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Comparative Study
.2007 Jul 22;274(1619):1789-94.
doi: 10.1098/rspb.2007.0451.

Temporal order and the evolution of complex acoustic signals

Affiliations
Comparative Study

Temporal order and the evolution of complex acoustic signals

H Carl Gerhardt et al. Proc Biol Sci..

Abstract

The evolution of complex signals may be favoured by hidden preferences or pre-existing sensory biases. Females of two species of grey treefrogs (Hyla chrysoscelis and Hyla versicolor) were tested with combinations of a conspecific advertisement call and acoustic appendages. Appendages consisted of aggressive calls and segments of advertisement calls from conspecific males and males of three other species and bursts of filtered noise. When a wide variety of these acoustic appendages followed the advertisement call, the resulting compound signal was often more attractive than the same advertisement call alone. When the same appendages led advertisement calls, however, the compound signal was never more attractive and sometimes less attractive. The order effect was especially strong in tests of H. versicolor in which advertisement-call duration was decreased. These results cannot be explained by a general pre-existing bias for extra stimulation per se. Rather, order and other effects may constrain the evolution and subsequent modification of complex and extravagant signals, examples of which have been reported for a wide range of taxa.

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Figures

Figure 1
Figure 1
Oscillograms and sonograms of representative acoustic stimuli: (a)H. chrysoscelis control stimulus showing timing relationship with the alternative (same advertisement call; oscillogram only); (b) normal-duration advertisement call ofH. versicolor and following aggressive call ofH. arenicolor; (c) aggressive call ofH. avivoca leading short-duration advertisement call ofH. versicolor; and (d) normal-duration call ofH. chrysoscelis and following aggressive call ofH. versicolor.
Figure 2
Figure 2
Choices of female grey treefrogs in tests of compound calls versus normal-duration advertisement calls alone. (a) Proportions of females (n=32 females per test) ofH. versicolor andH. chrysoscelis choosing compound calls in tests in which appendages followed advertisement calls. Filled symbols,H. versicolor females; open symbols,H. chrysoscelis females; circles, advertisement-call appendages; squares, aggressive-call appendages; triangles, noise-burst appendage; stars, control compound calls (see text). (b) Results of tests in which the appendage led the advertisement call. The 95% exact confidence limits were computed using theF-distribution method employed in SAS v. 11.1, and hence are not always symmetrical around the observed proportion. We interpret them as Bayesian credible intervals (uniform prior distribution).
Figure 3
Figure 3
Proportions of females ofH. versicolor (n=32 females per test) choosing compound calls with appendages added to an advertisement call of shorter-than-average duration. Filled symbols, appendage in following position; open symbols, appendage in leading position; circle, advertisement-call appendage; square, aggressive-call appendage; triangle, noise-burst appendage; star, control test with conspecific advertisement-call segment.
Figure 4
Figure 4
Proportions of females ofH. versicolor andH. chrysoscelis choosing compound calls in two-speaker choice tests in a randomized block design using aggressive-call appendages. Filled symbols, appendages in the following position; open symbols, appendages in the leading position. Error bars are 95% credible (confidence) intervals. (a) Proportions of females ofH. versicolor (n=50) choosing compound calls with appendages added to a normal-duration advertisement call. (b) Proportions of females ofH. versicolor (n=20) choosing compound calls with appendages added to a shorter-than-average advertisement call. (c) Proportions of females ofH. chrysoscelis (n=30) choosing compound calls with appendages added to a normal-duration advertisement call.
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References

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