Perceptual constancy during ocular pursuit: a quantitative estimation procedure

Perceptual constancy of visual motion is usually described as the degree of correspondence between physical and perceived characteristics of motion in the external world. To study it, one has to assess the relationship between physical motion, its retinal image, and its perception. We describe a quantitative estimation procedure for a measure K denoting the degree of perceptual constancy of background target motions noncollinear to the eye movements during ocular pursuit. The calculation of K is based on three vectors describing the target motion (1) as it is physically, (2) as it is mapped to the retina, and (3) as it is perceived, but only the direction of the perceptual motion vector has to be determined experimentally. K allows for quantitative comparison between experiments with a variety of parameters in visual motion displays.     

Visual perception and corollary discharge

Perception depends not only on sensory input but also on the state of the brain receiving that input. A classic example is perception of a stable visual world in spite of the saccadic eye movements that shift the images on the retina. A long-standing hypothesis is that the brain compensates for the disruption of visual input by using advance knowledge of the impending saccade, an internally generated corollary discharge. One possible neuronal mechanism for this compensation has been previously identified in parietal and frontal cortex of monkeys, but the origin of the necessary corollary discharge remained unknown. Here, we consider recent experiments that identified a pathway for a corollary discharge for saccades that extends from the superior colliculus in the midbrain to the frontal eye fields in the cerebral cortex with a relay in the medial dorsal nucleus of the thalamus. We first review the nature of the evidence used to identify a corollary discharge signal in the complexity of the primate brain and show its use for guiding a rapid sequence of eye movements. We then consider two experiments that show this same corollary signal may provide the input to the frontal cortex neurons that alters their activity with saccades in ways that could compensate for the displacements in the visual input produced by saccadic eye movements. The first experiment shows that the corollary discharge signal is spatially and temporally appropriate to produce the alterations in the frontal-cortex neurons. The second shows that this signal is necessary for this alteration because inactivation of the corollary reduces the compensation by frontal-cortex neurons. The identification of this relatively simple circuit specifies the organization of a corollary discharge in the primate brain for the first time and provides a specific example upon which consideration of the roles of corollary activity in other systems and for other functions can be evaluated.     

Perceptual constancy during ocutar pursuit: A quantitative estimation procedure

Perceptual constancy of uisual motion is usually described as the degree of correspondence between physical and perceived characteristics of motion in the external world. To study it, one has to assess the relationship between physical motion, its retinal image, and its perception. We describe a quantitative estimation procedure for a measure K denoting the degree of perceptual constancy of background target motions noncollinear to the eye movements during ocular pursuit. The calculation of K is based on three vectors describing the target motion (1) as it is physically, (2) as it is mapped to the retina, and (3) as it is perceived, but only the direction of the perceptual motion vector has to be determined experimentally. K allows for quantitative comparison between experiments with a variety of parameters in visual motton displays.     

What Eye Movements Reveal About Later Comprehension of Long Connected Texts

We know that reading involves coordination between textual characteristics and visual attention, but research linking eye movements during reading and comprehension assessed after reading is surprisingly limited, especially for reading long connected texts. We tested two competing possibilities: (a) the weak association hypothesis: Links between eye movements and comprehension are weak and short-lived, versus (b) the strong association hypothesis: The two are robustly linked, even after a delay. Using a predictive modeling approach, we trained regression models to predict comprehension scores from global eye movement features, using participant-level cross-validation to ensure that the models generalize across participants. We used data from three studies in which readers (Ns = 104, 130, 147) answered multiple-choice comprehension questions ~30 min after reading a 6,500-word text, or after reading up to eight 1,000-word texts. The models generated accurate predictions of participants' text comprehension scores (correlations between observed and predicted comprehension: 0.384, 0.362, 0.372, ps < .001), in line with the strong association hypothesis. We found that making more, but shorter fixations, consistently predicted comprehension across all studies. Furthermore, models trained on one study's data could successfully predict comprehension on the others, suggesting generalizability across studies. Collectively, these findings suggest that there is a robust link between eye movements and subsequent comprehension of a long connected text, thereby connecting theories of low-level eye movements with those of higher order text processing during reading.     

Two kinds of adaptation in the constancy of visual direction and their different effects on the perception of shape and visual direction

Adaptation in the constancy of visual direction can be obtained under two radically different conditions, called eye-movement adaptation and field adaptation. Adaptation resulting from these conditions and from a “normal” condition was measured with a newly developed estimation test. Eye-movement adaptation was found to cause an alteration of compensatory eye movements. It apparently consists of a changed evaluation of eye movements, as demonstrated by two different pointing tests. A form test where the shape of a large oblong is set to look square also confirmed this interpretation. After field adaptation, a pointing test did not register a change, but an adaptation effect could be measured with a forward direction test. This test and a square test where no eye movements were permitted proved to be specific to field adaptation; they measured no effect after eye-movementadaptation. The normal adaptation condition Was apparently equivalent to the eye-movement adaptation condition. Its effect could be measured only with a pointing test. When we changed the normal adaptation condition so that frequent saccades were made during head turning, strong effects were measured with the two tests that were specific to field adaptation.     

Cardiac-somatic coupling during the foreperiod in a simple reaction-time task

The cardiac-somatic coupling hypothesis predicts a phasic decrease of general somatic behavior concomitant with a phasic heart-rate deceleration. This hypothesis was investigated during a constant 4 s foreperiod (FP) in a simple auditory reaction-time task. Intertrial interval duration was variable (mean 15.5 s; range 11–20 s). The response was a plantar flexion of the right foot. Besides ECG and EOG, surface EMG of nine striate muscles varying in relevance to response execution was recorded.In agreement with the hypothesis, heart rate, eye movements, and m. mylohyoideus EMG were decreased at the end of the FP. An increase in the EMG of the agonist m. soleus, antagonist m. tibialis anterior, m. peroneus longus, and m. trapezius was found during the FP. The activity in all other response-irrelevant muscles did not significantly differ from baseline. It was concluded that the results are at variance with the cardiac-somatic coupling hypothesis. Changes in surface EMG are discussed in terms of motor preparation.     

Localization of targets across saccades: Role of landmark objects

Saccadic eye movements are required to bring different parts of the visual world into the foveal region of the retina. With each saccade, the images of the objects drastically change their retinal positions—nevertheless, the visual world appears continuous and does not seem to jump. How does the visual system achieve this continuous and stable percept of the visual world, despite the gross changes of its retinal projection that occur with each saccade? The present paper argues that an important factor of this type of space constancy is formed by the reafferent information, i.e., the visual display that is found when the eyes land. Three experiments demonstrate that objects present across the saccade can serve as landmarks for postsaccadic relocalization. The basic experimental manipulation consisted of a systematic displacement of these landmark objects during the saccade. The effectiveness of the landmarks was determined by analysing to what degree they modify the perceived shift of a small saccade target that was blanked for 200 ms during and after the saccade. A first experiment studied the spatial range where objects become effective as landmarks. The data show that landmarks close to the saccade target and horizontally aligned with the target are specifically effective. The second experiment demonstrates that postsaccadic localization is normally based on relational information about relative stimulus positions transferred across the saccade. A third experiment studied the effect of a prominent background frame on transsaccadic localization; the results suggest that background structures contribute only little to transsaccadic localization.     

Predictive remapping gives rise to environmental inhibition of return

Neurons in various brain regions predictively respond to stimuli that will be brought to their receptive fields by an impending eye movement. This neural mechanism, known as predictive remapping, has been suggested to underlie spatial constancy. Inhibition of return (IOR) is a bias against recently attended locations. The present study examined whether predictive remapping is a mechanism underlying IOR effects observed in environmental coordinates. The participant made saccades to a peripheral location after an IOR effect had been elicited by an onset cue and discriminated a target presented around the time of saccade onset. Immediately before the required saccade, IOR emerged at the retinal locus that would be brought to the cued location. A second task in which the participant maintained fixation during the entire trial ruled out the possibility that this IOR effect was simply the spillover of IOR from the cued location. These findings, for the first time, provide direct behavioral evidence that predictive remapping is a mechanism underlying environmental IOR.     

Visual spatial constancy and modularity: Does intention penetrate vision?

Is vision informationally encapsulated from cognition or is it cognitively penetrated? I shall argue that intentions penetrate vision in the experience of visual spatial constancy: the world appears to be spatially stable despite our frequent eye movements. I explicate the nature of this experience and critically examine and extend current neurobiological accounts of spatial constancy, emphasizing the central role of motor signals in computing such constancy. I then provide a stringent condition for failure of informational encapsulation that emphasizes a computational condition for cognitive penetration: cognition must serve as an informational resource for visual computation. This requires proposals regarding semantic information transfer, a crucial issue in any model of informational encapsulation. I then argue that intention provides an informational resource for computation of visual spatial constancy. Hence, intention penetrates vision.     

Two kinds of adaptation in the constancy of visual direction

Adaptation in the constancy of visual direction had previously been obtained by causing a large or a small visible area representing the environment to be objectively displaced in dependence on head movements. No stationary objects were permitted to be visible. Now experiments are reported in which displacements of a large patterned field, with the subject fixating a stationary mark in its center, led to adaptation. In these experiments, objective displacements of the environment were given by image displacements on the retina. Adaptation also resulted when the large field was stationary and only the fixation mark was displaced. Here the objective displacement was given by the rate of pursuit eye movements.     

The effect of abnormal displacement of the retinal image during eye movements

The displacement of the images on the retina that results from a turning of the eye does not lead to an apparent motion of what is seen, It has been generally assumed that this is due to a compensating process which takes eye movement into account and serves to discount those image displacements that result from eye movements, It follows from this view that an abnormal image displacement, that is, an image displacement that is larger or smaller than the causing eye movement would warrant, should lead to an experienced displacement of the target. Abnormal image displacement was produced by placing the eye in the converging or diverging bundle of rays from a point source that form behind a strong positive lens; this arrangement yielded a disc-shaped image, the projection of the pupil onto the retina, which displaced abnormally during eye movements. By changing the position of the eye along the axis of the lens in relation to the crossing point of the bundle, the degree to which the displacement was abnormal could be varied, For various displacement rates ranging from 25% to 120 and 400% of normal, abnormal displacements produced by incidental eye movements remained unnoticed, Only where eye movements were intentional did some of our Ss report shifts of the perceived image. It is suggested that the organism copes with the image displacement resulting from the ever-present incidental eye movements not by compensation but by ignoring them.     

Gradual remapping results in early retinotopic and late spatiotopic inhibition of return

Here we report that immediately following the execution of an eye movement, oculomotor inhibition of return resides in retinotopic (eye-centered) coordinates. At longer postsaccadic intervals, inhibition resides in spatiotopic (world-centered) coordinates. These results are explained in terms of perisaccadic remapping. In the interval surrounding an eye movement, information is remapped within retinotopic maps to compensate for the retinal displacement. Because remapping is not an instantaneous process, a fast, but gradual, transfer of inhibition of return from retinotopic to spatiotopic coordinates can be observed in the postsaccadic interval. The observation that visual stability is preserved in inhibition of return is consistent with its function as a "foraging facilitator," which requires locations to be inhibited across multiple eye movements. The current results support the idea that the visual system is retinotopically organized and that the appearance of a spatiotopic organization is due to remapping of visual information to compensate for eye movements.     

Memory for retinotopic locations is more accurate than memory for spatiotopic locations,even for visually guided reaching

To interact successfully with objects, we must maintain stable representations of their locations in the world. However, their images on the retina may be displaced several times per second by large, rapid eye movements. A number of studies have demonstrated that visual processing is heavily influenced by gaze-centered (retinotopic) information, including a recent finding that memory for an object’s location is more accurate and precise in gaze-centered (retinotopic) than world-centered (spatiotopic) coordinates (Golomb & Kanwisher, 2012b). This effect is somewhat surprising, given our intuition that behavior is successfully guided by spatiotopic representations. In the present experiment, we asked whether the visual system may rely on a more spatiotopic memory store depending on the mode of responding. Specifically, we tested whether reaching toward and tapping directly on an object’s location could improve memory for its spatiotopic location. Participants performed a spatial working memory task under four conditions: retinotopic vs. spatiotopic task, and computer mouse click vs. touchscreen reaching response. When participants responded by clicking with a mouse on the screen, we replicated Golomb & Kanwisher’s original results, finding that memory was more accurate in retinotopic than spatiotopic coordinates and that the accuracy of spatiotopic memory deteriorated substantially more than retinotopic memory with additional eye movements during the memory delay. Critically, we found the same pattern of results when participants responded by using their finger to reach and tap the remembered location on the monitor. These results further support the hypothesis that spatial memory is natively retinotopic; we found no evidence that engaging the motor system improves spatiotopic memory across saccades.     

Sources of position-perception error for small isolated targets

It has often been reported that, in the presence of static reference stimuli, briefly presented visual targets are perceived as being closer to the fixation point than they actually are. The first purpose of the present study was to investigate whether the same phenomenon can be demonstrated in a situation without static reference stimuli. Experiment 1, with position naming as the task, showed that such a central shift is also observed under these conditions. This finding is of importance because it completes an explanation for central near-location errors in the partial-report bar-probe task. The second purpose of the present study was to provide an explanation for these central shifts. For this explanation information about the exact size of the central shift is required. In Exps. 2, 3, and 4, with cursor setting as the task, it was attempted to assess more precisely the size of the central shifts. These experiments revealed that two different factors determine the results in cursor setting tasks; a factor “target position” and a factor “cursor position.” Experiment 5 showed that it is the point of fixation, not the fixation point, that serves, at least in part, as the reference point in this type of task. All the findings together allow us to conclude that the target positions are underestimated by about 10%. From vision research it is known that saccadic eye movements, performed for bringing a target in the fovea, also show an undershoot of about 10%. It is therefore concluded that the system in charge of saccadic eye movements also provides the metric in visual space within a single eye fixation. Received: 11 February 1998 / Accepted: 25 June 1998     

Magnitude scales,category scales,and the general psychophysical differential equation

The general psychophysical differential equation (GPDE) which relates scale values and Weber functions for two subjective variables was tested statistically with data from a number of category rating and magnitude estimation experiments. In all tests. it was investigated whether the GPDE is compatible with the assumption that the Weber function of the category scale is constant. This assumption implies that the category scale may be regarded as a discrimination scale. The tests were carried out by estimating the Weber function of the category scale by means of the GPDE and testing these estimates for constancy, For group data, there were fairly small systematic deviations from constancy across different experiments in the Weber functions that were estimated by the GPDE, and the hypothesis of a constant estimated Weber function could not be rejected statistically (p>.05) in most experiments. For individual data the estimated Weber functions deviated from constancy in idiosyncratic ways, and these deviations were statistically significant (p<.05)for most subjects.     

What is Pragmatism in Brazil Today?

This paper analyses the relations between Pragmatism and Brazilian culture, nowadays defined as a plural culture. It shows that the introduction of Pragmatism into Brazilian educational movements in the past actually made such culture much more receptive to pragmatist ideas. After discussing the concepts of truth and minimalism on Richard Rorty’s Philosophical Papers, the authors conclude that Brazilian education today is receptive to the conception in which new narratives can be used as a powerful instrument to change the world.     

Context effects in visual length perception: role of ocular,retinal, and spatial location

In three experiments, we examined the transfer of orientation-contingent context effects between the eyes and across portions of the retina with or without variation in external spatial location. Previous research had shown that vertical lines are judged long, relative to horizontal lines, when the stimulus set comprises relatively long horizontals and short verticals (Contextual Condition B), as compared with the reverse when the stimulus set comprises relatively short horizontals and long verticals (Contextual Condition A). Consequently, the contextual set of stimuli influences the magnitude of the horizontal-vertical illusion (HVI), decreasing its size under Contextual Condition A and increasing its size under Contextual Condition B. Experiment 1 showed that exposing one eye to different stimulus contexts modulated the size of the HVI at the exposed eye but had little or no effect at the other eye. Experiments 2 and 3 showed that the effect of the contextual sets generalized poorly across adjacent portions of the retina but transferred almost perfectly across different locations in external space when retinal location was constant. Thus, orientation-contingent context effects in visual length perception appear to be specific to the eye and to the region of the retina stimulated, suggesting that these effects reflect relatively early and local changes in sensitivity, rather than relatively late and general shifts in response criteria.     

Gesturing during mental problem solving reduces eye movements,especially for individuals with lower visual working memory capacity

Non-communicative hand gestures have been found to benefit problem-solving performance. These gestures seem to compensate for limited internal cognitive capacities, such as visual working memory capacity. Yet, it is not clear how gestures might perform this cognitive function. One hypothesis is that gesturing is a means to spatially index mental simulations, thereby reducing the need for visually projecting the mental simulation onto the visual presentation of the task. If that hypothesis is correct, less eye movements should be made when participants gesture during problem solving than when they do not gesture. We therefore used mobile eye tracking to investigate the effect of co-thought gesturing and visual working memory capacity on eye movements during mental solving of the Tower of Hanoi problem. Results revealed that gesturing indeed reduced the number of eye movements (lower saccade counts), especially for participants with a relatively lower visual working memory capacity. Subsequent problem-solving performance was not affected by having (not) gestured during the mental solving phase. The current findings suggest that our understanding of gestures in problem solving could be improved by taking into account eye movements during gesturing.     

Guiding Decision Makers' Eye Movements with (Un)Predictable Object Locations

We propose a new approach for guiding eye movements by controlling the predictability of object locations. We hypothesize that when a high (low) relevance object has a predictable location, observers are more (less) likely to fixate it compared with objects in unpredictable locations. We tested this hypothesis in three decision‐making studies, manipulating the location of a product label in an unpredictable, a predictable, and a mixed visual environment. In Study 1 and Study 2, we find that participants are less likely to fixate a low and medium relevance label in a predictable location, and in Study 3, we find that participants are more likely to fixate a high relevance label in a predictable location. Our findings suggest that predictable locations increase while unpredictable locations decrease top‐down control. The approach can be used to increase or decrease eye movements towards specific information depending on the goals of the choice architect. Copyright © 2017 John Wiley & Sons, Ltd.     

The absence of depth constancy in contour stereograms

Stereoscopic surfaces constructed from Kanizsa-type illusory contours or explicit luminance contours were tested for three-dimensional (3-D) shape constancy. The curvature of the contours and the apparent viewing distance between the surface and the observer were manipulated. Observers judged which of two surfaces appeared more curved. Experiment 1 allowed eye movements and revealed a bias in 3-D shape judgment with changes in apparent viewing distance, such that surfaces presented far from the observer appeared less curved than surfaces presented close to the observer. The lack of depth constancy was approximately the same for illusory-contour surfaces and for explicit-contour surfaces. Experiment 2 showed that depth constancy for explicit-contour surfaces improved slightly when fixation was required and eye movements were restricted. These experiments suggest that curvature in depth is misperceived, and that illusory-contour surfaces are particularly sensitive to this distortion.