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Unfortunately, honeybee mating choices are more difficult to control than those of pea plants, and honeybee genetics are different to pea plants, as well.
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Indeed, some differences between preferences for cues of BMI and actual mate choices would be expected, given that mate choices are likely to be constrained in ways that mate preferences are not.
However, the cellular/molecular basis of visual-based mate choice remain largely obscure, whereas those of the olfactory/auditory-based mate choices are understood in greater detail for model organisms such as mice, fruit flies, or nematodes [ 6- 8].
Relationships among mean male quality, follicular volume, mass, and mate choice are listed in Table 1.
The genetic benefits of mate choice are limited by the degree to which male and female fitness are genetically correlated.
Empirical studies suggest that direct benefits of female mate choice are more important than indirect benefits in some taxa [46] [48].
More direct measures of the effect of dewlap color on male-male competition and female mate choice are needed to assess the sexual selection hypothesis.
Detailed analysis of the benefits of mate choice are scarce in parasitoids though.
Direct and indirect selection on mate choice are expected to cause substantial evolutionary change [ 4, 9- 11, 26].
We do not yet know whether olfactory signals involved in mate choice are expressed by both sexes.
Models of sexual selection by mate choice are classified by the mechanism of evolution of mating preferences (Kirkpatrick and Ryan 1991).
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