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Traditionally, studies of the visual system of nonhuman primates have investigated neurons while the animal fixates a target in a static environment. Clearly, this is not what our everyday life is like; neither the environment nor we are stationary while we act in our world. On the contrary, we constantly move our eyes or limbs. Here we review a number of recent studies describing the brain in a more realistic mode of operation.

While reading this text, your eyes jump from word to word. Yet you are unaware of the motion this causes on your retina; the brain somehow compensates for these displacements and creates a stable percept of the world. This compensation is not perfect; perisaccadically, perceptual space is distorted. We show that this distortion can be traced to a representation of retinal position in the medial temporal and medial superior temporal areas. These cells accurately represent retinal position during fixation, but perisaccadically, the same cells distort the representation of space. The time course and magnitude of this distortion are similar to the mislocalization found psychophysically in humans. This challenges the assumption in many psychophysical studies that the perisaccadic retinal position signal is veridical.

In monkeys, posterior parietal and premotor cortex play an important integrative role in polymodal motion processing. In contrast, our understanding of the convergence of senses in humans is only at its beginning. To test for equivalencies between macaque and human polymodal motion processing, we used functional MRI in normals while presenting moving visual, tactile, or auditory stimuli. Increased neural activity evoked by all three stimulus modalities was found in the depth of the intraparietal sulcus (IPS), ventral premotor, and lateral inferior postcentral cortex. The observed activations strongly suggest that polymodal motion processing in humans and monkeys is supported by equivalent areas. The activations in the depth of IPS imply that this area constitutes the human equivalent of macaque area VIP.

Complex actions often can be decomposed into sequences of individual movements. Primate medial motor areas (SMA and pre-SMA) have been shown to be key players in the concert of such sequential actions. In this issue of Neuron, Lu and Ashe show for the first time that neurons in primate M1—the ultimate output stage of cortex—have anticipatory activity related to specific movement sequences. These findings challenge the traditional view of M1 as being a simple module for generating movements.

Traditionally, studies of the visual system of nonhuman primates have investigated neurons while the animal fixates a target in a static environment. Clearly, this is not what our everyday life is like; neither the environment nor we are stationary while we act in our world. On the contrary, we constantly move our eyes or limbs. Here we review a number of recent studies describing the brain in a more realistic mode of operation.

Our actions, and those of others, are often partly obscured from view. This complicates the sensory inputs that guide motor actions. In this issue of Neuron, Umilità and colleagues demonstrate that “mirror neurons” in ventral premotor cortex respond when monkeys observe hidden, but inferred, actions.