Biomedical subjects

Kathy T Mullen

Publications and source records attributed to Kathy T Mullen.

14 recordsLinked to original sources

PubMed2006

Cone weights for the two cone-opponent systems in peripheral vision and asymmetries of cone contrast sensitivity.

In understanding the basis of the changes in human color vision across eccentricity, one key piece of information remains unknown, whether the relative cone weights of the two cone opponent mechanisms vary. Here we measure detection threshold contours within three planes in a 3-dimensional cone contrast space to reveal the L, M and S-cone weights to the two cone opponent mechanisms, L/M and S/(L+M). We find these remain constant across eccentricity suggesting the underlying structures of the cone opponent mechanisms are invariant. The contrast sensitivities of two poles of the S-cone opponent mechanism also remain symmetrical, whereas small asymmetries develop in L/M opponency from about 15 degrees.

Color Perception↗

PubMed2006

Absence of S-cone input in human blindsight following hemispherectomy.

Destruction of the occipital cortex presumably leads to permanent blindness in the contralateral visual field. Residual abilities to respond to visual stimuli in the blind field without consciously experiencing them have, however, been described in cortically blind patients and are termed 'blindsight'. Although the neuronal basis of blindsight remains unknown, possible neuronal correlates have been proposed based on the nature of the residual vision observed. The most prominent but still controversial hypothesis postulates the involvement of the superior colliculi in blindsight. Here we demonstrate, using a computer-based reaction time test in a group of hemispherectomized subjects, that human 'attention-blindsight' can be measured for achromatic stimuli but disappears for stimuli that solely activate S-cones. Given that primate data have shown that the superior colliculi lacks input from S-cones, our results lend strong support to the hypothesis that 'attention-blindsight' is mediated through a collicular pathway. The contribution of a direct geniculo-extrastriate-koniocellular projection was ruled out by testing hemispherectomized subjects in whom a whole hemisphere has been removed or disconnected for the treatment of epilepsy. A direct retino-pulvinar-cortical connection is also unlikely as the pulvinar nucleus is known to receive input from S-cones as well as from L/M-cone-driven colour-opponent ganglion cells.

Adult↗

PubMed2005

Orientation discrimination in human vision: psychophysics and modeling.

We evaluated orientation discrimination thresholds using an external noise paradigm. Stimuli were spatiotemporal Gaussian patches of 2D orientation noise band-pass filtered in Fourier domain. Orientation acuity was measured for various combinations of stimulus spatial bandwidth, spatial frequency, and size as a function of orientation bandwidths of the stimuli. Stimulus contrast was matched in multiples of detection threshold. Consistent with the idea that stimulus orientation bandwidth acts as a source of external noise, orientation discrimination thresholds increased monotonically in all conditions with stimulus bandwidth. To interpret these results quantitatively, we first fitted a variance summation model to the data and derived the internal orientation noise, relative sampling efficiency, and orientation tuning of the mechanism underlying orientation discrimination. Due to the equivocal biological nature of these parameters for orientation discrimination, we investigated, with a modeling approach, how neural detectors characterized by a broad orientation tuning may support orientation discrimination. We demonstrated using the ideal-observer theory that while linear models, based on either unimodal filtering or center-surround opponency, predict the monotonic relationship between orientation discrimination threshold and orientation noise, a nonlinear model incorporating a broadband divisive inhibition in the orientation domain is a better candidate due to its contrast invariance. This model, using broad and similar orientation tuning for its excitatory and inhibitory inputs, accounts for the acute orientation acuity of human vision and proves to be robust despite the variance found in natural stimuli.

Discrimination, Psychological↗

PubMed2005

The role of perception, language, and preference in the developmental acquisition of basic color terms.

When learning basic color vocabulary, young children show a selective delay in the acquisition of brown and gray relative to other basic color terms. In this study, we first establish the robustness of this finding and then investigate the extent to which perception, language, and color preference may influence color conceptualization. Experimental tasks were designed to measure different aspects of perceptual color processing (discrimination and saliency), color preference and objective counts of color term frequency in preschool-directed language (books and mothers' speech) were used to compare the acquisition of three groups of colors: primary colors, secondary colors (orange, pink, and purple) that appear at the same time as the primary colors, and secondary colors (brown and gray) that appear late. Although our results suggest that perception does not directly shape young children's color term acquisition, we found that children prefer brown and gray significantly less than basic colors and that these color terms appear significantly less often in child-directed speech, suggesting that color preference, linguistic input, and developing color cognition may be linked.

Child Development↗

PubMed2005

Orientation selectivity in luminance and color vision assessed using 2-d band-pass filtered spatial noise.

We evaluated orientation discrimination in color and luminance vision using an external noise paradigm. Stimuli were spatiotemporal patches of 2D orientation noise isolating the achromatic, red-green and blue-yellow mechanisms, and matched in multiples of contrast detection threshold. We found a monotonic increase of orientation discrimination thresholds with the stimuli orientation bandwidths that is similar for both color and luminance contrasts. This dependence was fitted with two suitable models. A variance summation model suggests that internal orientation noise is significantly greater for the chromatic than for the achromatic mechanisms, while the efficiencies are similar. A gain control model of orientation tuning suggests that both chromatic and achromatic mechanisms are characterized by broadly tuned orientation detectors and that the relative chromatic deficit in orientation discrimination may only result from a slightly broader orientation tuning for the chromatic mechanisms. The moderate deficiency in chromatic orientation discrimination may account for the small differences found in shape perception between color and luminance vision.

Color Perception↗

PubMed2005

Does L/M cone opponency disappear in human periphery?

We have assessed the optimal cone contrast sensitivity across eccentricity in human vision of the two cone-opponent mechanisms [L/M or red-green, and S/(L + M) or blue-yellow] and the luminance mechanism. We have used a novel stimulus, termed a 'sinring', that is a radially modulated sine-wave arc, Gaussian enveloped in both angular and radial directions. This stimulus overcomes the problem inherent in Gabor stimuli of confounding stimulus spatial frequency, size, and eccentricity and so allows contrast sensitivity to be tracked accurately into the periphery. Our results show that L/M cone opponency declines steeply across the human periphery and becomes behaviourally absent by 25-30 deg (in the nasal field). This result suggests that any L/M cone-opponent neurons found in primate peripheral retina beyond this limit are unlikely to be significant for colour contrast detection measured behaviourally.

Color Perception↗

PubMed2004

Differential impact of the FMR1 gene on visual processing in fragile X syndrome.

Fragile X syndrome (FXS) is the most common form of heritable mental retardation, affecting approximately 1 in 4000 males. The syndrome arises from expansion of a trinucleotide repeat in the 5'-untranslated region of the fragile X mental retardation 1 (FMR1) gene, leading to methylation of the promoter sequence and lack of the fragile X mental retardation protein (FMRP). Affected individuals display a unique neurobehavioural phenotype that includes striking visual-motor deficits. Here we provide neurobiological and behavioural evidence that supports the hypothesis that these visual-motor deficits are attributable to a magnocellular (M) visual pathway impairment. Immunohistochemical staining of a lateral geniculate nucleus (LGN) of a normal human male revealed high FMRP basal expression selectively within the M layers, suggesting an increased susceptibility of these neurons to the lack of FMRP as occurs in FXS. Similar staining of monkey LGNs for quantification purposes revealed that the difference is not an artefact of cell size differences between M and parvocellular (P) neurons. Further, Nissl staining of the LGNs of a male FXS patient revealed alaminar nuclei comprised of a homogenous population of small sized neurons, providing anatomical and morphological support for the idea that an M pathway pathology exists in FXS. Consistent with these neurobiological data, we have found that male patients with FXS have reduced sensitivity for psychophysical stimuli that probe the M pathway but not for those that probe the P pathway, a complementary visual stream that performs a separate set of early visual operations. Finally, male patients with FXS performed poorly on a global motion task but not on a form perception task, suggesting that the M pathway thalamic deficit may have a selective impact on cortical visual functioning in the parietal lobe, which is known to be a major recipient of M pathway afferents via the primary visual cortex. Together, these findings provide the first evidence that the loss of a single gene product, FMRP, in humans leads to abnormal neuroanatomical morphology of the LGN and a concomitant selective visual deficit of the M pathway.

Adolescent↗

PubMed2003

Failure of signed chromatic apparent motion with luminance masking.

It has been suggested that there are two types of chromatic motion mechanisms: signed chromatic motion, in which correspondence across successive frames is based on chromatic content of image regions, and unsigned chromatic motion based on movement of chromatically-defined borders. We investigate whether signed and unsigned red-green chromatic motion are mediated by a genuinely chromatic mechanism. Direction discrimination of signed and unsigned red-green chromatic motion were measured in the presence of a dynamic luminance masking noise. Increasing the luminance noise contrast systematically impaired signed motion, regardless of contrast and speed. This result suggests that signed red-green chromatic motion is derived from a luminance-based signal, rather than a genuinely chromatic motion mechanism. In the case of unsigned chromatic motion, there is no effect of luminance masking noise, indicating there exists a genuine chromatic mechanism for second-order motion perception.

Color Perception↗

PubMed2003

Luminance mechanisms mediate the motion of red-green isoluminant gratings: the role of "temporal chromatic aberration".

In this paper we use a dynamic noise-masking paradigm to explore the nature of the mechanisms mediating the motion perception of drifting isoluminant red-green gratings. We compare contrast thresholds for the detection and direction discrimination of drifting gratings (1.5 cpd), over a range of temporal frequencies (0.5-9 Hz) in the presence of variable luminance or chromatic noise. In the first experiment, we used dynamic luminance noise to show that direction thresholds for red-green grating motion are masked by luminance noise over the entire temporal range tested, whereas detection thresholds are unaffected. This result indicates that the motion of nominally isoluminant red-green gratings is mediated by luminance signals. We suggest that stimulus-based luminance artifacts are not responsible for this effect because there is no masking of the detection thresholds. Instead we propose that chromatic motion thresholds for red-green isoluminant gratings are mediated by dynamic luminance artifacts that have an internal, physiological origin. We have termed these "temporal chromatic aberration". In the second experiment, we used dynamic chromatic noise masking to test for a chromatic contribution to red-green grating motion. We were unable to find conclusive evidence for a contribution of chromatic mechanisms to the chromatic grating motion, although a contribution at very high chromatic contrasts cannot be ruled out. Our results add to a growing body of evidence indicating the presence of dynamic, internal luminance artifacts in the motion of chromatic stimuli and we show that these occur even at very low temporal rates. Our results are compatible with our previous work indicating the absence of a chromatic mechanism for first order (quasi-linear) apparent motion [Vision Res. 40 (2000) 1993]. We conclude that previous conclusions based on the motion of chromatic red-green gratings should be reassessed to determine the contribution of dynamic luminance artifacts.

Color Perception↗

PubMed2002

Comparison of color and luminance vision on a global shape discrimination task.

We compared the performances of the blue-yellow, red-green and luminance systems on a shape discrimination task. Stimuli were radial frequency patterns (radially modulated fourth derivative of a Gaussian) with a peak spatial frequency of 0.75 cpd. Stimuli isolated the chromatic (red-green and blue-yellow) and achromatic post-receptoral mechanisms. We showed that in all cases performance, measured as a radial modulation threshold for discrimination between a circular and non-circular stimulus, improves with contrast. Performance was compared across radial frequencies with contrast matched in multiples of stimulus detection threshold. We find that blue-yellow color system performs the worse on this shape discrimination task, followed by the red-green, with the achromatic system performing best. The average difference is a factor of 2 between achromatic and blue-yellow performance, and a factor of 1.7 between red-green and achromatic. Despite these performance losses, chromatic shape discrimination can still reach hyperacuity performance levels. In a secondary experiment we contrast modulate the radial contour to eliminate either the "corners" or "sides" of an RF4 (square) pattern. We find that for the achromatic system, the sides are more important for the task than the corners. However, for the chromatic system, removal of sides or corners produces similar performance deficits. We conclude that color vision has a selective although relatively mild deficit for two-dimensional form perception.

Color Perception↗

PubMed2002

Is the acquisition of basic-colour terms in young children constrained?

We investigated whether the learning of colour terms in childhood is constrained by a developmental order of acquisition as predicted by Berlin and Kay [1969 Basic Color Terms (Berkeley, CA: University of California Press)]. Forty-three children, aged between 2 and 5 years and grouped according to language ability, were given two tasks testing colour conceptualisation. Colour comprehension was assessed in a spoken-word-to-colour-matching task in which a target colour was presented in conjunction with two distractor colours. Colour naming was measured in an explicit naming task in which colours were presented individually for oral naming. Results showed that children's knowledge of basic-colour terms varied across tasks and language age, providing little support for a systematic developmental order. In addition, we found only limited support for an advantage for the conceptualisation of primary (red, green, blue, yellow, black, white) compared to non-primary colour terms across tasks and language age. Instead, our data suggest that children acquire reliable knowledge of nine basic colours within a 3-month period (35.6 to 39.5 months) after which there is a considerable lag of up to 9 months before accurate knowledge of the final two colours (brown and grey) is acquired. We propose that children acquire colour term knowledge in two distinct time frames that reflect the establishment of, first, the exterior (yellow, blue, black, green, white, pink, orange, red, and purple) and, second, the interior structure (brown and grey) of conceptual colour space. These results fail to provide significant support for the order predicted by Berlin and Kay, and suggest, instead, that the development of colour term knowledge is largely unconstrained.

Aging↗

PubMed2002

Ratio model serves suprathreshold color--luminance discrimination.

We extended earlier results [J. Opt. Soc. Am. A 16, 2625 (1999)] to examine how the responses of the three postreceptoral mechanisms are combined to subserve discrimination of suprathreshold stimuli. Test thresholds were obtained in the presence of suprathreshold pedestals selected in different quadrants of the red-green/luminance and blue-yellow/luminance planes of cardinal color space. We showed that (1) test threshold was directly proportional to pedestal contrast for pedestal contrasts exceeding five times pedestal contrast threshold, and (2) there were exceptions to this proportionality, notably when the test and pedestal directions were fixed in the cardinal directions. Results support a ratio model of suprathreshold color-luminance discrimination, in which discrimination depends on a ratio of outputs of the postreceptoral mechanisms. We also observed that when test threshold was measured as a function of test color-space direction, masking by the achromatic component of the pedestal was less than that by the chromatic component. In addition, masking by a dark (negative luminance component) pedestal was lower than masking by a light (positive luminance) pedestal of a similar contrast. Our results demonstrated that (1) there is no fundamental difference between discrimination in the isoluminant and in the two chromoluminant cardinal planes, (2) there exists the possibility that discrimination in cardinal directions differs from that in noncardinal (intermediate) directions, and (3) suprathreshold discrimination of luminance differences may be more sensitive than that of chromatic differences for a given suprathreshold pedestal.

Adult↗

PubMedDate not supplied

Differential distributions of red-green and blue-yellow cone opponency across the visual field.

The color vision of Old World primates and humans uses two cone-opponent systems; one differences the outputs of L and M cones forming a red-green (RG) system, and the other differences S cones with a combination of L and M cones forming a blue-yellow (BY) system. In this paper, we show that in human vision these two systems have a differential distribution across the visual field. Cone contrast sensitivities for sine-wave grating stimuli (smoothly enveloped in space and time) were measured for the two color systems (RG & BY) and the achromatic (Ach) system at a range of eccentricities in the nasal field (0-25 deg). We spatially scaled our stimuli independently for each system (RG, BY, & Ach) in order to activate that system optimally at each eccentricity. This controlled for any differential variations in spatial scale with eccentricity and provided a comparison between the three systems under equivalent conditions. We find that while red-green cone opponency has a steep decline away from the fovea, the loss in blue-yellow cone opponency is more gradual, showing a similar loss to that found for achromatic vision. Thus only red-green opponency, and not blue-yellow opponency, can be considered a foveal specialization of primate vision with an overrepresentation at the fovea. In addition, statistical calculations of the level of chance cone opponency in the two systems indicate that selective S cone connections to postreceptoral neurons are essential to maintain peripheral blue-yellow sensitivity in human vision. In the red-green system, an assumption of cone selectivity is not required to account for losses in peripheral sensitivity. Overall, these results provide behavioral evidence for functionally distinct neuro-architectural origins of the two color systems in human vision, supporting recent physiological results in primates.

Color Perception↗

PubMedDate not supplied

How long range is contour integration in human color vision?

We quantified and compared the effect of element spacing on contour integration between the achromatic (Ach), red-green (RG), and blue-yellow (BY) mechanisms. The task requires the linking of orientation across space to detect a contour in a stimulus composed of randomly oriented Gabor elements (1.5 cpd, sigma = 0.17 deg), measured using a temporal 2AFC method. A contour of ten elements was pasted into a 10 x 10 cells array, a ndbackground elements were randomly positioned within the available cells. The effect of element spacing was investigated by varying the mean interelement distance between two and six times the period of the Gabor elements (lambda = 0.66 deg) while the total number of elements was fixed. Contour detection was measured as a function of its curvature for jagged contours and for closed contours. At all curvatures, we found that performance for chromatic mechanisms declines more steeply with the increase in element separation than does performance for the achromatic mechanism. Averaged critical element separations were 4.6 +/- 0.7, 3.6 +/- 0.4, and 2.9 +/- 0.2 deg for Ach, BY, and RG mechanisms, respectively. These results suggest that contour integration by the chromatic mechanisms relies more on short-range interactions in comparison to the achromatic mechanism. In a further experiment, we looked at the combined effect of element size and element separation in contour integration for the Ach mechanism. We found that the critical separation decreases linearly with the spatial frequency, from about 5 deg at low spatial frequency (larger elements) to about 1 deg at high spatial frequency (smaller elements) suggesting a scale invariance in contour integration. In both experiments we also found no differences between closed and open jagged contours detection in terms of element separation. The neuroanatomical implications of these findings relatively to area V1 are discussed.

Color Perception↗