Skip to main content
The Journal of General Physiology logoLink to The Journal of General Physiology
. 1975 Apr 1;65(4):399–419. doi: 10.1085/jgp.65.4.399

Action spectra and chromatic mechanisms of cells in the median ocelli of dragonflies

PMCID: PMC2214924  PMID: 1151320

Abstract

Spectral sensitivities were recorded intracellulary in median ocelli of Anax junius, Aeschnatuberculifera, and Libellulapulcella. All cells had peak sensitivities at 360 and 500 nm while UV-blue+green cells found only in Anax had a third peak sensitivity at 440 nm. Ratios of UV-to- green sensitivities varied from cell to cell in each ocellus, but no UV- only or green-only cells were recorded. Half of the cells tested had a reverse Purkinje shift: They were more sensitive in the green at low illuminations but more sensitive in the UV at high illuminations; their intensity-response curves at 370 and 520 nm crossed but became parallel for large responses. Wave-lengths 420 nm and shorter elicited a family of low intensity-response curves with one slope; wavelengths 440 nm and longer elicities a family of curves with another slope. Orange-adapting lights selectively adapted sensitivity in the green, but UV-adapting lights had little selective effect. Amounts of log-selective adaptation were proportional to log orange-adapting intensity. It is concluded that two spectral mechanisms can be recorded from each cell, possibly by coupling of UV and green cells or possibly because each cell contains two visual pigments. Selective chromatic adaptations may provide the ocellus with a kind of "authomatic color control," while the reverse Purkinje shift could extend the ocellus' sensitivity to prevailing skylight.

Full Text

The Full Text of this article is available as a PDF (1.5 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Brown J. E., Murray J. R., Smith T. G. Photoelectric potential from photoreceptor cells in ventral eye of Limulus. Science. 1967 Nov 3;158(3801):665–666. doi: 10.1126/science.158.3801.665. [DOI] [PubMed] [Google Scholar]
  2. Chappell R. L., Dowling J. E. Neural organization of the median ocellus of the dragonfly. I. Intracellular electrical activity. J Gen Physiol. 1972 Aug;60(2):121–147. doi: 10.1085/jgp.60.2.121. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. DARTNALL H. J. A. The interpretation of spectral sensitivity curves. Br Med Bull. 1953;9(1):24–30. doi: 10.1093/oxfordjournals.bmb.a074302. [DOI] [PubMed] [Google Scholar]
  4. DeVoe R. D. Dual sensitivities of cells in wolf spider eyes at ultraviolet and visible wavelengths of light. J Gen Physiol. 1972 Mar;59(3):247–269. doi: 10.1085/jgp.59.3.247. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. DeVoe R. D., Small R. J., Zvargulis J. E. Spectral sensitivities of wolf spider eyes. J Gen Physiol. 1969 Jul;54(1):1–32. doi: 10.1085/jgp.54.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. GOLDSMITH T. H., RUCK P. R. The spectral sensitivities of the dorsal ocelli of cockroaches and honeybees; an electrophysiological study. J Gen Physiol. 1958 Jul 20;41(6):1171–1185. doi: 10.1085/jgp.41.6.1171. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. GOLDSMITH T. H. The nature of the retinal action potential, and the spectral sensitivities of ultraviolet and green receptor systems of the compound eye of the worker honey-bee. J Gen Physiol. 1960 Mar;43:775–799. doi: 10.1085/jgp.43.4.775. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Nolte J., Brown J. E. Electrophysiological properties of cells in the median ocellus of Limulus. J Gen Physiol. 1972 Feb;59(2):167–185. doi: 10.1085/jgp.59.2.167. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Nolte J., Brown J. E., Smith T. G., Jr A hyperpolarizing component of the receptor potential in the median ocellus of Limulus. Science. 1968 Nov 8;162(3854):677–679. doi: 10.1126/science.162.3854.677. [DOI] [PubMed] [Google Scholar]
  10. Nolte J., Brown J. E. The spectral sensitivities of single cells in the median ocellus of Limulus. J Gen Physiol. 1969 Nov;54(5):636–649. doi: 10.1085/jgp.54.5.636. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Nolte J., Brown J. E. Ultraviolet-induced sensitivity to visible light in ultraviolet receptors of Limulus. J Gen Physiol. 1972 Feb;59(2):186–200. doi: 10.1085/jgp.59.2.186. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Ruck P. The Components of the Visual System of a Dragonfly. J Gen Physiol. 1965 Nov 1;49(2):289–307. doi: 10.1085/jgp.49.2.289. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Shaw S. R. Interreceptor coupling in ommatidia of drone honeybee and locust compound eyes. Vision Res. 1969 Sep;9(9):999–1029. doi: 10.1016/0042-6989(69)90044-3. [DOI] [PubMed] [Google Scholar]
  14. Smith T. G., Baumann F. The functional organization within the ommatidium of the lateral eye of limulus. Prog Brain Res. 1969;31:313–349. doi: 10.1016/S0079-6123(08)63248-3. [DOI] [PubMed] [Google Scholar]
  15. Zenkin G. M., Pigarev I. N. Zritel'no obuslovlennaia aktivnost' v sheinoi nervnoi tsepochke strekozy. Biofizika. 1971 Mar-Apr;16(2):299–306. [PubMed] [Google Scholar]

Articles from The Journal of General Physiology are provided here courtesy of The Rockefeller University Press

RESOURCES