Abstract
Intracellular recordings have been made of responses to step, ramp and sinusoidal changes of light by second-order L-neurones and a third-order neurone, DNI, of locust (Locusta migratoria) ocelli.
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1.
The membrane potential at the peak response by an L-neurone to a change in light is proportional to the light increment or decrement, independent of background, over a range of at least 4 log units. As background increases, response latency and time-course decrease, and responses become more phasic (Fig. 1).
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2.
Adaptation to a changed mean light level involves a change in sensitivity and a slow change in resting membrane potential, which never adapts completely to dark resting potential in the presence of light (Fig. 3).
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3.
L-neurones can follow changes in light which last several seconds, but responses to fast changes are enhanced in amplitude (Figs. 4, 5). An increase in background light causes an increase in the frequency of sinusoidally modulated light at which the largest response occurs (Fig. 4).
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4.
The responses of DNI to increased light saturate at lower intensities than those of L-neurones. During adaptation to different background light intensities, there is no change in the input-output relation of the synapse between an L-neurone and DNI (Figs. 6, 7).
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5.
For a rapid decrease in light, DNI produces a rebound spike, followed by a period of silence (Figs. 5, 8).
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References
Ammermüller J, Zettler F (1986) Time- and voltage-dependent currents in locust ocellar L-neurones. J Comp Physiol A 159:363–376
Autrum H, Zettler F, Jährvilehto M (1970) Postsynaptic potentials from a single monopolar neuron of the ganglion opticum I of the blowfly Calliphora. Z Vergl Physiol 70:414–425
Baader A (1989) Sensitivity of ocellar interneurons of the honeybee to constant and temporally modulated light. J Neurobiol 20:519–529
Bacon J, Möhl B (1983) The tritocerebral commissure giant (TCG) wind-sensitive interneurone in the locust. J Comp Physiol 150:439–452
Chappell RL, Dowling JE (1972) Neural organization of the median ocellus of the dragonfly. I. Intracellular electrical activity. J Gen Physiol 60:121–147
Dubs A (1981) Non-linearity and light adaptation in the fly photo-receptor. J Comp Physiol 144:53–59
Fuortes MGF, Hodgkin AL (1964) Changes in time scale and sensitivity in the ommatidia of Limulus. J Physiol (Lond) 172:239–263
Goodman CS (1976) Anatomy of the ocellar neurones of acridid grasshoppers. I. The large interneurones. Cell Tissue Res 175:203–225
Griss C, Rowell CHF (1986) Three descending interneurons reporting deviation from course in the locust. I. Anatomy. J Comp Physiol A 158:765–774
Hayashi JH, Moore JW, Stuart AE (1985) Adaptation in the inputoutput relation of the synapse made by the barnacle photoreceptor. J Physiol (Lond) 368:175–195
Hensler K (1992) Intracellular recordings from intact locusts flying under closed-loop visual conditions. J Exp Biol 168:301–306
Laughlin SB (1973) Neural integration in the first optic neuropile of dragonflies. I. Signal amplification in a dark adapted second order neuron. J Comp Physiol 84:335–355
Laughlin SB (1989) The role of sensory adaptation in the retina. J Exp Biol 146:39–62
Laughlin SB, Hardie RC (1978) Common strategies for light adaptation in the peripheral visual systems of fly and dragonfly. J Comp Physiol 128:319–340
Laughlin SB, Howard J, Blakeslee B (1987) Synaptic limitations to contrast coding in the retina of the blowfly Calliphora. Proc R Soc (Lond) B 231:437–467
Mizunami M (1990) Nonlinear signal transmission between secondand third-order neurons of cockroach ocelli. J Gen Physiol 95:297–317
Mizunami M, Tateda H (1986) Classification of ocellar interneurones in the cockroach brain. J Exp Biol 125:57–70
Mizunami M, Tateda H, Naka K-I (1986) Dynamics of cockroach ocellar neurons. J Gen Physiol 88:275–292
Mizunami M, Yamashita S, Tateda H (1987) Calcium-dependent action potentials in the second-order neurones of cockroach ocelli. J Exp Biol 130:259–274
Normann RA, Perlman I (1979) The effects of background illumination on the photoresponses of red and green cones. J Physiol (Lond) 286:491–507
Osorio D (1986) Directionally selective cells in the locust medulla. J Comp Physiol A 159:841–847
Osorio D (1991) Mechanisms of early visual processing in the medulla of the locust optic lobe: How self-inhibition, spatial pooling and signal rectification contribute to the properties of transient cells. Visual Neurosci 7:345–355
Patterson JA, Goodman LJ (1974) Intracellular responses of receptor cells and second order cells of the ocelli of the locust Schistocerca gregaria. J Comp Physiol 95:237–250
Pinter RB (1972) Frequency and time domain properties of retinular cells of the desert locust (Schistocerca gregaria) and the house cricket (Acheta domesticus). J Comp Physiol 77:383–397
Reichert H, Rowell CHF (1985) Integration of nonphaselocked exteroceptive information in the control of rhythmic flight in the locust. J Neurophysiol 53:1201–1218
Rowell CHF, Pearson KG (1983) Ocellar input to the flight motor system of the locust: structure and function. J Exp Biol 103:265–288
Rowell CHF, Reichert H (1986) Three descending interneurons reporting deviation from course in the locust. II. Physiology. J Comp Physiol A 158:775–794
Shaw SR (1984) Early visual processing in insects. J Exp Biol 112:225–251
Simmons PJ (1980) A locust wind and ocellar brain neurone. J Exp Biol 85:281–294
Simmons PJ (1981) Synaptic transmission between second- and third-order neurones of a locust ocellus. J Comp Physiol 147:401–414
Simmons PJ (1982) The operation of connexions between photoreceptors and large second-order neurones in dragonfly ocelli. J Comp Physiol 149:389–398
Simmons PJ (1985) Postsynaptic potentials of limited duration in visual neurones of the locust. J Exp Biol 117:193–213
Simmons PJ (1990) The processing of information in neurones of the simple eyes of an insect. In: Guthrie DM (ed) Higher order sensory processing. Manchester University Press, Manchester, pp 8–26
Simmons PJ, Hardie RC (1988) Evidence that histamine is a neurotransmitter of photoreceptors in the locust ocellus. J Exp Biol 138:205–219
Simmons PJ, Littlewood PMH (1989) Structure of a tonically transmitting synapse between identified interneurones in the locust brain. J Comp Neurol 283:129–142
Strausfeld NJ (1976) Atlas of an insect brain. Springer, Berlin Heidelberg New York
Taylor CP (1981) Contribution of compound eyes and ocelli to steering of locust flight. I. Behavioural analysis. J Exp Biol 93:1–18
Wilson M (1975) Autonomous pigment migration in the radial pupil of locust ocelli. Nature (Lond) 258:603–604
Wilson M (1978) The functional organisation of locust ocelli. J Comp Physiol 124:297–316
Wilson M (1978) Generation of graded potential signals in the second order cells of locust ocellus. J Comp Physiol 124:317–331
Wilson M (1978) The origin and properties of discrete hyperpolarising potentials in the second order cells of the locust ocellus.J Comp Physiol 128:347–358
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Simmons, P.J. Adaptation and responses to changes in illumination by second- and third-order neurones of locust ocelli. J Comp Physiol A 173, 635–648 (1993). https://doi.org/10.1007/BF00197771
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DOI: https://doi.org/10.1007/BF00197771