Quantitative genetics research in Zebra Finches: where we are and where to go
Barbara Tschirren A and Erik Postma B CA Department of Animal Ecology, Sölvegatan 37, Lund University, S-223-62 Lund, Sweden.
B Institute of Evolutionary Biology and Environmental Studies, University of Zürich, Winterthurerstrasse 190, CH-8057 Zürich, Switzerland.
C Corresponding author. Email: erik.postma@ieu.uzh.ch
Emu 110(3) 268-278 https://doi.org/10.1071/MU09092
Submitted: 16 September 2009 Accepted: 12 January 2010 Published: 18 August 2010
Abstract
The ease with which Zebra Finches can be kept and bred in captivity makes them a suitable model for avian quantitative genetic studies. After a brief introduction to some quantitative genetic concepts, we here provide an up-to-date overview of quantitative genetic studies in Zebra Finches. We discuss what these studies can teach us about the evolutionary and behavioural ecology of Zebra Finches and song birds in general, and make suggestions for future research. Throughout this article we plead for a greater appreciation of the advantages offered by working on captive birds, but also discuss their limitations. Although quantitative genetic analyses in natural populations are becoming increasingly powerful, these studies lack the control possible in captivity. However, obtaining meaningful estimates of the type and strength of selection acting on phenotypic variation is more difficult in captivity. Hence, quantitative genetic studies in the wild and captivity each have their strengths and weaknesses and should be considered complementary rather than opposing. However, whereas quantitative genetic studies in the wild have boomed, the unique advantages offered by captive Zebra Finches have remained underexploited. Here we make a first attempt at changing this by highlighting what we believe may be fruitful lines for future research.
Acknowledgements
We thank the editors, as well as Wolfgang Forstmeier and an anonymous reviewer for comments on this manuscript. The Swiss National Science Foundation (SNF) financially supported B. Tschirren (Fellowship no. PA00A3–121466) and E. Postma (grant 31003A-116794) during the writing of this review.
Airey, D. C. , and DeVoogd, T. J. (2000). Greater song complexity is associated with augmented song system anatomy in zebra finches. Neuroreport 11, 2339–2344.
| Crossref | GoogleScholarGoogle Scholar | PubMed |
Festing, M. F. W. (1999). Warning: the use of heterogeneous mice may seriously damage your research. Neurobiology of Aging 20, 237–244.
| Crossref | GoogleScholarGoogle Scholar | PubMed |
Gil, D. , Graves, J. , Hazon, N. , and Wells, A. (1999). Male attractiveness and differential testosterone investment in zebra finch eggs. Science 286, 126–128.
| Crossref | GoogleScholarGoogle Scholar | PubMed |
Munsell, A. H. (1912). A pigment color system and notation. The American Journal of Psychology 23, 236–244.
| Crossref | GoogleScholarGoogle Scholar |
Price, D. K. (1996). Sexual selection, selection load and quantitative genetics of zebra finch bill colour. Proceedings of the Royal Society of London. Series B. Biological Sciences 263, 217–221.
| Crossref | GoogleScholarGoogle Scholar |
Rønning, B. , Moe, B. , and Bech, C. (2005). Long-term repeatability makes basal metabolic rate a likely heritable trait in the zebra finch Taeniopygia guttata. Journal of Experimental Biology 208, 4663–4669.
| Crossref | GoogleScholarGoogle Scholar | PubMed |
Silverin, B. (1998). Stress responses in birds. Poultry and Avian Biology Reviews 9, 153–168.