Chapter
2
Cellular
Partitions
The
notion
of
discrete model introduced
in the
previous chapter relies strongly
on a
decomposition
of
objects
into
a finite set of
connected nodes. However,
as
pointed
out in figure
(1.4),
such nodes connectivities
are not
sufficient
to
describe
without
ambiguity
the
topology
of
these objects.
In
this
chapter,
we
will
see how
cellular
partitions
can
achieve this goal
in a
completely general
way, whatever the object (manifold/non-manifold) or the dimension of the
embedding space
(ID,
2D,
...,
nD).
2.1
Introduction
It is
well known
that
complex biological objects, also called organs, consist
of
sets
of
adjacent "biological
3D
cells," which
are
structured
to
respect
the
external
and
internal boundaries
of
these objects.
It can be
observed
that
•
from
a
mathematical
point
of
view,
each
3D
cell
is in
fact
an
element
of
volume
which
can be
transformed
into
a 3D
ball,
continuously,
and
•
each
3D
cell
holds
attributes
consisting
of
information
attached,
for
example,
to its
genes.
Similarly,
as
shown
in
figures
(2.1),
(2.35),
(3.17),
and
(3.23),
the
subsur-
face
can be
decomposed into "geological
3D
cells" having attributes (physical
properties)
and
bounded
by
geological horizons
and
faults.
As
suggested
in
figure
(2.2),
the
same approach
can be
used
to
decompose
a
geological cross
section
or a
geological
map
into
2D
cells (which
can be
transformed into
a 2D
ball,
continuously).
Over
the
past
decade,
this
cellular paradigm
has
been used
by
several
computers scientists
as a
template
for
modeling
the
topology
of
complex
ob-
jects (e.g.,
see
[35,
37, 66, 67, 68,
134,
181]).
A
complete presentation
of the
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