ten Cate, C. and Verzijden, M.
(2006). Sexual imprinting can induce sexual preferences for
exaggerated parental traits. Current Biology, 16, 1128-1132.
This
study assessed whether sexual imprinting in zebra finch could give rise to peak
shift in male mate preference. Previous studies have shown that zebra finch
learn sexually dimorphic signals through imprinting their parentŐs traits.
Males tend to choose mates based on beak color, and prefer beak colors that
match their mother while avoiding females that match their father. The
researchers wished to test whether this learning process could be affected by
peak shift. Peak shift is a well-documented, inherent part of discriminative
learning. When animals learn to discriminate between two similar stimuli, they
tend to over-generalize the desired stimuli to distinguish it further from the
undesired stimuli. In this study, the researchers expected the male zebra
finches to over-generalize the color of their motherŐs beak and prefer females
with even more exaggerated ŇmotherÓ coloration.
To
test this hypothesis, the researchers used nail polish to experimentally manipulate
the beak color of white parents raising broods of males. In one group the
motherŐs beak was painted orange and the fatherŐs beak red and in another group
the colors were reversed. After the males had reached sexual maturity they were
presented with eight females whose beak color had also been manipulated with
polish. Some of the females were the same color as the father and mother and
other females had orange and red colors that were more exaggerated than the
parentsŐ colors. The malesŐ preferences were measured by how many mating song
the males sang at the females they saw. As expected, males preferred females
that had the same color as the mother, and they further preferred the more
exaggerated coloration (purer orange or red). The males also tended to sing
less to females that matched or exaggerated the fathersŐ color. These results
suggest that males base their mate choice on learned sexually dimorphic signals
and that this learning results in peak shift of color preference.
This
study gives an alternative explanation for the origins of sexually dimorphic
and exaggerated sexual signals. In class we discussed the idea that sexual
signals may be arise because of inherent receiver biases or feature detectors that
are naturally tuned to particular colors, movements, sounds, etc. We also
discussed the possibility that some signals may be honest signs of an animalŐs
condition, and can thus be used by others to assess the viability of mates. We
did not discuss how the learning process itself may shape the evolution of
signals. This study has shown that peak shift does occur for the zebra finch
(and presumably in other animals that learn from parent models how to
distinguish between the sexes). Peak shift can explain how sexual signals can
evolve into more exaggerated traits because each successive generation prefers
a more exaggerated form of the parent model. This explanation is not
appropriate for all animals and does not exclude the possibility of the other
theories also contributing to the evolution of sexual signals.