The Nature of the Retinal Action Potential, and the Spectral Sensitivities of Ultraviolet and Green Receptor Systems of the Compound Eye of the Worker Honeybee

1. The retinal action potential consists principally of a sustained negative wave which persists for as long as the stimulus. Transitory negative on-effects and off-effects may also be present, particularly at long wave lengths (green, yellow, and red) and in the light-adapted eye. 2. Only the maintained component of the potential can be elicited under CO2 anesthesia. The transient components are reversibly eliminated from the response at about the same time as the background noise of nerve and muscle spikes. It is suggested that the sustained component arises from the receptor cells, and the other components from second and higher order neurons. 3. The compound eye does not contain a homogeneous population of receptors. A green receptor system (maximum sensitivity at about 535 mµ) determines the response of the dark-adapted eye throughout most of the spectrum; during adaptation to yellow light, however, an ultraviolet receptor system is revealed, with maximum sensitivity at about 345 mµ. The anatomical bases of these receptor systems are unknown; however, they include both retinula cells and neurons in the optic ganglion. 4. There is no change in spectral sensitivity (Purkinje shift) in the first three logarithmic units above the threshold of the retinal action potential. 5. The relatively great effectiveness of near ultraviolet light in stimulating the positive phototaxis of the bee does not depend on excitation of the ultraviolet receptor of the ocellus.

[1]  E. Dodt,et al.  Die Spektralsensitivität von Insekten-Komplexaugen im Ultraviolett bis 290 mμ , 1959 .

[2]  Philip Ruck,et al.  A comparison of the electrical responses of compound eyes and dorsal ocelli in four insect species , 1958 .

[3]  T. Goldsmith ON THE VISUAL SYSTEM OF THE BEE (APIS MELLIFERA) , 1958, Annals of the New York Academy of Sciences.

[4]  T. Goldsmith,et al.  THE SPECTRAL SENSITIVITIES OF THE DORSAL OCELLI OF COCKROACHES AND HONEYBEES , 1958, The Journal of general physiology.

[5]  T. Goldsmith THE VISUAL SYSTEM OF THE HONEYBEE. , 1958, Proceedings of the National Academy of Sciences of the United States of America.

[6]  W. T. Catton,et al.  Electrical responses to visual stimulation in the optic lobes of the locust and certain other insects , 1956, The Journal of physiology.

[7]  G. Wald,et al.  The participation of different types of cones in human light and dark adaptation. , 1955, American journal of ophthalmology.

[8]  T. Jahn,et al.  ALLOCATION OF ELECTRICAL RESPONSES FROM THE COMPOUND EYE OF GRASSHOPPERS , 1942, The Journal of general physiology.

[9]  B. Ephrussi,et al.  A Technique of Transplantation for Drosophila , 1936, The American Naturalist.

[10]  W. Stiles COLOR VISION: THE APPROACH THROUGH INCREMENT-THRESHOLD SENSITIVITY. , 1959 .

[11]  P. Ruck The electrical responses of dorsal ocelli in cockroaches and grasshoppers , 1957 .

[12]  E F MACNICHOL,et al.  The peripheral origin of nervous activity in the visual system. , 1952, Cold Spring Harbor symposia on quantitative biology.

[13]  H. Autrum,et al.  Die Verschmelzungsfrequenzen des Bienenauges , 1950 .

[14]  C. Bernhard ISOLATION OF RETINAL AND OPTIC GANGLION RESPONSE IN THE EYE OF DYTISCUS , 1942 .

[15]  L. Bertholf Reactions of the Honeybee to Light , 1931 .

[16]  K. Frisch Der Farbensinn und Formensinn der Biene , 1914 .