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The sex and sex x morph interaction were not significant (both P>0.3).
The treatment by wing morph interaction term assessed whether the relationship between wing morph and the traits of interest remained the same in both the diet environments.
We then used the resulting model to assess if the relationship between male mating investment and the other traits of interest differed significantly between the different diet treatments and wing morph types by assessing separately if the treatment or wing morph interaction terms improved the fit of the regression model.
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For all traits measured there were no significant differences between the micropterous and macropterous individuals and there were no significant treatment by wing morph interactions.
For all traits measured, the treatment by wing morph interactions were not significant, indicating that the effect of wing morph on the number of copulations and male attractiveness was consistent across the experimental populations of both diet quality treatments.
The effect of diversity on survival in high density did not differ among relatedness treatments (effect of the Relatedness * Morphs (linear) interaction: χ2 = 2.82, d.f.
The model thus included sex, morph and their interaction (Table 1).
However, there was also a significant morph by sex interaction (Table 2), such that melanic females were in better condition than the other three groups (Fig. 2D).
Moreover, the significant morph × sex interaction indicates a divergence of sexual size dimorphism between morphs.
A significant morph × population interaction was found in all three species as well, which indicates that the effects of morph type on SSD depend on the population source.
However, remarkably few empirical studies have evaluated how social interactions, morph frequencies and fitness parameters relate to one another under natural conditions.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com