House Mouse Plagues in Australia

Total Page:16

File Type:pdf, Size:1020Kb

House Mouse Plagues in Australia House mouse plagues in Australia Chris Dickman Introduced Rodent Pests in Australia House Mouse Black Rat Brown Rat (Mus musculus) (Rattus rattus) (Rattus norvegicus) Mus musculus in Australia • Arrived with European settlement (225 years ago)? • Now continent-wide • A pest in wheat-growing areas in southern regions • Outcompeted by native mice elsewhere • Prey source for owls, introduced and native mammalian carnivores Australian environments - 1 • Summer rain Winter or year round rain 0 500 1000 1500 2000 2500 3000 3500 Kilometers Australian environments - 2 Australian fauna – 1 Australian fauna – 2 Australian fauna – predators House Mouse life-history • Exist in small demes for long periods • These demes are in refuge sites: water, food, shelter • Rapid population turnover • Populations irrupt within 3-4 months when conditions are good, collapse within a year • Characteristics of an invasive species House Mouse reproduction • Gestation = 19 days • Sexual maturity = 5 – 6 weeks • Postpartum oestrus, 3-4 weeks between litters • Litter size = 1 –13 • Can breed year-round but not much in winter • Survival rates are low (<5%) during dry times, >40% after rain Mouse plagues in Australia Mouse plagues in Australia • >750 mice per hectare (but typically >1000 mice per hectare) • Since 1890 mouse plagues have been recorded ∼ every 10 years, but the frequency is increasing to every 4 years Where do mouse plagues occur? Darlings Downs Murrumbidgee Irrigation Area Victorian mallee How much is known about plague formation? • 70% of mouse plagues can be predicted by current models • Rainfall (early- and late-season rains), moderate temperatures, food availability, refuges are all important components of the current predictive models • Models are simple: plagues occur in regions where all native rodents & most marsupials are extinct, and mammalian predators are controlled Predicting house mouse plagues Rainfall grasses, crops, Food supplies seeds, insects ? Mouse births, deaths, demography movements 70% predictability Complicating factors Crop damage predation, disease social interactions Krebs et al. (2005) Impacts of House Mice • Economic costs • Social costs • Health costs • Environmental costs Economic costs • Significant crop loss and damage to stored grain, damage to rural town businesses (e.g., stock spoilage, destruction of electrical cabling) • Outbreak in 1993 cost up to $Aus 100 million in losses, most costs borne by grain growers • In South Australia, 350 000 ha baited with strychnine • More-recent outbreaks have cost > $Aus 100 M Farming practices and mouse plagues • Clearing remnant areas of native vegetation disadvantages predators • Mammalian predators are culled • Retaining ground cover to prevent soil loss and retain soil moisture lowers predation risk for mice • Crop rotation and continuous cropping • Irrigation provides permanently good conditions • (Pech et al. 1999; Kenney et al. 2003) Rodenticides used in Australia • Alphachlorlose (not used much) • Bodifacoum • Bromadiolone • Cholecalciferol (withdrawn) • Coumatetrayl • Flocoumafen • Sodium monofluoacetate (1080) • Strychnine • Thallium sulphate (withdrawn) • Warfarin (Ratsak) • Zinc phosphide Immunocontraception Dynamics of native mice Lessons for mouse plagues? • NE Simpson Desert, Queensland • Spinifex-dominated dunefields • Rainfall 150-200 mm year-1 • Temperatures -7 to 50°C • Fire return interval ~25 years • Long-term data 1990-present • > 25,000 mammal captures, ~22,000 lizard captures, ~9,500 frogs Boom and bust dynamics – native mice Average of Pseudomys hermannsburgensis 60 50 Sandy inland mouse Sandy inland mouse Pseudomys 40 hermannsburgensis 30 20 Captures trap (100 nights) Photo by Bobby Tamayo 10 0 1990 1991 1993 Average of1999 Notomys2001 alexis2002 2006 2008 2011 60 50 Spinifex hopping-mouse 40 30 Captures trap (100 nights) 20 10 0 1990 1991 1993 1999 2001 2002 2006 2008 2011 Captures (100 trap nights) Rainfall (mm) 10 20 30 40 50 60 300 350 400 100 150 200 250 0 50 0 1990 1990 of rain mice: effects Native 1990 1991 1990 1991 Sandy inland mouse, 1991 1992 1993 1992 Long 1992 1993 1993 1994 - 6 1994 rainfall termannual‘average’ - Average of Pseudomys Average hermannsburgensis month lag 1995 1995 1995 1996 1996 1997 1997 1997 r 1998 = 0.66*** 1998 1999 1999 1999 2000 2000 2000 2001 2001 2001 2002 2002 2002 2002 2003 2003 2004 Sandy inland inland Sandy 2004 hermannsburgensis 2005 2005 mouse Photo by Bobby Tamayo Bobby by Photo 2005 Pseudomys 2006 2006 2006 2007 2007 2007 – 2008 2008 2008 2009 1 2009 2010 2010 2010 2011 2011 2011 Captures (100 trap nights) Rainfall (mm) 60 10 20 30 40 50 300 350 400 100 150 200 250 0 50 0 1990 1990 of rain mice: effects Native 1990 1991 1990 1991 1991 Spinifexhoppingmouse, 1992 Long 1993 1992 1992 1993 - 1993 rainfall termannual‘average’ 1994 6 1994 - 1995 month lag 1995 1995 1996 1996 Average of alexis Notomys Average 1997 1997 1997 1998 1998 1999 1999 r 1999 =0.47*** 2000 2000 2000 2001 2001 2001 2002 2002 2002 2002 2003 2003 2004 2004 2005 2005 2005 2006 2006 2006 2007 2007 2007 – 2008 2008 2008 2009 2 2009 2010 2010 2010 2011 2011 2011 Captures (100 trap nights) Rainfall (mm) 0.5 1.5 2.5 3.5 4.5 100 150 200 250 300 350 400 50 0 1 2 3 4 5 0 1990 1990 Marsupials: effects of rain of rain effects Marsupials: 1990 1991 1990 1991 1991 Long 1992 Brush 1992 1993 1992 Long 1993 - 1993 rainfall termannual‘average’ 1994 - - tailedmulgara, 1994 term annual ‘average’ rainfall termannual‘average’ 1995 10 1995 Average of1995 Dasycercus cristicauda - month lag 1996 1996 1997 1997 1997 1998 1998 r 1999 1999 = 0.58*** 1999 2000 2000 2000 2001 2001 2001 2002 2002 2002 2002 2003 2003 2004 2004 2005 2005 2005 2006 2006 2006 2007 2007 2007 – 2008 2008 2008 1 2009 2009 2010 2010 2010 2011 2011 2011 Rainfall (mm) Captures (100 trap nights) 100 150 200 250 300 350 400 50 0 1 2 3 4 5 6 7 8 0 1990 1990 1990 Marsupials: effects of rain of rain effects Marsupials: 1991 1990 1991 1991 dunnart, Lesser hairy 2 1992 - 1992 6 month lag 1993 1992 1993 1993 Long 1994 r 1994 = 1995 1995 - - - term annual ‘average’ rainfall termannual‘average’ 0.33** footed 1995 Average of SminthopsisAverage youngsoni 1996 1996 1997 1997 1997 1998 1998 1999 1999 1999 2000 2000 2000 2001 2001 2001 2002 2002 2002 2002 2003 2003 2004 2004 2005 2005 2005 2006 2006 2006 2007 2007 2007 – 2008 2008 2008 2009 2 2009 2010 2010 2010 2011 2011 2011 Effects of predators Average of Pseudomys hermannsburgensis 60 Capture rate: Sandy inland mouse 50 Heavy summer rains 40 Rains 30 20 Intense per capita predation Predation Captures trap (100 nights) 10 0 1990 1991 1993 1999 2001 2002 2006 2008 2011 Conclusions • Invasive rodents such as house mice show many of the characteristics of invasive species • Plagues are predictable: shelter, rainfall → food allows increased breeding & survival • Ecological, economic, health and broader environmental coats are immense • Traditional control techniques have variable (and often questionable) effects • Need for new control measures – lessons from native rodent dynamics References • Brown P.R. & Singleton G.R. 1999 J Applied Ecology 36: 484-493 • Dickman C.R. et al. 2011 J Mammalogy 92: 1193-1209 • Kenney A.J. et al. 2003 Pages 325-328 in Rats, Mice and People, ed. G.R. Singleton et al. ACIAR Monograph series, Canberra • Krebs C.J. et al. 2005 Wildlife Research 31: 465-474 • Pech, R.P. et al. 1999 Pages 81-112 in Ecologically-based Management of Rodent Pests, ed. G.R. Singleton et al. ACIAR Monograph series, Canberra • Singleton G.R. 1989 Journal of Zoology 219: 495-515 • White T.C.R. 2002 Australian J. Agricultural Research 53: 505- 509 • Ylönen H. et al. 2003 Oecologia 135: 372-377 .
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]
  • 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]
  • Mammals of the Avon Region
    Mammals of the Avon Region By Mandy Bamford, Rowan Inglis and Katie Watson Foreword by Dr. Tony Friend R N V E M E O N G T E O H F T W A E I S L T A E R R N A U S T 1 2 Contents Foreword 6 Introduction 8 Fauna conservation rankings 25 Species name Common name Family Status Page Tachyglossus aculeatus Short-beaked echidna Tachyglossidae not listed 28 Dasyurus geoffroii Chuditch Dasyuridae vulnerable 30 Phascogale calura Red-tailed phascogale Dasyuridae endangered 32 phascogale tapoatafa Brush-tailed phascogale Dasyuridae vulnerable 34 Ningaui yvonnae Southern ningaui Dasyuridae not listed 36 Antechinomys laniger Kultarr Dasyuridae not listed 38 Sminthopsis crassicaudata Fat-tailed dunnart Dasyuridae not listed 40 Sminthopsis dolichura Little long-tailed dunnart Dasyuridae not listed 42 Sminthopsis gilberti Gilbert’s dunnart Dasyuridae not listed 44 Sminthopsis granulipes White-tailed dunnart Dasyuridae not listed 46 Myrmecobius fasciatus Numbat Myrmecobiidae vulnerable 48 Chaeropus ecaudatus Pig-footed bandicoot Peramelinae presumed extinct 50 Isoodon obesulus Quenda Peramelinae priority 5 52 Species name Common name Family Status Page Perameles bougainville Western-barred bandicoot Peramelinae endangered 54 Macrotis lagotis Bilby Peramelinae vulnerable 56 Cercartetus concinnus Western pygmy possum Burramyidae not listed 58 Tarsipes rostratus Honey possum Tarsipedoidea not listed 60 Trichosurus vulpecula Common brushtail possum Phalangeridae not listed 62 Bettongia lesueur Burrowing bettong Potoroidae vulnerable 64 Potorous platyops Broad-faced
    [Show full text]
  • Why Are Small Mammals Not Such Good Thermoregulators in Arid
    Are day-active small mammals rare and small birds abundant in Australian desert environments because small mammals are inferior thermoregulators? P. C. Withers1, C. E. Cooper1,2, and W.A. Buttemer3 1Zoology, School of Animal Biology M092, University of Western Australia, Crawley, WA 6009 2Present Address: Centre for Behavioural and Physiological Ecology, University of New England, Armidale, NSW 2351 3 Biological Sciences, Faculty of Science, University of Wollongong, Wollongong, NSW 2522 1 Abstract Small desert birds are typically diurnal and highly mobile (hence conspicuous) whereas small non-volant mammals are generally nocturnal and less mobile (hence inconspicuous). Birds are more mobile than terrestrial mammals on a local and geographic scale, and most desert birds are not endemic but simply move to avoid the extremes of desert conditions. Many small desert mammals are relatively sedentary and regularly use physiological adjustments to cope with their desert environment (e.g. aestivation or hibernation). It seems likely that prey activity patterns and reduced conspicuousness to predators have reinforced nocturnality in small desert mammals. Differences such as nocturnality and mobility simply reflect differing life-history traits of birds and mammals rather than being a direct result of their differences in physiological capacity for tolerating daytime desert conditions. Australian desert mammals and birds Small birds are much more conspicuous in Australian desert environments than small mammals, partly because most birds are diurnal, whereas most mammals are nocturnal. Despite birds having over twice the number of species as mammals (ca. 9600 vs. 4500 species, respectively), the number of bird species confined to desert regions is relatively small, and their speciation and endemism are generally low (Wiens 1991).
    [Show full text]
  • Eastern Range Extension of Pseudomys Hermannsburgensis in Queensland
    Eastern range extension of Pseudomys hermannsburgensis in Queensland A.S. Kutt1, C. Eddie2 and R. Johnson2 1 School of Tropical Biology and Australian Centre for Tropical Freshwater Research, James Cook University, Townsville, QLD 4811. Current address: Queensland Parks and Wildlife Service (Environmental Protection Agency), PO Box 5391, Townsville, QLD 4810. Email: [email protected]. gov.au 2 Queensland Parks and Wildlife Service, PO Box 981, Roma, QLD 4455. Downloaded from http://meridian.allenpress.com/australian-zoologist/article-pdf/32/2/252/1475744/az_2003_007.pdf by guest on 27 September 2021 Introduction The Sandy Inland Mouse Pseudomys hermannsburgensis Despite earlier contentions of the exclusive distribution and the Delicate Mouse P. delicatulus are two closely allied patterns of these two species, evidence exists for sympatry members of the largest genus of Australian rodents (Watts between P. hermannsburgensis and P. delicatulus in Western and Aslin 1981). Currently 22 species are recognised in Australia (How et al. 1991) and the Northern Territory the genus Pseudomys (Cole and Woinarski in press), (J. Cole pers. comm. 2002, Northern Territory though the taxonomy of this large group has variably been Department of Infrastructure, Planning and considered “a repository for species hard to classify” Environment). In Western Australia, both were trapped (Watts and Aslin 1981). Taxonomic reassessment of the together in three sites at the Abydos-Woodstock Reserve, group is ongoing (Breed and Aplin 1995; Breed 1996; F. in very low open Eucalyptus and Acacia woodland, with Ford, pers. comm. 2002, James Cook University). Triodia spp. ground cover and sandy soils (How et al. Pseudomys hermannsburgensis and P.
    [Show full text]
  • On Mammalian Sperm Dimensions J
    On mammalian sperm dimensions J. M. Cummins and P. F. Woodall Reproductive Biology Group, Department of Veterinary Anatomy, University of Queensland, St Lucia, Queensland4067, Australia Summary. Data on linear sperm dimensions in mammals are presented. There is infor- mation on a total of 284 species, representing 6\m=.\2%of all species; 17\m=.\2%of all genera and 49\m=.\2%of all families have some representation, with quantitative information missing only from the orders Dermoptera, Pholidota, Sirenia and Tubulidentata. In general, sperm size is inverse to body mass (except for the Chiroptera), so that the smallest known spermatozoa are amongst those of artiodactyls and the largest are amongst those of marsupials. Most variations are due to differences in the lengths of midpiece and principal piece, with head lengths relatively uniform throughout the mammals. Introduction There is increasing interest in comparative studies of gametes both from the phylogenetic viewpoint (Afzelius, 1983) and also in the analysis of the evolution of sexual reproduction and anisogamy (Bell, 1982; Parker, 1982). This work emerged as part of a review of the relationship between sperm size and body mass in mammals (Cummins, 1983), in which lack of space precluded the inclusion of raw data. In publishing this catalogue of sperm dimensions we wish to rectify this defect, and to provide a reference point for, and stimulus to, further quantitative work while obviating the need for laborious compilation of raw data. Some aspects of the material presented previously (Cummins, 1983) have been re-analysed in the light of new data. Materials and Methods This catalogue of sperm dimensions has been built up from cited measurements, from personal observations and from communication with other scientists.
    [Show full text]
  • NATIVE MICE and RATS BILL BREED and FRED FORD NATIVE MICE and RATS Photos Courtesy Jiri Lochman,Transparencies Lochman
    AUSTRALIAN NATURAL HISTORY SERIES AUSTRALIAN NATURAL HISTORY SERIES NATIVE MICE AND RATS BILL BREED AND FRED FORD BILL BREED AND RATS MICE NATIVE NATIVE MICE AND RATS Photos courtesy Jiri Lochman,Transparencies Lochman Australia’s native rodents are the most ecologically diverse family of Australian mammals. There are about 60 living species – all within the subfamily Murinae – representing around 25 per cent of all species of Australian mammals.They range in size from the very small delicate mouse to the highly specialised, arid-adapted hopping mouse, the large tree rat and the carnivorous water rat. Native Mice and Rats describes the evolution and ecology of this much-neglected group of animals. It details the diversity of their reproductive biology, their dietary adaptations and social behaviour. The book also includes information on rodent parasites and diseases, and concludes by outlining the changes in distribution of the various species since the arrival of Europeans as well as current conservation programs. Bill Breed is an Associate Professor at The University of Adelaide. He has focused his research on the reproductive biology of Australian native mammals, in particular native rodents and dasyurid marsupials. Recently he has extended his studies to include rodents of Asia and Africa. Fred Ford has trapped and studied native rats and mice across much of northern Australia and south-eastern New South Wales. He currently works for the CSIRO Australian National Wildlife Collection. BILL BREED AND FRED FORD NATIVE MICE AND RATS Native Mice 4thpp.indd i 15/11/07 2:22:35 PM Native Mice 4thpp.indd ii 15/11/07 2:22:36 PM AUSTRALIAN NATURAL HISTORY SERIES NATIVE MICE AND RATS BILL BREED AND FRED FORD Native Mice 4thpp.indd iii 15/11/07 2:22:37 PM © Bill Breed and Fred Ford 2007 All rights reserved.
    [Show full text]
  • UC Berkeley Electronic Theses and Dissertations
    UC Berkeley UC Berkeley Electronic Theses and Dissertations Title Elucidating the Evolutionary Consequences of Sociality Through Genome-wide Analyses of Social and Solitary Mammals Permalink https://escholarship.org/uc/item/8zr0f93f Author Crawford, Jeremy Chase Publication Date 2016 Peer reviewed|Thesis/dissertation eScholarship.org Powered by the California Digital Library University of California Elucidating the Evolutionary Consequences of Sociality Through Genome-wide Analyses of Social and Solitary Mammals By Jeremy Chase Crawford A dissertation submitted in partial satisfaction of the requirements for the degree of Doctor of Philosophy in Integrative Biology in the Graduate Division of the University of California, Berkeley Committee in charge: Professor Eileen A. Lacey, Chair Professor George E. Bentley Professor Montgomery W. Slatkin Professor Damian O. Elias Spring 2016 Elucidating the Evolutionary Consequences of Sociality Through Genome-wide Analyses of Social and Solitary Mammals Copyright © 2016 By Jeremy Chase Crawford Abstract Elucidating the Evolutionary Consequences of Sociality Through Genome-wide Analyses of Social and Solitary Mammals by Jeremy Chase Crawford Doctor of Philosophy in Integrative Biology University of California, Berkeley Professor Eileen A. Lacey, Chair Social affiliation and group living are seminal aspects of some of the most exciting and intensely studied topics in behavioral biology, from the field of human psychopathology to investigations of cooperation and reproductive skew in animal societies. Understanding how and why sociality evolves as an alternative to the much more common trait of solitary living has long been a topic of special interest among biologists, particularly in light of evidence that group living can impose a number of costs (e.g., increased exposure to pathogens or increased resource competition) that can negatively impact direct fitness.
    [Show full text]
  • The Socio-Ecology of Two Species of Australian Native Rodent—Notomys
    The socio-ecology of two species of Australian native rodent— Notomys mitchelli and Notomys alexis Clare Bradley PhD candidate Environmental Biology School of Earth and Environmental Sciences University of Adelaide November 2008 References References Abramsky Z., Rosenweig M. L. & Subach A. (1998) Do gerbils care more about competition or predation? Oikos 83: 75-84. Abramsky Z., Rosenzweig M. L., Belmaker J. & Bar A. (2004) The impact of long-term continuous risk of predation on two species of gerbils. Canadian Journal of Zoology 82: 464-474. Abramsky Z., Rosenzweig M. L. & Subacha A. (2001) The cost of interspecific competition in two gerbil species. Journal of Animal Ecology 70: 561–567. Abramsky Z., Rosenzweig M. L. & Subacha A. (2002) Measuring the benefit of habitat selection. Behavioral Ecology 13: 497-502. Abramsky Z., Strauss E., Subach A., Kotler B. P. & Riechman A. (1996) The effect of barn owls (Tyto alba) on the activity and microhabitat selection of Gerbillus allenbyi and G. pyramidum. Oecologia 105: 313-319. Adams M., Macfarlane C. & Bencini R. (2003) Climate. In: Ecology: an Australian perspective (eds. P. Attiwill & B. Wilson) pp. 36-53. Oxford University Press, Victoria. Agrell J., Wolff J. O. & Ylonen H. (1998) Counter-strategies to infanticide in mammals: costs and consequences. Oikos 83: 507-517. Alexander R. D. (1974) The evolution of social behavior. Annual Review of Ecology and Systematics 5: 325-383. Allaine D. (2000) Sociality, mating system and reproductive skew in marmots: evidence and hypotheses. Behavioural Processes 51: 21-34. Allan R. (2003) El Niño. In: Ecology: an Australian perspective (eds. P. Attiwill & B.
    [Show full text]
  • Ecology and Conservation of the Northern Hopping-Mouse and Sympatric Vertebrates of Groote Eylandt
    Ecology and conservation of the northern hopping-mouse and sympatric vertebrates of Groote Eylandt Rebecca Diete Bachelor of Applied Science (Wildlife Science, Honours) A thesis submitted for the degree of Doctor of Philosophy at The University of Queensland in 2016 School of Agriculture and Food Science ii Abstract Effective monitoring is a critical component of wildlife management. The conservation of the enigmatic northern hopping-mouse (Notomys aquilo) has been impeded by poor understanding of the species’ ecology; an issue compounded by the lack of appropriate survey methods. Within a genus of largely arid-dwelling rodents, N. aquilo is the only extant species in Australia’s northern, monsoonal tropics where it is likely restricted to Groote Eylandt and a small area on the adjacent mainland. Surveys for N. aquilo have traditionally involved recording the location and abundance of indirect signs, as the species is trap-shy towards box-style traps, such as Elliott traps. One of the most important signs is the ‘spoil heap’ left by the construction of hopping-mouse burrows. Recent surveys for N. aquilo have relied almost entirely upon the identification of spoil heaps; however, the effectiveness of these methods has been questioned. This study aimed to fill key gaps in this knowledge by: (1) evaluating the effectiveness of spoil heap surveys for determining the presence and abundance of N. aquilo; (2) developing more-reliable survey methods for N. aquilo and sympatric vertebrates; and (3) describing the general ecology of N. aquilo with views to its conservation on Groote Eylandt. A novel use of video camera traps allowed the recording of burrow construction by N.
    [Show full text]
  • Overview of the Impact of Feral Cats on Australian Native Fauna
    OVERVIEW OF THE IMPACTS OF FERAL CATS ON AUSTRALIAN NATIVE FAUNA by Chris R. Dickman Institute of Wildlife Research and School of Biological Sciences University of Sydney Prepared for the Australian Nature Conservation Agency 1996 AUSTRALIA Overview of the Impacts of Feral Cats on Australian Native Fauna by Chris Dickman The views and opinions expressed in this report are those of the authors and do not necessarily reflect those of the Commonwealth Government, the Minister for the Environment or the Director of National Parks and Wildlife. ISBN 0 642 21379 8 Published May 1996 © Copyright The Director of National Parks and Wildlife Australian Nature Conservation Agency GPO Box 636 Canberra ACT 2601 and Institute of Wildlife Research University of Sydney Sydney NSW 2006 Design and art production by BPD Graphic Associates, Canberra Cover illustration by Karina Hansen McInnes CONTENTS FOREWORD 1 SUMMARY 2 EXECUTIVE SUMMARY AND RECOMMENDATIONS 3 ACKNOWLEDGEMENTS 4 1. INTRODUCTION 5 1.1 Scope of the report 5 2. DEFINITIONS 7 3. IMPACTS OF DOMESTIC AND STRAY CATS 9 3.1 Competitive impacts of domestic and stray cats 9 3.2 Predatory impacts of domestic and stray cats 9 3.3 Amensal impacts of domestic and stray cats 13 3.4 Summary: impacts of domestic and stray cats 14 4. IMPACTS OF FERAL CATS 15 4.1 Competitive impacts of feral cats 15 4.2 Predatory impacts of feral cats 16 4.2.1 Diets of feral cats: mainland only 16 4.2.2 Diets of feral cats: islands 18 4.2.3 Hunting behaviour of feral cats 18 4.2.4 Predatory impacts: what constitutes acceptable evidence? 19 - Predatory impacts: anecdotal evidence 19 Predatory impacts: historical evidence 20 - Predatory impacts: evidence from reintroduction programs 23 - Predatory impacts: evidence from islands 26 - Predatory impacts: field experiments 32 4.3 Amensal impacts of feral cats 33 4.3.1 Pathogens 33 4.3.2 Other indirect effects 36 4.4 Summary: impacts of feral cats 37 5.
    [Show full text]
  • Rattus Tunneyi) at Heirisson Prong, Shark Bay, Western Australia
    RESEARCH REPOSITORY This is the author’s final version of the work, as accepted for publication following peer review but without the publisher’s layout or pagination. The definitive version is available at: https://doi.org/10.1071/AM16028 Short, J., O'Neill, S. and Richards, Jacqueline D. (2017) Irruption and collapse of a population of pale field-rat (Rattus tunneyi) at Heirisson Prong, Shark Bay, Western Australia. Australian Mammalogy, In press. http://researchrepository.murdoch.edu.au/id/eprint/37200/ Copyright: © Australian Mammal Society 2017. It is posted here for your personal use. No further distribution is permitted. Pale field rat on HP_review.doc 18/06/2017 Irruption and collapse of a population of pale field-rat 2 Rattus tunneyi at Heirisson Prong, Shark Bay, Western Australia 4 6 Jeff ShortA, B, C, Sally O’NeillB and Jacqueline D. RichardsA ACSIRO Sustainable Ecosystems, Wembley, WA, 6913. 8 BFaculty of Sustainability, Environmental and Life Science, Murdoch University, South Street, Murdoch, WA, 6150. 10 CCurrent address: Wildlife Research and Management Pty Ltd, P.O. Box 1360, Kalamunda, WA, 6926. Email: [email protected] 12 Abstract. Pale field-rats have long disappeared from Australia’s arid and semi- 14 arid zones, other than for some Pilbara islands and a single mainland population of indeterminate status and extent identified at Shark Bay in 1968. Hence, it was 16 noteworthy when a field-rat was first caught at Heirisson Prong in 1994, 40 kilometres north-east of the previous location at Shark Bay. Further individuals were 18 caught regularly from late 1995. The population peaked in July to October 2000 (with captures of c.
    [Show full text]