Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Reinforcement of pre-zygotic isolation and karyotype evolution in Agrodiaetus butterflies

Abstract

The reinforcement model of evolution argues that natural selection enhances pre-zygotic isolation between divergent populations or species by selecting against unfit hybrids1,2 or costly interspecific matings3. Reinforcement is distinguished from other models that consider the formation of reproductive isolation to be a by-product of divergent evolution4,5. Although theory has shown that reinforcement is a possible mechanism that can lead to speciation6,7,8, empirical evidence has been sufficiently scarce to raise doubts about the importance of reinforcement in nature6,9,10. Agrodiaetus butterflies (Lepidoptera: Lycaenidae) exhibit unusual variability in chromosome number. Whereas their genitalia and other morphological characteristics are largely uniform, different species vary considerably in male wing colour, and provide a model system to study the role of reinforcement in speciation. Using comparative phylogenetic methods, we show that the sympatric distribution of 15 relatively young sister taxa of Agrodiaetus strongly correlates with differences in male wing colour, and that this pattern is most likely the result of reinforcement. We find little evidence supporting sympatric speciation: rather, in Agrodiaetus, karyotypic changes accumulate gradually in allopatry, prompting reinforcement when karyotypically divergent races come into contact.

Your institute does not have access to this article

Relevant articles

Open Access articles citing this article.

Access options

Buy article

Get time limited or full article access on ReadCube.

$32.00

All prices are NET prices.

Figure 1: Changes in male wing coloration along the phylogeny of Agrodiaetus.
Figure 2: Changes in male wing coloration between Agrodiaetus sister clades as a function of their genetic distance.
Figure 3: Age–range correlation plot.
Figure 4: Agrodiaetus karyotypic diversity strongly correlates with nucleotide divergence ( R 2 = 0.820; P < 0.002).

References

  1. Dobzhansky, T. Speciation as a stage in evolutionary divergence. Am. Nat. 74, 312–321 (1940)

    Article  Google Scholar 

  2. Noor, M. A. F. Speciation driven by natural selection in Drosophila. Nature 375, 674–675 (1995)

    ADS  CAS  Article  Google Scholar 

  3. Coyne, J. A. & Orr, A. H. Speciation (Sinauer Associates, Sunderland, Massachusetts, 2004)

    Google Scholar 

  4. Mayr, E. Population, Species, and Evolution; an Abridgment of Animal Species and Evolution (Harvard Univ. Press, Cambridge, Massachusetts, 1970)

    Google Scholar 

  5. Turelli, M., Barton, N. & Coyne, J. Theory and speciation. Trends Ecol. Evol. 16, 330–343 (2001)

    CAS  Article  Google Scholar 

  6. Noor, M. A. F. Reinforcement and other consequences of sympatry. Heredity 83, 503–508 (1999)

    Article  Google Scholar 

  7. Kirkpatrick, M. & Ravigne, V. Speciation by natural and sexual selection: models and experiments. Am. Nat. 159, S22–S35 (2002)

    Article  Google Scholar 

  8. Servedio, M. R. & Noor, M. A. F. The role of reinforcement in speciation: theory and data. Annu. Rev. Ecol. Evol. Syst. 34, 339–364 (2003)

    Article  Google Scholar 

  9. Butlin, R. K. Species, speciation, and reinforcement. Am. Nat. 130, 461–464 (1987)

    Article  Google Scholar 

  10. Marshall, J. L., Arnold, M. L. & Howard, D. J. Reinforcement: the road not taken. Trends Ecol. Evol. 17, 558–563 (2002)

    Article  Google Scholar 

  11. Coyne, J. A. & Orr, H. A. Patterns of speciation in Drosophila. Evolution 43, 362–381 (1989)

    Article  Google Scholar 

  12. Coyne, J. A. & Orr, A. H. “Patterns of speciation in Drosophila” revisited. Evolution 51, 295–303 (1997)

    Article  Google Scholar 

  13. Sætre, G.-P. et al. A sexually selected character displacement in flycatchers reinforces premating isolation. Nature 387, 589–592 (1997)

    ADS  Article  Google Scholar 

  14. Jiggins, C. D., Naisbit, R. E., Coe, R. L. & Mallet, J. Reproductive isolation caused by colour pattern mimicry. Nature 411, 302–305 (2001)

    ADS  CAS  Article  Google Scholar 

  15. Nosil, P., Crespi, B. J. & Sandoval, C. P. Reproductive isolation driven by combined effects of ecological adaptation and reinforcement. Proc. R. Soc. Lond. B 270, 1911–1918 (2003)

    CAS  Article  Google Scholar 

  16. Templeton, A. R. Mechanisms of speciation – a population genetic approach. Annu. Rev. Ecol. Syst. 12, 23–48 (1981)

    Article  Google Scholar 

  17. Butlin, R. K. Reinforcement: an idea evolving. Trends Ecol. Evol. 10, 432–434 (1995)

    CAS  Article  Google Scholar 

  18. Day, T. Sexual selection and the evolution of costly female preference: spatial effects. Evolution 54, 715–730 (2000)

    CAS  Article  Google Scholar 

  19. Kandul, N. P. et al. Phylogeny of Agrodiaetus Hübner 1822 (Lepidoptera: Lycaenidae) inferred from mtDNA sequences of COI and COII, and nuclear sequences of EF1-a: karyotype diversification and species radiation. Syst. Biol. 53, 278–298 (2004)

    Article  Google Scholar 

  20. Lesse, de H. Spéciation et variation chromosomique chez les Lépidoptères Rhopalocères. Ann. Sci. Nat. Zool. Biol. Anim. 2, 1–223 (1960)

    Google Scholar 

  21. Lukhtanov, V. A. & Danchenko, A. D. Principles of the highly ordered arrangement of metaphase I bivalents in spermatocytes of Agrodiaetus (Insecta, Lepidoptera). Chromosome Res. 10, 5–20 (2002)

    CAS  Article  Google Scholar 

  22. Hagen, W. T. Freilandhybriden bei Blaeulingen aus Ostanatolien und Iran (Lepidoptera: Lycaenidae). Nachr. entomol. Ver. Apollo 23, 199–203 (2003)

    Google Scholar 

  23. Schurian, K. G. & Hofmann, P. Ein neuer Lycaeniden-Hybrid: Agrodiaetus ripartii Freyer x Agrodiaetus menalcas Freyer (Lepidoptera: Lycaenidae). Nachr. entomol. Ver. Apollo 1, 21–23 (1980)

    Google Scholar 

  24. Lorkovíc, Z. in Butterflies of Europe (ed. Kudrna, O.) 332–396 (Aula, Wiesbaden, 1990)

    Google Scholar 

  25. Fordyce, J. A., Nice, C. C., Forister, M. L. & Shapiro, A. M. The significance of wing pattern diversity in the Lycaenidae: mate discrimination by two recently diverged species. J. Evol. Biol. 14, 871–879 (2002)

    Article  Google Scholar 

  26. Vane-Wright, R. I. & Boppre, M. Visual and chemical signalling in butterflies: functional and phylogenetic perspective. Phil. Trans. R. Soc. Lond. B 340, 197–205 (1993)

    ADS  Article  Google Scholar 

  27. Bernard, G. D. & Remington, C. Color vision in Lycaena butterflies: spectral tuning of receptor arrays in relation to behavioural ecology. Proc. Natl Acad. Sci. USA 88, 2783–2787 (1991)

    ADS  CAS  Article  Google Scholar 

  28. Drummond, B. A. in Sperm Competition and the Evolution of Animal Mating Systems (ed. Smith, R. L.) 291–370 (Academic, San Diego, California, 1984)

    Book  Google Scholar 

  29. Felsenstein, J. Phylogenies and the comparative method. Am. Nat. 125, 1–15 (1985)

    Article  Google Scholar 

  30. Barraclough, T. G. & Vogler, A. P. Detecting the geographic pattern of speciation from species-level phylogeny. Am. Nat. 155, 419–434 (2000)

    PubMed  Google Scholar 

Download references

Acknowledgements

We thank A. J. Berry, J. A. Coyne, S. V. Edwards, J. R. Morris and R. Vila for their advice during the preparation of this manuscript. C. Bilgin, J. Coleman, F. Fernández-Rubio, G. Grigorjev, J. Jubany, C. Ibánez, R. Martínez, M. L. Munguira, C. Sekercioglu, C. Stefanescu, M. A. Travassos, R. Vila and V. Zurilina helped with collecting specimens, and J. Coleman and R. Vila assisted with sequencing in the laboratory. W. H. Piel and A. Monteiro helped us to measure wing ultraviolet reflectance. This research was supported by three collecting grants from the Putnam Expeditionary Fund of the Museum of Comparative Zoology, Harvard University; a National Science Foundation Doctoral Dissertation Improvement Grant to N.P.K.; National Science Foundation and Baker Foundation grants to N.E.P.; Milton Fund grants to D.H. and J.B.P.; a Burroughs Wellcome Fund grant to J.B.P.; and grants from the Russian Foundation for Basic Research, and the Russian Federal Programs “Universities of Russia” and “Leading Scientific Schools” to V.A.L.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Naomi E. Pierce.

Ethics declarations

Competing interests

The sequences have been deposited in GenBank; see Supplementary Appendix 1 for details. Reprints and permissions information is available at npg.nature.com/reprintsandpermissions. The authors declare no competing financial interests.

Supplementary information

Supplementary Notes

This file contains Supplementary Methods, Supplementary Figures S1-S7, Supplementary Tables S1-S5, Supplementary Discussion and additional references. (PDF 4253 kb)

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Lukhtanov, V., Kandul, N., Plotkin, J. et al. Reinforcement of pre-zygotic isolation and karyotype evolution in Agrodiaetus butterflies. Nature 436, 385–389 (2005). https://doi.org/10.1038/nature03704

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nature03704

Further reading

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing