Biomedical subjects

A B Poirson

Publications and source records attributed to A B Poirson.

7 recordsLinked to original sources

PubMed1997

Adaptation to contingencies in macaque primary visual cortex.

We tested the hypothesis that neurons in the primary visual cortex (V1) adapt selectively to contingencies in the attributes of visual stimuli. We recorded from single neurons in macaque V1 and measured the effects of adaptation either to the sum of two gratings (compound stimulus) or to the individual gratings. According to our hypothesis, there would be a component of adaptation that is specific to the compound stimulus. In a first series of experiments, the two gratings differed in orientation. One grating had optimal orientation and the other was orthogonal to it, and therefore did not activate the neuron under study. These experiments provided evidence in favour of our hypothesis. In most cells adaptation to the compound stimulus reduced responses to the compound stimulus more than it reduced responses to the optimal grating, and the responses to the compound stimulus were reduced more by adaptation to the compound stimulus than by adaptation to the individual gratings. This suggests that a component of adaptation was specific to (and caused by) the simultaneous presence of the two orientations in the compound stimulus. To test whether V1 neurons could adapt to other contingencies in the stimulus attributes, we performed a second series of experiments, in which the component gratings were parallel but differed in spatial frequency, and were both effective in activating the neuron under study. These experiments failed to reveal convincing contingent effects of adaptation, suggesting that neurons cannot adapt equally well to all types of contingency.

Adaptation, Ocular↗

PubMed1996

A video-input device that displays high-luminance, high-resolution color images.

We describe the design and performance of a bright, full-color, video-input display monitor that can produce image luminances as high as 50,000 cd/m2 for images 15 x 10 deg in size. We have constructed this device by rearranging the components of a commercially available projection television. Our display device allows an experimenter to evaluate human visual responses to complex spectro-spatio-temporal patterns presented at naturally occurring light levels.

Color Perception↗

PubMed1996

Pattern-color separable pathways predict sensitivity to simple colored patterns.

We have studied how contrast threshold sensitivity depends jointly on pattern and color. We measured sensitivity to colored Gabor patches from 0.5 to 8 c/deg. At each spatial frequency, we measured in many different color directions. We analyze the sensitivity measurements using a series of nested models. We conclude that a model consisting of three pattern-color separable mechanisms predicts detection performance nearly as well as fitting psychometric functions independently. We derive the pattern and color sensitivities of the separable mechanisms from the experimental data. Two derived mechanisms are spatially lowpass and spectrally color-opponent. The third mechanism is spatially bandpass and spectrally broadband.

Color Perception↗

PubMed1993

Appearance of colored patterns: pattern-color separability.

We have measured how color appearance of square-wave bars varies with stimulus strength and spatial frequency. Observers adjusted the color of a uniform patch to match the color appearance of the bars in square-wave patterns. We used low-to-moderate square-wave patterns, from 1 to 8 cycles per degree (c/deg). The matches are not photoreceptor matches but rather are established at more central neural sites. The signals at the putative central sites obey several simple regularities. The cone contrast of the uniform patch is proportional to square-wave stimulus strength (color homogeneity) and additive with respect to the superposition of equal-frequency square waves containing different colors (color superposition). We use the asymmetric matches to derive, from first principles, three pattern-color-separable appearance pathways. The matches are explained by two spectrally opponent, spatially low-pass mechanisms and one spectrally positive, spatially bandpass mechanism. The spectral mechanisms that we derive are similar to luminance and opponent mechanisms that are derived with entirely different experimental methods.

Color Perception↗

PubMed1990

The ellipsoidal representation of spectral sensitivity.

When plotted in three-dimensional color-space, thresholds of colored lights fall on or near the surface of an ellipsoid. Using data reported in the literature, we estimate the deviation between sets of spectral threshold measurements and the ellipsoid that passes closest to the data. Seventy-three percent of the reported spectral thresholds fall within 0.1 log units of the best-fitting ellipsoid. Our ability to distinguish one ellipsoidal fit as significantly better than another is limited by the choice of sampling directions in color-space. Spectral lights do not provide a good set of sampling directions for reducing the uncertainty about the estimated best-fitting ellipsoid. Complete characterization of visual sensitivity requires measuring thresholds to mixtures of spectral lights.

Color Perception↗

PubMed1990

Task-dependent color discrimination.

When an observer's ability to discriminate colored objects is estimated from the variability in color matches, the observer inspects adjacent visual fields carefully and makes considered judgments. Color discrimination does not always take place under such viewing conditions. When color video displays are used in time-critical applications (e.g., head-up displays, video control panels), the observer must discriminate among briefly presented targets seen within a complex spatial scene. We compare color-discrimination thresholds by using two tasks. In one task the observer makes color matches between two halves of a continuously displayed bipartite field. In a second task the observer detects a color target in a set of briefly presented objects. The data from both tasks are well summarized by ellipsoidal isosensitivity contours. The fitted ellipsoids differ both in their size, which indicates an absolute sensitivity difference, and orientation, which indicates a relative sensitivity difference.

Calibration↗

PubMed1990

Surface characterizations of color thresholds.

We evaluate how well three different parametric shapes, ellipsoids, rectangles, and parallelograms, serve as models of three-dimensional detection contours. We describe how the procedures for deriving the best-fitting shapes constrain inferences about the theoretical visual detection mechanisms. The ellipsoidal shape, commonly assumed by vector-length theories, is related to a class of visual mechanisms that are unique only up to orthogonal transformations. The rectangle shape is related to a unique set of visual mechanisms, but since the rectangle is not invariant with respect to linear transformations the estimated visual mechanisms are dependent on the stimulus coordinate frame. The parallelogram is related to a unique set of visual mechanisms and can be derived by methods that are independent of the stimulus coordinate frame. We evaluate how well these shapes approximate detection contours, using 2-deg test fields with a long (1-sec) Gaussian time course. Two statistical tests suggest that the parallelogram model is too strong. First, we find that the ellipsoid and rectangle shapes fit the data with the same precision as the variance in repeated threshold measurements. The parallelogram model, which has more free parameters, fits the data with more precision than the variance in repeated threshold measurements. Second, although the parallelogram model provides a slightly better fit of our data than the other two shapes, it does not serve as a better guide than the ellipsoidal model for interpolating from the measurements to thresholds in novel color directions.

Calibration↗