Skip to main content
Log in

Queuing in space and time reduces the lek paradox on an antelope lek

  • Original Paper
  • Published:
Evolutionary Ecology Aims and scope Submit manuscript

Abstract

Lek systems, where females often use centrality to assess male quality, highlight a general paradox in evolutionary biology: how can female preferences for males providing good genes persist when consequential strong directional selection is predicted to deplete additive genetic variance in male quality and thereby obliterate benefits of choosiness? An explanation contributing to the resolution of this lek paradox may be that genetic variance is retained when an indirect mate choice cue, such as centrality on a lek, is an imperfect indicator of male genetic quality. Here I investigate whether the presence of alternative male mating tactics limits the reliability of centrality as a quality indicator in lek-breeding topi antelopes. Whereas males establishing territories directly on the central lek were relatively large, smaller peripheral males regularly shifted their territories centripetally and in this way also occasionally obtained central territories. By such opportunistic queuing, small males could increase their mating success drastically; however, their territorial tenure in the lek centre was relatively short, consistent with moderate competitive ability. These results suggest that male topi antelopes can obtain central lek territories through alternative mating tactics, providing scope for variance in male quality on the central lek. In a separate finding, the mating success of central males was found to increase during territorial tenure, independent of estimated age. The demonstration of queuing in both space and time on a mammalian lek highlights the importance of considering male tactical dynamics over time in order to avoid an inflated appearance of the lek paradox.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  • Ahnesjö I, Kvarnemo C, Merilaita S (2001) Using potential reproductive rates to predict mating competition among individuals qualified to mate. Behav Ecol 12:397–401

    Article  Google Scholar 

  • Anthony AJ, Lightfoot CJ (1984) Field determination of age and sex in tsessebe Damaliscus lunatus. S Afr J Wildl Res 14:19–22

    Google Scholar 

  • Apollonio M, Festa-Bianchet M, Mari F, Riva M (1990) Site-specific asymmetries in male copulatory success in a fallow deer lek. Anim Behav 39:205–212

    Article  Google Scholar 

  • Apollonio M, Festa-Bianchet M, Mari F, Mattioli S, Sarno B (1992) To lek or not to lek—mating strategies of male fallow deer. Behav Ecol 3:25–31

    Article  Google Scholar 

  • Bakker TCM, Pomiankowski A (1995) The genetic basis of female mate preferences. J Evol Biol 8:129–171

    Article  Google Scholar 

  • Balmford A (1990) Lekking in Uganda kob. PhD thesis, University of Cambridge

  • Balmford A, Albon S, Blakeman S (1992) Correlates of male mating success and female choice in a lek-breeding antelope. Behav Ecol 3:112–123

    Article  Google Scholar 

  • Beehler BM, Foster MS (1988) Hotshots, hotspots, and female preference in the organization of lek mating systems. Am Nat 131:203–219

    Article  Google Scholar 

  • Bercovitch FB, Loomis CP, Rieches RG (2009) Age-specific changes in reproductive effort and terminal investment in female Nile lechwe. J Mammal 90:40–46

    Article  Google Scholar 

  • Borgia G (1979) Sexual selection and the evolution of mating systems. In: Blum MS, Blum NA (eds) Sexual selection and reproductive competition. Academic Press, New York, pp 19–80

    Google Scholar 

  • Bradbury JW (1981) The evolution of leks. In: Alexander RD, Tinkle DW (eds) Natural selection and social behaviour. Chiron Press, New York, pp 138–169

    Google Scholar 

  • Bradbury JW, Vehrencamp SL (1998) Principles of animal communication. Sinauer, Sunderland

    Google Scholar 

  • Bro-Jørgensen J (2001) Lek-breeding in topi antelopes (Damaliscus lunatus). PhD thesis, University of London

  • Bro-Jørgensen J (2002) Overt female mate competition and preference for central males in a lekking antelope. Proc Natl Acad Sci USA 99:9290–9293

    Article  PubMed  Google Scholar 

  • Bro-Jørgensen J (2003) No peace for estrous topi cows on leks. Behav Ecol 14:521–525

    Article  Google Scholar 

  • Bro-Jørgensen J (2007a) The intensity of sexual selection predicts weapon size in male bovids. Evolution 61:1316–1326

    Article  PubMed  Google Scholar 

  • Bro-Jørgensen J (2007b) Reversed sexual conflict in a promiscuous antelope. Curr Biol 17:2157–2161

    Article  PubMed  Google Scholar 

  • Bro-Jørgensen J (2008) The impact of lekking on the spatial variation in payoffs to resource-defending topi bulls (Damaliscus lunatus). Anim Behav 75:1229–1234

    Article  Google Scholar 

  • Bro-Jørgensen J (2011) Intra- and intersexual conflicts and cooperation in the evolution of mating strategies: lessons learnt from ungulates. Evol Biol 38:28–41

    Article  Google Scholar 

  • Bro-Jørgensen J, Durant SM (2003) Mating strategies of topi bulls: getting in the centre of attention. Anim Behav 65:585–594

    Article  Google Scholar 

  • Byers JA, Waits L (2006) Good genes sexual selection in nature. Proc Natl Acad Sci USA 103:16343–16345

    Article  PubMed  CAS  Google Scholar 

  • Clutton-Brock TH, Guinness FE, Albon SD (1982) Red deer—behaviour and ecology of two sexes. Edinburgh University Press, Edinburgh

    Google Scholar 

  • Clutton-Brock TH, Hiraiwa-Hasegawa M, Robertson A (1989) Mate choice on fallow deer leks. Nature 340:463–465

    Article  PubMed  CAS  Google Scholar 

  • Cornwallis CK, Uller T (2010) Towards an evolutionary ecology of sexual traits. Trends Ecol Evol 25:145–152

    Article  PubMed  Google Scholar 

  • East ML, Hofer H (2001) Male spotted hyenas (Crocuta crocuta) queue for status in social groups dominated by females. Behav Ecol 12:558–568

    Article  Google Scholar 

  • East ML, Burke T, Wilhelm K, Greig C, Hofer H (2003) Sexual conflicts in spotted hyenas: male and female mating tactics and their reproductive outcome with respect to age, social status and tenure. Proc R Soc Lond B 270:1247–1254

    Article  Google Scholar 

  • Falconer DS (1981) Introduction to quantitative genetics, 2nd edn. Longman, London

    Google Scholar 

  • Gosling LM, Petrie M (1990) Lekking in topi: a consequence of satellite behavior by small males at hotspots. Anim Behav 40:272–287

    Article  Google Scholar 

  • Hall MD, Lailvaux SP, Blows MW, Brooks RC (2010) Sexual conflict and the maintenance of multivariate genetic variation. Evolution 64:1697–1703

    Article  PubMed  Google Scholar 

  • Höglund J, Alatalo RV (1995) Leks. Princeton University Press, Princeton, New Jersey

    Google Scholar 

  • Höglund J, Robertson JGM (1990) Female preferences, male decision rules and the evolution of leks in the great snipe (Gallinago media). Anim Behav 40:15–22

    Article  Google Scholar 

  • Hunt J, Bussiere LF, Jennions MD, Brooks R (2004) What is genetic quality? Trends Ecol Evol 19:329–333

    Article  PubMed  Google Scholar 

  • Isvaran K, Jhala Y (2000) Variation in lekking costs in blackbuck (Antilope cervicapra): relationship to lek-territory location and female mating patterns. Behaviour 137:547–563

    Article  Google Scholar 

  • Jewell PA (1972) Social organisation and movements of topi (Damaliscus korrigum) during the rut, at Ishasha, Queen Elizabeth Park, Uganda. Zool Afr 7:233–255

    Google Scholar 

  • Johnson T, Barton N (2005) Theoretical models of selection and mutation on quantitative traits. Philos Trans R Soc B 360:1411–1425

    Article  CAS  Google Scholar 

  • Kokko H, Johnstone RA (1999) Social queuing in animal societies: a dynamic model of reproductive skew. Proc R Soc Lond B 266:571–578

    Article  Google Scholar 

  • Kokko H, Lindström J, Alatalo RV, Rintamäki PT (1998) Queuing for territory positions in the lekking black grouse (Tetrao tetrix). Behav Ecol 9:376–383

    Article  Google Scholar 

  • Kotiaho JS, Simmons LW, Tomkins JL (2001) Towards a resolution of the lek paradox. Nature 410:684–686

    Article  PubMed  CAS  Google Scholar 

  • Kotiaho JS, Lebas NR, Puurtinen M, Tomkins JL (2008) On the resolution of the lek paradox. Trends Ecol Evol 23:1–3

    Article  PubMed  Google Scholar 

  • McElligott AG, Altwegg R, Hayden TJ (2002) Age-specific survival and reproductive probabilities: evidence for senescence in male fallow deer (Dama dama). Proc R Soc Lond B 269:1129–1137

    Article  Google Scholar 

  • Nefdt RJC (1992) Lek-breeding in Kafue lechwe. PhD thesis, University of Cambridge

  • Nefdt RJC, Thirgood SJ (1997) Lekking, resource defense, and harassment in two subspecies of lechwe antelope. Behav Ecol 8:1–9

    Article  Google Scholar 

  • Nussey DH, Kruuk LEB, Morris A, Clements MN, Pemberton JM, Clutton-Brock TH (2009) Inter- and intrasexual variation in aging patterns across reproductive traits in a wild red deer population. Am Nat 174:342–357

    Article  PubMed  Google Scholar 

  • Pelletier F, Festa-Bianchet M (2006) Sexual selection and social rank in bighorn rams. Anim Behav 71:649–655

    Article  Google Scholar 

  • Petrie M, Roberts G (2007) Sexual selection and the evolution of evolvability. Heredity 98:198–205

    Article  PubMed  CAS  Google Scholar 

  • Pomiankowski A, Møller AP (1995) A resolution of the lek paradox. Proc R Soc Lond B 260:21–29

    Article  Google Scholar 

  • Radwan J (2008) Maintenance of genetic variation in sexual ornaments: a review of the mechanisms. Genetica 134:113–127

    Article  PubMed  Google Scholar 

  • Saether SA, Baglo R, Fiske P, Ekblom R, Höglund J, Kålås A (2005) Direct and indirect mate choice on leks. Am Nat 166:145–157

    Article  PubMed  Google Scholar 

  • Stearns SC (1992) The evolution of life histories. Oxford University Press, Oxford

    Google Scholar 

  • Tomkins JL, Radwan J, Kotiaho JS, Tregenza T (2004) Genic capture and resolving the lek paradox. Trends Ecol Evol 19:323–328

    Article  PubMed  Google Scholar 

  • Wade MJ (1979) Sexual selection and variance in reproductive success. Am Nat 114:742–764

    Article  Google Scholar 

  • Weckerly FW (1998) Sexual-size dimorphism: influence of mass and mating systems in the most dimorphic mammals. J Mammal 79:33–52

    Article  Google Scholar 

  • Wiley RH, Poston J (1996) Perspective: indirect mate choice, competition for mates, and coevolution of the sexes. Evolution 50:1371–1381

    Article  Google Scholar 

  • Wilson AJ, Nussey DH (2010) What is individual quality? An evolutionary perspective. Trends Ecol Evol 25:207–214

    Article  PubMed  Google Scholar 

  • Wilson AJ, Kruuk LEB, Coltman DW (2005) Ontogenetic patterns in heritable variation for body size: using random regression models in a wild ungulate population. Am Nat 166:E177–E192

    Article  PubMed  Google Scholar 

Download references

Acknowledgments

I thank the Ministry of Science and Technology in Kenya, Narok County Council, the Senior Warden of Masai Mara National Reserve, the Management of the Olare Orok Conservancy and Kenya Wildlife Service for permission to do field work, Mada Hotels (T. Mhajan) for logistic support, and Simone Ciuti and two anonymous reviewers for valuable comments. This research was supported by Marie Curie, ZSL and RCUK fellowships to the author.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Jakob Bro-Jørgensen.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Bro-Jørgensen, J. Queuing in space and time reduces the lek paradox on an antelope lek. Evol Ecol 25, 1385–1395 (2011). https://doi.org/10.1007/s10682-011-9523-5

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10682-011-9523-5

Keywords

Navigation