Numerous studies have established that visual working memory has a limited capacity, and that capacity increases during childhood. However, debate continues over the source of capacity limits and its developmental increase. Simmering (2008) adapted a computational model of spatial cognitive development, the Dynamic Field Theory, to explain not only the source of capacity limitations but also the developmental mechanism. According to the model, capacity is limited by the balance between excitation and inhibition that maintains multiple neural representations simultaneously. Moreover, development is implemented according to the Spatial Precision Hypothesis, which proposes that excitatory and inhibitory connections strengthen throughout early childhood. Critically, these changes in connectivity result in increasing precision and stability of neural representations over development. Here we test this developmental mechanism by probing children’s memory in a single-item change detection task. Results confirmed the model’s predictions, providing further support for this account of visual working memory capacity development.

During free viewing, faces attract gaze and induce specific fixation patterns corresponding to the facial features. This suggests that neurons encoding the facial features are in the causal chain that steers the eyes. However, there is no physiological evidence to support a mechanistic link between face encoding neurons in high-level visual areas and the oculomotor system. In this study, we targeted the middle face patches of inferior temporal (IT) cortex in two macaque monkeys using an fMRI localizer. We then utilized muscimol microinjection to unilaterally suppress IT neural activity inside and outside the face patches and recorded eye movements while the animals free viewing natural scenes. Inactivation of the face selective neurons altered the pattern of eye movements on faces: the monkeys found faces in the scene but neglected the eye ipsilateral to the inactivation hemisphere. These findings reveal the causal contribution of the high-level visual cortex in eye movements.

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