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Brain–Computer Interfaces - Index of

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50 G. Pfurtscheller and C. Neuper<br />

Fig. 2 Relationship between movement type band power changes in the 8–10 Hz (right side) and<br />

the 10–12 Hz frequency bands (left side) over electrode locations C3, Cz and C4. A percentage<br />

band power increase marks ERS, and a decrease reflects ERD. The band power was calculated in<br />

a 500 ms window prior to movement-onset (modified from [26])<br />

widespread over the entire sensorimotor cortex and probably reflects general motor<br />

preparation and attention. Upper mu desynchronization (in the range <strong>of</strong> about<br />

10–12 Hz), in contrast, is topographically restricted and is rather related to taskspecific<br />

aspects. The lower mu frequency component displays a similar ERD with<br />

hand and foot movement, while the higher components display a different pattern<br />

with an ERD during hand and an ERS with foot movement (Fig. 2). This type <strong>of</strong><br />

reactivity <strong>of</strong> different mu components suggests a functional dissociation between<br />

upper and lower mu components. The former displays a somatotopically specific<br />

organization, while the latter is somatotopically unspecific.<br />

Two patterns can develop during BCI training sessions with motor imagery: contralateral<br />

desynchronization <strong>of</strong> upper mu components and a concomitant power<br />

increase (ERS) over the ipsilateral side. In contrast to the bilaterally symmetrical<br />

lower mu ERD, only the upper mu displays an ipsilateral ERS (Fig. 3).<br />

These findings strongly indicate primary motor cortex activity during mental<br />

simulation <strong>of</strong> movement. Hence, we can assume that the pre-movement ERD<br />

and the ERD during motor imagery reflect a similar type <strong>of</strong> readiness or presetting<br />

<strong>of</strong> neural networks in sensorimotor areas. Functional brain imaging studies<br />

(e.g. [32–36]) and transcranial magnetic stimulation (TMS) show an increase<br />

<strong>of</strong> motor responses during mental imagination <strong>of</strong> movements [37], which further<br />

supports involvement <strong>of</strong> the primary sensorimotor cortex in motor imagery.<br />

The observation that movement imagination triggers a significant ipsilateral ERS<br />

along with the contralateral ERD supports the concept <strong>of</strong> antagonistic behavior<br />

<strong>of</strong> neural networks (“focal ERD/surrounding ERS”, [38]) described in the next<br />

section.<br />

In a recent study, several motor imagery tasks were investigated, such as cuebased<br />

left hand, right hand, foot, or tongue motor imagery [39]. Basically, hand<br />

motor imagery activates neural networks in the cortical hand representation area,<br />

which is manifested in the hand area mu ERD. Such a mu ERD was found in all<br />

able-bodied subjects with a clear contralateral dominance. The midcentral ERD, in

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