Moving window generator for reading experiments

An inexpensive PC-based moving window generator with an eye movement recording system is described. The moving window technique, activated by current eye movements, has an advantage over the fixed window technique in measuring the effective visual field size during reading. A variable rectangular window, through which the subject observes the text, is generated on a PC-controlled CRT screen. The system includes a frame buffer memory, an analog-to-digital conversion unit, and an eye movement recording system. The system works well for measuring approximate field size during reading.     

Brightness exponent as a function of retinal eccentricity in the peripheral visual field: Effects of dark and light adaptation

Using a method of direct magnitude estimation, the exponent of the brightness power function was determined under dark and light adaptation at luminance levels well above threshold. The exponent was estimated for functions describing the brightness of stimuli presented at the fovea and the following peripheral retinal loci: 10, 20, 30, 40, and 50 deg nasally eccentric to the fovea along the horizontal meridian of the right eye. The exponent for a 1-sec flash was found to be approximately .33 at the fovea and increased slightly with increasing retinal eccentricity.The effect of adaptation on the brightness exponent was not so large when the target luminance was set well above threshold.     

An inexpensive microcomputer peripheral I/O expansion

Using a one-chip programmable peripheral interface LSI (8255A), an inexpensive micro-computer (8K PET) peripheral I/O expansion can easily be constructed.     

Individual differences in working memory during reading with and without parafoveal information: a moving-window study

We examined individual differences in working memory appearing in the effective visual field size while reading Japanese text. Working memory capacity was measured by a Japanese reading span test, and the subjects were divided into high- and low-score groups. Reading performance was measured by reading time, comprehension, and eye movements using a variable moving window through which the subject could read areas of the Japanese text. As the window size decreased, the reading time increased significantly. High-span subjects showed better performance in reading time, comprehension, and fixation duration than low-span subjects even in small visual fields. Interestingly, high-span subjects appear to show better information integration during reading, whereas low-span subjects showed less integration without parafoveal vision. These findings suggest that reading performance was better for subjects with larger working memory resources in a parafoveal restriction condition.     

An unsupported common view: Comparing Japan and the U.S. on individualism/collectivism

It has long been believed that the Japanese are more collectivistic than the Americans. To assess the validity of this common view, we reviewed 15 empirical studies that compared these two nations on individualism/collectivism. Surprisingly, 14 studies did not support the common view; the only study that supported it turned out to bear little relevance to the ordinary definition of individualism/collectivism. An examination of the supportive evidence of the common view disclosed that this view had been formed on an unexpectedly flimsy ground. It further turned out that the wide acceptance of the common view may have been the result of the fundamental attribution error, which may have led to an underestimation of situational factors in interpreting the past obviously collectivistic behavior of the Japanese.     

Spatial imagery of novel places based on visual scene transformation

The hippocampus is known to maintain memories of object-place associations that can produce a scene expectation at a novel viewpoint. To implement such capabilities, the memorized distances and directions of an object from the viewer at a fixed location should be integrated with the imaginary displacement to the new viewpoint. However, neural dynamics of such scene expectation at the novel viewpoint have not been discussed. In this study, we propose a method of coding novel places based on visual scene transformation as a component of the object-place memory in the hippocampus. In this coding, a novel place is represented by a transformed version of a viewer’s scene with imaginary displacement. When the places of individual objects are stored with the coding in the hippocampus, the object’s displacement at the imaginary viewpoint can be evaluated through the comparison of a transformed viewer’s scene with the stored scene. Results of computer experiments demonstrated that the coding successfully produced scene expectation of a three object arrangement at a novel viewpoint. Such the scene expectation was retained even without similarities between the imaginary scene and the real scene at the location, where the imaginary scenes only functioned as indices to denote the topographical relationship between object locations. The results suggest that the hippocampus uses the place coding based on scene transformation and implements the spatial imagery of object-place associations from the novel viewpoint.     

Target size and luminance in apparent brightness of the peripheral visual field.

Four target sizes between 15 and 120 min. of arc with six luminance levels covering the range between 398.1 and 1.26 cd/m2 in steps of .5 log units were presented to 0, 20, 40, 60, and 80 degrees nasal retinal loci. In both peripheral and foveal viewing, magnitude estimates to apparent brightness judged by 12 Ss changed as a function of target size and luminance. The exponent of the power function was not dependent on retinal loci but on target size. However, when target size increased, the apparent brightness was slightly greater with peripheral viewing than with foveal viewing.     

Recovery from object substitution masking induced by transient suppression of visual motion processing: a repetitive transcranial magnetic stimulation study

Object substitution masking is a form of visual backward masking in which a briefly presented target is rendered invisible by a lingering mask that is too sparse to produce lower image-level interference. Recent studies suggested the importance of an updating process in a higher object-level representation, which should rely on the processing of visual motion, in this masking. Repetitive transcranial magnetic stimulation (rTMS) was used to investigate whether functional suppression of motion processing would selectively reduce substitution masking. rTMS-induced transient functional disruption of cortical area V5/MT+, which is important for motion analysis, or V1, which is reciprocally connected with V5/MT+, produced recovery from masking, whereas sham stimulation did not. Furthermore, masking remained undiminished following rTMS over the region 2 cm posterior to V5/MT+, ruling out nonspecific effects of real stimulation and confirming regional specificity of the rTMS effect. The results suggest that object continuity via the normal function of the visual motion processing system might in part contribute to this masking. The relation of these findings to the reentrant processing view of object substitution masking and other visual phenomena is discussed.     

Brightness exponent as a function of flash duration and retinal eccentricity

The effect of flash duration on the exponent of the brightness power function was investigated in the fovea and 20-deg periphery using a method of direct magnitude estimation. The flash duration employed covered a 5-log-unit range between .001 and 100 sec. The results showed that the exponent is clearly time-dependent for both extremes of the duration—that is, very short (.001 to .1 sec) and prolonged (3 to 100 sec) durations—but not for the medium flash durations between .1 and 3 sec. Furthermore, the exponent is a little larger for peripheral viewing than for foveal viewing except for the durations below approximately .03 sec. The systematic change of the exponent as a function of duration is discussed in terms of retinal and postretinal intensity coding functions.