Ian T Harrison

Publications (2)10.43 Total impact

• Article: Inattention blindness to motion in middle temporal area.

  Ian T Harrison, Katherine F Weiner, Geoffrey M Ghose
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  ABSTRACT: Subjects naturally form and use expectations to solve familiar tasks, but the accuracy of these expectations and the neuronal mechanisms by which these expectations enhance behavior are unclear. We trained animals (Macaca mulatta) in a challenging perceptual task in which the likelihood of a very brief pulse of motion was consistently modulated over time and space. Pulse likelihood had dramatic effects on behavior: unexpected pulses were nearly invisible to the animals. To examine the neuronal basis of such inattention blindness, we recorded from single neurons in the middle temporal (MT) area, an area related to motion perception. Fluctuations in how reliably MT neurons both signaled stimulus events and predicted behavioral choices were highly correlated with changes in performance over the course of individual trials. A simple neuronal pooling model reveals that the dramatic behavioral effects of attention in this task can be completely explained by changes in the reliability of a small number of MT neurons.
  Journal of Neuroscience 05/2013; 33(19):8396-410. · 7.11 Impact Factor
• Article: Temporal precision of neuronal information in a rapid perceptual judgment.

  Geoffrey M Ghose, Ian T Harrison
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  ABSTRACT: In many situations, such as pedestrians crossing a busy street or prey evading predators, rapid decisions based on limited perceptual information are critical for survival. The brevity of these perceptual judgments constrains how neuronal signals are integrated or pooled over time because the underlying sequence of processes, from sensation to perceptual evaluation to motor planning and execution, all occur within several hundred milliseconds. Because most previous physiological studies of these processes have relied on tasks requiring considerably longer temporal integration, the neuronal basis of such rapid decisions remains largely unexplored. In this study, we examine the temporal precision of neuronal activity associated with a rapid perceptual judgment. We find that the activity of individual neurons over tens of milliseconds can reliably convey information about sensory events and was well correlated with the animals' judgments. There was a strong correlation between sensory reliability and the correlation with behavioral choice, suggesting that rapid decisions were preferentially based on the most reliable sensory signals. We also find that a simple model in which the responses of a small number of individual neurons (<5) are summed can completely explain behavioral performance. These results suggest that neuronal circuits are sufficiently precise to allow for cognitive decisions to be based on small numbers of action potentials from highly reliable neurons.
  Journal of Neurophysiology 01/2009; 101(3):1480-93. · 3.32 Impact Factor