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P Lennie

Publications and source records attributed to P Lennie.

At least 19 recordsLinked to original sources
PubMed1992

Chromatic adaptation to natural and incandescent illuminants.

A color CRT image display system was used to present adapting backgrounds that were spatially and temporally varied. Three observers adjusted the chromaticity of test stimuli to produce an achromatic appearance under a variety of adapting conditions. The achromatic-appearing chromaticities were used as measures of the observers' states of chromatic adaptation. The spatial configuration of the adapting background was varied to measure the spatial extent of the mechanisms responsible for chromatic adaptation. The temporal configuration of the adapting background was varied to measure the time-course of these mechanisms. The results show that chromatic adaptation is spatially localized with a time-course on the order of 10 sec. Since the mechanisms were shown to be spatially localized, the observed temporal integration across eye movements is required to allow these mechanisms to adjust to the spatially integrated scene chromaticity.

Adaptation, Ocular↗
PubMed1990

Coding of image contrast in central visual pathways of the macaque monkey.

Measurements of contrast sensitivity were obtained from isolated neurons in the lateral geniculate nucleus, striate cortex, and middle temporal visual area of macaque monkeys. Between the lateral geniculate nucleus and the middle temporal area contrast sensitivity functions become progressively steeper. Furthermore, many neurons in the middle temporal area are more sensitive than any cell encountered in early stages. Measurements made with stimuli of different sizes show that this high sensitivity depends on areal summation across the receptive field.

Action Potentials↗
PubMed1990

Chromatic mechanisms in striate cortex of macaque.

We measured the responses of 305 neurons in striate cortex to moving sinusoidal gratings modulated in chromaticity and luminance about a fixed white point. Stimuli were represented in a 3-dimensional color space defined by 2 chromatic axes and a third along which luminance varied. With rare exceptions the chromatic properties of cortical neurons were well described by a linear model in which the response of a cell is proportional to the sum (for complex cells, the rectified sum) of the signals from the 3 classes of cones. For each cell there is a vector passing through the white point along which modulation gives rise to a maximal response. The elevation (theta m) and azimuth (phi m) of this vector fully describe the chromatic properties of the cell. The linear model also describes neurons in l.g.n. (Derrington et al., 1984), so most neurons in striate cortex have the same chromatic selectivity as do neurons in l.g.n. However, the distributions of preferred vectors differed in cortex and l.g.n.: Most cortical neurons preferred modulation along vectors lying close to the achromatic axis and those showing overt chromatic opponency did not fall into the clearly defined chromatic groups seen in l.g.n. The neurons most responsive to chromatic modulation (found mainly in layers IVA, IVC beta, and VI) had poor orientation selectivity, and responded to chromatic modulation of a spatially uniform field at least as well as they did to any grating. We encountered neurons with band-pass spatial selectivity for chromatically modulated stimuli in layers II/III and VI. Most had complex receptive fields. Neurons in layer II/III did not fall into distinct groups according to their chromatic sensitivities, and the chromatic properties of neurons known to lie within regions rich in cytochrome oxidase appeared no different from those of neurons in the interstices. Six neurons, all of which resembled simple cells, showed unusually sharp chromatic selectivity.

Animals↗
PubMed1989

Contrast adaptation in striate cortex of macaque.

We have characterized the contrast-response relationships for simple and complex cells in striate cortex of macaque monkey, before and during adaptation to high-contrast sinusoidal gratings of the optimal spatial-frequency and orientation. Adaptation brings about systematic changes in the steepness of contrast-response curves and in the effective contrast of stimuli. Adaptation reduces the detectability of low-contrast gratings by almost a factor of three, but by extending the operating range of most cells it appears to improve the discriminability of high-contrast stimuli that previously gave rise to responses of saturating amplitude.

Adaptation, Ocular↗
PubMed1988

Mechanisms of color vision.

We review the physiological and psychophysical research on mechanisms of color vision. Psychophysical work has led to the formulation of explicit theories of the early stages of color vision. The principal postulates of these theories have been confirmed by physiologists (e.g., the existence of three classes of receptors and second-stage mechanisms in which the signals from these receptors are compared), but some important features of the psychophysical scheme have found limited physiological support. One such issue is the absence of the unitary "achromatic" mechanism required by psychophysicists. We know a good deal less about the chromatic analyses that occur beyond these early stages. Although physiologists have devoted much effort to the study of cortical mechanisms, little of this work has been guided by clear ideas of the tasks performed by them. The provision of color constancy and the ability to segment scenes are perhaps the foremost concerns of chromatic mechanisms, and recent psychophysical work bearing on these problems offers physiologists clearer guidance on what to seek with their electrodes.

Animals↗
PubMed1987

Detection latencies of X and Y type cells of the cat's dorsal lateral geniculate nucleus.

The latencies of visually-evoked responses from X- and Y-type neurons of the cat's dorsal lateral geniculate nucleus were measured in a manner that takes account of the inherent variability of discharge in these cells. Latencies measured in this way vary from trial to trial in one cell (and also between cells) by tens to as much as hundreds of milliseconds. This variability in the time for generation of reliable responses suggests that the much emphasized conduction advantage of the Y pathway plays a minor role in the detection of visual stimuli by the cat.

Animals↗
PubMed1986

Shared pathways for rod and cone vision.

We have used heterochromatic gratings falling on 10 deg temporal retina to measure the spatial contrast sensitivities of the isolated rod and cone systems in the mesopic range. As the level of illumination was raised within this range, the contrast sensitivity of the rod system increased, reaching a peak of about 50 (and providing an acuity of 6 c/deg) at 20 scot. td, whereupon the rod system began to saturate. Over most of the mesopic range the sensitivity of the cone system was lower than that of the rod system, although it provided better acuity (up to 15 c/deg). Within the range of spatial frequencies capable of exciting both rod and cone systems, a grating that excited only rods was indistinguishable from a grating of the same spatial frequency that excited only cones. Moreover, contrast adaptation to gratings that excited either rods or cones raised threshold for gratings that excited rods or cones. From these results we conclude that signals from rods and cones travel together in pathways subserving the detection of low spatial frequencies, while only signals from cones travel in pathways subserving the detection of high spatial frequencies.

Adaptation, Ocular↗
PubMed1986

Mechanisms of color constancy.

We develop a model of how the visual system finds the colors of objects that have unknown shapes and positions. The model relies on mechanisms of light adaptation, coupled with eye movements, to recover three descriptors of surface reflectance that are represented in the signals of an achromatic mechanism and two color-opponent mechanisms. These descriptors are transformed to yield estimates of hue, the dimension of surface color that is independent of object shape and viewing geometry.

Color↗
PubMed1979

The mechanism of peripherally evoked responses in retinal ganglion cells.

1. Responses to stimulation of retinal regions remote from the classical receptive field were recorded from optic tract fibres in lightly anaesthetized cats. 2. X- and Y-cells gave reliably different responses to the sudden reversal of the phase of a high contrast grating that fell on the retina more than 15 deg from the centre of the receptive field. 3. The mechanism that generates these responses ('shift effect' or 'periphery effect') in Y-cells is insensitive to the spatial phase of the stimulating grating. It can resolve gratings of higher spatial frequency than can be resolved by the classical receptive field mechanisms of Y-cells but its temporal resolution is poorer. 4. Signals that contribute to peripherally evoked responses are accumulated over a region that extends to at least 35 deg from the centre of the receptive field. Although this region is not uniformly sensitive, regions in the periphery of the visual field are as effective as regions around the area centralis in eliciting the responses, and do not require coarser gratings. 5. In some Y-cells the response to peripheral stimulation was amplified by increasing (on-centre units) or decreasing (off-centre units) the steady illumination of the centre of the receptive field. This confirms Krüger & Fisher (1973), but the effect is only found in a proportion of cells. 6. The mechanism that generates peripherally evoked responses is tentatively identified with the 'rectifying subunits' postulated by Hochstein & Shapley (1976b) to account for the spatial non-linearity in the receptive fields of Y-cells. Transient (bistratified) amacrine cells are known to have many of the properties attributed to these mechanisms (Chan & Naka, 1976).

Animals↗
PubMed1977

The effects of remote retinal stimulation on the responses of cat retinal ganglion cells.

1. Action potentials were recorded from optic nerve fibres of lightly anaesthetized cats while parts of the retina remote from the receptive field were stimulated by a shifting grating. 2. Vigorous responses can be obtained under these conditions, confirming McIlwain (1966), Krüger & Fischer (1973), and others. 3. These 'shift responses' are not caused by fluctuations of stray light because (a) they cannot be reduced by deliberately increasing or decreasing the light falling on the receptive field synchronously with the shifting grating; (b) a steady adapting light applied to the receptive field does not raise the threshold for the responses, whereas adapting light on the peripheral retina does, and (c) the threshold for the responses is elevated more following bleaching adaptation of the periphery than following bleaching adaptation of the centre. 4. Shift responses are strong, of short latency, and brief in duration in brisk-transient (Y-type) neurones. With few exceptions they are weak but long-lasting in brisk-sustained (X-type) neurones. 5. Shift responses are unlike responses from the main receptive field in having a distinct threshold; the magnitude of the response to weak gratings is not simply proportional to contrast, as is the case with weak stimuli applied to the receptive field. 6. It is thought that the excitatory pathway may involve amacrine cells, and that this mechanism may be concerned with the detection of the shifts of the image that occur with saccadic eye movements.

Action Potentials↗
PubMed1977

Cone signals in the cat's retina.

1. The discharges of ganglion cells in the cat's retina were recorded under conditions intended to isolate the cone system.2. Stiles' two-colour threshold technique permitted the photopic system to be studied when at its highest sensitivity. The absolute sensitivity of a ganglion cell, expressed in equivalent photons of lambda(max) at the cornea per impulse discharged, was about 2500 times less when driven by cones than when driven by rods. This ratio improves to around 200 when allowance is made for the much smaller fraction absorbed by cones of photons incident on the cornea.3. The number of extra impulses discharged in response to a brief flash was approximately proportional to the number of photons in the flash, up to a limit.4. There was a region in the middle of the receptive field within which the area of a test spot and its illumination for threshold varied inversely. A flash extending over the peripheral part of the receptive field raised threshold above its minimum, presumably as a result of surround antagonism. Assessed from area-threshold curves, the balance of centre-surround antagonism in the photopic receptive field did not seem to depend upon background illumination.5. The threshold for a small (0.2 degrees ) flash confined to the middle of the receptive field was independent of background illumination until the background exceeded a particular level, the ;dark light' (I(o)). In different units this ranged about a mean of 7.89 log photons (560 nm equivalent) deg(-2) sec(-1). For backgrounds that exceeded I(o), threshold followed approximately Weber's law up to the highest illuminations that could be produced.6. With test flashes that filled the centre of the receptive field, the Weber fraction (test flash illumination/background illumination) in some units fell below 1%.7. Changes in the time course and latency of response accompanied the changes in sensitivity caused by alterations in background illumination. Responses of both X- and Y-cells became more transient and faster.8. The loss of sensitivity to a test flash brought about by a steady background light depended upon the size of that light. Sensitivity varied inversely with background area within a central region that matched closely the summing area for test flashes.

Action Potentials↗
PubMed1977

Convergence of rod and cone signals in the cat's retina.

1. In an attempt to understand the convergence of rod and cone signals in the cat's retina, ganglion cells that received inputs from both rods and cones were stimulated using lights chosen to excite one or other receptor system or both together.2. If a mesopic background was chosen to allow the ganglion cell to be excited by a blue-green test flash primarily through rods and a deep red flash primarily through cones, one light could not be alternated with the other without eliciting a response from the cell.3. This appears to be a result of the different temporal properties of the scotopic and photopic systems. On the mesopic background responses to blue-green test flashes were transient. Responses to red test flashes arose with similar latency, but were more sustained.4. Rod and cone systems responded with similar latencies in the presence of the mesopic background that substantially light-adapted the rod system but left the full sensitivity of the cone system undiminished. When equivalently light-adapted, the cone system was faster.5. When brief flashes that acted through rods were presented with flashes that acted through cones the ganglion cell's response was the sum of the responses to the two flashes presented separately, as long as the flashes were weak. This linear relation ceased to hold when flashes were strong, but the breakdown appears not to be the result of mutual inhibition between rod and cone signals.6. When a background light excited both rod and cone systems it appeared to reduce sensitivity independently in each.7. The scotopic and photopic receptive fields of a given ganglion cell always were of the same type, on- or off-centre, and, within the limits of measurement, the central regions of the receptive fields were concentric and both the same size.

Action Potentials↗
PubMed1977

Rod-cone interaction in light adaptation.

1. The increment-threshold for a small test spot in the peripheral visual field was measured against backgrounds that were red or blue.2. When the background was a large uniform field, threshold over most of the scotopic range depended exactly upon the background's effect upon rods. This confirms Flamant & Stiles (1948). But when the background was small, threshold was elevated more by a long wave-length than a short wave-length background equated for its effect on rods.3. The influence of cones was explored in a further experiment. The scotopic increment-threshold was established for a short wave-length test spot on a large, short wave-length background. Then a steady red circular patch, conspicuous to cones, but below the increment-threshold for rod vision, was added to the background. When it was small, but not when it was large, this patch substantially raised the threshold for the test.4. When a similar experiment was made using, instead of a red patch, a short wave-length one that was conspicuous in rod vision, threshold varied similarly with patch size. These results support the notion that the influence of small backgrounds arises in some size-selective mechanism that is indifferent to the receptor system in which visual signals originate. Two corollaries of this hypothesis were tested in further experiments.5. A small patch was chosen so as to lift scotopic threshold substantially above its level on a uniform field. This threshold elevation persisted for minutes after extinction of the patch, but only when the patch was small. A large patch made bright enough to elevate threshold by as much as the small one gave rise to no corresponding after-effect.6. Increment-thresholds for a small red test spot, detected through cones, followed the same course whether a large uniform background was long- or short wave-length. When the background was small, threshold upon the short wave-length one began to rise for much lower levels of background illumination, suggesting the influence of rods. This was confirmed by repeating the experiment after a strong bleach when the cones, but not rods, had fully recovered their sensitivity. Increment-thresholds upon small backgrounds of long or short wave-lengths then followed the same course.

Adaptation, Ocular↗