How infant-directed actions enhance infants’ attention,learning, and exploration: Evidence from EEG and computational modeling

When teaching infants new actions, parents tend to modify their movements. Infants prefer these infant-directed actions (IDAs) over adult-directed actions and learn well from them. Yet, it remains unclear how parents’ action modulations capture infants’ attention. Typically, making movements larger than usual is thought to draw attention. Recent findings, however, suggest that parents might exploit movement variability to highlight actions. We hypothesized that variability in movement amplitude rather than higher amplitude is capturing infants’ attention during IDAs. Using EEG, we measured 15-month-olds’ brain activity while they were observing action demonstrations with normal, high, or variable amplitude movements. Infants’ theta power (4–5 Hz) in fronto-central channels was compared between conditions. Frontal theta was significantly higher, indicating stronger attentional engagement, in the variable compared to the other conditions. Computational modelling showed that infants’ frontal theta power was predicted best by how surprising each movement was. Thus, surprise induced by variability in movements rather than large movements alone engages infants’ attention during IDAs. Infants with higher theta power for variable movements were more likely to perform actions successfully and to explore objects novel in the context of the given goal. This highlights the brain mechanisms by which IDAs enhance infants’ attention, learning, and exploration.     

Effects of component length and of the transitions among components in multiple schedules

Pigeons received equal variable-interval reinforcement during presentations of two line-orientation stimuli while five other orientations appeared in extinction. Component duration was 30 seconds for all orientations and the sequence was arranged so that each orientation preceded itself and each other orientation equally often. The duration of one component (0°) was shortened to 10 seconds and the other (90°) was lengthened to 50 seconds. All animals showed large increases in response rate in the shortened component and this increase was recoverable after an interpolated condition in which all components were again 30 seconds in duration. This effect was replicated in a second experiment in which component duration was changed from 150 seconds to 50 seconds and 250 seconds. An examination of local contrast effects during the first experiment showed that the shortened component produced local contrast during subsequent presentations of the lengthened component, just as would a component associated with more frequent reinforcement. When the presentation sequence was changed so that the lengthened component was always followed by the shortened component, response rates generally increased during the lengthened component. When the sequence was arranged so that the shortened component always preceded the longer component, response rate decreased in the former. These effects, as well as the increases in response rate following change in component length, seem not to be the product of local contrast effects among components.     

Local contrast and maintained generalization.

Pigeons received variable-interval reinforcement for key pecking during presentations of horizontal and vertical line-orientation stimuli, while pecks during five intermediate orientations were extinguished. Lowest peck rates were observed during presentations of negative stimuli adjacent to the positive orientations while peck rate during 45 degrees (the intermediate negative orientation) was relatively high, i.e., there were negative contrast shoulders. When peck rates were manipulated in the positive orientations, peck rate in neithboring orientations changed in the opposite direction. Contrast shoulders faded after prolonged training. A second type of contrast, local contrast, was correlated with similarity of preceding stimulus and different average peck rates during different stages of the discrimination process. The data suggest that sequential local contrast accompanying the formation of a discrimination contributes to the form of generalization gradients. Blough's model of stimulus control predicts the changes in gradient form described here, but may not accurately depict the underlying process responsible for gradient form.