Adaptation in the Compound Eye and Interaction with Screening Pigment

1972 ◽  
Vol 56 (1) ◽  
pp. 119-128
Author(s):  
U. YINON
Keyword(s):  
Dark Adaptation ◽  
Light Adaptation ◽  
Compound Eye ◽  
Electrical Response ◽  
Negative Potential ◽  
Neural Pathways ◽  
Photochemical Process ◽  
Screening Pigment ◽  
The Difference ◽  
Adaptation Processes

The electroretinogram pattern in the compound eye of T. molitor and the appearance of irregular small potentials and spikes superimposed on the ERG are influenced during dark and light adaptation procedures. The amplitude of the principal negative potential reflects bleaching and recovery of the photochemical process. This is not true for the latency values. The delay of the electrical response increases in the dark and decreases in the light adapted eye. These changes were influenced by the intensity of the adapting light. Mutant eyes only lack screening pigment and have normal visual neural pathways. The absence of this pigment lowered the threshold sensitivity of the unscreened eye in dark adaptation. The difference between the adaptation processes in mutants and normal animals has been suggested as a criterion for measuring the net effect of the screening pigment in the compound eye.

Changes of Acuity during Light and Dark Adaptation in the Dragonfly Compound Eye

1990 ◽  
Vol 45 (1-2) ◽  
pp. 137-142 ◽  
Author(s):  
Eric J. Warrant ◽  
Robert B. Pinter
Keyword(s):  
Dark Adaptation ◽  
Time Course ◽  
Light Adaptation ◽  
Compound Eye ◽  
Sensitivity Function ◽  
The State ◽  
Intracellular Recordings ◽  
Acceptance Angle ◽  
Angular Sensitivity ◽  
Rapid Reduction

Abstract Intracellular recordings of angular sensitivity from the photoreceptors of Aeschnid dragonflies (Hemianax papuensis and Aeschna brevistyla) are used to determine the magnitude and time course of acuity changes following alterations of the state of light or dark adaptation. Acuity is defined on the basis of the acceptance angle, Δρ (the half-width of the angular-sensitivity function). The maximally light-adapted value of Δρ is half the dark-adapted value, indicating greater acuity during light adaptation. Following a change from light to dark adaptation, Δρ increases slowly, requiring at least 3 min to reach its dark-adapted value. In contrast, the reverse change (dark to light) induces a rapid reduction of Δρ , and at maximal adapting luminances, this reduction takes place in less than 10 sec.

Investigation of the Screening Pigment System in the Compound Eye of the Moth Agrotis segetum (fam. Noctuidae) by Visible Reflectometry

1987 ◽  
Vol 42 (1-2) ◽  
pp. 152-156 ◽  
Author(s):  
Trond Nordtug ◽  
Thor Bernt Melø
Keyword(s):  
Light Adaptation ◽  
Compound Eye ◽  
Extinction Spectrum ◽  
Light Extinction ◽  
Agrotis Segetum ◽  
Lag Phase ◽  
Reflection Spectroscopy ◽  
Screening Pigment ◽  
Reflected Light ◽  
Superposition Eye

Abstract The functional properties of the light adaptation system in the superposition eye of the moth Agrotis segetum have been investigated by reflection spectroscopy. The spectrum of the reflected light from the tapetum of dark adapted eyes had a peak at about 580 nm corresponding to a spacing between the reflecting layers in the tapetum of 145 nm. During light adaptation of the eye the observed reflectance changes could be explained by light extinction in one screening pigment. The shape of the extinction spectrum of the screening was constant throughout the adaptation process and after a lag phase the optical density of the pigment in the light path increased linearly with time. The screening pigment caused light extinction both by absorption and to some degree also by scattering. The absorption spectrum of the screening pigment had a broad maximum about 590 nm and the scattering efficiency of the pigment particles seemed to be nearly independent of the wavelength.

scholarly journals The Eye Muscle of Calliphora Vomitoria L

1973 ◽  
Vol 58 (3) ◽  
pp. 565-583
Author(s):  
JOHN PATTERSON
Keyword(s):  
Dark Adaptation ◽  
Light Adaptation ◽  
Interspike Interval ◽  
Compound Eye ◽  
Optic Lobe ◽  
Visual Images ◽  
Eye Muscle ◽  
Calliphora Erythrocephala ◽  
Spontaneous Movements ◽  
Anatomical Arrangement

1. A muscle attached to the medial edge of the compound eye is described for the blowfly Calliphora vomitoria. 2. Electrophysiological activity in the form of continuous tonically firing potentials can be recorded extracellularly from the muscle. These potentials are generated by the muscle and have the same origin as the ‘clock-spikes’ recorded previously from the optic lobe of Calliphora erythrocephala. 3. The interspike interval of the eye muscle potentials varies inversely with the ambient temperature. 4. Light-adaptation results in a decrease and dark-adaptation an increase in the resting interspike interval of the eye-muscle potentials. 5. Light-adaptation is correlated with increase and dark-adaptation with decrease in the depth of the compound eye as measured at the insertion of the muscle. 6. The pseudopupil produced by illumination of the compound eye from the inside displays spontaneous movements which can be correlated with the anatomical arrangement and spontaneous activity of the eye muscle. 7. The probable function of spontaneous and transient changes in eye-muscle activity is to promote scanning of the visual images produced by the dioptrics of the compound eye.

Depth related variation in the structure and functioning of the compound eye of the Norway lobster Nephrops norvegicus

1990 ◽  
Vol 70 (2) ◽  
pp. 343-355 ◽  
Author(s):  
E. Gaten ◽  
P.M.J. Shelton ◽  
C.J. Chapman ◽  
A.M. Shanks
Keyword(s):  
Deep Water ◽  
Dark Adaptation ◽  
Compound Eye ◽  
Light Exposure ◽  
Retinula Cell ◽  
Nephrops Norvegicus ◽  
Norway Lobster ◽  
Photon Fluence Rate ◽  
Screening Pigment ◽  
Photon Fluence

The mobility and quantity of retinula cell proximal screening pigment, and the liability of the eyes to light-induced damage, were investigated in the Norway lobster, Nephrops norvegicus (L.), obtained from three separate populations from depths of 18, 75, and 135 m.During the morning after capture, the migration of the proximal pigment in response to the onset of illumination below the threshold for damage varied between the three populations. In the eyes of deep water N. norvegicus, the proximal screening pigment was located close to or below the basement membrane when dark-adapted and rose to a position midway up the rhabdoms when light-adapted. In the dark-adapted N. norvegicus from shallow water the proximal pigment was located more distally than in eyes of deep water animals. After the onset of illumination, the pigment migrated distally to completely cover the rhabdoms. The amount of retinula cell proximal screening pigment was found to decrease linearly with depth.When dark-adapted individuals from each depth were exposed to light a positive correlation was obtained between the photon fluence rate (PER) and the proportion of the retina damaged. For a given light exposure the amount of damage was highest in animals from deeper water. The PFR causing 25% damage was approximately 1 log unit higher in animals from 18 m compared to those from 135 m.The amount of damage varied with the delay between capture of the animals and exposure to light. When exposed 2 h after capture significant differences between depths were seen but the results were influenced by the incomplete dark adaptation of some specimens.

scholarly journals DARK ADAPTATION IN AGRIOLIMAX

1928 ◽  
Vol 12 (1) ◽  
pp. 83-109 ◽  
Author(s):  
W. J. Crozier ◽  
Ernst Wolf
Keyword(s):  
Dark Adaptation ◽  
Light Adaptation ◽  
The Body ◽  
Differential Sensitivity ◽  
Different Types ◽  
The Difference ◽  
Two Sides ◽  
Kinetics Of ◽  
Different Levels ◽  
Continuous Excitation

A method is described which measures the excitation of Agriolimax by light, during the progress of light adaptation, by assuming that the orientating effect of continuous excitation is expressed as a directly proportionate tension difference in the orienting muscles of the two sides of the body. The tendency toward establishment of such a tension difference is caused to work against a similar geotropic effect at right angles to the phototropic one. This enables one to study the kinetics of light adaptation, and of dark adaptation as well. The situation in the receptors is adequately described by the paradigm See PDF for Equation similar to that derived by Hecht for the differential sensitivity of various forms, but with the difference that the "dark" reaction is not only "bimolecular" but also autocatalysed by the reaction product S. The progress of dark adaptation is reflected (1) in the recovery of the amplitude of the orientation and (2) in the rates of light adaptation at different levels of the recovery; each independently supports these assumptions, for which the necessary equations have been provided. These equations also account for the relative variabilities of the angles of orientation, and, more significantly, for the two quite different kinds of curves of dark adaptation which are obtained in slightly different types of tests.

Dark-adaptation processes in the rhodopsin rods of the frog's retina

1967 ◽  
Vol 7 (1-2) ◽  
pp. 17-41 ◽  
Author(s):  
K.O. Donner ◽  
Tom Reuter
Keyword(s):  
Dark Adaptation ◽  
Adaptation Processes

The Cockroach DCMD Neurone: I. Lateral Inhibition and the Effects of Light- and Dark-adaptation

1982 ◽  
Vol 99 (1) ◽  
pp. 61-90 ◽  
Author(s):  
DONALD H. EDWARDS
Keyword(s):  
Lateral Inhibition ◽  
Dark Adaptation ◽  
Light Adaptation ◽  
Absolute Intensity ◽  
Recurrent Network ◽  
Light Spot ◽  
Movement Detector ◽  
Threshold Response ◽  
Inhibitory Network ◽  
Local Background

1. The responses of the cockroach descending contralateral movement detector (DCMD) neurone to moving light stimuli were studied under both light- and dark-adapted conditions. 2. With light-adaptation the response of the DCMD to two moving 2° (diam.) spots of white light is less than the response to a single spot when the two spots are separated by less than 10° (Fig. 2). 3. With light-adaptation the response of the DCMD to a single moving light spot is a sigmoidally shaped function of the logarithm of the light intensity (Fig. 3a). With dark-adaptation the response of a DCMD to a single moving light spot is a bell-shaped function of the logarithm of the stimulus intensity (Fig. 3b). The absolute intensity that evokes a threshold response is about one-and-a-half log units less in the dark-adapted eye than in the light-adapted eye. 4. The decrease in the DCMD's response that occurs when two stimuli are closer than 10°, and when a single bright stimulus is made brighter, indicates that lateral inhibition operates among the afferents to the DCMD. 5. It is shown that this inhibition cannot be produced by a recurrent lateral inhibitory network. A model of the afferent path that contains a non-recurrent lateral inhibitory network can account for the response/intensity plots of the DCMD recorded under both light-adapted and dark-adapted conditions. 6. The threshold intensity of the DCMD is increased if a stationary pattern of light is present near the path of the moving spot stimulus. This is shown to be due to a peripheral tonic lateral inhibition that is distinct from the non-recurrent lateral inhibition described earlier. 7. It is suggested that the peripheral lateral inhibition acts to adjust the threshold of afferents to local background light levels, while the proximal non-recurrent network acts to enhance the acuity of the eye to small objects in the visual field, and to filter out whole-field stimuli.

Diurnal changes in retinula cell sensitivities and receptive fields (two-dimensional angular sensitivity functions) in the apposition eyes of Ligia exotica (Crustacea, Isopoda)

2001 ◽  
Vol 204 (2) ◽  
pp. 239-248 ◽  
Author(s):  
T. Hariyama ◽  
V.B. Meyer-Rochow ◽  
T. Kawauchi ◽  
Y. Takaku ◽  
Y. Tsukahara
Keyword(s):  
Receptive Fields ◽  
Resolving Power ◽  
Pigment Cells ◽  
Diurnal Changes ◽  
Two Dimensional ◽  
Angular Sensitivity ◽  
Pigment Granules ◽  
Screening Pigment ◽  
The Difference ◽  
Night And Day

The structural organization of the retinula cells in the eye of Ligia exotica changes diurnally. At night, the microvilli elongate, losing the regular and parallel alignment characteristic of the day condition. Crystalline cones and distal rhabdom tips are not pushed into each other during the day, but at night the rhabdoms protrude into the crystalline cones by up to 5 microm. Screening pigment granules in the retinula cells disperse during the night, but migrate radially towards the vicinity of the rhabdom during the day. No such displacements of the pigment granules of either distal or proximal screening pigment cells were observed. The sensitivity of the eye, monitored by electroretinogram (ERG) recordings, changes diurnally: values at midnight are, on average, 10 times those occurring during the day. However, intracellular recordings from single retinula cells (50 during the day and 50 at night) indicate that the difference between night and day sensitivities is only 2.5-fold. Two-dimensional angular sensitivity curves, indicative of a single unit's spatial sensitivity, had considerably less regular outlines at night than during the day. If based on the 50 % sensitivity level, day and night eyes possessed receptive fields of almost identical width (approximately 2 degrees), but if sensitivities below the 50 % limit were included, then receptive fields at night were significantly more extensive. We suggest that the morphological adaptations and diurnal changes in chromophore content seen in the apposition eye of L. exotica allow this animal to improve its photon capture at night while preserving at least some of the spatial resolving power characteristic of the light-adapted state. This would explain why this animal is capable of performing complex escape behaviours in the presence of predators both in bright and in very dim light.

The Effect of Changed Extracellular Calcium and Sodium Concentration on the Electroretinogram of the Crayfish Retina

1980 ◽  
Vol 35 (3-4) ◽  
pp. 308-318 ◽  
Author(s):  
H. Stieve ◽  
I. Claßen-Linke
Keyword(s):  
Dark Adaptation ◽  
Time Course ◽  
Calcium Concentration ◽  
Light Adaptation ◽  
Sodium Concentration ◽  
Strong Increase ◽  
Calcium Stores ◽  
Half Time ◽  
Astacus Leptodactylus ◽  
External Calcium

Abstract The electroretinogram (ERG) of the isolated retina of the crayfish Astacus leptodactylus evoked by strong 10 ms light flashes at constant 5 min intervals was measured while the retina was continuously superfused with various salines which differed in Ca2+ -and Na+ -concentrations. The osmotic pressure of test- and reference-saline was adjusted to be identical by adding sucrose. Results: 1. Upon raising the calcium-concentration of the superfusate in the range of 20-150 mmol/l (constant Na+ -concentration: 208 mmol/l) the peak amplitude hmax and the half time of decay t2 of the ERG both decrease gradually up to about 50% in respect to the corresponding value in reference saline. 2. The recovery of the ERG due to dark adaptation following the “weakly light adapted state” is greatly diminished in high external [Ca2+]ex. 3. Lowering the external calcium-concentration (10 →1 mmol/l) causes a small increase in hmax and a strong increase of the half time of decay t2 (about 180%). Upon lowering the calcium concentration of the superfusate to about 1 nmol/l by 1 mmol/l of the calcium buffer EDTA, a slowly augmenting diminution of the ERG height hm SLX occurs. How­ever, a strong retardation of the falling phase of the ERG characterized by an increase in t2 occurs quickly. Even after 90 min stay in the low calcium saline the retina is still not inexcitable; hmax is 5 - 10% of the reference value. The diminution of hmax occurs about six-fold faster when the buffer concentration is raised to 10 mmol/l EDTA. 4. Additional lowering of the Na+ -concentration (208 →20.8 mmol/l) in a superfusate with a calcium concentration raised to 150 mmol/l causes a strong reduction of the ERG amplitude hmax to about 10%. 5. In a superfusate containing 1 nmol/l calcium such lowering of the sodium concentration (208 → 20.8 mmol/l) causes a diminution of the ERG height to about 40% and the shape of the ERG to become polyphasic; at least two maxima with different time to peak values are observed. Interpretation: 1. The similarity of effects, namely raising external calcium concentration and light adaptation on the one hand and lowering external calcium and dark adaptation on the other hand may indicate that the external calcium is acting on the adaptation mechanism of the photoreceptor cells, presumably by influencing the intracellular [Ca2+]. 2. The great tolerance of the retina against Ca2+ -deficiency in the superfusate might be effected by calcium stores in the retina which need high Ca2+ -buffer concentrations in the superfusate to become exhausted. 3. In contrast to the Limulus ventral nerve photoreceptor there does not seem to be an antagonis­ tic effect of sodium and calcium in the crayfish retina on the control of the light channels. 4. The crayfish receptor potential seems to be composed of at least two different processes. Lowering calcium-and lowering external sodium-concentration both diminish the height and change the time course of the two components to a different degree. This could be caused by in­ fluencing the state of adaptation and thereby making the two maxima separately visible.

Sign in / Sign up

Export Citation Format

Share Document