heathy Woodland, bushfire Introduction The Heath Sand-skipper Antipodia chaostola is or nominated for listing as threatened under a medium-sized skipper, with a wingspan of ap- the Fauna and Flora Guarantee Act in Victoria, proximately 30 mm for males and 35 mm for although Crosby (1990a) suggested that this females it (Fig. 1). As is fast flying and dull col- might prove necessary. Sands and New (2002) oured, it is inconspicuous in flight. It is distin- regarded the Victorian subspecies, A. chaostola guished from its congeners by its orange-brown chares (Waterhouse 1933), as having no nation- colour, and differs from hesperilline and other al conservation significance. Couchman and trapezitine skippers by the presence of scattered Couchman (1977) considered the Tasmanian orange hindwing maculation, and in behaviour subspecies A. chaostola leucophaea (Couchman, by a more open -winged pose when resting in 1946) rare, and it is listed as endangered under sunshine (Atkins 1984). Larvae are unlikely the Tasmanian Threatened Species Protection Act to be confused with other butterfly species ex- 1995. ploiting the same food plant as they have an The principal aims of the present study were unusual habit of positioning head down in a to survey for the presence of A. chaostola in downward opening shelter, and have an unu- potentially suitable areas of Heathy Woodland, sual bright red prothorax (Grund 1988). Braby its preferred habitat, in central Gippsland, and et al (1997) coined the common name Heath to investigate the response of A. chaostola to Sand-skipper to replace the previously accepted fire. Recommendations then can be made for Chaostola Skipper. the most appropriate control burning manage- Antipodia chaostola is an uncommon or rare ment regimes in Heathy Woodland necessary species throughout its geographical range (Bra- to maintain habitat suitable to encourage the by 2000; Douglas 1993; Dunn et al 1994; Field butterfly’s persistence. 1995; Neyland 1994). Sands (1990) regarded the Biology species as endangered and included it in a cat- The genus Antipodia as currently recognised, egory he defined as generally widely distributed , contains three species (Braby but decreasing in abundance to the point where 2000). They are separated from nearby genera by a number their survival is threatened’. It has not been listed 192 The Victorian Naturalist Research Reports Fig. 1 . The Heath Sand-skipper Antipodia chaostola. Photo: Ross Field. of distinctive characteristics. One is their lar- 1998). Activity is reduced when conditions val habit of occupying and pupating in a head are windy or overcast (D Crosby pers. comm. downward position within downward opening 1998). Individuals will often sun themselves on shelters on their food plant. Saw-sedge Gahnia leaves in sheltered spots. Males defend terri- spp. (Braby 2000). Three shelters are normally tory from a perch on a prominent twig or leaf constructed by each larva as it grows (Quick to which they return after inspecting or attack- 1991). Other species assigned to close genera ing nearby flying insects. These occasionally are (e.g. Hesperilla and Motasingha) shelter and other skippers, and often include the Austral- pupate in an upright position. Another unusual ian Painted Lady Vanessa kershawi y or even the feature of A. chaostola is its two-year life cycle, a large, flower-feeding Jewel Beetle Stigmodera feature it shares with other members of the ge- macularia , both of which can be common dur- nus but with no other Australian skippers (Braby ing Spring months. The Heath Sand-skipper 2000). The larval stage lasts up to 20 months or feeds on nectar from a range of low bushes or more (Braby 2000). Atkins ( 1 984) reported that herbs including Common Rice Flower Pimelea A. chaostola tlies each year, and that there are no humilis , Prickly Teatree Leptospermum con- discernible constant differences between speci- tinentale Heath L. , Teatree myrsinoides , and mens in odd and even years. Their pale, striped Milkmaids Burchardia umbellaia. Males occa- head and bright red prothorax easily distinguish sionally have been observed flying near ridge- larvae of A. chaostola (Atkins 1984). tops (Atkins 1984). Females are less active than Adult butterflies can be found flying dur- males and flit close to the ground in the sun, ing October and November, and occasional or sit and sun on leaves, especially those of the specimens have been recorded in September larval food plant preferred in eastern Victoria, are and December. They generally active only Thatch Saw-sedge G.
Recommended publications
  • Runningpostman Newsletter of the Private Land Conservation Program
    The RunningPostman Newsletter of the Private Land Conservation Program April 2009 Building partnerships with landowners for the sustainable management Issue 4 and conservation of natural values across the landscape. ISSN 1835-6141 Department of The Running Postman • April 2009 Primary Industries and Water 1 2 The Running In Postman this Our newsletter is named after Issue a small twining plant that is widespread in Tasmanian dry forests (Kennedia prostrata). Message from the Program Manager 3 The Running Postman is published Living in a shared house, every action has a reaction 4 three times per year, and circulated Managing habitat for wildlife in privately owned reserves 5 to all the participants in the various Private Land Conservation Native grasslands - more than just grass 6 Program (PLCP) initiatives, as well Balancing conservation and production: A landowner’s perspective 7 as other interested groups and individuals. Creating bandicoot habitat - conservation in captivity 8 The PLCP Conservation Covenant Habitat for threatened species - the butterfly Chaostola skipper 9 partners, Land for Wildlife Protecting habitat - saving species 10 members, and signatories Log on and get more for your land 11 to Vegetation Management Agreements now extends to AGFEST 2009 12 over 1000 people. These people Protected Areas on Private Land Program 12 range from graziers and farmers Selling Property 12 with extensive operations in the Midlands, through to people with ten hectare bush blocks on the fringes of Hobart, with just about everything in between. More information regarding the PLCP (and an electronic version of The Running Postman) can be found on the Department of Primary Industries and Water The Running Postman is printed on Monza Satin recycled paper, derived from website: sustainable forests, elemental chlorine free pulp and certified environmental systems.
    [Show full text]
  • Special Issue3.7 MB
    Volume Eleven Conservation Science 2016 Western Australia Review and synthesis of knowledge of insular ecology, with emphasis on the islands of Western Australia IAN ABBOTT and ALLAN WILLS i TABLE OF CONTENTS Page ABSTRACT 1 INTRODUCTION 2 METHODS 17 Data sources 17 Personal knowledge 17 Assumptions 17 Nomenclatural conventions 17 PRELIMINARY 18 Concepts and definitions 18 Island nomenclature 18 Scope 20 INSULAR FEATURES AND THE ISLAND SYNDROME 20 Physical description 20 Biological description 23 Reduced species richness 23 Occurrence of endemic species or subspecies 23 Occurrence of unique ecosystems 27 Species characteristic of WA islands 27 Hyperabundance 30 Habitat changes 31 Behavioural changes 32 Morphological changes 33 Changes in niches 35 Genetic changes 35 CONCEPTUAL FRAMEWORK 36 Degree of exposure to wave action and salt spray 36 Normal exposure 36 Extreme exposure and tidal surge 40 Substrate 41 Topographic variation 42 Maximum elevation 43 Climate 44 Number and extent of vegetation and other types of habitat present 45 Degree of isolation from the nearest source area 49 History: Time since separation (or formation) 52 Planar area 54 Presence of breeding seals, seabirds, and turtles 59 Presence of Indigenous people 60 Activities of Europeans 63 Sampling completeness and comparability 81 Ecological interactions 83 Coups de foudres 94 LINKAGES BETWEEN THE 15 FACTORS 94 ii THE TRANSITION FROM MAINLAND TO ISLAND: KNOWNS; KNOWN UNKNOWNS; AND UNKNOWN UNKNOWNS 96 SPECIES TURNOVER 99 Landbird species 100 Seabird species 108 Waterbird
    [Show full text]
  • Nota Lepidopterologica
    ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Nota lepidopterologica Jahr/Year: 2002 Band/Volume: 25 Autor(en)/Author(s): Garcia-Barros Enrique Artikel/Article: Taxonomic patterns in the egg to body size allometry of butterflies and skippers (Papilionoidea & Hesperiidae) 161-175 ©Societas Europaea Lepidopterologica; download unter http://www.biodiversitylibrary.org/ und www.zobodat.at Nota lepid. 25 (2/3): 161-175 161 Taxonomic patterns in the egg to body size allometry of butter- flies and skippers (Papilionoidea & Hesperiidae) Enrique Garcia-Barros Departmento de Biologia (Zool.), Universidad Autönoma de Madrid, E-28049 Madrid, Spain e-mail: [email protected] Summary. Former studies have shown that there is an interspecific allometric relationship between egg size and adult body size in butterflies and skippers. This is here re-assessed at the family and subfamily levels in order to determine to what extent the overall trend is uniform through different taxonomic lineages. The results suggest that different subtaxa are characterised by different allometric slopes. Al- though statistical analysis across species means is known to be potentially misleading to assess evolu- tionary relations, it is shown that the comparison of apparent patterns (based on species means) with inferred evolutionary trends (based on independent contrasts) may help to understand the evolution of egg size in butterflies. Further, intuitive reconsideration of statistically non-significant results may prove informative. As an example, argumentation in favour of a positive association between large egg size and the use of monocotyledon plants as larval food is presented. Taxa where atypical allometric trends are found include the Riodininae and Theclini (Lycaenidae), the Graphiini (Papilionidae), and the Heliconiinae (Nymphalidae).
    [Show full text]
  • Science for Saving Species Research Findings Factsheet Project 2.1
    Science for Saving Species Research findings factsheet Project 2.1 Butterflies on the brink: identifying the Australian butterflies most at risk of extinction In brief Background Terrestrial invertebrates and their Invertebrates are declining globally in high (greater than 30%) chance of habitats are increasingly threatened both diversity and abundance, with extinction. We also identified key by human disturbances, particularly potentially serious consequences threatening processes affecting habitat loss and fragmentation, for ecosystem functioning. Many these species (chiefly inappropriate invasive species, inappropriate fire Australian butterflies are imperilled fire regimes, habitat loss and regimes and climate change. or declining but few are listed fragmentation, invasive species and Continuing declines and extinctions for protection by legislation. climate change), and the research in native terrestrial invertebrate We identified the 26 Australian and management actions needed communities are likely to negatively butterflies at most immediate risk to save them. Mapping of the 26 affect ecosystem functioning. This is of extinction within a 20-year time butterflies’ distributions revealed that because invertebrates play a central frame. We found that one butterfly most are now found only in a single role in many ecological processes, is facing a greater than 90% chance state or territory and many occupy including pollination, herbivory, the of extinction in the next 20 years narrow ranges. Increased resourcing consumption of dead plant and (and may already be extinct), and and management intervention is animal matter, and nutrient cycling, four species have a moderate to required to avert future extinctions. as well as providing a good source of food for other animals. There is urgent need to explore the causes of these declines, and the implications for ecosystems and ecosystem services.
    [Show full text]
  • Phylogenetic Relationships of Subfamilies and Circumscription of Tribes in the Family Hesperiidae (Lepidoptera: Hesperioidea)
    Cladistics Cladistics 24 (2008) 642–676 10.1111/j.1096-0031.2008.00218.x Phylogenetic relationships of subfamilies and circumscription of tribes in the family Hesperiidae (Lepidoptera: Hesperioidea) Andrew D. Warrena,b,*, Joshua R. Ogawac and Andrew V. Z. Browerc aMcGuire Center for Lepidoptera and Biodiversity, Florida Museum of Natural History, University of Florida, SW 34th Street and Hull Road, PO Box 112710, Gainesville, FL 32611-2710, USA; bMuseo de Zoologı´a, Departamento de Biologı´a Evolutiva, Facultad de Ciencias, Universidad Nacional Auto´noma de Me´xico, Apdo. Postal 70-399, Me´xico DF 04510, Me´xico; cDepartment of Biology, Middle Tennessee State University, Murfreesboro, TN 37132, USA Accepted 10 January 2008 Abstract A comprehensive tribal-level classification for the worldÕs subfamilies of Hesperiidae, the skipper butterflies, is proposed for the first time. Phylogenetic relationships between tribes and subfamilies are inferred using DNA sequence data from three gene regions (cytochrome oxidase subunit I-subunit II, elongation factor-1a and wingless). Monophyly of the family is strongly supported, as are some of the traditionally recognized subfamilies, with the following relationships: (Coeliadinae + (‘‘Pyrginae’’ + (Heteropteri- nae + (Trapezitinae + Hesperiinae)))). The subfamily Pyrginae of contemporary authors was recovered as a paraphyletic grade of taxa. The formerly recognized subfamily Pyrrhopyginae, although monophyletic, is downgraded to a tribe of the ‘‘Pyrginae’’. The former subfamily Megathyminae is an infra-tribal group of the Hesperiinae. The Australian endemic Euschemon rafflesia is a hesperiid, possibly related to ‘‘Pyrginae’’ (Eudamini). Most of the traditionally recognized groups and subgroups of genera currently employed to partition the subfamilies of the Hesperiidae are not monophyletic.
    [Show full text]
  • From Mainland Southeastern Australia, with Ar
    © The Authors, 2018. Journal compilation © Australian Museum, Sydney, 2018 Records of the Australian Museum (2018) Vol. 70, issue number 5, pp. 423–433. ISSN 0067-1975 (print), ISSN 2201-4349 (online) https://doi.org/10.3853/j.2201-4349.70.2018.1715 urn:lsid:zoobank.org:pub:62503ED7-0C67-4484-BCE7-E4D81E54A41B Michael F. Braby orcid.org/0000-0002-5438-587X A new subspecies of Neolucia hobartensis (Miskin, 1890) (Lepidoptera: Lycaenidae) from Mainland Southeastern Australia, with a Review of Butterfly Endemism in Montane Areas in this Region Michael F. Braby1* and Graham E. Wurtz2 1 Division of Ecology and Evolution, Research School of Biology, The Australian National University, Acton ACT 2601, Australia, and National Research Collections Australia, Australian National Insect Collection, GPO Box 1700, Canberra ACT 2601, Australia 2 Thurgoona NSW 2640, Australia [email protected] Abstract. Neolucia hobartensis albolineata ssp. nov. is illustrated, diagnosed, described and compared with the nominate subspecies N. hobartensis hobartensis (Miskin, 1890) from Tasmania and N. hobartensis monticola Waterhouse & Lyell, 1914 from northern New South Wales, Australia. The new subspecies is restricted to montane areas (mainly >1000 m) in subalpine and alpine habitats on the mainland in southeastern Australia (southern NSW, ACT, VIC) where its larvae specialize on Epacris spp. (Ericaceae). It thus belongs to a distinct set of 22 butterfly taxa that are endemic and narrowly restricted to montane areas (>600 m, but mainly >900 m) on the tablelands and plateaus of mainland southeastern Australia. Monitoring of these taxa, including N. hobartensis ssp., is urgently required to assess the extent to which global climate change, particularly temperature rise and large-scale fire regimes, are key threatening processes.
    [Show full text]
  • The Mitogenome of a Malagasy Butterfly Malaza Fastuosus (Mabille
    Title The mitogenome of a Malagasy butterfly Malaza fastuosus (Mabille, 1884) recovered from the holotype collected over 140 years ago adds support for a new subfamily of Hesperiidae (Lepidoptera) Authors Zhang, J; Lees, David; Shen, J; Cong, Q; Huertas, B; Martin, G; Grishin, NV 195 ARTICLE The mitogenome of a Malagasy butterfly Malaza fastuosus (Mabille, 1884) recovered from the holotype collected over 140 years ago adds support for a new subfamily of Hesperiidae (Lepidoptera) Jing Zhang, David C. Lees, Jinhui Shen, Qian Cong, Blanca Huertas, Geoff Martin, and Nick V. Grishin Abstract: Malaza fastuosus is a lavishly patterned skipper butterfly from a genus that has three described species, all endemic to the mainland of Madagascar. To our knowledge, M. fastuosus has not been collected for nearly 50 years. To evaluate the power of our techniques to recover DNA, we used a single foreleg of an at least 140-year-old holotype specimen from the collection of the Natural History Museum London with no destruction of external morphology to extract DNA and assemble a complete mitogenome from next generation sequencing reads. The resulting 15 540 bp mitogenome contains 13 protein-coding genes, 22 transfer RNA genes, two ribosomal RNA genes, and an A+T rich region, similarly to other Lepidoptera mitogenomes. Here we provide the first mitogenome also for Trapezitinae (Rachelia extrusus). Phylogenetic analysis of available skipper mitogenomes places Malaza outside of Trapezitinae and Barcinae + Hesperiinae, with a possible sister relationship to Heteropterinae. Of these, at least Heteropterinae, Trape- zitinae, and almost all Hesperiinae have monocot-feeding caterpillars. Malaza appears to be an evolutionarily highly distinct ancient lineage, morphologically with several unusual hesperiid features.
    [Show full text]
  • 2013 Rubenstein Research Fellows Papilionoidea of the World
    2013 Rubenstein Research Fellows Papilionoidea of the World: Evaluation and validation of EOL and BHL data for Hesperiidae JR Ferrer-Paris, AY S´anchez-Mercado, C Lozano, L Zambrano, J Soto, J Baettig and P Ortega Centro de Estudios Bot´anicos y Agroforestales Instituto Venezolano de Investigaciones Cient´ıficas Report EOLR.r.2013.10 available at the PoW home page Version of 13 de noviembre de 2013 CC BY-NC 3.0,Some rights reserved Abstract We evaluate the representativeness of two open sources of data for the butterfly family Hesperiidae that represent almost 20 % of the known species of butterflies (Papilionoidea). First we built a taxonomic checklist from available information and ordered the species lists according to a preliminary phylogeny. Checklists are based on the most updated and com- plete synonimic list and catalogues available in public sources, and phylogenies are based on approximated phylogenies for several clades within the family. For each species we retrieved all available text data objects from the Encyclopedia of Life, EOL and all pages from the Biodiversity Heritage Library, BHL. We then analyse the distribution of data objects, pages and records per species and the representativeness of each data source accross the phylogeny, and compare them with the results obtained for other families. Hesperiidae are poorly represented in both sources, available content was generally lower and less rich than for Papilionidae and Pieridae, and not much better than for Riodinidae. Differences between hesperid subfamilies were evident, but not extrem, with Eudaminae, Coeliadinae and Trapetizinae slightly better represented. In EOL, the main contributors are 1 associated with phylogenetic and molecular data providers, and fewer data objects about their biology and ecology.
    [Show full text]
  • Papers and Proceedings of the Royal Society of Tasmania
    140 A NEW TASMANIAN BUTTERFLY AND A LIST OF THE KNOWN TASMANIAN SPECIES. By G. H. Hardy. (Received Utli August, 1916. Read 21st August, 1916. Issued separately 3 1st August, 1916.) Oreixenica flynni, sp. nov. Female. Black-brown. Forewing with three basal spots (consisling of two large spots in the cell, the second beins: confluent with the third, situated at the base of area la.), and a band of irregular discal spots uniformly distant from the basal spots, gold-brown. A band of ir- regular subapical spots reaching to vein 3, containing two unequal black ocelli, red-brown, and a series of small sub- terminal spots, gold-brown. Hindwing with a series of basal and subtenuiiial spots, <?old-l>rowii ; discnl spols goli- brown, and some suffused with red brown, and a subtornal ocellus black. Underside; forewing as in 0. orichora, but a smaller second ocellus is present, and the whitish subtenninal spot* are smaller. Hindwing differs from 0. orichora only by the smaller whitish spots, and the slightly smaller subapical and subtornal ocelli. The species is undoubtedly a Tasmanian race of 0. orichora from Victoria, and New South Wales, from which the female differs chiefly in the forewing, having tho space between the basal spots and dincal spots uniformly wide. Width across Mangs 29 mm. Hab. Cradle Mountain, Tasmania., 3,00Gft. 1 speci- men taken by Prof. T. T. Flynn. Christmas, 1915. In the same locality Prof. Flynn also took Neo.renica teprea {Heiuit^) and Arrjynnina toHmanica (Lycll), the first being previously only known from Mt. Wellington, and the latter from the West Coast.
    [Show full text]
  • A Special Ridge – Andrew Atkins
    A Special Ridge – Andrew Atkins ‘Unthinking, you drift into a memory landscape of deeply living activity: all about the song and colour of nature; boundless micro-stories of survival, instinct and passion’. Anon. Cover plate Everyone experiences those rushes of blood, racing heartbeats and the unhidden joy when exploring new landscapes; just a touch of apprehension bound with inquisitiveness, perhaps brashness; an explorer’s motivation - a naturalist’s excitement. Memories abound, but for me, those most indelible are the collecting days at Blackdown Tableland, Central Queensland: the sun’s spreading intensity, harsh bush calls, weary walks amid a sometimes hostile understory, but beautifully challenging. Add the wildlife, the early summer storms, remoteness - and azure butterflies spinning in the sky. Warm early morning thermals lofted the Cessna easily to 3,000 metres. This was early 1970, and, as part of Australian Broadcasting, Rockhampton Queensland (ABRQ-9) film production unit, we were heading to Emerald to do a ‘doco’ on quarter horses. Just under the forty-minute flight a majestic sloping arrowhead of highlands appeared to the south. The pilot leaned across “Expedition Range - sandstone country, discovered by Ludwig Leichhardt in 1847” he said. Now soaring above the highest northern tip, a pale creamy-orange steep ridge of cliffs, cut by narrow, violet gorges breached above a surrounding ocean of blue-grey brigalow woodland. An instant moment of recall: those past, productive ‘sand stone’ field trips to the Grampians and the Blue Mountains to the distant south. This range looks butterfly-friendly! Filming done (there was no video-tape in those days), we returned in the late haze.
    [Show full text]
  • Rangelands, Western Australia
    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.
    [Show full text]
  • South Australian Arid Lands, South Australia
    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.
    [Show full text]