Movements of fireflies visible on the surface of soil were measured under controlled laboratory conditions consisting of high and low ambient illumination. High illumination approximating the intensity of light prior to sunset constituted our light condition. Low illumination was consistent with ambient light levels after civil sunset, which we referred to as our dark condition. Surface movements were significantly more frequent during dark conditions compared to light conditions. Stemmata are the larval form of the insect eye and were the only identified visual organs present in Photuris larvae. We investigated whether stemmata provided larvae with the sensory information facilitating the light dependency of surface movements. We disrupted transmission of visual information from the larval eyes to the brain by severing the optic nerves. The amount of surface movement was compared between larvae with intact and severed optic nerves, under light and dark conditions. Light dependency of surface movements was preserved in larvae with cut optic nerves. The presence of the light dependency after cutting the optic nerves indicated that an alternative, extrastemmatal sensory pathway must be providing light intensity information to the animal. Light dependency was abolished upon removal of the head. Thus, these results suggested that the extraocular system providing light intensity information for regulating the frequency of surface movement was located in the head. The precise location of the suggested extraocular receptor and the nature of the associated sensory system remains unknown.

Fireflies (Coleoptera: Lampyridae) have distinct visual systems at different stages of development. Larvae have stemmata and adults have compound eyes. Adults use compound eyes to mediate photic communication during courtship. Larvae do not manifest this behavior, yet they are bioluminescent. We investigated the structure of stemmata in Photuris firefly larvae to identify anatomical substrates (i.e., rhabdomeres) conferring visual function. Stemmata were located bilaterally on the antero-lateral surfaces of the head. Beneath the ~ 130 µm diameter lens, we identified a pigmented eye-cup. At its widest point, the eye-cup was ~ 150 µm in diameter. The optic nerve exited the eye-cup opposite the lens. Two distinct regions, asymmetric in size and devoid of pigmentation, were characterized in stemmata cross-sections. We refer to these regions as lobes. Each lobe contained a rhabdom of a radial network of rhabdomeres. Pairs of rhabdomeres formed interdigitating microvilli contributed from neighboring photoreceptor cell bodies. The optic nerve contained 88 axons separable into two populations based on size. The number of axons in the optic nerve together with distinct rhabdoms suggests these structures were formed from ‘fusion stemmata.’ This structural specialization provides an anatomical substrate for future studies of visually mediated behaviors in Photuris larvae.