Biomedical subjects

P Lennie

Publications and source records attributed to P Lennie.

At least 19 recordsLinked to original sources

PubMed2001

Information conveyed by onset transients in responses of striate cortical neurons.

Normal eye movements ensure that the visual world is seen episodically, as a series of often stationary images. In this paper we characterize the responses of neurons in striate cortex to stationary grating patterns presented with abrupt onset. These responses are distinctive. In most neurons the onset of a grating gives rise to a transient discharge that decays with a time constant of 100 msec or less. The early stages of response have higher contrast gain and higher response gain than later stages. Moreover, the variability of discharge during the onset transient is disproportionately low. These factors together make the onset transient an information-rich component of response, such that the detectability and discriminability of stationary gratings grows rapidly to an early peak, within 150 msec of the onset of the response in most neurons. The orientation selectivity of neurons estimated from the first 150 msec of discharge to a stationary grating is indistinguishable from the orientation selectivity estimated from longer segments of discharge to moving gratings. Moving gratings are ultimately more detectable than stationary ones, because responses to the former are continuously renewed. The principal characteristics of the response of a neuron to a stationary grating-the initial high discharge rate, which decays rapidly, and the change of contrast gain with time-are well captured by a model in which each excitatory synaptic event leads to an immediate reduction in synaptic gain, from which recovery is slow.

Action Potentials↗

PubMed2001

Packing arrangement of the three cone classes in primate retina.

We describe a detailed analysis of the spatial arrangement of L, M and S cones in the living eyes of two humans and one monkey. We analyze the cone mosaics near 1 degrees eccentricity using statistical methods that characterize the arrangement of each type of cone in the mosaic of photoreceptors. In all eyes, the M and L cones are arranged randomly. This gives rise to patches containing cones of a single type. In human, but not in monkey, the arrangement of S-cones cannot be distinguished from random.

Animals↗

PubMed2001

Importance of color in the segmentation of variegated surfaces.

We examined how variations in color and brightness are used by the visual system in distinguishing textured surfaces that differed in their first- or second-order statistics. Observers viewed a 32 x 32 array containing two types of square elements differing in chromaticity or luminance or both. The spatial distributions of the two kinds of elements were varied within the array until observers could distinguish two juxtaposed regions. At low but not at high contrast, observers are better able to distinguish regions when the elements differ only in chromaticity than when they differ only in luminance. The advantage of color at low contrasts results from the greater visibility of the arrays defined by color variation. An observer's capacity to distinguish textures defined by variations in first-order chromatic statistics is little affected by the addition of achromatic noise but is more affected by the addition of chromatic noise. The relative robustness of chromatic cues in the face of achromatic noise leaves the visual system well equipped to exploit color variations in segmenting complex scenes, even in the presence of variations in brightness. This capacity seems to depend on mechanisms that sum over large regions: When surfaces differ in their second-order statistics and cannot be distinguished by mechanisms that sum over large regions, the advantage of color is much diminished.

Artifacts↗

PubMed2000

Color vision: putting it together.

Color vision depends on the visual system comparing signals that originate in different classes of cone photoreceptors. New work shows that the different classes of cones are not only distributed irregularly, but in different individuals they are present in very variable proportions. Surprisingly, this does not affect color vision.

Animals↗

PubMed2000

Fine structure of parvocellular receptive fields in the primate fovea revealed by laser interferometry.

Optical blurring in the eye prevents conventional physiological techniques from revealing the fine structure of the small parvocellular receptive fields in the primate fovea in vivo. We explored the organization of receptive fields in macaque parvocellular lateral geniculate nucleus cells by using sinusoidal interference fringes formed directly on the retina to measure spatial frequency tuning at different orientations. Most parvocellular cells in and near the fovea respond reliably to spatial frequencies up to and beyond 100 cycles/ degrees of visual angle, implying center input arising mainly from a single cone. Temporal frequency and contrast response characteristics were also measured at spatial frequencies up to 130 cycles/degrees. We compared our spatial frequency data with the frequency responses of model receptive fields that estimate the number, configuration, and weights of cones that feed the center and surround. On the basis of these comparisons, we infer possible underlying circuits. Most cells had irregular spatial frequency-response curves that imply center input from more than one cone. The measured responses are consistent with a single cone center together with weak input from nearby cones. By exposing a fine structure that cannot be discerned by conventional techniques, interferometry allows functional measurements of the early neural mechanisms in spatial vision.

Animals↗

PubMed1999

Rapid adaptation in visual cortex to the structure of images.

Complex cells in striate cortex of macaque showed a rapid pattern-specific adaptation. Adaptation made cells more sensitive to orientation change near the adapting orientation. It reduced correlations among the responses of populations of cells, thereby increasing the information transmitted by each action potential. These changes were brought about by brief exposures to stationary patterns, on the time scale of a single fixation. Thus, if successive fixations expose neurons' receptive fields to images with similar but not identical structure, adaptation will remove correlations and improve discriminability.

Action Potentials↗

PubMed1998

Visual processing levels revealed by response latencies to changes in different visual attributes.

Visual latencies, and their variation with stimulus attributes, can provide information about the level in the visual system at which different attributes of the image are analysed, and decisions about them made. A change in the colour, structure or movement of a visual stimulus brings about a highly reproducible transient constriction of the pupil that probably depends on visual cortical mechanisms. We measured this transient response to changes in several attributes of visual stimuli, and also measured manual reaction times to the same stimulus changes. Through analysis of latencies, we hoped to establish whether changes in different stimulus attributes were processed by mechanisms at the same or different levels in the visual pathway. Pupil responses to a change in spatial structure or colour are almost identical, but both are ca. 40 ms slower than those to a change in light flux, which are thought to depend largely on subcortical pathways. Manual reaction times to a change in spatial structure or colour, or to the onset of coherent movement, differ reliably, and all are longer than the reaction time to a change in light flux. On average, observers take 184 ms to detect a change in light flux, 6 ms more to detect the onset of a grating, 30 ms more to detect a change in colour, and 37 ms more to detect the onset of coherent motion. The pattern of latency variation for pupil responses and reaction times suggests that the mechanisms that trigger the responses lie at different levels in cortex. Given our present knowledge of visual cortical organization, the long reaction time to the change in motion is surprising. The range of reaction times across different stimuli is consistent with decisions about the onset of a grating being made in V1 and decisions about the change in colour or change in motion being made in V4.

Adult↗

PubMed1998

Single units and visual cortical organization.

The visual system has a parallel and hierarchical organization, evident at every stage from the retina onwards. Although the general benefits of parallel and hierarchical organization in the visual system are easily understood, it has not been easy to discern the function of the visual cortical modules. I explore the view that striate cortex segregates information about different attributes of the image, and dispatches it for analysis to different extrastriate areas. I argue that visual cortex does not undertake multiple relatively independent analyses of the image from which it assembles a unified representation that can be interrogated about the what and where of the world. Instead, occipital cortex is organized so that perceptually relevant information can be recovered at every level in the hierarchy, that information used in making decisions at one level is not passed on to the next level, and, with one rather special exception (area MT), through all stages of analysis all dimensions of the image remain intimately coupled in a retinotopic map. I then offer some explicit suggestions about the analyses undertaken by visual areas in occipital cortex, and conclude by examining some objections to the proposals.

Animals↗

PubMed1997

Mechanisms underlying segmentation of colored textures.

This paper examines the nature of the post-receptoral chromatic and achromatic mechanisms involved in a texture segmentation task. Observers viewed a 64 x 64 square-element texture in which the chromaticity and brightness of each element was drawn from a one-dimensional Gaussian distribution of values centered at a white point in color space. The orientation in color space and variance of this distribution defined the noise in the stimulus. The mean chromaticity and/or brightness of a central 32 x 32 element area (the target) was shifted away from the white point along the same direction as the noise or along a different direction. We measured target thresholds as a function of noise amplitude. The steepness of this relationship defined the effectiveness of the noise. Within planes spanned by the achromatic axis and one of the two cardinal chromatic axes, we found selective effects of noise along each of the two cardinal axes. Within the purely chromatic (isoluminant) plane, we found selective effects of noise along four lines--the two cardinal chromatic axes and two intermediate ones. We describe a simple model to account for our results.

Color Perception↗

PubMed1997

Color search and visual field segregation.

Visual search for targets that combine color and shape features that are shared by distracting items can be conducted spatially in parallel. Experimental results show that parallel search for color/shape conjunctions is possible when the shapes chosen let observers segregate the spatially interspersed items into figure and ground and when, within the figure, the target differs from other items by a distinguishing color feature. Results of experiments that manipulate stimulus color suggest that adaptive mechanisms of color discrimination are used to detect targets within such a figure.

Color Perception↗

PubMed1996

Spatio-temporal requirements for binocular correlation in stereopsis.

We measured sensitivity to binocular correlation in dynamic random-dot stereograms that defined moving sinusoidal gratings-in-depth. At a range of spatial frequencies and drift rates we established sensitivity by adding Gaussian distributed disparity noise to the modulation of disparity that defined a cyclopean grating, and finding the noise amplitude that rendered the grating just detectable. This permitted correlation thresholds to be measured at a range of suprathreshold disparity amplitudes. Spatial requirements for binocular correlation depend little on temporal frequency, and vice versa. This suggests that binocular correlation mechanisms can be characterized by independent spatial and temporal sensitivity functions. The temporal frequency function has a low pass characteristic. Sensitivity declines above about 1 c/sec, reaching its limit at 4-8 c/sec. The spatial characteristic depends greatly on the amplitude of disparity modulation, changing from band pass at low amplitude to low pass at high amplitude. The maximum resolvable spatial frequency is 4-6 c/deg, but declines sharply for relatively high amplitudes. The interaction between amplitude and spatial frequency cannot be explained by fixed high or low limits on detectable disparity gradients.

Depth Perception↗

PubMed1994

Ganglion cell pathways for rod vision.

Measurements of the acuity of rod vision made by two different techniques show it to vary only slightly with eccentricity. At eccentricities beyond 15 deg acuity is well predicted from the sampling properties of the mosaic of the P-class of ganglion cells. With decreasing eccentricity acuity falls progressively below the sampling limit of P-cells, but even at the lowest eccentricity examined (5 deg) does not reach the limit imposed by the sampling properties of the mosaic of M-cells. At an eccentricity of 5 deg rod vision could be supported by as few as 20% of P-cells.

Dark Adaptation↗

PubMed1993

Luminance.

Luminance was introduced by the CIE as a photometric analog of radiance. This implies that an additive spectral-luminosity function characterizes the human observer. In practice, many different spectral-sensitivity functions characterize human vision, although few produce the additive spectral-luminosity function V (lambda), which is suitable for use in practical photometry. Methods that give rise to additive spectral-sensitivity functions that most resemble V (lambda) tend to have in common the use of spatial or temporal frequencies that will discriminate against signals from the short-wavelength-sensitive cone pathways or against signals in other chromatic pathways. Some of the difference among results obtained with different techniques seems to reflect the extent to which the methods can bring about changes in the state of chromatic adaptation, but it also seems likely that not all tasks tap the same postreceptoral mechanisms. Psychophysical evidence is equivocal regarding the nature of the postreceptoral mechanisms: some evidence suggests just three mechanisms, one of which has a spectral sensitivity that is like V (lambda); other evidence suggests the existence of multiple mechanisms with different spectral sensitivities. Physiological recordings from neurons in the macaque's visual pathway suggest that the properties of the magnocellular system may be sufficient to account for spectral-sensitivity functions measured with the techniques of heterochromatic flicker photometry, minimally distinct border, and critical flicker fusion. These are the psychophysical methods that yield spectral sensitivities that are most like V (lambda). Other methods of measuring spectral sensitivity seem more likely to depend on signals that travel through the parvocellular system.

Color Perception↗

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↗