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Behavioral Ecology and Sociobiology

, Volume 62, Issue 9, pp 1377–1388 | Cite as

Phenotypic correlates and survival consequences of male mating success in lek-mating greater prairie-chickens (Tympanuchus cupido)

  • Jacqueline K. NookerEmail author
  • Brett K. Sandercock
Original Paper

Abstract

Female choice and male–male aggression are two modes of sexual selection that can lead to elaboration of male morphological and behavioral traits. In lek-mating species, male mating success is often strongly skewed, and it is puzzling why variation in male traits is still observed given directional female choice. If male traits correlated with reproductive success are honest signals of male quality, there may be survival costs associated with the expression of those traits. In this study, we examined whether morphological, behavioral, and territorial traits are correlated with male mating success and survival in the lek-mating greater prairie-chicken (Tympanuchus cupido). We introduce a novel application of multinomial discrete choice models for analysis of female mate choice behavior. We found that behavioral and territorial attributes showed 6.5 times more variability among males than morphological traits. Both display and aggressive behaviors were strong predictors of male mating success, suggesting that both female choice and male–male aggression were important in determining mating success among male greater prairie-chickens. Moreover, annual survival of male prairie-chickens was independent of mating success and male traits. Females appear to be choosing males based on behavioral traits where large variation exists between males (coefficient of variation >30%). Behavioral traits were the most important factor in determining mating success of male prairie-chickens, but the mechanism underlying this relationship is unknown. In the future, experimental manipulations of male hormones or parasite loads could bridge the proximate mechanisms and ultimate consequences of factors mediating male mating success in lek-mating grouse.

Keywords

Galliformes Life history trade-off Mate choice Reproduction Sexual selection 

Notes

Acknowledgments

We thank Thomas Loughin for statistical assistance. Robert M. Gibson, Timothy H. Parker, and two anonymous reviewers gave helpful comments on previous drafts of the manuscript. We thank the following organizations and people for allowing access to their prairie-chicken leks: Konza Prairie Biological Station, a property of The Nature Conservancy managed by the Division of Biology at Kansas State University; Rannells Flint Hills Prairie Preserve managed by Dr. Clenton Owensby in the Department of Agronomy at Kansas State University; and private lands owned by Grant Poole. Tom VanSlyke and Kenny Berg provided logistical support. We thank Tracey Adamson, Jeremy Baumgardt, Amanda Behnke, Jarrod Bowers, Tara Conkling, Seth Cutright, DeVaughn Fraser, Chris Frey, Kyle Gerstner, Chod Hedinger, ‘Hoogy’ Hoogheem, Nichole Lambrecht, and Kara Oberle for field assistance. Funding for field work included a First Award from Kansas NSF EPSCoR Grant, a research grant from the American Ornithologists’ Union, and an NSF Doctoral Dissertation Improvement Grant (DEB-0608477). J. K. Nooker and B. K. Sandercock were supported by the Konza Prairie NSF Long-Term Ecological Research Grant (DEB-0218210) and by the Division of Biology at Kansas State University. The research performed in the present study complied with the current laws of the countries in which they were performed and were conducted under the following permits: Scientific, Education, or Exhibition Wildlife Permit, Kansas Department of Wildlife and Parks (SC-118-2003, SC-068-2004, SC-078-2005, SC-072-2006), and Institutional Animal Care and Use Committee (Protocols 2079, 2351).

References

  1. Alatalo RV, Höglund J, Lundberg A (1991) Lekking in the black grouse—a test of male viability. Nature 352:155–156CrossRefGoogle Scholar
  2. Alatalo RV, Burke T, Dann J, Hanotte O, Höglund J, Lundberg A, Moss R, Rintamaki PT (1996a) Paternity, copulation disturbance and female choice in lekking black grouse. Anim Behav 52:861–873CrossRefGoogle Scholar
  3. Alatalo RV, Höglund J, Lundberg A, Rintamaki PT, Silverin B (1996b) Testosterone and male mating success on the black grouse leks. Proc R Soc B 263:1697–1702CrossRefGoogle Scholar
  4. Ballard WB Jr, Robel RJ (1974) Reproductive importance of dominant male greater prairie chickens. Auk 91:75–85Google Scholar
  5. Balmford A (1991) Mate choice on leks. Trends Ecol Evol 6:87–92CrossRefGoogle Scholar
  6. Beani L, Dessì-Fulgheri F (1995) Mate choice in the grey partridge, Perdix perdix: role of physical and behavioural male traits. Anim Behav 49:347–356CrossRefGoogle Scholar
  7. Bleiweiss R (1997) Covariation of sexual dichromatism and plumage colours in lekking and non-lekking birds: a comparative analysis. Evol Ecol 11:217–235CrossRefGoogle Scholar
  8. Bradbury JW (1981) The evolution of leks. In: Alexander RD, Tinkle DW (eds) Natural selection and social behavior. Blackwell Scientific, Oxford, pp 138–169Google Scholar
  9. Bradbury JW, Gibson RM (1983) Leks and mate choice. In: Bateson P (ed) Mate choice. Cambridge University Press, Cambridge, pp 109–138Google Scholar
  10. Bradbury JW, Vehrencamp SL, Gibson RM (1989) Dispersion of displaying male sage grouse I. Patterns of temporal variation. Behav Ecol Sociobiol 24:1–14CrossRefGoogle Scholar
  11. Burnham KP, Anderson DR (2002) Model selection and multimodel inference, 2nd edn. Springer, New York, NYGoogle Scholar
  12. Buskirk SW, Millspaugh JJ (2006) Metrics for studies of resource selection. J Wildlife Manage 70:358–366CrossRefGoogle Scholar
  13. Cooper AB, Millspaugh JJ (1999) The application of discrete choice models to wildlife resource selection studies. Ecology 80:566–575CrossRefGoogle Scholar
  14. Delaune M (2003) XTools, a package of tools useful in vector spatial analysis. http://arcscripts.esri.com/details.asp?dbid=11526
  15. Drovetski SV, Rohwer S, Mode NA (2006) Role of sexual and natural selection in evolution of body size and shape: a phylogenetic study of morphological radiation in grouse. J Evol Biol 19:1083–1091PubMedCrossRefGoogle Scholar
  16. Fiske P, Rintamäki P, Karvonen E (1998) Mating success in lekking males: a meta-analysis. Behav Ecol 9:328–338CrossRefGoogle Scholar
  17. Gibson RM (1996) Female choice in sage grouse: the roles of attraction and active comparison. Behav Ecol Sociobiol 39:55–59CrossRefGoogle Scholar
  18. Gibson RM, Bradbury JW (1985) Sexual selection in lekking sage grouse: phenotypic correlates of male mating success. Behav Ecol Sociobiol 18:117–123CrossRefGoogle Scholar
  19. Gibson RM, Bradbury JW, Vehrencamp SL (1991) Mate choice in lekking sage grouse revisited: the roles of vocal display, female site fidelity, and copying. Behav Ecol 2:165–180CrossRefGoogle Scholar
  20. Gratson MW, Gratson GK, Bergerud AT (1991) Male dominance and copulation disruption do not explain variance in male mating success on sharp-tailed grouse (Tympanuchus phasianellus) leks. Behaviour 118:187–213CrossRefGoogle Scholar
  21. Hagelin JC, Ligon JD (2001) Female quail prefer testosterone-mediated traits, rather than the ornate plumage of males. Anim Behav 61:465–476CrossRefGoogle Scholar
  22. Hagen CA, Pitman JC, Sandercock BK, Robel RJ, Applegate RD (2005) Age-specific variation in apparent survival rates of male lesser prairie-chickens. Condor 107:78–86CrossRefGoogle Scholar
  23. Hamerstrom FN, Hamerstrom F (1973) The prairie chicken in Wisconsin. Wisconsin Dept of Natural Resources. Technical Bulletin No. 64. Madison, WIGoogle Scholar
  24. Hill WL (1991) Correlates of male mating success in the ruff Philomachus pugnax, a lekking shorebird. Behav Ecol Sociobiol 29:367–372CrossRefGoogle Scholar
  25. Höglund J, Lundberg A (1987) Sexual selection in a monomorphic lek-breeding bird: correlates of male mating success in the great snipe Gallinago media. Behav Ecol Sociobiol 21:211–216CrossRefGoogle Scholar
  26. Höglund J, Alatalo RV (1995) Leks. Princeton University Press, Princeton, NJGoogle Scholar
  27. Höglund J, Alatalo RV, Lundberg A (1992a) The effects of parasites on male ornaments and female choice in the lek-breeding black grouse (Tetrao tetrix). Behav Ecol Sociobiol 30:71–76CrossRefGoogle Scholar
  28. Höglund J, Kålås JA, Fiske P (1992b) The costs of secondary sexual characteristics in the lekking great snipe (Gallinago media). Behav Ecol Sociobiol 30:309–315CrossRefGoogle Scholar
  29. Höglund J, Johansson T, Pelabon C (1997) Behaviourally mediated sexual selection: characteristics of successful male black grouse. Anim Behav 54:255–264CrossRefGoogle Scholar
  30. Hooge PN, Eichenlaub W, Solomon W (1999) The Animal Movement Program. USGS. Alaska Biological Science Center. http://www.absc.usgs.gov/glba/gistools/index.htm
  31. Hurlbert SH (1984) Pseudoreplication and the design of ecological field experiments. Ecol Monogr 54:187–211CrossRefGoogle Scholar
  32. Jennions MD, Møller AP, Petrie M (2001) Sexually selected traits and adult survival: a meta-analysis. Q Rev Biol 76:3–36PubMedCrossRefGoogle Scholar
  33. Kaiser HF (1960) The application of electronic computers to factor analysis. Educ Psychol Meas 20:141–151CrossRefGoogle Scholar
  34. Kimball RT, Ligon JD (1999) Evolution of avian plumage dichromatism from a proximate perspective. Am Nat 154:182–193CrossRefGoogle Scholar
  35. Kokko H, Lindström J (1997) Measuring the mating skew. Am Nat 149:794–799CrossRefGoogle Scholar
  36. Moore JE, Swihart RK (2006) Nut selection by captive blue jays: importance of availability and implications for seed dispersal. Condor 108:377–388CrossRefGoogle Scholar
  37. Mougeot F, Irvine JR, Seivwright L, Redpath SM, Piertney S (2004) Testosterone, immunocompetence, and honest sexual signaling in male red grouse. Behav Ecol 15:930–937CrossRefGoogle Scholar
  38. Nonacs P (2000) Measuring and using skew in the study of social behavior and evolution. Am Nat 156:577–589CrossRefGoogle Scholar
  39. Nooker JK (2007) Factors affecting the demography of a lek-mating bird: The greater prairie-chicken. Ph.D. Dissertation. Kansas State UniversityGoogle Scholar
  40. Parker TH, Ligon JD (2003) Female mating preferences in red junglefowl: a meta-analysis. Ethol Ecol Evol 15:63–72CrossRefGoogle Scholar
  41. Redpath SM, Mougeot F, Leckie FM, Evans SA (2006) The effects of autumn testosterone on survival and productivity in red grouse, Lagopus lagopus scoticus. Anim Behav 71:1297–1305CrossRefGoogle Scholar
  42. Reynolds JD, Gross MR (1990) Costs and benefits of female mate choice: is there a lek paradox? Am Nat 136:230–243CrossRefGoogle Scholar
  43. Rintamäki PT, Lundberg A, Alatalo RV, Höglund J (1998) Assortative mating and female clutch investment in black grouse. Anim Behav 56:1399–1403PubMedCrossRefGoogle Scholar
  44. Rintamäki PT, Höglund J, Karvonen E, Alatalo RV, Björklund N, Lundberg A, Rätti O, Vouti J (2000) Combs and sexual selection in black grouse (Tetrao tetrix). Behav Ecol 11:465–471CrossRefGoogle Scholar
  45. Robel RJ (1966) Booming territory size and mating success of the greater prairie chicken (Tympanuchus cupido pinnatus). Anim Behav 14:328–331PubMedCrossRefGoogle Scholar
  46. Robel RJ (1970) Possible role of behavior in regulating greater prairie-chicken populations. J Wildlife Manage 34:306–312CrossRefGoogle Scholar
  47. Robel RJ, Ballard WB Jr (1974) Lek social organization and reproductive success in the greater prairie chicken. Am Zool 14:121–128Google Scholar
  48. Sæther SA, Fiske P, Kålås JA (1999) Pushy males and choosy females: courtship disruption and mate choice in the lekking great snipe. Proc R Soc Lond B 266:1227–1234CrossRefGoogle Scholar
  49. Sæther SA, Fiske P, Kålås JA (2001) Male mate choice, sexual conflict and strategic allocation of copulations in a lekking bird. Proc R Soc Lond B 268:2097–2102CrossRefGoogle Scholar
  50. Sæther SA, Baglo R, Fiske P, Ekblom R, Höglund J, Kålås JA (2005) Direct and indirect mate choice on leks. Am Nat 166:145–157PubMedCrossRefGoogle Scholar
  51. Sandercock BK (2006) Estimation of demographic parameters from live-encounter data: a summary review. J Wildlife Manage 70:1504–1520CrossRefGoogle Scholar
  52. SAS Institute (2003) SAS User’s Guide: Statistics, ver. 9. SAS Institute, Cary, North Carolina, USAGoogle Scholar
  53. Schroeder MA, Robb LA (1993). Greater prairie-chicken (Tympanuchus cupido). In: Poole A, Stettenheim P, Gill F (eds) The birds of North America. No. 36. The American Ornithologists’ Union and the Academy of Natural Sciences of PhiladelphiaGoogle Scholar
  54. Seivwright LJ, Redpath SM, Mougeot F, Leckie F, Hudson PJ (2005) Interactions between intrinsic and extrinsic mechanisms in a cyclic species: testosterone increases parasite infection in red grouse. Proc R Soc Lond B 272:2299–2304CrossRefGoogle Scholar
  55. Semple K, Wayne RK, Gibson RM (2001) Microsatellite analysis of female mating behaviour in lek-breeding sage grouse. Mol Ecol 10:2043–2048PubMedCrossRefGoogle Scholar
  56. Shorey L (2002) Mating success on white-bearded manakin (Manacus manacus) leks: male characteristics and relatedness. Behav Ecol Sociobiol 52:451–457CrossRefGoogle Scholar
  57. Spurrier MF, Boyce MS, Manly BF (1994) Lek behaviour in captive sage grouse Centrocercus urophasianus. Anim Behav 47:303–310CrossRefGoogle Scholar
  58. Toepfer JE, Newell JA, Monarch J (1987) A method for trapping prairie grouse hens on display grounds. Contribution No. 2144, Montana Agricultural Experimental StationGoogle Scholar
  59. Vehrencamp SL, Bradbury JW, Gibson RM (1989) The energetic cost of display in male sage grouse. Anim Behav 38:885–896CrossRefGoogle Scholar
  60. West PM, Packer C (2002) Sexual selection, temperature and the lion’s mane. Science 297:1339–1343PubMedCrossRefGoogle Scholar
  61. Wiley RH (1991) Lekking in birds and mammals: behavioral and evolutionary issues. Adv Stud Behav 20:201–291CrossRefGoogle Scholar
  62. Zuk M, Johnsen TS, Maclarty T (1995a) Endocrine-immune interactions, ornaments and mate choice in red jungle fowl. Proc R Soc Lond B 260:205–210CrossRefGoogle Scholar
  63. Zuk M, Popma SL, Johnsen TS (1995b) Male courtship displays, ornaments and female mate choice in captive red jungle fowl. Behaviour 132:821–836CrossRefGoogle Scholar

Copyright information

© Springer-Verlag 2008

Authors and Affiliations

  1. 1.Division of BiologyKansas State UniversityManhattanUSA
  2. 2.Department of BiologyWartburg CollegeWaverlyUSA

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