The complete mitochondrial genome of a pyraloid species, Palpita hypohomalia, was sequenced and analyzed. This mitochondrial genome is circular, 15,280 bp long, and includes 37 typical metazoan mitochondrial genes (13 protein-coding genes, two ribosomal RNA genes, 22 transfer RNA genes) and an A + T-rich region. Nucleotide composition is highly biased toward A + T nucleotides (81.6%). All 13 protein-coding genes (PCGs) initiate with the canonical start codon ATN, except for cox1 which is CGA. The typical stop codon TAA occurs in most PCGs, while nad2 and cox2 show TAG and an incomplete termination codon T, respectively. All tRNAs have a typical clover-leaf structure, except for trnS1 (AGN) which lacks the dihydrouridine (DHU) arm. Comparative mitochondrial genome analysis showed that the motif "ATGATAA" between atp8 and atp6, and the motif "ATACTAA" between trnS2 and nad1 were commonly present in lepidopteran mitogenomes. Furthermore, the "ATAG" and subsequent poly-T structure, and the A-rich 3' end were conserved in the A + T-rich regions of lepidopteran mitogenomes. Phylogenetic analyses based on our dataset of 37 mitochondrial genes yielded identical topology for the Pyraloidea, and is generally identical with that recovered by a previous study based on multiple nuclear genes. In a previous study of the Crambidae, the Evergestinae was synonymized with Glaphyriinae; the present study is the first to clarify their close relationship with mitogenome data.
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.