mechanical designing
The preload arises in the formation of the individual cells,
which try to shorten at the end of the differentiation process. Since this is
not possible in the cellular network, a tensile stress is established
throughout the tissue. Accordingly, the wood in the peripheral areas of the
trunk is shortened in longitudinal direction when cutting a tree across the
fiber.
This pretension status exists in every straight trunk. The
principle of preload also allows trees to purposefully orient their organs or
to change the direction of growth by means of a "Aufkrümmen".
Interestingly, deciduous and coniferous trees follow different strategies.
Deciduous trees on the top of branches and crooked trunks form the so-called
pulling Wood, which, due to a higher tensile preload than in normal wood, pulls
the organ upward. Coniferous trees, on the other hand, form the so-called printwood
on the underside. This tissue tries not to shorten but to extend in
longitudinal direction. Therefore a pressure voltage is created which pushes
the organ upward.
The question of how the conifer can succeed depending on the
need to produce both longitudinal tensile and pressure tensions is of great
interest and has been employed by scientists for quite some time.
The starting point of the considerations for the
clarification of this phenomenon are differences in the nano-and
micro-structure between the respective cell types [12]. While the normal wood
cells of the straight stem have an approximately rectangular cross-section and
a small Zellulosemikrofibrillenwinkel in the dominant cell wall layer (Μ ~ 10
°), typical wooden cells have a circular cross-section and a large
Mikrofibrillenwinkel (Μ ~ 45 °). In addition, in some tree species Lumenseitig
also spiral-shaped columns can be observed (Fig. 4a).
The following simplified assumptions were made for modelling
the stress structure in both cell types: a) The mechanical behaviour of the
cells is mainly determined by the secondary walls; b) The Cellulose Fibrils act
as long, practically unexpandable fibres; c) The matrix shows an elastic
isotropic behavior; and d) A source of the verbund leads to a isotropic volume
increase.
The calculations indicate interesting geometric boundary
conditions, if the cells are differentiated into a source of the cell wall.
Above all, it is crucial whether the cell and tissue structure allows a small
torsion of the individual cell or completely excludes it. This connection is
shown in Figure 4b. The processing of the cell wall results in a rectangle
which remains rectangular when the surface is enlarged, unless torsion is
possible. Since the length of the diagonal must remain constant (unexpandable
cellulose fibril), a maximization of the surface leads to a square. This means
a reduction in longitudinal direction for a Mikrofibrillenwinkel below 45 °.
However, if a small torsion is possible, the rectangle can move into a parallelogram,
which leads to a length increase in longitudinal direction in the case of a
surface magnification.
The "normal" wood cells have an approximately
rectangular cross-section, which suppresses a torsional movement of the single
cell in the cellular compound. Thus, the small Mikrofibrillenwinkel leads to a
longitudinal shortening of the cell when the matrix is swollen. In contrast,
the round cross-section and the spiral-shaped columns could be conducive to
deformation of the pressure wood cells at torsion.
Summary and Outlook
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