Listing Advice Mesembriomys Macrurus Golden-Backed Tree-Rat

Total Page:16

File Type:pdf, Size:1020Kb

Listing Advice Mesembriomys Macrurus Golden-Backed Tree-Rat THREATENED SPECIES SCIENTIFIC COMMITTEE Established under the Environment Protection and Biodiversity Conservation Act 1999 The Minister deleted this species from the Vulnerable category effective from 22 Feburary 2019 Listing Advice Mesembriomys macrurus Golden-backed Tree-rat Taxonomy Conventionally accepted as Mesembriomys macrurus (Peters, 1876). No subspecies are recognised. Summary of assessment Conservation status The Golden-backed Tree-rat was listed as Vulnerable effective July 2000. The assessment has determined that the species is no longer eligible for inclusion in any category of the list and is eligible for delisting. Species can be listed as threatened under state and territory legislation. For information on the listing status of this species under relevant state or territory legislation, see http://www.environment.gov.au/cgi-bin/sprat/public/sprat.pl Reason for conservation assessment by the Threatened Species Scientific Committee The Golden-backed Tree-rat was listed as Vulnerable under the predecessor to the Environmental Protection and Biodiversity Conservation Act 1999 (EPBC Act) the Endangered Species Protection Act 1992 and transferred to the EPBC Act in July 2000. This advice follows assessment of new information provided to the Committee to change the listing status of the Golden-backed Tree-rat. Public Consultation Notice of the proposed amendment and a consultation document was made available for public comment for 30 business days between 20 April 2018 and 1 June 2018. Any comments received that were relevant to the survival of the species were considered by the Committee as part of the assessment process. Species information Description The Golden-backed Tree-rat is a large rodent weighing 207−330 g, with a head and body length of 188−245 mm and a tail length of 291−360 mm (McKenzie & Kerle 2008). It is midway in size between two other large semi-arboreal species in northern Australia, the smaller Conilurus penicillatus (Brush-tailed Rabbit-rat) and the larger Mesembriomys gouldii (Black-footed Tree-rat). Its fur is grey above and on the sides, and creamy white below. The feet are white. The basal third of the long tail is grey while the remainder is white; the terminal third has a white brush. A distinctive mid-dorsal stripe of orange-brown fur, which stretches along the back of the crown to the base of the tail, distinguishes it from all other tree-rats (McKenzie & Kerle 2008). Mesembriomys macrurus (Golden-backed Tree-rat) Listing Advice Page 1 of 17 Indigenous names include Koorrawal, Wunggangbarn or Jari (Jaradada et al. 2011) and Jarri Manya (Cheinmora et al. 2017). Distribution The Golden-backed Tree-rat has been recorded from the top end of the Northern Territory (NT), and the Kimberley and Pilbara in Western Australia (WA). It has undergone a substantial historical range contraction and appears to have disappeared from the NT, the Pilbara and the south-west Kimberley (Palmer et al. 2003). Historical In the Northern Territory it has been recorded at three sites: ‘Balanbrinni’ (probably Balbarini) in the upper McArthur in 1901; Nellie Creek (in the upper Mary River) in 1903; and Deaf Adder Gorge in 1969 (Parker 1973). It has not been confirmed anywhere else in the Northern Territory despite many surveys across much of the Top End of the Northern Territory over the last 40 years (Woinarski et al. 2012). A review of Indigenous knowledge across the Top End has suggested that the final phase of its decline in the NT was very recent, with plausible records between the late 2000s and early 2010s (Ziembicki et al. 2013). However, there is a small possibility that it may still exist in the Northern Territory, as surveys have not been extensive or intensive, and the species is difficult to detect as it occurs in thick and complex habitat in remote and difficult to access areas (DENR 2018. pers comm 3 May). In Western Australia, subfossil records from Cape Range show that it once had a Pilbara distribution (Baynes & McDowell 2011), with the type specimen originating from near Roebourne in 1875 (McKenzie & Kerle 2008). However, since 1903 all known records have come from the higher rainfall areas of the north-west Kimberley, and the species has disappeared from the Pilbara (McKenzie & Kerle 2008) and drier parts of the Kimberley (McKenzie 1981a). Current The current distribution of the Golden-backed Tree-rat is restricted to the north-west Kimberley (Start et al. 2012), from near Kalumburu in the north to Yampi Peninsula in the south (e.g. Kitchener et al. 1981), including several Kimberley islands in the Buccaneer Archipelago (DPaW 2012). The species occurs in the Mitchell Plateau, Prince Regent National Park, Artesian Range and Yampi Peninsula. It has also been recorded more recently from a number of locations in pockets of suitable gorge country in the King Leopold Ranges, more than 100 km inland in the central Kimberley (I Radford, unpublished data; Corey & Radford 2017). It has been recorded on 11 islands: Augustus, Carlia, Chambers, Conilurus, Hidden, Jar, Lachlan, an unnamed island in Scott Strait, Uwins, Wollaston and Buckle Head (Burbidge & Abbott 2017; Legge et al. 2018; A Burbidge 2018. pers comm 1 August). Prince Regent National Park (including part of Bachsten Creek) is managed by the WA Department of Biodiversity, Conservation and Attractions. The remaining land on which the species occurs is largely managed by Indigenous peoples: • Mitchell River National Park and Lawley River National Park − native title areas managed by the Wunambal Gaambera Aboriginal Corporation (WGAC); • Uunguu Indigenous Protected Area (IPA), Mitchell Plateau – on the national reserve system, managed by WGAC; • Wilinggin IPA, including part of Bachsten Creek (e.g. Bachsten Camp) – managed by the Wilinggin Aboriginal Corporation (WAC); • Dambimangari IPA − on the national reserve system, managed by the Dambimangari Aboriginal Corporation (DAC); • Kimberley Islands – part of the IPAs or native title management by Mayala, Dambimangari and Uunguu; Mesembriomys macrurus (Golden-backed Tree-rat) Listing Advice Page 2 of 17 • Charnley River station, including part of the Artesian Range (Charnley-Artesian Range Wildlife Sanctuary) – a pastoral lease managed by the Australian Wildlife Conservancy (AWC), with native title interests (WAC); • Yampi Sound Training Area – Australian Government Defence Land and Aboriginal Reserve. The AWC has an agreement with the Department of Defence and a partnership with DAC to manage the land. (T Vigilante 2018. pers comm 24 April & 3 August; AWC 2018. pers comm 31 May; K Mitchell 2018. pers comm 3 August). Cultural significance The tails of the Golden-backed Tree-rat were traditionally used to make special necklaces by the Indigenous people of Wunambal Gaambera Country in the north-west Kimberley (Karadada et al. 2011, p. 98). Relevant biology/ecology In its current range the Golden-backed Tree-rat occurs in a variety of highland and lowland habitats, including rainforest and riparian areas (on volcanic, lateritic, sandstone and floodplain surfaces), eucalypt-dominated woodlands and savannas (particularly with fruiting trees and shrubs), Livistona palm woodlands, and rugged sandstone plateaux and screes (Woinarski et al. 2014; AWC 2018. pers comm 31 May). Other geological associations include rolling quartzite hills, granite hills, and lowland plains adjacent to hills and escarpments (AWC 2018. pers comm 31 May). In savannas it is more abundant in high rainfall rocky areas (Radford et al. 2014). The species is largely nocturnal, but individuals have been seen foraging shortly before dusk and soon after sunrise (Woinarski et al. 2014; Hohnen et al. 2015). In thick vegetation and near vertical rock faces, it is mainly arboreal (on trees or rocks) but spends time on the ground. The species can quickly move long distances, often through dense grass, scampering along with its tail held high. In sparser vegetation and rocky areas, it spends most of its time on the ground (Woinarski et al. 2014). The Indigenous Kwini people of the far-north Kimberley observed that it “[ran] around trees and hunt[ed] on the ground” (Cheinmora et al. 2017, p. 170). It has been observed denning in tree hollows, in rock scree, and on cliffs, or occasionally in loose woven nests under the spiky crown of pandanus (McKenzie & Kerle 2008; Hohnen et al. 2015). The species utilises the edge of rainforest patches for foraging, feeding in both the rainforest and adjacent eucalypt woodland (Woinarski et al. 2014). The home ranges of animals in the Artesian Range are on average 6.3 ha, varying between 0.24 and 30.44 ha (Hohnen et al. 2015). Individuals are known to travel over 1 km from their refuge into open savanna to forage at night (Hohnen et al. 2015). Flowers, fruits and termites have been recorded as the main dry- season foods, but grasses, ants and beetles are occasionally eaten (Morton 1991). Pregnant females and juveniles have been recorded in August, October and November, suggesting a mid- to late- dry season breeding period. The litter size is usually two, but one and three have been recorded (McKenzie & Kerle 2008). Longevity in captivity is 7 years (Weigl 1971, in AnAge 2012). Generation time is here assumed to be around 3 years. In the wet-dry tropics, climatic variability (particularly rainfall), through its influence on food supply, may strongly influence demographic changes in populations and give rise to opportunistic breeding in some species (Bolton et al. 1982, Kerle & Burgman 1984, Friend 1987a). Populations of the Black-footed Tree-rat in the wet-dry tropics of the Northern Territory markedly increased in size following a high rainfall event in 1981, and declined following lack of rain in 1983 (Taylor & Tullock 1985; Friend 1987b). However, in an analysis of data from eight mammal surveys from 1994 to 2011, Radford et al. (2014) found no evidence of order of magnitude changes in the abundance of mammal species (including the Golden-backed Tree- rat) in tropical savannas of the Kimberley due to annual changes in rainfall.
Recommended publications
  • Calaby References
    Abbott, I.J. (1974). Natural history of Curtis Island, Bass Strait. 5. Birds, with some notes on mammal trapping. Papers and Proceedings of the Royal Society of Tasmania 107: 171–74. General; Rodents; Abbott, I. (1978). Seabird islands No. 56 Michaelmas Island, King George Sound, Western Australia. Corella 2: 26–27. (Records rabbit and Rattus fuscipes). General; Rodents; Lagomorphs; Abbott, I. (1981). Seabird Islands No. 106 Mondrain Island, Archipelago of the Recherche, Western Australia. Corella 5: 60–61. (Records bush-rat and rock-wallaby). General; Rodents; Abbott, I. and Watson, J.R. (1978). The soils, flora, vegetation and vertebrate fauna of Chatham Island, Western Australia. Journal of the Royal Society of Western Australia 60: 65–70. (Only mammal is Rattus fuscipes). General; Rodents; Adams, D.B. (1980). Motivational systems of agonistic behaviour in muroid rodents: a comparative review and neural model. Aggressive Behavior 6: 295–346. Rodents; Ahern, L.D., Brown, P.R., Robertson, P. and Seebeck, J.H. (1985). Application of a taxon priority system to some Victorian vertebrate fauna. Fisheries and Wildlife Service, Victoria, Arthur Rylah Institute of Environmental Research Technical Report No. 32: 1–48. General; Marsupials; Bats; Rodents; Whales; Land Carnivores; Aitken, P. (1968). Observations on Notomys fuscus (Wood Jones) (Muridae-Pseudomyinae) with notes on a new synonym. South Australian Naturalist 43: 37–45. Rodents; Aitken, P.F. (1969). The mammals of the Flinders Ranges. Pp. 255–356 in Corbett, D.W.P. (ed.) The natural history of the Flinders Ranges. Libraries Board of South Australia : Adelaide. (Gives descriptions and notes on the echidna, marsupials, murids, and bats recorded for the Flinders Ranges; also deals with the introduced mammals, including the dingo).
    [Show full text]
  • Quaternary Murid Rodents of Timor Part I: New Material of Coryphomys Buehleri Schaub, 1937, and Description of a Second Species of the Genus
    QUATERNARY MURID RODENTS OF TIMOR PART I: NEW MATERIAL OF CORYPHOMYS BUEHLERI SCHAUB, 1937, AND DESCRIPTION OF A SECOND SPECIES OF THE GENUS K. P. APLIN Australian National Wildlife Collection, CSIRO Division of Sustainable Ecosystems, Canberra and Division of Vertebrate Zoology (Mammalogy) American Museum of Natural History ([email protected]) K. M. HELGEN Department of Vertebrate Zoology National Museum of Natural History Smithsonian Institution, Washington and Division of Vertebrate Zoology (Mammalogy) American Museum of Natural History ([email protected]) BULLETIN OF THE AMERICAN MUSEUM OF NATURAL HISTORY Number 341, 80 pp., 21 figures, 4 tables Issued July 21, 2010 Copyright E American Museum of Natural History 2010 ISSN 0003-0090 CONTENTS Abstract.......................................................... 3 Introduction . ...................................................... 3 The environmental context ........................................... 5 Materialsandmethods.............................................. 7 Systematics....................................................... 11 Coryphomys Schaub, 1937 ........................................... 11 Coryphomys buehleri Schaub, 1937 . ................................... 12 Extended description of Coryphomys buehleri............................ 12 Coryphomys musseri, sp.nov.......................................... 25 Description.................................................... 26 Coryphomys, sp.indet.............................................. 34 Discussion . ....................................................
    [Show full text]
  • Natural History of the Eutheria
    FAUNA of AUSTRALIA 35. NATURAL HISTORY OF THE EUTHERIA P. J. JARMAN, A. K. LEE & L. S. HALL (with thanks for help to J.H. Calaby, G.M. McKay & M.M. Bryden) 1 35. NATURAL HISTORY OF THE EUTHERIA 2 35. NATURAL HISTORY OF THE EUTHERIA INTRODUCTION Unlike the Australian metatherian species which are all indigenous, terrestrial and non-flying, the eutherians now found in the continent are a mixture of indigenous and exotic species. Among the latter are some intentionally and some accidentally introduced species, and marine as well as terrestrial and flying as well as non-flying species are abundantly represented. All the habitats occupied by metatherians also are occupied by eutherians. Eutherians more than cover the metatherian weight range of 5 g–100 kg, but the largest terrestrial eutherians (which are introduced species) are an order of magnitude heavier than the largest extant metatherians. Before the arrival of dingoes 4000 years ago, however, none of the indigenous fully terrestrial eutherians weighed more than a kilogram, while most of the exotic species weigh more than that. The eutherians now represented in Australia are very diverse. They fall into major suites of species: Muridae; Chiroptera; marine mammals (whales, seals and dugong); introduced carnivores (Canidae and Felidae); introduced Leporidae (hares and rabbits); and introduced ungulates (Perissodactyla and Artiodactyla). In this chapter an attempt is made to compare and contrast the main features of the natural histories of these suites of species and, where appropriate, to comment on their resemblance to or difference from the metatherians. NATURAL HISTORY Ecology Diet. The native rodents are predominantly omnivorous.
    [Show full text]
  • 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.
    [Show full text]
  • 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.
    [Show full text]
  • Reintroducing the Dingo: the Risk of Dingo Predation to Threatened Vertebrates of Western New South Wales
    CSIRO PUBLISHING Wildlife Research http://dx.doi.org/10.1071/WR11128 Reintroducing the dingo: the risk of dingo predation to threatened vertebrates of western New South Wales B. L. Allen A,C and P. J. S. Fleming B AThe University of Queensland, School of Animal Studies, Gatton, Qld 4343, Australia. BVertebrate Pest Research Unit, NSW Department of Primary Industries, Orange Agricultural Institute, Forest Road, Orange, NSW 2800, Australia. CCorresponding author. Present address: Vertebrate Pest Research Unit, NSW Department of Primary Industries, Sulfide Street, Broken Hill, NSW 2880, Australia. Email: [email protected] Abstract Context. The reintroduction of dingoes into sheep-grazing areas south-east of the dingo barrier fence has been suggested as a mechanism to suppress fox and feral-cat impacts. Using the Western Division of New South Wales as a case study, Dickman et al. (2009) recently assessed the risk of fox and cat predation to extant threatened species and concluded that reintroducing dingoes into the area would have positive effects for most of the threatened vertebrates there, aiding their recovery through trophic cascade effects. However, they did not formally assess the risk of dingo predation to the same threatened species. Aims. To assess the risk of dingo predation to the extant and locally extinct threatened vertebrates of western New South Wales using methods amenable to comparison with Dickman et al. (2009). Methods. The predation-risk assessment method used in Dickman et al. (2009) for foxes and cats was applied here to dingoes, with minor modification to accommodate the dietary differences of dingoes. This method is based on six independent biological attributes, primarily reflective of potential vulnerability characteristics of the prey.
    [Show full text]
  • Rodents Bibliography
    Calaby’s Rodent Literature Abbott, I.J. (1974). Natural history of Curtis Island, Bass Strait. 5. Birds, with some notes on mammal trapping. Papers and Proceedings of the Royal Society of Tasmania 107: 171–74. General; Rodents Abbott, I. (1978). Seabird islands No. 56 Michaelmas Island, King George Sound, Western Australia. Corella 2: 26–27. (Records rabbit and Rattus fuscipes). General; Rodents; Lagomorphs Abbott, I. (1981). Seabird Islands No. 106 Mondrain Island, Archipelago of the Recherche, Western Australia. Corella 5: 60–61. (Records bush-rat and rock-wallaby). General; Rodents Abbott, I. and Watson, J.R. (1978). The soils, flora, vegetation and vertebrate fauna of Chatham Island, Western Australia. Journal of the Royal Society of Western Australia 60: 65–70. (Only mammal is Rattus fuscipes). General; Rodents Adams, D.B. (1980). Motivational systems of agonistic behaviour in muroid rodents: a comparative review and neural model. Aggressive Behavior 6: 295–346. Rodents Ahern, L.D., Brown, P.R., Robertson, P. and Seebeck, J.H. (1985). Application of a taxon priority system to some Victorian vertebrate fauna. Fisheries and Wildlife Service, Victoria, Arthur Rylah Institute of Environmental Research Technical Report No. 32: 1–48. General; Marsupials; Bats; Rodents; Whales; Land Carnivores Aitken, P. (1968). Observations on Notomys fuscus (Wood Jones) (Muridae-Pseudomyinae) with notes on a new synonym. South Australian Naturalist 43: 37–45. Rodents; Aitken, P.F. (1969). The mammals of the Flinders Ranges. Pp. 255–356 in Corbett, D.W.P. (ed.) The natural history of the Flinders Ranges. Libraries Board of South Australia : Adelaide. (Gives descriptions and notes on the echidna, marsupials, murids, and bats recorded for the Flinders Ranges; also deals with the introduced mammals, including the dingo).
    [Show full text]
  • Haematology and Serum Biochemistry in Captive Australian Native Murids: Black‑Footed Tree‑Rat (Mesembriomys Gouldii) and Greater Stick‑Nest Rat (Leporillus Conditor)
    Tulk et al. SpringerPlus (2016) 5:1479 DOI 10.1186/s40064-016-3111-7 RESEARCH Open Access Haematology and serum biochemistry in captive Australian native murids: black‑footed tree‑rat (Mesembriomys gouldii) and greater stick‑nest rat (Leporillus conditor) Melissa L. Tulk1, Hayley J. Stannard2 and Julie M. Old1* *Correspondence: [email protected] Abstract 1 School of Science The black-footed tree-rat (Mesembriomys gouldii) and greater stick-nest rat (Leporillus and Health, Hawkesbury, Western Sydney University, conditor) are near threatened and vulnerable native Australian murids. There is a pau- Locked Bag 1797, Penrith, city of health and welfare knowledge for these species and native murids in general. In NSW 2751, Australia this paper we aimed to address this deficiency in knowledge by describing some key Full list of author information is available at the end of the haematological and blood biochemistry parameters for these species. Haematology article and blood biochemistry data were obtained from clinical histories of the two murid species held in captivity at Taronga Zoological Park, Mosman, Australia. The data were analysed to establish confidence intervals for each parameter available and leukocyte morphology described. White blood cell counts were higher in females than males. Both species also had high neutrophil:lymphocyte ratios (tree-rat ratios were almost even). Haematocrit was higher in male stick-nest rats than females. Differential leuko- cyte counts and leukocyte morphology was consistent with previous descriptions in other murids and between individuals. Blood biochemistry values were unremarkable except for the high level of globulin in stick-nest rats. The values provided in the study will add to the knowledge of health data for murids in captivity and aid captive and natural management of Australian native murids.
    [Show full text]
  • Psmissen Phd Thesis
    Evolutionary biology of Australia’s rodents, the Pseudomys and Conilurus Species Groups Peter J. Smissen Submitted in total fulfilment of the requirements of the degree of DOCTOR OF PHILOSOPHY May 2017 School of BioSciences Faculty of Science University of Melbourne Produced on archival quality paper 1 Dedicated to my parents: Ian and Joanne Smissen. 2 Abstract The Australian rodents represent terminal expansions of the most diverse family of mammals in the world, Muridae. They colonised New Guinea from Asia twice and Australia from New Guinea several times. They have colonised all Australian terrestrial environments including deserts, forests, grasslands, and rivers from tropical to temperate latitudes and from sea level to highest peaks. Despite their ecological and evolutionary success Australian rodents have faced an exceptionally high rates of extinction with >15% of species lost historically and most others currently threatened with extinction. Approximately 50% of Australian rodents are recognised in the Pseudomys Division (Musser and Carleton, 2005), including 3 of 10 historically extinct species. The division is not monophyletic with the genera Conilurus, Mesembriomys, and Leporillus (hereafter Conilurus Species Group, CSG) more closely related to species of the Uromys division to the exclusion of Zyzomys, Leggadina, Notomys, Pseudomys and Mastacomys (hereafter Pseudomys Species Group, PSG). In this thesis, I resolved phylogenetic relationships and biome evolution among living species of the PSG, tested species boundaries in a phylogeographically-structured species, and incorporated extinct species into a phylogeny of the CSG. To resolve phylogenetic relationships within the Pseudomys Species Group (PSG) I used 10 nuclear loci and one mitochondrial locus from all but one of the 33 living species.
    [Show full text]
  • Ecology and Conservation Status of the Brush-Tailed Rabbit-Rat Conilurus Penicillatus
    Ecology and conservation status of the brush-tailed rabbit-rat Conilurus penicillatus Ronald Stuart Craig Firth B. Sc. (Hons) (Monash) Faculty of Education, Health and Science Charles Darwin University A thesis submitted to satisfy the requirements of a degree of Doctor of Philosophy (Science) ii Declaration I hereby declare that the work herein, submitted as a thesis for the degree of Doctor of Philosophy (Science) at Charles Darwin University is the result of my own investigations, and all references to ideas and work of other researchers have been specifically acknowledged. I hereby certify that the work embodied in this thesis has not already been accepted in substance for any degree, and is not being currently submitted in candidature for any other degree. Ronald Stuart Craig Firth / / iii Acknowledgements Firstly I would like to thank my supervisors John Woinarski and Richard Noske, in particular John Woinarski for envisaging the project but first and foremost for his outstanding intellectual input for which I could not have done without and of course for also editing many drafts; Richard Noske for his help with all the administrative goings on associated with a PhD, for editing drafts and the occasional tasty cake. Charles Darwin University provided me with a scholarship and some project funding. Additional funding to conduct the research was also provided by the CRC for Tropical Savannas Management, the Biodiversity Conservation Division, Department of Natural Resources Environment and the Arts and Australian Geographic. Many
    [Show full text]
  • Decline and Extinction of Australian Mammals Since European Settlement
    Ongoing unraveling of a continental fauna: Decline FEATURE ARTICLE and extinction of Australian mammals since European settlement John C. Z. Woinarskia,b,1, Andrew A. Burbidgec, and Peter L. Harrisond aNorthern Australian Hub of National Environmental Research Program and bThreatened Species Recovery Hub of National Environmental Science Program, SEE COMMENTARY Charles Darwin University, Darwin, NT 0909, Australia; cResearch Fellow, Department of Parks and Wildlife, Wanneroo, WA 6069, Australia; and dMarine Ecology Research Centre, School of Environment, Science and Engineering, Southern Cross University, Lismore, NSW 2480, Australia This Feature Article is part of a series identified by the Editorial Board as reporting findings of exceptional significance. Edited by William J. Bond, University of Cape Town, Cape Town, South Africa, and approved January 13, 2015 (received for review September 10, 2014) The highly distinctive and mostly endemic Australian land mam- than previously recognized and that many surviving Australian mal fauna has suffered an extraordinary rate of extinction (>10% native mammal species are in rapid decline, notwithstanding the of the 273 endemic terrestrial species) over the last ∼200 y: in generally low level in Australia of most of the threats that are comparison, only one native land mammal from continental North typically driving biodiversity decline elsewhere in the world. America became extinct since European settlement. A further 21% of Australian endemic land mammal species are now assessed to Earlier Losses be threatened, indicating that the rate of loss (of one to two European settlement at 1788 marks a particularly profound extinctions per decade) is likely to continue. Australia’s marine historical landmark for the Australian environment, the opening mammals have fared better overall, but status assessment for up of the continent to a diverse array of new factors, and an ap- them is seriously impeded by lack of information.
    [Show full text]
  • Phylogenetic Relationships and Divergence Times in Rodents Based on Both Genes and Fossils Ryan Norris University of Vermont
    University of Vermont ScholarWorks @ UVM Graduate College Dissertations and Theses Dissertations and Theses 2009 Phylogenetic Relationships and Divergence Times in Rodents Based on Both Genes and Fossils Ryan Norris University of Vermont Follow this and additional works at: https://scholarworks.uvm.edu/graddis Recommended Citation Norris, Ryan, "Phylogenetic Relationships and Divergence Times in Rodents Based on Both Genes and Fossils" (2009). Graduate College Dissertations and Theses. 164. https://scholarworks.uvm.edu/graddis/164 This Dissertation is brought to you for free and open access by the Dissertations and Theses at ScholarWorks @ UVM. It has been accepted for inclusion in Graduate College Dissertations and Theses by an authorized administrator of ScholarWorks @ UVM. For more information, please contact [email protected]. PHYLOGENETIC RELATIONSHIPS AND DIVERGENCE TIMES IN RODENTS BASED ON BOTH GENES AND FOSSILS A Dissertation Presented by Ryan W. Norris to The Faculty of the Graduate College of The University of Vermont In Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy Specializing in Biology February, 2009 Accepted by the Faculty of the Graduate College, The University of Vermont, in partial fulfillment of the requirements for the degree of Doctor of Philosophy, specializing in Biology. Dissertation ~xaminationCommittee: w %amB( Advisor 6.William ~il~atrickph.~. Duane A. Schlitter, Ph.D. Chairperson Vice President for Research and Dean of Graduate Studies Date: October 24, 2008 Abstract Molecular and paleontological approaches have produced extremely different estimates for divergence times among orders of placental mammals and within rodents with molecular studies suggesting a much older date than fossils. We evaluated the conflict between the fossil record and molecular data and find a significant correlation between dates estimated by fossils and relative branch lengths, suggesting that molecular data agree with the fossil record regarding divergence times in rodents.
    [Show full text]