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Ritualised Dung Kicking by White Rhino Males Amplifies Olfactory Signals but Reduces Odour Duration

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An Author Correction to this article was published on 11 March 2019

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Abstract

Many mammals enhance their olfactory signals visually by depositing them in conspicuous locations such as well-travelled paths. It is also possible to enhance the odour itself through behaviours aimed at modifying odour emission rates. White rhinos defecate in communal middens. While defecating, territorial males kick sharply with their back feet which disperses their dung. Despite being a ubiquitous trait of territorial male white rhinos, the reason behind this behaviour is unclear. We hypothesised that the purpose of dung kicking was for olfactory signal amplification (OSA) in terms of an increased emission of volatile compounds (i.e. increased signal strength). Using dung collected from non-territorial adult males (because it is not possible to collect whole dung from territorial males), we show that the dispersal of male white rhino dung causes OSA by increasing the emission of hydrocarbon acids. The dung odour of territorial and non-territorial males differs only quantitatively, hence it is likely that the same emission patterns occur for territorial male dung odours following dung dispersal. The volatile compound indicating age of intact dung was toluene, but for dispersed dung it was acetophenone (similar to territorial male dung). Despite the benefits of OSA, dung dispersal carried a cost of decreased odour longevity. Thus, signal detectability is temporally reduced. However, territorial males likely counteract this by defecating in middens both before and during peak visitation times by other individuals (15:00–23:00). As a result, we suggest that dung kicking by territorial males amplifies signal strength, such that their dung odours are the most prominent and easily detectable by individuals visiting the middens. This would then better signal territorial ownership to both potential rivals and potential mates.

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Change history

  • 11 March 2019

    The original version of this article unfortunately contained some mistakes.

  • 11 March 2019

    The original version of this article unfortunately contained some mistakes.

References

  • Alberts AC (1992) Constraints on the design of chemical communication systems in terrestrial vertebrates. Am Nat 139:S62–S89

    Article  Google Scholar 

  • Amirav A, Dagan S (1997) A direct sample introduction device for mass spectrometry studies and gas chromatorgraphy mass spectrometry anlyses. Eur J Mass Spectrom 3:105–111

    Article  CAS  Google Scholar 

  • Andersen KF, Vulpius T (1999) Urinary volatile constituents of the lion, Panthera leo. Chem Senses 24:179–189

    Article  PubMed  CAS  Google Scholar 

  • Archie EA, Theis KR (2011) Animal behaviour meets microbial ecology. Anim Behav 82:425–436

    Article  Google Scholar 

  • Archunan G, Rajagopal T (2013) Detection of estrus in Indian blackbuck: Behavioural, hormonal and urinary volatiles evaluation. Gen Comp Endocrinol 181:156–166

    Article  PubMed  CAS  Google Scholar 

  • Asa CS (1993) Relative contributions of urine and anal-sac secretions in scent marks of large felids. Am Zool 33:167–172

    Article  Google Scholar 

  • Barja I, de Miguel FJ, Barcena F (2004) The importance of crossroads in faecal marking behaviour of the wolves (Canis lupus). Die Naturwissenschaften 91:489–492

    Article  PubMed  CAS  Google Scholar 

  • Barja I, de Miguel FJ, Bárcena F (2005) Faecal marking behaviour of Iberian wolf in different zones of their territory. Folia Zool 54:21–29

    Google Scholar 

  • Bartoń K (2013) MuMIn: multi-model inference. R package version 1.9.13. The Comprehensive R Archive Network (CRAN), Vienna

    Google Scholar 

  • Bossert WH (1968) Temporal patterning in olfactory communication. J Theor Biol 18:157–170

    Article  PubMed  CAS  Google Scholar 

  • Brachares JS, Arcese P (1999) Scent marking in a territorial African antelope: II. The economics of marking with faeces. Anim Behav 57:11–17

    Article  Google Scholar 

  • Burger BV, Viviers MZ, Bekker JPI, Le Roux M, Fish N, Fourie WB, Weibchen G (2008) Chemical characterization of territorial marking fluid of male Bengal tiger, Panthera tigris. J Chem Ecol 34:659–671

    Article  PubMed  CAS  Google Scholar 

  • Burnham KP, Anderson DR (1998) Model selection and inference: a practical information-theoretic approach. Springer-Verlag, New York

    Book  Google Scholar 

  • Cross HB, Zedrosser A, Nevin O, Rosell F (2014) Sex discrimination via anal gland secretion in a territorial monogamous mammal. Ethol 120:1044–1052

    Article  Google Scholar 

  • Elkinton JS, Cardé RT (1984) Odor dispersion. In: Bell WJ, Cardé RT (eds) Chemical ecology of insects. Springer US, Boston, pp 73–91. https://doi.org/10.1007/978-1-4899-3368-3_3

    Chapter  Google Scholar 

  • Estes RD (1991) The behavior guide to African mammals. Univ California Press, Berkeley

    Google Scholar 

  • Giotto N, Laurent A, Mohamed N, Prevot N, Gerard J-F (2008) Observations on the behaviour and ecology of a threatened and poorly known dwarf antelope: the Beira (Dorcatragus megalotis). Eur J Wildl Res 54:539–547

    Article  Google Scholar 

  • Gorman ML, Mills MGL (1984) Scent marking strategies in hyaenas (Mammalia). J Zool 202:535–547

    Article  Google Scholar 

  • Gosling LM, Roberts SC (2001) Scent-marking by male mammals: cheat-proof signals to competitors and mates. Adv Study Behav 30:169–217

    Article  Google Scholar 

  • Hayward MW, Hayward GJ (2010) Potential amplification of territorial advertisement markings by black-backed jackals (Canis mesomelas). Behaviour 147:979–992

    Article  Google Scholar 

  • Hillman-Smith AKK, Owen-Smith N, Anderson JL, Hall-Martin AJ, Selaladi JP (1986) Age estimation of the white rhinoceros (Ceratotherium simum). J Zool 210:355–379

    Article  Google Scholar 

  • Jordan NR, Manser MB, Mwanguhya F, Kyabulima S, Rüedi P, Cant MA (2011) Scent marking in wild banded mongooses: 1. Sex-specific scents and overmarking. Anim Behav 81:31–42

    Article  Google Scholar 

  • Karthikeyan K, Muniasamy S, SankarGanesh D, Achiraman S, Archunan G (2013) Faecal chemical cues in water buffalo that facilitate estrus detection. Anim Reprod Sci 138:163–167

    Article  PubMed  CAS  Google Scholar 

  • Lerdau M, Guenther A, Monson R (1997) Plant production and emission of volatile organic compounds. BioScience 47:373–383

    Article  Google Scholar 

  • Liaw A, Wiener M (2012) Classification and regression by randomForest. R News 2:18–22

    Google Scholar 

  • Marneweck C, Jürgens A, Shrader AM (2017a) Dung odours signal sex, age, territorial and oestrous state in white rhinos. Proc R Soc B Biol Sci 284:20162376

    Article  CAS  Google Scholar 

  • Marneweck C, Jürgens A, Shrader AM (2017b) Temporal variation of white rhino dung odours. J Chem Ecol 43:955–965

    Article  PubMed  CAS  Google Scholar 

  • Marneweck C, Jürgens A, Shrader AM (2018) The role of middens in white rhino olfactory communication. Anim Behav 140:7–18

    Article  Google Scholar 

  • Monfort A, Monfort N (1974) Notes sur l’écologie et le comportement des oribis (Ourebia ourebi, Zimmerman, 1783). Rev Ecol 28:169–208

    Google Scholar 

  • Müller-Schwarze D, Houlihan PW (1991) Pheromonal activity of single castoreum constituents in beaver, Castor canadensis. J Chem Ecol 17:715–734. https://doi.org/10.1007/BF00994195

    Article  PubMed  Google Scholar 

  • Nimmermark S, Gustafsson G (2005) Influence of temperature, humidity and ventilation rate on the release of odor and ammonia in a floor housing system for laying hens. Agric Eng Int 7:1–14

    Google Scholar 

  • Oksanen J et al. (2015) Vegan: community ecology package. R package version 22-1

  • Osbourn AE, Lanzotti V (2009) Plant-derived natural products: synthesis, function, and application. Springer, New York

    Book  Google Scholar 

  • Owen-Smith N (1971) Territoriality in the white rhinoceros (Ceratotherium simum) Burchell. Nature 231:294–296

    Article  PubMed  CAS  Google Scholar 

  • Owen-Smith N (1973) The behavioural ecology of the white rhinoceros. The University of Wisconsin

  • Owen-Smith N (1975) The social ethology of the white rhinoceros Ceratotherium simum (Burchell 1817). Z Tierpsychologie 38:337–384

    Article  Google Scholar 

  • Piñeiro A, Barja I (2012) The plant physical features selected by wildcats as signal posts: an economic approach to fecal marking. Die Naturwissenschaften 99:801–809

    Article  PubMed  CAS  Google Scholar 

  • Pinheiro J, Bates D, DebRoy S, Sarkar D, Team RC (2015) nlme: linear and nonlinear mixed effects model. R package version 3.1–117

  • Rachlow JL, Berkeley EV (1998) Correlates of male mating strategies in white rhinos (Ceratotherium simum). J Mammal 79:1317–1324. https://doi.org/10.2307/1383023

    Article  Google Scholar 

  • Sharpe LL (2015) Handstand scent marking: height matters to dwarf mongooses. Anim Behav 105:173–179

    Article  Google Scholar 

  • Skinner JD, Chimimba CT (2005) The mammals of the southern African sub-region. Cambridge University Press, Cambridge

    Book  Google Scholar 

  • Somers M, Rasa OAE, Apps PJ (1990) Marking behaviour and dominance in suni antelpe (Neotragus moschatus). Z Säugetierk 55:340–352

    Google Scholar 

  • Stoddart DM (1976) Mammalian odours and pheromones. Edward Arnold Ltd, London

    Google Scholar 

  • Team RC (2016) A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna

    Google Scholar 

  • Theis KR, Schmidt TM, Holekamp KE (2012) Evidence for a bacterial mechanism for group-specific social odors among hyenas. Sci Rep 2:615

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  • Tinley KL (1969) Dikdik Madoqua kirki in South West Africa: notes on distribution, ecology and behaviour. Madoqua 1:7–33

    Google Scholar 

  • Vogt K, Zimmermann F, Kolliker M, Breitenmoser U (2014) Scent-marking behaviour and social dynamics in a wild population of Eurasian lynx Lynx lynx. Behav Process 106:98–106

    Article  Google Scholar 

  • Walther FR (1990) Duikers and dwarf antelopes. In: Parker SP (ed) Grzimek’s encyclopedia of mammals, vol 5. McGraw-Hill, New York, pp 325–343

    Google Scholar 

  • White AM, Swaisgood RR, Zhang H (2002) The highs and lows of chemical communication in giant pandas (Ailuropoda melanoleuca): effect of scent deposition height on signal discrimination. Behav Ecol Sociobiol 51:519–529

    Article  Google Scholar 

  • Zielinski WJ, Vandenbergh JG (1993) Testosterone and competitive ability in male house mice, Mus musculus: laboratory and field studies. Anim Behav 45:873–891

    Article  Google Scholar 

Download references

Acknowledgements

We thank Dr. Adam Shuttleworth for processing GC-MS samples and Chris Kelly (WildlifeACT Fund) for use of camera traps.

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Correspondence to C. Marneweck.

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Marneweck, C., Jürgens, A. & Shrader, A.M. Ritualised Dung Kicking by White Rhino Males Amplifies Olfactory Signals but Reduces Odour Duration. J Chem Ecol 44, 875–885 (2018). https://doi.org/10.1007/s10886-018-0988-3

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  • DOI: https://doi.org/10.1007/s10886-018-0988-3

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