Saccadic Localization of Visual Targets by the Very Young Human

1973 ◽  
Author(s):  
Richard N. Aslin ◽  
Philip Salapatek
Keyword(s):  
Visual Targets ◽  
Saccadic Localization

scholarly journals Saccadic localization of visual targets by the very young human infant

1975 ◽  
Vol 17 (3) ◽  
pp. 293-302 ◽  
Author(s):  
Richard N. Aslin ◽  
Philip Salapatek
Keyword(s):  
Human Infant ◽  
Visual Targets ◽  
Saccadic Localization

A Quick Visual Mind Can be a Slow Auditory Mind

2009 ◽  
Vol 56 (1) ◽  
pp. 33-40 ◽  
Author(s):  
Sander Martens ◽  
Addie Johnson ◽  
Martje Bolle ◽  
Jelmer Borst
Keyword(s):  
Attentional Blink ◽  
Task Difficulty ◽  
Human Mind ◽  
Visual Modality ◽  
Present Evidence ◽  
Conscious Level ◽  
Visual Targets ◽  
Concurrent Information

The human mind is severely limited in processing concurrent information at a conscious level of awareness. These temporal restrictions are clearly reflected in the attentional blink (AB), a deficit in reporting the second of two targets when it occurs 200–500 ms after the first. However, we recently reported that some individuals do not show a visual AB, and presented psychophysiological evidence that target processing differs between “blinkers” and “nonblinkers”. Here, we present evidence that visual nonblinkers do show an auditory AB, which suggests that a major source of attentional restriction as reflected in the AB is likely to be modality-specific. In Experiment 3, we show that when the difficulty in identifying visual targets is increased, nonblinkers continue to show little or no visual AB, suggesting that the presence of an AB in the auditory but not in the visual modality is not due to a difference in task difficulty.

scholarly journals Backward masked fearful faces enhance contralateral occipital cortical activity for visual targets within the spotlight of attention

2010 ◽  
Vol 6 (5) ◽  
pp. 639-645 ◽  
Author(s):  
Joshua M. Carlson ◽  
Karen S. Reinke ◽  
Pamela J. LaMontagne ◽  
Reza Habib
Keyword(s):  
Cortical Activity ◽  
Fearful Faces ◽  
Visual Targets

Sensorimotor transformation during eye movements to remembered visual targets

1991 ◽  
Vol 31 (4) ◽  
pp. 693-715 ◽  
Author(s):  
James W. Gnadt ◽  
R. Martyn Bracewell ◽  
Richard A. Andersen
Keyword(s):  
Eye Movements ◽  
Sensorimotor Transformation ◽  
Visual Targets

The cross-modal affective priming effect: Effects of the valence and arousal of primes

2021 ◽  
Vol 49 (12) ◽  
pp. 1-11
Author(s):  
Cheng Kang ◽  
Nan Ye ◽  
Fangwen Zhang ◽  
Yanwen Wu ◽  
Guichun Jin ◽  
...  
Keyword(s):  
Priming Effect ◽  
Affective Priming ◽  
Negative Valence ◽  
Priming Task ◽  
The Cross ◽  
Visual Targets ◽  
Positive And Negative Valence ◽  
Valence And Arousal ◽  
Affective Information

Although studies have investigated the influence of the emotionality of primes on the cross-modal affective priming effect, it is unclear whether this effect is due to the contribution of the arousal or the valence of primes. We explored how the valence and arousal of primes influenced the cross-modal affective priming effect. In Experiment 1 we manipulated the valence of primes (positive and negative) that were matched by arousal. In Experiments 2 and 3 we manipulated the arousal of primes under the conditions of positive and negative valence, respectively. Affective words were used as auditory primes and affective faces were used as visual targets in a priming task. The results suggest that the valence of primes modulated the cross-modal affective priming effect but that the arousal of primes did not influence the priming effect. Only when the priming stimuli were positive did the cross-modal affective priming effect occur, but negative primes did not produce a priming effect. In addition, for positive but not negative primes, the arousal of primes facilitated the processing of subsequent targets. Our findings have great significance for understanding the interaction of different modal affective information.

scholarly journals Influence of visual targets and landmarks on honey bee foraging and waggle dancing

2018 ◽  
Vol 27 (2) ◽  
pp. 349-360 ◽  
Author(s):  
Bahram Kheradmand ◽  
Julian Cassano ◽  
Selena Gray ◽  
James C. Nieh
Keyword(s):  
Honey Bee ◽  
Bee Foraging ◽  
Honey Bee Foraging ◽  
Visual Targets ◽  
Waggle Dancing

Frontal eye field activity preceding aurally guided saccades

1994 ◽  
Vol 71 (3) ◽  
pp. 1250-1253 ◽  
Author(s):  
G. S. Russo ◽  
C. J. Bruce
Keyword(s):  
Spatial Location ◽  
Auditory Target ◽  
Frontal Eye Field ◽  
Visually Guided ◽  
Movement Vector ◽  
Initial Fixation ◽  
Field Activity ◽  
Eye Field ◽  
Movement Field ◽  
Visual Targets

1. We studied neuronal activity in the monkey's frontal eye field (FEF) in conjunction with saccades directed to auditory targets. 2. All FEF neurons with movement activity preceding saccades to visual targets also were active preceding saccades to auditory targets, even when such saccades were made in the dark. Movement cells generally had comparable bursts for aurally and visually guided saccades; visuomovement cells often had weaker bursts in conjunction with aurally guided saccades. 3. When these cells were tested from different initial fixation directions, movement fields associated with aurally guided saccades, like fields mapped with visual targets, were a function of saccade dimensions, and not the speaker's spatial location. Thus, even though sound location cues are chiefly craniotopic, the crucial factor for a FEF discharge before aurally guided saccades was the location of auditory target relative to the current direction of gaze. 4. Intracortical microstimulation at the sites of these cells evoked constant-vector saccades, and not goal-directed saccades. The direction and size of electrically elicited saccades generally matched the cell's movement field for aurally guided saccades. 5. Thus FEF activity appears to have a role in aurally guided as well as visually guided saccades. Moreover, visual and auditory target representations, although initially obtained in different coordinate systems, appear to converge to a common movement vector representation at the FEF stage of saccadic processing that is appropriate for transmittal to saccade-related burst neurons in the superior colliculus and pons.

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