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Behavioral Ecology and Sociobiology

, Volume 64, Issue 2, pp 169–182 | Cite as

Light environment and mating behavior in Trinidadian guppies (Poecilia reticulata)

  • Gabrielle A. ArchardEmail author
  • Innes C. Cuthill
  • Julian C. Partridge
Original Paper

Abstract

Male guppies, Poecilia reticulata, have color patterns that result from a balance between natural selection for crypsis to avoid predators and sexual selection for bright, complex patterns that attract females. Males use displays to show off these patterns to potential mates, but their conspicuousness also depends on the light environment in which they are viewed. We investigated variation in natural underwater guppy light environments in Trinidad, West Indies, and found that mating behavior is correlated with both the ‘quantity’ (total irradiance) and ‘quality’ (spectral composition) of light: light intensity and the proportion of ultraviolet light were negatively related to display rates. Experimental manipulation of light environment to mimic natural daily changes demonstrated that these relationships are causal and are independent of time of day effects. At lower light levels, when guppies are less detectable by visually hunting predators, females had more opportunity for active mate choice, because males displayed more. However, these light conditions may reduce the ability of females to accurately discriminate between males. Guppy mating behavior is therefore strongly affected by light environment, and this may have important effects on sexual selection.

Keywords

Guppy Light environment Irradiance Mating behavior Sexual selection 

Notes

Acknowledgements

GAA was funded by a Natural Environment Research Council, UK, Ph.D. Studentship (NERC/S/A/2002/10321). This work was carried out using equipment bought from a Biotechnology and Biological Sciences Research Council grant (7/S18903), to ICC, JCP, and Dr. T. Troscianko. Thanks to Mark Priest, Prof. Anne Warren, and Andrew Mead for assistance in the field. The Water and Sewerage Authority of Trinidad and Tobago gave permission for the work in the Quare River at the Hollis Reservoir. We thank Prof. John Endler, Prof. Justin Marshall, Dr. Sami Merilaita, and four anonymous referees for their valuable comments on earlier versions of the manuscript. All fieldwork and experiments described in this study complied with the laws of Trinidad and Tobago at the time of the study.

Supplementary material

265_2009_834_MOESM1_ESM.doc (45 kb)
ESM S1 (DOC 46 kb)

References

  1. Archard GA (2006) Context-dependent mating behaviour in the guppy, Poecilia reticulata. PhD dissertation. University of Bristol, BristolGoogle Scholar
  2. Buck J (1988) Synchronous rhythmic flashing of fireflies. II. Q Rev Biol 63:265–289. doi: 10.1086/415929 CrossRefPubMedGoogle Scholar
  3. Chiao C-C, Osorio D, Vorobyev M, Cronin TW (2000) Characterization of natural illuminants in forests and the use of digital video data to reconstruct illuminant spectra. J Opt Soc Am A 17:1713–1721. doi: 10.1364/JOSAA.17.001713 CrossRefGoogle Scholar
  4. Crawley M (2002) Statistical computing: an introduction to data analysis using S-plus. Wiley, ChichesterGoogle Scholar
  5. Cuthill IC, Bennett ATD, Partridge JC, Maier EH (1999) Plumage reflectance and the objective assessment of avian sexual dichromatism. Am Nat 153:183–200. doi: 10.1086/303160 CrossRefGoogle Scholar
  6. Douglas RH, Hawryshyn CW (1990) Behavioral studies of fish vision: an analysis of visual capabilities. In: Douglas RH, Djamgoz MBA (eds) The visual system of fish. Chapman and Hall, London, pp 373–418Google Scholar
  7. Endler JA (1987) Predation, light intensity and courtship behavior in Poecilia reticulata (Pisces: Poeciliidae). Anim Behav 35:1376–1385. doi: 10.1016/S0003-3472(87)80010-6 CrossRefGoogle Scholar
  8. Endler JA (1990) On the measurement and classification of colour in studies of animal colour patterns. Biol J Linn Soc 41:315–352CrossRefGoogle Scholar
  9. Endler JA (1991) Variation in the appearance of guppy color patterns to guppies and their predators under different visual conditions. Vision Res 31:587–608. doi: 10.1016/0042-6989(91)90109-I CrossRefPubMedGoogle Scholar
  10. Endler JA (1992) Signals, signal conditions, and the direction of evolution. Am Nat 139:S125–S153. doi: 10.1086/285308 CrossRefGoogle Scholar
  11. Endler JA (1993) The color of light in forests and its implications. Ecol Monogr 63:1–27CrossRefGoogle Scholar
  12. Endler JA (1995) Multiple-trait coevolution and environmental gradients in guppies. Trends Ecol Evol 10:22–29. doi: 10.1016/S0169-5347(00)88956-9 CrossRefGoogle Scholar
  13. Endler JA, Houde AE (1995) Geographic variation in female preferences for male traits in Poecilia reticulata. Evolution 49:456–468CrossRefGoogle Scholar
  14. Endler JA, Théry M (1996) Interacting effects of lek placement, display behavior, ambient light, and color patterns in three neotropical forest-dwelling birds. Am Nat 148:421–452. doi: 10.1086/285934 CrossRefGoogle Scholar
  15. Farr JA (1980) Social behavior patterns as determinants of reproductive success in the guppy, Poecilia reticulata Peters (Pisces: Poeciliidae): an experimental study of the effects of inter-male competition, female choice, and sexual selection. Behaviour 74:38–91. doi: 10.1163/156853980X00311 CrossRefGoogle Scholar
  16. Forsman A, Appelqvist S (1998) Visual predators impose correlational selection on prey color, pattern and behavior. Behav Ecol 9:409–413. doi: 10.1093/beheco/9.4.409 CrossRefGoogle Scholar
  17. Fuller RC (2002) Lighting environment predicts the relative abundance of male colour morphs in bluefin killifish (Lucania goodei) populations. Proc R Soc Lond B Biol Sci 269:1457–1465. doi: 10.1098/rspb.2002.2042 CrossRefGoogle Scholar
  18. Godin JGJ, Briggs SE (1996) Female mate choice under predation risk in the guppy. Anim Behav 51:117–130. doi: 10.1006/anbe.1996.0010 CrossRefGoogle Scholar
  19. Gong A (1997) The effects of predator exposure on the female choice of guppies (Poecilia reticulata) from a high-predation population. Behaviour 134:373–389. doi: 10.1163/156853997X00593 CrossRefGoogle Scholar
  20. Gong A, Gibson RM (1996) Reversal of female preference after visual exposure to a predator in the guppy, Poecilia reticulata. Anim Behav 52:1007–1017. doi: 10.1006/anbe.1996.0248 CrossRefGoogle Scholar
  21. Grether GF, Hudon J, Millie DF (1999) Carotenoid limitation of sexual colouration along an environmental gradient in guppies. Proc R Soc Lond B Biol Sci 266:1317–1322. doi: 10.1098/rspb.1999.0781 CrossRefGoogle Scholar
  22. Houde AE, Torio AJ (1992) Effect of parasitic infection on male color pattern and female choice in guppies. Behav Ecol 3:346–351. doi: 10.1093/beheco/3.4.346 CrossRefGoogle Scholar
  23. Kodric-Brown A (1993) Female choice of multiple male criteria in guppies—interacting effects of dominance, coloration and courtship. Behav Ecol Sociobiol 32:415–420. doi: 10.1007/BF00168825 Google Scholar
  24. Long KD, Rosenqvist G (1998) Changes in male guppy courting distance in response to a fluctuating light environment. Behav Ecol Sociobiol 44:77–83. doi: 10.1007/s002650050518 CrossRefGoogle Scholar
  25. López S (1998) Acquired resistance affects male sexual display and female choice in guppies. Proc R Soc Lond B Biol Sci 265:717–723. doi: 10.1098/rspb.1998.0352 CrossRefGoogle Scholar
  26. Lythgoe JN (1979) The ecology of vision. Clarendon, OxfordGoogle Scholar
  27. Magellan K, Pettersson LB, Magurran AE (2005) Quantifying male attractiveness through phenotypic size manipulation in the Trinidadian guppy, Poecilia reticulata. Behav Ecol Sociobiol 58:366–374. doi: 10.1007/s00265-005-0950-6 CrossRefGoogle Scholar
  28. Magurran AE, Seghers BH (1994) A cost of sexual harassment in the guppy, Poecilia reticulata. Proc R Soc Lond B Biol Sci 258:89–92. doi: 10.1098/rspb.1994.0147 CrossRefGoogle Scholar
  29. Millar NP, Reznick DN, Kinnison MT, Hendry AP (2006) Disentangling the selective factors that act on male color in wild guppies. Oikos 113:1–12. doi: 10.1111/j.0030-1299.2006.14038.x CrossRefGoogle Scholar
  30. Montgomerie R (2006) Analyzing colors. In: Hill GE, McGraw KJ (eds) Bird coloration, volume 1: mechanisms and measurements. Harvard University Press, Cambridge, pp 90–147Google Scholar
  31. Reebs SG (2002) Plasticity of diel and circadian activity in fishes. Rev Fish Biol Fish 12:349–371CrossRefGoogle Scholar
  32. Reynolds JD (1993) Should attractive individuals court more? Theory and a test. Am Nat 141:914–927. doi: 10.1086/285516 CrossRefPubMedGoogle Scholar
  33. Reynolds JD, Gross MD, Coombs MJ (1993) Environmental conditions and male morphology determines alternative mating behavior in Trinidadian guppies. Anim Behav 45:145–152. doi: 10.1006/anbe.1993.1013 CrossRefGoogle Scholar
  34. Reznick D, Endler JA (1982) The impact of predation on life history evolution in Trinidadian guppies (Poecilia reticulata). Evolution 36:160–177CrossRefGoogle Scholar
  35. Reznick D, Butler MJ, Rodd FH, Ross P (1996) Life-history evolution in guppies (Poecilia reticulata) 6. Differential mortality as a mechanism for natural selection. Evolution 50:1651–1660CrossRefGoogle Scholar
  36. Rice WR (1989) Analyzing tables of statistical tests. Evolution 43:223–225CrossRefGoogle Scholar
  37. Ringelberg J (1999) The photobehaviour of Daphnia spp. as a model to explain diel vertical migration in zooplankton. Biol Rev 74:397–423CrossRefGoogle Scholar
  38. Seghers BH (1973) Analysis of geographic variation in the antipredator adaptations of the guppy, Poecilia reticulata. PhD dissertation. University of British Columbia, British ColumbiaGoogle Scholar
  39. Smith EJ, Partridge JC, Parsons KN, White EM, Cuthill IC, Bennett ATD, Church SC (2002) Ultraviolet vision and mate choice in the guppy (Poecilia reticulata). Behav Ecol 13:11–19. doi: 10.1093/beheco/13.1.11 CrossRefGoogle Scholar
  40. van Oosterhout C, Joyce DA, Cummings SM, Blais J, Barson NJ, Ramnarine IW, Mohammed RS, Persad N, Cable J (2006) Balancing selection, random genetic drift, and genetic variation at the multiple compatibility complex in two wild populations of guppies (Poecilia reticulata). Evolution 60:2562–2574. doi: 10.1016/j.ijpara.2006.12.016 CrossRefPubMedGoogle Scholar
  41. Warren EW (1973) Effects of relative density upon some aspects of behavior of guppy, Poecilia reticulata (Peters). J Fish Biol 5:753–765CrossRefGoogle Scholar
  42. White EM (2003) Vision and visual behavior in teleost fish. PhD dissertation. University of Bristol, BristolGoogle Scholar
  43. White EM, Partridge JC, Church SC (2003) Ultraviolet dermal reflexion and mate choice in the guppy, Poecilia reticulata. Anim Behav 65:693–700. doi: 10.1006/anbe.2003.2117 CrossRefGoogle Scholar
  44. Zuk M, Kolluru GR (1998) Exploitation of sexual signals by predators and parasitoids. Q Rev Biol 73:415–438. doi: 10.1086/420412 CrossRefGoogle Scholar

Copyright information

© Springer-Verlag 2009

Authors and Affiliations

  • Gabrielle A. Archard
    • 1
    • 2
    Email author
  • Innes C. Cuthill
    • 1
  • Julian C. Partridge
    • 1
  1. 1.School of Biological SciencesUniversity of BristolBristolUK
  2. 2.School of Forest ResourcesThe Pennsylvania State UniversityState CollegeUSA

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