2009 Ninth IEEE International Conference on Bioinformatics and Bioengineering
˘˘˚ˀ˵˴̆˸˷ʳ˦̃˴̇˼˴˿ʳˡ˴̉˼˺˴̇˼̂́ʳ˘̆̇˼̀˴̇˼̂́ʳ˼́ʳ˴ʳ˩˼̅̇̈˴˿ʳ˥˸˴˿˼̇̌ʳ˗̅˼̉˼́˺ʳ˘́̉˼̅̂́̀˸́̇
Chin-Teng Lin1,2,3, Fu-Shu Te-Chung Chiou1,3, Li-Wei Jeng-Ren
Gramann4
Ko1,2
Yang1,3
1
Brain Research Center
Department of Electrical Engineering,
National Chiao Tung University
Hsinchu 300, Taiwan
e-mail: ctlin@mail.nctu.edu.tw
yfs0606@hotmail.com
2
Klaus
4
3
Department of Computer Science
National Chiao Tung University
Hsinchu 300, Taiwan
e-mail: xk4nk4.cs97g@nctu.edu.tw
lwko@mail.nctu.edu.tw
Swartz Center for Computational
Neuroscience
University of California San Diego
La Jolla, CA, 92093-0961 USA
e-mail: duann@sccn.ucsd.edu
klaus@sccn.ucsd.edu
lateral hemisphere including frontal, parietal, pre-motor,
occipital, and temporal areas revealed an association
with spatial navigation [4-6]. Moreover, the neuropsychological studies suggested the functional dissociation
between the use of allocentric and egocentric reference
frames [7-9].
In our previous study [20], we found that EEG spectrum power changes were significantly different between
the navigation strategy groups. Subjects who preferred to
use the allocentric spatial representation showed stronger
activation in occipital area during path integration whereas subjects using the egocentric reference frames
showed stronger activation in parietal area during path
integration.
The aim of this study is to investigate the difference
of EEG dynamics on navigation performance. We first
distinguished subjects using the egocentric reference
frames from subjects using the allocentric reference
system during navigation by a spatial tunnel task [9].
Then we estimated their navigation performance during
the task respectively. The tunnel task was built in a 3D
virtual reality based driving-simulation environment.
Since there was no extra landmarks in the tunnel, subjects’ navigation strategies were not biased by the environment and therefore we could classify subjects into
two different navigation strategy groups according to
their use of cognitive reference frames while passing
through the tunnel. The 32-channel EEG activities were
recorded during subjects navigated in the tunnel and
responded to the homing direction selections and homing
angular estimation. EEG signals were processed and
revealed in the spectro-temporal domain. Effects of the
navigation strategy and performance on neural rhythms
were compared and assessed in details.
The paper was organized as follows. We introduced
the apparatus and materials of the study in Section II and
explored the EEG dynamics with innovative methods by
combining Independent Component Analysis (ICA),
time-frequency spectral and power spectrum analysis in
Section III. Section IV showed the performance-predictive EEG activities associated with the use
of egocentric reference frames. And finally the discussion and conclusions were presented in Section V.
Abstract—The aim of this study is to investigate the difference of EEG dynamics on navigation performance. A
tunnel task was designed to classify subjects into allocentric
or egocentric spatial representation users. Despite of the
differences of mental spatial representation, behavioral
performance in general were compatible between the two
strategies subjects in the tunnel task. Task-related EEG
dynamics in power changes were analyzed using independent component analysis (ICA), time-frequency and
non-parametric statistic test. ERSP image results revealed
navigation performance-predictive EEG activities which is
is expressed in the parietal component by source reconstruction. For egocentric subjects, comparing to trails with
well-estimation of homing angle, the power attenuation at
the frequencies from 8 to 30 Hz (around alpha and beta
band) was stronger when subjects overestimated homing
directions, but the attenuated power was decreased when
subjects were underestimated the homing angles. However,
we did not found performance related brain activities for
allocentric subjects, which may due to the functional dissociation between the use of allo- and egocentric reference
frames.
Keywords —spatial navigation, allocentric, egocentric,
reference frame, electroencephalograph (EEG)
I. INTRODUCTION
Spatial navigation is a crucial ability for living, since
way-finding and environment exploration always happens in our daily life. Spatial navigation is a complex
task which requires to integrate information from different sensory inputs and to construct the spatial representation of the environment. According to the computation of reference of frames, there are two classes of
internal spatial representation systems: the allocentric
representation system and the egocentric representation
system [1-3].
In the egocentric reference system, the spatial location
of an object is specified with respect to the navigator or
observer. The spatial representation of an object depends
on the position or orientation of the observer and the
representation changes along with the observer's position
or orientation. On the other hand, people who prefer to
use an allocentric reference frame describe the spatial
location of an object with respect to features or landmarks of the environment [3]. Visuospatial navigation is
a task that involves complex cognitive functions which
employ multiple brain regions. Brain activations in bi978-0-7695-3656-9/09 $25.00 © 2009 IEEE
DOI 10.1109/BIBE.2009.65
Duann1,4,
II. EXPERIMENTAL APPARATUS
A.
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Subjects
contained about 45 trails. Between two sessions, subjects
could take rest for about 5-10 minutes.
Eighteen right-handed subjects were paid to participate in this research (age: 20-28 years, mean: 25
years). None of subjects had a history of neurological or
psychiatric disease and without drug or alcohol abuse.
Subjects gave their written informed consent to participate in the study, which was approved by the Institutional Review Broad of Taipei Veterans General Hospital.
B.
EEG Recording
The physiological data acquisition used 32 unipolar
sintered Ag/AgCl EEG electrodes. All the electrodes
were placed in an elastic cap according to the international 10-20 system. EEG data were recorded with the
Scan NuAmps Express system (Compumedics Ltd.,
VIC, Australia) and digitized at 1000 Hz and 16-bit
quantization level.
C.
Fig. 1. The episodes of virtual tunnel environment. (A): the entrance;
(B): the forthright segment; (C): the meander segment; (D): the exit; (E):
the cue for indicating homing direction and (F): the cue for indicating
homing angle.
III. DATA ANALYSIS
Stimuli and Procedure
The subjects sat comfortably in a car which was
mounted in the center of a dimmed quiet room. Five
projection screens circularly surround the car with a
distance of 100 cm and provide 206° frontal field of view
(FOV), and 40° back FOV to construct a virtual driving
environment. All virtual scenery and physical motion
were built and simulated by the tool of World Tool Kit
(WTK). Subjects were required to perform a tunnel task
[11] and instructed to keep relax and without movement
as possible during the task.
We used the VR based tunnel-driving environment
to investigate the EEG dynamics in spatial navigation.
Animations of passages through a 3D virtual tunnel
consisting of a turning segment which is between the two
straight segments were presented on the screen to simulate automatic car driving with a constant velocity (see
Fig. 1). The VR scene only provided subjects with visual
flows of spatial translation and rotation. No other landmarks or references existed in the tunnel scenery to affect
subject’s navigation strategy. The turning segment of the
tunnel scene was randomly turned left or right in degree
of 30, 60, and 90. Subjects were required to keep the
track of their implied virtual 3-D position with respect to
their starting position during passage. At the end of each
passage, a three dimensional homing arrow was appeared in the empty space in front of subject and subjects
were required to indicate the homing direction by
pressing the left or right buttons and the arrowhead was
pointed roughly in the direction of the tunnel origin. The
selection of the homing direction was associated with the
subject’s navigation strategy, the use of the reference
frame. For example, for a right turn task, subjects with
allocentric reference fame would indicate that the original entrance was in his left hand-side. Once the subject
pressed the button to point the homing direction, the
arrow started to rotate from 0 degree until subjects
pressed the button again and the arrow was stopped and
pointed to the more correct homing angle. Each subject
was asked to practice the task around 5 min to familiar
with the task. Each subject was required to complete 4
20-minute sessions in the experiment and each session
A.
Analysis of the Behavior Data
Subjects were first classified into allocentric subject and
egocentric subject according to their pointing direction.
Three subjects were excluded due to their inconsistency
on pointing direction (<90% of total trials). To investigate the task performance, signed pointing error was
analyzed across all subjects. Trails of signed pointing
error exceeding three times of standard deviation were
simply removed as outliers. Trials with left turn were
simply mirrored, to collapse task performance across left
and right turns. Then we classified all trails into three
classes according to its signed pointing error. Trails with
their pointing error in the range of ±0.5 standard deviation were labeled as well-estimation. Trials with their
signed pointing error less than -0.5 and greater than 0.5
standard deviation were labeled as under-estimation and
over-estimation.
B.
EEG Analysis
The continuous EEG signals were analyzed by the means
of MATLAB (The Mathworks, Inc.) and the open source
EEGLAB toolbox (http://sccn.ucsd.edu/eeglab). The
EEG signals were first down sampled to 250Hz for data
compression and filtered to 0.5-50Hz by a low-pass filter
with a cut-off frequency of 50 Hz to remove the line
noise (60 Hz and its harmonic) and a high-pass filter with
a cut-off frequency of 0.5 Hz to remove the DC drift.
Signal intervals containing electrode noise, large bursts
of muscle artifacts were identified by visual inspection
using the EEGLAB visualization tool and eliminated to
enhance the signal to noise ratio.
C.
Independent Component Analysis
Independent component analysis (ICA) methods
have been extensively applied to the blind source separation problem and also demonstrated that was a suitable
solution to the problem of EEG source segregation,
identification, and localization. [13-15]. EEG signals
were transformed into statistical maximally independent
components (ICs) accounting for eye blinks, other eye
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movements, or muscle artifacts according to their scalp
maps and activity profiles. Only brain activity related ICs
were selected for further analysis.
D.
Event Related Spectral Perturbations (ERSP)
ERSP is a kind of time-frequency analysis, which
was first proposed by Makeig [16], can reveal those
time-locked but not necessary phase-lock event related
activities. ERSP analysis transforms time-course signal
into spectral-temporal domain by short term fast Fourier
transform (FFT). Log power spectra were computed and
then were normalized by subtracting the baseline
(straight tunnel segment) log mean power spectral. Significance of deviations from power spectral baseline was
assessed by bootstrapping, a nonparametric permutation-based statistical method. Non-significant points
were masked as zero; only significant (p<0.05) perturbations were remained.
Fig.3: The pointing error of egocentric subjects (A): turning degree of
30, (B): turning degree of 60, (C): turning degree of 90.
B.
IV. RESULT
Results demonstrated that the navigation performance related changes on brain activities were located in
the parietal component of the egocentric subjects. For
egocentric subjects, comparing to trials with
well-estimation of homing angle, the power attenuation
at the frequencies from 8 to 30 Hz (around alpha and beta
band) was stronger when subjects overestimated homing
directions, but the attenuated power was decreased when
subjects were underestimated the homing angles. However, we did not found performance related brain activities for allocentric subjects, which may due to the functional dissociation between the use of allo- and egocentric reference frames. Fig. 3 shows the grand mean ERSP
images of parietal component of egocentric subjects.
Results showed that alpha and beta band powers slightly
decreased during passing through the tunnel. Since the
duration of tunnel passage is less than 10 sec, ERSP
images here only showed the changes at the first 10 sec
of the trails.
A total of 20 subjects completely finished this experiment. 11 of them were categorized into allocentric
subjects, and 7 participants were categorized into egocentric subjects. The rest three subjects were not able to
be classified into any category because their homing
direction selections varied trials by trials
A.
The Performance related brain activity
Behavior Performance
Fig. 2 illustrates the distributions of allocentric
subjects’ signed pointing error of all trials among three
cases of tunnel degree (30°: 6.94±7.04, 60°: 0.01±9.60,
90°: -5.21±14.20). Fig. 3 shows the distributions of
egocentric subjects’ pointing error of all trials among
three cases of tunnel degree (30°: 3.84±7.30, 60°:
-4.29±9.43, 90°: -11.51±12.72). The pointing errors
were in the range of [-20, 50] degrees. The mean pointing
error revealed an overall bias to overestimate small and
to underestimate large required pointing angles in both
allocentric and egocentric subjects.
Fig. 2: The pointing error of allocentric subjects (A): turning degree of
30, (B): turning degree of 60, (C): turning degree of 90.
Fig. 4: The grand mean of the ERSP images of egocentric subject in
parietal component for tunnel degree of 30. Top panel: ERSP of under-estimation. Middle panel: ERSP of well-estimation. Bottom panel:
ERSP of over-estimation.
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Fig. 5: The grand mean of the ERSP images of egocentric subject in
parietal component for tunnel degree of 60. Panels were as Fig. 4.
Fig. 6: The grand mean of the ERSP images of egocentric subject in
parietal component for tunnel degree of 90. Panels were as Fig. 4.
V. DISCUSSION AND CONCLUSION
There has little direct experiment evidence for the
correlation between the task performance and EEG data.
Based on our past study, we designed an experiment to
see whether there is a correlation between task performance and EEG data.
In this study, the relationship between the grand mean
of ERSP of parietal component of egocentric subject and
task performance is discovered. Alpha band power
slightly decreased when subjects passing through the
tunnel turn. Moreover, it is evident that the alpha band
power strongly decreased in underestimated the homing
angles among three cases of tunnel degree. However, we
did not found performance related brain activities for
allocentric subjects, which may due to the functional
dissociation between the use of allo- and egocentric
reference frames.
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