fast Fourier transform of the EEG time series and analysing transformed data at
the following frequency bands: delta wave (0.5 to 3.5 Hz), theta wave (4 to 7.5
Hz), alpha wave (8 to 13 Hz) and beta wave (14 to 30 Hz). Some main findings
from the above studies include that there seem to be no significant delta wave
changes associated with fatigue, theta and alpha wave activities increase significantly
during fatigue, but where, in the cortex, these changes occur is still to be probed,
and the association between beta wave activity and fatigue remains unclear. [29]
probed into the delta and beta frequency bands to verify the existence of power-law
scaling, usually realised in the form of 1/f-power spectrum. The authors of [29] used
irregularly resampled auto-spectral analysis in conjunction with ARMA modelling
to quantify the 1/f-component of magnetoencephalography, electroencephalography
and electrocorticography (MEG/EEG/ECoG) power spectra in the low (0.1 to 2.5
Hz) and high (5 to 100 Hz) frequency bands. Their findings confirm power-law
scaling in the MEG/EEG/ECoG in a more refined form of 1/f
β
-power spectrum.
Furthermore, the results follow a spatial pattern in the sense that, in the higher
frequencies, steeper slopes are present in posterior areas. In contrast, for the lower
frequencies, steeper slopes are present in the frontal cortex.
Many complex systems in nature, from earthquakes to avalanches, are charac-
terised by scale invariance, which is usually identified by a power-law distribution
of variables such as event duration or the waiting time between events [6, 23]. The
1/f-noise is considered to be a footprint of such systems. 1/f-frequency scaling is
the behaviour of a system near critical points. As such, one commonly associates
self-organised critical states of a natural system with 1/f-frequency scaling [23].
Apart from MEG/EEG/ECoG, temporal signals displaying power-law scaling have
been observed in many works on the nervous system at various spatial scales, from
membrane potentials [16] to functional magnetic resonance imaging [20]. Despite
its potential importance, the physiological mechanism which generates power-law
scaling is still not well understood, and its significance for brain activity remains
controversial [10]. It has been argued [9] that the existence of power-law scaling
indicates that the brain is in a state of self-organised criticality. [8] pointed out
that, alternatively, 1/f-frequency scaling may be due to the diffusion of EEG sig-
nals through various extracellular media such as cerebrospinal fluid, dura matter,
cranium muscle and skin. Such a heterogeneous medium induces a combination of
resistive effects, due to the flow of current in a conductive fluid, and capacitive ef-
fects due to the high density of membranes. In [7], the authors showed theoretically
that 1/f-power spectra could be created by ionic current flow in such a complex
network of resistors and capacitors with random values.
This paper will contribute a new angle to the debate on the cause and detec-
tion of power-law scaling of brain wave activity. We focus on the quantification
of the cause, and subsequent response of the system, which models and interprets
the heterogeneity of the brain cortex. Our starting point is the construction of a
mathematical model of global brain wave activity based on all EEG measurements.
Instead of modelling wave activities at various locations or regions of the brain, we
will consider the evolution of the random field representing EEG over the entire cor-
tical surface. The model takes the form of a stochastic delay-differential equation
(SDDE) for this random field. Its two main components, the fractional diffusion
operator and the delay operator capture respectively the two critical features of
the system: the response due to the heterogeneous medium and the response to an
2
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The copyright holder for this preprintthis version posted August 4, 2020. ; https://doi.org/10.1101/2020.08.03.234120doi: bioRxiv preprint