This study examines important developmental differences in patterns of activation in the prefrontal cortex during performance of a Go-No-Go paradigm using functional magnetic resonance imaging (fMRI). Eighteen subjects (9 children and 9 adults) were scanned using gradient echo, echo planar imaging during performance of a response inhibition task. The results suggest four general findings. First, the location of activation in the prefrontal cortex was not different between children and adults, which is similar to our earlier pediatric fMRI results of prefrontal activation during a working memory task (Casey et al., 1995). Second, the volume of activation was significantly greater for children relative to adults. These differences in volume of activation were observed predominantly in the dorsal and lateral prefrontal cortices. Third, although inhibitory processes have typically been associated with more ventral or orbital frontal regions, the current study revealed activation that was distributed across both dorsolateral and orbitofrontal cortices. Finally, consistent with animal and human lesion studies, activity in orbital frontal and anterior cingulate cortices correlated with behavioral performance (i.e., number of false alarms). These results further demonstrate the utility of this methodology in studying pediatric populations.

A functional magnetic resonance imaging (fMRI) study was conducted to determine whether prefrontal cortex (PFC) increases activity in working memory (WM) tasks as a specific result of the demands placed on WM, or to other processes affected by the greater difficulty of such tasks. Increased activity in dorsolateral PFC (DLPFC) was observed during task conditions that placed demands on active maintenance (long retention interval) relative to control conditions matched for difficulty. Furthermore, the activity was sustained over the entire retention interval and did not increase when task difficulty was manipulated independently of WM requirements. This contrasted with the transient increases in activity observed in the anterior cingulate, and other regions of frontal cortex, in response to increased task difficulty but not WM demands. Thus, this study established a double-dissociation between regions responsive to WM versus task difficulty, indicating a specific involvement of DLPFC and related structures in WM function.

In an effort to clarify how deductive reasoning is accomplished, an fMRI study was performed to observe the neural substrates of logical reasoning and mathematical calculation. Participants viewed a problem statement and three premises, and then either a conclusion or a mathematical formula. They had to indicate whether the conclusion followed from the premises, or to solve the mathematical formula. Language areas of the brain (Broca s and Wernicke s area) responded as the premises and the conclusion were read, but solution of the problems was then carried out by non-language areas. Regions in right prefrontal cortex and inferior parietal lobe were more active for reasoning than for calculation, whereas regions in left prefrontal cortex and superior parietal lobe were more active for calculation than for reasoning. In reasoning, only those problems calling for a search for counterexamples to conclusions recruited right frontal pole. These results have important implications for understanding how higher cognition, including deduction, is implemented in the brain. Different sorts of thinking recruit separate neural substrates, and logical reasoning goes beyond linguistic regions of the brain.

In our event-related functional magnetic resonance imaging (fMRI) experiment, participants learned to select between two response options by trial-and-error, using feedback stimuli that indicated monetary gains and losses. The results of the experiment indicate that error responses and error feedback activate the same region of dorsal anterior cingulate cortex, suggesting that this region is sensitive to both internal and external sources of error information.