Illusory motion can be generated by successively flashing a stationary visual stimulus in two spatial locations separated by several degrees of visual angle. In appropriate conditions, the apparent motion is indistinguishable from real motion: The observer experiences a luminous object traversing a continuous path from one stimulus location to the other through intervening positions where no physical stimuli exist. The phenomenon has been extensively investigated for nearly a century but little is known about its neurophysiological foundation. Here we present images of activations in the primary visual cortex in response to real and apparent motion. The images show that during apparent motion, a path connecting the cortical representations of the stimulus locations is filled in by activation. The activation along the path of apparent motion is similar to the activation found when a stimulus is presented in real motion between the two locations.

In visual search, inefficient performance of human observers is typically characterized by a steady increase in reaction time with the number of array elements—the so-called set-size effect. In general, set-size effects are taken to indicate that processing of the array elements depends on limited-capacity resources, that is, it involves attention. Contrasting theories have been proposed to account for this attentional involvement, however. While some theories have attributed set-size effects to the intervention of serial attention mechanisms, others have explained set-size effects in terms of parallel, competitive architectures. Conclusive evidence in favor of one or the other notion is still lacking. Especially in view of the wide use of visual search paradigms to explore the functional neuroanatomy of attentional mechanisms in the primate brain, it becomes essential that the nature of the attentional involvement in these paradigms be clearly defined at the behavioral level. Here we report a series of experiments showing that highly inefficient search indeed recruits serial attention deployment to the individual array elements. In addition, we describe a number of behavioral signatures of serial attention in visual search that can be used in future investigations to attest a similar involvement of serial attention in other search paradigms. We claim that only after having recognized these signatures can one be confident that truly serial mechanisms are engaged in a given visual search task, thus making it amenable for exploring the functional neuro-anatomy underlying its performance.

Visual comparison between different-sized objects with respect to shape can be done by encoding one of the objects as a mental image, transforming the image to the size format of the other object, and then testing for a match (Bundesen, C., & Larsen, A. [1975]. Visual transformation of size. Journal of Experimental Psychology: Human Perception and Performance, 1 , 214-220). To identify the brain structures implicated in mental transformation of size, we measured the distribution of regional cerebral blood flow (rCBF) by positron emission tomography (PET) in 12 normal subjects who compared random stimulus patterns with respect to shape regardless of variations in size in a one-back match-to-sample paradigm. Each subject was PET-scanned 12 times during repetitive injections of H 2 15 O. In one condition (three scans), all stimulus patterns were small. In a second condition (three scans), all stimuli were large. In the third condition (six scans), the stimuli alternated between small and large. Mental transformation of size should occur in the alternating-size condition but not in the fixed-size conditions. As expected, behavioral measures (reaction time [RT], d ', β) were nearly the same for the two fixed-size conditions but mean RT was longer and d ' smaller in the alternating-size condition. Changes in rCBF specific to mental transformation of size were estimated by contrasting the alternating-size with the fixed-size conditions by use of statistical parametric mapping (SPM96) at a threshold of p < .05 corrected for multiple comparisons. The detected brain structures implicated in mental transformation of size were primarily located in the dorsal pathways, comprising structures in the occipital, parietal, and temporal transition zone (predominantly in the left hemisphere), posterior parietal cortex (bilaterally), area MT/V5 (left), and vermis (bilaterally). Contrasts between the two fixed-size conditions showed significant effects in only the occipital cortex.