An Experimental Study on the Luminance Perception of Lighting Environment

Considering the characteristics of vision in the low luminance and weak contrast environment, this research obtains a series of simulant scenes. By means of experiment observation, quantification analysis and subjective evaluation, this research proposes a kind of scientific and controllable methods and modes, then relates the quantitative index and the qualitative description in order to take physics and psychological factor into the comprehensive consideration in lighting environment. Finally, it obtains the scope of luminance stimulus and the quantification relations. The results of this research can provide theoretical basis, model and quantitative suggests for corresponding standards. It has significance to urban lighting planning, design and management.

Primate Pupillary Light Reflex: Receptive Field Characteristics of Pretectal Luminance Neurons

This study examined the response properties of luminance neurons found within the pretectal olivary nucleus (PON), which is the pretectal nucleus that mediates the primate pupillary light reflex. We recorded the activity of 121 single units in alert, behaving rhesus monkeys trained to fixate a back-projected laser spot while a luminance stimulus was presented. The change in the firing rate of luminance neurons was measured as a function of changes in the size, retinal illuminance, and position of the stimulus. We found that these neurons possessed large receptive fields, which were sufficiently distinct that they could be placed into three classes. Approximately 40% of the PON luminance neurons responded well to stimuli presented in either the contralateral or ipsilateral hemifield. These neurons were classified as “bilateral” neurons. In the primate, retinal projections to the pretectum and other retinorecipient nuclei are organized such that direct retinal input can only account for the contralateral hemifield responses of these neurons. Thus the representation of the ipsilateral hemifield in “bilateral” PON cells must result from input from a nonretinal source. Approximately 30% of PON neurons responded only to stimuli presented in the contralateral hemifield. These neurons were classified as “contralateral” neurons. Finally, approximately 30% of PON neurons responded to stimuli presented at or near the animal's fixation point. These neurons were classified as “macular” neurons. The mean firing rates of all classes of neurons increased with increases in stimulus size and luminance within their receptive fields. The thresholds and magnitude of these responses closely matched those that would be appropriate for mediating the pupillary light reflex. In summary, these results suggest that all three classes of PON neurons contribute to the behaviorally observed pupillomotor field characteristics in which stimuli at the macular produce substantially larger pupillary responses than more peripheral stimuli. The contributions of “bilateral” and “contralateral” cells account for pupillary responses evoked by peripheral changes in luminance, whereas the contributions of all three cell classes account for the larger pupillary responses evoked by stimuli in the central visual field.

The uses of colour vision: behavioural and physiological distinctiveness of colour stimuli

Colour and greyscale (black and white) pictures look different to us, but it is not clear whether the difference in appearance is a consequence of the way our visual system uses colour signals or a by–product of our experience. In principle, colour images are qualitatively different from greyscale images because they make it possible to use different processing strategies. Colour signals provide important cues for segmenting the image into areas that represent different objects and for linking together areas that represent the same object. If this property of colour signals is exploited in visual processing we would expect colour stimuli to look different, as a class, from greyscale stimuli. We would also expect that adding colour signals to greyscale signals should change the way that those signals are processed. We have investigated these questions in behavioural and in physiological experiments. We find that male marmosets (all of which are dichromats) rapidly learn to distinguish between colour and greyscale copies of the same images. The discrimination transfers to new image pairs, to new colours and to image pairs in which the colour and greyscale images are spatially different. We find that, in a proportion of neurons recorded in the marmoset visual cortex, colour–shifts in opposite directions produce similar enhancements of the response to a luminance stimulus. We conclude that colour is, both behaviourally and physiologically, a distinctive property of images.

Achromatic Transparency and the Role of Local Contours

In this paper we investigate the role of contours and junctions in the perception of single-plane achromatic transparency. In order to measure the accuracy with which observers encode transparency, a six-luminance stimulus was employed in which the figural properties could be easily manipulated. Accuracy was measured by requiring subjects to select (either by the method of adjustment or by using a forced-choice procedure) the luminance that best completed a simulated transparent filter. The X junctions in the stimulus were destroyed or perturbed in three experiments. Simple occlusion of the junction (experiment 1), and perturbation of the orientation of the contours of the filter as they pass through the junction (experiment 3) resulted in small but significant reductions in performance. On the other hand, a sudden change in orientation of the background (material) contours (experiment 2) resulted in a small but significant enhancement of overall performance compared with the control stimulus. In the forced-choice task, reversals in the polarity of contours (as defined by the brightness order of flanking regions) around the junction were shown to effect large changes in subjects' accuracy in processing transparency. The overall results show that X and Ψ junctions are indeed salient properties of transparent stimuli. The findings suggest that jagged contours with sudden changes in direction are more likely to be attributed to reflectance (material) changes than to changes due to a transparent filter (or to illumination).

Color Processing in Macaque Striate Cortex: Relationships to Ocular Dominance, Cytochrome Oxidase, and Orientation

We located clusters of color-selective neurons in macaque striate cortex, as mapped with optical imaging and confirmed with electrophysiological recordings. By comparing responses to an equiluminant red/green stimulus versus a high-contrast luminance stimulus, we were able to reveal a patchy distribution of color selectivity. Other color imaging protocols, when compared with electrophysiological data, did not reliably indicate the location of functional structures. The imaged color patches were compared with other known functional subdivisions of striate cortex. There was a high degree of overlap of the color patches with the cytochrome-oxidase (CO) blobs. The patches were often larger than a single blob in size, however, and in some instances spanned two neighboring blobs. More than one-half (56%) of the color-selective patches seen in optical imaging were not confined to one ocular dominance (OD) column. Almost one-quarter of color patches (23%) extended across OD columns to encompass two blobs of different eye preference. We also compared optical images of orientation selectivity to maps of color selectivity. Results indicate that the layout of orientation and color selectivity are not directly related. Specifically, despite having similar scales and distributions, the maps of orientation and color selectivity were not in consistent alignment or registration. Further, we find that the maps of color selectivity and of orientation are each only loosely related to maps of OD. This description stands in contrast to a common depiction of color-selective regions as identical to CO blobs, appearing as pegs in the centers of OD columns in the classical “ice cube” model. These results concerning the pattern of color selectivity in V1 support the view (put forth in previous imaging studies of the organization of orientation and ocular dominance) that there is not a fundamental registration of functional hypercolumns in V1.

Foveal Attention Modulates Responses to Peripheral Stimuli

When attending to a visual object, peripheral stimuli must be monitored for appropriate redirection of attention and gaze. Earlier work has revealed precentral and posterior parietal activation when attention has been directed to peripheral vision. We wanted to find out whether similar cortical areas are active when stimuli are presented in nonattended regions of the visual field. The timing and distribution of neuromagnetic responses to a peripheral luminance stimulus were studied in human subjects with and without attention to fixation. Cortical current distribution was analyzed with a minimum L1-norm estimate. Attention enhanced responses 100–160 ms after the stimulus onset in the right precentral cortex, close to the known location of the right frontal eye field. In subjects whose right precentral region was not distinctly active before 160 ms, focused attention commonly enhanced right inferior parietal responses between 180 and 240 ms, whereas in the subjects with clear earlier precentral response no parietal enhancement was detected. In control studies both attended and nonattended stimuli in the peripheral visual field evoked the right precentral response, whereas during auditory attention the visual stimuli failed to evoke such response. These results show that during focused visual attention the right precentral cortex is sensitive to stimuli in all parts of the visual field. A rapid response suggests bypassing of elaborate analysis of stimulus features, possibly to encode target location for a saccade or redirection of attention. In addition, load for frontal and parietal nodi of the attentional network seem to vary between individuals.

Speed Discrimination in Luminance and Colour Stimuli as a Function of Contrast

We measured speed discrimination for isoluminant red - green and luminance-defined moving stimuli. The horizontal profile of the stimuli was a Gabor function with a carrier frequency of 2 cycles deg−1. The standard stimulus was a luminance stimulus with a fixed speed of 2 deg s−1 and a fixed contrast of 0.1. The comparison stimuli were either luminance stimuli (cone contrasts: 0.05, 0.1, 0.2, 0.4) or chromatic stimuli (cone contrasts: 0.025, 0.05, 0.1). The speed of the comparison stimuli was varied by an adaptive procedure. After each trial the observer indicated which of the 2 intervals contained the slower moving stimulus. The stimuli always moved horizontally and the direction was chosen randomly at each trial. The main findings were: (i) For luminance stimuli, the perceived speed was independent of contrast (ranging from 0.1 to 0.4). For colour stimuli, the perceived speed increased with contrast for two out of four observers. (ii) The sensitivity for speed discrimination was independent of contrast for luminance and for colour stimuli. (iii) There was no consistent difference in speed discrimination sensitivity between colour and luminance stimuli when the stimuli were equated in cone contrast.

Autokinesis of an Intermittent Luminance

20 Ss were used in an experiment to determine whether autokinetic latency and displacement of an intermittent luminance reach minimum and maximum, respectively, at the same rate of intermittence. It was found that autokinetic latency and displacement of a small, low-luminance stimulus reach minimum and maximum, respectively, in the region of 2 to 16 cps. Measures repeated over 5 days disclosed no systematic effects of repeated exposures to the illusion.