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In rodents, hippocampal cell assemblies formed during learning of a navigation task are observed to re-emerge during resting (offline) periods, accompanied by high-frequency oscillations (HFOs). This phenomenon is believed to reflect mechanisms for strengthening newly-formed memory traces. Using magnetoencephalography recordings and a beamforming source location algorithm (synthetic aperture magnetometry), we investigated high-gamma (80–140 Hz) oscillations in the hippocampal region in 18 human participants during inter-trial rest periods in a virtual navigation task. We found right hippocampal gamma oscillations mirrored the pattern of theta power in the same region during navigation, varying as a function of environmental novelty. Gamma power during inter-trial rest periods was positively correlated with theta power during navigation in the first task set when the environment was new and predicted greater performance improvement in the subsequent task set two where the environment became familiar. These findings provide evidence for human hippocampal reactivation accompanied by high-gamma activities immediately after learning and establish a link between hippocampal high-gamma activities and subsequent memory performance.

Highlights • M250 shows amplitude sensitivity to face repetition in adults, but latency sensitivity in children. • Earlier peaks (M100 and M170) show no sensitivity to face repetition in either group. • Face repetition modulates reciprocal connections between OFA and FFA in both groups. • Repetition modulates low-level visual projections to OFA and FFA in adults but only to OFA in children., Electrophysiological studies of adults indicate that brain activity is enhanced during viewing of repeated faces, at a latency of about 250 ms after the onset of the face (M250/N250). The present study aimed to determine if this effect was also present in preschool-aged children, whose brain activity was measured in a custom-sized pediatric MEG system. The results showed that, unlike adults, face repetition did not show any significant modulation of M250 amplitude in children; however children’s M250 latencies were significantly faster for repeated than non-repeated faces. Dynamic causal modelling (DCM) of the M250 in both age groups tested the effects of face repetition within the core face network including the occipital face area (OFA), the fusiform face area (FFA), and the superior temporal sulcus (STS). DCM revealed that repetition of identical faces altered both forward and backward connections in children and adults; however the modulations involved inputs to both FFA and OFA in adults but only to OFA in children. These findings suggest that the amplitude-insensitivity of the immature M250 may be due to a weaker connection between the FFA and lower visual areas.

The cause of stuttering has many theoretical explanations. A number of research groups have suggested changes in the volume and/or function of the striatum as a causal agent. Two recent studies in children and one in adults who stutter (AWS) report differences in striatal volume compared that seen in controls; however, the laterality and nature of this anatomical volume difference is not consistent across studies. The current study investigated whether a reduction in striatal grey matter volume, comparable to that seen in children who stutter (CWS), would be found in AWS. Such a finding would support claims that an anatomical striatal anomaly plays a causal role in stuttering. We used voxel-based morphometry to examine the structure of the striatum in a group of AWS and compared it to that in a group of matched adult control subjects. Results showed a statistically significant group difference for the left caudate nucleus, with smaller mean volume in the group of AWS. The caudate nucleus, one of three main structures within the striatum, is thought to be critical for the planning and modulation of movement sequencing. The difference in striatal volume found here aligns with theoretical accounts of stuttering, which suggest it is a motor control disorder that arises from deficient articulatory movement selection and sequencing. Whilst the current study provides further evidence of a striatal volume difference in stuttering at the group level compared to controls, the significant overlap between AWS and controls suggests this difference is unlikely to be diagnostic of stuttering.

While most normal hearing individuals can readily use prosodic information in spoken language to interpret the moods and feelings of conversational partners, people with congenital amusia report that they often rely more on facial expressions and gestures, a strategy that may compensate for deficits in auditory processing. In this investigation, we used EEG to examine the extent to which individuals with congenital amusia draw upon visual information when making auditory or audio-visual judgments. Event-related potentials (ERP) were elicited by a change in pitch (up or down) between two sequential tones paired with a change in spatial position (up or down) between two visually presented dots. The change in dot position was either congruent or incongruent with the change in pitch. Participants were asked to judge (1) the direction of pitch change while ignoring the visual information (AV implicit task), and (2) whether the auditory and visual changes were congruent (AV explicit task). In the AV implicit task, amusic participants performed significantly worse in the incongruent condition than control participants. ERPs showed an enhanced N2-P3 response to incongruent AV pairings for control participants, but not for amusic participants. However when participants were explicitly directed to detect AV congruency, both groups exhibited enhanced N2-P3 responses to incongruent AV pairings. These findings indicate that amusics are capable of extracting information from both modalities in an AV task, but are biased to rely on visual information when it is available, presumably because they have learned that auditory information is unreliable. We conclude that amusic individuals implicitly draw upon visual information when judging auditory information, even though they have the capacity to explicitly recognize conflicts between these two sensory channels.

Recent evidence shows that hippocampal theta oscillations, usually linked to memory and navigation, are also observed during online language processing, suggesting a shared neurophysiological mechanism between language and memory. However, it remains to be established what specific roles hippocampal theta oscillations may play in language, and whether and how theta mediates the communication between the hippocampus and the perisylvian cortical areas, generally thought to support language processing. With whole-head magnetoencephalographic (MEG) recordings, the present study investigated these questions with two experiments. Using a violation paradigm, extensively used for studying neural underpinnings of different aspects of linguistic processing, we found increased theta power (4–8 ​Hz) in the hippocampal formation, when participants read a semantically incorrect vs. correct sentence ending. Such a pattern of results was replicated using different sentence stimuli in another cohort of participants. Importantly, no significant hippocampal theta power increase was found when participants read a semantically correct but syntactically incorrect sentence ending vs. a correct sentence ending. These findings may suggest that hippocampal theta oscillations are specifically linked to lexical-semantic related processing, and not general information processing in sentence reading. Furthermore, we found significantly transient theta phase coupling between the hippocampus and the left superior temporal gyrus, a hub area of the cortical network for language comprehension. This transient theta phase coupling may provide an important channel that links the memory and language systems for the generation of sentence meaning. Overall, these findings help specify the role of hippocampal theta in language, and provide a novel neurophysiological mechanism at the network level that may support the interface between memory and language.

Background Previous magnetoencephalography (MEG) studies have failed to find a facesensitive, brain response-M170 in children. If this is the case, this suggests that the developmental trajectory of the M170 is different from that of its electrical equivalent, the N170. We investigated the alternative possibility that the child M170 may not be detectable in conventional adult-sized MEG systems. New method Brain responses to pictures of faces and well controlled stimuli were measured from the same four-year-old child with a custom child MEG system and an adult-sized MEG system. Results The goodness of fit of the child's head was about the same over the occipital head surface in both systems, but was much worse over all other parts of the head surface in the adult MEG system compared to the child MEG system. The face-sensitive M170 was measured from the child in both MEG systems, but was larger in amplitude, clearer in morphology, and had a more accurate source localization when measured in the child MEG system. Comparison with existing method The custom-sized child MEG system is superior for measuring the face-sensitive M170 brain response in children than the conventional adult MEG system. Conclusions The present results show that the face-sensitive M170 brain response can be elicited in a four-year-old child. This provides new evidence for early maturation of face processing brain mechanisms in humans, and offers new opportunities for the study of neurodevelopmental disorders that show atypical face processing capabilities, such as autism spectrum disorder.

During bimanual load lifting, the brain not only contends with muscle activations in the load-lifting arm, but also has to pre-emptively modulate muscle activations in the load-bearing arm with temporal precision in order to minimize upward arm deflection. Premature or late inhibition in the load-bearing arm activity would result in augmented arm deflection. Little is currently known about the timing operation of motor systems subserving coordinated, bimanual actions. In this study, we measured neuromagnetic brain activity with whole-head magnetoencephalography while 15 participants performed a bimanual load-lifting task. To investigate neural processes prior to load lifting, a beamformer was applied to 6 contiguous 200 ms time epochs spanning the entire premovement phase of the motor task. The sequence of neural activations, following a signal to lift the weight, was chronologically ordered: firstly, the primary motor cortex contralateral to the load-lifting arm was activated, then the cerebellum, and lastly, the basal ganglia, thalamus and primary-/pre- motor areas contralateral to the load-bearing arm. The current data extend our understanding of the neural underpinnings of bimanual coordination. A model is proposed to account for the central organization of volitional and anticipatory motor control in bimanual load lifting.

Neuroimaging studies have shown that the neural mechanisms of motor imagery (MI) overlap substantially with the mechanisms of motor execution (ME). Surprisingly, however, the role of several regions of the motor circuitry in MI remains controversial, a variability that may be due to differences in neuroimaging techniques, MI training, instruction types, or tasks used to evoke MI. The objectives of this study were twofold: (i) to design a novel task that reliably invokes MI, provides a reliable behavioral measure of MI performance, and is transferable across imaging modalities; and (ii) to measure the common and differential activations for MI and ME with functional magnetic resonance imaging (fMRI) and magnetoencephalography (MEG). We present a task in which it is difficult to give accurate responses without the use of either motor execution or motor imagery. The behavioral results demonstrate that participants performed similarly on the task when they imagined vs. executed movements and this performance did not change over time. The fMRI results show a spatial overlap of MI and ME in a number of motor and premotor areas, sensory cortices, cerebellum, inferior frontal gyrus, and ventrolateral thalamus. MI uniquely engaged bilateral occipital areas, left parahippocampus, and other temporal and frontal areas, whereas ME yielded unique activity in motor and sensory areas, cerebellum, precuneus, and putamen. The MEG results show a robust event-related beta band desynchronization in the proximity of primary motor and premotor cortices during both ME and MI. Together, these results further elucidate the neural circuitry of MI and show that our task robustly and reliably invokes motor imagery, and thus may prove useful for interrogating the functional status of the motor circuitry in patients with motor disorders.

We examined central auditory processing in typically- and atypically-developing readers. Concurrent EEG and MEG brain measurements were obtained from a group of 16 children with dyslexia aged 8–12 years, and a group of 16 age-matched children with normal reading ability. Auditory responses were elicited using 500ms duration broadband noise. These responses were strongly lateralized in control children. Children with dyslexia showed significantly less lateralisation of auditory cortical functioning, and a different pattern of development of auditory lateralization with age. These results provide further evidence that the core neurophysiological deficit of dyslexia is a problem in the balance of auditory function between the two hemispheres.

While stuttering is known to be characterized by anomalous brain activations during speech, very little data is available describing brain activations during stuttering. To our knowledge there are no reports describing brain activations that precede blocking. In this case report we present magnetoencephalographic data from a person who stutters who had significant instances of blocking whilst performing a vowel production task. This unique data set has allowed us to compare the brain activations leading up to a block with those leading up to successful production. Surprisingly, the results are very consistent with data comparing fluent production in stutterers to controls. We show here that preceding a block there is significantly less activation of the left orbitofrontal and inferiorfrontal cortices. Furthermore, there is significant extra activation in the right orbitofrontal and inferiorfrontal cortices, and the sensorimotor and auditory areas bilaterally. This data adds weight to the argument forwarded by Kell et al. (2009) that the best functional sign of optimal repair in stutterering is activation of the left BA 47/12 in the orbitofrontal cortex. Educational objectives: At the end of this activity the reader will be able to (a) identify brain regions associated with blocked vocalization, (b) discuss the functions of the orbitofrontal and inferior frontal cortices in regard to speech production and (c) describe the usefulness and limitations of magnetoencephalography (MEG) in stuttering research.

This study was designed to test two hypotheses about binaural hearing: (1) that binaural cues are primarily processed in the hemisphere contralateral to the perceived location of a sound; and (2) that the two main binaural cues, interaural timing differences and interaural level differences, are processed in separate channels in the auditory cortex. Magnetoencephalography was used to measure brain responses to dichotic pitches – a perception of pitch created by segregating a narrow band of noise from a wider band of noise – derived from interaural timing or level disparities. Our results show a strong modulation of interhemispheric M100 amplitudes by ITD cues. When these cues simulated source presentation unilaterally from the right hemispace, M100 amplitude changed from a predominant right hemisphere pattern to a bilateral pattern. In contrast, ILD cues lacked any capacity to alter the right hemispheric distribution. These data indicate that intrinsic hemispheric biases are large in comparison to any contralaterality biases in the auditory system. Importantly, both types of binaural cue elicited a circa 200 ms latency object-related negativity component, believed to reflect automatic cortical processes involved in distinguishing concurrent auditory objects. These results support the conclusion that ITDs and ILDs are processed by distinct neuronal populations to relatively late stages of cortical processing indexed by the M100. However information common to the two cues seems to be extracted for use in a subsequent stage of auditory scene segregation indexed by the object related negativity. This may place a new bound on the extent to which sound location cues are processed in separate channels of the auditory cortex.

Objective: Conventional whole-head MEG systems have fixed sensor arrays designed to accommodate most adult heads. However arrays optimised for adult brain measurements are suboptimal for research with the significantly smaller heads of young children. We wished to measure brain activity in children using a novel whole-head MEG system custom sized to fit the heads of pre-school-aged children. Methods: Auditory evoked fields were measured from seven 4-year-old children in a 64-channel KIT whole-head gradiometer MEG system. Results: The fit of heads in the MEG helmet dewars, defined as the mean of sensor-to-head centre distances, were substantially better for children in the child helmet dewar than in the adult helmet dewar, and were similar to head fits obtained for adults in a conventional adult MEG system. Auditory evoked fields were successfully measured from all seven children and dipole source locations were computed. Conclusions: These results demonstrate the feasibility of routinely measuring neuromagnetic brain function in healthy, awake pre-school-aged children. Significance: The advent of child-sized whole-head MEG systems opens new opportunities for the study of cognitive brain development in young children.

We investigated event-related oscillatory responses to acoustic stimulation with EEG and MEG measurements of brain function. EEG and MEG measurements were obtained from healthy adults presented with 500 ms segments of broadband noise presented to both ears via insert earphones. The results showed that auditory stimulation resulted in a reduction in beta band activity within 200 to 400 ms after stimulus onset. The magnitude of this effect was markedly larger when listeners actively attended to sounds than when they ignored them. These results support the conclusion that beta-band oscillations are directly influenced by activation of auditory cortex with acoustic stimulation. However these responses are also strongly modulated by attentional and/or motoric factors related to the auditory task.

In this experiment, the oscillatory responses of the MEG were characterized during the observation of four viewing conditions: (a) observation of mouth movements, (b) observation of a non-biological motion stimulus (a mechanical aperture opening and shutting), (c) observation of object-directed mouth movements and (d) observation of speech-like mouth movements. Data were analyzed using synthetic aperture magnetometry (SAM) in three frequency bands, beta (15-35 Hz), gamma (35-70 Hz) and alpha/mu (8-15 Hz). Results showed that observations of biological motion resulted in beta desynchronization over lateral sensorimotor areas, while observations of non-biological motion resulted in a more medial desynchronization, an effect that may be related to the processing of a structured event sequence. Observation of linguistic movements resulted in less alpha/beta desynchronization in posterior brain regions in comparison to biological motion stimuli, suggesting that linguistically-relevant stimuli are processed with different neuronal systems than those recruited by normal action observation. We suggest that non-linguistic actions recruit dorsal systems while linguistic actions engage ventral processing systems. Object-directed movements showed the largest sensorimotor activations, suggesting that, as is the case for observations of hand movements, motoric processing is particularly sensitive to the viewing of goal-directed actions. Taken together, the results indicate that the brain utilizes multiple action encoding strategies, tailored to the function of the observed movement.

Recent electrophysiological studies have shown that the human electroencephalographic mu rhythm is suppressed during the observation of actions performed by other persons, an effect that may be functionally related to the behaviour of so-called "mirror neurons" observed in area F5 of nonhuman primates. Because mirror neuron activity has been reported to be functionally specific to object-oriented actions, the present study was designed to determine if the human mu rhythm also exhibits this property. EEG measurements were obtained from 12 normal subjects while they observed either a precision grip of a manipulandum or an empty grip using the same hand position. Our results showed that the magnitude of the mu rhythm was significantly lower for the object grip condition than for the empty grip condition. These data support the notion that the human mu rhythm indexes a brain system that is functionally comparable to the monkey mirror neuron system. We propose that nonobject-directed actions may result in representational schemas that are either different or less salient than motorically equivalent actions that are directed toward objects.

The time to decide if a letter is normal or backwards (mirror-reversed) increases as the letter is rotated away from the upright. It is widely accepted that this increase in time reflects the mental rotation of the stimulus to the upright orientation in order to determine the mirror-normal status of the stimulus. Although response times tend to be longer for mirrored stimuli than for normal stimuli, the difference is constant across orientation. Little work has been focused on why mirror-image stimuli produce longer response times than normal stimuli. This study examines the question of whether or not mirrored stimuli are rotated in the picture plane at the same time as normal stimuli, and if so, why response times to mirrored stimuli are longer than that for normal stimuli. Both the behavioural and electrophysiological findings suggest that the mirrored stimuli are not only rotated in the picture plane, but that they are subsequently rotated to the normal view. It is this additional rotation that produces, at least in part, the delayed response times for mirror-image stimuli.

Objective : We measured late cortical potentials in a psychophysical procedure for binaural unmasking of a dichotically-embedded pitch. Methods : Late-latency auditory evoked potentials were measured from 128 recording channels in 13 healthy subjects. Control stimuli consisted of 500 ms segments of broadband acoustic noise presented identically to both ears via earphones, evoking a perception of noise localized in the centre of the head. Dichotic pitch stimuli were created by introducing a dichotic delay to a narrow frequency region of the same noise segments, and resulted in a perception of both the centrally-located noise and a right-lateralized pitch. Results : Both stimuli evoked late auditory event-related potentials (ERPs) characterized by a P1-N1-P2 complex of waves between 60 and 180 ms after stimulus onset. ERPs associated with the control and dichotic pitch stimuli showed no amplitude differences for the P1 and N1 waves. ERPs to dichotic pitch stimuli became significantly more negative beginning at a latency around 150 ms, an effect that was maximal between 210 and 280 ms. Topographic mapping showed that this late negativity was lateralized to the left hemisphere. Conclusions : The late negative wave elicited by the dichotic pitch stimulus reflects neural processing that is dependent upon binaural fusion within the auditory system. Significance : The dichotic pitch paradigm may provide a useful tool for the electrophysiological assessment and study of the temporal processing capabilities of the auditory system. This paradigm may also be useful for the study of binaural mechanisms for the perceptual segregation of concurrent sound sources.

To compare mental rotation and mental size transformation, 128-channel EEG was recorded while subjects performed both tasks using random two-dimensional shapes as stimuli. Behavioural results showed significant linear effects of both size transformation and mental rotation on reaction times. Rotation ERPs showed experimental effects at two latencies: a bilateral component distributed over posterior parietal electrodes at a latency of approximately 232–300 ms and a second component at approximately 424–492 ms distributed over right anterior parietal electrodes. The latency and spatial distribution of this second effect is consistent with previous research indicating a functional connection between this component and mental rotation. ERPs for the size-transformation task showed an effect at 180–228 ms distributed bilaterally over occipital–temporal electrodes. These results are consistent with previous hemodynamic imaging studies that show involvement of parietal cortex in mental rotation and also the involvement of BA 19 in size-transformation tasks. However, the superior temporal resolution of the present data indicates that BA 19 activation may occur at a latency that is more likely related to apparent motion than to the size-transformation operation per se.

Objectives : The aim of this study was to examine the N300 and N400 effect to pictures that were semantically incongruous to a prior object name. Based upon theories of object identification, the semantic incongruity was manipulated to occur early or late in the object processing stream. Methods : High-density visual event-related potentials were measured in response to passively viewed black and white line drawings of common objects. Pictures were preceded with an object name at either the basic (categorical) or subordinate (specific) level. The object either matched or mismatched with the name. With subordinate level names, mismatches could be within- or between-category. Results : The N400 effect was found for both basic and subordinate level mismatches. The N400 was found for both the subordinate-within and subordinate-between. Comparison of the scalp distributions between these N400 effects suggested a common effect was found for all conditions. The N300 effect, however, was only found for between-category mismatches, and only when semantic expectations were high in the match baseline (subordinate matches). Conclusions : The findings are consistent with theories of object identification that suggest that objects are initially categorized prior to being identified at more specific levels. The N300 appears to reflect the categorisation while the N400 effect appears to be responsive to all semantic mismatches. Comparison of scalp topographies, functional differences, and different estimated cortical source locations suggest that the N300 and N400 are two distinct semantic effects that reflect aspects of object identification.

Objective : The aim of this study was to obtain a more detailed description of N400 scalp topography than has previously been reported. Methods : High-density (128 channel) visual event-related potentials were measured in an N400 paradigm using semantically incongruous sentence endings. Results : The stimuli elicited an N400 with a centroparietal scalp distribution. In addition, P400s with similar timing and functional characteristics were observed at non-standard recording locations inferior to the temporal lobes. Conclusions : The data are consistent with intracranial evidence for bilateral activation of anterior medial temporal lobe structures. These structures are oriented such that the positive regions of their scalp fields lie largely outside of the area sampled by standard electrode montages. P400s at other non-standard scalp locations, including infraorbital and infraoccipital sites, may reflect volume conduction from the same generators, or activation of non-temporal lobe generators.

Cortical neural networks underlying motor imagery overlaps with motor execution networks and can be consistently activated even by patients with motor weakness. This offers an alternative approach to study motor network activity in ALS. Owing to its high temporal resolution, magnetoencephalography (MEG) is well-suited to localise oscillatory brain wave dysfunction during both executed and motor imagery tasks. This pilot study sought to determine (i) if ALS patients can perform a validated motor imagery task; and (ii) if MEG can be used to measure cortical motor responses from ALS patients longitudinally. Spontaneous brain activity was recorded using a 160 channel whole-head KIT-Macquarie MEG in 4 ALS patients longitudinally over 9 months during a novel hand motor imagery task ( Burianova et al., 2013 ). This task has been shown to consistently activate the primary motor cortex during both executed and imagined movements. Both ALS and control participants achieved high levels of accuracy in the executed and imagined tasks ( > 90%). Beta band desynchronization, an index of motor cortex activity, was observed during both executed and imagined tasks, in both cohorts. Our results showed that motor imagery could be used to probe motor cortical function in ALS patients. This has a distinct advantage over traditional method of investigating cortical function using motor execution tasks because it eliminates the bias associated with progressive muscle weakness. It is feasible to use MEG and motor imagery to (i) identify early biomarkers of cortical involvement in ALS, and (ii) to examine longitudinal effects of progressive motor neuron degeneration on cortical network function.