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K T Mullen

Publications and source records attributed to K T Mullen.

At least 19 recordsLinked to original sources
PubMed2001

Conceptualization of perceptual attributes: a special case for color?

Young children experience difficulties establishing conceptual representations of color compared with everyday objects. We argue that comparing the development of color cognition to that of familiar objects is inappropriate since color is a perceptual attribute that can be abstracted from an object and by itself lacks functional significance. Instead, we compared the recognition, perceptual saliency, and naming of color to that of three other perceptual object attributes (motion, form, and size) in 47 children aged 2 to 5 years as a function of language age. Results revealed that, although color was perceptually salient relative to the other visual attributes, no selective impairment to color cognition (recognition and naming) was found relative to the three other visual attributes tested. Thus, when the appropriate comparisons are made, we find no special delay in the development of color conceptualization. Furthermore, the striking disparity between perceptual saliency and cognition of color in our youngest age groups suggests that perceptual saliency has little influence on the conceptual development of color.

Child↗
PubMed2001

Dynamics of contour integration.

To determine the dynamics of contour integration the temporal properties of the individual contour elements were varied as well as those of the contour they form. A temporal version of a contour integration paradigm (Field, D. J., Hayes, A., & Hess, R. F. (1993) Vision Research, 33, 173-193) was used to assess these two temporal dynamics as a function of the contrast of individual elements and the curvature of the contour. The results show that the dynamics of contour integration are good when the contrast of the individual elements is modulated in time (10-30 Hz), but are poor when contour linking per se is temporally modulated (1-12 Hz). The dynamics of contour linking is not dependent on the absolute contrast of the linking elements, so long as they are visible, but does vary with the curvature of the contour. For straight contours, temporal resolution is around 6-12 Hz but falls to around 1-2 Hz for curved contours.

Analysis of Variance↗
PubMed2001

Processing time of contour integration: the role of colour, contrast, and curvature.

We investigated the temporal properties of the red - green, blue-yellow, and luminance mechanisms in a contour-integration task which required the linking of orientation across space to detect a 'path'. Reaction times were obtained for simple detection of the stimulus regardless of the presence of a path, and for path detection measured by a yes/no procedure with path and no-path stimuli randomly presented. Additional processing times for contour integration were calculated as the difference between reaction times for simple stimulus detection and path detection, and were measured as a function of stimulus contrast for straight and curved paths. We found that processing time shows effects not apparent in choice reaction-time measurements. (i) Processing time for curved paths is longer than for straight paths. (ii) For straight paths, the achromatic mechanism is faster than the two chromatic ones, with no difference between the red-green and blue-yellow mechanisms. For curved paths there is no difference in processing time between mechanisms. (iii) The extra processing time required to detect curved compared to straight paths is longest for the achromatic mechanism, and similar for the red - green and blue-yellow mechanisms. (iv) Detection of the absence of a path requires at least 50 ms of additional time independently of chromaticity, contrast, and path curvature. The significance of these differences and similarities between postreceptoral mechanisms is discussed.

Analysis of Variance↗
PubMed2000

Absence of a chromatic linear motion mechanism in human vision.

We have investigated motion mechanisms in central and perifoveal vision using two-frame random Gabor kinematograms with isoluminant red-green or luminance stimuli. In keeping with previous results, we find that performance dominated by a linear motion mechanism is obtained using high densities of micropatterns and small temporal intervals between frames, while nonlinear performance is found with low densities and longer temporal intervals [Boulton, J. C., & Baker, C. L. (1994) Proceedings of SPIE, computational vision based on neurobiology, 2054, 124-133]. We compare direction discrimination and detection thresholds in the presence of variable luminance and chromatic noise. Our results show that the linear motion response obtained from chromatic stimuli is selectively masked by luminance noise; the effect is selective for motion since luminance noise masks direction discrimination thresholds but not stimulus detection. Furthermore, we find that chromatic noise has the reverse effect to luminance noise: detection thresholds for the linear chromatic stimulus are masked by chromatic noise but direction discrimination is relatively unaffected. We thus reveal a linear 'chromatic' mechanism that is susceptible to luminance noise but relatively unaffected by color noise. The nonlinear chromatic mechanism behaves differently since both detection and direction discrimination are unaffected by luminance noise but masked by chromatic noise. The double dissociation between the effects of chromatic and luminance noise on linear and nonlinear motion mechanisms is not based on stimulus speed or differences in the temporal presentations of the stimuli. We conclude that: (1) 'chromatic' linear motion is solely based on a luminance signal, probably arising from cone-based temporal phase shifts; (2) the nonlinear chromatic motion mechanism is purely chromatic; and (3) we find the same results for both perifoveal and foveal presentations.

Color Perception↗
PubMed2000

Contour integration in color vision: a common process for the blue-yellow, red-green and luminance mechanisms?

We compare the performance of the red-green, blue-yellow and luminance postreceptoral mechanisms on a contour integration task requiring the linking of oriented Gabor elements across space to extract a winding 'path' or contour. We first establish that for all three mechanisms curvature and contrast are independent; losses in performance due to one cannot be compensated by changes in the other. We then compare contour integration by the three mechanisms using a method that controls for their differences in cone contrast thresholds. Our results show that despite the poor orientation discrimination thresholds and poor spatial sampling found for the blue-yellow mechanism, all three mechanisms perform similarly on contour integration over a wide range of curvatures. Furthermore, all three mechanisms have the same dependence on path curvature. We also investigate the effects of adding external orientation noise. Our results imply that the internal orientation noise for extracting 'aligned' path elements is similar in the three mechanisms and for all path curvatures, and the relative efficiencies are also similar for the three mechanisms. To account for our results, we propose that the three postreceptoral mechanisms use a common contour integration process. This linking process, however, cannot be color-blind; our last experiment shows that linking between different chromatic mechanisms or between opposite spatial phases disrupts contour integration. We thus propose that the common integration process remains sensitive to the color contrast and phase of its inputs.

Color Perception↗
PubMed2000

Role of chromaticity, contrast, and local orientation cues in the perception of density.

We compared the role of the red-green, blue-yellow, and luminance post-receptoral mechanisms in the perception of density. The task requires the comparison of densities between two stimuli composed of oriented bandpass elements, pseudo-randomly scattered across an area of constant size. The perception of density differences was measured by a temporal 2AFC procedure for all pairs of mechanisms and for four possible densities. We found that stimuli of identical physical densities are not perceived equally: there is a consistent bias in favour of blue-yellow stimuli which are perceived as significantly more dense than red-green and achromatic stimuli. We considered three factors that could have differentially affected the density perception of blue-yellow stimuli: an increase in the perceived size of the individual blue-yellow elements, a perceived contrast difference, and the presence of local orientation cues. We found that the increased perceived density of the blue-yellow stimuli occurred despite the fact that there was no increase in perceived size of the individual elements, and remained despite corrections for the two other factors. We conclude that the significant increase in perceived density for the blue-yellow mechanism is a global effect, associated with a perceived colour 'melting' of the elements in the array. Our data were fitted with the occupancy model of Allik and Tuulmets (1991, Perception & Psychophysics 49 303-314) and we found that blue-yellow stimuli have a greater 'occupancy' than red-green or achromatic stimuli.

Color Perception↗
PubMed2000

Evidence for mild blue-yellow colour vision deficits immediately following fluorescein angiography.

AIMS: We have investigated the short term effects of fluorescein angiography on the blue-yellow, red-green, and luminance contrast sensitivity of patients with early age-related macular degeneration (ARMD). METHODS: Nine ARMD patients with no exudative complications and a visual acuity of 20/60 or better in the tested eye were selected. Cardinal colour directions for the isolation of the red-green, blue-yellow and achromatic (luminance) visual mechanisms were determined for each patient. Contrast sensitivity was measured in each cardinal colour direction immediately before and 20 min after standard 20-flash fluorescein angiography. RESULTS: A significant, albeit mild, reduction for blue-yellow contrast sensitivity following angiography was observed (ANOVA, alpha = 0.05). Fluorescein angiographic exposure had no significant effect on red-green or luminance contrast sensitivity. CONCLUSION: Our results show that fluorescein angiography causes at least a short term deficit selective to blue-yellow contrast sensitivity in our patient group.

Aged↗
PubMed1999

Evidence for the stochastic independence of the blue-yellow, red-green and luminance detection mechanisms revealed by subthreshold summation.

We investigated the manner in which the outputs of the three postreceptoral mechanisms (red-green, blue-yellow and luminance) combine to determine contrast threshold. We used a subthreshold summation paradigm to test whether the combination of the postreceptoral mechanism outputs could be described by a probability summation model which assumes stochastic independence of the mechanisms, and determined the best fitting summation exponent. Stimuli were Gaussian enveloped 1 c/d sinusoidal gratings represented in a 3D cardinal space transformed from cone contrast axes, and normalized to detection threshold. The use of this space avoids the presence of elongated threshold contours, allowing a reliable model fit to include the less sensitive blue-yellow and luminance mechanisms. Our results were well fitted by the probability summation model and hence support the underlying stochastic independence of the three postreceptoral mechanisms.

Chi-Square Distribution↗
PubMed1999

The spatial tuning of color and luminance peripheral vision measured with notch filtered noise masking.

We have measured the spatial bandwidths of the bandpass red-green chromatic and luminance mechanisms at four locations in the nasal visual field (0, 10, 20 and 30 degrees) using a method of notch filtered noise masking which effectively removes the artifact of off-frequency looking for our stimuli. Detection thresholds were measured for luminance or isoluminant red-green Gaussian enveloped test gratings of 0.5 cpd embedded in 1/f noise. Firstly, thresholds were obtained as a function of increasing noise spectral density and were fitted using a standard noise masking model. These results support the existence across the visual field of independent, red-green chromatic and luminance mechanisms with similar sampling efficiencies. Secondly, we measured thresholds in notch filtered noise as a function of notch width and derived the spatial bandwidth of the detection mechanism. We find both color and luminance mechanisms have similar bandwidths which remain virtually constant across eccentricity. These results indicate strong overall similarities between the early processing of color and luminance vision, and lend support to the role of color as an 'intrinsic image' in spatial vision. The results are discussed in the light of the anchored channel and shifting channel models of peripheral contrast sensitivity and pattern detection.

Color Perception↗
PubMed1999

Ratio model for suprathreshold hue-increment detection.

We use psychophysical techniques to investigate the neural mechanisms subserving suprathreshold chromatic discrimination in human vision. We address two questions: (1) How are the postreceptoral detection mechanism responses combined to form suprathreshold chromatic discriminators? and (2) How do these discriminators contribute to color perception? We use a pedestal paradigm in which the subject is required to distinguish between a pedestal stimulus and the same pedestal added to a chromatic increment (the test). Our stimuli are represented in a cardinal space, in which the axes express the responses of the three postreceptoral detection mechanisms normalized relative to their respective detection thresholds. In the main experiment the test (a hue increment) was fixed in the direction orthogonal to the pedestal in our cardinal space. We found that, for high pedestal contrasts, the test threshold varied proportionally with the pedestal contrast. This result suggests the presence of a hue-increment detector dependent on the ratio of the outputs from the red-green and blue-yellow postreceptoral detection mechanisms. The exception to this was for pedestals and tests fixed along the cardinal axes. In that case detection was enhanced by direct input from the postreceptoral mechanism capable of detecting the test in isolation. Our results also indicate that discrimination in the red-green/luminance and blue-yellow/luminance planes exhibits a behavior similar to discrimination within the isoluminant plane. In the final experiment we observed that thresholds for hue-increment identification (e.g., selecting the bluer of two stimuli) are also governed by a ratio relationship. This finding suggests that our ratio-based mechanisms play an important role in color-difference perception.

Adult↗
PubMed1998

A nonlinear chromatic motion mechanism.

Previous research has demonstrated two categorically distinct mechanisms mediating apparent motion of kinematograms composed of eccentricity-confined, randomly placed Gabor micropatterns: a quasi-linear mechanism operating for high micropattern densities and short time separations, and a nonlinear mechanism operating at low micropattern densities or longer time separations. Here we compare the performance of these two mechanisms using color (isoluminant) and luminance-defined stimuli. When these stimuli are defined only by their color contrast, the response of the quasi-linear mechanism is severely impaired, while the nonlinear mechanism remains fully operative. This result further strengthens the dichotomy between the two kinds of motion perception, and suggests that when color vision supports motion perception it does so primarily, or perhaps entirely, via a nonlinear mechanism.

Color Perception↗
PubMed1997

Absence of linear subthreshold summation between red-green and luminance mechanisms over a wide range of spatio-temporal conditions.

We have tested the independence of red-green chromatic and luminance mechanisms at detection threshold using a method of subthreshold summation. Stimuli were isoluminant red-green gratings and yellow-black luminance gratings that uniquely activate the red-green color and luminance mechanisms, respectively. Stimuli were Gaussian enveloped 0.25, 1 or 4 cpd sinewave gratings, counter-phase flickered at 0, 5 or 9 Hz. The threshold detection of red-green color contrast was measured in the presence of a subthreshold amount of luminance contrast, and vice versa. The results allow a model of linear summation between the color and luminance mechanisms to be rejected, but are well fitted by a model, assuming that these mechanisms are independent but combine to determine detection by probability summation, with a high summation index (median value = 4). We conclude that there are independent red-green chromatic mechanism and luminance detection mechanisms over this range of spatio-temporal conditions.

Color Perception↗
PubMed1997

Red-green and achromatic temporal filters: a ratio model predicts contrast-dependent speed perception.

We simultaneously measured detection and identification performance by using isoluminant red-green (RG) and achromatic flickering stimuli and fitted these data with a modified line-element model that does not make high-threshold assumptions. The modeling shows that detection and identification data are adequately described by postulating only two underlying temporal filters each for RG and achromatic vision, even when more than two threshold classifications are evident. We use a spatial frequency of 1.5 cycles per degree (c/deg) and compare the derived temporal impulse response functions with those obtained previously with the use of 0.25 c/deg stimuli under otherwise identical conditions [J. Opt. Soc. Am. A 13, 1969 (1996)]. We find that at 1.5 c/deg the luminance impulse response functions peak later and integrate out to longer times compared with those measured at 0.25 c/deg. For RG stimuli, although their relative overall sensitivities change, the impulse response functions are similar across spatial frequency, indicating a constancy of chromatic temporal properties across spatial scales. In a second experiment, we measured RG and achromatic flicker discrimination over a wide range of suprathreshold contrasts. These data suggest a common nonlinear contrast response function operating after initial temporal filtering. Using a ratio model of speed perception in which both RG and achromatic filters are combined at a common motion site, we can predict (1) the perceived slowing of RG stimuli compared with the perceived drift of achromatic drifting stimuli, (2) the contrast dependency of speed perception for RG and achromatic drifting stimuli, and (3) how this dependency changes with base speed. Thus we conclude that there is no need to postulate separate mechanisms for fast and slow motion [Nature (London) 367, 268 (1994)], since a unified ratio model can explain both RG and achromatic contrast-speed dependency.

Color Perception↗
PubMed1997

Postreceptoral chromatic detection mechanisms revealed by noise masking in three-dimensional cone contrast space.

We used a noise masking technique to test the hypothesis that detection is subserved by only two chromatic postreceptoral mechanisms (red-green and blue-yellow) and one achromatic (luminance) mechanism. The task was to detect a 1-c/deg Gaussian enveloped grating presented in a mask of static, spatially low-passed binary or Gaussian distributed noise. In the main experiment, the direction of the test stimulus (termed the signal) was constant in cone contrast space, and the direction of the noise was sampled in equally spaced directions within a plane (the noise plane) in the space. The signal was chosen to coincide with one of the three cardinal directions of three postulated mechanisms. The noise plane was selected to span two of the cardinal directions, including that chosen as the signal direction. As the noise direction was sampled around the noise plane, the signal detection threshold was found to vary in accordance with a linear cosine model, which predicted noise directions yielding maximum and minimum masking of the signal. In the direction of minimum masking (termed a null direction), the noise was found to have no masking effect on the signal. Moreover, the null was not orthogonal to the signal direction but lay instead in one of the cardinal directions. Our findings suggest that detection is mediated by only three mechanisms. In a further experiment we found little or no cross masking between each pair of cardinal directions up to the limit of our noise mask contrasts. This further supports the presence of no more than three independent postreceptoral mechanisms.

Artifacts↗
PubMed1996

Color and luminance vision in human amblyopia: shifts in isoluminance, contrast sensitivity losses, and positional deficits.

The deficits for contrast detection and positional accuracy were compared for chromatic and luminance mechanisms within a group of strabismic and anisometropic amblyopes. We found that the isoluminant point was shifted towards red in the amblyopic compared to the fellow normal eye. This was not accounted for by eccentric fixation by the amblyopic eye. Contrast sensitivity deficits were similar for luminance and color stimuli in normal and amblyopic visual systems. In the majority of our amblyopic subjects, however, the deficits in positional acuity were greater for the chromatic than the luminance stimuli.

Adolescent↗
PubMed1996

Contour integration with colour and luminance contrast.

In this study, we consider how colour contrast can be used to integrate form and how it interacts with luminance contrast in the task. The performance of form integration was assessed by measuring the detection of a winding "contour" of aligned gabor elements embedded in a background of randomly oriented gabors, using both luminance and isoluminant (red/green) contrast. Performance on the task improves with gabor element contrast, and identical performance for colour and luminance contour detection is achieved at high screen contrasts, showing that colour is able to support a complex form integration task. In a second experiment, we investigate whether colour and luminance contrast can be combined in contour integration by measuring the detection of a path with alternating isoluminant colour and luminance elements. We find that contour detection uses both colour and luminance information cooperatively, but performance is much poorer than would be expected from a single common contour integration process which fails to distinguish the two types of contrast. This suggests that there are specific contour integration processes for colour and luminance. In a third experiment, we measure the effects of variations in colour and luminance contrast on contour detection using elements that combine colour and luminance contrast. We find that varying the colour contrast of elements tends to worsen the detection of a luminance contour, as do luminance contrast variations for colour contour detection. These results suggest no special role for colour in integrating contours, and are discussed with regard to their ecological significance.

Algorithms↗
PubMed1996

Losses in peripheral colour sensitivity predicted from "hit and miss" post-receptoral cone connections.

On the basis of the early primate neurophysiological recordings, it was thought that the different cone types of the primate retina project selectively into the centre and surround of the receptive fields of cone opponent neurons, and more recently this view has been reasserted on the basis of physiological results. An alternative idea is that these projections are in fact unselective for cone type, and, therefore, cone opponency arises from chance variations in the proportions of different cone types in centre and surround. The issue is presently controversial with anatomical or physiological support for both hypotheses. Our results show that there is a selective loss of red-green colour sensitivity across the human visual field. Furthermore, this selective loss occurs under low temporal frequency conditions (0.5 Hz) which were selected to favour the mediation of both colour and luminance detection by a common P cell pathway and to exclude an M cell contribution to detection threshold. We show that "hit and miss" post-receptoral cone projections will produce a decline in cone opponency that is sufficient to account for this selective loss, thus providing psychophysical evidence consistent with this hypothesis.

Color Perception↗