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In this study, we investigated the continuous EEG fluctuations from alertness to drowsiness in a realistic VR driving environment. Several component clusters exhibited monotonic alpha-band (8-12 Hz) power increase during the transition from alertness to very-slight and slight drowsiness, but remain constant or slight decrease during the extreme drowsiness period. On the other hand, the theta-band (4-7 Hz) power for each component cluster increased monotonically during the transition from slight to extreme drowsiness. Hence, these controversial results may be in part caused by the different drowsiness levels of volunteers.

Additionally, drowsy related alpha and theta rhythm in these component clusters maybe modulated by the same nucleus. Lastly, we compared the EEG between different component clusters diversity of EEG power changes with respect to the transition from alertness to drowsiness and found that alpha power of BLO and OM component were most stable and desirable EEG feature for very-slight and slight drowsiness detection. The theta power of BLO and OM component were the most stable and desirable EEG feature for slight and extreme drowsiness detection.

References

1. K. A. Brookhuis, D. D. Waard, and S. H. Fairclough, “Criteria for driver mpairment,”

Ergonomics, Vol 46, 433-445, 2003.

2. URL: http://www.sleepfoundation.org/.

3. URL: http://en.wikipedia.org/wiki/drowsiness.

4. J. A. Hobson, “Sleep is of the brain, by the brain and for the brain,” Nature, Vol 437, 1254-1256, 2005.

5. C. B. Saper, T. E. Scammell, and J. Lu, “Hypothalamic regulation of sleep and circadian rhythms,” Nature, Vol 437, 1257-1263, 2005.

6. E. D. Adrian, “The basis of sensation,” The Quarterly Review of Biology, Vol 39, 416, 1928.

7. N. D. Volkow, B. Rosen, and L. Farde, “Imaging the living human brain: Magnetic resonance imaging and positron emission tomography,” Proceedings of the National Academy of Sciences, Vol 94, 2787-2788, 1997.

8. A. Parry, and P. M. Matthews, “Functional magnetic resonance imaging (fMRI): A

‘window’ into the brain,” Centre for Functional Magnetic Resonance Imaging of the Brain- Department of Clinical Neurology-University of Oxford, The John Radcliffe Hospital 2002.

9. P. Parikh, and M. E. Tzanakou, “Detecting drowsiness while driving using wavelet transform,” Bioengineering Conference: Proceedings of the IEEE 30th Annual Northeast, 17-18, 2004.

10. M. A. Schier, “Changes in EEG alpha power during simulated driving: a demonstration,”

International Journal of Psychophysiology, Vol 37, 155-162, 2000.

11. S. Makeig and T. P. Jung, “Tonic, Phasic, and Transient EEG Correlates of Auditory Awareness in Drowsiness”, Cognitive Brain Research, Vol 4, 15-25, 1996.

12. S. Makeig and M. Inlow, “Lapse in alertness: coherence of fluctuations in performance and EEG spectrum,” Electroencephalogram and Clinical Neurophysiology, Vol 86, 23-35, 1993.

13. T. P. Jung, S. Makeig, M. Stensom, and T. J. Sejnowski, “Estimating alertness from the EEG power spectrum”, IEEE Transactions on Biomedical Engineering, Vol 44, 60-69 1997.

14 S. Makeig, T. P. Jung, and T. J. Sejnowski, “Awareness during Drowsiness: Dynamics and Electrophysiological Correlates,” Canadian Journal of Experimental Psychology, Vol 54, 266-273, 2000.

15. K. L. Lal and A. Craig, “Driver fatigue: Electroencephalography and psychological assessment,” Psychophysiology, Vol 39, 313-321, 2002.

16. A. Campagne, T. Pebayle, and A. Muzet, “Correlation between driving errors and vigilance level: influence of the driver’s age,” Physiology & Behavior, Vol 80, 515– 524, 2004.

17 J. Beatty, A. Greenberg, W. P. Deibler, and J. O. Hanlon, “Operant control of occipital theta rhythm affects performance, in a radar monitoring task,” Science, Vol 183, 871-873, 1974.

18. C. T. Lin, R. C. Wu, S. F. Liang, W. H. Chao, Y. J. Chen, and T. P. Jung, “EEG-based drowsiness estimation for safety driving using independent component analysis,” Circuits and Systems I: Fundamental Theory and Applications, Vol 52, 2726- 2738, 2005.

19. S. F. Liang, C. T. Lin, R. C Wu, Y. C. Chen, T. Y. Huang, and T. P. Jung, “Monitoring Driver's Alertness Based on the Driving Performance Estimation and the EEG Power Spectrum Analysis,” 27th Annual International Conference of the Engineering in Medicine and Biology Society, 5738-5741, 2005

20 C. T. Lin, S. F. Liang, Y. C. Chen, L. W. Ko, “Driver's drowsiness estimation by combining EEG signal analysis and ICA-based fuzzy neural networks,” IEEE International

Symposium on Circuits and Systems, 2125-2128, 2006.

21 F. Sharbrough, G. E. Chatrian, R. P. Lesser, H. Lüders, M. Nuwer, and T. W. Picton,

“American Electroencephalographic Society Guidelines for Standard Electrode Position Nomenclature,” Journal of Clinical Neurophysiology, Vol 8, 200-202, 1991.

22 J. Malmivuo, and R. Plonsey, Bioelectromagnetism: Principles and applications of bioelectric and bio-magnetic Fields, Oxford University Press, New York, 1995.

23 D. Benton and P. Y. Parker, “Breakfast, blood glucose, and cognition,” The American Journal of Clinical Nutrition, Vol 67, 772S-778S, 1998.

24 J. Hendrix, “Fatal crash rates for tractor-trailers by time of day,” Proceedings of the International Truck and Bus Safety Research and Policy Symposium, 237-250, 2002.

25 H. Ueno, M. Kaneda, and M. Tsukino, “Development of drowsiness detection system,”

Proceedings of the Vehicle Navigation and Information Systems Conference, Vol 31,

15–20, 1994.

26 D. E. Johnson, “Applied multivariate methods for data analysis,” Cole publishing company, California, 1998.

27 C. Jutten, and C. Herault, “Blind separation of sources I. An adaptive algorithm based on neuromimetic architecture,” Signal Process, Vol 24, 1-10, 1991.

28 P. Comon, “Independent component analysis -- A new concept,” Signal Processing, Vol.

36, 287–314, 1994.

29 M. Girolami, “An alternative perspective on adaptive independent component analysis,”

Neural Computation, Vol 10, 2103–2114, 1998.

30 T. W. Lee, M. Girolami, and T. J. Sejnowski, “Independent component analysis using an extended infomax algorithm for mixed sub- and super-Gaussian sources,” Neural Computation, Vol 11, 606-633, 1999.

31 T. P. Jung, C. Humphries, T. W. Lee, S. Makeig, M. J. McKeown, V. Iragui, and T. J.

Sejnowski, “Extended ICA removes artifacts from electroencephalographic recordings,”

Advances in Neural Information Processing Systems, Vol 10, 894-900, 1998.

32 T. P. Jung, S. Makeig, C. Humphries, T. W. Lee, M. J. McKeown, V. Iragui, and T. J.

Sejnowski, “Removing electroencephalographic artifacts by blind source separation,”

Sychophysiology, Vol 37, 163-78. 2000.

33 T. P. Jung, S. Makeig, W. Westerfield, J. Townsend, E. Courchesne, and T. J. Sejnowski,

“Analysis and visualization of single-trial event-related potentials,” Human Brain Mapping, Vol 14, 166-85. 2001.

34 A. Yamazaki, T. Tajima, and K. Matsuoka, “Convolutive independent component analysis of EEG data,” Annual Conference on the Society of Instrument and Control Engineering, Vol 2, 1227-1231.2003.

35 A. Meyer-Base, D. Auer, and A. Wismueller, “Topographic independent component analysis for fMRI signal detection,” Proceedings of the International Joint Conference on Neural Networks, Vol 1, 601-605, 2005.

36 M. Naganawa, Y. Kimura, K. Ishii, K. Oda, K. Ishiwata, and A. Matani, “ Extraction of a plasma time-activity curve from dynamic brain pet images based on independent component analysis,” IEEE Transactions on Biomedical Engineering, Vol 52, 201–210, 2005.

37 R. Liao, J. L. Krolik, and M. J. McKeown, “An information-theoretic criterion for intrasubject alignment of FMRI time series: motion corrected independent component analysis,” IEEE Transactions on Medical Imaging, Vol 24, 29-44, 2005.

38 A. J. Bell, and T. J. Sejnowski, “An information-maximization approach to blind separation and blind deconvolution,” Neural Computation, Vol 7, 1129–1159, 1995.

39 T. P. Jung, S. Makeig, M. Westerfield, J. Townsend, E. Courchesne, and T. J. Sejnowski,

“Removal of eye activity artifacts from visual event-related potentials in normal and clinical subjects,” Clinical Neurophysiology, 1745-1758, 2000.

40 T. P. Jung, S. Makeig, C. Humphries, T. W. Lee, M. J. Mckeown, V. Iragui, and T. J.

Sejnowski, “Removing electroencephalographic artifacts by blind source separation”

Psychophysiology, Vol 37, 163-178, 2000.

41 J. Onton, M. Westerfield, J. Townsend, and S. Makeig, “Imaging human EEG dynamics using independent component analysis,” Neuroscience and Biobehavioral Reviews, Vol 30, 808–822, 2006.

42 M. F. Bear, B. W. Connors, and M. A. Paradiso, “Neuroscience: Exploring the brain”

Lippincott Williams and Wilkins, 2001.

43 L. D. Gennaro, M. Ferrara and, M. Bertini, “The Boundary between wakefulness and sleep:

quantitative electroencephalographic changes during the sleep onset period,”

Neuroscience, Vol 107, 1-11, 2001.

44 S. Makeig, T. P. Jung, and T. J. Sejnowski, “Awareness during drowsiness: dynamics and electrophysiological correlates,” Canadian Journal of Experimental Psychology, Vol 54, 266-273, 2000.

45 URL: http://en.wikipedia.org/wiki/K-means_algorithm.

46. R. Conradta, U. Brandenburga, T. Penzela, J. Hasanb, A. VaÈrric, and J. H. Peter,

“Vigilance transitions in reaction time test: a method of describing the state of alertness more objectively,” Clinical Neurophysiology, Vol 110, 1499-1509, 1999.

47 Y. Harrison, J. A. Horne, “Occurrence of microsleeps during daytime sleep onset in normal subjects,” Electroencephalogram Clinical Neurophysiology, Vol 98, 411–416.

1996.

48 M. L. Thomas, H. C. Sing, G. Belenky, H. H. Holcomb, H. S. Mayberg, R. F. Dannals, H.

N. Wagner, D. R. Thorne , K. A. Popp, L. M. Rowland, A. B. Welsh, S. M. Balwinski and D.P. Redmond, “Neural basis of alertness and cognitive performance impairments during sleepiness II. Effects of 48 and 72 h of sleep deprivation on waking human regional brain activity,” Thalamus & Related Systems, Vol 2, 199-229, 2003.

49 G. Robin, S. John, E. Jerome, and C. Mark, “Simultaneous EEG and fMRI of the alpha

rhythm,” Brain Imaging, Vol 13, 2487-2492, 2002.

50 G. Pfurtscheller, A. Stancak, and C. H. Neuper, “Event-related synchronization (ERS) in the alpha band-an electrophysiological correlate of cortical idling: A review,”

International Journal of Psychophysiology, Vol 24, 39-46, 1996.

51 J. L. Cantero, M. Atienza, and R. M. Salas “Human alpha oscillations in wakefulness, drowsiness period, and REM sleep: different electroencephalographic phenomena within the alpha band,” Neurophysiology Clinical, Vol 32, 54-71, 2002.

52 F. H. Lopes, V. Lierop, C. F. Schrijer, and W. S. V. Leeuwen, “Organization of thalamic and cortical alpha rhythms: spectra and coherences,” Electroencephalography Clinical Neurophysiology, Vol 35, 627-39, 1973.

53 F. H. Lopes, J. E. Vos, J. Mooibroek, and A. V. Rotterdam, “Relative contributions of the intracortical and thalamo-cortical processes in the generation of alpha rhythms, revealed by partial coherence analysis,” Electroencephalogram Clinical Neurophysiology, Vol 50 449-56, 1980.

54 M. Steriade, “Sleep oscillations and their blockage by activating systems,” Journal of Psychiatry and Neuroscience, Vol 19, 54-58, 1994.

55 J. L. Cantero, M. Atienza, R. Stickgold, M. J. Kahana, J. R. Madsen and B. Kocsis,

“Sleep-Dependent theta Oscillations in the Human Hippocampus and Neocortex,” The Journal of Neuroscience, Vol 26, 10897-10903, 2003.

56 T. D. Albright, “Direction and orientation selectivity of neurons in visual area MT of the macaque,” Journal of Neurophysiology, Vol 52, 1106-1130, 1984.

57 G. A. Orban, H. Kennedy and J. Bullier, “Velocity sensitivity and direction selectivity of neurons in areas V1 and V2 of the monkey: influence of eccentricity,” Journal of Neurophysiology, Vol 56, 462-480, 1986.

58 M. L. Posner, “The attention system of the human brain,” Annual Review of Neuroscience, Vol 13, 25-42, 1990.

59 S. Corchs, and G. Deco, “Feature-based attention in human visual cortex: simulation of fMRI data,” NeuroImage, Vol 21, 36–45, 2004.

60 O. J. Braddick, and J. O'Brian, “Brain areas sensitive to visual motion,” Perception, Vol 30, 61-72, 2001.

61 M. Leonardo, J. Fieldman, N. Sadato, G. Campbell, V. Ibañez, L. Cohen, M. P. Deiber, P. Jezzard, T. Pons, R. Turner, D. L. Bihan, and M. Hallett, “A functional magnetic resonance imaging study of cortical regions associated with motor task execution and motor ideation in humans,” Human Brain Mapping, Vol 3, 83 – 92, 2004.

62 D. Marianne, and B. Thomas, “Brain activation studies on visual-vestibular and ocular motor interaction,” Current Opinion in Neurology, Vol 13, 13-18, 2000.

63 C. A. Porro, M. P. Francescato, V. Cettolo, M. E. Diamond, P. Baraldi, C. Zuiani, M.

Bazzocchi, and P. E. Prampero, “Primary Motor and Sensory Cortex Activation during Motor Performance and Motor Imagery: A Functional Magnetic Resonance Imaging Study,” The Journal of Neuroscience, Vol 16, 7688–7698, 1996.

64 H. J.Freund, “Premotor area and preparation of movement,” Review of Neuroscience, Vol 146, 543-7, 1990.

65 C. Buchel, O. Josephs, G. Rees, R. Turner, C. D. Frith and K. J. Friston, “The functional anatomy of attention to visual motion: A functional MRI stud,” Brain, Vol 121, 1281–1294, 1998.

66 L. Torsvall and T. Akerstedt, “Sleepness on the job: continuous measured EEG changes in train driver,” Electroencephalogram Clinical Neurophysiology, Vol 66, 502-511, 1987.

67 G. Keckluno and T. Akersteot, “Sleepness in long distance truck driving: an ambulatory EEG study of night driving,” Ergonomics, Vol 36, 1007-1017, 1993.

68 H. J. Eoh, M. K. Chung and S. H. Kim,“Electroencephalographic study of drowsiness in simulated driving with sleep deprivation,” International Journal of Industrial Ergonomics, Vol 35, 307-320, 2005.

Table I. The number of subjects for each cluster

BLO OM FCM CM CPM LCP RCP

n / N 13/16 8/16 9/16 8/16 9/16 7/16 7/16 BLO OM FCM CM CPM LCP RCP

n / N 13/16 8/16 9/16 8/16 9/16 7/16 7/16

N represented the number of total subjects and n represented the number of subjects for each cluster.

Table II. Summary of the component index of subjects in each cluster

Table III. The peak frequency of grand mean baseline power spectra

Table IV. The percentage of subjects with high correlation between powers in time series (correlation coefficient > 0.6) of the different components

RCP

The alpha power had high correlation between BLO, OM, CPM, LCP and RCP component and the theta power had high correlation between BLO, OM, CM, CPM, LCP and RCP components for the great part of subjects.

Table V. The R-square values between grand mean of EEG power fluctuations and first-order linear regression line

Very slight drowsiness Slight drowsiness Extreme drowsiness

0.69

Very slight drowsiness Slight drowsiness Extreme drowsiness

0.69

Very slight drowsiness Slight drowsiness Extreme drowsiness

Table VI. The slop of first-order linear regression line

Very slight drowsiness Slight drowsiness Extreme drowsiness

0.06

Very slight drowsiness Slight drowsiness Extreme drowsiness

0.06

Very slight drowsiness Slight drowsiness Extreme drowsiness

Table VII. The mean value of standard deviation

Very slight drowsiness Slight drowsiness Extreme drowsiness

0.24

Very slight drowsiness Slight drowsiness Extreme drowsiness

0.24

Very slight drowsiness Slight drowsiness Extreme drowsiness

Fig. 2-1: The block diagram of the VR-based driving simulation environment with the EEG-based physiological measurement system.

Fig. 2-2: The VR-based four-lane highway scenes are projected into 360° surround screen with seven projectors.

Fig. 2-3: The 32 channel EEG cap.

Fig. 2-4: The International 10-20 system of electrode placement. (A) The lateral view, (B) The top view [22].

Deviation Onset

Reaction Time Cruising

(Trajectory)

Deviation

Response Offset

Response Onset

Cruising (Trajectory) Res pon se

Time Deviation

Onset

Reaction Time Cruising

(Trajectory)

Deviation

Response Offset

Response Onset

Cruising (Trajectory) Res pon se

Time

Fig. 2-5: An example of the deviation event. The car cruised with a fixed velocity of 100 km/hr on the VR-based highway scene and it was randomly drifted either to the left or to the right away from the cruising position with a constant velocity. The subjects were instructed to steer the vehicle back to the center of the cruising lane as quickly as possible.

Fig. 2-6: The digitized highway scene. The width of highway is equally divided into 256 units and the width of the car is 32 units.

Fig. 2-7: An example of the driving performance that represented by the digitized vehicle deviation trajectories.

0 30 60 90 120 150 250

200

150

100

50

0

Time (sec)

Driving Performance

0 30 60 90 120 150 250

200

150

100

50

0

Time (sec)

Driving Performance

Fig. 3-1: The utilized EEG signals processing procedure.

Fig. 3-2: An example of the scalp topographies of ICA weighting matrix W by spreading each w into the plane of the scalp corresponding to the ij j ICA components based on th International 10-20 system.

1s Amplitude (dB)Amplitude (dB)Amplitude (dB)Amplitude (dB)

IC Activations Scalp Map Power

Spectrum

Amplitude (dB)Amplitude (dB)Amplitude (dB)Amplitude (dB)

IC Activations Scalp Map Power

Spectrum

Fig. 3-3: Time course signals, scalp maps and power spectra of some typical independent components representing different types of artifacts and EEG sources. (A) The eye blink component. (B) The horizontal eye movement component. (C) The temporal muscle component. (D) The channel noise component. (E) The parietal EEG source

Median

Fig. 3-4: The smoothed EEG power spectral analysis procedure. The EEG data of the extracted ICA components was first accomplished using a 750-point Hanning window with 250-point overlap. Windowed 750-point epochs were further subdivided into several 125-point subwindows using the Hanning window again with 25-point step. Each 125-point frame was extended to 256 points by zero-padding to calculate its power spectrum by using a 256-point fast Fourier transform (FFT),,resulting in power-spectrum density estimation with a frequency resolution near 1 Hz.

0 10 20 30 40

Fig. 3-5: Local driving error.

Subject 1

Fig. 3-6: Component clustering analysis. The components of all volunteer were clustered semi-automatically based on the gradients values, [Gxi Gyi], of the component scalp maps. K-mean algorithm was utilized for clustering.

Data point

A lpha P o w e r (dB )

Time (s)

Lo cal D riv in g E rro r Local D ri v ing E rror Al p h a Po w e r ( d B)

Step 1

Step 2

Step 3 Baseline removal

Sorting the Error

Smoothing

Original LDE trajectory Sorts the LDE

Data point

A lpha P o w e r (dB )

Time (s)

Lo cal D riv in g E rro r Local D ri v ing E rror Al p h a Po w e r ( d B)

Step 1

Step 2

Step 3 Baseline removal

Sorting the Error

Smoothing

Data point

A lpha P o w e r (dB )

Time (s)

Lo cal D riv in g E rro r Local D ri v ing E rror Al p h a Po w e r ( d B)

Step 1

Step 2

Step 3 Baseline removal

Sorting the Error

Smoothing

Original LDE trajectory Sorts the LDE

Fig. 3-7: An example of the sorted spectral analysis. The left subplot of Fig 3-6 is a subject’s original LDE trajectory (the blue line) and the corresponding alpha power changes (the red line). The right subplot sorts the LDE values in ascending order and shows the transient alpha powers corresponding to the sorted LDE values. It can be found that the alpha power is increasing at the beginning and will decrease at the latter when LDE values are ascending.

Fig. 4-1: Equivalent dipole source locations and scalp maps for Bi-Lateral Occipital (BLO, the left column), Occipital-Midline (OM, the middle column), and Frontal-Central-Midline (FCM, the right column) independent component clusters. (Upper panels) 3-D dipole source locations (colored spheres) and their projections onto an average brain image. Dipole spheres of different volunteers are represented by different colors. (Lower panels) Scalp maps of the clustered components. The label above each scalp map represents the index of the volunteer and the component index of the volunteer.

Fig. 4-2: Equivalent dipole source locations and scalp maps for Central-Midline (CM, the left column), Central-Parietal-Midline (CPM, the middle left column), Left-Central-Parietal (LCP, the (middle right column) and Right-Central-Parietal (RCP, the right column) independent component clusters. (Upper panels) 3-D dipole source locations (colored spheres) and their projections onto an average brain image. Dipole spheres of different volunteers are represented by different colors. (Lower panels) Scalp maps of the clustered components. The label above each scalp map represents the index of the volunteer and the component index of the volunteer.

Frequency (Hz)

Power (dB)

LDE

Alpha Power (dB) Theta Power (dB)

Local Driving Error

Power (dB)

(A) (B)

(C) Frequency (Hz) (D)

Power (dB)

Local Driving Error

Frequency (Hz) Frequency (Hz)

Power (dB)

LDE

Alpha Power (dB) Theta Power (dB)

Local Driving Error

Power (dB)

(A) (B)

(C) Frequency (Hz) (D)

Power (dB)

Local Driving Error Frequency (Hz)

Fig. 4-3: Activations of the Bi-Lateral Occipital (BLO) cluster. (A) The grand mean of the scalp map and the baseline power spectral. (B) The grand mean log power spectral density changes accompanying with the sorted local driving error (LDE) in ascending order. (C, D) show the transient alpha and theta powers corresponding to the ascending LDE values, respectively. (A, C, D) the solid lines represent the grand mean power spectra and the dotted lines represent the variance of the power spectra. These notifications will be utilized in the illustrations of the other component clusters. The peak frequency of the baseline power spectral is near 10 Hz for BLO component cluster. When the LDE values increase from 0 to 40, the alpha power (8~12Hz) has increasing the sustaining activations. The theta power (4~7Hz) increases monotonically from low LDE to high LDE.

Frequency (Hz)

Power (dB)

LDE

Alpha Power (dB) Theta Power (dB)

Local Driving Error Local Driving Error

Power (dB)

(A) (B)

(C) Frequency (Hz) (D)

Power (dB)

Frequency (Hz)

Power (dB)

LDE

Alpha Power (dB) Theta Power (dB)

Local Driving Error Local Driving Error

Power (dB)

(A) (B)

(C) Frequency (Hz) (D)

Power (dB)

Fig. 4-4: Activations of the Frontal Central Midline (FCM) cluster. (A) The grand mean of the scalp map and the baseline power spectral. (B) The grand mean log power spectral density changes accompanying with the sorted local driving error (LDE) in ascending order. (C, D) show the transient alpha and theta powers corresponding to the ascending LDE values, respectively. (A, C, D) the solid lines represent the grand mean power spectra and the dotted lines represent the variance of the power spectra. The peak frequency of the baseline power spectral baseline is near 5 Hz for FCM component cluster. The powers of the alpha band and the theta band increase monotonically from low LDE to high LDE.

Frequency (Hz)

Power (dB)

LDE

Alpha Power (dB) Theta Power (dB)

Local Driving Error Local Driving Error

Power (dB)

(A) (B)

(C) Frequency (Hz) (D)

Power (dB)

Frequency (Hz)

Power (dB)

LDE

Alpha Power (dB) Theta Power (dB)

Local Driving Error Local Driving Error

Power (dB)

(A) (B)

(C) Frequency (Hz) (D)

Power (dB)

Fig. 4-5: Activations of the Central Midline (CM) cluster. (A) The grand mean of the scalp map and the baseline power spectral. (B) The grand mean log power spectral density changes accompanying with the sorted local driving error (LDE) in ascending order. (C, D) show the transient alpha and theta powers corresponding to the ascending LDE values, respectively. (A, C, D) the solid lines represent the grand mean power spectra and the dotted lines represent the variance of the power spectra. The peak frequency of the baseline power spectral is near 7 Hz for CM component cluster. Similar to the BLO cluster, the LDE values increase from 0 to 40, the alpha power (8~12Hz) has increasing the sustaining activations. The theta power (4~7Hz) increases monotonically from low LDE to high LDE.

Frequency (Hz)

Power (dB)

LDE

Alpha Power (dB) Theta Power (dB)

Local Driving Error Local Driving Error

Power (dB)

(A) (B)

(C) Frequency (Hz) (D)

Power (dB)

Frequency (Hz)

Power (dB)

LDE

Alpha Power (dB) Theta Power (dB)

Local Driving Error Local Driving Error

Power (dB)

(A) (B)

(C) Frequency (Hz) (D)

Power (dB)

Fig. 4-6: Activations of the Central Parietal Midline (CPM) cluster. (A) The grand mean of the scalp map and the baseline power spectral. (B) The grand mean log power spectral density changes accompanying with the sorted local driving error (LDE) in ascending order. (C, D) show the transient alpha and theta powers corresponding to the ascending LDE values, respectively. (A, C, D) the solid lines represent the grand mean power spectra and the dotted lines represent the variance of the power spectra. The peak frequency of the baseline power spectral is near 10 Hz for CPM component cluster. Similar to the BLO cluster, the LDE values increase from 0 to 40, the alpha power (8~12Hz) has increasing the sustaining activations. The theta power (4~7Hz) increases monotonically from low LDE to high LDE.

Frequency (Hz)

Power (dB)

LDE

Alpha Power (dB) Theta Power (dB)

Local Driving Error Local Driving Error

Power (dB)

(A) (B)

(C) Frequency (Hz) (D)

Power (dB)

Frequency (Hz)

Power (dB)

LDE

Alpha Power (dB) Theta Power (dB)

Local Driving Error Local Driving Error

Power (dB)

(A) (B)

(C) Frequency (Hz) (D)

Power (dB)

Fig. 4-7: Activations of the Left Central Parietal (LCP) cluster. (A) The grand mean of the scalp map and the baseline power spectral. (B) The grand mean log power spectral density changes accompanying with the sorted local driving error (LDE) in ascending order. (C, D) show the transient alpha and theta powers corresponding to the ascending LDE values, respectively. (A, C, D) the solid lines represent the grand mean power spectra and the dotted lines represent the variance of the power spectra. The peak frequency of the baseline power spectral is near 10 Hz for LCP component cluster. Similar to the BLO cluster, the LDE values increase from 0 to 40, the alpha power (8~12Hz) has increasing the sustaining activations.

The theta power (4~7Hz) increases monotonically from low LDE to high LDE.

Frequency (Hz)

Power (dB)

LDE

Alpha Power (dB) Theta Power (dB)

Local Driving Error Local Driving Error

Power (dB)

(A) (B)

(C) Frequency (Hz) (D)

Power (dB)

Frequency (Hz)

Power (dB)

LDE

Alpha Power (dB) Theta Power (dB)

Local Driving Error Local Driving Error

Power (dB)

(A) (B)

(C) Frequency (Hz) (D)

Power (dB)

Fig. 4-8: Activations of the Right Central Parietal (RCP) cluster. (A) The grand mean of the scalp map and the baseline power spectral. (B) The grand mean log power spectral density changes accompanying with the sorted local driving error (LDE) in ascending order. (C, D) show the transient alpha and theta powers corresponding to the ascending LDE values, respectively. (A, C, D) the solid lines represent the grand mean power spectra and the dotted lines represent the variance of the power spectra. The peak frequency of the baseline power spectral is near 10 Hz for RCP component cluster. Similar to the BLO cluster, the LDE values

Fig. 4-8: Activations of the Right Central Parietal (RCP) cluster. (A) The grand mean of the scalp map and the baseline power spectral. (B) The grand mean log power spectral density changes accompanying with the sorted local driving error (LDE) in ascending order. (C, D) show the transient alpha and theta powers corresponding to the ascending LDE values, respectively. (A, C, D) the solid lines represent the grand mean power spectra and the dotted lines represent the variance of the power spectra. The peak frequency of the baseline power spectral is near 10 Hz for RCP component cluster. Similar to the BLO cluster, the LDE values

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