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Previous studies identified two visual stimuli that can shorten the human eye by thickening the choroid after short-term visual stimulation, potentially inhibiting myopia: (1) watching digitally filtered movies where the red plane has full spatial resolution while green and blue are low-pass filtered according to the human longitudinal chromatic aberration (LCA) function (the "red in focus" filter), and (2) reading text with inverted contrast. This study aimed to determine whether combining these two stimuli would have an additive effect on axial length. Twenty-two emmetropic subjects were recruited to read text (standard and inverted contrast) for 30 min from a large screen, 2 m away, either unfiltered or filtered with the "red in focus" filter. Axial length was measured before and after each reading episode using low-coherence interferometry (Lenstar LS 900, Haag Streit). Reading text with conventional contrast polarity (dark letters on a bright background) resulted in no significant axial length change. Adding the "red in focus" filter did not alter the outcome. Consistent with previous findings, reading inverted contrast text made emmetropic eyes shorter. Surprisingly, when the text was combined with the "red in focus" filter, eyes became longer rather than shorter. A possible explanation for this contradictory result is that, for the text stimulus, the "red in focus" filter removes spatial information in the blue channel needed by the retina to use LCA analysis to thicken the choroid.

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New type desktop head-up display (HUD) can reduce visual fatigue and protect vision through long viewing distance. In this study, participants evaluated visual performance, fatigue, and discomfort of desktop HUD under two contrast polarity (N = 36) and five display luminance levels (N = 21). A positive polarity advantage was found over negative in visual fatigue and discomfort (p < .05). Statistically significant effect of luminance was found on visual performance, fatigue, and discomfort (p < .05). The calculated optimum display luminance by the proposed inverted-U fitted model was 153 cd/m2 under 300 lx, higher than that of traditional desktop displays. It is speculated that higher luminance is required to offset the reduction in contrast sensitivity due to smaller target angular size, which caused by longer viewing distance. These findings suggest that positive polarity and 153 cd/m2 can be used to improve performance and avoid fatigue and discomfort when utilising desktop HUD under 300 lx.

A visual ergonomic study was conducted on new type desktop HUD. With visual performance, fatigue, and discomfort as optimisation goals, positive polarity and 153 cd/m² was recommended under 300 lx. Compared with traditional desktop displays, higher luminance was required in desktop HUD under the same illumination.

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The ability to detect faces in the environment is of utmost ecological importance for human social adaptation. While face categorization is efficient, fast and robust to sensory degradation, it is massively impaired when the facial stimulus does not match the natural contrast statistics of this visual category, i.e., the typically experienced ordered alternation of relatively darker and lighter regions of the face. To clarify this phenomenon, we characterized the contribution of natural contrast statistics to face categorization. Specifically, 31 human adults viewed various natural images of nonface categories at a rate of 12 Hz, with highly variable images of faces occurring every eight stimuli (1.5 Hz). As in previous studies, neural responses at 1.5 Hz as measured with high-density electroencephalography (EEG) provided an objective neural index of face categorization. Here, when face images were shown in their naturally experienced contrast statistics, the 1.5-Hz face categorization response emerged over occipito-temporal electrodes at very low contrast [5.1%, or 0.009 root-mean-square (RMS) contrast], quickly reaching optimal amplitude at 22.6% of contrast (i.e., RMS contrast of 0.041). Despite contrast negation preserving an image's spectral and geometrical properties, negative contrast images required twice as much contrast to trigger a face categorization response, and three times as much to reach optimum. These observations characterize how the internally stored natural contrast statistics of the face category facilitate visual processing for the sake of fast and efficient face categorization.

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Metacontrast masking is a powerful illusion to investigate the dynamics of perceptual processing and to control conscious visual perception. However, the neural mechanisms underlying this fundamental investigative tool are still debated. In the present study, we examined metacontrast masking across different contrast polarities by employing a contour discrimination task combined with EEG (Electroencephalography). When the target and mask had the same contrast polarity, a typical U-shaped metacontrast function was observed. A change in mask polarity (i.e., opposite mask polarity) shifted this masking function to a monotonic increasing function such that the target visibility was strongly suppressed at stimulus onset asynchronies less than 50 ms. This transition in metacontrast function has been typically interpreted as an increase in intrachannel inhibition of the sustained activities functionally linked to object visibility and identity. Our EEG analyses revealed an early (160-300 ms) and a late (300-550 ms) spatiotemporal cluster associated with this effect of polarity. The early cluster was mainly over occipital and parieto-occipital scalp sites. On the other hand, the later modulations of the evoked activities were centered over parietal and centro-parietal sites. Since both of these clusters were beyond 160 ms, the EEG results point to late recurrent inhibitory mechanisms. Although the findings here do not directly preclude other proposed mechanisms for metacontrast, they highlight the involvement of recurrent intrachannel inhibition in metacontrast masking.

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The extent to which processing of abstract numerical concepts depends on perceptual representations is still an open question. In four experiments, we examined the association between contrast polarity and mental arithmetic, as well as its possible source. Undergraduate psychology students verified the correctness of single-digit arithmetic problems such as 2 + 5 = 7 or 9 - 6 = 5. Problems appeared either in white or black on a grey background, thus creating positive or negative contrast polarity, respectively. When the correct response was Yes (No), participants were faster (slower) in verifying positive than negative addition problems and in verifying negative than positive subtraction problems. Experiment 2 confirmed that the same result also held for written word problems (e.g., SEVEN + SIX = THIRTEEN). However, Experiment 3 found that the effect of contrast polarity observed in Experiments 1 and 2 disappeared in a blocked design where arithmetic operation was a between-participant factor. In addition, Experiment 4 revealed that the effect of contrast polarity does not generalise to multiplication and division. Overall, available evidence suggests that participants spontaneously associate the abstract relation between addition and subtraction (more-less) with a similar relation between contrast polarities (bright-dark).

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Pinna and Conti (Brain Sci., 2019, 9, 149, doi:10.3390/brainsci9060149) presented phenomena concerning the salience and role of contrast polarity in human visual perception, particularly in amodal completion. These phenomena are indeed illustrative thereof, but here, the focus is on their claims (1) that neither simplicity nor likelihood approaches can account for these phenomena; and (2) that simplicity and likelihood are equivalent. I argue that their first claim is based on incorrect assumptions, whereas their second claim is simply untrue.

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In this work, we discussed and counter-commented van der Helm's comments on our previous paper (Pinna and Conti, Brain Sci., 2019, 9, 149), where we demonstrated unique and relevant visual properties imparted by contrast polarity in eliciting amodal completion. The main question we addressed was: "What is the role of shape formation and perceptual organization in inducing amodal completion?" To answer this question, novel stimuli were studied through Gestalt experimental phenomenology. The results demonstrated the domination of the contrast polarity against good continuation, T-junctions, and regularity. Moreover, the limiting conditions explored revealed a new kind of junction next to the T- and Y-junctions, respectively responsible for amodal completion and tessellation. We called them I-junctions. The results were theoretically discussed in relation to the previous approaches and in the light of the phenomenal salience imparted by contrast polarity. In counter-commenting van der Helm's comments we went into detail of his critiques and rejected all of them point-by-point. We proceeded by summarizing hypotheses and discussion of the previous work, then commenting on each critique through old and new phenomena and clarifying the meaning of our previous conclusions.

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Peripheral word recognition is impaired by crowding, the harmful influence of surrounding objects (flankers) on target identification. Crowding is usually weaker when the target and the flankers differ (for example in color). Here, we investigated whether reducing crowding at syllable boundaries improved peripheral word recognition. In Experiment 1, a target letter was flanked by single letters to the left and right and presented at 8° in the lower visual field. Target and flankers were either the same or different in regard to contrast polarity, color, luminance, and combined color/luminance. Crowding was reduced when the target differed from the flankers in contrast polarity, but not in any of the other conditions. Using the same color and luminance values as in Experiment 1, we measured recognition performance (speed and accuracy) for uniform (e.g., all letters black), congruent (e.g., alternating black and white syllables), and incongruent (e.g., alternating black and white non-syllables) words in Experiment 2. Participants verbally reported the target word, briefly displayed at 8° in the lower visual field. Congruent and incongruent words were recognized slower compared to uniform words in the opposite contrast polarity condition, but not in the other conditions. Our results show that the same feature contrast between the target and the flankers that yielded reduced crowding, deteriorated peripheral word recognition when applied to syllables and non-syllabic word parts. We suggest that a potential advantage of reduced crowding at syllable boundaries in word recognition is counteracted by the disruption of word uniformity.

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PURPOSE: To assess the changes in the accommodative response of the eye while reading a text under different contrast polarity conditions: black letters on white background (BoW condition) and white letters on black background (WoB condition). METHODS: Eighteen subjects with ages ranging from 21 to 41 years participated in this experimental study. The accommodative response (AR) of the eye while reading a text with BoW or WoB contrast polarity was obtained objectively with an adaptive optics system that corrected all aberrations but subject's own. Two different letter sizes (visual acuity conditions), shown on a microdisplay, were tested. The AR of each eye was measured with its natural pupil diameter at 0-3D of accommodative demand from the far point of the eye, with a step of 0.5D. The slope of the stimulus-response curve was calculated for each subject and condition. RESULTS: The averaged maximum pupil size was bigger for reverse (WoB) than for normal (BoW) contrast with statistical significance. The slopes for the ARs of the four conditions were not significantly different from each other. CONCLUSIONS: Contrast polarity does not seem to influence the accommodative response when reading text from an electronic microdisplay.

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We compare two versions of two known phenomena, the Curvature blindness and the Kite mesh illusions, to highlight how similar manipulations lead to blindness to curvature and blindness to illusory curvature, respectively. The critical factor is a change in luminance polarity; this factor interferes with the computation of curvature along the contour, for both real and illusory curvature.

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The visual system can represent a partially occluded 3-D surface from images of separated surface segments. The underlying amodal surface integration process accomplishes this by amodally extending each surface segment behind the occluder (amodal surface extension) and integrating the extended surfaces to form a whole surface representation. We conducted five experiments to investigate how depth cues, such as binocular disparity, half-occlusion, and monocular depth cues (T-junctions and L-junctions), contribute to amodal surface extension, and how the geometrical relationship and image similarity among the surface segments affect surface integration. This was achieved by having observers adjust the stereoscopic depth and slant of a comparison stimulus to match those of the tested 3-D stimulus. We found that both binocular disparity and half-occlusion cues are used to determine border-ownership assignment of surface segments and for amodal surface extension. We also found that separated surface segments need to have the same luminance contrast-polarity for them to be integrated as a whole surface. Finally, we found that having the same motion direction, minimum misalignment between boundary contours, and proximity among separated segments facilitate their integration. Overall, our findings reveal a set of "perceptual factors" for amodal surface integration, which arguably reflects our visual system's built-in knowledge of the regularities in natural scenes.

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The maintenance of visual acuity during active and passive body motion is ensured by gaze-stabilizing reflexes that aim at minimizing retinal image slip. For the optokinetic reflex (OKR), large-field visual motion of the surround forms the essential stimulus that activates eye movements. Properties of the moving visual world influence cognitive motion perception and the estimation of visual image velocity. Therefore, the performance of brainstem-mediated visuo-motor behaviors might also depend on image scene characteristics. Employing semi-intact preparations of mid-larval stages of Xenopus laevis tadpoles, we studied the influence of contrast polarity, intensity, contour shape and different motion stimulus patterns on the performance of the OKR and multi-unit optic nerve discharge during motion of a large-field visual scene. At high contrast intensities, the OKR amplitude was significantly larger for visual scenes with a positive contrast (bright dots on a dark background) compared with those with a negative contrast. This effect persisted for luminance-matched pairs of stimuli, and was independent of contour shape. The relative biases of OKR performance along with the independence of the responses from contour shape were closely matched by the optic nerve discharge evoked by the same visual stimuli. However, the multi-unit activity of retinal ganglion cells in response to a small single moving vertical edge was strongly influenced by the light intensity in the vertical neighborhood. This suggests that the underlying mechanism of OKR biases related to contrast polarity directly derives from visual motion-processing properties of the retinal circuitry.

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Visual prostheses require an effective representation method due to the limited display condition which has only 2 or 3 levels of grayscale in low resolution. Edges derived from abrupt luminance changes in images carry essential information for object recognition. Typical binary (black and white) edge images have been used to represent features to convey essential information. However, in scenes with a complex cluttered background, the recognition rate of the binary edge images by human observers is limited and additional information is required. The polarity of edges and cusps (black or white features on a gray background) carries important additional information; the polarity may provide shape from shading information missing in the binary edge image. This depth information may be restored by using bipolar edges. We compared object recognition rates from 16 binary edge images and bipolar edge images by 26 subjects to determine the possible impact of bipolar filtering in visual prostheses with 3 or more levels of grayscale. Recognition rates were higher with bipolar edge images and the improvement was significant in scenes with complex backgrounds. The results also suggest that erroneous shape from shading interpretation of bipolar edges resulting from pigment rather than boundaries of shape may confound the recognition.

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The human brain rapidly detects faces in the visual environment. We recently presented a sweep visual evoked potential approach to objectively define face detection thresholds as well as suprathreshold response functions (Ales, Farzin, Rossion, & Norcia, 2012). Here we determined these parameters are affected by orientation (upright vs. inverted) and contrast polarity (positive vs. negative), two manipulations that disproportionately disrupt the perception of faces relative to other object categories. Face stimuli parametrically increased in visibility through phase-descrambling while alternating with scrambled images at a fixed presentation rate of 3 Hz (6 images/s). The power spectrum and mean luminance of all stimuli were equalized. As a face gradually emerged during a stimulation sequence, EEG responses at 3 Hz appeared at ≈35% phase coherence over right occipito-temporal channels, replicating previous observations. With inversion and contrast-reversal, the 3-Hz amplitude decreased by ≈20%-50% and the face detection threshold increased by ≈30%-60% coherence. Furthermore, while the 3-Hz response emerged abruptly and saturated quickly for normal faces, suggesting a categorical neural response, the response profile for inverted and negative polarity faces was shallower and more linear, indicating gradual and continuously increasing activation of the underlying neural population. These findings demonstrate that inversion and contrast-reversal increase the threshold and modulate the suprathreshold response function of face detection.

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Visual contours often result from the integration or interpolation of fragmented edges. The strength of the completion increases when the edges share the same contrast polarity (CP). Here we demonstrate that the appearance in the perceptual field of this integrated unit, or contour of invariant CP, is concomitant with a vivid brightness alteration of the surfaces at its opposite sides. To observe this effect requires some stratagems because the formation in the visual field of a contour of invariant CP normally engenders the formation of a second contour and then the rise of two streams of induction signals that interfere in different ways. Particular configurations have been introduced that allow us to observe the induction effects of one contour taken in isolation. I documented these effects by phenomenological observations and psychophysical measurement of the brightness alteration in relation to luminance contrast. When the edges of the same CP complete to form a contour, the background of homogeneous luminance appears to dim at one side and to brighten at the opposite side (in accord with the CP). The strength of the phenomenon is proportional to the local luminance contrast. This effect weakens or nulls when the contour of the invariant CP separates surfaces filled with different gray shades. These conflicting results stimulate a deeper exploration of the induction phenomena and their role in the computation of brightness contrast. An alternative perspective is offered to account for some brightness illusions and their relation to the phenomenal transparency. The main assumption asserts that, when in the same region induction signals of opposite CP overlap, the filling-in is blocked unless the image is stratified into different layers, one for each signal of the same polarity. Phenomenological observations document this "solution" by the visual system.

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PURPOSE: (1) To devise a model-based method for estimating the probabilities of binocular fusion, interocular suppression and diplopia from psychophysical judgements, (2) To map out the way fusion, suppression and diplopia vary with binocular disparity and blur of single edges shown to each eye, (3) To compare the binocular interactions found for edges of the same vs opposite contrast polarity. METHODS: Test images were single, horizontal, Gaussian-blurred edges, with blur B = 1-32 min arc, and vertical disparity 0-8.B, shown for 200 ms. In the main experiment, observers reported whether they saw one central edge, one offset edge, or two edges. We argue that the relation between these three response categories and the three perceptual states (fusion, suppression, diplopia) is indirect and likely to be distorted by positional noise and criterion effects, and so we developed a descriptive, probabilistic model to estimate both the perceptual states and the noise/criterion parameters from the data. RESULTS: (1) Using simulated data, we validated the model-based method by showing that it recovered fairly accurately the disparity ranges for fusion and suppression, (2) The disparity range for fusion (Panum's limit) increased greatly with blur, in line with previous studies. The disparity range for suppression was similar to the fusion limit at large blurs, but two or three times the fusion limit at small blurs. This meant that diplopia was much more prevalent at larger blurs, (3) Diplopia was much more frequent when the two edges had opposite contrast polarity. A formal comparison of models indicated that fusion occurs for same, but not opposite, polarities. Probability of suppression was greater for unequal contrasts, and it was always the lower-contrast edge that was suppressed. CONCLUSIONS: Our model-based data analysis offers a useful tool for probing binocular fusion and suppression psychophysically. The disparity range for fusion increased with edge blur but fell short of complete scale-invariance. The disparity range for suppression also increased with blur but was not close to scale-invariance. Single vision occurs through fusion, but also beyond the fusion range, through suppression. Thus suppression can serve as a mechanism for extending single vision to larger disparities, but mainly for sharper edges where the fusion range is small (5-10 min arc). For large blurs the fusion range is so much larger that no such extension may be needed.

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Human can easily detect other's eyes and gaze from early in life. Such sensitivity is supported by the contrast polarity of human eyes, which have a white sclera contrasting with the darker colored iris (Kobayashi & Kohshima, (1997). Nature, 387, 767-768; Kobayashi & Kohshima, (2001). Journal of Human Evolution, 40, 419-435). Recent studies suggest that the contrast polarity around the eyes plays an important role in infants' face processing. Newborns preferred upright face images to inverted ones in contrast-preserved faces, but not in contrast-reversed faces (Farroni et al., (2005). Proceedings of National Academy of Sciences of the United States of America, 102, p. 17245-17250). Seven- to 8-month-old infants failed to discriminate between faces when the contrast polarity of eyes was reversed (Otsuka et al., (2013). Journal of Experimental Child Psychology, 115, 598-606). Neuroimaging study with adults revealed that full-negative faces induced less activation in the right fusiform gyrus than either full-positive faces or negative faces with contrast-preserved eyes (Gilad et al., (2009). Proceedings of National Academy of Sciences of the United States of America, 106, p. 5353-5358). In the present study, we investigated whether contrast-reversed eyes diminish infants' brain activity related to face processing. We measured hemodynamic responses in the bilateral temporal area of 5- to 6-month-old infants. Their hemodynamic responses to faces with positive eyes and those with negative eyes were compared against the baseline activation during the presentation of object images. We found that the presentation of faces with positive eyes increased the concentration of oxy-Hb in the right temporal area and those of total-Hb in the bilateral temporal areas. No such change occurred for faces with negative eyes. Our results suggest the importance of contrast polarity of the eyes in the face-selective neural responses from early development.

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Color filling-in is the phenomenon in which the color of a visual area is perceived as the color that is only presented in an adjacent area. In a stimulus with multiple edges, color filling-in can occur along any edge and in both centripetal and centrifugal directions when maintaining steady fixation. The current study aimed to investigate the role of chromatic contrast magnitude and polarity along the two chromaticity cardinal axes and the interaction of the axes in the color filling-in process. In Experiment 1, the color filling-in process was examined using stimuli with three different regions and two edges. The three regions had chromaticities that varied only in one of the chromaticity axes. In Experiment 2, the regions along both edges differed in chromaticity along both axes. The results showed that the contrast magnitudes and polarity relationship of the two edges worked together to determine the filled-in direction and time course of the filled-in percepts. Further, the results pointed to a common mechanism mediating the color filling-in process along the two cardinal axes, and the two axes did not act independently in this process.

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After prolonged exposure to a distorted face with expanded or contracted inner features, a subsequently presented normal face appears distorted toward the opposite direction. This phenomenon, termed as face distortion aftereffect (FDAE), is thought to occur as a result of changes in the mechanisms involved in higher order visual processing. However, the extent to which FDAE is mediated by face-specific configural processing is less known. In the present study, we investigated whether similar aftereffects can be induced by stimuli lacking all the typical characteristics of a human face except for its first-order configural properties. We found a significant FDAE after adaptation to a stimulus consisting of three white dots arranged in a triangular fashion and placed in a gray oval. FDAEs occurred also when the adapting and test stimuli differed in size or when the contrast polarity of the adaptor image was changed. However, the inversion of the adapting image as well as the reduction of its contrast abolished the aftereffect entirely. Taken together, our results suggest that higher-level visual areas, which are involved in the processing of facial configurations, mediate the FDAE. Further, while adaptation seems to be largely invariant to contrast polarity, it appears sensitive to orientation and to lower level manipulations that affect the saliency of the inner features.

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Scene segmentation depends on interaction between geometrical and photometric factors. It has been shown that reversals in contrast polarity at points of highest orientation discontinuity along closed contours significantly impair shape discrimination performance, while changes in contrast polarity at straight(er) contour segments do not have such deleterious effects (Spehar, 2002). Here we employ (semi) high resolution fMRI (1.5 mm × 1.5 mm × 1.5 mm) to investigate the neuronal substrate underlying these perception effects. Stimuli consisted of simple elements (a) squares with contrast reversals along straight segments; (b) squares with contrast reversals in the corner (highest orientation discontinuity); (c) L-Junctions with contrast reversals along the straight ends; (d) L-Junctions with contrast reversals in the corner. Element with contrast polarity reversals are easy to distinguish though appear geometrically equivalent. For squares with contrast polarity reversals only along straight lines we find significantly lower BOLD modulation compared to any of the control conditions, which show similar responses to each other. In the light of previous psychophysical work (Elder and Zucker, 1993; Spehar, 2002) we speculate that this effect is due to closure perception. We observe this across a wide range of areas on occipital cortex.