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Additional resources for Evolutionary Developmental Biology (Evo-Devo) and Behaviour (Philosophical Transactions of the Royal Society series B) issue 1574
15, 430– 438. (doi:10. , Tabin, C. & Carroll, S. 2009 Deep homology and the origins of evolutionary novelty. Nature 457, 818 –823. , King, V. , Bentley, G. E. & Ball, G. F. 2001 Photoperiodic control of seasonality in birds. J. Biol. Rhythms 16, 365–380. 1177/074873001129002079) Nicholls, T. , Goldsmith, A. R. & Dawson, A. 1988 Photorefractoriness in birds and comparison with mammals. Physiol. Rev. 68, 133–176. Wiltschko, W. & Wiltschko, R. 1972 Magnetic compass of European robins. Science 176, 62– 64.
Neuroreport 9, 3047–3052. , Bolhuis, J. J. & Kimura, T. 2003 Neuronal activation in female budgerigars is localized and related to male song complexity. Eur. J. Neurosci. 17, 149–154. x) 17 Gentner, T. , Hulse, S. , Duffy, D. & Ball, G. F. 2001 Response biases in auditory forebrain regions of female songbirds following exposure to sexually relevant variation in male song. J. Neurobiol. 46, 48– 58. CO;2-3) 18 Maney, D. , MacDougall-Shackleton, E. , MacDougall-Shackleton, S. , Ball, G. F. & Hahn, T.
The overall output of the network may be maintained through homeostatic mechanisms allowing different combinations of ion channels and synapses to achieve a similar set point of activity [91–93]. Thus, if species-specific motor behaviours were caused by differences in the biophysical properties of the neurons and synapses, it would probably involve a suite of biophysical differences rather than one or two small differences. This could be good news for studying the evolution of neural circuits because it means that species differences that underlie behaviour are likely to be substantial, rather than subtle.