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Journal of BirdLife Australia
RESEARCH ARTICLE

Genetic structure and sex-biased dispersal of a declining cooperative-breeder, the Grey-crowned Babbler, Pomatostomus temporalis, at the southern edge of its range

Kate P. Stevens A D , Katherine A. Harrisson B , Rohan H. Clarke B , Raylene Cooke A and Fiona E. Hogan C
+ Author Affiliations
- Author Affiliations

A School of Life and Environmental Sciences, Deakin University, 221 Burwood Highway, Melbourne, Vic. 3125, Australia.

B School of Biological Sciences, Monash University, Melbourne, Vic. 3800, Australia.

C School of Applied and Biomedical Sciences, Federation University, PO Box 3191, Gippsland Mail Centre, Churchill, Vic. 3148, Australia.

D Corresponding author. Email: kstevens@deakin.edu.au

Emu 116(4) 323-332 https://doi.org/10.1071/MU15096
Submitted: 8 January 2015  Accepted: 5 March 2016   Published: 28 July 2016

Abstract

Loss and fragmentation of habitat can disrupt genetic exchange between populations, which is reflected in changes to the genetic structure of populations. The Grey-crowned Babbler (Pomatostomus temporalis) is a cooperatively breeding woodland bird, once common and widespread in south-eastern Australia. The species has suffered population declines of >90% across its southern distribution as a result of loss and fragmentation of habitat. We investigated patterns of genetic diversity and population structure of Grey-crowned Babblers in fragmented habitats at the southernmost extent of its range. We sampled blood from 135 individual Babblers from 39 groups stratified into six subpopulations in three regions. Genotypic data were used to estimate genetic diversity, population substructure, local relatedness and dispersal patterns. Individuals showed high heterozygosity within regions, and varying numbers of private alleles among regions suggested differences in levels of connectivity between regions. Four genetic clusters revealed population substructure consistent with treeless landscapes acting as strong barriers to gene flow. In contrast to previous studies, we identified a male-biased dispersal pattern and significant isolation-by-distance patterns for females at fine spatial scales. We recommend that conservation plans for this species incorporate opportunities to increase and enhance corridor areas to facilitate genetic exchange among subpopulations.

Additional keywords: corridors, functional connectivity, genetic diversity, habitat fragmentation, isolation-by-distance, regions.


References

Alda, F., Gonzalez, M. A., Olea, P. P., Ena, V., Godinho, R., and Drovetski, S. V. (2013). Genetic diversity, structure and conservation of the endangered Cantabrian Capercaillie in a unique peripheral habitat. European Journal of Wildlife Research 59, 719–728.
Genetic diversity, structure and conservation of the endangered Cantabrian Capercaillie in a unique peripheral habitat.Crossref | GoogleScholarGoogle Scholar |

Amos, J. N., Harrisson, K. A., Radford, J. Q., White, M., Newell, G., Mac Nally, R., Sunnucks, P., and Pavlova, A. (2014). Species- and sex-specific connectivity effects of habitat fragmentation in a suite of woodland birds. Ecology 95, 1556–1568.
Species- and sex-specific connectivity effects of habitat fragmentation in a suite of woodland birds.Crossref | GoogleScholarGoogle Scholar |

Bennett, A. F., Radford, J. Q., and Haslem, A. (2006). Properties of land mosaics: implication for nature conservation in agricultural environments. Biological Conservation 133, 250–264.
Properties of land mosaics: implication for nature conservation in agricultural environments.Crossref | GoogleScholarGoogle Scholar |

Blackmore, C. (2006). Breeding biology and behaviour of the Grey-crowned Babbler. PhD thesis, Australian National University, Canberra, ACT.

Blackmore, C. J., and Heinsohn, R. (2007). Reproductive success and helper effects in the cooperatively breeding Grey-crowned Babbler. Journal of Zoology 273, 326–332.
Reproductive success and helper effects in the cooperatively breeding Grey-crowned Babbler.Crossref | GoogleScholarGoogle Scholar |

Blackmore, C., and Heinsohn, R. (2008). Variable mating strategies and incest avoidance in cooperatively breeding Grey-crowned Babblers. Animal Behaviour 75, 63–70.
Variable mating strategies and incest avoidance in cooperatively breeding Grey-crowned Babblers.Crossref | GoogleScholarGoogle Scholar |

Blackmore, C. J., Adcock, G. J., Ebert, D., and Heinsohn, R. (2006). Microsatellite loci for population and behavioural studies of Grey-crowned Babblers (Pomatostomus temporalis:Aves). Molecular Ecology Notes 6, 412–414.
Microsatellite loci for population and behavioural studies of Grey-crowned Babblers (Pomatostomus temporalis:Aves).Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XmtlGqsbg%3D&md5=9692f0df563011bd05e6ded736070bc9CAS |

Blackmore, C. J., Peakall, R., and Heinsohn, R. (2011). The absence of sex-biased dispersal in the cooperatively breeding Grey-crowned Babbler. Journal of Animal Ecology 80, 69–78.
The absence of sex-biased dispersal in the cooperatively breeding Grey-crowned Babbler.Crossref | GoogleScholarGoogle Scholar | 21054379PubMed |

Bradshaw, C. J. A. (2012). Little left to lose: deforestation and forest degradation in Australia since European colonization. Journal of Plant Ecology 5, 109–120.
Little left to lose: deforestation and forest degradation in Australia since European colonization.Crossref | GoogleScholarGoogle Scholar |

Brown, J. L., Dow, D. D., Brown, E. R., and Brown, S. D. (1978). Effects of helpers on feeding of nestlings in the Grey-crowned Babbler (Pomatostomus temporalis). Behavioral Ecology and Sociobiology 4, 43–59.
Effects of helpers on feeding of nestlings in the Grey-crowned Babbler (Pomatostomus temporalis).Crossref | GoogleScholarGoogle Scholar |

Brown, J. L., Dow, D. D., Brown, E. R., and Brown, S. D. (1983). Socio-ecology of the Grey-crowned Babbler: population structure, unit size and vegetation correlates. Behavioral Ecology and Sociobiology 13, 115–124.
Socio-ecology of the Grey-crowned Babbler: population structure, unit size and vegetation correlates.Crossref | GoogleScholarGoogle Scholar |

Chen, C., Durand, E., Forbes, F., and Francois, O. (2007). Bayesian clustering algorithms ascertaining spatial population structure: a new computer program and a comparison study. Molecular Ecology Notes 7, 747–756.
Bayesian clustering algorithms ascertaining spatial population structure: a new computer program and a comparison study.Crossref | GoogleScholarGoogle Scholar |

Counsilman, J. J. (1979). Notes on the breeding biology of the Grey-crowned Babbler. Bird Behaviour 1, 114–124.
Notes on the breeding biology of the Grey-crowned Babbler.Crossref | GoogleScholarGoogle Scholar |

Counsilman, J. J., and King, B. (1977). Ageing and sexing the Grey-crowned Babbler (Pomatostomus temporalis). Bird Behaviour 1, 23–41.
Ageing and sexing the Grey-crowned Babbler (Pomatostomus temporalis).Crossref | GoogleScholarGoogle Scholar |

Crozier, L., and Dwyer, G. (2006). Combining population-dynamic and ecophysiological models to predict climate-induced insect range shifts. American Naturalist 167, 853–866.
Combining population-dynamic and ecophysiological models to predict climate-induced insect range shifts.Crossref | GoogleScholarGoogle Scholar | 16685639PubMed |

Cushman, S. A., McKelvey, K. S., and Schwartz, M. K. (2009). Use of empirically derived source-destination models to map regional conservation corridors. Conservation Biology 23, 368–376.
Use of empirically derived source-destination models to map regional conservation corridors.Crossref | GoogleScholarGoogle Scholar | 19016821PubMed |

Dale, S. (2001). Female-biased dispersal, low female recruitment, unpaired males, and the extinction of small and isolated bird populations. Oikos 92, 344–356.
Female-biased dispersal, low female recruitment, unpaired males, and the extinction of small and isolated bird populations.Crossref | GoogleScholarGoogle Scholar |

Davidson, I., and Robinson, D. (2009). Conservation plan for the Grey-crowned Babbler population in the Boort–Loddon district. Report for the North Central Catchment Management Authority and Department of Sustainability and Environment, Bendigo, Vic.

NSW Scientific Committee (2001). Grey-crowned Babbler (eastern subspecies) – vulnerable species listing. Final determination. NSW Office of Environment and Heritage, Sydney. Available at http://www.environment.nsw.gov.au/threatenedSpeciesApp/profile.aspx?id=10660 [Verified 15 August 2010].

Department of the Environment (2010). Australian Bird and Bat Banding Scheme Database Search: Pomatostomus temporalis (Grey-crowned Babbler). Australian Government, Canberra. Available at https://www.environment.gov.au/cgi-bin/biodiversity/abbbs/abbbs-search.pl [Verified 15 August 2010].

Develey, P. F., and Stouffer, P. C. (2001). Effects of roads on movements by understory birds in mixed-species flocks in central Amazonian Brazil. Conservation Biology 15, 1416–1422.
Effects of roads on movements by understory birds in mixed-species flocks in central Amazonian Brazil.Crossref | GoogleScholarGoogle Scholar |

Donald, P., Green, R., and Heath, M. (2001). Agricultural intensification and the collapse of Europe’s farmland bird populations. Proceedings of the Royal Society B: Biological Sciences 268, 25–29.
Agricultural intensification and the collapse of Europe’s farmland bird populations.Crossref | GoogleScholarGoogle Scholar |

Duncan, S. I., Crespi, E. J., Mattheus, N. M., and Rissler, L. J. (2015). History matters more when explaining genetic diversity within the context of the core-periphery hypothesis. Molecular Ecology 24, 4323–4336.
History matters more when explaining genetic diversity within the context of the core-periphery hypothesis.Crossref | GoogleScholarGoogle Scholar | 26175277PubMed |

Durand, E., Jay, F., Gaggiotti, O. E., and Francois, O. (2009). Spatial inference of admixture proportions and secondary contact zones. Molecular Biology and Evolution 26, 1963–1973.
Spatial inference of admixture proportions and secondary contact zones.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXhtVWhs7vJ&md5=a21baac970130f40019b8a00da4333ceCAS | 19461114PubMed |

Dutta, T., Sharma, S., Maldonado, J. E., Wood, T. C., Panwar, H. S., and Seidensticker, J. (2013). Fine-scale population genetic structure in a wide-ranging carnivore, the Leopard (Panthera pardus fusca) in central India. Diversity & Distributions 19, 760–771.
Fine-scale population genetic structure in a wide-ranging carnivore, the Leopard (Panthera pardus fusca) in central India.Crossref | GoogleScholarGoogle Scholar |

Edwards, S. V. (1993a). Mitochondrial gene genealogy and gene flow among island and mainland populations of a sedentary songbird, the Grey-crowned Babbler (Pomatostomus temporalis). Evolution 47, 1118–1137.
Mitochondrial gene genealogy and gene flow among island and mainland populations of a sedentary songbird, the Grey-crowned Babbler (Pomatostomus temporalis).Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2MXht1Wjsg%3D%3D&md5=559682cc7fa73d93400cd86ce0675f1bCAS |

Edwards, S. V. (1993b). Long-distance gene flow in a cooperative breeder detected in genealogies of mitochondrial-DNA sequences. Proceedings of the Royal Society B: Biological Sciences 252, 177–185.
Long-distance gene flow in a cooperative breeder detected in genealogies of mitochondrial-DNA sequences.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2cXhsF2gsbw%3D&md5=939b7ca9c7da479d1a5351954200f74eCAS | 8394578PubMed |

Eguchi, K., Yamaguchi, N., Ueda, K., Nagata, H., Takagi, M., and Noske, R. (2007). Social structure and helping behaviour of the Grey-crowned Babbler, Pomatostomus temporalis. Journal für Ornithologie 148, 203–210.
Social structure and helping behaviour of the Grey-crowned Babbler, Pomatostomus temporalis.Crossref | GoogleScholarGoogle Scholar |

Environment Conservation Council (2001). Box–ironbark forests and woodlands investigation. Final report. Environmental Conservation Council, Victoria. Available at http://www.veac.vic.gov.au/reports/385-BI-Complete-Report.pdf [Verified 3 March 2010].

Epps, C. W., Palsbøll, P. J., Wehausen, J. D., Roderick, G. K., Ramey, R. R., and McCullough, D. R. (2005). Highways block gene flow and cause a rapid decline in genetic diversity of Desert Bighorn Sheep. Ecology Letters 8, 1029–1038.
Highways block gene flow and cause a rapid decline in genetic diversity of Desert Bighorn Sheep.Crossref | GoogleScholarGoogle Scholar |

Epps, C. W., Wehausen, J. D., Bleich, V. C., Torres, S. G., and Brashares, J. S. (2007). Optimizing dispersal and corridor models using landscape genetics. Journal of Applied Ecology 44, 714–724.
Optimizing dispersal and corridor models using landscape genetics.Crossref | GoogleScholarGoogle Scholar |

Esri (2010). ‘ArcMap.’ Version 10.1. (Esri, Redlands, CA.)

Ford, H. A., Barret, G. W., Saunders, D. A., and Recher, H. F. (2001). Why have birds in the woodlands of southern Australia declined? Biological Conservation 97, 71–88.
Why have birds in the woodlands of southern Australia declined?Crossref | GoogleScholarGoogle Scholar |

Frankham, R. (1996). Relationship of genetic variation to population size in wildlife. Conservation Biology 10, 1500–1508.
Relationship of genetic variation to population size in wildlife.Crossref | GoogleScholarGoogle Scholar |

Frankham, R. (2005). Genetics and extinction. Biological Conservation 126, 131–140.
Genetics and extinction.Crossref | GoogleScholarGoogle Scholar |

Garnett, S. T., Szabo, J. K., and Dutson, G. (2011). ‘The Action Plan for Australian Birds 2010.’ (CSIRO Publishing: Melbourne, Vic.)

Gill, B. J., and Dow, D. D. (1985). Waking and roosting of Grey-crowned Babblers Pomatostomus temporalis, in south-east Queensland during spring. Emu 85, 97–105.
Waking and roosting of Grey-crowned Babblers Pomatostomus temporalis, in south-east Queensland during spring.Crossref | GoogleScholarGoogle Scholar |

Goudet, J. (1995). FSTAT version 1.2: a computer program to calculate f-statistics. Journal of Heredity 86, 485–486.

Griffiths, R., Double, M. C., Orr, K., and Dawson, R. J. G. (1998). A simple DNA test to sex most birds. Molecular Ecology 7, 1071–1075.
A simple DNA test to sex most birds.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXlslGmt7c%3D&md5=f39204166fad6fbe9b7270415a8182d3CAS | 9711866PubMed |

Guo, Q., Taper, M., Schoenberger, M., and Brandle, J. (2005). Spatial-temporal population dynamics across species range: from centre to margin. Oikos 108, 47–57.
Spatial-temporal population dynamics across species range: from centre to margin.Crossref | GoogleScholarGoogle Scholar |

Harrisson, K. A., Pavlova, A., Amos, J. N., Takeuchi, N., Lill, A., Radford, J. Q., and Sunnucks, P. (2012). Fine-scale effects of habitat loss and fragmentation despite large-scale gene flow for some regionally declining woodland bird species. Landscape Ecology 27, 813–827.
Fine-scale effects of habitat loss and fragmentation despite large-scale gene flow for some regionally declining woodland bird species.Crossref | GoogleScholarGoogle Scholar |

Harrisson, K. A., Pavlova, A., Amos, J. N., Takeuchi, N., Lill, A., Radford, J. Q., and Sunnucks, P. (2013). Disrupted fine-scale population processes in fragmented landscapes despite large-scale genetic connectivity for a widespread and common cooperative breeder: the Superb Fairy-wren (Malurus cyaneus). Journal of Animal Ecology 82, 322–333.
Disrupted fine-scale population processes in fragmented landscapes despite large-scale genetic connectivity for a widespread and common cooperative breeder: the Superb Fairy-wren (Malurus cyaneus).Crossref | GoogleScholarGoogle Scholar | 23190389PubMed |

Higgins, P. J., and Peter, J. M. (Eds) (2003). ‘Handbook of Australian, New Zealand and Antarctic Birds. Vol. 6: Pardalotes to Shrike-thrushes.’ (Oxford University Press: Melbourne, Vic.)

Jakobsson, M., and Rosenberg, N. A. (2007). Clumpp: a cluster matching and permutation program for dealing with label switching and multimodality in analysis of population structure. Bioinformatics 23, 1801–1806.
Clumpp: a cluster matching and permutation program for dealing with label switching and multimodality in analysis of population structure.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXpt1ahtbs%3D&md5=23aebd595d88029d93336fa8264796f7CAS | 17485429PubMed |

Jaquiéry, J., Guillaume, F., and Perrin, N. (2009). Predicting the deleterious effects of mutation load in fragmented populations. Conservation Biology 23, 207–218.
Predicting the deleterious effects of mutation load in fragmented populations.Crossref | GoogleScholarGoogle Scholar | 18847439PubMed |

Johnson, M. S., and Brown, J. L. (1980). Genetic variation among trait groups and apparent absence of close inbreeding in Grey-crowned Babblers. Behavioral Ecology and Sociobiology 7, 93–98.
Genetic variation among trait groups and apparent absence of close inbreeding in Grey-crowned Babblers.Crossref | GoogleScholarGoogle Scholar |

Kalinowski, S. T., Taper, M. L., and Marshall, T. C. (2007). Revising how the computer program cervus accommodates genotyping error increases success in paternity assignment. Molecular Ecology 16, 1099–1106.
Revising how the computer program cervus accommodates genotyping error increases success in paternity assignment.Crossref | GoogleScholarGoogle Scholar | 17305863PubMed |

Kawano, K. M., Eguchi, K., Ueda, K., and Noske, R. (2007). Development of microsatellite markers in the Grey-crowned Babbler (Pomatostomus temporalis). Molecular Ecology Notes 7, 501–502.
Development of microsatellite markers in the Grey-crowned Babbler (Pomatostomus temporalis).Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXntVyktbo%3D&md5=5111344b771cf063da8711c69d4b93a4CAS |

Keller, L. F., and Waller, D. M. (2002). Inbreeding effects in wild populations. Trends in Ecology & Evolution 17, 230–241.
Inbreeding effects in wild populations.Crossref | GoogleScholarGoogle Scholar |

King, B. R. (1980). Social organization and behaviour of the Grey-crowned Babbler Pomatostomus temporalis. Emu 80, 59–76.
Social organization and behaviour of the Grey-crowned Babbler Pomatostomus temporalis.Crossref | GoogleScholarGoogle Scholar |

Koenig, W. D., Pitelka, F. A., Carmen, W. J., Mumme, R. L., and Stanback, M. T. (1992). The evolution of delayed dispersal in cooperative breeders. Quarterly Review of Biology 67, 111–150.
The evolution of delayed dispersal in cooperative breeders.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK38zkt1OlsA%3D%3D&md5=065e3fc838d81c67122d563ccfd2ce79CAS | 1635976PubMed |

Lesica, P., and Allendorf, F. W. (1995). When are peripheral populations valuable for conservation? Conservation Biology 9, 753–760.
When are peripheral populations valuable for conservation?Crossref | GoogleScholarGoogle Scholar |

McGarigal, K., Cushman, S. A., and Ene, E. (2012). FRAGSTATS v4: spatial pattern analysis program for categorical and continuous maps. University of Massachusetts, Amherst. Available at http://www.umass.edu/landeco/research/fragstats/fragstats.html [Verified 25 May 2016].

Méndez, M., Vögeli, M., Tella, J. L., and Godoy, J. A. (2014). Joint effects of population size and isolation on genetic erosion in fragmented populations: finding fragmentation thresholds for management. Evolutionary Applications 7, 506–518.
Joint effects of population size and isolation on genetic erosion in fragmented populations: finding fragmentation thresholds for management.Crossref | GoogleScholarGoogle Scholar | 24822084PubMed |

Mills, L. S., and Allendorf, F. W. (1996). The one-migrant-per-generation rule in conservation and management. Conservation Biology 10, 1509–1518.
The one-migrant-per-generation rule in conservation and management.Crossref | GoogleScholarGoogle Scholar |

Nei, M., Maruyama, T., and Chakraborty, R. (1975). The bottleneck effect and genetic variability in populations. Evolution 29, 1–10.
The bottleneck effect and genetic variability in populations.Crossref | GoogleScholarGoogle Scholar |

Palstra, F. P., and Ruzzante, D. E. (2008). Genetic estimates of contemporary effective population size: what can they tell us about the importance of genetic stochasticity for wild population persistence? Molecular Ecology 17, 3428–3447.
Genetic estimates of contemporary effective population size: what can they tell us about the importance of genetic stochasticity for wild population persistence?Crossref | GoogleScholarGoogle Scholar | 19160474PubMed |

Parris, K., and Schneider, A. (2009). Impacts of traffic noise and traffic volume on birds of roadside habitats. Ecology and Society 14, 29–51.

Peakall, R., and Smouse, P. E. (2006). GenAlEx 6: genetic analysis in Excel. Population genetic software for teaching and research. Molecular Ecology Notes 6, 288–295.
GenAlEx 6: genetic analysis in Excel. Population genetic software for teaching and research.Crossref | GoogleScholarGoogle Scholar |

Radford, J. Q. (2008). Influence of landscape characteristics on the abundance of the Grey-crowned Babbler (Pomatostomus temporalis temporalis) in the Loddon Valley, northern Victoria. Report for the North Central Catchment Management Authority and Department of Sustainability and Environment, Bendigo, Vic.

Radford, J. Q., and Bennett, A. F. (2007). The relative importance of landscape properties for woodland birds in agricultural environments. Journal of Applied Ecology 44, 737–747.
The relative importance of landscape properties for woodland birds in agricultural environments.Crossref | GoogleScholarGoogle Scholar |

Raymond, M., and Rousset, F. (1995). Genepop (version 1.2): population genetics software for exact tests and ecumenicism. Journal of Heredity 86, 248–249.

Rice, W. R. (1989). Analyzing tables of statistical tests. Evolution 43, 223–225.
Analyzing tables of statistical tests.Crossref | GoogleScholarGoogle Scholar |

Robinson, D. (1993). Habitat requirements of a threatened grassy woodland bird, the Grey-crowned Babbler. Project No. 900. Victorian Department of Conservation and Natural Resources (DCNR) and National Estates Grant Program (Australia). DCNR, Melbourne.

Robinson, D. (2006). Is revegetation in the Sheep Pen Creek area, Victoria, improving Grey-crowned Babbler habitat? Ecological Management & Restoration 7, 93–104.
Is revegetation in the Sheep Pen Creek area, Victoria, improving Grey-crowned Babbler habitat?Crossref | GoogleScholarGoogle Scholar |

Robinson, D., and Traill, B. J. (1996). Conserving woodland birds in the wheat and sheep belts of southern Australia. RAOU Conservation Statement 10, Royal Australasian Ornithologists Union, Melbourne. Available at http://birdsaustralia.com.au/documents/OTHPUB-cons_wheatbelt_sm_1.pdf [Verified 20 April 2016].

Rosenberg, N. A. (2004). Distruct: a program for the graphical display of population structure. Molecular Ecology Notes 4, 137–138.
Distruct: a program for the graphical display of population structure.Crossref | GoogleScholarGoogle Scholar |

Smouse, P. E., and Peakall, R. (1999). Spatial autocorrelation analysis of individual multiallele and multilocus genetic structure. Heredity 82, 561–573.
Spatial autocorrelation analysis of individual multiallele and multilocus genetic structure.Crossref | GoogleScholarGoogle Scholar | 10383677PubMed |

Stevens, K. P., Holland, G. J., Clarke, R. H., Cooke, R., and Bennett, A. F. (2015). What determines habitat quality for a declining woodland bird in a fragmented environment: the Grey-crowned Babbler Pomatostomus temporalis, in south-eastern Australia? PLoS One 10, e0130738.
What determines habitat quality for a declining woodland bird in a fragmented environment: the Grey-crowned Babbler Pomatostomus temporalis, in south-eastern Australia?Crossref | GoogleScholarGoogle Scholar | 26098355PubMed |

Sunnucks, P. (2011). Towards modelling persistence of woodland birds: the role of genetics. Emu 111, 19–39.
Towards modelling persistence of woodland birds: the role of genetics.Crossref | GoogleScholarGoogle Scholar |

Taylor, A. C., Walker, F. M., Goldingay, R. L., Ball, T., and van der Ree, R. (2011). Degree of landscape fragmentation influences genetic isolation among populations of a gliding mammal. PLoS One 6, e26651.
Degree of landscape fragmentation influences genetic isolation among populations of a gliding mammal.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXhsVyqu7zJ&md5=d31499c24779426b210fe04b32f7d550CAS | 22053200PubMed |

Tzaros, C. (1995). Population monitoring of the Grey-crowned Babbler (Pomatostomus temporalis) in central Victoria. Department of Conservation and Natural Resources, Bendigo, Vic.

Tzaros, C. (2001). Field surveys and population monitoring of the Grey-crowned Babbler Pomatostomus temporalis in the Loddon and Murray Valley regions, north-west Victoria. Department of Natural Resources and Environment, Melbourne, Vic.

Van Houtan, K. S., Pimm, S. L., Halley, J. M., Bierregaard, R. O., and Lovejoy, T. E. (2007). Dispersal of Amazonian birds in continuous and fragmented forest. Ecology Letters 10, 219–229.
Dispersal of Amazonian birds in continuous and fragmented forest.Crossref | GoogleScholarGoogle Scholar | 17305805PubMed |

Vergara, P. M., Perez-Hernandez, C. G., Hahn, I. J., and Jimenez, J. E. (2013). Matrix composition and corridor function for Austral Thrushes in a fragmented temperate forest. Landscape Ecology 28, 121–133.
Matrix composition and corridor function for Austral Thrushes in a fragmented temperate forest.Crossref | GoogleScholarGoogle Scholar |

Vesk, P. A., Robinson, D., van der Ree, R., Wilson, C. M., Saywell, S., and McCarthy, M. A. (2015). Demographic effects of habitat restoration for the Grey-crowned Babbler Pomatostomus temporalis, in Victoria, Australia. PLoS One 10, e0130153.
Demographic effects of habitat restoration for the Grey-crowned Babbler Pomatostomus temporalis, in Victoria, Australia.Crossref | GoogleScholarGoogle Scholar | 26177497PubMed |

Volpe, N. L., Hadley, A. S., Robinson, W. D., and Betts, M. G. (2014). Functional connectivity experiments reflect routine movement behavior of a tropical hummingbird species. Ecological Applications 24, 2122–2131.
Functional connectivity experiments reflect routine movement behavior of a tropical hummingbird species.Crossref | GoogleScholarGoogle Scholar |

Wittmer, H. U., McLellan, B. N., Serrouya, R., and Apps, C. D. (2007). Changes in landscape composition influence the decline of a threatened woodland Caribou population. Journal of Animal Ecology 76, 568–579.
Changes in landscape composition influence the decline of a threatened woodland Caribou population.Crossref | GoogleScholarGoogle Scholar | 17439473PubMed |