The anterior temporal lobe (ATL) sits at the confluence of auditory, visual, olfactory, transmodal, and limbic processing hierarchies. In keeping with this anatomical heterogeneity, the ATL has been implicated in numerous functional domains, including language, semantic memory, social cognition, and facial identification. One question that has attracted considerable discussion is whether the ATL contains a mosaic of differentially specialized areas or whether it provides a domain-independent amodal hub. In the current study, based on task-free fMRI in right-handed neurologically intact participants, we found that the left lateral ATL is interconnected with hubs of the temporosylvian language network, including the inferior frontal gyrus and middle temporal gyrus of the ipsilateral hemisphere and, to a lesser extent, with homotopic areas of the contralateral hemisphere. In contrast, the right lateral ATL had much weaker functional connectivity with these regions in either hemisphere. Together with evidence that has been gathered in lesion-mapping and event-related neuroimaging studies, this asymmetry of functional connectivity supports the inclusion of the left ATL within the language network, a relationship that had been overlooked by classic aphasiology. The asymmetric domain selectivity for language of the left ATL, together with the absence of such an affiliation in the right ATL, is inconsistent with a strict definition of domain-independent amodal functionality in this region of the brain.

We used the P300 component to investigate how changes in local context influenced the ability to detect target stimuli. Local context was defined as the occurrence of a short predictive series of stimuli before delivery of a target event. EEG was recorded in 12 subjects during auditory and visual sessions. Stimuli were presented in the center of the auditory and visual field and consisted of 15% targets (1000 Hz tone or downward facing triangle) and 85% of equal amounts of three types of standards (1500, 2000, and 2500 Hz tones or triangles facing left, upward, and right). Recording blocks consisted of targets preceded by either randomized sequences of standards or by sequences including a three-standard predictive sequence signaling the occurrence of a subsequent target event. Subjects pressed a button in response to targets. Peak target P300 (P3b) amplitude and latency were evaluated for targets after predictive and nonpredictive sequences using conventional averaging and a novel single-trial analysis procedure. Reaction times were shorter for predictable targets than for nonpredicted targets. P3b latency was shorter for predicted targets than for nonpredictive targets, and there were no significant P3b amplitude differences between predicted and random targets, as determined by both conventional averaging and single-trial analysis. Comparable effects on amplitude and latency were observed in both the auditory and visual modalities. The results indicate that local context has differential effects on P3b amplitude and latency, and exerts modality-independent effects on cognitive processing.

Response time (RT) is an important behavioral measure of the overall efficacy of sensorimotor processing and is known to vary significantly from trial to trial. Past work on how stimulus evoked cortical responses contribute to RT variability has helped delineate the stages of neuronal information processing. Much less is known about how the state of the brain immediately preceding the stimulus onset (prestimulus) affects RT. We addressed this problem by analyzing data from three macaque monkeys trained to perform a visuomotor pattern discrimination task. Local field potentials were recorded from up to 16 bipolar surface-to-depth electrodes widely distributed over one cerebral hemisphere in each monkey. The degree of linear correlation between RT and prestimulus spectral power was determined over a wide range of frequencies. In the prefrontal cortex, prestimulus power in the beta range (14–30 Hz) was negatively correlated with RT in two monkeys, suggesting a possible role of activity in this frequency range in the mediation of top-down control of visuomotor processing. In the sensorimotor cortex, prestimulus power in the beta range was positively correlated with RT in two monkeys, consistent with the hypothesis that oscillations in this range support the maintenance of steady-state motor output. In visual occipital and temporal lobe areas, prestimulus power in the alpha/low beta range (8–20 Hz) showed positive correlations with RT in three monkeys, possibly reflecting a spatially specific disengagement of visual anticipatory attention. Through measurement of prestimulus spectral coherence, it was further determined that sites showing similar patterns of correlation between spectral power and RT were also linked together in synchronized networks.