Male-biased movement in pygmy bluetongue lizards: implications for conservation
Julie A. Schofield A B , Aaron L. Fenner A , Kelly Pelgrim A and C. Michael Bull AA School of Biological Sciences, Flinders University, GPO Box 2100, Adelaide, SA 5001, Australia.
B Corresponding author. Email: Julie.Schofield@flinders.edu.au
Wildlife Research 39(8) 677-684 https://doi.org/10.1071/WR12098
Submitted: 2 January 2012 Accepted: 10 September 2012 Published: 30 October 2012
Abstract
Context: Translocation has become an increasingly common tool in the conservation of species. Understanding the movement patterns of some species can be important to minimise loss of individuals from the translocation release site.
Aims: To describe seasonal and sex-biased movements within populations of an endangered Australian lizard.
Methods: We monitored seasonal movement in the endangered pygmy bluetongue lizard (Tiliqua adelaidensis) by using pitfall trapping, with a total of 49 440 trap-nights from three sites over 2 years. Other studies have shown that individual pygmy bluetongue lizards normally remained closely associated with their spider burrow refuges, with very little movement. Thus, we interpreted any captures detected through pitfall trapping as out of burrow movements. We investigated whether there was any seasonal, age or sex bias in moving individuals.
Key results: We found that male pygmy bluetongue lizards were more likely to move than were females. After adults, neonates were the second-most captured age class. Spring was the peak movement time for adults, whereas movement of neonates occurred in autumn.
Key conclusions: The majority of movement can be attributed to males in the breeding season, whereas females move very little.
Implications: The present study provides some baseline data that would allow more informed decisions about the most appropriate individuals in a population to choose for a translocation program and the times to conduct translocations to allow the maximum chance for establishment.
References
Andrewartha, H. G., and Birch, L. C. (1984). ‘The Ecological Web: More on the Distribution and Abundance of Animals.’ (The Univeristy of Chicago Press: Chicago, IL.)Armstrong, G., and Reid, J. (1992). The rediscovery of the Adelaide pygmy bluetongue lizard Tiliqua adelaidensis; (Peters, 1863). Herpetofauna 22, 3–6.
Armstrong, G., and Reid, J. (1993). Discovery of a population of the rare scincid lizard, Tiliqua adeliadensis (Peters). Records of the South Australian Mueseum 36, 53–55.
Bouzat, J. L., Johnson, J. A., Toepfer, J. E., Simpson, S. A., Esker, T. L., and Westemier, R. L. (2009). Beyond the beneficial effects of translocations as an effective tool for the genetic restoration of isolated populations. Conservation Genetics 10, 191–201.
| Beyond the beneficial effects of translocations as an effective tool for the genetic restoration of isolated populations.Crossref | GoogleScholarGoogle Scholar |
Bureau of Meteorology (2012). Australian Government Bureau of Meteorology. Available at http://www.bom.gov.au/ [verified 18 September 2012].
Calsbeek, R. (2009). Sex-specific adult dispersal and its selective conasquences in the brow anole, Anolis sagrei. Journal of Animal Ecology 78, 617–624.
Chapple, D. G., and Keogh, J. S. (2006). Group structure and stability in social aggreations of White’s skink, Egernia whitii. Ethology 112, 247–257.
| Group structure and stability in social aggreations of White’s skink, Egernia whitii.Crossref | GoogleScholarGoogle Scholar |
Clobert, J., Danchin, E., Dhondt, A. A., and Nichols, J. D. (Eds) (2001). ‘Dispersal.’ (Oxford University Press: New York.)
Clobert, J., De Fraipont, M., and Danchin, E. (2008). Evolution of dispersal. In ‘Behavioural Ecology’. (Eds E. Danchin, L. Giraldeau and F. Cezilly.) (Oxford Universty Press: Oxford, UK.)
Clobert, J., Le Galliard, J. F., Cote, J., Meylan, S., and Massot, M. (2009). Informed dispersal, heterogeneity in animal dispersal syndromes and the dynamics of spatially structured populations. Ecology Letters 12, 197–209.
| Informed dispersal, heterogeneity in animal dispersal syndromes and the dynamics of spatially structured populations.Crossref | GoogleScholarGoogle Scholar |
Croft, D. P., Albanese, B., Arrowsmith, B. J., Botham, M., Webster, M., and Krause, J. (2003). Sex-biased movement in the guppy (Poecilia reticulata). Oecologica. 137, 62–68.
| Sex-biased movement in the guppy (Poecilia reticulata).Crossref | GoogleScholarGoogle Scholar |
Cunningham, A. A. (1996). Disease risks of wildlife translocations. Conservation Biology 10, 349–353.
| Disease risks of wildlife translocations.Crossref | GoogleScholarGoogle Scholar |
Dobson, F. S., and Jones, W. T. (1985). Multiple causes of dispersal. American Naturalist 126, 855–858.
| Multiple causes of dispersal.Crossref | GoogleScholarGoogle Scholar |
Doughty, P., Sinervo, B., and Burghardt, G. M. (1994). Sex-biased dispersal in a polgynous lizard, Uta stansburiana. Animal Behaviour 47, 227–229.
| Sex-biased dispersal in a polgynous lizard, Uta stansburiana.Crossref | GoogleScholarGoogle Scholar |
Dubey, S., and Shine, R. (2010). Restricted dispersal and genetic diversity in populations of an endangered montane lizard (Eulamprus leuraensis, Scincidae). Molecular Ecology 19, 886–897.
| Restricted dispersal and genetic diversity in populations of an endangered montane lizard (Eulamprus leuraensis, Scincidae).Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC3czisVSruw%3D%3D&md5=e4129e5547abb8ea02d702bd08e8f852CAS |
Fellows, H. L. (2008). Temporal and spatial dynamics of the endangered pygmy bluetongue lizard, Tiliqua adelaidensis: implications for translocation attempts. B.Sc.(Hon) Thesis. The Flinders University of South Australia, Adelaide.
Fellows, H. L., Fenner, A., and Bull, C. M. (2009). Spiders provide an important resource for an endangerd lizard. Journal of Zoology 279, 156–163.
Fenner, A., and Bull, C. M. (2007). Short-term impact of grassland fire on the endangered pygmy bluetongue lizard. Journal of Zoology 272, 444–450.
| Short-term impact of grassland fire on the endangered pygmy bluetongue lizard.Crossref | GoogleScholarGoogle Scholar |
Fenner, A., Bull, C. M., and Hutchinson, M. N. (2008). Injuries to lizards: conservation implications for the endangered pygmy bluetongue lizard (Tiliqua adelaidensis). Wildlife Research 35, 158–161.
Fenner, A. L., and Bull, C. M. (2009). Tiliqua adelaidensis (pygmy bluetongue lizard) mating behaviour. Herpetological Review 40, 91–92.
Fenner, A. L., and Bull, C. M. (2011). Central-place territorial defence in a burrow-dwelling skink: aggressive responses to conspecific models in pygmy bluetongue lizards. Journal of Zoology 283, 45–51.
| Central-place territorial defence in a burrow-dwelling skink: aggressive responses to conspecific models in pygmy bluetongue lizards.Crossref | GoogleScholarGoogle Scholar |
Fenner, A., Bull, C. M., and Hutchinson, M. N. (2007). Omnivorous diet of the endangered pygmy bluetongue lizard, Tiliqua adelaidensis. Amphibia-Reptilia 28, 560–565.
| Omnivorous diet of the endangered pygmy bluetongue lizard, Tiliqua adelaidensis.Crossref | GoogleScholarGoogle Scholar |
Gardner, M. G., Bull, C. M., Cooper, S. J. B., and Duffield, G. A. (2001). Genetic evidence for a family structure in stable social aggregations of the Australian lizard Egernia stokesii. Molecular Ecology 10, 175–183.
| Genetic evidence for a family structure in stable social aggregations of the Australian lizard Egernia stokesii.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD3MvitFOisw%3D%3D&md5=db10815992a1df9b80a461c421c02dacCAS |
Gardner, M. G., Hugall, A. F., Donnellan, S. C., Hutchinson, M. N., and Foster, R. (2008). Molecular systematics of social skinks: phylogeny and taxonomy of the Egernia group (Reptilia: Scincidae). Zoological Journal of the Linnean Society 154, 781–794.
| Molecular systematics of social skinks: phylogeny and taxonomy of the Egernia group (Reptilia: Scincidae).Crossref | GoogleScholarGoogle Scholar |
Germano, J. M., and Bishop, P. J. (2009). Suitability of amphibians and reptiles for translocation. Conservation Biology 23, 7–15.
| Suitability of amphibians and reptiles for translocation.Crossref | GoogleScholarGoogle Scholar |
Greenwood, P. J. (1980). Mating systems, philopatry and dispersal in birds and mammals. Animal Behaviour 28, 1140–1162.
| Mating systems, philopatry and dispersal in birds and mammals.Crossref | GoogleScholarGoogle Scholar |
Herzig, A. L. (1995). Effects of population density on long-distance dispersal in the goldenrod beetle Trirhabda virgata. Ecology 76, 2044–2054.
| Effects of population density on long-distance dispersal in the goldenrod beetle Trirhabda virgata.Crossref | GoogleScholarGoogle Scholar |
Hutchinson, MN, Milne, T, and Croft, T (1994). Redescription and ecological notes on the pygmy bluetongue, Tiliqa adelaidensis (Squamata: Scincida). Transactions of the Royal Society of South Australia 188, 217–226.
Hyde, M. (1995). ‘The Temperate Grasslands of South Australia: their Compostion and Conservation Status.’ (World Wide Fund for Nature: Sydney.)
Ims, R. A., and Andreassen, H. P. (2005). Density-dependent dispersal and spatial population dynmics. Proceedings. Biological Sciences 272, 913–918.
| Density-dependent dispersal and spatial population dynmics.Crossref | GoogleScholarGoogle Scholar |
Kerr, G. D., and Bull, C. M. (2006). Movement patterns in the monogamous sleepy lizard (Tiliqua rugosa): effects of gender, drought, time of year and time of day. Journal of Zoology 269, 137–147.
| Movement patterns in the monogamous sleepy lizard (Tiliqua rugosa): effects of gender, drought, time of year and time of day.Crossref | GoogleScholarGoogle Scholar |
King, M. B., and Duvall, D. (1990). Prarie rattlesnake seasonal migrations: episodes of movement, vernal foraging and sex differnces. Animal Behaviour 39, 924–935.
| Prarie rattlesnake seasonal migrations: episodes of movement, vernal foraging and sex differnces.Crossref | GoogleScholarGoogle Scholar |
Lane, A., and Shine, R. (2011). Intraspecific variation in the direction and degree of sex-biased dispersal among sea-snake populations. Molecular Ecology 20, 1870–1876.
| Intraspecific variation in the direction and degree of sex-biased dispersal among sea-snake populations.Crossref | GoogleScholarGoogle Scholar |
Matthysen, E. (2005). Density-dependant dispersal in birds and mammals. Ecography 28, 403–416.
| Density-dependant dispersal in birds and mammals.Crossref | GoogleScholarGoogle Scholar |
Milne, T. (1999). Conservation and ecology of the endangered pygmy bluetongue lizard Tiliqua adelaidensis. Ph.D. Thesis. The Flinders University of South Australia, Adelaide.
Milne, T., Bull, C. M., and Hutchinson, M. N. (2002). Characteristics of litters and juvenile dispersal in the endangered Australian skink Tiliqua adelaidensis. Journal of Herpetology 36, 110–112.
Milne, T., Bull, C. M., and Hutchinson, M. N. (2003). Use of burrows by the endangered pygmy blue-tongue lizard, Tiliqua adelaidensis (Scincidae). Wildlife Research 30, 523–528.
| Use of burrows by the endangered pygmy blue-tongue lizard, Tiliqua adelaidensis (Scincidae).Crossref | GoogleScholarGoogle Scholar |
Moritz, C. (1999). Conservation units and translocations: strategies for conserving evolutionary processes. Hereditas 130, 217–228.
| Conservation units and translocations: strategies for conserving evolutionary processes.Crossref | GoogleScholarGoogle Scholar |
Moseby, K. E., Read, J. L., Paton, D. C., Copley, P., Hill, B. M., and Crisp, H. A. (2011). Predation determines outcome of 10 reintroduction attempts in South Australia. Biological Conservation 144, 2863–2872.
| Predation determines outcome of 10 reintroduction attempts in South Australia.Crossref | GoogleScholarGoogle Scholar |
Olsson, M., and Shine, R. (2003). Female-biased natal and breeding dispersal in an alpine lizard, Niveoscincus microlepidotus. Biological Journal of the Linnean Society. Linnean Society of London 79, 277–283.
| Female-biased natal and breeding dispersal in an alpine lizard, Niveoscincus microlepidotus.Crossref | GoogleScholarGoogle Scholar |
Olsson, M., Gullberg, A., and Tegelström, H. (1996). Malformed offspring, sibling matings, and selection against inbreeding in the sand lizard (Lacerta agilis). Journal of Evolutionary Biology 9, 229–242.
| Malformed offspring, sibling matings, and selection against inbreeding in the sand lizard (Lacerta agilis).Crossref | GoogleScholarGoogle Scholar |
Paquette, S. R., Rioux, S., Louis, E. E., and Lapointe, F. (2010). Microsatellite analyses provide evidence of male baised dispersal in the radiated tortoise Astrochelys radiata (Chelodonia: Testudinidae). The Journal of Heredity 101, 403–412.
| Microsatellite analyses provide evidence of male baised dispersal in the radiated tortoise Astrochelys radiata (Chelodonia: Testudinidae).Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXnvVOls7g%3D&md5=bfb624e7347c044049618bfc070a9a1aCAS |
Shier, D. M., and Swaisgood, R. R. (2012). Fitness costs of neighborhood disruption in translocations of a solitary mammal. Conservation Biology 26, 116–123.
| Fitness costs of neighborhood disruption in translocations of a solitary mammal.Crossref | GoogleScholarGoogle Scholar |
Smith, A. L., Gardner, M. G., Fenner, A. L., and Bull, C. M. (2009). Restricted gene flow in the endangered pygmy bluetongue lizard (Tiliqua adelaidensis) in a fragmented agricultural landscape. Wildlife Research 36, 466–478.
| Restricted gene flow in the endangered pygmy bluetongue lizard (Tiliqua adelaidensis) in a fragmented agricultural landscape.Crossref | GoogleScholarGoogle Scholar |
Souter, N. J. (2004). Habitat requirements and conservation of the endangered pygmy bluetongue lizard, Tiliqua adelaidensis. Ph.D. Thesis. The Flinders University of South Australia, Adelaide.
Souter, N., Bull, C. M., and Hutchinson, M. N. (2004). Adding burrows to enhance a population of the endangered pygmy blue tongue lizard, Tiliqua adelaidensis. Biological Conservation 116, 403–408.
| Adding burrows to enhance a population of the endangered pygmy blue tongue lizard, Tiliqua adelaidensis.Crossref | GoogleScholarGoogle Scholar |
Spoecker, P. D. (1967). Movements and seasonal activity cycles of the lizard Uta stansburiana stejnegeri. American Midland Naturalist 77, 484–494.
| Movements and seasonal activity cycles of the lizard Uta stansburiana stejnegeri.Crossref | GoogleScholarGoogle Scholar |
Stow, A. J., Sunnucks, P., Briscoe, D. A., and Garnder, M. G. (2001). The impact of habitat fragmentation on dispersal of Cunningham’s skink (Egernia cunninghami): evidence from allelic and genotypic analysis of microsatelites. Molecular Ecology 10, 867–878.
| The impact of habitat fragmentation on dispersal of Cunningham’s skink (Egernia cunninghami): evidence from allelic and genotypic analysis of microsatelites.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXjvVensbw%3D&md5=9d259434c01397af5e16766eddc72a2eCAS |
Temeles, E. J. (1994). The role of neighbours in territorial systems: when are they ‘dear enemies’? Animal Behaviour 47, 339–350.
| The role of neighbours in territorial systems: when are they ‘dear enemies’?Crossref | GoogleScholarGoogle Scholar |
Towns, D. R., and Ferreira, S. M. (2001). Conservation of New Zealand lizards (Lacertilia: Scincidae) by translocation of small populations. Biological Conservation 98, 211–222.
| Conservation of New Zealand lizards (Lacertilia: Scincidae) by translocation of small populations.Crossref | GoogleScholarGoogle Scholar |
Tucker, A. D., McCallum, H. J., Limpus, C. J., and McDonald, K. R. (1998). Sex-biased dispersal in a long-lived polygynous reptile (Crocodylus johnstoni). Behavioral Ecology and Sociobiology 44, 85–90.
| Sex-biased dispersal in a long-lived polygynous reptile (Crocodylus johnstoni).Crossref | GoogleScholarGoogle Scholar |
Ujvari, B., Dowton, M., and Madsen, T. (2008). Population genetic structure, gene flow and sex-biased dispersal in frillneck lizards (Chlamydosaurus kingii). Molecular Ecology 17, 3557–3564.
| 1:CAS:528:DC%2BD1cXhtVKgurrK&md5=7405f84eae0499c4d7fb7e0df81ee236CAS |
Weaver, R. E. (2010). Activity patterns of the desert nightsnake (Hypsiglena chlorophaea). The Southwestern Naturalist 55, 172–178.
| Activity patterns of the desert nightsnake (Hypsiglena chlorophaea).Crossref | GoogleScholarGoogle Scholar |