Scotopic Range Research Articles

A Sensor Designed to Record Underwater Irradiance with Concern for a Shark's Spectral Sensitivity.

To ascertain how scalloped hammerhead sharks make nightly migrations to their feeding grounds as many as 20 km from their daytime abode, a seamount, a sensor was developed that measured irradiance intensity within the spectral range and sensitivity of the vision of the species. Could the sharks guide their movements by sensing the polarity of irradiation energy radiated from the sun or moon that penetrated into the oceanic depths? Two sensory receptors, cones and rods, are present in the retina of sharks to enable them to see both during daytime and nighttime. The peak sensitivity of the cones is red-shifted due to the presence of these wavelengths during the former period, while their response is linear under the range of the high light levels also present at this time; the peak sensitivity of rods is blue-shifted due to the presence of these wavelengths during dawn, dusk, and nighttime and is linear over the complementary range of low light levels. Spectral response curves for these two receptors were determined for sharks, and an attempt was made to match those of the sensors to the shark’s wavelength perception. The first sensor was matched to the photopic range using a photocell covered with a red-shifted gel filter; the second was matched to the scotopic range using a blue-shifted gel filter.

Determination of scotopic and photopic conventional visual acuity and hyperacuity.

Visual acuity (VA) is an important determinant of visual function. Here we establish procedures and recommendations for VA testing extending beyond the classical VA and thus make them available for future studies of visual function in health and disease. Specifically, we provide reference values for photopic and scotopic conventional uncrowded visual acuity (cVA) and Vernier-hyperacuity (hVA) and assess their reproducibility and dependence on contrast polarity. For ten observers with normal vision, we determined photopic ("p"; maximal luminance 220 cd/m2) and scotopic ("s"; maximal luminance 0.004 cd/m2; 40 min of dark adaptation) cVA and hVA, for two contrast polarities i.e. black optotypes on white background and vice versa. To assess intersession effects, two sets of measurements were obtained on different days. Compared to pcVA (1.32 decimal VA; - 0.12 ± 0.02 LogMAR), the phVA (14.45 decimal VA; - 1.16 ± 0.04 LogMAR) scaled (in terms of decimal visual acuity) on average with a factor 11.0, the scVA (0.12 decimal VA; 0.91 ± 0.03 LogMAR) with a factor of 0.1, and the shVA (1.47 decimal VA; - 0.17 ± 0.02 LogMAR) with a factor of 1.1. There were neither significant effects of contrast polarity (p > 0.12), nor of session (p > 0.28). Our approach optimises integrated photopic and scotopic cVA and hVA measurements for general use and thus encourages the integration of these important measures of scotopic visual function in future studies. The absence of strong intersession effects demonstrates that no dedicated training session is needed to obtain scotopic and hVA measurements. The combined measures of scotopic and photopic VAs open a field of applications to study interplay and plasticity of the retinal photoreceptor systems and cortical processing in health and visual disease. As a rule of thumb, hyperacuity is 10× higher both in the photopic and scotopic range than conventional acuity. Thus, scotopic hyperacuity is close to photopic conventional acuity.

CIE colour appearance models: A current perspective

This paper reviews CIE colour appearance models over the last three decades. It is divided into three stages: pre-1997, between 1997 and 2002 and post 2002. Before 1997, a number of colour appearance models were developed and experimental psychophysical datasets were accumulated to aid the development of these models and help with their verification. In 1997, CIECAM97s was the first model formally recommended by CIE. In 2002, CIECAM02 was recommended, a refinement of CIECAM97s. These models were limited to related colours of approximately two degrees, viewed under photopic conditions. Since that time work has progressed to develop a comprehensive colour appearance model to include the prediction of correlates of colour appearance over the photopic to scotopic range, the variation of stimulus size, the appearance of unrelated colours – light sources – and a uniform colour space to allow the calculation of colour difference in appearance space.

Calcium spike-mediated digital signaling increases glutamate output at the visual threshold of retinal bipolar cells.

Most retinal bipolar cells (BCs) transmit visual input from photoreceptors to ganglion cells using graded potentials, but some also generate calcium or sodium spikes. Sodium spikes are thought to increase temporal precision of light-evoked BC signaling; however, the role of calcium spikes in BCs is not fully understood. Here we studied how calcium spikes and graded responses mediate neurotransmitter release from Mb-type BCs, known to produce both. In dark-adapted goldfish retinal slices, light induced spikes in 40% of the axon terminals of intact Mbs; in the rest, light generated graded responses. These light-evoked membrane potentials were used to depolarize axotomized Mb terminals where depolarization-evoked calcium current (ICa) and consequent exocytosis-associated membrane capacitance increases (ΔCm) could be precisely measured. When evoked by identical dim light intensities, spiking responses transferred more calcium (Q(Ca)) and triggered larger exocytosis with higher efficiency (ΔCm/Q(Ca)) than graded potentials. Q(Ca) was translated into exocytosis linearly when transferred with spikes and supralinearly when transferred with graded responses. At the Mb output (ΔCm), spiking responses coded light intensity with numbers and amplitude whereas graded responses coded with amplitude, duration, and steepness. Importantly, spiking responses saturated exocytosis within scotopic range but graded potentials did not. We propose that calcium spikes in Mbs increase signal input-output ratio by boosting Mb glutamate release at threshold intensities. Therefore, spiking Mb responses are suitable to transfer low-light-intensity signals to ganglion cells with higher gain, whereas graded potentials signal for light over a wider range of intensities at the Mb output.

Does darkness limit the use of tree cavities for nesting by birds?

AbstractTree cavities are usually superabundant, and offer the safest nest sites. However, not all bird species utilize them. One of the reasons could be insufficient illumination in such places. As no visual system can operate in complete darkness, some nest cavities may be too dark to be usable even by cavity nesters, and some species may not have sufficient visual sensitivity to make use of dark cavities. So, presumably, light conditions could constrain both the evolution of the cavity-nesting habit and the selection of the nest site by the cavity-nesting birds. However, due to a paucity of data on light conditions in cavities, these suggestions have not been investigated to date. To provide more information on illumination inside tree cavities, we took measurements inside the nest cavities of Collared FlycatchersFicedula albicollisbreeding in a primeval forest (Białowieża National Park, Poland). Illuminance inside cavities was recorded at daybreak, just after the parents commenced feeding nestlings. We found that only ca. 4 % of incoming light reached the nest level, and birds could adjust light conditions inside cavities by placing their nests closer to smaller entrances. Illuminance at nests (median = 0.05 lx) fell within the mesopic–scotopic range of vertebrate eyes. Measurements performed on a sunny, cloudless midday in a model cavity showed that illuminance strongly decreased with distance from the entrance. Our results indicate cavities are always dark places where colour vision is usually impaired or absent and the “lighting” requirements of cavity nesters can affect their use of tree cavities. We discuss the implications of the findings for understanding the adaptations of cavity nesting in birds.

Masked excitatory crosstalk between the ON and OFF visual pathways in the mammalian retina

A fundamental organizing feature of the visual system is the segregation of ON and OFF responses into parallel streams to signal light increment and decrement. However, we found that blockade of GABAergic inhibition unmasks robust ON responses in OFF α-ganglion cells (α-GCs). These ON responses had the same centre-mediated structure as the classic OFF responses of OFF α-GCs, but were abolished following disruption of the ON pathway with L-AP4. Experiments showed that both GABA(A) and GABA(C) receptors are involved in the masking inhibition of this ON response, located at presynaptic inhibitory synapses on bipolar cell axon terminals and possibly amacrine cell dendrites. Since the dendrites of OFF α-GCs are not positioned to receive excitatory inputs from ON bipolar cell axon terminals in sublamina-b of the inner plexiform layer (IPL), we investigated the possibility that gap junction-mediated electrical synapses made with neighbouring amacrine cells form the avenue for reception of ON signals. We found that the application of gap junction blockers eliminated the unmasked ON responses in OFF α-GCs, while the classic OFF responses remained. Furthermore, we found that amacrine cells coupled to OFF α-GCs display processes in both sublaminae of the IPL, thus forming a plausible substrate for the reception and delivery of ON signals to OFF α-GCs. Finally, using a multielectrode array, we found that masked ON and OFF signals are displayed by over one-third of ganglion cells in the rabbit and mouse retinas, suggesting that masked crossover excitation is a widespread phenomenon in the inner mammalian retina.

Mesopic luminance assessed with minimum motion photometry

We measured the relative contribution of rods and cones to luminance across a range of photopic, mesopic, and scotopic adaptation levels and at various retinal eccentricities. We isolated the luminance channel by setting motion-based luminance nulls (minimum motion photometry) using annular stimuli. Luminance nulls between differently colored stimuli require equality in a weighted sum of rod and cone excitations. The relative cone weight increases smoothly from the scotopic range, where rods dominate, to photopic levels, where rod influence becomes negligible. The change from rod to cone vision does not occur uniformly over the visual field. The more peripheral the stimulus location, the higher is the light level required for cones to participate strongly. The relative cone contribution can be described by a sigmoid function of intensity, with two parameters that each depend on the eccentricity and spatial frequency of the stimulus. One parameter determines the "meso-mesopic" luminance--the center of the mesopic range, at which rod and cone contributions are balanced. This increases with eccentricity, reflecting an increase in the meso-mesopic luminance from 0.04 scotopic cd/m(2) at 2° eccentricity to 0.44 scotopic cd/m(2) at 18°. The second parameter represents the slope of the log-log threshold-versus-intensity curve (TVI curve) for rod vision. This parameter inversely scales the width of the mesopic range and increases only slightly with eccentricity (from 0.73 at 2° to 0.78 for vision at 18° off-axis).

Histamine Reduces Flash Sensitivity of ON Ganglion Cells in the Primate Retina

PURPOSE. In Old World primates, the retina receives input from histaminergic neurons in the posterior hypothalamus. They are a subset of the neurons that project throughout the central nervous system and fire maximally during the day. The contribution of these neurons to vision, was examined by applying histamine to a dark-adapted, superfused baboon eye cup preparation while making extracellular recordings from peripheral retinal ganglion cells. METHODS. The stimuli were 5-ms, 560-nm, weak, full-field flashes in the low scotopic range. Ganglion cells with sustained and transient ON responses and two cell types with OFF responses were distinguished; their responses were recorded with a 16-channel microelectrode array. RESULTS. Low micromolar doses of histamine decreased the rate of maintained firing and the light sensitivity of ON ganglion cells. Both sustained and transient ON cells responded similarly to histamine. There were no statistically significant effects of histamine in a more limited study of OFF ganglion cells. The response latencies of ON cells were approximately 5 ms slower, on average, when histamine was present. Histamine also reduced the signal-to-noise ratio of ON cells, particularly in those cells with a histamine-induced increase in maintained activity. CONCLUSIONS. A major action of histamine released from retinopetal axons under dark-adapted conditions, when rod signals dominate the response, is to reduce the sensitivity of ON ganglion cells to light flashes. These findings may relate to reports that humans are less sensitive to light stimuli in the scotopic range during the day, when histamine release in the retina is expected to be at its maximum.

Contrast Sensitivity of Cats and Humans in Scotopic and Mesopic Conditions

Human contrast sensitivity in low scotopic conditions is regulated according to the deVries-Rose law. Previous cat behavioral data, as well as cat and mice electrophysiological data, have not confirmed this relationship. To resolve this discrepancy at the behavioral level, we compared sensitivity in dim light for cats and humans in parallel experiments using the same visual stimuli and similar behavioral paradigms. Both species had to detect Gabor functions (SD = 1.5 degrees, spatial frequencies from 0 to 4 cpd, temporal frequency 4 Hz) presented 8 degrees to the right or left of a central fixation point over an 8 log-unit range of adaptation levels spanning scotopic vision and extending well into the mesopic range. Cats had 0.74 log unit greater absolute sensitivity than that of humans for spatial frequencies <or=1/8 cpd. Cats had better contrast sensitivity overall for spatial frequencies <1/2 cpd, whereas humans were more sensitive for spatial frequencies above this. However, most of the cat's sensitivity advantage for low spatial frequencies could be accounted for by the greater light-concentrating abilities of its optics. Contrast sensitivity to 4 cpd was poor or absent in the scotopic range for both species. For both, scotopic increment thresholds were proportional to the square root of retinal illuminance, in accordance with the deVries-Rose law. Overall, cat and human visual systems appear to operate under very similar constraints for rod vision, including the regulation of contrast sensitivity across adaptation levels. A companion paper compares sensitivity of neurons in the lateral geniculate nucleus to these behavioral data.

Analysis of Ocular Hypopigmentation inRab38cht/chtMice

To characterize the ocular phenotype resulting from mutation of Rab38, a candidate gene for Hermansky-Pudlak syndrome. Chocolate mice (cht, Rab38(cht/cht)) and control heterozygous (Rab38(cht/)(+)) and wild-type mice were examined clinically, histologically, ultrastructurally, and electrophysiologically. Mice homozygous for both the Rab38(cht) and the Tyrp1(b) alleles were similarly examined. Rab38(cht/cht) mice showed variable peripheral iris transillumination defects at 2 months of age. Patches of RPE hypopigmentation were noted clinically in 57% of Rab38(cht/cht) eyes and 6% of Rab38(cht/)(+) eyes. Rab38(cht/cht) mice exhibited thinning of the iris and RPE and larger b-wave amplitudes in the scotopic range when compared with the control animals. Compared with wild-type mice, Rab38(cht/cht) melanosomes were smaller and there were fewer in neuroectodermally derived retinal pigment epithelium; in neural crest-derived choroid melanocytes, they were smaller in size only. Mutation of both Rab38 and Tyrp1 produced mice with ocular and coat color pigment dilution greater than that seen with either mutation alone. Comprehensive clinical and pathologic analyses showed no other organ system or blood defects in Rab38(cht/cht) mice. Rab38(cht/cht) mice show ocular characteristics reminiscent of human oculocutaneous albinism, as well as iris and RPE thinning. The synergistic effects of the Rab38(cht) and Tyrp1(b) alleles suggest that TYRP1 is not the only target of RAB38 trafficking. This mouse line provides a useful model for studying melanosome biology and its role in human ocular diseases.

The integration window for shape cues is a function of ambient illumination

Minimal discrete shape cues, i.e., dots that marked positions on the outer boundary of namable objects, were divided into two subsets, which were shown very quickly with a variable delay between subsets. Recognition of a given object required integration of the information provided by the two subsets, and previous research had found that recognition declined as the delay between subsets was increased. The present experiment found the decline in recognition to be linear for each of several levels of ambient illumination, dropping rapidly under photopic test conditions, and with the slope being progressively less steep with transition into the scotopic range. The change in the duration of information persistence may be related to the density of information that is provided under various lighting conditions, and a requirement that the information be buffered against noise or "packaged" to accommodate successive saccades.

Use of a digital infrared pupillometer to assess patient suitability for refractive surgery

Purpose To assess the role of binocular infrared dynamic pupillometry in measuring and recording the pupil size in scotopic, low mesopic, and high mesopic illumination prior to refractive surgery. Setting The Rosen Eye Surgery Centre, Alexandra Hospital Victoria Park, Manchester, United Kingdom. Methods In this prospective study, the pupil sizes of 58 patients (mean age 46 years ± 11.7 [SD]) presenting for refractive surgery assessment were evaluated using the P2000 SA pupillometer (Procyon Instruments Ltd.). Each patient was measured at 3 illumination levels: 0.02 lux (scotopic), 0.15 lux (low mesopic), and 10.6 lux (high mesopic). At each level, 10 images were acquired by the system at 5 images per second. Both eyes were imaged at the same time, with a spatial accuracy of 0.03 mm per pixel. Results Pupillary unrest (PU) occurred at all levels of illumination. Some degree of PU amplitude was observed in both eyes of all patients. The median PU was 0.12 mm (95% confidence limits [CLs], 0.11, 0.14) in the scotopic range, 0.34 mm (95% CLs, 0.28, 0.38) in the low mesopic range, and 0.28 mm (95% CLs, 0.23, 0.30) in the high mesopic range. The degree of anisocoria varied among individuals. The median value was 0.28 mm (95% CLs, 0.21, 0.39) in the scotopic range, 0.32 mm (95% CLs, 0.26, 0.37) in the low mesopic range, and 0.16 mm (95% CLs, 0.12, 0.19) in the high mesopic range. Because of PU and anisocoria, single versus multiple binocular measurements demonstrated the possibility of errors greater than 1.0 mm in some patients. Conclusions Patients showed an appreciable degree of pupillary motion during measurement at all levels of illumination; the motion was largest under low mesopic illumination. The 2 pupils were rarely identical. Multiple-measurement binocular pupillometry is better than single monocular measurement to gain a precise description of pupil behavior before refractive surgery.

The Piéron function in the threshold region.

The Piéron function (Piéron, 1914, 1920, 1952) describes the decay of reaction time (RT) when the intensity of the stimulus is increased. It is generally demonstrated within a suprathreshold range of intensities. However, in some studies, for the lowest range of intensities, the exponent of the function is clearly greater than that for the upper ranges of intensities. Such an increase in the exponent for the lowest intensities is assumed to result from a combined effect of stimulus intensity and of stimulis uncertainty in detection. Our first experiment used luminance levels that covered all the scotopic range and a spatial two-alternative forced-choice task in which both accuracy and RT were measured. It demonstrated a drastic increase in the exponent in the Piéron function when the intensities reached the threshold region. Since the estimates of the threshold region may have been biased by the use of a much larger range of luminances, a second experiment was conducted using luminances that covered only the threshold region. This experiment confirmed the previous estimates for the threshold region.

Sensitivity and dynamics of rod signals in H1 horizontal cells of the macaque monkey retina.

We measured the sensitivity, temporal frequency response, latency, and receptive field diameter of rod input to the H1 horizontal cell type in an in vitro preparation of the macaque retina. The H1 cell has both a cone-connected dendritic tree and a long axon-like process that terminates in a rod-connected arbor. We recorded from the H1 cell body where rod signals were distinguished by sensitivity to short wavelength light after dark adaptation. Receptive fields of rod vs. cone mediated responses were coextensive, indicating that the rod signal is transmitted via rod–cone gap junctions. Sensitivity of the H1 cell rod signal was ∼1 log unit higher than that of the cone signal. Below cone threshold rod signals were temporally low-pass, with a cutoff frequency below 10 Hz. Rod signals became faster and more transient with increasing light levels. We conclude that the H1 cell rod signal is not sensitive in the low scotopic range and, by comparison with the rod signal recorded directly in cones (Schneeweis & Schnapf (1995) Science, 268, 1053–1056), signal transmission across the cone-H1 synapse does not significantly filter the temporal properties of the rod signal.

Spatial and temporal properties of cat horizontal cells after prolonged dark adaptation

We studied the change of spatial and temporal response properties for cat horizontal (H-) cells during prolonged dark adaptation. H-cell responses were recorded intracellularly in the optically intact, in vivo eye. Spatial and temporal properties were first measured for light-adapted H-cells, followed by a period of dark adaptation, after which the same measurements were repeated. During dark adaptation threshold sensitivity was measured at regular intervals. Stable, long lasting recordings allowed us to measure changes of sensitivity and receptive field characteristics for adaptation periods up to 45 min. Although cat H-cells showed no signs of dark suppression or light sensitization, they remained insensitive in the scotopic range, even after prolonged dark adaptation. Absolute thresholds were in the low mesopic range. The sensitization was brought about by a shift from cone to rod input, and by substantial increases of both spatial and temporal integration upon dark adaptation. The length constant in the light-adapted state was on average about 4 deg. After dark adaptation it was up to a factor of three larger, with a median ratio of 1.85. Response delays, latencies and durations for (equal amplitude) threshold flash responses substantially increased during dark adaptation.

Regulation of melatonin production and intracellular calcium concentrations in the trout pineal organ.

The present in vitro study correlates measurements of the melatonin production from trout pineal organs with those of the intracellular calcium concentration in pinealocytes. Melatonin production increases with decreasing irradiance and shows maximal values in darkness. Some pinealocytes exhibit spontaneous calcium oscillations, although most of them have a stable basal calcium concentration. Diminishing extracellular calcium and enhancing magnesium reduces melatonin release in the light-and dark-adapted state. The application of Co2+ decreases melatonin secretion in the mesopic and scotopic range, reversibly blocks spontaneous calcium oscillations, reduces the basal intracellular calcium concentration in non-oscillating pinealocytes, and inhibits the KCl-induced rise in intracellular calcium. Application of glutamate, norepinephrine, isoproterenol, or dopamine has no significant effect on melatonin secretion. Norepinephrine does not influence the calcium concentration in any of the trout pinealocytes. Treatment with the GABAA-receptor agonist muscimol causes a slight reduction of melatonin release in the mesopic and scotopic range of illumination, without affecting intracellular calcium concentrations. Thus, Co2+ and low calcium/high magnesium buffer reduce melatonin release through an action on the calcium concentration in trout pinealocytes and not through a blockade of synaptic transmission. All the data show that the trout pineal organ synthesizes and releases melatonin in relation to the irradiance of the incident light and that neuronal inputs have a minor, if any, influence on melatonin synthesis.

Temporal summation for grating patches detected at low light levels.

It is not known if temporal integration for periodic stimuli is affected by changes in scotopic luminance. Contrast thresholds were measured as a function of duration for 0.25 cpd grating patches across a 2.3 log-unit scotopic range. Threshold vs. duration (TVD) functions were identical in shape regardless of mean luminance once scaled by translating along log-log axes. Critical duration decreased 0.09 log-units per log-unit increase in retinal illuminance. This slope is identical to that reported for photopic conditions, suggesting that temporal integration may be determined by the same neural pathway at all light levels.

Acuity-sensitivity trade-offs of X and Y cells in the cat lateral geniculate complex: role of the medial interlaminar nucleus in scotopic vision.

1. The cat medial interlaminar nucleus (MIN) receives inputs almost exclusively from tapetal retina, suggesting that the MIN has a special role in dim-light vision. In this study we compared the sensitivities of cells in the MIN with those in layers A and magnocellular C of the lateral geniculate nucleus (LGNd), using drifting sinusoidal gratings to determine contrast thresholds as a function of spatial frequency and retinal adaptation level over the entire scotopic range. 2. About one-half of the cells recorded in the MIN and layer A had brisk responses that could be nulled by properly positioned, counterphased sinusoidal gratings, and were classified as X cells. The rest of the cells in the MIN and layer A, as well as all cells recorded in layer C, were Y cells. 3. MIN cells had higher contrast sensitivity than layer A cells for low spatial frequencies (0.15 cycles/deg and below) over a wide range of adaptation levels, both overall and for separate comparisons within X or Y cells. Layer C Y cells were intermediate in sensitivity between MIN and layer A Y cells. For low spatial frequencies, Y cells as a group were more sensitive than X cells, whereas the reverse was true for high spatial frequencies. 4. These data enable one to determine the lowest adaptation level at which stimuli of a given contrast can be detected for a given structure. At the lowest spatial frequencies, the MIN can function at adaptation levels approximately 1 log unit below layer A, averaged over all stimulus contrasts. In contrast, the tapetum lowers luminance threshold by at most 0.16 log unit. 5. For scotopic conditions and eccentricities within 15 degrees of the area centralis, contrast sensitivity decreases with eccentricity for low spatial frequencies and remains flat or slightly increases for high spatial frequencies. This relationship, which is opposite to that found for photopic vision, is strongest for MIN Y cells. 6. These data support the hypothesis that the retinal conflict between sensitivity and acuity is ameliorated in the CNS through separate thalamic relays with different degrees of afferent convergence. MIN cells have higher luminance sensitivity than layer A cells, but at the expense of acuity. Layer C appears to occupy an intermediate position in this trade-off.

Non-linear spatial summation in cat retinal ganglion cells at different background levels

Cat retinal ganglion cells were identified as X-cells (linear) or Y-cells (non-linear) on the basis of the spatial summation properties of their receptive fields. For each cell, the degree of non-linearity in spatial summation was assessed at a number of different mean luminance levels in order to determine how spatial linearity depended on mean luminance. The stimuli were counterphase sinusoidal gratings whose contrast was sinusoidally modulated in time. A grating with one bar centered on the receptive field was used to measure the contrast sensitivity of the mechanisms which produced responses at the stimulus frequency. A grating with a zero crossing centered on the receptive field was used to measure the contrast sensitivity of mechanisms responsible for the non-linear frequency doubled responses of Y-cells. As the mean luminance was reduced from low photopic to scotopic, the contrast sensitivity decreased for both the linear and non-linear responses. The ratio of non-linear to linear sensitivity in Y-cells changed less with background than did either contrast sensitivity. In some Y-cells this ratio decreased slightly at low luminance levels, but in others it did not. X-cells appeared to sum signals linearly at all levels of illumination. X-cells and Y-cells could still be distinguished on the basis of their spatial summation properties in the scotopic range.

Studies of visual function and its decay in mice with hereditary retinal degeneration.

Functional implications of mouse hereditary retinal degeneration have been studied at the level of the superior colliculus and visual cortex in the C57BL/6J-le rd strain. On autoradiography at a light-microscopic level, following eye injection with radioactive compounds, central visual structures appeared normal. A slight reduction in ipsilateral retinal projection was probably related to reduced retinal pigmentation associated with the light ear (le) mutation. In recordings from visual cortex and tectum in rd mice older than five months the cells discharged with highly rhythmic maintained activity. This ongoing activity depended on retinal input, since temporary asphyxia of the eye stopped it immediately. The frequency of the rhythm was influenced by the anesthesia. In these older mice no visual receptive fields could be mapped, but in a few tectal recordings it was possible to suppress the maintained activity by diffuse, very intense illumination. As in normal mice, no auditory or somatosensory responses were observed in the visual cortex or upper tectal layers. In recordings from tectum before the age of three weeks retinotopic topography and receptive fields were normal. By day 24 no receptive fields could be recorded from parts of the tectum representing the central 90--100 degrees of the visual field, whereas within a peripheral ring responses were still roughly normal under photopic conditions. Over the following four months these peripheral responses faded away slowly. Incremental thresholds, especially in the scotopic range, were elevated, rising slowly to unmeasurable values. Similarly during dark adaptation the thresholds fell to values several log units above those reached in normal mice; these values of dark adapted thresholds in rd mice rose with age. This is consistent with morphological changes known to occur in the retina as a consequence, of the rd mutation the rods degenerating before the cones.