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editior about Audience drives male songbird response to partner s voice

Vignal, Clémentine; Mathevon, Nicolas; Mottin, Stéphane

Abstract

According to the social intelligence hypothesis, social context represents an important force driving the selection of animal cognitive abilities such as the capacity to estimate the nature of the social relationships between other individuals (1, 2, 3, 4). Despite this importance, the influence of this force has been assessed only in primates and never in other animals showing social interactions (5, 6, 7). In this way, avian communication generally takes place in a network of signallers and receivers, which represents an audience altering individual signalling behaviours (8, 9). Indeed, vocal amplitude (10) and repertoire (11) are known to be socially regulated and the attitude towards the opposite sex may change depending on the audience (8, 12, 13). This audience effect (8, 14, 15, 16) provides support for the reality of social awareness in some bird species. However no evidence has yet been found to suggest that birds are able to estimate the characteristics of the social relationships between group-mates. Here we show that the male of a gregarious songbird species—the zebra finch (Taeniopygia guttata)—pays attention to the mating status of conspecific pairs, and uses this information to control its behaviour towards its female partner.

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activation during singing in zebra finches found that the areas of the brain responsible for song production and for perception are differentially activated according to the social context in which the bird is placed. Both in vivo electrophysiological recordings and assessment of early gene activity indicated that different brain areas are activated depending on whether the males are singing alone or with a female.As all previous studies of mate recognition by male zebra finches were conducted when the bird was alone, could it be that differences in social context modify recognition behaviour in an analogous way to the modification of brainactivation patterns? To address this question directly, Vignal et al.3played back either the mate’s call or a familiar female’s call to male zebra finches in three different ‘social’ conditions: with two unmated males,with a mated pair or with an unmated pair. The results were striking. When male zebra finches were with either unmated males or an unmated pair, they showed no greater response to their mate’s call than to the call of a familiar female. That is, males called back at about equal rates in response to both their mate’s calls and those of the familiar female. But when males were exposed to calls in the presence of a mated pair, the differences were marked: males called back almost twice as often in response to their mate’s calls as to the familiar female’s calls. These results are intriguing on several levels, and will undoubtedly provide fodder for future research. First, Vignal et al. show that even a seemingly simple call can contain enough information to be identified individually. Equally interesting is how this comes about in female zebra finches, which until now had been thought to be unable to learn vocalizations like males of the species. Further, how do social context and the male’s recognition ability interact? Do males recognize their mates in all social situations but express this ability only in certain ones? Or does the social situation itself activate the brain areas required for recognition, facilitating the recognition process? Perhaps the most important implication of this study is that we primates are not alone in our ability to judge social context.It seems that birds are far more aware of such niceties than we have previously given them credit for. ■ Christopher B. Sturdy is in the Department of Psychology, Centre for Neuroscience, University of Alberta, Edmonton AB T6G 2E9, Canada. e-mail: [email protected] 1. Zann, R. The Zebra Finch: A Synthesis of Field and Laboratory Studies (Oxford Univ. Press, 1996). 2. Miller,D.B.Anim. Behav. 27, 376–380 (1979). 3. Vignal, C., Mathevon, N. & Mottin, S. Nature 430, 448–451 (2004). 4. Hessler, N. A. & Doupe, A. J. Nature Neurosci. 2, 209–211 (1999). 5. Jarvis, E. D., Scharff, C. & Grossman, M. R. Neuron 21, 775–788 (1998). news and views 414 NATURE | VOL 430 | 22 JULY 2004 | www.nature.com/nature this phase, both static and dynamic, must be explored, creating a new area of research in the field of liquid-crystal science and technology. ■ Geoffrey R. Luckhurst is in the School of Chemistry, University of Southampton, Highfield, Southampton SO17 1BJ, UK. e-mail: [email protected] 1. Madsen, L. A., Dingemans, T. J., Nakata, M. & Samulski, E. T. Phys. Rev.Lett. 92, 145505 (2004). 2. Acharya, B. R., Primak, A. & Kumar, S. Phys. Rev.Lett. 92, 145506 (2004). 3. Freiser, M. J. Phys. Rev.Lett. 24, 1041–1043 (1970). Animal behaviour A social call Christopher B. Sturdy An indicator of animal intelligence is thought to be the ability to judge relationships between members of the same species. This talent, previously seen only in primates, seems to be evident in a bird. Zebra finches are small, colonial songbirds native to Australia, and they have been favourite subjects of biologists for years1.Most studies have focused on the birds’ vocal-communication behaviour, and many insights have emerged from such research. For example, female zebra finches can recognize their mate, with whom they form lasting pair bonds, by his ‘distance call’, one of the most frequent vocalizations of these finches2.But the early studies found no reciprocal recognition — male zebra finches did not recognize their mate through female distance calls. The reason for this was unclear, although it was speculated that, as the females’ calls have a simpler acoustic structure than those of the males, the calls contained fewer individually recognizable features. One overlooked factor was the context in which these recognition tests were conducted. The birds, normally members of large flocks in the wild or large groups in captivity, had been tested while alone. On page 448 of this issue,Vignal et al.3suggest not only that female zebra finch distance calls are individualized, but that social isolation in the previous tests was the primary cause of the male’s apparent recognition failure. They go a step further, showing that, remarkably, the males respond to their mate’s calls according to the social situation. This latter finding suggests for the first time that a nonprimate may be able to assess the social relationships between other animals of its own E. JANES/NHPA species, an ability thought to be a mark of intelligence. To determine whether the females’ distance calls had the potential for individual recognition, Vignal et al.3analysed the acoustic structure of calls from seven female zebra finches. Several features were measured to characterize each female’s call. By quantifying the variability of each acoustic feature in each bird and comparing these with the variability found for the group, Vignal et al. concluded that certain features were sufficiently individualized to allow recognition. Further, when these features were analysed in more detail, the authors found that they could identify individual females with 100% accuracy. Clearly, males should be able to identify their mate’s calls. Why, then, was this not seen before? And what might facilitate this recognition process in male zebra finches? The answer seems to lie in the birds’brains. Two neurobiological studies4,5 of brain In mixed company: Vignal et al.3find that male zebra finches (with orange cheek patches and chestnut flanks) respond to their mate’s call in a manner that depends on the social context. 4. Praefcke, K. et al.Mol. Cryst. Liq. Cryst. 198, 393–405 (1991). 5. Malthête, J., Nguyen, H. T. & Levelut, A. M. J. Chem. Soc. Chem. Commun. 1548–1549 (1986); Corrigendum 40 (1987). 6. Chandrasekhar, S., Ratna, B. R., Sadashiva, B. K. & Raja, N. V. Mol. Cryst. Liq. Cryst. 165, 123–130 (1988). 7. Praefcke, K. et al. Liq. Cryst. 7, 589–594 (1990). 8. Galerne, Y. Mol. Cryst. Liq. Cryst. 323, 211–229 (1998). 9. Luckhurst, G. R. Thin Solid Films 393, 40–52 (2001). 10.Yu, L.J.& Saupe,A.Phys. Rev. Lett.45, 1000–1003 (1980). 11.Severing, K. & Saalwächter, K. Phys. Rev. Lett.92, 125501 (2004). 12.Teixeira, P. I. C., Masters, A. J. & Mulder, B. M. Mol. Cryst. Liq. Cryst. 323, 167–189 (1998). 13.Dingemans, T. J. & Samulski, E. T. Liq. Cryst. 27, 131–136 (2000). 22.7 n&v 409 MH 16/7/04 5:23 pm Page 414 © 2004Nature Publishing Group