Excluding access to invasion hubs can contain the spread of an invasive vertebrate

Many biological invasions do not occur as a gradual expansion along a continuous front, but result from the expansion of satellite populations that become established at ‘invasion hubs’. Although theoretical studies indicate that targeting control efforts at invasion hubs can effectively contain the spread of invasions, few studies have demonstrated this in practice. In arid landscapes worldwide, humans have increased the availability of surface water by creating artificial water points (AWPs) such as troughs and dams for livestock. By experimentally excluding invasive cane toads (Bufo marinus) from AWP, we show that AWP provide a resource subsidy for non-arid-adapted toads and serve as dry season refuges and thus invasion hubs for cane toads in arid Australia. Using data on the distribution of permanent water in arid Australia and the dispersal potential of toads, we predict that systematically excluding toads from AWP would reduce the area of arid Australia across which toads are predicted to disperse and colonize under average climatic conditions by 38 per cent from 2 242 000 to 1 385 000 km2. Our study shows how human modification of hydrological regimes can create a network of invasion hubs that facilitates a biological invasion, and confirms that targeted control at invasion hubs can reduce landscape connectivity to contain the spread of an invasive vertebrate.

[1]  Richard Shine,et al.  Toad on the road: use of roads as dispersal corridors by cane toads (Bufo marinus) at an invasion front in tropical Australia. , 2006 .

[2]  R. Shine,et al.  Conditioned taste aversion enhances the survival of an endangered predator imperilled by a toxic invader , 2010 .

[3]  Simon Chamaillé-Jammes,et al.  Managing heterogeneity in elephant distribution: interactions between elephant population density and surface‐water availability , 2007 .

[4]  P. Shafroth,et al.  Altered stream-flow regimes and invasive plant species : the Tamarix case , 2007 .

[5]  S. Davies,et al.  Deconstructing a controversial local range expansion: conservation biogeography of the painted reed frog (Hyperolius marmoratus) in South Africa , 2007 .

[6]  R. Alford,et al.  Desiccation and shelter-site use in a tropical amphibian: comparing toads with physical models , 1996 .

[7]  P. Withers EVAPORATIVE WATER LOSS AND THE ROLE OF COCOON FORMATION IN AUSTRALIAN FROGS , 1998 .

[8]  Craig James,et al.  Provision of watering points in the Australian arid zone: a review of effects on biota , 1999 .

[9]  R. Shine,et al.  Abiotic and biotic influences on the dispersal behavior of metamorph cane toads (Bufo marinus) in tropical Australia. , 2008, Journal of experimental zoology. Part A, Ecological genetics and physiology.

[10]  P. Withers Metabolic depression during aestivation in the Australian frogs, Neobatrachus and Cyclorana , 1993 .

[11]  R. Shine,et al.  A Toad More Traveled: The Heterogeneous Invasion Dynamics of Cane Toads in Australia , 2008, The American Naturalist.

[12]  R. Alford,et al.  Shelter Microhabitats Determine Body Temperature and Dehydration Rates of a Terrestrial Amphibian (Bufo marinus) , 2002 .

[13]  M. V. Vander Zanden,et al.  Do Reservoirs Facilitate Invasions into Landscapes? , 2005 .

[14]  A. Suarez,et al.  Patterns of spread in biological invasions dominated by long-distance jump dispersal: Insights from Argentine ants. , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[15]  P. Hulme Trade, transport and trouble: managing invasive species pathways in an era of globalization , 2009 .

[16]  G. Zug,et al.  The marine toad, Bufo marinus : a natural history resumé of native populations , 1979 .

[17]  T. Dawson,et al.  Water use and the thermoregulatory behaviour of kangaroos in arid regions: insights into the colonisation of arid rangelands in Australia by the Eastern Grey Kangaroo (Macropus giganteus) , 2005, Journal of Comparative Physiology B.

[18]  Alan Hastings,et al.  Finding optimal control strategies for invasive species: a density‐structured model for Spartina alterniflora , 2004 .

[19]  Fritzi S. Grevstad,et al.  Simulating control strategies for a spatially structured weed invasion: Spartina alterniflora (Loisel) in Pacific Coast estuaries , 2005, Biological Invasions.

[20]  R. Shine,et al.  The extra‐limital spread of an invasive species via ‘stowaway’ dispersal: toad to nowhere? , 2009 .

[21]  Richard N. Mack,et al.  Controlling the spread of plant invasions: The importance of nascent foci. , 1988 .

[22]  H. MacIsaac,et al.  Development of inland lakes as hubs in an invasion network , 2005 .

[23]  David S. G. Thomas,et al.  Spreading deserts or spatially confined environmental impacts? land degradation and cattle ranching in the kalahari desert of botswana , 1993 .

[24]  B. Thompson,et al.  Wildlife Association with Human-Altered Water Sources in Semiarid Vegetation Communities , 1994 .

[25]  R. Sokal,et al.  Biometry: The Principles and Practice of Statistics in Biological Research (2nd ed.). , 1982 .

[26]  C. C. Grant,et al.  Do artificial waterholes influence the way herbivores use the landscape? Herbivore distribution patterns around rivers and artificial surface water sources in a large African savanna park , 2007 .

[27]  J. Covacevich,et al.  THE DISTRIBUTION OF THE CANE TOAD, BUFO MARINUS, IN AUSTRALIA AND ITS EFFECTS ON INDIGENOUS VERTEBRATES. , 1975 .

[28]  P. Hulme Beyond control : wider implications for the management of biological invasions , 2006 .

[29]  M. Knutson,et al.  AGRICULTURAL PONDS SUPPORT AMPHIBIAN POPULATIONS , 2004 .

[30]  B. Phillips,et al.  Toxic tucker: the potential impact of Cane Toads on Australian reptiles , 2006 .

[31]  J. Stromberg,et al.  Effects of Groundwater Decline on Riparian Vegetation of Semiarid Regions: The San Pedro, Arizona , 1996 .

[32]  R. Shine,et al.  Invasive cane toads (Bufo marinus) cause mass mortality of freshwater crocodiles (Crocodylus johnstoni) in tropical Australia , 2008 .

[33]  Richard Shine,et al.  Rapid expansion of the cane toad (Bufo marinus) invasion front in tropical Australia , 2007 .

[34]  R. Fensham,et al.  Water-remoteness for grazing relief in Australian arid-lands , 2008 .

[35]  Gregory P. Brown,et al.  Using a native predator (the meat ant, Iridomyrmex reburrus) to reduce the abundance of an invasive species (the cane toad, Bufo marinus) in tropical Australia , 2010 .

[36]  J. Reid Experimental Design and Data Analysis for Biologists , 2003 .

[37]  S. Setterfield,et al.  Shrub invasion of a tropical wetland: implications for weed management , 1996 .

[38]  D. Merritt,et al.  Shifting dominance of riparian Populus and Tamarix along gradients of flow alteration in western North American rivers. , 2010, Ecological applications : a publication of the Ecological Society of America.

[39]  M. Kearney,et al.  Modelling species distributions without using species distributions: the cane toad in Australia under current and future climates , 2008 .

[40]  D. Rhind,et al.  Population‐level declines in Australian predators caused by an invasive species , 2009 .

[41]  S. Higgins,et al.  A review of models of alien plant spread. , 1996 .

[42]  Kimberly A. With The Landscape Ecology of Invasive Spread , 2002 .

[43]  Anthony Ricciardi,et al.  Overland dispersal of aquatic invasive species: a risk assessment of transient recreational boating. , 2001 .

[44]  F. James Rohlf,et al.  Biometry: The Principles and Practice of Statistics in Biological Research , 1969 .

[45]  E. García‐Berthou,et al.  Invasive species are a leading cause of animal extinctions. , 2005, Trends in ecology & evolution.

[46]  A. Hyatt,et al.  Biological control of the cane toad in Australia: a review , 2010 .

[47]  S. Harrison,et al.  Local extinction in a metapopulation context: an empirical evaluation , 1991 .

[48]  G. Meyers,et al.  The Years of El Niño, La Niña, and Interactions with the Tropical Indian Ocean , 2007 .

[49]  Daniel Simberloff,et al.  Patterns of Extinction in the Introduced Hawaiian Avifauna: A Reexamination of the Role of Competition , 1991, The American Naturalist.