Switching behavior based on multiple rules is a fundamental ability of flexible behavior. Although interactions among the frontal, parietal, and sensory cortices are necessary for such flexibility, little is known about the neural computations concerning contextdependent information readouts. Here, we provide evidence that neurons in the lateral intraparietal area (LIP) accumulate relevant information preferentially depending on context. We trained monkeys to switch between direction and depth discrimination tasks and analyzed the buildup activity in the LIP depending on task context. In accordance with behavior, the rate of buildup to identical visual stimuli differed between tasks and buildup was prominent only for the stimulus dimension relevant to the task. These results indicate that LIP neurons accumulate relevant information depending on context to decide flexibly where to move the eye, suggesting that flexibility is, at least partly, implemented in the form of temporal integration gain control.

Neurons in the primary visual cortex (V1) detect binocular disparity by computing the local disparity energy of stereo images. The representation of binocular disparity in V1 contradicts the global correspondence when the image is binocularly anticorrelated. To solve the stereo correspondence problem, this rudimentary representation of stereoscopic depth needs to be further processed in the extrastriate cortex. Integrating signals over multiple spatial frequency channels is one possible mechanism supported by theoretical and psychophysical studies. We examined selectivities of single V4 neurons for both binocular disparity and spatial frequency in two awake, fixating monkeys. Disparity tuning was examined with a binocularly correlated random-dot stereogram (RDS) as well as its anticorrelated counterpart, whereas spatial frequency tuning was examined with a sine wave grating or a narrowband noise. Neurons with broader spatial frequency tuning exhibited more attenuated disparity tuning for the anticorrelated RDS. Additional rectification at the output of the energy model does not likely account for this attenuation because the degree of attenuation does not differ among the various types of disparity-tuned neurons. The results suggest that disparity energy signals are integrated across spatial frequency channels for generating a representation of stereoscopic depth in V4.

Numerous psychophysical studies have described perceptual learning as long-lasting improvements in perceptual discrimination and detection capabilities following practice. Where and how long-term plastic changes occur in the brain is central to understanding the neural basis of perceptual learning. Here, neurophysiological research using non-human primates is reviewed to address the neural mechanisms underlying visual perceptual learning. Previous studies have shown that training either has no effect on or only weakly alters the sensitivity of neurons in early visual areas, but more recent evidence indicates that training can cause long-term changes in how sensory signals are read out in the later stages of decision making. These results are discussed in the context of learning specificity, which has been crucial in interpreting the mechanisms underlying perceptual learning. The possible mechanisms that support learning-related plasticity are also discussed.