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Agonistic behavioural asymmetry in two species of montane lizard that exhibit elevational replacement

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Abstract

Context

In montane systems, closely related species tend to segregate spatially along elevational gradients. The role of biotic interactions, relative to species physiological requirements, in maintaining these distribution patterns is an important question in spatial ecology. Theory suggests that the role of interspecific competition can be significant in the maintenance of elevation replacement distributions. Despite this, there has been limited work investigating factors beyond thermophysiology in determining ranges in temperate montane species.

Objectives and methods

We investigated agonistic (i.e. aggressive) behaviour in response to a simulated intruder (conspecific versus heterospecific 3D printed models) in two sister species of temperate montane lizard, Liopholis guthega and L. montana, from south-eastern Australia. The two species have similar thermal tolerances at an area of distributional overlap between 1600 and 1700 m above sea level, above which L. montana is replaced by the high elevation specialist L. guthega.

Results

We found that response to intruder stimuli differed between the two species, with the high elevation L. guthega actively biting both conspecific and heterospecific models, whereas the lower elevation L. montana, never attacked either model type. Our findings provide evidence of asymmetric agonistic response in the two montane reptile species.

Conclusions

These findings have important implications for understanding how biological interactions and behaviour, in addition to thermo-physiological data, might mediate landscape scale distribution patterns both now and as environments change in the future. More broadly, our results are not consistent with the widespread idea that low elevation species will inevitably ‘push’ higher elevation species out, as global warming erodes species’ thermal envelopes.

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Data will be deposited on Figshare upon acceptance of the manuscript.

References

  • Atkins Z, Clemann N, Schroder M, Chapple DG, Davis NE, Robinson WA, Wainer J, Robert KA (2018) Consistent temporal variation in the diet of an endangered alpine lizard across two south-eastern Australian sky-islands. Austral Ecol 43:339–351

    Google Scholar 

  • Barve S, Dhont AA (2017) Elevational replacement of two Himalayan titmice: interspecific competition or habitat preference? J Avian Biol 48:1189–1194

    Google Scholar 

  • Cadena CD, Loiselle BA (2007) Limits to elevational distributions in two species of emberizine finches: disentangling the role of interspecific competition, autoecology, and geographic variation in the environment. Ecography 30:491–504

    Google Scholar 

  • Caldwell AJ, While GM, Beeton NJ, Wapstra E (2015) Potential for thermal tolerance to mediate climate change effects on three members of a cool temperate lizard genus, Niveoscincus. J Therm Biol 52:14–23

    PubMed  Google Scholar 

  • Chapple DG (2003) Ecology, life-history, and behavior in the Australian scincid genus Egernia, with comments on the evolution of complex sociality in lizards. Herpetological Monographs 17:145–180

    Google Scholar 

  • Chapple DG, Tingley R, Mitchell NJ, Macdonald SL, Keogh JS, Shea GM, Bowles P, Cox NA, Woinarski JCZ (2019) The Action Plan for Australian Lizards and Snakes 2017. CSIRO Publishing, Clayton

    Google Scholar 

  • Chock RY, Shier DM, Grether GF (2018) Body size, not phylogenetic relationship or residency, drives interspecific dominance in a little pocket mouse community. Anim Behav 137:197–204

    Google Scholar 

  • Clemann, N., Hutchinson, M., Robertson, P., Chapple, D. C, Gillespie, G., Melville, J. & Michael, D. 2018a. Liopholis montana. The IUCN Red List of Threatened Species 2018: e.T109478522A109478529. Downloaded on 22 July 2018.

  • Clemann, N., Chapple, D. C, Hutchinson, M., Robertson, P., Gillespie, G., Michael, D. & Melville, J. 2018b. Liopholis guthega. The IUCN Red List of Threatened Species 2018: e.T109477953A109478444. Downloaded on 22 July 2018.

  • Diamond JM (1973) Distributional ecology of New Guinea birds. Science 179:759–769

    CAS  PubMed  Google Scholar 

  • Donnellan SC, Hutchinson MN, Dempsey P, Osborne WS (2002) Systematics of the Egernia whitii species group (Lacertilia: Scincidae) in south-eastern Australia. Australian Journal of Zoology 50:439–459

    Google Scholar 

  • Duckworth RA, Belloni V, Anderson SR (2015) Cycles of species replacement emerge from locally induced maternal effects on offspring behavior in a passerine bird. Science 347:875–877

    CAS  PubMed  Google Scholar 

  • Duckworth RA, Hallinger KK, Hall N, Potticary AL (2017) Switch to a novel breeding resource influences coexistence of two passerine birds. Frontiers in Ecology and Evolution 5:72

    Google Scholar 

  • Fan M, Teunissen N, Hall ML, Hidalgo Aranzamendi N, Kingma SA, Roast M, Delhey K, Peters A (2018) From ornament to armament or loss of function? Breeding plumage acquisition in a genetically monogamous bird. J Anim Ecol 87:1274–1285

    PubMed  Google Scholar 

  • Fischer J, Lindenmayer DB (2005) The sensitivity of lizards to elevation: A case study from south-eastern Australia. Divers Distrib 11:225–233

    Google Scholar 

  • Freeman BG (2016) Strong asymmetric interspecific aggression between two sympatric New Guinean robins. Ibis 158:75–81

    Google Scholar 

  • Freeman BG, Miller ET (2018) Why do crows attack ravens? The roles of predation threat, resource competition, and social behaviour. Auk 135:857–867

    Google Scholar 

  • Freeman BG, Montgomery G (2015) Interspecific aggression by the Swainson’s thrush (Catharus ustulatus) may limit the distribution of the threatened Bicknell’s thrush (Catharus bicknelli) in the Adirondack Mountains. Condor 118:169–178

    Google Scholar 

  • Gifford ME, Kozak KH (2012) Islands in the sky or squeezed at the top? Ecological causes of elevational range limits in montane salamanders. Ecography 35:193–203

    Google Scholar 

  • Graham CH, Carnaval AC, Cadena CD, Zamudio KR, Roberts TE, Parra JL, McCain CM, Bowie RCK, Moritz C, Baines SB, Schneider CJ, van der Wal J, Rahbek C, Kozak KH, Sanders NJ (2014) The origin and maintenance of montane diversity: integrating evolutionary and ecological processes. Ecography 37:711–719

    Google Scholar 

  • Green K, Mansergh I, Osborne W (1992) The fauna of the Australian Alps: conservation and management. Review Géographie Alpine 2:381–407

    Google Scholar 

  • Grether GF, Peiman KS, Tobias JA, Robinson BW (2017) Causes and Consequences of Behavioral Interference between Species. Trends Ecol Evol 32:760–772

    PubMed  Google Scholar 

  • Hennessy K, Whetton P, Smith I, Bathols J, Hutchinson M, Sharples J (2003) The impact of climate change on snow conditions in mainland Australia. Aspendale, Victoria: CSIRO Atmospheric Research. Jankowski, J. E., Robinson, S. K. and Levey, D. J. 2010. Squeezed at the top: interspecific aggression may constrain elevational ranges in tropical birds. Ecology 91:1877–1884

    Google Scholar 

  • Krosby M, Wilsey CB, McGuire JL, Duggan JM, Nogeire TM, Heinrichs JA, Tewksbury JJ, Lawler JJ (2015) Climate-induced range overlap among closely related species. Nature Climate Change 5:883–887

    Google Scholar 

  • Kryštufek B, Janžekovič F, Donev NR (2008) Elevational diversity of reptiles on two Dinaric mountains. Journal of Natural History 42:399–408

    Google Scholar 

  • Langkilde T, Shine R (2004) Competing for crevices: interspecific conflict influences retreat-site selection in montane lizards. Oecologia 140:684–691

    PubMed  Google Scholar 

  • Langkilde T, Shine R (2007) Interspecific conflict in lizards: Social dominance depends upon an individual’s species not its body size. Austral Ecol 32:869–877

    Google Scholar 

  • Langkilde T, Lance VA, Shine R (2005) Ecological consequences of agonistic interactions in lizards. Ecology 86:1650–1659

    Google Scholar 

  • Lehtonen TK, Sowersby W, Wong BBM (2015a) Heterospecific aggression bias towards a rarer colour morph. Proceedings of the Royal Society of London B 282:20151551

    Google Scholar 

  • Lehtonen TK, Sowersby W, Gagnon K, Wong BBM (2015b) Cichlid fish use coloration as a cue to assess the threat status of heterospecific intruders. Am Nat 186:547–552

    PubMed  Google Scholar 

  • Martin PR, Freshwater C, Ghalambor CK (2017) The outcomes of most aggressive interactions among closely related bird species are asymmetric. PeerJ 5:e2847

    PubMed  PubMed Central  Google Scholar 

  • McArthur RH (1972) Geographical ecology: patterns in the distribution of species. Harper and Row, New York

    Google Scholar 

  • McEvoy J, While GM, Sinn DL, Wapstra E (2013) The role of size and aggression in intrasexual male competition in a social lizard species, Egernia whitii. Behav Ecol Sociobiol 67:79–90

    Google Scholar 

  • McEvoy J, While GM, Jones SM, Wapstra E (2015) Examining the role of testosterone in mediating short-term aggressive responses to social stimuli in a; izard. PLoS ONE 10:e0125015

    PubMed  PubMed Central  Google Scholar 

  • Melville J (2002) Competition and character displacement in two species of scincid lizards. Ecol Lett 5:386–393

    Google Scholar 

  • Michael D, Lindenmayer D (2018) Rocky outcrops in Australia: ecology, conservation and management. CSIRO Publishing, Clayton South, Victoria

    Google Scholar 

  • Pasch B, Bolker BM, Phelps SM, Gaillard AEJM, Bronstein EJL (2013) Interspecific dominance via vocal interactions mediates altitudinal zonation in Neotropical singing mice. Am Nat 182:E161–E173

    PubMed  Google Scholar 

  • Pickering C (2007) Climate change and other threats in the Australian Alps. In: Taylor M, Figgis P (eds) Protected Areas: Buffering nature against climate change (18: 28). WWF Australia, Sydney

    Google Scholar 

  • R Development Core Team (2018) R: a language and environment for statistical computing. [Internet]. Vienna: R Foundation for Statistical Computing; 2018.

  • Sato CF, Wood JT, Schroder M, Green K, Michael DR, Lindenmayer DB (2014) The impacts of ski resorts on reptiles: a natural experiment. Anim Conserv 17:313–322

    Google Scholar 

  • Senior AF, Atkins Z, Clemann N, Gardner MG, Schroder M, While GM, Wong BBM, Chapple DG (2019) Variation in thermal biology of three closely related lizard species along an elevation gradient. Biol J Lin Soc 127:278–291

    Google Scholar 

  • Sinervo B, Mendez-De la Cruz F, Miles DB, Heulin B, Bastiaans E, Santa Cruz MV, Lara-Resendiz R, Martinez-Méndez N, Calderon-Espinosa ML, Mesa-Lázaro RN, Gadsden H, Avila LJ, Morando M, De la Riva IJ, Sepulveda PV, Rocha CFD, Ibargüengoytia N, Puntriano CA, Massot M, Lepetz V, Oksanen TA, Chapple DG, Bauer AM, Branch WR, Clobert J, Sites JW (2010) Erosion of lizard diversity by climate change and altered thermal niches. Science 328:894–899. https://doi.org/10.1126/science.1184695

    Article  CAS  PubMed  Google Scholar 

  • Strangas ML, Navas CA, Rodrigues MT, Carnaval AC (2019) Thermophysiology, microclimates, and species distributions of lizards in the mountains of the Brazilian Atlantic Forest. Ecography 42:354–364

    Google Scholar 

  • Teasdale LC, Stevens M, Stuart-Fox D (2013) Discrete colour polymorphism in the tawny dragon lizard (Ctenophorus decresii) and differences in signal conspicuousness among morphs. J Evol Biol 26:1035–1046

    CAS  PubMed  Google Scholar 

  • Terborgh J, Weske JS (1975) Th e role of competition in thedistribution of Andean birds. Ecology 56:562–576

    Google Scholar 

  • Titone V, Marsiglia F, Mangiacotti M, Sacchi R, Scali S, Zuffi MAL (2017) Better to be resident, larger or coloured? Experimental analysis on intraspecific aggression in the ruin lizard. J Zool 304:260–267

    Google Scholar 

  • Umbers KDL, Osborne L, Keogh SJ (2012) The effects of residency and body size on contest initiation and outcome in the territorial dragon Ctenophorus decresii. PLoS ONE 7:e47143

    CAS  PubMed  PubMed Central  Google Scholar 

  • Vervust B, Van Dongen S, Grbac I, Van Damme R (2009) The mystery of the missing toes: Extreme levels of natural mutilation in island lizard populations. Funct Ecol 23:996–1003

    Google Scholar 

  • While GM, Sinn DL, Wapstra E (2009a) Female aggression predicts mode of paternity acquisition in a social lizard. Proceedings of the Royal Society of London B 276:2021–2029

    Google Scholar 

  • While GM, Uller T, Wapstra E (2009b) Within population variation in social strategies characterize the social and mating system of an Australian lizard, Egernia whitii. Austral Ecol 34:938–949

    Google Scholar 

  • Yewers MS, Pryke S, Stuart-Fox D (2016) Behavioural differences across contexts may indicate morph-specific strategies in the lizard Ctenophorus decresii. Anim Behav 111:329–339

    Google Scholar 

  • Zuur AF, Hilbe J, Leno EN (2013) A Beginner’s guide to GLM and GLMM with R: a frequentist and Bayesian perspective for ecologists. Highland Statistics, Newburgh (UK)

    Google Scholar 

Download references

Acknowledgements

We acknowledge First Nations Australians of the Ngarigo and Wurundjeri, upon whose land this research was undertaken. For logistical support we thank Justin Adams, Laura Cook, Kaspar Delhey, Emily Drummond, Marie Fan, Mark Feeney, Katelyn Hamilton, Rob Hayes, Carolyn Kovach, Topi Lehtonen, Chantel McCubbin, Matt McCurry, Alex McQueen, Jane Melville, Michelle Quayle, Mellesa Schroder, Chris Senior, and Brook Sykes. Special thanks to George Madani and Lachlan Hall for their photographs. This work was supported by the Holsworth Research Endowment (grant awarded to AFS), and an Australian Research Council Discovery Project Grant (DP150102900, grant to DGC, MMG and GMW).

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AFS carried out fieldwork, lab experiments and data analysis, contributed to the design of the study and wrote the manuscript. BBMW, DGC, NC and ZSA contributed to the design of the study and drafting of the manuscript. MGG and GMW contributed to the drafting of the manuscript. All authors gave final approval for publication.

Corresponding author

Correspondence to David G. Chapple.

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Research was conducted in accordance with appropriate collection and research permits (New South Wales: SL101798) and was approved by the Monash University animal welfare committee (BSCI/2016/24).

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Senior, A.F., Chapple, D.G., Atkins, Z.S. et al. Agonistic behavioural asymmetry in two species of montane lizard that exhibit elevational replacement. Landscape Ecol 36, 863–876 (2021). https://doi.org/10.1007/s10980-020-01184-5

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