In the highly sexual-dimorphic nocturnal moth, Acentria ephemerella Denis & Schiffermüller 1775, the aquatic and wingless female possesses a refracting superposition eye, whose gross structural organization agrees with that of the fully-winged male. The possession of an extensive corneal nipple array, a wide clear-zone in combination with a voluminous rhabdom and a reflecting tracheal sheath are proof that the eyes of both sexes are adapted to function in a dimly lit environment. However, the ommatidium of the male eye has statistically significantly longer dioptric structures (i.e., crystalline cones) and light-perceiving elements (i.e., rhabdoms), as well as a much wider clear-zone than the female. Photomechanical changes upon light/dark adaptation in both male and female eyes result in screening pigment translocations that reduce or dilate ommatidial apertures, but because of the larger number of smaller facets of the male eye in combination with the structural differences of dioptric apparatus and retina (see above) the male eye would enjoy superior absolute visual sensitivity under dim conditions and a greater resolving power and ability to detect movement during the day. The arrangement of the microvilli in the rhabdom of both genders suggests that their eyes are polarization-sensitive, an ability they would share with many aquatic insects that have to recognize water surfaces. Although sexual recognition in A. ephemerella is thought to chiefly rely on pheromones, vision must still be important for both sexes, even if the females are wingless and never leave their watery habitat. Females swim actively under water and like their male counterparts, which fly above the surface of the water, they would have to see and avoid obstacles as well as potential predators. This, together with a small incidence of winged females, we believe, could be the reason why the eyes of female A. ephemerella are less regressed than those of other sexually dimorphic moths, like for instance Orgyia antiqua. Another, but difficult to test, possibility is that male and female A. ephemerella have diverged in their behaviour and habitat preferences less long ago than other sexually dimorphic moths.
Structure and photomechanical changes upon light/dark adaptation in the superposition compound eyes of the highly sexually dimorphic Orygia antiqua were studied by light and electron microscopy. The eyes of the fully winged male differ from those of the wingless, sedentary female in several respects: they are significantly larger, display a more regular ommatidial array, have a wider clearzone and possess a much more substantial tracheal tapetum. However, the eyes of the female exhibit more pronounced photomechanical changes upon light/dark adaptation than those of the male. We believe that for females, on account of their limited mobility, it is necessary that their eyes can cope with widely fluctuating brightnesses, but that visual sensitivity and resolving power are less important to them than to the actively flying males. Although the latter may be attracted to the females by pheromones, males in their diurnal searches will have to visually avoid obstacles and predators. Moreover, because of their ability to fly, males can seek shelters or shaded areas and unlike the sedentary females avoid prolonged exposures to potentially hazardous light levels. This could explain why the eyes of the females exhibit more pronounced photomechanical responses to changes in ambient light levels.