As a part of a comparative study of plant and animal photoreceptor structures we have been investigating the spectral response and structure of the compound eye of the insect Drosopldla melanogaster (14). The compound eye of Drosophila is composed of approximately 700 ommatidia with each ommatidinm consisting of seven retinula cells radially arranged forming a cylinder. Each retinula cell has a differentiated structure, the rhabdomere. Since the earliest investigations (5, 6) the rhabdomeres have been considered the "light trapping" area where the visual process is initiated. In three eye color mutants, scarlet, wild-type red, and white, we have found that the action or effectiveness spectrum is indicative of a pigment absorbing at 508 m~, similar in absorption spectra to the visual complexes found in the vertebrate photoreceptors, but not similar in absorption spectra to any of the eye pigment extracts isolated from these mutants (14). We have assumed that the extractable pigments are from the sheath of pigment cells surrounding each ommatidium and that the action spectrum is indicative of a "visual" pigment, not as yet isolated or identified, residing within the rhabdomeres. Recent electron micrographs of the ommatidia in the house fly (3) as well as our own electron microscopic studies indicate a general "fine structure" within the rhabdomeres not too unlike the vertebrate retinal rods and cones (2,7,12,14). We have, from the electron microscopic and pigment studies of a variety of photoreceptors, hypothesized a general geometrical fine structure for a photoreceptor in which the pigment molecules are oriented as monolayers at the aqueous protein and lipoprotein interfaces and are complexed with proteins or lipoproteins (12-14). In addition, Drosophila exhibits orientation relative to the direction of vibration of polarized light. The sensitivity to plane polarized light suggests the existence of a polarized light analyzer within the eye (9,