Abstract
Mastication is the first process in eating behavior.
This process is a very complex set of subprocesses including the size reduction
of food and the lubrication of food particles.
In general, a major problem of the oral process observation analysis is lack of visualization of what goes on.
This fact indicates that by investigating the food states before and after
eating experimentally and numerically, we can understand some of principal
features of mastication processes and propose some phenomenological models.
From physical viewpoints, mastication is regarded as an example of
a far-from-equilibrium phenomenon without any theory based on first
principles.
We believe that it is important to study macroscopic patterns to understand
dynamics of mastication.
We investigated, therefore, the mechanism of food fragmentation by human
mastication through macroscopic pattern formation.
As the first approximation, mastication is regarded as the sequential
fragmentation in the oral cavity.
Therefore, we have investigated the fragment-size distribution produced by
human mastication.
We report that a single lognormal distribution well fits the entire region
for masticated food fragments for several chewing strokes (N. Kobayashi, K. Kohyama, Y. Sasaki and M. Matsushita, J. Phys. Soc. Jpn. 75, 083001 (2006)).
As the number of chewing strokes increased, the fragment-size distribution
changed from the lognormal distribution to a double-size-group structure,
i.e., the smaller group fitted to the lognormal distribution, whereas the
larger group represented the power-law behavior.
The excellent data fitting by the lognormal and power-law distributions implied
that two functions of mastication, a sequential fragmentation with cascade
and randomness, and a lower threshold for fragment size affect the
size distribution of masticated food fragments.
Next, we investigate the scaling property of the shape of food fragments (N. Kobayashi, K. Kohyama, Y. Sasaki and M. Matsushita, J. Phys. Soc. Jpn. 76, 044002 (2007)).
Mastication experiments showed that most fragments have more or less isotropic
shapes which are independent of the number of chewing strokes, whereas larger
fragments than a crossover size have complicated shapes.
Since the crossover size had the structure which was dependent on the number
of chewing strokes, we have tried to propose dynamic scaling hypothesis
analogous to the case of growing self-affine interface.
It was found that the dynamic scaling yields fairly accurate values of the
scaling exponents.
Our results will provide a new observation and insight of not only sequential
fragmentation but also construction for physiological measurement.
This work was supported by the Program for Promotion of Basic Research Activities for Innovative Biosciences (PROBRAIN).
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