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Greater Bilby Macrotis Lagotis
Threatened Species Strategy – Year 3 Priority Species Scorecard (2018) Greater Bilby Macrotis lagotis Key Findings Greater Bilbies once ranged over three‑ quarters of Australia, but declined coincident with the spread of European foxes, along with habitat changes from introduced herbivores (especially rabbits), changed fire regimes and predation by feral cats. Recovery actions have focused on maintaining or restoring traditional Indigenous patchwork fire regimes and controlling introduced predators. Translocations into predator-free exclosures and a predator-free island have allowed for further increases in population and re- establishment into the species’ former range. Photo: Queensland Department of Environment and Science Significant trajectory change from 2005-15 to 2015-18? No, generally stable overall. Priority future actions • Effective landscape-scale fire management is implemented across all of distribution. • Targeted cat and rabbit control at key bilby sites. • Minimise loss of bilby habitat, and maintain connectivity between bilby populations. Full assessment information Background information 2018 population trajectory assessment 1. Conservation status and taxonomy 8. Expert elicitation for population trends 2. Conservation history and prospects 9. Immediate priorities from 2019 3. Past and current trends 10. Contributors 4. Key threats 11. Legislative documents 5. Past and current management 12. References 6. Support from the Australian Government 13. Citation 7. Measuring progress towards conservation The primary purpose -
The Role of the Reintroduction of Greater Bilbies (Macrotis Lagotis)
The Role of the Reintroduction of Greater Bilbies (Macrotis lagotis) and Burrowing Bettongs (Bettongia lesueur) in the Ecological Restoration of an Arid Ecosystem: Foraging Diggings, Diet, and Soil Seed Banks Janet Newell School of Earth and Environmental Sciences University of Adelaide May 2008 A thesis submitted for the degree of Doctor of Philosophy Table of Contents ABSTRACT...............................................................................................................................................I DECLARATION.......................................................................................................................................III ACKNOWLEDGEMENTS ....................................................................................................................... V CHAPTER 1 INTRODUCTION ............................................................................................................1 1.1 MAMMALIAN EXTINCTIONS IN ARID AUSTRALIA ...............................................................................1 1.2 ROLE OF REINTRODUCTIONS .......................................................................................................2 1.3 ECOSYSTEM FUNCTIONS.............................................................................................................3 1.4 ECOSYSTEM FUNCTIONS OF BILBIES AND BETTONGS .....................................................................4 1.4.1 Consumers..........................................................................................................................4 -
Phylogenetic Relationships of Living and Recently Extinct Bandicoots Based on Nuclear and Mitochondrial DNA Sequences ⇑ M
Molecular Phylogenetics and Evolution 62 (2012) 97–108 Contents lists available at SciVerse ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Phylogenetic relationships of living and recently extinct bandicoots based on nuclear and mitochondrial DNA sequences ⇑ M. Westerman a, , B.P. Kear a,b, K. Aplin c, R.W. Meredith d, C. Emerling d, M.S. Springer d a Genetics Department, LaTrobe University, Bundoora, Victoria 3086, Australia b Palaeobiology Programme, Department of Earth Sciences, Uppsala University, Villavägen 16, SE-752 36 Uppsala, Sweden c Australian National Wildlife Collection, CSIRO Sustainable Ecosystems, Canberra, ACT 2601, Australia d Department of Biology, University of California, Riverside, CA 92521, USA article info abstract Article history: Bandicoots (Peramelemorphia) are a major order of australidelphian marsupials, which despite a fossil Received 4 November 2010 record spanning at least the past 25 million years and a pandemic Australasian range, remain poorly Revised 6 September 2011 understood in terms of their evolutionary relationships. Many living peramelemorphians are critically Accepted 12 September 2011 endangered, making this group an important focus for biological and conservation research. To establish Available online 11 November 2011 a phylogenetic framework for the group, we compiled a concatenated alignment of nuclear and mito- chondrial DNA sequences, comprising representatives of most living and recently extinct species. Our Keywords: analysis confirmed the currently recognised deep split between Macrotis (Thylacomyidae), Chaeropus Marsupial (Chaeropodidae) and all other living bandicoots (Peramelidae). The mainly New Guinean rainforest per- Bandicoot Peramelemorphia amelids were returned as the sister clade of Australian dry-country species. The wholly New Guinean Per- Phylogeny oryctinae was sister to Echymiperinae. -
The Collapse of Northern Mammal Populations 2 Australian
australian wildlife matters wildlife conservancy Winter 2010 The collapse of northern mammal populations 2 australian saving australia’s threatened wildlife wildlife Pictograph conservancy Welcome to our Winter 2010 edition of Wildlife Matters. I am writing this editorial from our bushcamp at Pungalina-Seven Emu, in the Gulf of Carpentaria. Our biological survey has just commenced and already some exciting discoveries have been made. the awc mission Overnight our fi eld ecologists captured a Carpentarian Pseudantechinus, one of Australia’s rarest mammals. This is only the 21st time that this species has ever been The mission of Australian Wildlife Conservancy recorded (the 20th record was also on Pungalina – see the Spring 2009 edition of (AWC) is the effective conservation of all Wildlife Matters). We have watched rare Ghost Bats, Australia’s only carnivorous bats, Australian animal species and the habitats in emerging from a maternity cave; a mother Dugong, with her calf, resting in the lower which they live. To achieve this mission, our reaches of the Calvert River; Bandicoots digging around Pungalina’s network of lush, actions are focused on: permanent springs; and graceful Antilopine Wallaroos bounding across Pungalina’s • Establishing a network of sanctuaries tropical savannas. which protect threatened wildlife and Pungalina-Seven Emu is a property of immense conservation signifi cance. Yet it ecosystems: AWC now manages lies at the centre – geographically – of an unfolding ecological drama which surely 21 sanctuaries covering over 2.5 million demands our attention: from Cape York to the Kimberley, Australia’s small mammals hectares (6.2 million acres). are disappearing. Species such as the Golden Bandicoot, the Brush-tailed Rabbit-rat • Implementing practical, on-ground and the Northern Quoll have suffered catastrophic declines, disappearing from large conservation programs to protect areas including places as famous and well resourced as Kakadu National Park. -
CITES Cop16 Prop. 9 IUCN-TRAFFIC Analysis (PDF, 77KB)
Ref. CoP16 Prop. 9 Deletion of Lesser Bilby Macrotis leucura from Appendix I Proponent: Australia Summary: The Lesser Bilby Macrotis leucura was one of two species of bilby (genus Macrotis) in the bandicoot family (the Peramelidae). It was endemic to Australia where it occurred in arid regions in the interior. The last verified specimen was collected in 1931, although oral accounts by Aboriginals suggest that it may have survived into the 1960s. It has been classified as Extinct by IUCN since 1982. The reasons for its demise are unclear, although predation by introduced Red Foxes Vulpes vulpes and feral cats and habitat alteration have been implicated. Macrotis leucura, along with its sister-species the Greater Bilby Macrotis lagotis, was included in CITES Appendix I in 1975, when the Convention came into force, by which time it was almost certainly extinct. No trade in any specimens has ever been recorded under CITES. In the highly unlikely event of the species being rediscovered, it would be covered by Australian legislation that prohibits the export of native mammal species for commercial purposes and requires a permit for export for non-commercial purposes. Macrotis lagotis, which is easily distinguishable from M. leucura by its greater size and different colouration, is extant and classified as Vulnerable by IUCN. A very small amount of non-commercial trade in specimens of this species is recorded in the CITES trade database. Analysis: Resolution Conf. 9.24 (Rev. CoP15) notes in Annex 4 (Precautionary measures) that no species listed in Appendix I shall be removed from the Appendices unless it has been first transferred to Appendix II, with monitoring of any impact of trade on the species for at least two intervals between meetings of the Conference of the Parties (para. -
Thylacomyidae
FAUNA of AUSTRALIA 25. THYLACOMYIDAE KEN A. JOHNSON 1 Bilby–Macrotis lagotis [F. Knight/ANPWS] 25. THYLACOMYIDAE DEFINITION AND GENERAL DESCRIPTION The family Thylacomyidae is a distinctive member of the bandicoot superfamily Perameloidea and is represented by two species, the Greater Bilby, Macrotis lagotis, and the Lesser Bilby, M. leucura. The Greater Bilby is separated from the Lesser Bilby by its greater size: head and body length 290–550 mm versus 200–270 mm; tail 200–290 mm versus 120–170 mm; and weight 600–2500 g versus 311–435 g respectively (see Table 25.1). The dorsal pelage of the Greater Bilby is blue-grey with two variably developed fawn hip stripes. The tail is black around the full circumference of the proximal third, contrasting conspicuously with the pure white distal portion, which has an increasingly long dorsal crest. The Lesser Bilby displays a delicate greyish tan above, described by Spencer (1896c) as fawn-grey and lacks the pure black proximal portion in the tail. Rather, as its specific name implies, the tail is white throughout, although a narrow band of slate to black hairs is present on the proximal third of the length. Finlayson (1935a) noted that the Greater Bilby lacks the strong smell of the Lesser Bilby. The skull of the Lesser Bilby is distinguished from the Greater Bilby by its smaller size (basal length 60-66 mm versus 73–104 mm; [Troughton 1932; Finlayson 1935a]), the more inflated and smoother tympanic bullae (Spencer 1896c), the absence of a fused sagittal crest in old males and the distinctly more cuspidate character in the crowns in the unworn molars (Finlayson 1935a). -
Wildlife Matters Wildlife Conservancy
australian wildlife matters wildlife conservancy Spring 2009 Pungalina reveals one of Australia’s rarest mammals Carpentarian Pseudantechinus 2 australian saving australia’s threatened wildlife wildlife Pictograph conservancy Welcome to the Spring 2009 edition of Wildlife Matters. As this edition goes to print, we are in the process of fi nalising the acquisition of Bowra (see pages 4-5), a 14,000 the awc mission hectare property located in the heart of the Mulga Lands in Queensland. Bowra will The mission of Australian Wildlife Conservancy be our 21st sanctuary, bringing the AWC network to more than 2.56 million hectares (AWC) is the effective conservation of all (6.3 million acres). Australian animal species and the habitats in While the overall scale of the portfolio is impressive, it is not the number of properties or which they live. To achieve this mission, our hectares that really count. A more accurate measure of the value of the portfolio is the actions are focused on: number of species and ecosystems that occur within the AWC estate. In this respect, • Establishing a network of sanctuaries the statistics are even more impressive – for example, around 80% of all Australian which protect threatened wildlife and terrestrial bird species and over 60% of all terrestrial mammal species occur on one or ecosystems: AWC now manages 20 more of our sanctuaries. sanctuaries covering over 2.56 million The fact that our portfolio captures such a high percentage of Australia’s wildlife species hectares (6.3 million acres). refl ects a deliberate, science-based strategy to ensure that AWC invests in properties • Implementing practical, on-ground of the highest environmental value. -
Verifying Bilby Presence and the Systematic
CSIRO PUBLISHING Australian Mammalogy Review https://doi.org/10.1071/AM17028 Verifying bilby presence and the systematic sampling of wild populations using sign-based protocols – with notes on aerial and ground survey techniques and asserting absence Richard Southgate A, Martin A. Dziminski B,E, Rachel Paltridge C, Andrew Schubert C and Glen Gaikhorst D AEnvisage Environmental Services, PO Box 305, Kingscote, SA 5223, Australia. BDepartment of Biodiversity, Conservation and Attractions, Western Australia, Woodvale Wildlife Research Centre, Locked Bag 104, Bentley Delivery Centre, WA 6983, Australia. CDesert Wildlife Services, PO Box 4002, Alice Springs, NT 0871, Australia. DGHD Pty Ltd, 999 Hay Street, Perth, WA 6004, Australia. ECorresponding author. Email: [email protected] Abstract. The recognition of sign such as tracks, scats, diggings or burrows is widely used to detect rare or elusive species. We describe the type of sign that can be used to confirm the presence of the greater bilby (Macrotis lagotis)in comparison with sign that should be used only to flag potential presence. Clear track imprints of the front and hind feet, diggings at the base of plants to extract root-dwelling larvae, and scats commonly found at diggings can be used individually, or in combination, to verify presence, whereas track gait pattern, diggings in the open, and burrows should be used to flag potential bilby activity but not to verify presence. A protocol to assess potential activity and verify bilby presence is provided. We provide advice on the application of a plot-based technique to systematically search for sign and produce data for the estimation of regional occupancy. -
Bandicoot Fossils and DNA Elucidate Lineage Antiquity Amongst Xeric
www.nature.com/scientificreports OPEN Bandicoot fossils and DNA elucidate lineage antiquity amongst xeric-adapted Received: 31 May 2016 Accepted: 31 October 2016 Australasian marsupials Published: 24 November 2016 Benjamin P. Kear1,2, Ken P. Aplin3 & Michael Westerman4 Bandicoots (Peramelemorphia) are a unique order of Australasian marsupials whose sparse fossil record has been used as prima facie evidence for climate change coincident faunal turnover. In particular, the hypothesized replacement of ancient rainforest-dwelling extinct lineages by antecedents of xeric-tolerant extant taxa during the late Miocene (~10 Ma) has been advocated as a broader pattern evident amongst other marsupial clades. Problematically, however, this is in persistent conflict with DNA phylogenies. We therefore determine the pattern and timing of bandicoot evolution using the first combined morphological + DNA sequence dataset of Peramelemorphia. In addition, we document a remarkably archaic new fossil peramelemorphian taxon that inhabited a latest Quaternary mosaic savannah-riparian forest ecosystem on the Aru Islands of Eastern Indonesia. Our phylogenetic analyses reveal that unsuspected dental homoplasy and the detrimental effects of missing data collectively obscure stem bandicoot relationships. Nevertheless, recalibrated molecular clocks and multiple ancestral area optimizations unanimously infer an early diversification of modern xeric-adapted forms. These probably originated during the late Palaeogene (30–40 Ma) alongside progenitors of other desert marsupials, and thus occupied seasonally dry heterogenous habitats long before the onset of late Neogene aridity. Bandicoots (Peramelemorphia) are a speciose order of Australasian marsupials that appeared early in the evolu- tionary history of Australidelphia1. Most are small to medium sized (up to 5 kg) terrestrial omnivores occupying a spectrum of rainforest to desert habitats2,3. -
Discovering Marsupials Snout, and Enlarged Front Legs
Discovered by Mark Harvey, Western Australian Museum ustralia, New Guinea and some They delved deeper into nearby islands are home to the the status of the quenda, which Avast majority of living marsupials, is endemic to south-western a group of mammals that separated from Australia. It has usually been other mammals in the Mesozoic, about considered as a subspecies 160 million years ago. Elsewhere, marsupials known as Isoodon obesulus are only known from the Americas, although fusciventer, with the other fossils have been found in Asia and Europe. subspecies found in south- Many Australian marsupials have become eastern Australia. However, iconic and are much-loved symbols of Kenny and Matthew raised our nation. Sadly, many are imperilled by it to a full species, finding land clearing and threats from introduced consistent differences in predators. the shape of some of the One of the most distinctive (and teeth and some previously perhaps cute) marsupial groups comprises published molecular data. the bandicoots and bilbies which This species is now known as are classified in their own order, the Isoodon fusciventer. Peramelemorphia. They have long ears and They then turned their Discovering marsupials snout, and enlarged front legs. There are attention to the other only about 22 living species of bandicoots genus, Perameles. Previous and they are only found in the Australo- classifications recognised only Papuan region. Their size and relatively a few modern species, including the long- Above A western barred bandicoot. placid nature has made them vulnerable nosed bandicoot (P. nasuta) from eastern Photo – Jiri Lochman to land-clearing and introduced predators Australia, the eastern barred bandicoot such as feral cats and foxes, and many (P. -
Greater Bilby Macrotis Lagotis
Endangered Greater Bilby Macrotis lagotis Greater Bilbies are culturally important marsupials about the size of small cats. They are the largest member of the bandicoot family – adult females weigh about 1 kg and males are twice that weight. They have long, highly sensitive ears that are important for keeping them cool and hearing predators. This, and their long, silky fur and white tipped tails, make it easy to tell them apart from other bandicoots. Greater Bilbies have Bioregion resources strong front limbs like a kangaroo. They also have poor vision but good senses of hearing and smell. Greater Bilbies were presumed extinct in South Australia in the 1930s. Indigenous names for the Greater Bilby include Ninu (Pitjantjatjara), Walpajirri (Warlpiri), Ahert (Arrente) and Mankarr (Manjilyjarra). Diet Greater Bilbies forage at night, travelling up to five km to find food. They are omnivorous and feed on invertebrates (e.g. termites, witchetty grubs and spiders) fungi, seeds, bulbs and occasionally, small vertebrates they dig up. Breeding Most of the time, Greater Bilbies live alone, but they may live in family groups of two to four when they have young. Breeding is possible all year round but usually depends on rainfall and the availability of food. Female bilbies give birth to one to three young, which stay in the pouch for about 2.5 months (a Bilby’s pouch contains eight teats). Habitat Greater Bilbies were once common across 70 per cent of the Australian mainland but now their distribution has been greatly reduced. They live in sandy deserts, inside burrows that spiral down to around two metres deep. -
GREATER BILBY BILBY Macrotis Lagotis
Threatened Species of the Northern Territory GREATER BILBY BILBY Macrotis lagotis Conservation status Australia: Vulnerable Northern Territory: Vulnerable Description Historically, the greater bilby occupied a vast area of arid and semi-arid Australia. Its The greater bilby is a large bandicoot (body distribution declined dramatically in the years mass males, 800-2500g; females, 600-1100g) following European settlement and it now with soft silky fur. The fur is ash grey over occupies about 20% of its former range. The most of the body, whereas on the belly it is species occurs in two separate geographic pure white to cream. The basal 20 percent of areas; one extending from the western the tail is the same colour as the upper-body, deserts region of the Northern Territory and the central 40 percent is black and the distal Western Australia north to the Pilbara and 40 percent, pure white. The forelimbs are Kimberley regions, the second in the Channel robust and equipped with three stoutly Country of south-west Queensland (Watts clawed toes (and two unclawed toes) giving 1969; Southgate 1990a). the animal a formidable burrowing capacity. The slender hind limbs are long and resemble those of macropods. The snout is long and delicate and the ears are large and rabbit-like. Distribution Within the Northern Territory, it occurs in the central and western parts of the Tanami bioregion, the southern Sturt Plateau bioregion and the northern Great Sandy Desert bioregion. The distribution is highly fragmented within this area. The most southerly recent records are in the vicinity of Kintore, the most northerly around Newcastle Waters and Wave Hill.