ÐMany machine vision applications, such as compression, pictorial database querying, and image understanding, often need to analyze in detail only a representative subset of the image, which may be arranged into sequences of loci called regions-of-interest, ROIs. We have investigated and developed a methodology that serves to automatically identify such a subset of aROIs (algorithmically detected ROIs) using different Image Processing Algorithms, IPAs, and appropriate clustering procedures. In human perception, an internal representation directs top-down, context-dependent sequences of eye movements to fixate on similar sequences of hROIs (human identified ROIs). In this paper, we introduce our methodology and we compare aROIs with hROIs as a criterion for evaluating and selecting bottom-up, context-free algorithms. An application is finally discussed.
It has long been documented that emotional and sensory events elicit a pupillary dilation. Is the pupil response a reliable marker of a visual detection event while viewing complex imagery? In two experiments where viewers were asked to report the presence of a visual target during rapid serial visual presentation (RSVP), pupil dilation was significantly associated with target detection. The amplitude of the dilation depended on the frequency of targets and the time of target presentation relative to the start of the trial. Larger dilations were associated with trials having fewer targets and with targets viewed earlier in the run. We found that dilation was influenced by, but not dependent on, the requirement of a button press. Interestingly, we also found that dilation occurred when viewers fixated a target but did not report seeing it. We will briefly discuss the role of noradrenaline in mediating these pupil behaviors.
Dandekar S, Privitera C, Carney T, Klein SA. Neural saccadic response estimation during natural viewing. J Neurophysiol 107: 1776-1790, 2012. First published December 14, 2011 doi:10.1152/jn.00237.2011Studying neural activity during natural viewing conditions is not often attempted. Isolating the neural response of a single saccade is necessary to study neural activity during natural viewing; however, the close temporal spacing of saccades that occurs during natural viewing makes it difficult to determine the response to a single saccade. Herein, a general linear model (GLM) approach is applied to estimate the EEG neural saccadic response for different segments of the saccadic main sequence separately. It is determined that, in visual search conditions, neural responses estimated by conventional eventrelated averaging are significantly and systematically distorted relative to GLM estimates due to the close temporal spacing of saccades during visual search. Before the GLM is applied, analyses are applied that demonstrate that saccades during visual search with intersaccadic spacings as low as 100 -150 ms do not exhibit significant refractory effects. Therefore, saccades displaying different intersaccadic spacings during visual search can be modeled using the same regressor in a GLM. With the use of the GLM approach, neural responses were separately estimated for five different ranges of saccade amplitudes during visual search. Occipital responses time locked to the onsets of saccades during visual search were found to account for, on average, 79 percent of the variance of EEG activity in a window 90 -200 ms after the onsets of saccades for all five saccade amplitude ranges that spanned a range of 0.2-6.0 degrees. A GLM approach was also used to examine the lateralized ocular artifacts associated with saccades. Possible extensions of the methods presented here to account for the superposition of microsaccades in event-related EEG studies conducted in nominal fixation conditions are discussed. saccades; EEG; visual search; microsaccades; artifact removal EEG IS WELL SUITED FOR THE study of fast neural dynamics, and a variety of EEG studies have successfully explored saccadic planning (Everling et al. 1997;Richards 2003) and postsaccadic neural responses (Bellebaum et al. 2005;Ossandón et al. 2010). However, most EEG studies of saccadic eye movements are conducted with sparse synthetic visual targets and/or temporally well separated saccades in conditions that do not resemble those that are involved in natural viewing conditions. A variety of fMRI studies of saccadic eye movements, most of which were conducted in more controlled conditions than those associated with natural viewing, have identified various sites of neural activation likely involved in saccadic eye movements (Connolly et al. 2002;Corbetta et al. 1998). However, the low temporal resolution of fMRI makes the study of fast temporal neural dynamics during natural viewing conditions impractical. A general linear least squares or general linear model (GLM...
This paper presents a segmentation method that partly mimics the cognitive-behavioral process used by human subjects to recover motor-temporal information from the image of a handwritten word. The approach does not exploit any thinning or skeletonization procedure, but rather a different type of information is manipulated concerning the curvature function of the word contour. In this way, it is possible to detect the parts of the image where the original odometric information is lost or ambiguous (such as, for example, at an intersection of the handwritten lines) and interpret them to finally recover a part of the original temporal information. The algorithm scans the word, following the natural course of the line, and attempts to reproduce the same movement as executed by the writer during the generation of the word. It segments the cursive trace where the contour shows the slow-down of the original movement (corresponding to the maximum curvature points of the curve). At the end of the scanning process, a temporal sequence of motor strokes is obtained which plausibly composed the original intended movement.
Although most instances of object recognition during natural viewing occur in the presence of saccades, the neural correlates of objection recognition have almost exclusively been examined during fixation. Recent studies have indicated that there are post-saccadic modulations of neural activity immediately following eye movement landing; however, whether post-saccadic modulations affect relatively late occurring cognitive components such as the P3 has not been explored. The P3 as conventionally measured at fixation is commonly used in brain computer interfaces, hence characterizing the post-saccadic P3 could aid in the development of improved brain computer interfaces that allow for eye movements. In this study, the P3 observed after saccadic landing was compared to the P3 measured at fixation. No significant differences in P3 start time, temporal persistence, or amplitude were found between fixation and saccade trials. Importantly, sensory neural responses canceled in the target minus distracter comparisons used to identify the P3. Our results indicate that relatively late occurring cognitive neural components such as the P3 are likely less sensitive to post saccadic modulations than sensory neural components and other neural activity occurring shortly after eye movement landing. Furthermore, due to the similarity of the fixation and saccade P3, we conclude that the P3 following saccadic landing could possibly be used as a viable signal in brain computer interfaces allowing for eye movements.
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