Industry Environmental Offset Funding Facilitates a Large Multi-Species Fauna Translocation Program
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Macropod Herpesviruses Dec 2013
Herpesviruses and macropods Fact sheet Introductory statement Despite the widespread distribution of herpesviruses across a large range of macropod species there is a lack of detailed knowledge about these viruses and the effects they have on their hosts. While they have been associated with significant mortality events infections are usually benign, producing no or minimal clinical effects in their adapted hosts. With increasing emphasis being placed on captive breeding, reintroduction and translocation programs there is a greater likelihood that these viruses will be introduced into naïve macropod populations. The effects and implications of this type of viral movement are unclear. Aetiology Herpesviruses are enveloped DNA viruses that range in size from 120 to 250nm. The family Herpesviridae is divided into three subfamilies. Alphaherpesviruses have a moderately wide host range, rapid growth, lyse infected cells and have the capacity to establish latent infections primarily, but not exclusively, in nerve ganglia. Betaherpesviruses have a more restricted host range, a long replicative cycle, the capacity to cause infected cells to enlarge and the ability to form latent infections in secretory glands, lymphoreticular tissue, kidneys and other tissues. Gammaherpesviruses have a narrow host range, replicate in lymphoid cells, may induce neoplasia in infected cells and form latent infections in lymphoid tissue (Lachlan and Dubovi 2011, Roizman and Pellet 2001). There have been five herpesvirus species isolated from macropods, three alphaherpesviruses termed Macropodid Herpesvirus 1 (MaHV1), Macropodid Herpesvirus 2 (MaHV2), and Macropodid Herpesvirus 4 (MaHV4) and two gammaherpesviruses including Macropodid Herpesvirus 3 (MaHV3), and a currently unclassified novel gammaherpesvirus detected in swamp wallabies (Wallabia bicolor) (Callinan and Kefford 1981, Finnie et al. -
A Phylogeny and Timescale for Marsupial Evolution Based on Sequences for Five Nuclear Genes
J Mammal Evol DOI 10.1007/s10914-007-9062-6 ORIGINAL PAPER A Phylogeny and Timescale for Marsupial Evolution Based on Sequences for Five Nuclear Genes Robert W. Meredith & Michael Westerman & Judd A. Case & Mark S. Springer # Springer Science + Business Media, LLC 2007 Abstract Even though marsupials are taxonomically less diverse than placentals, they exhibit comparable morphological and ecological diversity. However, much of their fossil record is thought to be missing, particularly for the Australasian groups. The more than 330 living species of marsupials are grouped into three American (Didelphimorphia, Microbiotheria, and Paucituberculata) and four Australasian (Dasyuromorphia, Diprotodontia, Notoryctemorphia, and Peramelemorphia) orders. Interordinal relationships have been investigated using a wide range of methods that have often yielded contradictory results. Much of the controversy has focused on the placement of Dromiciops gliroides (Microbiotheria). Studies either support a sister-taxon relationship to a monophyletic Australasian clade or a nested position within the Australasian radiation. Familial relationships within the Diprotodontia have also proved difficult to resolve. Here, we examine higher-level marsupial relationships using a nuclear multigene molecular data set representing all living orders. Protein-coding portions of ApoB, BRCA1, IRBP, Rag1, and vWF were analyzed using maximum parsimony, maximum likelihood, and Bayesian methods. Two different Bayesian relaxed molecular clock methods were employed to construct a timescale for marsupial evolution and estimate the unrepresented basal branch length (UBBL). Maximum likelihood and Bayesian results suggest that the root of the marsupial tree is between Didelphimorphia and all other marsupials. All methods provide strong support for the monophyly of Australidelphia. Within Australidelphia, Dromiciops is the sister-taxon to a monophyletic Australasian clade. -
Habitat Conservation Plan a Plan for the Protection of the Perdido Key
Perdido Key Programmatic Habitat Conservation Plan Escambia County, Florida HABITAT CONSERVATION PLAN A PLAN FOR THE PROTECTION OF THE PERDIDO KEY BEACH MOUSE, SEA TURTLES, AND PIPING PLOVERS ON PERDIDO KEY, FLORIDA Prepared in Support of Incidental Take Permit No. for Incidental Take Related to Private Development and Escambia County Owned Land and Infrastructure Improvements on Perdido Key, Florida Prepared for: ESCAMBIA COUNTY BOARD OF COUNTY COMMISSIONERS P.O. BOX 1591 PENSACOLA, FL 32591 Prepared by: PBS&J 2401 EXECUTIVE PLAZA, SUITE 2 PENSACOLA, FLORIDA 32504 Submitted to: U.S. FISH AND WILDLIFE SERVICE ECOLOGICAL SERVICES & FISHERIES RESOURCES OFFICE 1601 BALBOA AVENUE PANAMA CITY, FLORIDA 32450 Final Draft January 2010 Draft Submitted December 2008 Draft Revised March 2009 Draft Revised May 2009 Draft Revised October 2009 ii Perdido Key Programmatic Habitat Conservation Plan Escambia County, Florida TABLE OF CONTENTS ABBREVIATIONS ........................................................................................................ viii LIST OF TABLES ............................................................................................................ x LIST OF APPENDICES ................................................................................................. xi EXECUTIVE SUMMARY ............................................................................................ xii 1.0 INTRODUCTION....................................................................................................... 1 1.1 Background -
Translocations and Fauna Reconstruction Sites: Western Shield Review—February 2003
108 Conservation Science W. Aust. 5 (2) : 108–121P.R. Mawson (2004) Translocations and fauna reconstruction sites: Western Shield review—February 2003 PETER R. MAWSON1 1Senior Zoologist, Wildlife Branch , Department of Conservation and Land Management, Locked Bag 104 Bentley Delivery Centre WA 6983. [email protected] SUMMARY address this problem, but will result in slower progress towards future milestones for some species. The captive-breeding of western barred bandicoots Objectives has also been hampered by disease issues, but this problem is dealt with in more detail elsewhere in this edition (see The objectives of Western Shield with regard to fauna Morris et al. this issue). translocations were to re-introduce a range of native fauna There is a clear need to better define criteria that will species to a number of sites located primarily in the south- be used to determine the success or failure of translocation west of Western Australia. At some sites whole suites of programs, and for those same criteria to be included in fauna needed to be re-introduced, while at others only Recovery Plans and Interim Recovery Plans. one or a few species were targeted for re-introduction. A small number of the species that are currently the Integration of Western Shield activities with recovery subject of captive-breeding programs and or translocations actions and co-operative arrangements with community do not have Recovery Plans or Interim Recovery Plans, groups, wildlife carers, wildlife sanctuaries, Perth Zoo and contrary to CALM Policy Statement No. 50. In other educational outcomes were other key objectives. cases the priorities by which plans are written does not Achievements reflect the IUCN rank assigned those species by the Western Australian Threatened Species Scientific The fauna translocation objectives defined in the founding Committee. -
A Species-Level Phylogenetic Supertree of Marsupials
J. Zool., Lond. (2004) 264, 11–31 C 2004 The Zoological Society of London Printed in the United Kingdom DOI:10.1017/S0952836904005539 A species-level phylogenetic supertree of marsupials Marcel Cardillo1,2*, Olaf R. P. Bininda-Emonds3, Elizabeth Boakes1,2 and Andy Purvis1 1 Department of Biological Sciences, Imperial College London, Silwood Park, Ascot SL5 7PY, U.K. 2 Institute of Zoology, Zoological Society of London, Regent’s Park, London NW1 4RY, U.K. 3 Lehrstuhl fur¨ Tierzucht, Technical University of Munich, Alte Akademie 12, 85354 Freising-Weihenstephan, Germany (Accepted 26 January 2004) Abstract Comparative studies require information on phylogenetic relationships, but complete species-level phylogenetic trees of large clades are difficult to produce. One solution is to combine algorithmically many small trees into a single, larger supertree. Here we present a virtually complete, species-level phylogeny of the marsupials (Mammalia: Metatheria), built by combining 158 phylogenetic estimates published since 1980, using matrix representation with parsimony. The supertree is well resolved overall (73.7%), although resolution varies across the tree, indicating variation both in the amount of phylogenetic information available for different taxa, and the degree of conflict among phylogenetic estimates. In particular, the supertree shows poor resolution within the American marsupial taxa, reflecting a relative lack of systematic effort compared to the Australasian taxa. There are also important differences in supertrees based on source phylogenies published before 1995 and those published more recently. The supertree can be viewed as a meta-analysis of marsupial phylogenetic studies, and should be useful as a framework for phylogenetically explicit comparative studies of marsupial evolution and ecology. -
Factsheet: a Threatened Mammal Index for Australia
Science for Saving Species Research findings factsheet Project 3.1 Factsheet: A Threatened Mammal Index for Australia Research in brief How can the index be used? This project is developing a For the first time in Australia, an for threatened plants are currently Threatened Species Index (TSX) for index has been developed that being assembled. Australia which can assist policy- can provide reliable and rigorous These indices will allow Australian makers, conservation managers measures of trends across Australia’s governments, non-government and the public to understand how threatened species, or at least organisations, stakeholders and the some of the population trends a subset of them. In addition to community to better understand across Australia’s threatened communicating overall trends, the and report on which groups of species are changing over time. It indices can be interrogated and the threatened species are in decline by will inform policy and investment data downloaded via a web-app to bringing together monitoring data. decisions, and enable coherent allow trends for different taxonomic It will potentially enable us to better and transparent reporting on groups or regions to be explored relative changes in threatened understand the performance of and compared. So far, the index has species numbers at national, state high-level strategies and the return been populated with data for some and regional levels. Australia’s on investment in threatened species TSX is based on the Living Planet threatened and near-threatened birds recovery, and inform our priorities Index (www.livingplanetindex.org), and mammals, and monitoring data for investment. a method developed by World Wildlife Fund and the Zoological A Threatened Species Index for mammals in Australia Society of London. -
Wildlife Parasitology in Australia: Past, Present and Future
CSIRO PUBLISHING Australian Journal of Zoology, 2018, 66, 286–305 Review https://doi.org/10.1071/ZO19017 Wildlife parasitology in Australia: past, present and future David M. Spratt A,C and Ian Beveridge B AAustralian National Wildlife Collection, National Research Collections Australia, CSIRO, GPO Box 1700, Canberra, ACT 2601, Australia. BVeterinary Clinical Centre, Faculty of Veterinary and Agricultural Sciences, University of Melbourne, Werribee, Vic. 3030, Australia. CCorresponding author. Email: [email protected] Abstract. Wildlife parasitology is a highly diverse area of research encompassing many fields including taxonomy, ecology, pathology and epidemiology, and with participants from extremely disparate scientific fields. In addition, the organisms studied are highly dissimilar, ranging from platyhelminths, nematodes and acanthocephalans to insects, arachnids, crustaceans and protists. This review of the parasites of wildlife in Australia highlights the advances made to date, focussing on the work, interests and major findings of researchers over the years and identifies current significant gaps that exist in our understanding. The review is divided into three sections covering protist, helminth and arthropod parasites. The challenge to document the diversity of parasites in Australia continues at a traditional level but the advent of molecular methods has heightened the significance of this issue. Modern methods are providing an avenue for major advances in documenting and restructuring the phylogeny of protistan parasites in particular, while facilitating the recognition of species complexes in helminth taxa previously defined by traditional morphological methods. The life cycles, ecology and general biology of most parasites of wildlife in Australia are extremely poorly understood. While the phylogenetic origins of the Australian vertebrate fauna are complex, so too are the likely origins of their parasites, which do not necessarily mirror those of their hosts. -
Ba3444 MAMMAL BOOKLET FINAL.Indd
Intot Obliv i The disappearing native mammals of northern Australia Compiled by James Fitzsimons Sarah Legge Barry Traill John Woinarski Into Oblivion? The disappearing native mammals of northern Australia 1 SUMMARY Since European settlement, the deepest loss of Australian biodiversity has been the spate of extinctions of endemic mammals. Historically, these losses occurred mostly in inland and in temperate parts of the country, and largely between 1890 and 1950. A new wave of extinctions is now threatening Australian mammals, this time in northern Australia. Many mammal species are in sharp decline across the north, even in extensive natural areas managed primarily for conservation. The main evidence of this decline comes consistently from two contrasting sources: robust scientifi c monitoring programs and more broad-scale Indigenous knowledge. The main drivers of the mammal decline in northern Australia include inappropriate fi re regimes (too much fi re) and predation by feral cats. Cane Toads are also implicated, particularly to the recent catastrophic decline of the Northern Quoll. Furthermore, some impacts are due to vegetation changes associated with the pastoral industry. Disease could also be a factor, but to date there is little evidence for or against it. Based on current trends, many native mammals will become extinct in northern Australia in the next 10-20 years, and even the largest and most iconic national parks in northern Australia will lose native mammal species. This problem needs to be solved. The fi rst step towards a solution is to recognise the problem, and this publication seeks to alert the Australian community and decision makers to this urgent issue. -
Bara-Boodie.Pdf
ENGAGE E EXPLOR Bara EXPLAIN Boodie, the burrowing bettong ELABORATE E EVALUAT By Alwyn Evans Illustrated by Paul Ricketts ENDICES P AP PAGE 7 PART 1: LEARNING THROUGH STORY / BARA BOODIE, THE BURROWING BETTONG ENGAGE EXPLORE EXPLAIN ELABORATE long, long time ago, boodies lived contentedly all over Australia, in all A sorts of places: from shady woodlands with grasses and shrubs, to wide sandy deserts. EVALUAT Actually my friend, they lived in almost any place they fancied. Bara Boodie and her family’s home was the Australian Western Desert, in E Martu people’s country. They lived in a large cosy nest under a quandong tree, with many friends and neighbours nearby. Actually my friend, boodies loved to make friends with everyone. AP P Bara Boodie, the burrowing bettong ENDICES PART 1: LEARNING THROUGH STORY / BARA BOODIE, THE BURROWING BETTONG PAGE 8 ENGAGE o make their nests snug, Bara’s dad, mum and aunties collected bundles T of spinifex and grasses. Scampering on all fours, they carried their bundles with their fat, prehensile tails, back to their nests. E Actually my friend, they used any soft EXPLOR things they found. As they were small animals, all the family fitted cosily into their nest. Bara was only about 28 centimetres long, and her two brothers weren’t much more. Her mother and aunties were shorter than her father who was 40 centimetres long. At night they slept, curled EXPLAIN up together, with their short-muzzled faces and small rounded ears tucked into their fur. Actually my friend, they looked like one great big, grey, furry ball. -
Mixing Genetically and Morphologically Distinct
Article Mixing Genetically and Morphologically Distinct Populations in Translocations: Asymmetrical Introgression in A Newly Established Population of the Boodie (Bettongia lesueur) Rujiporn Thavornkanlapachai 1,*, Harriet R. Mills 2, Kym Ottewell 3, Judy Dunlop 4,5, Colleen Sims 5, Keith Morris 5, Felicity Donaldson 6 and W. Jason Kennington 1 1 School of Biological Sciences, The University of Western Australia, Crawley, Western Australia 6009, Australia; [email protected] 2 Centre for Ecosystem Management, School of Science, Edith Cowan University, Joondalup, Western Australia 6027, Australia; [email protected] 3 Department of Biodiversity, Conservation and Attractions, Locked Bag 104, Bentley Delivery Centre, Western Australia 6152, Australia; [email protected] 4 School of Veterinary and Biomedical Sciences, Murdoch University, Murdoch, Western Australia 6150, Australia; [email protected] 5 Department of Biodiversity, Conservation and Attractions, PO Box 51, Wanneroo, Western Australia 6946, Australia [email protected] (C.S.); [email protected] (K.M.) 6 360 Environmental, 10 Bermondsey Street, West Leederville, Western Australia 6007, Australia; [email protected] * Correspondence: [email protected]; Tel.: +61 8 9219 9089 Received: 22 August 2019; Accepted: 17 September 2019; Published: 19 September 2019 Abstract: The use of multiple source populations provides a way to maximise genetic variation and reduce the impacts of inbreeding depression in newly established translocated populations. However, there is a risk that individuals from different source populations will not interbreed, leading to population structure and smaller effective population sizes than expected. Here, we investigate the genetic consequences of mixing two isolated, morphologically distinct island populations of boodies (Bettongia lesueur) in a translocation to mainland Australia over three generations. -
Remotely Monitoring Change in Vegetation Cover on the Montebello Islands, Western Australia, in Response to Introduced Rodent Eradication
RESEARCH ARTICLE Remotely Monitoring Change in Vegetation Cover on the Montebello Islands, Western Australia, in Response to Introduced Rodent Eradication Cheryl Lohr1*, Ricky Van Dongen2, Bart Huntley2, Lesley Gibson3, Keith Morris1 1. Department of Parks and Wildlife, Science and Conservation Division, Woodvale, Western Australia, Australia, 2. Department of Parks and Wildlife, GIS Section, Kensington, Western Australia, Australia, 3. Department of Parks and Wildlife, Science and Conservation Division, Keiran McNamara Conservation Science Centre, 17 Dick Perry Drive, Technology Park, Kensington, WA 6151, Australia *[email protected] OPEN ACCESS Citation: Lohr C, Van Dongen R, Huntley B, Gibson L, Morris K (2014) Remotely Monitoring Abstract Change in Vegetation Cover on the Montebello Islands, Western Australia, in Response to The Montebello archipelago consists of 218 islands; 80 km from the north-west Introduced Rodent Eradication. PLoS ONE 9(12): e114095. doi:10.1371/journal.pone.0114095 coast of Western Australia. Before 1912 the islands had a diverse terrestrial fauna. Editor: Benjamin Lee Allen, University of By 1952 several species were locally extinct. Between 1996 and 2011 rodents and Queensland, Australia cats were eradicated, and 5 mammal and 2 bird species were translocated to the Received: September 16, 2014 islands. Monitoring of the broader terrestrial ecosystem over time has been limited. Accepted: October 29, 2014 We used 20 dry-season Landsat images from 1988 to 2013 and estimation of green Published: December 1, 2014 fraction cover in nadir photographs taken at 27 sites within the Montebello islands Copyright: ß 2014 Lohr et al. This is an open- and six sites on Thevenard Island to assess change in vegetation density over time. -
Woylie Or Brush-Tailed Bettong
Woylie Bettongia penicillata ogilbyi Conservation Status: Critically Endangered Identification The brush-tailed bettong Bettongia penicillata is a small kangaroo-like marsupial that was once found throughout much of mainland Australia. The subspecies Bettongia penicillata penicillata, endemic to south-eastern Australia, is considered extinct. Bettongia penicillata ogilbyi, commonly known as the woylie, is the only surviving subspecies and is found in the south- west of Western Australia. Photos: M. Bundock (left); R. McLean (right) Woylies have yellowish grey to reddish brown fur with a pale belly and a long, prehensile tail with a black brush at the end. They have strongly clawed forefeet, used for digging for food and nest making. They move about using all four legs and sometimes also their tail when foraging, but when flushed, they will bound extremely fast on their back legs with the head held low, back arched and tail almost straight. Head and body length: 280-365mm Tail length: 250-360mm Weight: 745-1850g Taxonomy Family: Potoroidae Genus: Bettongia Species: penicillata Subspecies: ogilbyi Other common names: brush-tailed bettong, brush-tailed rat-kangaroo Distribution and Habitat Brush-tailed bettongs were found across most of southern and central Australia prior to European settlement and the introduction of feral cats and foxes. The woylie is endemic to the south-west of WA but they are now only known from two areas: Upper Warren and Dryandra Woodlands. There are also translocated populations at Batalling, and inside fenced areas in Mt Gibson, Karakamia and Whiteman Park and also in New South Wales and South Australia, and on islands in SA.