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For example, one of the biological mechanisms proposed on the basis of natural and sexual selection and explaining the existing cross-cultural differences in attractiveness preferences is the central tendency (Symons, 1979), i.e., preference for the average for particular traits.
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Thus, the change in apparent body size produced by the size-contrast illusion should be of sufficient magnitude to trigger an attractiveness preference between the target women.
Thus, our results provide a new perspective on the nature of sexual selection in general, and mating preference functions in particular, whose complexity will have to be embraced in future studies of the genetic underpinnings of attractiveness and preferences.
Importantly, we demonstrate that attractiveness and preferences of both males and females have a substantial genetic component, a result that agrees well with many other studies of the genetic basis of traits involved in sexual selection in a wide range of taxa (Merilä and Sheldon 1999; Rodriguez et al. 2013).
Virus infection causes biochemical, cellular, molecular, and physiological changes in host plants [ 13, 33, 34], some of which increase plant attractiveness and preference to vectors [ 35- 40].
The realized heritabilities in both attractiveness and preference are inconsistent in magnitude and direction among lines such that the mean heritability estimates are small, and not significantly different from zero (Table 2).
Jones said previous studies, testing thousands of women on the internet, showed a similar relationship between women's beliefs about their own attractiveness and their preferences for masculine characteristics in men's faces.
Mate attractiveness reflects female preferences only if females can sample adequate numbers of males of varying ornament size so that they can "get what they want" [50].
These results showed that leg length might not be a universal attractiveness marker and preferences for this body component could be related to a specific environment or culture.
An advantage over designs in which males and females are randomly paired and mated is that if mate choice is possible, linkage disequilibrium between male attractiveness and female preferences [ 1, 6] may be maintained [ 51, 52].
We spend the remainder of this paper considering why we failed to detect significant responses to three generations of selection on male attractiveness and female preferences, despite the widespread expectation that such a response should occur.
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