Evolutionary Ecology 1996, 10, 97-104
Sexual selection and the allometry of earwig forceps
L.W. SIMMONS and J.L. TOMKINS
Department of Environmental and Evolutionary Biology, University of Liverpool, POBox 147, Liverpool, L69 3BX,
UK
Summary
Positive intraspecific allometry, the tendency for large individuals to have relatively larger morphological
traits, is thought to be more likely for secondary sexual traits than naturally selected traits. This is because
secondary sexual traits are often used to signal individual quality and positive allometry should arise where
the costs and/or benefits of signalling are size dependent. Here we examine the allometric relationships
between forceps length, a sexually selected trait and elytra length, a naturally selected trait, in 42 species
of earwig. Both forceps and elytra showed positive allometry. However, the degree of allometry was greater
for forceps as predicted, ff ailometry arises due to sexual selection we would predict a greater degree of
allometry in species with more exaggerated secondary sexual traits. Across species, the degree of forcep
allometry did increase with forcep exaggeration. The relevance of positive allometry to reliable signalling
is discussed.
Keywords: Dermaptera; secondary sexual traits; positive allometry; display
Introduction
In his study of Megaloceros antlers, Gould (1973a) interpreted positive intraspecific allometry, the
tendency for larger individuals to possess relatively larger morphological traits, as an evolutionary
consequence of status signalhng by males, both to competitors and potential mates. Petrie (1988,
1992) proposed that in general positive allometry is more likely to occur in secondary sexual
traits than in other naturally selected traits. Because the outcome of competitive interactions is
usually determined by body size (Davies and Halliday, 1979; Sigurj6nsd6ttir and Parker, 1981;
Petrie, 1984; Simmons, 1986) it should pay large individuals to produce large secondary sexual
traits that signal competitive ability as this would reduce the number and/or intensity of agonistic
interactions in which they become involved. The same argument does not hold for small
individuals because they have little to gain from advertising low competitive ability and, further,
any costs associated with developing the trait are likely to outweigh the benefits of signalling
competitive ability. In general it has been argued that sexually selected traits may act as
handicaps in the sense that larger individuals may be better able to withstand the costs associated
with producing them (Zahavi, 1975; Andersson, 1986). Thus, the size of secondary sexual traits
may represent an honest signal of an individual's competitive ability (Parker, 1974; Alatalo et al.,
1988; Petrie, 1988). Green (1992) argued that secondary sexual traits that function in mate choice
should similarly show positive allometry, for example, if smaller individuals are less able to find
mates or are in lower phenotypic condition, they should invest relatively less in secondary sexual
displays required for mate attraction.
Positive allometric relationships have been found in the secondary sexual traits of a variety of
taxa (Huxley, 1931; Gould, 1973h; Brown and Bartalon, 1986; Alatalo et al., 1988; Petrie, 1988).
Nevertheless, positive allometry can be predicted for a variety of reasons and need not be specific
to secondary sexual traits. Although Green (1992) found a positive allometric relationship for tail
height, a sexually selected trait in male smooth newts, he also found positive allometry for male
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